WO1996036575A2 - Process for production of alumina/zirconia materials - Google Patents

Process for production of alumina/zirconia materials Download PDF

Info

Publication number
WO1996036575A2
WO1996036575A2 PCT/US1996/005145 US9605145W WO9636575A2 WO 1996036575 A2 WO1996036575 A2 WO 1996036575A2 US 9605145 W US9605145 W US 9605145W WO 9636575 A2 WO9636575 A2 WO 9636575A2
Authority
WO
WIPO (PCT)
Prior art keywords
alumina
zirconia
melt
azs
weight
Prior art date
Application number
PCT/US1996/005145
Other languages
French (fr)
Other versions
WO1996036575A3 (en
Inventor
Peter J. Ashley
Original Assignee
Saint-Gobain Industrial Ceramics, Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Saint-Gobain Industrial Ceramics, Inc. filed Critical Saint-Gobain Industrial Ceramics, Inc.
Priority to AT96912746T priority Critical patent/ATE187979T1/en
Priority to DE69605785T priority patent/DE69605785T2/en
Priority to AU55447/96A priority patent/AU5544796A/en
Priority to EP96912746A priority patent/EP0823934B1/en
Publication of WO1996036575A2 publication Critical patent/WO1996036575A2/en
Publication of WO1996036575A3 publication Critical patent/WO1996036575A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/16Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay
    • C04B35/18Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay rich in aluminium oxide
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/16Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/14Anti-slip materials; Abrasives
    • C09K3/1409Abrasive particles per se
    • C09K3/1427Abrasive particles per se obtained by division of a mass agglomerated by melting, at least partially, e.g. with a binder

Definitions

  • This invention relates to fused alumina/zirconia materials which have found wide applicability, especially in the field of abrasives.
  • the invention relates particularly to a process for making such materials that has significant cost advantages over those currently practiced in the art. It is well known from patents such as USPP 3,454,385;
  • alumina and zirconia can be co-fused in the same vessel and then formed in to very useful abrasive grains, particularly when the process is manipulated to ensure that the zirconia in obtained in the tetragonal form.
  • the very high cost of the zirconia component has made it difficult for the grain to be as widely accepted as its undoubted utility as an abrasive would seem to justify.
  • the present invention provides a process for the production of alumina/zirconia abrasives which comprises forming a melt comprising alumina/zirconia/silica (AZS) scrap, adding to the melt an amount of a reducing agent sufficient to reduce the silica content to a level below about 0.8% by weight and then forming abrasive grits from the melt.
  • alumina/zirconia abrasives which comprises forming a melt comprising alumina/zirconia/silica (AZS) scrap, adding to the melt an amount of a reducing agent sufficient to reduce the silica content to a level below about 0.8% by weight and then forming abrasive grits from the melt.
  • AZS scrap refers to waste material generated as a result of the use of large AZS blocks to line glass furnaces. Periodically these linings have to be replaced and the discarded blocks of AZS become scrap to be disposed of as economically as possible.
  • the original composition of AZS blocks used to line glass furnaces is from about 48 to about 50 wt% of alumina; from about 30 to about 35 wt% of zirconia; and from about 12 to about 18 wt% of silica.
  • Scrap generated in the production of such blocks is one preferred source of AZS scrap.
  • Scrap generated when such blocks are replaced is a secondary though occasionally less desirable source.
  • the AZS blocks may become contaminated with up to about 2-3% of glass.
  • Certain components of the glass such as silica and soda can be quite detrimental to the abrasive properties of any grains produced from such starting materials unless special precautions are taken to eliminate them, or at least to reduce them to acceptable levels during the production process.
  • Other components such lead, (when the glass produced in the furnace is a lead crystal) , produce other very significant environmental problems such that AZS contaminated in this way is very much less preferred as a feedstock.
  • AZS scrap materials can be used effectively, either alone or in admixture with appropriate amounts of alumina and zirconia to adjust the final composition to the desired alumina/zirconia ratio, if a reducing agent selected from the group consisting of carbon, aluminum, magnesium, zirconium and mixtures of the above is added to a melt of the AZS and any other starting materials in an amount sufficient toreduce the silica content of the final product to below 0.8 wt% and more preferably below 0.4wt%.
  • This amount will depend on the amount of impurity in the AZS and the silica content of the AZS itself. However for most purposes an amount that is from about 5 to about 30%, and more preferably from about 10 to about 20%, based on the weight of the molten components, may be used with advantage.
  • the preferred reducing agents are carbon and aluminum and mixtures of these. Magnesium and zirconium both raise handling problems and for that reason are less preferred.
  • the most preferred reducing agent is a mixture of carbon and aluminum in a weight ratio of from 1:0 to 1:2.
  • the reducing agent chosen was a mixture of carbon and aluminum metal in the form of chips.
  • the AZS fed in to the melt comprised about 49% alumina, about 37% zirconia and about 14% silica, all proportions being by weight.
  • the AZS scrap did not have any glass contamination.
  • the zirconia content of the materials made in the following Examples was to be at least 25% by weight.
  • all the zirconia was supplied by AZS scrap and the reducing agent used was carbon alone in the form of petroleum coke.
  • the feed comprised alumina, AZS scrap and coke.
  • the same AZS scrap used in Example 1 was used in this Example.
  • the coke was added in two increments: the first, (I), with the feedstock and the second, (II) , during the "fuseout" period after the molten mass had been formed but before the molten mass was tapped off and the cooling process had begun.
  • the results are set forth in Table 2 below.
  • the Power value for Test “A” includes the energy used to start and heat up the furnace.
  • the high value for Test “D” results from the small amount of the product tapped from the furnace due to the presence of unburned carbon in the melt because of the small size of the furnace. Such conditions would not be created in a production-size furnace. It is considered that, at steady state operations, a power consumption of around 2 K H per pound of grain produced is enirely achievable.

Abstract

A process is described for the production of alumina/zirconia materials which uses cheap scrap alumina/zirconia/silica material as feedstock along with a reducing agent to lower the final silica content to an acceptable level.

Description

PROCESS FOR PRODUCTION OF ALUMINA/ZIRCONIA MATERIALS
Background of the Invention This invention relates to fused alumina/zirconia materials which have found wide applicability, especially in the field of abrasives. The invention relates particularly to a process for making such materials that has significant cost advantages over those currently practiced in the art. It is well known from patents such as USPP 3,454,385;
3,891,408; 4,454,767 and 5,143,522 that alumina and zirconia can be co-fused in the same vessel and then formed in to very useful abrasive grains, particularly when the process is manipulated to ensure that the zirconia in obtained in the tetragonal form. However the very high cost of the zirconia component has made it difficult for the grain to be as widely accepted as its undoubted utility as an abrasive would seem to justify.
A process has now been discovered that enables a very low cost source of zirconia to be used, thus making this very valuable abrasive grain accessible at a more moderate price. General Description of the Invention
The present invention provides a process for the production of alumina/zirconia abrasives which comprises forming a melt comprising alumina/zirconia/silica (AZS) scrap, adding to the melt an amount of a reducing agent sufficient to reduce the silica content to a level below about 0.8% by weight and then forming abrasive grits from the melt.
"AZS scrap" as the term is used herein refers to waste material generated as a result of the use of large AZS blocks to line glass furnaces. Periodically these linings have to be replaced and the discarded blocks of AZS become scrap to be disposed of as economically as possible. The original composition of AZS blocks used to line glass furnaces is from about 48 to about 50 wt% of alumina; from about 30 to about 35 wt% of zirconia; and from about 12 to about 18 wt% of silica.
Scrap generated in the production of such blocks is one preferred source of AZS scrap. Scrap generated when such blocks are replaced is a secondary though occasionally less desirable source. During use the AZS blocks may become contaminated with up to about 2-3% of glass. Certain components of the glass such as silica and soda can be quite detrimental to the abrasive properties of any grains produced from such starting materials unless special precautions are taken to eliminate them, or at least to reduce them to acceptable levels during the production process. Other components such lead, (when the glass produced in the furnace is a lead crystal) , produce other very significant environmental problems such that AZS contaminated in this way is very much less preferred as a feedstock.
It has now been found that AZS scrap materials can be used effectively, either alone or in admixture with appropriate amounts of alumina and zirconia to adjust the final composition to the desired alumina/zirconia ratio, if a reducing agent selected from the group consisting of carbon, aluminum, magnesium, zirconium and mixtures of the above is added to a melt of the AZS and any other starting materials in an amount sufficient toreduce the silica content of the final product to below 0.8 wt% and more preferably below 0.4wt%. This amount will depend on the amount of impurity in the AZS and the silica content of the AZS itself. However for most purposes an amount that is from about 5 to about 30%, and more preferably from about 10 to about 20%, based on the weight of the molten components, may be used with advantage.
The preferred reducing agents are carbon and aluminum and mixtures of these. Magnesium and zirconium both raise handling problems and for that reason are less preferred. The most preferred reducing agent is a mixture of carbon and aluminum in a weight ratio of from 1:0 to 1:2.
Description of Preferred Embodiments
The invention is now described with particular reference to the following Examples which are for the purposes of illustration only and are intended to imply no essential limitation on the scope of the invention. Example 1
In a conventional process for the manufacture of an alumina/zirconia abrasive using a fusion mixture of 35% by weight of zirconia and 64% by weight of alumina, varying proportions of the conventional alumina/zirconia feed were replaced by AZS scrap.
The reducing agent chosen was a mixture of carbon and aluminum metal in the form of chips.
The AZS fed in to the melt comprised about 49% alumina, about 37% zirconia and about 14% silica, all proportions being by weight. The AZS scrap did not have any glass contamination.
Five runs were performed with varying amounts of the total normal alumina/zirconia charge replaced by AZS scrap. The abrasive grits obtained were analyzed and the power used to process the melt, (a measure of the efficiency of the process) , was measured. The results are set out in Table 1 below.
Table 1
AZS in FEED KWH/lb Si02 Na20 Zr02 C/Al*
20% 1.7 0.36 0.03 32.2 4/4
40% 1.7 0.55 0.04 34.0 4/4
60% 1.7 0.65 0.04 33.5 6/6
80% 1.7 0.57 0.04 34.6 6/8
100% 2.1 0.54 0.03 32.4 8/10
* expressed in terms of the percentage of the total weight of the feedstock represented by each component.
From the above data it is clear that an alumina/zirconia feedstock comprising impure AZS scrap can be used and the critical silica and soda contents can be controlled, providing appropriate amounts of suitable reducing agents are used. Example 2
The zirconia content of the materials made in the following Examples was to be at least 25% by weight. In the Examples, all the zirconia was supplied by AZS scrap and the reducing agent used was carbon alone in the form of petroleum coke. Thus the feed comprised alumina, AZS scrap and coke. The same AZS scrap used in Example 1 was used in this Example.
The coke was added in two increments: the first, (I), with the feedstock and the second, (II) , during the "fuseout" period after the molten mass had been formed but before the molten mass was tapped off and the cooling process had begun. The results are set forth in Table 2 below.
Table 2
MATERIAL ADDED Test A Test B Test C Test D
Alumina 19.5 19.5 19.5 19.5
AZS 36.75 36.75 36.75 36.75
Coke (I) 1 1 1.5 1.5
Coke (II) 1 1.5 1 1.5
RESULTS
Silica 0.59 0.58 0.63 0.31
Zirconia 28.9 28.5 29.5 23.4
Power (KWH/lb) 3.45 2.06 2.04 2.78
The Power value for Test "A" includes the energy used to start and heat up the furnace. The high value for Test "D" results from the small amount of the product tapped from the furnace due to the presence of unburned carbon in the melt because of the small size of the furnace. Such conditions would not be created in a production-size furnace. It is considered that, at steady state operations, a power consumption of around 2 K H per pound of grain produced is enirely achievable.

Claims

1. A process for the production of an alumina/zirconia material which comprises forming a melt comprising AZS scrap and adding to the melt an amount of a reducing agent sufficient to reduce the silica content to a level below about 1.0% by weight.
2. A process according to Claim 1 in which alumina and/or zirconia are also added to the melt to produce an alumina/zirconia material with the desired composition.
3. A process according to Claim 1 in which the reducing agent is selected from the group consisting of carbon, aluminum, magnesium, zirconium and mixtures thereof.
4. A process according to Claim 1 in which the reducing agent is added in an amount that is from about 10 to about 20% of the weight of the melt.
5. A process according to Claim 1 in which the AZS scrap comprises from about 48 to about 50% alumina, from about 30 to about 35% of zirconia and from about 12 to about 18% of silica, all percentages being by weight.
6. A process for the production of an alumina/zirconia abrasive grits which comprises forming a melt comprising AZS scrap which comprises from about 48 to about 50% alumina, from about 32 to about 37% of zirconia and from about 12 to about 15% of silica, (all percentages being by weight) , and adding to the melt an amount of a reducing agent sufficient to reduce the silica content of the melt to a level below about 1.0% by weight and then casting the melt into blocks and comminuting said blocks to form abrasive grits.
7. A process according to Claim 6 in which the reducing agent is selected from the group consisting of carbon, aluminum, magnesium, zirconium and mixtures thereof.
8. A process according to Claim 6 in which the reducing agent is added in an amount that is from about 4 to about 20% of the weight of the melt.
PCT/US1996/005145 1995-05-03 1996-04-12 Process for production of alumina/zirconia materials WO1996036575A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
AT96912746T ATE187979T1 (en) 1995-05-03 1996-04-12 METHOD FOR PRODUCING MATERIALS CONTAINING ALUMINUM AND ZIRCONIA
DE69605785T DE69605785T2 (en) 1995-05-03 1996-04-12 METHOD FOR THE PRODUCTION OF ALUMINA AND ZIRCONIA CONTAINING MATERIALS
AU55447/96A AU5544796A (en) 1995-05-03 1996-04-12 Process for production of alumina/zirconia materials
EP96912746A EP0823934B1 (en) 1995-05-03 1996-04-12 Process for production of alumina/zirconia materials

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/434,087 US5567214A (en) 1995-05-03 1995-05-03 Process for production of alumina/zirconia materials
US08/434,087 1995-05-03

Publications (2)

Publication Number Publication Date
WO1996036575A2 true WO1996036575A2 (en) 1996-11-21
WO1996036575A3 WO1996036575A3 (en) 1997-03-13

Family

ID=23722775

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1996/005145 WO1996036575A2 (en) 1995-05-03 1996-04-12 Process for production of alumina/zirconia materials

Country Status (8)

Country Link
US (1) US5567214A (en)
EP (1) EP0823934B1 (en)
AT (1) ATE187979T1 (en)
AU (1) AU5544796A (en)
DE (1) DE69605785T2 (en)
TW (1) TW340835B (en)
WO (1) WO1996036575A2 (en)
ZA (1) ZA963097B (en)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2872157B1 (en) * 2004-06-24 2006-10-13 Saint Gobain Ct Recherches FROZEN ALUMINA-ZIRCONE GRAIN MIXTURE
EP2221286B1 (en) * 2007-12-06 2014-03-12 Agc Ceramics Co., Ltd. Process for producing refractory particles
CN101560074B (en) * 2008-04-16 2012-11-21 万方 Water reducer produced by utilizing zirconium silica residues and production method thereof
BR112013016734A2 (en) 2010-12-31 2019-09-24 Saint Gobain Ceramics abrasive particles with particular shapes and methods of deformation of such particles
WO2013003831A2 (en) 2011-06-30 2013-01-03 Saint-Gobain Ceramics & Plastics, Inc. Liquid phase sintered silicon carbide abrasive particles
US8986409B2 (en) 2011-06-30 2015-03-24 Saint-Gobain Ceramics & Plastics, Inc. Abrasive articles including abrasive particles of silicon nitride
US9517546B2 (en) 2011-09-26 2016-12-13 Saint-Gobain Ceramics & Plastics, Inc. Abrasive articles including abrasive particulate materials, coated abrasives using the abrasive particulate materials and methods of forming
CN104114664B (en) 2011-12-30 2016-06-15 圣戈本陶瓷及塑料股份有限公司 Form molding abrasive grains
EP3517245B1 (en) 2011-12-30 2023-12-13 Saint-Gobain Ceramics & Plastics Inc. Shaped abrasive particle and method of forming same
CN104114327B (en) 2011-12-30 2018-06-05 圣戈本陶瓷及塑料股份有限公司 Composite molding abrasive grains and forming method thereof
WO2013106602A1 (en) 2012-01-10 2013-07-18 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having particular shapes and methods of forming such particles
CA2987793C (en) 2012-01-10 2019-11-05 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having complex shapes and methods of forming same
US9242346B2 (en) 2012-03-30 2016-01-26 Saint-Gobain Abrasives, Inc. Abrasive products having fibrillated fibers
KR101888347B1 (en) 2012-05-23 2018-08-16 생-고뱅 세라믹스 앤드 플라스틱스, 인코포레이티드 Shaped abrasive particles and methods of forming same
BR112014032152B1 (en) 2012-06-29 2022-09-20 Saint-Gobain Ceramics & Plastics, Inc ABRASIVE PARTICLES HAVING PARTICULAR FORMATS AND ABRASIVE ARTICLES
CN104822494B (en) 2012-10-15 2017-11-28 圣戈班磨料磨具有限公司 The method of abrasive particle and this particle of formation with given shape
WO2014106173A1 (en) 2012-12-31 2014-07-03 Saint-Gobain Ceramics & Plastics, Inc. Particulate materials and methods of forming same
CN107685296B (en) 2013-03-29 2020-03-06 圣戈班磨料磨具有限公司 Abrasive particles having a particular shape, methods of forming such particles, and uses thereof
TW201502263A (en) 2013-06-28 2015-01-16 Saint Gobain Ceramics Abrasive article including shaped abrasive particles
WO2015048768A1 (en) 2013-09-30 2015-04-02 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
JP6290428B2 (en) 2013-12-31 2018-03-07 サンーゴバン アブレイシブズ,インコーポレイティド Abrasive articles containing shaped abrasive particles
US9771507B2 (en) 2014-01-31 2017-09-26 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle including dopant material and method of forming same
BR112016023880A2 (en) 2014-04-14 2017-08-15 Saint Gobain Ceramics abrasive article including molded abrasive particles
AU2015247826A1 (en) 2014-04-14 2016-11-10 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
WO2015184355A1 (en) 2014-05-30 2015-12-03 Saint-Gobain Abrasives, Inc. Method of using an abrasive article including shaped abrasive particles
US9914864B2 (en) 2014-12-23 2018-03-13 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and method of forming same
US9707529B2 (en) 2014-12-23 2017-07-18 Saint-Gobain Ceramics & Plastics, Inc. Composite shaped abrasive particles and method of forming same
US9676981B2 (en) 2014-12-24 2017-06-13 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle fractions and method of forming same
WO2016161157A1 (en) 2015-03-31 2016-10-06 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
TWI634200B (en) 2015-03-31 2018-09-01 聖高拜磨料有限公司 Fixed abrasive articles and methods of forming same
JP2018516767A (en) 2015-06-11 2018-06-28 サン−ゴバン セラミックス アンド プラスティクス,インコーポレイティド Abrasive articles containing shaped abrasive particles
EP4071224A3 (en) 2016-05-10 2023-01-04 Saint-Gobain Ceramics and Plastics, Inc. Methods of forming abrasive articles
EP4349896A2 (en) 2016-09-29 2024-04-10 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
US10563105B2 (en) 2017-01-31 2020-02-18 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10759024B2 (en) 2017-01-31 2020-09-01 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10865148B2 (en) 2017-06-21 2020-12-15 Saint-Gobain Ceramics & Plastics, Inc. Particulate materials and methods of forming same
CN107541189A (en) * 2017-08-22 2018-01-05 郑州威源新材料有限公司 A kind of production method for ensureing that fused alumina zirconia abrasive grain composition is stable
KR20220116556A (en) 2019-12-27 2022-08-23 세인트-고바인 세라믹스 앤드 플라스틱스, 인크. Abrasive articles and methods of forming same

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB150116A (en) * 1919-06-18 1920-09-02 Otis Hutchins An improved process for purifying aluminous materials
DE1205882B (en) * 1961-09-08 1965-11-25 Carborundum Co Process for producing an abrasive grain from aluminum oxide and zirconium oxide
US3781172A (en) * 1970-12-14 1973-12-25 G Kinney Process for the manufacture of microcrystalline fused abrasives
US3891408A (en) * 1972-09-08 1975-06-24 Norton Co Zirconia-alumina abrasive grain and grinding tools
US5143522B1 (en) * 1979-11-09 1998-01-06 Washington Mills Electro Miner Abrasive products containing fused alumina zirconia and reduced titania
FR2499061A1 (en) * 1981-01-30 1982-08-06 Sofrem METHOD AND APPARATUS FOR RAPID CONTINUOUS CASTING SOLIDIFICATION AND COOLING OF MOLDED OXIDES BASED ON METAL OXIDES
US4457767A (en) * 1983-09-29 1984-07-03 Norton Company Alumina-zirconia abrasive
AT379979B (en) * 1984-08-01 1986-03-25 Treibacher Chemische Werke Ag METHOD FOR PRODUCING ABRASIVES
JPS62100412A (en) * 1985-10-25 1987-05-09 Japan Carlit Co Ltd:The Production of alumina-zirconia compound powder body
US5183610A (en) * 1987-07-22 1993-02-02 Cooper Indusries, Inc. Alumina-zirconia ceramic
US4992396A (en) * 1987-12-16 1991-02-12 Corhart Refractories Corporation Fused AZS refractory composition
US5214011A (en) * 1991-08-30 1993-05-25 Bfd, Incorporated Process for preparing ceramic-metal composite bodies

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None

Also Published As

Publication number Publication date
ZA963097B (en) 1996-10-24
DE69605785D1 (en) 2000-01-27
EP0823934B1 (en) 1999-12-22
TW340835B (en) 1998-09-21
US5567214A (en) 1996-10-22
ATE187979T1 (en) 2000-01-15
DE69605785T2 (en) 2000-07-27
EP0823934A2 (en) 1998-02-18
WO1996036575A3 (en) 1997-03-13
AU5544796A (en) 1996-11-29

Similar Documents

Publication Publication Date Title
US5567214A (en) Process for production of alumina/zirconia materials
EP0140164B1 (en) Alumina-zirconia abrasive
CN101362651B (en) Formula of mullite light heat insulating brick
CN101066837B (en) Environment friendly heat resistant opal crystalline glass and its preparation process
US2535526A (en) Stabilized zirconia and method for producing same
KR100770678B1 (en) Fused and cast azs products of reduced cost, and uses thereof
CN100406411C (en) A composite electro-fusing refractory material and method for preparing the same
US3001881A (en) Pre-reacted glass batch and method for producing same
GB2024799A (en) Fused refractory
EP0104025A2 (en) Baddeleyite sinterable refractory compositions and refractories produced therefrom
CN102126865A (en) Method for producing high-purity fused mullite
CN115432932B (en) Glass fiber composition with ultrahigh specific modulus and glass fiber
US1966407A (en) Corundum product and process of producing the same
KR100875449B1 (en) Low-temperature solvent composition for steel refining using hand slag
EP0633232A1 (en) Fused zirconia refractory materials, method for producing the same and refractory products
US2903373A (en) Fused cast zirconia-alumina articles
US3849532A (en) Method of preparing a zirconium oxide that is crystallized mostly or completely in cubic form
US3264123A (en) Fused cast refractory
US3230101A (en) Fused cast refractory and method of making
KR960010591B1 (en) Flux for steel-making
US4366257A (en) Process for producing a calcia clinker
US1811314A (en) Refractory material
CN114293257B (en) Preparation method of novel blue single-crystal corundum and novel blue single-crystal corundum
US3251659A (en) Producing crystalline calcium oxide in an electric arc furnace
CN117362015B (en) High-purity corundum brick and preparation method thereof

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AU BR CA CN JP KR MX RU

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
AK Designated states

Kind code of ref document: A3

Designated state(s): AU BR CA CN JP KR MX RU

AL Designated countries for regional patents

Kind code of ref document: A3

Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 1996912746

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 1996912746

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: CA

WWG Wipo information: grant in national office

Ref document number: 1996912746

Country of ref document: EP