[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

CN103395984B - Method for reducing microbubbles of alumina silicate glass - Google Patents

Method for reducing microbubbles of alumina silicate glass Download PDF

Info

Publication number
CN103395984B
CN103395984B CN201310355029.7A CN201310355029A CN103395984B CN 103395984 B CN103395984 B CN 103395984B CN 201310355029 A CN201310355029 A CN 201310355029A CN 103395984 B CN103395984 B CN 103395984B
Authority
CN
China
Prior art keywords
amount
particle diameter
accounts
total
particles
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.)
Active
Application number
CN201310355029.7A
Other languages
Chinese (zh)
Other versions
CN103395984A (en
Inventor
彭寿
王芸
马立云
崔介东
曹欣
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.)
China Triumph International Engineering Co Ltd
Bengbu Glass Industry Design and Research Institute
Original Assignee
China Triumph International Engineering Co Ltd
Bengbu Glass Industry Design and Research Institute
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 China Triumph International Engineering Co Ltd, Bengbu Glass Industry Design and Research Institute filed Critical China Triumph International Engineering Co Ltd
Priority to CN201310355029.7A priority Critical patent/CN103395984B/en
Publication of CN103395984A publication Critical patent/CN103395984A/en
Application granted granted Critical
Publication of CN103395984B publication Critical patent/CN103395984B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Glass Compositions (AREA)

Abstract

The invention relates to a method for reducing microbubbles of a piece of alumina silicate glass. The optimal founding and homogenization effects are realized by special grain size distribution of glass batch, the alumina silicate glass with fewer bubbles and small diameter bubbles is obtained, and the use requirement of the special glass for electronic information display is met. Specifically, the granular size of the glass batch such as feldspar, silica sand, dolomite, limestone, sodium carbonate and mirabilite is controlled to be in a specific range, due to the optimization and matching of larger granular raw materials and smaller granular raw materials, the reaction homogeneity and completeness of the batch are realized, the optimal founding effect is realized, and the excellent alumina silicate glass with fewer bubbles and small diameter bubbles is obtained.

Description

A kind of method reducing alumina silicate glass microbubble
Technical field
The present invention relates to the preparation method of alumina silicate glass, the particular level of granularity formula formula particularly by controlling admixtion realizes the method that alumina silicate glass microbubble reduces.
Background technology
In glass melting process, bubble is a kind of defect the most common, and it can affect the outward appearance of glasswork, transparency, physical strength and hardness etc., when remaining have the glass of some amount microbubble to show for electronic information time, will be fatal.
Summary of the invention
Object of the present invention is in order to solve the defect of the some amount microbubble of existing alumina silicate glass existence, the a kind of of proposition realizes the better technical scheme with homo-effect of founding with the specific grain size distribution of admixtion, obtains the alumina silicate glass that number of bubbles is few, bubble diameter is little.
The technical solution used in the present invention is as follows:
A kind of method reducing alumina silicate glass microbubble, comprise the alumina silicate glass admixtion be made up of following raw material: feldspar, silica sand, rhombspar, Wingdale, soda ash, saltcake, the component of the alumina silicate glass made is counted by the mass percent of oxide compound: SiO2 62 ~ 65wt.%; Al2O3 12 ~ 15wt.%; MgO 1 ~ 4wt.%; CaO 1 ~ 3wt.%; Na2O 11 ~ 15wt.%; K2O 1 ~ 3wt.%, is characterized in that: the raw material granularity grating mode prepared in the admixtion of alumina silicate glass is carried out according to following proportioning:
(1) feldspar: particle diameter is the 75wt.% that the feldspar amount of particles of 0.1 ~ 0.25mm accounts for total feldspar amount, particle diameter is the 25wt.% that the feldspar amount of particles of 0.4 ~ 0.55mm accounts for total feldspar amount;
(2) rhombspar: particle diameter is the 15wt.% that the dolomite particles consumption of 0.075 ~ 0.125mm accounts for total rhombspar amount, particle diameter is the 85wt.% that the dolomite particles consumption of 2.0 ~ 2.5mm accounts for total rhombspar amount;
(3) Wingdale: particle diameter is the 15wt.% that the limestone particle consumption of 0.08 ~ 0.15mm accounts for total Wingdale amount, particle diameter is the 85wt.% that the limestone particle consumption of 2.5 ~ 3.0mm accounts for total Wingdale amount;
(4) silica sand: particle diameter is the 90wt.% that the silica sand particles consumption of 0.1 ~ 1mm accounts for total silica sand amount, particle diameter is the 10wt.% that the silica sand particles consumption of 0.085 ~ 0.1mm accounts for total silica sand amount;
(5) soda ash: particle diameter is the 75wt.% that the soda ash amount of particles of 0.1 ~ 1mm accounts for total soda ash amount, particle diameter is the 25wt.% that the soda ash amount of particles of 0.055 ~ 0.1mm accounts for total soda ash amount;
(6) saltcake: particle diameter is the 90wt.% that the saltcake amount of particles of 0.1 ~ 1mm accounts for total saltcake amount, particle diameter is the 10wt.% that the saltcake amount of particles of 0.08 ~ 0.1mm accounts for total saltcake amount.
On the basis of technique scheme, following further technical scheme can be had:
The admixtion of described grain size distribution is fired according to the following steps:
(1) rise to 1630 DEG C with the temperature rise rate of 3 ~ 5 DEG C/min by room temperature, and be incubated 2 ~ 3 hours;
(2) be down to 1610 DEG C with the rate of temperature fall of 1 ~ 3 DEG C/min by 1630 DEG C, and be incubated 1.5 ~ 2 hours;
(3) at 1610 DEG C of temperature, the shaping of glass metal is carried out;
(4) in the temperature range of 600 ~ 750 DEG C, shaping glasswork is carried out anneal.
The existence of microbubble in glass, is mainly reacted by the fusing of admixtion in melting process that incomplete sum glass metal homogenizing is insufficient to be caused, and the granularity of frit then has influence on fusing and the homogenizing of glass.The granularity of frit is less, and the contact area between raw material is larger, and reaction surface is also larger, thus speed of response between raw material is also larger, and on the contrary, when raw material granularity is bigger than normal, the speed reacted between raw material is comparatively slow, makes burn-off rate slack-off.If but raw material granularity is too small, then easily produce and fly upward and lump, the raw material that granularity is less simultaneously can participate in reaction prematurely, causes admixtion to found layering, also can affect founding of glass, be unfavorable for the homogenizing of glass.Therefore, the size classification how controlling glass batch is the key obtaining the high quality glass that entrapped air pockets quantity is few and bubble diameter is little.
A kind of method reducing alumina silicate glass microbubble provided by the invention, by the specified particle size grating of glass batch, namely in same admixtion, the intergranular optimization of different-grain diameter, what realize the best founds effect, obtains the fine aluminum silicate glass that bubbles number is few, bubble diameter is little.
Accompanying drawing explanation
Fig. 1, Fig. 2 and Fig. 3 bubble picture for utilizing the inside of the alumina silicate glass captured by super depth-of-field microscope remaining, for amplifying the effect after 100 times;
Fig. 1 and Fig. 2 is the bubble picture of the alumina silicate glass sample not adopting the admixtion of grain size distribution to fire;
Fig. 3 is the bubble picture of the alumina silicate glass sample that the grain size distribution mode adopting the present invention to propose is fired.
Embodiment
Below in conjunction with specific embodiment, the present invention is set forth in detail.
Embodiment:
1, using feldspar, silica sand, rhombspar, Wingdale, soda ash, saltcake as the raw material of burning glass, the chemical constitution of various raw material is as shown in table 1.
The chemical constitution (wt.%) of table 1 raw material
2, consisting of of the glass oxide will fired: SiO 265wt.%; Al 2o 314wt.%; MgO 2wt.%; CaO 3wt.%; Na 2o 13wt.%; K 2o 2wt.%.
3, according to the content of oxide compound in the above-mentioned glass composition that will fire, calculate the consumption of each admixtion respectively, in admixtion, add a certain amount of carbon dust, their consumption is as shown in table 2 simultaneously.
Table 2 admixtion scale
Material name Feldspar Silica sand Rhombspar Wingdale Soda ash Saltcake Carbon dust
Quality (g) 312 52 36.8 1.9 90.8 8 0.24
4, then by admixtion, choose raw material by following grain size distribution mode and sieve out the particle of corresponding particle size range, mixing fully.
(1) feldspar: sieve and take the feldspar particle 234 grams that particle diameter is 0.1 ~ 0.25mm, sieves and takes the feldspar particle 78 grams that particle diameter is 0.4 ~ 0.55mm;
(2) rhombspar: sieve and take the dolomite particles 5.52 grams that particle diameter is 0.075 ~ 0.125mm, sieves and takes the dolomite particles 31.3 grams that particle diameter is 2.0 ~ 2.5mm;
(3) Wingdale: sieve and take the limestone particle 0.29 gram that particle diameter is 0.08 ~ 0.15mm, sieves and takes the limestone particle 1.62 grams that particle diameter is 2.5 ~ 3.0mm;
(4) silica sand: sieve and take the silica sand particles 46.8 grams that particle diameter is 0.1 ~ 1mm, sieves and takes the silica sand particles 5.2 grams that particle diameter is 0.085 ~ 0.1mm;
(5) soda ash: sieve and take the soda ash particle 68.1 grams that particle diameter is 0.1 ~ 1mm; Sieve and take the soda ash particle 22.7 grams that particle diameter is 0.055 ~ 0.1mm;
(6) saltcake: sieve and take the saltcake particle 7.2 grams that particle diameter is 0.1 ~ 1mm, sieves and takes the saltcake particle 0.8 gram that particle diameter is 0.08 ~ 0.1mm.
After above-mentioned admixtion Homogeneous phase mixing, carry out founding of glass by following melting system:
(1) rise to 1630 DEG C by room temperature with the temperature rise rate of 2.5 DEG C/min, and be incubated 2.5 hours;
(2) be down to 1610 DEG C with the rate of temperature fall of 2 DEG C/min by 1630 DEG C, and be incubated 2 hours;
(3) at 1610 DEG C of temperature, the shaping of glass metal is carried out;
(4) at the temperature of 720 DEG C, shaping glasswork is carried out anneal.
Obtain the alumina silicate glass that remaining microbubble quantity is few, bubble diameter is little thus, as shown in Figure 3, the microbubble picture of the inside glass of the amplification of taking for utilizing super depth-of-field microscope 100 times.And Fig. 1 is melting system same as the previously described embodiments and the bubble picture of the aluminosilicate glass article of identical oxide compound proportioning, difference is, it is not according to grain size distribution mode of the present invention, but identical granularity all selected by all admixtiones, for the particle size that relative the present invention is larger, be 0.2 ~ 0.5mm; And Fig. 2 is all raw material particle sizes is the less particle size of relative the present invention, be 0.05 ~ 0.1mm.From Fig. 1, Fig. 2 and Fig. 3 relatively, the grain size distribution mode that the present invention proposes effectively can reduce the remaining number of bubbles of alumina silicate glass and bubble diameter, meets the requirement of electronic information display special glass.
The above, be only preferred embodiment of the present invention, not does any pro forma restriction to the present invention; Any those of ordinary skill in the art, do not departing under technical solution of the present invention ambit, the Method and Technology content of above-mentioned announcement can be utilized to make many possible variations and modification to technical solution of the present invention, or be revised as the Equivalent embodiments of equivalent variations.Therefore, every content not departing from technical solution of the present invention, any simple modification done above-described embodiment according to technical spirit of the present invention, equivalent replacement, equivalence change and modification, all still belong in the scope of technical solution of the present invention protection.

Claims (1)

1. one kind is reduced the method for alumina silicate glass microbubble, comprise the alumina silicate glass admixtion be made up of following raw material: feldspar, silica sand, rhombspar, Wingdale, soda ash, saltcake, the component of the alumina silicate glass made is counted by the mass percent of oxide compound: Si0 262 65wt.%; A1 20 312 15wt.%; MgO 1 4wt.%; CaO 1 3wt.%; Na 20 11 15wt.%; K 201 3wt.%, is characterized in that:
A, the raw material granularity grating mode prepared in the admixtion of alumina silicate glass are carried out according to following proportioning:
(1) feldspar: particle diameter is the 75wt.% that the feldspar amount of particles of 0.1 0.25mm accounts for total feldspar amount, particle diameter is the 25wt.% that the feldspar amount of particles of 0.4 0.55mm accounts for total feldspar amount;
(2) rhombspar: particle diameter is the 15wt.% that the dolomite particles consumption of 0.075 0.125mm accounts for total rhombspar amount, particle diameter is the 85wt.% that the dolomite particles consumption of 2.0 2.5mm accounts for total rhombspar amount;
(3) Wingdale: particle diameter is the 15wt.% that the limestone particle consumption of 0.08 0.15mm accounts for total Wingdale amount, particle diameter is the 85wt.% that the limestone particle consumption of 2.5 3.0mm accounts for total Wingdale amount;
(4) silica sand: particle diameter is the 90wt.% that the silica sand particles consumption of 0.1 1mm accounts for total silica sand amount, particle diameter is the 10wt.% that the silica sand particles consumption of 0.085 0.1mm accounts for total silica sand amount;
(5) soda ash: particle diameter is the 75wt.% that the soda ash amount of particles of 0.1 1mm accounts for total soda ash amount, particle diameter is the 25wt.% that the soda ash amount of particles of 0.055 0.1mm accounts for total soda ash amount;
(6) saltcake: particle diameter is the 90wt.% that the saltcake amount of particles of 0.1 1 mm accounts for total saltcake amount, particle diameter is the 10wt.% that the saltcake amount of particles of 0.08 0.1mm accounts for total saltcake amount;
The admixtion of B, described grain size distribution is fired according to the following steps:
(1) with 35 ° of C/minute temperature rise rate rise to 1630 ° of C by room temperature, and be incubated 23 hours;
(2) with 13 ° of C/minute rate of temperature fall be down to 1610 ° of C by 1630 ° of C, and be incubated 1. 52 hours;
(3) at 1610 ° of C temperature, the shaping of glass metal is carried out;
(4) in the temperature range of 600 750 ° of C, shaping glasswork is carried out anneal.
CN201310355029.7A 2013-08-15 2013-08-15 Method for reducing microbubbles of alumina silicate glass Active CN103395984B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310355029.7A CN103395984B (en) 2013-08-15 2013-08-15 Method for reducing microbubbles of alumina silicate glass

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310355029.7A CN103395984B (en) 2013-08-15 2013-08-15 Method for reducing microbubbles of alumina silicate glass

Publications (2)

Publication Number Publication Date
CN103395984A CN103395984A (en) 2013-11-20
CN103395984B true CN103395984B (en) 2015-07-08

Family

ID=49559778

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310355029.7A Active CN103395984B (en) 2013-08-15 2013-08-15 Method for reducing microbubbles of alumina silicate glass

Country Status (1)

Country Link
CN (1) CN103395984B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3395772A4 (en) * 2015-12-25 2019-08-07 Nippon Electric Glass Co., Ltd. Mixed material for silicate glass and method for manufacturing tube glass using same
WO2018088503A1 (en) * 2016-11-14 2018-05-17 旭硝子株式会社 Production method for molten glass and production method for glass article
CN107010833A (en) * 2017-04-06 2017-08-04 蚌埠玻璃工业设计研究院 A kind of preparation method of thin-film solar cells glass substrate
CN109279775A (en) * 2017-07-19 2019-01-29 王奔强 A kind of glass processing method
CN108483901A (en) * 2018-06-05 2018-09-04 中建材蚌埠玻璃工业设计研究院有限公司 A kind of alkali-free glass batch of silicon sand size grading
CN109626831A (en) * 2019-01-16 2019-04-16 河南光远新材料股份有限公司 A method of reducing residual microbubbles in electronic glass fibers

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102976587A (en) * 2012-12-22 2013-03-20 蚌埠玻璃工业设计研究院 Clarification method of alumina silicate glass melts

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102009011850B3 (en) * 2009-03-05 2010-11-25 Schott Ag Process for the environmentally friendly melting and refining of a glass melt for a starting glass of a lithium-aluminum-silicate (LAS) glass ceramic and their use

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102976587A (en) * 2012-12-22 2013-03-20 蚌埠玻璃工业设计研究院 Clarification method of alumina silicate glass melts

Also Published As

Publication number Publication date
CN103395984A (en) 2013-11-20

Similar Documents

Publication Publication Date Title
CN103395984B (en) Method for reducing microbubbles of alumina silicate glass
JP5719806B2 (en) Manufacturing method of glass substrate for information display device, and glass substrate for information display device obtained by this manufacturing method
CN100404472C (en) Leadless molten block enamel for bone porcelain
JP2022550970A (en) Lithium zirconium aluminosilicate glass, tempered glass, manufacturing method thereof and display parts
CN107162410B (en) Glass and preparation method thereof
KR20160006715A (en) Alkali-free phosphoborosilicate glass
CN101638293B (en) High-performance glass frit block for producing glass microfiber and preparation method thereof
ATE479635T1 (en) GLASS COMPOSITIONS
CN101891501A (en) Lead-free and cadmium-free bone china glaze and preparation process thereof
CN102992812A (en) Microcrystal-reinforced transparent leadless fritted glaze and preparation method thereof
CN101585717A (en) Lead and cadmium free fritted glaze for bone China with high acid resistance and alkali resistance
WO2019080190A1 (en) Aluminosilicate glass and preparation method therefor, and electronic device
CN102249540A (en) Na2O-CaO-SiO2 opaque glass and preparation method thereof
JP2016113363A (en) Production method of silicate glass, silicate glass, and silica raw material for silicate glass
CN109320072B (en) High-aluminum low-calcium glass capable of being chemically strengthened
JP2010132541A (en) Method for producing alkali-free glass
CN102690057A (en) Glass formula used for new touch screen cover plate glass
CN105439532A (en) High-performance pottery and preparation method thereof
CN113735450A (en) Transparent high-hardness magnesium-aluminum-silicon microcrystalline glass and preparation method thereof
CN101186129B (en) Micro-crystallizing glass-ceramic composite board and producing method thereof
US20180354842A1 (en) Mixed raw material for silicate glass and method for manufacturing tube glass using same
JP3269416B2 (en) Crystallized glass and method for producing the same
CN102557433A (en) Solar glass for full-oxygen combustion tank furnace
JP2013107801A (en) Method for producing glass substrate
CN102515856A (en) Bone china lead-free glaze 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
EE01 Entry into force of recordation of patent licensing contract

Application publication date: 20131120

Assignee: In building materials (Bengbu) photoelectric material Co Ltd

Assignor: Bengbu design Institute of Glass Industry

Contract record no.: 2016340000005

Denomination of invention: Method for reducing microbubbles of alumina silicate glass

Granted publication date: 20150708

License type: Common License

Record date: 20160418

LICC Enforcement, change and cancellation of record of contracts on the licence for exploitation of a patent or utility model