JPH04263004A - Method for pretreating molten iron - Google Patents
Method for pretreating molten ironInfo
- Publication number
- JPH04263004A JPH04263004A JP4227491A JP4227491A JPH04263004A JP H04263004 A JPH04263004 A JP H04263004A JP 4227491 A JP4227491 A JP 4227491A JP 4227491 A JP4227491 A JP 4227491A JP H04263004 A JPH04263004 A JP H04263004A
- Authority
- JP
- Japan
- Prior art keywords
- slag
- agent
- molten iron
- hot metal
- dephosphorizing
- 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
Links
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title abstract description 16
- 229910052742 iron Inorganic materials 0.000 title abstract description 8
- 238000000034 method Methods 0.000 title abstract description 8
- 239000002893 slag Substances 0.000 claims abstract description 26
- 238000011282 treatment Methods 0.000 claims abstract description 17
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 16
- 239000007800 oxidant agent Substances 0.000 claims abstract description 8
- 238000007654 immersion Methods 0.000 claims abstract description 7
- 239000012159 carrier gas Substances 0.000 claims abstract description 6
- 239000002184 metal Substances 0.000 claims description 32
- 229910052751 metal Inorganic materials 0.000 claims description 32
- 238000002203 pretreatment Methods 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 238000007664 blowing Methods 0.000 abstract description 9
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 abstract description 6
- 239000010436 fluorite Substances 0.000 abstract description 6
- 239000004902 Softening Agent Substances 0.000 abstract description 4
- 238000005187 foaming Methods 0.000 abstract description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 abstract 2
- 235000011941 Tilia x europaea Nutrition 0.000 abstract 2
- 239000004571 lime Substances 0.000 abstract 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 12
- 239000000292 calcium oxide Substances 0.000 description 6
- 235000012255 calcium oxide Nutrition 0.000 description 6
- 230000004907 flux Effects 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- 230000005587 bubbling Effects 0.000 description 1
- 238000006477 desulfuration reaction Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】この発明は、溶銑の予備処理方法
に関し、とくに該予備処理時における鉄分ロスを少なく
するとともに、処理時間の効率化を図ろうとするもので
ある。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for pre-treating hot metal, and in particular aims to reduce iron loss during the pre-treatment and to improve the efficiency of the treatment time.
【0002】0002
【従来の技術】底吹きならびに上底吹きの複合吹練法が
実施されるに至った近年では、溶銑予備処理段階での脱
珪、脱りん、脱硫の各処理が不可欠とされ、各種プロセ
スが開発、実施されるようになってきた。溶銑予備処理
法の一つとして、特開昭58−16006号公報には、
ミルスケールなどの酸化剤、生石灰などの造滓剤および
蛍石などの軟化剤からなるフラックスを、N2 あるい
は圧縮空気などの運搬ガスとともに溶銑浴面下に吹き込
み、溶銑中のPと酸化剤との反応によってP2O5を生
成させ、これを溶銑浴面上に浮上させたのちは造滓剤に
よって固定して効率的な脱りんを行う手法が提案されて
いる。[Prior Art] In recent years, the combined blowing method of bottom blowing and top and bottom blowing has been implemented, and the treatments of desiliconization, dephosphorization, and desulfurization in the pretreatment stage of hot metal are essential, and various processes are It has been developed and implemented. As one of the hot metal pretreatment methods, JP-A-58-16006 discloses
A flux consisting of an oxidizing agent such as mill scale, a slag forming agent such as quicklime, and a softening agent such as fluorite is blown below the surface of the hot metal bath together with a carrier gas such as N2 or compressed air, and the oxidizing agent and P in the hot metal are mixed. A method has been proposed in which P2O5 is generated through a reaction, floated onto the surface of the hot metal bath, and then fixed with a slag-forming agent for efficient dephosphorization.
【0003】0003
【発明が解決しようとする課題】ところで、かかる手法
では、溶銑の予備処理の際に、泡立ちによりスラグが容
器からオーバーフローするようなうれいがある場合にフ
ラックスの吹き込み速度を低下させたり、フラックス中
の塩基度調整剤や酸化剤の配合割合を調整するなどして
処理時間を長くとる処置を施す必要があった。とくに処
理時間を延長する場合には温度低下によってスラグの硬
化をきたし、反応界面積が減少するためP2O5が浮上
してもスラグに固定されずに解離し、有効な脱りん処理
ができない不具合があった。なお、この点に関してはフ
ラックス中に軟化剤を含有させて対処する試みもあるけ
れども、処理時間の経過によるスラグの温度降下に対応
してフラックス中の軟化剤の配合割合を高くする必要が
あり、効率的な脱りん処理ができるとはいえないのが現
状であった。[Problems to be Solved by the Invention] However, in this method, during the preliminary treatment of hot metal, if there is a problem where the slag overflows from the container due to bubbling, it is necessary to reduce the flux blowing speed or It was necessary to take measures to lengthen the processing time, such as by adjusting the mixing ratio of the basicity regulator and oxidizing agent. In particular, when the treatment time is extended, the slag hardens due to temperature drop and the reaction interface area decreases, so even if P2O5 floats to the surface, it dissociates without being fixed to the slag, and there is a problem that effective dephosphorization cannot be performed. Ta. Although some attempts have been made to address this issue by incorporating a softener into the flux, it is necessary to increase the blending ratio of the softener in the flux in response to the drop in temperature of the slag over the course of processing time. At present, it cannot be said that efficient dephosphorization treatment is possible.
【0004】上述したような従来の問題を解決し効率的
な処理ができる溶銑予備処理方法を提案することがこの
発明の目的である。It is an object of the present invention to propose a hot metal pretreatment method that solves the above-mentioned conventional problems and enables efficient treatment.
【0005】[0005]
【課題を解決するための手段】この発明は、溶銑の脱り
ん処理に当たり、一端を溶銑の浴中に浸漬した浸漬ラン
スより酸化剤と造滓剤からなる脱りん剤を運搬ガスとと
もに吹き込む一方、溶銑の浴面上に塩基度調整剤及び軟
化剤を添加することによってスラグの滓化を制御するこ
とを特徴とする溶銑予備処理方法である。[Means for Solving the Problems] In the dephosphorization treatment of hot metal, the present invention involves blowing a dephosphorizing agent consisting of an oxidizing agent and a slag-forming agent together with a carrier gas through an immersion lance whose one end is immersed in a bath of hot metal; This hot metal pretreatment method is characterized in that slag formation is controlled by adding a basicity regulator and a softener onto the hot metal bath surface.
【0006】[0006]
【作用】脱りん処理時にミルスケールなどの酸化剤、生
石灰などの造滓剤および蛍石などの軟化剤からなるフラ
ックスを、N2 あるいは圧縮空気などの運搬ガスとと
もに溶銑浴面下に吹き込む方式のものでは、処理状況や
フラックスの配合割合の関係上処理時間を延長せざるを
得ない場合があるのは前述した通りである。ここに、脱
りん処理時におけるスラグのオーバーフローは、脱りん
処理の初期(脱珪期)に多くみられ、とくにスラグ中の
SiO2の濃度が高く、塩基度(CaO/SiO2)が
1.5 以下と低い場合に発生する。このためこの発明
では、この時期に生石灰等の塩基度調整剤を溶銑欲面上
に添加してスラグの塩基度を高くするようにしてスラグ
の泡立ちを抑制し、容器からのオーバーフローを防止す
る。また、処理時間の経過とともにスラグの温度は降下
し、前述したようにスラグの硬化によって処理能率が低
下するので、蛍石などのスラグ軟化剤についても溶銑浴
面上に添加することとした。この発明において、塩基度
調整剤およびスラグ軟化剤を溶銑浴面上に添加するのは
、溶銑の浴中に吹き込む酸化剤の添加比率を変更する必
要がなく、処理時間の短縮化に有利だからである。とく
に、スラグのオーバーフローを抑制する場合には、塩基
度調整剤の吹き込み速度を低下させる必要がなく処理時
間の短縮化を図ることができる。[Operation] During dephosphorization, a flux consisting of an oxidizing agent such as mill scale, a slag forming agent such as quicklime, and a softening agent such as fluorite is blown into the surface of the hot metal bath together with a carrier gas such as N2 or compressed air. As mentioned above, the processing time may have to be extended due to the processing conditions and flux blending ratio. Here, slag overflow during dephosphorization is often seen in the initial stage of dephosphorization (desilication stage), especially when the concentration of SiO2 in the slag is high and the basicity (CaO/SiO2) is 1.5 or less. Occurs when the temperature is low. For this reason, in this invention, a basicity regulator such as quicklime is added to the hot metal surface at this time to increase the basicity of the slag, thereby suppressing foaming of the slag and preventing overflow from the container. Furthermore, the temperature of the slag decreases with the passage of processing time, and as mentioned above, the processing efficiency decreases due to hardening of the slag, so it was decided to add a slag softener such as fluorite to the surface of the hot metal bath. In this invention, the basicity regulator and slag softener are added onto the surface of the hot metal bath because it is not necessary to change the addition ratio of the oxidizing agent blown into the hot metal bath and is advantageous in shortening the processing time. be. In particular, when suppressing slag overflow, there is no need to reduce the blowing speed of the basicity regulator, and the processing time can be shortened.
【0007】図1は、この発明を実施するのに用いて好
適な装置の一例を示したものであり、図中1は溶銑を収
容するトピードカー、2は溶銑、3はスラグ、4は一端
を溶銑浴中に浸漬した浸漬ランスであって、このランス
4は脱りん用の造滓剤を例えばN2 のような搬送ガス
とともに溶銑浴中に吹き込む。5、6は塩基度調整剤や
軟化剤を収容する容器、7は容器5、6内の収容物を払
い出すための装置、そして8は温度補償のために使用す
る酸素吹き込みランスである。FIG. 1 shows an example of an apparatus suitable for carrying out the present invention. In the figure, 1 is a torpedo car containing hot metal, 2 is a torpedo car containing hot metal, 3 is a slag, and 4 is a torpedo car containing one end. An immersion lance 4 is immersed in a hot metal bath, and this lance 4 blows a slag forming agent for dephosphorization into the hot metal bath together with a carrier gas such as N2. Reference numerals 5 and 6 designate containers containing basicity regulators and softeners, 7 a device for discharging the contents in the containers 5 and 6, and 8 an oxygen blowing lance used for temperature compensation.
【0008】[0008]
【実施例】上掲図1に示したようなトピードカーに、2
80 t の高炉溶銑を収容し、溶銑1t当たり15k
gのミルスケールを添加してSi含有量が0.10%と
なるまで脱Si処理を施し、次いで脱Si処理で生成し
たスラグを約1.0 kg/t−p になるまで取り除
いてから、浸漬ランスを用いてミルスケール、生石灰お
よび蛍石からなる脱りん剤、造滓剤をそれぞれ溶銑1t
当たり30kg、10kg、2kgをN2 ガスととも
に溶銑浴中に吹き込んで脱りん処理を施し、溶銑ロス、
脱りん処理にかかる時間等について調査した。
なお溶銑浴面上からは、脱りん処理の初期に生石灰を5
kg/t−p 、また脱りん処理の中期に蛍石を2kg
/t−p 添加した。その結果を、従来法にしたがって
脱りん処理を施した場合の結果と比較して表−1に示す
。[Example] In a torpedo car as shown in Figure 1 above, 2
It accommodates 80 tons of blast furnace hot metal and produces 15k per ton of hot metal.
g of mill scale was added to perform Si removal treatment until the Si content became 0.10%, and then the slag produced in the Si removal treatment was removed until it became about 1.0 kg/t-p. Using an immersion lance, add 1 ton of mill scale, a dephosphorizing agent and a slag-forming agent consisting of quicklime and fluorite to hot metal.
30kg, 10kg, and 2kg of each are blown into the hot metal bath together with N2 gas to perform dephosphorization treatment, reduce hot metal loss,
We investigated the time required for dephosphorization treatment. In addition, from above the surface of the hot metal bath, 5 liters of quicklime was added at the beginning of the dephosphorization process.
kg/t-p, and 2 kg of fluorite in the middle stage of dephosphorization treatment.
/t-p added. The results are shown in Table 1 in comparison with the results when dephosphorization was performed according to the conventional method.
【0009】[0009]
【表1】[Table 1]
【0010】脱P造滓剤、塩基度調整剤および軟化剤を
すべて溶銑浴中に吹き込む従来法を適用した場合に比較
し、この発明に従う適合例では処理時間の短縮が可能で
あり、スラグのオーバーフローによる溶銑ロスが極めて
小さいことが確かめられた。[0010] Compared to the conventional method in which a dephosphorizing slag agent, basicity regulator, and softener are all blown into the hot metal bath, the adapted example according to the present invention can shorten the processing time and reduce the amount of slag. It was confirmed that the loss of hot metal due to overflow was extremely small.
【0011】[0011]
【発明の効果】かくしてこの発明によれば、(1)脱り
ん処理時におけるスラグの泡立ちによるオーバーフロー
を抑制できるので鉄分ロスが小さく、操業上のトラブル
も極めて少ない。
(2)処理時間の短縮によって、生産性を著しく向上さ
せることができる。
(3)効率の高い脱りん処理ができるので、下工程での
脱りん負荷を減少させることができる。Thus, according to the present invention, (1) overflow due to foaming of slag during dephosphorization treatment can be suppressed, so iron loss is small and operational troubles are extremely small. (2) Productivity can be significantly improved by shortening processing time. (3) Since highly efficient dephosphorization treatment can be performed, the dephosphorization load in downstream processes can be reduced.
【図1】図1はこの発明の実施に使用して好適な設備の
構成説明図である。FIG. 1 is an explanatory diagram of the configuration of equipment suitable for use in implementing the present invention.
1 トピードカー 2 溶接 3 スラグ 4 浸漬ランス 5 容器 6 容器 7 払い出し装置 8 酸素吹き込みランス 1 Torpedo car 2 Welding 3. Slag 4 Immersion lance 5 Container 6 Container 7 Dispensing device 8 Oxygen blowing lance
Claims (1)
銑の浴中に浸漬した浸漬ランスより酸化剤と造滓剤から
なる脱りん剤を運搬ガスとともに吹き込む一方、溶銑の
浴面上に塩基度調整剤及び軟化剤を添加することによっ
てスラグの滓化を制御することを特徴とする溶銑予備処
理方法。Claim 1: During the dephosphorization treatment of hot metal, a dephosphorizing agent consisting of an oxidizing agent and a slag-forming agent is blown in together with a carrier gas through an immersion lance whose one end is immersed in the hot metal bath, while a basicity A hot metal pretreatment method characterized by controlling slag formation by adding a conditioner and a softener.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP04227491A JP3330960B2 (en) | 1991-02-15 | 1991-02-15 | Hot metal pretreatment method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP04227491A JP3330960B2 (en) | 1991-02-15 | 1991-02-15 | Hot metal pretreatment method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04263004A true JPH04263004A (en) | 1992-09-18 |
JP3330960B2 JP3330960B2 (en) | 2002-10-07 |
Family
ID=12631459
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP04227491A Expired - Lifetime JP3330960B2 (en) | 1991-02-15 | 1991-02-15 | Hot metal pretreatment method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3330960B2 (en) |
-
1991
- 1991-02-15 JP JP04227491A patent/JP3330960B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP3330960B2 (en) | 2002-10-07 |
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