JPH09143570A - Production of high tensile strength steel plate having extremely fine structure - Google Patents

Production of high tensile strength steel plate having extremely fine structure

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Publication number
JPH09143570A
JPH09143570A JP30026295A JP30026295A JPH09143570A JP H09143570 A JPH09143570 A JP H09143570A JP 30026295 A JP30026295 A JP 30026295A JP 30026295 A JP30026295 A JP 30026295A JP H09143570 A JPH09143570 A JP H09143570A
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JP
Japan
Prior art keywords
less
temperature
ferrite
rolling
sec
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP30026295A
Other languages
Japanese (ja)
Other versions
JP3477955B2 (en
Inventor
Masahiko Morita
正彦 森田
Susumu Okada
岡田  進
Yoshio Yamazaki
義男 山崎
Takashi Kobayashi
崇 小林
Toshiyuki Kato
俊之 加藤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Steel Corp
Original Assignee
Kawasaki Steel Corp
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Filing date
Publication date
Application filed by Kawasaki Steel Corp filed Critical Kawasaki Steel Corp
Priority to JP30026295A priority Critical patent/JP3477955B2/en
Publication of JPH09143570A publication Critical patent/JPH09143570A/en
Application granted granted Critical
Publication of JP3477955B2 publication Critical patent/JP3477955B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Heat Treatment Of Sheet Steel (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a method for producing a high tensil strength hot rolled steel plate extremely excellent in ductility, toughness and fatigue strength. SOLUTION: A steel contg., by weight, 0.05 to 0.30% C, <=2.0% Si, 1.0 to 2.5% Mn and <=0.05% Al and contg. one or two kinds of 0.05 to 0.3% Ti and <=0.10% Nb, and the balance Fe with inevitable impurities is heated at 950 to 1100 deg.C, is thereafter applied with rolling reduction so as to regulated the draft to >=20% for at least >= two times and is subjected to hot rolling so as to regulate the finishing temp. to the Ar3 transformation point or above. After that, it is cooled in the temp. range of the Ar3 transformation point or above to 750 deg.C at a rate of >=20C/sec, is successively retained in the temp. range of <750 to 600 deg.C for 5 to 20sec, is again cooled to <=550 deg.C at a rate of >=20C/sec and is coiled round a coil at <=550 deg.C to obtain an extremely fine structure in which the ferrite volume rate is regulated to >=80% and the average ferrite grain size to <10μm.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】この発明は、自動車用材、構
造材、パイプ材等の用途に用いて好適な高張力熱延鋼板
の製造方法に関し、とくに熱延ままで極微細なフェライ
ト粒を有し、延性、靱性、疲労強度に優れる高張力熱延
鋼板の製造方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a high-strength hot-rolled steel sheet suitable for use in automobile materials, structural materials, pipe materials, etc., and particularly, it has ultrafine ferrite grains as hot-rolled. , A high-strength hot-rolled steel sheet having excellent ductility, toughness, and fatigue strength.

【0002】[0002]

【従来の技術】自動車用材、構造材、パイプ材などに用
いられる鋼材の機械的性質を向上させるためには、一般
に、金属組織を微細化することが有効であり、極微細組
織を目指す製造方法が従来より数多く模索されてきた。
特に近年では、低コスト化のために高張力鋼板が多く使
用されるようになり、高張力化に伴う延性、靭性、耐久
比などの劣化を抑える目的で高張力鋼における組織の微
細化が重要な課題となっている。
2. Description of the Related Art In order to improve the mechanical properties of steel materials used for automobile materials, structural materials, pipe materials, etc., it is generally effective to refine the metal structure, and a manufacturing method aiming at an ultrafine structure. Has been sought after a lot.
Particularly in recent years, high-strength steel sheets have been widely used for cost reduction, and it is important to refine the structure of high-strength steel for the purpose of suppressing deterioration of ductility, toughness, durability ratio, etc. accompanying high tension. Has become a problem.

【0003】ところで、組織の微細化のために、従来か
ら用いられてきた方法をまとめると制御冷却法、大圧下
圧延法、制御圧延法などに区分される。これの製造技術
のうちでも、NbもしくはTiを含む鋼に制御圧延法を適用
した析出強化型高張力熱延鋼板は、高張力化と組織微細
化とを同時に達成するために有望な方法としてもっとも
広く用いられてきた。この方法が用いられた理由として
考えられることは、NbもしくはTiの析出強化作用によっ
て高張力化が容易に図れること、Nb、Tiのオーステナイ
ト粒の再結晶抑制作用を利用して、未再結晶オーステナ
イト粒に低温圧延を施した時のγ→α歪誘起変態を促進
させることによって、フェライト結晶粒を微細化する効
果を得ることができるためである。しかし、この方法で
製造された高張力熱延鋼板の難点は機械的性質の異方性
が大きいことである。このため例えば、プレス成形用の
自動車用鋼板などにおいては、成形限界はもっとも延性
が劣る方向での特性水準によって支配されるので、異方
性が大きい鋼板では高いプレス性を確保することが困難
になる。また、構造材あるいはパイプ材においても、重
要な特性である靭性や疲労強度などの異方性が大きいと
同様の問題につながる。
By the way, in order to miniaturize the structure, the methods conventionally used can be classified into a controlled cooling method, a large reduction rolling method, a controlled rolling method and the like. Among these manufacturing technologies, the precipitation-strengthened high-strength hot-rolled steel sheet obtained by applying the controlled rolling method to the steel containing Nb or Ti is the most promising method for simultaneously achieving high tensile strength and microstructure refinement. It has been widely used. The reason why this method was used is that precipitation strengthening action of Nb or Ti can easily achieve high tension, and the recrystallization suppressing action of austenite grains of Nb and Ti is utilized to obtain unrecrystallized austenite. This is because it is possible to obtain the effect of refining the ferrite crystal grains by promoting the γ → α strain-induced transformation when the grains are subjected to low-temperature rolling. However, a drawback of the high-strength hot-rolled steel sheet produced by this method is that the anisotropy of mechanical properties is large. For this reason, for example, in automotive steel sheets for press forming, the forming limit is governed by the characteristic level in the direction of the least ductility, so it is difficult to secure high pressability with steel sheets with large anisotropy. Become. Also in structural materials or pipe materials, if the anisotropy such as toughness and fatigue strength, which are important characteristics, is large, the same problem will occur.

【0004】一方、大圧下圧延による組織微細化法とし
て、例えば、特開昭58-1238232号公報などに代表される
提案がある。これらの方法における微細化機構の要点
は、オーステナイト粒に大圧下を加えることによってγ
→αへの歪誘起変態を促進することにあり、上記のNb、
Tiを含む析出強化鋼板の場含と基本的には同じ機構を利
用するものである。だだし、両者の違いは析出強化鋼で
はNb、Tiのオーステナイト粒の再結晶抑制効果を利用す
ることが要件となるのに対して、特開昭58-1238232号公
報の大圧下圧延法ではNb、Tiを含有させなくとも結晶粒
の微細化が可能であるということである。そのため、機
械的性質の異方性は析出強化鋼に比べて改善されるとい
う利点が生じる。しかし、この方法は、1パスあたりの
圧下量を40%以上にするなど、一般的なホットストリ
ップミルで実施し難いことが最大の難点である。また、
この方法によって微細なフェライト組織を得ることはで
きるとしても、高強度化を同時に達成することが難しい
ことも欠点である。
On the other hand, as a structure refining method by large reduction rolling, for example, there is a proposal represented by JP-A-58-1238232. The main point of the refinement mechanism in these methods is that by applying a large reduction to the austenite grains,
→ It is to promote the strain-induced transformation to α.
It basically uses the same mechanism as the case of precipitation strengthened steel sheet containing Ti. However, the difference between the two is that in precipitation strengthened steel, Nb, it is necessary to utilize the recrystallization suppression effect of austenite grains of Ti, whereas in the large reduction rolling method of JP-A-58-1238232, Nb That is, it is possible to make the crystal grains fine without containing Ti. Therefore, there is an advantage that the anisotropy of mechanical properties is improved as compared with precipitation strengthened steel. However, the most difficult point of this method is that it is difficult to carry out with a general hot strip mill, such as a reduction amount of 40% or more per pass. Also,
Although a fine ferrite structure can be obtained by this method, it is also a drawback that it is difficult to achieve high strength at the same time.

【0005】[0005]

【発明が解決しようとする課題】このように従来の製造
方法では、機械特性の異方性が大きいとか、高強度を得
にくいとか、また実操業が困難であるといった様々な問
題があった。
As described above, the conventional manufacturing method has various problems such as large anisotropy of mechanical properties, difficulty in obtaining high strength, and difficulty in actual operation.

【0006】この発明の目的は、上記既知技術が抱えて
いた問題点を解決する製造方法、具体的には、一般のホ
ットストリップミルで容易に実施することが可能で、か
つ機械的性質の異方性が少ない高張力熱延鋼板の製造方
法を提供することを目的とする。また、この発明の目的
は、高張力とくにTSが490 MPa 級以上の高強度範囲に
おいて、従来技術よりもフェライト結晶粒径の微細化を
一層高めることにより、延性、靭性、疲労強度を格段に
高めることができる高張力熱延鋼板の製造方法を提供す
ることを目的とする。
An object of the present invention is to provide a manufacturing method which solves the problems of the above-mentioned known techniques, and more specifically, it can be easily carried out by a general hot strip mill and has different mechanical properties. It is an object of the present invention to provide a method for producing a high-strength hot-rolled steel sheet having a low degree of orientation. Further, an object of the present invention is to significantly enhance ductility, toughness and fatigue strength by further miniaturizing the ferrite crystal grain size as compared with the prior art in a high tensile strength, particularly in a high strength range of TS of 490 MPa or more. An object of the present invention is to provide a method for producing a high-strength hot-rolled steel sheet that can be manufactured.

【0007】[0007]

【課題を解決するための手段】さて発明者らは、従来技
術においてフェライト結晶粒径の微細化手段として利用
されたγ→αの歪誘起変態を採用する限り、上記のよう
な問題点を回避することができないと考え、新たなる結
晶粒の微細化方法を探求し、本発明を完成するに至っ
た。すなわち、本発明の要旨構成は次のとおりである。
The present inventors avoid the above problems as long as the γ → α strain-induced transformation used as a means for refining the ferrite crystal grain size in the prior art is adopted. It was thought that it could not be achieved, and a new method of refining crystal grains was sought, and the present invention was completed. That is, the gist configuration of the present invention is as follows.

【0008】(1) C:0.05〜 0.30 wt%、 Si:2.0 wt
%以下、Mn:1.0 〜2.5 wt%、 Al:0.05wt%以下、
を含み、かつTi:0.05〜0.3 wt%、 Nb:0.10wt%以
下、のうちの1種または2種を含有し、残部がFeおよび
不可避的不純物よりなる鋼を、950〜1100℃の温
度に加熱した後、1回当りの圧下量が20%以上となる
圧下を少なくとも2回以上加え、仕上げ温度がAr3変態
点以上になるように熱間圧延し、Ar3変態点〜750℃
の温度範囲を20℃/sec 以上の速度で冷却し、続いて
750℃未満〜600℃の温度範囲において、10℃/
sec 以下の速度で冷却して、5〜20sec の時間滞留さ
せた後、再び20℃/sec 以上の速度で550℃以下の
温度まで冷却し、550℃以下の温度でコイルに巻取る
ことを特徴とするフェライト体積率が80%以上で、平
均フェライト粒径が10μm未満の極微細組織を有する
高張力熱延鋼板の製造方法。
(1) C: 0.05 to 0.30 wt%, Si: 2.0 wt
% Or less, Mn: 1.0 to 2.5 wt%, Al: 0.05 wt% or less,
Steel containing at least one of Ti: 0.05 to 0.3 wt% and Nb: 0.10 wt% or less, with the balance consisting of Fe and inevitable impurities at a temperature of 950 to 1100 ° C. After heating, a reduction amount of 20% or more per time is applied at least twice, and hot rolling is performed so that the finishing temperature is the Ar 3 transformation point or more, and the Ar 3 transformation point to 750 ° C.
In the temperature range of less than 750 ° C to 600 ° C, 10 ° C /
After cooling at a rate of less than sec and staying for 5 to 20 seconds, it is cooled again to a temperature of 550 ° C or less at a rate of 20 ° C / sec or more and wound on a coil at a temperature of 550 ° C or less. A method for producing a high-strength hot-rolled steel sheet having an ultrafine structure having a ferrite volume ratio of 80% or more and an average ferrite grain size of less than 10 μm.

【0009】(2) C:0.05〜 0.30 wt%、 Si:2.0 wt
%以下、Mn:1.0 〜2.5 wt%、 Al:0.05wt%以下、
を含み、かつTi:0.05〜0.3 wt%、 Nb:0.10wt%以
下、のうちの1種または2種を含有し、さらにCr:1.5
wt%以下、 Cu:1.5 wt%以下、Ni:1.5 wt%以下、
Mo:1.5 wt%以下から選ばれる1種または2種以上
を含有し、残部がFeおよび不可避的不純物よりなる鋼
を、950〜1100℃の温度に加熱した後、1回当り
の圧下量が20%以上となる圧下を少なくとも2回以上
加え、仕上げ温度がAr3変態点以上になるように熱間圧
延し、Ar3変態点〜750℃の温度範囲を20℃/sec
以上の速度で冷却し、続いて750℃未満〜600℃の
温度範囲において、10℃/sec 以下の速度で冷却し
て、5〜20sec の時間滞留させた後、再び20℃/se
c 以上の速度で550℃以下の温度まで冷却し、550
℃以下の温度でコイルに巻取ることを特徴とするフェラ
イト体積率が80%以上で、平均フェライト粒径が10
μm未満の極微細組織を有する高張力熱延鋼板の製造方
法。
(2) C: 0.05 to 0.30 wt%, Si: 2.0 wt
% Or less, Mn: 1.0 to 2.5 wt%, Al: 0.05 wt% or less,
And one or two of Ti: 0.05 to 0.3 wt%, Nb: 0.10 wt% or less, and Cr: 1.5 wt% or less.
wt% or less, Cu: 1.5 wt% or less, Ni: 1.5 wt% or less,
Mo: A steel containing one or more selected from 1.5 wt% or less, the balance of which is Fe and unavoidable impurities, is heated to a temperature of 950 to 1100 ° C., and the reduction amount per time is 20. % or more and consisting reduction added at least twice, were hot rolled to finishing temperature becomes higher Ar 3 transformation point, the temperature range of Ar 3 transformation point to 750 ° C. 20 ° C. / sec
After cooling at the above rate, and subsequently in the temperature range of less than 750 ° C to 600 ° C, cooling at a rate of 10 ° C / sec or less, and allowing it to stay for 5 to 20 seconds, 20 ° C / se again.
Cool to a temperature of 550 ° C or less at a rate of c
The ferrite volume ratio is 80% or more, and the average ferrite grain size is 10%, which is characterized by being wound around a coil at a temperature of ℃ or less.
A method for producing a high-strength hot-rolled steel sheet having an ultrafine structure of less than μm.

【0010】[0010]

【発明の実施の形態】本発明における結晶粒の微細化方
法は、以下に述べる2つの手段を組み合わせることを基
本としている。その第1の手段は再結晶を利用すること
であり、第2手段は圧延後の制御冷却を利用することで
ある。
BEST MODE FOR CARRYING OUT THE INVENTION The grain refining method of the present invention is based on the combination of the following two means. The first means is to utilize recrystallization and the second means is to use controlled cooling after rolling.

【0011】まず、第1の手段について詳述する。オー
ステナイト粒が熱間圧延において微細化してゆく過程と
して、圧延一再結晶による微細化過程があることは古く
から知られている。しかし、一般にはこのような再結晶
による微細化では、到達し得るフェライト結晶粒径はせ
いぜい20μmが限度である。これに対して、上記の制
御圧延法や大圧下圧延法によると10μm程度の微細粒
を得ることができるので、再結晶過程を利用する微細化
方法は極微細組織を得る手段としては不適当であると考
えられてきた。しかし、発明者らは、熱延開始前のオー
ステナイト粒径、すなわちスラブ加熱時点でのオーステ
ナイト粒径を極度に微細化させてから圧延を行うと、そ
の後の圧延一再結晶が極めて加速的に生じるようにな
り、しかも圧延後の再結晶粒の微細化が大幅に進展する
ことを発見したのである。この理由については必ずしも
明確ではないが、次に述べる機構によると考えられる。
First, the first means will be described in detail. It has long been known that there is a refinement process by rolling-recrystallization as a process in which austenite grains are refined in hot rolling. However, in general, the grain size of ferrite crystal that can be reached by such refining by recrystallization is at most 20 μm. On the other hand, according to the above-described controlled rolling method or large reduction rolling method, fine grains of about 10 μm can be obtained, so the refining method utilizing the recrystallization process is unsuitable as a means for obtaining an ultrafine structure. It has been thought that there is. However, the inventors have found that if the austenite grain size before the start of hot rolling, that is, the austenite grain size at the time of slab heating is extremely refined before rolling, the subsequent rolling-recrystallization is extremely accelerated. It was discovered that the refinement of recrystallized grains after rolling significantly progressed. The reason for this is not clear, but it is thought to be due to the mechanism described below.

【0012】圧延によるオーステナイト粒の再結晶には
動的再結晶と静的再結晶とがあり、このうち前者は圧下
温度が高く、歪速度が遅く、かつ大圧下が加えられる
時、すなわち、ホットストリップミルでの熱延でいえば
一般的には粗圧延の初期〜中期の段階に該当するような
圧延条件においてのみ生じる可能性のある再結晶であ
り、圧延温度が低下し、かつ歪速度の速くなる仕上げ圧
延の段階になるとこの動的再結晶は起き難くなり、代わ
りに静的再結晶が起きるようになると考えられてきた。
ところで、動的再結晶は極めて速い速度での粒界移動あ
るいは粒界の新たな生成によって歪を開放する現象であ
る。結晶粒の微細化は粒界移動を容易化するので動的再
結晶を生じ易くする方向に作用する。また、動的再結晶
粒の核生成は旧粒界であるので、旧粒が微細であるほど
動的再結晶粒の核生成頻度が高まり、再結晶後の新粒の
微細化が進行するはずである。かくして、初期オーステ
ナイト粒径を極度に微細化すれば、動的再結晶はより低
温域、より高歪速度域、より低歪量域においても生じる
ようになり、従来の熱延では生じ得なかった仕上げ圧延
段階においても動的再結晶が起こるようになり、圧下数
の増加とともに動的再結晶による微細化が進行してゆく
ものと推測される。
Recrystallization of austenite grains by rolling includes dynamic recrystallization and static recrystallization. Of these, the former has a high reduction temperature, a low strain rate, and a large reduction, that is, a hot reduction. Generally speaking, hot rolling in a strip mill is a recrystallization that may occur only under rolling conditions corresponding to the initial to middle stages of rough rolling, and the rolling temperature decreases and strain rate It has been considered that this dynamic recrystallization becomes difficult to occur at the stage of finish rolling which becomes faster, and static recrystallization instead occurs.
By the way, dynamic recrystallization is a phenomenon in which strain is released by movement of grain boundaries or generation of new grain boundaries at an extremely high speed. The refinement of crystal grains facilitates the movement of grain boundaries, and thus acts in the direction of facilitating dynamic recrystallization. Also, since the nucleation of dynamic recrystallized grains is at the old grain boundary, the finer the older grains, the higher the frequency of nucleation of dynamic recrystallized grains, and the more refined the new grains after recrystallization should be Is. Thus, if the initial austenite grain size is extremely refined, dynamic recrystallization will occur even in the lower temperature region, the higher strain rate region, and the lower strain amount region, which could not occur in the conventional hot rolling. It is presumed that dynamic recrystallization will occur even in the finish rolling stage, and miniaturization due to dynamic recrystallization will progress as the number of reductions increases.

【0013】上記の微細化機構において、もっとも重要
な点は、いうまでもなくスラブ加熱段階における初期オ
ーステナイト粒を極度に微細化させることである。本発
明ではこのための手段として、多量のTiCを存在せしめ
ることによって達成する。なお、上記した従来の析出強
化鋼においてもTiを微細化元素として利用するが、本発
明でのTiの作用と析出強化鋼におけるそれとは明白に異
なる。すなわち、従来のTi系析出強化鋼におけるTiの作
用には、スラブ加熱段階ではオーステナイトに溶体化さ
せ、固溶Tiとしての再結晶抑制効果を利用して微細化作
用を発現させることと、変態した後のフェライト粒に微
細なTiCとして再析出させて析出強化を引きださせるこ
ととが含まれる。Nb系析出強化鋼においてはNbがこの役
割を果たす。したがって、析出強化鋼においてはスラブ
加熱段階でTiC、もしくはNbCを溶解させることが必要
であり、加熱温度として比較的高温であることが必須と
なる。これに対して、本発明ではTiをスラブ加熱段階で
オーステナイトに溶解させずTiCの状態として存在させ
ることが重要である。この理由は、第1に固溶Tiは再結
晶を阻害し、本発明の微細化過程である動的再結晶を起
こし難くするためであり、第2に初期オーステナイトの
成長を抑制するTiCの量がその溶解によって減ずるから
である。そのため、本発明ではスラブ加熱温度をTiCの
溶解が生じない低温域に設定することが必須の要件とな
るのである。
Needless to say, the most important point in the above-mentioned miniaturization mechanism is to extremely miniaturize the initial austenite grains in the slab heating stage. In the present invention, a means for this purpose is achieved by allowing a large amount of TiC to be present. Although Ti is used as a refining element also in the above-mentioned conventional precipitation-strengthened steel, the action of Ti in the present invention and that in precipitation-strengthened steel are clearly different. That is, the action of Ti in the conventional Ti-based precipitation-strengthened steel, the slab heating stage solutionized to austenite, to express the refining action by utilizing the recrystallization suppression effect as solid solution Ti, and transformed Re-precipitation as fine TiC in the subsequent ferrite grains to induce precipitation strengthening is included. Nb plays this role in Nb-based precipitation strengthened steel. Therefore, in precipitation strengthened steel, it is necessary to melt TiC or NbC in the slab heating stage, and it is essential that the heating temperature is relatively high. On the other hand, in the present invention, it is important that Ti is not dissolved in austenite in the slab heating stage and is present as TiC. This is because, firstly, solid solution Ti inhibits recrystallization and makes it difficult to cause dynamic recrystallization, which is the refinement process of the present invention. Secondly, the amount of TiC that suppresses the growth of initial austenite. Is reduced by its dissolution. Therefore, in the present invention, it is an essential requirement to set the slab heating temperature to a low temperature range where TiC melting does not occur.

【0014】次に、本発明における第2の微細化手段で
ある制御冷却について述べる。従来技術における制御冷
却による組織微細化手段は、多くの場合、制御圧延もし
くは大圧下圧延法などと組み台わせて、それを補完する
手段として用いられてきた。例えば、特公昭64-7131 号
公報もその代表例である。この提案における制御冷却方
法は、所定の圧延を行った後「20〜1000℃/sec
の冷却速度で500℃以下まで冷却する」ことであり、
その技術思想は圧延後はフェライト結晶粒の成長が生じ
ない温度範囲まで急冷するという単純な考え方に基づい
ている。これに対し、本発明での制御冷却の特徴は、冷
却途上において生じるγ→α変態領域、すなわち、CC
T変態曲線におけるフェライトノーズ近傍の温度領域に
おいて、急冷をいったん停止して緩冷却期間を設け、そ
の後再び急冷を施す点にある。本発明者らはこの冷却途
上の所定温度範囲で緩冷却期を設けることにより、組織
の微細化が一層高まることを見い出したのであるが、こ
のような現象が現れる理由について次のように推察し
た。
Next, the controlled cooling which is the second miniaturization means in the present invention will be described. In many cases, the structure refining means by controlled cooling in the prior art has been used as a means for complementing it by combining it with a controlled rolling method or a large reduction rolling method. For example, Japanese Examined Patent Publication No. Sho 64-7131 is a typical example. The controlled cooling method in this proposal is "20 to 1000 ° C / sec after performing predetermined rolling.
At a cooling rate of less than 500 ° C. ”
The technical idea is based on the simple idea of quenching to a temperature range where the growth of ferrite crystal grains does not occur after rolling. On the other hand, the feature of the controlled cooling in the present invention is that the γ → α transformation region that occurs during cooling, that is, CC
In the temperature region near the ferrite nose in the T transformation curve, the rapid cooling is once stopped to provide a slow cooling period, and then the rapid cooling is performed again. The present inventors have found that by providing a slow cooling period within this predetermined temperature range during cooling, the refinement of the structure is further enhanced. The reason why such a phenomenon appears is speculated as follows. .

【0015】γ→α変態の進行は核生成と成長により進
行することはよく知られた点であるが、本発明のように
最終組織をフェライト主体の組織とする場合、そのフェ
ライト粒の微細化度を決定する因子としては、生成した
フェライト核の数の多さが支配的であると考えられる。
この核生成がもっとも活発に生じる変態領域は、フェラ
イト変態速度がもっとも大きくなる領域であり、CCT
曲線におけるフェライトノーズ近傍がそれに該当する領
域であることが経験的にも理解できる。このことから明
かなように、フェライトノーズ近傍で緩冷却期間を設け
ることの意義はフェライト変態核の生成がもっとも活発
になる温度領域で変態を進行させるという点にあり、こ
のことによって最終組織のフェライト粒の微細化が進展
するものと考えられる。また、付帯的効果として、以上
のような制御冷却を採用することによって、2相(D
P)組織や残留γ組織が得られ易くなり、組織微細化と
高強度化とを同時に達成する手段として利用することが
できる利点が生じる。
It is well known that the γ → α transformation proceeds by nucleation and growth, but when the final structure is mainly composed of ferrite as in the present invention, the ferrite grains are refined. It is considered that the number of ferrite nuclei formed is dominant as a factor that determines the degree.
The transformation region in which this nucleation occurs most actively is the region in which the ferrite transformation speed becomes the highest, and the CCT
It can be empirically understood that the vicinity of the ferrite nose in the curve is the corresponding region. As is clear from this, the significance of providing a slow cooling period in the vicinity of the ferrite nose is that the transformation proceeds in the temperature region in which the ferrite transformation nuclei are most actively generated, which allows the ferrite of the final structure to be formed. It is considered that grain refinement progresses. In addition, as an incidental effect, the two-phase (D
P) The structure and the residual γ structure are easily obtained, and there is an advantage that it can be used as a means for simultaneously achieving the refinement of the structure and the enhancement of the strength.

【0016】本発明は、以上詳述したように、圧延によ
るオーステナイト粒の動的再結晶による微細化技術と、
γ→α変態に際しフェライト核生成域での緩冷却を採り
入れた制御冷却技術の2つの技術を組み台わせることに
よって、従来技術では達成できなかった範囲の極微細フ
ェライト粒を形成させ得ることを見い出し、完成するに
至ったものである。次に、本発明における鋼の成分組成
および製造条件を前記構成要件に示す範囲に定めた理由
について説明する。
As described in detail above, the present invention provides a refinement technique by dynamic recrystallization of austenite grains by rolling,
It is possible to form ultrafine ferrite grains in a range that could not be achieved by conventional techniques by combining two techniques of controlled cooling technique that incorporates slow cooling in the ferrite nucleation region during the γ → α transformation. It was discovered and completed. Next, the reasons why the steel composition and manufacturing conditions in the present invention are set within the ranges shown in the above structural requirements will be described.

【0017】C:0.05〜 0.30 wt% Cは、強度を確保するために、また組織の微細化達成に
加熱段階で必要な十分な量のTiCを確保するために0.05
wt%以上が必要である。しかし、 0.30 wt%を超えて添
加すると第2相の比率が多くなり、延性および靭性が劣
化するとともに、溶接性も悪化する。したがって、Cは
0.05〜 0.30 wt%、好ましくは0.07〜0.20wt%の範囲と
する。
C: 0.05 to 0.30 wt% C is 0.05 in order to secure the strength and to secure a sufficient amount of TiC necessary in the heating stage to achieve the refinement of the structure.
wt% or more is required. However, if added in excess of 0.30 wt%, the proportion of the second phase increases, and the ductility and toughness deteriorate and the weldability also deteriorates. Therefore, C is
The range is 0.05 to 0.30 wt%, preferably 0.07 to 0.20 wt%.

【0018】Si:2.0 wt%以下 Siは、固溶強化により、強度一伸びバランスを改善しつ
つ強度を高める有効な元素であるほか、フェライト変態
を促進して、目標とする80%以上のフェライト体積率
をもつ組織を得る上で有効な作用を発揮する元素である
が、熱延時に脱スケール性の悪いスケールを生じ、製品
の表面性状に悪影響を及ぼしやすい元素でもある。この
悪影響はSi量が多いほど、また加熱温度が高いほど顕著
になることが知られている。本発明においては極微細組
織化のために加熱温度を低温域に設定するので、通常の
鋼に比べて表面性状が悪化するSi量の上限は通常の鋼に
比べて高くできるものの、2.0 wt%を超えるとその悪影
響が顕在化する。したがって、Siは2.0 wt%以下とす
る。なお、好ましい含有範囲は0.3 〜1.6wt%の範囲で
ある。
Si: 2.0 wt% or less Si is an effective element for improving strength-stretch balance while improving strength-strength balance by solid solution strengthening, and promotes ferrite transformation to achieve a target of 80% or more ferrite. Although it is an element that exerts an effective action in obtaining a structure having a volume fraction, it is also an element that easily produces a scale with poor descaling property during hot rolling and tends to adversely affect the surface properties of the product. It is known that this adverse effect becomes more significant as the amount of Si increases and the heating temperature increases. In the present invention, since the heating temperature is set to a low temperature range for ultrafine structure, the upper limit of the amount of Si in which the surface properties are deteriorated as compared with ordinary steel can be made higher than that of ordinary steel, but 2.0 wt% When it exceeds, the adverse effect becomes apparent. Therefore, Si should be 2.0 wt% or less. The preferable content range is 0.3 to 1.6 wt%.

【0019】Mn:1.0 〜2.5 wt% Mnは、第2相の変態組織に影響を与えて強度を高める上
で必須の元素であり、1.0 wt%以上必要であるが、2.5
wt%を超えて添加するとフェライト変態が遅延し、本発
明の狙いとする80%以上のフェライト体積率をもつ組
織が得難くなる。したがって、Mnの添加量は1.0 〜2.5
wt%、好ましくは1.2 〜2.0 wt%の範囲とする。
Mn: 1.0-2.5 wt% Mn is an essential element for affecting the transformation structure of the second phase and increasing the strength, and is required to be 1.0 wt% or more.
If it is added in excess of wt%, ferrite transformation will be delayed and it will be difficult to obtain a structure having a ferrite volume ratio of 80% or more, which is the aim of the present invention. Therefore, the amount of Mn added is 1.0 to 2.5.
wt%, preferably 1.2 to 2.0 wt%.

【0020】Al:0.05wt%以下 Alは、脱酸元素として通常0.010 〜0.10wt%の範囲で含
有させるのが一般的であるが、一方においてこのような
Alキルド鋼では溶鋼の鋳型への鋳込み中の再酸化によっ
て生じたAl2O3 がノズル詰まりや鋳片への混入による清
浄度の悪化を招く。このため鋳込み速度の上昇などの生
産性を高める手段が取れないなどの弊害を生じている。
このような弊害は、Alが0.05wt%を超えると特に著しく
なる。これに対し、本発明ではSiおよびTiを添加するこ
とを前提としているので、これらの元素の添加により溶
鋼の平衡酸素量が十分に低下するため、脱酸元素として
のAlの必要性は従来鋼よりも少なく、むしろ、必要以上
のAl添加は固溶Alを増加させ、オーステナイト粒の動的
再結晶を阻害するなどの悪影響が現れる。このような問
題を回避するためには、Al量は0.05wt%以下、好ましく
は0.01wt%以下とする必要がある。
Al: 0.05 wt% or less Al is generally contained in the range of 0.010 to 0.10 wt% as a deoxidizing element.
In Al-killed steel, Al 2 O 3 generated by reoxidation of molten steel during casting into the mold causes nozzle clogging and deterioration of cleanliness due to mixing into the slab. For this reason, there is an adverse effect such that the means for improving productivity such as an increase in casting speed cannot be taken.
Such an adverse effect becomes particularly remarkable when Al exceeds 0.05 wt%. On the other hand, in the present invention, since it is premised that Si and Ti are added, the equilibrium oxygen content of the molten steel is sufficiently reduced by the addition of these elements. Less than that, rather, excessive addition of Al increases solid solution Al, and adverse effects such as inhibiting dynamic recrystallization of austenite grains appear. In order to avoid such a problem, the amount of Al needs to be 0.05 wt% or less, preferably 0.01 wt% or less.

【0021】Ti:0.05〜0.3 wt%、Nb:0.10wt%以下 Tiは、前述したように、TiCとして存在させてスラブ加
熱段階での初期オーステナイト粒を微細化させ、以降の
圧延過程での動的再結晶を生じさせる上で必須の元素で
ある。この作用を発揮させるためには少なくとも0.05wt
%以上必要であり、TiC量の増加ととも微細化効果は大
きくなる。しかし、0.3 wt%を超えて添加しても飽和す
るので、0.05〜0.3 wt%、好ましくは0.07〜0.20wt%の
範囲とする。なお、本発明では従来の析出強化鋼などに
比べるとTiの添加量を比較的多くすることに特徴がある
が、このことはフェライト体積率を高める上で次のよう
な好ましい作用を及ぼす。すなわち、TiCとして鋼中の
Cの一部が固定されるために、変態第2相を形成するC
量はその分だけ少なくなり、最終のミクロ組織中に占め
るフェライト体積率が相対的に高くなるのである。この
ことは後述するように延性、低温靭性および疲労特性を
高める上で有効に寄与する。
Ti: 0.05 to 0.3 wt%, Nb: 0.10 wt% or less As described above, Ti is present as TiC to refine the initial austenite grains in the slab heating stage and to reduce the dynamics in the subsequent rolling process. It is an essential element to cause recrystallization. At least 0.05wt to exert this effect
% Or more, and the refinement effect becomes large with an increase in the TiC amount. However, even if added in excess of 0.3 wt%, it saturates, so the range is set to 0.05 to 0.3 wt%, preferably 0.07 to 0.20 wt%. The present invention is characterized in that the addition amount of Ti is relatively large as compared with the conventional precipitation strengthened steel and the like, but this has the following preferable effect in increasing the ferrite volume ratio. That is, since a part of C in the steel is fixed as TiC, C that forms the transformation second phase
The amount is reduced accordingly and the volume fraction of ferrite in the final microstructure is relatively high. This effectively contributes to the enhancement of ductility, low temperature toughness and fatigue properties as described later.

【0022】また、本発明におけるTiと同様の作用を示
す元素としてNbがある。このNbをTiと代替するか、もし
くはTiに重畳して使用することによっても良好な効果が
得られる。ただし、このNbの効果は、Cに対する原子比
当量当りでみると、Tiの作用とほぼ等価であるので、重
量比ではTiのおおよそ2倍の添加が必要となる。そのう
え、現時点ではTiよりも高価な元素であるので経済的に
はメリットが少ない。しかし、ERW溶接あるいはフラ
ッシュバット溶接などの溶接が施される用途では、溶接
接合界面での酸化物の残存が問題となる場合ある。この
ときには、TiにかえてNbを使用する方が有利となること
もある。このような用途、目的に対してはNbの添加もあ
り得る。この場合に、Nbの効果は0.10を超えると飽和す
るので0.10wt%以下とする。
Further, Nb is an element having the same action as Ti in the present invention. A good effect can also be obtained by substituting Nb for Ti or by superposing it on Ti. However, the effect of Nb is almost equivalent to the effect of Ti when viewed in terms of atomic ratio equivalent to C, so that it is necessary to add approximately twice the weight ratio of Ti. Moreover, since it is an element that is more expensive than Ti at the present time, it has little economic advantage. However, in applications where welding such as ERW welding or flash butt welding is performed, the residual oxide at the welded joint interface may be a problem. In this case, it may be advantageous to use Nb instead of Ti. Nb may be added for such purposes and purposes. In this case, the effect of Nb is saturated when it exceeds 0.10, so 0.10 wt% or less is set.

【0023】上記の基本成分の他に、さらに、Cr、Cu、
Ni、Moのうちの少なくとも1種を含有させることもでき
る。これらの元素は、ほぼMnと同様な作用をもたらし、
所望の強度を確保するために必要に応じて添加する。ま
た、強度のほかに、例えば溶接性や耐食性を高める作用
を有するのでこれらの特性を向上させる場合に添加する
と効果的である。しかし、これらの元素はMnに比べて高
価であり、過度に添加するといずれも経済的に不利にな
るので、上記元素はそれぞれCr:1.5 wt%以下、Cu:1.
5 wt%以下、Ni:1.5 wt%以下、Mo:1.5 wt%以下の範
囲で添加するものとする。
In addition to the above basic components, Cr, Cu,
It is also possible to contain at least one of Ni and Mo. These elements bring about the same action as Mn,
Add as necessary to ensure the desired strength. Further, in addition to the strength, it has an action of enhancing, for example, weldability and corrosion resistance, so that it is effective to add it when improving these properties. However, these elements are more expensive than Mn, and if added excessively, both are economically disadvantageous, so the above elements are Cr: 1.5 wt% or less, Cu: 1.
5 wt% or less, Ni: 1.5 wt% or less, Mo: 1.5 wt% or less.

【0024】・加熱条件 本発明においては、TiCによる初期オーステナイト粒の
微細化効果を最大限に発揮させることが技術上の重要な
ポイントであり、そのための条件として950〜110
0℃の範囲で加熱する必要がある。すなわち、加熱温度
が1100℃を超えると、TiCのオーステナイトヘの溶
解量が増加し、オーステナイト粒径を微細化する効果が
失われるとともに、固溶Tiの増加によって圧延時の動的
再結晶が生じ難くなり、目的とする高いフェライト分率
と極微細なフェライト粒径が得られず、従来技術による
熱延鋼板なみの機械的性質しか得られなくなるためであ
る。一方、その温度が950℃未満になると、仕上圧延
をオーステナイト領域で終えることが難しくなり、目標
とするミクロ組織と機械的性質を確保し難くなるためで
ある。なお、本発明者らはもっとも好ましい加熱温度範
囲はTiとCの溶解度積から求まると考え、実験的に調査
した結果、下記(1)式で示される温度(SRT)を基
準として+20℃〜−100℃の範囲であることがわか
った。 SRT(℃)=−10475 /[ log{total Ti(%) − 1.5S(%) − 3.4N(%) } −5.33 ]+273 ・・・・・(1)
Heating Conditions In the present invention, it is a technically important point to maximize the effect of refining the initial austenite grains by TiC, and the conditions therefor are 950 to 110.
It is necessary to heat in the range of 0 ° C. That is, when the heating temperature exceeds 1100 ° C., the amount of TiC dissolved in austenite increases, the effect of refining the austenite grain size is lost, and the increase in solid solution Ti causes dynamic recrystallization during rolling. This is because it becomes difficult, and the desired high ferrite fraction and ultrafine ferrite grain size cannot be obtained, and only the mechanical properties similar to those of conventional hot-rolled steel sheets can be obtained. On the other hand, if the temperature is less than 950 ° C., it is difficult to finish the finish rolling in the austenite region, and it becomes difficult to secure the target microstructure and mechanical properties. The inventors of the present invention believe that the most preferable heating temperature range is obtained from the solubility product of Ti and C, and as a result of an experimental investigation, as a reference, the temperature (SRT) represented by the following formula (1) is + 20 ° C to- It was found to be in the range of 100 ° C. SRT (℃) =-10475 / [log {total Ti (%)-1.5S (%)-3.4N (%)}-5.33] +273 (1)

【0025】・熱間圧延条件 本発明では、熱間圧延によってオーステナイト粒に動的
再結晶を繰り返し生じさせて微細化を達成する。この動
的再結晶を惹起する初期条件は上記スラブ加熱温度要件
を満たすことによって保証されているので、圧延に際し
ての要件はまず、1回当りの圧下量が重要な要素とな
る。すなわち、この圧下量が20%に満たない場合には
目的とする動的再結晶による微細化が行われなくなるの
で、各圧延スタンド毎の圧下量の下限を20%にする。
上限は微細化効果の観点からは特に限定する必要はない
が、現実的には圧延機の圧下能力によって限界が生じ、
圧延温度、鋼の化学成分および圧延寸法などによって異
なるものの、20〜40%の圧下を施すことが可能な圧
延機が一般的であるので、本発明の要件を実施させるこ
とは容易である。
Hot Rolling Conditions In the present invention, the hot rolling causes the austenite grains to repeatedly undergo dynamic recrystallization to achieve the refinement. Since the initial conditions for inducing this dynamic recrystallization are ensured by satisfying the slab heating temperature requirement, the rolling reduction requirement is firstly an important factor. That is, if the reduction amount is less than 20%, the desired refinement by dynamic recrystallization will not be performed, so the lower limit of the reduction amount for each rolling stand is set to 20%.
The upper limit need not be particularly limited from the viewpoint of the refinement effect, but in reality, there is a limit due to the rolling capacity of the rolling mill,
Although it depends on the rolling temperature, the chemical composition of the steel, the rolling size, and the like, a rolling mill that can perform a reduction of 20 to 40% is common, and therefore it is easy to implement the requirements of the present invention.

【0026】また、動的再結晶を起こさせる回数が多く
なるほど微細化が進展するので、仕上げ圧延までの圧下
回数が重要であり、圧下回数が2回に満たない場合には
本発明の目的とする10μm未満の極微細粒フェライト
粒が得られなくなる。そのため、圧下回数の下限を2回
とする。なお、通常のホットストリップミルにおける圧
延での合計の圧下回数は通常10〜12パスであること
が多く、圧下回数として不足することはない。もちろ
ん、本発明を実施するには必ずしも10〜12パスの圧
延を行う必要はなく、たとえば、仕上げ圧延機もしくは
粗圧延機でのいくつかの圧下を省略して実施させること
も可能である。また、仕上げ温度はAr3変態点以上とす
る必要がある。これは、Ar3変態点未満の低温で熱間圧
延を終了すると熱間圧延時に生成していたフェライト粒
内に過度の転位が導入され、延性および靱性が悪化する
からである。
Further, as the number of times of causing dynamic recrystallization increases, the refinement progresses. Therefore, the number of reductions until the finish rolling is important, and when the number of reductions is less than two, the purpose of the present invention is to It becomes impossible to obtain ultrafine ferrite particles of less than 10 μm. Therefore, the lower limit of the number of times of rolling is set to 2 times. Note that the total number of reductions during rolling in a normal hot strip mill is usually 10 to 12 passes in many cases, and the number of reductions is not insufficient. Of course, in order to carry out the present invention, it is not always necessary to carry out rolling in 10 to 12 passes, and for example, it is possible to carry out by carrying out omitting some reductions in the finish rolling mill or the rough rolling mill. Further, the finishing temperature must be higher than the Ar 3 transformation point. This is because when hot rolling is completed at a low temperature below the Ar 3 transformation point, excessive dislocations are introduced into the ferrite grains formed during hot rolling, and ductility and toughness deteriorate.

【0027】・冷却条件 本発明法に従う条件で仕上げ圧延を終えたオーステナイ
ト粒は、ほぼ等軸の微細粒となっており、そのままγ→
α変態させても十分に微細なフェライト粒を得ることが
できるが、さらに極微細なフェライト粒とするためにラ
ンアウトテーブル上で制御冷却を施す。その制御冷却
は、初めにも述べたように、3段階の冷却区間からな
る。すなわち、第1段階は仕上げ圧延後Ar3変態点〜フ
ェライト変態核の発生頻度が高い温度域、すなわち75
0℃以下までを急冷する期間、第2段階はフェライト変
態核が活発に発生する温度領域(750℃未満〜600
℃) において所定時間滞留させ、フェライト変態核数を
高めるために緩冷する期間、第3段階は第2段階まで残
留γ相として存在していた第2相をパーライト、ベイナ
イトもしくはマルテンサイトなどの硬質第2相に変態さ
せるためもしくは残留γ相として残存させるための急冷
区間である。
Cooling conditions The austenite grains that have been finish-rolled under the conditions according to the method of the present invention are substantially equiaxed fine grains, and γ →
Even if α-transformed, sufficiently fine ferrite grains can be obtained, but controlled cooling is performed on the run-out table in order to make the ferrite grains extremely fine. The control cooling consists of three stages of cooling sections, as described above. That is, the first stage is a temperature range in which the Ar 3 transformation point after finish rolling to the frequency of occurrence of ferrite transformation nuclei is high, that is, 75
During the period of rapid cooling down to 0 ° C or less, the second stage is a temperature range in which ferrite transformation nuclei are actively generated (less than 750 ° C to 600
C.) for a predetermined time and then slowly cooled to increase the number of ferrite transformation nuclei. In the third step, the second phase that was present as the residual γ phase until the second step was hardened by pearlite, bainite or martensite. This is a quenching section for transforming into the second phase or remaining as the residual γ phase.

【0028】まず、第1段階の冷却では、仕上げ圧延後
Ar3変態点〜750℃までの区問の冷却速度を20℃/
sec の条件で行う。この理由は、750℃以上で生じる
γ→α変態の核生成速度は小さく、γ→α変態の進行が
数少ないフェライト粒の粒成長によって主に進行するの
で、フェライト粒径が大きくなり易く、粒成長によるγ
→α変態を阻止するためには、この区問における冷却速
度を20℃/sec 以上とする必要があるからである。な
お、この区問における冷却速度は40〜100℃/sec
の範囲とするのが望ましい。
First, in the first-stage cooling, the cooling rate in the zone from the Ar 3 transformation point to 750 ° C. after finish rolling is 20 ° C. /
Perform under the condition of sec. The reason for this is that the nucleation rate of the γ → α transformation that occurs at 750 ° C. or higher is small, and the progress of the γ → α transformation is mainly due to the grain growth of ferrite grains, so that the ferrite grain size tends to be large and the grain growth Due to γ
→ In order to prevent the α transformation, it is necessary to set the cooling rate in this section to 20 ° C / sec or more. The cooling rate in this section is 40 to 100 ° C / sec.
It is desirable to be within the range.

【0029】第2段階の冷却では、750℃未満〜60
0℃の温度域を10℃/sec 以下の速度で冷却してこの
温度域で5〜20秒問滞留させる。この理由は、γ→α
変態は核生成速度が大きい750未満〜600℃の温度
域で、極微細フェライト粒を得る上でもっと重要なフェ
ライト変態核の数を多くすることができるためである。
すなわち、750℃以上または600℃未満では、いず
れもフェライト核の生成速度が小さくなって好ましくな
いので750未満〜600℃の温度域とする。なお、こ
の温度域のうちより望ましいのは700〜650℃の範
囲である。また、上記温度域での冷却速度を10℃/se
c 以下とするのは、核生成に対して良好な温度範囲を逸
脱せずに5〜20秒間滞留させるために必要な条件とな
るからである。滞留時間を5〜20秒間とする理由は5
秒未満ではフェライト変態核数を増加させつつ最終組織
のフェライト体積率を目標の80%以上まで高めるには
不十分であるからであり、20秒を超えて滞留させてた
場合には狙いとする効果が飽和してしまうからである。
この範囲で望ましいの7秒以上である。
In the second stage cooling, less than 750 ° C. to 60 ° C.
The temperature range of 0 ° C. is cooled at a rate of 10 ° C./sec or less and allowed to stay in this temperature range for 5 to 20 seconds. The reason for this is γ → α
This is because the transformation can increase the number of ferrite transformation nuclei, which is more important for obtaining ultrafine ferrite grains, in the temperature range of less than 750 to 600 ° C. where the nucleation rate is high.
That is, if the temperature is 750 ° C. or higher or lower than 600 ° C., the rate of generation of ferrite nuclei is low, which is not preferable. It is to be noted that the more preferable temperature range is 700 to 650 ° C. The cooling rate in the above temperature range is 10 ° C / se
The reason for setting c or less is that it is a condition necessary for staying for 5 to 20 seconds without deviating from a favorable temperature range for nucleation. The reason why the residence time is 5 to 20 seconds is 5
This is because if it is less than 2 seconds, it is not sufficient to increase the ferrite transformation nucleus number and increase the ferrite volume fraction of the final structure to 80% or more of the target, and if it is retained for more than 20 seconds, it is aimed. This is because the effect will be saturated.
It is preferably 7 seconds or more in this range.

【0030】なお、この第2段階の冷却条件を採用する
時、この段階まで未変態のまま残っていた残留γ相にも
変化が生じる。この変化は変態の進行に伴って排出され
たCが残留γ相に濃化する現象である。この現象によっ
て次の第3段階以降で起こる残留γ相の低温変態相への
変態が影響を受け、C濃化が少ない場合には低温変態相
はパーライトやベイナイトとなり易く、多い場合にはマ
ルテンサイトや残留γのまま残存し易くなる。高強度の
熱延鋼板を得るにはC濃化を進めてより低温の変態第2
相を生成させることが有効となる。このような効果も含
めて第2段階の緩冷却期問のもっとも望ましい条件は7
秒以上とするのがよい。本発明での制御冷却の大きな特
徴点はこの第2段階の緩冷却区問を採用することにあ
り、本発明の要件を満たすことによってフェライト粒を
極微細化させる効果と、フェライト体積率を高める効果
と、強度を高める効果とを同時に達成させることができ
るのである。
When the cooling conditions of the second stage are adopted, the residual γ phase which remains untransformed up to this stage also changes. This change is a phenomenon in which C discharged along with the transformation is concentrated in the residual γ phase. This phenomenon affects the transformation of the residual γ phase to the low temperature transformation phase that occurs in the third and subsequent steps, and when the C concentration is low, the low temperature transformation phase is likely to be pearlite or bainite, and when it is high, it is martensite. And the residual γ tends to remain. To obtain high-strength hot-rolled steel sheet, the concentration of C should be advanced and the lower temperature transformation
It is effective to generate a phase. Including such effects, the most desirable condition for the second stage slow cooling period is 7
It is better to be more than a second. A major feature of the controlled cooling in the present invention is that the slow cooling section of the second stage is adopted. By satisfying the requirements of the present invention, the effect of making the ferrite grains extremely fine and the ferrite volume ratio are increased. The effect and the effect of increasing the strength can be achieved at the same time.

【0031】第3段階の冷却では、20℃/sec 以上の
速度で550℃以下の温度範囲まで冷却を行う。この冷
却における要件は残留γ相をパーライト、べイナイト、
マルテンサイトなどの低温変態相に変態させたり、ある
いは残留γのまま最終まで残存させるなどの、目的に応
じた好ましい第2相を形成する上で必要な条件である。
第2相を、これらの低温変態相のうちのいずれにするか
は、主にどの程度の強度、加工性あるいは靱性を得たい
かによって選択することになるが、この調整は次に述べ
る巻取り温度によって行うのがよい。しかし、この区間
での冷却速度が20℃/sec 未満であったり、冷却停止
温度が550℃を超えて高くなった場台には、低温変態
相はパーライト主体の組織にしかならず、より高強度化
を図るためにベイナイトやマルテンサイトを狙って巻き
取り温度を低下させてもその狙いがかなわなくなる。冷
却速度の下限を20℃/sec 、冷却停止温度の上限を5
50℃と定めるのは以上の理由による。
In the third stage of cooling, cooling is performed at a rate of 20 ° C./sec or more to a temperature range of 550 ° C. or less. The requirement for this cooling is to remove residual γ phase from pearlite, bainite,
It is a necessary condition for forming a preferable second phase according to the purpose, such as transformation into a low temperature transformation phase such as martensite, or remaining until the end with residual γ.
Which of these low temperature transformation phases is used for the second phase is mainly selected depending on how much strength, workability or toughness is desired. It is better done by temperature. However, when the cooling rate in this section is less than 20 ° C / sec or the cooling stop temperature exceeds 550 ° C and becomes high, the low-temperature transformation phase has only a pearlite-based structure, resulting in higher strength. Even if the winding temperature is lowered to aim at bainite or martensite in order to achieve this, the aim cannot be achieved. The lower limit of cooling rate is 20 ° C / sec and the upper limit of cooling stop temperature is 5
The reason why the temperature is set to 50 ° C. is as described above.

【0032】・巻き取り条件 上述したように、巻き取りの温度を所定の範囲で制御す
れば、強度、延性、靭性の目標レベルに応じて、第2相
をパーライト、ベイナイト、マルテンサイト、残留γな
どの組織に調整することができる。例えば、比較的強度
を抑えて延性を高めたい場合には、巻き取り温度を高め
に設定して第2相をパーライト主体の組織にし、また、
高い強度でかつ低降伏比の材質特性を得たい場台には、
巻き取り温度を低めに設定して第2相をマルテンサイト
主体の組織にすることが可能である。しかし、巻き取り
温度が550℃を超えると、第2相をマルテンサイトと
することができなくなり、材質を調整する自由度が小さ
くなること、また、巻き取り後の自己焼鈍効果が大きく
なって極微細化させたフェライト粒が粒成長を起こすな
ど好ましくない結果を招く。したがって、巻き取り温度
の上限は550℃とする。なお、望ましい巻き取り温度
の範囲は400〜530℃である。
Winding Conditions As described above, if the winding temperature is controlled within a predetermined range, the second phase is pearlite, bainite, martensite, residual γ depending on the target level of strength, ductility and toughness. Etc. can be adjusted to the organization. For example, when it is desired to suppress the strength relatively and increase the ductility, the winding temperature is set to be high and the second phase has a structure mainly composed of pearlite.
For a platform that requires high strength and low yield ratio material properties,
It is possible to set the winding temperature to a low temperature and make the second phase a structure mainly composed of martensite. However, when the winding temperature exceeds 550 ° C., the second phase cannot be made into martensite, the degree of freedom in adjusting the material becomes small, and the self-annealing effect after winding becomes large, resulting in an extremely high temperature. This causes unfavorable results such as grain growth of finely divided ferrite grains. Therefore, the upper limit of the winding temperature is 550 ° C. The desirable winding temperature range is 400 to 530 ° C.

【0033】[0033]

【実施例】次に実施例によって本発明をさらに具体的に
説明する。表1に示す化学成分の鋼を溶製し、表2、表
3に示す条件で熱間圧延および冷却を行い、3.0mm
厚さの熱延鋼板を製造し、酸洗した後ポリゴナルフェラ
イト体積率、フェライト結晶粒径を測定するとともに、
JIS5号試験片による引張り特性、両振り曲げ試験法
による疲労特性、原厚まま2mmVノッチシャルピー試
験片による延性一脆性遷移温度を調査した。なお、表
2、表3におけるにおける20%圧下以上のパス数と
は、1パス当たりの圧下率を20%以上としたパス数の
累計である。いずれのパスでも1パス当たりの圧下率の
上限は40%未満とした。これらの調査結果を表4、表
5に示す。
Next, the present invention will be described more specifically with reference to examples. Steel having the chemical composition shown in Table 1 was melted, hot-rolled and cooled under the conditions shown in Tables 2 and 3, and 3.0 mm
A hot-rolled steel sheet having a thickness is manufactured, and after being pickled, the polygonal ferrite volume ratio and the ferrite crystal grain size are measured,
Tensile properties by JIS No. 5 test piece, fatigue properties by both-way bending test method, and ductile-brittle transition temperature by 2 mm V notch Charpy test piece with the original thickness were investigated. The number of passes of 20% reduction or more in Tables 2 and 3 is the total number of passes with a reduction rate of 20% or more per pass. In any of the passes, the upper limit of the rolling reduction per pass was less than 40%. The results of these investigations are shown in Tables 4 and 5.

【0034】[0034]

【表1】 [Table 1]

【0035】[0035]

【表2】 [Table 2]

【0036】[0036]

【表3】 [Table 3]

【0037】[0037]

【表4】 [Table 4]

【0038】[0038]

【表5】 [Table 5]

【0039】表4、表5の結果をもとに、まず、ポリゴ
ナルフェライト体積率およびフェライト結晶粒径が機械
的性質に対してどのような影響を示すかについて述べ
る。図1および図2は、得られたデータから、それぞれ
ポリゴナルフェライト体積率またはフェライト結晶粒径
とTS×El、耐久比(FL/TS)、 vTrsとの関係
をプロットしたものである。
Based on the results of Tables 4 and 5, first, how the volume fraction of polygonal ferrite and the ferrite crystal grain size have an influence on the mechanical properties will be described. 1 and 2 are plots of the relationship between polygonal ferrite volume ratio or ferrite crystal grain size and TS × El, durability ratio (FL / TS), and vTrs based on the obtained data.

【0040】これらの図から明かなように、発明法に従
う熱延鋼板はいずれも、ポリゴナルフェライト体積率が
80%以上、かつ、フェライト結晶粒径が10μm未満
であり、比較例よりもTS×El、耐久比、 vTrsの値
が優れていることがわかる。これに対して、比較例では
ポリゴナルフェライト体積率が80%未満、フェライト
結晶粒径が10μm以上のものが大部分であり、一部N
o. 1、No. 27、No.29のようにポリゴナルフェライ
ト体積率が80%以上のもの、No. 12、No.31のよ
うにフェライト結晶粒径が10μm未満のものが含まれ
るが、前者のグループのものはフェライト結晶粒径が1
0μm以上、また後者のグループのものはポリゴナルフ
ェライト体積率が80%未満である。
As is clear from these figures, all of the hot-rolled steel sheets according to the method of the present invention have a volume ratio of polygonal ferrite of 80% or more and a ferrite crystal grain size of less than 10 μm, and TS × is larger than that of the comparative example. It can be seen that the values of El, durability ratio, and vTrs are excellent. On the other hand, in the comparative example, most of the polygonal ferrite has a volume ratio of less than 80% and a ferrite crystal grain size of 10 μm or more.
o. No. 1, No. 27 and No. 29 with a polygonal ferrite volume ratio of 80% or more, and No. 12, No. 31 with a ferrite crystal grain size of less than 10 μm are included. The former group has a ferrite grain size of 1
The volume fraction of polygonal ferrite of the latter group is 0% or more and less than 80%.

【0041】これらのことは、ポリゴナルフェライト体
積率とフェライト結晶粒径のいずれか一方だけを本発明
の範囲に調整し得たとしても良好な機械的性質を得るこ
とができず、両者の条件が同時に本発明の範囲を満足し
てはじめて良好な特性が得られることを示している。
These facts indicate that even if only one of the polygonal ferrite volume ratio and the ferrite crystal grain size can be adjusted within the range of the present invention, good mechanical properties cannot be obtained, and both conditions are satisfied. At the same time, it shows that good characteristics can be obtained only when the range of the present invention is satisfied.

【0042】[0042]

【発明の効果】以上説明したように、本発明に従う製造
方法によれば、ポリゴナルフェライト体積率とフェライ
ト結晶粒径を同時に調整でき、これにより延性、靭性、
疲労強度を格段に高めることが可能となる。また、本発
明に従う製造方法によれば、ポリゴナルフェライト体積
率が高いので、機械的性質の異方性が少なく、しかも、
一般のホットストリップミルで容易に実施することが可
能であるので、産業上の寄与は極めて大きい。
As described above, according to the manufacturing method of the present invention, the volume ratio of polygonal ferrite and the grain size of ferrite can be adjusted at the same time, whereby ductility, toughness, and
Fatigue strength can be remarkably increased. Further, according to the manufacturing method according to the present invention, since the volume ratio of polygonal ferrite is high, the anisotropy of mechanical properties is small, and
Since it can be easily carried out by a general hot strip mill, the industrial contribution is extremely large.

【図面の簡単な説明】[Brief description of the drawings]

【図1】フェライト結晶粒径と機械的性質との関係を示
すグラフである。
FIG. 1 is a graph showing the relationship between ferrite crystal grain size and mechanical properties.

【図2】ポリゴナルフェライト体積率と機械的性質との
関係を示すグラフである。
FIG. 2 is a graph showing the relationship between polygonal ferrite volume ratio and mechanical properties.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C22C 38/58 C22C 38/58 (72)発明者 山崎 義男 千葉県千葉市中央区川崎町1番地 川崎製 鉄株式会社技術研究所内 (72)発明者 小林 崇 千葉県千葉市中央区川崎町1番地 川崎製 鉄株式会社技術研究所内 (72)発明者 加藤 俊之 千葉県千葉市中央区川崎町1番地 川崎製 鉄株式会社技術研究所内─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification number Reference number within the agency FI Technical indication C22C 38/58 C22C 38/58 (72) Inventor Yoshio Yamazaki 1 Kawasaki-cho, Chuo-ku, Chiba-shi, Chiba Kawasaki Steel Co., Ltd. Technical Research Institute (72) Inventor Takashi Kobayashi 1 Kawasaki-cho, Chuo-ku, Chiba City, Chiba Prefecture Kawasaki Steel Co., Ltd. Technical Research Lab. Kawasaki Steel Corporation Technical Research Center

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】C:0.05〜 0.30 wt%、 Si:2.0 wt%以下、 Mn:1.0 〜2.5 wt%、 Al:0.05wt%以下、を含み、かつTi:0.05〜0.3 wt%、 Nb:0.10wt%以下、のうちの1種または2種を含有し、
残部がFeおよび不可避的不純物よりなる鋼を、950〜
1100℃の温度に加熱した後、1回当りの圧下量が2
0%以上となる圧下を少なくとも2回以上加え、仕上げ
温度がAr3変態点以上になるように熱間圧延し、Ar3
態点〜750℃の温度範囲を20℃/sec 以上の速度で
冷却し、続いて750℃未満〜600℃の温度範囲にお
いて、5〜20sec の時間滞留させた後、再び20℃/
sec 以上の速度で550℃以下の温度まで冷却し、55
0℃以下の温度でコイルに巻取ることを特徴とするフェ
ライト体積率が80%以上で、平均フェライト粒径が1
0μm未満の極微細組織を有する高張力熱延鋼板の製造
方法。
1. C: 0.05 to 0.30 wt%, Si: 2.0 wt% or less, Mn: 1.0 to 2.5 wt%, Al: 0.05 wt% or less, and Ti: 0.05 to 0.3 wt%, Nb: 0.10. wt% or less, containing one or two of
A steel whose balance is Fe and unavoidable impurities is
After heating to a temperature of 1100 ° C, the reduction amount per operation is 2
A reduction of 0% or more is applied at least twice, hot rolling is performed so that the finishing temperature is the Ar 3 transformation point or more, and the temperature range from the Ar 3 transformation point to 750 ° C is cooled at a rate of 20 ° C / sec or more. Then, in the temperature range of less than 750 ° C to 600 ° C, the resin is allowed to stay for 5 to 20 seconds, and then again at 20 ° C /
Cool to a temperature of 550 ° C or less at a speed of sec or more, and
The ferrite volume ratio is 80% or more and the average ferrite grain size is 1 which is characterized by being wound around a coil at a temperature of 0 ° C or less.
A method for producing a high-strength hot-rolled steel sheet having an ultrafine structure of less than 0 μm.
【請求項2】C:0.05〜 0.30 wt%、 Si:2.0 wt%以下、 Mn:1.0 〜2.5 wt%、 Al:0.05wt%以下、を含み、かつTi:0.05〜0.3 wt%、 Nb:0.10wt%以下、のうちの1種または2種を含有し、
さらにCr:1.5 wt%以下、 Cu:1.5 wt%以下、 Ni:1.5 wt%以下、 Mo:1.5 wt%以下から選ばれる1種または2種以上を含
有し、残部がFeおよび不可避的不純物よりなる鋼を、9
50〜1100℃の温度に加熱した後、1回当りの圧下
量が20%以上となる圧下を少なくとも2回以上加え、
仕上げ温度がAr3変態点以上になるように熱間圧延し、
Ar3変態点〜750℃の温度範囲を20℃/sec 以上の
速度で冷却し、続いて750℃未満〜600℃の温度範
囲において、5〜20sec の時間滞留させた後、再び2
0℃/sec 以上の速度で550℃以下の温度まで冷却
し、550℃以下の温度でコイルに巻取ることを特徴と
するフェライト体積率が80%以上で、平均フェライト
粒径が10μm未満の極微細組織を有する高張力熱延鋼
板の製造方法。
2. C: 0.05 to 0.30 wt%, Si: 2.0 wt% or less, Mn: 1.0 to 2.5 wt%, Al: 0.05 wt% or less, and Ti: 0.05 to 0.3 wt%, Nb: 0.10. wt% or less, containing one or two of
Further, it contains one or more selected from Cr: 1.5 wt% or less, Cu: 1.5 wt% or less, Ni: 1.5 wt% or less, Mo: 1.5 wt% or less, and the balance is Fe and inevitable impurities. Steel, 9
After heating to a temperature of 50 to 1100 ° C., a reduction amount of 20% or more per time is added at least twice,
Hot rolling so that the finishing temperature is above the Ar 3 transformation point,
After cooling in the temperature range of Ar 3 transformation point to 750 ° C. at a rate of 20 ° C./sec or more, and then allowing it to stay for 5 to 20 sec in the temperature range of less than 750 ° C. to 600 ° C.
A pole having a ferrite volume ratio of 80% or more and an average ferrite grain size of less than 10 μm, characterized by being cooled to a temperature of 550 ° C. or lower at a rate of 0 ° C./sec or more and being wound around a coil at a temperature of 550 ° C. or less. A method for producing a high-strength hot-rolled steel sheet having a fine structure.
JP30026295A 1995-11-17 1995-11-17 Method for producing high-strength hot-rolled steel sheet having ultrafine structure Expired - Fee Related JP3477955B2 (en)

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