JPH07122089B2 - Method for manufacturing slabs for grain-oriented silicon steel - Google Patents
Method for manufacturing slabs for grain-oriented silicon steelInfo
- Publication number
- JPH07122089B2 JPH07122089B2 JP23030391A JP23030391A JPH07122089B2 JP H07122089 B2 JPH07122089 B2 JP H07122089B2 JP 23030391 A JP23030391 A JP 23030391A JP 23030391 A JP23030391 A JP 23030391A JP H07122089 B2 JPH07122089 B2 JP H07122089B2
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- molten steel
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- secondary refining
- blowing
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Description
【0001】[0001]
【産業上の利用分野】この発明は、変圧器の鉄心材料な
どとして有用な方向性けい素鋼板の、その素材となるス
ラブの製造方法に関し、特にAlとNとを主インヒビター
成分として含有するスラブについて、つくろうとする方
向性けい素鋼板の表面性状の有利な改善を、磁気特性の
劣化なくして可能にする製造方法を提案しようとするも
のである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a slab of grain-oriented silicon steel sheet useful as an iron core material of a transformer, and a slab containing Al and N as main inhibitor components. With respect to the above, the present invention intends to propose a manufacturing method which enables advantageous improvement of the surface properties of the grain-oriented silicon steel sheet to be produced without deterioration of magnetic properties.
【0002】[0002]
【従来の技術】方向性けい素鋼板は、磁気特性として、
磁束密度が高いこと及び鉄損が低いことが要求される。
近年、製造技術の進歩により、例えば板厚0.23mmの鋼板
において磁束密度B8 (磁化力800A/mにおける値):1.
92Tのものが得られ、また鉄損特性W17/50(50Hz、1.7
Tの最大磁化の時の値)が0.90 W/kg の如き優れた製品
の工業的規模での生産も可能となっている。かかる優れ
た磁気特性を有する材料は、鉄の磁化容易である〈001
〉方位が鋼板の圧延方向に高度に揃った結晶方位で構
成されるものであり、かような集合組織は、方向性けい
素鋼板の製造工程中、最終仕上げ焼鈍の際にいわゆるゴ
ス方位と称される{110 }〈001 〉方位を有する結晶粒
を優先的に巨大成長させる二次再結晶と呼ばれる現象を
通じて形成される。この{110 }〈001 〉方位の二次再
結晶粒を十分に成長させるための基本的な要件として
は、二時再結晶過程において{110 }〈001 〉方位以外
の好ましくない方位を有する結晶粒の成長を抑制するイ
ンヒビターの存在と、{110 }〈001 〉方位の二次再結
晶粒が十分に発達するのに好適な一次再結晶組織の形成
とが不可欠であることは周知の事実である。2. Description of the Related Art Grained silicon steel sheets have magnetic properties
High magnetic flux density and low iron loss are required.
In recent years, due to the progress of manufacturing technology, for example, in a steel plate having a plate thickness of 0.23 mm, the magnetic flux density B 8 (value at a magnetizing force of 800 A / m): 1.
92T was obtained, and iron loss characteristics W 17/50 (50Hz, 1.7
It is also possible to produce excellent products on an industrial scale such that the value of T at the maximum magnetization) is 0.90 W / kg. Materials with such excellent magnetic properties are easy to magnetize iron <001
〉 Orientation is composed of crystal orientations that are highly aligned with the rolling direction of the steel sheet, and such a texture is called the so-called Goss orientation during the final finish annealing during the manufacturing process of grain-oriented silicon steel sheet. It is formed through a phenomenon called secondary recrystallization in which crystal grains having a {110} <001> orientation are preferentially grown hugely. The basic requirement for sufficiently growing the secondary recrystallized grains having the {110} <001> orientation is that crystal grains having an unfavorable orientation other than the {110} <001> orientation in the two-hour recrystallization process. It is a well-known fact that the existence of an inhibitor that suppresses the growth of Al and the formation of a primary recrystallized structure suitable for sufficiently developing the secondary recrystallized grains in the {110} <001> orientation are essential. .
【0003】ここにインヒビターとしては、一般にMnS,
MnSe,AlN等の微細析出物が利用され、さらにこれらに加
えて特公昭51-13469号公報や特公昭54-32412号公報に開
示された如きSb、Snなどの粒界偏析型の成分を複合添加
してインヒビターの効果を補強することが行われてい
る。ところでこれまで一般にMnS やMnSeを主要インヒビ
ターとするものは、二次再結晶粒径が小さいので鉄損の
低減には有利であったが、近年、レーザー照射法やプラ
ズマジェット法などを用いて、人工的に擬似粒界を導入
することにより磁区微細化が図れるようになって以来、
二次再結晶粒径のサイズが小さいことによる優位性は低
下し、磁束密度が高いことの優位性が高くなった。磁束
密度の高い方向性けい素鋼板を得る方法は古くから知ら
れていて、例えば特公昭46-23820号公報に記載されてい
るように、鋼中にインヒビター成分としてAlN を含有
させる、最終冷延前の焼鈍の冷却を急冷にしてAlN を
析出させる、最終冷延の圧下率を80〜95%と高圧下率
とする、以上の3点の結合により製造できるとされてい
る。As the inhibitor, MnS,
Fine precipitates such as MnSe and AlN are utilized, and in addition to these, grain boundary segregation type components such as Sb and Sn as disclosed in JP-B-51-13469 and JP-B-54-32412 are combined. Addition is performed to reinforce the effect of the inhibitor. By the way, generally, those using MnS or MnSe as the main inhibitor have been advantageous in reducing iron loss because the secondary recrystallized grain size is small, but in recent years, laser irradiation method and plasma jet method have been used. Since it became possible to miniaturize magnetic domains by artificially introducing pseudo grain boundaries,
The advantage due to the small secondary recrystallized grain size decreased, and the advantage due to the high magnetic flux density increased. A method for obtaining a grain-oriented silicon steel sheet having a high magnetic flux density has been known for a long time.For example, as described in Japanese Patent Publication No. Sho 46-23820, final cold rolling is performed by adding AlN as an inhibitor component to the steel. It is said that it can be manufactured by the above three-point bonding, in which the cooling of the previous annealing is rapidly cooled to precipitate AlN, and the final cold rolling reduction rate is set to 80 to 95% and the high pressure reduction rate.
【0004】しかしAlN をインヒビター成分として含有
する鋼板の製造にあっては、表面欠陥、具体的にはブリ
スターが多発するという問題点があった。この表面欠陥
は、製品板厚が減少するに従い、ますます増加する傾向
を呈し、近年のように鋼板の板厚を薄くすることによっ
て鉄損を低減しようとする場合に大きな問題となってい
た。However, in the production of a steel sheet containing AlN as an inhibitor component, there was a problem that surface defects, specifically blisters, frequently occurred. This surface defect tends to increase more and more as the product plate thickness decreases, and has become a big problem when iron loss is reduced by reducing the plate thickness of the steel plate as in recent years.
【0005】この表面欠陥の成因は、鋳造前の溶鋼中に
多量に存在するN(窒素)が、凝固時にガスとして鋼中
に気泡を形成するためと考えられていて、このような表
面欠陥に対して、その防止策がいくつか提案されてい
る。例えば特公昭49-42208号公報には、けい素鋼の最終
製品にブリスターを発生させないためには溶鋼中のHを
3ppm 以下、Nを〔Al(%) ×103 +40〕ppm 以下とする
必要があることが開示されている。すなわちAlを含有す
るけい素鋼では、Nの含有量が高い場合にブリスターの
発生が認められ、それゆえAlの含有量に応じてNの含有
量を制限する必要があることを示している。また特公昭
49-42211号公報には、鋼中のNの含有量として{Al(%)
×103+50}ppm より高いとブリスターが発生するの
で、この値より以下に抑制することが開示されている。The cause of this surface defect is considered to be that N (nitrogen), which is present in a large amount in the molten steel before casting, forms bubbles in the steel as a gas during solidification. On the other hand, some preventive measures have been proposed. For example, in Japanese Examined Patent Publication No. Sho 49-42208, it is necessary to set H in the molten steel to 3 ppm or less and N to [Al (%) × 10 3 +40] ppm or less in order to prevent blisters from being generated in the final product of silicon steel. It is disclosed that there is. That is, in the Al-containing silicon steel, the occurrence of blisters is observed when the N content is high, and therefore it is necessary to limit the N content depending on the Al content. In addition,
49-42211 discloses that the content of N in steel is {Al (%)
If it is higher than × 10 3 +50} ppm, blistering occurs, so it is disclosed that the amount is suppressed below this value.
【0006】かかる観点から、AlN をインヒビターとし
て含有するけい素鋼板の製造においては、特別な加窒処
理を行わず、工業的に通常含有される程度のN含有量に
なる鋼スラブを用いるか、より高いN量を得ようとする
場合には、かかる工業的に通常含有される程度のN含有
量になる鋼スラブを用いて、冷延工程にて窒化焼鈍によ
る加窒処理を施したり(特公昭54-19189号公報参照)、
特開平2-200731 号公報の実施例1〜3に示されるよう
に60ppm 前後のNを含有するブリスターの発生しないス
ラブを素材として用い、最終仕上げ焼鈍中にNを鋼板中
に侵入させ、加窒する方法が採用されている。From such a viewpoint, in the production of a silicon steel sheet containing AlN as an inhibitor, a steel slab having an N content as industrially contained is used without special nitrification treatment, or In order to obtain a higher N content, a steel slab having an N content that is usually contained industrially is used and subjected to a nitriding annealing nitrification treatment in a cold rolling process (special (See Japanese Patent Publication No. 54-19189),
As shown in Examples 1 to 3 of JP-A-2-200731, a blister-free slab containing about 60 ppm N is used as a material, and N is introduced into the steel sheet during the final finish annealing to perform nitrification. Has been adopted.
【0007】しかしながら以上掲げたブリスター抑制策
のように、Nの含有量を抑制する手法や製造工程の途中
で加窒する手法は、AlN の析出量が不足したり、一定し
なくて磁気特性が不安定になりやすい。特にSbを含有す
る鋼組成では、焼鈍工程における加窒が極めて困難であ
る。このためスラブ素材から十分なN含有量を正確に制
御しておくことが必要とされていた。However, as in the above-mentioned blister suppression measures, the technique of suppressing the N content or the technique of nitrifying during the manufacturing process causes insufficient AlN precipitation amount, or the magnetic properties are not constant. Prone to instability. Particularly with a steel composition containing Sb, it is extremely difficult to perform nitrification in the annealing process. Therefore, it has been necessary to accurately control a sufficient N content from the slab material.
【0008】そこでブリスターの発生なしにけい素鋼の
溶鋼のN含有量を増加させる方法としては、窒化カルシ
ウムをインゴット内に前置して鋼塊のN含有量を制御す
る技術が行われていた。Therefore, as a method of increasing the N content of molten steel of silicon steel without the occurrence of blister, a technique of controlling the N content of the steel ingot by placing calcium nitride in front of the ingot has been used. .
【0009】[0009]
【発明が解決しようとする課題】造塊−分塊から連続鋳
造へとスラブ作製のための鋳造技術の変化に従い、連続
鋳造法においても、Alを含有する方向性けい素鋼板用の
スラブ製造のために、溶鋼中に窒化カルシウムを投入し
た後に連続鋳造して鋳込むことが試みられたが、かかる
方法では却ってブリスターが急増することが判明した。
そこで前述したN含有量をAl含有量に応じて規制する技
術が開発されたわけである。In accordance with the change in casting technology for slab production from ingot-casting to continuous casting, even in the continuous casting method, the slab production for grain-oriented silicon steel sheet containing Al is performed. Therefore, it has been attempted to cast calcium nitride into molten steel and then perform continuous casting, but it has been found that the number of blisters increases sharply by such a method.
Therefore, a technique for regulating the N content according to the Al content has been developed.
【0010】発明者らは、窒化カルシウムを投入して連
続鋳造したときに発生するブリスターの増加は、スラブ
表面近傍のCa系介在物が増加し、それを起点としてN2ガ
スの気泡生成が増加することに起因することをつきとめ
た。すなわち溶鋼をインゴットで凝固させた場合は、凝
固するまで長時間がかかるためにCa系の介在物は十分に
鋼の系外に排出されるのに対して、連続鋳造で凝固させ
た場合は、極めて短時間で凝固するためにCa系介在物が
スラブ表面近傍にトラップされ、それゆえこのCa系介在
物を起点としてブリスターが発生するのである。この機
構から、製品板厚が薄くなるに従い、ブリスターの発生
量が増加する現象も理解できる。すなわち熱間圧延及び
冷間圧延の圧下率が増加するに従って鋼板表層下に潜在
していた欠陥が顕在化してくるためと理解される。The inventors have found that the increase in blisters that occurs when calcium nitride is added and continuous casting increases Ca-based inclusions near the slab surface, and from that, the generation of N 2 gas bubbles increases. I found that it was due to doing. That is, when molten steel is solidified with an ingot, Ca-based inclusions are sufficiently discharged out of the steel system because it takes a long time to solidify, whereas when solidified by continuous casting, The Ca-based inclusions are trapped near the surface of the slab because they solidify in an extremely short time, and therefore blisters are generated starting from the Ca-based inclusions. From this mechanism, it is also possible to understand the phenomenon that the amount of blisters generated increases as the product plate thickness decreases. That is, it is understood that the defects that were latent under the surface layer of the steel sheet become more apparent as the reduction rate of hot rolling and cold rolling increases.
【0011】そこで発明者らは、これらの問題点を回避
すべく、真空脱ガス設備における二次精錬にてN2ガスを
吹き込むことにより、溶鋼中のN含有量を高めることを
試みた。しかしながらこの技術を実際に適用した場合、
ブリスターは防止できるが、製品にふくれが多発し、甚
だしい場合には連続鋳造の次工程であるスラブ加熱とい
う、早い時期からスラブ表面にふくれが発生するという
トラブルが起きた。これは、1350〜1460℃といった高温
に加熱する方向性けい素鋼板の製造時に特有に現れる現
象で、例えばこのスラブを1250℃で加熱した場合には、
こうした欠陥は現れないが、磁気特性は、当然劣悪なも
のとなる。In order to avoid these problems, the inventors tried to increase the N content in the molten steel by blowing N 2 gas in the secondary refining in the vacuum degassing equipment. However, when this technology is actually applied,
Blistering can be prevented, but the product often swells, and in extreme cases, slab heating, which is the next step of continuous casting, causes a problem of blistering on the slab surface from an early stage. This is a phenomenon that appears uniquely during the production of grain-oriented silicon steel sheets that are heated to a high temperature of 1350 to 1460 ° C. For example, when this slab is heated at 1250 ° C,
Although such defects do not appear, the magnetic properties are naturally inferior.
【0012】この発明は、高Nを含有するスラブにおい
て、つくろうとする方向性けい素鋼板にブリスターやふ
くれ等の表面欠陥がなく、表面性状が良好でかつ磁気特
性に優れる、方向性けい素用スラブを有利に製造する方
法を提案することを目的とする。The present invention is directed to a slab containing high N, which is used for grain-oriented silicon which has no surface defects such as blisters and blisters on the grain-oriented silicon steel sheet to be produced and has good surface properties and excellent magnetic properties. The aim is to propose a method for advantageously manufacturing slabs.
【0013】[0013]
【課題を解決するための手段】この発明は、方向性けい
素鋼用の溶鋼を、転炉での一次精錬及び取鍋での二次精
錬によりSi:2.5 〜4.5 wt%、Al:0.010 〜0.040 wt
%、N:0.0050〜0.0130wt%を含む成分組成に溶製した
後、連続鋳造機に鋳込んでスラブを製造するにあたり、
前記一次精錬の後期から二次精錬に先立つまでの間に溶
鋼中へN2ガスを吹き込んで加窒処理を行い、かつこの二
次精錬にて、不活性ガスを吹き込んで酸化物系介在物の
除去処理を施すことにより、溶鋼Nの含有量を上記の範
囲に調整することを特徴とする方向性けい素鋼用スラブ
の製造方法である。SUMMARY OF THE INVENTION The present invention provides molten steel for directional silicon steel by primary refining in a converter and secondary refining in a ladle, Si: 2.5-4.5 wt%, Al: 0.010- 0.040 wt
%, N: 0.0050 to 0.0130 wt% After being melted to a component composition, when cast into a continuous casting machine to manufacture a slab,
Performed blown by pressurized nitrogen treatment of N 2 gas into the molten steel until prior to secondary refining in the late of the primary refining, and at the secondary refining, the oxide inclusions by blowing inert gas A method for producing a slab for grain-oriented silicon steel, characterized in that the content of molten steel N is adjusted to the above range by performing a removal treatment.
【0014】ここに転炉からの出鋼後、二次精錬までの
間に取鍋内にてシリコン合金による脱酸を行うことが有
利である。Here, it is advantageous to carry out deoxidation with a silicon alloy in a ladle after tapping from the converter and before secondary refining.
【0015】以下この発明の解明経緯について説明す
る。発明者らは、ふくれの発生した製品を詳細に調査し
たところ、SiO2やAl203 の微細な介在物を確認し、窒化
処理を行っていない他の製品と比較して酸素含有量が10
ppm程度増加しているという結果を得た。かかる微細な
酸化物は、方向性けい素鋼板特有のもので、10ppm 程度
の酸素の増加でも鋼中の存在個数は多数となる。そこで
この酸化物を核としてスラブ加熱においてNが集合し、
N2の気泡として鋼中に発生したものと思われる。The process of clarifying the present invention will be described below. We have When checking products generated bulging details, check the fine inclusions SiO 2 and Al 2 0 3, the oxygen content as compared with other products not subjected to nitriding treatment Ten
The result is that the value is increased by about ppm. Such fine oxides are peculiar to grain-oriented silicon steel sheets, and even if the amount of oxygen increases by about 10 ppm, the number of them present in the steel becomes large. Therefore, N gathers in the slab heating with this oxide as a nucleus,
It seems that N 2 bubbles were generated in the steel.
【0016】そこから発明者らは、かかる酸化物の除去
が、ふくれの防止に重要であることに思い至った。ここ
にけい素鋼の溶鋼中の酸化物は、極めて微細なため、除
去が難しく、二次精錬における溶鋼の十分な攪拌力と攪
拌時間とを必要とする。ところが従来試みられたように
二次精錬の際、単にN2ガスを吹き込んだ場合では、かか
る酸化物系介在物の除去が困難であることが判明した。From this, the inventors have realized that the removal of such oxides is important for preventing blisters. Since the oxide in the molten steel of silicon steel is extremely fine, it is difficult to remove it, and a sufficient stirring force and stirring time of the molten steel in the secondary refining are required. However, it has been found that it is difficult to remove such oxide inclusions when only N 2 gas is blown in during secondary refining as has been attempted conventionally.
【0017】N含有量は、当初から高めていた方が磁気
特性上からも有利なことから、この発明では二次精錬に
先立ち、例えば一次精錬中に、N2ガス吹き込みによる加
窒処理の採用によって、連続鋳造で製造した製品のブリ
スターの発生が効果的に抑制された加窒が行えること、
また二次精錬の際はArを吹き込むことが、製品のふくれ
発生の防止に有効であることを新規に見出したことが端
緒となって、この発明は完成されたものである。Since it is more advantageous in terms of magnetic properties to increase the N content from the beginning, in the present invention, prior to secondary refining, for example, a nitrification treatment by blowing N 2 gas during primary refining is adopted. By this, it is possible to perform nitrification while effectively suppressing the occurrence of blisters in products manufactured by continuous casting.
Further, the present invention has been completed by newly discovering that blowing Ar in the secondary refining is effective in preventing the occurrence of swelling of the product.
【0018】[0018]
【作用】この発明の方向性けい素鋼スラブの好適成分組
成について説明する。Siは、あまりに少ないと電気抵抗
が小さくなって製品の良好な鉄損特性が得られず、一方
多すぎると冷間圧延が困難になるので2.5 〜4.5%の範
囲とする。The preferred component composition of the grain-oriented silicon steel slab of the present invention will be described. If Si is too small, the electric resistance becomes small and good iron loss characteristics of the product cannot be obtained. On the other hand, if it is too large, cold rolling becomes difficult, so the range is 2.5 to 4.5%.
【0019】次にインヒビターについては、製品が高磁
束密度を得るためにはAlN がとりわけ有利であるので、
この発明でも主要インヒビターとしてAlN を用いるもの
とするが、多すぎるとかえって微細析出が困難となるた
め、0.01≦酸可溶Al≦0.04%とし、Nは、0.0050〜0.01
30%の範囲とする。酸可溶Alが0.01%未満の場合や、N
が0.0050%未満の場合は、インヒビターの量が不足して
磁気特性が劣化し、逆に酸可溶Alが0.04%を超える場合
や、Nが0.0130%を超える場合には、析出するAlN が粗
大化して逆にインヒビターとしての機能が劣化し、磁気
特性が劣化する。Next, regarding the inhibitor, since AlN is particularly advantageous for the product to obtain a high magnetic flux density,
In this invention, AlN is used as the main inhibitor, but if it is too much, fine precipitation is rather difficult. Therefore, 0.01 ≦ acid-soluble Al ≦ 0.04%, and N is 0.0050 to 0.01.
The range is 30%. Acid-soluble Al less than 0.01%, N
When the content is less than 0.0050%, the amount of the inhibitor is insufficient and the magnetic properties are deteriorated. On the contrary, when the acid-soluble Al exceeds 0.04% or N exceeds 0.0130%, the precipitated AlN is coarse. And the function as an inhibitor deteriorates, and the magnetic properties deteriorate.
【0020】ここに主要インヒビターとは、これが欠け
ると二次再結晶粒の発現が不能になるものをいい、この
発明では、主要インヒビターに加えて、副次的なインヒ
ビターを併せて用いても良い。例えば、S、Seをインヒ
ビター形成成分として補助的に含有させてもよい。S、
Seは、MnS 又はMnSeとして析出し、インヒビターとして
有効で、このうちMnSeは特に、最終仕上げ板厚が薄くな
っても抑制効果が強いので好ましい。かようなMnS 、Mn
Seを微細析出させるために好適なSやSeの範囲は、単独
及び併用いずれの場合も0.01〜0.04%程度である。The term "primary inhibitor" as used herein means that the secondary recrystallized grains cannot be expressed if it is lacking. In the present invention, a secondary inhibitor may be used in addition to the major inhibitor. . For example, S and Se may be supplementarily contained as an inhibitor-forming component. S,
Se precipitates as MnS 2 or MnSe and is effective as an inhibitor. Of these, MnSe is particularly preferable because it has a strong suppressing effect even when the final finished plate thickness becomes thin. Such MnS, Mn
The range of S and Se suitable for finely depositing Se is about 0.01 to 0.04% in both cases of single and combined use.
【0021】Mnは、ぜい化防止のために有効な成分であ
り、その効果を発揮させるためには、0.05%以上含有さ
せることが好ましい。一方、上限については、S、Seを
インヒビター形成成分として補助的に含有しない場合に
は0.15%程度、含有する場合には0.10%程度とするのが
望ましい。Mn is an effective component for preventing embrittlement, and in order to exert its effect, it is preferably contained in an amount of 0.05% or more. On the other hand, the upper limit is preferably about 0.15% when S and Se are not supplementarily contained as an inhibitor-forming component, and about 0.10% when S or Se is contained.
【0022】またSb、Cu、Cr、Bi、Sn、B、Ge、P等の
インヒビター補強成分も、適宜添加することができ、そ
の範囲については、Sbは0.015 〜0.060 %、Cuは0.03〜
0.30%、Crは0.02〜0.10%、Biは0.005 〜0.020 %、Sn
は0.03〜0.20%、Bは5〜25ppm 、Geは0.005 〜0.060
%、Pは0.010 〜0.090 %とすることが好ましい。上記
成分の下限については、いずれもインヒビター補強成分
としての効果を発揮させるための最小限であり、また上
限については鋼板のぜい化を回避し、加工性を確保する
ための観点からである。Inhibitor-reinforcing components such as Sb, Cu, Cr, Bi, Sn, B, Ge, and P can also be added as appropriate, and the range is 0.015 to 0.060% for Sb and 0.03 to 0.03 for Cu.
0.30%, Cr 0.02-0.10%, Bi 0.005-0.020%, Sn
Is 0.03 to 0.20%, B is 5 to 25 ppm, and Ge is 0.005 to 0.060.
% And P are preferably 0.010 to 0.090%. The lower limits of the above components are all minimums for exhibiting the effect as an inhibitor reinforcing component, and the upper limits are from the viewpoint of avoiding embrittlement of the steel sheet and ensuring workability.
【0023】Cは、熱延組織改善に有効に寄与する成分
であるが、多すぎると脱炭が困難となるので、0.035 〜
0.090 %程度とすることが好ましい。C is a component that effectively contributes to the improvement of the hot rolled structure, but if it is too much, it becomes difficult to decarburize, so 0.035-
It is preferably about 0.090%.
【0024】また熱間ぜい化に起因した表面欠陥防止の
ためにはMoを、0.005 〜0.020 %の範囲で含有させるこ
とが好ましい。Further, in order to prevent surface defects due to hot embrittlement, Mo is preferably contained in the range of 0.005 to 0.020%.
【0025】かかる鋼組成のスラブの製造のために、ま
ず溶銑を転炉で一次精錬する。この際、転炉での一次精
錬の後期から二次精錬までの間で、N2を含有するガスを
用いて溶鋼の加窒処理を施すことがこの発明の第1の技
術的ポイントである。すなわち通常の転炉吹錬では溶鋼
のN含有量が20〜40ppm であるため、所望のN含有量を
得るためには、次工程の二次精錬にてN2のみの吹き込み
を行う必要があり、この発明の第2の技術的ポイントで
ある二次精錬をArガスを吹き込んで行うことが不可能に
なって、ふくれが生じるうれいがあるからである。した
がってこの目的のためには、二次精錬の前で溶鋼中のN
含有量を高め、好ましくは90ppm以上にまで高めておか
なければならない。なお160ppmを超えると、二次精錬で
の脱窒が困難になるので、160ppmまでのN含有量とする
ことが望ましい。In order to produce a slab having such a steel composition, the hot metal is first refined in a converter. At this time, the first technical point of the present invention is to subject the molten steel to nitrification treatment using a gas containing N 2 between the latter stage of the primary refining in the converter and the second refining. That is, since the N content of molten steel is 20 to 40 ppm in normal converter blowing, it is necessary to blow only N 2 in the secondary refining in the next step in order to obtain the desired N content. This is because it is impossible to carry out the second refining, which is the second technical point of the present invention, by blowing Ar gas, and there is a joy that blistering occurs. Therefore, for this purpose, N in molten steel before secondary refining is
The content should be increased, preferably to 90 ppm or higher. If it exceeds 160 ppm, denitrification in secondary refining becomes difficult, so it is desirable to set the N content to 160 ppm.
【0026】転炉での加窒処理は、吹錬の末期でも、吹
錬終了後のリンス処理時でも、いずれでも良いが、吹錬
の初期ではC0ガスのバブリングのためにNの歩留まりが
極端に悪いので採用しない。またN2含有ガス吹き込み
は、転炉以外でも出鋼後の取鍋内で、該ガスを溶鋼中に
吹き込んで行うことも可能である。The nitriding treatment in the converter may be at the end of blowing or at the time of rinsing after the blowing, but at the beginning of blowing, the N yield is extremely high due to bubbling of C0 gas. I don't use it because it's bad. It is also possible to blow the N 2 -containing gas by blowing the gas into the molten steel in a ladle after tapping other than in the converter.
【0027】加窒処理に用いるガスは、純N2ガスでも、
プロパン等とN2との混合ガスでも良く、また吹き込むノ
ズルは、転炉に吹き込む場合、上吹き転炉ではサブラン
スが、また下吹きや上下吹き転炉では底吹きノズルが挙
げられるが、特に底吹きノズルからの吹き込みが加窒促
進上好適である。The gas used for the nitriding treatment may be pure N 2 gas,
A mixed gas of propane or the like and N 2 may also be used.When blowing into the converter, the nozzle to be blown includes a sublance in the upper blowing converter, and a bottom blowing nozzle in the lower blowing and up / down blowing converters. Blowing from a blowing nozzle is suitable for promoting nitrification.
【0028】次いで転炉から出鋼した溶鋼には、二次精
錬すなわち炉外精錬を施す。この二次精錬に先立ち、シ
リコン合金による脱酸処理を行うことが望ましい。これ
は、脱酸処理から鋳込みまでの時間をできるだけ長時間
とり、酸化物系介在物の溶鋼からの分離浮上を図るため
である。Next, the molten steel discharged from the converter is subjected to secondary refining, that is, out-furnace refining. Prior to this secondary refining, it is desirable to perform deoxidation treatment with a silicon alloy. This is because the time from the deoxidizing treatment to the casting is taken as long as possible to separate and float the oxide-based inclusions from the molten steel.
【0029】二次精錬においては、各種合金添加物を投
入して成分組成の調節を行う。この際、不活性ガスを用
いて酸化物系介在物の分離浮上を行って、溶鋼中のN含
有量の調節を行う。不活性ガス吹き込みを行えば脱窒が
行われるからN成分量の調節も可能となる。In the secondary refining, various alloy additives are added to adjust the component composition. At this time, the oxide inclusions are separated and floated by using an inert gas to adjust the N content in the molten steel. Since denitrification is performed by injecting an inert gas, the amount of N component can be adjusted.
【0030】介在物の除去処理及び脱窒の効果は、吹き
込むガス流量や溶鋼温度、さらに攪拌時間、設備の真空
度等によって変化するから、これらの要素を勘案して処
理を行う。Since the effect of removing inclusions and the effect of denitrification vary depending on the flow rate of gas blown in, the temperature of molten steel, the stirring time, the degree of vacuum of equipment, etc., the treatment is carried out in consideration of these factors.
【0031】不活性ガスとしては、Arが代表として掲げ
られるがこの他、He、Ne、CO等を用いても良いことはい
うまでもない。As the inert gas, Ar is mentioned as a representative, but needless to say, He, Ne, CO or the like may be used.
【0032】二次精錬の設備としては、真空又は減圧、
あるいは減圧加圧の繰り返しで、かつ溶鋼攪拌力として
ガス、雰囲気圧力、電磁力等を使用する、いわゆる真空
また減圧取鍋精錬用設備が適していて、例えばRH,D
H,PM(pulse mixing),VOD,TD,TN,LF,
VAD,VC,VODC,ASEA−SKF等が該当す
る。なかでも真空脱ガス設備が、効率的な介在物除去及
び脱窒として好適である。Equipment for secondary refining includes vacuum or reduced pressure,
Alternatively, a so-called vacuum or reduced pressure ladle refining equipment that repeats depressurization and pressurization and uses gas, atmospheric pressure, electromagnetic force, etc. as a molten steel stirring force is suitable.
H, PM (pulse mixing), VOD, TD, TN, LF,
VAD, VC, VODC, ASEA-SKF, etc. correspond. Among them, the vacuum degassing equipment is suitable for efficient inclusion removal and denitrification.
【0033】かかる工程を経て溶製された溶鋼は、連続
鋳造機によってスラブとされる。連続鋳造の際には公知
の技術を適用すればよい。その後、かかるスラブは必要
により再圧し、サイズを合わせた後、加熱して熱間圧延
を行う。熱間圧延後の鋼帯は、1回の冷間圧延、あるい
は中間焼鈍を挟む2回以上の冷間圧延によって最終板厚
とする。The molten steel melted through the above steps is made into a slab by a continuous casting machine. A known technique may be applied during continuous casting. After that, the slab is repressed if necessary, and the size is adjusted, followed by heating and hot rolling. The steel strip after hot rolling is made into a final strip thickness by one cold rolling or two or more cold rollings with intermediate annealing.
【0034】最終冷延前の焼鈍は、AlN の溶体化のため
には850 〜1200℃の高温が必要であり、また焼鈍後、Al
N の析出のため500 ℃までの急冷処理が必要である。次
に最終冷延の圧下率については、公知のように高磁束密
度を得るためには高圧下率とする必要があり、したがっ
て1回法の圧下率及び2回法における最終冷延の圧下率
はいずれも80〜95%の範囲とする。というのは、圧下率
が80%より少ないと高磁束密度が得られず、一方95%を
超えると2次再結晶が困難となるからである。The annealing before final cold rolling requires a high temperature of 850 to 1200 ° C. for solution treatment of AlN, and after annealing, after annealing
A quenching process up to 500 ° C is required for N precipitation. As for the final cold rolling reduction rate, it is necessary to use a high pressure reduction rate in order to obtain a high magnetic flux density as known in the art. Therefore, the single reduction rolling reduction and the final cold rolling reduction reduction in the two-pass rolling method are performed. Is in the range of 80 to 95%. This is because if the rolling reduction is less than 80%, a high magnetic flux density cannot be obtained, while if it exceeds 95%, secondary recrystallization becomes difficult.
【0035】また冷延工程における焼鈍時の表面の酸化
によって失われる鋼中Nの補給を行う意味で、焼鈍前に
窒化促進剤を塗布して過剰の脱窒を防止することは、得
られる製品の磁気特性の安定のうえで好ましい。Further, in order to replenish the N in the steel which is lost by the oxidation of the surface during annealing in the cold rolling process, it is necessary to apply a nitriding accelerator before annealing to prevent excessive denitrification. Is preferable in terms of stability of magnetic properties.
【0036】なお最終冷延の途中で時効処理を行うこと
は、製品の鉄損を低減するうえで有利である。特にSbを
含有する成分系では、短時間のただ一回の時効処理によ
って磁束密度の格段の向上が認められる点に優れた特徴
がある。最終圧延後の鋼板は脱脂処理を施した後、脱炭
・一次再結晶焼鈍に供される。The aging treatment performed during the final cold rolling is advantageous in reducing the iron loss of the product. In particular, the component system containing Sb has an excellent feature in that the magnetic flux density can be remarkably improved by only one aging treatment for a short time. The steel sheet after the final rolling is subjected to degreasing treatment, and then subjected to decarburization and primary recrystallization annealing.
【0037】次いでMgO を主成分とする焼鈍分離剤を塗
布してから、コイル状に巻かれて最終仕上げ焼鈍に供さ
れ、その後必要に応じて絶縁コーティングを施される
が、時にレーザーやプラズマ、その他の手法によって磁
区細分化処理を施すことも可能であることはいうまでも
ない。Next, an annealing separating agent containing MgO as a main component is applied, and then wound in a coil shape and subjected to final finishing annealing, and then an insulating coating is applied if necessary. It goes without saying that the magnetic domain subdivision processing can be performed by other methods.
【0038】[0038]
【実施例】実施例1 底吹き転炉を用いて吹錬を行い、この際、吹錬終了前3
分間に底吹きノズルを用いてN2ガスを流量150 Nl/ 分で
吹き込んだ。この時、溶鋼のN含有量は123ppmであっ
た。その後、FeSi合金を前置きしてある取鍋中に200 t
出鋼注入し、RH設備でAr吹き込み処理を100 Nl/ 分で
35分間の行った。また各種合金添加物をRH処理中に投
入して表1のA〜Nで示される各種の溶鋼を溶製した。[Example] Example 1 Blowing was carried out using a bottom blowing converter, at this time, before completion of blowing 3
N 2 gas was blown in at a flow rate of 150 Nl / min using a bottom blowing nozzle for 1 minute. At this time, the N content of the molten steel was 123 ppm. After that, place 200 t in the ladle where FeSi alloy was placed in front.
Injecting tapped steel, Ar blowing treatment at RH equipment at 100 Nl / min
I went for 35 minutes. Further, various alloy additives were put into the RH treatment to melt various molten steels shown by A to N in Table 1.
【0039】[0039]
【表1】 [Table 1]
【0040】これらの溶鋼を連続鋳造により厚み250 mm
のスラブとし、再圧処理によって厚み220 mmにした後、
このスラブを1430℃に加熱して厚み2.0 mmまで熱間圧延
を施した。かくして得られた熱延コイルを、1000℃での
熱延板焼鈍の後、厚み1.50mmまで冷間圧延し、1100℃で
の中間焼鈍と引き続く急冷処理の後、再び冷間圧延を施
して厚み0.75mmにし、次いで連続焼鈍炉で300 ℃、1分
間の熱処理を施し、さらに冷間圧延を施して厚み0.23mm
の最終板厚とした。次いで脱脂処理を施したのち、脱炭
・一次再結晶焼鈍を850 ℃、2 分間施し、MgO を主成分
とする焼鈍分離剤を塗布してからコイル状に巻いて1200
℃、10時間の最終仕上げ焼鈍に供し、その後張力付与絶
縁コーティングを施した。かくして得られた製品につい
て、磁気特性と、表面欠陥率を調べた。なお表面欠陥率
は光学的表面欠陥連続測定機で測定した。得られた結果
を表2に示す。These molten steels were continuously cast to a thickness of 250 mm.
Slab and after re-pressing to a thickness of 220 mm,
This slab was heated to 1430 ° C and hot-rolled to a thickness of 2.0 mm. The hot-rolled coil thus obtained was annealed at 1000 ° C., then cold-rolled to a thickness of 1.50 mm, intermediate-annealed at 1100 ° C. and a subsequent quenching treatment, and then cold-rolled again to obtain a thickness. 0.75 mm, then heat treated in a continuous annealing furnace at 300 ° C for 1 minute, then cold rolled to a thickness of 0.23 mm.
And the final plate thickness. Then, after degreasing treatment, decarburization / primary recrystallization annealing is performed at 850 ° C for 2 minutes, an annealing separating agent containing MgO as a main component is applied, and then the material is coiled and wound 1200
It was subjected to final finishing annealing at ℃ for 10 hours, and then applied with a tension-imparting insulating coating. The magnetic properties and surface defect rate of the product thus obtained were examined. The surface defect rate was measured by an optical surface defect continuous measuring machine. The obtained results are shown in Table 2.
【0041】 [0041]
【0042】実施例2 下記の3種類の方法で一次精錬及び二次精錬にて溶製
し、出鋼した。 上下吹き転炉を用いて吹錬した後、底吹きノズルによ
りN2を該転炉内の溶鋼中に吹き込んで1分間リンスを行
った。その後FeSi合金を前置してある取鍋中に出鋼注入
した。この時の溶鋼中のN含有量は108ppmであった。そ
の後RH設備で二次精錬を、Arガスを流量80 Nl/分で40
分間吹き込んで行った。二次精錬後のN含有量は86 pp
mであった(実施例)。 上下吹き転炉を用いて通常の吹錬を行った後、FeSi合
金とCaN2を前置きしてある取鍋中に出鋼注入した。この
時の溶鋼中のN含有量は106ppmであった。次にRH設備
でArを流量150Nl/分で40分間吹き込み、二次洗練を終了
した。この時の溶鋼のN含有量は88ppmであった(比較
例)。 上下吹き転炉を用いて通常の吹錬を行った後、底吹き
ノズルによりN2を該転炉内の溶鋼中に吹き込んで1分間
リンスを行った。その後FeSi合金を前置きしてある取鍋
中に出鋼注入した。この時の溶鋼中のN含有量は82 ppm
であった。次にRH設備でN2を流量80Nl/ 分で40分間吹
き込み二次精錬を終了した。この時の溶鋼のN含有量は
94ppmであった(比較例)。 ,,いずれも二次精錬の間にSi、Mn、Cの含有量
を調整し、Se、Sb、Alを投入して、二次精錬終了時で溶
鋼成分としてC:0.068 〜0.070 %、Si:3.30〜3.32
%、Mn:0.068 〜0.070 %、Al:0.027 〜0.030 %、
S:0.003 %、Se:0.019 〜0.022 %、Sb:0.022 〜0.
026 %、P:0.004 %、残部実質的にFeの組成を得た。
これらの溶鋼は連続鋳造以降、実施例1と同一の処理で
製品にした。かくして得られた製品の磁気特性及び表面
欠陥率を表3に示す。Example 2 Steels were melted by primary refining and secondary refining by the following three types of methods, and tapped. After the blasting was performed using a vertical blowing converter, N 2 was blown into the molten steel in the converter by a bottom blowing nozzle to perform rinsing for 1 minute. After that, the FeSi alloy was poured into the ladle in which the FeSi alloy was placed in advance. The N content in the molten steel at this time was 108 ppm. After that, secondary refining is performed in the RH equipment, and Ar gas is flown at 40 Nl / min.
It was blown in for a minute. N content after secondary refining is 86 pp
m (Example). After performing normal blowing using a vertical blowing converter, steel was poured into a ladle in which FeSi alloy and CaN 2 were placed in advance. The N content in the molten steel at this time was 106 ppm. Then, Ar was blown in the RH facility at a flow rate of 150 Nl / min for 40 minutes to complete the secondary refinement. The N content of the molten steel at this time was 88 ppm (comparative example). After performing normal blowing using a vertical blowing converter, N 2 was blown into the molten steel in the converter by a bottom blowing nozzle to perform rinsing for 1 minute. After that, FeSi alloy was poured into the ladle which was placed in front. The N content in the molten steel at this time is 82 ppm.
Met. Next, N 2 was blown into the RH facility at a flow rate of 80 Nl / min for 40 minutes to complete the secondary refining. The N content of the molten steel at this time is
It was 94 ppm (comparative example).・ ・ ・ In all cases, the contents of Si, Mn, and C are adjusted during secondary refining, Se, Sb, and Al are added, and at the end of secondary refining, C: 0.068 to 0.070%, Si: 3.30 to 3.32
%, Mn: 0.068 to 0.070%, Al: 0.027 to 0.030%,
S: 0.003%, Se: 0.019 to 0.022%, Sb: 0.022 to 0.
A composition of 026%, P: 0.004% and the balance of Fe was obtained.
These molten steels were made into products by the same treatment as in Example 1 after continuous casting. The magnetic properties and surface defect rate of the product thus obtained are shown in Table 3.
【0043】 [0043]
【0044】実施例3 下記の条件で一次精錬及び二次精錬を施した。 上下吹き転炉を用いて吹錬した後、底吹きノズルによ
りN2ガスを該転炉内の溶鋼中に流量190Nl/分で吹き込ん
で1分間リンスを行った。この時の溶鋼中のN含有量は
93 ppmであった。その後FeSi合金を前置きしてある取鍋
中に出鋼注入し、その後RH設備で二次精錬を行う際、
Arガスを流量 40 Nl/ 分で30分間吹き込んで二次精錬を
終了した。終了時の溶鋼中のN含有量は85 ppmであった
(条件I)。 条件と同一条件で転炉中の溶鋼にN2ガスを吹き込ん
だ後、FeSi合金を前置きしてある取鍋中に出鋼注入し
た。この時のN含有量は102 ppm であった。その後RH
設備で二次精錬を行う際、Arを流量80 Nl/分で30分間吹
き込んで二次精錬を終了した。終了時の溶鋼中のN含有
量は90 ppmであった(条件II)。 条件と同一条件で転炉中の溶鋼にN2ガスを吹き込ん
だ後、FeSi合金を前置きしてある取鍋中に出鋼注入し
た。この時のN含有量は99ppmであった。その後、PM
設備で二次精錬を行う際、Arを 70Nl/ 分で30分間吹き
込んで二次精錬を終了した。この時の溶鋼中のN含有量
は89 ppmであった(条件III )。 条件と同一条件で転炉中の溶鋼にN2ガスを吹き込ん
だ後、出鋼時の出鋼流にFeSi合金を添加した。この時の
N含有量は105ppmであった。その後RH設備で条件Iと
同じ条件で二次精錬を行った。終了時の溶鋼中のN含有
量は97 ppmであった(条件IV)。 条件と同一条件で転炉中の溶鋼にN2ガスを吹き込ん
だ後、出鋼した。この時の溶鋼中のN含有量は98ppm で
あった。その後RH設備での二次精錬の初期にFeSi合金
を投入して脱酸処理及びSi含有量の調整を行った。二次
精錬のガスの吹き込みは条件Iと同様に行った。二次精
錬終了時の溶鋼中のN含有量は90 ppmであった(条件
V)。 上下吹き転炉を用いて吹錬した後、FeSiを前置きして
ある取鍋中に出鋼注入した。この時の溶鋼のN含有量は
25ppm であった。次にフラッシング設備を用いて溶鋼中
にN2ガスを吹き込んで加窒処理を行い、溶鋼中のN含有
量を113ppmまで高めた。その後RH設備で二次精錬を行
う際、Arガスを流量100Nl/分で30分間吹き込んで二次精
錬を終了した。この場合、二次精錬後の溶鋼中のN含有
量は90 ppmであった(条件VI)。 上下吹き転炉を用いて吹錬した後、FeSi合金を前置き
してある取鍋中に出鋼注入した。この時の溶鋼中のN含
有量は35ppm であった。次にRH設備で二次精錬を行う
際、Arガスを流量 60 Nl/ 分で30分間吹き込んで二次精
錬を終了し、比較例とした。終了時の溶鋼中のN含有量
は32 ppmであった(条件VII )。Example 3 Primary refining and secondary refining were performed under the following conditions. After blowing using a vertical blowing converter, N 2 gas was blown into the molten steel in the converter at a flow rate of 190 Nl / min by a bottom blowing nozzle to perform rinsing for 1 minute. The N content in the molten steel at this time is
It was 93 ppm. After that, when the FeSi alloy is poured into the ladle that has been placed in front, and then secondary refining is performed in the RH equipment,
The secondary refining was completed by blowing Ar gas at a flow rate of 40 Nl / min for 30 minutes. The N content in the molten steel at the end was 85 ppm (condition I). N 2 gas was blown into the molten steel in the converter under the same conditions, and then the FeSi alloy was poured into the ladle that was placed in front. At this time, the N content was 102 ppm. Then RH
When the secondary refining was performed in the facility, Ar was blown at a flow rate of 80 Nl / min for 30 minutes to complete the secondary refining. The N content in the molten steel at the end was 90 ppm (condition II). N 2 gas was blown into the molten steel in the converter under the same conditions, and then the FeSi alloy was poured into the ladle that was placed in front. At this time, the N content was 99 ppm. Then PM
When carrying out the secondary refining in the facility, Ar was blown at 70 Nl / min for 30 minutes to complete the secondary refining. The N content in the molten steel at this time was 89 ppm (condition III). After N 2 gas was blown into the molten steel in the converter under the same conditions, FeSi alloy was added to the tapping flow at tapping. At this time, the N content was 105 ppm. After that, secondary refining was performed in the RH facility under the same conditions as Condition I. The N content in the molten steel at the end was 97 ppm (condition IV). Under the same conditions, N 2 gas was blown into the molten steel in the converter, and then the steel was tapped. At this time, the N content in the molten steel was 98 ppm. After that, the FeSi alloy was added at the initial stage of the secondary refining in the RH facility to perform deoxidation treatment and adjustment of the Si content. The gas for secondary refining was blown in the same manner as in Condition I. The N content in the molten steel at the end of secondary refining was 90 ppm (condition V). After blowing using a vertical blowing converter, FeSi was poured into a ladle in which FeSi was placed in advance. The N content of the molten steel at this time is
It was 25 ppm. Next, N 2 gas was blown into the molten steel using a flushing equipment to perform a nitrification treatment, and the N content in the molten steel was increased to 113 ppm. After that, when performing secondary refining in the RH facility, Ar gas was blown thereinto at a flow rate of 100 Nl / min for 30 minutes to complete the secondary refining. In this case, the N content in the molten steel after the secondary refining was 90 ppm (condition VI). After blowing using a vertical blowing converter, FeSi alloy was poured into a ladle that had been placed in front. The N content in the molten steel at this time was 35 ppm. Next, when performing secondary refining in the RH facility, Ar gas was blown thereinto at a flow rate of 60 Nl / min for 30 minutes to complete the secondary refining, which was used as a comparative example. The N content in the molten steel at the end was 32 ppm (condition VII).
【0045】条件I〜VII はいずれも二次精錬の間にS
i、Mn及びCの含有量を調整し、Se、Sb、Alを投入し
て、二次精錬終了時に溶鋼成分としてC:0.067 〜0.07
1 %、Si:3.31〜3.33%、Mn:0.070 〜0.073 %、Al:
0.025 〜0.029 %、S:0.003 〜0.005 %、Se:0.020
〜0.022 %、Sb:0.025 〜0.027 %、P:0.002 〜0.00
4%、残部実質的にFeの組成を得た。さらに条件I〜VII
の溶鋼は連続鋳造以降、実施例1と同一の処理で製品
とした。また条件VII の溶鋼は実施例1とほぼ同一の処
理で製品としたが、中間焼鈍及び脱炭焼鈍で加窒を施
し、鋼中N含有量として95ppm まで高めた。これらの製
品の磁気特性及び表面欠陥率を表4に示す。Conditions I to VII are all S during the secondary refining.
After adjusting the contents of i, Mn and C, adding Se, Sb and Al, C: 0.067 to 0.07 as a molten steel component at the end of secondary refining.
1%, Si: 3.31 to 3.33%, Mn: 0.070 to 0.073%, Al:
0.025 to 0.029%, S: 0.003 to 0.005%, Se: 0.020
Up to 0.022%, Sb: 0.025 to 0.027%, P: 0.002 to 0.00
A composition of 4% with the balance being substantially Fe was obtained. Further conditions I to VII
After the continuous casting, the molten steel of No. 2 was manufactured by the same treatment as in Example 1. Further, the molten steel under the condition VII was made into a product by almost the same treatment as in Example 1, but was subjected to nitrification by intermediate annealing and decarburization annealing to increase the N content in the steel to 95 ppm. Table 4 shows the magnetic properties and surface defect rates of these products.
【0046】 [0046]
【0047】[0047]
【発明の効果】この発明の方向性けい素鋼用スラブの製
造方法は、一次精錬の後期から二次精錬に先立つまでの
間に溶鋼中へN2ガスを吹き込んで加窒処理を行い、かつ
この二次精錬にて、不活性ガスを吹き込んで酸化物系介
在物の除去処理を施して溶鋼Nの含有量を上記の範囲に
調整することにより、連続鋳造で製造した製品のブリス
ターの発生を効果的に抑制した上で、加窒処理を製品の
ふくれ発生なく行うことができる。EFFECT OF THE INVENTION The method for producing a slab for directional silicon steel of the present invention is to perform a nitrification treatment by blowing N 2 gas into molten steel between the latter stage of primary refining and prior to secondary refining, and In this secondary refining, an inert gas is blown in to remove oxide inclusions to adjust the content of the molten steel N within the above range, thereby preventing the occurrence of blister in the product manufactured by continuous casting. After effectively suppressing, the nitrification treatment can be performed without the product swelling.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 菅 孝宏 千葉県千葉市川崎町1番地 川崎製鉄株式 会社 技術研究本部内 (72)発明者 飯田 嘉明 岡山県倉敷市水島川崎通一丁目(番地な し) 川崎製鉄株式会社 水島製鉄所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Takahiro Suga 1 Kawasaki-cho, Chiba-shi, Chiba Inside the Technical Research Division, Kawasaki Steel Co., Ltd. ) Kawasaki Steel Co., Ltd. Mizushima Steel Works
Claims (2)
次精錬及び取鍋での二次精錬によりSi:2.5 〜4.5 wt
%、Al:0.010 〜0.040 wt%、N:0.0050〜0.0130wt%
を含む成分組成に溶製した後、連続鋳造機に鋳込んでス
ラブを製造するにあたり、 前記一次精錬の後期から二次精錬に先立つまでの間に溶
鋼中へN2ガスを吹き込んで加窒処理を行い、かつこの二
次精錬にて、不活性ガスを吹き込んで酸化物系介在物の
除去処理を施すことにより、溶鋼Nの含有量を上記の範
囲に調整することを特徴とする方向性けい素鋼用スラブ
の製造方法。1. Si: 2.5 to 4.5 wt% of molten steel for grain-oriented silicon steel is subjected to primary refining in a converter and secondary refining in a ladle.
%, Al: 0.010 to 0.040 wt%, N: 0.0050 to 0.0130 wt%
After melting the component composition comprising, in manufacturing a slab cast in a continuous casting machine, blowing in pressurized nitrogen treatment of N 2 gas into the molten steel during the late of the primary refining until prior to the secondary refining And in the secondary refining, the content of the molten steel N is adjusted to the above range by blowing an inert gas to remove oxide inclusions. Manufacturing method of slab for raw steel.
取鍋内にてシリコン合金による脱酸を行う請求項1記載
の方向性けい素鋼用スラブの製造方法。2. The method for producing a slab for grain-oriented silicon steel according to claim 1, wherein deoxidation with a silicon alloy is carried out in a ladle after tapping from the converter and before secondary refining.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23030391A JPH07122089B2 (en) | 1991-09-10 | 1991-09-10 | Method for manufacturing slabs for grain-oriented silicon steel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23030391A JPH07122089B2 (en) | 1991-09-10 | 1991-09-10 | Method for manufacturing slabs for grain-oriented silicon steel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0565524A JPH0565524A (en) | 1993-03-19 |
| JPH07122089B2 true JPH07122089B2 (en) | 1995-12-25 |
Family
ID=16905721
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP23030391A Expired - Lifetime JPH07122089B2 (en) | 1991-09-10 | 1991-09-10 | Method for manufacturing slabs for grain-oriented silicon steel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07122089B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5810506B2 (en) * | 2010-11-05 | 2015-11-11 | Jfeスチール株式会社 | Oriented electrical steel sheet |
| CN115896602B (en) * | 2022-11-11 | 2024-06-07 | 湖南华菱涟源钢铁有限公司 | Production method of oriented silicon steel plate blank and oriented silicon steel plate blank |
| CN118531288B (en) * | 2024-07-25 | 2024-10-15 | 湖南华菱涟源钢铁有限公司 | Preparation method of oriented silicon steel based on stable nitrogen increase and oriented silicon steel |
-
1991
- 1991-09-10 JP JP23030391A patent/JPH07122089B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0565524A (en) | 1993-03-19 |
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