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JP5034364B2 - Manufacturing method of high-strength cold-rolled steel sheet - Google Patents

Manufacturing method of high-strength cold-rolled steel sheet Download PDF

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JP5034364B2
JP5034364B2 JP2006216496A JP2006216496A JP5034364B2 JP 5034364 B2 JP5034364 B2 JP 5034364B2 JP 2006216496 A JP2006216496 A JP 2006216496A JP 2006216496 A JP2006216496 A JP 2006216496A JP 5034364 B2 JP5034364 B2 JP 5034364B2
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steel sheet
rolled steel
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裕美 吉田
金晴 奥田
俊明 占部
佳弘 細谷
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JFE Steel Corp
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Description

この発明は、自動車や電気機器などのプレス部品に有用な高強度冷延鋼板、特に、深絞り性およびプレス成形後の形状凍結性(以後、単に形状性と呼ぶ)に優れた440MPa以上の引張強度TSを有する高強度冷延鋼板の製造方法に関する。 This invention is a high-strength cold-rolled steel sheet useful for press parts such as automobiles and electrical equipment, in particular, a tensile strength of 440 MPa or more excellent in deep drawability and shape freezing property after press forming (hereinafter simply referred to as shape). the method for producing a high-strength cold-rolled steel plate having a strength TS.

近年、自動車業界においては、CO2排出規制に応じた車体軽量化と衝突時の安全性向上のための車体強化の双方が積極的に進められている。自動車車体の軽量化と強化を同時に満たすには、剛性が問題にならない範囲で部品素材を高強度化し、その板厚を薄くすることが効果的であると言われており、最近では高強度鋼板が自動車部品に積極的に使用されている。特に、軽量化効果は、より高強度の鋼板を使用するほど大きくなるため、骨格・構造部品や内・外板パネル部品に440MPa以上のTSを有する鋼板が使用される動向にある。 In recent years, in the automobile industry, both the weight reduction of the vehicle body according to the CO 2 emission regulations and the reinforcement of the vehicle body for improving safety in the event of a collision have been actively promoted. In order to satisfy the weight reduction and strengthening of automobile bodies at the same time, it is said that it is effective to increase the strength of component materials and reduce the plate thickness within a range where rigidity is not a problem. Are actively used in automotive parts. In particular, since the weight reduction effect increases as a higher strength steel plate is used, steel plates having a TS of 440 MPa or more are used for the framework / structural parts and inner / outer panel parts.

鋼板を素材とする自動車部品の多くはプレス成形によって製造されるため、鋼板には優れたプレス成形性が必要とされる。高強度鋼板を適用した場合は、特に優れた形状性(寸法精度)が要求される。そのため、従来より、高強度冷延鋼板の成形性と形状性を向上させるための技術が検討されてきた。一般に、形状性は、鋼板の降伏比YS/TS(YSは降伏強度)を低くすることで改善され、それには主としてフェライト相とマルテンサイト相を含む複合組織(Dual-Phase、DP)鋼板が有効とされている。しかしながら、DP鋼板は、概して、延性については概ね良好であり、優れた強度―延性バランス(TS×El)を有するが、伸びフランジ性(局部的な延性)や深絞り性に劣っている。   Since many automobile parts made of steel plates are manufactured by press forming, the steel plates need excellent press formability. When a high-strength steel plate is applied, a particularly excellent shape (dimensional accuracy) is required. Therefore, conventionally, techniques for improving the formability and shape of high-strength cold-rolled steel sheets have been studied. In general, the formability is improved by lowering the yield ratio YS / TS (YS is the yield strength) of the steel sheet. For this purpose, a composite structure (Dual-Phase, DP) steel sheet mainly containing a ferrite phase and a martensite phase is effective. It is said that. However, DP steel sheets are generally good in ductility and have an excellent balance between strength and ductility (TS × El), but are inferior in stretch flangeability (local ductility) and deep drawability.

深絞り性および形状性ともに優れた高強度冷延鋼板の製造方法として、例えば特許文献1には、C: 0.20%以下、Si: 1.0%以下、Mn: 0.8〜2.5%、Al: 0.01〜0.20%、N: 0.0015〜0.0150%、P: 0.10%以下を含有した鋼を熱間圧延し、冷間圧延した後、箱焼鈍と連続焼鈍の2回の熱処理を行って製造されたDP鋼板の製造方法が開示されている。また、特許文献2には、C: 0.003〜0.03%、Si: 0.2〜1%、Mn: 0.3〜1.5%、Ti: 0.02〜0.2%を含有し、原子濃度比(有効Ti)/(C+N)を0.4〜0.8にコントロールした鋼を熱間圧延し、冷間圧延した後、連続焼鈍により所定温度に加熱後急冷して深絞り性および形状性ともに優れたDP鋼板の製造方法が開示されている。ここで、有効Tiとは、全Ti濃度から酸化物と硫化物として消費されるTi濃度を除いた濃度と定義されている。   As a method for producing a high-strength cold-rolled steel sheet excellent in both deep drawability and formability, for example, in Patent Document 1, C: 0.20% or less, Si: 1.0% or less, Mn: 0.8 to 2.5%, Al: 0.01 to 0.20 %, N: 0.0015-0.0150%, P: Hot rolled steel containing 0.10% or less, cold rolled, and then manufactured DP steel sheet manufactured by performing two heat treatments: box annealing and continuous annealing A method is disclosed. Patent Document 2 contains C: 0.003 to 0.03%, Si: 0.2 to 1%, Mn: 0.3 to 1.5%, Ti: 0.02 to 0.2%, and an atomic concentration ratio (effective Ti) / (C + A method for producing a DP steel sheet having excellent deep drawability and formability is disclosed by hot rolling steel with N) controlled to 0.4 to 0.8, cold rolling, heating to a predetermined temperature by continuous annealing, and then rapidly cooling. ing. Here, effective Ti is defined as a concentration obtained by subtracting the Ti concentration consumed as oxides and sulfides from the total Ti concentration.

さらに、特許文献3には、C: 0.010〜0.050%、Si: 1.0%以下、Mn: 1.0〜3.0%、P: 0.005〜0.1%、S: 0.01%以下、Al: 0.005〜0.5%、N: 0.01%以下およびNb: 0.01〜0.3%を含有し、かつ鋼中のNbおよびCの含有量が(Nb/93)/(C/12)=0.2〜0.7を満たし、フェライト相とマルテンサイト相の量のコントロールされた深絞り性に優れたDP鋼板が開示されている。
特開昭55-100934号公報 特公平1-35900号公報 国際公開第2005/031022号パンフレット
Further, in Patent Document 3, C: 0.010 to 0.050%, Si: 1.0% or less, Mn: 1.0 to 3.0%, P: 0.005 to 0.1%, S: 0.01% or less, Al: 0.005 to 0.5%, N: 0.01% or less and Nb: 0.01 to 0.3%, and the content of Nb and C in the steel satisfies (Nb / 93) / (C / 12) = 0.2 to 0.7, and the ferrite phase and the martensite phase A DP steel sheet having a controlled amount and excellent deep drawability is disclosed.
JP 55-100934 Japanese Patent Publication No. 1-35900 International Publication No. 2005/031022 Pamphlet

しかしながら、特許文献1に記載の方法では、比較的高温で長時間の箱焼鈍工程が必要なため生産性や経済性が劣るだけではなく、鋼板同士の密着やテンパーカラーの発生などの問題がある。また、特許文献2に記載の方法では、約100℃/sの平均冷却速度で鋼板を冷却するために噴流水中に鋼板を浸漬させたり、焼鈍工程で鋼板に浸炭処理を行ったりするための特別な設備が必要となる他、鋼板を噴流水中に浸漬させるため表面処理性の問題が顕在化する。さらに、特許文献3に記載のDP鋼板では、必ずしも優れた形状性が得られない。   However, in the method described in Patent Document 1, not only productivity and economy are inferior because a long-time box annealing process is required at a relatively high temperature, but there are problems such as adhesion between steel plates and occurrence of temper color. . Further, in the method described in Patent Document 2, a special method for immersing a steel sheet in jet water to cool the steel sheet at an average cooling rate of about 100 ° C./s or carburizing the steel sheet in an annealing process. In addition to the need for such equipment, the problem of surface treatment becomes obvious because the steel sheet is immersed in the jet water. Furthermore, the DP steel sheet described in Patent Document 3 does not necessarily provide excellent shape.

本発明は、特別な工程や設備を必要とすることなく製造ができ、深絞り性および形状性ともに優れた440MPa以上のTSを有する高強度冷延鋼板の製造方法を提供することを目的とする。 The present invention aims to provide a special process or equipment can be manufactured without the need for the method of producing a high strength cold rolled steel sheet having deep drawability and 440MPa or more TS excellent in shapeability both To do.

本発明者らが、通常の工程で製造できる深絞り性および形状性ともに優れた440MPa以上のTSを有する高強度冷延鋼板について検討を進めたところ、以下の知見が得られた。   When the inventors proceeded to study a high-strength cold-rolled steel sheet having a TS of 440 MPa or more that is excellent in both deep drawability and shapeability that can be manufactured by a normal process, the following knowledge was obtained.

i)上述のごとく、従来より、プレス成形後の形状性の改善には降伏比の低減が有効であると言われているが、DP鋼板では必ずしも降伏比の低減が効果的ではなく、下記の式(2)および式(3)で定義されるδを0.3以下にすることが有効である。
δ=(σc/ρ)/TS ・・・(2)
σc={E/(1-ν2)}×t×(1/D0-1/D1) ・・・(3)
ここで、Eは鋼のヤング率(MPa)、νは鋼のポアソン比、tは鋼板の板厚(mm)、TSは鋼板の引張強度(MPa)を表し、D0は、絞り比ρで鋼板をカップ成形した後のカップの外径(mm)、D1はカップの側面部からリング試料を切り出し、鋼板の圧延方向に切れ目を入れてリング試料を開口させたときの圧延方向に対し直角方向のリングの外径(mm)を表す。ここで、σcは従来知られている残留応力の目安を示す数値であり、残留応力は加工量、材料強度の影響を受けることから、発明者らはこのσcを加工量、材料強度で規格化し、加工素材である鋼板の残留応力への寄与の目安としてδを用いた。
i) As described above, it has been conventionally said that the reduction of the yield ratio is effective for improving the formability after press forming, but the reduction of the yield ratio is not always effective in the DP steel sheet. It is effective to set δ defined by the equations (2) and (3) to 0.3 or less.
δ = (σc / ρ) / TS (2)
σc = {E / (1-ν 2 )} × t × (1 / D 0 -1 / D 1 ) (3)
Where E is steel Young's modulus (MPa), ν is steel Poisson's ratio, t is steel sheet thickness (mm), TS is steel sheet tensile strength (MPa), D 0 is drawing ratio ρ the outer diameter of the cup after the steel sheet cup shaped (mm), D 1 is perpendicular to the rolling direction when the side face of the cup cut ring sample, is opened the ring samples scored in the rolling direction of the steel sheet Represents the outer diameter (mm) of the ring in the direction. Here, σc is a numerical value indicating a conventionally known standard of residual stress. Since the residual stress is affected by the amount of processing and material strength, the inventors normalized this σc with the amount of processing and material strength. In addition, δ was used as a standard for the contribution to the residual stress of the steel sheet as the processed material.

ii)δを0.3以下にするには、C量を従来のDP鋼板に比べて少ない0.015〜0.050質量%とし、C当量より少ないNbの添加された鋼を用い、300〜650℃の温度域までの加熱速度を適切にコントロールして、フェライト相中に少量のマルテンサイト相を微細に分散させたDP鋼板とすることが効果的である。   ii) To make δ 0.3 or less, the amount of C is 0.015 to 0.050% by mass, which is smaller than that of conventional DP steel plates, and steel with Nb added less than the C equivalent is used, up to a temperature range of 300 to 650 ° C. It is effective to appropriately control the heating rate of the steel sheet to make a DP steel sheet in which a small amount of martensite phase is finely dispersed in the ferrite phase.

本発明は、このような知見に基づきなされたもので、質量%で、C: 0.015〜0.050%、Si: 1.0%以下、Mn: 1.0〜3.0%、P: 0.005〜0.1%、S: 0.01%以下、Al: 0.005〜0.5%、N: 0.01%以下、Nb: 0.01〜0.3%、および残部がFeおよび不可避的不純物からなり、NbおよびCの含有量が記の式(1)を満たす鋼スラブを、熱間圧延して熱延鋼板を製造する工程と、熱延鋼板を、400〜720℃の巻取温度で巻取る工程と、巻取り後の熱延鋼板を、冷間圧延して冷延鋼板を製造する工程と、冷延鋼板を、300〜650℃の温度域を平均加熱速度20〜70℃/sで昇温し、800〜950℃で再結晶焼鈍する工程と、再結晶焼鈍後の冷延鋼板を、800〜400℃の温度域を平均冷却速度5℃/s以上で冷却する工程とを有する、面積率で50%以上のフェライト相と面積率で1〜15%のマルテンサイト相を含むミクロ組織を有し、かつ下記の式(2)と(3)で定義されるδが0.3以下である高強度冷延鋼板の製造方法を提供する。
[C]-(12×[Nb]/93)≧0.01 ・・・(1)
δ=(σc/ρ)/TS ・・・(2)
σc={E/(1-ν 2 )}×t×(1/D 0 -1/D 1 ) ・・・(3)
ここで、[M]は元素Mの含有量(質量%)、Eは鋼のヤング率(MPa)、νは鋼のポアソン比、tは前記鋼板の板厚(mm)、TSは前記鋼板の引張強度(MPa)を表し、D 0 は、絞り比ρで前記鋼板をカップ成形した後のカップの外径(mm)、D 1 は前記カップの側面部からリング試料を切り出し、前記鋼板の圧延方向に切れ目を入れて前記リング試料を開口させたときの圧延方向に対し直角方向のリングの外径(mm)を表す。
The present invention was made based on such findings, and in mass%, C: 0.015 to 0.050%, Si: 1.0% or less, Mn: 1.0 to 3.0%, P: 0.005 to 0.1%, S: 0.01% hereinafter, Al: 0.005~0.5%, N: 0.01% or less, Nb: 0.01 to 0.3%, and balance of Fe and unavoidable impurities, the steel in which the content of Nb and C satisfy the following Symbol formula (1) Hot rolling the slab to produce a hot rolled steel sheet, winding the hot rolled steel sheet at a winding temperature of 400 to 720 ° C., and cold rolling the hot rolled steel sheet after winding. A process for producing a cold-rolled steel sheet, a process for heating the cold-rolled steel sheet at a temperature range of 300 to 650 ° C. at an average heating rate of 20 to 70 ° C./s, and performing recrystallization annealing at 800 to 950 ° C., and recrystallization And cooling the cold-rolled steel sheet after annealing at a temperature range of 800 to 400 ° C. at an average cooling rate of 5 ° C./s or more, and a ferrite phase of 50% or more in area ratio and 1 to 15% in area ratio It has a microstructure containing martensite phase and has the following formula Provided is a method for producing a high-strength cold-rolled steel sheet in which δ defined by (2) and (3) is 0.3 or less .
[C]-(12 × [Nb] / 93) ≧ 0.01 (1)
δ = (σc / ρ) / TS (2)
σc = {E / (1-ν 2 )} × t × (1 / D 0 -1 / D 1 ) (3)
Here, [M] is the content of element M (% by mass) , E is the Young's modulus (MPa) of the steel, ν is the Poisson's ratio of the steel, t is the plate thickness (mm) of the steel plate, TS is the steel plate Represents tensile strength (MPa), D 0 is the outer diameter of the cup after cup molding the steel sheet with a draw ratio ρ (mm), D 1 cut out a ring sample from the side of the cup, rolling the steel sheet It represents the outer diameter (mm) of the ring perpendicular to the rolling direction when the ring sample is opened with a cut in the direction .

上記鋼スラブには、さらに、質量%で、Mo、Cr、CuおよびNiのうちから選ばれた少なくとも1種の元素を合計で0.5%以下含有させることができる。また、さらに、質量%で、Tiを0.1%以下含有させることもできるが、その場合は、記の式(4)、および式(5)または式(6)を満たすようにする必要がある。
([Ti]/48)/([S]/32+[N]/14)≦2.0 ・・・(4)
Ti >0で、[C]-12×([Nb]/93+[ Ti ]/48)≧0.01 ・・・(5)
Ti ≦0で、[C]-12×[Nb]/93≧0.01 ・・・(6)
ここで、Ti =[Ti]-48×([N]/14+[S]/32)で、[M]は元素Mの含有量(質量%)を表す。
The steel slab can further contain at least 0.5% in total of at least one element selected from Mo, Cr, Cu, and Ni by mass%. Also, further, in mass%, although the Ti can be contained 0.1% or less, in which case, under Symbol formula (4), and it is necessary to satisfy the equation (5) or (6) .
([Ti] / 48) / ([S] / 32 + [N] / 14) ≦ 2.0 (4)
Ti * > 0, [C] -12 × ([Nb] / 93 + [Ti * ] / 48) ≧ 0.01 (5)
Ti * ≦ 0, [C] -12 × [Nb] /93≧0.01 (6)
Here, Ti * = [Ti] −48 × ([N] / 14 + [S] / 32), and [M] represents the content (mass%) of the element M.

前記再結晶焼鈍後の冷延鋼板を冷却する工程の後に、さらに冷延鋼板の表面にめっき層を形成する工程を設けることができる。   After the step of cooling the cold-rolled steel plate after the recrystallization annealing, a step of forming a plating layer on the surface of the cold-rolled steel plate can be further provided.

また、前記再結晶焼鈍後の冷延鋼板を冷却する工程に代え、前記再結晶焼鈍後の冷延鋼板を、800℃からめっき浴浸漬直前までの温度域を平均冷却速度5℃/s以上で冷却し、合金化後、合金化温度から400℃までの温度域を平均冷却速度5℃/s以上で冷却する工程としてもよい。   Further, instead of the step of cooling the cold-rolled steel sheet after the recrystallization annealing, the cold rolled steel sheet after the recrystallization annealing is performed at a temperature range from 800 ° C. to immediately before immersion in the plating bath at an average cooling rate of 5 ° C./s or more. After cooling and alloying, a temperature range from the alloying temperature to 400 ° C. may be cooled at an average cooling rate of 5 ° C./s or more.

本発明により、特別な工程や設備を必要とすることなく、深絞り性および形状性ともに優れた440MPa以上のTSを有する高強度冷延鋼板を製造できるようになった。   According to the present invention, a high-strength cold-rolled steel sheet having a TS of 440 MPa or more excellent in both deep drawability and formability can be produced without requiring a special process or equipment.

上述のように、本発明のポイントは、C量を従来のDP鋼板に比べて少ない0.015〜0.050質量%とし、C当量より少ないNbの添加された鋼を用い、300〜650℃の温度域までの加熱速度を適切にコントロールして、フェライト相中に少量のマルテンサイト相を微細に分散させてδを0.3以下にすることにより440MPa以上のTSを確保しながら深絞り性と形状性を向上させることにある。以下に、その詳細を説明する。なお、元素の含有量の単位は「質量%」であるが、以下単に「%」と記す。   As described above, the point of the present invention is that the amount of C is 0.015 to 0.050 mass%, which is smaller than that of a conventional DP steel sheet, and a steel to which Nb less than C equivalent is added is used, up to a temperature range of 300 to 650 ° C. By appropriately controlling the heating rate of the steel and finely dispersing a small amount of martensite phase in the ferrite phase to reduce δ to 0.3 or less, deep drawability and formability are improved while securing TS of 440 MPa or more. There is. The details will be described below. The unit of element content is “mass%”, but is simply referred to as “%” below.

1)成分
C: Cは、高強度化に有効であるとともに、後述のNbとともに本発明における重要な元素である。フェライト相中に少量の微細なマルテンサイト相を含む複合組織形成の観点から、その量を0.015%以上、好ましくは0.020%以上にする必要がある。しかし、その量が0.050%を超えるとフェライト粒の成長を抑制し、深絞り性などの成形性を劣化させる傾向がある。したがって、C量は0.015〜0.050%、好ましくは0.020〜0.050%に限定する。
1) ingredients
C: C is effective for increasing the strength and is an important element in the present invention together with Nb described later. From the viewpoint of forming a composite structure containing a small amount of fine martensite phase in the ferrite phase, the amount needs to be 0.015% or more, preferably 0.020% or more. However, when the amount exceeds 0.050%, the growth of ferrite grains tends to be suppressed and formability such as deep drawability tends to be deteriorated. Therefore, the amount of C is limited to 0.015 to 0.050%, preferably 0.020 to 0.050%.

Si: Siは、固溶強化の効果とともに、フェライト変態を促進させ、未変態オーステナイト中のC含有量を上昇させてフェライト相とマルテンサイト相の複合組織を形成させやすくする効果を有する。しかし、その量が1.0%を超えると熱間圧延時に赤スケールと称される表面欠陥が発生し、鋼板の表面外観を悪くする。したがって、Si量は1.0%以下に限定する。なお、溶融亜鉛めっきを施す場合には、めっきの濡れ性を悪くしてめっきむらの発生を招くので、Si量を0.7%以下にすることが望ましい。また、上記効果を得るためには、Si量を0.01%以上にすることが好ましく、0.05%以上にすることがより好ましい。   Si: In addition to the effect of solid solution strengthening, Si has the effect of accelerating ferrite transformation and increasing the C content in untransformed austenite to easily form a composite structure of ferrite phase and martensite phase. However, if the amount exceeds 1.0%, a surface defect called red scale occurs during hot rolling, which deteriorates the surface appearance of the steel sheet. Therefore, the Si content is limited to 1.0% or less. When hot dip galvanizing is performed, the wettability of the plating is deteriorated and plating unevenness is caused. Therefore, the Si content is preferably 0.7% or less. In order to obtain the above effect, the Si content is preferably 0.01% or more, and more preferably 0.05% or more.

Mn: Mnは、高強度化に有効であるととともに、マルテンサイト相が得られる臨界冷却速度を遅くする作用があり、焼鈍後の冷却時にマルテンサイト相の形成を促す。そのため、要求される強度レベルおよび焼鈍後の冷却速度に応じてその量を調整する必要がある。また、Mnは、Sによる熱間割れを防止するのに有効な元素である。このような観点から、その量を1.0%以上、好ましくは1.2%以上にする必要がある。一方、その量が3.0%を超えると成形性および溶接性を劣化させる。したがって、Mn量は1.0〜3.0%、好ましくは1.2〜3.0%に限定する。   Mn: Mn is effective in increasing the strength and has the effect of slowing down the critical cooling rate at which a martensite phase is obtained, and promotes the formation of a martensite phase during cooling after annealing. Therefore, it is necessary to adjust the amount according to the required strength level and the cooling rate after annealing. Mn is an element effective for preventing hot cracking due to S. From such a viewpoint, the amount needs to be 1.0% or more, preferably 1.2% or more. On the other hand, if the amount exceeds 3.0%, formability and weldability are deteriorated. Therefore, the amount of Mn is limited to 1.0 to 3.0%, preferably 1.2 to 3.0%.

P: Pは、固溶強化の効果を有する元素である。しかし、その量を0.005%未満にするとその効果が現れないだけでなく、脱りんコストの上昇を招く。それゆえ、その量を0.005%以上、好ましくは0.01%以上にする。一方、その量が0.1%を超えると、Pが粒界に偏析して耐二次加工脆性および溶接性を劣化させる。また、溶融亜鉛めっき後の合金化処理時に、Pはめっき層と鋼板の界面におけるFeの拡散を抑制して合金化処理性を劣化させるので、高温での合金化処理が必要となり、パウダリングやチッピング等のめっき剥離が生じやすくなる。したがって、P量は0.005〜0.1%、好ましくは0.01〜0.1%に限定する。   P: P is an element having an effect of solid solution strengthening. However, if the amount is less than 0.005%, not only the effect does not appear, but also the dephosphorization cost increases. Therefore, the amount is 0.005% or more, preferably 0.01% or more. On the other hand, if the amount exceeds 0.1%, P segregates at the grain boundaries and deteriorates secondary work embrittlement resistance and weldability. In addition, during alloying after hot dip galvanizing, P suppresses the diffusion of Fe at the interface between the plating layer and the steel sheet and degrades the alloying processability. Therefore, alloying at high temperatures is required, and powdering and Plating peeling such as chipping is likely to occur. Therefore, the P content is limited to 0.005 to 0.1%, preferably 0.01 to 0.1%.

S: Sは、熱間割れの原因になるほか、鋼中で介在物として存在して穴広げ性などの特性を劣化させる。したがって、S量は0.01%以下に限定するが、少ないほど好ましい。   S: In addition to causing hot cracking, S exists as an inclusion in steel and deteriorates properties such as hole expandability. Therefore, the amount of S is limited to 0.01% or less, but the smaller the amount, the better.

Al: Alは、鋼の脱酸元素として有用であるほか、鋼中の固溶NをAlNとして析出させ耐常温時効性を向上させる作用がある。さらに、Alはフェライト生成元素であり、(α+γ)2相温度域を調整する上でも有用である。こうした作用を発揮させるためには、その量を0.005%以上にする必要がある。一方、その量が0.5%を超えるとコスト増や表面欠陥の誘発を招く。したがって、Al量は0.005〜0.5%、好ましくは0.005〜0.1%に限定する。   Al: In addition to being useful as a deoxidizing element for steel, Al has the effect of improving the normal temperature aging resistance by precipitating solute N in the steel as AlN. Furthermore, Al is a ferrite-forming element and is useful for adjusting the (α + γ) two-phase temperature range. In order to exert such an effect, the amount needs to be 0.005% or more. On the other hand, if the amount exceeds 0.5%, cost increases and surface defects are induced. Therefore, the Al content is limited to 0.005 to 0.5%, preferably 0.005 to 0.1%.

N: 上述のように、Nが固溶Nとして存在すると耐常温時効性を劣化させる。その量が多くなると固溶Nを析出させるために多量のAlやTi添加が必要となる。したがって、N量は0.01%以下に限定するが、少ないほど好ましい。   N: As described above, when N is present as solute N, the room temperature aging resistance is deteriorated. When the amount increases, a large amount of Al or Ti is required to precipitate solid solution N. Therefore, the N content is limited to 0.01% or less, but the smaller the amount, the better.

Nb: Nbは、本発明において重要な元素の1つであり、熱間圧延後のミクロ組織を微細化したり、鋼中の固溶CをNbCとして析出させて深絞り性の向上に寄与する。このような観点から、その量を0.01%以上にする必要がある。一方、焼鈍後の冷却過程でマルテンサイト相を形成させるためには、Nbによって析出されない固溶Cを確保する必要があるが、それにはNb量を0.3%以下とし、さらにNb量をC量に応じて上記の式(1)を満たすようにコントロールする必要がある。したがって、Nb量は0.01〜0.3%に限定するとともに、上記の式(1): [C]-(12×[Nb]/93)≧0.01を満させる。   Nb: Nb is one of the important elements in the present invention, and contributes to the improvement of deep drawability by refining the microstructure after hot rolling or by precipitating solute C in steel as NbC. From such a viewpoint, the amount needs to be 0.01% or more. On the other hand, in order to form a martensite phase in the cooling process after annealing, it is necessary to ensure solid solution C that is not precipitated by Nb, but Nb content should be 0.3% or less, and Nb content should be reduced to C content. Accordingly, it is necessary to control to satisfy the above formula (1). Therefore, the Nb content is limited to 0.01 to 0.3%, and the above formula (1): [C] − (12 × [Nb] / 93) ≧ 0.01 is satisfied.

残部は、Feおよび不可避的不純物である。ここで、不可避的不純物としては、0.01%以下のSb、0.1%以下のSn、0.01%以下のZn、0.1%以下のCoなどが挙げられる。   The balance is Fe and inevitable impurities. Here, unavoidable impurities include 0.01% or less Sb, 0.1% or less Sn, 0.01% or less Zn, 0.1% or less Co, and the like.

本発明の目的を達成するには上記の成分で十分であるが、マルテンサイト相の形成を促進したり、高強度化を図るために、さらにMo、Cr、CuおよびNiのうちから選ばれた少なくとも1種の元素を合計で0.5%以下含有させることが効果的である。その量を0.5%以下にした理由は、0.5%を超えるとその効果が飽和し、コスト増を招くためである。また、その効果を得るには、その量を各々0.05%以上とすることが好ましい。   In order to achieve the object of the present invention, the above components are sufficient. However, in order to promote the formation of martensite phase or increase the strength, it was further selected from Mo, Cr, Cu and Ni. It is effective to contain at least one element in total of 0.5% or less. The reason for making the amount 0.5% or less is that when the amount exceeds 0.5%, the effect is saturated and the cost is increased. In order to obtain the effect, the amount is preferably 0.05% or more.

また、固溶N、C、SをTiN、TiC、TiS、Ti4C2S2などとして析出させて耐時効性やプレス成形性の向上を図るために、さらにTiを0.1%以下含有させ、かつ上記の式(4)、および式(5)または式(6)を満たすようにすることが効果的である。Ti量を0.1%以下、式(4)の左辺を2.0以下、および式(5)と式(6)の左辺を0.01以上にした理由は、マルテンサイト相の形成に必要な固溶Cを確保するためである。すなわち、TiはNやSと優先的に結合し、次いでCと結合するが、Ti含有量が0.1%を超えるか、あるいは([Ti]/48)/([S]/32+[N]/14)が2.0を超えると、過剰なTiにより鋼中に固溶Cを残すことが困難となる。また、Cを析出させる上で有効なTi量であるTiが、Ti>0で、[C]-12×([Nb]/93+[ Ti]/48)<0.01の場合、あるいはTi≦0で、[C]-12×[Nb]/93<0.01の場合、上記のようにマルテンサイト相形成のための固溶Cの確保が困難となる。 In addition, in order to precipitate solid solution N, C, S as TiN, TiC, TiS, Ti 4 C 2 S 2 etc. and improve aging resistance and press formability, 0.1% or less of Ti is further contained. In addition, it is effective to satisfy the above formula (4) and formula (5) or formula (6). The reason why the Ti content is 0.1% or less, the left side of Formula (4) is 2.0 or less, and the left side of Formula (5) and Formula (6) is 0.01 or more is to ensure solid solution C necessary for the formation of the martensite phase. It is to do. That is, Ti binds preferentially to N and S and then to C, but the Ti content exceeds 0.1% or ([Ti] / 48) / ([S] / 32 + [N] When / 14) exceeds 2.0, it becomes difficult to leave solute C in the steel due to excess Ti. In addition, when Ti * , which is the amount of Ti effective for precipitating C, is Ti * > 0 and [C] -12 × ([Nb] / 93 + [Ti * ] / 48) <0.01, or When Ti * ≦ 0 and [C] −12 × [Nb] / 93 <0.01, it is difficult to secure solid solution C for forming the martensite phase as described above.

なお、さらに、鋼の焼入性を向上させるBを0.003%以下の範囲で、また硫化物系介在物の形態制御に効果的なCaやREMのうち少なくとも1種の元素を0.01%以下の範囲で含有させても、本発明の効果が損なわれることはない。   In addition, B for improving the hardenability of steel is within a range of 0.003% or less, and at least one element of Ca and REM effective for shape control of sulfide inclusions is within a range of 0.01% or less. Even if it is made to contain, the effect of this invention is not impaired.

2)ミクロ組織
優れた深絞り性と440MPa以上のTSを達成するには、上記の成分に加えて、面積率で50%以上、好ましくは70〜97%のフェライト相と面積率で1〜15%、好ましくは3〜15%のマルテンサイト相を含むミクロ組織にする必要がある。フェライト相が面積率50%未満であると、良好な深絞り性を確保することが困難となる。また、マルテンサイト相が1%未満では組織強化能が低く、15%を超えると深絞り性が劣化する。ここで、フェライト相とマルテンサイト相の面積率は、鋼板の圧延方向に平行な板厚断面を光学顕微鏡あるいは走査型電子顕微鏡により観察し、観察視野中のそれぞれの相の面積率を画像処理によって求めたものである。
2) Microstructure In order to achieve excellent deep drawability and TS of 440 MPa or more, in addition to the above components, an area ratio of 50% or more, preferably 70 to 97% ferrite phase and an area ratio of 1 to 15 %, Preferably 3-15% of the martensitic phase. If the ferrite phase is less than 50%, it is difficult to ensure good deep drawability. Further, when the martensite phase is less than 1%, the structure strengthening ability is low, and when it exceeds 15%, the deep drawability deteriorates. Here, the area ratio of the ferrite phase and the martensite phase is determined by observing the plate thickness cross section parallel to the rolling direction of the steel sheet with an optical microscope or a scanning electron microscope, and calculating the area ratio of each phase in the observation field by image processing. It is what I have sought.

なお、フェライト相とマルテンサイト相の面積率の和は、必ずしも100%である必要はなく、100%未満の場合は、ベイナイト、残留オーステナイト、パーライトなどのフェライト相とマルテンサイト相以外の相が存在するが、これらのフェライト相とマルテンサイト相以外の相は少ない程好ましい。また、ここでいうフェライト相には、ポリゴナルフェライト相のほか、ベイニティックフェライト相も含まれる。   Note that the sum of the area ratios of the ferrite phase and martensite phase does not necessarily need to be 100%. If it is less than 100%, there are phases other than the ferrite phase and martensite phase such as bainite, retained austenite, and pearlite. However, the smaller the phases other than the ferrite phase and martensite phase, the better. The ferrite phase here includes not only the polygonal ferrite phase but also the bainitic ferrite phase.

3)δ
上述のように、本発明者らが検討したところによれば、プレス成形後に優れた形状性を得るには必ずしも従来から言われている降伏比の低減だけが効果的ではなく、より実際のプレス成形に近いカップ成形を行い、カップ側面から切り出したリング試料の拘束力除去後(切り目を入れた後)の外径変化より求まる上記の式(2)と式(3)で定義されたδを小さくすることが効果的であり、δを0.3以下とすれば実プレスで寸法精度に問題が生じることが格段に少なくなることが明らかになった。
3) δ
As described above, according to the study by the present inventors, it is not always effective to reduce the yield ratio, which has been said so far, in order to obtain excellent shape after press molding. Perform cup molding close to molding, and define δ defined by the above formula (2) and formula (3) obtained from the change in outer diameter after removing the restraining force of the ring sample cut from the cup side surface (after making a cut) It has become clear that it is effective to make it smaller, and that if δ is 0.3 or less, the problem of dimensional accuracy in the actual press will be remarkably reduced.

なお、マルテンサイト相の面積率や降伏比がほぼ同じでも、δが0.3を超えると実プレスの寸法精度が悪くなる場合があることから、形状性にはマルテンサイト相の形態や分布が大きく影響していると推察される。δを0.3以下でより小さくするには、マルテンサイト相の平均面積を6μm2以下にし、かつ全マルテンサイト相のうち扁平率が2以下のマルテンサイト相を70%以上存在させることが好ましい。 Even if the area ratio and yield ratio of the martensite phase are almost the same, if δ exceeds 0.3, the dimensional accuracy of the actual press may deteriorate. It is inferred that In order to make δ smaller at 0.3 or less, it is preferable that the average area of the martensite phase is 6 μm 2 or less, and 70% or more of the martensite phase having an aspect ratio of 2 or less is present among all martensite phases.

上記成分とミクロ組織を有し、δが0.3以下の高強度冷延鋼板の表面には、電気めっき法あるいは溶融めっき法などにより、純亜鉛、亜鉛系合金、純Al、Al系合金などのめっき層を設けることができる。 The surface of a high-strength cold-rolled steel sheet having the above components and microstructure and having a δ of 0.3 or less is plated with pure zinc, zinc-based alloy, pure Al, Al-based alloy, etc. by electroplating or hot dipping. A layer can be provided.

4)製造方法
上記ミクロ組織を有し、δが0.3以下の高強度冷延鋼板は、上記した成分を有する鋼スラブを、熱間圧延して熱延鋼板を製造する工程と、熱延鋼板を、400〜720℃の巻取温度で巻取る工程と、巻取り後の熱延鋼板を、冷間圧延して冷延鋼板を製造する工程と、冷延鋼板を、300〜650℃の温度域を平均加熱速度18〜70℃/sで昇温し、800〜950℃で再結晶焼鈍する、あるいは300〜650℃の温度域を平均加熱速度3℃/s以上18℃/s未満で昇温後、650〜800℃の温度域を平均加熱速度1〜7℃/sで昇温し、800〜950℃で再結晶焼鈍する工程と、再結晶焼鈍後の冷延鋼板を、800〜400℃の温度域を平均冷却速度5℃/s以上で冷却する工程とを有する高強度冷延鋼板の製造方法により製造できる。
4) Manufacturing method
A high-strength cold-rolled steel sheet having the above microstructure and δ of 0.3 or less is a step of hot-rolling a steel slab having the above-described components to produce a hot-rolled steel sheet, The process of winding at a coiling temperature of ℃, the process of cold-rolling the hot-rolled steel sheet after winding, and manufacturing the cold-rolled steel sheet, the average temperature of the cold-rolled steel sheet in the temperature range of 300-650 ℃ The temperature is raised at 18 to 70 ° C./s, and recrystallization annealing is performed at 800 to 950 ° C., or the temperature range of 300 to 650 ° C. is raised at an average heating rate of 3 ° C./s to less than 18 ° C./s, and then 650 to The temperature range of 800 ° C is increased at an average heating rate of 1 to 7 ° C / s, and the recrystallization annealing process at 800 to 950 ° C and the cold rolled steel sheet after the recrystallization annealing are performed at a temperature range of 800 to 400 ° C. It can be produced by a method for producing a high-strength cold-rolled steel sheet having a step of cooling at an average cooling rate of 5 ° C./s or more.

本発明の製造方法で使用する鋼スラブは、成分のマクロ偏析を防止すべく連続鋳造法(薄スラブ鋳造法も含む)で製造することが望ましいが、造塊法で製造してもよい。また、スラブを熱間圧延するには、鋼スラブをいったん室温まで冷却し、その後再加熱して圧延する従来法に加え、連続鋳造後直ちに熱間圧延する方法、あるいは室温まで冷却せず温片のままで加熱炉に装入し圧延する方法などの省エネルギープロセスも問題なく適用できる。   The steel slab used in the production method of the present invention is desirably produced by a continuous casting method (including a thin slab casting method) in order to prevent macro segregation of components, but may be produced by an ingot-making method. Also, in order to hot-roll the slab, in addition to the conventional method in which the steel slab is once cooled to room temperature and then reheated and rolled, a method of hot rolling immediately after continuous casting, or a hot piece without cooling to room temperature. An energy saving process such as a method of charging and rolling in a heating furnace as it is can be applied without any problem.

スラブ加熱温度は、熱間圧延時に圧延荷重が増大し、トラブル発生の危険性が増大しなように1000℃以上に、また酸化重量の増加に伴うスケールロスの増大を防止するために1300℃以下とすることが好適である。   The slab heating temperature is 1000 ° C or higher so that the rolling load increases during hot rolling and the risk of troubles does not increase, and 1300 ° C or lower to prevent an increase in scale loss due to an increase in oxidized weight. Is preferable.

加熱後のスラブは、粗圧延によりシートバーとされる。粗圧延の条件は、特に規定されず、常法に従って行えばよい。また、スラブの加熱温度を低く目にした場合は、圧延時のトラブルを防止するといった観点から、シートバーヒーターを活用してシートバーを加熱することが好ましい。   The slab after heating is made into a sheet bar by rough rolling. The conditions for rough rolling are not particularly limited, and may be performed according to a conventional method. When the heating temperature of the slab is low, it is preferable to heat the sheet bar using a sheet bar heater from the viewpoint of preventing troubles during rolling.

シートバーは、仕上圧延により熱延板とされる。このとき、圧延時の負荷が高くならないように仕上温度FTは、800℃以上にすることが好ましい。また、圧延荷重を低減したり、鋼板の形状や特性の均一化を図るために、仕上圧延の一部または全部のパス間で潤滑圧延を行うことができる。潤滑圧延時の摩擦係数は0.10〜0.25の範囲にすることが好ましい。さらに、熱間圧延の操業安定性の観点から、シートバー同士を接合して連続的に圧延する連続圧延プロセスを適用することが好ましい。   The sheet bar is a hot-rolled sheet by finish rolling. At this time, the finishing temperature FT is preferably 800 ° C. or higher so that the load during rolling does not increase. Further, in order to reduce the rolling load and to make the shape and characteristics of the steel sheet uniform, lubrication rolling can be performed between some or all passes of finish rolling. The coefficient of friction during lubrication rolling is preferably in the range of 0.10 to 0.25. Furthermore, from the viewpoint of operational stability of hot rolling, it is preferable to apply a continuous rolling process in which sheet bars are joined and continuously rolled.

熱間圧延後の巻取温度CTは、NbCを析出させるために400〜720℃、好ましくは550〜680℃にする。なお、CTが720℃を超えると熱延板の結晶粒が粗大化し、その結果、冷延焼鈍後の組織も粗大化しやすくなり、強度低下や表面性状の劣化を招くことがある。また、CTが400℃未満ではNbCの析出が起こりにくく、深絞り性を確保することが困難になる。   The coiling temperature CT after hot rolling is 400 to 720 ° C, preferably 550 to 680 ° C, in order to precipitate NbC. In addition, when CT exceeds 720 ° C., the crystal grains of the hot-rolled sheet become coarse, and as a result, the structure after cold-rolling annealing tends to become coarse, which may lead to a decrease in strength and deterioration of surface properties. Further, when CT is less than 400 ° C., NbC is hardly precipitated and it is difficult to ensure deep drawability.

熱延鋼板は、酸洗によりスケールを除去した後、冷間圧延により冷延鋼板とされる。圧延時の圧下率は、深絞り性の向上の観点から少なくとも40%以上とすることが好ましく、50%以上とすることがより好ましい。   A hot-rolled steel sheet is made into a cold-rolled steel sheet by cold rolling after removing scales by pickling. The rolling reduction during rolling is preferably at least 40% or more, more preferably 50% or more, from the viewpoint of improving deep drawability.

冷延鋼板は、300〜650℃の温度域を平均加熱速度18〜70℃/sで昇温し、800〜950℃で再結晶焼鈍される、あるいは300〜650℃の温度域を平均加熱速度3℃/s以上18℃/s未満で昇温後、650〜800℃の温度域を平均加熱速度1〜7℃/sで昇温し、800〜950℃で再結晶焼鈍される。300〜650℃の温度域における加熱速度および650〜800℃の温度域における加熱速度は、本発明のポイントの一つである。   Cold rolled steel sheet is heated at an average heating rate of 18 to 70 ° C / s in the temperature range of 300 to 650 ° C and recrystallized at 800 to 950 ° C, or the average heating rate in the temperature range of 300 to 650 ° C. After the temperature is increased at 3 ° C./s or more and less than 18 ° C./s, the temperature range of 650 to 800 ° C. is increased at an average heating rate of 1 to 7 ° C./s, and recrystallization annealing is performed at 800 to 950 ° C. The heating rate in the temperature range of 300 to 650 ° C and the heating rate in the temperature range of 650 to 800 ° C are one of the points of the present invention.

図1に、C: 0.025%、Si: 0.5%、Mn: 2.0%、P: 0.035%、S: 0.005%以下、Al: 0.03%、N: 0.002%、Nb: 0または0.08%の成分を有する鋼を用い、300〜650℃の温度域における平均加熱速度を0.01〜70℃/sに、650〜800℃の温度域における平均加熱速度を0.3℃/sと3℃/sに変えて連続焼鈍(焼鈍温度: 850℃)してDP鋼板(板厚: 1.2mm)を製造し、δを求めた結果を示す。なお、ここで、形状性の指標であるδは、ブランク径が68mmの鋼板を打ち抜き、径が33mmのポンチを用い、ダイ肩Rが2.5mm、しわ押さえ力が10kN、絞り速度が10mm/min、絞り比(ブランク径/ポンチ径)が2.06の条件で、ダイ側を潤滑油およびテフロン(登録商標)シートで潤滑してカップ成形し、カップ底部から高さ8mmの位置より幅10mmのリング試料を放電加工により切り出し、鋼板の圧延方向に切れ目を入れて開口させ、圧延方向に対し直角方向のリングの外径を測定し、ヤング率E: 210GPa(=210×103MPa)、ポアソン比ν: 0.3として上記の式(2)と式(3)から求めたものである。また、鋼板の組織は、板厚1/4部付近を2000倍で観察したSEM写真を用い、マルテンサイト相の面積率、扁平率、平均面積を測定した。なお、マルテンサイト相の平均面積は、以下の式より求めた。
マルテンサイト相の平均面積=[観察視野におけるマルテンサイト相の面積率(%)]×[観察視野の面積(μm2)]/[観察視野において観察されたマルテンサイト相の個数]
図1に示すように、300〜650℃の温度域の平均加熱速度を18〜70℃/s、好ましくは20〜70℃/sにすることによりδを0.3以下にでき、優れた形状性が得られる。C量とNb量を上述のように調整することで、従来DP鋼に比べ、マルテンサイト相の面積率が若干低めとなり、さらにその少量のマルテンサイト相が微細に得られることにより、形状性をよくしているものと考えられる。特に、300〜650℃の温度域における加熱速度を速めることにより、その傾向が顕著になっているようである。また、650〜800℃の平均加熱速度が1〜7℃/sで昇温すると、更に形状性が良好であるが、これは、マルテンサイト相のうち扁平率が2以下のものが70%以上となり、マルテンサイト相の平均面積も6μm2以下となってマルテンサイトの微細均一化が進行したためと推定される。特に、Nb添加による再結晶遅延がその後の2相域焼鈍におけるα-γ変態に何らかの影響を及ぼした結果と推測されるが、詳細は不明である。なお、平均加熱速度は、70℃/sを超えると設備への負荷が大きくなるので、70℃/s以下、好ましくは50℃/s以下とする。
Figure 1 has components of C: 0.025%, Si: 0.5%, Mn: 2.0%, P: 0.035%, S: 0.005% or less, Al: 0.03%, N: 0.002%, Nb: 0 or 0.08% Continuous annealing using steel, changing the average heating rate in the temperature range of 300-650 ° C to 0.01-70 ° C / s, and changing the average heating rate in the temperature range of 650-800 ° C to 0.3 ° C / s and 3 ° C / s (Annealing temperature: 850 ° C.) A DP steel sheet (sheet thickness: 1.2 mm) was produced, and the results of determining δ are shown. Here, δ, which is an index of shape, is a punched steel plate with a blank diameter of 68 mm, a punch with a diameter of 33 mm, a die shoulder R of 2.5 mm, a wrinkle holding force of 10 kN, and a drawing speed of 10 mm / min. , Under the condition that the drawing ratio (blank diameter / punch diameter) is 2.06, the die side is lubricated with lubricating oil and Teflon (registered trademark) sheet to form a cup, and the ring sample is 10mm wide from the 8mm height from the bottom of the cup. Is cut by electric discharge machining, opened in the rolling direction of the steel sheet, measured the outer diameter of the ring perpendicular to the rolling direction, Young's modulus E: 210GPa (= 210 × 10 3 MPa), Poisson's ratio ν : 0.3 and obtained from the above formulas (2) and (3). Moreover, the structure of the steel sheet was measured for the area ratio, the flatness ratio, and the average area of the martensite phase by using an SEM photograph in which the vicinity of the thickness of 1/4 part was observed at 2000 times. In addition, the average area of the martensite phase was calculated | required from the following formula | equation.
Average area of martensite phase = [area ratio of martensite phase in observation field (%)] × [area of observation field (μm 2 )] / [number of martensite phases observed in observation field]
As shown in FIG. 1, by setting the average heating rate in the temperature range of 300 to 650 ° C. to 18 to 70 ° C./s, preferably 20 to 70 ° C./s, δ can be reduced to 0.3 or less, and excellent shape characteristics are obtained. can get. By adjusting the amount of C and Nb as described above, the area ratio of the martensite phase is slightly lower than that of conventional DP steel, and the small amount of martensite phase can be obtained finely, thereby reducing the shape. It seems to be doing well. In particular, the tendency seems to be remarkable by increasing the heating rate in the temperature range of 300 to 650 ° C. In addition, when the average heating rate at 650 to 800 ° C. is raised at 1 to 7 ° C./s, the shape is further improved. This is because the martensite phase has an aspect ratio of 2 or less and 70% or more. Therefore, it is presumed that the average area of the martensite phase was 6 μm 2 or less, and the martensite was finely homogenized. In particular, it is speculated that the recrystallization delay due to Nb addition had some effect on the α-γ transformation in the subsequent two-phase annealing, but the details are unknown. If the average heating rate exceeds 70 ° C./s, the load on the equipment increases, so it is 70 ° C./s or less, preferably 50 ° C./s or less.

また、図1に示すように、300〜650℃の温度域の平均加熱速度が18℃/sに満たない場合でも、3℃/s以上であれば、引続く650〜800℃の温度域を平均加熱速度1〜7℃/sで昇温することにより良好な形状性が得られる。これは、300〜650℃の温度域の平均加熱速度が3℃/s以上18℃/s未満でも650〜800℃の温度域の平均加熱速度を1〜7℃/sで昇温することにより、均一で微細なマルテンサイト相が形成されるためと考えられる。   In addition, as shown in FIG. 1, even when the average heating rate in the temperature range of 300 to 650 ° C is less than 18 ° C / s, if the average heating rate is 3 ° C / s or more, the subsequent temperature range of 650 to 800 ° C is maintained. Good shape properties can be obtained by raising the temperature at an average heating rate of 1 to 7 ° C./s. This is because even if the average heating rate in the temperature range of 300 to 650 ° C is 3 ° C / s or more and less than 18 ° C / s, the average heating rate in the temperature range of 650 to 800 ° C is increased by 1 to 7 ° C / s. This is probably because a uniform and fine martensite phase is formed.

300〜650℃の温度域の平均加熱速度が3℃/s未満では、δが0.3を超えて形状性が劣化しており、これは、徐加熱焼鈍することで冷却後の組織で、フェライト分率が低下し、加えてマルテンサイト相が粗大化する傾向があるためと考えられる。300〜650℃の温度域を3℃/s以上18℃/s未満の平均加熱速度で昇温する場合、650〜800℃の温度域の平均加熱速度を1℃/s未満とすると、これを助長することになり、また650〜800℃の温度域の平均加熱速度が7℃/sを超えると、再結晶粒の成長を妨げr値が1.2未満に低下することになり、好ましくない。このため、300〜650℃の温度域を3℃/s以上18℃/s未満の平均加熱速度で昇温する場合には、650〜800℃の温度域の平均加熱速度を1〜7℃/sとする。   When the average heating rate in the temperature range of 300 to 650 ° C. is less than 3 ° C./s, δ exceeds 0.3 and the shape is deteriorated. This is the structure after cooling by slow heating annealing, and the ferrite content This is considered to be due to the fact that the ratio decreases and the martensite phase tends to become coarse. When heating the temperature range of 300-650 ° C at an average heating rate of 3 ° C / s or more and less than 18 ° C / s, if the average heating rate of the temperature range of 650-800 ° C is less than 1 ° C / s, If the average heating rate in the temperature range of 650 to 800 ° C. exceeds 7 ° C./s, the growth of recrystallized grains is hindered and the r value is reduced to less than 1.2, which is not preferable. For this reason, when the temperature range of 300 to 650 ° C. is increased at an average heating rate of 3 ° C./s or more and less than 18 ° C./s, the average heating rate of the temperature range of 650 to 800 ° C. is 1 to 7 ° C. / s.

焼鈍温度は、再結晶温度以上で、冷却後にフェライト相とマルテンサイト相を含む組織が得られる(α+γ)2相域温度以上とするため、800℃以上にする。しかし、950℃を超えると、再結晶粒が著しく粗大化し、機械的特性および表面性状が著しく劣化する。また、特に限定するものではないが、再結晶粒を十分に発達させて深絞り性や穴広げ性を向上させるために、300〜650℃の温度域を平均加熱速度18〜70℃/sで昇温させた場合には、700℃〜焼鈍温度の温度域は徐加熱、好ましくは5℃/s以下の加熱速度で加熱することが望ましい。また、800〜950℃の焼鈍温度で1〜300秒間保持することが好ましい。これは、保持時間を1秒間以上にすることにより、再結晶が十分に進行するとともに、(α+γ)2相域において相分離と固溶Cのオーステナイト相への濃化が十分に促進されるためである。なお、保持時間は、10秒間以上とすることがより好ましい。一方、保持時間が300秒間を超えると結晶粒が粗大化し、強度や表面性状など諸特性が劣化する傾向にある。   The annealing temperature is set to 800 ° C. or higher in order to set the annealing temperature to the recrystallization temperature or higher and to the (α + γ) two-phase region temperature or higher at which a structure including a ferrite phase and a martensite phase is obtained after cooling. However, when the temperature exceeds 950 ° C., the recrystallized grains are remarkably coarsened, and the mechanical properties and surface properties are remarkably deteriorated. Further, although not particularly limited, in order to sufficiently develop the recrystallized grains and improve the deep drawability and hole expansibility, the temperature range of 300 to 650 ° C is set at an average heating rate of 18 to 70 ° C / s. When the temperature is raised, it is desirable that the temperature range from 700 ° C. to the annealing temperature is heated gradually, preferably at a heating rate of 5 ° C./s or less. Moreover, it is preferable to hold | maintain for 1 to 300 second at the annealing temperature of 800-950 degreeC. This is because when the holding time is set to 1 second or longer, recrystallization proceeds sufficiently and phase separation and concentration of solute C into the austenite phase is sufficiently promoted in the (α + γ) 2 phase region. Because. The holding time is more preferably 10 seconds or longer. On the other hand, when the holding time exceeds 300 seconds, the crystal grains become coarse and various properties such as strength and surface properties tend to deteriorate.

焼鈍後の冷却速度は、マルテンサイト相の形成の観点から800〜400℃の温度域を平均冷却速度5℃/s以上で冷却する必要がある。なお、このような冷却速度を確保するためには、焼鈍を連続焼鈍ラインで行うことが好ましい。冷却速度規定の開始温度を800℃とした理由は、マルテンサイト相を得るため(α+γ)2相域から冷却を開始する必要があるためである。したがって、800℃以上の焼鈍温度から5℃/s以上の冷却速度で冷却しても何ら問題はない。   As for the cooling rate after annealing, it is necessary to cool a temperature range of 800 to 400 ° C. at an average cooling rate of 5 ° C./s or more from the viewpoint of forming a martensite phase. In addition, in order to ensure such a cooling rate, it is preferable to perform annealing in a continuous annealing line. The reason why the start temperature specified by the cooling rate is set to 800 ° C. is that it is necessary to start cooling from the (α + γ) 2 phase region in order to obtain a martensite phase. Therefore, there is no problem even if cooling is performed at a cooling rate of 5 ° C./s or higher from an annealing temperature of 800 ° C. or higher.

また、冷却速度規定の終了温度を400℃としたのは、マルテンサイト相を得る上で800℃から400℃の温度域での冷却速度の影響が大きいためである。したがって、少なくとも400℃まで5℃/s以上で冷却すればよく、400℃まで冷却後は、そのまま冷却を続けてもよいし、400〜200℃の温度域での一定時間保持後冷却してもよい。保持する場合は、生成したマルテンサイト相の軟質化が起こらないように、また製造コスト増とならないように、保持時間を600秒間以下にすることが好ましい。   The reason why the end temperature for regulating the cooling rate is set to 400 ° C. is that the influence of the cooling rate in the temperature range from 800 ° C. to 400 ° C. is large in obtaining the martensite phase. Therefore, it is sufficient to cool at least 5 ° C / s to 400 ° C. After cooling to 400 ° C, the cooling may be continued as it is, or it may be cooled after holding for a certain time in the temperature range of 400 to 200 ° C. Good. In the case of holding, it is preferable that the holding time is 600 seconds or less so that the generated martensite phase does not soften and the manufacturing cost does not increase.

冷却後の鋼板には、上述したように、電気めっき処理、あるいは溶融めっき処理などによりめっき層を形成することができる。なお、オンラインで合金化溶融亜鉛めっきを施す場合は、マルテンサイト相の形成の観点から、前記800〜950℃での焼鈍後、800℃からめっき浴浸漬直前までの温度域を平均5℃/s以上で冷却し、合金化後、合金化温度から400℃までを平均5℃/s以上で冷却することが好ましい。このとき、めっき浴浸漬直前の鋼板温度は概ね480〜520℃、めっき浴温度は概ね440〜480℃であり、合金化温度は概ね500〜600℃である。また、このようにして製造された冷延鋼板あるいはめっき鋼板には、形状矯正、表面粗度調整の目的で調質圧延またはレベラー加工を施してもよい。調質圧延あるいはレべラー加工の伸び率は合計で0.2〜15%の範囲内であることが好ましい。これは、0.2%未満では、形状矯正や表面粗度調整の目的が達成できないおそれがあり、15%を超えると顕著な延性低下をもたらす傾向があるためである。   As described above, a plated layer can be formed on the cooled steel sheet by electroplating or hot dipping. In addition, when performing alloying hot dip galvanization online, from the viewpoint of forming a martensite phase, the average temperature range from 800 ° C. to just before immersion in the plating bath is 5 ° C./s after annealing at 800 to 950 ° C. After cooling and alloying, it is preferable to cool from the alloying temperature to 400 ° C. at an average of 5 ° C./s or more. At this time, the steel plate temperature immediately before immersion in the plating bath is approximately 480 to 520 ° C., the plating bath temperature is approximately 440 to 480 ° C., and the alloying temperature is approximately 500 to 600 ° C. In addition, the cold-rolled steel sheet or the plated steel sheet thus manufactured may be subjected to temper rolling or leveler processing for the purpose of shape correction and surface roughness adjustment. The total elongation of temper rolling or leveler processing is preferably in the range of 0.2 to 15%. This is because if it is less than 0.2%, the purpose of shape correction and surface roughness adjustment may not be achieved, and if it exceeds 15%, there is a tendency to cause a significant decrease in ductility.

表1に示す組成の鋼A〜Nを転炉で溶製し、連続鋳造法でスラブとした。これらスラブを1250℃に加熱後、粗圧延してシートバーとし、次いで仕上温度860℃で仕上圧延して熱延板とし、巻取温度650℃で巻取った。これらの熱延板を酸洗後圧下率65%で冷間圧延して冷延板とし、引続き、連続焼鈍ラインにて表2に示す条件で連続焼鈍を行い、伸び率0.5%の調質圧延を施して鋼板No.1、2、4〜18の試料を作製した。なお、300〜650℃の温度域における加熱速度は、ラインスピードを変えて変化させた。また、鋼板No.3は、連続溶融亜鉛めっきライン(CGL)にて焼鈍後オンラインでめっき処理を施した試料であり、めっき浴浸漬直前の板温は500℃、めっき浴温度は460℃、合金化温度は550℃である。そして、得られた試料について、上述の方法でミクロ組織を評価し、次の方法で形状性と引張特性を評価した。   Steels A to N having the compositions shown in Table 1 were melted in a converter and made into slabs by a continuous casting method. These slabs were heated to 1250 ° C., roughly rolled into sheet bars, then finish rolled at a finishing temperature of 860 ° C. to form hot rolled sheets, and wound at a winding temperature of 650 ° C. These hot-rolled sheets are pickled and cold-rolled at a rolling reduction of 65% to obtain cold-rolled sheets. Subsequently, continuous annealing is performed in the continuous annealing line under the conditions shown in Table 2, and temper rolling with an elongation of 0.5%. The steel plates No. 1, 2, and 4 to 18 were prepared. The heating rate in the temperature range of 300 to 650 ° C. was changed by changing the line speed. Steel plate No. 3 is a sample that has been plated online after annealing in a continuous hot dip galvanizing line (CGL). The plate temperature immediately before immersion in the plating bath is 500 ° C, the plating bath temperature is 460 ° C, and the alloy The conversion temperature is 550 ° C. And about the obtained sample, the microstructure was evaluated by the above-mentioned method, and the formability and the tensile characteristic were evaluated by the following method.

形状性δ:ブランク径が68mmの鋼板を打ち抜き、径が33mmのポンチを用い、ダイ肩Rが2.5mm、しわ押さえ力が10kN、絞り速度が10mm/min、絞り比(ブランク径/ポンチ径)が2.06の条件で、ダイ側を潤滑油およびテフロン(登録商標)シートで潤滑してカップ成形し、カップ底部から高さ8mmの位置より幅10mmのリング試料を放電加工により切り出し、鋼板の圧延方向に切れ目を入れて開口させ、圧延方向に対し直角方向のリングの外径を測定し、上記の式(2)と式(3)から求めた。このとき、ヤング率Eは210GPa(=210×103MPa)、ポアソン比νは0.3として計算した。また、板厚tは1.2mmであった。 Formability δ: A steel plate with a blank diameter of 68 mm is punched, a punch with a diameter of 33 mm is used, the die shoulder R is 2.5 mm, the wrinkle holding force is 10 kN, the drawing speed is 10 mm / min, the drawing ratio (blank diameter / punch diameter) However, under the condition of 2.06, the die side is lubricated with lubricating oil and a Teflon (registered trademark) sheet to form a cup, and a ring sample having a width of 10 mm is cut from the bottom of the cup at a height of 8 mm by electric discharge machining. The outer diameter of the ring in the direction perpendicular to the rolling direction was measured and determined from the above formulas (2) and (3). At this time, the Young's modulus E was calculated to be 210 GPa (= 210 × 10 3 MPa) and the Poisson's ratio ν was 0.3. The plate thickness t was 1.2 mm.

引張特性値:試料から圧延方向に対して90°方向にJIS5号引張試験片を採取し、JIS Z 2241の規定に準拠してクロスヘッド速度10mm/min一定で引張試験を行い、YS、TS、YR、伸び(El)、r値を求めた。   Tensile property value: JIS No. 5 tensile test specimen is taken from the sample in the direction of 90 ° to the rolling direction, and the tensile test is performed at a constant crosshead speed of 10 mm / min in accordance with the provisions of JIS Z 2241. YS, TS, YR, elongation (El), and r value were determined.

r値の測定は、試料から、圧延方向、圧延方向に対し45°方向、圧延方向に対し90°方向からJIS5号引張試験片を採取し、10%の単軸引張歪を付与した時の各試験片の幅歪と板厚歪を測定し、JIS S 2254の規定に準拠して平均r値(平均塑性歪比)を以下の式から算出し、深絞り性を評価した。
平均r値=(r0+2r45+r90)/4
ここで、r0、r45、r90は、それぞれ圧延方向に対し0°、45°、90°方向から採取した試験片で測定した塑性歪比である。
The r value was measured by taking a JIS No. 5 tensile specimen from the sample in the rolling direction, 45 ° direction with respect to the rolling direction and 90 ° direction with respect to the rolling direction, and applying 10% uniaxial tensile strain. The width strain and the plate thickness strain of the test piece were measured, and the average r value (average plastic strain ratio) was calculated from the following formula in accordance with the provisions of JIS S 2254 to evaluate deep drawability.
Average r value = (r 0 + 2r 45 + r 90 ) / 4
Here, r 0, r 45, and r 90 are plastic strain ratios measured with test pieces taken from 0 °, 45 °, and 90 ° directions with respect to the rolling direction, respectively.

組織:圧延方向の板厚断面を鏡面研磨後、1.5%Nital腐食を施し、SEMで板厚1/4付近を2000倍で観察したSEM写真を用い、マルテンサイト相とフェライト相についてそれぞれの相の面積率を求めた。また、マルテンサイト相は扁平率2以下の割合と平均面積を定量評価した。なお、マルテンサイト相の平均面積は、3視野ついて以下の式より求め、平均した。
マルテンサイト相の平均面積=[観察視野におけるマルテンサイト相の面積率(%)]×[観察視野の面積(μm2)]/[観察視野において観察されたマルテンサイト相の個数]
結果を表3に示す。鋼板No.1〜3、5〜10、16〜18の本発明例では、いずれもTSが440MPa以上、平均r値が1.2以上、δが0.3以下であり、深絞り性および形状性ともに優れた高強度冷延鋼板が得られる。
Microstructure: After the mirror thickness of the sheet thickness section in the rolling direction, 1.5% Nital corrosion was applied, and SEM photographs were used to observe the thickness around 1/4 with SEM at 2000 times. The area ratio was determined. In addition, the martensite phase was quantitatively evaluated for the ratio of the flatness ratio of 2 or less and the average area. The average area of the martensite phase was obtained from the following formula for the three fields of view and averaged.
Average area of martensite phase = [area ratio of martensite phase in observation field (%)] × [area of observation field (μm 2 )] / [number of martensite phases observed in observation field]
The results are shown in Table 3. Steel sheet Nos. 1 to 3, 5 to 10, and 16 to 18 are all examples of the present invention, TS is 440 MPa or more, average r value is 1.2 or more, and δ is 0.3 or less, and both deep drawability and shape are excellent. A high-strength cold-rolled steel sheet is obtained.

Figure 0005034364
Figure 0005034364

Figure 0005034364
Figure 0005034364

Figure 0005034364
Figure 0005034364

本発明の製造方法で製造された高強度冷延鋼板は、自動車部品に限らず、家電部品やパイプ用素材としても適用可能である。 The high-strength cold-rolled steel sheet manufactured by the manufacturing method of the present invention is applicable not only to automobile parts but also to home appliance parts and pipe materials.

焼鈍時の300〜650℃における平均加熱速度とδとの関係を示す図である。It is a figure which shows the relationship between the average heating rate in 300-650 degreeC at the time of annealing, and (delta).

Claims (5)

質量%で、C: 0.015〜0.050%、Si: 1.0%以下、Mn: 1.0〜3.0%、P: 0.005〜0.1%、S: 0.01%以下、Al: 0.005〜0.5%、N: 0.01%以下、Nb: 0.01〜0.3%、および残部がFeおよび不可避的不純物からなり、NbおよびCの含有量が下記の式(1)を満たす鋼スラブを、熱間圧延して熱延鋼板を製造する工程と、
前記熱延鋼板を、400〜720℃の巻取温度で巻取る工程と、
前記巻取り後の熱延鋼板を、冷間圧延して冷延鋼板を製造する工程と、
前記冷延鋼板を、300〜650℃の温度域を平均加熱速度20〜70℃/sで昇温し、800〜950℃で再結晶焼鈍する工程と、
前記再結晶焼鈍後の冷延鋼板を、800〜400℃の温度域を平均冷却速度5℃/s以上で冷却する工程と、
を有する、面積率で50%以上のフェライト相と面積率で1〜15%のマルテンサイト相を含むミクロ組織を有し、かつ下記の式(2)と(3)で定義されるδが0.3以下である高強度冷延鋼板の製造方法;
[C]-(12×[Nb]/93)≧0.01 ・・・(1)
δ=(σc/ρ)/TS ・・・(2)
σc={E/(1-ν 2 )}×t×(1/D 0 -1/D 1 ) ・・・(3)
ここで、[M]は元素Mの含有量(質量%)、Eは鋼のヤング率(MPa)、νは鋼のポアソン比、tは前記鋼板の板厚(mm)、TSは前記鋼板の引張強度(MPa)を表し、D 0 は、絞り比ρで前記鋼板をカップ成形した後のカップの外径(mm)、D 1 は前記カップの側面部からリング試料を切り出し、前記鋼板の圧延方向に切れ目を入れて前記リング試料を開口させたときの圧延方向に対し直角方向のリングの外径(mm)を表す。
In mass%, C: 0.015-0.050%, Si: 1.0% or less, Mn: 1.0-3.0%, P: 0.005-0.1%, S: 0.01% or less, Al: 0.005-0.5%, N: 0.01% or less, Nb: 0.01 to 0.3%, and the balance is made of Fe and inevitable impurities, and a steel slab in which the content of Nb and C satisfies the following formula (1) is hot-rolled to produce a hot-rolled steel sheet: ,
Winding the hot-rolled steel sheet at a winding temperature of 400 to 720 ° C .;
A step of cold rolling the hot rolled steel sheet after winding to produce a cold rolled steel sheet;
The cold rolled steel sheet is heated at an average heating rate of 20 to 70 ° C./s in a temperature range of 300 to 650 ° C., and recrystallized and annealed at 800 to 950 ° C.
Cooling the cold-rolled steel sheet after the recrystallization annealing at a temperature range of 800 to 400 ° C. at an average cooling rate of 5 ° C./s or more;
Having a microstructure containing a ferrite phase of 50% or more in area ratio and a martensite phase of 1 to 15% in area ratio, and δ defined by the following formulas (2) and (3) is 0.3 The manufacturing method of the following high strength cold-rolled steel sheet;
[C]-(12 × [Nb] / 93) ≧ 0.01 (1)
δ = (σc / ρ) / TS (2)
σc = {E / (1-ν 2 )} × t × (1 / D 0 -1 / D 1 ) (3)
Here, [M] is the content of element M (% by mass) , E is the Young's modulus (MPa) of the steel, ν is the Poisson's ratio of the steel, t is the plate thickness (mm) of the steel plate, TS is the steel plate Represents tensile strength (MPa), D 0 is the outer diameter of the cup after cup molding the steel sheet with a draw ratio ρ (mm), D 1 cut out a ring sample from the side of the cup, rolling the steel sheet It represents the outer diameter (mm) of the ring perpendicular to the rolling direction when the ring sample is opened with a cut in the direction .
さらに、質量%で、Mo、Cr、CuおよびNiのうちから選ばれた少なくとも1種の元素を合計で0.5%以下含有する鋼スラブを用いる請求項1に記載の高強度冷延鋼板の製造方法。 2. The method for producing a high-strength cold-rolled steel sheet according to claim 1 , wherein the steel slab contains, in mass%, at least one element selected from Mo, Cr, Cu and Ni in total of 0.5% or less. . さらに、質量%で、Ti: 0.1%以下含有し、かつ下記の式(4)、および式(5)または式(6)を満たす鋼スラブを用いる請求項1または2に記載の高強度冷延鋼板の製造方法;
([Ti]/48)/([S]/32+[N]/14)≦2.0 ・・・(4)
Ti>0で、[C]-12×([Nb]/93+[ Ti]/48)≧0.01 ・・・(5)
Ti≦0で、[C]-12×[Nb]/93≧0.01 ・・・(6)
ここで、Ti=[Ti]-48×([N]/14+[S]/32)で、[M]は元素Mの含有量(質量%)を表す。
Further, high strength cold rolling according to claim 1 or 2 using a steel slab containing, by mass%, Ti: 0.1% or less and satisfying the following formula (4) and formula (5) or formula (6): Steel sheet manufacturing method;
([Ti] / 48) / ([S] / 32 + [N] / 14) ≦ 2.0 (4)
Ti * > 0, [C] -12 × ([Nb] / 93 + [Ti * ] / 48) ≧ 0.01 (5)
Ti * ≦ 0, [C] -12 × [Nb] /93≧0.01 (6)
Here, Ti * = [Ti] −48 × ([N] / 14 + [S] / 32), and [M] represents the content (mass%) of the element M.
前記再結晶焼鈍後の冷延鋼板を冷却する工程の後に、さらに前記冷延鋼板の表面にめっき層を形成する工程を有する請求項1から3のいずれか1項に記載の高強度冷延鋼板の製造方法。 The high-strength cold-rolled steel sheet according to any one of claims 1 to 3 , further comprising a step of forming a plating layer on a surface of the cold-rolled steel sheet after the step of cooling the cold-rolled steel sheet after the recrystallization annealing. Manufacturing method. 前記再結晶焼鈍後の冷延鋼板を冷却する工程に代え、前記再結晶焼鈍後の冷延鋼板を、800℃からめっき浴浸漬直前までの温度域を平均冷却速度5℃/s以上で冷却し、合金化後、合金化温度から400℃までの温度域を平均冷却速度5℃/s以上で冷却する工程を有する請求項1から4のいずれか1項に記載の高強度冷延鋼板の製造方法。 Instead of the step of cooling the cold-rolled steel sheet after the recrystallization annealing, the cold-rolled steel sheet after the recrystallization annealing is cooled at an average cooling rate of 5 ° C./s or more in a temperature range from 800 ° C. to immediately before immersion in the plating bath. The manufacturing of the high-strength cold-rolled steel sheet according to any one of claims 1 to 4 , further comprising a step of cooling a temperature range from the alloying temperature to 400 ° C after the alloying at an average cooling rate of 5 ° C / s or more. Method.
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