JPH10102132A - Method of deoxidizing molten steel - Google Patents
Method of deoxidizing molten steelInfo
- Publication number
- JPH10102132A JPH10102132A JP8260676A JP26067696A JPH10102132A JP H10102132 A JPH10102132 A JP H10102132A JP 8260676 A JP8260676 A JP 8260676A JP 26067696 A JP26067696 A JP 26067696A JP H10102132 A JPH10102132 A JP H10102132A
- Authority
- JP
- Japan
- Prior art keywords
- molten steel
- slag
- cao
- sio
- deoxidizing
- 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
Links
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Treatment Of Steel In Its Molten State (AREA)
- Carbon Steel Or Casting Steel Manufacturing (AREA)
Abstract
(57)【要約】
【課題】 低製造原価の原料で従来並の清浄度の高い鋼
を製造するために、スラグ成分調整用に安価な生原料を
利用することを目的としている。
【解決手段】 溶鋼の表面をスラグ成分調整剤で覆った
状態で溶鋼を撹拌して溶鋼を脱酸するに当たり、溶鋼処
理前に成分調整剤として、成分調整用合金からのAlの
インプット量を溶鋼トン当たり5グラム以下、溶鋼処理
終了後のスラグ組成がCaO;35〜60%(重量%、
以下同じ)、SiO2 ;30〜55%、Al2 O3 ;6
〜10%、その他の酸化物生成物の合計を15%以下
で、かつ、CaO/SiO2 ;1.30〜1.70とな
るように、溶鋼処理前に生石灰、シャモット、カルシウ
ムアルミネート及び軟硅石の1種または2種以上と、フ
ッ化ナトリウムあるいはホタル石などのスラグ融点降下
剤を1種あるいは2種以上とを溶鋼に添加し、その後に
溶鋼を撹拌することを特徴とする溶鋼の脱酸方法。(57) [Problem] To provide a low-cost raw material and to produce steel with a high degree of cleanliness as conventionally, an object of the present invention is to use an inexpensive raw material for adjusting slag components. SOLUTION: In stirring molten steel in a state where the surface of the molten steel is covered with a slag component adjusting agent to deoxidize the molten steel, an input amount of Al from a component adjusting alloy is used as a component adjusting agent before the molten steel treatment. 5 g or less per ton, slag composition after molten steel treatment is CaO; 35-60% (% by weight,
Hereinafter the same), SiO 2; 30~55%, Al 2 O 3; 6
10%, in other total of 15% of the oxide product the following, and, CaO / SiO 2; As will be from 1.30 to 1.70, quicklime before the molten steel processing, chamotte, calcium aluminate and soft One or more silica stones and one or more slag melting point depressants such as sodium fluoride or fluorite are added to the molten steel, and thereafter the molten steel is stirred. Acid method.
Description
【0001】[0001]
【発明の属する技術分野】本発明は高炭素鋼線材または
ピアノ線材、SiCr系ばね鋼、オーステナイト系ステ
ンレス鋼ばね材等用の溶鋼を脱酸精練する方法に関する
ものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for deoxidizing and refining molten steel for high-carbon steel wire or piano wire, SiCr spring steel, austenitic stainless steel spring material and the like.
【0002】[0002]
【従来の技術】周知のようにこれらの鋼材では非金属介
在物の形態、大きさが疲労特性やダイス寿命に重大な影
響を及ぼす。また極細線用の高炭素鋼線材においては冷
間加工度が高いために、非金属介在物が冷間加工中の断
線の原因となる。鋼片を熱間圧延および冷間圧延した後
の鋼材中の非金属介在物が微細でしかも圧延方向へ延伸
されていれば悪影響を及ぼさないが、延伸されずに残っ
た粗大な非金属介在物は疲労特性や耐断線性を著しく悪
化させる。この種の非金属介在物としては、種々の組成
のものがあるがAl2 O3 含有量が高い介在物(単体A
l2 O3 やAl2O3 −MgO系介在物)は極めて硬質
で延伸性に欠けるが、Al2 O3 含有量が少なくCaO
−SiO2 −Al2 O3 −MnO系の介在物は延伸性が
極めて良好であり、これらの鋼材を製造においては介在
物を延伸性の良好なものにするための溶鋼脱酸方法が極
めて重要である。2. Description of the Related Art As is well known, in these steel materials, the form and size of nonmetallic inclusions have a significant effect on fatigue characteristics and die life. Further, in a high-carbon steel wire for an ultrafine wire, since the degree of cold working is high, nonmetallic inclusions cause disconnection during cold working. Non-metallic inclusions in the steel material after hot rolling and cold rolling of the slab have no adverse effect if the non-metallic inclusions are fine and stretched in the rolling direction, but coarse non-metallic inclusions remaining without stretching Significantly deteriorates fatigue characteristics and disconnection resistance. As this type of nonmetallic inclusions, there are various compositions, but inclusions having a high Al 2 O 3 content (simple A
l 2 O 3 and Al 2 O 3 -MgO-based inclusions) are extremely hard and lack stretchability, but have a low Al 2 O 3 content and a low CaO content.
-SiO 2 -Al 2 O 3 -MnO-based inclusions are extremely good stretchability, critical molten steel deoxidation method for the favorable stretchability inclusions in producing these steels It is.
【0003】従来これらの鋼材の脱酸方法としてAlの
インプットを5g/ts以下とし、溶鋼表面をCaO含
有スラグで覆い、ガス吹込み用ランスで不活性ガス及び
合成フラックスを吹込み撹拌し、脱酸処理後のスラグ組
成を制御する方法が提案されている。スラグ組成の制御
により非金属介在物の形態制御は可能である。Conventionally, as a method for deoxidizing these steel materials, the input of Al is set to 5 g / ts or less, the surface of molten steel is covered with a slag containing CaO, and an inert gas and a synthetic flux are blown and stirred by a lance for blowing gas. A method for controlling the slag composition after the acid treatment has been proposed. By controlling the slag composition, it is possible to control the form of the nonmetallic inclusions.
【0004】しかしこの方法では硬質な非金属介在物生
成を抑制できるが、スラグ成分調整剤として使用してい
る合成スラグは、原料→粒度、成分調整→焼成(均質
化)→粉砕→粒度の調整、との工程で製造され、高価な
スラグ成分調整剤となっており、これら鋼材が高製造原
価となる主要因であった。However, this method can suppress the formation of hard non-metallic inclusions. However, synthetic slag used as a slag component regulator is obtained by adjusting the raw material → particle size, component adjustment → firing (homogenization) → grinding → particle size. , And are expensive slag component modifiers, and these steel materials were the main factors that resulted in high production costs.
【0005】[0005]
【発明が解決しようとする課題】本発明は以上の事実に
鑑みてなされたもので、低製造原価の原料で従来並の清
浄度の高い鋼を製造するために、スラグ成分調整用に安
価な生原料を利用することを目的としている。SUMMARY OF THE INVENTION The present invention has been made in view of the above facts. In order to produce a steel having a high degree of cleanliness at a low level of production cost and a low level of production cost, it is inexpensive for adjusting slag components. It aims to utilize raw materials.
【0006】[0006]
【課題を解決するための手段】本発明の趣旨は、インジ
ェクション法等による強撹拌条件下では介在物組成はC
aO−SiO2 −Al2 O3 系となるとの知見に基づ
き、スラグ組成の制御により介在物組成を低融点領域に
制御する手法である。スラグ調整剤として高価な焼成処
理済合成スラグを使用せず、安価な生原料を使用しても
滓化剤を適量配合すればインジェクション法による強撹
拌条件下では溶解し、脱酸後スラグ組成制御が可能で、
故に非金属介在物の形態制御を行うことができる。Means for Solving the Problems The gist of the present invention is that the inclusion composition is C under strong stirring conditions such as an injection method.
Based on the finding that the aO-SiO 2 -Al 2 O 3 system, a method of controlling the composition of inclusions to a low melting region by controlling the slag composition. Without using expensive calcined synthetic slag as a slag adjuster, even if inexpensive raw materials are used, if an appropriate amount of a slagging agent is blended, it is dissolved under strong stirring conditions by the injection method, and slag composition control after deoxidation Is possible,
Therefore, morphology control of nonmetallic inclusions can be performed.
【0007】以下、詳細に説明する。The details will be described below.
【0008】介在物組成は溶鋼表面のスラグ組成に強く
影響される。特にCaO/SiO2およびAl2 O3 含
有量に支配され、かつその後の温度低下及び凝固時の2
次脱酸により極めて規則的に組成が変化する。よって、
処理スラグのCaO/SiO2 およびAl2 O3 含有量
を適正な値に制御することにより、介在物の低融点化が
可能である。本発明脱酸方法は溶鋼の表面をCaO含有
スラグで覆った状態で溶鋼を撹拌して脱酸するに当たり
成分調整用合金からのAlのインプット量を溶鋼トン当
たり5グラム以下とする。スラグ成分の調整はCaO含
有量を35〜60%(重量%、以下同じ)、SiO2 含
有量が30〜55%かつCaO含有量とSiO2 含有量
の比CaO/SiO2 が1.30〜1.70となるよう
に調整し、Al2 O3 も6〜10%に調整する。CaO
/SiO2 がこの範囲より低いとSiO2 系の硬質介在
物が生成し鋼材使用時のダイス寿命に影響を及ぼす。こ
の範囲より高いとAl2 O3 、MgO−Al2 O3 系の
硬質介在物が生成し耐断線性を悪化させる。生成介在物
組成を狭範囲に制御するため、その他の酸化物成分の合
計を15%以下とする。スラグ組成が介在物に強く影響
を及ぼすのは溶鋼とスラグの反応に起因するが、反応に
供する時間、つまりスラグ成分調整剤の溶解速度が介在
物組成に影響する。従来法ではスラグ成分調整剤が溶鋼
上に添加されたときに速やかに溶融するよう予め原料の
粒度を調整した上で目標組成にブレンドし、焼成、粉
砕、整粒化し、均質化処理としている。しかしスラグ成
分調整剤の製造原価がこれら鋼材の製造原価に占める割
合は大きく鋼材製造原価低減のため安価な生原料をスラ
グ成分調整剤として使用することとした。生原料は主に
CaO含有量の調整用として生石灰、SiO2 含有量調
整用として軟硅化、Al2O3 含有量調整用としてシャ
モット及びカルシウムアルミネート、滓化促進剤として
ホタル石又はフッ化ナトリウムを使用する。これらを混
合したものをスラグ調整剤とするが、均質化処理及び粒
度調整がなされてないため溶解速度が従来品に比べ著し
く遅くなる。その為、強撹拌条件下でも従来スラグ調整
剤使用時に比べ生成介在物組成は異なることになる。具
体的には溶鋼表面を覆うスラグのCaO含有量とSiO
2 含有量の比CaO/SiO2 を高めに制御し、かつA
l2 O3 含有量も高めに制御することにより生成介在物
組成を低融点領域に制御することが可能となった。生原
料の溶鋼保持容器への挿入はインジェクション処理前に
行わなければならない。[0008] The inclusion composition is strongly influenced by the slag composition on the surface of molten steel. In particular, it is governed by the contents of CaO / SiO 2 and Al 2 O 3 ,
The composition changes very regularly due to secondary deoxidation. Therefore,
By controlling the CaO / SiO 2 and Al 2 O 3 contents of the treated slag to appropriate values, it is possible to lower the melting point of inclusions. In the deoxidation method of the present invention, when the molten steel is stirred and deoxidized while the surface of the molten steel is covered with a slag containing CaO, the input amount of Al from the component adjusting alloy is set to 5 g or less per ton of molten steel. The adjustment CaO content of the slag components 35% to 60% (wt%, hereinafter the same), SiO 2 content of 30 to 55% and CaO content and the ratio CaO / SiO 2 of SiO 2 content 1.30~ Adjust so as to be 1.70, and also adjust Al 2 O 3 to 6 to 10%. CaO
If / SiO 2 is lower than this range, SiO 2 -based hard inclusions are formed and affect the die life when using steel. Above this range the Al 2 O 3, MgO-Al 2 O 3 based hard inclusions exacerbates the generated breakage resistance. In order to control the composition of the formed inclusions in a narrow range, the total of other oxide components is set to 15% or less. Although the slag composition strongly influences the inclusions due to the reaction between the molten steel and the slag, the time for the reaction, that is, the dissolution rate of the slag component modifier, affects the inclusion composition. In the conventional method, the particle size of the raw material is adjusted in advance so that the slag component modifier is quickly melted when added to the molten steel, blended with a target composition, fired, pulverized, sized, and homogenized. However, the production cost of the slag component modifier accounts for a large proportion of the production cost of these steel products, and in order to reduce the production cost of steel products, inexpensive raw materials were used as the slag component modifier. Quicklime for the adjustment of the raw material is mainly CaO content軟硅reduction, chamotte and calcium aluminate as a content of Al 2 O 3 for adjusting, fluorite or sodium fluoride as a slag formation accelerator for the adjustment SiO 2 content Use A mixture of these is used as a slag regulator, but the dissolution rate is significantly slower than that of the conventional product because the homogenization treatment and the particle size adjustment are not performed. Therefore, even under the strong stirring condition, the composition of the formed inclusion is different from that of the conventional slag conditioner. Specifically, the CaO content of the slag covering the molten steel surface and the SiO2
2 The content ratio CaO / SiO 2 is controlled to be relatively high, and A
By controlling the l 2 O 3 content to be relatively high, the composition of the formed inclusions can be controlled in the low melting point region. The raw material must be inserted into the molten steel holding container before the injection treatment.
【0009】尚、生原料の添加方法は、極力、早期に溶
解するように出鋼完了後の溶鋼上に添加するよりは、出
鋼前に鍋内に入れ置くか、あるいは、出鋼中に添加する
のが望ましい。In addition, the raw material is added in a pot before tapping or during tapping, rather than on the molten steel after tapping is completed so as to melt as early as possible. It is desirable to add.
【0010】[0010]
【発明の実施の形態】強撹拌条件の取鍋処理においてス
ラグ組成調整剤として、均質度は劣るが安価である生原
料を使用しても、従来材並の非金属介在物組成制御精度
を有するものである。BEST MODE FOR CARRYING OUT THE INVENTION In a ladle treatment under a strong stirring condition, even if a raw material having a low homogeneity but an inexpensive raw material is used as a slag composition adjuster, the composition control accuracy of nonmetallic inclusions is equal to that of conventional materials. Things.
【0011】[0011]
【実施例】溶鋼240tonを取鍋に出鋼時、成分調整
としてFeMn2.9kg/ts、Al含有量が0.0
3%以下のFeSiを投入し表1に記載した処理前成分
となった。表2の配合比の生原料(品位は表3)を出鋼
完了後溶鋼表面上に投入した。取鍋内溶鋼処理に際して
ランスから吹込みガスとともにCaO−CaF2 を主成
分とする粉体を吹込み、その後Arガスを1.0Nm3
/min吹込み30分処理しスラグを激しく撹拌した。
得られた溶鋼をタンディッシュに空気酸化防止用のロン
グノズルを介して注入し、更に浸漬ノズルを介して断面
サイズ300mm×500mmの連続鋳造用鋳型に注入
し凝固させた。本実施例の溶鋼の処理後の成分及び最終
スラグ成分をそれぞれ表1および表4に示す。最終スラ
グ成分は本発明の範囲内であることは明らかである。更
に得られたブルーム鋳片を1300℃に加熱し120m
m×120mmのビレットに熱間圧延し、冷却後更に1
100℃に加熱し直径5.5mmの線材に熱間圧延し、
圧延鋼材中の非金属介在物を調査した。結果を図1に示
す。図示の如く非延性介在物指数も従来材と同程度で硬
質介在物の発生は抑制されていた。EXAMPLE When molten steel 240 ton was put into a ladle, FeMn was 2.9 kg / ts and the Al content was 0.0
3% or less of FeSi was added to obtain the components before treatment described in Table 1. Raw materials having the compounding ratios shown in Table 2 (grade 3 in Table 3) were put on the molten steel surface after tapping was completed. At the time of molten steel treatment in the ladle, a powder mainly composed of CaO-CaF 2 is blown from a lance together with a blow gas, and then Ar gas is blown to 1.0 Nm 3.
/ Min was blown for 30 minutes and the slag was vigorously stirred.
The obtained molten steel was injected into a tundish through a long nozzle for preventing air oxidation, and further injected through an immersion nozzle into a continuous casting mold having a cross section of 300 mm x 500 mm to solidify. Tables 1 and 4 show the components after treatment and the final slag components of the molten steel of this example. It is clear that the final slag component is within the scope of the present invention. Further, the obtained bloom slab was heated to 1300 ° C.
hot rolled into a billet of mx 120 mm, and after cooling,
Heated to 100 ° C and hot rolled into a 5.5mm diameter wire rod,
Nonmetallic inclusions in rolled steel were investigated. The results are shown in FIG. As shown in the figure, the index of non-ductile inclusions was about the same as that of the conventional material, and the generation of hard inclusions was suppressed.
【0012】<比較例1>生原料を表2の配合とし実施
例と同じ要領で成分調整用の合金および生原料を添加し
た。取鍋内溶鋼処理、及び非金属介在物調査方法も実施
例と同様に行った。表4に最終スラグ成分、図1に非延
性介在物指数の調査結果を示す。本スラグ組成ではSi
O2 系介在物が多量に生成している。<Comparative Example 1> Raw materials were blended as shown in Table 2 and alloys for component adjustment and raw materials were added in the same manner as in Examples. The molten steel treatment in the ladle and the method of investigating nonmetallic inclusions were performed in the same manner as in the example. Table 4 shows the final slag components, and FIG. 1 shows the results of investigation of the non-ductile inclusion index. In this slag composition, Si
O 2 -based inclusions are generated in large quantities.
【0013】<比較例2>生原料を表2の配合とし実施
例と同じ要領で成分調整用の合金および生原料を添加し
た。取鍋内溶鋼処理、及び非金属介在物調査方法も実施
例と同様に行った。表4に最終スラグ成分、図1に非延
性介在物指数の調査結果を示す。本スラグ組成ではAl
2 O3 系介在物が多量に生成している。<Comparative Example 2> The raw materials were blended as shown in Table 2 and alloys and raw materials for component adjustment were added in the same manner as in the examples. The molten steel treatment in the ladle and the method of investigating nonmetallic inclusions were performed in the same manner as in the example. Table 4 shows the final slag components, and FIG. 1 shows the results of investigation of the non-ductile inclusion index. In this slag composition, Al
A large amount of 2 O 3 -based inclusions is generated.
【0014】[0014]
【表1】 [Table 1]
【0015】[0015]
【表2】 [Table 2]
【0016】[0016]
【表3】 [Table 3]
【0017】[0017]
【表4】 [Table 4]
【0018】[0018]
【発明の効果】本発明により図2に示す如く安価製造コ
ストで、かつ従来レベルの非金属介在物制御精度を有す
る製造プロセスを開発した。According to the present invention, a manufacturing process having a low manufacturing cost and a conventional level of nonmetallic inclusion control accuracy has been developed as shown in FIG.
【図面の簡単な説明】[Brief description of the drawings]
【図1】非延性介在物指数における従来材と本発明材及
び比較例との比較した図。FIG. 1 is a diagram comparing a conventional material with a material of the present invention and a comparative example in a non-ductile inclusion index.
【図2】スラグ調整材原単価における従来材と本発明材
との比較図。FIG. 2 is a comparison diagram of a conventional material and a material of the present invention at a slag adjusting material original unit price.
Claims (3)
状態で溶鋼を撹拌して溶鋼を脱酸するに当たり、 成分調整用合金からのAlのインプット量を溶鋼トン当
たり5グラム以下とし、 溶鋼処理終了後のスラグ組成がCaO;35〜60%
(重量%、以下同じ)、SiO2 ;30〜55%、Al
2 O3 ;6〜10%、その他の酸化物生成物の合計を1
5%以下で、かつ、CaO/SiO2 ;1.30〜1.
70となるように、溶鋼処理前に生石灰、シャモット、
カルシウムアルミネート及び軟硅石の1種または2種以
上と、フッ化ナトリウムあるいはホタル石などのスラグ
融点降下剤を1種あるいは2種以上とを溶鋼に添加し、 その後に溶鋼を撹拌することを特徴とする溶鋼の脱酸方
法。1. A method for mixing molten steel in a state where the surface of the molten steel is covered with a slag component modifier and deoxidizing the molten steel, wherein an input amount of Al from the alloy for component adjustment is 5 g or less per ton of molten steel. Slag composition after treatment is CaO; 35-60%
(% By weight, hereinafter the same), SiO 2 ; 30 to 55%, Al
2 O 3 ; 6 to 10%, total of other oxide products is 1
5% or less, and, CaO / SiO 2; 1.30~1.
70, so that quicklime, chamotte,
One or more of calcium aluminate and soft silica and one or more of slag melting point depressant such as sodium fluoride or fluorite are added to molten steel, and then the molten steel is stirred. Method of deoxidizing molten steel.
て、 生石灰、シャモット、カルシウムアルミネート及び軟硅
石の1種または2種以上と、フッ化ナトリウムあるいは
ホタル石などのスラグ融点降下剤を1種あるいは2種以
上とを、 転炉からの出鋼前に鍋内に添加する、あるいは、出鋼中
に添加することを特徴とする溶鋼の脱酸方法。2. The method for deoxidizing molten steel according to claim 1, wherein one or more of quick lime, chamotte, calcium aluminate, and soft silica are combined with a slag melting point depressant such as sodium fluoride or fluorite. A method for deoxidizing molten steel, comprising adding a seed or two or more kinds to a pot before tapping from a converter or during tapping.
脱酸方法において、溶鋼の撹拌をインジェクションラン
スにより不活性ガスを吹込み溶鋼を撹拌することを特徴
とする溶鋼の脱酸方法。3. The method for deoxidizing molten steel according to claim 1, wherein the molten steel is stirred by blowing an inert gas with an injection lance to agitate the molten steel.
Priority Applications (1)
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JP26067696A JP3766478B2 (en) | 1996-10-01 | 1996-10-01 | Deoxidation method for molten steel |
Applications Claiming Priority (1)
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JP26067696A JP3766478B2 (en) | 1996-10-01 | 1996-10-01 | Deoxidation method for molten steel |
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JPH10102132A true JPH10102132A (en) | 1998-04-21 |
JP3766478B2 JP3766478B2 (en) | 2006-04-12 |
Family
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JP26067696A Expired - Fee Related JP3766478B2 (en) | 1996-10-01 | 1996-10-01 | Deoxidation method for molten steel |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002332517A (en) * | 2001-05-11 | 2002-11-22 | Nippon Steel Corp | Manufacturing method of high carbon steel wire |
JP2007092164A (en) * | 2005-09-05 | 2007-04-12 | Kobe Steel Ltd | Steel wire rod having excellent drawability and fatigue properties, and manufacturing method of the same |
JP2008150683A (en) * | 2006-12-19 | 2008-07-03 | Kobe Steel Ltd | Method for manufacturing steel wire rod excellent in fatigue characteristic |
CN110052473A (en) * | 2019-04-16 | 2019-07-26 | 北京净界新宇环保科技有限公司 | A kind of heavy metal chromium pollution processing method |
-
1996
- 1996-10-01 JP JP26067696A patent/JP3766478B2/en not_active Expired - Fee Related
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002332517A (en) * | 2001-05-11 | 2002-11-22 | Nippon Steel Corp | Manufacturing method of high carbon steel wire |
JP2007092164A (en) * | 2005-09-05 | 2007-04-12 | Kobe Steel Ltd | Steel wire rod having excellent drawability and fatigue properties, and manufacturing method of the same |
JP4718359B2 (en) * | 2005-09-05 | 2011-07-06 | 株式会社神戸製鋼所 | Steel wire rod excellent in drawability and fatigue characteristics and manufacturing method thereof |
US8668783B2 (en) | 2005-09-05 | 2014-03-11 | Kobe Steel, Ltd. | Steel wire rod having excellent drawability and fatigue properties, and manufacturing method of the same |
JP2008150683A (en) * | 2006-12-19 | 2008-07-03 | Kobe Steel Ltd | Method for manufacturing steel wire rod excellent in fatigue characteristic |
CN110052473A (en) * | 2019-04-16 | 2019-07-26 | 北京净界新宇环保科技有限公司 | A kind of heavy metal chromium pollution processing method |
Also Published As
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JP3766478B2 (en) | 2006-04-12 |
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