JP2022151758A - Glass composition with low thermal expansion coefficient and glass fiber - Google Patents
Glass composition with low thermal expansion coefficient and glass fiber Download PDFInfo
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- 239000000203 mixture Substances 0.000 title claims abstract description 117
- 239000011521 glass Substances 0.000 title claims abstract description 116
- 239000003365 glass fiber Substances 0.000 title claims abstract description 46
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 53
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000005751 Copper oxide Substances 0.000 claims abstract description 34
- 229910000431 copper oxide Inorganic materials 0.000 claims abstract description 34
- 239000000395 magnesium oxide Substances 0.000 claims abstract description 29
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims abstract description 29
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims abstract description 29
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 28
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000011787 zinc oxide Substances 0.000 claims abstract description 25
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 24
- 229910052810 boron oxide Inorganic materials 0.000 claims abstract description 22
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000000292 calcium oxide Substances 0.000 claims abstract description 21
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims abstract description 14
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 30
- 239000002019 doping agent Substances 0.000 claims description 17
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 16
- 238000004519 manufacturing process Methods 0.000 claims description 16
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 15
- FZFYOUJTOSBFPQ-UHFFFAOYSA-M dipotassium;hydroxide Chemical compound [OH-].[K+].[K+] FZFYOUJTOSBFPQ-UHFFFAOYSA-M 0.000 claims description 12
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 11
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052681 coesite Inorganic materials 0.000 claims description 2
- 229910052593 corundum Inorganic materials 0.000 claims description 2
- 229910052906 cristobalite Inorganic materials 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 235000012239 silicon dioxide Nutrition 0.000 claims description 2
- 229910052682 stishovite Inorganic materials 0.000 claims description 2
- 229910052905 tridymite Inorganic materials 0.000 claims description 2
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- 239000010949 copper Substances 0.000 claims 1
- 239000005357 flat glass Substances 0.000 description 37
- 238000000034 method Methods 0.000 description 33
- 238000002844 melting Methods 0.000 description 24
- 230000008018 melting Effects 0.000 description 24
- 238000002156 mixing Methods 0.000 description 22
- 230000000052 comparative effect Effects 0.000 description 12
- 238000009987 spinning Methods 0.000 description 12
- 238000005259 measurement Methods 0.000 description 11
- 239000013078 crystal Substances 0.000 description 6
- 238000001556 precipitation Methods 0.000 description 4
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000010292 electrical insulation Methods 0.000 description 3
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 3
- 229910001950 potassium oxide Inorganic materials 0.000 description 3
- 229910001948 sodium oxide Inorganic materials 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- -1 alkali metal salts Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910004283 SiO 4 Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000000930 thermomechanical effect Effects 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 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
- C03C3/093—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/50—Glass production, e.g. reusing waste heat during processing or shaping
- Y02P40/57—Improving the yield, e-g- reduction of reject rates
Abstract
Description
本発明は、ガラス組成物及びガラス繊維に関し、特に、低膨張係数を持つガラス組成物、及びガラス繊維に関するものである。 The present invention relates to glass compositions and glass fibers, and more particularly to glass compositions and glass fibers having a low coefficient of expansion.
ガラス繊維は、優れた電気絶縁性、低消耗性、及び高安定性などの利点を持つので、回路基板、光ファイバー通信、電子製品の外装ケースなどに広く応用されている。例えば、ガラス繊維をプリント基板に適用する場合は、金属箔シート/配線などの電子部品に貼り付けるための絶縁層又は絶縁部に補強材料として添加しており、熱膨張係数の違いによる絶縁層又は絶縁部と金属箔シート/配線との間の剥離の発生を抑制するために、低熱膨張係数(Coefficient of thermal expansion,CTE)を持つガラス繊維の研究開発が進められている。 Glass fiber has advantages such as excellent electrical insulation, low consumption, and high stability, so it is widely used in circuit boards, optical fiber communications, outer casings of electronic products, and the like. For example, when applying glass fiber to a printed circuit board, it is added as a reinforcing material to the insulating layer or insulating part for attaching to electronic parts such as metal foil sheets / wiring, and the insulating layer or insulating part due to the difference in the coefficient of thermal expansion In order to suppress the occurrence of delamination between the insulating portion and the metal foil sheet/wiring, research and development of glass fibers having a low coefficient of thermal expansion (CTE) are underway.
現在市販されている低熱膨張係数のガラス繊維は、熱膨張係数が約3ppm/℃~4ppm/℃の範囲にあるが、ハイテク産業の発展に伴い、配線パターンの設計も日々複雑化しており、製造過程における熱膨張や収縮などによる残留応力が電子部品に影響を与えてしまうため、業界では、より低い熱膨張係数を有するガラス繊維が求められている。 Low thermal expansion coefficient glass fibers currently on the market have a thermal expansion coefficient in the range of about 3 ppm/°C to 4 ppm/°C. The industry is looking for glass fibers with a lower coefficient of thermal expansion, as residual stresses due to thermal expansion and contraction in the process affect electronic components.
このように、本発明は、低熱膨張係数を持つガラス組成物を提供することを目的としている。 Thus, an object of the present invention is to provide a glass composition having a low coefficient of thermal expansion.
上記目的を達成するために、本発明は、低熱膨張係数を持つガラス組成物であって、酸化ケイ素(SiO2)、酸化アルミニウム(Al2O3)、酸化ホウ素(B2O3)、酸化マグネシウム(MgO)、酸化カルシウム(CaO)、酸化亜鉛(ZnO)及び酸化銅(CuO)を含むことを特徴とする。 In order to achieve the above object, the present invention provides a glass composition having a low coefficient of thermal expansion, comprising silicon oxide (SiO 2 ), aluminum oxide (Al 2 O 3 ), boron oxide (B 2 O 3 ), oxide It is characterized by containing magnesium (MgO), calcium oxide (CaO), zinc oxide (ZnO) and copper oxide (CuO).
尚、前記ガラス組成物の重量パーセント100wt%に対して、該酸化ケイ素の含有量は55wt%~63wt%の範囲にあり、該酸化アルミニウムの含有量は15wt%~22wt%の範囲にあり、該酸化ホウ素の含有量は6wt%~13wt%の範囲にあり、該酸化マグネシウムの含有量は5wt%~14wt%の範囲にあり、該酸化カルシウムの含有量は0.1wt%~4wt%の範囲にあり、該酸化亜鉛の含有量は0wt%~8wt%の範囲にあり、該酸化銅の含有量は0.03wt%~7wt%の範囲にあることを特徴とする。 The content of the silicon oxide is in the range of 55 wt% to 63 wt%, the content of the aluminum oxide is in the range of 15 wt% to 22 wt%, and the weight percentage of the glass composition is 100 wt%. The content of boron oxide is in the range of 6 wt% to 13 wt%, the content of magnesium oxide is in the range of 5 wt% to 14 wt%, and the content of calcium oxide is in the range of 0.1 wt% to 4 wt%. The zinc oxide content is in the range of 0 wt % to 8 wt %, and the copper oxide content is in the range of 0.03 wt % to 7 wt %.
また、本発明の他の目的は、低熱膨張係数を持つガラス繊維を提供することである。 Another object of the present invention is to provide a glass fiber with a low coefficient of thermal expansion.
上記目的を達成するために、本発明は、前述の低熱膨張係数を持つガラス組成物からなるガラス繊維であって、該ガラス繊維の熱膨張係数が3ppm/℃以下であることを特徴とする。 In order to achieve the above objects, the present invention is characterized by a glass fiber made of the glass composition having a low coefficient of thermal expansion, wherein the coefficient of thermal expansion of the glass fiber is 3 ppm/°C or less.
本発明の異質な効果とは、本発明の低熱膨張係数を持つガラス組成物中の酸化銅の含有量を増加させ、酸化亜鉛の含有量を減少させることにより、当該低熱膨張係数を持つガラス組成物からなるガラス繊維の熱膨張係数を3ppm/℃以下に低減させることにある。 The heterogeneous effect of the present invention is that the content of copper oxide in the glass composition having a low coefficient of thermal expansion of the present invention is increased and the content of zinc oxide is decreased, so that the glass composition having a low coefficient of thermal expansion To reduce the coefficient of thermal expansion of a glass fiber made of a material to 3 ppm/° C. or less.
本発明に係る低熱膨張係数を持つガラス組成物は、低熱膨張係数を持つガラス繊維を製造するために用いられる。概略的に説明すると、当該ガラス繊維は、本発明のガラス組成物を十分に混合した後、高温で溶融、紡糸などの工程を順次行うことにより製造され、熱膨張係数は3ppm/℃以下である。 A glass composition with a low coefficient of thermal expansion according to the present invention is used to produce a glass fiber with a low coefficient of thermal expansion. Briefly, the glass fiber is produced by sufficiently mixing the glass composition of the present invention and then performing processes such as melting and spinning at a high temperature in sequence, and has a coefficient of thermal expansion of 3 ppm/° C. or less. .
本発明のガラス組成物の一つの実施例においては、酸化ケイ素(SiO2)、酸化アルミニウム(Al2O3)、酸化ホウ素(B2O3)、酸化マグネシウム(MgO)、酸化カルシウム(CaO)、酸化亜鉛(ZnO)、酸化銅(CuO)、及びドーパントを含む。 In one embodiment of the glass composition of the present invention, silicon oxide ( SiO2 ), aluminum oxide ( Al2O3 ) , boron oxide ( B2O3), magnesium oxide (MgO), calcium oxide (CaO). , zinc oxide (ZnO), copper oxide (CuO), and dopants.
具体的に述べると、前記ガラス組成物の重量パーセント100wt%に対して、該酸化ケイ素の含有量は55wt%~63wt%の範囲にあり、該酸化アルミニウムの含有量は15wt%~22wt%の範囲にあり、該酸化ホウ素の含有量は6wt%~13wt%の範囲にあり、該酸化マグネシウムの含有量は5wt%~14wt%の範囲にあり、該酸化カルシウムの含有量は0.1wt%~4wt%の範囲にあり、該酸化亜鉛の含有量は0wt%~8wt%の範囲にあり、該酸化銅の含有量は0.03wt%~7wt%の範囲にあり、該ドーパントの含有量は1.2wt%以下である。 Specifically, the silicon oxide content ranges from 55 wt% to 63 wt% and the aluminum oxide content ranges from 15 wt% to 22 wt%, based on a weight percentage of 100 wt% of the glass composition. , the content of boron oxide is in the range of 6 wt% to 13 wt%, the content of magnesium oxide is in the range of 5 wt% to 14 wt%, and the content of calcium oxide is in the range of 0.1 wt% to 4 wt% %, the zinc oxide content is in the range of 0 wt % to 8 wt %, the copper oxide content is in the range of 0.03 wt % to 7 wt %, and the dopant content is 1.0 wt % to 8 wt %. 2 wt % or less.
本発明のガラス組成物における、酸化ケイ素、酸化アルミニウム及び酸化ホウ素は、前記ガラス繊維を構成する主成分であり、そのうち酸化ケイ素は、網目形成成分(Network former)であることから、その四面体の結晶格子構造[SiO4]で連続した網目構造を形成して、本発明のガラス組成物からなるガラス繊維の主要な構造となる。酸化アルミニウムは、本発明のガラス組成物の中間体(intermediate)となるものであり、酸化ケイ素における一部の酸素原子と結合して架橋酸素を形成して、該ガラス組成物の熱安定性及び粘度をさらに高めるために用いられるが、該酸化アルミニウムの含有量が多すぎると、当該ガラス組成物の粘度が高くなり、その後のガラス繊維の製造工程において、大量の加熱エネルギーを供給しなければならず、生産コストの増大を招いてしまう。酸化ホウ素は、四面体の結晶格子構造での酸化ケイ素と結合して、安定した連続構造を形成することができ、また、製造工程においての高温状態下では粘度を下げ、結晶析出を抑える作用があり、一方、製造工程においての低温状態下ではガラス構造の緊密度を向上させ、当該ガラス組成物の熱膨張係数を低下させることができるが、該酸化ホウ素の含有量が多すぎると、製造工程の高温状態で過度の蒸発が起こり、当該ガラス組成物の組成に変動が生じ、該ガラス組成物の電気絶縁性にも影響を及ぼしてしまう。 Silicon oxide, aluminum oxide and boron oxide in the glass composition of the present invention are the main components constituting the glass fiber, and among them, silicon oxide is a network former, so that the tetrahedral The crystal lattice structure [SiO 4 ] forms a continuous network structure and becomes the main structure of the glass fiber made of the glass composition of the present invention. Aluminum oxide serves as an intermediate of the glass composition of the present invention, and bonds with some oxygen atoms in silicon oxide to form bridging oxygen, thereby improving the thermal stability and thermal stability of the glass composition. Although it is used to further increase the viscosity, if the aluminum oxide content is too high, the viscosity of the glass composition will be high, and a large amount of heating energy must be supplied in the subsequent glass fiber manufacturing process. Instead, it leads to an increase in production costs. Boron oxide can combine with silicon oxide in the tetrahedral crystal lattice structure to form a stable continuous structure, and also has the effect of reducing viscosity and suppressing crystal precipitation under high temperature conditions in the manufacturing process. On the other hand, it is possible to improve the tightness of the glass structure and reduce the thermal expansion coefficient of the glass composition under low temperature conditions in the manufacturing process. Excessive vaporization occurs at high temperatures of 100 to 100 psi, causing fluctuations in the composition of the glass composition and also affecting the electrical insulation properties of the glass composition.
本実施例においては、前記ガラス組成物の重量パーセント100wt%に対して、前記酸化ケイ素の含有量は55wt%~63wt%の範囲にあり、前記酸化アルミニウムの含有量は15wt%~22wt%の範囲にあり、前記酸化ホウ素の含有量は6wt%~13wt%の範囲にある。尚、該酸化ホウ素の含有量は、6wt%~11wt%の範囲にあることが好ましく、また、該酸化ケイ素と酸化アルミニウムと酸化ホウ素の含有量の合計は、84wt%~90wt%の範囲にあることが好ましい。 In this example, the content of the silicon oxide is in the range of 55 wt% to 63 wt%, and the content of the aluminum oxide is in the range of 15 wt% to 22 wt%, relative to the weight percentage of 100 wt% of the glass composition. and the boron oxide content is in the range of 6 wt % to 13 wt %. The content of the boron oxide is preferably in the range of 6 wt% to 11 wt%, and the total content of the silicon oxide, aluminum oxide and boron oxide is in the range of 84 wt% to 90 wt%. is preferred.
酸化マグネシウム及び酸化カルシウムは、本発明のガラス組成物の高温時の粘度を適度に減少させることができるので、製造時における当該ガラス組成物の溶融を促進させるが、該酸化カルシウムの含有量が多すぎると、結晶析出現象が増えてしまい、この場合、酸化マグネシウムの添加は当該ガラス組成物の機械的強度を高めるのに役立つが、酸化マグネシウムの含有量が多すぎると、ガラス構造の緊密度が落ち、熱膨張係数の低減に不利となる。 Magnesium oxide and calcium oxide can moderately reduce the viscosity of the glass composition of the present invention at high temperatures, and thus promote the melting of the glass composition during production. If the content is too high, the phenomenon of crystal precipitation increases. In this case, the addition of magnesium oxide helps increase the mechanical strength of the glass composition. This is disadvantageous for reducing the coefficient of thermal expansion.
本実施例においては、前記ガラス組成物の重量パーセント100wt%に対して、前記酸化マグネシウムの含有量は5wt%~14wt%の範囲にあり、前記酸化カルシウムの含有量は0.1wt%~4wt%にある。尚、該酸化マグネシウムの含有量は5wt%~9.5wt%、該酸化カルシウムの含有量は0.1wt%~0.4wt%の範囲にあることが好ましい。 In this example, the content of the magnesium oxide is in the range of 5 wt% to 14 wt%, and the content of the calcium oxide is in the range of 0.1 wt% to 4 wt%, relative to the weight percentage of 100 wt% of the glass composition. It is in. The magnesium oxide content is preferably in the range of 5 wt % to 9.5 wt %, and the calcium oxide content is preferably in the range of 0.1 wt % to 0.4 wt %.
酸化亜鉛及び酸化銅の添加は、本発明に係るガラス繊維の熱膨張係数の低減に役立つものであり、本実施例においては、前記ガラス組成物の重量パーセント100wt%に対して、該酸化亜鉛の含有量は0wt%~8wt%の範囲にあり、該酸化銅の含有量は0.03wt%~7wt%の範囲にある。しかしながら、一般的なガラス組成物には、アルカリ金属塩類(例えば、酸化カリウム、酸化ナトリウムなど)も添加されるが、ガラス組成物がアルカリ金属塩類を含むと、酸化亜鉛の存在により、かえって当該ガラス組成物本来の緻密な構造が緩くなり、膨張係数の低減に不利となる。従って、一部の実施例においては、ガラス組成物がアルカリ金属塩類などの成分を含有する場合、必要に応じて酸化亜鉛を添加しなくてもよい。 The addition of zinc oxide and copper oxide helps reduce the coefficient of thermal expansion of the glass fibers of the present invention, and in this example, the zinc oxide content is The content is in the range of 0 wt % to 8 wt %, and the content of the copper oxide is in the range of 0.03 wt % to 7 wt %. However, alkali metal salts (e.g., potassium oxide, sodium oxide, etc.) are also added to common glass compositions. The original dense structure of the composition becomes loose, which is disadvantageous in reducing the coefficient of expansion. Therefore, in some embodiments, zinc oxide may optionally be omitted when the glass composition contains ingredients such as alkali metal salts.
本発明では、ガラス繊維の熱膨張係数をさらに下げるために酸化銅を添加することにより、当該ガラス繊維の熱膨張係数を低減させると共に、ガラス組成物は製造工程において緻密な構造を形成する傾向があり、酸化亜鉛によるガラス組成物の構造の粗雑化を抑制することができる。しかしながら、酸化銅の含有量が7wt%を超えると、生成されたガラス繊維中の結晶析出現象が増加する傾向にあり、その後の使用に不利となる。 In the present invention, by adding copper oxide to further lower the thermal expansion coefficient of the glass fiber, the thermal expansion coefficient of the glass fiber is reduced, and the glass composition tends to form a dense structure during the manufacturing process. It is possible to suppress coarsening of the structure of the glass composition due to zinc oxide. However, when the content of copper oxide exceeds 7 wt %, the phenomenon of crystal precipitation in the produced glass fibers tends to increase, which is disadvantageous for subsequent use.
一部の実施例においは、前記ガラス組成物の重量パーセント100wt%に対して、添加された酸化銅の含有量は0.5wt%~7wt%の範囲にあるが、これに限定されるものではなく、該酸化銅の含有量が4wt%~7wt%の範囲にあり、該酸化銅と酸化亜鉛の含有量の合計が4.5wt%~7wt%の範囲にあることが好ましい。尚、他の実施例においては、該酸化マグネシウムと酸化亜鉛と酸化銅の含有量の合計が12wt%~15wt%の範囲にあってもよい。 In some embodiments, the content of copper oxide added ranges from 0.5 wt% to 7 wt%, based on a weight percentage of 100 wt% of the glass composition, but is not limited thereto. It is preferable that the content of the copper oxide is in the range of 4 wt % to 7 wt %, and the total content of the copper oxide and zinc oxide is in the range of 4.5 wt % to 7 wt %. In another embodiment, the total content of magnesium oxide, zinc oxide and copper oxide may be in the range of 12 wt % to 15 wt %.
本実施例においては、前記ガラス組成物の重量パーセント100wt%に対して、該ドーパントの含有量が1.2wt%以下であり、該ドーパントは、酸化ナトリウム、酸化カリウム、酸化鉄及び二酸化チタンのうちの少なくとも一種を含有しており、該ドーパントがもたらす利点の一部は、ガラス組成物以外の微量成分に由来する。 In this example, the content of the dopant is 1.2 wt% or less with respect to 100 wt% by weight of the glass composition, and the dopant is selected from among sodium oxide, potassium oxide, iron oxide and titanium dioxide. Some of the benefits provided by the dopant derive from minor components other than the glass composition.
前記酸化ナトリウム、酸化カリウムなどのアルカリ性酸化物は、本発明のガラス組成物の耐酸性を向上させると共に、当該ガラス組成物の融点を下げ、ガラス繊維の製造に役立つが、これらアルカリ性酸化物の含有量が多すぎると、生成されたガラス繊維の化学的安定性が低下すると共に、当該ガラス繊維の電気絶縁性及び機械的強度も低下する。前記酸化鉄は、ガラス組成物の製造における溶融、紡糸などの工程においての安定性を向上させることができるが、酸化鉄の含有量が多すぎると、当該ガラス組成物の製造において温度ムラが発生する。前記二酸化チタンは、ガラス組成物の機械的強度を高めるのに役立つが、含有量が多すぎると、当該ガラス組成物の製造において結晶析出現象を起こしやすい。 Alkaline oxides such as sodium oxide and potassium oxide improve the acid resistance of the glass composition of the present invention, lower the melting point of the glass composition, and are useful for the production of glass fibers. If the amount is too high, the chemical stability of the glass fibers produced will be reduced, as well as the electrical insulation and mechanical strength of the glass fibers. The iron oxide can improve the stability in steps such as melting and spinning in the production of the glass composition, but if the iron oxide content is too high, temperature unevenness occurs in the production of the glass composition. do. The titanium dioxide serves to increase the mechanical strength of the glass composition, but if the content is too high, crystal precipitation is likely to occur during the production of the glass composition.
以下、本発明の各実施形態に係るガラス組成物について、第1~第9実施例を用いて説明する。また、後述する第1~第9実施例及び第1、第2比較例のガラス組成物からなるガラス繊維の熱膨張係数を表1にまとめた。 Hereinafter, glass compositions according to respective embodiments of the present invention will be described using first to ninth examples. Table 1 summarizes the thermal expansion coefficients of the glass fibers made from the glass compositions of first to ninth examples and first and second comparative examples, which will be described later.
<熱膨張係数の測定方法>
本発明の実施例においては、熱膨張係数の測定を熱機械分析装置(日立製作所製)により行い°C、その測定方法では、まず、ガラス組成物を溶融して、板状ガラス(寸法約0.5cm*0.5cm*2cm)を得て、その後、該板状ガラスを10°C/minの温度上昇速度で加熱し、50°C~200°Cの温度範囲で当該板状ガラスの伸び量を測定して、平均熱膨張係数を算出する。
<Method for measuring coefficient of thermal expansion>
In the examples of the present invention, the coefficient of thermal expansion was measured with a thermomechanical analyzer (manufactured by Hitachi, Ltd.) °C. .5 cm * 0.5 cm * 2 cm), then the sheet glass is heated at a temperature increase rate of 10 ° C / min, and the elongation of the sheet glass is measured in the temperature range of 50 ° C to 200 ° C Quantities are measured to calculate the average coefficient of thermal expansion.
<第1実施例>
本実施例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約59.4wt%の酸化ケイ素と、約19.1wt%の酸化アルミニウムと、約6.5wt%の酸化ホウ素と、約4.4wt%の酸化亜鉛と、約0.4wt%の酸化カルシウムと、約9.1wt%の酸化マグネシウムと、約0.1wt%の酸化銅と、約1.0wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.03wt%の酸化カリウム(K2O)、0.3wt%の酸化鉄(Fe2O3)及び0.64wt%の二酸化チタン(TiO2))とを含有する。
<First embodiment>
In this example, the weight percent of the glass composition is 100 wt%, and the following components by weight: about 59.4 wt% silicon oxide; 5 wt.% boron oxide, about 4.4 wt.% zinc oxide, about 0.4 wt.% calcium oxide, about 9.1 wt.% magnesium oxide, about 0.1 wt.% copper oxide, about 1.5 wt. 0 wt% of said dopants (0.03 wt% sodium oxide ( Na2O ), 0.03 wt% potassium oxide (K2O) , 0.3 wt% iron oxide ( Fe2O3 ) and 0.64 wt% of titanium dioxide (TiO 2 )).
上述した第1実施例のガラス組成物を十分に混合した後、1500℃~1550℃の温度で溶融し、その後、成形、裁断、研磨などの工程を経て、該第1実施例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第1実施例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、2.90ppm/℃の熱膨張係数を得て、さらに、その後、混合、溶融、紡糸などの工程を経て、低熱膨張係数を持つガラス繊維を得る。 After sufficiently mixing the glass composition of the first example described above, it is melted at a temperature of 1500° C. to 1550° C., and then subjected to steps such as molding, cutting, and polishing to obtain the glass composition of the first example. To obtain a sheet glass consisting of Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of the first example was measured according to the above-described method for measuring the thermal expansion coefficient, and was 2.90 ppm/°C. and then through processes such as mixing, melting, spinning, etc., to obtain glass fibers with a low thermal expansion coefficient.
尚、ガラス組成物に混合、溶融、紡糸などの工程を施すことにより得る、板状ガラスまたはガラス繊維に関する製造条件パラメータ及び具体的な製造工程は、当業者にとって周知技術であり、また、成分によっては、関連する製造条件パラメータが若干異なる場合があるが、これらの製造条件パラメータの調整は、当業者にとって周知の技術であるので、ここでその詳細な説明は省略する。 The manufacturing condition parameters and specific manufacturing processes for sheet glass or glass fiber obtained by subjecting a glass composition to processes such as mixing, melting, and spinning are well known to those skilled in the art, and depending on the components may have slightly different related manufacturing condition parameters, but adjustment of these manufacturing condition parameters is a well-known technique for those skilled in the art, so a detailed description thereof will be omitted here.
<第2実施例>
本実施例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約56.3wt%の酸化ケイ素と、約19.2wt%の酸化アルミニウムと、約10.0wt%の酸化ホウ素と、約6.5wt%の酸化亜鉛と、約0.2wt%の酸化カルシウムと、約6.2wt%の酸化マグネシウムと、約0.5wt%の酸化銅と、約1.1wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.03wt%の酸化カリウム(K2O)、0.34wt%の酸化鉄(Fe2O3)及び0.7wt%の二酸化チタン(TiO2))とを含有する。
<Second embodiment>
In this example, the weight percent of the glass composition is 100 wt%, and the components having the following weight percents are: about 56.3 wt% silicon oxide; 0 wt% boron oxide, about 6.5 wt% zinc oxide, about 0.2 wt% calcium oxide, about 6.2 wt% magnesium oxide, about 0.5 wt% copper oxide, and about 1.5 wt%. 1 wt% of said dopants (0.03 wt% sodium oxide ( Na2O ), 0.03 wt% potassium oxide (K2O) , 0.34 wt% iron oxide ( Fe2O3 ) and 0.7 wt% of titanium dioxide (TiO 2 )).
上述した第2実施例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第2実施例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第2実施例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、2.64ppm/℃の熱膨張係数を得て、さらに、その後、混合、溶融、紡糸などの工程を経て、低熱膨張係数を持つガラス繊維を得る。 A sheet glass made of the glass composition of the second embodiment is obtained by successively subjecting the glass composition of the second embodiment to processes such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of the second example was measured according to the above-described method for measuring the thermal expansion coefficient. and then through processes such as mixing, melting, spinning, etc., to obtain glass fibers with a low thermal expansion coefficient.
<第3実施例>
本実施例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約56.4wt%の酸化ケイ素と、約19.2wt%の酸化アルミニウムと、約11.0wt%の酸化ホウ素と、約6.5wt%の酸化亜鉛と、約0.2wt%の酸化カルシウムと、約5.2wt%の酸化マグネシウムと、約0.5wt%の酸化銅と、約1.0wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.03wt%の酸化カリウム(K2O)、0.3wt%の酸化鉄(Fe2O3)及び0.64wt%の二酸化チタン(TiO2))とを含有する。
<Third embodiment>
In this example, the weight percent of the glass composition is 100 wt%, and the following components by weight: about 56.4 wt% silicon oxide; 0 wt% boron oxide, about 6.5 wt% zinc oxide, about 0.2 wt% calcium oxide, about 5.2 wt% magnesium oxide, about 0.5 wt% copper oxide, and about 1.5 wt%. 0 wt% of said dopants (0.03 wt% sodium oxide ( Na2O ), 0.03 wt% potassium oxide (K2O) , 0.3 wt% iron oxide ( Fe2O3 ) and 0.64 wt% of titanium dioxide (TiO 2 )).
上述した第3実施例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第3実施例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第3実施例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、2.70ppm/℃の熱膨張係数を得て、さらに、その後、混合、溶融、紡糸などの工程を経て、低熱膨張係数を持つガラス繊維を得る。 A sheet glass made of the glass composition of the third example is obtained by successively subjecting the glass composition of the third example to processes such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of the third example was measured according to the above-described method for measuring the thermal expansion coefficient, and was 2.70 ppm/°C. and then through processes such as mixing, melting, spinning, etc., to obtain glass fibers with a low thermal expansion coefficient.
<第4実施例>
本実施例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約59.4wt%の酸化ケイ素と、約19.1wt%の酸化アルミニウムと、約6.5wt%の酸化ホウ素と、約3.5wt%の酸化亜鉛と、約0.4wt%の酸化カルシウムと、約9.1wt%の酸化マグネシウムと、約1.0wt%の酸化銅と、約1.0wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.03wt%の酸化カリウム(K2O)、0.3wt%の酸化鉄(Fe2O3)及び0.64wt%の二酸化チタン(TiO2))とを含有する。
<Fourth embodiment>
In this example, the weight percent of the glass composition is 100 wt%, and the following components by weight: about 59.4 wt% silicon oxide; 5 wt% boron oxide, about 3.5 wt% zinc oxide, about 0.4 wt% calcium oxide, about 9.1 wt% magnesium oxide, about 1.0 wt% copper oxide, and about 1.0 wt%. 0 wt% of said dopants (0.03 wt% sodium oxide ( Na2O ), 0.03 wt% potassium oxide (K2O) , 0.3 wt% iron oxide ( Fe2O3 ) and 0.64 wt% of titanium dioxide (TiO 2 )).
上述した第4実施例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第4実施例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第4実施例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、2.82ppm/℃の熱膨張係数を得て、さらに、その後、混合、溶融、紡糸などの工程を経て、低熱膨張係数を持つガラス繊維を得る。 A sheet glass made of the glass composition of the fourth example is obtained by successively subjecting the glass composition of the fourth example to processes such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of the fourth example was measured according to the above-described method for measuring the thermal expansion coefficient, and was 2.82 ppm/°C. and then through processes such as mixing, melting, spinning, etc., to obtain glass fibers with a low thermal expansion coefficient.
<第5実施例>
本実施例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約59.4wt%の酸化ケイ素と、約19.1wt%の酸化アルミニウムと、約6.5wt%の酸化ホウ素と、約2.5wt%の酸化亜鉛と、約0.4wt%の酸化カルシウムと、約9.1wt%の酸化マグネシウムと、約2.0wt%の酸化銅と、約1.0wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.03wt%の酸化カリウム(K2O)、0.3wt%の酸化鉄(Fe2O3)及び0.64wt%の二酸化チタン(TiO2))とを含有する。
<Fifth embodiment>
In this example, the weight percent of the glass composition is 100 wt%, and the following components by weight: about 59.4 wt% silicon oxide; 5 wt% boron oxide, about 2.5 wt% zinc oxide, about 0.4 wt% calcium oxide, about 9.1 wt% magnesium oxide, about 2.0 wt% copper oxide, and about 1.5 wt%. 0 wt% of said dopants (0.03 wt% sodium oxide ( Na2O ), 0.03 wt% potassium oxide (K2O) , 0.3 wt% iron oxide ( Fe2O3 ) and 0.64 wt% of titanium dioxide (TiO 2 )).
上述した第5実施例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第5実施例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第5実施例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、2.80ppm/℃の熱膨張係数を得て、さらに、その後、混合、溶融、紡糸などの工程を経て、低熱膨張係数を持つガラス繊維を得る。 A sheet glass made of the glass composition of the fifth example is obtained by successively subjecting the glass composition of the fifth example to processes such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of the fifth example was measured according to the above-described method for measuring the thermal expansion coefficient, and it was 2.80 ppm/°C. and then through processes such as mixing, melting, spinning, etc., to obtain glass fibers with a low thermal expansion coefficient.
<第6実施例>
本実施例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約59.4wt%の酸化ケイ素と、約19.1wt%の酸化アルミニウムと、約6.5wt%の酸化ホウ素と、約0.4wt%の酸化カルシウムと、約9.1wt%の酸化マグネシウムと、約4.5wt%の酸化銅と、約1.0wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.03wt%の酸化カリウム(K2O)、0.3wt%の酸化鉄(Fe2O3)及び0.64wt%の二酸化チタン(TiO2))とを含有する。
<Sixth embodiment>
In this example, the weight percent of the glass composition is 100 wt%, and the following components by weight: about 59.4 wt% silicon oxide; 5 wt% boron oxide, about 0.4 wt% calcium oxide, about 9.1 wt% magnesium oxide, about 4.5 wt% copper oxide, and about 1.0 wt% of said dopants (0.03 wt% of sodium oxide ( Na2O ), 0.03 wt% potassium oxide (K2O), 0.3 wt% iron oxide ( Fe2O3 ) and 0.64 wt% titanium dioxide ( TiO2 )) contains.
上述した第6実施例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第6実施例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第6実施例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、2.65ppm/℃の熱膨張係数を得て、さらに、その後、混合、溶融、紡糸などの工程を経て、低熱膨張係数を持つガラス繊維を得る。 A sheet glass made of the glass composition of the sixth example is obtained by successively subjecting the glass composition of the sixth example to processes such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of Example 6 was measured according to the above-described method for measuring the thermal expansion coefficient. and then through processes such as mixing, melting, spinning, etc., to obtain glass fibers with a low thermal expansion coefficient.
<第7実施例>
本実施例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約59.4wt%の酸化ケイ素と、約19.2wt%の酸化アルミニウムと、約6.5wt%の酸化ホウ素と、約0.3wt%の酸化カルシウムと、約7.1wt%の酸化マグネシウムと、約6.5wt%の酸化銅と、約1.0wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.03wt%の酸化カリウム(K2O)、0.3wt%の酸化鉄(Fe2O3)及び0.64wt%の二酸化チタン(TiO2))とを含有する。
<Seventh embodiment>
In this example, the weight percent of the glass composition is 100 wt%, and the following components by weight: about 59.4 wt% silicon oxide; 5 wt% boron oxide, about 0.3 wt% calcium oxide, about 7.1 wt% magnesium oxide, about 6.5 wt% copper oxide, and about 1.0 wt% of said dopants (0.03 wt% of sodium oxide ( Na2O ), 0.03 wt% potassium oxide (K2O), 0.3 wt% iron oxide ( Fe2O3 ) and 0.64 wt% titanium dioxide ( TiO2 )) contains.
上述した第7実施例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第7実施例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第7実施例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、2.39ppm/℃の熱膨張係数を得て、さらに、その後、混合、溶融、紡糸などの工程を経て、低熱膨張係数を持つガラス繊維を得る。 A sheet glass made of the glass composition of the seventh embodiment is obtained by successively subjecting the glass composition of the seventh embodiment to processes such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of Example 7 was measured according to the above-described method for measuring the thermal expansion coefficient. and then through processes such as mixing, melting, spinning, etc., to obtain glass fibers with a low thermal expansion coefficient.
<第8実施例>
本実施例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約59.4wt%の酸化ケイ素と、約20.8wt%の酸化アルミニウムと、約6.5wt%の酸化ホウ素と、約0.2wt%の酸化カルシウムと、約5.5wt%の酸化マグネシウムと、約6.5wt%の酸化銅と、約1.1wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.03wt%の酸化カリウム(K2O)、0.34wt%の酸化鉄(Fe2O3)及び0.7wt%の二酸化チタン(TiO2))とを含有する。
<Eighth embodiment>
In this example, the weight percent of the glass composition is 100 wt%, and the following components by weight: about 59.4 wt% silicon oxide; 5 wt% boron oxide, about 0.2 wt% calcium oxide, about 5.5 wt% magnesium oxide, about 6.5 wt% copper oxide, and about 1.1 wt% of said dopants (0.03 wt% of sodium oxide (Na 2 O), 0.03 wt% potassium oxide (K 2 O), 0.34 wt% iron oxide (Fe 2 O 3 ) and 0.7 wt% titanium dioxide (TiO 2 )). contains.
上述した第8実施例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第8実施例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第8実施例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、2.18ppm/℃の熱膨張係数を得て、さらに、その後、混合、溶融、紡糸などの工程を経て、低熱膨張係数を持つガラス繊維を得る。 A sheet glass made of the glass composition of the eighth embodiment is obtained by successively subjecting the glass composition of the eighth embodiment to processes such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of Example 8 was measured according to the above-described method for measuring the thermal expansion coefficient, and it was 2.18 ppm/°C. and then through processes such as mixing, melting, spinning, etc., to obtain glass fibers with a low thermal expansion coefficient.
<第9実施例>
本実施例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約59.4wt%の酸化ケイ素と、約18.7wt%の酸化アルミニウムと、約6.5wt%の酸化ホウ素と、約0.3wt%の酸化カルシウムと、約7.1wt%の酸化マグネシウムと、約7.0wt%の酸化銅と、約1.0wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.03wt%の酸化カリウム(K2O)、0.3wt%の酸化鉄(Fe2O3)及び0.64wt%の二酸化チタン(TiO2))とを含有する。
<Ninth embodiment>
In this example, the weight percent of the glass composition is 100 wt%, and the following components by weight: about 59.4 wt% silicon oxide; 5 wt% boron oxide, about 0.3 wt% calcium oxide, about 7.1 wt% magnesium oxide, about 7.0 wt% copper oxide, and about 1.0 wt% of said dopant (0.03 wt% of sodium oxide ( Na2O ), 0.03 wt% potassium oxide (K2O), 0.3 wt% iron oxide ( Fe2O3 ) and 0.64 wt% titanium dioxide ( TiO2 )) contains.
上述した第9実施例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第9実施例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第9実施例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、2.33ppm/℃の熱膨張係数を得て、さらに、その後、混合、溶融、紡糸などの工程を経て、低熱膨張係数を持つガラス繊維を得る。 A sheet glass made of the glass composition of the ninth embodiment is obtained by successively subjecting the glass composition of the ninth embodiment to processes such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of the ninth example was measured according to the above-described method for measuring the thermal expansion coefficient. and then through processes such as mixing, melting, spinning, etc., to obtain glass fibers with a low thermal expansion coefficient.
<第1比較例>
本比較例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約60.0wt%の酸化ケイ素と、約20.0wt%の酸化アルミニウムと、約5.0wt%の酸化ホウ素と、約3.0wt%の酸化カルシウムと、約11.0wt%の酸化マグネシウムと、約1.0wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.02wt%の酸化カリウム(K2O)、0.3wt%の酸化鉄(Fe2O3)及び0.65wt%の二酸化チタン(TiO2))とを含有する。
<First Comparative Example>
In this comparative example, the weight percent of the glass composition is 100 wt. 0 wt% boron oxide, about 3.0 wt% calcium oxide, about 11.0 wt% magnesium oxide, about 1.0 wt% of said dopants (0.03 wt% sodium oxide ( Na2O ), 0 .02 wt% potassium oxide (K2O), 0.3 wt% iron oxide ( Fe2O3 ) and 0.65 wt% titanium dioxide ( TiO2 )).
上述した第1比較例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第1比較例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第1比較例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、3.34ppm/℃の熱膨張係数を得た。 A plate glass made of the glass composition of the first comparative example is obtained by successively subjecting the glass composition of the first comparative example to steps such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of the first comparative example was measured according to the above-described method for measuring the thermal expansion coefficient. was obtained.
<第2比較例>
本比較例においては、ガラス組成物の重量パーセントを100wt%として、次の重量パーセントを有する成分、つまり、約60.0wt%の酸化ケイ素と、約20.0wt%の酸化アルミニウムと、約10.0wt%の酸化ホウ素と、約6.0wt%の酸化カルシウムと、約3.0wt%の酸化マグネシウムと、約1.0wt%の前記ドーパント(0.03wt%の酸化ナトリウム(Na2O)、0.02wt%の酸化カリウム(K2O)、0.3wt%の酸化鉄(Fe2O3)及び0.65wt%の二酸化チタン(TiO2))とを含有する。
<Second comparative example>
In this comparative example, the weight percent of the glass composition is 100 wt%, and the components having the following weight percents: about 60.0 wt% silicon oxide, about 20.0 wt% aluminum oxide, and about 10.0 wt%. 0 wt% boron oxide, about 6.0 wt% calcium oxide, about 3.0 wt% magnesium oxide, about 1.0 wt% of said dopant (0.03 wt% sodium oxide ( Na2O ), 0 .02 wt% potassium oxide (K2O), 0.3 wt% iron oxide ( Fe2O3 ) and 0.65 wt% titanium dioxide ( TiO2 )).
上述した第2比較例のガラス組成物に順次混合、溶融などの工程を施すことにより、該第2比較例のガラス組成物からなる板状ガラスを得る。次に、当該板状ガラスを標準測定試料とし、前述の熱膨張係数の測定方法に従って、この第2比較例のガラス組成物からなる板状ガラスの熱膨張係数を測定し、3.11ppm/℃の熱膨張係数を得た。 A plate glass made of the glass composition of the second comparative example is obtained by successively subjecting the glass composition of the second comparative example to steps such as mixing and melting. Next, using the sheet glass as a standard measurement sample, the thermal expansion coefficient of the sheet glass made of the glass composition of the second comparative example was measured according to the above-described method for measuring the thermal expansion coefficient, and was 3.11 ppm/°C. was obtained.
表1からも明らかなように、酸化銅及び酸化亜鉛を添加することにより、本発明の第1~第9実施例のガラス組成物の熱膨張係数は、第1、第2比較例に比べて、3ppm/℃以下に低減することができる。また、ガラス組成物中の酸化銅の含有量が4.5wt%以上であり、且つ、酸化亜鉛を含まない場合(第6~第9実施例)には、当該ガラス繊維の熱膨張係数をさらに2.65ppm/℃以下に低減することができる。さらに、酸化銅の含有量を6.5wt%~7.0wt%(第7~第9実施例)にさらに増加させると、当該ガラス組成物からなる板状ガラスの熱膨張係数が2.4ppm/℃以下に低減される。 As is clear from Table 1, by adding copper oxide and zinc oxide, the thermal expansion coefficients of the glass compositions of the first to ninth examples of the present invention are higher than those of the first and second comparative examples. , can be reduced to 3 ppm/°C or less. Further, when the content of copper oxide in the glass composition is 4.5 wt% or more and zinc oxide is not contained (sixth to ninth examples), the thermal expansion coefficient of the glass fiber is further reduced to It can be reduced to 2.65 ppm/°C or less. Furthermore, when the content of copper oxide was further increased to 6.5 wt% to 7.0 wt% (seventh to ninth examples), the thermal expansion coefficient of the sheet glass made of the glass composition increased to 2.4 ppm/ °C or less.
詳しく説明すると、第1実施例、第4~第6実施例のガラス組成物と比較すると、他の成分の含有量が近い場合、酸化亜鉛の含有量が減少し、酸化銅の含有量が増加することにより、製成されたガラス繊維の熱膨張係数が徐々に低減し、酸化亜鉛の含有量を0wt%に低減し、且つ酸化銅の含有量を4.5wt%(第6実施例)に増加させると、製成されたガラス繊維の熱膨張係数が2.65ppm/℃に低減する。さらに、第6~第9実施例のガラス組成物と比較すると、酸化亜鉛を含まずに、他の成分の含有量がほぼ同じである場合、酸化マグネシウムと酸化カルシウムの含有量を適量に減らして、酸化銅の含有量を7wt%までに増加させることにより、当該ガラス繊維の熱膨張係数を2.4ppm/℃以下(第7~第9実施例)に低減させることができることが分かった。 More specifically, when compared with the glass compositions of Examples 1 and 4 to 6, when the contents of other components are similar, the content of zinc oxide decreases and the content of copper oxide increases. As a result, the thermal expansion coefficient of the produced glass fiber is gradually reduced, the content of zinc oxide is reduced to 0 wt%, and the content of copper oxide is reduced to 4.5 wt% (sixth example). The increase reduces the coefficient of thermal expansion of the glass fibers produced to 2.65 ppm/°C. Furthermore, when compared with the glass compositions of Examples 6 to 9, when zinc oxide is not included and the contents of other components are approximately the same, the contents of magnesium oxide and calcium oxide are appropriately reduced. , it was found that the thermal expansion coefficient of the glass fiber can be reduced to 2.4 ppm/° C. or less (seventh to ninth examples) by increasing the content of copper oxide to 7 wt %.
要約すると、本發明低熱膨張係数を持つガラス組成物は、酸化銅の含有量を増加させ、酸化亜鉛の含有量を減少させ、且つ、酸化マグネシウム及び酸化カルシウムの含有量を適量に減少させることにより、本発明に係るガラス組成物からなるガラス繊維の熱膨張係数を3ppm/℃以下に低減することができることから、本発明に係るガラス繊維を半導体の製造や電子産業に広く適用することが可能となるので、本発明の目的を確実に達成することができる。 In summary, the present glass composition with a low coefficient of thermal expansion can be obtained by increasing the content of copper oxide, decreasing the content of zinc oxide, and appropriately decreasing the content of magnesium oxide and calcium oxide. Since the thermal expansion coefficient of the glass fiber made of the glass composition according to the present invention can be reduced to 3 ppm/°C or less, the glass fiber according to the present invention can be widely applied to semiconductor manufacturing and the electronics industry. Therefore, the object of the present invention can be reliably achieved.
以上の説明は、本発明の好適な実施形態に過ぎず、本発明に対して何ら限定を行うものではない。本発明について、比較的好適な実施形態をもって上記のとおり説明を行ったが、これは本発明を限定するものではなく、すべての当業者が、本発明の技術構想を逸脱しない範囲において、本発明の技術の本質に基づいて上記の実施形態に対して行ういかなる簡単な修正、変更及び修飾も、依然としてすべて本発明の技術構想の範囲に含まれる。
The above description is merely a preferred embodiment of the present invention, and does not limit the present invention in any way. Although the present invention has been described with a relatively preferred embodiment as described above, this is not intended to limit the present invention, and any person skilled in the art can understand the present invention without departing from the technical concept of the present invention. Any simple modifications, changes and modifications made to the above-described embodiments based on the essence of the technology of are all still within the scope of the technical concept of the present invention.
Claims (13)
該ガラス組成物の重量パーセント100wt%に対して、
該酸化ケイ素の含有量は55wt%~63wt%の範囲にあり、
該酸化アルミニウムの含有量は15wt%~22wt%の範囲にあり、
該酸化ホウ素の含有量は6wt%~13wt%の範囲にあり、
該酸化マグネシウムの含有量は5wt%~14wt%の範囲にあり、
該酸化カルシウムの含有量は0.1wt%~4wt%の範囲にあり、
該酸化銅の含有量は0.03wt%~7wt%の範囲にあることを特徴とする低熱膨張係数を持つガラス組成物。 A glass composition having a low coefficient of thermal expansion comprising silicon oxide ( SiO2 ), aluminum oxide ( Al2O3 ) , boron oxide ( B2O3), magnesium oxide (MgO), calcium oxide (CaO) and oxide containing copper (CuO),
For a weight percentage of 100 wt% of the glass composition,
The content of the silicon oxide is in the range of 55 wt% to 63 wt%,
The content of the aluminum oxide is in the range of 15 wt% to 22 wt%,
The boron oxide content is in the range of 6 wt% to 13 wt%,
The magnesium oxide content is in the range of 5 wt% to 14 wt%,
The content of the calcium oxide is in the range of 0.1 wt% to 4 wt%,
A glass composition having a low coefficient of thermal expansion, wherein the copper oxide content is in the range of 0.03 wt % to 7 wt %.
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Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6042247A (en) * | 1983-08-16 | 1985-03-06 | Asahi Glass Co Ltd | Low expansion glass |
JPH07172863A (en) * | 1993-10-27 | 1995-07-11 | Central Glass Co Ltd | Fireproof plate glass |
JP2001220173A (en) * | 2000-01-12 | 2001-08-14 | Carl Zeiss:Fa | Aluminoborosilicate glass containing no alkali metal and its use method |
JP2003238196A (en) * | 2001-12-04 | 2003-08-27 | Okamoto Glass Co Ltd | Heat-resistant glass |
JP2007256764A (en) * | 2006-03-24 | 2007-10-04 | Okamoto Glass Co Ltd | Uv absorbing reflection mirror base plate and reflection mirror using the same |
JP2010053013A (en) * | 2008-07-31 | 2010-03-11 | Ohara Inc | Glass |
JP2016030712A (en) * | 2014-07-29 | 2016-03-07 | キヤノン株式会社 | Glass composition and method for producing the same, and glass member and imaging device |
JP2017001950A (en) * | 2011-09-09 | 2017-01-05 | ピーピージー・インダストリーズ・オハイオ・インコーポレイテッドPPG Industries Ohio,Inc. | Low dielectric glass and fiber glass |
WO2020235284A1 (en) * | 2019-05-17 | 2020-11-26 | 日本電気硝子株式会社 | Glass composition and sealing material |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2012366C3 (en) * | 1970-03-16 | 1980-08-21 | Owens-Illinois, Inc., Toledo, Ohio (V.St.A.) | Glasses of the system SIO2 -Al2 O3 -Cu2 O with low thermal expansion, low density and good thermal shock resistance and their use |
FR2082785A5 (en) * | 1970-03-26 | 1971-12-10 | Owens Illinois Inc | Glass with low thermal expansion |
CN102190445A (en) * | 2010-03-16 | 2011-09-21 | 李胜春 | Low-temperature acid-resistant sintered glass powder |
TWI565675B (en) * | 2011-01-11 | 2017-01-11 | Agy控股公司 | Glass composition with low coefficient of thermal expansion, and glass fiber produced from same |
JP5316728B2 (en) * | 2011-02-01 | 2013-10-16 | 日東紡績株式会社 | Glass fiber |
JP2015006978A (en) * | 2013-05-28 | 2015-01-15 | 日本電気硝子株式会社 | Composite powder, and composite powder paste |
JP6315011B2 (en) * | 2016-03-15 | 2018-04-25 | 旭硝子株式会社 | Alkali-free glass substrate and method for producing alkali-free glass substrate |
JPWO2017217496A1 (en) * | 2016-06-17 | 2019-04-11 | 日本板硝子株式会社 | Laser processing glass |
CN112125529A (en) * | 2020-10-06 | 2020-12-25 | 青岛蓝创科信新能源科技有限公司 | Glass fiber ingredient and glass fiber prepared from same |
-
2021
- 2021-03-25 TW TW110110911A patent/TWI777470B/en active
-
2022
- 2022-01-29 CN CN202210111342.5A patent/CN114230175B/en active Active
- 2022-03-18 JP JP2022043898A patent/JP7387790B2/en active Active
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6042247A (en) * | 1983-08-16 | 1985-03-06 | Asahi Glass Co Ltd | Low expansion glass |
JPH07172863A (en) * | 1993-10-27 | 1995-07-11 | Central Glass Co Ltd | Fireproof plate glass |
JP2001220173A (en) * | 2000-01-12 | 2001-08-14 | Carl Zeiss:Fa | Aluminoborosilicate glass containing no alkali metal and its use method |
JP2003238196A (en) * | 2001-12-04 | 2003-08-27 | Okamoto Glass Co Ltd | Heat-resistant glass |
JP2007256764A (en) * | 2006-03-24 | 2007-10-04 | Okamoto Glass Co Ltd | Uv absorbing reflection mirror base plate and reflection mirror using the same |
JP2010053013A (en) * | 2008-07-31 | 2010-03-11 | Ohara Inc | Glass |
JP2017001950A (en) * | 2011-09-09 | 2017-01-05 | ピーピージー・インダストリーズ・オハイオ・インコーポレイテッドPPG Industries Ohio,Inc. | Low dielectric glass and fiber glass |
JP2016030712A (en) * | 2014-07-29 | 2016-03-07 | キヤノン株式会社 | Glass composition and method for producing the same, and glass member and imaging device |
WO2020235284A1 (en) * | 2019-05-17 | 2020-11-26 | 日本電気硝子株式会社 | Glass composition and sealing material |
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JP7387790B2 (en) | 2023-11-28 |
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