WO2022158062A1 - 熱間プレス部材、塗装部材、熱間プレス用鋼板、および熱間プレス部材の製造方法ならびに塗装部材の製造方法 - Google Patents
熱間プレス部材、塗装部材、熱間プレス用鋼板、および熱間プレス部材の製造方法ならびに塗装部材の製造方法 Download PDFInfo
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- WO2022158062A1 WO2022158062A1 PCT/JP2021/039089 JP2021039089W WO2022158062A1 WO 2022158062 A1 WO2022158062 A1 WO 2022158062A1 JP 2021039089 W JP2021039089 W JP 2021039089W WO 2022158062 A1 WO2022158062 A1 WO 2022158062A1
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- WO
- WIPO (PCT)
- Prior art keywords
- less
- hot
- hot pressing
- steel sheet
- coating
- Prior art date
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- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 85
- 239000010959 steel Substances 0.000 title claims abstract description 85
- 238000000576 coating method Methods 0.000 title claims abstract description 62
- 239000011248 coating agent Substances 0.000 title claims abstract description 61
- 238000007731 hot pressing Methods 0.000 title claims abstract description 51
- 238000000034 method Methods 0.000 title claims abstract description 34
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 20
- 238000007747 plating Methods 0.000 claims description 66
- 238000010438 heat treatment Methods 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 15
- 229910052725 zinc Inorganic materials 0.000 claims description 13
- 229910052782 aluminium Inorganic materials 0.000 claims description 12
- 229910052742 iron Inorganic materials 0.000 claims description 11
- 230000009466 transformation Effects 0.000 claims description 9
- 238000005260 corrosion Methods 0.000 abstract description 33
- 230000007797 corrosion Effects 0.000 abstract description 31
- 239000010410 layer Substances 0.000 description 44
- 238000010422 painting Methods 0.000 description 30
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 18
- 239000011701 zinc Substances 0.000 description 17
- 235000019592 roughness Nutrition 0.000 description 14
- 238000005096 rolling process Methods 0.000 description 13
- 238000011282 treatment Methods 0.000 description 13
- 239000000126 substance Substances 0.000 description 11
- 230000000694 effects Effects 0.000 description 9
- 238000005275 alloying Methods 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000011247 coating layer Substances 0.000 description 7
- 238000004070 electrodeposition Methods 0.000 description 6
- 238000005098 hot rolling Methods 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 239000010960 cold rolled steel Substances 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- 238000009628 steelmaking Methods 0.000 description 5
- 230000003746 surface roughness Effects 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 238000005728 strengthening Methods 0.000 description 4
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 4
- 229910000165 zinc phosphate Inorganic materials 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000009713 electroplating Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000003303 reheating Methods 0.000 description 3
- 229910000859 α-Fe Inorganic materials 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229910001335 Galvanized steel Inorganic materials 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- 229910001566 austenite Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000007739 conversion coating Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000005485 electric heating Methods 0.000 description 2
- 239000008397 galvanized steel Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229910000765 intermetallic Inorganic materials 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- RRIWRJBSCGCBID-UHFFFAOYSA-L nickel sulfate hexahydrate Chemical compound O.O.O.O.O.O.[Ni+2].[O-]S([O-])(=O)=O RRIWRJBSCGCBID-UHFFFAOYSA-L 0.000 description 2
- 229940116202 nickel sulfate hexahydrate Drugs 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RZLVQBNCHSJZPX-UHFFFAOYSA-L zinc sulfate heptahydrate Chemical compound O.O.O.O.O.O.O.[Zn+2].[O-]S([O-])(=O)=O RZLVQBNCHSJZPX-UHFFFAOYSA-L 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910018125 Al-Si Inorganic materials 0.000 description 1
- -1 AlN nitrides Chemical class 0.000 description 1
- 229910018520 Al—Si Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910000611 Zinc aluminium Inorganic materials 0.000 description 1
- 229910007570 Zn-Al Inorganic materials 0.000 description 1
- 229910007567 Zn-Ni Inorganic materials 0.000 description 1
- 229910007614 Zn—Ni Inorganic materials 0.000 description 1
- PGTXKIZLOWULDJ-UHFFFAOYSA-N [Mg].[Zn] Chemical compound [Mg].[Zn] PGTXKIZLOWULDJ-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- HXFVOUUOTHJFPX-UHFFFAOYSA-N alumane;zinc Chemical compound [AlH3].[Zn] HXFVOUUOTHJFPX-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005261 decarburization Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000009503 electrostatic coating Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229910000734 martensite Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- QELJHCBNGDEXLD-UHFFFAOYSA-N nickel zinc Chemical compound [Ni].[Zn] QELJHCBNGDEXLD-UHFFFAOYSA-N 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C18/00—Alloys based on zinc
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C18/00—Alloys based on zinc
- C22C18/04—Alloys based on zinc with aluminium as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
- C22C21/02—Alloys based on aluminium with silicon as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/60—Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
- C23C2/06—Zinc or cadmium or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
- C23C2/12—Aluminium or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
Definitions
- the present invention relates to a hot pressed member, a coated member, a steel sheet for hot pressing, a method for manufacturing the hot pressed member, and a method for manufacturing the coated member.
- the present invention relates to a method for manufacturing a hot pressed member, a coated member, a steel plate for hot pressing, and a hot pressed member, and a method for manufacturing a coated member, which are excellent in post-painting clear image quality and post-painting corrosion resistance.
- Patent Document 1 discloses a steel sheet for hot pressing (hot-rolled steel sheet and cold-rolled steel sheet) coated with Al or an Al alloy that provides high strength and excellent corrosion resistance after hot pressing.
- Patent Document 2 discloses a hot press member having an ⁇ -Fe (Zn, Ni) mixed crystal, an intermetallic compound of Zn, Ni and Fe, and a layer containing Mn.
- JP-A-2000-38640 Japanese Patent Application Publication No. 2013-503254
- the hot-pressed members disclosed in Patent Documents 1 and 2 are both hot-pressed members manufactured by heating plated steel sheets, and are excellent in corrosion resistance after painting, but have no clear image after painting. not cared for.
- the present invention has been made in view of the above problems, and an object of the present invention is to provide a hot pressed member and a coated member that are excellent in post-coating clear image and post-coating corrosion resistance, and a method for manufacturing them. Another object of the present invention is to provide a steel sheet for hot pressing which is suitable for hot pressing members and has excellent post-painting clear image and post-painting corrosion resistance.
- the present inventors have conducted intensive research and obtained the following findings.
- (1) In order to improve the sharpness of the hot pressed member after painting, it is effective to set the filtered center line waviness Wca of the surface to 1.5 ⁇ m or less. Further, by setting the line roughness Ra to 2.0 ⁇ m or less and the skewness Rsk to 0 or less, a further improvement in sharpness after painting can be expected.
- (2) By setting the filtered center line waviness Wca of the steel sheet for hot pressing before hot pressing to 0.75 ⁇ m or less, the filtered center line waviness Wca after hot pressing can be set to 1.5 ⁇ m or less. It is possible.
- a hot press member having a filtered center line waviness Wca of at least one surface of 1.5 ⁇ m or less.
- a coated member comprising the hot pressed member according to any one of [1] to [3] as a base material, and having a coating film layer having a thickness of 15 ⁇ m or more on at least one surface of the base material. .
- a steel sheet for hot press having a filtered center line waviness Wca of at least one surface of 0.75 ⁇ m or less.
- the line roughness Ra of the at least one surface is 1.0 ⁇ m or less, and the crack density per unit cross-sectional length in an arbitrary 1 mm-long cross section of the at least one surface is 30 locations/mm or more.
- a steel plate for hot press having a filtered center line waviness Wca of at least one surface of 0.75 ⁇ m or less is heated to a temperature range from the Ac 3 transformation point to 1000 ° C. and hot pressed, and then the thickness
- a hot pressed member that is excellent in post-coating clear image and post-coating corrosion resistance.
- a coated member that is excellent in clear image after coating and is suitable for automotive exterior panel parts.
- it is possible to provide a steel sheet for hot pressing that is suitable for hot pressing members that are excellent in post-painting clear image and post-painting corrosion resistance.
- the inventors diligently studied methods for improving the quality of the painted appearance of hot pressed parts.
- the sharpness after painting of the hot-pressed parts is closely related to the surface roughness of the hot-pressed parts
- the surface roughness of the hot-pressed parts is closely related to the surface roughness and surface separation of the hot-pressed steel plate. confirmed to be closely related to the state.
- plating mainly composed of Al or Zn to a steel sheet for hot press, a hot press member having excellent corrosion resistance after coating can be obtained.
- the hot press member of the present invention has a filtered centerline waviness Wca of at least one surface of 1.5 ⁇ m or less.
- Wca which corresponds to long-wavelength unevenness, remains even after a thick coating is applied, and is directly linked to the appearance quality after coating.
- the filtered center line waviness Wca is preferably 1.4 ⁇ m or less, and more preferably 1.3 ⁇ m or less.
- the line roughness Ra of the surface where the filtered center line waviness Wca is 1.5 ⁇ m or less is 2.0 ⁇ m or less and the skewness Rsk is 0 or less.
- Ra which corresponds to short-wavelength irregularities, is buried in the coating film, so that it has less influence than Wca, but it is desirable to reduce it from the viewpoint of obtaining more excellent image sharpness after painting.
- Ra is 1.8 ⁇ m or less, more preferably 1.5 ⁇ m or less, and most preferably 1.0 ⁇ m or less.
- the lower limit if Ra is less than 0.2 ⁇ m, surface flaws may become conspicuous and the surface quality may be impaired, so Ra is preferably 0.2 ⁇ m or more.
- the skewness Rsk is the ratio of the height of the peak and the depth of the valley (the height of the peak/the depth of the valley), which is a roughness form factor that indicates the size and shape of the peak and valley of fine unevenness (roughness). depth).
- this value has a positive (+) value
- the height of the peak is greater than the depth of the valley
- if it has a negative (-) value the height of the peak is greater than the depth of the valley.
- Rsk By setting Rsk to a negative value, a high glossiness and excellent coating film quality can be obtained. This is probably because when Rsk has a negative value, there are many flat peaks and the proportion of specularly reflected light increases.
- the skewness Rsk is 0 or less.
- the skewness Rsk is more preferably -0.3 or less, and even more preferably -0.5 or less.
- Rsk is preferably -1.0 or more.
- the hot press member of the present invention contains one or more selected from Al, Zn, and Fe on the surface side where the filtered center line waviness Wca is 1.5 ⁇ m or less, and has a thickness of 10 ⁇ m to 80 ⁇ m. It is preferable to have a plated layer. Regardless of the presence or absence of plating, at least one surface of the hot press member of the present invention has a filtered center line waviness Wca of 1.5 ⁇ m or less and a line roughness Ra of that surface of 2.0 ⁇ m or less. , skewness Rsk of 0 or less.
- the speed of corrosion is reduced, resulting in excellent coating.
- the film appearance can be maintained for a long period of time.
- the speed of crevice corrosion (joint corrosion) at the joint where the coating does not follow is also reduced, and the perforation corrosion life of the member can be extended.
- Examples of plating layers containing one or more selected from Al, Zn, and Fe include Al-based plating layers and Zn-based plating layers.
- Al-based plating layer Fe: 10 to 90%, Si: 1 to 15%, Mg: 0 to 10% (including 0), Ca: 0 to 10% (including 0), Zn: 0 to 50 % (including 0) with the balance being Al and unavoidable impurities.
- Fe 10 to 90%, Al: 0 to 20% (including 0), Mg: 0 to 10% (including 0), Ca: 0 to 10% (including 0 ), Ni: 0 to 30% (including 0), Co: 0 to 30% (including 0), Mn: 0 to 30% (including 0), Cr: 0 to 30% (including 0) containing Zn and the remainder consisting of Zn and unavoidable impurities are exemplified.
- the plating layer preferably has a thickness of 10 ⁇ m or more. More preferably, the thickness of the plating layer is 20 ⁇ m or more. On the other hand, even if the thickness of the plating layer is excessively increased, the effect of improving the corrosion resistance is saturated, and the manufacturing cost only increases.
- the thickness of the plating layer is more preferably 50 ⁇ m or less, and even more preferably 30 ⁇ m or less.
- the coated member of the present invention has the aforementioned hot pressed member as a base material, and has a coating film layer having a thickness of 15 ⁇ m or more on at least one surface.
- the surface on which the coating layer is formed is the surface of the hot pressed member on which the filtered center line waviness Wca is 1.5 ⁇ m or less. If there is a plating layer, a coating layer is formed on the plating layer or the chemical conversion coating of the hot pressed member, and if there is no plating layer, a coating is formed on the hot pressing member or the chemical conversion coating. forming layers.
- a thicker coating layer provides better appearance quality.
- the total thickness of the coating layer on one side is preferably 40 ⁇ m or more, more preferably 80 ⁇ m or more. Even if the thickness of the coating film layer is excessively increased, the effect of improving the appearance is saturated and the cost only increases, so the total thickness of the coating film layer is preferably 150 ⁇ m or less, more preferably 120 ⁇ m in total Below.
- Examples of resins contained in the coating layer include epoxy resins, melamine resins, acrylic resins, alkyd resins, polyester resins, acrylic resins, and urethane resins. A composite resin of these may also be used. Moreover, such a coating film layer may be only one layer, or a plurality of layers of two or more layers may be formed.
- the thickness of the coating layer can be measured by observing the cross section of the coated member with an optical microscope or scanning electron microscope (SEM).
- SEM scanning electron microscope
- the coating film can be clearly observed under the scanning electron microscope observation conditions, for example, when the acceleration voltage is 15 kV and the magnification of the secondary electron image is 200 times or more.
- chemical conversion treatment may be applied as a pretreatment for painting.
- chemical conversion treatment it is possible to hope to improve the adhesion between the base material and the coating film.
- chemical conversion treatments include zinc phosphate-based chemical conversion treatments and zirconium oxide-based chemical conversion treatments.
- the steel plate for hot press of the present invention has a filtered center line waviness Wca of 0.75 ⁇ m or less on at least one surface.
- Wca of the steel sheet for hot press is preferably 0.60 ⁇ m or less, more preferably 0.50 ⁇ m or less, still more preferably 0.30 ⁇ m or less, and most preferably 0, from the viewpoint of obtaining a better appearance after heat treatment and painting. .20 ⁇ m or less.
- the method of controlling the waviness of the steel sheet for hot press is not particularly limited, but a method such as adjustment of the rolls in temper rolling of the steel sheet after rolling or after plating is exemplified.
- the steel sheet for hot press of the present invention has a line roughness Ra of 1.0 ⁇ m or less on the surface where the filtered center line waviness Wca is 0.75 ⁇ m or less, and a unit cross section of an arbitrary 1 mm length cross section of the surface It is preferable that the crack density per length is 30 locations/mm or more. As with Wca described above, Ra also increases about twice due to alloying in hot pressing. By setting the Ra of the steel sheet for hot pressing to 1.0 ⁇ m or less, the Ra after hot pressing can be stably 2.0 ⁇ m or less.
- the Ra of the steel sheet for hot press is more preferably 0.75 ⁇ m, still more preferably 0.5 ⁇ m or less, and most preferably 0.3 ⁇ m or less.
- the method for controlling the Ra of the steel sheet for hot press is not particularly limited, but a method such as adjustment of rolls in temper rolling of the steel sheet after rolling or after plating is exemplified.
- the crack density per unit cross-sectional length in an arbitrary cross section of 1 mm length to 30 locations/mm or more.
- the crack density is more preferably 50 locations/mm or higher, still more preferably 70 locations/mm or higher, and most preferably 80 locations/mm or higher.
- the method of forming cracks on the surface of the steel sheet for hot pressing is not particularly limited, but examples include applying tensile stress (tensile working), laser damage, and dissolution of grain boundaries by chemical treatment such as acid immersion.
- plating on the steel sheet for hot press is not essential, and non-plated steel sheet can be used when manufacturing hot press members applied to parts that do not require corrosion resistance.
- one or more selected from Al, Zn, and Fe is added to the surface side where the filtered center line waviness Wca is 0.75 ⁇ m or less. It is desirable to have a containing plating layer.
- the metal forming the plated layer may be pure zinc, pure aluminum, or an alloy thereof, or may contain other alloying elements. For example, by containing 0.1 to 20% of an element selected from Mg, Cr, Co, and Ni, further improvement in corrosion resistance can be expected.
- the plating layer may be one in which oxides are dispersed, and examples include those containing 0.1 to 10% of nanoparticles of SiO 2 or Al 2 O 3 .
- the thickness of the plating layer is not limited, it is preferably 3 ⁇ m or more, more preferably 6 ⁇ m or more, and even more preferably 10 ⁇ m or more in order to exhibit corrosion resistance after heat treatment. In order to complete alloying in the hot stamping process, the thickness of the plating layer is preferably 30 ⁇ m or less, more preferably 20 ⁇ m or less.
- at least one surface of the steel sheet for hot press of the present invention has a filtered center line waviness Wca of 0.75 ⁇ m or less and a line roughness Ra of 1.0 ⁇ m.
- the crack density per unit cross-sectional length in an arbitrary cross section of 1 mm length is 30 locations/mm or more.
- the plating layer of the present invention may be a single-layer plating layer, but a lower layer coating or an upper layer coating may be provided depending on the purpose, as long as the effects of the present invention are not affected.
- an underlying plating layer mainly composed of Ni is exemplified as the underlayer coating.
- the steel plate for hot pressing in order to obtain a hot pressed member that exceeds 1470 MPa class after hot pressing, should contain, for example, C: 0.20 to 0.50%, Si : 0.1-0.5%, Mn: 1.0-3.0%, P: 0.02% or less, S: 0.01% or less, Al: 0.10% or less, N: 0.01 % or less, with the balance being Fe and unavoidable impurities.
- the steel sheet may be either a cold-rolled steel sheet or a hot-rolled steel sheet. The reason for limitation of each component is described below.
- C 0.20-0.50% C improves strength by forming martensite or the like as a steel structure. 0.20% or more is necessary to obtain strength exceeding 1470 MPa class. Therefore, it is preferable that the amount of C is 0.20% or more. More preferably, the amount of C is 0.22% or more. On the other hand, if it exceeds 0.50%, the toughness of the spot welded portion is lowered. Therefore, the amount of C is preferably 0.50% or less. The C content is more preferably 0.45% or less, even more preferably 0.43% or less, and most preferably 0.40% or less.
- Si 0.1-0.5% Si is an effective element for strengthening steel and obtaining a good quality.
- the amount of Si is required to be 0.1% or more. Therefore, the Si content is preferably 0.1% or more. More preferably, the amount of Si is 0.2% or more. On the other hand, if it exceeds 0.5%, ferrite is stabilized, so that hardenability is lowered. Therefore, the Si content is preferably 0.5% or less.
- the Si content is more preferably 0.4% or less, more preferably 0.3% or less.
- Mn 0.5-3.0%
- Mn is an effective element for ensuring strength after cooling in a wide cooling rate range. In order to ensure mechanical properties and strength, it is necessary to contain 0.5% or more. Therefore, the Mn content is preferably 0.5% or more. The Mn content is more preferably 0.7% or more, more preferably 1.0% or more. On the other hand, if it exceeds 3.0%, not only the cost rises but also the effect saturates. Therefore, the Mn content is preferably 3.0% or less. The Mn content is more preferably 2.5% or less, even more preferably 2.0% or less, and most preferably 1.5% or less.
- the amount of P is 0.1% or less.
- the P content is preferably 0.01% or more.
- S 0.01% or less S becomes inclusions such as MnS and causes deterioration of impact resistance and cracks along the metal flow of the weld. Therefore, it is desirable to reduce it as much as possible, preferably 0.01% or less. Further, in order to ensure good stretch flangeability, the content is more preferably 0.005% or less, more preferably 0.001% or less. Note that the lower limit is preferably 0.0002% or more from the viewpoint of steelmaking costs.
- the Al content is preferably 0.10% or less.
- the Al content is more preferably 0.07% or less, more preferably 0.04% or less.
- the Al content is preferably 0.01% or more from the viewpoint of securing the effect as a deoxidizer.
- the N content is preferably 0.01% or less. From the viewpoint of steelmaking costs, the N content is preferably 0.001% or more.
- Nb 0.10% or less
- Ti 0.05% or less
- B 0.0002 to 0.005 %
- Cr 0.1 to 0.3%
- Sb 0.003 to 0.03%
- Nb 0.10% or less
- Nb is a component effective in strengthening steel, but if it is included in excess, the rolling load increases. Therefore, when Nb is contained, the amount of Nb should be 0.10% or less, preferably 0.05% or less. Note that the lower limit is preferably 0.005% or more from the viewpoint of steelmaking costs.
- Ti 0.05% or less Ti, like Nb, is also effective in strengthening steel, but there is a problem that if it is contained excessively, shape fixability is lowered. Therefore, when Ti is contained, the amount of Ti should be 0.05% or less, preferably 0.03% or less. Note that the lower limit is preferably 0.003% or more from the viewpoint of steelmaking cost.
- B 0.0002 to 0.005% B has the effect of suppressing the formation and growth of ferrite from austenite grain boundaries, so it is preferably contained in an amount of 0.0002% or more. Therefore, when the amount of B is contained, the amount of B is preferably 0.0002% or more, more preferably 0.0010% or more. On the other hand, excessive B content greatly impairs moldability. Therefore, when B is contained, the amount of B is 0.005% or less, preferably 0.003% or less.
- Cr 0.1-0.3% Cr is useful for strengthening steel and improving hardenability. It is preferable to contain 0.1% or more in order to express such an effect. Therefore, when Cr is contained, the Cr content should be 0.1% or more, preferably 0.2% or more. On the other hand, since the alloy cost is high, the content exceeding 0.3% causes a significant increase in cost. Therefore, when Cr is contained, it should be 0.3% or less, preferably 0.2% or less.
- Sb 0.003-0.03%
- Sb has the effect of suppressing decarburization of the surface layer of the steel sheet in the annealing process of the base sheet for plating. In order to exhibit such an effect, it is necessary to contain 0.003% or more. Therefore, when Sb is contained, the Sb content should be 0.003% or more, preferably 0.005% or more. On the other hand, if the Sb content exceeds 0.03%, the rolling load is increased, which lowers the productivity. Therefore, when Sb is contained, the amount of Sb is 0.03% or less, preferably 0.02% or less, and more preferably 0.01% or less.
- the balance other than the above consists of Fe and unavoidable impurities.
- the tensile strength of the hot pressed member preferably exceeds 1320 MPa, more preferably exceeds 1400 MPa, and further preferably exceeds 1470 MPa.
- the rolling end temperature in hot rolling is equal to or higher than the Ar 3 transformation point in consideration of productivity and plate thickness accuracy. Cooling after hot rolling is performed by a normal method, but the coiling temperature at that time is preferably 550 ° C. or higher from the viewpoint of productivity. is desirably set to 750° C. or lower. Pickling and cold rolling may be carried out by conventional methods.
- the subsequent plating film formation method is not limited, and is appropriately selected according to the alloy system.
- Pure zinc or zinc-nickel alloy plating is preferably formed by electroplating, and zinc-aluminum alloy plating is preferably formed by hot dipping.
- Zinc-magnesium alloy plating is preferably formed by vacuum deposition.
- Al--Si based plating is preferably formed by a hot dipping method.
- plating can be performed under normal conditions in both continuous plating equipment with a non-oxidizing furnace and continuous plating equipment without a non-oxidizing furnace, and special control is required only for this steel sheet. It does not impede productivity because it does not
- the heating temperature of the steel sheet for hot pressing is lower than the Ac 3 transformation point, it may not be possible to obtain the strength required as a hot pressing member. Therefore, the heating temperature should be above the Ac 3 transformation point.
- the heating temperature is preferably 860° C. or higher. If the heating temperature exceeds 1000° C., the oxide film formed by oxidizing the base material and the plating layer becomes excessively thick, which may deteriorate the adhesion of the paint on the resulting hot pressed member. . Therefore, the heating temperature should be 1000° C. or less.
- the heating temperature is preferably 950° C. or lower, more preferably 900° C. or lower.
- the rate of temperature increase is preferably 3° C./sec or more and 300° C./sec or less.
- the heating rate is preferably 3° C./sec or higher, more preferably 10° C./sec or higher, and even more preferably 50° C./sec or higher.
- the heating rate is preferably 300° C./sec or less, more preferably 250° C./sec or less, and even more preferably 200° C./sec or less.
- the holding time at the above heating temperature is not limited at all.
- the holding time is set to 5 minutes or less. preferably within 3 minutes, more preferably within 1 minute.
- the method for heating the steel sheet for hot press is not limited at all, and examples thereof include furnace heating using an electric furnace or gas furnace, electric heating, induction heating, high-frequency heating, and flame heating.
- hot press working is performed, and at the same time or immediately after working, a hot press member is manufactured by cooling using a mold or a coolant such as water.
- hot pressing conditions are not particularly limited, but pressing can be carried out at a general hot pressing temperature range of 600 to 800°C.
- a coated steel sheet for hot press having a filtered center line waviness Wca of at least one surface of 0.75 ⁇ m or less is heated to a temperature range of from the Ac 3 transformation point to 1000 ° C.
- a coating film layer having a thickness of 15 ⁇ m or more after hot pressing a coated member having excellent appearance quality can be produced.
- the coating method is not limited, a suitable method can be selected according to the type of coating used, and examples thereof include cationic electrodeposition coating, electrostatic coating and spray coating.
- Al-based plating was applied to the base steel sheet by the following hot-dip plating method.
- Zn-based plating was applied by a hot-dip plating method or an electroplating method described below.
- non-plated steel sheets were also prepared as steel sheets for hot press that were not plated (Level Nos. 23 and 24).
- Hot-dip plating method The cold-rolled steel sheet is immersed in a hot-dip Al—Si-based or hot-dip Zn—Al-based plating bath by a hot-dip plating equipment, and then N 2 gas wiping is performed to obtain the level No. 1 in Table 1. 1-7 and no. Plated steel sheets for hot pressing No. 13 to 18 were produced.
- the cold-rolled steel sheet is immersed in a hot-dip Zn plating bath by hot-dip plating equipment, then N 2 gas wiping is performed, and then alloying treatment is performed in a direct electric heating furnace. . 8 to 12 plated steel sheets for hot press were produced.
- Wca and Ra were changed by performing temper rolling with rolls having various roughnesses.
- the current density is set to 10 to 10.
- the surface of the plated steel sheet was cracked by stretching or immersion in an acid solution.
- the tensile working was performed by uniaxially stretching the steel sheet for hot pressing in the rolling direction at an elongation rate of 5%.
- the immersion in the acid solution was carried out by immersing the plated steel sheet in an aqueous solution with a pH of 1.4 and a bath temperature of 50°C consisting of 115 g/L of zinc sulfate heptahydrate, 230 g/L of nickel sulfate hexahydrate, and 55 g/L of sodium sulfate. It was carried out by immersing in for 40 seconds.
- the above-mentioned steel sheets for hot pressing with plating and steel sheets for hot pressing without plating were subjected to hot pressing.
- a test piece of 100 mm ⁇ 200 mm was taken from the obtained steel sheet for hot press, and heat-treated in an electric furnace.
- Table 1 shows the heat treatment conditions (heating temperature, holding time). After the heat treatment, the test piece was taken out from the electric furnace and immediately hot-pressed using a hat-type mold at a molding start temperature of 700° C. to obtain a hot-pressed member.
- the shape of the obtained hot press member was 100 mm long on the upper flat portion, 50 mm long on the side flat portion, and 50 mm long on the lower flat portion.
- the bending R of the mold is 7R for both shoulders of the upper surface and both shoulders of the lower surface.
- a test piece of 70 mm ⁇ 150 mm was cut from the flat part of the upper surface of the obtained hot pressed member, and the geometric shape of the surface (filtered center line waviness Wca, line roughness Ra, skewness Rsk), clear image after painting and corrosion resistance after painting. Note that the non-plated steel sheet No. For Nos. 23 and 24, the iron scale was removed by shot blasting, the surface roughness was measured, and then painting was performed.
- an intermediate coating (TP65P manufactured by Kansai Paint Co., Ltd.) and a top coating (Neo Aramic 6000-4) are applied on top of this so that the total thickness of the coating and the electrodeposition coating is 80 ⁇ m. It was used for evaluation of post-corrosion resistance.
- the surface geometry (filtered centerline waviness Wca, line roughness Ra, skewness Rsk) was measured according to JIS B0601 using Surfcom 1500SD3 manufactured by Tokyo Seimitsu. Surface geometry measurements were made on hot pressed parts on the surface to which the intermediate and topcoats were applied. When intermediate coating and top coating were applied on both sides, the measurement was performed on both sides. As for the steel sheets for hot pressing, the surface to which the intermediate coating and top coating were applied after hot pressing was measured. When intermediate coating and top coating were applied to both sides, the measurement was performed on both sides.
- SAE-J2334 A hot press member subjected to zinc phosphate conversion treatment, electrodeposition coating and 3-coat coating was subjected to a corrosion test (SAE-J2334) to evaluate the state of
- the maximum swelling width on one side from the cross-cut was measured and judged according to the following criteria.
- Table 1 shows the evaluation results. ⁇ (passed, particularly excellent): maximum swelling width on one side ⁇ 1.5 mm ⁇ (passed, better): 1.5 mm ⁇ maximum swelling width on one side ⁇ 3.0 mm ⁇ (accepted): 3.0 mm ⁇ maximum swelling width on one side ⁇ 4.0 mm ⁇ (failed): 4.0 mm ⁇ maximum swelling width on one side
- the hot pressed member of the present invention is excellent in clear image after painting and corrosion resistance after painting. Moreover, by using the hot pressed member of the present invention as a base material, it is possible to obtain a coated member which is excellent in clear image after coating and corrosion resistance after coating. Further, with the steel sheet for hot press use of the present invention, it is possible to obtain a hot press member that is excellent in after-painting clear image and post-painting corrosion resistance.
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Abstract
Description
(1)熱間プレス部材の塗装後鮮映性を向上させるためには、その面のろ波中心線うねりWcaを1.5μm以下とすることが有効である。また、線粗さRaを2.0μm以下、スキューネスRskを0以下とすることで、塗装後鮮映性のより一層の向上を見込むことができる。
(2)熱間プレス前の熱間プレス用鋼板のろ波中心線うねりWcaを0.75μm以下とすることで、熱間プレス後のろ波中心線うねりWcaを1.5μm以下とすることが可能である。
[1]少なくとも一方の面のろ波中心線うねりWcaが1.5μm以下である、熱間プレス部材。
[2]前記少なくとも一方の面の線粗さRaが2.0μm以下、スキューネスRskが0以下である、[1]に記載の熱間プレス部材。
[3]前記少なくとも一方の面に、Al、Zn、Feから選択される1種以上を含有し、厚さが10~80μmであるめっき層を有する、[1]または[2]に記載の熱間プレス部材。
[4][1]~[3]のいずれかに記載の熱間プレス部材を基材とし、前記基材の少なくとも一方の面に、厚さが15μm以上である塗膜層を有する、塗装部材。
[5]少なくとも一方の面のろ波中心線うねりWcaが0.75μm以下である、熱間プレス用鋼板。
[6]前記少なくとも一方の面の線粗さRaが1.0μm以下であり、かつ前記少なくとも一方の面の任意の1mm長さの断面における単位断面長さ当たりのクラック密度が30箇所/mm以上である、[5]に記載の熱間プレス用鋼板。
[7]前記少なくとも一方の面に、Al、Zn、Feから選択される1種以上を含有し、厚さが3~30μmであるめっき層を有する、[5]または[6]に記載の熱間プレス用鋼板。
[8]少なくとも一方の面のろ波中心線うねりWcaが0.75μm以下である熱間プレス用鋼板を、Ac3変態点~1000℃の温度範囲に加熱後熱間プレスする、熱間プレス部材の製造方法。
[9]少なくとも一方の面のろ波中心線うねりWcaが0.75μm以下である熱間プレス用鋼板を、Ac3変態点~1000℃の温度範囲に昇温し熱間プレスしたのち、厚さが15μm以上である塗膜層を設ける、塗装部材の製造方法。
まず、本発明の熱間プレス部材の表面の幾何学的形状について説明する。本発明の熱間プレス部材は、少なくとも一方の面のろ波中心線うねりWcaが1.5μm以下である。長波長の凹凸に対応するWcaは、厚い塗装を施したのちも残存し、塗装後の外観品質に直結することから、各種幾何学パラメータの中でも鮮映性への影響が大きい。Wcaを低減させることによって、所定の外観特性を得るために必要な塗料の厚みを小さくすることができる。あるいは、一定の厚みの塗膜について、塗装後外観の品質を向上させることができる。好ましくはろ波中心線うねりWcaが1.4μm以下であり、より好ましくはろ波中心線うねりWcaが1.3μm以下である。なお、下限については、Wcaを0.1μm未満とするためには結晶粒を極めて微細にする必要があり、コスト高となるという理由からWcaは0.1μm以上とすることが好ましい。
本発明の塗装部材は、前述の熱間プレス部材を基材とし、少なくとも一方の面に、厚さが15μm以上である塗膜層を有する。塗膜層が形成される面は、熱間プレス部材における、ろ波中心線うねりWcaが1.5μm以下である面とする。めっき層がある場合には、熱間プレス部材のめっき層もしくは化成処理皮膜の上に塗膜層を形成させ、めっき層が無い場合には熱間プレス部材もしくは化成処理皮膜の上に、塗膜層を形成させている。塗膜層を厚くすることで、より優れた外観品質を得られる。塗膜層の厚さは、好ましくは一方の面の合計で40μm以上、さらに好ましくは合計で80μm以上とする。塗膜層の厚さを過剰に大きくしても外観改善効果は飽和し、コスト増となるのみであることから、塗膜層の厚さは好ましくは合計で150μm以下、さらに好ましくは合計で120μm以下とする。
本発明の熱間プレス用鋼板は、少なくとも一方の面のろ波中心線うねりWcaが0.75μm以下とする。めっきを施された熱間プレス用鋼板を用いる場合、めっき成分と母材のFeの相互拡散により合金化が進行し、加熱後の実質的なめっき厚さは加熱前のめっき厚さより大きくなる。本発明者らの検討では、このときのめっき厚さの増分はめっき組成に依存し、最大で3倍程度であるが、面内に分布を有し、厚さがほとんど増大しない箇所も存在することが分かっており、これがうねりの増大に寄与していると推定している。このとき、めっき厚の増大した箇所と厚さの変化しない箇所の間で、元の厚さの2倍のムラを生じることとなる。また、めっき層を有していない非めっき鋼板の場合は、熱処理により表面にスケールが生じる。スケールの厚さは熱処理条件により変化し、面内に分布を有する場合があり、その結果、熱処理前と比較しうねりが増大するおそれがある。本発明では、熱間プレス用鋼板のうねりを0.75μm以下とすることで、熱間プレス後のうねりを安定的に1.5μm以下とすることができる。より優れた熱処理および塗装後の外観を得るという観点で、熱間プレス用鋼板のWcaは好ましくは0.60μm以下、より好ましくは0.50μm以下、さらに好ましくは0.30μm以下、もっとも好ましくは0.20μm以下とする。なお、下限については、Wcaを0.01μm未満とするためには結晶粒を極めて微細にする必要があり、コスト高となるという理由からWcaは0.01μm以上とすることが好ましい。
Cは、鋼組織としてマルテンサイトなどを形成させることで強度を向上させる。1470MPa級を超えるような強度を得るためには0.20%以上必要である。したがって、C量は0.20%以上とすることが好ましい。C量は0.22%以上とすることがより好ましい。一方、0.50%を超えるとスポット溶接部の靱性が低下する。したがって、C量は0.50%以下とすることが好ましい。C量は0.45%以下とすることがより好ましく、0.43%以下とすることがさらに好ましく、0.40%以下とすることがもっとも好ましい。
Siは鋼を強化して良好な材質を得るのに有効な元素である。そのためにはSi量は0.1%以上必要である。したがって、Si量は0.1%以上とすることが好ましい。Si量は0.2%以上とすることがより好ましい。一方、0.5%を超えるとフェライトが安定化されるため、焼き入れ性が低下する。したがって、Si量は0.5%以下とすることが好ましい。Si量は0.4%以下とすることがより好ましく、0.3%以下とすることがさらに好ましい。
Mnは冷却後の強度確保を広い冷却速度範囲で得るために有効な元素である。機械特性や強度を確保するためは0.5%以上含有させることが必要である。したがって、Mn量は0.5%以上とすることが好ましい。Mn量は0.7%以上とすることがより好ましく、1.0%以上とすることがさらに好ましい。一方、3.0%超えると、コストが上昇するばかりでなく効果は飽和する。したがって、Mn量は3.0%以下とすることが好ましい。Mn量は2.5%以下とすることがより好ましく、2.0%以下とすることがさらに好ましく、1.5%以下とすることがもっとも好ましい。
P量が0.1%を超えると鋳造時のオーステナイト粒界へのP偏析に伴う粒界脆化により、局部延性の劣化を通じて強度と延性のバランスが低下する。したがって、P量は0.1%以下とすることが好ましい。また、製鋼コストの観点から、P量は0.01%以上とすることが好ましい。
SはMnSなどの介在物となって、耐衝撃性の劣化や溶接部のメタルフローに沿った割れの原因となる。したがって、極力低減することが望ましく0.01%以下とすることが好ましい。また、良好な伸びフランジ性を確保するため、より好ましくは0.005%以下とし、さらに好ましくは0.001%以下とする。なお、下限については、製鋼コストの観点から0.0002%以上とすることが好ましい。
Al量が0.1%を超えると、素材の鋼板のブランキング加工性や焼入れ性を低下させる。したがって、Al量は0.10%以下とすることが好ましい。Al量は0.07%以下とすることがより好ましく、0.04%と以下とすることがさらに好ましい。なお、下限については、脱酸材としての効果を確保する観点から、Al量は0.01%以上とすることが好ましい。
N量が0.01%を超えると、熱間圧延時や熱間プレス前の加熱時にAlNの窒化物を形成し、素材の鋼板のブランキング加工性や焼入れ性を低下させる。したがって、N量は0.01%以下とすることが好ましい。製鋼コストの観点から、N量は0.001%以上とすることが好ましい。
Nbは鋼の強化に有効な成分であるが、過剰に含まれると圧延荷重が増大する。したがって、Nbを含有させる場合は、Nb量は0.10%以下とし、好ましくは0.05%以下とする。なお、下限については、製鋼コストの観点から0.005%以上とすることが好ましい。
TiもNbと同様に鋼の強化には有効であるが、過剰に含まれると形状凍結性が低下するという課題がある。したがって、Tiを含有させる場合は、Ti量は0.05%以下とし、好ましくは0.03%以下とする。なお、下限については、製鋼コストの観点から0.003%以上とすることが好ましい。
Bはオーステナイト粒界からのフェライト生成および成長を抑制する作用を有するため、0.0002%以上含有することが好ましい。したがって、B量を含有させる場合には、B量は0.0002%以上とすることが好ましく、0.0010%以上とすることがより好ましい。一方、過剰なBの含有は成形性を大きく損なう。したがって、Bを含有させる場合は、B量は0.005%以下とし、好ましくは0.003%以下とする。
Crは鋼の強化および焼き入れ性を向上させるために有用である。このような効果を発現するためには0.1%以上含有することが好ましい。したがって、Crを含有する場合には、Cr含有量は0.1%以上とし、好ましくは0.2%以上とする。一方、合金コストが高いため0.3%超えの含有は大幅なコストアップを招く。したがって、Crを含有させる場合は0.3%以下とし、好ましくは0.2%以下とする。
Sbはめっき用原板の焼鈍工程で、鋼板表層の脱炭を抑止する効果がある。このような効果を発現するためには0.003%以上含有することが必要である。したがって、Sbを含有する場合には、Sb含有量は0.003%以上とし、好ましくは0.005%以上とする。一方、Sb量が0.03%を超えると圧延荷重の増加を招くため生産性を低下させる。したがって、Sbを含有させる場合は、Sb量は0.03%以下とし、好ましくは0.02%以下、より好ましくは0.01%以下とする。
本発明の鋼板の製造条件については特に規定しないが、以下に望ましい製造条件について説明する。前述したような成分の鋼を鋳造し、得られた熱片スラブを直接または加熱した後、あるいは冷片を再加熱して熱間圧延を施す。その際、熱片スラブを直接圧延することと再加熱後に圧延することでの特性変化はほとんど認められない。また、再加熱温度は特に限定しないが、生産性を考慮して1000℃から1300℃の範囲とすることが好ましい。熱間圧延は通常の熱延工程、あるいは仕上圧延においてスラブを接合し圧延する連続化熱延工程のどちらでも可能である。熱間圧延の際の圧延終了温度は生産性や板厚精度を考慮してAr3変態点以上とすることが望ましい。熱間圧延後の冷却は通常の方法で行うが、その際の巻取温度は生産性の観点からは550℃以上とすることが好ましく、また、巻取温度が高すぎる場合には酸洗性が劣化するため750℃以下とすることが望ましい。酸洗、冷間圧延は常法でよい。
本発明において、ろ波中心線うねりWcaが0.75μm以下の熱間プレス用鋼板に対して、Ac3変態点~1000℃の温度範囲に加熱した後熱間プレスすることにより、塗装鮮映性に優れた熱間プレス部材を得ることができる。
本発明において、少なくとも一方の面のろ波中心線うねりWcaが0.75μm以下である熱間プレス用めっき鋼板を、Ac3変態点~1000℃の温度範囲に昇温し熱間プレスしたのち、厚さが15μm以上である塗膜層を設けることにより、外観品質に優れた塗装部材を製造することができる。塗装方法は限定されないが、用いる塗料の種類に応じて適当なものを選択することができ、例えばカチオン電着塗装、静電塗装やスプレーによる塗装が例示される。
<溶融めっき法>
冷延鋼板を、溶融めっき設備によって、溶融Al-Si系または溶融Zn-Al系めっき浴中に浸漬し、その後N2ガスワイピングを行って、表1の水準No.1~7およびNo.13~18の熱間プレス用めっき鋼板を作製した。また、冷延鋼板を、溶融めっき設備によって、溶融Znめっき浴中に浸漬し、その後N2ガスワイピングを行って、さらにその後直接通電加熱炉による合金化処理を施すことで、表1の水準No.8~12の熱間プレス用めっき鋼板を作製した。溶融めっきまたは合金化処理後、種々の粗度を有するロールで調質圧延を行うことで、WcaおよびRaを変化させた。
<電気めっき法>
まず、原板を種々の粗度を有するロールで調質圧延を行うことで、WcaおよびRaを変化させた。次いで、硫酸亜鉛・7水和物115g/L、硫酸ニッケル・6水和物230g/L、硫酸ナトリウム55g/Lからなるめっき浴中(pH1.4、浴温50℃)で電流密度を10~100A/dm2、通電時間5~60秒と変化させて電気めっき処理を施すことで、Ni含有率12%のZn-Ni系合金めっき層を形成させ、表1に示す水準No.19~22の熱間プレス用めっき鋼板を作製した。
一部の水準については、引張加工または酸性溶液への浸漬により、めっき鋼板表面にクラックを付与した。引張加工は、熱間プレス用鋼板を圧延方向に伸長率5%で一軸引張加工することで行った。酸性溶液への浸漬は、めっき鋼板を、硫酸亜鉛・7水和物115g/L、硫酸ニッケル・6水和物230g/L、硫酸ナトリウム55g/LからなるpH1.4、浴温50℃の水溶液に40秒間浸漬することで行った。上記のようなクラック付与処理を行った後の熱間プレス用鋼板について、表面観察を行い、クラック密度を測定した。具体的には、熱間プレス用鋼板の表面を、走査型電子顕微鏡(SEM)を用いて1000倍で観察し、任意に3本直線を引き、クラックとの交点を数え、直線の長さで除することにより、単位長さ当たりのクラック密度(箇所/mm)に換算した。このとき、クラック密度の測定精度を上げるため、1つの供試材について3視野の表面観察を行い、その平均値をクラック密度とした。クラック付与方法およびクラックの数密度を表1に示す。
表面の幾何学的形状(ろ波中心線うねりWca、線粗さRa、スキューネスRsk)は、東京精密製サーフコム1500SD3を用い、JIS B0601に従って測定した。表面の幾何学的形状の測定は、熱間プレス部材については、前記中塗り・上塗り塗装を施される面で測定した。両面に中塗り・上塗り塗装を施される場合は両面で測定した。熱間プレス用鋼板については、熱間プレス後に前記中塗り・上塗り塗装を施される面で測定した。両面に中塗り・上塗り塗装を施される場合は両面で測定した。
塗装後鮮映性は、BYK-Gardener社製Wavescan Dual Plusを用い測定し、Wavescan DOIを指標として評価した。0.1~30mmまでの各波長域に対応するWa、Wb、Wc、Wd、Weの値に対し、以下の基準で判定を行い、◎、○、△を合格とし、×を不合格とした。評価結果を表1に示す。
◎(合格、特に優れる):Wa、Wb、Wc、Wd、Weのすべてが15未満かつ最大のものと最小のものの差が5未満
○(合格、より優れる):Wa、Wb、Wc、Wd、Weのすべてが15未満かつ最大のものと最小のものの差が5以上
△(合格):Wa、Wb、Wc、Wd、Weの値のうち、最大値が15以上20未満
×(不合格):Wa、Wb、Wc、Wd、Weの値のうち、最大値が20以上
<塗装後耐食性>
リン酸亜鉛系化成処理および電着塗装と3コート塗装とを施した熱間プレス部材を腐食試験(SAE-J2334)に供し、120サイクル後の腐食状況の評価を行った。クロスカットからの片側最大膨れ幅を測定して以下の基準で判定を行い、◎、○、△を合格とし、×を不合格とした。評価結果を表1に示す。
◎(合格、特に優れる):片側最大膨れ幅<1.5mm
○(合格、より優れる):1.5mm≦片側最大膨れ幅<3.0mm
△(合格):3.0mm≦片側最大膨れ幅<4.0mm
×(不合格):4.0mm≦片側最大膨れ幅
Claims (9)
- 少なくとも一方の面のろ波中心線うねりWcaが1.5μm以下である、熱間プレス部材。
- 前記少なくとも一方の面の線粗さRaが2.0μm以下、スキューネスRskが0以下である、請求項1に記載の熱間プレス部材。
- 前記少なくとも一方の面に、Al、Zn、Feから選択される1種以上を含有し、厚さが10~80μmであるめっき層を有し、ろ波中心線うねりWcaが1.5μm以下である、請求項1または2に記載の熱間プレス部材。
- 請求項1~3のいずれかに記載の熱間プレス部材を基材とし、前記基材の少なくとも一方の面に、厚さが15μm以上である塗膜層を有する、塗装部材。
- 少なくとも一方の面のろ波中心線うねりWcaが0.75μm以下である、熱間プレス用鋼板。
- 前記少なくとも一方の面の線粗さRaが1.0μm以下であり、かつ前記少なくとも一方の面の任意の1mm長さの断面における単位断面長さ当たりのクラック密度が30箇所/mm以上である、請求項5に記載の熱間プレス用鋼板。
- 前記少なくとも一方の面に、Al、Zn、Feから選択される1種以上を含有し、厚さが3~30μmであるめっき層を有する、請求項5または6に記載の熱間プレス用鋼板。
- 少なくとも一方の面のろ波中心線うねりWcaが0.75μm以下である熱間プレス用鋼板を、Ac3変態点~1000℃の温度範囲に加熱後熱間プレスする、熱間プレス部材の製造方法。
- 少なくとも一方の面のろ波中心線うねりWcaが0.75μm以下である熱間プレス用鋼板を、Ac3変態点~1000℃の温度範囲に昇温し熱間プレスしたのち、厚さが15μm以上である塗膜層を設ける、塗装部材の製造方法。
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JP2022506878A JP7063430B1 (ja) | 2021-01-22 | 2021-10-22 | 熱間プレス部材、塗装部材、熱間プレス用鋼板、および熱間プレス部材の製造方法ならびに塗装部材の製造方法 |
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