WO2016093513A2 - 성형성이 우수한 복합조직강판 및 이의 제조방법 - Google Patents
성형성이 우수한 복합조직강판 및 이의 제조방법 Download PDFInfo
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- C21D2211/00—Microstructure comprising significant phases
- C21D2211/008—Martensite
Definitions
- the present invention relates to a high-strength steel sheet, and more particularly, to a composite structured steel sheet and a method for manufacturing the same, which are excellent in formability and suitable for use in automobile panels.
- high-strength steels are being actively used to satisfy both lightweight and high-strength automobile bodies, and the application of high-strength steels to automobile exteriors is expanding.
- the steel sheet applied to the exterior of the automobile should be excellent surface quality above all, it is difficult to secure the surface quality of the coating due to the hardenable elements and oxidizing elements (for example, Si, Mn, etc.) added to ensure high strength to be.
- the hardenable elements and oxidizing elements for example, Si, Mn, etc.
- alloyed hot-dip galvanized steel sheet which is heat-treated again after hot-dip galvanizing is widely used in view of excellent corrosion resistance and weldability and formability.
- Patent Document 1 discloses a steel sheet having a composite structure mainly composed of martensite as a conventional technique for improving workability in high tensile steel sheets, and a high tensile strength steel sheet in which fine Cu precipitates having a particle size of 1 to 100 nm are dispersed in a structure to improve workability.
- a manufacturing method is disclosed.
- Patent Document 1 it is necessary to add an excess of 2 to 5% of Cu in order to precipitate fine Cu particles, which may cause red brittleness resulting from Cu and excessively increase manufacturing costs.
- Patent Document 2 discloses a composite steel sheet comprising ferrite as a main phase, residual austenite as a two phase, and bainite and martensite as a low temperature transformation phase, and a method for improving the ductility and extension flange of the steel sheet.
- Patent Document 2 has a problem in that it is difficult to secure the plating quality by adding a large amount of Si and Al to secure the retained austenite phase, it is difficult to secure the surface quality during steelmaking and performance.
- due to the metamorphic organic plasticity has a high yield ratio high initial YS value.
- Patent Document 3 is a technique for providing a high-strength hot-dip galvanized steel sheet having good workability, and a steel sheet comprising a composite of soft ferrite and hard martensite as a microstructure, and to improve its elongation and r value (Lankford value). A manufacturing method is disclosed.
- this technique not only ensures excellent plating quality as a large amount of Si is added, but also causes a problem in that the manufacturing cost increases due to the addition of a large amount of Ti and Mo.
- Patent Document 1 Japanese Unexamined Patent Publication No. 2005-264176
- Patent Document 2 Japanese Unexamined Patent Publication No. 2004-292891
- Patent Document 3 Korean Unexamined Patent Publication No. 2002-0073564
- One aspect of the present invention relates to a composite structure steel sheet suitable as a steel sheet for automotive exterior plate, composite structure steel sheet having excellent moldability that can significantly improve the ductility (EL / YR) compared to yield ratio by optimizing alloy design and manufacturing conditions And to provide a method for producing the same.
- the steel sheet includes ferrite as a main phase, has a fine martensite fraction of 1 to 8% at a point of 1 / 4t based on the total thickness (t), and has an average particle diameter of 1 ⁇ m existing in a ferrite grain boundary defined by the following formula (1).
- the occupancy ratio (M%) of less than martensite is 90% or more, and the moldability is that the area ratio (B%) of bainite is 3% or less (including 0%) in the total two-phase structure defined by the following formula (2): Provides excellent composite steel sheet.
- M (%) ⁇ M gb / (M gb + M in ) ⁇ ⁇ 100
- the step of reheating the steel slab satisfying the above-described component system Manufacturing a hot rolled steel sheet by finishing hot rolling of the reheated steel slab at an Ar3 transformation point or more; Winding the hot rolled steel sheet at 450 to 700 ° C; Manufacturing the cold rolled steel sheet by cold rolling the wound hot rolled steel sheet at a reduction ratio of 40 to 80%; And annealing the cold rolled steel sheet at a temperature range of 760 to 850 ° C. in a continuous annealing furnace or an alloyed hot dip plating furnace.
- the annealed steel sheet includes ferrite as a main phase, and has a fine martensite fraction of 1 to 8% at a point of 1 / 4t based on the total thickness (t) and an average present in the ferrite grain boundary defined by Equation (1).
- the occupancy ratio (M%) of martensite having a particle diameter of less than 1 ⁇ m is 90% or more, and the area ratio (B%) of bainite is 3% or less (including 0%) in the total two-phase structure defined by the formula (2).
- a method for producing a composite tissue steel sheet having excellent moldability is provided.
- According to the present invention can provide a composite tissue steel sheet that can ensure excellent strength and ductility at the same time excellent, it has an effect that is suitable for automotive exterior plates that require high processability.
- FIG. 1 is a graph showing the change in yield ratio (YS / TS) according to the temper reduction rate of the composite tissue steel sheet according to an aspect of the present invention.
- the present inventors have studied in depth to provide a steel sheet excellent in formability by securing strength and ductility at the same time to be suitable for automotive exterior panels, provide a composite structured steel sheet that satisfies the intended properties by optimizing the manufacturing conditions with alloy design It confirmed that it was possible and came to complete this invention.
- Composite tissue sheet according to the present invention by weight%, carbon (C): 0.01 ⁇ 0.08%, manganese (Mn): 1.5 ⁇ 2.5%, chromium (Cr): 1.0% or less (excluding 0%), silicon (Si ): 1.0% or less (except 0%) Phosphorus (P): 0.1% or less (except 0%), sulfur (S): 0.01% or less (excluding 0%), nitrogen (N): 0.01% or less ( 0% excluding), acid value aluminum (sol.Al): 0.02 ⁇ 0.1%, molybdenum (Mo): 0.1% or less (excluding 0%), boron (B): 0.003% or less (excluding 0%), It is preferable that the balance consists of Fe and other unavoidable impurities, and the sum of the weight percentages of Mn and Cr (Mn + Cr) satisfies 1.5 to 3.5%.
- the content of each component means all by weight.
- Carbon (C) is an important component for producing a steel sheet having a composite structure, which is an advantageous element for forming strength martensite, one of the two-phase structure.
- C Carbon
- YS / TS intended strength and yield ratio
- the bainite transformation occurs at the time of annealing and cooling, thereby increasing the yield ratio of the steel.
- the content of C it is preferable to control the content of C to 0.01% or more. If the content of C is less than 0.01%, it is difficult to secure the strength of the 490MPa grade targeted in the present invention, and it is difficult to form an appropriate level of martensite. On the other hand, if the content exceeds 0.08%, the grain boundary bainite formation is promoted upon cooling after annealing, so that the yield strength is increased, so that bending and surface defects occur easily when processing automotive parts. Therefore, in the present invention, it is preferable to control the content of C to 0.01 ⁇ 0.08%.
- Manganese (Mn) is an element that improves hardenability in a steel sheet having a composite structure, and is particularly important in forming martensite.
- Existing solid solution strengthening steel is effective to increase strength due to solid solution strengthening effect, and precipitates S, which is inevitably added in steel, to MnS, and plays an important role in suppressing plate breakage caused by S and high temperature embrittlement during hot rolling.
- Mn manganese-doped-silicon
- Chromium (Cr) is a component having properties similar to those of Mn described above, and is an element added to improve the hardenability of steel and to secure high strength. Such Cr is effective in forming martensite, and forms coarse Cr-based carbides such as Cr 23 C 6 in the hot rolling process, thereby suppressing the yield point yield (YP-El) by precipitating the amount of solid solution C in the steel below an appropriate level. It is an advantageous element for the production of composite steel with low yield ratio. In addition, it is advantageous to manufacture a composite tissue steel having a high ductility by minimizing the decrease in elongation compared to the increase in strength.
- the Cr facilitates the formation of martensite through improving the hardenability, but if the content exceeds 1.0%, there is a problem of excessively increasing the martensite formation rate, resulting in a decrease in strength and elongation. Therefore, in the present invention, it is preferable to limit the content of Cr to 1.0% or less, and 0% is excluded in consideration of the amount inevitably added in production.
- Mn and Cr are important elements for improving the hardenability, and when the composite tissue steel is prepared by adding C in excess of 0.08% to form martensite, the production of the composite tissue steel is low even though the content of Mn and Cr is low. Possible, but in this case, there is a problem that the elongation is lowered and it is difficult to manufacture a resistive steel sheet.
- the content of C is added as low as possible, and instead, the content of Mn and Cr, which are strong hardenability elements, is controlled to form an appropriate level of martensite, thereby achieving physical properties such as improvement in resistance ratio and elongation. can do.
- the yield ratio that is, the yield strength is rapidly increased compared to the tensile strength, there is a problem that defects such as crack generation and bending occurs easily when processing the part. Therefore, in the present invention, it is preferable to control the sum of the contents of Mn and Cr to 1.5 to 3.5%.
- silicon is an element which contributes to the improvement of elongation by forming residual austenite at an appropriate level during annealing, but exhibits its characteristics when the C content is high as about 0.6%.
- the Si serves to improve the strength of the steel through a solid solution strengthening effect, or is known to improve the surface properties of the plated steel sheet at an appropriate level or more.
- the content of Si is limited to 1.0% or less (excluding 0%), in order to secure strength and improve elongation.
- 0% is excluded in consideration of the amount inevitably added in manufacturing. If the content of Si exceeds 1.0%, the plating surface properties are inferior, and the amount of solid solution C is low, so that residual austenite is not formed.
- Phosphorus (P) in steel is the most favorable element to secure the strength without increasing the formability, but excessive addition greatly increases the possibility of brittle fracture, which increases the possibility of plate breakage of the slab during hot rolling. There is a problem of acting as an element that inhibits properties.
- the content of P is limited to a maximum of 0.1%, except for 0% in consideration of the inevitably added level.
- S Sulfur
- S in steel has a problem of increasing the possibility of generating red brittleness, it is preferable to control the content to 0.01% or less.
- 0% is excluded in consideration of the level inevitably added during the manufacturing process.
- N Nitrogen
- Acid soluble aluminum (sol.Al) is an element added to refine the particle size and deoxidation of the steel. If the content is less than 0.02%, aluminum killed steel cannot be manufactured in a stable state. When it exceeds 0.1%, the grain refinement effect is advantageous to increase the strength, while the excessive formation of inclusions during steelmaking operation increases the possibility of surface defects on the plated steel sheet, and increases the manufacturing cost. Therefore, in the present invention, it is preferable to control the content of sol.Al to 0.02 to 0.1%.
- Molybdenum is an element added to delay the transformation of austenite into pearlite and to refine the ferrite and improve the strength.
- Mo has the advantage that the yield ratio can be controlled by finely forming martensite at a grain boundary by improving the hardenability of the steel.
- disadvantages in manufacturing as the content of the expensive element increases, it is preferable to control the content appropriately.
- the optimal level of Mo in the present invention is 0.05%, it is not unreasonable to secure the desired physical properties even if not necessarily added. However, 0% is excluded in consideration of the level inevitably added during the manufacturing process.
- Boron (B) in steel is an element added in order to prevent secondary work embrittlement by P addition.
- the content of B exceeds 0.003%, there is a problem that the elongation is lowered, so the content of B is controlled to 0.003% or less, in which case 0% is excluded in consideration of the inevitably added level.
- this invention consists of remainder Fe and other unavoidable impurities other than the said component.
- the composite tissue steel sheet of the present invention that satisfies the above-described component composition preferably includes martensite (M) in columnar ferrite (F) and biphasic phase as its microstructure, and may include some bainite (B).
- the martensite is preferably contained 1 to 8% by area fraction of the entire microstructure.
- the fraction of fine martensite satisfies 1 to 8% at a 1 / 4t point based on the total thickness t. If the fraction is less than 1%, it is difficult to secure the strength, whereas if the fraction exceeds 8%, the strength is too high to secure the desired workability.
- the occupancy ratio (M%) of the martensite less than 1 micrometer of average particle diameters which exist in a ferrite grain boundary defined by following formula (1) satisfy
- M (%) ⁇ M gb / (M gb + M in ) ⁇ ⁇ 100
- M gb number of martensites present in the ferrite grain boundary and M in : number of martensite present in the ferrite grain grain.
- the martensite has an average particle diameter of 1 ⁇ m or less.
- the yield ratio before the temper rolling can be controlled to 0.55 or less, and then the tempering rolling can be controlled to the yield ratio of an appropriate level.
- the occupancy ratio of the martensite is less than 90%, the martensite formed in the crystal grains increases the yield strength during tensile deformation, resulting in a high yield ratio, which makes it impossible to control the yield ratio through temper rolling.
- the elongation is lowered, because martensite present in the crystal grains significantly prevents the progress of dislocations during processing, so that the yield strength proceeds faster than the tensile strength, and also a large amount of martensite is formed in the ferrite grain. This is because excessively large potentials are generated to hinder the movement of movable potentials during processing.
- the composite tissue steel sheet of the present invention preferably satisfies 3% or less of the area ratio (B%) of bainite in the total two-phase structure defined by the following formula (2).
- the present invention it is important to control the bainite area ratio of the total two-phase structure low, which means that the solid solution elements C and N, which are bainite in the bainite grains, are easily fixed to the potentials to prevent dislocations and discontinuities. This is because the yield ratio is significantly increased by showing the yield behavior.
- the yield ratio before the temper rolling can be managed to 0.55 or less, and then the tempering rolling can be controlled to the yield level of an appropriate level. If the bainite area ratio exceeds 3%, the yield ratio before temper rolling exceeds 0.55, making it difficult to manufacture a resistive-complex composite tissue sheet, which causes a ductility drop.
- Composite tissue sheet of the present invention that satisfies both the composition and the microstructure described above is capable of controlling the yield ratio through the temper rolling, it can be achieved by controlling the temper reduction rate.
- the value (calculated value) derived from the conditional expression defined by Equation (3) can be defined as the yield ratio theoretically derived, through which the intended resistance ratio ratio or high yield ratio type composite steel sheet can be provided. have.
- the temper reduction ratio can be applied as 0.86 ⁇ 2.0%.
- the composite tissue steel sheet of the present invention is capable of manufacturing a steel sheet having a desired yield ratio by controlling the temper reduction rate.
- the composite tissue steel sheet of the present invention is reheated to a steel slab that satisfies the above-described component system under normal conditions, and then hot rolled to produce a hot rolled steel sheet and then wound. Thereafter, the wound hot rolled steel sheet is cold rolled at an appropriate rolling rate to be manufactured as a cold rolled steel sheet, and then manufactured by annealing in a continuous annealing furnace or an alloyed hot dip continuous furnace.
- the present invention it is preferable to reheat the steel slab formed as described above under normal conditions, in order to smoothly perform the subsequent hot rolling process and to sufficiently obtain the properties of the target steel sheet.
- the present invention is not particularly limited to such reheating conditions, and may be normal conditions.
- the reheating process may be performed at a temperature range of 1100 to 1300 ° C.
- the hot-rolled steel sheet by hot-rolling the reheated steel slab under Ar3 transformation point or more under normal conditions.
- the present invention is not limited to the above conditions for finishing hot rolling and can use a normal hot rolling temperature.
- the finish hot rolling may be performed at a temperature range of 800 to 1000 ° C.
- the hot-rolled steel sheet manufactured according to the above it is preferable to wind up the hot-rolled steel sheet manufactured according to the above at 450-700 degreeC.
- the coiling temperature is less than 450 °C excessive martensite or bainite is generated to cause excessive strength increase of the hot-rolled steel sheet, there is a fear that problems such as shape defects due to the subsequent cold rolling load may occur.
- the coiling temperature exceeds 700 °C, there is a problem that the surface thickening by elements that reduce the wettability of molten zinc plating, such as Si, Mn, B in the steel. Therefore, in consideration of this, it is preferable to control the winding temperature to 450 ⁇ 700 °C.
- the wound hot rolled steel sheet is preferably pickled and cold rolled into a cold rolled steel sheet.
- the cold rolling is preferably carried out at a reduction ratio of 40 to 80%, if the cold reduction ratio is less than 40%, there is a problem that it is difficult to secure the target thickness and the shape correction of the steel sheet is difficult, while exceeding 80% If the crack is likely to occur in the steel sheet edge (edge), there is a problem that brings the load of cold rolling.
- the continuous annealing process is for forming ferrite and austenite and distributing carbon at the same time as recrystallization. If the temperature is less than 760 ° C, not only sufficient recrystallization is performed, but also it is difficult to form sufficient austenite in the present invention. There is a problem that it is difficult to secure the intended strength. On the other hand, if it exceeds 850 °C productivity decreases, austenite is excessively generated, there is a problem that bainite is included after cooling to reduce the ductility. Therefore, in consideration of this, it is preferable to control the continuous annealing temperature range to 760 ⁇ 850 °C.
- the steel sheet manufactured according to the above is a composite tissue steel sheet intended in the present invention, and preferably, its internal structure includes ferrite and martensite in a main phase.
- the fraction of martensite having a fine martensite fraction of 1 to 8% at a point of 1 / 4t based on the total thickness (t) and an average particle diameter of less than 1 ⁇ m existing in the ferrite grain boundary defined by the formula (1) (M) %) Is 90% or more
- the area ratio (B%) of bainite among all the two-phase structures defined by the formula (2) satisfies 3% or less.
- the description of the internal structure and the numerical limitation thereof is as mentioned above.
- the present invention it is preferable to perform the temper rolling process after the continuous annealing, it is possible to adjust the yield ratio of the steel sheet through the temper rolling process. More specifically, the present invention can provide an intended composite tissue sheet of resistive ratio or high yield ratio from controlling the temper reduction ratio.
- the yield potential is lowered by lowering the yield strength compared to the tensile strength by facilitating material deformation during tensile deformation.
- Steel sheet which satisfies the range of 0.45-0.6 can be manufactured.
- temper rolling is not carried out, a minimum yield ratio can be secured, but temper rolling at a minimum temper rolling rate is preferable for adjusting the shape of the steel sheet and uniformizing the plating layer. Therefore, 0% is excluded.
- the temper reduction ratio In order to manufacture such a high yield ratio composite tissue steel sheet, it is preferable to control the temper reduction ratio to 0.86% or more. If the temper reduction ratio exceeds 2.0%, the yield ratio exceeds 0.8 and thus the composite tissue steel Loss of function and excessively high yield strength results in a problem that spring back occurs during machining of the part.
- the composite tissue steel sheet of the present invention is a steel sheet which can control yield ratio according to the temper rolling ratio and is excellent in formability, and can be suitably used for automobile exterior plates.
- the yield ratio (1) represents the value measured before the temper rolling
- yield ratio (2) and yield strength, tensile strength and ductility represents the value measured after the temper rolling
- M represents martensite and B represents bainite.
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Abstract
Description
구분 | 성분조성(중량%) | |||||||||
C | Si | Mn | Cr | Mo | P | S | sol.Al | B | N | |
발명강1 | 0.025 | 0.15 | 1.75 | 0.5 | 0.04 | 0.023 | 0.006 | 0.031 | 0.0006 | 0.0031 |
발명강2 | 0.031 | 0.21 | 1.81 | 0.4 | 0.05 | 0.018 | 0.005 | 0.028 | 0.0005 | 0.0028 |
발명강3 | 0.036 | 0.18 | 1.76 | 0.3 | 0.04 | 0.023 | 0.005 | 0.024 | 0.0005 | 0.0048 |
발명강4 | 0.037 | 0.15 | 2.03 | 0.3 | 0.05 | 0.021 | 0.005 | 0.025 | 0.0012 | 0.0049 |
발명강5 | 0.052 | 0.13 | 2.16 | 0.3 | 0.05 | 0.024 | 0.005 | 0.035 | 0.0005 | 0.0045 |
비교강1 | 0.083 | 0.17 | 1.81 | 0 | 0 | 0.018 | 0.006 | 0.048 | 0 | 0.0036 |
구분 | 제조조건 | 물성 | 비고 | ||||||||||
권취온도(℃) | 냉간압하율(%) | 소둔온도(℃) | 조질압연(%) | 입계M점유비(M%) | B면적비(B%) | 전체M분율(%) | 항복비(1) | 항복강도(MPa) | 인강장도(MPa) | 연성(%) | 항복비(2) | ||
발명강1 | 553 | 62 | 782 | 0.2 | 93 | 2.5 | 3.5 | 0.44 | 251 | 492 | 33 | 0.51 | 발명예 |
557 | 61 | 785 | 0.6 | 92 | 2.3 | 3.2 | 0.44 | 275 | 500 | 32 | 0.55 | 발명예 | |
발명강2 | 556 | 62 | 779 | 0.5 | 94 | 2.1 | 2.9 | 0.43 | 273 | 506 | 32 | 0.54 | 발명예 |
563 | 63 | 743 | 0.5 | 86 | 4.8 | 2.3 | 0.55 | 312 | 495 | 34 | 0.63 | 비교예 | |
발명강3 | 652 | 62 | 821 | 1.3 | 95 | 1.8 | 4.5 | 0.44 | 323 | 513 | 31 | 0.63 | 발명예 |
651 | 63 | 823 | 1.2 | 93 | 1.9 | 4.2 | 0.43 | 308 | 497 | 33 | 0.62 | 발명예 | |
발명강4 | 482 | 61 | 835 | 0.7 | 92 | 2.6 | 1.9 | 0.44 | 331 | 581 | 27 | 0.57 | 발명예 |
485 | 63 | 855 | 0.7 | 86 | 5.2 | 12.6 | 0.62 | 329 | 522 | 30 | 0.63 | 비교예 | |
발명강5 | 648 | 76 | 835 | 1.5 | 94 | 2.1 | 3.7 | 0.42 | 318 | 505 | 31 | 0.63 | 발명예 |
645 | 75 | 836 | 1.6 | 93 | 2.2 | 3.5 | 0.43 | 321 | 502 | 32 | 0.64 | 발명예 | |
비교강1 | 556 | 58 | 786 | 0.8 | 83 | 4.8 | 11.2 | 0.58 | 335 | 540 | 29 | 0.62 | 비교예 |
552 | 58 | 789 | 0.8 | 82 | 4.6 | 13.1 | 0.57 | 329 | 522 | 27 | 0.63 | 비교예 |
Claims (8)
- 중량%로, 탄소(C): 0.01~0.08%, 망간(Mn): 1.5~2.5%, 크롬(Cr): 1.0% 이하(0%는 제외), 실리콘(Si): 1.0% 이하(0%는 제외), 인(P): 0.1% 이하(0%는 제외), 황(S): 0.01% 이하(0%는 제외), 질소(N): 0.01% 이하(0%는 제외), 산가용 알루미늄(sol.Al): 0.02~0.1%, 몰리브덴(Mo): 0.1% 이하(0%는 제외), 보론(B): 0.003% 이하(0%는 제외), 잔부 Fe 및 기타 불가피한 불순물로 이루어지고, 상기 Mn과 Cr의 중량% 합(Mn+Cr)이 1.5~3.5%를 만족하는 강판으로서,상기 강판은 주상으로 페라이트를 포함하고, 전 두께(t) 기준으로 1/4t 지점에서 미세 마르텐사이트 분율이 1~8%이고, 하기 식(1)로 정의되는 페라이트 결정립계에 존재하는 평균 입경 1㎛ 미만의 마르텐사이트의 점유비(M%)가 90% 이상이며, 하기 식(2)로 정의되는 전체 2상 조직 중 베이나이트의 면적비(B%)가 3% 이하(0% 포함)인 성형성이 우수한 복합조직강판.식(1)M(%) = {Mgb/(Mgb+Min)}×100(여기서, Mgb: 페라이트 결정립계에 존재하는 마르텐사이트 개수, Min: 페라이트 결정립내에 존재하는 마르텐사이트 개수를 나타낸다.)식(2)B(%) = {BA/(MA+BA)}×100(여기서, BA: 베이나이트 점유 면적, MA: 마르텐사이트 점유 면적을 나타낸다.)
- 제 1항에 있어서,상기 강판은 전체 미세조직 중 마르텐사이트 분율이 1~8%인 성형성이 우수한 복합조직강판.
- 제 1항에 있어서,상기 강판은 항복비(YR)가 0.45~0.6인 성형성이 우수한 복합조직강판.
- 제 1항에 있어서,상기 강판은 항복비(YR)가 0.6 초과 ~ 0.8 이하인 성형성이 우수한 복합조직강판.
- 중량%로, 탄소(C): 0.01~0.08%, 망간(Mn): 1.5~2.5%, 크롬(Cr): 1.0% 이하(0%는 제외), 실리콘(Si): 1.0% 이하(0%는 제외), 인(P): 0.1% 이하(0%는 제외), 황(S): 0.01% 이하(0%는 제외), 질소(N): 0.01% 이하(0%는 제외), 산가용 알루미늄(sol.Al): 0.02~0.1%, 몰리브덴(Mo): 0.1% 이하(0%는 제외), 보론(B): 0.003% 이하(0%는 제외), 잔부 Fe 및 기타 불가피한 불순물로 이루어지고, 상기 Mn과 Cr의 중량% 합(Mn+Cr)이 1.5~3.5%를 만족하는 강 슬라브를 재가열하는 단계;상기 재가열된 강 슬라브를 Ar3 변태점 이상에서 마무리 열간압연하여 열연강판을 제조하는 단계;상기 열연강판을 450~700℃에서 권취하는 단계;상기 권취된 열연강판을 40~80%의 압하율로 냉간압연하여 냉연강판을 제조하는 단계; 및상기 냉연강판을 연속 소둔로 또는 합금화 용융도금 연속로에서 760~850℃의 온도범위로 소둔 처리하는 단계를 포함하고,상기 소둔 처리된 강판은 주상으로 페라이트를 포함하고, 전 두께(t) 기준으로 1/4t 지점에서 미세 마르텐사이트 분율이 1~8%이고, 하기 식(1)로 정의되는 페라이트 결정립계에 존재하는 평균 입경 1㎛ 미만의 마르텐사이트의 점유비(M%)가 90% 이상이며, 하기 식(2)로 정의되는 전체 2상 조직 중 베이나이트의 면적비(B%)가 3% 이하(0% 포함)인 성형성이 우수한 복합조직강판의 제조방법.식(1)M(%) = {Mgb/(Mgb+Min)}×100(여기서, Mgb: 페라이트 결정립계에 존재하는 마르텐사이트 개수, Min: 페라이트 결정립내에 존재하는 마르텐사이트 개수를 나타낸다.)식(2)B(%) = {BA/(MA+BA)}×100(여기서, BA: 베이나이트 점유 면적, MA: 마르텐사이트 점유 면적을 나타낸다.)
- 제 5항에 있어서,상기 소둔 처리 후 조질압연하는 단계를 더 포함하는 것을 특징으로 하는 성형성이 우수한 복합조직강판의 제조방법.
- 제 6항에 있어서,상기 조질압연시 압하율이 0.85% 이하(0%는 제외)인 경우, 하기 식(3)에 의해 계산되는 값이 0.45~0.6의 범위를 만족하는 것인 성형성이 우수한 복합조직강판의 제조방법.식(3)계산 값 = (0.1699*x)+0.4545(여기서, x: 조질압하율(%)을 나타낸다.)
- 제 6항에 있어서,상기 조질압연시 압하율이 0.86~2.0%인 경우, 상기 식(3)에 의해 계산되는 값이 0.6 초과 ~ 0.8 이하의 범위를 만족하는 것인 성형성이 우수한 복합조직강판의 제조방법.
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US10538830B2 (en) | 2011-10-06 | 2020-01-21 | Nippon Steel Corporation | Steel sheet and method of producing the same |
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CN105074018A (zh) * | 2013-03-28 | 2015-11-18 | 现代制铁株式会社 | 钢板及其制备方法 |
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- 2015-11-26 JP JP2017530609A patent/JP6516845B2/ja active Active
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EP3231886A2 (en) | 2017-10-18 |
CN107109601B (zh) | 2020-03-13 |
EP3231886A4 (en) | 2017-10-18 |
WO2016093513A3 (ko) | 2017-05-18 |
CN107109601A (zh) | 2017-08-29 |
JP6516845B2 (ja) | 2019-05-22 |
EP3231886B1 (en) | 2020-03-18 |
US20170306438A1 (en) | 2017-10-26 |
KR101620750B1 (ko) | 2016-05-13 |
JP2018502992A (ja) | 2018-02-01 |
US10400301B2 (en) | 2019-09-03 |
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