JP2855333B2 - Modification method of molten steel slag - Google Patents

Modification method of molten steel slag

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Publication number
JP2855333B2
JP2855333B2 JP1013447A JP1344789A JP2855333B2 JP 2855333 B2 JP2855333 B2 JP 2855333B2 JP 1013447 A JP1013447 A JP 1013447A JP 1344789 A JP1344789 A JP 1344789A JP 2855333 B2 JP2855333 B2 JP 2855333B2
Authority
JP
Japan
Prior art keywords
slag
molten steel
amount
ladle
reforming
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 - Lifetime
Application number
JP1013447A
Other languages
Japanese (ja)
Other versions
JPH02194113A (en
Inventor
義明 原
章一 日和佐
徳浩 永村
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Steel Corp
Original Assignee
Kawasaki Steel Corp
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Filing date
Publication date
Application filed by Kawasaki Steel Corp filed Critical Kawasaki Steel Corp
Priority to JP1013447A priority Critical patent/JP2855333B2/en
Publication of JPH02194113A publication Critical patent/JPH02194113A/en
Application granted granted Critical
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Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は溶鋼スラグの改質方法に係り、特に転炉等の
精錬炉で溶製した溶鋼を取鍋に出鋼し、取鍋内でスラグ
改質した後、真空脱ガス処理の2次精錬する高清浄度鋼
の溶製工程におけるスラグ改質方法に関し、酸素等の含
有ガスおよび非金属介在物のきわめて少ない高清浄度鋼
溶製分野で利用される。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for reforming molten steel slag, and in particular, taps molten steel smelted in a refining furnace such as a converter into a ladle. The slag reforming method in the slag reforming process of the high cleanliness steel subjected to the secondary refining of the vacuum degassing after the slag reforming is applied. Used in

〔従来の技術〕[Conventional technology]

近年、高清浄度鋼に対する要求が益々高まりつつある
が、高清浄度鋼は一般に溶鋼のRH、DH等の真空処理によ
る2次精錬で製造されている。
In recent years, demands for high cleanliness steel are increasing, and high cleanliness steel is generally manufactured by secondary refining by vacuum treatment of molten steel such as RH and DH.

このRH、DH等の真空処理は脱ガス及び介在物浮上促進
に極めて効果的であるが、スラグ中に多量に存在してい
るFeO、MnO等の酸化物が、RH、DH等の真空処理後に、溶
鋼中のAl等と反応して微小介在物を生成し鋼中に存在す
る問題がある。すなわち、転炉出鋼中に取鍋へ流出する
スラグはFeO、MnO濃度の高い酸化性スラグであり、これ
が鋳造までの間に鋼中のAlと反応してAl2O3を生成す
る。このAl2O3が非金属介在物として鋼中に残存し製品
の品質に悪影響を及ぼすものである。
This vacuum treatment of RH, DH, etc. is extremely effective in degassing and promoting the floating of inclusions, but oxides such as FeO, MnO, which are present in large amounts in the slag, are subjected to vacuum treatment of RH, DH, etc. In addition, there is a problem that it reacts with Al and the like in molten steel to form minute inclusions and exists in steel. That is, the slag flowing into the ladle during tapping of the converter is an oxidizing slag having a high concentration of FeO and MnO, which reacts with Al in the steel before casting to form Al 2 O 3 . This Al 2 O 3 remains in the steel as nonmetallic inclusions and adversely affects the quality of the product.

従つて、高清浄度鋼の溶製には、出鋼中に取鍋に流出
するスラグ(以下取鍋スラグと称する)を無害化するス
ラグ改質が必要である。
Therefore, slag reforming that renders slag flowing into a ladle (hereinafter referred to as a ladle slag) harmless during tapping is required for smelting high-cleanliness steel.

取鍋スラグの改質方法として、従来多くの研究が開示
されているが、特開昭59−70710では、製鋼炉からの出
鋼時に製品としてほぼ必要量の脱酸剤を添加すると共
に、脱酸生成物の合体浮上促進のためフラツクスを添加
する方法、もしくは更に酸化性スラグを改質するための
スラグ還元剤を併用添加する方法である。また、特開昭
60−152611では、スラグ還元剤と共にガス発生物質を併
用添加して、スラグを撹拌する方法が提示されている。
Although many studies have been disclosed in the past as a method of ladle slag reforming, Japanese Patent Application Laid-Open No. Sho 59-70710 discloses a method of adding almost a necessary amount of a deoxidizing agent as a product at the time of tapping from a steelmaking furnace, and This is a method in which a flux is added to promote the combined floating of the acid products, or a method in which a slag reducing agent for further modifying the oxidizable slag is added. In addition,
60-152611 discloses a method in which a gas generating substance is added together with a slag reducing agent to stir the slag.

しかし、これらの方法で取鍋スラグを還元すると、Fe
O、MnOのみならず、スラグ中に含まれているP2O5、SiO2
までも還元され、鋼中に有害元素であるP、Si濃度が上
昇するという問題が生ずる。
However, when ladle slag is reduced by these methods, Fe
Not only O and MnO but also P 2 O 5 and SiO 2 contained in slag
To reduce the concentration of P and Si, which are harmful elements, in steel.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

本発明の目的は、上記取鍋スラグの改質に係る従来技
術の欠点を解消し、P、Si等の有害元素のピツクアツプ
を抑制しながらFeO、MnO等を還元することができる効果
的な溶鋼スラグの改質方法を提供しようとするものであ
る。
An object of the present invention is to solve the drawbacks of the prior art relating to the reforming of ladle slag, and to reduce the amount of harmful elements such as P and Si while suppressing FeO, MnO and the like. An object of the present invention is to provide a method for reforming slag.

〔問題点を解決するための手段および作用〕[Means and actions for solving the problems]

本発明の要旨とするところは次の如くである。すなわ
ち、転炉にて吹錬し取鍋内に出鋼した溶鋼上に浮遊する
酸化性スラグを改質する溶鋼スラグの改質方法におい
て、前記転炉吹錬に際しP濃度0.030重量%以下の溶銑
を用いて吹止めスラグの塩基度を5.5以上とする吹錬を
行う工程と、前記転炉からの出鋼後取鍋内に流出したス
ラグ上に金属Alもしくは金属Alを含む還元剤を添加する
工程と、を有して成ることを特徴とする溶鋼スラグの改
質方法である。
The gist of the present invention is as follows. That is, in a method of reforming molten steel slag which reforms oxidizing slag floating on molten steel blown in a converter and tapped into a ladle, the molten iron having a P concentration of 0.030% by weight or less in the converter blowing. And a step of performing blowing with the basicity of the blow-stop slag to 5.5 or more, and adding a metal Al or a reducing agent containing metal Al onto the slag flowing into the ladle after tapping from the converter. And a process for modifying molten steel slag.

本発明の詳細を添付図面を参照して説明する。取鍋ス
ラグの改質に当り、転炉装入前の溶銑中のP濃度を低く
すると、吹錬中に必要な脱P量が減少するため、スラグ
中に移行するP量も減少する。従つて本発明者らは、こ
れによりスラグ還元を行つた場合のスラグから溶鋼への
Pのピツクアツプを抑へることができると考え、P濃度
の種々異なる溶銑を用い、転炉にて吹錬した後、スラグ
還元を行い、スラグ還元時の復P量を調査した。結果は
第1図に示すとおりである。第1図に示した実験は、そ
れぞれ溶銑中のP濃度が重量比にて0.02%、0.04%、0.
06%、0.08%の溶銑を吹錬し、取鍋内に出鋼した溶鋼上
のスラグに、還元剤として同量の1kg/溶鋼tの金属Alに
てスラグ還元した時の鋼中への復りん量を調査したもの
である。
The details of the present invention will be described with reference to the accompanying drawings. In reforming the ladle slag, if the P concentration in the hot metal before charging the converter is reduced, the amount of P removed during blowing decreases, so the amount of P transferred into the slag also decreases. Therefore, the present inventors consider that it is possible to suppress the pick-up of P from the slag to the molten steel when slag is reduced by this, and to blow the molten iron in the converter using hot metal having various P concentrations. After that, slag reduction was performed, and the amount of return P at the time of slag reduction was investigated. The results are as shown in FIG. In the experiment shown in FIG. 1, the P concentrations in the hot metal were 0.02%, 0.04%, and 0.
06% and 0.08% of hot metal is blown and returned to the steel when the slag is reduced to the slag on the molten steel by tapping into the ladle with the same amount of metallic Al as 1kg / t as a reducing agent. It is a survey of phosphorus content.

第1図から明らかな如く、転炉吹錬に使用する溶銑の
P濃度を0.030%以下にすることにより、鋼中への復り
ん量を操業上および鋼品質上差支えないPレベルである
0.002%以下にできることが判明した。従つて本発明で
は、転炉吹錬に際しPの濃度0.030重量%以下の予備処
理溶銑を使用することに限定した。
As is clear from FIG. 1, the P concentration of the hot metal used for converter blowing is 0.030% or less, so that the amount of rephosphorized iron in the steel is a P level that does not affect the operation and the steel quality.
It turned out that it can be less than 0.002%. Therefore, in the present invention, the use of pretreated hot metal having a P concentration of 0.030% by weight or less in the converter blowing is limited.

次にP濃度の低い溶銑を使用して転炉で吹錬すると、
吹錬中の脱りん量が小さくてよいため、スラグの塩基度
CaO/SiO2を高くして、滓化性が悪くなつても特に操業上
問題が生じないと考えられたので、スラグの塩基度を高
くしてスラグ還元時のSiのピツクアツプ量を減少させる
試験操業を行つた。すなわち、吹止スラグの塩基度CaO/
SiO2を3〜8と種々変化して吹錬した溶鋼について、取
鍋スラグの改質に際し、それぞれ先の試験と同様に、い
ずれもスラグ還元剤として1kg/溶鋼tの金属Alを使用し
た時の、溶鋼へのSiのピツクアツプ量を調査した。結果
は第2図に示すとおりである。第2図から明らかな如
く、転炉の吹上スラグの塩基度を5.5以上とすることに
より、取鍋スラグの改質還元時の溶鋼中へのSiのピツク
アツプ量を0.01%以下にすることができることが判明し
た。従つて、本発明では、転炉吹上めスラグの塩基度Ca
O/SiO2を5.5以上とする吹錬を行うことに限定した。
Next, when the hot metal with low P concentration is blown in a converter,
Since the amount of dephosphorization during blowing can be small, the basicity of slag
It was thought that there would be no particular problem in operation even if CaO / SiO 2 was increased and the slagging property deteriorated, so a test to increase the basicity of slag and reduce the amount of Si pickup during slag reduction. Went into operation. That is, the basicity CaO /
In the case of ladle slag reforming for molten steel blown with various changes of SiO 2 from 3 to 8, as in the previous test, when using 1 kg / metal Al of molten steel t as a slag reducing agent in each case The amount of Si picked up in molten steel was investigated. The results are as shown in FIG. As is clear from FIG. 2, by setting the basicity of the blow-up slag of the converter to 5.5 or more, the amount of Si pick-up in the molten steel during the reforming reduction of the ladle slag can be made 0.01% or less. There was found. Therefore, in the present invention, the basicity Ca of the converter blow-up slag
It was limited to blowing with O / SiO 2 of 5.5 or more.

なお、上記Siのピツクアツプ量が0.01%以下は操業上
および鋼品質上全く問題が生じない範囲であり、また吹
上スラグの塩基度CaO/SiO2を5.5以上としても、吹止め
P濃度については、なんら問題が生じないことを確認し
た。
The Si pick-up amount of 0.01% or less is within a range where no problem occurs in operation and steel quality at all, and even when the basicity CaO / SiO 2 of the blow-up slag is 5.5 or more, the blow-off P concentration is as follows. Confirmed that no problem occurred.

また、本発明により吹止スラグの塩基度を5.5以上と
した場合には、スラグの溶融点が高く、出鋼時に一部は
固化して炉内に残るため、取鍋へ流出するスラグ量が第
3図に示す如く、塩基度CaO/SiO2の上昇と共に次第に少
くなり、塩基度が5.5以上の場合の流出スラグ量は3kg/
溶鋼t以下となる。
Further, when the basicity of the blow stop slag is set to 5.5 or more according to the present invention, the melting point of the slag is high, and part of the slag solidifies during tapping and remains in the furnace, so that the amount of slag flowing out to the ladle is reduced. third, as shown in FIG gradually becomes less with increasing basicity CaO / SiO 2, the outflow amount of slag in the case basicity of 5.5 or more is 3 kg /
It is less than molten steel t.

本発明者らは、塩基度の差による流出スラグ量(kg/
溶鋼t)の変化に対するスラグ還元時の復りん量(%)
について調査した。結果は第4図に示すとおりである。
第4図から明らかな如く、流出スラグ量が少なければ当
然復りん量も少なくなり、流出スラグ量が塩基度5.5以
上によつて3kg/溶鋼t以下と少くなれば、復りん量が0.
002%以下と少くなる副次的効果もあることが判明し
た。
The present inventors have found that the amount of slag effluent (kg /
Phosphorus recovery during slag reduction with respect to change in molten steel t) (%)
Was investigated. The results are as shown in FIG.
As is clear from FIG. 4, if the amount of effluent slag is small, the amount of rephosphorus will naturally be small.
It was also found that there was a secondary effect that was less than 002%.

〔実施例〕〔Example〕

P:0.025重量%の予備処理溶銑を使用し、吹止スラグ
の塩基度CaO/SiO2=6.5にて転炉で吹錬した溶鋼の取鍋
スラグにスラグ還元剤として1kg/溶鋼tの金属Alを添加
して本発明によるスラグ改質を実施し、併せてP:0.060
重量%および0.062重量%の溶銑を使用し、吹止スラグ
の塩基度をそれぞれ4.5および6.3とした溶鋼を出鋼した
比較例1および比較例2、ならびに、P:0.023重量%の
予備処理溶銑を使用し、吹止スラグの塩基度CaO/SiO2
4.6の比較例3について、いずれも溶鋼にスラグ還元剤
として同量の1kg/溶鋼tの金属Alを添加する同一法によ
るスラグ還元を行い、その結果を比較する比較試験を行
つた。結果は第1表に示す通りである。
P: 0.025% by weight of pre-treated hot metal, with the basicity of the blow-off slag CaO / SiO 2 = 6.5. To perform slag reforming according to the present invention, together with P: 0.060
Comparative Example 1 and Comparative Example 2 in which molten steel with a basicity of 4.5 g and 6.3 in the blow stop slag was used, respectively, using hot metal of 0.062 weight% and 0.062 weight%, and P: 0.023 weight% of pretreated hot metal Used, basicity of blow slag CaO / SiO 2 =
Regarding Comparative Example 3 of 4.6, slag reduction was performed by the same method in which the same amount of metal Al of 1 kg / t was added to molten steel as a slag reducing agent, and a comparative test was performed to compare the results. The results are as shown in Table 1.

第1表より明らかな如く、比較例1では転炉吹錬に使
用した溶銑のP濃度が高いために復りん量が0.005%と
高く、かつ吹止スラグの塩基度が4.5と低いためにSiの
ピツクアツプ量が0.03%と高くなっている。更に転炉か
らのスラグ流出量が多いために改質処理後のT.Feが4.5
%と高い。
As is clear from Table 1, in Comparative Example 1, since the P concentration of the hot metal used in the converter blowing was high, the rephosphorization amount was as high as 0.005%, and the basicity of the blowoff slag was as low as 4.5. Pick-up amount is as high as 0.03%. Furthermore, since the amount of slag flowing out of the converter is large, T.Fe after the reforming treatment is 4.5
% And high.

また比較例2においては、吹止スラグの塩基度が本発
明の要件に合致しているのでΔ〔%Si〕が0.01%以下と
低く、かつスラグ量が少いために改質処理後のT.Feが3.
2と低いものの、使用溶銑のP濃度が0.062%と高いため
にΔ〔%P〕が高くなっている。
In Comparative Example 2, since the basicity of the blow stop slag met the requirements of the present invention, Δ [% Si] was as low as 0.01% or less, and the slag amount was small. Fe is 3.
Although it is as low as 2, Δ [% P] is high because the P concentration of the hot metal used is as high as 0.062%.

また比較例3では、吹止スラグの塩基度が4.6と低い
ためにΔ〔%Si〕が高く、かつ転炉からのスラグ流出量
が多いために、使用溶銑のP濃度が低いにも拘らずΔ
〔%P〕が高くなつている。
In Comparative Example 3, Δ [% Si] was high due to the low basicity of blow slag being 4.6, and the slag outflow from the converter was large. Δ
[% P] is increasing.

一方、本発明による要件をすべて満足する本発明例
は、上記各比較例と同一量のスラグ還元剤を使用してい
るに拘らず、Δ〔%P〕=0.001%、Δ〔%Si〕=0.01
%以下となり、P、Siのピツクアツプ量がきわめて低く
抑えられていることがわかる。上記各比較例から明らか
な如く、本発明のいずれかの要件を満足しても、他のす
べての要件を満足しないかぎり、Δ〔%P〕Δ〔%Si〕
ならびに改質処理後のT.Fe%のいずれかにおいて、満足
すべき値が得られない。換言すれば本発明によるすべて
の要件を満足する改質方法をとることにより常に酸化物
が少く、P、Si等の有害元素のピツクアツプを抑えて効
果的な取鍋スラグの改質が可能であることが判明した。
On the other hand, Examples of the present invention satisfying all the requirements according to the present invention have Δ [% P] = 0.001% and Δ [% Si] = 0.01
% Or less, indicating that the pickup amounts of P and Si are kept extremely low. As is clear from each of the above comparative examples, even if one of the requirements of the present invention is satisfied, Δ [% P] Δ [% Si] unless all other requirements are satisfied.
In addition, a satisfactory value cannot be obtained in any of the T.Fe% after the modification treatment. In other words, the reforming method that satisfies all the requirements according to the present invention always has a small amount of oxides, suppresses the pickup of harmful elements such as P and Si, and enables effective reforming of ladle slag. It has been found.

〔発明の効果〕〔The invention's effect〕

本発明は上記実施例から明らかな如く、従来の取鍋ス
ラグの改質方法では、FeO、MnOが還元されるのみなら
ず、有害元素のP、Siまでも還元される欠点に鑑み、本
発明は、転炉吹錬に際しP濃度が0.030重量%以下の予
備処理溶銑を使用し、かつ吹止めスラグの塩基度CaO/Si
O2を5.5以上とする吹錬を行つた上で、取鍋スラグ上に
金属Alもしくは金属Alを含む還元剤を添加する方法をと
つたので、次の効果を挙げることができた。
As is apparent from the above-described embodiment, the present invention has been made in view of the disadvantage that not only FeO and MnO are reduced but also harmful elements P and Si are reduced by the conventional ladle slag reforming method. Uses pretreated hot metal with a P concentration of 0.030% by weight or less in converter blowing and basicity of blow-off slag CaO / Si
Since the method of adding metal Al or a reducing agent containing metal Al to the ladle slag after performing blowing with O 2 of 5.5 or more was adopted, the following effects were obtained.

(イ)取鍋スラグの改質時のP、Si等の有害元素のピツ
クアツプ量を最小限に抑えることができる。
(B) The amount of pick-up of harmful elements such as P and Si during ladle slag reforming can be minimized.

(ロ)取鍋スラグ中のT.Fe等を低減することができ、鋼
中のAlとスラグ中のFeO、MnOとの反応によるAl2O3の生
成量が少くなり、鋼品質の悪化をもたらす非金属介在物
量を低減することができた。
(B) T.Fe etc. in ladle slag can be reduced, and the amount of Al 2 O 3 produced by the reaction between Al in steel and FeO and MnO in slag decreases, resulting in deterioration of steel quality. The resulting non-metallic inclusions could be reduced.

【図面の簡単な説明】[Brief description of the drawings]

第1図は本発明を得る実験における転炉吹錬に使用する
溶銑のP濃度の取鍋スラグ改質時の復りん量に及ぼす影
響を示す線図、第2図は転炉吹止スラグの塩基度CaO/Si
O2の取鍋スラグ改質時のSiピツクアツプ量(%)に及ぼ
す影響を示す線図、第3図は吹止スラグの塩基度の転炉
より流出するスラグ量(kg/溶鋼t)に及ぼす影響を示
す線図、第4図は転炉流出スラグ量(kg/溶鋼t)の取
鍋スラグ改質時の復りん量に及ぼす影響を示す線図であ
る。
FIG. 1 is a diagram showing the effect of the P concentration of the hot metal used for converter blowing in the experiment for obtaining the present invention on the rephosphorization amount during ladle slag reforming, and FIG. Basicity CaO / Si
Diagram showing the effect of O 2 on the amount of Si pick-up (%) during ladle slag reforming. FIG. 4 is a graph showing the effect of the amount of slag (kg / t of molten steel) flowing out of the converter on the amount of reconstituted phosphorus at the time of ladle slag reforming.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭63−169320(JP,A) 特開 昭51−12321(JP,A) 特開 昭55−76013(JP,A) (58)調査した分野(Int.Cl.6,DB名) C21C 7/00 F27D 15/00──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-63-169320 (JP, A) JP-A-51-12321 (JP, A) JP-A-55-76013 (JP, A) (58) Field (Int. Cl. 6 , DB name) C21C 7/00 F27D 15/00

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】転炉にて吹錬し取鍋内に出鋼した溶鋼上に
浮遊する酸化性スラグを改質する溶鋼スラグの改質方法
において、前記転炉吹錬に際しP濃度0.030重量%以下
の溶銑を用いて吹止めスラグの塩基度を5.5以上とする
吹錬を行う工程と、前記転炉からの出鋼後取鍋内に流出
したスラグ上に金属Alもしくは金属Alを含む還元剤を添
加する工程と、を有して成ることを特徴とする溶鋼スラ
グの改質方法。
1. A method of reforming molten steel slag for reforming oxidized slag floating on molten steel blown in a converter and discharged into a ladle, wherein a P concentration of 0.030% by weight is used in the converter blowing. A step of performing blowing with the basicity of the blow-stop slag of 5.5 or more using the following hot metal, and a reducing agent containing metal Al or metal Al on the slag flowing into the ladle after tapping from the converter. And a step of adding slag.
JP1013447A 1989-01-23 1989-01-23 Modification method of molten steel slag Expired - Lifetime JP2855333B2 (en)

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JP1013447A JP2855333B2 (en) 1989-01-23 1989-01-23 Modification method of molten steel slag

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Application Number Priority Date Filing Date Title
JP1013447A JP2855333B2 (en) 1989-01-23 1989-01-23 Modification method of molten steel slag

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JPH02194113A JPH02194113A (en) 1990-07-31
JP2855333B2 true JP2855333B2 (en) 1999-02-10

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102828040A (en) * 2012-09-25 2012-12-19 鞍钢股份有限公司 Method for recycling metallic aluminium in pre-melted slag of vacuum circulation degassing furnace

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5112321A (en) * 1974-07-23 1976-01-30 Nippon Steel Corp Teisansokono seizohoho
JPS5576013A (en) * 1978-12-05 1980-06-07 Kobe Steel Ltd Al adding method to molten steel
JPS63169320A (en) * 1986-12-29 1988-07-13 Nippon Steel Corp Production of low-sulfur steel

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102828040A (en) * 2012-09-25 2012-12-19 鞍钢股份有限公司 Method for recycling metallic aluminium in pre-melted slag of vacuum circulation degassing furnace
CN102828040B (en) * 2012-09-25 2014-10-08 鞍钢股份有限公司 Method for recycling metallic aluminium in pre-melted slag of vacuum circulation degassing furnace

Also Published As

Publication number Publication date
JPH02194113A (en) 1990-07-31

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