JPH0154409B2 - - Google Patents
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- Publication number
- JPH0154409B2 JPH0154409B2 JP60268349A JP26834985A JPH0154409B2 JP H0154409 B2 JPH0154409 B2 JP H0154409B2 JP 60268349 A JP60268349 A JP 60268349A JP 26834985 A JP26834985 A JP 26834985A JP H0154409 B2 JPH0154409 B2 JP H0154409B2
- Authority
- JP
- Japan
- Prior art keywords
- blowing
- oxygen
- gas
- oxidizing gas
- stainless 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.)
- Expired
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/005—Manufacture of stainless steel
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Treatment Of Steel In Its Molten State (AREA)
- Carbon Steel Or Casting Steel Manufacturing (AREA)
Description
(産業上の利用分野)
転炉又はこれに類似の精錬容器を用いるステン
レス粗溶鋼の脱炭精錬に関して、簡単な設備によ
り経済的な操業を可能にする手法についての開発
研究の成果をここに提案する。
(従来の技術)
ステンレス鋼の溶製に関しては、日本鉄鋼協会
編「鉄鋼便覧」第2巻、製銑・製鋼p693〜728に
詳述され、その代表例は、転炉・AOD炉のよう
な底吹き羽口を有する反応容器内に、電気炉で溶
解したステンレス粗溶鋼を装入し、その炉底羽口
から酸素あるいは酸素とアルゴンの混合ガスを吹
き込んで脱炭する方法である。
一方最近、特開昭58−130216号公報に開示され
ているように炉底羽口より酸素、あるいは酸とア
ルゴン、または、酸素と窒素の混合ガスを鋼浴に
吹込むと同時に、上吹ランスより酸素とアルゴ
ン、または酸素と窒素の混合ガスを吹込む方法
や、また特公昭59−21367号公報では、「含クロム
鋼浴の浴面下に酸素及び不活性ガスを吹込んで脱
炭反応を行わせると同時に、……純酸素若しくは
……酸素を含む酸素含有ガスを浴面上に吹込む」
方法も開示されている。
以上の方法では脱炭用の酸素を炉底羽口より吹
込むことを必須条件としている。
この炉底羽口は通常2重管構造とされ、AOD
炉では内管からアルゴンと酸素の混合ガスを、内
管と外管の間隙からアルゴンを供給し、底吹き転
炉の場合は、内管と外管の間隙から炭化水素ガス
を供給する。
(発明が解決しようとする問題点)
上述の従来法では、酸素を炉底羽口から供給す
るため、羽口が溶鋼の酸化発熱を受け高温となる
ため溶損する。このため羽口寿命が炉体寿命を決
定する大きな要因であり、生産性の阻害や耐火物
使用量増加を引き起こしていた。
一方、純酸素を上吹きランスから供給すること
も考えられるが、前述の「鉄鋼便覧」p709〜711
に記載されているようにCr酸化が大きく、大量
の高粘性スラグの生成などのために現実的ではな
く工程化されていない。
ここに羽口溶損による炉体寿命に由来した上述
不利を、Cr酸化に伴う損失の如き問題なしに克
服して、簡単な設備による経済的なステンレス鋼
の脱炭精錬を成就する手法を与えることがこの発
明の目的である。
(問題点を解決するための手段)
この発明は、ステンレス粗溶鋼の脱炭精錬法に
関して、ステンレス溶鋼の浴面下に非酸化性ガス
を導入して該溶鋼を撹拌すると同時に、浴面上
に、酸素と非酸化性ガスの混合ガスを吹きつける
ことを上記問題解決の骨子とするものである。
ここで、浴面上に吹きつける混合ガス中の酸素
に対する非酸化性ガスの割合を一定に保つより
も、溶鋼中炭素濃度の低下に従つて増加(非酸化
性ガスの量を増す)することがより望ましい。
この発明によれば、従来方法よりも炉底羽口の
溶損速度が小さいため炉寿命は長くなり、かつ酸
素底吹き法と同等のCr酸化に抑えられるので設
備費や運転費の少ない簡単で経済的なプロセスを
得ることができる。
この発明を実施する際には、第1図に示すよう
な反応容器1が適当であり、通常の上吹き転炉に
ガスを底吹きできる設備とすることが必要であ
る。また上吹きランス2からは酸素と非酸化性ガ
スの混合ガスを吹込めるような配管系3および4
が必要であり、それぞれのガスの流量を制御でき
る装置、例えば流量自動制御弁を設けておくこと
が望ましい。
なお配管系5および6は、後述の比較例を実施
するために設置したものであり、本発明では不要
である。
操業方法の具体要領を述べる。
まず、ステンレス粗溶鋼を上述の機能を有する
上底吹き転炉に装入する。この時、炉底羽口から
は非酸化性ガスを流しておく。次に上吹きランス
を炉内に挿入して酸素あるいは酸素と非酸化性ガ
スの混合ガスを浴面上に吹きつける。上吹きラン
スから供給するガスは鋼中炭素濃度に依存するが
酸素のみで吹錬を開始し、炭素濃度が1%前後に
まで脱炭された時点で酸素と非酸化性ガスの混合
ガスに切替えて、吹錬を継続すると、非酸化性ガ
ス使用量を小さくでき有利である。
このガス種の切替え時点は酸素の供給速度や溶
鋼温度によつて適正範囲が存在するので上記の炭
素濃度が1%前後というのは単に概略の値であ
る。
脱炭反応が進行するにつれて酸素:非酸化性ガ
スの比率を小さくして、熱力学的に優先脱炭が進
みやすい条件とすることが実際的でこのガス比率
の変更方法は、実施例についてあとで示す。
ここに吹錬中に炉底羽口から供給する非酸化性
ガスの流量は一定でもかまわないが、脱炭が優先
して進行する高炭素濃度領域では比較的少量と
し、Crの酸化が始まる炭素濃度になつた時点で
大量に供給する方が、非酸化性ガスの総使用量は
少なくできる。具体的には、Crの酸化が始まる
炭素濃度になつてからは、溶鋼1トン当たり
0.2Nm3/min以上供給するのが望ましく、これに
満たない底吹きガス量では、クロムの酸化が大き
くなり勝ちで経済的でない。
しかし溶鋼1トン当たり1.0Nm3/minを超える
と、撹拌の効果は大きく変化せず、かえつて非酸
化性ガス使用量が多くなるのでこれまた経済的で
ない。
したがつて経済性を考えれば0.2〜1.0Nm3/
minが適切である。
なお吹錬前、吹錬中に添加する副原料は、従来
法と変わらず、生石灰やドロマイトあるいは冷却
材を用いる。
また、いわゆるステンレス粗溶鋼の代わりに、
予め脱りん処理をした溶銑を装入し、ついで炉内
にフエロクロムや含クロム鉱石などのクロム源を
投入することも可能であり、このような場合も単
にステンレス粗溶鋼の表現に含めることとする。
もちろん脱炭精錬後にスラグ中の酸化クロムを
Fe−Siなどの還元剤で還元し同時に脱硫を行う
ことも従来法と同様である。
以上の説明で、非酸化性ガスはクロム分を酸化
しないガスならなんでもよいが、経済性や取扱い
を考慮すると、アルゴン、窒素、水素、炭化水素
ガス、などを単独かあるいは混合して用いるのが
現実的である。
また、吹錬前半を窒素、後半をアルゴンのよう
に切替えて使用することも可能である。
一方、上吹きランスから供給する非酸化性ガス
についても、底吹き用非酸化性ガスと同種であつ
てもまた異種であつてもよい。
(作 用)
この発明の方法でステンレス粗溶鋼の浴面下に
は単に鋼浴の撹拌を専ら司る非酸化性ガスを用い
るため、炉底羽口の損傷ひいては炉底耐火物の損
傷がはるかに少ない。一方浴面上へは優先脱炭を
目的として混合ガスを吹き付けるので、Cr損失
量も従来法と同等である。
(実施例)
実施例 1
第1図に示すような上底吹き転炉を用いて、こ
の発明に従う実施例と、底吹き羽口からのみ混合
ガスを吹き込む比較例1に加えて、特開昭55−
115914号公報に記載されている、底吹き羽口から
は少量の非酸化性ガス、上吹きランスから酸素の
みを吹き付ける比較例2の各場合についての吹錬
を試行した。
ステンレス粗溶鋼は、電気炉溶解したSUS304
(18%Cr−8%Ni−2.5%C)を5トンだけ分湯
して第1図の上底吹き転炉に装入した。
供給した非酸化性ガスはすべてアルゴンとし
た。また混合ガスを用いる吹錬では酸素との混合
比を第1表のように、計算により推定した溶鋼中
炭素濃度により漸次変更した。またこの発明を実
施する際には、第1表の混合ガス比の計算に、底
吹き用のアルゴンは考慮せず、上吹きランスから
のアルゴンのみを用いた。
(Industrial Application Field) We present here the results of research and development on a method that enables economical operation with simple equipment regarding decarburization of crude molten stainless steel using a converter or similar refining vessel. do. (Conventional technology) Stainless steel melting is detailed in the Iron and Steel Handbook, Volume 2, Pigmaking and Steelmaking, pages 693 to 728, edited by the Japan Iron and Steel Institute, and representative examples include converter furnaces and AOD furnaces. In this method, crude molten stainless steel melted in an electric furnace is charged into a reaction vessel having a bottom blowing tuyere, and oxygen or a mixed gas of oxygen and argon is blown into the bottom tuyere to decarburize. On the other hand, recently, as disclosed in Japanese Unexamined Patent Publication No. 58-130216, a top blowing There is also a method of blowing a mixed gas of oxygen and argon or oxygen and nitrogen, and in Japanese Patent Publication No. 59-21367, there is a method of blowing oxygen and an inert gas under the bath surface of a chromium-containing steel bath to cause a decarburization reaction. At the same time, pure oxygen or an oxygen-containing gas containing oxygen is blown onto the bath surface.
A method is also disclosed. The above method requires that oxygen for decarburization be injected through the bottom tuyeres of the furnace. This hearth bottom tuyere usually has a double pipe structure, and the AOD
In the furnace, a mixed gas of argon and oxygen is supplied from the inner tube, argon is supplied from the gap between the inner tube and the outer tube, and in the case of a bottom blowing converter, hydrocarbon gas is supplied from the gap between the inner tube and the outer tube. (Problems to be Solved by the Invention) In the conventional method described above, since oxygen is supplied from the bottom tuyere, the tuyere receives heat from oxidation of the molten steel and reaches a high temperature, resulting in melting. For this reason, the life of the tuyere is a major factor in determining the life of the furnace body, which hinders productivity and increases the amount of refractories used. On the other hand, it is also possible to supply pure oxygen from a top-blown lance, but the above-mentioned "Steel Handbook" p709-711
As described in , Cr oxidation is large and a large amount of highly viscous slag is generated, so it is not practical and has not been developed into a process. Here, we present a method for achieving economical decarburization of stainless steel using simple equipment by overcoming the above-mentioned disadvantages caused by the lifespan of the furnace body due to tuyere melting without problems such as losses caused by Cr oxidation. This is the purpose of this invention. (Means for Solving the Problems) This invention relates to a decarburization refining method for crude molten stainless steel, in which a non-oxidizing gas is introduced below the bath surface of the molten stainless steel to stir the molten steel, and at the same time, a non-oxidizing gas is introduced below the bath surface. The key to solving the above problem is to spray a mixed gas of oxygen and non-oxidizing gas. Here, rather than keeping the ratio of non-oxidizing gas to oxygen in the mixed gas blown onto the bath surface constant, it should be increased (increasing the amount of non-oxidizing gas) as the carbon concentration in the molten steel decreases. is more desirable. According to this invention, the corrosion rate of the bottom tuyere is lower than in the conventional method, so the furnace life is extended, and Cr oxidation can be suppressed to the same level as the oxygen bottom blowing method, so it is a simple method with low equipment and operating costs. You can get an economical process. When carrying out this invention, a reaction vessel 1 as shown in FIG. 1 is suitable, and it is necessary to equip a normal top-blowing converter with equipment capable of bottom-blowing gas. In addition, from the top blow lance 2, there are piping systems 3 and 4 that can blow a mixed gas of oxygen and non-oxidizing gas.
It is desirable to provide a device that can control the flow rate of each gas, such as an automatic flow rate control valve. Note that the piping systems 5 and 6 were installed in order to carry out a comparative example to be described later, and are not necessary in the present invention. Describe the specific details of the operating method. First, crude molten stainless steel is charged into a top-bottom blowing converter having the above-mentioned functions. At this time, non-oxidizing gas is allowed to flow through the bottom tuyere. Next, a top blowing lance is inserted into the furnace to blow oxygen or a mixed gas of oxygen and non-oxidizing gas onto the bath surface. The gas supplied from the top blowing lance depends on the carbon concentration in the steel, but blowing is started with only oxygen, and when the carbon concentration has been decarburized to around 1%, it is switched to a mixed gas of oxygen and non-oxidizing gas. If the blowing is continued, the amount of non-oxidizing gas used can be reduced, which is advantageous. Since there is an appropriate range at which the gas type is switched depending on the oxygen supply rate and the molten steel temperature, the above carbon concentration of around 1% is only an approximate value. As the decarburization reaction progresses, it is practical to reduce the ratio of oxygen to non-oxidizing gas to create conditions that thermodynamically facilitate preferential decarburization. Indicated by The flow rate of the non-oxidizing gas supplied from the bottom tuyere during blowing may be constant, but in the high carbon concentration region where decarburization takes priority, it should be kept relatively small, so that the flow rate of the non-oxidizing gas supplied from the bottom tuyeres during blowing is relatively small. The total amount of non-oxidizing gas used can be reduced by supplying a large amount of non-oxidizing gas once the concentration is reached. Specifically, after the carbon concentration reaches the point where Cr begins to oxidize, the
It is desirable to supply 0.2 Nm 3 /min or more; if the amount of bottom-blown gas is less than this, oxidation of chromium tends to increase and is not economical. However, if it exceeds 1.0 Nm 3 /min per ton of molten steel, the effect of stirring will not change significantly and the amount of non-oxidizing gas used will increase, which is also not economical. Therefore, considering economic efficiency, 0.2 to 1.0Nm 3 /
min is appropriate. The auxiliary raw materials added before and during blowing are the same as in the conventional method, such as quicklime, dolomite, or a coolant. In addition, instead of so-called stainless crude molten steel,
It is also possible to charge hot metal that has been dephosphorized in advance and then introduce a chromium source such as ferrochrome or chromium-containing ore into the furnace, and such cases are also simply included in the expression of crude stainless steel. . Of course, the chromium oxide in the slag is removed after decarburization and refining.
Similar to the conventional method, reduction with a reducing agent such as Fe-Si and simultaneous desulfurization are performed. In the above explanation, the non-oxidizing gas may be any gas that does not oxidize the chromium content, but in consideration of economic efficiency and handling, it is recommended to use argon, nitrogen, hydrogen, hydrocarbon gas, etc. alone or in combination. Be realistic. It is also possible to use nitrogen for the first half of the blowing and argon for the second half. On the other hand, the non-oxidizing gas supplied from the top blowing lance may be the same or different from the bottom blowing non-oxidizing gas. (Function) In the method of the present invention, a non-oxidizing gas which solely controls the stirring of the steel bath is used below the bath surface of the crude molten stainless steel, so damage to the bottom tuyere and further damage to the bottom refractory is greatly reduced. few. On the other hand, since a mixed gas is blown onto the bath surface for the purpose of preferential decarburization, the amount of Cr loss is also the same as in the conventional method. (Example) Example 1 Using a top-bottom blowing converter as shown in FIG. 55−
Blowing was attempted in each case of Comparative Example 2, which is described in Japanese Patent No. 115914, in which a small amount of non-oxidizing gas was blown from the bottom blowing tuyere and only oxygen was blown from the top blowing lance. Crude stainless steel is SUS304 melted in an electric furnace.
Five tons of (18% Cr-8% Ni-2.5% C) was poured into a top-bottom blowing converter as shown in Figure 1. All non-oxidizing gases supplied were argon. In blowing using a mixed gas, the mixing ratio with oxygen was gradually changed according to the calculated carbon concentration in the molten steel, as shown in Table 1. Further, when carrying out the present invention, only argon from the top blowing lance was used in calculating the mixed gas ratio in Table 1, without taking into consideration argon for bottom blowing.
【表】
吹錬の条件と結果を第2表に示す。ステンレス
粗溶鋼の装入温度は1425〜1450℃の範囲であつ
た。また、スラグの塩基度調整用に生石灰を投入
し、CaO/SiO2比を約2.5にした。
同一炭素濃度でのクロム酸化量を比較して第2
図に示す。図より明らかなように、この発明によ
れば比較例2の上吹き純O2のみによる吹錬より
クロム酸化量は少なく、混合ガスの底吹き法と同
等である。また、これらの吹錬時の炉底羽口の溶
損量を第3図に比較して示す。この発明の場合
は、底吹き法の1/3〜1/4の溶損速度であり、炉寿
命は3〜4倍であると推定される。
第2表の最右欄は、脱炭後にFe−Siによる還
元脱硫処理を行つた時のFe−Si投入後の撹拌時
間と処理後のサルフアー濃度である。
この発明のように底吹きガス量が従来の底吹き
法の1/2〜1/5でも十分にクロム酸化物の還元が進
みそれゆえ脱硫が進行している。[Table] Table 2 shows the blowing conditions and results. The charging temperature of the crude molten stainless steel was in the range of 1425 to 1450°C. In addition, quicklime was added to adjust the basicity of the slag, and the CaO/SiO 2 ratio was adjusted to approximately 2.5. Comparing the amount of chromium oxidation at the same carbon concentration, the second
As shown in the figure. As is clear from the figure, according to the present invention, the amount of chromium oxidation is smaller than the blowing using only top-blown pure O 2 in Comparative Example 2, and is equivalent to the mixed gas bottom-blowing method. Furthermore, the amount of erosion of the bottom tuyeres during these blowing processes is shown in comparison in FIG. In the case of this invention, the erosion rate is 1/3 to 1/4 that of the bottom blowing method, and the furnace life is estimated to be 3 to 4 times longer. The rightmost column of Table 2 shows the stirring time after Fe-Si injection and the sulfur concentration after the treatment when reductive desulfurization treatment with Fe-Si was performed after decarburization. As in this invention, even when the amount of bottom-blown gas is 1/2 to 1/5 of that of the conventional bottom-blowing method, the reduction of chromium oxide is sufficiently advanced, and therefore the desulfurization is progressing.
【表】【table】
【表】
実施例 2
この発明に従う吹錬法により16%Crステンレ
ス鋼を溶製するに際し、りん濃度を0.020%まで
脱りんした溶銑を4トン装入し、上吹きランスか
ら純O2を吹き込みながらコークス塊を添加した。
コークスと同時に高炭素フエロクロムを少量ずつ
合計1.6トン添加し、16%Crのステンレス粗溶鋼
を溶製した。
この時の炭素濃度は3.9%であつた。
引続き純O2による脱炭吹錬を行い。炭素濃度
が2.5%になつた時点で第1表に従つて上吹きラ
ンスから混合ガスを吹き込み始めた。ただし、混
合ガス用及び底吹き用ともアルゴンの代わりに窒
素を用いた。
炭素濃度が0.25%になつた時点で、窒素からア
ルゴンにガスの変更を行い、引続き上吹き混合ガ
スの吹錬を継続した。
以上の吹錬の途中及び最後の溶鋼の成分、温度
を第3表に示す。この表より、脱りん溶銑を用い
た場合も、また非酸化性ガスとして窒素からアル
ゴンへと切替えて吹錬しても、この発明は従来の
底吹き法と同等のステンレス鋼を得ることができ
ることはあきらかである。なお、最終製品の窒素
濃度は210ppmであつた。[Table] Example 2 When melting 16% Cr stainless steel by the blowing method according to the present invention, 4 tons of hot metal whose phosphorus concentration had been dephosphorized to 0.020% was charged, and pure O 2 was blown from a top blowing lance. Coke lumps were added at the same time.
At the same time as coke, a total of 1.6 tons of high carbon ferrochrome was added in small amounts to produce 16% Cr stainless steel. The carbon concentration at this time was 3.9%. Continued decarburization blowing using pure O2 . When the carbon concentration reached 2.5%, blowing of the mixed gas from the top blowing lance was started according to Table 1. However, nitrogen was used instead of argon for both mixed gas and bottom blowing. When the carbon concentration reached 0.25%, the gas was changed from nitrogen to argon, and blowing with the top-blown mixed gas was continued. Table 3 shows the components and temperatures of the molten steel during and at the end of the above blowing process. From this table, it can be seen that this invention can produce stainless steel equivalent to the conventional bottom blowing method even when dephosphorized hot metal is used or when blowing is performed by switching from nitrogen to argon as the non-oxidizing gas. is obvious. Note that the nitrogen concentration of the final product was 210 ppm.
【表】
発明の効果
この発明は、従来のステンレス鋼精錬のための
AOD炉や底吹き転炉のように、炉底羽口から酸
素を吹込まなくてもよいので、以下のような効果
がある。
(1) 羽口溶損速度が小さく、炉寿命が長くなるの
で耐火物コストが大幅に削減でき、かつ炉の補
修間隔が長くなるので、溶鋼製造の生産性が向
上する。
(2) 設備が簡単であるので建設費や稼動費が少な
くてすみ経済的である。
以上、この発明はステンレス鋼の脱炭精錬につ
いて述べた来たが、クロムやマンガンなどのよう
な酸化されやすい元素を含む高合金鋼の脱炭精錬
にももちろん適用できる。[Table] Effects of the Invention The present invention provides a method for refining conventional stainless steel.
Unlike AOD furnaces and bottom-blowing converters, there is no need to blow oxygen through the bottom tuyeres, so there are the following effects. (1) Since the tuyere erosion rate is low and the furnace life is extended, the cost of refractories can be significantly reduced, and the furnace repair interval is lengthened, which improves the productivity of molten steel production. (2) Since the equipment is simple, construction costs and operating costs are low, making it economical. Although this invention has been described above for decarburization refining of stainless steel, it can of course also be applied to decarburization refining of high alloy steel containing easily oxidized elements such as chromium and manganese.
第1図はこの発明の優位性を示すために吹錬を
行つた転炉の模式図、第2図は、ステンレス鋼の
脱炭を行つた時の吹錬後の炭素濃度とクロムの酸
化クロスの関係図、第3図は、炉底羽口の溶損速
度を従来法と比較して示した図表である。
1……上底吹き転炉、2……上吹きランス、3
……上吹きアルゴン及び窒素用配管、4……上吹
き酸素用配管、5……底吹き酸素用配管、6……
底吹きアルゴン及び窒素用配管。
Figure 1 is a schematic diagram of a converter in which blowing was carried out to demonstrate the superiority of this invention. Figure 2 shows the carbon concentration and chromium oxidation cross-section after blowing when decarburizing stainless steel. FIG. 3 is a chart showing the melting rate of the bottom tuyere in comparison with the conventional method. 1...Top-bottom blowing converter, 2...Top-blowing lance, 3
...Piping for top-blown argon and nitrogen, 4... Piping for top-blowing oxygen, 5... Piping for bottom-blowing oxygen, 6...
Piping for bottom-blown argon and nitrogen.
Claims (1)
を撹拌すると同時に、浴面上へ酸素と非酸化性ガ
スの混合ガスを吹きつける ことを特徴とするステンレス鋼の溶製方法。 2 浴面上へ吹きつける混合ガス中の酸素に対す
る非酸化性ガスの割合を溶鋼中炭素濃度の低下に
従い増加する1記載の方法。[Claims] 1. When decarburizing crude molten stainless steel, a non-oxidizing gas is introduced below the bath surface of the molten steel to stir the molten steel, and at the same time, oxygen and non-oxidizing gas are mixed onto the bath surface. A stainless steel melting method characterized by blowing gas. 2. The method according to 1, wherein the ratio of non-oxidizing gas to oxygen in the mixed gas blown onto the bath surface is increased as the carbon concentration in the molten steel decreases.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26834985A JPS62130210A (en) | 1985-11-30 | 1985-11-30 | Production of stainless steel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26834985A JPS62130210A (en) | 1985-11-30 | 1985-11-30 | Production of stainless steel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62130210A JPS62130210A (en) | 1987-06-12 |
| JPH0154409B2 true JPH0154409B2 (en) | 1989-11-17 |
Family
ID=17457298
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP26834985A Granted JPS62130210A (en) | 1985-11-30 | 1985-11-30 | Production of stainless steel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62130210A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2674041B2 (en) * | 1987-09-17 | 1997-11-05 | 日本鋼管株式会社 | Manufacturing method of low nitrogen stainless steel |
| JP2751924B2 (en) * | 1987-09-17 | 1998-05-18 | 日本鋼管株式会社 | Manufacturing method of low nitrogen stainless steel |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3252790A (en) * | 1956-06-27 | 1966-05-24 | Union Carbide Corp | Preparation of metals and alloys |
| BE610265A (en) * | 1960-11-18 | |||
| JPS5217808A (en) * | 1975-07-31 | 1977-02-10 | Olympus Optical Co Ltd | Manufacturing method of magnetic head |
| JPS55115914A (en) * | 1979-02-28 | 1980-09-06 | Sumitomo Metal Ind Ltd | Refining method of high chromium steel |
| JPS56142815A (en) * | 1980-04-07 | 1981-11-07 | Nisshin Steel Co Ltd | Refining method of stainless steel |
| JPS58130216A (en) * | 1982-01-28 | 1983-08-03 | Nippon Steel Corp | Refining method of high alloy steel and stainless steel |
| JPS5921367A (en) * | 1982-07-29 | 1984-02-03 | Satoshi Izawa | Apparatus for inducing vitamin d in shiitake mushroom |
-
1985
- 1985-11-30 JP JP26834985A patent/JPS62130210A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62130210A (en) | 1987-06-12 |
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