EP2733228A1 - Hot press forming steel plate, formed member using same, and method for manufacturing the plate and member - Google Patents

Hot press forming steel plate, formed member using same, and method for manufacturing the plate and member Download PDF

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Publication number
EP2733228A1
EP2733228A1 EP11869574.1A EP11869574A EP2733228A1 EP 2733228 A1 EP2733228 A1 EP 2733228A1 EP 11869574 A EP11869574 A EP 11869574A EP 2733228 A1 EP2733228 A1 EP 2733228A1
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EP
European Patent Office
Prior art keywords
steel sheet
less
hot
excluding
temperature
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
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EP11869574.1A
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German (de)
French (fr)
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EP2733228B1 (en
EP2733228A4 (en
Inventor
Kyoo-Young Lee
Jin-Keun Oh
Jong-Sang Kim
Tae-Kyo HAN
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Posco Holdings Inc
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Posco Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/38Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21BROLLING OF METAL
    • B21B1/00Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations
    • B21B1/02Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations for rolling heavy work, e.g. ingots, slabs, blooms, or billets, in which the cross-sectional form is unimportant ; Rolling combined with forging or pressing
    • B21B1/026Rolling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21CMANUFACTURE OF METAL SHEETS, WIRE, RODS, TUBES OR PROFILES, OTHERWISE THAN BY ROLLING; AUXILIARY OPERATIONS USED IN CONNECTION WITH METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL
    • B21C47/00Winding-up, coiling or winding-off metal wire, metal band or other flexible metal material characterised by features relevant to metal processing only
    • B21C47/26Special arrangements with regard to simultaneous or subsequent treatment of the material
    • 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0263Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment following hot rolling
    • 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
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/001Ferrous alloys, e.g. steel alloys containing N
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    • 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
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
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    • 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
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
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    • C22C38/08Ferrous alloys, e.g. steel alloys containing nickel
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/12Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
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    • C22C38/14Ferrous alloys, e.g. steel alloys containing titanium or zirconium
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    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
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    • C22C38/00Ferrous alloys, e.g. steel alloys
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    • C22C38/22Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
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    • C22C38/00Ferrous alloys, e.g. steel alloys
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    • C22C38/28Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
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    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/32Ferrous alloys, e.g. steel alloys containing chromium with boron
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/34Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of silicon
    • 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
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/12Aluminium or alloys based thereon
    • 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/001Austenite
    • 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/002Bainite
    • 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226Hot rolling
    • 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0236Cold rolling
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    • 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0273Final recrystallisation annealing
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12736Al-base component
    • Y10T428/1275Next to Group VIII or IB metal-base component
    • Y10T428/12757Fe
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12771Transition metal-base component
    • Y10T428/12785Group IIB metal-base component
    • Y10T428/12792Zn-base component
    • Y10T428/12799Next to Fe-base component [e.g., galvanized]

Definitions

  • the present disclosure relates to a steel sheet for hot press forming, a member formed using the steel sheet, and methods for manufacturing the steel sheet and the member, and more particularly, to a steel sheet for manufacturing high-strength and high-ductility products suitable for impact members and crashworthy members of automobiles through a hot press forming process, a member formed using the steel sheet, and methods of manufacturing the steel sheet and the member.
  • AHSS high strength steel
  • DP dual phase
  • TRIP transformation induced plasticity
  • Such steel sheets have a tensile strength of about 500 MPa to 1,000 MPa which may be insufficient to satisfy current rigidity and crash safety requirements while allowing for the lightening of automobiles.
  • hot press forming has been commercialized to overcome such limitations and realize ultra high-strength automotive components.
  • a steel sheet is subjected to heating to an Ac 3 temperature or higher for transformation into austenite, extracting, press forming, and die quenching, so as to form a martensite or mixed martensite-bainite microstructure.
  • Ultra high-strength members having a tensile strength of 1 GPa or greater and high dimensional precision owning to high-temperature forming can be obtained using the hot press forming method.
  • a hot press forming method of the related art is suitable for satisfying rigidity and crash safety requirements while lightening automotive components, final products have an elongation of 10% or less. That is, final products have a very low level of ductility.
  • components manufactured by a hot press forming method may be used as impact members in automobiles, but may not be suitable for use as crashworthy members that absorb crash energy to protect vehicle occupants in a crash.
  • aspects of the present disclosure may provide a steel sheet for manufacturing a hot-press formed member having high strength and high ductility, a member formed using the steel sheet, and methods for manufacturing the steel sheet and the member.
  • a steel sheet for hot press forming may include, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities.
  • a method for manufacturing a steel sheet for hot press forming may include: heating a steel slab to a temperature within a range of 1100°C to 1300°C, the steel slab including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, A1: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; performing a finish hot-rolling process at a temperature within a range of an Ar 3 transformation point to 950°C to form a steel sheet; and coiling the steel sheet at a temperature within a range of M s to 720°C.
  • a hot-press formed member may include, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities, wherein the hot-press formed member has a dual phase microstructure formed by bainite and retained austenite.
  • a method for manufacturing a hot-press formed member may include: heating a steel sheet to a temperature equal to or higher than Ac 3 , the steel sheet including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; hot-press forming the heated steel sheet; cooling the hot-press formed steel sheet to a temperature within a range of M s to 550°C at a rate of 20°C/sec or higher; and heat-treating the cooled steel sheet at a temperature within a range of M s to 550°C in a heating furnace.
  • the present disclosure provides a high-strength, high-ductility steel sheet for hot press forming.
  • the present disclosure also provides a member formed using the steel sheet and having a dual phase microstructure constituted by bainite and retained austenite and a TS(MPa)*El(%) value of 25,000 MPa% or greater. Since the member has high ductility as well as high strength, the member may be usefully used as a crashworthy member of an automobile.
  • Embodiments of the present disclosure provide a method for manufacturing a formed member having a high degree of ductility as well as high strength for use as a crashworthy member of an automobile, and a steel sheet having a high degree of ductility for use in manufacturing such a formed member.
  • the present disclosure provides four categories: a steel sheet for hot press forming having a high degree of ductility, a method for manufacturing the steel sheet, a hot-press formed member, and a method for manufacturing the hot-press formed member.
  • the steel sheet for hot press forming has a high degree of ductility as well as a high degree of strength so that a member formed of the steel sheet through a hot press forming process may have a high degree of ductility and a high degree of strength.
  • the steel sheet for hot press forming includes, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities.
  • Carbon (C) is an element included in the steel sheet to enhance the strength thereof. Furthermore, in the embodiment of the present disclosure, carbon (C) is diffused into retained austenite by elements such as silicon (Si) to stabilize the retained austenite and thus to prevent transformation to martensite.
  • the steel sheet for hot press forming may include 0.3 wt% to 1.0 wt% of carbon (C). If the carbon content is less than 0.3%, the amount of retained austenite is low after forming, and thus it may be difficult to guarantee both strength and ductility. If the carbon content is greater than 1.0%, bainite transformation is markedly slowed, and the formation of pearlite is facilitated, thereby deteriorating properties of the steel sheet.
  • Manganese (Mn) is included in the steel sheet to prevent red shortness caused by FeS formed by sulfur (S) inevitably included in the steel sheet during a manufacturing process.
  • the content of manganese (M) may be within the range of 0.01% to 4.0%. If the content of manganese (M) is less than 0.01%, red shortness may be caused by FeS. If the content of manganese (M) is greater than 4.0%, bainite transformation may be slowed to increase the time required for a heat treatment in a hot press forming process. As a result, the productivity of the hot press forming process may be lowered, and the manufacturing cost of the steel sheet may be increased.
  • Silicon (Si) is an element included in the steel sheet to guarantee the ductility of a final product. Silicon (Si) facilitates ferrite transformation and diffuses carbon (C) into retained austenite to stabilize the retained austenite by an increased amount of carbon (C) in the retained austenite, thereby preventing transformation to martensite.
  • the content of silicon (Si) may be within the range of 1.0 wt% to 2.0 wt%. If the content of silicon (Si) is less than 1.0%, the effect of stabilizing retained austenite may be poor. If the content of silicon (Si) is greater than 2.0%, the rolling characteristics of the steel sheet may be deteriorated. For example, the steel sheet may be cracked during a rolling process. Therefore, the upper limit of the content of silicon (Si) is set as 2.0%.
  • Aluminum (Al) removes oxygen from the steel sheet to prevent the inclusion of nonmetallic substances therein during solidification.
  • aluminum (Al) facilitates the diffusion of carbon (C) into retained austenite to stabilize the retained austenite.
  • the content of aluminum (Al) may be within the range of 0.01% to 2.0%. If the content of aluminum (Al) is less than 0.01%, oxygen may be insufficiently removed, and thus it may be difficult to prevent the inclusion of nonmetallic substances. If the content of aluminum (Al) is greater than 2.0%, the unit cost of steel making may be increased.
  • Sulfur (S) is an element inevitably included in the steel sheet during a manufacturing process thereof. Sulfur (S) combines with iron (Fe) to form FeS causing red shortness. Therefore, it may be necessary to keep the content of sulfur (S) as low as possible. For example, the content of sulfur (S) may be limited to 0.015% or less.
  • Nitrogen (N) is an element inevitably included in the steel sheet during a manufacturing process. The content of nitrogen (N) may be kept as low as possible. For example, the content of nitrogen (N) may be limited to 0.01% or less.
  • the steel sheet for hot press forming may further include at least one element selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  • Molybdenum (Mo) may be added to the steel sheet to suppress the formation of pearlite. Since molybdenum (Mo) is relatively expensive and may increase the manufacturing cost of the steel sheet, 0.5 wt% or less of molybdenum (Mo) may be added.
  • Chromium (Cr) may be added to the steel sheet to suppress the formation of ferrite and expand bainite transformation. If the content of chromium (Cr) is greater than 1.5 wt%, chromium carbide may be formed to lower the amount of dissolved carbon (C). Therefore, 1.5 wt% or less of chromium (Cr) may be added.
  • Nickel (Ni) may be added to increase the faction of austenite and the hardenability of the steel sheet. Since nickel (Ni) is expensive and increases the manufacturing cost of the steel sheet, 0.5 wt% or less of nickel (Ni) may be added.
  • Niobium (Nb) may be added to improve the strength, grain refining characteristics, and ductility of the steel sheet. During reheating, niobium (Nb) suppresses grain growth, and during cooling, niobium (Nb) delays transformation of austenite into ferrite. 0.005 wt% to 0.1 wt% of niobium (Nb) may be added. If the content of niobium (Nb) is less than 0.005%, it is difficult to assure the effect of grain refinement, and if the content of niobium (Nb) is greater than 0.1%, carbonitrides may excessively precipitate to cause delayed fractures in the steel sheet or decrease the workability of the steel sheet.
  • Vanadium (V) may be added to improve the strength, grain refining characteristics, and hardenability of the steel sheet. 0.005 wt% to 0.1 wt% of vanadium (V) may be added. If the content of vanadium (V) is less than 0.005%, such effects may not be obtained, and if the content of vanadium (V) is greater than 0.1%, carbonitrides may excessively precipitate to cause delayed fractures in the steel sheet or decrease the workability of the steel sheet.
  • the steel sheet for hot press forming may further include B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  • Boron (B) may be added to suppress the formation of ferrite. If the content of boron (B) is greater than 0.005 wt%, boron (B) may combine with iron (Fe) or carbon (C) to form a compound facilitating the formation of ferrite. Therefore, 0.005 wt% of less of boron (B) may be added.
  • Titanium (Ti) may be added to maximize the effect of boron (B). Titanium (Ti) combines with nitrogen (N) existing as an impurity in the steel sheet to form TiN, and thus boron (B) may not combine with nitrogen (N). Therefore, the formation of ferrite may be suppressed by boron (B). This effect may be assured by adding 0.06 wt% or less of titanium (Ti).
  • the steel sheet may be a hot-rolled or cold-rolled steel sheet.
  • the steel sheet may be a cold-rolled steel sheet coated with a plating layer for improving corrosion resistance and suppressing the formation of a surface oxide layer.
  • the steel sheet for hot press forming since the steel sheet for hot press forming has high strength and high ductility owing to the above-described composition, the steel sheet may be usefully used to manufacture hot-press formed members (described later) having high strength and ductility.
  • This embodiment is an exemplary example for manufacturing a steel sheet suitable for manufacturing a hot-press formed member having improved ductility.
  • the method for manufacturing a steel sheet for hot press forming includes: heating a steel slab to a temperature within a range of 1100°C to 1300°C, the steel slab including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; performing a finish hot-rolling process at a temperature within a range of Ar 3 transformation point to 950°C to form a steel sheet; and coiling the steel sheet at a temperature within a range of M s to 720°C.
  • the continuous-casting structure of the steel slab may be insufficiently uniformized, and it may be difficult to assure a finish rolling temperature. If the steel slab is heated to a temperature greater than 1300°C, the size of crystal grains and the possibility of surface oxidation may increase to deteriorate the strength and surface properties of the steel slab. Therefore, the steel slab may be heated to a temperature within a range of 1100°C to 1300°C.
  • the finish hot-rolling temperature is lower than Ar 3 transformation point, dual phase rolling may occur to result in hot-rolling mixed grain sizes, and if the finish hot-rolling temperature is higher than 950°C, crystal grains may be coarsened and surface oxidation may occur during the finish hot-rolling process. Therefore, the finish hot-rolling temperature may be within the range of the Ar 3 transformation point to 950°C.
  • the coiling temperature is lower than M s , austenite may transform to martensite to decrease the ductility of the steel sheet and thus to make it difficult to perform a hot coiling process on the steel sheet. If the coiling temperature is higher than 720°C, a thick surface oxide layer may be formed on the steel sheet together with internal oxidation in the steel sheet. Therefore, the coiling temperature may be within the range of M s to 720°C.
  • the method for manufacturing a steel sheet for hot press forming may include: heating a steel slab to a temperature within a range of 1100°C to 1300°C, the steel slab including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; performing a finish hot-rolling process at a temperature within a range of Ar 3 transformation point to 950°C to form a steel sheet; coiling the steel sheet at a temperature within a range of M s to 720°C; pickling the steel sheet; cold-rolling the steel sheet; continuously annealing the steel sheet at a temperature within a range of 750°C to 900°C; and overaging the steel sheet at a temperature within a range of M s to 550°C.
  • the pickling of the steel sheet is performed to remove surface oxides formed during the heating and finish hot-rolling processes. Thereafter, the cold-rolling process is performed. If the continuous annealing temperature for the cold-rolled steel sheet is lower than 750°C, recrystallization may occur insufficiently, and thus a desired degree of workability of the steel sheet may not be obtained. If the continuous annealing temperature is higher than 900°C, it may difficult to heat the steel sheet to the continuous annealing temperature due to the limitation of heating equipment. In addition, if the overaging temperature is lower than M s , martensite may be formed to excessively increase the strength of the steel sheet and negatively affect the ductility of the steel sheet.
  • the overaging temperature is higher than 550°C, the processability of the steel sheet may be lowered due to roll surface deterioration in an annealing furnace, and intended carbide precipitation and bainite transformation may not occur in the overaging process.
  • the method for manufacturing a steel sheet for hot press forming may include: heating a steel slab to a temperature range of 1100°C to 1300°C, the steel slab including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% % to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; performing a finish hot-rolling process at a temperature within a range of Ar 3 transformation point to 950°C to form a steel sheet; coiling the steel sheet at a temperature within a range of M s to 720°C; pickling the steel sheet; cold-rolling the steel sheet; continuously annealing the steel sheet at a temperature within a range of 750°C to 900°C; overaging the steel sheet at a temperature within a range of M s to 550°C; and plating the overaged steel sheet by any one of hot-dip galvanizing, galv
  • a hot-dip galvanized steel sheet may be manufactured by dipping a cold-rolling steel sheet in a galvanizing bath.
  • a galvannealed steel sheet may be manufactured by dipping a cold-rolled steel sheet in a plating bath and performing an alloying heat-treatment process on the steel sheet.
  • An electro-galvanized steel sheet may be manufactured by performing an electro galvanizing process or a Zn-Fe electroplating process on a cold-rolled steel sheet in a continuous electroplating line.
  • a hot-dip aluminized steel sheet may be manufactured by heating a cold-rolled steel sheet, dipping the steel sheet in an aluminum plating bath, and cooling the steel sheet at room temperature at a cooling rate of 5°C/sec to 15°C/sec.
  • the steel slab may further include at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  • the steel slab may further include B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  • the hot-press formed member has high ductility and high strength.
  • the hot-press formed member includes, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities.
  • the hot-press formed member may have a microstructure formed of bainite and retained austenite without martensite.
  • the hot-press formed member may further include at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  • the hot-press formed member may further include B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  • Hot-press formed members of the related art are manufactured to have ultra high strength, and thus martensite is requisitely formed therein.
  • martensite lowers the ductility of such hot-press formed members and thus makes such hot-press formed members unsuitable to be used as crashworthy members of automobiles. Therefore, in the embodiment of the present disclosure, the formation of martensite in the hot-press formed member is suppressed, and the amount of retained austenite is increased.
  • the hot-press formed member has dual phases: bainite and retained austenite.
  • the hot-press formed member having the above-mentioned composition and microstructure has good strength-ductility balance.
  • TS*E1 of the hot-press formed member may be 25,000 or greater so as to be used as a crashworthy member of an automobile as well as being used as an impact member, where TS denotes tensile strength [MPa] and El denotes elongation [%].
  • the method is for performing a hot press forming process on the above-described steel sheet to provide an ultra high-strength automotive component having high ductility.
  • the method includes: heating a steel sheet to a temperature equal to or higher than Ac 3 , the steel sheet including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; hot-press forming the heated steel sheet; cooling the hot-press formed steel sheet to a temperature range of M s to 550°C at a rate of 20°C/sec or higher; and heat-treating the cooled steel sheet in a heating furnace heated at a temperature within a range of M s to 550°C.
  • the steel sheet may further include at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  • the steel sheet may further include B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  • the steel sheet may be one of a hot-rolled steel sheet, a cold-rolled steel sheet, and a plated cold-rolled steel sheet coated with a plating layer.
  • the heat-treating after the hot-press forming is controlled differently as compared with the case of the related art, so as to manufacture a hot-press formed member having a different microstructure for improving ductility as compared with a hot-press formed member of the related art. That is, in the related art, heat-treatment conditions are adjusted to form martensite as a main microstructure to finally obtain an ultra high-strength member.
  • heat treatment conditions for forming a microstructure constituted by bainite and retained austenite without martensite.
  • the steel sheet is heated to a temperature equal to Ac 3 or higher for transformation to austenite, and is then hot-press formed.
  • a hot-press formed steel sheet is directly die-quenched to a temperature equal to or lower than M s so as to form martensite as a main microstructure in a final product and thus to enhance the strength of the final product.
  • martensite is excluded from the microstructure of a final product so as to improve the ductility of the final product while maintaining the strength of the final product at a level suitable for weight reduction.
  • the hot-press formed steel sheet instead of cooling the hot-press formed steel sheet directly to room temperature equal to or lower than M s , the hot-press formed steel sheet is cooled to a temperature range of M s to 550°C, and heat-treated in a heating furnace at a temperature within a range of M s to 550°C so as to cause the hot-press formed steel sheet to undergo transformation to bainite.
  • the cooling rate is adjusted to be within the range of M s to 550°C to form a dual phase microstructure constituted by bainite and retained austenite.
  • Fe 3 C carbide may not be formed because elements such as silicon (Si) are sufficiently included in the steel sheet to diffuse carbon (C) into the retained austenite. That is, carbon (C) does not form carbides but is dissolved in the retained austenite to stabilize the retained austenite and thus to lower M s . Therefore, in the next cooling process, transformation to martensite is suppressed. Therefore, in a final product, the retained austenite remains instead of undergoing transformation to martensite, thereby improving ductility.
  • elements such as silicon (Si) are sufficiently included in the steel sheet to diffuse carbon (C) into the retained austenite. That is, carbon (C) does not form carbides but is dissolved in the retained austenite to stabilize the retained austenite and thus to lower M s . Therefore, in the next cooling process, transformation to martensite is suppressed. Therefore, in a final product, the retained austenite remains instead of undergoing transformation to martensite, thereby improving ductility.
  • the cooling rate may be 20°C/sec or higher. If the cooling rate is lower than 20°C/sec, transformation to pearlite may easily occur to lower properties of a final product.
  • bainite was formed at a cooling rate of 30°C/sec.
  • FIGS. 2B and 2C a pearlite structure in which ferrite and Fe 3 C were layered was formed at a cooling rate of 5°C/sec.
  • the above-described processes for manufacturing a hot-press formed member according to the embodiment of the present disclosure may be summarized as follows. First, a steel sheet is inserted in a heating furnace to heat the steel sheet to Ac 3 or higher for forming austenite, and then the heated steel sheet is hot-press formed. After the hot press forming, the steel sheet is cooled to a temperature range of M s to 550°C at a cooling rate of 20°C/sec or higher so as not to form pearlite, and is then heat-treated in a heating furnace at a temperature within a range of M s to 550°C. These processes are for transformation to bainite, and during the processes, carbon (C) diffuses into austenite to lower M s . Although a hot-press formed member manufactured through the above-described processes is cooled to room temperature without any controlling, transformation to martensite does not occur. That is, a dual phase microstructure constituted by bainite and retained austenite may be obtained.
  • Steel ingots 90 mm in length and 175 mm in width having compositions shown in Table 1 were manufactured by vacuum melting, and were then re-heated at 1200°C for 1 hour. Thereafter, the steel ingots were hot-rolled to obtain steel sheets having a thickness of 3 mm. At that time, a finish hot-rolling temperature was Ar 3 or higher. Then, after cooling the steel sheets, the steel sheets were inserted into a heating furnace previously heated to 600°C and left in the heating furnace for 1 hour. Thereafter, the steel sheets were cooled in the heating furnace to simulate hot coiling. Next, the steel sheets were cold-rolled at a reduction ratio of 60% to a thickness of 1.2 mm and were annealed at 900°C.
  • the 1.2 mm thickness steel sheets manufactured as described above were heated to a temperature of 900°C and maintained at the temperature for 30 seconds. Then, the steel sheets were cooled to cooling temperatures at a rate of 30°C/sec. Next, the steel sheets were inserted into a heating furnace and heat-treated in the heating furnace at the same temperatures as the cooling temperatures for 400 seconds to 10,800 seconds. Thereafter, the steel sheets were air-cooled. In this way, hot-press formed members were obtained.
  • the process conditions and mechanical properties of the hot-press formed members are shown in Table 2 below.
  • Comparative Steel 1 Since TS*E1 of Comparative Steel 1 cooled at a cooling rate of 400°C is 16,785 MPa%, Comparative Steel 1 is not suitable as a crashworthy member of an automobile. The reason for this may be that the insufficient content of carbon (C) led to failure in stabilizing retained austenite. In the case that the cooling rate was 250°C, Comparative Steel 1 was cooled to a temperature lower than M s to result in a large amount of transformation to martensite, and thus Comparative Steel 1 had high strength but low ductility. In this case, TS*El of Comparative Steel 1 is 9,066 MPa%, and Comparative Steel 1 is not suitable to form a crashworthy member of an automobile.
  • Comparative Steel 2 The carbon (C) content and silicon (Si) content of Comparative Steel 2 are also not sufficient to stabilize retained austenite, and the cooling temperature of Comparative Steel 2 is equal to or lower than M s to result in transformation to martensite. Therefore, Comparative Steel 2 has low ductility, and TS*El thereof is low at 10,150 MPa%. Comparative Steel 3 also has an insufficient content of carbon (C), and the cooling temperature of Comparative Steel 3 is equal to or lower than M s . Therefore, TS*El of Comparative Steel 3 is low at 8,940 MPa%, and Comparative Steel 3 is not suitable to form a crashworthy member of an automobile.
  • Comparative Steel 4 has a sufficient content of carbon (C), the silicon (Si) content of Comparative Steel 4 is not sufficient to fully diffuse carbon (C) into retained austenite. Therefore, although TS*El of Comparative Steel 4 is relatively high at 19,216 MPa% as compared with other comparative steels, TS*El of Comparative Steel 4 is not greater than 25,000 MPa%. That is, Comparative Steel 4 is not suitable for forming a crashworthy member of an automobile.
  • Samples of Inventive Steel 7 having a composition within the range of the present disclosure were cooled at a cooling rate of 30°C/sec and at a cooling rate of 5°C/sec, respectively.
  • TS*El of Inventive Steel 7 was high at 46,923 MPa% and suitable for a crashworthy member of an automobile.
  • TS*El of Inventive Steel 7 was low at 12,480 MPa% and not suitable for a crashworthy member of an automobile. The reason for this may be that the low cooling rate led to the formation of pearlite as shown in FIGS. 2A to 2C and deterioration of properties thereof.

Abstract

The present invention relates to a hot press forming steel plate made of a composition comprising: 0.3-1.0 wt % of C; 0.01-4.0 wt % of Mn; 1.0-2.0 wt % of Si; 0.01-2.0 wt % of Al; 0.015 wt % or less of S; 0.01 wt % or less of N; and the remainder being Fe and unavoidable impurities. Further, the present invention relates to a method for manufacturing the hot press forming steel plate, characterized by comprising the steps of: heating, to between 1100 and 1300°C, a steel slab having the composition; performing hot rolling finishing between an Ar3 transformation point and 950°C; and performing winding between MS and 720°C. Further, the present invention relates to a hot press formed member characterized by having the composition, and having a dual phase microstructure made of bainite and residual austenite. In addition, the present invention relates to a method for manufacturing the hot press formed member, characterized by comprising the steps of: heating the steel plate having the composition to a temperature of an Ac3 point or higher; hot press molding the heated steel plate; performing cooling at a cooling speed of 20°C/sec or higher to a temperature between MS and 550°C; and performing a heat treatment in a heating furnace between MS and 550°C.

Description

    [Technical Field]
  • The present disclosure relates to a steel sheet for hot press forming, a member formed using the steel sheet, and methods for manufacturing the steel sheet and the member, and more particularly, to a steel sheet for manufacturing high-strength and high-ductility products suitable for impact members and crashworthy members of automobiles through a hot press forming process, a member formed using the steel sheet, and methods of manufacturing the steel sheet and the member.
  • [Background Art]
  • Recently, safety regulations for protecting automobile occupants and fuel efficiency regulations for protecting the environment have been greatly tightened, and social requirements for vehicle weight reductions have markedly increased. The use of high-strength steel sheets is necessary to reduce the weight of automotive parts while maintaining the rigidity thereof and the crash safety of automobiles.
  • However, if steel sheets for automobiles are improved in strength, the yield strength thereof is inevitably increased, and the elongation thereof is reduced. These factors significantly lower the formability of such steel sheets. In addition, due to excessive spring-back in high-strength steel sheets, the dimensions of components formed of high-strength steel sheets may be varied after a forming process. That is, the shape fixability of components may be lowered.
  • To address these limitations, advanced high strength steel (AHSS), such as dual phase (DP) steel in which martensite is included in a ferrite matrix to lower the yield ratio thereof and transformation induced plasticity (TRIP) steel in which bainite and retained austenite are included in a ferrite matrix to markedly increase the strength-elongation balance thereof, have been developed and commercialized.
  • However, such steel sheets have a tensile strength of about 500 MPa to 1,000 MPa which may be insufficient to satisfy current rigidity and crash safety requirements while allowing for the lightening of automobiles.
  • Therefore, a steel forming method known as hot press forming has been commercialized to overcome such limitations and realize ultra high-strength automotive components. In the hot press forming method, after blanking, a steel sheet is subjected to heating to an Ac3 temperature or higher for transformation into austenite, extracting, press forming, and die quenching, so as to form a martensite or mixed martensite-bainite microstructure. Ultra high-strength members having a tensile strength of 1 GPa or greater and high dimensional precision owning to high-temperature forming can be obtained using the hot press forming method.
  • Although such a hot press forming method of the related art is suitable for satisfying rigidity and crash safety requirements while lightening automotive components, final products have an elongation of 10% or less. That is, final products have a very low level of ductility. In other words, components manufactured by a hot press forming method may be used as impact members in automobiles, but may not be suitable for use as crashworthy members that absorb crash energy to protect vehicle occupants in a crash.
  • Therefore, to use hot-press formed members as crashworthy members of automobiles, research into members having a high degree of ductility after being hot-press formed and steel sheets for forming such members through a hot press forming process is required.
  • [Disclosure] [Technical Problem]
  • Aspects of the present disclosure may provide a steel sheet for manufacturing a hot-press formed member having high strength and high ductility, a member formed using the steel sheet, and methods for manufacturing the steel sheet and the member.
  • [Technical Solution]
  • According to an aspect of the present disclosure, a steel sheet for hot press forming may include, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities.
  • According to another aspect of the present disclosure, a method for manufacturing a steel sheet for hot press forming may include: heating a steel slab to a temperature within a range of 1100°C to 1300°C, the steel slab including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, A1: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; performing a finish hot-rolling process at a temperature within a range of an Ar3 transformation point to 950°C to form a steel sheet; and coiling the steel sheet at a temperature within a range of Ms to 720°C.
  • According to another aspect of the present disclosure, a hot-press formed member may include, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities, wherein the hot-press formed member has a dual phase microstructure formed by bainite and retained austenite.
  • According to another aspect of the present disclosure, a method for manufacturing a hot-press formed member may include: heating a steel sheet to a temperature equal to or higher than Ac3, the steel sheet including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; hot-press forming the heated steel sheet; cooling the hot-press formed steel sheet to a temperature within a range of Ms to 550°C at a rate of 20°C/sec or higher; and heat-treating the cooled steel sheet at a temperature within a range of Ms to 550°C in a heating furnace.
  • [Advantageous Effects]
  • The present disclosure provides a high-strength, high-ductility steel sheet for hot press forming. The present disclosure also provides a member formed using the steel sheet and having a dual phase microstructure constituted by bainite and retained austenite and a TS(MPa)*El(%) value of 25,000 MPa% or greater. Since the member has high ductility as well as high strength, the member may be usefully used as a crashworthy member of an automobile.
  • [Description of Drawings]
    • FIG. 1 is a temperature-time graph illustrating manufacturing processes of a hot-press formed member according to an embodiment of the present disclosure.
    • FIGS. 2A to 2C are images showing microstructures of hot-press formed members according to cooling rates after a forming process in a method for manufacturing a hot-press formed member, in which FIG. 2A is the case of a cooling rate of 30°C/sec, FIG. 2B is the case of a cooling rate of 5°C/sec, and FIG. 2C is an enlarged image of FIG. 2B.
    [Best Mode]
  • Embodiments of the present disclosure provide a method for manufacturing a formed member having a high degree of ductility as well as high strength for use as a crashworthy member of an automobile, and a steel sheet having a high degree of ductility for use in manufacturing such a formed member. In detail, the present disclosure provides four categories: a steel sheet for hot press forming having a high degree of ductility, a method for manufacturing the steel sheet, a hot-press formed member, and a method for manufacturing the hot-press formed member.
  • (Steel sheet for hot press forming)
  • Hereinafter, a steel sheet for hot press forming will be described in detail according to an embodiment of the present disclosure.
  • The steel sheet for hot press forming has a high degree of ductility as well as a high degree of strength so that a member formed of the steel sheet through a hot press forming process may have a high degree of ductility and a high degree of strength. The steel sheet for hot press forming includes, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities.
  • Carbon (C) is an element included in the steel sheet to enhance the strength thereof. Furthermore, in the embodiment of the present disclosure, carbon (C) is diffused into retained austenite by elements such as silicon (Si) to stabilize the retained austenite and thus to prevent transformation to martensite. The steel sheet for hot press forming may include 0.3 wt% to 1.0 wt% of carbon (C). If the carbon content is less than 0.3%, the amount of retained austenite is low after forming, and thus it may be difficult to guarantee both strength and ductility. If the carbon content is greater than 1.0%, bainite transformation is markedly slowed, and the formation of pearlite is facilitated, thereby deteriorating properties of the steel sheet.
  • Manganese (Mn) is included in the steel sheet to prevent red shortness caused by FeS formed by sulfur (S) inevitably included in the steel sheet during a manufacturing process. The content of manganese (M) may be within the range of 0.01% to 4.0%. If the content of manganese (M) is less than 0.01%, red shortness may be caused by FeS. If the content of manganese (M) is greater than 4.0%, bainite transformation may be slowed to increase the time required for a heat treatment in a hot press forming process. As a result, the productivity of the hot press forming process may be lowered, and the manufacturing cost of the steel sheet may be increased.
  • Silicon (Si) is an element included in the steel sheet to guarantee the ductility of a final product. Silicon (Si) facilitates ferrite transformation and diffuses carbon (C) into retained austenite to stabilize the retained austenite by an increased amount of carbon (C) in the retained austenite, thereby preventing transformation to martensite. The content of silicon (Si) may be within the range of 1.0 wt% to 2.0 wt%. If the content of silicon (Si) is less than 1.0%, the effect of stabilizing retained austenite may be poor. If the content of silicon (Si) is greater than 2.0%, the rolling characteristics of the steel sheet may be deteriorated. For example, the steel sheet may be cracked during a rolling process. Therefore, the upper limit of the content of silicon (Si) is set as 2.0%.
  • Aluminum (Al) removes oxygen from the steel sheet to prevent the inclusion of nonmetallic substances therein during solidification. In addition, like silicon (Si), aluminum (Al) facilitates the diffusion of carbon (C) into retained austenite to stabilize the retained austenite. The content of aluminum (Al) may be within the range of 0.01% to 2.0%. If the content of aluminum (Al) is less than 0.01%, oxygen may be insufficiently removed, and thus it may be difficult to prevent the inclusion of nonmetallic substances. If the content of aluminum (Al) is greater than 2.0%, the unit cost of steel making may be increased.
  • Sulfur (S) is an element inevitably included in the steel sheet during a manufacturing process thereof. Sulfur (S) combines with iron (Fe) to form FeS causing red shortness. Therefore, it may be necessary to keep the content of sulfur (S) as low as possible. For example, the content of sulfur (S) may be limited to 0.015% or less. Nitrogen (N) is an element inevitably included in the steel sheet during a manufacturing process. The content of nitrogen (N) may be kept as low as possible. For example, the content of nitrogen (N) may be limited to 0.01% or less.
  • In addition to the above-mentioned elements, the steel sheet for hot press forming may further include at least one element selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  • Molybdenum (Mo) may be added to the steel sheet to suppress the formation of pearlite. Since molybdenum (Mo) is relatively expensive and may increase the manufacturing cost of the steel sheet, 0.5 wt% or less of molybdenum (Mo) may be added.
  • Chromium (Cr) may be added to the steel sheet to suppress the formation of ferrite and expand bainite transformation. If the content of chromium (Cr) is greater than 1.5 wt%, chromium carbide may be formed to lower the amount of dissolved carbon (C). Therefore, 1.5 wt% or less of chromium (Cr) may be added.
  • Nickel (Ni) may be added to increase the faction of austenite and the hardenability of the steel sheet. Since nickel (Ni) is expensive and increases the manufacturing cost of the steel sheet, 0.5 wt% or less of nickel (Ni) may be added.
  • Niobium (Nb) may be added to improve the strength, grain refining characteristics, and ductility of the steel sheet. During reheating, niobium (Nb) suppresses grain growth, and during cooling, niobium (Nb) delays transformation of austenite into ferrite. 0.005 wt% to 0.1 wt% of niobium (Nb) may be added. If the content of niobium (Nb) is less than 0.005%, it is difficult to assure the effect of grain refinement, and if the content of niobium (Nb) is greater than 0.1%, carbonitrides may excessively precipitate to cause delayed fractures in the steel sheet or decrease the workability of the steel sheet.
  • Vanadium (V) may be added to improve the strength, grain refining characteristics, and hardenability of the steel sheet. 0.005 wt% to 0.1 wt% of vanadium (V) may be added. If the content of vanadium (V) is less than 0.005%, such effects may not be obtained, and if the content of vanadium (V) is greater than 0.1%, carbonitrides may excessively precipitate to cause delayed fractures in the steel sheet or decrease the workability of the steel sheet.
  • In addition, the steel sheet for hot press forming may further include B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  • Boron (B) may be added to suppress the formation of ferrite. If the content of boron (B) is greater than 0.005 wt%, boron (B) may combine with iron (Fe) or carbon (C) to form a compound facilitating the formation of ferrite. Therefore, 0.005 wt% of less of boron (B) may be added.
  • Titanium (Ti) may be added to maximize the effect of boron (B). Titanium (Ti) combines with nitrogen (N) existing as an impurity in the steel sheet to form TiN, and thus boron (B) may not combine with nitrogen (N). Therefore, the formation of ferrite may be suppressed by boron (B). This effect may be assured by adding 0.06 wt% or less of titanium (Ti).
  • The steel sheet may be a hot-rolled or cold-rolled steel sheet. For example, the steel sheet may be a cold-rolled steel sheet coated with a plating layer for improving corrosion resistance and suppressing the formation of a surface oxide layer.
  • According to the embodiment of the present disclosure, since the steel sheet for hot press forming has high strength and high ductility owing to the above-described composition, the steel sheet may be usefully used to manufacture hot-press formed members (described later) having high strength and ductility.
  • (Method for manufacturing steel sheet for hot press forming)
  • Hereafter, a method for manufacturing a steel sheet for hot press forming will be described in detail according to an embodiment of the present disclosure. This embodiment is an exemplary example for manufacturing a steel sheet suitable for manufacturing a hot-press formed member having improved ductility.
  • The method for manufacturing a steel sheet for hot press forming includes: heating a steel slab to a temperature within a range of 1100°C to 1300°C, the steel slab including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; performing a finish hot-rolling process at a temperature within a range of Ar3 transformation point to 950°C to form a steel sheet; and coiling the steel sheet at a temperature within a range of Ms to 720°C.
  • If the steel slab is heated to a temperature lower than 1100°C, the continuous-casting structure of the steel slab may be insufficiently uniformized, and it may be difficult to assure a finish rolling temperature. If the steel slab is heated to a temperature greater than 1300°C, the size of crystal grains and the possibility of surface oxidation may increase to deteriorate the strength and surface properties of the steel slab. Therefore, the steel slab may be heated to a temperature within a range of 1100°C to 1300°C. If the finish hot-rolling temperature is lower than Ar3 transformation point, dual phase rolling may occur to result in hot-rolling mixed grain sizes, and if the finish hot-rolling temperature is higher than 950°C, crystal grains may be coarsened and surface oxidation may occur during the finish hot-rolling process. Therefore, the finish hot-rolling temperature may be within the range of the Ar3 transformation point to 950°C. In addition, if the coiling temperature is lower than Ms, austenite may transform to martensite to decrease the ductility of the steel sheet and thus to make it difficult to perform a hot coiling process on the steel sheet. If the coiling temperature is higher than 720°C, a thick surface oxide layer may be formed on the steel sheet together with internal oxidation in the steel sheet. Therefore, the coiling temperature may be within the range of Ms to 720°C.
  • The method for manufacturing a steel sheet for hot press forming may include: heating a steel slab to a temperature within a range of 1100°C to 1300°C, the steel slab including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; performing a finish hot-rolling process at a temperature within a range of Ar3 transformation point to 950°C to form a steel sheet; coiling the steel sheet at a temperature within a range of Ms to 720°C; pickling the steel sheet; cold-rolling the steel sheet; continuously annealing the steel sheet at a temperature within a range of 750°C to 900°C; and overaging the steel sheet at a temperature within a range of Ms to 550°C.
  • The pickling of the steel sheet is performed to remove surface oxides formed during the heating and finish hot-rolling processes. Thereafter, the cold-rolling process is performed. If the continuous annealing temperature for the cold-rolled steel sheet is lower than 750°C, recrystallization may occur insufficiently, and thus a desired degree of workability of the steel sheet may not be obtained. If the continuous annealing temperature is higher than 900°C, it may difficult to heat the steel sheet to the continuous annealing temperature due to the limitation of heating equipment. In addition, if the overaging temperature is lower than Ms, martensite may be formed to excessively increase the strength of the steel sheet and negatively affect the ductility of the steel sheet. Therefore, before a hot press forming process, blanking may not be easily performed. If the overaging temperature is higher than 550°C, the processability of the steel sheet may be lowered due to roll surface deterioration in an annealing furnace, and intended carbide precipitation and bainite transformation may not occur in the overaging process.
  • The method for manufacturing a steel sheet for hot press forming may include: heating a steel slab to a temperature range of 1100°C to 1300°C, the steel slab including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% % to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; performing a finish hot-rolling process at a temperature within a range of Ar3 transformation point to 950°C to form a steel sheet; coiling the steel sheet at a temperature within a range of Ms to 720°C; pickling the steel sheet; cold-rolling the steel sheet; continuously annealing the steel sheet at a temperature within a range of 750°C to 900°C; overaging the steel sheet at a temperature within a range of Ms to 550°C; and plating the overaged steel sheet by any one of hot-dip galvanizing, galvannealing, electro galvanizing, and hot-dip aluminizing.
  • A hot-dip galvanized steel sheet may be manufactured by dipping a cold-rolling steel sheet in a galvanizing bath. A galvannealed steel sheet may be manufactured by dipping a cold-rolled steel sheet in a plating bath and performing an alloying heat-treatment process on the steel sheet. An electro-galvanized steel sheet may be manufactured by performing an electro galvanizing process or a Zn-Fe electroplating process on a cold-rolled steel sheet in a continuous electroplating line. A hot-dip aluminized steel sheet may be manufactured by heating a cold-rolled steel sheet, dipping the steel sheet in an aluminum plating bath, and cooling the steel sheet at room temperature at a cooling rate of 5°C/sec to 15°C/sec.
  • The steel slab may further include at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%. In addition, the steel slab may further include B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  • (Hot-press formed member)
  • Hereinafter, a hot-press formed member will be described in detail according to an embodiment of the present disclosure.
  • The hot-press formed member has high ductility and high strength. For this, the hot-press formed member includes, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities. The hot-press formed member may have a microstructure formed of bainite and retained austenite without martensite.
  • The hot-press formed member may further include at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%. In addition, the hot-press formed member may further include B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  • Hot-press formed members of the related art are manufactured to have ultra high strength, and thus martensite is requisitely formed therein. However, martensite lowers the ductility of such hot-press formed members and thus makes such hot-press formed members unsuitable to be used as crashworthy members of automobiles. Therefore, in the embodiment of the present disclosure, the formation of martensite in the hot-press formed member is suppressed, and the amount of retained austenite is increased. Thus, the hot-press formed member has dual phases: bainite and retained austenite.
  • The hot-press formed member having the above-mentioned composition and microstructure has good strength-ductility balance. For example, TS*E1 of the hot-press formed member may be 25,000 or greater so as to be used as a crashworthy member of an automobile as well as being used as an impact member, where TS denotes tensile strength [MPa] and El denotes elongation [%].
  • (Method for manufacturing hot-press formed member)
  • Hereinafter, a method for manufacturing a hot-press formed member will be described in detail according to an embodiment of the present disclosure.
  • The method is for performing a hot press forming process on the above-described steel sheet to provide an ultra high-strength automotive component having high ductility. For this, the method includes: heating a steel sheet to a temperature equal to or higher than Ac3, the steel sheet including, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities; hot-press forming the heated steel sheet; cooling the hot-press formed steel sheet to a temperature range of Ms to 550°C at a rate of 20°C/sec or higher; and heat-treating the cooled steel sheet in a heating furnace heated at a temperature within a range of Ms to 550°C.
  • The steel sheet may further include at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%. In addition, the steel sheet may further include B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%). The steel sheet may be one of a hot-rolled steel sheet, a cold-rolled steel sheet, and a plated cold-rolled steel sheet coated with a plating layer.
  • In the method for manufacturing a hot-press formed member according to the embodiment of the present disclosure, the heat-treating after the hot-press forming is controlled differently as compared with the case of the related art, so as to manufacture a hot-press formed member having a different microstructure for improving ductility as compared with a hot-press formed member of the related art. That is, in the related art, heat-treatment conditions are adjusted to form martensite as a main microstructure to finally obtain an ultra high-strength member. However, since such a technique of the related art is not suitable to manufacture a highly ductile member usable as a crashworthy member of an automobile, the inventors have suggested heat treatment conditions for forming a microstructure constituted by bainite and retained austenite without martensite.
  • First, the steel sheet is heated to a temperature equal to Ac3 or higher for transformation to austenite, and is then hot-press formed.
  • The heat-treatment conditions after the hot-press forming have a major effect on determining the microstructure of a product. In the related art, generally, a hot-press formed steel sheet is directly die-quenched to a temperature equal to or lower than Ms so as to form martensite as a main microstructure in a final product and thus to enhance the strength of the final product.
  • However, in the embodiment of the present disclosure, martensite is excluded from the microstructure of a final product so as to improve the ductility of the final product while maintaining the strength of the final product at a level suitable for weight reduction. To this end, instead of cooling the hot-press formed steel sheet directly to room temperature equal to or lower than Ms, the hot-press formed steel sheet is cooled to a temperature range of Ms to 550°C, and heat-treated in a heating furnace at a temperature within a range of Ms to 550°C so as to cause the hot-press formed steel sheet to undergo transformation to bainite. If the steel sheet is cooled to a temperature equal to or lower than Ms, martensite may be formed to lower the ductility of the steel sheet, and if the steel sheet is cooled to a temperature higher than 550°C, pearlite may be formed to deteriorate properties of the steel sheet. Therefore, the cooling rate is adjusted to be within the range of Ms to 550°C to form a dual phase microstructure constituted by bainite and retained austenite.
  • In the bainite formed as described above, Fe3C carbide may not be formed because elements such as silicon (Si) are sufficiently included in the steel sheet to diffuse carbon (C) into the retained austenite. That is, carbon (C) does not form carbides but is dissolved in the retained austenite to stabilize the retained austenite and thus to lower Ms. Therefore, in the next cooling process, transformation to martensite is suppressed. Therefore, in a final product, the retained austenite remains instead of undergoing transformation to martensite, thereby improving ductility.
  • The cooling rate may be 20°C/sec or higher. If the cooling rate is lower than 20°C/sec, transformation to pearlite may easily occur to lower properties of a final product. Referring to FIG. 2A, bainite was formed at a cooling rate of 30°C/sec. However, referring to FIGS. 2B and 2C, a pearlite structure in which ferrite and Fe3C were layered was formed at a cooling rate of 5°C/sec.
  • For example, the above-described processes for manufacturing a hot-press formed member according to the embodiment of the present disclosure may be summarized as follows. First, a steel sheet is inserted in a heating furnace to heat the steel sheet to Ac3 or higher for forming austenite, and then the heated steel sheet is hot-press formed. After the hot press forming, the steel sheet is cooled to a temperature range of Ms to 550°C at a cooling rate of 20°C/sec or higher so as not to form pearlite, and is then heat-treated in a heating furnace at a temperature within a range of Ms to 550°C. These processes are for transformation to bainite, and during the processes, carbon (C) diffuses into austenite to lower Ms. Although a hot-press formed member manufactured through the above-described processes is cooled to room temperature without any controlling, transformation to martensite does not occur. That is, a dual phase microstructure constituted by bainite and retained austenite may be obtained.
  • Hereinafter, the embodiments of the present disclosure will be described more specifically according to examples. The following examples are merely provided to allow for a clear understanding of the present disclosure, rather than to limit the scope thereof.
  • [Mode for Invention] (Examples)
  • Steel ingots 90 mm in length and 175 mm in width having compositions shown in Table 1 were manufactured by vacuum melting, and were then re-heated at 1200°C for 1 hour. Thereafter, the steel ingots were hot-rolled to obtain steel sheets having a thickness of 3 mm. At that time, a finish hot-rolling temperature was Ar3 or higher. Then, after cooling the steel sheets, the steel sheets were inserted into a heating furnace previously heated to 600°C and left in the heating furnace for 1 hour. Thereafter, the steel sheets were cooled in the heating furnace to simulate hot coiling. Next, the steel sheets were cold-rolled at a reduction ratio of 60% to a thickness of 1.2 mm and were annealed at 900°C. Then, the steel sheets were allowed to undergo bainite transformation at 400°C. In Table 1, the contents of elements are given in wt% except for the contents of sulfur (S) and nitrogen (N) given in ppm. [Table 1]
    Steels C Si Mn Al Mo Cr Ni Ti B Nb V S N
    IS* 1 0.40 1.51 3.01 0.04 30 20
    IS 2 0.63 1.49 0.72 0.50 20 20
    IS 3 0.61 1.52 0.63 0.51 0.30 30 20
    IS 4 0.61 1.50 0.65 0.50 0.015 30 20
    IS 5 0.62 1.49 1.61 1.53 0.02 30 20
    IS 6 0.60 1.50 2.91 0.04 0.25 1.20 20 20
    IS 7 0.71 1.47 0.70 0.52 0.010 0.002 20 20
    IS 8 0.68 1.48 0.71 0.04 0.24 30 20
    IS 9 0.70 1.15 0.72 0.51 0.24 30 20
    IS 10 0.71 1.15 0.71 0.04 0.24 0.010 0.002 30 20
    IS 11 0.69 1.55 0.18 0.04 0.24 0.50 0.010 0.002 30 20
    IS 12 0.82 1.49 0.51 0.54 30 20
    IS 13 0.82 1.51 1.01 0.53 30 20
    CS** 1 0.23 1.5 1.5 0.04 30 20
    CS 2 0.20 0.5 1.5 0.03 30 20
    CS 3 0.22 1.5 2 0.03 0.20 20 20
    CS 4 0.68 0.42 0.70 0.52 20 20
    *IS: Inventive Steel, **CS: Comparative Steel
  • To simulate a heat treatment in a heating furnace during a hot press forming process, the 1.2 mm thickness steel sheets manufactured as described above were heated to a temperature of 900°C and maintained at the temperature for 30 seconds. Then, the steel sheets were cooled to cooling temperatures at a rate of 30°C/sec. Next, the steel sheets were inserted into a heating furnace and heat-treated in the heating furnace at the same temperatures as the cooling temperatures for 400 seconds to 10,800 seconds. Thereafter, the steel sheets were air-cooled. In this way, hot-press formed members were obtained. The process conditions and mechanical properties of the hot-press formed members are shown in Table 2 below. [Table 2]
    Steels Cooling Rate (°C/sec) Cooling Temperature (°C) Time (sec) YS (MPa) TS (MPa) El (%) TS*E1 (MPa%) Ms (°C)
    Is* 1 30 400 3600 732 1265 28 35420 295
    IS 2 30 400 3600 899 1187 39 46244 298
    IS 3 30 400 3600 869 1196 37 44252 302
    IS 4 30 400 3600 915 1289 35 45115 307
    IS 5 30 400 3600 883 1185 36 42660 272
    IS 6 30 400 10800 856 1420 26 36920 199
    30 300 10800 985 1610 22 35420 199
    IS 7 30 400 3600 900 1185 40 46923 273
    5 400 3600 719 1128 11 12408 273
    IS 8 30 400 600 816 1310 21 27510 280
    IS 9 30 400 600 915 1240 29 35960 277
    IS 10 30 400 600 845 1318 25 32950 270
    IS 11 30 400 600 940 1288 26 33488 280
    IS 12 30 400 3600 881 1229 35 43556 245
    IS 13 30 400 3600 725 1306 39 50934 228
    CS** 1 30 400 3600 640 1125 15 16875 399
    30 250 3600 1295 1511 6 9066 399
    CS 2 30 250 3600 1220 1450 7 10150 420
    CS 3 30 250 3600 1280 1490 6 8940 384
    CS 4 30 400 3600 870 1201 16 19216 295
    *IS: Inventive Steel, **CS: Comparative Steel
  • Since TS*E1 of Comparative Steel 1 cooled at a cooling rate of 400°C is 16,785 MPa%, Comparative Steel 1 is not suitable as a crashworthy member of an automobile. The reason for this may be that the insufficient content of carbon (C) led to failure in stabilizing retained austenite. In the case that the cooling rate was 250°C, Comparative Steel 1 was cooled to a temperature lower than Ms to result in a large amount of transformation to martensite, and thus Comparative Steel 1 had high strength but low ductility. In this case, TS*El of Comparative Steel 1 is 9,066 MPa%, and Comparative Steel 1 is not suitable to form a crashworthy member of an automobile.
  • The carbon (C) content and silicon (Si) content of Comparative Steel 2 are also not sufficient to stabilize retained austenite, and the cooling temperature of Comparative Steel 2 is equal to or lower than Ms to result in transformation to martensite. Therefore, Comparative Steel 2 has low ductility, and TS*El thereof is low at 10,150 MPa%. Comparative Steel 3 also has an insufficient content of carbon (C), and the cooling temperature of Comparative Steel 3 is equal to or lower than Ms. Therefore, TS*El of Comparative Steel 3 is low at 8,940 MPa%, and Comparative Steel 3 is not suitable to form a crashworthy member of an automobile.
  • Although Comparative Steel 4 has a sufficient content of carbon (C), the silicon (Si) content of Comparative Steel 4 is not sufficient to fully diffuse carbon (C) into retained austenite. Therefore, although TS*El of Comparative Steel 4 is relatively high at 19,216 MPa% as compared with other comparative steels, TS*El of Comparative Steel 4 is not greater than 25,000 MPa%. That is, Comparative Steel 4 is not suitable for forming a crashworthy member of an automobile.
  • Samples of Inventive Steel 7 having a composition within the range of the present disclosure were cooled at a cooling rate of 30°C/sec and at a cooling rate of 5°C/sec, respectively. In the case that the cooling rate was 30°C/sec, TS*El of Inventive Steel 7 was high at 46,923 MPa% and suitable for a crashworthy member of an automobile. However, in the case that the cooling rate was 5°C/sec, TS*El of Inventive Steel 7 was low at 12,480 MPa% and not suitable for a crashworthy member of an automobile. The reason for this may be that the low cooling rate led to the formation of pearlite as shown in FIGS. 2A to 2C and deterioration of properties thereof.

Claims (22)

  1. A steel sheet for hot press forming, comprising, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities.
  2. The steel sheet for hot press forming of claim 1, further comprising at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  3. The steel sheet for hot press forming of claim 1 or 2, further comprising B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  4. The steel sheet for hot press forming of claim 1 or 2, wherein the steel sheet is one of a hot-rolled steel sheet, a cold-rolled steel sheet, and a plated cold-rolled steel sheet coated with a plating layer.
  5. A method for manufacturing a steel sheet for hot press forming, the method comprising:
    heating a steel slab to a temperature range of 1100°C to 1300°C, the steel slab comprising, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities;
    performing a finish hot-rolling process at a temperature within a range of Ar3 transformation point to 950°C to form a steel sheet; and
    coiling the steel sheet at a temperature within a range of Ms to 720°C.
  6. The method of claim 5, wherein the steel slab further comprises at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  7. The method of claim 5 or 6, wherein the steel slab further comprises B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  8. A method for manufacturing a steel sheet for hot press forming, the method comprising:
    heating a steel slab to a temperature range of 1100°C to 1300°C, the steel slab comprising, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities;
    performing a finish hot-rolling process at a temperature within a range of Ar3 transformation point to 950°C to form a steel sheet;
    coiling the steel sheet at a temperature within a range of Ms to 720°C;
    pickling the steel sheet;
    cold-rolling the steel sheet;
    continuously annealing the steel sheet at a temperature within a range of 750°C to 900°C; and
    overaging the steel sheet at a temperature within a range of Ms to 550°C.
  9. The method of claim 8, wherein the steel slab further comprises at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  10. The method of claim 8 or 9, wherein the steel slab further comprises B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  11. A method for manufacturing a steel sheet for hot press forming, the method comprising:
    heating a steel slab to a temperature range of 1100°C to 1300°C, the steel slab comprising, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities;
    performing a finish hot-rolling process at a temperature within a range of Ar3 transformation point to 950°C to form a steel sheet;
    coiling the steel sheet at a temperature within a range of Ms to 720°C;
    pickling the steel sheet;
    cold-rolling the steel sheet;
    continuously annealing the steel sheet at a temperature within a range of 750°C to 900°C;
    overaging the steel sheet at a temperature within a range of Ms to 550°C; and
    plating the overaged steel sheet by any one of hot-dip galvanizing, galvannealing, electro galvanizing, and hot-dip aluminizing.
  12. The method of claim 11, wherein the steel slab further comprises at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  13. The method of claim 11 or 12, wherein the steel slab further comprises B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  14. A hot-press formed member comprising, by wt%, C: 0.3% to 1.00, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities, wherein the hot-press formed member has a dual phase microstructure formed by bainite and retained austenite.
  15. The hot-press formed member of claim 14, further comprising at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  16. The hot-press formed member of claim 14 or 15, further comprising B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  17. The hot-press formed member of claim 14 or 15, wherein the hot-press formed member has a TS(MPa)*El(%) value of 25,000 MPa% or greater.
  18. The hot-press formed member of claim 16, wherein the hot-press formed member has a TS(MPa)*El(%) value of 25,000 MPa% or greater.
  19. A method for manufacturing a hot-press formed member, the method comprising:
    heating a steel sheet to a temperature equal to or higher than Ac3, the steel sheet comprising, by wt%, C: 0.3% to 1.0%, Mn: 0.01% to 4.0%, Si: 1.0% to 2.0%, Al: 0.01% to 2.0%, S: 0.015% or less, N: 0.01% or less, and the balance of Fe and inevitable impurities;
    hot-press forming the heated steel sheet;
    cooling the hot-press formed steel sheet to a temperature range of Ms to 550°C at a rate of 20°C/sec or higher; and
    heat-treating the cooled steel sheet at a temperature within a range of Ms to 550°C in a heating furnace.
  20. The method of claim 19, wherein the steel sheet further comprises at least one selected from the group consisting of Mo: 0.5% or less (excluding 0%), Cr: 1.5% or less (excluding 0%), Ni: 0.5% or less (excluding 0%), Nb: 0.005% to 0.1%, and V: 0.005% to 0.1%.
  21. The method of claim 19 or 20, wherein the steel sheet further comprises B: 0.005% or less (excluding 0%) and Ti: 0.06% or less (excluding 0%).
  22. The method of claim 19 or 20, wherein the steel sheet is one of a hot-rolled steel sheet, a cold-rolled steel sheet, and a plated cold-rolled steel sheet coated with a plating layer.
EP11869574.1A 2011-07-15 2011-07-15 Hot press formed member and method for manufacturing the member Active EP2733228B1 (en)

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PCT/KR2011/005242 WO2013012103A1 (en) 2011-07-15 2011-07-15 Hot press forming steel plate, formed member using same, and method for manufacturing the plate and member

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EP2733228A4 EP2733228A4 (en) 2015-08-12
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EP4089194A4 (en) * 2020-01-09 2023-07-26 Nippon Steel Corporation Hot stamp molded body

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US20140150930A1 (en) 2014-06-05
EP2733228B1 (en) 2019-06-19
JP2014520961A (en) 2014-08-25
CN103687973B (en) 2016-08-31
WO2013012103A1 (en) 2013-01-24
EP2733228A4 (en) 2015-08-12
CN103687973A (en) 2014-03-26

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