CN1114642A - Method for producing high-purity micro-crystal white alundum - Google Patents
Method for producing high-purity micro-crystal white alundum Download PDFInfo
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- CN1114642A CN1114642A CN 94108417 CN94108417A CN1114642A CN 1114642 A CN1114642 A CN 1114642A CN 94108417 CN94108417 CN 94108417 CN 94108417 A CN94108417 A CN 94108417A CN 1114642 A CN1114642 A CN 1114642A
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- al2o3
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- mix
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Abstract
The present invention provides a production method of high-purity micro-crystal white alundum. Its method is as follows: H3PO4 and gamma Al2O3 are uniformly mixed, and then calcined so as to convert gamma Al2O3 to alpha Al2O3, and then HF is used, and water-grinding balls are added and uniformly mixed with the alpha Al2O3, and water-ground, and then the water-ground alpha Al2O3 is dried, and then an organic binding agent is mixed uniformly with the dried alpha Al2O3, and then the above-mentioned materials are passed through such processes of forming, drying and calcining at high-temp., natural cooling, so that the invented product can be obtained. Said product is refractory, stable in chemical and physical properties, and its micro-crystal complex is small, so that it is favourable for practical application.
Description
The present invention relates to a kind of production method of high-purity micro-crystal white alundum, belong to alumina high temperature stupalith field.
At present, in the alumina high temperature ceramic material of selling, according to Inst. of Geochemistry, Chinese Academy of Sciences the tabular white fused alumina of japanese product is carried out the random sampling chemical examination on market, its result is:
Chemical analysis: Al
2O
397%
Na
2O+K
2O 0.32%
SiO
2 0.25%
CaO+MgO 0.25%
γ Al
2O
3Remaining phase 1.5%
Physical property: volume density 3.65g/cm
3
Crystalline phase 20 μ μ crystallite aggregates are wherein because Na
2O+K
2O, SiO
2And γ Al
2O
3(gamma aluminium oxide) remaining height of comparing, so the resistance to elevated temperatures of its product is just not so good with chemistry, physical stability, because its crystallite aggregate is also bigger than normal, this will be unfavorable for use in addition.
Purpose of the present invention just provides a kind of Na of containing
2O, K
2O, SiO
2And γ Al
2O
3The production method of the high-purity micro-crystal white alundum low, that the crystallite aggregate is little.
The present invention is achieved in that it comprises H
3PO
4(phosphoric acid), γ Al
2O
3, HF (hydrofluoric acid), will account for γ Al
2O
3The H of gross weight 1%~5%
3PO
4With γ Al
2O
3Mix, 1200 ℃~1600 ℃ temperature lower calcinations 2~6 hours, so just obliterated part Na
2O, K
2O, CaO, MgO and Fe
2O
3, make γ Al
2O
3Convert α Al to
2O
3, and guarantee α Al
2O
3Content reach 80%, be that 1%~5% HF adds water mill ball and α Al with concentration
2O
3Mix and carried out water mill 32~40 hours, to remove SiO
2With raising density, then with the α Al behind the water mill
2O
3Carrying out drying, is 1 ‰~4 ‰ organic bond and dried α Al with concentration
2O
3Mix, afterwards reshaping, drying, and naturally lower the temperature to come out of the stove after 3~7 hours at 1600 ℃~1800 ℃ temperature lower calcination and get final product.
Owing to adopted aforementioned production method, the performance of its product is as follows:
Chemical analysis: Al
2O
399.5%
Na
2O+K
2O <0.032%
SiO
2 <0.2%
CaO+MgO <0.02%
γ Al
2O
3Remaining phase<1%
Physical property: volume density 〉=3.7g/cm
3
Crystalline phase<5 μ μ crystallite aggregates
From on can find out the present invention compared with prior art, its Na
2O, K
2O, SiO
2And γ Al
2O
3Low, the crystallite aggregate is little, so the resistance to elevated temperatures of its product and chemistry, physical stability is all good than prior art, because its crystallite aggregate is little, this is conducive to actual use very much in addition.
Further specify embodiments of the invention below:
In the present embodiment: will account for γ Al
2O
3The H of gross weight 2%
3PO
4With γ Al
2O
3Mixing, 1450 ℃ of temperature lower calcinations 4 hours, is that 3% HF adds water mill ball and α Al with concentration
2O
3Mix and carried out water mill 36 hours, then with the α Al behind the water mill
2O
3Carrying out drying, is 2 ‰ organic bond and dried α Al with concentration
2O
3Mix, afterwards again balling-up in pan-pelletizer, then dry, and naturally lower the temperature to come out of the stove after 5 hours at 1750 ℃ temperature lower calcination and get final product.
Claims (1)
1, a kind of production method of high-purity micro-crystal white alundum, it comprises H
3PO
4, γ Al
2O
3, HF, it is characterized in that: will account for γ Al
2O
3The H of gross weight 1%~5%
3PO
4With γ Al
2O
3Mix, 1200 ℃~1600 ℃ temperature lower calcinations 2~6 hours, make γ Al
2O
3Convert α Al to
2O
3, be that 1%~5% HF adds water mill ball and α Al with concentration
2O
3Mix and carried out water mill 32~40 hours, then with the α Al behind the water mill
2O
3Carrying out drying, is 1 ‰~4 ‰ organic bond and dried α Al with concentration
2O
3Mix, afterwards reshaping, drying, and naturally lower the temperature to come out of the stove after 3~7 hours at 1300 ℃~1800 ℃ temperature lower calcination and get final product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 94108417 CN1114642A (en) | 1994-07-08 | 1994-07-08 | Method for producing high-purity micro-crystal white alundum |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 94108417 CN1114642A (en) | 1994-07-08 | 1994-07-08 | Method for producing high-purity micro-crystal white alundum |
Publications (1)
Publication Number | Publication Date |
---|---|
CN1114642A true CN1114642A (en) | 1996-01-10 |
Family
ID=5033462
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 94108417 Pending CN1114642A (en) | 1994-07-08 | 1994-07-08 | Method for producing high-purity micro-crystal white alundum |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1114642A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1125791C (en) * | 1998-05-18 | 2003-10-29 | 武汉工业大学 | Fine alumina ceramic preparation process using natural bauxite |
CN104499051A (en) * | 2014-12-05 | 2015-04-08 | 三祥新材股份有限公司 | Single crystal corundum production method |
-
1994
- 1994-07-08 CN CN 94108417 patent/CN1114642A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1125791C (en) * | 1998-05-18 | 2003-10-29 | 武汉工业大学 | Fine alumina ceramic preparation process using natural bauxite |
CN104499051A (en) * | 2014-12-05 | 2015-04-08 | 三祥新材股份有限公司 | Single crystal corundum production method |
CN104499051B (en) * | 2014-12-05 | 2017-05-10 | 三祥新材股份有限公司 | Single crystal corundum production method |
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