KR100554753B1 - High strength cold rolled steel sheet with superior formability and weldability and method for manufacturing thereof - Google Patents

High strength cold rolled steel sheet with superior formability and weldability and method for manufacturing thereof Download PDF

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KR100554753B1
KR100554753B1 KR1020010085539A KR20010085539A KR100554753B1 KR 100554753 B1 KR100554753 B1 KR 100554753B1 KR 1020010085539 A KR1020010085539 A KR 1020010085539A KR 20010085539 A KR20010085539 A KR 20010085539A KR 100554753 B1 KR100554753 B1 KR 100554753B1
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steel sheet
weldability
rolled steel
temperature
cold rolled
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KR20030055524A (en
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백승철
배춘선
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주식회사 포스코
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Priority to US10/481,354 priority patent/US20040238083A1/en
Priority to JP2003556557A priority patent/JP3895728B2/en
Priority to EP02741471A priority patent/EP1458896A4/en
Priority to PCT/KR2002/001167 priority patent/WO2003056041A1/en
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    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/18Hardening; Quenching with or without subsequent tempering
    • C21D1/19Hardening; Quenching with or without subsequent tempering by interrupted quenching
    • C21D1/20Isothermal quenching, e.g. bainitic hardening
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0273Final recrystallisation annealing
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    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
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    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
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    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/001Austenite
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    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/002Bainite
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    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226Hot rolling
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    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0236Cold rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0278Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips involving a particular surface treatment

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Abstract

본 발명은 자동차용 구조용 부품으로 사용되었을 때 쉽게 성형이 되면서 자동차의 충돌시 에너지 흡수성이 우수하여 자동차의 안정성을 향상시킬 수 있는 인장강도 70~90kgf/mm2급 고강도 냉연강판과 그 제조방법에 관한 것이다. The present invention relates to a tensile strength 70 ~ 90kgf / mm grade 2 high strength cold rolled steel sheet and a method of manufacturing the same which can be easily molded when used as a structural part for automobiles to improve the stability of the vehicle due to the excellent energy absorption in the collision of the vehicle will be.

본 발명은 중량%로, C: 0.15~0.25 %, Si: 0.5~1.2%, Mn: 1.0~2.0 %, P: 0.25 % 이하, S: 0.020%이하, Al: 0.015 ~ 0.050%, N: 0.008 ~0.026%, 상기 Si와 P가 다음의 관계, 1.5 ≤ Si[%] + 50/8 P[%] ≤2.0를 만족하고 나머지 Fe와 불가피한 불순물로 조성되는 성형성 및 용접성이 우수한 고강도 냉연강판과, The present invention is in weight%, C: 0.15 to 0.25%, Si: 0.5 to 1.2%, Mn: 1.0 to 2.0%, P: 0.25% or less, S: 0.020% or less, Al: 0.015 to 0.050%, N: 0.008 ~ 0.026%, the high strength cold rolled steel sheet having excellent formability and weldability, wherein the Si and P satisfy the following relationship, 1.5 ≦ Si [%] + 50/8 P [%] ≦ 2.0 and are composed of the remaining Fe and unavoidable impurities; ,

이 냉연강판을 아래 관계식 2의 범위의 온도에서 50sec이상 연속소둔하는 단계,  Continuously annealing the cold rolled steel sheet at a temperature in the range of relation 2 below 50 sec,

[관계식 2][Relationship 2]

563 + 651 C[%] + 42 Si[%] + 18 Mn[%] < 소둔온도 [℃] ≤ 850℃563 + 651 C [%] + 42 Si [%] + 18 Mn [%] <Annealing Temperature [℃] ≤ 850 ℃

상기 연속소둔하고 20~100℃/sec 냉각속도로 오스템퍼링 개시온도 400~450℃ 까지 급랭한 후 350~400℃까지 200~500sec 동안에 냉각하는 오스템퍼링하는 단계를 포함하여 이루어지는 성형성 및 용접성이 우수한 고강도 냉연강판의 제조방법에 관한 것을 그 기술요지로 한다. Excellent continuous formability and weldability comprising the step of continuous annealing and quenching the ostempering start temperature 400 ~ 450 ℃ at a cooling rate of 20 ~ 100 ℃ / sec and then cooling to 200 ~ 500 sec to 350 ~ 400 ℃ The technical subject matter of the manufacturing method of a high strength cold-rolled steel sheet is made.

가공유기변태강, 자동차부품, 잔류오스테나이트, 용접성, 성형성Machining organic transformation steel, automotive parts, residual austenite, weldability, formability

Description

성형성 및 용접성이 우수한 고강도 냉연강판과 그 제조방법{High strength cold rolled steel sheet with superior formability and weldability and method for manufacturing thereof}High strength cold rolled steel sheet with superior formability and weldability and method for manufacturing manufacture

도 1은 C-1.5Mn-1.5Si 강과 C-1.5Mn-1.0Si-0.08P강의 상태도가 동일함을 보여주는 그래프1 is a graph showing that the state diagrams of C-1.5Mn-1.5Si steel and C-1.5Mn-1.0Si-0.08P steel are the same.

도 2는 AlN의 석출물이 오스테나이트 성장을 억제하는 것을 보여주는 미세조직사진Figure 2 is a microstructure photograph showing that the precipitate of AlN inhibits austenite growth

도 3은 각 C, Si, Mn 함량을 함유한 강의 소둔온도에 따른 오스테나이트 분율을 비교한 그래프3 is a graph comparing austenite fractions according to annealing temperatures of steels containing C, Si, and Mn contents, respectively;

본 발명은 자동차용 구조용 부품으로 사용되었을 때 쉽게 성형이 되면서 자동차의 충돌시 에너지 흡수성이 우수하여 자동차의 안정성을 향상시킬 수 있는 인장강도 70~90kgf/mm2급 고강도 냉연강판과 그 제조방법에 관한 것이다. The present invention relates to a tensile strength 70 ~ 90kgf / mm grade 2 high strength cold rolled steel sheet and a method of manufacturing the same which can be easily molded when used as a structural part for automobiles to improve the stability of the vehicle due to the excellent energy absorption in the collision of the vehicle will be.

최근 들어 환경이 사회적으로 중요한 문제로 부각되면서 세계적으로 자동차 배기가스 및 연비의 규제가 강화되고 있다. 또한 충돌 안정성에 대한 규제도 계속 강화되고 있으므로 이에 대응하여 세계 각국의 자동차 제조사는 가벼우면서 충돌 안전성이 우수한 자동차를 개발하고 있다. 또한 자동차의 증가와 함께 자동차 사고의 빈도가 높아지면서 승객의 안전이 강조되고 있다. 자동차를 가볍게 만들면서 충돌 안전성을 향상시키기 위하여는 강도가 높은 재료를 사용하여 자동차를 제조하여야 한다.Recently, as the environment has emerged as a socially important issue, regulations on automobile emissions and fuel economy have been tightened worldwide. In addition, as regulations on collision stability continue to be tightened, automobile manufacturers around the world are developing vehicles that are light and have excellent collision safety. In addition, as the number of automobiles increases with the increase of automobiles, the safety of passengers is emphasized. In order to make the vehicle lighter and improve crash safety, automobiles must be manufactured using materials of high strength.

자동차 충돌 안정성에 대한 규제가 강화되면서 기존의 정면충돌, 측면충돌의 평가와 함께 기존 정면충돌 대비 엄격한 기준인 오프세트 충돌 평가시험을 추가되었다. 자동차 안정성에 있어서 범퍼의 에너지 흡수성이 중요하며 범퍼의 에너지 흡수성을 높이기 위하여 자동차 부품 재료의 강도를 증가시키고 있다. As regulations on automobile collision stability are tightened, the evaluation of existing frontal and side collisions is added, and an offset collision evaluation test, which is a stricter standard compared to the existing frontal collisions, has been added. The energy absorption of the bumper is important in automobile stability, and the strength of the automotive part material is increased to increase the energy absorption of the bumper.

종래의 고강도 냉연강판의 제조기술은 [1]가공경화강, [2]복합조직강, [3]가공유기변태강으로 구분할 수 있다. Conventional manufacturing techniques of high strength cold rolled steel sheet can be divided into [1] processing hardened steel, [2] composite steel, and [3] common steel transformation steel.

[1] 가공경화강[1] hardened steels

냉간압연에 의한 가공경화를 이용하는 방법으로 냉간압연 후 회복소둔을 실시하여 미재결정조직으로 강도를 증가시키므로 첨가 합금의 양이 적고 용접성이 우수하다는 장점이 있다. 그러나 연신율이 낮으므로 성형성이 나쁘다. As a method using work hardening by cold rolling, the recovery annealing is performed after cold rolling to increase the strength of the recrystallized structure, so the amount of the additive alloy is small and the weldability is excellent. However, since elongation is low, moldability is bad.

[2]복합조직강[2] composite tissue steels

냉간압연 후 소둔온도를 A1 변태점 이상으로 가열하여 오스테나이트를 형성한 후 급랭하여 오스테나이트를 마르텐사이트나 베이나이트로 변태시켜서 재료의 강도를 증가시키는 복합조직강이 있다. 이러한 강은 열처리 공정에서 냉각속도가 빨라야 하므로 제조가 어렵고 연신율이 낮은 단점이 있다. After cold rolling, the annealing temperature is heated above the A 1 transformation point to form austenite, followed by quenching to transform austenite into martensite or bainite, thereby increasing the strength of the material. These steels are difficult to manufacture and have a low elongation rate because the cooling rate must be high in the heat treatment process.

[3]가공유기변태강[3] sharing slots

잔류 오스테나이트를 강중에 존재시켜 연신율을 증가시키는 가공유기변태강이 있다. 성형 중에 잔류 오스테나이트가 높은 강도의 마르텐사이트로 변태하면서 가공경화속도가 빨라져서 연신율이 증가하는 것이다. 가공유기변태강에 잔류 오스테나이트를 포함한 강으로 기본 첨가원소는 C, Si, 및 Mn으로 알려져 있다. C은 마르텐사이트의 변태온도를 감소시켜 오스테나이트를 안정하게 하고 Si은 탄화물의 형성을 억제하여 잔류 오스테나이트 내의 고용 C 함량을 증가시키는 역할을 한다. Mn은 C과 함께 마르텐사이트 변태 온도를 하향하고 강도를 증가시키는 역할을 한다. There is a processed organic transformation steel which increases the elongation by remaining residual austenite in the steel. As the retained austenite is transformed into high strength martensite during molding, the elongation is increased due to the faster work hardening rate. It is a steel containing residual austenite in processed organic transformation steel, and its basic additive elements are known as C, Si, and Mn. C reduces the transformation temperature of martensite to stabilize austenite and Si inhibits the formation of carbides to increase the solid solution C content in the retained austenite. Mn, together with C, serves to lower the martensite transformation temperature and increase strength.

가공유기변태강을 자동차의 구조부품으로 적용하여 경량화하기 위해서는 단순 C-Si-Mn 계의 가공유기변태강 보다 성형성이 증가되어야 한다. 더욱이 자동차의 형상이 복잡하여 지면서 기존의 성형성 강은 많은 수의 자동차 부품에 적용되지 못하고 있다. 이러한 문제점을 해결하기 위하여는 성형성이 향상된 가공유기변태강이 제조되어야 한다. 성형성과 함께 향상되어야 할 성질이 용접성이다. 기존의 가공유기변태강에서는 탄화물의 형성을 억제하고 잔류 오스테나이트의 분율을 증가시켜 성형성을 형성시키기 위하여 Si이 1.5%이상 함유되어 있다. Si 함량이 높으면 용접성이 열화되어 강판의 생산 시 강판과 강판을 용접하는 과정에서 불량의 발생률이 높을 뿐 아니라 이러한 강판으로 자동차 부품을 제작하고 점용접으로 부품을 제작할 경우 용접 불량이 생긴다. In order to reduce the weight by applying the processed organic transformation steel to structural parts of automobiles, the formability should be increased than the processing organic transformation steel of the simple C-Si-Mn system. Moreover, as the shape of automobiles becomes more complex, conventional formability steels are not applied to a large number of automobile parts. In order to solve this problem, processed organic transformation steel with improved formability should be manufactured. The property to be improved along with formability is weldability. In the conventional processing organic transformation steel, Si is contained in an amount of 1.5% or more to suppress the formation of carbides and increase the fraction of retained austenite to form formability. If the Si content is high, the weldability is deteriorated, and not only the incidence of defects in the process of welding the steel sheet and the steel sheet during the production of the steel sheet is high, but also the welding defects are produced when the automobile parts are manufactured from such steel sheets and the parts are manufactured by spot welding.

본 발명은 종래의 가공유기변태강의 특성을 개선하기 위하여 안출된 것으로서, 성형성이 우수하며 강도가 높기 때문에 자동차 구조용 부품으로 사용되었을 때 부품 재료의 두께를 감소시켜 자동차를 경량화 시키며 자동차의 충돌시 에너지 흡수성이 우수하여 자동차의 안정성을 향상시킬 수 있는 성형성과 동시에 용접성도 우수한 인장강도 70~90kgf/mm2급 냉연강판을 제공하는데, 그 목적이 있다. The present invention was devised to improve the characteristics of conventional processed organic transformation steel, and because of its excellent formability and high strength, it is possible to reduce the thickness of parts materials when used as structural parts for automobiles, thereby reducing the weight of automobiles and energy during collision of automobiles. It is an object of the present invention to provide a tensile strength of 70 ~ 90kgf / mm grade 2 cold rolled steel sheet excellent in moldability and weldability at the same time to improve the stability of the vehicle with excellent absorption.

상기 목적을 달성하기 위한 본 발명의 냉연강판은, 중량%로, C: 0.15~0.25 %, Si: 0.5~1.2%, Mn: 1.0~2.0 %, P: 0.25 % 이하, S: 0.020%이하, Al: 0.015 ~ 0.050%, N: 0.008 ~0.026%, 상기 Si와 P가 다음의 관계, 1.5 ≤ Si[%] + 50/8 P[%] ≤2.0를 만족하고 나머지 Fe와 불가피한 불순물로 조성된다. Cold rolled steel sheet of the present invention for achieving the above object, in weight%, C: 0.15-0.25%, Si: 0.5-1.2%, Mn: 1.0-2.0%, P: 0.25% or less, S: 0.020% or less, Al: 0.015 to 0.050%, N: 0.008 to 0.026%, wherein Si and P satisfy the following relationship, 1.5 ≦ Si [%] + 50/8 P [%] ≦ 2.0 and are composed of the remaining Fe and unavoidable impurities .

또한, 본 발명의 냉연강판 제조방법은, In addition, the cold rolled steel sheet manufacturing method of the present invention,

상기와 같이 조성되는 냉연강판을 아래 관계식 2의 범위의 온도에서 50sec이상 연속소둔하는 단계, Continuously annealing the cold rolled steel sheet formed as described above at a temperature in the range of relation 2 below 50 sec,

[관계식 2][Relationship 2]

563 + 651 C[%] + 42 Si[%] + 18 Mn[%] < 소둔온도 [℃] ≤ 850℃563 + 651 C [%] + 42 Si [%] + 18 Mn [%] <Annealing Temperature [℃] ≤ 850 ℃

상기 연속소둔하고 20~100℃/s 냉각속도로 오스템퍼링 개시온도 400~450℃ 까지 급랭한 후 350~400℃까지 200~500s 동안에 냉각하는 오스템퍼링하는 단계를 포함하여 구성된다. The continuous annealing and quenching at 20 ~ 100 ℃ / s cooling rate to the ostempering start temperature 400 ~ 450 ℃ and then comprises a step of osstem cooling to 200 ~ 500 s to 350 ~ 400 ℃.

이하 본 발명에 대하여 상세히 설명한다. Hereinafter, the present invention will be described in detail.

본 발명은 강에 적정한 함량의 C, Si, P, Mn을 첨가하여 적정한 양의 잔류오스테나이트를 형성함으로 높은 연신율을 유지하면서 적정한 양의 Al과 N의 첨가로 AlN을 석출시켜서 결정립을 미세화하여 강도를 증가시켜 우수한 성형성 및 용접성을 갖는 자동차 구조용 부품에 적합한 고강도 냉연강판을 연속소둔법으로 제조하는데 특징이 있다. 이러한 본 발명을 강조성범위와 그 제조조건으로 구분하여 설명한다. The present invention forms an appropriate amount of residual austenite by adding an appropriate amount of C, Si, P, and Mn to the steel, while maintaining a high elongation, by depositing AlN with the addition of an appropriate amount of Al and N to refine the grain size It is characterized by the production of a high strength cold rolled steel sheet suitable for automotive structural parts having excellent formability and weldability by the continuous annealing method. The present invention will be described by dividing it into emphasis range and manufacturing conditions thereof.

[강 조성범위][Range composition range]

·C:0.15~0.25% · C: 0.15 ~ 0.25%

C은 마르텐사이트 변태온도를 낮추어 오스테나이트를 안정하여 상온에서 잔류오스테나이트가 형성되어 연신율을 증가시키는 성분으로, 0.1%이상 첨가되어야 안정한 잔류오스테나이트를 얻을 수 있으나, 0.25% 초과의 경우에는 용접성이 열화되어 냉연강판 제조시 강판의 용접 및 자동차 부품의 용접 공정에 불리하다.C is a component that stabilizes austenite by lowering the martensite transformation temperature to form residual austenite at room temperature, thereby increasing elongation, and it is necessary to add 0.1% or more to obtain stable residual austenite. It is deteriorated, which is disadvantageous for welding of steel sheets and welding of automobile parts in the production of cold rolled steel sheets.

· Si:0.5~1.2% · Si: 0.5 ~ 1.2%

Si은 오스템퍼링 과정에서 탄화물 형성을 억제하는 역할을 한다. Si에 의해 탄화 물 형성이 억제되면 고용 C의 양이 증가되어 많은 고용 C이 잔류 오스테나이트로 확산되므로 잔류 오스테나이트가 안정화된다. 반면 Si은 용접성을 급격히 감소시키므로 냉연공정중 용접과 자동차 부품으로 성형후의 용접을 원활하게 하기 위하여 Si의 함량이 적은 게 좋다. 즉, 우수한 성형성을 위하여 적정한 분율의 잔류 오스테나이트를 만들기 위하여는 Si 함량이 많아야 하며 용접성을 위하여는 Si 함량이 적어야 한다. 따라서, 본 발명에서는 탄화물 형성의 억제를 효과적으로 하기 위해 Si을 0.5%이상 첨가하면서 용접성을 고려하여 1.2%이하로 제하는 것이 바람직하다. 이와 같이 Si의 함량을 1.2% 이하로 억제하여 용접성을 향상시키면서 Si과 함께 첨가되었을 때 탄화물 형성을 억제 시켜주는 P를 동시에 첨가하여 잔류 오스테나이트의 분율을 유지하는 것이다. P가 첨가되지 않으면 탄화물 형성을 억제하고 잔류 오스테나이트를 적당량 형성시키기 위하여는 Si은 1.5 ~ 2.0% 함유시켜야 하지만 P를 동시에 첨가하면 Si을 0.5 ~1.2%로 첨가하여도 1.5~2.0% 첨가한 효과를 얻을 수 있다. Si plays a role in suppressing carbide formation in the ostempering process. When the formation of carbides by Si is suppressed, the amount of solid solution C is increased, so that a large amount of solid solution C diffuses into the residual austenite, so that the residual austenite is stabilized. On the other hand, since Si drastically reduces the weldability, it is preferable that the Si content is small in order to facilitate the welding during the cold rolling process and the welding after molding into automotive parts. That is, in order to make an appropriate fraction of retained austenite for good moldability, the Si content should be high and the Si content should be low for weldability. Therefore, in the present invention, in order to effectively suppress the formation of carbides, it is preferable to reduce the content to 1.2% or less in consideration of weldability while adding 0.5% or more of Si. In this way, while suppressing the content of Si to 1.2% or less while improving the weldability, simultaneously adding P, which suppresses carbide formation when added with Si, maintains the fraction of retained austenite. If P is not added, Si should be contained 1.5 to 2.0% in order to suppress carbide formation and to form a proper amount of retained austenite.However, when P is added at the same time, 1.5 to 2.0% is added even if Si is added at 0.5 to 1.2%. Can be obtained.

· Mn: 1.0~2.0% · Mn: 1.0 ~ 2.0%

Mn은 재료의 강도를 증가시키며 C과 같이 마르텐사이트의 변태온도를 감소시켜 오스테나이트를 안정화시킨다. Mn을 1.0% 미만 첨가하면 강도가 낮아지고 잔류 오스테나이트가 불안정하여 진다. 또한 Mn을 2.0% 보다 많이 첨가하면 페라이트의 변태속도가 너무 느려지므로 냉각 중에 형성되는 페라이트가 적어진다. 페라이트가 많이 형성되면 많은 양의 고용 C이 잔류 오스테나이트로 확산되어 들어가서 잔류 오스테나이트가 안정화되는 것이므로 적당한 양의 페라이트를 형성하는 것이 중요하다. Mn의 과도한 양의 첨가하면 냉각 중 페라이트로 변태하지 못한 오스테나이트가 오스템퍼링온도에서 높은 분율의 베이나이트가 형성되어 강도가 증가하면서 연신율이 감소한다. 본 발명에서는 이러한 점을 고려하여 Mn의 함량을 1.0~2.0 %로 제한하는 것이다. Mn increases the strength of the material and stabilizes austenite by decreasing the transformation temperature of martensite, such as C. If Mn is added less than 1.0%, the strength is lowered and the residual austenite becomes unstable. In addition, when Mn is added more than 2.0%, the transformation rate of the ferrite becomes too slow, so that the ferrite formed during the cooling decreases. When a large amount of ferrite is formed, it is important to form an appropriate amount of ferrite because a large amount of solid solution C diffuses into the residual austenite and the residual austenite is stabilized. The addition of excessive amounts of Mn leads to the formation of a high fraction of bainite at austempering temperatures at the austenite, which does not transform into ferrite during cooling, increasing the strength and decreasing the elongation. In the present invention, in consideration of this point, the content of Mn is limited to 1.0 to 2.0%.

· P:0.25%이하 · P: 0.25% or less

P는 Si과 같은 페라이트 강화원소로 탄화물 형성을 효과적으로 억제하기 위해 첨가하는데, 그 함량이 0.25% 초과의 경우 슬라브를 제조하는 과정에서 결정립의 중심부에 P가 너무 많이 편석하여 연속주조 과정에서 파단이 일어날 가능성이 높아진다. 또한 제품의 결정립계에 많은 양의 P가 편석되어 결정립계 파괴로 인한 강성이 감소할 수 있다. P is added to ferrite strengthening elements such as Si to effectively suppress the formation of carbides. If the content is more than 0.25%, P is segregated too much in the center of crystal grains during the slab manufacturing process, so that fracture occurs in the continuous casting process. The chances are high. Also, a large amount of P may be segregated in the grain boundary of the product, thereby reducing the stiffness due to grain boundary fracture.

· S:0.020% 이하 · S: 0.020% or less

S는 Mn과 결합하여 MnS의 석출물을 만든다. MnS는 개재물로 형성되어 균열의 시작점으로 작용할 수 있으므로 적을수록 유리하므로 S의 양을 0.020%이하로 제한하는 것이 바람직하다.S combines with Mn to form a precipitate of MnS. Since MnS is formed as inclusions and can act as a starting point of cracking, it is preferable to limit the amount of S to 0.020% or less since it is more advantageous.

· Al:0.015~0.050% · Al: 0.015 ~ 0.050%

Al은 제강공정에서 첨가되어 강중 O와 반응하여 슬래그를 만들고 용강 상부에서 형성된 슬래그를 제거하여 강중의 O를 없애는 탈산 원소로, 강중의 O를 제거하고 Al이 잔류하게 된다. 본 발명에서는 강 중에 남아 있는 Al을 이용하여 AlN 석출물을 형성시키고 잔류 오스테나이트의 결정립을 감소시켜서 연신율을 향상시키는데 이용한다. 같은 양의 잔류 오스테나이트가 존재할 때 결정립 크기가 작으면서 많은 수의 오스테나이트가 분포할 경우 변형 중에 마르텐사이트로 변태하면서 가공경화속도를 빠르게 하는 효과가 크므로 연신율이 향상되는 것으로 알려져 있다. 잔류 오스테나이트의 크기를 줄이기 위하여는 소둔중에 오스테나이트의 크기를 감소시켜야 한다. 석출물을 형성시키면 결정립 성장을 억제하여 결정립 크기를 줄일 수 있다. 석출물이 과다하게 많은 경우 석출경화에 의하여 강도가 증가하고 연신율이 감소하는 경향이 있으므로 석출물의 양을 줄이면서 오스테나이트의 결정립 크기를 효과적으로 줄이는 것이 중요한다. 철강에서 석출경화의 효과를 얻기 위하여 주로 사용되는 Nb, Ti, V 석출물은 그 크기가 클 뿐 아니라 오스테나이트 안정화 원소인 C결합하여, NbC, TiC, VC 등을 형성하므로 고용 C의 함량을 줄이므로 가공유기변태강에는 적당하지 않다. 이와 같은 것을 종합하면 가공유기변태강에서 연신율을 증가시키기 위하여는 C과 결합하지 않으면서 크기가 작은 석출물을 형성시켜야 된다는 것을 알 수 있다. 본 발명에서는 이러한 역할을 하는 석출물로 AlN를 형성시킨다. AlN은 C의 고용도가 없으며 석출물의 크기가 TiC, NbC, VC 등의 석출물에 비하여 매우 작은 것으로 알려 있다. Al의 양이 0.015%보다 적으면 형성되는 석출물의 수가 적어서 효과적으로 잔류오스테나이트의 크기를 감소시킬 수 없다. 반면 Al의 양이 0.050% 보다 많으면 AlN의 석출물의 조대화 되므로 연신율 형성에 불리하 다. 이러한 이유로 본 발명에서는 Al의 함량을 0.015~0.050%로 제한하는 것이 바람직하다. Al is a deoxidation element that is added in the steelmaking process and reacts with O in the steel to make slag, and removes the slag formed in the upper part of the molten steel to remove O in the steel. The Al in the steel is removed and Al remains. In the present invention, AlN precipitates are formed by using Al remaining in the steel and used to improve elongation by reducing grains of retained austenite. It is known that when the same amount of retained austenite is present, when the grain size is small and a large number of austenite is distributed, the elongation is improved because the effect of transforming to martensite during deformation is great. In order to reduce the size of residual austenite, the size of austenite should be reduced during annealing. Formation of precipitates can suppress grain growth and reduce grain size. When there are too many precipitates, the strength tends to increase due to precipitation hardening and the elongation tends to decrease. Therefore, it is important to effectively reduce the grain size of austenite while reducing the amount of precipitates. Nb, Ti, and V precipitates, which are mainly used to obtain precipitation hardening effect in steel, are not only large in size but also combine with austenite stabilizing elements C to form NbC, TiC, and VC, thus reducing the content of solid solution C. Not suitable for processed organic transformation steel. Taken together, it can be seen that in order to increase the elongation in the processed organic transformation steel, small precipitates should be formed without combining with C. In the present invention, AlN is formed as a precipitate having such a role. AlN has no solid solubility of C and the precipitate is known to have a very small size compared with precipitates such as TiC, NbC, and VC. If the amount of Al is less than 0.015%, the number of precipitates formed is small, so that the size of residual austenite cannot be effectively reduced. On the other hand, if the amount of Al is more than 0.050%, the precipitate of AlN is coarsened, which is disadvantageous in forming elongation. For this reason, in the present invention, it is preferable to limit the content of Al to 0.015 ~ 0.050%.

·N: 0.008~0.026% · N: 0.008 ~ 0.026%

N은 AlN을 형성시키기 위하여 첨가된 성분이다. 일반적인 제철소 제강공정에서 불순물로 첨가되는 N은 0.004%이내이다. 이 발명에서는 AlN 석출물을 형성시켜 결정립 미세화를 이루기 위하여 N을 적극적으로 첨가한다. N은 AlN 형태로 석출되므로 원자량을 고려할 때 다음과 같은 Al (14/27) 로 첨가하는 것이 적당하다. 즉, 0.015~0.050% 의 범위의 Al을 첨가할 때 N의 범위는 0.008 ~ 0.026%로 하는 것이 적당한 것이다. 이러한 범위에서 N을 첨가할 때 적당한 양의 AlN이 형성되어 잔류 오스테나이트의 결정립크기를 감소하여 연신율을 증가시킬 수 있는 것이다. 도2는 AlN 석출물이 오스테나이트 결정립의 이동을 억제하는 것을 보여주는 것으로 소둔 중에 AlN 석출물이 오스테나이트 성장을 억제하는 것을 알 수 있게 하여 준다. N is a component added to form AlN. In general steelworks steelmaking process, N added as an impurity is within 0.004%. In this invention, N is actively added to form AlN precipitates to achieve grain refinement. Since N is precipitated in the form of AlN, it is appropriate to add Al (14/27) as follows in consideration of the atomic weight. That is, when Al in the range of 0.015 to 0.050% is added, it is appropriate that the range of N is 0.008 to 0.026%. When N is added in this range, an appropriate amount of AlN is formed to reduce the grain size of the retained austenite, thereby increasing the elongation. Figure 2 shows that the AlN precipitate inhibits the movement of the austenite grains, and the AlN precipitate inhibits austenite growth during annealing.

· Si과 P의 성분제어 · Control of the components Si and P

도1은 1.5Mn-1.5Si이 첨가된 강과 1.5Mn-1.0Si-0.08P가 첨가된 강의 각각의 상태도를 보여주고 있는 것으로, 1.5Mn-1.5Si이 첨가된 강과 1.5Mn-1.0Si-0.08P가 첨가된 강의 상태도가 같은 것을 알 수 있다. 이것은 상변태 거동에서 0.08% 함량의 P가 0.5% 함량의 Si과 같은 효과가 있다는 것을 보여주고 있다. Si은 용접성을 저하시키는 원소이지만 P는 용접성을 저하시키지 않으므로 Si 함량을 감소시키는 대신 Si 함량의 8/50의 P를 첨가하면 같은 효과의 상변태 변화를 얻음과 동시에 용접성을 향상시킬 수 있는 것이다. 이를 바탕으로 본 발명에서는 Si 과 P의 함량을 다음의 계산식의 범위에서 정한다. Figure 1 shows the state diagrams of the 1.5Mn-1.5Si added steel and 1.5Mn-1.0Si-0.08P added, respectively, 1.5Mn-1.5Si added and 1.5Mn-1.0Si-0.08P It can be seen that the state diagram of the added steel is the same. This shows that in phase transformation behavior, 0.08% P has the same effect as 0.5% Si. Si is an element that lowers the weldability, but P does not lower the weldability. Therefore, by adding P of 8/50 Si content instead of reducing the Si content, the change of phase transformation of the same effect can be obtained and the weldability can be improved. Based on this, in the present invention, the content of Si and P is determined in the range of the following formula.

1.5 ≤ Si[%] + 50/8 P[%] ≤2.01.5 ≤ Si [%] + 50/8 P [%] ≤2.0

[강 제조조건]Steel manufacturing conditions

상기와 같이 조성되는 강을 열간압연하여 권취한 다음, 열간압연판을 냉간압연한 후에 연속소둔하고, 열처리하여 냉간압연판으로 제공된다. 본 발명에서는 이러한 제조조건에서 냉간압연판의 연속소둔공정과 오스템퍼링조건을 제어하는데, 특징이 있다. 따라서, 열간압연조건과 냉간압연조건은 여러 가지 다양한 기술을 통해 제조할 수 있으며, 그 대표적인 기술을 예로 들어 열간압연공정과 냉간압연공정에서 그 제조조건을 구체적인 예로 들어 설명하지만 본 발명이 여기에 제한되는 것이 아니다. The steel formed as described above is hot rolled and wound. Then, the hot rolled plate is cold rolled and then continuously annealed and heat treated to provide a cold rolled plate. In the present invention, there is a feature in controlling the continuous annealing process and the tempering conditions of the cold rolled sheet under such manufacturing conditions. Therefore, the hot rolling conditions and the cold rolling conditions can be manufactured through a variety of techniques, the representative technology described in the hot rolling process and cold rolling process as a specific example, but the present invention is limited thereto. It is not.

·열간압연공정 · Hot rolling

상기와 같이 조성되는 강을 고온에서 재가열하여 열간압연한다. 재가열온도는 1050~1300℃가 바람직하다. 상기와 같이 재가열하여 열간압연하는데, 이때의 마무리압연온도는 890~940℃로 하는 것이 바람직하다. 상기와 같이 압연하여 권취하는데, 이때의 권취온도는 600~700℃로 하는 것이 바람직하다. The steel formed as described above is reheated at high temperature and hot rolled. The reheating temperature is preferably 1050 to 1300 ° C. Reheating and hot rolling as described above, the finish rolling temperature at this time is preferably 890 ~ 940 ℃. Although rolling by winding as above, it is preferable that the coiling temperature at this time shall be 600-700 degreeC.

·냉간압연공정 - cold rolling

상기에서 얻은 열간압연판을 산세하여 냉간압연하는데, 이때의 냉간압하율은 40~70%로 하는 것이 바람직하다. The hot rolled plate obtained above is pickled and cold rolled, and the cold reduction rate at this time is preferably 40 to 70%.

·연속소둔공정 · Continuous Annealing Process

본 발명과 같이 C, Si, Mn을 함유한 강을 이용하여 연신율을 증가시키기 위하여는 잔류 오스테나이트의 함량을 증가시켜야 한다. 본 발명의 연구에 따르면 잔류 오스테나이트를 증가시키기 위하여는 열처리 사이클을 성분에 적합하게 설정하여야 한다는 것이다. In order to increase the elongation using the steel containing C, Si, Mn as in the present invention, the content of residual austenite must be increased. According to the study of the present invention, in order to increase the residual austenite, the heat treatment cycle should be set appropriately for the components.

연속소둔로를 이용하여 소둔할 때 잔류 오스테나이트를 만들기 위하여는 어닐링하여 오스테나이트를 만들고 오스템퍼링 온도까지 냉각하여 오스템퍼링하여 베이나이트를 형성하면서 고용 C을 잔류 오스테나이트로 확산시켜서 오스테나이트를 안정화시켜야 한다. 이 때 소둔온도를 잘 설정하는 것이 중요하다. 소둔온도가 너무 낮으면 열연강판에 존재하는 퍼얼라이트가 용해되지 못하여 오스테나이트의 안정성을 저하시킨다. 또한 소둔온도가 너무 높으면 오스테나이트가 너무 많이 형성되고 페라이트가 적어지므로 최종적으로 베이나이트가 만이 형성되어 강도가 증가하고 연신율이 감소한다. 이러한 것을 고려하여 각 성분의 강에 대한 최적의 소둔온도를 설정하는 것이 중요하다. In order to make residual austenite when annealed using a continuous annealing furnace, an austenite must be annealed to form austenite, cooled to an ostempering temperature, and austened to form bainite, while dissolving solid solution C into residual austenite to stabilize austenite. do. At this time, it is important to set the annealing temperature well. If the annealing temperature is too low, the pearlite present in the hot-rolled steel sheet cannot be dissolved, thereby reducing the stability of austenite. In addition, if the annealing temperature is too high, too much austenite is formed and the ferrite becomes less, so only bainite is finally formed, thereby increasing strength and decreasing elongation. In view of this, it is important to set the optimum annealing temperature for the steel of each component.

소둔온도 결정에 크게 영향을 주는 원소는 C, Si, Mn이므로 본 발명에서는 이들 성분을 변화시켜 제조한 강을 각 소둔온도에서 51sec 동안 유지하였을 때 오스테나이트의 양을 측정하는 실험을 통해 연속소둔온도를 설정한 것이다. 그 실험결과를 나타낸 것이 도 3이다. 도 3의 성분계를 갖는 강을 이용하여 잔류 오스테나이트의 양을 증가시키기 위하여는 최대의 페라이트를 형성시켜서 오스테나이트에 최대의 고용 C을 확산시켜야 하는 것이다. 페라이트의 분율을 최대로 증가시키면서 퍼얼라이트는 반드시 용해되어야 한다. 퍼얼라이트에는 탄화물이 다량 존재하므로 퍼얼라이트가 존재하면 오스테나이트로 확산되어 가는 고용 C이 줄어들기 때문이다. 퍼얼라이트를 완전히 용해시키기 위하여 C의 함량이 0.1, 0.15, 0.20%인 각각의 강에서 오스테나이트의 양이 19, 28, 38%가 되어야 한다. 이 이상의 오스테나이트를 형성하게 되면 페라이트의 양이 줄어들기 때문에 잔류 오스테나이트를 많이 형성시키기 어렵다. 이러한 조건하에서 퍼얼라이트를 완전히 용해시키는 소둔온도는 563 + 651 C[%] + 42 Si[%] + 18 Mn[%] 이고 소둔온도가 850℃ 이상에서는 오스테나이트가 너무 많이 형성되므로 이 온도 이하에서 소둔하는 것이 적당하다. 따라서 가장 적당한 소둔온도 범위는 다음과 같다. The elements that greatly influence the determination of annealing temperature are C, Si, and Mn, so in the present invention, the continuous annealing temperature is measured by measuring the amount of austenite when the steel produced by changing these components is maintained at each annealing temperature for 51 sec. Is set. 3 shows the results of the experiment. In order to increase the amount of retained austenite using the steel having the component system of FIG. 3, it is necessary to form the maximum ferrite to diffuse the maximum solid solution C in the austenite. Perlite must be dissolved while maximizing the fraction of ferrite. Since there is a large amount of carbides in Perlite, the presence of Perlite reduces the amount of solid solution C spread to austenite. In order to completely dissolve the pearlite, the amount of austenite in each steel with a C content of 0.1, 0.15 and 0.20% must be 19, 28 and 38%. If the austenite is formed more than this, the amount of ferrite is reduced, so it is difficult to form a large amount of retained austenite. Under these conditions, the annealing temperature to completely dissolve the pearlite is 563 + 651 C [%] + 42 Si [%] + 18 Mn [%], and the annealing temperature is higher than 850 ° C, so much austenite is formed. It is suitable to anneal. Therefore, the most suitable annealing temperature range is as follows.

563 + 651 C[%] + 42 Si[%] + 18 Mn[%] < 소둔온도 [℃] ≤ 850℃563 + 651 C [%] + 42 Si [%] + 18 Mn [%] <Annealing Temperature [℃] ≤ 850 ℃

본 발명에서는 상기한 연속소둔온도범위에서 50sec 이상 소둔하여 적정한 오스테나이트를 확보하는 것이다. In the present invention, by annealing for 50 seconds or more in the continuous annealing temperature range described above to ensure the proper austenite.

·오스템퍼링 열처리 Agarose, tempering heat treatment

소둔 구간에서 오스테나이트가 형성된 재료를 퍼얼라이트라 형성되지 않도록 오스템퍼링 개시온도 400~450℃ 까지 급냉한 후 350~450℃까지 200~500sec 동안에 냉각하는 오스템퍼링을 실시한다. 연속소둔구간에서 오스템페링개시온도까지는 급냉하는데, 이때의 냉각속도는 약 20~100℃/sec 로 하는 것이 바람직하다. 오스템퍼링할 때 소둔구간 형성된 오스테나이트의 일부가 베이나이트로 형성되고 고용 C이 잔류 오스테나이트로 확산되어 잔류 오스테나이트가 안정화된다. In the annealing section, the austenite-formed material is quenched to austelling start temperature of 400 ~ 450 ℃ to prevent the formation of a pearlite, and then osstem cooling to 200 ~ 500 sec to 350 ~ 450 ℃. Rapid cooling from the continuous annealing section to the starting temperature of ossempering, the cooling rate is preferably about 20 ~ 100 ℃ / sec. When austempering, a portion of the austenite formed in the annealing section is formed as bainite, and the solid solution C diffuses into the residual austenite to stabilize the residual austenite.

본 발명에서 소둔구간에서 오스템퍼링개시온도인 400~450℃까지 급냉하는 것이 바람직하다. 그리고, 오스템퍼링개시온도에서 350~450℃까지 200~500sec동안에 냉각한다. In the present invention, it is preferable to quench to 400 ~ 450 ℃ the start tempering temperature in the annealing section. Then, it is cooled for 200 to 500 sec from the tempering start temperature to 350 to 450 ° C.

이하 본 발명을 실시예를 통하여 보다 구체적으로 설명한다. Hereinafter, the present invention will be described in more detail with reference to Examples.

[실시예 1]Example 1

표1 성분의 각 강을 용해하고 열간압연을 실시하였다. 연간압연시 재가열온도는 1250℃, 마무리온도는 910℃, 권취온도는 600℃로 작업하였다. 열간압연판의 표면 산화층을 산세로 제거한 후 50% 냉간압연을 실시하여 1.4mm 두께의 내연강판을 제조하였다. 냉간압연한 강판을 연속소둔로에서 열처리하였으며 열처리시 소둔시간은 51~102sec로 하였고 오스템퍼링 시간은 300초로 하였다. 열처리조건별 냉연강판의 재질 측정 결과를 표 2에 나타내었다. Each steel of Table 1 component was melted and hot-rolled. During the annual rolling, the reheating temperature was 1250 ℃, the finishing temperature was 910 ℃, and the winding temperature was 600 ℃. After removing the surface oxide layer of the hot rolled plate by pickling, 50% cold rolling was performed to prepare a 1.4 mm thick internal rolled steel sheet. The cold rolled steel sheet was heat-treated in a continuous annealing furnace, and the annealing time was 51 to 102 sec and the tempering time was 300 sec. Table 2 shows the measurement results of the material of the cold rolled steel sheets according to the heat treatment conditions.

River CC MnMn SiSi PP SS S-AlS-Al NN Si+50/8PSi + 50 / 8P 소둔온도 하한Annealing temperature lower limit 비고Remarks A1A1 0.200.20 1.511.51 1.051.05 0.0720.072 0.0100.010 0.0350.035 0.01000.0100 1.51.5 784784 발명강Invention steel A2A2 0.190.19 1.581.58 1.201.20 0.1000.100 0.0050.005 0.0490.049 0.01400.0140 1.81.8 766766 A3A3 0.200.20 1.481.48 0.900.90 0.0800.080 0.0030.003 0.0340.034 0.01200.0120 1.41.4 758758 A4A4 0.200.20 1.461.46 0.700.70 0.1000.100 0.0030.003 0.0340.034 0.01100.0110 1.31.3 749749 B1B1 0.100.10 2.352.35 1.441.44 0.0110.011 0.0090.009 0.0350.035 0.00200.0020 1.51.5 731731 비교강Comparative steel B2B2 0.140.14 1.791.79 1.431.43 0.0130.013 0.0110.011 0.0390.039 0.00360.0036 1.51.5 746746 B3B3 0.200.20 1.331.33 1.701.70 0.0110.011 0.0090.009 0.0370.037 0.00200.0020 1.761.76 789789 소둔온도하한은 563 + 651 C[%] + 42 Si[%] + 18 Mn[%] 의 식으로 계산된 값임 The annealing temperature lower limit is calculated using the formula 563 + 651 C [%] + 42 Si [%] + 18 Mn [%].                                             

River 소둔 온도 (℃)Annealing Temperature (℃) 소둔시간 (SEC)Annealing Time (SEC) 오스템 퍼링 개시온도 (℃)Osstem Furring Start Temperature (℃) 오스템 퍼링 시간 (SEC)Ostem Furring Time (SEC) 항복강도 (kgf/mm2)Yield strength (kgf / mm 2 ) 인장강도 (kgf/mm2)Tensile Strength (kgf / mm 2 ) 연신율 (%)Elongation (%) 플래시버트 용접성Flash Butt Weldability 비고Remarks A1A1 800800 5151 400400 300300 44.3744.37 74.2374.23 34.0234.02 발명강Invention steel A1A1 830830 5151 400400 300300 40.7140.71 80.5380.53 31.1731.17 A1A1 800800 5151 450450 300300 42.9942.99 81.0181.01 30.1430.14 A1A1 830830 5151 450450 300300 43.7443.74 81.1381.13 29.3829.38 A1A1 800800 102102 400400 300300 42.9042.90 80.6080.60 29.1029.10 A2A2 800800 5151 400400 300300 44.9844.98 74.1674.16 30.5330.53 A2A2 830830 5151 400400 300300 43.2343.23 75.1375.13 31.3431.34 A2A2 830830 5151 450450 300300 45.1045.10 72.4472.44 28.9328.93 A2A2 800800 102102 400400 300300 45.9045.90 76.9076.90 29.3029.30 A3A3 830830 5151 400400 300300 43.9143.91 80.2680.26 29.3529.35 A4A4 830830 5151 400400 300300 42.0642.06 81.9081.90 30.3130.31 B1B1 800800 5151 400400 300300 41.1041.10 83.8083.80 21.6021.60 비교강Comparative steel B1B1 800800 5151 450450 300300 40.3040.30 92.1092.10 17.4017.40 B1B1 800800 5151 500500 300300 41.5041.50 85.3085.30 16.2016.20 B1B1 800800 102102 450450 300300 40.3040.30 92.1092.10 17.4017.40 B2B2 800800 5151 400400 300300 42.6042.60 76.1076.10 23.1023.10 B2B2 800800 5151 450450 300300 36.5036.50 82.5082.50 23.8023.80 B2B2 800800 5151 500500 300300 47.0047.00 68.5068.50 23.2023.20 B2B2 800800 102102 450450 300300 36.5036.50 82.5082.50 23.8023.80 B3B3 800800 5151 450450 300300 47.8047.80 71.0071.00 20.8020.80 ×× B3B3 800800 5151 500500 300300 55.6055.60 70.8070.80 23.2023.20 ×× B3B3 800800 102102 450450 300300 47.8047.80 71.0071.00 20.8020.80 ××

표 1, 2에 나타난 바와 같이, 본 발명을 만족하는 강은 비교재에 비하여 항복강도가 높은 것을 알 수 있다. As shown in Tables 1 and 2, it can be seen that the steel satisfying the present invention has a higher yield strength than the comparative material.

상술한 바와 같이, 본 발명은 연신율이 높아서 성형성이 우수한 고강도 강판을 제공할 수 있으며, 이 고강도 강판은 자동차 구조용 부품에 사용하여 자동차의 안정성을 향상시킬 수 있는 유용한 효과가 있는 것이다.
As described above, the present invention can provide a high-strength steel sheet having high elongation and excellent moldability, and this high-strength steel sheet has a useful effect of improving the stability of an automobile by using it for automotive structural parts.

Claims (3)

중량%로, C: 0.15~0.25 %, In weight%, C: 0.15-0.25%, Si: 0.5~1.2%,Si: 0.5-1.2%, Mn: 1.0~2.0%, Mn: 1.0-2.0%, P: 0.25%이하,P: 0.25% or less, S: 0.020%이하,S: 0.020% or less, Al: 0.015 ~ 0.050%, Al: 0.015-0.050%, N: 0.008 ~0.026%,N: 0.008-0.026%, 상기 Si와 P가 다음의 관계를 만족하고, 1.5 ≤ Si[%] + 50/8 P[%] ≤2.0Si and P satisfy the following relationship, and 1.5 ≦ Si [%] + 50/8 P [%] ≦ 2.0 나머지 Fe와 불가피한 불순물로 조성되는 성형성 및 용접성이 우수한 고강도 냉연강판. High strength cold rolled steel sheet with excellent formability and weldability composed of remaining Fe and unavoidable impurities. 중량%로, C: 0.15~0.25 %, Si: 0.5~1.2%, Mn: 1.0~2.0 %, P: 0.25 % 이하, S: 0.020%이하By weight%, C: 0.15-0.25%, Si: 0.5-1.2%, Mn: 1.0-2.0%, P: 0.25% or less, S: 0.020% or less Al: 0.015 ~ 0.050%, N: 0.008 ~0.026%, 상기 Si와 P가 다음의 관계, 1.5 ≤ Si[%] + 50/8 P[%] ≤2.0를 만족하고 나머지 Fe와 불가피한 불순물로 조성되는 냉간압연판을 아래 관계식 2의 범위의 온도에서 50sec이상 연속소둔하는 단계, Al: 0.015 to 0.050%, N: 0.008 to 0.026%, wherein Si and P satisfy the following relationship, 1.5 ≦ Si [%] + 50/8 P [%] ≦ 2.0 and are composed of the remaining Fe and unavoidable impurities Continuously annealing the cold rolled sheet at a temperature in the range of the following relation 2 for at least 50 sec, [관계식 2][Relationship 2] 563 + 651 C[%] + 42 Si[%] + 18 Mn[%] < 소둔온도 [℃] ≤ 850℃563 + 651 C [%] + 42 Si [%] + 18 Mn [%] <Annealing Temperature [℃] ≤ 850 ℃ 상기 연속소둔하고 20~100℃/sec 냉각속도로 오스템퍼링 개시온도 400~450℃ 까지 급랭한 후 350~400℃까지 200~500sec 동안에 냉각하는 오스템퍼링하는 단계를 포함하여 이루어지는 성형성 및 용접성이 우수한 고강도 냉연강판의 제조방법. Excellent continuous formability and weldability comprising the step of continuous annealing and quenching the ostempering start temperature 400 ~ 450 ℃ at a cooling rate of 20 ~ 100 ℃ / sec and then cooling to 200 ~ 500 sec to 350 ~ 400 ℃ Method for producing high strength cold rolled steel sheet. 제 2항에 있어서, 상기 냉간압연판은 강을 1050~1300℃의 온도로 재가열하여 890~940℃의 마무리압연온도조건으로 열간압연하여 열간압연판을600~700℃의 온도에서 권취한 다음, 산세하고 40~70%의 냉간압하율로 냉간압연하여 얻은 것을 특징으로 하는 성형성 및 용접성이 우수한 고강도 냉연강판의 제조방법. The method of claim 2, wherein the cold rolled steel is reheated to a temperature of 1050 ~ 1300 ℃ hot rolled to a finish rolling temperature conditions of 890 ~ 940 ℃ wound the hot rolled plate at a temperature of 600 ~ 700 ℃, A method for producing a high strength cold rolled steel sheet having excellent formability and weldability, which is obtained by pickling and cold rolling at a cold reduction ratio of 40 to 70%.
KR1020010085539A 2001-12-27 2001-12-27 High strength cold rolled steel sheet with superior formability and weldability and method for manufacturing thereof KR100554753B1 (en)

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JP2003556557A JP3895728B2 (en) 2001-12-27 2002-06-20 High-strength cold-rolled steel sheet excellent in formability and weldability and its manufacturing method
EP02741471A EP1458896A4 (en) 2001-12-27 2002-06-20 High strength cold rolled steel sheet with superior formability and weldability, and manufacturing method therefor
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JP2005513271A (en) 2005-05-12
US20040238083A1 (en) 2004-12-02
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WO2003056041A1 (en) 2003-07-10
EP1458896A1 (en) 2004-09-22
EP1458896A4 (en) 2004-12-29

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