JPH08141713A - Mold powder for continuous casting of steel - Google Patents
Mold powder for continuous casting of steelInfo
- Publication number
- JPH08141713A JPH08141713A JP30168694A JP30168694A JPH08141713A JP H08141713 A JPH08141713 A JP H08141713A JP 30168694 A JP30168694 A JP 30168694A JP 30168694 A JP30168694 A JP 30168694A JP H08141713 A JPH08141713 A JP H08141713A
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- powder
- steel
- continuous casting
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Abstract
(57)【要約】
【目的】 本発明は、鋼の連続鋳造用モールドパウダ
ー、特に中炭素鋼用の連続鋳造用モールドパウダーを目
的とする。
【構成】 主成分がCaO、SiO2 で、CaO/Si
O2(wt%塩基度)が1.2〜1.6であって、MgO
含有量が1.5wt%以下である鋼の連続鋳造用パウダ
ーである。(57) [Summary] [Object] The present invention is directed to a mold powder for continuous casting of steel, particularly a mold powder for continuous casting of medium carbon steel. [Structure] Main components are CaO and SiO 2 , CaO / Si
O 2 (wt% basicity) is 1.2 to 1.6, and MgO
It is a powder for continuous casting of steel having a content of 1.5 wt% or less.
Description
【0001】[0001]
【産業上の利用分野】本発明は、鋼、特に中炭素鋼(炭
素含有量0.08〜0.16wt%)の連続鋳造時に鋳
型内の溶鋼に添加される連続鋳造用モールドパウダー
(以下単にパウダーという)に関するものであり、連続
鋳造作業を安定し、鋳片表面の品質が優れた鋳片を連続
鋳造することができるパウダーに関するものである。TECHNICAL FIELD The present invention relates to a continuous casting mold powder (hereinafter simply referred to as a mold powder for continuous casting, which is added to molten steel in a mold during continuous casting of steel, particularly medium carbon steel (carbon content 0.08 to 0.16 wt%). The present invention relates to a powder that stabilizes a continuous casting operation and can continuously cast a slab having excellent slab surface quality.
【0002】[0002]
【従来の技術】鋼の連続鋳造において、パウダーは鋳型
内の溶鋼面に添加され、溶鋼の酸化を防止し、湯面を保
温し、また湯面に浮上してきた介在物を吸収する作用が
ある。また、鋼浴面で溶融したパウダーは鋳型と鋳片間
に流入してフィルム層を形成し、潤滑剤として作用し、
更に抜熱の制御を行なっている。2. Description of the Related Art In continuous casting of steel, powder is added to the molten steel surface in a mold to prevent oxidation of the molten steel, to keep the molten metal surface warm, and to absorb inclusions floating on the molten metal surface. . Further, the powder melted on the steel bath surface flows between the mold and the slab to form a film layer, which acts as a lubricant,
Furthermore, heat removal is controlled.
【0003】従来のパウダーを化学分析すると以下の様
な成分組成になっている。 Si2 O,CaO;20〜40wt%、Al2 O3 ;1〜10wt%、 Na;1〜30wt%、 F;1〜20wt%、 Li;0〜20wt%、 MgO;2〜10wt%、 ZrO2 ;0〜20wt%、 B;0〜10wt% The chemical composition of the conventional powder has the following composition. Si 2 O, CaO; 20~40wt% , Al 2 O 3; 1~10wt%, Na; 1~30wt%, F; 1~20wt%, Li; 0~20wt%, MgO; 2~10wt%, ZrO 2 ; 0 to 20 wt%, B; 0 to 10 wt%
【0004】一方、鋼中炭素濃度が0.08〜0.16
wt%の中炭素領域の鋼(以下、中炭素鋼という)の連
続鋳造において、鋼が液相から固相に変化する際の凝固
収縮率が大きく、そのため鋳片表面に割れ欠陥が発生し
易く、高速鋳造が困難とされてきた。On the other hand, the carbon concentration in steel is 0.08 to 0.16.
In continuous casting of steel in the medium carbon region of wt% (hereinafter referred to as medium carbon steel), the solidification shrinkage rate is large when the steel changes from the liquid phase to the solid phase, so crack defects are likely to occur on the surface of the slab. However, high-speed casting has been difficult.
【0005】これに対し、材料とプロセス−第4巻、第
4号(1991年、1247頁)は、前記中炭素鋼の割
れ欠陥対策として鋳型と鋳片表面間の熱流束低下を低下
させるため、塩基度(wt%CaO/SiO2 )を1.
2以上とし、結晶化時の体積収縮による接触抵抗の増大
をはかり、また、ZrO2 を3.0wt%以上添加する
ことでパウダーフィルムを不透明化し、輻射伝熱の低減
を行ない、清浄な鋳片の製造が可能であることを開示し
ている(従来技術1)。On the other hand, Materials and Processes-Vol. 4, No. 4 (1991, p. 1247) reduce the heat flux between the mold and the surface of the slab as a countermeasure against the crack defects of the medium carbon steel. , Basicity (wt% CaO / SiO 2 ) 1.
2 or more to increase the contact resistance due to volumetric shrinkage during crystallization, and to add ZrO 2 in an amount of 3.0 wt% or more to make the powder film opaque and reduce the radiant heat transfer, and clean slabs It is disclosed that can be manufactured (prior art 1).
【0006】また、品川技報第32号(1989年、1
47頁)は、前記中炭素鋼を鋳造する際、問題となる鋳
片の縦割れを防止するため、モールド内の抜熱速度とパ
ウダーの特性を調査し、溶融したパウダーの凝固過程に
おける結晶化温度を高めることにより、モールド内抜熱
を緩和し、縦割れ発生を減少させ得ることを見出したこ
とを報告している。In addition, Shinagawa Technical Report No. 32 (1989, 1
Page 47) investigates the heat removal rate in the mold and the characteristics of the powder in order to prevent vertical cracking of the slab, which is a problem when casting the medium carbon steel, and crystallizes the molten powder during the solidification process. It has been reported that it was found that by raising the temperature, heat removal in the mold can be relaxed and the occurrence of vertical cracks can be reduced.
【0007】さらに、高塩基度パウダーほど結晶化温度
が高くなる傾向があるとし、また、Na2 O,F,Li
2 O,B2 O3 ,BaO,MgO,Al2 O3 などの成
分が、結晶化温度に影響しているため、パウダーの品質
設定に当たっては、これらの成分組成に留意が必要であ
ることが記載されている(従来技術2)。上記において
結晶化とは溶融したパウダーが鋳型と鋳片表面の間に流
入し、凝固する際に溶融体の一部がガラス相(過冷体)
になるが、他の部分が結晶体として析出する現象であ
る。Further, it is assumed that the higher the basicity powder, the higher the crystallization temperature tends to be, and Na 2 O, F, Li
Since components such as 2 O, B 2 O 3 , BaO, MgO, and Al 2 O 3 influence the crystallization temperature, it is necessary to pay attention to the composition of these components when setting the powder quality. It is described (prior art 2). In the above, crystallization means that melted powder flows between the mold and the surface of the slab, and when it solidifies, part of the melt becomes a glass phase (supercooled body).
However, this is a phenomenon in which other parts are precipitated as crystals.
【0008】[0008]
【発明が解決しようとする課題】従来技術1では、塩基
度を1.2以上に上げることにより、パウダー融体の結
晶化度は大きくなるが、最近指向されている高速鋳造用
パウダーのようにNa,F,Liなどの低融点化促進元
素、低粘性化促進元素が共存すると結晶化度は低下し、
高塩基度化のみの効果では表面欠陥を抑制する結晶化度
は得られない。In the prior art 1, although the crystallinity of the powder melt is increased by increasing the basicity to 1.2 or more, the powder melt has a crystallinity higher than that of the recently-proposed high-speed casting powder. When a low melting point promoting element such as Na, F or Li and a low viscosity promoting element coexist, the crystallinity decreases,
Crystallinity that suppresses surface defects cannot be obtained only by the effect of increasing the basicity.
【0009】更に、従来技術1ではZrO2 による結晶
化促進効果を開示しているが、パウダーにZrO2 を添
加するとパウダーの融点が上昇し、溶鋼表面上のパウダ
ー溶融層が薄くなる他、溶鋼面に浮上する非金属介在物
の吸収能力が低下するため鋳片表面欠陥が発生する問題
がある。Further, in Prior Art 1, the crystallization promoting effect of ZrO 2 is disclosed, but when ZrO 2 is added to the powder, the melting point of the powder rises and the powder molten layer on the surface of the molten steel becomes thin, There is a problem that the slab surface defect occurs because the absorption capacity of non-metallic inclusions floating on the surface decreases.
【0010】また、従来技術2においても高塩基度化が
有効であることを開示しているものの、他のフラックス
成分の結晶化に及ぼす影響については定性的に論じてい
るのみで、有効な結晶化促進元素について定量的には言
及してはいない。Although the prior art 2 also discloses that the high basicity is effective, the effect on the crystallization of other flux components is only qualitatively discussed, and the effective crystal is effective. It does not quantitatively refer to the accelerating elements.
【0011】本発明は、上述した問題を解決し、パウダ
ーに本来の要求される迅速溶融、高潤滑特性を維持しつ
つ、溶融パウダーの高結晶化度を十分に達成することに
よって、鋳片表面の割れ欠陥のない高品位の製品を得る
ことができるパウダーを提供するものである。The present invention solves the above-mentioned problems and sufficiently achieves high crystallinity of the molten powder while maintaining the rapid melting and high lubrication characteristics originally required for the powder, thereby achieving the surface of the slab. The present invention provides a powder capable of obtaining a high-quality product having no crack defects.
【0012】[0012]
【課題を解決するための手段】本発明者等は、各種実験
・検討を重ねた結果、パウダー本来の要求される迅速溶
融、高潤滑特性が維持される範囲において、連続鋳造用
モールドパウダーの主成分であるCaO、SiO2 の塩
基度(wt%)CaO/SiO2 を1.2〜1.6(w
t%比)の範囲でMgOの含有量を1.5wt%以下と
することにより、従来の高塩基度パウダーよりも、パウ
ダー融体の結晶化を促進することができ、これにより、
清浄な表面品質の中炭素鋼の連続鋳造が可能となるとの
知見を得て、以下の発明をするに至った。Means for Solving the Problems As a result of various experiments and studies, the inventors of the present invention have found that in the range where the rapid melting and high lubrication characteristics originally required by the powder are maintained, the mold powder for continuous casting is mainly used. CaO is a component, SiO 2 basicity of (wt%) CaO / SiO 2 1.2~1.6 (w
By setting the content of MgO in the range of (t% ratio) to 1.5 wt% or less, crystallization of the powder melt can be promoted as compared with the conventional high basicity powder.
Based on the finding that continuous casting of medium carbon steel with clean surface quality becomes possible, the inventors have made the following inventions.
【0013】(1)請求項1の発明は、主成分がCa
O、SiO2 で、CaO/SiO2(wt%塩基度)が
1.2〜1.6であって、MgO含有量が1.5wt%
以下である鋼の連続鋳造用パウダーを提供する。 (2)請求項2の発明は、下記の成分組成を有する鋼の
連続鋳造用パウダーを提供する。 (a)MgO含有量が1.5wt%以下、(b)氷晶
石、NaF、蛍石、ソーダ灰、Li2 Oの何れか1種以
上の含有量が4〜25wt%、(c)カーボンブラッ
ク、鱗状黒鉛の何れか1種以上の含有量が1〜8wt
%、(d)残部がCaO、SiO2 で、CaO/SiO
2(wt%塩基度)が1.2〜1.6である。(1) In the invention of claim 1, the main component is Ca.
O, SiO 2 , CaO / SiO 2 (wt% basicity) is 1.2 to 1.6, and MgO content is 1.5 wt%
The following are powders for continuous casting of steel. (2) The invention of claim 2 provides a powder for continuous casting of steel having the following component composition. (A) MgO content is 1.5 wt% or less, (b) Content of at least one of cryolite, NaF, fluorite, soda ash, Li 2 O is 4 to 25 wt%, (c) carbon The content of at least one of black and scaly graphite is 1 to 8 wt.
%, (D) The balance is CaO, SiO 2 , CaO / SiO
2 (wt% basicity) is 1.2 to 1.6.
【0014】[0014]
【作用】一般的に連続鋳造用パウダーが形成する溶融体
は、珪酸塩融体(溶融珪酸塩)であり、種々のイオン、
錯イオンからなるイオン性融体である。スラグ中ではイ
オン性の高いアルカリ金属酸化物、及びアルカリ土類金
属酸化物中の金属は、イオン化傾向が強く、他方、Si
O2 のように共有結合性が高いものは単純にイオン化し
ないで、SiO4 4-,Si2 O7 6-等の錯イオンを形成
する。[Function] Generally, the melt formed by the powder for continuous casting is a silicate melt (molten silicate), and various ions,
It is an ionic melt composed of complex ions. Alkali metal oxides with high ionicity in slag and metals in alkaline earth metal oxides have a strong ionization tendency, while Si
A substance having a high covalent bond such as O 2 does not simply ionize but forms a complex ion such as SiO 4 4− or Si 2 O 7 6− .
【0015】後者はいわゆるガラス形成に大きく寄与す
る網目形成酸化物(Network Former、以下NWFとい
う)であり、前者はCaOに代表されるようにSiO2
の網目構造にOを与え、SiO2 の分子間結合を切断し
て重合度を下げるので修飾酸化物(Network Modifyer、
以下NWMという)として挙動する。この中で、Al2
O3 やFe2 O3 は、一般的にはNWFであるが、酸素
ポテンシャルの高い溶融スラグ中ではNWMとなる。The latter is a network forming oxide (hereinafter referred to as NWF) which greatly contributes to so-called glass formation, and the former is SiO 2 as represented by CaO.
O is added to the network structure of SiO 2 to break the intermolecular bond of SiO 2 and reduce the degree of polymerization.
(Hereinafter referred to as NWM). In this, Al 2
O 3 and Fe 2 O 3 are generally NWF, but become NWM in the molten slag having a high oxygen potential.
【0016】さらに、発明者等が注目したMgOはCa
O/SiO2 系融体中では、若干効果が小さいものの、
NWMとして挙動し結晶化促進元素として評価されてき
た。また、従来MgOはモールドパウダー製造原料の不
純物として、必然的に1.7wt%程度以上パウダー中
に含有されていた。Further, MgO, which the present inventors have noticed, is Ca
In the O / SiO 2 type melt, although the effect is slightly small,
It behaves as an NWM and has been evaluated as a crystallization promoting element. Further, conventionally, MgO was inevitably contained in the powder in an amount of 1.7 wt% or more as an impurity in the raw material for producing mold powder.
【0017】一方、パウダーの結晶化の評価は、溶融パ
ウダーの冷却過程でパウダーの融体から結晶が晶出する
温度を示差熱分析法を用いて結晶化に伴う発熱ピークを
測定することにより行う。この結晶生成温度が高いパウ
ダーほど結晶化が進行しやすい。On the other hand, the crystallization of the powder is evaluated by measuring the temperature at which crystals crystallize from the melt of the powder during the cooling process of the molten powder, by using the differential thermal analysis method to measure the exothermic peak associated with the crystallization. . The higher the crystal formation temperature, the easier the crystallization will proceed.
【0018】発明者等は、パウダーの成分元素の増減に
よる結晶生成温度の制御方法について研究した結果、C
aO/SiO2 が1.2〜1.6の領域においてMgO
が0〜10wt%の範囲(0wt%を含む)ではMgO
成分量が少ないほど結晶生成温度が上昇するという新た
な発見をした。The present inventors have studied the method of controlling the crystal formation temperature by increasing and decreasing the constituent elements of the powder, and as a result, C
MgO in the region of aO / SiO 2 of 1.2 to 1.6
Is in the range of 0 to 10 wt% (including 0 wt%), MgO
I made a new discovery that the crystal formation temperature rises as the amount of components decreases.
【0019】すなわち、パウダー融体中のMgO量を低
減することにより、結晶生成温度が上昇し、その結果、
結晶生成を早めるだけでなく、比較的粘度の低い温度域
での結晶成長も促進され、結晶化をいっそう促進させる
ことができることを見いだした。That is, by reducing the amount of MgO in the powder melt, the crystal formation temperature rises, and as a result,
It has been found that not only the crystal formation is accelerated, but also the crystal growth in a temperature range where the viscosity is relatively low is promoted, and the crystallization can be further promoted.
【0020】さらに、MgOは融点が高く難融物質であ
るため、MgO量を減少させることでモールドパウダー
の溶融性も向上させることになる。すなわち、MgO含
有量の低減は結晶化作用を促進し、溶融性の向上を可能
にする。Furthermore, since MgO has a high melting point and is a refractory substance, reducing the amount of MgO also improves the meltability of the mold powder. That is, the reduction of the MgO content promotes the crystallization effect and enables the meltability to be improved.
【0021】数値限定について 発明者等は、中炭素鋼の良好な鋳造と清浄な鋳片をえる
ためにパウダー融体の結晶化について研究した結果、パ
ウダー融体の結晶生成温度を1130℃以上にすること
により、鋳片の表面欠陥低減効果が大きくなることを知
見した。1300℃における粘性値が0.1Pa・S以
下であるモールドパウダーの場合、以下のような成分組
成を選択する必要がある。 Regarding Numerical Limits The inventors have studied the crystallization of the powder melt in order to obtain good casting of medium carbon steel and clean slab, and as a result, the crystal formation temperature of the powder melt was set to 1130 ° C. or higher. By doing so, it was found that the effect of reducing surface defects of the slab becomes large. In the case of a mold powder having a viscosity value of 0.1 Pa · S or less at 1300 ° C., it is necessary to select the following component composition.
【0022】主成分;本発明のパウダーの主成分はCa
OとSiO2 であり、これらを予め溶融したプリメルト
材を用いる。その配合の割合は塩基度により定めること
ができる。塩基度は1.2未満では、パウダーの融点が
低すぎて望ましくない。他方、塩基度が1.6を超える
とパウダーの融点が高すぎて望ましくない。Main component: The main component of the powder of the present invention is Ca
O and SiO 2 , which are pre-melted materials that are pre-melted are used. The mixing ratio can be determined by the basicity. If the basicity is less than 1.2, the melting point of the powder is too low, which is not desirable. On the other hand, if the basicity exceeds 1.6, the melting point of the powder is too high, which is not desirable.
【0023】MgO;MgOは1.5wt%を超える
と、結晶生成温度が1130℃未満となり、前述の通り
望ましくない。MgO: When MgO exceeds 1.5 wt%, the crystal formation temperature becomes less than 1130 ° C., which is not desirable as described above.
【0024】物性調整剤;氷晶石(人造氷晶石を含
む)、NaF,蛍石、ソーダ灰,Li2O等の粉末を1
種以上の合計が4〜25wt%が望ましい。この範囲よ
り少なくても多くても溶鋼面におけるパウダーの溶解性
が望ましくないからである。Physical property adjusting agent; powder of cryolite (including artificial cryolite), NaF, fluorspar, soda ash, Li 2 O, etc.
It is desirable that the total of four or more species be 4 to 25 wt%. This is because the solubility of the powder on the molten steel surface is undesired if it is less or more than this range.
【0025】溶融速度調整材;カーボンブラックと鱗状
黒鉛が望ましい。溶融速度調整材は溶鋼面に添加された
パウダーの溶融速度を調整する機能がある。カーボンブ
ラックは0.5〜5wt%、鱗状黒鉛は0.5〜3wt
%以下の配合が望ましい。具体的な配合量は鋳造条件に
決定すればよい。より好ましくは、カーボンブラックが
1.2〜2.0wt%、鱗状黒鉛が0.5〜1.5wt
%がよい。Melt rate adjusting material: Carbon black and scaly graphite are preferable. The melting rate adjusting material has a function of adjusting the melting rate of the powder added to the molten steel surface. Carbon black is 0.5-5 wt%, scaly graphite is 0.5-3 wt%
% Or less is desirable. The specific blending amount may be determined by casting conditions. More preferably, carbon black is 1.2 to 2.0 wt% and scaly graphite is 0.5 to 1.5 wt.
% Is good.
【0026】[0026]
【実施例】この発明を実施例により、比較例と対比しな
がら説明する。MgO含有量が極めて少ない珪石、石
灰、蛍石、ガラス粉、アルカリ金属炭酸塩、アルカリ土
類金属炭酸塩と、MgOを実質的に含まないモールドパ
ウダー組成となる工業用試薬とを電気炉において溶融
し、急冷後粉砕し、調整したモールドパウダー主原料を
製造した。EXAMPLES The present invention will be described with reference to examples and comparison with comparative examples. Melt silica stone, lime, fluorite, glass powder, alkali metal carbonate, alkaline earth metal carbonate having extremely low MgO content and an industrial reagent having a mold powder composition substantially free of MgO in an electric furnace Then, it was rapidly cooled and then pulverized to prepare an adjusted mold powder main material.
【0027】この主原料に物性調整剤として人造氷晶
石、NaF,蛍石、ソーダ灰,Li2O等の粉末を1種
以上の合計が4〜25wt%を添加し、更に本発明の範
囲内のMgO成分量にした供試体(以下、発明体とい
う)1〜4を調整した。比較のためにMgO成分量が本
発明の範囲外にあるパウダー供試体(以下、比較体とい
う)1〜6を調整した。表1に発明体1〜4及び比較体
1〜6のMgO量、塩基度(CaO/SiO2 )、結晶
生成温度を示す。To this main raw material, one or more powders of artificial cryolite, NaF, fluorspar, soda ash, Li 2 O and the like are added as a physical property modifier in a total amount of 4 to 25 wt%, and the range of the present invention is further added. Specimens (hereinafter, referred to as invention bodies) 1 to 4 having the amount of MgO component in each of them were adjusted. For comparison, powder samples (hereinafter, referred to as comparative samples) 1 to 6 in which the amount of MgO component was outside the range of the present invention were prepared. Table 1 shows the amounts of MgO, basicity (CaO / SiO 2 ), and crystal formation temperature of Inventions 1-4 and Comparatives 1-6.
【0028】上述した発明体1〜4及び比較体1〜6の
各々を使用し、鋳造速度を1.6m/min、または
1.8m/minとして割れ感受性の大きい中炭素鋼を
連続鋳造したときの、鋼中炭素濃度、モールドパウダー
消費量、鋳片の縦割れ発生指数を調べその結果を表2に
示した。Continuous casting of medium carbon steel having high cracking sensitivity at a casting speed of 1.6 m / min or 1.8 m / min using each of the above inventive bodies 1 to 4 and comparative bodies 1 to 6 The carbon concentration in steel, the amount of mold powder consumed, and the index of vertical crack initiation of slab were examined, and the results are shown in Table 2.
【0029】[0029]
【表1】 [Table 1]
【0030】[0030]
【表2】 [Table 2]
【0031】表1及び表2から明らかなように、MgO
量と塩基度(CaO/SiO2 )が本発明の範囲内にあ
る発明体1〜4は結晶生成温度がいずれも高く1130
℃を超え、前記発明体1〜4を使用した鋳造結果におい
ても縦割れ発生はなく、良好な表面の鋳片を製造でき、
従来困難であった中炭素鋼の高速鋳造を容易に行うこと
ができた。As is clear from Tables 1 and 2, MgO
Inventors 1 to 4 whose amount and basicity (CaO / SiO 2 ) are within the range of the present invention have high crystal formation temperatures of 1130.
C., vertical cracking does not occur even in the casting results using the invention bodies 1 to 4, and a slab having a good surface can be produced,
High-speed casting of medium carbon steel, which was difficult in the past, could be easily performed.
【0032】これに対し、塩基度(CaO/SiO2 )
が本発明の範囲内の1.2〜1.6にあるもののMgO
量が本発明の範囲を超えている比較体1〜6は結晶生成
温度が1125℃以下となり、縦割れ発生指数が高くな
りMgO量が増すにつれてその傾向は著しい。On the other hand, the basicity (CaO / SiO 2 )
Within the scope of the present invention from 1.2 to 1.6
In Comparatives 1 to 6 whose amount exceeds the range of the present invention, the crystal formation temperature is 1125 ° C. or lower, the vertical cracking generation index becomes high, and the tendency becomes remarkable as the amount of MgO increases.
【0033】[0033]
【発明の効果】以上述べたように、この発明によれば溶
融性を阻害しない範囲で結晶化度の大きい連続鋳造用モ
ールドパウダーを得ることができて、割れ感受性の大き
い中炭素鋼においても割れ結果のない品質の優れたもの
を連続鋳造することができる。As described above, according to the present invention, it is possible to obtain a mold powder for continuous casting having a large crystallinity within a range that does not impair the meltability, and to crack even medium carbon steel having a high cracking susceptibility. It is possible to continuously cast a product of excellent quality with no result.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 森 孝志 東京都千代田区丸の内一丁目1番2号 日 本鋼管株式会社内 (72)発明者 近藤 裕計 東京都千代田区丸の内一丁目1番2号 日 本鋼管株式会社内 (72)発明者 西町 龍三 東京都千代田区丸の内一丁目1番2号 日 本鋼管株式会社内 (72)発明者 渡辺 圭児 東京都千代田区丸の内一丁目1番2号 日 本鋼管株式会社内 (72)発明者 宮本 明 東京都千代田区丸の内一丁目1番2号 日 本鋼管株式会社内 (72)発明者 酒井 英典 東京都千代田区丸の内二丁目3番2号 鋼 管鉱業株式会社内 (72)発明者 清水 正明 東京都千代田区丸の内二丁目3番2号 鋼 管鉱業株式会社内 (72)発明者 和泉 洋 東京都千代田区丸の内二丁目3番2号 鋼 管鉱業株式会社内 (72)発明者 川島 健 東京都千代田区丸の内二丁目3番2号 鋼 管鉱業株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Takashi Mori, 1-2 Marunouchi, Chiyoda-ku, Tokyo Nihon Kokan Co., Ltd. (72) Yukei Kondo 1-2-1-2, Marunouchi, Chiyoda-ku, Tokyo Main Steel Pipe Co., Ltd. (72) Inventor Ryuzo Nishimachi Marunouchi 1-2-2, Chiyoda-ku, Tokyo Japan Steel Pipe Co., Ltd. (72) Inventor Keiji Watanabe 1-2, Marunouchi, Chiyoda-ku, Tokyo Japan Steel Pipe Co., Ltd. (72) Inventor Akira Miyamoto 1-2 1-2 Marunouchi, Chiyoda-ku, Tokyo Nihon Steel Pipe Co., Ltd. (72) Inori Hidenori Sakai 2-3-2 Marunouchi, Chiyoda-ku, Tokyo Steel Pipe Mining Co., Ltd. (72) Inventor Masaaki Shimizu 2-3-2 Marunouchi, Chiyoda-ku, Tokyo Steel Pipe Mining Co., Ltd. (72) Inventor Hiroshi Izumi Maru, Chiyoda-ku, Tokyo The inner-chome No. 3 No. 2 steel pipe mining within Co., Ltd. (72) inventor Ken Kawashima, Chiyoda-ku, Tokyo Marunouchi 2-chome No. 3 No. 2 steel pipe Mining Co., Ltd. in
Claims (2)
SiO2(wt%塩基度)が1.2〜1.6であって、M
gO含有量が1.5wt%以下である鋼の連続鋳造用パ
ウダー。1. Main components are CaO and SiO 2 , and CaO /
SiO 2 (wt% basicity) is 1.2 to 1.6, M
Powder for continuous casting of steel having a gO content of 1.5 wt% or less.
パウダー。 (a)MgO含有量が1.5wt%以下、(b)氷晶
石、NaF、蛍石、ソーダ灰、Li2 Oの何れか1種以
上の含有量が4〜25wt%、(c)カーボンブラッ
ク、鱗状黒鉛の何れか1種以上の含有量が1〜8wt
%、(d)残部がCaO、SiO2 で、CaO/SiO
2(wt%塩基度)が1.2〜1.6である。2. A powder for continuous casting of steel having the following composition of components. (A) MgO content is 1.5 wt% or less, (b) Content of at least one of cryolite, NaF, fluorite, soda ash, Li 2 O is 4 to 25 wt%, (c) carbon The content of at least one of black and scaly graphite is 1 to 8 wt.
%, (D) The balance is CaO, SiO 2 , CaO / SiO
2 (wt% basicity) is 1.2 to 1.6.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP06301686A JP3142216B2 (en) | 1994-11-11 | 1994-11-11 | Mold powder for continuous casting of steel |
CN95119219A CN1053131C (en) | 1994-11-11 | 1995-11-10 | Casting powder for steel continuous casting |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP06301686A JP3142216B2 (en) | 1994-11-11 | 1994-11-11 | Mold powder for continuous casting of steel |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH08141713A true JPH08141713A (en) | 1996-06-04 |
JP3142216B2 JP3142216B2 (en) | 2001-03-07 |
Family
ID=17899926
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP06301686A Expired - Fee Related JP3142216B2 (en) | 1994-11-11 | 1994-11-11 | Mold powder for continuous casting of steel |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP3142216B2 (en) |
CN (1) | CN1053131C (en) |
Cited By (7)
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CN102009146A (en) * | 2010-12-08 | 2011-04-13 | 西峡龙成冶金材料有限公司 | Carbon steel continuous casting powder in phi 700-800mm round billet |
JP2011147979A (en) * | 2010-01-22 | 2011-08-04 | Sumitomo Metal Ind Ltd | Mold flux for continuous casting of steel |
CN102615259A (en) * | 2012-04-10 | 2012-08-01 | 河南省西保冶材集团有限公司 | Protective material for non-oriented clean silicon steel continuous casting crystallizer for nuclear power unit |
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KR20170003642A (en) | 2014-06-10 | 2017-01-09 | 신닛테츠스미킨 카부시키카이샤 | MOLD FLUX FOR CONTINUOUS CASTING OF Ti-CONTAINING SUB-PERITECTIC STEEL AND CONTINUOUS CASTING METHOD |
KR20170033389A (en) | 2014-09-11 | 2017-03-24 | 신닛테츠스미킨 카부시키카이샤 | Mold flux for continuous casting of steel |
KR20180079380A (en) | 2015-11-05 | 2018-07-10 | 신닛테츠스미킨 카부시키카이샤 | Continuous Casting Mold Flux and Continuous Casting Method |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1075407C (en) * | 1997-12-12 | 2001-11-28 | 日铁建材工业株式会社 | Steel Continuous Casting Mold Flux |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2530052A1 (en) * | 1975-07-05 | 1977-01-27 | Schaeffler Ohg Industriewerk | COUPLING FOR TOTATABLE CONNECTION OF ASSOCIATED SECTIONS OF A DELIVERY SHAFT FOR TEXTILE MACHINERY |
-
1994
- 1994-11-11 JP JP06301686A patent/JP3142216B2/en not_active Expired - Fee Related
-
1995
- 1995-11-10 CN CN95119219A patent/CN1053131C/en not_active Expired - Lifetime
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JP2011147979A (en) * | 2010-01-22 | 2011-08-04 | Sumitomo Metal Ind Ltd | Mold flux for continuous casting of steel |
CN102009146A (en) * | 2010-12-08 | 2011-04-13 | 西峡龙成冶金材料有限公司 | Carbon steel continuous casting powder in phi 700-800mm round billet |
CN102615259A (en) * | 2012-04-10 | 2012-08-01 | 河南省西保冶材集团有限公司 | Protective material for non-oriented clean silicon steel continuous casting crystallizer for nuclear power unit |
CN102773438A (en) * | 2012-07-25 | 2012-11-14 | 洛阳市科丰冶金新材料(集团)有限公司 | Slag powder of continuous casting and rolling sheet billet low-carbon steel crystallizer |
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Also Published As
Publication number | Publication date |
---|---|
JP3142216B2 (en) | 2001-03-07 |
CN1053131C (en) | 2000-06-07 |
CN1130110A (en) | 1996-09-04 |
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