TW201812039A - Titanium composite material and method for manufacturing same, and package - Google Patents
Titanium composite material and method for manufacturing same, and package Download PDFInfo
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- TW201812039A TW201812039A TW106111206A TW106111206A TW201812039A TW 201812039 A TW201812039 A TW 201812039A TW 106111206 A TW106111206 A TW 106111206A TW 106111206 A TW106111206 A TW 106111206A TW 201812039 A TW201812039 A TW 201812039A
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- 239000010936 titanium Substances 0.000 title claims abstract description 387
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 title claims abstract description 377
- 229910052719 titanium Inorganic materials 0.000 title claims abstract description 369
- 239000002131 composite material Substances 0.000 title claims abstract description 110
- 238000004519 manufacturing process Methods 0.000 title claims description 44
- 238000000034 method Methods 0.000 title claims description 30
- 150000003609 titanium compounds Chemical class 0.000 claims abstract description 84
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 34
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 32
- 239000000203 mixture Substances 0.000 claims abstract description 29
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 27
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 26
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910001069 Ti alloy Inorganic materials 0.000 claims abstract description 21
- 150000004767 nitrides Chemical class 0.000 claims abstract description 21
- 239000000126 substance Substances 0.000 claims abstract description 20
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000001301 oxygen Substances 0.000 claims abstract description 17
- 239000000463 material Substances 0.000 claims description 142
- 239000010410 layer Substances 0.000 claims description 96
- 239000000843 powder Substances 0.000 claims description 66
- 238000012856 packing Methods 0.000 claims description 54
- 238000012545 processing Methods 0.000 claims description 36
- 239000002344 surface layer Substances 0.000 claims description 36
- 239000012535 impurity Substances 0.000 claims description 22
- 238000005096 rolling process Methods 0.000 claims description 19
- 229910052742 iron Inorganic materials 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 239000005022 packaging material Substances 0.000 claims description 16
- 239000000956 alloy Substances 0.000 claims description 11
- 150000001247 metal acetylides Chemical class 0.000 claims description 10
- 238000011049 filling Methods 0.000 claims description 9
- 238000005482 strain hardening Methods 0.000 claims description 8
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- 239000002245 particle Substances 0.000 description 36
- 238000009792 diffusion process Methods 0.000 description 26
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 25
- 238000003466 welding Methods 0.000 description 18
- 229940125936 compound 42 Drugs 0.000 description 16
- 238000010438 heat treatment Methods 0.000 description 16
- 239000000470 constituent Substances 0.000 description 14
- 238000005098 hot rolling Methods 0.000 description 13
- 239000011162 core material Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 239000000945 filler Substances 0.000 description 10
- 238000005336 cracking Methods 0.000 description 9
- 238000005520 cutting process Methods 0.000 description 9
- 238000005242 forging Methods 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 229910052802 copper Inorganic materials 0.000 description 8
- 239000010949 copper Substances 0.000 description 8
- 238000004806 packaging method and process Methods 0.000 description 8
- 238000009864 tensile test Methods 0.000 description 8
- 229910010413 TiO 2 Inorganic materials 0.000 description 7
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 7
- 238000010586 diagram Methods 0.000 description 7
- 230000003287 optical effect Effects 0.000 description 7
- 239000011800 void material Substances 0.000 description 7
- 229910003460 diamond Inorganic materials 0.000 description 6
- 239000010432 diamond Substances 0.000 description 6
- 210000002257 embryonic structure Anatomy 0.000 description 6
- 229910000975 Carbon steel Inorganic materials 0.000 description 5
- 239000010962 carbon steel Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 150000003608 titanium Chemical class 0.000 description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 238000000137 annealing Methods 0.000 description 3
- 238000005097 cold rolling Methods 0.000 description 3
- 210000001161 mammalian embryo Anatomy 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 238000005554 pickling Methods 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 238000005245 sintering Methods 0.000 description 3
- 229910052718 tin Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 238000004453 electron probe microanalysis Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229910000883 Ti6Al4V Inorganic materials 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- -1 compound compound Chemical class 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000008570 general process Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000001192 hot extrusion Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 238000006902 nitrogenation reaction Methods 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000000304 warm extrusion Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21B—ROLLING OF METAL
- B21B1/00—Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations
- B21B1/02—Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations for rolling heavy work, e.g. ingots, slabs, blooms, or billets, in which the cross-sectional form is unimportant ; Rolling combined with forging or pressing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21B—ROLLING OF METAL
- B21B3/00—Rolling materials of special alloys so far as the composition of the alloy requires or permits special rolling methods or sequences ; Rolling of aluminium, copper, zinc or other non-ferrous metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F7/00—Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression
- B22F7/02—Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression of composite layers
- B22F7/04—Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression of composite layers with one or more layers not made from powder, e.g. made from solid metal
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C14/00—Alloys based on titanium
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Composite Materials (AREA)
- Manufacturing & Machinery (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Metal Rolling (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
本發明有關一種鈦複合材及其製造方法、以及捆包體。 The invention relates to a titanium composite material, a manufacturing method thereof, and a packing body.
鈦材為耐蝕性優異之金屬材料,因此已被利用於使用海水之熱交換器或各種化學工廠等。又,由於其密度比碳鋼為小,且比強度(每單位重量之強度)優異,因此亦多量使用於航空器之機體。又,藉由於汽車等之陸上輸送機器中使用鈦材,陸上輸送機器自體變得輕量,可期待燃料費之降低。 Titanium is a metal material with excellent corrosion resistance, so it has been used in heat exchangers using seawater or various chemical plants. In addition, since its density is smaller than that of carbon steel and its specific strength (strength per unit weight) is excellent, it is also used in a large amount in aircraft bodies. In addition, since a titanium material is used in land transportation equipment such as automobiles, the land transportation equipment itself becomes lightweight, and a reduction in fuel cost can be expected.
然而,鈦材與鋼材相比係經由複雜且非常多的步驟所製造。其代表性製造步驟係如以下所例示:(1)製鍊步驟:將作為原料之氧化鈦氯化而形成四氯化鈦之後,以鎂或鈉還原,藉而製造海綿狀(塊狀)之金屬鈦(以下,稱為「海綿鈦」)之步驟;(2)熔解步驟:將海綿鈦壓製成形而形成為電極,並以真空電弧熔解爐予以熔解而製造鑄錠之步驟;(3)鍛造步驟:將鑄錠作熱間鍛造而製造扁胚(熱軋素材)或小胚(熱擠壓或熱軋等之素材)等之步驟; (4)熱加工步驟:將扁胚或小胚加熱並作熱輥軋或擠壓而製造板或圓棒等之步驟;(5)冷加工步驟:將板或圓棒進一步作冷軋加工或擠壓而製造薄板或圓棒、線等之步驟。 However, compared with steel, titanium is produced through complicated and very many steps. The representative manufacturing steps are as exemplified below: (1) Chain-making step: chlorinating titanium oxide as a raw material to form titanium tetrachloride, and then reducing it with magnesium or sodium to produce a sponge-like (lumpy) Steps of metal titanium (hereinafter referred to as "sponge titanium"); (2) melting step: a step of pressing titanium sponge to form an electrode and melting it in a vacuum arc melting furnace to produce an ingot; (3) forging Steps: Steps of making ingots as hot forging to produce flat embryos (hot-rolled materials) or small embryos (materials such as hot extrusion or hot rolling); (4) Hot processing steps: heating the flat embryos or small embryos It is also used for the steps of hot rolling or extrusion to manufacture plates or round bars, etc .; (5) Cold working step: the step of cold rolling or pressing the plates or round bars to manufacture thin plates or round bars, wires, etc.
鈦材由於係以如此多的步驟製造,故而非常高價。是以,鈦材幾乎無法適用於汽車等之陸上輸送機器。因此,為了促進鈦材之利用,有必要提高其製造步驟之生產性。為了應對此一課題,已有將鈦材之製造步驟簡單化之配合機制 Titanium is very expensive because it is manufactured in so many steps. Therefore, titanium materials can hardly be applied to land transportation equipment such as automobiles. Therefore, in order to promote the use of titanium, it is necessary to improve the productivity of its manufacturing steps. In order to cope with this problem, there is a matching mechanism that simplifies the manufacturing steps of titanium
專利文獻1中,揭示有一種將含有鈦粉、黏結劑、可塑劑、溶劑之組成物成形為薄板狀,並予乾燥、燒結、壓密及再燒結而製造鈦薄板之方法。根據此一方法,可省略上述熔解步驟,鍛造步驟、熱軋步驟及冷軋步驟。 Patent Document 1 discloses a method for manufacturing a titanium sheet by molding a composition containing titanium powder, a binder, a plasticizer, and a solvent into a thin plate shape, and drying, sintering, compacting, and re-sintering. According to this method, the above-mentioned melting step, forging step, hot rolling step, and cold rolling step can be omitted.
專利文獻2中,揭示有一種於鈦合金粉中添加銅粉、鉻粉或是鐵粉,予以封入碳鋼製之包封內,並予加熱作熱擠壓而製造鈦合金圓棒之方法。根據此一方法,可省略上述熔解步驟及鍛造步驟,因此可降低製造成本。 Patent Document 2 discloses a method for manufacturing a titanium alloy round rod by adding copper powder, chromium powder, or iron powder to a titanium alloy powder, encapsulating the same in a carbon steel envelope, and heating and extruding it. According to this method, since the melting step and the forging step described above can be omitted, the manufacturing cost can be reduced.
專利文獻3中,揭示一種將海綿鈦粉填充於銅製包封中,並予加熱於700℃以下實施溫熱擠壓加工,而製造圓棒之方法。根據此一方法,可省略上述熔解步驟及鍛造步驟,因此可降低製造成本。 Patent Document 3 discloses a method for manufacturing a round rod by filling sponge titanium powder in a copper package and preheating it at 700 ° C. or lower and performing warm extrusion processing. According to this method, since the melting step and the forging step described above can be omitted, the manufacturing cost can be reduced.
又,先前既知之疊板輥軋,係一種將加工性不良之鈦合金等之芯材以加工性良好之價廉的碳鋼等之被覆材被覆再予熱軋之方法。例如,於芯材之表面塗布剝離 劑後,至少將其上下2面以被覆材被覆,或是除上下面以外將4周面亦以被覆材被覆,並將接縫熔接而製作密閉被覆箱,而後將其內部抽真空並密閉,然後進行熱軋。 In addition, the previously known laminated sheet rolling method is a method of coating a core material such as a titanium alloy with poor workability with a coating material such as carbon steel with good processability and then hot rolling. For example, after applying a release agent to the surface of the core material, at least two sides of the core material are covered with a covering material, or four peripheral surfaces are covered with a covering material in addition to the upper and lower surfaces, and the seam is welded to make a closed covering box. Then, the inside was evacuated and sealed, and then hot rolled.
有關疊板輥軋,專利文獻4中揭示有一種密閉被覆箱之組裝方法;專利文獻5中,揭示有一種設置10-3torr(約0.133Pa)以上之真空度並將被覆材密封(包裝)而製造密閉被覆箱之方法;再者,專利文獻6中,揭示有一種以碳鋼(被覆材)被覆,並於10-2torr(約1.33Pa)以下之真空下利用高能量密度熔接而密封(包裝),據以製造密閉被覆箱之方法。 Regarding lamination rolling, Patent Document 4 discloses a method for assembling a closed coating box; Patent Document 5 discloses a method of setting a vacuum degree of 10 -3 torr (about 0.133Pa) and sealing (packaging) the coating material. And a method for manufacturing a closed coating box; Furthermore, Patent Document 6 discloses a method of coating with carbon steel (coating material) and sealing by high energy density welding under a vacuum of 10 -2 torr (approximately 1.33Pa). (Packaging), a method for manufacturing a closed covered box.
根據此等疊板輥軋,由於係將被輥軋材之芯材以被覆材被覆並熱軋,因此芯材之表面不會直接接觸冷態媒體(大氣或輥),而可抑制芯材之溫度降低,因此即使是加工性不佳之芯材也能夠製造薄板。 According to these laminated rolls, since the core material of the rolled material is covered with a covering material and hot-rolled, the surface of the core material does not directly contact the cold medium (air or roller), and the core material can be suppressed. The temperature is reduced, so that even a core material with poor workability can produce a thin plate.
作為被覆材,係使用與芯材不同之材質且加工性良好的價廉之碳鋼等。被覆材在熱軋後變得不需要,因此為了使其易於自芯材分離,芯材之表面塗布有剝離劑。 As the covering material, an inexpensive carbon steel or the like is used which is a material different from the core material and has good workability. Since the covering material becomes unnecessary after hot rolling, in order to make it easy to separate from the core material, the surface of the core material is coated with a release agent.
[專利文獻1]日本特開2011-042828號公報 [Patent Document 1] Japanese Patent Laid-Open No. 2011-042828
[專利文獻2]日本特開2014-019945號公報 [Patent Document 2] Japanese Patent Laid-Open No. 2014-019945
[專利文獻3]日本特開2001-131609號公報 [Patent Document 3] Japanese Patent Laid-Open No. 2001-131609
[專利文獻4]日本特開昭63-207401號公報 [Patent Document 4] Japanese Patent Laid-Open No. 63-207401
[專利文獻5]日本特開平09-136102號公報 [Patent Document 5] Japanese Patent Laid-Open No. 09-136102
[專利文獻6]日本特開平11-057810號公報 [Patent Document 6] Japanese Patent Laid-Open No. 11-057810
根據專利文獻1所揭示之方法,由於將高價之鈦粉(平均粒徑4~200μm)作為原料使用,且需要燒結或壓密等之許多步驟,因之所獲得之鈦薄板非常高價,未能促進鈦材之利用。 According to the method disclosed in Patent Document 1, high-priced titanium powder (average particle diameter of 4 to 200 μm) is used as a raw material, and many steps such as sintering or compacting are required. Therefore, the obtained titanium sheet is very expensive and cannot be obtained. Promote the use of titanium.
根據專利文獻2所揭示之方法,由於係將高價之鈦粉合金作為原料使用,因此所獲得之鈦合金圓棒高價,未能促進鈦材之利用。尚且,加熱時由於海綿鈦粉會被氧化,因此所得之圓棒其表層與內部含有氧化鈦,與一般步驟所製造之圓棒相比,有外觀變色及拉伸特性劣化等之問題。 According to the method disclosed in Patent Document 2, because a titanium powder alloy with a high price is used as a raw material, the obtained titanium alloy round rod is expensive and fails to promote the use of a titanium material. In addition, since the sponge titanium powder is oxidized during heating, the surface layer and the inside of the obtained round rod contain titanium oxide. Compared with the round rod produced in the general process, there are problems such as appearance discoloration and deterioration in tensile properties.
根據專利文獻3所揭示之方法,加熱時由於海綿鈦粉會被氧化,因此所得之圓棒其表層與內部含有氧化鈦,與一般步驟所製造之圓棒相比,有外觀變色及拉伸特性劣化等之問題。 According to the method disclosed in Patent Document 3, since the sponge titanium powder is oxidized during heating, the surface layer and the inside of the obtained round rod contain titanium oxide. Compared with the round rod manufactured by ordinary steps, the round rod has discoloration and tensile properties. Problems such as deterioration.
再者,根據專利文獻4~6所揭示之方法,由於如疊板輥軋般,在輥軋後將被覆材剝離廢棄,因此製造成本變得較一般之步驟還高,且所獲得之鈦材為高成本此一事實並未改變。 In addition, according to the methods disclosed in Patent Documents 4 to 6, since the covering material is peeled off and discarded after being rolled, such as lamination rolling, the manufacturing cost becomes higher than ordinary steps, and the obtained titanium material The fact that it is high cost has not changed.
因此,鈦材並未達於可適用於汽車等之陸上輸送機器的地步。 Therefore, the titanium material has not reached the point where it can be applied to land transportation equipment such as automobiles.
本發明係有鑑如此般之實情開發而成者,其目的係在以低成本提供鈦板或鈦圓棒等之鈦材。 The present invention was developed based on such facts, and its purpose is to provide titanium materials such as titanium plates or titanium rods at a low cost.
本發明人等,為了解決上述課題,銳意研討可於省略熔解步驟及鍛造步驟下製造鈦材之手段,獲得以下所列般之敘述般之知識與見解(A)~(F),終而完成本發明。 In order to solve the above-mentioned problems, the present inventors devotedly studied the means for manufacturing titanium materials without omitting the melting step and the forging step, and obtained the narrative general knowledge and opinions (A) ~ (F) listed below, and finally completed this invention.
(A)並非高價之鈦粉或海綿鈦粉般之粉末,而是將不定形且為海綿狀(塊狀)之海綿鈦作為原料使用。海綿狀之海綿鈦,自先前起即有製造,可較價廉地獲得。此外,海綿鈦於製鍊步驟中其鐵、氯等之主要雜質被除去,因此即使自海綿鈦直接製造鈦材,化學組成上並無問題。又,無法成為製品之下腳料等之鈦材(以下,稱為「鈦邊角料」)可較價廉地獲得。惟鈦邊角料為不定形,因此無法直接加工製造鈦材。 (A) It is not a high-priced titanium powder or a sponge-like titanium powder, but an irregular and sponge-like (lumpy) sponge titanium is used as a raw material. Sponge-like sponge titanium has been manufactured since earlier and can be obtained at a lower cost. In addition, the main impurities such as iron and chlorine of the sponge titanium are removed in the chain-making step, so even if the titanium material is directly produced from the sponge titanium, there is no problem in chemical composition. In addition, a titanium material (hereinafter, referred to as a "titanium scrap") which cannot be used as an undercut of a product can be obtained relatively inexpensively. However, the titanium scrap is irregular, so it cannot be processed and manufactured directly.
(B)若為於使用工業用純鈦材或鈦合金材製作之容器(以下,稱為「捆包材」)中,收容海綿鈦等之填充材並予密閉成之鈦捆包體,則於熱加工時,可抑制表面破裂或鱗片狀等之表面缺陷的發生。特別是藉由將填充材之化學組成設成與純鈦材同種,則並無如先前之疊板輥軋般在輥軋後將被覆材剝離廢棄的必要,可將鈦捆包材即使在 熱加工後亦能原狀作為鈦複合材(製品)之一部分有效地利用。 (B) If the container is made of a pure titanium material or titanium alloy material for industrial use (hereinafter referred to as a "packaging material"), and it is a titanium packaging body that contains a filling material such as sponge titanium and is hermetically sealed, During hot working, it is possible to suppress the occurrence of surface cracks such as surface cracks and scale-like defects. In particular, by setting the chemical composition of the filler material to be the same as that of the pure titanium material, there is no need to peel and discard the coating material after rolling, as in the previous laminated sheet rolling. After processing, it can be effectively used as a part of the titanium composite material (product).
(C)於熱加工前進行加熱時,為了使海綿鈦等之填充材不氧化,且於熱加工時使填充材間或填充材與捆包材間之空隙易於減少,重要的是將捆包材之內壓事先儘量減壓。 (C) In order to prevent the filling materials such as sponge titanium from being oxidized when heating before hot working, and to easily reduce the gap between the filling materials or between the filling material and the packing material during hot processing, it is important to pack The internal pressure of the material should be reduced as much as possible in advance.
(D)作為收容於捆包材之填充材,藉由與海綿鈦等之鈦材一起,又填充選自碳、碳化物、氮化物及氧化物之1種以上的粉末,而可提高鈦複合材之抗拉強度。 (D) As a packing material contained in a packing material, titanium compound such as sponge titanium is filled with one or more powders selected from carbon, carbide, nitride, and oxide to improve titanium compounding. Tensile strength of wood.
(E)亦即,藉由於工業用純鈦之韌材(伸展材)即鈦捆包材之內部,填充及封入海綿鈦、及可提高鈦複合材之抗拉強度的選自碳、碳化物、氮化物及氧化物之1種以上的粉末,並將內部減壓形成為鈦捆包體,對於此一鈦捆包體進行熱加工,並因應必要進一步又進行冷加工而形成為鈦複合材,使得熱加工前鈦塊之集合即鈦捆包體,在熱加工後成為整體經壓縮成形一體化之鈦複合材(三層之包層材)。 (E) That is, because the tough material (stretch material) of industrial pure titanium, that is, the titanium packing material, is filled and sealed with sponge titanium, and it is selected from carbon and carbide to improve the tensile strength of the titanium composite material. Powder of at least one of nitride, oxide, and oxide, and the internal pressure is reduced to form a titanium bundle body. This titanium bundle body is hot-processed and further cold-processed as necessary to form a titanium composite material. The result is that the assembly of titanium blocks before thermal processing, that is, the titanium packing body, becomes a titanium composite material (three-layer clad material) that is integrally compressed and integrated after thermal processing.
(F)鈦複合材係只有內層部含有可提高鈦複合材之抗拉強度的選自碳化物、氮化物及氧化物之1種以上的鈦化合物之鈦的壓縮成形體,而表層部為工業用純鈦或是鈦合金材之韌材,因此具有優異之加工性與高抗拉強度,而且可不經由先前之熔解步驟與鍛造步驟即行製造,故而可大幅降低製造成本。 (F) The titanium composite material is a compression-molded body in which only the inner layer portion contains titanium containing one or more titanium compounds selected from carbides, nitrides, and oxides, which can improve the tensile strength of the titanium composite material, and the surface layer portion is Industrial pure titanium or a tough material of titanium alloy material has excellent workability and high tensile strength, and can be manufactured without the previous melting step and forging step, so the manufacturing cost can be greatly reduced.
本發明係如以下所列般之敘述。 The invention is described as listed below.
(1)一種鈦複合材,係具有內層部及被覆上述內層部之表層部的鈦複合材,上述表層部包含屬於JIS1種~4種之任一種的化學組成之工業用純鈦材或鈦合金材,上述內層部,係於鈦中分散有選自碳化物、氮化物及氧化物之1種以上的鈦化合物,且具有上述碳化物之周圍為碳、上述氮化物之周圍為氮、上述氧化物之周圍為氧而分別擴散之部分,以面積率計具有大於0%且30%以下之空隙。 (1) A titanium composite material is a titanium composite material having an inner layer portion and a surface layer portion covering the inner layer portion, and the surface layer portion includes an industrial pure titanium material having a chemical composition of any one of JIS 1 to 4 or Titanium alloy material, the inner layer part is a titanium compound in which one or more titanium compounds selected from carbides, nitrides, and oxides are dispersed, and the periphery of the carbides is carbon, and the periphery of the nitrides is nitrogen. The portions surrounding the above oxides are oxygen and diffuse separately, and have an area ratio of greater than 0% and less than 30%.
(2)如上述(1)之鈦複合材,其中上述內層部之碳、氮及氧之平均含量的合計為0.05~2.0質量%,且上述鈦化合物係以沿著輥軋方向排列之條狀化合物集合體分散於鈦材中。 (2) The titanium composite material according to the above (1), wherein the total of the average content of carbon, nitrogen, and oxygen in the inner layer portion is 0.05 to 2.0% by mass, and the titanium compound is a strip arranged along the rolling direction The compound-like aggregate is dispersed in a titanium material.
(3)如上述(1)或(2)之鈦複合材,其中上述工業用純鈦材之化學組成,以質量%計為:C:0.08%以下、H:0.013%以下、O:0.4%以下、N:0.05%以下、Fe:0.5%以下、其餘部分:Ti及雜質。 (3) The titanium composite material as described in (1) or (2) above, wherein the chemical composition of the above-mentioned industrial pure titanium material is expressed as mass%: C: 0.08% or less, H: 0.013% or less, O: 0.4% Below, N: 0.05% or less, Fe: 0.5% or less, and the rest: Ti and impurities.
(4)一種鈦複合材之製造方法,其係藉由於包含屬於JIS1~4種之任一種的工業用純鈦材或鈦合金材之鈦捆包材中,填充選自海綿鈦、鈦塊體及鈦邊角料之1種 以上、及選自碳、碳化物、氮化物及氧化物之1種以上的粉末並封入,且將其內部減壓為10Pa以下而形成為鈦捆包體,再對上述鈦捆包體進行熱加工。 (4) A method for manufacturing a titanium composite material, which is filled with a material selected from the group consisting of sponge titanium and titanium blocks by using a titanium packing material including industrial pure titanium material or titanium alloy material belonging to any of JIS1 to 4 And titanium scraps, and at least one powder selected from carbon, carbides, nitrides, and oxides are sealed, and the internal pressure is reduced to 10 Pa or less to form a titanium bundle. The titanium package is hot-worked.
(5)如上述(4)之鈦複合材之製造方法,其中進行上述熱加工後再進行冷加工。 (5) The method for producing a titanium composite material according to the above (4), wherein the hot working is performed before the cold working.
(6)一種熱加工用的捆包體,係具備:包含屬於JIS1~4種之任一種的工業用純鈦材或鈦合金材之鈦捆包材、及填充於上述鈦捆包材內部之填充材的捆包體; 上述填充材具有:選自海綿鈦、鈦塊體及鈦邊角料之1種以上、及選自碳、碳化物、氮化物及氧化物之1種以上之粉末,上述內部之壓力為10Pa以下。 (6) A packaging body for thermal processing, comprising: a titanium packaging material including industrial pure titanium materials or titanium alloy materials belonging to any one of JIS1 to 4; and a titanium packaging material filled inside the titanium packaging material. Packing body of filling material; The filling material includes: one or more powders selected from sponge titanium, titanium block and titanium scrap, and one or more powders selected from carbon, carbide, nitride, and oxide; The pressure is 10 Pa or less.
本發明之鈦複合材,抗拉強度、楊氏模數等之機械特性優異,而且可不經由熔解步驟及鍛造步驟等製造,因此可大幅降低製造成本。又,本發明之鈦複合材,可在不進行鑄錠之表層與底面多量之缺陷部之切削除去、鍛造後之表面破裂或形狀不良的前後端部(切料頭)之除去等,即在不進行將多量之鈦素材切削除去或切斷除去下製造,因此可大幅提升製造良率,就此點亦可使製造成本大幅降低。 The titanium composite material of the present invention is excellent in mechanical properties such as tensile strength and Young's modulus, and can be manufactured without a melting step and a forging step, so the manufacturing cost can be greatly reduced. In addition, the titanium composite material of the present invention can be removed without cutting and removing a large number of defective portions on the surface layer and the bottom surface of the ingot, and the front and rear end portions (cutting heads) of the surface after cracking or poor shape after forging. Manufacturing is not performed by cutting or removing a large amount of titanium material, so the manufacturing yield can be greatly improved, and the manufacturing cost can be greatly reduced at this point.
1‧‧‧鈦複合材 1‧‧‧ titanium composite
2‧‧‧表層部 2‧‧‧ Surface Department
3‧‧‧表層部 3‧‧‧ Surface Department
4‧‧‧內層部 4‧‧‧ Inner Department
41‧‧‧鈦 41‧‧‧ Titanium
42‧‧‧鈦化合物 42‧‧‧ titanium compounds
42a‧‧‧條狀化合物集合體 42a‧‧‧ Strip Compound
43‧‧‧空隙 43‧‧‧Gap
5‧‧‧鈦捆包體 5‧‧‧ titanium package
6‧‧‧鈦捆包材 6‧‧‧Titanium packing material
7‧‧‧海綿鈦 7‧‧‧ titanium sponge
8‧‧‧鈦化合物等之粉末 8‧‧‧ titanium powder
9‧‧‧空隙 9‧‧‧ gap
10‧‧‧塊體 10‧‧‧ block
11‧‧‧熔接部 11‧‧‧ Welding Department
12‧‧‧鈦捆包體 12‧‧‧ titanium package
第1圖係表示本發明鈦複合材之構成之一例的 說明圖。 Fig. 1 is an explanatory diagram showing an example of the constitution of the titanium composite material of the present invention.
第2圖係示意性表示條狀化合物集合體42a的圖。 Fig. 2 is a view schematically showing a strip-shaped compound aggregate 42a.
第3圖係表示於鈦複合材1之與長度方向(輥軋方向)及厚度方向平行的截面(厚度截面)中,1個粒子之厚度方向的距離與其周圍的元素濃度分布之概念的圖。 FIG. 3 is a diagram showing the concept of the distance between the thickness direction of one particle and the element concentration distribution around the titanium composite material 1 in a section (thickness section) parallel to the longitudinal direction (rolling direction) and the thickness direction.
第4圖係表示本發明鈦複合材之熱加工用素材即鈦捆包體之構成之一例的說明圖。 FIG. 4 is an explanatory diagram showing an example of the structure of a titanium bundle which is a material for thermal processing of a titanium composite material according to the present invention.
第5圖係表示鈦塊體之構成之一例的說明圖。 Fig. 5 is an explanatory diagram showing an example of the structure of a titanium block.
第6圖係表示本發明鈦捆包體之其他構成之一例的說明圖。 Fig. 6 is an explanatory diagram showing another example of the structure of the titanium packing body of the present invention.
第7圖係Ti-0.1%N板的截面微組織照片。 Figure 7 is a photograph of the cross-section microstructure of a Ti-0.1% N plate.
將本發明鈦複合材及鈦捆包體,參照附圖說明之。又,以降之說明中,有關化學組成之「%」如無特別異議均是指「質量%」。 The titanium composite material and the titanium packing body of the present invention will be described with reference to the drawings. In addition, the "%" in the chemical composition means "mass%" without special objection.
第1圖係表示本發明鈦複合材1之構成之一例的說明圖。 FIG. 1 is an explanatory diagram showing an example of the configuration of the titanium composite material 1 of the present invention.
如第1圖所示,鈦複合材1具備:表層部2、3與內層部4。以下,針對各層說明之。 As shown in FIG. 1, the titanium composite material 1 includes surface layer portions 2 and 3 and an inner layer portion 4. Hereinafter, each layer will be described.
作為形成表層部2、3之工業用純鈦材,可使用屬於JIS1~4種之任一種的化學組成之工業用純鈦材。例如,表層部2、3具有:C:0.08%以下、H:0.013%以下、O:0.4%以下、N:0.05%以下、Fe:0.5%以下、其餘部分Ti及雜質的化學組成。 As the industrial pure titanium material forming the surface layer portions 2 and 3, an industrial pure titanium material having a chemical composition of any one of JIS 1 to 4 can be used. For example, the surface layer portions 2 and 3 have C: 0.08% or less, H: 0.013% or less, O: 0.4% or less, N: 0.05% or less, Fe: 0.5% or less, and the chemical composition of the remaining portions of Ti and impurities.
又,上述之JIS1種~4種,係採JISH4600:2012所規定者。JIS1種係指具有:C:0.08%以下、H:0.013%以下、O:0.15%以下、N:0.03%以下、Fe:0.20%以下、其餘部分Ti及雜質之組成。JIS2種係指具有:C:0.08%以下、H:0.013%以下、O:0.20%以下、N:0.03%以下、Fe:0.25%以下、其餘部分Ti及雜質之組成。JIS3種係指具有:C:0.08%以下、H:0.014%以下、O:0.30%以下、N:0.05%以下、Fe:0.30%以下、其餘部分Ti及雜質之組成。JIS4種係指具有:C:0.08%以下、H:0.013%以下、O:0.40%以下、N:0.05%以下、Fe:0.50%以下、其餘部分Ti及雜質之組成。 In addition, the above-mentioned JIS types 1 to 4 are those specified in JISH4600: 2012. JIS1 refers to the composition of: C: 0.08% or less, H: 0.013% or less, O: 0.15% or less, N: 0.03% or less, Fe: 0.20% or less, the rest of Ti and impurities. JIS2 refers to the composition of: C: 0.08% or less, H: 0.013% or less, O: 0.20% or less, N: 0.03% or less, Fe: 0.25% or less, the rest of Ti and impurities. JIS3 refers to the composition of: C: 0.08% or less, H: 0.014% or less, O: 0.30% or less, N: 0.05% or less, Fe: 0.30% or less, the rest of Ti and impurities. JIS4 refers to the composition of: C: 0.08% or less, H: 0.013% or less, O: 0.40% or less, N: 0.05% or less, Fe: 0.50% or less, the rest of Ti and impurities.
另一方面,作為形成表層部2、3之鈦合金材,可使用α型鈦合金、α+β型鈦合金、或是β型鈦合金。 On the other hand, as the titanium alloy material forming the surface layer portions 2 and 3, an α-type titanium alloy, an α + β-type titanium alloy, or a β-type titanium alloy can be used.
作為α型鈦合金,例如有Ti-0.06%Pd、Ti-0.2Pd、Ti-0.02Pd-0.05Mm(此處,Mm係指混合稀土金屬)、Ti-0.5Ni-0.05Ru、Ti-0.5Cu、Ti-1.0Cu、Ti-1.0Cu-0.5Nb、Ti-1.0Cu-1.0Sn-0.3Si-0.25Nb、Ti-0.5Al-0.45Si、Ti-0.9Al-0.35Si、Ti-3Al-2.5V、Ti-5Al-2.5Sn、Ti-6Al- 2Sn-4Zr-2Mo、Ti-6Al-2.75Sn-4Zr-0.4Mo-0.45Si等。 Examples of the α-type titanium alloy include Ti-0.06% Pd, Ti-0.2Pd, Ti-0.02Pd-0.05Mm (here, Mm refers to a mixed rare earth metal), Ti-0.5Ni-0.05Ru, and Ti-0.5Cu , Ti-1.0Cu, Ti-1.0Cu-0.5Nb, Ti-1.0Cu-1.0Sn-0.3Si-0.25Nb, Ti-0.5Al-0.45Si, Ti-0.9Al-0.35Si, Ti-3Al-2.5V , Ti-5Al-2.5Sn, Ti-6Al-2Sn-4Zr-2Mo, Ti-6Al-2.75Sn-4Zr-0.4Mo-0.45Si, etc.
作為α+β型鈦合金,例如有Ti-6Al-4V、Ti-6Al-6V-2Sn、Ti-6Al-7V、Ti-3Al-5V、Ti-5Al-2Sn-2Zr-4Mo-4Cr、Ti-6Al-2Sn-4Zr-6Mo、Ti-1Fe-0.35O、Ti-1.5Fe-0.5O、Ti-5Al-1Fe、Ti-5Al-1Fe-0.3Si、Ti-5Al-2Fe、Ti-5Al-2Fe-0.3Si、Ti-5Al-2Fe-3Mo、Ti-4.5Al-2Fe-2V-3Mo等。 Examples of the α + β-type titanium alloy include Ti-6Al-4V, Ti-6Al-6V-2Sn, Ti-6Al-7V, Ti-3Al-5V, Ti-5Al-2Sn-2Zr-4Mo-4Cr, and Ti- 6Al-2Sn-4Zr-6Mo, Ti-1Fe-0.35O, Ti-1.5Fe-0.5O, Ti-5Al-1Fe, Ti-5Al-1Fe-0.3Si, Ti-5Al-2Fe, Ti-5Al-2Fe- 0.3Si, Ti-5Al-2Fe-3Mo, Ti-4.5Al-2Fe-2V-3Mo, etc.
再者,作為β型鈦合金、例如有Ti-11.5Mo-6Zr-4.5Sn、Ti-8V-3Al-6Cr-4Mo-4Zr、Ti-10V-2Fe-3Mo、Ti-13V-11Cr-3Al、Ti-15V-3Al-3Cr-3Sn、Ti-6.8Mo-4.5Fe-1.5Al、Ti-20V-4Al-1Sn、Ti-22V-4Al等。 Examples of the β-type titanium alloy include Ti-11.5Mo-6Zr-4.5Sn, Ti-8V-3Al-6Cr-4Mo-4Zr, Ti-10V-2Fe-3Mo, Ti-13V-11Cr-3Al, and Ti -15V-3Al-3Cr-3Sn, Ti-6.8Mo-4.5Fe-1.5Al, Ti-20V-4Al-1Sn, Ti-22V-4Al, etc.
鈦複合材1,其表層部2、3之厚度若是過厚,則內層部4之厚度變薄,因此無法充分獲得機械特性提升效果。因此,表層部2、3之厚度,較佳的是相對鈦複合材1之全厚度每個單面為40%以下,更好的是每個單面25%以下。 If the thickness of the surface layer portions 2 and 3 of the titanium composite material 1 is too thick, the thickness of the inner layer portion 4 becomes thin, so that the effect of improving mechanical properties cannot be sufficiently obtained. Therefore, the thickness of the surface layer portions 2 and 3 is preferably 40% or less per one side, and more preferably 25% or less per one side relative to the full thickness of the titanium composite material 1.
另一方面,表層部2、3薄的情形下,內層部4之厚度變厚,因此機械特性提升效果增大。然而,表層部2、3若是過薄,則於將鈦複合材1加工時,表層部2、3破裂而內層部4出現於表面,以致位於內層部4之鈦化合物脫落、或是以出現於表面之鈦化合物為起點而發生表面破裂或端部破裂。又,水等之液體若是與其接觸,則會發生該液體侵入內層部4此一問題。因此,表層部2、3之厚度宜 設為0.1mm以上。 On the other hand, when the surface layer portions 2 and 3 are thin, the thickness of the inner layer portion 4 becomes thicker, so that the effect of improving mechanical properties is increased. However, if the surface layer portions 2 and 3 are too thin, when the titanium composite material 1 is processed, the surface layer portions 2 and 3 are broken and the inner layer portion 4 appears on the surface, so that the titanium compound located in the inner layer portion 4 falls off, or the Titanium compounds appearing on the surface are the starting point and surface cracks or end cracks occur. In addition, if a liquid such as water comes into contact with it, the problem that the liquid invades the inner layer portion 4 occurs. Therefore, the thickness of the surface layer portions 2 and 3 should preferably be 0.1 mm or more.
內層部4,係於鈦41中分散有鈦化合物42,具有於上述鈦化合物之周圍各自之構成元素(亦即,碳化物之周圍為碳、氮化物之周圍為氮、或是氧化物之周圍為氧)擴散之部分(圖示省略),且以面積率計具有大於0%且30%以下之空隙43。 The inner layer portion 4 is a titanium compound 42 dispersed in titanium 41 and has respective constituent elements around the titanium compound (that is, the periphery of the carbide is carbon, the periphery of the nitride is nitrogen, or an oxide). The surrounding area is oxygen) diffused (not shown), and has an area 43 in an area ratio of greater than 0% to 30%.
作為構成鈦複合材1之內層部4的鈦,例如可使用JIS1種~JIS4種之工業用純鈦。亦即,該鈦係作為一般之雜質含C:0.08%以下、H:0.013%以下、O:0.4%以下、N:0.05%以下、Fe:0.5%以下,且其餘部分為Ti之工業用純鈦。 As titanium constituting the inner layer portion 4 of the titanium composite material 1, industrial pure titanium of JIS1 to JIS4 can be used, for example. That is, the titanium system as a general impurity contains C: 0.08% or less, H: 0.013% or less, O: 0.4% or less, N: 0.05% or less, Fe: 0.5% or less, and the rest is Ti for industrial use. titanium.
特別是若是使用JIS1~3種之工業用純鈦,則將具有充分之加工性,而不會發生破裂等,且在熱加工後可獲得與形成上述表層部2、3之工業用純鈦一體化的鈦複合材1。 In particular, if JIS1 ~ 3 kinds of industrial pure titanium are used, they will have sufficient processability without cracking, etc., and they can be integrated with the industrial pure titanium forming the surface layer parts 2 and 3 after hot working. Of titanium composite material 1.
上述以外之其餘部分為雜質。作為雜質,可於不降低加工性及機械特性提升效果之範圍內含有。上述以外之雜質,主要而言,作為自邊角料混入之雜質元素,包括Al、V、Cr、Nb、Si、Sn、Mo及Cu等,與一般之雜質元素(C、N、Fe、O、H)合計,總量在5%以下可容許。 The rest other than the above are impurities. As an impurity, it can be contained in the range which does not reduce processability and the improvement effect of a mechanical characteristic. Impurities other than the above are mainly impurity elements mixed from scrap materials, including Al, V, Cr, Nb, Si, Sn, Mo, Cu, etc., and general impurity elements (C, N, Fe, O, H ) Total, the total is allowable below 5%.
內層部4,由於可使鈦複合材1具有良好之機械特性,其採用於鈦中分散有選自碳化物、氮化物及氧化物之1種以上的鈦化合物者。內層部4中,為了獲得上述之效果,碳,氮及氧之平均含量之合計宜為0.05~2.0質量%。各元素之平均含量之較佳範圍及限定理由敘述如下。 Since the inner layer portion 4 can provide the titanium composite material 1 with good mechanical properties, it is used in which one or more titanium compounds selected from carbides, nitrides, and oxides are dispersed in titanium. In order to obtain the above-mentioned effects in the inner layer portion 4, the total of the average contents of carbon, nitrogen, and oxygen is preferably 0.05 to 2.0% by mass. The preferable range of the average content of each element and the reason for limitation are described below.
C之平均濃度若是小於0.001%,則較表層部2、3更為提高內層部4之強度的效果幾乎無法確認,無法提升鈦複合材1之機械特性。另一方面,C之平均濃度若是大於0.1%,則會使內層部4之韌性劣化,以致熱加工或冷加工時破裂頻發、內層部4之板厚方向分斷、剝離,而有無法維持作為鈦複合材1之形狀的可能性。因此,內層部4之C的平均濃度宜設為0.001~0.1%。 If the average concentration of C is less than 0.001%, the effect of increasing the strength of the inner layer portion 4 more than the surface layer portions 2 and 3 can hardly be confirmed, and the mechanical properties of the titanium composite material 1 cannot be improved. On the other hand, if the average concentration of C is more than 0.1%, the toughness of the inner layer portion 4 will be deteriorated, resulting in frequent cracking during hot working or cold working, and the thickness and thickness of the inner layer portion 4 will be cut off and peeled off. Possibility to maintain the shape of the titanium composite material 1. Therefore, the average concentration of C in the inner layer portion 4 should be set to 0.001 to 0.1%.
N之平均濃度若是小於0.001%,則較表層部2、3更為提高內層部4之強度的效果幾乎無法確認,無法提升鈦複合材1之特性。另一方面,N之平均濃度若是大於0.5%,則會使內層部4之韌性劣化,以致熱加工或冷加工時破裂頻發、內層部4之板厚方向分斷、剝離,而有無法維持作為鈦複合材1之形狀的可能性。因此,內層部4之N的平均濃度宜設為0.001~0.5%。 If the average concentration of N is less than 0.001%, the effect of increasing the strength of the inner layer portion 4 more than the surface layer portions 2 and 3 can hardly be confirmed, and the characteristics of the titanium composite material 1 cannot be improved. On the other hand, if the average concentration of N is more than 0.5%, the toughness of the inner layer portion 4 will be deteriorated, resulting in frequent cracking during hot working or cold working, and the thickness and thickness of the inner layer portion 4 will be cut off and peeled off. Possibility to maintain the shape of the titanium composite material 1. Therefore, the average concentration of N in the inner layer portion 4 is preferably set to 0.001 to 0.5%.
O之平均濃度若是小於0.01%,則較表層部2、3更為提高內層部4之強度的效果幾乎無法確認,無法提升鈦複合材1之特性。另一方面,O之平均濃度若是大於1.0%,則會使內層部4之韌性劣化,以致熱加工或冷加工時破裂頻發、內層部4之板厚方向分斷、剝離,而有無法維持作為鈦複合材1之形狀的可能性。因此,內層部4之O的平均濃度宜設為0.01~1.0%。 If the average concentration of O is less than 0.01%, the effect of increasing the strength of the inner layer portion 4 more than the surface layer portions 2 and 3 can hardly be confirmed, and the characteristics of the titanium composite material 1 cannot be improved. On the other hand, if the average concentration of O is more than 1.0%, the toughness of the inner layer portion 4 will be deteriorated, resulting in frequent cracking during hot working or cold working, and the thickness and thickness of the inner layer portion 4 will be cut off and peeled off. Possibility to maintain the shape of the titanium composite material 1. Therefore, the average concentration of O in the inner layer portion 4 is preferably set to 0.01 to 1.0%.
表層部及內層部之成分分析,可由公知之方法(例如,JIS H 1612(1993)、JIS H 1614(1995)、JIS H 1615(1997)、JIS H 1617(1995)、JIS H 1619(2012)、JIS H 1620(1995))求得。又,此時,係自鈦複合材分別切出表層部及內層部後進行測定。表層部係以針對切削等加工所得之切粉等進行分析,內層部係以針對表層削除後之殘材採取分析試料後進行分析之情況效率為佳。分析試料係自表層部、內層部之板厚方向之中心部採取0.5g以上。若是表層部或內層部之厚度薄而無法獲得充分量之切粉的情形下,可進行鈦複合材之整體的成分分析,自其分析值、表層部或是內層部任一者之分析值、及各自之板厚,算出(逆算)表層或內層部之成分。 The composition analysis of the surface layer portion and the inner layer portion can be performed by a known method (for example, JIS H 1612 (1993), JIS H 1614 (1995), JIS H 1615 (1997), JIS H 1617 (1995), JIS H 1619 (2012 ), JIS H 1620 (1995)). At this time, the measurement was performed after cutting out the surface layer portion and the inner layer portion from the titanium composite material. The surface layer is used to analyze the cutting powder obtained by processing such as cutting, and the inner layer is used to analyze the residual material after the surface layer is removed. The analysis sample was taken from the central portion of the surface layer portion and the inner layer portion in the thickness direction of 0.5 g or more. If the thickness of the surface layer part or the inner layer part is thin and a sufficient amount of cut powder cannot be obtained, the entire component analysis of the titanium composite material can be performed, and the analysis value, surface layer part or inner layer part can be analyzed. Values and their respective plate thicknesses, and calculate (inversely calculate) the components of the surface layer or the inner layer portion.
鈦複合材1之空隙43之空隙率若是過多,則無法獲得作為塊狀金屬之機械特性(強度與延性)。另一方面,空隙 43雖期望愈少愈好,但為了將空隙完全壓著,則有於大的壓力下實施壓著之必要。其結果為,製造之鈦複合材1之形狀(厚度)受到限制,而且,製造成本也會增大。 If the porosity of the voids 43 of the titanium composite material 1 is too large, mechanical properties (strength and ductility) as a bulk metal cannot be obtained. On the other hand, although the number of voids 43 is preferably as small as possible, in order to completely press the voids, it is necessary to perform pressing under a large pressure. As a result, the shape (thickness) of the manufactured titanium composite material 1 is limited, and the manufacturing cost also increases.
另一方面,為了維持作為鈦複合材1之構造而以具有充分之機械特性(強度或延性等)之程度含有空隙43之情形下,內層部4之密度變低,而可謀求鈦複合材1之輕量化。 On the other hand, in order to maintain the structure as the titanium composite material 1 and contain the voids 43 to such an extent that it has sufficient mechanical characteristics (strength, ductility, etc.), the density of the inner layer portion 4 becomes low, and the titanium composite material can be obtained. Lightweight.
如以上所述,作為塊狀金屬之機械特性有所重要的情形下,係使空隙率降低,另一方面,以鈦複合材1之輕量化為優先的情形下,係使空隙率提高。如是,可配合用途選擇空隙率。此時之空隙率之範圍宜為大於0%且30%以下,更好的是大於0%且10%以下。又,藉由將空隙率設為10%以下,可具有較一般工業用純鈦不遜色之機械特性。 As described above, when the mechanical properties of the bulk metal are important, the porosity is reduced. On the other hand, when the weight reduction of the titanium composite 1 is given priority, the porosity is increased. If so, the porosity can be selected according to the application. The range of the porosity at this time is preferably greater than 0% and 30%, and more preferably greater than 0% and 10%. Moreover, by setting the porosity to 10% or less, it can have mechanical properties not inferior to those of general industrial pure titanium.
鈦複合材1之內層部4中殘存之空隙43的比率(空隙率),可如下算出。以鈦複合材1之與長度方向(輥軋方向)平行的厚度截面可觀察之方式埋入樹脂中後,使用金剛鑽或氧化鋁懸浮液將觀察面研磨(鏡面加工),予以最終加工成觀察用試料。 The ratio (void ratio) of the voids 43 remaining in the inner layer portion 4 of the titanium composite material 1 can be calculated as follows. After the titanium composite material 1 is embedded in the resin so that the thickness cross section parallel to the longitudinal direction (rolling direction) can be observed, the observation surface is ground (mirror-finished) using diamond diamond or alumina suspension, and finally processed for observation Sample.
接受該鏡面加工實施之觀察用試料,係以光學顯微鏡針對其不同位置之20個部位的厚度中心部拍攝。此處,中心部於鈦複合材1為板之情形下,係指板厚中心,為圓棒之情形下,係指圓截面之中心。測定由該光學顯微鏡照片觀察到之空隙43的面積比率,將20張照片之空 隙率的值平均之結果作為空隙率算出。 The observation sample subjected to the mirror surface processing was photographed with an optical microscope at the center of the thickness of 20 locations at different locations. Here, the center portion in the case where the titanium composite material 1 is a plate means the center of the plate thickness, and in the case where it is a round rod, it means the center of a circular cross section. The area ratio of the voids 43 observed in the optical microscope photograph was measured, and the average value of the void fraction values of the 20 photographs was calculated as the void fraction.
又,以光學顯微鏡拍攝組織照片時,係因應鈦複合材1之空隙之大小、或是空隙率而選擇適當之倍率。例如,空隙率為1%以下之情形下,因空隙少,故而宜以500倍程度之高倍率進行觀察,並作照片攝影。空隙率為10%以上之情形下,大的空隙變多,因此宜以20倍程度之低倍率進行觀察,並作照片攝影。又,空隙變小般之空隙率為1%以下之情形下,藉由使用可作偏光觀察之微分干涉顯微鏡,能夠較一般之光學顯微鏡更明晰地進行觀察。 Moreover, when taking a photograph of a tissue with an optical microscope, an appropriate magnification is selected in accordance with the size or void ratio of the titanium composite material 1. For example, when the void ratio is 1% or less, since there are few voids, it is advisable to observe at a high magnification of about 500 times and take a photograph. When the porosity is 10% or more, large voids increase, so it is appropriate to observe at a low magnification of about 20 times and take photos for photography. When the void ratio is 1% or less as the voids become smaller, a differential interference microscope capable of polarized observation can be used to observe more clearly than a general optical microscope.
如第1圖所示,鈦複合材1中之內層部4中,多量含有鈦化合物42。此一鈦化合物42,根據鈦複合材1之製造過程中的熱加工等,於鈦化合物42之周圍各自之構成元素(亦即,碳化物之周圍為碳、氮化物之周圍為氮、或氧化物之周圍為氧)會擴散至鈦41中,該無法固溶於鈦41之各構成元素,係以鈦化合物42以分散於鈦材41中之狀態殘存。此時,鈦化合物42係於加工(輥軋)方向排列,構成條狀化合物集合體42a。又,鈦化合物42,除完全形成化合物者以外,還包括內部存在有碳之化合物。例如,作為鈦化合物之素材使用碳之情形下,於熱軋等之製造過程中,碳雖與鈦反應形成鈦化合物,但有於該鈦化合物之內部殘存未與鈦反應完之碳的情形。 As shown in FIG. 1, a large amount of the titanium compound 42 is contained in the inner layer portion 4 in the titanium composite material 1. This titanium compound 42 is composed of respective constituent elements around the titanium compound 42 (that is, the periphery of the carbide is carbon, the periphery of the nitride is nitrogen, or oxidation) according to thermal processing or the like in the manufacturing process of the titanium composite material 1. The periphery of the object is oxygen) will diffuse into the titanium 41, and each of the constituent elements that cannot be dissolved in the titanium 41 remains in a state where the titanium compound 42 is dispersed in the titanium material 41. At this time, the titanium compounds 42 are aligned in the processing (rolling) direction to form a strip-shaped compound aggregate 42a. In addition, the titanium compound 42 includes a compound in which carbon is present in addition to a compound completely formed. For example, when carbon is used as a material of a titanium compound, although carbon reacts with titanium to form a titanium compound during the manufacturing process such as hot rolling, there may be cases where carbon that has not reacted with titanium remains in the titanium compound.
第2圖係示意性表示條狀化合物集合體42a的圖。如第2圖所示,條狀化合物集合體42a,意指鈦化合物42之粒子之中心間距離投影於輥軋方向的距離D(以下,稱為「粒子間距離」)為20μm以下的複數之鈦化合物42的集合體。又,本說明書中,粒子間距離超過20μm之情形下,將其視為其他之條狀化合物集合體。 Fig. 2 is a view schematically showing a strip-shaped compound aggregate 42a. As shown in FIG. 2, the strip-shaped compound aggregate 42 a means that the distance D between the centers of the particles of the titanium compound 42 projected in the rolling direction (hereinafter, referred to as “inter-particle distance”) is a plural number of 20 μm or less. An assembly of titanium compound 42. In addition, in this specification, when the distance between particles exceeds 20 micrometers, this is considered as another strip compound compound.
條狀化合物集合體42a,其厚度t(亦即,壓縮加工方向之大小)宜為100μm以下。這是因為,此一厚度若超過100μm,則於將鈦複合材加工時,以鈦化合物42為起點破裂發生之可能性增大所致。另一方面,有關條狀化合物集合體42a,其長度L(亦即,加工方向之大小)宜為厚度方向之大小(厚度)t的2.0倍以上(亦即,L/t≧2.0),更好的是3.0倍以上(亦即,L/t≧3.0)。這是因為,此一長度L若小,則受到抗拉應力時,以該鈦化合物為起點內層部易於破斷所致。又,宜設為L/t≦100,更好的是設為L/t≦40。 The thickness of the strip-shaped compound assembly 42a (that is, the size in the compression processing direction) is preferably 100 μm or less. This is because if the thickness exceeds 100 μm, the possibility of cracking from the titanium compound 42 as a starting point increases when the titanium composite material is processed. On the other hand, regarding the strip-shaped compound assembly 42a, the length L (that is, the size in the processing direction) should be 2.0 times or more the thickness (thickness) t in the thickness direction (that is, L / t ≧ 2.0), and more It is preferably 3.0 times or more (that is, L / t ≧ 3.0). This is because if the length L is small, the inner layer portion is easily broken when the titanium compound is used as a starting point when subjected to tensile stress. In addition, L / t ≦ 100 is preferable, and L / t ≦ 40 is more preferable.
條狀化合物集合體42a之大小(長度L及厚度t),係以下述方式算出。以鈦複合材1之與長度方向(輥軋方向)及厚度方向平行的截面(厚度截面)設為觀察面的方式埋入樹脂中後,使用金剛鑽或氧化鋁懸浮液研磨觀察面,予以最終加工成觀察用試料。 The size (length L and thickness t) of the strip-shaped compound aggregate 42a is calculated in the following manner. The titanium composite material 1 is embedded in the resin so that its cross-section (thickness cross-section) parallel to the length direction (rolling direction) and thickness direction is set as the observation surface, and the observation surface is polished with diamond or alumina suspension for final processing. Observation sample.
利用光學顯微鏡針對上述觀察面之厚度中心部的不同位置之20個部位作照片攝影。此處,厚度中心部 於鈦複合材1為板之情形下,係指板厚中心部,為圓棒之情形下,係指圓截面之中心。自所獲得之20張照片,測定條狀化合物集合體42a之長度L與厚度t,將各值之平均值作為長度L與厚度t,計算L/t。 Photographs were taken of 20 locations at different locations in the center of the thickness of the observation surface using an optical microscope. Here, the thickness center portion refers to the thickness center portion of the plate in the case where the titanium composite material 1 is a plate, and refers to the center of a circular section in the case of a round bar. From the obtained 20 photos, the length L and the thickness t of the strip-shaped compound aggregate 42a were measured, and the average value of each value was taken as the length L and the thickness t to calculate L / t.
鈦化合物42之各個粒子的周圍,存在有各構成元素(亦即,碳化物之情形下為碳、氮化物之情形下為氮、氧化物之情形下為氧)之擴散層。擴散層係指分散於內層部4之鈦41的鈦化合物42中,其構成元素(碳、氮或是氧)以鈦化合物42為中心向周邊之鈦41擴散,而形成有濃度梯度之層。 Around each particle of the titanium compound 42, there is a diffusion layer of each constituent element (that is, carbon in the case of carbide, nitrogen in the case of nitride, and oxygen in the case of nitride). The diffusion layer refers to a titanium compound 42 dispersed in the titanium 41 of the inner layer portion 4. The constituent element (carbon, nitrogen, or oxygen) diffuses to the surrounding titanium 41 with the titanium compound 42 as the center, and forms a layer having a concentration gradient. .
第3圖係表示於鈦複合材1之與長度方向(輥軋方向)及厚度方向平行的截面(厚度截面)中,1個粒子之厚度方向的距離與其周圍的構成元素濃度分布之概念的圖。擴散層係於製造鈦複合材1之過程中被加熱保持時(熱軋前之各加熱、熱軋中、熱軋後之熱處理等),自鈦化合物42之粒子,各構成元素擴散至周圍之鈦41所形成之層。如第3圖所示,擴散層中,各構成元素較內層部4之鈦41中所含之各構成元素的值為更多地含有。藉由此一擴散層存在,內層部4之鈦化合物42之粒子與鈦41強固地鍵結。因此,將鈦複合材1加工時,不會發生以鈦化合物42為起點之破裂。 FIG. 3 is a diagram showing the concept of the distance between the thickness direction of one particle and the concentration distribution of its constituent elements in a section (thickness section) of the titanium composite material 1 parallel to the length direction (rolling direction) and thickness direction. . The diffusion layer is diffused from the particles of the titanium compound 42 to the surroundings when the titanium composite 1 is heated and held (heating before hot rolling, heat treatment during hot rolling, heat treatment after hot rolling, etc.). A layer formed of titanium 41. As shown in FIG. 3, each of the constituent elements in the diffusion layer is contained more than the value of each constituent element contained in the titanium 41 of the inner layer portion 4. By this existence of a diffusion layer, the particles of the titanium compound 42 of the inner layer portion 4 and the titanium 41 are strongly bonded. Therefore, when the titanium composite material 1 is processed, cracking does not occur from the titanium compound 42 as a starting point.
此一擴散層可如以下般理解。以鈦複合材1之 與長度方向(輥軋方向)及厚度方向平行的截面(厚度截面)作為觀察面之方式埋入樹脂中之後,使用金剛鑽或氧化鋁懸浮液將觀察面研磨而予以最終加工成觀察用試料。使用EPMA,以上述觀察用試料中所觀察到之鈦化合物42的粒子為中心之方式於厚度方向進行線分析。分析之對象為各構成元素(亦即,碳化物之情形為碳、氮化物之情形為氮、氧化物之情形為氧)。以內層部4之鈦41之值為基準,濃度較其為高且不含粒子之區域乃為擴散層。 This diffusion layer can be understood as follows. After the titanium composite material 1 is embedded in the resin with a section (thickness section) parallel to the longitudinal direction (rolling direction) and the thickness direction as the observation surface, the observation surface is ground using diamond diamond or alumina suspension for final processing Observation sample. Using EPMA, line analysis was performed in the thickness direction with the particles of the titanium compound 42 observed in the observation sample as the center. The analysis target is each constituent element (that is, the case of carbide is carbon, the case of nitride is nitrogen, and the case of oxygen is oxygen). Based on the value of titanium 41 in the inner layer portion 4, a region having a higher concentration and containing no particles is a diffusion layer.
上述之擴散層之厚度,會因各種因子而變化。例如,添加鈦化合物之情形下,其係由(1)鈦化合物之分解、(2)朝向周邊之各構成元素之擴散而形成,因此該厚度係因鈦化合物之分解速度與各構成元素在鈦材內之擴散速度而變化。又,還會因製造時之熱履歷而變化。再者,還會因作為熱軋素材之捆包體加熱時之與海綿鈦等之鈦化合物的接觸程度而變化。故而,擴散層之厚度即使在同一複合材中也具有各種擴散層之厚度,難以一概決定,但其係以鈦化合物與各構成元素將存在或已存在之部分為中心多量地形成。 The thickness of the above-mentioned diffusion layer may vary due to various factors. For example, when a titanium compound is added, it is formed by (1) decomposition of the titanium compound and (2) diffusion of each constituent element toward the periphery. Therefore, the thickness is due to the decomposition rate of the titanium compound and the constituent elements in titanium. The diffusion speed in the material varies. In addition, it may change due to the thermal history at the time of manufacture. Furthermore, the degree of contact with a titanium compound such as sponge titanium when the package body as a hot-rolled material is heated may vary. Therefore, the thickness of the diffusion layer has various thicknesses of the diffusion layer even in the same composite material, which is difficult to determine uniformly, but it is formed in a large amount around the titanium compound and each constituent element to be present or existing.
相對鈦複合材1之全厚度的內層部4之厚度愈厚,則機械特性愈為提升,因此較佳的是相對鈦複合材1之全厚度大於20%,更好的是大於50%。另一方面,愈厚則加工性愈是劣化,因此內層部4之厚度較佳的是相對鈦複合材1之 全厚度設為95%以下。 The thicker the thickness of the inner layer portion 4 relative to the full thickness of the titanium composite 1 is, the more the mechanical properties are improved. Therefore, it is preferable that the total thickness of the titanium composite 1 is greater than 20%, and more preferably greater than 50%. On the other hand, as the thickness becomes thicker, the workability deteriorates. Therefore, the thickness of the inner layer portion 4 is preferably set to 95% or less with respect to the total thickness of the titanium composite material 1.
鈦捆包體5具備鈦捆包材6與填充材7、8。鈦捆包體5之形狀不限於特定之形狀,而是由製造之鈦複合材1之形狀所決定。製造板材之鈦複合材1時,使用長方體形狀之鈦捆包體5。又,製造圓棒、線材、甚或擠壓材之鈦複合材1的情形下,乃使用圓柱形或八角柱等多角柱形狀之鈦捆包體5。鈦捆包體5之大小係由製品之大小(厚度、寬度及長度)及製造量(質量)所決定。 The titanium packing body 5 includes a titanium packing material 6 and fillers 7 and 8. The shape of the titanium bundle body 5 is not limited to a specific shape, but is determined by the shape of the titanium composite material 1 to be manufactured. When manufacturing the titanium composite material 1 of a plate material, the titanium bundle body 5 of a rectangular parallelepiped shape is used. Moreover, in the case of manufacturing the titanium composite material 1 of a round rod, a wire, or even an extruded material, a titanium packing body 5 having a polygonal column shape such as a cylindrical shape or an octagonal column is used. The size of the titanium package 5 is determined by the size (thickness, width, and length) of the product and the manufacturing quantity (quality).
鈦捆包材6與鈦複合材1之表層部2、3相同,使用屬於JIS1種~JIS4種之工業用純鈦或鈦合金材。 The titanium packing material 6 is the same as the surface layer portions 2 and 3 of the titanium composite material 1, and industrial pure titanium or titanium alloy materials belonging to JIS1 to JIS4 are used.
鈦捆包材6之形狀,係依存於作為熱加工用素材使用之鈦捆包體5的形狀,因此並無特別定形,可使用板材與管材等。 The shape of the titanium packaging material 6 depends on the shape of the titanium packaging body 5 used as a material for thermal processing. Therefore, there is no particular shape, and a plate material, a pipe material, or the like can be used.
為了使經由熱加工及冷加工、退火等製造步驟所製造之鈦複合材1具有優異之表面性狀、內層部4之保持狀態、及加工性,鈦捆包材6之厚度乃為重要。 In order for the titanium composite material 1 produced through manufacturing steps such as hot working, cold working, and annealing to have excellent surface properties, a retained state of the inner layer portion 4, and workability, the thickness of the titanium packaging material 6 is important.
鈦捆包材6之厚度小於1mm而為薄的情形下, 伴隨著塑性變形而於熱加工之途中,鈦捆包材6會破斷,以致鈦捆包體5內部之一部分脫落。此一情形下,同時真空破壞,以致鈦捆包體5之內部所填充之鈦材7產生氧化。又,鈦捆包體5之內部所填充之鈦材7的起伏會轉印到鈦捆包體5之表面,以致還有熱加工中產生大的表面起伏之虞。 When the thickness of the titanium packaging material 6 is thinner than 1 mm, the titanium packaging material 6 may be broken during thermal processing along with plastic deformation, so that a part of the inside of the titanium packaging body 5 may fall off. In this case, the vacuum breaks at the same time, so that the titanium material 7 filled in the titanium packing body 5 is oxidized. In addition, the undulations of the titanium material 7 filled in the titanium packing body 5 are transferred to the surface of the titanium packing body 5 so that there is a possibility that large surface undulations are generated during thermal processing.
此等情事的結果為,製造之鈦複合材1,表面性狀或延性等之機械特性劣化。再者,鈦捆包材6若是變得過薄,則有無法支持內部填充之鈦材7的重量之虞。因此,在室溫與熱間保持或是加工中,鈦捆包體5之剛性會不足而有變形之虞。 As a result of these events, mechanical properties such as surface properties and ductility of the manufactured titanium composite material 1 are deteriorated. Furthermore, if the titanium packing material 6 becomes too thin, there is a possibility that the weight of the titanium material 7 which is filled internally cannot be supported. Therefore, the rigidity of the titanium bundle 5 may be insufficient during the maintenance or processing between room temperature and heat, and there is a risk of deformation.
為了可在不發生此等問題下進行熱加工,而製造具有優異之表面性狀、內層部4之保持狀態及加工性的鈦複合材1,鈦捆包材6之厚度宜為1mm以上,更好的是2mm以上。 In order to manufacture the titanium composite material 1 having excellent surface properties, the holding state and workability of the inner layer portion 4 without performing such problems, the thickness of the titanium packing material 6 should be 1 mm or more, more It is more than 2mm.
再者,鈦捆包材6之厚度,宜為鈦捆包體5之全厚度之25%以下。鈦捆包材6之厚度若較鈦捆包體5之全厚度之25%為厚,則製造上雖無特別問題,但鈦捆包體5之全厚度中所占之鈦捆包材6之比率增大,且內部或內層部4之厚度變薄。因此,鈦捆包體5內部之鈦化合物量變少,機械特性提升效果趨低,因此不令人滿意。 Moreover, the thickness of the titanium packing material 6 is preferably 25% or less of the full thickness of the titanium packing body 5. If the thickness of the titanium packaging material 6 is thicker than 25% of the total thickness of the titanium packaging body 5, although there is no particular problem in manufacturing, the titanium packaging material 6 occupies the entire thickness of the titanium packaging body 5. The ratio increases, and the thickness of the inner or inner layer portion 4 becomes thin. Therefore, the amount of the titanium compound in the titanium packing body 5 is reduced, and the effect of improving the mechanical properties is lowered, which is not satisfactory.
作為填充材之鈦材7,係選自海綿鈦、鈦塊體及鈦邊角料之1種以上。 The titanium material 7 as a filler is one or more selected from the group consisting of sponge titanium, titanium blocks, and titanium scraps.
鈦材7之化學組成,可使用相當於JIS1種~JIS4種之工業用純鈦。亦即,具有C:0.08%以下、H:0.013%以下、O:0.4%以下、N:0.05%以下、Fe:0.5%以下、其餘部分Ti及雜質之化學組成。 For the chemical composition of the titanium material 7, industrial pure titanium equivalent to JIS1 to JIS4 can be used. That is, it has the chemical composition of C: 0.08% or less, H: 0.013% or less, O: 0.4% or less, N: 0.05% or less, Fe: 0.5% or less, and the rest of Ti and impurities.
作為鈦材7,可使用先前之克羅爾法等之製鍊步驟所製造的一般之海綿鈦。其大小宜為平均粒徑20mm以下。平均粒徑若較20mm為大,則與鈦化合物等之粉末8均一地混合困難,以致熱加工所製造之鈦複合材1之內層部4內有發生鈦化合物不均一之虞。另一方面,平均粒徑小的情況下,在特性層面雖無問題,但鈦材7之平均粒徑若是小於0.5mm,則破碎需要時間,而且微細粉塵之發生也多且會飛散,因此製造效率趨劣。因此,鈦材之平均粒徑較佳的是0.5mm以上。 As the titanium material 7, a general sponge titanium produced by a chain-forming process such as the Kroll method can be used. Its size should be less than 20mm. If the average particle diameter is larger than 20 mm, it is difficult to uniformly mix the powder 8 with a titanium compound or the like, so that the titanium compound 1 in the inner layer portion 4 of the titanium composite material produced by thermal processing may be uneven. On the other hand, if the average particle diameter is small, there is no problem in terms of characteristics. However, if the average particle diameter of the titanium material 7 is less than 0.5 mm, it will take time to break, and fine dust will be generated and scattered. Inferior efficiency. Therefore, the average particle diameter of the titanium material is preferably 0.5 mm or more.
作為鈦材7,可使用鈦邊角料。例如,鈦邊角料包括工業用純鈦材之製造步驟中所發生之無法成為製品的下腳料、為了將工業用純鈦素材形成為製品形狀而於切削、研削時所發生之鈦切粉、及作為製品使用後之變得不必要之工業用純鈦材等。鈦邊角料若是過大,則有搬送困 難及難以置入鈦捆包體5此等問題,因此期望能適度切斷。 As the titanium material 7, a titanium scrap can be used. For example, titanium scraps include scraps that cannot be made into products during the manufacturing steps of industrial pure titanium materials, titanium cutting powders that occur during cutting and grinding in order to form industrial pure titanium materials into product shapes, and as Pure titanium material for industrial use which becomes unnecessary after the product is used. If the titanium scrap is too large, there are problems such as difficulty in transportation and difficulty in placing the titanium packing body 5, and therefore, moderate cutting is desired.
海綿鈦或是鈦邊角料為塊狀,因此在素材之間會有空隙(間隙)9。為了提升海綿鈦等之處理性,或是減少此等空隙,可預先將海綿鈦等及鈦化合物等之粉末8混合後予以壓縮成形,而形成為第5圖所示般之塊體10後,再置入鈦捆包體5。 Sponge titanium or titanium scraps are block-shaped, so there will be gaps (gap) 9 between the materials. In order to improve the rationality of sponge titanium, etc., or reduce these voids, powders 8 of sponge titanium and titanium compounds and the like can be mixed and compressed in advance to form a block 10 as shown in FIG. 5. Then, a titanium bundle body 5 was placed.
鈦化合物等之粉末8,例如在碳化物之情形下,可例示碳粉末、TiC粉末等,在氮化物之情形下,除TiN粉末之外,可例示Fe3N粉末、Fe4N粉末等(惟內層部4之鈦之Fe濃度不得超過JIS規格),在氧化物之情形下,除TiO粉末、TiO2粉末、Ti2O3粉末以外,可例示FeO粉末、Fe2O3粉末與Fe3O4粉末等(惟內層部4之鈦之Fe濃度不得超過JIS規格)。此等粉末8可使用市售者。 Examples of powders 8 of titanium compounds include carbon powders and TiC powders in the case of carbides, and Fe 3 N powders and Fe 4 N powders in the case of nitrides in addition to TiN powders. (However, the Fe concentration of titanium in the inner layer portion 4 must not exceed the JIS standard.) In the case of oxides, in addition to TiO powder, TiO 2 powder, and Ti 2 O 3 powder, FeO powder, Fe 2 O 3 powder, and Fe 3 O 4 powder, etc. (except that the Fe concentration of titanium in the inner layer portion 4 must not exceed the JIS standard). These powders 8 can be used commercially.
鈦化合物等之粉末8之平均粒徑若是大於50μm,則與鈦材7均一混合困難。因此,於鈦複合材1之內層部4內將無法將鈦化合物均一分散。因此,鈦化合物等之粉末8之平均粒徑宜為50μm以下。 If the average particle diameter of the powder 8 of the titanium compound or the like is larger than 50 μm, it will be difficult to uniformly mix the powder with the titanium material 7. Therefore, the titanium compound cannot be uniformly dispersed in the inner layer portion 4 of the titanium composite material 1. Therefore, the average particle diameter of the powder 8 of the titanium compound or the like is preferably 50 μm or less.
另一方面,鈦化合物等之粉末8之平均粒徑較 小的情形下,在特性層面雖無問題,但若是過小,則與鈦材7混合時、或是填充於鈦捆包體5中時,粉塵之飛散將會成為問題,而有為作業帶來障礙之虞。因此,鈦化合物等之粉末8之平均粒徑較佳的是0.1μm以上。 On the other hand, when the average particle diameter of the powder 8 such as a titanium compound is small, there is no problem in terms of characteristics, but if it is too small, it is mixed with the titanium material 7 or filled with the titanium bundle 5 , The scattering of dust will become a problem, and it may cause obstacles to operation. Therefore, the average particle diameter of the powder 8 of the titanium compound or the like is preferably 0.1 μm or more.
鈦捆包體5內之空隙43內若是有空氣殘存,則熱加工前之加熱時,鈦材7會氧化暨氮化,以致製造之鈦複合材1之延性降低。因此,有效的是將鈦捆包體5內減壓形成為高真空。 If air remains in the voids 43 in the titanium bundle body 5, the titanium material 7 will be oxidized and nitrided when heated before hot working, so that the ductility of the manufactured titanium composite material 1 is reduced. Therefore, it is effective to reduce the pressure inside the titanium package 5 to a high vacuum.
為了防止熱加工時之鈦材7之氧化暨氮化,將鈦捆包體5之內部壓力(絕對壓)設為10Pa以下,較佳的是設為1Pa以下即可。鈦捆包體5之內部壓力若較10Pa為大,則因殘留之空氣鈦材7會氧化或氮化。將內部壓力設為極端之小此舉,則須提升裝置之氣密性、及增強真空排氣裝置等,而與製造成本之增大息息相關,因此內部壓力之下限宜設為1×10-3Pa。 In order to prevent oxidation and nitridation of the titanium material 7 during hot working, the internal pressure (absolute pressure) of the titanium bundle body 5 is set to 10 Pa or less, preferably 1 Pa or less. If the internal pressure of the titanium package 5 is greater than 10 Pa, the titanium material 7 will be oxidized or nitrided due to the remaining air. If the internal pressure is set to be extremely small, it is necessary to improve the airtightness of the device and enhance the vacuum exhaust device, which are closely related to the increase in manufacturing costs. Therefore, the lower limit of the internal pressure should be set to 1 × 10 -3 Pa.
鈦複合材1係藉由對鈦捆包體5進行熱加工或進一步冷加工而製造。 The titanium composite material 1 is produced by hot working or further cold working the titanium package 5.
熱加工之方法可根據製品之形狀而選擇。於製造板材 之鈦複合材1的情形下,係將長方體形狀(扁胚)之鈦捆包體5加熱並進行熱軋,而形成為鈦板。因應必要,與先前步驟相同,可於熱軋後將表面之氧化層以酸洗等除去後,再進行冷軋,並進一步予以薄化加工。 The method of thermal processing can be selected according to the shape of the product. In the case of manufacturing a titanium composite material 1 of a plate material, a titanium package 5 having a rectangular parallelepiped shape (flat embryo) is heated and hot-rolled to form a titanium plate. If necessary, as in the previous step, the surface oxide layer can be removed by pickling or the like after hot rolling, and then cold rolled and further thinned.
於製造圓棒或線材之鈦複合材1的情形下,係將圓柱或多角形形狀(小胚)之鈦捆包體5加熱,並進行熱軋或熱擠壓,而形成為鈦圓棒或線材。又,因應必要,與先前步驟相同,可於熱加工後將氧化層以酸洗等除去後,再進行冷軋,並進一步予以細化加工。 In the case of manufacturing the titanium composite material 1 of round rods or wires, the cylindrical or polygonal (small embryo) titanium bundle 5 is heated and hot-rolled or hot-extruded to form a titanium round rod or Wire. In addition, if necessary, as in the previous step, the oxide layer can be removed by pickling or the like after hot working, and then cold rolled, and further refined.
進而,於製造擠壓型材之鈦複合材1之情形下,係將圓柱或多角形形狀(小胚)之鈦捆包體5加熱,並進行熱擠壓,而形成為各種截面形狀之鈦型材。作為熱加工前之加熱溫度,採用與一般之鈦扁胚或小胚熱加工之情況相同之加熱溫度即可。加熱溫度雖依鈦捆包體5之大小與熱加工之程度(加工率)而異,但宜加熱於600℃以上且1200℃以下。 Further, in the case of manufacturing the titanium composite material 1 of extruded profiles, the titanium bundle body 5 having a cylindrical or polygonal shape (small embryo) is heated and hot-extruded to form titanium profiles of various cross-sectional shapes. . As the heating temperature before hot working, the same heating temperature as in the case of general hot processing of titanium flat embryos or small embryos may be adopted. Although the heating temperature varies depending on the size of the titanium bundle body 5 and the degree of heat processing (processing ratio), it is preferable to heat the temperature to 600 ° C or higher and 1200 ° C or lower.
加熱溫度若是過低,則鈦捆包體5之高溫強度變高,變形能低,因此熱加工中易於發生破裂。特別是鈦捆包體5之熔接部破裂而內部露出以致一部分脫落、或是內部氧化,若是如此,鈦複合材1將難以獲得必要之特性。又,鈦化合物之粒子之周圍的構成元素之擴散層也不會形成,內層部之鈦化合物之粒子與鈦無法充分鍵結。因 此,鈦複合材加工時會有以鈦化合物為起點而發生破裂之情形。另一方面,加熱溫度若是過高,則所獲得之鈦複合材1之組織粗化,而無法獲得充分之材料特性。此外,因氧化之故表面之捆包材6會減薄。因此,加熱溫度推薦的是設為600℃~1200℃。 If the heating temperature is too low, the high-temperature strength of the titanium bale body 5 becomes high, and the deformation energy is low. Therefore, cracking easily occurs during hot working. In particular, the welded portion of the titanium package 5 is broken and exposed to the inside so that part of it is detached or internally oxidized. If this is the case, it is difficult for the titanium composite material 1 to obtain necessary characteristics. Further, the diffusion layer of the constituent elements around the particles of the titanium compound is not formed, and the particles of the titanium compound in the inner layer portion and the titanium cannot be sufficiently bonded. Therefore, when the titanium composite material is processed, cracks may occur starting from the titanium compound. On the other hand, if the heating temperature is too high, the structure of the obtained titanium composite material 1 is coarsened, and sufficient material characteristics cannot be obtained. In addition, the packaging material 6 on the surface is thinned due to oxidation. Therefore, the recommended heating temperature is 600 ° C to 1200 ° C.
熱加工時之加工程度,亦即加工率,可為了控制鈦複合材1之內層部4之空隙率而選擇。此處所稱之加工率,係將鈦捆包體5之截面積與熱加工後之鈦複合材1之截面積的差,除以鈦捆包體5之截面積所得之比率(百分率)。 The degree of processing during hot working, that is, the processing rate, can be selected in order to control the porosity of the inner layer portion 4 of the titanium composite material 1. The processing rate referred to herein is a ratio (percentage) obtained by dividing the difference between the cross-sectional area of the titanium bale body 5 and the cross-sectional area of the titanium composite material 1 after hot working by the cross-sectional area of the titanium bale body 5.
此一加工率低的情形下,鈦捆包體5內部之空隙43未能充分壓著,因此即使是熱加工後,仍以空隙43之原狀殘存。此類空隙多量含有之鈦複合材1,相應於含有之空隙之程度將會成為輕量,對機械特性提升效果不會構成問題。惟因內層部4中存在之空隙43多,而無法充分獲得機械特性。另一方面,加工率若是增大,則空隙率降低而機械特性提升。因此,製造之鈦複合材1之機械特性受到重視的情形下,加工率宜為高。 In the case where the processing rate is low, the voids 43 inside the titanium packing body 5 are not sufficiently pressed. Therefore, even after the hot working, the voids 43 remain as they are. Such a titanium composite material 1 containing a large amount of voids will be lightweight to a degree corresponding to the voids contained therein, and it will not pose a problem in improving the mechanical properties. However, because there are many voids 43 in the inner layer portion 4, the mechanical characteristics cannot be sufficiently obtained. On the other hand, if the processing rate is increased, the porosity is reduced and the mechanical characteristics are improved. Therefore, when the mechanical characteristics of the manufactured titanium composite material 1 are valued, the processing rate should be high.
熱軋後,可供於退火、冷軋。鈦複合材1,不論是熱加工材(例如熱軋板)或是冷加工材(例如冷軋板),機械特性提升效果並無大差別。又,表面狀態也是不論輥軋後之 原狀、酸洗加工後、退火加工後之任一種狀態下均屬良好,機械特性提升效果不變。 After hot rolling, it can be used for annealing and cold rolling. Whether the titanium composite material 1 is a hot-worked material (for example, a hot-rolled sheet) or a cold-worked material (for example, a cold-rolled sheet), the effect of improving mechanical properties is not much different. In addition, the surface state is good regardless of the original state after rolling, after pickling, and after annealing, and the effect of improving mechanical properties remains unchanged.
鈦材7中有必要將鈦化合物等之粉末8均一且高密度地填充。為此,可將此等鈦材7及鈦化合物等之粉末8填充於容器使其旋轉或振動,而將內部之鈦材7及鈦化合物等之粉末8以均一分散之方式混合即可。 In the titanium material 7, it is necessary to fill the powder 8 of a titanium compound or the like uniformly and at a high density. To this end, the titanium material 7 and the powder 8 of the titanium compound may be filled in a container to be rotated or vibrated, and the internal titanium material 7 and the powder 8 of the titanium compound may be uniformly dispersed.
攪拌之方法,可例舉的有:將容器於上下方向旋轉、自水平傾斜20~70°斜向旋轉、將容器作上下方向或水平方向等之振動、或是於容器內插入攪拌件令攪拌件旋轉之方法等等。 The stirring method can be exemplified by rotating the container in an up-down direction, obliquely rotating from a horizontal tilt of 20 to 70 °, vibrating the container in an up-down or horizontal direction, or inserting a stirring member into the container to stir How to rotate the pieces and so on.
攪拌時間係依容器之大小或混合之鈦材7、及鈦化合物等之粉末8的量而變化,宜為1~30分鐘。若是考慮生產性,較佳的是以數分鐘間可均一混合之方式,決定容器之大小或處理量。 The stirring time varies depending on the size of the container or the amount of the titanium material 7 and the powder 8 of the titanium compound to be mixed, and is preferably 1 to 30 minutes. If productivity is taken into consideration, it is preferable to determine the size or processing capacity of the container in such a way that it can be uniformly mixed within a few minutes.
混合之鈦材7與鈦化合物等之粉末8,係原狀填充入鈦捆包體5內。或是,為了提升鈦材7之處理性或減少上述此等空隙,可予壓縮成形為如第5圖所示般之鈦塊體10後,再納入鈦捆包體5內。 The mixed titanium material 7 and powder 8 of a titanium compound and the like are filled in the titanium packing body 5 as they are. Alternatively, in order to improve the rationality of the titanium material 7 or reduce the above-mentioned voids, it may be compression-molded into a titanium block 10 as shown in FIG. 5 and then incorporated into the titanium bundle body 5.
將鈦捆包材6利用熔接部11熔接之方法,可例示的有 TIG熔接或是MIG熔接等之電弧熔接、以及電子束熔接或雷射熔接等,並無特別限定。其中,熔接氛圍,為使鈦材7及鈦捆包材6之面不致氧化或氮化,宜於真空氛圍或惰性氣體氛圍下進行熔接。 Examples of the method for welding the titanium packaging material 6 by the welding portion 11 include arc welding such as TIG welding or MIG welding, and electron beam welding or laser welding, which are not particularly limited. Among them, the welding atmosphere is suitable for welding in a vacuum atmosphere or an inert gas atmosphere so that the surfaces of the titanium material 7 and the titanium packing material 6 are not oxidized or nitrided.
於將鈦捆包材6之接縫(熔接部11)最後熔接時,較佳的是將鈦捆包體5置入真空氛圍之容器(腔室)內進行熔接,使鈦捆包體5之內部保持真空。 When the seam (welding portion 11) of the titanium packing material 6 is finally welded, it is preferable to place the titanium packing body 5 in a container (chamber) in a vacuum atmosphere for welding, so that the titanium packing body 5 Vacuum is maintained inside.
如第6圖所示,可將與鈦化合物等之粉末8混合並壓縮成形之鈦塊體10以作為捆包材之鈦韌材(伸展材)被覆,並將鈦韌材之全周圍作接縫熔接(使用旋轉電極之電阻熔接)予以密閉,而製造鈦捆包體12。此時,可經由事前於端部開孔而於該處硬焊熔接之銅管,將鈦韌材之內部減壓至特定之壓力,並於減壓後將銅管壓著,而維持鈦韌材內部之壓力。 As shown in FIG. 6, a titanium block 10 which is mixed with powder 8 of a titanium compound and the like and is compression-molded may be coated with a titanium tough material (stretch material) as a packing material, and the entire periphery of the titanium tough material may be connected. The seam welding (resistance welding using a rotating electrode) was sealed, and the titanium bundle body 12 was manufactured. At this time, the titanium tube can be depressurized to a specific pressure through a copper tube that has been previously holed at the end and brazed and welded there, and the copper tube can be pressed after decompression to maintain the titanium toughness. Pressure inside the material.
除了具有高抗拉強度與良好之加工性以外,可以低成本製造,因此可作為汽車等之陸上輸送機器之結構構件使用。 In addition to having high tensile strength and good processability, it can be manufactured at low cost, so it can be used as a structural member of land transportation equipment such as automobiles.
製造表1所示之鈦捆包體,對於此鈦捆包體以表1所示之製作步驟製造鈦複合材1(板材)。 The titanium bundles shown in Table 1 were manufactured, and titanium composite materials 1 (plate materials) were manufactured by the manufacturing steps shown in Table 1 for the titanium bundles.
作為填充材,使用以克羅爾法製造之粒度2.5 mm以上且6mm以下,化學組成相當於JIS1種(C:0.002%、H:0.001%、O:0.03%、N:0.001%、Fe:0.03%、其餘部分Ti及雜質)之海綿鈦。又,作為填充材,使用市售之TiO2粉末(平均粒徑2μm)、TiC粉末(平均粒徑3μm)或TiN粉末(平均粒徑5μm)。 As the filler, a particle size of 2.5 mm to 6 mm manufactured by the Kroll method is used, and the chemical composition is equivalent to JIS1 (C: 0.002%, H: 0.001%, O: 0.03%, N: 0.001%, Fe: 0.03). %, The rest of Ti and impurities) of sponge titanium. As the filler, commercially available TiO 2 powder (average particle diameter of 2 μm), TiC powder (average particle diameter of 3 μm), or TiN powder (average particle diameter of 5 μm) was used.
將上述之海綿鈦與鈦化合物等之粉末以特定量投入V型混合器混合。將混合後之素材投入模具壓縮成形,形成厚度15mm、寬度50mm、長度60mm之第5圖所示的鈦塊體。作為比較,試料No.11中,係於僅添加海綿鈦粒子7而不添加粉末原料8下作成鈦塊體。 The above-mentioned powders of sponge titanium and titanium compounds are put into a V-type mixer in a specific amount and mixed. The mixed material was put into a mold for compression molding to form a titanium block shown in Fig. 5 with a thickness of 15 mm, a width of 50 mm, and a length of 60 mm. For comparison, in Sample No. 11, a titanium block was prepared by adding only sponge titanium particles 7 without powder raw materials 8.
作為鈦捆包材,係採用包含JIS1種(TP270C;C:0.001%、H:0.005%、O:0.04%、N:0.001%、Fe:0.03%、其餘部分Ti及雜質)或JIS2種(TP340C;C:0.002%、H:0.004%、O:0.09%、N:0.001%、Fe:0.05%、其餘部分Ti及雜質)工業用純鈦材且厚度為1.0mm之薄板。 As the titanium packing material, one type of JIS (TP270C; C: 0.001%, H: 0.005%, O: 0.04%, N: 0.001%, Fe: 0.03%, the rest of Ti and impurities) or JIS (TP340C) is used. ; C: 0.002%, H: 0.004%, O: 0.09%, N: 0.001%, Fe: 0.05%, the rest of Ti and impurities) industrial pure titanium material and a thickness of 1.0mm.
如第6圖所示,將鈦塊體以作為捆包材之工業用純鈦材被覆,將工業用純鈦材之全周圍以接縫熔接(使用旋轉電極之電阻熔接)予以密閉。對於此一工業用純鈦材,事前於端部開孔而於該處硬焊熔接銅管。接縫熔接後,經由銅管將工業用純鈦材之內部減壓至特定之壓力(0.06~1.2Pa),減壓後將銅管壓著而保持工業用純鈦材內部之壓力。試料No.12中,係於減壓至38Pa時,壓著銅管而形成為捆包體。 As shown in FIG. 6, the titanium block is coated with industrial pure titanium material as a packing material, and the entire periphery of the industrial pure titanium material is sealed by seam welding (resistance welding using rotating electrodes) and sealed. For this industrial pure titanium material, a hole was opened in advance at the end and the copper pipe was brazed and welded there. After the joints are welded, the inside of the industrial pure titanium material is decompressed to a specific pressure (0.06 ~ 1.2Pa) through the copper tube. After the pressure is reduced, the copper tube is pressed to maintain the internal pressure of the industrial pure titanium material. In Sample No. 12, when the pressure was reduced to 38 Pa, the copper tube was pressed to form a packing body.
製作之鈦捆包體,係於大氣氛圍下,以850℃作4小時加熱後,進行熱軋,製作厚度2.0mm之鈦複合材。對此鈦複合材,係於725℃下作15分鐘退火後,予以酸洗而除去表層之積垢,供於組織觀察及拉伸試驗。 The produced titanium package was heated at 850 ° C for 4 hours in an atmospheric atmosphere, and then hot-rolled to produce a titanium composite material having a thickness of 2.0 mm. This titanium composite was annealed at 725 ° C for 15 minutes, and then acid-washed to remove the scale on the surface layer, which was used for tissue observation and tensile test.
為了使鈦複合材之與長度方向(輥軋方向)及厚度方向平行的截面(厚度截面)可觀察而予埋入樹脂後,使用金剛鑽或是氧化鋁懸浮液研磨觀察面(鏡面加工),而予以最終加工成觀察用試料。空隙率係利用光學顯微鏡,將上述觀察用試料之厚度中心部作20個部位之照片攝影,就各張照片測定空隙之面積率求取其等之平均值。條狀化合物集合體,係利用光學顯微鏡觀察上述觀察用試料之厚度中心部,求得其形態。又,針對觀察之條狀化合物集合體20個,測定其厚度t與長度L並算出L/t,求取其等之平均值。 In order to observe the cross section (thickness cross section) parallel to the length direction (rolling direction) and thickness direction of the titanium composite material, after the resin is embedded, the observation surface is polished with diamond or alumina suspension (mirror surface processing), and It was finally processed into observation samples. The porosity was measured by taking 20 photos of the central part of the thickness of the observation sample with an optical microscope, and the area ratio of the voids was measured for each photo to obtain the average value. The strip-shaped compound aggregate was obtained by observing the thickness center portion of the observation sample with an optical microscope to determine its morphology. In addition, about 20 strip-shaped compound aggregates to be observed, the thickness t and the length L were measured, L / t was calculated, and the average value of these was calculated.
擴散層之厚度,針對添加TiO2粉末、TiC粉末、TiN粉末之No.2、No.4、No.6,就上述觀察用試料之厚度中心部觀察到之條狀化合物集合體5個,將其中觀察到之3個鈦化合物之粒子以EPMA測定。以鈦化合物之粒子成為中心之方式於厚度方向進行線分析,將內層部之鈦之值作為基準,測定較其鈦化合物之構成元素(碳、氮或氧)濃度高、不含粒子之單側區域之距離,將其等平均之,作為條狀化合物集合體各者之擴散層的厚度求得。 For the thickness of the diffusion layer, with respect to No. 2, No. 4, and No. 6 in which TiO 2 powder, TiC powder, and TiN powder were added, five strip-shaped compound aggregates were observed at the center portion of the thickness of the above observation sample. The three titanium compounds observed were measured by EPMA. Perform line analysis in the thickness direction with the particles of the titanium compound as the center, and use the value of titanium in the inner layer as a reference to determine the concentration of the constituent elements (carbon, nitrogen, or oxygen) that are higher than those of the titanium compound, without particles The distance between the side regions was averaged to obtain the thickness of the diffusion layer of each of the stripe compound aggregates.
拉伸試驗係於鈦複合材之輥軋方向評估。抗拉速度係以至超過降伏點為止為0.4%/分鐘,超過降伏點 而始為30%/分鐘進行,據以測定強度。又,自降伏為止之應力-應變曲線之梯度求得楊氏模數。 The tensile test was performed on the rolling direction of the titanium composite. The tensile speed was measured at a rate of 0.4% / min until the fall point was exceeded, and 30% / min was exceeded when the fall point was exceeded, and the strength was measured. In addition, the Young's modulus was obtained from the gradient of the stress-strain curve until the drop.
結果彙總示於表1中。 The results are summarized in Table 1.
第7圖係Ti-0.1%N板之截面微組織之照片的一例。 Fig. 7 is an example of a photograph of a cross-section microstructure of a Ti-0.1% N plate.
如第7圖所例示,若觀察本發明例之試料No.8之鈦複合板的截面之組織,觀之呈黑狀之鈦化合物在各處可獲確認。此一黑色條狀化合物集合體為氮化鈦之集合體,X線繞射測定之結果,其為TiN。 As shown in FIG. 7, if the structure of the cross section of the titanium composite plate of the sample No. 8 of the example of the present invention is observed, the black titanium compound can be confirmed everywhere. This black strip compound assembly is an assembly of titanium nitride. As a result of X-ray diffraction measurement, it is TiN.
鈦中分散有選自碳化物、氮化物及氧化物之1種以上的鈦化合物之本發明例之試料No.1~8,與不具有此等鈦化合物之試料No.10相比,鈦複合材之強度與楊氏模數提升。又,於製作鈦捆包體5時,將鈦捆包體之內部之真空度設為較10Pa為大之試料No.9,其鈦複合材之內部部分氧化、強度降低,但楊氏模數維持於一定值以上。經添加TiO2粉末之No.2,氧之擴散層之厚度為4~6μm。經添加TiC粉末之No.4,其碳之擴散層之厚度為25~32μm。經添加TiN粉末之No.6,氮之擴散層之厚度為1~2μm。 Sample Nos. 1 to 8 of the present invention examples in which one or more titanium compounds selected from carbides, nitrides, and oxides are dispersed in titanium, compared with sample No. 10 in which no titanium compound is present Material strength and Young's modulus are improved. In the production of the titanium bale body 5, the vacuum degree inside the titanium bale body was set to sample No. 9 larger than 10 Pa. The titanium composite material was partially oxidized and the strength was reduced, but the Young's modulus Maintained above a certain value. After adding No. 2 of TiO 2 powder, the thickness of the oxygen diffusion layer is 4-6 μm. After TiC powder No. 4 is added, the thickness of the carbon diffusion layer is 25 to 32 μm. After adding TiN powder No. 6, the thickness of the nitrogen diffusion layer is 1 to 2 μm.
氧化物之粉末多量添加之試料No.11,熱軋時內部破裂發生,無法獲得堅實之鈦複合材。鈦捆包體5之壓下率小、內層部之空隙率大之試料No.12,氧化物與空隙均無方向性而點狀分布,於製作拉伸試驗片時破裂。 Sample No. 11 in which a large amount of oxide powder was added, internal cracking occurred during hot rolling, and a solid titanium composite material could not be obtained. In the sample No. 12 in which the rolling reduction of the titanium packing body 5 was small and the porosity of the inner layer portion was large, both the oxide and the voids were distributed in a point shape without directionality, and cracked when the tensile test piece was produced.
如表2所示,自鈦捆包體製造鈦複合材。 As shown in Table 2, a titanium composite material was produced from a titanium bundle.
作為填充材使用之海綿鈦,係由克羅爾法製 造之化學組成相當於JIS1種(C:0.001%、H:0.001%、O:0.04%、N:0.001%、Fe:0.03%、其餘部分Ti及雜質)之海綿鈦,海綿鈦B係使用粒度6mm以上且13mm以下者,海綿鈦C係使用粒度2.5mm以上且6mm以下者,海綿鈦D係使用粒度0.8mm以上且2.5mm以下者。 The sponge titanium used as a filler is a chemical composition equivalent to JIS1 (C: 0.001%, H: 0.001%, O: 0.04%, N: 0.001%, Fe: 0.03%, and the remainder) manufactured by the Kroll method. (Ti and impurities) sponge titanium, sponge titanium B is used with a particle size of 6mm to 13mm, sponge titanium C is used with a particle size of 2.5mm and 6mm or less, and sponge titanium D is used with a particle size of 0.8mm to 2.5mm.
又,作為鈦邊角料,部分(試料No.26,27)係使用JIS2種(C:0.002%、H:0.006%、O:0.08%、N:0.001%、Fe:0.05%、其餘部分Ti及雜質)之薄板切斷成10~20mm見方者。 In addition, as the titanium scrap, some (samples Nos. 26 and 27) are made of two types of JIS (C: 0.002%, H: 0.006%, O: 0.08%, N: 0.001%, Fe: 0.05%, and the rest of Ti and impurities ) Of the sheet is cut into 10 ~ 20mm square.
再者,作為填充材使用之鈦化合物等之粉末,係使用市售之TiO2粉末(平均粒徑2μm)、TiC粉末(平均粒徑3μm)或TiN粉末(平均粒徑5μm)。此等海綿鈦粒子與鈦化合物等之粉末,係以特定量投入V型混合器混合。 In addition, as a powder of a titanium compound or the like used as a filler, commercially available TiO 2 powder (average particle diameter of 2 μm), TiC powder (average particle diameter of 3 μm), or TiN powder (average particle diameter of 5 μm) is used. These sponge titanium particles and powders of titanium compounds are put into a V-type mixer for mixing in a specific amount.
作為捆包材之素材,工業用純鈦材係使用JIS1種(TP270H;C:0.002%、H:0.006%、O:0.04%、N:0.002%、Fe:0.03%、其餘部分Ti及雜質)、JIS2種(TP340H;C:0.001%、H:0.002%、O:0.10%、N:0.002%、Fe:0.06%、其餘部分Ti及雜質)、及Ti-0.06%Pd之經酸洗之厚度10mm的厚板。 As the material of the packing material, a pure titanium material for industrial use is JIS1 (TP270H; C: 0.002%, H: 0.006%, O: 0.04%, N: 0.002%, Fe: 0.03%, the rest of Ti and impurities) JIS2 (TP340H; C: 0.001%, H: 0.002%, O: 0.10%, N: 0.002%, Fe: 0.06%, the rest of Ti and impurities), and Ti-0.06% Pd's pickled thickness 10mm thick plate.
如第4圖所示,將工業用純鈦材之5片暫時組合,於其中填充海綿鈦粒子、或鈦邊角料與鈦化合物等之粉末之混合物(填充材),並以剩餘之工業用純鈦材的鈦捆包材封蓋之。 As shown in Fig. 4, five pieces of industrial pure titanium materials are temporarily combined, and sponge titanium particles or a mixture of titanium scraps and powders of titanium compounds (filling materials) are filled therein, and the remaining industrial pure titanium materials are filled. Titanium packaging material is used to cover it.
於此一狀態下,予以置入真空腔室內,減壓 (真空)至特定之壓力後,將捆包材之接縫以全周電子束熔接。此時之腔室內之壓力為9.5×10-3~2.1×10-1Pa。 In this state, it is placed in a vacuum chamber, and after the pressure is reduced (vacuum) to a specific pressure, the seams of the packing materials are welded by electron beams around the entire circumference. The pressure in the chamber at this time is 9.5 × 10 -3 to 2.1 × 10 -1 Pa.
依以上之方式,準備完成於內部填充有海綿鈦或鈦邊角料與鈦化合物等之粉末的混合物,且氛圍為真空之鈦捆包體。鈦捆包體之大小為厚度80×寬度100×長度120mm。 In the above manner, a titanium packing body filled with a sponge titanium or a titanium scrap material and a powder of a titanium compound and the like is prepared, and the atmosphere is a vacuum. The size of the titanium packing body is thickness 80 × width 100 × length 120 mm.
對於製作之鈦捆包體,於大氣氛圍下作850℃下6小時之加熱後,進行熱軋,製作厚度5mm之鈦複合板。而後,對於鈦複合材以725℃作15分鐘之退火後,予以酸洗除去表層之積垢後供於拉伸試驗。與實施例1相同地進行組織觀察與拉伸試驗,求得鈦複合材之空隙率、鈦化合物之形態與大小L/t、擴散層之厚度、強度及楊氏模數。 The produced titanium bundle was heated at 850 ° C. for 6 hours in an atmospheric atmosphere, and then hot-rolled to produce a titanium composite plate having a thickness of 5 mm. Then, the titanium composite material was annealed at 725 ° C for 15 minutes, and then acid-washed to remove scale on the surface layer, and then subjected to a tensile test. The structure observation and tensile test were performed in the same manner as in Example 1, and the porosity of the titanium composite material, the shape and size of the titanium compound L / t, the thickness, strength, and Young's modulus of the diffusion layer were obtained.
結果彙總示於表2中。 The results are summarized in Table 2.
於捆包材使用JIS2種之情形下,經添加鈦化合物粉末之本發明例的試料No.13~19,與未添加鈦化合物之試料No.20相比,鈦複合材之強度與楊氏模數提升。 In the case where two types of JIS are used for the packing material, the sample Nos. 13 to 19 of the example of the present invention in which titanium compound powder is added are compared with the sample No. 20 to which no titanium compound is added. Number of improvements.
又,鈦捆包體之壓下率小,內層部之空隙率變大之試料No.21,氧化物與空隙均無方向性而點狀分布,於製作拉伸試驗片時破裂。 In addition, in Sample No. 21, in which the rolling reduction of the titanium package was small and the porosity of the inner layer portion became large, both the oxide and the voids were distributed in a point shape without directionality, and cracked when the tensile test piece was produced.
捆包材使用JIS1種之情形下,經添加鈦化合物粉末之本發明例的試料No.22~24,與未添加鈦化合物之試料No.25相比,鈦複合材之強度與楊氏模數提升。 In the case of using JIS1 as the packing material, the sample No. 22 to 24 of the example of the present invention in which titanium compound powder is added has a strength and a Young's modulus of the titanium composite material compared to the sample No. 25 without the titanium compound added Promotion.
填充材使用氧量為0.08質量%之薄板邊角料的情形下,經添加鈦化合物粉末之本發明例的試料No.26,與未添加鈦化合物粉末之試料No.27相比,鈦複合材1之強度與楊氏模數提升。 In the case of using a sheet scrap with an oxygen content of 0.08% by mass as the filler, the sample No. 26 of the example of the present invention in which titanium compound powder was added was compared with the sample No. 27 in which titanium compound powder was not added. Increase in strength and Young's modulus.
捆包材使用JIS1種之情形下,與使用JIS2種之捆包材相比,可獲得加工性良好之鈦複合材1。捆包材6使用Ti-0.06%Pd之試料No.23,與使用JIS2種之捆包材6相比,可獲得耐蝕性良好之鈦複合材。又,經添加TiO2粉末之No.14,其氧之擴散層之厚度為2~6μm。經添加TiC粉末之No.16,其碳之擴散層之厚度為12~18μm。經添加TiN粉末之No.17,其氮之擴散層之厚度為1~2μm。 When a JIS 1 type of packaging material is used, a titanium composite material 1 having good processability can be obtained as compared with a JIS 2 type of packaging material. As the packing material 6, a sample No. 23 of Ti-0.06% Pd was used. Compared with the packing material 6 of JIS 2 type, a titanium composite material with good corrosion resistance was obtained. In addition, No. 14 in which TiO 2 powder was added had a thickness of the oxygen diffusion layer of 2 to 6 μm. After adding TiC powder No. 16, the thickness of the carbon diffusion layer is 12-18 μm. After TiN powder No. 17 is added, the thickness of the nitrogen diffusion layer is 1 to 2 μm.
將熱軋所得之表2所示的厚度5mm之鈦複合材即試料No.13、14、16、20,以725℃退火15分鐘後,予以 酸洗而除去表層之積垢。對於積垢除去之鈦複合(熱軋材),至到達1.0mm之厚度為止進行冷軋後,使用真空加熱爐以700℃作15分鐘之退火後供於拉伸試驗。與實施例1相同進行組織觀察與拉伸試驗,求取鈦複合材之空隙率、鈦化合物之形態與大小L/t、擴散層之厚度、強度及楊氏模數。 Samples Nos. 13, 14, 16, and 20 having a thickness of 5 mm shown in Table 2 obtained by hot rolling were annealed at 725 ° C for 15 minutes, and then acid-washed to remove scale deposits. The titanium composite (hot-rolled material) from which the scale was removed was cold-rolled until it reached a thickness of 1.0 mm, and then annealed at 700 ° C for 15 minutes using a vacuum heating furnace for a tensile test. The structure observation and tensile test were performed in the same manner as in Example 1. The porosity of the titanium composite material, the shape and size of the titanium compound L / t, the thickness and strength of the diffusion layer, and the Young's modulus were determined.
結果彙總於表3中。 The results are summarized in Table 3.
本發明例之試料No.28~30,藉由添加鈦化合物粉末,與未添加鈦化合物粉末之試料No.31相比,鈦複合材之強度與楊氏模數提升。又,經添加TiO2粉末之No.29,氧之擴散層之厚度為1~4μm。經添加TiC粉末之No.30,碳之擴散層之厚度為2~6μm。 In samples Nos. 28 to 30 of the examples of the present invention, by adding the titanium compound powder, compared with the sample No. 31 without adding the titanium compound powder, the strength and Young's modulus of the titanium composite are improved. In addition, the thickness of the oxygen diffusion layer was 1 to 4 μm by adding TiO 2 powder No. 29. After adding TiC powder No. 30, the thickness of the carbon diffusion layer is 2-6 μm.
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