Classifications

• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
  • C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
  • C21D1/02—Hardening articles or materials formed by forging or rolling, with no further heating beyond that required for the formation
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
  • C21D1/84—Controlled slow cooling
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D6/00—Heat treatment of ferrous alloys
  • C21D6/001—Heat treatment of ferrous alloys containing Ni
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D6/00—Heat treatment of ferrous alloys
  • C21D6/002—Heat treatment of ferrous alloys containing Cr
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D6/00—Heat treatment of ferrous alloys
  • C21D6/005—Heat treatment of ferrous alloys containing Mn
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D6/00—Heat treatment of ferrous alloys
  • C21D6/008—Heat treatment of ferrous alloys containing Si
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/0205—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips of ferrous alloys
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/0221—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
  • C21D8/0226—Hot rolling
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/0247—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/0247—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
  • C21D8/0263—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment following hot rolling
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/001—Ferrous alloys, e.g. steel alloys containing N
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/005—Ferrous alloys, e.g. steel alloys containing rare earths, i.e. Sc, Y, Lanthanides
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/08—Ferrous alloys, e.g. steel alloys containing nickel
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/16—Ferrous alloys, e.g. steel alloys containing copper
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
  • C22C38/28—Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
  • C22C38/32—Ferrous alloys, e.g. steel alloys containing chromium with boron
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
  • C22C38/38—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
  • C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
  • C22C38/58—Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/60—Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D2211/00—Microstructure comprising significant phases
  • C21D2211/001—Austenite
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D2211/00—Microstructure comprising significant phases
  • C21D2211/002—Bainite
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D2211/00—Microstructure comprising significant phases
  • C21D2211/008—Martensite

Definitions

• the present invention relates to a high-strength steel sheet and a method for manufacturing the high-strength steel sheet.
• aspects of the present invention relate to a high-strength steel sheet that has a tensile strength of 980 MPa or more, a uniform elongation of 6% or more, and high bendability, and that is suitable as a material for a frame, a suspension component, or the like of a truck or a passenger car, and a method for manufacturing the high-strength steel sheet.
• Automotive parts particularly chassis parts, such as suspension components, need to have complex shapes to ensure rigidity.
• materials for automotive parts require high press formability or ductility.
• steel sheets with increased tensile strength tend to have a crack during bending.
• a crack in a bent portion may become a fatigue crack initiation point and may result in parts with lower durability than assumed in the design.
• materials for automotive parts and the like require high bendability.
• Patent Literature 1 to Patent Literature 6 has problems as described below.
• Patent Literature 1 and Patent Literature 2 cannot achieve a tensile strength of 980 MPa or more.
• elongation is used as a measure of workability.
• necking occurs before breakage. Necking locally reduces the thickness of the sheet and results in a defective product during press forming. Thus, high total elongation is not sufficient for high press formability.
• Patent Literature 1 and Patent Literature 2 do not describe bendability.
• aspects of the present invention have been made in view of such situations and aim to provide a high-strength steel sheet with high tensile strength, press formability, and bendability, and a method for manufacturing the high-strength steel sheet.
• the present inventors made hypothetical stress-strain curves of steel sheets with a tensile strength of 980 MPa or more and with various yield stresses and uniform elongations, and performed a press forming simulation of a suspension component using the stress-strain curves. The characteristics of a steel sheet required for high press formability were examined on the basis of the results of the simulation.
• a steel sheet with a tensile strength of 980 MPa or more can have the minimum thickness reduction during press forming and is less likely to have press forming defects.
• the present inventors have also studied an optimum steel sheet microstructure to achieve a tensile strength of 980 MPa or more and a uniform elongation of 6% or more. As a result, it was found that a microstructure that contains upper bainite as a main phase and contains an appropriate amount of hard second phase containing fresh martensite and/or retained austenite can achieve both a high strength of 980 MPa or more and a uniform elongation of 6% or more.
• upper bainite refers to an aggregate of lath ferrite with an orientation difference of less than 15 degrees and refers to a microstructure with Fe-based carbide and/or retained austenite between lath ferrites (including a microstructure without Fe-based carbide and/or retained austenite between lath ferrites).
• lath ferrite has a lath shape and has a relatively high dislocation density inside, so that they can be distinguished with a scanning electron microscope (SEM) or a transmission electron microscope (TEM).
• the fresh martensite refers to martensite without Fe-based carbide.
• Fresh martensite and retained austenite have a similar contrast in SEM but can be distinguished by an electron backscatter diffraction patterns (EBSD) method.
• EBSD electron backscatter diffraction patterns
• the present inventors examined the bendability of a high-strength steel sheet with a tensile strength of 980 MPa or more and a uniform elongation of 6% or more. More specifically, steel sheets with a tensile strength of 980 MPa or more and a uniform elongation of 6% or more manufactured by different manufacturing methods were subjected to a 90-degree V bending test, and a fracture surface of a flex crack and the microstructure near the crack were observed. On the outside of the bend, a crack fracture surface was a ductile fracture surface, and many voids were observed in the microstructure near the crack, indicating that cracking outside the bend was ductile fracture.
• a crack fracture surface was a brittle fracture surface, and no voids were observed in the microstructure near the crack.
• cracking inside the bend was brittle fracture due to strong compression.
• the improvement of ductility can reduce cracking outside the bend, and the improvement of compression embrittlement resistance characteristics can reduce cracking inside the bend.
• the microstructure should be controlled in a surface layer region where a flex crack can be formed and in the vicinity thereof.
• a high-strength steel sheet which comprises:
• RC 1(° C.) 900+100 ⁇ C+ 100 ⁇ N+ 10 ⁇ Mn+ 700 ⁇ Ti+ 5000 ⁇ B+ 10 ⁇ Cr+ 50 ⁇ Mo+ 2000 ⁇ Nb+ 150 ⁇ V (1)
• Trs (° C.) 500 ⁇ 450 ⁇ C— 35 ⁇ Mn ⁇ 15 ⁇ Cr— 10 ⁇ Ni ⁇ 20 ⁇ Mo (3)
• aspects of the present invention can provide a high-strength steel sheet with a tensile strength of 980 MPa or more, high press formability, and high bendability.
• a high-strength steel sheet according to aspects of the present invention has high press formability in spite of high tensile strength and can be press-formed without a forming defect, such as necking or cracking.
• the application of a high-strength steel sheet according to aspects of the present invention to a member of a truck or a passenger car can reduce the amount of steel material used while ensuring safety, and reduce the weight of the automobile body, thus contributing to reducing the effects on the environment.
• high press formability refers to a uniform elongation of 6% or more.
• high bendability means that the ratio R/t of the critical bending radius R at which no crack with a depth of 50 ⁇ m or more is formed both outside and inside the bend in a 90-degree V bending test to the thickness t of a steel sheet is 1.5 or less.
• C is an element with the effect of improving the strength of steel.
• C improves hardenability, thereby promotes the formation of bainite, and contributes to increase the strength.
• C increases the strength of martensite and also contributes to increase the strength.
• the C content should be 0.05% or more.
• the C content is 0.05% or more, preferably 0.06% or more.
• a C content of more than 0.20% results in martensite with excessively increased strength, a larger difference in strength between upper bainite serving as a main phase and fresh martensite and/or retained austenite, and consequently lower uniform elongation.
• the C content is 0.20% or less, preferably 0.18% or less.
• Si has the effect of reducing the formation of Fe-based carbide and reduces the precipitation of cementite during upper bainite transformation. This distributes C to non-transformed austenite, and cooling after coiling in a hot-rolling process transforms the non-transformed austenite into fresh martensite and/or retained austenite, thereby forming the desired fresh martensite and/or retained austenite.
• These effects require a Si content of 0.5% or more, preferably 0.6% or more.
• a Si content of more than 1.2% may result in the formation of fresh martensite and/or retained austenite in an amount larger than the desired area ratio, consequently an undesired area ratio of upper bainite, and lower bendability.
• the Si content is 1.2% or less, preferably 1.1% or less.
• Mn stabilizes austenite and contributes to the formation of fresh martensite and/or retained austenite. Such effects require a Mn content of 1.5% or more. Thus, the Mn content is 1.5% or more, preferably 1.7% or more. On the other hand, a Mn content of more than 4.0% results in excessive formation of fresh martensite and/or retained austenite, consequently an undesired area ratio of upper bainite, and lower bendability. Thus, the Mn content is 4.0% or less, preferably 3.8% or less.
• P is an element that contributes to an increase in the strength of steel through solid solution.
• P is also an element that segregates at an austenite grain boundary during hot rolling and thereby causes slab cracking during the hot rolling. P also segregates at a grain boundary and reduces the uniform elongation.
• the P content is preferably minimized and may be 0.10% or less.
• the P content is 0.10% or less.
• the lower limit is not particularly limited, the P content is preferably 0.0002% or more because a P content of less than 0.0002% causes a decrease in production efficiency.
• the S content is preferably minimized and may be 0.03% or less.
• the S content is 0.03% or less.
• the S content is preferably 0.0002% or more because a S content of less than 0.0002% causes a decrease in production efficiency.
• Al is an element that acts as a deoxidizing agent and is effective in improving the cleanliness of steel. This effect is insufficient at an Al content of less than 0.001%.
• the Al content is 0.001% or more, preferably 0.005% or more, more preferably 0.010% or more.
• Al is effective in reducing the formation of Fe-based carbide and reduces the precipitation of cementite during upper bainite transformation. This contributes to the formation of fresh martensite and/or retained austenite during cooling after coiling.
• an excessively high Al content results in an increased number of oxide inclusions and lower uniform elongation.
• the Al content is 2.0% or less, preferably 1.0% or less, more preferably 0.1% or less.
• N binds to a nitride-forming element, thereby precipitates as a nitride, and generally contributes to grain refinement.
• N binds to Ti at high temperatures and forms a coarse nitride.
• a N content of more than 0.01% results in lower uniform elongation.
• the N content is 0.01% or less.
• the N content is preferably 0.0002% or more because a N content of less than 0.0002% causes a decrease in production efficiency.
• the O content should be reduced. In particular, this tendency is remarkable at an O content of more than 0.01%.
• the O content is 0.01% or less, preferably 0.005%, more preferably 0.003%.
• the O content is preferably 0.00005% or more because the production efficiency may be significantly lowered at an O content of less than 0.00005%.
• B is an element that segregates in a prior-austenite grain boundary, reduces the formation of ferrite, thereby promotes the formation of upper bainite, and contributes to improving the strength of a steel sheet.
• These effects require a B content of 0.0005% or more.
• the B content is 0.0005% or more, preferably 0.0006% or more, more preferably 0.0007% or more.
• these effects are saturated at a B content of more than 0.010%.
• the B content is 0.010% or less, preferably 0.009% or less, more preferably 0.008% or less.
• the remainder is composed of Fe and incidental impurities.
• the incidental impurities include Zr, Co, Sn, Zn, and W.
• the chemical composition contains at least one of Zr, Co, Sn, Zn, and W as incidental impurities, the total amount of the element(s) is preferably 0.5% or less.
• the chemical composition of a high-strength steel sheet according to aspects of the present invention may optionally contain at least one of the following elements.
• Cr is a carbide-forming element and has the effect of reducing driving force for bainite transformation by segregating at an interface between upper bainite and non-transformed austenite during upper bainite transformation before coiling, thereby stopping the upper bainite transformation.
• Non-transformed austenite remained due to the stopped upper bainite transformation becomes fresh martensite and/or retained austenite by cooling after coiling.
• Cr if added, also contributes to the formation of a desired area ratio of fresh martensite and/or retained austenite. This effect is preferably produced at a Cr content of 0.1% or more.
• a Cr content of more than 1.0% results in excessive formation of fresh martensite and/or retained austenite, consequently an undesired area ratio of upper bainite, and lower bendability.
• the Cr content is 1.0% or less, preferably 0.9% or less, more preferably 0.8% or less.
• Mo promotes the formation of bainite through the improvement of hardenability and contributes to improving the strength of a steel sheet.
• Mo is a carbide-forming element, segregates at an interface between upper bainite and non-transformed austenite during upper bainite transformation before coiling, thereby reduces transformation driving force for bainite, and contributes to the formation of fresh martensite and/or retained austenite after coiling and cooling.
• a Mo content of more than 1.0% results in excessive formation of fresh martensite and/or retained austenite, consequently an undesired area ratio of upper bainite, and lower uniform elongation. This effect is preferably produced at a Mo content of 0.1% or more.
• the Mo content is 1.0% or less, preferably 0.9% or less, more preferably 0.8% or less.
• the chemical composition of a high-strength steel sheet according to aspects of the present invention may optionally contain at least one of the following elements.
• Cu is an element that contributes to an increase in the strength of steel through solid solution.
• Cu promotes the formation of bainite through the improvement of hardenability and contributes to improving the strength. This effect is preferably produced at a Cu content of 0.01% or more.
• a Cu content of more than 2.0% results in a high-strength steel sheet with lower surface quality and bendability.
• the Cu content is 2.0% or less, preferably 1.9% or less, more preferably 1.8% or less.
• Ni is an element that contributes to an increase in the strength of steel through solid solution. Ni promotes the formation of bainite through the improvement of hardenability and contributes to improving the strength. This effect is preferably produced at a Ni content of 0.01% or more. However, a Ni content of more than 2.0% results in an excessive increase of fresh martensite and/or retained austenite, consequently an undesired area ratio of upper bainite, and a high-strength steel sheet with lower ductility. Thus, when Ni is added, the Ni content is 2.0% or less, preferably 1.9% or less, more preferably 1.8% or less.
• Ti is an element with the effect of improving the strength of a steel sheet by precipitation strengthening or solid-solution strengthening. Ti forms a nitride in a high-temperature region of austenite. This reduces the precipitation of BN and results in B in a solid solution state. Thus, Ti, if added, also contributes to ensuring hardenability necessary for the formation of upper bainite and improves the strength. This effect is preferably produced at a Ti content of 0.01% or more. However, a Ti content of more than 0.3% results in a large amount of Ti nitride and lower uniform elongation. Thus, when Ti is added, the Ti content is 0.3% or less, preferably 0.28% or less, more preferably 0.25% or less.
• Nb is an element with the effect of improving the strength of a steel sheet by precipitation strengthening or solid-solution strengthening. Like Ti, Nb increases the recrystallization temperature of austenite during hot rolling, thereby enables rolling in an austenite non-recrystallization temperature range, and contributes to decreasing the grain size of upper bainite and increasing the area ratio of fresh martensite and/or retained austenite. Like Cr, Nb is a carbide-forming element and is an element that segregates at an interface between upper bainite and non-transformed austenite during upper bainite transformation before coiling and thereby has the effect of reducing transformation driving force for bainite and stopping the upper bainite transformation while leaving the non-transformed austenite.
• the non-transformed austenite becomes fresh martensite and/or retained austenite by cooling thereafter.
• Nb if added, also contributes to the formation of a desired area ratio of fresh martensite and/or retained austenite. This effect is preferably produced at a Nb content of 0.01% or more.
• a Nb content of more than 0.3% results in an excessive increase of fresh martensite and/or retained austenite, consequently an undesired area ratio of upper bainite, and lower uniform elongation.
• the Nb content is 0.3% or less, preferably 0.28% or less, more preferably 0.25% or less.
• V is an element with the effect of improving the strength of a steel sheet by precipitation strengthening and solid-solution strengthening. Like Ti, V increases the recrystallization temperature of austenite during hot rolling, thereby enables rolling in an austenite non-recrystallization temperature range, and contributes to decreasing the grain size of upper bainite. Like Cr, V is a carbide-forming element and is an element that segregates at an interface between upper bainite and non-transformed austenite during upper bainite transformation before coiling and thereby has the effect of reducing transformation driving force for bainite and stopping the upper bainite transformation while leaving the non-transformed austenite. The non-transformed austenite becomes fresh martensite and/or retained austenite by cooling thereafter.
• V if added, also contributes to the formation of a desired area ratio of fresh martensite and/or retained austenite.
• This effect is preferably produced at a V content of 0.01% or more.
• a V content of more than 0.3% results in an excessive increase of fresh martensite and/or retained austenite, consequently an undesired area ratio of upper bainite, and lower uniform elongation.
• the V content is 0.3% or less, preferably 0.28% or less, more preferably 0.25% or less.
• composition of a high-strength steel sheet according to aspects of the present invention may further optionally contain the following elements.
• Sb is an element with the effect of reducing nitriding of the surface of a steel material (slab) when the steel material is heated.
• the addition of Sb can reduce the precipitation of BN in a surface layer portion of a steel material.
• remaining solid solution B contributes to ensuring hardenability necessary for the formation of bainite and thereby improving the strength of a steel sheet.
• the Sb content is 0.005% or more, preferably 0.006% or more, more preferably 0.007% or more, to produce the effects.
• an Sb content of more than 0.020% results in steel with lower toughness and may cause slab cracking and hot-rolling cracking.
• the Sb content is 0.020% or less, preferably 0.019% or less, more preferably 0.018% or less.
• the chemical composition of a high-strength steel sheet according to aspects of the present invention may optionally contain at least one of the following elements.
• the following elements contribute to further improvement of press formability or other characteristics.
• Ca controls the shape of an oxide or sulfide inclusion and contributes to reducing cracking of a sheared end face of a steel sheet and further improving the bendability of a steel sheet. This effect is preferably produced at a Ca content of 0.001% or more. However, a Ca content of more than 0.01% may result in an increase of a Ca-based inclusion and steel with lower cleanliness and rather result in sheared end face cracking or bending cracking. Thus, when Ca is added, the Ca content is 0.01% or less.
• Mg controls the shape of an oxide or sulfide inclusion and contributes to reducing cracking of a sheared end face of a steel sheet and further improving the bendability of a steel sheet. This effect is preferably produced at a Mg content of 0.001% or more. However, a Mg content of more than 0.01% may result in steel with lower cleanliness and rather result in sheared end face cracking or bending cracking. Thus, when Mg is added, the Mg content is 0.01% or less.
• a rare-earth metal controls the shape of an oxide or sulfide inclusion and contributes to reducing cracking of a sheared end face of a steel sheet and further improving the bendability of a steel sheet.
• This effect is preferably produced at a REM content of 0.001% or more.
• a REM content of more than 0.01% may result in steel with lower cleanliness and rather result in sheared end face cracking or bending cracking.
• the REM content is 0.01% or less.
• a high-strength steel sheet has a microstructure containing 80% by area or more of upper bainite and 2% by area or more of fresh martensite and/or retained austenite in total in a surface layer region extending from a surface of the steel sheet to a position of one-tenth of the thickness of the steel sheet and 70% by area or more of upper bainite and 3% by area or more of fresh martensite and/or retained austenite in total in an inner region extending from a position of one-tenth to a position of three-tenths of the thickness of the steel sheet.
• the surface layer region extending from the surface of the steel sheet to the position of one-tenth of the thickness of the steel sheet has an average grain size of 6 ⁇ m or less.
• a difference (HV2 ⁇ HV1) between a hardness (HV1) of the surface layer region extending from the surface of the steel sheet to the position of one-tenth of the thickness of the steel sheet and a hardness (HV2) of the inner region extending from the position of one-tenth to the position of three-tenths of the thickness of the steel sheet is 5% or more and 15% or less of [0.3 ⁇ tensile strength (MPa)].
• Upper bainite 80% or more and fresh martensite and/or retained austenite: 2% by area or more in total in surface layer region extending from surface of steel sheet to position of one-tenth of thickness of steel sheet
• hard fresh martensite and/or retained austenite can be finely dispersed in soft upper bainite to improve ductility and reduce cracking outside the bend.
• the area fraction of upper bainite is 80% or more, and the area ratio of fresh martensite and/or retained austenite is 2% or more.
• the area ratio of upper bainite is 85% or more, and the area ratio of fresh martensite and/or retained austenite is 3% or more.
• the bendability may be lowered when the total area ratio of fresh martensite and/or retained austenite is 20% or more.
• the total area ratio of fresh martensite and/or retained austenite is therefore preferably 20% or less, more preferably 18% or less, still more preferably 15% or less.
• an inner region extending from a position of one-tenth to a position of three-tenths of the thickness of a steel sheet contains upper bainite as a main phase.
• the upper bainite has an area ratio of less than 70%, a tensile strength of 980 MPa or more and a uniform elongation of 6% or more cannot be achieved.
• the upper bainite has an area ratio of 70% or more, preferably 80% or more.
• an inner region extending from a position of one-tenth to a position of three-tenths of the thickness of a steel sheet contains fresh martensite and/or retained austenite.
• Fresh martensite has the effect of promoting work hardening, delaying the onset of plastic instability, and thereby improving the uniform elongation.
• Retained austenite can improve the uniform elongation by the transformation induced plasticity (TRIP) effect.
• TRIP transformation induced plasticity
• the total area ratio of fresh martensite and/or retained austenite is 3% or more, preferably 4% or more.
• the area ratio of upper bainite is preferably 60% or more from the perspective of ductility, although the effect on bendability is small. 40% or less of fresh martensite/tempered martensite/retained austenite and the like may be contained due to Mn segregation at half the thickness of a steel sheet.
• Average grain size in surface layer region extending from surface of steel sheet to position of one-tenth of thickness of steel sheet 6 ⁇ m or less
• the average grain size in a surface layer region is 6 ⁇ m or less, preferably 5 ⁇ m or less.
• compression embrittlement resistance is improved as the average grain size decreases, an excessively small average grain size may result in higher strength and lower elongation and cracking in outer bending.
• the average grain size in the surface layer region is preferably 2 ⁇ m or more.
• a tensile strength of 980 MPa or more, a uniform elongation of 6% or more, and high bendability can be achieved only by combining the uniform elongation improving effect of fresh martensite and/or retained austenite with the flex cracking suppressive effect by controlling a surface layer microstructure.
• HV2 ⁇ HV1 hardness (HV1) of surface layer region extending from surface of steel sheet to a position of one-tenth of thickness of steel sheet and hardness (HV2) of inner region extending from a position of one-tenth to a position of three-tenths of thickness of steel sheet is 5% or more and 15% or less of [0.3 ⁇ tensile strength (MPa)]
• a soft surface layer reduces cracking outside the bend, and a hard inner portion adjacent to the surface layer reduces the growth of a flex crack in the thickness direction of the steel sheet.
• the difference (HV2 ⁇ HV1) between the hardness (HV1) of the surface layer region and the hardness (HV2) of the inner region is 5% or more, preferably 6% or more, more preferably 7% or more, with respect to 0.3 ⁇ tensile strength (MPa).
• the difference between the hardness of the surface layer region and the hardness of the inner region is 15% or less, preferably 14% or less, more preferably 13% or less, with respect to 0.3 ⁇ tensile strength (MPa).
• MPa tensile strength
• the microstructure may further contain a microstructure other than upper bainite, fresh martensite, and retained austenite (hereinafter referred to as “another microstructure”). From the perspective of enhancing the effect of microstructure control, another microstructure preferably has a total area ratio of 3% or less. In other words, the upper bainite, fresh martensite, and retained austenite in the microstructure preferably have a total area ratio of 97% or more. Examples of the other microstructure include cementite, polygonal ferrite, pearlite, tempered martensite, and lower bainite.
• a high-strength steel sheet according to aspects of the present invention has a tensile strength of 980 MPa or more, a uniform elongation of 6% or more, and an R/t (the ratio of the critical bending radius R at which no crack with a depth of 50 ⁇ m or more is formed both outside and inside the bend to the thickness t of the steel sheet) of 1.5 or less.
• a high-strength steel sheet according to aspects of the present invention has high press formability in spite of its high tensile strength, can be press-formed without a forming defect, such as necking or cracking, and can ensure the durability of a component without forming a large crack outside and inside a bent portion.
• a high-strength steel sheet according to aspects of the present invention applied to a member of a truck or a passenger car can ensure safety.
• microstructure, hardness, and mechanical properties in accordance with aspects of the present invention can be determined by measurement methods described below in Examples.
• the temperature in the following description represents the surface temperature of an object (a steel material or a steel sheet).
• a high-strength steel sheet according to aspects of the present invention can be manufactured by sequentially subjecting a steel material to the following treatments (1) to (5). Each of the steps is described below.
• the steel material may be any material with the chemical composition described above.
• the chemical composition of the final high-strength steel sheet is the same as the chemical composition of the steel material used.
• the steel material can be a steel slab, for example.
• the steel material may be manufactured by any method.
• a molten steel with the chemical composition described above can be obtained by steelmaking by a known method using a converter or the like, and a steel material can be manufactured by a casting method, such as continuous casting. It is also possible to use a method other than the continuous casting method, such as an ingot casting and blooming method. Scrap may also be used as a raw material.
• the steel material manufactured by the continuous casting method or the like may be directly subjected to the next heating step or may be cooled and subjected as a hot piece or a cold piece to the heating step.
• the steel material is heated to a heating temperature of 1150° C. or more.
• carbonitride-forming elements such as Ti
• coarse carbonitrides in steel materials.
• the presence of the coarse and nonuniform precipitates causes degradation of various characteristics generally required for high-strength steel sheets for truck and passenger car components (for example, sheared edge cracking resistance, bendability, burring formability, and the like).
• the steel material should be heated before hot rolling to dissolve coarse precipitates. More specifically, the heating temperature of the steel material should be 1150° C. or more to sufficiently dissolve coarse precipitates.
• an excessively high heating temperature of the steel material results in the occurrence of a slab defect and a decrease in yield due to scaling off.
• the heating temperature of the steel material is preferably 1350° C. or less.
• the lower limit of the heating temperature of the steel material is more preferably 1180° C. or more, still more preferably 1200° C. or more.
• the upper limit of the heating temperature of the steel material is more preferably 1300° C. or less, still more preferably 1280° C. or less.
• the temperature of the steel material is preferably increased to the heating temperature and is then maintained at the heating temperature.
• the holding time at the heating temperature is preferably, but not limited to, 1800 seconds or more from the perspective of improving the temperature uniformity of the steel material.
• a holding time of more than 10,000 seconds results in an increased amount of scales. This often causes scale biting or the like in the subsequent hot rolling and decreases the yield due to defective surface flaws.
• the holding time is preferably 10,000 seconds or less, more preferably 8000 seconds or less.
• the heated steel material is then hot-rolled to form a hot-rolled steel sheet.
• the hot rolling may include rough rolling and finish rolling.
• the rough rolling may be performed under any conditions.
• descaling is preferably performed to remove surface scales before the finish rolling. In the finish rolling, descaling may be performed between stands.
• the total rolling reduction at a temperature of RC1 or less is 25% or more and 80% or less, and the finishing temperature is (RC2 ⁇ 50° C.) or more and (RC2+120° C.) or less.
• RC1 denotes the austenite 50% recrystallization temperature estimated from the chemical composition
• RC2 denotes the austenite recrystallization lower limit temperature estimated from the chemical composition.
• the total rolling reduction at RC1 or less is less than 25%, the average grain size increases, and high bendability cannot be achieved.
• the total rolling reduction at a temperature of RC1 or less is more than 80%, austenite has a high dislocation density, a bainite microstructure transformed from the austenite with a high dislocation density has low ductility, and the uniform elongation of 6% or more cannot be achieved.
• the total rolling reduction at a temperature of RC1 or less is 25% or more and 80% or less.
• the hot rolling is performed under the condition of finishing temperature: (RC2 ⁇ 50° C.) or more and (RC2+120° C.) or less.
• finishing temperature (RC2 ⁇ 50° C.) or more and (RC2+120° C.) or less.
• a finishing temperature below (RC2 ⁇ 50° C.) bainite transformation occurs from austenite with a high dislocation density.
• Upper bainite transformed from austenite with a high dislocation density has a high dislocation density and low ductility, resulting in a decrease in the uniform elongation.
• the uniform elongation also decreases when the finish rolling temperature is low and the rolling is performed at a two-phase temperature of ferrite+austenite.
• the finishing temperature is (RC2 ⁇ 50° C.) or more.
• RC1 and RC2 are defined by the following formulae (1) and (2):
• RC 1(° C.) 900+100 ⁇ C+ 100 ⁇ N+ 10 ⁇ Mn+ 700 ⁇ Ti+ 5000 ⁇ B+ 10 ⁇ Cr+ 50 ⁇ Mo+ 2000 ⁇ Nb+ 150 ⁇ V (1)
• the hot-rolled steel sheet thus manufactured is cooled (first cooling).
• the time from completion of the hot rolling (completion of the finish rolling) to the start of the cooling (cooling start time) is 2.0 seconds or less.
• a cooling start time of more than 2.0 seconds results in the growth of austenite grains, thus failing to achieve a tensile strength of 980 MPa or more.
• the cooling start time is preferably 1.5 seconds or less.
• the average cooling rate at a position of three-tenths of the thickness of the steel sheet is 15° C./s or more.
• the surface layer is cooled more rapidly than the inside to form a microstructure that differs between the surface layer and the inside.
• the rapid cooling of the surface layer advances the bainite transformation start in the surface layer and forms a smaller amount of martensite and retained austenite due to carbon concentrating in the surface layer than in the inside.
• the average cooling rate of the cooling is less than 15° C./s, the surface layer is not sufficiently rapidly cooled, and the surface layer microstructure containing 80% by area or more of upper bainite and 2% by area or more of fresh martensite and/or retained austenite in total cannot be formed.
• the average cooling rate is 15° C./s or more, preferably 20° C./s or more, more preferably 50° C./s or more.
• the average cooling rate may have any upper limit, an excessively high average cooling rate makes it difficult to control the cooling stop temperature.
• the average cooling rate is preferably 200° C./s or less.
• the average cooling rate is specified on the basis of the average cooling rate at the surface of the steel sheet.
• the average cooling rate of the surface layer ⁇ the average cooling rate at a position of three-tenths of the thickness of the steel sheet is 10° C./s or more
• the formation of martensite or retained austenite due to carbon concentrating in the surface layer is less than that at the position of three-tenths of the thickness of the steel sheet. Consequently, a soft surface layer microstructure can be formed.
• the cooling rate is lower than that in the surface layer, and the progress of the bainite transformation is slower than that in the surface layer, so that the formation of martensite or retained austenite due to carbon concentrating is more than in the surface layer, and an internal microstructure with high hardness can be formed.
• the average cooling rate of the surface layer ⁇ the average cooling rate at a position of three-tenths of the thickness of the steel sheet is less than 10° C./s, the above effects are not recognized.
• the average cooling rate of the surface layer ⁇ the average cooling rate at the position of three-tenths of the thickness of the steel sheet is 10° C./s or more.
• the average cooling rate is determined by (temperature at the start of cooling ⁇ temperature at the end of cooling)/cooling time.
• the temperature of the surface layer is actually measured with a thermometer.
• the temperature at the position of three-tenths of the thickness of the steel sheet is determined by calculating the temperature distribution in a cross section of the steel sheet by heat transfer analysis and correcting the result by the actual temperature of the surface of the steel sheet.
• forced cooling may be performed at the average cooling rate.
• the cooling method is preferably, but not limited to, water cooling, for example.
• the cooling stop temperature is Trs or more and (Trs+250° C.) or less.
• Trs cooling stop temperature
• the microstructure becomes tempered martensite or lower bainite. Both tempered martensite and lower bainite have a high-strength microstructure but have significantly low uniform elongation.
• the cooling stop temperature is Trs or more.
• Trs+250° C. ferrite is formed, and the tensile strength of 980 MPa cannot be achieved.
• the cooling stop temperature is (Trs+250° C.) or less.
• Trs is defined by the formula (3):
• Trs (° C.) 500 ⁇ 450 ⁇ C— 35 ⁇ Mn ⁇ 15 ⁇ Cr— 10 ⁇ Ni ⁇ 20 ⁇ Mo (3)
• the hot-rolled steel sheet after the cooling is coiled under the condition of a coiling temperature: Trs or more and (Trs+250° C.) or less.
• Trs a coiling temperature
• Trs+250° C. a coiling temperature above (Trs+250° C.)
• ferrite is formed, and the tensile strength of 980 MPa cannot be achieved.
• the coiling temperature is (Trs+250° C.) or less.
• cooling to 100° C. or less is further performed at an average cooling rate of 20° C./s or less (second cooling).
• the average cooling rate has an influence on the formation of fresh martensite and/or retained austenite.
• the average cooling rate is 20° C./s or less, preferably 2° C./s or less, more preferably 0.02° C./s or less.
• the lower limit of the average cooling rate is preferably, but not limited to, 0.0001° C./s or more.
• the cooling can be performed to any temperature of 100° C. or less, preferably in the range of approximately 10° C. to 30° C. (for example, room temperature).
• the cooling may be performed in any form, for example, in the state of a coil.
• a high-strength steel sheet according to aspects of the present invention can be manufactured in accordance with the procedure described above.
• the coiling and the subsequent cooling may be followed by routine procedures. For example, temper rolling may be performed, or pickling may be performed to remove scales formed on the surface.
• a molten steel with the composition shown in Table 1 was obtained by steelmaking in a converter, and a steel slab as a steel material was manufactured by a continuous casting method.
• the steel material was heated to the heating temperature shown in Table 2, and the steel material after the heating was then subjected to hot rolling including rough rolling and finish rolling to manufacture a hot-rolled steel sheet.
• the finishing temperature in the hot rolling was shown in Table 2.
• the hot-rolled steel sheet was cooled under the conditions of the average cooling rate and the cooling stop temperature shown in Table 2 (first cooling).
• the hot-rolled steel sheet after the cooling was coiled at the coiling temperature shown in Table 2, and the coiled steel sheet was cooled at the average cooling rate shown in Table 2 (second cooling) to manufacture a high-strength steel sheet.
• the cooling was followed by skin pass rolling and pickling as post-treatment. The pickling was performed at a temperature of 85° C. using aqueous hydrochloric acid with a concentration of 10% by mass.
• a test specimen was taken from the high-strength steel sheet, and the microstructure, surface roughness, and mechanical properties were evaluated in accordance with the following procedures.
• test specimen for microstructure observation was taken from the high-strength steel sheet such that a thickness cross section parallel to the rolling direction was an observation surface.
• the surface of the test specimen was polished and was corroded with a corrosive liquid (3% by volume nital solution) to expose the microstructure.
• a surface layer region extending from the surface of the test specimen to a position of one-tenth of the thickness of the steel sheet and an inner region extending from the position of one-tenth to a position of three-tenths of the thickness of the steel sheet were then photographed with a scanning electron microscope (SEM) at a magnification of 5000 times in 10 visual fields to acquire a SEM image of the microstructure.
• SEM image was analyzed by image processing to quantify the area ratios of upper bainite (UB), polygonal ferrite (F), and tempered martensite (TM).
• a sample for hardness measurement was taken from the high-strength steel sheet such that a thickness cross section parallel to the rolling direction was a hardness measurement cross section.
• the hardness was measured in a surface layer region extending from the surface of the steel sheet to a position of one-tenth of the thickness of the steel sheet and in an inner region extending from the position of one-tenth to a position of three-tenths of the thickness of the steel sheet.
• the hardness of the surface layer region extending from the surface of the steel sheet to the position of one-tenth of the thickness of the steel sheet was measured at an indentation distance of 250 ⁇ m at a position away from the surface by 50 ⁇ m.
• the hardness of the inner region extending from the position of one-tenth to the position of three-tenths of the thickness of the steel sheet was measured at an indentation distance of 250 ⁇ m at a position of one-fifth of the thickness of the steel sheet.
• the hardness measurement conditions included a load of 100 g, a holding time of 10 seconds, and averaging at five points of measurement.
• a JIS No. 5 test specimen (gauge length (GL): 50 mm) was taken from the high-strength steel sheet such that the tensile direction was perpendicular to the rolling direction.
• the test specimen was subjected to a tensile test in accordance with JIS Z 2241 to determine the yield strength (yield point, YP), tensile strength (TS), yield ratio (YR), total elongation (El), and uniform elongation (u-E1).
• the tensile test of each high-strength steel sheet was performed twice, and the average of the measured values is shown in Table 3 as the mechanical characteristics of the high-strength steel sheet.
• a TS of 980 MPa or more was rated as high strength.
• a uniform elongation of 6% or more was rated as high press formability.
• a bending test was performed in accordance with JIS Z 2248 (2014) (a V block 90-degree V bending test) on a test specimen with a rectangular shape of 100 mm ⁇ 35 mm, which was taken from the hot-rolled steel sheet at a 1 ⁇ 2 position in the width direction such that the longitudinal direction of the test specimen was perpendicular to the rolling direction.
• the bending punch radius R ranged in 0.5 mm increments from 0.5 mm to 2.0 times or more of the thickness of the steel sheet t.
• To determine the presence and depth of a flex crack the test specimen after the bending test was cut at three positions of a quarter, half, and three quarters of the width of the test specimen in a plane parallel to the longitudinal direction of the test specimen and perpendicular to the surface of the test specimen.
• the cross-sections were mirror-polished, and a crack outside and inside the bend of the test specimen was observed with an optical microscope to measure the maximum crack depth outside and inside the bend in the three cross-sections, thereby determining the critical bending radius (minimum bending radius) at which the crack depth outside and inside the bend was less than 50 ⁇ m. R/t of 1.5 or less was judged to be acceptable.
• a crack of 50 ⁇ m or more outside or inside the bend at a critical bending radius of 2.0 times or more of the thickness t is considered to indicate low bendability, and the critical bending radius R is not determined.

Landscapes

• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Mechanical Engineering (AREA)
• Materials Engineering (AREA)
• Metallurgy (AREA)
• Organic Chemistry (AREA)
• Physics & Mathematics (AREA)
• Thermal Sciences (AREA)
• Crystallography & Structural Chemistry (AREA)
• Heat Treatment Of Sheet Steel (AREA)
• Shaping Metal By Deep-Drawing, Or The Like (AREA)
• Bending Of Plates, Rods, And Pipes (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=83458933

Family Applications (1)

Country Status (7)

Family Cites Families (11)

• 2022
  • 2022-03-15 MX MX2023011353A patent/MX2023011353A/es unknown
  • 2022-03-15 CN CN202280023929.9A patent/CN117043381A/zh active Pending
  • 2022-03-15 JP JP2022543074A patent/JP7168137B1/ja active Active
  • 2022-03-15 EP EP22780060.4A patent/EP4282993A4/fr active Pending
  • 2022-03-15 WO PCT/JP2022/011493 patent/WO2022209839A1/fr active Application Filing
  • 2022-03-15 KR KR1020237032361A patent/KR20230148352A/ko active Search and Examination
  • 2022-03-15 US US18/282,304 patent/US20240158881A1/en active Pending

Also Published As

Similar Documents

Legal Events