JPS6056201B2 - Hot metal processing method - Google Patents

Hot metal processing method

Info

Publication number
JPS6056201B2
JPS6056201B2 JP16785479A JP16785479A JPS6056201B2 JP S6056201 B2 JPS6056201 B2 JP S6056201B2 JP 16785479 A JP16785479 A JP 16785479A JP 16785479 A JP16785479 A JP 16785479A JP S6056201 B2 JPS6056201 B2 JP S6056201B2
Authority
JP
Japan
Prior art keywords
hot metal
blowing
converter
processing method
gas
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
Application number
JP16785479A
Other languages
Japanese (ja)
Other versions
JPS5690913A (en
Inventor
努 野崎
恭二 中西
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
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 Kawasaki Steel Corp filed Critical Kawasaki Steel Corp
Priority to JP16785479A priority Critical patent/JPS6056201B2/en
Publication of JPS5690913A publication Critical patent/JPS5690913A/en
Publication of JPS6056201B2 publication Critical patent/JPS6056201B2/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C1/00Refining of pig-iron; Cast iron
    • C21C1/02Dephosphorising or desulfurising

Description

【発明の詳細な説明】 この発明は、溶銑処理方法に関し、とくにその有利な不
純物除去手段の開発成果を提案しようとするものである
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a hot metal treatment method, and particularly aims to propose the development results of an advantageous means for removing impurities.

この発明により溶銑処理方法は、以下のべるような製鋼
精錬過程への適用にとくに有利であり、この場合、該精
錬のための溶銑予備処理としても有用である。
The method for treating hot metal according to the present invention is particularly advantageous in application to the following steelmaking and refining process, and in this case, it is also useful as a pretreatment of hot metal for the refining.

近年鋼材品質に関しその成分および材質の規格ないしは
要請が甚だ厳しく、このため鋼中の不純物とくにりん、
いおうの除去方法に関心が払われている。
In recent years, standards and requirements for steel components and materials have become extremely strict, and as a result, impurities in steel, especially phosphorus,
There is a lot of interest in how to remove sulfur.

一方では転炉吹錬の安定化、鉄歩留りの向上そして低コ
スト操業が強く叫ばれている。このような情勢のもとで
製銑、製鋼法の見直しが必要となつてきている。転炉操
業の安定に関しては装入溶銑の成分が一定していること
が望ましく、従つて転炉装入前に脱りん、脱硫ならびに
脱けいを行つておくことが望まれ、その方法としては溶
銑のCが高く酸素ポテンシャルが低い時点で脱硫し、次
に酸化状態にして脱けい、脱りん処理を行うことが考え
られる。
On the other hand, there are strong calls for stabilization of converter blowing, improvement of iron yield, and low-cost operation. Under these circumstances, it has become necessary to review ironmaking and steelmaking methods. For stable converter operation, it is desirable that the charged hot metal has a constant composition. Therefore, it is desirable to perform dephosphorization, desulfurization, and desiliconization before charging into the converter. It is conceivable to desulfurize the carbon at a point when the C content is high and the oxygen potential is low, and then bring it into an oxidized state to perform desulfurization and dephosphorization treatments.

しカルこのような工程は通常多段樋方式の半連続製鋼法
に似た組合せとなつて、熱損失が大きく省エネルギーの
点から問題が多い。すなわちかような溶銑予備処理の目
的は、りん、いおうおよびけい素の除去にあるがそれぞ
れの反応を1つ1つ分離した形で処理することは熱損失
の面でもまたコスト的にも好ましくないのである。そこ
でこれらの反応を同時に行うことに関し、底吹き転炉に
着目した。
This type of process is usually a combination similar to the multi-stage semi-continuous steel manufacturing process, which causes large heat loss and has many problems in terms of energy conservation. In other words, the purpose of such hot metal pretreatment is to remove phosphorus, sulfur, and silicon, but it is undesirable in terms of heat loss and cost to treat each reaction separately. It is. Therefore, in order to perform these reactions simultaneously, we focused on a bottom-blown converter.

底吹き転炉は攪拌性が秀れていてメタルーズラグ間の反
応を有利に促進できるので熱効率も良いことに加えて純
酸素ガスのみならず窒素あるいはアルゴンなどの不活性
ガスを必要の都度容易に切替え使用できることから溶銑
の予備処理への適用を検討し、実験を重ねてその方法を
確立したものである。この発明は、底吹き転炉またはそ
れに類似の吹・精容器内の溶銑に、主として酸化性ガス
の底吹きによる脱けいを施し、引続き非酸化性ガスの底
吹きに切替えて脱硫処理を行いその後再び酸化性ガスに
切替えこれを吹錬兼用の搬送ガスとして脱りん剤ととも
に底吹きして軽脱炭および脱りんを行う、プロセスを順
次に進行させることからなる溶銑処理方法である。
The bottom-blown converter has excellent agitation and can advantageously promote the reaction between metal loose lags, so it has good thermal efficiency and can easily switch between pure oxygen gas and inert gases such as nitrogen or argon whenever necessary. Since this method can be used, we considered applying it to the preliminary treatment of hot metal, and after repeated experiments, we established the method. This invention desilicates hot metal in a bottom-blowing converter or similar blowing/refining vessel by mainly bottom-blowing oxidizing gas, then switching to bottom-blowing non-oxidizing gas to perform desulfurization treatment, and then This hot metal treatment method consists of sequentially proceeding with the process of switching to oxidizing gas again and using it as a carrier gas for blowing and bottom blowing it together with a dephosphorizing agent to perform light decarburization and dephosphorization.

この発明によればそれに従う溶銑処理によつて所定のC
,Si,Mn,P,Sに成分調整した後排滓してそのま
ま底吹き転炉(Q−BOP炉)内または普通の上吹き転
炉に装入してスラグなしの吹錬にも供することができる
According to this invention, a predetermined C can be achieved by the hot metal treatment according to the method.
After adjusting the composition to , Si, Mn, P, and S, the slag is discharged and charged directly into a bottom-blowing converter (Q-BOP furnace) or a normal top-blowing converter for slag-free blowing. Can be done.

この発明の処理は上記のようにして底吹き転炉を用いて
有利に行われるのであるが、その吹錬機能が同等である
ような類似の溶銑容器を用い得るのはいうまでもない。
Although the process of the present invention is advantageously carried out using a bottom blowing converter as described above, it goes without saying that similar hot metal vessels having the same blowing function may be used.

炉容5トンのQ−BOP炉による実験概要は次のとおり
である。ます高炉溶銑をQ−BOP炉に装入後、微粉状
石灰を純酸素ガスで炉底羽口から吹込み昇温と脱けいを
行う。
The outline of the experiment using a Q-BOP reactor with a reactor capacity of 5 tons is as follows. After the blast furnace hot metal is charged into the Q-BOP furnace, pulverized lime is blown in through the bottom tuyere with pure oxygen gas to raise the temperature and desiliconize it.

このとき必ずしも石灰を用いなくてもよいが、スピツテ
イング防止と、引続く脱硫工程の効率を上げるためには
石灰を用いた方が良好な成績を示した。この脱けいプロ
セスを終了後搬送ガスをN2に切換えてCaOを炉底羽
口から吹込み脱硫を行う。なおこの脱硫工程にCac2
を使うときには排滓が必要である。その後に再び酸素ガ
スに切替えて脱りん剤を吹込みつつ脱炭、脱りんを行う
。この処理によりCは1〜3%、Siはトレース、Mn
は0.2%台そしてPは0.02〜0.03%またはS
は0.01%台の成績が得られた。このような処理を行
つた溶銑は山転炉あるいはQ−BOP炉に装入し−て脱
炭工程のみを行えばよい。以上の方法で底吹き転炉を利
用して溶銑予備処理を行う場合の模式図は第1図の如く
である。
At this time, it is not necessary to use lime, but in order to prevent spitting and increase the efficiency of the subsequent desulfurization process, the use of lime showed better results. After this desulfurization process is completed, the carrier gas is switched to N2, and CaO is blown into the furnace through the bottom tuyere to perform desulfurization. In addition, Cac2 is used in this desulfurization process.
It is necessary to remove the slag when using it. After that, the gas is switched to oxygen again and decarburization and dephosphorization are carried out while blowing in a dephosphorizing agent. Through this process, C is 1-3%, Si is trace, Mn is
is in the 0.2% range and P is 0.02-0.03% or S
Results were obtained in the 0.01% range. The hot metal that has undergone such treatment may be charged into a mountain converter or a Q-BOP furnace and subjected to only the decarburization process. A schematic diagram of the case where hot metal preliminary treatment is carried out using a bottom blowing converter using the above method is shown in FIG.

以上のプロセスに従う実施例をここに説明する。高炉か
ら出銑した溶銑を脱硫せずに5トン底吹き転炉に装入し
た。
An embodiment according to the above process will now be described. Hot metal tapped from a blast furnace was charged into a 5-ton bottom blowing converter without desulfurization.

装入量は5.5トンであり、装入時の溶銑温度は130
0℃、溶銑成分はC/4.5%、Si/0.6%、Mn
/0.35%、P/0.117%、S/0.030%で
あつた。先ず脱けいプロセスは送酸量毎分2NI/TO
nの酸素でCaOを15k9/TOn吹込んだ、この処
理によりC/4.2%、Si/0.01%、Mn/0.
30%、P/0.082%、S/0.030%となつた
The charging amount was 5.5 tons, and the hot metal temperature at the time of charging was 130
0℃, hot metal components are C/4.5%, Si/0.6%, Mn
/0.35%, P/0.117%, and S/0.030%. First, in the desiliconization process, the oxygen supply rate is 2 NI/TO per minute.
CaO was blown at 15k9/Ton with oxygen of n, and this treatment resulted in C/4.2%, Si/0.01%, Mn/0.
30%, P/0.082%, S/0.030%.

吹込みガスN2に切換え毎分2Nイ/TOnの窒素でC
aOを10k9/TOn吹込んだところ上記成分はC/
4.2%、Si/0.01%、Mn/0.31%、P/
0.082%、S/0.007%となつた。次に再び0
,ガスに切換えCaO7O%、鉄鉱石20%、Na2C
QlO%の脱燐剤を20k9/TOnを送酸量毎分2.
5Nd/TOnで吹込んだ。
Switch to blowing gas N2 and 2N/Ton nitrogen per minute
When aO was injected at 10k9/Ton, the above components were C/
4.2%, Si/0.01%, Mn/0.31%, P/
It became 0.082% and S/0.007%. then 0 again
, Switched to gas CaO7O%, iron ore 20%, Na2C
A dephosphorizing agent of QlO% was added at an oxygen flow rate of 20k9/TOn per minute.
It was injected with 5Nd/Ton.

これにより得られた溶銑処理後の最終成分はC/3.8
%、Si/TracelMn/0.20%、P/0.0
17%、S/0.006%であつた。なおこのときの温
度はu羽℃であつた。このようにして溶銑成分のバラツ
キが少なくなるのでその後に供した転炉吹錬での安定化
ができるのみならず、すでに溶銑中のC以外は所定の値
に到達していることから転炉内では脱炭のみを行えばよ
く、この段階で転炉吹錬にCaOの添加はほとんど必要
なく添加する場合でも10kg/TOn以下で済むよう
になるので従来転炉スラグ中へ逸散していた成分がなく
なる分だけ鉄歩留りが向上しまた耐火物寿命が向上する
。なおソーダ灰を用いる同時脱りん脱硫法が、上記の溶
銑予備処理のために最近注目されているけれども、この
場合にはソーダ灰30k9/TOnを必要とするのでこ
れと比べてもこの発明は副原料原単価が安くまた熱損失
が少ないなど多大のメリットがある。
The final composition after hot metal treatment obtained by this is C/3.8
%, Si/TracelMn/0.20%, P/0.0
It was 17% and S/0.006%. Note that the temperature at this time was 0.degree. In this way, the variation in the hot metal components is reduced, which not only makes it possible to stabilize the subsequent converter blowing process, but also because the contents of the hot metal other than C have already reached the predetermined values. In this case, only decarburization needs to be performed, and at this stage there is almost no need to add CaO to the converter blowing, and even if it is added, it will be less than 10 kg/TOn, so the components that conventionally escaped into the converter slag can be removed. The iron yield improves and the life of the refractories increases by the amount that is eliminated. Although the simultaneous dephosphorization and desulfurization method using soda ash has recently been attracting attention for the hot metal pretreatment described above, in this case, 30k9/TOn of soda ash is required, so even compared to this method, the present invention is inferior. It has many advantages such as low raw material cost and low heat loss.

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

第1図はこの発明を溶銑予備処理に適用した製鋼過程の
系統図である。
FIG. 1 is a system diagram of a steelmaking process in which the present invention is applied to hot metal pretreatment.

Claims (1)

【特許請求の範囲】[Claims] 1 底吹き転炉またはそれに類似の吹精容器内の溶銑に
、主として酸化性ガスの底吹きによる脱けい処理を施し
、引き続き非酸化性ガスの底吹きに切替えて脱硫処理を
行い、その後再び酸化性ガスに切替えこれを吹錬兼用の
搬送ガスとして脱りん剤とともに底吹きして軽脱炭およ
び脱りんを行う、プロセスを順次に進行させることを特
徴とする溶銑処理方法。
1 The hot metal in a bottom blowing converter or similar blowing vessel is subjected to desulfurization treatment mainly by bottom blowing with oxidizing gas, then switched to bottom blowing with non-oxidizing gas to perform desulfurization treatment, and then oxidized again. A hot metal processing method characterized by sequentially proceeding with the process of switching to a carbonaceous gas and using it as a carrier gas for blowing and bottom-blowing it together with a dephosphorizing agent to perform light decarburization and dephosphorization.
JP16785479A 1979-12-24 1979-12-24 Hot metal processing method Expired JPS6056201B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16785479A JPS6056201B2 (en) 1979-12-24 1979-12-24 Hot metal processing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16785479A JPS6056201B2 (en) 1979-12-24 1979-12-24 Hot metal processing method

Publications (2)

Publication Number Publication Date
JPS5690913A JPS5690913A (en) 1981-07-23
JPS6056201B2 true JPS6056201B2 (en) 1985-12-09

Family

ID=15857314

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16785479A Expired JPS6056201B2 (en) 1979-12-24 1979-12-24 Hot metal processing method

Country Status (1)

Country Link
JP (1) JPS6056201B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63148801U (en) * 1987-03-20 1988-09-30

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63148801U (en) * 1987-03-20 1988-09-30

Also Published As

Publication number Publication date
JPS5690913A (en) 1981-07-23

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