JPS63147843A - Glass composition - Google Patents
Glass compositionInfo
- Publication number
- JPS63147843A JPS63147843A JP29456386A JP29456386A JPS63147843A JP S63147843 A JPS63147843 A JP S63147843A JP 29456386 A JP29456386 A JP 29456386A JP 29456386 A JP29456386 A JP 29456386A JP S63147843 A JPS63147843 A JP S63147843A
- Authority
- JP
- Japan
- Prior art keywords
- glass
- glass composition
- temperature
- na2o
- chemical durability
- 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
- 239000011521 glass Substances 0.000 title claims abstract description 59
- 239000000203 mixture Substances 0.000 title claims description 25
- 239000000126 substance Substances 0.000 abstract description 20
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 abstract description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 7
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract description 5
- 239000000835 fiber Substances 0.000 abstract description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract description 3
- 239000000377 silicon dioxide Substances 0.000 abstract description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052681 coesite Inorganic materials 0.000 abstract description 2
- 229910052593 corundum Inorganic materials 0.000 abstract description 2
- 229910052906 cristobalite Inorganic materials 0.000 abstract description 2
- 238000000465 moulding Methods 0.000 abstract description 2
- 235000012239 silicon dioxide Nutrition 0.000 abstract description 2
- 229910052682 stishovite Inorganic materials 0.000 abstract description 2
- 229910052905 tridymite Inorganic materials 0.000 abstract description 2
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000007791 liquid phase Substances 0.000 abstract 2
- 238000013329 compounding Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000002994 raw material Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 230000007423 decrease Effects 0.000 description 4
- 239000003365 glass fiber Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004031 devitrification Methods 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N Li2O Inorganic materials [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000003869 coulometry Methods 0.000 description 1
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
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
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はガラス組成物、特に化学的耐久性にすぐれたブ
レイク用及び繊維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, particularly to a glass composition for breakers and fibers having excellent chemical durability.
従来、化学的耐久性にすぐれたガラス繊維はCガラスと
して知られており、その代表的組成は、K、 L、 L
OeWenStein著The Manufactur
ir+gTechnology of Continu
ous Glass Fibers(ELSEVIER
,/ 913年)の31頁の記載によれば、重N% テ
5i026!; + B2O3!;、 AA’2034
’、MgO3+cao IL Na2Ot、!; 、F
e2O30,3である。このCガラスは原料費は安価で
あるが、作業温度(ガラスの粘度が1000ポアズにな
る温度)と液相温度の温度差が50℃以下であり、ガラ
ス組成物は紡糸できるが、ガラス7レイクは失透発生の
ため、製造が困難である。ガラスブレイクは例えば鋼管
内面の摩耗や錆の防止のために、塗料に混入されて鋼管
内面へ塗布されるものであるから当然化学的耐久性が要
求される。従って作業性の良いAガラス(前記LOeW
enSte:Ln Kよれば重重−%で5i0272.
0.Al2O3−2,5,B2O30J、MgO(+、
q、cao 9.0゜Na2O/2.6.に;20 /
−j+Fe2O30,j>からtl造されたガラス7レ
イクは化学的耐久性に乏しく実用的でない。更に火炎延
伸法でガラス短繊維を製造する場合も前記Cガラスは失
透が発生するので、これを用いることができない。Conventionally, glass fiber with excellent chemical durability has been known as C glass, and its typical composition is K, L, L.
The Manufacturer by Oe Wenstein
ir+gTechnology of Continue
ous Glass Fibers (ELSEVIER
, / 913) on page 31, heavy N% Te5i026! ; + B2O3! ;, AA'2034
', MgO3+cao IL Na2Ot,! ; , F
It is e2O30.3. Although the raw material cost of this C glass is low, the temperature difference between the working temperature (the temperature at which the viscosity of the glass becomes 1000 poise) and the liquidus temperature is less than 50°C, and the glass composition can be spun, but is difficult to manufacture due to the occurrence of devitrification. Since glass break is mixed with a paint and applied to the inner surface of a steel pipe to prevent wear and rust on the inner surface of the steel pipe, it is naturally required to have chemical durability. Therefore, A glass with good workability (LOeW)
According to enSte:LnK, weight-% is 5i0272.
0. Al2O3-2,5, B2O30J, MgO(+,
q, cao 9.0°Na2O/2.6. 20 /
-j+Fe2O30,j> glass 7lake has poor chemical durability and is not practical. Further, even when short glass fibers are produced by flame drawing, the C glass cannot be used because devitrification occurs.
Cガラスのもつ作業性の悪さを改良した繊維用ガラス組
成物として米国特許第a、3ii、qs−号に開示され
たガラス組成物は、重量%で5i02!r−62,1)
203/ −、! 、cao r−9,!; 、Mg
O2J−3、!; 、Na2O/j−/7 、に200
−/ 、 B2O3j−7。The glass composition disclosed in U.S. Pat. r-62,1)
203/-,! ,cao r-9,! ; , Mg
O2J-3,! ; , Na2O/j-/7, 200
−/ , B2O3j-7.
Li2O0,/−0,u 、znO/、よ−3,5テあ
ル。コノ組成は、Na2Oを増加させて作業性を改善し
、L120とZnOを加えることによって化学的耐久性
を向上させている。しかしLi2OとZnOは非常に高
価である。Li2O0,/-0,u, znO/, yo-3,5 Teal. The Kono composition improves workability by increasing Na2O, and improves chemical durability by adding L120 and ZnO. However, Li2O and ZnO are very expensive.
以上述べたように安価なCガラスは作業性が劣り、作業
性の良いガラスは高価であって、安価で作業性が良く、
化学的耐久性も充分なガラス組成は従来存在しなかった
と云える。As mentioned above, cheap C glass has poor workability, and glass with good workability is expensive;
It can be said that no glass composition with sufficient chemical durability has hitherto existed.
本発明はこの矛盾を解決して、安価で作業性が良く、化
学的耐久性にすぐれた7レイク用及び繊維用のガラス組
成物を提案するものである。The present invention solves this contradiction and proposes a glass composition for 7 lakes and fibers that is inexpensive, easy to work with, and has excellent chemical durability.
本発明の要旨は電量%で表示して本質的に下記組成
5i02 63.0−67.0B203
’1.,0−1f、1A1203
tl、0−!;、!;TiO20−≠、0
Mg0 、 2.6−3.6CaO
#、7−r、7
BaOO−!;、0
Na20 7.j−/J、9に20
0−λ、0Na20 + K2
OIr、 0−/ r、rFe2O30−/、0
Zr02 0−!;、、0を有す
ることを特徴とするガラス組成物である。The gist of the present invention essentially consists of the following composition expressed in coulometric %: 5i02 63.0-67.0B203
'1. ,0-1f,1A1203
tl, 0-! ;、! ;TiO20-≠, 0 Mg0, 2.6-3.6CaO
#, 7-r, 7 BaOO-! ;, 0 Na20 7. j-/J, 9 to 20
0-λ, 0Na20 + K2
OIr, 0-/ r, rFe2O30-/, 0 Zr02 0-! ; , 0.
良好な作業性を確保するために、該ガラス組成物は、作
業温度が液相温度より/!;O′C以上高いことが好ま
しい。更に好ましくは、高温での成形作業をさけるため
に該ガラス組成物の液相温度は/ O!; O”C以下
である。又該ガラス組成物は化学的耐久性が要求される
ので、耐酸性、耐水性は重量減で表示して7%以下であ
る(試験法は実施例参照)。In order to ensure good workability, the glass composition must have a working temperature of /! below the liquidus temperature. ; It is preferable that it is higher than O'C. More preferably, the liquidus temperature of the glass composition is /O! in order to avoid molding operations at high temperatures. ; O''C or less. Also, since the glass composition is required to have chemical durability, the acid resistance and water resistance are 7% or less expressed as weight loss (see Examples for the test method).
本発明の組成限定理由は次の通りである。 The reasons for limiting the composition of the present invention are as follows.
5102はB2O3r Al 203と共にガラスの骨
格を形成する。5i02の1が67.0%をこえると、
ガラスの溶解性が低下するとともに、ガラスの作業rM
度、液相温度が上昇して好ましくない。SiO2の石が
63.0%未満ではガラスの化学的耐久性が低下して好
ましくない。5102 forms a glass skeleton together with B2O3r Al 203. When 1 of 5i02 exceeds 67.0%,
As the solubility of the glass decreases, the working rM of the glass
degree, the liquidus temperature increases, which is undesirable. If the SiO2 stone content is less than 63.0%, the chemical durability of the glass will deteriorate, which is not preferable.
B2O3は<z、、r%をこえると、ガラスの原料費の
増加をまねき、かつガラスの作業温度と液相温度の湿度
差が小さくなり、好ましくない。B2O3がグ、O%未
満では、ガラスの粘性が塔太し、作業温度、液相温度が
上昇して好ましくない。When B2O3 exceeds <z, r%, it is not preferable because it increases the raw material cost of the glass and reduces the humidity difference between the working temperature and the liquidus temperature of the glass. If B2O3 is less than 0%, the viscosity of the glass increases and the working temperature and liquidus temperature increase, which is undesirable.
Al2O3はガラスの化学的耐久性、特に耐水性を向上
させるので必須成分であるが、j、5%をこえても耐水
性を向上させる効果がないので5.5%を上限とし、1
).0%未満では耐水性が低下するのでψ、O%を下限
とする。Al2O3 is an essential component because it improves the chemical durability of glass, especially water resistance, but it has no effect on improving water resistance even if it exceeds 5%, so 5.5% is the upper limit, and 1
). If it is less than 0%, the water resistance decreases, so ψ, O% is set as the lower limit.
TlO2は化学的耐久性を向上させる成分であるが、原
料が高価であるので使用しない方が好ましい。使用する
場合でちび、0%をこえても化学的)、。Although TlO2 is a component that improves chemical durability, it is preferable not to use it because the raw material is expensive. When used, it is chemical even if it exceeds 0%).
久性向上の効果はないのでダ、O%を上限とする。Since there is no effect of improving durability, the upper limit is set at 0.0%.
MgOとCaOはガラスの融剤である。同時にこれらは
ガラスの粘度曲線を適切に保つために組み合わせて使用
され、更に化学的耐久性を維持するためにも使用される
。MgOは本発明においてはjJ〜3.6%の範囲で液
f@湿温度下げるので、この範囲に限定する。CaOは
L7%をこえると液相温度を高めるので好ましくない。MgO and CaO are fluxing agents for glass. At the same time, they are used in combination to keep the viscosity curve of the glass appropriate and also to maintain chemical durability. In the present invention, since MgO lowers the liquid f@humidity temperature within the range of jJ to 3.6%, it is limited to this range. CaO is not preferable if it exceeds L7% because it increases the liquidus temperature.
L7%未満では化学的耐久性を低下させるので好ましく
ない。If L is less than 7%, it is not preferable because it lowers chemical durability.
BaOは化学的耐久性を低下させることなく、融剤とし
て作用し、又液相温度を下げる成分である。BaO is a component that acts as a fluxing agent and lowers the liquidus temperature without reducing chemical durability.
しかし原料が比較的高価であるので使用しないのが好ま
しい。BaOを使用する場合もLO%をこえると液相温
度を下げる効果が小さくなるので5.0%を上限とする
。However, since the raw materials are relatively expensive, it is preferable not to use it. Even when BaO is used, if it exceeds LO%, the effect of lowering the liquidus temperature becomes small, so the upper limit is set at 5.0%.
Na2Oとに20はガラスの融剤である。Na2Oにく
らべに20は原料が高価であるのでNa2Oを主成分と
して用いるのが好ましい。Na2O and 20 are glass fluxing agents. Since 20 is a more expensive raw material than Na2O, it is preferable to use Na2O as the main component.
Na2Oが13.9%をこえるとガラスの化学的耐久性
が低下するのでNa2Oは13.9%を上限とする。If Na2O exceeds 13.9%, the chemical durability of the glass decreases, so the upper limit of Na2O is 13.9%.
Na2Oが74%未満では、ガラスの溶解性が低下し、
同時に液相温度も上昇するので好ましくない。When Na2O is less than 74%, the solubility of the glass decreases,
At the same time, the liquidus temperature also increases, which is not preferable.
従ってNa2Oは7.5%を下限とする。K2Oはガラ
ス原料として特別に調合する必要はないが、珪砂、長石
などに20以外の成分を導入するために用いられる原料
から混入する場合があるので、2.0%を上限とする。Therefore, the lower limit of Na2O is set at 7.5%. K2O does not need to be specially prepared as a glass raw material, but it may be mixed in from raw materials used to introduce components other than 20 into silica sand, feldspar, etc., so the upper limit is set at 2.0%.
Na2Oと置換してに20を導入していけば、混合アル
カリ効果により化学的耐久性が向上することは公知であ
るが、本発明の主U艮とするところは、安価なガラス組
成分を提案することにあるので、この点からもに20は
2.0%が上限である。尚Na、20 十に20は、N
a 20の項で述べたのとまったく同じ理由から、上限
を/jJ%、下限をざ、0%とする。It is known that chemical durability can be improved by the mixed alkali effect if 20 is introduced in place of Na2O, but the main aim of the present invention is to propose an inexpensive glass composition. Therefore, from this point of view, the upper limit for 20 is 2.0%. Furthermore, Na, 20 20 in ten is N
For exactly the same reason as stated in section 20, the upper limit is set to /jJ% and the lower limit is set to 0%.
Fe2O3は必須成分ではないが、ガラス原料中の不純
物として混入されるので/、0%を上限とする。Although Fe2O3 is not an essential component, it is mixed as an impurity in the glass raw material, so the upper limit is set at 0%.
zro2は化学的耐久性を高める成分であるが、多fi
K用いると、ガラスの粘度を高め、溶解性を低下させる
ので、3.0%を上限とする。ZRO2 is a component that increases chemical durability, but it
When K is used, it increases the viscosity of the glass and reduces the solubility, so the upper limit is set at 3.0%.
以上に、ガラス成分の作用を述べたが、特に化学的耐久
性が重視される場合は、TlO2,ZrO2をそれぞれ
q、0重量%およびj、O重量%までのf用いることが
好ましい。本発明の組成物は以上に述べた成分の合計を
すくなくとも95重重量含有する。すなわち仲の成分と
してZnOを多くとも7重量%、SrOを多くとも7重
量%、PbOを多くとも/重量%など、W!量酸成分し
てAS203を多くともO,S重量%、5b203を多
くとも0.5重量%などが含まれていてもよい。The effects of the glass components have been described above, but when chemical durability is particularly important, it is preferable to use TlO2 and ZrO2 in amounts up to q and 0% by weight and j and 0% by weight, respectively. The composition of the present invention contains at least 95% by weight of the above-mentioned ingredients. That is, ZnO as a middle component is at most 7% by weight, SrO is at most 7% by weight, PbO is at most /% by weight, etc., W! As acid components, AS203 may be contained in an amount of at most O, S, and 5b203 may be contained in an amount of at most 0.5 weight %.
次に本発明の実施例について説明する。第1表の組成(
重量%)を有する硝子を溶融して作業温度、液相温度、
耐水性、耐酸性を測定した。その結果を第1表に示す。Next, examples of the present invention will be described. Composition in Table 1 (
(wt%) by melting glass with working temperature, liquidus temperature,
Water resistance and acid resistance were measured. The results are shown in Table 1.
液相温度は次のよう圧して辿]定した。The liquidus temperature was determined by pressure as follows.
ガラスを粉砕して1610μm のフルイを通り//9
0μm のフルイ上にとどまったガラス粒を、アルコー
ルに浸仏して超音波をp)はて洗滌し、恒占劣で乾燥さ
せた。このガラス粒を白金ボート上に7列にあけた/
in径の多数の穴の上シでボート長さ方向に適当な温度
勾配をもつように温度設定された炉中で4時間保持する
。′炉から取量した白金ポート上のガラス粒を観察し、
失透が発生している最高温度をもって液相温度とした。Crush the glass and pass it through a 1610μm sieve //9
The glass particles remaining on the 0 μm sieve were immersed in alcohol, washed with ultrasonic waves, and dried under constant pressure. These glass grains were placed in seven rows on a platinum boat.
The boat was held for 4 hours in a furnace whose temperature was set to have an appropriate temperature gradient in the lengthwise direction of the boat at the top of a number of holes with a diameter of 1.5 inch. 'Observe the glass particles on the platinum port taken from the furnace,
The highest temperature at which devitrification occurred was defined as the liquidus temperature.
耐水性の1)1定は次のようにした。ガラスを紡糸用の
白金ポットに入れて直径9μmのガラス繊維を紡糸する
。ガラスIFi維を約30開の長さに切ったものを、約
2gとり、デシケータ中で一ダ時間保持して乾燥する。1) One constant of water resistance was determined as follows. Glass is placed in a spinning platinum pot and glass fibers with a diameter of 9 μm are spun. Approximately 2 g of glass IFi fiber cut into approximately 30 mm length is taken and kept in a desiccator for one hour to dry.
この試料の重量をo、/mmgの単位迄精秤する。次K
M料をパイレックスガラス製のビーカーに入れ、蒸留水
を200m1入れる。このビーカーをto”cに保持さ
れた恒温摺に入れてS時間保持する。この間、適宜ビー
カーを振とつする。The weight of this sample is precisely weighed to the nearest o./mmg. Next K
Put the M material into a Pyrex glass beaker and add 200ml of distilled water. This beaker is placed in a constant temperature slide held at to''c and held for S time. During this time, the beaker is shaken as appropriate.
この液をガラスフィルターで瀞過し、試料を蒸留水で洗
滌する。試料を十分乾燥した後その重■を0、Immg
迄精秤する。最初の試料重滑に対する、試験後の試料の
重量減を重量%で表示して耐水性とする。This liquid is filtered through a glass filter, and the sample is washed with distilled water. After thoroughly drying the sample, its weight is reduced to 0, Immg.
Weigh accurately. The weight loss of the sample after the test with respect to the initial weight of the sample is expressed in weight% and is defined as water resistance.
耐酸性の測定は、耐水性の測定に4しる。耐水性試験で
蒸留水を用いたかわりに比重/200の希硫酸を200
m1用いる。Measurement of acid resistance is classified as 4 in the measurement of water resistance. Instead of using distilled water in the water resistance test, dilute sulfuric acid with a specific gravity of 200
Use m1.
上記実施例かられかるように、耐水性、耐酸性にすぐれ
、作業温度と液相温度の差がiso”c以上たとえば/
1,0〜300℃であって、作業性にすぐれた。しかも
比較的安価がガラス組成物を得ることができる。As can be seen from the above examples, it has excellent water resistance and acid resistance, and the difference between working temperature and liquidus temperature is more than iso"c, for example / /
The temperature was 1.0 to 300°C, and the workability was excellent. Furthermore, a glass composition can be obtained at a relatively low cost.
第 l 表Table 1
Claims (3)
であることを特徴とするガラス組成物。(1) The following components expressed in weight%: SiO_2 63.0-67.0 B_2O_3 4.0-4.8 Al_2O_3 4.0-5.5 TiO_2 0-4.0 MgO 2.5-3.6 CaO 4.7-8.7 BaO 0-5.0 Na_2O 7.5-13.9 K_2O 0-2.0 Na_2O+K_2O 8.0-15.5 Fe_2O_3 0-1.0 ZrO_2 0-5.0 , the sum of these components is at least 95% by weight
A glass composition characterized by:
とも150℃高い作業温度(ガラス組成物の粘度が10
00ポアズになる温度)を有するものである特許請求の
範囲第1項記載のガラス組成物。(2) The glass composition has a working temperature at least 150°C higher than its liquidus temperature (the viscosity of the glass composition is 10°C).
The glass composition according to claim 1, wherein the glass composition has a temperature of 0.00 poise.
度と、その液相温度よりも160〜300℃高い作業温
度を有するものである特許請求の範囲第2項記載のガラ
ス組成物。(3) The glass composition according to claim 2, wherein the glass composition has a liquidus temperature of at most 1050°C and a working temperature 160 to 300°C higher than the liquidus temperature.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29456386A JPS63147843A (en) | 1986-12-10 | 1986-12-10 | Glass composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29456386A JPS63147843A (en) | 1986-12-10 | 1986-12-10 | Glass composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63147843A true JPS63147843A (en) | 1988-06-20 |
JPH0461820B2 JPH0461820B2 (en) | 1992-10-02 |
Family
ID=17809406
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29456386A Granted JPS63147843A (en) | 1986-12-10 | 1986-12-10 | Glass composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63147843A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09110453A (en) * | 1995-10-25 | 1997-04-28 | Nippon Glass Fiber Co Ltd | Alkali-resistant glass flake and thermoplastic resin composition or thermosetting resin composition reinforced with the flake |
JP2002110124A (en) * | 2000-09-28 | 2002-04-12 | Nippon Muki Co Ltd | Separator for sealed lead-acid battery |
WO2002030843A1 (en) * | 2000-10-11 | 2002-04-18 | Paramount Glass Manufacturing Co., Ltd. | Glass composition for production of inorganic fibers and products of forming thereof |
WO2008111602A1 (en) * | 2007-03-15 | 2008-09-18 | Nippon Electric Glass Co., Ltd. | Glass composition for glass fiber, glass fiber, process for producing glass fiber and composite material |
FR2922885A1 (en) * | 2007-10-31 | 2009-05-01 | Saint Gobain Technical Fabrics | GLASS YARNS WITH A LOW ALUMINUM CONTENT FOR STRENGTHENING ORGANIC AND / OR INORGANIC MATERIALS. |
US8461070B2 (en) | 2007-03-28 | 2013-06-11 | Pilkington Group Limited | Glass composition |
JP5629579B2 (en) * | 2008-08-27 | 2014-11-19 | 日本板硝子株式会社 | Scale glass and coated scale glass |
WO2016151322A1 (en) * | 2015-03-26 | 2016-09-29 | Pilkington Group Limited | Novel glasses |
WO2016151325A1 (en) * | 2015-03-26 | 2016-09-29 | Pilkington Group Limited | Glasses |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50145411A (en) * | 1974-05-14 | 1975-11-21 |
-
1986
- 1986-12-10 JP JP29456386A patent/JPS63147843A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50145411A (en) * | 1974-05-14 | 1975-11-21 |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09110453A (en) * | 1995-10-25 | 1997-04-28 | Nippon Glass Fiber Co Ltd | Alkali-resistant glass flake and thermoplastic resin composition or thermosetting resin composition reinforced with the flake |
JP2002110124A (en) * | 2000-09-28 | 2002-04-12 | Nippon Muki Co Ltd | Separator for sealed lead-acid battery |
WO2002030843A1 (en) * | 2000-10-11 | 2002-04-18 | Paramount Glass Manufacturing Co., Ltd. | Glass composition for production of inorganic fibers and products of forming thereof |
WO2008111602A1 (en) * | 2007-03-15 | 2008-09-18 | Nippon Electric Glass Co., Ltd. | Glass composition for glass fiber, glass fiber, process for producing glass fiber and composite material |
US8461070B2 (en) | 2007-03-28 | 2013-06-11 | Pilkington Group Limited | Glass composition |
FR2922885A1 (en) * | 2007-10-31 | 2009-05-01 | Saint Gobain Technical Fabrics | GLASS YARNS WITH A LOW ALUMINUM CONTENT FOR STRENGTHENING ORGANIC AND / OR INORGANIC MATERIALS. |
WO2009056768A3 (en) * | 2007-10-31 | 2009-06-25 | Saint Gobain Technical Fabrics | Low alumina content glass yarns for reinforcing organic and/or inorganic materials |
US8367571B2 (en) | 2007-10-31 | 2013-02-05 | Saint-Gobain Technical Fabrics Europe | Glass strands with low alumina content capable of reinforcing organic and/or inorganic materials |
JP5629579B2 (en) * | 2008-08-27 | 2014-11-19 | 日本板硝子株式会社 | Scale glass and coated scale glass |
US9237994B2 (en) | 2008-08-27 | 2016-01-19 | Nippon Sheet Glass Company, Limited | Glass flake and coated glass flake |
WO2016151322A1 (en) * | 2015-03-26 | 2016-09-29 | Pilkington Group Limited | Novel glasses |
WO2016151325A1 (en) * | 2015-03-26 | 2016-09-29 | Pilkington Group Limited | Glasses |
CN107531548A (en) * | 2015-03-26 | 2018-01-02 | 皮尔金顿集团有限公司 | New glass |
JP2018510835A (en) * | 2015-03-26 | 2018-04-19 | ピルキントン グループ リミテッド | New glass |
US20180118607A1 (en) * | 2015-03-26 | 2018-05-03 | Pilkington Group Limited | Novel glasses |
US10683231B2 (en) | 2015-03-26 | 2020-06-16 | Pilkington Group Limited | Glasses |
Also Published As
Publication number | Publication date |
---|---|
JPH0461820B2 (en) | 1992-10-02 |
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