EP4656755A1 - Steel sheet and member, and method for producing said steel sheet and method for producing said member - Google Patents

Steel sheet and member, and method for producing said steel sheet and method for producing said member

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Publication number
EP4656755A1
EP4656755A1 EP23928769.1A EP23928769A EP4656755A1 EP 4656755 A1 EP4656755 A1 EP 4656755A1 EP 23928769 A EP23928769 A EP 23928769A EP 4656755 A1 EP4656755 A1 EP 4656755A1
Authority
EP
European Patent Office
Prior art keywords
less
good
steel sheet
steel
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.)
Pending
Application number
EP23928769.1A
Other languages
German (de)
French (fr)
Inventor
Junya TOBATA
Hideyuki Kimura
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 EP4656755A1 publication Critical patent/EP4656755A1/en
Pending legal-status Critical Current

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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
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
    • 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
    • C21D1/18Hardening; Quenching with or without subsequent tempering
    • C21D1/19Hardening; Quenching with or without subsequent tempering by interrupted 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
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/18Hardening; Quenching with or without subsequent tempering
    • C21D1/25Hardening, combined with annealing between 300 degrees Celsius and 600 degrees Celsius, i.e. heat refining ("Vergüten")
    • 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
    • C21D1/26Methods of annealing
    • 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
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/005Heat treatment of ferrous alloys containing Mn
    • 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 of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties of ferrous metals or ferrous alloys 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 of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0236Cold 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 of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties of ferrous metals or ferrous alloys 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 of ferrous metals or ferrous alloys 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
    • C21D8/00Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0273Final recrystallisation annealing
    • 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
    • C22C38/002Ferrous 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
    • C22C38/005Ferrous alloys, e.g. steel alloys containing rare earths, i.e. Sc, Y, Lanthanides
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/008Ferrous alloys, e.g. steel alloys containing tin
    • 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
    • C22C38/08Ferrous alloys, e.g. steel alloys containing nickel
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/10Ferrous alloys, e.g. steel alloys containing cobalt
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/12Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/14Ferrous alloys, e.g. steel alloys containing titanium or zirconium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/16Ferrous alloys, e.g. steel alloys containing copper
    • 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
    • C22C38/34Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous 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
    • 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
    • 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/005Ferrite
    • 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
    • C21D2211/008Martensite

Definitions

  • the present disclosure relates to a steel sheet, a member using the steel sheet as material, and methods of producing same.
  • steel sheets used as material for automotive parts for example, automobile frame parts such as bumpers, are often required, from the viewpoint of press formability, to have high elongation (hereinafter, also referred to as EL).
  • Patent Literature (PTL) 1 describes:
  • Automotive parts often undergo paint baking.
  • toughness and crash properties of a steel sheet may change significantly before and after paint baking. Therefore, in recent years, steel sheets used as material for automotive parts are also required to have excellent toughness and crash properties after paint baking for further improvement of automobile safety.
  • TS is measured by a tensile test in accordance with JIS Z 2241:2022.
  • High EL means an EL of 10 % or more. Further, EL is measured by a tensile test in accordance with JIS Z 2241:2022.
  • Excellent toughness after paint baking means that a brittle-ductile transition temperature after aging treatment is -40 °C or lower.
  • the aging treatment conditions are a treatment temperature of 170 °C and a treatment time of 20 min.
  • the brittle-ductile transition temperature is measured by the Charpy impact test in accordance with JIS Z 2242:2018.
  • Excellent crash properties after paint baking means that a YR after aging treatment is 0.85 or more, and a fracture stress ratio after aging treatment is 0.90 or less.
  • the aging treatment conditions are a treatment temperature of 170 °C and a treatment time of 20 min.
  • the YR after aging treatment and the fracture stress ratio after aging treatment are determined from the TS, yield stress (YS), and fracture stress after aging treatment measured by a tensile test in accordance with JIS Z 2241:2022, determined using the following expressions.
  • [YR after aging treatment] [YS after aging treatment] / [TS after aging treatment]
  • [Fracture stress ratio after aging treatment] [fracture stress after aging treatment] / [TS after aging treatment]
  • a steel sheet is obtainable that has a TS of 1180 MPa or more, high EL, and also excellent toughness and crash properties after paint baking.
  • the steel sheet of the present disclosure as a material for automotive parts, for example, it is possible to improve fuel efficiency due to an automotive body weight decrease, which can greatly contribute to a decrease in CO 2 emissions. Therefore, the industrial utility value is extremely high.
  • FIG. 1 is a schematic diagram for explaining definitions of entry side intermesh pressing amount and delivery intermesh pressing amount.
  • C is an important basic component of steel.
  • C is an important element that affects the area fraction of tempered martensite and the crash properties after paint baking.
  • C content is less than 0.030 %, the area fraction of tempered martensite decreases, and achieving a TS of 1180 MPa or more becomes difficult. Further, achieving excellent crash properties after paint baking also becomes difficult.
  • the C content exceeds 0.500 %, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, making it difficult to achieve a high EL.
  • the C content is therefore 0.030 % or more and 0.500 % or less.
  • the C content is preferably 0.050 % or more.
  • the C content is more preferably 0.100 % or more.
  • the C content is preferably 0.400 % or less.
  • the C content is more preferably 0.350 % or less.
  • Si is an important basic component of steel.
  • Si suppresses carbide formation during annealing and promotes formation of retained austenite. That is, Si is an important element that affects the area fraction of retained austenite.
  • Si content is less than 0.010 %, achieving a TS of 1180 MPa or more becomes difficult.
  • the Si content exceeds 2.500 %, retained austenite increases excessively, and achieving excellent toughness after paint baking becomes difficult.
  • the Si content is therefore 0.010 % or more and 2.500 % or less.
  • the Si content is preferably 0.050 % or more.
  • the Si content is more preferably 0.100 % or more.
  • the Si content is preferably 2.000 % or less.
  • the Si content is more preferably 1.200 % or less.
  • Mn is an important basic component of steel.
  • Mn is an important element that affects the area fraction of tempered martensite and toughness after paint baking.
  • Mn content is less than 0.10 %, the area fraction of tempered martensite decreases, and achieving a TS of 1180 MPa or more becomes difficult.
  • the Mn content exceeds 5.00 %, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, making it difficult to achieve a high EL.
  • the Mn content is therefore 0.10 % or more and 5.00 % or less.
  • the Mn content is preferably 0.50 % or more.
  • the Mn content is more preferably 0.80 % or more.
  • the Mn content is preferably 4.50 % or less.
  • the Mn content is more preferably 4.00 % or less.
  • P segregates at prior austenite grain boundaries, embrittling the grain boundaries and decreasing steel sheet ultimate deformability. Therefore, when P content becomes excessive, achieving excellent toughness after paint baking becomes difficult.
  • the P content is therefore 0.100 % or less.
  • the P content is preferably 0.070 % or less.
  • a lower limit of the P content is not particularly specified.
  • P is a solid-solution-strengthening element and can increase steel sheet strength. The P content is therefore preferably 0.001 % or more.
  • S exists as a sulfide and decreases steel sheet ultimate deformability. Therefore, when S content becomes excessive, achieving excellent toughness after paint baking becomes difficult.
  • the S content is therefore 0.0200 % or less.
  • the S content is preferably 0.0050 % or less.
  • a lower limit of the S content is not particularly specified. However, in view of production technology constraints, the S content is preferably 0.0001 % or more.
  • N exists as a nitride and decreases steel sheet ultimate deformability. Therefore, when N content becomes excessive, achieving excellent toughness after paint baking becomes difficult.
  • the N content is therefore 0.0100 % or less.
  • the N content is preferably 0.0050 % or less.
  • a lower limit of the N content is not particularly specified. However, in view of production technology constraints, the N content is preferably 0.0001 % or more.
  • O exists as an oxide and decreases steel sheet ultimate deformability. Therefore, when O content becomes excessive, achieving excellent toughness after paint baking becomes difficult.
  • the O content is therefore 0.0100 % or less.
  • the O content is preferably 0.0050 % or less.
  • a lower limit of the O content is not particularly specified. However, in view of production technology constraints, the O content is preferably 0.0001 % or more.
  • Al exists as an oxide and decreases steel sheet ultimate deformability. Therefore, when Al content becomes excessive, achieving excellent toughness after paint baking becomes difficult.
  • the Al content is therefore 1.000 % or less.
  • the Al content is preferably 0.500 % or less.
  • a lower limit of the Al content is not particularly specified. However, in view of production technology constraints, the Al content is preferably 0.001 % or more.
  • the steel sheet according to an embodiment of the present disclosure has a chemical composition including the basic composition above, with the balance being Fe (iron) and inevitable impurity.
  • the steel sheet according to an embodiment of the present disclosure preferably has a chemical composition consisting of the basic composition above, with the balance being Fe and inevitable impurity.
  • the steel sheet according to an embodiment of the present disclosure may contain one or more elements selected from the following as optional additive elements, either alone or in combination.
  • each of Ti, Nb, and V are 0.200 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Ti, Nb, and V are included, the content of each is preferably 0.200 % or less.
  • the content of each of Ti, Nb, and V is respectively more preferably 0.100 % or less.
  • a lower limit of the content of each of Ti, Nb, and V is not particularly specified.
  • Ti, Nb, and V increase the strength of steel sheets by forming fine carbides, nitrides, or carbonitrides during hot rolling or annealing. Therefore, the content of each of Ti, Nb, and V is respectively preferably 0.001 % or more.
  • each of Ta and W are 0.10 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Ta and W are included, the content of each is preferably 0.10 % or less.
  • the content of each of Ta and W is respectively more preferably 0.08 % or less.
  • a lower limit of the content of each of Ta and W is not particularly specified.
  • Ta and W increase the strength of steel sheets by forming fine carbides, nitrides or carbonitrides during hot rolling or annealing. Therefore, the content of each of Ta and W is respectively preferably 0.01 % or more.
  • the B content is preferably 0.0100 % or less.
  • the B content is more preferably 0.0080 % or less.
  • a lower limit of the B content is not particularly specified.
  • B is an element that segregates at an austenite grain boundary during annealing and improves hardenability.
  • the B content is therefore preferably 0.0003 % or more.
  • each of Cr, Mo, and Ni are 1.00 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Cr, Mo, and Ni are included, the content of each is preferably 1.00 % or less. The content of each of Cr, Mo, and Ni is respectively more preferably 0.80 % or less. A lower limit of the content of each of Cr, Mo, and Ni is not particularly specified. However, Cr, Mo, and Ni are elements that improve hardenability. Therefore, the content of each of Cr, Mo, and Ni is respectively preferably 0.01 % or more.
  • the Co content is preferably 0.010 % or less.
  • the Co content is more preferably 0.008 % or less.
  • a lower limit of the Co content is not particularly specified.
  • Co is an element that improves hardenability. The Co content is therefore preferably 0.001 % or more.
  • the Cu content is preferably 1.00 % or less.
  • the Cu content is more preferably 0.80 % or less.
  • a lower limit of the Cu content is not particularly specified.
  • Cu is an element that improves hardenability.
  • the Cu content is therefore preferably 0.01 % or more.
  • the Sn content is preferably 0.200 % or less.
  • the Sn content is more preferably 0.100 % or less.
  • a lower limit of the Sn content is not particularly specified.
  • Sn is an element that improves hardenability and is generally also an element that improves corrosion resistance. The Sn content is therefore preferably 0.001 % or more.
  • the Sb content is preferably 0.200 % or less.
  • the Sb content is more preferably 0.100 % or less.
  • a lower limit of the Sb content is not particularly specified.
  • Sb is an element that controls surface layer softening thickness and allows strength adjustment. The Sb content is therefore preferably 0.001 % or more.
  • each of Ca, Mg, and REM are 0.0100 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Ca, Mg, and REM are included, the content of each is preferably 0.0100 % or less.
  • the content of each of Ca, Mg, and REM is respectively more preferably 0.0050 % or less.
  • a lower limit of the content of each of Ca, Mg, and REM is not particularly specified.
  • Ca, Mg, and REM are elements that spheroidize the shape of nitrides and sulfides and improve steel sheet ultimate deformability. Therefore, the content of each of Ca, Mg, and REM is respectively preferably 0.0005 % or more.
  • each of Zr and Te are 0.100 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Zr and Te are included, the content of each is preferably 0.100 % or less.
  • the content of each of Zr and Te is respectively more preferably 0.080 % or less.
  • a lower limit of the content of each of Zr and Te is not particularly specified.
  • Zr and Te are elements that spheroidize the shape of nitrides and sulfides and improve steel sheet ultimate deformability. Therefore, the content of each of Zr and Te is respectively preferably 0.001 % or more.
  • the Hf content is preferably 0.10 % or less.
  • the Hf content is more preferably 0.08 % or less.
  • a lower limit of the Hf content is not particularly specified.
  • Hf is an element that spheroidizes the shape of nitrides and sulfides and improves steel sheet ultimate deformability. The Hf content is therefore preferably 0.01 % or more.
  • the Bi content is preferably 0.200 % or less.
  • the Bi content is more preferably 0.100 % or less.
  • a lower limit of the Bi content is not particularly specified.
  • Bi is an element that reduces segregation. The Bi content is therefore preferably 0.001 % or more.
  • Fe and inevitable impurity examples include Zn, Pb, As, Ge, Sr, and Cs. Such inevitable impurity is allowed to be included as long as a total amount is 0.100 % or less.
  • the area fraction of each phase is the area ratio occupied by each phase relative to the entire microstructure.
  • the area fraction of tempered martensite is 83 % or more. That is, by making tempered martensite the main phase, in particular by making the area fraction 83 % or more, a TS of 1180 MPa or more is possible to achieve.
  • the area fraction of tempered martensite is therefore 83 % or more.
  • the area fraction of tempered martensite is preferably 85 % or more.
  • the area fraction of tempered martensite is more preferably 87 % or more.
  • An upper limit of the area fraction of tempered martensite is not specifically defined.
  • the area fraction of tempered martensite is, for example, preferably less than 95 %.
  • the area fraction of tempered martensite is more preferably 94 % or less.
  • the area fraction of tempered martensite is even more preferably 93 % or less.
  • the area fraction of retained austenite is less than 3 %. That is, when the area fraction of retained austenite is 3 % or more, achieving excellent toughness after paint baking becomes difficult.
  • One of the causes of decreased toughness after paint baking is that retained austenite transforms into deformation-induced martensite during processing, resulting in high-hardness martensite, which becomes an initiation point of a fracture.
  • the area fraction of retained austenite is therefore less than 3 %.
  • the area fraction of retained austenite is preferably 1 % or less. A lower limit of the area fraction of retained austenite is not specifically defined.
  • the area fraction of retained austenite may be 0 %.
  • Total area fraction of ferrite and bainitic ferrite 5 % or more and less than 15 %
  • the total area fraction of ferrite and bainitic ferrite is more than 5 % and less than 15 %. That is, when the total area fraction of ferrite and bainitic ferrite is 15 % or more, achieving a TS of 1180 MPa or more becomes difficult. On the other hand, when the total area fraction of ferrite and bainitic ferrite is less than 5 %, it becomes difficult to achieve a high EL. Therefore, the total area fraction of ferrite and bainitic ferrite is 5 % or more and less than 15 %.
  • the total area fraction of ferrite and bainitic ferrite is preferably 6 % or more.
  • the total area fraction of ferrite and bainitic ferrite is more preferably 7 % or more.
  • the total area fraction of ferrite and bainitic ferrite is preferably 14 % or less.
  • the total area fraction of ferrite and bainitic ferrite is more preferably 13 % or less.
  • Ferrite and bainitic ferrite may be included individually, or both may be included.
  • the area fraction of residual microstructure other than described above is preferably 5 % or less.
  • Examples of residual microstructure include pearlite, fresh martensite, and acicular ferrite. These residual microstructures may be included as long as the content is 5 % or less, as they do not affect the properties.
  • the area fraction of the residual microstructure may be 0 %.
  • the area fraction of tempered martensite, as well as the total area fraction of ferrite and bainitic ferrite, is measured, for example, as follows.
  • a sample is cut from the steel sheet such that a thickness cross-section parallel to the rolling direction of the steel sheet (L-section) becomes an observation plane.
  • the observation plane of the sample is then polished.
  • the observation plane of the sample is then corroded with 3 vol% nital to reveal the microstructure.
  • a 1/4 sheet thickness position of the steel sheet (a position corresponding to 1/4 of the sheet thickness in the depth direction from a steel sheet surface) is observed at 2000 ⁇ magnification by SEM for ten fields of view.
  • tempered martensite has fine irregularities in the microstructure and contains carbides in the microstructure.
  • ferrite and bainitic ferrite have a flat microstructure in recessed portions and do not contain carbides.
  • the areas occupied by tempered martensite, as well as ferrite and bainitic ferrite are determined.
  • the area occupied by tempered martensite, and the area occupied by ferrite and bainitic ferrite are each divided by the total area of the observed field of view and multiplied by 100. Then, the average values of these are taken as the area fraction of tempered martensite and the total area fraction of ferrite and bainitic ferrite, respectively.
  • the microstructure of steel sheets is normally approximately vertically symmetrical in the thickness direction. Therefore, any one surface of the steel sheet (front or back) can be set as an initiation point of a thickness position (sheet thickness 0 position), such as the 1/4 sheet thickness position or a depth of 100 ⁇ m from the steel sheet surface.
  • the area fraction of retained austenite is measured as follows.
  • the steel sheet is mechanically ground to a depth of 1/4 - 0.1 mm so that the 1/4 sheet thickness position of the steel sheet becomes the observation position, and then further polished by 0.1 mm by chemical polishing.
  • an integrated intensity of the diffraction peaks of bcc iron ⁇ 200 ⁇ , ⁇ 211 ⁇ , and ⁇ 220 ⁇ is compared to that of fcc iron (austenite) ⁇ 200 ⁇ , ⁇ 220 ⁇ , and ⁇ 311 ⁇ using Co K ⁇ radiation with an X-ray diffractometer.
  • a volume fraction of retained austenite is then calculated from the ratio of the integrated intensity of each plane. Then, assuming that the retained austenite is uniform in three dimensions, the volume fraction of the retained austenite is taken as the area fraction of retained austenite.
  • the area fraction of the residual microstructure is determined by subtracting the area fraction of tempered martensite, the total area fraction of ferrite and bainitic ferrite, and the area fraction of retained austenite from 100 %.
  • Area fraction of residual microstructure (%)] 100 - [area fraction of tempered martensite (%)] - [total area fraction of ferrite and bainitic ferrite (%)] - [area fraction of retained austenite (%)]
  • the 20° or greater grain boundary density of tempered martensite is 1.0 ⁇ m/ ⁇ m 2 or more.
  • Large-angle grain boundaries in tempered martensite, particularly 20° or greater grain boundaries in tempered martensite become sites of carbon segregation during paint baking, helping prevent steel sheet fracture. As a result, fracture stress during tensile deformation decreases. Therefore, when 20° or greater grain boundary density in tempered martensite (hereinafter also referred to as large-angle grain boundary density of tempered martensite) is less than 1.0 ⁇ m/ ⁇ m 2 , achieving excellent crash properties after paint baking becomes difficult.
  • the large-angle grain boundary density of tempered martensite is 1.0 ⁇ m/ ⁇ m 2 or more.
  • the large-angle grain boundary density of tempered martensite is preferably 1.2 ⁇ m/ ⁇ m 2 or more.
  • the large-angle grain boundary density of tempered martensite is more preferably 1.3 ⁇ m/ ⁇ m 2 or more.
  • An upper limit of the large-angle grain boundary of tempered martensite is not specifically defined.
  • the large-angle grain boundary density of tempered martensite is preferably 3.0 ⁇ m/ ⁇ m 2 or less.
  • the large-angle grain boundary density of tempered martensite is determined, for example, as follows.
  • a test piece for microstructure observation is collected from the steel sheet.
  • the collected test piece is then polished by colloidal silica vibrational polishing so that the cross-section in the rolling direction (L-section) becomes the observation plane.
  • the observation plane is mirror-finished.
  • EBSD electron backscatter diffraction
  • the step size is set to 0.10 ⁇ m, and the measurement area is 50 ⁇ m square (50 ⁇ m ⁇ 50 ⁇ m). Then, using the analysis software OIM Analysis 7, the obtained local crystal orientation data is analyzed.
  • the analysis of the local crystal orientation data is executed for each of 10 fields of view at the 1/4 sheet thickness position of the steel sheet, and an average value is used. Further, prior to the analysis of the local crystal orientation data, a cleanup process is executed once using a grain dilatation function of the analysis software (grain tolerance angle: 5, minimum grain size: 2, single iteration: ON). Next, the 20° or greater grain boundaries in tempered martensite are displayed, and a total length of the 20° or greater grain boundaries in tempered martensite is determined. Then, by dividing the total length of the 20° or greater grain boundaries in tempered martensite by the area of the measurement region, the large-angle grain boundary density of tempered martensite is determined.
  • KAM(S)/KAM(C) exceeds 1.00.
  • KAM(S) is the KAM value at a depth of 100 ⁇ m from the steel sheet surface
  • KAM(C) is the KAM value at the mid-thickness position of the steel sheet.
  • KAM(S)/KAM(C) is therefore more than 1.00.
  • KAM(S)/KAM(C) is preferably 1.03 or more.
  • An upper limit of KAM(S)/KAM(C) is not particularly defined.
  • KAM(S)/KAM(C) is preferably 1.110 or less.
  • KAM(S) and KAM(C) can be determined, for example, as follows.
  • EBSD measurement is carried out, and the obtained local crystal orientation data is analyzed.
  • the analysis of the local crystal orientation data is executed for 10 fields of view at a depth of 100 ⁇ m from the steel sheet surface and at the mid-thickness position of the steel sheet, and average values are used.
  • a chart of the KAM values of the bcc phase for each position is created, and average values are used as KAM(S) and KAM(C), respectively.
  • the steel sheet according to an embodiment of the present disclosure may include a coated or plated layer on a surface.
  • the coated or plated layer may be on only one surface of the steel sheet or may be on both surfaces.
  • the coated or plated layer is not particularly limited.
  • a galvanized layer with Zn as the main component Zn content of 50.0 mass% or more
  • examples of galvanized layers include hot-dip galvanized layers, galvannealed layers, and electrogalvanized layers.
  • a steel sheet that has a galvanized layer may also be referred to as a galvanized steel sheet.
  • a steel sheet that has a hot-dip galvanized layer, a galvannealed layer, or an electrogalvanized layer may also be referred to as a hot-dip galvanized steel sheet (GI), a galvannealed steel sheet (GA), or an electrogalvanized steel sheet (EG), respectively.
  • GI hot-dip galvanized steel sheet
  • GA galvannealed steel sheet
  • EG electrogalvanized steel sheet
  • Coated or plated layers other than galvanized layers may include aluminum coated or plated layers and alloy coated or plated layers.
  • alloy coated or plated layers examples include hot-dip zinc-aluminum-magnesium alloy coated layers and Zn-Ni electroplated alloy layers.
  • coating weight per side of the coated or plated layer is not particularly limited.
  • the coating weight per side of the coated or plated layer is preferably 20 g/m 2 or more.
  • the coating weight per side is preferably 80 g/m 2 or less.
  • the thickness of the steel sheet according to an embodiment of the present disclosure is not particularly limited.
  • the thickness of the steel sheet is preferably 0.50 mm or more.
  • the thickness of the steel sheet is preferably 2.50 mm or less.
  • the member according to an embodiment of the present disclosure is a member formed using the steel sheet described above as a material.
  • the material, the steel sheet is subjected to at least one of a forming process or a joining process to make the member.
  • the steel sheet described above has a TS of 1180 MPa or more, high EL, and also excellent toughness and crash properties after paint baking. Therefore, the member according to an embodiment of the present disclosure is particularly suitable for application as a material for automotive parts. This allows for improved fuel efficiency due to an automotive body weight decrease, which can greatly contribute to a decrease in CO 2 emissions.
  • the following describes a method of producing a steel sheet according to an embodiment of the present disclosure.
  • each of the temperatures above refers to a surface temperature of the steel sheet. Further, the average heating rate and the average cooling rate are based on the surface temperature of the steel sheet, unless otherwise specified.
  • a blank sheet having the chemical composition described above is prepared.
  • a blank sheet can be prepared by hot rolling a steel slab into a hot-rolled steel sheet, then subjecting the hot-rolled steel sheet to optional pickling and heat treatment, and then cold rolling to obtain a cold-rolled steel sheet.
  • the conditions of these processes are not particularly limited and may follow a conventional method.
  • a method of smelting the steel slab may be any known method, such as by use of a converter, an electric furnace, or the like.
  • the steel slab is preferably smelted by continuous casting to help prevent macro-segregation.
  • hot rolling examples include methods such as rolling the steel slab after heating, direct rolling the steel slab after continuous casting without heating, and rolling the steel slab after applying a short heating treatment following continuous casting.
  • slab heating temperature, slab soaking duration, and coiling temperature in hot rolling are not particularly limited.
  • the slab heating temperature is preferably 1100 °C or more.
  • the slab heating temperature is preferably 1300 °C or less.
  • the slab soaking duration is preferably 30 min or more.
  • the slab soaking duration is preferably 250 min or less.
  • the rolling finish temperature is preferably the Ar 3 transformation temperature or more.
  • the coiling temperature is preferably 350 °C or more.
  • the coiling temperature is preferably 650 °C or less.
  • the Ar 3 transformation temperature is determined by the following expression.
  • Ar 3 transformation temperature (°C) 868 - 396 ⁇ [%C] + 24.6 ⁇ [%Si] - 68.1 ⁇ [%Mn] - 36.1 ⁇ [%Ni] - 20.7 ⁇ [%Cu] - 24.8 ⁇ [%Cr]
  • [%element symbol] in the above expression represents the content in mass% of the element in the chemical composition described above.
  • Pickling is capable of removing oxides from the surface of the hot-rolled steel sheet, and is preferably carried out to secure good chemical convertibility and coating quality in the final steel sheet product. Pickling may be carried out in one or more batches. Further, the hot-rolled steel sheet after pickling may be subjected to heat treatment.
  • the total rolling reduction in the cold rolling is preferably 30 % or more.
  • the total rolling reduction in the cold rolling is preferably 80 % or less. The defined effect can be obtained without limiting the number of rolling passes or the rolling reduction for each pass.
  • the blank sheet prepared in the preparation process is heated to the annealing temperature T1 under a set of conditions including an average heating rate of 5.0 °C/s or less in the temperature range of 700 °C to 750 °C.
  • the annealing temperature T1 is explained in the annealing process described later.
  • the average heating rate in the temperature range of 700 °C to 750 °C affects the density of large-angle grain boundaries of tempered martensite. That is, by setting the average heating rate to 5.0 °C/s or less, the dissolution of carbides is promoted. As a result, prior austenite grain boundaries are refined, and the number of 20° or greater grain boundaries after martensitic transformation increases. Therefore, the density of large-angle grain boundaries of tempered martensite in the final steel sheet product also increases, improving crash properties after paint baking. Accordingly, the average heating rate is 5.0 °C/s or less.
  • the average heating rate is preferably 3.0 °C/s or less.
  • a lower limit of the average heating rate is not specifically defined.
  • the average heating rate is preferably 0.1 °C/s or more.
  • the blank sheet is annealed under a set of conditions including the annealing temperature T1 being 750 °C or more and 850 °C or less, and annealing time t1 being 10 s or longer and 1000 s or shorter.
  • the annealing temperature T1 When the annealing temperature T1 is less than 750 °C, the total area fraction of ferrite and bainitic ferrite becomes 15 % or more, and achieving a TS of 1180 MPa or more becomes difficult. On the other hand, when the annealing temperature T1 exceeds 850 °C, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, making it difficult to achieve a high EL.
  • the annealing temperature T1 is therefore 750 °C or more and 850 °C or less.
  • the annealing temperature T1 is preferably 760 °C or more.
  • the annealing temperature T1 is more preferably 770 °C or more.
  • the annealing temperature T1 is preferably 840 °C or less.
  • the annealing temperature T1 is more preferably 830 °C or less.
  • the annealing temperature referred to here is the holding temperature during the annealing process. Further, the annealing temperature may remain constant during holding. Further, the annealing temperature is the temperature range of 750 °C or more and 850 °C or less, and when temperature fluctuation is within ⁇ 10 °C of the set temperature, the annealing temperature does not have to be constant during holding.
  • the annealing time t1 When the annealing time t1 is less than 10 s, the total area fraction of ferrite and bainitic ferrite becomes 15 % or more, and achieving a TS of 1180 MPa or more becomes difficult. On the other hand, when the annealing time t1 exceeds 1000 s, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, making it difficult to achieve a high EL.
  • the annealing time t1 is therefore 10 s or longer and 1000 s or shorter.
  • the annealing time t1 is preferably 30 s or longer.
  • the annealing time t1 is preferably 800 s or shorter.
  • the annealing time t1 referred to here is the holding time at the annealing temperature T1.
  • the blank sheet is subjected to bending once or more using a roller that has a radius of 800 mm or less in the temperature range from the annealing temperature T1 to 700 °C.
  • the inventors found that carrying out bending in the temperature range from the annealing temperature T1 to 700 °C affects the large-angle grain boundary density of tempered martensite.
  • carrying out bending using a roller that has a radius of 800 mm or less in the bending temperature range promotes martensitic transformation nucleation.
  • martensite is refined, and 20° or greater grain boundaries after martensitic transformation increase. Therefore, the density of large-angle grain boundaries of tempered martensite in the final steel sheet product also increases, improving crash properties after paint baking.
  • the number of times bending using a roller that has a radius of 800 mm or less in the bending temperature range (hereinafter also referred to as bending count) is set to be once or more.
  • the radius of the roller used for bending is preferably 600 mm or less.
  • a lower limit of the radius of the roller used for bending is not particularly restricted.
  • the radius of the roller used for bending is preferably 100 mm or more.
  • the number of bends may be one or more.
  • the number of bends is preferably two or more.
  • An upper limit of the number of bends is not specifically defined.
  • the number of bends is preferably 15 or fewer.
  • the bending may be carried out by bending in one direction with a roller and then bending back the same amount in the opposite direction. In such a case, the number of bends is counted as two (one for bending and one for bending back).
  • the bending angle is preferably 80° or more.
  • the bending angle is preferably 110° or less. This results in a greater effect of promoting martensitic transformation nucleation.
  • the bending angle is the angle (acute angle) formed between the sheet passing direction of the steel sheet on the roller entry side and the sheet passing direction of the steel sheet on the roller delivery side.
  • the blank sheet is cooled to a first cooling end temperature under a set of conditions including an average cooling rate of 0.5 °C/s or more and less than 10.0 °C/s in a temperature range from 700 °C to 550 °C.
  • Average cooling rate in temperature range from 700 °C to 550 °C: 0.5 °C/s or more and less than 10.0 °C/s]
  • first average cooling rate When the average cooling rate in the temperature range from 700 °C to 550 °C (hereinafter also referred to as first average cooling rate) is 10.0 °C/s or more, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, and achieving a high EL becomes difficult. On the other hand, when the first average cooling rate is less than 0.5 °C/s, the total area fraction of ferrite and bainitic ferrite becomes 15 % or more, and achieving a TS of 1180 MPa or more becomes difficult.
  • the first average cooling rate is therefore 0.5 °C/s or more and less than 10.0 °C/s.
  • the first average cooling rate is preferably 1.0 °C/s or more.
  • the first average cooling rate is preferably 8.0 °C/s or less.
  • the first cooling end temperature may be, for example, from 550 °C to 300 °C.
  • a coating or plating treatment may be applied to the blank sheet between the first cooling process and the second cooling process described later. Details about the coating or plating treatment are described later.
  • the blank sheet is cooled to the second cooling end temperature under a set of conditions including an average cooling rate of 300 °C/s or more in a temperature range from 300 °C to 100 °C, and a tension of 5 MPa or more applied to the blank sheet in the temperature range from 300 °C to 100 °C.
  • the average cooling rate in the temperature range from 300 °C to 100 °C (hereinafter also referred to as second average cooling rate) is less than 300 °C/s, the area fraction of retained austenite becomes 3 % or more, and achieving excellent toughness after paint baking becomes difficult.
  • the second average cooling rate is therefore 300 °C/s or more.
  • the second average cooling rate is preferably 800 °C/s or more.
  • An upper limit of the second average cooling rate is not specifically defined.
  • the second average cooling rate is preferably 2000 °C/s or less.
  • applied tension to the blank sheet during cooling in the temperature range from 300 °C to 100 °C affects the large-angle grain boundary density of tempered martensite.
  • the tension applied to the blank sheet in the temperature range from 300 °C to 100 °C (hereinafter also referred to simply as applied tension) is 5 MPa or more, martensitic transformation is promoted.
  • martensite is refined, and 20° or greater grain boundaries after martensitic transformation increase. Therefore, the density of large-angle grain boundaries of tempered martensite in the final steel sheet product also increases, improving crash properties after paint baking.
  • the applied tension is 5 MPa or more.
  • the applied tension is preferably 10 MPa or more.
  • An upper limit of the applied tension is not specifically defined.
  • the applied tension is preferably 100 MPa or less.
  • the second cooling end temperature may be, for example, less than 100 °C.
  • the second cooling end temperature may be, for example, around room temperature.
  • the bending in the bending process described above increases the number of nucleation sites, which are initiation points of martensitic transformation.
  • the application of tension in the second cooling process promotes the martensitic transformation itself. That is, the effects obtained from both are different.
  • the blank sheet is tempered under a set of conditions including the tempering temperature T2 being 100 °C or more and 400 °C or less, and tempering time t2 being 10 s or longer and 10,000 s or shorter.
  • Tempered martensite is formed by tempering treatment, where martensite is tempered.
  • the tempering temperature T2 is less than 100 °C, martensite is not sufficiently tempered, resulting in a microstructure mainly composed of quenched martensite. In such a microstructure mainly composed of quenched martensite, excellent toughness after paint baking cannot be obtained.
  • the tempering temperature T2 exceeds 400 °C, tempering of martensite progresses excessively, and achieving a TS of 1180 MPa or more becomes difficult.
  • the tempering temperature T2 is therefore 100 °C or more and 400 °C or less.
  • the tempering temperature T2 is preferably 150 °C or more.
  • the tempering temperature T2 is preferably 350 °C or less.
  • the tempering temperature referred to here is the holding temperature during the tempering process.
  • the tempering temperature may be constant during holding. Further, the tempering temperature is in the range from 100 °C or more to 400 °C or less, and when temperature fluctuation is within ⁇ 10 °C of the set temperature, the tempering temperature does not have to be constant during holding.
  • tempered martensite is formed by tempering treatment, where martensite is tempered.
  • the tempering time t2 is shorter than 10 s, martensite is not sufficiently tempered, resulting in a microstructure mainly composed of quenched martensite. In such a microstructure mainly composed of quenched martensite, excellent toughness after paint baking cannot be obtained.
  • the tempering time t2 exceeds 10,000 s, tempering of martensite progresses excessively, and achieving a TS of 1180 MPa or more becomes difficult.
  • the tempering time t2 is 10 s or longer and 10,000 s or shorter.
  • the tempering time t2 is preferably 50 s or longer.
  • the tempering time t2 is preferably 5000 s or shorter.
  • the tempering time t2 refers to the holding time at the tempering temperature T2.
  • the cooling after tempering is not specifically defined. For example, it is sufficient to cool by any method according to a conventional method.
  • the cooling end temperature after tempering may be, for example, around room temperature.
  • a coating or plating treatment may be applied to the blank sheet between the tempering process and the straightening process described below. Details about the coating or plating treatment are described later.
  • the blank sheet is subjected to straightening by leveling (using a leveler). At this time, satisfying the following conditions is extremely important in the method of producing the steel sheet according to an embodiment of the present disclosure.
  • the straightening start temperature is therefore 100 °C or less.
  • the straightening start temperature is preferably 80 °C or less.
  • a lower limit of the straightening start temperature is not specifically defined.
  • the straightening start temperature is preferably -10 °C or more.
  • the entry side intermesh pressing amount When the entry side intermesh pressing amount is less than 4.0 mm, the amount of processing is insufficient. As a result, KAM(S)/KAM(C) becomes 1.00 or less, and the crash properties after paint baking decrease.
  • An upper limit of the entry side intermesh pressing amount is 10.0 mm or less in view of production technology constraints.
  • the entry side intermesh pressing amount is therefore 4.0 mm or more and 10.0 mm or less.
  • the entry side intermesh pressing amount is preferably 5.0 mm or more.
  • the delivery intermesh pressing amount is less than 1.0 mm, the amount of processing is insufficient. As a result, KAM(S)/KAM(C) becomes 1.00 or less, and the crash properties after paint baking decrease.
  • An upper limit of the delivery intermesh pressing amount is 10.0 mm or less in view of production technology constraints. The delivery intermesh pressing amount is therefore 1.0 mm or more and 10.0 mm or less.
  • the entry side intermesh pressing amount refers to the pressing amount of the second roller from the entry side (roller 2 in FIG. 1 ) against the steel sheet plane (the surface of the steel sheet where roller 2 is disposed) in leveling.
  • the delivery intermesh pressing amount refers to the pressing amount of the second roller from the delivery side (roller 8 in FIG. 1 ) against the steel sheet plane (the surface of the steel sheet where roller 8 is disposed) in leveling.
  • the number of rollers in the leveling (leveler) is not particularly limited. For example, five or more rollers is preferred.
  • the entry side tension When the entry side tension is less than 20 MPa, the amount of processing is insufficient. Therefore, KAM(S)/KAM(C) becomes 1.00 or less, and the crash properties after paint baking decrease.
  • the upper limit of the entry side tension is 500 MPa in view of production technology constraints. Accordingly, the entry side tension is 20 MPa or more and 500 MPa or less.
  • the entry side tension is preferably 100 MPa or more.
  • the delivery tension is higher than the entry side tension.
  • the delivery intermesh pressing amount is less than 25 MPa, the amount of processing is insufficient. Therefore, KAM(S)/KAM(C) becomes 1.00 or less, and the crash properties after paint baking decrease.
  • the upper limit of the delivery tension is 550 MPa or less in view of production technology constraints. Accordingly, the delivery tension is 25 MPa or more and 550 MPa or less.
  • the delivery tension is preferably 100 MPa or more.
  • the steel sheet may be subjected to coating or plating treatment.
  • Coating or plating treatment is not particularly limited.
  • coating or plating treatment include galvanizing treatment such as hot-dip galvanizing treatment, galvannealing treatment, and electrogalvanization treatment.
  • examples of coating or plating treatment include aluminum coating or plating treatment and alloy coating or plating treatment.
  • alloy coating or plating treatment include hot-dip zinc-aluminum-magnesium alloy coating treatment and Zn-Ni electro-alloy plating treatment. Treatment conditions may follow conventional methods.
  • the coating or plating treatment is preferably carried out between the first cooling process and the second cooling process, or between the tempering process and the straightening process.
  • hot-dip galvanizing treatment or galvannealing treatment is preferably carried out between the first cooling process and the second cooling process.
  • electrogalvanization treatment or Zn-Ni electro-alloy plating treatment is preferably carried out between the tempering process and the straightening process.
  • the series of treatments including the heating process, the annealing process, and the coating or plating treatment process is preferably carried out on a continuous galvanizing line (CGL).
  • wiping may be carried out for adjusting the coating amount.
  • Conditions other than those described above are not particularly limited, and a conventional method may be used. According to the method of producing the steel sheet according to an embodiment of the present disclosure described above, a steel sheet is obtainable that has a TS of 1180 MPa or more, high EL, and also excellent toughness and crash properties after paint baking. The obtained steel sheet may be suitably used as a material for automotive parts, for example.
  • the method of producing a member according to an embodiment of the present disclosure includes process of at least one of forming or joining the steel sheet described above to make the member.
  • a forming method is not particularly limited, and a typical processing method such as press forming may be used, for example.
  • a joining method is also not particularly limited, and for example, typical welding such as spot welding, laser welding, arc welding, and the like, rivet joining, swaging joining, and the like may be used.
  • Forming and joining conditions are not particularly limited and may follow a conventional method.
  • the first cooling end temperature in each case was set to 550 °C to 300 °C.
  • Both the second cooling end temperature and the cooling end temperature after tempering were set to room temperature.
  • the bending angle in the bending was set to 80° to 110°.
  • some of the steel sheets (those listed as GI, GA, and EG in Table 2) were subjected to coating or plating treatment. Among these, for those listed as GI and GA in Table 2, coating treatment was carried out between the first cooling process and the second cooling process. For those listed as EG in Table 2, plating treatment was carried out between the tempering process and the straightening process. Conditions not specified were followed according to conventional methods.
  • a JIS No. 5 test piece (gauge length: 50 mm, parallel portion width: 25 mm) was taken so that the direction perpendicular to the rolling direction of the steel sheet was the longitudinal direction of the test piece.
  • a tensile test was conducted according to JIS Z 2241:2022 using the test piece, and TS and EL were measured.
  • the crosshead speed was set to 1.67 ⁇ 10 -1 mm/s. Evaluation was based on the following criteria.
  • the EL measured in the above tensile tests was evaluated according to the following criteria.
  • a plurality of sheets were stacked and fastened with bolts.
  • a V-notch having a depth of 2 mm was applied to the stacked steel sheets, and a stacked Charpy test piece (hereinafter also referred to simply as the test piece) was prepared.
  • the number of stacked steel sheets was set to the number that most closely approaches a thickness of 10 mm for the test piece (when there were two numbers that were closest to 10 mm, the smaller number was chosen). For example, when the thickness of the steel sheet was 1.2 mm, eight sheets of the steel sheet were stacked together. That is, the thickness of the test piece was 9.6 mm.
  • test piece was prepared so that the sheet transverse direction of the steel sheet (direction perpendicular to the rolling direction) was the longitudinal direction of the test piece.
  • the prepared test piece was then subjected to aging treatment at a treatment temperature of 170 °C for a treatment time of 20 min.
  • a Charpy impact test was carried out in a test temperature range of -120 °C to +120 °C. From the obtained percent brittle fracture, a transition curve was determined, and the temperature at which the percent brittle fracture reached 50 % was defined as the brittle-ductile transition temperature. Based on the following criteria, the toughness after paint baking was evaluated. Other than the above conditions, JIS Z 2242:2018 was followed.
  • the obtained steel sheets were each subjected to aging treatment at a treatment temperature of 170 °C for a treatment time of 20 min.
  • a JIS No. 5 test piece (gauge length: 50 mm, parallel portion width: 25 mm) was taken so that the direction perpendicular to the rolling direction of the steel sheet was the longitudinal direction of the test piece.
  • a tensile test was carried out according to JIS Z 2241:2022 in the same manner as in the TS evaluation described above, measuring the TS, yield stress (YS), and fracture stress after aging treatment. Based on the following criteria, the crash properties after paint baking were then evaluated.
  • the YR and fracture stress ratio after aging treatment are determined by the following expressions, respectively.
  • [YR after aging treatment] [YS after aging treatment] / [TS after aging treatment]
  • [Fracture stress ratio after aging treatment] [fracture stress after aging treatment] / [TS after aging treatment]
  • the fracture stress is the stress at the fracture point in the tensile test (the stress applied when the test piece fractures).
  • Table 2 No. Steel sample ID Heating process Annealing process Bending process First cooling process Second cooling process Tempering process Straightening process Type* Remarks Average heating rate (°C/S ) Annealing temp. T1 (°C) Annealing time t1 (s) Number of bends (times) First average cooling rate (° C/s) Second average cooling rate (°C/s) Applied tension (MPa) Tempering temp. T2 (°C) Tempering time t2 (s) Straightening start temp.
  • Tempered M tempered martensite, retained ⁇ : retained austenite, F: ferrite, B: bainitic ferrite No. Steel sample ID Microstructure * Evaluation result Remarks Area fraction Large-angle grain boundary density of tempered M ( ⁇ d/ ⁇ m 2 ) KAM(S) /KAM(C) TS EL Toughness after paint baking Crash properties after paint baking Tempered M (%) Retained ⁇ (%) F + B (%) TS (MPa) Evaluation EL (%) Evaluation Brittle-ductile transition temp.
  • Tempered M tempered martensite, retained ⁇ : retained austenite, F: ferrite, B: bainitic ferrite No. Steel sample ID Microstructure* Evaluation result Remarks Area fraction Large-angle grain boundary density of tempered M ( ⁇ m/ ⁇ m 2 ) KAM(S) /KAM(C) TS EL Toughness after paint baking Crash properties after paint baking Tempered M (%) Retained ⁇ (%) F + B (%) TS (MPa) Evaluation EL (%) Evaluation Brittle-ductile transition temp.
  • TS, EL as erll as toughness and crash properties after paint baking, all reached passing criteria.
  • members obtained by forming and members obtained by joining all had a target shape without crack occurrence, and TS, EL, as well as toughness and crash properties after paint baking, all reached passing criteria.

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Abstract

Provided is a steel sheet that has a TS of 1180 MPa or more, high EL, and also excellent toughness and crash properties after paint baking. The steel sheet has a defined chemical composition and a microstructure where an area fraction of tempered martensite is 83 % or more, an area fraction of retained austenite is less than 3 %, a total area fraction of bainitic ferrite and ferrite 5 % or more and less than 15 %, and a 20° or greater grain boundary density in tempered martensite is 1.0 µm/µm2 or more, satisfying the following Expression (1): KAM S / KAM C > 1.00

Description

    TECHNICAL FIELD
  • The present disclosure relates to a steel sheet, a member using the steel sheet as material, and methods of producing same.
  • BACKGROUND
  • Higher strength steel sheets as material for automotive parts are being developed to both decrease CO2 emissions by decreasing automobile body weight and improve crashworthiness. Further, new laws and regulations are being introduced one after another. As a result, in the main structural parts of automobiles, the application of steel sheets that have a tensile strength (hereinafter also referred to as TS) of 1180 MPa or more is increasing.
  • Further, steel sheets used as material for automotive parts, for example, automobile frame parts such as bumpers, are often required, from the viewpoint of press formability, to have high elongation (hereinafter, also referred to as EL).
  • As a steel sheet used as material for an automotive part, for example, Patent Literature (PTL) 1 describes:
    • "a steel sheet comprising: a chemical composition containing, in mass%,
    • C: 0.12 % or more and 0.40 % or less,
    • Si: 0.01 % or more and 1.5 % or less,
    • Mn: more than 1.7 % and 3.5 % or less,
    • P: 0.05 % or less,
    • S: 0.010 % or less,
    • sol.Al: 1.00 % or less,
    • N: 0.010 % or less,
    • B: 0.0002 % or more and 0.0050 % or less, and
    • one or both of Nb and Ti for a total of 0.010 % or more and 0.080 % or less, with the balance being Fe and inevitable impurity; and
    • a steel microstructure that has a martensite area fraction of 70 % or more, a bainite area fraction of 30 % or less, and a total area fraction of ferrite and retained austenite of 10 % or less, wherein
    • a number density of carbides that have a major axis length of 0.5 µm or more at a 1/4 sheet thickness position of the steel sheet is 60,000/mm2 or less,
    • a number density of inclusion particles that have a circle equivalent diameter of 4.0 µm or more in a range from 1/4 to 3/4 sheet thickness of the steel sheet is 10/mm2 or more and 30/mm2 or less,
    • a number density of inclusion particles that have a circle equivalent diameter of 4.0 µm or more in a range from a surface to 1/4 sheet thickness of the steel sheet is 27/mm2 or less, and
    • tensile strength is 1310 MPa or more."
  • PTL 2 describes:
    • "a steel sheet comprising: a chemical composition containing, in mass%,
    • C: 0.05 % to 0.40 %,
    • Si: 0.05 % to 3.0 %,
    • Mn: 1.5 % to 3.5 %,
    • Al: 1.5 % or less,
    • N: 0.010 % or less,
    • P: 0.10 % or less,
    • S: 0.005 % or less,
    • Cr, Cu, Ni, Sn, and Mo: total of 0.0 % to 1.0 %,
    • B: 0.000 % to 0.005 %,
    • Ca: 0.000 % to 0.005 %,
    • Ce: 0.000 % to 0.005 %, and
    • La: 0.000 % to 0.005 %,
    • and further containing one or more selected from the group consisting of
    • Nb: 0.0002 % to 0.04 %,
    • Ti: 0.0002 % to 0.08 %, and
    • V and Ta: a total of 0.01 % to 0.3 %,
    • with the balance being Fe and impurity; and
    • a steel microstructure represented by, in area%,
    • first martensite with two or more iron carbides having a circle equivalent diameter from 2 nm to 500 nm: 20 % to 95 %,
    • ferrite: 15 % or less,
    • retained austenite: 15 % or less, and
    • residual microstructure: bainite or second martensite with less than two iron carbides having a circle equivalent diameter from 2 nm to 500 nm, or both of these, wherein
    • a total area fraction of ND//<111> orientation grains and ND//<100> orientation grains is 40 % or less,
    • an amount of solute C is 0.44 ppm or more,
    • the ND//<111> orientation grains are crystal grains that have a crystal orientation parallel to the normal direction of the sheet surface, with a deviation of 10° or less from the <111> direction, and
    • the ND//<100> orientation grains are crystal grains that have a crystal orientation parallel to the normal direction of the sheet surface, with a deviation of 10° or less from the <100> direction."
  • PTL 3 describes:
    • "a steel sheet comprising: a chemical composition containing, in mass%,
    • C: 0.09 % or more and 0.37 % or less,
    • Si: more than 0.70 % and 2.00 % or less,
    • Mn: 2.60 % or more and 3.60 % or less,
    • P: 0.001 % or more and 0.100 % or less,
    • S: 0.0200 % or less,
    • Al: 0.010 % or more and 1.000 % or less, and
    • N: 0.0100 % or less, with the balance being Fe and inevitable impurity; and
    • a steel microstructure that has an area fraction of martensite with a carbon concentration greater than 0.7 × [%C] and less than 1.5 × [%C] of 55 % or more,
    • an area fraction of tempered martensite with a carbon concentration of 0.7 × [%C] or less of 5 % or more and 40 % or less,
    • a ratio of carbon concentration in retained austenite to a volume fraction of retained austenite of 0.05 or more and 0.40 or less, and
    • an average grain size of the martensite and the tempered martensite of 5.3 µm or less, wherein
    • the steel microstructure further has a surface layer softening thickness of 10 µm or more and 100 µm or less, and
    • tensile strength is 1180 MPa or more,
    • where [%C] represents content in mass% of the component element C in the steel."
    CITATION LIST Patent Literature
    • PTL 1: JP 7001197 B2
    • PTL 2: JP 6497443 B2
    • PTL 3: JP 6747612 B2
    SUMMARY (Technical Problem)
  • Automotive parts often undergo paint baking. Here, toughness and crash properties of a steel sheet may change significantly before and after paint baking. Therefore, in recent years, steel sheets used as material for automotive parts are also required to have excellent toughness and crash properties after paint baking for further improvement of automobile safety.
  • However, none of the steel sheets described in PTL 1 to PTL 3 take into account toughness and crash properties after paint baking. Accordingly, it is currently desirable to develop a steel sheet that has a TS of 1180 MPa or more, high EL, and also excellent toughness and crash properties after paint baking.
  • In view of the above circumstances, it would be helpful to provide a steel sheet that has a TS of 1180 MPa or more, high EL, and also excellent toughness and crash properties after paint baking, along with an advantageous method of producing the steel sheet.
  • Further, it would be helpful to provide a member using the steel sheet as a material and a method of producing the member.
  • Here, TS is measured by a tensile test in accordance with JIS Z 2241:2022.
  • High EL means an EL of 10 % or more. Further, EL is measured by a tensile test in accordance with JIS Z 2241:2022.
  • Excellent toughness after paint baking means that a brittle-ductile transition temperature after aging treatment is -40 °C or lower. Here, the aging treatment conditions are a treatment temperature of 170 °C and a treatment time of 20 min. Further, the brittle-ductile transition temperature is measured by the Charpy impact test in accordance with JIS Z 2242:2018.
  • Excellent crash properties after paint baking means that a YR after aging treatment is 0.85 or more, and a fracture stress ratio after aging treatment is 0.90 or less. Here, the aging treatment conditions are a treatment temperature of 170 °C and a treatment time of 20 min. The YR after aging treatment and the fracture stress ratio after aging treatment are determined from the TS, yield stress (YS), and fracture stress after aging treatment measured by a tensile test in accordance with JIS Z 2241:2022, determined using the following expressions. [YR after aging treatment] = [YS after aging treatment] / [TS after aging treatment] [Fracture stress ratio after aging treatment] = [fracture stress after aging treatment] / [TS after aging treatment]
  • Details of the measurement methods are described in the EXAMPLES section below.
  • (Solution to Problem)
  • The inventors conducted intensive studies to achieve the above, and made the following discoveries:
    1. (A) To obtain a TS of 1180 MPa or more, it is important that the area fraction of tempered martensite is 83 % or more and the total area fraction of ferrite and bainitic ferrite is less than 15 %. This allows for obtaining a TS of 1180 MPa or more while securing defined required properties.
    2. (B) To obtain a high EL, it is important that the total area fraction of ferrite and bainitic ferrite is 5 % or more. This makes it possible to obtain a high EL while securing defined required properties.
    3. (C) To obtain excellent toughness after paint baking, it is important to have an area fraction of retained austenite of less than 3 %, and a 20° or greater grain boundary density in tempered martensite of 1.0 µm/µm2 or more. This allows for obtaining excellent toughness after paint baking while securing the defined required properties.
    4. (D) To obtain excellent crash properties after paint baking, it is important to have a 20° or greater grain boundary density in tempered martensite of 1.0 µm/µm2 and to satisfy the following Expression (1). This allows for obtaining excellent crash properties after paint baking while securing defined required properties. KAM S / KAM C > 1.00
  • Here,
    • KAM(S) is KAM value at a depth of 100 µm from a surface of the steel sheet, and
    • KAM(C) is KAM value at a mid-thickness position of the steel sheet.
  • The present disclosure is based on these discoveries and further studies.
  • Primary features of the present disclosure are as follows.
    1. 1. A steel sheet comprising: a chemical composition containing (consisting of), in mass%,
      • C: 0.030 % or more and 0.500 % or less,
      • Si: 0.010 % or more and 2.500 % or less,
      • Mn: 0.10 % or more and 5.00 % or less,
      • P: 0.100 % or less,
      • S: 0.0200 % or less,
      • N: 0.0100 % or less,
      • O: 0.0100 % or less, and
      • Al: 1.000 % or less,
      • with the balance being Fe and inevitable impurity; and a steel microstructure wherein
      • area fraction of tempered martensite is 83 % or more,
      • area fraction of retained austenite is less than 3 %,
      • total area fraction of ferrite and bainitic ferrite is 5 % or more and less than 15 %,
      • 20° or greater grain boundary density in the tempered martensite is 1.0 µm/µm2 or more, and
      • the following Expression (1) is satisfied, KAM S / KAM C > 1.00 where
        • KAM(S) is an average KAM value at a depth of 100 µm from a surface of the steel sheet, and
        • KAM(C) is an average KAM value at a mid-thickness position of the steel sheet.
    2. 2. The steel sheet according to 1, above, wherein the chemical composition further contains, in mass%, at least one selected from the group consisting of
      • Ti: 0.200 % or less,
      • Nb: 0.200 % or less,
      • V: 0.200 % or less,
      • Ta: 0.10 % or less,
      • W: 0.10 % or less,
      • B: 0.0100 % or less,
      • Cr: 1.00 % or less,
      • Mo: 1.00 % or less,
      • Ni: 1.00 % or less,
      • Co: 0.010 % or less,
      • Cu: 1.00 % or less,
      • Sn: 0.200 % or less,
      • Sb: 0.200 % or less,
      • Ca: 0.0100 % or less,
      • Mg: 0.0100 % or less,
      • REM: 0.0100 % or less,
      • Zr: 0.100 % or less,
      • Te: 0.100 % or less,
      • Hf: 0.10 % or less, and
      • Bi: 0.200 % or less.
    3. 3. The steel sheet according to 1 or 2, above, further comprising a coated or plated layer on a surface.
    4. 4. A member formed using the steel sheet according to any one of 1 to 3, above.
    5. 5. A method of producing the steel sheet according to any one of 1 to 3, above, the method comprising:
      • a preparation process of preparing a blank sheet having the chemical composition according to 1 or 2, above;
      • a heating process of heating the blank sheet under a set of conditions including an average heating rate in a temperature range from 700 °C to 750 °C of 5.0 °C/s or less, and
      • heating to an annealing temperature T1;
      • an annealing process of annealing the blank sheet under a set of conditions including the annealing temperature T1 being 750 °C or more and 850 °C or less, and
      • an annealing time t1 of 10 s or longer and 1000 s or shorter;
      • a bending process of applying bending once or more to the blank sheet using a roller that has a radius of 800 mm or less in a temperature range from the annealing temperature T1 to 700 °C;
      • a first cooling process of cooling the blank sheet under a set of conditions including an average cooling rate in a temperature range from 700 °C to 550 °C of 0.5 °C/s or more and less than 10.0 °C/s,
      • to a first cooling end temperature;
      • a second cooling process of cooling the blank sheet under a set of conditions including an average cooling rate in a temperature range from 300 °C to 100 °C of 300 °C/s or more, and
      • applying tension to the blank sheet in the temperature range from 300 °C to 100 °C of 5 MPa or more,
        to a second cooling end temperature;
      • a tempering process of tempering the blank sheet under a set of conditions including a tempering temperature T2 of 100 °C or more and 400 °C or less, and
      • a tempering time t2 of 10 s or longer and 10,000 s or shorter; and
      • a straightening process of applying straightening to the blank sheet by leveling under a set of conditions including a straightening start temperature of 100 °C or less,
      • an entry side intermesh pressing amount of 4.0 mm or more and 10.0 mm or less,
      • a delivery intermesh pressing amount of 1.0 mm or more and 10.0 mm or less,
      • an entry side tension of 20 MPa or more and 500 MPa or less, and
      • a delivery tension of 25 MPa or more and 550 MPa or less.
    6. 6. The method of producing a steel sheet according to 5, above, further comprising a coating or plating process of applying a coating or plating treatment to the blank sheet between the first cooling process and the second cooling process, or between the tempering process and the straightening process.
    7. 7. A method of producing a member, wherein the steel sheet according to any one of 1 to 3, above, is subjected to at least one of a forming process or a joining process to produce the member.
    (Advantageous Effect)
  • According to the present disclosure, a steel sheet is obtainable that has a TS of 1180 MPa or more, high EL, and also excellent toughness and crash properties after paint baking. By applying the steel sheet of the present disclosure as a material for automotive parts, for example, it is possible to improve fuel efficiency due to an automotive body weight decrease, which can greatly contribute to a decrease in CO2 emissions. Therefore, the industrial utility value is extremely high.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • In the accompanying drawings:
    FIG. 1 is a schematic diagram for explaining definitions of entry side intermesh pressing amount and delivery intermesh pressing amount.
  • DETAILED DESCRIPTION
  • The following describes embodiments of the present disclosure.
  • [1] Steel sheet
  • First, the chemical composition of a steel sheet according to an embodiment of the present disclosure is described. Hereinafter, although the unit in all chemical compositions is "mass%", this may be indicated simply as "%", unless otherwise specified.
  • [C: 0.030 % or more and 0.500 % or less]
  • C is an important basic component of steel. In particular, in the steel sheet according to an embodiment of the present disclosure, C is an important element that affects the area fraction of tempered martensite and the crash properties after paint baking. When C content is less than 0.030 %, the area fraction of tempered martensite decreases, and achieving a TS of 1180 MPa or more becomes difficult. Further, achieving excellent crash properties after paint baking also becomes difficult. On the other hand, when the C content exceeds 0.500 %, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, making it difficult to achieve a high EL. The C content is therefore 0.030 % or more and 0.500 % or less. The C content is preferably 0.050 % or more. The C content is more preferably 0.100 % or more. The C content is preferably 0.400 % or less. The C content is more preferably 0.350 % or less.
  • [Si: 0.010 % or more and 2.500 % or less]
  • Si is an important basic component of steel. In particular, in the steel sheet according to an embodiment of the present disclosure, Si suppresses carbide formation during annealing and promotes formation of retained austenite. That is, Si is an important element that affects the area fraction of retained austenite. When Si content is less than 0.010 %, achieving a TS of 1180 MPa or more becomes difficult. On the other hand, when the Si content exceeds 2.500 %, retained austenite increases excessively, and achieving excellent toughness after paint baking becomes difficult. The Si content is therefore 0.010 % or more and 2.500 % or less. The Si content is preferably 0.050 % or more. The Si content is more preferably 0.100 % or more. The Si content is preferably 2.000 % or less. The Si content is more preferably 1.200 % or less.
  • [Mn: 0.10 % or more and 5.00 % or less]
  • Mn is an important basic component of steel. In particular, in the steel sheet according to an embodiment of the present disclosure, Mn is an important element that affects the area fraction of tempered martensite and toughness after paint baking. When Mn content is less than 0.10 %, the area fraction of tempered martensite decreases, and achieving a TS of 1180 MPa or more becomes difficult. On the other hand, when the Mn content exceeds 5.00 %, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, making it difficult to achieve a high EL. The Mn content is therefore 0.10 % or more and 5.00 % or less. The Mn content is preferably 0.50 % or more. The Mn content is more preferably 0.80 % or more. The Mn content is preferably 4.50 % or less. The Mn content is more preferably 4.00 % or less.
  • [P: 0.100 % or less]
  • P segregates at prior austenite grain boundaries, embrittling the grain boundaries and decreasing steel sheet ultimate deformability. Therefore, when P content becomes excessive, achieving excellent toughness after paint baking becomes difficult. The P content is therefore 0.100 % or less. The P content is preferably 0.070 % or less. A lower limit of the P content is not particularly specified. However, P is a solid-solution-strengthening element and can increase steel sheet strength. The P content is therefore preferably 0.001 % or more.
  • [S: 0.0200 % or less]
  • S exists as a sulfide and decreases steel sheet ultimate deformability. Therefore, when S content becomes excessive, achieving excellent toughness after paint baking becomes difficult. The S content is therefore 0.0200 % or less. The S content is preferably 0.0050 % or less. A lower limit of the S content is not particularly specified. However, in view of production technology constraints, the S content is preferably 0.0001 % or more.
  • [N: 0.0100 % or less]
  • N exists as a nitride and decreases steel sheet ultimate deformability. Therefore, when N content becomes excessive, achieving excellent toughness after paint baking becomes difficult. The N content is therefore 0.0100 % or less. The N content is preferably 0.0050 % or less. A lower limit of the N content is not particularly specified. However, in view of production technology constraints, the N content is preferably 0.0001 % or more.
  • [O: 0.0100 % or less]
  • O exists as an oxide and decreases steel sheet ultimate deformability. Therefore, when O content becomes excessive, achieving excellent toughness after paint baking becomes difficult. The O content is therefore 0.0100 % or less. The O content is preferably 0.0050 % or less. A lower limit of the O content is not particularly specified. However, in view of production technology constraints, the O content is preferably 0.0001 % or more.
  • [Al: 1.000 % or less]
  • Al exists as an oxide and decreases steel sheet ultimate deformability. Therefore, when Al content becomes excessive, achieving excellent toughness after paint baking becomes difficult. The Al content is therefore 1.000 % or less. The Al content is preferably 0.500 % or less. A lower limit of the Al content is not particularly specified. However, in view of production technology constraints, the Al content is preferably 0.001 % or more.
  • Basic chemical composition of the steel sheet according to an embodiment of the present disclosure is described above. The steel sheet according to an embodiment of the present disclosure has a chemical composition including the basic composition above, with the balance being Fe (iron) and inevitable impurity. Here, the steel sheet according to an embodiment of the present disclosure preferably has a chemical composition consisting of the basic composition above, with the balance being Fe and inevitable impurity. In addition to the basic components described above, the steel sheet according to an embodiment of the present disclosure may contain one or more elements selected from the following as optional additive elements, either alone or in combination.
    • Ti: 0.200 % or less,
    • Nb: 0.200 % or less,
    • V: 0.200 % or less,
    • Ta: 0.10 % or less,
    • W: 0.10 % or less,
    • B: 0.0100 % or less,
    • Cr: 1.00 % or less,
    • Mo: 1.00 % or less,
    • Ni: 1.00 % or less,
    • Co: 0.010 % or less,
    • Cu: 1.00 % or less,
    • Sn: 0.200 % or less,
    • Sb: 0.200 % or less,
    • Ca: 0.0100 % or less,
    • Mg: 0.0100 % or less,
    • REM: 0.0100 % or less,
    • Zr: 0.100 % or less,
    • Te: 0.100 % or less,
    • Hf: 0.10 % or less, and
    • Bi: 0.200 % or less.
  • The effects of the present disclosure are obtainable whenever content is equal to or less than the upper limit indicated above, and therefore there is no particular lower limit for the above optional additive elements. Further, when any of the above optional additional elements are included below a preferred lower limit described below, such an element is included as an inevitable impurity.
  • [Ti: 0.200 % or less, Nb: 0.200 % or less, V: 0.200 % or less]
  • When each of Ti, Nb, and V are 0.200 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Ti, Nb, and V are included, the content of each is preferably 0.200 % or less. The content of each of Ti, Nb, and V is respectively more preferably 0.100 % or less. A lower limit of the content of each of Ti, Nb, and V is not particularly specified. However, Ti, Nb, and V increase the strength of steel sheets by forming fine carbides, nitrides, or carbonitrides during hot rolling or annealing. Therefore, the content of each of Ti, Nb, and V is respectively preferably 0.001 % or more.
  • [Ta: 0.10 % or less, W: 0.10 % or less]
  • When each of Ta and W are 0.10 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Ta and W are included, the content of each is preferably 0.10 % or less. The content of each of Ta and W is respectively more preferably 0.08 % or less. A lower limit of the content of each of Ta and W is not particularly specified. However, Ta and W increase the strength of steel sheets by forming fine carbides, nitrides or carbonitrides during hot rolling or annealing. Therefore, the content of each of Ta and W is respectively preferably 0.01 % or more.
  • [B: 0.0100 % or less]
  • When B content is 0.0100 % or less, this element does not cause cracks inside the steel sheet during casting or hot rolling or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when B is included, the B content is preferably 0.0100 % or less. The B content is more preferably 0.0080 % or less. A lower limit of the B content is not particularly specified. However, B is an element that segregates at an austenite grain boundary during annealing and improves hardenability. The B content is therefore preferably 0.0003 % or more.
  • [Cr: 1.00 % or less, Mo: 1.00 % or less, Ni: 1.00 % or less]
  • When each of Cr, Mo, and Ni are 1.00 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Cr, Mo, and Ni are included, the content of each is preferably 1.00 % or less. The content of each of Cr, Mo, and Ni is respectively more preferably 0.80 % or less. A lower limit of the content of each of Cr, Mo, and Ni is not particularly specified. However, Cr, Mo, and Ni are elements that improve hardenability. Therefore, the content of each of Cr, Mo, and Ni is respectively preferably 0.01 % or more.
  • [Co: 0.010 % or less]
  • When Co is 0.010 % or less, this element does not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Co is included, the Co content is preferably 0.010 % or less. The Co content is more preferably 0.008 % or less. A lower limit of the Co content is not particularly specified. However, Co is an element that improves hardenability. The Co content is therefore preferably 0.001 % or more.
  • [Cu: 1.00 % or less]
  • When Cu is 1.00 % or less, this element does not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Cu is included, the Cu content is preferably 1.00 % or less. The Cu content is more preferably 0.80 % or less. A lower limit of the Cu content is not particularly specified. However, Cu is an element that improves hardenability. The Cu content is therefore preferably 0.01 % or more.
  • [Sn: 0.200 % or less]
  • When Sn content is 0.200 % or less, this element does not cause cracks inside the steel sheet during casting or hot rolling or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Sn is included, the Sn content is preferably 0.200 % or less. The Sn content is more preferably 0.100 % or less. A lower limit of the Sn content is not particularly specified. However, Sn is an element that improves hardenability and is generally also an element that improves corrosion resistance. The Sn content is therefore preferably 0.001 % or more.
  • [Sb: 0.200 % or less]
  • When Sb is 0.200 % or less, this element does not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Sb is included, the Sb content is preferably 0.200 % or less. The Sb content is more preferably 0.100 % or less. A lower limit of the Sb content is not particularly specified. However, Sb is an element that controls surface layer softening thickness and allows strength adjustment. The Sb content is therefore preferably 0.001 % or more.
  • [Ca: 0.0100 % or less, Mg: 0.0100 % or less, REM: 0.0100 % or less]
  • When each of Ca, Mg, and REM are 0.0100 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Ca, Mg, and REM are included, the content of each is preferably 0.0100 % or less. The content of each of Ca, Mg, and REM is respectively more preferably 0.0050 % or less. A lower limit of the content of each of Ca, Mg, and REM is not particularly specified. However, Ca, Mg, and REM are elements that spheroidize the shape of nitrides and sulfides and improve steel sheet ultimate deformability. Therefore, the content of each of Ca, Mg, and REM is respectively preferably 0.0005 % or more.
  • [Zr: 0.100 % or less, Te: 0.100 % or less]
  • When each of Zr and Te are 0.100 % or less, these elements do not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Zr and Te are included, the content of each is preferably 0.100 % or less. The content of each of Zr and Te is respectively more preferably 0.080 % or less. A lower limit of the content of each of Zr and Te is not particularly specified. However, Zr and Te are elements that spheroidize the shape of nitrides and sulfides and improve steel sheet ultimate deformability. Therefore, the content of each of Zr and Te is respectively preferably 0.001 % or more.
  • [Hf: 0.10 % or less]
  • When Hf is 0.10 % or less, this element does not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Hf is included, the Hf content is preferably 0.10 % or less. The Hf content is more preferably 0.08 % or less. A lower limit of the Hf content is not particularly specified. However, Hf is an element that spheroidizes the shape of nitrides and sulfides and improves steel sheet ultimate deformability. The Hf content is therefore preferably 0.01 % or more.
  • [Bi: 0.200 % or less]
  • When Bi is 0.200 % or less, this element does not cause large amounts of coarse precipitates or inclusions to form or cause steel sheet ultimate deformability to decrease. Therefore, a decrease in toughness after paint baking does not result. Therefore, when Bi is included, the Bi content is preferably 0.200 % or less. The Bi content is more preferably 0.100 % or less. A lower limit of the Bi content is not particularly specified. However, Bi is an element that reduces segregation. The Bi content is therefore preferably 0.001 % or more.
  • Elements other than those described above are Fe and inevitable impurity. Examples of inevitable impurity include Zn, Pb, As, Ge, Sr, and Cs. Such inevitable impurity is allowed to be included as long as a total amount is 0.100 % or less.
  • The following describes the microstructure of the steel sheet according to an embodiment of the present disclosure.
  • The microstructure of the steel sheet according to an embodiment of the present disclosure satisfies the following conditions:
    • area fraction of tempered martensite is 83 % or more,
    • area fraction of retained austenite is less than 3 %,
    • total area fraction of ferrite and bainitic ferrite is 5 % or more and less than 15 %,
    • 20° or greater grain boundary density in tempered martensite is 1.0 µm/µm2 or more, and
    • Expression (1) is satisfied.
  • The reasons for each of these limitations are described below. The area fraction of each phase is the area ratio occupied by each phase relative to the entire microstructure.
  • [Area fraction of tempered martensite: 83 % or more]
  • In the steel sheet according to an embodiment of the present disclosure, it is extremely important that the area fraction of tempered martensite is 83 % or more. That is, by making tempered martensite the main phase, in particular by making the area fraction 83 % or more, a TS of 1180 MPa or more is possible to achieve. The area fraction of tempered martensite is therefore 83 % or more. The area fraction of tempered martensite is preferably 85 % or more. The area fraction of tempered martensite is more preferably 87 % or more. An upper limit of the area fraction of tempered martensite is not specifically defined. The area fraction of tempered martensite is, for example, preferably less than 95 %. The area fraction of tempered martensite is more preferably 94 % or less. The area fraction of tempered martensite is even more preferably 93 % or less.
  • [Area fraction of retained austenite: less than 3 %]
  • In the steel sheet according to an embodiment of the present disclosure, it is extremely important that the area fraction of retained austenite is less than 3 %. That is, when the area fraction of retained austenite is 3 % or more, achieving excellent toughness after paint baking becomes difficult. One of the causes of decreased toughness after paint baking is that retained austenite transforms into deformation-induced martensite during processing, resulting in high-hardness martensite, which becomes an initiation point of a fracture. The area fraction of retained austenite is therefore less than 3 %. The area fraction of retained austenite is preferably 1 % or less. A lower limit of the area fraction of retained austenite is not specifically defined. The area fraction of retained austenite may be 0 %.
  • [Total area fraction of ferrite and bainitic ferrite: 5 % or more and less than 15 %]
  • In the steel sheet according to an embodiment of the present disclosure, it is extremely important that the total area fraction of ferrite and bainitic ferrite is more than 5 % and less than 15 %. That is, when the total area fraction of ferrite and bainitic ferrite is 15 % or more, achieving a TS of 1180 MPa or more becomes difficult. On the other hand, when the total area fraction of ferrite and bainitic ferrite is less than 5 %, it becomes difficult to achieve a high EL. Therefore, the total area fraction of ferrite and bainitic ferrite is 5 % or more and less than 15 %. The total area fraction of ferrite and bainitic ferrite is preferably 6 % or more. The total area fraction of ferrite and bainitic ferrite is more preferably 7 % or more. The total area fraction of ferrite and bainitic ferrite is preferably 14 % or less. The total area fraction of ferrite and bainitic ferrite is more preferably 13 % or less. Ferrite and bainitic ferrite may be included individually, or both may be included.
  • The area fraction of residual microstructure other than described above is preferably 5 % or less. Examples of residual microstructure include pearlite, fresh martensite, and acicular ferrite. These residual microstructures may be included as long as the content is 5 % or less, as they do not affect the properties. The area fraction of the residual microstructure may be 0 %.
  • Here, the area fraction of tempered martensite, as well as the total area fraction of ferrite and bainitic ferrite, is measured, for example, as follows.
  • A sample is cut from the steel sheet such that a thickness cross-section parallel to the rolling direction of the steel sheet (L-section) becomes an observation plane. The observation plane of the sample is then polished. The observation plane of the sample is then corroded with 3 vol% nital to reveal the microstructure. Then, a 1/4 sheet thickness position of the steel sheet (a position corresponding to 1/4 of the sheet thickness in the depth direction from a steel sheet surface) is observed at 2000× magnification by SEM for ten fields of view. In the observation images, tempered martensite has fine irregularities in the microstructure and contains carbides in the microstructure. Further, ferrite and bainitic ferrite have a flat microstructure in recessed portions and do not contain carbides. Then, for each field of view, the areas occupied by tempered martensite, as well as ferrite and bainitic ferrite, are determined. Next, for each field of view, the area occupied by tempered martensite, and the area occupied by ferrite and bainitic ferrite, are each divided by the total area of the observed field of view and multiplied by 100. Then, the average values of these are taken as the area fraction of tempered martensite and the total area fraction of ferrite and bainitic ferrite, respectively.
  • The microstructure of steel sheets is normally approximately vertically symmetrical in the thickness direction. Therefore, any one surface of the steel sheet (front or back) can be set as an initiation point of a thickness position (sheet thickness 0 position), such as the 1/4 sheet thickness position or a depth of 100 µm from the steel sheet surface.
  • Further, the area fraction of retained austenite is measured as follows.
  • That is, the steel sheet is mechanically ground to a depth of 1/4 - 0.1 mm so that the 1/4 sheet thickness position of the steel sheet becomes the observation position, and then further polished by 0.1 mm by chemical polishing. Using the polished surface as the observation plane, an integrated intensity of the diffraction peaks of bcc iron {200}, {211}, and {220} is compared to that of fcc iron (austenite) {200}, {220}, and {311} using Co Kα radiation with an X-ray diffractometer. A volume fraction of retained austenite is then calculated from the ratio of the integrated intensity of each plane. Then, assuming that the retained austenite is uniform in three dimensions, the volume fraction of the retained austenite is taken as the area fraction of retained austenite.
  • Further, the area fraction of the residual microstructure is determined by subtracting the area fraction of tempered martensite, the total area fraction of ferrite and bainitic ferrite, and the area fraction of retained austenite from 100 %. [Area fraction of residual microstructure (%)] = 100 - [area fraction of tempered martensite (%)] - [total area fraction of ferrite and bainitic ferrite (%)] - [area fraction of retained austenite (%)]
  • [20° or greater grain boundary density in tempered martensite: 1.0 µm/µm2 or more]
  • In the steel sheet according to an embodiment of the present disclosure, it is extremely important that the 20° or greater grain boundary density of tempered martensite is 1.0 µm/µm2 or more. Large-angle grain boundaries in tempered martensite, particularly 20° or greater grain boundaries in tempered martensite, become sites of carbon segregation during paint baking, helping prevent steel sheet fracture. As a result, fracture stress during tensile deformation decreases. Therefore, when 20° or greater grain boundary density in tempered martensite (hereinafter also referred to as large-angle grain boundary density of tempered martensite) is less than 1.0 µm/µm2, achieving excellent crash properties after paint baking becomes difficult. Therefore, the large-angle grain boundary density of tempered martensite is 1.0 µm/µm2 or more. The large-angle grain boundary density of tempered martensite is preferably 1.2 µm/µm2 or more. The large-angle grain boundary density of tempered martensite is more preferably 1.3 µm/µm2 or more. An upper limit of the large-angle grain boundary of tempered martensite is not specifically defined. For example, the large-angle grain boundary density of tempered martensite is preferably 3.0 µm/µm2 or less.
  • Here, the large-angle grain boundary density of tempered martensite is determined, for example, as follows.
  • A test piece for microstructure observation is collected from the steel sheet. The collected test piece is then polished by colloidal silica vibrational polishing so that the cross-section in the rolling direction (L-section) becomes the observation plane. The observation plane is mirror-finished. At the 1/4 sheet thickness position of the steel sheet (the position corresponding to 1/4 of the thickness in the depth direction from the surface of the steel sheet), electron backscatter diffraction (EBSD) measurement is performed to obtain local crystal orientation data. In the EBSD measurement, the step size is set to 0.10 µm, and the measurement area is 50 µm square (50 µm × 50 µm). Then, using the analysis software OIM Analysis 7, the obtained local crystal orientation data is analyzed. The analysis of the local crystal orientation data is executed for each of 10 fields of view at the 1/4 sheet thickness position of the steel sheet, and an average value is used. Further, prior to the analysis of the local crystal orientation data, a cleanup process is executed once using a grain dilatation function of the analysis software (grain tolerance angle: 5, minimum grain size: 2, single iteration: ON). Next, the 20° or greater grain boundaries in tempered martensite are displayed, and a total length of the 20° or greater grain boundaries in tempered martensite is determined. Then, by dividing the total length of the 20° or greater grain boundaries in tempered martensite by the area of the measurement region, the large-angle grain boundary density of tempered martensite is determined.
  • [KAM(S)/KAM(C) > 1.00]
  • In the steel sheet according to an embodiment of the present disclosure, it is extremely important that KAM(S)/KAM(C) exceeds 1.00. Here, KAM(S) is the KAM value at a depth of 100 µm from the steel sheet surface, and KAM(C) is the KAM value at the mid-thickness position of the steel sheet. As a result of various studies, the inventors discovered that changing the dislocation distribution state from the surface layer of the steel sheet to the interior is effective for improving crash properties after paint baking. In particular, by making KAM(S)/KAM(C) exceed 1.00, excellent crash properties after paint baking are obtainable. KAM(S)/KAM(C) is therefore more than 1.00. KAM(S)/KAM(C) is preferably 1.03 or more. An upper limit of KAM(S)/KAM(C) is not particularly defined. For example, KAM(S)/KAM(C) is preferably 1.110 or less.
  • Here, KAM(S) and KAM(C) can be determined, for example, as follows.
  • In the same manner as the measurement of the large-angle grain boundary density of tempered martensite, EBSD measurement is carried out, and the obtained local crystal orientation data is analyzed. The analysis of the local crystal orientation data is executed for 10 fields of view at a depth of 100 µm from the steel sheet surface and at the mid-thickness position of the steel sheet, and average values are used. Then, from the analysis results of the local crystal orientation data at the depth of 100 µm from the steel sheet surface and at the mid-thickness position of the steel sheet, a chart of the KAM values of the bcc phase for each position is created, and average values are used as KAM(S) and KAM(C), respectively.
  • Mechanical properties of the steel sheet according to an embodiment of the present disclosure are as described above.
  • Further, the steel sheet according to an embodiment of the present disclosure may include a coated or plated layer on a surface. The coated or plated layer may be on only one surface of the steel sheet or may be on both surfaces. The coated or plated layer is not particularly limited. As a coated or plated layer, a galvanized layer with Zn as the main component (Zn content of 50.0 mass% or more) is an example. Further, examples of galvanized layers include hot-dip galvanized layers, galvannealed layers, and electrogalvanized layers. A steel sheet that has a galvanized layer may also be referred to as a galvanized steel sheet. Further, a steel sheet that has a hot-dip galvanized layer, a galvannealed layer, or an electrogalvanized layer may also be referred to as a hot-dip galvanized steel sheet (GI), a galvannealed steel sheet (GA), or an electrogalvanized steel sheet (EG), respectively.
  • Coated or plated layers other than galvanized layers may include aluminum coated or plated layers and alloy coated or plated layers. As alloy coated or plated layers, examples include hot-dip zinc-aluminum-magnesium alloy coated layers and Zn-Ni electroplated alloy layers.
  • Further, coating weight per side of the coated or plated layer is not particularly limited. The coating weight per side of the coated or plated layer is preferably 20 g/m2 or more. The coating weight per side is preferably 80 g/m2 or less.
  • The thickness of the steel sheet according to an embodiment of the present disclosure is not particularly limited. The thickness of the steel sheet is preferably 0.50 mm or more. The thickness of the steel sheet is preferably 2.50 mm or less.
  • [2] Member
  • A member according to an embodiment of the present disclosure is described below.
  • The member according to an embodiment of the present disclosure is a member formed using the steel sheet described above as a material. For example, the material, the steel sheet, is subjected to at least one of a forming process or a joining process to make the member.
  • Here, the steel sheet described above has a TS of 1180 MPa or more, high EL, and also excellent toughness and crash properties after paint baking. Therefore, the member according to an embodiment of the present disclosure is particularly suitable for application as a material for automotive parts. This allows for improved fuel efficiency due to an automotive body weight decrease, which can greatly contribute to a decrease in CO2 emissions.
  • [3] Method of producing steel sheet
  • The following describes a method of producing a steel sheet according to an embodiment of the present disclosure.
  • The method of producing a steel sheet according to an embodiment of the present disclosure includes:
    • a preparation process of preparing a blank sheet having the chemical composition described above;
    • a heating process of heating the blank sheet under a set of conditions including an average heating rate in a temperature range from 700 °C to 750 °C of 5.0 °C/s or less, and
    • heating to an annealing temperature T1;
    • an annealing process of annealing the blank sheet under a set of conditions including the annealing temperature T1 being 750 °C or more and 850 °C or less, and
    • an annealing time t1 of 10 s or longer and 1000 s or shorter;
    • a bending process of applying bending once or more to the blank sheet using a roller that has a radius of 800 mm or less in a temperature range from the annealing temperature T1 to 700 °C;
    • a first cooling process of cooling the blank sheet under a set of conditions including an average cooling rate in a temperature range from 700 °C to 550 °C of 0.5 °C/s or more and less than 10.0 °C/s,
    • to a first cooling end temperature;
    • a second cooling process of cooling the blank sheet under a set of conditions including an average cooling rate in a temperature range from 300 °C to 100 °C of 300 °C/s or more, and
    • applying tension to the blank sheet in the temperature range from 300 °C to 100 °C of 5 MPa or more,
    • to a second cooling end temperature;
    • a tempering process of tempering the blank sheet under a set of conditions including a tempering temperature T2 of 100 °C or more and 400 °C or less, and
    • a tempering time t2 of 10 s or longer and 10,000 s or shorter; and
    • a straightening process of applying straightening to the blank sheet by leveling under a set of conditions including a straightening start temperature of 100 °C or less,
    • an entry side intermesh pressing amount of 4.0 mm or more and 10.0 mm or less,
    • a delivery intermesh pressing amount of 1.0 mm or more and 10.0 mm or less,
    • an entry side tension of 20 MPa or more and 500 MPa or less, and
    • a delivery tension of 25 MPa or more and 550 MPa or less.
  • Unless otherwise specified, each of the temperatures above refers to a surface temperature of the steel sheet. Further, the average heating rate and the average cooling rate are based on the surface temperature of the steel sheet, unless otherwise specified.
  • Preparation process
  • First, a blank sheet having the chemical composition described above is prepared. For example, a blank sheet can be prepared by hot rolling a steel slab into a hot-rolled steel sheet, then subjecting the hot-rolled steel sheet to optional pickling and heat treatment, and then cold rolling to obtain a cold-rolled steel sheet. The conditions of these processes are not particularly limited and may follow a conventional method.
  • For example, a method of smelting the steel slab (steel material) may be any known method, such as by use of a converter, an electric furnace, or the like. The steel slab is preferably smelted by continuous casting to help prevent macro-segregation.
  • Examples of hot rolling include methods such as rolling the steel slab after heating, direct rolling the steel slab after continuous casting without heating, and rolling the steel slab after applying a short heating treatment following continuous casting. Further, slab heating temperature, slab soaking duration, and coiling temperature in hot rolling are not particularly limited. The slab heating temperature is preferably 1100 °C or more. The slab heating temperature is preferably 1300 °C or less. The slab soaking duration is preferably 30 min or more. The slab soaking duration is preferably 250 min or less. The rolling finish temperature is preferably the Ar3 transformation temperature or more. The coiling temperature is preferably 350 °C or more. The coiling temperature is preferably 650 °C or less. The Ar3 transformation temperature is determined by the following expression. Ar3 transformation temperature (°C) = 868 - 396 × [%C] + 24.6 × [%Si] - 68.1 × [%Mn] - 36.1 × [%Ni] - 20.7 × [%Cu] - 24.8 × [%Cr]
  • Here, [%element symbol] in the above expression represents the content in mass% of the element in the chemical composition described above.
  • Pickling is capable of removing oxides from the surface of the hot-rolled steel sheet, and is preferably carried out to secure good chemical convertibility and coating quality in the final steel sheet product. Pickling may be carried out in one or more batches. Further, the hot-rolled steel sheet after pickling may be subjected to heat treatment.
  • The total rolling reduction in the cold rolling is preferably 30 % or more. The total rolling reduction in the cold rolling is preferably 80 % or less. The defined effect can be obtained without limiting the number of rolling passes or the rolling reduction for each pass.
  • Heating process
  • Next, the blank sheet prepared in the preparation process is heated to the annealing temperature T1 under a set of conditions including an average heating rate of 5.0 °C/s or less in the temperature range of 700 °C to 750 °C. The annealing temperature T1 is explained in the annealing process described later.
  • [Average heating rate in temperature range of 700 °C to 750 °C: 5.0 °C/s or less]
  • The inventors have carried out intensive studies and found that the average heating rate in the temperature range of 700 °C to 750 °C (hereinafter also referred to simply as average heating rate) affects the density of large-angle grain boundaries of tempered martensite. That is, by setting the average heating rate to 5.0 °C/s or less, the dissolution of carbides is promoted. As a result, prior austenite grain boundaries are refined, and the number of 20° or greater grain boundaries after martensitic transformation increases. Therefore, the density of large-angle grain boundaries of tempered martensite in the final steel sheet product also increases, improving crash properties after paint baking. Accordingly, the average heating rate is 5.0 °C/s or less. The average heating rate is preferably 3.0 °C/s or less. A lower limit of the average heating rate is not specifically defined. For example, the average heating rate is preferably 0.1 °C/s or more.
  • Annealing process
  • Next, the blank sheet is annealed under a set of conditions including the annealing temperature T1 being 750 °C or more and 850 °C or less, and annealing time t1 being 10 s or longer and 1000 s or shorter.
  • [Annealing temperature T1: 750 °C or more and 850 °C or less]
  • When the annealing temperature T1 is less than 750 °C, the total area fraction of ferrite and bainitic ferrite becomes 15 % or more, and achieving a TS of 1180 MPa or more becomes difficult. On the other hand, when the annealing temperature T1 exceeds 850 °C, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, making it difficult to achieve a high EL. The annealing temperature T1 is therefore 750 °C or more and 850 °C or less. The annealing temperature T1 is preferably 760 °C or more. The annealing temperature T1 is more preferably 770 °C or more. The annealing temperature T1 is preferably 840 °C or less. The annealing temperature T1 is more preferably 830 °C or less. The annealing temperature referred to here is the holding temperature during the annealing process. Further, the annealing temperature may remain constant during holding. Further, the annealing temperature is the temperature range of 750 °C or more and 850 °C or less, and when temperature fluctuation is within ±10 °C of the set temperature, the annealing temperature does not have to be constant during holding.
  • [Annealing time t1: 10 s or longer and 1000 s or shorter]
  • When the annealing time t1 is less than 10 s, the total area fraction of ferrite and bainitic ferrite becomes 15 % or more, and achieving a TS of 1180 MPa or more becomes difficult. On the other hand, when the annealing time t1 exceeds 1000 s, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, making it difficult to achieve a high EL. The annealing time t1 is therefore 10 s or longer and 1000 s or shorter. The annealing time t1 is preferably 30 s or longer. The annealing time t1 is preferably 800 s or shorter. The annealing time t1 referred to here is the holding time at the annealing temperature T1.
  • Bending process
  • Next, the blank sheet is subjected to bending once or more using a roller that has a radius of 800 mm or less in the temperature range from the annealing temperature T1 to 700 °C.
  • [Number of times bending using a roller that has a radius of 800 mm or less in the temperature range from the annealing temperature T1 to 700 °C: once or more]
  • As a result of intensive studies, the inventors found that carrying out bending in the temperature range from the annealing temperature T1 to 700 °C (hereinafter also referred to as bending temperature range) affects the large-angle grain boundary density of tempered martensite. In particular, carrying out bending using a roller that has a radius of 800 mm or less in the bending temperature range promotes martensitic transformation nucleation. As a result, martensite is refined, and 20° or greater grain boundaries after martensitic transformation increase. Therefore, the density of large-angle grain boundaries of tempered martensite in the final steel sheet product also increases, improving crash properties after paint baking. Accordingly, the number of times bending using a roller that has a radius of 800 mm or less in the bending temperature range (hereinafter also referred to as bending count) is set to be once or more.
  • The radius of the roller used for bending is preferably 600 mm or less. A lower limit of the radius of the roller used for bending is not particularly restricted. For example, the radius of the roller used for bending is preferably 100 mm or more.
  • Further, the number of bends may be one or more. The number of bends is preferably two or more. An upper limit of the number of bends is not specifically defined. For example, the number of bends is preferably 15 or fewer. The bending may be carried out by bending in one direction with a roller and then bending back the same amount in the opposite direction. In such a case, the number of bends is counted as two (one for bending and one for bending back). Further, the bending angle is preferably 80° or more. The bending angle is preferably 110° or less. This results in a greater effect of promoting martensitic transformation nucleation. The bending angle is the angle (acute angle) formed between the sheet passing direction of the steel sheet on the roller entry side and the sheet passing direction of the steel sheet on the roller delivery side.
  • When bending using a roller that has a radius of 800 mm or less is carried out at least once in the bending temperature range, additional bending that does not satisfy the described conditions may be carried out.
  • First cooling process
  • Next, the blank sheet is cooled to a first cooling end temperature under a set of conditions including an average cooling rate of 0.5 °C/s or more and less than 10.0 °C/s in a temperature range from 700 °C to 550 °C.
  • [Average cooling rate in temperature range from 700 °C to 550 °C: 0.5 °C/s or more and less than 10.0 °C/s]
  • When the average cooling rate in the temperature range from 700 °C to 550 °C (hereinafter also referred to as first average cooling rate) is 10.0 °C/s or more, the total area fraction of ferrite and bainitic ferrite becomes less than 5 %, and achieving a high EL becomes difficult. On the other hand, when the first average cooling rate is less than 0.5 °C/s, the total area fraction of ferrite and bainitic ferrite becomes 15 % or more, and achieving a TS of 1180 MPa or more becomes difficult. The first average cooling rate is therefore 0.5 °C/s or more and less than 10.0 °C/s. The first average cooling rate is preferably 1.0 °C/s or more. The first average cooling rate is preferably 8.0 °C/s or less.
  • The first cooling end temperature may be, for example, from 550 °C to 300 °C. Further, a coating or plating treatment may be applied to the blank sheet between the first cooling process and the second cooling process described later. Details about the coating or plating treatment are described later.
  • Second cooling process
  • Next, the blank sheet is cooled to the second cooling end temperature under a set of conditions including an average cooling rate of 300 °C/s or more in a temperature range from 300 °C to 100 °C, and a tension of 5 MPa or more applied to the blank sheet in the temperature range from 300 °C to 100 °C.
  • [Average cooling rate in temperature range from 300 °C to 100 °C: 300 °C/s or more]
  • When the average cooling rate in the temperature range from 300 °C to 100 °C (hereinafter also referred to as second average cooling rate) is less than 300 °C/s, the area fraction of retained austenite becomes 3 % or more, and achieving excellent toughness after paint baking becomes difficult. The second average cooling rate is therefore 300 °C/s or more. The second average cooling rate is preferably 800 °C/s or more. An upper limit of the second average cooling rate is not specifically defined. For example, the second average cooling rate is preferably 2000 °C/s or less.
  • [Tension applied to blank sheet in temperature range from 300 °C to 100 °C: 5 MPa or more]
  • As a result of intensive studies, the inventors found that applied tension to the blank sheet during cooling in the temperature range from 300 °C to 100 °C affects the large-angle grain boundary density of tempered martensite. In particular, when the tension applied to the blank sheet in the temperature range from 300 °C to 100 °C (hereinafter also referred to simply as applied tension) is 5 MPa or more, martensitic transformation is promoted. As a result, martensite is refined, and 20° or greater grain boundaries after martensitic transformation increase. Therefore, the density of large-angle grain boundaries of tempered martensite in the final steel sheet product also increases, improving crash properties after paint baking. Accordingly, the applied tension is 5 MPa or more. The applied tension is preferably 10 MPa or more. An upper limit of the applied tension is not specifically defined. For example, the applied tension is preferably 100 MPa or less.
  • Further, the second cooling end temperature may be, for example, less than 100 °C. The second cooling end temperature may be, for example, around room temperature.
  • The bending in the bending process described above increases the number of nucleation sites, which are initiation points of martensitic transformation. On the other hand, the application of tension in the second cooling process promotes the martensitic transformation itself. That is, the effects obtained from both are different.
  • Tempering process
  • Next, the blank sheet is tempered under a set of conditions including the tempering temperature T2 being 100 °C or more and 400 °C or less, and tempering time t2 being 10 s or longer and 10,000 s or shorter.
  • [Tempering temperature T2: 100 °C or more and 400 °C or less]
  • Tempered martensite is formed by tempering treatment, where martensite is tempered. Here, when the tempering temperature T2 is less than 100 °C, martensite is not sufficiently tempered, resulting in a microstructure mainly composed of quenched martensite. In such a microstructure mainly composed of quenched martensite, excellent toughness after paint baking cannot be obtained. On the other hand, when the tempering temperature T2 exceeds 400 °C, tempering of martensite progresses excessively, and achieving a TS of 1180 MPa or more becomes difficult. The tempering temperature T2 is therefore 100 °C or more and 400 °C or less. The tempering temperature T2 is preferably 150 °C or more. The tempering temperature T2 is preferably 350 °C or less. The tempering temperature referred to here is the holding temperature during the tempering process. The tempering temperature may be constant during holding. Further, the tempering temperature is in the range from 100 °C or more to 400 °C or less, and when temperature fluctuation is within ±10 °C of the set temperature, the tempering temperature does not have to be constant during holding.
  • [Tempering time t2: 10 s or longer and 10,000 s or shorter]
  • As mentioned above, tempered martensite is formed by tempering treatment, where martensite is tempered. Here, when the tempering time t2 is shorter than 10 s, martensite is not sufficiently tempered, resulting in a microstructure mainly composed of quenched martensite. In such a microstructure mainly composed of quenched martensite, excellent toughness after paint baking cannot be obtained. On the other hand, when the tempering time t2 exceeds 10,000 s, tempering of martensite progresses excessively, and achieving a TS of 1180 MPa or more becomes difficult. Accordingly, the tempering time t2 is 10 s or longer and 10,000 s or shorter. The tempering time t2 is preferably 50 s or longer. The tempering time t2 is preferably 5000 s or shorter. Here, the tempering time t2 refers to the holding time at the tempering temperature T2.
  • The cooling after tempering is not specifically defined. For example, it is sufficient to cool by any method according to a conventional method. The cooling end temperature after tempering may be, for example, around room temperature. Further, a coating or plating treatment may be applied to the blank sheet between the tempering process and the straightening process described below. Details about the coating or plating treatment are described later.
  • Straightening process
  • Next, the blank sheet is subjected to straightening by leveling (using a leveler). At this time, satisfying the following conditions is extremely important in the method of producing the steel sheet according to an embodiment of the present disclosure.
    • Straightening start temperature of 100 °C or less,
    • an entry side intermesh pressing amount of 4.0 mm or more and 10.0 mm or less,
    • a delivery intermesh pressing amount of 1.0 mm or more and 10.0 mm or less,
    • an entry side tension of 20 MPa or more and 500 MPa or less, and
    • a delivery tension of 25 MPa or more and 550 MPa or less.
    [Straightening start temperature: 100 °C or less]
  • When the straightening start temperature exceeds 100 °C, the steel sheet becomes soft. As a result, the amount of strain introduced into the surface layer and the center of the steel sheet by leveling changes, and KAM(S)/KAM(C) becomes 1.00 or less. Therefore, crash properties after paint baking are decreased. The straightening start temperature is therefore 100 °C or less. The straightening start temperature is preferably 80 °C or less. A lower limit of the straightening start temperature is not specifically defined. For example, the straightening start temperature is preferably -10 °C or more.
  • [Entry side intermesh pressing amount: 4.0 mm or more and 10.0 mm or less]
  • When the entry side intermesh pressing amount is less than 4.0 mm, the amount of processing is insufficient. As a result, KAM(S)/KAM(C) becomes 1.00 or less, and the crash properties after paint baking decrease. An upper limit of the entry side intermesh pressing amount is 10.0 mm or less in view of production technology constraints. The entry side intermesh pressing amount is therefore 4.0 mm or more and 10.0 mm or less. The entry side intermesh pressing amount is preferably 5.0 mm or more.
  • [Delivery intermesh pressing amount: 1.0 mm or more and 10.0 mm or less]
  • When the delivery intermesh pressing amount is less than 1.0 mm, the amount of processing is insufficient. As a result, KAM(S)/KAM(C) becomes 1.00 or less, and the crash properties after paint baking decrease. An upper limit of the delivery intermesh pressing amount is 10.0 mm or less in view of production technology constraints. The delivery intermesh pressing amount is therefore 1.0 mm or more and 10.0 mm or less.
  • Here, the entry side intermesh pressing amount, as indicated in FIG. 1, refers to the pressing amount of the second roller from the entry side (roller 2 in FIG. 1) against the steel sheet plane (the surface of the steel sheet where roller 2 is disposed) in leveling. Further, the delivery intermesh pressing amount refers to the pressing amount of the second roller from the delivery side (roller 8 in FIG. 1) against the steel sheet plane (the surface of the steel sheet where roller 8 is disposed) in leveling. The number of rollers in the leveling (leveler) is not particularly limited. For example, five or more rollers is preferred.
  • [Entry side tension: 20 MPa or more and 500 MPa or less]
  • When the entry side tension is less than 20 MPa, the amount of processing is insufficient. Therefore, KAM(S)/KAM(C) becomes 1.00 or less, and the crash properties after paint baking decrease. The upper limit of the entry side tension is 500 MPa in view of production technology constraints. Accordingly, the entry side tension is 20 MPa or more and 500 MPa or less. The entry side tension is preferably 100 MPa or more.
  • [Delivery tension: 25 MPa or more and 550 MPa or less]
  • Due to leveler apparatus constraints, the delivery tension is higher than the entry side tension. Here, when the delivery intermesh pressing amount is less than 25 MPa, the amount of processing is insufficient. Therefore, KAM(S)/KAM(C) becomes 1.00 or less, and the crash properties after paint baking decrease. The upper limit of the delivery tension is 550 MPa or less in view of production technology constraints. Accordingly, the delivery tension is 25 MPa or more and 550 MPa or less. The delivery tension is preferably 100 MPa or more.
  • Coating or plating process
  • Further, optionally, the steel sheet may be subjected to coating or plating treatment. Coating or plating treatment is not particularly limited. Examples of coating or plating treatment include galvanizing treatment such as hot-dip galvanizing treatment, galvannealing treatment, and electrogalvanization treatment. Other than galvanizing treatment, examples of coating or plating treatment include aluminum coating or plating treatment and alloy coating or plating treatment. Examples of alloy coating or plating treatment include hot-dip zinc-aluminum-magnesium alloy coating treatment and Zn-Ni electro-alloy plating treatment. Treatment conditions may follow conventional methods. As mentioned above, the coating or plating treatment is preferably carried out between the first cooling process and the second cooling process, or between the tempering process and the straightening process. For example, hot-dip galvanizing treatment or galvannealing treatment is preferably carried out between the first cooling process and the second cooling process. Further, electrogalvanization treatment or Zn-Ni electro-alloy plating treatment is preferably carried out between the tempering process and the straightening process.
  • In the case of hot-dip galvanizing treatment and galvannealing treatment, from the perspective of productivity, the series of treatments including the heating process, the annealing process, and the coating or plating treatment process is preferably carried out on a continuous galvanizing line (CGL). After the hot-dip galvanizing, wiping may be carried out for adjusting the coating amount.
  • Conditions other than those described above are not particularly limited, and a conventional method may be used. According to the method of producing the steel sheet according to an embodiment of the present disclosure described above, a steel sheet is obtainable that has a TS of 1180 MPa or more, high EL, and also excellent toughness and crash properties after paint baking. The obtained steel sheet may be suitably used as a material for automotive parts, for example.
  • [4] Method of producing member
  • The following describes a method of producing a member according to an embodiment of the present disclosure.
  • The method of producing a member according to an embodiment of the present disclosure includes process of at least one of forming or joining the steel sheet described above to make the member.
  • Here, a forming method is not particularly limited, and a typical processing method such as press forming may be used, for example. Further, a joining method is also not particularly limited, and for example, typical welding such as spot welding, laser welding, arc welding, and the like, rivet joining, swaging joining, and the like may be used. Forming and joining conditions are not particularly limited and may follow a conventional method.
  • EXAMPLES
  • Steel having the chemical compositions listed in Table 1 (the balance being Fe and inevitable impurity) was melted in a converter and made into steel slabs by a continuous casting method. The steel slabs were then heated. The steel slabs were then hot rolled to produce hot-rolled steel sheets. Pickling treatment was then carried out on the hot-rolled steel sheets. The hot-rolled steel sheets were then subjected to cold rolling to obtain cold-rolled steel sheets. In this way, blank sheets were prepared. The prepared blank sheets then underwent the heating process, the annealing process, the bending process, the first cooling process, the second cooling process, the tempering process, and the straightening process under conditions including the conditions listed in Table 2 to obtain final product steel sheets (thickness: 0.6 mm to 2.2 mm). The first cooling end temperature in each case was set to 550 °C to 300 °C. Both the second cooling end temperature and the cooling end temperature after tempering were set to room temperature. The bending angle in the bending was set to 80° to 110°. Further, some of the steel sheets (those listed as GI, GA, and EG in Table 2) were subjected to coating or plating treatment. Among these, for those listed as GI and GA in Table 2, coating treatment was carried out between the first cooling process and the second cooling process. For those listed as EG in Table 2, plating treatment was carried out between the tempering process and the straightening process. Conditions not specified were followed according to conventional methods.
  • Using the obtained steel sheets, the area fraction of tempered martensite, the area fraction of retained austenite, the total area fraction of ferrite and bainitic ferrite, the large-angle grain boundary density of tempered martensite, and KAM(S)/KAM(C) were determined in the manner described above. Results are listed in Table 3.
  • Further, each evaluation was carried out according to the following procedure. The evaluation results are listed in Table 3.
  • (Evaluation of TS)
  • From each obtained steel sheet, a JIS No. 5 test piece (gauge length: 50 mm, parallel portion width: 25 mm) was taken so that the direction perpendicular to the rolling direction of the steel sheet was the longitudinal direction of the test piece. Next, a tensile test was conducted according to JIS Z 2241:2022 using the test piece, and TS and EL were measured. The crosshead speed was set to 1.67 × 10-1 mm/s. Evaluation was based on the following criteria.
    • Good (pass, very good): TS was 1180 MPa or more
    • Poor (fail): TS was less than 1180 MPa
    (Evaluation of EL)
  • The EL measured in the above tensile tests was evaluated according to the following criteria.
    • Good (pass, very good): EL was 10 % or more
    • Poor (fail): EL was less than 10 %
    (Evaluation of toughness after paint baking)
  • For each obtained steel sheet, a plurality of sheets were stacked and fastened with bolts. Next, after confirming that there were no gaps between the steel sheets, a V-notch having a depth of 2 mm was applied to the stacked steel sheets, and a stacked Charpy test piece (hereinafter also referred to simply as the test piece) was prepared. The number of stacked steel sheets was set to the number that most closely approaches a thickness of 10 mm for the test piece (when there were two numbers that were closest to 10 mm, the smaller number was chosen). For example, when the thickness of the steel sheet was 1.2 mm, eight sheets of the steel sheet were stacked together. That is, the thickness of the test piece was 9.6 mm. Further, the test piece was prepared so that the sheet transverse direction of the steel sheet (direction perpendicular to the rolling direction) was the longitudinal direction of the test piece. The prepared test piece was then subjected to aging treatment at a treatment temperature of 170 °C for a treatment time of 20 min. Using the test piece that was subjected to the aging treatment, a Charpy impact test was carried out in a test temperature range of -120 °C to +120 °C. From the obtained percent brittle fracture, a transition curve was determined, and the temperature at which the percent brittle fracture reached 50 % was defined as the brittle-ductile transition temperature. Based on the following criteria, the toughness after paint baking was evaluated. Other than the above conditions, JIS Z 2242:2018 was followed.
    • Excellent (pass, particularly good): the brittle-ductile transition temperature after aging treatment was -60 °C or lower.
    • Good (pass, very good): the brittle-ductile transition temperature after aging treatment was -40 °C or lower (excluding Excellent results).
    • Poor (fail): the brittle-ductile transition temperature after aging treatment was higher than -40 °C.
    (Crash properties after paint baking)
  • The obtained steel sheets were each subjected to aging treatment at a treatment temperature of 170 °C for a treatment time of 20 min. From each steel sheet subjected to aging treatment, a JIS No. 5 test piece (gauge length: 50 mm, parallel portion width: 25 mm) was taken so that the direction perpendicular to the rolling direction of the steel sheet was the longitudinal direction of the test piece. Then, using the test piece, a tensile test was carried out according to JIS Z 2241:2022 in the same manner as in the TS evaluation described above, measuring the TS, yield stress (YS), and fracture stress after aging treatment. Based on the following criteria, the crash properties after paint baking were then evaluated.
    • Good (pass, very good): the YR after aging treatment was 0.85 or more, and the fracture stress ratio after aging treatment was 0.90 or less.
    • Poor (fail): at least one of the YR after aging treatment being 0.85 or more and the fracture stress ratio after aging treatment being 0.90 or less was not satisfied.
  • The YR and fracture stress ratio after aging treatment are determined by the following expressions, respectively. [YR after aging treatment] = [YS after aging treatment] / [TS after aging treatment] [Fracture stress ratio after aging treatment] = [fracture stress after aging treatment] / [TS after aging treatment]
  • Further, the fracture stress is the stress at the fracture point in the tensile test (the stress applied when the test piece fractures).
  • [Table 1]
  • Table 1
    Steel sample ID Chemical composition (mass%) Remarks
    C Si Mn P S N O Al Ti Nb B Cu Other
    A 0.245 0.251 1.25 0.008 0.0010 0.0042 0.0049 0.049 Conforming steel
    B 0.232 0.296 1.28 0.008 0.0008 0.0057 0.0041 0.042 Conforming steel
    C 0.212 0.235 1.16 0.006 0.0010 0.0051 0.0068 0.022 Conforming steel
    D 0.201 0.289 1.89 0.008 0.0009 0.0018 0.0042 0.056 Conforming steel
    E 0.217 0.252 1.53 0.010 0.0009 0.0034 0.0052 0.032 Conforming steel
    F 0.037 0.162 1.52 0.010 0.0010 0.0063 0.0025 0.045 Conforming steel
    G 0.024 0.299 1.01 0.012 0.0007 0.0010 0.0014 0.045 Comparative steel
    H 0.479 0.136 1.26 0.012 0.0006 0.0067 0.0057 0.010 Conforming steel
    I 0.505 0.220 1.19 0.013 0.0010 0.0052 0.0033 0.030 Comparative steel
    J 0.234 0.011 1.23 0.009 0.0009 0.0018 0.0019 0.037 Conforming steel
    K 0.200 0.005 1.38 0.009 0.0010 0.0049 0.0070 0.036 Comparative steel
    L 0.217 2.376 1.24 0.010 0.0009 0.0022 0.0065 0.020 Conforming steel
    M 0.240 2.580 1.64 0.010 0.0012 0.0067 0.0051 0.059 Comparative steel
    N 0.203 0.218 0.15 0.007 0.0011 0.0032 0.0016 0.030 Conforming steel
    Q 0.208 0.243 0.07 0.008 0.0013 0.0070 0.0015 0.024 Comparative steel
    P 0.242 0.233 4.92 0.006 0.0012 0.0055 0.0019 0.019 Conforming steel
    Q 0.203 0.122 5.16 0.013 0.0007 0.0040 0.0042 0.048 Comparative steel
    R 0.221 0.207 1.62 0.097 0.0013 0.0036 0.0044 0.028 Conforming steel
    S 0.240 0.289 1.92 0.109 0.0007 0.0019 0.0021 0.036 Comparative steel
    T 0.249 0.171 1.39 0.013 0.0192 0.0039 0.0047 0.029 Conforming steel
    U 0.220 0.164 1.94 0.011 0.0203 0.0016 0.0018 0.048 Comparative steel
    V 0.223 0.223 1.50 0.013 0.0008 0.0038 0.0061 0.924 Conforming steel
    W 0.220 0.166 1.17 0.009 0.0011 0.0022 0.0031 1.049 Comparative steel
    X 0.206 0.192 1.03 0.007 0.0015 0.0094 0.0054 0.021 Conforming steel
    Y 0.247 0.168 1.63 0.010 0.0009 0.0111 0.0058 0.050 Comparative steel
    Z 0.212 0.101 1.81 0.011 0.0011 0.0045 0.0088 0.047 Conforming steel
    AA 0.236 0.221 1.11 0.012 0.0010 0.0041 0.0112 0.045 Comparative steel
    AB 0.207 0.201 1.40 0.010 0.0012 0.0019 0.0048 0.025 Conforming steel
    AC 0.224 0.209 1.72 0.011 0.0013 0.0037 0.0014 0.039 0.001 Conforming steel
    AD 0.246 0.278 1.09 0.009 0.0005 0.0044 0.0063 0.019 0.199 Conforming steel
    AE 0.234 0.256 1.75 0.010 0.0007 0.0029 0.0052 0.047 0.214 Comparative steel
    AF 0.249 0.241 1.21 0.013 0.0014 0.0027 0.0024 0.018 0.0004 Conforming steel
    AG 0.221 0.112 1.95 0.007 0.0009 0.0041 0.0013 0.031 0.0085 Conforming steel
    AH 0.237 0.210 1.09 0.008 0.0014 0.0059 0.0041 0.054 0.0120 Comparative steel
    AI 0.201 0.154 1.35 0.009 0.0011 0.0044 0.0030 0.056 0.002 Conforming steel
    AJ 0.214 0.249 1.06 0.009 0.0013 0.0042 0.0022 0.012 0.196 Conforming steel
    AK 0.242 0.201 1.62 0.012 0.0012 0.0065 0.0037 0.022 0.209 Comparative steel
    AL 0.236 0.155 1.48 0.008 0.0010 0.0052 0.0058 0.060 0.01 Conforming steel
    AM 0.240 0.161 1.48 0.012 0.0014 0.0029 0.0039 0.011 0.99 Conforming steel
    AN 0.235 0.103 1.95 0.009 0.0011 0.0027 0.0035 0.053 1.15 Comparative steel
    AO 0.225 0.210 1.32 0.012 0.0009 0.0033 0.0056 0.013 V:0.049 Conforming steel
    AP 0.227 0.236 1.88 0.006 0.0010 0.0033 0.0021 0.037 Ta:0.06 Conforming steel
    AQ 0.203 0.290 1.80 0.013 0.0011 0.0026 0.0060 0.014 W:0.05 Conforming steel
    AR 0.219 0.173 1.41 0.006 0.0010 0.0066 0.0023 0.021 Cr:0.32 Conforming steel
    AS 0.223 0.262 1.87 0.012 0.0012 0.0056 0.0068 0.052 Mo:0.85 Conforming steel
    AT 0.244 0.246 1.19 0.009 0.0007 0.0066 0.0036 0.056 Co:0.007 Conforming steel
    AU 0.202 0.141 1.33 0.010 0.0010 0.0029 0.0057 0.054 Ni:0.02 Conforming steel
    AV 0.225 0.184 1.39 0.012 0.0010 0.0036 0.0018 0.033 Sn:0.012 Conforming steel
    AW 0.249 0.233 1.13 0.014 0.0013 0.0046 0.0014 0.034 Sb:0.058 Conforming steel
    AX 0.235 0.157 1.23 0.010 0.0009 0.0012 0.0034 0.017 Ca:0.0088 Conforming steel
    AY 0.231 0.258 1.70 0.014 0.0012 0.0020 0.0039 0.044 Mg:0.0016 Conforming steel
    AZ 0.209 0.252 1.82 0.015 0.0009 0.0058 0.0061 0.038 Zr:0.067 Conforming steel
    BA 0.220 0.211 1.45 0.006 0.0009 0.0040 0.0049 0.056 Te:0.024 Conforming steel
    BB 0.237 0.192 1.76 0.013 0.0013 0.0035 0.0035 0.026 Hf:0.07 Conforming steel
    BC 0.235 0.113 1.82 0.006 0.0009 0.0035 0.0022 0.029 REM0.0077 Conforming steel
    BD 0.237 0.214 1.30 0.008 0.0008 0.0021 0.0043 0.034 Bi:0.149 Conforming steel
    BE 0.231 0.236 1.19 0.014 0.0011 0.0022 0.0014 0.057 Zn 0.090 Conforming steel
    BF 0.216 0.134 1.62 0.007 0.0007 0.0031 0.0052 0.013 Pb:0.052 Conforming steel
    BG 0.208 0.220 1.37 0.012 0.0013 0.0032 0.0060 0.053 As:0.028 Conforming steel
    BH 0.214 0.185 1.47 0.010 0.0012 0.0068 0.0012 0.038 Ge:0.033 Conforming steel
    BI 0.209 0.268 1.89 0.006 0.0013 0.0052 0.0010 0.028 Sr:0.011 Conforming steel
    BJ 0.226 0.189 1.38 0.014 0.0008 0.0020 0.0053 0.044 Cs:0.025 Conforming steel
    BK 0.239 0.295 1.82 0.006 0.0011 0.0059 0.0046 0.052 Conforming steel
    BL 0.248 0.276 1.58 0.014 0.0007 0.0035 0.0055 0.014 Conforming steel
    BM 0.227 0.259 1.94 0.008 0.0008 0.0041 0.0012 0.030 Conforming steel
    BN 0.234 0.142 1.20 0.007 0.0015 0.0039 0.0048 0.053 Conforming steel
    BO 0.243 0.291 1.41 0.012 0.0010 0.0025 0.0070 0.046 Conforming steel
    Underlined: indicates value outside scope of present disclosure.
  • [Table 2]
  • Table 2
    No. Steel sample ID Heating process Annealing process Bending process First cooling process Second cooling process Tempering process Straightening process Type* Remarks
    Average heating rate (°C/S ) Annealing temp. T1 (°C) Annealing time t1 (s) Number of bends (times) First average cooling rate (° C/s) Second average cooling rate (°C/s) Applied tension (MPa) Tempering temp. T2 (°C) Tempering time t2 (s) Straightening start temp. (°C) Entry side intermesh pressing amount (mm) Delivery intermesh pressing amount (mm) Entry side tension (MPa) Delivery tension (MPa)
    1 A 0.8 791 189 3 4.8 906 11 190 732 34 6.7 1.5 168 177 CR Example
    2 B 0.6 793 193 3 3.4 919 14 185 688 40 6.9 1.4 201 209 CR Example
    3 B 0.1 800 165 4 1.6 964 14 182 572 26 7.0 1.7 224 232 CR Example
    4 B 0.7 799 61 3 1.1 807 16 178 676 29 6.1 1.4 201 209 CR Example
    5 B 4.5 802 198 2 2.6 966 13 199 871 32 6.1 1.3 228 237 CR Example
    6 B 5.2 797 151 3 4.9 854 17 185 502 32 6.9 1.7 177 184 CR Comparative Example
    7 B 0.4 758 66 4 2.4 889 14 207 789 29 6.3 1.8 233 240 CR Example
    8 B 0.4 744 94 4 2.7 813 13 209 765 20 6.5 2.0 245 253 CR Comparative Example
    9 B 0.4 846 111 4 2.7 994 11 183 947 40 7.1 1.4 174 181 CR Example
    10 B 0.9 859 67 2 4.0 808 16 192 822 32 7.7 1.7 257 264 CR Comparative Example
    11 B 0.8 801 15 3 2.0 848 13 181 803 29 7.9 1.7 184 192 CR Example
    12 B 0.2 798 2 2 3.4 948 19 172 566 39 7.7 1.7 271 280 CR Comparative Example
    13 B 0.5 795 984 4 1.4 998 12 210 860 29 7.2 2.0 167 173 CR Example
    14 B 0.9 810 1054 3 2.0 928 12 199 590 33 6.4 1.7 244 252 CR Comparative Example
    15 B 0.3 805 199 1 3.0 883 20 210 988 37 6.3 1.2 282 292 CR Example
    16 B 09 797 117 0 44 820 18 193 831 32 73 2.0 272 279 CR Comparative Example
    17 B 0.8 805 110 0 3.8 954 18 190 992 31 7.7 1.5 284 290 CR Comparative Example
    18 B 0.3 790 133 9 2.5 977 10 208 939 40 7.9 1.8 236 245 CR Example
    19 B 0.7 808 103 4 0.6 807 18 202 669 32 6.9 1.5 251 260 CR Example
    20 B 0.4 794 70 5 0.3 867 16 199 681 21 6.2 1.1 252 258 CR Comparative Example
    21 B 0.4 791 132 2 8.4 899 11 175 804 38 7.1 1.1 263 273 CR Example
    22 B 0.9 793 69 4 10.5 934 11 181 986 24 6.5 1.9 249 259 CR Comparative Example
    23 B 0.5 790 139 4 3.8 305 19 185 692 24 6.5 1.4 197 205 CR Example
    24 B 0.3 810 164 3 3.2 254 12 195 507 26 6.0 1.8 160 167 CR Comparative Example
    25 B 0.6 794 179 5 3.0 1992 12 189 968 22 6.1 1.8 269 277 CR Example
    26 B 0.3 791 78 3 2.3 978 17 178 523 29 6.0 1.5 209 215 CR Example
    27 B 0.6 794 87 3 3.4 837 6 176 812 39 6.2 1.8 159 165 CR Example
    28 B 0.8 796 70 4 2.7 964 2 176 777 21 6.5 1.9 183 192 CR Comparative Example
    29 B 0.9 806 71 4 1.8 984 44 189 736 21 6.9 1.6 252 257 CR Example
    30 B 0.9 809 180 3 3.4 896 59 188 510 34 7.2 1.6 225 234 CR Example
    31 B 0.4 796 77 2 1.8 943 15 105 663 29 7.0 1.9 235 244 CR Example
    32 B 0.4 801 83 3 1.2 854 13 105 979 25 7.7 1.2 253 262 CR Example
    33 B 0.4 799 106 3 1.8 933 16 368 866 34 6.7 1.6 216 225 CR Example
    34 B 0.6 793 159 4 3.7 903 12 384 768 25 6.1 1.8 283 290 CR Example
    35 B 0.6 794 76 3 2.2 822 15 199 12 30 8.0 1.2 189 197 CR Example
    36 B 0.9 809 70 2 3.2 863 11 195 34 23 7.4 1.6 249 258 CR Example
    37 B 1.0 795 169 3 4.5 855 18 177 9542 25 7.0 1.3 187 193 CR Example
    38 B 0.3 794 151 4 2.9 935 16 178 9684 40 7.1 1.9 285 294 CR Example
    39 B 0.6 803 150 2 1.9 944 10 209 710 3 7.2 1.1 172 179 CR Example
    40 B 0.8 803 148 3 3.4 965 12 196 557 38 6.0 1.2 213 218 CR Example
    41 B 0.2 791 59 2 3.0 972 13 189 889 88 6.2 1.4 253 258 CR Example
    42 B 0.9 809 188 3 2.6 805 12 184 523 105 6.5 1.2 180 189 CR Comparative Example
    Underlined: indicates value outside scope of present disclosure.
    (*) CR: cold-rolled steel sheet (uncoated), GI: hot-dip galvanized steel sheet (without alloying treatment), GA: galvannealed steel sheet, EG: electrogalvanized steel sheet
    Average heating rate (° C/s) Annealing temp. T1 (°C) Annealing time t1 (s) Number of bends (times) First average cooling rate (°C/s) Second average cooling rate (° C/s) Applied tension (MPa) Tempering temp. T2 (°C) Tempering time t2 (s) Straightening start temp. (°C) Entry side intermesh pressing amount (mm) Delivery intermesh pressing amount (mm) Entry side tension (MPa) Delivery tension (MPa)
    43 B 1.0 794 71 4 3.0 939 19 180 641 39 4.3 2.0 196 202 CR Example
    44 B 0.9 795 71 3 2.7 891 20 191 876 34 2.5 1.2 258 265 CR Comparative Example
    45 B 1.0 808 151 4 2.0 817 20 194 806 25 9.4 1.5 232 239 CR Example
    46 B 0.4 796 160 4 1.3 994 13 196 837 30 9.6 1.0 279 288 CR Example
    47 B 0.7 802 181 5 3.6 958 15 181 728 31 8.0 1.0 299 304 CR Example
    48 B 0.5 800 162 3 3.3 943 18 208 775 37 7.4 1.0 204 211 CR Example
    49 B 0.3 799 101 3 2.9 874 12 184 751 20 9.4 8.4 254 262 CR Example
    50 B 0.4 801 129 4 3.4 840 11 199 580 35 9.6 8.6 257 264 CR Example
    51 B 0.6 799 195 4 1.8 981 14 185 960 20 7.9 1.3 24 31 CR Example
    52 B 0.3 807 115 5 3.4 995 14 180 530 23 6.7 1.1 15 26 CR Comparative Example
    53 B 0.6 795 182 3 4.2 921 18 203 843 32 6.1 1.6 415 423 CR Example
    54 B 0.6 809 83 4 2.2 940 14 171 650 28 7.1 1.9 487 493 CR Example
    55 B 0.9 793 72 2 2.9 950 19 171 526 24 7.4 1.3 26 34 CR Example
    56 B 0.6 796 166 5 3.0 877 11 202 631 40 7.1 1.6 14 27 CR Comparative Example
    57 B 0.9 804 103 4 2.7 838 14 173 796 26 7.5 1.7 487 540 CR Example
    58 B 0.9 800 185 5 3.6 975 11 193 733 40 7.6 1.7 497 545 CR Example
    59 B 0.5 793 123 3 1.8 850 19 170 578 26 6.1 1.9 293 303 GA Example
    60 B 0.7 808 112 3 4.3 867 17 178 583 24 6.2 1.8 276 284 GA Example
    61 C 0.4 806 76 2 2.1 833 12 184 651 34 7.7 1.2 160 167 GA Example
    62 D 0.4 794 171 4 3.0 950 17 193 800 27 7.6 1.7 187 193 GA Example
    63 E 0.3 798 144 5 1.3 838 16 209 792 25 6.5 1.6 242 248 GA Example
    64 F 0.7 806 98 4 4.8 958 10 185 699 39 6.3 1.7 281 286 CR Example
    65 G 0.3 791 84 4 1.6 869 12 195 808 39 8.0 1.2 176 185 CR Comparative Example
    66 H 0.8 797 87 4 1.9 880 18 180 638 36 7.6 1.9 195 204 GA Example
    67 I 0.3 804 111 3 3.6 800 19 188 914 26 6.1 1.8 188 194 GA Comparative Example
    68 J 0.3 806 139 3 1.3 901 12 180 946 24 6.2 1.1 157 164 GI Example
    69 K 0.7 804 96 5 4.0 912 13 191 511 20 7.9 1.1 174 181 GA Comparative Example
    70 L 0.9 803 121 2 1.4 896 13 180 712 34 8.0 1.3 278 286 GA Example
    71 M 0.5 800 153 3 1.9 911 17 184 595 27 7.0 1.9 192 198 GA Comparative Example
    72 N 0.4 797 101 4 1.1 957 14 200 777 39 7.2 1.7 274 280 GA Example
    73 Q 0.4 807 132 3 3.2 940 17 186 650 32 6.3 1.3 261 269 GI Comparative Example
    74 P 0.5 808 92 4 4.1 903 18 188 790 22 6.6 1.1 265 271 GA Example
    75 Q 0.7 800 198 4 1.0 873 15 188 662 24 7.4 1.0 275 282 GA Comparative Example
    76 R 0.7 796 103 3 2.1 888 13 171 769 39 6.0 1.7 223 230 GA Example
    77 S 0.5 793 92 3 2.2 961 16 207 539 35 6.9 1.1 160 165 GA Comparative Example
    78 T 0.5 800 59 2 3.3 918 10 187 658 39 6.8 1.8 249 255 GA Example
    79 U 0.9 795 165 5 2.6 933 12 179 839 29 6.5 1.3 242 252 GI Comparative Example
    80 V 0.8 794 153 4 1.3 979 15 198 797 23 6.4 1.1 176 183 GA Example
    81 W 0.2 797 81 2 2.7 917 10 185 848 29 7.4 2.0 161 170 GA Comparative Example
    82 X 0.3 805 163 3 2.2 853 13 177 717 27 6.0 1.2 152 158 GA Example
    83 Y 1.0 808 103 4 3.0 912 15 178 773 40 6.8 1.5 185 193 GA Comparative Example
    84 Z 0.8 803 63 3 1.1 889 19 178 671 24 7.3 1.8 247 252 CR Example
    Underlined: indicates value outside scope of present disclosure.
    (*) CR: cold-rolled steel sheet (uncoated), GI: hot-dip galvanized steel sheet (without alloying treatment), GA: galvannealed steel sheet, EG: electrogalvanized steel sheet
    Average heating rate (°C/s) Annealing temp. T1 (°C) Annealing time t1 (s) Number of bends (times) First average cooling rate (°C/s) Second average cooling rate (° C/s) Applied tension (MPa) Tempering temp. T2 (°C) Tempering time t2 (s) Straightening start temp. (°C) Entry side intermesh pressing amount (mm) Delivery intermesh pressing amount (mm) Entry side tension (MPa) Delivery tension (MPa)
    85 AA 0.5 810 170 3 1.6 999 11 198 557 25 7.3 1.2 182 187 CR Comparative Example
    86 AB 0.3 797 170 3 4.9 921 14 171 791 29 7.5 1.6 184 190 GA Example
    87 AC 0.6 792 194 5 4.5 948 11 205 758 30 7.1 1.8 280 285 GA Example
    88 AD 0.3 798 132 3 4.4 873 18 187 574 25 6.1 1.9 197 206 GA Example
    89 AE 0.5 791 63 3 3.2 923 20 192 714 37 7.6 2.0 210 217 GA Comparative Example
    90 AF 0.6 803 82 2 3.3 810 19 173 922 22 6.3 1.6 224 233 GA Example
    91 AG 0.5 790 60 4 4.2 977 17 203 526 25 6.8 1.6 277 284 GA Example
    92 AH 0.3 801 56 3 1.4 808 12 202 524 21 7.6 1.4 226 232 GA Comparative Example
    93 AI 0.6 793 126 2 1.8 869 18 179 868 35 6.2 1.1 229 237 CR Example
    94 AJ 0.8 800 179 2 3.0 910 15 172 585 29 6.6 1.2 157 166 CR Example
    95 AK 0.7 796 141 3 5.0 891 13 210 901 39 7.1 1.6 198 206 CR Comparative Example
    96 AL 0.7 791 109 4 3.2 873 16 195 759 33 7.9 1.7 283 290 CR Example
    97 AM 0.2 810 81 4 4.6 941 17 171 672 33 7.6 1.7 244 250 CR Example
    98 AN 0.3 806 194 4 2.9 846 18 174 555 35 7.7 2.0 207 217 CR Comparative Example
    99 AO 0.1 802 188 2 4.2 955 18 208 967 34 7.6 1.3 240 246 CR Example
    100 AP 4.7 804 79 3 4.0 997 10 180 853 29 7.8 2.0 160 169 CR Example
    101 AQ 0.3 757 176 3 1.4 818 15 182 529 21 7.7 1.1 286 294 CR Example
    102 AR 1.0 844 178 4 1.7 883 13 191 551 34 7.6 1.1 217 225 CR Example
    103 AS 0.6 801 15 5 4.6 842 18 171 793 39 6.1 1.7 269 279 CR Example
    104 AT 0.4 799 958 2 2.1 849 20 209 562 35 7.9 1.3 183 190 GA Example
    105 AU 0.6 807 102 1 4.2 849 13 208 892 37 7.1 1.2 219 228 GA Example
    106 AV 0.4 802 160 10 4.2 889 18 194 715 28 6.8 1.4 220 225 CR Example
    107 AW 0.7 800 62 5 0.7 893 16 189 742 22 6.6 1.3 161 166 CR Example
    108 AX 0.2 792 116 3 9.4 856 13 179 641 22 7.2 1.2 283 288 CR Example
    109 AY 0.8 798 103 4 2.5 322 19 180 532 23 6.3 1.2 275 281 EG Example
    110 AZ 0.5 795 73 3 2.1 1891 15 172 677 36 7.1 1.4 184 190 GI Example
    111 BA 0.4 796 180 2 4.2 811 6 196 980 39 6.6 1.2 290 300 EG Example
    112 BB 0.3 802 147 5 2.3 852 46 182 725 37 7.0 1.3 297 305 GI Example
    113 BC 0.8 801 109 5 4.7 824 11 111 517 37 7.6 1.1 160 167 CR Example
    114 BD 0.8 795 51 4 3.5 883 14 368 653 28 7.7 1.1 191 201 CR Example
    115 BE 0.3 795 174 5 3.6 992 13 199 11 29 7.9 1.2 176 185 CR Example
    116 BF 0.4 798 90 5 2.1 968 19 187 9658 29 7.0 1.1 268 274 CR Example
    117 BG 0.3 808 168 3 2.8 976 11 194 908 6 6.3 1.7 265 272 CR Example
    118 BH 1.0 796 122 4 3.0 888 19 196 910 94 7.8 1.0 295 302 CR Example
    119 BI 0.6 797 60 4 1.6 870 19 204 834 34 4.1 1.8 193 200 CR Example
    120 BJ 0.9 791 182 4 1.6 840 13 202 733 23 9.8 1.3 162 169 CR Example
    121 BK 0.7 800 59 3 4.2 840 14 196 929 25 7.1 1.2 24 32 EG Example
    122 BL 0.5 795 94 3 2.4 949 12 207 630 33 7.7 1.3 487 544 GI Example
    123 BM 1.0 806 189 3 2.1 972 19 181 984 34 6.4 1.5 249 255 EG Example
    124 BN 0.7 807 93 2 1.3 852 15 183 857 25 6.8 1.4 256 265 GI Example
    125 BO 0.2 807 58 2 4.5 973 16 186 682 30 7.9 1.1 191 200 GA Example
    Underlined: indicates value outside scope of present disclosure.
    (*) CR: cold-rolled steel sheet (uncoated), GI: hot-dip galvanized steel sheet (without alloying treatment), GA: galvannealed steel sheet, EG: electrogalvanized steel sheet
  • [Table 3]
  • Table 3
    No. Steel sample ID Microstructure* Evaluation result Remarks
    Area fraction Large-angle grain boundary density of tempered M (µm/µm2) KAM(S) /KAM(C) TS EL Toughness after paint baking Crash properties after paint baking
    Tempered M (%) Retained γ (%) F + B (%) TS (MPa) Evaluation EL (%) Evaluation Brittle-ductile transition temp. after aging treatment (°C) Evaluation YR after aging treatment Fracture stress ratio after aging treatment Evaluation
    1 A 88 1 11 1.3 1.05 1341 Good 14 Good -94 Excellent 0.93 0.85 Good Example
    2 B 91 0 9 1.3 1.07 1354 Good 13 Good -94 Excellent 0.94 0.84 Good Example
    3 B 89 1 10 2.5 1.05 1311 Good 12 Good -107 Excellent 0.91 0.82 Good Example
    4 B 89 1 10 1.1 1.07 1356 Good 13 Good -107 Excellent 0.92 0.84 Good Example
    5 B 90 0 10 1.2 1.04 1330 Good 13 Good -49 Good 0.91 0.88 Good Example
    6 B 89 0 11 0.9 1.07 1294 Good 14 Good -15 Poor 0.91 0.95 Poor Comparative Example
    7 B 85 1 14 2.0 1.07 1206 Good 15 Good -105 Excellent 0.91 0.85 Good Example
    8 B 84 1 15 2.0 1.06 1125 Poor 16 Good -102 Excellent 0.90 0.84 Good Comparative Example
    9 B 94 0 6 1.5 1.08 1529 Good 10 Good -94 Excellent 0.91 0.82 Good Example
    10 B 96 1 3 1.8 1.06 1548 Good 8 Poor -97 Excellent 0.92 0.83 Good Comparative Example
    11 B 86 0 14 1.3 1.04 1226 Good 12 Good -109 Excellent 0.94 0.84 Good Example
    12 B 78 1 21 1.7 1.08 984 Poor 18 Good -94 Excellent 0.91 0.83 Good Comparative Example
    13 B 94 0 6 1.2 1.04 1541 Good 10 Good -100 Excellent 0.92 0.82 Good Example
    14 B 99 0 1 1.4 1.08 1541 Good 9 Poor -100 Excellent 0.92 0.81 Good Comparative Example
    15 B 87 1 12 1.1 1.06 1265 Good 13 Good -55 Good 0.92 0.87 Good Example
    16 B 93 0 7 0.7 1.07 1384 Good 11 Good -25 Poor 0.91 0.93 Poor Comparative Example
    17 B 91 1 8 0.9 1.05 1429 Good 12 Good -17 Poor 0.91 0.91 Poor Comparative Example
    18 B 89 0 11 2.8 1.05 1317 Good 13 Good -105 Excellent 0.94 0.84 Good Example
    19 B 86 0 14 1.4 1.03 1223 Good 14 Good -105 Excellent 0.92 0.83 Good Example
    20 B 85 0 15 1.2 1.05 1036 Poor 17 Good -108 Excellent 0.94 0.84 Good Comparative Example
    21 B 94 1 5 2.0 1.06 1542 Good 10 Good -99 Excellent 0.92 0.83 Good Example
    22 B 97 0 3 2.0 1.07 1509 Good 8 Poor -104 Excellent 0.91 0.85 Good Comparative Example
    23 B 89 2 9 1.3 1.06 1388 Good 12 Good -48 Good 0.92 0.84 Good Example
    24 B 85 5 10 1.8 1.03 1350 Good 13 Good -4 Poor 0.90 0.84 Good Comparative Example
    25 B 90 0 10 1.4 1.04 1330 Good 13 Good -104 Excellent 0.91 0.85 Good Example
    26 B 89 1 10 1.4 1.06 1311 Good 12 Good -94 Excellent 0.94 0.84 Good Example
    27 B 87 1 12 1.0 1.03 1289 Good 12 Good -45 Good 0.91 0.90 Good Example
    28 B 87 1 12 0.8 1.05 1248 Good 14 Good -25 Poor 0.92 0.91 Poor Comparative Example
    29 B 89 1 10 1.1 1.05 1315 Good 14 Good -109 Excellent 0.92 0.83 Good Example
    30 B 90 1 9 1.1 1.07 1340 Good 11 Good -100 Excellent 0.92 0.82 Good Example
    31 B 92 1 7 1.3 1.05 1532 Good 11 Good -50 Good 0.93 0.82 Good Example
    32 B 91 1 8 1.8 1.07 1537 Good 10 Good -58 Good 0.92 0.83 Good Example
    33 B 90 1 9 1.7 1.05 1200 Good 13 Good -94 Excellent 0.91 0.81 Good Example
    34 B 91 1 8 1.0 1.08 1207 Good 14 Good -97 Excellent 0.90 0.80 Good Example
    35 B 90 1 9 1.1 1.08 1522 Good 10 Good -49 Good 0.91 0.82 Good Example
    36 B 90 1 9 1.8 1.06 1508 Good 10 Good -48 Good 0.92 0.82 Good Example
    37 B 91 0 9 1.5 1.05 1202 Good 13 Good -91 Excellent 0.92 0.84 Good Example
    38 B 89 0 11 1.1 1.06 1203 Good 13 Good -101 Excellent 0.91 0.81 Good Example
    39 B 91 0 9 1.2 1.05 1374 Good 12 Good -110 Excellent 0.94 0.80 Good Example
    40 B 87 1 12 1.5 1.04 1257 Good 14 Good -93 Excellent 0.90 0.84 Good Example
    41 B 89 1 10 1.4 1.02 1306 Good 13 Good -92 Excellent 0.87 0.81 Good Example
    42 B 90 1 9 1.7 0.97 1376 Good 13 Good -91 Excellent 0.81 0.83 Poor Comparative Example
    Underlined: indicates value outside scope of present disclosure.
    (*) Tempered M: tempered martensite, retained γ: retained austenite, F: ferrite, B: bainitic ferrite
    No. Steel sample ID Microstructure * Evaluation result Remarks
    Area fraction Large-angle grain boundary density of tempered M (µd/µm2) KAM(S) /KAM(C) TS EL Toughness after paint baking Crash properties after paint baking
    Tempered M (%) Retained γ (%) F + B (%) TS (MPa) Evaluation EL (%) Evaluation Brittle-ductile transition temp. after aging treatment (°C) Evaluation YR after aging treatment Fracture stress ratio after aging treatment Evaluation
    43 B 93 0 7 1.6 1.01 1394 Good 11 Good -103 Excellent 0.86 0.81 Good Example
    44 B 90 0 10 1.5 0.92 1359 Good 11 Good -92 Excellent 0.82 0.81 Poor Comparative Example
    45 B 91 0 9 1.4 1.10 1382 Good 12 Good -98 Excellent 0.96 0.84 Good Example
    46 B 88 1 11 1.7 1.14 1274 Good 14 Good -93 Excellent 0.96 0.85 Good Example
    47 B 89 1 10 1.9 1.04 1362 Good 11 Good -90 Excellent 0.87 0.81 Good Example
    48 B 89 1 10 1.7 1.08 1362 Good 12 Good -106 Excellent 0.87 0.82 Good Example
    49 B 88 1 11 1.2 1.15 1311 Good 12 Good -104 Excellent 0.95 0.81 Good Example
    50 B 89 1 10 1.8 1.19 1303 Good 14 Good -101 Excellent 0.96 0.84 Good Example
    51 B 89 0 11 1.1 1.01 1274 Good 13 Good -96 Excellent 0.86 0.84 Good Example
    52 B 89 0 11 1.6 0.99 1280 Good 12 Good -108 Excellent 0.83 0.83 Poor Comparative Example
    53 B 88 1 11 1.6 1.14 1306 Good 14 Good -107 Excellent 0.97 0.85 Good Example
    54 B 91 1 8 1.9 1.19 1412 Good 11 Good -95 Excellent 0.97 0.83 Good Example
    55 B 91 1 8 1.2 1.02 1400 Good 12 Good -105 Excellent 0.86 0.85 Good Example
    56 B 90 1 9 1.7 0.95 1389 Good 12 Good -93 Excellent 0.84 0.85 Poor Comparative Example
    57 B 90 0 10 1.5 1.14 1339 Good 11 Good -109 Excellent 0.96 0.84 Good Example
    58 B 88 1 11 1.4 1.18 1281 Good 13 Good -94 Excellent 0.97 0.83 Good Example
    59 B 89 1 10 1.7 1.06 1303 Good 13 Good -110 Excellent 0.92 0.82 Good Example
    60 B 89 1 10 1.6 1.05 1355 Good 13 Good -96 Excellent 0.93 0.82 Good Example
    61 C 90 0 10 1.4 1.07 1328 Good 11 Good -100 Excellent 0.93 0.83 Good Example
    62 D 88 1 11 1.3 1.05 1268 Good 13 Good -98 Excellent 0.94 0.85 Good Example
    63 E 92 1 7 1.6 1.05 1448 Good 10 Good -110 Excellent 0.91 0.80 Good Example
    64 F 85 1 14 1.0 1.05 1196 Good 14 Good -96 Excellent 0.87 0.80 Good Example
    65 Q 81 0 19 2.0 1.05 1147 Poor 15 Good -91 Excellent 0.84 0.83 Poor Comparative Example
    66 H 95 0 5 1.0 1.05 1526 Good 11 Good -97 Excellent 0.93 0.84 Good Example
    67 I 98 0 2 1.4 1.06 1701 Good 8 Poor -96 Excellent 0.93 0.82 Good Comparative Example
    68 J 92 1 7 1.0 1.04 1227 Good 14 Good -109 Excellent 0.94 0.80 Good Example
    69 K 88 1 11 1.3 1.06 1070 Poor 16 Good -101 Excellent 0.93 0.81 Good Comparative Example
    70 L 91 2 7 2.0 1.06 1568 Good 11 Good -44 Good 0.93 0.81 Good Example
    71 M 85 4 11 1.8 1.06 1433 Good 12 Good -17 Poor 0.92 0.84 Good Comparative Example
    72 N 85 1 14 1.9 1.03 1222 Good 15 Good -99 Excellent 0.90 0.84 Good Example
    73 O 78 1 21 1.6 1.05 1089 Poor 16 Good -104 Excellent 0.93 0.85 Good Comparative Example
    74 P 94 1 5 2.0 1.05 1521 Good 10 Good -102 Excellent 0.92 0.81 Good Example
    75 Q 96 1 3 1.4 1.05 1763 Good 9 Poor -97 Excellent 0.92 0.82 Good Comparative Example
    76 R 93 0 7 1.7 1.07 1379 Good 11 Good -56 Good 0.90 0.82 Good Example
    77 S 92 0 8 1.6 1.04 1429 Good 11 Good 0 Poor 0.91 0.82 Good Comparative Example
    78 T 89 1 10 1.3 1.04 1471 Good 12 Good -45 Good 0.93 0.82 Good Example
    79 U 93 0 7 1.6 1.06 1476 Good 12 Good -7 Poor 0.90 0.83 Good Comparative Example
    80 V 89 0 11 1.0 1.05 1343 Good 13 Good -57 Good 0.91 0.85 Good Example
    81 W 91 1 8 2.0 1.06 1390 Good 13 Good -11 Poor 0.93 0.80 Good Comparative Example
    82 X 88 0 12 1.6 1.05 1281 Good 14 Good -45 Good 0.92 0.84 Good Example
    83 Y 91 0 9 1.5 1.05 1400 Good 12 Good -25 Poor 0.91 0.83 Good Comparative Example
    84 Z 89 1 10 1.1 1.07 1282 Good 14 Good -48 Good 0.93 0.84 Good Example
    Underlined: indicates value outside scope of present disclosure.
    (*) Tempered M: tempered martensite, retained γ: retained austenite, F: ferrite, B: bainitic ferrite
    No. Steel sample ID Microstructure* Evaluation result Remarks
    Area fraction Large-angle grain boundary density of tempered M (µm/µm2) KAM(S) /KAM(C) TS EL Toughness after paint baking Crash properties after paint baking
    Tempered M (%) Retained γ (%) F + B (%) TS (MPa) Evaluation EL (%) Evaluation Brittle-ductile transition temp. after aging treatment (°C) Evaluation YR after aging treatment Fracture stress ratio after aging treatment Evaluation
    85 AA 92 1 7 1.7 1.04 1363 Good 11 Good -4 Poor 0.90 0.81 Good Comparative Example
    86 AB 91 1 8 1.9 1.07 1439 Good 12 Good -102 Excellent 0.93 0.80 Good Example
    87 AC 89 0 11 1.2 1.07 1312 Good 13 Good -103 Excellent 0.93 0.82 Good Example
    88 AD 91 1 8 1.8 1.05 1534 Good 11 Good -49 Good 0.94 0.84 Good Example
    89 AE 88 1 11 1.1 1.07 1702 Good 10 Good -5 Poor 0.91 0.81 Good Comparative Example
    90 AF 91 1 8 1.5 1.06 1384 Good 12 Good -92 Excellent 0.93 0.81 Good Example
    91 AG 91 0 9 1.7 1.04 1522 Good 11 Good -55 Good 0.91 0.81 Good Example
    92 AH 89 0 11 1.7 1.06 1752 Good 11 Good -24 Poor 0.94 0.81 Good Comparative Example
    93 AI 91 1 8 1.3 1.04 1460 Good 11 Good -99 Excellent 0.92 0.84 Good Example
    94 AJ 91 1 8 1.1 1.06 1549 Good 11 Good -46 Good 0.92 0.85 Good Example
    95 AK 91 1 8 1.9 1.06 1787 Good 11 Good -29 Poor 0.92 0.85 Good Comparative Example
    96 AL 90 0 10 1.8 1.07 1350 Good 12 Good -105 Excellent 0.93 0.84 Good Example
    97 AM 89 1 10 1.5 1.08 1522 Good 11 Good -57 Good 0.92 0.82 Good Example
    98 AN 91 0 9 1.8 1.07 1739 Good 10 Good -21 Poor 0.93 0.81 Good Comparative Example
    99 AO 88 1 11 2.6 1.04 1278 Good 12 Good -110 Excellent 0.92 0.81 Good Example
    100 AP 89 0 11 1.1 1.07 1274 Good 14 Good -51 Good 0.93 0.90 Good Example
    101 AQ 86 0 14 1.4 1.07 1192 Good 13 Good -97 Excellent 0.91 0.83 Good Example
    102 AR 94 0 6 1.3 1.03 1522 Good 11 Good -110 Excellent 0.94 0.84 Good Example
    103 AS 85 1 14 1.1 1.06 1192 Good 15 Good -92 Excellent 0.91 0.82 Good Example
    104 AT 93 1 6 1.7 1.05 1509 Good 12 Good -101 Excellent 0.92 0.81 Good Example
    105 AU 93 0 7 1.2 1.05 1467 Good 11 Good -52 Good 0.93 0.86 Good Example
    106 AV 88 0 12 2.9 1.05 1185 Good 16 Good -102 Excellent 0.91 0.81 Good Example
    107 AW 86 0 14 1.2 1.05 1209 Good 14 Good -102 Excellent 0.91 0.83 Good Example
    108 AX 93 1 6 1.9 1.07 1505 Good 11 Good -91 Excellent 0.93 0.85 Good Example
    109 AY 89 2 9 1.5 1.05 1414 Good 12 Good -49 Good 0.91 0.82 Good Example
    110 AZ 89 1 10 1.5 1.06 1275 Good 13 Good -96 Excellent 0.91 0.80 Good Example
    111 BA 90 0 10 1.2 1.04 1325 Good 11 Good -51 Good 0.91 0.88 Good Example
    112 BB 87 1 12 2.0 1.07 1276 Good 12 Good -92 Excellent 0.92 0.80 Good Example
    113 BC 91 0 9 1.8 1.05 1510 Good 11 Good -96 Excellent 0.93 0.84 Good Example
    114 BD 93 0 7 1.9 1.05 1196 Good 10 Good -108 Excellent 0.92 0.82 Good Example
    115 BE 90 1 9 1.2 1.04 1548 Good 10 Good -51 Good 0.90 0.80 Good Example
    116 BF 88 1 11 1.3 1.06 1218 Good 11 Good -106 Excellent 0.91 0.82 Good Example
    117 BG 91 0 9 1.1 1.03 1425 Good 13 Good -91 Excellent 0.94 0.81 Good Example
    118 BH 92 1 7 1.4 1.02 1481 Good 12 Good -106 Excellent 0.86 0.84 Good Example
    119 BI 91 0 9 1.3 1.02 1393 Good 11 Good -101 Excellent 0.87 0.83 Good Example
    120 BJ 88 1 11 1.6 1.12 1336 Good 11 Good -92 Excellent 0.91 0.80 Good Example
    121 BK 91 1 8 1.3 1.02 1454 Good 11 Good -102 Excellent 0.85 0.83 Good Example
    122 BL 91 1 8 1.1 1.14 1436 Good 11 Good -103 Excellent 0.92 0.84 Good Example
    123 BM 92 0 8 1.1 1.07 1482 Good 12 Good -107 Excellent 0.90 0.82 Good Example
    124 BN 89 1 10 1.2 1.07 1408 Good 11 Good -91 Excellent 0.93 0.82 Good Example
    125 BO 91 0 9 1.3 1.07 1495 Good 11 Good -104 Excellent 0.94 0.82 Good Example
    Underlined: indicates value outside scope of present disclosure.
    (*) Tempered M: tempered martensite, retained γ: retained austenite, F: ferrite, B: bainitic ferrite
  • As indicated in Table 3, for the Examples according to the present disclosure, TS, EL, as erll as toughness and crash properties after paint baking, all reached passing criteria. Further, using the steel sheets of the Examples, members obtained by forming and members obtained by joining all had a target shape without crack occurrence, and TS, EL, as well as toughness and crash properties after paint baking, all reached passing criteria.
  • On the other hand, for the Comparative Examples, at least one criterion was failed among TS, EL, and toughness and crash properties after paint baking.

Claims (8)

  1. A steel sheet comprising: a chemical composition containing, in mass%,
    C: 0.030 % or more and 0.500 % or less,
    Si: 0.010 % or more and 2.500 % or less,
    Mn: 0.10 % or more and 5.00 % or less,
    P: 0.100 % or less,
    S: 0.0200 % or less,
    N: 0.0100 % or less,
    O: 0.0100 % or less, and
    Al: 1.000 % or less,
    with the balance being Fe and inevitable impurity; and a steel microstructure wherein
    area fraction of tempered martensite is 83 % or more,
    area fraction of retained austenite is less than 3 %,
    total area fraction of ferrite and bainitic ferrite is 5 % or more and less than 15 %,
    20° or greater grain boundary density in the tempered martensite is 1.0 µm/µm2 or more, and
    the following Expression (1) is satisfied, KAM S / KAM C > 1.00 where
    KAM(S) is an average KAM value at a depth of 100 µm from a surface of the steel sheet, and
    KAM(C) is an average KAM value at a mid-thickness position of the steel sheet.
  2. The steel sheet according to claim 1, wherein the chemical composition further contains, in mass%, at least one selected from the group consisting of
    Ti: 0.200 % or less,
    Nb: 0.200 % or less,
    V: 0.200 % or less,
    Ta: 0.10 % or less,
    W: 0.10 % or less,
    B: 0.0100 % or less,
    Cr: 1.00 % or less,
    Mo: 1.00 % or less,
    Ni: 1.00 % or less,
    Co: 0.010 % or less,
    Cu: 1.00 % or less,
    Sn: 0.200 % or less,
    Sb: 0.200 % or less,
    Ca: 0.0100 % or less,
    Mg: 0.0100 % or less,
    REM: 0.0100 % or less,
    Zr: 0.100 % or less,
    Te: 0.100 % or less,
    Hf: 0.10 % or less, and
    Bi: 0.200 % or less.
  3. The steel sheet according to claim 1, further comprising a coated or plated layer on a surface.
  4. The steel sheet according to claim 2, further comprising a coated or plated layer on a surface.
  5. A member made using the steel sheet according to any one of claims 1 to 4.
  6. A method of producing the steel sheet according to any one of claims 1 to 4, the method comprising:
    a preparation process of preparing a blank sheet having the chemical composition according to claim 1 or 2;
    a heating process of heating the blank sheet under a set of conditions including an average heating rate in a temperature range from 700 °C to 750 °C of 5.0 °C/s or less, and
    heating to an annealing temperature T1;
    an annealing process of annealing the blank sheet under a set of conditions including the annealing temperature T1 being 750 °C or more and 850 °C or less, and
    an annealing time t1 of 10 s or longer and 1000 s or shorter;
    a bending process of applying bending once or more to the blank sheet using a roller that has a radius of 800 mm or less in a temperature range from the annealing temperature T1 to 700 °C;
    a first cooling process of cooling the blank sheet under a set of conditions including an average cooling rate in a temperature range from 700 °C to 550 °C of 0.5 °C/s or more and less than 10.0 °C/s,
    to a first cooling end temperature;
    a second cooling process of cooling the blank sheet under a set of conditions including an average cooling rate in a temperature range from 300 °C to 100 °C of 300 °C/s or more, and
    applying tension to the blank sheet in the temperature range from 300 °C to 100 °C of 5 MPa or more,
    to a second cooling end temperature;
    a tempering process of tempering the blank sheet under a set of conditions including a tempering temperature T2 of 100 °C or more and 400 °C or less, and
    a tempering time t2 of 10 s or longer and 10,000 s or shorter; and
    a straightening process of applying straightening to the blank sheet by leveling under a set of conditions including a straightening start temperature of 100 °C or less,
    an entry side intermesh pressing amount of 4.0 mm or more and 10.0 mm or less,
    a delivery intermesh pressing amount of 1.0 mm or more and 10.0 mm or less,
    an entry side tension of 20 MPa or more and 500 MPa or less, and
    a delivery tension of 25 MPa or more and 550 MPa or less.
  7. The method of producing a steel sheet according to claim 6, further comprising a coating or plating process of applying a coating or plating treatment to the blank sheet between the first cooling process and the second cooling process, or between the tempering process and the straightening process.
  8. A method of producing a member, wherein the steel sheet according to any one of claims 1 to 4 is subjected to at least one of a forming process or a joining process to produce the member.
EP23928769.1A 2023-03-23 2023-11-21 Steel sheet and member, and method for producing said steel sheet and method for producing said member Pending EP4656755A1 (en)

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PCT/JP2023/041851 WO2024195201A1 (en) 2023-03-23 2023-11-21 Steel sheet and member, and method for producing said steel sheet and method for producing said member

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JP6497443B2 (en) 2015-08-31 2019-04-10 新日鐵住金株式会社 steel sheet
JP6747612B1 (en) 2018-10-10 2020-08-26 Jfeスチール株式会社 High-strength steel sheet and method for manufacturing the same
JP7001197B2 (en) 2020-01-31 2022-01-19 Jfeスチール株式会社 Steel sheets, members and their manufacturing methods

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WO2017212885A1 (en) * 2016-06-06 2017-12-14 株式会社神戸製鋼所 High strength cold-rolled steel sheet with excellent moldability and manufacturing method therefor
EP3992314A4 (en) * 2019-06-28 2023-07-19 Nippon Steel Corporation Steel sheet
CN114929918B (en) * 2020-01-30 2023-12-26 日本制铁株式会社 Hot-rolled steel plate and manufacturing method
JP7606111B2 (en) * 2021-01-07 2024-12-25 日本製鉄株式会社 Steel plate and its manufacturing method
US12428700B2 (en) * 2021-06-11 2025-09-30 Jfe-Steel Corporation High strength steel sheet and method for manufacturing the same
MX2023014591A (en) * 2021-06-11 2023-12-15 Jfe Steel Corp High-strength steel sheet and manufacturing method therefor.

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Publication number Priority date Publication date Assignee Title
JP6497443B2 (en) 2015-08-31 2019-04-10 新日鐵住金株式会社 steel sheet
JP6747612B1 (en) 2018-10-10 2020-08-26 Jfeスチール株式会社 High-strength steel sheet and method for manufacturing the same
JP7001197B2 (en) 2020-01-31 2022-01-19 Jfeスチール株式会社 Steel sheets, members and their manufacturing methods

Non-Patent Citations (1)

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Title
See also references of WO2024195201A1

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KR20250156161A (en) 2025-10-31
CN120677260A (en) 2025-09-19
JP7597272B1 (en) 2024-12-10
WO2024195201A1 (en) 2024-09-26
MX2025009602A (en) 2025-09-02

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