JPS6235445B2 - - Google Patents

Info

Publication number
JPS6235445B2
JPS6235445B2 JP58116493A JP11649383A JPS6235445B2 JP S6235445 B2 JPS6235445 B2 JP S6235445B2 JP 58116493 A JP58116493 A JP 58116493A JP 11649383 A JP11649383 A JP 11649383A JP S6235445 B2 JPS6235445 B2 JP S6235445B2
Authority
JP
Japan
Prior art keywords
slag
converter
hot metal
blowing
steel
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
Application number
JP58116493A
Other languages
Japanese (ja)
Other versions
JPS609813A (en
Inventor
Teruyoshi Hiraoka
Yoshuki Kasuya
Kaoru Ichikawa
Hiroaki Yamamoto
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 JP11649383A priority Critical patent/JPS609813A/en
Publication of JPS609813A publication Critical patent/JPS609813A/en
Publication of JPS6235445B2 publication Critical patent/JPS6235445B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C5/00Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
    • C21C5/28Manufacture of steel in the converter
    • C21C5/30Regulating or controlling the blowing
    • C21C5/32Blowing from above

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、溶銑予備処理によつて成品レベルま
で脱Pした溶銑を用い且つ転炉スラグを炭素含有
物質で還元して復マンガンを図ることにより吹止
〔Mn〕を上昇させ、かつ鋼中酸素レベルを低下さ
せる方法に関するものである。 転炉製鋼法においては、その酸素供給形態によ
つて上吹き、上底吹き、底吹等があるが、その反
応機構の基本は同等であるため、以下上吹き転炉
について述べる。純酸素上吹き転炉製鋼法は、転
炉上部からランスを通して純酸素を銑鉄上に吹き
込み、そのジエツトの衝突による撹拌力によつて
反応を促進させ、銑鉄中の不純物を酸化し、それ
ら酸化物を銑鉄上に存在するスラグに吸収させ除
去することによつて銑鉄から鋼を作る方法であ
る。 転炉吹錬開始にあたつては、スラグの主成分で
あるCaO系の副原料を転炉内に投入し、酸素の吹
き込みを行なう。 吹錬の進行に伴い、まず銑鉄中のシリコンが優
先的に酸化され(SiO2)となる。この(SiO2)が
固体の状態のCaOを溶解し、他の不純物を吸収し
うる活性化したスラグを生成する。この時期には
〔Mn〕、〔P〕の酸化も進行し、それぞれ
(MnO)、(P2O5)の形となつて活性化したスラグ
に吸収されていく。〔Si〕が優先酸化される時期
(いわゆる“Si吹き”)が終わると、次に〔C〕の
酸化が始まり、吹き込まれる酸素のほぼ全量が銑
鉄中の〔C〕と反応する時期(脱炭最盛期)を迎
える。 この時期には〔Mn〕、〔P〕等の酸化に寄与す
る(FeO)の生成がにぶるため銑鉄及びスラグ中
の〔Mn〕、〔P〕の変化が止まる。 脱炭最盛期の末期になると造滓がかなり進行
し、均一な溶融スラグが形成されるようになる
と、スラグ中の(MnO)や(FeO)が還元され
て溶鋼中にもどつてくる〔Mn〕隆起の現象が見
られる。 この脱炭速度がおちる時期以降再びFeOの増加
に伴う〔Mn〕、〔P〕の酸化が盛んに行なわれ、
〔C〕、〔Mn〕、〔P〕の低い鋼の生成に到る。従つ
て転炉精錬においては、不純物除去の観点から適
正なスラグを作ることが大きなポイントとなる。 低燐鋼(成品〔P〕0.02%、ことに0.015
%)を溶製する場合、従来は燐酸化物(P2O5)の
吸収除去するCaO系副原料を多量に投入し、又場
合によつては吹錬途中に排滓し、それまでに吸収
した(P2O5)を炉外に排出し、新ためてCaO系副
原料を投入し、再び吹錬を行なう(いわゆるダブ
ル・スラグ法)等の方法がとられている。しかし
ながらこれらの方法では到達燐に限界があり、又
酸化反応を強力に促進するため〔P〕のみなら
ず、〔Mn〕を増加するために添加した鉄Mn鉱石
中の〔Mn〕も酸化除去されてしまい、出鋼以降
のMn合金鉄添加量が増大し、従つて従来法では
〔P〕が低く〔Mn〕の高い鋼を得る場合、コスト
高となつていた。しかも鋼中の酸素レベルが高い
ために、投入合金鉄による脱酸生成物が増大し、
介在物の増加を来たしていた。 本発明は、上記の欠点を除去するためになされ
たもので、次の2つの構成を要件とするものであ
る。 先づ第1は、転炉に装入する溶銑を予備処理し
て成品レベルまで脱Pした溶銑を炉内に装入する
ことであり、その第2は、転炉精錬末期の脱炭反
応減衰期にスラグを積極的に還元して復Mnを図
ることである。 本発明者等は、吹錬末期の酸化反応形態に着目
し、スラグ中の(MnO)を還元し、復マンガン
を計る目的で、この時期に炭素含有物質をスラグ
に対して添加した。その結果、酸素との親和力の
弱い燐の方が優先的に還元され、復マンガンは僅
小であり、いわゆる低燐高Mn鋼の溶製上好まし
くないことを確認した。 そこで本発明では、スラグミニマム状態で脱炭
のみ行ない、吹止〔Mn〕を高める為に鉄マンガ
ン鉱石を添加する吹錬において、成品レベルまで
脱燐した溶銑を用いることにより、Pの還元を抑
え、鉄マンガン鉱石(酸化Mn)の還元率を効率
的に上昇せしめて吹止〔Mn〕を一層高め、同時
にスラグ還元により鋼中酸素レベルを低下できる
ものである。溶銑の事前処理により脱Pする方法
は既に公知であるが、その一例を示せば、例えば
脱Si後の溶銑浴に気酸、焼結鉱、CaO、CaF2
を添加し撹拌することにより容易に脱Pすること
ができる。 以下に本発明の内容を図面に基づき更に詳細に
説明する。 第1図ア,イ及びウに、溶銑予備処理により脱
燐(〔P〕=0.015%)した溶銑を用いた純酸素上
吹転炉吹錬中の溶鉄中及びスラグ中の成分挙動の
一例を示す。第1図アに示す如く、脱炭最盛期を
過ぎ、脱炭酸素効率が低下しはじめる点(CB
点)以降にはイに示す如くスラグ中の(FeO)が
急激に増加し、それまでにぶつていた〔Mn〕、
〔P〕の酸化が再びおこり、ウに示す如く、それ
までに鉄マンガン鉱石投入により上昇した溶鉄中
の〔Mn〕が低下し、スラグに移行する。この時
期に本発明方法に従つて、スラグ上方から炭素含
有物質例えば塊状コークスをスラグ中に添加する
とこの酸化物が還元され、〔Mn〕が鋼中に戻る。
この場合P含有量の高い通常の溶銑を用いれば、
スラグ中の(P2O5)も高くなり、これが優先的に
還元され、(MnO)の還元が僅少となるが、低P
銑を用いることによりスラグ中の(MnO)の還
元が十分に行なえるものである。 炭素含有物質を吹錬の初期及び中期に添加して
転炉発生ガスの増加を計ることは公知の技術であ
るが、本発明は上記時期では効果が僅少であり、
脱炭最盛期を過ぎた(CB点以降)吹錬末期で行
なう。 炭素含有物質としてはコークス、石炭ピツチ、
グラフアイト、木炭等が選ばれる該炭素源を添加
する方法として副原料口等から投入する場合、転
炉の排ガス吸収と落下による溶鉄中への溶解等の
阻害要因があるため、スラグ層への歩留りの観点
から、その粒径は5m/mから30m/m程度が好ま
しい。投入方法としては副原料口からの上方添加
あるいはスラグへの直接インジエクシヨン等が考
えられる。 実施例 100t転炉において、第1表に示すごとき成分の
溶銑を脱Si後脱P及び脱S処理して得た第2表の
低P溶銑を用い、第3表に示すごとき副原料を使
用して吹錬を行なつた。 その結果第4表に示すごとき吹止め時の成分を
得た。 本発明によつて従来法に比べ約0.1%マンガン
の高い低燐鋼を転炉において溶製することができ
た。 (1) 高炉溶銑成分
The present invention uses hot metal that has been dephosphorized to a finished product level through hot metal pretreatment, and reduces converter slag with a carbon-containing substance to recover manganese, thereby increasing the blowout [Mn] and reducing the oxygen content in the steel. It concerns how to reduce the level. In the converter steel manufacturing process, there are top blowing, top blowing, bottom blowing, etc. depending on the oxygen supply form, but since the basic reaction mechanism is the same, the top blowing converter will be described below. In the pure oxygen top-blown converter steelmaking method, pure oxygen is blown onto the pig iron through a lance from the top of the converter, and the reaction is accelerated by the stirring force generated by the collision of the jets, oxidizing impurities in the pig iron and removing these oxides. This is a method of making steel from pig iron by absorbing and removing slag present on the pig iron. When starting converter blowing, CaO-based auxiliary materials, which are the main component of slag, are introduced into the converter and oxygen is blown into the converter. As blowing progresses, silicon in the pig iron is preferentially oxidized to (SiO 2 ). This (SiO 2 ) dissolves the solid state CaO and produces an activated slag that can absorb other impurities. During this period, oxidation of [Mn] and [P] also progresses, and they become (MnO) and (P 2 O 5 ), respectively, and are absorbed into the activated slag. After the period in which [Si] is preferentially oxidized (so-called "Si blowing"), the oxidation of [C] begins, and the period in which almost all of the blown oxygen reacts with [C] in the pig iron (decarburization) reaching its peak). During this period, the production of (FeO), which contributes to the oxidation of [Mn], [P], etc., slows down, so changes in [Mn] and [P] in the pig iron and slag stop. At the end of the peak decarburization period, slag formation has progressed considerably and a uniform molten slag is formed. (MnO) and (FeO) in the slag are reduced and return to the molten steel [Mn] A phenomenon of upheaval can be seen. After the time when this decarburization rate slows down, oxidation of [Mn] and [P] occurs again as FeO increases,
This results in the production of steel with low [C], [Mn], and [P]. Therefore, in converter refining, it is important to create an appropriate slag from the viewpoint of removing impurities. Low phosphorus steel (finished product [P] 0.02%, especially 0.015
%), conventionally, a large amount of CaO-based auxiliary raw material, which absorbs and removes phosphorus oxides (P 2 O 5 ), is input, and in some cases, the slag is discharged during blowing, so that the absorption and removal of phosphorus oxides (P 2 O 5 Methods such as discharging the (P 2 O 5 ) from the furnace, introducing new CaO-based auxiliary raw materials, and performing blowing again (so-called double slag method) are used. However, these methods have a limit to the amount of phosphorus that can be reached, and because they strongly promote the oxidation reaction, not only [P] but also [Mn] in the iron-Mn ore added to increase [Mn] is removed by oxidation. As a result, the amount of Mn alloy ferroadded after tapping increases, and therefore, in the conventional method, when obtaining steel with low [P] and high [Mn], the cost becomes high. Moreover, due to the high oxygen level in the steel, deoxidation products from the input ferroalloy increase,
This resulted in an increase in inclusions. The present invention was made to eliminate the above-mentioned drawbacks, and requires the following two configurations. The first step is to pre-treat the hot metal to be charged into the converter and charge the hot metal into the furnace, which has been dephosphorized to the finished product level. The goal is to actively return slag during the period to recover Mn. The present inventors focused on the oxidation reaction form at the final stage of blowing, and added a carbon-containing substance to the slag at this stage for the purpose of reducing (MnO) in the slag and measuring remanganese. As a result, it was confirmed that phosphorus, which has a weaker affinity with oxygen, was preferentially reduced, and the amount of remanganese was very small, which is not preferable for the production of so-called low-phosphorus, high-Mn steel. Therefore, in the present invention, only decarburization is performed in the slag minimum state, and P reduction is suppressed by using hot metal that has been dephosphorized to the finished product level during blowing in which ferromanganese ore is added to increase the blowstop [Mn]. , it is possible to efficiently increase the reduction rate of ferromanganese ore (Mn oxide), further increase the blowout [Mn], and at the same time reduce the oxygen level in the steel through slag reduction. Methods for dephosphorization by pre-treatment of hot metal are already known, but one example is that by adding gas acid, sintered ore, CaO, CaF 2 , etc. to the hot metal bath after deSi removal and stirring. It is possible to de-P. The contents of the present invention will be explained in more detail below based on the drawings. Figure 1 A, B, and C show an example of the behavior of components in molten iron and slag during pure oxygen top-blowing converter blowing using hot metal that has been dephosphorized ([P] = 0.015%) by hot metal pretreatment. show. As shown in Figure 1A, the point at which the decarburization oxygen efficiency begins to decline after the peak decarburization period (C B
After point), (FeO) in the slag increases rapidly as shown in (a), and [Mn], which had hitherto encountered
The oxidation of [P] occurs again, and as shown in c, the [Mn] in the molten iron, which had previously increased due to the addition of ferromanganese ore, decreases and transfers to slag. At this stage, according to the method of the present invention, if a carbon-containing substance, such as lump coke, is added to the slag from above the slag, this oxide is reduced and [Mn] returns to the steel.
In this case, if ordinary hot metal with high P content is used,
(P 2 O 5 ) in the slag also increases, and this is preferentially reduced, and the reduction of (MnO) becomes slight, but with low P
By using pig iron, (MnO) in the slag can be sufficiently reduced. It is a known technique to increase the gas generated in the converter by adding carbon-containing substances at the early and middle stages of blowing, but the present invention has little effect at the above-mentioned stage.
This is done at the end of the blowing stage, after the peak decarburization stage (after point C B ). Carbon-containing substances include coke, coal pitch,
When adding carbon sources such as graphite and charcoal from the auxiliary raw material port, there are inhibiting factors such as absorption of exhaust gas from the converter and dissolution into the molten iron due to falling. From the viewpoint of yield, the particle size is preferably about 5 m/m to 30 m/m. Possible feeding methods include upward addition from the auxiliary raw material port or direct injection into the slag. Example In a 100t converter, low-P hot metal shown in Table 2 obtained by removing Si and then deP and S removal from hot metal having the components shown in Table 1 was used, and auxiliary materials shown in Table 3 were used. and performed blowing. As a result, the components shown in Table 4 at the time of blow-off were obtained. According to the present invention, a low phosphorus steel containing about 0.1% higher manganese than conventional methods could be melted in a converter. (1) Blast furnace hot metal components

【表】 (2) 転炉容量:純酸素上吹転炉 100ton (3) 装入溶銑成分【table】 (2) Converter capacity: Pure oxygen top-blown converter 100ton (3) Composition of charged hot metal

【表】 (4) 装入溶銑温度:1375℃ (5) 副原料使用量【table】 (4) Charging hot metal temperature: 1375℃ (5) Amount of auxiliary raw materials used

【表】 従来法 上記(1)〜(5)の条件で、第2図に示す如き吹錬方
法で実施した。 本発明方法 上記(1)〜(5)の条件で、第3図に示す如き吹錬方
法で実施した。第3図におけるコークス投入量は
7Kg/T-Sである。 上記の如く実施した結果を第4表に示す。
[Table] Conventional method Under the conditions (1) to (5) above, blowing was carried out using the blowing method shown in Figure 2. Method of the Invention The blowing method as shown in FIG. 3 was carried out under the conditions (1) to (5) above. The amount of coke input in Figure 3 is 7Kg/TS. The results of the experiment as described above are shown in Table 4.

【表】【table】 【図面の簡単な説明】[Brief explanation of the drawing]

第1図ア,イ及びウは脱炭酸素効率、スラグ中
及び溶鉄中の成分挙動の一例を示すグラフ、第2
図及び第3図は実施例における従来法及び本発明
方法の吹錬パターンを示す図表である。
Figure 1 A, B and C are graphs showing examples of decarburization oxygen efficiency and component behavior in slag and molten iron.
3 and 3 are charts showing the blowing patterns of the conventional method and the method of the present invention in Examples.

Claims (1)

【特許請求の範囲】[Claims] 1 転炉内へ溶銑及び含Mn物質を装入して造滓
剤使用の下、酸素吹錬を行い吹止Mnの高い鋼を
得るにさいし、上記溶銑として予備処理によつて
成品レベルまで脱Pした低P溶銑を用い、且つ転
炉精錬末期の脱炭反応減衰期に粉、粒又は塊状の
炭素含有物質を上方添加してスラグ層に到達せし
めスラグを還元することにより復Mnを図ること
を特徴とする転炉における吹止Mn上昇精錬方
法。
1 When hot metal and Mn-containing materials are charged into a converter and subjected to oxygen blowing using a slag-forming agent to obtain steel with a high blowout Mn, the hot metal is decomposed to a finished product level through preliminary treatment. To regenerate Mn by using P-polluted low-P hot metal and adding powder, granular, or lumpy carbon-containing substances upward during the decarburization reaction decay period at the end of converter refining to reach the slag layer and reduce the slag. A blow-stop Mn ascending refining method in a converter characterized by the following.
JP11649383A 1983-06-28 1983-06-28 Refining method by increasing blown-out mn in converter Granted JPS609813A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11649383A JPS609813A (en) 1983-06-28 1983-06-28 Refining method by increasing blown-out mn in converter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11649383A JPS609813A (en) 1983-06-28 1983-06-28 Refining method by increasing blown-out mn in converter

Publications (2)

Publication Number Publication Date
JPS609813A JPS609813A (en) 1985-01-18
JPS6235445B2 true JPS6235445B2 (en) 1987-08-01

Family

ID=14688491

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11649383A Granted JPS609813A (en) 1983-06-28 1983-06-28 Refining method by increasing blown-out mn in converter

Country Status (1)

Country Link
JP (1) JPS609813A (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5591914A (en) * 1978-12-28 1980-07-11 Sumitomo Metal Ind Ltd Manufacture of manganese steel
JPS55128519A (en) * 1979-03-24 1980-10-04 Sumitomo Metal Ind Ltd Enhancing of steel tapping yield

Also Published As

Publication number Publication date
JPS609813A (en) 1985-01-18

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