JPH03223129A - Method for tempering sheet glass - Google Patents
Method for tempering sheet glassInfo
- Publication number
- JPH03223129A JPH03223129A JP1962690A JP1962690A JPH03223129A JP H03223129 A JPH03223129 A JP H03223129A JP 1962690 A JP1962690 A JP 1962690A JP 1962690 A JP1962690 A JP 1962690A JP H03223129 A JPH03223129 A JP H03223129A
- Authority
- JP
- Japan
- Prior art keywords
- gel
- metal alkoxide
- sintered
- sheet glass
- glass
- 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
Links
- 238000000034 method Methods 0.000 title claims description 9
- 239000005357 flat glass Substances 0.000 title description 5
- 238000005496 tempering Methods 0.000 title 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000004703 alkoxides Chemical class 0.000 claims abstract description 8
- 239000002184 metal Substances 0.000 claims abstract description 8
- 229910052751 metal Inorganic materials 0.000 claims abstract description 8
- 239000002994 raw material Substances 0.000 claims abstract description 3
- 238000003980 solgel method Methods 0.000 claims abstract description 3
- 238000005728 strengthening Methods 0.000 claims description 4
- 230000007062 hydrolysis Effects 0.000 claims description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 239000000499 gel Substances 0.000 abstract description 15
- 239000011240 wet gel Substances 0.000 abstract description 4
- 230000001413 cellular effect Effects 0.000 abstract 2
- 230000003301 hydrolyzing effect Effects 0.000 abstract 2
- 238000007598 dipping method Methods 0.000 abstract 1
- 239000011521 glass Substances 0.000 description 9
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000006059 cover glass Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 229910052789 astatine Inorganic materials 0.000 description 1
- 239000006121 base glass Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000013081 microcrystal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B19/00—Other methods of shaping glass
- C03B19/12—Other methods of shaping glass by liquid-phase reaction processes
Abstract
Description
【発明の詳細な説明】
「産業上の利用分野」
本発明は、腕時計のカバーガラスや各種基板などへの応
用を可能にする板状ガラスの強化方法に関する。DETAILED DESCRIPTION OF THE INVENTION "Field of Industrial Application" The present invention relates to a method for strengthening sheet glass, which enables application to cover glasses of wristwatches, various substrates, and the like.
[従来の技術]
従来のガラスの強化方法としては、イオン交換などによ
る表面処理、ガラス内部への微結晶析出、表面修飾など
が行なわれていた。[Prior Art] Conventional glass strengthening methods include surface treatment by ion exchange, precipitation of microcrystals inside the glass, and surface modification.
[発明が解決しようとする課題]
しかし、前述の従来技術においては、プロセスが複雑に
なるため、製造コストが高くなる。あるいは、他の成分
を導入することにより、本来の光学的特性が失なわれる
などの問題点を有する。[Problems to be Solved by the Invention] However, in the above-mentioned conventional technology, the process becomes complicated and the manufacturing cost increases. Alternatively, introducing other components may cause problems such as loss of original optical properties.
そこで、本発明の目的とするところは、基のガラスのも
つ強度以外の特性を維持した上で、容易に板状ガラスの
強度を向上させる方法を提供するところにある。Therefore, an object of the present invention is to provide a method for easily improving the strength of sheet glass while maintaining the properties other than the strength of the base glass.
口課題を解決するための手段]
本発明の板状ガラスの強化方法は、少なくとも金属アル
コキシドやシリカ粒子を原料とするゾル−ゲル法により
得られる多孔性の焼結ゲルを、金属アルコキシドの加水
分解溶液に浸漬し、表面付近に拡散させることを特徴と
する特
[作用]
本発明は、多孔性の焼結ゲル表面付近に、金属アルコキ
シドの加水分解溶液を拡散させた後、乾燥、焼結するた
め、焼結後のガラスには、表面付近に圧縮応力が生ずる
。これが、表裏2面に生じるため、内部に引っ張り応力
が生じ、全体としてガラス板の強度が向上するものであ
る。[Means for Solving the Problems] The method for strengthening sheet glass of the present invention is characterized in that a porous sintered gel obtained by a sol-gel method using at least metal alkoxide or silica particles as a raw material is prepared by hydrolysis of metal alkoxide. A special feature of the present invention is to diffuse a hydrolyzed solution of a metal alkoxide near the surface of a porous sintered gel, and then dry and sinter it. Therefore, compressive stress is generated near the surface of the glass after sintering. Since this occurs on both the front and back surfaces, tensile stress is generated inside, and the strength of the glass plate as a whole is improved.
[実施例]
エチルシリケート、エタノール、水、アンモニア水(2
9%)をモル比で1ニア、6:4:0.0Bの割合にな
るように混合し約3時間攪拌した後、室温にて静置し、
粒子を成長、熟成させた。この後、減圧濃縮することに
より、分散性の良好なシリカ微粒子分散液を調製した。[Example] Ethyl silicate, ethanol, water, aqueous ammonia (2
9%) were mixed in a molar ratio of 1Nia and 6:4:0.0B, stirred for about 3 hours, and left to stand at room temperature.
The particles were grown and aged. Thereafter, by concentrating under reduced pressure, a silica fine particle dispersion with good dispersibility was prepared.
次に、先のエチルシリケートの/4量のエチルシリケー
トを用い、重量比で1;1になるように002規定の塩
酸を加え、氷冷しながら約2時間攪拌することにより加
水分解溶液を調製した。Next, using ethyl silicate in an amount equal to /4 of the amount of ethyl silicate used above, add 002N hydrochloric acid so that the weight ratio is 1:1, and stir for about 2 hours while cooling with ice to prepare a hydrolyzed solution. did.
ここで、前記シリカ微粒子分散液のPH値を2規定の塩
酸を添加し4.5に調整した後、エチルシリケートの加
水分解溶液を混合し、均質な液状ゾルになるまで充分攪
拌した。その後、該液状ゾルに0.2規定のアンモニア
水を滴下し、PH値を5.0に調整し、60X60×1
5crRの箱型容器に72を該ゾルを注入した。更にフ
タをして密閉状態にしてゲル化させウェットゲルを作製
した。この状態にてウェットゲルの線収縮率は7〜8%
程度であり放出した溶媒中に浸漬している状態であった
このようにして得られたウェットゲルを、乾燥容器に移
し入れ、70℃に保持した恒温乾燥機にて乾燥し、はぼ
3週間で乾燥が終了し、46×43X1.5cntの板
状の白色ゲルが得られた。Here, the pH value of the silica fine particle dispersion was adjusted to 4.5 by adding 2N hydrochloric acid, and then a hydrolyzed solution of ethyl silicate was mixed therein and sufficiently stirred until a homogeneous liquid sol was obtained. After that, 0.2N ammonia water was added dropwise to the liquid sol, the pH value was adjusted to 5.0, and 60×60×1
The sol was injected into a 5crR box-shaped container. Furthermore, the container was sealed with a lid to form a gel, thereby producing a wet gel. In this state, the linear shrinkage rate of wet gel is 7 to 8%.
The wet gel thus obtained, which was still immersed in the released solvent, was transferred to a drying container and dried in a constant temperature dryer kept at 70°C for about 3 weeks. The drying was completed and a plate-shaped white gel of 46 x 43 x 1.5 cnt was obtained.
得られた2個のゲル体を酸素/窒素 雰囲気中で一旦9
00℃まで加熱した後、室温まで冷却した後、一方のゲ
ルに対して、あらかじめ調製しておいたエチルシリケー
トの加水分解溶液に5時間浸漬し、70℃にて乾燥した
後、再び、酸素/窒素 雰囲気中で900℃まで加熱し
た。ここで行なった900℃の加熱処理は、ゲルの縮合
反応の促進、脱水、脱有磯残基の各種処理を施すことを
目的とするものである。また、この処理後のゲル体の緻
密化は不充分で多孔性であった。The two gel bodies obtained were once heated in an oxygen/nitrogen atmosphere.
After heating to 00°C and cooling to room temperature, one of the gels was immersed in a previously prepared hydrolysis solution of ethyl silicate for 5 hours, dried at 70°C, and then immersed in oxygen / It was heated to 900°C in a nitrogen atmosphere. The purpose of the heat treatment at 900° C. here is to accelerate the condensation reaction of the gel, dehydrate it, and perform various treatments to remove the residues. Further, the gel body after this treatment was insufficiently densified and was porous.
これら2個のゲル体を、更に減圧下で1350℃まで加
熱し、ガラス化させた後、窒素雰囲気中で1750℃ま
で昇温し、30分間保持した後、徐冷した。These two gel bodies were further heated to 1350° C. under reduced pressure to vitrify, and then heated to 1750° C. in a nitrogen atmosphere, held for 30 minutes, and then slowly cooled.
こうして得られたガラス体は、透明性の高い無色の板状
で、大きさは、およそ50 X 30 X 1.0国で
あった。The glass body thus obtained was a highly transparent, colorless, plate-like material with a size of approximately 50 x 30 x 1.0 mm.
また、得られたガラスの指物性は、密度、熱膨張係数、
赤外および近赤外吸収スペクトルなどほぼ石英ガラスと
一致していた。In addition, the physical properties of the obtained glass include density, coefficient of thermal expansion,
The infrared and near-infrared absorption spectra almost matched those of silica glass.
ところが、3点支持法による曲げ強度測定結果は焼結ゲ
ル体に処理を施したガラスの方が極めて大きな値を示し
た。However, the bending strength measurement results using the three-point support method showed that the glass in which the sintered gel body had been treated had a much larger value.
[発明の効果]
以上のように、不発明の方法によれば、板状ガラスの機
械的強度の向上が容易である。[Effects of the Invention] As described above, according to the uninvented method, it is easy to improve the mechanical strength of sheet glass.
したがって、腕時計のカバーガラス、各種基板をはじめ
、IC用のパッケージなど、高強度を必要とする分野へ
の応用が可能である。Therefore, it can be applied to fields that require high strength, such as watch cover glasses, various substrates, and IC packages.
また、ゾル調製工程において、B、Ti、Ge。In addition, in the sol preparation step, B, Ti, and Ge.
Na、Oa、Li、At、Te、Zr、Os、Nd、O
r など種々の元素をドープすることが可能であり、
強度的に優れた、多種の多成分系ガラスおよび既存組成
にはない新しいガラスの製造も容易である。Na, Oa, Li, At, Te, Zr, Os, Nd, O
It is possible to dope various elements such as r,
It is also easy to produce a variety of multi-component glasses with excellent strength and new glasses that do not have existing compositions.
以上that's all
Claims (1)
るゾル−ゲル法により得られる多孔性の焼結ゲルを、金
属アルコキシドの加水分解溶液に浸漬し、表面付近に拡
散させることを特徴とする板状ガラスの強化方法。At least, a porous sintered gel obtained by a sol-gel method using metal alkoxide or silica particles as a raw material is immersed in a metal alkoxide hydrolysis solution and diffused near the surface. Strengthening method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1962690A JPH03223129A (en) | 1990-01-30 | 1990-01-30 | Method for tempering sheet glass |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1962690A JPH03223129A (en) | 1990-01-30 | 1990-01-30 | Method for tempering sheet glass |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03223129A true JPH03223129A (en) | 1991-10-02 |
Family
ID=12004409
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1962690A Pending JPH03223129A (en) | 1990-01-30 | 1990-01-30 | Method for tempering sheet glass |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03223129A (en) |
-
1990
- 1990-01-30 JP JP1962690A patent/JPH03223129A/en active Pending
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