Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPH0660340B2 - Desiliconization and dephosphorization treatment method of hot metal - Google Patents
[go: Go Back, main page]

JPH0660340B2 - Desiliconization and dephosphorization treatment method of hot metal - Google Patents

Desiliconization and dephosphorization treatment method of hot metal

Info

Publication number
JPH0660340B2
JPH0660340B2 JP2014389A JP2014389A JPH0660340B2 JP H0660340 B2 JPH0660340 B2 JP H0660340B2 JP 2014389 A JP2014389 A JP 2014389A JP 2014389 A JP2014389 A JP 2014389A JP H0660340 B2 JPH0660340 B2 JP H0660340B2
Authority
JP
Japan
Prior art keywords
hot metal
blowing
dephosphorization
gas
treatment
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.)
Expired - Lifetime
Application number
JP2014389A
Other languages
Japanese (ja)
Other versions
JPH02200717A (en
Inventor
進 務川
義正 水上
修平 小野山
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
Original Assignee
Nippon 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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP2014389A priority Critical patent/JPH0660340B2/en
Publication of JPH02200717A publication Critical patent/JPH02200717A/en
Publication of JPH0660340B2 publication Critical patent/JPH0660340B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

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

Description

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

〔産業上の利用分野〕 本発明は、溶銑の脱珪、脱りんを殆ど同時に行う処理方
法に関する。 〔従来の技術〕 従来溶銑の予備処理段階において、脱珪,脱りん処理を
一つの反応容器内で行う場合には、スラグの塩基度CaO
/SiO2を2つ程度とし、脱りん後のスラグに含まれる酸
化鉄中の全鉄分(以下これをT−Feと略称する)を10%
前後として脱りんしているが、脱りん後のりん分配比を
向上して、より低濃度のりんを得るため、またはより低
塩基度即ちより少ない生石灰原単位で脱りんを行うため
に、常に過剰の酸素を供給して(T−Fe)が低下するの
を防ぐようにしていた。 〔発明が解決しようとする課題〕 ところでこの方法では、相応の脱炭反応が進展して、後
工程の転炉精錬でのスクラップ溶解に必要な熱量を確保
できず、鉄歩留りが低下し、またスラグ中のFeOが高い
ままで操業するので、耐火物の損耗が大きくなるという
問題点があった。 本発明は、上記問題点に鑑みなされたもので、耐火物損
耗の少ない脱珪、脱りん処理、低濃度りんとする脱珪、
脱珪りん処理、または副原料節減を図る脱珪、脱りん処
理方法を提供する。
[Field of Industrial Application] The present invention relates to a treatment method of performing desiliconization and dephosphorization of hot metal almost at the same time. [Prior Art] When performing desiliconization and dephosphorization in a single reaction vessel in the conventional hot metal pretreatment stage, the slag basicity CaO
/ SiO 2 is about 2 and the total iron content in iron oxide contained in the slag after dephosphorization (hereinafter abbreviated as T-Fe) is 10%.
Although it is dephosphorized before and after, in order to improve the phosphorus distribution ratio after dephosphorization to obtain a lower concentration of phosphorus, or to perform dephosphorization with a lower basicity, that is, with a smaller amount of quicklime basic unit, it is always necessary. Excess oxygen was supplied to prevent (T-Fe) from decreasing. [Problems to be solved by the invention] By the way, in this method, a corresponding decarburization reaction progresses, the amount of heat necessary for melting scrap in the post-process converter smelting cannot be secured, and the iron yield decreases, and Since the FeO in the slag is operated while it is still high, there is a problem that the wear of the refractory becomes large. The present invention has been made in view of the above problems, desiliconization with less wear of refractory materials, dephosphorization treatment, desiliconization with low phosphorus concentration,
Provided are a method for removing silicon and phosphorus, or a method for removing silicon and phosphorus for the purpose of saving auxiliary materials.

【問題を解決するための手段】[Means for solving the problem]

本発明は、溶銑にCaO含有物質および酸素源を添加して
溶銑の脱珪、脱りんを行うに際し、所定量の酸素ガスを
溶銑に吹付けながら、下記(1)式にて定義される底吹
き攪拌力:1.2〜10KW/tを溶銑に与え、処理後のス
ラグに含まれる酸化鉄中の全鉄分を2.5〜4%とするこ
とを特徴とする溶銑の脱珪、脱りん処理方法、及び溶銑
にCaO含有物質および酸素源を添加して溶銑の脱珪、脱
りん処理を行うに際し、所定量の酸素ガスを溶銑に吹付
けながら、下記(1)式にて定義される溶銑に与える底
吹き攪拌力を、上記処理の初期には1.2〜10KW/tと
し、処理末期には0.5〜1.1KW/tに保つことを特徴とす
る溶銑の脱珪、脱珪りん処理方法である。 ここにQg;吹き込みガス量(Nl/min)、 T;溶銑温度(゜K)、 Wm;溶銑重量(t)、 Ho;吹き込み深さ(m)、 Tg;吹き込み前のガス温度(゜K) である。 〔作用〕 本発明は、酸素を供給しつつCaO系フラックスにより脱
珪・脱りん処理をおこなうに際し、攪拌力を1.2〜10K
W/tに保つことにより、スラグ中に含まれる酸化鉄中
の全鉄分(以下これをT−Feと略称する)が2.5〜4%
でも、当初りん含有量0.1%の溶銑をCaO原単位13.5kg/
t程度でこれを0.015%までに脱りん可能であることを
見出した。 その基本となる原理は次の如くである。 一般に、溶銑の脱りん反応は、次の3つの過程からな
る。 溶銑中のりんの物質移動 スラグ−溶銑界面におけるりんの酸化反応 スラグ中のPO4 3-の物質移動 ここで上記の酸化反応は、(イ)スグラ−溶銑界面の酸
素ポテンシャルが高い程、(2)スラグの塩基度が高い程
速やかに進行する。一方末脱珪溶銑を脱りんするに当っ
ては、スラグ塩基度は2程度と低いため、上記(イ)の効
果によって脱りんをおこなう。すなわちスラグの(T−
Fe)を10%程度に確保することにより、スラグの脱りん
能を確保する。 上記溶銑の脱りんの原理を踏まえて、溶銑を脱珪、脱り
ん処理する際に、所定の酸素ガスを溶銑に吹付けなが
ら、溶銑の底吹き攪拌力を1.2〜10KW/tに保てば、
処理後のスラグに含まれるT−Feを2.5〜4%とするこ
とができ、且つ充分な脱りんをし得ることを見出した。 溶銑へ所定量の酸素ガスを吹付けながら、底吹きCaCO3
から生成するCOガスあるいはCO2ガスで強攪拌すると、
酸素ガスの吹付けによって、FeOを生成し、溶銑中の珪
素が酸化されてSiO2を生成し、投入等の手段で添加した
CaO系フラックスとでの接触効率が高まり滓化が進行す
る。同時に上記強攪拌によって、スラグ−溶銑界面には
順次、溶銑とFeOが供給されているのでスラグ−溶銑界
面の酸素ポテンシャルが高く保たれることにより溶銑中
の珪素と平行してりんが早い時点で効率よく酸化される
ものである。これらのことより、処理後における溶銑の
りん含有量を0.015%程度まで低減させ得ることを可能
としたものである。 上記溶銑の攪拌力が1.2KW/t未満では、酸素ガスの供
給に対して攪拌力が弱くなり、スラグ中のFeOが増加す
る。また、攪拌力が10KW/t超になると、攪拌力が強す
ぎてスプラッシュが多量に発生し、Fe分のロスが増加し
て好ましくない。 次に、溶銑の一層のりんの低減を行うためには、脱りん
の停滞する処理の末期の酸素ポテンシャルが高く保つ必
要がある。これを達成する手段としてはスラグの還元を
遅くするように脱りん末期の攪拌力を落とすことで達成
できることを見出した。この手段と組合みわせて通常手
段として用いられている、酸素ガスの吹き付け量あるい
は酸化鉄の投入量を調整する手段に平行して実行するこ
とができ、具体的には酸素ガスの吹付け量を少なく(ソ
フトブロー)してFeOの生成を促進することが望まし
い。 次にCaO原単位の削減を行う作業を実行するためには、C
aO系フラックスの投入量を2乃至3割程度減少して、塩
基度を例えば1.8程度まで下げても、上記同様に脱りん
末期の攪拌力を落とすことで酸素ポテンシャルを高く保
つことにより、例えば、りん濃度を0.018%程度まで低
減できることを見出した。 上記脱りん末期の溶銑の量の攪拌力が0.5KW/t未満で
は、酸素ガスの供給に対して攪拌力が弱くなり、スラグ
中のFeOが増加する。また、攪拌力が1.1KW/t超になる
と、脱炭反応の進行によって酸素ガス消費量が増し、必
要なFeO量が確保し難くなる。 〔実施例〕 本発明の実施例を図面に基づいて説明する。 第1図は精錬装置の側断面図であり、この装置を使用し
て先ず160tの溶銑2と5tのスクラッシュ3を精錬容
器1に装入する。ついで塊状のCaO,塊状のCaF2,鉄鉱
石の混合物よりなる脱りんフラックスをホッパー6より
投入し、同時にブロータンク5内の脱りんフラックスを
N2ガスとともに底吹き羽口4より溶銑2中へ吹き込むと
ともに、ランス7を介して酸度ジェットを溶銑2に吹き
つける。 表1は本発明による実施例1、2、3と比較例の精錬条
件を示し、また第2図に実施例1、第3図に実施例2、
第4図に実施例3、第5図に比較例のそれぞれの溶銑成
分の経過変化を示す。 実施例1においては、CaO原単位17.5Kg/tにてりん濃
度は0.017%に低下し、また実施例2においては同様に
原単位12.1Kg/tにて0.018%に低下した。実施例3に
おいては、CaO原単位18.1Kg/tにてりん濃度は0.017%
である。また、脱りん後のスラグに含まれるT−Feを3.
7%に低減でき処理炉の耐火物の損耗を低減できる。こ
れに対して比較例においては、CaO原単位は実施例3と
同程度の18.0Kg/tであったが、攪拌力が弱く、処理後
のりん濃度は0.024%止まりであった。 このように本発明においては、脱珪処理を施していない
溶銑のりん濃度を少いCaO量にて容易に0.01%以下に低
減可能とするものである。 本発明は、攪拌力を調整する機構を有しておれば、すべ
ての精錬容器にて容易に適用可能であり、また攪拌力を
0.5〜1.1KW/tに低下させるのは、脱りん処理終了前の
3〜4分程度でよい。また攪拌を与える手段としては、
Ar,N2等のガスまたはCaCO3等のガス発生物質を、ランス
または羽口を介して吹き込むことによっても達成され
る。 〔発明の効果〕 以上説明した如く本発明は、溶銑に与える攪拌力を調整
することにより、フラックス等を余分に投入することな
く、スラグの脱りん能を確保して反応を促進させるもの
であり、少ない副原料でもって低脱りんを達成すること
ができ、原料費の節減と予備処理の効率化を図り得る。
The present invention, when a CaO-containing substance and an oxygen source are added to hot metal to desiliconize and dephosphorize the hot metal, while spraying a predetermined amount of oxygen gas to the hot metal, the bottom defined by the following formula (1) Blowing stirring power: 1.2 to 10 KW / t is given to the hot metal, and the total iron content in the iron oxide contained in the slag after the treatment is 2.5 to 4%, and a method for desiliconizing and dephosphorizing the hot metal, and When adding a CaO-containing substance and an oxygen source to the hot metal to perform desiliconization and dephosphorization treatment of the hot metal, the bottom to be given to the hot metal defined by the following formula (1) while spraying a predetermined amount of oxygen gas to the hot metal This is a method for desiliconizing and desiliconizing phosphorus of hot metal, characterized in that the blowing stirring power is kept at 1.2 to 10 KW / t at the beginning of the above treatment and kept at 0.5 to 1.1 KW / t at the end of the treatment. Here, Qg: blowing gas amount (Nl / min), T: hot metal temperature (° K), Wm: hot metal weight (t), Ho: blowing depth (m), Tg: gas temperature before blowing (° K) Is. [Operation] The present invention, when performing desiliconization and dephosphorization treatment by CaO-based flux while supplying oxygen, stirring force 1.2 ~ 10K
By maintaining W / t, the total iron content in iron oxide contained in slag (hereinafter abbreviated as T-Fe) is 2.5 to 4%.
However, the initial content of hot metal with a phosphorus content of 0.1% was 13.5 kg / CaO.
It was found that this can be dephosphorized up to 0.015% at about t. The basic principle is as follows. Generally, the dephosphorization reaction of hot metal consists of the following three processes. Phosphorus mass transfer slag in molten iron - above oxidation reaction PO 4 3- of mass transfer, where the oxidation reaction in the slag of phosphorus in molten iron interface, (b) Sugura - higher oxygen potential of the molten iron surface, (2 ) The higher the basicity of the slag, the faster the progress. On the other hand, in dephosphorizing the undesiliconized hot metal, since the slag basicity is as low as about 2, dephosphorization is performed by the effect of the above (a). That is, the slag (T-
By securing Fe) to about 10%, the dephosphorization ability of slag is secured. Based on the above principle of dephosphorization of hot metal, when desiliconizing and dephosphorizing the hot metal, it is necessary to keep the bottom blowing stirring power of the hot metal at 1.2 to 10 KW / t while spraying a predetermined oxygen gas to the hot metal. ,
It was found that T-Fe contained in the slag after the treatment can be 2.5 to 4% and sufficient dephosphorization can be performed. While blowing a predetermined amount of oxygen gas onto the hot metal, bottom-blown CaCO 3
When strong stirring with CO gas or CO 2 gas generated from
By spraying oxygen gas, FeO was generated, silicon in the hot metal was oxidized to generate SiO 2, and it was added by means such as charging.
The contact efficiency with CaO-based flux increases and the slag formation progresses. At the same time, by the above-mentioned strong stirring, the hot metal and FeO are sequentially supplied to the slag-hot metal interface, so that the oxygen potential at the slag-hot metal interface is kept high, so that phosphorus in parallel with the silicon in the hot metal is early. It can be efficiently oxidized. From these facts, the phosphorus content of the hot metal after the treatment can be reduced to about 0.015%. When the stirring power of the hot metal is less than 1.2 KW / t, the stirring power becomes weak against the supply of oxygen gas, and FeO in the slag increases. Further, if the stirring power exceeds 10 KW / t, the stirring power is too strong, a large amount of splash is generated, and the loss of Fe content increases, which is not preferable. Next, in order to further reduce phosphorus in the hot metal, it is necessary to keep the oxygen potential high at the final stage of the treatment in which dephosphorization is stagnant. It was found that the means for achieving this can be achieved by reducing the stirring power at the final stage of dephosphorization so as to delay the reduction of slag. It can be carried out in parallel with the means for adjusting the amount of oxygen gas sprayed or the amount of iron oxide charged, which is usually used in combination with this means, and specifically, the amount of oxygen gas sprayed. It is desirable to reduce the amount (soft blow) to promote the generation of FeO. Next, in order to carry out the work of reducing the CaO intensity, C
Even if the amount of aO-based flux input is reduced by 20 to 30% and the basicity is lowered to, for example, about 1.8, the stirring power at the final stage of dephosphorization is reduced in the same manner as described above to maintain a high oxygen potential. It was found that the phosphorus concentration can be reduced to about 0.018%. When the stirring power of the amount of hot metal at the final stage of dephosphorization is less than 0.5 KW / t, the stirring power becomes weak with respect to the supply of oxygen gas, and FeO in the slag increases. Further, when the stirring power exceeds 1.1 KW / t, the oxygen gas consumption increases due to the progress of the decarburization reaction, and it becomes difficult to secure the necessary FeO amount. [Embodiment] An embodiment of the present invention will be described with reference to the drawings. FIG. 1 is a side sectional view of a refining apparatus. Using this apparatus, first, 160 t of hot metal 2 and 5 t of slash 3 are charged into a refining vessel 1. Then, a dephosphorization flux composed of a mixture of massive CaO, massive CaF 2 , and iron ore was charged from the hopper 6, and at the same time, the dephosphorization flux in the blow tank 5 was changed.
It is blown into the hot metal 2 from the bottom blowing tuyere 4 together with the N 2 gas, and an acidity jet is blown to the hot metal 2 through the lance 7. Table 1 shows refining conditions of Examples 1, 2 and 3 according to the present invention and a comparative example, and FIG. 2 shows Example 1 and FIG. 3 shows Example 2.
FIG. 4 shows the changes over time in the hot metal components of Example 3 and FIG. 5, respectively. In Example 1, the phosphorus concentration decreased to 0.017% at the CaO basic unit of 17.5 Kg / t, and similarly in Example 2, the phosphorus concentration decreased to 0.018% at the 12.0 Kg / t basic unit. In Example 3, the CaO basic unit is 18.1 kg / t and the phosphorus concentration is 0.017%.
Is. Also, T-Fe contained in the slag after dephosphorization is 3.
It can be reduced to 7% and wear of refractory in the processing furnace can be reduced. On the other hand, in the comparative example, the CaO basic unit was 18.0 kg / t, which was the same level as in Example 3, but the stirring power was weak and the phosphorus concentration after the treatment was 0.024%. As described above, the present invention makes it possible to easily reduce the phosphorus concentration of hot metal not subjected to desiliconization treatment to 0.01% or less with a small amount of CaO. The present invention can be easily applied to all refining vessels as long as it has a mechanism for adjusting the stirring force.
The reduction to 0.5 to 1.1 KW / t is sufficient for about 3 to 4 minutes before the completion of the dephosphorization treatment. Further, as a means for giving stirring,
It is also achieved by blowing a gas such as Ar or N 2 or a gas generating substance such as CaCO 3 through a lance or a tuyere. [Advantages of the Invention] As described above, the present invention is to adjust the stirring force applied to the hot metal to secure the dephosphorization ability of the slag and promote the reaction without adding extra flux or the like. In addition, low dephosphorization can be achieved with a small amount of auxiliary raw material, and the raw material cost can be reduced and pretreatment efficiency can be improved.

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

第1図は精錬装置の一例を示す側断面図、第2図、第3
図及び第4図は実施例における溶鉄成分の経過変化を示
すグラフ。第5図は比較例における経時変化を示すグラ
フ。 1……精錬容器、2……溶銑、3……スクラップ、4…
…底吹き羽口、5……ブロータンク、6……ホッパー、
7……ランス
FIG. 1 is a side sectional view showing an example of a refining apparatus, FIG. 2 and FIG.
FIG. 4 and FIG. 4 are graphs showing changes over time in molten iron components in the examples. FIG. 5 is a graph showing changes with time in the comparative example. 1 ... Refining container, 2 ... Hot metal, 3 ... Scrap, 4 ...
… Bottom blowing tuyere, 5 …… blow tank, 6 …… hopper,
7 ... Lance

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】溶銑にCaO含有物質および酸素源を添加し
て溶銑の脱珪、脱りん処理を行うに際し、所定量の酸素
ガスを溶銑に吹付けながら、下記(1)式にて定義され
る底吹き攪拌力を1.2〜10KW/tを溶銑に与え、処理
後のスラグに含まれる酸化鉄中の全鉄分を2.5〜4%と
することを特徴とする溶銑の脱珪、脱りん処理方法。 ここにQg;吹き込みガス量(Nl/min)、 T;溶銑温度(゜K)、 Wm;溶銑重量(t)、 Ho;吹き込み深さ(m)、 Tg;吹き込み前のガス温度(゜K)
1. When a CaO-containing substance and an oxygen source are added to hot metal to perform desiliconization and dephosphorization treatment of hot metal, a predetermined amount of oxygen gas is sprayed onto the hot metal as defined by the following formula (1). A method for desiliconizing and dephosphorizing hot metal, characterized in that a bottom blowing stirring power of 1.2 to 10 KW / t is given to the hot metal and the total iron content in iron oxide contained in the slag after the treatment is 2.5 to 4%. . Here, Qg: blowing gas amount (Nl / min), T: hot metal temperature (° K), Wm: hot metal weight (t), Ho: blowing depth (m), Tg: gas temperature before blowing (° K)
【請求項2】溶銑にCaO含有物質および酸素源を添加し
て溶銑の脱珪、脱りん処理を行うに際し、所定量の酸素
ガスを溶銑に吹付けながら、下記(1)式にて定義され
る溶銑に与える底吹き攪拌力を、上記処理の初期には
1.2〜10KW/tとし、処理末期には0.5〜1.1KW/tに保
つことを特徴とする溶銑の脱珪、脱りん処理方法。 ここにQg;吹き込みガス量(Nl/min)、 T;溶銑温度(゜K)、 Wm;溶銑重量(t)、 Ho;吹き込み深さ(m)、 Tg;吹き込み前のガス温度(゜K)
2. When a CaO-containing substance and an oxygen source are added to the hot metal to perform desiliconization and dephosphorization treatment of the hot metal, a predetermined amount of oxygen gas is sprayed onto the hot metal, and is defined by the following formula (1). The bottom blowing agitation force given to the hot metal is
A method of desiliconizing and dephosphorizing hot metal, which is characterized by maintaining 1.2 to 10 kW / t and maintaining 0.5 to 1.1 kW / t at the end of treatment. Here, Qg: blowing gas amount (Nl / min), T: hot metal temperature (° K), Wm: hot metal weight (t), Ho: blowing depth (m), Tg: gas temperature before blowing (° K)
JP2014389A 1989-01-30 1989-01-30 Desiliconization and dephosphorization treatment method of hot metal Expired - Lifetime JPH0660340B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2014389A JPH0660340B2 (en) 1989-01-30 1989-01-30 Desiliconization and dephosphorization treatment method of hot metal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2014389A JPH0660340B2 (en) 1989-01-30 1989-01-30 Desiliconization and dephosphorization treatment method of hot metal

Publications (2)

Publication Number Publication Date
JPH02200717A JPH02200717A (en) 1990-08-09
JPH0660340B2 true JPH0660340B2 (en) 1994-08-10

Family

ID=12018924

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014389A Expired - Lifetime JPH0660340B2 (en) 1989-01-30 1989-01-30 Desiliconization and dephosphorization treatment method of hot metal

Country Status (1)

Country Link
JP (1) JPH0660340B2 (en)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62109913A (en) * 1985-11-06 1987-05-21 Kobe Steel Ltd Desiliconizing and dephosphorizing method for molten iron
JPS62109911A (en) * 1985-11-06 1987-05-21 Kobe Steel Ltd Desiliconizing and dephosphorizing method for molten iron
JPS63195209A (en) * 1987-02-07 1988-08-12 Sumitomo Metal Ind Ltd Steel making method
JPH075953B2 (en) * 1987-04-17 1995-01-25 日新製鋼株式会社 Improved hot metal dephosphorization method.

Also Published As

Publication number Publication date
JPH02200717A (en) 1990-08-09

Similar Documents

Publication Publication Date Title
JPS6123245B2 (en)
JPH11158526A (en) Method for producing high P slag
JP2006274349A (en) Steel refining method
JP2001288507A (en) Manufacturing method of low phosphorus hot metal
JP2019151535A (en) Method of producing phosphate slag fertilizer
JPH0660340B2 (en) Desiliconization and dephosphorization treatment method of hot metal
JP2001049320A (en) Steelmaking method using high phosphate ore as raw material
JP3823595B2 (en) Hot metal refining method
JPH0660341B2 (en) Method of dephosphorization and desulfurization of hot metal
JP2004010935A (en) Manufacturing method of molten steel
JPS62170409A (en) Preliminary treatment of molten iron
JPS62109911A (en) Desiliconizing and dephosphorizing method for molten iron
JP2002322506A (en) Converter dephosphorization of hot metal
JPH0660339B2 (en) Method of desiliconizing and dephosphorizing hot metal
JPS6247417A (en) Melt refining method for scrap
JPH09176717A (en) Steelmaking method for blast furnace hot metal
JP2001207206A (en) Method for dephosphorizing molten iron
JP2009249666A (en) Dephosphorization refining method for molten iron
JP2802799B2 (en) Dephosphorization and desulfurization method for crude molten stainless steel and flux used for it
JP3898964B2 (en) Dephosphorization method for hot metal
JP2002256326A (en) Refining method of molten iron
JPH068454B2 (en) Dephosphorization / desulfurization method of molten iron alloy containing chromium
JPS61104014A (en) Method for reducing mn ore with high efficiency in oxidation refining furnace
JP2002212616A (en) Control method of hot metal dephosphorization
JP4026447B2 (en) Method for producing low phosphorus hot metal

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080810

Year of fee payment: 14

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090810

Year of fee payment: 15

EXPY Cancellation because of completion of term
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090810

Year of fee payment: 15