JPH0347910A - Method for deoxidizing molten steel - Google Patents

Method for deoxidizing molten steel

Info

Publication number
JPH0347910A
JPH0347910A JP18046689A JP18046689A JPH0347910A JP H0347910 A JPH0347910 A JP H0347910A JP 18046689 A JP18046689 A JP 18046689A JP 18046689 A JP18046689 A JP 18046689A JP H0347910 A JPH0347910 A JP H0347910A
Authority
JP
Japan
Prior art keywords
molten steel
cao
deoxidizing
deoxidation
added
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
Application number
JP18046689A
Other languages
Japanese (ja)
Inventor
Masahiro Osaki
大崎 眞宏
Naoki Konno
今野 直樹
Koji Wada
耕治 和田
Tadashi Imai
正 今井
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 JP18046689A priority Critical patent/JPH0347910A/en
Publication of JPH0347910A publication Critical patent/JPH0347910A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To effectively execute deoxidation in molten steel by adding combined body of metallic Al and CaO into molten steel, which is not yet deoxidized, and executing deoxidation with the generated inclusion as CaO-Al2O3 series composition. CONSTITUTION:Into the molten steel, which is not yet deoxidized, the combined body or mixed body of the metallic Al and CaO or metallic Al, CaO and CaF2 is added to execute the deoxidation with the generated inclusion as CaO-Al2O3 series composition. By this method, the molten steel is deoxidized and at the same time, the micro Al2O3 which is the cause of defect in the product is adsorbed to CaO, and UST defect, bulging, sliver, etc., in the product is drastically reduced.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は溶鋼の脱酸方法に関するものである。[Detailed description of the invention] (Industrial application field) The present invention relates to a method for deoxidizing molten steel.

(従来の技術) 溶鋼の脱酸方法としてアルミニウムキルド鋼と称する鋼
の場合、製鋼工程において一般的には未脱酸溶鋼の中に
純Mを添加して脱酸している。
(Prior Art) As a method for deoxidizing molten steel, in the case of steel called aluminum killed steel, pure M is generally added to undeoxidized molten steel to deoxidize it in the steel manufacturing process.

この脱酸方法であると脱酸生成物としてA720゜系の
酸化物が大量に発生する。この溶鋼内にミクロに懸濁分
散したM2O3はその後、モールド内又はモールドに至
るまでの間に凝集しA1203クラスターとなって鋳造
時鋳片に捕捉されると「スリバー」と称する表面疵とな
ったり、「ふくれ状欠陥」や「ブローホール」と称する
内部欠陥となって著しく鋼材の品質を悪化することが一
般によく知られている。このため通常脱酸以降の処理工
程でN2O3を浮上分離させ溶鋼と分離し、鋼材の欠陥
を減少させる方法が一般に行われている。
This deoxidation method generates a large amount of A720° series oxides as deoxidation products. The M2O3 microscopically suspended and dispersed in this molten steel then aggregates in the mold or before reaching the mold, forming A1203 clusters, and when captured in the slab during casting, it becomes a surface flaw called "sliver". It is generally well known that internal defects called "bulge-like defects" and "blowholes" occur, which significantly deteriorate the quality of steel materials. For this reason, a method is generally used in which N2O3 is floated and separated from the molten steel in a treatment step after deoxidation to reduce defects in the steel material.

例えば、a)IV脱酸後の溶鋼を撹拌、バブリング等し
てN z O3を凝集合体して浮上を促進する方法。
For example, a) a method of stirring, bubbling, etc. the molten steel after IV deoxidation to agglomerate and coalesce N z O3 to promote floating.

b)タンデイツシュの中に堰を設けてN z O3の浮
上を促進する方法(特開昭60−114513号公報)
、C)モールド内でのArガスの吹き込みによるN2O
3の浮上分離の促進方法(特開昭59−6313号公報
)等が知られている。
b) Method of promoting floating of N z O3 by providing a weir in the tandem tube (Japanese Patent Application Laid-open No. 114513/1983)
, C) N2O by blowing Ar gas inside the mold
Method 3 of promoting flotation separation (Japanese Unexamined Patent Publication No. 59-6313) is known.

(発明が解決しようとする課題) 従来行われている純M添加による脱酸方法では脱酸生成
物であるNz(hが大量に発生しその後の浮上分離アク
ションを実施しても十分でなく現状の脱酸方法、浮上分
離対策では鋼材の欠陥となるA/ z O3を皆無にす
るには至っていない。このため前述の7V203浮上分
離対策を実施した場合でも、lV2O3に起因する欠陥
がある程度発生しその根絶対策はまだ実施されていない
のが現状である。
(Problem to be solved by the invention) In the conventional deoxidation method by adding pure M, a large amount of Nz(h), which is a deoxidation product, is generated, and the subsequent flotation separation action is not sufficient. Deoxidization methods and flotation measures have not completely eliminated A/z O3, which causes defects in steel materials.For this reason, even if the aforementioned 7V203 flotation measures are implemented, defects due to lV2O3 will still occur to some extent. At present, measures to eradicate the disease have not yet been implemented.

(課題を解決するための手段) 本発明の要旨とするところは未脱酸の溶鋼中へ金属アル
ミニウム、CaO又は金属アルミニウム、Cab、 C
aF2の結合体又は、混合体を添加し、生成する介在物
をCab−A7zQ、、系組成とさせて脱酸することを
特徴とする溶鋼の脱酸方法にある。
(Means for Solving the Problems) The gist of the present invention is to add metal aluminum, CaO, or metal aluminum, Cab, C into undeoxidized molten steel.
A method for deoxidizing molten steel characterized by adding a combination or a mixture of aF2 and deoxidizing the generated inclusions to have a Cab-A7zQ system composition.

すなわち本発明は溶鋼を脱酸する際、従来と同じように
Mを用いて脱酸するものであるが、Mを単独に添加する
ものではなくMとCaO又は、MCab、 CaFzを
結合体、又は混合体として同時に溶鋼へ添加するように
したものである。
That is, in the present invention, when deoxidizing molten steel, M is used to deoxidize as in the conventional method, but instead of adding M alone, a combination of M and CaO, MCab, CaFz, or It is added as a mixture to molten steel at the same time.

Mの添加によって溶鋼中で生成するN2O3は極めて小
さく個々の大きさは数ミクロンなので溶鋼との比重差に
よる自浮力が殆どなく、このため溶鋼中に懸濁分散した
状態となっている。
The N2O3 generated in the molten steel by the addition of M is extremely small, with individual sizes of several microns, so it has almost no self-buoyancy due to the difference in specific gravity with the molten steel, and is therefore suspended and dispersed in the molten steel.

この溶鋼中に懸濁分散しているミクロなAl2O3を浮
上分離させるために前述の種々の対策(バブリング、溶
鋼撹拌、タンデイツシュの堰、 Ar気泡吹込み等)が
実施されているがこれら浮上分離促進型の対策だけでは
溶鋼中に懸濁したM、03を完全に分離するには到って
いない。
In order to float and separate the microscopic Al2O3 suspended and dispersed in this molten steel, the various measures mentioned above (bubbling, stirring of molten steel, tandem weir, Ar bubble injection, etc.) have been implemented. Mold countermeasures alone have not been able to completely separate M and 03 suspended in molten steel.

このAl2O3はタンデイツシュ下部に設置される鋳型
に溶鋼を供給する浸漬ノズル周辺の流量制御機構に付着
して流量制御のバラツキを誘発したり、付着して塊状と
なって欠落し欠陥となったり又、液相と固相の共存する
モールド内の不安定な温度条件と複雑な溶鋼流動の中で
凝集し大型のクラスクーとなりその一部が鋳片に捕捉さ
れると表面疵となったり内部欠陥となることが一般によ
く知られている。
This Al2O3 may adhere to the flow rate control mechanism around the immersion nozzle that supplies molten steel to the mold installed at the bottom of the tundish, causing variations in flow rate control, or may adhere to it and become lumps, causing defects. Under the unstable temperature conditions in the mold where liquid and solid phases coexist and the complex flow of molten steel, it aggregates and forms large cracks, some of which become trapped in the slab, resulting in surface flaws or internal defects. This is generally well known.

本発明はこのミクロ懸濁しているAl2O3を脱酸と同
時にMとの結合体、混合体をなすCaOによりCaO−
/VzOzとせしめることにより表面疵や内部欠陥部に
検出される有害なA7203系介在物とは異なる無害な
形に形態を制御し鋳造工程で付着欠落や凝集捕捉を発生
させない脱酸方法を特徴とするものである。
In the present invention, this micro-suspended Al2O3 is deoxidized and at the same time CaO-
/VzOz to control the morphology to a harmless form different from the harmful A7203 inclusions detected in surface flaws and internal defects, and is characterized by a deoxidizing method that does not cause adhesion failure or agglomeration trapping during the casting process. It is something to do.

即ち、Mを単独で添加すればMは溶鋼中の酸素と反応し
大量のAl2O3を溶鋼中に懸濁させるが、CaOとの
結合体、混合体での添加により生成する脱酸化成物はそ
の組成を同時に添加されたCaOによりCa0−uz0
3となり溶鋼中に懸濁してい<jVzo:+の発生を防
止できる。
That is, if M is added alone, M reacts with oxygen in the molten steel and suspends a large amount of Al2O3 in the molten steel, but the deoxidizing products produced by adding it in combination with CaO or as a mixture Ca0-uz0 due to CaO added at the same time
3, which can prevent the occurrence of <jVzo:+ suspended in the molten steel.

このように形態がCa0−jVz03化した介在物は取
鍋での精錬工程でも合体肥大しやすいため自浮力を持ち
浮上分離しやすく、且、鋳造工程でもタンデイツシュ等
を通過中に浮上分離していく。
Inclusions with a form of Ca0-jVz03 are likely to coalesce and enlarge during the refining process in a ladle, so they have self-buoyancy and are easy to float and separate.In addition, during the casting process, they float and separate while passing through the tundish etc. .

このためモールドまで流出してくるCa0−klz03
は極めて小さいもののみが流出するが、モールド内で浮
上できず鋳片に捕捉される場合でも、CBQ−NzQ3
はモールド内で凝集してクラスター化せず分散捕捉され
ていくので成品欠陥として顕在化することはない。
Therefore, Ca0-klz03 flows out to the mold.
Only extremely small particles flow out, but even if they cannot float in the mold and are captured by the slab, CBQ-NzQ3
Since the particles do not aggregate and form clusters in the mold, but are dispersed and captured, they do not manifest as product defects.

次に本発明の具体的な実施方法について述べる。Next, a concrete implementation method of the present invention will be described.

本発明で脱酸用として用いるjV、 Cab、 CaF
zの結合体、混合体はその脱酸場所、脱酸タイミング等
により操業に適した形状の結合体、混合体とすれば良い
が、その結合体あるいは混合体について第1図、第2図
を用いて説明する。
jV, Cab, CaF used for deoxidation in the present invention
The combination or mixture of I will explain using

第1図は、Mパイプ1の中に、CaO2又はCab。In FIG. 1, an M pipe 1 contains CaO2 or Cab.

CaF、の混合剤2′を充填し、これをカッター3で添
加に適した大きさに切断したAI、 C,llOの結合
体4を示す。もちろん溶鋼中への添加を容易にするため
Mパイプを鉄で被覆してもよい。
A composite body 4 of AI, C, and 11O is shown filled with a mixture 2' of CaF and cut with a cutter 3 into a size suitable for addition. Of course, the M pipe may be coated with iron to facilitate addition to molten steel.

第2図は混合体について説明するものであり、M粉5と
CaO1又はCab、 CaF、混合粉6を混合して混
合体7をつくり、該混合体7は粉状で添加しても良いし
、ある程度のブリケット状に固めて添加しても良い。添
加の場所、タイミングはそれぞれの精錬工程での設備上
の制約や操業上の制約が考えられるので特定は出来ない
が転炉から取鍋への出鋼中の出鋼流に添加してもよいし
、真空脱ガス装置内で添加してもよいし、取鍋でのバブ
リング中の添加、又その他二次精錬での処理中に添加し
てもその効果は変わらない。
FIG. 2 explains a mixture, in which a mixture 7 is made by mixing M powder 5 and CaO1 or Cab, CaF, mixed powder 6, and the mixture 7 may be added in powder form or , it may be added after being hardened into a certain degree of briquette shape. The location and timing of addition cannot be determined because of equipment and operational constraints in each refining process, but it may be added to the tapped stream during tapping from the converter to the ladle. However, the effect remains the same even if it is added in the vacuum degasser, added during bubbling in a ladle, or added during other secondary refining processes.

添加する本発明の複合体の形状は操業実態に合致した操
業性の良い形状、大きさ、混合比率を考慮して決定すれ
ばよい。
The shape of the composite of the present invention to be added may be determined by considering the shape, size, and mixing ratio that provide good operability and match the actual operating conditions.

本発明の溶鋼の脱酸方法を用いるのは、例えば第3図の
如(、吹錬終了後転炉9を傾動し溶鋼10を取鍋IIへ
出鋼する際、AIとCaO1又はMCaO、CaFzの
結合体4を添加しても良いし、第4図の如く、出鋼後に
溶鋼10を不活性ガス12で撹拌しながら結合体4を添
加しても良いし、第5図の如く、溶鋼工0を不活性ガス
12で撹拌しながら、浸漬管13を溶鋼中に浸漬して結
合体4を添加してもよい。また、第6図のように真空脱
ガス槽14内において、結合体4を添加してもよいし、
NとCaO1又はAI、 CaO、CaFzの混合体7
を、不活性ガスと共に直接溶鋼10中に吹き込んでもよ
い。
The method of deoxidizing molten steel of the present invention is used, for example, as shown in FIG. As shown in FIG. 4, the bond 4 may be added while stirring the molten steel 10 with an inert gas 12 after tapping, as shown in FIG. The bonded body 4 may be added by dipping the dip tube 13 into the molten steel while stirring the process 0 with an inert gas 12.Alternatively, as shown in FIG. 4 may be added,
Mixture of N and CaO1 or AI, CaO, CaFz 7
may be directly blown into the molten steel 10 together with an inert gas.

本発明の脱酸方法は前述した以外に、いかなる場所に用
いても良く、用いる場所を特定するものではない。
The deoxidizing method of the present invention may be used at any location other than the one described above, and the location where it is used is not specified.

次に本発明の実施例について述べる。Next, embodiments of the present invention will be described.

(実施例) 実施例(1〕 電縫管用のI’J −S i−キルド鋼についてRHで
の真空処理中にAZ+ Cab、 CaPzの結合体を
用いて脱酸を実施したチャージとMの単独脱酸を実施し
たチャージと介在物の形態比較及び成品でのUST発生
率の比較を行った。その試験結果を以下に示す。
(Example) Example (1) I'J-S i-killed steel for electric resistance welded pipes was deoxidized using a combination of AZ+Cab and CaPz during vacuum treatment at RH.Charge and M alone A comparison was made of the morphology of inclusions and the incidence of UST in the charge that had been deoxidized.The test results are shown below.

試験チャージの成分系と脱酸方法を第1表に、鋼管シー
ム部UST不良率比較(45%斜角深傷。
Table 1 shows the composition of the test charge and the deoxidizing method, and a comparison of the UST defective rate at the seam of steel pipes (45% deep oblique scratches).

80%リジェクト)を第7図に、介在物形態調査結果(
鋳片カットサンプルからの介在物抽出)を第8図に示す
Figure 7 shows the results of the inclusion morphology investigation (80% rejected).
Figure 8 shows the extraction of inclusions from cut slab samples.

実施例〔2] 低炭素A/−キルド鋼について二次精錬での合金添加中
AtのみならびにNとCab、 CaF、の結合体を添
加しその後回−の鋳造、圧延条件を施した板厚0、8 
mmの冷延薄板で製品での「ふくれ」  「スリバー」
の発生率を比較調査した。
Example [2] For low carbon A/-killed steel, only At and a combination of N, Cab, and CaF were added during alloy addition in secondary refining, and subsequent casting and rolling conditions were applied to obtain a plate with a thickness of 0. , 8
``Bulge'' and ``sliver'' in cold-rolled thin sheets of mm
A comparative study was conducted on the incidence of

試験チャージの成分系と脱酸方法を第2表に、成品「ふ
くれ」発生比較(酸洗後の熱延板を目視検査)を第9図
に、成品Uスリバー」発生比較(冷延、焼鈍後の表面を
目視検査)を第10図に示す。
Table 2 shows the component system and deoxidizing method of the test charge, Figure 9 shows a comparison of the occurrence of "blister" in the finished product (visual inspection of the hot rolled sheet after pickling), and comparison of the occurrence of "U sliver" in the finished product (cold rolled, annealed). A visual inspection of the subsequent surface is shown in FIG.

0 第9図、第10図にみられるように純Mの単独脱酸チャ
ージに比較して凝集M2O3に起因する[ふくれJ  
「スリバー」は結合体脱酸を実施することにより低減し
結合体脱酸によるAl2O,の制御効果が確認出来た。
0 As seen in Figs. 9 and 10, compared to the single deoxidizing charge of pure M, the [bulge J
"Sliver" was reduced by deoxidizing the conjugate, and the effect of controlling Al2O by deoxidizing the conjugate was confirmed.

実施例〔3〕 極低炭素AI −T i−キルド鋼についてRHでの脱
炭終了後に混合体を粉状でRHの下部槽から吹き込み、
比較にNの単独脱酸を行ったものと同一条件で連続鋳造
、圧延を行い成品厚み0.75mmの溶融亜鉛成品で「
ふくれ」 「スリバー」の発生率を比較調査した。
Example [3] Regarding ultra-low carbon AI-T i-killed steel, after the decarburization at RH was completed, a mixture was blown in powder form from the lower tank of RH,
For comparison, a molten zinc product with a thickness of 0.75 mm was produced by continuous casting and rolling under the same conditions as those in which N was deoxidized alone.
A comparative study was conducted on the incidence of blister and sliver.

試験チャージの成分系と脱酸方法を第3表に、成品「ふ
くれ」発生比較(酸洗後の熱延板を目視検査)を第11
図に、成品「スリバー」発生比較(冷延、溶融亜鉛メツ
キ後の成品表面を目視検査)を第12図に示す。
The component system and deoxidizing method of the test charge are shown in Table 3, and the comparison of the occurrence of "blister" in the finished product (visual inspection of the hot rolled sheet after pickling) is shown in Table 11.
FIG. 12 shows a comparison of the occurrence of "sliver" in the finished product (visual inspection of the surface of the product after cold rolling and hot-dip galvanizing).

2 第11図、第12図にみられるように純Mの単独脱酸チ
ャージに比較して凝集U、O,に起因する「ふくれ」 
 「スリバー」は混合体のRH下部槽吹き込みにより大
幅に低減し混合体脱酸によるllV2O3の制御効果が
確認出来た。
2 As seen in Figures 11 and 12, "blister" caused by agglomerated U, O, compared to pure M alone deoxidized charge.
"Sliver" was significantly reduced by blowing the mixture into the RH lower tank, and the effect of controlling 11V2O3 by deoxidizing the mixture was confirmed.

尚、本発明に用いる結合体や混合体はNとCa(L又は
/V、 Cab、 CaFzを脱酸剤添加プロセスに合
わせて結合、混合を任意に選択すればよくその組成構成
比率は例えば重量比率で〔第4表〕に示す構成比率のも
のが好ましい。
In addition, the combination or mixture used in the present invention may be arbitrarily selected to combine or mix N and Ca (L or /V, Cab, CaFz) according to the deoxidizing agent addition process. Those having the composition ratios shown in [Table 4] are preferable.

又、添加量は従来のM添加量に対しMが同等量になるよ
うに添加する。この際、脱酸前の溶鋼酸素レベルが高く
生成するlV2O3量が多いものほどCaO比率を高め
るのが効果的である。
Further, the amount of M to be added is the same as that of the conventional amount of M added. At this time, it is more effective to increase the CaO ratio when the molten steel has a higher oxygen level before deoxidation and a larger amount of lV2O3 is generated.

〔第4表〕複合脱酸剤の組成比率例 4 特にCaFzを混入する意味はCaOの滓化を促進させ
効率的なAlzO:+吸着を容易にするものであるが一
般には耐火物の溶損にも影響するので混合量は脱酸剤添
加の方法、温度条件、炉材条件等を勘案し決定すればよ
い。
[Table 4] Composition ratio example 4 of composite deoxidizer 4 The meaning of mixing CaFz in particular is to promote the formation of CaO into slag and facilitate efficient AlzO:+ adsorption, but in general, it causes erosion of refractories. The mixing amount may be determined by taking into consideration the method of adding the deoxidizing agent, temperature conditions, furnace material conditions, etc.

(発明の効果) 本発明によれば溶鋼を脱酸すると同時に成品欠陥の原因
となるミクロN2O3を同時添加のCaOが吸着し成品
でのrUST欠陥」 「ふ(れ」 「スリバー」等の大
幅な低減が可能となりその効果は極めて大きいものであ
る。
(Effects of the Invention) According to the present invention, at the same time as it deoxidizes molten steel, the simultaneously added CaO adsorbs micro-N2O3, which causes product defects, and significantly reduces rUST defects, ``flare'', ``sliver'', etc. in the product. The reduction is possible and the effect is extremely large.

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

第1図は本発明に用いる結合体を示す説明図、第2図は
同じく混合体を示す説明図、第3〜第6図は本発明の脱
酸方法の適用例を示す図、第7図および第8図は実施例
1の試験結果を示す図、第9図および第10図は実施例
2の試験結果を示す図、第11図および第12図は実施
例3の試験結果を示す図である。 5 特開平3 47910 (6) 第7図 第8図 側胴■冊 CaJJ−0系 口=j  klz03系 一] その他組成 第9図 第釦口
FIG. 1 is an explanatory diagram showing a conjugate used in the present invention, FIG. 2 is an explanatory diagram also showing a mixture, FIGS. 3 to 6 are diagrams showing application examples of the deoxidizing method of the present invention, and FIG. 8 shows the test results of Example 1, FIGS. 9 and 10 show the test results of Example 2, and FIGS. 11 and 12 show the test results of Example 3. It is. 5 JP-A-3 47910 (6) Fig. 7 Fig. 8 Side trunk ■ Book CaJJ-0 series opening = j klz03 series 1] Other composition Fig. 9 Button opening

Claims (1)

【特許請求の範囲】[Claims] 未脱酸の溶鋼中へ金属アルミニウム、CaO又は金属ア
ルミニウム、CaO、CaF_2の結合体又は、混合体
を添加し、生成する介在物をCaO−Al_2O_3系
組成とさせて脱酸することを特徴とする溶鋼の脱酸方法
It is characterized by adding metallic aluminum, CaO, or a combination or mixture of metallic aluminum, CaO, and CaF_2 to undeoxidized molten steel, and deoxidizing the generated inclusions by making them have a CaO-Al_2O_3-based composition. Method for deoxidizing molten steel.
JP18046689A 1989-07-14 1989-07-14 Method for deoxidizing molten steel Pending JPH0347910A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18046689A JPH0347910A (en) 1989-07-14 1989-07-14 Method for deoxidizing molten steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18046689A JPH0347910A (en) 1989-07-14 1989-07-14 Method for deoxidizing molten steel

Publications (1)

Publication Number Publication Date
JPH0347910A true JPH0347910A (en) 1991-02-28

Family

ID=16083716

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18046689A Pending JPH0347910A (en) 1989-07-14 1989-07-14 Method for deoxidizing molten steel

Country Status (1)

Country Link
JP (1) JPH0347910A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07189371A (en) * 1993-12-10 1995-07-28 Clestra Hauserman Partition wall system with floating column
JP2002363690A (en) * 2001-06-01 2002-12-18 Daido Steel Co Ltd Steel for plastic molding die
JP2014527581A (en) * 2012-07-19 2014-10-16 中国科学院金属研究所 Method of controlling A segregation of steel ingot by cleaning molten steel

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58141319A (en) * 1982-02-12 1983-08-22 Showa Denko Kk Manufacture of metal refining agent
JPS58141320A (en) * 1982-02-12 1983-08-22 Showa Denko Kk Metal refining agent
JPS5956514A (en) * 1982-09-25 1984-04-02 Nisshin Steel Co Ltd Method for deoxidizing and desulfurizing molten stainless steel

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58141319A (en) * 1982-02-12 1983-08-22 Showa Denko Kk Manufacture of metal refining agent
JPS58141320A (en) * 1982-02-12 1983-08-22 Showa Denko Kk Metal refining agent
JPS5956514A (en) * 1982-09-25 1984-04-02 Nisshin Steel Co Ltd Method for deoxidizing and desulfurizing molten stainless steel

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07189371A (en) * 1993-12-10 1995-07-28 Clestra Hauserman Partition wall system with floating column
JP2002363690A (en) * 2001-06-01 2002-12-18 Daido Steel Co Ltd Steel for plastic molding die
JP4626092B2 (en) * 2001-06-01 2011-02-02 大同特殊鋼株式会社 Steel for plastic molds
JP2014527581A (en) * 2012-07-19 2014-10-16 中国科学院金属研究所 Method of controlling A segregation of steel ingot by cleaning molten steel

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