JPH0159330B2 - - Google Patents
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- JPH0159330B2 JPH0159330B2 JP11839086A JP11839086A JPH0159330B2 JP H0159330 B2 JPH0159330 B2 JP H0159330B2 JP 11839086 A JP11839086 A JP 11839086A JP 11839086 A JP11839086 A JP 11839086A JP H0159330 B2 JPH0159330 B2 JP H0159330B2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/002—Heat treatment of ferrous alloys containing Cr
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Heat Treatment Of Sheet Steel (AREA)
Description
(産業上の利用分野)
本発明はCr系ステンレス鋼薄肉鋳片の製造方
法に関するものである。
(従来の技術)
ステンレス鋼薄鋼板は例えば特開昭55−97430
号公報に記載されている如く、板厚200mm前後に
連続鋳造された鋳片を粗圧延もしくは1200℃に加
熱後、熱間仕上圧延して熱延板とし、ベル型の焼
鈍炉により熱延板焼鈍を施こして、冷間圧延、仕
上焼鈍を行い、製品とされている。
(発明が解決しようとする問題点)
上記の如く、公知の技術は鋳片の厚みが厚く、
所定の熱延板にするための諸エネルギーを必要と
し、またかかる鋳片は熱延ままの状態でα′相が形
成されているので、これを分解して冷延性を向上
させるためにベル型の焼鈍炉により長時間の焼鈍
を必要としている。
(問題点を解決するための手段)
本発明は、Cr系ステンレス鋼の造塊において、
溶鋼を連続鋳造で薄肉鋳片とし、該鋳片をγ相の
析出終了する温度までをα相領域内にあるように
冷却することにより、γ相を析出せしめない状態
の鋳片を製造することを骨子とするものであり、
かかる鋳片を出発材料とすることにより所定の熱
延板にするための諸エネルギー、諸設備を必要と
せず、また、熱延板焼鈍相当工程を省略しても冷
延性及びリジング特性の良好な薄鋼板を製造する
ことができるという効果が奏せられる。
以下、本発明を詳細に説明する。
本発明の第1の目的は、Cr系ステンレス鋼薄
板の製造において、冷延性向上のために行つてい
る熱延板焼鈍に相当する工程の省略にある。
Cr系ステンレス鋼薄板の中でも、SUS410等に
代表される鋼種においては、熱延ままの状態で
は、γ相の変態により生成された硬い相が多量に
存在するため、このままの状態で冷間圧延する
と、冷延破断したり、冷間圧延時の圧下率が一定
にならず、コイル長手方向の厚みの変動が大きく
なる等の欠陥が生ずるため、熱延板焼鈍により、
この硬い相をフエライト+炭化物に分離するため
の熱延板焼鈍を行うことが必要である。
本発明者等はこの熱延板焼鈍工程を省略する方
策について研究した結果、硬い相の生成原因とな
るγ相を生成しないように凝固後、γ相の析出終
了温度まで、α相領域内にあるように冷却し、γ
相のない熱延板を作れば、硬い相が形成されない
ので、上述の熱延板焼鈍に相当する工程は不必要
になることを見い出したものである。即ち、厚さ
200mm前後の鋳片の場合は、鋳造後通常の方法で
鋳片表面を冷却しても、冷却速度は、鋳片自身の
熱伝導率によつて制約されて、凝固過程でγ相の
析出を防止することが出来ないが、鋳片厚みを所
定の厚みに制限し、凝固後α相領域内にあるよう
に冷却することにより、γ相を析出させないでα
相+炭化物の存在する領域にもち来たすことを可
能にしたものである。α相+炭化物の領域におい
て、α相中に過飽和に固溶したC、N、S等は、
炭窒化物や硫化物の形になるような析出処理が必
要である。このような析出処理を施さない場合
は、冷間圧延中での加工硬化が著しく、かつ最終
成品における伸びが小さく降伏点が高いという欠
点が生じる。
即ち、冷延性を向上させるため、γ相から形成
されたα′相をα+炭化物に分解するための熱延板
焼鈍に代えて過飽和αからC、N、S等を析出さ
せる析出処理のみの熱処理を行なえば冷延性が向
上し、また、この析出処理は、α′→α+炭化物の
反応に比し短時間でできかつ、通常の捲取り過程
で可能であり、特別の熱処理工程は不必要であ
る。
本発明の第2の目的は、加工性特にリジング特
性の改善された薄板を薄肉鋳片を出発材として製
造する技術を提供することにある。リジング特性
の改善のためには、コロニー(近似した方位を有
した結晶粒の集団)のサイズが小さく且つ、コロ
ニーがランダムに分散し、結晶粒径も比較的小さ
いことが必要である。このためには、鋳片の結晶
粒径を小さくし、かつ凝固後の冷却過程での粒界
移動に基づくロコニーサイズの増大を防止する必
要がある。
従来の鋳片は、100mm以上と、厚さが大きいの
で鋳造時の凝固速度の制御が困難であり、鋳造ま
まの状態で結晶粒径を小さくすることは不可能で
ある。
また、鋳造後の鋳片の冷却速度も、鋳片厚さが
大きく困難であることに起因して冷却中の高温域
での粒界移動に基づくコロニーサイズの増大等が
あり、熱間圧延工程で再結晶させてコロニーサイ
ズを小さくする必要がある。
しかし、本発明における如き薄肉鋳片では、鋳
片の厚さを10mm以下、好ましくは3mm以下と限定
することにより、鋳造後の凝固速度を速くできる
から、鋳片の結晶粒を小さくすることが可能であ
り、さらに凝固後の冷却速度を本発明の如く速く
採ることにより、コロニーサイズを小さくでき
る。高温でα+γ2相となる成分を有したSUS430
に代表されるCr系ステンレス鋼においては鋳造
ままの状態で、コロニーサイズの微細化ができな
い、通常の厚さの鋳片でコロニーサイズを微細化
させるにはγ相を微細分散させる必要がある。γ
相を微細分散させる技術としては、例えば鋳造さ
れた鋳片をα単相域に再熱後、大圧下を加えた後
α+γ2相域に冷却する技術(特開昭54−11827号
公報)や、熱延板をα+γ2相域に加熱する技術、
更に、粗圧延と仕上圧延間でα+γ2相域に加熱
する技術(特開昭59−83724号公報)等の先行技
術がある。α単相域に再加熱する方法の場合、高
温に再加熱され、α相の結晶粒が粗大化するた
め、最終目的とするリジング特性の改善効果が小
さい。熱延板をα+γ2相域に再加熱する方法は、
リジング特性向上効果は著しく大きいが、冷延性
が劣化し、且つきらきら疵等の表面欠陥が出やす
い。粗圧延と仕上圧延の間でα+γ2相域に加熱
する方法は、リジング特性の向上効果が大きく、
冷延性の劣化、きらきら疵等の表面欠陥の発生も
なく、以上3つの方策の中では最も優れた方式で
ある。
本発明者等は、これらの方策を改良発展させ
て、γ相の微細分散の方式を見い出したものであ
る。即ち凝固終了後、α相領域において鋳片を冷
却してγ相の析出を防止した後、α+γ相域に再
加熱してγ相の析出を行わせるものである。凝固
過程でγ相を析出させる場合と比べて、α相から
Cr炭化物等の析出物が微細析出した後にγ相が
析出するため、これらの析出物がγ析出のサイト
となることと、低温からγ相の析出がおきるの
で、γ相の成長速度が遅く、従つて高温からの冷
却過程でγ相を析出させる場合と比較して微細な
γ相を高密度に析出分散させることが可能とな
る。この場合、α+γ2相域に再加熱する以前に
加工を加えることでγ相の析出サイトが増すので
γ相の微細分散がより効果的に行われる。
本発明において、加工を加える他の目的は、急
冷凝固により生じたザクを圧着し冷延破断を防止
することおよび加工により高温での再結晶を促進
させることにある。
この場合、ザクの圧着のためには5%以上の圧
下を加えれば効果を発揮できるけれども、加工に
よる再結晶促進のためには25%以上、好ましく
は、35%以上の圧下を必要とする。
次に本発明の出発材の成分限定理由について説
明する。
Crを8%以上としたのは、これ未満のCr量で
は耐食性が劣るためである。Crの添加量が増す
程耐食性は向上するが30%を超えると効果が少な
く、且つ冷延性を劣化し、経済性を考慮するとこ
れ以上のCr量は好ましくないので30%を上限と
した。
Cを0.001%以上としたのは、これ未満のC量
の出発材を溶製することは、通常の方法では困難
なので、0.001%以上とした。Cは添加量が多い
程リジング特性が良くなるが、0.5%を超えて添
加すると冷延性やr値が劣化するので上限を0.5
%とした。
Alは添加量が多い程r値が向上するが、0.5%
を超えて添加しても効果は飽和し、経済的でない
ので上限を0.5%としたもので、下限を0.001%と
したのは、これ未満のAl量ではO2が著しく増し、
好ましくないので下限を0.001%としたものであ
る。
Nは添加量が多い程リジング特性が向上する
が、0.5%を超えて添加するとブリスター等が発
生するので上限を0.5%としたものであり、Nは
0.004%以下低い程r値が向上して好ましいが、
0.001%未満は通常の方式では溶製出来ないので
0.001%を下限としたものである。
本発明における出発材の成分は、Crが8〜30
%の範囲で、常温でα+(炭化物)となるような
成分であればどのような元素が入つていても本発
明の対象に入るものであり、すべての温度域でα
単相となるような成分組成の場合も、鋳片を急冷
することにより粒成長を防止することができる
が、この場合、C、N、S等が過飽和に固溶して
鋳片が異常に硬化するので、これら過飽和O、
N、Sを析出させることにより、粒径が小さく延
性のある鋳片の製造が可能であり、本発明の範囲
に包含されるものであるが、本発明の主たる目的
を達成する成分としては、高温でα、γ2相とな
るような成分系であることは言うまでもない。
本発明の出発材における鋳片厚みは、1mm以上
30mm以下、好ましくは3mm以下である。即ち凝固
ままの状態の結晶粒を小さくし、さらに凝固後の
冷却過程でα相の粒成長や、γ相の析出を防止す
るため、出来るだけ急冷する必要があり、そのた
めには鋳片の厚みは薄い程好ましいが、1mm未満
の鋳片を鋳造する場合は、生産性が低く、経済的
に好ましくないので下限を1mmとするものであ
る。また、上限を30mm以下、好ましくは3mm以下
としたのは、これを超える鋳片厚みでは、鋳造ま
まの状態での結晶粒径が大きく、また通常の方法
で急冷しても、冷却速度が速くならず、冷却過程
でγ相の析出を防止することや、粒成長の防止が
困難な場合が多くなるからである。鋳片厚みが30
mm以下であれば、熱間圧延を行う場合も、粗圧延
工程は全く不必要で、粗圧延工程の省略が可能と
なることは言うまでもない。又鋳片厚みが10mm以
下、好ましくは5mm以下の場合は、仕上熱延工程
も省略出来る。
また本発明で、γ相析出完了温度(通常、約
1000℃)までの鋳片の冷却速度を空冷以上の冷却
速度、好ましくは100℃/sec以上としたのは、γ
相の析出防止および粒成長防止を狙つたものであ
り、空冷以上の冷却速度ならばγ相の析出は完全
とはいえないが防止可能であり、100℃/sec以上
の冷却速度ならば実質的に防止可能であることに
よる。
また1000℃〜700℃の温度域で10秒間以上の析
出処理を施すのは急速冷却によつて、α相中に過
飽和に固溶しているC、N、S等を、炭窒化物、
硫化物の形で析出させ、冷延性および最終製品の
伸びを増し、降伏点を下げるためであり、1000℃
以上では、溶解度が大きく効果的でなくかつ粒成
長が起こり、逆にリジング特性の劣化を来すので
上限を1000℃としたものであり、700℃以上とし
たのは、これ未満の温度では、析出速度が遅く効
果的でないので下限を700℃とした。また10秒間
以上としたのはこれより短い時間では保定効果が
ないことによる。
通常、上記析出処理は700℃以上、好ましくは
800℃以上の高温で鋳片を捲取ることによつて達
成できるものである。
本発明において冷却過程で析出するγ量は全く
ないことが好ましいが、このγ量を全γ量(全温
度を通じて最大量の平衡γ量)の10%以下として
も本発明の目的は達成できる。即ち、この程度の
γ量であれば熱延板焼鈍を省略しても冷延性に支
障がなく、また、リジング特性の改善にも問題が
ないからである。
リジング特性を改善するには、凝固のままの結
晶粒径を小さくし、かつ前述の如くγ相を微細分
散させることが好ましいが、凝固後の冷却過程に
全γ量の10%以上が析出すると、その後γ相が析
出すべき温度域に再加熱した場合も、すでに析出
しているγ相が新たに析出するγ相の析出サイト
となるため、今迄析出していたγ相の位置とは異
なつた新たなサイトに析出するγ相の割合が減少
し、その結果γ相の別細分散効果が少なくなり、
リジング特性の改善効果が減少するが、冷却過程
におけるγ相の析出が10%以下であればかかる問
題は生ぜず、リジング特性改善効果が期待でき
る。
本発明に従つてCr系薄肉鋳片を凝固温度から
γ相析出終了温度以下まで、α相領域内にあるよ
うに冷却した後、再びα+γ2相に加熱する目的
は、リジング特性改善のために、γ相を微細分散
析出させることにあるが、その場合全γ量の少な
くとも30%以上のγ相が析出するまでこの温度領
域に保持するのが有利である。けだしリジング特
性の改善には、出来るだけ多量のγが、均質かつ
微細に析出していることが望ましいが、このよう
な熱処理によつて全γ量の少なくとも30%以上の
γ相が析出すれば、リジング特性改善効果が顕著
となるからである。
また本発明に従いγ相の析出熱処理の前に圧下
を加えると、γ相の析出が促進され、且つ、析出
サイトが増して微細化されるが、その場合の圧下
率は10%以上がよい。これ未満の圧下ではγ相の
析出促進、微細化の効果が殆んど期待されないか
らであり、圧下率は高い程効果的であるが、90%
以上では効果が飽和する。この加工を与える時期
はγ相析出前なら、凝固直後でも、急冷後γ相へ
の再加熱直前でもいづれの時期でも効果があるの
はいうまでもない。
α+γ2相域に再加熱する場合、急冷により、
α相中に過飽和に固溶したC、N、はγ相中に移
動するので、前述の如き析出処理は必ずしも必要
ではない。
しかし、前述の如き析出処理を引続き行なうこ
とは、γ→α変態が部分的に生じ、かつ固溶C、
N、S量が低下するので冷延性が向上し、成品伸
びが向上し、降伏強度を低下できる。
本発明において、ザクを防止する目的では、5
%以上の加工を800℃以上で加えればよく、加工
による再結晶を促進するためには、25%以上、好
ましくは、35%以上の加工が必要である。
以上の如く加工熱処理された薄肉鋳片は、引続
き熱間圧延を行つた後コイルとして捲取り、冷間
圧延、焼鈍して薄板としてもよいし、熱間圧延を
行わずに直接冷間圧延、焼鈍を行つてもよいが、
目標とする薄板の品質に従つて冷間圧延、焼鈍条
件を決定しなければならないのは言うまでもな
い。尚本発明が対象とする鋼成分は、フエライト
単相鋼でもよいが、下式に基づいて算定されるγ
量(このγ量は、全温度範囲を通じて最大のγ量
を示す指標としての値である)を含有している成
分組成の鋼であることが好ましく、この場合γ量
は100を超えないように成分系を調整する必要が
ある。
γ%=420×〔C%〕+470×〔N%〕+7
×〔Mn%〕−11.5×〔Cr%+Si%〕−49
×〔Ti%〕−52×〔Al%〕+189
(実施例)
実施例 1
表1に示す成分のCr鋼を双ロール法で厚さ4
mmの薄肉鋳片に鋳造後、直ちに水冷した後850℃
で捲取つて薄肉鋳片コイルとした。比較のため鋳
造後室温まで空冷して捲取つたコイルも製造し
た。このようにして製造した薄肉鋳片を冷間圧延
したが、鋳造後直ちに水冷し850℃で捲取つたも
のは、冷却過程でγ相の析出がなく、冷間圧延中
の耳割れや、冷間圧延中の厚み変動も少なく、良
好な冷延性を示したが、空冷したものは、マルテ
ンサイトが形成され、冷延性が悪かつた。
(Industrial Application Field) The present invention relates to a method for manufacturing thin-walled Cr-based stainless steel slabs. (Prior art) Stainless steel thin steel plates are, for example, disclosed in Japanese Patent Application Laid-open No. 55-97430.
As described in the publication, slabs continuously cast to a thickness of around 200 mm are roughly rolled or heated to 1200°C, then hot finish rolled to form hot rolled sheets, and hot rolled sheets are produced in a bell-shaped annealing furnace. The product is annealed, cold rolled, and finished annealed. (Problems to be solved by the invention) As mentioned above, in the known technology, the thickness of the slab is large;
It takes a lot of energy to form a hot-rolled sheet into a specified shape, and since the α' phase is formed in the slab as hot-rolled, it is necessary to form a bell-shaped slab to break it down and improve cold-rollability. Requires long annealing in an annealing furnace. (Means for solving the problems) The present invention provides the following features in the ingot making of Cr-based stainless steel:
To produce a slab in which the γ phase does not precipitate by continuously casting molten steel into a thin slab and cooling the slab to a temperature within the α phase region at which the precipitation of the γ phase ends. The main points are:
By using such a slab as a starting material, there is no need for various energy and equipment to make a specified hot-rolled sheet, and even if the process equivalent to hot-rolled sheet annealing is omitted, it can be made with good cold rollability and ridging properties. The effect of being able to manufacture thin steel sheets is achieved. The present invention will be explained in detail below. The first object of the present invention is to omit the step equivalent to hot-rolled sheet annealing, which is performed to improve cold rolling properties, in the production of Cr-based stainless steel thin sheets. Among Cr-based stainless steel sheets, steel types such as SUS410 contain a large amount of hard phase generated by the transformation of the γ phase in the as-hot-rolled state, so if they are cold-rolled in this state, , hot-rolled sheet annealing causes defects such as cold-rolling breakage, uneven rolling reduction during cold rolling, and large fluctuations in the thickness in the longitudinal direction of the coil.
It is necessary to perform hot-rolled sheet annealing to separate this hard phase into ferrite + carbide. As a result of research into ways to omit this hot-rolled sheet annealing step, the present inventors have found that, in order to prevent the formation of the γ phase, which causes the formation of hard phases, the present inventors Cool it so that γ
It has been discovered that if a phase-free hot rolled sheet is produced, no hard phase is formed, and therefore the process corresponding to the hot rolled sheet annealing described above becomes unnecessary. i.e. thickness
In the case of a slab of around 200 mm, even if the surface of the slab is cooled by the usual method after casting, the cooling rate is limited by the thermal conductivity of the slab itself, and the precipitation of the γ phase during the solidification process may occur. Although it cannot be prevented, by limiting the thickness of the slab to a predetermined thickness and cooling it so that it is within the α phase region after solidification, the α phase can be reduced without precipitating the γ phase.
This makes it possible to bring it to regions where phases and carbides exist. In the α phase + carbide region, C, N, S, etc. supersaturated in solid solution in the α phase are
Precipitation treatment is required to form carbonitrides and sulfides. If such precipitation treatment is not performed, there will be drawbacks such as significant work hardening during cold rolling, and low elongation and high yield point in the final product. That is, in order to improve cold rollability, instead of hot-rolled sheet annealing to decompose the α' phase formed from the γ phase into α+ carbide, heat treatment is performed only for precipitation treatment to precipitate C, N, S, etc. from supersaturated α. If this is carried out, the cold rollability will be improved, and this precipitation treatment can be done in a shorter time than the reaction of α′ → α + carbide, and can be done in the normal rolling process, so no special heat treatment process is required. be. A second object of the present invention is to provide a technique for producing a thin plate having improved workability, particularly ridging properties, using a thin slab as a starting material. In order to improve ridging properties, it is necessary that the size of colonies (a group of crystal grains having similar orientations) is small, that the colonies are randomly distributed, and that the crystal grain size is also relatively small. For this purpose, it is necessary to reduce the crystal grain size of the slab and to prevent an increase in locony size due to grain boundary movement during the cooling process after solidification. Since conventional slabs have a large thickness of 100 mm or more, it is difficult to control the solidification rate during casting, and it is impossible to reduce the crystal grain size in the as-cast state. In addition, the cooling rate of the slab after casting is difficult due to the large thickness of the slab, which causes an increase in colony size due to grain boundary movement in the high temperature range during cooling, and the hot rolling process It is necessary to recrystallize it to reduce the colony size. However, in the case of a thin slab as in the present invention, by limiting the thickness of the slab to 10 mm or less, preferably 3 mm or less, the solidification rate after casting can be increased, so it is possible to reduce the crystal grains of the slab. This is possible, and further, by increasing the cooling rate after solidification as in the present invention, the colony size can be reduced. SUS430 with components that form α+γ2 phase at high temperatures
In Cr-based stainless steels, such as Cr stainless steels, it is not possible to refine the colony size in the as-cast state.In order to refine the colony size in slabs of normal thickness, it is necessary to finely disperse the γ phase. γ
Techniques for finely dispersing phases include, for example, a technique in which a cast slab is reheated to an α single phase region, then subjected to a large pressure reduction, and then cooled to an α + γ two phase region (Japanese Patent Laid-Open Publication No. 11827/1982); Technology for heating hot-rolled sheets to the α+γ2 phase region,
Further, there are prior art techniques such as a technique (Japanese Unexamined Patent Publication No. 83724/1983) of heating to the α+γ2 phase region between rough rolling and finish rolling. In the case of the method of reheating to the α single phase region, the crystal grains of the α phase are coarsened due to reheating to a high temperature, so that the effect of improving the ridging properties, which is the final objective, is small. The method of reheating a hot-rolled sheet to the α+γ2 phase region is as follows:
Although the effect of improving ridging properties is significant, cold rollability deteriorates and surface defects such as sparkling scratches are likely to occur. The method of heating to the α+γ2 phase region between rough rolling and finish rolling has a large effect on improving ridging properties.
This is the most excellent method among the above three methods, as there is no deterioration in cold rollability or occurrence of surface defects such as sparkling scratches. The present inventors improved and developed these measures and found a method for finely dispersing the γ phase. That is, after solidification is completed, the slab is cooled in the α phase region to prevent the precipitation of the γ phase, and then reheated to the α+γ phase region to cause the precipitation of the γ phase. Compared to the case where the γ phase is precipitated during the solidification process, the α phase is
Since the γ phase precipitates after the fine precipitation of precipitates such as Cr carbides, these precipitates become sites for γ precipitation, and since γ phase precipitation occurs at low temperatures, the growth rate of the γ phase is slow. Therefore, compared to the case where the γ phase is precipitated during the cooling process from a high temperature, it becomes possible to precipitate and disperse the fine γ phase at a higher density. In this case, by applying processing to the α+γ2 phase region before reheating, the number of precipitation sites for the γ phase increases, so that the fine dispersion of the γ phase is performed more effectively. In the present invention, another purpose of adding processing is to press the dents produced by rapid solidification to prevent cold rolling breakage, and to promote recrystallization at high temperatures by processing. In this case, although it is effective to apply a reduction of 5% or more to compress the Zaku, a reduction of 25% or more, preferably 35% or more is required to promote recrystallization by processing. Next, the reasons for limiting the components of the starting materials of the present invention will be explained. The reason why Cr is set to 8% or more is because corrosion resistance is poor if the Cr content is less than this. Corrosion resistance improves as the amount of Cr added increases, but if it exceeds 30%, the effect is small and cold rollability deteriorates. Considering economic efficiency, a larger amount of Cr is not preferable, so 30% was set as the upper limit. The reason for setting the C content to be 0.001% or more is because it is difficult to melt a starting material with a C content lower than this using a normal method. The greater the amount of C added, the better the ridging properties will be, but if added in excess of 0.5%, cold rollability and r-value will deteriorate, so the upper limit should be set at 0.5%.
%. The r value improves as the amount of Al added increases, but 0.5%
The upper limit was set at 0.5% because the effect would be saturated and it would be uneconomical to add more than this amount.The lower limit was set at 0.001% because if the amount of Al is less than this, O 2 will increase significantly.
Since this is not preferable, the lower limit is set at 0.001%. The higher the amount of N added, the better the ridging properties will be, but adding more than 0.5% will cause blisters, etc., so the upper limit is set at 0.5%.
The lower the value is 0.004% or less, the better the r value improves, but
Less than 0.001% cannot be melted using normal methods.
The lower limit is 0.001%. The components of the starting material in the present invention have a Cr of 8 to 30
% range, any element that becomes α+ (carbide) at room temperature is within the scope of the present invention, and α+ (carbide) in all temperature ranges.
Even in the case of single-phase component composition, grain growth can be prevented by rapidly cooling the slab, but in this case, C, N, S, etc. become supersaturated solid solutions and the slab becomes abnormal. Because it hardens, these supersaturated O,
By precipitating N and S, it is possible to manufacture slabs with small grain size and ductility, which is included in the scope of the present invention. However, the components that achieve the main purpose of the present invention include: Needless to say, it is a component system that forms α and γ2 phases at high temperatures. The thickness of the slab in the starting material of the present invention is 1 mm or more
It is 30 mm or less, preferably 3 mm or less. In other words, it is necessary to cool the slab as rapidly as possible in order to reduce the size of crystal grains in the as-solidified state and to prevent grain growth of the α phase and precipitation of the γ phase during the cooling process after solidification. The thinner it is, the more preferable it is, but when casting slabs less than 1 mm, productivity is low and it is economically unfavorable, so the lower limit is set to 1 mm. In addition, the upper limit is set to 30 mm or less, preferably 3 mm or less, because if the slab thickness exceeds this, the crystal grain size in the as-cast state will be large, and even if it is rapidly cooled by the usual method, the cooling rate will be too fast. This is because it is often difficult to prevent precipitation of the γ phase or grain growth during the cooling process. Slab thickness is 30
It goes without saying that if it is less than mm, the rough rolling step is completely unnecessary even when hot rolling is performed, and the rough rolling step can be omitted. Furthermore, if the thickness of the slab is 10 mm or less, preferably 5 mm or less, the finishing hot rolling process can also be omitted. In addition, in the present invention, the γ phase precipitation completion temperature (usually about
γ
This is aimed at preventing phase precipitation and grain growth; if the cooling rate is higher than air cooling, precipitation of the γ phase can be prevented, although not completely, and if the cooling rate is 100℃/sec or higher, it can be prevented substantially. By being preventable. In addition, the precipitation treatment for 10 seconds or more in the temperature range of 1000°C to 700°C is performed by rapid cooling, which removes C, N, S, etc., which are supersaturated solid solution in the α phase, into carbonitrides,
This is to precipitate in the form of sulfides, increase cold rollability and elongation of the final product, and lower the yield point, and at 1000℃
In the above, the upper limit was set at 1000℃ because the solubility is large and it is not effective, grain growth occurs, and the ridging properties deteriorate. Since the precipitation rate was slow and ineffective, the lower limit was set at 700°C. Furthermore, the reason why the duration was set to 10 seconds or more is that shorter durations have no retention effect. Usually, the above precipitation treatment is carried out at temperatures above 700℃, preferably
This can be achieved by rolling the slab at a high temperature of 800°C or higher. In the present invention, it is preferable that no amount of γ precipitates during the cooling process, but the object of the present invention can be achieved even if the amount of γ is 10% or less of the total amount of γ (maximum amount of equilibrium γ throughout the entire temperature). That is, if the amount of γ is at this level, there will be no problem in cold rollability even if hot-rolled sheet annealing is omitted, and there will be no problem in improving ridging properties. In order to improve ridging properties, it is preferable to reduce the crystal grain size as solidified and to finely disperse the γ phase as described above, but if more than 10% of the total γ amount precipitates during the cooling process after solidification, , even if the temperature is then reheated to the temperature range where the γ phase should precipitate, the already precipitated γ phase becomes the precipitation site for the newly precipitated γ phase, so the position of the γ phase that has been precipitated until now is The proportion of γ phase precipitated at different new sites decreases, and as a result, the effect of separate dispersion of γ phase decreases.
Although the effect of improving the ridging properties is reduced, if the precipitation of γ phase during the cooling process is 10% or less, this problem does not occur and the effect of improving the ridging properties can be expected. According to the present invention, the purpose of cooling the Cr-based thin slab from the solidification temperature to below the γ-phase precipitation termination temperature so that it is in the α-phase region and then heating it again to the α+γ2 phase is to improve the ridging properties. The objective is to precipitate the γ phase in a finely dispersed manner, and in this case it is advantageous to maintain this temperature range until at least 30% of the total γ amount of the γ phase is precipitated. In order to improve the ridging properties, it is desirable that as much γ as possible is precipitated homogeneously and finely, but if at least 30% of the total γ amount is precipitated by such heat treatment, This is because the effect of improving ridging characteristics becomes remarkable. Further, according to the present invention, when rolling is applied before the heat treatment for precipitation of the γ phase, precipitation of the γ phase is promoted, and the number of precipitation sites is increased and refined, but the rolling reduction ratio in this case is preferably 10% or more. This is because if the rolling reduction is less than this, the effect of promoting the precipitation of the γ phase and refining is hardly expected, and the higher the rolling reduction, the more effective it is, but 90%
Above that, the effect is saturated. It goes without saying that this processing can be applied any time before the precipitation of the γ phase, immediately after solidification, or immediately before reheating to the γ phase after rapid cooling, which is effective. When reheating to the α + γ2 phase region, by rapid cooling,
Since the supersaturated solid solution of C and N in the α phase moves into the γ phase, the above-mentioned precipitation treatment is not necessarily required. However, if the precipitation treatment as described above is continued, γ→α transformation will occur partially, and solid solution C,
Since the amounts of N and S are reduced, cold rollability is improved, product elongation is improved, and yield strength can be reduced. In the present invention, for the purpose of preventing scratches, 5
% or more processing at 800° C. or higher, and in order to promote recrystallization by processing, processing of 25% or more, preferably 35% or more is necessary. The thin slab that has been processed and heat treated as described above may be subsequently hot rolled, then wound up as a coil, cold rolled, and annealed to form a thin plate, or it may be directly cold rolled without hot rolling. Annealing may be performed, but
Needless to say, cold rolling and annealing conditions must be determined according to the target quality of the thin plate. The steel composition targeted by the present invention may be ferrite single phase steel, but the γ calculated based on the following formula
(This γ amount is a value as an index indicating the maximum γ amount throughout the entire temperature range).In this case, the γ amount should not exceed 100. It is necessary to adjust the component system. γ%=420×[C%]+470×[N%]+7×[Mn%]−11.5×[Cr%+Si%]−49×[Ti%]−52×[Al%]+189 (Example) Implementation Example 1 Cr steel with the composition shown in Table 1 was processed by the twin roll method to a thickness of 4 mm.
After casting into a thin slab of mm, immediately cooled with water to 850℃.
It was wound into a thin-walled slab coil. For comparison, we also produced a coil that was air-cooled to room temperature after casting and then wound. Thin slabs produced in this way were cold-rolled, but those that were water-cooled immediately after casting and rolled at 850℃ showed no precipitation of γ phase during the cooling process, and no edge cracks or cold-rolling occurred during cold rolling. Thickness variation during rolling was small and good cold rollability was exhibited, but martensite was formed in the air-cooled steel sheet, resulting in poor cold rollability.
【表】
実施例 2
表2に示す成分のSUS430鋼を双ロール法で厚
さ10mmの薄肉鋳片に鋳造後、直ちに水冷した。比
較のため鋳造後空冷したもの及び、厚さ200mmの
鋳片を公知の方法で試作した。本発明に従つて水
冷したものは、γ相の析出がなく、フエライト単
相となつていたが、空冷したものや、公知の方法
で鋳造したスラブはα+α′2相組織となつていた。
こうして試作した厚さ10mmの薄肉鋳片に30%の圧
下を加えてからα+γ2相に再加熱した後、熱間
圧延して厚さ3mmの熱延板とし、次いで常法に従
つて冷間圧延、焼鈍を行つた。本発明に従つた薄
板はリジングが殆んど観察されなかつたが、空冷
したものはリジングが著しく大きかつた。[Table] Example 2 SUS430 steel having the components shown in Table 2 was cast into a thin slab with a thickness of 10 mm by the twin roll method and immediately cooled with water. For comparison, a cast piece that had been air cooled after casting and a slab with a thickness of 200 mm were produced using a known method. The slabs cooled by water according to the present invention had a single ferrite phase without precipitation of the γ phase, whereas the slabs cooled by air or cast by a known method had an α+α′2 phase structure.
The prototype thin slab with a thickness of 10 mm was subjected to a 30% reduction and then reheated to α+γ2 phase, then hot-rolled into a hot-rolled plate with a thickness of 3 mm, and then cold-rolled according to a conventional method. , annealing was performed. In the thin plate according to the present invention, almost no ridging was observed, but in the air-cooled plate, ridging was significantly large.
【表】
実施例 3
表3に示す成分の17Cr鋼を厚さ7mmの薄肉鋳
片に鋳造後、γ相の析出する以前に圧延加工を加
えて厚さ4mmとした後、引続きα相領域で冷却し
て850℃で捲取つてコイルとした。比較のため、
7mmの鋳片に鋳造後、γ相が析出開始した後圧延
加工して厚さ4mmの鋳片としたものも試作した。
これらの鋳片は、引続き冷間圧延、焼鈍して薄板
とした。本発明に従つて鋳片としたものは、ザク
性欠陥もなく冷延性も良好で、最終成品のr値は
γで1.10、リジング特性は15μmでありともに良
好であつたが、比較材は、冷間圧延前に硬くても
ろいα′相が存在し、冷間圧延時に耳割れが発生
し、冷延性が劣化した。[Table] Example 3 After casting 17Cr steel with the composition shown in Table 3 into a thin slab with a thickness of 7 mm, it was rolled to a thickness of 4 mm before the γ phase precipitated, and then it was further rolled in the α phase region. It was cooled and rolled up at 850°C to form a coil. For comparison,
A prototype slab with a thickness of 4 mm was also produced by casting into a slab of 7 mm and rolling it after the gamma phase started to precipitate.
These slabs were subsequently cold rolled and annealed into thin sheets. The slab made according to the present invention had no roughness defects and good cold rollability, and the final product had an r value of 1.10 in γ and a ridging property of 15 μm, both of which were good. A hard and brittle α' phase existed before cold rolling, and edge cracking occurred during cold rolling, deteriorating cold rollability.
【表】
実施例 4
表4に示す成分の17Cr鋼を厚さ15mmの鋳片に
鋳造後、α相中で150℃/secの冷却速度で800℃ま
で冷却後、α+γ2相域である1100℃の温度に再
加熱後、圧延加工を加えて厚さ4mmの熱延板とし
た。比較のため厚さ15mmの鋳片に鋳造後、そのま
ま大気中で冷却し、1100℃の温度に達した後、圧
延加工を加えて厚さ4mmの熱延板とした。このよ
うにして試作した熱延板は公知の方法で薄板とし
たが、本発明の方法に従つてα相中で冷却後、α
+γ2相域に再加熱後圧延加工したものは、比較
材と比べて著しく良好なリジング特性(10μm)
を示した。尚、比較材は28μmであつた。[Table] Example 4 After casting 17Cr steel with the composition shown in Table 4 into a slab with a thickness of 15 mm, it was cooled to 800°C at a cooling rate of 150°C/sec in the α phase, and then cooled to 1100°C, which is the α+γ2 phase region. After reheating to a temperature of , rolling was performed to obtain a hot rolled sheet with a thickness of 4 mm. For comparison, a slab with a thickness of 15 mm was cast, then cooled in the air as it was, and after reaching a temperature of 1100°C, it was rolled into a hot rolled plate with a thickness of 4 mm. The hot-rolled sheet prototyped in this way was made into a thin sheet by a known method, and after cooling in the α phase according to the method of the present invention, α
The material that has been reheated and rolled to the +γ2 phase region has significantly better ridging properties (10 μm) than the comparative material.
showed that. The comparative material had a thickness of 28 μm.
【表】
実施例 5
表5に示す成分の17%Cr鋼を厚さ3mmの鋳片
に鋳造後、100℃/secの冷却速度で1000℃まで冷
却した後、850℃の温度で捲取つた。
比較のため、100℃/secの冷却速度で室温まで
急冷した鋳片も製造した。
850℃で捲取つた材料は、その後80%の冷間圧
延を行ない、850℃×2分間の焼鈍を施して成品
とした。この成品は、リジング約15μm、r値0.8
と良好であつた。
これに比し上記室温まで急冷したものは、同じ
工程で処理したけれども、冷延破断がおきて、歩
留低下が大きかつた。[Table] Example 5 17% Cr steel with the composition shown in Table 5 was cast into a slab with a thickness of 3 mm, cooled to 1000°C at a cooling rate of 100°C/sec, and then rolled at a temperature of 850°C. . For comparison, slabs were also produced that were rapidly cooled to room temperature at a cooling rate of 100°C/sec. The material rolled at 850°C was then subjected to 80% cold rolling and annealed at 850°C for 2 minutes to form a finished product. This product has a ridding of approximately 15 μm and an r value of 0.8.
It was good. In contrast, when the material was rapidly cooled to room temperature, although it was processed in the same process, cold rolling breakage occurred and the yield was greatly reduced.
【表】
実施例 6
表6に示す成分の17%Cr鋼を3mmの鋳片に鋳
造後、1200℃までを20℃/sec、1200℃から1000℃
までを100℃/secの冷却速度で冷却した後、900℃
で捲取り、空冷よりも遅い速度で冷却するよう保
温カバーをかけて冷却した。
比較のため、鋳造後、そのまま室温まで空冷し
た試片も作つた。
このようにして鋳造した鋳片を0.4mmまで冷間
圧延した後、900℃×40秒間の仕上焼鈍を行なつ
て成品とした。本発明によつて製造した成品はリ
ジング特性17μm、全伸び27%、降伏強度35Kg/
mm2と良好であつた。これに比し、鋳造後、そのま
ま室温まで空冷したものは、全伸び18%、リジン
グ28μmで伸び、リジング特性ともよくなかつ
た。[Table] Example 6 After casting 17% Cr steel with the composition shown in Table 6 into a 3 mm slab, it was heated at 20°C/sec up to 1200°C and from 1200°C to 1000°C.
After cooling up to 900℃ at a cooling rate of 100℃/sec
It was rolled up and cooled with a heat insulating cover so that it cooled at a slower rate than air cooling. For comparison, we also made specimens that were air-cooled to room temperature after casting. The thus cast slab was cold rolled to 0.4 mm and then final annealed at 900°C for 40 seconds to produce a finished product. The product manufactured according to the present invention has a ridging property of 17 μm, a total elongation of 27%, and a yield strength of 35 kg/
It was good at mm2 . In contrast, those that were air-cooled to room temperature after casting had a total elongation of 18% and a ridging of 28 μm, and the ridging properties were also poor.
【表】
(発明の効果)
本発明に従えば、冷延性やリジング特性の良好
なCr系ステンレス鋼薄板を、粗圧延工程、仕上
圧延工程および熱延板焼鈍工程を省略して製造す
ることが可能となり、しかも連続熱間圧延機の如
き大型設備を必要としないので、経済的効果は極
めて大きく、従つて本発明は産業上著しく有用な
発明である。[Table] (Effects of the Invention) According to the present invention, a Cr-based stainless steel thin plate with good cold rollability and ridging properties can be produced by omitting the rough rolling process, finish rolling process, and hot rolled sheet annealing process. In addition, since large-scale equipment such as a continuous hot rolling mill is not required, the economic effect is extremely large, and therefore, the present invention is extremely useful industrially.
Claims (1)
N:0.001〜0.5%およびAl:0.001〜0.5%を主成
分とし、残部が実質的にFeからなるCr系ステン
レス鋼薄肉鋳片の製造方法であつて、鋳造後の鋳
片を、凝固温度からγ相析出終了温度まで、100
℃/s以上の冷却速度で冷却し、次いで700℃以上
1000℃以下のα単相の温度域で10秒間以上の析出
処理を施すことを特徴とするCr系ステンレス鋼
薄肉鋳片の製造方法。 2 重量で、Cr:8〜30%、C:0.001〜0.5%、
N:0.001〜0.5%およびAl:0.001〜0.5%を主成
分とし、残部が実質的にFeからなるCr系ステン
レス鋼薄肉鋳片の製造方法であつて、鋳造後の鋳
片を、凝固温度からγ相析出終了温度まで、100
℃/s以上の冷却速度で冷却することおよび前記冷
却過程において或は冷却後に前記鋳片に圧延加工
を施し、次いで700℃以上1000℃以下のα単相の
温度域で10秒間以上の析出処理を施すことを特徴
とするCr系ステンレス鋼薄肉鋳片の製造方法。 3 重量で、Cr:8〜30%、C:0.001〜0.5%、
N:0.001〜0.5%およびAl:0.001〜0.5%を主成
分とし、残部が実質的にFeからなるCr系ステン
レス鋼薄肉鋳片の製造方法であつて、鋳造後の鋳
片を、凝固温度からγ相析出終了温度まで、100
℃/s以上の冷却速度で冷却し、次いでα+γ二相
域まで加熱してγ相を析出させることを特徴とす
るCr系ステンレス鋼薄肉鋳片の製造方法。 4 重量で、Cr:8〜30%、C:0.001〜0.5%、
N:0.001〜0.5%およびAl:0.001〜0.5%を主成
分とし、残部が実質的にFeからなるCr系ステン
レス鋼薄肉鋳片の製造方法であつて、鋳造後の鋳
片を、凝固温度からγ相析出終了温度まで、100
℃/s以上の冷却速度で冷却することおよび前記冷
却過程において或は冷却後に前記鋳片に圧延加工
を施すことおよび、かくして得られた薄肉鋳片を
α+γ二相域まで加熱してγ相を析出させること
を特徴とするCr系ステンレス鋼薄肉鋳片の製造
方法。[Claims] 1. By weight, Cr: 8-30%, C: 0.001-0.5%,
A method for producing thin-walled Cr-based stainless steel slabs whose main components are N: 0.001 to 0.5% and Al: 0.001 to 0.5%, with the remainder being substantially Fe, the method comprising: Up to the end temperature of γ phase precipitation, 100
Cool at a cooling rate of ℃/s or higher, then 700℃ or higher
A method for producing thin-walled Cr-based stainless steel slabs, characterized by performing precipitation treatment for 10 seconds or more in an α single-phase temperature range of 1000°C or less. 2 By weight, Cr: 8-30%, C: 0.001-0.5%,
A method for producing thin-walled Cr-based stainless steel slabs whose main components are N: 0.001 to 0.5% and Al: 0.001 to 0.5%, with the remainder being substantially Fe, the method comprising: Up to the end temperature of γ phase precipitation, 100
Cooling at a cooling rate of ℃/s or more, and rolling the slab during or after the cooling process, followed by precipitation treatment for 10 seconds or more in the α single phase temperature range of 700℃ or higher and 1000℃ or lower. A method for manufacturing thin-walled Cr-based stainless steel slabs, characterized by subjecting them to the following steps: 3 By weight, Cr: 8-30%, C: 0.001-0.5%,
A method for producing thin-walled Cr-based stainless steel slabs whose main components are N: 0.001 to 0.5% and Al: 0.001 to 0.5%, with the remainder being substantially Fe, the method comprising: Up to the end temperature of γ phase precipitation, 100
A method for producing a thin-walled Cr-based stainless steel slab, characterized by cooling at a cooling rate of ℃/s or more, and then heating to an α+γ two-phase region to precipitate the γ phase. 4 By weight, Cr: 8-30%, C: 0.001-0.5%,
A method for producing thin-walled Cr-based stainless steel slabs whose main components are N: 0.001 to 0.5% and Al: 0.001 to 0.5%, with the remainder being substantially Fe, the method comprising: Up to the end temperature of γ phase precipitation, 100
cooling at a cooling rate of ℃/s or more; rolling the slab during or after the cooling process; and heating the thus obtained thin slab to an α+γ two-phase region to remove the γ phase. A method for producing thin-walled Cr-based stainless steel slabs, characterized by precipitation.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP86309086A EP0247264B1 (en) | 1986-05-24 | 1986-11-20 | Method for producing a thin casting of cr-series stainless steel |
| DE8686309086T DE3686155T2 (en) | 1986-05-24 | 1986-11-20 | METHOD FOR PRODUCING A THIN CASTING PIECE MADE OF STAINLESS STEEL CR STEEL. |
| US06/934,108 US4709742A (en) | 1986-05-24 | 1986-11-24 | Method for producing a thin casting of Cr-series stainless steel |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11187985 | 1985-05-24 | ||
| JP60-111879 | 1985-05-24 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6254017A JPS6254017A (en) | 1987-03-09 |
| JPH0159330B2 true JPH0159330B2 (en) | 1989-12-15 |
Family
ID=14572441
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11839086A Granted JPS6254017A (en) | 1985-05-24 | 1986-05-24 | Production of thin-walled cr stainless steel slab |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6254017A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02275688A (en) * | 1988-03-19 | 1990-11-09 | Ricoh Co Ltd | Semiconductor optical integrated element |
| JP2815603B2 (en) * | 1989-03-07 | 1998-10-27 | 新日本製鐵株式会社 | Method for producing Cr-based stainless steel sheet using thin casting method |
| FR2790485B1 (en) * | 1999-03-05 | 2002-02-08 | Usinor | CONTINUOUS CASTING PROCESS BETWEEN CYLINDERS OF HIGH-DUCTILITY FERRITIC STAINLESS STEEL STRIPS, AND THIN STRIPS THUS OBTAINED |
-
1986
- 1986-05-24 JP JP11839086A patent/JPS6254017A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6254017A (en) | 1987-03-09 |
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