US20030040423A1 - Higly durable silica glass, process and apparatus for producing same, and member and apparatus provided with same - Google Patents

Higly durable silica glass, process and apparatus for producing same, and member and apparatus provided with same Download PDF

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Publication number
US20030040423A1
US20030040423A1 US10/105,270 US10527002A US2003040423A1 US 20030040423 A1 US20030040423 A1 US 20030040423A1 US 10527002 A US10527002 A US 10527002A US 2003040423 A1 US2003040423 A1 US 2003040423A1
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United States
Prior art keywords
zirconium
silica glass
finely divided
highly durable
silica
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US10/105,270
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English (en)
Inventor
Yoshinori Harada
Shuzo Mizutani
Shinkichi Hashimoto
Masakazu Kudoh
Naoki Miura
Katsufumi Takahashi
Hideki Kiyohara
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Tosoh Quartz Corp
Tosoh Corp
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Tosoh Corp
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Priority claimed from JP2001166307A external-priority patent/JP2002356335A/ja
Priority claimed from JP2001166311A external-priority patent/JP2002356339A/ja
Application filed by Tosoh Corp filed Critical Tosoh Corp
Assigned to TOSOH QUARTZ CORPORATION, TOSOH CORPORATION, TOSOH SGM CORPORATION reassignment TOSOH QUARTZ CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HARADA, YOSHINORI, HASHIMOTO, SHINKICHI, KIYOHARA, HIDEKI, KUDOH, MASAKAZU, MIURA, NAOKI, MIZUTANI, SHUZO, TAKAHASHI, KATSUFUMI
Publication of US20030040423A1 publication Critical patent/US20030040423A1/en
Priority to US10/718,575 priority Critical patent/US7064094B2/en
Abandoned legal-status Critical Current

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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
    • C03B19/01—Other methods of shaping glass by progressive fusion or sintering of powdered glass onto a shaping substrate, i.e. accretion, e.g. plasma oxidation deposition
    • 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
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B19/00—Other methods of shaping glass
    • C03B19/14—Other methods of shaping glass by gas- or vapour- phase reaction processes
    • C03B19/1415—Reactant delivery systems
    • C03B19/1423—Reactant deposition burners
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B19/00—Other methods of shaping glass
    • C03B19/14—Other methods of shaping glass by gas- or vapour- phase reaction processes
    • C03B19/1453—Thermal after-treatment of the shaped article, e.g. dehydrating, consolidating, sintering
    • 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
    • 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
    • C03B2201/07—Impurity concentration specified
    • 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
    • C03B2201/32—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with aluminium
    • 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
    • C03B2201/34—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with rare earth metals, i.e. with Sc, Y or lanthanides, e.g. for laser-amplifiers
    • 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
    • C03B2201/40—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn
    • 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
    • C03C2201/34—Doped silica-based glasses containing metals containing rare 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
    • C03C2201/34—Doped silica-based glasses containing metals containing rare earth metals
    • C03C2201/3411—Yttrium
    • 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
    • C03C2201/40—Doped silica-based glasses containing metals containing transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn
    • 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
    • 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

  • This invention relates to highly durable silica glass, and a process and an apparatus for producing the highly durable silica glass.
  • the highly durable silica glass contains a plasma resistance-enhancing element substantially uniformly dispersed therein and exhibits an enhanced resistance to plasma applied in an apparatus using a plasma such as a semiconductor-production apparatus or a liquid crystal-production apparatus.
  • This invention further relates to a member such as a vessel for a semiconductor, a tool or jig, or a bell jar for a plasma etcher, which member is provided in a semiconductor production apparatus or a liquid crystal production apparatus; and to a semiconductor production apparatus or a liquid crystal production apparatus.
  • a member such as a vessel for a semiconductor, a tool or jig, or a bell jar for a plasma etcher, which member is provided in a semiconductor production apparatus or a liquid crystal production apparatus; and to a semiconductor production apparatus or a liquid crystal production apparatus.
  • a production apparatus using a plasma is widely used, for example, as a semiconductor production apparatus and a liquid crystal production apparatus.
  • a dry etching technique using a plasma a halogen-containing compound gas such as a fluorine-containing compound gas or a chlorine-containing compound gas must be used.
  • a halogen-containing compound gasand its plasma are widely used, for example, as etching gas for dry etching or as cleaning gas in a thermochemical vapor deposition process.
  • halogen-containing compound gas include, for example, fluorine-containing compound gas such as HF, CF 4 , CHF 3 and NF 3 , chlorine-containing compound gas such as Cl 2 , HCl, BCl 3 and CCl 4 , and bromine-containing compound gas such as Br 2 and HBr.
  • fluorine-containing compound gas such as HF, CF 4 , CHF 3 and NF 3
  • chlorine-containing compound gas such as Cl 2 , HCl, BCl 3 and CCl 4
  • bromine-containing compound gas such as Br 2 and HBr.
  • a silica glass-member is popularly equipped.
  • a bell jar or a focus ring which is made of transparent silica glass is used.
  • a raw material for silica i.e., a high-purity quartz powder in not expensive and silica glass is easy to machine and is easily molten by oxyhydrogen flame. Therefore, a shaped high-purity silica glass article having a complicated shape can be produced with a low production cost. Further, silica glass exhibits enhanced high-frequency transmittance.
  • a silica glass member has a problem in durability. That is, when a silica glass member is repeatedly exposed to a halogen-containing compound gas or a plasma thereof, the surface layer thereof is gradually etched and the section thickness is reduced.
  • a fluorine-containing plasma such as CF 4 /O 2 is used, silicon in the silica glass is allowed to react with fluorine radical to form SiF 4 which is evaporated.
  • the reduction of section thickness shortens the service life of silica glass member and tends to cause abnormal discharge.
  • a hlgh-purity opaque silica glass is used because of excellent heat insulation.
  • a conventional opaque silica glass has fine bubbles formed therein for enhancing opaqueness and thus, the surface is rough, and the silica glass has poor sealability and poor toughness and exhibits poor impact resistance when it is exposed to plasma etching gas at high temperature.
  • an object of the present invention is to provide silica glass exhibiting improved durability while high purity, good machinability and reduced production of a powdery substance are maintained, which suitable as a member equipped in an apparatus using a halogen-containing compound gas and its plasma such as a semiconductor-production apparatus or a liquid crystal apparatus.
  • Another object of the present invention is to provide a process for producing a rod of highly durable silica glass, by which a rod of the highly durable silica glass can be efficiently produced.
  • Still another object of the present invention is to provide an apparatus used for the highly durable silica glass rod.
  • a further object of the present invention is to provide a silica glass member made of the highly durable silica glass and suitable for a device such as a vessel for semiconductor, a jig and a tool, and a bell jar for a plasma etcher, used in an apparatus using a halogen-containing compound gas and its plasma, such as a semiconductor-production apparatus or a liquid crystal-production apparatus.
  • a further object of the present invention is to provide a semiconductor-production apparatus or a liquid crystal-production apparatus, which is equipped with a silica glass member made of the above-mentioned highly durable silica glass.
  • highly durable silica glass comprising 0.01% to 2% by weight, based on the weight of the silica glass, of at least one element selected from the group consisting of magnesium, calcium, strontium, barium, yttrium, hafnium and zirconium.
  • a silica glass member for use in an apparatus using a halogen-containing compound gas and a plasma thereof; said member being made of the above-mentioned highly durable silica glass.
  • a semiconductor-production apparatus equipped with a silica glass member made of the above-mentioned highly durable silica glass.
  • a liquid crystal-production apparatus equipped with a silica glass member made of the above-mentioned highly durable silica glass.
  • a process fnr producing a highly durable silica glass ingot comprising simultaneously falling a finely divided silica powder and a finely divided zirconium-containing substance in a furnace using oxyhydrogen flame as heat source to form an accumulated layer of zirconium-containing silica on a bottom of the furnace; and extending the accumulated layer outwardly in radial directions, to form an ingot wherein zirconium is uniformly dispersed in a silica glass matrix.
  • an apparatus for producing a highly durable silioa glass ingot comprised of silica and zirconium, wherein zirconium is uniformly dispersed in a silica glass matrix said apparatus comprising (i) a furnace rotatable round its own axis, (ii) a feed means for allowing a finely divided silica powder and a finely divided zirconium-containing substance to simultaneously fall within the furnace, said feed means being fitted on a top of the furnace; and (iii) a burner for projecting oxyhydrogen flame, said burner being fitted on a top of the furnace.
  • a process for producing a highly durable silica glass ingot comprising allowing a powdery material comprising a. finely divided silica powder and a finely divided zirconium-containing substance to pass through a plasma arc-coupled region whereby the powdery mixture is molten; and collecting the molten material; said plasma arc-coupled region being formed by coupling at least two plasma arcs generated by at least two electrodes having different polarities.
  • FIG. 1 is a schematic illustration of section of a furnace used for producing an ingot of zirconium-containing silica glass of the present invention
  • FIG. 2 is a schematic illustration of section of another furnace used for producing an ingot of zirconium-containing silica glass of the present invention
  • FIG. 3 is a perspective view of a feed means provided in an apparatus for producing an ingot of zirconium-containing silica glass of the present invention
  • FIG. 4A is a sectional view of a burner provided in an apparatus for producing an ingot of zirconium-containing silica glass of the present invention
  • FIG. 4B is a sectional view of another burner provided in an apparatus for producing an ingot of zirconium-containing silica glass of the present invention.
  • FIG. 5 is a partly sectional elevation of an apparatus using plasma melting for producing an ingot of zirconium-containing silica glass of the present invention
  • FIG. 6 is an enlarged schematic view illustrating growth of zirconium-containing silica glass
  • FIG. 7 is an enlarged partially sectional view of a plasma anode torch used in an apparatus using plasma melting for producing an ingot of zirconium-containing silica glass of the present invention
  • FIG. 8 to an enlarged partially sectional perspective illustration of a plasma cathode torch used in an apparatus using plasma melting for producing an ingot of zirconium-containing silica glass of the present invention.
  • FIG. 9 is a partly sectional elevation of an apparatus using plasma melting for producing an ingot of zirconium-containing silica glass of the present invention.
  • the highly durable silica glass of the invention contains 0.01% to 2% by weight, based on the weight of the highly durable silica glass, of at least one element selected from the group consisting of magnesium, calcium, strontium, barium, yttrium, hafnium and zirconium (which element is hereinafter referred to “additive element” when appropriate).
  • the additive element has a function of enhancing the durability of silica glass as used while the silica glass is exposed to a halogen-containing compound gas and its plasma. More specifically, a halogenated compound of the additive element has a sublimation temperature and a boiling point, both of which are much higher than those of a halogenated compound of SiO 2 , i.e., SiCl 4 . Therefore, the rate of sublimation of the halogenated compound of additive element under vacuum is much smaller than that of the halogenated compound of silica glass. Further, the additive element exhibits a rate of etching greatly lower than that of silica glass.
  • the additive element when the additive-containing silica glass is exposed to a halogen-containing compound gas and its plasma over a long period of time, the additive element is etched only at a much lower rate than that of silica glass. Thus, the additive element is gradually deposited on the surface or the concentration of additive element is increased with a progress of etching. The deposited or concentrated additive element prevents the silica glass from being brought into contact with a halogen-containing compound gas and its plasma with the results that the durability of silica glass as used in a halogen-containing compound gas and its plasma is enhanced.
  • zirconium is especially preferable because its oxide is very stable and a zirconium-containing silica glass gives a baneful influence only to a minimum extent during the process of producing semiconductor.
  • the content of additive element in the silica glass of the invention is in the range of 0.01% to 2 by weight, preferably 0.05% to 0.5% by weight, based on the weight of the additive-containing silica glass.
  • the content of additive element is too high, the mechanical strength becomes poor and the silica-glass is liable to be broken at a step of cutting or grinding.
  • zirconium is incorporated, transparency of the silica glass is decreased with an increase of amount of zirconium added.
  • the content of additive element is too low, the durability the durability of silica glass as used in a halogen-containing compound gas and its plasma is not enhanced.
  • the silica glass containing the additive element in the above-mentioned amount exhibits good and well-balanced durability and mechanical strength. Further, when zirconium is incorporated in the above-mentioned range, a a transparent silica glass exhibiting a transmittance of visible light of at least 80% at a thickness of 1 mm can be obtained.
  • the ceramic member comprisesd of an element selected from the above-mentioned additive elements is used as a member in a semiconductor- or liquid crystal-producing apparatus, the ceramic member gives a baneful influence on semiconductor or liquid crystal because it contains sodium and other impurities. Further, the ceramic has grain boundaries and thus erosion occurs at the grain boundaries and grains are liable to be fallen from the ceramic member. Therefore the highly durable silica glass of the present invention is beneficial in this respect as compared with the ceramic member.
  • the highly durable silica glass of the present invention is vitreous.
  • a region surrounding each additive element particle is preferably vitreous, but, only this region may be crystalline.
  • the highly durable silica glass has preferably no bubble nor grain boundary, and is preferably densified. This is because erosion tends to occur at the boundary and bubble with the result of reduction in section thickness and mechanical strength.
  • the additive element is preferably dispersed in a silica glass matrix as uniform as possible for manifesting a maximum durability.
  • zirconium-containing silica glass having a variant coefficient of zirconium concentration as measured on plural micro-regions each having a size of 200 ⁇ m ⁇ 200 ⁇ m by an EPMA (X-ray micro analyzer) in the range of 0.1% to 100% .
  • the variant coefficient is defined by the following equations:
  • ⁇ is standard deviation and C is concentration of zirconium.
  • the measurement is made on, for example, at least five micro-regions, each of which has a size of, for example, 200 ⁇ m ⁇ 200 ⁇ m.
  • the highly durable silica glass of the invention is suitable for use as a member provided in an apparatus using a halogen-containing compound gas and a plasma thereof.
  • the apparatus includes a dry etching apparatus, a semiconductor-producing apparatus and a liquid crystal-producing apparatus.
  • the halogen-containing compound there can be mentioned fluorine-containing compounds such as HF, CF 4 , CHF 3 and NF 3 , chlorine-containing compounds such as Cl 2 , HCl, BCl 3 and CCl 4 , and bromine-containing compounds such as Br 2 and HBr.
  • the shape and surface state of the highly durable silica member is not particularly limited. However, as for a part which is subject to erosion due to a halogen-containing compound gas and its plasma, the part should preferably have a smooth surface, i.e., a reduced surface roughness by polishing or fire polishing
  • the highly durable silica glass of the present invention can be made from a powdery silica material and an additive element-containing compound. More specifically the highly durable silica glass is made by melting together a finely divided powdery silica material and a finely divided additive element-containing substance. A finely divided powdery silica material and a finely divided additive element-containing substance are fed as a mixed powder or separately for melting together. Alternatively, a finely divided powdery silica material having deposited thereon an additive element-containing substance can be used as silica source and additive element source.
  • silica materials such as powdery natural quartz, natural silica, silica sand, ⁇ -quartz and cristobalite, and synthetic silica materials such as those made by a process wherein a silicon alkoxide is hydrolyzed in the presence of hydrochloric acid or an ammonia catalyst, and the obtained silica is calcined; or a process wherein an aqueous alkali metal silicate solution is allowed to react with an acid and the obtained silica is purified and calcined: fumed silica, and soot silica.
  • high-purity silica materials such as silica sand, rock crystal powder, ⁇ -quartz and cristobalite are preferable.
  • the high-purity silica materials preferably have an average particle diameter in the range of 70 ⁇ m to 500 ⁇ m.
  • the synthetic silica preferably has a particle diameter distribution ranging from 40 ⁇ m to 430 ⁇ m and a mode diameter of about 220 ⁇ m because good compactness is obtained and dusting is minimized.
  • the powdery silica materials can be classified into a narrower particle diameter. For example, classified particles with particle diameter distribution ranging from 200 ⁇ m to 300 ⁇ m and a mode diameter of about 260 ⁇ m; or classified particles with particles diameter distribution not larger than 200 ⁇ m and a mode diameter of about 180 ⁇ m can be used.
  • the powdery silica materials preferably have uniform pores having a diameter as small as possible in view of dispersibility of an additive element.
  • the additive element-containing compound is used as a finely divided powder or in a form deposited on finely divided powdery silica material.
  • the additive element-containing compound includes those which are capable of being converted to an oxide upon calcination.
  • the additive element-containing compound is a salt such as nitrate, chloride or sulfate,
  • Finely divided powdery silica material having deposited thereon the additive element-containing compound is prepared, for example, by dissolving a salt of an additive element in water or other liquid medium to prepare a solution, or dispersing an oxide of an additive element to prepare a slurry, and then incorporating powdery silica material in the solution or slurry, followed by evaporating the liquid medium from the solution or slurry with stirring.
  • the thus-prepared powdery silica material has a salt or oxide of the additive element deposited on fine silica particles.
  • an oxide of the additive element is not thoroughly mixed with powdery silica material and is agglomerated in the slurry, the oxide of additive element is not uniformly deposited on the fine silica particles, and the resulting highly durable silica glass is liable to have poor transparency.
  • a trace amount of an element other than the above-mentioned additive elements can be used in combination with an additive element-containing compound and a finely divided silica powder.
  • a trace amount of aluminum can be used.
  • zirconium When zirconium is used as an additive element, transparency of the highly durable silica glass is liable to be reduced with an increase in amount of zirconium, and the silica glass is not suitable for sight glass.
  • a solid solution of zirconium in silica glass must be formed by employing a high melting temperature of at least 2, 150° C. The solid solution can also be formed by enhancing the contact area Qf zirconium with silica or by incorporating a trace amount of aluminum.
  • the highly durable silica glass is made by melting together a finely divided powdery silica material and a finely divided zirconium-containing substance.
  • the melting method includes an oxyhydrogen flame melting method, a plasma melting method or an electrical melting method.
  • a furnace using oxyhydrogen flame as heat source and preferably capable of being rotated is used. That is, a finely divided silica powder and a finely divided zirconium-containing substance are simultaneously fallen in a furnace using oxyhydrogen flame as heat source to form an accumulated layer of zirconium-containing silica on a bottom of the furnace; and extending the accumulated layer outwardly in radial directions, to form an ingot wherein zirconium is uniformly dispersed in a silica glass matrix.
  • the finely divided silica powder and the finely divided zirconium-containing substance are fallen as a mixture of the silica powder and the zirconium-containing substance, or separately. Alternatively, a finely divided silica powder having deposited thereon a zirconium-containing substance is fallen.
  • the fallen finely divided silica powder and zirconium-containing substance are contacted with oxyhydrogen flame to form an accumulated layer of molten zirconium-containing silica on a bottom of a furnace, and the accumulated zirconium-containing silica layer is maintained at a temperature sufficiently high for keeping the accumulated zirconium-containing silica layer in a molten stats to be thereby extended outwardly in radial directions.
  • the finely divided silica powder used as silica source in the oxyhydrogen flame melting method is preferably a finely divided powder of high-purity silicon oxide. More preferably the finely divided silica powder is a finely divided powder of high-purity silicon oxide selected from silica sand, rock crystal powder, ⁇ -quartz and cristobalite,
  • the zirconium-containing substance is preferably selected from metallic zirconium, and zirconia and other zirconium compounds. Of these, zirconia is preferable.
  • zirconium compounds there can be mentioned zirconium salts such as zirconium chloride, zirconium nitrate and zirconium oxychloride; zirconia made by a process wherein zircon sand is purified, the resulting zirconium oxychloride is dissolved in pure water, and the aqueous solution is dried and then calcined; zirconia made by a process wherein zirconium hydroxide is calcined; and zirconia made by a hydrolyzing method. Of these, zirconia made by a hydrolyzing method is especially preferable.
  • the finely divided zirconium-containing substance preferably has an average particle diameter in the range of 0.1 ⁇ m to 300 ⁇ m.
  • the amount of finely divided zirconium-containing substance used is such that the weight of zirconium is in the range of 0.01% to 2% by weight, based on the weight of the sum of the finely divided silica powder and the finely divided zirconium-containing substance.
  • FIG. 1 is a schematic illustration of section of a furnace used for producing an ingot of zirconium-containing silica glass of the present invention by the oxyhydrogen flame method
  • FIG. 2 is a schematic illustration of section of another furnace used for producing the zirconium-containing silica glass ingot of the present invention by the oxyhydrogen flame method.
  • a furnace 1 used is rotatable round its own axis. More specifically, a frame 12 supporting the furnace 1 is rotated by a motor. Alumina bricks 8 are laid on the frame 12 . Silicon carbide bricks 11 form a side-wall defining the outer configuration of an ingot of highly durable silica glass of the present invention. The side-wall 11 is surrounded by porous alumina bricks 9 and the alumina bricks 8 for heat insulation.
  • the upper end of furnace 1 is open, and a lid 2 is placed on the upper end edge of furnace 1 with a gap a between the upper end edge of furnace 1 and the lid 2 .
  • the lid 2 is made of heat-resistant bricks such as alumina bricks, porous bricks or zirconia bricks.
  • the lid 2 has a hole for fitting the burner assembly 6 therein and a peep hole (not shown).
  • magnesia bricks such as MgO-Al 2 O 3 bricks and basic refractories such as CaO cannot be used because these materials do not have heat-resistance sufficient for withstanding a high temperature at which zirconium-containing silica glass is melted, or these materials react with molten silica glass.
  • Neutral refractories such as Al 2 O 3 , bricks have high heat resistance, but are not used as refractory placed in contact with molten silica glass because of reactivity with molten silica glass.
  • Silicon carbide refractory has high heat resistance and high mechanical strength, and silica glass can be easily separated therefrom. Therefore, silicon carbide refractory is suitable for side-wall 11 which is directly in contact with molten silica glass.
  • Silicon carbide bricks made with a silicon oxide (SiO 2 ) binder or a silicon nitride (Si 3 N 4 ) binder are preferable.
  • Silicon carbide bricks made with a silicon nitride (Si 3 N 4 ) binder i.e., silicon nitride-bound silicon carbide bricks comprised of 80% by weight of SiO 2 and 20% by weight of Si 3 N 4 are especially preferable.
  • the refractory bricks used for the furnace 1 are preferably baked prior to the fitting in furnace 1 so that metal impurities and fine fragments on the brick surface are removed. If fine fragments remain on the brick surface, minute bubbles are formed within molten silica glass, and the resulting zirconium-containing silica glass becomes opaque.
  • zirconia bricks such as ZrO 2 -SiO 2 bricks are preferably used as material 10 constituting the surface of furnace bottom.
  • zirconia bricks are liable to react with molten silica and sometimes give a cracked ingot or an ingot becomes difficult to separate from the furnace. Therefore the surface of furnace bottom material 10 is preferably covered with heat-resistant zirconia particles (not shown) having a diameter in the range of 2 mm to 10 mm so that a zirconium-containing silica is not directly contacted with the bricks on the bottom and the zirconium-containing silica glass can be easily separated from the furnace.
  • the thickness of the heat-resistant zirconia particles may be varied depending upon the state of the bottom surface, but is usually about 10 mm.
  • An accumulated layer of molten zirconium-containing silica formed on the furnace bottom is maintained at a temperature sufficiently high for extending the molten silica outward in radial directions by heat of oxyhydrogen flame.
  • an auxiliary burner 62 is provided in addition to the main burner assembly 61 in the lid of furnace for giving heat sufficient for extending the molten ziconium-containing silica outward in radial directions. If desired, two or more auxiliary burner may be provided.
  • the direction in which oxyhydrogen flame of the auxiliary burner 62 is directed may not be vertical but is chosen so that uniform temperature distribution is obtained over the entire furnace.
  • the auxiliary burner 62 is preferably inclined by 5 to 15 degrees from the vertical axis in a fashion such that the lower end of auxiliary burner 62 is directed forward in the rotating direction, to avoid disturbance of burnt gas.
  • FIG. 3 is a perspective view of a powder feed means for allowing a finely divided silica powder and a finely divided zirconium-containing substance to simultaneously fall within the furnace 1 .
  • the powder feed means is provided above the furnace 1 so that the lower end of the powder feed means is combined in a burner assembly 6 .
  • the powder feed means comprises at least one powder feed assembly 7 .
  • the or each powder feed assembly 7 comprises, as illustrated in FIG. 3, a powder feed hopper 3 for feeding a powdery material which is the finely divided silica powder or the finely divided zirconium-containing substance or a mixture of the two powders, or a zirconium-containing substance-deposited finely divided silica powder.
  • the powder feed hopper 3 is oscillated so as to avoid blockage of the hopper with powder.
  • the powder feed hopper 3 has an opening 30 at the lower end thereof. The size of opening 30 is variable so that the fed rate of powder is controlled.
  • the powder feed assembly 7 further comprises a rotatable table 31 for receiving the powdery material fed through the opening 30 of the powder feed hopper 3 . On the rotatable table 31 , an equalizer 32 for extending and making uniform in height a heap of the powdery material is fitted. There is a gap between the lower edge of equalizer 32 and the upper surface of table 31 . The size of gap is
  • the powdery material fed from the hopper 3 forms a heap on the table 31 , which impinges on the equalizer 32 whereby the heap of powdery material is extended and its height is made uniform.
  • An excessive portion of the powdery material (not shown) is fallen from the outer periphery of table into a hopper 4 for recovery, and then is returned to the hopper 3 .
  • a scraper 33 is provided downstream from the equalizer 32 on the table 31 whereby the powdery material having a uniform height is moved outward along the length of scraper 33 and fallen from the table 31 into a hopper 5 .
  • the scraper 33 extends from the vicinity of the center of table 31 to the outer periphery of table 31 .
  • the amount of powdery material fallen into the hopper 5 is monitored by a dotting recorder, and is controlled by varying the length of scraper 33 , the rate of rotation of table 31 , and the gap between the lower edge of equalizer 32 and the upper surface of table 31 .
  • the powdery material fallen into the hopper 5 is fed to the burner assembly 6 shown in FIG. 1.
  • the feed rate of powdery material is usually in the range of 0.1 kg/hr to 10 kg/hr, preferably 0.3 kg/hr to 3 kg/hr.
  • the powdery material is a mixture of a finely divided silica powder and finely divided zirconium-containing substance, or a finely divided silica powder having deposited thereon finely divided zirconium-containing substance
  • a single powder feed assembly 7 is used.
  • a finely divided silica powder and finely divided zirconium-containing substance are separately fed to the burner assembly 6 , two powder feed assemblies are used,
  • FIG. 4A is a sectional view of a burner assembly fitted to the lid of a furnace using oxyhydrogen flame, wherein a finely divided silica powder having deposited thereon a finely divided zirconium substance is fed.
  • FIG. 4B is a sectional view of another burner assembly fitted to the lid of a furnace using oxyhydrogen flame, wherein a finely divided silica powder and, a finely divided zirconium substance are separately fed.
  • FIG. 4A hydrogen 40 and oxygen 41 are supplied through separate pipes into the burner assembly.
  • a finely divided silica powder having deposited thereon a finely divided zirconium substance 42 is supplied together with a carrier gas 43 .
  • FIG. 4B hydrogen 40 and oxygen 41 are supplied through separate pipes into the burner assembly.
  • a finely divided silica powder 45 is supplied together with a carrier gas 43
  • a finely divided zirconium substance 44 is supplied together with a carrier gas 43 .
  • the burner assembly is fitted to the lid of furnace in a fashion that the lower end of burner assembly is downward projected (FIG. 1 and FIG. 2)
  • the lid 2 is placed on the furnace 1 with a gap a between the upper end edge of furnace 1 and the lid 2 , and therefore the lid 2 is independent from rotation of the furnace 1 .
  • the lid 2 has one or more holes for fitting the burner assembly 6 or 61 and optional burner 62 therein and a peep hole (not shown).
  • the burner assembly 6 or 61 is connected through a feeding pipe (not shown) to a hopper 5 of a powdery material feed means 7 (shown in FIG. 3).
  • the burner assembly 6 or 61 receives a powdery material through the feeding pipe from the hopper 5 of the powdery material feed means.
  • a means for oscillating the feeding pipe is preferably provided so as to avoid blockage of the feeding pipe.
  • the burner assembly 6 or 61 and the optional auxiliary burner 62 are ignited and the furnace 1 is rotated round its axis at a revolution rate in the range of 2 to 10 rpm.
  • the furnace 1 is preferably pre-heated for 1 to 24 hours, more preferably 3 to 5 hours to remove impurities and fine fragments from the brick surfaces as mentioned above,
  • the powdery material feed means 7 (shown in FIG. 3).is operated to feed a silica powder having deposited thereon a zirconium-containing substance, or a mixture of a silica powder and a zirconium-containing substance, or a silica powder and a zirconium-containing substance separately to the main burner assembly 6 or 61 , from which the powdery material is fallen to the furnace bottom while being melted.
  • the accumulated molten zirconium-containing silica is extended outwardly in radial directions.
  • the central part within the furnace 1 is maintained at a temperature of about 2,000° C., namely, higher than the melting point of silica glass, by the burner assembly 6 or 61 and the optional auxiliary burner 62 , and further, the furnace 1 is rotated. Therefore, with an increase in height of the accumulated molten zirconium-containing silica, it is extended outwardly in radial directions. Thus, a zirconium-containing silica glass wherein zirconium is uniformly dispersed and which has no or only a trace amount of minute bubbles can be produced.
  • the distance between the burner assembly 6 or 61 and the upper surface of the accumulated molten zirconium-containing can be maintained at constant by gradually lowering the furnace 1 .
  • the furnace 1 can be rotated around its own axis located in the center or a vicinity thereof, whereby the furnace 1 is moved by about 50 mm to 150mm in the horizontal direction.
  • the molten zirconium-containing silica extended outwardly in radial directions reaches the side-wall 11 , and an ingot having a shape defined by the side-wall is obtained.
  • an ingot having a shape defined by the side-wall is obtained.
  • four side-walls of the same size are arranged, an ingot having a cross-section of regular square with a size of 1000 mm ⁇ 1,000 mm and a thickness of 300 mm thickness can be obtained.
  • an ingot having a polygonal or round cross-section can be obtained.
  • a powdery material comprising a finely divided silica powder and a finely divided zirconium-containing substance is allowed to pass through a plasma arc-coupled region whereby the powdery material is molten; and the molten material is collected.
  • the plasma arc-coupled region is formed by coupling at least two plasma arcs generated by at least two electrodes having different polarities.
  • the highly durable zirconium-containing silica glass made by this process is beneficial in that segregation of zirconium is not found in the zirconium-containing silica glass and the zirconium-containing silica glass has no or only trace amount of fine bubbles and impurities.
  • the powdery material used in this process includes a mixture of a finely divided silica powder and a finely divided zirconium-containing substance, and a finely divided silica powder having deposited thereon a finely divided zirconium-containing substance,
  • the finely divided silica powder used as silica source in the plasma melting method is preferably a finely divided powder of high-purity silicon oxide. More preferably, the finely divided silica powder is a finely divided powder of high-purity silicon oxide selected from silica sand, rock crystal powder, ⁇ -quartz and cristobalite.
  • the finely divided zirconium- containing substance preferably has an average particle diameter in the range of 0.1 ⁇ m to 300 ⁇ m, more preferably 10 ⁇ m to 80 ⁇ m.
  • the amount of finely divided zirconium-containing substance used is such that the weight of zirconium is in the range of 0.01% to 2% by weight, preferably 0.05% to 0.5% by weight, based on the weight of the sum of the finely divided silica powder and the finely divided zirconium-containing substance. If the zirconium content is smaller than 0.01 by weight, a desired plasma resistance cannot be obtained. In contrast, if the zirconium content exceeds 2% by weight, the zirconium-containing silica glass becomes opaque and has an undesirable surface configuration leading to reduction of impact resistance and mechanical strength.
  • the zirconium-containing substance used is preferably the same as those mentioned above as for the oxygen flame melting method. That is, the zirconium-containing substance is selected from metallic zirconium, and zirconia and other zirconium compounds. Of these, zirconia is preferable,
  • the electrodes generating plasma arcs are arranged symmetrically and inclined relative to a path of the powdery material in a fashion that plasma arc-generating tips of the electrodes are inwardly directed, wherein the inclination angle of each electrode and the distance from the plasma arc-coupled region to the collected molten material are capable of being independently varied so that transmittance of a resulting highly durable silica glass ingot can be controlled.
  • At least one of the electrodes functions as a cathode and the other electrode or electrodes function as an anode.
  • the cathode and the anode are inclined preferably to an extent such that an inclination angle from the perpendicular axis is in the range of 45 to 65 degrees or the angle between the cathode and the anode is in the range of 80 to 130 degrees.
  • the distance between the tips of cathode and anode is maintained within 100 mm, or the distance from the plasma arc-coupled region to the collected molten material is maintained within 100 mm, whereby a highly durable opaque silica glass ingot is produced. That is, the transparency of zirconium-containing silica glass can be controlled.
  • the thus-obtained opaque silica glass is advantageous over the conventional opaque silica glass which has fine bubbles. That is, the opaque silica glass of the present invention contains no or only a trace amount of fine bubbles and therefore has good. and smooth surface configuration, and the cut surface such as, for example, a sealing surface of the flange part of a bell jar, exhibits good sealability. Further, the opaque silica glass of the present invention exhibits good resistance to plasma and is suitable for use as a member to be exposed to a plasma.
  • the molten material is collected beneficially on a target while the target is rotated round the vertical axis or upwardly moved in the vertical direction, or while the target is rotated round the vertical axis and, simultaneously therewith, is upwardly moved in the vertical direction.
  • a columnar or shell-shaped zirconium-containing silica glass ingot having a large length can be obtained.
  • the highly durable zirconium-containing silica glass made by the plasma melting method is suitable for use as a member to be exposed to high-density halogen-containing gas and its plasma.
  • FIG. 5 which is a partly sectional elevation of an apparatus using the plasma melting method
  • a hopper 101 is charged with a powdery material which is a mixture of a quartz powder having an average particle diameter of about 100 ⁇ M and a metallic zirconium powder having an average particle diameter of 50 ⁇ m (the amount of metallic zirconium powder is 0.67% by weight based on the sum of the quartz powder and the metallic zirconium powder).
  • the hopper 101 is connected to a feed means 102 .
  • the powdery material is supplied from the hopper 101 to the feed means 102 , and then to silica glass feed tubes 103 and 104 .
  • the powdery material passes through the tubes 103 and 104 to a plasma arc-coupled region 105 .
  • Plasma arc is generated by a plasma anode torch 106 and a plasma cathode torch 107 .
  • the plasma anode torch 106 has an electrode exhibiting no ignition loss.
  • the electrode is made of copper or other metal exhibiting no ignition loss.
  • the zirconium-containing silica powder is melted below the plasma arc-coupled region 105 by heat generated by the plasma arc.
  • a target 108 is provided underneath the region 105 .
  • the target 108 is rotatable on the vertical axis by a rotating mechanism 109 .
  • the target 108 is connected through a rotation shaft 110 with a lifting mechanism 111 . Thus the target 108 can be moved upwardly and downwardly, if desired.
  • a supporting member 113 is provided so that the lifting mechanism 111 is stably operated.
  • the distance between the plasma arc-coupled region 105 and the target 108 is in the range of about 1 cm to about 20 cm.
  • the angle between the anode torch 106 and the cathode torch 107 is in the range of 80° to 130°.
  • the anode torch 106 and the cathode torch 107 are in alignment with each other.
  • the angle between the anode torch 106 and the cathode torch 107 is variable, and the anode torch and the cathode torch are upward and downward movable so that registration can be effected.
  • the anode torch 106 and the cathode torch 107 are positioned symmetrically relative to the vertical axis.
  • the position of feed tube 104 also can be varied in a horizontal direction and in the vertical direction.
  • the target is usually rotated at a rate of 1 to 60 rpm.
  • FIG. 6 is an enlarged schematic view illustrating growth of zirconium-containing silica glass
  • a powdery material is fallen through in a tube 113 into a plasma arc-coupled region where a plasma arc 114 generated by the plasma torch 106 and a plasma arc 115 generated by the plasma torch 107 are coupled.
  • the zirconium-containing silica is further fallen to impinge upon the rotating target 108 .
  • a zirconium-containing silica glass ingot 116 is formed on the target 108 .
  • a plasma arc-coupled region is stationarily formed on the zirconium-containing silica glass ingot 116 .
  • the target 108 is downward moved by a lifting mechanism 111 (shown in FIG. 5).
  • the rate of movement is usually in the range of 0.1 cm/min to 5 cm/min.
  • a current of 100 to 500 ampere at a voltage of 50 to 250 V is applied to each of plasma arc torches 114 and 115 .
  • An argon gas is preferably supplied at a flow rate of 10 to 60 liter/min through each of plasma arc torches 114 and 115 .
  • the rate of mixed powder (quartz powder plus metallic zirconium powder) supplied is usually in the range of 0.5 to 20 kg/hour.
  • the nozzle 125 is electrically insulated by an insulating member 129 from an electrode assembly 128 .
  • the round end of the electrode 120 ensures an arc route and enables high-electric current passage and gives enhanced service life. Abrasion of inner wall of the nozzle 125 is minimized and the contamination of zirconium-containing silica glass also is minimized by the round end of electrode 120 .
  • FIG. 8 is an enlarged partially sectional perspective illustration of a plasma cathode torch 126 used in the apparatus using plasma melting method.
  • argon gas flows through a space 136 a surrounding a cathode electrode 134 to form an argon arc which is ejected from a torch nozzle.
  • Nitrogen gas flows through a space 136 b surrounding the cathode electrode 134 and is ejected through small holes 138 .
  • the small holes 138 are radially arranged at the top portion of torch nozzle, and are inwardly directed so that the ejected nitrogen gas streams are converged.
  • the amount of nitrogen gas is usually in the range of 5 to 50%.
  • the ejected nitrogen gas is ionized by argon arc and generates an argon-nitrogen plasma.
  • a plasma arc is formed highly efficiently, and an argon-nitrogen plasma is formed while tungsten constituting the cathode electrode 134 is not contacted with nitrogen gas. Therefore a reaction of tungsten with nitrogen can be avoided and the service life of the cathode electrode is improved.
  • Cooling water is circulated from a space 140 a to a space 140 b for cooling the torch nozzle. Cooling water is circulated from a space 142 a to 142 b for insulating radiant heat from the plasma arc.
  • the zirconium-containing silica glass ingot is produced with enhanced productivity. Further, the zirconium-containing silica glass ingot is not contaminated with fine fragments from the electrode material and has a high purity.
  • FIG. 9 which is a partly sectional elevation of another apparatus using the plasma melting method
  • a hopper 110 is charged with a powdery material which is a mixture of a finely divided silica powder and a finely divided zirconium-containing substance, or a finely divided silica powder having deposited thereon a finely divided zirconium-containing substance.
  • the hopper 130 is connected to a constant-rate feeding means 112 , a connecting tube 114 and a powdery material feeding tube 116 .
  • the powdery material is supplied from the hopper 110 through the feeding means 112 and the connecting tube 114 into a melting vessel 118 within a furnace 120 .
  • the position of melting vessel 118 can be shifted in the vertical direction and in the horizontal direction.
  • a twin plasma torch comprising a plasma anode torch 124 and a plasma cathode torch 126 is arranged in a manner such that the two plasma torches are symmetrically inserted in the furnace 120 relative to a plasma arc-coupled region 122 .
  • the torch angle and the depth of the plasma torches can be controlled.
  • the plasma anode torch 124 and the plasma cathode torch 126 are inclined preferably to an extent such that an inclination angle from the perpendicular axis is in the range of 45 to 65 degrees and the distance in the horizontal direction between the lower ends of the two plasma torches is in the range of 50 to 100 mm.
  • the plasma anode torch 124 has the same structure and function as those explained above in detail with reference to FIG. 7 as to the first embodiment.
  • the plasma cathode torch 126 has the same structure and function as those explained in detail above with reference to FIG. 8 as to the first embodiment.
  • the melting vessel 118 is made of, for example, steel and can be cooled.
  • the melting vessel 118 is supported by a rotating shaft 144 .
  • the melting vessel 118 is rotatable round its central axis.
  • the melting vessel 118 may be eccentrically rotated round an axis slightly displaced from the center of vessel.
  • the rotating shaft 144 is provided in a manner such that it can be rotated by a motor 148 and can be lifted by a motor 150 , which motors are fitted on a furnace base 146 .
  • a rotary joint 154 having a cooling water inlet 152 a and a cooling water outlet 152 b is fitted to the lower end of the rotating shaft 144 , thus cooling water being circulated in the melting vessel 118 .
  • the ceiling part of the furnace 120 is flat and can be cooled by cooling water circulating therein. Silica vapor volatilizing from the molten silica in the melting vessel 118 flows upwardly and is exhausted through outlets 156 provided in side-wall.
  • the bottom surface of the melting vessel 118 is covered with silica particles having a large particle diameter at a thickness of about 1 cm to about 20 cm.
  • the melting of the powdery material is effected in a plasma arc-coupled region 122 where plasma arcs generated from the plasma anode torch 124 and the plasma cathode torch 126 are coupled together to give heat sufficient for melting the powdery material.
  • the angle and position of the plasma anode torch 124 and the plasma cathode torch 126 are adjusted while the melting vessel 118 is rotated at a predetermined rate.
  • the powdery material is fallen through the plasma arc-coupled region 122 to form a small heap of partly melted zirconium-containing silica on the center of the bottom covered with silica particles.
  • the powdery material is continually fallen, while the adjustment of angle and position of the plasma anode torch 124 and the plasma cathode torch 126 are continued, to enlarge the heap of partly melted zirconium-containing silica.
  • the vessel 118 is downward moved so that the heap of partly melted zirconium-containing silica is maintained at a temperature sufficient for keeping a molten state.
  • an electrical melting method can be employed (although not shown in the drawings).
  • a finely divided powdery silica having deposited thereon a finely divided zirconium-containing compound is prepared, for example, by dissolving a salt of zirconium such as nitrate, sulfate or chloride in water or other liquid medium to prepare a solution, or dispersing an oxide of zirconium to prepare a slurry, and then incorporating powdery silica material in the solution or slurry, followed by evaporating the liquid medium at a high temperature from the solution or slurry with stirring.
  • the thus-prepared powdery silica material has a zirconium salt or oxide deposited on fine silica particles.
  • the powdery silica material is calcined at a temperature of 500° C. to 1,000° C. in an electric furnace to prepare a calcined product comprised of silica particles having deposited thereon zirconium oxide particles.
  • the powdery silica material may be molded together with an optional binder such as, for example, an acrylic resin into a molding.
  • the calcined product is then baked at a temperature higher than the calcination temperature but lower than the melting point of cristobalite, namely at a temperature of 1,800° C. to 1,900° C. in an electric furnace to give a highly durable silica glass in which zirconium is uniformly dispersed.
  • the finely divided silica material used includes, for example, natural silica Dowder such as quartz powder, synthetic silica powder, fumed silica powder and soot silica powder.
  • synthetic silica When synthetic silica is used, it preferably has a particle diameter distribution ranging from 40 ⁇ m to 430 ⁇ m and a mode diameter of about 220 ⁇ m because good compactness is obtained and dusting is minimized.
  • the powdery silica materials can be classified into a narrower particle diameter. For example, classified particles with particle diameter distribution ranging from 200 ⁇ m to 300 ⁇ m and a mode diameter of about 260 ⁇ m; or classified particles with particles diameter distribution not larger than 200 ⁇ m and a mode diameter of about 180 ⁇ m are mentioned.
  • the powdery silica materials preferably have uniform pores having a diameter as small as possible in view of dispersibility of an additive element.
  • a three-point bending test was carried out.
  • the as-measured bending strength can be a criterion for processability of silica glass.
  • the test results were evaluated by comparing the bending strength with that of control silica glass having therein no additive element, and expressed by assigning the following three ratings A, B and C. The test results are shown in Table 1.
  • B At least one of the ratings for plasma resistance and bending strength was B.
  • C At least one of the ratings for plasma resistance and bending strength was C.
  • plasma resistance i.e., durability of silica glass containing an additive element is enhanced with an increase in content of the additive element.
  • content of additive element is smaller than 0.01 by weight, the plasma resistance is poor.
  • content of additive element is at least 0.01% by weight, especially at least 0.05% by weight, the plasma resistance is satisfactory.
  • a finely divided quartz powder having an average particle diameter of 200 ⁇ m was thoroughly mixed together with a zirconium oxide having an average particle diameter not larger than 5 ⁇ m. The mixture was melted by oxyhydrogen flame or in an electric furnace under vacuum to give zirconium-containing silica glass.
  • the concentration of zirconium in the mixture was measured by a method wherein the silica glass was dissolved by pressure acidolysis using hydrofluoric acid and the solution was quantitatively analyzed by the ICP atomic emission spectrochemical analysis.
  • a plate having a thickness of 1 mm was prepared from the zirconium-containing silica glass. Both surfaces of the plate were mirror-polished to prepare a sample for testing light transmittance. The sample was irradiated with visible light with a wavelength of 600 nm by using a spectrophotometer “U-320” available from Hitachi, Ltd. to determine percentage of light transmittance. The test results were expressed by assigning the following two ratings.
  • a plate having a slide glass size was out from the additive element-containing silica glass.
  • the plate was mirror-polished and then the polished surface was subjected to masking, Using the thus prepared sample, plasma resistance was tested by the same method as that employed in Examples 1-21. The test results are shown in Table 2.
  • B At least one of the ratings for plasma resistance, bending strength and light transmittance was B.
  • C At least one of the ratings for plasma resistance, bending strength and light transmittance was C.
  • plasma resistance i. e., durability of zirconium-containing silica glass is enhanced with an increase of zirconium content.
  • the zirconium content is smaller than 0.01% by weight, the plasma resistance is poor.
  • the zirconium content is at least 0.01% by weight, especially at least 0.05by weight, the plasma resistance is satisfactory.
  • the zirconium content exceeds about 0.50% by weight, the processability of silica glass is gradually deteriorated.
  • the zirconium content exceeds 2% by weight, the silica glass is liable to be broken at an abrading or polishing step or at a step of welding by oxyhydrogen flame.
  • good and balanced processability and plasma resistance are obtained when the zirconium content is not larger than 2% by weight, more preferably not larger than 0.50by weight.
  • Example 25 The temperature for melting the powdery material within oxyhydrogen flame in Example 24 was difficult to measure. But, the temperature of oxyhydrogen flame used was 2,600° C. and thus, it is believed that the powdery material was melted at this temperature. Where the powdery material was melted in an electric furnace under vacuum, if the zirconium content was 0.57% by weight (Example 25) a satisfactory light transmittance was obtained only when the melting temperature was at least about 2,150° C.
  • TABLE 3 Ingredients Al Ca Cu Fe Na K Li Content 6.9 0.4 ⁇ 0.01 0.1 0.1 0.08 0.2
  • zirconium oxychloride ZrCl 2 O.8H 2 O, purity 99.0%
  • This solution was mixed with the quartz powder and the mixture was allowed to stand for about 1 hour.
  • the mixture was placed in a quartz boat, and heated in the air at 90° C. for 8 hours and then calcined at 500° C. for 1 hour.
  • X-ray diffraction of the calcined product revealed that zirconium oxychloride was substantially converted to zirconia ZrO 2 .
  • the content of zirconium in a silica material to be treated was 5,000 ppm.
  • the calcined product was free-flowing powdery material.
  • a carbon mold composed of high-purity carbon was charged with the powdery material.
  • a packing of charged powdery material had a cylindrical shape having a diameter of 90 mm and a height of 25 mm.
  • the packing was melted in an electric furnace under vacuum. The temperature in the furnace was elevated from room temperature to 1,850° C. at a rate of 5° C./min, and maintained at 1,850° C. for 5 minutes. Thereafter the furnace was cooled in a nitrogen atmosphere.
  • the content of zirconium in the thus-obtained zirconium-containing silica glass was measured by an electron probe micro analyzer. The results are shown in Table 4. TABLE 4 Measurement points 1 2 3 4 5 Zr content (atomic %) 0.527 0.256 0.319 0.443 0.469
  • the average zirconium content was 0.403 atomic %, the standard deviation was 0.112 (atomic %), and the variant coefficient was 28.
  • a plate sample was cut from the zirconium-containing silica glass, and was subjected to plasma etching in a mixed CF 4 /O 2 gas atmosphere or a mixed BCl 3 /Cl 2 gas atmosphere by the same procedure as employed in Examples 1-21 to evaluate plasma resistance.
  • the plasma resistance was better than that of control silica glass containing no zirconium.
  • the average zirconium content was 0.133 atomic %, the standard deviation was 0.013 (atomic %), and the variant coefficient was 10%.
  • a plate sample was cut from the zirconium-containing silica glass, and was subjected to plasma etching in a mixed CF 4 /O 2 gas atmosphere or a mixed BCl 3 /Cl 2 gas atmosphere by the same procedure as employed in Examples 1-21 to evaluate plasma resistance.
  • the plasma resistance was better than that of control silica glass containing no zirconium.
  • a quartz powder containing the ingredients shown in Table 3 in Example 26 and particle diameters ranging from 40 to 430 ⁇ m and a mode diameter of 219 ⁇ m was purified, and 223 g of the quartz powder was weighed.
  • 1.516 g of a zirconium oxide powder having a purity of 99.9 was weighed, and mixed in a dry state with the quartz powder for 2 hours by using a pot mill rotating base.
  • the mixed powder was melted in an electric furnace under vacuum to obtain zirconium-containing silica glass.
  • the content of zirconium in the zirconium-containing silica glass was measured by an electron probe micro analyzer. The results are shown in Table 6.
  • TABLE 6 Measurement points 1 2 3 4 5 Zr content (atomic %) 0.181 0.256 1.319 0.443 3.001
  • the average zirconium content was 1.040 atomic %, the standard deviation was 1.187 (atomic %), and the variant coefficient was 114%.
  • a plate sample was cut from the zirconium-containing silica glass, and was subjected to plasma etching in a mixed CF 4 /O 2 gas atmosphere or a mixed BCl 3 /Cl 2 gas atmosphere by the same procedure as employed in Examples 1-21 to evaluate plasma resistance.
  • the plasma resistance was poor as compared with that of zirconium-containing silica glass in Example 22.
  • a quartz powder containing the ingredients shown in Table 3 in Example 26 and particle diameters ranging from 40 to 430 ⁇ m and a mode diameter of 219 ⁇ m was purified, and 223 g of the quartz powder was weighed.
  • 1.516 g of a zirconium oxide powder having a purity of 99.94 was weighed, and mixed in a dry state with the quartz powder for 4 days by using a pot mill rotating base.
  • the mixed powder was melted in an electric furnace under vacuum to obtain zirconium-containing silica glass.
  • the content of zirconium in the zirconium-containing silica glass was measured by an electron probe micro analyzer. The results are shown in Table 7.
  • TABLE 7 Measurement points 1 2 3 4 5 Zr content (atomic %) 0.231 1.562 3.021 0.006 4.002
  • the average zirconium content was 1.764 atomic %, the standard deviation was 1.737 (atomic %), and the variant coefficient was 98%.
  • a plate sample was cut from the zirconium-containing silica glass, and was subjected to plasma etching in a mixed CF 4 /O 2 gas atmosphere or a mixed BCl 3 /Cl 2 gas atmosphere by the same procedure as employed in Examples 1-21 to evaluate plasma resistance.
  • the plasma resistance was poor as compared with that of zirconium-containing silica glass obtained in Example 22 but it was better than that obtained in Comparative Example 17.
  • Zirconium oxychloride was hydrolyzed by the conventional procedure to prepare a zirconia powder.
  • the zirconia powder was combined with a finely divided quartz powder in a synthetic resin pot and was mixed together by using a ball mill mixer to prepare a powdery quartz/zirconia mixture containing 5,000 ppm of zirconium.
  • FIG. 2 An apparatus shown in FIG. 2 equipped with a main burner assembly and an auxiliary burner, both of which were made of silica glass. was used for melting the powdery quartz/zirconia mixture.
  • the size of a melting chamber defined by silicon carbide bricks within the furnace was 750 mm ⁇ 750 mm ⁇ 400 mm.
  • An additive element such as zirconium is uniformly dispersed in the silica glass.
  • the silica glass exhibits enhanced plasma resistance, i.e., enhanced durability when used as a member in a semiconductor-production apparatus or a liquid crystal-production apparatus.
  • the silica glass has good processability and reduced fly of fine fragments, which are inherently possessed by conventional high-purity silica glass.
  • the silica glass is suitable as a member for use in an apparatus to which high plasma resistance and high heat resistance are required, such as a semiconductor-production apparatus or a liquid crystal-production apparatus.
  • a member for use in an apparatus to which high plasma resistance and high heat resistance are required, such as a semiconductor-production apparatus or a liquid crystal-production apparatus.
  • Such member includes, for example, jigs and tools such as a flange part of a reaction tube and a bell jar.
  • a silica glass ingot having a large size can be advantageously produced by the melting method using oxyhydrogen flame.

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  • Organic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Plasma & Fusion (AREA)
  • Thermal Sciences (AREA)
  • Glass Compositions (AREA)
US10/105,270 2001-03-26 2002-03-26 Higly durable silica glass, process and apparatus for producing same, and member and apparatus provided with same Abandoned US20030040423A1 (en)

Priority Applications (1)

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JP2001087082 2001-03-26
JP2001-87082 2001-03-26
JP2001-166307 2001-06-01
JP2001-166311 2001-06-01
JP2001166307A JP2002356335A (ja) 2001-06-01 2001-06-01 ジルコニウム含有複合石英ガラスの製造方法及び装置
JP2001166311A JP2002356339A (ja) 2001-06-01 2001-06-01 高耐久性石英ガラス部材

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US (2) US20030040423A1 (fr)
KR (1) KR100842232B1 (fr)
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US20160355429A1 (en) * 2006-06-20 2016-12-08 Momentive Performance Materials Inc. Fused quartz tubing for pharmaceutical packaging
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US20160355429A1 (en) * 2006-06-20 2016-12-08 Momentive Performance Materials Inc. Fused quartz tubing for pharmaceutical packaging
US9919948B2 (en) * 2006-06-20 2018-03-20 Momentive Performance Materials, Inc. Fused quartz tubing for pharmaceutical packaging
US20110232847A1 (en) * 2007-08-02 2011-09-29 Heraeus Quarzglas Gmbh & Co. Kg Quartz glass member for plasma etching
US20130239618A1 (en) * 2010-12-02 2013-09-19 Asahi Glass Company, Limited Glass melting furnace, process for modifying glass melt, process for producing glass melt, process for producing glass product, and apparatus for producing glass product
US10024577B2 (en) 2011-09-14 2018-07-17 Heraeus Quarzglas Gmbh & Co. Kg Solar radiation receiver having an entry window made of quartz glass and method for producing an entry window
KR20190135013A (ko) * 2017-04-26 2019-12-05 토소 에스지엠 가부시키가이샤 내자외선성 석영 유리 및 그의 제조 방법
EP3617159A4 (fr) * 2017-04-26 2020-12-30 Tosoh Sgm Corporation Verre de quartz résistant aux ultraviolets et son procédé de fabrication
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Also Published As

Publication number Publication date
US7064094B2 (en) 2006-06-20
US20040116269A1 (en) 2004-06-17
KR100842232B1 (ko) 2008-06-30
DE10213539A1 (de) 2002-10-24
KR20020076183A (ko) 2002-10-09
TWI293947B (fr) 2008-03-01

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