CN1800024A - Plate-like aluminum oxide granule preparation method - Google Patents

Plate-like aluminum oxide granule preparation method Download PDF

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CN1800024A
CN1800024A CN 200610023323 CN200610023323A CN1800024A CN 1800024 A CN1800024 A CN 1800024A CN 200610023323 CN200610023323 CN 200610023323 CN 200610023323 A CN200610023323 A CN 200610023323A CN 1800024 A CN1800024 A CN 1800024A
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tabular
salt
particle
fused
decomposed
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CN100378002C (en
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高濂
靳喜海
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Shanghai Institute of Ceramics of CAS
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Shanghai Institute of Ceramics of CAS
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Abstract

The invention discloses a plate-shaped Al2O3 particle making method and dimension control method in the fine chemical domain, which comprises the following steps: taking partial decomposed aluminum salt as Al2O3 pioneer body; making the Al2O3 particle through fused salt method; controlling the particle dimension precisely through adding plate-shaped Al2O3 seed in the raw material powder; making the dimension of Al2O3 particle between sub-micron and several micron.

Description

The preparation method of plate-like aluminum oxide granule
Technical field
The present invention relates to a kind of plate-like aluminum oxide (Al2O 3) preparation method of particle, relate to or rather a kind of tabular Al2O 3The preparation of particle and the method for size Control thereof belong to field of fine chemical.
Background technology
Tabular Al2O 3Particle is a kind of important raw material of industry. Tabular Al in complex phase ceramic2O 3Can increase substantially crack deflection and bridging effect in the porcelain body as a kind of flexibilizer, improve the toughness of material. Utilize tabular Al2O 3High-termal conductivity, in the plastic electronic encapsulating material, introduce tabular Al2O 3Can increase substantially the thermal conductivity of plastics, improve the radiating effect of electronic device. In addition, tabular Al2O 3Particle is still by the standby texturing Al of template-mediated grain growth legal system2O 3The template particles that pottery is indispensable. Studies show that recently some texturing Al2O 3The comprehensive mechanical property of pottery is far above common Al2O 3Pottery, its intensity can reach about 800MPa, and its toughness reaches 10-11 MPam1/2 At present about tabular Al2O 3The preparation method of particle mainly contains the auxiliary mass transferring in gas phase Al of AlF2O 3Plate-like particles growth method and [the Richard F.Hill such as molten-salt growth method take al inorganic salt as raw material, Robert Danzer and Robert T.Paine.Synthesis of Alumina Oxide Platelets, J.Am.Ceram.Soc. 84 (3) 514-20,2001, S.Hashimoto, and A.Yamaguchi.Synthesis of α-Al2O 3Platelets Using Sodium Sulfate Flux, J.Mater.Res., 14 (12) 4667-72,1999]. But from existing report, the tabular Al of gained2O 3The size of particle is thicker (5~33 μ m) generally, and is not only inhomogeneous, and agglomeration is often more serious. This is unfavorable for the subsequent applications of material. In addition, still there is not a kind of feasible method to the tabular Al of gained at present2O 3Particle size is accurately controlled.
Summary of the invention
The object of the present invention is to provide a kind of tabular Al2O 3The preparation method of particle is to overcome current tabular Al2O 3The problems referred to above that exist in the preparation of particle.
The enforcement of the object of the invention be the aluminium salt that decomposes be that raw material has prepared size evenly by molten-salt growth method and approximately has been the tabular Al that monodisperse status distributes2O 3Particle, and by tabular Al in the control preparation process2O 3The addition of crystal seed has been realized Al in the end product2O 3The accurate control of plate-like particles size. This is to tabular Al2O 3Production and the application of powder have great importance.
Specifically, at first aluminium salt is calcined under proper temperature and made it the part thermal decomposition, take the aluminium salt of decomposed as Al2O 3Then presoma mixes with the fused-salt medium (and crystal seed) of appropriate amount. After drying, at high temperature calcining. Fused-salt medium is removed in washing, can obtain tabular Al2O 3Particle. Main technologic parameters is as follows:
1. used aluminium salt is at high temperature can be decomposed into Al2O 3Sulfate or the nitrate of aluminium, as be Al2(SO 4) 3、 NH 4Al(SO 4) 2And Al (NO3) 3In a kind of, so-called part heat decomposition temperature refers to the temperature that aluminium salt begins to decompose in the crucible of heating
2. the inorganic salts that use as fused-salt medium are Na2SO 4、K 2SO 4, one or more the salt-mixture among NaCl and the KCl; Addition is that aluminium salt is decomposed into Al fully2O 3After, Al in the reaction system2O 3And the volume ratio of fused-salt medium is 1: 5-1: between 10.
3. tabular Al2O 3The addition of crystal seed is that aluminium salt is decomposed into Al fully2O 3Al in the afterreaction system2O 3The 5-40 wt% of total amount.
4. the molten salt system calcining heat is 1100-1300 ℃, and the reaction time is 1-3 hour.
Outstanding advantages of the present invention is:
With the aluminium salt of decomposed as Al2O 3Prepared tabular Al originates2O 3Particle is tiny evenly, and almost without reuniting, particle size is between sub-micron is to several microns. Again by adding tabular Al2O 3Crystal seed can accurately be controlled tabular Al in the end product2O 3The size of particle. Material preparation process is simple, is suitable for industrialized mass production. (seeing embodiment 3 for details)
Description of drawings:
Fig. 1 and 2 is respectively prepared tabular Al in embodiment 1 and 22O 3The stereoscan photograph of particle.
Fig. 3 adds (A) 5wt%, (B) 20.7wt% and (C) the tabular Al of 37wt% among the embodiment 32O 3Gained Al during crystal seed2O 3The stereoscan photograph of particle.
Fig. 4 is tabular Al among the embodiment 32O 3Granular size and tabular Al2O 3The relation curve of seed load, wherein solid line is the theoretical curve that calculates according to the Oswald growth mechanism, and loose point is concrete experimental result.
The specific embodiment
Limit by no means this explanation below in conjunction with the further specifying innovative point of the present invention of embodiment description.
Embodiment 1
At first, with Al2(SO 4) 3Place Al2O 3In the crucible, cover crucible cover, then making it decomposed in 3 hours in 900 ℃ of calcinings is Al2O 3 Secondly, with the Al of decomposed2(SO 4) 3With an amount of Na2SO 4Mix by ball milling, the raw material proportioning of mixed powder is for making Al2(SO 4) 3The Al that generates after decomposing fully2O 3With Na2SO 4The volume ratio of fused-salt medium is 1: 6. Above-mentioned mixed powder is placed on uncovered Al through 80 ℃ of dryings2O 3Calcined 1 hour for 1100 ℃ in the crucible. Product is through repeatedly getting rid of Na after the washing2SO 4, Fig. 1 is the tabular Al of gained six sides2O 3The stereoscan photograph of particle. Al2O 3Particle is monodispersed six side's plate-like particles almost, and size uniform (1 ± 0.1 μ m).
Embodiment 2
At first, with Al2(SO 4) 3Place Al2O 3In the crucible, cover crucible cover, then making it decomposed in 3 hours in 900 ℃ of calcinings is Al2O 3 Secondly, with the Al of decomposed2(SO 4) 3With an amount of Na2SO 4Mix by ball milling, the raw material proportioning of mixed powder is for making Al2(SO 4) 3The Al that generates after decomposing fully2O 3With Na2SO 4The volume ratio of fused-salt medium is 1: 8. Above-mentioned mixed powder is placed on uncovered Al through 80 ℃ of dryings2O 3Calcined 2 hours for 1200 ℃ in the crucible. Product is through repeatedly getting rid of Na after the washing2SO 4, Fig. 2 is the tabular Al of gained six sides2O 3The stereoscan photograph of particle. Al2O 3Particle is similarly almost monodispersed six side's plate-like particles, and average grain diameter is 960 ± 120nm.
Embodiment 3
Embodiment 3 is almost completely identical with the technical process of embodiment 2, and difference is that adding 5-40wt% particle diameter is the tabular Al of six sides of 1 μ m in material powder ball milling mixed process2O 3Particle is as crystal seed. Fig. 3 (A), (B) and (C) to be respectively seed load be 5,20.7 and the tabular Al of gained during 37wt%2O 3The stereoscan photograph of particle. Al in each sample2O 3Particle is approximate six side's plate-like particles, and its average grain diameter changes with the content of crystal seed. Further research is found, is adding tabular Al2O 3In the situation of crystal seed, Al in the powder2O 3Particle is take tabular crystal seed as template, grows according to the Oswald growth mechanism; Cause thus tabular Al in the final powder2O 3The size of particle size and crystal seed and content should have following relation, that is: D f = D s W s 3 , D whereinfAnd DsBe respectively in the final powder and crystal seed in tabular Al2O 3Particle size, WsWeight percent content for crystal seed. Fig. 4 is Al among the embodiment 32O 3The relation curve of plate-like particles size and crystal seed content, wherein loose point is concrete experimental result, and curve is the notional result of calculating according to above-mentioned formula. Can find that the two has good anastomose property. Therefore, according to above-mentioned formula, can realize Al in the final powder by the content that changes crystal seed2O 3The accurate control of plate-like particles size.

Claims (9)

1. tabular Al2O 3The preparation method of particle is characterized in that at first the calcining of aluminium salt is made it the part thermal decomposition, take the aluminium salt of decomposed as Al2O 3Then presoma mixes with the fused-salt medium ball milling; After drying, at high temperature calcining, fused-salt medium is removed in washing, obtains tabular Al2O 3Particle;
1. described aluminium salt is at high temperature being decomposed into Al2O 3Sulfate or the nitrate of aluminium;
2. the inorganic salts that use as fused-salt medium are Na2SO 4、K 2SO 4, one or more the salt-mixture among NaCl and the KCl; Addition is that aluminium salt is decomposed into Al fully2O 3After, Al in the reaction system2O 3And the volume ratio of fused-salt medium is 1: 5-1: between 10;
3. last calcining heat is 1100~1300 ℃.
2. by tabular Al claimed in claim 12O 3The preparation method of particle is characterized in that described aluminium salt is Al2(SO 4) 3、NH 4Al(SO 4) 2And Al (NO3) 3In any one.
3. by tabular Al claimed in claim 12O 3The method of particle is characterized in that Al2O 3The mixed dry rear calcination reaction time of the aluminium salt of decomposed and fused-salt medium is 1-3 hour.
4. by tabular Al claimed in claim 12O 3The method of particle is characterized in that the tabular Al for preparing2O 3Size is between sub-micron and several micron.
5. tabular Al2O 3The method of particle is characterized in that at first the calcining of aluminium salt is made it the part thermal decomposition, take the aluminium salt of decomposed as Al2O 3Then presoma mixes with fused-salt medium and crystal seed ball milling; After drying, at high temperature calcining, fused-salt medium is removed in washing, can obtain tabular Al2O 3Particle; Main technologic parameters is as follows:
1. used aluminium salt is Al2(SO 4) 3、NH 4Al(SO 4) 2And Al (NO3) 3Deng at high temperature being decomposed into Al2O 3Salt;
2. the inorganic salts that use as fused-salt medium are Na2SO 4、K 2SO 4, one or more the salt-mixture among NaCl and the KCl; Addition is that aluminium salt is decomposed into Al fully2O 3After, Al in the reaction system2O 3And the volume ratio of fused-salt medium is 1: 5-1: between 10;
3. described crystal seed is tabular Al2O 3Crystal seed, addition are that aluminium salt is decomposed into Al fully2O 3Al in the afterreaction system2O 3The 5-40wt% of total amount;
4. last calcining heat is 1100-1300 ℃.
6. by tabular Al claimed in claim 52O 3The preparation method of particle is characterized in that described aluminium salt is Al2(SO 4) 3、NH 4Al(SO 4) 2And Al (NO3) 3In any one.
7. by tabular Al claimed in claim 52O 3The method of particle is characterized in that Al2O 3The mixed dry rear calcination reaction time of the aluminium salt of decomposed and fused-salt medium is 1-3 hour.
8. by the preparation method of the described plate-like aluminum oxide of any one claim in the claim 5 to 7, it is characterized in that the plate-like aluminum oxide granule of final preparation is take tabular crystal seed as template, tabular Al in the final powder2O 3The size of particle size and crystal seed and the relational expression of content are D f = D s W s 3 , D in the formulafAnd DsBe respectively in the final powder and crystal seed in tabular Al2O 3Particle size, WsWeight percentage for crystal seed.
9. by tabular Al claimed in claim 52O 3The method of particle is characterized in that the tabular Al for preparing2O 3Size is between sub-micron and several micron.
CNB2006100233238A 2006-01-13 2006-01-13 Plate-like aluminum oxide granule preparation method Expired - Fee Related CN100378002C (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101182024B (en) * 2007-11-23 2010-04-14 清华大学 Method for preparing one-dimensional aluminum oxide fibre by hydrothermal-flux technique
CN101844784A (en) * 2010-05-21 2010-09-29 山东大学 Alpha-Al2O3 nanostructure aggregate material and preparation method thereof
CN101891226A (en) * 2010-07-27 2010-11-24 林仕冯 Flaky alumina and preparation method thereof
CN102849768A (en) * 2012-09-19 2013-01-02 蚌埠鑫源石英材料有限公司 Preparation method of tabular alpha-aluminum oxide
CN104986786A (en) * 2015-07-31 2015-10-21 华南理工大学 Sheet alpha-Al2O3 powder body with controllable particle diameter size and preparation method of sheet alpha-Al2O3 powder body
CN107326432A (en) * 2017-06-30 2017-11-07 哈尔滨工业大学 A kind of preparation method and application of the template seed crystal of texture aluminium oxide ceramics

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5277702A (en) * 1993-03-08 1994-01-11 St. Gobain/Norton Industrial Ceramics Corp. Plately alumina
CN1076716C (en) * 1997-12-16 2001-12-26 武汉工业大学 Process for mfg. non-lumps submicron alpha-Al2O3 powder and microlitic corundum ball
JP2000247634A (en) * 1999-02-25 2000-09-12 Ykk Corp Production of alumina tabular grain
CN1131185C (en) * 2000-12-29 2003-12-17 清华大学 Process for preparing high-toughness alumina ceramics
TW200422258A (en) * 2003-02-26 2004-11-01 Sumitomo Chemical Co Method for producing α-alumina powder
JP4572576B2 (en) * 2003-05-19 2010-11-04 住友化学株式会社 Method for producing fine α-alumina

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101182024B (en) * 2007-11-23 2010-04-14 清华大学 Method for preparing one-dimensional aluminum oxide fibre by hydrothermal-flux technique
CN101844784A (en) * 2010-05-21 2010-09-29 山东大学 Alpha-Al2O3 nanostructure aggregate material and preparation method thereof
CN101891226A (en) * 2010-07-27 2010-11-24 林仕冯 Flaky alumina and preparation method thereof
CN101891226B (en) * 2010-07-27 2012-07-04 林仕冯 Flaky alumina and preparation method thereof
CN102849768A (en) * 2012-09-19 2013-01-02 蚌埠鑫源石英材料有限公司 Preparation method of tabular alpha-aluminum oxide
CN104986786A (en) * 2015-07-31 2015-10-21 华南理工大学 Sheet alpha-Al2O3 powder body with controllable particle diameter size and preparation method of sheet alpha-Al2O3 powder body
CN107326432A (en) * 2017-06-30 2017-11-07 哈尔滨工业大学 A kind of preparation method and application of the template seed crystal of texture aluminium oxide ceramics
CN107326432B (en) * 2017-06-30 2019-07-02 哈尔滨工业大学 A kind of preparation method and application of the template seed crystal of texture aluminium oxide ceramics

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