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JP6809256B2 - Mold powder for continuous casting - Google Patents
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JP6809256B2 - Mold powder for continuous casting - Google Patents

Mold powder for continuous casting Download PDF

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JP6809256B2
JP6809256B2 JP2017014379A JP2017014379A JP6809256B2 JP 6809256 B2 JP6809256 B2 JP 6809256B2 JP 2017014379 A JP2017014379 A JP 2017014379A JP 2017014379 A JP2017014379 A JP 2017014379A JP 6809256 B2 JP6809256 B2 JP 6809256B2
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mold
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JP2018122312A (en
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山本 研一
研一 山本
仁巳 木村
仁巳 木村
和晃 三島
和晃 三島
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Nippon Steel Corp
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Description

本発明は、低炭素鋼(例えば質量%でCが0.0200〜0.0800%)やNb−Ti−SULC(極低炭素鋼、例えば質量%でCが0.0005〜0.0200%)に係る、高清浄飲料缶、高清浄自動車用大外板用等の高級鋼向け鋳片を連続鋳造する際に、好適に表面疵を防止し、表面品位の良好な鋳片を得ることを可能とする連続鋳造用モールドパウダーに関するものである。 The present invention relates to low carbon steel (for example, 0.0200 to 0.0800% C in mass%) and Nb-Ti-SULC (ultra-low carbon steel, for example 0.0005 to 0.0200% C in mass%). When continuously casting slabs for high-grade steel such as high-clean beverage cans and large outer panels for high-clean automobiles, it is possible to suitably prevent surface defects and obtain slabs with good surface quality. It relates to a mold powder for continuous casting.

低炭素鋼(例えば質量%でCが0.0200〜0.0800%)やNb−Ti−SULC(極低炭素鋼、例えば質量%でCが0.0005〜0.0200%)において連続鋳造を行う場合、鋳型と凝固シェル間の潤滑のためにパウダーを流入させる必要がある。また、パウダーの流入特性を向上させるためには、パウダーの低粘性化が必要である。一方、低炭素鋼やNb−Ti−SULC(極低炭素鋼)の表面割れ、表面疵を防止し、表面品位を向上させるためには、パウダー巻き込みの防止が重要で、そのためにパウダー中SiO2活量を小さくした低反応性化が行われている。このような厳しい制約の下に設計され、製造されているパウダーを使用してもなお、前記鋼種を鋼板とした場合、熱延板の筋状の疵や、鋼板を溶融亜鉛めっきした後の筋状の疵に係る課題が未だ解決できず、その中では、一部、パウダー成分中の特有成分に起因する疵も発生している。 Continuous casting in low carbon steel (eg 0.0200-0.0800% C in mass%) and Nb-Ti-SULC (eg very low carbon steel, eg 0.0005-0.0200% C in mass%) If so, it is necessary to inject powder for lubrication between the mold and the solidified shell. Further, in order to improve the inflow characteristics of the powder, it is necessary to reduce the viscosity of the powder. On the other hand, in order to prevent surface cracks and surface defects of low carbon steel and Nb-Ti-SULC (ultra-low carbon steel) and improve surface quality, it is important to prevent powder entrainment, and therefore SiO 2 in the powder. The reactivity is reduced by reducing the activity. Even if powder designed and manufactured under such strict restrictions is used, when the steel type is a steel plate, streaks on the hot-rolled plate and streaks after hot-dip galvanizing the steel plate are used. The problem related to the shape of the defect has not been solved yet, and some of the defects are caused by the peculiar component in the powder component.

上述の熱延板の筋状の疵、鋼板を溶融亜鉛めっきした後の筋状の疵は、鋳片から圧延板の表面近傍に存在する酸化物系非金属介在物やパウダー成分が、加熱炉における加熱時や引き続き行われる熱延、冷延時に、破砕したり、引き延ばされたりして鋼板の表面疵となるために発生する。この課題に対し、これまで問題となる非金属介在物やパウダーの成分を規定したり、モールド内での挙動を解明することで、表面疵を形成しない組成や、鋳造方法によって制御する方法等が採られてきた。 The above-mentioned streaky flaws on the hot-rolled plate and streaky flaws after hot-dip galvanizing the steel sheet are caused by oxide-based non-metal inclusions and powder components existing from the slab near the surface of the rolled plate in the heating furnace. It occurs because it is crushed or stretched and becomes a surface defect of the steel sheet during heating, subsequent hot rolling, and cold rolling. To solve this problem, by defining the components of non-metal inclusions and powders that have been problematic so far, and by clarifying the behavior in the mold, the composition that does not form surface defects, the method of controlling by the casting method, etc. It has been taken.

例えば、特許文献1や特許文献2には、パウダー中のP2O5を0.5%以下に制御することで、疵を低減できることが記載されたり、高SiO2濃度パウダーで、0.5-10%のCr2O3を含有し、モールド内で懸濁粒子として非ニュートン流体化する方法が記載されている。 For example, Patent Document 1 and Patent Document 2 describe that defects can be reduced by controlling P 2 O 5 in the powder to 0.5% or less, or 0.5-10 with a high SiO 2 concentration powder. A method of non-Newtonian fluidization as suspended particles in a mold containing% Cr 2 O 3 is described.

特願2016-100309号公報Japanese Patent Application No. 2016-100309 特許第5454131号公報Japanese Patent No. 5454131

しかしながら、特許文献1や特許文献2の技術を用いても、熱延板の筋状の疵、鋼板を溶融亜鉛めっきした後の筋状の疵を完全になくすことはできない。それは、単純なパウダー成分の規定だけでは対応し得ない、すなわち、溶鋼側の成分起因によるものや、0.5-10%のCr2O3を含有する高SiO2濃度パウダー使用によってモールド内で懸濁粒子として非ニュートン流体化するような物理的な操作だけでは対応し得ない要因に起因することもあるためである。 However, even if the techniques of Patent Document 1 and Patent Document 2 are used, it is not possible to completely eliminate the streaky flaws of the hot-rolled plate and the streak flaws after hot-dip galvanizing the steel plate. It cannot be dealt with by simply specifying the powder component, that is, it is suspended in the mold due to the component on the molten steel side or by using a high SiO 2 concentration powder containing 0.5-10% Cr 2 O 3. This is because it may be caused by factors that cannot be dealt with only by physical operations such as non-Newtonian fluidization as particles.

そこで本発明は、こうした背景を鑑みて、低炭素鋼やNb−Ti−SULC(極低炭素鋼)の連続鋳造を行う場合において、前述のような単純なパウダー成分規定や、モールド内懸濁粒子の物理的な操作(物理現象)等だけでは対応し切れない要因があっても、表面疵を防止し、表面品位の良好な鋳片を得ることを可能とするパウダーを考案し提供する。そのために、パウダー自身の成分変動が小さいばかりではなく、溶鋼成分変動が少なく、溶鋼成分によってパウダー成分の還元がないものとし、パウダーの成分を、溶鋼-パウダーの熱力学平衡分配の考え方を用いて設計、製造する。これにより、表面疵に起因する成分を溶鋼からパウダー側に移行させ無害化することができ、表面疵を防止して、表面品位の良好な鋳片を得るためのパウダーを提供することができる。 Therefore, in view of this background, the present invention defines the simple powder components as described above and the suspended particles in the mold when continuously casting low carbon steel or Nb-Ti-SULC (ultra-low carbon steel). Even if there are factors that cannot be dealt with only by the physical operation (physical phenomenon) of the above, we devise and provide a powder that can prevent surface defects and obtain slabs with good surface quality. Therefore, not only the component fluctuation of the powder itself is small, but also the molten steel component fluctuation is small, and the powder component is not reduced by the molten steel component, and the powder component is set using the concept of thermodynamic equilibrium distribution of molten steel-powder. Design and manufacture. Thereby, the component caused by the surface defect can be transferred from the molten steel to the powder side to make it harmless, and the powder for preventing the surface defect and obtaining a slab having good surface quality can be provided.

本発明者は、鋭意研究の結果、パウダーを使用することで発生している熱延板の筋状の疵、鋼板を溶融亜鉛めっきした後の筋状の疵は、単にパウダーだけの成分の問題や、物理現象では抑制できない溶鋼−パウダー間の化学反応に基づく現象であり、そうした2相の熱力学的化学平衡の理論を用いて抑制が可能となることを知見した。本発明においては、パウダー成分、なかでもパウダー中の特有成分に起因する疵を低減すべく、特に、鋼中のリン([P])、パウダー中のリン酸((P2O5))に起因する筋状の表面疵を防止しながら、高速鋳造を可能とする連続鋳造用パウダーを検討した。即ち、溶鋼-パウダーの熱力学的化学反応平衡分配の考え方を用いて、モールド内鋳造中のパウダーによる溶鋼の再酸化反応を起こさせない、もしくは、パウダーによる溶鋼の再酸化反応によって生じる鋼中のリン([P])を、溶鋼からパウダー側に移行させ無害化する。これにより、従来よりも、確実に熱延板の筋状の疵、鋼板を溶融亜鉛めっきした後の筋状の疵課題に対応し、高速鋳造を可能とする連続鋳造用パウダーが得られる。この考え方は、溶鋼-パウダーの化学反応平衡分配として、溶鋼中成分が、低Si、高Si、高Mn、高Al、高Ti、高Nbに対しても、応用していくことが可能になることを知見した。本発明は、このような知見に基づいて完成させた。尚、[P]の[ ]は溶鋼中の成分を示し、単位は質量%、(P2O5)の( )は、パウダー、スラグ中の酸化物成分を示し、単位は質量%である。 As a result of diligent research, the present inventor has found that the streaky flaws on the hot-rolled plate caused by the use of powder and the streaky flaws after hot-dip galvanizing the steel plate are problems of the components of the powder only. It was also found that it is a phenomenon based on a chemical reaction between molten steel and powder that cannot be suppressed by a physical phenomenon, and that it can be suppressed by using the theory of such two-phase thermodynamic chemical equilibrium. In the present invention, in order to reduce the flaws caused by the powder component, especially the peculiar component in the powder, in particular, phosphorus ([P]) in steel and phosphoric acid ((P 2 O 5 )) in powder are used. We investigated a powder for continuous casting that enables high-speed casting while preventing streaky surface flaws caused by it. That is, using the concept of thermodynamic chemical reaction equilibrium distribution of molten steel-powder, phosphorus in steel generated by the reoxidation reaction of molten steel by powder during casting in the mold is not caused. ([P]) is detoxified by shifting from molten steel to the powder side. As a result, it is possible to obtain a powder for continuous casting that enables high-speed casting by reliably dealing with the streak-like flaws of the hot-rolled plate and the streak-like flaws after hot-dip galvanizing the steel sheet. This idea can be applied to low Si, high Si, high Mn, high Al, high Ti, and high Nb as the chemical reaction equilibrium distribution of molten steel-powder. I found that. The present invention has been completed based on such findings. In addition, [] of [P] indicates the component in molten steel, the unit is mass%, () of (P 2 O 5 ) indicates the oxide component in powder and slag, and the unit is mass%.

本発明は、このような知見に基づいて完成したものである。本発明の要旨とするところは、以下のとおりである。 The present invention has been completed based on such findings. The gist of the present invention is as follows.

が質量%で0.0005%以上0.0800%以下の低炭素鋼、極低炭素鋼を連続鋳造する際に使用する連続鋳造用モールドパウダーであって、当該低炭素鋼、極低炭素鋼の成分の鋳片を連続鋳造する際に、鋳型内に供給するモールドパウダーの成分が、下記式(1)を満たすことを特徴とする連続鋳造用モールドパウダー。
([Si]×[P](4/5)×(Al2O3)(4/3))/((SiO2)×(P2O5)(2/5)×[Al](8/3))≧1.64 (1)
ここで、[Si]、[P]、[Al]]は溶鋼中の成分の質量%を示し、(Al2O3)、(SiO2)、(P2O5)は、鋳型内の溶融パウダーと溶鋼の界面の部分に分析サンプラーを装入して、サンプリングしたモールドパウダーの溶融物の酸化物成分の質量%である。
Mold powder for continuous casting used for continuous casting of low carbon steel and ultra-low carbon steel in which C is 0.0005% or more and 0.0800% or less in mass%, and the low carbon steel and ultra-low carbon steel. A mold powder for continuous casting, characterized in that the components of the mold powder supplied into the mold during continuous casting of the slabs of the above components satisfy the following formula (1).
([Si] × [P] (4/5) × (Al2O3) (4/3)) / ((SiO2) × (P2O5) (2/5) × [Al] (8/3)) ≧ 1.64 ( 1)
Here, [Si], [P], and [Al] indicate the mass% of the components in the molten steel, and (Al2O3), (SiO2), and (P2O5) are the portions of the interface between the molten powder and the molten steel in the mold. It is the mass% of the oxide component of the melt of the molded powder sampled by charging the analysis sampler.

本発明のパウダーを用いることによって、パウダー巻き込みによる表面割れ、疵を防止し、パウダー成分での特有成分に起因するもの疵を低減することができる。 By using the powder of the present invention, it is possible to prevent surface cracks and scratches due to powder entrainment, and to reduce scratches caused by peculiar components in the powder component.

式(1)と筋状模様発生率との関係を示すグラフである。It is a graph which shows the relationship between the equation (1) and the streak pattern occurrence rate. 本発明のパウダーの使用前と使用後の筋状模様発生率を示すグラフである。It is a graph which shows the streak pattern occurrence rate before use and after use of the powder of this invention.

発明者らは、低炭素鋼(極低炭素鋼含む)の表面品位向上のための、パウダー巻き込み防止の観点から多くの実験を行い、パウダーによる筋状の表面疵は、パウダーの巻き込みといった物理的な現象ではないことに思い至った。そこで本発明では、前述のように、特に鋼中のリン([P])、パウダー中のリン酸((P2O5))に起因して発生している熱延板の筋状の疵、鋼板を溶融亜鉛めっきした後の筋状の疵課題に対応するため、熱力学的に、化学反応を用いた新たな着想で、パウダー中へのりん含有能力を高めることに着想した。以下、詳細に説明する。 The inventors have conducted many experiments from the viewpoint of preventing powder entrainment in order to improve the surface quality of low carbon steel (including ultra-low carbon steel), and streaky surface flaws caused by powder are physical such as powder entrainment. I realized that it was not a normal phenomenon. Therefore, in the present invention, as described above, streaky flaws in the hot-dip galvanized sheet are particularly caused by phosphorus ([P]) in steel and phosphoric acid ((P 2 O 5 )) in powder. In order to deal with the problem of streaky flaws after hot-dip galvanizing a steel sheet, the idea was to increase the phosphorus content capacity in the powder by a new idea thermodynamically using a chemical reaction. The details will be described below.

低炭素鋼やNb−Ti−SULC(極低炭素鋼)において連続鋳造を行う場合、パウダーを使用することで発生していた熱延板の筋状の疵、鋼板を溶融亜鉛めっきした後の筋状の疵課題を解決するポイントは次のとおりである。りん[P]をパウダー中へ濃化させる(取り込む)考え方に対して、溶鋼-パウダー相においてPを分配させるという考え方を適用することに着想したのは前述の通りである。すなわち、りん分配比(P2O5)/[P]式で表せ、このP分配式を大きくすることを考えることに着想した。 When continuous casting is performed on low carbon steel or Nb-Ti-SULC (ultra-low carbon steel), the streaks of the hot-rolled plate that occur due to the use of powder and the streaks after hot-dip galvanizing the steel sheet The points to solve the problem of defects are as follows. As mentioned above, the idea of distributing P in the molten steel-powder phase was applied to the idea of concentrating (incorporating) phosphorus [P] into the powder. That is, it can be expressed by the phosphorus distribution ratio (P 2 O 5 ) / [P] equation, and the idea was to consider increasing this P distribution equation.

一方、溶鋼中の各成分とパウダー中の各成分とが酸化還元反応を起こして、各成分を溶鋼-パウダー相に分配することを考える。[P]の反応については、次の反応式(1)で示され、そのPの酸化還元反応に関わる成分を、[Al],[Si]と考えて、対応する反応を反応式(2)、(3)のように鋼中の[Al],[Si]の酸化還元反応で示すことが出来ると考えた。
(P2O5)→2[P]+5[O] (1)
2[Al]+3[O]→(Al2O3) (2)
[Si]+2[O]→(SiO2) (3)
この時、上式(1),(2),(3)に関わる[O]濃度が一定と仮定すると、(1),(2),(3)式を組み合わせることができ、次の式(4)を得ることができる。
(SiO2)+2/5(P2O5)+8/3[Al]→[Si]+4/5[P]+4/3(Al2O3) (4)
この式(4)は、関わる[O]濃度について一定であると仮定した場合のものであるが、今回、この反応式を(P2O5)/[P]式に応用することに着想した。式(4)を応用して、[Al],[Si]の項を加えて、次の式(5)を得て、この式(5)を応用P分配式として、今回の表面疵の指標として用いることを着想した。この式(5)を指標として用いる。
([Si]×[P](4/5)×(Al2O3)(4/3))/((SiO2)×(P2O5)(2/5)×[Al](8/3)) (5)
On the other hand, it is considered that each component in the molten steel and each component in the powder undergo a redox reaction to distribute each component to the molten steel-powder phase. The reaction of [P] is shown by the following reaction formula (1), and the components involved in the redox reaction of P are considered as [Al] and [Si], and the corresponding reaction is the reaction formula (2). , (3), it was thought that it could be shown by the redox reaction of [Al] and [Si] in steel.
(P 2 O 5 ) → 2 [P] + 5 [O] (1)
2 [Al] +3 [O] → (Al 2 O 3 ) (2)
[Si] +2 [O] → (SiO 2 ) (3)
At this time, assuming that the [O] concentration related to the above equations (1), (2), and (3) is constant, the equations (1), (2), and (3) can be combined, and the following equation ( 4) can be obtained.
(SiO 2 ) + 2/5 (P 2 O 5 ) + 8/3 [Al] → [Si] + 4/5 [P] + 4/3 (Al 2 O 3 ) (4)
This equation (4) is based on the assumption that the [O] concentration involved is constant, but this time, we came up with the idea of applying this reaction equation to the (P 2 O 5 ) / [P] equation. .. Applying equation (4), adding the terms [Al] and [Si], the following equation (5) is obtained, and this equation (5) is used as the applied P distribution equation, which is an index of surface defects this time. I was conceived to use it as. This equation (5) is used as an index.
([Si] × [P] (4/5) × (Al 2 O 3 ) (4/3) ) / ((SiO 2 ) × (P 2 O 5 ) (2/5) × [Al] (8) / 3) ) (5)

ここで、本発明において、[Si]、[P]、[Al]]は溶鋼中の各成分を質量%を示し、(Al2O3)、(SiO2)、(P2O5)は、鋳型内の溶融パウダーと溶鋼の界面の部分に分析サンプラーを装入して、サンプリングしたモールドパウダーの溶融物の酸化物成分の質量%である。 Here, in the present invention, [Si], [P], and [Al] indicate the mass% of each component in the molten steel, and (Al 2 O 3 ), (SiO 2 ), and (P 2 O 5 ) are. , The mass% of the oxide component of the melt of the molded powder sampled by charging the analysis sampler at the interface between the molten powder and the molten steel in the mold.

こうして、この式(5)を用いて、鋳片が最終製品の鋼板のコイルとなったときの、コイル当たりの表面疵の発生率を縦軸に整理すると、図1に示すように、1.64を境に、表面疵の発生率を0に抑制できる領域を得て、本発明を成立させるに至った。 In this way, using this equation (5), when the slab becomes the coil of the steel plate of the final product, the incidence of surface defects per coil is arranged on the vertical axis. As shown in FIG. 1, 1.64 is obtained. At the boundary, a region in which the incidence of surface defects can be suppressed to 0 was obtained, and the present invention was established.

上式(4)によって、(SiO2)活量(濃度)、(P2O5)活量(濃度)、(Al2O3)活量(濃度)をそれぞれ、下げる、下げる、上げることが、Pをパウダーに取り込むことに有効であると考えることができる。すなわち、Pを取り込むということだけを考えるならば、(SiO2)=0、(P2O5)=0、(Al2O3)=大とすることが望ましいが、それではパウダーとしての通常の潤滑、保温の為の必要な粘性、凝固温度等を満足せず、パウダーとしての機能を果たせない。そのために、式(5)の1.64以下の範囲の中で、通常の潤滑、保温の為に必要な粘性、凝固温度等を満足するような通常のパウダーの設計を合わせて考えることが必要である。すなわち、通常のパウダーの潤滑、保温、粘性、凝固温度を得る中で、式(5)=<1.64を満たすパウダーを設計することができ、粘性、凝固温度については、本発明では特に規定しないが、通常のパウダーとしての好ましい条件としては、1300℃における粘性が、0.5〜20poise, 凝固温度は、1000〜1300℃である。 According to the above equation (4), (SiO 2 ) activity (concentration), (P 2 O 5 ) activity (concentration), and (Al 2 O 3 ) activity (concentration) can be lowered, lowered, or raised, respectively. , P can be considered to be effective in incorporating into powder. That is, if only considering the uptake of P, it is desirable to set (SiO 2 ) = 0, (P 2 O 5 ) = 0, (Al 2 O 3 ) = large, but then it is normal as a powder. It does not satisfy the viscosity required for lubrication and heat retention, solidification temperature, etc., and cannot function as a powder. Therefore, it is necessary to consider the design of a normal powder that satisfies the normal lubrication, the viscosity required for heat retention, the solidification temperature, etc. within the range of 1.64 or less in the formula (5). .. That is, it is possible to design a powder satisfying the equation (5) = <1.64 while obtaining the lubrication, heat retention, viscosity, and solidification temperature of a normal powder, and the viscosity and solidification temperature are not particularly specified in the present invention. As a normal powder, the viscosity at 1300 ° C. is 0.5 to 20 poise, and the solidification temperature is 1000 to 1300 ° C.

本発明により鋳造された鋳片は、その後圧延等がされて自動車用薄鋼板、自動車用部材、もしくは低炭素熱延鋼板に用いられる。本発明の鋳片の成分は、例えば質量%で、
C:0.0005〜0.0800%、
Si:0.01〜1.00%、
Mn:0.10〜1.00%、
P:0.0500%以下、
S:0.0100%以下、
T.O:0.0040%以下、
N:0.0005〜0.0100%
酸可溶Al:0.003〜0.130%、
酸可溶Ti:0.0050〜0.1000%、
Nb:0.0050〜0.1000%、
残Feおよび不可避的不純物で、選択元素としてCr,Mo,V,W,B、Ca,REMCu、Ni、Zrを含有する場合がある。本発明に係る鋳片や鋼板の主成分について、以下に説明する。単位は、特に説明が無い場合には、いずれも質量%である。
The slab cast according to the present invention is subsequently rolled or the like and used for an automobile thin steel sheet, an automobile member, or a low carbon hot-rolled steel sheet. The components of the slab of the present invention are, for example,% by mass.
C: 0.0005-0.0800%,
Si: 0.01-1.00%,
Mn: 0.10 to 1.00%,
P: 0.0500% or less,
S: 0.0100% or less,
T. O: 0.0040% or less,
N: 0.0005 to 0.0100%
Acid-soluble Al: 0.003 to 0.130%,
Acid-soluble Ti: 0.0050 to 0.1000%,
Nb: 0.0050 to 0.1000%,
Residual Fe and unavoidable impurities, which may contain Cr, Mo, V, W, B, Ca, REMCu, Ni, and Zr as selective elements. The main components of the slab and the steel plate according to the present invention will be described below. Unless otherwise specified, the unit is mass%.

<C:0.0005〜0.0800%>
Cは、低炭素鋼や、IF鋼の加工性、鋼の焼入れ性と強度を制御する最も基本的な元素であり、必要な強度を確保しつつ、良好な加工性を高めることに有効に寄与する。即ち、Cは、鋼板の強度と、良好な加工性を両立するために必須の元素であり、良好な加工性を得るためには、少なくとも0.005%が含まれていることが好ましく、より好ましくは、0.002%以上である。一方、Cが0.0800%を超えると、粗大な初析セメンタイト組織が多量に生成し、加工性が低下するので、必要な加工性を確保するため、Cは0.08%以下とすることが好ましい。
<C: 0.0005 to 0.0800%>
C is the most basic element that controls the workability, hardenability and strength of low carbon steel and IF steel, and effectively contributes to improving good workability while ensuring the required strength. To do. That is, C is an element essential for achieving both the strength of the steel sheet and good workability, and in order to obtain good workability, it is preferably contained at least 0.005%. Preferably, it is 0.002% or more. On the other hand, if C exceeds 0.0800%, a large amount of coarse protophilic cementite structure is generated and the workability is lowered. Therefore, in order to secure the necessary workability, C should be 0.08% or less. Is preferable.

<Si:0.01〜1.00%>
Siは、主要な脱酸元素の一つであり、焼入れ加熱時に、オーステナイトの核生成サイト数を増加させ、オーステナイトの粒成長を抑制するとともに、焼入れ硬化層の粒径を微細化する機能を担う。また、Siは、炭化物の生成を抑制し、炭化物による粒界強度の低下を抑制するとともに、ベイナイト組織の生成に対しても有効であるので、伸びを大きく損なうことなく強度を高め、低降伏強度比で穴拡げ性、曲げ加工性を改善するのに重要な元素である。
<Si: 0.01 to 1.00%>
Si is one of the main deoxidizing elements, and has the function of increasing the number of austenite nucleation sites during quenching and heating, suppressing the grain growth of austenite, and refining the particle size of the quenching hardened layer. .. Further, Si suppresses the formation of carbides, suppresses the decrease in grain boundary strength due to carbides, and is also effective for the formation of bainite structure, so that the strength is increased without significantly impairing the elongation and the yield strength is low. It is an important element for improving hole expansion and bending workability.

本実施形態では、パウダー中のSiO系成分との熱力学的反応平衡に関わってくるので、重要な元素である。パウダー中のSiO系成分を、Alで還元して、アルミナ系介在物、もしくは、パウダー中のAl成分を生成する。溶鋼中の溶存酸素濃度を低下させ、一旦、SiO系介在物を生成させるためには、Siを0.01%以上添加する必要があるので、Siの下限を0.01%とすることが好ましい。一方、Si濃度が高すぎると、介在物中のSiO濃度が高くなって、パウダーによって、酸化反応が生成し易くなり、Alによる還元が起こり難くなる。また、これにより表面疵が増加する。これに加え、過剰のSiは、良加工性、溶接性や延性に悪影響を及ぼし、成形性を劣化させるので、Siの上限を1.00%とすることが好ましい。 In this embodiment, it is an important element because it is involved in the thermodynamic reaction equilibrium with the SiO 2 system component in the powder. The SiO 2 component in the powder is reduced with Al to produce alumina-based inclusions or the Al 2 O 3 component in the powder. Since it is necessary to add 0.01% or more of Si in order to reduce the dissolved oxygen concentration in the molten steel and once generate SiO 2 inclusions, the lower limit of Si can be set to 0.01%. preferable. On the other hand, if the Si concentration is too high, the SiO 2 concentration in the inclusions becomes high, the powder easily causes an oxidation reaction, and reduction by Al is less likely to occur. This also increases surface flaws. In addition to this, excess Si adversely affects good workability, weldability and ductility, and deteriorates moldability. Therefore, it is preferable to set the upper limit of Si to 1.00%.

<Mn:0.10〜1.00%>
Mnは、製鋼段階での脱酸に有用な元素であり、C、Siとともに、鋼板の高強度化に有効な元素である。この効果を得るためには、0.10%以上含有させることが好ましい。より高強度の鋼板を得るには、0.15%以上とすることが一層好ましい。しかし、1.00%を超えて含有させると、Mnの偏析や固溶強化の増大により、延性が低下する。また、加工性、溶接性や母材靭性も劣化するので、Mnの上限を1.00%とすることが好ましい。
<Mn: 0.10 to 1.00%>
Mn is an element useful for deoxidation in the steelmaking stage, and together with C and Si, is an element effective for increasing the strength of steel sheets. In order to obtain this effect, it is preferable to contain 0.10% or more. In order to obtain a steel sheet having higher strength, it is more preferably 0.15% or more. However, if it is contained in excess of 1.00%, the ductility is lowered due to the segregation of Mn and the increase in solid solution strengthening. Further, since workability, weldability and base metal toughness are also deteriorated, it is preferable to set the upper limit of Mn to 1.00%.

<P:0.0500%以下>
Pは、Fe原子よりも小さく、置換型固溶強化元素として作用するので、強度の向上に有効な元素である。しかし、0.0500%を超えると、オーステナイトの粒界に偏析し、粒界強度を低下させて、ねじり疲労強度が低下し、加工性が劣化する原因にもなるので、上限を0.0500%とすることが好ましい。しかし、固溶強化の必要がなければ、Pを添加する必要はないので、Pの下限値は0.0000%を含むものとする。
<P: 0.0500% or less>
Since P is smaller than the Fe atom and acts as a substitution type solid solution strengthening element, it is an element effective for improving the strength. However, if it exceeds 0.0500%, segregation occurs at the grain boundaries of austenite, the grain boundary strength is lowered, the torsional fatigue strength is lowered, and the workability is deteriorated. Therefore, the upper limit is 0.0500%. Is preferable. However, if there is no need for solid solution strengthening, it is not necessary to add P, so the lower limit of P is assumed to include 0.0000%.

<S:0.0100%以下>
Sは、不純物として偏析して、MnS系の粗大な延伸介在物を形成して、加工性や材質特性を劣化させる。また、こうした悪影響を低減するために、極力、低濃度であることが望ましく、通常、精錬段階で低減するほか、Ca添加等を行う場合もある。このCa添加によって生成されるCaSやCaO−Al介在物は、加工性、溶接部の加工性に悪影響を与えるため、Sは更に低濃度であることが望ましい。しかし、本実施形態においては、表面疵への影響は無視できるので、Sを0.0100%以下とすることが可能である。それゆえ、本実施形態では、表面疵への影響は無視できるものの、加工性等の材質への悪影響を防止するあるいは、極限的な材質の向上を得るために、Sは、0.0070%以下とすることが好ましい。下限は、特に定める必要はないが、二次精錬を強化して脱硫を行った場合において実現可能な量としては、0.0001%である。
<S: 0.0100% or less>
S segregates as an impurity to form MnS-based coarse stretch inclusions, which deteriorates processability and material properties. Further, in order to reduce such an adverse effect, it is desirable that the concentration is as low as possible, and usually, in addition to reducing at the refining stage, Ca may be added or the like. CaS and CaO-Al 2 O 3 inclusions produced by the Ca addition, workability, because an adverse effect on workability of the weld, S is desirably a further lower concentration. However, in the present embodiment, since the influence on the surface defect can be ignored, S can be set to 0.0100% or less. Therefore, in the present embodiment, although the influence on the surface defect can be ignored, S is 0.0070% or less in order to prevent adverse effects on the material such as workability or to obtain the ultimate improvement in the material. Is preferable. The lower limit does not need to be set in particular, but the amount that can be realized when desulfurization is performed by strengthening the secondary refining is 0.0001%.

<T.O:0.0040%以下>
酸素は、不純物として酸化物を形成する。質量ベースの全酸素量T.Oが高すぎる場合、主としてAl系介在物が増大し、系の酸素ポテンシャルを極小にすることができなくなり、延性、加工性が極端に悪くなり、表面疵の増加に繋がる。このため、本実施形態においては、質量ベースの全酸素量T.Oの上限を0.0040%とすることが好ましい。
<T. O: 0.0040% or less>
Oxygen forms oxides as impurities. Mass-based total oxygen content T.I. When O is too high, mainly Al 2 O 3 system inclusions increase, the oxygen potential of the system cannot be minimized, ductility and workability become extremely poor, leading to an increase in surface defects. Therefore, in the present embodiment, the mass-based total oxygen amount T.I. The upper limit of O is preferably 0.0040%.

<N:0.0005〜0.0100%>
Nは、溶鋼処理中に空気中の窒素が取り込まれることから、鋼中に不可避的に混入する元素である。Nは、Al等と窒化物を形成して母材組織の細粒化を促進する。しかしながら、このNは0.0100%を超えて含有すると、Al等と粗大な析出物を生成し、加工性や材質特性、靭性を劣化させる。このため、本実施形態においては、Nの濃度の上限を0.0100%とすることが好ましい。より好ましいNの濃度の上限は、0.005%である。一方、Nの濃度を0.0005%未満とするにはコストが高くなるので、工業的に実現可能な観点から0.0005%を下限とすることが好ましい。
<N: 0.0005 to 0.0100%>
N is an element that is inevitably mixed in the steel because nitrogen in the air is taken in during the molten steel treatment. N forms a nitride with Al or the like to promote fine graining of the base metal structure. However, if this N is contained in an amount of more than 0.0100%, coarse precipitates such as Al are formed, and the processability, material properties, and toughness are deteriorated. Therefore, in the present embodiment, the upper limit of the concentration of N is preferably 0.0100%. The upper limit of the more preferable concentration of N is 0.005%. On the other hand, since the cost is high to make the concentration of N less than 0.0005%, it is preferable to set 0.0005% as the lower limit from the viewpoint of industrial feasibility.

<酸可溶Al:0.003〜0.130%>
酸可溶Alは一般的には、その酸化物がクラスター化して粗大になり易く、粗大Alが多数存在すると、靭延性が極端に悪くなり、表面疵が増加し、種々の材質を劣化させるため極力抑制することが望ましい。しかしながら、本発明者は、Al脱酸を行い、表面疵形成に関与する元素で重要である。このため、本実施形態においては、従来のようにアルミナ系酸化物の粗大なクラスターを避けるために実質的にAlを添加しないという制限を設ける必要もなくなり、特にこの酸可溶Alの濃度に関して自由度を高くしながら、表面疵を防止するための制御が可能となる。また、積極的に酸可溶Alを0.003%以上とすることにより、鋼中の酸素ポテンシャルを低く抑える効果を享受できる。酸可溶Al濃度を0.01%超とすることでこの効果はより顕著となる。
<Acid-soluble Al: 0.003 to 0.130%>
In general, acid-soluble Al tends to be coarse due to clustering of its oxide, and when a large number of coarse Al 2 O 3 are present, ductility is extremely deteriorated, surface defects are increased, and various materials are used. It is desirable to suppress it as much as possible because it deteriorates. However, the present inventor is important as an element involved in the formation of surface defects by performing Al deoxidation. Therefore, in the present embodiment, it is not necessary to set a restriction that Al is substantially not added in order to avoid coarse clusters of alumina-based oxides as in the conventional case, and the concentration of the acid-soluble Al is particularly free. It is possible to control to prevent surface defects while increasing the degree. Further, by positively adjusting the acid-soluble Al to 0.003% or more, the effect of suppressing the oxygen potential in the steel can be enjoyed. This effect becomes more remarkable when the acid-soluble Al concentration exceeds 0.01%.

高Al濃度により、耐食性も向上する。その効果の上昇代と添加コストの面から、酸可溶Al濃度は0.130%以下とすることが好ましい。また、ここでいう酸可溶Al濃度とは、酸に溶解したAlの濃度を測定したもので、溶存Alは酸に溶解し、Al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(質量比)で混合した混酸が例示できる。この様な酸を用いて、酸に可溶なAlと、酸に溶解しないAlとに分別でき、酸可溶Al濃度を測定できる。 Corrosion resistance is also improved due to the high Al concentration. The acid-soluble Al concentration is preferably 0.130% or less from the viewpoint of increasing the effect and the addition cost. Further, the acid-soluble Al concentration referred to here is a measurement of the concentration of Al dissolved in an acid, and is an analysis method utilizing the fact that dissolved Al is dissolved in acid and Al 2 O 3 is not dissolved in acid. is there. Here, as the acid, for example, a mixed acid in which hydrochloric acid 1, nitric acid 1, and water 2 are mixed in a ratio (mass ratio) can be exemplified. By using such an acid, Al soluble in acid and Al 2 O 3 insoluble in acid can be separated, and the concentration of acid-soluble Al can be measured.

<酸可溶Ti:0.0050〜0.1000%>
Tiは、主要な脱酸元素の一つであるとともに、炭化物、窒化物、炭窒化物を形成し、熱間圧延前の充分な加熱により、オーステナイトの核生成サイト数を増加し、オーステナイトの粒成長を抑制するための微細化・高強度化に寄与し、熱間圧延時の動的再結晶に有効に作用する機能を担う元素である。
上記機能を確保するには、酸可溶Tiを0.0050%以上添加する必要があることを、本発明者らは実験的に知見した。それ故、酸可溶Tiの下限を0.0050%とした。好ましい酸可溶Tiの下限は、0.010%である。
一方、酸可溶Tiを0.1000%を超えて含有すると、脱酸効果が飽和するのみならず、熱間圧延前に充分な加熱を行っても、粗大な炭化物、窒化物、炭窒化物が生成してしまい、かえって、材質の劣化を招き、含有量に見合う効果が期待できないので、上限を0.1000%とする。
ちなみに、酸可溶Ti濃度とは、酸に溶解したTiの濃度を測定したもので、溶存Tiは酸に溶解し、Ti酸化物は酸に溶解しないことを利用して分析、定量する。ここで、酸として、例えば、塩酸1、硝酸1、水2の割合(質量比)で混合した混酸を使用することができる。この酸を用いて、酸に可溶なTiと、酸に溶解しないTi酸化物を分別して、酸可溶Ti濃度を測定する。
<Acid-soluble Ti: 0.0050 to 0.1000%>
Ti is one of the major deoxidizing elements, forms carbides, nitrides, and carbonitrides, and by sufficient heating before hot rolling, it increases the number of austenite nucleation sites and austenite grains. It is an element that contributes to miniaturization and high strength to suppress growth and has a function of effectively acting on dynamic recrystallization during hot rolling.
The present inventors have experimentally found that it is necessary to add 0.0050% or more of acid-soluble Ti in order to secure the above function. Therefore, the lower limit of acid-soluble Ti was set to 0.0050%. The lower limit of preferred acid-soluble Ti is 0.010%.
On the other hand, if the acid-soluble Ti is contained in excess of 0.1000%, not only the deoxidizing effect is saturated, but also coarse carbides, nitrides and carbonitrides are produced even if sufficient heating is performed before hot rolling. Is generated, and on the contrary, the material is deteriorated and the effect commensurate with the content cannot be expected. Therefore, the upper limit is set to 0.1000%.
Incidentally, the acid-soluble Ti concentration is a measurement of the concentration of Ti dissolved in an acid, and is analyzed and quantified by utilizing the fact that dissolved Ti is dissolved in an acid and Ti oxide is not dissolved in an acid. Here, as the acid, for example, a mixed acid in which hydrochloric acid 1, nitric acid 1, and water 2 are mixed in a ratio (mass ratio) can be used. Using this acid, Ti soluble in acid and Ti oxide insoluble in acid are separated, and the acid-soluble Ti concentration is measured.

<Nb:0.0050〜0.1000%>、
Nbは、CまたはNと炭化物、窒化物、炭窒化物を形成して、母材組織の細粒化を促進し、靭性の向上に寄与する元素である。Nbを0.0050%以上添加する必要があることを、本発明者らは実験的に知見した。それ故、Nbの下限を0.0050%とした。好ましいNbの下限は、0.010%である。上述した炭化物、窒化物等を得るため、Nbを添加するのが好ましい。しかし、Nbの添加量がそれぞれ0.1000%を超えると、母材組織の細粒化効果が飽和し、製造コストが高くなるので、上限は0.1000%とする。
<Nb: 0.0050 to 0.1000%>,
Nb is an element that forms carbides, nitrides, and carbonitrides with C or N to promote fine graining of the base metal structure and contribute to improvement of toughness. The present inventors have experimentally found that it is necessary to add 0.0050% or more of Nb. Therefore, the lower limit of Nb was set to 0.0050%. The preferred lower limit of Nb is 0.010%. It is preferable to add Nb in order to obtain the above-mentioned carbides, nitrides and the like. However, if the amount of Nb added exceeds 0.1000%, the effect of atomizing the base metal structure is saturated and the production cost increases, so the upper limit is set to 0.1000%.

残Feおよび不可避的不純物で、選択元素としてCr,Mo,V,W,B、Ca,REMを含有する場合がある。 Residual Fe and unavoidable impurities, which may contain Cr, Mo, V, W, B, Ca, and REM as selective elements.

Cr、Mo,V,W,Bについては、鋼の強度を向上し鋼の焼き入れ性を向上する元素であり添加することができる。これらの元素は選択元素であるから、添加の有無は任意であり、必要に応じて1種だけ加えてもよく、2種以上加えてもよい。ただし、上述した炭化物、窒化物等を得るため、必要に応じて添加する。この添加効果を得るためには、各選択元素、0.01%以上添加することが好ましい。しかし、これらの元素の多量添加は、かえって、強度−延性バランスを劣化させるので、上限を0.10%とする。 Cr, Mo, V, W, and B are elements that improve the strength of steel and the hardenability of steel and can be added. Since these elements are selective elements, the presence or absence of addition is arbitrary, and only one type may be added or two or more types may be added as needed. However, in order to obtain the above-mentioned carbides, nitrides and the like, they are added as necessary. In order to obtain this addition effect, it is preferable to add 0.01% or more of each selected element. However, the addition of a large amount of these elements deteriorates the strength-ductility balance, so the upper limit is set to 0.10%.

B:0.0002〜0.0020%
Bは、さらに、粒界を強化し、加工性を向上するため、必要に応じて添加する。この効果を得るためには、0.0002%以上添加することが好ましい。しかし、Bを、0.0020%を超えて添加しても、添加効果は飽和し、かえって、鋼の清浄性を損ない、延性を劣化させるので、上限を0.0020%とする。
B: 0.0002 to 0.0020%
B is added as needed in order to further strengthen the grain boundaries and improve workability. In order to obtain this effect, it is preferable to add 0.0002% or more. However, even if B is added in an amount exceeding 0.0020%, the effect of addition is saturated, and on the contrary, the cleanliness of the steel is impaired and the ductility is deteriorated. Therefore, the upper limit is set to 0.0020%.

Ca:0.0005〜0.0050%
Caは、Sを固定し、介在物を形成させるための重要な元素である。 また、Caは、硫化物を球状化する等、脱硫の形態を制御することにより、粒界を強化し、鋼の加工性を向上する元素である。この効果を得るために、Caを0.0005%以上添加する。しかし、Caを多量に添加しても、添加効果は飽和し、かえって、鋼の清浄性を損ない、延性を劣化させるので、上限を0.0050%とする。
Ca: 0.0005 to 0.0050%
Ca is an important element for fixing S and forming inclusions. Further, Ca is an element that strengthens grain boundaries and improves the workability of steel by controlling the form of desulfurization such as spheroidizing sulfide. To obtain this effect, 0.0005% or more of Ca is added. However, even if a large amount of Ca is added, the effect of addition is saturated, and the cleanliness of the steel is impaired and the ductility is deteriorated. Therefore, the upper limit is set to 0.0050%.

REM:0.0005〜0.0100%
REMは、Si脱酸で生成したSiO2、逐次的にAl脱酸で生成したAl23を還元し、MnS系介在物の析出サイトとなり易く、かつ、硬質、微細で、圧延時に変形し難い介在物、すなわち、Ce酸化物(例えば、Ce23、CeO2)、セリュウムオキシサルファイド(例えば、Ce22S)、La酸化物(例えば、La23、LaO2)、ランタンオキシサルファイド(例えば、La22S)、Ce酸化物−La酸化物、および/または、セリュウムオキシサルファイド−ランタンオキシサルファイドを主相(50%以上を目安とする)とする介在物を形成する機能を備える元素であるため有効であり、添加することが出来る。
REMが0.0005%未満であると、SiO2およびAl23介在物を還元できず、一方、0.0100%超では、セリュウムオキシサルファイドや、ランタンオキシサルファイドが多量に生成し、いずれの条件でも、低酸素ポテンシャルを達成できず、さらには、粗大な介在物となり低温靭性を劣化させる。好ましいREMの下限は、0.0010%である。また、好ましいREMの上限は、0.0085%である。
REM: 0.0005-0.0100%
REM reduces SiO 2 generated by Si deoxidation and Al 2 O 3 generated by Al deoxidation sequentially, and easily becomes a precipitation site of MnS-based inclusions, and is hard and fine, and deforms during rolling. Difficult inclusions, ie Ce oxides (eg Ce 2 O 3 , CeO 2 ), cerium oxysulfide (eg Ce 2 O 2 S), La oxides (eg La 2 O 3 , La O 2 ), Lantern oxysulfide (for example, La 2 O 2 S), Ce oxide-La oxide, and / or inclusions containing cerium oxysulfide-lanthanum oxysulfide as the main phase (within 50% or more as a guide). Since it is an element having a function of forming, it is effective and can be added.
If the REM is less than 0.0005%, SiO 2 and Al 2 O 3 inclusions cannot be reduced, while if it exceeds 0.0100%, a large amount of cerium oxysulfide and lanthanum oxysulfide are produced. Even under the above conditions, the low oxygen potential cannot be achieved, and further, it becomes a coarse inclusion and deteriorates the low temperature toughness. The preferred lower limit of REM is 0.0010%. The upper limit of the preferable REM is 0.0085%.

Cu、Ni、Zrについて
本発明では、鋼の強度を向上し鋼の焼き入れ性を向上する元素であるCu、Ni、Crや、Zrをさらに添加することができる。これらの元素は選択元素であるから、添加の有無は任意であり、必要に応じて1種だけ加えてもよく、2種以上加えてもよい。以下、選択元素の限定理由について説明をする。
Cu, Ni, Zr In the present invention, Cu, Ni, Cr, and Zr, which are elements that improve the strength of steel and the hardenability of steel, can be further added. Since these elements are selective elements, the presence or absence of addition is arbitrary, and only one type may be added or two or more types may be added as needed. The reasons for limiting the selected elements will be described below.

Cu:0.10〜2.00%
Cuは、フェライトの析出強化や疲労強度向上に寄与し、さらに鋼板の強度を確保するために、必要に応じて含有することができ、この効果を得るためには0.10%以上添加することが好ましい。しかし、このCuの多量の含有はかえって強度−延性のバランスを劣化させる。そのため、2.00%を上限とする。
Cu: 0.10 to 2.00%
Cu can be contained as necessary in order to contribute to strengthening the precipitation of ferrite and improving fatigue strength, and further to secure the strength of the steel sheet, and in order to obtain this effect, 0.10% or more should be added. Is preferable. However, the inclusion of a large amount of this Cu rather deteriorates the strength-ductility balance. Therefore, the upper limit is 2.00%.

Ni:0.05〜1.00%
Niは、フェライトの固溶強化することができるため、さらに鋼板の強度を確保するために、必要に応じて含有することができ、この効果を得るためには0.05%以上添加することが好ましい。しかし、このNiの多量の含有はかえって強度−延性のバランスを劣化させる。そのため、1.00%を上限とする。
Ni: 0.05 to 1.00%
Since Ni can be solid-solved and strengthened of ferrite, it can be contained as needed in order to further secure the strength of the steel sheet, and 0.05% or more may be added to obtain this effect. preferable. However, the inclusion of a large amount of Ni rather deteriorates the strength-ductility balance. Therefore, the upper limit is 1.00%.

Zr:0.001〜0.010%
Zrは、硫化物を球状化して、母材の靭性を改善する効果を有する元素である。この効果を得るためには、0.001%以上添加することが好ましい。しかし、Zrの多量添加は、かえって、鋼の清浄性を損ない、延性を劣化させるので、上限を0.010%とする。
Zr: 0.001 to 0.010%
Zr is an element that has the effect of spheroidizing sulfide and improving the toughness of the base metal. In order to obtain this effect, it is preferable to add 0.001% or more. However, the addition of a large amount of Zr impairs the cleanliness of the steel and deteriorates the ductility, so the upper limit is set to 0.010%.

この溶鋼成分は、鋳造中にタンディッシュでサンプリングした溶鋼をスパーク発光分光分析(カントバック:KANT BACK、QV)もしくは化学分析によって求めた分析値である。モールドパウダーの成分は、鋳造中の鋳型内の溶鋼上にモールドパウダーを供給し、鋳型と溶鋼の界面の部分に分析サンプラーを装入して、サンプリングしたモールドパウダーの溶融物を、ガラスビード法によって、発光分析法で分析して求めた。 This molten steel component is an analytical value obtained by spark emission spectroscopic analysis (KANT BACK, QV) or chemical analysis of molten steel sampled in a tundish during casting. For the components of the mold powder, the mold powder is supplied onto the molten steel in the mold during casting, an analytical sampler is charged at the interface between the mold and the molten steel, and the sampled melt of the mold powder is subjected to the glass bead method. , Obtained by analysis by luminescence analysis method.

本発明を要約すると以下の通りとなる。
(1)鋼-パウダーの熱力学反応平衡分配の考え方を用いて、パウダーによる溶鋼の再酸化反応によって生じる鋼中のリン([P])を、溶鋼からパウダー側に取り込む(移行させる)、また[P]取り込み能力を大きくする
(2)パウダー中SiO2活量を小さくし低反応性化(再酸化反応防止)し、パウダーによる溶鋼の再酸化反応によって生じる鋼中のリン([P])をなくす(低減する)
(3)鋳型と凝固シェル間の潤滑のために、パウダーの流入特性を向上させる低粘性化
以上により、疵、欠陥の無害化、潤滑性の確保、パウダー巻き込みを防止しつつ高速鋳造を可能とする連続鋳造用パウダーとなる。最も重要なポイントは、(1)であり、(2)は低炭素鋼や極低炭素鋼におけるパウダー設計のこれまでの考え方に基づくものの、Pを還元しないように反応を制御する。(3)は、従来の発想に基づく考え方であり、本発明においては、好ましい条件である。
The present invention can be summarized as follows.
(1) Thermodynamic reaction of steel-powder Using the concept of equilibrium distribution, phosphorus ([P]) in steel generated by the reoxidation reaction of molten steel by powder is taken in (transferred) from molten steel to the powder side. [P] Increase the uptake capacity (2) Decrease the SiO 2 activity in the powder to reduce the reactivity (prevent the reoxidation reaction), and phosphorus ([P]) in the steel generated by the reoxidation reaction of the molten steel by the powder. Eliminate (reduce)
(3) Low viscosity to improve powder inflow characteristics for lubrication between mold and solidified shell. Detoxification of flaws and defects, ensuring lubricity, and high-speed casting while preventing powder entrainment are possible. It becomes a powder for continuous casting. The most important points are (1), and (2) is based on the conventional concept of powder design in low carbon steel and ultra-low carbon steel, but the reaction is controlled so as not to reduce P. (3) is a concept based on a conventional idea, which is a preferable condition in the present invention.

本発明のパウダーを用いることによって、パウダー巻き込みによる表面割れ、疵を防止し、パウダー成分での特有成分に起因するもの疵を低減することができ、図2に示すように、筋状模様発生率を従来の10→0に低減することが出来た。
今回のパウダーの成分、溶鋼の成分を用いた汎用性のある指標化によって、限定された鋼種だけではなく、種々の鋼種においても、同様の効果を得ることができる。
By using the powder of the present invention, surface cracks and scratches due to powder entrainment can be prevented, and scratches caused by peculiar components in the powder component can be reduced. As shown in FIG. 2, the streak pattern occurrence rate can be reduced. Was able to be reduced from the conventional 10 to 0.
By the versatile indexing using the powder component and the molten steel component this time, the same effect can be obtained not only in a limited steel type but also in various steel types.

下記表1の成分の鋼を、表2に記載のパウダーを用いて連続鋳造し、圧延等を経て鋼板のコイルとした。その場合の疵発生有無、および筋状模様発生率を示す。本発明に記載の式の範囲のパウダー成分の場合、疵発生がなく、良好である。 The steels of the components shown in Table 1 below were continuously cast using the powders shown in Table 2 and rolled to obtain steel sheet coils. In that case, the presence or absence of flaws and the occurrence rate of streaky patterns are shown. In the case of the powder component within the range of the formula described in the present invention, there is no defect and it is good.

Claims (1)

Cが質量%で0.0005%以上0.0800%以下の低炭素鋼、極低炭素鋼を連続鋳造する際に使用する連続鋳造用モールドパウダーであって、当該低炭素鋼、極低炭素鋼の成分の鋳片を連続鋳造する際に、鋳型内に供給するモールドパウダーの成分が、下記式(1)を満たすことを特徴とする連続鋳造用モールドパウダー。
([Si]×[P](4/5)×(Al2O3)(4/3))/((SiO2)×(P2O5)(2/5)×[Al](8/3))≧1.64 (1)
ここで、[Si]、[P]、[Al]は溶鋼中の成分の質量%を示し、(Al2O3)、(SiO2)、(P2O5)は、鋳型内の溶融パウダーと溶鋼の界面の部分に分析サンプラーを装入して、サンプリングしたモールドパウダーの溶融物の酸化物成分の質量%である。
Mold powder for continuous casting used for continuous casting of low carbon steel and ultra-low carbon steel in which C is 0.0005% or more and 0.0800% or less in mass%, and the low carbon steel and ultra-low carbon steel. A mold powder for continuous casting, characterized in that the components of the mold powder supplied into the mold during continuous casting of the slabs of the above components satisfy the following formula (1).
([Si] × [P] (4/5) × (Al 2 O 3 ) (4/3) ) / ((SiO 2 ) × (P 2 O 5 ) (2/5) × [Al] (8) / 3) ) ≧ 1.64 (1)
Here, [Si], [P], and [Al] indicate the mass% of the components in the molten steel, and (Al 2 O 3 ), (SiO 2 ), and (P 2 O 5 ) are the molten powders in the mold. The mass% of the oxide component of the melt of the molded powder sampled by charging an analytical sampler at the interface between the and molten steel.
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