WO1988006575A1 - Process for the preparation of aluminium oxide ceramics having increased abrasion resistance - Google Patents

Process for the preparation of aluminium oxide ceramics having increased abrasion resistance Download PDF

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Publication number
WO1988006575A1
WO1988006575A1 PCT/HU1987/000009 HU8700009W WO8806575A1 WO 1988006575 A1 WO1988006575 A1 WO 1988006575A1 HU 8700009 W HU8700009 W HU 8700009W WO 8806575 A1 WO8806575 A1 WO 8806575A1
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WO
WIPO (PCT)
Prior art keywords
weight
aluminium oxide
oxide
magnesium
fluoride
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.)
Ceased
Application number
PCT/HU1987/000009
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English (en)
French (fr)
Inventor
László SZTANKOVICS
Béla LÁNYI
Tibor Fazekas
Béla TOPLAK
István SÁRKÖZI
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Olajipari Fo^"vallalkozo Es Tervezo^" Vallalat
Original Assignee
Olajipari Fo^"vallalkozo Es Tervezo^" Vallalat
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 Olajipari Fo^"vallalkozo Es Tervezo^" Vallalat filed Critical Olajipari Fo^"vallalkozo Es Tervezo^" Vallalat
Priority to AT904187A priority Critical patent/AT393120B/de
Priority to DE19873790916 priority patent/DE3790916T1/de
Priority to PCT/HU1987/000009 priority patent/WO1988006575A1/en
Priority to NL8720112A priority patent/NL8720112A/nl
Priority to CH421788A priority patent/CH677110A5/de
Priority to JP87501685A priority patent/JPH01502426A/ja
Publication of WO1988006575A1 publication Critical patent/WO1988006575A1/en
Priority to GB8826043A priority patent/GB2209334B/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • C04B35/10Shaped 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 aluminium oxide
    • C04B35/111Fine ceramics
    • 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
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64Burning or sintering processes

Definitions

  • This invention relatea to a proceaa for the preparation of aluminium oxide ceramics having increaaed abrasion resistance.
  • the said ceramics are particularly useful in the production of cylinder liners of drilling slime and slurry pumps.
  • aluminium oxide baaed ceramics suitable for various purposes (e.g. electrotechnical, thermal technical, optical, mechanical and chemical fields of application)
  • several basic materials are used (aluminas and raw materials of high purity) to which additives decreasing the sintering temperature are admixed.
  • transparent and abrasion resistant ceramics may be prepared by the process disclosed in UK patent No. 1,264,914 by introducing 1 % by weight of MgO + CeO 2 and carrying out sintering at a temperature of about 1700 o C in hydrogen or in vacuo.
  • pure magnesium oxide is incorporated (Hungarian patent No. 184,381 and UK patent No. 1,256,966); however, the addition of magnesium oxide per se only results in the inhibition of partic le-size growth at a temperature of above 1700 °C while the aintering temperature can not be decreaaed below the said value.
  • Similar results are obtained by admixing yttrium oxide (Y 2 O 3 ) per se. /Amer. Cer.
  • guillotines of high quality can be manufactured from aluminium oxide by introducing 30 % by weight of titanium carbide /Amer. Ceram. Bull. 62, /12/, 1384 (1983)/ and carrying out hot isostatic pressing.
  • a further process is disclosed in US patent No. 4,357,427 but the said method requires the use of an isostatic press.
  • a presa operating in three dimensions and a special so-called "reactive" aluminium oxide (Reinolds RC-HP) are used simultaneously and cutting tools are prepared by sintering twice at a temperature of about 1510 °C /Amer. Ceram. Bull. 61, /12/, 1311 (1982)/.
  • Disclosure of the invention It is the object of the present invention to provide a simple, readily feasible and unexpensive process for the preparation of aluminium oxide ceramics having increased abrasion resistance.
  • the said object can be achie ved by adding to 96-99.5 % by weight of aluminium oxide in an amount of 0.1-4 % by weight an eutectic sintering additive prepared from 38.5-71.5 % by weight of calcium fluoride and 28.5-61.5 % by weight of magnesium fluoride by thermal treatment and, if necessary, 0.1-1.0 % by weight of a particle-size growth inhibitor and 0.2-1.5 % by weight of a further useful additive; grinding the components; forming the mixture in a manner known per se; and aintering the shaped articles at a temperature above 1300 °C, preferably at 1450-1600 °C.
  • the present invention is based on the recognition that eutectic mixtures of calcium fluoride (mp.: 1410 °C) formed with magnesium fluoride (mp. : 1252 °C) of various compositions - used either per se or in the presence of other additives - continuously promote from a tempera ture of 980-1150 °C the recrystallization of the crystalline particles of aluminium oxide, which becomes definite in temperature-range of 1450-1600 °C.
  • the effect of the eutectic sintering additive of the present invention can be explained in a simplified manner as follows: the said sintering additive reacts with aluminium oxide in the melt phase and dissolves in the boundary surface of the aluminium oxide cryatala under thermal effect.
  • the thus activated aluminium oxide crystals - which closely contact - easily dissolve in each other under further thermal effect, whereby the crystalparticles grow, the inter-crystals pores get cloaed and consequently the system continuously sinters.
  • the process of sintering - contrary to the so-called solid-phase reaction of metal oxidea having high melting point - takes place gradually and continuously from 980 o C to about 1600 °C.
  • the fluoride system having the composition according to the present invention participates at the reaction not at once but as a function of the changes of state depending on the rising temperature.
  • sintering begins already at low temperature (small thermal expension), takes place continuously and is finished at relatively low upper temperature.
  • other reactions take place as well; e.g. under the effect of the rising temperature the split hydrated part of magnesium fluoride is converted into magnesium oxide, about 10 mole% thereof is dissolved in magnesium fluoride and at the same time fluorine leaves the system.
  • magnesium oxide inhibits the formation of coarse particles.
  • the minimal amount of nascent fluorine promotes the formation of stable alpha- corundum already at a temperature below 1000 o C in a manner being characteristic of halogens.
  • the major amount of the eutectic sintering additive is incorporated into the aluminium oxide ceramics partly because the boiling point of the components is highly above 2250 °C and particularly since it forms a solid solution with aluminium oxide.
  • a minor part of the said additive sublimates from the mixture, particularly from the boundar surface of the shaped article.
  • the eutectic sintering additive strongly increases the crystal size as a function of the temperature, in order to decrease this effect it is expedient but not necessary to use a particle-size growth inhibitor.
  • the said additives inhibiting the growth of the crystals magnesium spinel acting at lower temperature (MgAl 2 O 4 ), magnesium oxide (MgO) and nickel oxide (NiO) proved to be the most active, namely in an amount of 0.1-1.0 % by weight.
  • the calcium-magnesium-fluoride sintering additive according to the present invention significantly increases the abrasion resistance of aluminium oxide ceramics (this can be simply determined either by grinding corundum powder with alumina grinding calls for 100 hours and weighing the said grinding balls before and after the test or by comparing the operating hours of various slime pumps).
  • the abrasion resistance and to a considerable extent also the thermal shock resistance (i.e. the lifetime) of aluminium oxide ceramics can be further increased by introducing additives which react with aluminium oxide either difficultly or only at higher temperature.
  • the aaid additives are generally used in an amount of 0.2--1.5 % by weight, depending on the type thereof.
  • chrome oxide Cr 2 O 3
  • cerium oxide CeO 2
  • cerium oxide CeO 2
  • cerium oxide ZrSiO 4
  • calcium feldspar Al 2 O 3 .2SiO 2 , mp.: 1555 °C
  • alundum Al 2 O 3
  • alundum Al 2 O 3
  • alundum used e.g. in an amount of 20 % by weight which decreases the rate of shrinkage and by embedding coarse crystal particles enables the preparation of ceramics having a specially big size and a rough surface (in the latter case alundum is actually not an additive but one part of the aluminium oxide used is applied in the form of alundum). It is evident that a mixture of the said additives can be used as well.
  • the additive magnesium spinel (MgAl 2 O 4 ) used as particle- size growth inhibitor and the zirconium silicate optionally used as additive can be prepared by known methods by firing a stochiometrical amount of a metal salt or metal oxide thereof and finely grinding the fired product.
  • the optional additives may modify the properties of aluminium oxide ceramics.
  • the dry or wet abrasion resistance can be increased or the resistance of abrasion combined with thermal effects can be raised etc.
  • the eutectic sintering additives used according to the process of the present invention can be introduced either per se or can be applied onto a carrier. It is preferred to use aluminium oxide as carrier. One may preferably apply the eutectic sintering additive onto the carrier by grinding calcium fluoride and magnesium fluoride with the aluminium oxide carrier and firing the mixture at a temperature above 940 o C.
  • aluminium oxide as carrier achieves two objects on the one hand the eutectic additive gets caked to a smaller extent during the preparation thereof, while on the other hand required quantity thereof can be weighed in more precisely and accurately in this "diluted" form.
  • the eutectic sintering additive used according to the process of the present invention can be particularly preferably prepared by using 55.6 % by weight of calcium fluoride and 44.4 % by weight of magnesium fluoride. It is preferred to add 0.8 % by weight of the eutectic sintering additive to the aluminium oxide starting material.
  • the process of the present invention can be carried out in conventional and known equipment generally used in the manufacture of sintered aluminium oxide ceramics and no special apparatus is required. All the starting materials used are readily available.
  • the finely ground powder used can be worked up by any known forming procedure and the sintering process can be accomplished in any generally used gas or electrically fired chamber- or tunnel-furnace in oxidizing atmosphere.
  • the process of the present invention can be accomplished at a lower temperature than the known methods while at the same time the products thus obtained show increased abrasion resistance and are superior to ceramics of similar destination obtained by known methods.
  • Example 1 556 g of technical grade calcium fluoride and 444 g of technical grade magnesium fluoride are weighed in a grinding mill comprising alumina balls.
  • the powder mixture is preferably subjected to dry homogenizing grinding; the average particle size amounts to 1-2 ⁇ m (90 %).
  • the ground powder is compacted in a manner known per se (e.g. by granulating and pressing), whereupon the shaped articles thus obtained are subjected to thermal treatment in a heating sheath (on the air) in an oxidizing atmosphere, at first at 1150-1170 o C for an hour and thereafter at 940-970 ° C for 2 hours.
  • the cooled product - at least 90 % thereof being characterized by the formula CaF 2 .MgF 2 - is powdered and ground again; about 80-90 % of the powder has a particle size below 10 ⁇ m.
  • the eutectic sintering additive No. 1 thus obtained is used as follows:
  • From the powder mixture balls are formed by die-cast in a manner known per se by melting with 14 % by weight of paraffine, embedding into alumina, removing the paraffine and sintering.
  • the said procedure is carried out at a heating rate of 120-150 ° C/hour at 1300 ° C for 4 hours, then increasing the temperature to 1550 o C, heating at this temperature for a further period of 8 hours in an oxidizing (air) atmosphere.
  • the nominal aluminium oxide content of shaped articles thus prepared amounts to 99.1 % by weight (calculated on the basis of the weighing-in), the magnesium oxide content is 0.1 % by weight (in Spinel form) at a maximum CaF 2 .MgF 2 content of 0.8 % by weight.
  • gypsum cylindrical plaster of Paris
  • the nominal aluminium oxide content of the shaped articles thus prepared by slip-casting forming amounts to 98.9 % by weight; magnesium oxide content: 0.1 % by weight; chrome oxide content: 0.2 % by weight; at a maximum CaF 2 MgF 2 content of 0.8 % by weight.
  • Example 3 Into a ball mill 385 g of technical or analytical grade calcium fluoride and 615 g of technical or analytical grade magnesium fluoride are weighed in, whereupon the powder mixture is subjected to homogenizing grinding to yield an average particle size of 1-2 ⁇ m (90 %). After compacting the shaped articles are ignited by thermal treatment at first at 1180-1200 o C for an hour and subsequently at 960-1000 ° C for 2 hours.
  • the cooled product - at least 95 % thereof being characterized by the formula CaF 2 .2MgF 2 - is pulverized and finely ground to yield a particle size below 10/um (80- 90 % ) .
  • the product thus obtained as eutectic sintering additive No. 2 is used as follows.
  • a grinding mill comprising alumina balls 991.5 g of aluminium oxide of high purity calcinated at 1500 o C are weighed in, whereupon 2 g of sintering additive No. 2, 3.5 g of magnesium spinel and 2 g of analytical grade eerie oxide are added.
  • the powder mixture is ground preferably in dry medium to an average particle size of 5 ⁇ m (95 % ) including 50 % of a particle size below 1 ⁇ m.
  • the powder is formed in a known manner by isostatic pressing under a.
  • the nominal aluminium oxide content of the shaped articles thus obtained by "three-dimension" pressing amounts to 99.4 % by weight, the magnesium oxide content is 0.1 % by weight, the eerie oxide content amounts to 0.2 % by weight, at a maximal CaF 2 .2MgF 2 content of 0.2 % by weight.
  • Example 4 715 g of technical grade calcium fluoride, 285 g of technical grade magnesium fluoride and 1000 g of aluminium oxide calcinated at a temperature not exceeding 1300 o C /having a total alkali content below 0.1 %, specific surface more than 5 m 2 /g (BET)/ are weighed in.
  • the powder mixture is ground at a rate that 90 % of the particles have an average particle size of 5/Um including 50 % below
  • the powder is compacted it shaped articles, which are subjected to thermal treatment at first at 1200-1250 o C for an hour and thereafter at 1050-110 ° C for 3 hours.
  • the caked powder mixture thus obtained is finely ground at a rate that 80-90 % of the particles should be below
  • the eutectic sintering additive No. 3 thus obtained can be characterized by the formula 2CaP 2 .MgF 2 and is applied onto an aluminium oxide carrier at a "dilution" rate of 1:1.
  • the product is used as follows:
  • the powder mixture is subjected to homogenizing stirring whereupon it is admixed with 3 % by weight of polyiso ⁇ butylene pressing additive (described in Hungarian patent No. 165,357), granulated and formed to shaped articles under a Dressure of at least 0.1 MPa.
  • polyiso ⁇ butylene pressing additive described in Hungarian patent No. 165,357
  • Sintering is carried out in air at a heatins rate of 130-150 ° C/hour, at 1300 ° C for 2 hours, at 1550 ° C for 8 hours.
  • the nominal total aluminium oxide content of the ceramics thus obtained amounts to 96 % by weight at a maximum 2CaF 2 .MgF 2 content of 4 % by weight.
  • Apparent density 3.80 g/cm 3 ; water absorption: 0.5 % by weight; surface: rough.
  • Example 5 967 g of alumina (type "G") are weighed in a mill comprising alumina balls, whereupon 20 g of sintering additive No. 2, 10 g of technical grade zirconium silicate and 3 g of technical grade nickel oxide are added.
  • the powder mixture is subjected to grinding in aqueous medium in the presence of an antifoam agent at a rate that 90 % of the articles should have an average particle size below 5 ⁇ m and 50 % thereof being 1-2 ⁇ m. From the mass thus obtained thick-wall pipes are formed by eentrifuging slip-casting or compact bars are casted.
  • the product is dried and sintered under oxidizing conditions.
  • the heating rate of 80-100 ° C/hour, at 1200 ° C for an hour, at 1300 ° C for 4 hours and finally at 1550 ° C for 6 hours.
  • the nominal aluminium oxide content of the shaped articles thus obtained amounts to 96.7 % by weight
  • the zirconium silicate content is 1 % by weight
  • the nickel oxide content amounts to 0.3 % by weight
  • Example 6 781 g of alumina post-calcinated at 1500 ° C, type "G" (Hungarian patent No. 179,981) are weighed in a grinding mill, whereupon 200 g of alkali-free gamma-aluminium oxide calcinated at 900-1100 ° C, 5 g of sintering additive No.2, 10 g of technical grade zirconium oxide, 3 g of technical grade eerie oxide (for the stabilization of the pre vious component) and 1 g of magnesium oxide are added.
  • the powder mixture is ground to the particle size disclosed above and extruded in a known manner for bored tubes by using a polyvinyl alcohol binder and plasticizer.
  • the tubes are dried and sintered - preferably in suspended form - in an oxidizing atmosphere, at a heating rate of 100-120 ° C, at 1350 ° C for 3 hours, at 1400 ° C for 5 hours and finally at 1550 ° C for 8 hours.
  • the nominal aluminium oxide content of the shaped articles thus prepared amounts to 58.1 % by weight, the zirconium oxide content is 1 % by weight, the ceric oxide content amounts to 0.3 % by weight, the magnesium oxide content is 0.1 % by weight, at a maximum CaF 2 .2MgF 2 content of 0.5 70 by weight.
  • Linear shrinkage 17 %.
  • sintering additive No. 3 2 g of chrome oxide
  • 15 g of industrial grade calcium feldspar /CaO .20.1 % by weight
  • Al 2 O 3 3
  • the nominal aluminium oxide content of the sintered articles amounts to 97.4 % by weight, the chrome oxide content is 0.2 % by weight, the calcium feldspar content amounts to 1.5 % by weight (in the form of glass phase), the magnesium oxide content amounts to 0.1 % by weight, at a maximum 2CaF 2 .MgF 2 content of 0.8 % by weight.
  • Example 8 Alumina hydrate (type K-33; made free of alkaline; manufacturer: Almasfuzitoi Timfbldgyar) calcinated at 1500 o C for 3 hours, whereupon 973 g of the calcinated product are weighed in a grinding mill, 1 g of sintering additive No. 1, 10 g of chrome oxide, 6 g of zirconium silicate and 10 g of magnesium spinel are added.
  • the powder mixture is ground preferably in aqueous medium in an analoguous manner to the particle size described in the previous Examples, whereupon it is formed to thick-wall tubes, rings and discs by slip-casting.
  • the shaped articles are dried and sintered in an oxidizing atmosphere, at a heating rate of 120-130 ° C/hour, at first at 1500 ° C for 6 hours and then at 1600 o C for 8 hours.
  • the shaped articles are allowed to cool in the furnace depending on the size, wall-thickness and weight of the shaped articles.
  • the nominal aluminium oxide content of the sintered aluminium oxide ceramics amounts to 98 % by weight, the chrome oxide content is 1 % by weight, the zirconium silicate content is 0.6 % by weight, the magnesium oxide content amounts to 0.3 % by weight, at a maximum CaF 2 .MgF 2 content of 0.1 % by weight.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Compositions Of Oxide Ceramics (AREA)
PCT/HU1987/000009 1987-03-05 1987-03-05 Process for the preparation of aluminium oxide ceramics having increased abrasion resistance Ceased WO1988006575A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
AT904187A AT393120B (de) 1987-03-05 1987-03-05 Verfahren zur herstellung von aluminiumoxidkeramik, die eine erhoehte abriebsfestigkeit hat
DE19873790916 DE3790916T1 (de) 1987-03-05 1987-03-05 Verfahren zur herstellung von aluminiumkeramik, die eine erhoehte abriebsfestigkeit hat
PCT/HU1987/000009 WO1988006575A1 (en) 1987-03-05 1987-03-05 Process for the preparation of aluminium oxide ceramics having increased abrasion resistance
NL8720112A NL8720112A (nl) 1987-03-05 1987-03-05 Werkwijze voor de bereiding van aluminiumoxide keramische materialen met verhoogde slijtvastheid.
CH421788A CH677110A5 (https=) 1987-03-05 1987-03-05
JP87501685A JPH01502426A (ja) 1987-03-05 1987-03-05 耐摩耗性の増加した酸化アルミニウムセラミックスの調製方法
GB8826043A GB2209334B (en) 1987-03-05 1988-11-07 Process for the preparation of aluminium oxide ceramics having increased abrasion resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/HU1987/000009 WO1988006575A1 (en) 1987-03-05 1987-03-05 Process for the preparation of aluminium oxide ceramics having increased abrasion resistance

Publications (1)

Publication Number Publication Date
WO1988006575A1 true WO1988006575A1 (en) 1988-09-07

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PCT/HU1987/000009 Ceased WO1988006575A1 (en) 1987-03-05 1987-03-05 Process for the preparation of aluminium oxide ceramics having increased abrasion resistance

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JP (1) JPH01502426A (https=)
AT (1) AT393120B (https=)
CH (1) CH677110A5 (https=)
DE (1) DE3790916T1 (https=)
GB (1) GB2209334B (https=)
NL (1) NL8720112A (https=)
WO (1) WO1988006575A1 (https=)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007029237A3 (en) * 2005-09-08 2007-07-05 Imi Tami Institute Research Improved alumina based ceramic objects
WO2011012125A1 (de) * 2009-07-30 2011-02-03 Fraunhofer Gesellschaft Zur Förderung Der Angewandten Forschung E. V. α-Al2O3-SINTERMATERIAL UND VERFAHREN ZUR HERSTELLUNG EINES HOCHDICHTEN UND FEINSTKRISTALLINEN FORMKÖRPERS AUS DIESEM MATERIAL SOWIE DEREN VERWENDUNG

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6083451A (en) * 1995-04-18 2000-07-04 Applied Materials, Inc. Method of producing a polycrystalline alumina ceramic which is resistant to a fluorine-comprising plasma
US6247519B1 (en) * 1999-07-19 2001-06-19 Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of Natural Resources Preform for magnesium metal matrix composites
RU2168483C1 (ru) * 2000-03-07 2001-06-10 Институт химии Коми научного центра Уральского отделения РАН Шихта для получения конструкционной глиноземистой керамики и способ изготовления изделий из нее
JPWO2023033066A1 (https=) * 2021-08-31 2023-03-09

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54102312A (en) * 1978-01-31 1979-08-11 Hitachi Ltd Alumina base porcelain composition
CS193669B1 (en) * 1974-07-23 1979-11-30 Stanislav Chylek Method for producing ceramic material based on alumina and objects from the said material
US4292049A (en) * 1979-05-25 1981-09-29 Ngk Spark Plug Co., Ltd. Ceramic materials for high-speed cutting
JPS59156961A (ja) * 1983-02-24 1984-09-06 松下電器産業株式会社 アルミナ焼結基板の製造方法

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CS193669B1 (en) * 1974-07-23 1979-11-30 Stanislav Chylek Method for producing ceramic material based on alumina and objects from the said material
JPS54102312A (en) * 1978-01-31 1979-08-11 Hitachi Ltd Alumina base porcelain composition
US4292049A (en) * 1979-05-25 1981-09-29 Ngk Spark Plug Co., Ltd. Ceramic materials for high-speed cutting
JPS59156961A (ja) * 1983-02-24 1984-09-06 松下電器産業株式会社 アルミナ焼結基板の製造方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
V.A. KIREEV, "Kurs Fizicheskoi Khimii", 1955, GKHI, (Moscow), p. 408. *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007029237A3 (en) * 2005-09-08 2007-07-05 Imi Tami Institute Research Improved alumina based ceramic objects
WO2011012125A1 (de) * 2009-07-30 2011-02-03 Fraunhofer Gesellschaft Zur Förderung Der Angewandten Forschung E. V. α-Al2O3-SINTERMATERIAL UND VERFAHREN ZUR HERSTELLUNG EINES HOCHDICHTEN UND FEINSTKRISTALLINEN FORMKÖRPERS AUS DIESEM MATERIAL SOWIE DEREN VERWENDUNG

Also Published As

Publication number Publication date
GB2209334B (en) 1991-10-16
GB2209334A (en) 1989-05-10
CH677110A5 (https=) 1991-04-15
JPH01502426A (ja) 1989-08-24
DE3790916T1 (de) 1989-05-03
ATA904187A (de) 1991-01-15
AT393120B (de) 1991-08-26
NL8720112A (nl) 1989-02-01

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