JPH02111810A - Method for preventing flowing-out of slag in converter - Google Patents

Method for preventing flowing-out of slag in converter

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Publication number
JPH02111810A
JPH02111810A JP26564788A JP26564788A JPH02111810A JP H02111810 A JPH02111810 A JP H02111810A JP 26564788 A JP26564788 A JP 26564788A JP 26564788 A JP26564788 A JP 26564788A JP H02111810 A JPH02111810 A JP H02111810A
Authority
JP
Japan
Prior art keywords
slag
mgo
converter
cao
blowing
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.)
Granted
Application number
JP26564788A
Other languages
Japanese (ja)
Other versions
JP2635721B2 (en
Inventor
Hideaki Yamamura
英明 山村
Hideyuki Misumi
三隅 秀幸
Toshiyuki Kaneko
敏行 金子
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.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
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Publication date
Application filed by Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP26564788A priority Critical patent/JP2635721B2/en
Publication of JPH02111810A publication Critical patent/JPH02111810A/en
Application granted granted Critical
Publication of JP2635721B2 publication Critical patent/JP2635721B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To prevent flowing-out of slag accompanied with molten steel at the time of tapping the molten steel by adding MgO so that solid phase ratio of the slag in a converter at the end period of blowing comes to the specific value in the blowing of molten iron. CONSTITUTION:At the time of blowing the molten iron, the MgO is added into the converter so that the solid phase ratio of the slag in the converter at the end period of the blowing or after completing the blowing comes to <=30%, to solidify the slag. In this purpose, in accordance with CaO/SiO2 and T.Fe content in the slag in the converter, the MgO is added so as to come to MgO (%)>=[T.Fe(%)+39.3]/2.1 in the case of 3<=CaO/SiO2<4, MgO(%)>=[T.Fe (%)+4.4]/0.8 in the case of 4<=CaO/SiO2<5 and MgO(%)>=[T.Fe(%)-4.2]/0.7 in the case of 5<=CaO/SiO2<6. By this method, the flowed-out slag quantity at the time of tapping the molten steel is reduced to <= about 6kg/ton.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は/8@出鋼前に転炉内スラグを固化して出鋼時
にl8鋼に随伴して転炉内スラグが流出するのを防止す
る方法に関するものである。
[Detailed description of the invention] <Industrial application field> The present invention solidifies the slag in the converter before /8@ steel tapping to prevent the slag in the converter from flowing out along with l8 steel during tapping. It is about how to prevent it.

〈従来の技術〉 転炉内スラグが出鋼時に溶鋼と共に流出するとそれ自体
が介在物となる上に、脱酸後の溶鋼酸化源となり、溶鋼
の清浄度が低下する。
<Prior Art> When the slag in the converter flows out together with the molten steel during tapping, it not only becomes inclusions but also becomes a source of oxidation of the molten steel after deoxidation, reducing the cleanliness of the molten steel.

このため従来は、特願昭62−192136号に提案さ
れている様に、スラグのT、Fe量に応じてCaOを添
加してスラグの塩基度Can /SiO□を劇整し、該
スラグを固化し、上記した出鋼時の流出を防止して出鋼
する方法を採っていた。
For this reason, conventionally, as proposed in Japanese Patent Application No. 1982-192, CaO was added according to the T and Fe contents of the slag to drastically adjust the basicity of the slag, Can/SiO□, and the slag was The method used was to solidify the steel and prevent it from flowing out during tapping as described above.

この方法は第3図に示す如き、転炉内スラグ中のT、F
eと該スラグの塩基度CaO/Singの関係を基に行
われている。
This method is as shown in Fig. 3.
This is based on the relationship between e and the basicity of the slag, CaO/Sing.

図中の破線は過去の実績から得た固化成否境界線で、こ
の線から右下の範囲が固化が成功する領域とされている
The broken line in the figure is the solidification success/failure boundary line obtained from past results, and the range to the lower right of this line is considered to be the area where solidification is successful.

しかしながら固化はT、Fe以外のスラグの組成によっ
ても条件が異なり、同−T、Feでもスラグの融点を下
げるAh03等の濃度が高くなると、スラグ固化に必要
な塩基度は高くなり、これによってCaOは益々多量を
必要とし、その結果転炉内のスラグ量は増大する。
However, the conditions for solidification differ depending on the composition of the slag other than T and Fe, and even with T and Fe, if the concentration of Ah03, etc., which lowers the melting point of the slag, increases, the basicity required for slag solidification increases, which causes CaO As a result, the amount of slag in the converter increases.

この問題を解決するものとして特開昭63〜79910
号公報の提案がある。
To solve this problem, Japanese Patent Application Laid-Open No. 63-79910
There is a proposal for a publication.

この提案はそれ自体周知である現象を用いたもので、M
gO自体が高融点酸化物であってCaO−5iOFen
系スラグにMgOを一定限度以上添加すると上記スラグ
も高融点化する事を利用して転炉の精錬末期又は終了直
後に炉内にMgOを投入もしくは吹込んで転炉内スラグ
を高融点化して出鋼時の流出を最小に抑えるもので、炉
内スラグに加えるMgO量を該スラグ内のCaO重量の
0.3〜0.8重量比とするものである。
This proposal uses a well-known phenomenon, and M
gO itself is a high melting point oxide, CaO-5iOFen
When MgO is added to the system slag above a certain limit, the slag also has a high melting point. Taking advantage of this fact, MgO is introduced or blown into the converter at the end of refining or immediately after the refining of the converter to make the slag in the converter have a high melting point and then taken out. This is to minimize the outflow during steel production, and the amount of MgO added to the slag in the furnace is set at a weight ratio of 0.3 to 0.8 of the weight of CaO in the slag.

〈発明が解決しようとする課題〉 上記した従来のスラグ固化方法によると、スラグ固化が
安定しない事、これを安定して固化するには多量のCa
Oを必要とする事、その結果スラグ量が増大してスラグ
処理費が増大すると共に、冒頭に述べた目的の達成が困
難になる。これ等の問題を解決するために特開昭63−
79910号公報の提案を用いても■T、Feが高い場
合及び■SiO□が高い場合(CaO/Singが低い
時)はMgO/CaOが0.8でも炉内スラグは固化し
ない事がある。
<Problems to be solved by the invention> According to the conventional slag solidification method described above, the slag solidification is not stable, and a large amount of Ca is required to stably solidify the slag.
The need for O as a result increases the amount of slag, increases the slag processing cost, and makes it difficult to achieve the objectives stated at the beginning. In order to solve these problems, JP-A-63-
Even if the proposal of Publication No. 79910 is used, when ■T and Fe are high and when ■SiO□ is high (when CaO/Sing is low), the slag in the furnace may not solidify even if MgO/CaO is 0.8.

又実施例に記載されているMgO/CaOが0.36の
時にT、Feが高く、Can/SiO□が低い時には炉
内スラグが固化しない事があり、炉内スラグの固化が安
定しない事がある。この不安定な固化を安定させるには
出来るだけMgO/CaO□を高くする事が必要となる
。このためT、Feが低い場合や、或いはCan/Si
O□が高い場合には、それ以下でも固化するので余分な
MgOを使う事になり処理コストが増大する。
Furthermore, when MgO/CaO is 0.36 as described in the examples, when T and Fe are high and Can/SiO□ is low, the furnace slag may not solidify, and the solidification of the furnace slag may not be stable. be. In order to stabilize this unstable solidification, it is necessary to increase MgO/CaO□ as much as possible. Therefore, when T and Fe are low, or when Can/Si
If O□ is high, solidification will occur even if it is less than that, so extra MgO will be used, increasing processing cost.

本発明はT、FeやCaO/ SiO2更にはA1.0
2が変化しても安定して転炉内スラグを固化すると共に
該炉内スラグの固化費を格段に低減する方法を提供する
事を課題とするものである。
The present invention uses T, Fe, CaO/SiO2, and A1.0
It is an object of the present invention to provide a method for stably solidifying slag in a converter even if 2 changes, and significantly reducing the cost of solidifying the slag in a converter.

〈課題を解決するための手段〉 本発明は上記課題を解決するために、 (1)溶銑の吹錬において、吹錬末期又は吹錬終了後に
転炉内スラグの固相率が30%以上となる星のMgOを
転炉内に添加するiJ(を基本的な手段とし、(2)溶
銑の吹錬において、吹諌末朋又は吹ilI終了後に、転
炉内スラグの[aO/SiO□及び1’、Fe量に応じ
てMgOを により転炉内に添加する事を具体的な手段とするもので
ある。
<Means for Solving the Problems> In order to solve the above problems, the present invention has the following objectives: (1) In blowing hot metal, the solid phase ratio of slag in the converter is 30% or more at the end of blowing or after the end of blowing. The basic method is to add MgO into the converter, and (2) in hot metal blowing, after the completion of blowing or blowing, [aO/SiO□ and 1', a specific method is to add MgO into the converter according to the amount of Fe.

く作用〉 本発明者等は上記課題の解決を目的として種々実験・検
討を繰り返した。
Effects> The present inventors have repeatedly conducted various experiments and studies with the aim of solving the above problems.

その結果、前記したそれぞれの従来技術は、転炉内スラ
グの融点に影古力がある該スラグ成分の中、T、Feと
CaO/5iOzにのみ、又はMgO/CaOにのみ着
目し、各々を別々に検討している事に問題がある事を見
出した。
As a result, each of the above-mentioned conventional technologies focuses only on T, Fe, and CaO/5iOz or only on MgO/CaO among the slag components that affect the melting point of the slag in the converter. I found that there is a problem with considering them separately.

本発明者等は実験・検討により、第4図に示す関係を得
た0図はスラグの固相率と取鍋内に流出したスラグ量の
関係を示したものである。
Through experiments and studies, the present inventors obtained the relationship shown in Figure 4. Figure 0 shows the relationship between the solid phase ratio of slag and the amount of slag flowing into the ladle.

ここでスラグの固相率とは、その反応点での各成分値(
サンプリング値)を基に広く当分野で用いられている方
法、例えば標(ゼ自由エネルギ生成の自由エネルギー、
活量係数等の熱力学データを用いて、反応点においてス
ラグ中に生成した晶出物(固相)の割合を平衡計算によ
って求めた値を言う。
Here, the solid phase ratio of slag means the value of each component at the reaction point (
For example, a method widely used in this field is based on the sampled value).
This is the value determined by equilibrium calculation of the proportion of crystallized substances (solid phase) formed in the slag at the reaction point using thermodynamic data such as activity coefficients.

本発明者等は図により、転炉内スラグの固化はスラグの
固相率に基本的に支配されており、この固相率が30%
以上になると、スラグの融点に影響するスラグの成分が
変化しても出鋼時に流出するスラグ量が6kg/lon
以下と著しく減少し、実質的に前記課題の総てが解決出
来る事を見出した。
The present inventors have shown that the solidification of slag in the converter is basically controlled by the solid phase ratio of the slag, and this solid phase rate is 30%.
In this case, even if the slag components that affect the melting point of slag change, the amount of slag flowing out during tapping will be 6 kg/lon.
It has been found that substantially all of the above-mentioned problems can be solved.

次いで本発明者等は、スラグの固相率30%を確立する
に当たって、スラグのT、Fe 、 CaO/SiO□
に応して必要なスラグ固化剤の種類及び量について検討
を行った。この検討で本発明者等は第5図の関係を見出
した。
Next, in establishing a solid phase ratio of 30% in the slag, the present inventors determined that the slag's T, Fe, CaO/SiO□
We investigated the type and amount of slag solidifying agent required. Through this study, the inventors discovered the relationship shown in FIG.

CaOによる固化を前提とした場合、第5図に示す固化
限界を示すCan /SiO□と固化前人hOi含有量
との関係は、図に明らかな様にT、Feを一定にしても
一般的操業範囲に於いてはA1□03の含a量の変化に
応じて固化限界は大幅に変化した。
Assuming solidification by CaO, the relationship between Can /SiO□ showing the solidification limit and the pre-solidification hOi content shown in Figure 5 is general even if T and Fe are held constant, as is clear from the figure. Within the operating range, the solidification limit changed significantly as the a content of A1□03 changed.

そこでA1.o、の影ツの少ない固化剤につい”ζ調査
し、第2図に示す知見を得た。
So A1. We conducted an investigation on solidifying agents with less influence of o and ζ, and obtained the findings shown in Fig. 2.

図は該調査におけるスラグ中の^+2o323度と、ス
ラグ固化剤としてのMgoとCaOの各添加量の関係を
整理した結果を示す。
The figure shows the results of the investigation on the relationship between the temperature in the slag and the amounts of Mgo and CaO added as slag solidifying agents.

図から実線で示したMgOの添加量は、A1□03濃度
の影響が小さく、点線で示したCaOの添加量に対して
略70%で良い事が判明した。
It has been found from the figure that the amount of MgO added indicated by the solid line is less affected by the A1□03 concentration, and can be approximately 70% of the amount of CaO added indicated by the dotted line.

そこで更に検討を重ねた結果、MgOの必要添加量はC
aO/ 5411Kによって異なり、又転炉吹錬の一般
的範囲ではAI□034度の変化は1〜5%と小さ(、
MgOによる固化ではこの程度のA1□O1の変化では
固化に必要なMgO量の変化は実質的には生じない事か
ら一般的転炉吹錬では固化のためのMgO添加量はT、
FeとCaO/SiO□によって決まる事が判明した。
After further consideration, we found that the required amount of MgO to be added was C.
It varies depending on the aO/5411K, and in the general range of converter blowing, the change in AI□034 degrees is as small as 1 to 5% (,
In solidification with MgO, this degree of change in A1□O1 does not substantially change the amount of MgO required for solidification, so in general converter blowing, the amount of MgO added for solidification is T,
It was found that it is determined by Fe and CaO/SiO□.

第1図はその関係を示す。Figure 1 shows the relationship.

そこで第1図を基にCan /Sin□別にMgDの添
加量を転炉内スラグのT、Feとの関係から整理し、た
ものである。
Therefore, based on FIG. 1, the amount of MgD added for each Can/Sin□ was organized from the relationship with T and Fe of the slag in the converter.

〈実施例〉 以下に本発明例を比較例と共に示す。<Example> Examples of the present invention are shown below along with comparative examples.

(11使用転炉   上底吹き転炉(340ton/c
h)(2)転炉吹止温度 1600°C−1750℃(
3)吹止成分 (C)  :0.02〜0.50% (Mn)  : 0.2 〜2.0% <p3  :0.005〜0.030%[5)  :0
.001〜0.03% (4)スラグ成分 CaO: 35.0〜65.0% FeO:  7.0〜28.0% SiO□:5.0〜18.0% ’lnl]  :  2.0〜35.0%!4.<o 
 :  5.Q〜1O10%Alzc13:  t、0
〜5.0% (5)固化剤の添加方法。
(11 converters used: top-bottom blowing converter (340 ton/c)
h) (2) Converter blow-off temperature 1600°C-1750°C (
3) Blowing component (C): 0.02-0.50% (Mn): 0.2-2.0% <p3: 0.005-0.030% [5): 0
.. 001~0.03% (4) Slag component CaO: 35.0~65.0% FeO: 7.0~28.0% SiO□: 5.0~18.0% 'lnl]: 2.0~ 35.0%! 4. <o
: 5. Q~1O10%Alzc13: t, 0
~5.0% (5) Method of adding solidifying agent.

l8鋼のサンプルからl8鋼の凝固温度を検出し、これ
から溶鋼が含有する炭素Mを算出し、第6図に示す過去
の実績から求めた溶鋼の炭素含有量と”I’、Feの関
係図からT、Fl!を求め、CaO投人量と溶銑及び副
原料中のSi成分から計算される5iOz発生壇からC
aO7540gを予測し、この値に応してスラグの固相
率を30%以上にするのに必要なスラグ固化剤量を上記
関係式で求めて添加した。
The solidification temperature of l8 steel is detected from the sample of l8 steel, and the carbon M contained in the molten steel is calculated from this. Figure 6 shows the relationship between the carbon content of the molten steel determined from past results, "I", and Fe. Calculate T and Fl! from the 5iOz generation bed calculated from the amount of CaO input and the Si content in the hot metal and auxiliary raw materials.
7,540 g of aO was predicted, and in accordance with this value, the amount of slag solidifying agent required to make the solid phase ratio of slag 30% or more was calculated from the above relational expression and added.

上記T、FeやCan /SiO□を求めるには計算に
よる他、直接分析し検出する方法を用いても良い。
In order to obtain the above-mentioned T, Fe, and Can/SiO□, a method of direct analysis and detection may be used in addition to calculation.

処理条件と結果を比較例と共に第1表に示す。The processing conditions and results are shown in Table 1 along with comparative examples.

本発明実施例の試験番号1〜13では(1〜5は3≦C
aO7540g< 4 、 6〜9は4≦CaO/si
o、<5.10〜13は5≦Can / 5iOz <
 6の場合)、出鋼時の取鍋へのスラグ流出量は安定し
、MgO/Canが0.9の5及び0.2の8を含み6
kg/lon以下になった。
In test numbers 1 to 13 of the examples of the present invention (1 to 5 are 3≦C
aO7540g<4, 6-9 is 4≦CaO/si
o, <5.10-13 is 5≦Can/5iOz<
6), the amount of slag flowing into the ladle during tapping is stable, including 5 with MgO/Can of 0.9 and 8 with 0.2.
kg/lon or less.

これ等本発明例ではスラグ流出量が激減した結果、取鍋
へのAI添加時のA1歩留が60%以上の高位に安定し
、T、Oも25ρρl以下に安定して低くなった。尚M
gO源としてはMg0粒を用いても破砕したMgO煉瓦
を用いても同様の効果を得た。
In these examples of the present invention, as a result of the drastic reduction in the amount of slag flowing out, the A1 yield when adding AI to the ladle was stabilized at a high level of 60% or more, and T and O were also stably reduced to 25 ρρl or less. Nao M
Similar effects were obtained whether Mg0 grains or crushed MgO bricks were used as the gO source.

一方、Canを添加してスラグ固化を行った比較例の試
験番号14〜17に於いて15〜17はMgOの場合と
同様の効果を得たが、多量のスラグ固化剤を必要とした
。又14はT、FeとCaOの関係では固化する領域に
入っているが、Ah03が5%と高がったため流出スラ
グ量が増加した。
On the other hand, in test numbers 14 to 17 of comparative examples in which slag solidification was performed by adding Can, test numbers 15 to 17 obtained the same effect as in the case of MgO, but required a large amount of slag solidifying agent. Further, although No. 14 is in the solidification range in terms of the relationship between T, Fe, and CaO, the amount of slag flowing out increased because the Ah03 content was as high as 5%.

又、Mgflを添加しなかった比較例の19.2I、2
3及びMgOを添加したもののスラグ組成が固化領域に
入っていなかった比較例の18.20.22.24では
出鋼時の取鍋へのスラグ流出量が10kg/lon以上
に達し、その結果A1歩留は50%以下に低下し、7.
0は35ppm以上となりン容鋼の清浄度が低下した。
In addition, 19.2I, 2 of comparative example in which Mgfl was not added
In Comparative Example 18.20.22.24 in which the slag composition was not in the solidified region even though 3 and MgO were added, the amount of slag flowing into the ladle during tapping reached 10 kg/lon or more, and as a result, A1 7. Yield decreases to below 50%.
0 was 35 ppm or more, and the cleanliness of the container steel decreased.

又比較例の18.20.22.24はMgO/CaOが
0.3〜0.8の範囲にあったが戸内スラグは満足に固
化せず、流出スラグ量は10kg/Tを超えた。
Comparative example 18.20.22.24 had MgO/CaO in the range of 0.3 to 0.8, but the indoor slag was not solidified satisfactorily, and the amount of slag flowing out exceeded 10 kg/T.

〈発明の効果〉 本発明は、溶銑吹諌末期又は終了後に転炉内スラグのT
、Fe及びCaO/SiO□を求め、これを基にスラグ
固相率が30%以上になるスラグ固化剤として必要なM
gOlを添加するので従来のUaO又はMgOの添加に
よるスラグ固化に比して、a−要固化剤量が少なくなる
にもかかわらず、スラグ固化は安定して溶鋼取消に流出
するスラグ量は大幅に低減する。これにより合金歩留は
向上し、更に(g鋼の清浄度が格段に向上する等もたら
す効果は大きい。
<Effects of the Invention> The present invention improves the T of slag in the converter at the end of hot metal blowing or after completion
, Fe and CaO / SiO
Since gOl is added, compared to conventional slag solidification by adding UaO or MgO, although the amount of a-solidifying agent required is smaller, slag solidification is stable and the amount of slag flowing out to molten steel is significantly reduced. reduce As a result, the alloy yield is improved, and furthermore, the cleanliness of the (g) steel is greatly improved, and other effects are great.

【図面の簡単な説明】 第1図はスラグ固相率30%以上を達成するM、gO量
とCaO/SiO□星の関係を示し、第2図はスラグ固
相率30%以上を達成するMgOlとAlzOz It
の関係及びCaO量とA1□03量の関係を示し、第3
図はスラグのT、Feと塩基度の関係を示す。 第4図はスラグの固相率と取鍋への流出スラグ量の関係
を示し、第5図はスラグの吹止前A1□02量七塩基度
の関係を示し、第6図は吹止時炭素量とT、Feの関係
を示す図である。
[Brief explanation of the drawings] Figure 1 shows the relationship between M and gO amounts and CaO/SiO□ stars to achieve a slag solid fraction of 30% or more, and Figure 2 shows the relationship between the slag solid fraction and the slag solid fraction of 30% or more. MgOl and AlzOz It
and the relationship between the amount of CaO and the amount of A1□03, and the third
The figure shows the relationship between T, Fe and basicity of slag. Figure 4 shows the relationship between the solid fraction of slag and the amount of slag flowing into the ladle, Figure 5 shows the relationship between A1□02 amount and basicity of slag before blow-off, and Figure 6 shows the relationship between slag solidity and basicity before blow-off. It is a figure showing the relationship between carbon content, T, and Fe.

Claims (2)

【特許請求の範囲】[Claims] (1)溶銑の吹錬において、吹錬末期又は吹錬終了後に
、転炉内スラグの固相率が30%以上となる量のMgO
を転炉内に添加しスラグを固化する事を特徴とする転炉
内スラグの流出防止方法。
(1) In hot metal blowing, MgO in an amount such that the solid phase ratio of the slag in the converter is 30% or more at the end of blowing or after the end of blowing.
A method for preventing the outflow of slag in a converter, which is characterized by adding to the converter to solidify the slag.
(2)溶銑の吹錬において、吹錬末期又は吹錬終了後に
、転炉内スラグのCaO/SiO_2及びT.Fe量に
応して、 3≦CaO/SiO_2<4の時 MgO(%)≧(T.Fe(%)+39.3)/2.1
4≦CaO/SiO_2<5の時 MgO(%)≧(T.Fe(%)+4.4)/0.85
≦CaO/SiO_2<6の時 MgO(%)≧(T.Fe(%)−4.2)/0.7の
MgOを転炉内に添加しスラグを固化する事を特徴とす
る転炉内スラグの流出防止方法。
(2) In hot metal blowing, CaO/SiO_2 and T. Depending on the amount of Fe, when 3≦CaO/SiO_2<4, MgO (%) ≧ (T.Fe (%) + 39.3)/2.1
When 4≦CaO/SiO_2<5, MgO (%) ≧ (T.Fe (%) + 4.4)/0.85
Inside the converter, which is characterized in that when ≦CaO/SiO_2<6, MgO (%) ≧ (T.Fe (%) - 4.2)/0.7, MgO is added into the converter to solidify the slag. Method for preventing slag outflow.
JP26564788A 1988-10-20 1988-10-20 How to prevent slag from flowing out of the converter Expired - Lifetime JP2635721B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26564788A JP2635721B2 (en) 1988-10-20 1988-10-20 How to prevent slag from flowing out of the converter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26564788A JP2635721B2 (en) 1988-10-20 1988-10-20 How to prevent slag from flowing out of the converter

Publications (2)

Publication Number Publication Date
JPH02111810A true JPH02111810A (en) 1990-04-24
JP2635721B2 JP2635721B2 (en) 1997-07-30

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Country Link
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2021109193A (en) * 2020-01-09 2021-08-02 日本製鉄株式会社 Method for feeding molten steel

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2021109193A (en) * 2020-01-09 2021-08-02 日本製鉄株式会社 Method for feeding molten steel

Also Published As

Publication number Publication date
JP2635721B2 (en) 1997-07-30

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