JPH03180419A - Refining method by blowing in converter - Google Patents

Refining method by blowing in converter

Info

Publication number
JPH03180419A
JPH03180419A JP31825489A JP31825489A JPH03180419A JP H03180419 A JPH03180419 A JP H03180419A JP 31825489 A JP31825489 A JP 31825489A JP 31825489 A JP31825489 A JP 31825489A JP H03180419 A JPH03180419 A JP H03180419A
Authority
JP
Japan
Prior art keywords
slag
blowing
mgo
converter
source
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
JP31825489A
Other languages
Japanese (ja)
Other versions
JPH0678563B2 (en
Inventor
Hideyuki Hirabashi
平橋 英行
Kiminori Hajika
公則 羽鹿
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.)
Kobe Steel Ltd
Original Assignee
Kobe Steel Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kobe Steel Ltd filed Critical Kobe Steel Ltd
Priority to JP31825489A priority Critical patent/JPH0678563B2/en
Publication of JPH03180419A publication Critical patent/JPH03180419A/en
Publication of JPH0678563B2 publication Critical patent/JPH0678563B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To enhance the yields of Mn and Fe and to inhibit the erosion of refractories by adding an MgO source to steel making slag in the last stage of refining by blowing so as to lower the potential of oxygen in the slag and to reduce the ability of the slag to capture MnO and FeO. CONSTITUTION:Molten pig iron is pretreated to remove Si, P and S. When this treated molten pig iron is refined by blowing in a converter, the concn. of MgO in slag can be increased by adding an MgO source to the slag in the early stage of refining but the m.p. of the slag is increased by the increased concn. Of MgO and it becomes difficult to allow slagging to proceed. As a result, the erosion of refractories and defective dephosphorization are caused. In order to prevent the erosion and defective dephosphorization, the MgO source is added to the slag in the last stage of refining.

Description

【発明の詳細な説明】 〔産業上の利用分野] 本発明は、予備処理された溶銑をスラグミニマムで転炉
吹錬する際に、吹止Cの的中精度を下げたりS含有率を
高めるといった問題を生ずることなく、Mn歩留りを高
めることのできる方法に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention reduces the accuracy of blowstop C and increases the S content when pretreated hot metal is subjected to converter blowing with a minimum slag. This invention relates to a method that can increase the Mn yield without causing such problems.

[従来の技術] 溶銑樋上もしくは取鍋あるいは溶銑予備処理炉等で予備
処理(脱St、脱P、脱S)された溶銑を転炉吹錬する
際においては、転炉内で脱P、脱S等を行なう必要がな
いので、造滓剤添加量は転炉耐火壁を保護し得るに足る
必要最少量に留め、造滓剤原単位を低減すると共にMn
歩留りの向上によるMn@添加量の低減を図っている。
[Prior art] When hot metal that has been pretreated (de-St, de-P, de-S) on a hot metal gutter, in a ladle, or in a hot metal pre-treatment furnace is blown into a converter, de-P and de-S are carried out in the converter. Since there is no need to perform S, etc., the amount of slag-forming agent added is kept to the minimum amount necessary to protect the converter firewall, reducing the slag-forming agent consumption rate and reducing Mn.
Efforts are being made to reduce the amount of Mn@ added by improving yield.

この場合、スラグに捕捉されるMn量を更に少なくして
Mn歩留りを高めると共に、スラグ中のT−Fe量を低
減するため、吹錬末期のスラグ中にC源(コークスや黒
鉛等)を加え、スラグ中のMn酸化物やFe酸化物を還
元して溶鋼に歩留らせ方法も提案されている。
In this case, in order to further reduce the amount of Mn trapped in the slag and increase the Mn yield, and to reduce the amount of T-Fe in the slag, a C source (coke, graphite, etc.) is added to the slag at the final stage of blowing. A method has also been proposed in which Mn oxides and Fe oxides in slag are reduced to yield molten steel.

〔発明が解決しようとする課題] ところが吹錬末期にスラグ中へC源を添加すると、該C
源の一部が溶鋼中に溶解して吹止Cの的中精度を低下さ
せるばかりでなく、C原生に不純物として含まれている
3分が溶鋼内へ取り込まれ、S濃度が高くなるといった
問題が生じてくる。
[Problem to be solved by the invention] However, when a C source is added to the slag at the final stage of blowing, the C
Not only does a part of the carbon source dissolve into the molten steel, reducing the accuracy of blow-stop C, but also the impurities contained in the carbon source are incorporated into the molten steel, increasing the S concentration. will arise.

本発明はこの様な問題点に着目してなされたものであっ
て、その目的は、予備処理を終えた溶銑をスラグミニマ
ムで転炉吹錬する際において、吹止めC的中精度の低下
やS ili度の上昇といった問題を生ずることなく、
スラグ中のMn量およびT−Fe量を低減してそれらの
歩留りを高めることのできる吹錬法を確立しようとする
ものである。
The present invention has been made in view of these problems, and its purpose is to reduce the accuracy of blowstop C accuracy and to reduce the accuracy of blow stop C when blowing hot metal that has undergone preliminary treatment in a converter furnace with minimum slag. without causing problems such as an increase in Sili
The aim is to establish a blowing method that can reduce the amount of Mn and T-Fe in slag and increase their yield.

[課題を解決する為の手段] 上記課題を解決することのできた本発明に係る転炉吹錬
法の構成は、予備処理により脱Si。
[Means for Solving the Problems] The configuration of the converter blowing method according to the present invention that can solve the above problems is that Si is removed by preliminary treatment.

脱P、脱S処理された溶銑を転炉吹錬するに当たり、吹
錬末期のスラグにMgO源を添加するところに要旨を有
するものである。
The gist of this method is to add an MgO source to the slag at the final stage of blowing when hot metal that has been subjected to P and S removal treatment is subjected to converter blowing.

[作用コ 予備処理により脱Si、脱P、脱SIA埋された溶銑を
転炉吹錬する際には、前述の如く転炉耐火壁の溶損を抑
制するに足るスラグを形成するだけでよいので、前述の
如く必要最少量の造滓剤(CaOや軽焼ドロマイト等)
を加えてスラグミニマム操業が行なわれる。従って通常
の吹錬操業に比べるとスラグ中に酸化物として損失する
Mn分やFe分は少なく抑えられるが、それでも相当量
のMn酸化物やFe酸化物がスラグに捕捉される。殊に
Mnは易酸化性のため酸化物となリスラグに捕捉され易
いので、吹錬開始前もしくは吹錬操業時の適当な時期に
Mn鉱石やMn系合金鉄等を加えてMn源を添加しても
該Mnの一部はスラグに取り込まれてロスとなる。この
様なところから、スラグ中のMn@化物を還元してMn
を溶鋼へ歩留らせる為、前述の如く吹錬末期にC源を加
えてスラグ中のMn酸化物を還元する方法が提案された
が、それに伴なって先に述べた様な問題が生じてくる。
[Operations] When blowing hot metal that has been buried in a converter to remove Si, P, and SIA through preliminary treatment, it is only necessary to form enough slag to suppress melting damage of the converter refractory wall as described above. Therefore, as mentioned above, the minimum amount of slag-forming agent (CaO, light calcined dolomite, etc.) is required.
In addition, slag minimum operation is carried out. Therefore, compared to normal blowing operations, the amount of Mn and Fe lost as oxides in the slag can be suppressed to a low level, but a considerable amount of Mn oxides and Fe oxides are still trapped in the slag. In particular, Mn is easily oxidized and is easily captured by lithium slag, which is an oxide. Therefore, Mn ore, Mn-based ferroalloy, etc. are added as a Mn source before the start of blowing or at an appropriate time during blowing operation. However, some of the Mn is taken into the slag and becomes a loss. From this point, the Mn@ compound in the slag is reduced to produce Mn.
In order to increase the yield of Mn into molten steel, a method has been proposed in which the Mn oxides in the slag are reduced by adding a C source at the end of the blowing process, as described above, but this method causes the problems mentioned above. It's coming.

そこで前述の様な問題、即ち吹止C的中精度の低下や溶
鋼中S濃度の増大といった問題を生ずることなく、Mn
歩留りを高めることのできる方法を開発しようとして種
々研究を行なった結果、吹錬の末期にMgO源を添加す
ると、スラグの酸素ポテンシャルが低下して、スラグに
捕捉されたMnが溶鋼中へ移行し易くなると共にスラグ
中のT−Fe量も減少し、MnおよびFeの歩留りを効
果的に高めることができ、しかも従来技術で指摘した様
な問題は一切生じなくなることを知った。
Therefore, the Mn
As a result of conducting various studies in an attempt to develop a method that could increase the yield, it was found that adding an MgO source at the final stage of blowing lowers the oxygen potential of the slag and causes Mn trapped in the slag to migrate into the molten steel. It has been found that the amount of T-Fe in the slag is reduced and the yield of Mn and Fe can be effectively increased, and the problems pointed out in the prior art do not occur at all.

この様な効果が得られる理由は次の様に考えられる。即
ち、スラグ中にMgO源を添加してMgO濃度を高める
とスラグ中の酸素ポテンシャルが低下し、T−Fe量が
低減すると共にMn捕捉能力も低下してくる。たとえば
第1図は製鋼スラグにおけるFeOの等活量線図を示し
たものであり、この図からも明らかである様に、スラグ
中のMgO量が増加するにつれてスラグの酸素ポテンシ
ャルは低下してくる。また第2図は、S i O,−C
aO−MgO−Fern系における各成分の飽和曲線図
を示したものであり、この図からは、白抜き矢印[A]
 で示す通りスラグ中のMgO量を増加するとFern
の飽和量が低下し、スラグの酸素ポテンシャルが低下す
ることを確認できる。
The reason why such an effect can be obtained is considered as follows. That is, when an MgO source is added to the slag to increase the MgO concentration, the oxygen potential in the slag decreases, the amount of T-Fe decreases, and the Mn trapping ability also decreases. For example, Figure 1 shows the isoactivity diagram of FeO in steelmaking slag, and as is clear from this diagram, as the amount of MgO in the slag increases, the oxygen potential of the slag decreases. . Moreover, FIG. 2 shows S i O, -C
This shows a saturation curve diagram of each component in the aO-MgO-Fern system, and from this diagram, the white arrows [A]
As shown in , when the amount of MgO in the slag is increased, Fern
It can be confirmed that the saturation amount of slag decreases and the oxygen potential of the slag decreases.

かくして吹錬末期の製鋼スラグ中!:MgO源を添加す
ることによってスラグの酸素ポテンシャルが低減し、ス
ラグのMnOおよびFeO捕捉能が低下する結果、余剰
のFeおよびMnは溶鋼へ移行し、MnおよびFeの歩
留りが向上する。従ってMn量調整のためのMn源添加
量を従来例に比べて減少することが可能となる。しかも
MgOは高融点(約2800℃)であるので、製鋼スラ
グにMgO源を添加するとスラグは高融点となって粘性
が高まり、スラグフォーよングが抑制されると共に、転
炉耐火壁の溶損抑制効果も高められる。またMgO源と
してはMgOのほか軽焼ドロマイト(CaO・Mg0)
、生ドロマイト(Ca COs ・M g COs )
 、金属Mg等が使用されるが、これらにはCが含まれ
ていないので吹止Cの的中精度C悪影響を及ぼす恐れが
なく、またS等の有害成分も殆んど含まれていないので
、溶鋼のS濃度を高めるといった問題を生ずることもな
い。
Thus, steelmaking slag at the final stage of blowing! : By adding the MgO source, the oxygen potential of the slag is reduced, and the MnO and FeO trapping ability of the slag is reduced. As a result, excess Fe and Mn are transferred to molten steel, and the yield of Mn and Fe is improved. Therefore, the amount of Mn source added for adjusting the amount of Mn can be reduced compared to the conventional example. Moreover, since MgO has a high melting point (approximately 2800°C), adding an MgO source to steelmaking slag makes the slag have a high melting point and increases viscosity, suppressing slag foaming and causing melting of the converter firewall. The suppressive effect is also enhanced. In addition to MgO, light calcined dolomite (CaO/Mg0) is an MgO source.
, raw dolomite (Ca COs ・M g COs )
, metallic Mg, etc. are used, but since these do not contain C, there is no risk of adversely affecting the accuracy of the blow-stop C, and they also contain almost no harmful components such as S. , there is no problem of increasing the S concentration of molten steel.

ところでMgO源の添加時期としては、吹錬の初期に添
加してスラグのMgO濃度を当初から高くしておくこと
も可能であるが、この場合は、MgOの濃度の上昇によ
りスラグの融点が上昇し、スラグの滓化が進行し難くな
る。その結果、未滓化に伴なう耐火物溶損、脱P反応不
良といった問題が生じ易くなるので、好ましいのは吹錬
の末期(たとえば吹止めの1〜2分程度前)に添加する
のがよく、また経済性を加味すると好ましい添加量はM
gO換算で溶銑1トン当たり0.1〜5kg程度である
By the way, as for the timing of adding the MgO source, it is possible to increase the MgO concentration in the slag from the beginning by adding it at the beginning of blowing, but in this case, the melting point of the slag will rise due to the increase in the MgO concentration. However, it becomes difficult for the slag to become slag. As a result, problems such as melting of the refractory and poor dephosphorization reaction due to unslag formation tend to occur, so it is preferable to add it at the final stage of blowing (for example, about 1 to 2 minutes before the end of blowing). is good, and taking economic efficiency into consideration, the preferable addition amount is M
In terms of gO, it is about 0.1 to 5 kg per ton of hot metal.

[実施例] 下記の条件で、グループ■および■について夫々30チ
ヤージの転炉吹錬実験を行ない、得られた溶鋼のMn歩
留りおよび吹止C量を比較した。
[Example] Under the following conditions, a converter blowing experiment of 30 charges was conducted for each of Groups (1) and (2), and the Mn yield and blow-off C amount of the obtained molten steel were compared.

グループ■(比較例):吹止1分前にコークスを2.5
kg/を添加(30 チャージ) グループ■(実施例):吹止1分前に軽焼ドロマイトを
2.5kg/を添加 (30チヤージ) (実験条件)ニゲループ[株]、■共通災箆里旦・・・
溶銑95トン+スクラップ5トン4社工1− C: 4
.00〜4.1G、  S i : t r 。
Group ■ (comparative example): 2.5 liters of coke 1 minute before blow-off
Added 2.5 kg/kg/kg (30 charges) Group ■ (Example): Added 2.5 kg/lightly calcined dolomite 1 minute before blow-off (30 charges) (Experimental conditions) Nigelup [Co., Ltd.], ■ Common Disaster Ridan ...
95 tons of hot metal + 5 tons of scrap 4 companies 1-C: 4
.. 00-4.1G, Si: tr.

M  n  :  0.50〜0.60.  P  :
  0.010 〜0.013.S : 0.014〜
0.017 、温度=1300〜1320℃ 遣捜1 ・・・Ca O: 7.3kg/)ン、軽焼ド
ロマイト :  5.2kg/)ンお よびSin  
2 :t、okg/))を、吹錬開始直後に前装入吸夏
丘エニ2・・・気体酸素はすべて上吹き酸素ランスより
一定送酸速度(2,8ONm’/分・トン)で供給、ラ
ンス高さは湯面より2000m+*に設定した。
Mn: 0.50-0.60. P:
0.010 to 0.013. S: 0.014~
0.017, Temperature = 1300-1320°C Kensou 1...CaO: 7.3kg/)n, light calcined dolomite: 5.2kg/)n, and Sin
2:t, OKG/)) is pre-charged immediately after the start of blowing. All gaseous oxygen is supplied from the top blowing oxygen lance at a constant oxygen supply rate (2.8 ONm'/min/ton). The supply and lance height was set at 2000m+* from the hot water level.

i裏ゑ且・・・吹止C: 0.25%、吹止温度: 1
B60℃となる様に制御した。
i Back end...Blow end C: 0.25%, Blow end temperature: 1
The temperature was controlled to be 60°C.

結果を平均値として第1表に示す。The results are shown in Table 1 as average values.

第 表 第1表からも明らかである様に、従来法(グループ■)
では吹止C量が目標値よりもかなり高くなると共にその
標準偏差も大きく、Mn歩留りも相対的に低いのに対し
、本発明(グループ■)では吹止Cの増加が認められず
またその標準偏差も小さく、Mn歩留りは約2%向上し
ている。尚上記の吹錬実験で、吹止後の耐火物表面に対
するスラグコーティング状況を目視観察したところ、グ
ループ■(本発明法)の方が、スラグの融点上昇に伴な
う粘性向上により優れたコーテイング性を発揮している
ことが確認された。
As is clear from Table 1, the conventional method (group ■)
In contrast, in the present invention (Group ■), no increase in blow-off C was observed, and the standard deviation was also large and the Mn yield was relatively low. The deviation is also small, and the Mn yield is improved by about 2%. In the above-mentioned blowing experiment, when we visually observed the state of slag coating on the refractory surface after blowing, we found that Group ■ (method of the present invention) had better coating due to the improvement in viscosity caused by the rise in the melting point of the slag. It was confirmed that they were demonstrating their sexuality.

[発明の効果] 本発明は以上の様に構成されており、高レベルの吹止C
的中精度を維持しつつ、且つS濃度を高めることなくM
n歩留りを向上させることができ、且つスラグ中T−F
eの低減によりFeロスも低減することができる。しか
もスラグの粘性向上により転炉耐火物の溶損も抑制する
ことができるなど、実用社印した効果を得ることができ
る。
[Effects of the Invention] The present invention is configured as described above, and has a high level of blowout C.
M while maintaining accuracy and without increasing S concentration.
n Yield can be improved, and T-F in slag can be improved.
Fe loss can also be reduced by reducing e. Moreover, it is possible to obtain practical effects such as the ability to suppress melting loss of converter refractories by improving the viscosity of the slag.

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

第1図は製鋼スラグにおけるFeOの等活量線図、第2
図はS 10 x −Ca O−M g O−FeOn
系スラグにおける各成分の飽和曲線図を示したものであ
る。
Figure 1 is the isoactivity diagram of FeO in steelmaking slag, Figure 2
The figure shows S 10 x -Ca O-M g O-FeOn
This figure shows a saturation curve diagram of each component in the system slag.

Claims (1)

【特許請求の範囲】[Claims] 予備処理により脱Si、脱P、脱S処理された溶銑を転
炉吹錬するに当たり、吹錬末期のスラグにMgO源を添
加することを特徴とする転炉吹錬方法。
A converter blowing method characterized by adding an MgO source to slag at the final stage of blowing when hot metal that has been subjected to preliminary treatment to remove Si, P, and S is subjected to converter blowing.
JP31825489A 1989-12-07 1989-12-07 Converter blowing method Expired - Lifetime JPH0678563B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31825489A JPH0678563B2 (en) 1989-12-07 1989-12-07 Converter blowing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31825489A JPH0678563B2 (en) 1989-12-07 1989-12-07 Converter blowing method

Publications (2)

Publication Number Publication Date
JPH03180419A true JPH03180419A (en) 1991-08-06
JPH0678563B2 JPH0678563B2 (en) 1994-10-05

Family

ID=18097155

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31825489A Expired - Lifetime JPH0678563B2 (en) 1989-12-07 1989-12-07 Converter blowing method

Country Status (1)

Country Link
JP (1) JPH0678563B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007254839A (en) * 2006-03-24 2007-10-04 Jfe Steel Kk Melting method of high phosphorus steel

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110343803B (en) * 2019-07-31 2020-12-11 西安建筑科技大学 Smelting method for applying magnesium reducing slag to converter steelmaking

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007254839A (en) * 2006-03-24 2007-10-04 Jfe Steel Kk Melting method of high phosphorus steel

Also Published As

Publication number Publication date
JPH0678563B2 (en) 1994-10-05

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