EP2130931A1 - Method for producing aluminum alloy thick plate and aluminum alloy thick plate - Google Patents
Method for producing aluminum alloy thick plate and aluminum alloy thick plate Download PDFInfo
- Publication number
- EP2130931A1 EP2130931A1 EP08722912A EP08722912A EP2130931A1 EP 2130931 A1 EP2130931 A1 EP 2130931A1 EP 08722912 A EP08722912 A EP 08722912A EP 08722912 A EP08722912 A EP 08722912A EP 2130931 A1 EP2130931 A1 EP 2130931A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- aluminum alloy
- percent
- mass
- content
- less
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229910000838 Al alloy Inorganic materials 0.000 title claims abstract description 546
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 89
- 238000010438 heat treatment Methods 0.000 claims abstract description 150
- 238000000034 method Methods 0.000 claims abstract description 134
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 129
- 238000005266 casting Methods 0.000 claims abstract description 117
- 238000002844 melting Methods 0.000 claims abstract description 99
- 230000008018 melting Effects 0.000 claims abstract description 99
- 238000001914 filtration Methods 0.000 claims abstract description 81
- 239000012535 impurity Substances 0.000 claims abstract description 41
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 38
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 31
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 31
- 229910052742 iron Inorganic materials 0.000 claims abstract description 17
- 238000011282 treatment Methods 0.000 claims description 129
- 238000005520 cutting process Methods 0.000 claims description 46
- 238000009499 grossing Methods 0.000 claims description 42
- 239000013078 crystal Substances 0.000 claims description 27
- 238000005498 polishing Methods 0.000 claims description 8
- 238000000227 grinding Methods 0.000 claims description 7
- 229910052725 zinc Inorganic materials 0.000 abstract description 17
- 229910052748 manganese Inorganic materials 0.000 abstract description 12
- 229910052804 chromium Inorganic materials 0.000 abstract description 11
- 229910052802 copper Inorganic materials 0.000 abstract description 8
- 229910052719 titanium Inorganic materials 0.000 abstract description 8
- 229910052726 zirconium Inorganic materials 0.000 abstract description 7
- 239000000956 alloy Substances 0.000 description 606
- 229910045601 alloy Inorganic materials 0.000 description 603
- 238000002048 anodisation reaction Methods 0.000 description 96
- 239000011777 magnesium Substances 0.000 description 93
- 238000011156 evaluation Methods 0.000 description 92
- 238000012360 testing method Methods 0.000 description 89
- 239000011572 manganese Substances 0.000 description 76
- 230000000052 comparative effect Effects 0.000 description 69
- 239000000463 material Substances 0.000 description 69
- 239000011701 zinc Substances 0.000 description 64
- 239000011651 chromium Substances 0.000 description 45
- 229910000765 intermetallic Inorganic materials 0.000 description 45
- 239000010936 titanium Substances 0.000 description 44
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 41
- 239000010949 copper Substances 0.000 description 38
- 230000035882 stress Effects 0.000 description 31
- 229910052749 magnesium Inorganic materials 0.000 description 22
- 238000005098 hot rolling Methods 0.000 description 16
- 229910018134 Al-Mg Inorganic materials 0.000 description 15
- 229910018467 Al—Mg Inorganic materials 0.000 description 15
- 229920006395 saturated elastomer Polymers 0.000 description 15
- 230000000694 effects Effects 0.000 description 13
- 229910018131 Al-Mn Inorganic materials 0.000 description 12
- 229910018461 Al—Mn Inorganic materials 0.000 description 12
- 229910018571 Al—Zn—Mg Inorganic materials 0.000 description 12
- 238000012545 processing Methods 0.000 description 12
- 229910021365 Al-Mg-Si alloy Inorganic materials 0.000 description 11
- 230000007547 defect Effects 0.000 description 11
- 239000007789 gas Substances 0.000 description 11
- 238000005096 rolling process Methods 0.000 description 11
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- 239000001257 hydrogen Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 8
- 230000002411 adverse Effects 0.000 description 7
- 229910052755 nonmetal Inorganic materials 0.000 description 7
- 238000009825 accumulation Methods 0.000 description 6
- 230000032683 aging Effects 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 150000002843 nonmetals Chemical class 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000000265 homogenisation Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000009749 continuous casting Methods 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 229910018084 Al-Fe Inorganic materials 0.000 description 2
- 229910018192 Al—Fe Inorganic materials 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910001093 Zr alloy Inorganic materials 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 description 2
- 238000004506 ultrasonic cleaning Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IUVCFHHAEHNCFT-INIZCTEOSA-N 2-[(1s)-1-[4-amino-3-(3-fluoro-4-propan-2-yloxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]ethyl]-6-fluoro-3-(3-fluorophenyl)chromen-4-one Chemical compound C1=C(F)C(OC(C)C)=CC=C1C(C1=C(N)N=CN=C11)=NN1[C@@H](C)C1=C(C=2C=C(F)C=CC=2)C(=O)C2=CC(F)=CC=C2O1 IUVCFHHAEHNCFT-INIZCTEOSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910001208 Crucible steel Inorganic materials 0.000 description 1
- 229910019064 Mg-Si Inorganic materials 0.000 description 1
- 229910019752 Mg2Si Inorganic materials 0.000 description 1
- 229910019406 Mg—Si Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- QQHSIRTYSFLSRM-UHFFFAOYSA-N alumanylidynechromium Chemical compound [Al].[Cr] QQHSIRTYSFLSRM-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B21/00—Obtaining aluminium
- C22B21/06—Obtaining aluminium refining
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D1/00—Treatment of fused masses in the ladle or the supply runners before casting
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D21/00—Casting non-ferrous metals or metallic compounds so far as their metallurgical properties are of importance for the casting procedure; Selection of compositions therefor
- B22D21/002—Castings of light metals
- B22D21/007—Castings of light metals with low melting point, e.g. Al 659 degrees C, Mg 650 degrees C
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D43/00—Mechanical cleaning, e.g. skimming of molten metals
- B22D43/001—Retaining slag during pouring molten metal
- B22D43/004—Retaining slag during pouring molten metal by using filtering means
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B21/00—Obtaining aluminium
- C22B21/06—Obtaining aluminium refining
- C22B21/066—Treatment of circulating aluminium, e.g. by filtration
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B9/00—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
- C22B9/02—Refining by liquating, filtering, centrifuging, distilling, or supersonic wave action including acoustic waves
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/02—Making non-ferrous alloys by melting
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
- C22C21/02—Alloys based on aluminium with silicon as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
- C22C21/06—Alloys based on aluminium with magnesium as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
- C22F1/047—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with magnesium as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
- C22F1/05—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys of the Al-Si-Mg type, i.e. containing silicon and magnesium in approximately equal proportions
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
- C22F1/053—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with zinc as the next major constituent
Definitions
- the present invention relates to methods for manufacturing aluminum alloy thick plates, and the resulting aluminum alloy thick plates.
- Aluminum alloy materials such as aluminum alloy thick plates are generally used for various applications including semiconductor-related devices such as base substrates, transport devices, and vacuum chambers; electrical and electronic parts and their manufacturing devices; household articles; and mechanical parts.
- Such aluminum alloy materials are generally manufactured by melting aluminum alloy ingots, and casting the molten material to give a slab, conducting a heat treatment for homogenization, if necessary, and then rolling the slab to a predetermined thickness (see, for example, Paragraphs 0037 to 0045 of Patent Document 1).
- the present invention has been made and an object thereof is to provide a method for manufacturing an aluminum alloy thick plate, which method enables improved accuracy of plate thickness with high productivity and good controllability of surface condition and flatness, and to provide an aluminum alloy thick plate which is manufactured by the procedures of the manufacturing method and excels in surface condition, flatness, and accuracy of plate thickness.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 400°C or higher but lower than its melting point for one hour or longer.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 400°C or higher but lower than its melting point for one hour or longer.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further containing at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0.6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 400°C or higher but lower than its melting point for one hour or longer.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 350°C or higher but lower than its melting point for one hour or longer.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer; and a slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer; and a slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further containing at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0.6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer; and a slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness.
- an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 350°C for one hour or longer; and a slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer.
- an eleventh embodiment of the present invention there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further containing at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0.6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer.
- a method for manufacturing an aluminum alloy thick plate from an aluminum alloy the aluminum alloy containing Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- the method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thickplate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 350°C for one hour or longer.
- an aluminum alloy thick plate which is manufactured by the method for manufacturing an aluminum alloy thick plate, according to any one of the first to twelfth embodiments of the present invention, and includes crystal grains having an average grain size of 400 ⁇ m or less.
- the resulting aluminum alloy thick plate includes finer intermetallic compounds and has improved strength, because the material aluminum alloy has contents of predetermined elements controlled within predetermined ranges.
- the hydrogen gas removal step removes hydrogen to thereby control the concentration of hydrogen in the slab. Therefore, even if crystal grains in the slab become coarse, hydrogen is not accumulated or enriched at the grain boundary near the surface of the slab. This suppresses blistering of the slab and peeling of the aluminum alloy thick plate resulting from the blistering, and also suppresses potential defects on the surface of the thick plates which appear as surface defects of the thick plate.
- the aluminum alloy thick plate has improved strength.
- the filtration step removes inclusions such as oxides and non-metals from the aluminum alloy.
- Slicing the slab in the slicing step reduces the thickness of the oxide film; improves the surface condition, flatness and accuracy of the plate thickness of the aluminum alloy thick plate; and also improves its productivity.
- the heat treatment step thermally treats the aluminum alloy thick plate to thereby remove the internal stress of the aluminum alloy and uniformize its inner structure.
- the aluminum alloy thick plate can have improved strength.
- the aluminum alloy thick plate is manufactured by slicing a slab, and this eliminates necessity to reduce its thickness by hot rolling unlike in known aluminum alloy thick plates. This simplifies operation steps and thereby improves the productivity. This also eliminates unevenness (uneven color) of the surface and cross section of the thick plate; and improves the flatness, surface condition after anodization, and accuracy of plate thickness.
- the internal stress of the aluminum alloy thick plate can be removed and its inner structure can be uniformized.
- the aluminum alloy thick plate can have good flatness and satisfactory accuracy of plate thickness and can maintain its satisfactory strength.
- the configuration (A) helps to further improve the surface condition and flatness of the aluminum alloy thick plate and eliminates the gas accumulation of the surface of the thick plate, because the surface is further smoothened.
- the resulting aluminum alloy thick plate if used as a vacuum chamber, can provide an improved degree of vacuum.
- the configuration (B) helps to provide an aluminum alloy thick plate excellent in appearance quality even after anodization, because the central portion of the slab is removed, which central portion will often cause unevenness in the surface and cross section of the aluminum alloy thick plate after anodization. This configuration also helps to reduce the within-lot variation.
- the aluminum alloy thick plate can include finer intermetallic compounds andhavehigher strength, because the material aluminum alloy has contents of predetermined elements controlled within predetermined ranges.
- the hydrogen gas removal step removes hydrogen gas to thereby control the concentration of hydrogen in the slab. Therefore, even if crystal grains in the slab become coarse, hydrogen is not accumulated or enriched at the grain boundary near the surface of the slab. This suppresses blistering of the slab and peeling of the aluminum alloy thick plate resulting from the blistering; suppresses potential defects on the surface of the thick plates which appear as surface defects of the thick plat; and improves the strength of the aluminum alloy thick plate.
- the filtration step removes inclusions such as oxides and non-metals from the aluminum alloy.
- the heat treatment step thermally treats the slab to eliminate the internal stress and to uniformize the inner structure thereof.
- the slicing step slices the slab so as to reduce the thickness of the oxide film and to improve the surface condition, flatness and accuracy of the plate thickness of the aluminum alloy thick plate, as well as its productivity.
- the aluminum alloy thick plate can have improved balance among its flatness, strength, and cutting property.
- the heat treatment at a temperature of 200°C or higher but lower than 400°C (or 350°C) applied to the slab suppresses the increase in ductility. This helps to remove the internal stress and to uniformize the inner structure of the thick plate without adversely affecting the cutting property (chip breakability).
- the resulting aluminum alloy thick plate can thereby have good flatness and satisfactory accuracy of plate thickness and can maintain its satisfactory strength.
- the aluminum alloy thick plate is manufactured by slicing a slab.
- the configuration (C) helps to further improve the surface condition and flatness of the aluminum alloy thick plate and eliminates the gas accumulation of the surface of the thick plate, because the surface is further smoothened.
- the resulting aluminum alloy thick plate if used as a vacuum chamber, can provide an improved degree of vacuum.
- the configuration (D) helps to provide an aluminum alloy thick plate excellent in appearance quality even after anodization, because the central portion of the slab is removed, which central portion will often cause unevenness in the surface and cross section of the aluminum alloy thick plate after anodization. This configuration also helps to reduce the within-lot variation.
- the aluminum alloy thick plate includes finer intermetallic compounds and has improved strength, because the material aluminum alloy has contents of predetermined elements controlled within predetermined ranges.
- the hydrogen gas removal step removes hydrogen to thereby control the concentration of hydrogen in the slab. Therefore, even if crystal grains in the slab become coarse, hydrogen is not accumulated or enriched at the grain boundary near the surface of the slab. This suppresses blistering of the slab and peeling of the aluminum alloy thick plate resulting from the blistering; suppresses potential defects on the surface of the thick plates which appear as surface defects of the thick plate; and improves the strength of the aluminum alloy thick plate.
- the filtering step removes inclusions such as oxides and non-metals from the aluminum alloy.
- Slicing the slab in the slicing step reduces the thickness of the oxide film; improves the surface condition, flatness and accuracy of the plate thickness of the aluminum alloy thick plate; and improves the productivity of the aluminum alloy thick plate.
- the heat treatment step thermally treats the aluminum alloy thick plate to thereby remove the internal stress of the aluminum alloy and uniformize its inner structure.
- the aluminum alloy thick plate can have improved strength.
- the aluminum alloy thick plate is manufactured by slicing a slab, and this eliminates necessity to reduce its thickness by hot rolling unlike in known aluminum alloy thick plates. This simplifies operation steps; improves the productivity; eliminates unevenness (uneven color) of the surface and cross section of the thick plate; and improves the flatness, quality of appearance after anodization, and accuracy of plate thickness. Further, this also improves the balance among the flatness, strength, and cutting property of the aluminum alloy thick plate.
- the heat treatment at a temperature of 200°C or higher but lower than 400°C (or 350°C) applied to the sliced aluminum alloy thick plate having a predetermined thickness suppresses the increase in ductility, whereby helps to remove the internal stress and uniformize the inner structure of the aluminum alloy thick plate without adversely affecting the cutting property (chip breakability).
- the resulting aluminum alloy thick plate can thereby have good flatness and satisfactory accuracy of plate thickness and maintain its satisfactory strength.
- the configuration (E) helps to further improve the surface condition and flatness of the aluminum alloy thick plate and eliminates the gas accumulation of the surface of the thick plate, because the surface is further smoothened.
- the resulting aluminum alloy thick plate if used as a vacuum chamber, can provide an improved degree of vacuum.
- the configuration (F) helps to provide an aluminum alloy thick plate excellent in appearance quality even after anodization, because the central portion of the slab is removed, which central portion will often cause unevenness in the surface and cross section of the aluminum alloy thick plate after anodization. This configuration also helps to reduce the within-lot variation.
- the aluminum alloy thick plates according to the thirteenth embodiment of the present invention excel in surface condition, flatness, and accuracy of plate thickness. They also have high quality, because their surface is smoothened and thereby is free from gas accumulation. They can be used in a wide variety of applications and can be recycled and used for other applications, because the surface appearance of them after anodization is substantially free from unevenness.
- the methods for manufacturing an aluminum alloy thick plate each include a melting step (S1), a hydrogen gas removal step (S2), a filtration step (S3), a casting step (S4), a slicing step (S5), and a heat treatment step (S6) in this order.
- the methods may further include, where necessary, a surface smoothing treatment step (S7) subsequent to the heat treatment step (S6).
- aluminum alloy ingots are melted in the melting step (S1).
- hydrogen gas is removed from the molten aluminum alloy in the hydrogen gas removal step (S2), and inclusions such as oxides and non-metals are removed therefrom in the filtration step (S3).
- the resulting aluminum alloy is cast into a slab in the casting step (S4).
- the slab is then sliced into an aluminum alloy thick plate having a predetermined thickness in the slicing step (S5).
- the aluminum alloy thick plate having a predetermined thickness is then subjected to a heat treatment in the heat treatment step (S6) and, where necessary, subjected to a surface smoothing treatment in the surface smoothing treatment step (S7).
- the manufacturing methods according to the first, second, third, and fourth embodiments of the present invention use a 5000 series Al-Mg alloy, a 3000 series Al-Mn alloy, a 6000 series Al-Mg-Si alloy, and a 7000 series Al-Zn-Mg alloy, respectively, as a raw material aluminum alloy.
- the details of them are as follows.
- a 5000 series Al-Mg alloy is used.
- the aluminum alloy contains Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further contains at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0. 3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- Magnesium (Mg) serves to improve the strength of the aluminum alloy. Mg, if its content is less than 1.5 percent by mass, may not exhibit the activity sufficiently. In contrast, Mg, if its content is more than 12.0 percent by mass, may significantly adversely affect the casting ability, and this may impede the manufacture of the product. Accordingly, the Mg content should be 1.5 percent by mass or more and 12.0 percent by mass or less.
- Si serves to improve the strength of the aluminum alloy.
- Si is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al- (Fe) - (Mn) -Si intermetallic compound together with Mn and Fe in the slab typically in the casting step (S4).
- Si if its content is more than 0.7 percent by mass, may cause a coarse intermetallic compound in the slab to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Si content should be 0.7 percent by mass or less.
- Fe Iron
- Fe allows crystal grains of the aluminum alloy to be finer and more stabilized and allows the aluminum alloy to have improved strength.
- Fe is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al-Fe- (Mn) - (Si) intermetallic compound together with Mn and/or Si in the slab typically in the casting step (S4).
- Fe if its content is more than 0.8 percent by mass, may cause a coarse intermetallic compound in the slab to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Fe content should be 0.8 percent by mass or less.
- Copper (Cu) serves to improve the strength of the aluminum alloy.
- a Cu content of 0.6 percent by mass is enough to ensure a sufficient strength to be used endurably as a thick plate. Accordingly, the Cu content should be 0.6 percent by mass or less.
- Manganese (Mn) is solidly dissolved in the aluminum alloy and thereby serves to improve the strength of the aluminum alloy. Mn, if its content is more than 1.0 percent by mass, may cause a coarse intermetallic compound to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Mn content should be 1.0 percent by mass or less.
- Chromium (Cr) serves to suppress the grain growth by depositing as a fine compound in the casting step (S4) and heat treatment step (S6).
- Cr if its content is more than 0.5 percent by mass, may cause a coarse Al-Cr intermetallic compound as a primary crystal to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Cr content should be 0.5 percent by mass or less.
- Zinc (Zn) serves to improve the strength of the aluminum alloy.
- a Zn content of 0.4 percent by mass is enough to ensure a sufficient strength to be used endurably as a thick plate. Accordingly, the Zn content should be 0.4 percent by mass or less.
- Titanium (Ti) allows the slab to contain finer crystal grains. If the Ti content is more than 0.1 percent by mass, the activity may be saturated. Accordingly, the Ti content should be 0.1 percent by mass or less.
- Zirconium allows the slab to contain finer crystal grains. If the Zr content is more than 0.3 percent by mass, the activity may be saturated. Accordingly, the Zr content should be 0.3 percent by mass or less.
- the aluminum alloy contains the above-mentioned components, with the remainder being aluminum and inevitable impurities.
- Exemplary inevitable impurities include V and B.
- a 3000 series Al-Mn alloy is used.
- the aluminum alloy contains Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further contains at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- Manganese (Mn) is solidly dissolved in the aluminum alloy and thereby serves to improve the strength of the aluminum alloy. Mn, if its content is less than 0.3 percent by mass, maynot exhibit the activity sufficiently. In contrast, Mn, if its content is more than 1.6 percent by mass, may cause a coarse intermetallic compound, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Mn content should be 0.3 percent by mass or more and 1.6 percent by mass or less.
- Magnesium (Mg) serves to improve the strength of the aluminum alloy.
- aMg content of 1. 5percentbymass is enough to ensure a sufficient strength to be used endurably as a thick plate. Accordingly, the Mg content should be 1.5 percent by mass or less.
- a 6000 series Al-Mg-Si alloy is used.
- the aluminum alloy contains Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further contains at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0.6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- Si serves to improve the strength of the aluminum alloy.
- Si is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al-(Fe)-Si intermetallic compound and a Si intermetallic compound in the slab typically in the casting step (S4).
- Si if its content is less than 0.2 percent by mass, may not exhibit the activity sufficiently. In contrast, Si, if its content is more than 1.6 percent by mass, may cause a coarse Si intermetallic compound in the slab, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Si content should be 0.2 percent by mass or more and 1.6 percent by mass or less.
- Mg Magnesium (Mg) forms Mg 2 Si in the coexistence with Si to thereby serve to improve the strength of the aluminum alloy. Mg, if its content is less than 0.3 percent by mass, may not exhibit the activity sufficiently. In contrast, if the Mg content is more than 1.5 percent by mass, the activity may be saturated. Accordingly, the Mg content should be 0.3 percent by mass or more and 1.5 percent by mass or less.
- Copper (Cu) serves to improve the strength of the aluminum alloy.
- Cu if its content is more than 1.0 percent by mass, may impair the corrosion resistance. Accordingly, the Cu content should be 1.0 percent by mass or less.
- Zn serves to improve the strength of the aluminum alloy. Zn, if its content is more than 0.4 percent by mass, may impair the corrosion resistance. Accordingly, the Zn content should be 0.4 percent by mass or less.
- a 7000 series Al-Zn-Mg alloy is used.
- the aluminum alloy contains Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9.0 percent by mass or less, and further contains at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- Magnesium (Mg) serves to improve the strength of the aluminum alloy. Mg, if its content is less than 0.4 percent by mass, may not exhibit the activity sufficiently. In contrast, Mg, if its content is more than 4.0 percent by mass, may often cause unevenness in the surface appearance after anodization. Accordingly, the Mg content should be 0.4 percent by mass or more and 4.0 percent by mass or less.
- Zinc (Zn) serves to improve the strength of the aluminum alloy. Zn, if its content is less than 3.0 percent by mass, may not exhibit the activity sufficiently. In contrast, Zn, if its content is more than 9. 0 percent by mass, may often cause unevenness in the surface appearance after anodization. Accordingly, the Zn content should be 3.0 percent by mass or more and 9.0 percent by mass or less.
- Silicon (Si) is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al-(Fe)-Si intermetallic compound in the slab typically in the casting step (S4).
- Si if its content is more than 0.7 percent by mass, may cause a coarse Al- (Fe) -Si intermetallic compound in the slab, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Si content should be 0.7 percent by mass or less.
- Iron (Fe) is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al-Fe intermetallic compound in the slab typically in the casting step (S4).
- Fe if its content is more than 0.8 percent by mass, may cause a coarse Al-Fe intermetallic compound in the slab, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Fe content should be 0.8 percent by mass or less.
- Copper (Cu) serves to improve the strength of the aluminum alloy.
- Cu if its content is more than 3.0 percent by mass, may impair the corrosion resistance. Accordingly, the Cu content should be 3.0 percent by mass or less.
- Manganese (Mn) allows the crystal structure to be finer. Mn, if its content is more than 0.8 percent by mass, may cause a coarse intermetallic compound, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Mn content should be 0.8 percent by mass or less.
- the melting step (S1) is a step of melting the raw material aluminum alloy.
- the hydrogen gas removal step (S2) is a step of removing hydrogen gas from the aluminum alloy which has been melted in the melting step (S1).
- Hydrogen gas is generated typically from hydrogen in a fuel and from water and organic substances attached typically to the ingot. Hydrogen gas, if contained in a large content, will cause the following disadvantages.
- the amount of hydrogen gas is preferably 0.2 ml or less and more preferably 0.1 ml or less per 100 g of the aluminum alloy.
- Removal of hydrogen gas can be suitably carried out by subjecting a moltenmetal typically to a fluxing process, chlorine refining, or in-line refining, and it can be more suitably carried out by using a SNIF (spinning nozzle inert flotation) system and a porous plug (see JP-ANo. 2002-146447 ) in a hydrogen gas removing apparatus.
- SNIF spininning nozzle inert flotation
- the concentration of hydrogen gas in a slab can be determined typically in the following manner. Specifically, a sample is cut out from the slab after the casting step; then subj ected to ultrasonic cleaning with alcohol and acetone; and thereafter analyzed typically according to the inert gas fusion thermal conductivity method (LIS A06-1993).
- the concentration of hydrogen gas in an aluminum alloy thick plate can be determined typically in the following manner. Specifically, a sample is cut out from the aluminum alloy thick plate. Next, the sample is immersed in an aqueous NaOH solution; then treated with nitric acid to remove an oxide film on the surface of the sample; and the treated sample is subjected to ultrasonic cleaning with alcohol and acetone and then analyzed according typically to the vacuum heat extraction capacitance method (LIS A06-1993).
- the filtration step (S3) is a step of removing mainly oxide and non-metal inclusions from the aluminum alloy with a filtrating device.
- the filtrating device is provided typically with a ceramic tube with alumina particles of about 1 mm. The inclusions are removed by allowing a molten metal to pass through the ceramic tube.
- the hydrogen gas removal step and the filtration step ensure high quality of the aluminum alloy, and the resulting aluminum alloy is made into a high-quality slab in the subsequent casting step (S4). These steps can suppress the generation of deposits of oxides (dross), and this reduces the effort and time for removing the dross.
- the casting step (S4) is a step of producing a slab by forming a molten metal of the aluminum alloy typically with a casting apparatus into a predetermined shape such as a rectangular parallelepiped and solidifying the metal.
- a casting apparatus equipped with a water-cooled mold is used.
- a semi-continuous casting process may be employed as the casting process.
- a molten metal of the aluminum alloy is injected from above into a water-cooled metallic mold having an open bottom, and the solidified aluminum alloy is successively withdrawn from the bottom of the water-cooled mold to give slabs having predetermined thickness.
- the semi-continuous casting process may be carried out vertically or horizontally.
- the slicing step (S5) is a step of producing an aluminum alloy thick plate having a predetermined thickness by slicing the slab produced in the casting step (S4).
- the slab slicing process may be employed as a slicing process.
- the slab slicing process is a process for cutting out the slab in the cast direction by slicing the slab produced by the semi-continuous casting process typically with a band saw cutting apparatus, to give an aluminum alloy thick plate having a predetermined thickness.
- the thickness of the aluminum alloy thick plate is preferably 15 to 200 mm, but it is not particularly limited, and can be varied suitably depending on the intended use of the aluminum alloy thick plate.
- a band saw is preferably used in the slicing process, but it is not particularly limited, and cutting may be also performed typically with a circular saw cutting apparatus, or by laser or water pressure.
- Slicing the slab gives an aluminum alloy thick plate superior typically in surface condition, flatness, and accuracy of the plate thickness to a rolled product.
- a thick plate having a flatness (amount of warpage) per 1 m in the casting direction of 0.4 mm or less per 1 m length in the evaluation of flatness, and the accuracy of the plate thickness of ⁇ 100 ⁇ m or less.
- a central portion B shaded with slanted lines is preferably removed in the slicing step (S5).
- the central portion B has two substantially identical thicknesses in a thickness direction from the center of the thickness direction A to the both surfaces of the central portion, respectively, and has a total thickness of from one-thirtieth to one-fifth the thickness T of the slab 1 (T/30 to T/5).
- the central portion B in Fig. 2 is illustrated to have a thickness about one-fifth the thickness T.
- the thicknesses b1 and b2 of the upper and lower portions of the central portion B of the slab 1 are preferably equal to each other, but a difference between them of about 30% is acceptable.
- the center of the thickness direction A refers to a location which is the center of the slab 1 in the thickness direction and is located about a half the thickness T of the slab 1, i.e., a location of the slab 1 about T/2 deep.
- the central portion B of the slab 1 is susceptive to unevenness in the surface and cross section of the thick plate after anodization.
- the central portion B is removed by the slicing step (S5), and a thick plate excellent in quality of appearance after anodization with less within-lot variation can be obtained.
- Removal of a central portion having a thickness of less than T/30 (one-thirtieth the thickness T) may often cause a thick plate suffering from unevenness in the surface appearance after anodization and often cause a large within-lot variation.
- T/5 one-fifth the thickness T
- the central portion B of the slab 1 is preferably removed in such an amount that the central portion has two substantially identical thicknesses in the thickness direction from the center of the thickness direction A to the both surfaces of the central portion, respectively, and has a total thickness of from one-thirtieth to one-fifth the thickness T of the slab 1 (T/30 to T/5).
- the subsequent heat treatment step (S6) is performed in which a heat treatment is conducted in order to remove the internal stress and to uniformize the inner structure.
- the heat treatment improves the flatness, accuracy of plate thickness, and quality of appearance after anodization.
- the heat treatment step (S6) is a step of carrying out a heat treatment (heat treatment for homogenization) on the aluminum alloy thick plate having a predetermined thickness produced in the slicing step (S5).
- the heat treatment may be carried out according to a common procedure. Specifically, when the aluminum alloy is a 5000 series Al-Mg alloy (the first embodiment of the present invention), a 3000 series Al-Mn alloy (the second embodiment of the present invention), and a 6000 series Al-Mg-Si alloy (the third embodiment of the present invention), the heat treatment is performed by holding the aluminum alloy thick plate at a temperature of 400°C or higher but lower than its melting point for one hour or longer. When the aluminum alloy is a 7000 series Al-Zn-Mg alloy (the fourth embodiment of the present invention), the heat treatment is performed by holding the aluminum alloy thick plate at a temperature of 350°C or higher but lower than its melting point for one hour or longer.
- the slicing process of the slab obtained in the casting step (S4) allows the internal residual stress to be released, and this often causes warpage.
- a heat treatment if conducted at a temperature of lower than 400°C, may not sufficiently help to remove the inner stress and to uniformize a solute element, which is segregated during casting, and the heat treatment may therefore not exhibit sufficient advantages.
- the treatment temperature herein should be 400°C or higher. If a heat treatment is conducted at a temperature equal to or higher than the melting point, part of the surface of the slab is melted, to cause an internal defect and to impair the strength/ductility. Accordingly, the treatment temperature should be lower than the melting point.
- a heat treatment if conducted at a temperature of lower than 350°C, may not sufficiently help to remove the inner stress and to uniformize a solute element, which is segregated during casting, and therefore may exhibit less advantages. Accordingly, the treatment temperature herein should be 350°C or higher. If a heat treatment is conducted at a temperature equal to or higher than the melting point, part of the surface of the slab ismelted, to cause an internal defect and to impair the strength/ductility. Accordingly, the treatment temperature should be lower than the melting point.
- a heat treatment if conducted for a time shorter than one hour, may not sufficiently help intermetallic compounds to be solidly dissolved, and this may often cause the intermetallic compounds to be deposited. Accordingly, the treatment time should be one hour or longer. In contrast, a heat treatment, if conducted for a time of longer than about 8 hours, may be saturated in its effect, and this may cause energy loss. Accordingly, the treatment time is preferably controlled to be 8 hours or shorter.
- the aluminum alloy thick plate after the heat treatment in the heat treatment step (S6) may be subjected to a surface smoothing treatment according to necessity in order to remove crystallized substances and oxides generated on the surface of the thick plate or to eliminate gas accumulation in the surface of the thick plate.
- the surface smoothing treatment step (S7) is a step of subjecting the surface of the aluminum alloy thick plate produced in the heat treatment step (S6) to a surface smoothing treatment.
- exemplary surface smoothing treatments include, but are not limited to, cutting such as end mill cutting and diamond bite cutting; grinding which faces the surface typically with a grindstone; and polishing such as buff polishing.
- a vacuum chamber suffers from a decrease in the degree of vacuum therein caused by, when the chamber is decompressed to attain high vacuum, releasing of adsorbed gas from the inner surface of the chamber and releasing of gas atoms which are solidly dissolved in the thick plate onto the surface. This elongates the time which takes to reach a target degree of vacuum and thereby lowers production efficiency.
- the following conditions are required for the aluminum alloy thick plate used for a chamber: the amount of gas which adsorbs onto the surface of the thick plate positioned in an inner portion of the chamber is low; and the gas atoms which are solidly dissolved in the thick plate are not released even in high vacuum.
- the surface smoothing treatment herein satisfies these conditions.
- the methods for manufacturing an aluminum alloy thick plate each include a melting step (S1), a hydrogen gas removal step (S2), a filtration step (S3), a casting step (S4), a heat treatment step (S5), and a slicing step (S6) in this order.
- the methods may further include, where necessary, a surface smoothing treatment step (S7) subsequent to the slicing step (S6).
- a raw material aluminum alloy is melted in the melting step (S1).
- hydrogen gas is removed from the molten aluminum alloy in the hydrogen gas removal step (S2), and inclusions such as oxides and non-metals are removed therefrom in the filtration step (S3).
- the resulting aluminum alloy is cast into a slab in the casting step (S4).
- the slab is subjected to a heat treatment in the heat treatment step (S5) and is then sliced into an aluminum alloy thick plate having a predetermined thickness in the slicing step (S6).
- the aluminum alloy thick plate having a predetermined thickness is further subjected to a surface smoothing treatment in the surface smoothing treatment step (S7).
- the manufacturing methods according to the fifth, sixth, seventh, and eighth embodiments of the present invention use, as a raw material aluminum alloy, a 5000 series Al-Mg alloy, a 3000 series Al-Mn alloy, a 6000 series Al-Mg-Si alloy, and a 7000 series Al-Zn-Mg alloy, respectively.
- the details of them are as follows.
- a 5000 series Al-Mg alloy as in the first embodiment of the present invention is used in this embodiment.
- the composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the first embodiment of the present invention.
- a 3000 series Al-Mn alloy as in the second embodiment of the present invention is used in this embodiment.
- the composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the second embodiment of the present invention.
- a 6000 series Al-Mg-Si alloy as in the third embodiment of the present invention is used in this embodiment.
- the composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the third embodiment of the present invention.
- a 7000 series Al-Zn-Mg alloy as in the fourth embodiment of the present invention is used in this embodiment.
- the composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the fourth embodiment of the present invention.
- This step is the same as with the melting step (S1) in the first to fourth embodiments of the present invention.
- This step is the same as with the hydrogen gas removal step (S2) in the first to fourth embodiments of the present invention.
- This step is the same as with the filtration step (S3) in the first to fourth embodiments of the present invention.
- This step is the same as with the casting step (S4) in the first to fourth embodiments of the present invention.
- a heat treatment is carried out in the subsequent heat treatment step (S5), for the purpose of removing internal stress and uniformizing the inner structure.
- the heat treatment of the slab helps to improve the flatness, accuracy of plate thickness, and quality of appearance after anodization.
- the heat treatment step (S5) is a step of subj ecting the slab produced in the casting step (S4) to a heat treatment (heat treatment for homogenization).
- the heat treatment is carried out according to a common procedure. Specifically, when the aluminum alloy is a 5000 series Al-Mg alloy (the fifth embodiment of the present invention), a 3000 series Al-Mn alloy (the sixth embodiment of the present invention), and a 6000 series Al-Mg-Si alloy (the seventh embodiment of the present invention), the heat treatment is performed by holding the slab at a temperature of 200°C or higher but lower than 400°C for one hour or longer. When the aluminum alloy is a 7000 series Al-Zn-Mg alloy (the eighth embodiment of the present invention), the heat treatment is performed by holding the slab at a temperature of 200°C or higher but lower than 350°C for one hour or longer.
- a heat treatment if conducted at a temperature of lower than 200°C, may not sufficiently help to remove the inner stress and therefore may not exhibit satisfactory advantages. Accordingly, the treatment temperature should be 200°C or higher. In contrast, a heat treatment, if conducted at a temperature of 400°C or higher, may excessively increase the ductility and lower the strength and cutting property.
- cutting property refers to chip breakability. Chips (scraps) are preferably formed as small or short pieces. This is because long chips become entangled with a working tool (blade) and are rotated therewith, and this damages the surface of the thick plate and breaks the tool. Accordingly, the treatment temperature should be lower than 400°C. A heat treatment performed under above-specified temperature conditions helps to improve the flatness and accuracy of plate thickness without adversely affecting the strength and cutting property.
- a heat treatment if performed at a temperature of lower than 200°C, may not sufficiently help to remove the inner stress and therefore may not exhibit satisfactory advantages. Accordingly, the treatment temperature should be 200°C or higher. In contrast, a heat treatment, if conducted at a temperature of 350°C or higher, may excessively increase the ductility and lower the strength and cutting property.
- cutting property refers to chip breakability. Chips (scraps) are preferably formed as small or short pieces. This is because long chips become entangled with a working tool (blade) and are rotated therewith, and this damages the surface of the thick plate and breaks the tool. Accordingly, the treatment temperature should be lower than 350°C. A heat treatment performed under above-specified temperature conditions helps to improve the flatness and accuracy of plate thickness without adversely affecting the strength and cutting property.
- a heat treatment if conducted for a time shorter than one hour, may not sufficiently help intermetallic compounds to be solidly dissolved, and this may often cause the intermetallic compounds to be deposited. Accordingly, the treatment time shouldbe one hour or longer.
- a heat treatment if conducted for a time of longer than about 8 hours, may be saturated in its effect, and this may cause energy loss. Accordingly, the treatment time is preferably controlled to be 8 hours or shorter.
- the slicing step (S6) is a step of slicing the slab obtained in the heat treatment step (S5) into an aluminum alloy thick plate having a predetermined thickness.
- the details of this step are as with the slicing step (S5) in the first to fourth embodiments of the present invention.
- the aluminum alloy thick plate produced in the slicing step (S6) may be subjected to a surface smoothing treatment according to necessity in order to remove crystallized substances and oxides formed on the surface of the thick plate or to eliminate gas accumulation in the surface of the thick plate.
- the surface smoothing treatment step (S7) is a step of subjecting the surface of the aluminum alloy thick plate produced in the slicing step (S6) to a surface smoothing treatment.
- the details of this step are as with the surface smoothing treatment step (S7) in the first to fourth embodiments of the present invention.
- the methods for manufacturing an aluminum alloy thick plate each include a melting step (S1), a hydrogen gas removal step (S2), a filtration step (S3), a casting step (S4), a slicing step (S5), and a heat treatment step (S6) in this order.
- the methods may further include, where necessary, a surface smoothing treatment step (S7) subsequent to the heat treatment step (S6).
- a raw material aluminum alloy is melted in the melting step (S1).
- hydrogen gas is removed from the molten aluminum alloy in the hydrogen gas removal step (S2), and inclusions such as oxides and non-metals are removed therefrom in the filtration step (S3).
- the resulting aluminum alloy is cast into a slab in the casting step (S4).
- the slab is then sliced into an aluminum alloy thick plate having a predetermined thickness in the slicing step (S5).
- the aluminum alloy thick plate having a predetermined thickness is then subjected to a heat treatment in the heat treatment step (S6) and, where necessary, further subjected to a surface smoothing treatment in the surface smoothing treatment step (S7).
- the manufacturing methods according to the ninth, tenth, eleventh, and twelfth embodiments of the present invention use a 5000 series Al-Mg alloy, a 3000 series Al-Mn alloy, a 6000 series Al-Mg-Si alloy, and a 7000 series Al-Zn-Mg alloy, respectively, as a raw material aluminum alloy.
- the details of them are as follows.
- a 5000 series Al-Mg alloy as in the first embodiment of the present invention is used in this embodiment.
- the composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the first embodiment of the present invention.
- a 3000 series Al-Mn alloy as in the second embodiment of the present invention is used in this embodiment.
- the composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the second embodiment of the present invention.
- a 6000 series Al-Mg-Si alloy as in the third embodiment of the present invention is used in this embodiment.
- the composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the third embodiment of the present invention.
- a 7000 series Al-Zn-Mg alloy as in the fourth embodiment of the present invention is used in this embodiment.
- the composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the fourth embodiment of the present invention.
- This step is the same as with the melting step (S1) in the first to fourth embodiments of the present invention.
- This step is the same as with the hydrogen gas removal step (S2) in the first to fourth embodiments of the present invention.
- This step is the same as with the filtration step (S3) in the first to fourth embodiments of the present invention.
- This step is the same as with the casting step (S4) in the first to fourth embodiments of the present invention.
- This step is the same as with the slicing step (S5) in the first to fourth embodiments of the present invention.
- the heat treatment step (S6) is a step of carrying out a heat treatment (heat treatment for homogenization) on the aluminum alloy thick plate having a predetermined thickness produced in the slicing step (S5).
- the heat treatment may be carried out according to a common procedure. Specifically, when the aluminum alloy is a 5000 series Al-Mg alloy (the ninth embodiment of the present invention), a 3000 series Al-Mn alloy (the tenth embodiment of the present invention), anda 6000 seriesAl-Mg-Si alloy (the eleventh embodiment of the present invention), the heat treatment is performed by holding the aluminum alloy thick plate at a temperature of 200°C or higher but lower than 400°C for one hour or longer.
- the heat treatment is performed by holding the aluminum alloy thick plate at a temperature of 200°C or higher but lower than 350°C for one hour or longer.
- the details of the other conditions and procedures are as with the heat treatment step (S6) in the first to fourth embodiments of the present invention.
- a heat treatment if conducted at a temperature of lower than 200°C may not sufficiently help to remove the inner stress and therefore may not exhibit satisfactory advantages. Accordingly, the treatment temperature should be 200°C or higher. In contrast, a heat treatment, if conducted at a temperature of 400°C or higher, may excessively increase the ductility and lower the strength and cutting property.
- cutting property refers to chip breakability. Chips (scraps) are preferably formed as small or short pieces. This is because long chips become entangled with a working tool (blade) and are rotated therewith, and this damages the surface of the thick plate and breaks the tool. Accordingly, the treatment temperature should be lower than 400°C. A heat treatment performed under above-specified temperature conditions helps to improve the flatness and accuracy of plate thickness without adversely affecting the strength and cutting property.
- a heat treatment if conducted at a temperature of lower than 200°C, may not sufficiently help to remove the inner stress and therefore may not exhibit satisfactory advantages. Accordingly, the treatment temperature should be 200°C or higher. In contrast, a heat treatment, if conducted at a temperature of 350°C or higher, may excessively increase the ductility and lower the strength and cutting property.
- cutting property refers to chip breakability. Chips (scraps) are preferably formed as small or short pieces. This is because long chips become entangled with a working tool (blade) and are rotated therewith, and this damages the surface of the thick plate and breaks the tool. Accordingly, the treatment temperature should be lower than 350°C. A heat treatment performed under above-specified temperature conditions helps to improve the flatness and accuracy of plate thickness without adversely affecting the strength and cutting property.
- a heat treatment if conducted for a time shorter than one hour, may not sufficiently help intermetallic compounds to be solidly dissolved, and this may often cause the intermetallic compounds to be deposited. Accordingly, the treatment time shouldbe one hour or longer.
- a heat treatment if conducted for a time of longer than about 8 hours, may be saturated in its effect, and this may cause energy loss. Accordingly, the treatment time is preferably controlled to be 8 hours or shorter.
- This step is the same as with the surface smoothing treatment step (S7) in the first to fourth embodiments of the present invention.
- These aluminum alloy thick plates are manufactured by the procedures of the manufacturing method according to any one of the first to twelfth embodiments of the present invention and have an average crystal grain size of 400 ⁇ m or less.
- the aluminum alloy thick plates according to the present invention have an average crystal grain size of 400 ⁇ m or less whereby can have improved quality of appearance after anodization and show a smaller within-lot variation.
- a thick plate if containing intermetallic compounds having large sizes, suffers from unevenness (uneven color) of the cross section and surface of the thick plate upon anodization.
- the aluminum alloy thick plates according to the present invention contain intermetallic compounds with small sizes and are thereby resistant to such unevenness.
- the measurement of the crystal grain size may be carried out, for example, in the following manner. Specifically, measurements are conducted in cross sections at four points, i.e., at thicknesses of T/5, 2T/5, 3T/5, and 4T/5 ranging from one surface of the slab to the other, wherein T represents the thickness of the slab, and the four measured data are averaged. These measured data are determined typically according to a cutting method. In the cutting method, cross sections of the aluminum alloy thick plate are etched according to a Barker method and are observed with an optical microscope.
- the control of the average crystal grain size to 400 ⁇ m or less may be carried out typically in the following manner. Specifically, a cooling rate (average cooling rate from the liquidus temperature to the solidus temperature) during casting is set to be 0.2°C/second or more. Additionally, the aluminum alloy contains 0.1 percent by mass or less of Ti or 0. 3 percent by mass or less of Zr and thereby the crystal grain size can be more finer (smaller) in the manufacturing methods according to the first to third embodiments, the fifth to seventh embodiments, and the ninth to eleventh embodiments of the present invention.
- the aluminum alloy contains 0.1 percent by mass or less of Ti or 0.25 percent by mass or less of Zr and thereby the crystal grain size can be more finer (smaller) in the manufacturing methods according to the fourth, eighth, and twelfth embodiments of the present invention.
- the resulting aluminum alloy thick plates manufactured by the procedures of the manufacturing methods according to the first to twelfth embodiments of the present invention are satisfactory in the surface condition, flatness, and accuracy of plate thickness as described above and can be used for various applications including semiconductor-related devices such as base substrates, transport devices, and vacuum chambers; electrical and electronic parts and their manufacturing devices; household articles; and mechanical parts. Additionally, they can be recycled and used for other applications.
- This experimental example relates to the first embodiment of the present invention.
- the experimental example used 5000 series Al-Mg alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 1A to 22A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- sliced samples and hot-rolled samples were prepared from the slabs.
- the sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 500°C for 4 hours
- the resulting sliced samples are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the first embodiment of the present invention, but the resulting hot-rolled samples are not.
- the sliced samples using Alloys 1A to 22A correspond to examples according to the first embodiment of the present invention.
- the sliced samples were tested to determine their amounts of warpage (flatness) per 1 m in the casting direction, while the hot-rolled samples were tested to determine their amounts of warpage (flatness) per 1 m in the rolling direction.
- Samples having an amount of warpage of 0.4 mm or less per 1 m length were evaluated as having accepted flatness (Accepted), while those having an amount of warpage of more than 0.4 mm per 1 m length were evaluated as having unaccepted flatness (Failed).
- thicknesses at six positions of each sample were measured with a micrometer.
- the six positions are the four corners of the sample thickplate, and two positions each located at a half the length of the long sides and 20 mm inside in the width direction of the thick plate.
- Samples having thicknesses of 19.94 mm or more and 20.06 mm or less at all the six positions were evaluated as having excellent accuracy of plate thickness (Excellent); and those having thicknesses of 19.90 mm or more and 20.10 mm or less at all the six positions were evaluated as having accepted accuracy of plate thickness (Accepted).
- the strength test was conducted in the following manner. Specifically, JIS No. 5 test pieces were prepared from the aluminum alloy thick plates to perform tensile test thereon, and their tensile strength and 0.2%-proof stress were measured. Samples having a tensile strength of 180 N/mm 2 or more were evaluated as having accepted strength (Accepted) ; while those having a tensile strength of less than 180 N/mm 2 were evaluated as having unaccepted strength (Failed).
- the anodiz ability evaluation was carried out in the following manner. Anodized aluminum films having a thickness of 10 ⁇ m were formed on surface and cross sections of the aluminum alloy thick plates by sulfuric acid anodization under conditions of 15% sulfuric acid, 20°C, and a current density of 2 A/dm 2 . The appearances of surfaces and cross sections of the thick plates were observed. Samples showing no unevenness (uneven color) in their appearances were evaluated as having accepted anodizability (Accepted); while those showing unevenness in their appearances were evaluated as having unaccepted anodizability (Failed).
- the average crystal grain sizes of the thick plates were determined.
- the measurements of the average crystal grain sizes were carried out in the following manner. Specifically, measurements were conducted in cross sections at four points, i.e., at thicknesses of T/5, 2T/5, 3T/5, and 4T/5 ranging from one surface of the slab to the other, wherein T represents the thickness of the slab, and the four measured data were averaged. These measured data were determined according to the cutting method. In the cutting method, cross sections of the aluminum alloy thick plate were etched according to the Barker method and were observed with an optical microscope.
- Table 2 shows the test results of the sliced samples, in which Alloys 1A to 12A correspond to Examples, and Alloys 13A to 22A correspond to comparative examples.
- Table 3 shows the test results of the hot-rolled samples, in which all Alloys 1A to 22A correspond to comparative examples.
- the samples using Alloys 1A to 13A and 15A to 22A had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
- the sample using Alloy 14A contained Mg in a content of more than its upper limit in the material aluminum alloy, thereby suffered from casting cracks, and was unproducible.
- the sample using Alloy 13A contained Mg in a content of less than its lower limit in the material aluminum alloy and thereby had insufficient strength.
- the samples using Alloys 1A to 13A, 17A, and 20A to 22A did not suffer fromunevenness in their appearances of surfaces after anodization.
- the samples using Alloys 15A, 16A, 18A, and 19A contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, thereby caused a coarse intermetallic compound, and suffered from unevenness in their appearances of surfaces after anodization.
- the samples using Alloys 1A to 13A and 15A to 22A did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 17A, 20A, 21A, and 22A contained Cu, Zn, Ti, and Zr, respectively, in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were thereby saturated, resulting in inferior economical efficiency.
- the samples using Alloys 1A to 13A and 15A to 22A had accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them showed somewhat inferior accuracy of plate thickness to the sliced samples.
- the sample using Alloy 14A contained Mg in a content of more than the upper limit in the material aluminum alloy, suffered from casting cracks, and was unproducible.
- the sample using Alloy 13A contained Mg in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the samples using Alloys 15A, 16A, 18A, and 19A contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization.
- This experimental example relates to the first embodiment of the present invention.
- the experimental example used Alloy 3A in Table 1.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloy 3A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- the slabs were further subjected to a slicing step to give sliced samples.
- the sliced samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were then subjected to a heat treatment step. Specifically, the sliced samples were further subjected to a heat treatment under conditions given in Table 4.
- Samples A1 and A2, whose heat treatment conditions satisfy the conditions according to the first embodiment of the present invention, correspond to examples according to the first embodiment of the present invention; whereas Samples A3 to A5, whose heat treatment conditions do not satisfy the conditions according to the first embodiment of the present invention, correspond to comparative examples.
- the evaluation test for accuracy of plate thickness is as in First Experimental Example.
- ExamplesAl andA2 whoseheat treatment conditions satisfy the conditions specified in the first embodiment of the present invention, excelled in flatness and accuracy of plate thickness.
- Comparative Example A3 did not undergo a heat treatment and was thereby somewhat inferior in flatness and accuracy of plate thickness to Examples A1 and A2.
- Comparative Example A4 underwent a heat treatment at a temperature lower than the temperature range specified in the first embodiment of the present invention (lower than 400°C) and was thereby somewhat inferior in flatness to Examples A1 andA2.
- Comparative Example A5 underwent a heat treatment at a temperature higher than the temperature range specified in the first embodiment of the present invention (higher than the melting point), whereby suffered from internal partial melting and resulting internal defects, and was unproducible.
- This experimental example relates to the second embodiment of the present invention.
- the experimental example used 3000 series Al-Mn alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 23A to 26A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- sliced samples and hot-rolled samples were prepared from the slabs.
- the sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 500°C for 4 hours.
- the sliced samples after the treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the second embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 23A and 24A correspond to examples according to the second embodiment of the present invention.
- the prepared sliced samples and hot-rolled samples were further subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, a strength test, and an anodizability evaluation test.
- the samples using Alloys 23A to 26A had small processing strain and showed little warpage, i.e., they had satisfactoryflatness. Additionally, theyexcelledin accuracy of plate thickness.
- the sample using Alloy 25A contained Mn in a content less than the lower limit in the material aluminum alloy and thereby had insufficient strength.
- the sample using Alloy 26A contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization.
- the samples using Alloys 23A to 26A did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloy 23A to 26A suffered from accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them were somewhat inferior in accuracy of plate thickness to the corresponding sliced samples.
- the sample using Alloy 25A contained Mn in a content of less than the lower limit in the material aluminum alloy and was thereby somewhat inferior in strength to the other hot-rolled samples.
- the sample using Alloy 26A contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization.
- the samples using Alloy 23A to 26A suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the third embodiment of the present invention.
- the experimental example used 6000 series Al-Mg-Si alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloy 27A to 32A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- sliced samples and hot-rolled samples were prepared from the slabs.
- the sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 500°C for 4 hours.
- the resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 520°C and subsequently to an aging treatment at 175°C for 8 hours.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the third embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 27A and 28A correspond to examples according to the third embodiment of the present invention.
- the samples using Alloys 29A and 31A contained Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the sample using Alloy 30A contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization.
- the sample using Alloy 32A contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency.
- the samples using Alloys 27A to 32A did not suffer fromunevenness in their appearances of cross sections after anodization.
- the samples using Alloys 29A and 31A contained Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the sample using Alloy 30A contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization.
- the sample using Alloy 32A contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency.
- the samples using Alloy 27A to 32A suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the fourth embodiment of the present invention.
- the experimental example used 7000 series Al-Zn-Mg alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 33A to 38A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- sliced samples and hot-rolled samples were prepared from the slabs.
- the sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 500°C for 4 hours.
- the resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 470°C and subsequently to an aging treatment at 120°C for 48 hours.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the fourth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 33A and 34A correspond to examples according to the fourth embodiment of the present invention.
- the samples using Alloys 35A and 37A contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the samples using Alloys 36A and 38A contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and suffered from unevenness in their appearances of surfaces after anodization.
- the samples using Alloys 33A to 38A did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 35A and 37A contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the samples using Alloys 36A and 38A contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and suffered from unevenness in their appearances of surfaces after anodization.
- the samples using Alloys 33A to 38A suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the fifth embodiment of the present invention.
- the experimental example used 5000 series Al-Mg alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 1B to 22B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- the slabs were further subjected to a treatment in a heat treatment step, in which they were held at a temperature of 350°C for 4 hours.
- sliced samples and hot-rolled samples were prepared from the thermally treated slabs.
- the sliced samples were prepared by slicing the slabs in a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the fifth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 1B to 22B correspond to examples according to the fifth embodiment of the present invention.
- Table 12 shows the test results of the sliced samples.
- the samples using Alloys 1B to 12B correspond to examples according to the fifth embodiment of the present invention, whereas the samples using Alloys 13B to 22B correspond to comparative examples.
- Table 13 shows the test results of the hot-rolled samples. In Table 13, all the samples using Alloys 1B to 22B correspond to comparative examples.
- the samples using Alloys 1B to 13B and 15B to 22B had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
- the sample using Alloy 14B contained Mg in a content of more than the upper limit in the material aluminum alloy, thereby suffered from casting cracks, and was unproducible.
- the sample using Alloy 13B contained Mg in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the samples using Alloys 1B to 13B, 17B, and 20B to 22B did not suffer from unevenness in their appearances of surfaces after anodization.
- the samples using Alloys 15B, 16B, 18B, and 19B contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization.
- the samples using Alloys 1B to 13B and 15B to 22B did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 17B, 20B, 21B, and 22B contained Cu, Zn, Ti, and Zr, respectively, in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency.
- the samples using Alloys 15B, 16B, 18B, and 19B contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization.
- This experimental example relates to the fifth embodiment of the present invention.
- the experimental example used Alloy 3B in Table 11.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloy 3B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- the slabs were further subjected to a treatment in a heat treatment step, in which they were further subjected to a heat treatment under conditions given in Table 14.
- the thermally treated slabs were sliced in a slicing step to give sliced samples.
- the sliced samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- Samples B1 and B2, whose heat treatment conditions satisfy the conditions specified in the fifth embodiment of the present invention, correspond to examples according to the fifth embodiment of the present invention; whereas Samples B3 to B5, whose heat treatment conditions do not satisfy the conditions specified in the fifth embodiment of the present invention, correspond to comparative examples.
- the sliced samples after the treatments were subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, and a cutting property evaluation test.
- the evaluation test for accuracy of plate thickness is as in First Experimental Example.
- the evaluation of cutting property i.e., chip breakability was performed by drilling a sample and measuring the number of chips per unit mass. Specifically, the sample was drilled with a drill having a diameter of 5 mm at a number of revolutions of 7000 rpm and a feed rate of 300 mm/minute, and the number of generated chips per 10 g was measured. Samples having a number of chips of 1000 or more per 10 g were evaluated as having accepted cutting property (Accepted) ; whereas those having a number of chips of less than 1000 per 10 g were evaluated as having unaccepted cutting property (Failed).
- Examples B1 and B2 whose heat treatment conditions satisfy the conditions specified in the fifth embodiment of the present invention, excelled in flatness, accuracy of plate thickness, and cutting property.
- Comparative Example B3 did not undergo a heat treatment, thereby show poor flatness, and was somewhat inferior in accuracy of plate thickness to Examples B1 and B2.
- Comparative Example B4 whose heat treatment had been performed at a temperature higher than the range specified in the fifth embodiment of the present invention, was thereby inferior in cutting property.
- This experimental example relates to the sixth embodiment of the present invention.
- the experimental example used 3000 series Al-Mn alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 23B to 26B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- the slabs were further subjected to a treatment in a heat treatment step, in which they were held at a temperature of 350°C for 4 hours.
- sliced samples and hot-rolled samples were prepared from the thermally treated slabs.
- the sliced samples were prepared by slicing the slabs in a slicing step, while the hot-rolled samples were prepared by subj ecting the slabs to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the sixth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 23B and 24B correspond to examples according to the sixth embodiment of the present invention.
- the sliced samples and hot-rolled samples after the treatments were subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, a strength test, and an anodizability evaluation test.
- the samples using Alloys 23B to 26B had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
- the sample using Alloy 25B contained Mn in a content less than the lower limit in the material aluminum alloy and thereby had insufficient strength.
- the sample using Alloy 26B contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization.
- the samples using Alloys 23B to 26B did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 23B to 26B suffered from accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them were somewhat inferior in accuracy of plate thickness to the corresponding sliced samples.
- the sample using Alloy 25B contained Mn in a content of less than the lower limit in the material aluminum alloy and was thereby somewhat inferior in strength to the other hot-rolled samples.
- the sample using Alloy 26B contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization.
- the samples using Alloys 23B to 26B suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the seventh embodiment of the present invention.
- the experimental example used 6000 series Al-Mg-Si alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 27B to 32B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- the slabs were further subjected to a treatment in a heat treatment step, in which they were held at a temperature of 350°C for 4 hours.
- sliced samples and hot-rolled samples were prepared from the thermally treated slabs. The sliced samples were prepared by slicing the slabs in a slicing step, while the hot-rolled samples were prepared by subj ecting the slabs to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 520°C and subsequently to an aging treatment at 175°C for 8 hours.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the seventh embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 27B and 28B correspond to examples according to the seventh embodiment of the present invention.
- the samples using Alloys 29B and 31B contained Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the sample using Alloy 30B contained Si in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization.
- the sample using Alloy 32B contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency.
- the samples using Alloys 27B to 32B did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 29B and 31B contained Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the sample using Alloy 30B contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surfaces after anodization.
- the sample using Alloy 32B contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency.
- the samples using Alloys 27B to 32B suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the eighth embodiment of the present invention.
- the experimental example used 7000 series Al-Zn-Mg alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 33B to 38B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- the slabs were further subjected to a treatment in a heat treatment step, in which they were held at a temperature of 300°C for 4 hours.
- sliced samples and hot-rolled samples were prepared from the thermally treated slabs. The sliced samples were prepared by slicing the slabs in a slicing step, while the hot-rolled samples were prepared by subj ecting the slabs to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 470°C and subsequently to an aging treatment at 120°C for 48 hours.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the eighth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 33B and 34B correspond to examples according to the eighth embodiment of the present invention.
- the samples using Alloy 35B and 37B contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the samples using Alloys 36B and 38B contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and suffered from unevenness in their appearances of surfaces after anodization.
- the samples using Alloys 33B to 38B did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 35B and 37B contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the samples using Alloys 36B and 38B contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and thereby suffered from unevenness in their appearances of surfaces after anodization.
- This experimental example relates to the ninth embodiment of the present invention.
- the experimental example used 5000 series Al-Mg alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 1C to 22C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- sliced samples and hot-rolled samples were prepared from the slabs.
- the sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 350°C for 4 hours.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the ninth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 1C to 22C correspond to examples according to the ninth embodiment of the present invention.
- the average crystal grain sizes of the thick plates were determined in the same manner as in First Experimental Example, because the crystal grain size of a thick plate affects the anodizability thereof.
- Table 22 shows the test results of the sliced samples, in which the samples using Alloys 1C to 12C correspond to examples according to the ninth embodiment of the present invention; while the samples using Alloys 13C to 22C correspond to comparative examples.
- Table 23 shows the test results of the hot-rolled samples, in which all the samples using Alloys 1C to 22C correspond to comparative examples.
- the samples using Alloys 1C to 13C and 15C to 22C had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
- the sample using Alloy 14C contained Mg in a content of more than the upper limit in the material aluminum alloy, suffered from casting cracks, and was unproducible.
- the sample using Alloy 13C contained Mg in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
- the samples using Alloys 1C to 13C, 17C, and 20C to 22C did not suffer from unevenness in their appearances of surfaces after anodization
- the samples using Alloys 15C, 16C, 18C, and 19C contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization.
- the samples using Alloys 1C to 13C and 15C to 22C did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 17C, 20C, 21C, and 22C contained Cu, Zn, Ti, and Zr, respectively, in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency.
- the samples using Alloy 15C, 16C, 18C, and 19C contain Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization.
- This experimental example relates to the ninth embodiment of the present invention.
- the experimental example used Alloy 3C in Table 21.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloy 3C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- the slabs were subjected to a slicing step to give sliced samples.
- the sliced samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were further subjected to a heat treatment step, in which they were subjected to a heat treatment under conditions given in Table 24.
- Samples C1 and C2, whose heat treatment conditions satisfy the conditions specified in the ninth embodiment of the present invention, correspond to examples according to the ninth embodiment of the present invention; while Samples C3 to C5, whose heat treatment conditions do not satisfy the conditions specified in the ninth embodiment of the present invention, correspond to comparative examples.
- the sliced samples after the treatments were subjected to a flatness evaluation test and an evaluation test for accuracy of plate thickness.
- the evaluation test for accuracy of plate thickness is as in First Experimental Example.
- the cutting property evaluation test is as in Seventh Experimental Example.
- Examples C1 and C2 whose heat treatment conditions satisfy the conditions specified in the ninth embodiment of the present invention, excelled in flatness, accuracy of plate thickness, and cutting property.
- Comparative Example C4 had been thermally treated at a temperature higher than the range specified in the ninth embodiment of the present invention and thereby showed poor cutting property.
- Comparative Example C5 had been thermally treated at a temperature lower than the range specified in the ninth embodiment of the present invention, thereby showed poor flatness, and was somewhat inferior in accuracy of plate thickness to Examples C1 and C2.
- This experimental example relates to the tenth embodiment of the present invention.
- the experimental example used 3000 series Al-Mn alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 23C to 26C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- sliced samples and hot-rolled samples were prepared from the slabs.
- the sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 350°C for 4 hours.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the tenth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 23C and 24C correspond to examples according to the tenth embodiment of the present invention.
- the sliced samples and hot-rolled samples after the treatments were subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, a strength test, and an anodizability evaluation test.
- the samples using Alloys 23C to 26C had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
- the sample using Alloy 25C contained Mn in a content less than the lower limit in the material aluminum alloy and thereby had insufficient strength.
- the sample using Alloy 26C contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization.
- the samples using Alloys 23C to 26C did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 23C to 26C suffered from accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them were somewhat inferior in accuracy of plate thickness to the corresponding sliced samples.
- the sample using Alloy 25C contained Mn in a content of less than the lower limit in the material aluminum alloy and was thereby somewhat inferior in strength to the other hot-rolled samples.
- the sample using Alloy 26C contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization.
- the samples using Alloys 23C to 26C suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the eleventh embodiment of the present invention.
- the experimental example used 6000 series Al-Mg-Si alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 27C to 32C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- sliced samples and hot-rolled samples were prepared from the slabs.
- the sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subj ecting the slabs to a heat treatment and subsequently to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 350°C for 4 hours.
- the resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 520°C and subsequently to an aging treatment at 175°C for 8 hours.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the eleventh embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 27C and 28C correspond to examples according to the eleventh embodiment of the present invention.
- the samples using Alloys 29C and 31C contained Si and Mg, respectively, in a content of less than its lower limit in the material aluminum alloy and showed insufficient strength.
- the sample using Alloy 30C contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization.
- the sample using Alloy 32C contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency.
- the samples using Alloys 27C to 32C did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 29C and 31C contain Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy, and showed insufficient strength.
- the sample using Alloy 30C contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization.
- the sample using Alloy 32C contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency.
- the samples using Alloy 27C to 32C suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the twelfth embodiment of the present invention.
- the experimental example used 7000 series Al-Zn-Mg alloys as the aluminum alloys.
- a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 33C to 38C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
- sliced samples and hot-rolled samples were prepared from the slabs.
- the sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling.
- the sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
- the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 300°C for 4 hours.
- the resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 470°C and subsequently to an aging treatment at 120°C for 48 hours.
- the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the twelfth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not.
- the sliced samples using Alloys 33C and 34C correspond to examples according to the twelfth embodiment of the present invention.
- the samples using Alloys 35C and 37C contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy, and showed insufficient strength.
- the samples using Alloys 36C and 38C contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminumalloy, and thereby suf fered fromunevenness in their appearances of surfaces after anodization.
- the samples using Alloys 33C to 38C did not suffer from unevenness in their appearances of cross sections after anodization.
- the samples using Alloys 35C and 37C contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy, and thereby showed insufficient strength.
- the samples using Alloys 36C and 38C contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and thereby suffered from unevenness in their appearances of surfaces after anodization.
- Methods for manufacturing aluminum alloy thick plates show superior productivity, can easily control the surface condition and flatness to improve the accuracy of plate thickness, and are thereby industrially very useful.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Acoustics & Sound (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Casting Support Devices, Ladles, And Melt Control Thereby (AREA)
- Continuous Casting (AREA)
Abstract
Description
- The present invention relates to methods for manufacturing aluminum alloy thick plates, and the resulting aluminum alloy thick plates.
- Aluminum alloy materials such as aluminum alloy thick plates are generally used for various applications including semiconductor-related devices such as base substrates, transport devices, and vacuum chambers; electrical and electronic parts and their manufacturing devices; household articles; and mechanical parts.
- Such aluminum alloy materials are generally manufactured by melting aluminum alloy ingots, and casting the molten material to give a slab, conducting a heat treatment for homogenization, if necessary, and then rolling the slab to a predetermined thickness (see, for example, Paragraphs 0037 to 0045 of Patent Document 1).
- As mold materials used for press molds, steels and cast steel are typically used for mass production, while zinc alloy cast materials and aluminum alloy cast materials are used for prototype production. In recent years, there has been a trend of producing multiple varieties in small amounts, and therefore ductile materials such as rolled or forged aluminum alloys are widely spread for middle-to-small-scale production.
- Patent Document 1: Japanese Unexamined Patent Application Publication (JP-A) No.
2005-344173 - However, the method for manufacturing aluminum alloy materials by rolling has the following problems:
- (1) In the method in which rolling is carried out after casting, control of the surface condition and flatness (especially the flatness in the longitudinal direction) of the rolled plate is carried out only by pressure rolls, and a thick oxide film is generated on the surface of the rolled plate by hot rolling, and controlling the surface condition and flatness is difficult.
- (2) Since it is difficult to control the thickness of the plate by pressure rolls, it is difficult to improve the accuracy of plate thickness; the size of intermetallic compounds increases at the center of the thickness direction of the plate, and thus when anodization is conducted, the surface and cross section in the thickness direction of the plate often suffer from unevenness. Additionally, when a slab is rolled, the number of operation steps increases with an increasing number of rolling procedures, whereby the cost is disadvantageously increased.
- Under these circumstances, the present invention has been made and an object thereof is to provide a method for manufacturing an aluminum alloy thick plate, which method enables improved accuracy of plate thickness with high productivity and good controllability of surface condition and flatness, and to provide an aluminum alloy thick plate which is manufactured by the procedures of the manufacturing method and excels in surface condition, flatness, and accuracy of plate thickness.
- According to a first embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0. 3 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 400°C or higher but lower than its melting point for one hour or longer.
- According to a second embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 400°C or higher but lower than its melting point for one hour or longer.
- According to a third embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further containing at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0.6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 400°C or higher but lower than its melting point for one hour or longer.
- According to a fourth embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 350°C or higher but lower than its melting point for one hour or longer.
- In the first to fourth embodiments of the present invention, the following configurations are preferred:
- (A) Subsequent to the heat treatment step, the surface of the aluminum alloy thick plate is subjected to a surface smoothing treatment, as a surface smoothing treatment step. In this configuration, the surface smoothing treatment is preferably carried out by at least one process selected from the group consisting of cutting, grinding, and polishing.
- (B) In the slicing step, a central portion in a thickness direction is removed from the slab, in which the central portion has two substantially identical thicknesses in the thickness direction from the center of the thickness direction to the both surfaces of the central portion, respectively, and has a total thickness of from one-thirtieth to one-fifth the thickness T of the slab (T/30 to T/5).
- According to a fifth embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer; and a slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness.
- According to a sixth embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer; and a slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness.
- According to a seventh embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further containing at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0.6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer; and a slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness.
- According to an eighth embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 350°C for one hour or longer; and a slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness.
- In the fifth to eighth embodiments of the present invention, the following configurations are preferred:
- (C) Subsequent to the slicing step, the surface of the aluminum alloy thick plate having a predetermined thickness is subjected to a surface smoothing treatment, as a surface smoothing treatment step. In this configuration, the surface smoothing treatment is preferably carried out by at least one process selected from the group consisting of cutting, grinding, and polishing.
- (D) In the slicing step, a central portion in a thickness direction is removed from the slab, in which the central portion has two substantially identical thicknesses in the thickness direction from the center of the thickness direction to the both surfaces of the central portion, respectively, and has a total thickness of from one-thirtieth to one-fifth the thickness T of the slab (T/30 to T/5).
- According to a ninth embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer.
- According to a tenth embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer.
- According to an eleventh embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further containing at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0.6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer.
- According to a twelfth embodiment of the present invention, there is provided a method for manufacturing an aluminum alloy thick plate from an aluminum alloy, the aluminum alloy containing Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities. The method includes in the following order: a melting step of melting the aluminum alloy; a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy; a filtration step of filtering the aluminum alloy, from which hydrogen gas has been removed, to remove inclusions from the aluminum alloy; a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab; a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; and a heat treatment step of thermally treating the aluminum alloy thickplate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 350°C for one hour or longer.
- In the ninth to twelfth embodiments of the present invention, the following configurations are preferred:
- (E) Subsequent to the heat treatment step, the surface of the aluminum alloy thick plate is subjected to a surface smoothing treatment, as a surface smoothing treatment step. In this configuration, the surface smoothing treatment is preferably carried out by at least one process selected from the group consisting of cutting, grinding, and polishing.
- (F) In the slicing step, a central portion in a thickness direction is removed from the slab, in which the central portion has two substantially identical thicknesses in the thickness direction from the center of the thickness direction to the both surfaces of the central portion, respectively, and has a total thickness of from one-thirtieth to one-fifth the thickness T of the slab (T/30 to T/5).
- According to a thirteenth embodiment of the present invention, there is provided an aluminum alloy thick plate which is manufactured by the method for manufacturing an aluminum alloy thick plate, according to any one of the first to twelfth embodiments of the present invention, and includes crystal grains having an average grain size of 400 µm or less.
- According to the first to fourth embodiments of the present invention, the resulting aluminum alloy thick plate includes finer intermetallic compounds and has improved strength, because the material aluminum alloy has contents of predetermined elements controlled within predetermined ranges. The hydrogen gas removal step removes hydrogen to thereby control the concentration of hydrogen in the slab. Therefore, even if crystal grains in the slab become coarse, hydrogen is not accumulated or enriched at the grain boundary near the surface of the slab. This suppresses blistering of the slab and peeling of the aluminum alloy thick plate resulting from the blistering, and also suppresses potential defects on the surface of the thick plates which appear as surface defects of the thick plate. The aluminum alloy thick plate has improved strength. The filtration step removes inclusions such as oxides and non-metals from the aluminum alloy. Slicing the slab in the slicing step reduces the thickness of the oxide film; improves the surface condition, flatness and accuracy of the plate thickness of the aluminum alloy thick plate; and also improves its productivity. In addition, the heat treatment step thermally treats the aluminum alloy thick plate to thereby remove the internal stress of the aluminum alloy and uniformize its inner structure.
- According to the first to fourth embodiments of the present invention, therefore, the aluminum alloy thick plate can have improved strength. The aluminum alloy thick plate is manufactured by slicing a slab, and this eliminates necessity to reduce its thickness by hot rolling unlike in known aluminum alloy thick plates. This simplifies operation steps and thereby improves the productivity. This also eliminates unevenness (uneven color) of the surface and cross section of the thick plate; and improves the flatness, surface condition after anodization, and accuracy of plate thickness. By thermally treating the sliced aluminum alloy thick plate having a predetermined thickness at a temperature of 400°C (or 350°C) or higher but lower than its melting point, the internal stress of the aluminum alloy thick plate can be removed and its inner structure can be uniformized. Thus, the aluminum alloy thick plate can have good flatness and satisfactory accuracy of plate thickness and can maintain its satisfactory strength.
- The configuration (A) helps to further improve the surface condition and flatness of the aluminum alloy thick plate and eliminates the gas accumulation of the surface of the thick plate, because the surface is further smoothened. The resulting aluminum alloy thick plate, if used as a vacuum chamber, can provide an improved degree of vacuum.
- The configuration (B) helps to provide an aluminum alloy thick plate excellent in appearance quality even after anodization, because the central portion of the slab is removed, which central portion will often cause unevenness in the surface and cross section of the aluminum alloy thick plate after anodization. This configuration also helps to reduce the within-lot variation.
- According to the fifth to eighth embodiments of the present invention, the aluminum alloy thick plate can include finer intermetallic compounds andhavehigher strength, because the material aluminum alloy has contents of predetermined elements controlled within predetermined ranges. The hydrogen gas removal step removes hydrogen gas to thereby control the concentration of hydrogen in the slab. Therefore, even if crystal grains in the slab become coarse, hydrogen is not accumulated or enriched at the grain boundary near the surface of the slab. This suppresses blistering of the slab and peeling of the aluminum alloy thick plate resulting from the blistering; suppresses potential defects on the surface of the thick plates which appear as surface defects of the thick plat; and improves the strength of the aluminum alloy thick plate. The filtration step removes inclusions such as oxides and non-metals from the aluminum alloy. The heat treatment step thermally treats the slab to eliminate the internal stress and to uniformize the inner structure thereof. The slicing step slices the slab so as to reduce the thickness of the oxide film and to improve the surface condition, flatness and accuracy of the plate thickness of the aluminum alloy thick plate, as well as its productivity.
- According to the fifth to eighth embodiments of the present invention, therefore, the aluminum alloy thick plate can have improved balance among its flatness, strength, and cutting property. Specifically, the heat treatment at a temperature of 200°C or higher but lower than 400°C (or 350°C) applied to the slab suppresses the increase in ductility. This helps to remove the internal stress and to uniformize the inner structure of the thick plate without adversely affecting the cutting property (chip breakability). The resulting aluminum alloy thick plate can thereby have good flatness and satisfactory accuracy of plate thickness and can maintain its satisfactory strength. The aluminum alloy thick plate is manufactured by slicing a slab. This eliminates necessity to reduce its thickness by hot rolling unlike in known aluminum alloy thick plates; simplifies operation steps and improves the productivity; and also eliminates surface unevenness (uneven color) of the cross section of the thick plate and improves the flatness, quality of appearance after anodization, and accuracy of plate thickness.
- The configuration (C) helps to further improve the surface condition and flatness of the aluminum alloy thick plate and eliminates the gas accumulation of the surface of the thick plate, because the surface is further smoothened. The resulting aluminum alloy thick plate, if used as a vacuum chamber, can provide an improved degree of vacuum.
- The configuration (D) helps to provide an aluminum alloy thick plate excellent in appearance quality even after anodization, because the central portion of the slab is removed, which central portion will often cause unevenness in the surface and cross section of the aluminum alloy thick plate after anodization. This configuration also helps to reduce the within-lot variation.
- According to the ninth to twelfth embodiments of the present invention, the aluminum alloy thick plate includes finer intermetallic compounds and has improved strength, because the material aluminum alloy has contents of predetermined elements controlled within predetermined ranges. The hydrogen gas removal step removes hydrogen to thereby control the concentration of hydrogen in the slab. Therefore, even if crystal grains in the slab become coarse, hydrogen is not accumulated or enriched at the grain boundary near the surface of the slab. This suppresses blistering of the slab and peeling of the aluminum alloy thick plate resulting from the blistering; suppresses potential defects on the surface of the thick plates which appear as surface defects of the thick plate; and improves the strength of the aluminum alloy thick plate. The filtering step removes inclusions such as oxides and non-metals from the aluminum alloy. Slicing the slab in the slicing step reduces the thickness of the oxide film; improves the surface condition, flatness and accuracy of the plate thickness of the aluminum alloy thick plate; and improves the productivity of the aluminum alloy thick plate. In addition, the heat treatment step thermally treats the aluminum alloy thick plate to thereby remove the internal stress of the aluminum alloy and uniformize its inner structure.
- According to the ninth to twelfth embodiments of the present invention, therefore, the aluminum alloy thick plate can have improved strength. The aluminum alloy thick plate is manufactured by slicing a slab, and this eliminates necessity to reduce its thickness by hot rolling unlike in known aluminum alloy thick plates. This simplifies operation steps; improves the productivity; eliminates unevenness (uneven color) of the surface and cross section of the thick plate; and improves the flatness, quality of appearance after anodization, and accuracy of plate thickness. Further, this also improves the balance among the flatness, strength, and cutting property of the aluminum alloy thick plate. The heat treatment at a temperature of 200°C or higher but lower than 400°C (or 350°C) applied to the sliced aluminum alloy thick plate having a predetermined thickness suppresses the increase in ductility, whereby helps to remove the internal stress and uniformize the inner structure of the aluminum alloy thick plate without adversely affecting the cutting property (chip breakability). The resulting aluminum alloy thick plate can thereby have good flatness and satisfactory accuracy of plate thickness and maintain its satisfactory strength.
- The configuration (E) helps to further improve the surface condition and flatness of the aluminum alloy thick plate and eliminates the gas accumulation of the surface of the thick plate, because the surface is further smoothened. The resulting aluminum alloy thick plate, if used as a vacuum chamber, can provide an improved degree of vacuum.
- The configuration (F) helps to provide an aluminum alloy thick plate excellent in appearance quality even after anodization, because the central portion of the slab is removed, which central portion will often cause unevenness in the surface and cross section of the aluminum alloy thick plate after anodization. This configuration also helps to reduce the within-lot variation.
- The aluminum alloy thick plates according to the thirteenth embodiment of the present invention excel in surface condition, flatness, and accuracy of plate thickness. They also have high quality, because their surface is smoothened and thereby is free from gas accumulation. They can be used in a wide variety of applications and can be recycled and used for other applications, because the surface appearance of them after anodization is substantially free from unevenness.
-
- [
Fig. 1] Fig. 1 is a flow chart of methods for manufacturing an aluminum alloy thick plate, according to the first to fourth embodiments and the ninth to twelfth embodiments of the present invention. - [
Fig. 2] Fig. 2 is a schematic view showing a central portion in a thickness direction of the slab to be removed in the slicing step. - [
Fig. 3] Fig. 3 is a flow chart of methods for manufacturing an aluminum alloy thick plate, according to the fifth to eighth embodiments of the present invention. -
- S1
- melting step
- S2
- hydrogen gas removal step
- S3
- filtration step
- S4
- casting step
- S5
- slicing step or heat treatment step
- S6
- heat treatment step or slicing step
- S7
- surface smoothing treatment step
- A
- center of thickness direction
- B
- central portion in thickness direction
- T
- thickness
- 1
- slab
- Methods for manufacturing aluminum alloy thick plates and resulting aluminum alloy thick plates, according to the present invention, will be illustrated in detail with reference to the attached drawings. The present invention will be illustrated below while being categorized as (A) the first to fourth embodiments of the present invention, (B) the fifth to eighth embodiments of the present invention, (C) the ninth to twelfth embodiments of the present invention, and (D) the thirteenth embodiment of the present invention.
- With reference to
Fig. 1 , the methods for manufacturing an aluminum alloy thick plate (hereinafter also referred to as "thick plate" for the sake of convenience), according to the first to fourth embodiments of the present invention, each include a melting step (S1), a hydrogen gas removal step (S2), a filtration step (S3), a casting step (S4), a slicing step (S5), and a heat treatment step (S6) in this order. The methods may further include, where necessary, a surface smoothing treatment step (S7) subsequent to the heat treatment step (S6). - In these manufacturing methods, initially, aluminum alloy ingots are melted in the melting step (S1). Next, hydrogen gas is removed from the molten aluminum alloy in the hydrogen gas removal step (S2), and inclusions such as oxides and non-metals are removed therefrom in the filtration step (S3). Next, the resulting aluminum alloy is cast into a slab in the casting step (S4). The slab is then sliced into an aluminum alloy thick plate having a predetermined thickness in the slicing step (S5). The aluminum alloy thick plate having a predetermined thickness is then subjected to a heat treatment in the heat treatment step (S6) and, where necessary, subjected to a surface smoothing treatment in the surface smoothing treatment step (S7).
- The manufacturing methods according to the first, second, third, and fourth embodiments of the present invention use a 5000 series Al-Mg alloy, a 3000 series Al-Mn alloy, a 6000 series Al-Mg-Si alloy, and a 7000 series Al-Zn-Mg alloy, respectively, as a raw material aluminum alloy. The details of them are as follows.
- According to the first embodiment of the present invention, a 5000 series Al-Mg alloy is used. The aluminum alloy contains Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further contains at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0. 3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- The reasons why the contents of the respective components are specified will be described below.
- Magnesium (Mg) serves to improve the strength of the aluminum alloy. Mg, if its content is less than 1.5 percent by mass, may not exhibit the activity sufficiently. In contrast, Mg, if its content is more than 12.0 percent by mass, may significantly adversely affect the casting ability, and this may impede the manufacture of the product. Accordingly, the Mg content should be 1.5 percent by mass or more and 12.0 percent by mass or less.
- Silicon (Si) serves to improve the strength of the aluminum alloy. Si is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al- (Fe) - (Mn) -Si intermetallic compound together with Mn and Fe in the slab typically in the casting step (S4). Si, if its content is more than 0.7 percent by mass, may cause a coarse intermetallic compound in the slab to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Si content should be 0.7 percent by mass or less.
- Iron (Fe) allows crystal grains of the aluminum alloy to be finer and more stabilized and allows the aluminum alloy to have improved strength. Fe is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al-Fe- (Mn) - (Si) intermetallic compound together with Mn and/or Si in the slab typically in the casting step (S4). Fe, if its content is more than 0.8 percent by mass, may cause a coarse intermetallic compound in the slab to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Fe content should be 0.8 percent by mass or less.
- Copper (Cu) serves to improve the strength of the aluminum alloy. However, a Cu content of 0.6 percent by mass is enough to ensure a sufficient strength to be used endurably as a thick plate. Accordingly, the Cu content should be 0.6 percent by mass or less.
- Manganese (Mn) is solidly dissolved in the aluminum alloy and thereby serves to improve the strength of the aluminum alloy. Mn, if its content is more than 1.0 percent by mass, may cause a coarse intermetallic compound to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Mn content should be 1.0 percent by mass or less.
- Chromium (Cr) serves to suppress the grain growth by depositing as a fine compound in the casting step (S4) and heat treatment step (S6). Cr, if its content is more than 0.5 percent by mass, may cause a coarse Al-Cr intermetallic compound as a primary crystal to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Cr content should be 0.5 percent by mass or less.
- Zinc (Zn) serves to improve the strength of the aluminum alloy. However, a Zn content of 0.4 percent by mass is enough to ensure a sufficient strength to be used endurably as a thick plate. Accordingly, the Zn content should be 0.4 percent by mass or less.
- Titanium (Ti) allows the slab to contain finer crystal grains. If the Ti content is more than 0.1 percent by mass, the activity may be saturated. Accordingly, the Ti content should be 0.1 percent by mass or less.
- Zirconium (Zr) allows the slab to contain finer crystal grains. If the Zr content is more than 0.3 percent by mass, the activity may be saturated. Accordingly, the Zr content should be 0.3 percent by mass or less.
- The aluminum alloy contains the above-mentioned components, with the remainder being aluminum and inevitable impurities. Exemplary inevitable impurities include V and B. Each of such impurities, if its content is 0.01 percent by mass or less, will not affect the characteristic properties of the aluminum alloy thick plates according to the present invention.
- According to the second embodiment of the present invention, a 3000 series Al-Mn alloy is used. The aluminum alloy contains Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further contains at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- The reasons why the contents of the respective components are specified will be described below.
The reasons why the Si, Fe, Cu, Cr, Zn, Ti, and Zr contents are specified and the description on inevitable impurities are as with the Al-Mg alloy, and the description thereof is herein omitted. - Manganese (Mn) is solidly dissolved in the aluminum alloy and thereby serves to improve the strength of the aluminum alloy. Mn, if its content is less than 0.3 percent by mass, maynot exhibit the activity sufficiently. In contrast, Mn, if its content is more than 1.6 percent by mass, may cause a coarse intermetallic compound, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Mn content should be 0.3 percent by mass or more and 1.6 percent by mass or less.
- Magnesium (Mg) serves to improve the strength of the aluminum alloy. However, aMg content of 1. 5percentbymass is enough to ensure a sufficient strength to be used endurably as a thick plate. Accordingly, the Mg content should be 1.5 percent by mass or less.
- According to the third embodiment of the present invention, a 6000 series Al-Mg-Si alloy is used. The aluminum alloy contains Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further contains at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0.6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- The reasons why the contents of the respective components are specified will be described below.
The reasons why the Fe, Mn, Cr, Ti, and Zr contents are specified and the description on the inevitable impurities are as with the Al-Mg alloy, and the description thereof is herein omitted. - Silicon (Si) serves to improve the strength of the aluminum alloy. Si is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al-(Fe)-Si intermetallic compound and a Si intermetallic compound in the slab typically in the casting step (S4). Si, if its content is less than 0.2 percent by mass, may not exhibit the activity sufficiently. In contrast, Si, if its content is more than 1.6 percent by mass, may cause a coarse Si intermetallic compound in the slab, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Si content should be 0.2 percent by mass or more and 1.6 percent by mass or less.
- Magnesium (Mg) forms Mg2Si in the coexistence with Si to thereby serve to improve the strength of the aluminum alloy. Mg, if its content is less than 0.3 percent by mass, may not exhibit the activity sufficiently. In contrast, if the Mg content is more than 1.5 percent by mass, the activity may be saturated. Accordingly, the Mg content should be 0.3 percent by mass or more and 1.5 percent by mass or less.
- Copper (Cu) serves to improve the strength of the aluminum alloy. Cu, if its content is more than 1.0 percent by mass, may impair the corrosion resistance. Accordingly, the Cu content should be 1.0 percent by mass or less.
- Zn serves to improve the strength of the aluminum alloy. Zn, if its content is more than 0.4 percent by mass, may impair the corrosion resistance. Accordingly, the Zn content should be 0.4 percent by mass or less.
- According to the fourth embodiment of the present invention, a 7000 series Al-Zn-Mg alloy is used. The aluminum alloy contains Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9.0 percent by mass or less, and further contains at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities.
- The reasons why the contents of the respective components are specified will be described below.
The reasons why the Cr, Ti, and Zr contents are specified and the description of the inevitable impurities are as with the Al-Mg alloy, whereby the descriptions thereof are herein omitted. - Magnesium (Mg) serves to improve the strength of the aluminum alloy. Mg, if its content is less than 0.4 percent by mass, may not exhibit the activity sufficiently. In contrast, Mg, if its content is more than 4.0 percent by mass, may often cause unevenness in the surface appearance after anodization. Accordingly, the Mg content should be 0.4 percent by mass or more and 4.0 percent by mass or less.
- Zinc (Zn) serves to improve the strength of the aluminum alloy. Zn, if its content is less than 3.0 percent by mass, may not exhibit the activity sufficiently. In contrast, Zn, if its content is more than 9. 0 percent by mass, may often cause unevenness in the surface appearance after anodization. Accordingly, the Zn content should be 3.0 percent by mass or more and 9.0 percent by mass or less.
- Silicon (Si) is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al-(Fe)-Si intermetallic compound in the slab typically in the casting step (S4). Si, if its content is more than 0.7 percent by mass, may cause a coarse Al- (Fe) -Si intermetallic compound in the slab, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Si content should be 0.7 percent by mass or less.
- Iron (Fe) is generally contained in the aluminum alloy as an impurity in the ingot and forms an Al-Fe intermetallic compound in the slab typically in the casting step (S4). Fe, if its content is more than 0.8 percent by mass, may cause a coarse Al-Fe intermetallic compound in the slab, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Fe content should be 0.8 percent by mass or less.
- Copper (Cu) serves to improve the strength of the aluminum alloy. Cu, if its content is more than 3.0 percent by mass, may impair the corrosion resistance. Accordingly, the Cu content should be 3.0 percent by mass or less.
- Manganese (Mn) allows the crystal structure to be finer. Mn, if its content is more than 0.8 percent by mass, may cause a coarse intermetallic compound, to thereby often cause unevenness in the surface appearance after anodization. Accordingly, the Mn content should be 0.8 percent by mass or less.
- Next, the respective steps in the manufacturing methods according to the first to fourth embodiments of the present invention will be described.
- The melting step (S1) is a step of melting the raw material aluminum alloy.
- The hydrogen gas removal step (S2) is a step of removing hydrogen gas from the aluminum alloy which has been melted in the melting step (S1).
- Hydrogen gas is generated typically from hydrogen in a fuel and from water and organic substances attached typically to the ingot. Hydrogen gas, if contained in a large content, will cause the following disadvantages.
- [a] Pin holes are generated.
- [b] The product has insufficient strength.
- [c] Hydrogen is accumulated and enriched at the grain boundary in the vicinity of the surface of the slab. This causes blistering of the slab and peeling of the aluminum alloy thick plate resulting from the blistering; and also causes potential defects on the surface of the thick plate which appear as surface defects of the thick plate.
- Accordingly, the amount of hydrogen gas is preferably 0.2 ml or less and more preferably 0.1 ml or less per 100 g of the aluminum alloy. Removal of hydrogen gas can be suitably carried out by subjecting a moltenmetal typically to a fluxing process, chlorine refining, or in-line refining, and it can be more suitably carried out by using a SNIF (spinning nozzle inert flotation) system and a porous plug (see
JP-ANo. 2002-146447 - The concentration of hydrogen gas in a slab can be determined typically in the following manner. Specifically, a sample is cut out from the slab after the casting step; then subj ected to ultrasonic cleaning with alcohol and acetone; and thereafter analyzed typically according to the inert gas fusion thermal conductivity method (LIS A06-1993).
- The concentration of hydrogen gas in an aluminum alloy thick plate can be determined typically in the following manner. Specifically, a sample is cut out from the aluminum alloy thick plate. Next, the sample is immersed in an aqueous NaOH solution; then treated with nitric acid to remove an oxide film on the surface of the sample; and the treated sample is subjected to ultrasonic cleaning with alcohol and acetone and then analyzed according typically to the vacuum heat extraction capacitance method (LIS A06-1993).
- The filtration step (S3) is a step of removing mainly oxide and non-metal inclusions from the aluminum alloy with a filtrating device. The filtrating device is provided typically with a ceramic tube with alumina particles of about 1 mm. The inclusions are removed by allowing a molten metal to pass through the ceramic tube.
- The hydrogen gas removal step and the filtration step ensure high quality of the aluminum alloy, and the resulting aluminum alloy is made into a high-quality slab in the subsequent casting step (S4). These steps can suppress the generation of deposits of oxides (dross), and this reduces the effort and time for removing the dross.
- The casting step (S4) is a step of producing a slab by forming a molten metal of the aluminum alloy typically with a casting apparatus into a predetermined shape such as a rectangular parallelepiped and solidifying the metal. Typically, a casting apparatus equipped with a water-cooled mold is used. A semi-continuous casting process may be employed as the casting process. In the semi-continuous castingprocess, a molten metal of the aluminum alloy is injected from above into a water-cooled metallic mold having an open bottom, and the solidified aluminum alloy is successively withdrawn from the bottom of the water-cooled mold to give slabs having predetermined thickness. The semi-continuous casting process may be carried out vertically or horizontally.
- The slicing step (S5) is a step of producing an aluminum alloy thick plate having a predetermined thickness by slicing the slab produced in the casting step (S4). The slab slicing process may be employed as a slicing process. The slab slicing process is a process for cutting out the slab in the cast direction by slicing the slab produced by the semi-continuous casting process typically with a band saw cutting apparatus, to give an aluminum alloy thick plate having a predetermined thickness. The thickness of the aluminum alloy thick plate is preferably 15 to 200 mm, but it is not particularly limited, and can be varied suitably depending on the intended use of the aluminum alloy thick plate.
- A band saw is preferably used in the slicing process, but it is not particularly limited, and cutting may be also performed typically with a circular saw cutting apparatus, or by laser or water pressure.
- Slicing the slab gives an aluminum alloy thick plate superior typically in surface condition, flatness, and accuracy of the plate thickness to a rolled product. For example, there can be obtained a thick plate having a flatness (amount of warpage) per 1 m in the casting direction of 0.4 mm or less per 1 m length in the evaluation of flatness, and the accuracy of the plate thickness of ±100 µm or less.
- With reference to
Fig. 2 , a central portion B shaded with slanted lines is preferably removed in the slicing step (S5). The central portion B has two substantially identical thicknesses in a thickness direction from the center of the thickness direction A to the both surfaces of the central portion, respectively, and has a total thickness of from one-thirtieth to one-fifth the thickness T of the slab 1 (T/30 to T/5). The central portion B inFig. 2 is illustrated to have a thickness about one-fifth the thickness T. The thicknesses b1 and b2 of the upper and lower portions of the central portion B of theslab 1 are preferably equal to each other, but a difference between them of about 30% is acceptable. As used herein "the center of the thickness direction A" refers to a location which is the center of theslab 1 in the thickness direction and is located about a half the thickness T of theslab 1, i.e., a location of theslab 1 about T/2 deep. - The central portion B of the
slab 1 is susceptive to unevenness in the surface and cross section of the thick plate after anodization. However, when the central portion B is removed by the slicing step (S5), and a thick plate excellent in quality of appearance after anodization with less within-lot variation can be obtained. Removal of a central portion having a thickness of less than T/30 (one-thirtieth the thickness T) may often cause a thick plate suffering from unevenness in the surface appearance after anodization and often cause a large within-lot variation. In contrast, if a central portion having a thickness of more than T/5 (one-fifth the thickness T) is removed, an excessively large amount of the portion is to be removed, and this may impair the productivity. Accordingly, the central portion B of theslab 1 is preferably removed in such an amount that the central portion has two substantially identical thicknesses in the thickness direction from the center of the thickness direction A to the both surfaces of the central portion, respectively, and has a total thickness of from one-thirtieth to one-fifth the thickness T of the slab 1 (T/30 to T/5). - After slicing the slab in the slicing step (S5), the subsequent heat treatment step (S6) is performed in which a heat treatment is conducted in order to remove the internal stress and to uniformize the inner structure. The heat treatment improves the flatness, accuracy of plate thickness, and quality of appearance after anodization.
- The heat treatment step (S6) is a step of carrying out a heat treatment (heat treatment for homogenization) on the aluminum alloy thick plate having a predetermined thickness produced in the slicing step (S5). The heat treatment may be carried out according to a common procedure. Specifically, when the aluminum alloy is a 5000 series Al-Mg alloy (the first embodiment of the present invention), a 3000 series Al-Mn alloy (the second embodiment of the present invention), and a 6000 series Al-Mg-Si alloy (the third embodiment of the present invention), the heat treatment is performed by holding the aluminum alloy thick plate at a temperature of 400°C or higher but lower than its melting point for one hour or longer. When the aluminum alloy is a 7000 series Al-Zn-Mg alloy (the fourth embodiment of the present invention), the heat treatment is performed by holding the aluminum alloy thick plate at a temperature of 350°C or higher but lower than its melting point for one hour or longer.
- The slicing process of the slab obtained in the casting step (S4) allows the internal residual stress to be released, and this often causes warpage. According to the present invention, however, the sliced aluminum alloy thickplate having a predetermined thickness and subj ected to a heat treatment while being placed typically on a surface plate, and the resulting aluminum alloy thick plate thereby has improved flatness.
- In the first to third embodiments of the present invention, a heat treatment, if conducted at a temperature of lower than 400°C, may not sufficiently help to remove the inner stress and to uniformize a solute element, which is segregated during casting, and the heat treatment may therefore not exhibit sufficient advantages. Accordingly, the treatment temperature herein should be 400°C or higher. If a heat treatment is conducted at a temperature equal to or higher than the melting point, part of the surface of the slab is melted, to cause an internal defect and to impair the strength/ductility. Accordingly, the treatment temperature should be lower than the melting point.
- In the fourth embodiment of the present invention, a heat treatment, if conducted at a temperature of lower than 350°C, may not sufficiently help to remove the inner stress and to uniformize a solute element, which is segregated during casting, and therefore may exhibit less advantages. Accordingly, the treatment temperature herein should be 350°C or higher. If a heat treatment is conducted at a temperature equal to or higher than the melting point, part of the surface of the slab ismelted, to cause an internal defect and to impair the strength/ductility. Accordingly, the treatment temperature should be lower than the melting point.
- A heat treatment, if conducted for a time shorter than one hour, may not sufficiently help intermetallic compounds to be solidly dissolved, and this may often cause the intermetallic compounds to be deposited. Accordingly, the treatment time should be one hour or longer. In contrast, a heat treatment, if conducted for a time of longer than about 8 hours, may be saturated in its effect, and this may cause energy loss. Accordingly, the treatment time is preferably controlled to be 8 hours or shorter.
- The aluminum alloy thick plate after the heat treatment in the heat treatment step (S6) may be subjected to a surface smoothing treatment according to necessity in order to remove crystallized substances and oxides generated on the surface of the thick plate or to eliminate gas accumulation in the surface of the thick plate.
- The surface smoothing treatment step (S7) is a step of subjecting the surface of the aluminum alloy thick plate produced in the heat treatment step (S6) to a surface smoothing treatment. Exemplary surface smoothing treatments include, but are not limited to, cutting such as end mill cutting and diamond bite cutting; grinding which faces the surface typically with a grindstone; and polishing such as buff polishing.
- When the aluminum alloy thick plate is used for a vacuum chamber (chamber for a vacuum apparatus), it is especially effective to carry out a surface smoothing treatment. The reason therefor is as follows. Specifically, a vacuum chamber suffers from a decrease in the degree of vacuum therein caused by, when the chamber is decompressed to attain high vacuum, releasing of adsorbed gas from the inner surface of the chamber and releasing of gas atoms which are solidly dissolved in the thick plate onto the surface. This elongates the time which takes to reach a target degree of vacuum and thereby lowers production efficiency. Accordingly, the following conditions are required for the aluminum alloy thick plate used for a chamber: the amount of gas which adsorbs onto the surface of the thick plate positioned in an inner portion of the chamber is low; and the gas atoms which are solidly dissolved in the thick plate are not released even in high vacuum. The surface smoothing treatment herein satisfies these conditions.
- With reference to
Fig. 3 , the methods for manufacturing an aluminum alloy thick plate, according to the fifth to eighth embodiments of the present invention, each include a melting step (S1), a hydrogen gas removal step (S2), a filtration step (S3), a casting step (S4), a heat treatment step (S5), and a slicing step (S6) in this order. The methods may further include, where necessary, a surface smoothing treatment step (S7) subsequent to the slicing step (S6). - In these manufacturing methods, initially, a raw material aluminum alloy is melted in the melting step (S1). Next, hydrogen gas is removed from the molten aluminum alloy in the hydrogen gas removal step (S2), and inclusions such as oxides and non-metals are removed therefrom in the filtration step (S3). Next, the resulting aluminum alloy is cast into a slab in the casting step (S4). The slab is subjected to a heat treatment in the heat treatment step (S5) and is then sliced into an aluminum alloy thick plate having a predetermined thickness in the slicing step (S6). Where necessary, the aluminum alloy thick plate having a predetermined thickness is further subjected to a surface smoothing treatment in the surface smoothing treatment step (S7).
- The manufacturing methods according to the fifth, sixth, seventh, and eighth embodiments of the present invention use, as a raw material aluminum alloy, a 5000 series Al-Mg alloy, a 3000 series Al-Mn alloy, a 6000 series Al-Mg-Si alloy, and a 7000 series Al-Zn-Mg alloy, respectively. The details of them are as follows.
- A 5000 series Al-Mg alloy as in the first embodiment of the present invention is used in this embodiment. The composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the first embodiment of the present invention.
- A 3000 series Al-Mn alloy as in the second embodiment of the present invention is used in this embodiment. The composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the second embodiment of the present invention.
- A 6000 series Al-Mg-Si alloy as in the third embodiment of the present invention is used in this embodiment. The composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the third embodiment of the present invention.
- A 7000 series Al-Zn-Mg alloy as in the fourth embodiment of the present invention is used in this embodiment. The composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the fourth embodiment of the present invention.
- Next, the respective steps in the manufacturing methods according to the fifth to eighth embodiments of the present invention will be described.
- This step is the same as with the melting step (S1) in the first to fourth embodiments of the present invention.
- This step is the same as with the hydrogen gas removal step (S2) in the first to fourth embodiments of the present invention.
- This step is the same as with the filtration step (S3) in the first to fourth embodiments of the present invention.
- This step is the same as with the casting step (S4) in the first to fourth embodiments of the present invention.
- Before slicing the slab produced in the casting step (S4), a heat treatment is carried out in the subsequent heat treatment step (S5), for the purpose of removing internal stress and uniformizing the inner structure. The heat treatment of the slab helps to improve the flatness, accuracy of plate thickness, and quality of appearance after anodization.
- The heat treatment step (S5) is a step of subj ecting the slab produced in the casting step (S4) to a heat treatment (heat treatment for homogenization). The heat treatment is carried out according to a common procedure. Specifically, when the aluminum alloy is a 5000 series Al-Mg alloy (the fifth embodiment of the present invention), a 3000 series Al-Mn alloy (the sixth embodiment of the present invention), and a 6000 series Al-Mg-Si alloy (the seventh embodiment of the present invention), the heat treatment is performed by holding the slab at a temperature of 200°C or higher but lower than 400°C for one hour or longer. When the aluminum alloy is a 7000 series Al-Zn-Mg alloy (the eighth embodiment of the present invention), the heat treatment is performed by holding the slab at a temperature of 200°C or higher but lower than 350°C for one hour or longer.
- In the fifth to seventh embodiments of the present invention, a heat treatment, if conducted at a temperature of lower than 200°C, may not sufficiently help to remove the inner stress and therefore may not exhibit satisfactory advantages. Accordingly, the treatment temperature should be 200°C or higher. In contrast, a heat treatment, if conducted at a temperature of 400°C or higher, may excessively increase the ductility and lower the strength and cutting property. As used herein the term "cutting property" refers to chip breakability. Chips (scraps) are preferably formed as small or short pieces. This is because long chips become entangled with a working tool (blade) and are rotated therewith, and this damages the surface of the thick plate and breaks the tool. Accordingly, the treatment temperature should be lower than 400°C. A heat treatment performed under above-specified temperature conditions helps to improve the flatness and accuracy of plate thickness without adversely affecting the strength and cutting property.
- In the eighth embodiment of the present invention, a heat treatment, if performed at a temperature of lower than 200°C, may not sufficiently help to remove the inner stress and therefore may not exhibit satisfactory advantages. Accordingly, the treatment temperature should be 200°C or higher. In contrast, a heat treatment, if conducted at a temperature of 350°C or higher, may excessively increase the ductility and lower the strength and cutting property. As used herein the term "cutting property" refers to chip breakability. Chips (scraps) are preferably formed as small or short pieces. This is because long chips become entangled with a working tool (blade) and are rotated therewith, and this damages the surface of the thick plate and breaks the tool. Accordingly, the treatment temperature should be lower than 350°C. A heat treatment performed under above-specified temperature conditions helps to improve the flatness and accuracy of plate thickness without adversely affecting the strength and cutting property.
- A heat treatment, if conducted for a time shorter than one hour, may not sufficiently help intermetallic compounds to be solidly dissolved, and this may often cause the intermetallic compounds to be deposited. Accordingly, the treatment time shouldbe one hour or longer. In contrast, a heat treatment, if conducted for a time of longer than about 8 hours, may be saturated in its effect, and this may cause energy loss. Accordingly, the treatment time is preferably controlled to be 8 hours or shorter.
- The slicing step (S6) is a step of slicing the slab obtained in the heat treatment step (S5) into an aluminum alloy thick plate having a predetermined thickness. The details of this step are as with the slicing step (S5) in the first to fourth embodiments of the present invention.
- The aluminum alloy thick plate produced in the slicing step (S6) may be subjected to a surface smoothing treatment according to necessity in order to remove crystallized substances and oxides formed on the surface of the thick plate or to eliminate gas accumulation in the surface of the thick plate.
- The surface smoothing treatment step (S7) is a step of subjecting the surface of the aluminum alloy thick plate produced in the slicing step (S6) to a surface smoothing treatment. The details of this step are as with the surface smoothing treatment step (S7) in the first to fourth embodiments of the present invention.
- With reference to
Fig. 1 , the methods for manufacturing an aluminum alloy thick plate, according to the ninth to twelfth embodiments of the present invention, each include a melting step (S1), a hydrogen gas removal step (S2), a filtration step (S3), a casting step (S4), a slicing step (S5), and a heat treatment step (S6) in this order. The methods may further include, where necessary, a surface smoothing treatment step (S7) subsequent to the heat treatment step (S6). - In these manufacturing methods, initially, a raw material aluminum alloy is melted in the melting step (S1). Next, hydrogen gas is removed from the molten aluminum alloy in the hydrogen gas removal step (S2), and inclusions such as oxides and non-metals are removed therefrom in the filtration step (S3). Next, the resulting aluminum alloy is cast into a slab in the casting step (S4). The slab is then sliced into an aluminum alloy thick plate having a predetermined thickness in the slicing step (S5). The aluminum alloy thick plate having a predetermined thickness is then subjected to a heat treatment in the heat treatment step (S6) and, where necessary, further subjected to a surface smoothing treatment in the surface smoothing treatment step (S7).
- The manufacturing methods according to the ninth, tenth, eleventh, and twelfth embodiments of the present invention use a 5000 series Al-Mg alloy, a 3000 series Al-Mn alloy, a 6000 series Al-Mg-Si alloy, and a 7000 series Al-Zn-Mg alloy, respectively, as a raw material aluminum alloy. The details of them are as follows.
- A 5000 series Al-Mg alloy as in the first embodiment of the present invention is used in this embodiment. The composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the first embodiment of the present invention.
- A 3000 series Al-Mn alloy as in the second embodiment of the present invention is used in this embodiment. The composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the second embodiment of the present invention.
- A 6000 series Al-Mg-Si alloy as in the third embodiment of the present invention is used in this embodiment. The composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the third embodiment of the present invention.
- A 7000 series Al-Zn-Mg alloy as in the fourth embodiment of the present invention is used in this embodiment. The composition and contents of components of the aluminum alloy, and the reasons why the contents are specified are as in the fourth embodiment of the present invention.
- Next, the respective steps in the manufacturing methods according to the ninth to twelfth embodiments of the present invention will be described below.
- This step is the same as with the melting step (S1) in the first to fourth embodiments of the present invention.
- This step is the same as with the hydrogen gas removal step (S2) in the first to fourth embodiments of the present invention.
- This step is the same as with the filtration step (S3) in the first to fourth embodiments of the present invention.
- This step is the same as with the casting step (S4) in the first to fourth embodiments of the present invention.
- This step is the same as with the slicing step (S5) in the first to fourth embodiments of the present invention.
- The heat treatment step (S6) is a step of carrying out a heat treatment (heat treatment for homogenization) on the aluminum alloy thick plate having a predetermined thickness produced in the slicing step (S5). The heat treatment may be carried out according to a common procedure. Specifically, when the aluminum alloy is a 5000 series Al-Mg alloy (the ninth embodiment of the present invention), a 3000 series Al-Mn alloy (the tenth embodiment of the present invention), anda 6000 seriesAl-Mg-Si alloy (the eleventh embodiment of the present invention), the heat treatment is performed by holding the aluminum alloy thick plate at a temperature of 200°C or higher but lower than 400°C for one hour or longer. When the aluminum alloy is a 7000 series Al-Zn-Mg alloy (the twelfth embodiment of the present invention), the heat treatment is performed by holding the aluminum alloy thick plate at a temperature of 200°C or higher but lower than 350°C for one hour or longer. The details of the other conditions and procedures are as with the heat treatment step (S6) in the first to fourth embodiments of the present invention.
- In the ninth to eleventh embodiments of the present invention, a heat treatment, if conducted at a temperature of lower than 200°C may not sufficiently help to remove the inner stress and therefore may not exhibit satisfactory advantages. Accordingly, the treatment temperature should be 200°C or higher. In contrast, a heat treatment, if conducted at a temperature of 400°C or higher, may excessively increase the ductility and lower the strength and cutting property. As used herein the term "cutting property" refers to chip breakability. Chips (scraps) are preferably formed as small or short pieces. This is because long chips become entangled with a working tool (blade) and are rotated therewith, and this damages the surface of the thick plate and breaks the tool. Accordingly, the treatment temperature should be lower than 400°C. A heat treatment performed under above-specified temperature conditions helps to improve the flatness and accuracy of plate thickness without adversely affecting the strength and cutting property.
- In the twelfth embodiment of the present invention, a heat treatment, if conducted at a temperature of lower than 200°C, may not sufficiently help to remove the inner stress and therefore may not exhibit satisfactory advantages. Accordingly, the treatment temperature should be 200°C or higher. In contrast, a heat treatment, if conducted at a temperature of 350°C or higher, may excessively increase the ductility and lower the strength and cutting property. As used herein the term "cutting property" refers to chip breakability. Chips (scraps) are preferably formed as small or short pieces. This is because long chips become entangled with a working tool (blade) and are rotated therewith, and this damages the surface of the thick plate and breaks the tool. Accordingly, the treatment temperature should be lower than 350°C. A heat treatment performed under above-specified temperature conditions helps to improve the flatness and accuracy of plate thickness without adversely affecting the strength and cutting property.
- A heat treatment, if conducted for a time shorter than one hour, may not sufficiently help intermetallic compounds to be solidly dissolved, and this may often cause the intermetallic compounds to be deposited. Accordingly, the treatment time shouldbe one hour or longer. In contrast, a heat treatment, if conducted for a time of longer than about 8 hours, may be saturated in its effect, and this may cause energy loss. Accordingly, the treatment time is preferably controlled to be 8 hours or shorter.
- This step is the same as with the surface smoothing treatment step (S7) in the first to fourth embodiments of the present invention.
- Next, aluminum alloy thick plates according to the present invention will be described below.
- These aluminum alloy thick plates are manufactured by the procedures of the manufacturing method according to any one of the first to twelfth embodiments of the present invention and have an average crystal grain size of 400 µm or less.
- The aluminum alloy thick plates according to the present invention have an average crystal grain size of 400 µm or less whereby can have improved quality of appearance after anodization and show a smaller within-lot variation.
- A thick plate, if containing intermetallic compounds having large sizes, suffers from unevenness (uneven color) of the cross section and surface of the thick plate upon anodization. The aluminum alloy thick plates according to the present invention, however, contain intermetallic compounds with small sizes and are thereby resistant to such unevenness.
- The measurement of the crystal grain size may be carried out, for example, in the following manner. Specifically, measurements are conducted in cross sections at four points, i.e., at thicknesses of T/5, 2T/5, 3T/5, and 4T/5 ranging from one surface of the slab to the other, wherein T represents the thickness of the slab, and the four measured data are averaged. These measured data are determined typically according to a cutting method. In the cutting method, cross sections of the aluminum alloy thick plate are etched according to a Barker method and are observed with an optical microscope.
- The control of the average crystal grain size to 400 µm or less may be carried out typically in the following manner. Specifically, a cooling rate (average cooling rate from the liquidus temperature to the solidus temperature) during casting is set to be 0.2°C/second or more. Additionally, the aluminum alloy contains 0.1 percent by mass or less of Ti or 0. 3 percent by mass or less of Zr and thereby the crystal grain size can be more finer (smaller) in the manufacturing methods according to the first to third embodiments, the fifth to seventh embodiments, and the ninth to eleventh embodiments of the present invention. The aluminum alloy contains 0.1 percent by mass or less of Ti or 0.25 percent by mass or less of Zr and thereby the crystal grain size can be more finer (smaller) in the manufacturing methods according to the fourth, eighth, and twelfth embodiments of the present invention.
- The resulting aluminum alloy thick plates manufactured by the procedures of the manufacturing methods according to the first to twelfth embodiments of the present invention are satisfactory in the surface condition, flatness, and accuracy of plate thickness as described above and can be used for various applications including semiconductor-related devices such as base substrates, transport devices, and vacuum chambers; electrical and electronic parts and their manufacturing devices; household articles; and mechanical parts. Additionally, they can be recycled and used for other applications.
- There is not need of considering about the corrosion resistance of the aluminum alloy thick plates. This is because thick plates for base substrates and for transport devices are used in clean rooms, they are thereby not required to have generic corrosion resistance. Even when the thick plates are used for vacuum chambers, high corrosion resistance is unnecessary since the environment hardly causes the thick plate to be exposed to a corrosive gas.
- Preferred embodiments have been illustrated above, but the present invention is not limited to these embodiments.
- Some Examples (Experimental Examples) of the present invention will be illustrated below.
- This experimental example relates to the first embodiment of the present invention. The experimental example used 5000 series Al-Mg alloys as the aluminum alloys.
- With reference to Table 1, Alloys 1A to 12A were used as example alloys; while Alloys 13A to 22A were used as comparative example alloys.
-
[Table 1] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Alloy 1A 2.4 0.1 0.3 - - - - 0.01 - 5000 series Alloy 2A 2.4 0.1 0.3 - 0.3 - - 0.01 - 5000 series Alloy 3A 5.0 0.1 0.3 - - - - 0.01 - 5000 series Alloy 4A 8.0 0.1 0.3 - - - - 0.01 0.1 5000 series Alloy 5A 11.0 0.1 0.3 - - - - 0.01 - 5000 series Example Alloy Alloy 6A 5.0 0.3 0.5 0.3 - - - 0.01 - 5000 series Alloy 7A 5.0 0.1 0.3 - 0.05 - - 0.01 - 5000 series Alloy 8A 5.0 0.1 0.3 - - 0.05 - 0.01 - 5000 series Alloy 9A 5.0 0.1 0.3 - 0.7 0.3 - 0.01 0.1 5000 series Alloy 10A 5.0 0.1 0.3 - 0.05 - 0.3 0.01 - 5000 series Alloy 11A 2.5 0.1 0.3 - - 0.15 - 0.01 - 5000 series JIS 5052 alloy Alloy 12A 4.6 0.1 0.2 - 0.6 - - 0.01 - 5000 series JIS 5083 alloy Alloy 13A 1.2 0.1 0.3 - - - - 0.01 - 5000 series Mg content less than lower limit Alloy 14A 14.0 0.1 0.3 - - - - 0.01 - 5000 series Mg content more than upper limit Alloy 15A 5.0 0.8 0.3 - - - - 0.01 - 5000 series Si content more than upper limit Alloy 16A 5.0 0.1 1.0 - - - - 0.01 - 5000 series Fe content more than upper limit Comparative Example Alloy Alloy 17A 5.0 0.1 0.3 0.7 - - - 0.01 - 5000 series Cu content more than upper limit Alloy 18A 5.0 0.1 0.3 - 1.2 - - 0.01 - 5000 series Mn content more than upper limit Alloy 19A 5.0 0.1 0.3 - - 0.6 - 0.01 - 5000 series Cr content more than upper limit Alloy 20A 5.0 0.1 0.3 - - - 0.5 0.01 - 5000 series Zn content more than upper limit Alloy 21A 5.0 0.1 0.3 - - - - 0.15 - 5000 series Ti content more than upper limit Alloy 22A 5.0 0.1 0.3 - - - - 0.01 0.4 5000 series Zr content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 1A to 22A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, sliced samples and hot-rolled samples were prepared from the slabs. The sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
Next, the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 500°C for 4 hours - Accordingly, the resulting sliced samples are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the first embodiment of the present invention, but the resulting hot-rolled samples are not. Among them, only the sliced samples using Alloys 1A to 22A correspond to examples according to the first embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments. were tested for their properties as below.
- In the flatness evaluation, the sliced samples were tested to determine their amounts of warpage (flatness) per 1 m in the casting direction, while the hot-rolled samples were tested to determine their amounts of warpage (flatness) per 1 m in the rolling direction. Samples having an amount of warpage of 0.4 mm or less per 1 m length were evaluated as having accepted flatness (Accepted), while those having an amount of warpage of more than 0.4 mm per 1 m length were evaluated as having unaccepted flatness (Failed).
- In the evaluation of accuracy of plate thickness, thicknesses at six positions of each sample were measured with a micrometer. The six positions are the four corners of the sample thickplate, and two positions each located at a half the length of the long sides and 20 mm inside in the width direction of the thick plate. Samples having thicknesses of 19.94 mm or more and 20.06 mm or less at all the six positions were evaluated as having excellent accuracy of plate thickness (Excellent); and those having thicknesses of 19.90 mm or more and 20.10 mm or less at all the six positions were evaluated as having accepted accuracy of plate thickness (Accepted).
- The strength test was conducted in the following manner. Specifically, JIS No. 5 test pieces were prepared from the aluminum alloy thick plates to perform tensile test thereon, and their tensile strength and 0.2%-proof stress were measured. Samples having a tensile strength of 180 N/mm2 or more were evaluated as having accepted strength (Accepted) ; while those having a tensile strength of less than 180 N/mm2 were evaluated as having unaccepted strength (Failed).
- The anodiz ability evaluation was carried out in the following manner. Anodized aluminum films having a thickness of 10 µm were formed on surface and cross sections of the aluminum alloy thick plates by sulfuric acid anodization under conditions of 15% sulfuric acid, 20°C, and a current density of 2 A/dm2. The appearances of surfaces and cross sections of the thick plates were observed. Samples showing no unevenness (uneven color) in their appearances were evaluated as having accepted anodizability (Accepted); while those showing unevenness in their appearances were evaluated as having unaccepted anodizability (Failed).
- Since the anodizability is affected by the crystal grain sizes of the thick plates, the average crystal grain sizes of the thick plates were determined. The measurements of the average crystal grain sizes were carried out in the following manner. Specifically, measurements were conducted in cross sections at four points, i.e., at thicknesses of T/5, 2T/5, 3T/5, and 4T/5 ranging from one surface of the slab to the other, wherein T represents the thickness of the slab, and the four measured data were averaged. These measured data were determined according to the cutting method. In the cutting method, cross sections of the aluminum alloy thick plate were etched according to the Barker method and were observed with an optical microscope.
- The test results are shown in Tables 2 and 3.
-
[Table 2] Category Number Flatness Accuracy of plate thickness Strength Appearance after anodization Cross section structure (mm/m) Evaluation Evaluation Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Average crystal grain size
(µm)Example Alloy 1A 0.16 Accepted Excellent 196 91 Accepted Accepted Accepted 180 Alloy 2A 0.16 Accepted Excellent 205 100 Accepted Accepted Accepted 180 Alloy 3A 0.19 Accepted Excellent 290 137 Accepted Accepted Accepted 170 Alloy 4A 0.20 Accepted Excellent 316 161 Accepted Accepted Accepted 160 Alloy 5A 0.22 Accepted Excellent 368 175 Accepted Accepted Accepted 140 Alloy 6A 0.20 Accepted Excellent 290 141 Accepted Accepted Accepted 170 Alloy 7A 0.18 Accepted Excellent 287 137 Accepted Accepted Accepted 160 Alloy 8A 0.19 Accepted Excellent 287 139 Accepted Accepted Accepted 160 Alloy 9A 0.20 Accepted Excellent 301 146 Accepted Accepted Accepted 150 Alloy 10A 0.21 Accepted Excellent 285 135 Accepted Accepted Accepted 170 Alloy 11A 0.17 Accepted Excellent 205 102 Accepted Accepted Accepted 170 Sliced Sample Alloy 12A 0.19 Accepted Excellent 288 136 Accepted Accepted Accepted 160 Comparative Example Alloy 13A 0.15 Accepted Excellent 155 62 Failed Accepted Accepted 220 Alloy 14A unproducible due to the generation of casting cracks Alloy 15A 0.20 Accepted Excellent 292 143 Accepted Failed Accepted 160 Alloy 16A 0.20 Accepted Excellent 290 142 Accepted Failed Accepted 150 Alloy 17A 0.21 Accepted Excellent 305 156 Accepted Accepted Accepted 160 Alloy 18A 0.21 Accepted Excellent 308 155 Accepted Failed Accepted 140 Alloy 19A 0.20 Accepted Excellent 305 152 Accepted Failed Accepted 140 Alloy 20A 0.19 Accepted Excellent 287 138 Accepted Accepted Accepted 170 Alloy 21A 0.19 Accepted Excellent 292 142 Accepted Accepted Accepted 140 Alloy 22A 0.19 Accepted Excellent 294 148 Accepted Accepted Accepted 170 -
[Table 3] Category Number Flatness Accuracy of plate thickness Strength Appearance after anodization Cross section structure (mm/m) Evaluation Evaluation Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Average crystal grain size(µm) Alloy 1A 0.41 Failed Excellent 212 105 Accepted Accepted Failed 170 Alloy 2A 0.42 Failed Excellent 221 110 Accepted Accepted Failed 150 Alloy 3A 0.50 Failed Accepted 303 144 Accepted Accepted Failed 160 Alloy 4A 0.61 Failed Accepted 321 168 Accepted Accepted Failed 140 Alloy 5A 0.73 Failed Accepted 388 202 Accepted Accepted Failed 130 Alloy 6A 0.50 Failed Accepted 312 158 Accepted Accepted Failed 160 Alloy 7A 0.50 Failed Accepted 304 155 Accepted Accepted Failed 150 Alloy 8A 0.50 Failed Accepted 309 156 Accepted Accepted Failed 150 Alloy 9A 0.52 Failed Accepted 321 162 Accepted Accepted Failed 140 Alloy 10A 0.50 Failed Accepted 310 150 Accepted Accepted Failed 160 Hot-rolled Sample Comparative Example Alloy 11A 0.43 Failed Excellent 232 133 Accepted Accepted Failed 160 Alloy 12A 0.47 Failed Accepted 312 165 Accepted Accepted Failed 140 Alloy 13A 0.41 Failed Excellent 178 92 Failed Accented Failed 200 Alloy 14A unproducible due to the generation of casting cracks Alloy 15A 0.51 Failed Accepted 305 145 Accepted Failed Failed 170 Alloy 16A 0.52 Failed Accepted 303 144 Accepted Failed Failed 160 Alloy 17A 0.51 Failed Accepted 314 158 Accepted Accepted Failed 150 Alloy 18A 0.52 Failed Accepted 320 157 Accepted Failed Failed 120 Alloy 19A 0.52 Failed Accepted 316 155 Accepted Failed Failed 120 Alloy 20A 0.51 Failed Accepted 300 143 Accepted Accepted Failed 150 Alloy 21A 0.52 Failed Accepted 306 147 Accepted Accepted Failed 160 Alloy 22A 0.51 Failed Accepted 310 154 Accepted Accepted Failed 130 - Table 2 shows the test results of the sliced samples, in which Alloys 1A to 12A correspond to Examples, and Alloys 13A to 22A correspond to comparative examples. Table 3 shows the test results of the hot-rolled samples, in which all Alloys 1A to 22A correspond to comparative examples.
- With reference to Table 2, the samples using Alloys 1A to 13A and 15A to 22A had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
The sample using Alloy 14A contained Mg in a content of more than its upper limit in the material aluminum alloy, thereby suffered from casting cracks, and was unproducible. The sample using Alloy 13A contained Mg in a content of less than its lower limit in the material aluminum alloy and thereby had insufficient strength.
The samples using Alloys 1A to 13A, 17A, and 20A to 22A did not suffer fromunevenness in their appearances of surfaces after anodization. The samples using Alloys 15A, 16A, 18A, and 19A contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, thereby caused a coarse intermetallic compound, and suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 1A to 13A and 15A to 22A did not suffer from unevenness in their appearances of cross sections after anodization.
The samples using Alloys 17A, 20A, 21A, and 22A contained Cu, Zn, Ti, and Zr, respectively, in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were thereby saturated, resulting in inferior economical efficiency. - As is demonstrated in Table 3, the samples using Alloys 1A to 13A and 15A to 22A had accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them showed somewhat inferior accuracy of plate thickness to the sliced samples.
The sample using Alloy 14A contained Mg in a content of more than the upper limit in the material aluminum alloy, suffered from casting cracks, and was unproducible. The sample using Alloy 13A contained Mg in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
The samples using Alloys 15A, 16A, 18A, and 19A contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 1A to 13A and 15A to 22A suffered from unevenness in their appearances of cross sections after anodization. - This experimental example relates to the first embodiment of the present invention. The experimental example used Alloy 3A in Table 1.
- Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloy 3A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, the slabs were further subjected to a slicing step to give sliced samples. The sliced samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
The sliced samples were then subjected to a heat treatment step. Specifically, the sliced samples were further subjected to a heat treatment under conditions given in Table 4. -
[Table 4] Category Number Heat treatment for uniformization Flatness Accuracy of plate thickness (mm/m) Evaluation Evaluation Sliced Sample Example A1 Alloy 3A 420°C for2 hr 0.21 Excellent Excellent A2 Alloy 3A 500°C for4 hr 0.19 Excellent Excellent Comparative Example A3 Alloy 3A none 0.30 Accepted Accepted A4 Alloy 3A 380°C for 4 hr 0.26 Accepted Excellent A5 Alloy 3A 530°C for 2 hr unproducible due to the generation of burning - Samples A1 and A2, whose heat treatment conditions satisfy the conditions according to the first embodiment of the present invention, correspond to examples according to the first embodiment of the present invention; whereas Samples A3 to A5, whose heat treatment conditions do not satisfy the conditions according to the first embodiment of the present invention, correspond to comparative examples.
- Next, the sliced samples after the treatments were subjected to a flatness evaluation test and an evaluation test for accuracy of plate thickness.
- In the flatness evaluation, the samples were tested to determine their amounts of warpage (flatness) per 1 m in the casting direction. Samples having an amount of warpage of 0.4 mm or less per 1 m length were evaluated as having accepted flatness (Accepted), and those having an amount of warpage of 0.25 mm or less per 1 m length were evaluated as having excellent flatness (Excellent).
- The evaluation test for accuracy of plate thickness is as in First Experimental Example.
- The test results are shown in Table 4.
- As is demonstrated in Table 4, ExamplesAl andA2, whoseheat treatment conditions satisfy the conditions specified in the first embodiment of the present invention, excelled in flatness and accuracy of plate thickness. Comparative Example A3 did not undergo a heat treatment and was thereby somewhat inferior in flatness and accuracy of plate thickness to Examples A1 and A2. Comparative Example A4 underwent a heat treatment at a temperature lower than the temperature range specified in the first embodiment of the present invention (lower than 400°C) and was thereby somewhat inferior in flatness to Examples A1 andA2. Comparative Example A5 underwent a heat treatment at a temperature higher than the temperature range specified in the first embodiment of the present invention (higher than the melting point), whereby suffered from internal partial melting and resulting internal defects, and was unproducible.
- This experimental example relates to the second embodiment of the present invention. The experimental example used 3000 series Al-Mn alloys as the aluminum alloys.
- With reference to Table 5, Alloys 23A and 24A were used as example alloys; while Alloys 25A and 26A were used as comparative example alloys.
-
[Table 5] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy 23A - 0.1 0.3 - 0.5 - - 0.01 - 3000 series Alloy 24A - 0.1 0.4 - 0.9 - - 0.01 - 3000 series Comparative Example Alloy Alloy 25A - 0.1 0.4 - 0.2 - - 0.01 - 3000 series Mn content less than lower limit Alloy 26A - 0.1 0.3 - 1.7 - - 0.01 - 3000 series Mn content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 23A to 26A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, sliced samples and hot-rolled samples were prepared from the slabs. The sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
Next, the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 500°C for 4 hours. - Accordingly, the sliced samples after the treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the second embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 23A and 24A correspond to examples according to the second embodiment of the present invention.
- Next, the prepared sliced samples and hot-rolled samples were further subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, a strength test, and an anodizability evaluation test.
- The procedures and criteria of the respective tests are as in First Experimental Example.
However, the properties of thick plates vary depending on the type of alloy used, and the criteria for the strength were modified as follows. Specifically, samples having a tensile strength of 90 N/mm2 or more were evaluated as having accepted strength (Accepted), whereas those having a tensile strength of less than 90 N/mm2 were evaluated as having unaccepted strength (Failed). - The test results are shown in Table 6.
-
[Table 6] Category Number Flatness Accuracy of plate thickness Strength Appearance after anodization (mm/m) Evaluation Evaluation Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Sliced Sample Example Alloy 23A 0.19 Accepted Excellent 92 36 Accepted Accepted Accepted Alloy 24A 0.21 Accepted Excellent 99 37 Accepted Accepted Accepted Comparative Example Alloy 25A 0.19 Accepted Excellent 82 36 Failed Accepted Accepted Alloy 26A 0.24 Accepted Excellent 114 52 Accepted Failed Accepted Hot-rolled Sample Comparative Example Alloy 23A 0.41 Failed Excellent 112 54 Accepted Accepted Failed Alloy 24A 0.42 Failed Accepted 116 57 Accepted Accepted Failed Alloy 25A 0.41 Failed Excellent 98 50 Accepted Accepted Failed Alloy 26A 0.45 Failed Accepted 138 70 Accepted Failed Failed - As is demonstrated in Table 6, the samples using Alloys 23A to 26A had small processing strain and showed little warpage, i.e., they had satisfactoryflatness. Additionally, theyexcelledin accuracy of plate thickness.
The sample using Alloy 25A contained Mn in a content less than the lower limit in the material aluminum alloy and thereby had insufficient strength. The sample using Alloy 26A contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization. The samples using Alloys 23A to 26A did not suffer from unevenness in their appearances of cross sections after anodization. - As is demonstrated in Table 6, the samples using Alloy 23A to 26A suffered from accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them were somewhat inferior in accuracy of plate thickness to the corresponding sliced samples.
The sample using Alloy 25A contained Mn in a content of less than the lower limit in the material aluminum alloy and was thereby somewhat inferior in strength to the other hot-rolled samples. The sample using Alloy 26A contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization. The samples using Alloy 23A to 26A suffered from unevenness in their appearances of cross sections after anodization. - This experimental example relates to the third embodiment of the present invention. The experimental example used 6000 series Al-Mg-Si alloys as the aluminum alloys.
- With reference to Table 7, Alloys 27A and 28A were used as example alloys; while Alloys 29A to 32A were used as comparative example alloys.
-
[Table 7] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy 27A 1.0 0.5 0.5 0.3 0.1 0.2 0.2 0.02 - 6000 series Alloy 28A 0.5 1.0 0.2 - 0.1 - - 0.02 - 6000 series Comparative Example Alloy Alloy 29A 0.9 0.1 0.5 - 0.1 - - 0.02 - 6000 series Si content less than lower limit Alloy 30A 0.9 1.8 0.4 - 0.1 - - 0.02 - 6000 series Si content more than upper limit Alloy 31A 0.2 0.5 0.5 - 0.1 - - 0.02 - 6000 series Mg content less than lower limit Alloy 32A 1.7 0.5 0.4 - 0.1 - - 0.02 - 6000 series Mg content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloy 27A to 32A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, sliced samples and hot-rolled samples were prepared from the slabs. The sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
Next, the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 500°C for 4 hours.
The resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 520°C and subsequently to an aging treatment at 175°C for 8 hours. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the third embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 27A and 28A correspond to examples according to the third embodiment of the present invention.
- Next, the sliced samples andhot-rolled samples after the treatments were subjected to a strength test and an anodizability evaluation test.
- The procedures and criteria of the respective tests are as in First Experimental Example.
However, the properties of thick plates vary depending on the type of alloy used, and the criteria for the strength were modified as follows. Specifically, samples having a tensile strength of 200 N/mm2 or more were evaluated as having accepted strength (Accepted), whereas those having a tensile strength of less than 200 N/mm2 were evaluated as having unaccepted strength (Failed). - The test results are shown in Table 8.
-
[Table 8] Category Number Strength Appearance after anodization Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Sliced Sample Example Alloy 27A 322 272 Accepted Accepted Accepted Alloy 28A 296 250 Accepted Accepted Accepted Comparative Example Alloy 29A 114 67 Failed Accepted Accepted Alloy 30A 342 302 Accepted Failed Accepted Alloy 31A 178 125 Failed Accepted Accepted Alloy 32A 210 124 Accepted Accepted Accepted Hot-rolled Sample Comparative Example Alloy 27A 346 276 Accepted Accepted Failed Alloy 28A 318 276 Accepted Accepted Failed Alloy 29A 138 88 Failed Accepted Failed Alloy 30A 365 323 Accepted Failed Failed Alloy 31A 197 143 Failed Accepted Failed Alloy 32A 235 146 Accepted Accepted Failed - As is demonstrated in Table 8, the samples using Alloys 29A and 31A contained Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength. The sample using Alloy 30A contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization. The sample using Alloy 32A contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency. The samples using Alloys 27A to 32A did not suffer fromunevenness in their appearances of cross sections after anodization.
- As is demonstrated in Table 8, the samples using Alloys 29A and 31A contained Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength. The sample using Alloy 30A contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization. The sample using Alloy 32A contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency. The samples using Alloy 27A to 32A suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the fourth embodiment of the present invention. The experimental example used 7000 series Al-Zn-Mg alloys as the aluminum alloys.
- With reference to Table 9, Alloys 33A and 34A were used as example alloys, while Alloys 35A to 38A were used as comparative example alloys.
-
[Table 9] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy 33A 2.5 0.1 0.2 1.8 - 0.2 5.5 0.02 - 7000 series Alloy 34A 3.5 0.2 0.2 2.0 - - 8.5 0.02 0.2 7000 series Comparative Example Alloy Alloy 35A 0.3 0.1 0.2 2.2 - 0.1 4.0 0.02 - 7000 series Mg content less than lower limit Alloy 36A 5.0 0.2 0.2 2.0 - 0.1 5.0 0.02 - 7000 series Mg content more than upper limit Alloy 37A 2.5 0.1 0.2 2.2 - 0.1 2.4 0.02 - 7000 series Zn content less than lower limit Alloy 38A 3.0 0.2 0.2 2.0 - 0.1 9.5 0.02 - 7000 series Zn content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 33A to 38A to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, sliced samples and hot-rolled samples were prepared from the slabs. The sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
Next, the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 500°C for 4 hours.
The resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 470°C and subsequently to an aging treatment at 120°C for 48 hours. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the fourth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 33A and 34A correspond to examples according to the fourth embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments were subjected to a strength test and an anodizability evaluation test.
- The procedures and criteria of the respective tests are as in First Experimental Example.
However, the properties of thick plates vary depending on the type of alloy used, and the criteria for the strength were modified as follows. Specifically, samples having a tensile strength of 250 N/mm2 or more were evaluated as having accepted strength (Accepted), whereas those having a tensile strength of less than 250 N/mm2 were evaluated as having unaccepted strength (Failed). - The test results are shown in Table 10.
-
[Table 10] Category Number Strength Appearance after anodization Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Sliced Sample Example Alloy 33A 425 364 Accepted Accepted Accepted Alloy 34A 513 450 Accepted Accepted Accepted Comparative Example Alloy 35A 198 167 Failed Accepted Accepted Alloy 36A 289 189 Accepted Failed Accepted Alloy 37A 210 132 Failed Accepted Accepted Alloy 38A 605 526 Accepted Failed Accepted Hot-rolled Sample Comparative Example Alloy 33A 442 380 Accepted Accepted Failed Alloy 34A 535 474 Accepted Accepted Failed Alloy 35A 212 174 Failed Accepted Failed Alloy 36A 305 203 Accepted Failed Failed Alloy 37A 227 148 Failed Accepted Failed Alloy 38A 616 536 Accepted Failed Failed - As is demonstrated in Table 10, the samples using Alloys 35A and 37A contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength. The samples using Alloys 36A and 38A contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 33A to 38A did not suffer from unevenness in their appearances of cross sections after anodization.
- As is demonstrated in Table 10, the samples using Alloys 35A and 37A contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength. The samples using Alloys 36A and 38A contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 33A to 38A suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the fifth embodiment of the present invention. The experimental example used 5000 series Al-Mg alloys as the aluminum alloys.
- With reference to Table 11, Alloys 1B to 12B were used as example alloys; while Alloys 13B to 22B were used as comparative example alloys.
-
[Table 11] Category Number Element (percent by mass) Alloy type Remarks Mg si Fe Cu Mn Cr Zn Ti Zr Alloy 1B 2.6 0.1 0.3 - - - - 0.01 - 5000 series Alloy 2B 2.6 0.1 0.3 - 0.3 - - 0.01 - 5000 series Alloy 3B 4.5 0.1 0.3 - - - - 0.01 - 5000 series Alloy 4B 7.5 0.1 0.3 - - - - 0.01 0.1 5000 series Alloy 5B 10.5 0.1 0.3 - - - - 0.01 - 5000 series Alloy 6B 4.5 0.3 0.5 0.3 - - - 0.01 - 5000 series Example Alloy Alloy 7B 4.5 0.1 0.3 - 0.05 - - 0.01 - 5000 series Alloy 8B 4.5 0.1 0.3 - - 0.05 - 0.01 - 5000 series Alloy 9B 4.5 0.1 0.3 - 0.7 0.3 - 0.01 0.1 5000 series Alloy 10B 4.5 0.1 0.3 - 0.05 - 0.3 0.01 - 5000 series Alloy 11B 2.5 0.1 0.3 - - 0.15 - 0.01 - 5000 series JIS 5052 alloy Alloy 12B 4.6 0.1 0.2 - 0.6 - - 0.01 - 5000 series JIS 5083 alloy Alloy 13B 1.3 0.1 0.3 - - - - 0.01 - 5000 series Mg content less than lower limit Alloy 14B 13.5 0.1 0.3 - - - - 0.01 - 5000 series Mg content more than upper limit Alloy 15B 4.5 0.8 0.3 - - - - 0.01 - 5000 series Si content more than upper limit Alloy 16B 4.5 0.1 1.0 - - - - 0.01 - 5000 series Fe content more than upper limit Comparative Example Alloy Alloy 17B 4.5 0.1 0.3 0.7 - - - 0.01 - 5000 series Cu content more than upper limit Alloy 18B 4.5 0.1 0.3 - 1.2 - - 0.01 - 5000 series Mn content more than upper limit Alloy 19B 4.5 0.1 0.3 - - 0.6 - 0.01 - 5000 series Cr content more than upper limit Alloy 20B 4.5 0.1 0.3 - - - 0.5 0.01 - 5000 series Zn content more than limit Alloy 21B 4.5 0.1 0.3 - - - - 0.15 - 5000 series upper Ti content than limit Alloy 22B 4.5 0.1 0.3 - - - - 0.01 0.4 5000 series more upper Zr content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 1B to 22B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, the slabs were further subjected to a treatment in a heat treatment step, in which they were held at a temperature of 350°C for 4 hours.
Next, sliced samples and hot-rolled samples were prepared from the thermally treated slabs. The sliced samples were prepared by slicing the slabs in a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the fifth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 1B to 22B correspond to examples according to the fifth embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments were subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, a strength test, and an anodizability evaluation test. The procedures and criteria of the respective tests are as in First Experimental Example.
- The test results are shown in Tables 12 and 13.
-
[Table 12] Category Number Flatness Accuracy of plate thickness Strength Appearance after anodization Cross section structure (mm/m) Evaluation Evaluation Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Average crystal grain size (µm) Example Alloy 1B 0.25 Accepted Excellent 214 100 Accepted Accepted Accepted 170 Alloy 2B 0.25 Accepted Excellent 225 108 Accepted Accepted Accepted 170 Alloy 3B 0.28 Accepted Excellent 308 146 Accepted Accepted Accepted 170 Alloy 48 0.28 Accepted Excellent 335 172 Accepted Accepted Accepted 150 Alloy 5B 0.31 Accepted Excellent 387 187 Accepted Accepted Accepted 140 Alloy 6B 0.29 Accepted Excellent 311 140 Accepted Accepted Accepted 160 Alloy 7B 0.26 Accepted Excellent 307 147 Accepted Accepted Accepted 150 Alloy 8B 0.27 Accepted Excellent 316 147 Accepted Accepted Accepted 150 Alloy 9B 0.28 Accepted Excellent 320 156 Accepted Accepted Accepted 150 Alloy 10B 0.29 Accepted Excellent 305 146 Accepted Accepted Accepted 160 Alloy 11B 0.26 Accepted Excellent 226 110 Accepted Accepted Accepted 160 Sliced Sample Alloy 12B 0.28 Accepted Excellent 309 146 Accepted Accepted Accepted 150 Comparative Example Alloy 13B 0.25 Accepted Excellent 175 72 Failed Accepted Accepted 210 Alloy 14B unproducible due to the generation of casting cracks Alloy 15B 0.29 Accepted Excellent 310 152 Accepted Failed Accepted 160 Alloy 16B 0.30 Accepted Excellent 309 152 Accepted Failed Accepted 150 Alloy 17B 0.29 Accepted Excellent 324 167 Accepted Accepted Accepted 150 Alloy 18B 0.30 Accepted Excellent 328 165 Accepted Failed Accepted 130 Alloy 19B 0.29 Accepted Excellent 327 161 Accepted Failed Accepted 140 Alloy 20B 0.28 Accepted Excellent 308 149 Accepted Accepted Accepted 160 Alloy 21B 0.29 Accepted Excellent 315 150 Accepted Accepted Accepted 130 Alloy 22B 0.28 Accepted Excellent 316 157 Accepted Accepted Accepted 160 -
[Table 13] Category Number Flatness Accuracy of plate thickness Strength Appearance after anodization Cross section structure (mm/m) Evaluation Evaluation Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Average crystal grain size (µm) Alloy 1B 0.42 Failed Excellent 215 103 Accepted Accepted Failed 160 Alloy 2B 0.43 Failed Excellent 224 108 Accepted Accepted Failed 150 Alloy 3B 0.48 Failed Accepted 293 139 Accepted Accepted Failed 170 Alloy 4B 0.60 Failed Accepted 312 162 Accepted Accepted Failed 140 Alloy 5B 0.71 Failed Accepted 379 197 Accepted Accepted Failed 140 Alloy 6B 0.48 Failed Excellent 302 154 Accepted Accepted Failed 160 Alloy 7B 0.49 Failed Accepted 295 150 Accepted Accepted Failed 160 Alloy 8B 0.48 Failed Accepted 298 151 Accepted Accepted Failed 150 Alloy 9B 0.51 Failed Accepted 310 157 Accepted Accepted Failed 150 Alloy 10B 0.49 Failed Accepted 299 145 Accepted Accepted Failed 160 Alloy 11B 0.42 Failed Excellent 222 126 Accepted Accepted Failed 170 Hot-rolled Sample Comparative Example Alloy 12B 0.49 Failed Accepted 303 160 Accepted Accepted Failed 150 Alloy 13B 0.41 Failed Excellent 179 95 Failed Accented Failed 210 Alloy 14B unproducible due to the generation of casting cracks Alloy 15B 0.49 Failed Excellent 295 139 Accepted Failed Failed 170 Alloy 16B 0.50 Failed Accepted 294 139 Accepted Failed Failed 170 Alloy 17B 0.49 Failed Accepted 302 154 Accepted Accepted Failed 160 Alloy 18B 0.49 Failed Excellent 309 153 Accepted Failed Failed 130 Alloy 19B 0.48 Failed Accepted 306 150 Accepted Failed Failed 120 Alloy 20B 0.49 Failed Accepted 290 139 Accepted Accepted Failed 160 Alloy 21B 0.50 Failed Accepted 296 142 Accepted Accepted Failed 160 Alloy 22B 0.49 Failed Accepted 299 150 Accepted Accepted Failed 140 - Table 12 shows the test results of the sliced samples. In Table 12, the samples using Alloys 1B to 12B correspond to examples according to the fifth embodiment of the present invention, whereas the samples using Alloys 13B to 22B correspond to comparative examples. Table 13 shows the test results of the hot-rolled samples. In Table 13, all the samples using Alloys 1B to 22B correspond to comparative examples.
- As is demonstrated in Table 12, the samples using Alloys 1B to 13B and 15B to 22B had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
The sample using Alloy 14B contained Mg in a content of more than the upper limit in the material aluminum alloy, thereby suffered from casting cracks, and was unproducible. The sample using Alloy 13B contained Mg in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
The samples using Alloys 1B to 13B, 17B, and 20B to 22B did not suffer from unevenness in their appearances of surfaces after anodization. The samples using Alloys 15B, 16B, 18B, and 19B contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 1B to 13B and 15B to 22B did not suffer from unevenness in their appearances of cross sections after anodization.
The samples using Alloys 17B, 20B, 21B, and 22B contained Cu, Zn, Ti, and Zr, respectively, in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency. - As is demonstrated in Table 13, the samples using Alloys 1B to 13B and 15B to 22B suffered from accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them were somewhat inferior in accuracy of plate thickness to the corresponding sliced samples.
The sample using Alloy 14B contained Mg in a content of more than the upper limit in the material aluminum alloy, suffered from casting cracks, and was unproducible. The sample using Alloy 13B contained Mg in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
The samples using Alloys 15B, 16B, 18B, and 19B contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 1B to 13B and 15B to 22B suffered from unevenness in their appearances of cross sections after anodization. - This experimental example relates to the fifth embodiment of the present invention. The experimental example used Alloy 3B in Table 11.
- Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloy 3B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, the slabs were further subjected to a treatment in a heat treatment step, in which they were further subjected to a heat treatment under conditions given in Table 14.
The thermally treated slabs were sliced in a slicing step to give sliced samples. The sliced samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long. -
[Table 14] Category Number Heat treatment for uniformization Flatness Accuracy of plate thickness Cutting property (mm/m) Evaluation Evaluation (number of chips/10g) Evaluation Sliced Sample Example B1 Alloy 3B 350°C for 2 hr 0.28 Accepted Excellent 1030 Accepted B2 Alloy 3B 250°C for 4 hr 0.36 Accepted Excellent 1140 Accepted Comparative Example B3 Alloy 3B none 0.44 Failed Accepted 1290 Accepted B4 Alloy 3B 420°C for 4 hr 0.26 Accepted Excellent 920 Failed B5 Alloy 3B 150°C for 2 hr 0.42 Failed Accepted 1230 Accepted - Accordingly, Samples B1 and B2, whose heat treatment conditions satisfy the conditions specified in the fifth embodiment of the present invention, correspond to examples according to the fifth embodiment of the present invention; whereas Samples B3 to B5, whose heat treatment conditions do not satisfy the conditions specified in the fifth embodiment of the present invention, correspond to comparative examples.
- The sliced samples after the treatments were subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, and a cutting property evaluation test.
- In the flatness evaluation, the samples were tested to determine their amounts of warpage (flatness) per 1 m in the casting direction. Samples having an amount of warpage of 0.4 mm or less per 1 m length were evaluated as having accepted flatness (Accepted), while those having an amount of warpage of more than 0.4 mm per 1 m length were evaluated as having unaccepted flatness (Failed).
- The evaluation test for accuracy of plate thickness is as in First Experimental Example.
- The evaluation of cutting property, i.e., chip breakability was performed by drilling a sample and measuring the number of chips per unit mass. Specifically, the sample was drilled with a drill having a diameter of 5 mm at a number of revolutions of 7000 rpm and a feed rate of 300 mm/minute, and the number of generated chips per 10 g was measured. Samples having a number of chips of 1000 or more per 10 g were evaluated as having accepted cutting property (Accepted) ; whereas those having a number of chips of less than 1000 per 10 g were evaluated as having unaccepted cutting property (Failed).
- The test results are shown in Table 14.
- As is demonstrated in Table 14, Examples B1 and B2, whose heat treatment conditions satisfy the conditions specified in the fifth embodiment of the present invention, excelled in flatness, accuracy of plate thickness, and cutting property. Comparative Example B3 did not undergo a heat treatment, thereby show poor flatness, and was somewhat inferior in accuracy of plate thickness to Examples B1 and B2. Comparative Example B4, whose heat treatment had been performed at a temperature higher than the range specified in the fifth embodiment of the present invention, was thereby inferior in cutting property. Comparative Example B5, whose heat treatment had been performed at a temperature lower than the range specified in the fifth embodiment of the present invention, thereby showed poor flatness, and was somewhat inferior in accuracy of plate thickness to Examples B1 and B2.
- This experimental example relates to the sixth embodiment of the present invention. The experimental example used 3000 series Al-Mn alloys as the aluminum alloys.
- With reference to Table 15, Alloys 23B and 24B were used as example alloys; while Alloys 25B and 26B were used as comparative example alloys.
-
[Table 15] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy 23B - 0.1 0.3 - 0.5 - - 0.0 1 - 3000 series Alloy 24B - 0.1 0.4 - 0.9 - - 0.0 1 - 3000 series Comparative Example Alloy Alloy 25B - 0.1 0.4 - 0.2 - - 0.0 1 - 3000 series Mn content less than lower limit Alloy 26B - 0.1 0.3 - 1.7 - - 0.0 1 - 3000 series Mn content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 23B to 26B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, the slabs were further subjected to a treatment in a heat treatment step, in which they were held at a temperature of 350°C for 4 hours.
Next, sliced samples and hot-rolled samples were prepared from the thermally treated slabs. The sliced samples were prepared by slicing the slabs in a slicing step, while the hot-rolled samples were prepared by subj ecting the slabs to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the sixth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 23B and 24B correspond to examples according to the sixth embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments were subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, a strength test, and an anodizability evaluation test.
- The procedures and criteria of the respective tests are as in First Experimental Example.
However, the properties of thick plates vary depending on the type of alloy used, and the criteria for the strength were modified as follows. Specifically, samples having a tensile strength of 90 N/mm2 or more were evaluated as having accepted strength (Accepted); whereas those having a tensile strength of less than 90 N/mm2 were evaluated as having unaccepted strength (Failed). - The test results are shown in Table 16.
-
[Table 16] Category Number Flatness Accuracy of plate thickness Strength Appearance after anodization (mm/m) Evaluation Evaluation Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Sliced Sample Example Alloy 23B 0.23 Accepted Excellent 95 38 Accepted Accepted Accepted Alloy 24B 0.23 Accepted Excellent 101 39 Accepted Accepted Accepted Comparative Example Alloy 25B 0.22 Accepted Excellent 85 38 Failed Accepted Accepted Alloy 26B 0.24 Accepted Excellent 118 50 Accepted Failed Accepted Hot-rolled Sample Comparative Example Alloy 23B 0.41 Failed Excellent 113 54 Accepted Accepted Failed Alloy 24B 0.41 Failed Accepted 116 56 Accepted Accepted Failed Alloy 25B 0.41 Failed Excellent 97 49 Accepted Accepted Failed Alloy 26B 0.44 Failed Accepted 140 71 Accepted Failed Failed - As is demonstrated in Table 16, the samples using Alloys 23B to 26B had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
The sample using Alloy 25B contained Mn in a content less than the lower limit in the material aluminum alloy and thereby had insufficient strength. The sample using Alloy 26B contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization. The samples using Alloys 23B to 26B did not suffer from unevenness in their appearances of cross sections after anodization. - With reference to Table 16, the samples using Alloys 23B to 26B suffered from accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them were somewhat inferior in accuracy of plate thickness to the corresponding sliced samples.
The sample using Alloy 25B contained Mn in a content of less than the lower limit in the material aluminum alloy and was thereby somewhat inferior in strength to the other hot-rolled samples. The sample using Alloy 26B contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization. The samples using Alloys 23B to 26B suffered from unevenness in their appearances of cross sections after anodization. - This experimental example relates to the seventh embodiment of the present invention. The experimental example used 6000 series Al-Mg-Si alloys as the aluminum alloys.
- With reference to Table 17, Alloys 27B and 28B were used as example alloys; while Alloys 29B to 32B were used as comparative example alloys.
-
[Table 17] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy 27B 0.9 0.5 0.5 0.3 0.1 0.2 0.2 0.02 - 6000 series Alloy 28B 0.5 0.9 0.2 - 0.1 - - 0.02 - 6000 series Comparative Example Alloy Alloy 29B 0.9 0.1 0.5 - 0.1 - - 0.02 - 6000 series Si content less than lower limit Alloy 30B 0.9 1.8 0.4 - 0.1 - - 0.02 - 6000 series Si content more than upper limit Alloy 31B 0.2 0.5 0.5 - 0.1 - - 0.02 - 6000 series Mg content less than lower limit Alloy 32B 1.7 0.5 0.4 - 0.1 - - 0.02 - 6000 series Mg content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 27B to 32B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, the slabs were further subjected to a treatment in a heat treatment step, in which they were held at a temperature of 350°C for 4 hours.
Next, sliced samples and hot-rolled samples were prepared from the thermally treated slabs. The sliced samples were prepared by slicing the slabs in a slicing step, while the hot-rolled samples were prepared by subj ecting the slabs to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
The resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 520°C and subsequently to an aging treatment at 175°C for 8 hours. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the seventh embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 27B and 28B correspond to examples according to the seventh embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments were subjected to a strength test and an anodizability evaluation test.
- The procedures and criteria of the respective tests are as in First Experimental Example.
However, the properties of thick plates vary depending on the type of alloy used, and the criteria for the strength were modified as follows. Specifically, samples having a tensile strength of 200 N/mm2 or more were evaluated as having accepted strength (Accepted) ; while those having a tensile strength of less than 200 N/mm2 were evaluated as having unaccepted strength (Failed). - The test results are shown in Table 18.
-
[Table 18] Category Number Strength Appearance after anodization Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Sliced Sample Example Alloy 27B 320 272 Accepted Accepted Accepted Alloy 28B 295 251 Accepted Accepted Accepted Comparative Example Alloy 29B 112 65 Failed Accepted Accepted Alloy 30B 339 300 Accepted Failed Accepted Alloy 31B 175 122 Failed Accepted Accepted Alloy 32B 212 126 Accepted Accepted Accepted Hot-rolled Sample Comparative Example Alloy 27B 346 273 Accepted Accepted Failed Alloy 28B 319 274 Accepted Accepted Failed Alloy 29B 135 86 Failed Accepted Failed Alloy 30B 362 322 Accepted Failed Failed Alloy 31B 198 143 Failed Accepted Failed Alloy 32B 233 145 Accepted Accepted Failed - As is demonstrated in Table 18, the samples using Alloys 29B and 31B contained Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength. The sample using Alloy 30B contained Si in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization. The sample using Alloy 32B contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency. The samples using Alloys 27B to 32B did not suffer from unevenness in their appearances of cross sections after anodization.
- As is demonstrated in Table 18, the samples using Alloys 29B and 31B contained Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength. The sample using Alloy 30B contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surfaces after anodization. The sample using Alloy 32B contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency. The samples using Alloys 27B to 32B suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the eighth embodiment of the present invention. The experimental example used 7000 series Al-Zn-Mg alloys as the aluminum alloys.
- With reference to Table 19, Alloys 33B and 34B were used as example alloys; while Alloys 35B to 38B were used as comparative example alloys.
-
[Table 19] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy 33B 2.5 0.1 0.2 1.8 - 0.2 4.0 0.0 2 - 7000 series Alloy 34B 3.5 0.2 0.2 2.0 - - 8.0 0.0 2 0.2 7000 series Comparative Example Alloy Alloy 35B 0.3 0.1 0.2 2.2 - 0.1 4.0 0.0 2 - 7000 series Mg content less than lower limit Alloy 36B 5.0 0.2 0.2 2.0 - 0.1 5.0 0.0 2 - 7000 series Mg content more than upper limit Alloy 37B 2.5 0.1 0.2 2.2 - 0.1 2.4 0.0 2 - 7000 series Zn content less than lower limit Alloy 38B 3.0 0.2 0.2 2.0 - 0.1 9.5 0.0 2 - 7000 series Zn content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 33B to 38B to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, the slabs were further subjected to a treatment in a heat treatment step, in which they were held at a temperature of 300°C for 4 hours.
Next, sliced samples and hot-rolled samples were prepared from the thermally treated slabs. The sliced samples were prepared by slicing the slabs in a slicing step, while the hot-rolled samples were prepared by subj ecting the slabs to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
The resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 470°C and subsequently to an aging treatment at 120°C for 48 hours. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the eighth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 33B and 34B correspond to examples according to the eighth embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments were subjected to a strength test and an anodizability evaluation test.
- The procedures and criteria of the respective tests are as in First Experimental Example.
However, the properties of thick plates vary depending on the type of alloy used, and the criteria for the strength were modified as follows. Specifically, samples having a tensile strength of 250 N/mm2 or more were evaluated as having accepted strength (Accepted) ; while those having a tensile strength of less than 250 N/mm2 were evaluated as having unaccepted strength (Failed). - The test results are shown in Table 20.
-
[Table 20] Category Number Strength Appearance after anodization Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Sliced Sample Example Alloy 33B 422 363 Accepted Accepted Accepted Alloy 34B 510 449 Accepted Accepted Accepted Comparative Example Alloy 35B 193 165 Failed Accepted Accepted Alloy 36B 287 188 Accepted Failed Accepted Alloy 37B 209 130 Failed Accepted Accepted Alloy 38B 602 525 Accepted Failed Accepted Hot-rolled Sample Comparative Example Alloy 33B 441 380 Accepted Accepted Failed Alloy 34B 533 472 Accepted Accepted Failed Alloy 35B 210 172 Failed Accepted Failed Alloy 36B 303 202 Accepted Failed Failed Alloy 37B 224 146 Failed Accepted Failed Alloy 38B 614 535 Accepted Failed Failed - As is demonstrated in Table 20, the samples using Alloy 35B and 37B contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength. The samples using Alloys 36B and 38B contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 33B to 38B did not suffer from unevenness in their appearances of cross sections after anodization.
- As is demonstrated in Table 20, the samples using Alloys 35B and 37B contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength. The samples using Alloys 36B and 38B contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and thereby suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 33B to 38B suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the ninth embodiment of the present invention. The experimental example used 5000 series Al-Mg alloys as the aluminum alloys.
- With reference to Table 21, Alloys 1C to 12C were used as example alloys; while Alloys 13C to 22C were used as comparative example alloys.
-
[Table 21] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy 1C 2.5 0.1 0.3 - - - - 0.01 - 5000 series Alloy 2C 2.5 0.1 0.3 - 0.3 - - 0.01 - 5000 series Alloy 3C 4.7 0.1 0.3 - - - - 0.01 - 5000 series Alloy 4C 7.5 0.1 0.3 - - - - 0.01 0.1 5000 series Alloy 5C 10.4 0.1 0.3 - - - - 0.01 - 5000 series Alloy 6C 4.7 0.3 0.5 0.3 - - - 0.01 - 5000 series Alloy 7C 4.7 0.1 0.3 - 0.0 5 - - 0.01 - 5000 series Alloy 8C 4.7 0.1 0.3 - - 0.0 5 - 0.01 - 5000 series Alloy 9C 4.7 0.1 0.3 - 0.7 0.3 - 0.01 0.1 5000 series Alloy 10C 4.7 0.1 0.3 - 0.0 5 - 0.3 0.01 - 5000 series Alloy 11C 2.5 0.1 0.3 - - 0.1 5 - 0.01 - 5000 series JIS 5052 alloy Alloy 12C 4.7 0.1 0.2 - 0.6 - - 0.01 - 5000 series JIS 5083 alloy Alloy 13C 1.4 0.1 0.3 - - - - 0.01 - 5000 series Mg content less than lower limit Alloy 14C 13.0 0.1 0.3 - - - - 0.01 - 5000 series Mg content more than upper limit Alloy 15C 4.7 0.8 0.3 - - - - 0.01 - 5000 series Si content more than upper limit Alloy 16C 4.7 0.1 1.0 - - -- - 0.01 - 5000 series Fe content more than upper limit Comparative Example Alloy Alloy 17C 4.7 0.1 0.3 0.7 - - - 0.01 - 5000 series Cu content more than upper limit Alloy 18C 4.7 0.1 0.3 1.2 0.01 5000 series Mn content more than upper limit Alloy 19C 4.7 0.1 0.3 0.6 0.01 5000 series Cr content more than upper limit Alloy 20C 4.7 0.1 0.3 0.5 0.01 5000 series Zn content more than upper limit Alloy 21C 4.7 0.1 0.3 0.15 5000 series Ti content more than upper limit Alloy 22C 4.7 0.1 0.3 0.01 0.4 5000 series Zr content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 1C to 22C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, sliced samples and hot-rolled samples were prepared from the slabs. The sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
Next, the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 350°C for 4 hours. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the ninth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 1C to 22C correspond to examples according to the ninth embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments were subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, a strength test, and an anodizability evaluation test. The procedures and criteria of the respective tests are as in First Experimental Example.
- The average crystal grain sizes of the thick plates were determined in the same manner as in First Experimental Example, because the crystal grain size of a thick plate affects the anodizability thereof.
- The test results are shown in Tables 22 and 23.
-
[Table 22] Category Number Flatness Accuracy of plate thickness Strength Appearance after anodization Cross section structure (mm/m) Evaluation Evaluation Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Average crystal grain size (µm) Example Alloy 1C 0.24 Accepted Excellent 218 103 Accepted Accepted Accepted 170 Alloy 2C 0.24 Accepted Excellent 229 112 Accepted Accepted Accepted 170 Alloy 3C 0.27 Accepted Excellent 309 147 Accepted Accepted Accepted 160 Alloy 4C 0.27 Accepted Excellent 336 173 Accepted Accepted Accepted 140 Alloy 5C 0.29 Accepted Excellent 384 185 Accepted Accepted Accepted 140 Alloy 6C 0.27 Accepted Excellent 315 142 Accepted Accepted Accepted 160 Alloy 7C 0.25 Accepted Excellent 310 148 Accepted Accepted Accepted 160 Alloy 8C 0.26 Accepted Excellent 320 149 Accepted Accepted Accepted 160 Alloy 9C 0.27 Accepted Excellent 323 158 Accepted Accepted Accepted 160 Alloy 10C 0.28 Accepted Excellent 308 149 Accepted Accepted Accepted 160 Alloy 11C 0.25 Accepted Excellent 228 113 Accepted Accepted Accepted 150 Sliced Sample Alloy 12C 0.27 Accepted Excellent 310 147 Accepted Accepted Accepted 160 Comparative Example Alloy 13C 0.24 Accepted Excellent 176 72 Failed Accented Accepted 220 Alloy 14C unproducible due to the generation of casting cracks Alloy 15C 0.28 Accepted Excellent 315 153 Accepted Failed Accepted 160 Alloy 16C 0.30 Accepted Excellent 314 154 Accepted Failed Accepted 160 Alloy 17C 0.28 Accepted Excellent 327 169 Accepted Accepted Accepted 160 Alloy 18C 0.28 Accepted Excellent 330 167 Accepted Failed Accepted 130 Alloy 19C 0.27 Accepted Excellent 330 163 Accepted Failed Accepted 130 Alloy 20C 0.27 Accepted Excellent 310 151 Accepted Accepted Accepted 150 Alloy 21C 0.28 Accepted Excellent 320 156 Accepted Accepted Accepted 130 Alloy 22C 0.27 Accepted Excellent 320 158 Accepted Accepted Accepted 160 -
[Table 23] Category Number Flatness Accuracy of plate thickness Strength Appearance after anodization Cross section structure (mm/m) Evaluation Evaluation Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Average crystal grain size (µm) Alloy 1C 0.43 Failed Excellent 218 105 Accepted Accepted Failed 160 Alloy 2C 0.44 Failed Excellent 227 110 Accepted Accepted Failed 150 Alloy 3C 0.48 Failed Accepted 297 141 Accepted Accepted Failed 140 Alloy 4C 0.61 Failed Accepted 314 163 Accepted Accepted Failed 120 Alloy 5C 0.70 Failed Accepted 383 200 Accepted Accepted Failed 140 Alloy 6C 0.48 Failed Excellent 304 157 Accepted Accepted Failed 150 Alloy 7C 0.48 Failed Accepted 298 151 Accepted Accepted Failed 150 Alloy 8C 0.48 Failed Accepted 297 150 Accepted Accepted Failed 140 Alloy 9C 0.52 Failed Accepted 313 159 Accepted Accepted Failed 140 Alloy 10C 0.50 Failed Accepted 303 146 Accepted Accepted Failed 150 Alloy 11C 0.43 Failed Excellent 225 129 Accepted Accepted Failed 160 Hot-rolled Sample Comparative Example Alloy 12C 0.49 Failed Accepted 306 161 Accepted Accepted Failed 140 Alloy 13C 0.42 Failed Excellent 181 97 Accepted Accepted Failed 200 Alloy 14C unproducible due to the generation of casting cracks Alloy 15C 0.50 Failed Excellent 299 142 Accepted Failed Failed 160 Alloy 16C 0.49 Failed Accepted 298 143 Accepted Failed Failed 160 Alloy 17C 0.49 Failed Accepted 307 156 Accepted Accepted Failed 150 Alloy 18C 0.49 Failed Excellent 312 156 Accepted Failed Failed 140 Alloy 19C 0.49 Failed Accepted 310 152 Accepted Failed Failed 130 Alloy 20C 0.49 Failed Accepted 295 142 Accepted Accepted Failed 150 Alloy 21C 0.50 Failed Accepted 299 144 Accepted Accepted Failed 150 Alloy 22C 0.50 Failed Accepted 303 152 Accepted Accepted Failed 150 - Table 22 shows the test results of the sliced samples, in which the samples using Alloys 1C to 12C correspond to examples according to the ninth embodiment of the present invention; while the samples using Alloys 13C to 22C correspond to comparative examples. Table 23 shows the test results of the hot-rolled samples, in which all the samples using Alloys 1C to 22C correspond to comparative examples.
- As is demonstrated in Table 22, the samples using Alloys 1C to 13C and 15C to 22C had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
The sample using Alloy 14C contained Mg in a content of more than the upper limit in the material aluminum alloy, suffered from casting cracks, and was unproducible. The sample using Alloy 13C contained Mg in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
The samples using Alloys 1C to 13C, 17C, and 20C to 22C did not suffer from unevenness in their appearances of surfaces after anodization The samples using Alloys 15C, 16C, 18C, and 19C contained Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 1C to 13C and 15C to 22C did not suffer from unevenness in their appearances of cross sections after anodization.
The samples using Alloys 17C, 20C, 21C, and 22C contained Cu, Zn, Ti, and Zr, respectively, in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency. - As is demonstrated in Table 23, the samples using Alloys 1C to 13C and 15C to 22C suffered from accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them were somewhat inferior in accuracy of plate thickness to the corresponding sliced samples.
The sample using Alloy 14C contained Mg in a content of more than the upper limit in the material aluminum alloy, suffered from casting cracks, and was unproducible. The sample using Alloy 13C contained Mg in a content of less than the lower limit in the material aluminum alloy and showed insufficient strength.
The samples using Alloy 15C, 16C, 18C, and 19C contain Si, Fe, Mn, and Cr, respectively, in a content of more than the upper limit, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 1C to 13C and 15C to 22C suffered from unevenness in their appearances of cross sections after anodization. - This experimental example relates to the ninth embodiment of the present invention. The experimental example used Alloy 3C in Table 21.
- Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloy 3C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, the slabs were subjected to a slicing step to give sliced samples. The sliced samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
Next, the sliced samples were further subjected to a heat treatment step, in which they were subjected to a heat treatment under conditions given in Table 24. -
[Table 24] Category Number Heat treatment Flatness Accuracy of plate thickness Chip breakability upon cutting (mm/m) Evaluation Evaluation (number/ 10 g) Evaluation Sliced Sample Example C1 Alloy 3C 350°C for 2 hr 0.26 Accepted Excellent 1040 Accepted C2 Alloy 3C 250°C for 4 hr 0.34 Accepted Excellent 1170 Accepted Comparative Example C3 Alloy 3C none 0.45 Failed Accepted 1340 Accepted C4 Alloy 3C 420°C for 4 hr 0.23 Accepted Excellent 950 Failed C5 Alloy 3C 150°C for 2 hr 0.42 Failed Accepted 1280 Accepted - Accordingly, Samples C1 and C2, whose heat treatment conditions satisfy the conditions specified in the ninth embodiment of the present invention, correspond to examples according to the ninth embodiment of the present invention; while Samples C3 to C5, whose heat treatment conditions do not satisfy the conditions specified in the ninth embodiment of the present invention, correspond to comparative examples.
- The sliced samples after the treatments were subjected to a flatness evaluation test and an evaluation test for accuracy of plate thickness.
- In the flatness evaluation, the samples were tested to determine their amounts of warpage (flatness) per 1 m in the casting direction. Samples having an amount of warpage of 0.4 mm or less per 1 m length were evaluated as having accepted flatness (Accepted), while those having an amount of warpage of more than 0.4 mm per 1 m length were evaluated as having unaccepted flatness (Failed).
- The evaluation test for accuracy of plate thickness is as in First Experimental Example.
- The cutting property evaluation test is as in Seventh Experimental Example.
- The test results are shown in Table 24.
- As is demonstrated in Table 24, Examples C1 and C2, whose heat treatment conditions satisfy the conditions specified in the ninth embodiment of the present invention, excelled in flatness, accuracy of plate thickness, and cutting property. Comparative Example C3, which did not undergo a heat treatment, showed poor flatness, and had somewhat inferior accuracy of plate thickness to Examples C1 and C2. Comparative Example C4 had been thermally treated at a temperature higher than the range specified in the ninth embodiment of the present invention and thereby showed poor cutting property. Comparative Example C5 had been thermally treated at a temperature lower than the range specified in the ninth embodiment of the present invention, thereby showed poor flatness, and was somewhat inferior in accuracy of plate thickness to Examples C1 and C2.
- This experimental example relates to the tenth embodiment of the present invention. The experimental example used 3000 series Al-Mn alloys as the aluminum alloys.
- With reference to Table 25, Alloys 23C and 24C were used as example alloys; while Alloys 25C and 26C were used as comparative example alloys.
-
[Table 25] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy 23C - 0.1 0.3 - 0.5 - - 0.0 1 - 3000 series Alloy 24C - 0.1 0.4 - 0.9 - - 0.0 1 - 3000 series Comparative Example Alloy Alloy 25C - 0.1 0.4 - 0.2 - - 0.0 1 - 3000 series Mn content less than lower limit Alloy 26C - 0.1 0.3 - 1.7 - - 0.0 1 - 3000 series Mn content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 23C to 26C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, sliced samples and hot-rolled samples were prepared from the slabs. The sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
Next, the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 350°C for 4 hours. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the tenth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 23C and 24C correspond to examples according to the tenth embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments were subjected to a flatness evaluation test, an evaluation test for accuracy of plate thickness, a strength test, and an anodizability evaluation test.
- The procedures and criteria of the respective tests are as in First Experimental Example.
However, the properties of thick plates vary depending on the type of alloy used, and the criteria for the strength were modified as follows. Specifically, samples having a tensile strength of 90 N/mm2 or more were evaluated as having accepted strength (Accepted), whereas those having a tensile strength of less than 90N/mm2were evaluated as having unaccepted strength (Failed). - The test results are shown in Table 26.
-
[Table 26] Category Number Flatness Accuracy of plate thickness Strength Appearance after anodization (mm/m) Evaluation Evaluation Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Sliced Sample Example Alloy23C 0.22 Accepted Excellent 98 40 Accepted Accepted Accepted Alloy24C 0.22 Accepted Excellent 102 39 Accepted Accepted Accepted Comparative Example Alloy25C 0.22 Accepted Excellent 86 38 Failed Accepted Accepted Alloy26C 0.23 Accepted Excellent 121 51 Accepted Failed Accepted Hot-rolled Sample Comparative Example Alloy23C 0.41 Failed Excellent 115 55 Accepted Accepted Failed Alloy24C 0.42 Failed Accepted 118 57 Accepted Accepted Failed Alloy25C 0.41 Failed Excellent 95 46 Accepted Accepted Failed Alloy26C 0.44 Failed Accepted 142 72 Accepted Failed Failed - As is demonstrated in Table 26, the samples using Alloys 23C to 26C had small processing strain and showed little warpage, i.e., they had satisfactory flatness. Additionally, they excelled in accuracy of plate thickness.
The sample using Alloy 25C contained Mn in a content less than the lower limit in the material aluminum alloy and thereby had insufficient strength. The sample using Alloy 26C contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization. The samples using Alloys 23C to 26C did not suffer from unevenness in their appearances of cross sections after anodization. - As is demonstrated in Table 26, the samples using Alloys 23C to 26C suffered from accumulated processing strain and showed large warpage in the rolling direction. Specifically, they showed inferior flatness. Many of them were somewhat inferior in accuracy of plate thickness to the corresponding sliced samples.
The sample using Alloy 25C contained Mn in a content of less than the lower limit in the material aluminum alloy and was thereby somewhat inferior in strength to the other hot-rolled samples. The sample using Alloy 26C contained Mn in a content of more than the upper limit in the material aluminum alloy, thereby caused coarse intermetallic compounds, and suffered from unevenness in its appearance of surface after anodization. The samples using Alloys 23C to 26C suffered from unevenness in their appearances of cross sections after anodization. - This experimental example relates to the eleventh embodiment of the present invention. The experimental example used 6000 series Al-Mg-Si alloys as the aluminum alloys.
- With reference to Table 27, Alloys 27C and 28C were used as example alloys; while Alloys 29C to 32C were used as comparative example alloys.
-
[Table 27] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy27C 0.9 0.5 0.5 0.3 0.1 0.2 0.2 0.02 - 6000 series Alloy28C 0.5 0.9 0.2 - 0.1 - - 0.02 - 6000 series Comparative Example Alloy Alloy29C 0.9 0.1 0.5 - 0.1 - - 0.02 - 6000 series Si content less than lower limit Alloy30C 0.9 1.8 0.4 - 0.1 - - 0.02 - 6000 series Si content more than upper limit Alloy31C 0.2 0.5 0.5 - 0.1 - - 0.02 - 6000 series Mg content less than lower limit Alloy32C 1.7 0.5 0.4 - 0.1 - - 0.02 - 6000 series Mg content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subjecting Alloys 27C to 32C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, sliced samples and hot-rolled samples were prepared from the slabs. The sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subj ecting the slabs to a heat treatment and subsequently to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
Next, the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 350°C for 4 hours.
The resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 520°C and subsequently to an aging treatment at 175°C for 8 hours. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the eleventh embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 27C and 28C correspond to examples according to the eleventh embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments were subjected to a strength test and an anodizability evaluation test.
- The procedures and criteria of the respective tests are as in First Experimental Example.
However, the properties of thick plates vary depending on the type of alloy used, and the criteria for the strength were modified as follows. Specifically, samples having a tensile strength of 200 N/mm2 or more were evaluated as having accepted strength (Accepted) ; while those having a tensile strength of less than 200 N/mm2 were evaluated as having unaccepted strength (Failed). - The test results are shown in Table 28.
-
[Table 28] Category Number Strength Appearance after anodization Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Sliced Sample Example Alloy27C 317 269 Accepted Accepted Accepted Alloy28C 290 247 Accepted Accepted Accepted Comparative Example Alloy29C 110 64 Failed Accepted Accepted Alloy30C 335 298 Accepted Failed Accepted Alloy31C 172 120 Failed Accepted Accepted Alloy32C 209 123 Accepted Accepted Accepted Hot-rolled Sample Comparative Example Alloy27C 343 272 Accepted Accepted Failed Alloy28C 316 272 Accepted Accepted Failed Alloy29C 132 84 Failed Accepted Failed Alloy30C 359 319 Accepted Failed Failed Alloy31C 197 142 Failed Accepted Failed Alloy32C 228 141 Accepted Accepted Failed - As is demonstrated in Table 28, the samples using Alloys 29C and 31C contained Si and Mg, respectively, in a content of less than its lower limit in the material aluminum alloy and showed insufficient strength. The sample using Alloy 30C contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization. The sample using Alloy 32C contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency. The samples using Alloys 27C to 32C did not suffer from unevenness in their appearances of cross sections after anodization.
- As is demonstrated in Table 28, the samples using Alloys 29C and 31C contain Si and Mg, respectively, in a content of less than the lower limit in the material aluminum alloy, and showed insufficient strength. The sample using Alloy 30C contained Si in a content of more than the upper limit in the material aluminum alloy, caused coarse intermetallic compounds, and suffered from unevenness in their appearances of surfaces after anodization. The sample using Alloy 32C contained Mg in a content of more than the upper limit in the material aluminum alloy, and advantages obtained therefrom were saturated, resulting in inferior economical efficiency. The samples using Alloy 27C to 32C suffered from unevenness in their appearances of cross sections after anodization.
- This experimental example relates to the twelfth embodiment of the present invention. The experimental example used 7000 series Al-Zn-Mg alloys as the aluminum alloys.
- With reference to Table 29, Alloys 33C and 34C were used as example alloys; while Alloys 35C to 38C were used as comparative example alloys.
-
[Table 29] Category Number Element (percent by mass) Alloy type Remarks Mg Si Fe Cu Mn Cr Zn Ti Zr Example Alloy Alloy33C 2.4 0.1 0.2 1.8 - 0.2 4.0 0.02 - 7000 series Alloy34C 3.6 0.2 0.2 2.0 - - 8.0 0.02 0.2 7000 series Comparative Example Alloy Alloy35C 0.3 0.1 0.2 2.2 - 0.1 4.0 0.02 - 7000 series Mg content less than lower limit Alloy36C 5.2 0.2 0.2 2.0 - 0.1 5.0 0.02 - 7000 series Mg content more than upper limit Alloy37C 2.4 0.1 0.2 2.2 - 0.1 2.4 0.02 - 7000 series Zn contentless than lower limit Alloy38C 3.0 0.2 0.2 2.0 - 0.1 9.3 0.02 - 7000 series Zn content more than upper limit - Initially, a series of slabs having a plate thickness of 500 mm was prepared by subj ecting Alloys 33C to 38C to a melting step, a hydrogen gas removal step, a filtration step, and a casting step sequentially in this order.
Next, sliced samples and hot-rolled samples were prepared from the slabs. The sliced samples were prepared by subjecting the slabs to a slicing step, while the hot-rolled samples were prepared by subjecting the slabs to a heat treatment and subsequently to hot rolling. The sliced samples and hot-rolled samples are aluminum alloy thick plates each 20 mm thick, 1000 mm wide, and 2000 mm long.
Next, the sliced samples were further subjected to a heat treatment step in which they were held at a temperature of 300°C for 4 hours.
The resulting sliced samples and hot-rolled samples were further subjected to a solution treatment at 470°C and subsequently to an aging treatment at 120°C for 48 hours. - Accordingly, the sliced samples after these treatments are aluminum alloy thick plates manufactured by the procedures of the manufacturing method according to the twelfth embodiment of the present invention, whereas the hot-rolled samples after the treatments are not. Among them, only the sliced samples using Alloys 33C and 34C correspond to examples according to the twelfth embodiment of the present invention.
- Next, the sliced samples and hot-rolled samples after the treatments were subjected to a strength test and an anodizability evaluation test.
- The procedures and criteria of the respective tests are as in First Experimental Example.
However, the properties of thick plates vary depending on the type of alloy used, and the criteria for the strength were modified as follows. Specifically, samples having a tensile strength of 250 N/mm2 or more were evaluated as having accepted strength (Accepted) ; while those having a tensile strength of less than 250 N/mm2 were evaluated as having unaccepted strength (Failed). - The test results are shown in Table 30.
-
[Table 30] Category Number Strength Appearance after anodization Tensile strength
(N/mm2)Proof stress
(N/mm2)Evaluation Surface appearance Cross section appearance Sliced Sample Example Alloy 33C 418 360 Accepted Accepted Accepted Alloy 34C 520 453 Accepted Accepted Accepted Comparative Example Alloy 35C 189 162 Failed Accepted Accepted Alloy 36C 290 190 Accepted Failed Accepted Alloy 37C 208 131 Failed Accepted Accepted Alloy 38C 614 530 Accepted Failed Accepted Hot-rolled Sample Comparative Example Alloy 33C 437 378 Accepted Accepted Failed Alloy 34C 549 478 Accepted Accepted Failed Alloy 35C 204 169 Failed Accepted Failed Alloy 36C 305 204 Accepted Failed Failed Alloy 37C 230 150 Failed Accepted Failed Alloy 38C 628 542 Accepted Failed Failed - As is demonstrated in Table 30, the samples using Alloys 35C and 37C contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy, and showed insufficient strength. The samples using Alloys 36C and 38C contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminumalloy, and thereby suf fered fromunevenness in their appearances of surfaces after anodization. The samples using Alloys 33C to 38C did not suffer from unevenness in their appearances of cross sections after anodization.
- As is demonstrated in Table 30, the samples using Alloys 35C and 37C contained Mg and Zn, respectively, in a content of less than the lower limit in the material aluminum alloy, and thereby showed insufficient strength. The samples using Alloys 36C and 38C contained Mg and Zn, respectively, in a content of more than the upper limit in the material aluminum alloy and thereby suffered from unevenness in their appearances of surfaces after anodization. The samples using Alloys 33C to 38C suffered from unevenness in their appearances of cross sections after anodization.
- Methods for manufacturing aluminum alloy thick plates, according to the present invention, show superior productivity, can easily control the surface condition and flatness to improve the accuracy of plate thickness, and are thereby industrially very useful.
Claims (22)
- A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; anda heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 400°C or higher but lower than its melting point for one hour or longer. - A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; anda heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 400°C or higher but lower than its melting point for one hour or longer. - A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further containing at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0. 6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; anda heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 400°C or higher but lower than its melting point for one hour or longer. - A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9. 0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3. 0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; anda heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 350°C or higher but lower than its melting point for one hour or longer. - The method for manufacturing an aluminum alloy thick plate, according to any one of claims 1 to 4, further comprising, subsequent to the heat treatment step, a surface smoothing treatment step of subjecting the surface of the aluminum alloy thick plate to a surface smoothing treatment.
- The method for manufacturing an aluminum alloy thick plate, according to claim 5, wherein the surface smoothing treatment is carried out by at least one process selected from the group consisting of cutting, grinding, and polishing.
- The method for manufacturing an aluminum alloy thick plate, according to any one of claims 1 to 4, wherein the slicing step comprises removing a central portion in a thickness direction from the slab, the central portion having two substantially identical thicknesses in the thickness direction from the center of the thickness direction to the both surfaces of the central portion, respectively, and having a total thickness of from one-thirtieth to one-fifth the thickness T of the slab (T/30 to T/5).
- A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further containing at least one memberselected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainderbeing aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer; anda slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness. - A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer; anda slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness. - A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further containing at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0. 6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer; anda slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness. - A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9. 0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a heat treatment step of thermally treating the slab by holding the same at a temperature of 200°C or higher but lower than 350°C for one hour or longer; anda slicing step of slicing the thermally treated slab into an aluminum alloy thick plate having a predetermined thickness. - The method for manufacturing an aluminum alloy thick plate, according to any one of claims 8 to 11, further comprising, subsequent to the slicing step, a surface smoothing treatment step of subjecting the surface of the aluminum alloy thick plate having a predetermined thickness to a surface smoothing treatment.
- The method for manufacturing an aluminum alloy thick plate, according to claim 12, wherein the surface smoothing treatment is carried out by at least one process selected from the group consisting of cutting, grinding, and polishing.
- The method for manufacturing an aluminum alloy thick plate, according to any one of claims 8 to 11, wherein the slicing step comprises removing a central portion in a thickness direction from the slab, the central portion having two substantially identical thicknesses in the thickness direction from the center of the thickness direction to the both surfaces of the central portion, respectively, and having a total thickness of from one-thirtieth to one-fifth the thickness T of the slab (T/30 to T/5).
- A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Mg in a content of 1.5 percent by mass or more and 12.0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.6 percent by mass or less, Mn in a content of 1.0 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; anda heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer. - A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Mn in a content of 0.3 percent by mass or more and 1.6 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 0.5 percent by mass or less, Mg in a content of 1.5 percent by mass or less, Cr in a content of 0.3 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; anda heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer. - A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Si in a content of 0.2 percent by mass or more and 1.6 percent by mass or less and Mg in a content of 0.3 percent by mass or more and 1.5 percent by mass or less, and further containing at least one member selected from the group consisting of Fe in a content of 0.8 percent by mass or less, Cu in a content of 1.0 percent by mass or less, Mn in a content of 0. 6 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Zn in a content of 0.4 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.3 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness; anda heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 400°C for one hour or longer. - A method for manufacturing an aluminum alloy thick plate from an aluminum alloy,
the aluminum alloy containing Mg in a content of 0.4 percent by mass or more and 4.0 percent by mass or less and Zn in a content of 3.0 percent by mass or more and 9. 0 percent by mass or less, and further containing at least one member selected from the group consisting of Si in a content of 0.7 percent by mass or less, Fe in a content of 0.8 percent by mass or less, Cu in a content of 3.0 percent by mass or less, Mn in a content of 0.8 percent by mass or less, Cr in a content of 0.5 percent by mass or less, Ti in a content of 0.1 percent by mass or less, and Zr in a content of 0.25 percent by mass or less, with the remainder being aluminum and inevitable impurities,
the method comprising in the following order:a melting step of melting the aluminum alloy;a hydrogen gas removal step of removing hydrogen gas from the molten aluminum alloy;a filtration step of filtering the aluminum alloy, from which hydrogen gas have been removed, to remove inclusions from the aluminum alloy;a casting step of casting the aluminum alloy, from which inclusions have been removed, into a slab;a slicing step of slicing the slab into an aluminum alloy thick plate having a predetermined thickness;a heat treatment step of thermally treating the aluminum alloy thick plate having a predetermined thickness by holding the same at a temperature of 200°C or higher but lower than 350°C for one hour or longer. - The method for manufacturing an aluminum alloy thick plate, according to any one of claims 15 to 18, further comprising, subsequent to the heat treatment step, a surface smoothing treatment step of subjecting the surface of the aluminum alloy thick plate to a surface smoothing treatment.
- The method for manufacturing an aluminum alloy thick plate, according to claim 19, wherein the surface smoothing treatment is carried out by at least one process selected from the group consisting of cutting, grinding, and polishing.
- The method for manufacturing an aluminum alloy thick plate, according to any one of claims 15 to 18, the slicing step comprises removing a central portion in a thickness direction from the slab, the central portion having two substantially identical thicknesses in the thickness direction from the center of the thickness direction to the both surfaces of the central portion, respectively, and having a total thickness of from one-thirtieth to one-fifth the thickness T of the slab (T/30 to T/5).
- An aluminum alloy thick plate manufactured by the method for manufacturing an aluminum alloy thick plate, according to any one of claims 1 to 4, claims 8 to 11, and claims 15 to 18, the aluminum alloy thick plate comprising crystal grains having an average grain size of 400 µm or less.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007095423A JP4231530B2 (en) | 2007-03-30 | 2007-03-30 | Aluminum alloy plate manufacturing method and aluminum alloy plate |
JP2007095419A JP4231529B2 (en) | 2007-03-30 | 2007-03-30 | Aluminum alloy plate manufacturing method and aluminum alloy plate |
JP2007098495A JP4242429B2 (en) | 2007-04-04 | 2007-04-04 | Aluminum alloy plate manufacturing method and aluminum alloy plate |
PCT/JP2008/055873 WO2008123355A1 (en) | 2007-03-30 | 2008-03-27 | Method for producing aluminum alloy thick plate and aluminum alloy thick plate |
Publications (4)
Publication Number | Publication Date |
---|---|
EP2130931A1 true EP2130931A1 (en) | 2009-12-09 |
EP2130931A4 EP2130931A4 (en) | 2011-03-23 |
EP2130931B1 EP2130931B1 (en) | 2019-09-18 |
EP2130931B2 EP2130931B2 (en) | 2022-08-03 |
Family
ID=39830843
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08722912.6A Active EP2130931B2 (en) | 2007-03-30 | 2008-03-27 | Method for producing aluminum alloy thick plate |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP2130931B2 (en) |
KR (2) | KR101151563B1 (en) |
TW (2) | TWI468527B (en) |
WO (1) | WO2008123355A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2263811A1 (en) * | 2008-03-28 | 2010-12-22 | Kabushiki Kaisha Kobe Seiko Sho | Aluminum alloy plate and process for producing the same |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108474066A (en) | 2015-12-18 | 2018-08-31 | 诺维尔里斯公司 | High intensity 6XXX aluminium alloys and its manufacturing method |
KR102063133B1 (en) | 2015-12-18 | 2020-01-07 | 노벨리스 인크. | High-strength 6xxx aluminum alloys and methods of making the same |
KR102302492B1 (en) * | 2017-03-03 | 2021-09-15 | 가부시키가이샤 유에이씨제이 | aluminum alloy plate |
WO2019222236A1 (en) | 2018-05-15 | 2019-11-21 | Novelis Inc. | High strength 6xxx and 7xxx aluminum alloys and methods of making the same |
CN114574737B (en) * | 2020-12-01 | 2022-11-22 | 中国科学院金属研究所 | High-strength high-plasticity stress corrosion resistant nano-structure aluminum alloy and preparation method thereof |
TWI830452B (en) | 2022-10-21 | 2024-01-21 | 財團法人工業技術研究院 | Aluminum alloy material, aluminum alloy object and method for manufacturing the same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004085096A1 (en) * | 2003-03-26 | 2004-10-07 | Showa Denko K.K. | Horizontally continuously cast rod of aluminum alloy and method and equipment for producing the rod. |
EP2034035A1 (en) * | 2006-05-18 | 2009-03-11 | Kabushiki Kaisha Kobe Seiko Sho | Process for producing aluminum alloy plate and aluminum alloy plate |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0639664B2 (en) * | 1989-08-24 | 1994-05-25 | 日本軽金属株式会社 | Manufacturing method of aluminum alloy material for laser mirror |
US5489363A (en) | 1993-05-04 | 1996-02-06 | Kamyr, Inc. | Pulping with low dissolved solids for improved pulp strength |
JP3552577B2 (en) | 1999-03-16 | 2004-08-11 | 日本軽金属株式会社 | Aluminum alloy piston excellent in high temperature fatigue strength and wear resistance and method of manufacturing the same |
JP2002146447A (en) | 2000-11-01 | 2002-05-22 | Daido Steel Co Ltd | Degassing apparatus for non-ferrous metal |
US20050006010A1 (en) | 2002-06-24 | 2005-01-13 | Rinze Benedictus | Method for producing a high strength Al-Zn-Mg-Cu alloy |
JP4278052B2 (en) | 2003-03-26 | 2009-06-10 | 昭和電工株式会社 | Aluminum alloy horizontal continuous casting rod manufacturing method |
JP4214840B2 (en) * | 2003-06-06 | 2009-01-28 | 住友金属工業株式会社 | High-strength steel sheet and manufacturing method thereof |
JP2005344173A (en) | 2004-06-03 | 2005-12-15 | Kobe Steel Ltd | Aluminum-alloy substrate for magnetic disk, and its manufacturing method |
JP2007051310A (en) * | 2005-08-15 | 2007-03-01 | Furukawa Sky Kk | Aluminum alloy sheet for aluminum bottle can barrel, and its manufacturing method |
JP4515363B2 (en) * | 2005-09-15 | 2010-07-28 | 株式会社神戸製鋼所 | Aluminum alloy plate excellent in formability and method for producing the same |
JP4955969B2 (en) | 2005-09-16 | 2012-06-20 | 株式会社神戸製鋼所 | Manufacturing method of forming aluminum alloy sheet |
CN100478476C (en) * | 2006-07-14 | 2009-04-15 | 中国铝业股份有限公司 | High strength aluminium alloy wire and rod and their prepn process |
-
2008
- 2008-03-27 KR KR1020097020395A patent/KR101151563B1/en active IP Right Grant
- 2008-03-27 KR KR1020117023623A patent/KR101197952B1/en active IP Right Grant
- 2008-03-27 WO PCT/JP2008/055873 patent/WO2008123355A1/en active Application Filing
- 2008-03-27 EP EP08722912.6A patent/EP2130931B2/en active Active
- 2008-03-28 TW TW101129190A patent/TWI468527B/en not_active IP Right Cessation
- 2008-03-28 TW TW097111205A patent/TWI383053B/en not_active IP Right Cessation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004085096A1 (en) * | 2003-03-26 | 2004-10-07 | Showa Denko K.K. | Horizontally continuously cast rod of aluminum alloy and method and equipment for producing the rod. |
EP2034035A1 (en) * | 2006-05-18 | 2009-03-11 | Kabushiki Kaisha Kobe Seiko Sho | Process for producing aluminum alloy plate and aluminum alloy plate |
Non-Patent Citations (2)
Title |
---|
DATABASE WPI Week 199036 Thomson Scientific, London, GB; AN 1990-272772 XP002622453, & JP 2 194152 A (NIPPON LIGHT METAL CO) 31 July 1990 (1990-07-31) * |
See also references of WO2008123355A1 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2263811A1 (en) * | 2008-03-28 | 2010-12-22 | Kabushiki Kaisha Kobe Seiko Sho | Aluminum alloy plate and process for producing the same |
EP2263811A4 (en) * | 2008-03-28 | 2011-05-04 | Kobe Steel Ltd | Aluminum alloy plate and process for producing the same |
Also Published As
Publication number | Publication date |
---|---|
TW200900512A (en) | 2009-01-01 |
TWI468527B (en) | 2015-01-11 |
KR101151563B1 (en) | 2012-05-30 |
KR101197952B1 (en) | 2012-11-05 |
TW201245462A (en) | 2012-11-16 |
EP2130931A4 (en) | 2011-03-23 |
EP2130931B2 (en) | 2022-08-03 |
WO2008123355A1 (en) | 2008-10-16 |
TWI383053B (en) | 2013-01-21 |
EP2130931B1 (en) | 2019-09-18 |
KR20090117951A (en) | 2009-11-16 |
KR20110118186A (en) | 2011-10-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2034035B2 (en) | Process for producing aluminum alloy plate | |
CN101605916B (en) | Method for manufacturing aluminum alloy thick plate, and aluminum alloy thick plate | |
JP4174524B2 (en) | Aluminum alloy plate manufacturing method and aluminum alloy plate | |
EP2130931A1 (en) | Method for producing aluminum alloy thick plate and aluminum alloy thick plate | |
EP2811042B1 (en) | ALUMINiUM ALLOY forged MATERIAL AND METHOD FOR manufacturING the SAME | |
EP2263811A1 (en) | Aluminum alloy plate and process for producing the same | |
CN109563572B (en) | Aluminum alloy plate for magnetic disk substrate, method for producing same, and magnetic disk | |
KR101731688B1 (en) | Method for surface brazing between aluminum alloy member and copper alloy member | |
US20130302643A1 (en) | Aluminium alloy free from si primary particles | |
EP0948663B1 (en) | Cathode pulverisation targets in aluminium alloy | |
JP4174526B2 (en) | Aluminum alloy plate manufacturing method and aluminum alloy plate | |
KR20130109224A (en) | Aluminum alloy sheet for battery case having good moldability and weldability | |
JP4740941B2 (en) | Method for producing aluminum alloy plate | |
JP4231530B2 (en) | Aluminum alloy plate manufacturing method and aluminum alloy plate | |
JP4174527B2 (en) | Aluminum alloy plate manufacturing method and aluminum alloy plate | |
JP4242429B2 (en) | Aluminum alloy plate manufacturing method and aluminum alloy plate | |
JP4174525B2 (en) | Aluminum alloy plate manufacturing method and aluminum alloy plate | |
CN115298336B (en) | Technique for producing aluminum alloy products with improved formability and recyclability | |
JP2023032363A (en) | Method for producing aluminum alloy ingot for magnetic disk, method for producing aluminum alloy plate for magnetic disk using the aluminum alloy ingot, method for producing aluminum alloy substrate for magnetic disk using the aluminum alloy plate, and magnetic disk using the aluminum alloy substrate | |
CN118186257A (en) | Aluminum alloy, aluminum alloy product for PCB drilling and method for manufacturing aluminum alloy | |
CN117580967A (en) | Aluminum alloy sheet for magnetic disk, aluminum alloy blank for magnetic disk, and aluminum alloy substrate for magnetic disk |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20090709 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: KATO, TOMOHARU Inventor name: KOBAYASHI, KAZUNORI Inventor name: TOKUDA, KENJI Inventor name: INABA, TAKASHI |
|
DAX | Request for extension of the european patent (deleted) | ||
A4 | Supplementary search report drawn up and despatched |
Effective date: 20110223 |
|
17Q | First examination report despatched |
Effective date: 20111208 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C22F 1/053 20060101ALI20150421BHEP Ipc: C22C 21/10 20060101ALI20150421BHEP Ipc: B22D 21/04 20060101ALI20150421BHEP Ipc: B22D 43/00 20060101ALI20150421BHEP Ipc: B22D 21/00 20060101AFI20150421BHEP Ipc: C22B 9/02 20060101ALI20150421BHEP Ipc: C22F 1/05 20060101ALI20150421BHEP Ipc: C22F 1/04 20060101ALI20150421BHEP Ipc: B22D 1/00 20060101ALI20150421BHEP Ipc: C22F 1/047 20060101ALI20150421BHEP Ipc: C22B 9/05 20060101ALI20150421BHEP Ipc: C22C 21/02 20060101ALI20150421BHEP Ipc: C22F 1/00 20060101ALI20150421BHEP Ipc: C22C 1/02 20060101ALI20150421BHEP Ipc: C22B 21/06 20060101ALI20150421BHEP Ipc: C22C 21/06 20060101ALI20150421BHEP Ipc: C22C 21/00 20060101ALI20150421BHEP |
|
GRAJ | Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted |
Free format text: ORIGINAL CODE: EPIDOSDIGR1 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
INTG | Intention to grant announced |
Effective date: 20150702 |
|
INTC | Intention to grant announced (deleted) | ||
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
INTG | Intention to grant announced |
Effective date: 20190401 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP Ref country code: CH Ref legal event code: NV Representative=s name: E. BLUM AND CO. AG PATENT- UND MARKENANWAELTE , CH |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602008061216 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: REF Ref document number: 1180707 Country of ref document: AT Kind code of ref document: T Effective date: 20191015 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20190918 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191218 Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191218 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20191219 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 1180707 Country of ref document: AT Kind code of ref document: T Effective date: 20190918 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200120 Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: PL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200224 Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R026 Ref document number: 602008061216 Country of ref document: DE |
|
PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
PLAX | Notice of opposition and request to file observation + time limit sent |
Free format text: ORIGINAL CODE: EPIDOSNOBS2 |
|
26 | Opposition filed |
Opponent name: C-TEC CONSTELLIUM TECHNOLOGY CENTER / CONSTELLIUM NEUF-BRISACH Effective date: 20200616 |
|
PG2D | Information on lapse in contracting state deleted |
Ref country code: IS |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200119 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 |
|
PLAF | Information modified related to communication of a notice of opposition and request to file observations + time limit |
Free format text: ORIGINAL CODE: EPIDOSCOBS2 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: MM Effective date: 20200331 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200327 |
|
PLBB | Reply of patent proprietor to notice(s) of opposition received |
Free format text: ORIGINAL CODE: EPIDOSNOBS3 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200327 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200331 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20200327 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200327 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20220203 Year of fee payment: 15 Ref country code: CH Payment date: 20220215 Year of fee payment: 15 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190918 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20220209 Year of fee payment: 15 |
|
PUAH | Patent maintained in amended form |
Free format text: ORIGINAL CODE: 0009272 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: PATENT MAINTAINED AS AMENDED |
|
27A | Patent maintained in amended form |
Effective date: 20220803 |
|
AK | Designated contracting states |
Kind code of ref document: B2 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R102 Ref document number: 602008061216 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 602008061216 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20230331 Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20230331 Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20231003 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20230331 |