WO2007013538A1 - Inorganic composition - Google Patents
Inorganic composition Download PDFInfo
- Publication number
- WO2007013538A1 WO2007013538A1 PCT/JP2006/314825 JP2006314825W WO2007013538A1 WO 2007013538 A1 WO2007013538 A1 WO 2007013538A1 JP 2006314825 W JP2006314825 W JP 2006314825W WO 2007013538 A1 WO2007013538 A1 WO 2007013538A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- inorganic composition
- composition according
- glass
- component
- inorganic
- 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.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
- C03C3/085—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/831—Preparations for artificial teeth, for filling teeth or for capping teeth comprising non-metallic elements or compounds thereof, e.g. carbon
- A61K6/836—Glass
-
- 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
- C03C10/00—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition
- C03C10/0036—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition containing SiO2, Al2O3 and a divalent metal oxide as main constituents
-
- 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
- C03C10/00—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition
- C03C10/0036—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition containing SiO2, Al2O3 and a divalent metal oxide as main constituents
- C03C10/0045—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition containing SiO2, Al2O3 and a divalent metal oxide as main constituents containing SiO2, Al2O3 and MgO as main constituents
-
- 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
- C03C10/00—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition
- C03C10/0054—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition containing PbO, SnO2, B2O3
-
- 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
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/28—Interference filters
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0306—Inorganic insulating substrates, e.g. ceramic, glass
Definitions
- the present invention relates to an inorganic composition having a large average linear expansion coefficient ⁇ and a small change in expansion curve, and suitable for compounding with metals and organic materials, and particularly relates to glass cells and cusps.
- Phase for example, as a Cristobala filler, it is mixed with glass.
- the glass ceramics exhibiting a high coefficient of thermal expansion for the purpose of squeezing.
- U.S. Pat. No. 3,755 describes the use of nephevin ((a A 1 S io force V light (KA 1 S) LO 4 ) as the main crystal phase.
- nephevin (a A 1 S io force V light (KA 1 S) LO 4 )
- the melting conditions at the time of fabrication of ceramics must be minimal ⁇ and very high at 16 and generally It requires a special melting furnace that can withstand high temperatures such that melting is difficult.
- Japanese Patent Application Laid-Open No. 2000-01-64 describes a high-expansion lath rubber composition with a filler as a filler, but the stowage is 2 to 2700 ° C. In this way, the expansion curve is suitable.
- JP 2 Japanese Patent Application Laid-Open No. 2000-01-64 describes a high-expansion lath rubber composition with a filler as a filler, but the stowage is 2 to 2700 ° C. In this way, the expansion curve is suitable. JP 2
- the coefficient of thermal expansion is close to that of metals and organic materials, and the coefficient of thermal expansion is the same. It is important to increase in proportion to the increase in temperature ⁇ 0, and to reduce soot, lower temperatures are required depending on the melting conditions and crystallization conditions.
- the glass used as the substrate must have good matching with the thermal expansion coefficient of the metal species used as the raw material for the multilayer film inductor.
- ⁇ Amorphous glass has low heat resistance, ⁇ Heating and overcooling, and has a problem of being easily broken o
- the material has a coefficient of linear expansion and good transmittance characteristics. I was able to get
- compositions that is, a preferred embodiment of the present invention is represented by any of the following compositions.
- the molar ratio represented by 2 O 3 / R 2 O is 1 or less, 2 5.
- Inorganic composition characterized by being always 0 or more in the temperature range or structural structure
- ⁇ Taga is o 1
- the structure is 0 lara o 11 a 4 _ x K x A 1 4 S i O! 6 , but 0 ⁇ x ⁇ composition
- the amorphized glass according to constitution 4 characterized in that it contains M + CaO + ZnO + SrO + BaO 0 20% and sunflower.
- the light transmission characteristics at 1 m thickness are 15 5 Onm and 3 ⁇ 45 mm, and the lasing force, misalignment force, or crystallized glass of configurations 1 to 5
- a monore ratio represented by A 1 2 ⁇ 3/2 O is 1 or less
- R is at least one selected from L i, N a and ⁇
- a raw material having a composition in the range of 1 ° C. to 1500 ° C. was melted at a temperature of 120 ° C., and the obtained mother glass was 5 0 0.
- Crystallization at C to 75 ° C. a method for producing a mechanical composition or crystallized glass according to any one of constitutions 1 to 6.
- the component composition is expressed in mass%, it should not be expressed directly.
- the mol% is generally in the following range.
- the monore ratio represented is 0.8 or less, most preferably 0.5 or less.
- the degree of dishing and crystallization in ⁇ n.degree must be increased and meltability is reduced.
- the inorganic composition of the present invention has good matching in terms of expansion coefficient with metal or organic matter.
- the length of the sample at 25 ° C and the length of the sample at T ° C are good matching in terms of expansion coefficient with metal or organic matter.
- the value of da (T) / dT is always greater than or equal to 0 in the temperature TO range of -30 ° C to 70 ° C, more preferably more than 0. Furthermore, in the temperature range of 50 ° C to 300 ° C, da (T) / dT is always greater than or equal to 0 in the temperature TO range of -30 ° C to 70 ° C, more preferably more than 0. Furthermore, in the temperature range of 50 ° C to 300 ° C, da (T) / dT is always greater than or equal to 0 in the temperature TO range of -30 ° C to 70 ° C, more preferably more than 0. Furthermore, in the temperature range of 50 ° C to 300 ° C, da (T) / dT is always greater than or equal to 0 in the temperature TO range of -30 ° C to 70 ° C, more preferably more than 0. Furthermore, in the temperature range of 50 ° C to 300 ° C, da (T) / dT is always greater than or equal to 0 in
- ⁇ ) / d T always has a value of 0 or more, more preferably more than 0-, and the machine composition of the present invention is made of glass, sera, Specialized glass, etc.
- the glass is hatched.
- the crystallized glass is subjected to a heat treatment again on the glass that has been melt-molded, so that a desired crystal can be formed on the glass wall.
- the mechanical composition of the present invention is Na K x A 1 S i O.
- the thermal expansion coefficient that is one of the hundreds of the present invention is
- the machine composition of the present invention has an average linear expansion coefficient of 30 ° C 70 ° C.
- ⁇ 4 is a very important component of the crystal and / or solid solution, especially the power of the lucifer ⁇ .
- As the lower limit of the content 35% is less preferable than glass, and 35% is preferable, 38% is more preferable, and 40% is most preferable.
- a 1 O component is the same as ⁇ si O 2 component.
- the liquid phase if its M is less than 5%, a desired crystal phase can be obtained. 0% is more preferable, 2% is most preferable, and if it exceeds 30%, the moldability is degraded due to an increase in the viscosity of the original glass, so the upper is preferably 30%. 5% better than force, 20% most preferred
- the B 2 O component is an effective component for improving the glass property and can be arbitrarily set.However, the increase in the content causes stabilization of the glass structure. Crystal phase precipitation inside the glass due to heat treatment. Therefore, the desired precipitated crystal phase does not change.
- the upper limit of the amount is 15%, preferably 0%, most preferably 5%.
- the P 2 O 5 component is an optional component that contributes to the nucleation of precipitated crystals, but vitrification occurs when added excessively. So the upper limit of that is
- 0% is more preferable than 5%
- Z r O 2 component on which the machine g of precipitated crystals, precipitation binding SB of but an optional component in excess with improved pronounced effect of chemical durability and mechanical strength improvement rabbi miniaturization and materials If it is added, it becomes difficult to melt the original glass, and ZS i O or the like is likely to be left behind when the glass is melted. Or, ZrO 2 will precipitate after the crystallization process. Therefore, 10% is preferable above the amount. More preferred is 8%, most preferred is 6%.
- the TiO 2 component is an optional component that functions as a nucleating agent for precipitated crystals. In addition, it is a component that has a remarkable effect on improving the chemical properties as well as the formation of precipitated crystals and the improvement of the degree of material. If added, the original glass will be damaged, or T i ⁇
- the upper limit of the amount is preferably 15%, more preferably 10%, and most preferably 6%.
- the Li 2 O component is an effective component in promoting the dissolution S reaction of the raw material and lowering the glass temperature, but increasing the content causes a change in the precipitated crystal phase and deterioration in chemical durability. Wake up. Therefore, the upper limit of the amount is preferably 10%, more preferably 0.8%, and most preferably 5%. This component can be optionally added, but the lower limit is more preferably 1%, and most preferably
- K 2 ⁇ component and ⁇ O component is NK x A 1 4 S i, O
- raw glass Ri I scan this, which is the main crystalline phase and the component contributing also on the viscosity propensity of glass crystal phase and the is One of the components constitute at the same time that put out prayer Te
- the upper limit of content is preferably 25%.
- X 4 is an essential component for precipitating calcite and / or calcite solid solutions as crystals. Under the content for obtaining a crystalline phase, it is preferable to exceed 10%, 2% is more preferable, and 5% is most preferable.
- the Na 2 O component is one of the components constituting the crystal phase that precipitates as the main crystal phase by heat treatment of the original glass, and at the same time contributes to the improvement of the viscosity of the molten glass.
- excessive content is chemical of glass JP2006 / 314825 A component that also contributes to improvement ⁇
- excessive content will deteriorate the chemical durability of glass, so the upper limit of content is preferably 25%, preferably 16% More preferred ⁇ 10% is preferred. Also a
- the upper limit of the a 2 O component is preferably 5% ⁇ , and it is more preferred that it is not contained.
- the MgOCaSORoBaOZnO component is an effective component for improving the viscosity of molten glass and for refining precipitated crystals. However, if excessively added, precipitation H
- the upper limit of the content of each component is less likely to cause adverse effects such as changes in the phase of the rice and reduction in the ability to form glass.
- the upper limit of the total amount of each of these components is preferably 20% ⁇ more preferably 10%, and even more preferably 5% o
- the Sb2O3 component can be added as a glass clearing agent, but the upper limit of content is 1%. ⁇ The upper limit is more preferably 0.5%. More preferred is 0 2%
- one of the methods for producing the inorganic composition according to the present invention is to melt the above-described composition, perform forming and cooling, and then perform heat treatment for To crystal phase precipitation o
- Tables 1 to 5 show examples of inorganic compositions of the present invention (No .:! To 23) and conventional invention B.
- glass forming body After melting at Um. Degree, stirring and homogenizing, glass forming body was obtained through molding and cooling process o After that, it was heat-treated at 500 to 600 ° C for 1 to 10 hours After the formation of crystal nuclei, heat treatment was performed at 55 ° C. to 75 ° C. for 1 to 10 hours to obtain a desired inorganic composition.
- 7 ⁇ ' ⁇ 5 ⁇ ⁇ is an X-ray diffractometer (manufactured by Phillips Co., Ltd., trade name: X'Pert Ichi PD) and an energy analyzer with a single dispersion (manufactured by Hitachi, Ltd., trade name S 1 40) 0 0 N HORIBA, Ltd., quotient ⁇ name EX 4 2 0).
- the linear expansion coefficient was measured using a thermal dilatometer (manufactured by Macintosh, trade name: T D 5 0 0 0 S).
- s Fee is 5 mm in diameter
- the force is applied to a 20 mm cylinder, and the temperature range is from 150 ° C to 320 ° C.
- the temperature rate was set to 4 ° C / min. And calculated from the expansion curve showing the relationship between temperature and elongation.
- the transmittance was measured using a spectrophotometer (manufactured by Nissho i-Isakusho Co., Ltd., trade name: U-400) using a sample polished on both sides to a thickness of 1 mm.
- a spectrophotometer manufactured by Nissho i-Isakusho Co., Ltd., trade name: U-400
- Example 1 Example 2 Example 3 Example 4 Example 5
- the d ⁇ ( ⁇ ) Z dt was confirmed from the temperature-coefficient of thermal expansion curve of the examples, and in all examples, da (T in the temperature range of 50 ° C to 300 ° C. ) It was confirmed that Z dt was 0 or more.
- the inorganic composition of the present invention depends not only on the composition but also on the crystallization temperature. : If the wire plate is capable of expansion and transmittance, the crystallization temperature and / or time can be set long in a wide range of conditions to determine the phase does not change.
- the transmittance value gets worse.
- the tension value is increased.
- the inorganic composition of the present invention is based on its average thermal tension, and it is a metal or organic material.
- the value of the thermal expansion coefficient shows a stable behavior with respect to the warming degree, it is also suitable for other optical materials, for example, temperature compensation or compensation members.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Ceramic Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Glass Compositions (AREA)
- Optical Filters (AREA)
- Dental Preparations (AREA)
- Dental Prosthetics (AREA)
- Magnetic Record Carriers (AREA)
Abstract
Description
明細書 Specification
ハ、、機組成物 Ha, machine composition
技 分野 Technical field
本発明は 、 平均線膨張係数が大き < 、 膨張曲線の変化が少ない、 金属、 有機材料と の複合化に好 な無機組成物に関 し、 と り わけガ ラ スセ ラ 、 ッ ク スに関する。 The present invention relates to an inorganic composition having a large average linear expansion coefficient << and a small change in expansion curve, and suitable for compounding with metals and organic materials, and particularly relates to glass cells and cusps.
背景技 Background technique
高い線膨張係数を示す 成物については、 無機材料と その他 材料と の複合化を 目 的と 前よ り 研究がな されている 金属の 双す激急温つガス一ィ 5 For compounds showing a high linear expansion coefficient, research has been conducted for the purpose of combining inorganic materials with other materials.
接合によ る人ェ ょ Joining people
歯冠 oも 25 Tooth crown o 25
の形 と して 、 リ ューサイ ト をフ ィ ラ一 激ル方号ぴ <||力いにラにるをク 4とら 51 As a form of the site, make the refill site a fiery one. <||
と したセ ラ ヽ Sera し た
へ を o o 2 To the o o 2
-y ク ス 、 、作 例や、 高い線膨張係数を示す結晶 公せ合れ多変ガてなフリ 28 -y kusu,, example and crystal showing high linear expansion coefficient
相 、 例 ばク リ ス トバラ フ イ ラ一 と してガラス と交ぜ高い ルす無成セィチ <一一ガ以そガいまばなこし 25 Phase, for example, as a Cristobala filler, it is mixed with glass.
線膨張特性を示す結晶化 作製した事例があ り 、 また 、 情報 機材平数上て、たののタを4をラるララるさゥさし o 62ト There is an example of crystallization that shows linear expansion characteristics, and the number of information equipment is 4 to 4 times.
部 と しての多 膜フ ィ 基板と しても成膜材と の熱膨張係数Coefficient of thermal expansion with film-forming material even as a multi-layer film substrate
}傾蝕組作バ相用均特れ料作上ぉお以れ号たスのたスムのはをるるるよミら } Incline ensembles, a special grade for the use of sushi
のマ ッ 目 o 31 The eyes o 31
チングのため、 高 線熱膨張係数を示すガラスセラ ミ ッ 許製抑最製事 C報れ号的がたいててた向ををををよラ SととC The glass ceramics exhibiting a high coefficient of thermal expansion for the purpose of squeezing.
ク ス につレ、ての研究等が The research, etc.
公近起第結大細びィ多ていで、てのにめめえきさし i There are a lot of recent events, i
公知技術につレ、てみれ 0 7 3 0 4 号公報ではヽ α In the known technique, Temire 0 7 3 0 4
― 傍層値所れ書ガ晶 o、、たいたスはぁにフもる 3ト -3
ク ォ一ソ 、 ケィ酸 リ とする光フ ィ ルタ用ガラス Quorso, glass for optical filters
。相膜時がォににをくり1 . When the phase film is turned on 1
セラ ミ V ク ス について記載 、 当材料の平均線膨張係数 は 、 1 0 0 °C を に低下す 、 そのた め、 多層膜フ ィ ノレ タ作製時に必要と される 2 の平均線膨張係数と室温時 所焼セ晶いににはクラ oト The average linear expansion coefficient of this material is reduced to 100 ° C. Therefore, the average linear expansion coefficient of 2 required for the production of the multilayer film For room temperature firing,
の平均膨張係数と の数値が と の間で合わず 、 かつ 、 1 成結バ相可望おなラミリ o The average expansion coefficient of and does not match between and, and 1
0 0 °C付近に平均線膨 係 持っために、 高レ、成膜精度 能^す晶ぃスいのをラツミ- を要する多層膜フ タ い欠点があった Due to the average linear expansion in the vicinity of 0 ° C, there was a drawback of a multilayer film that required a high level of film deposition accuracy and a low film thickness.
米国特許第 3 7 5 明 おいては、 ネフェ V ン ( Ν a A 1 S i o 力 V ルライ ト ( K A 1 S ] L O 4 ) を主結晶相 とする ッ ク ついて述べられてお り 、 ま た 、 特開 2 0 0 2 4号公報では、 N a 4 — K A 1U.S. Pat. No. 3,755 describes the use of nephevin ((a A 1 S io force V light (KA 1 S) LO 4 ) as the main crystal phase. In Japanese Patent Laid-Open No. 2 0 0 2 4, N a 4 — KA 1
S i O ( を含有する結晶化ガラスにつレヽて述 ベられてレ、る が 、 セラ ミ ツ ク共に作製時の熔解条件は ヽ 少な < と あ 1 6 高温でなければな らず、 総じて溶融 が困難である と と う な高温に耐える こ と のでさ る特殊 な熔解炉を必要 と 、 結晶化処理において も 7 0 0 °C 一As described for crystallized glass containing S i O (), the melting conditions at the time of fabrication of ceramics must be minimal <and very high at 16 and generally It requires a special melting furnace that can withstand high temperatures such that melting is difficult.
1 2 0 0 。C も の高 め 製造コス ト の上昇が問題と なる 特公昭 6 3 ― 3 1 号公 カーネギアナイ 卜 ネ フェ y ン ( N a o • A Ο )を主結晶相 とする結晶化 ガラスにつレ、て述 てレ 望の結 得るためにナ ト ジ ゥムを多量に含有さ てレ 結果的 化ガラス に含有 されるナ 卜 V クム < 、 た材料 て金属や有機物 と の複合化を行つた に腐 しゃす 性がある。 1 2 0 0. High production cost of C is a problem. Special issue of Shoko 6 3-31 No. 1 Crystallized glass with carnegia nai (N ao • A)) as the main crystal phase In order to achieve the desired results, a large amount of sodium is contained in the resulting glass. It has the ability to scramble.
特開 2 0 0 1 ― 6 4 には、 トバライ ト をフ ィ ラ一 と した高膨 ラス ラスセ ク組成物つレ、て 述ベられているが ス ト は、 2 〜 2 7 0 °Cにお いて膨張曲線が 化す 好適で 。 また、 特開 2 Japanese Patent Application Laid-Open No. 2000-01-64 describes a high-expansion lath rubber composition with a filler as a filler, but the stowage is 2 to 2700 ° C. In this way, the expansion curve is suitable. JP 2
0 0 5 ― 4 1 7 5 報 ク リ ス イ ト を フ ィ ラー と し、 膨張曲線の 変化 ガラ ス ッ ク ス組成物お よぴ 鉛ガラスに 述ベ るが、 材料を作製する ためには 、 母ガラ ィ ラ 合物を るプロセスが必 要と なるため ェ程数の増大 混 α のための材料作製プロ セ ス の増 カロを招 < 。 更に 焼成 して得られたも のは内部空孔 欠陥が存在 し やす < なる o すなわち 光線透過系の材料と しても好 ではなレ、 o 発明の開示 0 0 5 ― 4 1 7 5 Report The change in expansion curve using the crystal as a filler. Glass glass composition and lead glass are described. The process of making the mother glass mixture is necessary. The number of processes will increase. This will lead to an increase in the material production process for mixed α. Furthermore, those obtained by firing are more likely to have internal void defects, that is, they are not preferable as light transmission materials, o Disclosure of the Invention
金属 、 有機材料と のマ Vチングが良好と なる為には 熱膨張係数 が金属や有機材料に近づ < よ 5 同い熱膨張係数を有している こ と また 熱膨張係数が '〉曰度の上昇に対して比例的に増加する こ と が重 要であ <0 、 かつ ス 卜低減のためには、 熔解条件や結晶化処理条 件に いてよ り 低温が求め られる For better matching with metals and organic materials, the coefficient of thermal expansion is close to that of metals and organic materials, and the coefficient of thermal expansion is the same. It is important to increase in proportion to the increase in temperature <0, and to reduce soot, lower temperatures are required depending on the melting conditions and crystallization conditions.
例免ば、 多層膜フ ィ ルタ を作製する際、 基板と なるガラ ス には多 層膜フ ィノレタ の原料と なる金属種と の熱膨張係数につレ、ての良好な マ ッチングが求め られ それに伴レ、熱膨張係数の高レ、ァモノレ フ ァ ス ガラ ス及び結 曰 For example, when manufacturing a multilayer filter, the glass used as the substrate must have good matching with the thermal expansion coefficient of the metal species used as the raw material for the multilayer film inductor. Along with that, high coefficient of thermal expansion, glassy glass and ligation
曰曰化ガラスが求め られてきた o 加えて よ り 精度の高 レ、多 膜フ ィ ルタ を作製する には 室温から成膜 1 [皿曰度 (約 2 5 0 There is a need for glass. O In addition, to produce highly accurate and multi-layer filters, film formation is performed at room temperature.
。C ) に至る まで 多層膜材料である金属膜と 同様に熱膨張係数が狐曰 度に対し比例的に増加する材.料が膜への歪を与えに < < する こ と が 可能と なる ため 必要と されてレ、た . C) A material whose coefficient of thermal expansion increases proportionally to the temperature as in the case of a metal film, which is a multilayer film material, because the material can be used to give strain to the film. Les needed
の点におレ、ては ァモルフ ァ スガラス にて同レ、熱膨張係数を有 するガラス を開発する と は可 だが 、 间い熱膨張係数特性をァモ ノレフ ァ スガラス にて達成させる には ァル力 リ 金属ィ オン及び希土 類ィ ォンの含有が必須でめ り 者は 、 ガラス の化学的耐久性率化 In this regard, it is possible to develop a glass having the same thermal expansion coefficient as that of an amorphous glass, but in order to achieve a short thermal expansion coefficient characteristic with an amorphous glass, It is essential to contain metal ions and rare earth ions.
、 後者は原料価格の上昇及びガラス の着色が問題と なる。 加' X.てIn the latter case, rising raw material prices and glass coloring are problems. Ka 'X.
、 ァモルフ ァ スガラスは耐熱性が低レ、 ヽ 加熱 冷却過 に レ、て 割れやすい問題点がある o ァ Amorphous glass has low heat resistance, ヽ Heating and overcooling, and has a problem of being easily broken o
例えば、 ガラス内部に 一ク ォ一 y等の高膨張特性を示す結 曰 曰曰を ガラス内部に成長させた 晶化ガラス に ¾oいては材料に レヽ線膨張 係数を持たせ かつ良好な透過率特性を得る こ と ができたが、 析出 For example, in the case of crystallized glass with high expansion characteristics such as one-quarter y inside the glass, the material has a coefficient of linear expansion and good transmittance characteristics. I was able to get
«± 曰 «± 曰
m 曰曰 の熱膨張係数が 曰 The coefficient of thermal expansion of m 曰 曰 is 曰
1皿度に つて曲線的に変化するため 、 金属材料 や有機材料のよ う に 広 fo,囲の 曰度域にわたつて熱膨 係数が比例 的に増加する材料と の複合化は容易ではなかつた ο Since it changes in a curved manner with respect to one plate degree, it is not easy to combine with a material such as a metal material or an organic material that has a wide fo, proportionally increased coefficient of thermal expansion over the surrounding temperature range. Ο
また 、 ガラスにフ ィ ラ一を交ぜた後に焼成 し レ、線膨張係数を 持つガラス セラ へ V ク ス材料を作製する場 だと ガラス内部にポ ァ (空孔)が Ρ In addition, when glass is filled with a filler and then baked to produce a glass material with a linear expansion coefficient, pores (holes) are generated inside the glass.
発生して しまレ、 作製した材料の内部 ΡΡ質卑化に繋がる o d .た 、 力 ラス と フ ィ ラ一を交ぜるェ程が增加 し材料物性制御要素 も増加するため 得策ではなレ、 This will lead to the deterioration of the internal quality of the produced material o d, but the increase in the amount of force lath and filler crossing will also increase the material physical property control elements.
本発明者は 上記 題を解決するために鋭思研究した結果、 A 1 As a result of intensive research to solve the above problems, the present inventor has obtained A 1
2 O 3 成分と ァル力 ジ 金属酸化物成分の含有比率を最 化する と によ り 、 熱膨張係数が温度の上昇に対して比例的に增加する無機組 成物が得られる と を見出 し 金属材料や有機材料と の複合化が容It has been found that by optimizing the content ratio of the 2 O 3 component and the di-metal oxide component, an inorganic composition can be obtained in which the thermal expansion coefficient increases proportionally with increasing temperature. Combined with metal and organic materials
^に可能なハ、、機組成物 と り わけ 曰 Possible to ^, machine composition and reason わ け
曰曰化ガラスを提供する に至つた o Leading to providing hatched glass o
すなわち 本発明に好 な態様は以下の 成のいずれかで表され That is, a preferred embodiment of the present invention is represented by any of the following compositions.
^ o^ o
- -
(構成 1 ) A 1 2 o 3 成分と R 2 o成分と で Rは L i(Configuration 1) A 1 2 o 3 component and R 2 o component R is Li
N a Kから選ばれる少な < と も 一種以上を示す を含有し、 A 1Contains a small <selected from N a K and at least one kind of A 1
2 O 3 / R 2 Oで表わされるモル比率が 1 以下であつて 、 2 5 。Cに おける試料の長さ を L 0 T °Cに ける si科の長さ を L と した時 温度 Tにつレ、て d ( T ) / d T = ( 1 / L 0 ) X ( d 2 L / d TThe molar ratio represented by 2 O 3 / R 2 O is 1 or less, 2 5. When the length of the sample in C is L 0 T ° C and the length of the si family is L, the temperature is T, d (T) / d T = (1 / L 0) X (d 2 L / d T
2 ) で表わされる d ( T ) / d Tの値が ― 3 0 。C 7 0 。Cの温 2 ί i ί ί ) で表わされる d a ( T ) / d Τ の値が、 一 3 0 。C〜 7 0 。Cの温 機物記物物お又又のいて Bs S- ί << 2 ) The value of d (T) / dT represented by-is 30. C 7 0. C temperature 2 ί i ί ί) The value of da (T) / d 表 わ is 1 30. C ~ 70. C's warm-up article Bs S- ί <<
度範囲に レ、て常に 0 以上である事を特徴と する無機組成物又は結 構構構構構構範組載構又構又又ていたははよ b aー Inorganic composition characterized by being always 0 or more in the temperature range or structural structure
晶化 ラ ス Crystallization Las
成成成成成成成結結成ガ囲は成ははの oる 9 成 成 成 成 成 9 9 9 9
(構成 2 ) 平均線膨張係数が— 3 0 °C〜 7 0 °Cの温度範囲におい 事結結結物無晶晶の 06007091111 (Constitution 2) In the temperature range of −30 ° C to 70 ° C, the average linear expansion coefficient is amorphous.
て、 6 0 X 1 0 0 X 1 0 —6 0 X 1 0 0 X 1 0 —
%を o 231 一 7 Z °C〜 1 5 7 Z °Cである こ と を特徴 機化化各又 } }}晶晶晶 % O 231 1 7 Z ° C to 1 5 7 Z ° C
とする構成組成特以 BD BD
~たガガは o 1 ~ Taga is o 1
o g に 載の無機組成物又は結晶化ガラス。 o Inorganic composition or crystallized glass listed in g.
(構成 3 ) N (Configuration 3) N
構構徴結上分は 0ララ o 11 a 4 _ x K x A 1 4 S i O ! 6 、 ただ し 0 ≤ x ≤ 成構 The structure is 0 lara o 11 a 4 _ x K x A 1 4 S i O! 6 , but 0 ≤ x ≤ composition
4 、 である結日-曰おょぴノまたは固溶体が析出 している こ と を特徴と する構成 1 または 2 に記載の無機組成物又は結晶化ガラス。 4. The inorganic composition or crystallized glass according to constitution 1 or 2, characterized in that a crystallization day or a solid solution is precipitated.
(構成 4 ) 質里 % % %で、 (Configuration 4) At the mass%%%,
S i 〇 3 5 〜 6 5 % わよび S i ○ 3 5 〜 6 5%
A 1 a ο 5 〜 3 0 % び A 1 a ο 5 to 30% and
K 2 Ο 0 〜 2 5 % よび /または K 2 Ο 0 to 25% and / or
N a 2 ο 0 〜 2 5 % N a 2 ο 0 to 2 5%
の範囲の各成分を含有する と を特徴と 3 のレ、ずれ力 ¾ に記载の無機組成物又は 晶化ガラス And an inorganic composition or crystallized glass described in (3), displacement force ¾.
(構成 5 ) 量 %で、 (Configuration 5) With amount%,
P o および/または P o and / or
B o および または B o And or
Z o 0 〜 0 %、 および/または Z o 0-0%, and / or
T o 0 〜 5 %、 および Zまたは To 0 to 5%, and Z or
L i 2 O 0 〜 : 1 0 %、 および/または L i 2 O 0 to: 10%, and / or
M g O 0 〜 : 1 0 %、 および Zまたは M g O 0 to: 10%, and Z or
C a O 0 〜 : L 0 %、 および/または C a O 0 to: L 0%, and / or
Z n 〇 0 〜 : 1 0 %、 および Zまたは Zn 0 0 to: 10%, and Z or
S r O 0 〜 ; L 0 %、 および Zまたは S r O 0 to; L 0%, and Z or
O 0 0 O 0 0
だし M + C a O + Z n O + S r 〇 + B a O 0 2 0 % 、 ひ' ま を含有する と を特徴とする構成 4 に記載の無 晶化ガラ ス 。 However, the amorphized glass according to constitution 4, characterized in that it contains M + CaO + ZnO + SrO + BaO 0 20% and sunflower.
m m厚における光線透過率特性が 1 5 5 O n mにお で ¾5 Ό と を特徴とする、 構成 1 〜 5 の レ、ずれ力 こ 物又は結晶化ガラス The light transmission characteristics at 1 m thickness are 15 5 Onm and ¾5 mm, and the lasing force, misalignment force, or crystallized glass of configurations 1 to 5
成 1 〜 6 の う ちいずれか一の構成記載の無機組成物 ス を用レ、た光学デバィ ス 。 An optical device using the inorganic composition described in any one of the components 1 to 6.
成 1 〜 6 の う ちいずれか一の構成記載の無機組成物 ス を用レ、た光フ ィ ルタ用基板 An optical filter substrate using the inorganic composition described in any one of the constitutions 1 to 6
成 8 の光フ ィルタ用 ¾ に t β体多層膜が形成され とする光フ ィ ルタ An optical filter in which a tβ multilayer film is formed on the optical filter of Example 8
) 構成 1 〜 6 の う ちいずれ力 —の構成記載の無機組成 ィ匕ガラス を用いた人工 1ST ) Artificial 1ST using inorganic composition 匕 glass described in the composition of any one of composition 1 to 6
) 構成 1 〜 6 の う ちレ、ずれ力 一の構成記載の無機組成 ィヒガラス を用いた情報記録媒体用基板 ) Out of configurations 1-6, displacement force Information recording medium substrate using inorganic composition ighi glass described in one configuration
) 構成 1 6 の う ちレ、ずれ力 一の構成記載の無機組成 化ガラスを用いた電子回路基板。 An electronic circuit board using the inorganic composition glass described in the first configuration.
) 質量 %で ) Mass%
3 5 〜 6 5 % および Zまたは 2 〇 0 〜 2 5 %、 および /または 3 5 to 6 5% and Z or 2 0 to 25%, and / or
N a 2 Ο 0 〜 2 5 % 、 ねよび /または N a 2 Ο 0 to 25%, Nebi and / or
P 2 Ο 0 〜 1 0 % 、 ね よび Zまたは P 2 Ο 0 to 10%, ne and Z or
B 2 Ο 3 0 〜 1 5 % 、 および /または B 2 Ο 30--15%, and / or
Z r 〇 2 0 〜 1 0 % 、 および Zまたは Z r 0 20-10%, and Z or
T i Ο 2 0 〜 1 5 % 、 ねよび Zまたは T i Ο 2 0 ~ 1 5 %, Neyobi Z or
L i 2 Ο 0 〜 1 0 % 、 お び Zまたは L i 2 Ο 0 to 10%, and Z or
M g ο 0 〜 : L 0 %、 および /または M g ο 0 to: L 0% and / or
C a Ο 0 〜 : 1 0 %、 および /または C a Ο 0 to: 10%, and / or
Z n Ο 0 〜 1 0 %、 および /または Z n Ο 0 to 10%, and / or
S r ο 0 〜 ; 1 0 %、 およぴ /または S r ο 0 〜; 1 0%, and / or
B a ο 0 〜 1 0 %、 および Zまたは B a ο 0 to 1 0%, and Z or
ただし M g O + C a Ο + Z n O + s r o + B a O 0 〜 2 0 % 、 However, M g O + C a Z + Z n O + s r o + B a O 0 to 20%,
3oよび/または 3o and / or
S b 2 Ο 3 0 〜 1 % S b 2 Ο 3 0 to 1%
A 1 2 Ο 3 / 2 Oで表わされるモノレ比率が 1 以下、 A monore ratio represented by A 1 2 Ο 3/2 O is 1 or less,
ただし Rは L i 、 N a 、 κから選ばれる 1 種以上、 Where R is at least one selected from L i, N a and κ,
の範囲の組成を有する原料を 、 1 2 0 0 °C 〜 1 5 0 0 °Cで溶融し、 得られた母ガラ ス を、 5 0 0 。C 〜 7 5 0 °Cで結晶化する こ と を特徴 とする、 構成 1 〜 6 の いずれかに の挺ハ、、機組成物または結晶化ガ ラスの製造方法。 A raw material having a composition in the range of 1 ° C. to 1500 ° C. was melted at a temperature of 120 ° C., and the obtained mother glass was 5 0 0. Crystallization at C to 75 ° C., a method for producing a mechanical composition or crystallized glass according to any one of constitutions 1 to 6.
本発明は、 成分組成を質量 %で表 してレ、るため、 直接表せるべき ものではないが、 上記の構成と 同様の効果を奏する には、 モル%に て概ね以下の範囲と なる In the present invention, since the component composition is expressed in mass%, it should not be expressed directly. However, in order to achieve the same effect as the above configuration, the mol% is generally in the following range.
(構成 1 4 ) モル% で (Composition 14) in mol%
S i Ο 2 3 0 〜 5 5 0/ (。 、 及び S i Ο 2 3 0 to 5 5 0 / (., And
A 1 2 Ο 3 1 0 〜 4 0 % 、 及び、 A 1 2 Ο 3 1 0 to 40 0% and
2 ο 0 〜 2 5 % 、 及び /又は 2 ο 0 to 2 5% and / or
N a 2 Ο 0 〜 2 5 % 、 N a 2 Ο 0 to 25%,
の範囲の各成分を含有する こ と を特徴とする構成 1 〜 3 のいずれか に記載の無機組成物又は結晶化ガラス The inorganic composition or crystallized glass according to any one of configurations 1 to 3, characterized by containing each component in the range of
(構成 1 5 ) モル /o で 、 (Composition 15) at mol / o,
S i 〇 2 3 0 〜 5 5 0/ Ό 、 および S i ○ 2 3 0 to 5 5 0 / Ό, and
A 1 2 Ο a 1 0 〜 4 0 % 、 および A 1 2 Ο a 1 0 to 40%, and
K 2 ο 0 〜 2 5 % 、 よび Zまたは K 2 ο 0 to 25% and Z or
N a 2 Ο 0 〜 2 5 % ヽ よぴ /または N a 2 Ο 0 to 25% ヽ Yoppi / or
Ρ 2 〇 0 〜 1 0 % 、 および Zまたは Ρ 2 0-10%, and Z or
Β 2 Ο 3 0 〜 1 0 % 、 お よび /または Β 2 Ο 30--10% and / or
Ζ r 〇 2 0 〜 1 0 % 、 および Zまたは Ζ r 0 20-10%, and Z or
T o _ 0 〜 1 5 % 、 および Zまたは T o _ 0 to 15%, and Z or
L 2 〇 0 〜 2 0 % 、 および/または L 2 0 to 20%, and / or
M o 0 〜 1 0 %、 および または M o 0 to 10%, and or
C o 0 〜 : 1 0 %、 および/または C o 0 to: 10%, and / or
Z o 0 〜 1 0 %、 および または Z o 0 to 10%, and or
S r O 0 〜 : L 0 %、 および Zまたは S r O 0 to: L 0% and Z or
B a O 0 〜 1 0 %、 およびノまたは B a O 0-10%, and no or
ただし M g O + C a 〇 + Z n O + S r O + B a 〇 0 〜 1 5 %、 お ょぴ Zまたは However, MgO + C a 〇 + Z n O + S r O + B a 〇 0 to 15%, O Z or
S b 2 O 0 〜 0 . 5 % T/JP2006/314825 高レ、熱膨張係数を示す 機組成物を作製するためには、 組成につレ、 て 、 A 1 o 成分 、 R o成分 、 ただし Rは L i 、 Kおよび N a から選ばれる少な < と も 1種以上、 を含有し、 A 1 2 O / z R ο で表わされるモ ノレ比率が 1 以下である こ と が必須でめる 更に好ま し < は A 1 O R oで表わされるモ ノレ比率が 0 . 8 以下であ り 、 最も好ま し く は 0 5 以下である。 これを越える と 、 ガラス溶 融 曰 S b 2 O 0 to 0.5% T / JP2006 / 314825 In order to produce a machine composition that exhibits a high thermal expansion coefficient, A1o component, Ro component, where R is from Li, K, and Na It is essential that at least one selected <contains at least one, and the mole ratio represented by A 1 2 O / z R ο is 1 or less. The monore ratio represented is 0.8 or less, most preferably 0.5 or less. Beyond this, glass melting
皿度や結晶化処理 in曰n.度を高く しなければな らず 、 溶融性が低下 し て しま 5 The degree of dishing and crystallization in 処理 n.degree must be increased and meltability is reduced.
また 、 本発明の無機組成物は金属ゃ有機物と の 膨張係数におけ るマ クチングが良好である 。 それを端的に表せば 、 2 5 °Cに ける 料の長さ をし 、 T°C ί'こおける試料の長さ をしと した時、 In addition, the inorganic composition of the present invention has good matching in terms of expansion coefficient with metal or organic matter. In short, the length of the sample at 25 ° C and the length of the sample at T ° C
曰度 T につレ、て d ( Τ ) / d T = ( 1 / L ) X ( d L / d T D (Τ) / d T = (1 / L) X (d L / d T
) で表わされる d a ( T ) / d T の値が、 ― 3 0 C 〜 7 0 °Cの温 度 TO囲に レ、て常に 0 以上 、 よ り 好ま し く は 0 を越える特性を示 し てお り 、 その上、 5 0 °C 〜 3 0 0 °Cの温度範囲においてち d a (), The value of da (T) / dT is always greater than or equal to 0 in the temperature TO range of -30 ° C to 70 ° C, more preferably more than 0. Furthermore, in the temperature range of 50 ° C to 300 ° C, da (
Τ ) / d T の値は常に 0 以上、 よ り 好ま し く は 0 を越える特性を示 -— で 、 本発明の 機組成物は 、 ガラス、 お びセラ 、 , 、ノ、 ク ス 、 結晶化ガラス等であ り 、 特 結 曰 Τ) / d T always has a value of 0 or more, more preferably more than 0-, and the machine composition of the present invention is made of glass, sera, Specialized glass, etc.
曰曰化ガラ ス であ る と が好ま しい。 結晶化ガラスは、 旦溶解成形したガラスに再び熱処理を行 う こ と でガラス內部に所望の結 曰 It is preferable that the glass is hatched. The crystallized glass is subjected to a heat treatment again on the glass that has been melt-molded, so that a desired crystal can be formed on the glass wall.
曰曰を析出 させる方法に ぶ て得られる もの であ り 、 こ の方法が 、 ガラス內部に空孔等の欠陥を作る こ と な < 百 的物の作製が可能と なるからである。 This is because it can be obtained by a method for depositing soot, and this method makes it possible to produce a <100% material that creates defects such as vacancies in the glass soot.
また 、 本発明の 機組成物は N a K x A 1 S i OThe mechanical composition of the present invention is Na K x A 1 S i O.
、 ただ し 0 < X ≤ 4 、 であ 曰 , Where 0 <X ≤ 4, and
る結 B曰及び Z又は固溶体が析出 している と が 、 本発明の 百 的の つである熱膨張係数が 曰 As a result, the thermal expansion coefficient that is one of the hundreds of the present invention is
1im.度の上昇に対し て比例的に増加する物性を得るために好ま し く 、 X = 4 である力ノレ シラィ 卜及び /又は力ルシラィ 卜 固溶体が析出 してレ、る ·>· と が上記 物性を得るためにぶ 好ま しレヽ 尚、 カノレシラィ 卜 ( κ A 1 S i 〇 It is preferable to obtain a physical property that increases proportionally with an increase in the degree of 1im., And that X = 4 force stress 卜 and / or force lucy 固 solid solution is precipitated. In order to obtain the above physical properties, it should be noted that canore silly 卜 (κ A 1 S i 〇
) は別名力 リ フ ォルラィ 卜 と も呼ばれるが、 以下文章には力ルシ ラィ 卜 と して Bd载する ) Is also known as power reform ラ, but in the text below, it will be written as power シ
更にヽ 本発明の 機組成物は 、 平均線膨張係数が 3 0 °C 7 0Cの *曰 Further, the machine composition of the present invention has an average linear expansion coefficient of 30 ° C 70 ° C.
恤度範囲におレ、て 、 6 0 X 1 0 - 7 /。 〜 1 5 0 X 1 0 - 7 /恤度range me Te,, 6 0 X 1 0 - 7 /. ~ 1 5 0 X 1 0 - 7 /
°Cで - ある と を特徴とする た 、 0 °C 〜 2 0 0 °Cの温度範囲にお レヽて 7 0 X 1 0 - / C 1 6 0 X I 0 - 7 ノでである , と を特徴° In C - other, wherein when there, 0 ° C ~ 2 0 0 0 ° 7 Te Contact Rere a temperature range of C X 1 0 - / C 1 6 0 XI 0 - is at 7 Bruno, a city Characteristic
― と し 、 2 0 0 °C 〜 3 0 0 °Cの温度範囲において 8 0 X 1 0 / °C― In the temperature range of 200 ° C to 300 ° C, 80 X 10 / ° C
〜 1 8 0 X 1 0 一 / °Cである と を特徴とする , ~ 1 80 X 1 0 1 / ° C,
次に原ガラスの組成 囲を限定する理由について以下に述ベる。 以下 、 成分の含有量につレ、ては特に明記しない限 り は質量 %によつ て記载する S i o 成分は、 原ガラ ス の熱処理に よ り 、 主 晶相 と して析出する N a ― x A 1 S i 4 O 、 ただし 0 ≤ XNext, the reason for limiting the composition range of the original glass will be described below. Hereinafter, unless otherwise specified, the S io component written in mass% is precipitated as the main crystal phase by heat treatment of the original glass. a ― x A 1 S i 4 O, where 0 ≤ X
< 4 、 である結晶及び /又は固溶体、 と り わけ力ルシラィ 卜 を構成 する極めて重要な成分である。 含有量の下限と しては、 3 5 % ではガラス にな り に < レ、 、 3 5 %が好ま し く 、 3 8 %がよ り 好ま し < 、 4 0 %が最も好ま しい。 含有量の上限は 6 5 %を越える と原 ガラスの粘性增加にぶ り ヽ 溶融 、 成形性が困難になる為 6 5 %が好 ま し < 、 5 5 %がよ 好ま し く 、 5 0 %が最も好ま しい <4, is a very important component of the crystal and / or solid solution, especially the power of the lucifer 卜. As the lower limit of the content, 35% is less preferable than glass, and 35% is preferable, 38% is more preferable, and 40% is most preferable. If the upper limit of the content exceeds 65%, the viscosity of the original glass will increase, and melting and formability will be difficult. 65% is preferred <, 55% is preferred, 50% Is most preferred
A 1 O 成分も ヽ s i O 2 成分と 同様、 主 曰 A 1 O component is the same as ヽ si O 2 component.
曰曰相を構成する極 めて重要な成分であるが 、 その Mが 5 %未満では所望の結晶相が得 0 %がよ り 好ま し く 2 %が最も好ま し また、 3 0 %を越え る と原ガラ スの粘性増加によ り 成形性が こなる為、 上 は 3 0 %が好ま し く 、 2 5 %力 よ り 好ま し く 、 2 0 %が最も好ま し Although it is a very important component constituting the liquid phase, if its M is less than 5%, a desired crystal phase can be obtained. 0% is more preferable, 2% is most preferable, and if it exceeds 30%, the moldability is degraded due to an increase in the viscosity of the original glass, so the upper is preferably 30%. 5% better than force, 20% most preferred
B 2 O 成分は、 ガラ ス 性を向上させる為に有効な成分であ り 任意に する こ と ができ るが、 含有 の增加はガラス構造の安 定化を引 き起こすこ と と な り 、 熱処理によ る ガラス内部への結晶相 析出が こなる。 よって、 所望の析出結晶相が変化 しな The B 2 O component is an effective component for improving the glass property and can be arbitrarily set.However, the increase in the content causes stabilization of the glass structure. Crystal phase precipitation inside the glass due to heat treatment. Therefore, the desired precipitated crystal phase does not change.
て含有する こ と が可能であ り 、 その量の上限は 1 5 %が好ま し よ り 好ま し く は 0 %であ り 、 最も好ま し く は 5 %である The upper limit of the amount is 15%, preferably 0%, most preferably 5%.
P 2 O 5 成分は、 析出結晶の核形成に寄与する任意成分であるが 過度に加える と ガラス化が こな る。 よ っ てその の上限はThe P 2 O 5 component is an optional component that contributes to the nucleation of precipitated crystals, but vitrification occurs when added excessively. So the upper limit of that is
0 %が好ま し よ り 好ま し く は 5 %である 0% is more preferable than 5%
Z r O 2 成分は、 析出結晶の 機 gする その上、 析出 結 SBの微細化と材料の機械的強度向上な らびに化学的 久性の向上 顕著な効果を有する任意成分である が 過剰に加える と 、 原ガラ ス の溶融が困難にな り 、 ガラス溶融時に Z S i O 等の溶け残 り が発生 しやすく なる。 も し く は 結晶化処理後に Z r O 2 が析出 し て しま う 。 よ っ て、 その量の上 は 1 0 %が好ま しい。 よ り 好ま し く は、 8 %であ り 、 最も好ま しく は 6 %である。 Z r O 2 component, on which the machine g of precipitated crystals, precipitation binding SB of but an optional component in excess with improved pronounced effect of chemical durability and mechanical strength improvement rabbi miniaturization and materials If it is added, it becomes difficult to melt the original glass, and ZS i O or the like is likely to be left behind when the glass is melted. Or, ZrO 2 will precipitate after the crystallization process. Therefore, 10% is preferable above the amount. More preferred is 8%, most preferred is 6%.
T i O 2 成分は、 析出結晶の核剤 と して機能する任意成分である その上、 析出結晶の 化 と材料の 度向上な らぴに化学 久性の向上に顕著な効果を示す成分であるが こ加える と 原ガラ ス の が こなる、 も し く は 晶化 に T i 〇 過理 The TiO 2 component is an optional component that functions as a nucleating agent for precipitated crystals. In addition, it is a component that has a remarkable effect on improving the chemical properties as well as the formation of precipitated crystals and the improvement of the degree of material. If added, the original glass will be damaged, or T i 〇
が析出 して しま う。 Will precipitate.
よ って、 その量の上限は 1 5 %が好ま し よ り 好ま し く は 1 0 % であ り 、 最も好ま し く は 6 %である Therefore, the upper limit of the amount is preferably 15%, more preferably 10%, and most preferably 6%.
L i 2 O成分は、 原料の溶 S 反応を助長させ、 ガラス 温度を 下させる上で効果的な成分であるが、 含有 を増加させる と析出 結晶相の変化、 化学的耐久性の悪化を引 き起こす。 よ っ て、 その量 の上限は、 1 0 %が望ま し よ り 好ま し く は .8 %であ り 、 最も好 ま しく は 5 %である。 本成分は任意に含有させる こ と ができ る成分 である が、 下限と してよ り 好ま し く は 1 %であ り 、 最も好ま しく はThe Li 2 O component is an effective component in promoting the dissolution S reaction of the raw material and lowering the glass temperature, but increasing the content causes a change in the precipitated crystal phase and deterioration in chemical durability. Wake up. Therefore, the upper limit of the amount is preferably 10%, more preferably 0.8%, and most preferably 5%. This component can be optionally added, but the lower limit is more preferably 1%, and most preferably
2 %である。 2%.
K 2 Ο成分及ぴ Ν O成分は N K x A 1 4 S i , OK 2 Οcomponent and Ν O component is NK x A 1 4 S i, O
0 ≤ X ≤ 4 ) である結晶及び Ζ又は固溶体を析出 させるために は少な く と も どち ら力: の成分を含有しなければな らない。 In order to precipitate crystals and soot or solid solutions with 0 ≤ X ≤ 4), at least one of the components must be included.
Κ 2 Ο成分は、 原ガラ ス の こ よ り 、 主結晶相 と て祈出す る結晶相を構成する成分の つである と 同時に ガラスの粘性向 上にも寄与する成分である ただし、 過度の含有はガラスの化学的 久性を悪化させて しま う ため、 含有 の上限は 2 5 %が好ま し くΚ 2 Ο components, raw glass Ri I scan this, which is the main crystalline phase and the component contributing also on the viscosity propensity of glass crystal phase and the is One of the components constitute at the same time that put out prayer Te However, excessive Since the content will deteriorate the chemical durability of the glass, the upper limit of content is preferably 25%.
2 3 %が よ り 好ま し く 、 2 0 %が最も好ま し こ X = 4 であ るカルシライ ト及び/又はカルシライ ト 固溶体を結晶 と して析出 さ せる為には必須成分であ り 、 こ の結晶相を得るた めの含有 の下 は 1 0 %を超える事が好ま し く 2 %がよ り 好ま し く 5 %が 最も好ま しい。 23% is more preferred, 20% is most preferred X = 4 is an essential component for precipitating calcite and / or calcite solid solutions as crystals. Under the content for obtaining a crystalline phase, it is preferable to exceed 10%, 2% is more preferable, and 5% is most preferable.
N a 2 O成分は、 原ガラ ス の熱処理によ り 、 主結晶相 と して析出 する結晶相を構成する成分の一つである と 同時に溶融ガラ ス の粘性 向上に も寄与する成分である。 ただし過度の含有はガラスの化学的 JP2006/314825 向上にも寄与する成分でめる ο ただ し過度の含有はガラ ス の化学的 耐久性が悪化させて しま う ため 含有量の上限は 2 5 %が好ま し く 1 6 %がよ り 好ま し < 1 0 %未満が琅も好ま しい。 また aThe Na 2 O component is one of the components constituting the crystal phase that precipitates as the main crystal phase by heat treatment of the original glass, and at the same time contributes to the improvement of the viscosity of the molten glass. . However, excessive content is chemical of glass JP2006 / 314825 A component that also contributes to improvement ο However, excessive content will deteriorate the chemical durability of glass, so the upper limit of content is preferably 25%, preferably 16% More preferred <10% is preferred. Also a
4 一 K x A 1 4 S i 4 o 1 6 ( X 4 ) である力ルシラィ ト及び4 1 K x A 1 4 Si 4 o 1 6 (X 4)
/又は力ノレシラィ h 固溶体を 晶 と して析出 させる為に a 2 O 成分の ¾有直の上限は 5 %が好ま し < 、 含有 しなレ、こ と がよ り 好まFor the purpose of precipitating the solid solution as crystals, the upper limit of the a 2 O component is preferably 5% <, and it is more preferred that it is not contained.
] ヽ ] ヽ
し レ、 o Les, o
M g 〇 C a O S r o B a O Z n O成分は 、 溶融ガラ ス の 粘性向上ゃ析出結晶の微細化のために有効な任音成分である 。 ただ し、 過剰に加える と 析出結 H The MgOCaSORoBaOZnO component is an effective component for improving the viscosity of molten glass and for refining precipitated crystals. However, if excessively added, precipitation H
曰曰相の変化、 ガラ ス形成能の低下と い つた悪影響を引 き起 しやす < なるため、 各成分の含有量の上限は The upper limit of the content of each component is less likely to cause adverse effects such as changes in the phase of the rice and reduction in the ability to form glass.
1 0 %である と が好ま しい o また これら各成分の合計量の上限 は 2 0 %である こ と が好ま し < よ り 好ま し く は 1 0 %であ り 、 更 に好ま し く は 5 %である o 10% is preferred o The upper limit of the total amount of each of these components is preferably 20% <more preferably 10%, and even more preferably 5% o
また 、 素材の物性を損なわない範囲で、 ラ ンタ ノ ィ ド、化合物及ぴ In addition, as long as the physical properties of the material are not impaired, lanthanides, compounds and
S n O C u O N i O F e 2 o 3 c e O M n 〇 V 2 O 5 N b 2 O 5 T a 2 O 5 W O 3 M o O , B i 2 〇 3 G e O 2 ヽ a 2 O 3 成分を合計で 2 0 %まで含有させる こ と が出来 る。 S n OC u ON i OF e 2 o 3 ce OM n ○ V 2 O 5 N b 2 O 5 Ta 2 O 5 WO 3 Mo o, Bi 2 ○ 3 G e O 2 ヽ a 2 O 3 Component Up to 20% in total.
S b 2 O 3 成分は 、 ガラス の清透剤 と して添加 し得るが、 含有量 の上限は 1 %で充分である ο 上限と して よ り 好ま しく は 0 . 5 %で あ り 、 さ らに好ま し く は 0 2 %である The Sb2O3 component can be added as a glass clearing agent, but the upper limit of content is 1%. Ο The upper limit is more preferably 0.5%. More preferred is 0 2%
A s 2 O 3 ぴ P b O成分は、 環境上好ま し く ない成分である ため、 使用を極力控えるベさでめ る 。 As s 2 O 3 and P b O components are unfavorable for the environment, so use them as much as possible.
次に 、 本発明にかかる無機組成物の製造方法の一 つは、 上記の組 成を熔解 し 成形 除冷を行つた後、 更 ;To晶相析出の為の熱処理 を行 う o Next, one of the methods for producing the inorganic composition according to the present invention is to melt the above-described composition, perform forming and cooling, and then perform heat treatment for To crystal phase precipitation o
実施例 Example
本発明の好適な実施例につレ、て説明する。 A preferred embodiment of the present invention will be described.
表 1 〜表 5 は本発明 の無機組成物の実施例 ( N o . :! 〜 2 3 ) 及 び従来発明 B Tables 1 to 5 show examples of inorganic compositions of the present invention (No .:! To 23) and conventional invention B.
PPの 機組成物 (比較例 1 2 ) について、 組成の他に About the machine composition of PP (Comparative Example 1 2)
、 ガラス の 'ロ 曰 The glass of 'Ro 曰
B曰化慨 一 3 0 C 〜 7 0 °C よび 0 °C 〜 2 0 0 °C 2 0 0 °C 〜 3 0 0 に ける平均熱膨張係数 1 5 5 0 n mにお ける 1 m m厚の光線透過率 析出結晶相 A 1 2 O a / R 2 〇 のモ ル比率 d a ( T ) / d t を示したものである。 比較例 1 は結晶 化ガ ラ ス 、 比較例 2 はァモルフ ァ ス ガ ラ ス で あ る ο B Incubation Average Coefficient of Thermal Expansion at 30 ° C to 70 ° C and 0 ° C to 20 ° C, 20 ° C to 30 ° C, 1 mm thickness at 1550 nm Light transmittance This shows the mole ratio da (T) / dt of the precipitated crystalline phase A 1 2 O a / R 2 0. Comparative Example 1 is crystallized glass and Comparative Example 2 is amorphous glass.
上記実施例のガラス の製造方法を説明する ο 酸化物、 炭酸塩、 硝 酸塩の原料を混 Π し 、 これを通常の熔解装置を用いて約 1 2 0 0 °C The method for producing the glass of the above embodiment will be described. Ο Oxide, carbonate, and nitrate raw materials are mixed, and this is mixed using a normal melting apparatus.
〜 1 5 0 0 C の -) B ~ 1 5 0 0 C-) B
Um.度で熔解し 攪拌、 均質化 した後、 成形 , 冷却ェ 程を経てガラス成形体を得た o その後、 これを 5 0 0 °C 〜 6 0 0 °C にて 1 〜 1 0 時間熱処理して結晶核形成後、 5 5 0 °C 〜 7 5 0 °Cに て 1 〜 1 0 時間熱処理結晶化して、 所望の無機組成物を得た。 After melting at Um. Degree, stirring and homogenizing, glass forming body was obtained through molding and cooling process o After that, it was heat-treated at 500 to 600 ° C for 1 to 10 hours After the formation of crystal nuclei, heat treatment was performed at 55 ° C. to 75 ° C. for 1 to 10 hours to obtain a desired inorganic composition.
析出 fcfc H Precipitation fcfc H
7Γ'Β 5曰相は X線回折装置 ( フ ィ リ ツプス社製 、 商品名 : X ' P e r t 一 Μ P D ) 及ぴェネルギ一分散型分析装置 (日 立製作所製、 商品名 S 一 4 0 0 0 N 堀場製作所製 、 商 π 名 E X 4 2 0 )で 同 疋' した。 7Γ'Β 5 曰 相 is an X-ray diffractometer (manufactured by Phillips Co., Ltd., trade name: X'Pert Ichi PD) and an energy analyzer with a single dispersion (manufactured by Hitachi, Ltd., trade name S 1 40) 0 0 N HORIBA, Ltd., quotient π name EX 4 2 0).
線膨張係数の測定は、 熱膨張計 (マ ツ クサィェンス 社製、 商品名 T D 5 0 0 0 S ) を用いて測疋 し 7こ。 s 料は 直径 5 m m、 お The linear expansion coefficient was measured using a thermal dilatometer (manufactured by Macintosh, trade name: T D 5 0 0 0 S). s Fee is 5 mm in diameter,
2 0 m m の円柱状に力卩ェし 皿曰度範囲は一 5 0 Cから 3 2 0 °C、 昇 温速度は 4 °C / m i n . に設定し、 温度一伸びの関係を示す膨張曲 線から算出 した。 The force is applied to a 20 mm cylinder, and the temperature range is from 150 ° C to 320 ° C. The temperature rate was set to 4 ° C / min. And calculated from the expansion curve showing the relationship between temperature and elongation.
透 rn過率は 、 1 m m厚に両面研磨された試料を用い、 分光光度計 ( 日 立 i製一作所製、 商品名 : U — 4 0 0 0 ) を用いて測定 した。 表 1 The transmittance was measured using a spectrophotometer (manufactured by Nissho i-Isakusho Co., Ltd., trade name: U-400) using a sample polished on both sides to a thickness of 1 mm. table 1
mass% 実施例 1 実施例 2 実施例 3 実施例 4 実施例 5 mass% Example 1 Example 2 Example 3 Example 4 Example 5
Si02 43.8 43.0 46.0 42.0 46.3 Si0 2 43.8 43.0 46.0 42.0 46.3
Al203 30.0 27.0 27.0 18.0 15.0 Al 2 0 3 30.0 27.0 27.0 18.0 15.0
P205 P 2 0 5
B203 5.0 B 2 0 3 5.0
Zr02 3.0 3.0 Zr0 2 3.0 3.0
Li20 4.0 4.8 4.8 4.8 4.8 Li 2 0 4.0 4.8 4.8 4.8 4.8
K20 19.0 19.0 19.0 19.0 21.0 K 2 0 19.0 19.0 19.0 19.0 21.0
Na20 Na 2 0
MgO MgO
ZnO 3.0 3.0 3.0 3.0 3.0 ZnO 3.0 3.0 3.0 3.0 3.0
BaO BaO
SrO SrO
Sbz03 0.2 0.2 0.2 0.2 0.2 Sb z 0 3 0.2 0.2 0.2 0.2 0.2
Ti02 2.0 3.7 Ti0 2 2.0 3.7
Gd203 3.0 3.0 3.0 Gd 2 0 3 3.0 3.0 3.0
100.0 100.0 100.0 100.0 100.0 結晶化温度 (°c) 680 680 720 660 660 100.0 100.0 100.0 100.0 100.0 Crystallization temperature (° c) 680 680 720 660 660
GTE (10"7/°C) 103 108 106 108 110 GTE (10 " 7 / ° C) 103 108 106 108 110
(-30〜70°C) (-30 ~ 70 ° C)
114 118 113 117 119 114 118 113 117 119
128 131 130 132 134 透過率 90.2 90.3 90.3 90.5 90.3 128 131 130 132 134 Transmittance 90.2 90.3 90.3 90.5 90.3
(1550nm, 1mmt) 結晶相 KAISi04 (1550nm, 1mmt) Crystal phase KAISi0 4
Al203/R20 Al 2 0 3 / R 2 0
0.88 0.73 0.73 0.49 0.38 0.88 0.73 0.73 0.49 0.38
(モル比率) da (T) /dt >0 (- 50〜300°C) (Molar ratio) da (T) / dt> 0 (-50 to 300 ° C)
6 314825 5 6 314825 5
実施例の温度一熱膨張係数曲線よ り d α (τ) Z d t を確認 した と ろ、 全ての実施例において、 一 5 0 °C 〜 3 0 0 °Cの温度範囲にお て d a (T ) Z d t が 0 以上である こ と を確認した。 The d α (τ) Z dt was confirmed from the temperature-coefficient of thermal expansion curve of the examples, and in all examples, da (T in the temperature range of 50 ° C to 300 ° C. ) It was confirmed that Z dt was 0 or more.
尚、 当発明の無機組成物は、 組成のみでな く 、 結晶化温度によ り : 線材板な膨張 と透過率の が可能である えば、 結 相が変化 1 ない 定する こ と に 多料、 範囲にて結晶化温度および/または時間を長く 設 The inorganic composition of the present invention depends not only on the composition but also on the crystallization temperature. : If the wire plate is capable of expansion and transmittance, the crystallization temperature and / or time can be set long in a wide range of conditions to determine the phase does not change.
よ り 透過率の値は悪化する 張 の値を増加 させる こ と 層該と The transmittance value gets worse. The tension value is increased.
ができ る。 You can.
膜基し Membrane-based
また、 結晶相が析出可能な範 度および/または時 板てと In addition, the range in which the crystalline phase can precipitate and / or the time plate
を短く 設定好のにする こ と によ り の値は結晶化処理時間の 少に伴 透過率の The value obtained by shortening and setting the value of the
誘相適く なる 方 を良化させる こ と ができ る 産業上の利用可能性 Can improve the person who is suitable for the invitation phase Industrial applicability
性電で On the electricity
当発明の無機組成 は そ の平均熱 張係 よ り 、 金属や有 The inorganic composition of the present invention is based on its average thermal tension, and it is a metal or organic material.
体をあ Body
と の複合材料を作る上で有益である えば If it is useful in making composite materials with
求多る Demand
層為め Stratification
膜、ら Membrane
れ本カ Remoto
。 また、 熱膨張係数の値が温発形度 、 に対して安定した挙動を示すため その他光学材料、 例えば、 温度成補か明償用部材にも好適である。 . In addition, since the value of the thermal expansion coefficient shows a stable behavior with respect to the warming degree, it is also suitable for other optical materials, for example, temperature compensation or compensation members.
カロえて、 高い熱膨張係数を持ち つ つのる こ と 力: ら、 金属 と のマ ッチング し It has a high coefficient of thermal expansion and has the power to: match with metal
が求め られる人工歯冠にも好適であ透無たり 、 方、 記 用基 、 電子回路基板と しても使用可能であ過機光る It is also suitable for artificial dental crowns that are required to be transparent, but can also be used as electronic circuit boards.
組率フ Group rate
特成ィ Special
性物ル 、 Sexuality,
光のかタ Light
学高をら From school
得光フさ Gain light
をフィる Fill
ル必事ィ Le Necessary
要ルがタ In short
でのタと す用きよ 基るるつ > Use it in your base rut>
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2005213816A JP5173123B2 (en) | 2005-07-25 | 2005-07-25 | Inorganic composition |
| JP2005-213816 | 2005-07-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2007013538A1 true WO2007013538A1 (en) | 2007-02-01 |
Family
ID=37683429
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2006/314825 Ceased WO2007013538A1 (en) | 2005-07-25 | 2006-07-20 | Inorganic composition |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JP5173123B2 (en) |
| WO (1) | WO2007013538A1 (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103803803A (en) * | 2014-03-08 | 2014-05-21 | 曹小松 | High-strength glass-ceramic and its preparation method |
| CN103819093A (en) * | 2014-03-08 | 2014-05-28 | 曹小松 | Technology of preparing glass-ceramic by sintering method and glass-ceramic with high flatness |
| CN103819089A (en) * | 2014-03-08 | 2014-05-28 | 曹小松 | Technology of preparing glass-ceramic by melting method and glass-ceramic with high flatness |
| WO2016138330A1 (en) * | 2015-02-26 | 2016-09-01 | Corning Incorporated | Fast ion-exchangeable boron-free glasses with low softening point |
| WO2018040749A1 (en) * | 2016-08-30 | 2018-03-08 | 深圳顺络电子股份有限公司 | Low temperature co-fired ceramic material and preparation method therefor |
| CN108409147A (en) * | 2018-05-28 | 2018-08-17 | 河北省沙河玻璃技术研究院 | Devitrified glass and reinforcing devitrified glass applied to 5G communication mobile terminal protecgulums |
| CN108558216A (en) * | 2018-05-28 | 2018-09-21 | 河北省沙河玻璃技术研究院 | A kind of devitrified glass and chemical strengthening devitrified glass and its application |
| CN108640520A (en) * | 2018-05-28 | 2018-10-12 | 河北省沙河玻璃技术研究院 | Devitrified glass and reinforcing devitrified glass applied to 5G communication mobile terminal rear covers |
| US10179749B2 (en) | 2016-08-30 | 2019-01-15 | Shenzhen Sunlord Electronics Co., Ltd. | Low-temperature co-fired ceramic material and preparation method thereof |
| WO2020231963A1 (en) * | 2019-05-16 | 2020-11-19 | Corning Incorporated | Steam strengthenable glass compositions with low phosphorous content |
| US11214510B2 (en) | 2017-11-17 | 2022-01-04 | Corning Incorporated | Water-containing glass-based articles with high indentation cracking threshold |
| US11339084B2 (en) | 2020-05-12 | 2022-05-24 | Corning Incorporated | Fusion formable and steam strengthenable glass compositions with platinum compatibility |
| US11370696B2 (en) | 2019-05-16 | 2022-06-28 | Corning Incorporated | Glass compositions and methods with steam treatment haze resistance |
| US11767258B2 (en) | 2018-11-16 | 2023-09-26 | Corning Incorporated | Glass compositions and methods for strengthening via steam treatment |
| US12122711B2 (en) | 2019-05-16 | 2024-10-22 | Corning Incorporated | Steam strengthenable glass compositions with low phosphorous content |
| US12404204B2 (en) | 2019-05-16 | 2025-09-02 | Corning Incorporated | Glasses with modified young's modulus profile |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4467597B2 (en) * | 2007-04-06 | 2010-05-26 | 株式会社オハラ | Inorganic composition article |
| JP5072657B2 (en) | 2008-03-05 | 2012-11-14 | 株式会社松風 | Color tone adjusting composition for aluminosilicate glass and ceramic crown ceramics |
| CN103896486B (en) * | 2014-03-08 | 2016-07-13 | 安徽万佳节能科技有限公司 | Red stone-like glass-ceramic and preparation method thereof |
| JP6493653B2 (en) * | 2014-05-27 | 2019-04-03 | 日本電気硝子株式会社 | Temperature compensation member and optical device for optical communication using the same |
| JP7296306B2 (en) * | 2019-11-27 | 2023-06-22 | 株式会社オハラ | Glass-ceramics for optical filters and optical filters |
| JP7770811B2 (en) * | 2020-08-31 | 2025-11-17 | 株式会社オハラ | Glass-ceramics for optical filters and optical filters |
| JP7721348B2 (en) * | 2020-08-31 | 2025-08-12 | 株式会社オハラ | Inorganic composition with high thermal expansion coefficient |
| WO2022045062A1 (en) * | 2020-08-31 | 2022-03-03 | 株式会社 オハラ | Inorganic composition having high thermal expansion coefficient, crystallized glass for optical filter, and optical filter |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5331716A (en) * | 1976-09-03 | 1978-03-25 | Wada Seimitsu Shiken | Enamel for dentist |
| JPS6331421B2 (en) * | 1983-05-30 | 1988-06-23 | Nippon Electric Glass Co | |
| JPH1036137A (en) * | 1996-03-12 | 1998-02-10 | Jeneric Pentron Inc | Two phase ceramic material composition for dentistry |
| WO2002096818A1 (en) * | 2001-05-29 | 2002-12-05 | Asahi Glass Company, Limited | Crystallized glass for optical filter substrate and optical filter |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6331716A (en) * | 1986-07-28 | 1988-02-10 | 松下電工株式会社 | Method of working artificial stone and natural stone |
| JPH07277791A (en) * | 1994-03-31 | 1995-10-24 | Tdk Corp | Ceramic composition for insulating base and ceramic multilayer wiring circuit board |
| JP4736207B2 (en) * | 2001-03-08 | 2011-07-27 | 旭硝子株式会社 | Crystallized glass for optical filter substrate and optical filter |
-
2005
- 2005-07-25 JP JP2005213816A patent/JP5173123B2/en not_active Expired - Lifetime
-
2006
- 2006-07-20 WO PCT/JP2006/314825 patent/WO2007013538A1/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5331716A (en) * | 1976-09-03 | 1978-03-25 | Wada Seimitsu Shiken | Enamel for dentist |
| JPS6331421B2 (en) * | 1983-05-30 | 1988-06-23 | Nippon Electric Glass Co | |
| JPH1036137A (en) * | 1996-03-12 | 1998-02-10 | Jeneric Pentron Inc | Two phase ceramic material composition for dentistry |
| WO2002096818A1 (en) * | 2001-05-29 | 2002-12-05 | Asahi Glass Company, Limited | Crystallized glass for optical filter substrate and optical filter |
Cited By (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103819093A (en) * | 2014-03-08 | 2014-05-28 | 曹小松 | Technology of preparing glass-ceramic by sintering method and glass-ceramic with high flatness |
| CN103819089A (en) * | 2014-03-08 | 2014-05-28 | 曹小松 | Technology of preparing glass-ceramic by melting method and glass-ceramic with high flatness |
| CN103819089B (en) * | 2014-03-08 | 2016-01-06 | 启东远洋电缆有限公司 | Technology of preparing glass-ceramic by melting method and glass-ceramic with high flatness |
| CN103819093B (en) * | 2014-03-08 | 2016-01-20 | 启东斯单珂工具制造有限公司 | Technology of preparing glass-ceramic by sintering method and glass-ceramic with high flatness |
| CN103803803B (en) * | 2014-03-08 | 2016-05-25 | 曹小松 | High-strength glass-ceramic and its preparation method |
| CN103803803A (en) * | 2014-03-08 | 2014-05-21 | 曹小松 | High-strength glass-ceramic and its preparation method |
| WO2016138330A1 (en) * | 2015-02-26 | 2016-09-01 | Corning Incorporated | Fast ion-exchangeable boron-free glasses with low softening point |
| US10315949B2 (en) | 2015-02-26 | 2019-06-11 | Corning Incorporated | Fast ion-exchangeable boron-free glasses with low softening point |
| US10179749B2 (en) | 2016-08-30 | 2019-01-15 | Shenzhen Sunlord Electronics Co., Ltd. | Low-temperature co-fired ceramic material and preparation method thereof |
| WO2018040749A1 (en) * | 2016-08-30 | 2018-03-08 | 深圳顺络电子股份有限公司 | Low temperature co-fired ceramic material and preparation method therefor |
| US11643356B2 (en) | 2017-11-17 | 2023-05-09 | Corning Incorporated | Water-containing glass-based articles with high indentation cracking threshold |
| US11214510B2 (en) | 2017-11-17 | 2022-01-04 | Corning Incorporated | Water-containing glass-based articles with high indentation cracking threshold |
| US12054423B2 (en) | 2017-11-17 | 2024-08-06 | Corning Incorporated | Water-containing glass-based articles with high indentation cracking threshold |
| US11760685B2 (en) | 2017-11-17 | 2023-09-19 | Corning Incorporated | Water-containing glass-based articles with high indentation cracking threshold |
| US11377386B2 (en) | 2017-11-17 | 2022-07-05 | Corning Incorporated | Water-containing glass-based articles with high indentation cracking threshold |
| CN108558216B (en) * | 2018-05-28 | 2021-08-10 | 河北省沙河玻璃技术研究院 | Microcrystalline glass, chemically strengthened microcrystalline glass and application of chemically strengthened microcrystalline glass |
| CN108558216A (en) * | 2018-05-28 | 2018-09-21 | 河北省沙河玻璃技术研究院 | A kind of devitrified glass and chemical strengthening devitrified glass and its application |
| CN108640520A (en) * | 2018-05-28 | 2018-10-12 | 河北省沙河玻璃技术研究院 | Devitrified glass and reinforcing devitrified glass applied to 5G communication mobile terminal rear covers |
| CN108409147A (en) * | 2018-05-28 | 2018-08-17 | 河北省沙河玻璃技术研究院 | Devitrified glass and reinforcing devitrified glass applied to 5G communication mobile terminal protecgulums |
| CN108640520B (en) * | 2018-05-28 | 2021-08-10 | 河北省沙河玻璃技术研究院 | Microcrystalline glass and reinforced microcrystalline glass applied to rear cover of 5G communication mobile terminal |
| US11767258B2 (en) | 2018-11-16 | 2023-09-26 | Corning Incorporated | Glass compositions and methods for strengthening via steam treatment |
| US12234182B2 (en) | 2018-11-16 | 2025-02-25 | Corning Incorporated | Glass compositions and methods for strengthening via steam treatment |
| US11505492B2 (en) | 2019-05-16 | 2022-11-22 | Corning Incorporated | Glass compositions and methods with steam treatment haze resistance |
| US11370696B2 (en) | 2019-05-16 | 2022-06-28 | Corning Incorporated | Glass compositions and methods with steam treatment haze resistance |
| WO2020231963A1 (en) * | 2019-05-16 | 2020-11-19 | Corning Incorporated | Steam strengthenable glass compositions with low phosphorous content |
| US11767255B2 (en) | 2019-05-16 | 2023-09-26 | Corning Incorporated | Glass compositions and methods with steam treatment haze resistance |
| US12060298B2 (en) | 2019-05-16 | 2024-08-13 | Corning Incorporated | Glass compositions and methods with steam treatment haze resistance |
| US12122711B2 (en) | 2019-05-16 | 2024-10-22 | Corning Incorporated | Steam strengthenable glass compositions with low phosphorous content |
| US12404204B2 (en) | 2019-05-16 | 2025-09-02 | Corning Incorporated | Glasses with modified young's modulus profile |
| US11339084B2 (en) | 2020-05-12 | 2022-05-24 | Corning Incorporated | Fusion formable and steam strengthenable glass compositions with platinum compatibility |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2007031180A (en) | 2007-02-08 |
| JP5173123B2 (en) | 2013-03-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2007013538A1 (en) | Inorganic composition | |
| KR100590346B1 (en) | Low expansion glass-ceramics | |
| TWI361176B (en) | High strain point glasses | |
| JP3421284B2 (en) | Negatively heat-expandable glass ceramics and method for producing the same | |
| JP5416917B2 (en) | Glass | |
| KR102685757B1 (en) | Li2O-Al2O3-SiO2 crystallized glass | |
| JP5292028B2 (en) | Glass | |
| JP6978324B2 (en) | Ceramics and glass ceramics with low or negative thermal expansion | |
| JP2008297199A (en) | Low melting point lead-free solder glass and use thereof | |
| JP2011126728A (en) | Glass composition and glass substrate for flat panel display using the same | |
| CN102781864A (en) | Process for production of LAS-system crystalline glass | |
| JP4378152B2 (en) | Heat resistant glass | |
| CN115734949A (en) | White glass-ceramic substrate and article including tetragonal zirconia crystalline phase and method for manufacturing same | |
| JP2010116315A (en) | Crystallized glass | |
| WO2010029967A1 (en) | Glass | |
| KR102784753B1 (en) | High refractive index low density glass | |
| KR102784754B1 (en) | high refractive index glass | |
| WO2002096818A1 (en) | Crystallized glass for optical filter substrate and optical filter | |
| TWI298316B (en) | Aluminum silicophosphate glasses | |
| JP2010030848A (en) | Glass | |
| TWI232852B (en) | Composite solder glass with reduced melting temperature, filling material for same and methods of using same | |
| JP5292029B2 (en) | Glass | |
| JP2015166289A (en) | glass or crystallized glass | |
| CN108395096A (en) | Glass and float glass | |
| JP3087262B2 (en) | Crystallized glass |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| NENP | Non-entry into the national phase |
Ref country code: JP |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 06781736 Country of ref document: EP Kind code of ref document: A1 |