EP3199257A1 - 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 PDF

Info

Publication number
EP3199257A1
EP3199257A1 EP15843885.3A EP15843885A EP3199257A1 EP 3199257 A1 EP3199257 A1 EP 3199257A1 EP 15843885 A EP15843885 A EP 15843885A EP 3199257 A1 EP3199257 A1 EP 3199257A1
Authority
EP
European Patent Office
Prior art keywords
steel sheet
press
cooling
press forming
coated steel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP15843885.3A
Other languages
German (de)
French (fr)
Other versions
EP3199257B1 (en
EP3199257A4 (en
Inventor
Tatsuya Nakagaito
Yuichi Tokita
Toru Minote
Yoshikiyo Tamai
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Steel Corp
Original Assignee
JFE Steel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by JFE Steel Corp filed Critical JFE Steel Corp
Publication of EP3199257A1 publication Critical patent/EP3199257A1/en
Publication of EP3199257A4 publication Critical patent/EP3199257A4/en
Application granted granted Critical
Publication of EP3199257B1 publication Critical patent/EP3199257B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21DWORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21D22/00Shaping without cutting, by stamping, spinning, or deep-drawing
    • B21D22/20Deep-drawing
    • B21D22/208Deep-drawing by heating the blank or deep-drawing associated with heat treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21DWORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21D22/00Shaping without cutting, by stamping, spinning, or deep-drawing
    • B21D22/20Deep-drawing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21DWORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21D22/00Shaping without cutting, by stamping, spinning, or deep-drawing
    • B21D22/20Deep-drawing
    • B21D22/201Work-pieces; preparation of the work-pieces, e.g. lubricating, coating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21DWORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21D24/00Special deep-drawing arrangements in, or in connection with, presses
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21DWORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21D37/00Tools as parts of machines covered by this subclass
    • B21D37/16Heating or cooling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/62Quenching devices
    • C21D1/673Quenching devices for die quenching
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C18/00Alloys based on zinc
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/001Ferrous alloys, e.g. steel alloys containing N
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/002Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/60Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
    • C23C2/022Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
    • C23C2/0224Two or more thermal pretreatments
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
    • C23C2/024Pretreatment of the material to be coated, e.g. for coating on selected surface areas by cleaning or etching
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/06Zinc or cadmium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/26After-treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C30/00Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23FNON-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
    • C23F17/00Multi-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
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/56Electroplating: Baths therefor from solutions of alloys
    • C25D3/565Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of zinc
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/48After-treatment of electroplated surfaces

Definitions

  • This disclosure relates to a hot press-formed part and a method of manufacturing the same, 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.
  • This disclosure also relates to a hot press-formed part produced by the method of manufacturing a hot press-formed part.
  • 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 I 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 l 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.
  • 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
  • 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 ⁇ 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 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.
  • 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 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.
  • 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.
  • 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 1 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 I is heated to a temperature range of Ac 3 transformation temperature to 1000 °C. If the heating temperature of the coated steel sheet 1 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.
  • 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.
  • the press forming start temperature is low as shown in FIG.
  • 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 .
  • 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 I 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 I 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'.
  • 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 coated steel sheet 1 from the press tool for cooling 3, and starting press forming while the temperature of the coated steel 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.
  • 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 A1 content exceeds 0.10 %, oxide inclusions in steel increase, and the ductility of steel decreases. Accordingly, the A1 content is preferably 0.10 % or less, and more preferably 0.07 % or less. A1 functions as a deoxidation material, however, and from the perspective of improving the cleanliness factor of steel, the A1 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:
  • 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.
  • Table 1 Steel Chemical Composition (mass%) Ac 1 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 Ac 3 transformation temperature in Table 1 was calculated by Formula (1) below (see William C. Leslie, "The Pltysical Metallurgy of Steels", translation supervised by Nariyasu Kouda, translated by Hiroshi Kumai and Talsuhiko 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 .
  • Table 2 also lists these results.
  • 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.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Thermal Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Electrochemistry (AREA)
  • Shaping Metal By Deep-Drawing, Or The Like (AREA)
  • Heat Treatment Of Articles (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)
  • Mounting, Exchange, And Manufacturing Of Dies (AREA)

Abstract

A method of manufacturing a hot press-formed part by hot pressing a coated steel sheet formed with a Zn-Ni plating layer on a surface of a steel sheet includes: heating the coated steel sheet to a temperature range of Ac3 transformation temperature to 1000°C; cooling the coated steel sheet to 550-410°C at a cooling rate of 100°C/s or higher by squeezing the coated steel sheet with a press tool for cooling having flat surfaces configured to contact the coated steel sheet; press forming the coated steel sheet with a tool of press forming to obtain a formed body, the press forming being initiated within 5 seconds after the cooling while the temperature of the coated steel sheet is 550-400°C; and quenching the formed body, while squeezing the formed body with the tool of press forming and holding at its press bottom dead center, to obtain a hot press-formed part.

Description

    TECHNICAL FIELD
  • This disclosure relates to a hot press-formed part and a method of manufacturing the same, 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.
    This disclosure also relates to a hot press-formed part produced by the method of manufacturing a hot press-formed part.
  • BACKGROUND
  • 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 (PTL 1) 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.
  • However, the technique proposed in PTL I 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 in PTL 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) 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.
  • 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) 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 Acl 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.
  • CITATION LIST Patent Literature
    • PTL 1 : GB1490535A
    • PTL 2: JP3663145B
    • PTL 3: JP201391099A
    SUMMARY (Technical Problem)
  • 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 in PTL 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.
  • (Solution to Problem)
  • 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. We thus provide the following.
    1. [1] A method of manufacturing a hot press-formed part by hot pressing a coated steel sheet formed with a Zn-Ni plating layer on a surface of a steel sheet, the method comprising: heating the coated steel sheet 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 with a press tool for cooling having flat surfaces configured to contact the coated steel sheet; press forming the coated steel sheet with a tool of press forming to obtain a formed body, the press forming being initiated within 5 seconds after the cooling while the temperature of the coated steel sheet is 550 °C or lower and 400 °C or higher; and quenching the formed body, while squeezing the formed body with the tool of press forming and holding at its press bottom dead center, to obtain a hot press-formed part.
    2. [2] The method of manufacturing a hot press-formed part according to [1], wherein the Zn-Ni plating layer of the coated steel sheet contains 9 mass% or more and 25 mass% or less of Ni.
    3. [3] A hot press-formed part manufactured by the method as recited in [1] or [2].
    (Advantageous Effect)
  • According to the disclosure, 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.
  • BRIEF DESCRIPTION OF THE DRAWING
  • In the accompanying drawings:
    • 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 of FIG. 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.
    DETAILED DESCRIPTION
  • 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 in FIG. 1, comprises: heating (not shown) the coated steel sheet 1 to a temperature range of Ac3 transformation temperature to 1000 °C; cooling (S1) the heated coated steel sheet 1 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 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.
  • <Material of hot press-formed part>
  • 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.
  • <Heating>
  • The coated steel sheet I is heated to a temperature range of Ac3 transformation temperature to 1000 °C. If the heating temperature of the coated steel sheet 1 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 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 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 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.
  • <Cooling>
  • 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 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.
  • In general, when squeezing the heated coated steel sheet I with the press tool for cooling 3, 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. However, 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. 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 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. 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.
    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 I 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 (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 mmφ 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. 5, with emphasis on the horizontal axis, and focusing on an area enclosed by a dashed line in FIG. 5. It can be seen from FIG. 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).
  • 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.
  • 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 in FIG. 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.
  • <Press forming
  • In the press forming (S2), the coated steel sheet I 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'.
  • 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 coated steel sheet 1 from the press tool for cooling 3, and starting press forming while the temperature of the coated steel 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 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. From the perspective of suppressing micro-cracks, crash forming is preferred because of less excessive forming of wall portions of the press formed part.
  • <Quenching>
  • 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: 0.15 % or more and 0.50 % or less>>
  • 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: 0.05 % or more and 2.00 % 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: 0.50 % or more and 3.00 % 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.
  • <<P: 0.10 % 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: 0.050 % or less>>
  • 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.
  • <<A1: 0.10 % or less>>
  • When the A1 content exceeds 0.10 %, oxide inclusions in steel increase, and the ductility of steel decreases. Accordingly, the A1 content is preferably 0.10 % or less, and more preferably 0.07 % or less. A1 functions as a deoxidation material, however, and from the perspective of improving the cleanliness factor of steel, the A1 content is preferably 0.01 % or more.
  • <<N: 0.010 % or less>>
  • 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: 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, and Ni:
    • 0.01 % or more and 0.50 % or less
    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: 0.01 % or more and 0.20 % 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: 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. 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: 0.0002 % or more and 0.0050 % 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: 0.003 % or more and 0.030 % 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 coated steel 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.
  • EXAMPLES
  • 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] 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 Pltysical Metallurgy of Steels", translation supervised by Nariyasu Kouda, translated by Hiroshi Kumai and Talsuhiko Noda, Maruzen Co., Ltd., 1985, p. 273). Ac 3 °C = 910 203 C 0.5 + 44.7 × Si 30 × Mn + 700 × P + 400 × Al
    Figure imgb0001
    Where [C], [Si], [Mn], [P], and [Al] are the contents (in mass%) of the elements enclosed in brackets (C, Si, Mn, P, and Al) in steel.
    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 a coated steel sheet I. Each plating layer was formed under the following conditions.
  • <Pure Zn plating layer>
  • 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.
  • <Zn-Fe plating layer>
  • 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.
  • <Zn-Ni plating layer>
  • 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 a plating layer 23 and a steel sheet 25 toward the center in the thickness direction (as indicated by length h in FIG. 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 in FIG. 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.
    Figure imgb0002
    Figure imgb0003
  • 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.
  • REFERENCE SIGNS LIST
  • 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 (3)

  1. A method of manufacturing a hot press-formed part by hot pressing a coated steel sheet formed with a Zn-Ni plating layer on a surface of a steel sheet, the method comprising:
    heating the coated steel sheet 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 with a press tool for cooling having flat surfaces configured to contact the coated steel sheet;
    press forming the coated steel sheet with a tool of press forming to obtain a formed body, the press forming being initiated within 5 seconds after the cooling while the temperature of the coated steel sheet is 550 °C or lower and 400 °C or higher; and
    quenching the formed body, while squeezing the formed body with the tool of press forming and holding at its press bottom dead center, to obtain a hot press-formed part.
  2. The method of manufacturing a hot press-formed part according to claim 1, wherein the Zn-Ni plating layer of the coated steel sheet contains 9 mass% or more and 25 mass% or less of Ni.
  3. A hot press-formed part manufactured by the method as recited in claim 1 or 2.
EP15843885.3A 2014-09-25 2015-09-07 Method of manufacturing hot press-formed part, and hot press-formed part Active EP3199257B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
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

Publications (3)

Publication Number Publication Date
EP3199257A1 true EP3199257A1 (en) 2017-08-02
EP3199257A4 EP3199257A4 (en) 2017-12-06
EP3199257B1 EP3199257B1 (en) 2021-02-24

Family

ID=55580609

Family Applications (1)

Application Number Title Priority Date Filing Date
EP15843885.3A Active EP3199257B1 (en) 2014-09-25 2015-09-07 Method of manufacturing hot press-formed part, and hot press-formed part

Country Status (7)

Country Link
US (1) US20170225215A1 (en)
EP (1) EP3199257B1 (en)
JP (1) JP6152836B2 (en)
KR (1) KR20170036086A (en)
CN (1) CN106714996B (en)
MX (1) MX2017003875A (en)
WO (1) WO2016047058A1 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6614160B2 (en) * 2014-12-25 2019-12-04 日本製鉄株式会社 Manufacturing method of panel-shaped molded product
US20210114074A1 (en) * 2018-04-13 2021-04-22 Nippon Steel Corporation Production method for hot press molded articles, press molded article, die mold, and mold set
JP6825747B2 (en) * 2019-01-31 2021-02-03 Jfeスチール株式会社 Hot-pressed members, cold-rolled steel sheets for hot-pressed members, and their manufacturing methods
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

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE435527B (en) * 1973-11-06 1984-10-01 Plannja Ab PROCEDURE FOR PREPARING A PART OF Hardened Steel
GB1465209A (en) * 1973-12-17 1977-02-23 Upjohn Co Clindamycin2-phosphates
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
JP3816937B1 (en) * 2005-03-31 2006-08-30 株式会社神戸製鋼所 Steel sheet for hot-formed product, method for producing the same, and hot-formed product
JP4681492B2 (en) * 2006-04-07 2011-05-11 新日本製鐵株式会社 Steel plate hot pressing method and press-formed product
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
ATE554190T1 (en) * 2009-08-25 2012-05-15 Thyssenkrupp Steel Europe Ag METHOD FOR PRODUCING A STEEL COMPONENT AND STEEL COMPONENT PROVIDED WITH A METALLIC COATING TO PROTECT AGAINST CORROSION
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
DE102011053941B4 (en) * 2011-09-26 2015-11-05 Voestalpine Stahl Gmbh Method for producing hardened components with regions of different hardness and / or ductility
KR20130132566A (en) * 2010-12-24 2013-12-04 뵈스트알파인 스탈 게엠베하 Method for producing hardened structural elements
DE102011053939B4 (en) * 2011-09-26 2015-10-29 Voestalpine Stahl Gmbh Method for producing hardened components
EP2754723A3 (en) * 2011-01-17 2016-08-31 Tata Steel IJmuiden BV Method to produce a hot formed part, and part thus formed
JP5817479B2 (en) * 2011-03-10 2015-11-18 Jfeスチール株式会社 Manufacturing method of hot press member
US20140065007A1 (en) * 2011-06-10 2014-03-06 Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) Hot press-formed product, process for producing same, and thin steel sheet for hot press forming
WO2013031984A1 (en) * 2011-09-01 2013-03-07 株式会社神戸製鋼所 Hot-stamp molded part and method for manufacturing same
JP2013075329A (en) * 2011-09-30 2013-04-25 Kobe Steel Ltd Method for manufacturing press-molded article and press molding equipment
WO2013132821A1 (en) * 2012-03-06 2013-09-12 Jfeスチール株式会社 Warm press forming method and automobile frame component
JP5825413B1 (en) * 2014-04-23 2015-12-02 Jfeスチール株式会社 Manufacturing method of hot press-formed product

Also Published As

Publication number Publication date
KR20170036086A (en) 2017-03-31
EP3199257B1 (en) 2021-02-24
WO2016047058A1 (en) 2016-03-31
MX2017003875A (en) 2017-06-08
US20170225215A1 (en) 2017-08-10
CN106714996B (en) 2019-07-05
JP6152836B2 (en) 2017-06-28
CN106714996A (en) 2017-05-24
JP2016064440A (en) 2016-04-28
WO2016047058A8 (en) 2017-01-19
EP3199257A4 (en) 2017-12-06

Similar Documents

Publication Publication Date Title
EP3135394B1 (en) Method for manufacturing hot press forming part
EP2757169B1 (en) High-strength steel sheet having excellent workability and method for producing same
EP3178955B1 (en) High-strength steel sheet and production method for same, and production method for high-strength galvanized steel sheet
EP3178949B1 (en) High-strength steel sheet and method for manufacturing same
EP3050989B1 (en) High-strength steel sheet and method for producing same
EP3199257B1 (en) Method of manufacturing hot press-formed part, and hot press-formed part
EP3040133B1 (en) Method of manufacturing hot press formed part, and hot press formed part
EP3216887B1 (en) Hot-dip galvanized steel sheet
EP3216886A1 (en) Hot-dip galvanized steel sheet
KR101379973B1 (en) High-strength hot-dip galvanized steel sheet and manufacturing method therefor
EP2730672B1 (en) Cold-rolled steel sheet
EP2634281A1 (en) High-strength hot-dip galvanized steel sheet having excellent uniform elongation and plating properties, and method for manufacturing same
CN110121568A (en) High strength galvanized steel plate and its manufacturing method
CN107075643A (en) High-strength steel sheet, high-strength hot-dip zinc-coated steel sheet, high-strength hot aludip and high intensity plated steel sheet and their manufacture method
EP3178956A1 (en) High-strength steel sheet and production method for same, and production method for high-strength galvanized steel sheet
CN108138282A (en) The manufacturing method of hot pressing galvanized steel plain sheet and hot forming product
EP3178957A1 (en) High-strength steel sheet and production method for same, and production method for high-strength galvanized steel sheet
EP3216891A1 (en) Hot-dip galvanized steel sheet
EP3178953A1 (en) High-strength steel sheet and production method for same, and production method for high-strength galvanized steel sheet
KR20140117584A (en) Steel sheet, plated steel sheet, method for producing steel sheet, and method for producing plated steel sheet
KR20190073469A (en) High strength steel sheet and manufacturing method thereof
EP3705592A1 (en) High-strength cold-rolled steel sheet, high-strength plated steel sheet, and production methods therefor
EP3178961B1 (en) High-strength hot-dip-galvanized steel sheet
EP3178960B1 (en) High-strength hot-dip-galvanized steel sheet
JP5708320B2 (en) Cold rolled steel sheet

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20170421

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

A4 Supplementary search report drawn up and despatched

Effective date: 20171108

RIC1 Information provided on ipc code assigned before grant

Ipc: C23C 30/00 20060101ALI20171102BHEP

Ipc: B21D 22/20 20060101AFI20171102BHEP

Ipc: B21D 24/00 20060101ALI20171102BHEP

Ipc: C25D 5/26 20060101ALI20171102BHEP

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20191213

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20201103

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1363809

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210315

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602015066141

Country of ref document: DE

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20210224

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210525

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210524

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210524

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210624

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1363809

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210224

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210624

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20210924

Year of fee payment: 7

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602015066141

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20210928

Year of fee payment: 7

Ref country code: GB

Payment date: 20210925

Year of fee payment: 7

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

26N No opposition filed

Effective date: 20211125

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20210930

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210624

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210907

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210907

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210930

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210930

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20210930

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602015066141

Country of ref document: DE

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20220907

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20150907

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220930

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230401

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220907

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210224