JP2000247684A - Glass fiber - Google Patents

Glass fiber

Info

Publication number
JP2000247684A
JP2000247684A JP11056089A JP5608999A JP2000247684A JP 2000247684 A JP2000247684 A JP 2000247684A JP 11056089 A JP11056089 A JP 11056089A JP 5608999 A JP5608999 A JP 5608999A JP 2000247684 A JP2000247684 A JP 2000247684A
Authority
JP
Japan
Prior art keywords
temperature
glass
glass fiber
zro
sio
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
Application number
JP11056089A
Other languages
Japanese (ja)
Other versions
JP3771073B2 (en
Inventor
Mutsumi Unno
睦 海野
Akihiro Koyama
昭浩 小山
Yasukimi Nagashima
廉仁 長嶋
Isamu Kuroda
勇 黒田
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.)
Nippon Sheet Glass Co Ltd
Original Assignee
Nippon Sheet Glass Co Ltd
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 Nippon Sheet Glass Co Ltd filed Critical Nippon Sheet Glass Co Ltd
Priority to JP05608999A priority Critical patent/JP3771073B2/en
Publication of JP2000247684A publication Critical patent/JP2000247684A/en
Application granted granted Critical
Publication of JP3771073B2 publication Critical patent/JP3771073B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C13/00Fibre or filament compositions

Abstract

PROBLEM TO BE SOLVED: To provide a glass fiber which is free from volatile components such as ZnO, B2O3 and F2, does not cause environmental pollution and which is excellent in chemical durability and high in productivity. SOLUTION: The glass fiber contains, by mole, 56 to 63% SiO2, 4 to 9% Al2O3, 0.1 to 3% ZrO2, however, the amount of SiO2+ZrO2-Al2O3 being not less than 52%, 1 to 7% MgO, 21 to 28% CaO, 0 to 1.5% Na2O, and 0 to 1.5% K2O, however, the amount of Na2O+K2O being not more than 1.5%, and is substantially free from ZnO, B2O3 and F2.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】この発明は、実質的にZnO、B
2O3、F2といった揮発成分を含まず、化学的な耐久性に
優れたガラス繊維、特にFRP、プリント配線基盤用樹
脂等の複合材料の補強材として好適なガラス繊維に関す
る。
[0001] The present invention relates to a method for producing ZnO, B
The present invention relates to a glass fiber which does not contain volatile components such as 2 O 3 and F 2 and has excellent chemical durability, particularly a glass fiber suitable as a reinforcing material for a composite material such as FRP and resin for a printed wiring board.

【0002】[0002]

【従来の技術】ガラス繊維を生産するためには、所定の
割合に調合されたガラス原料を高温下で熔融し、均質な
ガラスとした後、多数のノズルを底部にもったブッシン
グにその熔融物を供給し、そのノズル先端よりガラスを
連続的に引き出す方法が用いられている。
2. Description of the Related Art In order to produce glass fibers, a glass material prepared in a predetermined ratio is melted at a high temperature to obtain a homogeneous glass, and then the molten material is formed into a bushing having a number of nozzles at the bottom. Is supplied and glass is continuously drawn from the tip of the nozzle.

【0003】繊維化する場合、ガラスの失透温度が、ガ
ラスを繊維化する際の温度である紡糸温度を越えると失
透物が生成し、ブッシングのノズル付近で糸切れが起こ
りやすくなるので生産性を悪化させる。このためガラス
の失透温度は紡糸温度よりも低いことが繊維化の条件に
なる。
In the case of fiberization, if the devitrification temperature of the glass exceeds the spinning temperature, which is the temperature at which the glass is fiberized, a devitrified material is formed, and the yarn breaks easily near the bushing nozzle. Worsens sex. For this reason, the devitrification temperature of glass is lower than the spinning temperature, which is a condition for fiberization.

【0004】また生産性を向上させるために、紡糸温度
と失透温度との差(△T)をより大きくすることが求め
られるが、ガラスの紡糸温度をあげることは、ブッシン
グの温度調節を難しくするとともに、ブッシングの寿命
が短くなるので好ましくない。さらに原料を高温で熔解
しなければならないので、それに要するエネルギー消費
量も増加する。したがって、紡糸温度は少しでも低い方
が望まれる。
In order to improve the productivity, it is required to increase the difference (ΔT) between the spinning temperature and the devitrification temperature. However, increasing the spinning temperature of glass makes it difficult to control the temperature of the bushing. In addition, the life of the bushing is shortened, which is not preferable. In addition, the raw materials must be melted at high temperatures, which increases the energy consumption required. Therefore, it is desirable that the spinning temperature be as low as possible.

【0005】産業上最も使用されているEガラス繊維
は、その組成物中に紡糸温度や失透温度を下げる役割を
する成分としてB2O3、F2が用いられている。しかしなが
ら、B2O3は原料が高価であること、またB2O3、F2は熔融
行程で揮発しやすいので、周囲の環境汚染を招くことが
問題として示唆されるようになり、B2O3、F2を含まない
新しいガラス繊維が求められている。
[0005] In the E glass fiber which is most used in industry, B 2 O 3 and F 2 are used in the composition as components which lower the spinning temperature and the devitrification temperature. However, B 2 O 3 is that the raw material is expensive, since the B 2 O 3, F 2 is easy to volatilize melting process, now can cause the surrounding environment pollution are suggested as problems, B 2 There is a need for new glass fibers that do not contain O 3 and F 2 .

【0006】このようなB2O3、F2を含有しないガラス繊
維としては、米国特許第3,847,627号、同3,
876,481号、同4,026,715号および同
5,789,329号の各公報に開示されている。
US Pat. Nos. 3,847,627 and 3,847,627 disclose glass fibers containing neither B 2 O 3 nor F 2 .
Nos. 876,481, 4,026,715 and 5,789,329.

【0007】ここで米国特許第3,847,627号お
よび同4,026,715号公報に記載されているガラ
ス繊維の組成は、B2O3、F2を含まないが、それに変わる
融剤として二酸化チタン(TiO2)およびROとして酸化スト
ロンチウム(SrO)、BaO、ZnOが使用されている。また米
国特許第3,876,481号公報に記載されているガ
ラス繊維は、B2O3、F2に代わる融剤として一酸化リチウ
ム(Li2O)、TiO2を含有している。
The composition of glass fibers described in US Pat. Nos. 3,847,627 and 4,026,715 does not contain B 2 O 3 or F 2 , but a flux instead of B 2 O 3 or F 2. Used are titanium dioxide (TiO 2 ), and RO is strontium oxide (SrO), BaO, ZnO. The glass fiber described in U.S. Pat. No. 3,876,481 contains lithium monoxide (Li 2 O) and TiO 2 as fluxes instead of B 2 O 3 and F 2 .

【0008】しかしながら、上記TiO2、Li2O、ZnOは積
極的に導入するには原料が高価である。また、ZnOは熔
融時に揮発し、窯の寿命を低下させる問題がある。さら
に、TiO2はガラスを着色させるので、補強材として使用
した場合外観が損なわれる場合がある。
However, the raw materials of TiO 2 , Li 2 O, and ZnO are expensive to positively introduce them. In addition, ZnO volatilizes during melting and has a problem of shortening the life of the kiln. Further, TiO 2 colors the glass, so that when used as a reinforcing material, the appearance may be impaired.

【0009】米国特許第5,789,329号公報に記
載されているガラス組成は、ZnO、B 2O3、F2といった揮
発成分を含まず、また耐酸性、耐水性といった化学的耐
久性にも優れているが、実施例記載の紡糸温度に相当す
る1,000ポイズ[P]の温度はどれも1,248℃
以上の高温にあるため、生産性とブッシング寿命の低下
が懸念される。
As described in US Pat. No. 5,789,329.
The glass composition listed is ZnO, B TwoOThree, FTwoSuch as
No chemical components such as acid and water resistance
Excellent in durability, but equivalent to the spinning temperature described in the examples.
Temperature of 1,000 poise [P]
High temperature causes reduction of productivity and bushing life
Is concerned.

【0010】[0010]

【発明が解決しようとする課題】本発明は上記の背景を
踏まえたものであり、揮発成分であるZnO、B2O3、F2
含まないことで環境汚染を防止し、化学的耐久性に優
れ、高い生産性を有するガラス繊維を提供することを目
的とする。
SUMMARY OF THE INVENTION The present invention has been made in view of the above background, and does not contain ZnO, B 2 O 3 , and F 2 which are volatile components, thereby preventing environmental pollution and improving chemical durability. It is an object of the present invention to provide a glass fiber having excellent productivity and high productivity.

【0011】[0011]

【課題を解決するための手段】上記目的を達成するため
に、請求項1に記載の発明のガラス繊維は、モルパーセ
ント(以下、単に「%」と表記する)で、SiO2:56〜
63%、Al2O3:4〜9%、ZrO2:0.1〜3%、ただ
しSiO2+ZrO2-Al2O3≧52%、MgO:1〜7%、CaO:2
1〜28%、Na2O:0〜1.5%、K2O:0〜1.5
%、ただしNa2O+K2O≦1.5%を含有し、ZnO、B2O3、F
2を実質的に含まないものである。
Means for Solving the Problems To achieve the above object, the glass fiber according to the first aspect of the present invention has a molar percentage (hereinafter simply referred to as “%”) of SiO 2 : 56 to 50%.
63%, Al 2 O 3 : 4 to 9%, ZrO 2 : 0.1 to 3%, provided that SiO 2 + ZrO 2 -Al 2 O 3 ≧ 52%, MgO: 1 to 7%, CaO: 2
1~28%, Na 2 O: 0~1.5 %, K 2 O: 0~1.5
%, But containing Na 2 O + K 2 O ≦ 1.5%, ZnO, B 2 O 3 , F
2 is not substantially contained.

【0012】請求項2に記載の発明のガラス繊維は、請
求項1の発明の構成に加えて、紡糸温度が1,245℃
以下で、かつ紡糸温度と失透温度の差が40℃以上ある
ものである。
The glass fiber according to the second aspect of the present invention has a spinning temperature of 1,245 ° C. in addition to the constitution of the first aspect of the present invention.
And the difference between the spinning temperature and the devitrification temperature is 40 ° C. or more.

【0013】請求項3に記載の発明のガラス繊維は、モ
ルパーセントで、SiO2:58〜61%、Al2O3:6〜7
%、ZrO2:0.1〜2%、ただしSiO2+ZrO2-Al2O3≧5
3%、MgO:3〜6%、CaO:23〜27%、Na2O:0〜
1%、K2O:0〜1%、ただしNa2O+K2O≦1%を含有
し、ZnO、B2O3、F2を実質的に含まず、紡糸温度が1,
235℃以下で、かつ紡糸温度と失透温度との差が50
℃以上あるものである。
The glass fiber according to the third aspect of the present invention has a molar percentage of SiO 2 : 58-61% and Al 2 O 3 : 6-7.
%, ZrO 2 : 0.1 to 2 %, provided that SiO 2 + ZrO 2 -Al 2 O 3 ≧ 5
3%, MgO: 3~6%, CaO: 23~27%, Na 2 O: 0~
1%, K 2 O: 0 to 1%, but containing Na 2 O + K 2 O ≦ 1%, containing substantially no ZnO, B 2 O 3 and F 2 , and having a spinning temperature of 1,
235 ° C. or less, and the difference between the spinning temperature and the devitrification temperature is 50
It is at least ℃.

【0014】[0014]

【発明の実施の形態】次に、この発明のガラス繊維の構
成成分を上記のように限定した理由を説明する。SiO
2は、ガラスの耐酸性を向上させる成分であり、56%
未満では上記作用が得られず、一方63%より多い場合
はガラスの高温での粘性が上がるため、紡糸温度が上昇
し、またバッチの熔解性が悪化する。このため含有量は
56〜63%であり、58〜61%が望ましい。
Next, the reasons why the constituents of the glass fiber of the present invention are limited as described above will be described. SiO
2 is a component that improves the acid resistance of glass, and is 56%
If it is less than 63%, the above effect cannot be obtained. On the other hand, if it is more than 63%, the viscosity of the glass at a high temperature increases, so that the spinning temperature increases and the meltability of the batch deteriorates. Therefore, the content is 56 to 63%, and preferably 58 to 61%.

【0015】Al2O3は、ガラスの耐水性を改善し、また
適量含有させることで失透性を改善させる成分である。
4%未満の場合は、十分な作用が得られず、9%より多
い場合は耐酸性、熔解性が悪化する。このため含有量
は、4〜9%であり、6〜7%が望ましい。
Al 2 O 3 is a component that improves the water resistance of glass and improves the devitrification property when contained in an appropriate amount.
If it is less than 4%, sufficient action cannot be obtained, and if it is more than 9%, acid resistance and meltability deteriorate. Therefore, the content is 4 to 9%, preferably 6 to 7%.

【0016】ZrO2は、ガラスの化学的な耐久性を向上さ
せ、ガラスの屈折率を増加させ、少量で紡糸温度、失透
温度を低下させるのに特に効果を与える成分である。
0.1%未満では、上記作用が得られず、一方3%より
多い場合はガラスが失透しやすくなったり、熔解性が悪
化する。そのため含有量は、0.1〜3%であり、好ま
しくは0.1〜2%である。
ZrO 2 is a component that improves the chemical durability of the glass, increases the refractive index of the glass, and has a particularly effective effect in lowering the spinning temperature and the devitrification temperature in a small amount.
If it is less than 0.1%, the above effect cannot be obtained, while if it is more than 3%, the glass tends to be devitrified or the meltability deteriorates. Therefore, the content is 0.1 to 3%, preferably 0.1 to 2%.

【0017】ここでSiO2、ZrO2、Al2O3は、ガラスの特
性、特に酸に対する耐久性に影響を与える成分である。
SiO2とZrO2は、耐酸性を向上させる成分であり、Al2O3
は耐酸性を悪化させる成分であり、特にSiO2+ZrO2-Al2O
3の値が52%以上の場合に耐酸性が良好であることを
見い出した。このため、SiO2+ZrO2-Al2O3≧52%であ
り、好ましくはSiO2+ZrO2-Al2O3≧53%以上である。
Here, SiO 2 , ZrO 2 , and Al 2 O 3 are components that affect the properties of the glass, particularly the durability against acids.
SiO 2 and ZrO 2 are components for improving acid resistance, and Al 2 O 3
Is a component that deteriorates the acid resistance, particularly SiO 2 + ZrO 2 -Al 2 O
It was found that when the value of 3 was 52% or more, the acid resistance was good. Therefore, SiO 2 + ZrO 2 —Al 2 O 3 ≧ 52%, preferably SiO 2 + ZrO 2 —Al 2 O 3 ≧ 53%.

【0018】MgOは、高温粘性を下げる作用を発揮し、
かつ紡糸性とバッチ熔解性を向上させる成分であり、1
%未満では上記作用が得られない。一方、7%より多い
場合はガラスが失透しやすくなり、生産性が低下する。
このため含有量は、1〜7%であり、3〜6%が好まし
く、5〜6%が望ましい。
MgO exhibits the effect of lowering the viscosity at high temperatures,
And a component that improves spinnability and batch meltability;
%, The above effect cannot be obtained. On the other hand, if it is more than 7%, the glass tends to be devitrified, and the productivity is reduced.
Therefore, the content is 1 to 7%, preferably 3 to 6%, and more preferably 5 to 6%.

【0019】CaOは、ガラスの耐水性や失透性を向上さ
せるとともに、ガラスの粘度を低下させ、熔解性と紡糸
性を向上させる成分である。21%未満の場合、上記作
用が得られない。28%より多くなる場合はガラスが失
透しやすくなるため、その含有量は21〜28%であ
り、23〜27%が望ましい。
CaO is a component that improves the water resistance and devitrification of the glass, reduces the viscosity of the glass, and improves the meltability and spinnability. If it is less than 21%, the above effect cannot be obtained. If the content is more than 28%, the glass tends to be devitrified. Therefore, the content is 21 to 28%, and preferably 23 to 27%.

【0020】Na2O、K2Oといったアルカリ金属酸化物
は、ガラスの融剤であり、熔解性を向上させると共に、
少量でも失透温度を低下させる効果を発揮する。しか
し、これらのアルカリ金属酸化物の合計量が1.5%を
超えると、化学的耐久性が悪化するので好ましくない。
このため含有量は、Na2O:0〜1.5%、K2O:0〜
1.5%、かつNa2O+K2O≦1.5%であり、好ましくは
Na2O:0〜1%、K2O:0〜1%、かつNa2O+K2O≦1%
である。
Alkali metal oxides such as Na 2 O and K 2 O are fluxing agents for glass and improve the melting property.
Even a small amount exhibits the effect of lowering the devitrification temperature. However, when the total amount of these alkali metal oxides exceeds 1.5%, the chemical durability deteriorates, which is not preferable.
Therefore content, Na 2 O: 0~1.5%, K 2 O: 0~
1.5%, and Na 2 O + K 2 O ≦ 1.5%, preferably
Na 2 O: 0 to 1%, K 2 O: 0 to 1%, and Na 2 O + K 2 O ≦ 1%
It is.

【0021】この発明においては、上記成分以外に、Sr
O、酸化マンガン(MnO)、酸化鉄II(FeO)、酸化鉄III(Fe2
O3)、TiO2、B2O3、F2などが原料の不純物として、合計
で0.5%以下の範囲で混入することがある。
In the present invention, in addition to the above components, Sr
O, manganese oxide (MnO), iron oxide II (FeO), iron oxide III (Fe 2
O 3), TiO 2, B 2 O 3, F 2 , etc. as impurities in the raw material, may be mixed in a range of 0.5% or less in total.

【0022】またガラス清澄剤として三酸化硫黄(S
O3)、酸化アンチモン(Sb2O3)を少量含むことがある。し
かしながら清澄剤を除く他の成分は、ガラスを着色した
り、また直接導入するには原料が高価であることから、
安価なガラス繊維を提案することに対して好ましくな
い。さらにZnO、B2O3、F2は製造工程において揮発し、
環境を汚染するので好ましくない。なお、この発明にお
いて、ZnO、B2O3、F2を実質的に含まないとは、不純物
として含むことはあっても、意図的に含有させることは
ないという趣旨である。
As a glass fining agent, sulfur trioxide (S
O 3 ) and a small amount of antimony oxide (Sb 2 O 3 ). However, other components except the fining agent color the glass, and since the raw material is expensive to introduce directly,
It is not preferable to propose an inexpensive glass fiber. Furthermore, ZnO, B 2 O 3 and F 2 volatilize in the manufacturing process,
It is not preferable because it pollutes the environment. In the present invention, “substantially not containing ZnO, B 2 O 3 , and F 2” means that although it is contained as an impurity, it is not intentionally contained.

【0023】[0023]

【実施例】以下、本発明のガラス繊維を実施例に基づい
て詳細に説明する。
The glass fiber of the present invention will be described below in detail with reference to examples.

【0024】[0024]

【表1】 [Table 1]

【0025】[0025]

【表2】 [Table 2]

【0026】「表1」および「表2」に示した組成を有
するガラスを調製し、紡糸温度、失透温度、耐水性およ
び耐酸性を測定した。まず、「表1」および「表2」に
示すガラス組成となるように、粘土、珪砂、石灰石、苦
灰石、アルミナおよび酸化ジルコニウムを調合し、白金
坩堝を用いて1,500℃で6時間熔融した。熔融後、
融液を金属プレート上に流し出し厚さ約5mmの板状に成
形、徐冷し、特性測定用のガラスを得た。紡糸温度、す
なわち1,000Pに相当する温度は、通常の白金球引
き上げ法により測定した。
Glasses having the compositions shown in Tables 1 and 2 were prepared, and the spinning temperature, devitrification temperature, water resistance and acid resistance were measured. First, clay, silica sand, limestone, dolomite, alumina and zirconium oxide are mixed so as to have the glass composition shown in Table 1 and Table 2, and the mixture is heated at 1,500 ° C. for 6 hours using a platinum crucible. Melted. After melting,
The melt was poured out onto a metal plate, formed into a plate having a thickness of about 5 mm, and gradually cooled to obtain a glass for property measurement. The spinning temperature, that is, the temperature corresponding to 1,000 P, was measured by a usual platinum ball pulling-up method.

【0027】また失透温度は、以下のように測定した。
すなわち板状のガラスの一部を粉砕し、直径1,190
〜1,680μmの粒状にしてからアルコールで洗浄し
た後、白金ボートに入れ、長さ方向に温度勾配のついた
電気炉内に2時間保持した。電気炉から上記ボートを取
り出して放冷した後、50倍の偏光顕微鏡を用いて結晶
の出現位置を直接観察し、その最高温度を失透温度とし
た。
The devitrification temperature was measured as follows.
That is, a part of the plate-like glass is pulverized to have a diameter of 1,190.
After being granulated to 1,1,680 μm and washed with alcohol, it was placed in a platinum boat and kept in an electric furnace having a temperature gradient in the length direction for 2 hours. After the boat was taken out of the electric furnace and allowed to cool, the appearance position of the crystal was directly observed using a polarizing microscope of 50 times magnification, and the highest temperature was defined as the devitrification temperature.

【0028】耐酸性は、板状のガラスを粉砕し、直径4
20〜590μmの粒状にしてからアルコールで洗浄
し、比重グラム精秤し、80℃の10%H2SO4溶液中に
浸漬し、72時間経過したところで重量減少率[%]を
算出した。また耐酸性はこの重量減少率が小さいほど良
いことを示す。
The acid resistance is as follows.
After granulation of 20 to 590 μm, the particles were washed with alcohol, weighed precisely with a specific gravity of gram, immersed in a 10% H 2 SO 4 solution at 80 ° C., and after 72 hours, the weight loss rate [%] was calculated. The acid resistance shows that the smaller the weight reduction rate is, the better.

【0029】耐水性は、JIS R3502に基づく方
法でアルカリ溶出量を測定することで調べた。この量が
少ないほど、耐水性の良いことを表している。
The water resistance was examined by measuring the amount of alkali elution by a method based on JIS R3502. The smaller the amount, the better the water resistance.

【0030】実施例1〜9の各試料は、いずれも耐酸性
による重量減少率が0.7%以下、耐水性は0.006
mg以下、屈折率は1.565以上と良好な値を示した。
また、紡糸温度を表す1,000Pに相当する温度も
1,245℃以下であり、ブッシングの温度制御性が容
易に行える。さらに、紡糸温度と失透温度との差△Tが
40℃以上であるため、紡糸時に失透が生成しにくく、
高い生産性を維持することができる。
Each of the samples of Examples 1 to 9 had a weight loss rate of 0.7% or less due to acid resistance and a water resistance of 0.006 or less.
mg or less, and the refractive index was a good value of 1.565 or more.
Further, the temperature corresponding to 1,000 P representing the spinning temperature is also 1,245 ° C. or less, so that the bushing temperature controllability can be easily performed. Furthermore, since the difference ΔT between the spinning temperature and the devitrification temperature is 40 ° C. or more, devitrification hardly occurs during spinning,
High productivity can be maintained.

【0031】比較例1は市販のEガラスであり、耐酸性
が悪く、環境を汚染するB2O3、F2が含まれている。また
比較例2は米国特許第3,847,627号公報記載の
実施例(No.24)で、ZrO2が入っているものの、Zn
O、TiO2を含み、かつ紡糸温度は低いが、失透温度が高
いので、生産性を示唆する△Tが小さくなり、安定した
生産は難しい。比較例3は、米国特許第5,789,3
29号公報記載の紡糸温度が最も低い実施例(No.
5)であるが、紡糸温度は1,248℃と高く、ブッシ
ングの温度制御性や寿命に問題がある。
Comparative Example 1 is a commercially available E glass, which has poor acid resistance and contains B 2 O 3 and F 2 which pollute the environment. Comparative Example 2 is an example (No. 24) described in U.S. Pat. No. 3,847,627, in which ZrO 2 is contained but Zn is contained.
Although O and TiO 2 are contained and the spinning temperature is low, the devitrification temperature is high, so that ΔT, which indicates productivity, becomes small, and stable production is difficult. Comparative Example 3 is described in US Pat. No. 5,789,3.
Example having the lowest spinning temperature described in Japanese Patent Publication No. 29 (No. 29).
However, the spinning temperature is as high as 1,248 ° C., and there is a problem in the temperature controllability and life of the bushing.

【0032】以上のようにこの発明のガラス繊維は、優
れた生産性、紡糸性を有し、化学的耐久性に優れ、FR
Pやプリント配線基盤等の補強材料として有用である。
As described above, the glass fiber of the present invention has excellent productivity, spinnability, excellent chemical durability, and FR
It is useful as a reinforcing material for P and printed wiring boards.

【0033】[0033]

【発明の効果】請求項1では、実質的にZnO、B2O3、F2
といった揮発成分を含まず、SiO2、Al2O3、ZrO2、MgO、
CaO、Na2O、K2Oの含有量を限定すると共に、SiO2+ZrO2-
Al2O3およびアルカリ金属酸化物の合計量を限定するこ
とで、化学的な耐久性に優れたガラス繊維が得られる。
According to the first aspect, ZnO, B 2 O 3 , F 2
It does not contain volatile components such as SiO 2 , Al 2 O 3 , ZrO 2 , MgO,
While limiting the content of CaO, Na 2 O, K 2 O, SiO 2 + ZrO 2-
By limiting the total amount of Al 2 O 3 and alkali metal oxide, glass fiber excellent in chemical durability can be obtained.

【0034】請求項2では、請求項1に記載される範囲
内でも特に紡糸温度と△T(紡糸温度−失透温度)を限
定することで、より紡糸性、生産性に優れたガラス繊維
が得られる。
According to the second aspect, the glass fiber having more excellent spinnability and productivity can be obtained by limiting the spinning temperature and ΔT (spinning temperature−devitrification temperature) even in the range described in the first aspect. can get.

【0035】請求項3では、特にSiO2、Al2O3、MgOの組
成範囲を限定することで、紡糸温度と△Tに優れ、さら
に耐酸性、耐水性も良好なガラス繊維が得られる。
According to the third aspect, particularly, by limiting the composition range of SiO 2 , Al 2 O 3 , and MgO, a glass fiber excellent in spinning temperature and ΔT, and further excellent in acid resistance and water resistance can be obtained.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 長嶋 廉仁 大阪府大阪市中央区道修町3丁目5番11号 日本板硝子株式会社内 (72)発明者 黒田 勇 大阪府大阪市中央区道修町3丁目5番11号 日本板硝子株式会社内 Fターム(参考) 4G062 AA05 BB01 CC10 DA06 DB03 DC01 DD01 DE01 DF01 EA01 EB01 EB02 EB03 EC01 EC02 EC03 ED03 EE04 EF01 EG01 FA01 FB01 FC02 FC03 FD01 FE01 FF01 FG01 FH01 FJ01 FK01 FL01 GA01 GA10 GB01 GC01 GD01 GE01 HH01 HH03 HH05 HH07 HH09 HH11 HH13 HH15 HH17 HH20 JJ01 JJ03 JJ05 JJ07 JJ10 KK01 KK03 KK05 KK07 KK10 MM15 MM28 NN33 NN34  ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Nasuhito Nagashima 3-5-1, Doshomachi, Chuo-ku, Osaka-shi, Japan Inside Nippon Sheet Glass Co., Ltd. (72) Inventor Isamu Kuroda 3 Doshucho, Chuo-ku, Osaka-shi, Osaka 5-11, Nippon Sheet Glass Co., Ltd. F-term (reference) 4G062 AA05 BB01 CC10 DA06 DB03 DC01 DD01 DE01 DF01 EA01 EB01 EB02 EB03 EC01 EC02 EC03 ED03 EE04 EF01 EG01 FA01 FB01 FC02 FC03 FD01 FE01 F01 GA01 F01 GB01 GC01 GD01 GE01 HH01 HH03 HH05 HH07 HH09 HH11 HH13 HH15 HH17 HH20 JJ01 JJ03 JJ05 JJ07 JJ10 KK01 KK03 KK05 KK07 KK10 MM15 MM28 NN33 NN34

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 モルパーセントで、 二酸化ケイ素(SiO2):56〜63%、 酸化アルミニウム(Al2O3):4〜9%、 酸化ジルコニウム(ZrO2):0.1〜3%、 ただし、SiO2+ZrO2-Al2O3≧52%、 酸化マグネシウム(MgO):1〜7%、 酸化カルシウム(CaO):21〜28%、 一酸化ナトリウム(Na2O):0〜1.5%、 酸化カリウム(K2O):0〜1.5%、 ただし、Na2O+K2O≦1.5% を含有し、酸化亜鉛(ZnO)、三酸化二ホウ素(B2O3)、フ
ッ素(F2)を実質的に含まないガラス繊維。
1. In mole percent, silicon dioxide (SiO 2 ): 56-63%, aluminum oxide (Al 2 O 3 ): 4-9%, zirconium oxide (ZrO 2 ): 0.1-3%, , SiO 2 + ZrO 2 -Al 2 O 3 ≧ 52%, magnesium oxide (MgO): 1 to 7%, calcium oxide (CaO): 21 to 28%, sodium monoxide (Na 2 O): 0 to 1. 5%, potassium oxide (K 2 O): 0 to 1.5%, provided that it contains Na 2 O + K 2 O ≦ 1.5%, zinc oxide (ZnO), diboron trioxide (B 2 O 3 ) Glass fiber substantially free of fluorine (F 2 ).
【請求項2】 紡糸温度が1,245℃以下で、かつ紡
糸温度と失透温度の差が40℃以上ある請求項1記載の
ガラス繊維。
2. The glass fiber according to claim 1, wherein the spinning temperature is 1,245 ° C. or lower, and the difference between the spinning temperature and the devitrification temperature is 40 ° C. or higher.
【請求項3】 モルパーセントで、SiO2:58〜61
%、Al2O3:6〜7%、ZrO2:0.1〜2%、ただしSiO
2+ZrO2-Al2O3≧53%、MgO:3〜6%、CaO:23〜2
7%、Na2O:0〜1%、K2O:0〜1%、ただしNa2O+K2
O≦1%を含有し、ZnO、B2O3、F2を実質的に含まず、紡
糸温度が1,235℃以下で、紡糸温度と失透温度との
差が50℃以上あるガラス繊維。
3. SiO 2 : 58-61 in mole percent.
%, Al 2 O 3: 6~7 %, ZrO 2: 0.1~2%, provided that SiO
2 + ZrO 2 -Al 2 O 3 ≧ 53%, MgO: 3 to 6%, CaO: 23 to 2
7%, Na 2 O: 0 to 1%, K 2 O: 0 to 1%, provided that Na 2 O + K 2
Glass fiber containing O ≦ 1%, containing substantially no ZnO, B 2 O 3 , and F 2 , having a spinning temperature of 1,235 ° C. or less, and a difference between the spinning temperature and the devitrification temperature of 50 ° C. or more .
JP05608999A 1999-03-03 1999-03-03 Glass fiber Expired - Fee Related JP3771073B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP05608999A JP3771073B2 (en) 1999-03-03 1999-03-03 Glass fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP05608999A JP3771073B2 (en) 1999-03-03 1999-03-03 Glass fiber

Publications (2)

Publication Number Publication Date
JP2000247684A true JP2000247684A (en) 2000-09-12
JP3771073B2 JP3771073B2 (en) 2006-04-26

Family

ID=13017382

Family Applications (1)

Application Number Title Priority Date Filing Date
JP05608999A Expired - Fee Related JP3771073B2 (en) 1999-03-03 1999-03-03 Glass fiber

Country Status (1)

Country Link
JP (1) JP3771073B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005511469A (en) * 2001-12-07 2005-04-28 デー ベー ヴェー フィーバー ノイハウス ゲーエムベーハー Continuous glass fiber with improved heat resistance
WO2007004608A1 (en) 2005-07-05 2007-01-11 Nippon Electric Glass Co., Ltd. Glass fiber composition, glass fiber and glass fiber-containing composite material
US7285508B2 (en) 2003-08-29 2007-10-23 Nippon Sheet Glass Company, Limited Glass flake
JP2013047184A (en) * 2005-07-05 2013-03-07 Nippon Electric Glass Co Ltd Glass fiber composition, glass fiber, and glass fiber-containing composite material
WO2023190980A1 (en) * 2022-03-30 2023-10-05 日本板硝子株式会社 Glass fiber

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005511469A (en) * 2001-12-07 2005-04-28 デー ベー ヴェー フィーバー ノイハウス ゲーエムベーハー Continuous glass fiber with improved heat resistance
JP4821017B2 (en) * 2001-12-07 2011-11-24 デーベーヴェー ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング Continuous glass fiber with improved heat resistance
US7285508B2 (en) 2003-08-29 2007-10-23 Nippon Sheet Glass Company, Limited Glass flake
WO2007004608A1 (en) 2005-07-05 2007-01-11 Nippon Electric Glass Co., Ltd. Glass fiber composition, glass fiber and glass fiber-containing composite material
JP2007039320A (en) * 2005-07-05 2007-02-15 Nippon Electric Glass Co Ltd Glass fiber composition, glass fiber and glass fiber-containing composite material
US7989375B2 (en) 2005-07-05 2011-08-02 Nippon Electric Glass Co., Ltd. Glass fiber composition, glass fiber, and glass fiber containing composition material
JP2013047184A (en) * 2005-07-05 2013-03-07 Nippon Electric Glass Co Ltd Glass fiber composition, glass fiber, and glass fiber-containing composite material
WO2023190980A1 (en) * 2022-03-30 2023-10-05 日本板硝子株式会社 Glass fiber

Also Published As

Publication number Publication date
JP3771073B2 (en) 2006-04-26

Similar Documents

Publication Publication Date Title
US4199364A (en) Glass composition
AU764638B2 (en) Glass with high proportion of zirconium-oxide and its uses
US6818575B2 (en) Glass fiber forming compositions
TWI405734B (en) Method of manufacturing high performance glass fibers in a refractory lined melter and fiber formed thereby
US5789329A (en) Boron-free glass fibers
US8173560B2 (en) Glass yarns capable of reinforcing organic and/or inorganic materials
CA2769401C (en) Improved modulus, lithium free glass
TW201031613A (en) Composition for high performance glass fibers and fibers formed therewith
CA2360850A1 (en) Glass with high proportion of zirconium-oxide and its uses
JP2001080933A (en) Crystal glass not containing lead and barium
GB2237017A (en) Alkali-resistant glass for forming glass fibres.
JP7466729B2 (en) Electronic grade glass fiber composition, glass fiber and electronic grade glass fiber fabric
CA2745050A1 (en) Glass fiber composition
JP2000247683A (en) Corrosion resistant glass fiber
EP1189846A1 (en) Glass fiber composition
WO2018123327A1 (en) Glass composition for glass fiber, glass fiber, and method for producing glass fiber
JP3771073B2 (en) Glass fiber
EP1546051B1 (en) Low-temperature, fluoride free fiber glass compositions and products made using same
JP2015006973A (en) Composition for glass fiber, glass fiber and manufacturing method of glass fiber
WO1999001393A1 (en) Glass composition for fibers
JP2509329B2 (en) Glass for optical fiber
JP3248279B2 (en) Composition for antibacterial glass
JPWO2012017694A1 (en) Glass filler
EP0098648B1 (en) Optical fibres having a large numerical aperture
JP2000264675A (en) Glass for optical fiber

Legal Events

Date Code Title Description
A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20040521

RD03 Notification of appointment of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7423

Effective date: 20040715

RD04 Notification of resignation of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7424

Effective date: 20040715

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20050510

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20050708

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20051025

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20051124

A911 Transfer of reconsideration by examiner before appeal (zenchi)

Free format text: JAPANESE INTERMEDIATE CODE: A911

Effective date: 20051206

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20060117

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20060208

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100217

Year of fee payment: 4

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100217

Year of fee payment: 4

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313117

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100217

Year of fee payment: 4

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100217

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110217

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120217

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130217

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130217

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140217

Year of fee payment: 8

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees