WO2011070703A1 - シリカ容器及びその製造方法 - Google Patents
シリカ容器及びその製造方法 Download PDFInfo
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- WO2011070703A1 WO2011070703A1 PCT/JP2010/006179 JP2010006179W WO2011070703A1 WO 2011070703 A1 WO2011070703 A1 WO 2011070703A1 JP 2010006179 W JP2010006179 W JP 2010006179W WO 2011070703 A1 WO2011070703 A1 WO 2011070703A1
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- silica
- inner layer
- substrate
- raw material
- forming
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D13/00—Containers having bodies formed by interconnecting two or more rigid, or substantially rigid, components made wholly or mainly of the same material, other than metal, plastics, wood, or substitutes therefor
- B65D13/02—Containers having bodies formed by interconnecting two or more rigid, or substantially rigid, components made wholly or mainly of the same material, other than metal, plastics, wood, or substitutes therefor of glass, pottery, or other ceramic material
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B19/00—Other methods of shaping glass
- C03B19/09—Other methods of shaping glass by fusing powdered glass in a shaping mould
- C03B19/095—Other methods of shaping glass by fusing powdered glass in a shaping mould by centrifuging, e.g. arc discharge in rotating mould
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B15/00—Single-crystal growth by pulling from a melt, e.g. Czochralski method
- C30B15/10—Crucibles or containers for supporting the melt
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B20/00—Processes specially adapted for the production of quartz or fused silica articles, not otherwise provided for
-
- 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
- C03C3/06—Glass compositions containing silica with more than 90% silica by weight, e.g. quartz
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/02—Elements
- C30B29/06—Silicon
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B35/00—Apparatus not otherwise provided for, specially adapted for the growth, production or after-treatment of single crystals or of a homogeneous polycrystalline material with defined structure
- C30B35/002—Crucibles or containers
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B2201/00—Type of glass produced
- C03B2201/06—Doped silica-based glasses
- C03B2201/30—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi
- C03B2201/54—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with beryllium, magnesium or alkaline earth metals
-
- 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
- C03C2201/00—Glass compositions
- C03C2201/06—Doped silica-based glasses
- C03C2201/30—Doped silica-based glasses containing metals
- C03C2201/54—Doped silica-based glasses containing metals containing beryllium, magnesium or alkaline earth metals
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- 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
Definitions
- the present invention relates to a silica container having silica as a main constituent and a method for producing the same, and more particularly to a low-cost, high dimensional accuracy, high heat-resistant silica container and a method for producing the same.
- Silica glass is a lens for projection exposure equipment (lithography equipment) for manufacturing large-scale integrated circuits (LSIs), prisms, photomasks and TFT substrates for displays, lamp tubes, window materials, reflectors, semiconductor industry cleaning containers, silicon Used as a semiconductor melting container.
- these silica glass raw materials must use expensive compounds such as silicon tetrachloride, and the silica glass melting temperature and processing temperature are about 2000 ° C., which is extremely high, resulting in high energy consumption and high cost. It was expensive. Therefore, conventionally, a method for producing silica glass using a relatively inexpensive powder raw material has been considered.
- Patent Document 1 at least two different silica glass particles, for example, silica glass fine powder and silica glass particles are mixed to form a water-containing suspension, then pressure-molded, and sintered at high temperature to contain silica.
- a method of obtaining a composite is shown.
- opaque silica is produced by preparing a mixed liquid (slurry) containing silica glass particles having a size of 100 ⁇ m or less and silica glass granules having a size of 100 ⁇ m or more, injecting the mixture into a mold, and then drying and sintering.
- a method of making a glass composite is shown.
- these conventional slip casting methods have a large shrinkage of the molded body in the drying process and the sintering process, and it has not been possible to produce a thick silica glass molded body with high dimensional accuracy.
- each of the methods for producing a silica glass molded body has problems. Therefore, even now, as a method for producing a silica crucible for producing single crystal silicon for LSI (for devices), the production methods described in Patent Document 3 and Patent Document 4 are used. In these methods, quartz powder or synthetic cristobalite powder treated with ultra-high purity is put into a rotating mold, and after molding, a carbon electrode is pushed in from the top and an electric discharge is applied to the carbon electrode to cause arc discharge. This is a method in which the quartz raw material powder is melted and sintered by raising the atmospheric temperature to the melting temperature range of quartz powder (estimated to be about 1800 to 2100 ° C.).
- Patent Document 5 discloses a method for improving the silicon melt etching resistance of a silica crucible for pulling a single crystal.
- Patent Document 5 shows the effect of applying a crystallization accelerator to the inner surface of a silica glass crucible.
- the crystallization accelerator alkaline earth metal elements Mg, Sr, Ca, Ba which are group 2a elements and Al of group 3b elements are shown.
- the silica glass crucible as shown in Patent Document 5 is not a bubble-free transparent silica glass layer having a complete inner surface portion of the crucible, but contains non-uniformly melted particles and minute bubbles of various dope elements. It was something to do.
- the pulled silicon single crystal often contains defects such as silica fine particles, voids, and pinholes as foreign matters. Further, there has been a problem that the fine bubbles existing inside the crucible are greatly expanded during the pulling of the silicon single crystal and the inner surface of the crucible is deformed.
- Patent Document 6 discloses a method of reducing bubbles in silica glass at the inner surface portion of a silica crucible for pulling up a single crystal and suppressing bubble expansion of the silica crucible in use.
- the silica crucible inner surface with less bubbles can be created by adding a hydrogen molecule concentration of 5 ⁇ 10 17 to 3 ⁇ 10 19 (molecules / cm 3 ) in the silica crucible raw material powder. ing.
- this method can reduce the bubble content on the inner surface of the silica crucible, the silicon melt etching resistance cannot be improved by crystallizing the inner surface of the silica crucible into cristobalite.
- hydrogen molecules doped in the raw material powder are gradually released to the outside during storage of the raw material powder, and there is a problem that the raw material powder containing hydrogen cannot be stored for a long time.
- Patent Document 7 discloses a method for reducing bubble growth when using a silica crucible for pulling silicon.
- a method of degassing from the outside while making the inside of the container molded body a hydrogen or helium gas atmosphere during arc discharge melting with a carbon electrode in crucible production is shown.
- this method can reduce the bubble content in the inner surface of the silica glass, but can reduce the OH group concentration contained in the silica crucible to a constant value, or when the silica crucible is used, the inner surface is finely cristobalite. The durability and heat resistance of the crucible could not be improved by crystallization.
- Patent Document 8 discloses a method for reducing the bubble content of a silica crucible for pulling up a silicon single crystal. In this, it is shown that hydrogen or / and helium gas is supplied to the powder compact of the container at the time of heating the crucible.
- helium gas or argon gas is supplied to the powder compact of the container at the time of heating in crucible manufacture, and then helium gas or argon gas is started and continued while arc melting is started and continued.
- the supply of hydrogen gas is stopped or the supply amount is reduced, and the supply of hydrogen gas is started.
- JP 2002-362932 A JP 2004-131380 A Japanese Patent Publication No.4-222861 Japanese Patent Publication No. 7-29871 JP-A-8-2932 JP 2007-326780 A JP-A-8-268727 Japanese Patent Laid-Open No. 9-20586 JP 2000-344536 A
- the present invention has been made in view of the problems as described above, and has a high dimensional accuracy and high heat resistance, and a silica container production method capable of producing a silica container mainly composed of silica at low cost, and An object is to provide such a silica container.
- the present invention has been made in order to solve the above-mentioned problems, and is formed on a substrate having rotational symmetry, silica as a main component, and containing bubbles at least in the outer peripheral portion, and the inner surface of the substrate.
- a method for producing a silica container comprising an inner layer made of transparent silica glass, wherein at least a raw material powder for forming the substrate has a particle size of 10 to 1000 ⁇ m and contains Li, Na, and K contained therein. The total concentration is 50 wt.
- the particle diameter is 10 to 1000 ⁇ m, and a total of at least one of Ca, Sr, and Ba is 50 to 2000 wt.
- a step of producing ppm-containing silica powder a step of charging the base material forming raw material powder into a mold, and temporarily forming the powder into a predetermined shape while rotating the mold to form a temporary molded body of the base; Introducing the inner layer forming raw material powder on the inner surface of the substrate temporary molded body, and forming the inner layer temporary molded body into a predetermined shape corresponding to the inner surface of the substrate temporary molded body, Hydrogen or helium or a mixed gas thereof at 10 vol.
- the outer peripheral portion of the base temporary molded body is a sintered body,
- a method for producing a silica container comprising a step of forming an inner peripheral portion of a temporary molded body of the base body and a temporary molded body of the inner layer as a molten glass body and forming the base body and the inner layer.
- the present invention also includes a substrate having rotational symmetry, having silica as a main component and containing bubbles in at least an outer peripheral portion, and an inner layer made of transparent silica glass formed on the inner surface of the substrate.
- a method for producing a silica container wherein at least a raw material powder for forming the substrate has a particle size of 10 to 1000 ⁇ m and a total concentration of Li, Na, and K contained is 50 wt.
- the particle diameter is 10 to 1000 ⁇ m, and a total of at least one of Ca, Sr, and Ba is 50 to 2000 wt.
- a step of producing ppm-containing silica powder a step of charging the base material forming raw material powder into a mold, and temporarily forming the powder into a predetermined shape while rotating the mold to form a temporary molded body of the base;
- the outer peripheral portion of the base temporary molded body is made a sintered body, and the inner peripheral portion of the base temporary molded body is a molten glass body.
- a step of forming the inner layer on the inner surface of the base body by heating at a high temperature from the inside by a discharge heating melting method in a gas atmosphere containing a ratio exceeding%.
- At least one of the steps by the discharge heating melting method can be performed while reducing the pressure from the outside of the substrate or the temporary molded body of the substrate through the mold.
- at least one of the steps by the discharge heating melting method can be performed while reducing the pressure from the outside of the substrate or the temporary molded body of the substrate through the mold. The dissolved gas in the manufactured silica container can be reduced more effectively.
- the inner layer forming raw material powder is made from 100 to 1000 wt. It is contained at a concentration of ppm, and Al is 10 to 100 wt. It is preferable to contain at a concentration of ppm. In this way, the inner layer forming raw material powder is made from 100 to 1000 wt. It is contained at a concentration of ppm, and Al is 10 to 100 wt. If it is contained at a concentration of ppm, the inner layer can be a silica glass layer having higher light transmittance and extremely few bubbles.
- the gas atmosphere containing hydrogen or helium or a mixed gas thereof is preferably set to a dew point temperature of 15 ° C. to ⁇ 15 ° C. and controlled within a range of ⁇ 2 ° C. of the set dew point temperature. If the dew point temperature of the gas atmosphere is set and controlled in this way, the OH group content and moisture (H 2 O) content in the silica container can be reduced to predetermined values while being low in cost. .
- the gas atmosphere containing hydrogen or helium or a mixed gas thereof has a content ratio of hydrogen or helium or a mixed gas thereof of 100 vol. % Is preferable.
- the content ratio of hydrogen, helium or a mixed gas thereof in the gas atmosphere is set to 100 vol. If it is set to%, generation
- the present invention has a rotational symmetry, has silica as a main component, contains bubbles in the outer peripheral portion, and includes a transparent silica glass in the inner peripheral portion, and is formed on the inner surface of the substrate.
- a silica container comprising an inner layer made of transparent silica glass, wherein the substrate has a total concentration of Li, Na, and K of 50 wt.
- the linear transmittance at a light wavelength of 600 nm of a 10 mm thick double-sided parallel optical polishing sample cut out from the transparent silica glass of the inner peripheral portion of the substrate is 91.8 to 93.2%, and the inner layer is , Li, Na, K total concentration is 100 wt.
- the 10 mm-thick double-sided parallel optical polishing sample cut from the inner layer has a linear transmittance of 91.8 to 93.2% at a light wavelength of 600 nm, and the sample cut from the inner layer is vacuum
- a silica container characterized in that the amount of water molecules released when heated to 1000 ° C. is less than 2 ⁇ 10 17 molecules / g.
- the container inner wall is provided with a high impurity diffusion preventing effect and durability, etc. when used at a high temperature. And generation of bubbles on the inner wall of the container can be effectively suppressed. As a result, it is possible to suppress the adverse effect of the bubbles generated on the inner wall of the silica container on the contents.
- the light transmittance value reflects the amount of bubbles in the glass and the uniform solubility of the doping element.
- the inner layer has Ba of 100 to 1000 wt. It is contained at a concentration of ppm, and Al is 10 to 100 wt. It is preferable to contain it at a concentration of ppm.
- the inner layer has a Ba content of 100 to 1000 wt. It is contained at a concentration of ppm, and Al is 10 to 100 wt. If it is contained at a concentration of ppm, the inner layer can be a silica glass layer having higher light transmittance and extremely few bubbles.
- the inner layer contains OH groups in an amount of 1 to 50 wt. ppm, each concentration of Li, Na, K is 20 wt. ppb or less, and each concentration of Ti, Cr, Mn, Fe, Ni, Cu, Zn, Zr, Mo, and W is 10 wt. It is preferably ppb or less. If the OH group concentration and the concentration of each metal contained in the inner layer are such concentrations, it is possible to more effectively reduce the contamination of impurities contained in the manufactured silica container.
- the method for producing a silica container according to the present invention a high impurity diffusion preventing effect and durability are obtained when the produced silica container is used at a high temperature, and the generation of bubbles on the inner wall of the silica container is effective. Can be suppressed.
- the silica container according to the present invention is a low-cost silica container having sufficient temperature uniformity, it has a high impurity diffusion preventing effect and durability on the inner wall of the container when used at a high temperature.
- the generation of bubbles on the inner wall of the container can be effectively suppressed. As a result, it is possible to suppress the adverse effect of the bubbles generated on the inner wall of the silica container on the contents.
- the production of the conventional silica container has problems in terms of dimensional accuracy and cost.
- a silica container manufactured by a conventional method for manufacturing a silica container for example, the incorporation of bubbles into a silicon single crystal in a silica crucible for growing a silicon single crystal, the discharge of bubbles into the contents There were problems such as adverse effects.
- the present inventors have studied in view of such problems, and have found the following problems.
- a silica container such as a crucible or boat for metal silicon melting and silicon single crystal or polycrystal production
- heat uniformity inside the container in a heated high temperature atmosphere is required.
- at least the silica container has a double structure, the outer side of the container is porous white opaque silica, and the inner side of the container is a thick colorless transparent silica glass substantially free of bubbles. .
- a second problem is to provide an action (impurity shielding action) for preventing diffusion of impurities. This is to suppress the adverse effect of contamination on the contents accommodated in the silica container due to the impurities contained in the silica container.
- impurity shielding action for preventing diffusion of impurities.
- impurity metal elements contained in a silica container at the time of production of silicon crystals such as alkali metal elements Li, Na, K, but particularly Ti, Cr, Mn, Fe, Ni, Cu, Zn, Zr, Mo, When W or the like is taken into the silicon crystal, the photoelectric conversion efficiency is lowered particularly in a silicon device for solar.
- the inner surface of the silica container is finely crystallized (glass ceramic) so that the impurities contained in the silica container do not diffuse into the silicon melt, thereby preventing the impurity from diffusing. Further, the quality of the fine crystallized portion on the inner surface of the silica container is such that each crystal size is fine and dense, so that the crystallized layer of fine cristobalite or the like is used.
- the third problem is to impart etching resistance by finely crystallizing the inner surface of the silica container with fine cristobalite or the like.
- the component (SiO 2 ) itself of the silica container is dissolved in the silicon melt, so that if oxygen element is taken into the silicon crystal, for example, in a silicon device for solar power, the photoelectric conversion efficiency is lowered. End up. Therefore, the inner surface of the silica container has the characteristic that it is difficult to dissolve in the silicon melt (having silicon melt etching resistance), that is, the inner surface of the container is similarly finely crystallized with fine cristobalite, etc.
- At least one of alkaline earth metal elements Ca, Sr, Ba as a crystallization accelerator is heterogeneously doped in the inner surface layer of the silica container, and the inner surface layer contains fine bubbles.
- the silicon crystal is produced, the contained gas is released from the bubbles, and these released gases are eluted into the silicon melt, so that the gas bubbles are taken into the silicon crystal and cause structural defects called pinholes and voids. . Therefore, it should be a thick silica glass layer that does not contain bubbles in the inner surface layer part of the silica container, is completely colorless and transparent as silica glass, and the alkali earth metal element is uniformly dissolved, and has high light transmittance. Is the fourth problem.
- the present invention solves the above four technical problems simultaneously at a lower cost than a silica container such as a conventional high-purity single crystal silicon pulling crucible using a high-purity silica raw material powder. It is necessary to solve this, and this is the fifth problem.
- silica container solar grade crucible
- metal silicon melting container used as a material for solar cells (solar power generation, solar power generation)
- the present invention is not limited to this, and can be widely applied to all silica containers used at high temperatures with silica as a main component.
- FIG. 4 shows a schematic cross-sectional view of an example of a silica container according to the present invention.
- the silica container 71 according to the present invention has rotational symmetry, and the basic structure thereof includes a base 51 and an inner layer 56.
- the substrate 51 has rotational symmetry and has silica as a main component.
- substrate 51 contains a bubble in the outer peripheral part 51a of a base
- the inner peripheral portion 51b of the base includes transparent silica glass.
- the inner layer 56 is formed on the inner surface of the base 51 and is made of transparent silica glass.
- the total concentration of Li, Na, and K in the substrate 51 is 50 wt. ppm or less.
- the inner layer 56 contains at least one of Ca, Sr, and Ba at a total concentration of 50 to 2000 wt.
- the linear transmittance of a 10 mm-thick double-sided parallel optical polishing sample at a light wavelength of 600 nm is 91.8 to 93.2%, more preferably 92.4 to 93.2%. It is.
- the amount of water molecules released when the sample cut out from the inner layer 56 is heated to 1000 ° C. under vacuum is less than 2 ⁇ 10 17 molecules / g, preferably less than 1 ⁇ 10 17 molecules / g.
- the linear transmittance at a light wavelength of 600 nm of the double-sided parallel optical polishing sample having a thickness of 10 mm cut out from the inner peripheral portion 51b of the substrate 51 is 91.8 to 93.2%.
- silica container of the present invention may further include other layers as long as it has at least the base 51 and the inner layer 56.
- the silica container 71 configured in this manner has sufficient temperature uniformity at low cost. That is, among the silica containers, at least the outer peripheral side 51a of the substrate is made of a porous opaque silica body, and at least the inner layer 56 is made of a thick transparent silica glass body substantially free of bubbles, thereby increasing the silica container 71. When used under temperature, the uniformity of the temperature inside the silica container 71 can be enhanced.
- the silica container 71 when used at a high temperature of 1400 to 1600 ° C. by containing at least one of Ca, Sr and Ba, particularly Ba, in the inner layer 56 as described above, the surface of the silica glass The portion can be recrystallized with cristobalite or the like. As a result, diffusion elution of alkali metal elements such as Na, K and Li contained in the base 51 of the silica container 71 can be prevented. It is possible to reduce the etching of the inner surface of the silica container 71 due to the containment such as the metal silicon melt processed in step (b). Ba is also preferable from the viewpoint that it is difficult to be taken into the produced silicon single crystal.
- the generation of bubbles in the inner layer 56 and the inner peripheral portion 51b of the base body can be effectively suppressed.
- double-sided parallel optics having a thickness of 10 mm cut out from the inner layer 56 as described above.
- the light transmittance of the polished sample at a light wavelength of 600 nm is 91.8 to 93.2%. Further, the light transmittance is 92.4 to 93.2% when there are few bubbles and the alkaline earth metal element is uniformly dissolved. Of these, 93.2% of the upper limit is the theoretical maximum value in silica glass.
- the silica container having a linear transmittance of 91.8 to 93.2% at a light wavelength of 600 nm of a double-sided parallel optical polishing sample having a thickness of 10 mm cut out from the inner peripheral portion 51b of the substrate 51 is also provided.
- 71 can be provided.
- the length other than one side of 10 mm is not particularly limited as long as the linear transmittance can be measured with the 10 mm-thick double-sided parallel optical polishing sample cut out from each of the above layers.
- a linear transmittance can be measured by preparing a sample of 2 mm ⁇ 2 mm ⁇ 10 mm.
- the inner layer 56 is made of 10-100 wt. By containing at a concentration of ppm, an impurity diffusion preventing effect can be further added and an alkaline earth metal element such as Ba can be more uniformly dissolved. Therefore, generation
- the raw material powder (silica powder) for forming the inner layer 56 is preliminarily made to contain elements that promote crystallization such as Ca, Sr, Ba, etc., and the atmosphere gas when the raw material powder is melt-treated is hydrogen.
- the atmosphere gas when the raw material powder is melt-treated is hydrogen.
- helium or a mixed gas thereof is 10 vol. % (Hereinafter, this atmosphere may simply be abbreviated as “hydrogen / helium-containing atmosphere”), so that the inner layer 56 does not contain fine bubbles. .
- a linear transmittance at a light wavelength of 600 nm in a 10 mm thick double-sided parallel optical polished finish sample is in the range of 91.8 to 93.2%, preferably in the range of 92.4 to 93.2%.
- the total value of at least one of Ca, Sr, and Ba is 50 to 2000 wt.
- ppm of silica powder is heated and melted in an atmosphere containing hydrogen / helium to form a transparent silica glass layer, preferably Ba is 100 to 1000 wt. ppm and Al is 10 to 100 wt.
- the formation of a transparent silica glass layer by heating and melting ppm silica powder in a hydrogen / helium-containing atmosphere has not been shown in the prior art, and is what the present inventors have thought and demonstrated for the first time.
- the total value of alkaline earth elements Ca, Sr, Ba is 50 wt. If it is less than ppm, a bubble-free inner layer is obtained, but recrystallization of the inner surface is difficult to occur when the silica container is used at a high temperature, and 2000 wt. If the value exceeds ppm, the concentration is too high, and it becomes difficult to uniformly dissolve these alkaline earth elements in the inner layer without bubbles. When the alkaline earth element is only Ba, the Ba concentration is 100 to 1000 wt.
- the mixing ratio of hydrogen or helium in the hydrogen / helium-containing atmosphere is 10 vol. %.
- an inert gas such as nitrogen or a rare gas, but the total value of hydrogen and helium is set to 100 vol. % Is more preferable.
- a crystallization accelerator such as Ba in the fused silica glass with a uniform concentration without containing bubbles.
- hydrogen molecules (H 2 ) react with oxygen molecules (O 2 ) having a large molecular radius to generate water (H 2 O) having a relatively small molecular radius, thereby producing silica glass. It is presumed that it is easily diffused and released to the outside and prevents the generation of bubbles.
- the water molecule content should be less than 2 ⁇ 10 17 (molecules / g) as the amount of water vapor released under vacuum at 1000 ° C.
- hydrogen molecules themselves have a small molecular radius and a high diffusion rate in silica glass, so even if they remain in silica glass, they do not cause bubbles.
- helium molecules ie, helium atoms
- Helium molecules have a smaller molecular radius than hydrogen molecules, and the gas molecules contained in silica glass It is presumed that it is easily diffused and released to the outside and prevents the generation of bubbles.
- Helium molecules have a smaller molecular radius than hydrogen molecules and a high diffusion rate in silica glass, so even if they remain in silica glass, they do not cause bubbles.
- silica fine crystals are generated in a large amount and uniformly on the surface of the silica glass. is important.
- hydrogen at 10 vol. In silica glass that has been heated and melted in an atmosphere containing more than%, the detailed mechanism is unknown, but the growth rate of crystals such as cristobalite tends to be slow. Accordingly, silica powder containing Ba or the like is supplied with hydrogen at 10 vol.
- a silica container is prepared by heat-melting treatment in an atmosphere containing more than%, a fine and dense recrystallized layer can be formed when the silica container is used.
- the linear transmittance at a light wavelength of 600 nm of the double-sided parallel optical polishing sample having a thickness of 10 mm cut out from the inner peripheral portion 51b of the base 51 is 91.8 to 93.2%.
- a silica container 71 can be provided.
- the inner peripheral portion 51b of the base 51 can also have a colorless and transparent silica glass layer substantially free of bubbles, for example, for a long time such as continuous pulling of silicon single crystal (multiple pulling). Even under conditions where the operation increases the amount of etching of the inner wall of the container and the amount of etching of the inner layer 56, it can withstand long-term use.
- the colorless and transparent silica glass layer substantially free of bubbles has a thickness of the substrate 51. It is preferable that it is about half (about 5 mm when the thickness of the base 51 is 10 mm).
- the inner layer 56 of the silica container 71 contains 1 to 50 wt. ppm, each concentration of Li, Na, K is 20 wt. ppb or less, and each concentration of Ti, Cr, Mn, Fe, Ni, Cu, Zn, Zr, Mo, and W is 10 wt. It is preferably ppb or less. This is because, when the OH group concentration and the concentration of each metal contained in the inner layer 56 are such concentrations, the contamination of impurities contained in the silica container 71 can be more effectively reduced. However, the OH group is 50 wt. Exceeding ppm is not preferable because the heat resistance of the silica container is lowered.
- silica container of the present invention which can produce the silica container 71 as described above, will be described more specifically.
- a method for producing a silica container (solar grade crucible) that can be manufactured at low cost and can be used as a container for melting and single crystal pulling of metal silicon (Si), which is used as a material for photovoltaic power generation devices, etc. explain.
- FIG. 1 shows an outline of an example (first embodiment) of a method for producing a silica container 71 according to the present invention.
- a substrate forming raw material powder 11 and an inner layer forming raw material powder 12 which are silica particles are prepared.
- the substrate forming raw material powder 11 is the main constituent material of the substrate 51 in the silica container 71 (see FIG. 4) according to the present invention.
- the substrate-forming raw material powder 11 can be produced, for example, by pulverizing and sizing the silica lump as follows, but is not limited thereto.
- a natural silica lump (naturally produced crystal, quartz, silica, siliceous rock, opal stone, etc.) with a diameter of about 5 to 50 mm is heated in a temperature range of 600 to 1000 ° C. for about 1 to 10 hours in an air atmosphere.
- the natural silica mass is put into water, taken out after rapid cooling, and dried. This process facilitates the subsequent crushing and sizing process using a crusher or the like, but the process may proceed to the crushing process without performing the heating and quenching process.
- the natural silica lump is pulverized and sized by a crusher or the like, and the particle size is adjusted to 10 to 1000 ⁇ m, preferably 50 to 500 ⁇ m to obtain natural silica powder.
- this natural silica powder is put into a rotary kiln composed of a silica glass tube having an inclination angle, and the inside of the kiln is made into an atmosphere containing hydrogen chloride (HCl) or chlorine (Cl 2 ) gas, and is kept at 700 to 1100 ° C.
- the high-purity treatment is performed by heating for about 1 to 100 hours. However, in a product application that does not require high purity, the process may proceed to the next process without performing the purification process.
- the substrate forming raw material powder 11 obtained after the above steps is crystalline silica.
- amorphous silica glass scrap may be used as the substrate forming raw material powder 11. it can.
- the particle diameter of the substrate forming raw material powder 11 is preferably 10 to 1000 ⁇ m, and more preferably 50 to 500 ⁇ m.
- the silica purity of the substrate forming raw material powder 11 is 99.99 wt. % Or more, preferably 99.999 wt. % Or more is more preferable.
- the total value of Li, Na, and K is 50 wt. ppm or less.
- the silica purity of the substrate forming raw material powder 11 is 99.999 wt. Even if it is a thing with comparatively low purity as% or less, the manufactured silica container can fully prevent the impurity contamination to the accommodation to accommodate. Therefore, a silica container can be manufactured at a lower cost than before.
- the substrate forming raw material powder 11 further contains Al, preferably 10 to 500 wt. It is good also as what is contained in the range of ppm.
- Al can be contained by, for example, adding nitrate, acetate, carbonate, chloride or the like as a water or alcohol solution, putting silica powder into these solutions, immersing them, and then drying them.
- the inner layer forming raw material powder 12 is a main constituent material of the inner layer 56 in the silica container 71 (see FIG. 4) according to the present invention.
- the inner layer forming raw material powder 12 has a particle size of 10 to 1000 ⁇ m, and a total of at least one of Ca, Sr and Ba is 50 to 2000 wt.
- a silica powder containing ppm is prepared. An outline of an example of a method for producing such an inner layer forming raw material powder 12 is shown in FIG.
- a powder made of silica having a particle size of 10 to 1000 ⁇ m is prepared as a raw material base material.
- the material of the raw material powder for forming the inner layer of the silica container include highly purified natural quartz powder, natural quartz powder, synthetic cristobalite powder, and synthetic silica glass powder. Crystalline silica powder is preferable for the purpose of reducing the amount of bubbles in the transparent layer, or synthetic powder is preferable for the purpose of obtaining a high-purity transparent layer.
- the particle size is preferably 100 to 500 ⁇ m. Purity is silica component (SiO 2 ) 99.9999 wt.
- % Or more and the total concentration of alkali metal elements Li, Na, and K is 100 wt. ppb or less, each 20 wt. ppb or less, preferably 10 wt. More preferably, it is ppb or less.
- Each of Ti, V, Cr, Fe, Co, Ni, Cu, Zn, Mo, and W is 10 wt. ppb or less, preferably 5 wt. More preferably, it is ppb or less.
- an alkaline earth metal element is added to the silica powder as the raw material base material.
- at least one of calcium (Ca) and strontium (Sr) barium (Ba), preferably Ba is contained in the silica powder.
- an alkaline earth metal element chloride, acetate, nitrate, carbonate or the like that dissolves in water or alcohol is selected, and an aqueous solution or alcohol solution of this compound is prepared.
- the powder to which the specific element is added is obtained by dipping and then drying.
- the inner layer forming raw material powder 12 can be manufactured.
- FIG. 5 is a cross-sectional view showing an outline of a mold that can be depressurized as an example of a mold for temporarily forming the substrate forming raw material powder 11.
- the depressurizable mold 101 is made of, for example, a member such as graphite and has rotational symmetry.
- a decompression hole 103 is distributed and formed in the inner wall 102 of the mold 101 that can be decompressed.
- the decompression hole 103 is continuous with the decompression passage 104.
- a pressure-reducing passage 105 also passes through a rotary shaft 106 for rotating the pressure-reducible mold 101, and vacuuming can be performed from here.
- a porous filter (not shown) is preferably attached to the hole 103.
- a mold 101 ′ as shown in FIG. 6 may be used instead of the depressurizable mold 101 shown in FIG. 5.
- the mold 101 ' is made of a member such as graphite and has rotational symmetry. It has a rotation shaft 106 ′ for rotating the mold 101 ′, and the inner wall 102 ′ has no particular hole.
- the substrate forming raw material powder 11 is introduced into the inner wall 102 of the depressurizable mold 101, and the base forming raw material powder 11 is temporarily formed into a predetermined shape corresponding to the shape of the inner wall 102 of the depressurizable mold 101. Let it be a temporary molded body 41 (see FIG. 7). Specifically, while rotating the depressurizable mold 101, the substrate forming raw material powder 11 is gradually put into the inner wall 102 of the depressurizable mold 101 from a raw material powder hopper (not shown), and centrifugal force is used. To form into a container shape.
- the thickness of the temporary molded body 41 of the base body may be adjusted to a predetermined amount by bringing a plate-shaped inner mold (not shown) from the inside into contact with the rotating powder.
- the method for supplying the substrate forming raw material powder 11 to the depressurizable mold 101 is not particularly limited.
- a hopper provided with a stirring screw and a measuring feeder can be used.
- the substrate forming raw material powder 11 filled in the hopper is stirred with a stirring screw and supplied while adjusting the supply amount with a measuring feeder.
- the inner layer forming raw material powder 12 is introduced onto the inner surface of the substrate temporary molded body 41, and the substrate temporary Temporarily molding into a predetermined shape corresponding to the inner surface of the molded body 41 is used as an inner layer temporary molded body 46.
- the method is the same as that in the case of introducing the substrate forming raw material powder 11 described above. That is, while rotating the depressurizable mold 101, the inner layer forming raw material powder 12 is gradually introduced from the raw material powder hopper into the inner surface of the temporary molded body 41 of the base and formed into a container shape using centrifugal force ( (See FIG. 8).
- the base 51 and the inner layer 56 are formed by a discharge heating melting method.
- the pressure is reduced by the pressure reducing hole 103 formed in the depressurizable mold 101, thereby forming the temporary molded body 41 of the base body.
- the inner layer temporary molded body 46 is degassed by depressurization from the outer peripheral side of the base temporary molded body 41 and heated from the inside of the base temporary molded body 41 and the inner layer temporary molded body 46 by a discharge heating melting method. To do.
- the outer peripheral portion of the substrate temporary molded body 41 is used as a sintered body, and the inner portion of the substrate temporary molded body 41 and the inner layer temporary molded body 46 are used as molten glass bodies to form the substrate 51 and the inner layer 56. .
- the temporary molding body 41 and the inner layer temporary molding are performed by the electric discharge heating melting method without performing any particular pressure reduction.
- the base body 51 and the inner layer 56 are formed by heating from the inside of the body 46 at a high temperature.
- an embodiment in which the base 51 and the inner layer 56 are formed while reducing the pressure using the pressure-reducible mold 101 will be mainly described. However, the same applies to the case where the pressure is not reduced and the pressure is reduced.
- substrate 51 and the inner layer 56 can be formed by the process of.
- the apparatus for forming the base 51 and the inner layer 56 includes a rotary motor (not shown), a discharge motor (not shown), and discharge heating melting (arc melting and arc discharge melting) in addition to the rotatable depressurizable mold 101 having rotational axis symmetry.
- a carbon electrode (carbon electrode) 212 serving as a heat source, an electric wire 212a, a high-voltage power supply unit 211, a lid 213, and the like.
- it includes components for adjusting the atmospheric gas supplied from the inside of the inner-layer temporary molded body 46, such as gas supply cylinders 411 and 412, a mixed gas supply pipe 420, a dehumidifier 430, a dew point thermometer 440, and the like. can do.
- hydrogen, helium, nitrogen or the like is supplied from the gas supply cylinders 411 and 412.
- a gas of 100% hydrogen when a gas of 100% hydrogen is used as the atmospheric gas, only one gas supply cylinder may be used.
- hydrogen or helium or a mixed gas thereof was added at 10 vol. It is also possible to prepare a gas (hydrogen / helium-containing atmosphere gas) contained in a ratio exceeding% in advance and supply this gas from a single gas cylinder.
- the dew point temperature is set to 15 ° C. to ⁇ 15 ° C. and the atmosphere is controlled in the range of ⁇ 2 ° C. of the set temperature. preferable. By doing in this way, it becomes possible to control the moisture content contained in the inner layer 56 and the OH group concentration combined with the silica glass network contained in the inner layer 56 to a constant value. Further, as the dew point temperature is lowered, OH groups can be reduced, and the concentration of OH groups is 1 to 50 wt. It is preferable to set it as ppm. However, the preferable dew point temperature can be determined depending on the use of the silica container.
- hydrogen is dehumidified to a predetermined dew point temperature or lower.
- helium or a mixed gas thereof is 10 vol.
- the atmosphere gas (hydrogen / helium-containing atmosphere gas) contained at a ratio exceeding% is started to be supplied from the inside of the base temporary molded body 41 and the inner layer temporary molded body 46. Specifically, as shown in FIG.
- hydrogen gas is supplied from a gas supply cylinder 411, and an inert gas other than hydrogen (for example, nitrogen (N 2 ), argon (Ar) is supplied from the gas supply cylinder 412. And helium (He)) are supplied and mixed, and supplied from the inside of the base temporary molded body 41 and the inner layer temporary molded body 46 through the mixed gas supply pipe 420.
- an inert gas other than hydrogen for example, nitrogen (N 2 ), argon (Ar) is supplied from the gas supply cylinder 412.
- helium (He) are supplied and mixed, and supplied from the inside of the base temporary molded body 41 and the inner layer temporary molded body 46 through the mixed gas supply pipe 420.
- symbol 510 shows the flow of mixed gas.
- the dew point temperature can be set by an appropriate dehumidifying device or the like, and an appropriate dew point thermometer or the like can be used to measure the dew point temperature.
- FIG. 9 shows a mode in which the dehumidifying device 430 and the dew point thermometer 440 are incorporated in the mixed gas supply pipe 420.
- the present invention is not limited to this, and the dew point temperature of the mixed gas can be set to a predetermined value range by dehumidification or the like. Good.
- the gas in the depressurizable mold 101 it is preferable to ventilate the gas in the depressurizable mold 101 as described above.
- This ventilation can be performed, for example, by letting the atmospheric gas in the depressurizable mold 101 escape from the gap of the lid 213 to the outside.
- symbol 520 shows the flow of atmospheric gas accompanying ventilation.
- the depressurizable mold 101 containing the base temporary molded body 41 and the inner layer temporary molded body 46 is rotated at a constant speed, and a degassing vacuum pump ( (Not shown) is activated, pressure is reduced from the outside of the temporary molded body 41 through the pressure reducing hole 103 and the pressure reducing passages 104 and 105, and charging is started between the carbon electrodes 212.
- a degassing vacuum pump (Not shown) is activated, pressure is reduced from the outside of the temporary molded body 41 through the pressure reducing hole 103 and the pressure reducing passages 104 and 105, and charging is started between the carbon electrodes 212.
- arc discharge (illustrated by reference numeral 220) is started between the carbon electrodes 212, the inner surface portions of the base temporary formed body 41 and the inner layer temporary formed body 46 are melted in a silica powder melting temperature range (about 1800 to 2000 ° C.). It is estimated) and melting starts from the outermost layer.
- the degree of vacuuming by the degassing vacuum pump increases (the pressure suddenly decreases), and the dissolved gas contained in the substrate forming raw material powder 11 and the inner layer forming raw material powder 12 is removed.
- the change to the fused silica glass layer proceeds from the inside to the outside while gassing.
- the timing of evacuation is important, and strong evacuation should not be performed before the inner surface layer inside the container is vitrified.
- the initial degree of decompression is not so high and the vacuuming is gradually strengthened as the inner surface is melted into glass.
- the inner layer and the inner half of the total thickness of the substrate are melted, the inner layer 56 is transparent silica glass, the inner peripheral side 51b of the substrate is a portion made of a transparent or translucent layer, and the outer peripheral portion of the substrate 51 (remaining) Heating by heating and depressurization by a vacuum pump are continued until 51a becomes sintered white opaque silica (opaque layer).
- the degree of vacuum is preferably 10 4 Pa or less, and more preferably 10 3 Pa or less. In this way, the silica container 71 of the present invention shown in FIG. 4 can be obtained.
- the inner layer forming step in the second embodiment as described later may be further performed once or a plurality of times so that the inner layer 56 is composed of a plurality of transparent silica glass layers having different purities and additives.
- FIG. 2 shows an outline of another example (second embodiment) of the method for producing the silica container 71 according to the present invention.
- the substrate forming raw material powder 11 and the inner layer forming raw material powder 12 which are silica particles are prepared. This step can be performed in the same manner as in the first embodiment described above.
- the base material forming powder 11 is introduced into a mold having rotational symmetry for molding.
- This step can also be performed in the same manner as in the first embodiment.
- the case where there is no need to perform discharge heating under reduced pressure is shown in FIG. A mold 101 ′ may be used.
- the substrate 51 is formed by a discharge heating melting method.
- the substrate temporary molded body 41 is replaced with the substrate temporary molded body 41 by reducing the pressure by the decompression hole 103 formed in the depressurizable mold 101. While depressurizing and degassing from the outer peripheral side, the substrate is heated from the inside of the temporary body of the base body by a discharge heating melting method. As a result, the outer peripheral portion of the base preform 41 is a sintered body, and the inner portion of the base preform 41 is a molten glass body to form the base 51.
- the substrate 51 is formed.
- substrate 51 is mainly demonstrated, reducing pressure using the mold 101 which can be pressure-reduced, However When not performing pressure reduction but performing at normal pressure, it is the same process except performing pressure reduction. Thus, the base 51 can be formed.
- the apparatus for forming the base 51 is a mold 101 that can be rotated and depressurized (or may be a mold 101 ′) having rotational axis symmetry.
- a rotation motor (not shown), and a carbon electrode (carbon electrode) 212 serving as a heat source for discharge heating melting (also referred to as arc melting or arc discharge melting), an electric wire 212a, a high-voltage power supply unit 211, a lid 213, and the like.
- the apparatus comprises components for adjusting the atmospheric gas supplied from the inside of the temporary molded body of the substrate, for example, gas supply cylinders 411 and 412, a mixed gas supply pipe 420, a dehumidifying device 430, a dew point thermometer 440, and the like. be able to.
- a hydrogen / helium-containing atmosphere that is set to a predetermined dew point temperature or less by dehumidification is used.
- the supply starts from the inside of the temporary molded body 41.
- hydrogen gas is supplied from a gas supply cylinder 411, and an inert gas other than hydrogen (for example, nitrogen (N 2 ), argon ( Ar) and helium (He)) are supplied and mixed, and supplied from the inside of the base preform 41 through the mixed gas supply pipe 420.
- symbol 510 shows the flow of mixed gas.
- the dew point temperature can be set by an appropriate dehumidifying device or the like, and an appropriate dew point thermometer or the like can be used to measure the dew point temperature.
- 10 and 11 show a mode in which the dehumidifying device 430 and the dew point thermometer 440 are incorporated in the mixed gas supply pipe 420, but the present invention is not limited to this, and the dew point temperature of the mixed gas is set to a predetermined value by dehumidification or the like. It only has to be in the range.
- the gas in the depressurizable mold 101 it is preferable to ventilate the gas in the depressurizable mold 101 as described above.
- This ventilation can be performed, for example, by letting the atmospheric gas in the depressurizable mold 101 escape from the gap of the lid 213 to the outside.
- symbol 520 shows the flow of atmospheric gas accompanying ventilation.
- the degassing vacuum pump (not shown) is started while rotating the depressurizable mold 101 containing the temporary molded body 41 of the base body at a constant speed. Then, the pressure is reduced from the outside of the temporary molded body 41 through the pressure reducing hole 103 and the pressure reducing passages 104 and 105, and charging is started between the carbon electrodes 212.
- the inner surface portion of the temporary body 41 of the base body becomes the melting temperature range of silica powder (estimated to be about 1800 to 2000 ° C.), and the outermost layer portion Melting begins from
- the degree of vacuuming by the degassing vacuum pump increases (the pressure suddenly decreases), and the fused silica glass layer degassed the dissolved gas contained in the substrate forming raw material powder 11.
- the timing of evacuation is important, and strong evacuation should not be performed before the inner surface layer inside the container is vitrified.
- the initial degree of decompression is not so high and the vacuuming is gradually strengthened as the inner surface is melted into glass. Then, the inner half of the entire thickness of the base body is melted, the inner peripheral side 51b of the base body becomes a portion made of a transparent or translucent layer, and the outer peripheral portion (the remaining outer half) 51a of the base body 51 is sintered white. Heating by applying electricity and depressurization by a vacuum pump are continued until opaque silica (opaque layer) is obtained.
- the degree of vacuum is preferably 10 4 Pa or less, and more preferably 10 3 Pa or less.
- the inner layer 56 is formed on the inner surface of the substrate 51 by heating at a high temperature from the inside.
- the inner layer 56 consist of several transparent silica glass layers from which purity and an additive differ by repeating this process.
- a method of forming the inner layer 56 will be described with reference to FIG.
- the apparatus for forming the inner layer 56 on the inner surface of the base 51 is the same as in the previous step, the rotatable depressurizable mold 101 on which the base 51 having rotational axis symmetry is installed, a rotary motor (not shown), And a raw material powder hopper 303 containing the inner layer forming raw material powder 12 for forming the inner layer 56, a stirring screw 304, a measuring feeder 305, a carbon electrode 212 serving as a heat source for discharge heating and melting, an electric wire 212a, a high voltage power supply unit 211, It consists of a lid 213 and the like.
- gas supply cylinders 411 and 412, a mixed gas supply pipe 420, a dehumidifier 430, a dew point thermometer 440, and the like may be further provided as in the previous step.
- the depressurizable mold 101 is set to a predetermined rotational speed, and a high voltage is gradually applied from the high-voltage power supply unit 211, and at the same time, the inner layer 56 is gradually formed from the raw material hopper 303.
- the inner layer forming raw material powder (high purity silica powder) 12 is sprayed from the upper part of the substrate 51.
- the discharge is started between the carbon electrodes 212, and the inside of the substrate 51 is in the silica powder melting temperature range (estimated to be about 1800 to 2000 ° C.), so that the dispersed inner layer forming raw material powder 12 is fused with silica.
- the particles adhere to the inner surface of the substrate 51.
- the carbon electrode 212, the raw material powder inlet, and the lid 213 installed in the upper opening of the base 51 have a mechanism that allows the position of the base 51 to be changed to some extent. By changing these positions, the base The inner layer 56 can be formed on the entire inner surface 51 with a uniform thickness.
- the step of forming the inner layer 56 by this discharge heating and melting method is preferably performed in an atmosphere set to a dew point temperature of 15 ° C. to ⁇ 15 ° C. and controlled within a range of ⁇ 2 ° C. of the set temperature.
- a dew point temperature 15 ° C. to ⁇ 15 ° C. and controlled within a range of ⁇ 2 ° C. of the set temperature.
- hydrogen gas is supplied from a gas supply cylinder 411, and an inert gas other than hydrogen (eg, nitrogen, argon, helium) is supplied from the gas supply cylinder 412 and mixed.
- the gas can be supplied from the inside of the base 51 through the mixed gas supply pipe 420.
- symbol 510 shows the flow of mixed gas.
- the gas in the depressurizable mold 101 can be ventilated. This ventilation can be performed, for example, by letting the atmospheric gas in the depressurizable mold 101 escape from the gap of the lid 213 to the outside.
- symbol 520 shows the flow of atmospheric gas accompanying ventilation.
- the silica container 71 according to the present invention shown in FIG. 4 can be manufactured.
- Example 1 In accordance with the method for producing a silica container of the present invention shown in FIG. 1 (first embodiment), a silica container was produced as follows.
- the purity of 99.999 wt. %, Natural quartz powder having a particle size of 50 to 500 ⁇ m was prepared.
- the raw material powder 12 for inner layer formation was prepared according to the procedure as shown in FIG. Specifically, first, a purity of 99.999 wt. %, And natural quartz powder having a particle diameter of 50 to 500 ⁇ m was prepared (FIG. 3 (1)).
- this natural quartz powder was immersed in an ethyl alcohol aqueous solution of barium nitrate having a predetermined concentration, and then heat-dried at 200 ° C. for 50 hours in a clean oven (FIG. 3 (2)).
- the raw material powder 12 for inner layer formation was obtained (FIG. 3 (3)).
- the substrate forming raw material powder 11 and the inner layer forming raw material powder 12 were integrally and temporarily formed as follows in a mold 101 as shown in FIG. First, while rotating a rotating cylindrical graphite depressurizable mold 101 having a decompression hole 103 formed in the inner wall 102, the substrate forming raw material powder 11 is introduced into the inner wall 102 of the mold to have a predetermined thickness. Then, the inner layer forming raw material powder 12 was added to form an inner layer temporary molded body 46 on the inner surface of the base temporary molded body 41 (see FIG. 8). Next, the atmosphere inside the temporary molded body 41 of the base and the temporary molded body 46 of the inner layer was changed to H 2 30 vol. %, He70 vol. % Of the mixed gas atmosphere.
- the dew point is 10 ° C. ⁇ 2 ° C., that is, in the range of 8 ° C. to 12 ° C., while gradually depressurizing and degassing the temporary molded body 41 of the base and the temporary molded body 46 of the inner layer with a vacuum pump from the outside of the mold 101.
- both temporary molded bodies were sintered and melted by the carbon electrode discharge heating melting method (arc discharge heating) (see FIG. 9).
- Example 2 In the same manner as in Example 1, except that the amount of Ba dope into the inner layer forming raw material powder 12 was approximately doubled, the silica container 71 was produced.
- Example 3 In the same manner as in Example 1, except that the amount of Ba dope into the inner layer forming raw material powder 12 was about four times the concentration, and Al was also doped at the same time, to produce a silica container 71.
- Example 4 As in Example 1, except that the amount of Ba dope into the inner layer forming raw material powder 12 was about 8 times the concentration and Al was also doped at the same time to produce a silica container 71.
- Example 5 As in Example 2, except that the atmosphere during heating under reduced pressure arc discharge of both temporary molded bodies was H 2 100 vol.
- the silica container 71 was manufactured as%.
- Example 6 As in Example 2, except that the atmosphere at the time of reduced-pressure arc discharge heating of both temporary molded bodies was H 2 50 vol. %, N 2 50 vol.
- the silica container 71 was manufactured as%.
- the silica container 71 was manufactured according to the method for manufacturing a silica container shown in FIG. 2 (second embodiment). First, the purity of 99.999 wt. %, Natural quartz powder having a particle size of 50 to 500 ⁇ m was prepared. Moreover, the raw material powder 12 for inner layer formation was prepared according to the procedure as shown in FIG. Specifically, first, a purity of 99.999 wt. %, And natural quartz powder having a particle diameter of 50 to 500 ⁇ m was prepared (FIG. 3 (1)). Next, this natural quartz powder was immersed in an ethyl alcohol aqueous solution of barium nitrate having a predetermined concentration, and then heat-dried at 200 ° C. for 50 hours in a clean oven (FIG. 3 (2)). Thus, the raw material powder 12 for inner layer formation was obtained (FIG. 3 (3)).
- the raw material powder 11 for substrate formation was temporarily formed in the mold 101 as shown in FIG. That is, while rotating a rotating cylindrical graphite depressurizable mold 101 having a decompression hole 103 formed in the inner wall 102, the substrate forming raw material powder 11 is introduced into the inner wall 102 of the mold to have a predetermined thickness. (See FIG. 7).
- the atmosphere inside the temporary molded body 41 of the base was changed to H 2 30 vol. %, He70 vol. % And the dew point temperature was controlled at 10 ° C. ⁇ 2 ° C.
- the base 51 was sintered and melted to form the base 51 by arc discharge heating under reduced pressure.
- the inner layer 56 was formed by arc discharge heating at normal pressure while spraying the inner layer forming raw material powder 12 from the upper part of the mold 101.
- the silica container 71 was manufactured.
- Example 8 As in Example 7, except that the atmosphere at the time of substrate formation was H 2 30 vol. %, N 2 70 vol.
- the silica container 71 was manufactured as%.
- Example 9 As in Example 2, except that the atmosphere during heating under reduced pressure arc discharge of both temporary molded bodies was H 2 15 vol. %, N 2 85 vol.
- the silica container 71 was manufactured as%.
- Example 10 As in Example 2, except that the atmosphere at the time of reduced-pressure arc discharge heating of both temporary molded bodies was He15 vol. %, N 2 85 vol.
- the silica container 71 was manufactured as%.
- a silica container (silica crucible) was produced in accordance with a conventional method.
- the raw material powder for forming the substrate and the raw material powder for forming the inner layer a particle diameter of 50 to 500 ⁇ m and a purity of 99.9999 wt. % High-purity quartz powder, particle size 50-300 ⁇ m, purity 99.9999 wt. % Cristobalite powder was prepared.
- the substrate is formed by atmospheric pressure arc heating in air that is not adjusted for humidity, and the inner layer is melted by atmospheric pressure arc heating in the same air while spraying raw material powder from the top of the mold. Formed.
- Comparative Example 3 As in Comparative Example 1, except that Ba is 3000 wt.
- the silica container was manufactured by performing high concentration dope with ppm.
- Comparative Example 4 Similar to Comparative Example 2, except that the raw material powder for substrate formation was purified to 99.99 wt. % Of the low-purity product, and the inner layer forming raw material powder was changed to high-purity synthetic cristobalite powder with Ba 100 wt. A silica container was produced using the ppm-doped material.
- Example 5 As in Example 2, except that the atmosphere at the time of reduced-pressure arc discharge heating of both the base and inner layer temporary molded bodies was H 2 5 vol. %, N 2 95 vol.
- the silica container 71 was manufactured as%.
- Example 6 (Comparative Example 6) As in Example 2, except that the atmosphere at the time of reduced-pressure arc discharge heating of both the base and inner layer temporary molded bodies was He5 vol. %, N 2 95 vol. The silica container 71 was manufactured as%.
- Particle size measurement method for each raw material powder Two-dimensional shape observation and area measurement of each raw material powder were performed with an optical microscope or an electron microscope. Next, assuming that the shape of the particle is a perfect circle, the diameter was calculated from the area value. This method was repeated statistically to obtain a value within the range of the particle size (in this range, 99 wt.% Or more of the raw material powder was included).
- Dew point temperature measurement Measured with a dew point thermometer. In addition, about each Example, it measured with the dew point thermometer 440 installed in the mixed gas supply pipe
- Impurity metal element concentration analysis When the impurity metal element concentration is relatively low (the glass is highly pure), plasma emission analysis (ICP-AES, Inductively Coupled Plasma-Atomic Emission Spectroscopy) or plasma mass spectrometry (ICP-MS, Inductively Coupled Pladded) When the impurity metal element concentration is relatively high (the glass is of low purity), atomic absorption spectrophotometry (AAS, Atomic Absorption Spectroscopy) was used.
- ICP-AES Inductively Coupled Plasma-Atomic Emission Spectroscopy
- ICP-MS Inductively Coupled Pladded
- Layer thickness measurement The thickness of the substrate and the inner layer was determined by measuring the cross section of the container at half the full height (200 mm height) of the side wall of the silica container.
- OH group concentration measurement Samples were cut and polished from the transparent portion of the substrate and the inner layer, and each was performed by infrared absorption spectrophotometry. Conversion to the OH group concentration follows the literature below. Dodd, D.D. M.M. and Fraser, D.A. B. (1966) “Optical determination of OH in fused silica.” Journal of Applied Physics, vol. 37, P.I. 3911.
- Water vapor gas emission measurement The amount of gas released from a granular silica glass sample adjusted to a particle size of 100 ⁇ m to 1 mm at 1000 ° C. under vacuum was measured with a mass spectrometer. Details follow the literature below. Water molecules H 2 O was expressed as the number of released molecules per unit weight (water molecules / g glass), assuming that all of the water molecules were released. Nasu, S .; et al. (1990) “Gas release of various kinds of vitreous silica”, Journal of Illuminating Engineering of Japan, vol. 74, no. 9, pp. 595-600.
- Light transmittance measurement A glass sample having dimensions of 5 mm ⁇ 5 mm ⁇ thickness of 11 mm was cut out from the inner layer, and both end faces were finished with a parallel optical polishing of 10 mm thickness (surface accuracy 1 / 20 ⁇ , wavelength 633 nm). After that, the visible light transmittance meter using a mercury lamp as a light source is used to measure the linear transmittance of the glass sample at 600 nm (the incident light is 100%, the reflection of the sample surface, the back reflection inside the sample, and the absorption of the sample itself). This is a value obtained by subtracting, and is called Optical transmission). The theoretical transmittance is a maximum of 93.2%. Since incident light is scattered by fine bubbles, fine particles, clusters, etc. in the glass sample, the value of light transmittance is determined by the fact that various dissolved elements are dissolved in the silica glass without bubbles and uniformly. It is effective for.
- Silicon single crystal continuous pulling (multi pulling) evaluation In the produced silica container, the purity was 99.9999999 wt. % Metal polysilicon was added, the temperature was raised to obtain a silicon melt, and then the silicon single crystal was pulled three times repeatedly (multi-pulling), and the success rate of single crystal growth was evaluated.
- the pulling conditions were as follows: the inside of the CZ apparatus was an argon (Ar) gas 100% atmosphere at a pressure of 10 3 Pa, the pulling rate was 1 mm / min, the rotation speed was 10 rpm, the silicon single crystal dimensions were 150 mm in diameter and 150 mm in length. The operation time for one batch was about 12 hours.
- the evaluation classification of the success rate of three times of single crystal growth was as follows. Successful 3 times ⁇ (Good) Successful ⁇ (Slightly bad) 1 time or less x (defect)
- etching resistance of silica containers From the silica container side wall of the lower part of the silica container after the multi-pulling of the silicon single crystal three times, the inner wall surface had all the thicknesses in the thickness direction so that the dimension of the inner wall surface was 100 mm ⁇ 100 mm. The sample was cut out as it was. Next, the etching amount of the inner wall portion of the inner layer was determined by measuring the sample cross section with a scale. The etched thickness of the inner layer is less than 3 mm ⁇ (good) The etched thickness of the inner layer is 3 mm to less than 5 mm. Etched thickness of inner layer is 5mm or more x (defect)
- Manufacturing cost (relative) evaluation of silica container The production cost of the silica container was evaluated. In particular, the total values of silica raw material costs, melting energy costs, etc. were relatively evaluated. Conventional production costs were based on Comparative Example 2. Low cost ⁇ (Less than 50% of conventional manufacturing cost) Medium cost ⁇ (50 to less than 100% of conventional manufacturing cost) Cost is high ⁇ (Conventional manufacturing cost is 100%)
- Tables 1 to 8 below summarize the production conditions, measured physical property values, and evaluation results of the silica containers produced in Examples 1 to 10 and Comparative Examples 1 to 6.
- the present invention is not limited to the above embodiment.
- the above embodiment is merely an example, and the present invention has the same configuration as that of the technical idea described in the claims of the present invention, and any device that exhibits the same function and effect is the present invention. It is included in the technical scope of the invention.
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Abstract
Description
このように、本発明のシリカ容器の製造方法では、放電加熱溶融法による工程のうち少なくとも一つを、型枠を通じて基体又は基体の仮成形体の外側から減圧しながら行うことができ、その場合、製造されるシリカ容器中の溶存ガスをより効果的に低減することができる。
このように、内層形成用原料粉を、Baを100~1000wt.ppmの濃度で含有し、Alを10~100wt.ppmの濃度で含有するものとすれば、内層を、より光透過率が高く、気泡が極めて少ないシリカガラス層とすることができる。
このように上記ガス雰囲気の露点温度を設定、制御すれば、低コストでありながらも、シリカ容器中のOH基含有量、水分(H2O)含有量を所定の値に低減することができる。
このように上記ガス雰囲気における水素若しくはヘリウム又はそれらの混合ガスの含有比率を100vol.%とすれば、より効果的にシリカ容器の内壁部での気泡の発生を抑制することができる。
このように、内層が、Baを100~1000wt.ppmの濃度で含有し、Alを10~100wt.ppmの濃度で含有するものであれば、内層を、より光透過率が高く、気泡が極めて少ないシリカガラス層とすることができる。
内層に含まれるOH基濃度、各金属の濃度がこのような濃度であれば、製造したシリカ容器に収容する収容物への不純物汚染をより効果的に低減することができる。
また、本発明に従うシリカ容器であれば、低コストで、十分な温度均一性を有するシリカ容器でありながらも、高温度下での使用に際して、容器内壁に高い不純物拡散防止効果及び耐久性等を持たせることができるとともに、容器内壁における気泡の発生が効果的に抑制されたものとすることができる。その結果、シリカ容器内壁に発生した気泡の、収容物への悪影響を抑制することができる。
また、これに加えて、例えばシリコン単結晶成長用シリカルツボにおけるシリコン単結晶への気泡の取り込みのように、従来のシリカ容器の製造方法により製造されたシリカ容器では、収容物への気泡の放出による悪影響等の問題があった。
まず、金属シリコン溶融及びシリコン単結晶又は多結晶製造用のルツボやボート等のシリカ容器では、加熱高温雰囲気での容器内部の均熱性が必要とされる。そのためには少なくともシリカ容器を2重構造とし、容器外側は多孔質の白色不透明シリカとし、容器内側は実質的に気泡を含まない肉厚の無色透明シリカガラスとすることが第1の課題である。
例えば、シリコン結晶の製造時にシリカ容器に含まれている不純物金属元素、例えばアルカリ金属元素Li、Na、Kのみならず、特にTi、Cr、Mn、Fe、Ni、Cu、Zn、Zr、Mo、W等がシリコン結晶に取り込まれた場合、特にソーラー用シリコンデバイスにおいて光電変換効率の低下を引き起こしてしまう。従って、シリカ容器に含まれる不純物がシリコン融液に拡散してこないようにシリカ容器の内表面を微細結晶化(グラスセラミック化)させて、不純物の拡散を防止する作用を持たせる。また、このシリカ容器の内表面の微細結晶化部分の品質としても、各々の結晶寸法が微細、緻密であるため、きめの細かいクリストバライト等の結晶化層とするものである。
例えば、シリコン単結晶の製造時に、シリカ容器の成分(SiO2)そのものがシリコン融液に溶解し、そのため酸素元素がシリコン結晶に取り込まれると例えばソーラー用シリコンデバイスにおいて光電変換効率の低下を引き起こしてしまう。従って、シリカ容器の内表面がシリコン融液に対して溶解しにくい(耐シリコン融液エッチング性のある)特性を有するもの、すなわち同様に容器の内表面をきめの細かなクリストバライト等により微細結晶化させたものとする。
本発明に係るシリカ容器71は回転対称性を有し、その基本構造は、基体51と、内層56とから成る。
この基体51は、回転対称性を有し、シリカを主成分とする。また、基体51は、基体の外周部分51aに、気泡を含有する。すなわち、基体の外周部分が多孔質で白色不透明層部を有する。また、基体の内周部分51bに透明シリカガラスを含む。
また、内層56は、基体51の内表面上に形成され、透明シリカガラスからなる。
また、内層56が、Ca、Sr、Baの少なくとも1種を合計濃度50~2000wt.ppmで含有するものであり、かつ、厚さ10mmの両面平行光学研磨試料の光波長600nmにおける直線透過率が91.8~93.2%であり、より好ましくは92.4~93.2%である。さらに、内層56から切り出した試料を真空下にて1000℃に加熱したときの水分子の放出量が2×1017分子/g未満であり、好ましくは1×1017分子/g未満である。
さらに、本発明に係るシリカ容器では、基体51においても内周部分51bから切り出した厚さ10mmの両面平行光学研磨試料の光波長600nmにおける直線透過率が91.8~93.2%である。
このようなAl原子のSi原子との置換は、電荷バランスを取るためにBa2+等のアルカリ土類金属元素の陽イオンも固定する作用があると考えられ、Ba等の元素をより均一に溶解させることができ、この点からもシリカガラス中の気泡を抑制することができる。
ヘリウム分子は、水素分子よりもさらに分子半径が小さく、シリカガラス中の拡散速度も速いので、シリカガラス中に残留していても、気泡生成の原因とならない。
まず、図1の(1)に示したように、シリカ粒子である基体形成用原料粉11及び内層形成用原料粉12を準備する。
この基体形成用原料粉11は例えば以下のようにしてシリカ塊を粉砕、整粒することにより作製することができるが、これに限定されない。
次いで、この天然シリカ粉を、傾斜角度を有するシリカガラス製チューブから成るロータリーキルンの中に投入し、キルン内部を塩化水素(HCl)又は、塩素(Cl2)ガス含有雰囲気とし、700~1100℃にて1~100時間程度加熱することにより高純度化処理を行う。ただし高純度を必要としない製品用途では、この高純度化処理を行わずに次処理へ進んでもよい。
基体形成用原料粉11の粒径は、上記のように、10~1000μmとすることが好ましく、50~500μmとすることがより好ましい。
基体形成用原料粉11のシリカ純度は、99.99wt.%以上とすることが好ましく、99.999wt.%以上とすることがさらに好ましい。特に、Li、Na、Kの合計値は、50wt.ppm以下とする。また、本発明のシリカ容器の製造方法であれば、基体形成用原料粉11のシリカ純度を99.999wt.%以下と比較的低純度のものとしても、製造されるシリカ容器は、収容する収容物への不純物汚染を十分に防止することができる。そのため、従来よりも低コストでシリカ容器を製造することができることになる。
Alは、例えば硝酸塩、酢酸塩、炭酸塩、塩化物等を水又はアルコール溶液として、これら溶液の中にシリカ粉を投入、浸漬させ、次いで乾燥することにより含有させることができる。
このような内層形成用原料粉12の製造方法の一例の概略を、図3に示す。
シリカ容器の内層形成用原料粉の材質としては、高純度化処理された天然石英粉、天然水晶粉、又は合成クリストバライト粉、合成シリカガラス粉が挙げられる。透明層の気泡量を少なくする目的であれば結晶質シリカ粉が好ましく、あるいは高純度な透明層とする目的であれば、合成粉が好ましい。粒径は好ましくは100~500μmである。純度はシリカ成分(SiO2)99.9999wt.%以上、かつアルカリ金属元素Li、Na、Kの合計濃度が100wt.ppb以下であり、各々を20wt.ppb以下とすることが好ましく、各々を10wt.ppb以下とすることがより好ましい。また、Ti、V、Cr、Fe、Co、Ni、Cu、Zn、Mo、Wの各々が10wt.ppb以下とすることが好ましく、各々を5wt.ppb以下とすることがさらに好ましい。
具体的には、カルシウム(Ca)、ストロンチウム(Sr)バリウム(Ba)の少なくとも1種以上、好ましくはBaをシリカ粉末に含有させる。含有のさせ方としては、水又はアルコールに溶解するアルカリ土類金属元素の塩化物、酢酸塩、硝酸塩又は炭酸塩等を選び、この化合物の水溶液またはアルコール溶液を作成しこの中にシリカ原料粉を浸漬させ、その後乾燥させることにより特定元素が添加された粉末が得られる。
図5に、基体形成用原料粉11を仮成形する型枠の一例として、減圧可能な型枠の概略を表す断面図を示した。減圧可能な型枠101は、例えば、グラファイト等の部材から成り、回転対称性を有している。また、減圧可能な型枠101の内壁102には、減圧用の孔103が分配されて形成されている。減圧用の孔103は、減圧用の通路104に連なっている。また、減圧可能型枠101を回転させるための回転軸106にも減圧用の通路105が通っており、ここから真空引きを行うことができるようになっている。なお、孔103には多孔質のフィルター(図示せず)を取り付けることが好ましい。
具体的には、減圧可能型枠101を回転させつつ、原料粉ホッパー(図示せず)から徐々に基体形成用原料粉11を減圧可能型枠101の内壁102に投入し、遠心力を利用して容器形状に成形する。また内側から板状の内型枠(図示せず)を、回転する粉体に接触させることにより、基体の仮成形体41の肉厚を所定量に調整してもよい。
また、この基体形成用原料粉11の減圧可能型枠101への供給方法は特に限定されないが、例えば、攪拌用スクリューと計量フィーダを備えるホッパーを用いることができる。この場合、ホッパーに充填された基体形成用原料粉11を、攪拌用スクリューで攪拌し、計量フィーダで供給量を調節しながら供給する。
基本的には上記の基体形成用原料粉11の導入の場合と同様の手法である。すなわち、減圧可能型枠101を回転させつつ、原料粉ホッパーから徐々に内層形成用原料粉12を基体の仮成形体41の内表面に投入し、遠心力を利用して容器形状に成形する(図8参照)。
減圧しながら加熱溶融を行う場合には、具体的には、図9に示すように、減圧可能型枠101に形成されている減圧用の孔103によって減圧することにより、基体の仮成形体41及び内層の仮成形体46を、基体の仮成形体41の外周側から減圧して脱ガスするとともに、放電加熱溶融法により、基体の仮成形体41及び内層の仮成形体46の内側から加熱する。これによって、基体の仮成形体41の外周部分を焼結体とするとともに、基体の仮成形体41の内側部分及び内層の仮成形体46を溶融ガラス体とし、基体51と内層56を形成する。
以下では、減圧可能型枠101を用いて減圧しながら基体51及び内層56の形成を行う態様を主に説明するが、減圧を行わず、常圧で行う場合も、減圧を行うこと以外は同様の工程によって基体51及び内層56を形成することができる。
このようにして、図4に示した本発明のシリカ容器71とすることができる。
この工程は上述した第1の実施態様の場合と同様に行うことができる。
この工程についても第1の実施態様の場合と同様に行うことができる。また、第1の実施態様の場合と同様に、図5、図7に示した減圧可能型枠101の他、減圧下にて放電加熱をする必要がない場合などには、図6に示した型枠101’を用いても良い。
以下では、減圧可能な型枠101を用いて減圧しながら基体51の形成を行う態様を主に説明するが、減圧を行わず、常圧で行う場合も、減圧を行うこと以外は同様の工程によって基体51を形成することができる。
そして、基体の全厚さの内側半分程度が溶融し、基体の内周側51bが透明ないし半透明の層からなる部分となり、基体51の外周部分(残り外側半分程度)51aが焼結した白色不透明シリカ(不透明層)となるまで加電による加熱と真空ポンプによる減圧を継続する。減圧度は104Pa以下とすることが好ましく、103Pa以下とすることがさらに好ましい。
なお、この工程を繰り返すことにより、内層56を純度や添加物が異なる複数の透明シリカガラス層からなるようにしてもよい。
基体51の内表面上への内層56を形成する装置は前工程と同様、回転軸対称性を有する基体51が設置されている回転可能な減圧可能型枠101、回転モーター(図示せず)、及び内層56形成のための内層形成用原料粉12が入った原料粉ホッパー303、攪拌用スクリュー304、計量フィーダ305、及び放電加熱溶融の熱源となる炭素電極212、電線212a、高圧電源ユニット211、蓋213等から成る。また、雰囲気ガスを調整する場合には、前工程と同様に、さらに、ガス供給用ボンベ411、412、混合ガス供給管420、除湿装置430、露点温度計440等を具備していてもよい。
(実施例1)
図1に示した本発明のシリカ容器の製造方法(第1の実施態様)に従い、以下のように、シリカ容器を製造した。
また、内層形成用原料粉12を図3に示したような手順に従って準備した。具体的には、まず、純度99.999wt.%、粒径50~500μmの天然石英粉を準備した(図3(1))。次に、この天然石英粉を、所定濃度の硝酸バリウムのエチルアルコール水溶液に浸漬させ、その後クリーンオーブンの中で200℃、50時間の加熱乾燥処理を行った(図3(2))。このようにして、内層形成用原料粉12を得た(図3(3))。
次に、基体の仮成形体41及び内層の仮成形体46の内側の雰囲気を、H230vol.%、He70vol.%の混合ガス雰囲気へ置換した。型枠101の外側から真空ポンプにて基体の仮成形体41及び内層の仮成形体46を徐徐に減圧、脱ガスさせつつ、露点10℃±2℃、すなわち、8℃から12℃の範囲に制御して、カーボン電極放電加熱溶融法(アーク放電加熱)により両仮成形体の焼結、溶融を行った(図9参照)。
実施例1と同様に、ただし、内層形成用原料粉12へのBaドープ量を約2倍の濃度として、シリカ容器71を製造した。
実施例1と同様に、ただし、内層形成用原料粉12へのBaドープ量を約4倍の濃度として、またAlも同時にドープして、シリカ容器71を製造した。
実施例1と同様に、ただし、内層形成用原料粉12へのBaドープ量を約8倍の濃度として、またAlも同時にドープして、シリカ容器71を製造した。
実施例2と同様に、ただし、両仮成型体の減圧アーク放電加熱時の雰囲気をH2100vol.%として、シリカ容器71を製造した。
実施例2と同様に、ただし、両仮成型体の減圧アーク放電加熱時の雰囲気をH250vol.%、N250vol.%として、シリカ容器71を製造した。
図2に示したシリカ容器の製造方法(第2の実施態様)に従ってシリカ容器71の製造を行った。
まず、基体形成用原料粉11として、純度99.999wt.%、粒径50~500μmの天然石英粉を準備した。
また、内層形成用原料粉12を図3に示したような手順に従って準備した。具体的には、まず、純度99.999wt.%、粒径50~500μmの天然石英粉を準備した(図3(1))。次に、この天然石英粉を、所定濃度の硝酸バリウムのエチルアルコール水溶液に浸漬させ、その後クリーンオーブンの中で200℃、50時間の加熱乾燥処理を行った(図3(2))。このようにして、内層形成用原料粉12を得た(図3(3))。
このようにして、シリカ容器71を製造した。
実施例7と同様に、ただし、基体形成時の雰囲気をH230vol.%、N270vol.%として、シリカ容器71の製造を行った。
実施例2と同様に、ただし、両仮成型体の減圧アーク放電加熱時の雰囲気をH215vol.%、N285vol.%として、シリカ容器71を製造した。
実施例2と同様に、ただし、両仮成型体の減圧アーク放電加熱時の雰囲気をHe15vol.%、N285vol.%として、シリカ容器71を製造した。
基体形成用原料粉、内層形成用原料粉として、それぞれ、粒径50~500μm、純度99.999wt.%の高純度石英粉、粒径50~300μm、純度99.9999wt.%のクリストバライト粉を準備した。基体及び内層の仮成形体を特には湿度調整を行っていない空気中にて形成、減圧アーク放電加熱して溶融し形成した。
以下のように、概ね従来法に従ってシリカ容器(シリカルツボ)を作製した。
基体形成用原料粉、内層形成用原料粉として、それぞれ、粒径50~500μm、純度99.9999wt.%の高純度石英粉、粒径50~300μm、純度99.9999wt.%のクリストバライト粉を準備した。基体は特には湿度調整を行っていない空気中にて常圧アーク放電加熱して形成し、内層は同様の空気中にて原料粉を型枠上部から散布しつつ常圧アーク放電加熱して溶融し形成した。
比較例1と同様に、ただし、内層形成用原料粉にBaを3000wt.ppmと高濃度ドープを行って、シリカ容器の製造を行った。
比較例2と同様に、ただし、基体形成用原料粉を純度99.99wt.%の低純度品とし、内層形成用原料粉を高純度合成クリストバライト粉にBa100wt.ppmドープしたものを用いてシリカ容器の製造を行った。
実施例2と同様に、ただし、基体及び内層の両仮成型体の減圧アーク放電加熱時の雰囲気をH25vol.%、N295vol.%として、シリカ容器71を製造した。
実施例2と同様に、ただし、基体及び内層の両仮成型体の減圧アーク放電加熱時の雰囲気をHe5vol.%、N295vol.%として、シリカ容器71を製造した。
各実施例及び比較例において用いた原料粉及び雰囲気ガス、並びに製造したシリカ容器の物性、特性評価を以下のようにして行った。
光学顕微鏡又は電子顕微鏡で各原料粉の二次元的形状観察及び面積測定を行った。次いで、粒子の形状を真円と仮定し、その面積値から直径を計算して求めた。この手法を統計的に繰り返し行い、粒径の範囲の値とした(この範囲の中に99wt.%以上の原料粉が含まれる)。
露点温度計によって測定した。
なお、各実施例については、上記のように、混合ガス供給管420に設置した露点温度計440により測定を行った。
不純物金属元素濃度が比較的低い(ガラスが高純度である)場合は、プラズマ発光分析法(ICP-AES、Inductively Coupled Plasma - Atomic Emission Spectroscopy)又はプラズマ質量分析法(ICP-MS、Inductively Coupled Plasma - Mass Spectroscopy)で行い、不純物金属元素濃度が比較的高い(ガラスが低純度である)場合は、原子吸光光度法(AAS、Atomic Absorption Spectroscopy)で行った。
シリカ容器の側壁の全高さの半分部分(高さ200mmの部分)における容器断面をスケールで測定することにより、基体及び内側層の厚さを決めた。
基体及び内層の透明部分からサンプルを切断、研磨し、それぞれについて赤外線吸収分光光度法で行った。OH基濃度への換算は、以下文献に従う。
Dodd,D.M. and Fraser,D.B.(1966) “Optical determination of OH in fused silica.” Journal of Applied Physics, vol.37, P.3911.
粒径100μm~1mmに調整した粒状シリカガラスサンプルからの、真空下1000℃におけるガス放出量を質量分析装置により測定した。詳細は下記文献に従う。水分子H2Oは全量放出したものとして、単位重量当りの放出分子数(水分子/ガラスg)として表現した。
Nasu,S.et al.(1990) “Gas release of various kinds of vitreous silica”, Journal of Illuminating Engineering Institute of Japan, vol.74, No.9, pp.595-600.
内層から、寸法5mm×5mm×厚さ11mm程度のガラスサンプルを切り出し、両端面を厚さ10mm平行光学研磨仕上げ(面精度1/20λ、波長633nm)した。その後、水銀ランプを光源とする可視光透過率計により、該ガラスサンプルの600nmでの直線透過率(入射光を100%として、サンプルの表面の反射とサンプル内部の裏面反射及びサンプル自体の吸収を差し引いた値であり、Optical transmission と呼ばれる)を測定した。理論透過率は最大93.2%である。
入射光は、ガラスサンプル中の微細気泡や微粒子、クラスター等により散乱されるため、光透過率の値は、シリカガラス中に各種の溶存元素が無気泡でかつ均一に溶解されていることの判定に有効である。
製造したシリカ容器の中に純度99.9999999wt.%の金属ポリシリコンを投入し、昇温を行いシリコン融液とし、次いでシリコン単結晶の引上げを3回繰り返して行い(マルチ引上げ)、単結晶育成の成功率として評価した。引上げ条件は、CZ装置内を103Paの圧力のアルゴン(Ar)ガス100%雰囲気で、引上げ速度1mm/分、回転数10rpm、シリコン単結晶寸法を直径150mm、長さ150mmとした。また、1バッチの操業時間は約12時間とした。単結晶育成3回繰り返しの成功率の評価分類は以下の通りとした。
3回成功 ○(良好)
2回成功 △(やや不良)
1回以下 ×(不良)
前記のシリコン単結晶マルチ引上げにおいて、各シリコン単結晶マルチ引上げ後の2本目のシリコン単結晶の任意の部位から、直径150mm、厚さ200μmの両面研磨仕上げのシリコンウエーハ各10枚を作製した。次いで各々のシリコンウエーハの両面に存在するボイドとピンホールの個数を測定し、統計的に数値処理を行い単位面積(m2)当りの平均ボイド及びピンホール数を求めた。
平均ボイド及びピンホール数が1個/m2未満 ○(良好)
平均ボイド及びピンホール数が1~2個/m2 △(やや不良)
平均ボイド及びピンホール数が3個/m2以上 ×(不良)
シリコン単結晶3回マルチ引上げ後のシリカ容器の、当初のシリコン溶融面より下位部分のシリカ容器側壁から、内壁面の寸法が100mm×100mmとなるように、厚さ方向の全ての厚みを有したままサンプルを切り出した。次いで、内層の内壁部のエッチング量を、サンプル断面をスケールで測定することにより求めた。
内層のエッチングされた厚さが3mm未満 ○(良好)
内層のエッチングされた厚さが3mm~5mm未満 △(やや不良)
内層のエッチングされた厚さが5mm以上 ×(不良)
シリコン単結晶3回マルチ引上げ後のシリカ容器の、当初のシリコン溶融面より下位部分のシリカ容器側壁から、内壁面の寸法が100mm×100mmとなるように、厚さ方向の全ての厚みを有したままサンプルを切り出した。次いで、内層内の気泡を、実体顕微鏡で観察することにより、気泡の膨張性の相対的評価を行った。従来レベルは比較例2を基準とした。
気泡の膨張がほとんど認められない ○(良好)
気泡の膨張が少し認められる △(やや不良)
気泡の膨張が従来レベルで認められる ×(不良)
シリカ容器の製造コストを評価した。特に、シリカ原料費、溶融エネルギー費等の合計値を相対的に評価した。従来製法コストは比較例2を基準とした。
コストが低い ○(従来製法コストの50%未満)
コストが中程度 △(従来製法コストの50~100%未満)
コストが大きい ×(従来製法コストを100%とする)
Claims (9)
- 回転対称性を有し、シリカを主成分とし、少なくとも外周部分に気泡を含有する基体と、該基体の内表面上に形成された、透明シリカガラスからなる内層とを具備するシリカ容器の製造方法であって、少なくとも、
前記基体を形成するための原料粉として、粒径が10~1000μmであり、含有するLi、Na、Kの合計濃度が50wt.ppm以下であるシリカ粉を作製する工程と、
前記内層を形成するための原料粉として、粒径が10~1000μmであり、Ca、Sr、Baの少なくとも1種を合計で50~2000wt.ppm含有するシリカ粉を作製する工程と、
前記基体形成用原料粉を型枠内に投入して、該型枠を回転させつつ所定形状に仮成形して基体の仮成形体とする工程と、
前記基体の仮成形体の内表面上に、前記内層形成用原料粉を導入し、前記基体の仮成形体の内表面に応じた所定形状に仮成形して内層の仮成形体とする工程と、
水素若しくはヘリウム又はそれらの混合ガスを10vol.%を超える比率で含有するガス雰囲気にて、放電加熱溶融法により前記基体と内層の仮成形体の内側から加熱することによって、前記基体の仮成形体の外周部分を焼結体とするとともに、前記基体の仮成形体の内周部分及び前記内層の仮成形体を溶融ガラス体とし、前記基体と前記内層とを形成する工程と
を含むことを特徴とするシリカ容器の製造方法。
- 回転対称性を有し、シリカを主成分とし、少なくとも外周部分に気泡を含有する基体と、該基体の内表面上に形成された、透明シリカガラスからなる内層とを具備するシリカ容器の製造方法であって、少なくとも、
前記基体を形成するための原料粉として、粒径が10~1000μmであり、含有するLi、Na、Kの合計濃度が50wt.ppm以下であるシリカ粉を作製する工程と、
前記内層を形成するための原料粉として、粒径が10~1000μmであり、Ca、Sr、Baの少なくとも1種を合計で50~2000wt.ppm含有するシリカ粉を作製する工程と、
前記基体形成用原料粉を型枠内に投入して、該型枠を回転させつつ所定形状に仮成形して基体の仮成形体とする工程と、
放電加熱溶融法により前記基体の仮成形体の内側から加熱することによって、前記基体の仮成形体の外周部分を焼結体とするとともに、前記基体の仮成形体の内周部分を溶融ガラス体とし、前記基体を形成する工程と、
前記形成した基体の内側から前記内層形成用原料粉を散布しつつ、水素若しくはヘリウム又はそれらの混合ガスを10vol.%を超える比率で含有するガス雰囲気にて、放電加熱溶融法により内側から高温加熱することによって、前記基体の内表面上に前記内層を形成する工程と
を含むことを特徴とするシリカ容器の製造方法。
- 前記放電加熱溶融法による工程のうち少なくとも一つを、前記型枠を通じて前記基体又は前記基体の仮成形体の外側から減圧しながら行うことを特徴とする請求項1又は請求項2に記載のシリカ容器の製造方法。
- 前記内層形成用原料粉を、Baを100~1000wt.ppmの濃度で含有し、Alを10~100wt.ppmの濃度で含有するものとすることを特徴とする請求項1ないし請求項3のいずれか一項に記載のシリカ容器の製造方法。
- 前記水素若しくはヘリウム又はそれらの混合ガスを含有するガス雰囲気を、露点温度15℃~-15℃に設定し、該設定した露点温度の±2℃の範囲に制御することを特徴とする請求項1ないし請求項4のいずれか一項に記載のシリカ容器の製造方法。
- 前記水素若しくはヘリウム又はそれらの混合ガスを含有するガス雰囲気を、水素若しくはヘリウム又はそれらの混合ガスの含有比率が100vol.%のものとすることを特徴とする請求項1ないし請求項5のいずれか一項に記載のシリカ容器の製造方法。
- 回転対称性を有し、シリカを主成分とし、外周部分に気泡を含有し、内周部分に透明シリカガラスを含む基体と、該基体の内表面上に形成された、透明シリカガラスからなる内層とを具備するシリカ容器であって、
前記基体は、Li、Na、Kの合計濃度が50wt.ppm以下であり、前記基体の内周部分の透明シリカガラスから切り出した厚さ10mmの両面平行光学研磨試料の光波長600nmにおける直線透過率が91.8~93.2%であり、
前記内層は、Li、Na、Kの合計濃度が100wt.ppb以下であり、Ca、Sr、Baの少なくとも1種を合計濃度50~2000wt.ppmで含有するものであり、該内層から切り出した厚さ10mmの両面平行光学研磨試料の光波長600nmにおける直線透過率が91.8~93.2%であり、該内層から切り出した試料を真空下にて1000℃に加熱したときの水分子の放出量が2×1017分子/g未満であることを特徴とするシリカ容器。
- 前記内層が、Baを100~1000wt.ppmの濃度で含有し、Alを10~100wt.ppmの濃度で含有するものであることを特徴とする請求項7に記載のシリカ容器。
- 前記内層は、OH基を1~50wt.ppm含有し、Li、Na、Kの各濃度が20wt.ppb以下であり、Ti、Cr、Mn、Fe、Ni、Cu、Zn、Zr、Mo、Wの各濃度が10wt.ppb以下であることを特徴とする請求項7又は請求項8に記載のシリカ容器。
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2011032147A (ja) * | 2009-08-05 | 2011-02-17 | Shinetsu Quartz Prod Co Ltd | シリカ容器及びその製造方法 |
US20140283737A1 (en) * | 2012-01-13 | 2014-09-25 | Shin-Etsu Quartz Products Co., Ltd. | Single-crystal silicon pulling silica container and method for producing the same |
US9376761B2 (en) * | 2012-01-13 | 2016-06-28 | Shin-Etsu Quartz Products Co., Ltd. | Single-crystal silicon pulling silica container and method for producing the same |
Also Published As
Publication number | Publication date |
---|---|
US20110272322A1 (en) | 2011-11-10 |
CN102301041A (zh) | 2011-12-28 |
KR101333190B1 (ko) | 2013-11-26 |
CN102301041B (zh) | 2014-05-07 |
US9403620B2 (en) | 2016-08-02 |
EP2511402A4 (en) | 2017-06-07 |
EP2511402A1 (en) | 2012-10-17 |
JP4951057B2 (ja) | 2012-06-13 |
JP2011121811A (ja) | 2011-06-23 |
TW201119957A (en) | 2011-06-16 |
US20130248408A1 (en) | 2013-09-26 |
KR20110110250A (ko) | 2011-10-06 |
TWI405728B (zh) | 2013-08-21 |
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