CN102992626A - Preparation method of Li, Mg, Al and Si glass ceramic foundation powder - Google Patents

Preparation method of Li, Mg, Al and Si glass ceramic foundation powder Download PDF

Info

Publication number
CN102992626A
CN102992626A CN2012104910986A CN201210491098A CN102992626A CN 102992626 A CN102992626 A CN 102992626A CN 2012104910986 A CN2012104910986 A CN 2012104910986A CN 201210491098 A CN201210491098 A CN 201210491098A CN 102992626 A CN102992626 A CN 102992626A
Authority
CN
China
Prior art keywords
lithium
silicon
preparation
glass ceramic
oxide
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.)
Pending
Application number
CN2012104910986A
Other languages
Chinese (zh)
Inventor
岳丹
蒋达光
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.)
Jiangsu Yida Photoelectric Science & Technology Co Ltd
Original Assignee
Jiangsu Yida Photoelectric Science & Technology Co Ltd
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 Jiangsu Yida Photoelectric Science & Technology Co Ltd filed Critical Jiangsu Yida Photoelectric Science & Technology Co Ltd
Priority to CN2012104910986A priority Critical patent/CN102992626A/en
Publication of CN102992626A publication Critical patent/CN102992626A/en
Pending legal-status Critical Current

Links

Landscapes

  • Glass Compositions (AREA)

Abstract

The invention relates to a preparation method of glass ceramic foundation powder, and in particular relates to a preparation method of Li, Mg, Al and Si glass ceramic foundation powder. Main raw materials comprise 55-65% of silicon dioxide, 12-18% of aluminium sesquioxide, 5-6% of lithium oxide, 1-3% of chromic oxide, 5-7% of magnesium fluoride, 3-4% of zirconium oxide and 0.3-0.6% of antimony oxide; and the preparation method comprises that the raw materials are mixed and then heated, and then water quenching and smashing are carried out, so that the glass ceramic foundation powder is obtained. The Li, Mg, Al and Si glass ceramic foundation powder provided by the invention has the advantages that glass liquid after melting is clear, viscosity is low and crystal growth rate is increased.

Description

Lithium magnalium silicon devitrified glass basic powder preparation method
Technical field
The present invention relates to a kind of preparation method of devitrified glass basic powder, be specially lithium magnalium silicon devitrified glass basic powder preparation method.
Background technology
The characteristics such as lithium magnalium silicon devitrified glass has that thermal expansivity is low, dimensional stability is high, heat shock resistance and chemical stability are good, but in the heat treatment process of lithium magnalium silicon crystallite parent glass powder, glass precursor solution viscosity is large, crystalline growth velocity is slower.
Summary of the invention
In order to solve the problems of the technologies described above, the invention provides a kind of lithium magnalium silicon devitrified glass basic powder preparation method that can reduce glass viscosity, improve crystalline growth velocity, concrete technical scheme is:
(1) takes by weighing raw material according to following weight percent prescription and mix, silicon-dioxide 55-65%, aluminium sesquioxide 12-18%, Lithium Oxide 98min 5-6%, chromic oxide 1-3%, magnesium fluoride 5-7%, zirconium white 3-4%, weisspiessglanz 0.3-0.6%;
(2) above-mentioned raw materials is heated to 1450 ℃ after mixing in crucible, and is incubated 2 hours;
(3) glass precursor solution is poured into carried out shrend in the water quenching pool and become glass particle;
(4) ball milling is 1 hour, and dry rear 200 mesh sieves of crossing namely get lithium magnalium silicon devitrified glass basic powder.
The optimization formula ratio is: silicon-dioxide 61%, aluminium sesquioxide 16.3%, Lithium Oxide 98min 5.5%, chromic oxide 2.0%, magnesium fluoride 6.5%, zirconium white 3.2%, weisspiessglanz 0.5%.
 
Lithium magnalium silicon devitrified glass basic powder provided by the invention, glass precursor solution clarification and viscosity are little after the fusing, and optimum treatment condition is: 786 degrees centigrade of crystallization temperatures, and reduced temperature of fusion, improved crystalline growth velocity.
Embodiment
Lithium magnalium silicon devitrified glass basic powder preparation method, concrete technical scheme is:
(1) taking by weighing raw material according to following weight percent prescription mixes:
Silicon-dioxide 61%, aluminium sesquioxide 16.3%, Lithium Oxide 98min 5.5%, chromic oxide 2.0%, magnesium fluoride 6.5%, zirconium white 3.2%, weisspiessglanz 0.5%;
(2) in crucible, be heated to 1450 ℃ take heat-up rate as 10 ℃/minute after above-mentioned raw materials mixes, and be incubated 2 hours;
(3) glass precursor solution is poured into carried out shrend in the water quenching pool and become glass particle;
(4) ball milling is 1 hour, and dry rear 200 mesh sieves of crossing namely get lithium magnalium silicon devitrified glass basic powder.
This parent glass powder is warming up to rapidly 786 degrees centigrade of crystallization temperatures take heat-up rate as 10 ℃/minute speed, and is incubated 2 hours, separate out bar-shaped β-triphane sosoloid crystalline phase under this condition, crystal length is 2-5 μ m, and length-to-diameter ratio is larger.

Claims (2)

1. lithium magnalium silicon devitrified glass basic powder preparation method is characterized in that: may further comprise the steps,
(1) takes by weighing raw material according to following weight percent prescription and mix, silicon-dioxide 55-65%, aluminium sesquioxide 12-18%, Lithium Oxide 98min 5-6%, chromic oxide 1-3%, magnesium fluoride 5-7%, zirconium white 3-4%, weisspiessglanz 0.3-0.6%;
(2) above-mentioned raw materials is heated to 1450 ℃ after mixing in crucible, and is incubated 2 hours;
(3) glass precursor solution is poured into carried out shrend in the water quenching pool and become glass particle;
(4) ball milling is 1 hour, and dry rear 200 mesh sieves of crossing namely get lithium magnalium silicon devitrified glass basic powder.
2. lithium magnalium silicon devitrified glass basic powder preparation method according to claim 1, it is characterized in that: described prescription is silicon-dioxide 61%, aluminium sesquioxide 16.3%, Lithium Oxide 98min 5.5%, chromic oxide 2.0%, magnesium fluoride 6.5%, zirconium white 3.2%, weisspiessglanz 0.5%.
CN2012104910986A 2012-11-28 2012-11-28 Preparation method of Li, Mg, Al and Si glass ceramic foundation powder Pending CN102992626A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2012104910986A CN102992626A (en) 2012-11-28 2012-11-28 Preparation method of Li, Mg, Al and Si glass ceramic foundation powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2012104910986A CN102992626A (en) 2012-11-28 2012-11-28 Preparation method of Li, Mg, Al and Si glass ceramic foundation powder

Publications (1)

Publication Number Publication Date
CN102992626A true CN102992626A (en) 2013-03-27

Family

ID=47921816

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2012104910986A Pending CN102992626A (en) 2012-11-28 2012-11-28 Preparation method of Li, Mg, Al and Si glass ceramic foundation powder

Country Status (1)

Country Link
CN (1) CN102992626A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9850172B2 (en) 2014-10-23 2017-12-26 Industrial Technology Research Institute Ceramic powder, method of manufacturing the same, and method for laser sinter molding

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3715196A (en) * 1970-09-02 1973-02-06 Corning Glass Works Low-expansion glass-ceramic cementing method
CN1087067A (en) * 1992-11-18 1994-05-25 大连理工大学 Utilize flyash to make building nucleated glass
WO2005009916A1 (en) * 2003-07-28 2005-02-03 Kabushiki Kaisha Ohara Negative thermal expansion glass ceramic

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3715196A (en) * 1970-09-02 1973-02-06 Corning Glass Works Low-expansion glass-ceramic cementing method
CN1087067A (en) * 1992-11-18 1994-05-25 大连理工大学 Utilize flyash to make building nucleated glass
WO2005009916A1 (en) * 2003-07-28 2005-02-03 Kabushiki Kaisha Ohara Negative thermal expansion glass ceramic

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
周曦亚等: "含F-锂镁铝硅微晶玻璃的制备及晶化行为的研究", 《材料导报》, no. 1, 25 November 2009 (2009-11-25) *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9850172B2 (en) 2014-10-23 2017-12-26 Industrial Technology Research Institute Ceramic powder, method of manufacturing the same, and method for laser sinter molding

Similar Documents

Publication Publication Date Title
JP6546276B2 (en) High hardness transparent crystalline glass and method for preparing the same
CN101580343B (en) Rare earth-mixing high strength lithium bisilicate sitall material and preparation method thereof
CN101381240B (en) Method for preparing dichroite heat proof/refractory materials
US20120094822A1 (en) Lithium silicate glass ceramic for fabrication of dental appliances
CN109265011A (en) A kind of preparation method of magnesium al-si system glass and high-crystallinity transparent glass-ceramics
JP5770050B2 (en) Crystallized glass having negative coefficient of thermal expansion and method for producing the same
CN101215091A (en) Preparation method of leadless glass powder for electronic slurry
CN105347685A (en) Glass ceramic and preparation method thereof
CN104445952B (en) A kind of high-hard, transparent devitrified glass and preparation method thereof
CN102543237B (en) Glass solidified body and preparation method thereof
CN105314852A (en) Rare earth doped CaO-Al2O3-SiO2 transparent glass ceramic and preparation method thereof
CN100352782C (en) Glass ceramic containing phosphorus lithium aluminium silicon and its preparation method
CN102992626A (en) Preparation method of Li, Mg, Al and Si glass ceramic foundation powder
CN1315747C (en) Glass ceramic containing fluorine phosphorus lithium aluminium silican and its preparation method
CN111170642A (en) High-strength high-toughness low-expansion lithium-aluminum-silicon transparent glass ceramic and preparation method thereof
CN104478219A (en) Nano-scale spinel glass ceramic and preparation method thereof
CN102557444A (en) Method for preparing glass ceramic from serpentine tailings
Bao et al. Effect of B2O3 and P2O5 Addition on the Phase Separation and Crystallization of Li2O-MgO-Al2O3-SiO2 Glass-Ceramics
CN102689928A (en) Preparation method of near-stoichiometric lithium tantalate crystals
WO2012065300A1 (en) Method for preparing microcrystalline glass-ceramics faceplate
CN102689927A (en) Preparation method of near-stoichiometric lithium niobate crystals
CN101844868B (en) Purplish-red glass-ceramic containing neodymium and preparation method thereof
CN110104948A (en) It is the heat-resistant opal glass and preparation method thereof of raw material preparation using recessed soil
CN110577359B (en) Fluorapatite and zinc spinel phase bioglass and biological glass ceramics and preparation method thereof
CN101774765A (en) Frit of fuse substrate in monolithic structure and manufacture 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
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20130327