JPH105953A - Front powder for steel continuous casting - Google Patents
Front powder for steel continuous castingInfo
- Publication number
- JPH105953A JPH105953A JP17546996A JP17546996A JPH105953A JP H105953 A JPH105953 A JP H105953A JP 17546996 A JP17546996 A JP 17546996A JP 17546996 A JP17546996 A JP 17546996A JP H105953 A JPH105953 A JP H105953A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- casting
- continuous casting
- melting
- powder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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- Continuous Casting (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、鋼の連続鋳造の鋳
造初期において、適切な速度で溶融してスラグ層を形成
し溶鋼面を被覆するとともに、潤滑作用を行うスラグフ
ィルムを形成することにより、安定した操業と優れた鋳
片を製造するために使用するフロントパウダーに関する
もので、特に中炭素鋼の連続鋳造において、鋳造初期の
ブレークアウトの防止および鋳片表面の割れに最大の効
果を発揮する。BACKGROUND OF THE INVENTION The present invention relates to a method for forming a slag film which melts at an appropriate speed to form a slag layer to cover a molten steel surface and to form a lubricating action in an early stage of continuous casting of steel. This is related to front powder used for stable operation and producing excellent slabs.Especially for continuous casting of medium carbon steel, it has the greatest effect on preventing breakout at the early stage of casting and cracking on the slab surface. I do.
【0002】[0002]
【従来の技術】近年、鋼の連続鋳造は、省エネルギーや
省資源、歩留りや原単位の向上によるコストダウンのた
め高速化、さらには高速連続鋳造で製造された鋳片を冷
却、再加熱することなく直接圧延工程に送り込む直接圧
延方式が、積極的に採用されるようになっている。この
直接圧延を実施するためには、鋳造される鋳片の欠陥を
極力少なくする必要があり研究がなされているが、中炭
素鋼や包晶組成の鋼では鋳造初期にブレークアウトや割
れが発生しやすく、大きな問題として残っている。2. Description of the Related Art In recent years, continuous casting of steel has been accelerated in order to save energy and resources, to reduce costs by improving yields and unit consumption, and to cool and reheat slabs produced by high-speed continuous casting. The direct rolling method of feeding directly into the rolling process has been actively adopted. In order to perform this direct rolling, it is necessary to minimize defects in the cast slab, and research has been conducted.However, breakouts and cracks occur in the early stage of casting for medium carbon steel and peritectic composition steel. It is easy to do and remains a big problem.
【0003】この割れの発生を防止するためには、鋳片
の冷却を均一にすることが必要であり、そのためにはパ
ウダーの凝固温度を高めて鋳型と鋳片間に流入して形成
されるスラグフィルム自体の伝熱抵抗を大きくすること
により、鋳片から鋳型への伝熱抵抗を大きくして、鋳片
を緩冷却することが有効とされている。しかしながらこ
のようなパウダーを使用しても、鋳造初期においては、
溶鋼の温度低下や溶融スラグ層不足などにより、スラグ
の潤滑性が不足したり不均一流入が起こり、定常操業時
に比較して拘束性ブレークアウトや割れが多く発生す
る。このように本体パウダーの改良だけはこれらの問題
を解決できていない。In order to prevent the occurrence of the cracks, it is necessary to make the cooling of the slab uniform, and for that purpose, the solidification temperature of the powder is raised to flow between the mold and the slab. By increasing the heat transfer resistance of the slag film itself, it is effective to increase the heat transfer resistance from the slab to the mold and slowly cool the slab. However, even if such a powder is used, in the early stage of casting,
Due to a decrease in the temperature of the molten steel or a shortage of the molten slag layer, the lubricity of the slag is insufficient or uneven inflow occurs, and constrained breakouts and cracks occur more frequently than in a normal operation. Thus, improvement of the main body powder alone has not solved these problems.
【0004】これらの問題を解決する目的で鋳造開始時
に使用するフロントパウダーも提案されている。すなわ
ち、鋳造初期の安定した操業を確保する手段として、発
熱パウダーを鋳造初期に使用する方法がとられている。
この鋳造初期に使用するパウダーとしては、例えば特公
昭57−7211号、特公平6−73728号の各公報
に開示されているが、各々パウダー本来の機能を迅速に
発揮させるものおよび、発熱反応後はパウダー本来の役
割を果たす必要があるとの記述が示すように、これらの
フロントパウダーは発熱性を除き、一般パウダー(本体
パウダー)が有する溶融したスラグ特性を特別に変えた
ものではないことがわかる。このように発熱の機能を付
与した上記公告公報の発明では、中炭素鋼の鋳造初期の
拘束性ブレークアウトや割れを十分防止できていないの
が現状である。In order to solve these problems, a front powder used at the start of casting has been proposed. That is, as a means for securing a stable operation in the early stage of casting, a method of using a heat generating powder in the early stage of casting has been adopted.
The powder used in the early stage of the casting is disclosed in, for example, JP-B-57-7211 and JP-B-6-73728, each of which is capable of rapidly exhibiting the original function of the powder, and those having an exothermic reaction. As the description indicates that these powders need to fulfill the role of powder, these front powders do not specially alter the molten slag properties of general powders (body powders), except for heat generation. Recognize. In the invention of the above-mentioned official gazette having the function of generating heat as described above, at present, it is not possible to sufficiently prevent restraint breakout or cracking in the early stage of casting of medium carbon steel.
【0005】[0005]
【発明が解決しようする課題】本発明は、前記従来技術
で解決できなかった鋳造初期におけるブレークアウト
や、鋳片表面の割れを防止するために、鋳造初期に必要
な特有の機能を持つ、鋳造初期に使用するフロントパウ
ダーを提供するものであり、特に中炭素鋼の連続鋳造に
おいて、鋳造初期のブレークアウトの防止および鋳片表
面の割れに最大の効果を発揮する。SUMMARY OF THE INVENTION The present invention relates to a casting method having a specific function required in the early stage of casting in order to prevent breakout in the early stage of casting and cracks in the surface of the slab which could not be solved by the prior art. The present invention provides a front powder to be used at an early stage. Particularly, in continuous casting of medium carbon steel, it exerts a maximum effect on prevention of breakout at an early stage of casting and crack on a slab surface.
【0006】[0006]
【課題を解決するための手段】本発明者らは、中炭素鋼
の連続鋳造初期のブレークアウトや鋳片表面の割れを防
止するための研究を行なった結果、本体パウダーと異な
った特性を有するフロントパウダーを見いだし、鋳造初
期に使用することにより鋳造初期のブレークアウトの防
止および鋳片表面の割れを解決できることを見いだし
た。Means for Solving the Problems The present inventors have conducted research on preventing breakout and cracking of the surface of a slab in the early stage of continuous casting of medium carbon steel. A front powder was found and found to be able to prevent breakout at the beginning of casting and solve cracks on the slab surface by using it at the beginning of casting.
【0007】すなわち、手段1は炭素含有量が0.08
〜0.18重量%の中炭素鋼を連続鋳造で鋳造する際、
凝固温度が1000℃以下、溶融温度が930℃以上、
粘度;1.5〜4.0poise、溶融速度;3.5〜
7.0g/cm2 ・minであるフロントパウダーであ
る。That is, the means 1 has a carbon content of 0.08
When casting medium carbon steel of ~ 0.18 wt% by continuous casting,
Solidification temperature is 1000 ° C or less, melting temperature is 930 ° C or more,
Viscosity; 1.5 to 4.0 poise, melting rate;
The front powder is 7.0 g / cm 2 · min.
【0008】また手段2は、成分組成が酸化物に換算し
て、CaO/SiO2 =0.60〜1.00(重量%
比)の範囲で、Al2 O3 ;3〜7重量%、Na2 O;
0.6〜13重量%、Li2 O;0.5重量%以上、
F;6〜12重量%、Fe2 O3;7〜14重量%不可
避的遊離炭素が1.0重量%以下であり、その成分組成
の内に、酸化剤として酸化鉄を7〜14重量%配合し、
発熱剤としてCa−Si合金を溶融速度が3.5〜7g
/cm2 ・minとなるように配合したフロントパウダ
ーである。Means 2 is that the component composition is expressed as CaO / SiO 2 = 0.60-1.00 (% by weight)
Ratio), Al 2 O 3 ; 3 to 7% by weight, Na 2 O;
0.6 to 13% by weight, Li 2 O; 0.5% by weight or more,
F; 6 to 12 wt%, Fe 2 O 3; 7-14 wt% unavoidable free carbon is 1.0 wt% or less, within its chemical composition, 7-14 wt% iron oxide as an oxidizing agent Mix,
Melting rate of Ca-Si alloy as exothermic agent is 3.5-7 g
/ Cm 2 · min.
【0009】さらに手段3は、手段2においてLi2 O
を5重量%以下としたフロントパウダーである。Further, the means 3 is the same as the means 2 except that Li 2 O
Is 5% by weight or less.
【0010】[0010]
【発明の実施の形態】炭素含有量が0.08〜0.18
重量%の中炭素鋼の連続鋳造において、鋳造初期は溶鋼
温度が低いことや低鋳造速度のため、鋳片の定常時にお
いて最適なパウダー(本体パウダー)では、凝固フィル
ム厚の過剰成長または不均一凝固、流入不足、スラグベ
アの成長などが発生し、これが起因となりブレークアウ
トや鋳片表面の割れが発生することが分かった。DETAILED DESCRIPTION OF THE INVENTION The carbon content is between 0.08 and 0.18.
In the continuous casting of medium-weight carbon steel by weight, due to the low molten steel temperature and the low casting speed in the early stage of casting, the optimum powder (body powder) in the steady state of the slab is overgrown or uneven in the solidified film thickness. It was found that solidification, insufficient inflow, growth of slag bear, etc. occurred, which caused breakout and cracks on the slab surface.
【0011】この凝固フィルムを形成して緩冷却による
均一冷却を図るという一般的な方法は、鋳造初期におい
てはかえって効果がなく、潤滑フィルムを通して鋳型に
よる均一冷却が非常に有効であり、このためフロントパ
ウダーの凝固温度を1000℃以下にする必要がある。The general method of forming a solidified film to achieve uniform cooling by slow cooling is rather ineffective at the beginning of casting, and uniform cooling by a mold through a lubricating film is very effective. The solidification temperature of the powder needs to be 1000 ° C. or less.
【0012】この凝固温度が1000℃より高いと、不
均一な凝固フィルムの形成が進み効果がなくなる。ま
た、このフロントパウダーは、後に使用する本体パウダ
ーよりはるかに低凝固温度であるため、初期の目的を果
たした後、鋳型より流出して高凝固温度の本体パウダー
にスムーズに置換されるので、特性の異なるパウダーを
連続して使用することによる悪影響が見られないことも
特徴の一つである。When the solidification temperature is higher than 1000 ° C., the formation of a non-uniform solidified film proceeds and the effect is lost. In addition, since this front powder has a much lower solidification temperature than the main body powder used later, after fulfilling the initial purpose, it flows out of the mold and is smoothly replaced by the main body powder with a high solidification temperature, One of the characteristics is that no adverse effect is seen by using powders of different types continuously.
【0013】さらに、溶融温度を930℃以上にするの
は、溶融温度がこれより低くなると溶融速度が速くなり
すぎるか、または溶融時にフラックス成分の揮発による
白煙の発生や、スラグの泡立ちが急増し実用的でなくな
るだけでなく、目的とした効果も得られなくなる。Further, the melting temperature is set to 930 ° C. or higher because if the melting temperature is lower than this, the melting rate becomes too high, or the generation of white smoke due to the volatilization of the flux components and the rapid rise of slag foaming during melting. In addition to being practical, the intended effect cannot be obtained.
【0014】粘度は鋳造初期は低速のため、1.5po
ise以下では溶融スラグが流出し、鋳型と鋳片の間に
部分的な空隙ができ不均一冷却となる。4.0pois
e以上では、本体パウダーとの置換がスムーズに行われ
るのを阻害し、割れが発生する。Since the viscosity is low at the beginning of casting, the viscosity is 1.5 po
If the temperature is less than "ise", molten slag flows out, and a partial gap is formed between the mold and the slab, resulting in uneven cooling. 4.0pois
Above e, smooth replacement with the main body powder is hindered, and cracks occur.
【0015】そして、かかる特性のフロントパウダーを
鋳造初期に必要量供給し、かつ最適な溶融状況を得るた
めには、溶融速度を3.5〜7.0g/cm2 ・min
にする必要がある。溶融速度が3.5g/cm2 ・mi
n以下では潤滑に必要な溶融スラグの不足によるブレー
クアウトが発生する。溶融速度が7.0g/cm2 ・m
in以上では一旦半溶融状況になったスラグ表面が冷却
され、塊状または板状に固化し操業トラブルを起こす。In order to supply a required amount of front powder having such characteristics in the early stage of casting and to obtain an optimum melting state, the melting rate is set to 3.5 to 7.0 g / cm 2 · min.
Need to be Melting rate is 3.5 g / cm 2 · mi
Below n, breakout occurs due to lack of molten slag required for lubrication. Melting rate is 7.0 g / cm 2 · m
In the case of in or more, the slag surface once in a semi-molten state is cooled and solidified into a lump or a plate to cause an operation trouble.
【0016】また本発明はさらに効果を高めるために、
安定した溶融速度および溶融状況が得られるフロントパ
ウダーを提示している。すなわち、凝固温度が1000
℃以下で粘度が1.5〜4.0poiseの特性で、フ
ラックス成分の揮発による白煙の発生や泡立ちを抑える
ためには、CaO/SiO2 を0.6〜1.0重量%
比、Al2 O3 を3〜7重量%にすることで可能とな
る。このCaO/SiO2が0.6重量%以下でAl2
O3 が7重量%以上になると粘度を下げるために、Na
2 O、Fなどフラックス成分が過剰となる。CaO/S
iO2 が1.0重量%比以上でAl2 O3 が3重量%以
下では凝固温度を下げ、かつ粘度を範囲内に高く維持す
ることが困難となる。The present invention further enhances the effect by:
The present invention proposes a front powder capable of obtaining a stable melting rate and a stable melting state. That is, when the solidification temperature is 1000
The viscosity is 1.5 to 4.0 poise at a temperature of not more than 0 ° C. In order to suppress generation of white smoke and foaming due to volatilization of a flux component, 0.6 to 1.0% by weight of CaO / SiO 2 is used.
It becomes possible by setting the ratio and Al 2 O 3 to 3 to 7% by weight. When the content of CaO / SiO 2 is 0.6% by weight or less, Al 2
When O 3 is 7% by weight or more, Na is added to decrease the viscosity.
Flux components such as 2 O and F become excessive. CaO / S
When the content of iO 2 is 1.0% by weight or more and the content of Al 2 O 3 is 3% by weight or less, it is difficult to lower the solidification temperature and maintain the viscosity within the range.
【0017】CaO/SiO2 を0.6〜1.0重量%
比で、Al2 O3 を3〜7重量%において、フラックス
成分であるNa2 O、F、Li2 Oにより凝固温度が1
000℃以下、溶融温度を900℃以上、粘度を1.5
〜4.0poiseに調整が可能になる。0.6 to 1.0% by weight of CaO / SiO 2
In terms of the ratio, when the Al 2 O 3 content is 3 to 7% by weight, the solidification temperature is 1 due to the flux components of Na 2 O, F and Li 2 O.
000 ° C or lower, melting temperature 900 ° C or higher, viscosity 1.5
Adjustment to ~ 4.0 poise is possible.
【0018】Na2 Oが7重量%以下では凝固温度また
は粘度を十分下げることができず、Na2 Oが13重量
%以上になると、白煙や泡立ちが急増する。またFが5
重量%以下では粘度が高くなりすぎ、12重量%以上に
なると粘度が低くなり、また白煙や泡立ちを増長させ
る。When the content of Na 2 O is 7% by weight or less, the solidification temperature or viscosity cannot be sufficiently lowered, and when the content of Na 2 O exceeds 13% by weight, white smoke and foaming increase rapidly. F is 5
If it is less than 12% by weight, the viscosity will be too high, and if it is more than 12% by weight, the viscosity will be low, and white smoke and foaming will increase.
【0019】この白煙や泡立ちを抑える成分としてLi
2 Oは非常に有効であると共に、図1、図2に示すよう
に、当該パウダーの凝固温度が低下することを抑制し、
鋳片の表面割れおよびブレークアウトの発生を抑制する
効果がある。しかし、Li2Oが0.5重量%以下では
効果が不足し、5重量%を超えてもその効果は飽和した
状態であり、経済面からみてそれ以上の添加の必要はな
い。As a component for suppressing this white smoke and foaming, Li
2 with O is very effective, as shown in FIGS. 1 and 2, to prevent the solidification temperature of the powder is lowered,
This has the effect of suppressing the occurrence of surface cracks and breakout of the slab. However, if the content of Li 2 O is 0.5% by weight or less, the effect is insufficient, and if the content exceeds 5% by weight, the effect is in a saturated state, and it is not necessary to add further from the viewpoint of economy.
【0020】また、これら成分のフロントパウダーを前
記3.5〜7.0g/cm2 ・minの溶融速度で安定
して溶融させるため、発熱を利用することが有効であ
る。この発熱は不可避的遊離炭素を低減して、Ca−S
i合金と酸化鉄の組み合わせによる酸化還元反応を利用
することが、成分や特性への影響が少なく最適である。
酸化鉄は7重量%以下では溶融速度が遅くなる。14重
量%以上では溶融速度が速すぎるか、白煙の発生を引き
起こす。In order to stably melt the front powder of these components at the melting rate of 3.5 to 7.0 g / cm 2 · min, it is effective to use heat generation. This exotherm reduces unavoidable free carbon, resulting in Ca-S
It is optimal to use the oxidation-reduction reaction of the combination of the i-alloy and iron oxide with little influence on the components and characteristics.
If the content of iron oxide is 7% by weight or less, the melting rate is low. If it exceeds 14% by weight, the melting rate is too high or white smoke is generated.
【0021】Ca−Si合金の配合重量%は溶融速度が
3.5〜7.0g/cm2 ・minとなるように量を決
定する。成分や原料系によりその量は変化するがおよそ
12〜20重量%である。さらに、不可避的遊離炭素が
1.0重量%を超えて多くなると、溶融速度が遅くなり
3.5g/cm2 ・minを確保できなくなる。このよ
うに発熱性を付与することにより、炭酸塩など溶融過程
で吸熱反応を伴う原料を使用しても安定した溶融速度が
得られる。The amount of the Ca-Si alloy is determined so that the melting rate is 3.5 to 7.0 g / cm 2 · min. The amount varies depending on the components and the raw material system, but is about 12 to 20% by weight. Further, if the unavoidable free carbon content exceeds 1.0% by weight, the melting rate becomes low, and 3.5 g / cm 2 · min cannot be secured. By imparting heat in this manner, a stable melting rate can be obtained even when a raw material that undergoes an endothermic reaction in the melting process such as a carbonate is used.
【0022】また、本発明のフロントパウダーは、鋳造
条件の変動に対する追従を考え原料はすべて100me
sh通過重量%が95%以上の粉末の原料を使用してい
る。使用方法、使用量については鋳造初期のみの使用で
あり、溶鋼面が浸漬ノズルの吐出孔を覆った時に添加
し、使用量は溶鋼上部面積当たり溶融スラグに換算して
7〜15mm/cm2 の厚みに相当する量を添加する。
そして一部、溶融が上部表面に達した時に本体パウダー
を添加する。Further, the front powder of the present invention is made of 100 me
The raw material of the powder whose sh-passing weight% is 95% or more is used. The method of use and the amount of use are only used in the early stage of casting, and are added when the molten steel surface covers the discharge holes of the immersion nozzle, and the amount of use is 7 to 15 mm / cm 2 in terms of molten slag per molten steel upper area. Add an amount corresponding to the thickness.
Then, in part, the body powder is added when the melt reaches the upper surface.
【0023】前記溶融速度は、中周波炉で溶解し、15
50℃に保持した10kgの溶鉄上に、1.0g/cm
2 の量のフロントパウダーを投入して溶融するまでの時
間より求めた。凝固温度は、回転円筒法により1300
℃より1℃/minで温度(T)を下げながら粘度
(η)を測定し、1/Tとlogηの直線関係が結晶析
出による見掛けの粘度の急増で変化する点の温度とし
た。溶融温度は、5mmφ×5mmhの円柱状に形成し
た試料を700℃より10℃/minで昇温し、2.5
mmhの半球状になった時の温度とした。The melting rate is set to 15
1.0 g / cm on 10 kg of molten iron maintained at 50 ° C.
It was determined from the time until the amount of the front powder of No. 2 was charged and melted. The solidification temperature was 1300 by the rotating cylinder method.
The viscosity (η) was measured while lowering the temperature (T) at a rate of 1 ° C./min from 1 ° C., and the temperature was determined as the temperature at which the linear relationship between 1 / T and log η changed due to the sudden increase in apparent viscosity due to crystal precipitation. The melting temperature of the sample formed into a 5 mmφ × 5 mmh cylindrical shape was raised from 700 ° C. at a rate of 10 ° C./min.
It was the temperature at which a hemisphere of mmh was formed.
【0024】[0024]
【実施例】以下に本発明によるフロントパウダーの実施
例と比較例を挙げてさらに具体的に説明する。表1に本
発明品および比較品および実機での使用結果を記載す
る。鋳造条件は、鋳型サイズ220〜280×900〜
1800mm、鋳造鋼種は炭素含有量が0.08〜0.
18%の中炭素鋼。ブレークアウトの防止についての評
価は予知検知によりブレークアウトに至らずとも鋳片焼
き付きの跡が認められたチャージを含めて、チャージ比
での発生比率が0.2%以下を○、2%以下を△、2%
を超えるものを×とした。鋳片表面割れの評価について
は、長さ100mm以上の縦割れに対する手入れ率が、
スラブ長さ比で1.0%以下のものを○、3.0%以下
を△、3.0%を超えるものを×とした。The present invention will be described more specifically below with reference to examples and comparative examples of the front powder according to the present invention. Table 1 shows the results of use of the product of the present invention, the comparative product, and the actual machine. Casting conditions are: mold size 220-280 × 900-
1800 mm, the cast steel grade has a carbon content of 0.08-0.
18% medium carbon steel. The evaluation of the prevention of breakout is as follows: Including the charge in which slab burn-in was found even if it did not lead to the breakout by predictive detection, the rate of occurrence in the charge ratio was 0.2% or less. △, 2%
Those that exceeded were evaluated as ×. Regarding the evaluation of slab surface cracks, the care rate for vertical cracks with a length of 100 mm or more,
A sample having a slab length ratio of 1.0% or less was evaluated as ○, a sample having a slab length ratio of 3.0% or less was evaluated as △, and a sample exceeding 3.0% was evaluated as ×.
【0025】[0025]
【表1】 [Table 1]
【0026】表1のA、B、Cは本発明によるもので、
いずれも良好な結果を示した。比較品Dは溶融温度と粘
度が低く、また、Li2 Oを含まずNa2 OとFが本発
明の範囲より多いため、白煙の発生が激しく鋳片表面品
質も悪かった。比較品Eは凝固温度が本発明範囲より小
さく、また、CaO/SiO2 が本発明範囲より多いた
め、本体パウダーとして良好な溶融特性を有している
が、鋳造初期には不均一な凝固フィルムを形成し、ま
た、潤滑性に劣るため、ブレークアウト(予知検知を含
め)が多く、鋳片表面品質も改善されなかった。A, B and C in Table 1 are according to the present invention.
All showed good results. Comparative product D was low in melting temperature and viscosity, and contained no Li 2 O and contained more Na 2 O and F than in the range of the present invention. Therefore, white smoke was generated and the slab surface quality was poor. Comparative product E has good melting characteristics as a main body powder because the solidification temperature is lower than the range of the present invention and CaO / SiO 2 is higher than the range of the present invention, but the non-uniform solidified film in the early stage of casting And, because of poor lubricity, many breakouts (including predictive detection) and no improvement in slab surface quality.
【0027】[0027]
【発明の効果】本発明のフロントパウダーは、従来困難
とされていた中炭素鋼の鋳造初期のブレークアウトの防
止および鋳片表面品質向上を同時に達成でき、歩留りや
省エネルギーだけでなく、安全な操業をもたらすもので
ある。According to the front powder of the present invention, it is possible to simultaneously prevent breakout in the early stage of casting of medium carbon steel and to improve the surface quality of the slab, which have been considered difficult in the past. Is to bring.
【図1】Li2 Oの添加量とパウダーの凝固温度の関係
を示す図FIG. 1 is a diagram showing the relationship between the amount of Li 2 O added and the solidification temperature of powder.
【図2】Li2 の添加量と鋳片の表面割れ発生率および
ブレークアウト発生率との関係を示す図FIG. 2 is a graph showing the relationship between the amount of Li 2 added and the rate of occurrence of surface cracks and breakouts of a slab.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 三隅 秀幸 大分県大分市大字西ノ洲1番地 新日本製 鐵株式会社大分製鐵所内 (72)発明者 谷口 秀久 大分県中津市牛神114−5 ──────────────────────────────────────────────────の Continuing from the front page (72) Inventor Hideyuki Misumi 1 Nishinosu, Oita, Oita, Nippon Steel Corporation Oita Works (72) Inventor Hidehisa Taniguchi 114-5 Ushigami Nakatsu-shi, Oita
Claims (3)
の中炭素鋼を連続鋳造で鋳造するに際し、凝固温度が1
000℃以下、溶融温度が930℃以上、粘度;1.5
〜4.0poise、溶融速度;3.5〜7.0g/c
m2 ・minであることを特徴とする鋼の連続鋳造用フ
ロントパウダー。1. A carbon content of 0.08 to 0.18% by weight
Solidification temperature is 1 when casting medium carbon steel by continuous casting
000 ° C or lower, melting temperature 930 ° C or higher, viscosity: 1.5
~ 4.0 poise, melting rate; 3.5-7.0 g / c
m 2 · min, a front powder for continuous casting of steel.
SiO2 =0.60〜1.00(重量%比)の範囲で、
Al2 O3 ;3〜7重量%、Na2 O;0.6〜13重
量%、Li2 O;0.5重量%以上、F;6〜12重量
%、Fe2 O3 ;7〜14重量%、不可避的遊離炭素が
1.0重量%以下であり、その成分組成の内に、酸化剤
として酸化鉄を7〜14重量%配合し、発熱剤としてC
a−Si合金を溶融速度が3.5〜7g/cm2 ・mi
nとなるように配合したことを特徴とする請求項1に記
載の鋼の連続鋳造用フロントパウダー。2. The composition of the oxide is CaO /
In the range of SiO 2 = 0.60 to 1.00 (weight% ratio),
Al 2 O 3; 3~7 wt%, Na 2 O; 0.6~13 wt%, Li 2 O; 0.5% by weight or more, F; 6 to 12 wt%, Fe 2 O 3; 7~14 % By weight, unavoidable free carbon is 1.0% by weight or less, and in its component composition, 7 to 14% by weight of iron oxide is mixed as an oxidizing agent, and C is used as a heating agent.
The melting rate of the a-Si alloy is 3.5 to 7 g / cm 2 · mi.
2. The front powder for continuous casting of steel according to claim 1, wherein n is added.
0重量%を限度とする鋼の連続鋳造用フロントパウダ
ー。3. The method according to claim 2, wherein the content of Li 2 O is 5.
Front powder for continuous casting of steel up to 0% by weight.
Priority Applications (1)
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JP17546996A JP3238073B2 (en) | 1996-06-17 | 1996-06-17 | Front powder for continuous casting of steel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17546996A JP3238073B2 (en) | 1996-06-17 | 1996-06-17 | Front powder for continuous casting of steel |
Publications (2)
Publication Number | Publication Date |
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JPH105953A true JPH105953A (en) | 1998-01-13 |
JP3238073B2 JP3238073B2 (en) | 2001-12-10 |
Family
ID=15996611
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JP17546996A Expired - Fee Related JP3238073B2 (en) | 1996-06-17 | 1996-06-17 | Front powder for continuous casting of steel |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007210010A (en) * | 2006-02-09 | 2007-08-23 | Sumitomo Metal Ind Ltd | Mold powder for continuously casting steel, and continuous casting method |
JP2012183572A (en) * | 2011-03-07 | 2012-09-27 | Kobe Steel Ltd | Continuous casting method for controlling slag bear and solidification of molten steel surface in initial stage of casting |
JP2017121640A (en) * | 2016-01-06 | 2017-07-13 | 新日鐵住金株式会社 | Front powder design method, front powder manufacturing method, and front powder |
-
1996
- 1996-06-17 JP JP17546996A patent/JP3238073B2/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007210010A (en) * | 2006-02-09 | 2007-08-23 | Sumitomo Metal Ind Ltd | Mold powder for continuously casting steel, and continuous casting method |
JP4687489B2 (en) * | 2006-02-09 | 2011-05-25 | 住友金属工業株式会社 | Steel continuous casting method |
JP2012183572A (en) * | 2011-03-07 | 2012-09-27 | Kobe Steel Ltd | Continuous casting method for controlling slag bear and solidification of molten steel surface in initial stage of casting |
JP2017121640A (en) * | 2016-01-06 | 2017-07-13 | 新日鐵住金株式会社 | Front powder design method, front powder manufacturing method, and front powder |
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Publication number | Publication date |
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JP3238073B2 (en) | 2001-12-10 |
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