JPH10245617A - Steelmaking method using plural converters - Google Patents

Steelmaking method using plural converters

Info

Publication number
JPH10245617A
JPH10245617A JP6739197A JP6739197A JPH10245617A JP H10245617 A JPH10245617 A JP H10245617A JP 6739197 A JP6739197 A JP 6739197A JP 6739197 A JP6739197 A JP 6739197A JP H10245617 A JPH10245617 A JP H10245617A
Authority
JP
Japan
Prior art keywords
refining
content
hot metal
steel
converter
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
JP6739197A
Other languages
Japanese (ja)
Other versions
JP3486887B2 (en
Inventor
Yoshimi Komatsu
喜美 小松
Haruyoshi Tanabe
治良 田辺
Hirohisa Nakajima
廣久 中島
Satoshi Kodaira
悟史 小平
Ichiro Kikuchi
一郎 菊地
Manabu Arai
学 新井
Hideshige Tanaka
秀栄 田中
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 Engineering Corp
Original Assignee
NKK Corp
Nippon Kokan Ltd
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 NKK Corp, Nippon Kokan Ltd filed Critical NKK Corp
Priority to JP06739197A priority Critical patent/JP3486887B2/en
Publication of JPH10245617A publication Critical patent/JPH10245617A/en
Application granted granted Critical
Publication of JP3486887B2 publication Critical patent/JP3486887B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To improve the productivity of a steel by using molten iron having <=0.3wt.% Si, refining P content of the molten iron to a standard value or lower of crude steel and shortening dephosphorize-refining time as less as possible, in the dephosphorization of molten iron in a converter. SOLUTION: (a) In one side of the converter, the molten iron having <=0.3wt.% silicon(Si) content is dephosphorized within a prescribed time and the phosphorus(P) content in the molten iron is refined to the P content (the component standard value of the steel) or lower needed to the crude steel. (b) The dephosphorized molten iron is charged into the other side of converter and slag-making agent is not substantially charged and the decarburization is mainly executed within a prescribed time. When Si content in the molten iron is >0.3wt.%, the Si content is preliminary refined into <=0.3wt.%.

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、一の転炉において
溶銑の脱燐精錬を行い、この脱燐精錬された溶銑を他の
一以上の転炉において一の転炉における脱燐精錬時間内
において脱炭精錬を行い、円滑に連続した生産性の高い
溶銑からの製鋼方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to dephosphorization and refining of hot metal in one converter, and the dephosphorized and refined hot metal in one or more other converters within the dephosphorization and refining time in one converter. The present invention relates to a method for producing steel from hot metal with continuous and high productivity by performing decarburization refining.

【0002】[0002]

【従来の技術】伝統的転炉製鋼法においては、同一の転
炉において溶銑の脱燐精錬と脱炭精錬とを行なって、製
鋼作業を行っていた。しかし、近年の鋼材の品質に対す
る要求が高くなる一方、連続鋳造の拡大や、真空脱ガ
ス、取鍋精錬等の溶鋼の二次精錬が普及するに伴い、転
炉における出鋼温度が上昇し、転炉に於ける脱燐能力が
低下してきた。この理由は、脱燐反応は高温ほど不利に
進行するからである。
2. Description of the Related Art In a conventional converter steelmaking method, dephosphorizing and decarburizing refining of hot metal are performed in the same converter to perform steelmaking. However, while the demand for steel quality in recent years has increased, with the expansion of continuous casting, vacuum degassing, and secondary refining of molten steel such as ladle refining, the tapping temperature in converters has increased, The dephosphorization capacity in the converter has been reduced. The reason for this is that the dephosphorization reaction proceeds disadvantageously as the temperature increases.

【0003】そこで、転炉に装入する溶銑を予め処理し
て、特に燐(P)成分をある程度除去してから転炉に装
入する溶銑予備処理法が発展してきた。この方法の一つ
として、一の転炉等において溶銑の脱燐精錬を行ない、
この脱燐された溶銑を他の転炉に移動して脱炭精錬を行
なう製鋼法が実施されている。
[0003] Therefore, a hot metal pretreatment method has been developed in which the hot metal charged into the converter is preliminarily treated, and in particular, the phosphorus (P) component is removed to some extent before the hot metal is charged into the converter. As one of the methods, dephosphorizing and refining hot metal in one converter etc.
A steelmaking method in which the dephosphorized hot metal is transferred to another converter to perform decarburization refining has been implemented.

【0004】かかる技術として、特公平4−38810
号公報、特公平2−14404号公報、特公昭61−2
3243号公報の提案がある。また、本願の発明者も既
に従来の製鋼工場を改造し、複数の転炉のそれぞれの炉
前作業床に作業床開口部を設け、一の転炉で溶銑の脱燐
精錬をした溶湯を受湯鍋に受け、この受湯鍋を前記作業
床開口部を通して他の一の転炉に運搬し、この転炉に装
入し、ここで脱炭精錬を行なう精錬方法を開発している
(特開平6−41624号公報)。
As such a technique, Japanese Patent Publication No. 4-38810 is disclosed.
JP, JP-B2-14404, JP-B-61-2
There is a proposal of 3243 gazette. In addition, the inventor of the present application has also remodeled a conventional steelmaking plant, provided working floor openings in the working floor in front of each of a plurality of converters, and received molten metal obtained by dephosphorizing hot metal in one converter. A refining method has been developed in which a hot pot is received, and the hot pot is transported to another converter through the opening of the work floor, charged into the converter, and decarburized and refined therein (Japanese Patent Laid-Open No. Hei 6 (1994)). -41624).

【0005】[0005]

【発明が解決しようとする課題】上記製鋼方法におい
て、一の転炉等で溶銑の脱燐精錬を行ない直ちに出湯
し、これを他の転炉等で少なくとも脱燐精錬時間以内で
の時間内で脱炭精錬することが円滑な製鋼作業上必要で
ある。
In the above steelmaking method, the hot metal is dephosphorized and refined in one converter and the like, and the hot water is immediately discharged in another converter and the like within at least the dephosphorization and refining time. Decarburization and refining are necessary for smooth steelmaking operations.

【0006】本発明前における340ton転炉におけ
る脱燐精錬の概要を図11に示す。上記溶銑の脱燐精錬
は低温(1250〜1400℃)で行われており、ま
た、溶銑の脱燐精錬のためにスラグのFeO(5〜10
%)を高くするため、スラグがフォーミングしており、
直ちに出湯すると、炉口からスラグが流出し、又は受湯
鍋に大量のスラグが流入するので、図に示す様な鎮静時
間が4分程度を要していた。そのため、脱燐精錬時間
は、例えば平均約36分であった。
FIG. 11 shows an outline of dephosphorization refining in a 340 ton converter before the present invention. The dephosphorization and refining of the hot metal is performed at a low temperature (1250-1400 ° C.), and the slag FeO (5-10
%), The slag is formed,
Immediately after tapping, the slag flows out of the furnace port or a large amount of slag flows into the hot pot, so that the sedation time as shown in the figure required about 4 minutes. Therefore, the dephosphorization refining time was, for example, about 36 minutes on average.

【0007】一方、この脱燐溶銑の他の転炉における脱
炭精錬時間は種々の改良により平均29分、スラグコー
テイングをしない場合には27分である。従って、脱炭
精錬炉は少なくとも7分、最大9分遊び時間が発生し、
従ってその分製鋼能率が低下していた。この7分間の遊
び時間を短縮すると約20%の生産向上が得られる。ま
た、この遊び時間において脱炭精錬炉の炉内温度の低下
があり、煉瓦の損耗等も発生し、転炉寿命の低下ももた
らしていた。
On the other hand, the decarburization refining time of this dephosphorized hot metal in another converter is 29 minutes on average due to various improvements, and is 27 minutes without slag coating. Therefore, the decarburization smelting furnace has at least 7 minutes, up to 9 minutes idle time,
Therefore, the steel making efficiency was reduced accordingly. Reducing the 7 minute play time results in about a 20% increase in production. In addition, during this idle time, the temperature inside the decarburization refining furnace was lowered, bricks were worn, etc., and the converter life was shortened.

【0008】そこで、本発明は、脱燐精錬時間を低下さ
せ、脱炭精錬炉の遊び時間を無くし、円滑な製鋼作業を
確保し、更に製鋼能率の向上を目的とする。上記脱燐精
錬において溶鋼のP含有量を粗鋼成分のP含有量(所謂
規格値、通常0.02wt%以下)以下に精錬し、脱炭
精錬においては実質的に脱燐精錬をせず、製鋼能率の向
上を目的とする。
Accordingly, an object of the present invention is to reduce the dephosphorization refining time, eliminate idle time in the decarburization refining furnace, ensure a smooth steelmaking operation, and improve the steelmaking efficiency. In the above dephosphorizing refining, the P content of the molten steel is refined to the P content of the crude steel component (a so-called standard value, usually 0.02 wt% or less), and in the decarburizing refining, substantially no dephosphorizing refining is performed. The aim is to improve efficiency.

【0009】[0009]

【課題を解決するための手段】上記課題について種々研
究した結果、溶銑のSi含有量が低いほど脱燐精錬が進
行し、特にSiが0.3wt%以下の場合には、P含有
量を通常の粗鋼成分のP含有量(所謂規格値、通常0.
02wt%以下)まで精錬でき、脱炭精錬において実質
的に脱炭精錬のみを行うことにより達成できることを知
見し、下記の発明をするに至った。
As a result of various studies on the above-mentioned problems, the lower the Si content of the hot metal, the more the dephosphorization refining proceeds. Particularly, when the Si content is 0.3 wt% or less, the P content is usually reduced. P content of the crude steel component (so-called standard value, usually 0.1%).
(Less than 02 wt%), and found that the decarburization smelting can be achieved by substantially performing only decarburization smelting, and led to the following invention.

【0010】第1の発明は、下記の工程を備えたことを
特徴とする複数の転炉を使用する製鋼方法である。 (a)一の転炉において溶銑のSi含有量が0.3wt
%未満の溶銑を所定の時間内に脱燐精錬し、溶銑のP含
有量を粗鋼で要求されているP含有量(鋼の成分規格
値)以下に精錬し、(b)前記脱燐精錬された溶銑を他
の一以上の転炉に装入し、実質的に造滓材を装入せず前
記所定の時間内に主に脱炭精錬を行う。
A first invention is a steel making method using a plurality of converters, comprising the following steps. (A) In one converter, the Si content of the hot metal is 0.3 wt.
% Of the hot metal is dephosphorized and refined within a predetermined time, and the P content of the hot metal is refined to the P content (specified component value of steel) required for the crude steel. The hot metal is charged into one or more other converters, and decarburization refining is mainly performed within the predetermined time without substantially charging slag-making material.

【0011】上記発明においては、脱燐精錬において溶
銑のP含有量は粗鋼のP含有量(鋼の成分規格値)まで
精錬されているので、脱炭精錬においてはPを精錬する
ための焼石灰等の造滓材を装入する必要がなく、主に脱
炭精錬を行うので極めて簡素化でき、精錬時間も短縮で
きる。また、脱燐精錬するに際して、Si含有量が0.
3wt%以下の溶銑を使用しているので、スラグ発生量
が少なく、主にスラグの鎮静時間を無くすことができる
と共に、また、排滓時間が短縮でき、脱燐精錬時間を短
縮できるため、全体として製鋼能率を向上できる。
In the above invention, the P content of the hot metal is refined to the P content of the crude steel (specified value of the steel component) in the dephosphorization refining, so that in the decarburization refining, calcined lime for refining the P is refined. It is not necessary to insert a slag-making material, etc., and the decarburization refining is mainly performed, so that it can be extremely simplified and the refining time can be shortened. Further, when performing the dephosphorization refining, the Si content is set to 0.1.
Since the hot metal of 3 wt% or less is used, the amount of slag generated is small, and the slag calming time can be mainly eliminated. In addition, the waste time can be shortened and the dephosphorizing refining time can be shortened. Steelmaking efficiency can be improved.

【0012】第2の発明は、前記溶銑のSi含有量が
0.3wt%を超える場合には、予めSi含有量を0.
3wt%以下に予備精錬することを特徴とする複数の転
炉を使用する製鋼方法である。
According to a second aspect of the present invention, when the Si content of the hot metal exceeds 0.3% by weight, the Si content is set to 0.1% in advance.
This is a steel making method using a plurality of converters, which is characterized by preliminarily refining to 3 wt% or less.

【0013】高炉から得られる溶銑は通常Si含有量が
0.3wt%以下であるが、高炉操業が不安定になると
0.3wt%を超えることがある。この場合には溶銑の
Si含有量を0.3wt%以下に予備精錬し、脱燐精錬
時間を可及的に短縮できる。
[0013] Hot metal obtained from a blast furnace usually has a Si content of 0.3 wt% or less, but may exceed 0.3 wt% if the operation of the blast furnace becomes unstable. In this case, the pre-refining is performed to reduce the Si content of the hot metal to 0.3 wt% or less, and the time for dephosphorizing refining can be reduced as much as possible.

【0014】[0014]

【発明の実施の形態】本発明においては転炉(349t
on)において図1に示すような脱燐精錬を行う。スク
ラップを装入後、高炉からの溶銑を装入し、酸素吹錬を
開始し、焼石灰、螢石、鉄鉱石等を装入しながら精錬を
行う。酸素吹錬が終了するとリンスを行い出湯する。
DESCRIPTION OF THE PREFERRED EMBODIMENTS In the present invention, a converter (349 t)
On), dephosphorization refining as shown in FIG. 1 is performed. After charging the scrap, the hot metal from the blast furnace is charged, oxygen blowing is started, and refining is performed while charging calcined lime, fluorite, iron ore, and the like. When the oxygen blowing is completed, a rinse is performed and hot water is discharged.

【0015】上記吹錬において、溶銑の脱燐精錬に与え
る溶銑のSi含有量の影響を図2から図7において説明
する。図2には脱燐精錬において装入又は添加したCa
O量と溶銑のSi含有量から計算で求められる塩基度
(CaOwt%/SiO2 wt%,図ではC/Sと表示
する)とスラグの分析から得られた塩基度との関係を示
す。この図から溶銑にSi含有量が高いほど計算塩基度
(C/S)と分析塩基度の解離が大きい、CaOが有効
に脱燐反応に作用していないことが判る。
The effect of the Si content of the hot metal on the dephosphorization refining of the hot metal in the above blowing will be described with reference to FIGS. FIG. 2 shows Ca added or added in the dephosphorization refining.
O amount and the hot metal basicity is calculated from the Si content of the (CaOwt% / SiO 2 wt% , indicated as C / S in the figure) to indicate the relationship between the obtained basicity derived from the analysis of the slag. From this figure, it can be seen that the higher the Si content in the hot metal, the greater the dissociation of the calculated basicity (C / S) and the analytical basicity. CaO is not effectively acting on the dephosphorization reaction.

【0016】また、図3には略同一塩基度における溶銑
のSi含有量とPの分配率(LP =(P)/[P])と
の関係を示す。Si含有量が低い程LP が高いことを示
す。即ち、恐らくSi含有量が低い程均一なスラグが生
成されているためと推定される。
FIG. 3 shows the relationship between the Si content of the hot metal and the distribution ratio of P (L P = (P) / [P]) at substantially the same basicity. The lower Si content indicates that L P is high. That is, it is presumed that the lower the Si content is, the more uniform slag is generated.

【0017】図4には、例えばPを0.02wt%以下
に精錬する精錬時間と溶銑のSi含有量との関係を示
す。Si含有量が低い程精錬時間が短縮されることを示
す。更に、図5にはSi含有量が0.3wt%である場
合における脱燐精錬時間を具体的に示す。
FIG. 4 shows the relationship between the refining time for refining P to 0.02 wt% or less and the Si content of the hot metal, for example. The lower the Si content, the shorter the refining time. FIG. 5 specifically shows the dephosphorization refining time when the Si content is 0.3 wt%.

【0018】図6には溶銑のSi含有量と脱燐精錬処理
後のP含有量との関係を示す。溶銑のSi含有量が低い
ほど脱燐精錬処理後のP含有量が低いことを示す。 更
に、図7は、溶銑のSi含有量は低いほど一日当たりの
脱燐精錬チャージ(チャージ/日)が高い、即ち生産性
が高くなることを示す。
FIG. 6 shows the relationship between the Si content of the hot metal and the P content after the dephosphorization refining process. The lower the Si content of the hot metal, the lower the P content after the dephosphorization refining treatment. Further, FIG. 7 shows that the lower the Si content of the hot metal, the higher the dephosphorization refining charge per day (charge / day), that is, the higher the productivity.

【0019】脱燐精錬が終了した脱燐溶銑は他の転炉に
装入され、図8に示すような脱炭精錬が行われ最終的に
予め定められた鋼にされる。この脱炭精錬は、主に鋼中
の炭素を酸素吹錬して目的とする炭素含有量とする精錬
である。原則としては焼石灰等の造滓材は装入せず、鉄
源となる鉄鉱石、スケール等を装入する。
The dephosphorized hot metal that has been dephosphorized and refined is charged into another converter and decarburized and refined as shown in FIG. 8 to finally produce a predetermined steel. This decarburization refining is refining mainly by subjecting carbon in steel to oxygen blowing to obtain a target carbon content. In principle, slag-making materials such as calcined lime are not charged, but iron ore, scale, etc., which are iron sources, are charged.

【0020】溶銑は既に十分脱燐されているので、吹錬
中においてマンガン鉱石を装入して溶鋼のMn含有量を
高くし、高価なマンガン合金を節約する。但し、脱燐溶
銑のP含有量が粗鋼で要求されているP含有量(鋼の成
分規格値)以上の場合には、焼石灰等の造滓材を装入す
ることを排除するものではい。
Since the hot metal has already been sufficiently dephosphorized, manganese ore is charged during blowing to increase the Mn content of the molten steel and save expensive manganese alloys. However, if the P content of the dephosphorized hot metal is equal to or higher than the P content (specified component value of steel) required for crude steel, it does not exclude charging of slag-making material such as calcined lime. .

【0021】更に、上記脱炭精錬においては、脱炭精錬
炉の寿命を最大限とするため、脱燐溶銑を装入するに先
立ち予め軽焼ドロマイト及び/又は生ドロマイトを添加
することができる。そして、脱炭精錬中において十分ス
ラグに溶解し、MgO濃度を10wt%以上とする。こ
のようなスラグはスラグ自体がMgOを溶解度限まで含
有しているため、マグネシヤ(MgO)煉瓦からなる炉
体煉瓦の損耗を抑制し、炉体寿命を延長させる効果があ
る。
Further, in the above-mentioned decarburization refining, in order to maximize the life of the decarburization refining furnace, lightly-burned dolomite and / or raw dolomite can be added before charging the dephosphorized hot metal. Then, during the decarburization refining, it is sufficiently dissolved in the slag, and the MgO concentration is set to 10 wt% or more. Since such slag itself contains MgO up to the solubility limit, the slag has an effect of suppressing wear of the furnace body brick made of magnesium (MgO) brick and extending the life of the furnace body.

【0022】さらに、溶鋼を出鋼後において炉体を傾動
して炉内に残留したスラグを炉体内張り煉瓦に付着さ
せ、所謂スラグコーテイングを行う。このスラグコーテ
イングは炉体寿命の延長に大きく貢献し、脱燐精錬炉と
同程度の炉体寿命となる。従って、脱燐精錬時間と脱炭
精錬時間の時間的サイクルが同じとなるだけでなく、双
方の炉体寿命も同程度になり円滑な一貫した製鋼作業が
可能となる。
Further, after the molten steel is tapped, the furnace body is tilted so that the slag remaining in the furnace adheres to the brick in the furnace, so-called slag coating is performed. This slag coating greatly contributes to prolonging the life of the furnace, and the life of the furnace is about the same as that of the dephosphorizing smelting furnace. Therefore, not only the time cycle of the dephosphorization refining time and the decarburization refining time become the same, but also the furnace life of both furnaces becomes the same, and a smooth and consistent steelmaking operation becomes possible.

【0023】脱炭精錬時間は約29分間である。前述の
通り脱燐精錬は溶銑のSi含有量により変化する。そこ
で本発明においては溶銑のSi含有量は少なくとも0.
3wt%以下とする。可能なかぎり脱炭精錬時間の時間
差を少なくするためである。溶銑のSi含有量が、0.
2wt%以下であることはより望ましい。しかし、Si
含有量が0.05wt%未満では脱燐精錬をするための
スラグが生成されないので望ましくない。
The decarburization refining time is about 29 minutes. As described above, the dephosphorization refining changes depending on the Si content of the hot metal. Therefore, in the present invention, the Si content of the hot metal is at least 0.1.
3 wt% or less. This is to reduce the time difference between the decarburization refining times as much as possible. When the Si content of the hot metal is 0.
It is more desirable that the content be 2 wt% or less. However, Si
If the content is less than 0.05% by weight, slag for dephosphorization refining is not generated, which is not desirable.

【0024】本発明では、0.3wt%以下の溶銑を使
用するが、定常的な高炉操業ではSiが0.3wt%以
下であるので問題はない。しかし、非定常的な操業(高
炉休風後)ではSiが0.3wt%を超えることがある
が、このような場合には溶銑鍋等で予め脱珪素を行う。
In the present invention, hot metal of 0.3 wt% or less is used, but there is no problem in steady blast furnace operation because Si is 0.3 wt% or less. However, in an unsteady operation (after the blast furnace is shut down), Si may exceed 0.3 wt%. In such a case, silicon removal is performed in advance using a hot metal pot or the like.

【0025】更に、本発明において、2基以上の転炉を
使用することができる。即ち、前述の通り、本発明は少
なくとも略同一容量の2基の転炉において実施すること
ができる。しかし、例えば340tonの脱燐精錬炉1
基と、170ton容量の脱炭精錬炉を2基組み合わせ
てもよい。脱炭精錬は粗鋼のC成分により異なる精錬を
することが望ましい。そこで、脱炭精錬炉を1基或いは
2基以上備えても本発明は実施できる。
Further, in the present invention, two or more converters can be used. That is, as described above, the present invention can be practiced in at least two converters having substantially the same capacity. However, for example, a 340 ton dephosphorization refining furnace 1
And two 170-ton decarburization refining furnaces. In the decarburization refining, it is desirable to perform different refining depending on the C component of the crude steel. Therefore, the present invention can be implemented even if one or two or more decarburization refining furnaces are provided.

【0026】また、上記において転炉とは所謂酸素上吹
き転炉のみならず、転炉型の精錬容器、例えば上底吹き
転炉、底吹き転炉を含む概念である。これらの各種の転
炉において実施できることはいうまでもない。
In the above description, the converter is a concept including not only a so-called oxygen top-blowing converter but also a converter type refining vessel such as a top-bottom blowing converter and a bottom-blowing converter. It goes without saying that it can be carried out in these various converters.

【0027】[0027]

【実施例】本発明の方法により、低炭素鋼(C:0.1
wt%以下)、中炭素鋼(C:0.1〜0.2wt
%)、高炭素鋼(C:0.3wt%以上)をそれぞれ5
0チャージ製造し、上記脱燐精錬、及び脱炭精錬におけ
る成分組成の変化を図9及び図10に示す。溶銑のSi
含有量が低い程脱燐精錬後のP含有量が低く、通常の粗
鋼で要求されるP含有量(規格値)まで低下しており、
脱炭精錬においては全く脱燐を行う必要がなかった。ま
た、既に述べたように脱燐精錬時間は平均32.2分、
脱炭精錬時間は平均29分であり、脱燐精錬した溶銑は
円滑に脱炭精錬することができ、鋼を連続的に生産でき
た。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Low carbon steel (C: 0.1
wt% or less), medium carbon steel (C: 0.1-0.2wt)
%) And high carbon steel (C: 0.3 wt% or more)
FIGS. 9 and 10 show the changes in the component compositions in the above-mentioned dephosphorization refining and decarburization refining after zero charge production. Hot metal Si
The lower the content, the lower the P content after dephosphorization refining, and the lower the P content (standard value) required for ordinary crude steel,
In the decarburization refining, there was no need to perform dephosphorization at all. In addition, as described above, the dephosphorization refining time averaged 32.2 minutes,
The decarburization refining time was 29 minutes on average, and the dephosphorized and refined hot metal could be smoothly decarburized and refined, and steel could be continuously produced.

【0028】[0028]

【発明の効果】本発明においては、Si含有量が0.3
wt%以下の溶銑を脱燐精錬し、この溶銑を脱炭精錬す
ることにより、従来、脱炭精錬時間より長かった脱燐精
錬を短縮でき、スラグコーテイング時間を含めた脱炭精
錬時間により近づくことができる。従って全体として所
謂製鋼時間を約20%短縮することができる。
According to the present invention, the Si content is 0.3%.
By dephosphorizing and refining hot metal of less than wt% and decarburizing and refining this hot metal, the dephosphorizing refining, which was longer than the conventional decarburizing refining time, can be shortened and approaching the decarburizing refining time including the slag coating time. Can be. Therefore, the so-called steel making time can be reduced by about 20% as a whole.

【0029】また、脱炭精錬においては脱燐をする必要
が無くなったので、安価なMn鉱石を最大限使用するこ
とができ、高価なマンガン合金を節約できるので、従来
よりもより経済的に鋼の製造ができる。更に、脱炭精錬
炉の炉体寿命が脱燐精錬炉と同程度になるため、同時に
炉体修理を行うことができ円滑な製鋼作業ができる。こ
れらの効果は極めて大きく、生産能率の向上は甚大であ
り、産業上の効果は著しい。
Further, in the decarburization refining, the need for dephosphorization is eliminated, so that inexpensive Mn ore can be used to the maximum and expensive manganese alloys can be saved, so that steel can be more economically produced than before. Can be manufactured. Further, since the life of the furnace body of the decarburizing smelting furnace is almost the same as that of the dephosphorizing smelting furnace, the furnace body can be repaired at the same time, and a smooth steelmaking operation can be performed. These effects are extremely large, the production efficiency is greatly improved, and the industrial effects are remarkable.

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

【図1】本発明における脱燐精錬工程の全体を示す図で
ある。
FIG. 1 is a diagram showing the entire dephosphorization refining process in the present invention.

【図2】脱燐精錬における配合塩基度と実績塩基度との
関係を示す図である。
FIG. 2 is a diagram showing the relationship between the blended basicity and the actual basicity in dephosphorization refining.

【図3】脱燐精錬におけるSi含有量と燐の分配率との
関係を示す図である。
FIG. 3 is a diagram showing the relationship between the Si content and the distribution rate of phosphorus in dephosphorization refining.

【図4】脱燐精錬におけるSi含有量と脱燐精錬時間と
の関係を示す図である。
FIG. 4 is a diagram showing a relationship between a Si content and a dephosphorization refining time in dephosphorization refining.

【図5】Si含有量が0.3wt%における脱燐精錬時
間を示す図である。
FIG. 5 is a diagram showing a dephosphorization refining time at a Si content of 0.3 wt%.

【図6】溶銑のSi含有量と脱燐精錬後の燐含有量との
関係を示す図である。
FIG. 6 is a graph showing the relationship between the Si content of hot metal and the phosphorus content after dephosphorization refining.

【図7】脱燐精錬におけるSi含有量と一日のチャージ
数を示す図である。
FIG. 7 is a diagram showing the Si content and the number of charges per day in dephosphorization refining.

【図8】脱炭精錬の全工程を示す図である。FIG. 8 is a view showing all the steps of decarburization refining.

【図9】本発明の脱燐精錬を低炭素鋼(C:0.1wt
%以下)、中炭素鋼(C:0.1〜0.2wt%)、高
炭素鋼のそれぞれに適用した場合における成分組成の変
化を示す図である。
FIG. 9 shows that the dephosphorization refining of the present invention is carried out using a low carbon steel (C: 0.1 wt.
% Or less), medium carbon steel (C: 0.1 to 0.2 wt%), and a diagram showing a change in component composition when applied to high carbon steel.

【図10】本発明の脱炭精錬を低炭素鋼(C:0.1w
t%以下)、中炭素鋼(C:0.1〜0.2wt%)、
高炭素鋼のそれぞれに適用した場合における成分組成の
変化を示す図である。
[FIG. 10] The decarburization refining of the present invention is performed using low carbon steel (C: 0.1 w
t% or less), medium carbon steel (C: 0.1 to 0.2 wt%),
It is a figure which shows the change of a component composition at the time of applying to each of high carbon steel.

【図11】本発明前の脱燐精錬の工程を示す図である。FIG. 11 is a view showing a dephosphorization refining process before the present invention.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 小平 悟史 東京都千代田区丸の内一丁目1番2号 日 本鋼管株式会社内 (72)発明者 菊地 一郎 東京都千代田区丸の内一丁目1番2号 日 本鋼管株式会社内 (72)発明者 新井 学 東京都千代田区丸の内一丁目1番2号 日 本鋼管株式会社内 (72)発明者 田中 秀栄 東京都千代田区丸の内一丁目1番2号 日 本鋼管株式会社内 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Satoshi Kodaira 1-2-1, Marunouchi, Chiyoda-ku, Tokyo, Japan Inside Nihon Kokan Co., Ltd. (72) Inventor Ichiro Kikuchi 1-2-1, Marunouchi, Chiyoda-ku, Tokyo, Japan (72) Inventor Manabu Arai, 1-2-1, Marunouchi, Chiyoda-ku, Tokyo, Japan Nihon Kokan Co., Ltd. (72) Hideei Tanaka 1-2-1, Marunouchi, Chiyoda-ku, Tokyo, Japan Inside the corporation

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 下記の工程を備えたことを特徴とする複
数の転炉を使用する製鋼方法。 (a)一の転炉において溶銑の珪素(以下Siと記す
る)含有量が0.3wt%以下の溶銑を所定の時間内に
脱燐精錬し、溶銑の燐(以下Pと記する)含有量を粗鋼
で要求されているP含有量(鋼の成分規格値)以下に精
錬し、(b)前記脱燐精錬された溶銑を他の一以上の転
炉に装入し、実質的に造滓材を装入せず前記所定の時間
以内に主に脱炭精錬を行う。
1. A steel making method using a plurality of converters, comprising the following steps. (A) In one converter, hot metal whose content of silicon (hereinafter, referred to as Si) in the hot metal is 0.3 wt% or less is dephosphorized and refined within a predetermined time, and the hot metal contains phosphorus (hereinafter, referred to as P). Refining the amount to below the P content required for crude steel (specification of steel components), and (b) charging the dephosphorized and refined hot metal into one or more other converters to substantially form Decarburization refining is mainly performed within the above-mentioned predetermined time without charging slag material.
【請求項2】 前記溶銑のSi含有量が0.3wt%を
超える場合には、予めSi含有量を0.3wt%以下に
予備精錬することを特徴とする請求項1記載の複数の転
炉を使用する製鋼方法。
2. A plurality of converters according to claim 1, wherein when the Si content of the hot metal exceeds 0.3 wt%, the pre-refining is performed in advance to reduce the Si content to 0.3 wt% or less. Use steel making method.
JP06739197A 1997-03-05 1997-03-05 Steelmaking method using multiple converters Expired - Fee Related JP3486887B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06739197A JP3486887B2 (en) 1997-03-05 1997-03-05 Steelmaking method using multiple converters

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06739197A JP3486887B2 (en) 1997-03-05 1997-03-05 Steelmaking method using multiple converters

Publications (2)

Publication Number Publication Date
JPH10245617A true JPH10245617A (en) 1998-09-14
JP3486887B2 JP3486887B2 (en) 2004-01-13

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ID=13343644

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Country Status (1)

Country Link
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002363630A (en) * 2001-06-06 2002-12-18 Nippon Steel Corp Method for preliminary treatment of converter hot metal
JP2013007117A (en) * 2011-05-23 2013-01-10 Jfe Steel Corp Method of producing molten steel

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002363630A (en) * 2001-06-06 2002-12-18 Nippon Steel Corp Method for preliminary treatment of converter hot metal
JP4718722B2 (en) * 2001-06-06 2011-07-06 新日本製鐵株式会社 Converter type hot metal pretreatment method
JP2013007117A (en) * 2011-05-23 2013-01-10 Jfe Steel Corp Method of producing molten steel

Also Published As

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