JPH08199219A - Dephosphorizing method of molten iron - Google Patents

Dephosphorizing method of molten iron

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Publication number
JPH08199219A
JPH08199219A JP7008506A JP850695A JPH08199219A JP H08199219 A JPH08199219 A JP H08199219A JP 7008506 A JP7008506 A JP 7008506A JP 850695 A JP850695 A JP 850695A JP H08199219 A JPH08199219 A JP H08199219A
Authority
JP
Japan
Prior art keywords
slag
concentration
treatment
rate
blown
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
JP7008506A
Other languages
Japanese (ja)
Other versions
JP3345677B2 (en
Inventor
Yuji Ogawa
雄司 小川
Shinya Kitamura
信也 北村
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
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Nippon Steel Corp
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Priority to JP00850695A priority Critical patent/JP3345677B2/en
Publication of JPH08199219A publication Critical patent/JPH08199219A/en
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Publication of JP3345677B2 publication Critical patent/JP3345677B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
  • Carbon Steel Or Casting Steel Manufacturing (AREA)

Abstract

PURPOSE: To provide the dephosphorizing method in which P hit rate after treatment is improved, flux consumption unit is reduced and lowering of yield of iron is extremely suppressed. CONSTITUTION: In the dephosphorizing method of molten iron in which the bottom agitating power is >=1.0kw/t, the top blowing oxygen supply rate is >=2.5Nm<3> /min/t, CaO/SiO2 in the slag after treatment is >=0.6 to <=2.5, the treatment completing temp. is 1250-1400 deg.C, the top blowing oxygen supply rate, bottom blowing gas flow rate and a height of the top blowing lance are controlled so as to turn the T. Fe concentration in slag, which is calculated by the equation, T. Fe concentration (weight %) in slag = 6.49×(top blowing oxygen supply rate) (Nm<3> /min/t)-15.35×(L/L0 )+9.68|2-CaO/SiO2 |+11.73, (wherein, L: recessed depth of molten steel due to top blowing, L0 : standstill molten steel depth) to 10-20.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は転炉内での溶銑の脱りん
方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for dephosphorizing hot metal in a converter.

【0002】[0002]

【従来の技術】製鋼トータルコストのミニマム化や低り
ん鋼の安定溶銑に関して、従来溶銑の脱りん法として、
(1)トーピードカー内の溶銑に脱りん用フラックスを
インジェクションして予備脱りんを行う方法、(2)取
鍋内の溶銑に脱りん用フラックスをインジェクションす
るか、もしくは吹き付けを行い、予備脱りんを行う方
法、あるいは(3)2基の転炉を用いて、一方で脱りん
を行い、他方で脱炭を行う方法(例えば、特開昭63−
195210号公報)が用いられている。
2. Description of the Related Art Regarding the minimization of the total cost of steelmaking and the stable hot metal of low phosphorus steel, the conventional hot metal dephosphorization method is as follows.
(1) Method for pre-dephosphorization by injecting flux for dephosphorization into hot metal in torpedo car, (2) Pre-dephosphorization by injecting or spraying flux for dephosphorization on hot metal in ladle Or (3) using two converters for dephosphorization on the one hand and decarburization on the other hand (see, for example, JP-A-63-
195210) is used.

【0003】しかしながら、トーピードカーを用いた場
合、攪拌が弱いため脱りん反応は平衡から遠く、目標の
脱りん量を達成するために必要以上の生石炭等のフラッ
クスを使用しなければならずフラックス原単位が高いと
いう問題がある。また、トーピードカーや溶銑鍋を処理
容器として用いる場合、上吹き送酸速度を大きくして処
理時間を短縮しようとすると、フリーボードが小さいた
めにスラグの泡立ちによる操業上の障害が生じる。プロ
セス(1)で約20分、プロセス(2)で約11分が脱
りん工程の最短処理時間であるのが現状であった。ま
た、プロセス(3)においても送酸速度は高々1.0N
3 /min/tで操業されており、処理時間も約10
分を要していた。
However, when a torpedo car is used, the dephosphorization reaction is far from equilibrium because the stirring is weak, and more flux than necessary is used to achieve the target dephosphorization amount, such as raw coal. There is a problem that the unit is high. Further, when a torpedo car or a hot metal ladle is used as a processing container, if the top blowing acid speed is increased and the processing time is shortened, the freeboard is small, which causes a problem in operation due to foaming of slag. Under the present circumstances, the shortest treatment time of the dephosphorization step is about 20 minutes in the process (1) and about 11 minutes in the process (2). Also, in the process (3), the acid transfer rate is 1.0 N at most.
It is operated at m 3 / min / t and the processing time is about 10
It took a minute.

【0004】本発明者らは、かかる問題点を解決するた
め、種々の脱りん実験を行い、下記のことを明らかにし
た。 底吹き攪拌動力を1kW/t以上に確保することによ
り、ほぼ平衡まで脱りん反応が進行すること。 その結果、処理後温度1250〜1400℃の範囲で
は、温度に応じて処理後のスラグ中CaO/SiO2
0.6〜2.5で十分に目標の脱りん量に達すること。
The present inventors have conducted various dephosphorization experiments in order to solve such problems, and have clarified the following. By ensuring the bottom blowing stirring power of 1 kW / t or more, the dephosphorization reaction progresses to almost equilibrium. As a result, in the range of the post-treatment temperature of 1250 to 1400 ° C, CaO / SiO 2 in the slag after the treatment is 0.6 to 2.5 and the target dephosphorization amount is sufficiently reached depending on the temperature.

【0005】送酸速度が2.5Nm3 /min/t以
上の高送酸速度下では、脱りん酸素効率の低下がさほど
認められず、脱りん速度定数が向上し、脱りん処理時間
の短縮が可能であること。 処理後のスラグ中T.Fe濃度を10〜20重量%に
することで、脱りん反応をより適正化でき、鉄歩留りを
維持しつつフラックス原単位を低減できること。
At a high acid transfer rate of 2.5 Nm 3 / min / t or more, the dephosphorization oxygen efficiency is not significantly reduced, the dephosphorization rate constant is improved, and the dephosphorization treatment time is shortened. Is possible. T. in slag after treatment By adjusting the Fe concentration to 10 to 20% by weight, the dephosphorization reaction can be made more appropriate, and the flux basic unit can be reduced while maintaining the iron yield.

【0006】これらの事実に基づき、「フラックス添加
と酸素上吹きおよび底吹き攪拌とを行って溶銑を脱りん
精錬する際に、底吹き攪拌動力が1.0kW/t以上、
上吹き送酸速度が2.5Nm3 /min/t以上、処理
終点温度が1250℃以上1400℃以下、処理後のス
ラグ中CaO/SiO2 が0.6以上2.5以下、T.
Fe濃度が10〜20重量%であることを特徴とする溶
銑の脱りん方法」(特願平05−165790号)を先
に提案し、これにより(1)見かけ平衡に近いところま
で脱りん反応が進行するような十分大きな底吹き攪拌を
与えて、処理温度に応じた最低必要量まで生石灰等のフ
ラックス原単位を低減すること、および(2)送酸速度
を高めることにより処理時間を短縮することを可能にし
た。
Based on these facts, "When the flux addition and oxygen top blowing and bottom blowing stirring are performed to dephosphorize the hot metal, the bottom blowing stirring power is 1.0 kW / t or more,
Top blowing acid rate is 2.5 Nm 3 / min / t or more, treatment end point temperature is 1250 ° C. or more and 1400 ° C. or less, CaO / SiO 2 in the slag after treatment is 0.6 or more and 2.5 or less, T.I.
A method for dephosphorizing hot metal, characterized in that the Fe concentration is 10 to 20% by weight (Japanese Patent Application No. 05-165790), was proposed. The amount of flux basic unit such as quick lime is reduced to the minimum required amount according to the treatment temperature by giving a sufficiently large bottom-blown agitation so that the process proceeds, and (2) shortening the treatment time by increasing the acid transfer rate. Made it possible.

【0007】しかしながら、上述の脱りん方法におい
て、底吹き攪拌動力は溶銑量・溶銑温度・底吹きガス流
量から、上吹き送酸速度は溶銑量から予め計算でき、処
理終点温度は熱バランス計算により、処理後のスラグ中
CaO/SiO2 はフラックス量と溶銑成分から配合計
算により推定できるものの、スラグ中T.Fe濃度に関
しては、底吹き攪拌動力、上吹き送酸速度・ランス高
さ、スラグ組成との関係式がこれまでなく、処理前に推
定することが困難で、処理後のスラグを分析するまで判
らないのが実状であった。そのため、送酸速度を変更す
る際や、スクラップ使用量や転炉での脱炭吹止め温度等
の変化に対して熱バランスから溶銑脱りん処理終点の温
度を変更し、それに応じてスラグ中CaO/SiO2
変更する際、処理後のスラグ中T.Feが目標とする1
0〜20重量%から外れ、(1)目標の[P]レベルに
到達しない、(2)[P]外れを防止するためフラック
スを余分に投入しフラックス原単位の平均値が増加す
る、(3)鉄歩留りが悪化するといった障害がしばしば
生じていた。
However, in the above-mentioned dephosphorization method, the bottom blowing stirring power can be calculated in advance from the amount of hot metal, the temperature of hot metal, and the flow rate of bottom blowing gas, and the rate of top blowing acid can be calculated in advance from the amount of hot metal. , CaO / SiO 2 in the slag after the treatment can be estimated from the flux amount and the hot metal component by a blending calculation, but the T.O. Regarding the Fe concentration, there is no relational expression among bottom-blown stirring power, top-blown acid feed rate / lance height, and slag composition, which is difficult to estimate before treatment, and it is known until the slag after treatment is analyzed. The reality was that there was nothing. Therefore, when changing the acid transfer rate, or when changing the amount of scrap used or the decarburization stop temperature in the converter, the temperature of the hot metal dephosphorization end point is changed from the heat balance, and CaO in the slag is changed accordingly. When changing SiO 2 / SiO 2 , the T. Fe is the target 1
It deviates from 0 to 20% by weight, (1) the target [P] level is not reached, (2) extra flux is added to prevent the [P] deviation, and the average value of the flux basic unit increases (3 ) There were often obstacles such as deterioration of iron yield.

【0008】[0008]

【発明が解決しようとする課題】本発明は、前述の問題
点を解決すべく、脱りん処理後のスラグ中T.Fe濃度
を事前に予測し、該濃度が10〜20重量%となるよう
に上吹き送酸速度、ランス高さ、底吹き攪拌動力を調整
して、脱りん反応が適正化された状態で処理を行い、処
理後の[P]濃度を精度良く制御するとともに、平均の
フラックス原単位を低減し、かつ鉄歩留りの低下を極力
抑えようとするものである。
SUMMARY OF THE INVENTION In order to solve the above-mentioned problems, the present invention provides a T.S. Predict the Fe concentration in advance, adjust the top-blowing acid feeding rate, lance height, and bottom-blown stirring power so that the concentration will be 10 to 20% by weight, and treat in a state where the dephosphorization reaction is optimized. Is carried out to accurately control the [P] concentration after the treatment, reduce the average flux basic unit, and suppress the reduction of the iron yield as much as possible.

【0009】すなわち、本発明は、処理後の[P]的中
率を向上し、フラックス原単位を低減し、かつ鉄歩留り
の低下を極力抑えた溶銑の脱りん法を提供するものであ
る。
That is, the present invention provides a hot metal dephosphorization method in which the [P] hit ratio after treatment is improved, the flux basic unit is reduced, and the decrease in iron yield is suppressed as much as possible.

【0010】[0010]

【課題を解決するための手段】本発明の要旨とするとこ
ろは下記の通りである。フラックス添加と酸素上吹きお
よび底吹き攪拌とを行って溶銑を脱りん精錬する際に、
底吹き攪拌動力が1.0kW/t以上、上吹き送酸速度
が2.5Nm3/min/t以上、処理後のスラグ中C
aO/SiO2 が0.6以上2.5以下、処理終点温度
が1250℃以上1400℃以下であることを特徴とす
る溶銑の脱りん方法において、式(1)で計算されるス
ラグ中T.Fe濃度が10〜20重量%となるように、
上吹き送酸速度、底吹きガス流量、上吹きランス高さを
制御することを特徴とする溶銑の脱りん方法。
The gist of the present invention is as follows. When dephosphorizing and refining the hot metal by performing flux addition and oxygen top blowing and bottom blowing stirring,
Bottom blowing stirring power is 1.0 kW / t or more, top blowing acid feeding rate is 2.5 Nm 3 / min / t or more, C in slag after treatment
aO / SiO 2 is 0.6 or more and 2.5 or less, and the treatment end point temperature is 1250 ° C. or more and 1400 ° C. or less. So that the Fe concentration is 10 to 20% by weight,
A method for dephosphorizing hot metal, which comprises controlling the rate of top blowing acid, the flow rate of bottom blowing gas, and the height of top blowing lance.

【0011】 スラグ中T.Fe濃度(重量%) =6.49×(上吹き送酸速度)(Nm3/min/t)−5.73×(底吹き攪拌動力)(kW/t) −15.35 ×(L/LO )+9.68|2−CaO/SiO2|+11.73 (1) 以下本発明を詳述する。本発明は、まず底吹き機能の付
いた転炉内に溶銑を装入した後、フラックスを上方もし
くは底吹きインジェクションにより添加し、上吹きラン
スから酸素ガスを吹き付け、底からガス攪拌を行いつ
つ、脱りん精錬を行う。この際、特願平05−1657
90号で示したように、底吹き攪拌動力が1.0kW/
t以上、上吹き送酸速度が2.5Nm3 /min/t以
上、処理終点温度が1250℃以上1400℃以下、処
理後のスラグ中CaO/SiO2 が0.6以上2.5以
下、T.Fe濃度が10〜20重量%とすることで、フ
ラックス原単位を低減し、かつ鉄歩留り低下を極力抑え
た、短時間での脱りん処理が可能となる。
Slag T. Fe concentration (wt%) = 6.49 × (the top-blown oxygen-flow-rate) (Nm 3 / min / t ) -5.73 × ( bottom blowing agitation power) (kW / t) -15.35 × (L / L O) +9.68 | 2-CaO / SiO 2 | +11.73 (1) The present invention is described in detail below. The present invention, first, after charging the hot metal into the converter with a bottom blowing function, the flux is added by upward or bottom blowing injection, blowing oxygen gas from the top blowing lance, while performing gas stirring from the bottom, Perform dephosphorization refining. At this time, Japanese Patent Application No. 05-1657
As shown in No. 90, the bottom blowing stirring power is 1.0 kW /
t or more, the rate of acid to be blown up is 2.5 Nm 3 / min / t or more, the treatment end point temperature is 1250 ° C. or more and 1400 ° C. or less, CaO / SiO 2 in the slag after treatment is 0.6 or more and 2.5 or less, T . By setting the Fe concentration to 10 to 20% by weight, it becomes possible to perform the dephosphorization treatment in a short time while reducing the flux basic unit and suppressing the iron yield reduction as much as possible.

【0012】本発明者らは種々の脱りん実験を行い、処
理後のスラグ中T.Fe濃度と、上吹き送酸速度、ラン
ス高さ、底吹き攪拌動力、スラグ中CaO/SiO2
の関係を調査し、重回帰分析から(1)式で示す関係を
見出した。 スラグ中T.Fe濃度(重量%) =6.49×(上吹き送酸速度)(Nm3/min/t)−5.73×(底吹き攪拌動力)(KW/t) −15.35 ×(L/LO )+9.68|2−CaO/SiO2|+11.73 (1) L :上吹きジェットによる溶鋼の凹み深さ (mm) LO :静止溶鋼深さ (mm) ここで、底吹き攪拌動力は(2)式から(第101,1
02回西山記念技術講座、日本鉄鋼協会、1984,
p.73)計算される値を使用する。
The present inventors have conducted various dephosphorization experiments and carried out T. The relationship between the Fe concentration, the top-blown acid flow rate, the lance height, the bottom-blown stirring power, and CaO / SiO 2 in the slag was investigated, and the relationship shown by the equation (1) was found from multiple regression analysis. T. in slag Fe concentration (wt%) = 6.49 × (the top-blown oxygen-flow-rate) (Nm 3 / min / t ) -5.73 × ( bottom blowing agitation power) (KW / t) -15.35 × (L / L O) +9.68 │2-CaO / SiO 2 │ + 11.73 (1) L: Depth of molten steel by top-blown jet (mm) L O : Stationary molten steel depth (mm) Where, bottom-blown stirring power is formula (2) From (No. 101, 1
02nd Nishiyama Memorial Technical Lecture, Iron and Steel Institute of Japan, 1984,
p. 73) Use the calculated value.

【0013】[0013]

【数1】 [Equation 1]

【0014】また、Lは(3)式から(「鉄冶金反応工
学」,日刊工業新聞社,1969,p.94)計算され
る値を使用する。 L=Lh ・exp(−0.78h/Lh ) (3) Lh =63.0(kFO2/nd)2/3 h :静止湯面からのランス高さ(mm) k :ジェットの干渉係数(−) FO2:上吹き酸素流量(Nm3 /h) n :ランスの孔数(−) d :ランスの孔径(mm) 種々の脱りん実験における処理後のスラク中T.Fe濃
度と(1)式から計算されるT.Fe濃度との関係を図
1に示す。(1)式により処理後のスラグ中T.Fe濃
度を非常に精度良く推定でき、特願平05−16579
0号で示したような、フラックス原単位を低減し、鉄歩
留り低下を極力抑えた効率の良い脱りん処理条件を安定
して実現できることが明らかになった。
Further, L is a value calculated from the equation (3) (“Iron Metallurgical Reaction Engineering”, Nikkan Kogyo Shimbun, 1969, p.94). L = L h · exp (−0.78 h / L h ) (3) L h = 63.0 (kF O2 / nd) 2/3 h: Lance height (mm) from stationary surface k: Jet Interference coefficient (−) F O2 : Top-blown oxygen flow rate (Nm 3 / h) n: Number of holes in lance (−) d: Hole diameter of lance (mm) T.S. in slack after treatment in various dephosphorization experiments. The T.F. calculated from the Fe concentration and the equation (1). The relationship with the Fe concentration is shown in FIG. According to the equation (1), the T. Fe concentration can be estimated very accurately, and Japanese Patent Application No. 05-16579
It has been clarified that it is possible to stably realize the efficient dephosphorization treatment condition in which the flux basic unit is reduced and the iron yield reduction is suppressed as much as shown in No. 0.

【0015】[0015]

【実施例】8t試験転炉を用いて、脱りん実験を10チ
ャージ実施した。4.3〜4.6%のC,約0.1%の
P,約0.3%のSiを含む初期温度1180〜130
0℃の約6tの溶銑を6分間精錬した。フラックスとし
て生石灰を処理後のCaO/SiO2 が1.5となるよ
うに配合計算して投入した。上吹き送酸速度は2.5〜
3.5Nm3 /min/t、底吹きはN2 ガス200,
300Nm3 /h(2.0,3.0kW/t)の2条件
で精錬を行い、その際、(1)式から計算されるT.F
e濃度が15%になるようにL/L0 を決定し、(3)
式からランス高さを求めた。また、処理後の溶銑温度が
1350℃一定となるように、スクラップ量を適宜被処
理溶銑と配合した。
EXAMPLE A dephosphorization experiment was carried out for 10 charges using an 8t test converter. Initial temperature 1180-130 containing 4.3-4.6% C, about 0.1% P, about 0.3% Si
About 6 tons of hot metal at 0 ° C. was refined for 6 minutes. Quick lime was used as a flux after calculating the blending ratio so that the CaO / SiO 2 after treatment was 1.5. Top blowing acid rate is 2.5-
3.5 Nm 3 / min / t, bottom blowing is N 2 gas 200,
Refining was carried out under two conditions of 300 Nm 3 / h (2.0, 3.0 kW / t), and at that time, the T.S. calculated from the formula (1) was used. F
L / L 0 is determined so that the e concentration becomes 15%, and (3)
The lance height was calculated from the formula. Further, the amount of scrap was appropriately mixed with the hot metal to be treated so that the hot metal temperature after the treatment was constant at 1350 ° C.

【0016】表1、表2(表1のつづき)に、本実施例
における諸元と(1)式から計算されるスラグ中T.F
e濃度と実績T.Fe濃度、目的の[P]濃度と実績
[P]濃度、鉄歩留りおよび生石灰原単位を示す。スラ
グ中T.Fe濃度は計算値の±2%に制御されているこ
とが判る。また、全てのチャージで[P]濃度は目標
[P]濃度以下となっており、制御性が良く効率的な脱
りん処理であることを示している。
Tables 1 and 2 (continued from Table 1) show T.S. in slag calculated from the specifications in this embodiment and the equation (1). F
e Concentration and actual results Fe concentration, target [P] concentration and actual [P] concentration, iron yield, and quick lime basic unit are shown. T. in slag It can be seen that the Fe concentration is controlled to ± 2% of the calculated value. Further, the [P] concentration is less than or equal to the target [P] concentration in all the charges, which shows that the dephosphorization process is efficient with good controllability.

【0017】表3には、本実施例における[P]濃度の
的中率、すなわち目標の[P]濃度に達成した割合、
[P]のバラツキ、すなわち目標[P]濃度からの偏差
の平均値、および生石灰原単位と鉄歩留りの平均値を示
す。比較として、(1)式を用いていなかった時の従来
法50チャージにおける各値を併せて示す。従来法と比
較して、[P]濃度の的中率が飛躍的に向上し、[P]
のバラツキも低下して、生石灰原単位が低減され、鉄歩
留り低下の抑制が可能であることが明らかになった。
Table 3 shows the hit rate of the [P] concentration in this embodiment, that is, the ratio of achieving the target [P] concentration,
The variation of [P], that is, the average value of the deviation from the target [P] concentration, and the average value of quick lime basic unit and iron yield are shown. For comparison, each value in the conventional method 50 charge when the formula (1) is not used is also shown. Compared with the conventional method, the accuracy rate of [P] concentration is dramatically improved,
It was clarified that the variation in the amount of iron was reduced, the basic unit of quick lime was reduced, and the reduction of iron yield could be suppressed.

【0018】[0018]

【表1】 [Table 1]

【0019】[0019]

【表2】 [Table 2]

【0020】[0020]

【表3】 [Table 3]

【0021】[0021]

【発明の効果】本発明により、処理後の[P]的中率を
向上し、フラックス原単位を低減するとともに、鉄歩留
りの向上を図ることが可能となった。
According to the present invention, it is possible to improve the [P] hit rate after the treatment, reduce the flux basic unit, and improve the iron yield.

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

【図1】(1)式で計算されるスラグ中T.Fe濃度と
実績の処理後T.Feの関係を示す図である。
FIG. 1 is a diagram showing T.S. in slag calculated by the equation (1). After the Fe concentration and the actual processing T. It is a figure which shows the relationship of Fe.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 フラックス添加と酸素上吹きおよび底吹
き攪拌とを行って溶銑を脱りん精錬する際に、底吹き攪
拌動力が1.0kW/t以上、上吹き送酸速度が2.5
Nm3 /min/t以上、処理後のスラグ中CaO/S
iO2 が0.6以上2.5以下、処理終点温度が125
0℃以上1400℃以下であることを特徴とする溶銑の
脱りん方法において、式(1)で計算されるスラグ中
T.Fe濃度が10〜20重量%となるように、上吹き
送酸速度、底吹きガス流量、上吹きランス高さを制御す
ることを特徴とする溶銑の脱りん方法。 スラグ中T.Fe濃度(重量%) =6.49×(上吹き送酸速度)(Nm3/min/t)−5.73×(底吹き攪拌動力)(kW/t) −15.35 ×(L/LO )+9.68|2−CaO/SiO2|+11.73 (1) L :上吹きジェットによる溶鋼の凹み深さ LO :静止溶鋼深さ
1. When dephosphorizing and refining the hot metal by adding flux and performing oxygen top blowing and bottom blowing stirring, the bottom blowing stirring power is 1.0 kW / t or more, and the top blowing acid feeding rate is 2.5.
Nm 3 / min / t or more, CaO / S in slag after treatment
iO 2 is 0.6 or more and 2.5 or less, and the treatment end point temperature is 125.
In the method for dephosphorizing hot metal, which is characterized in that the temperature is 0 ° C. or higher and 1400 ° C. or lower, in the slag T.V. calculated by the formula (1). A method for dephosphorizing hot metal, which comprises controlling a top-blown acid flow rate, a bottom-blown gas flow rate, and a top-blown lance height so that the Fe concentration is 10 to 20% by weight. T. in slag Fe concentration (wt%) = 6.49 × (the top-blown oxygen-flow-rate) (Nm 3 / min / t ) -5.73 × ( bottom blowing agitation power) (kW / t) -15.35 × (L / L O) +9.68 │2-CaO / SiO 2 │ + 11.73 (1) L: Depth of molten steel by top-blown jet L O : Depth of stationary molten steel
JP00850695A 1995-01-23 1995-01-23 Hot metal dephosphorization method Expired - Fee Related JP3345677B2 (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2820437A1 (en) * 2001-02-08 2002-08-09 Nippon Steel Corp LIQUID CAST DEPHOSPHORATION PROCESS
JP2002322506A (en) * 2001-04-23 2002-11-08 Nippon Steel Corp Converter dephosphorization of hot metal
JP2005206898A (en) * 2004-01-23 2005-08-04 Kobe Steel Ltd Converter operating method
JP2011058053A (en) * 2009-09-10 2011-03-24 Kobe Steel Ltd Dephosphorizing method
JP2011058052A (en) * 2009-09-10 2011-03-24 Kobe Steel Ltd Dephosphorizing method
JP2011102412A (en) * 2009-11-10 2011-05-26 Kobe Steel Ltd Dephosphorizing method using decarburized slag
CN102230052A (en) * 2011-07-19 2011-11-02 莱芜钢铁股份有限公司 Top-bottom combined blowing converter technology for high-carbon low-phosphor molten steel with single-slag process
JP2016145405A (en) * 2015-01-29 2016-08-12 Jfeスチール株式会社 Method for refining molten iron, method for analyzing composition of high-temperature material, and apparatus for analyzing composition of high-temperature material

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0770626A (en) * 1993-07-05 1995-03-14 Nippon Steel Corp Converter steelmaking

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0770626A (en) * 1993-07-05 1995-03-14 Nippon Steel Corp Converter steelmaking

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2820437A1 (en) * 2001-02-08 2002-08-09 Nippon Steel Corp LIQUID CAST DEPHOSPHORATION PROCESS
JP2002322506A (en) * 2001-04-23 2002-11-08 Nippon Steel Corp Converter dephosphorization of hot metal
JP2005206898A (en) * 2004-01-23 2005-08-04 Kobe Steel Ltd Converter operating method
JP2011058053A (en) * 2009-09-10 2011-03-24 Kobe Steel Ltd Dephosphorizing method
JP2011058052A (en) * 2009-09-10 2011-03-24 Kobe Steel Ltd Dephosphorizing method
JP2011102412A (en) * 2009-11-10 2011-05-26 Kobe Steel Ltd Dephosphorizing method using decarburized slag
CN102230052A (en) * 2011-07-19 2011-11-02 莱芜钢铁股份有限公司 Top-bottom combined blowing converter technology for high-carbon low-phosphor molten steel with single-slag process
JP2016145405A (en) * 2015-01-29 2016-08-12 Jfeスチール株式会社 Method for refining molten iron, method for analyzing composition of high-temperature material, and apparatus for analyzing composition of high-temperature material

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