[go: up one dir, main page]

CN100509692C - Tungsten corundum ceramic material and low temperature sintering method - Google Patents

Tungsten corundum ceramic material and low temperature sintering method Download PDF

Info

Publication number
CN100509692C
CN100509692C CNB200710147095XA CN200710147095A CN100509692C CN 100509692 C CN100509692 C CN 100509692C CN B200710147095X A CNB200710147095X A CN B200710147095XA CN 200710147095 A CN200710147095 A CN 200710147095A CN 100509692 C CN100509692 C CN 100509692C
Authority
CN
China
Prior art keywords
tungsten
sintering
corundum ceramic
ceramic material
hours
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.)
Expired - Fee Related
Application number
CNB200710147095XA
Other languages
Chinese (zh)
Other versions
CN101148352A (en
Inventor
杨淑金
吴伯麟
张楠
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.)
Guilin University of Technology
Original Assignee
Guilin University of Technology
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 Guilin University of Technology filed Critical Guilin University of Technology
Priority to CNB200710147095XA priority Critical patent/CN100509692C/en
Publication of CN101148352A publication Critical patent/CN101148352A/en
Application granted granted Critical
Publication of CN100509692C publication Critical patent/CN100509692C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Compositions Of Oxide Ceramics (AREA)

Abstract

本发明公开了一种钨刚玉陶瓷材料及低温烧结方法。钨刚玉陶瓷材料中原料重量百分比含量为:氧化铝粉85~99.5%、氧化钨0.1~3.0%、粘土0.1~14.5%、长石0.1~14.5%、碳酸钙0.1~14.5%、滑石0.1~14.5%。步骤为:将上述原料球磨混合3小时后在空气中于100℃烘干24小时;采用冷等静压成型,在200~300MPa下保压3分钟;在硅钼炉中1350~1550℃保温0.5~3小时烧结,随炉冷却,可获得钨刚玉陶瓷材料。本发明采用一般工业设备,工艺简单,有利于刚玉陶瓷工业化生产;不仅显著降低氧化铝陶瓷的烧结温度,同时抗弯强度可以达到350~600Mpa;能显著降低高铝陶瓷生产中的高温能耗及产品成本,同时获得高强氧化铝陶瓷。

Figure 200710147095

The invention discloses a tungsten corundum ceramic material and a low-temperature sintering method. The weight percentage content of raw materials in tungsten corundum ceramic materials is: alumina powder 85-99.5%, tungsten oxide 0.1-3.0%, clay 0.1-14.5%, feldspar 0.1-14.5%, calcium carbonate 0.1-14.5%, talc 0.1-14.5% %. The steps are: mix the above raw materials by ball milling for 3 hours, and then dry them in the air at 100°C for 24 hours; use cold isostatic pressing, and hold the pressure at 200-300MPa for 3 minutes; After ~3 hours of sintering and cooling with the furnace, tungsten corundum ceramic materials can be obtained. The present invention adopts general industrial equipment, and the process is simple, which is beneficial to the industrial production of corundum ceramics; not only significantly reduces the sintering temperature of alumina ceramics, but also can achieve a bending strength of 350-600Mpa; it can significantly reduce high-temperature energy consumption and Product cost, while obtaining high-strength alumina ceramics.

Figure 200710147095

Description

A kind of tungsten corundum ceramic material and low-temperature sintering method
Technical field
The invention belongs to the alumina ceramic material technical field, particularly a kind of corundum ceramic material and low-temperature sintering method thereof that adds Tungsten oxide 99.999.
Background technology
Alumina-ceramic claims the corundum porcelain again, has excellent mechanical property, electrical property, thermal characteristics, very high specular reflectance excluded, erosion resistance, abundant raw material is inexpensive and than MgO, SiC, Si 3N 4Pottery is the characteristic of easy-sintering more, it is the base mateiral that is used for making multiple high strength, performance ceramic component such as wear-resistant, high temperature resistant, and demand is huge, thereby concern extremely both domestic and external, in modern industry and modern science and technology field, obtain application more and more widely, be present most widely used a kind of special cermacis, Application Areas relates to every field such as metallurgy, chemical industry, electromechanics, boats and ships, aerospace, military affairs.In alumina-ceramic is produced, all exist same problem both at home and abroad, promptly can not make the high-performance alumina-ceramic with existing industrial production technology, low cost.The sintering temperature of alumina ceramics is up to 1600~1700 ℃, and investment is big, the energy consumption height, and bending strength generally only is 250-350MPa.Quality product is difficult to further improve, and has limited applying of it.The alumina-ceramic sintering temperature is higher, easily causes grain growth, causes mechanical properties decrease generally to adopt the way that adds the liquid phase substance acceleration of sintering.By the difference of the mode of action, additive is by the sintering of two kinds of form promotes oxidn aluminium.The first, form liquid phase between additive system itself or additive and the alumina substrate, this class additive such as SiO 2And MgO, CaO, SrO, BaO etc., the existence of liquid phase has made things convenient for the rearrangement of alumina particle, simultaneously by melting-the PRECIPITATION MECHANISM acceleration of sintering.The second, form sosoloid with alumina substrate,, make rate of diffusion become big by increasing the lattice distortion of aluminum oxide, thus acceleration of sintering.Additive such as TiO 2, Cr 2O 3, Fe 2O 3, MnO 2, Y 2O 3Deng.But, when add-on more after a little while, sintering temperature is still higher; When add-on increased, though help sintering, descending by a relatively large margin appearred in final material mechanical performance.
In order to address these problems, Chinese scholars had all been carried out number of research projects in recent years.Both at home and abroad impressive progress has been obtained about the research level of alumina-ceramic in the laboratory, and Japanese scientist develops bending strength in the nineties and reaches〉alumina sample of 1000MPa.Proposition is made raw material with superfine alumina powder, can prepare the excellent dense base substrate at 1400 ℃ of sintering, but its superfine alumina powder complicated process of preparation, cost is very high.There is similar problem at present equally in China, though domestic scholars is also being done number of research projects aspect the sintering temperature of alumina raw material preparation and reduction alumina-ceramic, all fundamentally do not solve the price of alumina-ceramic and the contradiction between the performance, the researchist of China also obtains bending strength 300~500MPa under laboratory condition, even the alumina sample of 1000MPa, the raw material that adopts is that superfine nano aluminum oxide powder and nanometer silicon carbide compound material add spark plasma sintering or HIP sintering, its bending strength is greatly improved, but do not have industrial value, industrial production can't be promoted.
Summary of the invention
The objective of the invention is is exactly to adopt industrial raw material, by adding Tungsten oxide 99.999, utilize the atmospheric low-temperature sintering technology to prepare the high-strength alumina pottery of the big 300~600MPa of bending strength, can solve above-mentioned sintering temperature too high, adopt ultrafine powder or excessive, the problem that product cost is high with ionic discharge sintering or energy consumption that HIP sintering produced.
The raw material weight percent content is in the tungsten corundum ceramic material that the present invention relates to: aluminum oxide powder 85~99.5%, Tungsten oxide 99.999 0.1~3.0%, clay 0.1~14.5%, feldspar 0.1~14.5%, lime carbonate 0.1~14.5%, talcum 0.1~14.5%.
Concrete steps are:
(1) in aluminum oxide powder, add Tungsten oxide 99.999, with clay, feldspar, lime carbonate, talcum as sintering aid;
(2) mixing of above-mentioned raw materials ball milling was dried 24 hours in 100 ℃ in air after 3 hours;
(3) 3 minutes cold isostatic compactions of pressurize under 200~300MPa;
(4) 0.5~3 hour sintering of 1350~1550 ℃ of insulations in silicon molybdenum stove, furnace cooling, can obtain bending strength is that 300~600MPa sintered compact is a tungsten corundum ceramic material.
The present invention adopts general industry equipment, and technology is simple, helps the corundum ceramic suitability for industrialized production; Not only significantly reduce the sintering temperature of alumina-ceramic, bending strength can reach 350~600Mpa simultaneously; Can significantly reduce high temperature energy consumption and product cost in the high alumina ceramic production, obtain the high-strength alumina pottery simultaneously.
Description of drawings
Fig. 1 is a process flow sheet of the present invention.
Embodiment
Embodiment 1:
(1) raw material weight per-cent is: α-Al 2O 3Powder 90%, Tungsten oxide 99.999 1%, feldspar 3%, lime carbonate 2%, clay 3% and talcum 1%, batching according to the above ratio;
(2) mixing of above-mentioned raw materials ball milling was dried 24 hours in 100 ℃ in air after 3 hours;
(3) adopt cold isostatic compaction, pressurize is 3 minutes under 200MPa;
(4) in silicon molybdenum stove under 1430 ℃ of normal pressures sintering, be incubated 2 hours.
The bending strength of obtained product is 450MPa.
Embodiment 2:
(1) raw material weight per-cent is: α-Al 2O 3Powder 95%, Tungsten oxide 99.999 2%, feldspar 0.5%, lime carbonate 1%, clay 1% and talcum 0.5%, batching according to the above ratio;
(2) mixing of above-mentioned raw materials ball milling was dried 24 hours in 100 ℃ in air after 3 hours;
(3) adopt cold isostatic compaction, pressurize is 3 minutes under 300MPa;
(4) in silicon molybdenum stove under 1520 ℃ of normal pressures sintering, be incubated 2 hours.
The bending strength of obtained product is 550MPa.

Claims (2)

1. a tungsten corundum ceramic material is characterized in that the raw material weight degree of tungsten corundum ceramic material is: aluminum oxide powder 85~99.5%, Tungsten oxide 99.999 0.1~3.0%, clay 0.1~14.5%, feldspar 0.1~14.5%, lime carbonate 0.1~14.5%, talcum 0.1~14.5%.
2. the low-temperature sintering method of the described tungsten corundum ceramic material of claim 1 is characterized in that concrete steps are:
(1) in aluminum oxide powder, add Tungsten oxide 99.999, with clay, feldspar, lime carbonate, talcum as sintering aid;
(2) mixing of above-mentioned raw materials ball milling was dried 24 hours in 100 ℃ in air after 3 hours;
(3) adopt cold isostatic compaction, pressurize is 3 minutes under 200~300MPa pressure;
(4) 0.5~3 hour sintering of 1350~1550 ℃ of insulations in silicon molybdenum stove, furnace cooling, can obtain bending strength is that 300~600MPa sintered compact is a tungsten corundum ceramic material.
CNB200710147095XA 2007-09-04 2007-09-04 Tungsten corundum ceramic material and low temperature sintering method Expired - Fee Related CN100509692C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB200710147095XA CN100509692C (en) 2007-09-04 2007-09-04 Tungsten corundum ceramic material and low temperature sintering method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB200710147095XA CN100509692C (en) 2007-09-04 2007-09-04 Tungsten corundum ceramic material and low temperature sintering method

Publications (2)

Publication Number Publication Date
CN101148352A CN101148352A (en) 2008-03-26
CN100509692C true CN100509692C (en) 2009-07-08

Family

ID=39249066

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB200710147095XA Expired - Fee Related CN100509692C (en) 2007-09-04 2007-09-04 Tungsten corundum ceramic material and low temperature sintering method

Country Status (1)

Country Link
CN (1) CN100509692C (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101412619B (en) * 2008-11-12 2013-04-17 李海峰 Micropore hydrogenated aluminum porcelain tube and preparation thereof
KR101903355B1 (en) * 2012-01-11 2018-11-22 생-고뱅 세라믹스 앤드 플라스틱스, 인코포레이티드 Refractory object and process of forming a glass sheet using the refractory object
KR102363114B1 (en) * 2017-12-27 2022-02-15 쇼와 덴코 가부시키가이샤 Alumina sintered body precursor, alumina sintered body manufacturing method, grinding stone particle manufacturing method and alumina sintered body
CN110903076B (en) * 2019-12-03 2020-12-25 浙江科奥陶业有限公司 Corundum refractory product for hydrogen-filled molybdenum rod heating furnace and application method thereof
CN111747734A (en) * 2020-05-22 2020-10-09 广东日禾电器有限公司 Preparation method of low-temperature sintering heating ceramic material

Also Published As

Publication number Publication date
CN101148352A (en) 2008-03-26

Similar Documents

Publication Publication Date Title
CN102746013B (en) Light high-strength silicon nitride and silicon carbide combined refractory material and preparation method thereof
CN101182193B (en) A kind of preparation method of in-situ self-toughened alumina ceramics
CN111620679B (en) Method for preparing high-purity mullite material by taking fused silica as silicon source
CN104045350B (en) Method for preparing silicon nitride /silicon carbide ceramic composite by use of reaction sintering process
CN106904950A (en) A kind of low sintering 95 alumina ceramic material
CN103755332B (en) Desert wind sand is utilized to prepare the method for cordierite ceramic
CN105174905A (en) Light thermal insulation ceramic product and preparation method thereof
CN100509692C (en) Tungsten corundum ceramic material and low temperature sintering method
CN103833383B (en) A kind of preparation method of corundum-magnesium-aluminium spinel matter refractory aggregate of unicellular structure
CN1264777C (en) Reinforced daily ceramic manufacturing process
CN106380176A (en) High-plasticity daily heat-resistant ceramic and preparation method thereof
CN100532319C (en) A kind of molybdenum corundum ceramic material and low-temperature sintering method
CN113336563A (en) Sialon whisker-corundum composite ceramic material using natural mineral as raw material, preparation method thereof and prepared product
CN101734925A (en) Silicon nitride porous ceramics with controllable porosity and preparation method thereof
CN101514750A (en) Nano-carbon fiber complex silicon carbide ceramics ring and preparation method thereof
CN101734920A (en) Titanium nitride porous ceramics and preparation method thereof
CN115043648A (en) Prestressed alumina ceramic composite material and preparation method thereof
CN108017397A (en) Refractory brick containing quartz sand and preparation method thereof
CN108285350B (en) A kind of ternary composite silicon carbide refractory material and preparation method thereof
CN102181766B (en) A kind of (Ti, Cr) 2AlC solid solution composite material and its preparation method
CN101538150A (en) Ceramics of improving mechanical strength and cold and hot shock property and preparation method thereof
CN109081687A (en) A kind of highly heatproof and shockproof ceramic crucible and preparation method thereof suitable for calcining anode material of lithium battery
CN111205674B (en) Ceramic pigment composition, yellow glass ceramic pigment, glass ceramic and preparation method thereof
CN104291825B (en) A kind of to synthesize the SiC ceramic low-temperature melt producing method that celsian-felspar is sintering aid
CN115321946A (en) Long-life low-cost refractory castable and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20090708

Termination date: 20180904