AU730801B2 - A continuous casting nozzle for casting molten steel - Google Patents

A continuous casting nozzle for casting molten steel Download PDF

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Publication number
AU730801B2
AU730801B2 AU45229/97A AU4522997A AU730801B2 AU 730801 B2 AU730801 B2 AU 730801B2 AU 45229/97 A AU45229/97 A AU 45229/97A AU 4522997 A AU4522997 A AU 4522997A AU 730801 B2 AU730801 B2 AU 730801B2
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Australia
Prior art keywords
continuous casting
roseki
nozzle
alumina
molten steel
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Ceased
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AU45229/97A
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AU4522997A (en
Inventor
Toshiyuki Muroi
Shojiro Naito
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Akechi Ceramics Co Ltd
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Akechi Ceramics Co Ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D41/00Casting melt-holding vessels, e.g. ladles, tundishes, cups or the like
    • B22D41/50Pouring-nozzles
    • B22D41/52Manufacturing or repairing thereof
    • B22D41/54Manufacturing or repairing thereof characterised by the materials used therefor

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  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Compositions Of Oxide Ceramics (AREA)
  • Casting Support Devices, Ladles, And Melt Control Thereby (AREA)
  • Continuous Casting (AREA)
  • Treatment Of Steel In Its Molten State (AREA)

Abstract

The invention is related to a continuous casting nozzle for casting of aluminum killed steel without clogging of the bore of the nozzle. The surface layer of the bore of the continuous casting nozzle contacting with the molten steel is formed of a refractory comprising graphite from 10 to 35 wt%, an aggregate of 10 to 60 wt% selected from from alumina matter, zirconia matter, zircon matter, or alumina-silica matter and roseki containing the pyrophyllite (Al2O3.4SiO2.H2O) as the main component as the rest part of the above mentioned materials.

Description

"A.
-1- P/00/0011 Regulation 3.2
AUSTRALIA
Patents Act 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT
ORIGINAL
Name of Applicant: Actual Inventor: Address for service in Australia: Invention Title: AKECHI CERAMICS KABUSHIKI KAISHA Toshiyuki Muroi CARTER SMITH BEADLE 2 Railway Parade Camberwell Victoria 3124 Australia A CONTINUOUS CASTING NOZZLE FOR CASTING MOLTEN STEEL The following statement is a full description of this invention, including the best method of performing it known to us -2- FIELD OF THE INVENTION The present invention relates to a continuous casting nozzle for permitting effective prevention of narrowing, clogging of the nozzle bore or metal sticking to the nozzle bore through which molten steel passes in performing continuous casting of the molten steel containing aluminum such as aluminum-killed steel.
THE RELATED ART A continuous casting nozzle for casting molten steel is used for the following purposes.
As for continuous casting molten steel, a continuous casting nozzle is used for such purpose of preventing the molten steel from being oxidized by contacting with the open air and from splashing when the molten steel is poured from a tundish to a mold, and rectifying the flow of the molten steel poured for preventing non-metallic i asinclusion and slag present near or on the mold surface from being entrapped in the cast steel strand.
Material of a conventional continuous casting nozzle of molten steel comprises such material as graphite, alumina, silica, silicon carbide and recently zirconia. However, there are following problems in the case of casting aluminum-killed steel and the like.
•As for the aluminum-killed steel and the like, aluminum, which is added as i 20 a de-oxidizer, reacts with oxygen existing in the molten steel to produce non-metallic inclusion such as a-alumina. Therefore, in casting the aluminum-killed steel and the like, the non-metallic inclusion such as a-alumina adheres and accumulates onto the surface of the bore of the continuous casting nozzle, so that the bore is narrowed or clogged up in the worst case, which makes stable casting to be difficult. Furthermore, the non-metallic inclusion such as a-alumina adhered or accumulated onto the surface of the bore peels off or falls down, and is entrapped in the cast steel strand, thus degrading the quality of the cast steel strand.
For the purpose of preventing the above-mentioned reduction or clogging of the bore caused by the non-metallic inclusion such as a-alumina, there is a BGC:JL:TMP26274AKE.SPE 14 November 1997 -3commonly used method for preventing the non-metallic inclusion such as a-alumina existing in the molten steel from adhering or accumulating on the surface of the bore of the nozzle by ejecting inert gas from the inner surface of the nozzle bore toward the molten steel flowing through the bore (for example, Japanese Patent Publication No. Hei 6-59533/1994).
However, there are problems as described below for the above-mentioned method wherein inert gas is ejected from the inner surface of the nozzle.
A large amount of the ejected inert gas causes entrapment of bubbles produced by the inert gas into the cast steel strand, resulting in defects based on pinholes. On the other hand, a small amount of the ejected inert gas causes adhesion and accumulation of the non-metallic inclusion such as cc-alumina onto the surface of the bore of the nozzle, thus causing narrowing or clogging, in the worst case, of the bore.
Additionally, it is constructionally difficult to uniformly eject the inert gas from the inner surface of the nozzle bore toward the molten steel flowing through the bore. And in the case that the casting is performed in a long period of time, a stable control of the amount of ejected inert gas becomes gradually more difficult as the composition and the structure of the material consisting of the continuous casting nozzle degrades. And moreover, it becomes difficult to eject inert gas uniformly from the inner surface to the nozzle bore. As a result, the non-metallic inclusion such as a-alumina adhere and accumulate onto the surface of the bore of the nozzle so that the bore is narrowed or clogged up in the end.
It is thought that the clogging of the nozzle by the non-metallic inclusion, specially by the alumina inclusion is caused as described below.
Alumina inclusion is produced from aluminum in the steel by secondary oxidation, such as oxidation by entrapped air passing through a refractory junction and refractory structure or oxidation by supplying oxygen obtained from reduction of silica in a graphite- or carbon-containing refractory.
Alumina inclusion is produced by diffusion and cohesion of the alumina produced in the above process.
BGC:IL:TMP26274AKE.SPE 14 Novcmbcr 1997 Graphite on the surface of the nozzle bore vanishes and the surface of the bore becomes rough and thus the alumina inclusion is apt to accumulate on the rough surface of the bore.
On the other hand, as a counterplan in view of nozzle material, a nozzle in which a non-oxide raw material (SiC, Si3N, BN, ZrB,, SIALON etc.) that has low reactivity with aluminum oxide is added to alumina-graphite or a nozzle consisting of the non-oxide material itself is proposed (for example, Japanese Patent Publication No. Sho 61-38158/1986).
However, this counterplan is not practical in the case of the alumina-graphite nozzle because the adhesion preventing effect is not recognized and further corrosion resistance is decreased unless much of the non-oxide material is added.
Also, the nozzle consists of only the non-oxide material is not suitable for practical use in view of material cost and manufacturing cost, although a substantial effect is expected.
15 A nozzle consisting of graphite-oxide raw material containing CaO is proposed "for producing low-melting-point material by a reaction of CaO in an oxide raw material containing CaO (CaO.ZrO,. CaO.SiO 2 2CaO-SiO etc.) with A10, and forming the low-melting-point material in the steel (for example, Japanese Patent Laid-Open Publication No. Sho 62-56101/1987).
20 However, reactivity of CaO with AlO 3 is apt to be influenced by a temperature condition of the molten steel in casting, and there is a case that amount of CaO is not sufficiently secured for satisfying spalling resistance and corrosion resistance when plenty of AO1 2 0 inclusion is contained in the steel.
It is therefore desirable to provide a continuous casting nozzle having features of forming a glass layer at the surface of the bore of the nozzle when the nozzle is used, thereby preventing air from being entrapped through refractory structure, smoothing the bore surface of the nozzle and preventing the accumulation of alumina.
Also, a further desirable outcome of the present invention is to provide a continuous casting nozzle which prevents erosion by products having a low-melting point on account of a reaction between an aggregate in a refractory and alumina in the steel, and to provide the nozzle which is not influenced by a temperature of the molten steel RNM:JH:40372161.RS1 P4 21 December 2000 in casting, and which is able to prevent the bore from narrowing or clogging economically, comparatively easy and stable.
In one aspect of the invention, there is provided a continuous casting nozzle for casting molten steel, wherein the surface layer of the bore of said continuous casting nozzle contacting with the molten steel is formed of a refractory comprising graphite from 10 to 35 wt%, an aggregate of 10 to 60 wt% selected from alumina, zirconia, zircon, or alumina-silica and roseki containing the pyrophyllite (A1 2 0 3 -4SiO z .H0) as the main component of the above mentioned materials.
In another embodiment of the present invention, the surface layer of the bore of a continuous casting nozzle contacting with molten steel is formed of a refractory comprising graphite from 10 to 35 wt%, an aggregate of 10 to 60 wt% selected from alumina, zirconia, zircon, or alumina-silica and roseki containing the pyrophyllite (A1 2 0 3 4SiO 2
-H
2 O) as the main component as the rest part of the above mentioned materials, the said refractory being added binder, kneaded, formed, and sintered in the 15 anti-oxidizing atmosphere.
It is preferable that the roseki containing the pyrophyllite as the main e component is calcinated at a temperature equal to or more than 800 0 C so as to remove water in the crystal structure and contain alkaline component from 1 to 5 wt%. As for the roseki having above mentioned component, it is preferable that a mixing ratio by 20 weight of roseki with an average grain diameter equal to or less than 250gm is equal to or less than 60% relative to the whole of the roseki content.
*As for roseki having above mentioned component, it is preferable that the roseki containing the pyrophyllite as the main component is calcinated at a temperature equal to or more than 800 0 C so as to vanish crystal water and contains alkaline component from 1 to 5 wt Furthermore, the mixing weight ratio of roseki whose average grain diameter equal to or less than 250gm, is equal to or less than 60% relative to the whole of the roseki content. And as for the binder a thermosetting resin, for example, phenol RNM:JH:40372161.RSI P4 21 December 2000 -6resin is preferable selected. With respect to forming process CIP (Cold isostatic process) should be preferably selected.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 shows a longitudinal cross section of a nozzle according to the present invention comprising a invented refractory at the surface layer of the bore of the nozzle.
FIG. 2 shows a longitudinal cross section of a nozzle according to the present invention comprising a invented refractory at the surface layer of the bore of the nozzle and the lower part (a part immersed in the molten steel) of the nozzle.
EMBODIMENTS OF THE INVENTION A major characteristic of a continuous casting nozzle of the present invention is that the main component of a refractory of the surface layer of the bore of the nozzle is roseki. During usage, when silica in the above mentioned refractory coexisting with graphite or carbon the following reactions are usually caused.
15 SiO 2 C(S) SiO(g) CO(g) 3SiO(g) 2A1 A120 3 3Si 3CO(g) 2A1 A1 2 0 3 3C As shown in the above reactions, decomposition of the silica produces SiO(g) and CO(g), which react with aluminum in the steel to form A1 2 0 3 and it becomes the S 20 source of oxygen to the steel.
However, as for the roseki, the roseki particles do not decompose even if it is coexisting with graphite or carbon, namely SiO 2 in pyrophyllite (Al203-4SiO 2 which is the main mineral of the roseki is stable. This fact is found from the facts that the particles do not decay and bubbles are not produced, which is confirmed by means of a microscope observation after forming a briquette consisting of the roseki, resin powders and carbon powders and performing heat-treatment at a temperature of 1500 0 C for 24 hours with burying it in a coke breeze.
The half-melting temperature of the roseki is about 1500 0 C, so that it melts at the bore surface contacting with the molten steel to form a glass coat for smoothing the structure of the surface of the bore and for preventing air from being BGC:JLTMP26274AKE.SPE 14 November 1997 7entrapped through a refractory structure.
This is found from the fact that the permeability is decreased such that the permeability after performing heat-treatment at a temperature of 1500°C for 1 hours is as small as about 9.5x10- 5 darcy, in contrast the permeability after performing heat-treatment at a temperature of 1000°C for 1 hours is about 9.5x10- 4 darcy.
Although the mixing amount of the roseki is the rest part of the mixing amount of other components, a mixing weight ratio of the roseki is equal to or more than 30 wt% in order to actively form the glass coat on the surface of the bore in use as continuous casting nozzle, preferably. Also, it is preferably that the mixing weight ratio of the roseki is equal to or less than 80 wt% because degree of softening deformation is large with a range of over 80 wt%.
The most preferable mixing weight ratio of the roseki is from 30 wt% to 60 wt%.
In this case the aggregate of roseki particles does not decompose even coexisting with graphite.
15 As for kinds of roseki, it is possible to use three kinds of roseki, that is pyrophyllite matter roseki, kaolin matter roseki, and sericite matter roseki.
The pyrophyllite matter roseki with refractoriness from SK29 to SK32 (SK(Seger Se cone) is a Japanese Standard for refractoriness is suitable, considering formation of a glass layer and erosion resistance against the molten steel, as the surface of the 20 bore contacting with the molten steel is half-molten in use. Both of the kaolin matter roseki and the sericite matter roseki is not preferable because the kaolin matter roseki has a greater refractoriness from SK33 to SK36, and the sericite matter roseki has a smaller refractoriness from SK26 to SK29.
As for the binder for forming the nozzle body a thermosetting resin, for example phenol resin, is preferably used and the mixing ratio is preferably 5 to. wt%. And the most preferable process of the mixed material is CIP(cold isostatic pressing) to produce the nozzle having a high heat resistance.
Sintering of the formed body is preferably performed in the nonoxidizing atmosphere to minimize the burning loss of the graphite mixed in the material, which is mixed to enhance the erosion resistance and oxidation resistance and the BGCJL:TMP26274AKE.SPE 14 November 1997 -8sintering temperature is preferably 1000 to 1200 'C to obtain a sufficient strength of the nozzle.
The reason for using the roseki calcinated at a temperature equal to or more than 800'C to vanish crystal water is that the crystal water is released from the roseki at a temperature in a range of from 500 to 800 0 C in sintering and the refractory cracks by virtue of an unusually large coefficient of thermal expansion in this range. The alkaline component of the roseki from 1 to 5 wt% is preferable to control the melting point of roseki adequately.
It is preferable that a mixing weight ratio of roseki with an average grain diameter equal to or less than 250[tm is equal to or less than 60% relative to the whole of the roseki content because, in the range of over 60%, structural defects such as lamination are apt to be produced in molding and softening deformation of roseki particles is apt to happen when used in a continuous casting nozzle.
The half-melting temperature of the roseki is about 1500'C, and it melts at the bore 15 surface contacting with the molten steel to form a glass coat for smoothing the structure of the surface of the bore and for preventing air from being entrapped through a refractory structure, so that it has the effect to depress the adherence of A1 2 0 3 and metal.
To prevent the softening deformation and to maintain heat-impact resistance ooooo3 20 of the roseki, preferably, a mixing weight ratio of the graphite is equal to or more than 10 wt%. Also, it is preferably that the mixing weight ratio of the graphite is equal to or less than 35 wt% from the view point of manufacturing of the nozzle because the volume ratio of the graphite relative to the roseki is too large so that structural defects such as lamination are apt to be produced in the range of over wt%. Considering thermal conductivity and oxidation resistance, natural graphite is suitable as the graphite to be mixed.
As for the aggregate to be mixed, an aggregate of 10 to 60 wt% selected from alumina matter, zirconia matter, zircon matter, or alumina-silica matter should be selected, to obtain a sufficient erosion resistance of the nozzle against molten steel.
The continuous casting nozzle for steel according to the present invention will BGC:JLTMP26274AKE.SPE4 1 14 Novcmbcr 1997 -9be described in detail with reference to the accompanying drawings of nozzle for continuous casting.
As shown in FIG. 1, a surface layer 2 of the bore 1, through which the molten steel flows, of the immersion nozzle 10 consists of a refractory having the chemical composition as described above. The rest part of the nozzle 3 is composed of regular refractory, for example, of alumina-graphite which is already known in public. The dimensions of the nozzle are about 1,000mm in total length, about 60mm in diameter of the bore, 160mm in outer diameter, and about 50mm in thickness.
FIG. 2 shows another embodiment of the invention, a nozzle comprising a refractory according to the present invention at the surface layer of the bore of the nozzle and the lower part (a part immersed in the molten steel) of the nozzle. In the bore 1 of the nozzle for continuous casting, the adherence and accumulation of non-metallic oo.
inclusion such as a-alumina are depressed.
EXAMPLES
15 The present invention is explained with examples as described below.
The samples Nos. 1 to 5 (hereinafter referred to as the "sample of the present invention") having the chemical compositions within the scope of the present invention, and the samples Nos. 6 to 8 (hereinafter referred to as "sample for comparison") having chemical compositions out of the scope of the present invention were prepared as shown in Table 1, and phenol resin in the state of powder and liquid was added in an amount within a range of from 5 to 10 wt% to each of the mixed materials. From the mixed materials above, the following formed bodies were prepared.
A first formed body (hereinafter referred to as the "formed body with dimensions of 30mm by 30mm by 230mm for examining an amount of adhesion of non-metallic inclusion such as alumina and corrosion resistance against the molten steel, a second formed body (hereinafter referred to as the "formed body with dimensions of 50mm" 1 by 20mm for examining permeability, and a third formed body (hereinafter referred to as the "formed body with dimensions of 100mm in outer diameter, 60mm in inner diameter and 250mm in length for examining spalling BGC:IL:TMP26274AKE.SPE 14 November 1997 resistance, were respectively prepared, and then the bodies were sintered in reducing atmosphere at a temperature in a range from 1000 to 1200 0 C and samples 1 to 8 were prepared.
Physical properties (porosity and bulk density) for each of the above-mentioned samples of the present invention Nos. 1 to 5 and the samples for comparison Nos.
6 to 8 are shown in Table 1.
The spalling resistance of each of the sintered formed bodies 3 of the samples of the present invention Nos. 1 to 5 and the samples for comparison Nos. 6 to 8 were examined after heating at a temperature of 1500°C for 80 minutes in an electric furnace and then rapidly cooling by water. The results are shown in Table 1.
An erosion ratio and an amount of adhesion of non-metallic inclusion such as alumina of each of the sintered formed bodies 1 of the samples of the :present invention Nos. 1 to5 and the samples for comparison Nos. 6 to 8 were r examined after immersing in molten steel, which contains aluminum in a range from 0.02 to 0.05 wt%, at a temperature of 1550'C for 180 minutes. The results are shown in Table 1.
permeability for each of the sintered formed bodies 2 of the samples of the present invention Nos. 1 to 5 and the samples for comparison Nos. 6 to 8 were examined after heating at a temperature of 1500°C for 60 minutes in an electric e 20 furnace and then cooling. The results are shown in Table 1.
It is easily understood from Table 1 that the samples of the present invention are superior in the spalling resistance so the nozzle is not destroyed at the beginning of casting. Also, the non-metallic inclusion such as alumina does not adhere in spite of the low erosion ration, thereby effectively preventing narrowing or clogging of the continuous casting nozzle of the molten steel.
And also, it is possible for the samples of the present invention to prevent air from being entrapped through the refractory in practical use because of small permeability.
On the other hand, it is obvious that the sample for comparison No. 6 is remarkably inferior in the spalling resistance and the corrosion resistance against the BGC:JI.,TMP26274AKE.SPE 14 Novcmbcr 1997 11 molten steel, although a small amount of alumina adheres due to much roseki content.
As for the sample for comparison No. 7, the amount of adhesion of alumina is remarkably large, because it contains A1 2 0 3 and SiO 2 which decomposes to supply oxygen in the steel, instead of the roseki.
As for the sample for comparison No. 8, it does not contain SiO 2 instead of roseki and contains only A1 2 0 3 and it has high permeability and the amount of adhesion of alumina is remarkably large, although it contains no mineral source of oxygen to the steel.
Therefore, with the use of the continuous casting nozzle for casting steel according to the present, invention, it is possible to perform stable casting with preventing narrowing or clogging of the bore caused by the non-metallic inclusion such as alumina without deterioration of the refractory structure.
According to the present invention, approximately 300 ton of a low carbon 15 aluminum killed steel of 5 to 7 charges is continuously cast with one nozzle without clogging by 2 strand slab caster in real operation, though with conventional nozzle, clogging up in the nozzle were occurred within 2 to 4 charges under same condition.
BGCJTM26274AKSPE 14 Novmber 1997 o° BGC:JL;TMP26274AKE.SE 14 Novcmber 1997 *4 .4 4, 4* 4 4 9 4. *4 4 4 4 4 4 44 4 4 4- 4 94 4 444 4444 4444 4. *4 44.4 *4 4* 94 4 4 *4 44 4 4. 4 4 444 4 4 4 4 *4 [Table 11 Physical Properties Prmeail (xl 0%ac) Sprlliy Ressnc Amoun Ahsion ofte Atelumn Simple No. of the Present rinvention 1 2 3 4 5 10 10 20 35 25 20 i5 15 415 35 .20 1is 1 30 50 50 35 13.7 13.8 13.6 13.5 16.2 2.19 2.21 2.30 2.31 2.05 8.8 9.2 9.5 9.5 7.0 7 3 3 5 7.5 10.0 13.0 12.0 Ncrack No crack No crackNocak ocrk Sample No. for Co mparison 6 7 8 5 25 10 50 13.5 12.8 16.4 2.22 2.30 2.56 8.5 12.1 20 3 1 3.0 65 Crack N o crack Crack occurrence occurrence 15

Claims (7)

1. A continuous casting nozzle for casting molten steel, wherein the surface layer of the bore of said continuous casting nozzle contacting with the molten steel is formed of a refractory comprising graphite from 10 to 35 wt%, an aggregate of 10 to 60 wt% selected from alumina, zirconia, zircon, or alumina-silica and roseki containing the pyrophyllite (A1 2 0 3 4SiO 2 as the main component of the above mentioned materials.
2. A continuous casting nozzle for casting molten steel, wherein the surface layer of the bore of said continuous casting nozzle contacting with the molten steel is formed of a refractory comprising graphite from 10 to 35 wt%, an aggregate of 10 to 60 wt% selected from alumina, zirconia, zircon, or alumina-silica and roseki containing the .pyrophyllite (Al,0 3 -4SiO 2 -HO) as the main component of the above mentioned materials, the said refractory being added binder, kneaded, formed, and sintered in the 15 anti-oxidizing atmosphere.
3. A continuous casting nozzle according to claim 1 or 2, wherein the roseki containing the pyrophyllite as the main component, is calcinated at a temperature equal to or more than 800 0 C so as to remove the water component in the crystal 20 structure and contains alkaline component from 1 to 5 wt%.
4. A continuous casting nozzle according to claim 2, wherein a mixing ratio by weight of the roseki, whose average grain diameter equal to or less than 250ptm, is equal to or less than 60% relative to the whole of the roseki content.
A continuous casting nozzle according to claim 2, wherein said binder is a thermosetting resin.
6. A continuous casting nozzle according to claim 2, wherein said forming process is CIP process. RNM:JH:40372161.RSI CLMS 21 December 2000 14
7. A continuous casting nozzle substantially as hereinbefore described with reference to the accompanying drawings. DATED: 21 December 2000 FREEHILLS CARTER SMITH BEADLE Patent Attorneys for the Applicant: AKECI-II CERAMICS KABUSJ{IKI KAISHA RNM:JH:40372 161 .RS 1 CLMS 2 eebr20 21 December 2000
AU45229/97A 1996-12-05 1997-11-14 A continuous casting nozzle for casting molten steel Ceased AU730801B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP8342597A JPH10166116A (en) 1996-12-05 1996-12-05 Nozzle for continuous casting
JP8-342597 1996-12-05

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Publication Number Publication Date
AU4522997A AU4522997A (en) 1998-06-11
AU730801B2 true AU730801B2 (en) 2001-03-15

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EP (1) EP0846514B1 (en)
JP (1) JPH10166116A (en)
AT (1) ATE198172T1 (en)
AU (1) AU730801B2 (en)
CA (1) CA2223356C (en)
DE (1) DE69703729T2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2959632B1 (en) * 1998-07-09 1999-10-06 明智セラミックス株式会社 Nozzle for continuous casting
DE69920709T2 (en) * 1999-04-05 2006-02-09 Tokyo Yogyo K.K. continuous casting
AU748092B2 (en) 1999-04-09 2002-05-30 Akechi Ceramics Kabushiki Kaisha Continuous casting nozzle
DE60040047D1 (en) 1999-10-28 2008-10-09 Fujifilm Corp Optical wavelength conversion system and wavelength stabilized laser
JP2014073528A (en) * 2012-09-11 2014-04-24 Akechi Ceramics Co Ltd Continuous casting nozzle

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6278151A (en) * 1985-09-28 1987-04-10 新日本製鐵株式会社 Non-burnt refractory brick for molten metal vessel
US4989762A (en) * 1989-02-07 1991-02-05 Akechi Ceramics Co., Ltd. Molten steel pouring nozzle
US5046647A (en) * 1987-09-03 1991-09-10 Toshiba Ceramics Co., Ltd. Nozzle for discharging molten metal used in a casting device

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Publication number Priority date Publication date Assignee Title
GB1239458A (en) * 1968-07-31 1971-07-14
JPS5641871A (en) * 1979-09-13 1981-04-18 Akechi Taikarenga Kk Continuously casting immersion nozzle
JPS62148076A (en) * 1985-12-23 1987-07-02 Akechi Ceramics Kk Nozzle for continuous casting
GB2202218B (en) * 1987-02-19 1991-02-06 De Beers Ind Diamond Method of making an article from pyrophyllite

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6278151A (en) * 1985-09-28 1987-04-10 新日本製鐵株式会社 Non-burnt refractory brick for molten metal vessel
US5046647A (en) * 1987-09-03 1991-09-10 Toshiba Ceramics Co., Ltd. Nozzle for discharging molten metal used in a casting device
US4989762A (en) * 1989-02-07 1991-02-05 Akechi Ceramics Co., Ltd. Molten steel pouring nozzle

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CA2223356C (en) 2002-07-23
JPH10166116A (en) 1998-06-23
AU4522997A (en) 1998-06-11
EP0846514A1 (en) 1998-06-10
DE69703729T2 (en) 2001-04-19
DE69703729D1 (en) 2001-01-25
CA2223356A1 (en) 1998-06-05
ATE198172T1 (en) 2001-01-15
EP0846514B1 (en) 2000-12-20

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