Patent Application
20160237520
The present invention relates to a high-strength steel sheet having a tensile strength of 590 MPa or more and having excellent formability and low-temperature toughness and a method for producing the same.
In the field of automotive vehicles, it is an urgent need to address global environmental problems such as regulations on CO2 emission. On the other hand, in terms of ensuring passenger safety, collision safety standards of automotive vehicles have been reinforced and a structure design capable of sufficiently ensuring safety in a boarding space is in progress. To simultaneously achieve these requests, it is effective to use a high-strength steel sheet having a tensile strength of 590 MPa or more as a structure member of an automotive vehicle and reduce the weight of a vehicle body by further thinning this high-strength steel sheet. However, since formability is deteriorated if the strength of a steel sheet is increased, an improvement of formability is an unavoidable problem in applying the above high-strength steel sheet to an automotive member.
DP (Dual Phase) steel sheets whose metal structure is composed of ferrite and martensite and TRIP (Transformation Induced Plasticity) steel sheets utilizing transformation induced plasticity of retained austenite (hereinafter, referred to also as “retained γ”) are known as steel sheets having both strength and formability.
Particularly, in order to improve the strength and elongation of TRIP steel sheets, it is known to be effective that the metal structure contains retained γ.
For example, it is disclosed in patent literature 1 that the strength and formability, particularly elongation of a TRIP steel sheet can be improved by making a metal structure of a steel sheet a composite structure in which martensite and retained γ are intermingled in ferrite.
A technology for improving a balance of tensile strength (TE) and elongation (EL), specifically the press moldability of a TRIP steel sheet by improving TS×EL by making a metal structure of a steel sheet a structure containing ferrite, retained γ, bainite and/martensite is disclosed in patent literature 2. Particularly, retained γ is disclosed to have an action of improving the elongation of the steel sheet.
Although a high-strength steel sheet is desired to improve low-temperature toughness for collision safety improvement at low temperatures in addition to the above properties, TRIP steel sheets are known to be inferior in low-temperature toughness. Low-temperature toughness is not considered at all also in the above patent literature 1 and 2.
To produce a steel material having a tensile strength exceeding 780 MPa and having excellent low-temperature toughness, the refining of tempered martensite and low-temperature region generated bainite is thought to be effective. To refine tempered martensite and low-temperature region generated bainite, the refining of austenite before transformation is necessary. It is known that austenite can be refined, for example, by applying controlled rolling or rolling in an austenite recrystallization region.
For example, a steel material whose structure is refined by applying finish rolling at 780° C. or lower, which is a non-crystallization region of austenite, and which has excellent low-temperature toughness is disclosed in patent literature 3.
Patent literature 1: Publication of Japanese Patent No. 3527092
Patent literature 2: Publication of Japanese Patent No. 5076434
Patent literature 3: Japanese Unexamined Patent Publication No. H05-240355
In recent years, requests for the formability of steel sheets have become more and more strict. For example, steel sheets used for pillars, members and the like are required to be stretch-formed and drawn under stricter conditions. Thus, TRIP steel sheets are required to improve local deformability such as stretch flange formability and bendability without deteriorating strength and elongation. However, since retained γ transforms into very hard martensite during processing in TRIP steel sheets proposed thus far, there has been a problem of being inferior in local deformability such as stretch flange formability and bendability.
Further, since TRIP steel sheets tend to become poorer in low-temperature toughness with a strength increase, brittle fracture under a low temperature environment has become problematic.
The present invention was developed in view of the aforementioned situation and aims to provide a high-strength steel sheet having a tensile strength of 590 MPa or more, having excellent formability, particularly elongation and local deformability and having excellent low-temperature toughness and a method for producing the same.
The present invention capable of solving the above problem is directed to a steel sheet consisting of, in mass %, C: 0.10 to 0.5%, Si: 1.0 to 3%, Mn: 1.5 to 3.0%, Al: 0.005 to 1.0%, P: more than 0% and not more than 0.1%, S: more than 0% and not more than 0.05%, with the balance being iron and inevitable impurities, a metal structure of the steel sheet containing polygonal ferrite, bainite, tempered martensite and retained austenite, wherein:
(1) when the metal structure is observed by a scanning electron microscope,
(1a) an area percent a of the polygonal ferrite to the entire metal structure is higher than 50%;
(1b) the bainite is composed of a composite structure of high-temperature region generated bainite in which an average interval of distances between center positions of adjacent retained austenite grains, of adjacent carbide grains and of adjacent retained austenite grains and carbide grains is 1 μm or more and low-temperature region generated bainite in which an average interval of distances between center positions of adjacent retained austenite grains, of adjacent carbide grains and of adjacent retained austenite grains and carbide grains is less than 1 μm,
wherein an area percent b of the high-temperature region generated bainite to the entire metal structure is 5 to 40%, and
a total area percent c of the low-temperature region generated bainite and the tempered martensite to the entire metal structure is 5 to 40%;
(2) a volume percent of the retained austenite measured by a saturation magnetization method to the entire metal structure is 5% or higher,
(3) when an area enclosed by a boundary in which a crystal orientation difference measured by electron backscatter diffraction (EBSD) is 3° or larger is defined as a crystal grain, a distribution using each average IQ (Image Quality) based on the visibility of an EBSD pattern of the crystal grain analyzed for each crystal grain having a body centered cubic lattice (including a body centered tetragonal lattice) satisfies Equations (1) and (2) below:
(IQave−IQmin)/(IQmax−IQmin)≧0.40 (1)
(σIQ)/(IQmax−IQmin)≦0.25 (2)
(wherein IQave denotes an average value of average IQ total data of each crystal grain,
IQmin denotes a minimum value of average IQ total data of each crystal grain,
IQmax denotes a maximum value of average IQ total data of each crystal grain, and
σIQ denotes a standard deviation of the average IQ total data of each crystal grain).
In the present invention, it is also a preferred embodiment that, if MA mixed phases in which quenched martensite and the retained austenite are compounded are present when the metal structure is observed by an optical microscope, a number ratio of the MA mixed phases having a circle-equivalent diameter d larger than 7 μm to the total number of the MA mixed phases is 0% or more and below 15%.
Further, it is also a preferred embodiment that an average circle-equivalent diameter D of the polygonal ferrite grains is larger than 0 μm and not larger than 10 μm.
Further, the steel sheet of the present invention preferably contains at least one of the following (a) to (e):
(a) one or more elements selected from a group consisting of Cr: more than 0% and not more than 1% and Mo: more than 0% and not more than 1%,
(b) one or more elements selected from a group consisting of Ti: more than 0% and not more than 0.15%, Nb: more than 0% and not more than 0.15% and V: more than 0% and not more than 0.15%,
(c) one or more elements selected from a group consisting of Cu: more than 0% and not more than 1% and Ni: more than 0% and not more than 1%,
(d) B: more than 0% and not more than 0.005%,
(e) one or more elements selected from a group consisting of Ca: more than 0% and not more than 0.01%, Mg: more than 0% and not more than 0.01% and rare-earth elements: more than 0% and not more than 0.01%.
Further, it is also preferred that a surface of the steel sheet includes an electro-galvanized layer, a hot dip galvanized layer or an alloyed hot dip galvanized layer.
Further, the present invention also encompasses a method for producing a high-strength steel sheet, including:
heating a steel sheet satisfying the component composition to a temperature region of 800° C. or higher and an Ac3 point—10° C. or lower;
holding the steel sheet in this temperature region for 50 seconds or longer for soaking and then cooling the steel sheet at an average cooling rate of 20° C./s in a range of 600° C. or higher,
then cooling the steel sheet at an average cooling rate of 10° C./s or higher up to an arbitrary temperature T satisfying a range of 150° C. or higher and 400° C. or lower (an Ms point or lower if the Ms point expressed by Equation below is 400° C. or lower) and holding the steel sheet in a temperature region satisfying Equation (3) below for 10 to 200 seconds; and
subsequently heating the steel sheet to a temperature region satisfying Equation (4) below and cooling the steel sheet after holding the steel sheet in this temperature region for 50 seconds or longer:
150° C.≦T1(° C.)≦400° C. (3),
400° C.<T2(° C.)≦540° C. (4),
Ms point(° C.)=561−474×[C]/(1−Vf/100)−33×[Mn]−17×[Ni]−17×[Cr]−21×[Mo]
wherein Vf denotes a ferrite fraction measurement value in a sample replicating an annealing pattern from heating, soaking to cooling which is separately fabricated, and [ ] in Equation indicates a content (mass %) of each element and the content of the element not contained in the steel sheet is calculated as 0 mass %.
Furthermore, the producing method of the present invention includes cooling and, subsequently, electro-galvanizing, hot dip galvanizing or alloyed hot dip galvanizing applied after the steel sheet is held in the temperature region satisfying the Equation (4) or hot dip galvanizing or alloyed hot dip galvanizing applied in the temperature region satisfying the Equation (4).
According to the present invention, after polygonal ferrite is so generated that the area percent to the entire metal structure is higher than 50%, both bainite generated in a low temperature region and tempered martensite (hereinafter, written as “low-temperature region generated bainite and the like” in some cases) and bainite generated in a high temperature region (hereinafter, written as “high-temperature region generated bainite” in some cases) are generated and the IQ (Image Quality) distribution for each crystal grain having a body centered cubic (BCC) lattice crystal (including a body centered tetragonal (BCT) lattice crystal. The same applies to the following) measured by electron backscatter diffraction (EBSD) is controlled to satisfy Equations (1) and (2), whereby a high-strength steel sheet having excellent formability such as good elongation and local deformability and also having excellent low-temperature toughness can be realized even at a high strength region of 590 MPa or more. Further, according to the present invention, a method for producing the high-strength steel sheet can be provided.
The present inventors studied in depth to improve the formability, particularly elongation and local deformability, and low-temperature toughness of a high-strength steel sheet having a tensile strength of 590 MPa or more. As a result, they found the following and completed the present invention.
(1) A high-strength steel sheet having excellent formability can be provided by improving local deformability without deteriorating elongation if a metal structure of a steel sheet is made a mixed structure containing bainite, tempered martensite and retained γ, after being made to mainly contain polygonal ferrite, specifically such that an area percent to the entire metal structure is higher than 50% and, particularly the following two types of bainite are generated as bainite:
(1a) high-temperature region generated bainite in which an average interval of distances between center positions of adjacent retained γ gains, of adjacent carbide grains or of adjacent retained γ grains and carbide grains (hereinafter, these are collectively referred to as “retained γ grains and the like” in some cases) is 1 μm or more, and
(1b) low-temperature region generated bainite in which an average interval of distances between center positions of retained γ grains and the like is less than 1 μm.
(2) Specifically, the high-temperature region generated bainite contributes to an improvement of the elongation of the steel sheet and the low-temperature region generated bainite contributes to an improvement of the local deformability of the steel sheet.
(3) Further, a high-strength steel sheet having excellent low-temperature toughness can be provided by controlling such that an IQ distribution of each crystal grain having a body centered cubic lattice (including a body centered tetragonal lattice) satisfies relationships of Equation (1) [(IQave−IQmin)/(IQmax−IQmin)≧0.40] and Equation (2) [(σIQ)/(IQmax−IQmin)≦0.25].
(4) In order to generate a predetermined amount of polygonal ferrite, bainite, tempered martensite and retained austenite described above and realize a predetermined IQ distribution satisfying the above Equations (1) and (2), a steel sheet satisfying a predetermined component composition is heated to a two-phase temperature region of 800° C. or higher and an Ac3 point—10° C. or lower and soaked by being held in this temperature region for 50 seconds or longer, then cooled at an average cooling rate of 20° C./s in a range of 600° C. or higher, then cooled at an average cooling rate of 10° C./s up to an arbitrary temperature T satisfying 150° C. or higher and 400° C. or lower or an Ms point or lower if the Ms point is 400° C. or lower, held in a T1 temperature region satisfying Equation (3) [150° C.≦T1 (*C)≦400° C.] for 10 to 200 seconds, then heated to a T2 temperature region satisfying Equation (4) [400° C.<T2(° C.)≦540° C.] and held in this temperature region for 50 seconds or longer.
First, a metal structure characterizing the high-strength steel sheet according to the present invention is described.
<<Concerning Metal Structure>>
The metal structure of the high-strength steel sheet according to the present invention is a mixed structure of polygonal ferrite, bainite, tempered martensite and retained γ.
[Polygonal Ferrite]
The metal structure of the steel sheet of the present invention is mainly composed of polygonal ferrite. To be mainly composed of means that an area percent to the entire metal structure is higher than 50%. Polygonal ferrite is a structure which is softer than bainite and acts to improve formability by enhancing the elongation of the steel sheet. To exhibit such an action, the area percent of polygonal ferrite is set higher than 50%, preferably 55% or higher and more preferably 60% or higher to the entire metal structure. An upper limit of the area percent of polygonal ferrite is determined in consideration of a space factor of retained γ measured by a saturation magnetization method and, for example, 85%.
An average circle-equivalent diameter D of polygonal ferrite grains is preferably larger than 0 μm and not larger than 10 μm. The elongation of the steel sheet can be further improved by reducing the average circle-equivalent diameter D of the polygonal ferrite grains and finely dispersing the polygonal ferrite grains. This detailed mechanism is not elucidated, but uneven deformation hardly occurs since polygonal ferrite is evenly dispersed in the entire metal structure by refining polygonal ferrite. This is thought to contribute to a further improvement of the elongation. Specifically, when the metal structure of the steel sheet of the present invention is composed of a mixed structure of polygonal ferrite, bainite, tempered martensite and retained T, the individual structure varies in size if a grain diameter of polygonal ferrite increases. This is thought to cause uneven deformation and a local concentration of distortion, thereby making it difficult to improve formability, particularly an elongation improving action by the generation of polygonal ferrite. Thus, the average circle-equivalent diameter D of polygonal ferrite is preferably 10 μm or smaller, more preferably 8 μm or smaller, even more preferably 5 μm and particularly preferably 4 μm.
The above area percent and average circle-equivalent diameter D of polygonal ferrite can be measured through observation by a scanning electron microscope (SEM).
[Bainite and Tempered Martensite]
The steel sheet of the present invention is characterized in that bainite is composed of a composite structure of high-temperature region generated bainite and low-temperature region generated bainite having higher strength than high-temperature region generated bainite. High-temperature region generated bainite contributes to an improvement of the elongation of the steel sheet and low-temperature region generated bainite contributes to an improvement of the local deformability of the steel sheet. By containing these two kinds of bainite, local deformability can be improved and the formability of the steel sheet in general can be enhanced without deteriorating the elongation of the steel sheet. This is thought to be due to an increase of work hardening since uneven deformation is caused by compounding bainite structures having different strength levels.
The high-temperature region generated bainite is bainite generated in a relatively high temperature region out of a bainite generation region and a bainite structure generated mainly in a T2 temperature region higher than 400° C. and not higher than 540° C. The high-temperature region generated bainite is a structure in which an average interval of retained γ and the like is 1 μm or more when a nital corroded steel sheet cross-section is SEM observed.
On the other hand, the low-temperature region generated bainite is bainite generated in a relatively low temperature region and a bainite structure generated mainly in a T1 temperature region of 150° C. or higher and 400° C. or lower. The low-temperature region generated bainite is a structure in which an average interval of retained γ and the like is less than 1 μm when the nital corroded steel sheet cross-section is SEM observed.
Here, the “average interval of retained γ and the like” is an average value of measurement results of distances between center positions of adjacent retained γ grains, distances between center positions of adjacent carbide grains or distances between center positions of adjacent retained γ grains and carbide grains. The distance between center positions means a distance between center positions of retained γ grains and carbide grains obtained when most adjacent retained γ grains and/or carbide grains are measured. The center position is a position where a major axis and a minor axis determined for the retained γ grain or the carbide grain intersect.
Since a plurality of retained γ grains and carbide grains are connected into a needle shape or plate shape if retained γ grains and carbide grains are precipitated on a lath boundary, the distance between center positions is not a distance between retained γ grains and/or between carbide grains, but an interval between lines formed by retained γ grains and/or carbide grains connected in a major axis direction. That is, a distance between laths is the distance between center positions 2.
Further, tempered martensite is a structure having an action similar to the above low-temperature region generated bainite and contributes to an improvement of the local deformability of the steel sheet. Note that since low-temperature region generated bainite and tempered martensite described above cannot be distinguished by SEM observation, the low-temperature region generated bainite and tempered martensite are collectively called “low-temperature region generated bainite and the like” in the present invention.
In the present invention, bainite is distinguished between “high-temperature region generated bainite” and “low-temperature region generated bainite” due to a difference in the generation temperature region and a difference in the average interval of the retained γ and the like as described above because it is difficult to clearly distinguish bainite in general academic structure classification. For example, lath-like bainite and bainitic ferrite are classified into upper bainite and lower bainite according to a transformation temperature. However, in a steel type containing a large amount of Si as much as 1.0% or more as in the present invention, the precipitation of carbide accompanying bainite transformation is suppressed. Thus, it is difficult to distinguish these including the martensite structure in SEM observation. Therefore, in the present invention, bainite is not classified by academic structure definition, but distinguished based on the difference in the generation temperature region and the average interval of the retained γ and the like as described above.
A state of distribution of high-temperature region generated bainite and low-temperature region generated bainite is not particularly limited. Both high-temperature region generated bainite and low-temperature region generated bainite and the like may be generated in former γ grains or high-temperature region generated bainite and low-temperature region generated bainite and the like may be separately generated in each former γ grain.
A state of distribution of high-temperature region generated bainite and low-temperature region generated bainite and the like is diagrammatically shown in
In the present invention, when b denotes an area percent of high-temperature region generated bainite to the entire metal structure and c denotes a total area percent of low-temperature region generated bainite and the like to the entire metal structure, both the area percent b and the area percent c need to satisfy 5 to 40%. Here, the total area percent of low-temperature region generated bainite and tempered martensite is specified instead of the area percent of low-temperature region generated bainite because these structures cannot be distinguished by SEM observation as described above.
The area percent b is set to be 5 to 40%. If a generation amount of high-temperature region generated bainite is too small, the elongation of the steel sheet is reduced and formability cannot be improved. Thus, the area percent b is 5% or higher, preferably 8% or higher and more preferably 10% or higher. However, if the generation amount of high-temperature region generated bainite is excessive, a balance of the generation amount with low-temperature region generated bainite and the like becomes poor and an effect by the compounding of high-temperature region generated bainite and low-temperature region generated bainite and the like is not exhibited. Thus, the area percent b of high-temperature region generated bainite is set to be 40% or lower, preferably 35% or lower, more preferably 30% or lower and even more preferably 25% or lower.
Further, the total area percent c is set to be 5 to 40%. If a generation amount of low-temperature region generated bainite and the like is too small, the local deformability of the steel sheet is reduced and formability cannot be improved. Thus, the total area percent c is 5% or higher, preferably 8% or higher and more preferably 10% or higher. However, if the generation amount of low-temperature region generated bainite and the like is excessive, a balance of the generation amount with high-temperature region generated bainite becomes poor and an effect by the compounding of low-temperature region generated bainite and the like and high-temperature region generated bainite is not exhibited. Thus, the total area percent c of low-temperature region generated bainite and the like is set to be 40% or lower, preferably 35% or lower, more preferably 30% or lower and even more preferably 25% or lower.
A relationship of the area percent b and the total area percent c is not particularly limited if each range satisfies the above range and includes any of a state where b>c, a state where b<c and a state where b=c.
A mixing ratio of high-temperature region generated bainite and low-temperature generated bainite and the like may be determined according to properties required for the steel sheet. Specifically, to further improve local deformability, particularly stretch flange formability (λ) out of the formability of the steel sheet, the ratio of high-temperature region generated bainite may be maximally reduced and the ratio of low-temperature region generated bainite and the like may be maximally increased. On the other hand, to further improve elongation out of the formability of the steel sheet, the ratio of high-temperature region generated bainite may be maximally increased and the ratio of low-temperature region generated bainite and the like may be maximally reduced. Further, to further enhance the strength of the steel sheet, the ratio of low-temperature region generated bainite and the like may be maximally increased and the ratio of high-temperature region generated bainite may be maximally reduced.
Note that, in the present invention, bainite also includes bainitic ferrite. Bainite is a structure in which carbide is precipitated and bainitic ferrite is a structure in which carbide is not precipitated.
[Polygonal Ferrite+Bainite+Tempered Martensite]
In the present invention, the sum of the area percent a of polygonal ferrite, the area b of high-temperature region generated bainite and the total area percent c of the low-temperature region generated bainite and the like (hereinafter, referred to as a “total area percent of a+b+c”) preferably satisfies 70% or higher to the entire metal structure. If the total area percent of a+b+c is below 70%, elongation may be deteriorated. The total area percent of a+b+c is more preferably 75% or higher and even more preferably 80% or higher. An upper limit of the total area percent of a+b+c is determined in consideration of the space factor of retained γ measured by the saturation magnetization method and, for example, 100%.
[Retained γ]
Retained γ has an effect of prompting the hardening of deformed parts and preventing a concentration of distortion by being transformed into martensite when the steel sheet is deformed by receiving stress, whereby homogeneous deformability is improved to exhibit good elongation. Such an effect is generally called a TRIP effect.
To exhibit these effects, a volume percent of retained γ to the entire metal structure needs to be 5 volume % or higher when measured by the saturation magnetization method. Retained γ is preferably 8 volume % or higher and more preferably 10 volume % or higher. However, if a generation amount of retained γ is too much, the MA mixed phases are also excessively generated and easily coarsened. Thus, local deformability, particularly stretch flange formability and bendability are reduced. Thus, an upper limit of retained γ is preferably about 30 volume % or lower and more preferably 25 volume % or lower.
Retained γ is mainly generated between laths of the metal structure, but may be present in the form of lumps as parts of the MA mixed phases to be described later on aggregates of lath-like structures such as blocks, packets and former γ grain boundaries.
[Miscellaneous]
The metal structure of the steel sheet according to the present invention contains polygonal ferrite, bainite, tempered martensite and retained γ as described above and may be composed only of these, but (a) MA mixed phases in which quenched martensite and retained γ are compounded and (b) remaining structures such as perlite may be present without impairing the effect of the present invention.
(a) MA Mixed Phase
The MA mixed phase is generally known as a composite phase of quenched martensite and retained γ and is a structure generated by a part of a structure present as austenite left untransformed before final cooling being transformed into martensite during final cooling and the remaining part of the structure remaining as austenite. The thus generated MA mixed phase is a very hard structure since carbon is condensed into a high concentration during a heating treatment, particularly in the process of an austempering treatment held in the T2 temperature region and a part thereof is transformed into a martensite structure. Thus, a hardness difference between bainite and the MA mixed phase is large and stress concentrates and easily becomes a starting point of void generation in deformation. Thus, if the MA mixed phases are excessively generated, stretch flange formability and bendability are reduced and local deformability is reduced. Further, if the MA mixed phases are excessively generated, strength tends to become excessively high. The MA mixed phases are more easily generated as the amount of retained γ increases and as the content of Si increases, but a generation amount thereof is preferably as small as possible.
The MA mixed phases are preferably 30 area % or less, more preferably 25 area % or less and further preferably 20 area % or less to the entire metal structure when the metal structure is observed by an optical microscope.
A ratio of the number of the MA mixed phases whose circle-equivalent diameter d is larger than 7 μm to the total number of the MA mixed phases is preferably 0% or more and less than 15%. The coarse MA mixed phases whose circle-equivalent diameter d is larger than 7 μm adversely affect local deformability. The ratio of the number of the MA mixed phases whose circle-equivalent diameter d is larger than 7 μm to the total number of the MA mixed phases is more preferably less than 10% and further preferably less than 5%.
The ratio of the number of the MA mixed phases whose circle-equivalent diameter d is larger than 7 μm may be calculated by observing a cross-sectional surface parallel to a rolling direction by the optical microscope.
Note that since it was empirically confirmed that voids were more easily generated as the grain diameter of the MA mixed phases became larger, the circle-equivalent diameter d of the MA mixed phases is recommended to be as small as possible.
(b) Perlite
Perlite is preferably 20 area % or less to the entire metal structure wen the metal structure is SEM observed. If an area percent of perlite exceeds 20%, elongation is deteriorated and it becomes difficult to improve formability. The area percent of perlite is more preferably 15% or less, further preferably 10% or less and even more preferably 5% or less to the entire metal structure.
The above metal structure can be measured in the following procedure.
[SEM Observation]
Polygonal ferrite, high-temperature region generated bainite, low-temperature region generated bainite and the like and perlite can be discriminated if nital corrosion is caused at a ¼ thickness position out of a cross-section of the steel sheet parallel to the rolling direction and SEM-observed at a magnification of about 3000.
Polygonal ferrite is observed as crystal grains containing no white or light gray retained γ and the like described above inside.
High-temperature region generated bainite and low-temperature region generated bainite and the like are mainly observed in gray and as structures in which white or light gray retained γ and the like are dispersed in crystal grains. Thus, according to SEM observation, the area percent of each of high-temperature region generated bainite and low-temperature region generated bainite and the like is calculated as that also including retained γ and the like since high-temperature region generated bainite and low-temperature region generated bainite and the like also contain retained γ and carbide.
In a nital-corroded cross-section of the steel sheet, carbide and retained γ are both observed as white or light gray structures and it is difficult to distinguish the both. Out of these, carbide such as cementite tends to be precipitated in laths rather than between laths as it is generated in a lower temperature region. Thus, it can be thought that carbide was generated in a high temperature region if intervals between carbide grains are wide and generated in a low temperature region if intervals between carbide grains are narrow. Retained γ is normally generated between laths, but the size of the laths is reduced as a generation temperature of the structure becomes lower. Thus, it can be thought that retained γ was generated in a high temperature region if intervals between retained γ grains are wide and generated in a low temperature region if intervals between retained γ grains are narrow. Therefore, in the present invention, when the nital-corroded cross-section is SEM-observed and the distances between center positions of adjacent grains of retained γ and the like are measured, paying attention to retained γ and the like observed in white or light gray in an observation view field, the structure having an average value, i.e. an average interval of 1 μm or more is considered as high-temperature region generated bainite and the structure having an average interval of less than 1 μm is considered as low-temperature region generated bainite and the like.
Perlite is observed as a layered structure of carbide and ferrite.
[Saturation Magnetization Method]
Since the structure of retained γ cannot be identified by SEM observation, the volume percent is measured by the saturation magnetization method. The volume percent of retained γ obtained in this way can be directly read as an area percent. For a detailed measurement principle by the saturation magnetization method, reference may be made to “R&D Kobe Steel Technical Report, Vol. 52, No. 3, 2002, pp. 43 to 46”.
As just described, in the present invention, the volume percent of retained γ is measured by the saturation magnetization method, whereas the area percent of each of high-temperature region generated bainite and low-temperature region generated bainite and the like is measured, including retained γ, by SEM observation. Thus, the sum of these may exceed 100%.
[Optical Microscope Observation]
The MA mixed phase is observed as a white structure when Repera corrosion is caused at a ¼ thickness position out of a cross-section of the steel sheet parallel to the rolling direction and observed at a magnification of about 1000 by an optical microscope.
Next, the IQ (Image Quality) distribution of the high-strength steel sheet according to the present invention is described.
[IQ Distribution]
In the present invention, an area enclosed by a boundary in which a crystal orientation difference between measurement points by EBSD is 3° or larger is defined as a “crystal grain” and each average IQ based on the visibility of an EBSD pattern analyzed for each crystal grain having a body centered cubic lattice (including a body centered tetragonal lattice) is used as IQ. Each average IQ described above may be merely referred to as “IQ” below. The crystal orientation difference is set to be 30 or larger to exclude lath boundaries. Note that since the body centered tetragonal lattice is elongated in one direction by the solid solution of C atoms at specific intrusive positions in the body centered cubic lattice and is equivalent in structure itself to the body centered cubic lattice, effects on low-temperature toughness are also equivalent. Further, these lattices cannot be distinguished even by EBSD. Thus, in the present invention, the measurement of the body centered cubic lattice includes that of the body centered tetragonal lattice.
The IQ is the visibility of the EBSD pattern. The IQ is known to be affected by a distortion amount in the crystal. Specifically, the smaller the IQ, the more distortions tend to exist in the crystal. The present inventors and other researchers pursued studies, paying attention to a relation of the distortion of crystal grains and low-temperature toughness. First, effects on low-temperature toughness were studied from the IQ of each measurement point by EBSD, i.e. a relationship of areas with many distortions and areas with fewer distortions, but no relationship between the IQ of each measurement point and low-temperature toughness was found. On the other hand, effects on low-temperature toughness were studied from the average IQ of each crystal grain, i.e. a relationship of the number of crystals with many distortions and the number of crystal grains with fewer distortions, with the result that it was found that low-temperature toughness could be improved if a control was executed to relatively increase crystal grains with fewer distortions in number with respect to the crystal grains with many distortions. It was found out that, even in a metal structure containing ferrite and retained γ, good low-temperature toughness could be obtained if the IQ distribution of each crystal grain including the body centered cubic lattice (including the body centered tetragonal lattice) of the steel sheet is properly controlled to satisfy the following Equations (1) and (2).
(IQave−IQmin)/(IQmax−IQmin)≧0.40 (1)
(σIQ)/(IQmax−IQmin)≦0.25 (2)
wherein: IQave denotes an average value of average IQ total data of each crystal grain,
The average IQ value of each crystal grain is an average value of the IQ of each crystal grain obtained from the result of EBSD measurements conducted at 180,000 points with one step of 0.25 μm by polishing a cross-section of a sample parallel to a rolling direction and setting an area of 100 μm×100 μm at a ¼ thickness position as a measurement area. Note that the crystal grains partly fragmented on a boundary line of the measurement area are excluded from measurement objects and only the crystal grains completely accommodated in the measurement area are measured.
Further, in IQ analysis, measurement points having a CI (Confidence Index)<0.1 are excluded from the analysis in terms of ensuring reliability. The CI is a degree of confidence of data and an index indicating a degree of coincidence of the EBSD pattern detected at each measurement point with a database value of a designated crystal system, e.g. a body centered cubic lattice or face centered cubic (FCC) lattice in the case of iron.
Further, in the calculation of the above Equations (1) and (2), values excluding 2% of data from the total data on each of maximum and minimum sides are used in terms of excluding abnormal values.
Further, in the above Equations (1) and (2), relativization using IQmin, IQmax is carried out in consideration of a fluctuation of absolute values of the IQs due to the influence of a detector and the like.
IQave and σIQ are indices indicating effects on low-temperature toughness and good low-temperature toughness is obtained if IQave is large and σIQ is small. In terms of ensuring good low-temperature toughness, Equation (1) is 0.40 or larger, preferably 0.42 or larger and more preferably 0.45 or larger. As the value of Equation (1) becomes larger, the crystal grains with fewer distortions increase in number and better low-temperature toughness is obtained. Thus, an upper limit is not particularly limited, but 0.80 or smaller, for example. On the other hand, Equation (2) is 0.25 or smaller, preferably 0.24 or smaller and more preferably 0.23 or smaller. As the value of Equation (2) becomes smaller, the IQ distribution of the crystal grains represented by a histogram becomes sharper and becomes a distribution preferable in improving low-temperature toughness. Thus, a lower limit is not particularly limited, but 0.15 or larger, for example.
In the present invention, excellent low-temperature toughness is obtained by satisfying both Equations (1) and (2).
Qualitatively, low-temperature toughness is improved in a sharp mountain-shaped distribution with many crystal grains peaked on a crystal grain side where the average IQ is large within a range from IQmin to IQmax, i.e. at positions where the value of Equation (1) is 0.40 or larger, i.e. in an IQ distribution in which the value of Equation (2) is 0.25 or smaller as shown in
Next, a chemical component composition of the high-strength steel sheet according to the present invention is described.
<<Component Composition>>
The high-strength steel sheet of the present invention is a steel sheet satisfying C: 0.10 to 0.5%, Si: 1.0 to 3%, Mn: 1.5 to 3.0%, Al: 0.005 to 1.0%, P: more than 0% and not more than 0.1% and S: more than 0% and not more than 0.05% and the balance iron with inevitable impurities. These ranges are determined for the following reason.
[C: 0.10 to 0.5%]
C is an element necessary to enhance the strength of the steel sheet and generate retained γ. Accordingly, the amount of C is not less than 0.10%, preferably not less than 0.13% and more preferably not less than 0.15%. However, if C is excessively contained, weldability is reduced. Thus, the amount of C is not more than 0.5%, preferably not more than 0.3%, more preferably not more than 0.25% and further preferably not more than 0.20%.
[Si: 0.10 to 3%]
Si is an element very important in effectively generating retained γ by suppressing the precipitation of carbide in the T1 temperature region and the T2 temperature region, particularly during the austempering treatment in addition to contributing to increasing the strength of the steel sheet as a solid solution strengthening element. Accordingly, the amount of Si is not less than 1.00%, preferably not less than 1.2% and more preferably not less than 1.3%. However, if Si is excessively contained, reverse transformation into a γ phase does not occur during heating and soaking in annealing and a large amount of polygonal ferrite remains, leading to a shortage of strength. Further, Si scales are generated on a steel sheet surface in hot rolling to deteriorate a surface property of the steel sheet. Thus, the amount of Si is not more than 3%, preferably not more than 2.5% and more preferably not more than 2.0%.
[Mn: 1.5 to 3.0%]
Mn is an element necessary to obtain bainite and tempered martensite. Further, Mn is an element which effectively acts to generate retained γ by stabilizing austenite. To exhibit these actions, the amount of Mn is not less than 1.5%, preferably not less than 1.8% and more preferably not less than 2.0%. However, if Mn is excessively contained, the generation of high-temperature region generated bainite is drastically suppressed. Further, excessive addition of Mn leads to the deterioration of weldability and the deterioration of formability due to segregation. Thus, the amount of Mn is not more than 3.0%, preferably not more than 2.7%, more preferably not more than 2.5% and further preferably not more than 2.4%.
[Al: 0.005 to 1.0%]
Al is, similarly to Si, an element which contributes to the generation of retained γ by suppressing the precipitation of carbide during the austempering treatment. Further, Al is an element which acts as deoxidizer in a steel production process. Thus, the amount of Al is not less than 0.005%, preferably not less than 0.01% and more preferably not less than 0.03%. However, if Al is excessively contained, inclusion in the steel sheet becomes excessive to deteriorate ductility. Thus, the amount of Al is not more than 1.0%, preferably not more than 0.8% and more preferably not more than 0.5%.
[P: More than 0% and not More than 0.1%]
P is an impurity element unavoidably contained in steel. If the amount of P is excessive, the weldability of the steel sheet is deteriorated. Thus, the amount of P is not more than 0.1%, preferably not more than 0.08% and more preferably not more than 0.05%. Although the amount of P is preferably as small as possible, it is industrially difficult to set the amount of P at 0%.
[S: More than 0% and not More than 0.05%]
S is an impurity element unavoidably contained in steel and, similarly to P described above, an element which deteriorates the weldability of the steel sheet. Further, S forms sulfide-based inclusion in the steel sheet and formability is reduced if this sulfide-based inclusion increases. Thus, the amount of S is not more than 0.05%, preferably not more than 0.01% and more preferably not more than 0.005%. Although the amount of S is preferably as small as possible, it is industrially difficult to set the amount of S at 0%.
The high-strength steel sheet according to the present invention satisfies the above component composition and the balance components are iron and inevitable impurities other than P, S described above. Inevitable impurities include, for example, N, O (oxygen) and tramp elements such as Pb, Bi, Sb and Sn. Out of inevitable impurities, the amount of N is preferably more than 0% and not more than 0.01% and the amount of O is preferably more than 0% and not more than 0.01%.
[N: More than 0% and not More than 0.01%]
N is an element which contributes to the strengthening of the steel sheet by causing nitride to precipitate in the steel sheet. If N is excessively contained, a large amount of nitride precipitates to deteriorate elongation, stretch flange formability and bendability. Thus, the amount of N is preferably not more than 0.01%, more preferably not more than 0.008% and further preferably not more than 0.005%.
[O: More than 0% and not More than 0.01%]
O is an element which causes a reduction in elongation, stretch flange formability and bendability when being excessively contained. Thus, the amount of O is preferably not more than 0.01%, more preferably not more than 0.005% and further preferably not more than 0.003%.
The steel sheet of the present invention may further contain as other elements:
(a) One or more elements selected from a group consisting of Cr: more than 0% and not more than 1% and Mo: more than 0% and not more than 1%,
(b) One or more elements selected from a group consisting of Ti: more than 0% and not more than 0.15%, Nb: more than 0% and not more than 0.15% and V: more than 0% and not more than 0.15%,
(c) One or more elements selected from a group consisting of Cu: more than 0% and not more than 1% and Ni: more than 0% and not more than 1%,
(d) B: more than 0% and not more than 0.005%,
(e) One or more elements selected from a group consisting of Ca: more than 0% and not more than 0.01%, Mg: more than 0% and not more than 0.01% and rare-earth elements: more than 0% and not more than 0.01%.
(a) [One or More Elements Selected from Group Consisting of Cr: More than 0% and not More than 1% and Mo: More than 0% and not More than 1%]
Cr and Mo are elements which effectively act to obtain bainite and tempered martensite similarly to Mn described above. These elements can be used singly or in combination. To effectively exhibit this action, the single content of each of Cr and Mo is preferably not less than 0.1% and more preferably not less than 0.2%. However, if the content of each of Cr and Mo exceeds 1%, the generation of high-temperature region generated bainite is drastically suppressed. Further, excessive addition leads to a cost increase. Thus, the content of each of Cr and Mo is preferably not more than 1%, more preferably not more than 0.8% and further preferably not more than 0.5%. In the case of using Cr and Mo in combination, a total amount is recommended to be not more than 1.5%.
(b) [One or More Elements Selected from Group Consisting of Ti; More than 0% and not More than 0.15%, Nb: More than 0% and not More than 0.15% and V: More than 0% and not More than 0.15%]
Ti, Nb and V are elements which act to strengthen the steel sheet by forming precipitates such as carbide and nitride in the steel sheet and refine polygonal ferrite grains by refining former γ grains. To effectively exhibit these actions, the single content of each of Ti, Nb and V is preferably not less than 0.01% and more preferably not less than 0.02%. However, excessive content leads to the precipitation of carbide in grain boundaries and the deterioration of the stretch flange formability and bendability of the steel sheet. Thus, the single content of each of Ti, Nb and V is preferably not more than 0.15%, more preferably not more than 0.12% and further preferably not more than 0.1%. Each of Ti, Nb and V may be singly contained or two or more elements arbitrarily selected may be contained.
(c) [One or More Elements Selected from Group Consisting of Cu; More than 0% and not More than 1% and Ni: More than 0% and not More than 1%]
Cu and Ni are elements which effectively act to generate retained γ by stabilizing T. These elements can be used singly or in combination. To effectively exhibit this action, the single content of each of Cu and Ni is preferably not less than 0.05% and more preferably not less than 0.1%. However, if Cu and Ni are excessively contained, hot formability is deteriorated. Thus, the single content of each of Cu and Ni is preferably not more than 1%, more preferably not more than 0.8% and further preferably not more than 0.5%. Note that hot formability is deteriorated if the content of Cu exceeds 1%, but the deterioration of hot formability is suppressed if Ni is added. Thus, more than 1% of Cu may be added, although it leads to a cost increase, in the case of using Cu and Ni in combination.
(d) [B: More than 0% and not More than 0.005%]
B is an element which effectively acts to generate bainite and tempered martensite, similarly to Mn, Cr and Mo described above. To effectively exhibit this action, the content of B is preferably not less than 0.0005% and more preferably not less than 0.001%. However, if B is excessively contained, boride is generated in the steel sheet to deteriorate ductility. Further, if B is excessively contained, the generation of high-temperature region generated bainite is drastically suppressed, similarly to Cr and Mo described above. Thus, the content of B is preferably not more than 0.005%, more preferably not more than 0.004% and further preferably not more than 0.003%.
(e) [One or More Elements Selected from Group Consisting of Ca; More than 0% and not More than 0.01%, Mg: More than 0% and not More than 0.01% and Rare-Earth Elements: More than 0% and not More than 0.01%]
Ca, Mg and rare-earth elements (REM) are elements which act to finely disperse inclusion in the steel sheet. To effectively exhibit this action, the single content of each of Ca, Mg and rare-earth elements is preferably not less than 0.0005% and more preferably not less than 0.001%. However, excessive content leads to difficulty to produce by deteriorating castability, hot formability and the like. Further, excessive addition causes the deterioration of the ductility of the steel sheet. Thus, the single content of each of Ca, Mg and rare-earth elements is preferably not more than 0.01%, more preferably 0.005% and further preferably not more than 0.003%.
The rare-earth elements mean to include lanthanoid elements (15 elements from La to Lu) and Sc (scandium) and Y (yttrium). Out of these elements, it is preferable to contain at least one element selected from a group consisting of La, Ce and Y and more preferable to contain La and/Ce.
The metal structure and component composition of the high-strength steel sheet according to the present invention are described above.
<<Producing Method>>
Next, a producing method of the above high-strength steel sheet is described. The above high-strength steel sheet can be produced by successively performing a step of heating a steel sheet satisfying the component composition to a two-phase temperature region of 800° C. or higher and an Ac3 point—10° C. or lower, a step of holding and soaking the steel sheet in this temperature region for 50 seconds or longer, a step of cooling the steel sheet at an average cooling rate of 20° C. or lower in a range of 600° C. or higher and then cooling the steel sheet at an average cooling rate of 10° C. or higher up to an arbitrary temperature T satisfying 150° C. or higher and 400° C. or lower (an Ms point or lower when the Ms point is 400° C. or lower), a step of holding the steel sheet in the T1 temperature region satisfying the following Equation (3) for 10 to 200 seconds and a step of holding the steel sheet in the T2 temperature region satisfying the following Equation (4) for 50 seconds or longer. Each step is successively described below.
150° C.≦T1(° C.)≦400° C. (3)
400° C.<T2(° C.)≦540° C. (4)
[Hot Rolling and Cold Rolling]
First, a slab is hot rolled in accordance with a conventional method and the obtained hot rolled steel sheet is cold rolled to prepare a cold rolled steel sheet. In hot rolling, a finish rolling temperature may be, for example, set at 800° C. or higher and a winding temperature may be, for example, set at 700° C. or lower. In cold rolling, rolling may be performed with a cold rolling rate set, for example, in a range of 10 to 70%.
[Soaking]
The cold rolled steel sheet obtained in this way is subjected to the soaking step.
Specifically, the steel sheet is heated to the temperature region of 800° C. or higher and the Ac3 point—10° C. or lower and soaked by being held in this temperature region for 50 seconds longer in a continuous annealing line.
By controlling a heating temperature to a two-phase temperature region of ferrite and austenite, a predetermined amount of polygonal ferrite can be generated. If the heating temperature is too high, it leads to an austenite single phase region and the generation of polygonal ferrite is suppressed. Thus, the elongation of the steel sheet cannot be improved and formability is deteriorated. Accordingly, the heating temperature is the Ac3 point—10° C. or lower, preferably the Ac3 point—15° C. or lower and more preferably the Ac3 point—20° C. or lower. On the other hand, if the heating temperature falls below 800° C., a wrought structure due to cold rolling remains and reverse transformation into austenite does not progress. Thus, desired elongation, stretch flange formability and the like are adversely affected. Therefore, the heating temperature is 800° or higher, preferably 810° C. or higher and more preferably 820° or higher.
A soaking time during which the steel sheet is held in the above temperature region is 50 seconds or longer. If the soaking time is shorter than 50 seconds, the steel sheet cannot be uniformly heated. Thus, carbide remains in a solid solution state, the generation of retained γ is suppressed and reverse transformation into austenite does not progress. Thus, it finally becomes difficult to ensure fractions of bainite and tempered martensite and formability cannot be improved. Accordingly, the soaking time is set to be 50 seconds or longer, preferably 100 seconds or longer. However, if the soaking time is too long, austenite grain diameters become large and, associated with that, polygonal ferrite grains are also coarsened, whereby elongation and local deformability tend to be worsened. Therefore, the soaking time is preferably 500 seconds or shorter and more preferably 450 seconds or shorter.
Note that an average heating rate when the above cold rolled steel sheet is heated to the two-phase temperature region may be set, for example, at 1° C./s or higher.
The Ac3 point can be calculated from the following Equation (a) described in “The Physical Metallurgy of Steels” by Leslie (issued on May 31, 1985 by Maruzen Co., Ltd., P. 273). In the following Equation (a), [ ] indicates a content (mass %) of each element and the content of the element not contained in the steel sheet may be calculated as 0 mass %.
Ac3(° C.)=910−203×[C]1/2+44.7×[Si]−30×[Mn]−11×[Cr]+31.5×[Mo]−20×[Cu]−15.2×[Ni]+400×[Ti]+104×[V]+700×[P]+400×[Al] (a)
[Cooling Step]
After the steel sheet is heated to the two-phase temperature region and soaked while being held for 50 seconds or longer, it is gradually cooled at an average cooling rate of 20° C./s or lower in the range of 600° C. or higher. Hereinafter, the average cooling rate in the range of 600° C. or higher is referred to as “CR1” in some cases. By properly controlling the average cooling rate in this range, it is possible to generate martensite effective in promoting the generation of low-temperature region generated bainite and high-temperature region generated bainite while ensuring a predetermined amount of polygonal ferrite.
Further, if the average cooling rate in the range of 600° C. or higher exceeds 20° C./s, the predetermined amount of polygonal ferrite cannot be ensured and elongation is reduced. Thus, the average cooling rate is 20° C./s or lower, preferably 15° C./s or lower and more preferably 10° C./s or lower.
Thereafter, the steel sheet is quickly cooled at an average cooling rate of 10° C./s or higher up to the arbitrary temperature T satisfying 150° C. or higher and 400° C. or lower (Ms point or lower when the Ms point is 400° C. or lower). The above T may be referred to as a “cooling stop temperature T” in some cases below. Further, an average cooling rate in the range from below 600° C. to the cooling stop temperature T is written as “CR2” in some cases below.
If the cooling stop temperature T falls below 150° C., the generation amount of martensite increases, whereby a desired metal structure cannot be obtained and elongation, stretch flange formability, complex formability evaluated in an Erichsen test and the like are deteriorated. The cooling stop temperature T is 150° C. or higher, preferably 160° C. or higher and more preferably 170° C. or higher. On the other hand, if the cooling stop temperature T exceeds 400° C. (if the cooling stop temperature T exceeds the Ms point when the Ms point is lower than 400° C.), martensite is not generated and the compounding of the bainite structure and the refining of the Ma mixed phases are not realized. Thus, elongation, stretch flange formability, bendability and complex formability evaluated in the Erichsen test are deteriorated. Further, if the cooling stop temperature T is too high, IQave decreases and σIQ increases, whereby it may not be possible to obtain the low-temperature toughness improving effect. The cooling stop temperature T is 400° C. or lower (Ms point or lower if the Ms point is lower than 400° C.), preferably 380° C. or lower (below Ms point—20° C. or lower if the Ms point—20° C. is lower than 380° C.) and more preferably 350° C. or lower (Ms point—50° C. or lower if the Ms point—50° C. is lower than 350° C.).
Note that, in the present invention, the Ms point can be calculated from the following Equation (b) obtained considering a ferrite fraction from an equation described in “The Physical Metallurgy of Steels” by Leslie P. 231). In the present invention, prior to the production of a steel material, the Ms point may be calculated using a steel material having the same composition and the cooling stop temperature T may be set in advance.
Ms point(° C.)=561−474×[C]/(1−Vf/100)−33×[Mn]−17×[Ni]−17×[Cr]−21×[Mo] (b)
Here, Vf denotes a ferrite fraction measurement value (area %) in a sample representing an annealing pattern from heating, soaking to cooling when the sample is separately fabricated. Further, in Equation, [ ] indicates a content (mass %) of each element and the content of the element not contained in the steel sheet may be calculated as 0 mass %.
If the average cooling rate from the two-phase temperature region to the cooling stop temperature T falls below 10° C./s, perlite transformation occurs to excessively generate perlite, whereas the amount of retained γ becomes insufficient, elongation is reduced and formability is deteriorated. Thus, the average cooling rate of the temperature region from below 600° C. to the cooling stop temperature T (hereinafter, referred to as a “temperature region below 600° C.” in some cases) is 10° C./s or higher, preferably 15° C./s or higher and more preferably 20° C./s or higher. An upper limit of the average cooling rate of the temperature region below 600° C. is not particularly limited. However, since a temperature control is difficult if the average cooling rate is excessively increased, the upper limit may be, for example, about 100° C./s.
Note that a relationship of CR1 and CR2 is not particularly limited. They may be the same cooling rate if satisfying the predetermined average cooling rate, but it is desirable in terms of obtaining a desired metal structure to preferably control the cooling rate to satisfy a relationship of CR2>CR1.
[Annealing Condition after Cooling]
After cooling to the cooling stop temperature T, the steel sheet is heated to the T2 temperature region satisfying the above Equation (4) and held in this T2 temperature region for 50 seconds or longer after being held in the T1 temperature region satisfying the above Equation (3) for 10 to 200 seconds or longer. In the present invention, by properly controlling the respective holding times in the T1 temperature region and in the T2 temperature region, it is possible to generate a predetermined amount of each of high-temperature region generated bainite and low-temperature region generated bainite and the like. Specifically, by holding the steel sheet in the T1 temperature region for a predetermined time, untransformed austenite is transformed into low-temperature region generated bainite or martensite. By the austempering treatment for holding the steel sheet in the T2 temperature region for the predetermined time, untransformed austenite is transformed into high-temperature region generated bainite, the generation amount thereof is controlled and carbon is condensed into austenite to generate retained γ, whereby the desired metal structure and the IQ distribution specified in the present invention can be realized.
Further, by combining the holding in the T1 temperature region and the holding in the T2 temperature region, an effect of being able to suppress the generation of the MA mixed phases is also exhibited. Specifically, by cooling the steel sheet at the above predetermined average cooling rate up to the cooling stop temperature T and holding it in the T1 temperature region after soaking the steel sheet at the predetermined temperature, martensite and low-temperature region generated bainite are generated, wherefore untransformed parts are refined and the condensation of carbon into the untransformed parts is suppressed. Thus, the MA mixed phases are refined.
Note that since the size of the lath-like structure becomes smaller in the case of cooling the steel sheet at the predetermined cooling rate from the soaking temperature to the cooling stop temperature T and holding the steel sheet only in the T1 temperature region satisfying the above Equation (3) without heating the steel sheet to the T2 temperature region satisfying the above Equation (4) and holding it in that temperature region, i.e. even if the austempering treatment is simply performed for holding at a low temperature, the MA mixed phases themselves can be made smaller. However, in this case, since the steel sheet is not held in the above T2 temperature region, high-temperature region generated bainite is hardly generated, a dislocation density of the lath-like structure of a base becomes large and strength is excessively increased to reduce elongation and IQave.
[Cooling Stop Temperature]
In the present invention, the T1 temperature region specified by the above Equation (3) is specifically 150° or higher and 400° C. or lower. By holding the steel sheet in this temperature region for a predetermined time, untransformed austenite can be transformed into low-temperature region generated bainite or martensite. Further, by ensuring a sufficient holding time, bainite transformation progresses and, finally, retained γ is generated and the MA mixed phases are refined. This martensite exists as quenched martensite immediately after transformation, but is tempered while being held in the T2 temperature region to be described later and remains as tempered martensite. This tempered martensite adversely affects none of the elongation, stretch flange formability and bendability of the steel sheet.
However, if the holding temperature is above 400° C., predetermined amounts of low-temperature region generated bainite and martensite are not generated and the bainite structure cannot be compounded. Further, the MA mixed phases cannot be refined, local deformability is reduced and stretch flange formability and bendability cannot be improved. Thus, the T1 temperature region is 400° C. or lower, preferably 380° C. or lower and further preferably 350° C. or lower. On the other hand, if the holding temperature is below 150° C., a martensite fraction becomes excessively large, wherefore elongation and complex formability in the Erichsen test are deteriorated. Thus, a lower limit of the T1 temperature region is 150° C. or higher, preferably 160° C. or higher and more preferably 170° C. or higher.
[Holding after Cooling]
The holding time in the T1 temperature region satisfying the above Equation (3) is 10 to 200 seconds. If the holding time in the T1 temperature region is too short, the generation amount of low-temperature region generated bainite is reduced, the compounding of the bainite structure and the refining of the MA mixed phases cannot be realized. Thus, elongation and stretch flange formability are reduced. Further, σIQ increases as IQave is reduced, and desired low-temperature toughness may not be obtained. Thus, the holding time in the T1 temperature region is 10 seconds or longer, preferably 15 seconds or longer, more preferably 30 seconds or longer and further preferably 50 seconds or longer. However, since low-temperature region generated bainite is excessively generated if the holding time exceeds 200 seconds, the generation amounts of high-temperature region generated bainite and the like cannot be ensured and the amount of retained γ also becomes insufficient even if the steel sheet is held in the T2 temperature region for the predetermined time, wherefore elongation, complex formability in the Erichsen test and the like are deteriorated. Thus, the holding time in the T1 temperature region is 200 seconds or shorter, preferably 180 seconds or shorter and more preferably 150 seconds or shorter.
In the present invention, the holding time in the T1 temperature region means a time until the surface temperature of the steel sheet reaches 400° C. again by starting heating after the steel sheet is held in the T1 temperature region after the surface temperature of the steel sheet reaches 400° C. (Ms point if the Ms point is 400° C. or lower) by cooling the steel sheet after soaking it at the predetermined temperature. For example, the holding time in the T1 temperature region is a time of a section “x” in
The method for holding the steel sheet in the T1 temperature region satisfying the above Equation (3) is not particularly limited if the holding time in the T1 temperature region is 10 to 200 seconds. For example, heat patterns shown in (i) to (iii) of
Out of these, (i) of
(iii) of
(iii) of
[Reheating and Holding]
In the present invention, the T2 temperature region specified by the above Equation (4) is specifically higher than 400° C. and not higher than 540° C. By holding the steel sheet in this temperature region for a predetermined time, high-temperature region generated bainite and retained γ can be generated. Further, although effects of the holding temperature in the T2 temperature region on the IQ distribution are not clear, a desired IQ distribution is obtained by holding the steel sheet in the above T2 temperature region. If the steel sheet is held at a temperature higher than 540° C., polygonal ferrite and pseudo perlite are generated, a desired metal structure cannot be obtained and elongation and the like cannot be ensured. Thus, an upper limit of the T2 temperature region is 540° C. or lower, preferably 500° C. or lower and more preferably 480° C. or lower. On the other hand, at 400° C. or lower, the amount of high-temperature region generated bainite becomes insufficient and carbon condensation into untransformed parts accompanying bainite transformation also becomes insufficient to reduce the amount of retained γ. Thus, elongation and complex formability in the Erichsen test are reduced. Thus, the lower limit of the T2 temperature region is 400° C. or higher, preferably 420° C. or higher and more preferably 425° C. or higher.
The holding time in the T2 temperature region satisfying the above Equation (4) is 50 seconds or longer. According to the present invention, even if the holding time in the T2 temperature region is set at about 50 seconds, the generation of high-temperature region generated bainite is promoted by low-temperature region generated bainite and the like since low-temperature region generated bainite and the like are generated by holding the steel sheet in the above T1 temperature region for the predetermined time in advance. Thus, the generation amount of the high-temperature region generated bainite can be ensured. However, if the holding time is shorter than 50 seconds, many untransformed parts remain and carbon condensation is insufficient, wherefore hard quenched martensite is generated during final cooling from the T2 temperature region. Thus, many coarse MA mixed phases are generated, strength is excessively increased to reduce elongation and local deformability such as stretch flange formability and bendability is drastically reduced. Further, if the holding time in the T2 temperature region is short, IQave tends to decrease. To obtain the desired IQ distribution, it is effective to set the holding time at 50 seconds or longer. In terms of improving productivity, the holding time in the T2 temperature region is as short as possible. However, to reliably generate high-temperature region generated bainite, the holding time is preferably set at 90 seconds or longer and more preferably set at 120 seconds or longer. An upper limit of the holding time in the T2 temperature region is not particularly limited, but the generation of high-temperature region generated bainite is saturated and productivity is reduced even if the steel sheet is held in this temperature region for a long time. Further, condensed carbon precipitates as carbide, retained γ cannot be ensured and elongation is deteriorated. Thus, the holding time in the T2 temperature region is preferably 1800 seconds or shorter, more preferably 1500 seconds or shorter and further preferably 1000 seconds or shorter.
Further, the holding time in the T2 temperature region means a time until the surface temperature of the steel sheet reaches 400° C. again by starting cooling after the steel sheet is held in the T2 temperature region after the surface temperature of the steel sheet reaches 400° C. (Ms point if the Ms point is 400° C. or lower) by heating the steel sheet after holding it in the T1 temperature region. For example, the holding time in the T2 temperature region is a time of a section “y” in
The method for holding the steel sheet in the T2 temperature region satisfying the above Equation (4) is not particularly limited if the residence time in the T2 temperature region is 50 seconds or longer. The steel sheet may be held at an arbitrary constant temperature in the T2 temperature region as in the heat patterns in the above T1 temperature region or may be cooled or heated in the T2 temperature region.
Note that the steel sheet is held in the T2 temperature region on a high temperature side after being held in the T1 temperature region on a low temperature side in the present invention. However, the present inventors and other researchers have confirmed that, although low-temperature region generated bainite and the like generated in the T1 temperature region are heated to the T2 temperature region and a lower structure is recovered by tempering, lath intervals, i.e. average intervals of retained γ and/or carbide do not change.
[Plating]
An electro-galvanized (EG) layer, a hot dip galvanized (GI) layer or an alloyed hot dip galvanized (GA) layer may be formed on the surface of the high-strength steel sheet.
Formation conditions of the electro-galvanized layer, the hot dip galvanized layer or the alloyed hot dip galvanized layer are not particularly limited, and a conventional electro-galvanizing treatment, hot dip galvanizing treatment or alloying treatment can be adopted. In this way, an electro-galvanized steel sheet (hereinafter, referred to as an “EG steel sheet” in some cases), a hot dip galvanized steel sheet (hereinafter, referred to as a “GI steel sheet” in some cases) and an alloyed hot dip galvanized steel sheet (hereinafter, referred to as a “GA steel sheet” in some cases) are obtained.
In the case of producing an EG steel sheet, a method is, for example, adopted in which a current is applied while the above steel sheet is immersed in a zinc solution of 55° C., and the steel sheet is cooled.
In the case of producing a GI steel sheet, a method is, for example, adopted in which hot dip galvanizing is applied by immersing the above steel sheet in a plating bath whose temperature is adjusted to about 430 to 500° C. and, thereafter, the steel sheet is cooled.
In the case of producing a GA steel sheet, a method is, for example, adopted in which the above steel sheet is heated to a temperature of about 500 to 540° to be alloyed after the above hot dip galvanizing, and is cooled.
Further, in the case of producing a GI steel sheet, hot dip galvanizing may be applied by immersing the steel sheet in the plating bath regulated to the aforementioned temperature region in the above T2 temperature region without being cooled to a room temperature after being held in the above T2 temperature region and, thereafter, the steel sheet may be cooled. In the case of producing a GA steel sheet, the alloying treatment may be applied following hot dip galvanizing in the above T2 temperature region. In this case, a time required for hot dip galvanizing and a time required for the alloying treatment may be controlled while being included in the holding time in the above T2 temperature region.
Further, in the case of producing a GI steel sheet, the hot dip galvanizing treatment may be performed together with a step of holding the steel sheet in the above T2 temperature region after holding the steel sheet in the above T1 temperature region. Specifically, after the steel sheet is held in the T1 temperature region, hot dip galvanizing may be applied by immersing the steel sheet in the plating bath regulated to the aforementioned temperature region in the above T2 temperature region, thereby performing both hot dip galvanizing and holding in the T2 temperature region. Further, in the case of producing a GA steel sheet, the alloying treatment may be performed following hot dip galvanizing in the above T2 temperature region.
The coating weight of electro-galvanizing is also not particularly limited and may be, for example, about 10 to 100 g/m2 per surface.
[Fields of Application of High-Strength Steel Sheet of Present Invention]
The technology of the present invention can be suitably adopted for thin steel sheets having a sheet thickness of 3 mm or smaller. Since the high-strength steel sheet according to the present invention has a tensile strength of 590 MPa or more and is excellent in elongation and good in local deformability and low-temperature toughness, formability is excellent. Further, low-temperature toughness is also good and brittle fracture, for example, under a low temperature environment of −20° C. or lower can be suppressed. This high-strength steel sheet is suitably used as a material of structural components of automotive vehicles. Examples of structural components of automotive vehicles are reinforcing members such as pillars (e.g. center pillar reinforces), reinforcing members for roof rails, vehicle body constituent components such as side sills, floor members and kick portions, impact resistant absorbing components such as reinforcing members for bumpers and door impact beams and seat components, including collision components such as front and rear side members and crash boxes.
Further, since the above high-strength steel sheet is good in hot formability, it can be suitably used as a material for hot molding. Note that hot molding means molding in a temperature range of about 50 to 500° C.
This application claims the benefit of the priority based on Japanese Patent Application No. 2013-202537 filed with the Japan Patent Office on Sep. 27, 2013 and Japanese Patent Application No. 2014-071906 filed with the Japan Patent Office on Mar. 31, 2014. The entire contents of the specifications of Japanese Patent Application No. 2013-202537 filed on Sep. 27, 2013 and Japanese Patent Application No. 2014-071906 filed on Mar. 31, 2014 are incorporated herein for reference.
The present invention is specifically described by way of examples below. However, the present invention is not limited by the following examples and can be, of course, carried out while being suitably changed within the range conformable to the gist described above and below. Any of those is encompassed in the technical scope of the present invention.
Steels having chemical component compositions shown in Table 1 below with the balance Iron and inevitable impurities other than P, S, N and O were vacuum-smelted to produce slabs for experiment. In Table 1 below, misch metal containing about 50% of La and about 30% of Ce was used as REM.
The Ac3 point was calculated based on the chemical components shown in Table 1 below and the above Equation (a) and the Ms point was calculated based on the chemical components and the above Equation (b). Since reverse transformation did not progress and carbide remained and, hence, a specified structure could not be secured in No. D-3, the Ms point was not calculated (“*” in Table 2).
The obtained slab for experiment was cold rolled after being hot rolled and, subsequently, continuously annealed to produce a sample. Specific conditions are as follows.
After the slab for experiment was heated and held at 1250° C. for 30 minutes, a pressure reduction ratio was set at about 90%, hot rolling was so performed that a finish rolling temperature became 920° C. and the slab was cooled up to a winding temperature of 500° C. at an average cooling rate of 30° C./s from the finish rolling temperature and wound. After winding the slab was held at the winding temperature of 500° C. for 30 minutes and, subsequently, furnace-cooled up to a room temperature to produce a hot rolled steel sheet having a sheet thickness of 2.6 mm.
After the obtained hot rolled steel sheet was washed with acid and surface scales were removed, cold rolling was performed at a cold rolling rate of 46% to produce a cold rolled steel sheet having a sheet thickness of 1.4 mm.
The obtained cold rolled steel sheet was continuously annealed in accordance with a pattern i to iii shown in Table 2 to produce a sample after being heated to a “soaking temperature (° C.)” shown in Table 2 below and held and soaked for a “soaking time (s)” shown in Table 2. Note that a pattern such as step cooling different from the patterns i to iii was applied for some cold rolled steel sheets. For these, “-” is written in a column of “Pattern” in Table 2. Further, after soaking, the average cooling rate in the range of 600° C. or higher was set at a “gradual cooling rate (° C./s)”.
(Pattern i: Corresponding to (i) of
After soaking, the steel sheet was cooled at the average cooling rate shown in Table 2, i.e. at the “gradual cooling rate (° C./s)” in the range of 600° C. or higher and cooled up to the “cooling stop temperature T (° C.)” shown in Table 2 at a “rapid cooling rate (° C./s)” in a range from below 600° C. to the cooling stop temperature T, then held at this constant cooling stop temperature T for a “holding time (s) in T1” shown in Table 2, subsequently heated up to a “holding temperature (° C.)” in the T2 temperature region shown in Table 2 and held at this holding temperature for a “holding time at holding temperature (s)” shown in Table 2.
(Pattern ii: Corresponding to (ii) of
Similarly to the pattern i, after soaking, the steel sheet was cooled up to the “cooling stop temperature T (° C.)” at the average cooling rate (“gradual cooling rate (° C./s)” and “rapid cooling rate (° C./s)”) shown in Table 2, then cooled from this cooling stop temperature T to an “end temperature (° C.)” in the T1 temperature region shown in Table 2 for the “holding time (s)” in the above T1 temperature region, subsequently heated up to the “holding temperature (° C.)” in the T2 temperature region shown in Table 2 and held at this holding temperature for a “holding time at holding temperature (s)” shown in Table 2.
(Pattern iii: Corresponding to (iii) of
Similarly to the pattern i, after soaking, the steel sheet was cooled up to the “cooling stop temperature T (° C.)” at the average cooling rate (“gradual cooling rate (° C./s)” and “rapid cooling rate (° C./s)”) shown in Table 2, then heated from this cooling stop temperature T to the “end temperature (° C.)” in the T1 temperature region shown in Table 2 for the “holding time (s)” in the above T1 temperature, subsequently heated up to the “holding time (° C.)” in the T2 temperature region shown in Table 2 and held at this holding temperature for the “holding time at holding temperature (s)” shown in Table 2.
In Table 2, a time (s) until the holding temperature in the T2 temperature region was reached after the holding in the T1 temperature region was completed is also shown as “a time (s) of T1→T2”. Further, the “holding time (s) in T1 temperature region” corresponding to the residence time in the section “x” in
Note that although the “rapid cooling stop temperature T (° C.)” and “end temperature (° C.)” in the T1 temperature region and the “holding temperature (° C.)” in the T2 temperature region are deviated from the T1 temperature region or the T2 temperature region specified in the present invention in some of the examples shown in Table 2, temperature was written in each field to show the heat pattern for convenience of description.
For example, a sample 5 using steel type A (abbreviated as “No. A-5” below. The same holds true for other examples) is an example in which the sample was immediately heated to the T2 temperature region for the “holding time in T1” of 0 second, i.e. without being held in the T1 temperature region after being cooled up to the “rapid cooling stop temperature T” of 460° C. exceeding the T1 temperature region specified in the present invention after soaking as shown in Table 2.
For some of the samples obtained by continuous annealing, a plating treatment described below was applied to obtain EG steel sheets, GA steel sheets and GI steel sheets after being cooled up to the room temperature.
[Electro-Galvanizing (EG) Treatment]
After the electro-galvanizing treatment was applied at a current density of 30 to 50 A/dm2 to the sample immersed in an electro-galvanizing bath of 55° C., the sample was washed with water and dried to obtain an EG steel sheet. A galvanizing coating weight was set at 10 to 100 g/m2 per surface.
[Hot Dip Galvanizing (GI) Treatment]
After the plating treatment was applied to the sample immersed in a hot dip galvanizing bath of 450° C., the sample was cooled to the room temperature to obtain a GI steel sheet. A hot dip galvanizing coating weight was set at 10 to 100 g/m2 per surface.
[Alloyed Hot Dip Galvanizing (GA) Treatment]
After being immersed in the hot dip galvanizing bath, the alloying treatment was further applied at 500° C. and, then, the sample was cooled to the room temperature to obtain a GA steel sheet.
Note that No. K-1 is an example in which the hot dip galvanizing (GI) treatment was subsequently applied in the T2 temperature region without cooling after the steel sheet was continuously annealed in accordance with a predetermined pattern. Specifically, hot dip galvanizing was subsequently applied to the sample immersed in the hot dip galvanizing bath of 460° C. for 5 seconds without cooling after being held at the “holding temperature (° C.)” in the T2 temperature region shown in Table 2 for the “holding time at holding temperature (s)”, subsequently the sample was cooled at an average cooling rate of 5° C./s up to the room temperature after being gradually cooled up to 440° C. for 20 seconds.
Further, Nos. 1-1 and M-4 are examples in which hot dip galvanizing and the alloying treatment were subsequently applied in the T2 temperature region without cooling after the samples were continuously annealed in accordance with a predetermined pattern. Specifically, hot dip galvanizing was subsequently applied to the sample immersed in the hot dip galvanizing bath of 460° C. for 5 seconds without cooling after being held at the “holding temperature (° C.)” in the T2 temperature region shown in Table 2 for the “holding time at holding temperature (s)”, subsequently the sample was heated to 500° C. and held at this temperature for 20 seconds to apply the alloying treatment and then cooled at an average cooling rate of 5° C./s up to the room temperature.
In the above plating treatment, degreasing through immersion in alkaline solution, a cleaning treatment such as washing with water or acid were appropriately performed.
Classification of the obtained samples is shown in a column of “Cold Rolled/Plating Classification” of Tables 2 and 3 below. In Tables 2 and 3, “Cold Rolled” indicates a cold rolled steel sheet, “EG” indicates an EG steel sheet, “GI” indicates a GI steel sheet and “GA” indicates a GA steel sheet.
The observation of a metal structure and the evaluation of mechanical properties were conducted in the following procedure for the obtained samples (mean to include cold rolled steel sheets, EG steel sheets, GI steel sheets and GA steel sheets. The same applies to the following.)
<<Observation of Metallic Structure>>
Out of the metal structure, an area percent of each of polygonal ferrite, high-temperature region generated bainite and low-temperature region generated bainite and the like was calculated based on an SEM observation result and a volume percent of retained γ was measured by the saturation magnetization method.
[Structure Fractions of Polygonal Ferrite, High-Temperature Region Generated Bainite and Low-Temperature Region Generated Bainite and the Like]
After a surface of a cross-section of the sample parallel to a rolling direction was polished and further electropolished, nital corrosion was caused and five view fields at a ¼ thickness position were observed at a magnification of 3000 by an SEM. The view fields were about 50 μm×about 50 μm.
Subsequently, average intervals of retained γ and carbide observed in white or light gray were measured based on the aforementioned method in the observation view fields. The area percent of each of high-temperature region generated bainite and low-temperature region generated bainite and the like distinguished by these average intervals was measured by point arithmetic.
An area percent a (area %) of polygonal ferrite, an area percent b (area %) of high-temperature region generated bainite and a total area percent c (area %) of low-temperature region generated bainite and tempered martensite are shown in Table 3 below. In Table 3, B denotes bainite, M denotes martensite and PF denotes polygonal ferrite. Further, the total area percent (area %) of the area percent a, the area percent b and the total area percent c is also shown.
Further, circle-equivalent diameters of polygonal ferrite grains confirmed in the observation view fields were measured and an average value was obtained. A result is shown in a column of “PF Grain Diameter (μm)” of Table 3 below.
[Volume Ratio of Retained γ]
Out of the metal structure, the volume percent of retained γ was measured by the saturation magnetization method. Specifically, a saturation magnetization (I) of the sample and a saturation magnetization (Is) of a standard sample heated at 400° C. for 15 hours were measured and the volume percent (Vγr) of retained γ was obtained from the following Equation. The saturation magnetization was measured at the room temperature with a maximum applied magnetization set at 5000 (Oe) using an automatic direct-current magnetization B—H characteristic recording device “Model BHS-40” produced by Riken Denshi Co., Ltd.
Vγr=(1−I/1s)×100
Further, the surface of the cross-section of the sample parallel to the rolling direction was polished, Repera corrosion was caused, five view fields at the ¼ thickness position were observed at a magnification of 1000 using an optical microscope and circle-equivalent diameters d of MA mixed phases in which retained γ and tempered martensite were compounded were measured. A ratio of the number of the MA mixed phases whose circle-equivalent diameters are larger than 7 μm in the observed cross-section to the total number of the MA mixed phases was calculated. An evaluation result is shown in a column of “Evaluation Result on MA Mixed Phase Number Ratio” of Table 3 below with a case where the number ratio is 0% or higher and below 15% as good (OK) and a case where the number ratio is not lower than 15% as not good (NG).
[IQ Distribution]
A surface of a cross-section of the sample parallel to the rolling direction was polished and an EBSD measurement (OIM system produced by TexSEM Laboratories Inc.) was conducted at 180,000 points with one step of 0.25 μm for an area of 100 μm×100 μm at a ¼ thickness position. From this measurement result, an average IQ value in each grain was obtained. Note that only crystal grains completely accommodated in the measurement area were measured and measurement points of CI<0.1 were excluded from analysis. Further, in Equations (1) and (2) below, 2% of the total number of data was excluded on each of maximum and minimum sides. A value of (IQave−IQmin)/(IQmax−IQmin) was written in “Equation (1)” and a value of (σIQ)/(IQmax−IQmin) was written in “Equation (2)” in Table 3.
(IQave−IQmin)/(IQmax−IQmin)≧0.40 (1)
(σIQ)/(IQmax−IQmin)≦0.25 (2)
<<Evaluation of Mechanical Properties>
[Tensile Strength (TS), Elongation (EL)]
Tensile strength (TS) and elongation (EL) were measured by conducting a tensile test based on JIS Z2241. A test piece used was a test piece No. 5 specified by JIS Z2201 cut out from a sample such that a direction perpendicular to the rolling direction of the sample is a longitudinal direction. A measurement result is shown in each of columns of “TS (MPa)” and “EL (%)”.
[Stretch Flange Formability (λ)]
Stretch Flange formability (λ) is evaluated by a hole expansion ratio. The hole expansion ratio (λ) was measured by conducting a hole expansion test based on the Japan Iron and Steel Federation's standard JFST 1001. A measurement result is shown in a column of “A (%)” of Table 4 below.
[Bendability (R)]
Bendability (R) was evaluated by a limit bending radius. The limit bending radius was measured by conducting a V bending test based on JIS Z2248. A test piece used was a test piece No. 1 specified by JIS Z2204, having a sheet thickness of 1.4 mm and cut out from a sample such that a direction perpendicular to the rolling direction is a longitudinal direction, i.e. a bending ridge coincides with the rolling direction. Note that the V bending test was conducted after end surfaces of the test piece in the longitudinal direction were machine-ground so as not to cause cracks.
With angles of a die and a punch set at 90°, the V bending test was conducted by changing a tip radius of the punch in increments of 0.5 mm and the tip radius of the punch capable of bending the test piece without causing cracks was obtained as the limit bending radius. A measurement result is shown in a column of “Limit Bending R (mm)” of Table 4 below. Note that the presence or absence of cracks was observed using a loupe and determined on the basis of the absence of cracks.
[Erichsen Value]
An Erichsen value was measured by conducting an Erichsen test based on JIS Z2247. A test piece used was cut out from the sample to be 90 mm×90 mm×1.4 mm (thickness). The Erichsen test was conducted using a punch having a diameter of 20 mm. A measurement result is shown in a column of “Erichsen Value (mm)” of Table 4 below. Note that, according to the Erichsen test, composite effects by both the total elongation property and local ductility of the steel sheet can be evaluated.
[Low-Temperature Toughness]
Low-temperature toughness was evaluated by a brittle fracture rate (%) when a Charpy impact test was conducted at −20° C. based on JIS Z2242. A width of a test piece was 1.4 mm equal to the sheet thickness. The test piece used was a V notch test piece cut out from the sample such that a direction perpendicular to the rolling direction of the sample is a longitudinal direction. A measurement result is shown in a column of “Low-Temperature Toughness (%)” of Table 4 below.
Since mechanical properties required for steel sheets differ depending on tensile strength (TS), elongation (EL), stretch flange formability (λ), bendability (R) and the Erichsen value were evaluated according to tensile strength (TS). Low-temperature toughness was uniformly determined to be good if the brittle fracture rate was 10% or lower in the Charpy impact test at −20° C.
An evaluation result is shown in a column of “Comprehensive Evaluation” of Table 4 below with a case where all the properties including elongation (EL), stretch flange formability (λ), bendability (R), the Erichsen value and low-temperature toughness are satisfied as good (OK) and a case where any of the properties is below a reference value as not good (NG) based on the following evaluation criteria.
[Level of 590 MPa]
Tensile strength (TS): 590 MPa or more, below 780 MPa
Elongation (EL): 34% or higher
Stretch flange formability (λ): 30% or higher
Bendability (R): 0.5 mm or less
Erichsen value: 10.8 mm or more
Low-Temperature toughness: 10% or lower
[Level of 780 MPa]
Tensile strength (TS): 780 MPa or more, below 980 MPa
Elongation (EL): 25% or higher
Stretch flange formability (λ): 30% or higher
Bendability (R): 1.0 mm or less
Erichsen value: 10.4 mm or more
Low-Temperature toughness: 10% or lower
[Level of 980 MPa]
Tensile strength (TS): 980 MPa or more, below 1180 MPa
Elongation (EL): 19% or higher
Stretch flange formability (λ): 20% or higher
Bendability (R): 3.0 mm or less
Erichsen value: 10.0 mm or more
Low-Temperature toughness: 10% or lower
[Level of 1180 MPa]
Tensile strength (TS): 1180 MPa or more, below 1270 MPa
Elongation (EL): 15% or higher
Stretch flange formability (λ): 20% or higher
Bendability (R): 4.5 mm or less
Erichsen value: 9.6 mm or more
Low-Temperature toughness: 10% or lower
Note that the present invention assumes that tensile strength (TS) is 590 MPa or more and below 1270 MP and cases where tensile strength (TS) is below 590 MPa or 1270 MPa or more are exempted even if mechanical properties are good. These are written as “-” in a column of “Remarks” of Table 4 below.
The following can be considered from the above results. Any of the examples for which OK is given in the comprehensive evaluation of Table 4 is a steel sheet satisfying the requirements specified in the present invention and satisfies reference values of elongation (EL), stretch flange formability (λ), bendability (R), the Erichsen value and low-temperature toughness determined according to each tensile strength (TS). Thus, the high-strength steel sheet of the present invention is found to be good in formability in general and excellent in low-temperature toughness.
On the other hand, any of the examples for which NG is given in the comprehensive evaluation is a steel sheet not satisfying any of the requirements specified in the present invention. The details are as follows.
No. A-3 is an example in which the soaking time was too short. In this example, the amount of retained γ was small since carbide remained in a solid solution state. Thus, elongation (EL) and the Erichsen value were deteriorated.
No. A-4 is an example in which the cooling stop temperature after soaking was high and the steel sheet was not held in the T1 temperature region. In this example, the compounding of the bainite structure was insufficient and the MA mixed phases were not refined since low-temperature region generated bainite and the like were hardly generated and martensite was hardly generated. Thus, stretch flange formability (λ) was deteriorated. Further, both IQave (Equation (1)) and σIQ (Equation (2)) were deviated from the specified ranges and low-temperature toughness was poor.
No. A-5 is an example in which step cooling was performed by holding the steel sheet at 320° C. on the low temperature side below the T2 temperature region after holding the steel sheet at 440° C. on the high temperature side above the T1 temperature region after soaking. Specifically, since the holding times in the T1 temperature region and the T2 temperature region were too short, the generation amount of low-temperature region generated bainite and the like was reduced and many coarse MA mixed phases were generated. Thus, stretch flange formability (λ) and bendability (R) were deteriorated. Further, σIQ (Equation (2)) was deviated from the specified range and low-temperature toughness was poor.
No. B-3 is an example in which the holding time (s) in the T1 temperature region was too short. In this example, low-temperature region generated bainite and the like were hardly generated and the compounding of the bainite structure was insufficient. Thus, stretch flange formability (λ) and the Erichsen value were deteriorated. Further, σIQ (Equation (2)) was deviated from the specified range and low-temperature toughness was poor.
No. B-4 is an example in which the soaking temperature was too high. In this example, since the heating temperature was too high, a sufficient amount of polygonal ferrite could not be secured, whereas the generation amount of low-temperature region generated bainite and the like increased. Thus, elongation (EL) was poor.
No. C-3 is an example in which the average cooling rate “Rapid Cooling Rate (° C./s)” during cooling up to the arbitrary cooling stop temperature T in the T1 temperature region after soaking was too slow. In this example, since polygonal ferrite and perlite were generated in a large amount during cooling, the generation amount of high-temperature region generated bainite was small. Thus, elongation (EL) and the Erichsen value were deteriorated. Further, σIQ (Equation (2)) was deviated from the specified range and low-temperature toughness was poor.
No. C-4 is an example in which the holding time in the T2 temperature region was too short. In this example, since the generation amount of high-temperature region generated bainite was small, a large amount of untransformed austenite remained and carbon condensation was insufficient, hard quenched martensite was generated in a large amount during cooling from the T2 temperature region and coarse MA mixed phases were generated. Thus, elongation (EL) and stretch flange formability (λ) were deteriorated. Further, both IQave (Equation (1)) and σIQ (Equation (2)) were deviated from the specified ranges and low-temperature toughness was poor.
In No. D-3, the soaking temperature was too low, a large amount of the worked structure remained, reverse transformation into austenite hardly progressed, the generation amount of any of high-temperature region generated bainite, low-temperature region generated bainite and the like and retained austenite was small and the predetermined metal structure could not be secured. Thus, elongation (EL) and the Erichsen value were deteriorated.
No. D-4 is an example in which the steel sheet was cooled up to 80° C. as the “cooling stop temperature (° C.)” below the T1 temperature region after soaking and continued to be held at the temperature below the T1 temperature region. In this example, the generation amount of high-temperature region generated bainite could not be secured. Thus, elongation (EL) and the Erichsen value were poor.
No. E-2 is an example in which the holding time in the T1 temperature region was too long and the holding temperature in the T2 temperature region was too low. In this example, high-temperature region generated bainite could not be secured. Thus, elongation (EL) and the Erichsen value were deteriorated.
No. H-1 is an example in which step cooling was performed by holding the steel sheet at the 380° C. on the low temperature side equivalent to the T2 temperature region after holding the steel sheet at 420° C. on the high temperature side equivalent to the T1 temperature region after soaking. In this example, since a cooling pattern different from the producing method of the present invention, in which austempering is performed to hold the steel sheet in the T2 temperature region for the predetermined time, after excessive cooling, both IQave (Equation (1)) and σIQ (Equation (2)) were deviated from the specified ranges and low-temperature toughness was poor.
No. M-2 is an example in which the holding time in the T1 temperature region was too long. In this example, the amount of high-temperature region generated bainite could not be secured and the amount of retained γ was insufficient. Thus, elongation (EL) was deteriorated.
No. M-3 is an example in which the holding temperature in the T1 temperature region was too high. In this example, since perlite was generated, the generation amount of high-temperature region generated bainite could not be secured and the generation amount of retained γ was also small. Thus, elongation (EL) and the Ericksen value were deteriorated.
No. N-1 is an example in which the amount of C was too small. In this example, the generation amount of retained γ was small. Thus, elongation (EL) and the Erichsen value were deteriorated.
No. O-1 is an example in which the amount of Si was too small. In this example, the generation amount of retained γ was small. Thus, elongation (EL) and the Erichsen value were deteriorated.
No. P-1 is an example in which the amount of Mn was too small. In this example, since quenching was not sufficiently performed, ferrite was generated during cooling, the generation of low-temperature region generated bainite and the like and high-temperature region generated bainite was suppressed, the generation amount of retained γ was small and elongation (EL) and the Erichsen value were deteriorated. Further, σIQ (Equation (2)) was deviated from the specified range and low-temperature toughness was poor.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2013-202537 | Sep 2013 | JP | national |
| 2014-071906 | Mar 2014 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2014/075494 | 9/25/2014 | WO | 00 |
