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JPS6315060B2 - - Google Patents
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JPS6315060B2 - - Google Patents

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Publication number
JPS6315060B2
JPS6315060B2 JP57215488A JP21548882A JPS6315060B2 JP S6315060 B2 JPS6315060 B2 JP S6315060B2 JP 57215488 A JP57215488 A JP 57215488A JP 21548882 A JP21548882 A JP 21548882A JP S6315060 B2 JPS6315060 B2 JP S6315060B2
Authority
JP
Japan
Prior art keywords
flux
inclusions
amount
mold
viscosity
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
JP57215488A
Other languages
Japanese (ja)
Other versions
JPS59107754A (en
Inventor
Taketo Nakano
Tadao Kishi
Kunio Koyama
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 JP21548882A priority Critical patent/JPS59107754A/en
Publication of JPS59107754A publication Critical patent/JPS59107754A/en
Publication of JPS6315060B2 publication Critical patent/JPS6315060B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D11/00Continuous casting of metals, i.e. casting in indefinite lengths
    • B22D11/10Supplying or treating molten metal
    • B22D11/11Treating the molten metal

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Continuous Casting (AREA)

Description

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

本発明は、アルミキルド鋼の連続鋳造方法に関
するものである。 鋼の連続鋳造は、省エネルギー、省工程の達成
のため近年急速に発達した。しかし更に連続鋳造
から連続圧延と一貫した合理的な鋼の製造技術の
確立や更に高品質の鋳片を製造するためには、な
お一層優れた連続鋳造技術を確立する必要があ
る。 特に自動車用鋼板等に広く用いられるアルミキ
ルド鋼において、Al2O3介在物を低減させ、鋳造
後無手入れで圧延しても製品のスリバー疵や深絞
り加工時に割れ発生のない鋳造方法を開発するこ
とは、高品質成品の確保や省工程によるコストダ
ウン等の点から近年ますますその必要性が大とな
つた。 即ち、アルミキルド鋼は、製鋼工程において、
鋼中の余剰酸素を除去するため、Al、Fe−Al合
金、Al−Si合金、Al−Mg合金などのAlを含有し
た物質を使用した鋼を言い、このアルミキルド鋼
においては、当然Al2O3を主体とする酸化物即ち
Al2O3系介在物が形成される。 連続鋳造の鋳型内の介在物は、鋳型に入る前工
程まででは除去されず鋳型内に流入するもの、又
溶鋼が鋳型内に流入するとき酸素と接触し、その
時新たに生成するものなどがある。この鋳型に流
入した介在物は、溶鋼の流れに乗つて流動する。
そして溶鋼と介在物の比重差、あるいは溶鋼を鋳
型内に流入させるときの酸性防止用シールドガス
のバブリング等によつて溶鋼中の介在物の一部が
溶鋼表面に浮上する。そして浮上した介在物の一
部が鋳型内の溶融したフラツクスと反応し、吸収
され排出される。しかし溶鋼表面に浮上しても溶
融したフラツクスと反応せず、再び溶鋼の流れに
乗つて溶鋼中に捲込まれるものもある。 そして鋼が凝固する時、当然その中にある介在
物は固定される。 この鋼中に固定された介在物の分布を観察する
と鋳片表面層に多く偏在している。これが鋳片を
圧延したときのスリバー疵の原因、あるいは深絞
り加工をしたときの割れの原因となる。 このためアルミキルド鋼の良好な鋳片を鋳造す
るためには、Al2O3介在物の浮上を促進し、そし
て浮上した介在物が再び溶鋼中に捲込まれないよ
うに除去することが必要である。 鋳型内の介在物の浮上挙動は前述したように溶
鋼流や、シールドガスのバブリング等によつて影
響される。このため介在物の浮上促進には、溶鋼
流の適正化や、シールドガス流の適正化が必要で
ある。又浮上した介在物をより多く除去するため
には、フラツクス組成の適正化が必要である。 更に連続鋳造において良好な鋳片を得るために
は、フラツクスが鋳型と鋳片の間に流入し、鋳型
と鋳片の間の潤滑剤として又伝熱媒体としての適
正な性能が要求される。このためには鋳型と鋳片
の間にフラツクスを均一に流入させなければなら
ない。したがつて、均一な流入を確保するために
は、鋳造条件、特に鋳片引抜速度に応じてのフラ
ツクスの適正粘度の確保が必要である。又、フラ
ツクスは前述したように溶鋼からの介在物を吸収
し、排出する性能が要求されるが、この介在物と
反応したとき粘度の変化等が予想される。この粘
度変化は、流入挙動に著しく影響するため粘度変
化を軽減させ、且つその変化量を許容量内に抑え
る必要がある。 本発明は、アルミキルド鋼のAl2O3介在物の鋳
型内での浮上挙動と浮上した介在物の溶融したフ
ラツクスと反応し排出される挙動を詳細に研究実
験し、これら挙動を定量的に解析した結果、なさ
れたものであつて、その要旨とするところは、ア
ルミキルド鋼の連続鋳造において、不活性ガスを
鋳型単位断面積(m2)あたり20/min〜130
/minの範囲で溶鋼に吹込み、且つ浸漬ノズル
の溶鋼吐出口の中心が溶鋼表面から120mm〜220mm
の範囲で浸漬し、鋳型内添加フラツクスを(1)式に
よつて求めた塩基度Bを1.3以上に規制して、
Al2O3介在物を鋳型単位断面積(m2)あたり30
g/min以上溶鋼中より排出し、且つその排出さ
れたAl2O3介在物を吸収した鋳型内溶融フラツク
スの粘度ηx(Poise)を(2)式によつて求め、それ
が鋳片引抜速度に応じて(3)式で求められる範囲に
なるよう規制して鋳造することを特徴とするアル
ミキルド鋼の連続鋳造法にある。 B=1.53・CaO+1.51・MgO+1.37・K2O+1.94・Na2O+1
.53・CaF2+3.55・Li2O+3.27・NaF/1.48・SiO2+0.36
・TiO2+0.10・Al2O3 ……(1) 但し、各成分は重量(%) ηx=(0.55+0.34×1.12x)/(0.55+0.34×1.12
x0)η(2) 但し、η:Al2O3吸収前のフラツクスの1300℃
における粘度(Poise) x0:フラツクスがもともと含有しているAl2O3
(%) x:Al2O3介在物を吸収した溶融フラツクス中の
Al2O3(%) 1.0/V≦ηx≦4.0/V (3) 但し、V:鋳片の引抜速度(m/min) 以下本発明について詳細に説明する。 まずここで言うシールドガスとはAr・N2又は
He等の従来からシールド用ガスとして使用され
ている不活性ガスを指すものである。 この吹込み量は、鋳型内に溶鋼を注入するとき
の浸漬ノズル内の酸化防止材としての考え方から
溶鋼の注入速度、又は浸漬ノズルの断面積等の函
数として通常考えられているが、本発明において
不活性ガスを鋳型単位断面積(m2)あたりのガス
吹込み量(/min)で規制した。これはガス吹
込みは鋳型内溶鋼中でのバブリング現象であり、
Al2O3介在物の浮上にも大きく寄与しているとの
見地から、鋳型内でのバブリングの頻度を表わす
と考えられる前記断面積あたりのガス吹込み量
で、規制したものである。なお、この吹込み量は
浸漬ノズルの中を通過した量であり、浸漬ノズル
継ぎ面の周囲のシールド用に流し、浸漬ノズル内
に流入せずそのまま排出されたものは含まれな
い。その下限を1m2あたり20/minとしたのは
20/min未満ではAl2O3介在物の排出が不充分
でスリバー疵の発生が防止できないためである。
一方吹込み量が130/minを超えるとAl2O3介在
物の排出は充分であるが、ガスの吹込み量過大に
よる過剰のバブリングになり、スラグ捲込みを生
じ、これがスリバー疵の原因となるため避けなけ
ればならない。このような理由により吹込み量の
上限を130/minに規定した。なお後述の実施
例にも示す如く不活性ガスをまつたく吹込まない
場合にもAl2O3の排出は行なわれるが、この場合
溶鋼が浸漬ノズル内を通過する間に酸化され、こ
れによつて生じたAl2O3介在物が鋳型内に多く捲
込まれるためスリバー疵などの発生が多くなる。 次に浸漬ノズルの溶鋼吐出口の中心が溶鋼表面
から120mm〜220mmの位置に来るように浸漬するの
は次の理由によるものである。 まず浸漬深さが120mm未満では、Al2O3介在物
の排出量は大きいが、溶鋼の湯面変動のためと考
えられるスラグ捲込み、スリバー疵が発生する。
一方浸漬深さ220mm超では溶鋼表面温度が低くな
り過ぎる傾向がみられ、Al2O3介在物の排出量も
小さく鋳片の表面割れ、スラグ捲込み、スリバー
疵などの発生がみられる。以上の理由により、浸
漬ノズルの浸漬深さを120mm〜220mmと規定した。 次にフラツクスの塩基度の規定について述べ
る。 鋳型内に添加するフラツクスの塩基度が高くな
る程フラツクスによるAl2O3の吸収量は大きくな
る。この場合、本発明においてのフラツクスの塩
基度は、次式(1)で表わすものであり、塩基度Bが
1.3以上であることを必要とする。Bが1.3未満で
あると、鋳片表面に割れが発生するので実用に供
し得ない。 なおBの式(1)はまずSiO2・CaO等の各成分の
イオン−酸素間引力Iを求め、そして1.56を中立
点として各成分のIより差引き、この値を各成分
のモル%を重量%に換算するため、各成分の分子
量での商を求め、なお係数を簡略化するため100
倍し、そして負の値の係数の成分の和を分子に正
の値の係数の成分の和を分母とし、その商をBと
したものである。例えばSiO2のイオン−酸素間
引力Iは2.45で、これより1.56を引くと0.89これ
をSiO2の分子量60で割ると0.0148これに100を掛
けSiO2の係数とし、正の値をとるため分母とし
た。弗化物についても同様の考え方で係数を求め
た。 B=1.53・CaO+1.51MgO+1.37・K2O+1.94・Na2O+1.5
3・CaF2+3.55・Li2O+3.27・NaF/1.48・SiO2+0.36・
TiO2+0.10・Al2O3 ……(1) 但し、各成分は重量(%)。 このように本発明において用いるフラツクス
は、Bが1.3以上であれば特にその組成を限定す
るものではない。さらにフラツクスの形態も又特
に限定するものではないが、原材料を配合混合、
この混合物を溶解粉砕、これに溶融調整剤と造粒
剤を加え造粒乾燥したものが最も好ましい。 この場合原材料としては、石灰石、硅灰石、硅
砂、ソーダ灰、炭酸リチウム、蛍石、弗化ソー
ダ、アルミナ、マグネシア等が適当な組合わせで
使用する。 望ましい成分範囲としては、SiO220〜45%、
Al2O30〜15%、CaO20〜45%、MgO0〜20%、
CaF2+NaF5〜30%、Na2O+K2O+Li2O5〜29
%、C0.4〜7%その他必要に応じて、あるいは使
用原材料の不純物として、FeO・MnO・TiO2
BaO等を合計0.5〜10%程度含有することもでき
る。なおこの場合、後述するようにフラツクスに
もともと含まれるAl2O3の量はなるべく低目に抑
えておくことが望ましい。 次にAl2O3介在物の溶鋼からの排出量を鋳型単
位断面積(m2)あたり30g/min以上としたの
は、排出が30g/min未満では鋳片表面層の残留
介在物が多く圧延加工したときのスリバー疵、あ
るいは深絞り加工したときの割れ発生等の欠陥が
発生するためである。なおこの排出量は次のよう
にして求めることができる。即ち、鋳型内に添加
し、鋳型と鋳片の間に流し、鋳型下端から排出す
るフラツクスをサンプリングし、そしてこれに含
まれるAl2O3量を測定し、これからフラツクスが
もともと含有していたAl2O3量を差引き、これに
時間あたり排出されたフラツクス量を掛けること
によつて排出量を求め、更にこの排出された
Al2O3量を鋳型内断面積で割ることによつて鋳型
単位断面積あたりの排出量が求められるものであ
り、又これによつて鋳型サイズの相違による差を
補正することが可能である。 このようにシールドガス吹込み量、浸漬ノズル
の浸漬深さ、又使用するフラツクスの塩基度で溶
鋼中のAl2O3介在物の排出量を制御できるもので
あり、これらそれぞれの最適条件の組合わせで最
大のAl2O3介在物の排出ができる。 しかし従来の先行技術、例えば特開昭52−
26318号等に示されているように更に鋳片引抜速
度に応じて、溶融フラツクスの粘度を規制する必
要がある。このためまず溶融フラツクスがAl2O3
介在物を吸収して粘度がどのように変化するかを
検討した。その結果を第1図に示す。
The present invention relates to a continuous casting method for aluminum killed steel. Continuous casting of steel has developed rapidly in recent years to achieve energy savings and process savings. However, in order to establish a rational steel manufacturing technology that is consistent with continuous casting and continuous rolling, and to manufacture slabs of even higher quality, it is necessary to establish an even better continuous casting technology. In particular, we will develop a casting method that reduces Al 2 O 3 inclusions in aluminum-killed steel, which is widely used in automobile steel plates, etc., and will not cause sliver defects or cracks during deep drawing even when rolled without maintenance after casting. This has become increasingly necessary in recent years from the standpoint of ensuring high-quality products and reducing costs through process-saving steps. In other words, in the steelmaking process, aluminum killed steel is
In order to remove excess oxygen in steel, it refers to steel that uses materials containing Al, such as Al, Fe-Al alloy, Al-Si alloy, Al-Mg alloy, etc. In this aluminum killed steel, naturally Al 2 O 3 -based oxides, i.e.
Al 2 O 3 based inclusions are formed. Inclusions in continuous casting molds include those that are not removed before entering the mold and flow into the mold, and those that are newly formed when molten steel comes into contact with oxygen when it flows into the mold. . The inclusions that have flowed into the mold flow along with the flow of molten steel.
Then, some of the inclusions in the molten steel float to the surface of the molten steel due to the difference in specific gravity between the molten steel and the inclusions, or due to bubbling of an acid-preventing shielding gas when the molten steel flows into the mold. A portion of the floating inclusions reacts with the molten flux in the mold, is absorbed, and is discharged. However, even if they float to the surface of the molten steel, some of them do not react with the molten flux and are once again caught up in the flow of the molten steel. When the steel solidifies, the inclusions within it are naturally fixed. When observing the distribution of inclusions fixed in this steel, many of them are unevenly distributed on the surface layer of the slab. This causes sliver defects when the slab is rolled or cracks when deep drawing is performed. Therefore, in order to cast a good slab of aluminium-killed steel, it is necessary to promote the floating of Al 2 O 3 inclusions and to remove the floated inclusions to prevent them from being drawn into the molten steel again. be. As mentioned above, the floating behavior of inclusions in the mold is influenced by the flow of molten steel, bubbling of shielding gas, and the like. Therefore, to promote the floating of inclusions, it is necessary to optimize the flow of molten steel and the flow of shielding gas. Furthermore, in order to remove more floating inclusions, it is necessary to optimize the flux composition. Furthermore, in order to obtain a good slab in continuous casting, flux flows between the mold and the slab, and is required to have appropriate performance as a lubricant between the mold and the slab and as a heat transfer medium. For this purpose, the flux must flow uniformly between the mold and the slab. Therefore, in order to ensure uniform inflow, it is necessary to ensure an appropriate viscosity of the flux depending on the casting conditions, especially the slab drawing speed. Further, as mentioned above, flux is required to have the ability to absorb and discharge inclusions from molten steel, and when it reacts with these inclusions, changes in viscosity, etc. are expected. Since this viscosity change significantly affects the inflow behavior, it is necessary to reduce the viscosity change and suppress the amount of change within an allowable amount. The present invention involves conducting detailed research experiments on the floating behavior of Al 2 O 3 inclusions in aluminum killed steel in a mold and the behavior of the floating inclusions reacting with molten flux and being ejected, and quantitatively analyzing these behaviors. As a result of this research, the gist is that in continuous casting of aluminum-killed steel, inert gas is applied at a rate of 20/min to 130/min per mold unit cross-sectional area (m 2 ).
/min into the molten steel, and the center of the molten steel discharge port of the immersion nozzle is 120 mm to 220 mm from the molten steel surface.
The flux added in the mold is regulated to a basicity B of 1.3 or more, which is determined by equation (1).
30 Al 2 O 3 inclusions per mold unit cross-sectional area (m 2 )
The viscosity ηx (Poise) of the in-mold molten flux discharged from the molten steel and absorbing the discharged Al 2 O 3 inclusions is determined by equation (2), and it is determined by the slab drawing speed. A continuous casting method for aluminum killed steel is characterized in that casting is controlled within the range determined by equation (3) according to the following conditions. B=1.53・CaO+1.51・MgO+1.37・K2O +1.94・Na2O +1
.53・CaF 2 +3.55・Li 2 O+3.27・NaF/1.48・SiO 2 +0.36
・TiO 2 +0.10・Al 2 O 3 ...(1) However, each component is weight (%) η x = (0.55 + 0.34 x 1.12 x ) / (0.55 + 0.34 x 1.12
x0 )η(2) However, η: 1300℃ of flux before Al 2 O 3 absorption
Viscosity (Poise) x 0 : Al 2 O 3 originally contained in the flux
(%) x: In the molten flux that absorbed Al 2 O 3 inclusions
Al 2 O 3 (%) 1.0/V≦η x ≦4.0/V (3) where V: drawing speed of slab (m/min) The present invention will be described in detail below. First of all, the shielding gas mentioned here is Ar・N2 or
This refers to inert gases such as He, which have traditionally been used as shielding gases. This amount of injection is usually considered as a function of the molten steel injection speed or the cross-sectional area of the immersion nozzle, etc., since it is used as an antioxidant in the immersion nozzle when molten steel is injected into the mold. Inert gas was regulated by the amount of gas blown into the mold (/min) per unit cross-sectional area (m 2 ) of the mold. This is because gas injection is a bubbling phenomenon in the molten steel in the mold.
From the viewpoint that it greatly contributes to the floating of Al 2 O 3 inclusions, the amount of gas blown per cross-sectional area is regulated, which is considered to represent the frequency of bubbling within the mold. Note that this blown amount is the amount that passed through the immersion nozzle, and does not include the amount that was flowed for shielding around the joint surface of the immersion nozzle and was discharged as is without flowing into the immersion nozzle. The lower limit was set at 20/min per 1m2 .
This is because if the speed is less than 20/min, the discharge of Al 2 O 3 inclusions will be insufficient and the occurrence of sliver defects cannot be prevented.
On the other hand, if the blowing rate exceeds 130/min, the Al 2 O 3 inclusions can be sufficiently discharged, but excessive bubbling occurs due to the excessive gas blowing rate, causing slag entrainment, which is the cause of sliver defects. must be avoided. For this reason, the upper limit of the blowing rate was set at 130/min. As shown in the examples below, Al 2 O 3 can be discharged even when inert gas is not blown in, but in this case, the molten steel is oxidized while passing through the immersion nozzle, and as a result, Al 2 O 3 is discharged. As a result, many Al 2 O 3 inclusions are rolled into the mold, which increases the occurrence of sliver defects. Next, the reason why the molten steel is immersed so that the center of the molten steel discharge port of the immersion nozzle is located at a position of 120 mm to 220 mm from the molten steel surface is as follows. First, when the immersion depth is less than 120 mm, the amount of Al 2 O 3 inclusions discharged is large, but slag entrainment and sliver defects occur, which are thought to be due to fluctuations in the molten steel level.
On the other hand, when the immersion depth exceeds 220 mm, the surface temperature of the molten steel tends to become too low, and the amount of Al 2 O 3 inclusions discharged is small, causing surface cracks in the slab, slag entrainment, sliver defects, etc. For the above reasons, the immersion depth of the immersion nozzle was defined as 120 mm to 220 mm. Next, we will discuss the regulation of basicity of flux. The higher the basicity of the flux added into the mold, the greater the amount of Al 2 O 3 absorbed by the flux. In this case, the basicity of the flux in the present invention is expressed by the following formula (1), and the basicity B is
Requires 1.3 or higher. If B is less than 1.3, cracks will occur on the surface of the slab and it cannot be put to practical use. In equation (1) for B, first find the ion-oxygen attraction force I of each component such as SiO 2 and CaO, then subtract it from the I of each component using 1.56 as the neutral point, and use this value to calculate the mole% of each component. In order to convert to weight%, calculate the quotient of the molecular weight of each component, and to simplify the coefficient, 100
The numerator is the sum of the coefficient components with negative values, the denominator is the sum of the coefficient components with positive values, and the quotient is B. For example, the ion-oxygen attraction I of SiO 2 is 2.45, subtracting 1.56 from this gives 0.89, dividing this by the molecular weight of SiO 2 60, 0.0148, multiplying this by 100 to get the coefficient of SiO 2 , and since it takes a positive value, the denominator And so. The coefficient was calculated for fluoride using the same concept. B=1.53・CaO+1.51MgO+1.37・K2O +1.94・Na2O +1.5
3・CaF 2 +3.55・Li 2 O+3.27・NaF/1.48・SiO 2 +0.36・
TiO 2 +0.10・Al 2 O 3 ...(1) However, each component is by weight (%). As described above, the composition of the flux used in the present invention is not particularly limited as long as B is 1.3 or more. Furthermore, the form of the flux is not particularly limited, but may include mixing raw materials,
Most preferably, this mixture is melted and pulverized, a melt modifier and a granulating agent are added thereto, and the mixture is granulated and dried. In this case, as raw materials, limestone, wollastonite, silica sand, soda ash, lithium carbonate, fluorite, sodium fluoride, alumina, magnesia, etc. are used in an appropriate combination. Desirable component ranges include SiO 2 20-45%;
Al2O3 0 ~15%, CaO20~45%, MgO0~20%,
CaF2 +NaF5~30%, Na2O + K2O + Li2O5 ~29
%, C0.4-7%, FeO, MnO, TiO 2 , etc. as necessary or as impurities in the raw materials used.
It is also possible to contain BaO and the like in a total amount of about 0.5 to 10%. In this case, as will be described later, it is desirable to keep the amount of Al 2 O 3 originally contained in the flux as low as possible. Next, we set the amount of Al 2 O 3 inclusions discharged from molten steel to 30 g/min or more per mold unit cross-sectional area (m 2 ) because if the discharge is less than 30 g/min, there are many inclusions remaining on the surface layer of the slab. This is because defects such as sliver flaws occur during rolling or cracks occur during deep drawing. Note that this emission amount can be determined as follows. That is, the flux added into the mold, flowed between the mold and the slab, and discharged from the bottom end of the mold was sampled, and the amount of Al 2 O 3 contained in this was measured. Determine the amount of emissions by subtracting the amount of 2 O 3 and multiplying it by the amount of flux emitted per hour, and then calculate the amount of flux emitted per hour.
By dividing the amount of Al 2 O 3 by the internal cross-sectional area of the mold, the amount of discharge per unit cross-sectional area of the mold can be determined, and it is also possible to correct the difference due to the difference in mold size. . In this way, the amount of Al 2 O 3 inclusions discharged from molten steel can be controlled by the amount of shielding gas injected, the immersion depth of the immersion nozzle, and the basicity of the flux used, and the combination of optimal conditions for each of these can be controlled. In combination, maximum Al 2 O 3 inclusions can be removed. However, conventional prior art, for example, JP-A-52-
As shown in No. 26318, etc., it is necessary to further regulate the viscosity of the molten flux according to the slab drawing speed. For this reason, the molten flux first becomes Al 2 O 3
We investigated how the viscosity changes when inclusions are absorbed. The results are shown in FIG.

【表】 この図は、第1表に示す基本組成を持つフラツ
クスについて、フラツクス中のAl2O3含有量がそ
れぞれ5、10、15、20、25%になるようにAl2O3
の水準を変えて添加し、その試料の1300℃におけ
る粘度を測定し、Al2O3が0%のときの粘度を基
準にしての各Al2O3レベルの粘度変化指数を示し
たものである。〇印はフラツクス、◇印はフラ
ツクス、△印はフラツクスである。いずれの
フラツクスも15%以上のAl2O3量になると急激に
粘度が上昇する。この変化を回帰分析した結果
(2′)式を得た。 y=0.55+0.34×1.12x ……(2′) ここでyは変化量、xはフラツクス中のAl2O3
含有量(重量%)である。この(2′)式で計算し
た値を第1図に●印で示した。実測値とよく一致
していることが判る。 この(2′)式を利用してフラツクスが溶融後
Al2O3介在物を吸収したときの粘度ηxは(2)式によ
つて求めることができる。 ηx=(0.55+0.34×1.12x)/(0.55+0.34×1.
12x0)η(2) ここでηはAl2O3吸収前のフラツクスの1300℃
における粘度(Poise)、x0はフラツクスがもとも
と含有しているAl2O3量(%)、xはフラツクス
が溶融後Al2O3介在物を吸収したときのAl2O3
(%)である。なおこの関係からも明らかなよう
にフラツクスがもともと含有しているAl2O3は出
来るだけ低目に制限しておくことが望ましい。 さらに鋳片引抜速度と良好な鋳片を得るための
粘度ηxとは明確な関係がある。即ち本発明者らの
知見によると良好な鋳片を得るための粘度は(3)式
で示される範囲にある。 この関係は粘度ηxの異なる鋳造条件で鋳造をお
こない適正粘度範囲を求めたものである。 この時の鋳造は、Si0.01〜0.03%、Mn0.1〜0.2
%、Al0.004〜0.007%、C0.04〜0.11%のアルミキ
ルド鋼を、鋳型サイズ厚さ210mm、幅950〜2100
mm、鋳片引抜速度0.8〜1.8m/minの範囲、フラ
ツクスは1300℃における粘度が0.4、0.6、1.1、
1.6、2.1、3.2、3.8Poiseでその時の塩基度Bがそ
れぞれ2.71、2.42、1.99、1.82、1.71、1.45、1.36
のものを使用し、シールド用Ar吹込み量は40〜
80/min・m2、浸漬ノズルの浸漬深さは160〜
180mmの範囲でおこなつた。 第2図は、鋳片の引抜速度を横軸に、(2)式で求
めた粘度ηxを縦軸にとり鋳片表面1m2当りに発生
した割れおよびスラグ捲込み等の欠陥の個数が7
個以下の場合を〇印、7個を超えるものを△印で
示したものである。同図より、鋳造速度が増加す
る場合低粘度パウダーを使用することが好ましい
が、過度に低下させると、かえつて鋳片表面欠陥
を増加させることになり、(3)式で示す範囲の粘度
条件で鋳造する必要があることがわかる。 1.0/V≦ηx≦4.0/V ……(3) ここでVは鋳片引抜速度(m/min)で、ηx
溶融フラツクスがAl2O3介在物を吸収した時の(2)
式によつて求めた粘度(Poise)である。 (3)式において、粘度が1.0/V未満であると鋳型と 鋳片の間に流入するフラツクスが過剰になり、局
所的な流入過剰も生じ溶融フラツクス流入不良に
基づく割れが生じる。又、流入過剰による溶融フ
ラツクスプール層の不足により、スラグ捲込みが
発生する。一方、粘度が4.0/Vを超えると、溶融フ ラツクスの流動性が劣化し、鋳型と鋳片の間へ溶
融フラツクスが均一に流入せず、割れが発生す
る。又この流入不良が発生すると溶融フラツクス
の更新が遅くなるため、溶融フラツクス中の
Al2O3量が多くなり更に流動性を劣化するし、又
溶融フラツクスのAl2O3介在物吸収力が低下し鋳
片のAl2O3介在物捲込みが増加する。 以下実施例により、本発明の効果を更に具体的
に示す。 実施例 供試鋼としてC0.06%、Si0.02%、Mn0.15%、
Al0.007%、のアルミキルド鋼を使用した。鋳型
サイズは厚さ210mmと245mm、幅850〜2100mmで鋳
片引抜速度は1.0〜1.8m/minの範囲でおこなつ
た。 シールドガスはArを使用し鋳型内単位断面積
(m2)当り0〜160/minの範囲で実施した。又
浸漬ノズルは、逆Y字型溶鋼吐出口のものを使用
し、浸漬深さは、ノズル吐出口の中心位置から溶
鋼表面までの距離が100〜250mmの範囲で実施し
た。なお溶鋼表面位置の変化は±5mm以内になる
よう制御しておこなつた。 又供試したフラツクスは原材料の配合混合、そ
して混合物を溶解粉砕し、これに溶融速度調整剤
と造粒剤を加え造粒し、製造した。 原材料は石灰石、硅砂、ソーダ灰、炭酸リチウ
ム、蛍石、弗化ソーダ、アルミナ、マグネシアを
使用し、溶融速度調整剤としてはコークスの微粉
とカーボンブラツクを使用した。そのフラツクス
の組成、塩基度、粘度は第2表に示す通りであ
り、A〜Gの7種のフラツクスを調整した。
[Table] This figure shows that for the fluxes having the basic composition shown in Table 1, Al 2 O 3 was added so that the Al 2 O 3 content in the flux was 5, 10, 15, 20, and 25%, respectively.
The viscosity of the sample at 1300℃ was measured by adding different levels of Al 2 O 3, and the viscosity change index for each Al 2 O 3 level is shown based on the viscosity when Al 2 O 3 is 0%. be. ○ mark is flux, ◇ mark is flux, △ mark is flux. The viscosity of any flux increases rapidly when the amount of Al 2 O 3 exceeds 15%. As a result of regression analysis of this change, equation (2') was obtained. y=0.55+0.34×1.12 x ...(2') Here, y is the amount of change, x is Al 2 O 3 in the flux
content (wt%). The values calculated using equation (2') are shown in Figure 1 with ●. It can be seen that the values match well with the measured values. Using this equation (2′), the flux is
The viscosity η x when Al 2 O 3 inclusions are absorbed can be determined by equation (2). η x = (0.55 + 0.34 x 1.12 x ) / (0.55 + 0.34 x 1.
12 x0 ) η(2) where η is the flux of 1300℃ before Al 2 O 3 absorption
viscosity ( Poise ) at _ _ It is. As is clear from this relationship, it is desirable to limit the Al 2 O 3 originally contained in the flux to as low a level as possible. Furthermore, there is a clear relationship between the slab drawing speed and the viscosity η x required to obtain a good slab. That is, according to the findings of the present inventors, the viscosity for obtaining a good slab is within the range shown by equation (3). This relationship was obtained by determining the appropriate viscosity range by performing casting under different casting conditions of viscosity η x . The casting at this time is Si0.01~0.03%, Mn0.1~0.2
%, Al0.004~0.007%, C0.04~0.11% aluminum killed steel, mold size thickness 210mm, width 950~2100
mm, the slab drawing speed ranges from 0.8 to 1.8 m/min, and the flux has a viscosity of 0.4, 0.6, 1.1 at 1300℃,
At 1.6, 2.1, 3.2, 3.8 Poise, the basicity B at that time is 2.71, 2.42, 1.99, 1.82, 1.71, 1.45, 1.36, respectively.
The amount of Ar injection for shielding is 40 ~
80/min・m 2 , immersion depth of immersion nozzle is 160~
This was done within a range of 180mm. Figure 2 shows the number of defects such as cracks and slag entrainment occurring per 1 m2 of slab surface, with the horizontal axis representing the drawing speed of the slab and the vertical axis representing the viscosity η x determined by equation (2).
If the number is less than 7, it is marked with ○, and if it is more than 7, it is marked with △. From the same figure, it is preferable to use a low-viscosity powder when the casting speed is increased, but if the casting speed is decreased excessively, the surface defects of the slab will increase. It turns out that it is necessary to cast it with 1.0/V≦η x ≦4.0/V …(3) Here, V is the slab drawing speed (m/min), and η x is the time when the molten flux absorbs Al 2 O 3 inclusions (2)
This is the viscosity (Poise) determined by the formula. In equation (3), if the viscosity is less than 1.0/V, excessive flux will flow between the mold and the slab, and local excess flow will occur, causing cracks due to insufficient flow of molten flux. In addition, slag entrainment occurs due to insufficient molten flux spool layer due to excessive inflow. On the other hand, when the viscosity exceeds 4.0/V, the fluidity of the molten flux deteriorates, and the molten flux does not flow uniformly between the mold and the slab, causing cracks. Also, if this inflow failure occurs, the renewal of the molten flux will be delayed, so the amount of flux in the molten flux will increase.
As the amount of Al 2 O 3 increases, the fluidity is further deteriorated, and the ability of the molten flux to absorb Al 2 O 3 inclusions decreases, and the entrainment of Al 2 O 3 inclusions in the slab increases. The effects of the present invention will be illustrated in more detail with reference to Examples below. Example: Sample steel: C0.06%, Si0.02%, Mn0.15%,
Used aluminum killed steel with Al0.007%. The mold sizes were 210 mm and 245 mm thick, 850 to 2100 mm wide, and the slab drawing speed was 1.0 to 1.8 m/min. Ar was used as the shielding gas, and the rate was 0 to 160/min per unit cross-sectional area (m 2 ) in the mold. The immersion nozzle had an inverted Y-shaped molten steel discharge port, and the immersion depth was such that the distance from the center of the nozzle discharge port to the surface of the molten steel was 100 to 250 mm. The change in the molten steel surface position was controlled to within ±5 mm. The tested flux was manufactured by mixing the raw materials, melting and pulverizing the mixture, and adding a melting rate regulator and a granulating agent to the mixture and granulating it. The raw materials used were limestone, silica sand, soda ash, lithium carbonate, fluorite, sodium fluoride, alumina, and magnesia, and the melting rate regulators were coke fine powder and carbon black. The composition, basicity, and viscosity of the fluxes are shown in Table 2, and seven types of fluxes A to G were prepared.

【表】【table】

【表】【table】

【表】【table】

【表】 これらの条件で連続鋳造をおこなつた結果が第
3表である。 実施例No.1〜No.7はシールドガス量をいろいろ
かえて検討したものである。 第3図にシールドAr量(/min・m2)と
Al2O3介在物が溶鋼から排出される量(g/
min・m2)との関係を示した。同図から判るよう
に、Ar吹込みなしを除いてAr吹込み量を増す程
排出されるAl2O3介在物量は増加する。実施例No.
1のAr吹込みなしでAl2O3介在物の排出量が多く
なる現象は、溶鋼が浸漬ノズル内を通過するとき
の酸化が大きく、鋳型内に入つてくるAl2O3介在
物の量が大きくなつたためと考えられる。その結
果Al2O3介在物の排出量が多いにもかかわらず、
鋳片の介在物捲込み、スリバー疵の発生が多かつ
た。実施例No.2のAr吹込み量18/min・m2
は、Al2O3介在物の排出量が25g/min・m2でス
リバー疵の発生がみられた。実施例No.3、No.4、
No.5のAr吹込み量が20、70、120/min・m2
はAl2O3介在物排出量が35、230、460g/min・
m2でスリバー疵の発生等が少ない良好な鋳片が得
られた。実施例No.6、No.7のAr吹込み量140、
160/min・m2ではAl2O3介在物の排出量は520、
600g/min・m2と多かつたがスラグ捲込みスリ
バー疵の発生がみられた。これはAr吹込み量が
過大のためハブリング現象が大きくなり過ぎ溶鋼
表面の波立ちが大きくなり、このためスラグ捲込
みを生じ、又このスラグ捲込みによるスリバー疵
が発生したものと考えられる。 実施例No.4およびNo.8〜No.11は浸漬ノズルの浸
漬深さをいろいろ変えた場合について調べたもの
である。第4図にノズル浸漬深さとAl2O3介在物
の排出量の関係を示す。同図から判るように浸漬
深さが深くなる程Al2O3介在物排出量は小さくな
る。実施例No.8の浸漬深さ110mmでは、Al2O3
在物の排出量は550g/min・m2と大きいが溶鋼
の湯面変動のためと考えられるスラグ捲込みスリ
バー疵が発生した。実施例No.9、No.4、No.10の浸
漬深さ130、170、210mmではAl2O3排出量が280、
230、160g/min・m2で鋳片品質も良好であつ
た。実施例No.11の浸漬深さ230mmでは溶鋼表面層
の温度が低くなり過ぎる傾向がみられAl2O3介在
物排出量も20g/min・m2と小さく鋳片の表面割
れ、スラグ捲込み、スリバー疵の発生がみられ
た。 実施例No.4およびNo.12〜No.17においては鋳型内
に添加するフラツクスの塩基度の影響について比
較した。第5図にフラツクス塩基度とAl2O3介在
物の排出量の関係を示した。同図から明らかなよ
うにフラツクスの塩基度が高くなる程、Al2O3
在物の排出量は大きくなる。実施例No.12のフラツ
クスの塩基度1.27は、Al2O3介在物排出量20g/
min・m2でスリバー疵の発生がみられた。実施例
No.13のフラツクス塩基度1.37は、Al2O3介在物排
出量は40g/min・m2であるが、フラツクス粘度
不適正と考えられる鋳片表面割れの発生がみられ
た。実施例No.4およびNo.14、No.15、No.16のフラツ
クス塩基度がそれぞれ1.78、1.42、2.01、2.49に
ついては、Al2O3介在物の排出量は230、50、
330、450g/min・m2で鋳片品質も良好であつ
た。実施例No.17はフラツクス塩基度2.69でAl2O3
介在物の排出量は510g/min・m2と多いがスラ
グ捲込みが認められた。これは第2表に示したフ
ラツクスGがA〜Fのフラツクスに比較し、粘度
が低くこのためフラツクスの流出速度が過大にな
つたためと考えられる。 次に実施例No.3、No.4、No.5およびNo.13〜No.26
で鋳片引抜速度とフラツクスの粘度の関係を対比
した。第6図にその結果をまとめて示した。 同図は横軸は鋳片引抜速度で縦軸の粘度はフラ
ツクスのAl2O3吸収量を測定し(2)式によつて求め
たηxである。●印は鋳片表面の割れスラグ捲込
み、スリバー疵の発生がみられたもの、〇印は欠
陥のない良好な鋳片が得られたものを示す。同図
から明らかなように良好な鋳片を得るための粘度
は(3)式で示す範囲である。ηxが4.0/Vを超える実施 例No.13、No.18、No.22、No.23およびηxが1.0/V未満
の 実施例No.17、No.21、No.26ではいずれも鋳片表面割
れ、あるいはスラグ捲込み、スリバー疵の発生が
認められた。 以上実施例に基づいて本発明の効果を述べた
が、本発明は従来明らかでなかつた鋼の連続鋳造
におけるシールドガス吹込み量、浸漬ノズルの浸
漬深さ、フラツクスの塩基度、粘度などについて
の個々の条件の定量的把握、又その組合わせによ
る効果等を究明し、アルミキルド鋼のAl2O3介在
物の排出におよぼすこれら条件の影響を定量的に
把握し、これら条件の組合わせにより、従来の知
見にないアルミキルド鋼のまつたく新しい連続鋳
造法を提供することを可能としたものであり、産
業の発展に貢献する所極めて顕著なものがある。
[Table] Table 3 shows the results of continuous casting under these conditions. In Examples No. 1 to No. 7, the amount of shielding gas was varied. Figure 3 shows shielding Ar amount (/min・m 2 ) and
Amount of Al 2 O 3 inclusions discharged from molten steel (g/
min・m 2 ). As can be seen from the figure, the amount of Al 2 O 3 inclusions discharged increases as the amount of Ar injection increases, except in the case without Ar injection. Example No.
The phenomenon in which the amount of Al 2 O 3 inclusions is increased without Ar injection in step 1 is because the oxidation of molten steel is large when it passes through the immersion nozzle, and the amount of Al 2 O 3 inclusions entering the mold is large. This is thought to be because it has grown larger. As a result, despite the large amount of Al 2 O 3 inclusions discharged,
There were many occurrences of inclusions in the slab and sliver defects. In Example No. 2, when the Ar injection rate was 18/min·m 2 , the occurrence of sliver defects was observed when the discharge rate of Al 2 O 3 inclusions was 25 g/min·m 2 . Example No. 3, No. 4,
When the Ar injection rate of No. 5 is 20, 70, and 120/min・m2 , the Al 2 O 3 inclusion discharge amount is 35, 230, and 460 g/min・
A good slab with less occurrence of sliver defects was obtained at m2 . Example No. 6, No. 7 Ar injection amount 140,
At 160/min・m2 , the emission amount of Al 2 O 3 inclusions is 520,
Although the amount was 600 g/min・m 2 , slag rolling-in sliver defects were observed. This is thought to be because the amount of Ar injection was too large, which caused the hub ring phenomenon to become too large, resulting in large ripples on the surface of the molten steel, which caused slag entrainment, and this slag entrainment caused sliver defects. In Examples No. 4 and No. 8 to No. 11, cases were investigated in which the immersion depth of the immersion nozzle was varied. FIG. 4 shows the relationship between the nozzle immersion depth and the amount of Al 2 O 3 inclusions discharged. As can be seen from the figure, the deeper the immersion depth, the smaller the amount of Al 2 O 3 inclusions discharged. At an immersion depth of 110 mm in Example No. 8, the amount of Al 2 O 3 inclusions discharged was as large as 550 g/min·m 2 , but slag entrainment sliver defects occurred, which was thought to be due to fluctuations in the molten steel level. At the immersion depths of 130, 170, and 210 mm in Examples No. 9, No. 4, and No. 10, the Al 2 O 3 emissions were 280 mm,
The slab quality was also good at 230 and 160g/min・m2 . At the immersion depth of 230 mm in Example No. 11, the temperature of the molten steel surface layer tends to become too low, and the amount of Al 2 O 3 inclusions discharged is also small at 20 g/min・m 2 , causing surface cracks in the slab and slag entrainment. , sliver defects were observed. In Examples No. 4 and No. 12 to No. 17, the influence of the basicity of the flux added into the mold was compared. Figure 5 shows the relationship between flux basicity and the amount of Al 2 O 3 inclusions discharged. As is clear from the figure, the higher the basicity of the flux, the greater the amount of Al 2 O 3 inclusions discharged. The basicity of the flux of Example No. 12 is 1.27, and the amount of Al 2 O 3 inclusions discharged is 20 g/
Sliver defects were observed at min·m 2 . Example
For No. 13, which had a flux basicity of 1.37, the amount of Al 2 O 3 inclusions discharged was 40 g/min·m 2 , but cracks on the surface of the slab were observed, which was considered to be due to inappropriate flux viscosity. For Example No. 4 and No. 14, No. 15, and No. 16 whose flux basicity is 1.78, 1.42, 2.01, and 2.49, respectively, the discharge amount of Al 2 O 3 inclusions is 230, 50,
The slab quality was also good at 330 and 450g/min・m2 . Example No. 17 has a flux basicity of 2.69 and is Al 2 O 3
The amount of inclusions discharged was high at 510g/min・m2 , but slag entrainment was observed. This is considered to be because flux G shown in Table 2 had a lower viscosity than fluxes A to F, and as a result, the flow rate of the flux became excessive. Next, Examples No. 3, No. 4, No. 5 and No. 13 to No. 26
The relationship between slab drawing speed and flux viscosity was compared. Figure 6 summarizes the results. In the figure, the horizontal axis is the slab withdrawal speed, and the vertical axis is the viscosity, which is η x determined by measuring the amount of Al 2 O 3 absorbed by the flux and using equation (2). ● marks indicate slabs with cracks on the surface of the slabs, slag entrainment, and sliver defects; ○ marks indicate slabs with no defects and good quality. As is clear from the figure, the viscosity required to obtain a good slab is within the range shown by equation (3). In Examples No. 13, No. 18, No. 22, and No. 23 where η x exceeds 4.0/V, and in Examples No. 17, No. 21, and No. 26 where η x is less than 1.0/V, Cracks on the slab surface, slag entrainment, and sliver defects were observed. The effects of the present invention have been described above based on the examples. However, the present invention provides improvements in the amount of shielding gas blown into continuous casting of steel, the immersion depth of the immersion nozzle, the basicity of the flux, the viscosity, etc., which were not previously clear. By quantitatively understanding individual conditions and investigating the effects of their combinations, quantitatively understanding the effects of these conditions on the emission of Al 2 O 3 inclusions from aluminum killed steel, and by combining these conditions, It has made it possible to provide a completely new continuous casting method for aluminium-killed steel that has not been found in the past, and its contribution to the development of industry is extremely significant.

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

第1図はフラツクス中のAl2O3量の増加による
粘度の相対変化を示す図、第2図は鋳片引抜速度
と粘度ηxとの関係において良好な鋳片が得られる
領域を示す図、第3図は実施例についてシールド
用Arガス吹込み量とAl2O3介在物排出量との関係
を示す図、第4図は実施例について浸漬ノズルの
浸漬深さとAl2O3介在物の排出量との関係を示す
図、第5図は実施例についてフラツクスの塩基度
BとAl2O3介在物の排出量との関係を示す図、第
6図は実施例について鋳片引抜速度と粘度ηxとの
関係を示す図である。
Figure 1 is a diagram showing the relative change in viscosity due to an increase in the amount of Al 2 O 3 in the flux, and Figure 2 is a diagram showing the region where good slabs can be obtained in the relationship between slab drawing speed and viscosity η x . , Fig. 3 is a diagram showing the relationship between the amount of shielding Ar gas blown in and the amount of Al 2 O 3 inclusions discharged for the example, and Fig. 4 is a diagram showing the relationship between the immersion depth of the immersion nozzle and the Al 2 O 3 inclusions for the example. Figure 5 is a diagram showing the relationship between the basicity B of flux and the discharge amount of Al 2 O 3 inclusions for Examples, and Figure 6 is a diagram showing the relationship between the flux basicity B and the discharge amount of Al 2 O 3 inclusions for Examples. FIG. 2 is a diagram showing the relationship between viscosity η x and

Claims (1)

【特許請求の範囲】 1 アルミキルド鋼の連続鋳造において、不活性
ガスを鋳型単位断面積(m2)あたり20/min〜
130/minの範囲で溶鋼に吹込み、且つ浸漬ノ
ズルの溶鋼吐出口の中心が溶鋼表面から120mm〜
220mmの範囲で浸漬し、鋳型内添加フラツクスを
(1)式によつて求めた塩基度Bを1.3以上に規制し
てAl2O3介在物を鋳型単位断面積(m2)あたり30
g/min以上溶鋼中より排出し、且つその排出さ
れたAl2O3介在物を吸収した鋳型内溶融フラツク
スの粘度ηx(Poise)を(2)式によつて求め、それが
鋳片引抜速度に応じて(3)式で求められる範囲にな
るよう規制して鋳造することを特徴とするアルミ
キルド鋼の連続鋳造法。 B= 1.53・CaO+1.51・MgO+1.37・K2O+1.94・Na2O+1.53
・CaF2+3.55・Li2O+3.27・NaF/1.48・SiO2+0.36・T
iO2+0.10・Al2O3 ……(1) 但し、各成分は重量% ηx=(0.55+0.34×1.12x)/(0.55+0.34×1.12
x0)η(2) 但し、η:Al2O3吸収前のフラツクスの1300℃
における粘度(Poise) x0:フラツクスが元々含有しているAl2O3(%) x:Al2O3介在物を吸収した溶融フラツクス中の
Al2O3(%) 1.0/V≦ηx≦4.0/V (3) 但し、V:鋳片引抜速度(m/min)
[Claims] 1. In continuous casting of aluminum-killed steel, inert gas is applied at 20/min or more per mold unit cross-sectional area (m 2 ).
Blow into the molten steel at a rate of 130/min, and ensure that the center of the molten steel outlet of the immersion nozzle is 120 mm or more from the molten steel surface.
Immerse within a range of 220mm to add flux inside the mold.
The basicity B determined by formula (1) is controlled to 1.3 or more, and the Al 2 O 3 inclusions are reduced to 30% per unit cross-sectional area (m 2 ) of the mold.
The viscosity η A continuous casting method for aluminum killed steel, which is characterized by controlling the casting speed to fall within the range determined by equation (3). B= 1.53・CaO+1.51・MgO+1.37・K2O +1.94・Na2O +1.53
・CaF 2 +3.55・Li 2 O+3.27・NaF/1.48・SiO 2 +0.36・T
iO 2 +0.10・Al 2 O 3 ...(1) However, each component is weight% η x = (0.55 + 0.34 x 1.12 x ) / (0.55 + 0.34 x 1.12
x0 )η(2) However, η: 1300℃ of flux before Al 2 O 3 absorption
Viscosity (Poise) x 0 : Al 2 O 3 originally contained in the flux (%)
Al 2 O 3 (%) 1.0/V≦η x ≦4.0/V (3) However, V: Slab drawing speed (m/min)
JP21548882A 1982-12-10 1982-12-10 Continuous casting method of aluminum killed steel Granted JPS59107754A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21548882A JPS59107754A (en) 1982-12-10 1982-12-10 Continuous casting method of aluminum killed steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21548882A JPS59107754A (en) 1982-12-10 1982-12-10 Continuous casting method of aluminum killed steel

Publications (2)

Publication Number Publication Date
JPS59107754A JPS59107754A (en) 1984-06-22
JPS6315060B2 true JPS6315060B2 (en) 1988-04-02

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ID=16673209

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21548882A Granted JPS59107754A (en) 1982-12-10 1982-12-10 Continuous casting method of aluminum killed steel

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Country Link
JP (1) JPS59107754A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6289557A (en) * 1985-10-11 1987-04-24 Sumitomo Metal Ind Ltd Continuous casting method
JPH01180753A (en) * 1987-12-28 1989-07-18 Kawasaki Steel Corp Continuous casting method
JP2672577B2 (en) * 1988-06-18 1997-11-05 新日本製鐵株式会社 Continuous casting method for low carbon steel
JP4345457B2 (en) * 2003-11-27 2009-10-14 Jfeスチール株式会社 High Al steel high speed casting method
JP4751283B2 (en) * 2006-02-01 2011-08-17 新日本製鐵株式会社 Continuous casting powder and steel continuous casting method

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5211312B2 (en) * 1972-07-14 1977-03-30
AT331437B (en) * 1973-06-14 1976-08-25 Voest Ag CONTINUOUS STEEL CASTING PROCESS AND DEVICE FOR ITS IMPLEMENTATION
AT331438B (en) * 1973-06-14 1976-08-25 Voest Ag CONTINUOUS STEEL CONTINUOUS STEEL CASTING PROCESS AND SYSTEM FOR IMPLEMENTING THE PROCESS
JPS5417329A (en) * 1977-07-09 1979-02-08 Sumitomo Metal Ind Continuous casting method
JPS55154520A (en) * 1979-02-23 1980-12-02 Mobay Chemical Corp Particulate slagging composition for extended optimum continuous casting of steel
JPS5641055A (en) * 1979-09-12 1981-04-17 Nippon Steel Corp Continuous casting method
JPS5942589B2 (en) * 1981-04-28 1984-10-16 新日本製鐵株式会社 Continuous steel casting method

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