BAKE-HARDENING HOT-ROLLED STEEL SHEET WITH EXCELLENT WORKABILITY AND METHOD FOR MANUFACTURING THE SAME

- NIPPON STEEL CORPORATION

According to an exemplary embodiment of the present invention, a bake-hardening hot-rolled steel sheet with excellent workability can be provided. The exemplary steel sheet can contain, in terms of mass %, C of about 0.01 to 0.2%, Si of about 0.01 to 2%, Mn of about 0.1 to 2%, P of about 0.1% or less, S of about 0.03% or less, Al of about 0.001 to 0.1%, N of about 0.01% or less, Nb of about 0.005 to 0.05%, and as the remainder, Fe and unavoidable impurities. A microstructure of the steel sheet can be a polygonal ferrite and/or a continuous-cooled microstructure having an average particle diameter of about 2 μm to 8 μm, and the grain boundary abundance ratio of solute C and/or solute N may be about 0.28 or lower. An exemplary embodiment of the present invention can also be directed to a method for manufacturing a hot-rolled steel sheet. In this exemplary method, a slab containing aforementioned components can be heated to at least a temperature satisfying the equation of SRT (° C.)=6670/{2.26−log(% Nb)(% C)}−273. The heated slab can be subjected to a rough rolling, a finish rolling under a condition where the final temperature can be in a range of the Ar3 transformation point temperature or higher and (Ar3 transformation point temperature+100° C.) or lower to obtain a rolled steel. The rolled steel can be cooled at a cooling rate of about 80° C./sec or higher from cooling initiation down to a temperature range of about 500° C. or lower to obtain a hot rolled steel sheet; and such hot rolled steel sheet can be coiled.

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Description
TECHNICAL FIELD

The present invention relates to a bake-hardening hot-rolled steel sheet with excellent workability and a method for manufacturing the same. In detail, it relates to a steel sheet including a microstructure of polygonal ferrite and/or a continuous-cooled microstructure having an average particle diameter of 2 to 8 μm, by which not only parts requiring severe working can be readily formed, but also, even in a steel sheet having a tensile strength of 370 to 640 MPa class, a strength of press material corresponding to the design strength when a steel sheet of 540 to 780 MPa class is applied, can be obtained by strain introduction by means of pressing, and a baking finish treatment.

This application claims priority from Japanese Patent Application No. 2005-010210, filed on Jan. 18, 2005, the content of which is incorporated herein by reference.

BACKGROUND ART

Recently, in order to improve the fuel efficiency of automobiles and the like, with an object of reduction in weight, the application of light metals such as Al alloy and high strength steel sheets to automobile members is in progress. However, regardless of the advantage of high specific strength, light metals such as Al alloy are remarkably expensive compared to steels, and therefore the application thereof is limited to specific usages. Consequently, in order to promote the reduction in weight for of automobiles at a lower cost in a wider range, steel sheets need to be highly strengthened.

Since the high strengthening of materials generally involves deterioration of material properties such as the formability (workability), the key to the development of high strength steel sheets depends on how to achieve the high strengthening without deteriorating the material properties. In particular, as to the properties required for steel sheets for inner plate members, structural members, and suspension members, burring workability, ductility, fatigue resistance, and corrosion resistance and the like are important, and how to balance the high strengthening and these properties at a high level, is important.

In this manner, in order to satisfy both of the high strengthening and the various properties, in particular, formability, TRIP (Transformation Induced Plasticity) steels are disclosed in which the steel microstructure includes retained austenite, and thereby the TRIP phenomenon is developed during the formation thereof, so as to greatly improve the formability (ductility and deep drawability) (for example, refer to Patent Documents 1 and 2).

However, these techniques demonstrates, at a strength level of about 590 MPa, a total elongation of about 30% and excellent deep drawability (LDR: limiting drawing ratio) due to the occurrence of TRIP phenomenon by the retained austenite. However, in order to obtain a steel sheet having strength within the range of 370 to 540 MPa, the amounts of elements such as C, Si, and Mn, have to be inevitably reduced. If the elements such as C, Si, and Mn are reduced to realize the strength within the range of 370 to 540 MPa class, there is a problem of being unable to maintain amount of retained austenite required for obtaining the TRIP phenomenon in the microstructure at room temperature. Moreover, the above techniques do not take into consideration of the improvement of burring workability. Consequently, in the current state, it is difficult to apply high strength steel sheets having strength of 590 MPa or more class to members in which steel sheet having strength on the order of about 270 to 340 MPa class is currently used, without first improving operations and equipment used during pressing. The only realistic solution for the time being is to use steel sheet having strength of about 370 to 540 MPa class. On the other hand, requirements for reduction of gauges are recently more and more increased in order to achieve the reduction in weight for automobile bodies, and it is therefore important for reduction in weight for automobile body to maintain pressed product strength as much as possible, based on the premise of reducing gauges.

Bake-hardening (BH) steel sheet has been proposed as a way of solving these problems because it has low strength during press molding and improves the strength of pressed products as a result of introducing stress due to pressing and subsequent baking finish treatment.

It is effective to increase solute C and solute N so as to improve bake hardenability; however, increases in these solute elements present in the solid solution worsen aging deterioration at normal temperatures. Consequently, it is important to develop a technology that can allow both bake hardenability and resistance to aging deterioration at normal temperatures.

On the basis of the requirements described above, technologies are disclosed for realizing both bake hardenability and resistance to aging deterioration at normal temperatures, in which bake hardenability is improved by increasing the amount of solute N, and the diffusion of solute C and solute N at normal temperatures is inhibited by an effect of increasing grain boundary surface area caused by grain refining of crystal grains (for example, refer to Patent Documents 3 and 4).

However, refining the crystal grains gives concern of deterioration of press formability. Moreover, if suspension members and inner plate members are the subject, regardless of the needs for excellent burring workability, the burring workability is considered to be inappropriate since the microstructure is ferrite-pearlite.

Patent Document 1: Japanese Unexamined Patent Application, First Publication No. 2000-169935

Patent Document 2: Japanese Unexamined Patent Application, First Publication No. 2000-169936

Patent Document 3: Japanese Unexamined Patent Application, First Publication No. Hei 10-183301

Patent Document 4: Japanese Unexamined Patent Application, First Publication No. Hei 2000-297350

DISCLOSURE OF INVENTION Problems to be Solved by the Invention

Here, the present invention provides a bake-hardening hot-rolled steel sheet with excellent workability which has excellent workability, by which a bake-hardening amount of 50 MPa or more can be obtained stably in a strength range of 370 to 640 MPa class, and a method for manufacturing the same. That is, the present invention aims to provide a bake-hardening hot-rolled steel sheet with excellent workability including a microstructure that develops excellent workability that allows to manufacture pressed product having strength equivalent to that of pressed product manufactured by applying a 540 to 780 MPa class steel sheet as a result of the introduction of pressing stress and baking finish treatment, even when the tensile strength of the hot-rolled steel sheet is 370 to 640 MPa, and a method for manufacturing that steel sheet inexpensively and stably.

Means for Solving the Problems

The inventors of the present invention conducted extensive research so as to obtain a steel sheet having superior bake hardenability and superior corrosion resistance after coating as well as excellent workability, with the emphasis on a production process for 370 to 490 MPa-class steel sheet produced on an industrial scale using ordinary production equipment currently in use.

As a result, the inventors of the present invention newly found that, a steel sheet which contains C of 0.01 to 0.2%, Si of 0.01 to 2%, Mn of 0.1 to 2%, P of 0.1% or less, S of 0.03% or less, Al of 0.001 to 0.1%, N of 0.01% or less, Nb of 0.005 to 0.05%, and as a remainder, Fe and unavoidable impurities, in which the microstructure is a polygonal ferrite and/or a continuous-cooled microstructure having an average particle diameter of 2 μm to 8 μm, and the grain boundary abundance ratio of solute C and/or solute N is 0.28 or lower, is very effective, and have achieved the present invention.

Namely, the gist of the present invention is as described below.

(1) A bake-hardening hot-rolled steel sheet with excellent workability, includes, in terms of mass %, C of 0.01 to 0.2%, Si of 0.01 to 2%, Mn of 0.1 to 2%, P of 0.1% or less, S of 0.03% or less, Al of 0.001 to 0.1%, N of 0.01% or less, Nb of 0.005 to 0.05%, and as the remainder, Fe and unavoidable impurities, wherein the microstructure is a polygonal ferrite and/or a continuous-cooled microstructure having an average particle diameter of 2 μm to 8 μm, and the grain boundary abundance ratio of solute C and/or solute N is 0.28 or lower.

(2) A bake-hardening hot-rolled steel sheet with excellent workability according to (1), which further includes one or two or more selected from, in terms of mass %, Ti of 0.001 to 0.02%, B of 0.0002 to 0.002%, Cu of 0.2 to 1.2%, Ni of 0.1 to 0.6%, Mo of 0.05 to 1%, V of 0.02 to 0.2%, and Cr of 0.01 to 1%.

(3) A bake-hardening hot-rolled steel sheet with excellent workability according to (1), which further includes one or both of, in terms of mass %, Ca of 0.0005 to 0.005% and REM of 0.0005 to 0.02%.

(4) A bake-hardening hot-rolled steel sheet with excellent workability according to (1), which is galvanized.

(5) A method for manufacturing a bake-hardening hot-rolled steel sheet with excellent workability, includes: heating a slab containing, in terms of mass %, C of 0.01 to 0.2%, Si of 0.01 to 2%, Mn of 0.1 to 2%, P of 0.1% or less, S of 0.03% or less, Al of 0.001 to 0.1%, N of 0.01% or less, Nb of 0.005 to 0.05%, and as the remainder, Fe and unavoidable impurities, to at least a temperature satisfying the following equation (A); and then subjecting the slab to a hot rolling, wherein in the hot rolling, the heated slab is subjected to a rough rolling so as to obtain a rough rolled bar, the rough rolled bar is subjected to a finish rolling under a condition where the final temperature is in a range of Ar3 transformation point temperature or higher and (Ar3 transformation point temperature+100° C.) or lower, so as to obtain a rolled steel, and cooling the rolled steel at a cooling rate of 80° C./sec or higher from cooling initiation to a temperature range of 500° C. or lower, so as to obtain a hot rolled steel sheet, and coiling the hot rolled steel sheet.


SRT(° C.)=6670/{2.26−log(% Nb)(% C)}−273  (A)

(6) A method for manufacturing a bake-hardening hot-rolled steel sheet with excellent workability according to (5), wherein the initiation temperature of the finish rolling is set to 1000° C. or higher.

(7) A method for manufacturing a bake-hardening hot-rolled steel sheet with excellent workability according to (5), wherein the rough rolled bar and/or the rolled steel is heated during the time until the initiation of the finish rolling and/or during the finish rolling.

(8) A method for manufacturing a bake-hardening hot-rolled steel sheet with excellent workability according to (5), wherein descaling is performed during the time from completion of the rough rolling until initiation of the finish rolling.

(9) A method for manufacturing a bake-hardening hot-rolled steel sheet with excellent workability according to (5), wherein the hot-rolled steel sheet obtained by the hot rolling is immersed in a galvanizing bath so as to galvanize the surface of the hot-rolled steel sheet.

(10) A method for manufacturing a bake-hardening hot-rolled steel sheet with excellent workability according to (9), wherein an alloying treatment is performed after galvanization.

EFFECTS OF THE INVENTION

By using the bake-hardening hot-rolled steel sheet with excellent workability of the present invention, not only parts requiring severe working can be readily formed, but also a bake-hardening amount of 50 MPa or more can be obtained stably in a strength range of 370 to 640 MPa class. As a result, even when the tensile strength of the steel sheet is 370 to 640 MPa, a pressed product having strength equivalent to the design strength of pressed product manufactured by applying a 540 to 780 MPa class steel sheet can be manufactured as a result of the introduction of pressing stress and baking finish treatment. From the above, the present invention can be said to be a highly industrially valuable invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the relation between crystal grain diameter and bake-hardening amount.

FIG. 2 shows the relation between crystal grain diameter and yield ratio.

FIG. 3 shows the relation between grain boundary abundance ratio of solute C and solute N, and maximum peeling width.

 BEST MODE FOR CARRYING OUT THE INVENTION

The following provides an explanation of the results of basic research leading to the present invention.

The following experiments were performed in order to examine relations between the microstructure of steel sheets and bake hardenability, corrosion resistance after coating, or workability. Slabs having the steel components shown in Table 1 were melted to prepare steel sheets having a thickness of 2 mm produced in various production processes. The bake hardenability, the corrosion resistance after coating, the yield ratio, the microstructure, and the abundant state of solute C and/or solute N thereof were examined.

TABLE 1 (mass %) C Si Mn P S Al N Nb Nb 0.068 0.95 1.22 0.009 0.003 0.014 0.0029 0.025 added Nb not 0.065 1.01 1.20 0.011 0.003 0.015 0.0031 0.001 added

The bake hardenability was evaluated in accordance with the following procedure. No. 5 test pieces as described in JIS Z 2201 were cut out from each steel sheet. Preliminary tensile strain of 2% was applied to these test pieces, and then the test pieces were subjected to heat treatment corresponding to a baking finish treatment at 170° C. for 20 minutes, after which the tensile test was performed again. The tensile test was performed in accordance with the method of JIS Z 2241. Here, the bake-hardening amount is defined as the value obtained by subtracting a flow stress of the preliminary tensile strain of 2% from the upper yield point obtained in the repeated tensile test.

The corrosion resistance after coating was evaluated in accordance with the following procedure. Firstly, the produced steel sheets were acid-washed, and then subjected to phosphating for adhering a zinc phosphate film of 2.5 g/m2. Furthermore, electrodeposition coating of the thickness of 25 μm was performed on the top surface thereof, and then a baking finish treatment was conducted at 170° C. for 20 minutes. Then, the electrodeposition coated film was cut in for a length of 130 mm with a sharp-pointed knife until reaching the steel surface, and sprayed with 5% saline solution at 35° C. for 700 hours under a saline spray condition shown in JIS Z 2371. Then, a tape (405A-24 JIS Z 1522, manufactured by Nichiban Company, Ltd.) having a width of 24 mm was adhered over the cut part in parallel therewith, in a length of 130 mm. After this tape was peeled off, the maximum peeling width of the coated film was measured.

On the other hand, the microstructure was examined in accordance with the following method. Firstly, samples cut out from a location of ¼W or ¾W of the width (W) of the steel sheets were ground along the cross-section in the direction of rolling, and then were etched using a nital reagent. Observation was performed in the fields at ¼t of the sheet thickness (t) at 200-fold to 500-fold magnification using an optical microscope, and photographs of the metal structure were taken. Here, the volume fraction of the microstructure is defined as the area fraction in the photographs of the metal structure. The average grain diameter is defined as follows. Firstly, if the microstructure is a polygonal ferrite, the crystal grain size G was obtained by the comparison method or the cutting method described in JIS G 0552. If the microstructure is a continuous-cooled microstructure, by intentionally using the cutting method described in JIS G 0552, which is inherently used to obtain the crystal grain size of polygonal ferrite grains, the grain size number G was obtained from the measurement. Next, using the obtained crystal grain size G, the number m of the crystal grains per 1 mm2 of the cross-sectional area was obtained from the equation of m=8×2G. The average grain diameter dm obtained from this number m using the equation of dm=1/(√m), is defined as the average grain diameter of the polygonal ferrite and/or the continuous-cooled microstructure. Here, the continuous-cooled microstructure (Zw) is a microstructure that is defined as a transformation structure at an intermediate stage between a microstructure that contains polygonal ferrite and pearlite formed by a diffusion mechanism, and martensite formed by a shearing mechanism in the absence of diffusion, as described in “Recent Research on the Bainite Structure of Low Carbon Steel and its Transformation Behavior-Final Report of the Bainite Research Committee”, Bainite Research Committee, Society on Basic Research, the Iron and Steel Institute of Japan, (1994, the Iron and Steel Institute of Japan). That is, as described on sections 125 to 127 of the above reference in terms of the structure observed by optical microscopy, the continuous-cooled microstructure (Zw) is defined as a microstructure which mainly includes Bainitic ferrite (α°B), Granular bainitic ferrite (αB), and Quasi-polygonal ferrite (αq), and additionally includes small amounts of retained austenite (γr) and Martensite-austenite (MA). Regarding αq, the internal structure does not appear as a result of etching in the same manner as polygonal ferrite (PF), however it has an acicular form, and thus is clearly distinguished from PF. Here, assuming that the boundary length of the target crystal grain is taken to be lq and its equivalent circular diameter is taken to be dq, grains in which their ratio of (lq/dq) satisfies the relation of lq/dq≧3.5 are αq. The continuous-cooled microstructure (Zw) in the present invention can be defined as a microstructure including any one or two or more of α°B, αB, αq, γr, and MA, provided that the total small amount of γr and MA is 3% or less.

Next, the grain boundary abundance ratio of solute C and/or solute N is measured. The grain boundary abundance ratio of solute C and/or solute N in the present invention is defined as a value obtained by dividing the total amount of the solute C and/or the solute N present in the grain boundary, by the total amount of the solute C and/or the solute N. This value may be a value obtained by calculating the sole measurement value of the solute C or the solute N. Alternatively, a value obtained by calculating the added measurement value of the solute C and the solute N, may be also employed.

In order to measure the solute C present in the grain boundary or inside the grains, a three dimensional atom probe method was used. The measurement condition was such that the temperature of the sample location was about 70K, the probe full voltage was 10 to 15 kV, and the pulse ratio was 25%. The respective samples were measured three times respectively in each of the grain boundary and inside the grains, and the average value thereof was used as the representative value. Background noise and the like were eliminated from the measurement value. The obtained value was converted into C-excess (atm/nm2) defined as the atomic density per unit grain boundary area, and then was further converted into the total amount of grain boundary face segregation from the following equation using the grain boundary volume ratio Rb.


total amount of grain boundary face segregation=average C-excess×Rb×12 (atomic weight of C)/56 (atomic weight of Fe)

Here, Rb is a value defined from the following equation, assuming that one side of a rectangular parallelepiped grain is D and the grain boundary segregation width is W=2a (a=2 nm).


Rb={D3−(D−2a)3}/D3=3(W/D)−3(W/D)2+(W/D)3

The grain boundary abundance ratio of a solute C and/or solute N is a value obtained by dividing the total amount of grain boundary face segregation obtained by the above, by the amount of solute C obtained by the internal friction method.

Concerning the measurement results of the bake-hardening amount and the like in the above method, FIG. 1 shows the relation between average crystal grain diameter and bake-hardening amount, with respect to the presence/absence of Nb addition, and the microstructure. The bake-hardening amount and the average crystal grain diameter are strongly correlated. It was newly found that, particularly in the Nb added steel, when the crystal grain diameter was 8 μm or less, the bake-hardening amount (2% BH) became 70 MPa or more. Moreover, FIG. 2 shows the relation between average crystal grain diameter and yield ratio (YR), with respect to the presence/absence of Nb addition, and the microstructure. In the Nb added steel, when the crystal grain diameter is 2 μm or more, the yield ratio is not increased even in fine grains, and the yield ratio is 70% or less. Consequently, workability such as uniform elongation is excellent. FIG. 3 shows the relation between grain boundary abundance ratio of solute C and/or solute N, and maximum peeling width. When the grain boundary abundance ratio is 0.28 or lower, the maximum peeling width is improved to 4 mm or less.

This mechanism is not completely understood; however, Nb addition provides a dragging effect in a solid state of Nb and/or a pinning effect as carbonitride precipitates, thereby suppressing recovery/recrystallization and grain growth of austenite during rolling or after rolling, delaying the 7% transformation, and decreasing the transformation temperature. It is considered that the above result was obtained because the decrease in transformation temperature has an effect of increasing the supersaturation of the solute C and the solute N which are effective for increasing the bake-hardening amount. Furthermore, Nb has an effect of refining crystal grains after transformation. Generally, since refining of crystal grains increases the yield strength, the yield ratio tends to be increased and uniform elongation tends to be decreased. Particularly, if the grain diameter is less than 5 μm, this tendency becomes remarkable; however, it is considered that Nb addition has an effect of making it easy to obtain the continuous-cooled microstructure, and suppressing the increase in yield ratio by introducing a large amount of transformation dislocation, even if the crystal grain diameter is less than 5 μm. However, if the grain diameter is less than 2 μm, the effect disappears. Moreover, if C, N, and the like are segregated too much in the grain boundary, a local battery is formed due to microscopic nonuniformity of the composition, the dissolution of the Fe ion is promoted, and thus the corrosion resistance is deteriorated. Therefore, it is considered that the corrosion resistance gets worse if the grain boundary abundance ratio of these atoms exceeds 0.28.

In the present invention, it should be noted that not only the bake-hardening amount at 2% preliminary strain evaluated in the above is excellent, but also the bake-hardening amount at 10% preliminary strain is 30 MPa or more even with N≦0.01%, and 30 MPa or more of amount of increase in tensile strength (ΔTS) at 10% preliminary strain can be obtained.

Next is an explanation of the reason for limiting the chemical components of the present invention. Hereunder, unit % showing the content of chemical components is mass %.

C is one of the most important elements in the present invention. If the content of C is more than 0.2%, not only the amount of carbides acting as origins of burring cracks increases, resulting in deterioration of the hole expanding ratio, but also the strength ends up increasing, resulting in deterioration of workability. Consequently, the content of C is set to 0.2% or less. It is preferably less than 0.1% in consideration of ductility. Moreover, if the content of C is less than 0.01%, sufficient solute C that is important for bake-hardening is not obtained, resulting in concern of a decrease in the bake-hardening amount. Therefore, it is set to 0.01% or more.

Since Si has the effect of inhibiting the precipitation of iron carbides that act as origins of burring cracks during cooling, Si is added at a content of 0.01% or more. However, the effect is saturated when added at a content of more than 2%. Consequently, the upper limit is set to 2%. Furthermore, if the content of Si is more than 1%, there is concern of generation of a tiger stripe scale pattern, which disfigures the aesthetic appearance of the surface and also the phosphating property is deteriorated. Therefore, the upper limit of the content of Si is preferably 1%.

Mn has an effect of expanding the temperature range of the austenite region towards lower temperatures, and making it easy to obtain the continuous-cooled microstructure serving as one of the constituent features of the microstructure in the present invention, during cooling after completion of rolling. Therefore, Mn is added at a content of 0.1% or more. However, since the effect of Mn is saturated when added at a content of more than 2%, the upper limit is set to 2%. Moreover, if elements other than Mn that inhibit the occurrence of hot cracks due to S are not adequately added, Mn is preferably added at a content that satisfies Mn/S≧20, in mass %. Furthermore, if Mn is added at a content that satisfies Si+Mn of more than 3%, the strength becomes excessively high, and this causes deterioration of workability. Therefore, the upper limit of the content of Mn is preferably 3%.

P is an impurity and its content is preferably as low as possible. If the content of P is more than 0.1%, workability and weldability are negatively affected. Therefore, the content of P is set to 0.1% or less. However, it is preferably 0.02% or less in consideration of the hole expanding ratio and weldability.

S generates A type inclusions that deteriorate the hole expanding ratio if an excessively large amount of S is present as well as S causes cracking during hot-rolling. Therefore, the content of S should be as low as possible. The allowable range is 0.03% or less. However, if a certain degree of hole expanding ratio is required, it is preferably 0.01% or less. Furthermore, if a higher degree of hole expansion is in demand, it is more preferably 0.003% or less.

Al should be added at a content of 0.001% or more for the purpose of deoxidation of molten steel. However, since Al leads to increase in cost, the upper limit is set to 0.1%. Moreover, since Al causes an increase in the amount of non-metallic inclusions resulting in deterioration of elongation if an excessively large amount of Al is added, it is preferably 0.06% or less. Furthermore, the content of Al is preferably 0.015% or less in order to increase the bake-hardening amount. If the coiling temperature is 350° C. or more, there is concern of promoting the precipitation of AlN which fixes the solute N that is important for bake-hardening, and invalidates it. Therefore, the content of Al is preferably 0.005% or less in order to ensure the bake-hardening amount.

N is typically a preferable element for increasing the bake-hardening amount. However, since the effect is saturated if N is added at a content of more than 0.01%, the upper limit is set to 0.01%. However, in the case where the product is applied to parts for which aging deterioration presents a problem, since aging deterioration becomes considerable if N is added at a content of more than 0.006%, the content of N is preferably 0.006% or less. Furthermore, if the precondition is such that the product is left for two weeks or more at room temperature after the production and is then subjected to working, the content of N is preferably 0.005% or less from the viewpoint of aging resistance. Moreover, the content of N is more preferably less than 0.003%, taking into consideration the case where the product is left at high temperatures during the summer or where the product is exported across the equator during transport by a marine vessel.

Nb is the most important element in the present invention. Nb provides a dragging effect in a solid state and/or a pinning effect as carbonitride precipitates, thereby suppressing the recovery/recrystallization and grain growth of austenite during rolling or after rolling, delaying the γ/α transformation, and decreasing the transformation temperature, and provides an effect of refining crystal grains after transformation. The decrease in transformation temperature has an effect of increasing the supersaturation of the solute C and the solute N which are effective for increasing the bake-hardening amount. Furthermore, refining of crystal grains increases workability in a polygonal ferrite and/or a continuous-cooled microstructure which are generated when cooling is performed at a cooling rate at which pearlite texture is not generated. However, in order to obtain these effects, Nb should be added at a content of 0.005% or more, and preferably more than 0.01%. On the other hand, the effects are saturated if Nb is added at a content of more than 0.05%, and even worse there is concern of forming carbonitride, to decrease the solute C and the solute N which are effective for increasing the bake-hardening amount.

Ti has an effect of suppressing nucleation of ferrite in γ/α transformation, and promoting the generation of a continuous-cooled microstructure. Therefore, Ti is added as required. However, in order to obtain this effect, Ti should be added at least at a content of 0.001% or more, and preferably 0.005% or more. On the other hand, the upper limit of Ti is set to 0.02%, since there is concern of forming carbonitride, to decrease the solute C and the solute N which are effective for increasing the bake-hardening amount.

B has an effect of improving quench hardenability, and making it easy to obtain the continuous-cooled microstructure. Therefore, B is added as required. However, if the content of B is less than 0.0002%, it is inadequate for obtaining that effect, whereas if the content of B is more than 0.002%, slab cracks occur. Accordingly, the content of B is set to 0.0002% or more and 0.002% or less.

Furthermore, for the purpose of imparting strength, any one or two or more of elements of Cu, Ni, Mo, V, or Cr for strengthening the precipitation or solid solution, may be added. However, if Cu is less than 0.2%, Ni is less than 0.1%, Mo is less than 0.05%, V is less than 0.02%, and Cr is less than 0.01%, the effect may not be obtained. Moreover, if Cu is more than 1.2%, Ni is more than 0.6%, Mo is more than 1%, V is more than 0.2%, and Cr is more than 1%, the effect is saturated.

Ca and REM are elements which change the forms of non-metallic inclusions acting as origins of breakage and causing deterioration of workability, and then eliminate their harmful effects. However, they are not effective if added at contents of less than 0.0005%, while their effects are saturated if Ca is added at a content of more than 0.005% or REM is added at a content of more than 0.02%. Consequently, Ca is preferably added at a content of 0.0005 to 0.005%, and REM is preferably added at a content of 0.0005 to 0.02%. Here, REM stands for rare earth metal element, and is one or more selected from Sc, Y, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.

The steel having these as the main components may further contain Ti, Nb, Zr, Sn, Co, Zn, W or Mg at a total content of 1% or less. However, since with Sn there is concern of causing imperfections during hot-rolling, the content of Sn is preferably 0.05% or less.

Next, the following provides a detailed description of the microstructure of the steel sheet in the present invention.

In order to satisfy all of the bake hardenability, the corrosion resistance after coating, and the workability, the microstructure has to be a polygonal ferrite and/or a continuous-cooled microstructure which have an average particle diameter of 2 μm to 8 μm, and the grain boundary abundance ratio of solute C and/or solute N has to be 0.28 or lower. Here, the continuous-cooled microstructure (Zw) in the present invention is a microstructure including one or two or more of α°B, αB, αq, γr, and MA, provided that the total small amount of γr and MA is 3% or less. As described above, in order to satisfy both of excellent bake hardenability and excellent workability, the continuous-cooled microstructure is better; however, similar effects can be obtained with a polygonal ferrite having an average grain diameter of 8 μm or less as a microstructure of the steel sheet, as well as the continuous-cooled microstructure.

Next, the following provides a detailed description of the reason for limiting the production process of the present invention.

The hot-rolled steel sheet of the present invention includes: hot-rolled steel sheets which are after casting, cooled down after hot-rolling; hot-rolled steel sheets after hot-rolling; hot-rolled steel sheets applied with a heat treatment on a hot-dip coating line; and hot-rolled steel sheets obtained by applying these hot-rolled steel sheets with a surface treatment.

In the present invention, the production process preceding hot-rolling is not specifically limited. That is, melting is performed in a blast furnace, a converter, an electric furnace, or the like, and then quality governing is conducted in a variety of secondary refining so as to achieve the target contents of the components. Next, casting may be performed by a normal continuous casting, an ingot method, as well as a method such as thin slab casting. Scraps may be used for the raw material. In the case of a slab (steel billet) obtained by continuous casting, it may be either sent directly to a hot-rolling machine as a high temperature cast steel, or cooled down to room temperature and then reheated in a heating furnace, and then hot-rolled.

When the slab is hot-rolled, firstly the slab is heated. The slab reheating temperature (SRT) at this time is set to at least a temperature calculated by the following equation (A).


SRT(° C.)=6670/{2.26−log(% Nb)(% C)}−273  (A)

Here, % Nb and % C in the equation denote the contents (mass %) of respective elements Nb and C in the slab.

If the reheating temperature is lower than the above temperature, Nb carbonitrides are not adequately dissolved, and therefore effects of Nb such as suppressing the recovery/recrystallization and grain growth of austenite in the following rolling step, and refining crystal grains by delaying the γ/α transformation, can not be obtained. Consequently, the slab reheating temperature (SRT) is set to at least a temperature calculated by the above equation. However, if the temperature is 1400° C. or higher, the amount of scale-off becomes excessive, resulting in a decrease in yield. Therefore, the reheating temperature is preferably lower than 1400° C. Moreover, if heating is performed at a temperature of lower than 1000° C., operating efficiency is considerably impaired in terms of scheduling. Therefore, the slab reheating temperature is preferably 1000° C. or higher. Furthermore, if heating is performed at a temperature of lower than 1100° C., the amount of scale-off becomes small, causing a possibility that inclusions in the surface layer of the slab can not be removed together with the scales by subsequent descaling. Therefore, the slab reheating temperature is preferably 1100° C. or higher. The slab heating time is not specifically specified; however, in order to sufficiently promote dissolution of Nb carbonitrides, it is desirable to hold for 30 minutes or more after reaching that temperature. However, if the cast steel after casting is directly sent at a high temperature to be rolled, the time is not limited to the above.

Next, hot-rolling is performed. In the hot-rolling step, firstly, the heated slab is rough-rolled to make a rough rolled bar. In this rough-rolling, for example, the slab is rolled into a thickness of about 80 mm or less, so that the rough rolled bar can be gripped in the roll of the finish-rolling machine. Then, the rough rolled bar is subjected to finish rolling to make a rolled steel. In order to obtain a more uniform continuous-cooled microstructure in the thickness direction, the initiation temperature of finish rolling is set to 1000° C. or higher, and more preferably to 1050° C. or higher. To achieve this, the rough rolled bar or the rolled steel is preferably heated during the time from the completion of the rough rolling until the initiation of the finish rolling, and/or during the finish rolling, as required.

In particular, in order to stably obtain excellent total elongation in the present invention, it is effective to inhibit the fine precipitation of MnS and so forth. The heating device in this case may be any type; however, a transverse type is preferable since the transverse type can heat uniformly in the thickness direction. Normally, precipitates such as MnS are redissolved in a solid solution during reheating of the slab at about 1250° C., and finely precipitate during the subsequent hot rolling. Consequently, ductility can be improved by controlling the slab reheating temperature to about 1150° C. so as to prevent MnS from being redissolved in a solid solution. However, in order to set the final temperature of rolling within the range of the present invention, it is an effective means to heat the rough rolled bar or the rolled steel during the time from completion of rough rolling until initiation of finish rolling, and/or during the finish rolling.

Descaling may be performed during the time from the completion of the rough rolling until the initiation of the finish rolling. In this case, collision pressure P (MPa) and flow rate L (liters/cm2) of high-pressure water on the surface of the steel sheet satisfy the conditional equation of P (MPa)×flow rate L (liters/cm2)≧0.0025.

The collision pressure P of the high-pressure water on the surface of the steel sheet is described in the following manner (refer to “Iron and Steel”, 1991, Vol. 77, No. 9, p. 1450).


P(MPa)=5.64×P0×V/H2

where, P0 (MPa): Liquid pressure,

V (liters/min): Flow rate of liquid from nozzle, and

H (cm): Distance between surface of steel sheet and nozzle.

The flow rate L is described in the following manner.


L(liters/cm2)=V/(W×v)

where, V (liters/min): Flow rate of liquid from nozzle,

W (cm): Width of spraying liquid that contacts the surface of the steel sheet per nozzle, and

v (cm/min): Sheet transport speed.

It is not particularly necessary to specify the upper limit of value of collision pressure P×flow rate L in order to obtain the effects of the present invention. However, it is preferably set to 0.02 or less, since excessive nozzle wear and other problems occur when the nozzle liquid flow rate is increased.

Furthermore, the maximum height Ry of the finish-rolled steel sheet surface is preferably 15 μm (15 μm Ry, 12.5 mm, ln 12.5 mm) or less. This is apparent, as described, for example, on page 84 of the Metal Material Fatigue Design Handbook, Society of Materials Science, Japan, from the fact that the fatigue strength of hot-rolled or acid-washed steel sheet is correlated with the maximum height Ry of the steel sheet surface. Moreover, the subsequent finish rolling is preferably performed within 5 seconds after the descaling so as to prevent reformation of scale.

Furthermore, sheet bars may be joined between the rough rolling and the finish rolling, and the finish rolling may be continuously performed. At that time, the rough rolled bar may be temporarily coiling into the shape of a coil, put in a cover having a warming function if necessary, and then joined after uncoiling.

The finish rolling is performed under a condition where the final temperature (FT) of the finish rolling is in a range of Ar3 transformation point temperature or higher and (Ar3 transformation point temperature+100° C.) or lower. Here, the Ar3 transformation point temperature is simply shown by, for example, the relation with the steel components in accordance with the following calculation equations.


Ar3=910−310×% C+25×% Si−80×% Mneq

where, Mneq=% Mn+% Cr+% Cu+% Mo+% Ni/2+10(% Nb−0.02).

Or, in the case of including B, Mneq=% Mn+% Cr+% Cu+% Mo+% Ni/2+10(% Nb−0.02)+1.

Here, the parameters of % C, % Si, % Mn, % Cr, % Cu, % Mo, % Ni, and % Nb in the equations indicate the respective contents (mass %) of elements C, Si, Mn, Cr, Cu, Mo, Ni and Nb in the slabs.

If the final temperature (FT) of the finish rolling is lower than the Ar3 transformation point temperature, there is a possibility of α+γ two phase region rolling; thereby, worked structure remains in the rolled ferrite grains, resulting in the risk of deterioration of ductility, and the crystal grain diameter becomes less than 2 μm, leading to concern of increasing the yield ratio. Accordingly, the final temperature is set to the Ar3 transformation point temperature or higher. On the other hand, if the final temperature is higher than (Ar3 transformation point temperature +100° C.), a dragging effect and/or a pinning effect for suppressing the recovery/recrystallization and grain growth of austenite by Nb addition, disappear, and thus it becomes difficult to obtain a crystal grain diameter of 8 μm or less, causing concern of decreasing the bake-hardening amount. Whether or not the roll pass schedule in the respective stands in the finish rolling is specifically limited, the effects of the present invention can be obtained. However, from the viewpoint of accuracy of the sheet shape, the rolling rate at the final stand is preferably lower than 10%.

After the completion of finish rolling, the steel sheet is cooled at an average cooling rate of 80° C./sec or higher to a temperature range of 500° C. or lower, to make a hot-rolled steel sheet. The initiation temperature of cooling is not specifically limited. If the cooling is initiated at a temperature of the Ar3 transformation point temperature or higher, the microstructure mainly becomes a continuous-cooled microstructure. If the cooling is initiated at a temperature below the Ar3 transformation point temperature, the microstructure contains a polygonal ferrite therein.

In any case, if the cooling rate is less than the above, there is concern that the crystal grains grow and an average particle diameter of 8 μm or less can not be obtained. The effects of the present invention seem to be obtainable without particularly specifying the upper limit of the cooling rate. However, if it is higher than 500° C./sec, the crystal grain diameter becomes less than 2 μm, causing concern of increasing the yield ratio. Thus, the cooling rate is preferably 500° C./sec or lower. Furthermore, since there is concern of warp in the sheet due to thermal strain, it is preferably set 250° C./sec or lower. Moreover, a uniform microstructure is desirable in order to improve the burring workability. In order to obtain such a microstructure, the cooling rate is preferably 130° C./sec or higher.

If the cooling is stopped at a temperature higher than 500° C., there is concern of generation of a phase containing bulky carbides such as pearlite, that is unpreferable for workability. Therefore, the cooling is performed to a temperature range of 500° C. or lower. However, unless the cooling is initiated within 5 seconds after completion of finish rolling, recrystallization and grain growth of austenite progress, and thus it becomes difficult to obtain a crystal grain diameter of 8 μm or less, causing concern of decreasing the bake-hardening amount. Accordingly, it is desirable to start cooling within 5 seconds after completion of finish rolling.

After completion of the cooling, coiling is performed. If the coiling temperature is higher than 500° C., C and/or N are easily diffused, and solute C and/or solute N that increase the bake hardenability can not be sufficiently ensured. Therefore, the coiling temperature is set to 500° C. or lower. In order to increase the bake hardenability, it is preferably 450° C. or lower. Moreover, in order to obtain the bake-hardening amount of 80 MPa or more, and to suppress the generation of yield point elongation stably at all times, the coiling temperature is more preferably 350° C. or lower. Furthermore, from the viewpoint of resistance to aging deterioration, it is even more preferably 150° C. or lower. It is not necessary to specifically limit the lower limit of the coiling temperature. However, due to concern of defective appearance caused by rust if the coil is wet for a long time, the most desirable temperature is 50° C. or higher.

After completion of the hot rolling step, acid washing may be performed if necessary, and then skinpass at a reduction rate of 10% or less, or cold rolling at a reduction rate of up to about 40% may be performed either offline or inline.

Skinpass rolling is preferably performed at 0.1% or more and 0.2% or less so as to correct the shape of the steel sheet and to improve ductility due to introduction of mobile dislocations.

In order to galvanize the hot rolled steel sheet after acid washing, the hot rolled steel sheet may be immersed in a galvanizing bath, and if necessary, subjected to alloying treatment.

EXAMPLES

The following provides a more detailed explanation of the present invention through its examples.

Steels A to K having the chemical components shown in Table 2 were melted using a converter and were subjected to continuous casting. Then, they were either sent directly to rough rolling, or reheated prior to rough rolling and were subjected to rough rolling, and finish rolling so as to make the sheet thickness 1.2 to 5.5 mm, and were coiled. The chemical compositions shown in the table are indicated in mass %. Moreover, regarding the steel D, after rough rolling, descaling was performed under a condition where the collision pressure was 2.7 MPa and the flow rate was 0.001 liters/cm2. Furthermore, as shown in Table 4, the steel I was galvanized.

TABLE 2 Chemical composition (unit: mass %) Steel C Si Mn P S Al N Nb Others A 0.068 0.95 1.22 0.009 0.003 0.014 0.0029 0.025 B 0.065 1.01 1.20 0.011 0.003 0.015 0.0031 0.001 C 0.150 0.02 1.10 0.012 0.001 0.030 0.0044 0.012 Ti: 0.02% D 0.091 0.22 0.82 0.010 0.001 0.033 0.0038 0.011 Cu: 0.29%, Ni: 0.11% E 0.031 0.71 1.95 0.011 0.001 0.028 0.0050 0.027 Cr: 0.08% F 0.006 0.61 0.43 0.087 0.001 0.019 0.0019 0.015 Ti: 0.055% G 0.056 0.17 1.93 0.009 0.001 0.062 0.0020 0.031 Mo: 0.12% H 0.072 0.05 1.31 0.009 0.001 0.016 0.0030 0.030 V: 0.098% I 0.052 1.02 1.76 0.010 0.001 0.005 0.0036 0.010 B: 0.0003%, REM: 0.0008% J 0.210 1.45 1.51 0.007 0.001 0.032 0.0048 0.021 K 0.058 0.89 1.72 0.010 0.001 0.051 0.0061 0.045 Ca: 0.0015%

The details of the production conditions are shown in Table 3 and Table 4. Here, “heating rough rolled bar” indicates heating of the rough rolled bar or the rolled steel during the time from completion of rough rolling until initiation of finish rolling and/or during the finish rolling, and indicates whether or not this heating has been carried out “FT0” indicates the initiation temperature of finish rolling. “FT” indicates the final temperature of finish rolling. “Time until cooling initiation” indicates the time from completion of finish rolling until cooling is initiated. “Cooling rate down to 500° C.” indicates the average cooling rate when the rolled steels were cooled in the temperature range from the initiation temperature of cooling down to 500° C. “CT” indicates the coiling temperature.

In the tensile test of the thin steel sheets obtained in this manner, firstly the sample materials were worked into No. 5 test pieces as described in JIS Z 2201, and then subjected to the test in accordance with the method described in JIS Z 2241. In the tables, “YP” indicates the yield point, “TS” indicates the tensile strength, “EI” indicates the elongation, and “YR” indicates the yield ratio.

The BH test was performed similarly to the tensile test, in which the steel sheets were worked into No. 5 test pieces as described in JIS Z 2201, preliminary tensile strain of 2% was applied to the test pieces, thereafter heat treatment corresponding to a baking finish treatment at 170° C. for 20 minutes, and then the tensile test was performed again. Here, the bake-hardening amount (2% BH) is defined as the value obtained by subtracting a flow stress of the preliminary tensile strain of 2% from the upper yield point obtained in the repeated tensile test.

The corrosion resistance after coating was evaluated in accordance with the following procedure. Firstly, the produced steel sheets were acid-washed, and then subjected to phosphating for adhering a zinc phosphate film of 2.5 g/m2. Furthermore, electrodeposition coating was performed to a thickness of 25 μm on the top surface thereof, and then baking finish treatment was conducted at 170° C. for 20 minutes. Then, the electrodeposition coated film was cut in for a length of 130 mm with a sharp-pointed knife until reaching the steel surface, and sprayed with 5% saline solution at 35° C. for 700 hours under a saline spray condition shown in JIS Z 2371. Then, a tape (405A-24 JIS Z 1522, manufactured by Nichiban Company, Ltd.) having a width of 24 mm was adhered over the cut part in parallel therewith, in a length of 130 mm. After this tape was peeled off, the maximum peeling width of the coated film was measured.

On the other hand, the microstructure was examined in accordance with the following method. Firstly, samples cut out from a location of ¼W or ¾W of the width (W) of the steel sheets were ground along the cross-section in the direction of rolling, and were then etched using a nital reagent. Observation was performed in the fields at ¼t of the sheet thickness (t) at 200-fold to 500-fold magnification using an optical microscope, and photographs of metal structure were taken. Here, volume fraction of the microstructure is defined as the area fraction in the photographs of metal structure. Next, the average grain diameter of continuous-cooled microstructure is defined as follows. Firstly, intentionally using the cutting method described in JIS G 0552, which is inherently used to obtain the crystal grain size of polygonal ferrite grains, the grain size number G was obtained from the measurement. Next, using the obtained grain size number G, the number m of the crystal grains per 1 mm2 of the cross-sectional area was obtained from the equation of m=8×2G. The average grain diameter dm obtained from this number m using the equation of dm=1/(√m), is defined as the average grain diameter of continuous-cooled microstructure. Here, the continuous-cooled microstructure (Zw) is a microstructure that is defined as a transformation structure at an intermediate stage between a polygonal ferrite formed by a diffusion mechanism, and martensite in the absence of diffusion, as described in “Recent Research on the Bainite Structure of Low Carbon Steel and its Transformation Behavior-Final Report of the Bainite Research Committee”, Bainite Research Committee, Society on Basic Research, the Iron and Steel Institute of Japan, (1994, the Iron and Steel Institute of Japan). That is, as described in sections 125 to 127 of the above reference in terms of the structure observed by optical microscopy, the continuous-cooled microstructure (Zw) is defined as a microstructure which mainly includes Bainitic ferrite (α°B), Granular bainitic ferrite (αB), and Quasi-polygonal ferrite (αq), and additionally includes small amounts of retained austenite (γr) and Martensite-austenite (MA). Regarding the αq, the internal structure does not appear as a result of etching in the same manner as PF, however it has an acicular form, and thus is clearly distinguished from PF. Here, assuming that the boundary length of the target crystal grain is taken to be lq and its equivalent circular diameter is taken to be dq, grains in which their ratio of (lq/dq) satisfies the relation of lq/dq≧3.5 are aq. The continuous-cooled microstructure (Zw) in the present invention can be defined as a microstructure including any one or two or more of α°B, αB, αq, γr, and MA, provided that the total small amount of γr and MA is 3% or less.

Grain boundary abundance ratio of solute C and/or solute N was measured. The grain boundary abundance ratio of solute C and/or solute N in the present invention is defined as a value obtained by dividing the total amount of the solute C and/or the solute N present in the grain boundary, by the total amount of the solute C and/or the solute N. This value may be a value obtained by calculating the sole measurement value of the solute C or the solute N. Alternatively, a value obtained by calculating the added measurement value of the solute C and the solute N, may be also employed.

In order to measure the solute C present in the grain boundary or inside the grains, a three dimensional atom probe method was used. The measurement condition was such that the temperature of the sample location was about 70K, the probe full voltage was 10 to 15 kV, and the pulse ratio was 25%. The respective samples were measured three times respectively in each of the grain boundary and inside the grains, and the average value thereof was used as the representative value. Background noise and the like were eliminated from the measurement value. The obtained value was converted into C-excess (atm/nm2) defined as the atomic density per unit grain boundary area, and then was further converted into the total amount of grain boundary face segregation from the following equation using the grain boundary volume ratio Rb.


the total amount of grain boundary face segregation=average C-excess×Rb×12 (atomic weight of C)/56 (atomic weight of Fe)

Here, Rb was a value defined from the following equation, assuming that one side of a rectangular parallelepiped grain is D and the grain boundary segregation width is W=2a(a=2 nm).


Rb={D3−(D−2a)3}/D3=3(W/D)−3(W/D)2+(W/D)3

The grain boundary abundance ratio of solute C and/or solute N is a value obtained by dividing the total amount of grain boundary face segregation obtained by the above, by the amount of solute C obtained by the internal friction method.

13 steels out of steels A-2, A-3, A-4, A-5, A-6, A-7, C, D, E, G, H, I, and K satisfy the range of the present invention. All of these steels are a bake-hardening hot-rolled steel sheet with excellent workability which contains predetermined amounts of steel components, in which the microstructure is a polygonal ferrite and/or a continuous-cooled microstructure having an average particle diameter of 2 to 8 μm, and the grain boundary abundance ratio of solute C and/or solute N is 0.28 or lower. Consequently, the bake-hardening amount (2% BH), the corrosion resistance, and the yield ratio (YR) evaluated by the method described in the present invention satisfy 70 MPa or more, 4.0 mm or less, and 70% or less, respectively.

Other steels than the above are out of the range of the present invention because of the following reasons. That is, in the steel A-1, since the cooling rate down to 500° C. is more than 500° C./sec, the microstructure serving as the object of the present invention can not be obtained, and a sufficiently low yield ratio can not be obtained. In the steel A-8, since the time until cooling initiation is 5 seconds or more, the microstructure serving as the object of the present invention can not be obtained, and a sufficient bake-hardening amount can not be obtained. In the steel A-9, since the final temperature of finish rolling (FT) is lower than the Ar3 transformation point temperature, the microstructure serving as the object of the present invention can not be obtained, and a sufficiently low yield ratio can not be obtained. In the steel B, since the Nb content is out of the range of 0.005 to 0.05 mass % (less than 0.005 mass %), a sufficient bake-hardening amount can not be obtained. In the steel F, since the C content is out of the range of 0.01 to 0.2 mass % (less than 0.01 mass %), and the microstructure serving as the object of the present invention can not be obtained, a sufficient bake-hardening amount can not be obtained. In the steel J, since the C content is out of the range of 0.01 to 0.2 mass % (more than 0.2 mass %), a sufficient bake-hardening amount can not be obtained.

TABLE 3 Production condition Time until Cooling Heating lower Heating cooling Cooling rate to Steel limit target temp. actual Heating FT0 FT Ar3 Ar3 + 100 initiation initiation 500° C. CT No. (° C.) (° C.) rough bar (° C.) (° C.) (° C.) (° C.) (sec) temp. (° C.) (° C./sec) (° C.) A-1 1073 1200 Performed 1050 900 811 911 1.0 885 520 <150 A-2 1073 1200 Performed 1050 900 811 911 1.0 885 120 <150 A-3 1073 1200 Performed 1050 840 811 911 1.0 825 120 <150 A-4 1073 1200 Performed 1050 840 811 911 4.0 780 120 <150 A-5 1073 1200 Performed 1050 840 811 911 4.0 780  80 <150 A-6 1073 1200 Performed 1050 840 811 911 4.0 780  80   450 A-7 1073 1200 Performed 1050 840 811 911 4.0 780  80   450 A-8 1073 1200 Performed 1050 840 811 911 6.0 750  80   550 A-9 1073 1200 Performed 1050 800 811 911 4.0 740  80   450 B 777 1180 Not 1050 900 834 934 6.0 810 120 <150 performed Microstructure Corrosion Crystal Grain BH resistance grain boundary Mechanical property property Maximum Steel Micro- diameter abundance YP TS EI YR 2% BH peeling No. structure (μm) ratio (MPa) (MPa) (%) (%) (MPa) width (mm) Comments A-1 Zw 1.8 0.20 640 791 22 81 95 1.5 Comparative steel A-2 Zw 2.2 0.19 544 783 25 69 93 1.5 Present invention A-3 Zw 4.0 0.10 512 746 26 69 88 0.0 Present invention A-4 Zw + PF 6.0 0.07 495 728 27 68 85 0.0 Present invention A-5 PF + Zw 4.0 0.22 474 720 28 66 82 1.5 Present invention A-6 PF 5.0 0.26 480 733 27 65 78 2.0 Present invention A-7 PF 6.0 0.25 465 717 28 65 75 2.0 Present invention A-8 PF 9.0 0.57 446 693 29 64 57 7.5 Comparative steel A-9 Worked 7.0 0.37 690 734 11 94 63 7.0 Comparative PF steel B Zw 4.0 0.10 393 630 31 62 61 0.0 Comparative steel

TABLE 4 Production condition Time until Cooling Heating lower Heating cooling Cooling rate to Steel limit target temp. actual Heating FT0 FT Ar3 Ar3 + 100 initiation initiation 500° C. CT No. (° C.) (° C.) rough bar (° C.) (° C.) (° C.) (° C.) (sec) temp. (° C.) (° C./sec) (° C.) C 1080 1180 Not 1100 850 782 882 4.0 790  80   450 performed D (*1) 1014 1180 Not 1100 870 801 901 4.0 810  80   450 performed E 995 1180 Not 1100 800 750 850 1.0 785 120   450 performed F 801 1180 Not 1100 920 893 993 1.0 905  40   650 performed G 1075 1180 Performed 1100 820 724 824 1.0 805  80   450 H 1101 1230 Performed 1100 850 776 876 4.0 790  80   450 I (*2) 948 1230 Performed 1100 800 707 807 1.0 785 120 <150 J 1194 1230 Performed 1100 830 760 860 5.0 755  40   400 K 1125 1230 Performed 1100 850 757 857 1.0 835 120 <150 Microstructure Corrosion Crystal Grain BH resistance grain boundary Mechanical property property Maximum Steel Micro- diameter abundance YP TS EI YR 2% BH peeling No. structure (μm) ratio (MPa) (MPa) (%) (%) (MPa) width (mm) Comments C Zw 6.5 0.14 411 596 28 69 74 1.0 Present invention D (*1) PF + Zw 7.0 0.25 376 562 29 67 71 2.0 Present invention E Zw 3.5 0.26 430 621 27 69 88 2.0 Present invention F PF 25.0  0.00 290 468 39 62  0 0.0 Comparative steel G Zw + PF 7.0 0.23 570 811 23 70 70 1.5 Present invention H PF 4.0 0.27 340 498 35 68 86 2.0 Present invention I (*2) Zw 5.5 0.07 444 644 31 69 80 0.0 Present invention J PF + B + 8.5 0.30 588 844 32 70 43 7.0 Comparative γR steel K Zw 3.0 0.14 500 751 28 67 94 1.0 Present invention (*1); After rough-rolling, descaling with a collision pressure of 2.7 MPa and a flow rate of 0.001 liters/cm2 was performed. (*2); Galvanizing was performed.

INDUSTRIAL APPLICABILITY

By using the bake-hardening hot-rolled steel sheet with excellent workability of the present invention, not only parts requiring severe working can be readily formed, but also a bake-hardening amount of 50 MPa or more can be obtained stably in a strength range of 370 to 640 MPa class. Therefore, the present invention can be utilized particularly for a steel sheet for automobile parts, and a process for manufacturing the same, and can contribute to reduction in weight for automobile bodies at low cost.

Claims

1-10. (canceled)

11. A bake-hardening hot-rolled steel sheet having a particular workability, comprising:

at least one portion which comprises, in terms of mass %: C of about 0.01 to 0.2%, Si of about 0.01 to 2%, Mn of about 0.1 to 2%, P of about 0.1% or less, S of about 0.03% or less, Al of about 0.001 to 0.1%, N of about 0.01% or less, Nb of about 0.005 to 0.05%, and a remainder thereof with Fe and unavoidable impurities,
wherein the at least one portion has at least one of a polygonal ferrite microstructure or a continuous-cooled microstructure having an average particle diameter of about 2 μm to 8 μm, and
wherein the at least one portion has a grain boundary abundance ratio of at least one of solute C or solute N that is about 0.28 or lower.

12. The bake-hardening hot-rolled steel sheet according to claim 11, wherein the at least one portion comprises, in terms of mass %, at least one of:

Ti of about 0.001 to 0.02%,
B of about 0.0002 to 0.002%,
Cu of about 0.2 to 1.2%,
Ni of about 0.1 to 0.6%,
Mo of about 0.05 to 1%,
V of about 0.02 to 0.2%, or
Cr of about 0.01 to 1%.

13. The bake-hardening hot-rolled steel sheet according to claim 11, wherein the at least one portion comprises, in terms of mass %, at least one of:

Ca of about 0.0005 to 0.005%, and
REM of about 0.0005 to 0.02%.

14. The bake-hardening hot-rolled steel sheet according to claim 11, wherein the at least one portion is galvanized.

15. A method for manufacturing a bake-hardening hot-rolled steel sheet with a particular workability, comprising:

heating at least one portion of a slab containing, in terms of mass %, C of about 0.01 to 0.2%, Si of about 0.01 to 2%, Mn of about 0.1 to 2%, P of about 0.1% or less, S of about 0.03% or less, Al of about 0.001 to 0.1%, N of about 0.01% or less, Nb of about 0.005 to 0.05%, and a remainder thereof with Fe and unavoidable impurities, wherein the at least one portion is heated at least to a temperature satisfying the following equation: SRT(° C.)=6670/{2.26−log(% Nb)(% C)}−273;
hot rolling the at least one heated portion; wherein during the hot rolling, the heated slab is rough rolled so as to obtain a rough rolled bar;
finish rolling the rough rolled bar under a condition where a final temperature is in a range between approximately Ar3 transformation point temperature or higher and approximately Ar3 transformation point temperature +100° C. or lower so as to obtain a rolled steel;
cooling the rolled steel at a cooling rate of about 80° C./sec or higher from a cooling initiation temperature in the finish rolling to a temperature range of about 500° C. or lower, so as to obtain a hot rolled steel sheet; and
coiling the hot rolled steel sheet.

16. The method according to claim 15, wherein the initiation temperature of the finish rolling is set to about 1000° C. or higher.

17. The method according to claim 15, further comprising heating at least one of the rough rolled bar or the rolled steel at least one of until an initiation of the finish rolling or during the finish rolling.

18. The method according to claim 15, further comprising descaling the at least one portion from a completion of the rough rolling until an initiation of the finish rolling.

19. The method according to claim 15, further comprising immersing the hot-rolled steel sheet obtained by the hot rolling in a galvanizing bath so as to galvanize a surface of the hot-rolled steel sheet.

20. The method according to claim 19, further comprising performing an alloying treatment after a galvanization of the at least one portion.

Patent History
Publication number: 20100000633
Type: Application
Filed: Jan 12, 2006
Publication Date: Jan 7, 2010
Applicant: NIPPON STEEL CORPORATION (Chiyoda-ku, Tokyo)
Inventors: Tatsuo Yokoi (Oita-shi), Tetsuya Yamada (Oita-ken), Fuminori Tasaki (Oita-ken)
Application Number: 11/722,466
Classifications
Current U.S. Class: With Working Step (148/504); Ferrous (i.e., Iron Base) (148/320); Beryllium Or Boron Containing (148/330); Copper Containing (148/332); Chromium Containing, But Less Than 9 Percent (148/333); Rare Earth Meal Containing (148/331)
International Classification: C21D 11/00 (20060101); C22C 38/16 (20060101); C22C 38/18 (20060101); C22C 38/00 (20060101); C21D 9/46 (20060101);