JPS602611A - Desiliconizing agent mixed with light burned dolomite for treating molten iron - Google Patents

Desiliconizing agent mixed with light burned dolomite for treating molten iron

Info

Publication number
JPS602611A
JPS602611A JP10917983A JP10917983A JPS602611A JP S602611 A JPS602611 A JP S602611A JP 10917983 A JP10917983 A JP 10917983A JP 10917983 A JP10917983 A JP 10917983A JP S602611 A JPS602611 A JP S602611A
Authority
JP
Japan
Prior art keywords
slag
desiliconization
molten iron
agent
dust
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
JP10917983A
Other languages
Japanese (ja)
Inventor
Toshinori Minagawa
皆川 俊則
Kenichi Kaneko
憲一 金子
Kazuo Okumura
奥村 和男
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 JP10917983A priority Critical patent/JPS602611A/en
Publication of JPS602611A publication Critical patent/JPS602611A/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
    • 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 obtain the titled desiliconizing agent consisting of iron oxide dust such as converter dust and light burned dolomite, enabling the efficient desiliconization of molten iron, and preventing resulfurization during desiliconization. CONSTITUTION:Iron oxide dust such as converter dust is mixed with light burned dolomite to prepare a desiliconizing agent 8. This agent 8 is put in a molten iron trough 4 from a hopper 7. Slag having low viscosity and a significant slag making effect is formed with the agent 8, and molten iron is efficiently desiliconized while effectively preventing resulfurization. At the same time, desulfurization is carried out.

Description

【発明の詳細な説明】 本発明は、溶銑の処理剤に詠り、詳細には、溶銑の脱珪
を効率的に達成でき、併わせて脱珪時の復硫を防止し得
る溶銑処理用脱珪剤に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a treatment agent for hot metal, and more specifically, to a treatment agent for hot metal that can efficiently desiliconize hot metal and prevent resulfurization during desiliconization. Regarding desiliconizing agents.

溶銑の脱珪処理に関しては、溶銑に酸化鉄系の焼結鉱、
ダスト等を添加する方法が従来より知られている。
Regarding the desiliconization treatment of hot metal, iron oxide-based sintered ore is added to the hot metal.
A method of adding dust or the like is conventionally known.

しかし、この方法の場合、脱珪処理時に脱珪スラグの塩
基度(Oak/Sin、 )が著しく低下しく0〜00
a)、これがトピードまたは溶銑鍋の内面に付着してい
る脱硫スラグと反応してS濃度が者しく高いスラグを形
成するため、溶銑中のSがスラグ−溶銑反応によって著
しく上昇し、製鋼工程における脱珪処理後の工程に大き
な支障をきたしていた。
However, in the case of this method, the basicity (Oak/Sin, ) of the desiliconized slag decreases significantly during desiliconization treatment, and
a) This reacts with the desulfurization slag adhering to the inner surface of the torpedo or hot metal ladle to form slag with a significantly high S concentration, resulting in a significant increase in S in the hot metal due to the slag-hot metal reaction, resulting in This was causing a major hindrance to the process after desiliconization.

この対処手段として、石灰を塩基度調整剤として用いる
方法も考えられるが、この方法であっても、石灰を多量
に添加した場合には、脱珪スラグの粘度が著しく上昇す
るので、滓化せず、脱硫能を殆んど有しないという欠点
がある。
One way to deal with this problem is to use lime as a basicity regulator, but even with this method, if a large amount of lime is added, the viscosity of the desiliconized slag will increase significantly, so it will not turn into slag. First, it has the disadvantage of having almost no desulfurization ability.

そこで、本発明者等は、これらの欠点を解消し、粘度が
低い脱珪スラグを形成し得ると共に脱珪時に復硫を防止
し得る脱珪剤を開発するべく鋭意研究した結果、塩基度
調整剤として軽焼ドロマイト号添加することによって極
めて効果的に脱珪・脱硫同時処理が可能となることを見
い出したのであるO 即ち、本発明の脱珪剤は酸化鉄系ダストに軽焼ドロマイ
トを混合せしめたことを特徴とTるものである。
Therefore, the present inventors conducted extensive research to eliminate these drawbacks, form a desiliconizing slag with low viscosity, and prevent resulfurization during desiliconization. It has been discovered that by adding light calcined dolomite as an agent, simultaneous desiliconization and desulfurization can be carried out extremely effectively. It is characterized by the fact that it was made possible.

以下、本発明について詳細に説明する。The present invention will be explained in detail below.

脱珪用ダストとしては、酸化鉄系のものであれば適宜の
ものを使用することができるが、スラグ発生を可能な限
り防止するうえで、できるだけ酸化鉄分の多いダストが
好ましく、この点を考慮すると、転炉ダストは、 (i)コストが安く、ダスト処理費用も軽減でき、(i
i)酸化鉄分が70〜90%と高含有率で含まれている
、 等の理由から、好適である。転炉ダストの成分例を表−
1に示す。
Any suitable iron oxide-based dust can be used as the desiliconizing dust, but in order to prevent slag generation as much as possible, it is preferable to use dust with as much iron oxide as possible, and this point should be taken into account. Then, converter dust is (i) inexpensive, reduces dust treatment costs, and (i)
i) Contains iron oxide at a high content of 70 to 90%, and is therefore suitable. Table shows examples of components of converter dust.
Shown in 1.

なお、酸化鉄分が70%より少ない含有量のものである
と、スラグの発生量のみが増加し、脱珪効率が低下Tる
ので、望ましくない。
In addition, if the iron oxide content is less than 70%, only the amount of slag generated increases and the desiliconization efficiency decreases, which is not desirable.

塩基度調整剤として軽焼ドロマイトを使用する、のけ、
後述の各種実験例の分析結果より、(i)石灰を使用し
た場合に比べて、脱珪スラグの粘度ご著しく低くでき、
滓化性が良好である、(ii) OaO及びMgOの含
有率が各々概ね60チ及び80%であるので塩基度が高
く、石灰系に比べても、十分な脱硫能を期待できる、 等のためである。軽焼ドロマイトの成分例を表−2に示
す。
Noke using lightly calcined dolomite as a basicity regulator,
From the analysis results of various experimental examples described below, (i) the viscosity of desiliconized slag can be significantly lowered compared to when lime is used;
(ii) The content of OaO and MgO is approximately 60% and 80%, respectively, so the basicity is high, and even compared to lime-based materials, sufficient desulfurization ability can be expected. It's for a reason. Table 2 shows examples of the components of light calcined dolomite.

表−2(係) なお、ドロマイト(xgco8)は% CO2源を有踵
吸熱反応により溶銑温度分低下させる等のため、塩基度
調整剤として好ましくない。
Table 2 (Part 2) Note that dolomite (xgco8) is not preferred as a basicity regulator because it lowers the CO2 source by the amount of hot metal temperature due to an endothermic reaction.

本発明の如く、塩基度調整剤として軽焼ドロマイ)’I
F−使用すると、従来の如く石灰を使用した場合に比べ
て、脱珪スラグの滓化性が有利であり、これは本発明者
等の実験によって判明した。即ち、一般に、脱硫能は以
下の式で表わされる。
As in the present invention, lightly calcined dolomite)'I as a basicity regulator
When F- is used, the desiliconizing slag has better slagability than when lime is used as in the past, and this has been found through experiments by the present inventors. That is, desulfurization ability is generally expressed by the following formula.

但し、(S):溶滓中のS濃度 〔S〕:溶銑中のS濃度 Os:サルファイトキャパシティ Po2:酸素分圧(atm) T :温度(℃) log Os −−5,54+ 1.;15 A ・・
・・・・・・・・・・・・・(2)OaO 以上の式かられかるように、Aca。(即ち、サルファ
イドキャパシティ)が高いほど、脱硫が有利である。こ
の点、(8)式の関係からして、化学反応的には(%a
aO)と(%MgO)の・函数の差だけ石灰の方が有利
ではあるが、物理的には脱珪スラグの滓化状況(粘度)
が問題となり、石灰系と軽焼ドロマイトのどちらが有利
かを解明するため、次の実験を行い検討した。
However, (S): S concentration in slag [S]: S concentration in hot metal Os: Sulfite capacity Po2: Oxygen partial pressure (atm) T: Temperature (°C) log Os −-5,54+ 1. ;15 A...
・・・・・・・・・・・・・・・(2) OaO As can be seen from the above formula, Aca. The higher the sulfide capacity (ie, sulfide capacity), the more advantageous is desulfurization. In this respect, from the relationship of equation (8), in terms of chemical reaction, (%a
Lime is advantageous due to the difference in function between aO) and (%MgO), but physically, the slag status (viscosity) of desiliconization slag
was a problem, and the following experiment was conducted to find out which is more advantageous: lime-based or lightly calcined dolomite.

即ち、脱珪剤左して、転炉ダスト20J19/l−pと
軽焼ドロマイ)101119/l−pの混合物(a)及
び転炉ダスト20”9/l−pと石灰10 kg / 
t−pの混合物(b)の2種類を準備して溶銑中に添加
し、脱珪反応によって溶銑中のS土を0.40%→0.
10%に低下させた時の各々のスラグ組成を分析した。
That is, as a desiliconizing agent, a mixture (a) of converter dust 20J19/l-p and light calcined dolomite) 101119/l-p, converter dust 20''9/l-p and lime 10 kg/
Two kinds of mixtures (b) of t-p were prepared and added to hot metal, and the S soil in the hot metal was changed from 0.40% to 0.0% by desiliconization reaction.
The composition of each slag was analyzed when it was reduced to 10%.

その(4) 結果ご第1図に示T。Part (4) The results are shown in Figure 1.

同図は、OaO−MgO−5in2(7)等粘度線(1
500°C,poise、(I、I、 Cu1t’ y
ai G: Jニル) ) ノ三角ダイヤグラムの一部
な表わしたもので、スラグ組成は計算上のものである。
The figure shows the OaO-MgO-5in2(7) isoviscosity line (1
500°C, poise, (I, I, Cu1t' y
This is a partial representation of the triangular diagram, and the slag composition is calculated.

図かられかるように、混合物(a)を使用したスラグの
MgOは20%でスラグ粘度約a poiseであるの
に対し、 MgOを含んでいない混合物(b)を使用し
た場合のスラグ粘度は50 poiseを超えている0
したがって、スラグ滓化状況については、 MgOを含
有する軽焼ドロマイトを使用した場合の方が著しく有利
である0 (実施例) 脱珪剤として、転炉ダストのみからなるもの。
As can be seen from the figure, the MgO content of the slag using mixture (a) is 20% and the slag viscosity is about a poise, whereas the slag viscosity when using the mixture (b) which does not contain MgO is 50%. 0 exceeding poise
Therefore, in terms of slag slag formation, it is significantly more advantageous to use lightly calcined dolomite containing MgO.0 (Example) A desiliconization agent consisting only of converter dust.

転炉ダスト8に対し石灰1の割合で混合したもの並びに
転炉ダストに各種割合で軽焼ドロマイトを混合したもの
の8種類を準備し、第2図の脱珪フローに示すように、
これらの脱珪剤8を4000m°級高炉1でホッパー7
より溶銑枝樋4に投入する方法で脱珪処理を行った。な
お、同図中、2は溶銑大樋、8はスキンマー、5は傾注
樋、6はトビード、(イ)は脱珪処理前の溶銑サンプリ
ング位置、(ロ)は脱珪処理後の溶銑サンプリング位置
を示T0転炉ダストのみからなる脱珪剤を使用した場合
には、第8図に示Tように、転炉ダストを多量に投入す
ると、当然ながらSiの低下幅ΔSi (脱珪処理前と
後のSi含有愈の差)が大きくなり、Siチは大きく低
下する。しかし、脱硫との関係においては、第4図に示
すように、ΔStが大きくなるにつれて(即ち、転炉ダ
ストの投入量を増加するにつれて)、脱珪処理によるS
の低下幅ΔS(脱珪処理前と後のS含有量の差)が小さ
くなり、溶銑中のSの含有量の上昇が者しくなる。
Eight types were prepared, including one in which converter dust was mixed at a ratio of eight parts to one part lime, and one in which light burnt dolomite was mixed in various ratios to converter dust, and as shown in the desiliconization flow in Fig. 2,
These desiliconizing agents 8 are transferred to the hopper 7 in a 4000 m° class blast furnace 1.
Desiliconization treatment was carried out by pouring the hot metal into the branch trough 4. In addition, in the same figure, 2 is the hot metal gutter, 8 is the skimmer, 5 is the tilting trough, 6 is the tobedo, (a) is the hot metal sampling position before the desiliconization process, and (b) is the hot metal sampling position after the desiliconization process. When using a desiliconization agent consisting only of T0 converter dust, as shown in Fig. 8, if a large amount of converter dust is introduced, the Si reduction width ΔSi (before and after desiliconization treatment) will naturally change. (difference in Si content) increases, and Si content decreases significantly. However, in relation to desulfurization, as shown in Figure 4, as ΔSt increases (that is, as the input amount of converter dust increases), the S
The decrease width ΔS (the difference between the S content before and after the desiliconization treatment) becomes smaller, and the increase in the S content in the hot metal becomes more likely.

この溶銑中のS含有量上昇は、トピード中の脱硫スラグ
が脱珪スラグと反応Tることによる現象であることは既
述のとおりであるが、この点に関し、本発明者等は転炉
ダストに軽焼ドロマイトを混合して使用したところ、軽
焼ドロマイトの混合割合3太きくするにつれて脱珪時の
Sの上昇を防止し得、かつ逆に脱硫作用も同時に発揮し
得る場合があることを見い出した。
As mentioned above, this increase in the S content in the hot metal is a phenomenon caused by the reaction between the desulfurization slag in the torpedo and the desiliconization slag. When light calcined dolomite was used in combination, it was found that as the mixing ratio of light calcined dolomite was increased by 3, the increase in S during desiliconization could be prevented, and conversely, the desulfurization effect could also be exerted at the same time. I found it.

その実験結果を第5図に示す。これより、転炉ダストに
対する軽焼ドロマイトの混合率が約30チ以上であると
、復硫防止の効果が得られ、脱硫の効果も期待できるこ
とがわかる。
The experimental results are shown in FIG. This shows that when the mixing ratio of light burnt dolomite to converter dust is about 30 or more, the effect of preventing resulfurization can be obtained and the effect of desulfurization can also be expected.

一方、転炉ダストに石灰を混合した脱珪剤2使用した場
合には、脱硫能が低下することが判明した0 即ち、転炉ダストに軽焼ドロマイ)F前述の約80%近
傍に相当する8:1の割合で混合した脱珪剤(A)と転
炉ダストに石灰を同様の割合8:1で混合した脱珪剤(
B)とについて、転炉ダストのみの脱珪剤(0)と対比
して実験したところ、第6図に示すように、石灰を混合
した場合(B)には、転炉ダストのみの場合(C)に比
較すれば、溶銑中のS含有量の上昇乃至復硫を一応防止
し得るものの、本発明の如く軽焼ドロマイトを混合した
場合(A)に比べ、脱硫能に明らかな低下がみられる。
On the other hand, when desiliconizing agent 2 containing lime was used in converter dust, it was found that the desulfurization ability decreased (i.e., the desulfurization ability of the converter dust was approximately 80%). A desiliconizing agent (A) mixed in a ratio of 8:1 and a desiliconizing agent (A) mixed with converter dust and lime in a similar ratio of 8:1
B) was compared with the desiliconizing agent (0) containing only converter dust, and as shown in Figure 6, when lime was mixed (B), the desiliconizing agent containing only converter dust ( Compared to C), although it is possible to prevent the increase in S content in the hot metal and resulfurization, there is a clear decrease in desulfurization ability compared to (A) when lightly calcined dolomite is mixed as in the present invention. It will be done.

これは、既に述べたとおり、石灰系は、サルファイドキ
ャパシティは高いものの、高粘度であるため、滓化性が
悪く、脱硫能が低化しているためである。
This is because, as already mentioned, lime-based materials have a high sulfide capacity, but have a high viscosity, resulting in poor slag formation and low desulfurization ability.

以上、詳述したところから明らかなように、本発明は転
炉ダストに軽焼ドロマイトを混合せしめて脱珪剤とTる
ものであるから、低粘度で滓化性の良好なスラグを形成
し、脱珪時の復硫を効果的に防止し得ると共に脱硫も同
時に可能としつつ、効率的に脱珪を達成できるので、そ
の作用効果は顕著である。
As is clear from the above detailed description, since the present invention mixes lightly calcined dolomite with converter dust and uses it as a desiliconizing agent, it forms a slag with low viscosity and good slagability. The effect is remarkable because it can effectively prevent resulfurization during desiliconization, and at the same time enable desulfurization and efficiently accomplish desiliconization.

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

第1図は脱珪スラグの組成と粘度の関係を表わT Oa
O−MgO−5in2の等粘度線の三角ダイヤグラム(
一部)、 第2図は脱珪フローを示す概略説明図、第3図及び第4
図は従来の脱珪剤(転炉ダスト)を使用した場合のΔS
i1 ΔSを示す図であって、第8図は脱珪剤原単位と
ΔS土の関tAE示し、第4図は第3図の場合における
ΔSiとΔSの関係を示し。 第5図は本発明に係る転炉ダストと軽焼ドロマ(8) イトの混合脱珪剤企使用した場合の混合率とΔSの関係
を示し、 第6図はΔSiとΔSの関係について従来の脱珪剤と本
発明の一実施例と2比校して示した図である0 4・・・溶銑枝樋 6・・・ドビード ア・・・ホッパー 8・・・脱珪剤。 特許出願人 川崎製鉄株式会社 第1図 MyO(wt%) 第2図 第3図 4町べ、¥y′ダχトA1竿イ立(K5/七−r)第4
図 (ンら)S’l/ (う6ン gI7
Figure 1 shows the relationship between the composition and viscosity of desiliconized slag.
Triangular diagram of isoviscosity lines for O-MgO-5in2 (
Figure 2 is a schematic explanatory diagram showing the desiliconization flow, Figures 3 and 4
The figure shows ΔS when conventional desiliconizing agent (converter dust) is used.
i1 ΔS, FIG. 8 shows the relationship tAE between the desiliconization unit and ΔS soil, and FIG. 4 shows the relationship between ΔSi and ΔS in the case of FIG. 3. Figure 5 shows the relationship between the mixing ratio and ΔS when a mixed desiliconizing agent of converter dust and light calcined doloma (8)ite according to the present invention is used, and Figure 6 shows the relationship between ΔSi and ΔS compared to the conventional method. This is a diagram showing a comparison between a desiliconizing agent and an embodiment of the present invention. 4. Hot metal branch trough 6. Dobby door hopper 8. Desiliconizing agent. Patent Applicant Kawasaki Steel Corporation Figure 1 MyO (wt%) Figure 2 Figure 3
Figure (nra) S'l/ (U6n gI7

Claims (1)

【特許請求の範囲】[Claims] L 酸化鉄系ダストと軽焼ドロマイトを混合してなるこ
とを特徴とTる溶銑処理用脱珪剤。
L A desiliconizing agent for hot metal treatment characterized by being made of a mixture of iron oxide dust and lightly calcined dolomite.
JP10917983A 1983-06-20 1983-06-20 Desiliconizing agent mixed with light burned dolomite for treating molten iron Pending JPS602611A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10917983A JPS602611A (en) 1983-06-20 1983-06-20 Desiliconizing agent mixed with light burned dolomite for treating molten iron

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10917983A JPS602611A (en) 1983-06-20 1983-06-20 Desiliconizing agent mixed with light burned dolomite for treating molten iron

Publications (1)

Publication Number Publication Date
JPS602611A true JPS602611A (en) 1985-01-08

Family

ID=14503655

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10917983A Pending JPS602611A (en) 1983-06-20 1983-06-20 Desiliconizing agent mixed with light burned dolomite for treating molten iron

Country Status (1)

Country Link
JP (1) JPS602611A (en)

Cited By (4)

* 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
JPH04325614A (en) * 1991-04-25 1992-11-16 Kawasaki Steel Corp Molten iron pre-treating agent for producing stainless steel and its manufacture
JPH08200297A (en) * 1995-01-20 1996-08-06 Mitsubishi Heavy Ind Ltd Multidirectional wave forming multidivided wave making device
KR20010100203A (en) * 2000-03-16 2001-11-14 이구택 A desiliconizer for molton pig iron

Cited By (4)

* 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
JPH04325614A (en) * 1991-04-25 1992-11-16 Kawasaki Steel Corp Molten iron pre-treating agent for producing stainless steel and its manufacture
JPH08200297A (en) * 1995-01-20 1996-08-06 Mitsubishi Heavy Ind Ltd Multidirectional wave forming multidivided wave making device
KR20010100203A (en) * 2000-03-16 2001-11-14 이구택 A desiliconizer for molton pig iron

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