JPS61101433A - Glass composition for chemical reinforcing - Google Patents
Glass composition for chemical reinforcingInfo
- Publication number
- JPS61101433A JPS61101433A JP22079684A JP22079684A JPS61101433A JP S61101433 A JPS61101433 A JP S61101433A JP 22079684 A JP22079684 A JP 22079684A JP 22079684 A JP22079684 A JP 22079684A JP S61101433 A JPS61101433 A JP S61101433A
- Authority
- JP
- Japan
- Prior art keywords
- glass
- glass composition
- mgo
- al2o3
- zno
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
- C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
- C03C3/093—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Surface Treatment Of Glass (AREA)
- Glass Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はイオン交換による化学強化用ガラス組成物に関
する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a glass composition for chemical strengthening by ion exchange.
ガラスを歪点以下の温度のアルカリ金属イオンを含む溶
融塩中に浸漬し、ガラス中のアルカリ金属イオンを溶融
塩中のより原子半径の大きいアルカリ金属イオンと交換
させてガラス表面に圧縮応力を生せしめる謂る化学強化
法は古くから知られている。さらに用いられるアルカリ
金属イオンとして、ガラス中のHa+を溶融塩中のに+
に交換することはS、 S、 K15tler (J、
Amer、 Ceram、 Soc。Glass is immersed in a molten salt containing alkali metal ions at a temperature below the strain point, and the alkali metal ions in the glass are exchanged with alkali metal ions with a larger atomic radius in the molten salt, producing compressive stress on the glass surface. The so-called chemical strengthening method has been known for a long time. Further, as the alkali metal ions used, Ha+ in the glass is converted into Ha+ in the molten salt.
Replacement with S, S, K15tler (J,
Amer, Ceram, Soc.
VOl、l)に発表されている。そしてガラス中でのに
+の拡散速度を早めるためにガラスにAJ203又はz
ro2を含有せしめることはCOrning社の特許(
例えば持分W3 tI/−201,29、特公昭l!7
−弘7970 、特公昭1−//327等)に記載され
ている。しかしAl2O3又はZrO2を多く含むガラ
スは溶融温度や成形温度が高いという欠点を有する。VOl, l). Then, in order to speed up the diffusion rate of + in the glass, AJ203 or z was added to the glass.
The inclusion of ro2 is a patent of Corning (
For example, equity W3 tI/-201,29, Tokuko Sho I! 7
- Hiroshi 7970, Tokuko Sho 1-//327, etc.). However, glasses containing a large amount of Al2O3 or ZrO2 have the disadvantage of high melting and forming temperatures.
ガラスの溶融性を向上させかつに+の拡散速度5iO2
69〜7I1%、Na2O5〜13%p K20 A=
/ 2%。Improving the meltability of glass and increasing the diffusion rate of +5iO2
69-7I1%, Na2O5-13%p K20 A=
/ 2%.
Na2O十に20 /J 〜/9%、1203 ’4%
以下、 Zr02II%以下、 Al2O3+ZrO2
2〜7%、MgO10%以下。Na2O 20/J~/9%, 1203'4%
Below, Zr02II% or less, Al2O3+ZrO2
2-7%, MgO 10% or less.
ZnOs%以下、 MgO+ZnO2ヘ/、2% 、B
2O311%以下。ZnOs% or less, MgO+ZnO2/, 2%, B
2O3 11% or less.
5i02+Na2O+に20+Ajl’203+ZrO
2+MgO+ZnO十B2O394%以上からなる。し
かしながらこの組成のガラスでも依然溶融湿度が高く、
ガラスの粘性がto2gイズで定義される溶融点は1s
oo℃以上である。5i02+Na2O+ to 20+Ajl'203+ZrO
It consists of 2+MgO+ZnO+B2O394% or more. However, even with this composition, the melting humidity is still high,
The melting point defined by the viscosity of glass as to2g is 1s
It is 0°C or higher.
本発明はイオン交換時におけるに+の拡散速度が大きく
かつ溶融点が1!;00℃以下の溶融性及び成形性に優
れた化学強化用ガラス組成を提供することを課題とする
。The present invention has a high diffusion rate of + during ion exchange and a melting point of 1! An object of the present invention is to provide a glass composition for chemical strengthening that has excellent meltability and formability at temperatures below 00°C.
前記課雇を解決するため、本発明のガラス組成は重量%
で表示した基本成分が次記範囲にある。In order to solve the above problems, the glass composition of the present invention is
The basic components indicated by are within the following range.
5i02 60〜72
B2o3j〜l0
A12033〜6 (但しAz2o3+zro2 J
〜4)MgO!r〜10
zno o〜 6
Li20 0−2
Na20 J 〜/4’
に20 3へ 6
〔作 用〕
5i02 ニガラス骨格を形成する主要成分であり、
60%未満ではガラスが化学的に不安定で耐水性や耐酸
性などに乏しくなり、72%を越えると溶融温度が高く
なる。5i02 60~72 B2o3j~l0 A12033~6 (However, Az2o3+zro2 J
~4) MgO! r~10 zno o~ 6 Li20 0-2 Na20 J ~/4' to 20 3 6 [Function] 5i02 Main component forming the Nigarasu skeleton,
When it is less than 60%, the glass becomes chemically unstable and has poor water resistance and acid resistance, and when it exceeds 72%, its melting temperature becomes high.
B2O3ニガラス骨格を形成するとともにガラスの溶融
温度、成形温度を低下せしめるが1.t%未満では溶融
温度低下の効果が乏しくなり、10%を越えると溶融、
成形時にB2O3が揮発しやすく、組成変動によって脈
理や失透などの欠点が生じ易くなる。B2O3 forms a glass skeleton and lowers the melting temperature and molding temperature of the glass, but 1. If it is less than t%, the effect of lowering the melting temperature will be poor, and if it exceeds 10%, it will melt,
B2O3 tends to volatilize during molding, and defects such as striae and devitrification are likely to occur due to compositional fluctuations.
AA203 ニガラスを化学的に安定にするとともに、
Na十#に+のイオン交換を促進する。3%未満ではイ
オン交換促進の効果が小さく、6%を越えるとガラスの
溶融温度が高くなり、かつガラスが失透しやすくなる。AA203 In addition to making Nigaras chemically stable,
Promotes ion exchange of + to Na+. If it is less than 3%, the effect of promoting ion exchange will be small, and if it exceeds 6%, the melting temperature of the glass will be high and the glass will be prone to devitrification.
なおzro2もAl2O3と同じ作用を果すのでAl2
O3+ZrO2の範囲も3〜6%とする。Note that zro2 also has the same effect as Al2O3, so Al2
The range of O3+ZrO2 is also 3 to 6%.
MgO:に+のガラス中での拡散速度を減じることなく
ガラスの高温での粘性を低下させガラスを溶しやすくす
る。5%未満ではその効果に乏しく、10%を越えると
ガラスが失透しやすくなる。MgO: Reduces the viscosity of the glass at high temperatures without reducing the diffusion rate in the glass, making it easier to melt the glass. If it is less than 5%, the effect is poor, and if it exceeds 10%, the glass tends to devitrify.
ZnOj MgOと同様ガラスの溶融性を向上させるが
、本願ではB2O3とMgOの添加によって溶融性が改
良されているので必須ではない。しかし還元性雰囲気に
おいて溶融ガラス中に溶解しているSO3が還元されて
アンバー着色を起す様な条件下ではガラス中にznOが
存在すると還元されたSを無色のZnSとして固定しア
ンバー着色を防ぐので、2%以上含有するのが好ましい
。ZnOj Improves the meltability of glass like MgO, but is not essential in this application because the meltability is improved by the addition of B2O3 and MgO. However, under conditions where SO3 dissolved in molten glass is reduced in a reducing atmosphere and causes amber coloration, the presence of ZnO in the glass fixes the reduced S as colorless ZnS and prevents amber coloration. , preferably 2% or more.
例えば70−トバスを用いてガラスを板状に成形する場
合、8分を含んだガラスはアンバー着色を起しやすいが
、ガラス中にZnOを2%以上含ませておけば防ぐこと
ができる。しかしZnOはガラスの温粘曲線を急勾配に
して成形性を悪くする欠点もあるので4%を越えてはな
らない。For example, when glass is formed into a plate shape using 70-Tobath, glass containing 8% is likely to cause amber coloring, but this can be prevented by containing 2% or more of ZnO in the glass. However, ZnO has the disadvantage of making the temperature-viscosity curve of the glass steeper, thereby impairing formability, so its content should not exceed 4%.
Li2Oニガラスの溶融性を向上させるので0.3%程
度含有するのが好ましいが、原料が高価であるので必須
ではない。また2%を越えても溶融性向上の効果はない
ので2%を上限とする。It is preferable to contain about 0.3% since it improves the meltability of Li2O Nigarasu, but it is not essential since the raw material is expensive. Moreover, since there is no effect of improving meltability even if the content exceeds 2%, the upper limit is set at 2%.
Na2O:に+とイオン交換してガラス表層部に所要の
圧縮応力を生ぜしめるのに4%は必要である。Na2O: 4% is necessary for ion exchange with + to produce the required compressive stress in the glass surface layer.
しかしlψ%を越えるとガラスの化学的耐久性を低下さ
せる。However, if it exceeds lψ%, the chemical durability of the glass decreases.
K2O: Na2Oと共存することによりに+の拡散を
促進させるので少くとも3%は必要である。しかし6%
を越えるとガラス中のアルカリ金成分が多くなりすぎ、
ガラスの化学的耐久性を低下させる。K2O: Coexists with Na2O to promote + diffusion, so at least 3% is required. But 6%
If it exceeds , the alkali gold component in the glass becomes too large,
Reduces the chemical durability of glass.
・ 以上の成分の他に本発明の主旨を害わない範囲で清
澄剤(例えばAS203ySb203.Se3.C1,
F等)、着色剤(例えばNi0,000.Se、MnO
211Ja2o3 +Pr601、等)や不純物を含有
しても構わない。- In addition to the above components, clarifiers (e.g. AS203ySb203.Se3.C1,
F, etc.), colorants (e.g. Ni0,000.Se, MnO
211Ja2o3 +Pr601, etc.) or impurities may be contained.
第1表の組成となるようガラス原料を調合し、白金ルツ
ボ中で溶融し、型枠に鋳込み徐冷して試料を得た。試料
ガラスをKNO3溶融塩に20時間浸漬して化学強化処
理した後表面圧縮応力値を測定した。一方ガラスの溶融
性の目安として溶融点(ガラスの粘性が102ボイズの
温度)および作業点(ガラスの粘性が10’ボイズの温
度)を測定した。Glass raw materials were prepared to have the composition shown in Table 1, melted in a platinum crucible, cast into a mold, and slowly cooled to obtain a sample. After chemically strengthening the sample glass by immersing it in KNO3 molten salt for 20 hours, the surface compressive stress value was measured. On the other hand, as a measure of the meltability of the glass, the melting point (temperature at which the viscosity of the glass is 102 voids) and working point (the temperature at which the viscosity of the glass is 10' voids) was measured.
結果を第1表に記す。The results are shown in Table 1.
第1表実施例番号/−4は本発明のガラス組成範囲内の
ガラスで、実施例番号7〜りは範囲外のガラスである。Example numbers /-4 in Table 1 are glasses within the glass composition range of the present invention, and Example numbers 7 to 2 are glasses outside the range.
実施例番号/−4のガラスはいずれも高い表面圧縮応力
を持ちかつ溶融点が1600°Cを大巾に下廻っている
が、実施例番号7のガラスはA6203 +zro2が
9j%もあるため、実施例番号ざ、りのガラスはB2O
3又はMgOが少いので溶融点が/jtoq″C以上で
ありかつ作業点も本発明組成i凹円のガラスに較べて高
い。The glasses of Example No./-4 all have high surface compressive stress and the melting point is well below 1600°C, but the glass of Example No. 7 has A6203 + zro2 of 9j%, so it is difficult to carry out the implementation. Example number Zaori's glass is B2O
Since the amount of 3 or MgO is small, the melting point is higher than /jtoq''C, and the working point is also higher than the concave glass of the composition i of the present invention.
本発明のガラスは従来のガラスに較べて化学強化処理に
よって高い強度を発現するとともに、溶融点・作業点が
低いので溶融・成形が容易である。The glass of the present invention exhibits higher strength than conventional glasses through chemical strengthening treatment, and has a lower melting point and working point, making it easier to melt and mold.
IRI−IRI-
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22079684A JPS61101433A (en) | 1984-10-20 | 1984-10-20 | Glass composition for chemical reinforcing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22079684A JPS61101433A (en) | 1984-10-20 | 1984-10-20 | Glass composition for chemical reinforcing |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61101433A true JPS61101433A (en) | 1986-05-20 |
JPH0444612B2 JPH0444612B2 (en) | 1992-07-22 |
Family
ID=16756698
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP22079684A Granted JPS61101433A (en) | 1984-10-20 | 1984-10-20 | Glass composition for chemical reinforcing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61101433A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63175220A (en) * | 1987-01-16 | 1988-07-19 | Tdk Corp | Magnetic recording medium |
FR2761978A1 (en) * | 1997-04-11 | 1998-10-16 | Saint Gobain Vitrage | GLASS COMPOSITION AND CHEMICALLY TEMPERED GLASS SUBSTRATE |
WO2002051764A3 (en) * | 2000-12-22 | 2002-11-07 | Schott Glas | Borosilicate glass containing zinc oxide |
JP2011088763A (en) * | 2009-10-20 | 2011-05-06 | Asahi Glass Co Ltd | Glass sheet for display, sheet glass for display and method for manufacturing the same |
JP2013121910A (en) * | 2007-03-02 | 2013-06-20 | Nippon Electric Glass Co Ltd | Reinforced plate glass and its manufacturing method |
WO2014005406A1 (en) * | 2012-07-03 | 2014-01-09 | 华南理工大学 | Lead-free fusible green and environment-friendly glass and preparation method thereof |
JP2015054794A (en) * | 2013-09-11 | 2015-03-23 | Hoya株式会社 | Glass for magnetic recording medium substrate and magnetic recording medium substrate |
JP2018528116A (en) * | 2015-07-17 | 2018-09-27 | エージーシー グラス ユーロップAgc Glass Europe | Central console for vehicles |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4939897A (en) * | 1972-08-26 | 1974-04-13 |
-
1984
- 1984-10-20 JP JP22079684A patent/JPS61101433A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4939897A (en) * | 1972-08-26 | 1974-04-13 |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63175220A (en) * | 1987-01-16 | 1988-07-19 | Tdk Corp | Magnetic recording medium |
FR2761978A1 (en) * | 1997-04-11 | 1998-10-16 | Saint Gobain Vitrage | GLASS COMPOSITION AND CHEMICALLY TEMPERED GLASS SUBSTRATE |
WO1998046537A1 (en) * | 1997-04-11 | 1998-10-22 | Saint-Gobain Vitrage | Glass composition and chemically tempered glass substrate |
US6333285B1 (en) | 1997-04-11 | 2001-12-25 | Saint-Gobain Vitrage | Glass composition and chemically tempered glass substrate |
WO2002051764A3 (en) * | 2000-12-22 | 2002-11-07 | Schott Glas | Borosilicate glass containing zinc oxide |
JP2013121910A (en) * | 2007-03-02 | 2013-06-20 | Nippon Electric Glass Co Ltd | Reinforced plate glass and its manufacturing method |
JP2011088763A (en) * | 2009-10-20 | 2011-05-06 | Asahi Glass Co Ltd | Glass sheet for display, sheet glass for display and method for manufacturing the same |
WO2014005406A1 (en) * | 2012-07-03 | 2014-01-09 | 华南理工大学 | Lead-free fusible green and environment-friendly glass and preparation method thereof |
JP2015054794A (en) * | 2013-09-11 | 2015-03-23 | Hoya株式会社 | Glass for magnetic recording medium substrate and magnetic recording medium substrate |
JP2018528116A (en) * | 2015-07-17 | 2018-09-27 | エージーシー グラス ユーロップAgc Glass Europe | Central console for vehicles |
Also Published As
Publication number | Publication date |
---|---|
JPH0444612B2 (en) | 1992-07-22 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |