JPS59185715A - Pretreatment of molten iron - Google Patents

Pretreatment of molten iron

Info

Publication number
JPS59185715A
JPS59185715A JP6140783A JP6140783A JPS59185715A JP S59185715 A JPS59185715 A JP S59185715A JP 6140783 A JP6140783 A JP 6140783A JP 6140783 A JP6140783 A JP 6140783A JP S59185715 A JPS59185715 A JP S59185715A
Authority
JP
Japan
Prior art keywords
hot metal
molten iron
vessel
container
flux
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.)
Pending
Application number
JP6140783A
Other languages
Japanese (ja)
Inventor
Naoto Tsutsumi
直人 堤
Yoshimasa Mizukami
水上 義正
Takaharu Yoshida
吉田 隆春
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
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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP6140783A priority Critical patent/JPS59185715A/en
Publication of JPS59185715A publication Critical patent/JPS59185715A/en
Pending 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)

Abstract

PURPOSE:To shorten the treatment time, to prevent a temp. loss and to reduce a load on the operation of a converter by bringing dropping molten iron into contact with a flux for refining in the 1st vessel while discharging molten iron into the vessel, and successively discharging the pretreated molten iron into the 2nd vessel. CONSTITUTION:While discharging molten iron 3 from a vessel 1 such as a torpedo car into the 1st vessel 2, a flow 3' of the dropping molten iron is brought into contact with a flux 4 for refining, and the molten iron is pretreated in the vessel 2. The pretreated molten iron is successively discharged into the 2nd vessel 5. At this time, a weir 6 is placed in the vessel 2 to prevent slag from entering the molten iron to be discharged. Furthermore a lower weir 6' may be placed as necessary.

Description

【発明の詳細な説明】 本発明は溶銑の予備処理方法に関するものである。従来
より、鋼に対し高度な品質が要求され、高級品質に対処
するため、転炉吹錬に加え、溶銑の予備処理が不可欠と
なっており、溶銑中のSl、P、S等について予備処理
が行われているのは周知である。特に低硫鋼を溶製する
ために溶銑脱硫がさかんに行われてきたし、又最近では
Si、  Pについても積極的な処理方法の開発が進め
られている。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for pre-treating hot metal. Traditionally, high quality steel has been required, and in order to achieve high quality, in addition to converter blowing, preliminary treatment of hot metal has become essential. It is well known that this is being done. In particular, desulfurization of hot metal has been actively carried out to produce low sulfur steel, and recently active treatment methods for Si and P have been actively developed.

たとえは、炉外溶鉄脱硫法においては、混銑車あるいは
溶銑鍋において、インジェクション 。
For example, in the out-of-furnace molten iron desulfurization method, injection is performed in the pig iron mixer car or hot metal pot.

もしくは攪拌法により、ソーダ灰、生石灰、カーバイト
といった脱硫剤を溶銑と接触させる方法が行われ、又脱
珪法においては、高炉炉床あるいは受銑後の混銑車内に
おいて、酸化鉄、生石灰等を投入する方法が行われ、脱
燐処理も同様に生石灰、ソーダ灰なとの脱燐剤を、酸素
源とともに溶銑に投入し、攪拌する方法により行われて
いる。
Alternatively, a stirring method is used in which a desulfurizing agent such as soda ash, quicklime, or carbide is brought into contact with hot metal.In the desiliconization method, iron oxide, quicklime, etc. Similarly, dephosphorization treatment is carried out by adding a dephosphorizing agent such as quicklime or soda ash to hot metal along with an oxygen source and stirring.

これらの方法は、反応機構的に脱硫が近元性雰囲気下、
脱珪、脱燐が酸化性雰囲気下で促進されるため、同時処
理が困難であること、又同−・条件下における脱珪、脱
燐反応も、脱珪が脱燐よりも優先的に反応が進み、作業
効率上、脱珪処理時に発生するスラグを排滓してのちに
脱燐処理にかがらねばならぬことにより、長い処理時間
を要し、その間の温度降下をまぬがれない。
These methods require desulfurization to occur in a near-atomic atmosphere due to the reaction mechanism.
Since desiliconization and dephosphorization are promoted in an oxidizing atmosphere, it is difficult to carry out simultaneous treatment, and desiliconization and dephosphorization reactions under the same conditions also have a tendency for desiliconization to occur preferentially over dephosphorization. In terms of work efficiency, the slag generated during the desiliconization process must be removed before the dephosphorization process takes place, resulting in a long process time and a drop in temperature during the process.

本発明はこのような欠点を有利に解決するためになされ
たもので、溶acの予備処理において、工程を工夫し、
処理を連続化することにより、排滓を容易とし、処理時
間を短縮し、温度ロスを防止し、溶銑中へのスラグの流
出防止、高炉から転炉に至る精錬ハンドリングの向上、
高い温度での溶銑転炉装入による転炉操業負荷の低減を
目的とするものである。その構成要件は溶銑を第1容器
へ払い出しつつ、該容器内で落下溶銑と精錬用フラック
スを接触せしめ、順次第2容器へ払い出すことを特徴と
する溶銑の予備処理方法に関するも−のである。
The present invention has been made to advantageously solve these drawbacks, and in the preliminary treatment of molten AC, the process is devised and
Continuous processing makes it easier to remove slag, shorten processing time, prevent temperature loss, prevent slag from flowing into the hot metal, and improve refining handling from the blast furnace to the converter.
The purpose is to reduce the operating load of the converter by charging hot metal into the converter at high temperatures. Its constituent features relate to a hot metal pretreatment method characterized by discharging the hot metal into a first container, bringing the falling hot metal into contact with refining flux within the container, and discharging the hot metal into two containers in sequence.

すなわち、本発明は、たとえば溶銑を高炉より直接第1
容器へ払い出し、又はたとえば高炉より転炉に至る運搬
過程において処理を行うもので、たとえば混銑車、取鍋
等を用い、これに、高炉から受銑し、次いで、製鋼炉へ
装入する取鍋へ払い出す秤量工程の際に溶銑の落下エネ
ルギーを攪拌力として有効に利用し、脱燐、脱珪、脱硫
といった精錬処理を施すものである。
That is, in the present invention, for example, hot metal is directly transported from the blast furnace to the first
It is discharged into a container or treated during the transportation process from a blast furnace to a converter, for example, using a mixer car, a ladle, etc., and a ladle that receives pig iron from a blast furnace and then charges it to a steelmaking furnace. During the weighing process, the falling energy of hot metal is effectively used as stirring force to perform refining processes such as dephosphorization, desiliconization, and desulfurization.

これを図面により、より具体的に述べると、図示のごと
く、容器1(混銑車等)から、第1容器2へ溶銑3を払
い出しつつ、その溶銑落下流3′と精錬用フラックス4
とを接触させ、第1容器z内におい゛て、溶銑の予備処
理を施し、処理済の溶銑を順次第2容器5へ払い出す。
To describe this more specifically with reference to the drawings, as shown in the figure, while discharging hot metal 3 from a container 1 (such as a pig iron mixing car) to the first container 2, the falling flow 3' of the hot metal and the refining flux 4
The hot metal is brought into contact with the first container z, and the hot metal is pre-treated in the first container z, and the treated hot metal is sequentially discharged into the second container 5.

このように、第1容器2へ溶銑を払い出し、そこで処理
を行い、次いで、第2容器5へ払い出す工程を連続的に
行うもので、溶銑を払い出しながら予備処理するところ
に大きな特徴をもつものである。上記第1容器2には、
図に示すごとく、堰6を設けることが好ましく第2容器
5の上部にスラグ(フラ、ンクス)が位置しないように
配慮することにより、払い出し溶銑中へのスラグ(フラ
ックス)のまきこみ防止が図れる。又払い出し終了間際
に、堰6の下端よりも低い位置にスラグ(フラックス)
面が到達した場合にも、第1容器2を若干傾ける事、に
よりスラグ(フラックス)の混入を最小限に防ぐことが
できる。
In this way, the process of discharging hot metal into the first container 2, processing there, and then discharging it to the second container 5 is performed continuously, and a major feature is that the pretreatment is performed while discharging the hot metal. It is. In the first container 2,
As shown in the figure, it is preferable to provide a weir 6 to prevent slag (flux) from being located in the upper part of the second container 5, thereby preventing slag (flux) from being mixed into the discharged hot metal. Also, just before the end of dispensing, slag (flux) is deposited at a position lower than the lower end of weir 6.
Even when the surface reaches the surface, by slightly tilting the first container 2, mixing of slag (flux) can be prevented to a minimum.

図面には、例示として溶銑上に浮遊したスラグ(フラッ
クス)の移動を制限する上堰6を例示しているが、堰の
設置は、溶銑の予備処理の効率向上を図るもので、これ
により溶銑と精錬用フラックスとが、充分接触し、又払
い出し溶銑中へのスラブ(フラックス)のまき込み防止
を図るもので、位置、形状、個数等は、処理に応じて適
宜決定する。したがって、処理目標に応じて、第1容器
の底面より、点線で図示したごとく上堰6′を立設させ
てもよい。
The drawing shows, as an example, an upper weir 6 that restricts the movement of slag (flux) floating on the hot metal. This is to ensure sufficient contact between the flux and the refining flux and to prevent the slab (flux) from being mixed into the discharged hot metal.The position, shape, number, etc. of the flux are determined as appropriate depending on the processing. Therefore, depending on the processing target, an upper weir 6' may be provided upright from the bottom of the first container as shown by the dotted line.

本発明の予備処理においては、成分目標に合わせて、脱
燐、脱珪、脱硫を施せばよく、その際の処理剤(精錬用
フラックス)には、これまで用いられているものが使用
でき、たとえば脱燐剤としてはCaO1CaF2、Ca
0文2の混合物、焼成フラックス、Na2 co3等を
酸素源としての金属酸化物(酸化鉄等)と共に用いるこ
とができ、脱珪剤としては焼結鉱、ミルスケール、酸化
鉄等を用いることができる。又フラックス原単位を調製
することにより、脱珪、脱燐を同時処理することもでき
る。脱硫剤としては、CaC2、CaO、Na2 GO
3等のフラックスを用いることができる。
In the preliminary treatment of the present invention, dephosphorization, desiliconization, and desulfurization may be performed in accordance with the component target, and the treatment agent (refining flux) used in this case can be any one that has been used up to now. For example, as a dephosphorizing agent, CaO1CaF2, Ca
A mixture of 0 sentence 2, calcined flux, Na2 CO3, etc. can be used together with a metal oxide (iron oxide, etc.) as an oxygen source, and sintered ore, mill scale, iron oxide, etc. can be used as a desiliconizing agent. can. Furthermore, by adjusting the flux consumption rate, desiliconization and dephosphorization can be performed simultaneously. As a desulfurizing agent, CaC2, CaO, Na2 GO
3 grade flux can be used.

落下溶銑と精錬用フラックスとを接触させるため、精錬
用フラックスの第1容器内への投入方法としては、分割
投入、一括投入、連続投入等の方法がある。又、溶銑流
の落下位置へ投入すると良い効果が得られる。
In order to bring the falling hot metal into contact with the refining flux, methods for charging the refining flux into the first container include dividing charging, batch charging, and continuous charging. In addition, a good effect can be obtained if it is placed in the position where the hot metal flow falls.

次に本発明を実施例に基づき説明する。Next, the present invention will be explained based on examples.

実施例1 高炉より150を混銑車に受銑し、混銑車内にて脱硫処
理を施したのちの溶銑(成分重量%:Ct、82、Si
 O,43、Mn O,E15 、  Po、08? 
、So、0032残Fe並びに不純物、溶銑温度138
0°C)を、前記第1容器(深さ1500mm、長さ?
OCIOmm、巾2000mm、容器中央部に高さ80
0mmの堰を設置)に、10t/分の速度で払い出しつ
つ、同時にフラックス(成分重量%:Ca070.  
GaF230) 20kg/l−pigをミルスケール
30Kg/l−pigとともに投入(3分おきに分割投
入)したところ、払い出し終了後の溶銑装入鍋(第2容
器)内溶銑(成分重量%:C4,52、Si O,09
、Mn0038、Po、003 、  So、0021
、残Feならびに不純物、溶銑温度131O°C)は、
優れた脱燐ならびに脱珪効果を示し、温度降下も少なく
、且つ第2容器内のスラグ量も厚みで20mm程と少な
く、次工程の製鋼精錬に全く支障なく用いることができ
た。
Example 1 Hot metal (component weight%: Ct, 82, Si
O, 43, Mn O, E15, Po, 08?
, So, 0032 residual Fe and impurities, hot metal temperature 138
0°C) in the first container (depth 1500mm, length ?
OCIOmm, width 2000mm, height 80mm in the center of the container
At the same time, flux (component weight %: Ca070.
When 20 kg/l-pig of GaF230) was charged together with mill scale 30 kg/l-pig (split injection every 3 minutes), hot metal (component weight %: C4, 52, SiO, 09
, Mn0038, Po, 003, So, 0021
, residual Fe and impurities, hot metal temperature 131O°C),
It exhibited excellent dephosphorization and desiliconization effects, had a small temperature drop, and the amount of slag in the second container was as small as 20 mm in thickness, so it could be used in the next step of steelmaking and refining without any problems.

実施例2 実施例1と同様150を混銑車に受銑した溶銑(成分重
量%:C4,9B、Si O,51、Mn O,52、
PO,+05 、 So、044 、残Feならびに不
純物、溶銑温度1350°C)を前記第1容器を用いて
15t/分の速度で払い出し、フラックスとしてCaO
210kg/l−p+gを投入(一括投入)したところ
、払い出し後第2容器内溶銑(成分重量%:C4,8[
i、Si O,48、MnO,50、Po、100 、
  So、00? 、残Feならびに不純物、溶銑温度
1300°C)は、優れた脱硫効果を示した。
Example 2 Hot metal 150 was received in a pig iron mixing car as in Example 1 (component weight %: C4,9B, SiO,51, MnO,52,
PO, +05, So, 044, residual Fe and impurities, hot metal temperature 1350 ° C) were discharged at a rate of 15 t/min using the first container, and CaO was used as a flux.
When 210 kg/l-p+g was charged (in bulk), hot metal in the second container (component weight %: C4,8[
i, SiO, 48, MnO, 50, Po, 100,
So, 00? , residual Fe and impurities, hot metal temperature 1300°C) showed an excellent desulfurization effect.

実施例3 実施例2と同成分の溶銑(溶銑温度1410°C)を前
記第1容器へ10t1分の速度で払い出し、ミルスケー
ル23kg/l−pigを連続投入したところ、第2容
器内溶銑(成分重量%:C4,8?、Si O;07 
、 Mn0023、PO,O?’2 、S O,034
、残Feならびに不純物、溶銑温度1365°C)は優
れた脱珪効果を示した。
Example 3 Hot metal having the same composition as in Example 2 (hot metal temperature 1410°C) was discharged into the first container at a rate of 10 t/min, and a mill scale of 23 kg/l-pig was continuously introduced. Component weight %: C4,8?, SiO;07
, Mn0023, PO, O? '2, SO,034
, residual Fe and impurities, hot metal temperature 1365°C) showed an excellent desiliconization effect.

いずれの実施例の場合にも、これまでの溶銑払い出しに
比較して、第2容器内のスラグ量は半減し、又第1容器
内に残留したスラグは、容器のまま排滓ピットへ移動さ
せ排滓が容易であった。
In both examples, the amount of slag in the second container is halved compared to the conventional method of discharging hot metal, and the slag remaining in the first container is moved to the slag pit without leaving the container. It was easy to remove the slag.

又、比較例として、通常の多段にて、溶銑の予備処理を
行った場合をあげると、プロセスとして混銑車に受銑し
、混銑車内で脱硫後排滓、取鍋に溶銑を移して脱珪、排
滓、脱燐処理を行い、その後溶銑装入鍋への払い出しを
行ったとき、処理時間は、処理設備間の移動を含めない
場合でも、処理のみで1〜2時間を要し、最終処理温度
も処理時間に応じて低下する。
In addition, as a comparative example, let us consider the case where hot metal is pretreated in a normal multi-stage process.The process involves receiving the hot metal in a mixer car, desulfurizing it in the mixer car, removing the slag, and transferring the hot metal to a ladle to desiliconize it. When carrying out slag, dephosphorization treatment, and then discharging to the hot metal charging pot, the treatment time alone takes 1 to 2 hours, even if transportation between treatment facilities is not included, and the final The processing temperature also decreases depending on the processing time.

以上詳述したごとく本発明によれば、処理工程の簡略化
、処理時間の短縮、温度ロスの防止、転炉操業への負荷
低減等、トータル的な顕著な効果が得られる。
As described in detail above, according to the present invention, significant total effects such as simplification of treatment steps, reduction of treatment time, prevention of temperature loss, and reduction of load on converter operation can be obtained.

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

図面は本発明の一実施例を説明する立面図である。 1・・・容器、2・φ・第1容器、3・・・溶銑、3′
・・・溶銑落下流、4・・・精錬用フラックス、51 
@ @第2容器、6.6′・・・堰。 特許出願人 新日本製鐵株式會社
The drawing is an elevational view illustrating an embodiment of the present invention. 1... Container, 2, φ, first container, 3... Hot metal, 3'
... Falling flow of hot metal, 4 ... Flux for refining, 51
@ @Second container, 6.6'...Weir. Patent applicant Nippon Steel Corporation

Claims (1)

【特許請求の範囲】[Claims] 溶銑を第1容器へ払い出しつつ、第1容器内で落下溶銑
と精錬用フラックスとを接触せしめ、順次第2容器へ払
い出すことを特徴とする溶銑の予備処理力法。
A hot metal pretreatment method characterized in that while the hot metal is being discharged into a first container, the falling hot metal is brought into contact with a refining flux in the first container, and the hot metal is sequentially discharged into two containers.
JP6140783A 1983-04-07 1983-04-07 Pretreatment of molten iron Pending JPS59185715A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6140783A JPS59185715A (en) 1983-04-07 1983-04-07 Pretreatment of molten iron

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6140783A JPS59185715A (en) 1983-04-07 1983-04-07 Pretreatment of molten iron

Publications (1)

Publication Number Publication Date
JPS59185715A true JPS59185715A (en) 1984-10-22

Family

ID=13170240

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6140783A Pending JPS59185715A (en) 1983-04-07 1983-04-07 Pretreatment of molten iron

Country Status (1)

Country Link
JP (1) JPS59185715A (en)

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