JPS58153717A - Flux for refining and its using method - Google Patents

Flux for refining and its using method

Info

Publication number
JPS58153717A
JPS58153717A JP3619682A JP3619682A JPS58153717A JP S58153717 A JPS58153717 A JP S58153717A JP 3619682 A JP3619682 A JP 3619682A JP 3619682 A JP3619682 A JP 3619682A JP S58153717 A JPS58153717 A JP S58153717A
Authority
JP
Japan
Prior art keywords
hot metal
flux
ash
dephosphorization
desulfurization
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
JP3619682A
Other languages
Japanese (ja)
Other versions
JPS6127442B2 (en
Inventor
Isao Tozawa
戸沢 勇雄
Shinobu Hoshijima
星島 忍
Sadami Myonaka
妙中 定実
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.)
RIKEN KOGYO KK
TAENAKA KOGYO KK
Tanaka Kogyo Co Ltd
Original Assignee
RIKEN KOGYO KK
TAENAKA KOGYO KK
Tanaka Kogyo Co 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 RIKEN KOGYO KK, TAENAKA KOGYO KK, Tanaka Kogyo Co Ltd filed Critical RIKEN KOGYO KK
Priority to JP3619682A priority Critical patent/JPS58153717A/en
Publication of JPS58153717A publication Critical patent/JPS58153717A/en
Publication of JPS6127442B2 publication Critical patent/JPS6127442B2/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
    • C21C1/02Dephosphorising or desulfurising
    • C21C1/025Agents used for dephosphorising or desulfurising

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 economically profitably carry out the dephosphorization and desulfurization of hot metal, by a method wherein flux obtained at a low cost is used by feeding the flux having burnt trona ash as main component into hot metal at a certain rate and by mixing them. CONSTITUTION:The dephosphorization and desulfurization is carried out by feeding the flux having the trona ash burnt at a low temperature as main component of 10-20kg per 1ton of hot metal into hot metal and by mixing them. For the method of feeding this flux, the abovementioned flux is injected into the hot metal in a mixer car or an iron ladle together with inert gas such as N2, Ar, etc., or is fed during stirring hot metal with an impeller. Thereby, hot metal is caused to react with the flux, and the reactions of desulfurization and dephosphorization of hot metal are made to proceed at the same time. This method has plenty of economical merit because of using cheaper trona ash as raw materials by comparing the beforehand known refining method using extremely highly refined soda ash. That is, the decrease of cost may be obtained, for example, by not less than 30%.

Description

【発明の詳細な説明】 本発明は、溶銑の脱燐・脱硫処理工程で用いる精錬用媒
溶剤及びその使用方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a refining solvent used in the dephosphorization/desulfurization process of hot metal and a method for using the same.

高炉から出銑される溶銑中に含有される燐分及び硫黄分
は、鋼の品質を劣化させる原因となるので除去か必要で
あり、4襲こ出銑後に混銑車なとにおいてその除去処理
が行われている。
Phosphorus and sulfur contained in the hot metal tapped from the blast furnace need to be removed because they cause deterioration of the quality of steel. It is being done.

近年、アルカリ金属炭酪勇を主成分とする媒溶剤、例え
ばソーダ灰に蛍石、コレスナイト、酸化鉄等の酸化剤を
混入した媒溶剤を溶銑中に壮大して脱燐・脱硫を行うこ
とが試みられており、その効果も顕著であることが認め
られている。この方法によれは、脱燐・脱硫剤の使用敏
が従来の他の脱燐・脱硫方法に比較して少なく、例えば
ソーダ灰は溶銑のI・ン当り、10〜20Kgで済むこ
とになる。特に脱燐1−程が効率良く進行し、流動性の
良好な鉱滓が得られるために、鉱滓中の粒鉄含イ1吊−
も非常に少ないという大きな利点を有するものとなり、
更には発生する鉱滓量も少ないので鉱滓の処理が簡便と
なる。
In recent years, it has become possible to dephosphorize and desulfurize hot metal using a solvent whose main component is alkali metal charcoal, for example, soda ash mixed with an oxidizing agent such as fluorite, cholestonite, or iron oxide. It has been tried, and its effects have been found to be significant. According to this method, the usability of the dephosphorization/desulfurization agent is less than that of other conventional dephosphorization/desulfurization methods; for example, 10 to 20 kg of soda ash is required per unit of hot metal. In particular, since the dephosphorization process progresses efficiently and slag with good fluidity is obtained, the granular iron content in the slag is
It has the great advantage that there are very few
Furthermore, since the amount of slag generated is small, the slag can be easily disposed of.

このように、l−述の脱燐・脱硫方法は注目されている
精錬法であるが、ここでの大きな障害は主剤であるソー
ダ灰が高価につくことである。ソーダ灰は従来、硝子工
業、窯業、化学薬品王楽においてその殆どが消費yれて
いたために、精製にょリ1業薬品としての高純度を有し
ており、価格か高いものとなっている。このソーダ灰は
例えば下記の分析値の通り、製鉄業で必要とする以上の
純度の旨いものが使用されているのである。
As described above, the dephosphorization/desulfurization method mentioned above is a refining method that is attracting attention, but the major obstacle here is that the main ingredient, soda ash, is expensive. Traditionally, soda ash has been mostly consumed in the glass industry, ceramic industry, and chemical industry, so it has a high purity and is expensive as a refining industrial chemical. For example, as shown in the analysis below, this soda ash has a purity higher than that required by the steel industry.

N a 2 CO:s    98 、5−99 、 
O%NaC,G       O,5% S04       0.1% FeOO,006% NaOHO,2% NaHCO30,2% 本発明の目的は、溶銑の精錬工程ではこのような高純度
の1業薬品に類するものを敢えて使用する必要がないこ
とに着目し、価格的に安価に得られる精錬用媒溶剤を提
供することにある。本発明の他の[]的は、1−述の媒
溶剤を効果的に使用する精錬用媒溶剤の使用方法を提供
することにある。
Na2CO:s98, 5-99,
O%NaC,G O,5% S04 0.1% FeOO, 006% NaOHO, 2% NaHCO30.2% The purpose of the present invention is to avoid using chemicals similar to these high-purity first-class chemicals in the hot metal refining process. The object of the present invention is to provide a refining solvent that can be obtained at a low price, paying attention to the fact that it is not necessary to use it. Another object of the present invention is to provide a method for using a refining solvent that effectively uses the solvent described in 1-1.

1−述の目的を達成するための采発明の要旨は、焼成し
たトロナ灰を主成分とすることを特徴とする精錬用媒溶
剤である。
1--To achieve the above-mentioned object The gist of the invention is a refining solvent characterized in that the main component is calcined trona ash.

また、前記発明に関連する本発明の要旨は、溶銑中に、
低温焼成したトロナ灰を−1:成分とする17M溶剤を
、溶銑1トン当り、10〜20Kg投入、)W拌して、
溶銑の脱燐・脱硫を行うことを特徴とする精錬用媒溶剤
の使用方法である。
Moreover, the gist of the present invention related to the above-mentioned invention is that in hot metal,
10 to 20 kg of a 17M solvent containing low-temperature fired trona ash as a component is added per ton of hot metal, and stirred with W.
This is a method of using a refining solvent, which is characterized by dephosphorizing and desulfurizing hot metal.

ここでトロナ灰とは天然に産する錆、物であり、その組
成4分は産地によっても異なるか、代表的な数伯例を挙
げれば次の通りである。
Here, trona ash is a naturally occurring rust substance, and its composition varies depending on the place of production, and some typical examples are as follows.

例l NaHCO3・2H2050,7% N a HCO344、4% NaCl1l         t、o%NaF   
      l 、28%CaCO30,25% 5i02        2.01% 例2 NaHCO3,、、、e2H2066,7%、1 NaHCO329,0% NaCN         O,9% NaF          1.19%CaCO30,
21% 5i07               1.70%例
3 Na2 co3     45.2% NaHCO,,35,7% NaF          O,9% Na2S0.      0.1% 結晶水         15.3% これらのトロナ灰を例えば120〜130℃で低温焼成
すると、例えは、 Na2CO397,4〜98.2% NaCρ   1.63〜0.32% NaF     0.22−0.30%程爪となり、そ
れ以外の成分N a HCOA。
Example l NaHCO3.2H2050,7% Na HCO344,4% NaCl1l t, o%NaF
l , 28%CaCO30,25% 5i02 2.01% Example 2 NaHCO3,,,e2H2066,7%,1 NaHCO329,0% NaCN O,9% NaF 1.19%CaCO30,
21% 5i07 1.70%Example 3 Na2 co3 45.2% NaHCO, 35.7% NaFO, 9% Na2S0. 0.1% Water of crystallization 15.3% When these trona ash are calcined at a low temperature of 120 to 130°C, for example, Na2CO397,4 to 98.2% NaCρ 1.63 to 0.32% NaF 0.22- Approximately 0.30% becomes nails, and the other ingredients are Na HCOA.

Na2 S04等は1%程度又はそれ以下となる。Na2, S04, etc. are about 1% or less.

この焼成によりトロナ灰中の付着水、結晶水が蒸発する
と共に、NaHCO3の水分か無くなり、Na2 co
、に変えられるのである。なお、焼成湿度は1−述のよ
うに比較的低温か好適であるが、他の湿度、例えば大嵯
に工業的に生Ieするためには高調で焼成しても支障は
ない。
This calcination evaporates the adhering water and crystallized water in the trona ash, and also eliminates the moisture in NaHCO3, converting Na2 co
, it can be changed to . It is preferable that the firing humidity is relatively low as described in 1-1, but there is no problem in firing at a higher humidity for industrial production at other humidity, for example, Oosaka.

このI・ロナ次を焼成した媒溶剤を、11N銑市中、或
いは溶銑鍋中の溶銑内に、窒素、アルゴン等の不活性カ
スと共に吹き込むとか、または溶銑をインペラで攪拌し
ながら投入することにより、溶銑と媒溶剤とを反応させ
と、溶銑の脱燐・脱硫反応が同時に進行することになる
By blowing the solvent obtained by firing this I-ronaji into the 11N pig iron market or into the hot metal in a hot metal pot together with inert residues such as nitrogen and argon, or by adding the hot metal while stirring it with an impeller. When the hot metal and the solvent are reacted, the dephosphorization and desulfurization reactions of the hot metal proceed simultaneously.

例えば脱燐反応は。For example, the dephosphorization reaction.

(415)[P コ + Na2COA−(N a2o
)+  (215)(P2o、、)+Cの反応機構で表
される。
(415) [P co + Na2COA−(N a2o
)+ (215)(P2o, , )+C is represented by the reaction mechanism.

また、このようにして生成された媒溶剤中には、Na2
 SO2、NaF、NaCρ等のハロゲン化合物も含有
されており、これらの化合物は鉱滓の凝固温度を低重さ
せるなどの好結果をもたらすことになる。特に、ソーダ
灰にはNaFは含有されておらず、NaFから成る蛍石
をわざわざ添加しているのが現状である。しかしトロナ
灰中にはNaFが含まれているために、蛍石の使用原単
位が低ドし非富に有効である。
In addition, the solvent produced in this way contains Na2
It also contains halogen compounds such as SO2, NaF, and NaCρ, and these compounds bring about favorable results such as lowering the solidification temperature of the slag. In particular, soda ash does not contain NaF, and at present, fluorite, which is made of NaF, is intentionally added. However, since trona ash contains NaF, the unit consumption of fluorite is low, making it effective for non-rich ash.

この場合、媒溶剤は例えば200pm程廉の粒用として
用いることか好適である。媒溶剤としての1−は#銑1
トン当り、10〜20Kg程+Wで1−分な脱燐・脱硫
を行う性能をイラしていることが確8だされており、得
られる鉱滓の性状も良好である。
In this case, it is preferable to use the solvent for particles with a particle diameter of about 200 pm, for example. 1- as a solvent is #pig 1
It has been confirmed that the performance of dephosphorization and desulfurization for 1 minute with 10 to 20 kg of +W per ton is poor, and the properties of the obtained slag are also good.

史には純度の高いソーダ灰に比較して、例えは吸湿性が
少ないなど取扱いも容易である。
Historically, it is easier to handle than soda ash, which has a high purity and is less hygroscopic.

また、例えば酸化鉄、マンガン、クロム、ニッケル、バ
ナジウム、ニオブ、リチウム等の酸化物を、このりy、
溶剤に1種類又は2種類以トを若干早41配合すると更
にその効果は顕著である。
In addition, for example, oxides such as iron oxide, manganese, chromium, nickel, vanadium, niobium, lithium, etc.
The effect is even more remarkable when one or more of these are added to the solvent a little earlier.

以1−説明したように本発明に係る精錬用奴溶剤及びそ
の使用ブラ法は、従来知られている極めて高度に精製さ
れたソーダ灰、及びソーダ灰を使用する精錬法に比較し
、安価なトロナ灰を原料としているので、経済的な利点
が大きく、例えば30%以1−もコストが低下すること
になり、実際の操業トもソーダ灰を使用する場合と殆ど
回しであ73−
As explained in 1-1 above, the refining slave solvent and the method using the same according to the present invention are cheaper than the conventionally known extremely highly refined soda ash and the refining method using soda ash. Since trona ash is used as a raw material, it has great economic advantages, for example, costs can be reduced by 30% or more, and the actual operating costs are almost the same as when using soda ash.

Claims (1)

【特許請求の範囲】 ■、焼成したトロナ灰を主成分とすることを特徴とする
精練用媒溶剤。 2、溶銑中に、焼成したトロナ灰を主成分とする媒溶剤
を、溶銑1トン当り、10〜20Kg投入、攪拌して、
溶銑の脱燐・脱硫を行うことを特徴とする精錬用媒溶剤
の使用方法。 3、前記媒溶剤に酸化物を加えて溶銑中に投入、攪拌す
る特許請求の範囲第2項記載の精錬用媒溶剤の使用方法
[Scope of Claims] (1) A scouring solvent characterized in that the main component is calcined trona ash. 2. Add 10 to 20 kg of a solvent mainly composed of calcined trona ash into the hot metal and stir it,
A method of using a refining solvent characterized by dephosphorizing and desulfurizing hot metal. 3. The method of using a refining solvent as set forth in claim 2, which comprises adding an oxide to the solvent and adding it into hot metal and stirring.
JP3619682A 1982-03-08 1982-03-08 Flux for refining and its using method Granted JPS58153717A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3619682A JPS58153717A (en) 1982-03-08 1982-03-08 Flux for refining and its using method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3619682A JPS58153717A (en) 1982-03-08 1982-03-08 Flux for refining and its using method

Publications (2)

Publication Number Publication Date
JPS58153717A true JPS58153717A (en) 1983-09-12
JPS6127442B2 JPS6127442B2 (en) 1986-06-25

Family

ID=12462970

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3619682A Granted JPS58153717A (en) 1982-03-08 1982-03-08 Flux for refining and its using method

Country Status (1)

Country Link
JP (1) JPS58153717A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5265963A (en) * 1991-05-13 1993-11-30 Thk Co., Ltd. Side cover fixing structure for linear motion bearing

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5265963A (en) * 1991-05-13 1993-11-30 Thk Co., Ltd. Side cover fixing structure for linear motion bearing

Also Published As

Publication number Publication date
JPS6127442B2 (en) 1986-06-25

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