JPH02205657A - Manufacture of cold rolled steel sheet for ultradeep drawing - Google Patents
Manufacture of cold rolled steel sheet for ultradeep drawingInfo
- Publication number
- JPH02205657A JPH02205657A JP2508889A JP2508889A JPH02205657A JP H02205657 A JPH02205657 A JP H02205657A JP 2508889 A JP2508889 A JP 2508889A JP 2508889 A JP2508889 A JP 2508889A JP H02205657 A JPH02205657 A JP H02205657A
- Authority
- JP
- Japan
- Prior art keywords
- rolling
- less
- weight
- cold
- steel
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000010960 cold rolled steel Substances 0.000 title claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- 238000005096 rolling process Methods 0.000 claims abstract description 52
- 238000005097 cold rolling Methods 0.000 claims abstract description 36
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 24
- 239000010959 steel Substances 0.000 claims abstract description 24
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 7
- 239000007787 solid Substances 0.000 claims abstract description 3
- 239000012535 impurity Substances 0.000 claims abstract 3
- 238000005245 sintering Methods 0.000 claims description 6
- 238000004804 winding Methods 0.000 claims description 4
- 238000005554 pickling Methods 0.000 claims description 3
- 238000005098 hot rolling Methods 0.000 abstract description 20
- 238000000034 method Methods 0.000 abstract description 9
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 4
- 229910052698 phosphorus Inorganic materials 0.000 abstract description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 239000006104 solid solution Substances 0.000 description 11
- 238000005336 cracking Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 238000001953 recrystallisation Methods 0.000 description 7
- 229910000859 α-Fe Inorganic materials 0.000 description 5
- 238000000137 annealing Methods 0.000 description 4
- 238000005461 lubrication Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000004767 nitrides Chemical class 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910001566 austenite Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002436 steel type Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Heat Treatment Of Sheet Steel (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、深絞り性に極めて優れた冷延鋼板の製造方法
に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for manufacturing a cold rolled steel sheet having extremely excellent deep drawability.
従来、冷延綱板の製造工程においては、A、変態点以上
の仕上温度で熱間圧延した素材を酸洗し、75%程度の
冷延率で冷間圧延した後、焼純するのが一般的である。Conventionally, in the manufacturing process of cold-rolled steel sheets, A. A material that has been hot-rolled at a finishing temperature above the transformation point is pickled, cold-rolled at a cold rolling rate of about 75%, and then sintered. Common.
このような従来方法において、上記冷延鋼板のランクフ
ォード(!!(以下r値と記す)を向上させるためには
、上記冷延率を75%程度から90%程度に上げてやれ
ばよいことがわかっているが、この場合、冷延機の能力
の都合からこのような高圧下の冷延率を採用することは
困難であった。また、仮にレバース圧延機などを採用す
ることにより上記高冷延率での圧延が可能となったとし
ても、現実には熱延仕上板厚が酸洗ライン通過可能な最
大厚さ6鴎程度に制限されるので、これから例えばQ、
Elmtの冷延鋼板を製造する場合、87%の冷延率し
か取れず、結局上記高冷低率は実現困難であり、十分な
冷延集合組織の発達が望めない、その結果、再結晶焼純
後に深絞り性に有効な集合組織が発達せず、r値が2.
0前後となっていた。In such a conventional method, in order to improve the Lankford (!! (hereinafter referred to as r value)) of the cold-rolled steel sheet, it is sufficient to increase the cold rolling rate from about 75% to about 90%. However, in this case, it was difficult to adopt such a high cold rolling rate due to the capacity of the cold rolling mill.Also, if a reverse rolling mill etc. were adopted, the above-mentioned high rolling rate could be achieved. Even if rolling at a cold rolling rate becomes possible, in reality, the finished hot-rolled plate thickness is limited to the maximum thickness that can pass through the pickling line, so from now on, for example,
When producing Elmt cold-rolled steel sheets, only a cold-rolling rate of 87% can be obtained, and the above-mentioned high cold-rolling rate is difficult to achieve, and sufficient cold-rolling texture cannot be expected to develop.As a result, recrystallization and sintering After purification, no effective texture for deep drawability was developed, and the r value was 2.
It was around 0.
以上のように、従来の冷延鋼板の製造方法では、理想的
な冷延率が取れずに十分な冷延集合組織が得られないた
め、得られる深絞り性、つまりr値に限度があるという
問題点があった。As mentioned above, in the conventional manufacturing method of cold-rolled steel sheets, the ideal cold-rolling ratio cannot be obtained and a sufficient cold-rolled texture cannot be obtained, so there is a limit to the deep drawability that can be obtained, that is, the r value. There was a problem.
本発明の目的は、上記従来の状況に鑑みてなされたもの
で、深絞り性の極めて良好な冷延鋼板の製造方法を提供
することにある。The object of the present invention was made in view of the above-mentioned conventional situation, and it is an object of the present invention to provide a method for manufacturing a cold-rolled steel sheet having extremely good deep drawability.
本件発明者は、上記従来の問題点を解決するために鋭意
研究し、冷間圧延の集合組織の一部を熱延段階で作り、
続く冷間圧延でそれを完全なものとし、又冷延鋼板に要
求される形状、精度、表面品質については冷延段階で作
り上げればよいことを見出した。モして熱延段階で圧延
集合組織を形成するための条件は、フェライト域でかつ
未再結晶粒が得られることである点に想到して本発明を
成したものである。In order to solve the above-mentioned conventional problems, the inventor of the present invention conducted intensive research, created part of the texture of cold rolling at the hot rolling stage,
We perfected it through subsequent cold rolling, and also discovered that the shape, precision, and surface quality required for cold-rolled steel sheets could be achieved during the cold-rolling stage. The present invention was developed based on the idea that the conditions for forming a rolling texture in the hot rolling stage are that unrecrystallized grains are obtained in the ferrite region.
そこで本願第1項の発明は、C: 0.01重量%以下
、Si :0.1重量%以下、Mn:0.3重量%以
下、P:0.02重量%以下、S : 0.015重量
%以下、N : 0.01重量%以下を含存し、Nb:
0.2重!94以下で、かつ(C/12) < (0,
6×Nb /93)となる量のNbを添加した綱に対し
、900℃〜1200℃で粗圧延を施すとともに、Nb
の炭化物を析出させて固溶Cを20ppm以下とし、6
50℃以上で仕上板厚1.に対してロール径D1がDt
>100 tlとなる圧延ロールを用いてT (’C
) −880−5500X(C%)以下での圧下率R1
の仕上圧延を行い、600℃以下で巻取り、酸洗後、仕
上板厚t8に対してロール径D8がDt >100 t
、となる圧延ロールを用いて圧下率Rz>50%(但し
、R。Therefore, the invention of item 1 of the present application provides C: 0.01% by weight or less, Si: 0.1% by weight or less, Mn: 0.3% by weight or less, P: 0.02% by weight or less, S: 0.015. % by weight or less, Nb: 0.01% by weight or less, Nb:
0.2 layers! 94 or less, and (C/12) < (0,
6×Nb/93) is subjected to rough rolling at 900°C to 1200°C, and the Nb
carbide is precipitated to reduce the solid solute C to 20 ppm or less, and 6
Finished plate thickness at 50℃ or higher 1. The roll diameter D1 is Dt
T ('C
) -880-5500X (C%) or less rolling reduction R1
After finish rolling, winding at 600°C or less, and pickling, the roll diameter D8 is Dt > 100 t with respect to the finished plate thickness t8.
, using a rolling roll with a rolling reduction ratio Rz>50% (however, R.
とR2との合計圧下率Rは95%>R>75%)の冷間
圧延を施した後、焼純するようにした製造方法である。This is a manufacturing method in which cold rolling is performed such that the total reduction ratio R of R2 and R2 is 95%>R>75%) and then sintered.
また、本願第2項の発明は、上記第1項の発明における
化学成分の鋼にB : 0.0005〜0.005重量
%を含有させ、これを上記製造方法に通用したものであ
る。なお、ここで合計圧下率Rは下記式で求められる。Further, the invention of item 2 of the present application is such that the steel having the chemical composition in the invention of item 1 above contains B: 0.0005 to 0.005% by weight, and this is applicable to the above manufacturing method. In addition, the total rolling reduction ratio R is calculated|required here by the following formula.
R−1−(1−R+ )x (1−Rg )また、粗圧
延については従来の再加熱圧延でも、鋳造後ただちに圧
延を行う直接圧延であっても良い。R-1-(1-R+)x (1-Rg) Furthermore, the rough rolling may be conventional reheat rolling or direct rolling in which rolling is performed immediately after casting.
ここで本願発明の成分限定理由及び製造条件について説
明する。Here, the reason for limiting the components and manufacturing conditions of the present invention will be explained.
まず特定発明における成分限定理由について説明する。First, the reason for limiting the components in the specific invention will be explained.
C,Nは、それぞれ0.01%を越えて添加すると、N
bC,TiN、AjNなどの析出物が多くなるため製品
の加工性が悪(なり、又これを固着するためのNb、A
jの量が多くなって高価になることから、−C1,01
%、N≦0.01%とした。When C and N are added in excess of 0.01% each, N
The processability of the product is poor due to the increase in precipitates such as bC, TiN, and AjN.
Since the amount of j increases and becomes expensive, -C1,01
%, N≦0.01%.
S i、 Mn、 Pはそれぞれ固溶強化元素として作
用し、r値や伸びを低下させ、本発明の目的である超深
絞り性が達成できないため、それぞれの上限値以下に規
制しなければならない、Sは伸長した介在物の原因とな
り局部延性を低下させるため0゜015%以下にしなけ
ればならない。Si, Mn, and P each act as solid solution strengthening elements and reduce the r value and elongation, making it impossible to achieve the ultra-deep drawability that is the objective of the present invention, so they must be regulated below their respective upper limit values. , S cause elongated inclusions and reduce local ductility, so they must be kept at 0°015% or less.
Nbは、これを添加することで、その炭、窒化物を形成
させて鋼中の固溶Cを減じ、さらにフェライト再結晶温
度を大幅に上げることができ、加工中の回復も遅らせる
ことが可能になる。これによって冶金的にみた場合、冷
間で圧延したのと同様な状態を高温域まで延長すること
ができ、冷間集合組織の一部分を熱間圧延時に作ること
が可能となる。この効果は同量のTiや■では達成でき
ずNb特有の現象である。そしてこのNbの添加量は炭
、窒化物を形成して鋼中の固溶Cを固定するに必要な量
、即ち(C/12) <(0,6×Nb /93)を満
足する量とし、かつ経済性をも考慮してNb1.2重量
%以下とした。By adding Nb, it is possible to form carbon and nitrides to reduce solid solution C in steel, and also to significantly increase the ferrite recrystallization temperature, which also delays recovery during processing. become. As a result, from a metallurgical point of view, it is possible to extend the state similar to cold rolling to a high temperature range, and it is possible to create a part of the cold texture during hot rolling. This effect cannot be achieved with the same amount of Ti or ■, and is a phenomenon unique to Nb. The amount of Nb added is the amount necessary to form carbon and nitrides and fix the solid solution C in the steel, that is, the amount that satisfies (C/12) < (0,6 x Nb /93). , and considering economic efficiency, the Nb content was set to 1.2% by weight or less.
Bは、これを添加することで耐たて割れ性を改善できる
。即ち、Nbを添加することにより、固溶Cを低減する
ことができるが、この固溶Cの低減は結晶粒界の結合力
を弱め、2次加工時の耐たて割れ性を劣化させる。そこ
でBを添加することで、このBを結晶粒界に偏析させて
結晶粒界の結合力を強めることができる。ここで、Bの
添加量についてはo、ooos%未満では上述の効果が
得られず、0.005%を越える添加は経済的に不利な
上、過剰なりの添加は製品の深絞り性に悪影響を及ぼす
ことから、o、 ooos%〜o、oos%とした。By adding B, the warp cracking resistance can be improved. That is, by adding Nb, solid solution C can be reduced, but this reduction in solid solution C weakens the bonding force of grain boundaries and deteriorates the warp cracking resistance during secondary processing. Therefore, by adding B, it is possible to segregate this B at the grain boundaries and strengthen the bonding force at the grain boundaries. Here, regarding the amount of B added, if it is less than o or oos%, the above effect cannot be obtained, and if it is added in excess of 0.005%, it is economically disadvantageous, and if it is added in excess, it will have a negative effect on the deep drawability of the product. Therefore, it was set as o,oos% to o,oos%.
次に製造条件について説明する。Next, manufacturing conditions will be explained.
Nbの炭化物析出処理を行う点:固溶Cが20pp麟以
上含まれている状態で未再結晶フェライト域圧延を施し
ても、再結晶焼純時に板面に平行な(111)集合組織
は発達せず、深絞り性に悪影響を及ぼす(200)集合
組織が発達する。冷間圧延で高い深絞り性を得ようとす
る場合には、熱間圧延終了後に高温で巻取って炭、窒化
物を析出させておくことが必要であるが、これと同様に
650℃以上の温度範囲での、未再結晶圧延前に、Nb
の炭化物を析出させて、鋼中の固溶Cを減じておくこと
が必要である。The point of performing Nb carbide precipitation treatment: Even if rolling is performed in the non-recrystallized ferrite region in a state where solid solution C is included at least 20 ppm, the (111) texture parallel to the sheet surface will develop during recrystallization annealing. (200) texture develops, which adversely affects deep drawability. In order to obtain high deep drawability through cold rolling, it is necessary to coil at a high temperature after hot rolling to precipitate carbon and nitrides. Nb before unrecrystallized rolling at a temperature range of
It is necessary to precipitate carbides to reduce solid solution C in the steel.
ここで熱延仕上前に、NbCを充分に析出させる方法と
しては次の3つが考えられる。Here, the following three methods can be considered for sufficiently precipitating NbC before hot rolling finishing.
■ 再加熱圧延の場合、スラブ加熱温度を900℃〜1
100℃と低温にして、スラブ加熱段階で析出物をあま
り固溶させない方法。■ For reheat rolling, increase the slab heating temperature to 900℃~1
A method that uses a low temperature of 100°C to prevent precipitates from forming a solid solution during the slab heating stage.
、■ 粗圧延温度を900〜1000℃と低くして、T
I。, ■ The rough rolling temperature is lowered to 900 to 1000°C, and T
I.
Nbの炭化物を圧延誘起析出させる方法。A method for rolling-induced precipitation of Nb carbide.
■ 粗圧延の終了から熱延仕上までに時間をおいて、こ
の間に炭化物を析出させる方法(この場合、待ち時間は
析出物生成温度域で4分以上が望ましい)。(2) A method in which a period of time is allowed between the end of rough rolling and the finishing of hot rolling, and carbide is precipitated during this period (in this case, the waiting time is preferably 4 minutes or more in the precipitate formation temperature range).
熱間圧延温度を650℃以上とした点、及びT(t)
−880−5500x (C%)以下での熱延と冷間圧
延との合計圧下率を75%以上95%以下とした点:
T (℃) −880−5500x (C%)を越える
温度での圧延では、フェライト+オーステナイトあるい
はオーステナイト域となり、圧延集合組織が残らない、
T (℃) −880−5500x (C%)と65
0℃の間の熱延は未再結晶フェライト域での圧下であり
、その圧下率が次工程の冷間圧延とともに圧延集合&[
l織を形成する上で重要であり、従ってトータルで75
〜95%になるようこの温度域での圧下量を制御する。The hot rolling temperature is 650°C or higher, and T(t)
-880-5500x (C%) The total reduction ratio of hot rolling and cold rolling is 75% or more and 95% or less:
When rolling at temperatures exceeding T (℃) -880-5500x (C%), the result is ferrite + austenite or an austenite region, and no rolling texture remains.
T (℃) -880-5500x (C%) and 65
Hot rolling at 0°C is rolling in the unrecrystallized ferrite region, and the rolling reduction rate is the rolling set & [
It is important in forming the l weave, so a total of 75
The amount of pressure reduction in this temperature range is controlled to 95%.
一方、650℃未満の温度での圧延では材料の変形抵抗
が大きすぎるので、実際的ではない。On the other hand, rolling at a temperature below 650° C. is not practical because the deformation resistance of the material is too high.
また、再結晶焼純で深絞り性に有効な集合組織を得るた
めには、冷延集合組織を十分に発達させておかなければ
ならない、そのためには、先のフェライト未再結晶域で
の圧延率と冷間圧延率との合計が75〜95%必要であ
る。即ち、熱間圧延での圧下率R1は、それに続く冷間
圧延の圧下率R□との合計圧下率R(=1 (l
R+)X(1−R2)〕が75%以上95%以下とな
るようにする。In addition, in order to obtain a texture that is effective for deep drawability in recrystallization annealing, the cold rolling texture must be sufficiently developed. The sum of the rolling rate and the cold rolling rate is required to be 75 to 95%. That is, the rolling reduction ratio R1 in hot rolling is the total rolling reduction ratio R(=1 (l
R+)X(1-R2)] is 75% or more and 95% or less.
また巻取り温度は巻取り段階で再結晶しない条件、つま
り600℃以下にする必要がある。それ以上になると冷
延との積算効果が期待で、きなくなるからである。Further, the winding temperature must be kept under conditions that do not cause recrystallization during the winding stage, that is, 600° C. or lower. This is because if it exceeds the expected cumulative effect of cold rolling, it will no longer be possible.
この場合、冷間圧延については、上記熱間圧延で作られ
た集合組織を完全なものとし、かつ表面形状を整えるた
めに、50%以上の圧下率を必要とする。In this case, the cold rolling requires a reduction ratio of 50% or more in order to perfect the texture created by the hot rolling and to adjust the surface shape.
熱間圧延における潤滑:熱延時の潤滑については、この
潤滑が優れている程冷延と同等の特性がもたらされ好ま
しいが、潤滑条件が悪くとも冷延との合計圧下率が本発
明範囲であれば、それ以下の圧下率の冷延鋼板よりも高
いr値を得ることができるので、特に規定する必要はな
い。Lubrication during hot rolling: Regarding lubrication during hot rolling, the better the lubrication, the better the properties equivalent to those of cold rolling, but even if the lubrication conditions are poor, as long as the total reduction with cold rolling is within the range of the present invention. Since it is possible to obtain a higher r value than a cold-rolled steel sheet with a rolling reduction of less than , there is no need to specify it in particular.
ロール径を規定した点:ロール径が仕上板厚に比べてあ
まり小さいと、冷延率を高くしても板の中心部まで板圧
方向の歪が入らず、十分な冷延集合組織が得られない、
そのため、仕上板厚tに対してロール径りをD>100
’tとなるようにする。The point of specifying the roll diameter: If the roll diameter is too small compared to the finished sheet thickness, even if the cold rolling rate is increased, strain in the sheet pressure direction will not reach the center of the sheet, and a sufficient cold rolling texture will not be obtained. I can't do it,
Therefore, the roll diameter should be D>100 for the finished plate thickness t.
't.
なお、このことは冷延ロールについても同様である。Note that this also applies to cold rolling rolls.
本発明に係る冷延鋼板の製造方法においては、Nbの炭
化物を析出させて鋼中の固溶Cを低減するとともに、所
定ロール径の圧延ロールによって所定温度範囲、圧下率
の熱間圧延及び冷間圧延を行うようにしたので、冶金的
に見て冷間のみで圧延したのと略同様な状態を、高温域
まで延長することができ、深絞り性に影響する冷延集合
組織をこの両圧延で発達させることが可能となり、高い
深絞り性が得られる。In the method for manufacturing a cold rolled steel sheet according to the present invention, solid solution C in the steel is reduced by precipitating Nb carbides, and hot rolling and cold rolling are performed at a predetermined temperature range and reduction rate using rolling rolls having a predetermined roll diameter. By performing inter-rolling, it is possible to extend the state that is almost the same as that obtained by cold rolling from a metallurgical point of view to a high temperature range, and the cold-rolling texture, which affects deep drawability, can be improved by both cold-rolling textures. It can be developed by rolling, resulting in high deep drawability.
従って上記条件を満たす熱間圧延が行われるならば仕上
げ熱延の入り側温度がT (t) −880−5500
X (C%)を越えても差しつかえない。Therefore, if hot rolling is performed that satisfies the above conditions, the temperature at the entry side of finishing hot rolling is T (t) -880-5500
There is no problem even if it exceeds X (C%).
また、本願の関連発明においては、Bを添加するように
したことから、上述の効果に加えて鋼中の固溶Cの低減
に起因する耐たて割れ性の劣化が防止できる。Furthermore, in the related invention of the present application, since B is added, in addition to the above-mentioned effects, it is possible to prevent deterioration of warp cracking resistance due to a reduction in solid solution C in the steel.
以下、本発明の実施例を図について説明する。 Hereinafter, embodiments of the present invention will be described with reference to the drawings.
まず、本願第1項の発明の実施例について説明する。First, an embodiment of the invention of item 1 of the present application will be described.
第1表は本発明の鋼(表中、C,D)及び比較鋼(表中
、A、 B)の化学成分を示す。Table 1 shows the chemical composition of the steel of the present invention (C, D in the table) and the comparative steel (A, B in the table).
本実施例では第1表に示す4鋼種を転炉で溶製し、通常
の工程でスラブを製造した後、第2表に示す条件で熱間
圧延を行い、これをコイルに巻取り、酸洗した後、これ
も第2表に示す条件で冷間圧延を行い、850℃×1.
5分の連続焼純(CAL)もしくは750℃×3時間の
バッチ焼純(BOX)を行い、材料のr値を測定した。In this example, the four steel types shown in Table 1 were melted in a converter, a slab was manufactured using the normal process, and then hot rolled under the conditions shown in Table 2, wound into a coil, and After washing, this was also cold rolled under the conditions shown in Table 2 at 850°C x 1.
Continuous sintering (CAL) for 5 minutes or batch sintering (BOX) at 750°C for 3 hours was performed to measure the r value of the material.
その結果を第2表に示す。The results are shown in Table 2.
第2表からも明らかなように、本願発明の鋼(第3.4
.6,7.10欄)では、いずれにおいてもr値が2.
0以上と高く、良好な深絞り性が得られていることがわ
かる。As is clear from Table 2, the steel of the present invention (Section 3.4)
.. 6, 7.10), the r value is 2.
It can be seen that good deep drawability is obtained, which is as high as 0 or more.
また本件発明者は、圧延率と深絞り性(r値)との関係
について実験を行った。The inventor also conducted an experiment regarding the relationship between rolling reduction and deep drawability (r value).
図は、上記実験結果を示す特性図である。この実験は、
0.0025%C−0,02%Si −0,15%Mn
−0,001%S−0,025%Nb−0,003%
Nの熱延板を、圧下率を変化させて冷間圧延し、850
℃×2分の再結晶焼純した後、r値を測定した(図中、
・印で示す)、また、上記鋼を全圧下率の半分を860
℃以下の熱延で行い、残り半分を冷延で行って、同様に
850℃×2分の再結晶焼純をした後、r値を測定した
(図中、○印で示す)。The figure is a characteristic diagram showing the above experimental results. This experiment
0.0025%C-0,02%Si-0,15%Mn
-0,001%S-0,025%Nb-0,003%
A hot-rolled plate of N was cold-rolled by varying the rolling reduction ratio, and
After recrystallization and annealing for 2 minutes at °C, the r value was measured (in the figure,
・Indicated by mark), and half of the total rolling reduction of the above steel is 860
℃ or less, the remaining half was cold rolled, and after recrystallization and annealing at 850° C. for 2 minutes, the r value was measured (indicated by a circle in the figure).
同図からも明らかなように、合計圧下率75〜95%の
範囲では、いずれも(○、・印)2.0以上のr値が得
られていることがわかる。As is clear from the figure, in the range of the total rolling reduction of 75% to 95%, r values of 2.0 or more are obtained in all cases (marked with ◯ and *).
次に、本願第2項の発明の実施例について説明する。Next, an embodiment of the invention of Section 2 of the present application will be described.
第3表は本発明の綱(表中のE、F)の化学成分を示す
0本実施例では第3表に示す2fl4種を溶製し、通常
の工程でスラブを製造した後、1100℃に再加熱して
T域で30fi厚さに粗圧延し、2分間経過後920℃
になったところで仕上圧延を行い、855℃以下の圧下
率を60%にして2.9flの厚さに仕上げ、仕上温度
は画調(E、 C)とも770℃程度とした0次に、こ
れを500℃で巻取った後、酸洗して冷間圧延した。こ
の冷間圧延の仕上板厚は0.8 fiであるから、85
5℃以下の温度範囲での圧下率は合針89%である。ま
た熱間圧延のロール径はφ800、冷間圧延のロール径
はφ580である。Table 3 shows the chemical composition of the steel of the present invention (E, F in the table). Reheated and roughly rolled to 30fi thickness in T area, 920℃ after 2 minutes.
Finish rolling was carried out at a temperature of 60% below 855°C to a thickness of 2.9 fl, and the finishing temperature was approximately 770°C for both image scales (E and C). After being wound up at 500°C, it was pickled and cold rolled. The finished plate thickness of this cold rolling is 0.8 fi, so 85
The rolling reduction ratio in a temperature range of 5° C. or less is 89%. Further, the roll diameter for hot rolling is φ800, and the roll diameter for cold rolling is φ580.
そして、上記製造方法により得られた鋼板を850℃×
1.5分の連続焼純した後、r値の測定及び2次加工時
の耐たて割れ性の試験を行った。この耐たて割れ性の試
験はカップ縦割れ試験を採用し、鋼板をφ145でブラ
ンクした後、絞り比α:2.0で試験用カップを作製し
、これを液体窒素温度から常温までの温度範囲で、円錐
ポンチにかぶせてカップ底面から荷重をかけて破壊し、
その時の脆性破壊率から遷移温度を測定した。Then, the steel plate obtained by the above manufacturing method was heated to 850°C
After continuous sintering for 1.5 minutes, the r value was measured and the warp cracking resistance test during secondary processing was conducted. This vertical cracking resistance test adopted a cup vertical cracking test, in which a steel plate was blanked with a diameter of 145 mm, a test cup was prepared with a drawing ratio of α: 2.0, and the cup was heated at temperatures ranging from liquid nitrogen temperature to room temperature. Place it over a conical punch and apply a load from the bottom of the cup to destroy it.
The transition temperature was measured from the brittle fracture rate at that time.
その実験結果を第4表に示す。The experimental results are shown in Table 4.
同表によれば、111EではCが残存しているため、!
[FではBを添加することによって脆性遷移温度が低下
し、両者とも良好な耐たて割れ性を示していることがわ
かる。According to the same table, C remains in 111E, so!
[It can be seen that in F, the brittle transition temperature is lowered by adding B, and both exhibit good warp cracking resistance.
以上のように、本願第1.第2項の発明に係る超深絞り
用冷延鋼板の製造方法によれば、Nbの炭化物を析出さ
せて鋼中の固溶Cを低減するとともに、熱延段階で冷間
圧延集合組織の一部又はそのほとんどを作り、冷延段階
でこの集合m織を完全なものとするとともに表面性状を
整えるようにしたので、表面性状に優れ、かつ深絞り性
に極めて優れた冷延鋼板が得られる効果がある。As mentioned above, this application No. 1. According to the method for producing a cold-rolled steel sheet for ultra-deep drawing according to the invention of item 2, Nb carbide is precipitated to reduce solid solution C in the steel, and the cold-rolling texture is improved during the hot-rolling stage. By completing the aggregated weave and adjusting the surface texture during the cold rolling stage, a cold-rolled steel sheet with excellent surface texture and extremely excellent deep drawability can be obtained. effective.
また本願第2項の発明によれば、さらにBを添加するよ
うにしたので、Cの原子当量以上にNbを添加した鋼に
おいて、上記効果に加えて耐たて割れ性を確保できる効
果がある。Furthermore, according to the invention in item 2 of the present application, since B is further added, in addition to the above-mentioned effects, it is possible to ensure warp cracking resistance in steel in which Nb is added in an amount greater than the atomic equivalent of C. .
図面は本発明の詳細な説明するための圧下率とr値との
関係を示す特性図である。The drawing is a characteristic diagram showing the relationship between rolling reduction and r value for explaining the present invention in detail.
Claims (2)
下、Mn:0.3重量%以下、P:0.02重量%以下
、S:0.015重量%以下、N:0.01重量%以下
を含有し、Nb:0.2重量%以下で、かつ(C/12
)く(0.6×Nb/93)となるような量のNbを添
加した残部Fe及び不可避的不純物よりなる鋼に対し、
900℃〜1200℃の温度範囲にて粗圧延を施すとと
もに、Nbの炭化物を析出させて鋼中の固溶C総量を2
0ppm以下とし、650℃以上の温度範囲で、仕上板
厚t_1に対してロール径D_1がD_1>100t_
1となる圧延ロールを用いてT(℃)=880−550
0×(C%)以下での圧下率R_1の仕上圧延を施した
後600℃以下で巻取り、酸洗を行い、さらに仕上板厚
t_2に対してロール径D_2がD_2>100t_2
となる圧延ロールを用いて圧下率R_2>50%(但し
、R_1とR_2の合計圧下率Rは95%>R>75%
)の冷間圧延を施した後、焼純を行うようにしたことを
特徴とする超深絞り用冷延鋼板の製造方法。(1) C: 0.01% by weight or less, Si: 0.1% by weight or less, Mn: 0.3% by weight or less, P: 0.02% by weight or less, S: 0.015% by weight or less, N: Contains 0.01% by weight or less, Nb: 0.2% by weight or less, and (C/12
) (0.6×Nb/93) for steel with the balance Fe and unavoidable impurities,
Rough rolling is performed at a temperature range of 900°C to 1200°C, and Nb carbide is precipitated to reduce the total amount of solute C in the steel to 2.
0 ppm or less, and in a temperature range of 650°C or higher, the roll diameter D_1 is D_1>100t_ with respect to the finished plate thickness t_1.
T (°C) = 880-550 using a rolling roll of 1
After finish rolling with a rolling reduction R_1 at 0x(C%) or less, it is rolled up at 600°C or less, pickled, and further the roll diameter D_2 is D_2>100t_2 with respect to the finished plate thickness t_2.
Using a rolling roll, the rolling reduction ratio R_2>50% (however, the total rolling reduction ratio R of R_1 and R_2 is 95%>R>75%
) A method for producing a cold-rolled steel sheet for ultra-deep drawing, characterized in that after cold rolling, sintering is performed.
下、Mn:0.3重量%以下、P:0.02重量%以下
、S:0.015重量%以下、N:0.01重量%以下
、B:0.0005〜0.005重量%を含有し、Nb
:0.2重量%以下で、かつ(C/12)<(0.6×
Nb/93)となるような量のNbを添加した残部Fe
及び不可避的不純物よりなる鋼に対し、900℃〜12
00℃の温度範囲にて粗圧延を施すとともに、Nbの炭
化物を析出させて鋼中の固溶c総量を20ppm以下と
し、650℃以上の温度範囲で、仕上板厚t_1に対し
てロール径D_1がD_1>100t_1となる圧延ロ
ールを用いてT(℃)−880−5500×(C%)以
下での圧下率R_1の仕上げ圧延を施した後、600℃
以下で巻取り、酸洗いを行い、さらに仕上板厚t_2に
対してロール径D_2がD_2>100t_2となる圧
延ロールを用いて圧下率R_2>50%(但し、R_1
とR_2の合計圧下率Rは95%>R>75%)の冷間
圧延を施した後、焼純を行うようにしたことを特徴とす
る超深絞り用冷延鋼板の製造方法。(2) C: 0.01% by weight or less, Si: 0.1% by weight or less, Mn: 0.3% by weight or less, P: 0.02% by weight or less, S: 0.015% by weight or less, N: Contains 0.01% by weight or less, B: 0.0005 to 0.005% by weight, Nb
: 0.2% by weight or less, and (C/12)<(0.6×
Nb/93)
and unavoidable impurities, 900℃~12
Rough rolling is performed in a temperature range of 00°C, Nb carbide is precipitated, the total amount of solid solute c in the steel is 20 ppm or less, and roll diameter D_1 is applied to the finished plate thickness t_1 in a temperature range of 650°C or higher. After performing finish rolling at a reduction rate R_1 at T (°C) -880-5500 x (C%) or less using a rolling roll where D_1>100t_1, 600°C
Below, winding and pickling are performed, and further, rolling reduction ratio R_2>50% (however, R_1
and R_2 (total reduction ratio R of 95%>R>75%), and then sintering is performed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2508889A JPH02205657A (en) | 1989-02-02 | 1989-02-02 | Manufacture of cold rolled steel sheet for ultradeep drawing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2508889A JPH02205657A (en) | 1989-02-02 | 1989-02-02 | Manufacture of cold rolled steel sheet for ultradeep drawing |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02205657A true JPH02205657A (en) | 1990-08-15 |
Family
ID=12156167
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2508889A Pending JPH02205657A (en) | 1989-02-02 | 1989-02-02 | Manufacture of cold rolled steel sheet for ultradeep drawing |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02205657A (en) |
-
1989
- 1989-02-02 JP JP2508889A patent/JPH02205657A/en active Pending
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