JPH035343A - Fiberglass composition - Google Patents
Fiberglass compositionInfo
- Publication number
- JPH035343A JPH035343A JP13698489A JP13698489A JPH035343A JP H035343 A JPH035343 A JP H035343A JP 13698489 A JP13698489 A JP 13698489A JP 13698489 A JP13698489 A JP 13698489A JP H035343 A JPH035343 A JP H035343A
- Authority
- JP
- Japan
- Prior art keywords
- cao
- tensile strength
- mgo
- melting
- content
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 13
- 239000011152 fibreglass Substances 0.000 title claims abstract description 7
- 239000000835 fiber Substances 0.000 abstract description 17
- 238000002844 melting Methods 0.000 abstract description 12
- 230000008018 melting Effects 0.000 abstract description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 10
- 239000011521 glass Substances 0.000 abstract description 7
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum oxide Inorganic materials [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 abstract description 5
- 229910052761 rare earth metal Inorganic materials 0.000 abstract description 5
- 239000000377 silicon dioxide Substances 0.000 abstract description 4
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 abstract description 4
- KTUFCUMIWABKDW-UHFFFAOYSA-N oxo(oxolanthaniooxy)lanthanum Chemical compound O=[La]O[La]=O KTUFCUMIWABKDW-UHFFFAOYSA-N 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 4
- 229910052593 corundum Inorganic materials 0.000 abstract 4
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 4
- 229910052681 coesite Inorganic materials 0.000 abstract 3
- 229910052906 cristobalite Inorganic materials 0.000 abstract 3
- 235000012239 silicon dioxide Nutrition 0.000 abstract 3
- 229910052682 stishovite Inorganic materials 0.000 abstract 3
- 229910052905 tridymite Inorganic materials 0.000 abstract 3
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 abstract 2
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 abstract 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 abstract 1
- 239000013078 crystal Substances 0.000 abstract 1
- 239000006023 eutectic alloy Substances 0.000 abstract 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 238000009987 spinning Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000002131 composite material Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 150000002910 rare earth metals Chemical class 0.000 description 2
- 239000012779 reinforcing material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 101100055113 Caenorhabditis elegans aho-3 gene Proteins 0.000 description 1
- 101100348017 Drosophila melanogaster Nazo gene Proteins 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000006060 molten glass Substances 0.000 description 1
- 239000000075 oxide glass Substances 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- PXXKQOPKNFECSZ-UHFFFAOYSA-N platinum rhodium Chemical compound [Rh].[Pt] PXXKQOPKNFECSZ-UHFFFAOYSA-N 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000005303 weighing 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
- C03C13/00—Fibre or filament compositions
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)
- Glass Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は引張強度に優れたファイバーガラス組成物に関
する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a fiberglass composition with excellent tensile strength.
従来ファイバーガラスは複合材料の補強材等として広(
使用されている。公知のEガラスファイバーは引張強度
が280kg/mm”と−船釣な複合材料用補強材とし
て優れているが、高張力を必要とし、あるいは急激に張
力のかかるベルトプーリー、タイミングベルト等におい
ては強度が不充分である。Conventionally, fiberglass has been widely used as a reinforcing material for composite materials (
It is used. The well-known E-glass fiber has a tensile strength of 280 kg/mm" and is excellent as a reinforcing material for composite materials used in boat fishing. However, it is not strong enough for belt pulleys, timing belts, etc. that require high tension or are subject to sudden tension. is insufficient.
酸化物ガラスファイバーにおいては、分子結合エネルギ
ー等から想定すれば500 kg/mm2以上に達する
ものと推定され、したがって、これに近い抗張力でかつ
実用性のあるガラスファイバーの開発が急務とされてい
る。In oxide glass fibers, it is estimated to reach 500 kg/mm2 or more based on molecular bond energy, etc. Therefore, there is an urgent need to develop a practical glass fiber with a tensile strength close to this.
前記Eガラスに代わるものとしてはSiO□65重量%
(以下単に%という)、AIZO:l 25%、MgO
10%で代表される(通称Sガラス)イギリスパテント
第1209244号における開示組成物、あるいは5i
Oz 60χ、AIZO325%、MgO6%、CaO
9%で代表される(通称Rガラス)フランスパテント第
1435073号における開示組成物等があり、前記E
ガラスよりファイバー引張強度においてきわめて優れる
ことが記載されているが、前記500 kg/mm2の
強度には遠く及ばない。SiO □ 65% by weight as a substitute for the E glass
(hereinafter simply referred to as %), AIZO:l 25%, MgO
The composition disclosed in British Patent No. 1209244 (commonly known as S glass) represented by 10% or 5i
Oz 60χ, AIZO325%, MgO6%, CaO
There is a composition disclosed in French Patent No. 1435073, which is represented by 9% (commonly known as R glass), and
Although it has been described that fiber tensile strength is extremely superior to glass, it is far from reaching the strength of 500 kg/mm2.
本発明の目的は1650℃以下の工業的温度で溶融でき
、容易に成型、すなわちファイバリングできるとともに
、従来公知のものよりさらに優れ、450 kg/mm
”以上もの引張強度を有するファイバーガラス組成物を
提供することにある。The object of the present invention is to melt at an industrial temperature of 1,650°C or less, to easily mold, i.e., form fibers, and to be superior to conventionally known products, with a weight of 450 kg/mm.
``The purpose of this invention is to provide a fiberglass composition having a tensile strength of the above.''
本発明は重量%で、Si0□52〜56、AIZ032
8〜32、CaOおよびMgO9〜12であり、Y2O
3、La2O3またはCeO,の1種以上が4〜7より
なるファイバーガラス組成物からなる。In the present invention, in weight%, Si0□52-56, AIZ032
8-32, CaO and MgO9-12, Y2O
3. A fiberglass composition in which one or more of La2O3 and CeO is 4 to 7.
本発明の組成範囲においてSingは52〜56%の範
囲が好適で、A1zO3、CaO、MgOと共融するこ
とにより液相温度が低下し溶融が容易となる。In the composition range of the present invention, Sing is preferably in the range of 52 to 56%, and eutectic melting with A1zO3, CaO, and MgO lowers the liquidus temperature and facilitates melting.
52%未満では成型性すなわちファイバリングが不充分
となり、また液相温度も上昇する。56%を超えるとフ
ァイバーの引張強度を低下し、あるいは液相温度が上昇
する。If it is less than 52%, moldability, that is, fiber ringing will be insufficient, and the liquidus temperature will also rise. When it exceeds 56%, the tensile strength of the fiber decreases or the liquidus temperature increases.
Ah03は28〜32%の範囲が好適で、液相温度を下
げ、溶融を容易とする。28%未満ではファイバーの引
張強度が低下し、32%を超えると、ファイバリングが
不充分となる。A preferable content of Ah03 is in the range of 28 to 32%, which lowers the liquidus temperature and facilitates melting. If it is less than 28%, the tensile strength of the fiber will decrease, and if it exceeds 32%, fiber ring will be insufficient.
CaOおよびMgOは合計9〜12%をほぼ均衡して用
いることにより、液相温度を低下し、またファイバリン
グを容易とする。CaOおよびMgOが9%未満である
と液相温度を上昇し溶融性を悪化させる。他方12%を
超えるとファイバーの引張強度を低下させる等物性面で
劣る。By using a total of 9 to 12% of CaO and MgO in a substantially balanced manner, the liquidus temperature is lowered and fibering is facilitated. When CaO and MgO are less than 9%, the liquidus temperature increases and the meltability deteriorates. On the other hand, if it exceeds 12%, the tensile strength of the fiber decreases, resulting in poor physical properties.
希土類すなわちY2O3、LazO3またはCentは
、これら1種以上を4%以上導入することにより、液相
温度を大巾に上昇させることなくファイバーの引張強度
を向上させるもので、4%未満では強度の向上に著効を
示さない。他方7%を超えると液相温度が上昇し溶融が
困難となるので7%以下とする。By introducing 4% or more of one or more of these rare earth elements, Y2O3, LazO3, or Cent, the tensile strength of the fiber can be improved without significantly increasing the liquidus temperature. No significant effect was shown. On the other hand, if it exceeds 7%, the liquidus temperature will rise and melting will become difficult, so the content should be 7% or less.
なお、これらのうちではY2O3が比較的ファイバーと
して引張強度を高める効果が大きい。Note that among these, Y2O3 has a relatively large effect of increasing tensile strength as a fiber.
さらに、これらの希土類の導入は化学的耐久性の向上に
効果を奏する。Furthermore, the introduction of these rare earth elements is effective in improving chemical durability.
本発明を実施するにあたり、前記各成分原料は市販の入
手容易な原料を用いればよく、例えば5i(h;珪砂、
AhO3+水酸化アルミニウム、Cab;炭酸カルシウ
ム、)1gO;炭酸マグネシウム、YZO3+酸化イツ
トリウム、LazO:+ ;酸化ランタン、CeO,;
酸化セリウム等が用いられる。In carrying out the present invention, commercially available and easily available raw materials may be used as the raw materials for each component, such as 5i (h; silica sand,
AhO3 + aluminum hydroxide, Cab; calcium carbonate, ) 1gO; magnesium carbonate, YZO3 + yttrium oxide, LazO: +; lanthanum oxide, CeO,;
Cerium oxide or the like is used.
0.5〜0.6%以下の不純成分、例えばNa zo、
K2O、Pez03、Mn0zの混入は差支えない。Z
rO2分は1.5%以下であれば化学的耐久性、引張強
度を向上させるが、それを越えると溶融、ファイバリン
グを悪化する。Impurity components of 0.5 to 0.6% or less, such as Nazo,
There is no problem in mixing K2O, Pez03, and Mn0z. Z
If the rO2 content is 1.5% or less, chemical durability and tensile strength will be improved, but if it exceeds this, melting and fibering will deteriorate.
また溶融清澄剤として1%以下のCaFz、AS20.
.5b203、CaSO4等を混入してもよい。In addition, 1% or less of CaFz, AS20.
.. 5b203, CaSO4, etc. may be mixed.
これら原料を所望組成にもとすき秤量、混合後、タンク
炉、ルツボ炉等任意の溶融手段により1650℃以下、
4時間以下程度で溶融、均質化でき、さらに紡糸炉に導
き1500℃未満で容易にファイバリングすることがで
きる。After preparing these raw materials to the desired composition, weighing them, and mixing them, use any melting means such as a tank furnace or a crucible furnace to melt them at 1650°C or lower.
It can be melted and homogenized in about 4 hours or less, and furthermore, it can be introduced into a spinning furnace and easily fiberized at less than 1500°C.
以下実施例に基づき本発明を説明する。The present invention will be explained below based on Examples.
第1表に示す実施例1〜5および比較例1〜5の組成に
基づき原料調製後、白金ルツボに充填し、電気炉内で1
550℃〜1700℃、2時間〜4時間の適宜温度−時
間で溶融した。その後溶融ガラスを取出し、冷却後小片
を採取し通常の手段で温度勾配炉により液相温度を測定
した。After preparing the raw materials based on the compositions of Examples 1 to 5 and Comparative Examples 1 to 5 shown in Table 1, the raw materials were filled into a platinum crucible and heated in an electric furnace for 1
Melting was carried out at an appropriate temperature and time of 550° C. to 1700° C. for 2 hours to 4 hours. Thereafter, the molten glass was taken out, and after cooling, a small piece was collected and the liquidus temperature was measured using a temperature gradient furnace using a conventional method.
次いでガラスを白金ロジウム裂紡糸炉に投入し1350
〜1500℃の適宜温度で紡糸ノズル約1.7mmφよ
りガラスを引出し、約9μmφのファイバーを得た。各
ファイバーサンプルについては強度試験機で引張強度を
測定した。Next, the glass was put into a platinum-rhodium fission spinning furnace and
The glass was drawn out from a spinning nozzle with a diameter of about 1.7 mm at an appropriate temperature of ~1500°C to obtain a fiber with a diameter of about 9 μm. The tensile strength of each fiber sample was measured using a strength testing machine.
溶融温度−時間、液相温度、紡糸温度、引張強度試験結
果について第1表に併せて示す。The melting temperature-time, liquidus temperature, spinning temperature, and tensile strength test results are also shown in Table 1.
第1表から明らかなように本発明に係る実施例1〜5は
1650℃以下で溶融でき、紡糸性も良好でファイバー
引張強度も450kg/mm”以上と優れている。As is clear from Table 1, Examples 1 to 5 according to the present invention can be melted at 1650° C. or lower, have good spinnability, and have excellent fiber tensile strengths of 450 kg/mm” or higher.
他方比較例1は液相温度が高く粘稠性に富むため溶融温
度が高く、また紡糸温度も高い。またファイバー引張強
度も450 kg/mm2に達しない。On the other hand, Comparative Example 1 has a high liquidus temperature and high viscosity, so the melting temperature is high and the spinning temperature is also high. Furthermore, the fiber tensile strength does not reach 450 kg/mm2.
比較例2.3も同様に引張強度において充分ではない。Comparative Example 2.3 is also not sufficient in tensile strength.
比較例4は希土類導入量が過剰で、1700℃において
も熔融せず実用性に欠ける。比較例5は希土類導入量が
過少でファイバー引張強度の向上に明白な効果を示さな
い等いずれも実施例に比し劣ることが明らかである。In Comparative Example 4, the amount of rare earth introduced was excessive, and it did not melt even at 1700°C, so it lacked practicality. It is clear that Comparative Example 5 is inferior to the Examples in all respects, as the amount of rare earth introduced is too small and does not show any obvious effect on improving the fiber tensile strength.
本発明によれば1650°C以下で溶融できるとともに
ファイバーとして引張強度において優れ、タンミングベ
ルト等常に引張力を受ける複合材として用いても耐久性
に優れるという効果を奏する。According to the present invention, it can be melted at 1650° C. or lower, has excellent tensile strength as a fiber, and has excellent durability even when used as a composite material that is constantly subject to tensile force, such as a tamming belt.
Claims (1)
28〜32、CaOおよびMgO9〜12であり、Y_
2O_3、La_2O_3またはCeO_2の1種以上
が4〜7よりなることを特徴とするファイバーガラス組
成物。1) In weight%, SiO_252-56, Al_2O_3
28-32, CaO and MgO9-12, Y_
A fiberglass composition characterized in that one or more of 2O_3, La_2O_3, or CeO_2 consists of 4 to 7.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13698489A JPH035343A (en) | 1989-05-30 | 1989-05-30 | Fiberglass composition |
GB9011781A GB2233643A (en) | 1989-05-30 | 1990-05-25 | Glass fiber high in tensile strength |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13698489A JPH035343A (en) | 1989-05-30 | 1989-05-30 | Fiberglass composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH035343A true JPH035343A (en) | 1991-01-11 |
Family
ID=15188058
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13698489A Pending JPH035343A (en) | 1989-05-30 | 1989-05-30 | Fiberglass composition |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPH035343A (en) |
GB (1) | GB2233643A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009221104A (en) * | 2003-02-10 | 2009-10-01 | Nippon Electric Glass Co Ltd | Molten glass supply device and method of producing glass formed product |
JP2009221105A (en) * | 2003-02-10 | 2009-10-01 | Nippon Electric Glass Co Ltd | Molten glass supply device and method of producing glass formed product |
WO2013132858A1 (en) * | 2012-03-08 | 2013-09-12 | ニチアス株式会社 | La/Ce-CONTAINING INORGANIC FIBRES THAT ARE SOLUBLE IN PHYSIOLOGICAL SALINE, AND COMPOSITION THEREOF |
JP2018517653A (en) * | 2016-02-29 | 2018-07-05 | ジュシ グループ カンパニー リミテッド | High modulus glass fiber composition and glass fiber and composite material thereof |
CN114085039A (en) * | 2022-01-18 | 2022-02-25 | 山东墨匠新材料科技有限公司 | High-strength high-modulus glass fiber composition, and production method and application of glass fiber |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0895774A3 (en) * | 1997-08-06 | 2002-01-30 | JENERIC/PENTRON Incorporated | Radiopaque dental composites |
JP6081914B2 (en) | 2010-10-18 | 2017-02-15 | オーシーヴィー インテレクチュアル キャピタル リミテッド ライアビリティ カンパニー | High refractive index glass composition |
US9278883B2 (en) | 2013-07-15 | 2016-03-08 | Ppg Industries Ohio, Inc. | Glass compositions, fiberizable glass compositions, and glass fibers made therefrom |
US10035727B2 (en) | 2013-07-15 | 2018-07-31 | Ppg Industries Ohio, Inc. | Glass compositions, fiberizable glass compositions, and glass fibers made therefrom |
US9944551B2 (en) * | 2015-05-07 | 2018-04-17 | Ppg Industries Ohio, Inc. | Glass compositions, fiberizable glass compositions, and glass fibers made therefrom |
CN105753329B (en) | 2016-03-15 | 2018-07-31 | 巨石集团有限公司 | A kind of high-performance glass fiber composition and its glass fibre and composite material |
CN114538784A (en) * | 2020-07-10 | 2022-05-27 | 巨石集团有限公司 | High-modulus glass fiber composition and glass fiber and composite material thereof |
CN113754295B (en) * | 2021-07-31 | 2023-05-09 | 广东金发科技有限公司 | Low-dielectric modified glass fiber and preparation method and application thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5864243A (en) * | 1981-10-13 | 1983-04-16 | Asahi Glass Co Ltd | Glass composition with high elasticity and heat resistance |
JPS62100457A (en) * | 1985-10-28 | 1987-05-09 | Toshiba Monofuratsukusu Kk | Aluminous fiber and its production |
JPS6465045A (en) * | 1987-05-28 | 1989-03-10 | Shimadzu Corp | Oxynitride glass fiber |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1147718A (en) * | 1966-08-31 | 1969-04-02 | Aerojet General Co | High strength glass fibres |
GB1209244A (en) * | 1967-04-05 | 1970-10-21 | Owens Corning Fiberglass Corp | Glass composition |
US3573078A (en) * | 1967-11-16 | 1971-03-30 | United Aircraft Corp | Glass compositions with a high modulus of elasticity |
US3804646A (en) * | 1969-06-11 | 1974-04-16 | Corning Glass Works | Very high elastic moduli glasses |
US3947281A (en) * | 1969-11-06 | 1976-03-30 | United Technologies Corporation | High modulus rare earth and beryllium containing silicate glass compositions |
-
1989
- 1989-05-30 JP JP13698489A patent/JPH035343A/en active Pending
-
1990
- 1990-05-25 GB GB9011781A patent/GB2233643A/en not_active Withdrawn
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5864243A (en) * | 1981-10-13 | 1983-04-16 | Asahi Glass Co Ltd | Glass composition with high elasticity and heat resistance |
JPS62100457A (en) * | 1985-10-28 | 1987-05-09 | Toshiba Monofuratsukusu Kk | Aluminous fiber and its production |
JPS6465045A (en) * | 1987-05-28 | 1989-03-10 | Shimadzu Corp | Oxynitride glass fiber |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009221104A (en) * | 2003-02-10 | 2009-10-01 | Nippon Electric Glass Co Ltd | Molten glass supply device and method of producing glass formed product |
JP2009221105A (en) * | 2003-02-10 | 2009-10-01 | Nippon Electric Glass Co Ltd | Molten glass supply device and method of producing glass formed product |
WO2013132858A1 (en) * | 2012-03-08 | 2013-09-12 | ニチアス株式会社 | La/Ce-CONTAINING INORGANIC FIBRES THAT ARE SOLUBLE IN PHYSIOLOGICAL SALINE, AND COMPOSITION THEREOF |
JPWO2013132858A1 (en) * | 2012-03-08 | 2015-07-30 | ニチアス株式会社 | La / Ce-containing inorganic fiber soluble in physiological saline and composition thereof |
JP2018517653A (en) * | 2016-02-29 | 2018-07-05 | ジュシ グループ カンパニー リミテッド | High modulus glass fiber composition and glass fiber and composite material thereof |
US10239781B2 (en) | 2016-02-29 | 2019-03-26 | Jushi Group Co., Ltd. | High modulus glass fibre composition, and glass fibre and composite material thereof |
US10696581B2 (en) | 2016-02-29 | 2020-06-30 | Jushi Group Co., Ltd. | High-modulus glass fiber composition, glass fiber and composite material therefrom |
CN114085039A (en) * | 2022-01-18 | 2022-02-25 | 山东墨匠新材料科技有限公司 | High-strength high-modulus glass fiber composition, and production method and application of glass fiber |
Also Published As
Publication number | Publication date |
---|---|
GB2233643A (en) | 1991-01-16 |
GB9011781D0 (en) | 1990-07-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3947281A (en) | High modulus rare earth and beryllium containing silicate glass compositions | |
US4363878A (en) | Alkali- and heat-resistant inorganic fiber | |
JP4945711B2 (en) | Glass yarns suitable for reinforcing organic and / or inorganic materials, composites containing these yarns, and compositions used for these yarns | |
JPH035343A (en) | Fiberglass composition | |
JPH06219780A (en) | Glass fiber of low dielectric constant | |
US5330940A (en) | Fiberizable zinc-phosphate glass compositions | |
CA1244485A (en) | Method for utilizing slag from metal production | |
US4818290A (en) | Method for utilizing slag from ferroalloy production | |
JP3132234B2 (en) | Glass long fiber | |
JPS6299B2 (en) | ||
WO1999001393A1 (en) | Glass composition for fibers | |
JPS58502054A (en) | Resistant to alkali glass fiber | |
SU1273339A1 (en) | Glass for glass fibre | |
WO2024105894A1 (en) | Glass fiber and composition for glass fiber | |
JPH08231240A (en) | Composition for high strength glass fiber | |
JP3771073B2 (en) | Glass fiber | |
JPS58167444A (en) | Alkali-resistant glass fiber | |
JPS5860639A (en) | Silicate glass containing rare earth oxide | |
JPH11157876A (en) | Corrosion resistant glass fiber | |
JPH06157072A (en) | Corrosion resistant glass fiber | |
JPS63176340A (en) | Glass fiber and production thereof | |
JPS623785B2 (en) | ||
JP7235915B1 (en) | Glass fibers and compositions for glass fibers | |
WO1989004813A1 (en) | Method for mixing ferrochromium slag in order to produce fire-resistant and chemically resistant fiber | |
JPH0665617B2 (en) | How to use slag from metal production |