US20040123795A1 - Production apparatus and method of fluoride crystal, and crucible - Google Patents
Production apparatus and method of fluoride crystal, and crucible Download PDFInfo
- Publication number
- US20040123795A1 US20040123795A1 US10/715,453 US71545303A US2004123795A1 US 20040123795 A1 US20040123795 A1 US 20040123795A1 US 71545303 A US71545303 A US 71545303A US 2004123795 A1 US2004123795 A1 US 2004123795A1
- Authority
- US
- United States
- Prior art keywords
- crucible
- crystal
- fluoride
- present
- stage
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000013078 crystal Substances 0.000 title claims abstract description 106
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 title claims abstract description 58
- 238000000034 method Methods 0.000 title claims abstract description 40
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 30
- 239000000463 material Substances 0.000 claims abstract description 63
- 230000008569 process Effects 0.000 claims abstract description 34
- 238000007872 degassing Methods 0.000 claims abstract description 26
- 239000002516 radical scavenger Substances 0.000 claims abstract description 24
- 238000007670 refining Methods 0.000 claims abstract description 24
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 claims description 22
- 229910001634 calcium fluoride Inorganic materials 0.000 claims description 16
- 239000012535 impurity Substances 0.000 abstract description 21
- 230000003287 optical effect Effects 0.000 description 34
- BHHYHSUAOQUXJK-UHFFFAOYSA-L zinc fluoride Chemical compound F[Zn]F BHHYHSUAOQUXJK-UHFFFAOYSA-L 0.000 description 14
- 238000002844 melting Methods 0.000 description 13
- 230000008018 melting Effects 0.000 description 13
- 239000007789 gas Substances 0.000 description 11
- 238000000137 annealing Methods 0.000 description 9
- 238000010586 diagram Methods 0.000 description 7
- 230000007246 mechanism Effects 0.000 description 7
- 239000010436 fluorite Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 238000010298 pulverizing process Methods 0.000 description 5
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 4
- 239000000292 calcium oxide Substances 0.000 description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000005286 illumination Methods 0.000 description 4
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 230000003595 spectral effect Effects 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 239000011810 insulating material Substances 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- BRCWHGIUHLWZBK-UHFFFAOYSA-K bismuth;trifluoride Chemical compound F[Bi](F)F BRCWHGIUHLWZBK-UHFFFAOYSA-K 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000005283 ground state Effects 0.000 description 2
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 2
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- -1 and the like Substances 0.000 description 1
- OYLGJCQECKOTOL-UHFFFAOYSA-L barium fluoride Chemical compound [F-].[F-].[Ba+2] OYLGJCQECKOTOL-UHFFFAOYSA-L 0.000 description 1
- 229910001632 barium fluoride Inorganic materials 0.000 description 1
- LVEULQCPJDDSLD-UHFFFAOYSA-L cadmium fluoride Chemical compound F[Cd]F LVEULQCPJDDSLD-UHFFFAOYSA-L 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000006063 cullet Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000001017 electron-beam sputter deposition Methods 0.000 description 1
- 238000000313 electron-beam-induced deposition Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000005281 excited state Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- YAFKGUAJYKXPDI-UHFFFAOYSA-J lead tetrafluoride Chemical compound F[Pb](F)(F)F YAFKGUAJYKXPDI-UHFFFAOYSA-J 0.000 description 1
- 208000020442 loss of weight Diseases 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229910001936 tantalum oxide Inorganic materials 0.000 description 1
- BYMUNNMMXKDFEZ-UHFFFAOYSA-K trifluorolanthanum Chemical compound F[La](F)F BYMUNNMMXKDFEZ-UHFFFAOYSA-K 0.000 description 1
- XRADHEAKQRNYQQ-UHFFFAOYSA-K trifluoroneodymium Chemical compound F[Nd](F)F XRADHEAKQRNYQQ-UHFFFAOYSA-K 0.000 description 1
Images
Classifications
-
- 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
- C30B11/00—Single-crystal growth by normal freezing or freezing under temperature gradient, e.g. Bridgman-Stockbarger method
- C30B11/002—Crucibles or containers for supporting the melt
-
- 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
- C30B11/00—Single-crystal growth by normal freezing or freezing under temperature gradient, e.g. Bridgman-Stockbarger method
-
- 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
- C30B29/10—Inorganic compounds or compositions
- C30B29/12—Halides
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T117/00—Single-crystal, oriented-crystal, and epitaxy growth processes; non-coating apparatus therefor
- Y10T117/10—Apparatus
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T117/00—Single-crystal, oriented-crystal, and epitaxy growth processes; non-coating apparatus therefor
- Y10T117/10—Apparatus
- Y10T117/1016—Apparatus with means for treating single-crystal [e.g., heat treating]
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T117/00—Single-crystal, oriented-crystal, and epitaxy growth processes; non-coating apparatus therefor
- Y10T117/10—Apparatus
- Y10T117/1024—Apparatus for crystallization from liquid or supercritical state
- Y10T117/1092—Shape defined by a solid member other than seed or product [e.g., Bridgman-Stockbarger]
Definitions
- the present invention relates to a production apparatus of a fluoride crystal preferable for various kinds of optical elements, lens, window materials, prisms, and the like to be used in a wide wavelength range from a vacuum ultraviolet region to a far infrared region, in particular, to a production apparatus of a fluoride crystal to be used for an optical material such as a large aperture lens (aperture of 250 mm or more) for an excimer laser.
- a large aperture lens aperture of 250 mm or more
- An excimer laser attracts attention as the only one high output laser to oscillate outside an ultraviolet region so that the application thereof is expected in the electronic industry, chemical industry, and energy industry.
- the excimer laser is used in processing metal, resin, glass, ceramics and semiconductors, and a chemical reaction.
- An apparatus for generating an excimer laser beam is known as an excimer laser oscillating apparatus.
- a laser gas filled in a chamber, such as Ar, Kr, Xe, F 2 , Cl 2 is excited by the electron beam radiation or the electric discharge.
- the excited atoms bond with atoms in the ground state so as to produce molecules capable of existing only in the excited state.
- the molecules are. the excimer. Due to its instability, the excimer immediately discharges the ultraviolet ray and falls into the ground state. This phenomenon is called the bond free transition.
- An apparatus for taking out a laser beam by amplifying the ultraviolet ray obtained by the transition in an optical resonator comprising a pair of mirrors is an excimer oscillating apparatus.
- a KrF laser and an Arf laser have a wavelength of 248 nm and 193 nm, respectively in a vacuum ultraviolet ray region so that an optical system having a high transmissivity with respect to the wavelength region needs to be used.
- glass materials preferably used in the optical system include fluorides, such as calcium fluoride, magnesium fluoride, barium fluoride, neodymium fluoride, lithium fluoride, and lanthanum fluoride.
- FIG. 11 is a schematic diagram showing the production method of a fluoride crystal initially conducted by the present inventor.
- a powdery material is prepared.
- the material placed in a container is melted, and then cooled.
- solidified agglomerates are pulverized with a stainless steel pulverizer.
- a fluorite block is produced by melting and gradually cooling the pulverized agglomerates placed in a crucible for the crystal growth.
- the process S 2 is conducted for reducing the bulk specific density change before and after melting in the process S 4 , and further, for eliminating impurities in the material.
- a scavenger which is a fluoride of a metal, is added in order to eliminate CaO produced by the reaction between the material (CaF 2 ) and water, and the like, or impurities originally existing in the material.
- a ZnF 2 scavenger reacts with CaO so as to be ZnO and eliminated at the time of melting the crystals.
- the CaO impurities are eliminated so that a fluoride crystal having an excellent transmissivity characteristic can be obtained.
- the fluoride crystal block accordingly obtained is cut in a desired thickness, processed and shaped to be a desired lens shape to be used as an optical material.
- An object of the present invention is to provide a production apparatus of a fluoride crystal capable of producing a fluoride crystal having a high transmissivity, and efficiently eliminating impurities and a scavenger remained in the crystal.
- Another object of the present invention is to provide a production apparatus of a fluoride crystal with a high productivity.
- a first aspect of the present invention is a production apparatus of a fluoride crystal having a crucible divided in a plurality to have multi-stages, to be used for refining a material in a process for refining the material by adding a scavenger in the material.
- a second aspect of the present invention is the production apparatus of a fluoride crystal having a degassing hole on a side wall portion of the crucible.
- a third aspect of the present invention is a crucible having at least two degassing holes on a side wall portion.
- a fourth aspect of the present invention is the crucible having a connecting hole in the bottom center portion, and having at least two degassing holes on a side wall portion.
- a fifth aspect of the present invention is the crucible with the degassing holes having a diameter of 1 to 5 mm.
- a sixth aspect of the present invention is the crucible with the connecting hole having a diameter of 1 to 5 mm.
- a seventh aspect of the present invention is the crucible with the area of the degassing holes smaller than the area of the connecting hole.
- An eighth aspect of the present invention is the crucible with the degassing holes point symmetric with respect to the central axis of the crucible.
- a ninth aspect of the present invention is the crucible having a cylindrical shape with the bottom face.
- a tenth aspect of the present invention is the crucible having a 250 mm or more inner diameter.
- An eleventh aspect of the present invention is the crucible having a region for mounting a material.
- a twelfth aspect of the present invention is a multi-stage crucible having a region obtained by superimposing a plurality of the crucibles to be used as the region for mounting a material, and having a crucible without a connecting hole at the lowermost stage.
- a thirteenth aspect of the present invention is a crystal production method for producing a calcium fluoride crystal using the crucible.
- a fourteenth aspect of the present invention is a crystal production apparatus having the crucible.
- a fifteenth aspect of the present invention is a crystal production apparatus having the multi-stage crucible.
- a sixteenth aspect of the present invention is a crucible having a plurality of the crucibles superimposed in multi-stages via a gap for a gas passage.
- FIG. 1 is a schematic cross-sectional view showing an embodiment of a crucible to be used in a refining furnace of a production apparatus of a fluoride crystal of the present invention.
- FIG. 2 is a schematic cross-sectional view showing an embodiment of a refining furnace preferably used in the present invention.
- FIG. 3 is a schematic cross-sectional view showing an embodiment of a crystal growth furnace preferably used in the present invention.
- FIG. 4 is a schematic cross-sectional view showing an embodiment of a growth furnace crucible preferably used in the present invention.
- FIG. 5 is a schematic cross-sectional view showing an embodiment of an annealing furnace preferably used in the present invention.
- FIG. 6 is a flow chart of a crystal production process preferably used in the present invention.
- FIG. 7 shows a spectral transmissivity of a fluorite.
- FIG. 8 is a schematic diagram of an exposing device applied with optical parts of the present invention.
- FIG. 9 is a projection optical system of an exposing device applied with optical parts of the present invention.
- FIG. 10 is a schematic diagram of an excimer laser oscillator applied with optical parts of the present invention.
- FIG. 11 is a schematic diagram showing a conventional fluorite production process.
- FIG. 2 shows a refining furnace of a large aperture (aperture 250 mm or more) production apparatus of a fluoride crystal of the present invention.
- a crucible thereof is shown in FIG. 1 in detail.
- the present invention is not limited to the production of a fluoride crystal with a 250 mm or more aperture. Further, the present invention is also preferable for the production of an extremely large aperture fluoride of about 500 mm aperture.
- numeral 201 represents a chamber of the refining furnace, which is connected to a vacuum exhaust system.
- Numeral 202 represents an insulating material, 203 a heater, and 204 a crucible, respectively.
- the crucible for a refining furnace of the present invention is divided in a plurality, and superimposed in multi-stages.
- Numeral 100 represents a crucible main body, and 101 a lid for preventing evaporation of a material, respectively.
- the number of stages shown in an embodiment in FIG. 1 is three, it can be two or four or more.
- the entire surface of the crucible main body 100 and the lid 101 has minute unevenness so that even when the lid 101 covers the crucible main body 100 , the inside of the crucible main body 100 is not closed completely. Further, similarly, the adjacent crucibles have a minute gap allowing the gas passage formed therebetween.
- the size of the crucibles of each stage to be used in the present invention depends on the size of the fluoride crystal to be obtained. For example, since a crystal with about 250 mm to 500 mm aperture and about 10 mm to 100 mm thickness is needed in the case of a lens for an exposing device, a crucible with about 250 mm to 550 mm inner diameter and about 30 mm to 300 mm inner height is preferable. When a thin crystal is needed, the inner height can be 10 mm to 50 mm. When a crystal with a further smaller aperture is needed, the inner diameter can be smaller than 250 mm, for example, 80 mm to 100 mm.
- the inner height of the crucible of each stage can be determined further preferably according to the state of the material such that the height of the molten material becomes 50 mm or less.
- the crucible shown in FIG. 1B has degassing holes 102 on the crucible side face in each stage.
- An impurity gas such as a scavenger can be discharged from the gap between the crucibles or the crucible and the lid in the configuration of FIG. 1A.
- the gas can be discharged mainly from the degassing holes 102 .
- the size of the degassing holes 102 is preferably 1 to 5 mm ⁇ . And it is preferable to provide the degassing holes symmetrically on the crucible side wall.
- fluoride materials fluorite ores and synthetic fluoride materials can be used. In the present invention, the latter can be used preferably.
- a calcium fluoride material and a scavenger are mixed. At the time, it is preferable to mix by placing the calcium fluoride material and the scavenger in a container and rotating the container.
- scavengers include cadmium fluoride, lead fluoride, zinc fluoride, bismuth fluoride, sodium fluoride, and lithium fluoride.
- the scavenger those which can bond with oxygen easily compared with a fluoride to be grown, can be eliminated by the reaction with an oxide contained in the synthetic fluoride material, can provide a high purity, and cannot influence optical characteristics even when a minute amount thereof remains, are selected.
- zinc fluoride and bismuth fluoride are particularly preferable.
- the amount of a scavenger is preferably from 0.04 mol % to 5 mol %, more preferably from 0.1 to 1 mol %.
- the range is advantageous in that generated ZnO, and the like can be eliminated in a high temperature condition in each process, and that even when a minute amount thereof remains, optical characteristics can hardly be influenced.
- the mixed fluoride material is placed in a multi-stage crucible having a desired size in each stage, melted, and crystallized.
- the melting temperature can be a melting point of the fluoride or higher. Preferably it is 1390 to 1450° C.
- thermocouple made from platinum (not illustrated) was used for measuring the temperature.
- the crucible temperature was measured with the thermocouple in the vicinity of the outer wall of the crucible.
- the measured temperature in the range from 1380 to 1450° C. was preferable.
- Crystallization is conducted by gradually cooling the molten fluoride.
- the fluoride to be obtained in this stage is not necessarily single crystalline but can be polycrystalline.
- the surface layer of the obtained fluoride crystal is eliminated by 1 to 2 mm. It is also possible to conduct crystallization by cooling while lowering the crucible. In this case, the impurities can be eliminated further effectively.
- a refined fluoride crystal is placed in a growth furnace crucible having a diameter larger than the refining crucible alone or in a plurality in a superimposed state. It is preferable that the size (diameter) of the fluoride crystal obtained in the refining furnace crucible is 0.9 to 0.95 times as large as the size (diameter) of the growth furnace crucible. That is, it is preferable that the ratio of the size (diameter) of the fluoride obtained in the refining furnace and the size (diameter) of the growth furnace crucible is 1:1.05 to 1:1.1. As mentioned above, since the crucible surface has minute unevenness, the fluoride crystal can be taken out easily from the refining furnace crucible. Further, the taken-out fluoride crystal can be placed in the growth furnace crucible without pulverization.
- FIG. 3 is a schematic diagram showing a growth furnace to be used in the crystal growth process.
- numeral 301 represents a chamber for the growth furnace, 302 an insulating material, 303 a heater, 304 a crucible, 305 a fluoride and 306 a crucible lowering mechanism.
- the growth furnace crucible is a multi-stage crucible like the refining furnace crucible as shown in FIG. 4 since the impurities in a material and a scavenger reaction product can be eliminated efficiently so that impurities in the crystal to be finally obtained can be further restrained, a crystal with a high transmissivity can be obtained.
- FIG. 4A shows a multi-stage crucible with the simplest configuration of the present invention.
- the internal height of the crucible in each stage it is preferable to determine the internal height of the crucible in each stage according to the state of the material such that the height of the crystal block to be produced becomes 10 mm to 50 mm. Since the height of the crystal block becomes the internal height of the crucible in the configuration of FIGS. 4B or 4 C having connecting holes 402 , it is preferable that the internal height of the crucible is 10 mm to 50 mm. With the height of not more than 50 mm, impurities which tends to remain inside a crystal, such as a metal element of a scavenger or oxygen can be discharged efficiently to the outside so that the impurity concentration in the crystal can be further lowered.
- a crystal with a further lower defect density can be obtained. That is, according to the defect evaluation by the etch pit density of a cleavage plane, defect is conspicuous in the vicinity of the crystal bottom face. In order to reduce the influence, it is preferable to have the height of 10 mm or more.
- the internal height of the crucible the same as the thickness of the optical part to be produced, a subsequent cutting process can be eliminated to improve the productivity.
- the crucible internal height of each stage is not necessarily the same, but crucibles with different internal heights can be superimposed.
- the crucible shown in FIG. 4B has a connecting hole 402 at the center part of the crucible bottom face in each stage. Through the hole, a molten liquid drops to the lower stage at the time of melting a material so that the stages communicate with each other.
- the size of the connecting holes 402 is preferably 1 to 5 mm diameter so that the molten liquid can drop to the lower stage while overcoming the surface tension.
- the crystallization proceeds from the lowermost stage.
- the crystal of the connecting hole 402 serves as the seed to cause the crystal growth in the upper stages subsequently so as to provide a crystal with an excellent crystal quality.
- a gas in the crucible can be discharged to the outside from the superimposing portions 404 of each stage.
- a material not wettable by a molten liquid such as black lead for the crucible
- leakage of the molten liquid from the superimposing portions 404 can be prevented.
- the configuration of FIG. 4C is further provided with degassing holes 403 in the vicinity of the bottom face.
- degassing holes 403 By the degassing holes 403 , an impurity gas can be discharged further easily so that a crystal with a higher purity can be obtained.
- the size of the degassing holes 403 is preferably smaller than the diameter of the above-mentioned connecting holes 402 , and it is preferable to provide the degassing holes 403 symmetrically.
- the crucible After heating the crucible to about 1390 to 1450° C. so as to melt the fluoride, the crucible is lowered at the rate of about 0.1 to 5.0 mm/h. Even though the crucible is not actively cooled, the temperature of a part of the fluoride is lowered according to the lowering movement of the crucible so as to be crystallized.
- the fluoride crystal after the crystal growth is applied with a heat treatment.
- the crucible is heated to 900 to 1000° C.
- the heating time is preferably 20 hours or more.
- FIG. 5 is a schematic diagram showing an annealing furnace to be used in the annealing process.
- numeral 501 represents a chamber of an annealing furnace, 502 an insulating material, 503 a heater, 504 a crucible and 505 a fluoride crystal.
- the obtained product will be shaped according to an optical material to be provided (convex lens, concave lens, disk shape, plate shape, and the like).
- a reflection preventing film can be provided on the surface of the optical material of the fluoride crystal.
- the reflection preventing film magnesium fluoride, aluminum oxide, and tantalum oxide can be used preferably. These can be formed by deposition with the resistance heating, electron beam deposition, or sputtering. Since an optical material obtained by the present invention hardly contains water, the reflection preventing film can be attached with an excellent adherence.
- an optical system appropriate for an excimer laser in particular, an ArF excimer laser can be provided.
- an exposing device can be provided by combining an excimer laser light source, an optical system having a lens made from calcium fluoride and a stage capable of moving a substrate.
- Examples of exposing devices include a reduction projection exposing device and a lens type equivalent magnification projection exposing device.
- a stepper applied with a step and repeat method where after exposing one small section (field) of the wafer, an adjacent one field is exposed by moving the wafer by one step, is preferable.
- a stepper applied with a step and repeat method where after exposing one small section (field) of the wafer, an adjacent one field is exposed by moving the wafer by one step.
- it can be preferably used in an exposing device with a micro scan method.
- FIG. 8 shows a schematic configuration of an exposing device of the present invention.
- numeral 21 represents a illumination light source portion and 22 an exposing mechanism portion, which are provided independently. That is, they are physically separated.
- Numeral 23 represents an illumination light source, such as a high output large light source like an excimer laser.
- Numeral 24 represents a mirror, 25 a concave lens, and 26 a convex lens, respectively. 25 and 26 also serve as a beam expander for expanding the beam diameter of a laser to about a size of an optical integrator.
- Numeral 27 represents a mirror, and 28 an optical integrator for evenly illuminating on a reticle.
- the illumination light source portion 21 comprises from the laser 23 to the optical integrator 28 .
- Numeral 29 represents a mirror and 30 a condenser lens for collimating a light flux outputted from the optical integrator.
- Numeral 31 represents a reticle with a circuit pattern formed whereon, 31 a a reticle holder for holding the reticle, 32 a projection optical system for projecting the reticle pattern, and 33 a wafer where the reticle 31 pattern is printed at the projecting lens 32 .
- Numeral 34 represents an XY stage for holding the wafer 33 and moving in the XY directions at the time of printing.
- Numeral 35 represents a fixed table of the exposing device.
- the exposing mechanism portion 22 comprises from the mirror 29 to the fixed table 35 , which are a part of the illumination optical system.
- Numeral 36 represents an alignment means to be used for the TTL alignment.
- an exposing device further comprises an auto focus mechanism, a wafer conveyance mechanism, and the like. These are also included in the exposing mechanism portion 22 .
- FIG. 9 shows an example of an optical material to be used in an exposing device of the present invention, which can be used in the projection optical system of the exposing device shown in FIG. 8.
- the lens assembly comprises 11 lenses L 1 to L 11 without bonding to each other.
- An optical material made of a fluorite of the present invention can be used as a lens or a mirror shown in FIGS. 9 or 10 , or a mirror or a lens of a mirror type exposing device (not illustrated). It is more preferable to provide a reflection preventing film or an amplifying reflection film on the surface of a lens or a mirror.
- an optical part made from a fluoride crystal of the present invention can be used as a prism or an etalon.
- FIGS. 10A and 10B are schematic diagrams of a configuration of an excimer laser oscillator using an optical part made of a fluoride crystal of the present invention.
- the excimer laser oscillator shown in FIG. 10A comprises a resonator 83 for emitting and resonating an excimer laser, an hole 82 for adjusting the excimer laser outputted from the resonator 83 , a prism 84 for having narrowing the band width of the excimer laser light, and a reflecting mirror 81 for reflecting the excimer laser.
- the excimer laser oscillator shown in FIG. 10B comprises a resonator 83 for emitting and resonating an excimer laser, an hole 82 for adjusting the excimer laser outputted from the resonator 83 , an etalon for having the wavelength of the excimer laser to be single, and a reflection mirror for reflecting the excimer laser.
- An excimer laser beam oscillator comprising a fluoride crystal of the present invention as a prism or a etalon can have a further smaller excimer laser wavelength via the prism or the etalon, in other words, can have the wavelength of the excimer laser to be single.
- a powdery calcium fluoride material was placed in a container. 0.08 mol % of a scavenger (ZnF 2 ) was measured based on the material, and added to the container with the material. The container used has a capacity about double as much as the volume of the material. The material and the scavenger were mixed by rotating the container for about 1 hour.
- ZnF 2 a scavenger
- the crucible was set in the refining furnace. By vacuum-exhausting the inside of the chamber 201 , the moisture in the material 205 was eliminated.
- the crucible 204 was heated by the heater 203 .
- the material was melted at 1390 to 1450° C.
- the material filled in the crucible was completely melted.
- the crucible was cooled down by turning off the power of the heater to about the room temperature.
- the fluoride crystals were taken out from each stage and the surface layer thereof was eliminated by about 1 mm.
- ZnF 2 was placed in the crucible 304 as the scavenger. Further, a plurality of the refined crystal blocks were placed in each crucible stage in a superimposed-stage. Then, the crucible was set in the growth furnace. The amount of the ZnF 2 scavenger was 0.02 mol % with respect to the refined crystal blocks.
- the inside of the chamber 301 was vacuum-exhausted to eliminate the moisture in the crystals 305 . Then the crucible was heated by the heater 303 while maintaining the vacuum degree at 5 ⁇ 10 ⁇ 4 Torr or less until the temperature where the material starts melting. The material was melted at 1390 to 1450° C. The material filled in the crucible was completely melted.
- the crucible After reaching the melting temperature, the crucible was maintained until the vacuum degree becomes 2 ⁇ 10 ⁇ 6 Torr or less. Further, the crucible was maintained for about 10 hours after the temperature reaches a stable state.
- the crucible was moved downward by the lowering mechanism 306 at about 2 mm/hour rate.
- the voltage applied to the heater 303 was gradually reduced such that the temperature lowering rate becomes within about 100° C./hour.
- the calcium fluoride crystal was heat-treated.
- the taken-out crystal was set in the annealing crucible 504 .
- About 0.04 mol % of ZnF 2 with respect to the crystal was sprinkled substantially evenly as the scavenger between the crystal and the crucible.
- the inside of the chamber 501 was vacuum-exhausted and gradually heated.
- the temperature schedule was as mentioned below. Room temperature ⁇ 900° C. (rising rate+100° C./h) Maintain at 900° C. (20 hours)
- a fluoride crystal was produced in the process the same as Example 1 except that the crucible shown in FIG. 1B was used instead of the crucible of the refining furnace of Example 1.
- the degassing holes with a 3 mm diameter were provided at 8 positions symmetrically.
- a fluoride crystal was produced in the process the same as Example 1 except that the multi-stage crucible with the configuration of FIG. 4B was used as the growth furnace crucible.
- a fluoride crystal was produced in the process the same as Example 2 except that a crucible having substantially the same configuration as the crucible shown in FIG. 4B was used.
- Example 1 As apparent from the comparison between Example 1 and Conventional Example, by using a multi-stage crucible having a gap to allow the passage of a gas between crucibles for the refining furnace, the transmissivity of the crystal to be finally obtained becomes higher in the short wavelength region. It was also learned that the spectral transmissivity can be further improved in Example 2 where degassing holes are provided in the crucible side face for the refining furnace.
- the refined crystal can be placed in the growth furnace as it is, the productivity can be improved so that an optical material can be produced at a low cost.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
An object of the present invention is to provide a production apparatus and method of a fluoride crystal, and a crucible for the growth capable of efficiently eliminating impurities and a scavenger remained in the crystal so as to produce a fluoride crystal with a high transmissivity. A crucible divided into a plurality to have multi-stages is used for refining a material in the material refining process by adding a scavenger in the material. Further, a degassing hole was provided to the side wall portion of the crucible. A crucible of the present invention has at least two degassing holes at the side wall portion. Further, a crucible of the present invention has a connecting hole at the center part of the bottom face with at least two degassing holes in the side wall portion.
Description
- 1. Field of the Invention
- The present invention relates to a production apparatus of a fluoride crystal preferable for various kinds of optical elements, lens, window materials, prisms, and the like to be used in a wide wavelength range from a vacuum ultraviolet region to a far infrared region, in particular, to a production apparatus of a fluoride crystal to be used for an optical material such as a large aperture lens (aperture of 250 mm or more) for an excimer laser.
- 2.Description of the Related Art
- An excimer laser attracts attention as the only one high output laser to oscillate outside an ultraviolet region so that the application thereof is expected in the electronic industry, chemical industry, and energy industry.
- Specifically, the excimer laser is used in processing metal, resin, glass, ceramics and semiconductors, and a chemical reaction.
- An apparatus for generating an excimer laser beam is known as an excimer laser oscillating apparatus. A laser gas filled in a chamber, such as Ar, Kr, Xe, F 2, Cl2 is excited by the electron beam radiation or the electric discharge. The excited atoms bond with atoms in the ground state so as to produce molecules capable of existing only in the excited state. The molecules are. the excimer. Due to its instability, the excimer immediately discharges the ultraviolet ray and falls into the ground state. This phenomenon is called the bond free transition. An apparatus for taking out a laser beam by amplifying the ultraviolet ray obtained by the transition in an optical resonator comprising a pair of mirrors is an excimer oscillating apparatus.
- Among excimer laser beams, a KrF laser and an Arf laser have a wavelength of 248 nm and 193 nm, respectively in a vacuum ultraviolet ray region so that an optical system having a high transmissivity with respect to the wavelength region needs to be used. Examples of glass materials preferably used in the optical system include fluorides, such as calcium fluoride, magnesium fluoride, barium fluoride, neodymium fluoride, lithium fluoride, and lanthanum fluoride.
- Hereinafter a conventional production method of a fluoride crystal will be explained with reference to an example of calcium fluoride called fluorite, which can be represented by the stoichiometry ratio of CaF 2.
- As conventional production methods of a fluoride crystal, methods disclosed in the official gazettes of Japanese Patent Laid-Open Nos. 4-349199 and 4-349198 can be presented. In short, in order to prevent the loss of weight in directly melting a high purity powdery material produced by a chemical synthesis due to the bulk specific gravity, the high purity material in a cullet state is used at the time of placing the same in a crystal growth furnace. Hereinafter the knowledge obtained by the present inventor to lead to the present invention will be described.
- FIG. 11 is a schematic diagram showing the production method of a fluoride crystal initially conducted by the present inventor.
- In the process S 1, a powdery material is prepared. In the process S2, the material placed in a container is melted, and then cooled. In the process S3, solidified agglomerates are pulverized with a stainless steel pulverizer. In the post process S4, a fluorite block is produced by melting and gradually cooling the pulverized agglomerates placed in a crucible for the crystal growth.
- The process S 2 is conducted for reducing the bulk specific density change before and after melting in the process S4, and further, for eliminating impurities in the material.
- In the processes S 2 and S4, a scavenger, which is a fluoride of a metal, is added in order to eliminate CaO produced by the reaction between the material (CaF2) and water, and the like, or impurities originally existing in the material. For example, a ZnF2 scavenger reacts with CaO so as to be ZnO and eliminated at the time of melting the crystals. As a result, the CaO impurities are eliminated so that a fluoride crystal having an excellent transmissivity characteristic can be obtained.
- The fluoride crystal block accordingly obtained is cut in a desired thickness, processed and shaped to be a desired lens shape to be used as an optical material.
- In the discussion of the production conditions for obtaining a fluoride crystal having a further high transmissivity by the present inventor, it was learned that the crucible structure cast a great influence on the optical characteristics of the crystal after growth.
- That is, in the study on the relationship between the conventional crucible structure to be used in the refining process and the transmissivity of the crystal to be finally obtained, it was learned that although the amount is slight, impurities in a material and a reaction product of a scavenger cannot be discharged to the outside but remain inside the crucible according to the crucible shape. The impurities deteriorate the optical characteristics of the final crystal, and generate the irregularity among the optical parts.
- In the crystal growth process, a refined block needs to be pulverized and placed in a crucible. However, since the bulk density is lowered by the pulverization, a larger crucible is required for obtaining a desired crystal. Furthermore, due to the necessity of the pulverizing process, the productivity becomes poor. Moreover, a problem is involved in that a minute amount of impurities included at the time of the pulverization deteriorates the transmissivity of the crystal.
- The present invention has been completed based on the knowledge and elaborate study for the solution of the problems. An object of the present invention is to provide a production apparatus of a fluoride crystal capable of producing a fluoride crystal having a high transmissivity, and efficiently eliminating impurities and a scavenger remained in the crystal.
- Another object of the present invention is to provide a production apparatus of a fluoride crystal with a high productivity.
- In order to solve the above-mentioned problems, the below-mentioned inventions are provided.
- A first aspect of the present invention is a production apparatus of a fluoride crystal having a crucible divided in a plurality to have multi-stages, to be used for refining a material in a process for refining the material by adding a scavenger in the material.
- A second aspect of the present invention is the production apparatus of a fluoride crystal having a degassing hole on a side wall portion of the crucible.
- A third aspect of the present invention is a crucible having at least two degassing holes on a side wall portion.
- A fourth aspect of the present invention is the crucible having a connecting hole in the bottom center portion, and having at least two degassing holes on a side wall portion.
- A fifth aspect of the present invention is the crucible with the degassing holes having a diameter of 1 to 5 mm.
- A sixth aspect of the present invention is the crucible with the connecting hole having a diameter of 1 to 5 mm.
- A seventh aspect of the present invention is the crucible with the area of the degassing holes smaller than the area of the connecting hole.
- An eighth aspect of the present invention is the crucible with the degassing holes point symmetric with respect to the central axis of the crucible.
- A ninth aspect of the present invention is the crucible having a cylindrical shape with the bottom face.
- A tenth aspect of the present invention is the crucible having a 250 mm or more inner diameter.
- An eleventh aspect of the present invention is the crucible having a region for mounting a material.
- A twelfth aspect of the present invention is a multi-stage crucible having a region obtained by superimposing a plurality of the crucibles to be used as the region for mounting a material, and having a crucible without a connecting hole at the lowermost stage.
- A thirteenth aspect of the present invention is a crystal production method for producing a calcium fluoride crystal using the crucible.
- A fourteenth aspect of the present invention is a crystal production apparatus having the crucible.
- A fifteenth aspect of the present invention is a crystal production apparatus having the multi-stage crucible.
- A sixteenth aspect of the present invention is a crucible having a plurality of the crucibles superimposed in multi-stages via a gap for a gas passage.
- FIG. 1 is a schematic cross-sectional view showing an embodiment of a crucible to be used in a refining furnace of a production apparatus of a fluoride crystal of the present invention.
- FIG. 2 is a schematic cross-sectional view showing an embodiment of a refining furnace preferably used in the present invention.
- FIG. 3 is a schematic cross-sectional view showing an embodiment of a crystal growth furnace preferably used in the present invention.
- FIG. 4 is a schematic cross-sectional view showing an embodiment of a growth furnace crucible preferably used in the present invention.
- FIG. 5 is a schematic cross-sectional view showing an embodiment of an annealing furnace preferably used in the present invention.
- FIG. 6 is a flow chart of a crystal production process preferably used in the present invention.
- FIG. 7 shows a spectral transmissivity of a fluorite.
- FIG. 8 is a schematic diagram of an exposing device applied with optical parts of the present invention.
- FIG. 9 is a projection optical system of an exposing device applied with optical parts of the present invention.
- FIG. 10 is a schematic diagram of an excimer laser oscillator applied with optical parts of the present invention.
- FIG. 11 is a schematic diagram showing a conventional fluorite production process.
- FIG. 2 shows a refining furnace of a large aperture (
aperture 250 mm or more) production apparatus of a fluoride crystal of the present invention. A crucible thereof is shown in FIG. 1 in detail. The present invention is not limited to the production of a fluoride crystal with a 250 mm or more aperture. Further, the present invention is also preferable for the production of an extremely large aperture fluoride of about 500 mm aperture. - In FIG. 2, numeral 201 represents a chamber of the refining furnace, which is connected to a vacuum exhaust system.
Numeral 202 represents an insulating material, 203 a heater, and 204 a crucible, respectively. - As shown in FIGS. 1A and 1B, the crucible for a refining furnace of the present invention is divided in a plurality, and superimposed in multi-stages.
Numeral 100 represents a crucible main body, and 101 a lid for preventing evaporation of a material, respectively. Although the number of stages shown in an embodiment in FIG. 1 is three, it can be two or four or more. The entire surface of the cruciblemain body 100 and thelid 101 has minute unevenness so that even when thelid 101 covers the cruciblemain body 100, the inside of the cruciblemain body 100 is not closed completely. Further, similarly, the adjacent crucibles have a minute gap allowing the gas passage formed therebetween. - The size of the crucibles of each stage to be used in the present invention depends on the size of the fluoride crystal to be obtained. For example, since a crystal with about 250 mm to 500 mm aperture and about 10 mm to 100 mm thickness is needed in the case of a lens for an exposing device, a crucible with about 250 mm to 550 mm inner diameter and about 30 mm to 300 mm inner height is preferable. When a thin crystal is needed, the inner height can be 10 mm to 50 mm. When a crystal with a further smaller aperture is needed, the inner diameter can be smaller than 250 mm, for example, 80 mm to 100 mm.
- In the present invention, the inner height of the crucible of each stage can be determined further preferably according to the state of the material such that the height of the molten material becomes 50 mm or less.
- With the height in the molten state of 50 mm or less, impurities which easily remain inside the crystal such as a metal element of a scavenger and oxygen can be efficiently discharged to the outside so that the impurity concentration in the crystal can be further lowered.
- Further, by having multi-stages, crystals with a preferable size can be obtained for the number of the stages at the same time so that the productivity can be improved. By having a size accommodated in a growth furnace crucible in the next process, since it can be placed in the growth furnace as it is so that a pulverization process is not needed, the productivity can be improved.
- The crucible shown in FIG. 1B has degassing
holes 102 on the crucible side face in each stage. An impurity gas such as a scavenger can be discharged from the gap between the crucibles or the crucible and the lid in the configuration of FIG. 1A. With the configuration of FIG. 1B, the gas can be discharged mainly from the degassing holes 102. By providing the degassing holes 102, the discharge of the impurity gas is facilitated so that a crystal of a further higher purity can be obtained. The size of the degassing holes 102 is preferably 1 to 5 mmθ. And it is preferable to provide the degassing holes symmetrically on the crucible side wall. - Hereinafter a production apparatus of the present invention and a production method of a calcium fluoride crystal as a fluoride will be explained.
- (Material Preparation)
- As fluoride materials, fluorite ores and synthetic fluoride materials can be used. In the present invention, the latter can be used preferably.
- (Mixing Process)
- A calcium fluoride material and a scavenger are mixed. At the time, it is preferable to mix by placing the calcium fluoride material and the scavenger in a container and rotating the container. Examples of scavengers include cadmium fluoride, lead fluoride, zinc fluoride, bismuth fluoride, sodium fluoride, and lithium fluoride. As the scavenger, those which can bond with oxygen easily compared with a fluoride to be grown, can be eliminated by the reaction with an oxide contained in the synthetic fluoride material, can provide a high purity, and cannot influence optical characteristics even when a minute amount thereof remains, are selected. Among these examples, zinc fluoride and bismuth fluoride are particularly preferable.
- The amount of a scavenger is preferably from 0.04 mol % to 5 mol %, more preferably from 0.1 to 1 mol %. The range is advantageous in that generated ZnO, and the like can be eliminated in a high temperature condition in each process, and that even when a minute amount thereof remains, optical characteristics can hardly be influenced.
- (Refining Process)
- The mixed fluoride material is placed in a multi-stage crucible having a desired size in each stage, melted, and crystallized.
- The melting temperature can be a melting point of the fluoride or higher. Preferably it is 1390 to 1450° C.
- A thermocouple made from platinum (not illustrated) was used for measuring the temperature. The crucible temperature was measured with the thermocouple in the vicinity of the outer wall of the crucible. By the detailed study of the present inventor, it was learned that the measured temperature in the range from 1380 to 1450° C. was preferable.
- That is, with a temperature lower than 1380° C., the actual temperature in the crucible is low. If the temperature is close to the melting point, it takes a long time to completely melt the material so that the productivity cannot be improved. On the other hand, with a temperature higher than 1450° C., the fluoride material can be evaporated drastically so that the decline of the productivity by the material loss cannot be avoided.
- With the height of a melting liquid in each stage of 50 mm or less, an added scavenger, a reaction product, and the other impurities can be discharged easily.
- Crystallization is conducted by gradually cooling the molten fluoride. The fluoride to be obtained in this stage is not necessarily single crystalline but can be polycrystalline. The surface layer of the obtained fluoride crystal is eliminated by 1 to 2 mm. It is also possible to conduct crystallization by cooling while lowering the crucible. In this case, the impurities can be eliminated further effectively.
- (Crystal Growth Process)
- In the crystal growth process, a refined fluoride crystal is placed in a growth furnace crucible having a diameter larger than the refining crucible alone or in a plurality in a superimposed state. It is preferable that the size (diameter) of the fluoride crystal obtained in the refining furnace crucible is 0.9 to 0.95 times as large as the size (diameter) of the growth furnace crucible. That is, it is preferable that the ratio of the size (diameter) of the fluoride obtained in the refining furnace and the size (diameter) of the growth furnace crucible is 1:1.05 to 1:1.1. As mentioned above, since the crucible surface has minute unevenness, the fluoride crystal can be taken out easily from the refining furnace crucible. Further, the taken-out fluoride crystal can be placed in the growth furnace crucible without pulverization.
- In the crystal growth process, it is preferable to eliminate calcium oxide by adding a scavenger in the growth furnace crucible with the fluoride crystal.
- FIG. 3 is a schematic diagram showing a growth furnace to be used in the crystal growth process. In FIG. 3, numeral 301 represents a chamber for the growth furnace, 302 an insulating material, 303 a heater, 304 a crucible, 305 a fluoride and 306 a crucible lowering mechanism.
- It is preferable that the growth furnace crucible is a multi-stage crucible like the refining furnace crucible as shown in FIG. 4 since the impurities in a material and a scavenger reaction product can be eliminated efficiently so that impurities in the crystal to be finally obtained can be further restrained, a crystal with a high transmissivity can be obtained.
- FIG. 4A shows a multi-stage crucible with the simplest configuration of the present invention.
- In the present invention, it is preferable to determine the internal height of the crucible in each stage according to the state of the material such that the height of the crystal block to be produced becomes 10 mm to 50 mm. Since the height of the crystal block becomes the internal height of the crucible in the configuration of FIGS. 4B or 4C having connecting
holes 402, it is preferable that the internal height of the crucible is 10 mm to 50 mm. With the height of not more than 50 mm, impurities which tends to remain inside a crystal, such as a metal element of a scavenger or oxygen can be discharged efficiently to the outside so that the impurity concentration in the crystal can be further lowered. On the other hand, with the height of not less than 10 mm, a crystal with a further lower defect density can be obtained. That is, according to the defect evaluation by the etch pit density of a cleavage plane, defect is conspicuous in the vicinity of the crystal bottom face. In order to reduce the influence, it is preferable to have the height of 10 mm or more. - Further, with the internal height of the crucible the same as the thickness of the optical part to be produced, a subsequent cutting process can be eliminated to improve the productivity. The crucible internal height of each stage is not necessarily the same, but crucibles with different internal heights can be superimposed.
- The crucible shown in FIG. 4B has a connecting
hole 402 at the center part of the crucible bottom face in each stage. Through the hole, a molten liquid drops to the lower stage at the time of melting a material so that the stages communicate with each other. The size of the connectingholes 402 is preferably 1 to 5 mm diameter so that the molten liquid can drop to the lower stage while overcoming the surface tension. - The crystallization proceeds from the lowermost stage. The crystal of the connecting
hole 402 serves as the seed to cause the crystal growth in the upper stages subsequently so as to provide a crystal with an excellent crystal quality. - A gas in the crucible can be discharged to the outside from the superimposing
portions 404 of each stage. By selecting a material not wettable by a molten liquid such as black lead for the crucible, leakage of the molten liquid from the superimposingportions 404 can be prevented. However, since leakage is liable in the lower stages by the pressure with a large number of crucible stages, it is preferable to have a level difference in the superimposingportions 404 as shown in the figure. - The configuration of FIG. 4C is further provided with degassing
holes 403 in the vicinity of the bottom face. By the degassing holes 403, an impurity gas can be discharged further easily so that a crystal with a higher purity can be obtained. The size of the degassing holes 403 is preferably smaller than the diameter of the above-mentioned connectingholes 402, and it is preferable to provide the degassing holes 403 symmetrically. - After heating the crucible to about 1390 to 1450° C. so as to melt the fluoride, the crucible is lowered at the rate of about 0.1 to 5.0 mm/h. Even though the crucible is not actively cooled, the temperature of a part of the fluoride is lowered according to the lowering movement of the crucible so as to be crystallized.
- (Annealing Process)
- The fluoride crystal after the crystal growth is applied with a heat treatment. In the annealing process, the crucible is heated to 900 to 1000° C. The heating time is preferably 20 hours or more.
- FIG. 5 is a schematic diagram showing an annealing furnace to be used in the annealing process. In FIG. 5, numeral 501 represents a chamber of an annealing furnace, 502 an insulating material, 503 a heater, 504 a crucible and 505 a fluoride crystal.
- (Processing)
- The obtained product will be shaped according to an optical material to be provided (convex lens, concave lens, disk shape, plate shape, and the like). As needed, a reflection preventing film can be provided on the surface of the optical material of the fluoride crystal. As the reflection preventing film, magnesium fluoride, aluminum oxide, and tantalum oxide can be used preferably. These can be formed by deposition with the resistance heating, electron beam deposition, or sputtering. Since an optical material obtained by the present invention hardly contains water, the reflection preventing film can be attached with an excellent adherence.
- By combining various kinds of lenses accordingly obtained, an optical system appropriate for an excimer laser, in particular, an ArF excimer laser can be provided. Furthermore, an exposing device can be provided by combining an excimer laser light source, an optical system having a lens made from calcium fluoride and a stage capable of moving a substrate.
- Hereinafter an exposing device applied with an optical material of the prevent invention will be explained.
- Examples of exposing devices include a reduction projection exposing device and a lens type equivalent magnification projection exposing device.
- In particular, in order to expose the entire surface of a wafer, a stepper applied with a step and repeat method, where after exposing one small section (field) of the wafer, an adjacent one field is exposed by moving the wafer by one step, is preferable. Of course it can be preferably used in an exposing device with a micro scan method.
- FIG. 8 shows a schematic configuration of an exposing device of the present invention. In FIG. 8, numeral 21 represents a illumination light source portion and 22 an exposing mechanism portion, which are provided independently. That is, they are physically separated.
Numeral 23 represents an illumination light source, such as a high output large light source like an excimer laser.Numeral 24 represents a mirror, 25 a concave lens, and 26 a convex lens, respectively. 25 and 26 also serve as a beam expander for expanding the beam diameter of a laser to about a size of an optical integrator.Numeral 27 represents a mirror, and 28 an optical integrator for evenly illuminating on a reticle. The illuminationlight source portion 21 comprises from thelaser 23 to theoptical integrator 28.Numeral 29 represents a mirror and 30 a condenser lens for collimating a light flux outputted from the optical integrator.Numeral 31 represents a reticle with a circuit pattern formed whereon, 31 a a reticle holder for holding the reticle, 32 a projection optical system for projecting the reticle pattern, and 33 a wafer where thereticle 31 pattern is printed at the projectinglens 32.Numeral 34 represents an XY stage for holding thewafer 33 and moving in the XY directions at the time of printing.Numeral 35 represents a fixed table of the exposing device. - The exposing
mechanism portion 22 comprises from themirror 29 to the fixed table 35, which are a part of the illumination optical system.Numeral 36 represents an alignment means to be used for the TTL alignment. In general, an exposing device further comprises an auto focus mechanism, a wafer conveyance mechanism, and the like. These are also included in the exposingmechanism portion 22. - FIG. 9 shows an example of an optical material to be used in an exposing device of the present invention, which can be used in the projection optical system of the exposing device shown in FIG. 8. The lens assembly comprises 11 lenses L1 to L11 without bonding to each other. An optical material made of a fluorite of the present invention can be used as a lens or a mirror shown in FIGS. 9 or 10, or a mirror or a lens of a mirror type exposing device (not illustrated). It is more preferable to provide a reflection preventing film or an amplifying reflection film on the surface of a lens or a mirror.
- Furthermore, an optical part made from a fluoride crystal of the present invention can be used as a prism or an etalon.
- FIGS. 10A and 10B are schematic diagrams of a configuration of an excimer laser oscillator using an optical part made of a fluoride crystal of the present invention.
- The excimer laser oscillator shown in FIG. 10A comprises a
resonator 83 for emitting and resonating an excimer laser, anhole 82 for adjusting the excimer laser outputted from theresonator 83, aprism 84 for having narrowing the band width of the excimer laser light, and a reflectingmirror 81 for reflecting the excimer laser. - The excimer laser oscillator shown in FIG. 10B comprises a
resonator 83 for emitting and resonating an excimer laser, anhole 82 for adjusting the excimer laser outputted from theresonator 83, an etalon for having the wavelength of the excimer laser to be single, and a reflection mirror for reflecting the excimer laser. - An excimer laser beam oscillator comprising a fluoride crystal of the present invention as a prism or a etalon can have a further smaller excimer laser wavelength via the prism or the etalon, in other words, can have the wavelength of the excimer laser to be single.
- By radiating an excimer laser beam to a photosensitized resist on a substrate via a reticle pattern with the exposing device, a latent image corresponding to the pattern to be formed can be provided.
- A production apparatus of a fluoride crystal of the present invention will be explained concretely with reference to examples.
- In this example, a calcium fluoride crystal was produced according to a procedure shown in FIG. 6. Hereinafter each process will be explained.
- (Prescription, Mixing Process)
- A powdery calcium fluoride material was placed in a container. 0.08 mol % of a scavenger (ZnF 2) was measured based on the material, and added to the container with the material. The container used has a capacity about double as much as the volume of the material. The material and the scavenger were mixed by rotating the container for about 1 hour.
- (Refining Process)
- The material was refined with a refining furnace shown in FIG. 2.
- A multi-stage crucible shown in FIG. 1A with three stages was used.
- After filling the prepared material in each stage of the crucible, the crucible was set in the refining furnace. By vacuum-exhausting the inside of the
chamber 201, the moisture in the material 205 was eliminated. - While maintaining the vacuum degree at 5×10 −4 Torr or less until the temperature where the material starts melting, the
crucible 204 was heated by theheater 203. The material was melted at 1390 to 1450° C. The material filled in the crucible was completely melted. - After reaching the melting temperature, the crucible was maintained until the vacuum degree becomes 2×10 −6 Torr or less.
- Then, the crucible was cooled down by turning off the power of the heater to about the room temperature. The fluoride crystals were taken out from each stage and the surface layer thereof was eliminated by about 1 mm.
- (Crystal Growth Process)
- Then the crystal growth of the calcium fluoride was conducted with the growth furnace shown in FIG. 3.
- ZnF 2 was placed in the
crucible 304 as the scavenger. Further, a plurality of the refined crystal blocks were placed in each crucible stage in a superimposed-stage. Then, the crucible was set in the growth furnace. The amount of the ZnF2 scavenger was 0.02 mol % with respect to the refined crystal blocks. - The inside of the
chamber 301 was vacuum-exhausted to eliminate the moisture in thecrystals 305. Then the crucible was heated by theheater 303 while maintaining the vacuum degree at 5×10−4 Torr or less until the temperature where the material starts melting. The material was melted at 1390 to 1450° C. The material filled in the crucible was completely melted. - After reaching the melting temperature, the crucible was maintained until the vacuum degree becomes 2×10 −6 Torr or less. Further, the crucible was maintained for about 10 hours after the temperature reaches a stable state.
- The crucible was moved downward by the lowering mechanism 306 at about 2 mm/hour rate. When the crucible was completely lowered, the voltage applied to the
heater 303 was gradually reduced such that the temperature lowering rate becomes within about 100° C./hour. - The power of the heater was switched off to cool down to about the room temperature. The calcium fluoride crystal (50 mm thickness) was taken out from the furnace.
- (Annealing Process)
- With the annealing furnace shown in FIG. 5, the calcium fluoride crystal was heat-treated. The taken-out crystal was set in the
annealing crucible 504. About 0.04 mol % of ZnF2 with respect to the crystal was sprinkled substantially evenly as the scavenger between the crystal and the crucible. The inside of thechamber 501 was vacuum-exhausted and gradually heated. The temperature schedule was as mentioned below. Room temperature→900° C. (rising rate+100° C./h) Maintain at 900° C. (20 hours) - 900° C→room temperature (lowering rate —6° C./h)
- After cooling to about the room temperature, the crystal was taken out from the furnace.
- The crystal accordingly produced was cut in a 10 mm thickness and abraded.
- In this embodiment, a fluoride crystal was produced in the process the same as Example 1 except that the crucible shown in FIG. 1B was used instead of the crucible of the refining furnace of Example 1. The degassing holes with a 3 mm diameter were provided at 8 positions symmetrically.
- In this embodiment, a fluoride crystal was produced in the process the same as Example 1 except that the multi-stage crucible with the configuration of FIG. 4B was used as the growth furnace crucible.
- In this embodiment, a fluoride crystal was produced in the process the same as Example 2 except that a crucible having substantially the same configuration as the crucible shown in FIG. 4B was used.
- In order to evaluate the performances of the fluoride crystals obtained in Examples 1 to 4, a calcium fluoride crystal was produced as the comparative example in the process the same as Example 1 except that a block produced in the conventional production process explained with reference to FIG. 11 excluding the process for eliminating an impurity gas was pulverized and used as the material.
- The spectral transmissivity of the fluorites produced in Examples 1 to 4 and Conventional Example are shown in FIG. 7.
- As apparent from the comparison between Example 1 and Conventional Example, by using a multi-stage crucible having a gap to allow the passage of a gas between crucibles for the refining furnace, the transmissivity of the crystal to be finally obtained becomes higher in the short wavelength region. It was also learned that the spectral transmissivity can be further improved in Example 2 where degassing holes are provided in the crucible side face for the refining furnace.
- Furthermore, it was learned that the spectral transmissivity can be further higher in Examples 3 and 4 with a multi-stage crucible for the growth furnace compared with the corresponding Examples 1 and 2.
- As mentioned above, according to the present invention, since a scavenger and the other impurity gases can be eliminated efficiently from the crystal, a fluoride crystal with a high transmissivity can be obtained.
- Accordingly, even when a short wavelength light beam of a high output is radiated repeatedly over a long period, a highly reliable fluoride crystal without the risk of deteriorating the transmissivity characteristics can be provided.
- Furthermore, according to the present invention, since the refined crystal can be placed in the growth furnace as it is, the productivity can be improved so that an optical material can be produced at a low cost.
Claims (16)
1. A production apparatus of a fluoride crystal having a crucible divided in a plurality to have multi-stages, to be used for refining a material in a process for refining the material by adding a scavenger in the material.
2. The production apparatus of a fluoride crystal according to claim 1 , wherein a degassing hole is provided on a side wall portion of the crucible.
3. A crucible having at least two degassing holes on a side wall portion.
4. A crucible having a connecting hole in the bottom center portion, and at least two degassing holes on a side wall portion.
5. The crucible according to claim 3 or 4, wherein the degassing holes have a diameter of 1 to 5 mm.
6. The crucible according to claim 4 or 5, wherein the connecting hole has a diameter of 1 to 5 mm.
7. The crucible according to any of claims 4 to 6 , wherein the area of the degassing holes is smaller than the area of the connecting hole.
8. The crucible according to any of claims 3 to 7 , wherein the degassing holes are point symmetric with respect to the central axis of the crucible.
9. The crucible according to any of claims 3 to 8 , having a cylindrical shape with the bottom face.
10. The crucible according to any of claims 3 to 9 , having a 250 mm or more inner diameter.
11. The crucible according to any of claims 3 to 10 , having a region for mounting a material.
12. A multi-stage crucible having a region obtained by superimposing a plurality of the crucibles according to claim 3 or 4 as the region for mounting a material, and having a crucible without a connecting hole at the lowermost stage.
13. A crystal production method for producing a calcium fluoride crystal using the crucible according to claim 11 or 12.
14. A crystal production apparatus having the crucible according to any of claims 3 to 11 .
15. A crystal production apparatus having the multi-stage crucible according to claim 12 .
16. A crucible having a plurality of the crucibles superimposed in multi-stages via a gap for a gas passage.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/715,453 US20040123795A1 (en) | 1997-03-31 | 2003-11-19 | Production apparatus and method of fluoride crystal, and crucible |
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8162497 | 1997-03-31 | ||
| JP081624/1997 | 1997-03-31 | ||
| JP063952/1998 | 1998-02-27 | ||
| JP06395298A JP3475407B2 (en) | 1997-03-31 | 1998-02-27 | Apparatus and method for producing fluoride crystal and crucible |
| US09/048,795 US6875275B1 (en) | 1997-03-31 | 1998-03-27 | Production apparatus for producing a crystal |
| US10/715,453 US20040123795A1 (en) | 1997-03-31 | 2003-11-19 | Production apparatus and method of fluoride crystal, and crucible |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/048,795 Division US6875275B1 (en) | 1997-03-31 | 1998-03-27 | Production apparatus for producing a crystal |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20040123795A1 true US20040123795A1 (en) | 2004-07-01 |
Family
ID=26405080
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/048,795 Expired - Fee Related US6875275B1 (en) | 1997-03-31 | 1998-03-27 | Production apparatus for producing a crystal |
| US10/715,453 Abandoned US20040123795A1 (en) | 1997-03-31 | 2003-11-19 | Production apparatus and method of fluoride crystal, and crucible |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/048,795 Expired - Fee Related US6875275B1 (en) | 1997-03-31 | 1998-03-27 | Production apparatus for producing a crystal |
Country Status (2)
| Country | Link |
|---|---|
| US (2) | US6875275B1 (en) |
| JP (1) | JP3475407B2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6929694B2 (en) | 2002-02-19 | 2005-08-16 | Canon Kabushiki Kaisha | Crystal manufacture method |
| CN104131337A (en) * | 2014-07-17 | 2014-11-05 | 大连理工大学 | Crucible with impurity removal function and polysilicon purification or ingot method used in polysilicon purification or ingot casting |
| EP3587628A1 (en) * | 2018-06-29 | 2020-01-01 | Hanergy New Material Technology Co., Ltd. | Reaction device for horizontal boat production method |
| US12516445B2 (en) | 2021-02-01 | 2026-01-06 | Sm Lab Co., Ltd. | Crucible and crucible assembly, for preparing cathode active material |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3475407B2 (en) * | 1997-03-31 | 2003-12-08 | キヤノン株式会社 | Apparatus and method for producing fluoride crystal and crucible |
| US6289187B1 (en) * | 1999-02-04 | 2001-09-11 | Xerox Corporation | Carbon fiber commutator brush for a toner developing device and method for making |
| EP1154046B1 (en) * | 2000-05-09 | 2011-12-28 | Hellma Materials GmbH & Co. KG | Fluoride crystalline optical lithography lens element blank |
| WO2002031232A1 (en) | 2000-10-13 | 2002-04-18 | Corning Incorporated | Method and device for producing optical fluoride crystals |
| FR2822853B1 (en) * | 2001-03-29 | 2003-06-27 | Corning Inc | PREPARATION OF (MONO) CRYSTALS |
| DE102004003829A1 (en) | 2004-01-26 | 2005-08-18 | Schott Ag | A method for cleaning crystal material and for producing crystals, an apparatus therefor and the use of the crystals thus obtained |
| KR101494531B1 (en) * | 2013-06-27 | 2015-02-17 | 웅진에너지 주식회사 | Crucible for Ingot glower |
| JP6314407B2 (en) * | 2013-10-07 | 2018-04-25 | 宇部興産株式会社 | Method for producing ceramic composite material for light conversion |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2214976A (en) * | 1939-01-05 | 1940-09-17 | Research Corp | Apparatus for the manufacture of crystalline bodies |
| US3981818A (en) * | 1971-10-26 | 1976-09-21 | The Harshaw Chemical Company | Crystalline materials |
| US4030965A (en) * | 1976-06-09 | 1977-06-21 | The Harshaw Chemical Company | Crystal growth procedure |
| US4032313A (en) * | 1973-10-04 | 1977-06-28 | Canon Kabushiki Kaisha | Apparatus for producing optical fibers by using crucibles |
| US4076574A (en) * | 1975-12-29 | 1978-02-28 | Hughes Aircraft Company | Reactive atmosphere crystal growth method |
| US4379733A (en) * | 1981-10-02 | 1983-04-12 | Hughes Aircraft Company | Bicameral mode crystal growth apparatus and process |
| US4649002A (en) * | 1985-04-01 | 1987-03-10 | Kennecott Corporation | System for preventing decomposition of silicon carbide articles during sintering |
| US4818282A (en) * | 1981-11-07 | 1989-04-04 | Leybold-Heraeus Gmbh | Method for recovering metal-carbide scrap by alloying |
| US6270570B2 (en) * | 1997-03-31 | 2001-08-07 | Canon Kabushiki Kaisha | Fluoride crystal, optical article, and production method |
| US6875275B1 (en) * | 1997-03-31 | 2005-04-05 | Canon Kabushiki Kaisha | Production apparatus for producing a crystal |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6144792A (en) | 1984-08-09 | 1986-03-04 | Toshiba Ceramics Co Ltd | Apparatus for pulling up silicon single crystal |
| JP3006147B2 (en) | 1991-05-23 | 2000-02-07 | 株式会社ニコン | Large diameter fluorite single crystal manufacturing equipment |
| JP3006148B2 (en) | 1991-05-23 | 2000-02-07 | 株式会社ニコン | Fluorite production equipment with excellent excimer resistance |
-
1998
- 1998-02-27 JP JP06395298A patent/JP3475407B2/en not_active Expired - Fee Related
- 1998-03-27 US US09/048,795 patent/US6875275B1/en not_active Expired - Fee Related
-
2003
- 2003-11-19 US US10/715,453 patent/US20040123795A1/en not_active Abandoned
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2214976A (en) * | 1939-01-05 | 1940-09-17 | Research Corp | Apparatus for the manufacture of crystalline bodies |
| US3981818A (en) * | 1971-10-26 | 1976-09-21 | The Harshaw Chemical Company | Crystalline materials |
| US4032313A (en) * | 1973-10-04 | 1977-06-28 | Canon Kabushiki Kaisha | Apparatus for producing optical fibers by using crucibles |
| US4076574A (en) * | 1975-12-29 | 1978-02-28 | Hughes Aircraft Company | Reactive atmosphere crystal growth method |
| US4030965A (en) * | 1976-06-09 | 1977-06-21 | The Harshaw Chemical Company | Crystal growth procedure |
| US4379733A (en) * | 1981-10-02 | 1983-04-12 | Hughes Aircraft Company | Bicameral mode crystal growth apparatus and process |
| US4818282A (en) * | 1981-11-07 | 1989-04-04 | Leybold-Heraeus Gmbh | Method for recovering metal-carbide scrap by alloying |
| US4649002A (en) * | 1985-04-01 | 1987-03-10 | Kennecott Corporation | System for preventing decomposition of silicon carbide articles during sintering |
| US6270570B2 (en) * | 1997-03-31 | 2001-08-07 | Canon Kabushiki Kaisha | Fluoride crystal, optical article, and production method |
| US6875275B1 (en) * | 1997-03-31 | 2005-04-05 | Canon Kabushiki Kaisha | Production apparatus for producing a crystal |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6929694B2 (en) | 2002-02-19 | 2005-08-16 | Canon Kabushiki Kaisha | Crystal manufacture method |
| US20050227849A1 (en) * | 2002-02-19 | 2005-10-13 | Kentaro Doguchi | Optical element made of fluoride crystal |
| CN104131337A (en) * | 2014-07-17 | 2014-11-05 | 大连理工大学 | Crucible with impurity removal function and polysilicon purification or ingot method used in polysilicon purification or ingot casting |
| EP3587628A1 (en) * | 2018-06-29 | 2020-01-01 | Hanergy New Material Technology Co., Ltd. | Reaction device for horizontal boat production method |
| US12516445B2 (en) | 2021-02-01 | 2026-01-06 | Sm Lab Co., Ltd. | Crucible and crucible assembly, for preparing cathode active material |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3475407B2 (en) | 2003-12-08 |
| US6875275B1 (en) | 2005-04-05 |
| JPH10330192A (en) | 1998-12-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0869203B1 (en) | Calcium Fluoride crystal, optical article and production method | |
| EP0995820B1 (en) | Fluoride refining method and fluoride crystal manufacturing method, and optical part and aligner using same | |
| EP0939147B1 (en) | A manufacturing method for calcium fluoride and calcium fluoride for photolithography | |
| US6342312B2 (en) | Calcium fluoride crystal, optical article and exposure apparatus for photo-lithography using the same | |
| US6875275B1 (en) | Production apparatus for producing a crystal | |
| US6238479B1 (en) | Raw material for manufacturing fluoride crystal, refining method of the same, fluoride crystal, manufacturing method of the same, and optical part | |
| JP3697008B2 (en) | Fluoride crystal and method for producing fluoride crystal lens | |
| US6878201B2 (en) | Methods of making fluoride crystal and fluoride crystal lens | |
| JP2003342098A (en) | Apparatus and method for producing fluoride crystal | |
| JP3957782B2 (en) | Fluorite, manufacturing method thereof and exposure apparatus | |
| JP2004002196A (en) | Apparatus and method for producing fluoride crystal and crucible | |
| JPH10279396A (en) | Fluoride crystal manufacturing equipment | |
| JPH09315815A (en) | Fluorite, optical article using the same, and exposure apparatus for photolithography | |
| JP3337605B2 (en) | Magnesium-containing fluorite, optical system and exposure apparatus using the same | |
| JP4277595B2 (en) | Fluoride crystal manufacturing method, calcium fluoride crystal and exposure apparatus | |
| JP2003238293A (en) | Fluorite, its production method, optical system and exposure apparatus using fluorite | |
| JPH1160382A (en) | Fluorite single crystal and optical lithography apparatus using the same | |
| JP2002308694A (en) | Method for producing fluoride crystal and fluoride crystal lens | |
| JP2003221297A (en) | Method for producing calcium fluoride crystal | |
| JPH09258001A (en) | Aluminum-containing fluorite, optical system and exposure apparatus using the same | |
| JP2003238292A (en) | Method for producing fluorite crystals | |
| JP2007126353A (en) | Fluorite, optical system and exposure apparatus using the same | |
| JP2000203994A (en) | Fluorite single crystal, heat treatment method thereof, and method for producing fluorite single crystal material | |
| JP2005330123A (en) | Method for producing caf2 crystal | |
| JP2003089591A (en) | Single crystal growth method, floating member for single crystal growth, crystal, optical component, and exposure apparatus |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |