EP3199257B1 - Method of manufacturing hot press-formed part, and hot press-formed part - Google Patents
Method of manufacturing hot press-formed part, and hot press-formed part Download PDFInfo
- Publication number
- EP3199257B1 EP3199257B1 EP15843885.3A EP15843885A EP3199257B1 EP 3199257 B1 EP3199257 B1 EP 3199257B1 EP 15843885 A EP15843885 A EP 15843885A EP 3199257 B1 EP3199257 B1 EP 3199257B1
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- EP
- European Patent Office
- Prior art keywords
- steel sheet
- cooling
- press
- less
- press forming
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- 238000004519 manufacturing process Methods 0.000 title claims description 18
- 229910000831 Steel Inorganic materials 0.000 claims description 199
- 239000010959 steel Substances 0.000 claims description 199
- 238000001816 cooling Methods 0.000 claims description 173
- 238000007747 plating Methods 0.000 claims description 68
- 238000000034 method Methods 0.000 claims description 41
- 238000010438 heat treatment Methods 0.000 claims description 29
- 229910007567 Zn-Ni Inorganic materials 0.000 claims description 27
- 229910007614 Zn—Ni Inorganic materials 0.000 claims description 27
- 238000010791 quenching Methods 0.000 claims description 16
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- 230000000171 quenching effect Effects 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 229910052750 molybdenum Inorganic materials 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 229910052720 vanadium Inorganic materials 0.000 claims description 5
- 239000012535 impurity Substances 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 238000007731 hot pressing Methods 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910052758 niobium Inorganic materials 0.000 claims 1
- 239000010410 layer Substances 0.000 description 65
- 230000000052 comparative effect Effects 0.000 description 29
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- 239000010960 cold rolled steel Substances 0.000 description 17
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- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 15
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- 229910001338 liquidmetal Inorganic materials 0.000 description 4
- 238000005554 pickling Methods 0.000 description 4
- 239000002344 surface layer Substances 0.000 description 4
- 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 4
- 238000000137 annealing Methods 0.000 description 3
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- 229910052804 chromium Inorganic materials 0.000 description 3
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- 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
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- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
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- 150000002500 ions Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
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Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D—WORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D22/00—Shaping without cutting, by stamping, spinning, or deep-drawing
- B21D22/20—Deep-drawing
- B21D22/208—Deep-drawing by heating the blank or deep-drawing associated with heat treatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D—WORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D22/00—Shaping without cutting, by stamping, spinning, or deep-drawing
- B21D22/20—Deep-drawing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D—WORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D22/00—Shaping without cutting, by stamping, spinning, or deep-drawing
- B21D22/20—Deep-drawing
- B21D22/201—Work-pieces; preparation of the work-pieces, e.g. lubricating, coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D—WORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D24/00—Special deep-drawing arrangements in, or in connection with, presses
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D—WORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D37/00—Tools as parts of machines covered by this subclass
- B21D37/16—Heating or cooling
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- 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
- C21D1/62—Quenching devices
- C21D1/673—Quenching devices for die quenching
-
- 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
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- 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
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/001—Ferrous alloys, e.g. steel alloys containing N
-
- 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
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
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- 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
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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- 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
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
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- 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
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- 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
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- 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
- C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
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- 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
- C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
- C23C2/022—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
- C23C2/0224—Two or more thermal pretreatments
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- 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
- C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
- C23C2/024—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by cleaning or etching
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- 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
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/26—After-treatment
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- 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
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
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- 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
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F17/00—Multi-step processes for surface treatment of metallic material involving at least one process provided for in class C23 and at least one process covered by subclass C21D or C22F or class C25
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D3/00—Electroplating: Baths therefor
- C25D3/02—Electroplating: Baths therefor from solutions
- C25D3/56—Electroplating: Baths therefor from solutions of alloys
- C25D3/565—Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of zinc
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/48—After-treatment of electroplated surfaces
Definitions
- the present invention relates to a method of manufacturing a hot press-formed part according to claim 1 and particularly, to a method of manufacturing a hot press-formed part from a coated steel sheet that enables press forming of the coated steel sheet which is heated beforehand, whereby the coated steel sheet can be quenched to attain a predetermined strength (tensile strength: 1180 MPa or higher) while being formed into a predetermined shape.
- a predetermined strength tensile strength: 1180 MPa or higher
- some conventional techniques propose performing hot press forming of a blank sheet heated to high temperature to have a desired shape using a tool of press forming, while quenching the blank sheet in the tool of press forming by utilizing heat extraction, to achieve high-strengthening of the hot press-formed part.
- GB1490535A proposes a technique in which, when manufacturing a part of a predetermined shape by hot press forming a blank sheet (steel sheet) heated to an austenite single phase region at around 900 °C, the blank sheet is quenched in a tool of press forming simultaneously with the hot press forming, thus providing high-strengthening of the part.
- the technique proposed in PTL 1 has a problem in that if the steel sheet is heated to a temperature as high as around 900 °C before subjection to the press forming, oxided scale (ion oxide) forms on the surface of the steel sheet, and the oxided scale peels during the hot press forming and damages the tool of press forming or the surface of the press formed part. Besides, the oxided scale remaining on the surface of the part causes poor appearance and degraded coating adhesion properties. Accordingly, the oxided scale on the surface of the part is typically removed by a process such as pickling or shot blasting. Such a process, however, causes lower productivity.
- JP3663145B proposes a technique in which a steel sheet coated with Zn or a zinc-based alloy is heated to 700 °C to 1200 °C and then hot press formed to obtain a hot press-formed part having a Zn-Fe-based compound or a Zn-Fe-Al-based compound on its surface.
- PTL 2 describes that the use of the steel sheet coated with Zn or a zinc-based alloy can suppress the oxidation of the surface of the steel sheet during heating before hot press forming, and provide a hot press-formed part having excellent corrosion resistance.
- the generation of oxided scale on the surface of the hot press-formed part is suppressed to some extent.
- Zn in the plating layer may induce liquid metal embrittlement cracking, causing cracks of about 100 ⁇ m in depth in the surface layer part of the hot press-formed part.
- Such cracks pose various problems, such as a decrease in the fatigue resistance of the hot press-formed part.
- JP201391099A proposes a method that includes heating a coated steel sheet having a Zn-Fe-based plating layer formed on the steel sheet surface to a temperature from the Ac 1 transformation temperature of the steel sheet to 950 °C, and cooling the coated steel sheet to a temperature at or below the freezing point of the plating layer before starting press forming.
- PTL 3 describes that liquid metal embrittlement cracking can be suppressed by starting the press forming after the coated steel sheet is cooled to a temperature at or below the freezing point of the plating layer.
- PTL 4 relates to a method for producing a hardened steel component with regions of different hardness and/or ductility; a blank is stamped out and either heated in some regions to a temperature ⁇ Ac3, and then transferred to a forming die, is formed, and is cooled at a speed that is greater than the critical hardening speed and thus hardened or is cold formed into the finished shape and the formed blank is heated in some regions to a temperature >Ac3 and then transferred to a hardening die and is hardened at a speed greater than the critical hardening speed; the steel material is adjusted in a transformation-delaying fashion so that a quench hardening through transformation of austenite into martensite takes place at a forming temperature that lies in the range from 450° C to 700° C; after the heating and before the forming, an active cooling takes place at >15 K/s.
- the technique proposed in PTL 3 can suppress liquid metal embrittlement cracking, i.e., cracks in the surface of the hot press-formed part, which are about 100 ⁇ m in depth from the interface between the plating layer and the steel sheet (steel) toward the inside of the steel sheet, and in which Zn is detected at its interface (such cracks referred to hereinafter as "macro-cracks").
- macro-cracks we studied the use of Zn-Ni alloy coating obtained by blending Zn with about 9 % to 25 % of Ni as a plating layer with high melting point. To ensure the corrosion resistance of a Zn-Ni alloy, the Zn-Ni alloy needs to be ⁇ -phase.
- the ⁇ -phase in the phase equilibrium diagram of Zn-Ni alloy has a melting point of 860 °C or higher, which is very high as compared to that of a normal Zn or Zn alloy plating layer, making it possible to suppress macro-cracks under normal press conditions.
- microfissures which are about 30 ⁇ m or less in depth from the interface between the plating layer and the steel sheet toward the inside of the steel sheet, and in which Zn is not detected at its interface, may also occur in the surface of the hot press formed-part.
- micro-cracks Such microfissures are called "micro-cracks", which pass through the interface between the plating layer and the steel sheet and reach the inside of the steel sheet, adversely affecting the characteristics (fatigue resistance, etc.) of the hot press-formed part. Macro-cracks also occur in, for example, a round portion of the die shoulder on the punch-contacting side which is subjected to only tensile strain while press forming of a hat-shaped section part. On the other hand, micro-cracks do not occur in such area, but on the die-contacting side of wall portions, which are subjected to compression (due to bending) followed by tensile strain (due to bend restoration). It is thus estimated that macro-cracks and micro-cracks are produced by different mechanisms.
- PTL 3 may suppress the occurrence of macro-cracks in a coated steel sheet having a Zn-Fe-based plating layer formed thereon, but is not necessarily effective for suppressing the occurrence of micro-cracks, because it does not consider potential micro-cracks occurring in a coated steel sheet having a Zn-Ni plating layer formed thereon.
- the coated steel sheet is press formed in a state where the entire coated steel sheet has been cooled to a temperature at or below the freezing point of the plating layer, without specifying the lowest temperature at which the press forming can be started.
- micro-cracks microfissures
- press forming of a steel sheet coated with Zn or a zinc-based alloy at high temperature at or below the freezing point of the plating layer may cause microfissures in the surface of the steel sheet.
- Similar microfissures also occur in a Zn-Ni coated steel sheet during press forming.
- Such microfissures are about 30 ⁇ m in depth from the interface between the plating layer and the steel sheet, and pass through the interface between the plating layer and the steel sheet and reach the inside of the steel sheet.
- micro-cracks are not caused by compressive deformation or bending deformation alone, but are caused at those portions that are subjected to deformation resulting from bending and subsequent bend restoration.
- forming as described above may limited to a particular range, but in some cases the portions of the steel sheet subjected to forming that would cause micro-cracks may be extensive depending on the shape of the formed part.
- the temperature of the steel sheet would become lower at the time of press forming and shape accuracy would degrade.
- the steel sheet was cooled to a temperature of 550 °C or lower and 410 °C or higher at a cooling rate of 100 °C/s or higher, and when press forming of the steel sheet was started within 5 seconds after the cooling while the temperature of the steel sheet was 550 °C or lower and 400 °C or higher, there was almost no loss of shape accuracy.
- the steel sheet when the heated steel sheet is quenched with the press tool for cooling and subjected to press forming while the steel sheet temperature is 550 °C or lower and 400 °C or higher, the steel sheet has a microstructure of austenite during the press forming, and austenite transforms to martensite after the press forming, thereby relieving the stress accumulating during the press forming.
- the present invention provides a method of manufacturing a hot press-formed part according to claims 1 and 2 as well as a hot press-formed part manufactured by said method.
- the present invention it becomes possible to provide hot press-formed parts, using coated steel sheets as steel sheets, that are free from micro-cracks throughout both front and back surfaces and that have sufficient hardness and satisfactory shape fixability without a significant increase in press forming load, and thus to manufacture automotive parts and the like in a variety of product shapes using coated steel sheets with high strength.
- a method of manufacturing a hot press-formed part by hot pressing a coated steel sheet 1 formed with a Zn-Ni plating layer on a surface of a steel sheet as illustrated in FIG. 1 comprises: heating (not shown) the coated steel sheet 1 to a temperature range of Ac 3 transformation temperature to 1000 °C; cooling (S1) the heated coated steel sheet I to a temperature of 550 °C or lower and 410 °C or higher, at a cooling rate of 100 °C/s or higher, by squeezing the coated steel sheet 1 with a press tool for cooling 3 having flat surfaces configured to contact the coated steel sheet 1; starting (S2) press forming of the coated steel sheet 1 with a tool of press forming 11 within 5 seconds after the cooling while the temperature of the coated steel sheet 1 is 550 °C or lower and 400 °C or higher, to obtain a formed body 1'; and quenching (S3) the formed body 1', while squeezing the formed body with the tool of press forming 11 and
- a coated steel sheet formed with a Zn-Ni plating layer on a surface of a steel sheet is used as the material of a hot press-formed part.
- the provision of a Zn-Ni plating layer on a surface of the steel sheet ensures the corrosion resistance of the part after subjection to hot press forming.
- the method of forming a Zn-Ni plating layer on a surface of the steel sheet is not particularly limited, and any methods such as hot-dip galvanizing and electrogalvanizing may be used.
- the coating weight per side is preferably 10 g/m 2 or more and 90 g/m 2 or less.
- the Ni content in the plating layer is preferably 9 mass% or more and 25 mass% or less.
- a ⁇ phase having any of the crystal structures of Ni 2 Zn 11 , NiZn 3 , or Ni 5 Zn 21 is formed when the Ni content in the plating layer is 9 mass% or more and 25 mass% or less.
- the ⁇ phase has a high melting point, and thus is advantageous in preventing the plating layer from evaporating when heating the coated steel sheet before subjection to hot press forming.
- the ⁇ phase is also advantageous in suppressing liquid metal embrittlement cracking during high-temperature hot press forming.
- the coated steel sheet 1 is heated to a temperature range of Ac 3 transformation temperature to 1000 °C. If the heating temperature of the coated steel sheet I is below Ac 3 transformation temperature, a sufficient amount of austenite cannot be obtained during heating, leading to the presence of ferrite during press forming. As a result, it becomes difficult to obtain sufficient strength or good shape fixability through hot press forming.
- the heating temperature of the coated steel sheet 1 exceeds 1000 °C, on the other hand, the plating layer evaporates or excessive oxide generation occurs in the surface layer part, as a result of which the oxidation resistance or the corrosion resistance of the hot press-formed part decreases. Therefore, the heating temperature is from Ac 3 transformation temperature to 1000 °C.
- the heating temperature is from Ac 3 transformation temperature + 30 °C to 950 °C.
- the method of heating the coated steel sheet 1 is not particularly limited, and any methods may be used, such as heating in an electric furnace, induction heating furnace, or direct current furnace.
- the coated steel sheet 1 thus heated is cooled to a temperature of 550 °C or lower and 410 °C or higher at a cooling rate of 100 °C/s or higher, by being squeezed with the press tool for cooling 3.
- the press tool for cooling 3 comprises an upper cooling tool 5 and a lower cooling tool 7, each having a flat surface configured to contact the coated steel sheet 1.
- An extendable lifter pin 9 is provided on the lower cooling tool 7. The heated coated steel sheet 1 is placed on the lifter pin 9, and cooled by being squeezed between the upper cooling tool 5 and the lower cooling tool 7.
- both front and back surfaces of the coated steel sheet 1 may be squeezed entirely with the press tool for cooling 3 as illustrated in FIG. 1 .
- the coated steel sheet 1 may be placed with some portions, such as portions to be trimmed afterwards before finishing operations to form a final product, extending beyond the edges of the press tool for cooling 3.
- portions subjected to forming that would cause micro-cracks, i.e., bending-bend restoration deformation cover a large area of the coated steel sheet 1 as the working material, it is possible to suppress the occurrence of micro-cracks throughout both front and back surfaces of the resulting press formed part.
- the temperature at start of squeezing the heated coated steel sheet I with the press tool for cooling 3 is preferably 800 °C or lower from the perspective of preventing the risk of the Zn-Ni plating layer being adhered to the press tool for cooling, and preferably 670 °C or higher from the perspective of guaranteeing the strength after hot press forming.
- the coated steel sheet 1 may be cooled with one surface pressed against the press tool for cooling 3.
- the cooling rate is set to be 100 °C/s or higher because this cooling rate enables the press formed part to have a martensite single phase structure, and thus allows for strengthening, without increasing cost. In the following, this will be described in detail.
- FIG, 2 schematically illustrates the relationship between a typical metallographic structure, temperature, and cooling time when a steel sheet is subjected to hot press forming using a tool of press forming.
- FIG. 2A shows a case where the press forming start temperature is high and, after the start of press forming, the coated steel sheet is rapidly cooled by heat extraction to the tool of press forming, so as to have a martensite single phase structure.
- a martensite single phase structure can be obtained while lowing the forming start temperature, as indicated by a dashed curve in FIG. 3 .
- the upper limit of the cooling rate is normally around 500 °C/s.
- the cooling stop temperature is set to be 550 °C or lower because, above 550 °C, cooling becomes insufficient, causing micro-cracks after the hot press forming.
- the cooling stop temperature is preferably 500 °C or lower.
- the lower limit of the cooling stop temperature is 410 °C because, below 410 °C, the coated steel sheet 1 is excessively cooled before subjection to the press forming, leading to deterioration in shape fixability after subjection to the press forming.
- the cooling stop temperature is preferably 430 °C or higher.
- the cooling rate and the cooling stop temperature may be controlled by, for example, varying the time to hold the coated steel sheet 1 with the press tool for cooling 3 (see FIG. 1 ).
- Changes in the temperature of the coated steel sheet 1 when squeezed with the press tool for cooling 3 may be determined by measuring the temperature of the coated steel sheet 1 using a sheath type thermocouple 19 of 0.5 mm ⁇ inserted into the steel sheet in a manner as illustrated in FIG. 4 .
- FIG. 5 is a graph showing some of the results, where the vertical axis is temperature (°C) and the horizontal axis is time (s).
- FIG. 6 is a graph representing a partial enlarged view of FIG.
- press formed parts were formed at different conditions by varying the holding time during which the press formed part was being held in the press tool for cooling (in particular, the cooling stop temperature set for the press tool for cooling), and the press forming start temperature, which will be described below, and evaluation was made of the following parameters.
- FIG. 7 shows SEM (Scanning Electron Microscope) images of cross sections of surface layers, on the side contacting a die 13, of wall portions of press formed parts that were formed at different conditions by varying the time to cool the press formed part in the press tool for cooling (the cooling stop temperature set for the press tool for cooling) and the press forming start temperature. It can be seen from FIGS. 7A-7C that no micro-cracks were observed in the steel sheets with a cooling time in the press tool for cooling of 0.9 s or more (and a press forming start temperature of 550 °C or lower). Under all conditions, Hv > 450, proving that quench hardenability does not deteriorate.
- FIG. 8 shows the relationship between press forming start temperature and press forming load, where the vertical axis is the press forming load (kN) and the horizontal axis is the press forming start temperature (°C). It can be seen from FIG. 8 that a reduction in the press forming start temperature caused by the process of cooling in the press tool for cooling prior to press forming caused an increased press forming load, which was, however, equivalent to that on mild steel (270D, cold deep forming) at temperatures around 550 °C at which micro-cracks do not occur, and thus posed no problem.
- mild steel 270D, cold deep forming
- FIG. 9 shows the relationship between press forming start temperature and amount of mouth opening deformation, where the vertical axis is the amount of mouth opening deformation (mm) of a formed part and the horizontal axis is the press forming start temperature (°C).
- the amount of mouth opening deformation increases due to a decrease in the forming start temperature caused by the process of cooling in the press tool for cooling prior to the press forming process, which shows a tendency such that shape fixability deteriorates accordingly.
- the press forming start temperature is 400 °C or higher, almost no deterioration of shape fixability is observed.
- the coated steel sheet 1 is press formed into the shape of a product.
- the press forming is performed with the tool of press forming 11 after the cooling.
- the tool of press forming 11 comprises a die 13 and a punch 17 as illustrated in FIG. 1 .
- the coated steel sheet 1 is press formed by being squeezed between the die 13 and the punch 17, to obtain a formed body 1'.
- the press forming is started within 5 seconds after the cooling because, if press forming is started after expiry of the time limit of 5 seconds after the cooling, for example, ferrite and bainite are formed before the start of press forming, preventing formation of a martensite single phase structure. As a result, the press formed part has insufficient hardness. Press forming is preferably started within 3 seconds after the cooling. No lower limit is particularly placed on the time limit, yet a preferred time limit is normally 1 second or more.
- the present disclosure is not limited to a particular press forming method.
- available methods include, for example, draw forming whereby the coated steel sheet 1 is subjected to forming while being squeezed between the die 13 and the blank holder 15 as illustrated in FIG. 10A , and crash forming whereby the coated steel sheet 1 is subjected to forming while lowering the blank holder 15, or alternatively, without using the blank holder 15, as illustrated in FIG. 10B .
- crash forming is preferred because of less excessive forming of wall portions of the press formed part.
- the formed body 1' is quenched while being squeezed and held in the tool of press forming 11, to obtain a hot press-formed part.
- the press slide of the formed body 1' is stopped at its press bottom dead center after subjection to the press forming.
- the sliding stop time is preferably 3 seconds or more, although it varies with the amount of heat released by the tool of press forming. No upper limit is particularly placed on the sliding stop time, yet it is preferably 20 seconds or less from the perspective of productivity.
- a hot-rolled or cold-rolled steel sheet having a chemical composition containing (consisting of), for example, in mass%, C: 0.15 % or more and 0.50 % or less, Si: 0.05 % or more and 2.00 % or less, Mn: 0.50 % or more and 3.00 % or less, P: 0.10 % or less, S: 0.050 % or less, Al: 0.10 % or less, and N: 0.010 % or less, and the balance consisting of Fe and unavoidable impurities.
- the following provides a description of the chemical composition. When the composition is expressed in "%”, this refers to "mass%" unless otherwise specified.
- the C content is an element that improves the strength of steel.
- the C content is preferably 0.15 % or more.
- the C content exceeds 0.50 %, on the other hand, the weldability of the hot press-formed part and the fine blanking workability of the material (steel sheet) decrease significantly. Accordingly, the C content is preferably 0.15 % or more and 0.50 % or less, and more preferably 0.20 % or more and 0.40 % or less.
- the Si is an element that improves the strength of steel, as with C.
- the Si content is preferably 0.05 % or more.
- the Si content exceeds 2.00 %, on the other hand, a surface defect, called red scale, increases significantly during hot rolling for manufacturing a steel sheet. Accordingly, the Si content is preferably 0.05 % or more and 2.00 % or less, and more preferably 0.10 % or more and 1.50 % or less.
- Mn is an element that enhances the quench hardenability of steel, and is effective in suppressing the ferrite transformation of the steel sheet and improving quench hardenability in the cooling process after the hot press forming. Mn also has a function of lowering the Ac 3 transformation temperature, and thus is an element effective in lowering the heating temperature of the coated steel sheet 1 before subjection to hot press forming. To achieve these effects, the Mn content is preferably 0.50 % or more. When the Mn content exceeds 3.00 %, on the other hand, Mn segregation occurs, reducing the uniformity of characteristics of the steel sheet and of the hot press-formed part. Accordingly, the Mn content is preferably 0.50 % or more and 3.00 % or less, and more preferably 0.75 % or more and 2.50 % or less.
- the P content exceeds 0.10 %, P segregates to grain boundaries, reducing the low-temperature toughness of the steel sheet and of the hot press-formed part. Accordingly, the P content is preferably 0.10 % or less, and more preferably 0.01 % or less. Excessively reducing the P content, however, leads to increased cost in the steelmaking process. Therefore, the P content is preferably 0.003 % or more.
- S is an element that forms a coarse sulfide by combining with Mn and causes a decrease in ductility of steel.
- the S content is preferably reduced as much as possible, though up to 0.050 % is allowable. Accordingly, the S content is preferably 0.050 % or less, and more preferably 0,010 % or less. Excessively reducing the S content, however, leads to increased cost of desulfurization in the steelmaking process. Therefore, the S content is preferably 0.0005 % or more.
- the Al content exceeds 0.10 %, oxide inclusions in steel increase, and the ductility of steel decreases. Accordingly, the Al content is preferably 0.10 % or less, and more preferably 0.07 % or less. Al functions as a deoxidation material, however, and from the perspective of improving the cleanliness factor of steel, the Al content is preferably 0.01 % or more.
- the N content exceeds 0.010 %, nitrides such as AIN form in the steel sheet, which causes lower formability during hot press forming. Accordingly, the N content is preferably 0.010 % or less, and more preferably 0.005 % or less. Excessively reducing the N content, however, leads to increased cost in the steelmaking process. Therefore, the N content is preferably 0.001 % or more.
- the steel sheet may further contain one or more of the following elements as necessary:
- Cr, V, Mo, and Ni are each an element effective in enhancing the quench hardenability of steel. This effect is achieved when the content of any of these elements contained is 0.01 % or more. However, adding any of Cr, V, Mo, or Ni beyond 0.50 % fails to further increase this effect, but instead increases cost. Accordingly, in the case where one or more of Cr, V, Mo, and Ni is included, the content is preferably 0.01 % or more and 0.50 % or less, and more preferably 0,10 % or more and 0.40 % or less.
- Ti is effective for strengthening steel.
- the strengthening effect of Ti is achieved when the content is 0.01 % or more.
- Ti can be used to strengthen steel without any problem as long as the content is within the range specified herein.
- adding Ti beyond 0.20 % fails to increase this effect, but instead increases cost.
- the content is preferably 0.01 % or more and 0.20 % or less, and more preferably 0.01 % or more and 0.05 % or less.
- Nb 0.01 % or more and 0.10 % or less
- Nb is also effective for strengthening steel.
- the strengthening effect of Nb is achieved when the content is 0.01 % or more.
- Nb can be used to strengthen steel without any problem as long as the content is within the range specified herein.
- adding Nb beyond 0.10 % fails to increase this effect, but instead increases cost.
- the content is preferably 0.01 % or more and 0.10 % or less, and more preferably 0.01 % or more and 0.05 % or less.
- B is an element that enhances the quench hardenability of steel, and is effective in suppressing the generation of ferrite from austenite grain boundaries and obtaining a quenched microstructure when cooling the steel sheet after subjection to the hot press forming.
- This effect is achieved when the B content is 0.0002 % or more.
- adding B beyond 0.0050 % fails to increase this effect, but instead increases cost.
- the content is preferably 0.0002 % or more and 0.0050 % or less, and more preferably 0.0005 % or more and 0.0030 % or less.
- the Sb has the effect of suppressing generation of a decarburized layer in the surface layer part of the steel sheet during the period from when a steel sheet is heated before subjection to hot press forming to when the steel sheet is cooled through a series of hot press forming processes.
- the Sb content is preferably 0.003 % or more.
- the content is preferably 0.003 % or more and 0.030 % or less, and more preferably 0.005 % or more and 0.010 % or less.
- the components (balance) other than the above are Fe and unavoidable impurities.
- the manufacturing conditions of the coated steel sheet 1 used as the material of the hot press-formed part are not particularly limited.
- the steel sheet may be a hot-rolled steel sheet (pickled steel sheet) having a predetermined chemical composition or a cold-rolled steel sheet obtained by subjecting the hot-rolled steel sheet to cold rolling.
- the formation of a Zn-Ni plating layer on a surface of the steel sheet for obtaining the coated steel sheet 1 is not limited to particular conditions.
- the coated steel sheet 1 may be obtained by subjecting the hot-rolled steel sheet (pickled steel sheet) to Zn-Ni coating treatment.
- the coated steel sheet 1 may be obtained by subjecting the cold-rolled steel sheet to Zn-Ni coating treatment either directly after subjection to the cold rolling, or after subjection to annealing treatment following the cold rolling.
- the Zn-Ni plating layer may be formed by degreasing and pickling the steel sheet, and then subjecting the steel sheet to electrogalvanizing treatment with a current density of 10 A/dm 2 or more and 150 A/dm 2 or less, in a plating bath which has a pH of 1.0 or more and 3.0 or less and a bath temperature of 30 °C or higher and 70 °C or lower, and which contains 100 g/L or more and 400 g/L or less nickel sulfate hexahydrate and 10 g/L or more and 400 g/L or less zinc sulfate heptahydrate.
- the cold-rolled steel sheet may be subjected to annealing treatment before subjection to the degreasing and pickling.
- the Ni content in the plating layer may be set within the desired range (for example, 9 mass% to 25 mass%) by appropriately adjusting the concentration of zinc sulfate heptahydrate or the current density within the above-mentioned range.
- the coating weight of the Zn-Ni plating layer may be set within the desired range (for example, 10 g/m 2 to 90 g/m 2 per side) by adjusting the energizing time.
- the hot-rolled steel sheet was then pickled and cold rolled with a reduction of 50 %, to obtain a cold-rolled steel sheet with a thickness of 1.6 mm.
- the Ac 3 transformation temperature in Table 1 was calculated by Formula (1) below (see William C. Leslie, "The Physical Metallurgy of Steels", translation supervised by Nariyasu Kouda, translated by Hiroshi Kumai and Tatsuhiko Noda, Maruzen Co., Ltd., 1985, p. 273 ).
- a cold-rolled steel sheet was passed through a continuous hot-dip galvanizing line, heated to a temperature range of 800 °C to 900 °C at a heating rate of 10 °C/s, and held in this temperature range for 10 s or more and 120 s or less. Subsequently, the cold-rolled steel sheet was cooled to a temperature range of 460 °C to 500 °C at a cooling rate of 15 °C/s, and dipped into a galvanizing bath at 450 °C to form a Zn plating layer. The coating weight of the Zn plating layer was adjusted to a predetermined coating weight using a gas wiping method.
- a cold-rolled steel sheet was passed through a continuous hot-dip galvanizing line, heated to a temperature range of 800 °C to 900 °C at a heating rate of 10 °C/s, and held in this temperature range for 10 s or more and 120 s or less. Subsequently, the cold-rolled steel sheet was cooled to a temperature range of 460 °C to 500 °C at a cooling rate of 15 °C/s, and dipped into a galvanizing bath at 450 °C to form a Zn plating layer. The coating weight of the Zn plating layer was adjusted to a predetermined coating weight using a gas wiping method.
- the cold rolled steel sheet was heated to a temperature range of 500 °C to 550 °C and held for 5 s to 60 s in an alloying furnace, thereby forming a Zn-Fe plating layer.
- the Fe content in the plating layer was set to a predetermined content by changing the heating temperature in the alloying furnace and the holding time at the heating temperature within the above-mentioned ranges.
- the cold-rolled steel sheet was passed through a continuous annealing line, heated to a temperature range of 800 °C to 900 °C at a heating rate of 10 °C/s, and held in this temperature range for 10 s or more and 120 s or less. Subsequently, the cold-rolled steel sheet was cooled to a temperature range of 500 °C or lower at a cooling rate of 15 °C/s.
- the cold-rolled steel sheet was subjected to degreasing and pickling, followed by electrogalvanizing treatment whereby the cold-rolled steel sheet was energized for 10 s to 100 s with a current density of 30 A/dm 2 to 100 A/dm 2 , in a plating bath containing 200 g/L nickel sulfate hexahydrate and 10 g/L to 300 g/L zinc sulfate heptahydrate and having a pH of 1.3 and a bath temperature 50 °C, thereby forming a Zn-Ni plating layer.
- the Ni content in the plating layer was set to a predetermined content by appropriately adjusting the concentration of zinc sulfate heptahydrate and the current density within the above-mentioned ranges.
- the coating weight of the Zn-Ni plating layer was set to a predetermined coating weight by appropriately adjusting the energizing time within the above-mentioned range.
- a blank sheet of 200 mm ⁇ 400 mm was blanked from each coated steel sheet thus obtained, and heated in an electric furnace in air atmosphere.
- the blank sheet was then placed and cooled in a press tool for cooling (material: SKD61), and subjected to press forming and quenching using a tool of press forming under the conditions presented in Table 2.
- the blank sheet was released from the tool of press forming to manufacture a press formed part with a hat-shaped section as illustrated in FIG. 11 .
- the round portion of punch shoulder was 6 mm and the round portion of die shoulder was 6 mm.
- the press forming was performed with a punch-die clearance of 1.6 mm. Cooling prior to press forming was performed by bringing the blank sheet into contact with the press tool for cooling. Press forming was performed either by draw forming under a blank holder force of 98 kN, or crash forming without using a blank holder.
- Table 2 shows the blank sheet heating temperature, type of steel sheet, type of plating layer, heating conditions, cooling conditions, and press forming conditions.
- micro-crack depth refers to, as illustrated in FIG.
- each press formed part was evaluated based on the amount of mouth opening deformation, which was determined by the difference (W - W 0 ) between the width (W) of each press formed part with a hat-shaped section after die release and the width (W 0 ) of the corresponding formed part when conformed to the shape of the tool of press forming illustrated in FIG. 13 .
- a sample for hardness measurement was collected from a wall portion of each press formed part with a hat-shaped section.
- the hardness of the cross section of each sample was measured using a micro-Vickers hardness meter.
- a test was conducted with a test load of 9.8 N, and hardness measurement was made at five central positions in the thickness direction for each sample, and the average was used as the hardness of the sample. In this case, the targeted hardness was 400 Hv or more.
- a JIS No. 13 B tensile test piece was collected from a wall portion of each press formed part with a hat-shaped section.
- the type of plating layer Zn-Ni plating layer
- cooling process cooling in the press tool for cooling
- cooling time 0.6 s to 1.7 s
- cooling rate (appropriate range: 100 °C/s or higher)
- cooling stop temperature (appropriate range: 410 °C to 550 °C)
- time limit to start press forming after cooling (appropriate range: within 5 seconds)
- press forming start temperature (appropriate range: 400 °C to 550 °C) are all within the appropriate ranges specified in this disclosure.
- the pressed samples according to our examples were free from micro-cracks, and the amount of mouth opening deformation was determined to be 0 mm for these samples. From these results, it can be seen that, with the press forming process disclosed herein, it is possible to suppress the occurrence of micro-cracks while ensuring good shape fixability.
- Comparative Example 1 was subjected to a forming process without being cooled with the press tool for cooling.
- Comparative Examples 2 to 4 were outside the appropriate range (410 °C to 550 °C) in terms of cooling stop temperature. Specifically, the cooling stop temperature was 600 °C in Comparative Example 2, 340 °C in Comparative Example 3, and 290 °C in Comparative Example 4.
- the cooling process was gas cooling, in which the cooling rate was outside the appropriate range (100 °C/s or higher), and thus rapid cooling could not be performed. Accordingly, in Comparative Examples 5 and 6, the cooling stop temperature and the press forming start temperature of the steel sheets were outside the appropriate ranges (cooling stop temperature: 410 °C to 550 °C, press forming start temperature: 400 °C to 550 °C), and micro-cracks occurred. Further, in Comparative Example 7, the cooling stop temperature was 510 °C, which is within the appropriate range. However, the amount of mouth opening deformation was 3 mm, which shows a reduction in the shape fixability.
- Comparative Examples 8 and 9 press forming was started in 10 seconds and 8 seconds respectively after the cooling, exceeding the appropriate time limit of 5 seconds. Accordingly, in Comparative Examples 8 and 9, the amount of mouth opening deformation was 2 mm, and the steel sheets showed a reduction in the hardness and tensile strength after subjection to the press forming.
- Comparative Examples 10 and 11 were different from the examples and other comparative examples in the type of plating layer. Specifically, Comparative Example 10 used a pure Zn plating layer and Comparative Example 11 used a Zn-Fe plating layer. The press forming start temperature at which micro-cracks will not occur in the pure Zn plating layer or in the Zn-Fe plating layer is even lower than the press forming start temperature at which micro-cracks will not occur in a Zn-Ni plating layer. Thus, micro-cracks occurred in Comparative Examples 10 and 11.
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Description
- The present invention relates to a method of manufacturing a hot press-formed part according to
claim 1 and particularly, to a method of manufacturing a hot press-formed part from a coated steel sheet that enables press forming of the coated steel sheet which is heated beforehand, whereby the coated steel sheet can be quenched to attain a predetermined strength (tensile strength: 1180 MPa or higher) while being formed into a predetermined shape. - In recent years, strengthening and sheet metal thinning of automotive parts have been required. As the steel sheets used have higher strength, press formability decreases, and it becomes more difficult to form the steel sheets into the desired part shape.
To solve this problem, some conventional techniques propose performing hot press forming of a blank sheet heated to high temperature to have a desired shape using a tool of press forming, while quenching the blank sheet in the tool of press forming by utilizing heat extraction, to achieve high-strengthening of the hot press-formed part.
For example,GB1490535A - However, the technique proposed in
PTL 1 has a problem in that if the steel sheet is heated to a temperature as high as around 900 °C before subjection to the press forming, oxided scale (ion oxide) forms on the surface of the steel sheet, and the oxided scale peels during the hot press forming and damages the tool of press forming or the surface of the press formed part. Besides, the oxided scale remaining on the surface of the part causes poor appearance and degraded coating adhesion properties. Accordingly, the oxided scale on the surface of the part is typically removed by a process such as pickling or shot blasting. Such a process, however, causes lower productivity. Moreover, although suspension parts of vehicles, structural parts of automotive bodies, and the like are also required to have excellent corrosion resistance, a rust preventive film such as a plating layer is not provided on the blank sheet with the technique proposed inPTL 1. Accordingly, this technique does not provide sufficient corrosion resistance to the hot press-formed part. - For these reasons, there is demand for a hot press forming technique that can suppress the generation of oxided scale during heating before hot press forming, and improve the corrosion resistance of the hot press-formed part. To meet this demand, other conventional techniques propose coated steel sheets having films such as plating layers on their surfaces, hot press forming methods using coated steel sheets, and the like.
For example,JP3663145B PTL 2 describes that the use of the steel sheet coated with Zn or a zinc-based alloy can suppress the oxidation of the surface of the steel sheet during heating before hot press forming, and provide a hot press-formed part having excellent corrosion resistance. - With the technique proposed in
PTL 2, the generation of oxided scale on the surface of the hot press-formed part is suppressed to some extent. However, Zn in the plating layer may induce liquid metal embrittlement cracking, causing cracks of about 100 µm in depth in the surface layer part of the hot press-formed part. Such cracks pose various problems, such as a decrease in the fatigue resistance of the hot press-formed part. - To address these issues,
JP201391099A PTL 3 describes that liquid metal embrittlement cracking can be suppressed by starting the press forming after the coated steel sheet is cooled to a temperature at or below the freezing point of the plating layer. - PTL 4 relates to a method for producing a hardened steel component with regions of different hardness and/or ductility; a blank is stamped out and either heated in some regions to a temperature ≥Ac3, and then transferred to a forming die, is formed, and is cooled at a speed that is greater than the critical hardening speed and thus hardened or is cold formed into the finished shape and the formed blank is heated in some regions to a temperature >Ac3 and then transferred to a hardening die and is hardened at a speed greater than the critical hardening speed; the steel material is adjusted in a transformation-delaying fashion so that a quench hardening through transformation of austenite into martensite takes place at a forming temperature that lies in the range from 450° C to 700° C; after the heating and before the forming, an active cooling takes place at >15 K/s.
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- PTL 1:
GB1490535A - PTL 2:
JP3663145B - PTL 3:
JP201391099A - PTL 4:
US 2014/0027026 A1 - It is believed that the technique proposed in
PTL 3 can suppress liquid metal embrittlement cracking, i.e., cracks in the surface of the hot press-formed part, which are about 100 µm in depth from the interface between the plating layer and the steel sheet (steel) toward the inside of the steel sheet, and in which Zn is detected at its interface (such cracks referred to hereinafter as "macro-cracks").
For suppressing macro-cracks, we studied the use of Zn-Ni alloy coating obtained by blending Zn with about 9 % to 25 % of Ni as a plating layer with high melting point. To ensure the corrosion resistance of a Zn-Ni alloy, the Zn-Ni alloy needs to be γ-phase. The γ-phase in the phase equilibrium diagram of Zn-Ni alloy has a melting point of 860 °C or higher, which is very high as compared to that of a normal Zn or Zn alloy plating layer, making it possible to suppress macro-cracks under normal press conditions.
However, in addition to the macro-cracks, microfissures which are about 30 µm or less in depth from the interface between the plating layer and the steel sheet toward the inside of the steel sheet, and in which Zn is not detected at its interface, may also occur in the surface of the hot press formed-part. Such microfissures are called "micro-cracks", which pass through the interface between the plating layer and the steel sheet and reach the inside of the steel sheet, adversely affecting the characteristics (fatigue resistance, etc.) of the hot press-formed part.
Macro-cracks also occur in, for example, a round portion of the die shoulder on the punch-contacting side which is subjected to only tensile strain while press forming of a hat-shaped section part. On the other hand, micro-cracks do not occur in such area, but on the die-contacting side of wall portions, which are subjected to compression (due to bending) followed by tensile strain (due to bend restoration). It is thus estimated that macro-cracks and micro-cracks are produced by different mechanisms. - In this regard,
PTL 3 may suppress the occurrence of macro-cracks in a coated steel sheet having a Zn-Fe-based plating layer formed thereon, but is not necessarily effective for suppressing the occurrence of micro-cracks, because it does not consider potential micro-cracks occurring in a coated steel sheet having a Zn-Ni plating layer formed thereon.
With the technique proposed inPTL 3, the coated steel sheet is press formed in a state where the entire coated steel sheet has been cooled to a temperature at or below the freezing point of the plating layer, without specifying the lowest temperature at which the press forming can be started. This leads to the problem of a lower press forming temperature resulting in an increase in the strength of the steel sheet during press forming, deteriorating the shape fixability (which is a characteristic that maintains the shape at its press bottom dead center with little springback and the like), and making the steel sheet prone to springback. - It could thus be helpful by this disclosure to provide a method of manufacturing a hot press-formed part that can suppress a reduction in the shape fixability during hot press forming while preventing micro-cracks, when producing a hot press-formed part by hot press forming of a coated steel sheet having a Zn-Ni-based plating layer formed thereon. It could also be helpful to provide a hot press-formed part produced with the method.
- Firstly, we investigated how to suppress micro-cracks (microfissures) which would otherwise occur during hot press forming of a steel sheet coated with Zn or a zinc-based alloy.
Although the micro-crack occurrence mechanism is still unclear, press forming of a steel sheet coated with Zn or a zinc-based alloy at high temperature at or below the freezing point of the plating layer may cause microfissures in the surface of the steel sheet. Similar microfissures also occur in a Zn-Ni coated steel sheet during press forming. Such microfissures are about 30 µm in depth from the interface between the plating layer and the steel sheet, and pass through the interface between the plating layer and the steel sheet and reach the inside of the steel sheet.
As a result of making various researches on this problem, we discovered that micro-cracks are suppressed by keeping the steel sheet at low temperature during hot press forming. Further, by keeping the steel sheet at low temperature during press forming as mentioned above, the effect of significantly reducing the coating weight attached to the tool of press forming, which would be quite large to cause problems with conventional coated steel sheets for hot press forming, was obtained. - However, lowering the temperature of the steel sheet during press forming leads to an increase in the strength of the steel sheet and thus causes lower shape fixability, which could cancel the advantage of hot press forming. We thus conceived cooling, before performing hot press forming, only those portions of the steel sheet that are subjected to forming that would cause micro-cracks during the press forming. We then studied what forming would cause micro-cracks and which part would be subjected to such forming. Firstly, in our studies on forming that could cause micro-cracks, we investigated the influences of forming strain upon the occurrence of micro-cracks. As a result, it was discovered that micro-cracks are not caused by compressive deformation or bending deformation alone, but are caused at those portions that are subjected to deformation resulting from bending and subsequent bend restoration.
To this extent, forming as described above may limited to a particular range, but in some cases the portions of the steel sheet subjected to forming that would cause micro-cracks may be extensive depending on the shape of the formed part. - Accordingly, we investigated how to suppress the occurrence of micro-cracks throughout, rather than in a limited range of, a steel sheet as a press forming sheet. As a result, it was discovered that by cooling the heated coated steel sheet to a temperature of 550 °C or lower and 410 °C or higher, at a cooling rate of 100 °C/s or higher, by squeezing the heated coated steel sheet with a press tool for cooling having flat surfaces configured to contact the coated steel sheet, and by starting press forming of the coated steel sheet with a tool of press forming within 5 seconds after the cooling while the temperature of the coated steel sheet is 550 °C or lower and 400 °C or higher, it becomes possible to suppress the occurrence of micro-cracks throughout both front and back surfaces of the resulting press formed part, while preventing loss of shape accuracy.
- The reason why such cooling using the press tool for cooling prevented loss of shape accuracy is thought to be as follows.
For hat-shaped section parts, typical defects in shape accuracy include angle change such that the angle formed by two faces across the bending ridgeline becomes large relative to the angle of the tool of press forming, and wall camber such that the planes of the wall portions have curvature. Both of these defects occur due to the difference of any stress distribution in the sheet thickness direction, and the higher the flow stress of the steel sheet during forming, the difference becomes more significant and the shape accuracy decreases. In other words, in hot press forming, as the press forming temperature becomes lower, flow stress in the steel sheet during the press forming increases and shape accuracy decreases. As a result of cooling, the temperature of the steel sheet would become lower at the time of press forming and shape accuracy would degrade. However, when the steel sheet was cooled to a temperature of 550 °C or lower and 410 °C or higher at a cooling rate of 100 °C/s or higher, and when press forming of the steel sheet was started within 5 seconds after the cooling while the temperature of the steel sheet was 550 °C or lower and 400 °C or higher, there was almost no loss of shape accuracy. - The reason is considered to be that when the heated steel sheet is quenched with the press tool for cooling and subjected to press forming while the steel sheet temperature is 550 °C or lower and 400 °C or higher, the steel sheet has a microstructure of austenite during the press forming, and austenite transforms to martensite after the press forming, thereby relieving the stress accumulating during the press forming.
- In contrast, if the press forming start temperature is decreased without quenching the heated steel sheet, ferrite and bainite are formed before the start of press forming, which is believed to cause a decrease in strength and the above-described angle change.
- In addition, if press forming is started while the steel sheet temperature is below 400 °C, martensitic transformation would already begin before the start of press forming, and the above-described wall camber would be caused by the stress accumulating during the press forming in combination with increased steel sheet strength.
- This disclosure is based on the aforementioned discoveries. Thus, the present invention provides a method of manufacturing a hot press-formed part according to
claims - According to the present invention, it becomes possible to provide hot press-formed parts, using coated steel sheets as steel sheets, that are free from micro-cracks throughout both front and back surfaces and that have sufficient hardness and satisfactory shape fixability without a significant increase in press forming load, and thus to manufacture automotive parts and the like in a variety of product shapes using coated steel sheets with high strength.
- In the accompanying drawings:
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FIG. 1 illustrates a method for manufacturing a hot press-formed part according to one of the disclosed embodiments; -
FIGS. 2A and 2B are first schematic diagrams, each illustrating the relationship between metallographic structure, temperature, and cooling time; -
FIG. 3 is a second schematic diagram illustrating the relationship between metallographic structure, temperature, and cooling time; -
FIG. 4 illustrates a test piece used in experiments according to one of the disclosed embodiments; -
FIG. 5 is a graph illustrating experimental results according to one of the disclosed embodiments, showing the change in temperature of the test piece; -
FIG. 6 is a partial enlarged view ofFIG. 5 , with emphasis on the horizontal axis; -
FIGS. 7A-7C show SEM images of wall portions of press formed parts, demonstrating experimental results according to embodiments of the disclosure; -
FIG. 8 is a graph illustrating experimental results according to one of the disclosed embodiments, showing the relationship between press forming start temperature and press forming load; -
FIG. 9 is a graph illustrating experimental results according to one of the disclosed embodiments, showing the relationship between press forming start temperature and amount of mouth opening deformation; -
FIGS. 10A and 10B illustrate forming methods according to embodiments of the disclosure; -
FIG. 11 illustrates a press formed part to be press formed in examples; -
FIG. 12 is a diagram for explaining a micro-crack examined in examples; and -
FIG. 13 illustrates the amount of mouth opening deformation examined in examples. - In one of the disclosed embodiment, a method of manufacturing a hot press-formed part by hot pressing a
coated steel sheet 1 formed with a Zn-Ni plating layer on a surface of a steel sheet as illustrated inFIG. 1 , comprises: heating (not shown) the coatedsteel sheet 1 to a temperature range of Ac3 transformation temperature to 1000 °C; cooling (S1) the heated coated steel sheet I to a temperature of 550 °C or lower and 410 °C or higher, at a cooling rate of 100 °C/s or higher, by squeezing the coatedsteel sheet 1 with a press tool for cooling 3 having flat surfaces configured to contact the coatedsteel sheet 1; starting (S2) press forming of the coatedsteel sheet 1 with a tool of press forming 11 within 5 seconds after the cooling while the temperature of the coatedsteel sheet 1 is 550 °C or lower and 400 °C or higher, to obtain a formed body 1'; and quenching (S3) the formed body 1', while squeezing the formed body with the tool of press forming 11 and holding at its press bottom dead center, to obtain a hot press-formed part.
The following provides details of the material of a hot press-formed part, and the steps of heating, cooling (S1), press forming (S2), and quenching (S3) performed thereon. - As the material of a hot press-formed part, a coated steel sheet formed with a Zn-Ni plating layer on a surface of a steel sheet is used. The provision of a Zn-Ni plating layer on a surface of the steel sheet ensures the corrosion resistance of the part after subjection to hot press forming.
- The method of forming a Zn-Ni plating layer on a surface of the steel sheet is not particularly limited, and any methods such as hot-dip galvanizing and electrogalvanizing may be used. The coating weight per side is preferably 10 g/m2 or more and 90 g/m2 or less.
- The Ni content in the plating layer is preferably 9 mass% or more and 25 mass% or less. In the case of forming a Zn-Ni plating layer on a surface of the steel sheet by electrogalvanizing, a γ phase having any of the crystal structures of Ni2Zn11, NiZn3, or Ni5Zn21 is formed when the Ni content in the plating layer is 9 mass% or more and 25 mass% or less. The γ phase has a high melting point, and thus is advantageous in preventing the plating layer from evaporating when heating the coated steel sheet before subjection to hot press forming. The γ phase is also advantageous in suppressing liquid metal embrittlement cracking during high-temperature hot press forming.
- The coated
steel sheet 1 is heated to a temperature range of Ac3 transformation temperature to 1000 °C. If the heating temperature of the coated steel sheet I is below Ac3 transformation temperature, a sufficient amount of austenite cannot be obtained during heating, leading to the presence of ferrite during press forming. As a result, it becomes difficult to obtain sufficient strength or good shape fixability through hot press forming. When the heating temperature of the coatedsteel sheet 1 exceeds 1000 °C, on the other hand, the plating layer evaporates or excessive oxide generation occurs in the surface layer part, as a result of which the oxidation resistance or the corrosion resistance of the hot press-formed part decreases. Therefore, the heating temperature is from Ac3 transformation temperature to 1000 °C. More preferably, the heating temperature is from Ac3 transformation temperature + 30 °C to 950 °C. The method of heating the coatedsteel sheet 1 is not particularly limited, and any methods may be used, such as heating in an electric furnace, induction heating furnace, or direct current furnace. - In the cooling (S1), the coated
steel sheet 1 thus heated is cooled to a temperature of 550 °C or lower and 410 °C or higher at a cooling rate of 100 °C/s or higher, by being squeezed with the press tool for cooling 3. - As illustrated in
FIG. 1 , the press tool for cooling 3 comprises anupper cooling tool 5 and alower cooling tool 7, each having a flat surface configured to contact the coatedsteel sheet 1. An extendable lifter pin 9 is provided on thelower cooling tool 7. The heated coatedsteel sheet 1 is placed on the lifter pin 9, and cooled by being squeezed between theupper cooling tool 5 and thelower cooling tool 7. - In general, when squeezing the heated coated
steel sheet 1 with the press tool for cooling 3, both front and back surfaces of the coatedsteel sheet 1 may be squeezed entirely with the press tool for cooling 3 as illustrated inFIG. 1 . However, the coatedsteel sheet 1 may be placed with some portions, such as portions to be trimmed afterwards before finishing operations to form a final product, extending beyond the edges of the press tool for cooling 3. In this way, if portions subjected to forming that would cause micro-cracks, i.e., bending-bend restoration deformation, cover a large area of the coatedsteel sheet 1 as the working material, it is possible to suppress the occurrence of micro-cracks throughout both front and back surfaces of the resulting press formed part. - The temperature at start of squeezing the heated coated steel sheet I with the press tool for cooling 3 is preferably 800 °C or lower from the perspective of preventing the risk of the Zn-Ni plating layer being adhered to the press tool for cooling, and preferably 670 °C or higher from the perspective of guaranteeing the strength after hot press forming. In addition, the coated
steel sheet 1 may be cooled with one surface pressed against the press tool for cooling 3. - In this case, the cooling rate is set to be 100 °C/s or higher because this cooling rate enables the press formed part to have a martensite single phase structure, and thus allows for strengthening, without increasing cost. In the following, this will be described in detail.
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FIG, 2 schematically illustrates the relationship between a typical metallographic structure, temperature, and cooling time when a steel sheet is subjected to hot press forming using a tool of press forming.FIG. 2A shows a case where the press forming start temperature is high and, after the start of press forming, the coated steel sheet is rapidly cooled by heat extraction to the tool of press forming, so as to have a martensite single phase structure. - On the other hand, if the press forming start temperature is low as shown in
FIG. 2B , ferrite and bainite are formed before the start of press forming, leading to a decrease in the strength of the press formed part after subjection to the press forming. - In this way, simply lowering the press forming start temperature ends up in a state as shown in
FIG. 2B . - In contrast, according to the disclosure, by utilizing a cooling process that enables quenching before the start of press forming, a martensite single phase structure can be obtained while lowing the forming start temperature, as indicated by a dashed curve in
FIG. 3 . - The upper limit of the cooling rate is normally around 500 °C/s.
- In the cooling, the cooling stop temperature is set to be 550 °C or lower because, above 550 °C, cooling becomes insufficient, causing micro-cracks after the hot press forming. The cooling stop temperature is preferably 500 °C or lower. In addition, the lower limit of the cooling stop temperature is 410 °C because, below 410 °C, the coated
steel sheet 1 is excessively cooled before subjection to the press forming, leading to deterioration in shape fixability after subjection to the press forming. The cooling stop temperature is preferably 430 °C or higher. - In the cooling, the cooling rate and the cooling stop temperature may be controlled by, for example, varying the time to hold the coated
steel sheet 1 with the press tool for cooling 3 (seeFIG. 1 ). Changes in the temperature of the coatedsteel sheet 1 when squeezed with the press tool for cooling 3 may be determined by measuring the temperature of the coatedsteel sheet 1 using asheath type thermocouple 19 of 0.5 mmφ inserted into the steel sheet in a manner as illustrated inFIG. 4 .FIG. 5 is a graph showing some of the results, where the vertical axis is temperature (°C) and the horizontal axis is time (s).FIG. 6 is a graph representing a partial enlarged view ofFIG. 5 , with emphasis on the horizontal axis, and focusing on an area enclosed by a dashed line inFIG. 5 . It can be seen fromFIG. 6 that the change in temperature during the cooling process with the press tool for cooling was about 160 °C/s, proving the ability to perform quenching. - As an experiment in one embodiment, press formed parts were formed at different conditions by varying the holding time during which the press formed part was being held in the press tool for cooling (in particular, the cooling stop temperature set for the press tool for cooling), and the press forming start temperature, which will be described below, and evaluation was made of the following parameters. For evaluation, observations were made to: (i) verify whether micro-cracks occurred by observing cross sections of wall portions of the press formed parts; (ii) determine the hardness of the press formed parts; (iii) determine the press forming load; and (iv) determine the shape fixability by measuring the amount of mouth opening deformation of hat openings of the press formed parts (the difference between the width of each opening after die release following the press forming and the width of the corresponding press formed part conformed to the tool of press forming).
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FIG. 7 shows SEM (Scanning Electron Microscope) images of cross sections of surface layers, on the side contacting adie 13, of wall portions of press formed parts that were formed at different conditions by varying the time to cool the press formed part in the press tool for cooling (the cooling stop temperature set for the press tool for cooling) and the press forming start temperature. It can be seen fromFIGS. 7A-7C that no micro-cracks were observed in the steel sheets with a cooling time in the press tool for cooling of 0.9 s or more (and a press forming start temperature of 550 °C or lower). Under all conditions, Hv > 450, proving that quench hardenability does not deteriorate. -
FIG. 8 shows the relationship between press forming start temperature and press forming load, where the vertical axis is the press forming load (kN) and the horizontal axis is the press forming start temperature (°C). It can be seen fromFIG. 8 that a reduction in the press forming start temperature caused by the process of cooling in the press tool for cooling prior to press forming caused an increased press forming load, which was, however, equivalent to that on mild steel (270D, cold deep forming) at temperatures around 550 °C at which micro-cracks do not occur, and thus posed no problem. -
FIG. 9 shows the relationship between press forming start temperature and amount of mouth opening deformation, where the vertical axis is the amount of mouth opening deformation (mm) of a formed part and the horizontal axis is the press forming start temperature (°C). As shown inFIG. 9 , the amount of mouth opening deformation increases due to a decrease in the forming start temperature caused by the process of cooling in the press tool for cooling prior to the press forming process, which shows a tendency such that shape fixability deteriorates accordingly. However, up to the point where the press forming start temperature is 400 °C or higher, almost no deterioration of shape fixability is observed. - As described above, by cooling the coated steel sheet by means of a predetermined press tool for cooling to a temperature of 550 °C or lower to 410 °C or higher at a cooling rate of 100 °C/s or higher, and, as described below, by starting press forming of the coated steel sheet within 5 seconds after the cooling while the temperature of the coated steel sheet is 550 °C or lower to 400 °C or higher, it becomes possible to provide a press formed part that is free from micro-cracks and has sufficient hardness and shape fixability without increasing the press forming load.
- In the press forming (S2), the coated
steel sheet 1 is press formed into the shape of a product. The press forming is performed with the tool of press forming 11 after the cooling. The tool of press forming 11 comprises a die 13 and apunch 17 as illustrated inFIG. 1 . The coatedsteel sheet 1 is press formed by being squeezed between the die 13 and thepunch 17, to obtain a formed body 1'. - As described above, it is possible to manufacture a press formed part that is free from micro-cracks and has sufficient hardness and shape fixability, without increasing the press forming load, by, in the cooling, cooling the coated
steel sheet 1 in the press tool for cooling 3 to a temperature of 550 °C or lower and 410 °C or higher at a cooling rate of 100 °C/s or higher, then removing the coatedsteel sheet 1 from the press tool for cooling 3, and starting press forming while the temperature of the coatedsteel sheet 1 is 550 °C or lower and 400 °C or higher.
The press forming is started within 5 seconds after the cooling because, if press forming is started after expiry of the time limit of 5 seconds after the cooling, for example, ferrite and bainite are formed before the start of press forming, preventing formation of a martensite single phase structure. As a result, the press formed part has insufficient hardness. Press forming is preferably started within 3 seconds after the cooling. No lower limit is particularly placed on the time limit, yet a preferred time limit is normally 1 second or more. - The present disclosure is not limited to a particular press forming method. However, available methods include, for example, draw forming whereby the coated
steel sheet 1 is subjected to forming while being squeezed between the die 13 and theblank holder 15 as illustrated inFIG. 10A , and crash forming whereby the coatedsteel sheet 1 is subjected to forming while lowering theblank holder 15, or alternatively, without using theblank holder 15, as illustrated inFIG. 10B . From the perspective of suppressing micro-cracks, crash forming is preferred because of less excessive forming of wall portions of the press formed part. - In the quenching (S3), which follows the press forming, the formed body 1' is quenched while being squeezed and held in the tool of press forming 11, to obtain a hot press-formed part. In order for the formed body 1' to be quenched with the tool of press forming 11 after the press forming, the press slide of the formed body 1' is stopped at its press bottom dead center after subjection to the press forming. The sliding stop time is preferably 3 seconds or more, although it varies with the amount of heat released by the tool of press forming. No upper limit is particularly placed on the sliding stop time, yet it is preferably 20 seconds or less from the perspective of productivity.
- In order for a steel sheet to be held in the tool of press forming for a predetermined period of time to have a quenched microstructure, it is possible to use a hot-rolled or cold-rolled steel sheet having a chemical composition containing (consisting of), for example, in mass%, C: 0.15 % or more and 0.50 % or less, Si: 0.05 % or more and 2.00 % or less, Mn: 0.50 % or more and 3.00 % or less, P: 0.10 % or less, S: 0.050 % or less, Al: 0.10 % or less, and N: 0.010 % or less, and the balance consisting of Fe and unavoidable impurities. The following provides a description of the chemical composition. When the composition is expressed in "%", this refers to "mass%" unless otherwise specified.
- C is an element that improves the strength of steel. To increase the strength of the hot pressed part, the C content is preferably 0.15 % or more. When the C content exceeds 0.50 %, on the other hand, the weldability of the hot press-formed part and the fine blanking workability of the material (steel sheet) decrease significantly. Accordingly, the C content is preferably 0.15 % or more and 0.50 % or less, and more preferably 0.20 % or more and 0.40 % or less.
- Si is an element that improves the strength of steel, as with C. To increase the strength of the hot pressed part, the Si content is preferably 0.05 % or more. When the Si content exceeds 2.00 %, on the other hand, a surface defect, called red scale, increases significantly during hot rolling for manufacturing a steel sheet. Accordingly, the Si content is preferably 0.05 % or more and 2.00 % or less, and more preferably 0.10 % or more and 1.50 % or less.
- Mn is an element that enhances the quench hardenability of steel, and is effective in suppressing the ferrite transformation of the steel sheet and improving quench hardenability in the cooling process after the hot press forming. Mn also has a function of lowering the Ac3 transformation temperature, and thus is an element effective in lowering the heating temperature of the coated
steel sheet 1 before subjection to hot press forming. To achieve these effects, the Mn content is preferably 0.50 % or more. When the Mn content exceeds 3.00 %, on the other hand, Mn segregation occurs, reducing the uniformity of characteristics of the steel sheet and of the hot press-formed part. Accordingly, the Mn content is preferably 0.50 % or more and 3.00 % or less, and more preferably 0.75 % or more and 2.50 % or less. - When the P content exceeds 0.10 %, P segregates to grain boundaries, reducing the low-temperature toughness of the steel sheet and of the hot press-formed part. Accordingly, the P content is preferably 0.10 % or less, and more preferably 0.01 % or less. Excessively reducing the P content, however, leads to increased cost in the steelmaking process. Therefore, the P content is preferably 0.003 % or more.
- S is an element that forms a coarse sulfide by combining with Mn and causes a decrease in ductility of steel. The S content is preferably reduced as much as possible, though up to 0.050 % is allowable. Accordingly, the S content is preferably 0.050 % or less, and more preferably 0,010 % or less. Excessively reducing the S content, however, leads to increased cost of desulfurization in the steelmaking process. Therefore, the S content is preferably 0.0005 % or more.
- When the Al content exceeds 0.10 %, oxide inclusions in steel increase, and the ductility of steel decreases. Accordingly, the Al content is preferably 0.10 % or less, and more preferably 0.07 % or less. Al functions as a deoxidation material, however, and from the perspective of improving the cleanliness factor of steel, the Al content is preferably 0.01 % or more.
- When the N content exceeds 0.010 %, nitrides such as AIN form in the steel sheet, which causes lower formability during hot press forming. Accordingly, the N content is preferably 0.010 % or less, and more preferably 0.005 % or less. Excessively reducing the N content, however, leads to increased cost in the steelmaking process. Therefore, the N content is preferably 0.001 % or more.
- While preferable basic components of the steel sheet used in the method according to the disclosure have been described, the steel sheet may further contain one or more of the following elements as necessary:
- Cr, V, Mo, and Ni are each an element effective in enhancing the quench hardenability of steel. This effect is achieved when the content of any of these elements contained is 0.01 % or more. However, adding any of Cr, V, Mo, or Ni beyond 0.50 % fails to further increase this effect, but instead increases cost. Accordingly, in the case where one or more of Cr, V, Mo, and Ni is included, the content is preferably 0.01 % or more and 0.50 % or less, and more preferably 0,10 % or more and 0.40 % or less.
- Ti is effective for strengthening steel. The strengthening effect of Ti is achieved when the content is 0.01 % or more. Ti can be used to strengthen steel without any problem as long as the content is within the range specified herein. However, adding Ti beyond 0.20 % fails to increase this effect, but instead increases cost. Accordingly, in the case where Ti is included, the content is preferably 0.01 % or more and 0.20 % or less, and more preferably 0.01 % or more and 0.05 % or less.
- Nb is also effective for strengthening steel. The strengthening effect of Nb is achieved when the content is 0.01 % or more. Nb can be used to strengthen steel without any problem as long as the content is within the range specified herein. However, adding Nb beyond 0.10 % fails to increase this effect, but instead increases cost. Accordingly, in the case where Nb is included, the content is preferably 0.01 % or more and 0.10 % or less, and more preferably 0.01 % or more and 0.05 % or less.
- B is an element that enhances the quench hardenability of steel, and is effective in suppressing the generation of ferrite from austenite grain boundaries and obtaining a quenched microstructure when cooling the steel sheet after subjection to the hot press forming. This effect is achieved when the B content is 0.0002 % or more. However, adding B beyond 0.0050 % fails to increase this effect, but instead increases cost. Accordingly, in the case where B is included, the content is preferably 0.0002 % or more and 0.0050 % or less, and more preferably 0.0005 % or more and 0.0030 % or less.
- Sb has the effect of suppressing generation of a decarburized layer in the surface layer part of the steel sheet during the period from when a steel sheet is heated before subjection to hot press forming to when the steel sheet is cooled through a series of hot press forming processes. To obtain this effect, the Sb content is preferably 0.003 % or more. When the Sb content exceeds 0.030 %, however, the rolling load increases during steel sheet manufacture, which may cause lower productivity. Accordingly, in the case where Sb is included, the content is preferably 0.003 % or more and 0.030 % or less, and more preferably 0.005 % or more and 0.010 % or less.
- The components (balance) other than the above are Fe and unavoidable impurities.
- The manufacturing conditions of the coated
steel sheet 1 used as the material of the hot press-formed part are not particularly limited. For example, the steel sheet may be a hot-rolled steel sheet (pickled steel sheet) having a predetermined chemical composition or a cold-rolled steel sheet obtained by subjecting the hot-rolled steel sheet to cold rolling. - The formation of a Zn-Ni plating layer on a surface of the steel sheet for obtaining the coated
steel sheet 1 is not limited to particular conditions. In the case where a hot-rolled steel sheet (pickled steel sheet) is used as the steel sheet, the coatedsteel sheet 1 may be obtained by subjecting the hot-rolled steel sheet (pickled steel sheet) to Zn-Ni coating treatment. - In the case where a cold-rolled steel sheet is used as the steel sheet, the coated
steel sheet 1 may be obtained by subjecting the cold-rolled steel sheet to Zn-Ni coating treatment either directly after subjection to the cold rolling, or after subjection to annealing treatment following the cold rolling. - In the case of forming a Zn-Ni plating layer on a surface of the steel sheet, for example, the Zn-Ni plating layer may be formed by degreasing and pickling the steel sheet, and then subjecting the steel sheet to electrogalvanizing treatment with a current density of 10 A/dm2 or more and 150 A/dm2 or less, in a plating bath which has a pH of 1.0 or more and 3.0 or less and a bath temperature of 30 °C or higher and 70 °C or lower, and which contains 100 g/L or more and 400 g/L or less nickel sulfate hexahydrate and 10 g/L or more and 400 g/L or less zinc sulfate heptahydrate.
In the case where a cold-rolled steel sheet is used as the steel sheet, the cold-rolled steel sheet may be subjected to annealing treatment before subjection to the degreasing and pickling. The Ni content in the plating layer may be set within the desired range (for example, 9 mass% to 25 mass%) by appropriately adjusting the concentration of zinc sulfate heptahydrate or the current density within the above-mentioned range. The coating weight of the Zn-Ni plating layer may be set within the desired range (for example, 10 g/m2 to 90 g/m2 per side) by adjusting the energizing time. - The following provides a description of experiments, which were conducted to confirm the effect of the method of manufacturing a hot press-formed part disclosed herein.
- Steels having the compositions shown in Table 1 were each smelted into a cast slab, and the cast slab was heated to 1200 °C, hot rolled with a finish rolling completion temperature of 870 °C, and coiled at 600 °C to obtain a hot-rolled steel sheet.
-
Table 1 Steel Chemical Composition (mass%) Ac1 transformation temperature (°C) C Si Mn P S Al N B Sb A 0.23 0.32 1.75 0.01 0.005 0.02 0.003 - - 789 B 0.31 0.15 1.32 0.01 0,005 0.03 0.003 - - 783 C 0.19 0.95 2.35 0.03 0,007 0.02 0.004 - - 822 D 0.21 0.20 1.80 0.01 0.003 0.03 0.004 0.0020 0.010 791 - The hot-rolled steel sheet was then pickled and cold rolled with a reduction of 50 %, to obtain a cold-rolled steel sheet with a thickness of 1.6 mm. The Ac3 transformation temperature in Table 1 was calculated by Formula (1) below (see William C. Leslie, "The Physical Metallurgy of Steels", translation supervised by Nariyasu Kouda, translated by Hiroshi Kumai and Tatsuhiko Noda, Maruzen Co., Ltd., 1985, p. 273 ).
Using each cold-rolled steel sheet thus obtained as a steel sheet, a pure Zn plating layer, a Zn-Fe plating layer, or a Zn-Ni plating layer was formed on a surface of the steel sheet to obtain acoated steel sheet 1. Each plating layer was formed under the following conditions. - A cold-rolled steel sheet was passed through a continuous hot-dip galvanizing line, heated to a temperature range of 800 °C to 900 °C at a heating rate of 10 °C/s, and held in this temperature range for 10 s or more and 120 s or less. Subsequently, the cold-rolled steel sheet was cooled to a temperature range of 460 °C to 500 °C at a cooling rate of 15 °C/s, and dipped into a galvanizing bath at 450 °C to form a Zn plating layer. The coating weight of the Zn plating layer was adjusted to a predetermined coating weight using a gas wiping method.
- A cold-rolled steel sheet was passed through a continuous hot-dip galvanizing line, heated to a temperature range of 800 °C to 900 °C at a heating rate of 10 °C/s, and held in this temperature range for 10 s or more and 120 s or less. Subsequently, the cold-rolled steel sheet was cooled to a temperature range of 460 °C to 500 °C at a cooling rate of 15 °C/s, and dipped into a galvanizing bath at 450 °C to form a Zn plating layer. The coating weight of the Zn plating layer was adjusted to a predetermined coating weight using a gas wiping method. As soon as the Zn plating layer was adjusted to the predetermined coating weight using the gas wiping method, the cold rolled steel sheet was heated to a temperature range of 500 °C to 550 °C and held for 5 s to 60 s in an alloying furnace, thereby forming a Zn-Fe plating layer. The Fe content in the plating layer was set to a predetermined content by changing the heating temperature in the alloying furnace and the holding time at the heating temperature within the above-mentioned ranges.
- The cold-rolled steel sheet was passed through a continuous annealing line, heated to a temperature range of 800 °C to 900 °C at a heating rate of 10 °C/s, and held in this temperature range for 10 s or more and 120 s or less. Subsequently, the cold-rolled steel sheet was cooled to a temperature range of 500 °C or lower at a cooling rate of 15 °C/s. Then, the cold-rolled steel sheet was subjected to degreasing and pickling, followed by electrogalvanizing treatment whereby the cold-rolled steel sheet was energized for 10 s to 100 s with a current density of 30 A/dm2 to 100 A/dm2, in a plating bath containing 200 g/L nickel sulfate hexahydrate and 10 g/L to 300 g/L zinc sulfate heptahydrate and having a pH of 1.3 and a
bath temperature 50 °C, thereby forming a Zn-Ni plating layer. The Ni content in the plating layer was set to a predetermined content by appropriately adjusting the concentration of zinc sulfate heptahydrate and the current density within the above-mentioned ranges. The coating weight of the Zn-Ni plating layer was set to a predetermined coating weight by appropriately adjusting the energizing time within the above-mentioned range. - A blank sheet of 200 mm × 400 mm was blanked from each coated steel sheet thus obtained, and heated in an electric furnace in air atmosphere. The blank sheet was then placed and cooled in a press tool for cooling (material: SKD61), and subjected to press forming and quenching using a tool of press forming under the conditions presented in Table 2. After being quenched, the blank sheet was released from the tool of press forming to manufacture a press formed part with a hat-shaped section as illustrated in
FIG. 11 . Regarding the size of the tool of press forming, the round portion of punch shoulder was 6 mm and the round portion of die shoulder was 6 mm. The press forming was performed with a punch-die clearance of 1.6 mm. Cooling prior to press forming was performed by bringing the blank sheet into contact with the press tool for cooling. Press forming was performed either by draw forming under a blank holder force of 98 kN, or crash forming without using a blank holder. - Table 2 shows the blank sheet heating temperature, type of steel sheet, type of plating layer, heating conditions, cooling conditions, and press forming conditions.
- A sample was collected from a wall portion of each press formed part having a hat-shaped section, and a cross section of the surface was observed under a scanning electron microscope (SEM) at 1000 times magnification over ten fields per sample to examine the presence or absence of micro-cracks (microfissures in the surface of the sample, which pass through the interface between the plating layer and the steel sheet and reach the inside of the steel sheet) and the average depth of any micro-cracks. The average depth of micro-cracks was determined by averaging the micro-crack depths of arbitrarily selected 20 micro-cracks. As used herein, a "micro-crack depth" refers to, as illustrated in
FIG. 12 , the length of a micro-crack 21 measured from the interface between aplating layer 23 and asteel sheet 25 toward the center in the thickness direction (as indicated by length h inFIG. 12 ). In the case where the number of microcracks observed was less than 20, the average of the depths of all the observed micro-cracks was used.
The shape accuracy of each press formed part was evaluated based on the amount of mouth opening deformation, which was determined by the difference (W - W0) between the width (W) of each press formed part with a hat-shaped section after die release and the width (W0) of the corresponding formed part when conformed to the shape of the tool of press forming illustrated inFIG. 13 . - Table 2 also lists these results.
- Additionally, a sample for hardness measurement was collected from a wall portion of each press formed part with a hat-shaped section. The hardness of the cross section of each sample was measured using a micro-Vickers hardness meter. A test was conducted with a test load of 9.8 N, and hardness measurement was made at five central positions in the thickness direction for each sample, and the average was used as the hardness of the sample. In this case, the targeted hardness was 400 Hv or more. Additionally, a JIS No. 13 B tensile test piece was collected from a wall portion of each press formed part with a hat-shaped section. A tensile test was conducted on each test piece thus collected according to JIS G 0567 (1998), and measurement was made of the tensile strength at room temperature (22 ± 5 °C). Note that all of the tensile tests were conducted with a cross-head speed of 10 mm/min. In this case, the targeted tensile strength was 1180 MPa or more.
Table 2 also lists these results.[Table 2] Table 2 Steel Plating layer Heating Conditions Cooling conditions Press forming conditions Evaluation results Remarks Type Coating weight (g/m2) Heating temp. (°C) Holding time (s) Cooling method Cooling start temp. (°C) Cooling time (s) Cooling rate (°C/s) Cooling stop temp. (°C) Forming method Time limit to start press forming after cooling (s) Press forming start temp. (°C) Holding time at press bottom dead center (s) Steel sheet surface Amount of mouth opening deformation (mm) Hardness (Hv) Tensile strength (MPa) Cracks Average depth of cracks (µm) Zn-10Ni% 60 880 10 Cooling in press tool for cooling 700 0.9 189 530 Crash forming 2 525 10 Not occurred - 0 478 1514 Example 1 Zn-I2M% 45 900 30 Cooling in press tool for cooling 740 1.1 218 500 Draw forming 2 495 12 Not occurred - 0 470 1493 Example 2 Zn-21Ni% 30 920 5 Cooling in press tool for cooling 720 1.7 159 450 Draw forming 3 442 15 Not occurred - 0 485 1528 Example 3 Zn-15Ni% 55 900 120 Cooling in press tool for cooling 650 1.1 155 480 Crash forming 3 472 8 Not occurred - 0 487 1545 Example 4 Zn-15%Ni 55 920 15 Cooling in press tool for cooling; 700 1.0 180 520 Draw forming 3 512 12 Not occurred - 0 480 1520 Example 5 A Zn-12Ni% 45 850 20 Cooling in press tool for cooling 770 1.2 225 500 Crash forming 5 487 15 Not occurred - 0 498 1573 Example 6 Zn-12Ni% 45 880 5 Cooling in press tool for cooling 640 0.6 167 540 Crash forming 3 532 10 Not occurred - 0 473 1499 Example 7 Zn-12Ni% 45 920 60 - - - - - Crash forming - 720 15 Occurred 8 0 481 1520 Comparative Example 1 Zn-10Ni% 60 900 90 Cooling in press tool for cooling 680 0.4 200 600 Draw forming 3 592 15 Occurred 12 0 471 1491 Comparative Example 2 Zu-21Ni% 45 880 20 Cooling in press tool for cooling 700 3.5 103 340 Draw forming 2 335 12 Not occurred - 8 502 1581 Comparative Example 3 Zn-14Ni% 55 900 30 Cooling in press tool for cooling 740 4.9 92 290 Crash forming 2 285 10 Not occurred - 9 500 1580 Comparative Example 4 Steel Plating layer Heating Conditions Cooling conditions Press forming conditions Evaluation results Remarks Type Coating weight (g/m2) Heating temp. (°C) Holding time (s) Cooling method Cooling start temp. (°C) Cooling time (s) Cooling rate (°C/s) Cooling stop temp. (°C) Forming method Time limit to press forming after cooling (s) Press forming start temp. (°C) Holding time at press bottom dead center (s) Steel sheet surface Amount of mouth opening deformation (mm) Hardness (Hv) Tensile strength (MPa) Cracks Average depth of cracks (µm) Zn-12Ni% 45 900 10 Gas cooling 700 1.8 22 660 Draw forming 2 655 15 Occurred 13 0 467 1473 Comparative Example 5 Zn-12Ni% 45 880 20 Gas cooling 720 4.8 27 590 Crash forming 2 585 10 Occurred 7 2 376 1171 Comparative Example 6 Zn-10%Ni 60 910 10 Gas cooling 680 10.5 16 510 Crash forming 3 502 10 Not occurred - 3 345 1104 Comparative Example 7 A Zn-12%Ni 45 900 10 Cooling in press tool for cooling 710 1.0 180 530 Draw forming 10 505 15 Not occurred - 2 365 1155 Comparative Example 8 Zn-1:%Ni 55 890 20 Cooling in press tool for cooling 670 1.5 153 440 Crash forming 8 420 15 Not occurred - 2 382 1162 Comparative Example 9 Zn 50 900 20 Cooling in press tool for cooling 700 1.2 167 500 Crash forming 2 495 15 Occurred 31 0 480 1510 Comparative Example 10 Zn-10Fe% 40 880 10 Cooling in press tool for cooling 720 1.0 190 530 Draw forming 2 525 15 Occurred 5 0 488 1545 Comparative Example 11 B Zn-12Ni% 60 900 60 Cooling in press tool for cooling 700 1.2 167 500 Crash forming 2 495 Not occurred - 0 543 1620 Example 8 C Zn-10Ni% 50 890 30 Cooling in press tool for cooling 680 1.0 160 520 Draw forming 3 512 3 Not occurred - 0 436 1420 Example 9 D Zn-12Ni% 50 900 20 Cooling in press tool for cooling 700 1.0 180 520 Draw forming 3 520 15 Not occurred - 0 475 1505 Example 10 - In examples 1 to 10, the type of plating layer (Zn-Ni plating layer), cooling process (cooling in the press tool for cooling), cooling time (0.6 s to 1.7 s), cooling rate (appropriate range: 100 °C/s or higher), cooling stop temperature (appropriate range: 410 °C to 550 °C), time limit to start press forming after cooling (appropriate range: within 5 seconds), and press forming start temperature (appropriate range: 400 °C to 550 °C) are all within the appropriate ranges specified in this disclosure. The pressed samples according to our examples were free from micro-cracks, and the amount of mouth opening deformation was determined to be 0 mm for these samples. From these results, it can be seen that, with the press forming process disclosed herein, it is possible to suppress the occurrence of micro-cracks while ensuring good shape fixability.
- In contrast, Comparative Example 1 was subjected to a forming process without being cooled with the press tool for cooling. Comparative Examples 2 to 4 were outside the appropriate range (410 °C to 550 °C) in terms of cooling stop temperature. Specifically, the cooling stop temperature was 600 °C in Comparative Example 2, 340 °C in Comparative Example 3, and 290 °C in Comparative Example 4.
- In Comparative Examples 1 and 2, micro-cracks occurred, although the amount of mouth opening deformation was 0 mm. From this follows that micro-cracks will occur in a steel sheet when the forming start temperature of the steel sheet is higher than 550 °C.
- In Comparative Examples 3 and 4, micro-cracks did not occur, yet the amount of mouth opening deformation was 8 mm to 10 mm. From these results, it can be seen that if the cooling time is excessively long and the cooling stop temperature of the steel sheet is below 410 °C, then the press forming start temperature is below 400 °C, which causes an increase in the strength of the steel sheet and thus a reduction in the shape fixability.
- In Comparative Examples 5 to 7, the cooling process was gas cooling, in which the cooling rate was outside the appropriate range (100 °C/s or higher), and thus rapid cooling could not be performed. Accordingly, in Comparative Examples 5 and 6, the cooling stop temperature and the press forming start temperature of the steel sheets were outside the appropriate ranges (cooling stop temperature: 410 °C to 550 °C, press forming start temperature: 400 °C to 550 °C), and micro-cracks occurred. Further, in Comparative Example 7, the cooling stop temperature was 510 °C, which is within the appropriate range. However, the amount of mouth opening deformation was 3 mm, which shows a reduction in the shape fixability. The reason is believed to be that due to a low cooling rate of gas cooling, the angle formed by two faces of the press formed part across a bend ridgeline was larger than the angle of the tool of press forming.
Moreover, in Comparative Examples 6 and 7, the steel sheets were quenched after being mild cooled to some extent by gas cooling and subjected to press forming, and thus showed a reduction in the hardness and tensile strength after subjection to the press forming. - In Comparative Examples 8 and 9, press forming was started in 10 seconds and 8 seconds respectively after the cooling, exceeding the appropriate time limit of 5 seconds. Accordingly, in Comparative Examples 8 and 9, the amount of mouth opening deformation was 2 mm, and the steel sheets showed a reduction in the hardness and tensile strength after subjection to the press forming.
- Comparative Examples 10 and 11 were different from the examples and other comparative examples in the type of plating layer. Specifically, Comparative Example 10 used a pure Zn plating layer and Comparative Example 11 used a Zn-Fe plating layer. The press forming start temperature at which micro-cracks will not occur in the pure Zn plating layer or in the Zn-Fe plating layer is even lower than the press forming start temperature at which micro-cracks will not occur in a Zn-Ni plating layer. Thus, micro-cracks occurred in Comparative Examples 10 and 11.
-
- 1
- Coated steel sheet
- 1'
- Formed body
- 3
- Press tool for cooling
- 5
- Upper cooling tool
- 7
- Lower cooling tool
- 9
- Lifter pin
- 11
- Tool of press forming
- 13
- Die
- 15
- Blank holder
- 17
- Punch
- 19
- Thermocouple
- 21
- Micro-crack
- 23
- Plating layer
- 25
- Steel sheet
Claims (2)
- A method of manufacturing a hot press-formed part by hot pressing a coated steel sheet (1) formed with a Zn-Ni plating layer (23) on a surface of a steel sheet (25), wherein the steel sheet (25) has a chemical composition consisting of, in mass%, C: 0.15 % or more and 0.50 % or less, Si: 0.05 % or more and 2.00 % or less, Mn: 0.50 % or more and 3.00 % or less, P: 0.10 % or less, S: 0.050 % or less, Al: 0.10 % or less, and N: 0.010 % or less, optionally one or more of Cr: 0.01 % or more and 0.50 % or less, V: 0.01 % or more and 0.50 % or less, Mo: 0.01 % or more and 0.50 % or less, Ni: 0.01 % or more and 0.50 % or less, Ti: 0.01 % or more and 0.20 % or less, Nb: 0.01 % or more and 0.10 % or less, B: 0.0002 % or more and 0.0050 % or less, and Sb: 0.003 % or more and 0.030 % or less, and the balance consisting of Fe and unavoidable impurities, the method comprising:heating the coated steel sheet (1) to a temperature range of Ac3 transformation temperature to 1000 °C;cooling the heated coated steel sheet to a temperature of 550 °C or lower and 410 °C or higher, at a cooling rate of 100 °C/s or higher, by squeezing the coated steel sheet (1) with a cooling press tool (3), wherein the cooling press tool (3) comprises an upper cooling tool (5) and a lower cooling tool (7), each having a flat surface configured to contact the coated steel sheet (1) and wherein both front and back surfaces of the coated steel sheet (1) are squeezed entirely with the cooling press tool (3);press forming the coated steel sheet (1) by squeezing the steel sheet (1) between a die (13) and a punch (17) of a press forming tool (11) to obtain a formed body (1'), the press forming being initiated within 5 seconds after the cooling while the temperature of the coated steel sheet (1) is 550 °C or lower and 400 °C or higher; andquenching the formed body (1'), while squeezing the formed body (1') with the press forming tool (11) and holding at its press bottom dead center, to obtain a hot press-formed part.
- The method of manufacturing a hot press-formed part according to claim 1, characterized in that the Zn-Ni plating layer (23) of the coated steel sheet (1) contains 9 mass% or more and 25 mass% or less of Ni.
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JP2014195530A JP6152836B2 (en) | 2014-09-25 | 2014-09-25 | Manufacturing method of hot press-formed product |
PCT/JP2015/004533 WO2016047058A1 (en) | 2014-09-25 | 2015-09-07 | Method of manufacturing hot press-formed product, and hot press-formed product |
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CN111936248B (en) * | 2018-04-13 | 2022-08-30 | 日本制铁株式会社 | Method for manufacturing hot press-molded product, die and die set |
WO2020158285A1 (en) * | 2019-01-31 | 2020-08-06 | Jfeスチール株式会社 | Hot-pressed member, cold-rolled steel sheet for hot-pressed member, and methods respectively for producing these products |
CN112139335B (en) * | 2020-09-09 | 2022-02-01 | 山东钢铁集团日照有限公司 | Preparation method of high-corrosion-resistance easy-to-weld hot-pressed part |
US11441039B2 (en) * | 2020-12-18 | 2022-09-13 | GM Global Technology Operations LLC | High temperature coatings to mitigate weld cracking in resistance welding |
CN114029699B (en) * | 2021-10-22 | 2022-08-30 | 广东中辉绿建移动房屋科技有限公司 | Preparation method of galvanized roof and integrated house roof |
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SE435527B (en) * | 1973-11-06 | 1984-10-01 | Plannja Ab | PROCEDURE FOR PREPARING A PART OF Hardened Steel |
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FR2807447B1 (en) * | 2000-04-07 | 2002-10-11 | Usinor | METHOD FOR MAKING A PART WITH VERY HIGH MECHANICAL CHARACTERISTICS, SHAPED BY STAMPING, FROM A STRIP OF LAMINATED AND IN PARTICULAR HOT ROLLED AND COATED STEEL SHEET |
JP3896061B2 (en) * | 2002-10-07 | 2007-03-22 | 新日本製鐵株式会社 | Steel sheet with excellent curability after hot forming and method of using the same |
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US7650547B2 (en) | 2007-02-28 | 2010-01-19 | Verigy (Singapore) Pte. Ltd. | Apparatus for locating a defect in a scan chain while testing digital logic |
JP4825882B2 (en) * | 2009-02-03 | 2011-11-30 | トヨタ自動車株式会社 | High-strength quenched molded body and method for producing the same |
PT2290133E (en) * | 2009-08-25 | 2012-06-19 | Thyssenkrupp Steel Europe Ag | Method for producing a steel component with an anti-corrosive metal coating and steel component |
JP4849186B2 (en) * | 2009-10-28 | 2012-01-11 | Jfeスチール株式会社 | Hot pressed member and method for manufacturing the same |
JP4883240B1 (en) * | 2010-08-04 | 2012-02-22 | Jfeスチール株式会社 | Steel sheet for hot press and method for producing hot press member using the same |
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DE102011053941B4 (en) * | 2011-09-26 | 2015-11-05 | Voestalpine Stahl Gmbh | Method for producing hardened components with regions of different hardness and / or ductility |
DE102011053939B4 (en) * | 2011-09-26 | 2015-10-29 | Voestalpine Stahl Gmbh | Method for producing hardened components |
WO2012097976A1 (en) * | 2011-01-17 | 2012-07-26 | Tata Steel Ijmuiden B.V. | Method to produce a hot formed part, and part thus formed |
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