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JPH0573504B2 - - Google Patents
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JPH0573504B2 - - Google Patents

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Publication number
JPH0573504B2
JPH0573504B2 JP23694789A JP23694789A JPH0573504B2 JP H0573504 B2 JPH0573504 B2 JP H0573504B2 JP 23694789 A JP23694789 A JP 23694789A JP 23694789 A JP23694789 A JP 23694789A JP H0573504 B2 JPH0573504 B2 JP H0573504B2
Authority
JP
Japan
Prior art keywords
wire
iron
mold
alloy
coated
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 - Lifetime
Application number
JP23694789A
Other languages
Japanese (ja)
Other versions
JPH0399751A (en
Inventor
Takeshi Sugawara
Yasushi Ishibashi
Ichiro Kudo
Shuichi Myabe
Mitsuru Nikaido
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 JP23694789A priority Critical patent/JPH0399751A/en
Publication of JPH0399751A publication Critical patent/JPH0399751A/en
Publication of JPH0573504B2 publication Critical patent/JPH0573504B2/ja
Granted legal-status Critical Current

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Description

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

産業上の利用分野 本発明は、鋳型内への鉄被覆合金ワイヤーを添
加し、鋳片表層部がタンデイツシユ内溶鋼と同一
成分からなり、鋳片コア部のみに合金成分を含有
せしめた鋳込み複合鋼材を製造する方法に関す
る。 従来の技術 鋼材の表層部とコア部とで異なる鋼種の特性を
有る複合鋼材は、付加価値の高い鋼材として使用
され、最近連続鋳造による製造について報告がな
されている。例えば、「鉄と鋼」72(1986)、S985
における「クラツド鋼丸ビレツトの連続鋳造法」、
或いは「材料とプロセス」1(1988)、S298での
「ステンレス鋼中空丸プルームの連続鋳造法」が
あり、これら鋳ぐるみ法による複合鋼材の製造方
法に関する。 複合鋼材そのの製造方法としては、鋳型内へ合
金元素を添加するコア添加法が知られている。例
えば、特公昭55−14847号には、コア部に鉄被覆
チタン充填ワイヤーを添加するホーロー溶鋼板の
製造方法が、特開昭62−142053号には、鉄被覆硫
黄充填ワイヤーによりコア部に硫黄を添加する硫
黄快削鋼の製造方法が開示されている。 発明が解決しようとする課題 コア添加法による鋳込複合鋼材の製造は、タン
デイツシユ内溶鋼成分と同一成分からなる所定厚
みの表層部を確保し、更にそのコア部を合金添加
により成分を所定範囲内に調整することにより、
表層部とコア部が異なる成分からなる複合鋼材を
得ようとするものである。 以上の方法の課題は、第1図のように表層部を
形成する溶鋼成分のプールとコア部を形成する添
加合金を含む溶鋼成分のプールを連鋳片内で分離
して保持することが必要であり、このため合金を
その内部に充填した鉄被覆合金ワイヤーの溶解位
置制御が重要な技術となる。 鋳型内の溶鋼流動は、一般に浸漬ノズルの吐出
孔からの吐出流の影響による鋳型上部(図中A
部)の上昇循環流領域とその下部(図中B部)の
上昇循環流が鎮静化した領域に大別される。 ここで上述した溶鋼成分の異なる2つのプール
を確保するには、B部でかつ所要の表層部厚みが
確保出来る位置に鉄被覆合金ワイヤーを投入し溶
解を完了させることが複合材を製造する上で必要
である。 しかしながら上記の観点から鋳型より過度に下
部(図中C部)で溶解させようとして溶解しにく
いワイヤーを用いた場合には、ワイヤーの外周に
鋳型内の溶鋼が凝固付着したまま鋳片内に残存し
たり、またたとえワイヤーが溶解しても均一な合
金の混合、拡散が行われず合金が局部的に濃化す
る問題がある。 本発明では、連続鋳造による複合鋼材の製造に
おいて、鉄被覆ワイヤーの溶解位置制御方法につ
いて最適化をはかると共に、コア添加法により安
定して複合材を製造できるようにしたものであ
る。 課題を解決するための手段 本発明は以上の課題を解決するものであり、以
下にまず鉄被覆ワイヤーの溶解位置コントロール
手段について述べる。製造しようとする複合材の
目標とする表層部厚みをLs(m)とするとき、鋳片内
湯面からのワイヤー溶解位置L(m)は凝固式から(1)
式で求めることが出来る。 L=(LS/K)2・VC ……(1) ここでKは凝固係数(m/min1/2)、VCは鋳造
速度(m/min)である。 一方、ワイヤー供給速度をVW(m/min)とす
れば、鋳片内に供給したワイヤーが溶解位置Lま
で到達する時間T(min)(以下溶解時間という)
は、(2)式で示される。 T=L/VW ……(2) (1)および(2)式から、(3)式が得られる。 L=(LS/K)2・VC=VW・T ……(3) このように、目標とする表層部厚みLS、鋳造速
度VCが与えられれば、ワイヤーの溶解すべき位
置Lが定まり、これはワイヤー投入速度VWとワ
イヤー溶解時間Tの積により表すことが出来る。 発明者らは、ワイヤー溶解時間を添加しようと
する合金を被覆する鉄ワイヤー部の肉厚t、径D
により制御しようとした。ここで当然ながらワイ
ヤーは溶鋼中を通過中、溶鋼の凝固付着、溶解の
過程を経るが、ここで言う溶解時間は最終的に鉄
被覆部が溶解し、中に充填された合金元素を吐き
出す時点を言う。またここで、溶解時間として鉄
被覆部に着眼しているのは、一般に鉄被覆ワイヤ
ー内に充填する合金は粉体状にて充填されるため
粉体間の空気層の存在により伝熱抵抗が大きく、
鉄被覆部に比べ溶鋼からの伝熱が遅いという理由
による。 第2図に示す如く、発明者の調査でも、溶鋼温
度を融点直上に保ち、かつ溶鋼とワイヤーの鉄被
覆の成分がほぼ同等のもので溶解時間を測定した
結果によつても、鉄被覆部の肉厚t、径Dにより
溶解時間が決まり、おおよそ第3図のように鉄被
覆断面積により表せる。 以上から、鉄被覆ワイヤーの溶解時間を決定す
る因子を明らかにし、更に実用上にこれらの因子
と溶解位置Lの関係を明確にするため、実際の複
合材製造を行い、(4)式にように、鉄被覆ワイヤー
の溶解制御を行う指標となる式を得た。 L=C3・ρs・S・VW ……(4) ここで、Lは溶解位置(m)、ρsはワイヤー被覆部
の密度(Kg/m3)、VWはワイヤーの投入速度
(m/min)、Sは鉄被覆ワイヤーの断面積(m2)、
C3は係数で0.3〜0.6程度である。 Sは、鉄被覆ワイヤーの内径Di(m)と外径DO(m)
を使つて次式で求まる。 S=π/4・(DO 2−Di 2) ……(5) (4)式は、溶解位置Lを供給するワイヤーの熱容
量によりコントロールする考えに基づいた式であ
り、係数は、鋳型内の溶鋼温度、鋳型サイズによ
り多少変動するので、上記範囲の中で最も適当な
係数を選定してワイヤーの投入速度制御を行えば
良い。 ここで、鉄被覆ワイヤーの断面形状は、上述の
如く円形でも、或いは楕円形、角型その他の形状
でも、鉄被覆ワイヤーの断面積Sをそれぞれの形
状に応じて同様に取り扱うことにより(4)式を適用
してよい。 以上により鉄被覆ワイヤーにより溶解位置Lを
調整する方法についての概略を述べた。 次に、コア部への合金元素添加の調整供給方法
について述べる。 ワイヤー溶解位置での鋳片の凝固シエル内溶鋼
断面積をA(m2)、溶鋼の密度をρM(Kg/m3)、コア
部への合金添加目標濃度差(上昇分)をΔC(%)、
ワイヤー内径をDi(m)、ワイヤー内合金元素の充填
密度をρc(Kg/m3)、合金元素の添加歩留をη
(%)、溶解に供するワイヤー本数N本とすれば、
(6)式の物質収支式が求まる。 A×VC×ρM×ΔC =π/4・Di 2×ρc×VW×η×N ……(6) ここでワイヤーにより供給される合金添加量Q
は Q=π/4・Di 2×ρc×VW×N ……(7) であるから、鉄被覆ワイヤーの操作因子は以下の
ように表せる。 Di 2VW=Q(ρc・π/4・N) ……(8) 以上から所望の溶解位置L(表層厚LS)を満足
しつつコア部に所望の合金量Qを添加する鉄被覆
ワイヤー条件は、(4)式および(8)式を満足する鉄被
覆ワイヤーの肉厚、径、投入速度等を組み合わせ
ることにより得られる。 以上の方法により、コア添加法による複合材製
造上のワイヤーの溶解位置制御方法の考え方を示
した。 以上述べた方法により複合材を製造するにあた
つてのワイヤーの必要溶解位置およびワイヤー仕
様の概略を決定出来るが、ワイヤーの溶解位置が
前述の課題である鋳型内の溶鋼の流動状態を勘案
して十分であるかの判断条件を規定するのが、次
なる判明の骨子であり、以下にその詳細を述べ
る。 第1図に示した鋳型内A部でワイヤーの溶解が
行われる場合、添加合金の混合、拡散が複合材製
造上の問題となる。この点について水モデル試験
による鋳型内の上昇循環流の調査結果を第4図に
示すが、鋳型サイズが大きいほど鋳型内の混合領
域は湯面から深い所まで存在し、概略ノズル浸漬
深さを基準として鋳型の長辺幅の(1〜2)倍程
度である。 したがつて、鋳型内A部への添加合金の混合、
拡散を防止するためには、ワイヤーの溶解位置L
(m)は、次式とすることが必要である。 L>(C1×H+LN)÷1000 ……(9) ここで、Hは鋳型サイズの長辺幅(m)、LNはノ
ズルの浸漬深さ(mm)、C1は係数で1〜1.5程度で
ある。 さらに、本発明者らは、浸漬ノズルの吐出孔を
変更することにより鋳型内流動の最適化を図る手
段、すなわち(9)式で規定される溶解位置最浅制約
の緩和手段を開示する。 (1) 旋回ノズル方式 浸漬ノズルの吐出孔を鋳型内壁面に対して、
第5図aのように傾斜して噴射することによ
り、吐出流の運動エネルギーが鋳型下法に及び
のを抑制することにより、第2図のA部を縮小
する方法である。特にこの方法は、鋳型サイズ
が大きい場合に有効に方法である。 (2) 浸漬ノズルのストレート化 従来の鋳型内壁面に向かう吐出孔に加え、第
5図bのように浸漬ノズルの底部に鋳型下方へ
吐出孔を新たに設けることにより前者の吐出孔
にて所要表層部厚み形成のための湯量を極力小
さい運動エネルギーで供給し、更に後者の吐出
孔にてコア形成用の湯量、並びに添加合金の均
一分散のための撹拌エネルギーを確保すること
に特徴がある。特にこの方法は、鋳型サイズが
小さい場合に有効な方法である。 以上複合材製造上の鉄被覆ワイヤーの溶解位置
についての場面からの必要最浅深さについての規
定とその制約条件の緩和方法について述べた。 次に、鉄被覆ワイヤーの溶解位置についての場
面からの限界最深深さについて述べる。限界最深
深さは鉄被覆ワイヤーの付着地金残存という問題
から規定するもので、第1図のB領域の下端の溶
鋼が加熱度ΔT(=溶鋼温度−融点)及び流動性
を消失した位置で定義するものである。この条件
は、鋳型の熱容量に対する凝固シエル成長による
抜熱による鋳型内溶鋼温度の低下により概略決ま
るものである。 (10)式の左辺の第2項は、鋳型内の凝固割合を定
義する式であり、左辺は鋳型内の未凝固割合
(%)を表現する。実湯テストなどから、鉄被覆
ワイヤーの付着地金残存が発生しない条件を求め
ると、ワイヤーの溶鋼位置Lにおける鋳片の未凝
固率が、40〜50%以上の領域で溶解を完了させる
必要がある。 1−K・(L/VC1/2・2(H+B)/(H×B)
>0.4〜0.5 ……(10) ここで、 Kは凝固係数(mm/min1/2)、Lは鉄被覆ワイヤ
ーの溶解位置(m)、VCは鋳造速度(m/min)、H
は鋳型の長辺幅(mm)、Bは鋳型の短辺厚み(mm)
を表す。 (10)式から溶解位置についての湯面からの限界最
深深さLは次式となる。 L<WC・((0.5〜0.6)×(H×B)/K・2(H+B
))2……(11) 以上をまとめると、鉄被覆ワイヤーの溶解位置
についての湯面からの最浅深さを(9)式にて規定
し、限界最深深さLを(11)式にて規定することによ
り、鉄被覆ワイヤーの溶解位置はC1を1〜1.5、
C2を0.5〜0.6とし、(12)式にて規定される。 C1×H×LN/1000<L<VC・(C2×(H×B)/K×2
(H+B))2 ……(12) 作 用 本発明は、その内部に添加合金元素を充填した
鉄被覆ワイヤーの溶解位置制御について述べたも
ので、第1の作用は、複合材製造上必要なワイヤ
ーの溶解位置の制御範囲を明らかにしたことであ
り、第2の作用は、鉄被覆ワイヤーの寸法および
投入速度を制御因子として、上記制御範囲に溶解
位置をコントロールしつつ、コア部に必要に応じ
た合金元素を供給する方法を明らかにしたことに
ある。 本発明による鉄被覆ワイヤーの溶解位置コント
ロールにより、良好な複合材の製造が可能とな
る。 実施例 以下に、コア部硫黄濃度の高い硫黄快削鋼の連
続鋳造に関する実施例について説明する。 転炉で0.06%C、0.02%Si、0.50%Mn、0.025
%P、0.02%S、0.015%Alの成分系の溶鋼を溶
製し、曲率半径12mの湾曲型連続機で、横断面サ
イズが162mm×162mmのビレツトを、5孔の浸漬ノ
ズル(水平4孔+垂直1孔の吐出孔を有す)を用
い、鋳造速度VC=1.8〜2.0m/minで鋳造した。 鋳型上部へワイヤー供給ガイドを設置し、ワイ
ヤー供給機を用いて鋳型と浸漬ノズルとの間から
鋳型内へ、粉末硫黄を充填した鉄被覆ワイヤーを
連続的に供給しながら鋳造した。 コア部硫黄濃度が0.150〜0.250%SのA鋼粒と
0.050〜0.100%SのB鋼主を製造するために硫黄
充填ワイヤーを2種類準備し、A鋼種用は外径
6.5mmφ、鉄被覆厚み0.9mm、B鋼種用は外径4.5mm
φ、鉄被覆厚み1.0mmとした。 尚、硫黄を添加しない鋳片表層部厚みの目標値
はいずれの鋼種においても10〜25mmとした。 第1表に、上記硫黄快削鋼の製造条件および得
られたビレツト鋳片から採取した横断面サンプル
における表層部厚みの測定結果、コア部硫黄濃度
の分析結果並びにコア部での地金残存の有無、硫
黄の局部濃化の有無についての観察結果を示し
た。 第6図は、鉄被覆ワイヤーの突入速度に対し
て、凝固後に表層部厚みから算出したワイヤーの
溶解位置を示している。 ここでは、上記実施例と対応付けて、本発明の
具体的適用方法について詳細に述べることとす
る。ここで基本条件として、鋳片サイズに対し、
VC=1.8m/minで凝固係数K=24mm/min1/2で表
層部厚みを15〜20mm確保するためには、(1)式から
ワイヤーの溶解位置を鋳片内湯面から0.7〜1.25
m深さにする必要がある。 これに対し、良好な複合材を製造するための鋳
片内での2つの溶鋼プールの分離条件およびワイ
ヤーの完全溶解条件を規定する(12)式は左辺がノズ
ル浸漬深さを0.2mとすると(0.36〜0.44)mと求
まり、また右辺は(1.28〜1.80)mの範囲にあ
り、上記の0.7〜1.25m深さにワイヤーの溶解位
置を制御すれば求める複合材が得られる見通しが
立つ。 次に、上記溶解位置に制御しつつ、コア部に目
標濃度を供給出来るワイヤー寸法およびワイヤー
供給速度を求める。今、コア部を0.050%Sから
0.200%Sに上昇させようとする必要硫黄量は
0.42Kg/minであり、硫黄の密度を2000Kg/m3
した物質収支の(8)式と、鉄被覆ワイヤーの溶解位
置制御の関係の(4)(5)式を連立させることで、ワイ
ヤーの外径DO=6.5mmφ、鉄被覆厚み0.9mm、ワイ
ヤーの供給速度VW=10.7m/min、鉄被覆部の供
給速度2.6Kg/minが求まる。この供給速度によ
り第6図の安定して複合材を製造可能な溶解位置
に制御出来る。 同様な方法が、鋳造条件が異なる場合にも適用
出来る。
Industrial Application Field The present invention is a cast composite steel material in which an iron-coated alloy wire is added to the mold, the surface layer of the slab is made of the same composition as the molten steel in the tundish, and the alloy component is contained only in the core of the slab. Relating to a method of manufacturing. BACKGROUND TECHNOLOGY Composite steel materials, in which the surface layer and core portion of the steel material have different characteristics, are used as high value-added steel materials, and there have recently been reports on their production by continuous casting. For example, "Tetsu to Hagane" 72 (1986), S985
``Continuous casting method for clad steel round billets'',
Alternatively, there is "Continuous casting method for stainless steel hollow round plumes" in "Materials and Processes" 1 (1988), S298, which relates to methods for producing composite steel materials by these casting methods. As a method for manufacturing composite steel materials, a core addition method in which alloying elements are added into a mold is known. For example, Japanese Patent Publication No. 55-14847 describes a method for manufacturing enameled molten steel sheets by adding iron-coated titanium-filled wire to the core, and Japanese Patent Publication No. 62-142053 describes a method for producing molten steel sheets by adding iron-coated sulfur-filled wire to the core. A method for manufacturing sulfur free-cutting steel is disclosed. Problems to be Solved by the Invention In the production of cast composite steel materials by the core addition method, a surface layer of a predetermined thickness is ensured with the same composition as the molten steel in the tundish, and the core part is further alloyed to keep the composition within a predetermined range. By adjusting to
The objective is to obtain a composite steel material in which the surface layer portion and the core portion have different components. The problem with the above method is that, as shown in Figure 1, it is necessary to separate and maintain the pool of molten steel components forming the surface layer and the pool of molten steel components containing additive alloys forming the core within the continuous slab. Therefore, controlling the melting position of iron-coated alloy wire filled with alloy becomes an important technology. The flow of molten steel in the mold is generally caused by the discharge flow from the discharge hole of the immersion nozzle.
The area is roughly divided into the upward circulation flow area (section B) and the area below it (section B in the figure) where the upward circulation flow has subsided. In order to secure the two pools with different molten steel compositions mentioned above, it is important to complete the melting by inserting the iron-coated alloy wire into the B part at a position where the required surface layer thickness can be secured. It is necessary. However, from the above point of view, if a wire that is difficult to melt is used in an attempt to melt excessively below the mold (section C in the figure), the molten steel in the mold solidifies and adheres to the outer periphery of the wire and remains in the slab. Furthermore, even if the wire is melted, there is a problem that uniform mixing and diffusion of the alloy is not achieved and the alloy locally becomes concentrated. In the present invention, in the production of composite steel materials by continuous casting, the method for controlling the melting position of the iron-coated wire is optimized, and the composite material can be stably manufactured using the core addition method. Means for Solving the Problems The present invention solves the above-mentioned problems, and first, means for controlling the melting position of the iron-coated wire will be described below. When the target thickness of the surface layer of the composite material to be manufactured is L s (m), the wire melting position L (m) from the melt surface in the slab can be calculated from the solidification equation (1).
It can be found using the formula. L=(L S /K) 2 ·V C (1) Here, K is the solidification coefficient (m/min 1/2 ) and V C is the casting speed (m/min). On the other hand, if the wire feeding speed is V W (m/min), it takes T (min) for the wire fed into the slab to reach the melting position L (hereinafter referred to as melting time).
is expressed by equation (2). T=L/V W ...(2) From equations (1) and (2), equation (3) is obtained. L = (L S /K) 2・V C = V W・T ...(3) In this way, if the target surface layer thickness L S and casting speed V C are given, the position where the wire should be melted is L is determined and can be expressed as the product of the wire feeding speed V W and the wire melting time T. The inventors determined that the thickness t and diameter D of the iron wire portion covering the alloy to which the wire melting time is to be added are
tried to control it. Naturally, while passing through the molten steel, the wire goes through the process of solidification, adhesion, and melting of the molten steel, but the melting time referred to here is the time when the iron coating finally melts and the alloying elements filled inside are discharged. say. In addition, here, we are focusing on the iron-coated part as the melting time because the alloy that is filled into the iron-coated wire is generally filled in the form of powder, so the presence of air spaces between the powders causes heat transfer resistance. big,
This is because the heat transfer from molten steel is slower than in the iron-coated area. As shown in Fig. 2, the inventor's investigation also found that the melting time was measured when the molten steel temperature was kept just above the melting point and the iron coating components of the molten steel and wire were almost the same. The melting time is determined by the wall thickness t and diameter D, and can be approximately expressed by the cross-sectional area of the iron coating as shown in FIG. From the above, in order to clarify the factors that determine the melting time of iron-coated wire and further clarify the relationship between these factors and the melting position L in practical use, we conducted an actual composite material manufacture and calculated the equation as shown in equation (4). Finally, we obtained a formula that serves as an index for controlling the melting of iron-coated wire. L=C3・ρs・S・VW ...(4) Here, L is the melting position (m), ρs is the density of the wire coating (Kg/ m3 ), and VW is the wire feeding speed ( m/min), S is the cross-sectional area of the iron-coated wire (m 2 ),
C3 is a coefficient of about 0.3 to 0.6. S is the inner diameter Di (m) and outer diameter D O (m) of the iron-coated wire
It can be found using the following formula. S=π/4・(D O 2D i 2 ) ...(5) Equation (4) is an equation based on the idea that the melting position L is controlled by the heat capacity of the wire that supplies it, and the coefficient is Since the coefficient varies somewhat depending on the temperature of the molten steel and mold size, the wire feeding speed may be controlled by selecting the most appropriate coefficient within the above range. Here, the cross-sectional shape of the iron-coated wire can be determined by treating the cross-sectional area S of the iron-coated wire in the same manner according to each shape, whether it is circular as described above, oval, square, or other shapes (4) You may apply Eq. The method for adjusting the melting position L using the iron-coated wire has been outlined above. Next, a method for adjusting and supplying alloying elements to the core portion will be described. The cross-sectional area of the molten steel in the solidified shell of the slab at the wire melting position is A (m 2 ), the density of the molten steel is ρ M (Kg/m 3 ), and the target concentration difference (increase) of alloy addition to the core is ΔC ( %),
The inner diameter of the wire is D i (m), the packing density of the alloying element in the wire is ρc (Kg/m 3 ), and the addition yield of the alloying element is η
(%), and the number of wires to be melted is N.
The material balance equation (6) is found. A × V C × ρ M × ΔC = π/4・D i 2 × ρc × V W × η × N ... (6) Here, the alloy addition amount Q supplied by the wire
is Q=π/4・D i 2 ×ρc×V W ×N (7), so the operating factor of the iron-coated wire can be expressed as follows. D i 2 V W = Q (ρc・π/4・N) ……(8) From the above, the desired amount of alloy Q is added to the core of the iron while satisfying the desired melting position L (surface layer thickness L S ). The coated wire conditions are obtained by combining the thickness, diameter, feeding speed, etc. of the iron coated wire that satisfies formulas (4) and (8). Using the above method, we have demonstrated the concept of a method for controlling the melting position of wire in the manufacture of composite materials using the core addition method. Using the method described above, it is possible to determine the necessary melting position of the wire and the outline of the wire specifications when manufacturing composite materials, but the wire melting position must be determined by taking into account the flow state of the molten steel in the mold, which is the issue mentioned above. The next point to be made is to define the conditions for determining whether the above is sufficient, and the details are described below. When the wire is melted in part A in the mold shown in FIG. 1, mixing and diffusion of the additive alloy becomes a problem in manufacturing the composite material. Regarding this point, Figure 4 shows the investigation results of the upward circulation flow in the mold through water model tests. As a standard, it is approximately (1 to 2) times the width of the long side of the mold. Therefore, mixing of the additive alloy into part A in the mold,
To prevent diffusion, the melting position L of the wire must be
(m) needs to be the following formula. L>(C1×H+L N )÷1000...(9) Here, H is the long side width of the mold size (m), L N is the immersion depth of the nozzle (mm), and C1 is a coefficient of about 1 to 1.5. It is. Furthermore, the present inventors disclose a means for optimizing the flow in the mold by changing the discharge hole of the immersion nozzle, that is, a means for relaxing the shallowest melting position constraint defined by equation (9). (1) Rotating nozzle method The discharge hole of the immersion nozzle is placed against the inner wall of the mold.
This is a method of reducing the area A in FIG. 2 by suppressing the kinetic energy of the discharge flow from reaching the under-mold area by injecting at an angle as shown in FIG. 5a. This method is particularly effective when the mold size is large. (2) Straightening of the immersion nozzle In addition to the conventional discharge hole facing the inner wall of the mold, a new discharge hole is provided below the mold at the bottom of the immersion nozzle as shown in Fig. 5b. It is characterized by supplying the amount of hot water for forming the thickness of the surface layer with as little kinetic energy as possible, and further ensuring the amount of hot water for forming the core at the latter discharge hole and the stirring energy for uniformly dispersing the added alloy. This method is particularly effective when the mold size is small. The above describes the regulations regarding the required shallowest depth for the melting position of iron-coated wire in the production of composite materials, and methods for relaxing the constraints. Next, we will discuss the maximum depth limit from the perspective of the melting position of iron-coated wire. The maximum depth limit is determined from the problem of residual metal adhering to the iron-coated wire, and is the position where the molten steel at the lower end of area B in Figure 1 has lost its heating degree ΔT (=molten steel temperature - melting point) and fluidity. It is defined. This condition is approximately determined by the decrease in the temperature of the molten steel in the mold due to heat removal due to the growth of the solidified shell relative to the heat capacity of the mold. The second term on the left side of equation (10) is an expression that defines the solidification rate in the mold, and the left side expresses the unsolidified rate (%) in the mold. Based on actual hot water tests, etc., we find the conditions under which no metal remains attached to the iron-coated wire, and it is necessary to complete melting when the unsolidified rate of the slab at the molten steel position L of the wire is 40 to 50% or more. be. 1-K・(L/V C ) 1/2・2(H+B)/(H×B)
>0.4~0.5...(10) Here, K is the solidification coefficient (mm/min 1/2 ), L is the melting position of the iron-coated wire (m), V C is the casting speed (m/min), H
is the width of the long side of the mold (mm), B is the thickness of the short side of the mold (mm)
represents. From equation (10), the maximum depth L from the melting point at the melting point is determined by the following equation. L<W C・((0.5~0.6)×(H×B)/K・2(H+B
)) 2 ...(11) To summarize the above, the shallowest depth from the melting surface of the iron-covered wire from the melting point is defined by formula (9), and the critical maximum depth L is determined by formula (11). By specifying C1 as 1 to 1.5, the melting position of iron-coated wire is
C2 is set to 0.5 to 0.6 and defined by equation (12). C1×H×LN/1000<L<V C・(C2×(H×B)/K×2
(H+B)) 2 ...(12) Effects The present invention describes the melting position control of an iron-coated wire filled with an additional alloying element. The second effect is to clarify the control range of the melting position of the wire, and the second effect is to control the melting position within the above control range by using the dimensions and feeding speed of the iron-coated wire as control factors, and to apply the wire to the core as required. The aim is to clarify the method of supplying alloying elements according to the requirements. By controlling the melting position of the iron-coated wire according to the present invention, it is possible to manufacture a good composite material. Examples Examples of continuous casting of sulfur free-cutting steel having a high core sulfur concentration will be described below. 0.06%C, 0.02%Si, 0.50%Mn, 0.025 in converter
Molten steel with a composition system of %P, 0.02%S, and 0.015%Al is melted, and a billet with a cross-sectional size of 162mm x 162mm is produced using a curved continuous machine with a curvature radius of 12m using a 5-hole immersion nozzle (4 horizontal holes). (having one vertical discharge hole) at a casting speed V C =1.8 to 2.0 m/min. A wire feed guide was installed above the mold, and casting was performed using a wire feeder to continuously feed an iron-coated wire filled with powdered sulfur into the mold from between the mold and the immersion nozzle. A steel grain with a core sulfur concentration of 0.150 to 0.250%S
Two types of sulfur-filled wires are prepared to manufacture B steel main body with 0.050 to 0.100% S, and the outer diameter for A steel type is
6.5mmφ, iron coating thickness 0.9mm, outer diameter 4.5mm for B steel type
φ, iron coating thickness was 1.0 mm. The target thickness of the surface layer of the slab without adding sulfur was 10 to 25 mm for all steel types. Table 1 shows the manufacturing conditions for the above-mentioned sulfur free-cutting steel, the measurement results of the surface layer thickness in a cross-sectional sample taken from the obtained billet slab, the analysis results of the sulfur concentration in the core, and the residual metal content in the core. Observation results regarding the presence or absence of sulfur and the presence or absence of local concentration of sulfur are shown. FIG. 6 shows the melting position of the wire calculated from the surface layer thickness after solidification with respect to the plunge speed of the iron-coated wire. Here, a specific application method of the present invention will be described in detail in association with the above embodiment. Here, as a basic condition, for the slab size,
In order to secure a surface layer thickness of 15 to 20 mm at V C = 1.8 m/min and solidification coefficient K = 24 mm/min 1/2 , from equation (1), the wire melting position should be set at 0.7 to 1.25 mm from the melt surface in the slab.
The depth must be m. On the other hand, in equation (12), which defines the conditions for separating the two molten steel pools in the slab and the conditions for complete melting of the wire, in order to produce a good composite material, the left side is given when the nozzle immersion depth is 0.2 m. (0.36 to 0.44) m, and the right side is in the range of (1.28 to 1.80) m, so if the melting position of the wire is controlled to the depth of 0.7 to 1.25 m, it is likely that the desired composite material will be obtained. Next, the wire dimensions and wire supply speed that can supply the target concentration to the core portion while controlling the melting position as described above are determined. Now, the core part starts from 0.050%S.
The required amount of sulfur to increase to 0.200%S is
0.42Kg/min and the density of sulfur is 2000Kg/m 3 by combining equation (8) for the mass balance and equations (4) and (5) for controlling the melting position of the iron-coated wire. The outer diameter D O = 6.5 mmφ, the iron coating thickness 0.9 mm, the wire feeding speed V W = 10.7 m/min, and the iron coating feeding speed 2.6 kg/min are determined. This feeding rate allows control to the melting position shown in FIG. 6, where the composite material can be stably produced. A similar method can be applied to cases where casting conditions are different.

【表】 発明の効果 以上説明したように、本発明によれば、鉄被覆
合金ワイヤーの鋳型内添加により、複合鋼材の連
続鋳造が可能となり、従来造塊法で鋳造していた
複合鋼材の製造コストの低減や品質の安定化に対
する効果は極めて大きい。
[Table] Effects of the Invention As explained above, according to the present invention, continuous casting of composite steel materials is possible by adding iron-coated alloy wire in the mold, and manufacturing of composite steel materials that was conventionally cast by the ingot method is now possible. The effects on cost reduction and quality stabilization are extremely large.

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

第1図は縦断面図、第2図は鉄被覆厚みとワイ
ヤー溶解時間の関係を示す図、第3図は鉄被覆断
面積とワイヤー溶解時間の関係を示す図、第4図
は鋳型内の上昇循環流の調査結果を示す図、第5
図a,bは鋳型内流動の最適化を計る手段の説明
図、第6図はワイヤーの投入速度と溶解位置を示
す図である。 1……ノズル、2……吐出口、3……ワイヤ
ー、4……表層部、5……コア層。
Figure 1 is a longitudinal cross-sectional view, Figure 2 is a diagram showing the relationship between iron coating thickness and wire melting time, Figure 3 is a diagram showing the relationship between iron coating cross-sectional area and wire melting time, and Figure 4 is a diagram showing the relationship between iron coating thickness and wire melting time. Figure 5 showing the survey results of upward circulation flow.
Figures a and b are explanatory diagrams of means for optimizing the flow within the mold, and Figure 6 is a diagram showing the feeding speed and melting position of the wire. 1... Nozzle, 2... Discharge port, 3... Wire, 4... Surface layer portion, 5... Core layer.

Claims (1)

【特許請求の範囲】 1 鋼の連続鋳造において、タンデイツシユから
供給された溶鋼が、母溶鋼成分の表層部(リム
層)を形成し、さらに、未凝固部への合金添加に
より、母溶鋼と異なる成分の内部(コア層)を形
成する鋳込み複合鋼材製造方法において、湯面か
らの距離で表す鉄被覆ワイヤーの溶解位置Lを、
上記鋳片表層部に添加合金が混合しないよう下式
の左辺の規定以上とし、かつ鉄被覆ワイヤーが未
溶解で鋳片内に残存しない下式の右辺の規定以下
に制御することを特徴とする鋳込み複合鋼材の製
造方法。 LN+CI×H/1000<L<Vc・(C2・(H×B)/K・2
(H+B))2 ここで、 L:鉄被覆合金ワイヤーの溶解位置の鋳型湯面か
らの距離(m) LN:浸漬ノズルの吐出孔の鋳型湯面からの距離
(mm) H:鋳型の長辺幅(mm)、B:鋳型の短辺厚み
(mm) Vc:鋳造速度(m/min)、K:凝固係数(mm/
min1/2) Cl:係数(1〜1.5)、C2:係数(0.5〜0.6) 2 請求項1の範囲内に鉄被覆合金ワイヤーの溶
解位置をコントロールする手段として、溶解位置
Lが下式に示すとおりワイヤー被覆部の投入重量
速度に比例するとした近似制御方法を特徴とする
鋳込み複合鋼材の製造方法。 L=C3・ρs・S・Vw ここで、 ρs:ワイヤー被覆部の密度(Kg/m3)、 S:ワイヤー被覆部の横断面積(m2) =π/4・(DO 2−Di 2) DO:被覆ワイヤーの外径(m)、 Di:被覆ワイヤーの内径(m) Vw:鉄被覆ワイヤーの投入速度(m/min)、 C3:係数(0.3〜0.6) 3 請求項1、2を満足し、かつ、所要合金添加
量を得るための物質収支式としての下式を制御条
件のひとつに加えることで、最終的にワイヤー条
件、投入条件を決定し、所望のコア成分を任意に
選択することを特徴とする鋳込み複合鋼材の製造
方法。 Di 2Vw=Q/N・π/4・ρc ここで、 Di:鉄被覆ワイヤーの内径(m) N:投入ワイヤー本数 Vw:鉄被覆ワイヤーの投入速度(m/min) Q:合金添加量(Kg/min) ρc:合金の充填密度(Kg/m3) 4 鋳型内での溶鋼の上昇循環流を抑制し、添加
合金の均一分散化を促進させる、あるいは/およ
び、よりリム層の薄い複合鋼材を得るために、浸
漬ノズルの吐出孔を鋳型内壁面に対して傾斜する
こと(回転流利用)、または、浸漬ノズル底部に
吐出孔を設けて下向きに吐出させること(下降流
利用)を特徴とする請求項1〜3記載の鋳込み複
合鋼材の製造方法。
[Claims] 1. In continuous casting of steel, the molten steel supplied from the tandate forms a surface layer (rim layer) of the mother molten steel, and furthermore, by adding alloy to the unsolidified portion, the molten steel is different from the mother molten steel. In a cast composite steel production method that forms the inside of the component (core layer), the melting position L of the iron-coated wire expressed as the distance from the hot water surface is
It is characterized by controlling the additive alloy to be above the specification on the left side of the equation below so that it does not mix into the surface layer of the slab, and below the specification on the right side of the equation below so that the iron-coated wire does not remain unmelted in the slab. Method for manufacturing cast composite steel materials. L N +CI×H/1000<L<Vc・(C2・(H×B)/K・2
(H+B)) 2Where , L: Distance from the mold surface to the melting position of the iron-coated alloy wire (m) L N : Distance from the mold surface to the discharge hole of the immersion nozzle (mm) H: Length of the mold Side width (mm), B: Short side thickness of mold (mm) Vc: Casting speed (m/min), K: Solidification coefficient (mm/
min 1/2 ) Cl: coefficient (1 to 1.5), C2: coefficient (0.5 to 0.6) 2 As a means of controlling the melting position of the iron-coated alloy wire within the range of claim 1, the melting position L is determined by the following formula. As shown, a method for producing a cast composite steel material is characterized by an approximate control method in which the speed is proportional to the input weight speed of the wire coating. L=C3・ρs・S・V wwhere , ρs: Density of wire coating (Kg/m 3 ), S: Cross-sectional area of wire coating (m 2 ) = π/4・(D O 2 −D i 2 ) D O : Outer diameter of coated wire (m), D i : Inner diameter of coated wire (m) V w : Feeding speed of iron coated wire (m/min), C3: Coefficient (0.3 to 0.6) 3 Claim By adding the following equation as a material balance equation to one of the control conditions to satisfy terms 1 and 2 and obtain the required amount of alloy addition, the wire conditions and charging conditions are finally determined, and the desired core is obtained. A method for manufacturing a cast composite steel material, characterized in that components are arbitrarily selected. D i 2 V w =Q/N・π/4・ρc Here, D i : Inner diameter of iron-coated wire (m) N: Number of wires V w : Feed-in speed of iron-coated wire (m/min) Q: Alloy addition amount (Kg/min) ρc: Alloy packing density (Kg/m 3 ) 4 Suppresses the upward circulation flow of molten steel in the mold, promotes uniform dispersion of the added alloy, and/or improves the rim In order to obtain a composite steel material with a thin layer, the discharge hole of the immersion nozzle is inclined with respect to the inner wall surface of the mold (rotary flow), or the discharge hole is provided at the bottom of the immersion nozzle and the discharge is directed downward (downward flow). The method for manufacturing a cast composite steel material according to claims 1 to 3, characterized in that:
JP23694789A 1989-09-14 1989-09-14 Manufacture of cast complex steel material Granted JPH0399751A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23694789A JPH0399751A (en) 1989-09-14 1989-09-14 Manufacture of cast complex steel material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23694789A JPH0399751A (en) 1989-09-14 1989-09-14 Manufacture of cast complex steel material

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Publication Number Publication Date
JPH0399751A JPH0399751A (en) 1991-04-24
JPH0573504B2 true JPH0573504B2 (en) 1993-10-14

Family

ID=17008112

Family Applications (1)

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JP23694789A Granted JPH0399751A (en) 1989-09-14 1989-09-14 Manufacture of cast complex steel material

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Country Link
JP (1) JPH0399751A (en)

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Publication number Priority date Publication date Assignee Title
JP4765774B2 (en) * 2006-05-29 2011-09-07 住友金属工業株式会社 Continuous casting method for multi-layer slabs

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