HIGH STRENGTH STEEL SHEET AND METHOD FOR MANUFACTURING THE SAME

Abstract
A high strength steel sheet having 980 MPa or higher tensile strength and 10% or more elongation and a method for manufacturing the same are disclosed. The high strength steel sheet has a specific chemical composition and is such that in a region at ¼ sheet thickness, the area fraction of martensite is 60% or more, the volume fraction of retained austenite is 3% or more and 15% or less, the area fraction of the total of ferrite and bainitic ferrite is more than 10%, and the average of the proportions of packets having the largest area in prior austenite grains is 70% by area or less of the prior austenite grain.
Description
FIELD OF THE INVENTION

The present invention relates to a high strength steel sheet excellent in tensile strength, El, toughness, flatness in the width direction, and working embrittlement resistance, and to a method for manufacturing the same. The high strength steel sheet according to aspects of the present invention may be suitably used as structural members, such as automobile parts.


BACKGROUND OF THE INVENTION

Steel sheets for automobiles are being increased in strength in order to reduce CO2 emissions by weight reduction of vehicles and to enhance crashworthiness by weight reduction of automobile bodies at the same time, with introduction of new laws and regulations one after another. To increase the strength of automobile bodies, high strength steel sheets having a tensile strength (TS) of 980 MPa or higher grade are increasingly applied to principal structural parts of automobiles.


High strength steel sheets used in automobiles require excellent press formability. For example, high strength steel sheets with high El are suitably applied to automobile frame parts, such as bumpers. From the point of view of crash safety, excellent toughness and working embrittlement resistance are required.


Furthermore, high strength steel sheets used in automobiles require high flatness. Patent Literature 1 describes that warpage of a steel sheet causes operational troubles in forming lines and adversely affects the dimensional accuracy of products. The present inventors carried out extensive studies and have found that the dimensional accuracy of products is affected not only by the warpage of steel sheets but also by the flatness in the width direction that is evaluated as steepness. For example, the steepness in the width direction is suitably 0.02 or less in order to achieve excellent dimensional accuracy.


To meet the above demands, for example, Patent Literature 2 provides a high strength steel sheet having a tensile strength of 1100 MPa or more and being excellent in YR, surface quality, and weldability, and a method for manufacturing the same. However, the technique described in Patent Literature 2 does not take into consideration El, toughness, flatness in the width direction, and working embrittlement resistance.


Patent Literature 3 provides a hot-dip galvanized steel sheet with excellent press formability and low-temperature toughness that has a tensile strength of 980 MPa or more, and a method for manufacturing the same. While the steel sheet of Patent Literature 3 is improved in embrittlement at low temperatures, the technique does not take into consideration the working embrittlement of the steel sheet or the flatness in the width direction.


PATENT LITERATURE





    • PTL 1: Japanese Patent No. 4947176

    • PTL 2: Japanese Patent No. 6525114

    • PTL 3: Japanese Patent No. 6777272





Non Patent Literature





    • NPL 1: Journal of Smart Processing, 2013, Vol. 2, No. 3, pp. 110-118





SUMMARY OF THE INVENTION

Aspects of the present invention have been developed in view of the circumstances discussed above. Objects of aspects of the present invention are therefore to provide a high strength steel sheet having 980 MPa or higher TS and 10% or more El and being excellent in toughness, flatness in the width direction, and working embrittlement resistance; and to provide a method for manufacturing the same.


The present inventors carried out extensive studies directed to solving the problems described above and have consequently found the following facts.

    • (1) 980 MPa or higher TS can be realized by limiting the area fraction of martensite to 60% or more.
    • (2) 10% or more El can be achieved by limiting the volume fraction of retained austenite to 3% or more and the area fraction of the total of ferrite and bainitic ferrite to more than 10%.
    • (3) Excellent toughness can be realized by limiting the volume fraction of retained austenite to 3% or more.
    • (4) Excellent working embrittlement resistance can be achieved by limiting the proportion of a packet having the largest area in a prior austenite grain to 70% by area or less on average.
    • (5) Excellent working embrittlement resistance can be realized by limiting the volume fraction of retained austenite to 15% or less and by limiting the proportion of a packet having the largest area in a prior austenite grain to 70% by area or less on average.


Aspects of the present invention have been made based on the above findings. Specifically, a summary of aspects of the present invention is as follows.

    • [1] A high strength steel sheet having a chemical composition including, in mass %, C: 0.030% or more and 0.500% or less, Si: 0.50% or more and 2.50% or less, Mn: 1.00% or more and 5.00% or less, P: 0.100% or less, S: 0.0200% or less, Al: 1.000% or less, N: 0.0100% or less, and O: 0.0100% or less, a balance being Fe and incidental impurities, the high strength steel sheet being such that in a region at ¼ sheet thickness, an area fraction of martensite is 60% or more, a volume fraction of retained austenite is 3% or more and 15% or less, an area fraction of a total of ferrite and bainitic ferrite is more than 10%, and an average of proportions of packets having the largest area in prior austenite grains is 70% by area or less of the prior austenite grain.
    • [2] The high strength steel sheet according to [1], wherein the chemical composition further includes at least one element selected from, in mass %, 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, Co: 0.010% or less, Ni: 1.00% 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 high strength steel sheet according to [1] or [2], which has a coated layer on a surface of the steel sheet.
    • [4] A method for manufacturing the high strength steel sheet according to [1] or [2], the method including providing a cold rolled steel sheet produced by subjecting a steel having the chemical composition to hot rolling, pickling, and cold rolling; annealing the steel sheet by heating at an annealing temperature Ta of 700° C. or above and 900° C. or below for a holding time at the annealing temperature Ta of 10 seconds or more and 1000 seconds or less; bending and unbending the steel sheet 1 to 15 times in total with a roll having a radius of 800 mm or less during the annealing; cooling the steel sheet at an average cooling rate of 20° C./s or more in a temperature range from 700° C. to 600° C. and at an average cooling rate of less than 20° C./s in a temperature range from 499° C. to Ms; bending and unbending the steel sheet in the temperature range from 499° C. to Ms, 1 to 15 times in total with a roll having a radius of 800 mm or less; cooling the steel sheet at an average cooling rate of 150° C./s or less in a temperature range from Ms to a cooling stop temperature Tb; applying a tension to the steel sheet in the temperature range from Ms to the cooling stop temperature Tb while controlling the tension to 5 MPa or more and 100 MPa or less, the cooling stop temperature Tb being 100° C. or above and (Ms−80° C.) or below where Ms is a martensite start temperature (° C.) defined by formula (1); and tempering the steel sheet at a tempering temperature of Tb or above and 450° C. or below for a holding time at the tempering temperature of 10 seconds or more and 1000 seconds or less,









Ms
=

519
-

474
×

[

%


C

]


-

30.4
×

[

%


Mn

]


-

12.1
×

[

%


Cr

]


-

7.5
×

[

%


Mo

]


-

17.7
×

[

%


Ni

]


-

Ta
/
80






(
1
)







wherein [% C], [% Mn], [% Cr], [% Mo], and [% Ni] indicate the contents (mass %) of C, Mn, Cr, Mo, and Ni, respectively, and are zero when the element is absent.

    • [5] The method for manufacturing the high strength steel sheet according to [4], further including performing a coating treatment.


According to aspects of the present invention, a high strength steel sheet can be obtained that has 980 MPa or higher TS and 10% or more El and excels in toughness, flatness in the width direction, and working embrittlement resistance. Furthermore, for example, the high strength steel sheet according to aspects of the present invention may be applied to automobile structural members to reduce the weight of automobile bodies and thereby to enhance fuel efficiency. Thus, aspects of the present invention are highly valuable in industry.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a set of views illustrating a structure of a packet having the largest area in a prior austenite grain according to an embodiment of the present invention, and how the proportion of the packet is calculated.



FIG. 2 is a set of views illustrating the concept of the steepness λ in the width direction of a steel sheet according to an embodiment of the present invention, and how the steepness is calculated.





DETAILED DESCRIPTION OF EMBODIMENTS OF THE INVENTION

Embodiments of the present invention will be described below.


First, appropriate ranges of the chemical composition of the high strength steel sheet and the reasons why the chemical composition is thus limited will be described. In the following description, “%” indicating the contents of constituent elements of steel means “mass %” unless otherwise specified.


[C: 0.030% or More and 0.500% or Less]

Carbon is one of the important basic components of steel. Particularly in accordance with aspects of the present invention, carbon is an important element that affects the amount of martensite. When the C content is less than 0.030%, the amount of martensite is so small that realizing 980 MPa or higher TS is difficult. When, on the other hand, the C content is more than 0.500%, martensite becomes brittle to cause deterioration in toughness and working embrittlement resistance. Thus, the C content is limited to 0.030% or more and 0.500% or less. The lower limit of the C content is preferably 0.050% or more. The upper limit of the C content is preferably 0.400% or less. The lower limit of the C content is more preferably 0.100% or more. The upper limit of the C content is more preferably 0.350% or less.


[Si: 0.50% or More and 2.50% or Less]

Silicon is one of the important basic components of steel and is an important element that affects TS and the amount of retained austenite. When the Si content is less than 0.50%, the strength of martensite decreases to make it difficult to achieve 980 MPa or higher TS. When, on the other hand, the Si content is more than 2.50%, the amount of retained austenite is increased excessively, and toughness and working embrittlement resistance are lowered. Thus, the Si content is limited to 0.50% or more and 2.50% or less. The lower limit of the Si content is preferably 0.55% or more. The upper limit of the Si content is preferably 2.00% or less. The lower limit of the Si content is more preferably 0.60% or more. The upper limit of the Si content is more preferably 1.80% or less.


[Mn: 1.00% or More and 5.00% or Less]

Manganese is one of the important basic components of steel and is an important element that affects the amount of martensite. When the Mn content is less than 1.00%, the amount of martensite is so small that realizing 980 MPa or higher TS is difficult. When, on the other hand, the Mn content is more than 5.00%, martensite becomes brittle to cause deterioration in toughness and working embrittlement resistance. Thus, the Mn content is limited to 1.00% or more and 5.00% or less. The lower limit of the Mn content is preferably 1.50% or more. The upper limit of the Mn content is preferably 4.50% or less. The lower limit of the Mn content is more preferably 2.00% or more. The upper limit of the Mn content is more preferably 4.00% or less.


[P: 0.100% or Less]

Phosphorus is segregated at prior austenite grain boundaries and makes the grain boundaries brittle, thereby lowering the ultimate deformability of steel sheets and causing deterioration in toughness and working embrittlement resistance. Thus, the P content needs to be 0.100% or less. The lower limit of the P content is not particularly specified. In view of the fact that phosphorus is a solid solution strengthening element and can increase the strength of steel sheets, the lower limit is preferably 0.001% or more. For the reasons above, the P content is limited to 0.100% or less. The lower limit of the P content is preferably 0.001% or more. The upper limit of the P content is preferably 0.070% or less.


[S: 0.0200% or Less]

Sulfur forms sulfides and lowers the ultimate deformability of steel sheets to cause deterioration in toughness and working embrittlement resistance. Thus, the S content needs to be 0.0200% or less. The lower limit of the S content is not particularly specified but is preferably 0.0001% or more due to production technique limitations. For the reasons above, the S content is limited to 0.0200% or less. The lower limit of the S content is preferably 0.0001% or more. The upper limit of the S content is preferably 0.0050% or less.


[Al: 1.000% or Less]

Aluminum forms the oxide and lowers the ultimate deformability of steel sheets to cause deterioration in toughness and working embrittlement resistance. Thus, the Al content needs to be 1.000% or less. The lower limit of the Al content is not particularly specified. In view of the fact that aluminum suppresses the occurrence of carbides during continuous annealing and promotes the formation of retained austenite, the Al content is preferably 0.001% or more. For the reasons above, the Al content is limited to 1.000% or less. The lower limit of the Al content is preferably 0.001% or more. The upper limit of the Al content is preferably 0.500% or less.


[N: 0.0100% or Less]

Nitrogen forms nitrides and lowers the ultimate deformability of steel sheets to cause deterioration in toughness and working embrittlement resistance. Thus, the N content needs to be 0.0100% or less. The lower limit of the N content is not particularly specified but the N content is preferably 0.0001% or more due to production technique limitations. For the reasons above, the N content is limited to 0.0100% or less. The lower limit of the N content is preferably 0.0001% or more. The upper limit of the N content is preferably 0.0050% or less.


[O: 0.0100% or Less]

Oxygen forms oxides and lowers the ultimate deformability of steel sheets to cause deterioration in toughness and working embrittlement resistance. Thus, the O content needs to be 0.0100% or less. The lower limit of the O content is not particularly specified but the O content is preferably 0.0001% or more due to production technique limitations. For the reasons above, the O content is limited to 0.0100% or less. The lower limit of the O content is preferably 0.0001% or more. The upper limit of the O content is preferably 0.0050% or less.


The chemical composition of the high strength steel sheet according to an embodiment of the present invention includes the components described above, and the balance is Fe and incidental impurities. Here, the incidental impurities include Zn, Pb, As, Ge, Sr, and Cs. A total of 0.100% or less of these impurities is acceptable.


In addition to the components in the proportions described above, the high strength steel sheet according to aspects of the present invention may further include at least one element selected from, in mass %, 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. These elements may be contained singly or in combination.


When the contents of Ti, Nb, and V are each 0.200% or less, coarse precipitates and inclusions will not occur in large amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the contents of Ti, Nb, and V are each preferably 0.200% or less. The lower limits of the contents of Ti, Nb, and V are not particularly specified. These elements form fine carbides, nitrides, or carbonitrides during hot rolling or continuous annealing to increase the strength of steel sheets. In view of this fact, the contents of Ti, Nb, and V are each more preferably 0.001% or more. When titanium, niobium, and vanadium are added, the contents thereof are each limited to 0.200% or less for the reasons above. The lower limits of the contents of Ti, Nb, and V, when added, are each more preferably 0.001% or more. The upper limits of the contents of Ti, Nb, and V, when added, are each more preferably 0.100% or less.


When the contents of Ta and W are each 0.10% or less, coarse precipitates and inclusions will not occur in large amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the contents of Ta and W are each preferably 0.10% or less. The lower limits of the contents of Ta and W are not particularly specified. These elements form fine carbides, nitrides, or carbonitrides during hot rolling or continuous annealing to increase the strength of steel sheets. In view of this fact, the contents of Ta and W are each more preferably 0.01% or more. When tantalum and tungsten are added, the contents thereof are each limited to 0.10% or less for the reasons above. The lower limits of the contents of Ta and W, when added, are each more preferably 0.01% or more. The upper limits of the contents of Ta and W, when added, are each more preferably 0.08% or less.


When the B content is 0.0100% or less, inner cracks that lower the ultimate deformability of steel sheets will not form during casting or hot rolling and thus there will be no deterioration in toughness or working embrittlement resistance. Thus, the B content is preferably 0.0100% or less. The lower limit of the B content is not particularly specified. The B content is more preferably 0.0003% or more in view of the fact that this element is segregated at austenite grain boundaries during annealing and enhances hardenability. When boron is added, the content thereof is limited to 0.0100% or less for the reasons above. The lower limit of the content of B, when added, is more preferably 0.0003% or more. The upper limit of the content of B, when added, is more preferably 0.0080% or less.


When the contents of Cr, Mo, and Ni are each 1.00% or less, coarse precipitates and inclusions will not occur in increased amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the contents of Cr, Mo, and Ni are each preferably 1.00% or less. The lower limits of the contents of Cr, Mo, and Ni are not particularly specified. In view of the fact that these elements enhance hardenability, the contents of Cr, Mo, and Ni are each more preferably 0.01% or more. When chromium, molybdenum, and nickel are added, the contents thereof are each limited to 1.00% or less for the reasons above. The lower limits of the contents of Cr, Mo, and Ni, when added, are each more preferably 0.01% or more. The upper limits of the contents of Cr, Mo, and Ni, when added, are each more preferably 0.80% or less.


When the Co content is 0.010% or less, coarse precipitates and inclusions will not occur in increased amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the Co content is preferably 0.010% or less. The lower limit of the Co content is not particularly specified. In view of the fact that this element enhances hardenability, the Co content is more preferably 0.001% or more. When cobalt is added, the content thereof is limited to 0.010% or less for the reasons above. The lower limit of the content of Co, when added, is more preferably 0.001% or more. The upper limit of the content of Co, when added, is more preferably 0.008% or less.


When the Cu content is 1.00% or less, coarse precipitates and inclusions will not occur in increased amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the Cu content is preferably 1.00% or less. The lower limit of the Cu content is not particularly specified. In view of the fact that this element enhances hardenability, the Cu content is preferably 0.01% or more. When copper is added, the content thereof is limited to 1.00% or less for the reasons above. The lower limit of the content of Cu, when added, is more preferably 0.01% or more. The upper limit of the content of Cu, when added, is more preferably 0.80% or less.


When the Sn content is 0.200% or less, inner cracks that lower the ultimate deformability of steel sheets will not form during casting or hot rolling and thus there will be no deterioration in toughness or working embrittlement resistance. Thus, the Sn content is preferably 0.200% or less. The lower limit of the Sn content is not particularly specified. The Sn content is more preferably 0.001% or more in view of the fact that tin enhances hardenability (in general, is an element that enhances corrosion resistance). When tin is added, the content thereof is limited to 0.200% or less for the reasons above. The lower limit of the content of Sn, when added, is more preferably 0.001% or more. The upper limit of the content of Sn, when added, is more preferably 0.100% or less.


When the Sb content is 0.200% or less, coarse precipitates and inclusions will not occur in increased amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the Sb content is preferably 0.200% or less. The lower limit of the Sb content is not particularly specified. In view of the fact that this element enables control of the thickness of surface layer softening and the strength, the Sb content is more preferably 0.001% or more. When antimony is added, the content thereof is limited to 0.200% or less for the reasons above. The lower limit of the content of Sb, when added, is more preferably 0.001% or more. The upper limit of the content of Sb, when added, is more preferably 0.100% or less.


When the contents of Ca, Mg, and REM are each 0.0100% or less, coarse precipitates and inclusions will not occur in increased amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the contents of Ca, Mg, and REM are each preferably 0.0100% or less. The lower limits of the contents of Ca, Mg, and REM are not particularly specified. In view of the fact that these elements change the shapes of nitrides and sulfides into spheroidal and enhance the ultimate deformability of steel sheets, the contents of Ca, Mg, and REM are each more preferably 0.0005% or more. When calcium, magnesium, and rare earth metal(s) are added, the contents thereof are each limited to 0.0100% or less for the reasons above. The lower limits of the contents of Ca, Mg, and REM, when added, are each more preferably 0.0005% or more. The upper limits of the contents of Ca, Mg, and REM, when added, are each more preferably 0.0050% or less.


When the contents of Zr and Te are each 0.100% or less, coarse precipitates and inclusions will not occur in increased amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the contents of Zr and Te are each preferably 0.100% or less. The lower limits of the contents of Zr and Te are not particularly specified. In view of the fact that these elements change the shapes of nitrides and sulfides into spheroidal and enhance the ultimate deformability of steel sheets, the contents of Zr and Te are each more preferably 0.001% or more. When zirconium and tellurium are added, the contents thereof are each limited to 0.100% or less for the reasons above. The lower limits of the contents of Zr and Te, when added, are each more preferably 0.001% or more. The upper limits of the contents of Zr and Te, when added, are each more preferably 0.080% or less.


When the Hf content is 0.10% or less, coarse precipitates and inclusions will not occur in increased amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the Hf content is preferably 0.10% or less. The lower limit of the Hf content is not particularly specified. In view of the fact that this element changes the shapes of nitrides and sulfides into spheroidal and enhances the ultimate deformability of steel sheets, the Hf content is more preferably 0.01% or more. When hafnium is added, the content thereof is limited to 0.10% or less for the reasons above. The lower limit of the content of Hf, when added, is more preferably 0.01% or more. The upper limit of the content of Hf, when added, is more preferably 0.08% or less.


When the Bi content is 0.200% or less, coarse precipitates and inclusions will not occur in increased amounts and thus will not cause lowering of the ultimate deformability of steel sheets; hence there will be no deterioration in toughness or working embrittlement resistance. Thus, the Bi content is preferably 0.200% or less. The lower limit of the Bi content is not particularly specified. In view of the fact that this element reduces the occurrence of segregation, the Bi content is more preferably 0.001% or more. When bismuth is added, the content thereof is limited to 0.200% or less for the reasons above. The lower limit of the content of Bi, when added, is more preferably 0.001% or more. The upper limit of the content of Bi, when added, is more preferably 0.100% or less.


When the content of any of Ti, Nb, V, Ta, W, B, Cr, Mo, Ni, Co, Cu, Sn, Sb, Ca, Mg, REM, Zr, Te, Hf, and Bi is below the preferred lower limit, the element does not impair the advantageous effects according to aspects of the present invention and is regarded as an incidental impurity.


Next, the steel microstructure of the high strength steel sheet according to aspects of the present invention will be described.


[Area Fraction of Martensite: 60% or More]

This configuration is a very important requirement that constitutes an aspect of the present invention. 980 MPa or higher TS can be achieved when the area fraction of martensite is 60% or more. Thus, the area fraction of martensite is limited to 60% or more. The area fraction is preferably 62% or more, and more preferably 64% or more.


[Volume Fraction of Retained Austenite: 3% or More and 15% or Less]

This configuration is a very important requirement that constitutes an aspect of the present invention. When the volume fraction of retained austenite is less than 3%, it is difficult to realize 10% or more El and it is also difficult to attain excellent toughness because the toughness enhancement effect by retained austenite cannot be obtained. When the amount of retained austenite is more than 15%, retained austenite is excessively transformed into hard martensite at the time of working and the steel sheet is lowered in ultimate deformability and will not attain excellent working embrittlement resistance. Thus, the retained austenite is limited to 3% or more and 15% or less. The lower limit of the amount of retained austenite is preferably 5% or more. The upper limit of the amount of retained austenite is preferably 14% or less. The lower limit of the amount of retained austenite is more preferably 7% or more. The upper limit of the amount of retained austenite is more preferably 13% or less.


Here, retained austenite is measured as follows. The steel sheet is polished to expose a face 0.1 mm below ¼ sheet thickness and is thereafter further chemically polished to expose a face 0.1 mm below the face exposed above. The face is analyzed with an X-ray diffractometer using CoKα radiation to determine the integral intensity ratios of the diffraction peaks of {200}, {220}, and {311} planes of fcc iron and {200}, {211}, and {220} planes of bcc iron. Nine integral intensity ratios thus obtained are averaged to determine retained austenite.


[Area Fraction of the Total of Ferrite and Bainitic Ferrite: More than 10%]


This configuration is a very important requirement that constitutes an aspect of the present invention. When the total amount of ferrite and bainitic ferrite is 10% or less, it is difficult to achieve 10% or more El. Thus, the total amount of ferrite and bainitic ferrite is limited to more than 10%. The total amount is preferably 12% or more, and more preferably 13% or more. The upper limit of the total amount of ferrite and bainitic ferrite is not particularly limited.


Here, the total amount of ferrite and bainitic ferrite is measured as follows. A longitudinal cross section of the steel sheet is polished and is etched with 3 vol % Nital. A portion at ¼ sheet thickness (a location corresponding to ¼ of the sheet thickness in the depth direction from the steel sheet surface) is observed using SEM in 10 fields of view at a magnification of ×2000. In the microstructure images, ferrite and bainitic ferrite are recessed structures having a flat interior and containing no inner carbides. The values thus obtained are averaged to determine the total amount of ferrite and bainitic ferrite.


The amount of martensite is measured as follows. The amount of martensite can be determined by measuring the amounts of retained austenite, ferrite, and bainitic ferrite based on the methods described above, and subtracting the total thereof from 100%. Thus, the amount of martensite in accordance with aspects of the present invention includes both quenched martensite and tempered martensite. Because the volume fraction of retained austenite is almost equal to the area fraction, the amount is subtracted as such from 100% together with the amounts of ferrite and bainitic ferrite expressed in area fraction.


[Average of the Proportions of Packets Having the Largest Area in Prior Austenite Grains: 70% by Area or Less]

This configuration is a very important requirement that constitutes an aspect of the present invention. The proportion of a packet having the largest area in a prior austenite grain affects the flatness in the width direction and the working embrittlement resistance. As illustrated in FIG. 1, a prior austenite grain contains up to four kinds of packets distinguished by crystal habit plane formed by transformation. The packet having the largest area in a prior austenite grain is the packet that occupies the largest area among such packets.


The proportion of one packet in a prior austenite grain is determined by dividing the area of the packet of interest by the area of the whole prior austenite grain.


As a result of extensive studies, the present inventors have found that strain among the packets is reduced and the flatness in the width direction is improved by lowering the proportion of a packet having the largest area in a prior austenite grain. The present inventors have also found that lowering the proportion of a packet having the largest area in a prior austenite grain leads to a fine microstructure and suppresses crack propagation, thereby enhancing the working embrittlement resistance of the steel sheet. Thus, the average of the proportions of packets having the largest area in prior austenite grains is limited to 70% or less. The average proportion is preferably 60% or less. The lower limit of the average proportion of packets having the largest area in prior austenite grains is not particularly limited. The grains contain up to four kinds of packets. When four packets are evenly distributed, the proportion of a packet having the largest area in the prior austenite grain is 25%. Thus, the lower limit of the average proportion of packets having the largest area in prior austenite grains is preferably 25% or more. However, the lower limit of the average proportion is not necessarily limited thereto.


Here, the average proportion of packets having the largest area in prior austenite grains is measured as follows. First, a test specimen for microstructure observation is sampled from the cold rolled steel sheet. Next, the sampled test specimen is polished by vibration polishing with colloidal silica to expose a cross section in the rolling direction (a longitudinal cross section) for use as observation surface. The observation surface is specular. Next, electron backscatter diffraction (EBSD) measurement is performed with respect to a portion at ¼ sheet thickness (a location corresponding to ¼ of the sheet thickness in the depth direction from the steel sheet surface) to obtain local crystal orientation data. Here, the SEM magnification is ×1000, the step size is 0.2 μm, the measured region is 80 μm square, and the WD is 15 mm. The local orientation data obtained is analyzed with OIM Analysis 7 (OIM), and a map (a CP map) that shows close-packed plane groups (CP groups) with different colors is created using the method described in Non Patent Literature 1. In accordance with aspects of the present invention, a packet is defined as a region or regions belonging to the same CP group. From the CP map obtained, the area of the packet having the largest area is determined and is divided by the area of the whole prior austenite grain to give the proportion of the packet having the largest area in the prior austenite grain. This analysis is performed with respect to 10 or more adjacent prior austenite grains, and the results are averaged to give the average proportion of packets having the largest area in prior austenite grains.


Next, a manufacturing method according to aspects of the present invention will be described.


In accordance with aspects of the present invention, a steel material (a steel slab) may be obtained by any known steelmaking method without limitation, such as a converter or an electric arc furnace. To prevent macro-segregation, the steel slab (the slab) is preferably produced by a continuous casting method.


In accordance with aspects of the present invention, the slab heating temperature, the slab soaking holding time, and the coiling temperature in hot rolling are not particularly limited. For example, the steel slab may be hot rolled in such a manner that the slab is heated and is then rolled, that the slab is subjected to hot direct rolling after continuous casting without being heated, or that the slab is subjected to a short heat treatment after continuous casting and is then rolled. The slab heating temperature, the slab soaking holding time, the finish rolling temperature, and the coiling temperature in hot rolling are not particularly limited. The lower limit of the slab heating temperature is preferably 1100° C. or above. The upper limit of the slab heating temperature is preferably 1300° C. or below. The lower limit of the slab soaking holding time is preferably 30 minutes or more. The upper limit of the slab soaking holding time is preferably 250 minutes or less. The lower limit of the finish rolling temperature is preferably Ar3 transformation temperature or above. Furthermore, the lower limit of the coiling temperature is preferably 350° C. or above. The upper limit of the coiling temperature is preferably 650° C. or below.


The hot rolled steel sheet thus produced is pickled. Pickling can remove oxides on the steel sheet surface and is thus important to ensure good chemical convertibility and a high quality of coating in the final high strength steel sheet. Pickling may be performed at a time or several. The hot rolled sheet that has been pickled may be cold rolled directly or may be subjected to heat treatment before cold rolling.


The rolling reduction in cold rolling and the sheet thickness after rolling are not particularly limited. The lower limit of the rolling reduction is preferably 30% or more. The upper limit of the rolling reduction is preferably 80% or less. The advantageous effects according to aspects of the present invention may be obtained without any limitations on the number of rolling passes and the rolling reduction in each pass.


The cold rolled steel sheet obtained as described above is annealed. Annealing conditions are as follows.


[Annealing Temperature Ta: 700° C. or Above and 900° C. or Below]

When the annealing temperature Ta is below 700° C., the amount of martensite is so small that realizing 980 MPa or higher TS is difficult. When, on the other hand, the annealing temperature is above 900° C., the total amount of ferrite and bainitic ferrite decreases to make it difficult to achieve 10% or more El. Thus, the annealing temperature is limited to 700° C. or above and 900° C. or below. The lower limit of the annealing temperature is preferably 750° C. or above. The upper limit of the annealing temperature is preferably 870° C. or below.


[Holding Time During Annealing at the Annealing Temperature Ta: 10 Seconds or More and 1000 Seconds or Less]

When the holding time at the annealing temperature Ta is less than 10 seconds, the amount of martensite is so small that realizing 980 MPa or higher TS is difficult. When, on the other hand, the holding time at the annealing temperature Ta is more than 1000 seconds, the total amount of ferrite and bainitic ferrite decreases to make it difficult to achieve 10% or more El. Thus, the holding time at the annealing temperature Ta is limited to 10 seconds or more and 1000 seconds or less. The lower limit of the holding time at the annealing temperature Ta is preferably 50 seconds or more. The upper limit of the holding time at the annealing temperature Ta is preferably 500 seconds or less.


[During the Annealing, the Steel Sheet is Bent and Unbent 1 to 15 Times in Total with a Roll Having a Radius of 800 mm or Less.]


As a result of extensive studies, the present inventors have found that bending and unbending of the steel sheet during annealing affects the proportion of a packet having the largest area in a prior austenite grain. When the steel sheet being annealed is not subjected to bending and unbending with a roll having a radius of 800 mm or less, the amount of nucleation sites for martensite transformation is reduced. Consequently, the average proportion of packets having the largest area in prior austenite grains exceeds 70%, and the flatness in the width direction and also the working embrittlement resistance are deteriorated. When, on the other hand, the steel sheet being annealed is subjected to bending and unbending 16 times or more with a roll having a radius of 800 mm or less, the steel sheet is deteriorated in ultimate deformability and also in working embrittlement resistance. Thus, in the annealing, the total count of bending and unbending with a roll having a radius of 800 mm or less is limited to 1 or more and 15 or less. The radius of the roll is preferably 600 mm or less. The lower limit of the total count of bending and unbending is preferably 3 or more. The upper limit of the total count of bending and unbending is preferably 10 or less. The lower limit of the radius of the roll is not necessarily limited but is preferably 50 mm or more.


Incidentally, “bending and unbending” is a treatment that bends the steel sheet with a roll in one direction according to a known technique and unbends the steel sheet in the opposite direction to cancel the bend. Bending and unbending are not counted in pairs. That is, each bending is counted one and each unbending is counted one.


[Average Cooling Rate in the Temperature Range from 700° C. to 600° C.: 20° C./s or More]


As a result of extensive studies, the present inventors have found that the average cooling rate in the temperature range from 700° C. to 600° C. affects the proportion of a packet having the largest area in a prior austenite grain. When the average cooling rate in the temperature range from 700° C. to 600° C. is less than 20° C./s, the effects imparted by bending and unbending of the steel sheet during annealing are lowered and the amount of nucleation sites for martensite transformation is reduced. Consequently, the average proportion of packets having the largest area in prior austenite grains exceeds 70%, and the flatness in the width direction and also the working embrittlement resistance are deteriorated. Thus, the average cooling rate from 700° C. to 600° C. is limited to 20° C./s or more and is preferably 30° C./s or more. The upper limit is not necessarily limited but is preferably 100° C./s or less.


[Average Cooling Rate in the Temperature Range from 499° C. to Ms: Less than 20° C./s]


The average cooling rate in the temperature range from 499° C. to Ms affects the total area fraction of ferrite and bainitic ferrite. When the average cooling rate in the temperature range from 499° C. to Ms is 20° C./s or more, the total amount of ferrite and bainitic ferrite decreases to make it difficult to achieve 10% or more El. Thus, the average cooling rate in the temperature range from 499° C. to Ms is limited to less than 20° C./s. The average cooling rate is preferably 18° C./s or less. The lower limit is not necessarily limited but is preferably 5° C./s or more.


The martensite start temperature Ms (° C.) is defined by the following formula (1):









Ms
=

519
-

474
×

[

%


C

]


-

30.4
×

[

%


Mn

]


-

12.1
×

[

%


Cr

]


-

7.5
×

[

%


Mo

]


-

17.7
×

[

%


Ni

]


-

Ta
/
80






(
1
)







wherein [% C], [% Mn], [% Cr], [% Mo], and [% Ni] indicate the contents (mass %) of C, Mn, Cr, Mo, and Ni, respectively, and are zero when the element is absent.


[The Steel Sheet in the Temperature Range from 499° C. to Ms is Bent and Unbent 1 to 15 Times in Total with a Roll Having a Radius of 800 mm or Less.]


As a result of extensive studies, the present inventors have found that bending and unbending of the steel sheet in the temperature range from 499° C. to Ms affects the proportion of a packet having the largest area in a prior austenite grain. When the steel sheet in the temperature range from 499° C. to Ms is not subjected to bending and unbending with a roll having a radius of 800 mm or less, the amount of martensite nucleation sites is reduced. Consequently, the average proportion of packets having the largest area in prior austenite grains exceeds 70%, and the flatness in the width direction and also the working embrittlement resistance are deteriorated. When, on the other hand, the steel sheet in the temperature range from 499° C. to Ms is subjected to bending and unbending 16 times or more with a roll having a radius of 800 mm or less, the steel sheet is deteriorated in ultimate deformability and also in working embrittlement resistance. Thus, the total count of bending and unbending in the temperature range from 499° C. to Ms with a roll having a radius of 800 mm or less is limited to 1 or more and 15 or less. The radius of the roll is preferably 600 mm or less. The lower limit of the total count of bending and unbending is preferably 3 or more. The upper limit of the total count of bending and unbending is preferably 10 or less. The lower limit of the radius of the roll is not necessarily limited but is preferably 50 mm or more.


[Average Cooling Rate in the Temperature Range from Ms to Cooling Stop Temperature Tb: 150° C./s or Less]


As a result of extensive studies, the present inventors have found that the average cooling rate in the temperature range from Ms to the cooling stop temperature Tb affects the proportion of a packet having the largest area in a prior austenite grain. When the average cooling rate in the temperature range from Ms to the cooling stop temperature Tb is more than 150° C./s, the martensite transformation rate is so fast that a packet grows fast easily. Consequently, the average proportion of packets having the largest area in prior austenite grains exceeds 70%, and the flatness in the width direction and also the working embrittlement resistance are deteriorated. Thus, the average cooling rate in the temperature range from Ms to the cooling stop temperature Tb is limited to 150° C./s or less. The average cooling rate is preferably 120° C./s or less. The lower limit is not necessarily limited but is preferably 5° C./s or more.


[Tension Applied to the Steel Sheet in the Temperature Range from Ms to the Cooling Stop Temperature Tb: 5 MPa or More and 100 MPa or Less]


As a result of extensive studies, the present inventors have found that the application of tension to the steel sheet in the temperature range from Ms to the cooling stop temperature Tb affects the proportion of a packet having the largest area in a prior austenite grain. When the tension applied to the steel sheet in the temperature range from Ms to the cooling stop temperature Tb is less than 5 MPa, the amount of martensite nucleation sites is reduced. Consequently, the average proportion of packets having the largest area in prior austenite grains exceeds 70%, and the flatness in the width direction and also the working embrittlement resistance are deteriorated. When, on the other hand, more than 100 MPa tension is applied to the steel sheet in the temperature range from Ms to the cooling stop temperature Tb, the total amount of ferrite and bainitic ferrite is excessively increased and thus the amount of martensite decreases to make it difficult to realize 980 MPa or higher TS. Thus, the tension applied to the steel sheet in the temperature range from Ms to the cooling stop temperature Tb is limited to 5 MPa or more and 100 MPa or less. The lower limit of the tension applied to the steel sheet in the temperature range from Ms to the cooling stop temperature Tb is preferably 6 MPa or more. The upper limit of the tension applied to the steel sheet in the temperature range from Ms to the cooling stop temperature Tb is preferably 50 MPa or less. The tension is applied in a usual manner. As an example, the tension may be applied by controlling the roll speeds of the rolls in the furnace.


While the bending and unbending process increases the number of nucleation sites that are martensite start sites, the tension application process produces different effects by promoting martensite transformation itself.


[Cooling Stop Temperature Tb: 100° C. or Above and (Ms−80° C.) or Below]

When the cooling stop temperature Tb is below 100° C., the amount of retained austenite decreases and bendability is lowered. When, on the other hand, the cooling stop temperature Tb is above (Ms−80° C.), the amount of retained austenite is excessively increased and the prior austenite grain size is excessively enlarged to cause deterioration in working embrittlement resistance. Thus, the cooling stop temperature Tb is limited to 100° C. or above and (Ms−80° C.) or below. The lower limit of the cooling stop temperature Tb is preferably 120° C. or above. The upper limit of the cooling stop temperature Tb is preferably (Ms−100° C.) or below.


[Tempering Temperature: Tb or Above and 450° C. or Below]

After the cooling is stopped at the cooling stop temperature Tb, the steel sheet is held at the temperature or is reheated and held at a temperature of 450° C. or below to stabilize retained austenite. When the tempering temperature is below Tb, retained austenite cannot be obtained as desired; consequently El is lowered and excellent toughness is hardly obtained. When the tempering temperature is above 450° C., martensite is excessively tempered to make it difficult to achieve 980 MPa or higher TS. Thus, the tempering temperature is limited to Tb or above and 450° C. or below. The lower limit of the tempering temperature is preferably (Tb+10° C.) or above. The upper limit of the tempering temperature is preferably 420° C. or below.


[Holding Time at the Tempering Temperature: 10 Seconds or More and 1000 Seconds or Less]

When the holding time at the tempering temperature is less than 10 seconds, austenite stabilization is insufficient and retained austenite cannot be obtained as desired; consequently El is lowered and excellent toughness is hardly obtained. When the holding time at the tempering temperature is more than 1000 seconds, martensite is excessively tempered to make it difficult to achieve 980 MPa or higher TS. Thus, the holding time at the tempering temperature is limited to 10 seconds or more and 1000 seconds or less. The lower limit of the holding time at the tempering temperature is preferably 50 seconds or more. The upper limit of the holding time at the tempering temperature is preferably 800 seconds or less.


Post-temper cooling is not particularly limited and the steel sheet may be cooled to a desired temperature in an appropriate manner. Incidentally, the desired temperature is preferably about room temperature.


Furthermore, the high strength steel sheet described above may be worked under conditions where the amount of equivalent plastic strain is 0.10% or more and 5.00% or less. The working may be followed by reheating at 100° C. or above and 400° C. or below.


When the high strength steel sheet is a product that is traded, the steel sheet is usually traded after being cooled to room temperature.


The high strength steel sheet may be subjected to coating treatment during annealing or after annealing.


For example, the coating treatment during annealing may be hot-dip galvanizing treatment performed when the annealed steel sheet is being cooled or has been cooled from 700° C. to 600° C. at an average cooling rate of 20° C./s or more. The hot-dip galvanizing treatment may be followed by alloying. For example, the coating treatment after annealing may be Zn—Ni electrical alloy coating treatment or pure Zn electroplated coating treatment performed after tempering. A coated layer may be formed by electroplated coating, or hot-dip zinc-aluminum-magnesium alloy coating may be applied. While the coating treatment has been described above focusing on zinc coating, the types of coating metals, such as Zn coating and Al coating, are not particularly limited. Other conditions in the manufacturing method are not particularly limited. From the point of view of productivity, the series of treatments including annealing, hot-dip galvanizing, and alloying treatment of the coated zinc layer is preferably performed on hot-dip galvanizing line CGL (continuous galvanizing line). To control the coating weight of the coated layer, the hot-dip galvanizing treatment may be followed by wiping. Conditions for operations, such as coating, other than those conditions described above may be determined in accordance with the usual hot-dip galvanizing technique.


After the coating treatment after annealing, the steel sheet may be worked again under conditions where the amount of equivalent plastic strain is 0.10% or more and 5.00% or less. The working may be followed by reheating at 100° C. or above and 400° C. or below.


EXAMPLES

Steels having a chemical composition described in Table 1 and 2, with the balance being Fe and incidental impurities, were smelted in a converter and were continuously cast into slabs. Next, the slabs obtained were heated, hot rolled, pickled, cold rolled, and subjected to annealing treatment described in Table 3 and 4. High strength cold rolled steel sheets having a sheet thickness of 0.6 to 2.2 mm were thus obtained. During annealing, the steel sheet was subjected to bending and unbending with a roll having a radius of 300 mm. In the temperature range from 499° C. to Ms, the steel sheet was subjected to bending and unbending with a roll having a radius of 300 mm. Incidentally, some of the steel sheets were subjected to coating treatment during or after annealing.


The high strength cold rolled steel sheets obtained as described above were used as test steels. Tensile characteristics, flatness in the width direction, toughness, and working embrittlement resistance were evaluated in accordance with the following test methods.











TABLE 1








Chemical composition (mass %)






















Steels
C
Si
Mn
P
S
N
O
Al
Ti
B
Nb
Cu
Others






A
0.172
1.37
2.54
0.013
0.0014
0.005
0.005
0.039





INV. EX.


B
0.157
1.07
2.86
0.005
0.0011
0.003
0.005
0.028





INV. EX.


C
0.175
1.33
2.42
0.014
0.0007
0.004
0.002
0.031





INV. EX.


D
0.172
1.14
2.80
0.009
0.0013
0.004
0.005
0.060





INV. EX.


E
0.161
1.10
2.85
0.006
0.0012
0.006
0.007
0.049





INV. EX.


F
0.037
1.01
2.66
0.010
0.0009
0.003
0.004
0.042





INV. EX.


G

0.028

1.10
2.55
0.007
0.0006
0.006
0.007
0.023





COMP. EX.


H
0.461
1.33
2.43
0.012
0.0009
0.002
0.004
0.032





INV. EX.


I

0.505

1.38
2.83
0.011
0.0007
0.004
0.002
0.015





COMP. EX.


J
0.182
0.58
2.81
0.015
0.0006
0.005
0.002
0.037





INV. EX.


K
0.179

0.42

2.45
0.011
0.0014
0.003
0.005
0.044





COMP. EX.


L
0.180
2.34
2.64
0.008
0.0014
0.003
0.003
0.059





INV. EX.


M
0.172

2.54

2.74
0.009
0.0008
0.005
0.005
0.024





COMP. EX.


N
0.165
1.15
1.05
0.013
0.0007
0.003
0.002
0.046





INV. EX.


O
0.170
1.29

0.95

0.011
0.0013
0.005
0.006
0.025





COMP. EX.


P
0.163
1.27
4.96
0.006
0.0008
0.003
0.005
0.018





INV. EX.


Q
0.177
1.09

5.16

0.008
0.0013
0.005
0.005
0.013





COMP. EX.


R
0.171
1.14
2.73
0.097
0.0008
0.001
0.005
0.038





INV. EX.


S
0.180
1.38
2.50

0.109

0.0012
0.004
0.004
0.048





COMP. EX.


T
0.184
1.39
2.82
0.012
0.0195
0.006
0.004
0.033





INV. EX.


U
0.160
1.24
2.58
0.011

0.0204

0.004
0.004
0.042





COMP. EX.


V
0.157
1.38
2.80
0.009
0.0012
0.004
0.005
0.924





INV. EX.


W
0.166
1.36
2.47
0.011
0.0014
0.002
0.004

1.049






COMP. EX.


X
0.187
1.25
2.61
0.010
0.0006
 0.0090
0.005
0.013





INV. EX.


Y
0.186
1.05
2.65
0.010
0.0014
0.0110
0.005
0.059





COMP. EX.


Z
0.167
1.34
2.87
0.008
0.0011
0.006
 0.0090
0.026





INV. EX.


AA
0.180
1.33
2.65
0.015
0.0009
0.007
0.0110
0.026





COMP. EX.


AB
0.176
1.24
2.77
0.007
0.0012
0.004
0.007
0.047





INV. EX.


AC
0.188
1.22
2.68
0.006
0.0011
0.005
0.007
0.042
0.003




INV. EX.


AD
0.152
1.14
2.71
0.010
0.0014
0.002
0.003
0.054
0.196




INV. EX.


AE
0.156
1.18
2.46
0.011
0.0006
0.007
0.004
0.035

0.204





COMP. EX.


AF
0.183
1.14
2.47
0.007
0.0015
0.005
0.004
0.048

0.0003



INV. EX.


AG
0.154
1.18
2.77
0.009
0.0011
0.006
0.004
0.027

0.0075



INV. EX.


AH
0.183
1.34
2.86
0.009
0.0007
0.003
0.004
0.029


0.0106




COMP. EX.


Al
0.178
1.27
2.89
0.009
0.0010
0.002
0.006
0.020


0.001


INV. EX.


AJ
0.164
1.16
2.51
0.011
0.0005
0.002
0.002
0.035


0.183


INV. EX.


AK
0.167
1.08
2.55
0.014
0.0006
0.004
0.004
0.055



0.204



COMP. EX.


AL
0.154
1.04
2.67
0.005
0.0015
0.002
0.003
0.035



0.02

INV. EX.


AM
0.176
1.20
2.47
0.005
0.0011
0.004
0.005
0.053



0.95

INV. EX.





Underlines indicate being outside the range of the present invention.















TABLE 2








Chemical composition (mass %)






















Steels
C
Si
Mn
P
S
N
O
Al
Ti
B
Nb
Cu
Others

























AN
0.178
1.22
2.78
|0.009
0.0011
0.004
0.007
0.035




1.05


COMP. EX.


AO
0.177
1.03
2.46
0.014
0.0012
0.006
0.002
0.035




V: 0.126
INV. EX.


AP
0.166
1.06
2.50
0.006
0.0014
0.002
0.003
0.045




Ta: 0.01
INV. EX.


AQ
0.161
1.14
2.62
0.005
0.0012
0.001
0.006
0.037




W: 0.04
INV. EX.


AR
0.163
1.15
2.88
0.009
0.0013
0.006
0.007
0.025




Cr: 0.71
INV. EX.


AS
0.155
1.08
2.87
0.012
0.0007
0.003
0.002
0.023




Mo: 0.07
INV. EX.


AT
0.173
1.24
2.53
0.013
0.0013
0.003
0.002
0.036




Co: 0.008
INV. EX.


AU
0.178
1.15
2.86
0.007
0.0011
0.004
0.005
0.056




Ni: 0.18
INV. EX.


AV
0.167
1.01
2.47
0.005
0.0014
0.004
|0.001
0.051




Sn: 0.131
INV. EX.


AV
0.173
1.06
2.42
0.006
0.0011
0.003
0.004
0.037




Sb: 0.026
INV. EX.


AX
0.189
1.01
2.73
0.012
0.0008
0.005
0.007
0.054




Ca: 0.0073
INV. EX.


AY
0.184
1.15
2.82
0.007
0.0006
0.003
0.006
0.022




Mg: 0.0014
INV. EX.


AZ
0.184
1.04
2.52
0.012
0.0014
0.002
0.006
0.011




Zr: 0.072
INV. EX.


BA
0.158
1.39
2.55
0.014
0.0013
0.006
0.007
0.027




Te: 0.024
INV. EX.


BB
0.190
1.36
2.89
0.013
0.0011
0.006
0.005
0.053




Hf: 0.10
INV. EX.


BC
0.164
1.12
2.74
0.008
0.0011
0.003
0.003
0.039




REM: 0.0097
INV. EX.


BD
0.183
1.06
2.80
0.011
0.0012
0.002
0.005
0.011




Bi: 0.153
INV. EX.


BE
0.158
1.33
2.65
0.007
0.0015
0.006
0.004
0.033




Zn: 0.074
INV. EX.


BF
0.176
1.26
2.49
0.010
0.0007
0.004
0.006
0.014




Pb: 0.076
INV. EX.


BG
0.159
1.08
2.68
0.012
0.0008
0.001
0.004
0.052




As: 0.096
INV. EX.


BH
0.178
1.15
2.53
0.011
0.0008
0.004
0.002
0.019




Ge: 0.022
INV. EX.


BI
0.178
1.38
2.75
0.006
0.0012
0.001
0.001
0.043




Sr: 0.012
INV. EX.


BJ
0.167
1.02
2.41
0.014
0.0015
0.006
0.001
0.036




Cs: 0.047
INV. EX.


BK
0.156
1.18
2.55
0.014
0.0010
0.003
0.006
0.049





INV. EX.


BL
0.150
1.02
2.88
0.014
0.0007
0.006
0.005
0.040





INV. EX.


BM
0.187
1.21
2.67
0.015
0.0013
0.006
0.006
0.014





INV. EX.


BN
0.161
1.32
2.57
0.014
0.0009
0.006
0.006
0.047





INV. EX.


BO
0.175
1.02
2.73
0.011
0.0008
0.001
0.005
0.047





INV. EX.





Underlines indicate being outside the range of the present invention.






















TABLE 3












Average
Average
Count of








Count of
cooling
cooling
bending and








bending and
rate in
rate in
unbending in








unbending
temperature
temperature
temperature






Annealing
Annealing
during
range of
range of
range of






temp. Ta
time
annealing
700-600° C.
499° C.-Ms
499° C.-Ms
Ms
(Ms-80)


Nos.
Steels
(° C.)
(s)
(times)
(° C./s)
(° C./s)
(times)
(° C.)
(° C.)





 1
A
837
142
10
80
13
 3
350
270


 2
B
840
129
10
68
13
 3
347
267


 3
B
740
 81
10
63
15
 3
348
268


 4
B

697

 74
10
60
11
 3
349
269


 5
B
890
180
10
51
15
 3
347
267


 6
B

901

132
10
74
12
 3
346
266


 7
B
828
 23
10
59
12
 3
347
267


 8
B
842
6
10
55
10
 3
347
267


 9
B
808
809
10
53
11
 3
348
268


10
B
845

1020

10
63
13
 3
347
267


11
B
829
131
 1
65
13
 3
347
267


12
B
827
186
0
60
13
 3
347
267


13
B
847
110
15
59
10
 3
347
267


14
B
842
 50
15
64
12
 3
347
267


15
B
830
131
 3
22
11
 3
347
267


16
B
839
176
 3

12

12
 3
347
267


17
B
849
 99
 3
73
11
 3
347
267


18
B
808
 89
 3
67
12
 3
348
268


19
B
803
100
 3
73
19
 3
348
268


20
B
812
 74
 3
67

28

 3
347
267


21
B
802
133
 3
75
14
 3
348
268


22
B
842
161
 3
58
12
 3
347
267


23
B
811
 82
 3
73
12
 1
348
268


24
B
824
105
 3
77
12
0
347
267


25
B
841
 73
 3
63
12
15
347
267


26
B
827
165
 3
54
15
15
347
267


27
B
803
173
 3
51
15
 3
348
268


28
B
842
 98
 3
79
15
 3
347
267


29
B
818
187
 3
75
14
 3
347
267


30
B
828
 71
 3
61
12
 3
347
267


31
B
833
193
 3
75
11
 3
347
267


32
B
825
129
 3
55
14
 3
347
267


33
B
819
 65
 3
67
14
 3
347
267


34
B
817
125
10
64
12
 3
347
267


35
B
841
123
10
58
12
 3
347
267


36
B
803
 63
10
69
12
 3
348
268


37
B
823
 66
10
69
14
 3
347
267


38
B
847
166
10
60
13
 3
347
267


39
B
806
 72
10
64
15
 3
348
268


40
B
825
120
10
66
13
 3
347
267


41
B
844
170
10
74
12
 3
347
267


42
B
810
124
10
75
13
 3
348
268


43
B
846
111
10
68
11
10
347
267


44
B
821
167
 3
73
13
10
347
267


45
B
830
 71
 3
71
13
10
347
267


46
B
831
196
 3
77
14
10
347
267


47
B
827
 80
 3
69
14
10
347
267


48
B
830
158
 3
62
14
10
347
267


49
C
841
123
 3
58
11
10
352
272


50
D
826
188
 3
59
11
10
342
262


51
E
809
134
 3
56
12
 3
346
266


52
F
802
157
 3
77
12
 3
411
331


53
G
849
143
 3
55
13
 3
418
338









Average











cooling










Cooling
rate in
Tension in









stop
temperature
temperature









temp.
range of
range of
Tempering
Tempering







Tb
Ms-Tb
Ms-Tb
temp.
time






Nos.
(° C.)
(° C./s)
(MPa)
(° C.)
(s)
Type*







 1
232
16
13
333
223
CR
INV. EX.




 2
202
14
 8
258
131
CR
INV. EX.




 3
231
16
10
327
119
CR
INV. EX.




 4
222
19
 9
290
144
CR
COMP. EX.




 5
202
19
16
330
104
CR
INV. EX.




 6
226
19
 9
348
228
CR
COMP. EX.




 7
198
14
10
282
119
CR
INV. EX.




 8
206
18
13
261
224
CR
COMP. EX.




 9
200
14
 8
284
188
CR
INV. EX.




10
206
17
18
268
297
CR
COMP. EX.




11
205
13
13
308
179
CR
INV. EX.




12
218
13
15
264
129
CR
COMP. EX.




13
200
11
17
326
235
CR
INV. EX.




14
205
16
12
294
184
CR
INV. EX.




15
202
14
 9
310
278
CR
INV. EX.




16
233
18
11
274
253
CR
COMP. EX.




17
216
11
15
257
132
CR
INV. EX.




18
205
17
 8
326
262
CR
INV. EX.




19
215
17
13
326
156
CR
INV. EX




20
230
17
12
302
295
CR
COMP. EX.




21
198
103 
18
279
219
CR
INV. EX.




22
219
14
13
219
246
CR
INV. EX.




23
234
16
12
251
278
CR
INV. EX.




24
198
14
10
275
282
CR
COMP. EX.




25
201
17
15
338
238
CR
INV. EX.




26
211
13
17
313
101
CR
INV. EX.




27
104
14
10
312
265
CR
INV. EX.




28
95
17
13
313
280
CR
COMP. EX.




29
267
16
15
284
189
CR
INV. EX.




30

272

11
10
309
259
CR
COMP. EX.




31
222
13
12
285
278
CR
INV. EX.




32
232
13
15
296
262
CR
INV. EX




33
220
149 
17
311
106
CR
INV. EX.




34
216

155

17
344
274
CR
COMP. EX.




35
222
15
 5
293
258
CR
INV. EX.




36
201
14
4
338
114
CR
COMP. EX.




37
216
18
99
276
184
CR
INV. EX.




38
219
16

104

347
137
CR
COMP. EX.




39
223
14
14
223
242
CR
INV. EX.




40
206
13
15
206
106
CR
INV. EX.




41
226
19
13
420
151
CR
INV. EX




42
211
18
17
448
273
CR
INV. EX.




43
235
19
 8
282
 23
CR
INV. EX.




44
237
17
11
303
3
CR
COMP. EX.




45
203
14
15
347
964
CR
INV. EX.




46
224
16
 8
327
824
CR
INV. EX




47
210
15
 8
320
266
CR
INV. EX.




48
200
95
12
285
101
CR
INV. EX.




49
202
105 
11
288
214
CR
INV. EX.




50
201
16
12
321
103
CR
INV. EX.




51
210
11
12
287
281
CR
INV. EX




52
269
10
 9
345
270
CR
INV. EX.




53
279
14
14
349
122
CR
COMP. EX.





Underlines indicate being outside the range of the present invention.


(*)CR: cold rolled steel sheet (no coating), GI: hot-dip galvanized steel sheet (no alloying of zinc coating), GA: galvannealed steel sheet, EG: electrogalvanized steel sheet






















TABLE 4












Average
Average
Count of








Count of
cooling
cooling
bending and








bending and
rate in
rate in
unbending in








unbending
temperature
temperature
temperature






Annealing
Annealing
during
range of
range of
range of






temp. Ta
time
annealing
700-600° C.
499° C.-Ms
499° C.-Ms
Ms
(Ms-80)


Nos.
Steels
(° C.)
(s)
(times)
(° C./s)
(° C./s)
(times)
(° C.)
(° C.)





54
H
816
172
 3
56
13
 3
216
136


55
I
839
183
 3
79
13
 3
183
103


56
J
840
157
 3
58
13
 3
337
257


57
K
821
141
 3
59
11
 3
349
269


58
L
825
147
 3
78
15
 3
343
263


59
M
824
157
10
67
12
 3
344
264


60
N
846
112
10
75
12
 3
398
318


61
O
832
167
10
68
14
 3
399
319


62
P
824
 61
10
66
11
 3
281
201


63
Q
807
158
10
61
13
 3
268
188


64
R
805
110
10
71
13
 3
345
265


65
S
808
123
 3
63
11
 3
348
268


66
T
830
100
 3
58
14
 3
336
256


67
U
826
194
 3
59
11
 3
354
274


68
V
805
174
 3
70
11
 3
349
269


69
W
815
161
 3
52
15
 3
355
275


70
X
824
121
 3
61
13
10
341
261


71
Y
844
 54
 3
68
11
10
340
260


72
Z
818
 76
 3
50
14
10
342
262


73
AA
806
181
 3
50
11
10
343
263


74
AB
812
140
 3
80
12
10
341
261


75
AC
811
 86
 3
62
14
10
338
258


76
AD
842
 97
 3
57
14
10
354
274


77
AE
804
 64
 3
76
11
10
360
280


78
AF
801
168
 3
72
14
 3
347
267


79
AG
822
 76
 3
78
13
 3
352
272


80
AH
837
109
10
70
12
 3
335
255


81
AI
840
100
10
56
12
 3
336
256


82
AJ
832
 76
10
64
14
 3
355
275


83
AK
810
186
10
63
13
 3
352
272


84
AL
807
 95
10
65
13
 3
355
275


85
AM
848
136
10
68
13
 3
350
270


86
AN
834
181
10
70
14
 3
340
260


87
AO
749
 90
10
55
11
 3
351
271


88
AP
876
150
10
74
10
 3
353
273


89
AQ
832
 27
10
64
11
 3
353
273


90
AR
828
846
10
73
12
 3
335
255


91
AS
828
141
 1
56
11
 3
347
267


92
AT
849
157
15
77
15
 3
349
269


93
AU
803
 90
 3
25
13
 3
334
254


94
AV
849
197
 3
65
15
 3
354
274


95
AW
846
152
10
55
18
 3
353
273


96
AX
826
 62
10
60
11
 3
336
256


97
AY
838
 99
10
50
14
 1
336
256


98
AZ
840
 97
10
60
14
15
345
265


99
BA
824
 60
 3
72
14
 3
356
276


100
BB
848
162
 3
55
15
 3
330
250


101
BC
820
165
10
64
12
 3
348
268


102
BD
829
131
10
66
13
 3
337
257


103
BE
807
 70
 3
72
13
 3
353
273


104
BF
840
 65
 3
76
11
 3
349
269


105
BG
805
139
10
71
12
 3
352
272


106
BH
846
142
10
63
12
 3
347
267


107
BI
837
 63
10
76
13
 3
341
261


108
BJ
822
109
10
53
13
 3
356
276


109
BK
822
 59
10
53
11
12
357
277


110
BL
838
 70
 5
50
13
12
350
270


111
BM
830
 57
 5
58
11
 3
339
259


112
BN
802
 57
12
62
13
 3
355
275


113
BC
847
198
12
54
12
 3
342
262









Average











cooling










Cooling
rate in
Tension in









stop
temperature
temperature









temp.
range of
range of
Tempering
Tempering







Tb
Ms-Tb
Ms-Tb
temp.
time






Nos.
(° C.)
(° C./s)
(MPa)
(° C.)
(s)
Type*







54
110
12
14
318
158
CR
INV. EX.




55
101
20
17
299
117
CR
COMP. EX.




56
198
19
10
276
115
CR
INV. EX.




57
230
17
13
281
282
CR
COMP. EX.




58
197
16
16
347
188
CR
INV. EX.




59
226
13
17
275
286
GA
COMP. EX.




60
265
13
15
334
181
GA
INV. EX.




61
259
11
16
321
163
GA
COMP. EX.




62
150
11
12
278
234
GA
INV. EX.




63
123
17
11
259
102
GA
COMP. EX.




64
195
12
 9
346
271
CR
INV. EX.




65
207
18
 8
270
104
CR
COMP. EX.




66
199
16
14
260
218
GA
INV. EX.




67
231
14
14
314
197
GA
COMP. EX.




68
200
15
11
319
199
GI
INV. EX.




69
227
19
11
347
259
GA
COMP. EX.




70
195
12
14
331
109
GA
INV. EX.




71
229
11
14
311
161
GA
COMP. EX.




72
205
13
14
299
208
GA
INV. EX.




73
231
18
10
284
162
GI
COMP. EX.




74
225
19
15
335
114
GA
INV. EX.




75
199
12
12
292
190
GA
INV. EX.




76
226
19
18
270
129
GA
INV. EX.




77
247
17
 9
285
234
GA
COMP. EX.




78
230
15
15
313
235
GA
INV. EX.




79
214
11
 8
332
192
GI
INV. EX.




80
187
18
16
290
135
GA
COMP. EX.




81
212
19
16
275
273
GA
INV. EX.




82
222
16
 9
305
180
GA
INV. EX.




83
208
14
 9
263
114
GA
COMP. EX.




84
220
11
11
269
174
CR
INV. EX.




85
202
11
17
276
151
CR
INV. EX.




86
207
19
10
285
211
GA
COMP. EX.




87
215
13
12
318
104
GA
INV. EX.




88
218
15
17
321
181
GA
INV. EX.




89
212
18
18
298
191
GA
INV. EX.




90
204
15
12
282
290
GA
INV. EX.




91
219
18
15
262
224
GA
INV. EX.




92
203
12
15
348
183
GA
INV. EX.




93
209
13
15
292
107
CR
INV. EX.




94
242
11
11
338
232
CR
INV. EX.




95
206
18
 8
252
208
CR
INV. EX.




96
207
19
17
207
160
CR
INV. EX.




97
199
14
16
283
278
CR
INV. EX.




98
218
16
10
328
293
CR
INV. EX.




99
110
14
15
326
300
CR
INV. EX.




100
248
11
 8
344
277
CR
INV. EX.




101
210
13
11
257
201
CR
INV. EX.




102
208
137 
15
297
252
CR
INV. EX.




103
209
10
 6
308
231
CR
INV. EX.




104
214
16
100 
298
229
CR
INV. EX.




105
237
13
15
237
170
CR
INV. EX.




106
201
17
15
405
113
CR
INV. EX.




107
213
12
15
300
15
CR
INV. EX.




108
232
18
14
270
847
CR
INV. EX.




109
225
17
15
308
215
EG
INV. EX.




110
221
15
10
257
294
GI
INV. EX.




111
221
13
16
273
287
EG
INV. EX.




112
236
92
11
323
109
GI
INV. EX.




113
225
105 
 9
317
219
GA
INV. EX.





Underlines indicate being outside the range of the present invention.


(*)CR: cold rolled steel sheet (no coating), GI: hot-dip galvanized steel sheet (no alloying of zinc coating), GA: galvannealed steel sheet, EG: electrogalvanized steel sheet






(Microstructure Observation)

The amount of martensite, the amount of retained austenite, and the total amount of ferrite and bainitic ferrite were determined by the methods described hereinabove.


(Proportion of Packets Having the Largest Area in Prior Austenite Grains)

The average proportion of packets having the largest area in prior austenite grains was determined by the method described hereinabove.


(Tensile Test)

A JIS No. 5 test specimen (gauge length: 50 mm, parallel section width: 25 mm) was sampled so that the longitudinal direction of the test specimen would be perpendicular to the rolling direction. A tensile test was performed in accordance with JIS Z 2241 under conditions where the crosshead speed was 1.67×10−1 mm/sec. TS and El were thus measured. In accordance with aspects of the present invention, 980 MPa or higher TS was determined to be acceptable, and 10% or more El was determined to be acceptable.


(Toughness)

Toughness was evaluated by Charpy test. A Charpy test specimen was a 2 mm deep V-notched test piece that was a stack of steel sheets fastened together with bolts to eliminate any gaps between the steel sheets. The number of steel sheets that were stacked was controlled so that the thickness of the stack as the test piece would be closer to 10 mm. When, for example, the sheet thickness was 1.2 mm, eight sheets were stacked to give a 9.6 mm thick test piece. The Charpy test specimen was evaluated as “excellent in toughness” when the stack had a strength of 40 J/cm2 or more. Conditions other than those described above conformed to JIS Z 2242:2018.


(Flatness in the Width Direction)

The cold rolled steel sheets obtained as described above were analyzed to measure the flatness in the width direction. The measurement is illustrated in FIG. 2. Specifically, a sheet with a length of 500 mm in the rolling direction (coil width×500 mm L×sheet thickness) was cut out from the coil and was placed on a surface plate in such a manner that the warp at the ends would face upward. The height on the steel sheet was measured with a contact displacement meter by continuously moving the stylus over the width. Based on the results, the steepness as an index of the flatness of the steel sheet shape was measured as illustrated in FIG. 2. The flatness was rated as “x” when the steepness was more than 0.02, as “o” when the steepness was more than 0.01 and 0.02 or less, and as “@” when the steepness was 0.01 or less. The steel sheet was evaluated as “excellent in the flatness in the width direction” when the steepness was 0.02 or less.


(Working Embrittlement Resistance)

The working embrittlement resistance was evaluated by Charpy test. A Charpy test specimen was a 2 mm deep V-notched test piece that was a stack of steel sheets fastened together with bolts to eliminate any gaps between the steel sheets. The number of steel sheets that were stacked was controlled so that the thickness of the stack as the test piece would be closer to 10 mm. When, for example, the sheet thickness was 1.2 mm, eight sheets were stacked to give a 9.6 mm thick test piece. The sheets for stacking into the Charpy test specimen were sampled so that the width direction would be the longitudinal direction. As an index of the working embrittlement resistance, the ratio vE0%/vE10% of the absorbed impact energy at room temperature of the as-produced (unworked) steel sheet to that of the steel sheet after 10% rolling was measured. The working embrittlement resistance was rated as “×” when vE0%/vE10% was less than 0.6, as “∘” when vE0%/VE10% was 0.6 or more and less than 0.7, and as “⊚” when vE0%/vE10% was 0.7 or more. The Charpy test specimen was evaluated as “excellent in working embrittlement resistance” when vE0%/vE10% was 0.6 or more. Conditions other than those described above conformed to JIS Z 2242:2018.


The results are described in Tables 5 to 7. As shown in Tables 5 to 7, INVENTIVE EXAMPLES achieved 980 MPa or higher TS, 10% or more El, and excellent toughness, flatness in the width direction, and working embrittlement resistance. In contrast, COMPARATIVE EXAMPLES were unsatisfactory in one or more of TS, El, toughness, flatness in the width direction, and working embrittlement resistance.




















TABLE 5









Total of
Average proportion












ferrite and
of packets having











Retained
bainitic
the largest area in


Absorbed
Flatness
Working





Martensite
austenite
ferrite
prior austenite
TS
EI
energy
in width
embrittlement



Nos.
Steels
(area %)
(vol %)
(area %)
grains (area %)
(MPa)
(%)
(J/cm2)
direction
resistance


























1
A
70
11
19
47
1283
19
51


INV. EX.


2
B
71
11
18
50
1277
20
50


INV. EX.


3
B
61
 8
31
49
1010
33
53


INV. EX.


4
B

53

 8
39
46
928
32
55


COMP. EX.


5
B
79
10
11
48
1394
11
45


INV. EX.


6
B
84
 9
7
59
1632
8
50


COMP. EX.


7
B
60
 8
32
60
1009
35
50


INV. EX.


8
B

49

11
40
48
897
33
51


COMP. EX.


9
B
77
10
13
47
1238
11
49


INV. EX.


10
B
82
10
8
52
1113
8
49


COMP. EX.


11
B
75
 8
17
69
1158
20
49


INV. EX.


12
B
77
 9
14

80

1232
16
51

X


X

COMP. EX.


13
B
71
11
18
48
1197
21
41


INV. EX.


14
B
71
10
19
58
1118
18
41


INV. EX.


15
B
70
11
19
68
1357
14
50


INV. EX.


16
B
73
 9
18

88

1274
17
54

X


X

COMP. EX.


17
B
71
11
18
53
1271
16
48


INV. EX.


18
B
74
10
16
58
1314
19
45


INV. EX.


19
B
79
10
11
50
1355
11
46


INV. EX.


20
B
82
 9
9
47
1467
9
47


COMP. EX.


21
B
68
12
20
56
1267
19
49


INV. EX.


22
B
75
10
15
58
1198
15
53


INV. EX.


23
B
73
11
16
66
1157
21
48


INV. EX.


24
B
73
 9
18

92

1357
15
46

X


X

COMP. EX.


25
B
70
11
19
50
1235
20
41


INV. EX.


26
B
69
11
20
60
1109
18
42


INV. EX.


27
B
78
 4
18
52
1236
10
42


INV. EX.


28
B
80
2
18
59
1591
8

33



COMP. EX.


29
B
71
13
16
54
1035
24
63


INV. EX.


30
B
66

16

18
49
1033
28
62


X

COMP. EX.


31
B
72
10
18
45
1278
17
51


INV. EX.


32
B
72
10
18
47
1267
15
47


INV. EX.


33
B
71
10
19
67
1308
18
54


INV. EX.


34
B
73
12
15

81

1232
19
46

X


X

COMP. EX.


35
B
70
12
18
68
1227
17
45


INV. EX.


36
B
71
10
19

89

1272
18
45

X


X

COMP. EX.





Underlines indicate being outside the range of the present invention.
























TABLE 6









Total of
Average proportion












ferrite and
of packets having











Retained
bainitic
the largest area in


Absorbed
Flatness
Working





Martensite
austenite
ferrite
prior austenite
TS
EI
energy
in width
embrittlement



Nos.
Steels
(area %)
(vol %)
(area %)
grains (area %)
(MPa)
(%)
(J/cm2)
direction
resistance







37
B
64
 9
27
55
 999
25
42


INV. EX.


38
B

54

10
36
59
884
30
40


COMP. EX.


39
B
70
10
20
57
1237
18
54


INV. EX.


40
B
71
10
19
55
1234
15
46


INV. EX.


41
B
72
 9
19
48
1012
25
52


INV. EX.


42
B
75
10
15
51
 985
23
46


INV. EX.


43
B
83
 3
14
58
1307
10
40


INV. EX.


44
B
80
2
18
54
1433
9

30



COMP. EX.


45
B
71
12
17
46
1006
23
50


INV. EX.


46
B
73
10
17
56
1017
27
52


INV. EX.


47
B
74
11
15
59
1039
20
55


INV. EX.


48
B
73
10
17
47
1317
19
55


INV. EX.


49
C
73
 9
18
49
1114
18
52


INV. EX.


50
D
76
 8
16
53
1284
17
52


INV. EX.


51
E
77
 9
14
46
1332
17
47


INV. EX.


52
F
60
 8
32
52
 989
30
45


INV. EX.


53
G

48

12
40
54
920
35
55


COMP. EX.


54
H
72
10
18
54
1604
11
42


INV. EX.


55
I
77
 9
14
48
1766
11

26



X

COMP. EX.


56
J
69
11
20
55
1014
25
45


INV. EX.


57
K
72
11
17
58
898
25
54


COMP. EX.


58
L
69
13
18
51
1342
17
58


INV. EX.


59
M
70

16

14
56
1095
27
60


X

COMP. EX.


60
N
61
 9
30
59
1017
31
48


INV. EX.


61
O

52

12
36
56
899
30
48


COMP. EX.


62
P
74
11
15
48
1216
21
41


INV. EX.


63
Q
73
12
15
54
1535
15

33



X

COMP. EX.


64
R
74
10
16
48
1189
19
41


INV. EX.


65
S
73
11
16
54
1175
17

28



X

COMP. EX.


66
T
73
10
17
48
1372
17
42


INV. EX.


67
U
72
10
18
60
1117
18

28



X

COMP. EX.


68
V
70
12
18
51
1299
17
41


INV. EX.


69
W
71
11
18
48
1144
17

30



X

COMP. EX.


70
X
74
 8
18
54
1362
15
40


INV. EX.


71
Y
76
 9
15
52
1349
15

31



X

COMP. EX.





Underlines indicate being outside the range of the present invention.
























TABLE 7









Total of
Average proportion












ferrite and
of packets having











Retained
bainitic
the largest area in


Absorbed
Flatness
Working





Martensite
austenite
ferrite
prior austenite
TS
EI
energy
in width
embrittlement



Nos.
Steels
(area %)
(vol %)
(area %)
grains (area %)
(MPa)
(%)
(J/cm2)
direction
resistance


























72
Z
75
10
15
47
1277
19
42


INV. EX.


73
AA
73
 9
18
48
1387
15

26



X

COMP. EX.


74
AB
72
10
18
57
1415
19
46


INV. EX.


75
AC
75
10
15
57
 994
23
52


INV. EX.


76
AD
73
10
17
52
1169
20
42


INV. EX.


77
AE
77
 9
14
54
1676
12

27



X

COMP. EX.


78
AF
77
 9
14
59
1010
25
47


INV. EX.


79
AG
73
 9
18
57
1151
22
43


INV. EX.


80
AH
72
11
17
51
1630
15

29



X

COMP. EX.


81
AI
75
 9
16
56
1014
18
46


INV. EX.


82
AJ
74
11
15
46
1271
17
42


INV. EX.


83
AK
74
11
15
46
1554
13

26



X

COMP. EX.


84
AL
71
 9
20
48
1006
23
49


INV. EX.


85
AM
71
10
19
57
1350
19
42


INV. EX.


86
AN
72
 9
19
47
1515
14

28



X

COMP. EX.


87
AO
60
 8
32
48
1015
30
47


INV. EX.


88
AP
76
11
13
46
1393
11
51


INV. EX.


89
AQ
61
 9
30
46
1005
33
49


INV. EX.


90
AR
76
12
12
56
1417
12
55


INV. EX.


91
AS
75
 8
17
59
1104
24
47


INV. EX.


92
AT
78
 8
14
49
1225
20
41


INV. EX.


93
AU
69
12
19
69
1304
18
55


INV. EX.


94
AV
70
11
19
50
1349
17
49


INV. EX.


95
AW
61
 9
30
59
 993
34
51


INV. EX.


96
AX
74
 8
18
48
1195
19
50


INV. EX.


97
AY
78
 8
14
64
1121
21
47


INV. EX.


98
AZ
72
12
16
52
1129
20
50


INV. EX.


99
BA
77
 3
20
51
1354
10
45


INV. EX.


100
BB
68
13
19
54
1198
20
54


INV. EX.


101
BC
76
 9
15
50
1367
18
52


INV. EX.


102
BD
73
11
16
62
1183
18
53


INV. EX.


103
BE
75
 8
17
67
1116
19
53


INV. EX.


104
BF
70
11
19
59
1357
17
42


INV. EX.


105
BG
75
 9
16
46
1187
15
45


INV. EX.


106
BH
72
 9
19
56
1017
27
52


INV. EX.


107
BI
81
 4
15
50
1468
10
42


INV. EX.


108
BJ
75
 9
16
58
1007
23
53


INV. EX.


109
BK
73
11
16
51
1063
25
54


INV. EX.


110
BL
71
11
18
53
1090
21
53


INV. EX.


111
BM
70
10
20
58
1320
18
49


INV. EX.


112
BN
69
12
19
52
1122
21
49


INV. EX.


113
BO
70
10
20
46
1319
16
48


INV. EX.





Underlines indicate being outside the range of the present invention.





Claims
  • 1. A high strength steel sheet having a chemical composition comprising, in mass %, C: 0.030% or more and 0.500% or less,Si: 0.50% or more and 2.50% or less,Mn: 1.00% or more and 5.00% or less,P: 0.100% or less,S: 0.0200% or less,Al: 1.000% or less,N: 0.0100% or less, andO: 0.0100% or less,a balance being Fe and incidental impurities,the high strength steel sheet being such that in a region at ¼ sheet thickness,an area fraction of martensite is 60% or more,a volume fraction of retained austenite is 3% or more and 15% or less,an area fraction of a total of ferrite and bainitic ferrite is more than 10%, andan average of proportions of packets having the largest area in prior austenite grains is 70% by area or less of the prior austenite grain.
  • 2. The high strength steel sheet according to claim 1, wherein the chemical composition further comprises at least one element selected from, in mass %, 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,Co: 0.010% or less, Ni: 1.00% 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 high strength steel sheet according to claim 1, which has a coated layer on a surface of the steel sheet.
  • 4. The high strength steel sheet according to claim 2, which has a coated layer on a surface of the steel sheet.
  • 5. A method for manufacturing the high strength steel sheet according to claim 1, the method comprising: providing a cold rolled steel sheet produced by subjecting a steel having the chemical composition to hot rolling, pickling, and cold rolling;annealing the steel sheet by heating at an annealing temperature Ta of 700° C. or above and 900° C. or below for a holding time at the annealing temperature Ta of 10 seconds or more and 1000 seconds or less;bending and unbending the steel sheet 1 to 15 times in total with a roll having a radius of 800 mm or less during the annealing;cooling the steel sheet at an average cooling rate of 20° C./s or more in a temperature range from 700° C. to 600° C. and at an average cooling rate of less than 20° C./s in a temperature range from 499° C. to Ms;bending and unbending the steel sheet in the temperature range from 499° C. to Ms, 1 to 15 times in total with a roll having a radius of 800 mm or less;cooling the steel sheet at an average cooling rate of 150° C./s or less in a temperature range from Ms to a cooling stop temperature Tb;applying a tension to the steel sheet in the temperature range from Ms to the cooling stop temperature Tb while controlling the tension to 5 MPa or more and 100 MPa or less,the cooling stop temperature Tb being 100° C. or above and (Ms−80° C.) or below where Ms is a martensite start temperature (° C.) defined by formula (1); andtempering the steel sheet at a tempering temperature of Tb or above and 450° C. or below for a holding time at the tempering temperature of 10 seconds or more and 1000 seconds or less,
  • 6. A method for manufacturing the high strength steel sheet according to claim 2, the method comprising: providing a cold rolled steel sheet produced by subjecting a steel having the chemical composition to hot rolling, pickling, and cold rolling;annealing the steel sheet by heating at an annealing temperature Ta of 700° C. or above and 900° C. or below for a holding time at the annealing temperature Ta of 10 seconds or more and 1000 seconds or less;bending and unbending the steel sheet 1 to 15 times in total with a roll having a radius of 800 mm or less during the annealing;cooling the steel sheet at an average cooling rate of 20° C./s or more in a temperature range from 700° C. to 600° C. and at an average cooling rate of less than 20° C./s in a temperature range from 499° C. to Ms;bending and unbending the steel sheet in the temperature range from 499° C. to Ms, 1 to 15 times in total with a roll having a radius of 800 mm or less;cooling the steel sheet at an average cooling rate of 150° C./s or less in a temperature range from Ms to a cooling stop temperature Tb;applying a tension to the steel sheet in the temperature range from Ms to the cooling stop temperature Tb while controlling the tension to 5 MPa or more and 100 MPa or less,the cooling stop temperature Tb being 100° C. or above and (Ms−80° C.) or below where Ms is a martensite start temperature (° C.) defined by formula (1); andtempering the steel sheet at a tempering temperature of Tb or above and 450° C. or below for a holding time at the tempering temperature of 10 seconds or more and 1000 seconds or less,
  • 7. The method for manufacturing the high strength steel sheet according to claim 5, further comprising performing a coating treatment.
  • 8. The method for manufacturing the high strength steel sheet according to claim 6, further comprising performing a coating treatment.
Priority Claims (1)
Number Date Country Kind
2022-049759 Mar 2022 JP national
CROSS REFERENCE TO RELATED APPLICATIONS

This is the U.S. National Phase application of PCT/JP2023/002917, filed Jan. 30, 2023 which claims priority to Japanese Patent Application No. 2022-049759, filed Mar. 25, 2022, the disclosures of these applications being incorporated herein by reference in their entireties for all purposes.

PCT Information
Filing Document Filing Date Country Kind
PCT/JP2023/002917 1/30/2023 WO