CA2444460C - Hot-dip zn plated steel sheet excellent in luster-retaining property and method of producing the same - Google Patents
Hot-dip zn plated steel sheet excellent in luster-retaining property and method of producing the same Download PDFInfo
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- CA2444460C CA2444460C CA002444460A CA2444460A CA2444460C CA 2444460 C CA2444460 C CA 2444460C CA 002444460 A CA002444460 A CA 002444460A CA 2444460 A CA2444460 A CA 2444460A CA 2444460 C CA2444460 C CA 2444460C
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- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 112
- 239000010959 steel Substances 0.000 title claims abstract description 112
- 238000000034 method Methods 0.000 title claims description 20
- 238000007747 plating Methods 0.000 claims abstract description 148
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 126
- 239000010410 layer Substances 0.000 claims abstract description 83
- 238000001816 cooling Methods 0.000 claims abstract description 57
- 239000002932 luster Substances 0.000 claims abstract description 40
- 230000015556 catabolic process Effects 0.000 claims abstract description 38
- 238000006731 degradation reaction Methods 0.000 claims abstract description 38
- 230000001590 oxidative effect Effects 0.000 claims abstract description 33
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 18
- 239000002344 surface layer Substances 0.000 claims abstract description 13
- 238000010791 quenching Methods 0.000 claims description 61
- 230000000171 quenching effect Effects 0.000 claims description 61
- 239000013078 crystal Substances 0.000 claims description 33
- 230000005496 eutectics Effects 0.000 claims description 20
- 230000000694 effects Effects 0.000 claims description 14
- 239000011159 matrix material Substances 0.000 claims description 14
- 229910052710 silicon Inorganic materials 0.000 claims description 14
- 229910052727 yttrium Inorganic materials 0.000 claims description 14
- 229910052726 zirconium Inorganic materials 0.000 claims description 14
- 239000012535 impurity Substances 0.000 claims description 13
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 10
- 238000007711 solidification Methods 0.000 abstract description 11
- 230000008023 solidification Effects 0.000 abstract description 11
- 229910018134 Al-Mg Inorganic materials 0.000 abstract description 7
- 229910018467 Al—Mg Inorganic materials 0.000 abstract description 7
- 230000003647 oxidation Effects 0.000 abstract description 3
- 238000007254 oxidation reaction Methods 0.000 abstract description 3
- 239000011701 zinc Substances 0.000 description 58
- 239000011777 magnesium Substances 0.000 description 55
- 238000000576 coating method Methods 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 11
- 238000005260 corrosion Methods 0.000 description 11
- 230000007797 corrosion Effects 0.000 description 11
- 239000003595 mist Substances 0.000 description 10
- 230000007423 decrease Effects 0.000 description 9
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 8
- 229910052804 chromium Inorganic materials 0.000 description 8
- 239000011651 chromium Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000012530 fluid Substances 0.000 description 7
- 230000001276 controlling effect Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000002401 inhibitory effect Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 230000008859 change Effects 0.000 description 3
- 238000004532 chromating Methods 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 238000004833 X-ray photoelectron spectroscopy Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 230000003405 preventing effect Effects 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 229910000521 B alloy Inorganic materials 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 238000007739 conversion coating Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- RXCBCUJUGULOGC-UHFFFAOYSA-H dipotassium;tetrafluorotitanium;difluoride Chemical compound [F-].[F-].[F-].[F-].[F-].[F-].[K+].[K+].[Ti+4] RXCBCUJUGULOGC-UHFFFAOYSA-H 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 1
- 229960002261 magnesium phosphate Drugs 0.000 description 1
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 1
- 239000004137 magnesium phosphate Substances 0.000 description 1
- 235000010994 magnesium phosphates Nutrition 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000006557 surface reaction Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- OMQSJNWFFJOIMO-UHFFFAOYSA-J zirconium tetrafluoride Chemical compound F[Zr](F)(F)F OMQSJNWFFJOIMO-UHFFFAOYSA-J 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C18/00—Alloys based on zinc
- C22C18/04—Alloys based on zinc with aluminium as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
- C23C2/06—Zinc or cadmium or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/14—Removing excess of molten coatings; Controlling or regulating the coating thickness
- C23C2/24—Removing excess of molten coatings; Controlling or regulating the coating thickness using magnetic or electric fields
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/26—After-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coating With Molten Metal (AREA)
- Laminated Bodies (AREA)
Abstract
Degradation of the surface luster of a hot-dip Zn-Al-Mg plated steel sheet is inhibited by controlling the contact temperature between the plating layer and a water stream in a water cooling step after plating layer solidification, thereby suitably controlling the strip temperature during contact with the water stream, and further by incorporating a small amount of a suitable readily oxidizing element in the plating bath to stabilize the oxidation state of the plating surface layer Al and Mg.
Description
SPECIFICATION
HOT-DIP ZN PLATED STEEL SHEET EXCELLENT IN LUSTER RETAINING
PROPERTY AND METHOD OF PRODUCING THE SAME
TECHNICAL FIELD
This invention relates to a technology for preventing surface luster degradation that sometimes occurs during production of hot-dip Zn-AI-Mg plated steel sheet using a continuous hot-dip plating line.
BACKGROUND OF THE ART
JP.Hei-l0-226865A, JP.Hei-l0-306357A, USP No. 6,235,410 (US6,235,410 B 1 ) and USP. No. 6,379,820 (US 6,379,820 B 1 ) owned by the applicant of this application teach that a plated steel sheet having corrosion resistance and surface appearance sufficient to meet the requirements of an industrial product can be obtained manufacturing a hot dip Zn-base plated steel sheet using a hot-dip Zn-AI-Mg-system bath composed of AI: 4.0 -%, Mg: 1.0 - 4.0 %, Ti: 0.002 - 0. I %, B: 0.001 - 0.045 % and the balance of Zn and unavoidable impurities, and imparting to the plating layer a metallic swcture including [primary crystal AI phase) and [Zn single phase) in a matrix of [AIIZn/Zn~Mg ternary eutectic crystal structure). The production conditions for obtaining this metallic structure are set out in ttte published specifications.
1n the course of working with such a relatively high Al- and Mg-content hot dip Zn-base plated steel sheet in ensuing production processes, the inventors experienced that, depending on the production conditions, the surface luster of the plating layer deteriorated within two to three days. This surface luster degradation of the plating layer discolors the aesthetically pleasing plated surface just after plating to a somewhat blackish interference color with passage of time (as quickly as 2 - 3 days but sometimes taking 4 - 7 days). The degree of outermost surface layer discoloration (a kind of blackening) can be quantified by measuring the surface brightness. For example, a plating surface that exhibited a brightness (L value) of around L = 82 just after manufacture degrades to around L = 72 in 7 days. Although this decline in L
value does not degrade the corrosion resistance property of the product and does not impair the physical and chemical qualities of the plated steel sheet, it is undesirable from the point of surface appearance. The fact that the surface luster degradation is not uniform over the plating surface, but takes the form of splotchy discoloration, particularly detracts from the aesthetic appeal.
This degradation of surface luster can be considered to be peculiar to plated steel sheets having relatively high AI and Mg content like the hot-dip Zn-Al-Mg plated steel sheets mentioned above. The degree of oxidation of Mg concentrated in the outermost surface layer of the plating and the oxidized state of the surface layer A1 are most likely complexly involved as causes of the degradation. No reports have been published to date regarding the mechanism of the surface luster degradation occurring in such a hot-dip Zn-Al-Mg plated steel sheet or regarding a method for inhibiting the degradation.
OBJECT OF THE INVENTION
An object of the present invention is therefore to provide means for inhibiting the degradation of surface luster that appears as a problem peculiar to hot-dip Zn-Al-Mg plated steel sheet.
DISCLOSURE OE THE INVENTION
The inventors carried out extensive experimentation and research directed to overcoming the foregoing problem. As a result, we determined that the degradation of the surface luster of hot-dip plated steel sheet is caused by the reaction behavior between the plating layer surface and water during water cooling in the cooling step following plating, that one way to prevent the surface luster degradation is to "control the contact temperature between the plating layer and the water stream" in the water cooling step after plating layer solidification, that, by extension, it is effective to suitably control the'"strip temperature during contact with the water stream," and that it is also effective to stabilize the oxidation state of plating surface layer A1 and Mg by incorporating a small amount of a suitable "readily oxidizing element" in the plating bath. By "strip temperature during contact with the water stream" is meant the strip temperature at the time cooling is conducted while forming a water film on the plating layer surface in the cooling step after completion of plating layer solidification. Specifically, it is the plating layer temperature when a water stream is passed onto the completely solidified plating layer and the plating layer is being cooled with a water film formed on the surface of the plating layer.
In other words, according to the inventors' findings, when steel strip is continuously immersed in and withdrawn from a hot-dip Zn-Al-Mg-system bath of the foregoing description and the steel strip is thereafter continuously passed through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream (while providing onto the plating layer surface an amount of water enabling momentary formation of a water film on the plating layer surface), the aforesaid degradation of plating layer surface luster can be inhibited by controlling the strip temperature on the water quenching zone entry side to lower than 105 °C.
The strip temperature on the water quenching zone entry sib, while depending on the equipment conditions, depends strongly on the sheet thickness. When the strip thickness is great, controlling the strip temperature on the water quenching zone entry side to lower than ! OS °C may not be easy. It was found that in such a case, similar inhibition of surface luster degradation can be achieved without lowering the strip temperature on the water quenching zone entry side to lower than 105 °C
(i.e., with the temperature at 105 °C or higher) by adding to the plating bath a small amount of an element that has a very powerful affinity for oxygen (that is a readily oxidizing element) and that has a stabilizing effect on AI oxides. Such elements include, for example, the rare earth elements, Y, Zr and Si. In actual practice, it sutFtces to add about 0.002 - 0.05 mass % of the readily oxidizing element.
Thus, the present invention provides a method of producing a hot-dip Zn plated steel sheet excellent in luster-retaining property comprising a step of continuously immersing and withdrawing steel strip intolfrom a hot-dip Zn base bath containing Al: 4.0 -15 mass % and Mg: 1.0 - 4.0 mass %, thereby forming a plating layer thereon, and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, degradation of the plating layer luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to lower than 105 °C.
The hat.~lip Zn base bath is preferably composed of, in mass %, Al: 4.0 -15 %, Mg: 1.0 -4.0 %, Ti: 0.001 - 0.1 %, B: 0.001 - 0.045 % and the balance of Zn and unavoidable impurities.
The present invention further provides a method of producing a hot-dip Zn plated steel sheet excellent in luster-retaining property comprising a step of continuously immersing and withdrawing steel strip intolfrom a hot-dip Zn base bath containing AI: 4.0 - 15 mass % and Mg: 1.0 - 4.0 mass % and added with 0.002 - 0.05 mass % of at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si, thereby forming a plating layer thereon, and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, degradation of the plating layer surface luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to not lower then 105 °C and not higher than 300 °C. The hot-dip Zn base bath is preferably composed of, in mass %, Al: 4.0 - 15 ~/°, Mg: 1.0 - 4.0 %, Ti: 0.001- 0.1.%, H: 0.001- 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities.
The present invention further provides, as a hot-dip Zn plated steel sheet obtained the foregoing methods, a hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in %
Al: 4.0 -15 % arid Mg: 1.0 - 4.0 %, optionally, Ti: 0.001- 0.1 % and B: 0.001- 0.045 %, preferably, at least one c~eadily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05'/0, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon. The plating layer has a metallic structure inching [primary crystal A1 phase] in a matrix of [AUZn/Zn~Mg ternary eutectic crystal structure] or [primary crystal Al phase], [Zn phase]
and/or [Zn~lVig phase] in a matrix of [AIIZn/ZniMg ternary eutectic crystal structure].
' BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a line diagram schematically illustrating a facility for producing Mg-containing hot-dip Zn plated steel sheet according to the pc~esent invention.
PREFERRED EMBODIMENTS OF THE INVENTION
Generally in this specification, the term "steel strip" is used when explaining the hot-dip plating tine and the term "steel sheet" ;s used when explaining the product. However, the steel strip and steel sheet have the same characteristics.
FIG. 1 schematically illustrates a facility used to produce a hot dip Zn-base plated steel sheet. A steel strip 2 passed through a furnace 1 to be maintained at a prescribed temperature is continuously fed into a plating bath 3. Upon exiting the plating bath 3, the steel strip passes through a wiping nozzle 4 that regulates its coating weight and then through an air jet cooler 5. The plating layer is completely solidified during passage through the air jet cooler 5. The strip next passes through air-water cooling zones 6a, 6b and an air cooling zone 14, any of which may be operated alone or in combination with the others, or not be operated, and then through a water quenching zone 7. It is then temper-rolled in a skin pass mill 8, passed thmugh a tension leveller 9, passed through an inspection step and taken up on a tension reel I0. When chromating or other such chemical treatment is conducted, the steel strip exiting the tension lever 9 is treated in a roll coater I 1, passed through a drying zone 12 and an air cooling zone 13, and taken up on a tension reel 10a.
As explained earlier, when producing a hot-dip Zn-Al-Mg plated steel sheet containing relatively large amounts of A1 and Mg (hereinafter called "Mg-containing hot-dip Zn plated steel sheet', appropriate control of the cooling rate up to complete plating Iayer solidification and of the solidification completion position is essential from the aspect of surface property. For this, the strip feeding speed must be strictly controlled and the strip temperature at the time of passage through the air jet cooler 5 needs to be exactly controlled in accordance with the sheet thickness. Next, so as to enable suitable temper rolling at the skin pass mill 8, the strip temperature at the skin pass entry side needs to be adjusted to a prescribed level (e.g., not more than 70 °C) by cooling conducted at the sir-water cooling zones 6 (and the air cooling zone 14) and/or the water quenching zone 7.
The cooling load at these cooling zones vanes with the strip conning speed and the sheet thickness. Generally, water or a water solution is sprayed at the air-water cooling zones, air is jetted at the air jet cooling zone, and, at the water quenching zone, a water stream - 7 .
adequate for momentarily forming a water film on the plating layer surface is supplied.
Compared with the first mentioned cooling stages, the latter mentioned water quenching zone can achieve a faster cooling rate owing to the contact of the water stream with the plating layer surface. Efficient cooling operation can therefore be conducted at the water quenching zone irrespective of variation in cooling load. Although water or a water solution is sprayed together with an air stream at air-water cooling zone 6, not enough water is supplied to form a water film on the plating layer surface. The cooling is therefore chiefly the result of latent heat extraction by evaporation. This is a different form of heat removal from that by contact with a water stream as in the water quenching tone and therefore differs in cooling rate.
It was found that the luster-retaining property of the plating surface differs depending on strip temperature on the water quenching mne entry side. When the temperature is 105 °C or higher, surface luster degradation readily occurs. While the reason for this is not certain, the inventors concluded that the causes involve such factors as that the reactivity of the plating layer surface is enhanced by the occurrence of a kind of boiling phenomenon when the strip temperature is l 00 °C or higher upon entering the water quenching zone and that the behavior of AI under atmospheric pressure in the presence of water differs above and below about 110 °C, i.e., Ah03 Hi0 (or AIOOH) compound is stable above this temperature while Al=Oj~3H=0 (or AI(OH)3) compound is stable Ixlow this temperature, so that the Al compound formed on the plating layer surface in the water quenching mne differs depending on the entry side steel strip temperature.
In an Mg-containing hot-dip Zn plated steel sheet of the foregoing type having a metallic structure including [primary crystal A1 phase], (Zn phase]
and/or [Zn~lv(g phase] in a matrix of [AUZn/Zn~Mg ternary eutectic crystal structure], the outermost surface of the ternary eutectic crystal structure is changed into a readily oxidizing form by the aforesaid chemical reaction and this is believed to be why surface luster degradation that produces a change in brightness occurs within two or three days after plating.
_g_ At any rate, the inventors discovered that, as demonstrated by the Examples set out later, the surface luster degradation of an Mg-containing hot-dip Zn plated steel sheet can be substantially prevented by regulating the temperature of the steel strip entering the water quenching zone to lower than 105 °C.1n this case, the cooling operation before entry into to the water quenching zone needs to be conduMed not by supplying enough water to the completely solidified plating surface to form a water film that produces quenching, as is done in the water quenching zone, but by a mild cooling operation such as by air-water cooling (mist spraying) or air cooling (e.g.
air jet cooling).
This is because regulation of the steel strip temperature entering the water quenching zone to lower than 105 °C would be meaningless if a quenching operation that forms a water film as is done in the water quenching zone should be conducted before the steel strip enters the water quenching zone. Depending on the sheet thickness and the strip running speed, the strip temperature on the water quenching zone entry side can be regulated to lower-than 105 °C even by air-water cooling.
When the sheet thickness is large, however, it may sometimes be impossible to regulate the strip temperature on the water quenching zone entry side to lower than 105 °C. Although a sufficient amount of cooling in the air-water cooling regions can be achieved even when sheet thickness is large by reducing the strip running speed, this is inadvisable because it leads to problems in solidification point control and lowers productivity. Even when the strip temperature on the water quenching zone entry side is 105 °C or higher, however, surface luster degradation can be effectively inhibited, as is demonstrated by the Examples set out later, by making present at the just completely solidified plating surface an appropriate amount of a readily oxidizing element that hss a very powerful amity for oxygen and a stabilizing effect on At oxides, such as a rare earth element, Y, Zr or Si. In actual practice, it suffices to add about 0.002 -0.05 mass a/o of the readily oxidizing element. Although other elements that exhibit an effect similar to the rare earth elements, Y, Zr and Si may exist, none has yet been identified.
These readily oxidizing elements have a property of concentrating at the outermost surface layer portion of the plating layer during the solidification process of the plating layer of the Mg-containing hot-dip Zn plated steel sheet, or even after solidification.
These elements can therefore reach a relatively high concentration at the outermost surface layer portion even when added to the plating bath in only a small amount. This is thought to enable them to inhibit surface reactions in the water quenching zone which adversely affect the surface luster-maintaining property. When these readily oxidizing elements are added to the plating bath at less than 0.002 %, however, they do not manifest the inhibiting effect. They must therefore be added so as to make their content in the plating bath composition not less than 0.002 mass %. On the other hand, amounts added in excess have poor solubility in the plating bath and even if dissolved only saturate the surface luster degradation inhibiting effect because the elements simply precipitate in excess near the grain boundaries in the plating surface layer portion. The amount added is therefore such that the content in the plating bath becomes not more than 0.10 mass %, in some cases not more than 0,08 mass %, preferably 0.05 mass %, more preferably 0.03 mass %.
The surface luster degradation preventing effect produced by addidan of one or mute reaudily oxidizing elements is acts most effectively when, as explained in the foregoing, the strip temperature on the water quenching zonc entry side is 105 °C or higher.
Even when the strip temperature on the water quenching zone entry side is tower than 105 °C, however, one or more readily oxidizing elements can be added to the plating both to stay an the safe side.
In the case where the strip temperature on the water quenching zone entry side is 105 °C or higher, it should preferably be controlled to not higher than 300 °C
because at higher than 300 °C the cooling load in the water quenching zone becomes so large as to prevent sufficient lowering of the temperature on the skin pass entry side.
In an ordinary production line, if the strip thickness is less than 1.6 mm, the strip temperature on the water quenching zone entry side can be relatively easily made - (0 -lower than 105 °C so as to ensure good luster-retaining property When the strip thickness is 1.6 mm or greater, it is, from the aspect of actual operation, better to ensure lusoer-retaining property by addition of a readily oxidizing element than by forcibly cooling the steel strip so as to have a temperature on the water quenching zone entry side of lower than 105 °C.
The present invention offers a breakthrough in prevention of surface luster degradation in Mg-containing hot-dip Zn plated steel sheets and is therefore used with Mg-containing hot-dip Zn plated steel sheets that experience surface luster degradation. Such an Mg-containing hot-dip Zn plated steel sheet is typically a hot-dip Zn-Al-Mg plated steel sheet exhibiting excellent corrosion resistance and surface appearance obtained by using a hot-dip Zn base bath composed of Al: 4.0 - I S% and Mg: 1.0 - 4.0 % as basic components, plus Ti: O.OOI - 0.1 % and B: 0.001- 0.045 %, and the balance of Zn and unavoidable impurities, and imparting the plating layer with a metallic structure including [primary crystal Al phase] in a matrix of [AUZNZn~Mg ternary eutectic crystal structure] or [primary crystal AI phase], [Zn phase] and/or [ZnZMg phase] in a matrix of [AUZnJZn~Mg ternary eutectic crystal structure]. The metallic structure incluiding [primary crystal A( phase] in a matrix of [AUZn/ZnzMg ternary eutectic crystal structure] is preferably one in which the total amount of [AIIZnIZn~Mg ternary eutectic crystal structure] +
[primary crystal A1 phase] accounts for not less than 80 vof. % of the metallic structure, more preferably for not less than 95 vol.'/° thereof. The balance can consist of [Zn phase] and [ZntMg phase), plus, in some cases, small amounts of [Zn/Zn2Mg binary eutectic crystal]
and/or [Al/ZniMg binary eutectic crystal]. When Si is added, small amounts of [St phase], [Mg~Si phase], [Al/MgiSi binary eutectic crystal] and the like may also be present.
The present invention thus provides a hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in mass %, Al: 4.0 -15 %, Mg: I .0 - 4.0 %, Ti: 0.001- 0.1 °fo B: 0.001- 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon. The plating layer has a metallic structure including [primary crystal Al phase] in a matrix of [AIIZNZn~IvIg ternary eutectic crystal structure] or [primary crystal A1 phase], [Zn phase]
and/or [ZnzMg phase] in a matrix of [AUZnIZn~Mg ternary eutectic crystal structure]. It has a structural characteristic in the point that the one or more readily oxidizing elements are concentrated in the outermost surface layer portion of the plating layer.
The addition amounts, actions and effects of the Al, Mg, Ti, H etc. making up the plating bath remain the same in the plating bath added with at least one readily oxidizing element in accordance with the present invention. Addition of Ti and B is beneficial because these elements act to inhibit generation and growth of Zn"Mgz phase that has and adverse effect on appearance and corrosion resistance when the plating layer is given the aforesaid metallic structure inchuling a ZniMg ternary eutectic crystal structure.
To obtain this effect by adding Ti, B, or Ti-B alloy or compound to the bath, it suPFces to make the addition so that the content in the bath becomes Ti: 0.001 - 0_1 %
and B: 0.001-0.045 %. At higher contents than these, precipitates grow in the plating layer to produce "bumps" (caned as "butsu" in Japanese language) in the plating layer that detract from the surface appearance.
Ai present in the plating layer improves the corrosion resistance of the plated steel sheet and operates to inhibit dross generation during plated steel sheet production. Wt>en the Al content is less than 1.0 mass °l°, the corrosion resistance improving effect is insufficient and the effect of inhibiting generation of Mg oxide system dross is also low. The Al content is preferably made not less than 4.0 mass %.
On the other hand, when the AI content exceeds 15 mass %, pronounced growth of an Fe-A1 alloy layer at the interface between the plating layer and the base steel sheet degrades plating adherence. The A1 content is preferably 4.5 - 13.0 mass %, more preferably 5.0 - 10.0 mass %, and most preferably 5.0 - 7.0 mass %.
Mg present in the plating layer generates a uniform corrosion product on the plating layer surface and, by this, operates to markedly enhance the corrosion resistance of the plated steel sheet. When the Mg content is less than 1.0 °!o, this action of uniformly generating such a corrosion product is insufficient. On the other hand, when the Mg content exceeds 4.0 %, the corrosion resistance improvement effect by Mg saturates and generation of undesirable Mg oxide system dross occurs more readily. The Mg content is therefore defined as 1.0 - 4.0 mass. The Mg content is preferably 1.5 - 4.0 mass %, more preferably 2.0 - 3.5 mass %, most preferably 2.5 - 3.5 mass %.
It was found that the aforesaid surface luster degradation problem also occurs when chemical treatment is applied at the final stage of the Mg-containing hot-dip Zn plated steel sheet production line such as by using the roll water 11 shown at the bottom of FIG. 1, irrespective of whether a chromate coating, a chromate-free conversion coating, an organic resin Flm containing chromium acid, or a silicate film containing chromium acid or other such film is formed. Depending on the production conditions, the phenomenon of a decline in brightness and surface luster degradation atler a few days also occurs (or does not occur) in a plated product having a film produced by chemical treatment, just as it does (or does not) when chemical treatment is not conducted It was found that this emblem can be similarly overcome by controlling the aforesaid strip temperature on the water quenching mne entry side and adding at least one readily oxidizing element to the plating bath in accordance with the present invention.
More speci$cally, also in the case where the steel strip is passed through a chemical treatment zone after being passed through the water quenching zone, the surface luster degradation of the chemically treated Mg-containing hot-dip Zn plated steel sheet - l3-can be inhibited by, as in the foregoing method of producing an Mg-containing hot-dip Zn plated steel sheet, controlling the strip temperature on the water quenching zone entry side to lower than 105 °C or adding 0.002 - 0.05 mass % of a readily oxidizing element to the plating bath.
The present invention thus provides a hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in mass %, Al: a.o- is °i0.
Mg: 1.0 - 4.0 %, Ti: 0.001- 0. I
B: 0.001- 0.045 %, at 1st one readily oxidizing element selected from among ntre earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon, and chemically treating the plating layer.
Example 1 A hot-dip Zn base bath containing about 6 mass % of Al, about 3 mass of Mg, about 0.05 mass % of Ti and about 0.01 mass % of B in zinc was constituted in a facility like that shown in FIG. 1 and an Mg-containing hot-dip Zn plated steel sheets (thickness: 0.8 - l.0 mm) were manufactured to have a plating Layer with a metallic structure including of [primary crystal A1 p6asej, [Zn phase] and [Zn2Mg phase] in a matrix of [AI/ZnJZniMg ternary eutectic crystal structure]. At this time, the strip temperature on the outlet side of the sir-jet cooler 5 was made 335 °C
or lower so as to complete .solidification of the plating layer in the cooler, the cooling conditions and strip running speed were made substantially constant in the air-water cooling nines 6a, 6b, the air cooling zone 14 and the water quenching zone 7, the strip temperature on the water quenching none ? entry side was made 100 °C or lower, and the steel strip was passed through the skin pass mill at about 70 °C or lower. The surface luster of the Mg-containing hot-dip Zn plated steel sheet obtained was excellent and no phenomenon causing degradation thereof was observed.
Steel strips of 1.6 mm or greater thickness were passed under substantially the same conditions as those set out above. Although strip temperature on the water quenching zone 7 entry side rose to around 120 -150 °C, the operation itself was trouble free and Mg-containing hot-dip Zn plated steel sheets having the same excellent surface Iuster were produced. After two yr three days, however, the surface luster of these steel sheets declined slightly, with the brightness L value of some being observed to decrease from 82 just after manufacture to around 75 two days later. 'fhe cooling capacity of the air-water cooling zones 6a, 66 was then increased tv drop the strip temperature on the water quenching zone 7 entry side to lower than 105 °C. As a result, the surface luster degrading phenomenon wes no longer observed.
Also when chromating treatment was conducted, whether or not surface luster degradation occurred again depended on the strip temperature on the water quenching zone 7 entry side. Fmm this it was learned that surface degradation occurs when chromating treatment is conducted in the same way as when it is not.
Example 2 Building on the experience acquired in the preceding Example, the degree of plating layer surface luster degradation was investigated by conducting tests under various conditions. The surface luster was assessed as the brightness (L) measured as the Gab method L value using a spectrophotometer.
First, during production of hot-dip Zn-Al-Mg plated steel sheets under the "Plating conditions" set out below, air water cooling (mist spraying) and water quenching (water stream projection} were conducted under the "Cooling conditions" set out below from the strip temperatiue at completion of plating- layer solidification to about 30 °C. The degrees of sucfacc luster degradation of test pieces taken from the obtained plated steel sheets were evaluated by measuring their L values once just after plating and again after a constant temperature and humidity test in which the test pieces were held in a thecmohygrostat maintained at a temperature of 60 °C and a relative humidity of 90 % for 20 hours starting from just after plating.
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Processed steel strip: Hot-rolled steel strip of 2.0 mm thickness Plating bath composition: AI = 9.0 mass %, Mg = 2.3 mass %, Balance = Zn Plating bath temperature: 430 °C
Coating weight: 90 g/m' Strip naming speed: 80 m/min ~liu~.s~i~ti~o~s (1) Air-water cooling Nozzle: Two-fluid nozzle Fluids: Water (pressure = 12.5 kPa) + Air (pressure = 4.0 kPa) Mist water flow: As shown in Table 1 Mist airflow: As shown in Table 1 Average mist particle diameter: About 50 pcn Strip temperature at start of mist spraying: As shown in Table 1 Strip temperature at end of mist spraying: As shown in Table 1 (2) Water quenching Water stream projector: 7 header rows tech consisting of 10 flat spray nozzles spaced at 150 mm intervals in the direction of strip width Fluid: Water (pressure = 2.5 kgf/cmz) Water flow: As shown in Table 1 Sttip temperature at start of water stream projection: As shown in Table 1 Strip temperature at end of water stream projection: As shown in Table 1 The L values of plated steel sheets obtained under the foregoing conditions at different strip temperatures at start of steam projection (strip temperature on the water quenching entry side) measured just after plating and after the 20-hour constant temperahrre and humidity test are shown in Table 1. The metallic structures of the plating layers were examined by microscopically observing a cross-section of the plating layer of each plated steel sheet. The plating layer of every steel sheet had a metallic structure including [primary crys~l Al phase] in a matrix of [AUZnIZn~Mg ternary eutectic crystal structure], sometimes further including [Zn phase] and [Zn~Mg phase]
(hereinafter called "Zn~Mg-system" metallic structure).
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Example 3 Mg-containing hot..dip Zn plated steel sheets produced under the following conditions using the same cooling conditions after plating layer solidification as in Example 2 were examined for state of surface luster degradation. The results are shown in Table 2.
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The metallic structures of the plating layers were examined by microscopically observing a cross-section of the plating layer of each plated steel sheet. A "ZniMg-system" metallic structure was consistently obtained in every steel sheet.
Fxample 4 Nos. B-2 to B-5 of Example 3 were subjected to chenucal treatrnectt of their water-quenched plating surfaces under the conditions set out below Their brighttresses just after chemical treatment and after a 20-hour constant temperature and humidity test were measured by the method of Example 2. The results are shown in 'Table 3.
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Application method: Spray and wringer roll method Processing solution: Zinchrome 3387N from Nihon Parkecizing Co., Ltd.
(solutioa total chromium concentration: 10 g/L) Chromium coating weight: 10 mg/mZ
Application method: Roll coating method Processing solution: Zinchmme 3387N added with I g/L of zirconium fluoride (solution total chromium concentration: 20 g/L) Chromium coating weight: 40 mglmi Application method: Roll coating method Processing solution: Aqueous solution composed mainly of 50 glL, of magnesium phosphate, 10 g/L of potassium fluorotitanate and 3 g/L of organic acid Metallic component coating weight: 50 mg/mi Coating formed by the following two-step processing Application method: Shower and wringer roll method Processing solution: Zinchrome 3387N (solution total chromium concentration:10 g/L) Chromium coating weight: 10 mg/mi Application method: Roll coating method Organic coating: Urethane resin (thickness: 1.5 Irm) Table 3 ChemicallyChemicalSurface luster F.xampk ~
treated treatment_ L value after 20-h~Ypa tall conditionsL value justconstant (a er after tem nature and chemical humidi test treatment No. B-2 A 81 81 Invention No. t3-4A 81 72 Com 've No. B-3 B 8 t 80 Invention No. B-5 B 8 t 70 Com five No. B-3 C 81 81 Invention No. B-.4C 81 73 Com ive No. B-2 D 81 81 Invention No. 8-5 D 8 l 72 Com arative As can be seen from the results in Table 3, when the strip temperature on the water quenching entry side was 105 °C or higher, the brightness value L decreased with passage of time irrespective of the chemical treatment applied. When the temperature was lower than 105 °C, the brightness just after plating was retained without change.
Example 5 Plating was conducted under the Following plating conditions and cooling conditions with one or more readily oxidizing elements added to the plating bath. Each plating was examined for surface luster degradation. The results are shown in Table 4.
Plating~ndi~i~ns Processed steel strip: Hot-rolled steel strip of 1.6 mm thickness Plating bath composition: As shown in Table 4 Plating bath temperature: 450 °C
Coating weight: 190 glm~
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As shown in FIG. 4, when plated steel sheets like those whose brightness values L fell to around 71 atfer the 20-how constant temperature and humidity test in Examples 2 and 3 were produced in the same manner except for the addition of at least one readily oxidizing element to the plating bath, the decline in brightness L
value was inhibited by the added readily oxidizing element. When the plating surface layer portion of the No. C-7 Mg-containing hot-dip Zn plated steel sheet added with Si was subjected to analysis of its elemental composition by ESCA, it was found that almost all of the Si was concentrated in the outermost surface layer portion of the plating and almost no Si was present in the interior of the plating layer. A comparison of the ESCA analysis results for a plated steel sheet whose brightness L value decreased during the 20-how constant temperature and humidity test (No. C-10) with the results for a plated steel sheet whose brightness L
value did not decrease (No. C-5) showed that Mg tended to be heavily present in the outermost surface layer portion of the plating layer of the former plated steel sheet.
Table 4 includes cases in which the water-quenched plating layer was chemically treated (No. C-12 to No. C-15). The degree of decline in brightness L value differs depending on whether or riot a readily oxidizing element is added and it can be seen that a readily oxidizing element was added, decrease in brightness L value was inhibited.
As explained in the foregoing, the present invention can effectively prevent the phenomenon of surface luster degradation that is peculiar to Mg-containing hot-dip Zn plated steel sheets. It is therefore capable of providing Mg-containing hot-dip Zn plated steel sheet that is good in corrosion resistance and also excellent in luster-retaining property.
HOT-DIP ZN PLATED STEEL SHEET EXCELLENT IN LUSTER RETAINING
PROPERTY AND METHOD OF PRODUCING THE SAME
TECHNICAL FIELD
This invention relates to a technology for preventing surface luster degradation that sometimes occurs during production of hot-dip Zn-AI-Mg plated steel sheet using a continuous hot-dip plating line.
BACKGROUND OF THE ART
JP.Hei-l0-226865A, JP.Hei-l0-306357A, USP No. 6,235,410 (US6,235,410 B 1 ) and USP. No. 6,379,820 (US 6,379,820 B 1 ) owned by the applicant of this application teach that a plated steel sheet having corrosion resistance and surface appearance sufficient to meet the requirements of an industrial product can be obtained manufacturing a hot dip Zn-base plated steel sheet using a hot-dip Zn-AI-Mg-system bath composed of AI: 4.0 -%, Mg: 1.0 - 4.0 %, Ti: 0.002 - 0. I %, B: 0.001 - 0.045 % and the balance of Zn and unavoidable impurities, and imparting to the plating layer a metallic swcture including [primary crystal AI phase) and [Zn single phase) in a matrix of [AIIZn/Zn~Mg ternary eutectic crystal structure). The production conditions for obtaining this metallic structure are set out in ttte published specifications.
1n the course of working with such a relatively high Al- and Mg-content hot dip Zn-base plated steel sheet in ensuing production processes, the inventors experienced that, depending on the production conditions, the surface luster of the plating layer deteriorated within two to three days. This surface luster degradation of the plating layer discolors the aesthetically pleasing plated surface just after plating to a somewhat blackish interference color with passage of time (as quickly as 2 - 3 days but sometimes taking 4 - 7 days). The degree of outermost surface layer discoloration (a kind of blackening) can be quantified by measuring the surface brightness. For example, a plating surface that exhibited a brightness (L value) of around L = 82 just after manufacture degrades to around L = 72 in 7 days. Although this decline in L
value does not degrade the corrosion resistance property of the product and does not impair the physical and chemical qualities of the plated steel sheet, it is undesirable from the point of surface appearance. The fact that the surface luster degradation is not uniform over the plating surface, but takes the form of splotchy discoloration, particularly detracts from the aesthetic appeal.
This degradation of surface luster can be considered to be peculiar to plated steel sheets having relatively high AI and Mg content like the hot-dip Zn-Al-Mg plated steel sheets mentioned above. The degree of oxidation of Mg concentrated in the outermost surface layer of the plating and the oxidized state of the surface layer A1 are most likely complexly involved as causes of the degradation. No reports have been published to date regarding the mechanism of the surface luster degradation occurring in such a hot-dip Zn-Al-Mg plated steel sheet or regarding a method for inhibiting the degradation.
OBJECT OF THE INVENTION
An object of the present invention is therefore to provide means for inhibiting the degradation of surface luster that appears as a problem peculiar to hot-dip Zn-Al-Mg plated steel sheet.
DISCLOSURE OE THE INVENTION
The inventors carried out extensive experimentation and research directed to overcoming the foregoing problem. As a result, we determined that the degradation of the surface luster of hot-dip plated steel sheet is caused by the reaction behavior between the plating layer surface and water during water cooling in the cooling step following plating, that one way to prevent the surface luster degradation is to "control the contact temperature between the plating layer and the water stream" in the water cooling step after plating layer solidification, that, by extension, it is effective to suitably control the'"strip temperature during contact with the water stream," and that it is also effective to stabilize the oxidation state of plating surface layer A1 and Mg by incorporating a small amount of a suitable "readily oxidizing element" in the plating bath. By "strip temperature during contact with the water stream" is meant the strip temperature at the time cooling is conducted while forming a water film on the plating layer surface in the cooling step after completion of plating layer solidification. Specifically, it is the plating layer temperature when a water stream is passed onto the completely solidified plating layer and the plating layer is being cooled with a water film formed on the surface of the plating layer.
In other words, according to the inventors' findings, when steel strip is continuously immersed in and withdrawn from a hot-dip Zn-Al-Mg-system bath of the foregoing description and the steel strip is thereafter continuously passed through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream (while providing onto the plating layer surface an amount of water enabling momentary formation of a water film on the plating layer surface), the aforesaid degradation of plating layer surface luster can be inhibited by controlling the strip temperature on the water quenching zone entry side to lower than 105 °C.
The strip temperature on the water quenching zone entry sib, while depending on the equipment conditions, depends strongly on the sheet thickness. When the strip thickness is great, controlling the strip temperature on the water quenching zone entry side to lower than ! OS °C may not be easy. It was found that in such a case, similar inhibition of surface luster degradation can be achieved without lowering the strip temperature on the water quenching zone entry side to lower than 105 °C
(i.e., with the temperature at 105 °C or higher) by adding to the plating bath a small amount of an element that has a very powerful affinity for oxygen (that is a readily oxidizing element) and that has a stabilizing effect on AI oxides. Such elements include, for example, the rare earth elements, Y, Zr and Si. In actual practice, it sutFtces to add about 0.002 - 0.05 mass % of the readily oxidizing element.
Thus, the present invention provides a method of producing a hot-dip Zn plated steel sheet excellent in luster-retaining property comprising a step of continuously immersing and withdrawing steel strip intolfrom a hot-dip Zn base bath containing Al: 4.0 -15 mass % and Mg: 1.0 - 4.0 mass %, thereby forming a plating layer thereon, and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, degradation of the plating layer luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to lower than 105 °C.
The hat.~lip Zn base bath is preferably composed of, in mass %, Al: 4.0 -15 %, Mg: 1.0 -4.0 %, Ti: 0.001 - 0.1 %, B: 0.001 - 0.045 % and the balance of Zn and unavoidable impurities.
The present invention further provides a method of producing a hot-dip Zn plated steel sheet excellent in luster-retaining property comprising a step of continuously immersing and withdrawing steel strip intolfrom a hot-dip Zn base bath containing AI: 4.0 - 15 mass % and Mg: 1.0 - 4.0 mass % and added with 0.002 - 0.05 mass % of at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si, thereby forming a plating layer thereon, and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, degradation of the plating layer surface luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to not lower then 105 °C and not higher than 300 °C. The hot-dip Zn base bath is preferably composed of, in mass %, Al: 4.0 - 15 ~/°, Mg: 1.0 - 4.0 %, Ti: 0.001- 0.1.%, H: 0.001- 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities.
The present invention further provides, as a hot-dip Zn plated steel sheet obtained the foregoing methods, a hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in %
Al: 4.0 -15 % arid Mg: 1.0 - 4.0 %, optionally, Ti: 0.001- 0.1 % and B: 0.001- 0.045 %, preferably, at least one c~eadily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05'/0, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon. The plating layer has a metallic structure inching [primary crystal A1 phase] in a matrix of [AUZn/Zn~Mg ternary eutectic crystal structure] or [primary crystal Al phase], [Zn phase]
and/or [Zn~lVig phase] in a matrix of [AIIZn/ZniMg ternary eutectic crystal structure].
' BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a line diagram schematically illustrating a facility for producing Mg-containing hot-dip Zn plated steel sheet according to the pc~esent invention.
PREFERRED EMBODIMENTS OF THE INVENTION
Generally in this specification, the term "steel strip" is used when explaining the hot-dip plating tine and the term "steel sheet" ;s used when explaining the product. However, the steel strip and steel sheet have the same characteristics.
FIG. 1 schematically illustrates a facility used to produce a hot dip Zn-base plated steel sheet. A steel strip 2 passed through a furnace 1 to be maintained at a prescribed temperature is continuously fed into a plating bath 3. Upon exiting the plating bath 3, the steel strip passes through a wiping nozzle 4 that regulates its coating weight and then through an air jet cooler 5. The plating layer is completely solidified during passage through the air jet cooler 5. The strip next passes through air-water cooling zones 6a, 6b and an air cooling zone 14, any of which may be operated alone or in combination with the others, or not be operated, and then through a water quenching zone 7. It is then temper-rolled in a skin pass mill 8, passed thmugh a tension leveller 9, passed through an inspection step and taken up on a tension reel I0. When chromating or other such chemical treatment is conducted, the steel strip exiting the tension lever 9 is treated in a roll coater I 1, passed through a drying zone 12 and an air cooling zone 13, and taken up on a tension reel 10a.
As explained earlier, when producing a hot-dip Zn-Al-Mg plated steel sheet containing relatively large amounts of A1 and Mg (hereinafter called "Mg-containing hot-dip Zn plated steel sheet', appropriate control of the cooling rate up to complete plating Iayer solidification and of the solidification completion position is essential from the aspect of surface property. For this, the strip feeding speed must be strictly controlled and the strip temperature at the time of passage through the air jet cooler 5 needs to be exactly controlled in accordance with the sheet thickness. Next, so as to enable suitable temper rolling at the skin pass mill 8, the strip temperature at the skin pass entry side needs to be adjusted to a prescribed level (e.g., not more than 70 °C) by cooling conducted at the sir-water cooling zones 6 (and the air cooling zone 14) and/or the water quenching zone 7.
The cooling load at these cooling zones vanes with the strip conning speed and the sheet thickness. Generally, water or a water solution is sprayed at the air-water cooling zones, air is jetted at the air jet cooling zone, and, at the water quenching zone, a water stream - 7 .
adequate for momentarily forming a water film on the plating layer surface is supplied.
Compared with the first mentioned cooling stages, the latter mentioned water quenching zone can achieve a faster cooling rate owing to the contact of the water stream with the plating layer surface. Efficient cooling operation can therefore be conducted at the water quenching zone irrespective of variation in cooling load. Although water or a water solution is sprayed together with an air stream at air-water cooling zone 6, not enough water is supplied to form a water film on the plating layer surface. The cooling is therefore chiefly the result of latent heat extraction by evaporation. This is a different form of heat removal from that by contact with a water stream as in the water quenching tone and therefore differs in cooling rate.
It was found that the luster-retaining property of the plating surface differs depending on strip temperature on the water quenching mne entry side. When the temperature is 105 °C or higher, surface luster degradation readily occurs. While the reason for this is not certain, the inventors concluded that the causes involve such factors as that the reactivity of the plating layer surface is enhanced by the occurrence of a kind of boiling phenomenon when the strip temperature is l 00 °C or higher upon entering the water quenching zone and that the behavior of AI under atmospheric pressure in the presence of water differs above and below about 110 °C, i.e., Ah03 Hi0 (or AIOOH) compound is stable above this temperature while Al=Oj~3H=0 (or AI(OH)3) compound is stable Ixlow this temperature, so that the Al compound formed on the plating layer surface in the water quenching mne differs depending on the entry side steel strip temperature.
In an Mg-containing hot-dip Zn plated steel sheet of the foregoing type having a metallic structure including [primary crystal A1 phase], (Zn phase]
and/or [Zn~lv(g phase] in a matrix of [AUZn/Zn~Mg ternary eutectic crystal structure], the outermost surface of the ternary eutectic crystal structure is changed into a readily oxidizing form by the aforesaid chemical reaction and this is believed to be why surface luster degradation that produces a change in brightness occurs within two or three days after plating.
_g_ At any rate, the inventors discovered that, as demonstrated by the Examples set out later, the surface luster degradation of an Mg-containing hot-dip Zn plated steel sheet can be substantially prevented by regulating the temperature of the steel strip entering the water quenching zone to lower than 105 °C.1n this case, the cooling operation before entry into to the water quenching zone needs to be conduMed not by supplying enough water to the completely solidified plating surface to form a water film that produces quenching, as is done in the water quenching zone, but by a mild cooling operation such as by air-water cooling (mist spraying) or air cooling (e.g.
air jet cooling).
This is because regulation of the steel strip temperature entering the water quenching zone to lower than 105 °C would be meaningless if a quenching operation that forms a water film as is done in the water quenching zone should be conducted before the steel strip enters the water quenching zone. Depending on the sheet thickness and the strip running speed, the strip temperature on the water quenching zone entry side can be regulated to lower-than 105 °C even by air-water cooling.
When the sheet thickness is large, however, it may sometimes be impossible to regulate the strip temperature on the water quenching zone entry side to lower than 105 °C. Although a sufficient amount of cooling in the air-water cooling regions can be achieved even when sheet thickness is large by reducing the strip running speed, this is inadvisable because it leads to problems in solidification point control and lowers productivity. Even when the strip temperature on the water quenching zone entry side is 105 °C or higher, however, surface luster degradation can be effectively inhibited, as is demonstrated by the Examples set out later, by making present at the just completely solidified plating surface an appropriate amount of a readily oxidizing element that hss a very powerful amity for oxygen and a stabilizing effect on At oxides, such as a rare earth element, Y, Zr or Si. In actual practice, it suffices to add about 0.002 -0.05 mass a/o of the readily oxidizing element. Although other elements that exhibit an effect similar to the rare earth elements, Y, Zr and Si may exist, none has yet been identified.
These readily oxidizing elements have a property of concentrating at the outermost surface layer portion of the plating layer during the solidification process of the plating layer of the Mg-containing hot-dip Zn plated steel sheet, or even after solidification.
These elements can therefore reach a relatively high concentration at the outermost surface layer portion even when added to the plating bath in only a small amount. This is thought to enable them to inhibit surface reactions in the water quenching zone which adversely affect the surface luster-maintaining property. When these readily oxidizing elements are added to the plating bath at less than 0.002 %, however, they do not manifest the inhibiting effect. They must therefore be added so as to make their content in the plating bath composition not less than 0.002 mass %. On the other hand, amounts added in excess have poor solubility in the plating bath and even if dissolved only saturate the surface luster degradation inhibiting effect because the elements simply precipitate in excess near the grain boundaries in the plating surface layer portion. The amount added is therefore such that the content in the plating bath becomes not more than 0.10 mass %, in some cases not more than 0,08 mass %, preferably 0.05 mass %, more preferably 0.03 mass %.
The surface luster degradation preventing effect produced by addidan of one or mute reaudily oxidizing elements is acts most effectively when, as explained in the foregoing, the strip temperature on the water quenching zonc entry side is 105 °C or higher.
Even when the strip temperature on the water quenching zone entry side is tower than 105 °C, however, one or more readily oxidizing elements can be added to the plating both to stay an the safe side.
In the case where the strip temperature on the water quenching zone entry side is 105 °C or higher, it should preferably be controlled to not higher than 300 °C
because at higher than 300 °C the cooling load in the water quenching zone becomes so large as to prevent sufficient lowering of the temperature on the skin pass entry side.
In an ordinary production line, if the strip thickness is less than 1.6 mm, the strip temperature on the water quenching zone entry side can be relatively easily made - (0 -lower than 105 °C so as to ensure good luster-retaining property When the strip thickness is 1.6 mm or greater, it is, from the aspect of actual operation, better to ensure lusoer-retaining property by addition of a readily oxidizing element than by forcibly cooling the steel strip so as to have a temperature on the water quenching zone entry side of lower than 105 °C.
The present invention offers a breakthrough in prevention of surface luster degradation in Mg-containing hot-dip Zn plated steel sheets and is therefore used with Mg-containing hot-dip Zn plated steel sheets that experience surface luster degradation. Such an Mg-containing hot-dip Zn plated steel sheet is typically a hot-dip Zn-Al-Mg plated steel sheet exhibiting excellent corrosion resistance and surface appearance obtained by using a hot-dip Zn base bath composed of Al: 4.0 - I S% and Mg: 1.0 - 4.0 % as basic components, plus Ti: O.OOI - 0.1 % and B: 0.001- 0.045 %, and the balance of Zn and unavoidable impurities, and imparting the plating layer with a metallic structure including [primary crystal Al phase] in a matrix of [AUZNZn~Mg ternary eutectic crystal structure] or [primary crystal AI phase], [Zn phase] and/or [ZnZMg phase] in a matrix of [AUZnJZn~Mg ternary eutectic crystal structure]. The metallic structure incluiding [primary crystal A( phase] in a matrix of [AUZn/ZnzMg ternary eutectic crystal structure] is preferably one in which the total amount of [AIIZnIZn~Mg ternary eutectic crystal structure] +
[primary crystal A1 phase] accounts for not less than 80 vof. % of the metallic structure, more preferably for not less than 95 vol.'/° thereof. The balance can consist of [Zn phase] and [ZntMg phase), plus, in some cases, small amounts of [Zn/Zn2Mg binary eutectic crystal]
and/or [Al/ZniMg binary eutectic crystal]. When Si is added, small amounts of [St phase], [Mg~Si phase], [Al/MgiSi binary eutectic crystal] and the like may also be present.
The present invention thus provides a hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in mass %, Al: 4.0 -15 %, Mg: I .0 - 4.0 %, Ti: 0.001- 0.1 °fo B: 0.001- 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon. The plating layer has a metallic structure including [primary crystal Al phase] in a matrix of [AIIZNZn~IvIg ternary eutectic crystal structure] or [primary crystal A1 phase], [Zn phase]
and/or [ZnzMg phase] in a matrix of [AUZnIZn~Mg ternary eutectic crystal structure]. It has a structural characteristic in the point that the one or more readily oxidizing elements are concentrated in the outermost surface layer portion of the plating layer.
The addition amounts, actions and effects of the Al, Mg, Ti, H etc. making up the plating bath remain the same in the plating bath added with at least one readily oxidizing element in accordance with the present invention. Addition of Ti and B is beneficial because these elements act to inhibit generation and growth of Zn"Mgz phase that has and adverse effect on appearance and corrosion resistance when the plating layer is given the aforesaid metallic structure inchuling a ZniMg ternary eutectic crystal structure.
To obtain this effect by adding Ti, B, or Ti-B alloy or compound to the bath, it suPFces to make the addition so that the content in the bath becomes Ti: 0.001 - 0_1 %
and B: 0.001-0.045 %. At higher contents than these, precipitates grow in the plating layer to produce "bumps" (caned as "butsu" in Japanese language) in the plating layer that detract from the surface appearance.
Ai present in the plating layer improves the corrosion resistance of the plated steel sheet and operates to inhibit dross generation during plated steel sheet production. Wt>en the Al content is less than 1.0 mass °l°, the corrosion resistance improving effect is insufficient and the effect of inhibiting generation of Mg oxide system dross is also low. The Al content is preferably made not less than 4.0 mass %.
On the other hand, when the AI content exceeds 15 mass %, pronounced growth of an Fe-A1 alloy layer at the interface between the plating layer and the base steel sheet degrades plating adherence. The A1 content is preferably 4.5 - 13.0 mass %, more preferably 5.0 - 10.0 mass %, and most preferably 5.0 - 7.0 mass %.
Mg present in the plating layer generates a uniform corrosion product on the plating layer surface and, by this, operates to markedly enhance the corrosion resistance of the plated steel sheet. When the Mg content is less than 1.0 °!o, this action of uniformly generating such a corrosion product is insufficient. On the other hand, when the Mg content exceeds 4.0 %, the corrosion resistance improvement effect by Mg saturates and generation of undesirable Mg oxide system dross occurs more readily. The Mg content is therefore defined as 1.0 - 4.0 mass. The Mg content is preferably 1.5 - 4.0 mass %, more preferably 2.0 - 3.5 mass %, most preferably 2.5 - 3.5 mass %.
It was found that the aforesaid surface luster degradation problem also occurs when chemical treatment is applied at the final stage of the Mg-containing hot-dip Zn plated steel sheet production line such as by using the roll water 11 shown at the bottom of FIG. 1, irrespective of whether a chromate coating, a chromate-free conversion coating, an organic resin Flm containing chromium acid, or a silicate film containing chromium acid or other such film is formed. Depending on the production conditions, the phenomenon of a decline in brightness and surface luster degradation atler a few days also occurs (or does not occur) in a plated product having a film produced by chemical treatment, just as it does (or does not) when chemical treatment is not conducted It was found that this emblem can be similarly overcome by controlling the aforesaid strip temperature on the water quenching mne entry side and adding at least one readily oxidizing element to the plating bath in accordance with the present invention.
More speci$cally, also in the case where the steel strip is passed through a chemical treatment zone after being passed through the water quenching zone, the surface luster degradation of the chemically treated Mg-containing hot-dip Zn plated steel sheet - l3-can be inhibited by, as in the foregoing method of producing an Mg-containing hot-dip Zn plated steel sheet, controlling the strip temperature on the water quenching zone entry side to lower than 105 °C or adding 0.002 - 0.05 mass % of a readily oxidizing element to the plating bath.
The present invention thus provides a hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in mass %, Al: a.o- is °i0.
Mg: 1.0 - 4.0 %, Ti: 0.001- 0. I
B: 0.001- 0.045 %, at 1st one readily oxidizing element selected from among ntre earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon, and chemically treating the plating layer.
Example 1 A hot-dip Zn base bath containing about 6 mass % of Al, about 3 mass of Mg, about 0.05 mass % of Ti and about 0.01 mass % of B in zinc was constituted in a facility like that shown in FIG. 1 and an Mg-containing hot-dip Zn plated steel sheets (thickness: 0.8 - l.0 mm) were manufactured to have a plating Layer with a metallic structure including of [primary crystal A1 p6asej, [Zn phase] and [Zn2Mg phase] in a matrix of [AI/ZnJZniMg ternary eutectic crystal structure]. At this time, the strip temperature on the outlet side of the sir-jet cooler 5 was made 335 °C
or lower so as to complete .solidification of the plating layer in the cooler, the cooling conditions and strip running speed were made substantially constant in the air-water cooling nines 6a, 6b, the air cooling zone 14 and the water quenching zone 7, the strip temperature on the water quenching none ? entry side was made 100 °C or lower, and the steel strip was passed through the skin pass mill at about 70 °C or lower. The surface luster of the Mg-containing hot-dip Zn plated steel sheet obtained was excellent and no phenomenon causing degradation thereof was observed.
Steel strips of 1.6 mm or greater thickness were passed under substantially the same conditions as those set out above. Although strip temperature on the water quenching zone 7 entry side rose to around 120 -150 °C, the operation itself was trouble free and Mg-containing hot-dip Zn plated steel sheets having the same excellent surface Iuster were produced. After two yr three days, however, the surface luster of these steel sheets declined slightly, with the brightness L value of some being observed to decrease from 82 just after manufacture to around 75 two days later. 'fhe cooling capacity of the air-water cooling zones 6a, 66 was then increased tv drop the strip temperature on the water quenching zone 7 entry side to lower than 105 °C. As a result, the surface luster degrading phenomenon wes no longer observed.
Also when chromating treatment was conducted, whether or not surface luster degradation occurred again depended on the strip temperature on the water quenching zone 7 entry side. Fmm this it was learned that surface degradation occurs when chromating treatment is conducted in the same way as when it is not.
Example 2 Building on the experience acquired in the preceding Example, the degree of plating layer surface luster degradation was investigated by conducting tests under various conditions. The surface luster was assessed as the brightness (L) measured as the Gab method L value using a spectrophotometer.
First, during production of hot-dip Zn-Al-Mg plated steel sheets under the "Plating conditions" set out below, air water cooling (mist spraying) and water quenching (water stream projection} were conducted under the "Cooling conditions" set out below from the strip temperatiue at completion of plating- layer solidification to about 30 °C. The degrees of sucfacc luster degradation of test pieces taken from the obtained plated steel sheets were evaluated by measuring their L values once just after plating and again after a constant temperature and humidity test in which the test pieces were held in a thecmohygrostat maintained at a temperature of 60 °C and a relative humidity of 90 % for 20 hours starting from just after plating.
~nditlo~
Processed steel strip: Hot-rolled steel strip of 2.0 mm thickness Plating bath composition: AI = 9.0 mass %, Mg = 2.3 mass %, Balance = Zn Plating bath temperature: 430 °C
Coating weight: 90 g/m' Strip naming speed: 80 m/min ~liu~.s~i~ti~o~s (1) Air-water cooling Nozzle: Two-fluid nozzle Fluids: Water (pressure = 12.5 kPa) + Air (pressure = 4.0 kPa) Mist water flow: As shown in Table 1 Mist airflow: As shown in Table 1 Average mist particle diameter: About 50 pcn Strip temperature at start of mist spraying: As shown in Table 1 Strip temperature at end of mist spraying: As shown in Table 1 (2) Water quenching Water stream projector: 7 header rows tech consisting of 10 flat spray nozzles spaced at 150 mm intervals in the direction of strip width Fluid: Water (pressure = 2.5 kgf/cmz) Water flow: As shown in Table 1 Sttip temperature at start of water stream projection: As shown in Table 1 Strip temperature at end of water stream projection: As shown in Table 1 The L values of plated steel sheets obtained under the foregoing conditions at different strip temperatures at start of steam projection (strip temperature on the water quenching entry side) measured just after plating and after the 20-hour constant temperahrre and humidity test are shown in Table 1. The metallic structures of the plating layers were examined by microscopically observing a cross-section of the plating layer of each plated steel sheet. The plating layer of every steel sheet had a metallic structure including [primary crys~l Al phase] in a matrix of [AUZnIZn~Mg ternary eutectic crystal structure], sometimes further including [Zn phase] and [Zn~Mg phase]
(hereinafter called "Zn~Mg-system" metallic structure).
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Example 3 Mg-containing hot..dip Zn plated steel sheets produced under the following conditions using the same cooling conditions after plating layer solidification as in Example 2 were examined for state of surface luster degradation. The results are shown in Table 2.
Pla~ngs~~diti~
Processed steel strip: Hot-rolled steel strip of 3.2 mm thickness Plating bath composition: Al = 6.3 mass %, Mg = 3.2 mass %, Ti = 0.008 mass %, B =
0.002 mass %, Balance = Zn Plating bath temperature: 390 °C
Coating weight: 120 g/mi Strip running speed: Varied as shown in Table 2 ~a~lin~c~diti~ns (1) Gas cooling (Cooling with air-jet cooler only) Nozzle: Plato-like nozzle with slit of 5 mm width Gas: Air (pressure = 4 kPa) Airflow: As shown in Table 2 Strip temperature at start of air cooling: As shown in Table 2 Strip temperature at end of air cooling: As shown in Table 2 (2) Water quenching f9 -Water stream projector: 7 header rows each consisting of 10 flat spray nozzles spaced at 150 mm intervals in the direction of strip width Fluid: Water (pressure = 2.2 kgf/cm~) Water flow: As shown in Table 2 Strip temperature at start of water stream projection: As shown in Table 2 Strip temperature at end of water stream projection: As shown in Table 2 arn pp o z a a c cc "
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f7n m =~ a o ' < ' ' _ e n n As can be seen From the results in Table 2, in this Example as in Example 2, when the strip tanperature on the water quenching entry side was higher than 105 °C, the tendency for the brightness L value to decrease became stronger as the temperature increased, but when the temperature was lower than 105 °C, the brightness just after plating remained the same even after the 20-hour constant temperature and humidity test.
The metallic structures of the plating layers were examined by microscopically observing a cross-section of the plating layer of each plated steel sheet. A "ZniMg-system" metallic structure was consistently obtained in every steel sheet.
Fxample 4 Nos. B-2 to B-5 of Example 3 were subjected to chenucal treatrnectt of their water-quenched plating surfaces under the conditions set out below Their brighttresses just after chemical treatment and after a 20-hour constant temperature and humidity test were measured by the method of Example 2. The results are shown in 'Table 3.
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Application method: Spray and wringer roll method Processing solution: Zinchrome 3387N from Nihon Parkecizing Co., Ltd.
(solutioa total chromium concentration: 10 g/L) Chromium coating weight: 10 mg/mZ
Application method: Roll coating method Processing solution: Zinchmme 3387N added with I g/L of zirconium fluoride (solution total chromium concentration: 20 g/L) Chromium coating weight: 40 mglmi Application method: Roll coating method Processing solution: Aqueous solution composed mainly of 50 glL, of magnesium phosphate, 10 g/L of potassium fluorotitanate and 3 g/L of organic acid Metallic component coating weight: 50 mg/mi Coating formed by the following two-step processing Application method: Shower and wringer roll method Processing solution: Zinchrome 3387N (solution total chromium concentration:10 g/L) Chromium coating weight: 10 mg/mi Application method: Roll coating method Organic coating: Urethane resin (thickness: 1.5 Irm) Table 3 ChemicallyChemicalSurface luster F.xampk ~
treated treatment_ L value after 20-h~Ypa tall conditionsL value justconstant (a er after tem nature and chemical humidi test treatment No. B-2 A 81 81 Invention No. t3-4A 81 72 Com 've No. B-3 B 8 t 80 Invention No. B-5 B 8 t 70 Com five No. B-3 C 81 81 Invention No. B-.4C 81 73 Com ive No. B-2 D 81 81 Invention No. 8-5 D 8 l 72 Com arative As can be seen from the results in Table 3, when the strip temperature on the water quenching entry side was 105 °C or higher, the brightness value L decreased with passage of time irrespective of the chemical treatment applied. When the temperature was lower than 105 °C, the brightness just after plating was retained without change.
Example 5 Plating was conducted under the Following plating conditions and cooling conditions with one or more readily oxidizing elements added to the plating bath. Each plating was examined for surface luster degradation. The results are shown in Table 4.
Plating~ndi~i~ns Processed steel strip: Hot-rolled steel strip of 1.6 mm thickness Plating bath composition: As shown in Table 4 Plating bath temperature: 450 °C
Coating weight: 190 glm~
Strip running speed: 60 -120 m/min ~~nulin~s~ditit~
( 1 ) Air-water cooling Nozzle: Two-fluid nozzle Fluids: Water (pressure =1.0 - 3.5 kgf/cmZ) + Air (pressure = 2.5 - 5.0 kgf/cm=) Mist water flow: 0 - 8 m'1h Mist airflow: 0 - 600 m'/min Average mist particle diameter: 10 - 30 pro (2) Gas cooling Nozzle: Plate-like nozzle with slit of 5 mm width Gas: Air (pressure = 4 kPa) Airflow: 0 - 3500 m'/m (3) Water quenching Water stream projector: 7 header rows each consisting of 10 flat spray nozzles spaced at 150 mm intervals in the direction of strip width Fluid: Water (pressure = 3.0 kgf/cm~) Water flow: 180 m'!h Strip temperature at start of water steam projection: As shown in Table 4 n~ n nn ~~n ~n ~~ nn~ ~ ~~ x 00i Q~ireJaWN~ ~~ 0ev ~UJvW N..fi l!~O~ ? inOvWOvrrV1InOvJ OOv1~~0 0DW
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As shown in FIG. 4, when plated steel sheets like those whose brightness values L fell to around 71 atfer the 20-how constant temperature and humidity test in Examples 2 and 3 were produced in the same manner except for the addition of at least one readily oxidizing element to the plating bath, the decline in brightness L
value was inhibited by the added readily oxidizing element. When the plating surface layer portion of the No. C-7 Mg-containing hot-dip Zn plated steel sheet added with Si was subjected to analysis of its elemental composition by ESCA, it was found that almost all of the Si was concentrated in the outermost surface layer portion of the plating and almost no Si was present in the interior of the plating layer. A comparison of the ESCA analysis results for a plated steel sheet whose brightness L value decreased during the 20-how constant temperature and humidity test (No. C-10) with the results for a plated steel sheet whose brightness L
value did not decrease (No. C-5) showed that Mg tended to be heavily present in the outermost surface layer portion of the plating layer of the former plated steel sheet.
Table 4 includes cases in which the water-quenched plating layer was chemically treated (No. C-12 to No. C-15). The degree of decline in brightness L value differs depending on whether or riot a readily oxidizing element is added and it can be seen that a readily oxidizing element was added, decrease in brightness L value was inhibited.
As explained in the foregoing, the present invention can effectively prevent the phenomenon of surface luster degradation that is peculiar to Mg-containing hot-dip Zn plated steel sheets. It is therefore capable of providing Mg-containing hot-dip Zn plated steel sheet that is good in corrosion resistance and also excellent in luster-retaining property.
Claims (13)
1. A method of producing a hot-dip Zn plated steel sheet excellent in luster-retaining property comprising:
a step of continuously immersing and withdrawing steel strip into/from a hot-dip Zn base bath containing Al: 4.0 - 15 mass % and Mg: 1.0 - 4.0 mass %, thereby forming a plating layer thereon; and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, wherein degradation of the plating layer luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to lower than 105 °C.
a step of continuously immersing and withdrawing steel strip into/from a hot-dip Zn base bath containing Al: 4.0 - 15 mass % and Mg: 1.0 - 4.0 mass %, thereby forming a plating layer thereon; and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, wherein degradation of the plating layer luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to lower than 105 °C.
2. A method of producing a hot-dip Zn plated steel sheet excellent in luster-retaining property comprising:
a step of continuously immersing and withdrawing steel strip into/from a hot-dip Zn base bath containing, in mass %, Al: 4.0 - 15 %, Mg: 1.0-4.0 %, Ti: 0.001 - 0.1 %, B: 0.001 - 0.045 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon; and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, wherein degradation of the plating layer luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to lower than 105 °C.
a step of continuously immersing and withdrawing steel strip into/from a hot-dip Zn base bath containing, in mass %, Al: 4.0 - 15 %, Mg: 1.0-4.0 %, Ti: 0.001 - 0.1 %, B: 0.001 - 0.045 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon; and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, wherein degradation of the plating layer luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to lower than 105 °C.
3. A method of producing a hot-dip Zn plated steel sheet excellent in luster-retaining property comprising:
a step of continuously immersing and withdrawing steel strip into/from a hot-dip Zn base bath containing Al: 4.0 - 15 mass % and Mg: 1.0 - 4.0 mass % and added with 0.002 - 0.05 mass % of at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si, thereby forming a plating layer thereon; and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, wherein degradation of the plating layer surface luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to not lower than 105 °C.
a step of continuously immersing and withdrawing steel strip into/from a hot-dip Zn base bath containing Al: 4.0 - 15 mass % and Mg: 1.0 - 4.0 mass % and added with 0.002 - 0.05 mass % of at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si, thereby forming a plating layer thereon; and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, wherein degradation of the plating layer surface luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to not lower than 105 °C.
4. A method of producing a hot-dip Zn plated steel sheet excellent in luster-retaining property comprising:
a step of continuously immersing and withdrawing steel strip into/from a hot-dip Zn base bath containing, in mass %, Al: 4.0 - 15 %, Mg: 1.0-4.0 %, Ti: 0.001 - 0.1 %, B: 0.001 - 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon; and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, wherein degradation of the plating layer luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to not lower than 105 °C and not higher than higher than 300 °C.
a step of continuously immersing and withdrawing steel strip into/from a hot-dip Zn base bath containing, in mass %, Al: 4.0 - 15 %, Mg: 1.0-4.0 %, Ti: 0.001 - 0.1 %, B: 0.001 - 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon; and a step of thereafter continuously passing the steel strip through a water quenching zone that effects cooling while bringing the completely solidified plating layer surface into contact with a water stream, wherein degradation of the plating layer luster being inhibited at this time by controlling strip temperature on the water quenching zone entry side to not lower than 105 °C and not higher than higher than 300 °C.
5. A method of producing a hot-dip Zn plated steel sheet excellent in luster-retaining property according to any one of claims 1 to 4, further comprising a step of passing the steel strip passed through the water quenching zone through a chemical treatment zone.
6. A hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in mass %, Al: 4.0 - 15 %, Mg: 1.0 - 4.0 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon.
7. A hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in mass %, Al: 4.0 - 15 %, Mg: 1.0 - 4.0%, Ti: 0.001- 0.1 %
B: 0.001 - 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon.
B: 0.001 - 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon.
8. A hot-dip Zn plated steel sheet excellent in luster-retaining property according to claim 6 or 7, wherein the readily oxidizing element is concentrated in the outermost surface layer portion of the plating layer.
9. A hot-dip Zn plated steel sheet excellent in luster-retaining property according to any one of claims 6 to 8, wherein the plating layer has a metallic structure including primary crystal Al phase in a matrix of Al/Zn/Zn2Mg ternary eutectic crystal structure.
10. A hot-dip Zn plated steel sheet excellent in luster-retaining property according to any one of claims 6 to 8, wherein the plating layer has a metallic structure including primary crystal Al phase and at least one phase of Zn phase and Zn2Mg phase in a matrix of Al/Zn/Zn2Mg ternary eutectic crystal structure.
11. A hot-dip Zn plated steel sheet excellent in luster-retaining property according to any one of claims 6 to 8, wherein the plating layer has a metallic structure including at least one phase of Zn phase and Zn2Mg phase in a matrix of Al/Zn/Zn2Mg ternary eutectic crystal structure.
12. A hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in mass %, Al: 4.0 - 15%, Mg: 1.0 - 4.0 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon, and chemically treating the plating layer.
13. A hot-dip Zn plated steel sheet excellent in luster-retaining property obtained by hot-dip plating a steel strip using a hot-dip plating bath comprising, in mass %, Al: 4.0 - 15%, Mg: 1.0 - 4.0 %, Ti: 0.001 - 0.1 %
B: 0.001 - 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon, and chemically treating the plating layer.
B: 0.001 - 0.045 %, at least one readily oxidizing element selected from among rare earth elements, Y, Zr and Si: 0.002 - 0.05 %, and the balance of Zn and unavoidable impurities, thereby forming a plating layer thereon, and chemically treating the plating layer.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2002/007485 WO2004009863A1 (en) | 2002-07-24 | 2002-07-24 | Zinc-base hot dip galvanized steel sheet excellent in retention of gloss |
Publications (2)
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CA2444460A1 CA2444460A1 (en) | 2004-01-24 |
CA2444460C true CA2444460C (en) | 2008-01-22 |
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CA002444460A Expired - Lifetime CA2444460C (en) | 2002-07-24 | 2002-07-24 | Hot-dip zn plated steel sheet excellent in luster-retaining property and method of producing the same |
Country Status (9)
Country | Link |
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EP (1) | EP1524326B1 (en) |
CN (1) | CN1276990C (en) |
AT (1) | ATE484605T1 (en) |
AU (1) | AU2002323927B2 (en) |
CA (1) | CA2444460C (en) |
DE (1) | DE60238001D1 (en) |
ES (1) | ES2350921T3 (en) |
NZ (1) | NZ528816A (en) |
WO (1) | WO2004009863A1 (en) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100666693B1 (en) | 2004-11-23 | 2007-01-11 | 삼성전자주식회사 | Monolithic duplexer |
CN102330043B (en) * | 2011-08-03 | 2013-03-13 | 马鞍山鼎泰稀土新材料股份有限公司 | Steel wire hot dipping rare earth zinc alloy and hot dipping method |
CN103361588B (en) * | 2012-03-30 | 2016-04-06 | 鞍钢股份有限公司 | Low aluminium low magnesium system zinc-aluminum-magnesium Coated Steel production method and Coated Steel thereof |
JP5097305B1 (en) * | 2012-04-25 | 2012-12-12 | 日新製鋼株式会社 | Black plated steel plate |
WO2013160566A1 (en) | 2012-04-25 | 2013-10-31 | Arcelormittal Investigacion Y Desarrollo, S.L. | Method for producing a metal sheet having oiled zn-al-mg coatings, and corresponding metal sheet |
US20160168658A1 (en) | 2012-10-17 | 2016-06-16 | Bluescope Steel Limited | Method of producing metal-coated steel strip |
TWI653362B (en) * | 2012-10-17 | 2019-03-11 | 澳大利亞商布魯史寇普鋼鐵有限公司 | Method of producing metal-coated steel strip |
NZ706324A (en) | 2012-10-18 | 2019-02-22 | Bluescope Steel Ltd | Method of producing metal coated steel strip |
EP2824213A1 (en) * | 2013-07-12 | 2015-01-14 | Voestalpine Stahl GmbH | Method for improving adherence to a steel sheet with a protective coating |
CA2935047C (en) | 2013-12-20 | 2021-01-05 | Arcelormittal | Process for producing a znalmg-coated metal sheet with optimized wiping and corresponding metal sheet |
KR101767788B1 (en) | 2015-12-24 | 2017-08-14 | 주식회사 포스코 | Plating steel material having excellent friction resistance and white rust resistance and method for manufacturing same |
CN108779543A (en) * | 2016-03-31 | 2018-11-09 | 日新制钢株式会社 | The manufacturing method of hot-dip aluminizing steel wire |
KR102031466B1 (en) | 2017-12-26 | 2019-10-11 | 주식회사 포스코 | Zinc alloy coated steel having excellent surface property and corrosion resistance, and method for manufacturing the same |
KR102425278B1 (en) * | 2018-05-16 | 2022-07-27 | 닛폰세이테츠 가부시키가이샤 | plated steel |
CN108977695B (en) * | 2018-09-30 | 2020-12-01 | 济南大学 | Titanium and antimony-containing hot-dip galvanized aluminum magnesium alloy and preparation method thereof |
TWI691615B (en) * | 2019-04-10 | 2020-04-21 | 中國鋼鐵股份有限公司 | Zinc-coated steel sheet and method of forming the same |
CN113025937B (en) * | 2021-02-07 | 2023-03-17 | 首钢集团有限公司 | Hot-dip galvanized steel plate and preparation method thereof |
CN112941417A (en) * | 2021-03-03 | 2021-06-11 | 靖江新舟合金材料有限公司 | Alloy coated steel plate and production method thereof |
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CN113604765B (en) * | 2021-10-09 | 2022-01-04 | 天津市弘仁金属材料有限公司 | Steel strip hot dipping method |
CN115261703A (en) * | 2022-06-08 | 2022-11-01 | 日照宝华新材料有限公司 | Manufacturing method of high-corrosion-resistance steel plate for photovoltaic support |
Family Cites Families (9)
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---|---|---|---|---|
JP2754126B2 (en) * | 1992-11-26 | 1998-05-20 | 新日本製鐵株式会社 | Hot-dip Zn-Al plated steel sheet with excellent appearance, blackening resistance over time and corrosion resistance |
JP3148542B2 (en) * | 1995-01-11 | 2001-03-19 | 新日本製鐵株式会社 | Hot-dip galvanized steel sheet with excellent glare resistance |
JPH10265926A (en) * | 1997-03-25 | 1998-10-06 | Nisshin Steel Co Ltd | Production of hot dip zn-al-mg coated steel strip excellent in corrosion resistance and appearance |
JP3888784B2 (en) * | 1998-09-21 | 2007-03-07 | 日新製鋼株式会社 | Edge wrinkle prevention method for hot-dip Zn-based plated steel sheet |
JP2001295015A (en) * | 2000-02-09 | 2001-10-26 | Nisshin Steel Co Ltd | HOT DIP HIGH Al-CONTAINING Zn-Al-Mg BASE METAL COATED STEEL SHEET |
JP2002080952A (en) * | 2000-06-29 | 2002-03-22 | Nisshin Steel Co Ltd | Home building material excellent in corrosion resistance, and home building member |
JP2002146504A (en) * | 2000-08-22 | 2002-05-22 | Nisshin Steel Co Ltd | Material for electrical equipment and member for electrical equipment having excellent corrosion resistance and whisker resistance |
JP2002187234A (en) * | 2000-12-21 | 2002-07-02 | Nisshin Steel Co Ltd | Non-chromium coated steel plate having excellent corrosion resistance |
JP4064634B2 (en) * | 2001-02-02 | 2008-03-19 | 日新製鋼株式会社 | Hot-dip Zn-based plated steel sheet with good gloss retention and method for producing the same |
-
2002
- 2002-07-24 NZ NZ528816A patent/NZ528816A/en not_active IP Right Cessation
- 2002-07-24 WO PCT/JP2002/007485 patent/WO2004009863A1/en active IP Right Grant
- 2002-07-24 AU AU2002323927A patent/AU2002323927B2/en not_active Expired
- 2002-07-24 DE DE60238001T patent/DE60238001D1/en not_active Expired - Lifetime
- 2002-07-24 CA CA002444460A patent/CA2444460C/en not_active Expired - Lifetime
- 2002-07-24 EP EP02755638A patent/EP1524326B1/en not_active Expired - Lifetime
- 2002-07-24 CN CN02808369.5A patent/CN1276990C/en not_active Expired - Lifetime
- 2002-07-24 ES ES02755638T patent/ES2350921T3/en not_active Expired - Lifetime
- 2002-07-24 AT AT02755638T patent/ATE484605T1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE60238001D1 (en) | 2010-11-25 |
EP1524326B1 (en) | 2010-10-13 |
CN1276990C (en) | 2006-09-27 |
AU2002323927B2 (en) | 2005-08-25 |
AU2002323927A1 (en) | 2004-02-09 |
EP1524326A4 (en) | 2006-09-13 |
WO2004009863A1 (en) | 2004-01-29 |
ES2350921T3 (en) | 2011-01-28 |
EP1524326A1 (en) | 2005-04-20 |
CA2444460A1 (en) | 2004-01-24 |
NZ528816A (en) | 2005-10-28 |
CN1503853A (en) | 2004-06-09 |
ATE484605T1 (en) | 2010-10-15 |
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