JPH05360A - Immersion nozzle for continuous casting - Google Patents
Immersion nozzle for continuous castingInfo
- Publication number
- JPH05360A JPH05360A JP3178731A JP17873191A JPH05360A JP H05360 A JPH05360 A JP H05360A JP 3178731 A JP3178731 A JP 3178731A JP 17873191 A JP17873191 A JP 17873191A JP H05360 A JPH05360 A JP H05360A
- Authority
- JP
- Japan
- Prior art keywords
- alumina
- continuous casting
- weight
- graphite
- immersion nozzle
- 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
Landscapes
- Casting Support Devices, Ladles, And Melt Control Thereby (AREA)
- Compositions Of Oxide Ceramics (AREA)
Abstract
(57)【要約】
[目的] ステンレス鋼の鋳造に対して長時間安定的に
鋳造できる連続鋳造用浸漬ノズルを提供する。
[構成] 主成分として黒鉛15〜35重量%、最大粒
径が1mm以下のβ型アルミナ20〜60重量%そして
最大粒径が74μm以下のα型アルミナ25〜65重量
%で構成され、黒鉛の灰分及びβ型アルミナ、α型アル
ミナ中に含まれる不可避的な不純物としてのガラス系成
分を除いてSi,SiC,SiO2を別途添加しないこ
とを特徴とする。
[効果] 特にステンレス鋼を鋳造する際、ノズル内孔
部での地金等の浸潤及び溶損を防止でき、長時間安定的
に使用できる。(57) [Summary] [Object] To provide a continuous casting immersion nozzle capable of stably casting stainless steel for a long time. [Constitution] The main component is composed of 15 to 35% by weight of graphite, 20 to 60% by weight of β-alumina having a maximum particle size of 1 mm or less, and 25 to 65% by weight of α-alumina of maximum particle size of 74 μm or less. It is characterized in that Si, SiC, and SiO 2 are not separately added, except for glass components as unavoidable impurities contained in ash and β-type alumina and α-type alumina. [Effect] Especially when casting stainless steel, it is possible to prevent infiltration and melting damage of the metal in the nozzle inner hole portion, and it can be used stably for a long time.
Description
【0001】[0001]
【産業上の利用分野】この発明は鋼の連続鋳造用浸漬ノ
ズルに関し、特にステンレス鋼を鋳造する際、ノズル内
孔部の地金等の侵潤及び溶損を防止し、安定的に長時間
鋳造できる連続鋳造用浸漬ノズルに関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a dipping nozzle for continuous casting of steel, and particularly when casting stainless steel, prevents invasion and melting damage of the metal in the nozzle inner hole and ensures stable and long-term operation. The present invention relates to a continuous casting immersion nozzle that can be cast.
【0002】[0002]
【従来の技術】タンディシュからモールドに溶鋼を注入
するのに利用される連続鋳造用耐火物として、一般的に
Al2O3―SiO2―黒鉛系耐火物を使用しているが、
特にステンレス鋼は比較的鋼中の酸素レベルが高いた
め、耐火物中のSiO2量に律速されてノズル内孔部へ
の地金の侵潤及び溶損が進行し、短時間の使用しかでき
ない。そのことよりステンレス鋼の鋳造には、耐火物中
のSiO2成分を除去した、Al2O3―SiC―黒鉛系
耐火物が使用されつつある。しかしながら、長時間(例
えば500min以上)鋳造する場合では、耐火物中の
SiCの酸化反応、そしてその後生じる還元反応の進行
により前述と同様、ノズル内孔部への地金の侵潤及び溶
損が進行してしまうため、結局長時間に亘って安定的な
鋳造ができないものとなっている。As a refractory for continuous casting used to inject molten steel from a tundish into a mold, Al 2 O 3 --SiO 2 --graphite refractory is generally used.
In particular, since stainless steel has a relatively high oxygen level in the steel, the rate of SiO 2 in the refractory material limits the rate of infiltration and melting of the metal in the nozzle bore, and it can only be used for a short time. . For this reason, Al 2 O 3 —SiC—graphite refractory from which SiO 2 component in the refractory is removed is being used for casting of stainless steel. However, in the case of casting for a long time (for example, 500 min or more), the infiltration and melting loss of the metal into the nozzle inner hole portion may occur due to the progress of the oxidation reaction of SiC in the refractory and the subsequent reduction reaction, as described above. Since it progresses, stable casting cannot be achieved over a long period of time.
【0003】[0003]
【発明が解決しようとする課題】比較的鋼中の酸素レベ
ルが高く、そして粘性が低いステンレス鋼の連続鋳造に
関して、従来技術の一つであるAl2O3―SiO2―黒
鉛系耐火物では、温度低下の激しいノズル内孔稼働部に
於いて鋼中酸素の析出に伴うFeO,MnO等の生成さ
れた金属酸化物が耐火物中のSiO2と選択的に反応し
溶融,流失し溶損が進行してしまう。またSiO2は高
温下の還元雰囲気に於いてかなり不安定であるため、耐
火物中のCとの還元反応によりガス化し、組織が脆化す
る。またノズル内孔稼働部で生成されるFeO、MnO
及びCr2O3等が耐火物中のCにより還元され、Cの消
費が進み、さらに組織の脆化が進展してしまう。上述の
反応の繰り返しにより順次地金の侵潤,溶損が発生して
いき最終的には異状溶損または脱落等のトラブルに至っ
てしまい、200min程度しか耐用出来なかった。With regard to continuous casting of stainless steel having a relatively high oxygen level and a low viscosity in the steel, Al 2 O 3 --SiO 2 --graphite refractory, which is one of the prior arts, is used. In the working part of the nozzle hole where the temperature drops drastically, the metal oxides generated such as FeO, MnO, etc. accompanying the precipitation of oxygen in the steel selectively react with SiO 2 in the refractory material to melt, flow away and melt damage. Will progress. Further, since SiO 2 is considerably unstable in a reducing atmosphere at a high temperature, it is gasified by the reduction reaction with C in the refractory and the structure becomes brittle. In addition, FeO and MnO produced in the working part of the nozzle inner hole
And Cr 2 O 3 and the like are reduced by C in the refractory, the consumption of C progresses, and the embrittlement of the structure further progresses. By repeating the above-mentioned reaction, infiltration and melting loss of the metal were sequentially generated, and finally a trouble such as abnormal melting loss or falling out was reached, and it was possible to withstand only about 200 minutes.
【0004】そこでさらに耐用延長を計る為に、SiO
2を別途添加しないAl2O3―SiC―黒鉛系耐火物を
使用し対策する場合がある。確かに500min程度ま
で寿命を安定的に延ばすことはできるが、500min
以上の使用に対しては安定的に使用できず、特に静圧の
かかる吐出孔廻りに於いて地金の侵潤が発生し易い。侵
潤層の熱間強度はほとんど無い為最悪の場合、吐出孔落
下に至ってしまう。Therefore, in order to further extend the service life, SiO
In some cases, Al 2 O 3 —SiC—graphite refractory without adding 2 may be used as a countermeasure. It is possible to extend the life stably up to about 500 min, but 500 min
It cannot be used stably for the above-mentioned use, and infiltration of the metal is likely to occur especially around the discharge hole where static pressure is applied. Since there is almost no hot strength in the infiltrated layer, in the worst case, the ejection holes fall.
【0005】これは結局、耐火物中のSiCに起因する
ものと考えられ、時間的要因によりSiCが酸化される
ことで上述と同様、最終的に地金の侵潤層ができてしま
い、長時間鋳造に対して安定性に欠けるものである。After all, this is considered to be caused by SiC in the refractory, and the oxidation of SiC due to a time factor causes the formation of an infiltrated layer of the bare metal in the same manner as described above. It lacks stability in time casting.
【0006】次に他の特性について述べる。低膨張性の
原料であるSiO2が含有されていないAl2O3―黒鉛
系耐火物の場合、Al2O3原料としてα型Al2O3のみ
を使用すると、α型アルミナの高熱膨張特性に起因する
熱的スポーリング特性が大巾に低下してしまう傾向にあ
る。Next, other characteristics will be described. Low expansion Al 2 SiO 2 is not contained as a raw material of the O 3 - For the graphite-based refractory, using only α-type for Al 2 O 3 Al 2 O 3 raw material, the high thermal expansion properties of the α-type alumina The thermal spalling characteristics due to the above tend to be greatly deteriorated.
【0007】そこで、本発明の目的は、ステンレス鋼の
鋳造に対して500min以上の長時間に亘って使用し
てもノズル内孔部に地金の侵潤層を発生させることな
く、また突発的な熱的スポーリングを引き起こすことな
く、安定的に鋳造することができる連続鋳造用ノズルを
提供するものである。Therefore, an object of the present invention is to prevent sudden occurrence of a metal infiltration layer in the nozzle inner hole portion even when it is used for casting stainless steel for a long time of 500 min or more, and it is sudden. Provided is a continuous casting nozzle capable of stable casting without causing a large thermal spalling.
【0008】[0008]
【課題を解決するための手段】この発明は上記の問題点
を解決するためになされたものであって、連続鋳造用浸
漬ノズルで図1の浸漬ノズル1のスラグラインに相当す
る部位B以外で使用する。即ち、図1のA部に主成分と
して、黒鉛15〜35重量%,最大粒径が1mm以下の
β型アルミナ20〜60重量%そして最大粒径が74μ
m以下のα型アルミナ、25〜65重量%で構成され、
黒鉛の灰分,及びβ型アルミナ,α型アルミナ中に含ま
れる不可避的な不純物としてのガラス系成分を除いて、
Si,SiC,SiO2を別途添加しないことを特徴と
するアルミナ−黒鉛系耐火物を配設した連続鋳造用浸漬
ノズルである。The present invention has been made in order to solve the above-mentioned problems, and it is an immersion nozzle for continuous casting other than a portion B corresponding to the slag line of the immersion nozzle 1 of FIG. use. That is, as a main component in part A of FIG. 1, graphite is 15 to 35% by weight, β-alumina having a maximum particle size of 1 mm or less is 20 to 60% by weight, and the maximum particle size is 74 μ.
α-alumina of m or less, composed of 25 to 65% by weight,
Except for the ash content of graphite and the glass-based components as unavoidable impurities contained in β-type alumina and α-type alumina,
This is a continuous casting immersion nozzle in which an alumina-graphite refractory is arranged, in which Si, SiC, and SiO 2 are not added separately.
【0009】[0009]
【作用】この発明によれば、ステレンス鋼の連続鋳造用
浸漬ノズルでアルミナ−黒鉛系耐火物の主成分として、
黒鉛の含有量は15〜35重量%であることが望まし
い。これは含有量が15重量%未満の場合では熱伝導率
の低下、並びに熱膨張率の増大により耐熱スポーリング
特性の劣化を招き、また含有量が35重量%を越えると
耐酸化性並びに耐蝕性が大巾に低下してしまうことにな
る。According to the present invention, as the main component of the alumina-graphite refractory in the immersion nozzle for continuous casting of stainless steel,
The graphite content is preferably 15 to 35% by weight. When the content is less than 15% by weight, the thermal conductivity is lowered and the thermal expansion coefficient is increased, so that the heat resistant spalling property is deteriorated, and when the content exceeds 35% by weight, the oxidation resistance and the corrosion resistance are deteriorated. Will be drastically reduced.
【0010】またβ型アルミナの含有量は20〜60重
量%が望ましい。β型アルミナは化学成分的には11A
l2O3・R2O(R=Na,K)で表され、その結晶構
造は、α型アルミナと同様六方晶系ではあるが、結晶の
格子定数は異なり、結晶軸に対して垂直な方向に顕著な
劈用性を有しており、粒子は弾性を有する平板上である
ため、α型アルミナより耐熱スポーリング性を高めるこ
とができるが、60重量%を越えると結晶中のR2O
(R=Na,K)成分の影響により黒鉛の酸化を促進さ
せ、かつ高温かつ還元雰囲気下に長時間暴露されるとR
2O(R=Na,K)成分の気化によりβ型アルミナが
崩壊してしまい耐蝕性が低下してしまう。また20重量
%未満であると耐熱スポーリング特性を高位に維持する
ことができなくなる。The content of β-alumina is preferably 20 to 60% by weight. β-alumina has a chemical composition of 11A
It is represented by l 2 O 3 · R 2 O (R = Na, K), and its crystal structure is a hexagonal system like α-type alumina, but the lattice constant of the crystal is different and it is perpendicular to the crystal axis. Since it has a remarkable easiness of use in the direction and the particles are on a flat plate having elasticity, the heat-resistant spalling property can be improved more than that of α-alumina, but when it exceeds 60% by weight, R 2 in the crystal is increased. O
The oxidation of graphite is promoted by the influence of (R = Na, K) component, and R is exposed when exposed to high temperature and reducing atmosphere for a long time.
Due to the vaporization of the 2 O (R = Na, K) component, β-type alumina collapses and corrosion resistance decreases. If it is less than 20% by weight, the heat-resistant spalling property cannot be maintained at a high level.
【0011】β型アルミナの粒度は最大粒径として1m
m以下が適当であり、それ以上であると他原料との混合
性が悪くなり、物理特性値のばらつきを引き起こすとと
もに、強度が低値を示してしまう。α型アルミナの含有
量は25〜65重量%が望ましい。即ち、含有量が25
重量%未満であると耐蝕性の低下を招き、また65重量
%を越えると耐熱スポーリング特性が大巾に低下してし
まうことによる。α型アルミナの粒度は最大粒径として
74μm以下が適当であり、それより大きくなると耐蝕
性の向上が期待できず、また強度が低値を示してしま
う。The particle size of β-type alumina is 1 m as the maximum particle size.
A value of m or less is suitable, and if it is more than m, the mixing property with other raw materials deteriorates, causing variations in physical property values, and showing a low strength. The content of α-alumina is preferably 25 to 65% by weight. That is, the content is 25
If it is less than wt%, the corrosion resistance will be deteriorated, and if it exceeds 65 wt%, the heat-resistant spalling property will be greatly deteriorated. The maximum particle size of α-alumina is appropriately 74 μm or less, and if it is larger than that, the corrosion resistance cannot be expected to be improved and the strength will be low.
【0012】次に本発明の連続鋳造用浸漬ノズルを図面
を参照しながら説明する。Next, the continuous casting immersion nozzle of the present invention will be described with reference to the drawings.
【0013】図1は本発明の連続鋳造用浸漬ノズルの概
略垂直断面を示している。本発明の化学成分組成を有す
る耐火物を図1の浸漬ノズル1のA部に配設することに
より、ステンレス鋼を鋳造する際、長時間に亘って溶鋼
と接触するノズル内孔より地金が侵潤することなく、安
定的に使用できるものである。FIG. 1 shows a schematic vertical section of a continuous casting immersion nozzle according to the present invention. By arranging the refractory material having the chemical composition of the present invention in the portion A of the immersion nozzle 1 of FIG. 1, when casting stainless steel, the metal ingot will come out from the nozzle inner hole that is in contact with molten steel for a long time. It can be used stably without infiltration.
【0014】[0014]
【発明の効果】次に実施例を挙げ、この発明の効果を述
べる。The effects of the present invention will be described below with reference to examples.
【0015】[0015]
【実施例】表1に示す本発明の範囲内の化学成分組成を
有する配合物1〜6(以下“本発明のサンプル”とい
う)及び本発明の範囲外の化学成分組成を有する配合物
7〜9(以下“比較サンプル”という)の各々に5〜1
0重量%の範囲内の粉末及び溶液のフェノール樹脂を添
加し、それらを混合及び混練して得られた原料坏土によ
って、酸素濃度を100ppmMn濃度を1.0〜1.
5%,溶鋼温度1550℃に調整した溶鋼に対する耐蝕
性を試験するための30mm×30mm×230mmの
寸法を有する成形体および耐スポーリング性を試験する
ための外径150mm、内径60mmおよび全長400
mmの寸法を有する成形体を作製し各々を1000℃〜
1200℃の範囲内の温度で還元焼成して耐火物1〜1
1を作製した。EXAMPLES Formulations 1 to 6 (hereinafter referred to as “samples of the invention”) having chemical composition within the scope of the present invention shown in Table 1 and formulations 7 to having chemical composition outside the scope of the present invention 5 to 1 for each of 9 (hereinafter referred to as "comparative sample")
Oxygen concentration was 100 ppm and Mn concentration was 1.0-1.Mn based on the raw material kneaded material obtained by adding powder and solution phenol resin in the range of 0 wt% and mixing and kneading them.
5%, molded body having dimensions of 30 mm × 30 mm × 230 mm for testing corrosion resistance to molten steel adjusted to 1550 ° C. and outer diameter 150 mm, inner diameter 60 mm and total length 400 for testing spalling resistance
A molded body having a size of mm is produced and each of
Refractory 1 to 1 by reduction firing at a temperature in the range of 1200 ° C
1 was produced.
【0016】上述した本発明のサンプル1〜6および比
較サンプル7〜11の各々の物理持性値を表1に示す。Table 1 shows the physical endurance values of the above-mentioned samples 1 to 6 of the present invention and comparative samples 7 to 11.
【0017】ついで上述した30mm×30mm×23
0mmの寸法を有する本発明のサンプル1〜6および比
較用サンプル7〜11のそれぞれを酸素濃度が100p
pm,Mn濃度が1.0〜1.5%に調整した1550
℃の温度の溶鋼中に180分間浸漬して溶損率を調査
し、その結果を表1に示す。Next, the above-mentioned 30 mm × 30 mm × 23
Each of Samples 1 to 6 of the present invention and Comparative Samples 7 to 11 having a dimension of 0 mm had an oxygen concentration of 100 p.
1550 with pm and Mn concentrations adjusted to 1.0 to 1.5%
The melting loss rate was investigated by immersing in molten steel at a temperature of ° C for 180 minutes, and the results are shown in Table 1.
【0018】ついで上述した外径150mm、内径60
mm及び全長400mmの寸法を有する本発明のサンプ
ル1〜6及び比較サンプル7〜11のそれぞれを155
0℃の溶鋼中に10分間浸漬させた後、外表面より水に
て急冷させ、亀裂の有無を確認し、耐スポーリング性を
調査し、その結果を表1に示す。Then, the above-mentioned outer diameter 150 mm and inner diameter 60
155 for each of Samples 1-6 of the present invention and Comparative Samples 7-11 having dimensions of mm and total length of 400 mm.
After being immersed in molten steel at 0 ° C. for 10 minutes, it was quenched from the outer surface with water, the presence or absence of cracks was confirmed, and the spalling resistance was investigated. The results are shown in Table 1.
【0019】表1からも明らかなように本発明のサンプ
ルは耐スポーリング性及び耐蝕性に優れているが、一方
比較用のサンプルでは例えばサンプル7に於いては黒鉛
の含有量が少なく、かつα型アルミナの含有量が高い事
に起因して耐スポーリング性が著しく劣る結果となっ
た。また、比較サンプル8に於いては黒鉛の含有量が高
い事に起因して耐蝕性が著しく劣り、更には比較サンプ
ル9に於いてはα型アルミナの含有量が低い事に起因し
て比較サンプル10及11に於いては化学成分値では、
本発明のサンプル2と同じではあるが、β型及α型アル
ミナの粒度が粗い事に起因して強度が低値を示しかつ溶
損率も劣化してしまう結果となった。As is clear from Table 1, the sample of the present invention has excellent spalling resistance and corrosion resistance, while the comparative sample, for example, sample 7, has a low graphite content, and The result was that the spalling resistance was significantly inferior due to the high content of α-alumina. Further, in Comparative Sample 8, the corrosion resistance is remarkably poor due to the high graphite content, and in Comparative Sample 9, the comparative sample 9 is low in the α-alumina content. In 10 and 11, the chemical composition value is
Although it is the same as the sample 2 of the present invention, the strength was low and the melt loss rate was deteriorated due to the coarse particle size of β-type and α-type alumina.
【0020】以上の結果を踏まえて表1に示す本発明の
サンプル2に於いて、図1に示す連続鋳造用用浸漬ノズ
ルを作製し、取鍋70tonステンレス鋼(JIS規
格:SUS304)のスラブ連鋳機にセットし実機によ
り900min鋳造したところノズル内孔部での地金の
侵潤は全く認められず長時間安定的に使用出来ることを
立証した。On the basis of the above results, in the sample 2 of the present invention shown in Table 1, the immersion nozzle for continuous casting shown in FIG. 1 was prepared, and a ladle 70 ton stainless steel (JIS standard: SUS304) slab series was prepared. When it was set in a casting machine and cast for 900 minutes with an actual machine, no infiltration of the metal in the nozzle inner hole was observed and it was proved that it could be used stably for a long time.
【0021】この結果より本発明の化学成分組成を有す
るアルミナ―黒鉛系耐火物を用いた浸漬ノズルではステ
ンレス鋼を長時間に亘って鋳造することを可能とするも
のである。From these results, the immersion nozzle using the alumina-graphite refractory having the chemical composition of the present invention makes it possible to cast stainless steel for a long time.
【図1】本発明の連続鋳造用浸漬ノズルの説明縦断面図
である。FIG. 1 is an explanatory longitudinal sectional view of a continuous casting immersion nozzle of the present invention.
1 浸漬ノズル A 部 B 部位 1 immersion nozzle Part A B part
Claims (3)
ルに於いて、主成分として黒鉛15〜35重量%,β型
アルミナ20〜60重量%,α型アルミナ25〜65重
量%を含有していることを特徴とする連続鋳造用浸漬ノ
ズル。1. A dipping nozzle for continuous casting of alumina-graphite, containing 15 to 35% by weight of graphite, 20 to 60% by weight of β-type alumina, and 25 to 65% by weight of α-type alumina as main components. Immersion nozzle for continuous casting characterized by
分,β型アルミナ及α型アルミナ中の不可避的な不純物
としてのガラス系成分を除いてSi,SiC,SiO2
を別途添加しないことを特徴とする請求項1記載の連続
鋳造用浸漬ノズル。2. Alumina-graphite refractory contains Si, SiC, SiO 2 except for graphite ash and glass-based components as unavoidable impurities in β-type alumina and α-type alumina.
2. The immersion nozzle for continuous casting according to claim 1, wherein is not added separately.
してα型アルミナの最大粒径は74μm以下とする請求
項1記載の連続鋳造用浸漬ノズル。3. The continuous casting immersion nozzle according to claim 1, wherein the maximum particle size of β-alumina is 1 mm or less and the maximum particle size of α-alumina is 74 μm or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3178731A JPH0747196B2 (en) | 1991-06-24 | 1991-06-24 | Immersion nozzle for continuous casting |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3178731A JPH0747196B2 (en) | 1991-06-24 | 1991-06-24 | Immersion nozzle for continuous casting |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05360A true JPH05360A (en) | 1993-01-08 |
| JPH0747196B2 JPH0747196B2 (en) | 1995-05-24 |
Family
ID=16053597
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3178731A Expired - Lifetime JPH0747196B2 (en) | 1991-06-24 | 1991-06-24 | Immersion nozzle for continuous casting |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0747196B2 (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59146976A (en) * | 1983-02-10 | 1984-08-23 | 明智セラミツクス株式会社 | Steeping nozzle for continuous casting |
-
1991
- 1991-06-24 JP JP3178731A patent/JPH0747196B2/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59146976A (en) * | 1983-02-10 | 1984-08-23 | 明智セラミツクス株式会社 | Steeping nozzle for continuous casting |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0747196B2 (en) | 1995-05-24 |
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