JPH0353014A - Smelting method for extremely low-sulfur steel - Google Patents
Smelting method for extremely low-sulfur steelInfo
- Publication number
- JPH0353014A JPH0353014A JP18495989A JP18495989A JPH0353014A JP H0353014 A JPH0353014 A JP H0353014A JP 18495989 A JP18495989 A JP 18495989A JP 18495989 A JP18495989 A JP 18495989A JP H0353014 A JPH0353014 A JP H0353014A
- Authority
- JP
- Japan
- Prior art keywords
- molten iron
- oxygen
- blowing
- desulfurization
- slag
- 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
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- Carbon Steel Or Casting Steel Manufacturing (AREA)
Abstract
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、転炉における極低硫鋼の溶製に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to the melting of ultra-low sulfur steel in a converter.
一般に、鋼中に硫黄を不純物として含有していると、鋼
と硫化鉄との共晶作用による脆性の低下、或いは炭化物
の球状化阻害による溶接性の悪化等を招く。Generally, when sulfur is contained as an impurity in steel, it causes a decrease in brittleness due to the eutectic interaction between the steel and iron sulfide, or a deterioration in weldability due to inhibition of spheroidization of carbides.
この理由から、旧来より、鋼中の硫黄を低減するために
、例えば特開昭52−19109号公報に示すように、
混銑車内にランスを浸漬して脱硫剤をキャリアーガスと
ともに吹き込む方法か、或いは特開昭56−9308号
公報に示すように、混銑車内にランスを浸漬してキャリ
アガスと共に、ソーダ灰,ホタル石や他の脱硫,脱燐剤
を吹き込んで、同時に脱硫,脱燐を行う等種々の方法が
提案され、その一部は実用化され、かなりの効果を上げ
ている。For this reason, in order to reduce sulfur in steel, for example, as shown in Japanese Patent Application Laid-Open No. 52-19109,
There is a method in which a lance is immersed in a pig iron mixer car and a desulfurizing agent is blown in together with a carrier gas, or as shown in JP-A-56-9308, a lance is immersed in a pig iron mixer car and a desulfurizing agent is blown in with a carrier gas, such as soda ash, fluorite, etc. Various methods have been proposed, such as injecting other desulfurization and dephosphorization agents to perform desulfurization and dephosphorization at the same time, some of which have been put into practical use and have achieved considerable results.
しかしながら、混銑車内にランスを浸漬して脱硫剤、或
いは脱燐,脱硫剤を吹き込んで脱硫か、又は脱硫と脱燐
を同時に行う方法では以下の問題点がある。However, there are the following problems with methods in which a lance is immersed in a pig iron mixer and a desulfurization agent or a desulfurization agent is blown in, or a method in which desulfurization and dephosphorization are performed simultaneously.
まず、かなりの高効率で脱硫,脱燐を行うことができる
が、極低硫,低燐の溶銑を得るには、処理剤の多量使用
及び処理時間の延長と、これに伴う溶銑温度の低下とな
る。First, desulfurization and dephosphorization can be carried out with fairly high efficiency, but in order to obtain extremely low sulfur and low phosphorus hot metal, it is necessary to use a large amount of treatment agent, extend the treatment time, and lower the hot metal temperature accordingly. becomes.
この溶銑温度の低下は転炉操業の阻害となる。This drop in hot metal temperature hinders converter operation.
さらに一般に、溶銑段階の脱硫は、脱硫から転炉装入ま
で時間を要し、その間に復硫を招く。また、前述の予備
処理で極低硫,低燐銑を溶製し、これを転炉に装入して
冷鉄源,副原料等を添加して吹錬しても、これ等の装入
物、或いは前吹錬の残存スラグ、又は炉体内張り耐火物
やコーティング材等から逆に溶鋼中の硫黄分が上昇する
、いわゆる復硫現象を生じる。Furthermore, desulfurization at the hot metal stage generally requires time from desulfurization to charging into a converter, and during that time, resulfurization occurs. In addition, even if extremely low sulfur and low phosphorus pig iron is smelted in the preliminary treatment described above, charged into a converter, and blown with the addition of a cold iron source and auxiliary materials, etc. The so-called resulfurization phenomenon occurs in which the sulfur content in the molten steel increases from the slag remaining from pre-blowing, the refractory lining inside the furnace, coating materials, etc.
これ等の理由から、本発明は、同一の転炉において脱硫
と脱燐を各工程毎に行い、復硫を防止するとともに、転
炉内の脱硫反応を促進せしめて、従来不可能であったレ
ベルの極低硫鋼の溶製を可能にするとともに、従来法に
比べて耐火物,脱硫剤コストの低減をも図ることのでき
る極低硫鋼の溶製法を提供することにある。For these reasons, the present invention performs desulfurization and dephosphorization in each process in the same converter, prevents resulfurization, and promotes the desulfurization reaction in the converter, which was previously impossible. It is an object of the present invention to provide a method for producing ultra-low sulfur steel, which enables the production of ultra-low sulfur steel of the same level as the conventional method, and also reduces the cost of refractories and desulfurization agents compared to conventional methods.
本発明は、転炉で極低硫鋼を溶製するに際して、転炉吹
諌を第1段階として溶鉄中のCが0.3〜2.5%にな
るまで脱珪脱炭吹錬し、この後、該溶鉄に脱硫剤を添加
して脱硫処理を行うとともに、脱硫処理後のスラグを炉
内から排滓し、次いで第2段階として脱燐剤を添加して
吹酸することにある。When melting ultra-low sulfur steel in a converter, the present invention uses converter blowing as the first step, and performs desiliconization and decarburization blowing until C in the molten iron reaches 0.3 to 2.5%, Thereafter, a desulfurization agent is added to the molten iron to perform a desulfurization treatment, and the slag after the desulfurization treatment is discharged from the furnace.Then, as a second step, a dephosphorization agent is added and acid blowing is carried out.
ここで第l段階の脱珪,脱炭、若しくは脱炭を行う初期
吹酸において溶鉄中のCが0.・3〜2.5%とする理
由は、Cが2.5%より高いと溶鉄の温度が十分に上昇
せず、溶跣炉外脱硫処理に比べて温度の上昇による脱硫
反応促進の効果が得られない。Here, in the first stage of desiliconization, decarburization, or initial blowing acid for decarburization, C in the molten iron is 0.・The reason for setting it at 3 to 2.5% is that if the C content is higher than 2.5%, the temperature of the molten iron will not rise sufficiently, and the desulfurization reaction will be less effective in accelerating the desulfurization reaction compared to desulfurization treatment outside the melting furnace. I can't get it.
一方、Cを0.3%より低いレベルまで吹錬すると、溶
鉄が酸化され、スラグ中の酸素ポテンシャルが上昇、或
いは鋼中の酸素濃度が上昇し、温度は高いが脱硫には不
利なスラグ組成と溶鉄組織となってしまう。従って、こ
のレベルで脱硫しようとすると大量の脱酸剤(AJ.A
j!ドロス等)が必要で、生石灰の原単位も上昇してし
まう。On the other hand, when C is blown to a level lower than 0.3%, the molten iron is oxidized, the oxygen potential in the slag increases, or the oxygen concentration in the steel increases, resulting in a slag composition that is disadvantageous for desulfurization although the temperature is high. This results in a molten iron structure. Therefore, if you try to desulfurize at this level, a large amount of deoxidizing agent (AJ.
j! dross, etc.), and the unit consumption of quicklime also increases.
つまり、溶鉄中のCを0.3%以上で吹酸停止すると、
溶鉄中及びスラグ中の酸素濃度を上昇させないため、こ
の状態における脱硫効率は極めて高い。この脱硫は、不
活性ガスをキャリアーガスとして上吹ランスから吹き付
けるか、或いは浸漬せしめて吹き込みと攪拌を行っても
良い。また、底吹羽口から上記脱硫剤をキャリアーガス
とともに吹き込んでも良い。In other words, when C in molten iron is stopped blowing with acid at 0.3% or more,
Since the oxygen concentration in the molten iron and slag does not increase, the desulfurization efficiency in this state is extremely high. This desulfurization may be carried out by blowing an inert gas as a carrier gas from a top blowing lance, or by immersing it in the air and performing blowing and stirring. Alternatively, the desulfurizing agent may be blown in together with the carrier gas from the bottom blowing tuyere.
脱硫剤としては、生石灰,ホタル石.金属Af,アルミ
ドロス等の一種以上からなるものを用いる。Quicklime and fluorspar are used as desulfurizing agents. A material made of one or more of metal Af, aluminum dross, etc. is used.
転炉でかかる処理を行うことにより、炉外の一般脱硫に
比べて、大量のガス吹き込みによる強撹拌の実現による
反応促進と、溶鉄の脱炭発熱による溶鉄温度300℃程
度上昇でき、しかも溶鉄及びスラグ中の酸素濃度を抑制
できる等から、好ましい高効率脱硫が可能となる。By performing such treatment in a converter, compared to general desulfurization outside the furnace, the reaction can be accelerated by strong stirring achieved by blowing a large amount of gas, and the molten iron temperature can be raised by about 300°C due to the heat generated by decarburization of the molten iron. Since the oxygen concentration in the slag can be suppressed, desirable high-efficiency desulfurization is possible.
また、溶鉄及びスラグ中の酸素を脱酸するための還元剤
であるAf,或いはアルミドロスの使用量も節減できる
。このように脱硫処理後は、生戊スラグを傾動排滓、或
いは機械的な掻き出し、真空吸引等のいずれかによって
除去する。これは第2段階の脱燐と仕上脱炭の際に供給
する酸素によって脱炭が進行し、Cが低くなると鉄が酸
化されスラグ中に入り、脱硫反応CaO+S→CaS+
○の平衡がずれて逆反応が進行し、復硫がおこるため、
脱硫滓は排滓しておく。Furthermore, the amount of Af or aluminum dross used as a reducing agent for deoxidizing oxygen in molten iron and slag can be reduced. After the desulfurization treatment, the raw slag is removed by tilting slag, mechanical scraping, vacuum suction, or the like. This is because decarburization progresses due to the oxygen supplied during the second stage of dephosphorization and final decarburization, and when the C content becomes low, iron is oxidized and enters the slag, resulting in the desulfurization reaction CaO+S→CaS+
The equilibrium of ○ is shifted and the reverse reaction progresses, causing resulfurization.
Drain the desulfurization slag.
次に第2&階において炉内に生石灰,ホタル石.ドロマ
イト,鉄鉱石等の一種若しくは二種以上からなる脱燐剤
を添加して吹酸する。この吹酸によって脱燐と仕上脱炭
を行い、所定の戊分となった溶鋼を得る。ここで適用で
きる転炉としては、上吹き、或いは上底吹きのいずれで
も良い。Next, on the second floor, quicklime and fluorite were placed in the furnace. A dephosphorizing agent consisting of one or more of dolomite, iron ore, etc. is added and acid blown. This blown acid performs dephosphorization and final decarburization to obtain molten steel with a predetermined fraction. The converter that can be applied here may be either a top blowing type or a top and bottom blowing type.
このように転炉での吹諌において脱硫処理を転炉内で行
い、排滓後に脱燐処理を組み合わせることで戊品Sが5
QPPM以下の高純度鋼の溶製が可能となり、同時に低
燐の高純度鋼の溶製を実現し、しかも総合的な処理コス
トを低減できる。In this way, by performing the desulfurization treatment in the converter during the slag discharge, and combining it with the dephosphorization treatment after the slag is discharged, it is possible to increase the
It is possible to produce high-purity steel of QPPM or less, and at the same time, it is possible to produce high-purity steel with low phosphorus, and the overall processing cost can be reduced.
第1図に本発明の一例による処理フローを示す。 FIG. 1 shows a processing flow according to an example of the present invention.
図において、混銑車1内で浸漬ランス2からCab,(
:aFz,酸化鉄等を吹き込んで、事前に脱珪処理され
た溶銑を脱硫と脱燐処理を行う。この溶銑を溶銑鍋3に
より上底吹転炉4に装入する。ここで、上吹きランス5
から酸素を吹き込むとともに、炉底羽口6から一部酸素
と冷却ガス(C.H. , C○,等)を吹き込んで通
常の脱珪,脱炭吹諌を行う。In the figure, Cab, (
: AFz, iron oxide, etc. are blown into the hot metal, which has been desiliconized in advance, to be desulfurized and dephosphorized. This hot metal is charged into a top-bottom blowing converter 4 through a hot metal ladle 3. Here, top blow lance 5
Oxygen is blown in from the furnace bottom, and some oxygen and cooling gas (C.H., C○, etc.) are blown in from the bottom tuyere 6 to carry out normal desiliconization and decarburization.
脱珪溶跣については、脱炭を主体に行う。この脱炭吹諌
の後は、上吹ランス5 (或いは羽口6でもよい)から
脱硫剤を吹き込むか、或いは該ランス5を浴中に浸漬し
て脱硫剤を吹き込んでも良い。Regarding desiliconization, decarburization is mainly carried out. After this decarburization, the desulfurizing agent may be blown from the top blowing lance 5 (or the tuyere 6), or the lance 5 may be immersed in the bath and the desulfurizing agent may be blown into the bath.
また、羽口6からはN2,^r , C O 2等の羽
口保謹のための少量ガスを流すか、或いは、むしろ増量
して浴内撹拌を強化することも好ましい。この脱硫剤と
しては、生石灰,ホタル石,アルミドロス,金属アルミ
等の一種若しくは二種以上を組み合わせて吹き込む。こ
の代表組戒と原単位を表−1に示す。Further, it is also preferable to flow a small amount of gas such as N2, ^r, CO2, etc. for tuyere protection from the tuyere 6, or rather to increase the amount to strengthen the stirring in the bath. As the desulfurizing agent, one or a combination of two or more of quicklime, fluorite, aluminum dross, metallic aluminum, etc., is injected. The representative group precepts and basic units are shown in Table 1.
表−1
前述の如くして、約15〜20分の脱硫処理によって、
20〜50PPMの強脱硫が行われる。この脱硫終了後
は、転炉4を傾転してスラグ7を掻き出して排出する。Table 1 As mentioned above, by desulfurization treatment for about 15 to 20 minutes,
Strong desulfurization of 20 to 50 PPM is performed. After the desulfurization is completed, the converter 4 is tilted to scrape out the slag 7 and discharge it.
さらに、炉内に脱燐剤である生石灰.ドロマイト,ホタ
ル石等を添加して、上吹ランス5から酸素と羽口6から
一部の酸素と羽口6の冷却ガス(C.}l.. C○
,〉を吹き込んで脱燐と脱炭の仕上を行う。Furthermore, quicklime, a dephosphorizing agent, is placed inside the furnace. Dolomite, fluorite, etc. are added, and oxygen from the top blowing lance 5, some oxygen from the tuyere 6, and cooling gas (C.}l..C○
,〉 is blown in to complete dephosphorization and decarburization.
この工程別精錬によって極低硫化の実現はもちろん低燐
化をも達成でき、従来不可能か或いは二次精錬負荷増を
招いていた高純度鋼が容易に得られる。Through this step-by-step refining, not only extremely low sulfurization but also low phosphorus can be achieved, and high-purity steel can be easily obtained, which was previously impossible or required an increase in the load of secondary refining.
従来還元反応である脱硫は、転炉の酸化精錬炉内では、
大量の生石灰使用で30〜50%の脱硫しか望めず、極
低硫鋼では、逆に復硫を生じて鋼中硫黄の上昇となる。Desulfurization, which is a conventional reduction reaction, is carried out in the oxidation smelting furnace of a converter.
If a large amount of quicklime is used, only 30 to 50% desulfurization can be expected, and in extremely low sulfur steel, resulfurization occurs and the sulfur content in the steel increases.
しかし、転炉内で吹酸脱炭後の高温溶鉄中に脱硫剤を添
加した精錬は、溶鉄の高温度と強撹拌及び還元雰囲気の
保持による脱硫となり、脱硫反応の大幅な向上が達或さ
れ、しかも脱硫剤及び還元剤の消費が少なくてすむ。ま
た、この処理によって従来では不可能な極低燐.低硫の
高純度鋼の溶製が可能となった。However, in refining in which a desulfurizing agent is added to high-temperature molten iron after decarburizing blown acid in a converter, desulfurization occurs due to the high temperature of the molten iron, strong stirring, and maintaining a reducing atmosphere, and a significant improvement in the desulfurization reaction has not been achieved. Moreover, the consumption of desulfurizing agent and reducing agent can be reduced. This treatment also allows for ultra-low phosphorus, which is impossible with conventional methods. It has become possible to produce high-purity steel with low sulfur content.
次に、本発明による高純度鋼を175t転炉で同一の溶
銑を用いた従来溶製法と比較した結果を表−2に示す。Next, Table 2 shows the results of comparing the high-purity steel of the present invention with the conventional melting method using the same hot metal in a 175-ton converter.
本法は脱硫剤原単位が約半分にもかかわらず、(S)/
(S)を大幅に向上できるため、到達(S)も20P
PMまで低減し高純度化を図ることができた。Although this method uses about half the desulfurization agent consumption, (S)/
(S) can be greatly improved, so reaching (S) is also 20P
It was possible to achieve high purity by reducing even PM.
これに対して、通常の転炉内脱炭精錬を行った従来法で
は、脱硫剤原単位も高く、しかも到達〔S〕が高く、高
純度鋼の溶製が困難である。On the other hand, in the conventional method of decarburization refining in a normal converter, the unit consumption of the desulfurizing agent is high, and the attainment [S] is also high, making it difficult to melt and produce high-purity steel.
表−2 脱燐銑を用いた結果である。Table-2 This is the result using dephosphorized pig iron.
注)いずれも炉外脱硫,
〔発明の効果〕
以上述べた如く、本発明の極低硫閤の溶製方法を用いる
ことにより、従来炉内復硫によって溶製不可能であった
極低硫鋼の製造を可能にするとともに、低硫,低燐の高
純度鋼が溶製できる。また、精錬を短時間で行い得るこ
とから、使用する諸原単位の大幅な節減と、二次精錬処
理等の省略によるコスト低減や、転炉での洗い材の確保
が不要となり、
生産計画立案等が極めて容易になる等の優れた効果が期
待できる。Note) Both are desulfurization outside the furnace. [Effects of the invention] As stated above, by using the method for producing ultra-low sulfur sulfur of the present invention, extremely low sulfur can be produced, which was conventionally impossible to produce by in-furnace resulfurization. In addition to making it possible to manufacture steel, it also enables the production of high-purity steel with low sulfur and low phosphorus. In addition, since smelting can be carried out in a short time, it is possible to significantly reduce the unit consumption, reduce costs by omitting secondary smelting processes, and eliminate the need to secure washing materials for the converter, making production planning easier. Excellent effects such as making it extremely easy to do the following can be expected.
第l図は本発明による処理フローの一例を示す。 FIG. 1 shows an example of a processing flow according to the present invention.
Claims (1)
、この溶鉄中のCが0.3〜2.5%で酸素の供給を停
止するとともに、溶鉄に脱硫剤を添加して脱硫処理して
後に、該脱硫スラグを排滓し、次いで脱燐用造滓剤を添
加して吹酸することを特徴とした極低硫鋼の溶製方法。1. Oxygen blowing is performed by adding molten iron, cold iron material, and slag-forming agent, and when the C content in the molten iron is 0.3 to 2.5%, the supply of oxygen is stopped, and a desulfurization agent is added to the molten iron. 1. A method for producing ultra-low sulfur steel, which comprises performing a desulfurization treatment on the steel, then draining the desulfurization slag, and then adding a dephosphorization slag forming agent and blowing acid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18495989A JPH0353014A (en) | 1989-07-17 | 1989-07-17 | Smelting method for extremely low-sulfur steel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18495989A JPH0353014A (en) | 1989-07-17 | 1989-07-17 | Smelting method for extremely low-sulfur steel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0353014A true JPH0353014A (en) | 1991-03-07 |
Family
ID=16162343
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18495989A Pending JPH0353014A (en) | 1989-07-17 | 1989-07-17 | Smelting method for extremely low-sulfur steel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0353014A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6608594B1 (en) | 1999-10-08 | 2003-08-19 | Matsushita Electric Industrial Co., Ltd. | Antenna apparatus and communication system |
| US6639555B1 (en) | 1998-07-02 | 2003-10-28 | Matsushita Electric Industrial Co., Ltd. | Antenna unit, communication system and digital television receiver |
| CN112695147A (en) * | 2020-12-18 | 2021-04-23 | 芜湖新兴铸管有限责任公司 | Low-oxygen steel tapping production method for bearing steel converter |
-
1989
- 1989-07-17 JP JP18495989A patent/JPH0353014A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6639555B1 (en) | 1998-07-02 | 2003-10-28 | Matsushita Electric Industrial Co., Ltd. | Antenna unit, communication system and digital television receiver |
| US6608594B1 (en) | 1999-10-08 | 2003-08-19 | Matsushita Electric Industrial Co., Ltd. | Antenna apparatus and communication system |
| CN112695147A (en) * | 2020-12-18 | 2021-04-23 | 芜湖新兴铸管有限责任公司 | Low-oxygen steel tapping production method for bearing steel converter |
| CN112695147B (en) * | 2020-12-18 | 2022-03-01 | 芜湖新兴铸管有限责任公司 | Low-oxygen steel tapping production method for bearing steel converter |
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