JPS58151410A - Molten iron desiliconizing agent - Google Patents

Molten iron desiliconizing agent

Info

Publication number
JPS58151410A
JPS58151410A JP3438382A JP3438382A JPS58151410A JP S58151410 A JPS58151410 A JP S58151410A JP 3438382 A JP3438382 A JP 3438382A JP 3438382 A JP3438382 A JP 3438382A JP S58151410 A JPS58151410 A JP S58151410A
Authority
JP
Japan
Prior art keywords
slag
iron
desiliconization
hot metal
molten iron
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
JP3438382A
Other languages
Japanese (ja)
Other versions
JPS613364B2 (en
Inventor
Toshiyasu Onishi
大西 稔泰
Wataru Takagi
高木 彌
Tamotsu Yamaji
山地 保
Masahiko Ogami
大神 正彦
Junichiro Katsuta
勝田 順一郎
Hiroshi Matsumoto
洋 松本
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 JP3438382A priority Critical patent/JPS58151410A/en
Publication of JPS58151410A publication Critical patent/JPS58151410A/en
Publication of JPS613364B2 publication Critical patent/JPS613364B2/ja
Granted 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
    • C21C1/04Removing impurities other than carbon, phosphorus or sulfur

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 pretreat molten iron efficiently and simply by adding a specified amount of CaCO3 to scale or the like to obtain a molten iron desiliconizing agent having a specified grain size and by adding the agent to the molten iron during passing through an iron discharging spout. CONSTITUTION:At least 8-21wt% CaCO3 is added to an iron oxide-base material such as scale, ore or minus mesh from a sintering stage to obtain a molten iron desiliconizing agent composed of grains. All the grains have <=1.0mm. grain size, and grains having 0.1-1.0mm. grain size occupies >=50wt% of all the grains. Molten iron discharged from a blast furnace is desiliconized with the desiliconizing agent during passing through an iron discharging spout. Since slag formed by the desiliconization has high flowability, it can be removed easily through a slag discharging spout placed at the downstream side of the iron discharging spout.

Description

【発明の詳細な説明】 本発明は、高炉から出湯される溶銑を出銑樋通過中に脱
珪%塀する為の溶銑脱珪剤に関し、殊に脱珪効果が良好
で且つ排滓性の良い脱珪スラグを生成する脱11剤に関
するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a hot metal desiliconizing agent for removing silicon from hot metal tapped from a blast furnace while passing through a tap sluice, and particularly to a hot metal desiliconizing agent that has a good desiliconizing effect and a good slag removal property. This invention relates to a desiliconizing agent that produces good desiliconization slag.

高炉においてah!lされた溶銑には大量の#l!l1
1が會まれでいる為、これを酸化除去し、所定の温度K
N墨する目的で転炉等によるMm操業を行なっている。
In the blast furnace ah! There is a large amount of #l in the hot metal! l1
1 is present, so it is removed by oxidation and heated to a predetermined temperature K.
Mm operation using a converter, etc. is being carried out for the purpose of N ink.

しかし一般的な転炉@錬では、脱炭の他に脱燐等を目的
とすることが多く、その為大量の造滓剤を投入しCaO
糸箇基性スッスラよる脱燐#l錬をしてシシ、生成する
スラグの量1bX浴麟1トンm17104)−160k
gKも及ぶことがある。この様な製鋼スラグは言わば*
lI物であシ、再利用の方途が多方#Jにおいて検討さ
れているが、現時点でははは飽和伏線に達している。従
って用途開発技術の展開もさることながら、製鋼スラグ
の発生量を抑制することが基本的な解決手段であり、脱
燐中脱硫等を転炉N4#から切夛着して行ない。
However, in general converter@refining, the purpose is often to dephosphorize in addition to decarburization, and for that purpose, a large amount of slag-forming agent is input and the CaO
Amount of slag produced by 1 b x 1 ton of bath salt m 17104) - 160 k
gK may also be affected. This kind of steelmaking slag is so to speak *
Since it is an II product, many ways to reuse it are being considered in #J, but at present it has reached saturation. Therefore, in addition to the development of application development technology, the basic solution is to suppress the amount of steelmaking slag generated, and desulfurization during dephosphorization is carried out by cutting it from the converter N4#.

転炉精錬をもっばら脱炭と昇温目的に絞って行なうとい
う方向に切IOつつある。この様な精錬ではスラグの生
威量を減少することが可能であるだけでなく、スラグか
らの復燐や復硫という問題もなく*、a、又目標炭素量
の的中率が向上し、距には極低炭素鋼を製造することも
容易になるという利点がある。
There is a shift toward focusing converter refining exclusively on decarburization and temperature raising purposes. This kind of refining not only makes it possible to reduce the yield of slag, but also eliminates the problem of rephosphorization and resulfurization from slag*, and also improves the accuracy of the target carbon content. Steel has the advantage that it also makes it easier to produce ultra-low carbon steel.

以上の様な事情から、転炉等による精錬に先だって脱燐
等の予備処11(vhわゆる炉外精#)を行なうのが一
般的にな夛りつあるが、−Kに予備処増といっても脱珪
、脱燐、脱硫等があシ、これらの冶金反応には夫々異な
った最通の反応条件があってこれらを一括して行なうと
檀々の幣書があられれる0例えば脱珪反応によシ510
2が生成すると、脱燐剤や脱硫剤として添加されるCa
Oとの比(CaO/8402 )で示される塩基度が低
下し、脱燐中脱硫が不十分になる。そこでCaOを大量
に投入せざるを得なくなるが、このことはスラグ會の増
大につなか)、再び前述の関11に!遇する。この様な
ところから、脱珪を脱燐拳脱硫から切〉離し、溶銑をま
ず脱珪処理し要談脱珪スラグを除去し、次いで脱燐・脱
R処理を行なう方法4検討されている。しかしこの様な
方法では炉外精錬を複数回に分けて行なうので作業が煩
雑で且つ生産性が低く、W!KFi溶銑の温度がかなシ
低下するという問題があった。
Due to the above-mentioned circumstances, it is becoming more and more common to carry out preliminary treatment such as dephosphorization11 (vh so-called furnace refining) prior to refining in a converter, etc. However, there are still desiliconization, dephosphorization, desulfurization, etc. These metallurgical reactions each have different common reaction conditions, and if they are performed all at once, there will be a lot of trouble. Silica reaction 510
When 2 is generated, Ca added as a dephosphorizing agent or desulfurizing agent
The basicity indicated by the ratio to O (CaO/8402) decreases, and desulfurization during dephosphorization becomes insufficient. Therefore, we have no choice but to introduce a large amount of CaO, which leads to an increase in slag formation), which leads to the above-mentioned Seki 11 again! treat For this reason, a method is being considered in which desiliconization is separated from desulfurization and phosphorization, and hot metal is first subjected to desiliconization treatment to remove desiliconization slag, followed by dephosphorization and desulfurization treatment. However, in this method, the out-of-furnace refining is performed in multiple steps, which makes the work complicated and has low productivity. There was a problem in that the temperature of KFi hot metal decreased significantly.

本発明者等はこの様な伏動を憂慮し、溶銑の予備処理を
効率良く逐行することができる様な方法の開発が必要で
あると考えat々検討を1ねえ結果、溶銑を高炉から出
銑@経由で出湯する過程で脱珪を行なう様にすれば、予
備処理を簡略化し得るという感触を得た。即ち出銑樋経
由で出湯する道程にスキンマーを配置し、まず高炉スラ
グを分離する。次いで出銑樋中の浴銑に脱珪剤を添加し
溶銑樋通過中に脱珪を完了することによって、実質上の
脱珪設備及び脱珪時間を省略することが可能になる。こ
こで量線になるのは、上記の橡な言わば簡略法を採用し
た場合でも、溶銑中の珪素量を十分に低減し得る様にす
ることである。しかして第1図轢脱燐に及ぼす溶銑温度
と初期(SI)量の関係を示したものであるが、この図
からも明らかな様に溶銑中の(Si)量が多いと脱燐を
十分に行なうことができないので、事前の脱珪を十分に
行なうことが極めて重eKなる。tた今一つの間開は、
生成する脱珪スラグ層429の下流側で効率良く除去し
得る様にすることである。しかして脱珪スラグの除去が
不十分であると、前述の様に脱燐スラグの塩基度が低下
するという障害が現われ、壇え脱珪スラグの排滓樋等で
該スラグがS崖する様なことがあると、その後の脱着処
理自体が不可111になる。
The inventors of the present invention were concerned about such stagnation, and thought that it was necessary to develop a method that could efficiently carry out preliminary treatment of hot metal. I felt that the preliminary treatment could be simplified if desiliconization was performed during the process of tapping the iron via the tap. That is, a skinmer is placed in the path of tapping the tap water via the tap sluice, and first the blast furnace slag is separated. Next, by adding a desiliconizing agent to the bath pig iron in the tap runner and completing the desiliconization while the hot metal is passing through the tap runner, it becomes possible to substantially omit desiliconization equipment and desiliconization time. The purpose of determining the quantity line here is to ensure that the amount of silicon in the hot metal can be sufficiently reduced even when the above-mentioned simplistic method is adopted. However, Figure 1 shows the relationship between hot metal temperature and initial (SI) amount on road dephosphorization, and as is clear from this figure, when the amount of (Si) in hot metal is large, dephosphorization is Therefore, it is extremely important to perform sufficient desiliconization in advance. The only gap is
The purpose is to enable efficient removal of the generated desiliconization slag layer 429 on the downstream side. However, if the removal of the desiliconization slag is insufficient, the basicity of the dephosphorization slag will decrease as mentioned above, and the slag will form an S cliff in the slag drain of the desiliconization slag. If this happens, the subsequent attachment/detachment process itself becomes impossible 111.

本発−考等は上記の様な間蘭点の解消に着手し、浴銑樋
中を流下中の#銑を通用するだけでも高い脱珪効果を発
揮し、しか4流動性が良好で容易く排滓することができ
る様な脱珪スラグを生成すゐ様な脱珪剤を得ようとして
鋭意研究を進めてきた。
The present study has begun to solve the above-mentioned problems, and has shown that a high desiliconization effect can be achieved simply by passing ## pig iron flowing down through the bath pigtails. We have been conducting intensive research in an attempt to obtain a desiliconizing agent that can generate desiliconizing slag that can be removed.

木発崎はかかる研究の結果完成されたものであって、そ
の構成は、高炉から出湯される溶銑を出銑曽過過中に脱
珪処理する為の溶銑脱珪剤であって、スケール戚いは鉄
鉱石や燗結工程で発生する篩下など酸化鉄を主成分とす
る物質と共に少な(とも8〜21重量憾のC& C03
を含み、且つその粒Melt敗が0.1〜1.Offの
ものを50重量慢以上含むと共に全量が1.0W以下の
ものであるところに要旨が存在する。
Kibatazaki was completed as a result of such research, and its composition is a hot metal desiliconization agent for desiliconizing hot metal tapped from a blast furnace during the extraction process. In addition to iron ore and substances mainly composed of iron oxides, such as sifter generated in the sintering process, there are
and the grain melt loss is 0.1 to 1. The gist is that it contains 50% or more of the Off value and the total amount is 1.0W or less.

まず本発明では、脱珪剤としてスケ−Vと共KCaCO
3を使用するが、これを溶銑樋内の溶銑中に投入すると
、溶銑樋の落差部中曲p角で溶銑中に巻き込まれる。そ
して(1)、Cり式の反応によって浴銑中の5i−s@
化除去され廖−スラlを生成するが、caco3は#趨
と同時に熱分解を起こしてCO怠ガスを放めし、このガ
スは生成する脱珪スラグ層をつ自抜けて大気中へ逸出す
る。
First, in the present invention, KCaCO is used together with SCA-V as a desiliconizing agent.
3 is used, but when it is thrown into the hot metal in the hot metal gutter, it gets caught up in the hot metal at the curved p angle in the drop part of the hot metal gutter. And (1), 5i-s@ in the bath iron by C-type reaction
Caco3 undergoes thermal decomposition at the same time as #trend and releases CO gas, which passes through the desiliconization slag layer and escapes into the atmosphere. .

IF@g03+8($1)冨j18i0g+4F・  
1112FI110+(Sゑ)−8i02+2Fe  
  を組ところで脱珪スラグは生成′f&嬉銑溶銑に浮
上するが、l#aIM面で泡立ち杖霞を呈して見掛けの
流動性が低下し、さらにスラグ表Nll5が冷1jIJ
aW7Aシて下流側に分岐して設けた排滓樋からの排出
が困−になる。ところが脱珪剤としてCaCO3を含む
亀のを使用すると、前述の如くその溶融時に生成するC
O怠ガスが脱珪スラグ層をつき抜けるときに消泡効果が
発揮され、泡立ちが抑制される。その結果脱珪スラグの
流動性低下と表層部の摩剥凝固が抑制され、脱珪スラグ
の排滓性が高度に保持される。淘脱珪スラグのC807
810g比が低すVると融点及び粘性は上昇しF11I
!スッグの流動性が低下する。さもに前−述の様なCO
記ガスの発生による発泡抑制効果を有効に発揮させる為
には、少な(とも8重量憾以上のCaCO3を含有させ
なければならず、ま九C& C03量がS憾未満になる
と脱珪効果自体が乏しくなると共に、説曹ス雫グの塩基
度が小さくな)すぎて、浴銑中のMISがMltOとな
ってスラグ中に移行する量が多くなる1等の障害も生じ
て(る、一方chco3gが多す「ると、脱珪ス雫グO
塩基度が高くなって融点及び粘性が上昇すると共に%C
a CO30分解熱による温度低下、さらKは発生する
C0gガス量が過111になってスラグが冷却され、流
動性はかえって低下する。しかも脱珪剤の主成分である
スケ−A10X*比率が減少して脱珪効果が低下するの
で、(acO30含有率は21重會嘔以下に抑える必要
がある。ちなみに第2図cA)、 (1,(0は脱m削
中のcacos含有率を賛えた場合の生成スラグの排滓
性(排滓@におけるスラグO流動性)に与える影響を示
したグラフであシ、これらのグラフにもcaco3溢加
の有位性が和書Kliわれている。特に高炉から出湯さ
れる通常am銑に適冷する場合は、8〜911(DCa
CO3を會む脱珪剤を使用することによって排滓性を飛
躍的に高めることができる。tt4厳密な意味で0CI
CO3の最適含有率は溶銑中の(St)量と目櫂脱壇率
によって定めるのがよく、最も好ましいのは生成x 9
 FK)塩基qtd 0.8〜0.5とナル* K C
a CO3含有率を定めることである。
IF@g03+8 ($1) Tomi j18i0g+4F・
1112FI110+(Sゑ)-8i02+2Fe
By the way, the desiliconized slag rises to the surface of the generated hot metal, but it bubbles on the l#aIM surface and shows a haze, reducing the apparent fluidity.
aW7A, it becomes difficult to discharge the slag from the drainage gutter which is branched to the downstream side. However, when CaCO3 containing CaCO3 is used as a desiliconizing agent, as mentioned above, the C generated during melting is
When the O slag penetrates the desiliconization slag layer, an antifoaming effect is exerted and foaming is suppressed. As a result, a decrease in the fluidity of the desiliconized slag and abrasion solidification of the surface layer are suppressed, and the desiliconized slag maintains a high level of slag excretion. Desilicated slag C807
As the 810g ratio decreases, the melting point and viscosity increase and F11I
! The fluidity of sug decreases. Just like the above-mentioned CO
In order to effectively exhibit the effect of suppressing foaming due to the generation of the gas mentioned above, it is necessary to contain a small amount of CaCO3 (more than 8% by weight). At the same time, the basicity of the slag becomes too small, and the first problem occurs in which the amount of MIS in the bath iron becomes MltO and migrates into the slag. There are a lot of things, and then the drop of silica is removed.
As basicity increases, melting point and viscosity increase, and %C
a) The temperature decreases due to the heat of decomposition of CO30, and the amount of C0g gas generated exceeds 111, cooling the slag, and the fluidity decreases on the contrary. Moreover, since the SCA-A10X* ratio, which is the main component of the desiliconizing agent, decreases and the desiliconizing effect decreases, (the acO30 content must be kept below 21%. Incidentally, Figure 2 cA), ( 1, (0 is a graph showing the influence on the sludge drainage property (slag O fluidity in sludge @) when the cacos content rate during demolition is taken into account, and these graphs also The significance of caco3 overflow is described in Japanese books.Especially when cooling the normal AM pig iron discharged from the blast furnace, the
By using a desiliconizing agent that combines CO3, the sludge removal performance can be dramatically improved. tt4 0CI in the strict sense
The optimum content of CO3 is preferably determined by the amount of (St) in the hot metal and the removal rate of the main paddle, and the most preferable is the amount of CO3 generated x 9
FK) base qtd 0.8-0.5 and null* K C
a. Determine the CO3 content rate.

同螢石や氷晶石は各檀スラグの融点を降下させ流動性を
高めることが知られているが1本!!FM4においても
V&溶剤としてamの螢石や氷晶石を添加することは極
めて有効である。但し過11JK添加することは経済的
に無駄であシ、しかも溶解、反応fK有害な弗素が発生
するので、その含有率は6重量qII以下に抑える必要
がある。
Fluorite and cryolite are known to lower the melting point of each dan slag and increase its fluidity, but one! ! Also in FM4, it is extremely effective to add am fluorite or cryolite as a V&solvent. However, adding 11 JK is economically wasteful, and furthermore, fluorine, which is harmful to dissolved and reactive fK, is generated, so its content must be kept below 6 weight qII.

次に脱珪剤の粒度構成は良好な脱着率を得るのに極めて
重要である。即ち本発明では格別の脱珪炉を使用せず出
銑樋中で脱珪を行なうものであるから、tII樋中で溶
銑と効率良く接触度広する柵にしなければならず、その
為には脱珪剤の粒度#lIF!lが0.1〜1.0mの
ものを60重量−以上含むと共に全量が1.0■以下の
ものを使用する必要がある。
Next, the particle size structure of the desiliconizing agent is extremely important in obtaining a good desorption rate. That is, in the present invention, desiliconization is carried out in the tap trough without using a special desiliconization furnace, so the fence must be designed to efficiently widen the contact with the hot metal in the tII trough. Particle size of desiliconizing agent #lIF! It is necessary to use a material containing 60 weight or more of 1 to 1.0 m, and a total amount of 1.0 m or less.

しかして暫度が大きすぎると、脱珪剤が溶銑流の表面に
浮上するのみで深部まで巻込オれに((なシ、十分な脱
珪効果が得られな(なる。一方粒度の小さいものは、高
1の#銑の上方に形成される外式の対fItKよって飛
散し、脱珪剤のロスが多くなると共に、出fR樋オわ9
の作業雰囲気を著しく汚染する。ちなみに第8図は、脱
珪剤(成分組成は第1111)の粒度構成を櫨々餐史し
九場合の脱珪率に与える影豐を示したグラフ(原料溶銑
の(Si )含有率は0.1〜0.6優、脱珪剤添加量
はIIθ〜30kg/)ン)であシ、このグラフからも
明らかな様に、脱珪剤の粒径が1. Omを越えるもの
では脱珪率が低下している。ま走0.1 wx宋満の微
粒物を多量含むものでも脱珪率は着干低下しているが、
これは添加時の飛散により溶銑中への実質の添加量が減
少した為と考えられ、この場合添加付着周辺は飛散しえ
脱珪剤粉末によって着しく汚染されることが!!I認さ
れた。
However, if the grain size is too large, the desiliconizing agent only floats to the surface of the hot metal flow and becomes entangled deep inside the hot metal flow. The particles are scattered by the external pair fItK formed above the #1 pig iron, which increases the loss of desiliconizing agent and causes the flow of the outflow fR gutter.
seriously pollutes the working atmosphere. By the way, Figure 8 is a graph showing the influence of the particle size composition of a desiliconizing agent (composition is No. 1111) on the desiliconization rate in nine cases (the (Si) content of the raw hot metal is 0). .1 to 0.6, and the amount of desiliconizing agent added is IIθ to 30 kg/).As is clear from this graph, when the particle size of the desiliconizing agent is 1. If it exceeds Om, the desiliconization rate decreases. The desiliconization rate is decreasing even in the case of 0.1 wx Songman containing a large amount of fine particles, but
This is thought to be due to the fact that the actual amount added to the hot metal decreased due to scattering during addition, and in this case, the area around the addition adhesion could be heavily contaminated by the scattering desiliconizing agent powder! ! I was approved.

@1表 1況珪剤の成分組Fit(電量憾)本発明は概
略以上の様に構成されてシ〉、脱珪剤中のCaO成分と
して適量のcaco3を含有せしめると共に粒度構成を
遍正に調整することKよって、出銑樋を流れる過程で効
率良く脱珪処理することができる1aKなつ九。しかも
生成する脱珪スラグは流動性が良好であるから、樋の下
流備に設けえ排滓樋から容易に除去することがで自、処
m博銑への脱珪スラグの混入量を可及的に少な(するこ
とができる。その結果、脱珪処#炉等の設置及び脱珪処
理時間を実質的に省略することができ、予備処理の設備
及び操作を簡略化し得ると共に予備処理効率を高め得る
ことに1につた。
@1 Table 1 Situation Composition of Silicant Fit (Amount of Electricity) The present invention is roughly constructed as described above.In addition to containing an appropriate amount of caco3 as the CaO component in the desiliconizing agent, the particle size structure is made uniform. By adjusting K, it is possible to efficiently remove silicon in the process of flowing through the tap pipe. Moreover, the generated desiliconization slag has good fluidity, so it can be installed in the downstream equipment of the gutter and easily removed from the slag drainage gutter, thereby reducing the amount of desiliconization slag mixed into the pig iron in the process. As a result, the installation of a desiliconization furnace, etc. and the desiliconization treatment time can be substantially omitted, and the pretreatment equipment and operation can be simplified, and the pretreatment efficiency can be increased. To my delight, it reached number 1.

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

第1図は脱燐に及ぼす溶銑tjAM及び初期〔si〕の
影響を示すグラフ、Il!2図(4)、(至)、(Qは
脱珪剤中0CaCO3含有率と排滓性の関係を示すグラ
フμ5FIIJは脱珪剤の粒度構成と脱珪率の関係を示
すグラフである。 出願人  株式会社神戸製鋼所 珪 脱CP)処理前の溶銑<Sr>量(X10%)重石灰石
無添加   炭酸カルシウム添加  炭酸カルシウム添
加(10〜21%)    (3〜10%未満)第3図 溶銑(Si)C%) 手続補正書C方式】 %式% 1、事件の表示 昭和sr  年 特 許 願第 114188 号昭和
   年   、    第      号2、発明又
は考案の名称 濤銑説醜剤 3、補正をする者 事件との関係     特 許出願人 住 所  神戸市中央区脇浜町−丁目3番18号4、代
  理  人  郵便番号530住 所  大阪市北区
堂島二丁目3番7号 シンコービル電話大阪(06) 
343−2325 (代)6、補正の対象 (1)明細書第7夏第6行O「ダツツであ襲、」t「ダ
ツツ(118図(4)嬬石訳石無添加、岡(2)拡鰐酸
力A/Vつふ1G−1111添加、岡ロ拡炭酸★fi/
Vウム8〜101未満〕であ〉、」と訂正します。 (動第鵞1a(A) 、 @ 、ロ會別紙i違ヤ訂正し
ます。 第2図 (A)          (B) 排滓性      排滓性 (C) 悪普良 通 排滓性
Figure 1 is a graph showing the influence of hot metal tjAM and initial [si] on dephosphorization, Il! Figure 2 (4), (to), (Q is a graph showing the relationship between the CaCO3 content in the desiliconizing agent and slag removal performance μ5 FIIJ is a graph showing the relationship between the particle size structure of the desiliconizing agent and the desiliconizing rate. Application People Kobe Steel Co., Ltd. Silicification CP) Amount of hot metal <Sr> before treatment (X10%) No addition of heavy limestone Addition of calcium carbonate Addition of calcium carbonate (10 to 21%) (Less than 3 to 10%) Figure 3 Hot metal ( Si)C%) Procedural amendment C method]% formula% 1. Indication of the case Showa Sr. Patent Application No. 114188 Showa No. 2. Name of the invention or device 3. Make an amendment Relationship with the patent applicant case Address: 3-18-4 Wakihama-cho, Chuo-ku, Kobe City Agent: Zip code 530 Address: 2-3-7 Dojima, Kita-ku, Osaka Shinko Building Telephone Osaka (06) )
343-2325 (generation) 6, subject of amendment (1) Specification, 7th summer, line 6 O “Datsutsu de attack,” t “Datsutsu (Figure 118 (4) Tsumuishi translation without addition of stone, Oka (2) Expanded Acid Power A/V Tsufu 1G-1111 added, Okaro Expanded Carbonated★fi/
Vum 8-101〉〉,'' I corrected it. (Movement number 1a (A), @, I will correct the difference in the attached sheet. Figure 2 (A) (B) Sludge drainage performance Sludge drainage performance (C) Bad, normal, and good sludge drainage performance

Claims (1)

【特許請求の範囲】 口)高炉から出湯される溶銑を出銑樋通過中に脱珪処理
する為の溶銑脱珪剤であって、スケール。 鹸鉱石、焼結鉱篩下尋0@化鉄と共に少なくとも8〜2
1重量嘔のcaco3を含み、且つその粒度構5!′b
Xo、t〜1.01のものを50重量憾以上含むと共に
全量が1.01以下のものであることを特徴とする溶銑
脱珪剤。
[Scope of Claim] Mouth) A molten pig iron desiliconization agent for desiliconizing hot metal tapped from a blast furnace while passing through a tap culvert, and a scale. Saponite, sintered ore under sieve 0 @ at least 8 to 2 with iron oxide
Contains 1 weight of caco3, and its particle size is 5! 'b
A desiliconizing agent for hot metal, characterized in that it contains 50 weight or more of Xo, t~1.01, and the total amount is 1.01 or less.
JP3438382A 1982-03-03 1982-03-03 Molten iron desiliconizing agent Granted JPS58151410A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3438382A JPS58151410A (en) 1982-03-03 1982-03-03 Molten iron desiliconizing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3438382A JPS58151410A (en) 1982-03-03 1982-03-03 Molten iron desiliconizing agent

Publications (2)

Publication Number Publication Date
JPS58151410A true JPS58151410A (en) 1983-09-08
JPS613364B2 JPS613364B2 (en) 1986-01-31

Family

ID=12412642

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3438382A Granted JPS58151410A (en) 1982-03-03 1982-03-03 Molten iron desiliconizing agent

Country Status (1)

Country Link
JP (1) JPS58151410A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62247015A (en) * 1986-04-21 1987-10-28 Kawasaki Steel Corp Desiliconizing agent for molten iron
KR20010100203A (en) * 2000-03-16 2001-11-14 이구택 A desiliconizer for molton pig iron

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56217A (en) * 1979-06-14 1981-01-06 Nippon Steel Corp Continuous desilicification for molten pig iron

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56217A (en) * 1979-06-14 1981-01-06 Nippon Steel Corp Continuous desilicification for molten pig iron

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62247015A (en) * 1986-04-21 1987-10-28 Kawasaki Steel Corp Desiliconizing agent for molten iron
KR20010100203A (en) * 2000-03-16 2001-11-14 이구택 A desiliconizer for molton pig iron

Also Published As

Publication number Publication date
JPS613364B2 (en) 1986-01-31

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