JP5167628B2 - Steel slab with fine solidification structure - Google Patents
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Description
本発明は、凝固組織が微細な鋼鋳片に関するものであり、特に、鋼がδ凝固する際に、等軸晶の生成を促すことで凝固組織を有利に微細化することのできる酸化物を含有する、凝固組織が微細な鋼鋳片に関する。本発明の凝固組織が微細な鋼鋳片は、主として鉄鋼業の製鋼工程に適用されるものであり、本発明を適用した鋼鋳片は、鋼板、鋼管、形鋼、棒鋼、線材など各種の鉄鋼製品の素材として使用される。 The present invention relates to a steel slab having a fine solidification structure, and in particular, an oxide that can advantageously refine the solidification structure by promoting the formation of equiaxed crystals when the steel solidifies δ. It relates to a steel slab containing a fine solidified structure. The steel slab with a fine solidification structure of the present invention is mainly applied to the steelmaking process of the steel industry, and the steel slab to which the present invention is applied includes various steel plates, steel pipes, shaped steel, bar steel, wire rods and the like. Used as a material for steel products.
鋼板、鋼管、形鋼、棒鋼、鋼線材等の鉄鋼製品は、引張特性や破壊特性等の様々な機械的性質が要求され、ユーザーからの要求レベルは年々高まっている。さらに、鉄鋼製品市場のグローバル化に伴う競争の熾烈化により、機械的性質等の品質のみならず、納期短縮や低価格化等についても、競争力の重要な指標として位置づけられるようになっている。 Steel products such as steel plates, steel pipes, shaped steels, steel bars, and steel wires are required to have various mechanical properties such as tensile properties and fracture properties, and the level of demand from users is increasing year by year. Furthermore, due to intensifying competition accompanying the globalization of the steel products market, not only quality such as mechanical properties but also shortening of delivery time and lowering prices are becoming important indicators of competitiveness. .
鉄鋼製品の品質、納期、価格を左右する機械的性質、製造時間、製造コストは、素材であるスラブ、ブルーム、ビレット等の鋼鋳片の品質に大きく影響される。鋼鋳片には、凝固偏析やポロシティ等の組成不均質部や空隙が存在する。これらの鋳造欠陥が鉄鋼製品の品質に与える悪影響を軽減するために、連続鋳造における低温鋳造処理や電磁攪拌処理、軽圧下処理、熱間加工に先立つ鋼鋳片の均質化熱処理、熱間加工における高温強加工処理等の多大な製造負荷が発生し、製造時間が長くなり、製造コストが上昇するという問題がある。さらには、鉄鋼製品の高機能化要求に対して、素材の鋳造欠陥が障害となって機械的性質の向上が阻まれる場合も多く、上記問題を解決するため、鋳造欠陥を抜本的に改善する技術が望まれている。 The mechanical properties, production time, and production cost that affect the quality, delivery date, and price of steel products are greatly affected by the quality of steel slabs such as slabs, blooms, and billets. In steel slabs, there are compositionally inhomogeneous parts and voids such as solidification segregation and porosity. In order to reduce the negative effects of these casting defects on the quality of steel products, low-temperature casting processing, electromagnetic stirring processing, light reduction processing in continuous casting, homogenization heat treatment of steel slabs prior to hot working, and hot working There is a problem that a large manufacturing load such as high-temperature high-strength processing occurs, the manufacturing time becomes long, and the manufacturing cost increases. Furthermore, in response to demands for higher functionality of steel products, there are many cases where the casting defects of the material hinder the improvement of the mechanical properties, and in order to solve the above problems, the casting defects are drastically improved. Technology is desired.
鋼鋳片の凝固偏析やポロシティを微細化して従来よりも無害化できれば、上述した製造負荷が軽減され、また、高機能化に対する障害も取り除かれるため、鉄鋼製品の品質、納期、価格の競争力が向上する可能性がある。凝固偏析やポロシティを微細化して無害化する手段として、接種技術によって凝固等軸晶の生成を促し、その粒径を微細化する方法があり、このような方法の有効性が以下に説明する特許文献によって知られている。 If the solidification segregation and porosity of steel slabs can be refined and made harmless than before, the manufacturing load mentioned above will be reduced, and the obstacles to high functionality will be removed, so the quality, delivery date, and price competitiveness of steel products May improve. As a means of detoxifying solidification segregation and porosity, there is a method of promoting the generation of solidified equiaxed crystals by inoculation technology and making the particle size finer, and patents that explain the effectiveness of such methods are described below Known by the literature.
低炭素鋼やフェライト系ステンレス鋼のように、凝固初相がδ−Feである場合の接種核として、特許文献1に記載の発明ではREM系の酸化物や硫化物や酸硫化物の有効性が、特許文献2に記載の発明ではBa系酸化物の有効性が、特許文献3に記載の発明では単独TiNあるいはMg系酸化物に複合するTiNの有効性が、特許文献4〜6に記載の発明ではMg系酸化物の有効性が、それぞれ開示されている。
一方、高炭素鋼やオーステナイト系ステンレス鋼のように、凝固初相がγ−Feである場合の接種核として、ZrO2、MgS、CaO、REM系窒化物、Ti2O3などの有効性が知見されている。
As an inoculation nucleus when the solidification initial phase is δ-Fe, such as low carbon steel and ferritic stainless steel, in the invention described in Patent Document 1, the effectiveness of REM oxides, sulfides and oxysulfides However, in the invention described in Patent Document 2, the effectiveness of Ba-based oxides is described, and in the invention described in Patent Document 3, effectiveness of TiN compounded with a single TiN or Mg-based oxide is described in Patent Documents 4-6. In this invention, the effectiveness of Mg-based oxides is disclosed.
On the other hand, ZrO 2 , MgS, CaO, REM nitride, Ti 2 O 3, etc. are effective as inoculation nuclei when the solidification initial phase is γ-Fe, such as high carbon steel and austenitic stainless steel. It has been found.
上述のように、凝固初相の結晶構造がδ−Feとγ−Feの場合とでは、有効な接種核の種類が異なる。これは、非特許文献1に記載されているように、凝固初相との格子不整合度が小さい物質ほど凝固核としての能力が高く、凝固等軸晶の生成を促進すると考えられることから、凝固初相の結晶構造に応じて接種核の有効性が異なるためと判断することができる。
しかしながら、凝固初相がδ−Feである鋼において、溶鋼の脱酸反応、脱硫反応、脱窒反応を利用して上述した既知の接種核を生成させる場合、以下のような問題があり、工業的な適用に限界があることが明らかとなった。即ち、上記特許文献1に記載の発明のように、溶鋼中でREM系の酸化物や硫化物、さらにはこれらの複合析出物を生成させるためにREMを添加すると、粗大なREM介在物が生成し、連続鋳造ノズルの閉塞や鉄鋼製品の品質劣化を引き起こす虞がある。 However, in the steel whose solidification initial phase is δ-Fe, when the above-mentioned known inoculation nuclei are generated using the deoxidation reaction, desulfurization reaction, and denitrification reaction of molten steel, there are the following problems, It became clear that there was a limit to the practical application. That is, as in the invention described in Patent Document 1, when REM is added in order to produce REM oxides and sulfides, and further composite precipitates thereof in molten steel, coarse REM inclusions are produced. In addition, the continuous casting nozzle may be blocked and the quality of steel products may be deteriorated.
また、上記特許文献2に記載の発明のように、溶鋼中でBa系酸化物を生成させるためにBaを添加する場合や、上記特許文献3〜6に記載の発明のように、溶鋼中でMg系酸化物を生成させるためにMgを添加する場合には、これらの元素は蒸発ロスが大きく歩留まりが低いため、添加方法の制約や合金コストの上昇、さらには鋼中含有量が不安定になるという問題が生じる虞がある。 Moreover, when adding Ba in order to produce | generate Ba type | system | group oxide in molten steel like the invention of the said patent document 2, or in the molten steel like the invention of the said patent documents 3-6, When adding Mg to produce Mg-based oxides, these elements have large evaporation losses and low yields, so restrictions on the addition method, increase in alloy costs, and unstable steel content There is a possibility that the problem of becoming.
また、上記特許文献3に記載の発明のような、溶鋼中でTiNを生成させるために多量のNを添加する方法を低Cr鋼に用いることは困難であり、また、多量のTiを添加する方法を用いた場合には、溶接構造用鋼の母材や溶接熱影響部(HAZ)を過度に硬化させて機械的性質を損なう虞がある。
上述のような問題から、凝固初相がδ−Feである鋼鋳片の製造において、有害な粗大介在物が生成せず、溶鋼への元素添加が容易で、多量のTiやNを必要としない、新しい接種技術が求められていた。
Moreover, it is difficult to use a method for adding a large amount of N to low Cr steel in order to generate TiN in molten steel, such as the invention described in Patent Document 3, and a large amount of Ti is added. When the method is used, the base material of the welded structural steel or the weld heat affected zone (HAZ) may be excessively cured to impair mechanical properties.
Due to the problems described above, in the production of steel slabs whose solidification initial phase is δ-Fe, no harmful coarse inclusions are generated, element addition to molten steel is easy, and a large amount of Ti or N is required. No new inoculation technology was required.
本発明は上記問題に鑑みてなされたものであり、凝固初相がδ−Feである鋼鋳片の偏析やポロシティを微細化して有利に無害化することのできる、凝固組織が微細な鋼鋳片を提供することを目的とする。 The present invention has been made in view of the above-mentioned problems, and it is possible to make the segregation and porosity of steel slabs whose solidification initial phase is δ-Fe finer, and to make them harmless, and to make them harmless. The purpose is to provide a piece.
本発明者らは、鋼鋳片の含有成分に関して鋭意検討した結果、溶鋼の脱酸反応で生ずる酸化物を凝固核として利用して凝固等軸晶の生成を促し、その粒径を微細化することにより、凝固初相がδ−Feである鋼鋳片の偏析やポロシティを微細化して有利に無害化することができ、凝固組織が微細な鋼鋳片が得られることを知見した。
本発明は上述の知見に基づいて構成されており、その主旨とするところは以下の通りである。
As a result of intensive studies on the components contained in the steel slab, the present inventors have promoted the formation of solidified equiaxed crystals by using the oxide produced by the deoxidation reaction of molten steel as the solidification nuclei, and refined the particle size. As a result, it was found that the segregation and porosity of the steel slab whose solidification initial phase is δ-Fe can be refined and made harmless advantageously, and a steel slab having a fine solidification structure can be obtained.
The present invention is configured based on the above-described knowledge, and the main points thereof are as follows.
(1) 鋼鋳片の成分組成が、質量%で、C:0.5%以下、S:0.01%以下、N:0.05%以下、O:0.001〜0.01%、Al:0.001〜0.1%、Ca:0.0020〜0.005%を含有し、さらに、Zr:0.0005〜0.05%、Hf:0.001〜0.1%の内の1種又は2種を含有し、残部が鉄及び不可避的不純物からなり、凝固初相がδ−Feとなる鋼鋳片であって、該鋼鋳片中の酸化物の内、Caと、Zr及びHfの内の1種又は2種とを同時に含み、その表面の全部又は一部が第三物質を介することなく地鉄に直接接触するように存在するとともに、0.1〜10μmの最大径を有するCaX系酸化物が、単独粒子あるいは複合粒子として、任意断面において面積1mm2当たりで1個以上存在することを特徴とする、凝固組織が微細な鋼鋳片。但し、前記CaX系酸化物のXは、Zr及びHfの内の1種又は2種である。
(1) The composition of the steel slab is mass%, C: 0.5% or less, S: 0.01% or less, N: 0.05% or less, O: 0.001 to 0.01%, Al: 0.001 to 0.1%, Ca: 0.0020 to 0.005%, Zr: 0.0005 to 0.05%, Hf: 0.001 to 0.1% Is a steel slab containing iron and unavoidable impurities, and the solidification initial phase is δ-Fe, and among the oxides in the steel slab, Ca, One or two of Zr and Hf are included at the same time, and all or a part of the surface thereof is present in direct contact with the ground iron without passing through a third substance, and a maximum of 0.1 to 10 μm CaX-based oxide having a diameter of, alone particles or composite particles, there are one or more in an area 1 mm 2 per in any cross-section It characterized the door, equiaxed grain structures steel slab. However, X of the CaX-based oxide is one or two of Zr and Hf.
(2) 溶鋼中における脱酸力がAlよりも小さな成分である、Si、Mn、Nb、V、Cu、Ni、Cr、Mo、Bの内の1種又は2種以上を含有するとともに、これらの成分の含有量が、下記(1)式で計算されるCr当量が30質量%以下となり、且つ、下記(2)式で計算されるNi当量が15質量%以下となる含有量とされていることを特徴とする、請求項1に記載の凝固組織が微細な鋼鋳片。
Cr当量=Cr+Mo+1.5Si+0.5Nb+21.4Al+40B+8.29V ・・・(1)
Ni当量=Ni+30C+30N+0.5Mn+0.16Cu ・・・(2)
(2) While containing 1 type or 2 or more types in Si, Mn , Nb, V, Cu, Ni, Cr, Mo , B which is a component whose deoxidizing power in molten steel is smaller than Al, The content of these components is such that the Cr equivalent calculated by the following formula (1) is 30% by mass or less and the Ni equivalent calculated by the following formula (2) is 15% by mass or less. The steel slab having a fine solidification structure according to claim 1, wherein
Cr equivalent = Cr + Mo + 1.5Si + 0.5Nb + 21.4Al + 40B + 8.29V (1)
Ni equivalent = Ni + 30C + 30N + 0.5Mn + 0.16Cu (2)
本発明の凝固組織が微細な鋼鋳片によれば、凝固組織の微細化を通じて偏析やポロシティが微細化され、従来よりも無害化される効果を有しており、延いては、鋳造欠陥の悪影響を軽減する目的で行われる負荷工程を軽減することができ、また、高機能化要求に対する鋳片起因の障害を取り除くことができる。このような、本発明の凝固組織が微細な鋼鋳片を用いることにより、品質、納期、価格面等における競争力の高い鉄鋼製品を有利に提供することができることから、その産業上の効果は計り知れない。 According to the steel slab with a fine solidification structure of the present invention, segregation and porosity are refined through refinement of the solidification structure, and the effect of making it harmless than before, and eventually, the casting defect It is possible to reduce the load process performed for the purpose of reducing the adverse effect, and it is possible to remove the obstacle caused by the slab with respect to the demand for higher functionality. By using a steel slab having a fine solidification structure of the present invention, it is possible to advantageously provide steel products with high competitiveness in terms of quality, delivery time, price, etc. unfathomable.
以下、本発明の凝固組織が微細な鋼鋳片の実施の形態について説明する。
なお、この実施形態は、発明の趣旨をより良く理解させるために詳細に説明するものであるから、特に指定の無い限り、本発明を限定するものではない。
Hereinafter, embodiments of a steel slab having a fine solidified structure according to the present invention will be described.
In addition, since this embodiment is described in detail for better understanding of the gist of the invention, the present invention is not limited unless otherwise specified.
本発明の凝固組織が微細な鋼鋳片(以下、鋼鋳片と略称することがある)は、Cの含有量が0.5質量%以下であり、凝固初相がδ−Feとなる鋼鋳片であって、該鋼鋳片中の酸化物の内、Caを必須とし、さらに、Zr及びHfの内の1種又は2種を主成分とし、その表面の全部又は一部が第三物質を介することなく地鉄に直接接触するように存在するとともに、0.1〜10μmの最大径を有する酸化物が、単独粒子あるいは複合粒子として、任意断面において面積1mm2当たりで1個以上存在し、概略構成されている。 The steel slab having a fine solidification structure of the present invention (hereinafter sometimes abbreviated as steel slab) is a steel having a C content of 0.5 mass% or less and a solidification initial phase of δ-Fe. It is a slab, Ca is essential among the oxides in the steel slab, and one or two of Zr and Hf are the main components, and all or part of the surface is third. One or more oxides having a maximum diameter of 0.1 to 10 μm exist as single particles or composite particles per area of 1 mm 2 in an arbitrary cross-section as they are in direct contact with the base iron without any substance. And it is schematically configured.
また、本実施形態の凝固組織が微細な鋼鋳片は、鋼鋳片の成分組成が、質量%で、C:0.5%以下、S:0.01%以下、N:0.05%以下、O:0.001〜0.01%、Al:0.001〜0.1%、Ca:0.0005〜0.005%を含有し、さらに、Zr:0.0005〜0.05%、Hf:0.001〜0.1%の内の1種又は2種を含有し、残部が鉄及び不可避的不純物とされている。 Further, in the steel slab having a fine solidification structure according to this embodiment, the component composition of the steel slab is mass%, C: 0.5% or less, S: 0.01% or less, N: 0.05%. Hereinafter, O: 0.001 to 0.01%, Al: 0.001 to 0.1%, Ca: 0.0005 to 0.005%, Zr: 0.0005 to 0.05% , Hf: One or two of 0.001 to 0.1% are contained, the balance being iron and inevitable impurities.
本発明者らは、凝固初相がδ−Feである鋳片の製造において、有害な粗大介在物が生成せず、溶鋼への元素添加が容易で、多量のTiやNを必要としない、新しい接種技術について鋭意検討した。その結果、従来知られていない新しい種類の接種核を見出し、本発明を完成するに至った。この新しい接種核は、CaとX(X:ZrおよびHfのうちの1種または2種。以下、単にXと略称することがある。)を主成分とする酸化物(以下、CaX系酸化物と略称することがある。)であった。
即ち、酸化物が溶鋼の脱酸反応によって生成する場合に、鋳片のδ凝固組織において等軸晶の面積率が増えて柱状晶の面積率が減少し、同時に、等軸晶の粒径が微細化するような接種効果が認められた鋳片、あるいは、これを加工した製品の任意断面において酸化物を解析した結果、波長分散型X線分析法(WDS)で測定された酸化物組成は、CaとXを同時に含有しているという特徴が確認された。また、電子線回折で同定された酸化物の結晶構造は、個々の酸化物粒子の全体あるいは一部がペロブスカイト構造(CaTiO3構造)を有するという特徴が確認された。さらに、酸化物を構成するXが主にZrの場合には、斜方ペロブスカイト構造(格子定数:a=0.576nm、b=0.802nm、c=0.559nm)を有するCaZrO3と同定される酸化物が多く確認された。
In the production of a slab in which the solidification initial phase is δ-Fe, the present inventors do not generate harmful coarse inclusions, it is easy to add elements to the molten steel, and a large amount of Ti or N is not required. The new inoculation technique was studied earnestly. As a result, a new type of inoculum nucleus not known in the past has been found and the present invention has been completed. This new inoculum nucleus is an oxide (hereinafter referred to as CaX-based oxide) mainly composed of Ca and X (X: one or two of Zr and Hf, hereinafter may be simply referred to as X). May be abbreviated as ")".
That is, when the oxide is produced by the deoxidation reaction of the molten steel, the area ratio of equiaxed crystals increases in the δ solidified structure of the slab, and the area ratio of columnar crystals decreases. As a result of analyzing oxides in the slab where the inoculation effect such as miniaturization was recognized, or in the arbitrary cross section of the processed product, the oxide composition measured by wavelength dispersive X-ray analysis (WDS) is The characteristics of containing Ca and X at the same time were confirmed. Further, the crystal structure of the oxide identified by electron beam diffraction was confirmed to have a characteristic that all or part of each oxide particle has a perovskite structure (CaTiO 3 structure). Further, when X constituting the oxide is mainly Zr, it is identified as CaZrO 3 having an orthorhombic perovskite structure (lattice constants: a = 0.576 nm, b = 0.802 nm, c = 0.559 nm). Many oxides were confirmed.
ここで、CaZrO3の(010)面にδ−Feの{100}面が核生成する場合を仮定すると、前記非特許文献1において定義される格子不整合度は3.1%と見積もることができる。従来より、δ−Fe接種能が高いことで知られるTiNの格子不整合度は3.9%、Ce2O3のそれは5.0%であるので、当該酸化物CaZrO3は、これら既知の接種核よりもδ−Feに対する格子不整合度が小さく、接種能が高いものと考えられる。当該酸化物CaZrO3の表面には、X系窒化物やCa系硫化物が部分的に複合析出している場合(本発明では、CaX系酸化物の単独粒子に対して、このような場合の析出物の粒子を複合粒子ともいう)があったが、酸化物CaZrO3の表面がこれらの窒化物や硫化物で全て覆われることはなく、酸化物表面の全部あるいは一部がX系窒化物やCa系硫化物等の第三物質を介することなく地鉄に直接接する形態で観察された。 Here, assuming that the {100} plane of δ-Fe nucleates on the (010) plane of CaZrO 3, the lattice mismatch degree defined in Non-Patent Document 1 can be estimated to be 3.1%. it can. Conventionally, the lattice mismatch degree of TiN, which is known to have a high δ-Fe inoculation ability, is 3.9%, and that of Ce 2 O 3 is 5.0%. Therefore, the oxide CaZrO 3 is known in the art. It is considered that the degree of lattice mismatch with respect to δ-Fe is smaller than that of inoculated nuclei and the inoculation ability is high. In the case where X-based nitride or Ca-based sulfide is partially complex-precipitated on the surface of the oxide CaZrO 3 (in the present invention, in the case of such a case with respect to a single particle of CaX-based oxide) However, the surface of the oxide CaZrO 3 is not entirely covered with these nitrides or sulfides, and all or part of the oxide surface is X-based nitride. It was observed in a form that was in direct contact with the steel without passing through a third substance such as Ca or Ca-based sulfide.
一方、SやNを多量に添加し、さらに、CaやXを多量に添加した鋼では、接種効果は小さかった。このような接種効果が小さい鋳片には、上述した同様のCaX系酸化物が存在するものの、CaX系酸化物の表面がX系窒化物やCa系硫化物でほぼ全て覆われており、CaX系酸化物表面が地鉄に直接接する部分は皆無であった。CaX系酸化物表面を全て覆い隠す粗大な窒化物や硫化物は主に溶鋼中で生成しており、このような場合のCaX系酸化物は溶鋼に直接接触していないため、格子不整合度の観点から期待される接種効果が発揮できていないものと推察される。
以上により、本発明者等によって新たに見出された接種核の組成と形態の特徴は、CaとXを主成分とする酸化物であり、地鉄(溶鋼)に対して酸化物表面の全部あるいは一部が第三物質を介することなく直接接触していることである。
On the other hand, the inoculation effect was small in the steel added with a large amount of S and N and further added with a large amount of Ca and X. Such a slab with a small inoculation effect has the same CaX-based oxide as described above, but the surface of the CaX-based oxide is almost entirely covered with X-based nitride and Ca-based sulfide. There was no portion where the surface of the system oxide was in direct contact with the steel. Coarse nitrides and sulfides that cover the entire surface of the CaX-based oxide are mainly generated in the molten steel. In such cases, the CaX-based oxide is not in direct contact with the molten steel. It is presumed that the inoculation effect expected from this point of view is not achieved.
From the above, the characteristics of the composition and form of the inoculum nucleus newly found by the present inventors are oxides mainly composed of Ca and X, and the entire surface of the oxide with respect to the base iron (molten steel). Alternatively, a part is in direct contact without a third substance.
接種核としての能力が高く、また、その個数が多いほど、凝固組織における接種効果は高まることになるが、その接種核の能力は、上述した接種核の組成や形態の他、その寸法が影響する。さらには、接種核の寸法が大きいほど接種核の能力は高まるが、その反面、接種核の個数が減少してしまうという不利益が考えられる。従って、接種効果を安定的に発現するためには、接種核の組成と形態に加えて、その寸法と個数を適正に制御することが重要である。
本発明で新たに見出されたCaX系酸化物の接種核について、適正な粒子径と個数を検討した結果、酸化物の最大径が0.1〜10μmであり、任意断面の面積1mm2当たりで1個以上存在させた場合に、接種効果が安定的に発現することが明らかとなった。酸化物の最大径が0.1μm未満の場合には接種能力が低く、また、酸化物の最大径が10μmを超える場合には個数が1mm2当たり1個未満となって接種能力が低下するため、上記粒子径及び個数が必要である。
The higher the number of inoculum nuclei and the greater the number, the greater the inoculation effect on the coagulated tissue. However, in addition to the composition and form of the inoculum nuclei described above, the size of the inoculum nuclei has an effect. To do. Furthermore, the larger the size of the seeded nucleus, the higher the capacity of the seeded nucleus. On the other hand, there is a disadvantage that the number of seeded cores decreases. Therefore, in order to stably develop the inoculation effect, it is important to appropriately control the size and number in addition to the composition and form of the inoculum nucleus.
As a result of examining the appropriate particle diameter and number of CaO-based oxide inoculation nuclei newly found in the present invention, the maximum diameter of the oxide is 0.1 to 10 μm, and the area of an arbitrary cross section is 1 mm 2 . It was revealed that the inoculation effect was stably expressed when one or more were present. When the maximum diameter of oxide is less than 0.1 μm, the inoculation capacity is low, and when the maximum diameter of oxide exceeds 10 μm, the number is less than 1 per 1 mm 2 and the inoculation capacity decreases. The above particle diameter and number are necessary.
<鋼鋳片の化学成分組成>
上述のような組成、形態、寸法および個数を有するCaX系酸化物を鋼中に生成させるためには、凝固初相がδ−Feとなる鋼の化学成分を適正に調整するのが好ましい。
以下に、本発明で規定する化学成分組成の限定理由を説明する。
<Chemical composition of steel slab>
In order to produce CaX-based oxides having the composition, form, dimensions, and number as described above in the steel, it is preferable to appropriately adjust the chemical components of the steel in which the solidification initial phase is δ-Fe.
Below, the reason for limitation of the chemical component composition prescribed | regulated by this invention is demonstrated.
[C(炭素):0.5%以下]
Cの含有量は、0.5%以下とする必要がある。Cが0.5%を超えると、凝固初相がδ−Feからγ−Feに変化するため、CaX系酸化物の格子不整合度に期待する接種効果が得られない。
[C (carbon): 0.5% or less]
The C content needs to be 0.5% or less. When C exceeds 0.5%, the solidification initial phase changes from δ-Fe to γ-Fe, so that the inoculation effect expected for the degree of lattice mismatch of the CaX-based oxide cannot be obtained.
[S(硫黄):0.01%以下]
Sの含有量は、0.01%以下とするのが好ましい。Sが0.01%を超えると、溶鋼中で粗大なCaSが生成し、脱酸のためのCaが不足してCaX酸化物を安定的に生成させることができなくなる虞がある。また、Caが多い場合にSを過剰添加すると、溶鋼中に生成した粗大なCaSがCaX系酸化物の表面を覆い隠し、接種核の能力を低下させる虞があるからである。
[S (sulfur): 0.01% or less]
The S content is preferably 0.01% or less. If S exceeds 0.01%, coarse CaS is produced in the molten steel, and there is a possibility that Ca for deoxidation is insufficient and CaX oxide cannot be produced stably. Moreover, when S is added excessively when there is a large amount of Ca, coarse CaS generated in the molten steel may cover the surface of the CaX-based oxide and reduce the ability of the seeding nucleus.
[N(窒素):0.05%以下]
Nの含有量は、0.05%以下とするのが好ましい。Nが0.05%を超えると、溶鋼中で粗大なXNが生成し、脱酸のためのXが不足してCaX酸化物を安定的に生成させることができなくなる虞がある。また、Xが多い場合にNを過剰添加すると、溶鋼中に生成した粗大なXNがCaX系酸化物の表面を覆い隠し、接種核の能力を低下させる虞があるからである。
[N (nitrogen): 0.05% or less]
The N content is preferably 0.05% or less. If N exceeds 0.05%, coarse XN is generated in the molten steel, and there is a possibility that X for deoxidation is insufficient and CaX oxide cannot be stably generated. In addition, if N is excessively added when X is large, coarse XN generated in the molten steel may cover the surface of the CaX-based oxide and reduce the ability of the seeding nucleus.
[O(酸素):0.001〜0.01%]
Oの含有量は、0.001〜0.01%にするのが好ましい。Oが0.001%未満では、CaX系酸化物の粒子径と個数が不足する虞がある。また、Oが0.01%を超えると、CaX系酸化物の粒子径が粗大化し、その個数が不足すると同時に、鉄鋼製品の品質に有害性をもたらす虞があるからである。
[O (oxygen): 0.001 to 0.01%]
The O content is preferably 0.001 to 0.01%. If O is less than 0.001%, the particle diameter and number of CaX-based oxides may be insufficient. Further, if O exceeds 0.01%, the particle diameter of the CaX-based oxide becomes coarse, and the number thereof is insufficient, and at the same time, there is a possibility that the quality of the steel product may be harmful.
[Al(アルミニウム):0.001〜0.1%]
Alの含有量は、0.001〜0.1%とするのが好ましい。Alが0.001%未満では、O量を安定的に0.01%以下に低減することができなくなる虞がある。また、Alが0.1%を超えると、酸化物中のAl含有量が増加してCaX系酸化物を安定的に生成させることができなくなる虞がある。さらに、Oが多い場合にAlを過剰添加すると、粗大なアルミナクラスターが生成し、鋳造ノズルが閉塞したり、鉄鋼製品の品質が劣化する虞があるからである。
[Al (aluminum): 0.001 to 0.1%]
The Al content is preferably 0.001 to 0.1%. If Al is less than 0.001%, the amount of O may not be stably reduced to 0.01% or less. On the other hand, if Al exceeds 0.1%, the Al content in the oxide may increase and the CaX-based oxide may not be stably generated. Furthermore, when Al is excessively added when O is large, coarse alumina clusters are generated, and there is a possibility that the casting nozzle is blocked and the quality of the steel product is deteriorated.
[Ca(カルシウム):0.0005〜0.005%]
Caの含有量は、0.0005〜0.005%とするのが好ましい。Caが0.0005%未満では、酸化物中のCa含有量が減少してCaX系酸化物を安定的に生成させることができなくなる虞がある。また、Caが0.005%を超えると、酸化物中のCa含有量が増加してCaX系酸化物を安定的に生成させることができなくなる虞がある。さらに、Sが多い場合にCaを過剰添加すると、溶鋼中で粗大なCaSが生成してCaX系酸化物の表面を覆い隠し、接種核の能力を低下させる虞があるからである。
[Ca (calcium): 0.0005 to 0.005%]
The Ca content is preferably 0.0005 to 0.005%. If Ca is less than 0.0005%, the Ca content in the oxide may be reduced, and the CaX-based oxide may not be stably generated. On the other hand, if Ca exceeds 0.005%, the Ca content in the oxide may increase, and it may not be possible to stably generate the CaX-based oxide. Further, when Ca is excessively added when there is a large amount of S, coarse CaS is generated in the molten steel, covering the surface of the CaX-based oxide, which may reduce the ability of the seeding nucleus.
[Zr(ジルコニウム):0.0005〜0.05%]
Zrの含有量は、0.0005〜0.05%とするのが好ましい。Zrが0.0005%未満では、酸化物中のZr含有量が減少してCaX系酸化物を安定的に生成させることができなくなる虞がある。また、Zrが0.05%を超えると、酸化物中のZr含有量が増加してCaX系酸化物を安定的に生成させることができなくなる虞がある。さらに、Nが多い場合にZrを過剰添加すると、溶鋼中で粗大なZrNが生成してCaX系酸化物の表面を覆い隠し、接種核の能力を低下させる虞がある。また、さらに、過剰なZr添加は合金コストの上昇を招くため好ましくないからである。
[Zr (zirconium): 0.0005 to 0.05%]
The Zr content is preferably 0.0005 to 0.05%. If Zr is less than 0.0005%, the Zr content in the oxide may be reduced, and the CaX-based oxide may not be stably generated. On the other hand, if Zr exceeds 0.05%, the Zr content in the oxide may increase, and the CaX-based oxide may not be stably generated. Furthermore, when Zr is excessively added when N is large, coarse ZrN is generated in the molten steel, covering the surface of the CaX-based oxide, which may reduce the ability of the seeding nucleus. Furthermore, excessive Zr addition is not preferable because it increases the alloy cost.
[Hf(ハフニウム):0.001〜0.1%]
Hfの含有量は、0.001〜0.1%とするのが好ましい。Hfが0.001%未満では、酸化物中のHf含有量が減少してCaX系酸化物を安定的に生成させることができなくなる虞がある。また、Hfが0.1%を超えると、酸化物中のHf含有量が増加してCaX系酸化物を安定的に生成させることができなくなる虞がある。さらに、Nが多い場合にHfを過剰添加すると、溶鋼中で粗大なHfNが生成してCaX系酸化物の表面を覆い隠し、接種核の能力を低下させる虞がある。また、さらに、過剰なHf添加は合金コストの上昇を招くため好ましくないからである。
[Hf (hafnium): 0.001 to 0.1%]
The Hf content is preferably 0.001 to 0.1%. If Hf is less than 0.001%, the Hf content in the oxide may decrease, and the CaX-based oxide may not be stably generated. On the other hand, if Hf exceeds 0.1%, the Hf content in the oxide may increase, and the CaX-based oxide may not be stably generated. Further, when Hf is excessively added when N is large, coarse HfN is generated in the molten steel, covering the surface of the CaX-based oxide, which may reduce the ability of the seeding nucleus. Furthermore, excessive Hf addition is undesirable because it increases the alloy cost.
[その他の化学成分]
本発明の凝固組織が微細な鋼鋳片では、さらに必要に応じて、溶鋼中における脱酸力がAlよりも小さい他の元素を添加してもよい。
即ち、Alよりも脱酸力の強いREMやBa、Mgなどを添加すると、脱酸反応においてCaやXと競合するため、本発明のCaX系酸化物を安定的に生成させることができない。
一方、Alよりも脱酸力の小さな成分であるSi、Mn、Cu、Ni、Cr、Mo、Nb、V、Bの内の1種又は2種以上の元素を、凝固初相がδ−Feとなる範囲内で添加した場合にも本発明の効果が得られる。但し、この際、下記(1)式で計算されるCr当量は30%以下とする必要がある。Cr当量が30%を超えると、耐食性や耐熱性などの冶金効果は飽和し、合金コストの上昇を招くため好ましくないからである。
さらに、本発明の鋼鋳片では、下記(2)式で計算されるNi当量を15%以下とする必要がある。Ni当量が15%を超えると、凝固初相がδ−Feからγ−Feに変化するため、CaX系酸化物の格子不整合度に期待した接種効果が得られないからである。
Cr当量=Cr+Mo+1.5Si+0.5Nb+21.4Al+40B
+8.29V ・・・(1)
Ni当量=Ni+30C+30N+0.5Mn+0.16Cu ・・・(2)
[Other chemical components]
In the steel slab having a fine solidification structure according to the present invention, another element having a deoxidizing power in molten steel smaller than that of Al may be added as necessary.
That is, when REM, Ba, Mg, or the like having a stronger deoxidizing power than Al is added, the CaX-based oxide of the present invention cannot be stably generated because it competes with Ca and X in the deoxidation reaction.
On the other hand, one or more elements of Si, Mn, Cu , Ni, Cr, Mo , Nb, V, and B, which are components having a deoxidizing power smaller than that of Al, have a solidification initial phase of δ The effect of the present invention can also be obtained when it is added within the range of -Fe. However, in this case, the Cr equivalent calculated by the following equation (1) needs to be 30% or less. This is because if the Cr equivalent exceeds 30%, the metallurgical effects such as corrosion resistance and heat resistance are saturated and the alloy cost is increased, which is not preferable.
Furthermore, in the steel slab of the present invention, the Ni equivalent calculated by the following equation (2) needs to be 15% or less. This is because if the Ni equivalent exceeds 15%, the solidification initial phase changes from δ-Fe to γ-Fe, so that the inoculation effect expected for the degree of lattice mismatch of the CaX-based oxide cannot be obtained .
C r eq = Cr + Mo + 1.5Si + 0.5Nb + 21.4Al + 40B
+ 8.29V (1)
Ni equivalent = Ni + 30C + 30N + 0.5Mn + 0.16Cu (2)
以上説明したように、本発明の凝固組織が微細な鋼鋳片は、上記構成により、凝固組織の微細化を通じて偏析やポロシティが微細化され、従来よりも無害化される効果を有しており、延いては、鋳造欠陥の悪影響を軽減する目的で行われる負荷工程を軽減することができ、また、高機能化要求に対する鋳片起因の障害を取り除くことができる。また、本発明の凝固組織が微細な鋼鋳片を用いることにより、品質、納期、価格面等における競争力の高い鉄鋼製品を有利に提供することができることから、その産業上の効果は計り知れない。 As described above, the steel slab having a fine solidification structure according to the present invention has the effect of making the segregation and porosity finer through the refinement of the solidification structure and making it harmless than the conventional structure. As a result, it is possible to reduce the loading process performed for the purpose of reducing the adverse effects of casting defects, and it is possible to remove the obstacle caused by the slab for the demand for higher functionality. In addition, by using a steel slab having a fine solidification structure according to the present invention, it is possible to advantageously provide steel products having high competitiveness in terms of quality, delivery time, price, etc., and its industrial effects are immeasurable. Absent.
以下、本発明に係る凝固組織が微細な鋼鋳片の実施例を挙げ、本発明をより具体的に説明するが、本発明は、もとより下記実施例に限定されるものではなく、前、後記の趣旨に適合し得る範囲で適当に変更を加えて実施することも可能であり、それらはいずれも本発明の技術的範囲に含まれるものである。 Hereinafter, examples of the steel slab having a fine solidification structure according to the present invention will be given and the present invention will be described more specifically. However, the present invention is not limited to the following examples, and The present invention can be carried out with appropriate modifications within a range that can be adapted to the gist of the present invention, and these are all included in the technical scope of the present invention.
[サンプル作製]
下記表1に示す化学成分組成を有する10kg鋼鋳片を、実験室内に設置した真空溶解炉を用いて作製した。下記表1中、鋼Bと鋼28のみがγ−Fe凝固であり、その他の鋼は全てδ−Fe凝固である。また、鋳造の際は、溶鋼過熱度が60〜70℃になるように溶鋼温度を調整し、同一の鋳型(鋳型底面:約80mm四角、鋳型高さ:約200mm)を用いて鋳片を作製した。
[Sample preparation]
A 10 kg steel slab having the chemical composition shown in Table 1 below was produced using a vacuum melting furnace installed in a laboratory. In Table 1 below, only steel B and steel 28 are γ-Fe solidified, and the other steels are all δ-Fe solidified. During casting, the molten steel temperature is adjusted so that the molten steel superheat degree is 60 to 70 ° C., and a slab is produced using the same mold (mold bottom surface: about 80 mm square, mold height: about 200 mm). did.
[評価試験]
上記方法によって作製された鋳片の1/2高さ断面において、下記表1に示すCaX系酸化物の個数、等軸晶率、等軸晶粒径を測定し、結果を下記表2に示した。
[Evaluation test]
The number of CaX-based oxides, the equiaxed crystal ratio, and the equiaxed crystal grain size shown in Table 1 below were measured in a half height section of the slab produced by the above method, and the results are shown in Table 2 below. It was.
(CaX系酸化物の個数)
CaX系酸化物個数は、鋳片断面の中央部において次のような手順で測定した。まず、酸化物組成においてCaとXを同時に含有し、酸化物表面の全部あるいは一部が地鉄に直接接触しており、さらに、酸化物単独としての最大径が0.1〜10μmであることを満たす酸化物の個数を4mm2の面積にわたって測定し、1mm2あたりの個数に換算した。なお、この際、鋳片断面を研磨まで腐食することなく、WDSと走査型電子顕微鏡(SEM)を用いて上記の測定を行った。
(Number of CaX-based oxides)
The number of CaX-based oxides was measured by the following procedure at the center of the slab cross section. First, the oxide composition contains Ca and X at the same time, all or part of the oxide surface is in direct contact with the ground iron, and the maximum diameter of the oxide alone is 0.1 to 10 μm. The number of oxides satisfying the conditions was measured over an area of 4 mm 2 and converted to the number per 1 mm 2 . At this time, the above measurement was performed using WDS and a scanning electron microscope (SEM) without corroding the cross section of the slab until polishing.
酸化物組成のWDS測定では、検出されたFeを差し引き、さらにSが検出される場合にはこれと等量のCaを差し引き、Nが検出される場合にはこれと等量のXを差し引き、地鉄の影響や酸化物上のCaSやXNの影響を差し引くことで、可能な限り正確に酸化物組成を求めた。酸化物にCaSやXNが複合する場合には、SEM像や組成像を用いて酸化物、CaS、XNの存在形態を分離し、酸化物表面と地鉄の接触状況を判断すると同時に、酸化物の最大径を測定した。 In the WDS measurement of the oxide composition, the detected Fe is subtracted, and further, when S is detected, an equivalent amount of Ca is subtracted, and when N is detected, the same amount of X is subtracted. The oxide composition was determined as accurately as possible by subtracting the influence of the base iron and the influence of CaS and XN on the oxide. When CaS and XN are combined with the oxide, the presence of oxide, CaS, and XN is separated using SEM images and composition images, and at the same time the contact state between the oxide surface and the ground iron is judged, and the oxide The maximum diameter was measured.
なお、上述のような測定を4mm2の広い面積にわたって実行することが困難な場合、以下に説明するような簡便な測定方法に代替して測定を行った。
まず、任意に10個以上の酸化物粒子をSEM−WDS装置で解析し、酸化物組成、酸化物表面と地鉄との接触状況、酸化物の最大径を測定し、本発明で規定するCaX系酸化物の存在割合を求める。次に、WDSによるOのマッピング処理によって、4mm2の面積における酸化物個数を測定する。そして、面積1mm2当たりの酸化物個数にCaX系酸化物の存在割合をかけ合わせ、1mm2当たりのCaX系酸化物個数を求める。なお、このような酸化物分散状態の測定は、鋼鋳片とそれを加工した製品においてほぼ同じであるから、製品の任意断面で実行しても構わない。
In addition, when it was difficult to perform the above-described measurement over a wide area of 4 mm 2 , the measurement was performed instead of a simple measurement method as described below.
First, 10 or more oxide particles are arbitrarily analyzed with a SEM-WDS apparatus, the oxide composition, the contact state between the oxide surface and the ground iron, the maximum diameter of the oxide are measured, and the CaX defined in the present invention. The ratio of the system oxide is determined. Next, the number of oxides in an area of 4 mm 2 is measured by O mapping process using WDS. Then, the oxide quantity per area 1 mm 2 combined over existing ratio of CaX based oxide, obtaining the CaX based oxide number per 1 mm 2. In addition, since the measurement of such oxide dispersion | distribution state is substantially the same in the steel slab and the product which processed it, you may perform in the arbitrary cross sections of a product.
(等軸晶率及び等軸晶粒径)
等軸晶率及び等軸晶粒径は、鋼鋳片の1/2高さ断面をエッチプリント法で観察し、次の手順で測定した。
即ち、等軸晶率は、鋼鋳片の全断面における等軸晶部分の面積割合を測定した。
また、等軸晶粒径は、等軸晶部分のデンドライト方向が不連続に変化する境界を結晶粒界とみなし、最大径の大きい順に20個を測定して平均化した。
(Equiaxial crystal ratio and equiaxed crystal grain size)
The equiaxed crystal ratio and the equiaxed crystal grain size were measured by the following procedure after observing a half height section of the steel slab by the etch print method.
That is, the equiaxed crystal ratio was measured by measuring the area ratio of the equiaxed crystal portion in the entire cross section of the steel slab.
Further, the equiaxed crystal grain size was averaged by measuring 20 particles in order of increasing maximum diameter, considering the boundary where the dendrite direction of the equiaxed crystal part changes discontinuously as a crystal grain boundary.
本実施例の各鋼片の化学成分組成の一覧を表1に示し、また、各測定結果の一覧を表2に示す。 A list of chemical composition of each steel slab of this example is shown in Table 1, and a list of measurement results is shown in Table 2.
[評価結果]
表1に示す鋼A及び鋼1〜6、9〜13、15は本発明鋼であり、鋼成分とCaX系酸化物の分散状態が適正であるため、表2に示すように、本鋳造条件において等軸晶率が70%以上と高く、等軸晶粒径が1〜3mmと小さいことが確認された。
[Evaluation results]
Steel A and steel 1-6 shown in Table 1, 9 ~13,15 is the invention steels, since the dispersion state of the steel component and CaX based oxide is proper, as shown in Table 2, the present casting condition It was confirmed that the equiaxed crystal ratio was as high as 70% or more and the equiaxed crystal grain size was as small as 1 to 3 mm.
表1の鋼AA、鋼B及び鋼16〜32は比較鋼であり、この内、鋼AA、鋼B及び鋼16〜29はCaとXを添加したものであるが、化学成分やCaX系酸化物の分散状態が適正でないため、表2に示すように、本鋳造条件において等軸晶率が40%以下と本発明鋼よりも低く、等軸晶粒径が5〜8mmと本発明鋼よりも大きいことが確認された。
また、鋼29〜32は、CaとXを添加せずにREM、Ba、Mgを添加した比較鋼であり、等軸晶率が50〜60%と本発明鋼よりも低く、等軸晶粒径が4mmと本発明鋼よりも大きいことが確認された。
Steel AA, Steel B and Steels 16 to 32 in Table 1 are comparative steels, and Steel AA, Steel B and Steels 16 to 29 are those in which Ca and X are added. Since the dispersion state of the product is not appropriate, as shown in Table 2, the equiaxed crystal ratio is 40% or less, which is lower than the steel of the present invention, and the equiaxed grain size is 5-8 mm, which is smaller than the steel of the present invention. Was also confirmed to be large.
Steels 29 to 32 are comparative steels in which REM, Ba, and Mg are added without adding Ca and X, and the equiaxed crystal ratio is 50 to 60%, which is lower than that of the steel of the present invention. It was confirmed that the diameter was 4 mm, which was larger than the steel of the present invention.
なお、鋼30〜32と同様の化学成分を有する鋳片を製鋼工場(量産工場)で連続鋳造したところ、ノズル閉塞や元素低歩留などの問題が発生した。一方、本発明鋼を製鋼工場で連続鋳造した際には、ノズルの閉塞は発生せず、ZrやHfの歩留はCaのそれよりも高く、特段の問題は認められなかった。 In addition, when the slab which has the chemical composition similar to steel 30-32 was continuously cast in the steelmaking factory (mass production factory), problems, such as nozzle obstruction | occlusion and an element low yield, generate | occur | produced. On the other hand, when the steel according to the present invention was continuously cast in a steelmaking factory, nozzle clogging did not occur, the yield of Zr and Hf was higher than that of Ca, and no particular problem was observed.
以上説明した実施例の結果より、本発明の凝固組織が微細な鋼鋳片が、凝固組織の微細化を通じて偏析やポロシティが微細化され、従来よりも無害化される効果を有しており、延いては、鋳造欠陥の悪影響を軽減する目的で行われる負荷工程を軽減することができ、また、高機能化要求に対する鋳片起因の障害を取り除くことができることが明らかである。
From the results of the examples described above, the steel slab with a fine solidified structure of the present invention has an effect that the segregation and porosity are refined through refinement of the solidified structure, and is made harmless than before, As a result, it is clear that the loading process performed for the purpose of reducing the adverse effects of casting defects can be reduced, and that the obstacle caused by the slab for the demand for higher functionality can be removed.
Claims (2)
C :0.5%以下、
S :0.01%以下、
N :0.05%以下、
O :0.001〜0.01%、
Al:0.001〜0.1%、
Ca:0.0020〜0.005%
を含有し、さらに、
Zr:0.0005〜0.05%、
Hf:0.001〜0.1%
の内の1種又は2種を含有し、残部が鉄及び不可避的不純物からなり、凝固初相がδ−Feとなる鋼鋳片であって、
該鋼鋳片中の酸化物の内、Caと、Zr及びHfの内の1種又は2種とを同時に含み、その表面の全部又は一部が第三物質を介することなく地鉄に直接接触するように存在するとともに、0.1〜10μmの最大径を有するCaX系酸化物が、単独粒子あるいは複合粒子として、任意断面において面積1mm2当たりで1個以上存在することを特徴とする、凝固組織が微細な鋼鋳片。
但し、前記CaX系酸化物のXは、Zr及びHfの内の1種又は2種である。 The component composition of the steel slab is mass%,
C: 0.5% or less,
S: 0.01% or less,
N: 0.05% or less,
O: 0.001-0.01%,
Al: 0.001 to 0.1%,
Ca: 0.0020 to 0.005%
In addition,
Zr: 0.0005 to 0.05%,
Hf: 0.001 to 0.1%
A steel slab containing one or two of the above, the balance being iron and inevitable impurities, and the solidification initial phase being δ-Fe,
Of the oxides in the steel slab, it contains Ca and one or two of Zr and Hf at the same time, and all or part of the surface is in direct contact with the iron without passing through a third substance. And at least one CaX-based oxide having a maximum diameter of 0.1 to 10 μm is present as an individual particle or a composite particle per 1 mm 2 area in an arbitrary cross section. Steel slab with fine structure.
However, X of the CaX-based oxide is one or two of Zr and Hf.
Cr当量=Cr+Mo+1.5Si+0.5Nb+21.4Al+40B+8.29V ・・・(1)
Ni当量=Ni+30C+30N+0.5Mn+0.16Cu ・・・(2) Deoxidation force in the molten steel is smaller components than Al, Si, Mn, N b , V, Cu, Ni, Cr, Mo, as well as containing one or more of B, these components The Cr equivalent calculated by the following formula (1) is 30% by mass or less, and the Ni equivalent calculated by the following formula (2) is 15% by mass or less. A steel slab having a fine solidification structure according to claim 1.
Cr equivalent = Cr + Mo + 1.5Si + 0.5Nb + 21.4Al + 40B + 8.29V (1)
Ni equivalent = Ni + 30C + 30N + 0.5Mn + 0.16Cu (2)
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