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JP6500630B2 - Continuous casting method for molten steel and continuous cast slab - Google Patents
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JP6500630B2 - Continuous casting method for molten steel and continuous cast slab - Google Patents

Continuous casting method for molten steel and continuous cast slab Download PDF

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JP6500630B2
JP6500630B2 JP2015123751A JP2015123751A JP6500630B2 JP 6500630 B2 JP6500630 B2 JP 6500630B2 JP 2015123751 A JP2015123751 A JP 2015123751A JP 2015123751 A JP2015123751 A JP 2015123751A JP 6500630 B2 JP6500630 B2 JP 6500630B2
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笹井 勝浩
勝浩 笹井
原田 寛
寛 原田
中島 潤二
潤二 中島
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Nippon Steel Corp
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通常の連続鋳造鋳片の横断面には、中心にポロシティや偏析を伴う最終凝固部を取り囲むように配された中心近傍の粗い粒状晶部と、粗い粒状晶部を取り囲む粗い柱状晶部とが観察される。この粗い粒状晶と柱状晶とを微細な等軸晶にし、中心偏析やミクロ偏析を大幅に軽減することができれば、例えばスラブを薄板にした際には成形加工性が顕著に優れた薄板になり、また例えば厚板にした際には低温靱性に優れた厚板となる。本発明は、この粗い粒状晶と柱状晶を微細な等軸晶にできる溶鋼の連続鋳造方法およびそれを用いて鋳造した微細な凝固組織を有する連続鋳造鋳片に関するものである。   In the cross section of a normal continuous casting slab, coarse granular crystal parts near the center and coarse columnar crystal parts surrounding the coarse granular crystal parts are disposed so as to surround the final solidified part with porosity and segregation at the center. It is observed. If this coarse granular crystal and columnar crystal can be made fine equiaxed and central segregation and microsegregation can be significantly reduced, for example, when the slab is made into a thin plate, it becomes a thin plate with remarkably excellent formability. Also, for example, when a thick plate is used, it becomes a thick plate excellent in low temperature toughness. The present invention relates to a continuous casting method of molten steel capable of forming coarse granular crystals and columnar crystals into fine equiaxed crystals, and a continuous cast slab having a fine solidified structure cast using the same.

非特許文献1には、等軸晶は溶鋼過熱度が低いと増加することから、等軸晶化には低温鋳造が有効であることが示されている。また、特許文献1には、誘導電磁攪拌装置を用いて、凝固界面近傍の溶鋼に一方向の旋回流を与え、柱状デンドライトを分断することにより柱状晶を等軸晶にする技術が記載されている。さらに、特許文献2には、タンディッシュ内でプラズマ加熱装置を用いて等軸晶化促進剤(Ceの酸化物、硫化物等)を溶鋼表面に吹き付け、鋳型内で等軸晶核を多数生成させることにより、鋳片中心近傍の粗い粒状晶を微細化する技術が開示されている。   Non-Patent Document 1 shows that low-temperature casting is effective for equiaxed crystallization, since equiaxed crystals increase as the degree of superheat of molten steel is low. Further, Patent Document 1 describes a technique for giving a swirling flow in one direction to molten steel in the vicinity of a solidification interface using an induction electromagnetic stirring device, and dividing columnar dendrites into equiaxed columnar crystals. There is. Furthermore, Patent Document 2 sprays an equiaxed crystallization accelerator (such as oxides and sulfides of Ce) on the surface of molten steel using a plasma heating device in a tundish to generate a large number of equiaxed nuclei in a mold. There is disclosed a technique of refining coarse granular crystals in the vicinity of the center of a cast slab by

特開昭50−23338号公報Japanese Patent Application Laid-Open No. 50-23338 特開2001−225153号公報JP 2001-225153 A

鉄鋼便覧第3版、II 製銑・製鋼、p.653Steel Manual 3rd Edition, II Steelmaking & Steelmaking, p. 653

しかしながら、低温鋳造では、溶融金属の過熱度を液相線に近い温度にし、これを浸漬ノズルから鋳型内に注入する必要があるため、浸漬ノズルの閉塞や鋳型内でのディッケル生成等の凝固異常を招く場合がある。このため、現状の連続鋳造では注入する溶融金属の過熱度は20〜30K程度を採用しており、このような温度条件では近年軽量化ニーズで生産量が増加してきている高強度薄鋼板の成形加工性や高強度厚板の低温靱性を改善できる程の微細等軸晶化は達成されていない。また、誘導電磁攪拌を用いる方法や等軸晶化促進剤を添加する方法についても、高強度鋼の材質が改善できるまでの十分な微細等軸晶が安定して得られているわけではなく、例えば等軸晶が生成し難いC含有率が0.1%以下の溶鋼に対しては、鋳片表層部の柱状晶を十分に等軸晶化することは難しい。   However, in low temperature casting, it is necessary to make the degree of superheat of the molten metal close to the liquidus and inject it into the mold from the immersion nozzle, so solidification defects such as clogging of the immersion nozzle and deckle formation in the mold May lead to For this reason, in the current continuous casting, the superheat degree of the molten metal to be injected adopts about 20 to 30 K, and under such temperature conditions, the formation of high strength thin steel plate whose production amount has been increasing due to weight reduction needs in recent years Micro equiaxed crystallization to such an extent that the processability and the low temperature toughness of a high strength thick plate can be improved has not been achieved. In addition, in the method using induction electromagnetic stirring or the method of adding an equiaxed crystallization accelerator, sufficient fine equiaxed crystals until the material of the high strength steel can be improved are not necessarily obtained stably, For example, in the case of a molten steel having a C content of 0.1% or less, in which equiaxed crystals are not easily generated, it is difficult to sufficiently equiaxize columnar crystals in the surface layer portion of a slab.

本発明は、このような現状を鑑み、高強度鋼用鋳片において中心近傍の粗い粒状晶とそれを取り囲む粗い柱状晶を、共に微細な等軸晶にできる連続鋳造方法、およびそれを用いて鋳造した微細な凝固組織を有する高強度鋼用連続鋳造鋳片の提供を課題としている。   In view of such a present situation, the present invention provides a continuous casting method capable of making both coarse granular crystals near the center and coarse columnar crystals surrounding it into fine equiaxed crystals in a slab for high strength steel, and using the same. It is an object of the present invention to provide a continuous cast slab for high strength steel having a fine solidified structure which has been cast.

このような状況に鑑み、中心近傍の粗い粒状晶とそれを取り囲む粗い柱状晶を、共に微細な等軸晶にできる連続鋳造方法およびそれを用いて鋳造した微細な凝固組織を有する連続鋳造鋳片を提供するために、凝固組織微細化元素の解明、少量添加で効果を発揮する添加方法や添加場所に関して鋭意研究を重ね、得られた知見を連続鋳造工程の中で最適に組み合わせてプロセス設計することで本発明の完成に至った。   In view of such a situation, a continuous casting method capable of making coarse granular crystals near the center and coarse columnar crystals surrounding them both into fine equiaxed crystals and a continuous cast slab having a fine solidified structure cast using the same Elucidating the solidification structure refining element, providing intensive research on the addition method and addition location that exerts the effect by small amount addition, in order to provide the process design combining the findings obtained optimally in the continuous casting process This led to the completion of the present invention.

その要旨は以下の通りである。すなわち、
(1)鋳型内メニスカス〜鋳型下10mの間に誘導電磁攪拌装置を有する連続鋳造装置を用いて、C:0.03〜0.20質量%、Si:0.08〜1.5質量%、Mn:0.5〜3.0質量%、P:0.05質量%以下、S:0.002質量%以上、N:0.0005〜0.01質量%、Nb:0.2質量%以下、V:0.2質量%以下、Mo:0.5質量%以下、酸可溶Al:0.03質量%以下、酸可溶Ti:0.1質量%未満、Ce、La、NdもしくはPrの内、少なくとも1種以上の合計:0.0003〜0.02質量%を含有し、残部がFeおよび不可避的不純物からなる溶鋼を鋳型内に注入し、該鋳型内溶鋼にBiおよびSnの内から1種以上を合計で溶鋼中含有量が0.0005〜0.01質量%になるように添加せしめ、該誘導電磁攪拌装置により水平面内で溶鋼を旋回させながら鋳造することを特徴とする連続鋳造方法。
(2)BiおよびSnの内から1種以上を含有する金属ワイヤーを鋳型内溶鋼中に連続的に供給することを特徴とする上記(1)記載の連続鋳造方法。
(3)BiおよびSnの内から1種以上を含有するモールドフラックスを鋳型内溶鋼表面上に供給することを特徴とする上記(1)記載の連続鋳造方法。
(4)誘導電磁攪拌による溶鋼の旋回流速を、鋳片の幅方向中央部の固液界面において25〜105cm/sとすることを特徴とする上記(1)〜(3)のいずれか1項記載の連続鋳造方法。
(5)上記(4)記載の連続鋳造方法により鋳片の表層から1/4厚、1/4厚から内部のそれぞれについて平均等軸晶粒径を3mm以下にしたことを特徴とする連続鋳造鋳片。
The summary is as follows. That is,
(1) C: 0.03 to 0.20% by mass, Si: 0.08 to 1.5% by mass using a continuous casting apparatus having an induction magnetic stirring device between a meniscus in a mold and 10 m below the mold Mn: 0.5 to 3.0 mass%, P: 0.05 mass% or less, S: 0.002 mass% or more, N: 0.0005 to 0.01 mass%, Nb: 0.2 mass% or less , V: 0.2% by mass or less, Mo: 0.5% by mass or less, acid-soluble Al: 0.03% by mass or less, acid-soluble Ti: less than 0.1% by mass, Ce, La, Nd or Pr In the mold, a molten steel containing a total of at least one of 0.0003 to 0.02 mass% and the balance of Fe and incidental impurities is injected into the mold, and the molten steel in the mold contains Bi and Sn. allowed added to the molten steel content is 0.0005 to 0.01 wt% of one or more in total from Continuous casting wherein the casting while swirling the molten steel in a horizontal plane by the inductive electromagnetic stirring device.
(2) The continuous casting method according to the above (1), characterized in that a metal wire containing one or more of Bi and Sn is continuously fed into molten steel in a mold.
(3) The continuous casting method according to the above (1), wherein a mold flux containing one or more of Bi and Sn is supplied onto the molten steel surface in a mold.
(4) The swirling flow velocity of the molten steel by induction electromagnetic stirring is set to 25 to 105 cm / s at the solid-liquid interface in the central portion in the width direction of the slab , any one of the above (1) to (3) The continuous casting method described.
(5) A continuous casting method characterized in that the average equiaxed grain size is 3 mm or less for each of 1⁄4 thickness and 1/4 thickness from the surface layer of the slab according to the continuous casting method described in (4) above. Slabs.

本発明によると、鋳片表層部と鋳片内部の凝固組織を、共に微細に等軸晶化した連続鋳造鋳片を製造することができるため、高強度薄鋼板では成形加工性に、高強度厚板では低温靱性に優れた材料を製造することが可能となる。   According to the present invention, since it is possible to produce a continuous cast slab in which the solidified structure of the slab surface layer portion and the inside of the slab are finely equiaxed together, the high strength thin steel plate has high formability and high strength. With a thick plate, it becomes possible to manufacture a material excellent in low temperature toughness.

Ceを0.004質量%含有させた溶鋼の連続鋳造実験における鋳片内部と鋳片表層部の平均等軸晶粒径におよぼす電磁攪拌流速の影響を示す図である。It is a figure which shows the influence of the electromagnetic stirring flow rate on the average equiaxed grain size inside the slab and the slab surface part in the continuous casting experiment of 0.004 mass% of Ce containing Ce. Ceを0.004質量%含有した溶鋼に鋳型内でBiを0.003質量%添加して連続鋳造した鋳片内部と鋳片表層部の平均等軸晶粒径におよぼす電磁攪拌流速の影響を示す図である。Influence of the electromagnetic stirring flow rate on the average equiaxed grain size inside and at the surface layer of continuously cast slab containing 0.003 mass% of Bi added to 0.004 mass% of Ce in the mold FIG.

凝固組織の形態は、凝固時の固液界面の温度勾配と凝固速度により決定され、温度勾配が小さい程、凝固速度が大きい程、等軸晶が形成され易くなる。しかし、実際の連続鋳造では鋳片表層から比較的内部まで柱状晶が成長しており、このような凝固組織形態を等軸晶主体に変える程の冷却条件の変更は難しい。そのような条件下で、凝固組織を微細等軸晶化するためには、等軸晶生成の核生成サイトを溶鋼中に分散させ、核生成頻度を上げることで微細等軸晶の形成を促進すること、界面活性効果の高い金属元素を用いて固液界面エネルギーを低下させ柱状晶自体を微細等軸晶化させる2つの方法が考えられる。本発明は、これら2つの凝固組織制御の原理を効果的に複合させ、鋳片全面に渡って凝固組織微細化効果を最大限に引き出すための制御手段を明らかにすると共に、その制御手段を連続鋳造工程の中で最適に組み合わせてプロセス設計することにより完成させたものである。本発明の基本思想は、[1]等軸晶の核生成サイトとして有効に作用する酸化物・酸硫化物を溶鋼中に微細分散させ、これに電磁攪拌を加え溶鋼の過熱度を奪うことにより鋳片内部を安定的に微細等軸晶化させると共に、[2]鋳片表層部に固液界面エネルギーを低下させる金属元素を優先的に添加して、鋳型側から鋳片内部に向かって成長する柱状晶の微細化を図り、その上で電磁攪拌の旋回流でこの微細・脆弱な柱状晶を分断することにより鋳片表層部にも微細な等軸晶を生成させることにある。その結果として、鋳片全面に渡って微細な等軸晶組織を得ることが可能となる。   The form of the solidified structure is determined by the temperature gradient and the solidification rate of the solid-liquid interface at the time of solidification, and the smaller the temperature gradient and the larger the solidification rate, the easier the equiaxed crystals are formed. However, in continuous continuous casting, columnar crystals grow from the surface layer of the slab to the inside relatively, and it is difficult to change the cooling condition so as to change the solidified structure form to equiaxed crystal as a main component. Under such conditions, in order to micro-scale the solidified structure, nucleation sites for equiaxed crystal formation are dispersed in the molten steel and nucleation frequency is increased to promote formation of micro-scaled equiaxed crystal. There are two conceivable methods of reducing the solid-liquid interface energy by using a metal element having a high surface activity effect, and micro-equiaxially crystallizing the columnar crystals themselves. The present invention effectively combines these two solidification structure control principles, reveals a control means for maximizing the solidification structure refinement effect over the entire surface of the cast slab, and continuously controls the control means. It is completed by optimally combining process design in the casting process. The basic idea of the present invention is to finely disperse in the molten steel the oxides and oxysulfides that effectively act as nucleation sites for equiaxed crystals [1] and add electromagnetic stirring to this to deprive the superheat of the molten steel. A metal element that lowers solid-liquid interface energy is preferentially added to the surface layer portion of the [2] slab while stably micro-eaxially crystallizing the inside of the slab stably, and the growth toward the inside of the slab from the mold side In order to form fine equiaxed crystals in the surface layer portion of the slab by dividing the fine and fragile columnar crystals by the swirling flow of electromagnetic stirring. As a result, it is possible to obtain a fine equiaxed crystal structure over the entire surface of the cast slab.

上記基本思想を実現するための具体的方法と条件について、以下に述べる。まず、[1]の等軸晶の核生成サイトとなる酸化物・酸硫化物の条件であるが、Ti脱酸溶鋼にはチタニア系介在物が、Al脱酸溶鋼にはアルミナ系介在物が多数存在するが、これらの介在物は極めて凝集・合体し易く粗大な酸化物となるため、等軸晶生成の核として有効に作用しない。これに対し、本発明者らは、溶鋼中にTiやAlよりも強脱酸元素であるCe、La、NdもしくはPrの内、少なくとも1種以上を添加し、チタニア系介在物およびアルミナ系介在物をCe酸化物、La酸化物、Nd酸化物、Pr酸化物、Ce酸硫化物、La酸硫化物、Nd酸硫化物、或いはPr酸硫化物に改質することにより、比較的微細な酸化物・酸硫化物を溶鋼中に均一に分散できること、これら酸化物・酸硫化物が微細な等軸晶生成の核になり易いことを見いだした。これは、チタニアやアルミナと比較して、Ce酸化物、La酸化物、Nd酸化物、Pr酸化物、Ce酸硫化物、La酸硫化物、Nd酸硫化物、或いはPr酸硫化物が溶鋼と濡れ易いためだと考えられる。ここで、Ce、La、NdもしくはPrの内、少なくとも1種以上の合計添加量は0.0003〜0.02質量%に規定した。これは、Ce、La、NdもしくはPrの内、少なくとも1種以上の合計添加量が0.0003%未満では等軸晶核生成サイトの量が少なくなることにより、反対に0.02質量%を超えると生成酸化物または酸硫化物が粗大化し易くなることにより、何れも鋳片内の凝固組織を微細な等軸晶にする効果が失われるためである。   Specific methods and conditions for realizing the above basic idea will be described below. First, the conditions for oxides and acid sulfides, which become nucleation sites for equiaxed crystals in [1], are titanium-based inclusions in Ti-deoxidized molten steel, and alumina-based inclusions in Al-deoxidized molten steel. Although many inclusions exist, these inclusions are extremely easy to aggregate and combine to form coarse oxides, and thus do not function effectively as nuclei for equiaxial crystal formation. On the other hand, the present inventors added at least one or more of Ce, La, Nd or Pr, which is a stronger deoxidizing element than Ti and Al, to molten steel, and included titania inclusions and alumina inclusions. Relatively fine oxidation by reforming the oxide into Ce oxide, La oxide, Nd oxide, Pr oxide, Ce oxysulfide, La oxysulfide, Nd oxysulfide or Pr oxysulfide It has been found that it is possible to uniformly disperse metal oxides and acid sulfides in molten steel and that these oxides and acid sulfides are likely to become nuclei of fine equiaxed crystal formation. This means that Ce oxide, La oxide, Nd oxide, Pr oxide, Ce oxysulfide, La oxysulfide, Nd oxysulfide, or Pr oxysulfide are molten steel compared to titania or alumina. It is thought that it is because it is easy to get wet. Here, the total addition amount of at least one or more kinds of Ce, La, Nd or Pr is defined to 0.0003 to 0.02 mass%. This is because, if the total addition amount of at least one or more of Ce, La, Nd or Pr is less than 0.0003%, the amount of equiaxial nucleation sites is decreased, and conversely 0.02 mass% is contained. If it exceeds, the formed oxide or oxysulfide tends to be coarsened, and in any case, the effect of making the solidified structure in the slab into fine equiaxed crystals is lost.

本発明では、溶鋼中の溶存(酸可溶)Al濃度は0.03質量%以下であり、これを超える酸可溶Al濃度ではアルミナ系介在物を完全にCe酸化物、La酸化物、Nd酸化物、Pr酸化物、Ce酸硫化物、La酸硫化物、Nd酸硫化物、或いはPr酸硫化物に改質できず、アルミナとの複合介在物となり凝集・合体が進行すると共に、等軸晶の核生成サイトとしての能力を失う。Ce酸化物、La酸化物、Nd酸化物、Pr酸化物、Ce酸硫化物、La酸硫化物、Nd酸硫化物、或いはPr酸硫化物の凝集・合体を抑制し、等軸晶の核生成能を維持するためには酸可溶Al濃度は低い方が良く、下限値は0質量%を含む。また、酸可溶Al濃度とは、酸に溶解したAl量を測定したもので、溶存Alは酸に溶解し、アルミナは酸に溶解しないことを利用した分析方法である。ここで、酸とは、例えば塩酸1、硝酸1、水2の割合で混合した混酸である。   In the present invention, the concentration of dissolved (acid-soluble) Al in molten steel is 0.03% by mass or less, and if the concentration of acid-soluble Al is more than this, alumina inclusions can be completely removed by Ce oxide, La oxide, Nd It can not be reformed into oxides, Pr oxides, Ce oxysulfides, La oxy sulfides, Nd oxy sulfides, or Pr oxy sulfides, and becomes complex inclusions with alumina, while aggregation and coalescence progress, Lose their ability as crystal nucleation sites. Suppresses the aggregation and combination of Ce oxide, La oxide, Nd oxide, Pr oxide, Ce acid sulfide, La acid sulfide, Nd acid sulfide, or Pr acid sulfide, and produces equiaxial nucleation In order to maintain the performance, the acid-soluble Al concentration should be low, and the lower limit includes 0% by mass. The acid-soluble Al concentration is a measurement of the amount of Al dissolved in an acid, which is an analysis method utilizing the fact that dissolved Al dissolves in an acid and alumina does not dissolve in an acid. Here, the acid is, for example, a mixed acid mixed in the proportion of hydrochloric acid 1, nitric acid 1 and water 2.

また、酸可溶Ti濃度も高くなり過ぎると、その酸化物が凝集合体して粗大になり易いこと、鋼中のNと結びついて粗大なTiNの介在物を生成し易いことから、酸可溶Ti濃度は0.1質量%未満とし、下限値は0質量%を含む。酸可溶Ti濃度は、酸可溶Al濃度と同様、酸に溶解したTi量を測定したもので、溶存Ti濃度に一致する。   In addition, when the acid-soluble Ti concentration is too high, the oxide is likely to aggregate and become coarse, and it is easy to form coarse TiN inclusions by being combined with N in the steel, so acid-soluble The Ti concentration is less than 0.1% by mass, and the lower limit includes 0% by mass. The acid-soluble Ti concentration, like the acid-soluble Al concentration, is obtained by measuring the amount of Ti dissolved in the acid, and corresponds to the dissolved Ti concentration.

次に、[1]の電磁攪拌の条件に関して述べる。一般に、電磁攪拌では、凝固界面の溶鋼に旋回流を付与するため、この旋回流が柱状デンドライトを分断し、等軸晶化を促進すると考えられている。しかし、本発明者等の知見では、従来から言われている鋳片表層部の凝固界面における柱状晶分断の効果は弱く、むしろ電磁攪拌により凝固シェルと溶鋼間の熱伝達が促進され、鋳片内部の溶鋼過熱度を低下させる効果が高いことを見いだした。本発明の等軸晶の核生成促進では、この電磁攪拌の溶鋼過熱度を低下させる効果を活用し、電磁攪拌により微細な酸化物・酸硫化物を起点に生成した等軸晶核の再溶解を防止している。しかしながら、電磁攪拌による溶鋼過熱度の低減効果を高めていくためには、旋回流速を速くする必要があり、その場合微細な酸化物・酸硫化物が凝集・合体により粗大化し、等軸晶の核として有効に機能しなくなる。そこで、C:0.08質量%、Si:0.5質量%、Mn:1.0質量%、P:0.02質量%、S:0.003質量%、N:0.003質量%、酸可溶Al:0.025質量%、酸可溶Ti:0.04質量%、Ce:0.004質量%の溶鋼の連続鋳造実験を実施し、鋳片内部と鋳片表層部の等軸晶粒径におよぼす電磁攪拌の旋回流速の影響を調査した。なお、分岐状柱状晶(分断されていない)、分断された柱状晶、分断された分岐状柱状晶についても、その粒径を同時に評価できるように、等軸晶粒径は2(a・b)0.5と定義した(aは結晶粒の長径、bは結晶粒の短径で
ある。分断されていない分岐状柱状晶についてはひとつの枝をひとつの結晶粒とした。)。鋳片内部の平均等軸晶粒径は、鋳片1/4厚から内部における横断面の等軸晶粒径の平均値、鋳片表層部の平均等軸晶粒径は、表層から鋳片1/4厚における横断面の等軸晶粒径の平均値である。鋳片内部と鋳片表層部における平均等軸晶粒径におよぼす電磁攪拌流速の影響を図1に示す。図1から分かるように、鋳片内部の平均等軸晶粒径は溶鋼の旋回流速が25cm/s以上で3mm以下に、30cm/s以上で2mm程度まで小さくなるが、100cm/sを超えると反対に平均等軸晶粒径は大きくなり始め、105cm/s超では3mmを超えて粗大化する。この原因は、電磁攪拌の旋回流速が25cm/s以上、より明確には30cm/s以上になると鋳片内部で微細酸化物を起点に生成した等軸晶核の再溶解が抑制されるのに対し、旋回流速が100cm/sを超えると鋳片内部でCe酸化物やCe酸硫化物でも、凝集・合体による粗大化が進行し、等軸晶の核として機能し難くなり、105cm/sを超えると等軸晶核として機能しなくなるためだと考えられる。なお、鋳片表層部については、殆どが鋳型側から鋳片内部に向かって一定方向に揃った比較的長い分岐状柱状晶が成長しており、分断されていない分岐状柱状晶、分断した分岐状柱状晶、柱状晶を含む平均等軸晶粒径は粗大であった。これは、電磁攪拌による鋳片表層部の凝固界面における柱状晶分断の効果が比較的弱いためである。したがって、鋳片内部の凝固組織を微細な等軸晶にするためには、電磁攪拌の旋回流速を30〜100cm/sに制御するのが望ましい。また、鋳型下10mよりも更に下方では、既に鋳片表層の凝固はほぼ完了しているため、誘導電磁攪拌は凝固の始まる鋳型内メニスカスの位置と鋳型下10mの位置との間に設置するのが効果的である。鋳型内あるいは鋳型直下に設置するのが更に望ましい。
Next, the conditions of the electromagnetic stirring of [1] will be described. Generally, in electromagnetic stirring, it is believed that this swirling flow breaks up the columnar dendrite to promote equiaxed crystallization because it imparts a swirling flow to the molten steel at the solidification interface. However, according to the findings of the present inventors, the effect of columnar crystal division at the solidification interface of the surface layer portion of the slab conventionally known is weak, and rather, heat transfer between the solidified shell and the molten steel is promoted by electromagnetic stirring, It was found that the effect of reducing the internal superheat of molten steel was high. In the promotion of nucleation of equiaxed crystals of the present invention, re-dissolution of equiaxed nuclei formed from fine oxides and oxysulfides as starting points by electromagnetic stirring utilizing the effect of lowering the degree of superheat of molten steel by the electromagnetic stirring. To prevent. However, in order to increase the reduction effect of the molten steel superheat degree by electromagnetic stirring, it is necessary to increase the swirling flow velocity, in which case fine oxides and oxysulfides become coarse due to aggregation and coalescence, resulting in equiaxed crystals. It does not function effectively as a nucleus. Therefore, C: 0.08 mass%, Si: 0.5 mass%, Mn: 1.0 mass%, P: 0.02 mass%, S: 0.003 mass%, N: 0.003 mass%, The continuous casting experiment of molten steel of acid soluble Al: 0.025% by mass, acid soluble Ti: 0.04% by mass, Ce: 0.004% by mass was carried out, and the equiaxed inside of the slab and the surface layer portion of the slab The influence of the swirling flow velocity of the electromagnetic stirring on the grain size was investigated. The equiaxed grain size is 2 (a · b) so that the grain sizes of branched columnar crystals (not divided), divided columnar crystals, and divided branched columnar crystals can be simultaneously evaluated. It defined as 0.5 (a is a major axis of a crystal grain, b is a minor axis of a crystal grain. One branch is made into one crystal grain about a branched columnar crystal which is not divided). The average equiaxed grain size inside the slab, the average value of the equiaxed grain size in the cross section from the 1/4 thickness of the slab inside, and the average equiaxed grain size in the surface layer of the slab from the surface layer to the slab It is the average value of the equiaxed grain size of the cross section in 1/4 thickness. The effect of the electromagnetic stirring flow rate on the average equiaxed grain size in the inside of the slab and in the surface layer of the slab is shown in FIG. As can be seen from FIG. 1, the average equiaxed grain size inside the cast slab decreases to about 2 mm at 30 cm / s or more when the swirling velocity of the molten steel is 25 cm / s or more and 3 mm or less, but exceeds 100 cm / s On the contrary, the average equiaxed grain size starts to increase, and when it exceeds 105 cm / s, it coarsens over 3 mm. The reason for this is that if the swirling flow rate of the electromagnetic stirring is 25 cm / s or more, more specifically 30 cm / s or more, re-dissolution of equiaxed crystal nuclei generated from the fine oxide inside the slab is suppressed. On the other hand, when the swirling flow velocity exceeds 100 cm / s, coarsening by aggregation and coalescence progresses even in Ce oxide or Ce oxysulfide inside the slab, and it becomes difficult to function as an equiaxed crystal nucleus, and 105 cm / s If it exceeds, it is considered that it does not function as an equiaxed crystal nucleus. In the surface layer portion of the slab, relatively long branched columnar crystals that are aligned almost in a fixed direction from the mold side toward the inside of the slab are grown, and are not divided branch columnar crystals, divided branches The average equiaxed grain size including columnar crystals and columnar crystals was coarse. This is because the effect of columnar crystal division at the solidification interface of the surface layer portion of the slab by electromagnetic stirring is relatively weak. Therefore, in order to make the solidified structure inside the cast slab into fine equiaxed crystals, it is desirable to control the swirling flow rate of the electromagnetic stirring to 30 to 100 cm / s. In addition, since solidification of the surface layer of the slab is almost complete below 10m below the mold, induction electromagnetic stirring is placed between the position of the meniscus in the mold where solidification starts and the position of 10m below the mold Is effective. It is more desirable to set in the mold or just under the mold.

次に、[2]固液界面エネルギーを低下させる金属元素の選定であるが、鋼板材質に悪影響を与えることなく少量添加で界面活性効果が得られる元素としてBiおよびSnが有望であることを、これら金属元素を添加した10kg溶鋼の凝固実験で柱状晶間隔を評価することにより見いだした。柱状晶微細化の効果は、これら金属元素の内から1種以上を合計で0.0005質量%以上添加すれば十分であるが、0.01質量%を超えて添加すると鋼板が脆化し圧延時に端部に耳割れが発生した。このため、溶鋼中にはBiおよびSnの内から1種以上を合計で0.0005〜0.01質量%になるように添加すればよい。さらに、BiおよびSnの添加場所は鋳片材質全体に悪影響を与え難く、なるべく鋳片表層部で柱状晶微細化の効果のみを最大限に享受できるように、鋳型内の溶鋼中に添加するのが望ましい。添加方法としては、BiおよびSnを含有する金属ワイヤーを直接鋳型内の溶鋼上部側に挿入するか、或いはBiおよびSnを含有するモールドフラックスを用いて供給することで、比較的鋳片表層部に効率的に添加できる。モールドフラックスを介して微細化元素を添加する方法としては、事前にBiやSnを混入させたモールドフラックスを使用する方法、添加直前にBiやSnをモールドフラックスに混入させながら鋳型内に供給する方法、鋳造中に一定の速度でBi粉やSn粉を湯面被覆しているモールドフラックス上に供給する方法、などが有効である。BiおよびSnの沸点は各々1560℃と2270℃であり、溶鋼の融点(純鉄1538℃)よりも高いため添加時に爆発的なガス化は生じない。さらに、BiとSnの密度は各々9.8g/cm3と7.3g/cm3であり、溶鋼の密度7.0g/cm3よりも重いことから、ワイヤーやパウダーから溶鋼表面
に添加しても直ちに浮上してしまうことはなく、溶鋼中に比較的容易に添加できる。添加したBi、Snの含有量については、スラブ又は圧延鋼板から採取した試料の分析によって評価することができる。
Next, [2] is the selection of metal elements that lower the solid-liquid interface energy, but Bi and Sn are promising as elements that can obtain the surface activity effect by adding a small amount without adversely affecting the steel sheet material, It was found by evaluating the spacing between columnar crystals in a solidification experiment of 10 kg molten steel to which these metal elements were added. It is sufficient to add 0.0005% by mass or more in total of one or more of these metal elements for the effect of refining the columnar crystals, but if it is added in excess of 0.01% by mass, the steel plate becomes brittle and is rolled. Ear cracking occurred at the end. Therefore, one or more of Bi and Sn may be added to the molten steel in a total amount of 0.0005 to 0.01% by mass. Furthermore, the locations where Bi and Sn are added are unlikely to adversely affect the entire material of the slab, and are preferably added to the molten steel in the mold so that only the effect of columnar grain refinement can be maximized at the surface layer portion of the slab. Is desirable. As a method of addition, the metal wire containing Bi and Sn is directly inserted into the upper part of the molten steel in the mold, or supplied using a mold flux containing Bi and Sn, relatively to the surface layer of the slab. It can be added efficiently. As a method of adding the refining element through the mold flux, a method of using a mold flux mixed with Bi or Sn in advance, a method of supplying Bi or Sn into the mold flux while mixing it into the mold flux just before the addition A method of supplying Bi powder or Sn powder onto a mold flux which is coated at a constant speed during casting is effective. The boiling points of Bi and Sn are 1560 ° C. and 2270 ° C., respectively, and are higher than the melting point of liquid steel (pure iron 1538 ° C.), so explosive gasification does not occur upon addition. Furthermore, the density of Bi and Sn are each 9.8 g / cm 3 and 7.3 g / cm 3, since heavier than the density 7.0 g / cm 3 of the molten steel, is added to the molten steel surface from a wire or powder Also, it does not immediately rise and can be added relatively easily into molten steel. The content of added Bi and Sn can be evaluated by analysis of a sample collected from a slab or a rolled steel sheet.

さらに、[2]の電磁攪拌の条件について述べる。ここでは、先に述べたように凝固界面における電磁攪拌の柱状晶分断効果が弱いことから、鋳型内にBiおよびSnを添加して、鋳型側から成長する柱状晶を微細・脆弱化させ、この柱状晶を電磁攪拌の弱い剪断力により効果的に分断し、鋳片表層部に微細な等軸晶を造り込むことが重要となる。そこで、C:0.08質量%、Si:0.5質量%、Mn:1.0質量%、P:0.02質量%、S:0.003質量%、N:0.003質量%、酸可溶Al:0.025質量%、酸可溶Ti:0.04質量%、Ce:0.004質量%の溶鋼を鋳型内に注入し、鋳型内で連鋳パウダーを通してBiを0.003質量%添加しながら連続鋳造する実験を実施し、鋳片内部と鋳片表層部の平均等軸晶粒径におよぼす電磁攪拌の旋回流速の影響を調査し、図2に示す。鋳片表層部の平均等軸晶粒径は、電磁攪拌による旋回流速が25cm/s以上になると3mm以下まで、旋回流速が30cm/s以上になると2mm程度まで小さくなり、さらに旋回流速が100cm/s超でもその効果は維持されている。これは、電磁攪拌の旋回流速が25cm/s以上になると、鋳型内でのBi添加により微細・脆弱化された柱状晶が電磁攪拌流により分断されはじめ、さらに30cm/s以上になるとより効果的に柱状晶の分断効果が得られ、鋳片表層部に微細等軸晶を生成できることを示す結果である。一方、図2から分かるように、溶鋼の旋回流速が30cm/s以上になると鋳片内部の平均等軸晶粒径は2mm程度まで小さくなるが、100cm/sを超えると反対に平均等軸晶粒径は大きくなり始める。この原因は、先の実験でも述べたように、電磁攪拌の旋回流速が30cm/s以上になると鋳片内部で微細なCe酸化物やCe酸硫化物を起点に生成した等軸晶核の再溶解が効果的に抑制されるのに対し、旋回流速が100cm/sを超えると鋳片内部でCe酸化物やCe酸硫化物でも、凝集・合体による粗大化が始まり、等軸晶の核として機能し難くなるためだと考えられる。したがって、鋳片全体を微細等軸晶化するには、電磁攪拌流速を30〜100cm/sとすることが効果的である。   Furthermore, the conditions of electromagnetic stirring of [2] will be described. Here, since the columnar crystal division effect of electromagnetic stirring at the solidification interface is weak as described above, Bi and Sn are added in the mold to make the columnar crystals grown from the mold side fine and weaken, It is important to divide the columnar crystals effectively by the weak shear force of electromagnetic stirring and to form fine equiaxed crystals in the surface layer of the slab. Therefore, C: 0.08 mass%, Si: 0.5 mass%, Mn: 1.0 mass%, P: 0.02 mass%, S: 0.003 mass%, N: 0.003 mass%, Molten steel with 0.025% by mass of acid-soluble Al, 0.04% by mass of acid-soluble Ti, 0.004% by mass of Ce: 0.004% by mass is poured into a mold, and Bi is continuously cast in the mold through 0.003 of continuous cast powder. An experiment was conducted to carry out continuous casting while adding mass%, and the influence of the swirling flow velocity of electromagnetic stirring on the average equiaxed grain size of the inside of the slab and the surface layer portion of the slab was investigated, and is shown in FIG. The average equiaxed grain size of the surface layer of the slab decreases to 3 mm or less when the swirling flow velocity by electromagnetic stirring is 25 cm / s or more, and to about 2 mm when the swirling flow velocity is 30 cm / s or more. The effect is maintained even over s. This is more effective when the swirling flow rate of the magnetic stirring becomes 25 cm / s or more, and the columnar crystals finely divided and embrittled by the addition of Bi in the mold begin to be divided by the magnetic stirring flow, and become 30 cm / s or more. These results show that the effect of dividing columnar crystals is obtained, and fine equiaxed crystals can be generated in the surface layer portion of the slab. On the other hand, as can be seen from FIG. 2, the average equiaxed grain size inside the slab decreases to about 2 mm when the turning flow velocity of molten steel is 30 cm / s or more, but when it exceeds 100 cm / s, the average equiaxed The particle size starts to grow. The cause of this is, as described in the previous experiment, that when the swirling velocity of the electromagnetic stirring is 30 cm / s or more, re-generation of equiaxed nuclei formed from fine Ce oxide and Ce oxysulfide inside the slab. While dissolution is effectively suppressed, when the swirling flow velocity exceeds 100 cm / s, coarsening due to aggregation and coalescence begins even with Ce oxide or Ce oxysulfide inside the slab, and it becomes an equiaxed crystal nucleus It is thought that it becomes difficult to function. Therefore, in order to micro-equiaxially crystallize the entire slab, it is effective to set the electromagnetic stirring flow rate to 30 to 100 cm / s.

電磁攪拌流速については、柱状晶や分岐状柱状晶組織が発達する通常の連続鋳造条件において、鋳造した鋳片の幅方向中央部の凝固組織をピクリン酸エッチングで現出し、柱状晶や分岐状柱状晶の傾きから流速を評価することができる。この方法によって予め電磁攪拌推力と電磁攪拌流速の関係を求めておき、本発明方法においても、目標とする電磁攪拌流速を得るための電磁攪拌推力を選択して電磁攪拌を実施すればよい。   With regard to the electromagnetic stirring flow rate, under normal continuous casting conditions in which columnar crystals and branched columnar crystal structures develop, the solidified structure in the central portion in the width direction of the cast slab is revealed by picric acid etching. The flow velocity can be estimated from the inclination of the crystal. The relationship between the electromagnetic stirring thrust and the electromagnetic stirring flow velocity is previously obtained by this method, and in the method of the present invention, the electromagnetic stirring thrust for obtaining the target electromagnetic stirring flow velocity may be selected to carry out the electromagnetic stirring.

上記[1]と[2]の組み合わせによって、鋳片の表層から1/4厚、1/4厚から内部のそれぞれについて平均等軸晶粒径を3mm以下(電磁攪拌流速25〜105cm/s)、望ましくは2mm以下(電磁攪拌流速30〜100cm/s)の凝固組織を得ることができる。電磁撹拌流速は、更に望ましくは、70〜100cm/sである。   By the combination of the above [1] and [2], the average equiaxed grain size is 3 mm or less (electromagnetic stirring flow rate 25 to 105 cm / s) for each of 1/4 thickness and 1/4 thickness from the surface layer of the slab Preferably, a coagulated structure of 2 mm or less (magnetic stirring flow rate of 30 to 100 cm / s) can be obtained. The magnetic stirring flow rate is more preferably 70 to 100 cm / s.

本発明は、上記説明からも分かるように、スラブへの適用に限られたものではなく、ブルームやビレットに適用しても、十分な凝固組織の微細化効果が得られる。   As can be understood from the above description, the present invention is not limited to application to slabs, and even when applied to blooms and billets, a sufficient refinement effect of solidified structure can be obtained.

最後に、本発明の化学成分の限定理由について記載する。   Finally, the reasons for limitation of the chemical composition of the present invention will be described.

Cは鋼板の強度を確保するために必須の元素であり、高強度鋼板を得るためには少なくとも0.03質量%が必要である。しかし、過剰に含まれると、Ti等の添加元素によりCを固定したり、冷却条件を駆使しても、伸びフランジ特性に好ましくないセメンタイト相の生成が避けられないので0.20質量%以下とする。   C is an essential element to secure the strength of the steel plate, and at least 0.03 mass% is required to obtain a high strength steel plate. However, if it is contained excessively, even if C is fixed by an additive element such as Ti or the cooling condition is used, the formation of a cementite phase which is not preferable for the stretch flange characteristics can not be avoided, so 0.20 mass% or less Do.

Siは曲げ性の劣化を比較的抑えて、強度向上に寄与する元素であり、その効果を発揮するためには0.08質量%以上の添加が必要である。過剰に添加すると溶接性や延性に悪影響を及ぼすので1.5質量%を上限とする。   Si is an element which contributes to strength improvement by relatively suppressing deterioration of bendability, and addition of 0.08 mass% or more is necessary to exhibit the effect. Excessive addition adversely affects weldability and ductility, so the upper limit is 1.5% by mass.

MnはC、Siとともに鋼板の高強度化に有効な元素であり、0.5質量%以上は含有させる必要があるが、3.0質量%を超えて含有させると延性が劣化するため上限を3.0質量%とする。   Mn is an element effective for strengthening the steel sheet together with C and Si, and 0.5% by mass or more needs to be contained, but if it is contained in excess of 3.0% by mass, the ductility deteriorates, so the upper limit is made It is 3.0 mass%.

Pは固溶強化元素として有効であるが、偏析による加工性の劣化が懸念されるので0.05質量%以下にする必要がある。固溶強化の必要がなければPを添加する必要はなく、Pの下限値は0質量%を含む。   P is effective as a solid solution strengthening element, but since there is a concern about deterioration of processability due to segregation, it is necessary to make it 0.05 mass% or less. If there is no need for solid solution strengthening, it is not necessary to add P, and the lower limit value of P includes 0% by mass.

Sは、MnSの粗大な延伸介在物を形成して加工性を劣化させるため、従来はS濃度0.002質量%の極低硫化が加工性確保に必須であったが、本発明では微細で硬質なCe酸化物、La酸化物、Nd酸化物、Pr酸化物、Ce酸硫化物、La酸硫化物、Nd酸硫化物、或いはPr酸硫化物上にMnSを析出させ、圧延時にも変形が起こりにくく、介在物の延伸を防止しているため、S濃度の上限値は特に規定しない。しかしあまりS濃度が高過ぎると、MnSの変形を抑制するCe酸化物、La酸化物、Nd酸化物、Pr酸化物、Ce酸硫化物、La酸硫化物、Nd酸硫化物、或いはPr酸硫化物が多量に必要となり、それに伴いCe、La、NdもしくはPrの内、少なくとも1種以上の合計添加量が0.02質量%を超えるため、生成酸化物または酸硫化物が粗大化し易くなる不都合があり、0.02質量%以下が望ましい。また、S濃度は従来並の0.002質量%未満に低減するためには、二次精錬で脱硫処理を相当強化する必要があり、脱硫処理コストが高くなりすぎること、すなわち、本発明の副次的なMnSの形態制御の効果を享受する意義が少なくなるためS濃度の下限値は0.002質量%とする。   Since S forms coarse drawn inclusions of MnS and degrades processability, conventionally, extremely low sulfurization with an S concentration of 0.002 mass% has been essential for securing processability, but in the present invention, it is fine MnS is deposited on hard Ce oxide, La oxide, Nd oxide, Pr oxide, Ce oxysulfide, La oxysulfide, Nd oxysulfide or Pr oxysulfide, and deformation occurs even during rolling The upper limit of the S concentration is not particularly defined because it is unlikely to occur and stretching of inclusions is prevented. However, if the S concentration is too high, Ce oxide, La oxide, Nd oxide, Pr oxide, Ce oxysulfide, La oxysulfide, Nd oxysulfide, or Pr oxysulfide which suppress deformation of MnS In addition, the total amount of at least one of Ce, La, Nd, or Pr is more than 0.02% by mass, so that the resulting oxide or oxysulfide tends to coarsen. And is preferably at most 0.02 mass%. In addition, in order to reduce the S concentration to less than the conventional 0.002 mass%, it is necessary to considerably strengthen the desulfurization treatment in the secondary refining, and the desulfurization treatment cost becomes too high, that is, The lower limit value of the S concentration is set to 0.002% by mass because the significance of receiving the effect of the next form control of MnS decreases.

Nは添加し過ぎると、微量なAlであっても粗大な析出物を生成し、加工性を劣化させるので、0.01質量%を上限とする。一方、0.0005質量%未満とするにはコストがかかるので、0.0005質量%を下限とする。   When N is added too much, coarse precipitates are formed even with a slight amount of Al and the processability is degraded, so the upper limit is 0.01 mass%. On the other hand, the cost is less than 0.0005% by mass, so the lower limit is 0.0005% by mass.

Nb、Vはより高い強度を得るために添加する元素であり、これら元素と結合して形成される炭窒化物による析出強化を利用するものである。析出強化は、これら元素の単独、或いは複合添加で得られるが、過度の添加は加工性を劣化させるため、これら元素の1種または2種でそれぞれ0.2質量%を上限とする。強度向上効果を得るためには、それぞれ0.005質量%以上添加することが好ましい。   Nb and V are elements added to obtain higher strength, and use precipitation strengthening by carbonitrides formed by bonding with these elements. Precipitation strengthening is obtained by adding these elements singly or in combination, but since excessive addition deteriorates the processability, one or two of these elements have an upper limit of 0.2 mass% each. In order to obtain the strength improvement effect, it is preferable to add each in 0.005% by mass or more.

Moも強度を向上させるために用いられる元素であるが、主に焼き入れ性を高めるために添加される。過度に添加すると、延性の劣化を招くことから0.5質量%を上限とする。焼き入れ性を確保する場合には、0.05質量%以上添加することが好ましい。Nb、V、Moは含有しなくても良い。   Mo is also an element used to improve strength, but is mainly added to improve hardenability. Excessive addition causes deterioration of ductility, and the upper limit is 0.5% by mass. When securing hardenability, it is preferable to add 0.05 mass% or more. Nb, V and Mo may not be contained.

材質確保の観点から主要な添加元素は以上であるが、スクラップの利用による微量のCu、NiおよびCr等の不可避的不純物としての混入は、本発明を損なうものではない。   The main additive elements are the above from the viewpoint of securing the material, but the inclusion as unavoidable impurities such as trace amounts of Cu, Ni and Cr by utilization of scrap does not impair the present invention.

以下に、実施例及び比較例を挙げて、本発明について説明する。   The present invention will be described below with reference to examples and comparative examples.

表1のBiとSnを除く化学成分の溶鋼を溶製し、タンディッシュ内に注入した。表1のBiとSnの成分値に応じて、鋳型内の溶鋼中にBiとSnをワイヤー添加しながら鋳造した。鋳片サイズは厚み250mm×幅1500mmで、鋳造速度は1.3m/minである。誘導電磁攪拌は鋳型内メニスカスに設置されており、鋳造中はこの電磁攪拌装置に500A、周波数2Hzの電流を流して溶鋼を40cm/sで攪拌した。一部の実験(実施例18、19、20)では、電磁攪拌装置の電流を変化させ、溶鋼を90cm/s、25cm/sおよび105cm/sで攪拌した。本実験で得られた鋳片の凝固組織を調査した結果を表1に示す。本発明の実施例である試験番号1、5、9〜14、18〜21では、溶鋼中にCe、La、NdもしくはPrの内、少なくとも1種以上を含有させることにより、等軸晶の核生成サイトとして有効なCe、La、Nd、Pr酸化物・酸硫化物を溶鋼中に微細分散させ、これに電磁攪拌を加え溶鋼の過熱度を奪うことにより鋳片内部を安定的に粒径3mm以下に微細等軸晶化させると共に、鋳型内で固液界面エネルギーを低下させるBiおよびSnを優先的に添加して、鋳型側から鋳片内部に向かって成長する柱状晶の微細・脆弱化を図り、その上で電磁攪拌の旋回流でこの微細・脆弱な柱状晶を分断することにより、鋳片表層部にも粒径3mm以下の微細な等軸晶を生成させることに成功した。一方、比較例である試験番号2、6、15では鋳型内でのBiおよびSn添加を実施しなかったため鋳片表層部の分岐状柱状晶が粗大化し、比較例である試験番号3、7、16では等軸晶の核生成サイトとして有効なCe、La、Nd、およびPrを溶鋼中に含有させなかったため鋳片内部の等軸晶が粗大化し、さらに比較例である試験番号4、8、17ではCe、La、NdおよびPrの含有もなく、鋳型内でのBiおよびSn添加もなかったため、鋳片内部と表層部の何れにおいても等軸晶は粗大化した。   The molten steel of the chemical component except Bi and Sn of Table 1 was melted and poured in a tundish. According to the component value of Bi and Sn of Table 1, it casted, adding Bi and Sn in the molten steel in a casting_mold | die in a wire. The slab size is 250 mm thick × 1500 mm wide, and the casting speed is 1.3 m / min. The induction magnetic stirring was placed on the meniscus in the mold, and during casting, a current of 500 A and a frequency of 2 Hz was supplied to the magnetic stirring device to stir the molten steel at 40 cm / s. In some experiments (Examples 18, 19, 20), the current of the magnetic stirrer was varied and the molten steel was stirred at 90 cm / s, 25 cm / s and 105 cm / s. Table 1 shows the results of investigation of the solidified structure of the slab obtained in the present experiment. In Test Nos. 1, 5, 9 to 14 and 18 to 21 which are examples of the present invention, the core of equiaxed crystal is obtained by containing at least one or more of Ce, La, Nd or Pr in molten steel. Finely disperse Ce, La, Nd, Pr oxides and oxysulfides that are effective as formation sites in molten steel, adding electromagnetic stirring to this and removing the superheat of the molten steel to stabilize the inside diameter of the slab by 3 mm In addition to the following, micro-equiaxial crystallization and preferential addition of Bi and Sn, which lower the solid-liquid interface energy in the mold, make fine and weakening of columnar crystals grown from the mold side toward the inside of the slab. We succeeded in generating fine equiaxed crystals with a grain size of 3 mm or less even in the surface layer of the slab by dividing the fine and fragile columnar crystals with a swirling flow of electromagnetic stirring on top of that. On the other hand, in Test Nos. 2, 6 and 15 as Comparative Examples, Bi and Sn were not added in the mold, so branched columnar crystals in the surface layer portion of the slab became coarse, and Test Nos. 3, 7 and Comparative Examples. In No. 16 because Ce, La, Nd and Pr effective as nucleation sites for equiaxed crystals were not contained in the molten steel, the equiaxed crystals in the inside of the slab became coarser, and test numbers 4, 8 which are comparative examples, Since No. 17 contained neither Ce, La, Nd nor Pr and did not add Bi and Sn in the mold, the equiaxed crystals were coarsened in both the inside of the slab and the surface layer.

Figure 0006500630
Figure 0006500630

Claims (5)

鋳型内メニスカス〜鋳型下10mの間に誘導電磁攪拌装置を有する連続鋳造装置を用いて、C:0.03〜0.20質量%、Si:0.08〜1.5質量%、Mn:0.5〜3.0質量%、P:0.05質量%以下、S:0.002質量%以上、N:0.0005〜0.01質量%、Nb:0.2質量%以下、V:0.2質量%以下、Mo:0.5質量%以下、酸可溶Al:0.03質量%以下、酸可溶Ti:0.1質量%未満、Ce、La、NdもしくはPrの内、少なくとも1種以上の合計:0.0003〜0.02質量%を含有し、残部が鉄および不可避的不純物からなる溶鋼を鋳型内に注入し、該鋳型内溶鋼にBiおよびSnの内から1種以上を合計で溶鋼中含有量が0.0005〜0.01質量%になるように添加せしめ、該誘導電磁攪拌装置により水平面内で溶鋼を旋回させながら鋳造することを特徴とする連続鋳造方法。 C: 0.03 to 0.20% by mass, Si: 0.08 to 1.5% by mass, Mn: 0 using a continuous casting apparatus having an induction electromagnetic stirrer between the in-mold meniscus and the under-mold 10 m. .5 to 3.0 mass%, P: 0.05 mass% or less, S: 0.002 mass% or more, N: 0.0005 to 0.01 mass%, Nb: 0.2 mass% or less, V: 0.2% by mass or less, Mo: 0.5% by mass or less, acid-soluble Al: 0.03% by mass or less, acid-soluble Ti: less than 0.1% by mass, among Ce, La, Nd or Pr, A molten steel containing at least one of a total of 0.0003 to 0.02 mass% and the balance consisting of iron and unavoidable impurities is injected into the mold, and the molten steel in the mold is one of Bi and Sn. allowed added to the molten steel content is 0.0005 to 0.01 mass% in total of the above, the induction Continuous casting wherein the casting while swirling the molten steel in a horizontal plane by 磁攪 拌 device. BiおよびSnの内から1種以上を含有する金属ワイヤーを鋳型内溶鋼中に連続的に供給することを特徴とする請求項1記載の連続鋳造方法。   The continuous casting method according to claim 1, characterized in that a metal wire containing one or more of Bi and Sn is continuously fed into molten steel in a mold. BiおよびSnの内から1種以上を含有するモールドフラックスを鋳型内溶鋼表面上に供給することを特徴とする請求項1記載の連続鋳造方法。   The continuous casting method according to claim 1, wherein a mold flux containing one or more of Bi and Sn is supplied onto the molten steel surface in the mold. 誘導電磁攪拌による溶鋼の旋回流速を、鋳片の幅方向中央部の固液界面において25〜105cm/sとすることを特徴とする請求項1〜3のいずれか1項記載の連続鋳造方法。 The continuous casting method according to any one of claims 1 to 3, wherein the swirling flow velocity of the molten steel by induction electromagnetic stirring is set to 25 to 105 cm / s at the solid-liquid interface in the widthwise central portion of the slab . 請求項4記載の連続鋳造方法により鋳片の表層から1/4厚、1/4厚から内部のそれぞれについて平均等軸晶粒径を3mm以下にしたことを特徴とする連続鋳造鋳片。   A continuous cast slab characterized in that the average equiaxed grain size is 3 mm or less for each of 1⁄4 thickness and 1/4 thickness from the surface layer of the slab by the continuous casting method according to claim 4.
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