JP3440755B2 - How to add auxiliary raw materials to the converter - Google Patents

How to add auxiliary raw materials to the converter

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Publication number
JP3440755B2
JP3440755B2 JP15496897A JP15496897A JP3440755B2 JP 3440755 B2 JP3440755 B2 JP 3440755B2 JP 15496897 A JP15496897 A JP 15496897A JP 15496897 A JP15496897 A JP 15496897A JP 3440755 B2 JP3440755 B2 JP 3440755B2
Authority
JP
Japan
Prior art keywords
slag
blowing
converter
period
hot metal
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 - Fee Related
Application number
JP15496897A
Other languages
Japanese (ja)
Other versions
JPH116006A (en
Inventor
俊史 安部
治志 奥田
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
JFE Steel Corp
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Filing date
Publication date
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Priority to JP15496897A priority Critical patent/JP3440755B2/en
Publication of JPH116006A publication Critical patent/JPH116006A/en
Application granted granted Critical
Publication of JP3440755B2 publication Critical patent/JP3440755B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、転炉への副原料投
入方法に関し、特に、予備処理後の溶銑を転炉で精錬す
るに際し、使用する多種の造滓剤のうちから適切なもの
を、適切な時期に適切な量だけ転炉へ投入し、それらの
滓化を円滑、且つ安定して行う技術である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for charging an auxiliary raw material into a converter, and more particularly, to a suitable slag forming agent used in refining hot metal after pretreatment in the converter. It is a technology that puts an appropriate amount into a converter at an appropriate time to smoothly and stably slag them.

【0002】[0002]

【従来の技術】近年の転炉製鋼では、酸素上吹き機能に
加え、炉底から酸素、窒素、CO,CO2 、あるいはア
ルゴン・ガスを吹込む機能を備えた所謂複合転炉が一般
に用いられるようになった。この複合転炉は、脱炭速度
を向上させ、それに伴って酸素使用量の低減をもたらし
た。そして、この優れた脱炭特性をさらに高める観点か
ら、予め脱珪、脱硫、脱燐処理(以下、予備処理とい
う)を施した溶銑を使用すれば、転炉の負荷が軽減し、
上記効果が一層向上することが期待された。そのため、
最近の転炉製鋼では、使用する溶銑のうちの90%が予
備処理を施され、所謂脱燐銑を用いての吹錬が多くなっ
ている。
2. Description of the Related Art In recent years, in converter steelmaking, a so-called composite converter having a function of blowing oxygen, nitrogen, CO, CO 2 , or argon gas from the bottom of the furnace is generally used in addition to the function of blowing oxygen upward. It became so. This combined converter increased the decarburization rate and, consequently, reduced the oxygen usage. Then, from the viewpoint of further enhancing this excellent decarburization property, if the hot metal that has been previously subjected to desiliconization, desulfurization, and dephosphorization treatment (hereinafter referred to as pretreatment) is used, the load on the converter is reduced,
It was expected that the above effects would be further improved. for that reason,
In the recent converter steelmaking, 90% of the hot metal used is subjected to a pretreatment, and so-called dephosphorization hot-melting is often used.

【0003】ところで、脱燐銑は、予備処理を施してい
ない通常の溶銑に比べ、転炉吹錬における初期滓化が遅
いという問題がある。溶銑中のSi含有量も低いので、
初期滓化の核となるSiO2 の生成量が少ないからであ
る。そのため、現在の転炉操業では、造滓剤(以下、副
原料ともいう)を過剰に投入し、必要以上の脱燐を行っ
てしまう傾向にある。
By the way, dephosphorization pig iron has a problem in that the initial slag formation in the converter blowing is slower than that of ordinary hot metal which is not pretreated. Since the Si content in the hot metal is low,
This is because the amount of SiO 2 that forms the nucleus of initial slag formation is small. Therefore, in the present converter operation, there is a tendency that the slag forming agent (hereinafter, also referred to as an auxiliary material) is excessively added to dephosphorize more than necessary.

【0004】また、現在の転炉操業では、転炉耐火物の
溶損防止の観点から、出鋼時の数回に1回は、スラグの
一部を転炉に残留させ、それに軽焼ドロマイトを加えて
転炉を傾動させる所謂スラグ・コーティングを行ってい
る。従って、このスラグ残しの有無が、初期滓化に重要
な影響を与え、チャージ毎の滓化にバラツキを起こすと
いう別の問題もある。なお、軽焼ドロマイトを加えるの
は、転炉耐火物(MgO系)の溶損防止にとり、吹錬中
はスラグが常にMgO過飽和であることが必要なためで
ある。
Further, in the present converter operation, from the viewpoint of preventing melting damage of the converter refractory, a part of the slag is left in the converter once every several times during tapping, and light burned dolomite is added to the slag. So-called slag coating for tilting the converter is added. Therefore, there is another problem that the presence or absence of the slag left behind has an important influence on the initial slag formation, and the slag formation varies from charge to charge. The reason for adding the light-burned dolomite is that the slag must be constantly supersaturated with MgO during blowing in order to prevent melting of the converter refractory (MgO-based).

【0005】さらに、現在の転炉操業では、図6に示す
ように、溶鋼5を覆うスラグ6の絶対量が少ないので、
吹錬中に溶鋼の所謂スピッティング9が起こったり、ダ
スト10を発生させ易い傾向もある。このスピッティン
グ9は、転炉1内での地金付き8を大にして溶鋼ロスを
増大させ、ダスト発生も同様の意味があるので、適正な
滓化とスラグ量の確保は、転炉操業にとって重要な課題
となっている。
Further, in the present converter operation, as shown in FIG. 6, since the absolute amount of the slag 6 covering the molten steel 5 is small,
There is also a tendency that so-called spitting 9 of molten steel occurs or dust 10 is easily generated during blowing. This spitting 9 increases the molten steel loss by increasing the size of the ingot 8 in the converter 1, and dust generation has the same meaning. Therefore, proper slagging and securing of the amount of slag are required in the converter operation. Has become an important issue for

【0006】[0006]

【発明が解決しようとする課題】本発明は、かかる事情
を鑑み、転炉吹錬の初期から迅速滓化を円滑に行い、転
炉耐火物の溶損防止、スピッティングとダストの発生抑
制による溶銑歩留の向上を図る転炉への副原料投入方法
を提供することを目的としている。
SUMMARY OF THE INVENTION In view of such circumstances, the present invention is intended to smoothly perform rapid slag formation from the initial stage of converter blowing, prevent meltdown of converter refractory, and suppress spitting and dust generation. It is an object of the present invention to provide a method for feeding auxiliary raw materials to a converter for improving the hot metal yield.

【0007】[0007]

【課題を解決するための手段】発明者は、上記目的を達
成するため、従来から行われている転炉への副原料の投
入方法を、平衡論に基づき造滓剤の組成から融点を計算
するソフト(ChemSageと呼ばれて市販され、投
入する各副原料の化学組成から多元系平衡状態図を計算
で求めるものである)を用いた解析と、多数の実験とを
繰り返して、見直した。そして、その成果を本発明とし
て具現化した。
In order to achieve the above object, the inventor has calculated the melting point from the composition of the slag-forming agent based on the equilibrium theory by the conventional method of charging the auxiliary raw material into the converter. It was reviewed by repeating an analysis using a software (which is called “ChemSage”, which is commercially available and which calculates the equilibrium diagram of a multi-component system from the chemical composition of each auxiliary material to be input) and a large number of experiments. And the result was materialized as this invention.

【0008】すなわち、本発明は、転炉内の溶銑に、焼
石灰、軽焼ドロマイト、生ドロマイト、蛇紋岩、造塊滓
及び蛍石を投入して滓化し、生じたスラグと溶銑間のス
ラグ−メタル反応を酸素吹錬下で行わせるに際し、全吹
錬時間の20%から60%の期間内に焼石灰を投入し、
且つその期間内で全投入焼石灰量を複数回に均等分割し
て投入すると共に、前記蛇紋岩は、上記焼石灰の投入期
間内で複数回に分割して投入し、前記蛍石は、全吹錬期
間の当初から30%までに投入し、前記軽焼ドロマイト
及び前記造塊滓は、全吹錬期間の当初から10%までに
投入し、前記生ドロマイトは、全吹錬期間の25%から
30%までに投入することを特徴とする転炉への副原料
投入方法である。
That is , according to the present invention, burnt lime, light burnt dolomite, raw dolomite, serpentine, ingot slag and fluorspar are put into molten pig iron in the converter to form slag, and the slag between the slag and the molten pig iron produced. -When the metal reaction is carried out under oxygen blowing, burnt lime is charged within 20% to 60% of the total blowing time,
And, during the period, the total amount of burnt lime added is equally divided into multiple times and the serpentine is added at the above-mentioned burnt lime loading period.
It is divided into several times and added during the period.
From the beginning of the period, put up to 30%, the light burned dolomite
And the above-mentioned slag will be used up to 10% from the beginning of the entire blowing period.
Inject the raw dolomite from 25% of the total blowing period
It is a method of charging auxiliary raw materials into a converter, which is characterized by charging up to 30% .

【0009】[0009]

【0010】らに加えて、本発明は、上記銑鉄を、予
備処理後の溶銑とすることを特徴とする転炉への副原料
投入方法でもある。本発明では、転炉への副原料の投入
を上記の構成で行うようにしたので、転炉吹錬の初期か
ら迅速滓化が円滑に行なえるようになる。その結果、転
炉耐火物の溶損防止、スピッティングとダストの発生抑
制による溶銑歩留の向上ばかりでなく、使用する副原料
量や合金鉄量の削減も可能となった。
In addition to the of al, the present invention, the pig iron, is also a sub-material injection method to the converter, characterized in that the hot metal after the pretreatment. In the present invention, since the auxiliary raw material is charged into the converter with the above-described configuration, rapid slaging can be smoothly performed from the initial stage of the blowing of the converter. As a result, not only was it possible to improve the hot metal yield by preventing melting damage of converter refractories and suppressing the generation of spitting and dust, but it was also possible to reduce the amount of auxiliary raw materials and the amount of ferroalloy used.

【0011】[0011]

【発明の実施の形態】以下に、発明をなすに至る経緯も
含め、本発明の内容を説明する。従来、転炉吹錬におけ
る副原料の投入は、200トン転炉を代表例として示す
と、図2のように行われている(投入タイミングを▼マ
ークで示す)。すなわち、全吹錬時間を10分割して%
で表示するが、 焼石灰: 5〜50%の期間内で分割投入、一
回当たりの投入基準量500kg 軽焼ドロマイト: 吹錬当初から15%までの期間、
0.7トン/分で連続投入 生ドロマイト: 25%から35%の期間、0.7ト
ン/分で連続投入 蛇紋岩: 吹錬当初から40%の期間までに投
入終了 造塊剤: 全量事前秤量で当初に一括投入 蛍石: 10〜80%の期間に分割投入、一
回当たりの投入基準量150kg これを脱燐溶銑の吹錬に適用した場合の前記Chem
Sageでの解析結果を表1に示す。また、CaO溶解
度(CaOの滓化率R’ともいう)(%)の吹錬中の推
移を図3に示す。
BEST MODE FOR CARRYING OUT THE INVENTION The contents of the present invention will be described below, including the process leading to the invention. 2. Description of the Related Art Conventionally, when a 200-ton converter is used as a typical example, the charging of the auxiliary raw material in the converter blowing is performed as shown in FIG. 2 (the charging timing is indicated by a mark). That is, the total blowing time is divided into 10%
It is indicated by: Burned lime: Split charging within a period of 5 to 50%, input standard amount of 500 kg per time Light burned dolomite: Period from the beginning of blowing to 15%,
Continuous dosing at 0.7 ton / min Raw dolomite: 25% to 35% period, Continuous dosing at 0.7 ton / min Serpentine rock: Finished by 40% period from the beginning of blowing Slagging agent: Full amount in advance Initially batch-injection by weighing: Fluorite: 10 to 80% dividedly injecting, reference amount of 150kg each time, when the above is applied for dephosphorization hot metal blowing, Chem
The results of the Sage analysis are shown in Table 1. Further, FIG. 3 shows a transition of CaO solubility (also referred to as CaO slagging ratio R ′) (%) during blowing.

【0012】表1及び図3より、この脱燐溶銑の吹錬で
は、R’は吹錬期間の60%を経過しても30%を下回
っている。つまり、投入した副原料中のCaO分の30
%以下しか溶解していない。しかも、これは計算結果で
あって、実際の吹錬ではもっと低いものと思われる。
From Table 1 and FIG. 3, in the blowing of this dephosphorized hot metal, R'is less than 30% even after 60% of the blowing period. That is, 30% of CaO in the input auxiliary material
% Or less is dissolved. Moreover, this is a calculation result, and it seems to be lower in actual blowing.

【0013】[0013]

【表1】 [Table 1]

【0014】また、吹止時に溶解しているCaOを10
0として、吹錬途中で溶解しているCaO量を求め、図
4に示す。図4より、吹錬初期(10〜30%)では、
吹止時の溶解CaOの35%程度が溶解の限界であるこ
とがわかる。つまり、その時期では、総CaO投入量の
約35%程度しか滓化していない。ところが、通常の実
操業では、事前投入の焼石灰を含めると、この時期まで
に総CaO投入量の70%が投入される。従って、従来
の操業では、吹錬初期でCaOが過剰投入になってい
る。
In addition, when CaO is dissolved at the time of blowing stop,
The amount of CaO dissolved in the course of blowing was determined as 0 and is shown in FIG. From FIG. 4, in the initial stage of blowing (10 to 30%),
It can be seen that about 35% of dissolved CaO at the time of blowing is the limit of dissolution. That is, at that time, only about 35% of the total CaO input has been slagged. However, in a normal operation, 70% of the total CaO input is added by this time, including the pre-added calcined lime. Therefore, in the conventional operation, CaO is excessively added at the initial stage of blowing.

【0015】そこで、発明者は、CaO分の適切な量を
適切な時期に投入することを鋭意試行し、前記の本発明
を完成させたのである。発明で、全吹錬時間の20%
から60%の期間内に焼石灰を投入するのは、20%未
満ではCaOが過剰投入になり、かえって生成したスラ
グの温度を低下し、滓化の障害となり、60%を超えて
投入すると、吹止時でも滓化せずに固体で残存するもの
があるからである。また、一回当たりの投入量は、40
0kg程度/溶鋼トンとし、複数回の分割投入が好まし
い。投入量と滓化速度がマッチングし、適切な滓化がで
きるからである。
[0015] Therefore, the inventors have conducted extensive attempt to put the appropriate amount of CaO content to the appropriate time, it was completed the previous Symbol present invention. In the present invention, 20% of the total blowing time
If less than 20%, CaO will be added excessively, and the temperature of the slag produced will be lowered, which will become an obstacle to slag formation, and if more than 60% is added, This is because there are some that remain solid without slagging even when blowing off. Moreover, the input amount per time is 40
Approximately 0 kg / ton of molten steel , it is preferable to divide and input multiple times.
Yes. This is because the input amount and the slagging speed match, and the slagging can be performed appropriately.

【0016】次に、上記CaOの溶解促進には、SiO
2 の共存が不可欠なことから蛇紋岩の添加方法を考え
た。できるだけ早く、スラグ−メタル反応に必要なスラ
グ組成にするためである。また、CaOやSiO2 の溶
解に際しては、できるだけ低い温度での溶解が、滓化促
進の観点から望ましい。そこで、本発明では、それらの
混合物の融点が低下するよう、蛍石を、全吹錬期間の当
初から30%までに投入して、焼石灰や蛇紋岩の溶解を
助けるベースとなるスラグを予め形成させておくように
した。さらに、スラグの融点は多成分系ほど低下するの
で、このベースとなるスラグの融点を下げるため、軽焼
ドロマイト、造塊滓を生全吹錬期間の当初から10%ま
でに投入するようにしたり、あるいは生ドロマイトも吹
錬の初期に投入するようにした。ここで、造塊滓とは、
取鍋から回収したスラグのことである。
Next, in order to accelerate the dissolution of CaO, SiO
Since the coexistence of 2 is indispensable, we considered a method of adding serpentinite.
It was This is to make the slag composition necessary for the slag-metal reaction as soon as possible. In addition, when CaO or SiO 2 is dissolved, it is desirable to dissolve it at a temperature as low as possible from the viewpoint of promoting slag formation. Therefore , in the present invention, in order to lower the melting point of the mixture, fluorite is added from the beginning of the entire blowing period up to 30%, and a slag serving as a base that aids in the dissolution of burnt lime and serpentine is previously prepared. I was allowed to form it. Furthermore, since the melting point of the slag decreases as the multi-component system, for lowering the melting point of the slag to be the base, dolomitic, the Zokatamarikasu so as to put into up to 10% from the initial raw whole blowing period Or, raw dolomite was also introduced at the beginning of blowing. Here, the ingot is
It is the slag collected from the ladle.

【0017】なお、軽焼ドロマイトや生ドロマイトは、
転炉の内張り耐火物がMgO系であるので、その溶損防
止の観点からも早期の滓化が好ましい。但し、生ドロマ
イトは、吹錬当初から投入しても冷却能が高いため、従
来どおりの全吹錬期間の25%から30%までに投入す
るようにした。この本発明に係る副原料投入方法の一例
をパターン化して図1に示す。すなわち、それは、下記
のように説明される。 焼石灰: 20〜0%の期間内で分割投入、
一回当たりの投入基準量400kg/溶鋼トン 軽焼ドロマイト: 吹錬当初から10%までの期間、
0.7トン/分で連続投入 生ドロマイト: 25%から30%の期間、0.7ト
ン/分で連続投入 蛇紋岩: 上記焼石灰の投入期間内で複数回に
分割投入 造塊剤: 全量事前秤量で当初から10%の時
期に投入 蛍石: 全吹錬期間の25%〜30%に投
入、一回当たりの投入基準量150kg 加えて、本発明としては、出鋼時のスラグ残しの有無に
応じて、投入する副原料の量を変更することも配慮し
た。つまり、出鋼時に全量排滓された後のチャージで
は、初期滓化でのスラグ組成がスラグ残しがあるチャー
ジでのものとは異なり、CaOの滓化遅れやバラツキ、
スラグ組成のバラツキ、脱燐不良やスラグ中MgOの未
飽和(耐火物溶損防止のためには、吹錬中は過飽和であ
ることが必須)が生じるからである。例えば、図5に、
スラグ残しの有無により、その後のチャージでのCaO
溶解度R’の違いを示しておく。
The light-burned dolomite and raw dolomite are
Since the refractory lining of the converter is MgO-based, early slagging is preferable from the viewpoint of preventing its melting loss. However, since the raw dolomite has a high cooling ability even when it is charged from the beginning of blowing, it was added from 25% to 30% of the total blowing period as usual. An example of a secondary raw material charging method according to the present invention this and is patterned shown in Fig. That is, it is described as follows. Roasted lime: divided input within a period of 20 to 60 %,
Input standard amount 400kg / ton of molten steel Light burned dolomite: Period from the beginning of blowing to 10%,
Continuous dosing at 0.7 ton / min Raw dolomite: 25% to 30% period, Continuous dosing at 0.7 ton / min Serpentine rock: Divided into multiple times within the above-mentioned burned lime loading period. Fluorite added at a time of 10% from the beginning by pre-weighing: Input at 25% to 30% of the total blowing period, reference amount of 150 kg per addition In addition, as the present invention, the slag remaining at the time of tapping Consideration was also given to changing the amount of auxiliary raw material to be input depending on the presence or absence. In other words, in the charge after the total amount of slag is discharged at the time of tapping, the slag composition in the initial slag formation is different from that in the charge in which slag remains, and CaO slag formation delay and variation,
This is because variations in the slag composition, poor dephosphorization, and unsaturation of MgO in the slag (supersaturation is essential during blowing to prevent refractory meltdown). For example, in FIG.
Depending on the presence or absence of slag left, CaO in the subsequent charge
The difference in solubility R'is shown.

【0018】そこで、かかる場合、スラグ残し後チャー
ジでの滓化の核に代わるものを、副原料で補う必要があ
。その際、スピッティング防止、耐火物保護の観点か
ら、スラグ中のAl23 を4wt%,初期塩基度を3
〜4とするように配慮している。
Therefore, in such a case, it is necessary to supplement the substitute for the core of slag formation in the charge after leaving the slag with an auxiliary material . During its, spitting prevented, in view of the refractory protective, the Al 2 O 3 in the slag 4 wt%, the initial basicity 3
Consideration is given to ~ 4.

【0019】 軽焼ドロマイト(kg/t)=焼石灰(kg/t)×
0.29 蛇紋岩(kg/t)=焼石灰(kg/t)×0.22 造塊滓(kg/t)=焼石灰(kg/t)×0.39 蛍石(kg/t)=焼石灰(kg/t)×0.12 さらに加えて、以上述べた本発明は、溶銑予備処理を経
ない通常の溶銑にも適用できるので、予備処理後の溶銑
を吹錬する場合を特に第2の本発明とした。
Light-burnt dolomite (kg / t) = calcined lime (kg / t) ×
0.29 Serpentine (kg / t) = Roasted lime (kg / t) x 0.22 Aggregate slag (kg / t) = Roasted lime (kg / t) x 0.39 Fluorite (kg / t) = In addition to the above, the present invention described above can be applied to ordinary hot metal that has not been subjected to hot metal pretreatment, so that the case of blowing hot metal after pretreatment is particularly advantageous . 2 of the present invention.

【0020】[0020]

【実施例】(実施例1) 図1に示した本発明に係る副原料の投入方法を、溶銑予
備処理後の所謂脱燐溶銑の吹錬に適用し、極低炭素鋼を
溶製した。使用した転炉1は、通称LD−KGCと呼ば
れ、MgO系耐火物2を内張りした、酸素を上吹き、不
活性ガスを底吹きする機能(ノズル又はランス)3、4
を備えたものである(図6参照)。この操業は、スラグ
残し後のチャージとして行われた。なお、使用した溶銑
量は200トンであり、上吹き酸素流量は450Nm3
/min、底吹きアルゴン・ガス流量は4Nm3 /mi
n、吹錬中の溶銑温度は1250〜1650℃であっ
た。なお、表2に示すように、通常溶銑を使用するた
め、実施例2では副原料投入量を増加させ、脱燐を他の
例と同じレベルに維持した。 (実施例2) 実施例1と同じ転炉で、予備処理を施さなかった通常の
溶銑を、スラグ残し後のチャージとして吹錬した。実施
例1と同じ転炉で、同一の脱燐溶銑を、全量排滓した後
のチャージで吹錬した。 (従来例) 実施例1と同じ転炉で、従来の副原料投入法に従い、複
数チャージの吹錬を行った。
Example 1 The method of introducing the auxiliary raw material according to the present invention shown in FIG. 1 was applied to the so-called dephosphorized hot metal after the hot metal pretreatment to blow it, and an extremely low carbon steel was melted. The converter 1 used is commonly referred to as LD-KGC and has a function (nozzle or lance) 3 lined with MgO refractory 2 to blow oxygen upward and blow inert gas bottom.
(See FIG. 6). This operation was performed as a charge after leaving the slag. The amount of hot metal used was 200 tons, and the flow rate of top-blown oxygen was 450 Nm 3.
/ Min, bottom blown argon gas flow rate is 4 Nm 3 / mi
n, the hot metal temperature during blowing was 1250 to 1650 ° C. As shown in Table 2, hot metal is usually used.
For this reason, in Example 2, the amount of auxiliary raw material input was increased and other phosphorus was removed.
Maintained at the same level as the example. (Example 2) In the same converter as in Example 1, ordinary hot metal not subjected to pretreatment was blown as a charge after leaving slag. In the same converter as in Example 1, the same dephosphorized hot metal was blown by the charge after the entire amount was discharged. (Conventional Example) In the same converter as in Example 1, blowing of a plurality of charges was performed according to a conventional auxiliary raw material charging method.

【0021】なお、上記の操業条件及び操業結果を、表
2及び表3に一括して示す。また、使用した溶銑の化学
組成は表4の通りである。
The above operating conditions and operating results are collectively shown in Tables 2 and 3. Table 4 shows the chemical composition of the hot metal used.

【0022】[0022]

【表2】 [Table 2]

【0023】[0023]

【表3】 [Table 3]

【0024】[0024]

【表4】 [Table 4]

【0025】表3より、以下のことが明らかになり、本
発明の有効なことが確認された。表3によれば、本発明
より副原料削減と滓化率歩留向上がみられ、また、スラ
グ残無しの場合でも滓化率は向上している。さらに、通
常溶銑の使用においても、表3に示すように、滓化率向
上の問題はなく、実施可能であった。なお、上記実施例
は、本発明をLD−KGC型転炉に適用したものである
が、本発明は、その他型式の転炉においても適用できる
ことは言うまでもない。
From Table 3, the following facts were clarified, and the effectiveness of the present invention was confirmed. According to Table 3, reduction of secondary raw materials and improvement of the slag formation yield are observed as compared with the present invention, and the slag formation ratio is improved even when there is no slag residue. In addition,
Even when using normal hot metal, as shown in Table 3, the rate of slag formation
There was no problem above and it was feasible. In addition, although the present invention is applied to the LD-KGC type converter in the above-mentioned embodiment, it goes without saying that the present invention can be applied to other types of converters.

【0026】[0026]

【発明の効果】以上述べたように、本発明により、転炉
吹錬の初期から迅速滓化が円滑に行なえるようになる。
その結果、転炉耐火物の溶損防止、スピッティングとダ
ストの発生抑制による溶銑歩留の向上ばかりでなく、使
用する副原料量や合金鉄量の削減も可能となった。
As described above, according to the present invention, rapid slag formation can be smoothly performed from the initial stage of converter blowing.
As a result, not only was it possible to improve the hot metal yield by preventing melting damage of converter refractories and suppressing the generation of spitting and dust, but it was also possible to reduce the amount of auxiliary raw materials and the amount of ferroalloy used.

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

【図1】本発明に係る副原料投入方法の一例を示すパタ
ーン図である。
FIG. 1 is a pattern diagram showing an example of an auxiliary raw material charging method according to the present invention.

【図2】従来の副原料投入方法を示すパターン図であ
る。
FIG. 2 is a pattern diagram showing a conventional auxiliary raw material charging method.

【図3】脱燐溶銑を吹錬中のCaO溶解度の推移を示す
図である。
FIG. 3 is a diagram showing a transition of CaO solubility during dephosphorization hot metal blowing.

【図4】吹止時に溶解しているCaO量を基準にした各
吹錬時期でのCaO溶解度を示す図である。
FIG. 4 is a diagram showing the CaO solubility at each blowing time, based on the amount of CaO dissolved at the time of blowing stop.

【図5】スラグ残し後のチャージと全量排滓後のチャー
ジでのCaO溶解度の比較を示す図である。
FIG. 5 is a diagram showing a comparison of CaO solubility between the charge after leaving the slag and the charge after discharging the whole amount.

【図6】所謂LD−KGC型転炉を示す図である。FIG. 6 is a diagram showing a so-called LD-KGC type converter.

フロントページの続き (56)参考文献 特開 平8−325623(JP,A) 特開 平7−173516(JP,A) 特開 平8−3616(JP,A) 特開 平7−179921(JP,A) 特開 昭55−107715(JP,A) (58)調査した分野(Int.Cl.7,DB名) C21C 1/00 - 7/10 Continuation of the front page (56) Reference JP-A-8-325623 (JP, A) JP-A-7-173516 (JP, A) JP-A-8-3616 (JP, A) JP-A-7-179921 (JP , A) JP-A-55-107715 (JP, A) (58) Fields investigated (Int.Cl. 7 , DB name) C21C 1/00-7/10

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 転炉内の溶銑に、焼石灰、軽焼ドロマイ
ト、生ドロマイト、蛇紋岩、造塊滓及び蛍石を投入して
滓化し、生じたスラグと溶銑間のスラグ−メタル反応を
酸素吹錬下で行わせるに際し、 全吹錬時間の20%から60%の期間内に焼石灰を投入
し、且つその期間内で全投入焼石灰量を複数回に均等分
割して投入すると共に、前記蛇紋岩は、上記焼石灰の投
入期間内で複数回に分割して投入し、前記蛍石は、全吹
錬期間の当初から30%までに投入し、前記軽焼ドロマ
イト及び前記造塊滓は、全吹錬期間の当初から10%ま
でに投入し、前記生ドロマイトは、全吹錬期間の25%
から30%までに投入することを特徴とする転炉への副
原料投入方法。
1. A slag-metal reaction between the generated slag and the hot metal is performed by adding burned lime, light burned dolomite, raw dolomite, serpentine, slag and fluorite to the hot metal in the converter. upon causing under oxygen blowing, along with the full blowing the burnt lime was charged to 20% of the time to 60% of the time, and to introduce and evenly divided into a plurality of times all turned sintered lime amount within that period , The serpentine is the above-mentioned
It is divided into several times during the entry period and put in.
Add up to 30% from the beginning of the smelting period, and light burn doloma
Ito and the agglomerate of slag are 10% from the beginning of the whole blowing period.
The raw dolomite is 25% of the total blowing period.
To 30% from 30 to 30% .
【請求項2】 上記銑鉄を、予備処理後の溶銑とするこ2. The pig iron is used as hot metal after pretreatment.
とを特徴とする請求項1記載の転炉への副原料投入方The method of charging the auxiliary raw material to the converter according to claim 1, wherein
法。Law.
JP15496897A 1997-06-12 1997-06-12 How to add auxiliary raw materials to the converter Expired - Fee Related JP3440755B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15496897A JP3440755B2 (en) 1997-06-12 1997-06-12 How to add auxiliary raw materials to the converter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15496897A JP3440755B2 (en) 1997-06-12 1997-06-12 How to add auxiliary raw materials to the converter

Publications (2)

Publication Number Publication Date
JPH116006A JPH116006A (en) 1999-01-12
JP3440755B2 true JP3440755B2 (en) 2003-08-25

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Country Link
JP (1) JP3440755B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002294322A (en) * 2001-03-28 2002-10-09 Nisshin Steel Co Ltd Slag-making method for converter
JP5929632B2 (en) * 2012-08-27 2016-06-08 新日鐵住金株式会社 Converter refining method
KR101481603B1 (en) * 2012-12-24 2015-01-13 주식회사 포스코 Stainless steel and method of manufacturing the same
CN103555879B (en) * 2013-10-21 2015-01-21 莱芜钢铁集团有限公司 Control method for reducing total iron content of SPHC (steel plate heat commercial) final slag

Also Published As

Publication number Publication date
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