JPH0499216A - Production of al-free weakly deoxidized steel - Google Patents

Production of al-free weakly deoxidized steel

Info

Publication number
JPH0499216A
JPH0499216A JP2212672A JP21267290A JPH0499216A JP H0499216 A JPH0499216 A JP H0499216A JP 2212672 A JP2212672 A JP 2212672A JP 21267290 A JP21267290 A JP 21267290A JP H0499216 A JPH0499216 A JP H0499216A
Authority
JP
Japan
Prior art keywords
steel
treatment
free oxygen
less
free
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
JP2212672A
Other languages
Japanese (ja)
Other versions
JPH0733539B2 (en
Inventor
Kazuaki Tanaka
和明 田中
Shigenori Nishimori
西森 茂憲
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 JP2212672A priority Critical patent/JPH0733539B2/en
Publication of JPH0499216A publication Critical patent/JPH0499216A/en
Publication of JPH0733539B2 publication Critical patent/JPH0733539B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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

  • Treatment Of Steel In Its Molten State (AREA)

Abstract

PURPOSE:To minimize the rate of occurrence of UST unfit occurrence ratio by throwing quick lime before RH treatment to modify ladle slag, measuring free oxygen in a steel at intervals of several minutes in the course of RH degassing treatment, and throwing a weakly deoxidizing element at the point of time when the fall in the content of free oxygen in the steel begins to stop. CONSTITUTION:Quick lime is thrown into a ladle before RH treatment for a molten steel to regulate T.Fe in slag to <=2% and also to regulate Al and free oxygen in the steel to <=0.001% and <=100ppm, respectively. In the course of RH treatment, degassing treatment is performed until free oxygen in the steel reaches <=50ppm and then Ti (Zr) is thrown. Further, after RH treatment, Al and free oxygen in the steel are regulated to <=10ppm and <=30ppm, respectively.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はAlレス弱脱酸鋼の製造方法に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention relates to a method for producing Al-free weakly deoxidized steel.

(従来の技術) 従来技術として、第1図に示す従来法で説明する。鋼の
変態核となる10m以下の微小酸化物の個数を増加させ
るため、RHの脱ガス処理中に、鋼中フリー酸素が11
00pp以上の時に、TiやZrなどの弱脱酸元素を投
入する。鋼中フリー酸素の値を制御するために、脱ガス
処理にOB処理を行い、続いてAl投入を行う。
(Prior Art) As a prior art, a conventional method shown in FIG. 1 will be explained. In order to increase the number of micro oxides of 10 m or less that serve as transformation nuclei in steel, during the RH degassing treatment, free oxygen in the steel was reduced to 11
When the amount is 00 pp or more, a weak deoxidizing element such as Ti or Zr is added. In order to control the value of free oxygen in the steel, OB treatment is performed for degassing treatment, followed by Al injection.

(発明が解決しようとする課B) 本発明の課題を、従来法を示す第2図により説明する。(Problem B that the invention attempts to solve) The problem of the present invention will be explained with reference to FIG. 2, which shows a conventional method.

微小酸化物の個数を増加させるために、RH脱ガス処理
中に、鋼中フリー酸素が100ppm以上で弱脱酸元素
を投入する従来法を実施すると、弱脱酸元素と平衡にな
るまで、鋼中フリー酸素が減少し、従来法に示すように
、Al、03やTiO系の脱酸生成物量が増加し、これ
が鋳片上面側に集積し、UST不台の原因となる。
In order to increase the number of micro oxides, when the conventional method of adding a weak deoxidizing element during RH degassing treatment when the free oxygen in the steel is 100 ppm or more is carried out, the steel Free oxygen in the steel decreases, and as shown in the conventional method, the amount of Al, 03, and TiO-based deoxidation products increases, which accumulates on the upper surface of the slab and causes UST failure.

(課題を解決するための手段) 本発明は前記の課題を有利に解決するものであって、そ
の要旨は溶鋼のRH処理前に、取鍋内に生石灰を投入し
、スラグ中のT、 Feを2%以下にならしめ、へ!;
0.001%以下で鋼中フリー酸素を1100pp以下
にし、RH処理中には、脱ガスにより鋼中フリー酸素を
50ppm以下まで処理し、その後↑j (Zr)を投
入し、RH処理後には、Al;10ppo+以下で鋼中
フリー酸素を30ppm以下とすることを特徴とするA
lレス弱脱酸鋼の製造方法にある。
(Means for Solving the Problems) The present invention advantageously solves the above-mentioned problems, and the gist thereof is that before the RH treatment of molten steel, quicklime is charged into a ladle, and T, Fe in the slag is Keep it below 2% and go! ;
At 0.001% or less, the free oxygen in the steel is reduced to 1100 ppm or less, and during the RH treatment, the free oxygen in the steel is reduced to 50 ppm or less by degassing, and then ↑j (Zr) is introduced, and after the RH treatment, A characterized in that Al: 10 pp+ or less and free oxygen in the steel is 30 ppm or less
A method for manufacturing l-less weakly deoxidized steel.

以下図面に基づいて本発明を説明する。The present invention will be explained below based on the drawings.

本発明で用いる鋼種の成分系を表1(最終製品の成分系
)で示す。特にAIに間しては、AI末脱酸状態であり
、TiはOとNにバランスするように微量添加する。
Table 1 (composition system of final product) shows the composition of the steel used in the present invention. In particular, the AI is in a deoxidized state, and a small amount of Ti is added to balance O and N.

本発明の方法を第1図で説明する。RH脱ガス処理中に
、OB処理を行なわず、またA!投入を行わず、またA
Iの混入の原因となる組成中にAlを含む合金元素の添
加は、RH肌脱ガス処理前行う。
The method of the invention will be explained with reference to FIG. During RH degassing treatment, OB treatment was not performed and A! No input, and A
Addition of an alloying element containing Al in the composition, which causes I contamination, is performed before the RH skin degassing treatment.

また、RH処理前に、住石灰を投入し、取鍋スラグの改
質を行う。RH脱ガス処理中に、数分毎に鋼中フリー酸
素を測定し、鋼中フリー酸素の降下がなくなり始めた時
点で弱脱酸元素を投入する。
Furthermore, before the RH treatment, limestone is added to reform the ladle slag. During the RH degassing treatment, the free oxygen in the steel is measured every few minutes, and a weak deoxidizing element is added when the free oxygen in the steel starts to stop dropping.

本発明の方法の効果を本発明を示す第2図で説明する。The effect of the method of the invention will be explained with reference to FIG. 2, which shows the invention.

弱脱酸元素の投入時の酸素値が低いため、TiO系の脱
酸生成物量が減少し、tJsT不合となる鋳片上面側に
集積する介在物が減少する。
Since the oxygen value at the time of introducing the weak deoxidizing element is low, the amount of TiO-based deoxidizing products decreases, and the number of inclusions that accumulate on the upper surface side of the slab, which causes tJsT failure, decreases.

本発明の方法を可能とさせた考え方を以下に示す。The idea that made the method of the present invention possible is shown below.

鋼の変態核となる微小酸化物の生成理論より、鋼中so
1.AIが10ppm以下の状態では、凝固温度で弱脱
酸元素と平衡する酸素値が10μ以下の酸化物個数を決
めるため、RH脱ガス処理での弱脱酸元素投入から鋳片
凝固までの脱酸生成物量には微小酸化物個数は影響しな
いことが判明した。また、UST不台の発生原因が脱酸
材投入時点から凝固時点までに成長した脱酸生成物が介
在物となっていることであることが介在物組成分析結果
より判明した。そこで、Alレス弱脱酸鋼の製造におい
ては、鋼中so1.AIをI Oppm以下および鋼中
フリー酸素をl OOppra以下を目標さした。
Based on the theory of the formation of micro oxides that serve as transformation nuclei in steel, the so
1. When AI is 10 ppm or less, in order to determine the number of oxides with an oxygen value of 10μ or less that is in equilibrium with the weak deoxidizing element at the solidification temperature, deoxidation is necessary from the addition of the weak deoxidizing element in the RH degassing treatment to the solidification of the slab. It was found that the number of micro oxides did not affect the amount of products. In addition, the inclusion composition analysis results revealed that the cause of UST failure was inclusions formed by deoxidation products that grew from the time when the deoxidizer was added to the time when it solidified. Therefore, in the production of Al-free weakly deoxidized steel, so1. The aim was to keep the AI below IOppm and the free oxygen in the steel below 1OOppra.

(発明の効果) 第3図は、従来法と本発明法のUST不合発生率を示し
たものであるが、本発明により、UST不合発生率はほ
とんど皆無となった。
(Effects of the Invention) FIG. 3 shows the incidence of UST failure in the conventional method and the method of the present invention, and according to the present invention, the incidence of UST failure was almost completely eliminated.

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

第1図は、本発明によるRH脱ガス時間と鋼中フリー〔
0〕との関係を従来法と比較して示す図、第2図は、本
発明による脱酸生成物に消費される
Figure 1 shows the RH degassing time and the free temperature in steel according to the present invention.
0] compared with the conventional method, Figure 2 shows the relationship between

〔0〕の内訳を従来
法と比較して示す図、第3図はUST不合発生率を示す
図である。 第 2図 q線球〉 く44し明ち配)
FIG. 3 is a diagram showing the breakdown of [0] in comparison with the conventional method, and FIG. 3 is a diagram showing the UST failure occurrence rate. Figure 2 q-ray ball>

Claims (1)

【特許請求の範囲】[Claims] 溶鋼のRH処理前に、取鍋内に生石灰を投入し、スラグ
中のT.Feを2%以下にならしめ、Al;0.001
%以下で鋼中フリー酸素を100ppm以下にし、RH
処理中には、脱ガスにより鋼中フリー酸素を50ppm
以下まで処理し、その後Ti(Zr)を投入し、RH処
理後には、Al;10ppm以下で鋼中フリー酸素を3
0ppm以下とすることを特徴とするAlレス弱脱酸鋼
の製造方法。
Before RH treatment of molten steel, quicklime is put into the ladle to remove T. Fe leveled to 2% or less, Al; 0.001
% or less, the free oxygen in the steel is 100 ppm or less, and the RH
During treatment, free oxygen in the steel is reduced to 50 ppm by degassing.
After that, Ti (Zr) is added, and after the RH treatment, the free oxygen in the steel is reduced to 3 with Al: 10 ppm or less.
A method for producing Al-less weakly deoxidized steel, characterized in that the Al content is 0 ppm or less.
JP2212672A 1990-08-11 1990-08-11 Method for producing Al-less weakly deoxidized steel Expired - Fee Related JPH0733539B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2212672A JPH0733539B2 (en) 1990-08-11 1990-08-11 Method for producing Al-less weakly deoxidized steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2212672A JPH0733539B2 (en) 1990-08-11 1990-08-11 Method for producing Al-less weakly deoxidized steel

Publications (2)

Publication Number Publication Date
JPH0499216A true JPH0499216A (en) 1992-03-31
JPH0733539B2 JPH0733539B2 (en) 1995-04-12

Family

ID=16626489

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2212672A Expired - Fee Related JPH0733539B2 (en) 1990-08-11 1990-08-11 Method for producing Al-less weakly deoxidized steel

Country Status (1)

Country Link
JP (1) JPH0733539B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20040046397A (en) * 2002-11-27 2004-06-05 주식회사 포스코 Degassing process of molten steel by making an analysis of slag

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5735243A (en) * 1980-08-11 1982-02-25 Kyokuto Denki Kk Hot air flow type heating apparatus
JPS621811A (en) * 1985-06-26 1987-01-07 Nippon Steel Corp Manufacture of rail having superior damage resistance

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5735243A (en) * 1980-08-11 1982-02-25 Kyokuto Denki Kk Hot air flow type heating apparatus
JPS621811A (en) * 1985-06-26 1987-01-07 Nippon Steel Corp Manufacture of rail having superior damage resistance

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20040046397A (en) * 2002-11-27 2004-06-05 주식회사 포스코 Degassing process of molten steel by making an analysis of slag

Also Published As

Publication number Publication date
JPH0733539B2 (en) 1995-04-12

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