EP0650184A1 - Struktur von abtichtungsteil einer bogenröhre und verfahren zur herstellung derselben - Google Patents

Struktur von abtichtungsteil einer bogenröhre und verfahren zur herstellung derselben Download PDF

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Publication number
EP0650184A1
EP0650184A1 EP93914987A EP93914987A EP0650184A1 EP 0650184 A1 EP0650184 A1 EP 0650184A1 EP 93914987 A EP93914987 A EP 93914987A EP 93914987 A EP93914987 A EP 93914987A EP 0650184 A1 EP0650184 A1 EP 0650184A1
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EP
European Patent Office
Prior art keywords
bulb
core
side region
layer
ingredient
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EP93914987A
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English (en)
French (fr)
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EP0650184A4 (de
EP0650184B1 (de
Inventor
Hiroyuki Toto Ltd Nagayama
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Toto Ltd
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Toto Ltd
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
    • H01J9/24—Manufacture or joining of vessels, leading-in conductors or bases
    • H01J9/26—Sealing together parts of vessels
    • H01J9/265—Sealing together parts of vessels specially adapted for gas-discharge tubes or lamps
    • H01J9/266—Sealing together parts of vessels specially adapted for gas-discharge tubes or lamps specially adapted for gas-discharge lamps
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00—Gas-discharge or vapour-discharge lamps
    • H01J61/02—Details
    • H01J61/30—Vessels; Containers
    • H01J61/302—Vessels; Containers characterised by the material of the vessel
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00—Gas-discharge or vapour-discharge lamps
    • H01J61/02—Details
    • H01J61/36—Seals between parts of vessels; Seals for leading-in conductors; Leading-in conductors
    • H01J61/361—Seals between parts of vessel
    • H01J61/363—End-disc seals or plug seals
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00—Gas-discharge or vapour-discharge lamps
    • H01J61/02—Details
    • H01J61/36—Seals between parts of vessels; Seals for leading-in conductors; Leading-in conductors
    • H01J61/366—Seals for leading-in conductors
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00—Gas-discharge or vapour-discharge lamps
    • H01J61/82—Lamps with high-pressure unconstricted discharge having a cold pressure > 400 Torr

Definitions

  • the present invention relates to a sealing structure for a light-emitting bulb assembly for use in a metal-vapor discharge lamp such as a mercury-vapor lamp, a metal halide lamp, or a sodium-vapor lamp, or a high-intensity discharge lamp, and a method of manufacturing such a light-emitting bulb assembly.
  • a metal-vapor discharge lamp such as a mercury-vapor lamp, a metal halide lamp, or a sodium-vapor lamp, or a high-intensity discharge lamp
  • Metal-vapor discharge lamps include a mercury-vapor lamp, a metal halide lamp, and a sodium-vapor lamp.
  • the mercury-vapor lamp emits light excited from the mercury in a positive column produced in a hot-cathode arc discharge.
  • a metal halide is evaporated into a metal and a halogen by the heat of a mercury hot-cathode arc discharge to emit light in a color inherent in the metal.
  • the sodium-vapor lamp emits light in yellowish orange at a D line (589.0 nm, 589.9 nm) produced by a hot-cathode arc of a sodium vapor.
  • such metal-vapor discharge lamps have been used as illuminating lamps for gymnasiums and factories, light sources for overhead projectors and color liquid crystal projectors, fog lamps for automobiles, and so on.
  • the bulbs of metal-vapor discharge lamps were initially made of quartz glass. However, since the quartz glass has poor fade resistance and a large thermal capacity, the metal-vapor discharge lamps cannot be turned on quickly and the individual bulbs have large dimensional variations. Therefore, it has recently been proposed to make bulbs of light-transmissive ceramic.
  • a light-emitting bulb assembly for a discharge lamp comprises a bulb made of light-transmissive ceramic in the form of fired alumina or the like, and a closure by which an electrode supported by an electrode support is sealed and fixed in the bulb.
  • a glass solder is filled in a gap between end and inner surfaces of the open end of the bulb and a confronting surface of the closure, heating the glass solder to melt same, and then cooling and solidifying the melted glass solder.
  • the closure prefferably has the same coefficient of thermal expansion as and to be as chemically stable against metal vapor and halogen vapor as the bulb or the electrode support.
  • a starting rare gas and a discharging metal component depending on the discharge lamp which incorporates the bulb assembly e.g., mercury if the discharge lamp is a high-pressure mercury vapor lamp, or a metal halide if the discharge lamp is a metal halide lamp, are sealed in the bulb.
  • the bulb assembly is turned on, its temperature momentarily increases from the atmospheric temperature to 900°C at which the bulb assembly remains energized stably. High thermal stresses are developed in the bulb assembly due to such a large thermal change and a change in the internal pressure.
  • a metal halide e.g., T1I3, NaI, or the like
  • a discharging metal component is liberated as ions which erode the bulb assembly.
  • the liberated ions erode the glass solder more quickly because the glass solder has lower erosion resistance than the light-transmissive ceramic and the closure because of its composition.
  • the glass solder is liable to crack also due to the low erosion resistance against the erosion caused by the liberated ions.
  • Japanese laid-open patent publication No. 1-143132 discloses a technique for brazing an insert having a coefficient of thermal expansion similar to that of alumina to a sealed region of an outer circumferential element of alumina which corresponds to a bulb.
  • a closure is composed of a central body and an annular body disposed around the central body, and a bulb is joined in solid phase to the closure (the central body and the annular body).
  • Japanese laid-open patent publication No. 63-308861 particularly proposes specific dimensions and compositions of the central body and the annular body which make up the closure. Specified dimensions are also proposed in Japanese laid-open patent publication No. 62-21306.
  • the disclosed proposals are effective in suppressing a leakage of the discharging metal component from the bulb assembly for thereby keeping reliable light emission and increasing the service life of the lamp.
  • the conventional light-emitting bulb assembly fails to keep sufficiently reliable light emission and have a sufficiently long service life.
  • Specified dimensions of the closure and other parts are not preferable as they pose limitations on the configurations of the light-emitting bulb assembly and also the configurations of the lamp which accommodates the light-emitting bulb assembly.
  • the present invention has been made in order to solve the above problems. It is an object of the present invention to provide a light-emitting bulb assembly which is highly reliable and has a long service life, and particularly a novel sealing structure for such a light-emitting bulb assembly and a simple method of manufacturing such a light-emitting bulb assembly.
  • a sealing structure for a light-emitting bulb assembly includes a closure having a core which serves as an electrode and sealing an open end of a bulb, the closure including a bulb-side region disposed adjacent to the open end of the bulb and made of a compositional ingredient having a coefficient of thermal expansion which is substantially the same as that of the bulb, a core-side region disposed adjacent to the core and made of a compositional ingredient having a coefficient of thermal expansion which is substantially the same as that of the core, and an intermediate region disposed between the bulb-side region and the core-side region and made of a compositional ingredient having compositional proportions adjusted such that a coefficient of thermal expansion thereof varies gradually from the coefficient of thermal expansion of the bulb-side region toward the coefficient of thermal expansion of the core-side region.
  • layers of the closure are progressively thicker from the bulb-side region layer toward the core-side region layer.
  • the bulb should preferably be made of light-transmissive ceramic, particularly highly pure alumina, and the core should preferably be made primarily of tungsten.
  • the closure may be made of a gradient function material.
  • the above sealing structure may be manufactured by a method given below.
  • a method of manufacturing a light-emitting bulb assembly including a closure having a core which serves as an electrode and sealing an open end of a light-transmissive bulb comprises the steps of:
  • the step (b) may comprise the steps of:
  • the step (b) may comprise the steps of producing green sheets respectively from the core ingredient suspension, the at least one intermediate suspension, and the bulb ingredient suspension, and successively winding the green sheets around the core, thereby forming the unfired laminated body.
  • the core comprises a conductive core made of tungsten or the like
  • the closure hermetically joined in solid phase to the opening of the bulb comprises a fired laminated body composed of a core-side region layer, at least one intermediate region layer, and a bulb-side region layer which are successively arranged from the conductive core toward the bulb.
  • the core-side region layer includes at least 50 % by volume of an ingredient of the conductive core
  • the bulb-side region layer includes at least 80 % by volume of an ingredient of light-transmissive ceramic.
  • the intermediate region layer between the core-side region layer and the bulb-side region layer includes light-transmissive ceramic having a volume ratio which is progressively closer to the volume ratio of the light-transmissive ceramic of the bulb-side region in a direction toward the bulb-side region, and also includes the ingredient of the core having a volume ratio which is progressively closer to the volume ratio of the ingredient of the core in the core-side region layer in a direction toward the core-side region layer.
  • a network structure of crystals is formed between common ingredients by firing, thereby integrally joining the ingredients.
  • a firing process for reducing surface energy is applied to the joining of the core and the opening of the bulb to each other. Impurities such as of glass are often added in a small amount in an effort to accelerate the firing process.
  • each of the layers traps the powder of the ingredient of the conductive core, and the ingredient of the light-transmissive ceramic forms a solid solution and is crystallized.
  • Adjacent layers are integrally joined to each other in solid phase as the ingredient of the light-transmissive ceramic in the layers forms a solid solution and is crystallized at the mating surfaces of the layers.
  • the conductive core and the core-side region layer are also integrally joined to each other in solid phase because the ingredient of the light-transmissive ceramic in the core-side region layer is crystallized in contact with the core, forming a glassy substance which fills in its grain boundaries, and also because the ingredient of the conductive core is contained in both the core and the core-side region layer.
  • the bulb-side region layer and the bulb are also integrally joined to each other in solid phase because the ingredient of the light-transmissive ceramic in the bulb-side region layer is crystallized in contact with the bulb, forming a glassy substance which fills in its grain boundaries, and also because the ingredient of the light-transmissive ceramic is contained in both the bulb-side region layer and the bulb.
  • the closure after it has been fired is firmly bonded to the conductive core, making it possible to seal a main electrode. Additionally, the closure after it has been fired makes it possible to hermetically seal the opening of the bulb through the formation of a glass phase in the grain boundaries of the ingredient of the light-transmissive ceramic in the bulb-side region layer and the bulb.
  • the distribution of coefficients of thermal expansion from the conductive core through the core-side region layer, the intermediate region layer, and the bulb-side region layer to the bulb is a gradient distribution ranging from the coefficient of thermal expansion of the conductive core to the coefficient of thermal expansion of the bulb.
  • an unfired core-side region layer, an unfired intermediate region layer, and an unfired bulb-side region layer are successively stacked on a core made of a conductive material, thereby forming an unfired laminated body.
  • the unfired core-side region layer, the unfired intermediate region layer, and the unfired bulb-side region layer which are successively stacked are formed from a core ingredient suspension including a powder of a conductive material ingredient or a core ingredient and a powder of a light-transmissive ceramic ingredient or a bulb ingredient, with at least 50 % by volume of the conductive material ingredient, a bulb ingredient suspension including both powders with at least 80 % by volume of the light-transmissive ceramic ingredient, and a plurality of intermediate suspensions including both powders with the volume ratio of the light-transmissive ceramic ingredient being progressively increased to a value close to 100 % and the volume ratio of the conductive material ingredient being progressively reduced from 100 %.
  • the unfired core-side region layer, the unfired intermediate region layer, and the unfired bulb-side region layer on an outer surface of the core are deposited in a descending order of volume ratios of the conductive material ingredient, thereby forming the unfired laminated body. Thereafter, the unfired laminated body is disposed at the opening of the bulb so as to position the main electrode connected to the core in the bulb, and then fired.
  • the fired closure is of an integral structure achieved by the formation of a solid solution of and crystallization of the light-transmissive ceramic ingredient between adjacent ones of the layers.
  • the fired closure is firmly bonded to the core, making it possible to seal the main electrode, through the formation of a glass phase in the grain boundaries of the light-transmissive ceramic ingredient in the core-side region layer while it is being held in contact with the core, and also through the coexistence of the conductive core ingredient.
  • the fired closure also makes it possible to hermetically seal the opening of the bulb through the formation of a glass phase in the grain boundaries of the light-transmissive ceramic ingredient in the bulb-side region layer and the bulb.
  • the distribution of coefficients of thermal expansion from the core through the core-side region layer, the intermediate region layer, and the bulb-side region layer to the bulb is a gradient distribution ranging from the coefficient of thermal expansion of the core to the coefficient of thermal expansion of the bulb.
  • a light-emitting bulb assembly according to a first embodiment of the present invention comprises a tubular bulb 1F, a closure 2 fixedly mounted in an electrode holding hole 1a defined in a larger-diameter open end of the bulb 1F, a closure 2A fixedly mounted in an electrode holding hole 1b defined in a smaller-diameter open end of the bulb 1F, and a pair of main electrodes 3 disposed in the bulb 1F.
  • the main electrodes 3 are in the form of tungsten coils, respectively, which are supported by respective support shafts 4 of tungsten which extend through the closures 2, 2A.
  • the closures 2, 2A differ from each other only with respect to their diameters, and are produced by a manufacturing process which will be described later on.
  • the end of the bulb 1F with the electrode holding hole 1b has a slender introduction tube 1c for entering a starting rare gas metal and various discharging material amalgams.
  • the slender introduction tube 1c has an open end sealed by a sealant 1d of a cermet of alumina or a metal such as nickel or the like.
  • a process of manufacturing the light-emitting bulb assembly 1, including a process of manufacturing the bulb 1F and the closure 2, and the manner of supporting the main electrodes 3 with the support shafts 4 will successively be described below.
  • an aluminum salt which will become alumina having a purity of 99.98 mol % or more when thermally decomposed is used as a starting material.
  • An aluminum salt for synthesizing such highly pure alumina may be ammonium alum or aluminum ammonium carbonite hydroxysite (NH4AlCO3(OH)2).
  • the aluminum salt is then weighed, dissolved together with a dispersing agent in distilled water, thus producing a suspended aqueous solution, and then dried by a spray drying process.
  • the dried aluminum salt is thereafter thermally decomposed, thereby producing a fine powder of alumina only.
  • the dried aluminum salt is thermally decomposed at 900 ⁇ 2000°C, e.g., 1050°C, in the atmosphere for 2 hours.
  • the fine powder of alumina produced by the spray drying process and the thermal decomposition has an average particle diameter ranging from 0.2 to 0.3 ⁇ m and a purity of 99.99 mol % or higher.
  • the fine powder of alumina is thus prepared.
  • the synthesized fine powder of alumina is obtained as a secondary aggregate of fine powder of alumina having the above particle diameter, the secondary aggregate being of a size greater than the above particle diameter.
  • a fine powder of tungsten is prepared which has a purity of 99 mol % or higher and an average particle diameter of about 0.5 ⁇ m.
  • the bulb 1F and the closure 2 are fabricated of the above materials, respectively.
  • the bulb 1F is manufactured as follows: To the synthesized fine powder of alumina (secondary aggregate), there is added an organic binder which is composed primarily of an acrylic thermoplastic resin. The fine powder of alumina and the added organic binder are mixed with each other in a wet manner using an organic solvent such as of alcohol, benzene, or the like by a plastic (nylon) ball mill for about 24 hours, so that the fine powder of alumina and the organic binder are sufficiently wetted. The mixture is then distilled and dried, thereby removing the solvent, and kneaded into a compound having a desired viscosity ranging from 50,000 to 150,000 cps.
  • an organic binder which is composed primarily of an acrylic thermoplastic resin.
  • the fine powder of alumina and the added organic binder are mixed with each other in a wet manner using an organic solvent such as of alcohol, benzene, or the like by a plastic (nylon) ball mill for about 24 hours, so that the fine powder of alumina and the
  • the organic binder is a mixture of an acrylic thermoplastic resin, paraffin wax, and atactic polypropylene.
  • the total amount of the organic binder with respect to 100 g of the fine powder of alumina is 25 g.
  • the ingredients of the organic binder are of the following proportions, and adds up to the total amount (25 g) of the organic binder: Acrylic thermoplastic resin 20 ⁇ 23 g (preferably, 21.5 g) Paraffin wax 3 g or less (preferably, 2.0 g) Atactic polypropylene 2 g or less (preferably, 1.5 g)
  • the mixture is distilled and dried at 130°C for 24 hours, and thereafter kneaded at 130°C by a roll mill of alumina into the compound having the desired viscosity.
  • the compound is injection-molded into a molded body shaped as shown in Fig. 1 by a mold assembly (not shown).
  • the molded body is heated in a nitrogen atmosphere up to a temperature at which the organic binder of the acrylic thermoplastic resin, etc. is thermally decomposed and fully carbonized, so that the molded body is degreased.
  • the specific upper limit temperature up to which the molded body is to be heated in this initial heat treatment may be determined depending on the capability of a heat treatment furnace used and the temperature at which the organic binder is thermally decomposed. In this embodiment, the molded body is heated from room temperature (20°C) to 450°C in 72 hours. Other processing conditions are given below.
  • Processing pressure 1 ⁇ 8 kg/cm2 (optimum pressure: 8 kg/cm2) Time required to heat the molded body from 20°C to 450°C 72 hours or shorter
  • the added organic binder composed of an acrylic thermoplastic resin, paraffin wax, and atactic polypropylene is thermally decomposed and carbonized, so that the molded body is degreased.
  • the molded body (degreased body) is fired in the atmosphere by subsequent heat treatment under conditions given below, thereby producing a fired body.
  • the molded body is heated at a rate of 100°C/hour. Processing temperature 1200 ⁇ 1300°C (optimum temperature: 1235°C) Time during which the molded body body from 20°C processing temperature 0 ⁇ 4 hours (optimum time: 2 hours).
  • the molded body is fired by the subsequent heat treatment in the temperature range of from 1200 to 1300°C for the reasons that the density of the fired molded body will be 95 % or more of the theoretical density for being subject to subsequent hot isostatic pressing, and large crystals will not be produced in the fired body. If the molded body were fired at a temperature lower than 1200°C, then the density of the fired molded body would be less than 95 % of the theoretical density and the molded body would not be subject to hot isostatic pressing. If the molded body were fired at a temperature higher than 1300°C, then the fired body would have large crystals at a greater frequency, and would not be sufficiently strong.
  • the molded body is thus fired after it is degreased by the initial heat treatment and the subsequent heat treatment.
  • the volume of the molded body thus fired is reduced such that the volume of the molded body is 82.5 % of the volume of the molded body before it is fired.
  • the packing ratio of the fired body is about 100 % (bulk density: 3.976). Until the subsequent heat treatment is completed, the carbonized material which has been modified in the initial heat treatment is completely burned away.
  • the fired body is subjected to hot isostatic pressing in an argon atmosphere or an argon atmosphere which contains 20 vol. % or less of oxygen under conditions given below. At this time, the fired body is heated at a rate of 200°C/hour. The fired body thus pressed exhibits a light-transmitting ability. Processing temperature 1200 ⁇ 1250°C (optimum temperature: 1230°C) Processing pressure 1000 ⁇ 2000 atm (optimum pressure: 1000 atm) Processing time 1 ⁇ 4 hours (optimum processing time: 2 hours)
  • the fired body is subjected to hot isostatic pressing in the above temperature range and pressure range in order to achieve a desired high light-transmitting ability and improve its mechanical strength to avoid damage during the hot isostatic pressing. If the hot isostatic pressing were carried out at a temperature lower than 1200°C or under a pressure lower than 1000 atm, then though the fired body would be rendered light-transmissive, but the obtained light-transmitting ability would be low. If the hot isostatic pressing were carried out at a temperature in excess of 1250°C, then abnormal grain growth would be accelerated, inviting a reduction in the mechanical strength and the light-transmitting ability. If the hot isostatic pressing were carried out under a pressure in excess of 2000 atm, then stresses would concentrate in regions where bores and flaws, even if extremely small, are located in the fired body, tending to cause the fired body to crack in those regions.
  • the ends of the fired body are ground by a diamond grinding wheel (not shown) to remove edges, thereby completing the light-transmissive bulb 1F of alumina.
  • the light-transmissive bulb 1F with the electrode holding holes 1a, 1b defined in its respective opposite ends is fabricated.
  • the inner and outer surfaces of the bulb 1F thus produced are then ground by a brush with a diamond grinding grain having a particle diameter of 0.5 ⁇ m until the bulb 1F will have a wall thickness of 0.2 mm or less.
  • a brush with a diamond grinding grain having a particle diameter of 0.5 ⁇ m until the bulb 1F will have a wall thickness of 0.2 mm or less.
  • the bulb 1F includes a light-emitting region having an inside diameter of about 4.0 mm, a wall thickness of about 0.3 mm, an entire length of about 40 mm, and has properties given below.
  • TEM transmission electron microscope
  • the diameter of the electrode holding hole 1b is about 1 mm or less.
  • the particle diameter was calculated by lapping, with a diamond grinding grain, the surfaces of the specimen fabricated so that its shape, thickness, etc. were according to JIS R1601, subjecting the specimen to grain boundary etching with dissolved potassium hydroxide, observing the surfaces of the specimen with a scanning electron microscope, and analyzing the image of profiles of crystal grains.
  • the crystal grains were assumed to be spherical or polygonal in shape, and their diameters and the maximum value of inter-vertex distances were used to calculate particle diameters.
  • the linear transmittance was measured by lapping the opposite surfaces of the fabricated specimen, 0.5 mm thick, and thereafter determining the linear transmittance with a double-beam spectrophotometer.
  • the completed bulb 1F made of light-transmissive alumina has smaller crystal grain diameters than general light-transmissive ceramics which are produced by firing alumina with a sintering additive of MgO or the like for greater crystal grains (see Fig. 2).
  • the bulb 1F fabricated from highly-pure alumina has a light-transmitting ability while having small crystal grain diameters different from those of general light-transmissive ceramics for the following reasons: Since only a small amount of oxide such as MgO or the like mixed as an impurity (a total of 0.01 mol % or less at maximum) is contained in the powder of alumina, the impurity forms in its entirety a solid solution with alumina, producing almost no grain boundary phase. Therefore, the effect of a grain boundary phase which is responsible for diffusing light in general light-transmissive alumina is eliminated, resulting in an increase in the linear transmittance with respect to visible light.
  • oxide such as MgO or the like mixed as an impurity
  • n (D/d)2
  • the lattice constants of various light-transmissive aluminas obtained from highly pure alumina were determined using an X-ray diffraction apparatus, and the diameters d of the crystallites of the light-transmissive aluminas having the above average particle diameters were calculated from diffraction peaks (012) according to the Scherrer's equation which relates the diameter d of a crystallite to the width of a diffraction line.
  • the Scherrer's equation is given in P. Gallezot, "Catalysis, Science and Technology", vol. 5 p. 221, Springer-Verlag (1984), and P. Scherrer, "Gottinger Nachrichen", 2, 98 (1918).
  • a crystallite boundary in a crystal grain is nothing but such a region where the arrangement of atoms is discontinuous, it causes a diffusion of light. Consequently, the fewer the crystallite boundaries in a crystal grain, i.e., the smaller the diameter D of a crystal grain, the smaller the effect of the crystallite boundaries which are responsible for diffusing light, giving rise to an increase in the linear transmittance with respect to visible light.
  • closures 1, 1A are manufactured as described below. A process of manufacturing the closures will be described below with reference to Fig. 3.
  • a vehicle to be used to suspend therein the fine powder of alumina (secondary aggregate) synthesized as described above and the fine powder of tungsten is prepared from various organic materials given in Table 1 below (step 1).
  • the organic materials are weighed and uniformly mixed by a mixer.
  • Table 1 Ingredients Volume ratio ⁇ -terpineol 50 butyl acetate carbitol 20 ethyl cellulose 3 polyvinyl butyral 7 ethanol 10
  • the fine powder of alumina, the prepared vehicle, an organic solvent (butyl diphthalate), and a dispersing agent (ammonium carboxylic acid) are mixed at volume ratios given in Table 2, below, and kneaded into an alumina slurry by three rolls (step 2).
  • Table 2 Ingredients Volume ratio fine powder of alumina 64 vehicle 32 butyl diphthalate 3.5 ammonium carboxyl acid 0.5
  • the fine powder of tungsten, the prepared vehicle, an organic solvent (butyl diphthalate), and a dispersing agent (ammonium carboxylic acid) are mixed at volume ratios given in Table 3, below, and kneaded into a tungsten slurry by three rolls (step 2).
  • Table 3 Ingredients Volume ratio fine powder of tungsten 82 vehicle 15 butyl diphthalate 2.6 ammonium carboxyl acid 0.4
  • tungsten/alumina alumina slurry prepared at the volume ratios given in Table 2 and the tungsten slurry prepared at the volume ratios given in Table 3, eight slurries composed of tungsten and alumina mixed at volume ratios (tungsten/ alumina) given in Table 4, below, are prepared (step 3).
  • Table 4 Slurries Volume ratio (tungsten/alumina) 1st layer slurry 80/20 2nd layer slurry 60/40 3rd layer slurry 40/60 4th layer slurry 30/70 5th layer slurry 20/80 6th layer slurry 10/90 7th layer slurry 5/95 8th layer slurry 3/97
  • each of the mixed slurries thus prepared is sufficiently mixed such that alumina and tungsten are uniformly dispersed, and thereafter debubbled (step 4). More specifically, each of the mixed slurries is put in a resin container in a vacuum desiccator, and air in the vacuum desiccator is drawn out by a vacuum pump for a few tens of minutes (e.g., about 20 minutes) while the slurry in the resin container is being stirred by a magnet stirrer or the like. While the slurry is being debubbled in vacuum, the organic solvent is partly volatilized to achieve a slurry viscosity of 30,000 cP.
  • the mixed slurries shown in Table 4 are concentrically deposited to a predetermined thickness on the outer circumferential surface of each of the support shafts 4 supporting the main electrodes 3, which serves as cores of the closures.
  • the mixed slurries shown in Table 4 are applied in a descending order of volume ratios of tungsten, i.e., from the first layer slurry to the eighth layer slurry.
  • a laminated body 20 as a precursor of each of the closures 2, 2A is thus formed around the support shafts 4 as shown in Fig. 4 (step 5).
  • the mixed slurries are applied to and deposited on the outer circumferential surface of each of the support shafts 4 in the order from the first layer slurry to the eighth layer slurry by coating and drying each of the slurries successively from the first layer slurry.
  • an innermost layer composed of the first layer slurry is formed in a core-side region of the closure which is located adjacent to the core, a plurality of intermediate layers composed of the second through seventh layer slurries are formed in an intermediate region of the closure, and an outermost layer composed of the eighth layer slurry is formed in a bulb-side region of the closure which is located adjacent to the open end of the bulb.
  • Figs. 5(a), 5(b), and 5(c) are a cross-sectional view showing the structure of the closure and diagrams showing the relationship between volume ratios of tungsten and alumina in each of the layer slurries of the closure.
  • the closure 20 is of such composition distributions that the volume ratio of alumina increases up to about 100 % outwardly from the support shaft 4 as shown in Fig. 5(c), and the volume ratio of tungsten decreases from 80 % outwardly from the support shaft 4 as shown in Fig. 5(b).
  • the laminated body 20 is heated to 600°C for 10 hours in a moisture-containing hydrogen reducing atmosphere, so that the laminated body 20 is degreased (step 6). Specifically, when the laminated body 20 is heated, the organic materials and organic solvent which are contained in the vehicle that were added when the slurries were prepared are thermally decomposed and carbonized, thereby degreasing the formed body.
  • the degreased laminated body 20 is subsequently heated to 1800°C for 2 hours in a vacuum atmosphere, so that the laminated body 20 (degreased body) is fired (step 7).
  • Each of the closures 2, 2A is now obtained as the fired laminated body 20.
  • the carbonized materials modified in the above initial heat treatment are fully burned away.
  • a network structure of crystals is formed between common ingredients by firing, thereby integrally joining the ingredients.
  • a firing process for reducing surface energy is applied to the joining of the support shafts 4 and the surfaces of the electrode holding holes 1a, 1b of the bulb 1F to each other. Impurities such as of glass are often added in a small amount in an effort to accelerate the firing process.
  • the alumina forms a solid solution and is crystallized, trapping the powder of tungsten, in each layer of the laminated body 20.
  • Adjacent layers of the laminated body 20 are integrally joined to each other in solid phase as the alumina in the layers forms a solid solution and is crystallized at the mating surfaces of the layers.
  • the support shaft 4 and the innermost layer composed of the first layer slurry are also integrally joined to each other in solid phase because alumina in the innermost layer is crystallized in contact with the support shaft 4, forming a glassy substance in its grain boundaries, and also because tungsten is contained in both the support shaft 4 and the innermost layer.
  • the fired closures 2, 2A are strongly bonded to the support shafts 4 which support the main electrodes 3, hermetically sealing and securing the support shafts 4 and hence the main electrodes 3 in the bulb 1.
  • the distribution of coefficients of thermal expansion from the support shaft 4 through the innermost layer and the intermediate layers to the outermost layer is a gradient distribution ranging from the coefficient of thermal expansion of the support shaft 4 (the coefficient of thermal expansion of tungsten) to a coefficient of thermal expansion which is close to the coefficient of thermal expansion of the bulb 1F (the coefficient of thermal expansion of alumina), based on the composition distributions thereof.
  • the outer circumferential surfaces of the outermost layers of the closures 2, 2A are cut or ground so as to fit in the electrode holding holes 1a, 1b in the bulb 1F (step 8).
  • the closures are now completed, and the manufacturing process is ended.
  • the closure 2A (identical to that shown in Figs. 4 and 5) which has been fired and machined on its outer circumferential surface is fitted in the electrode holding hole 1b in the bulb 1F, bringing the outer circumferential surface of the closure 2A into contact with the inner circumferential surface of the electrode holding hole 1b. Thereafter, an infrared radiation or high-output laser beam is locally applied to the contacting surfaces to heat them.
  • the localized heating causes the alumina in the outermost layer composed of the eighth layer slurry of the closure 2A and the alumina in the bulb 1F to be fired and crystallized, and also causes grain boundaries in the joined surfaces to be embedded by a glass phase that is primarily of a structure of spinel, garnet or the like.
  • the closure 2A and the bulb 1F are therefore joined in solid phase to each other.
  • the closure 2A and the bulb 1F are hermetically secured to each other by the formation of a glass phase in the grain boundaries of alumina in the outermost layer and the bulb 1F.
  • the closure 2 (see Figs. 4 and 5) which has been fired and machined on its outer circumferential surface is fitted in the electrode holding hole 1a in the bulb 1F, and an infrared radiation or high-output laser beam is locally applied to the contacting surfaces to heat them.
  • the closure 2A and the bulb 1F are integrally joined in solid phase to each other.
  • the bulb 1F is now ready for being filled with a starting rare gas metal and a discharging material.
  • an amalgam of a given starting rare gas metal and a discharging material (an alloy of Sn, Na-T1-In, Se-Na, Dy-T1, or a halide of each of the metals) is introduced through the slender introduction tube 1c into the bulb 1F whose ends have been sealed, and thereafter the slender introduction tube 1c is sealed by the sealant 1d.
  • the closures 2, 2A and the bulb 1F are integrally joined in solid phase to each other without use of soldering glass which has heretofore been relied upon, the materials which have been sealed in the bulb 1F are reliably prevented from leaking out.
  • the bulb 1F with the main electrodes mounted therein are generally incorporated in an outer tube of a high-pressure discharge lamp such as a metal halide lamp or the like.
  • Light-emitting bulb assemblies inventive examples in which the volume ratios of tungsten in the innermost layer or the volume ratios of alumina in the outermost layer of the closure 2 according to the first embodiment are of various values which fall in the range according to the present invention, light-emitting bulb assemblies (comparative examples) in which these volume ratios are of values which fall out of the range according to the present invention, and light-emitting bulb assemblies (conventional examples) in which the closure of alumina is fixed to the bulb by alumina cermet will be compared with each other. Results of the comparison are given in Tables 5 and 6 below.
  • Each of the light-emitting bulb assemblies has a bulb which is identical to the bulb according to the first embodiment of the present invention.
  • the closures have various numbers of layers including innermost, outermost, and intermediate layers.
  • the volume ratios of alumina and tungsten from the innermost layer through the intermediate layers to the outermost layer are of distributions having increasing and decreasing gradients.
  • the durability of the light-emitting bulb assemblies was evaluated according to an accumulation of energization periods (energization service life) by applying repeatedly turning them on for 5 hours and turning them off for 0.5 hour for thereby developing thermal stresses in the light-emitting bulb assemblies.
  • Each of the light-emitting bulb assemblies was turned on by a voltage of 100 V (100 W) applied between the main electrodes 3 across a discharging material of Hg - T1I3 (0.11 g) sealed in the bulb. Since the stably energized state becomes greatly unstable in the event of a leakage of the sealed materials, the accumulation of energization periods was interrupted at the time the energized state became unstable.
  • Type Tungsten/alumina volume ratio Number of layers Energization service life Innermost layer Outermost layer 1 Inventive 55/45 3/97 7 3500 2 Inventive 65/35 3/97 8 4300 3 Inventive 75/25 3/97 9 5200 4 Inventive 85/15 3/97 10 8000 5 Comparative 35/65 3/97 4 *1 6 Comparative 45/55 35/65 3 3000 7 Conventional - - - 3000 *1 ⁇ Unable to measure due to a conduction failure.
  • the light-emitting bulb assembly according to the present invention has very high durability even when repeatedly turned on and off.
  • the light-emitting bulb assembly according to the present invention has increased resistance against thermal stresses because the closures 2, 2A are joined in solid phase which have a gradient coefficient of thermal expansion that is closer to the coefficient of thermal expansion of either the support shafts 4 with the main electrodes 3 on their distal ends or the bulb 1F toward the support shafts 4 and the bulb 1F. Because of such increased resistance against thermal stresses, the light-emitting bulb assembly is capable of highly reliable light emission and has a long service life. The light-emitting bulb assembly can also be made available with ease.
  • the light-emitting bulb assemblies according to the inventive examples with the discharging material of Hg - T1I3 (0.11 g) sealed in the bulb had a luminance of 183,000 nt
  • the light-emitting bulb assemblies according to the inventive examples with the discharging material of Hg - T1I - NaI - InI3 (0.13g) sealed in the bulb had a luminance of 240,000 nt.
  • the bulb 1F according to this embodiment is made of light-transmissive alumina composed of small crystal grains having an average particle diameter of about 0.7 ⁇ m and a maximum particle diameter of about 1.4 ⁇ m and does not form any grain boundary phase, the mechanical strength (bending strength, Weibull coefficient) in a range from room temperature to a temperature upon discharging is higher than a general bulb assembly of light-transmissive ceramics which are produced by firing alumina with a sintering additive of MgO or the like for greater crystal grains.
  • the light-emitting bulb assembly with the bulb 1F according to the present embodiment has a reduced wall thickness as well as an increased service life.
  • the starting time required for the discharging metal component to be evaporated up to a saturated vapor pressure until energization of the bulb assembly becomes stable is shortened.
  • the diffusion of light caused while the light passes through the wall of the bulb 1F is suppressed, and the bulb 1F has high linear transmittance of 70 % or more with respect to light (visible light) having a wavelength ranging from 380 to 760 nm (linear transmittance with respect to light having a wavelength of 500 nm: 82 %, thickness: 0.5 mm). Therefore, a high-pressure discharge lamp having the light-emitting bulb assembly 1 with the bulb 1F has increased luminance.
  • the highly luminous discharge lamp can have an increased service life as the discharging metal vapor components are prevented from leaking out of the bulb wall even though the bulb wall has a reduced wall thickness.
  • the electrode holding hole 1b is of a small diameter to reduce the amount of the sealant used for thereby suppressing any erosion of the sealant with the discharging metal vapor components (ions), so that any leakage of the discharging metal vapor components is avoided more reliably.
  • a second embodiment of the present invention will be described below. Closures of a light-emitting bulb assembly according to the second embodiment are different as to a process of manufacturing them and their structure from the closures of the light-emitting bulb assembly according to the second embodiment. The different process and structure will be described below.
  • Components according to the second embodiment are denoted by reference numerals which are identical to those of the components according to the first embodiment, with a suffix "a".
  • the materials of the closure 2a are also a fine powder of highly pure alumina synthesized by drying an aqueous solution of suspended aluminum salt according to a spray drying process and then thermally decomposing the aluminum salt, and a fine powder of highly pure tungsten.
  • tungsten/ alumina tungsten/ alumina
  • the ratio (volume ratio) at which the dispersing agent of ammonium carboxylic acid is added to the fine powders in each of the slurries is 2 g with respect to 100 g of the total fine powders in each of the slurries.
  • each of the slurries is debubbled (step 2). Specifically, each of the slurries taken from the ball mill is put in a resin container in a vacuum desiccator, and air in the vacuum desiccator is drawn out by a vacuum pump for a few tens of minutes (e.g., about 20 minutes) while the slurry in the resin container is being stirred by a magnet stirrer or the like.
  • a desired molded body 20a shown in Fig. 7 is produced using a mating mold assembly 10 shown in Fig. 8(a) according to a process described below.
  • the ratio of vertical and horizontal dimensions of the molded body 20a and the closure 2a shown in Figs. 7 and 10(a), 10(b) is not 1 : 1 for illustrative purpose.
  • the mating mold assembly 10 comprises a pair of symmetric molds 11a, 11b each made of a porous inorganic material such as plaster or the like or a porous resin with minute pores which has substantially the same function as plaster.
  • the molds 11a, 11b are joined to each other, defining a slurry pouring space 13 between mating surfaces of the molds 11a, 11b as shown in Fig. 8(a).
  • the molds 11a, 11b have respective grooves (cavities) 13a, 13b defined in the respective mating surfaces 15a, 15b and curved in the vicinity of lower mold ends.
  • the grooves 13a, 13b are cut in the respective mating surfaces 15a, 15b by an end mill having a spherical cutter on its distal end.
  • the grooves 13a, 13b may initially be formed in the respective mating surfaces 15a, 15b.
  • the debubbled slurries are poured in a descending order of contents of alumina, i.e., from the eleventh slurry to the first layer slurry, into the slurry pouring space 13 of the mating mold assembly 10 (step 3).
  • a cylindrical member 17 is placed on the upper surface of the mating mold assembly 10, and the eleventh slurry, which is of an amount greater than the volume of the slurry pouring space 13, is poured into the cylindrical member 17.
  • An annular piece of clay 19 is applied to the lower end of the cylindrical member 17 to provide a seal between the lower surface of the cylindrical member 17 and the upper surface of the mating mold assembly 10.
  • the clay may be replaced with rubber.
  • the poured eleventh slurry is left for a predetermined period of time.
  • the solvent (distilled water) of the eleventh slurry is drawn into the pores of the porous molds 11a, 11b by capillary action. Accordingly, a powder (alumina powder in the eleventh slurry) bounded by the dispersing agent of ammonium carboxylic acid is uniformly deposited on the wall surface of the slurry pouring surface 13, forming a thin layer 11S thereon as shown in Figs. 10(a) and 10(b).
  • the period of time during which the poured eleventh slurry is left after the eleventh slurry has been poured into the slurry pouring space 13 governs the thickness of the thin layer 11S.
  • the period of time during which the poured eleventh slurry is left is experimentally determined so that the formed thin layer 11S has a predetermined value.
  • the period of time during which the poured eleventh slurry is left and the slurry pouring space 13 are determined also in view of volume shrinkage after firing.
  • the period of time during which the poured eleventh slurry is left according to this embodiment is adjusted so that the formed thin layer 11S has a predetermined value.
  • a negative pressure may be maintained outside of the molds for forcibly drawing the solvent of the slurry out of the molds. This allows the poured eleventh slurry to be left for a shorter period of time, permits the slurry to be directly debubbled through the molds, and also makes it possible to increase the filling ratio by strongly drawing the solvent.
  • the eleventh slurry remaining inside the cylindrical member 17 and on the inner surface of the thin layer 11S is discharged. Then, the tenth slurry is poured, left for a predetermined period of time, and discharged. Thereafter, the ninth through first slurries are also poured, left for a predetermined period of time, and discharged.
  • the powders in the slurries (the power of alumina alone, the powder of mixed alumina and tungsten, and the powder of tungsten alone) are uniformly deposited in layers, forming thin layers 11S, 10S, 9S, ⁇ , 1S successively on the wall surface of the slurry pouring space 13.
  • These thin layers 11S, 10S, 9S, ⁇ , 1S jointly form a molded body 20a as a precursor of the closure 2a.
  • Figs. 12(a) and 12(b) are diagrams showing the relationship between volume ratios of tungsten and alumina in each of the thin layers.
  • the molded body 20a is of such composition distributions that the volume ratio of alumina increases from 0 % up to 100 % from the central thin layer 1S toward the outer thin layers as shown in Fig. 12(b), and the volume ratio of tungsten decreases from 100 % to 0 % from the central thin layer 1S toward the outer thin layers as shown in Fig. 12(a).
  • the thin layer 2S in the molded body 20a corresponds to the innermost layer (or the core-side layer) of the laminated body 20 according to the preceding embodiment
  • the thin layer 11S corresponds to the outermost layer (or the bulb-side layer) of the laminated body 20 according to the preceding embodiment
  • the thin layers 3S ⁇ 10S correspond to the intermediate layers of the laminated body 20 according to the preceding embodiment.
  • the thin layers 2S ⁇ 10S are disposed around and covers the central layer 1S.
  • the mating mold assembly 10 is separated, releasing the molded body 20a shaped as shown in Fig. 7.
  • the molded body 20a is dried until the solvent is thoroughly removed therefrom (step 4).
  • the molded body 20a is heated to 600°C for 10 hours in a moisture-containing hydrogen reducing atmosphere, so that the molded body 20a is degreased and temporarily fired (step 5). Specifically, when the molded body 20a is heated, the dispersing agent which was added when the slurries were prepared is thermally decomposed, thereby degreasing the molded body 20a.
  • support holding holes 21a, 21b are defined respectively in the opposite ends of the molded body 20a, and a support shaft 4 which supports a main electrode 3 is fitted in the support holding hole 21a that is defined in the distal end of the central layer 1S, and a shaft 5 of tungsten is fitted in the support holding hole 21b, thereby setting the main electrode 3 (step 6).
  • the molded body 20a with the main electrode 3 set is subsequently heated to 1500°C for 2 hours in a vacuum atmosphere, so that the molded body 20a is fired (step 7).
  • the closure 2A is now obtained as the fired molded body 20a. Until this subsequent heat treatment is completed, the carbonized materials modified when the molded body is degreased are fully burned away.
  • the thin layers of the molded body 20a are integrally joined in solid phase as with the laminated body 20 according to the preceding embodiment.
  • the support shaft 4, the shaft 5, and the thin layer 1S are also integrally joined in solid phase by volume shrinkage upon firing and coexistence of tungsten.
  • the fired closure 2a is firmly bonded to the support shaft 4 which supports the main electrode 3 and the shaft 5, hermetically sealing and securing the support shaft 4 and the main electrode 3.
  • the closure 2a is now completed, and the process of manufacturing same is completed in its entirety.
  • the outside diameter of the fired closure 2a is determined by the diameter of the slurry pouring space 13 which takes into account volume shrinkage upon firing. Therefore, the fired closure 2a is not required to be machined at its outer circumferential surface.
  • the distribution of coefficients of thermal expansion from the support shaft 4 through the thin layers 2S through 9S to the thin layer 10S is a gradient distribution ranging from the coefficient of thermal expansion of the support shaft 4 (the coefficient of thermal expansion of tungsten) to the coefficient of thermal expansion of the bulb 1F (the coefficient of thermal expansion of alumina), based on the composition distributions thereof.
  • the completed closure 2a is fitted in the electrode holding hole 1a in the bulb 1F, and then an infrared radiation or high-output laser beam is locally applied to the contacting surfaces of the closure 2a and the bulb 1F to heat them.
  • the localized heating causes the alumina in the thin layer 10S of the closure 2a and the alumina in the bulb 1F to form a glass phase in the grain boundaries in the joined surfaces.
  • the closure 2a and the bulb 1F are therefore joined in solid phase to each other.
  • the closure 2a and the bulb 1F are hermetically secured to each other.
  • a starting rare gas metal and a discharging material are filled in the bulb 1F.
  • the light-emitting bulb assembly shown in Fig. 14 is now completed.
  • the light-emitting bulb assembly with the closure 2a was also measured for its energization service life when repeatedly turned on and off. As a result, it was found that the light-emitting bulb assembly with the closure 2a also had very high durability as with the light-emitting bulb assembly with the closure 2.
  • the light-emitting bulb assembly with the closure 2a has increased resistance against thermal stresses because the closure 2a has a gradient coefficient of thermal expansion that is closer to the coefficient of thermal expansion of either the support shaft 4 having the main electrode 3 or the bulb 1F toward the support shaft 4 and the bulb 1F. Because of such increased resistance against thermal stresses, the light-emitting bulb assembly is capable of highly reliable light emission and has a long service life. The light-emitting bulb assembly can also be made available with ease.
  • the light-emitting bulb assembly with the closure 2a also offers the following advantages: Since the volume ratio of alumina is 100 % in the thin layer 11S which is exposed in the bulb 1F in supporting the main electrode 3 in the bulb 1F, i.e., the thin layer 11S is an insulation, back arcs from the main electrode 3 can be avoided for more stable energization of the light-emitting bulb assembly.
  • the main electrode 3 and the shaft 5 which serves as an external terminal are hermetically sealed by the thin layer (central layer) 1S whose volume ratio of tungsten is 100 %, a desired voltage can be applied to the main electrode 3 without fail.
  • the thin layers are formed by pouring slurries, it is possible to uniformize the thicknesses of the thin layers for reliably maintaining composition distributions in the layers and a gradient distribution of coefficients of thermal expansion.
  • the materials of the bulb 1F, the closure 2, and the closure 2a include a fine powder of alumina whose purity is 99.99 mol % or higher in the above embodiments.
  • the material is not limited to such a fine powder of alumina.
  • the bulb 1F may be in the form of a fired body composed primarily of an oxide such as alumina, magnesia, zirconia, or yttria and a nitride such as aluminum nitride, with a compound (sintering additive) added for suppressing abnormal grain growth and accelerating firing.
  • the closures 2, 2a may be fabricated using the same fine powder of ceramic as the bulb 1F thus produced. More specifically, the bulb 1F may be made of a fine powder of alumina having a purity of 99.2 mol % and an average particle diameter ranging from 0.3 to 1.0 ⁇ m, and the closures 2, 2a may be made of such a fine powder of alumina and a fine powder of tungsten.
  • the materials of the closures 2, 2a include a fine powder of tungsten in the above embodiments
  • the materials of the closures 2, 2a may be modified depending on the material of the support shaft 4 which serves as a core.
  • the support shaft 4 is made of niobium
  • the materials of the closures 2, 2a may include a fine powder of niobium.
  • the bulb may be of any of various shapes.
  • the bulb may be of a cylindrical shape with its both ends being simply open or may be a curved bulb.
  • each of the mixed slurries is coated and dried in forming the laminated body 20 around the support shaft 4 of tungsten which supports the main electrode 3.
  • green sheets may be produced from the respective mixed slurries, and successively wound around the support shaft 4 in a descending order of volume ratios of tungsten. In this case, it is preferable to stack the green sheets such that the joined surfaces of the green sheets are alternately staggered 180° around the support shaft.
  • the contacting surfaces are locally heated. However, they may be heated in the vicinity of the support shaft 4. Even when they are heated in the vicinity of the support shaft 4, since the applied thermal energy is transmitted to the outermost layers of the closures 2, 2a, the closures 2, 2a and the bulb 1F can be joined to each other in solid phase.
  • the closures 2, 2a may be fired while the degreased closures 2, 2a are being assembled in the bulb 1F.
  • the closure 2 is assembled in the bulb 1F by being fitted in the electrode holding hole 1a. Instead, as shown in Fig. 15, the closure 2 may be held against an open end of the bulb 1F to bring the end of the bulb 1F into contact with the side of the outermost layer of the closure 2, and the contacting surfaces may be locally heated to join the closure 2 and the bulb 1F to each other in solid phase at their ends.
  • the gradient of the volume ratios of alumina and tungsten in the mixed slurries is not limited to the values indicated in the above embodiments, but may be of any of various other values.
  • the closure 2 may be made of a gradient function material whose compositional proportions vary linearly from the core toward the bulb.
  • the closure joined in solid phase to the opening of the bulb which is made of light-transmissive ceramic comprises a multilayer laminated body, and the distribution of coefficients of thermal expansion from the innermost layer near the central conductive core toward the outermost layer near the bulb is a gradient distribution ranging from the coefficient of thermal expansion of the conductive core toward the coefficient of thermal expansion of the bulb based on the gradient of composition ratios of the layers.
  • compositions of the layers may be of a gradient pattern, and the layers, and the closure and the bulb may be firmly hermetically joined to each other in solid phase.
  • the concentration of thermal stresses produced upon energization of the bulb assembly can be reduced to avoid cracks in the solid-phase joints.
  • the materials sealed in the bulb assembly are prevented from leaking out, so that the bulb assembly is capable of highly reliable light emission and has a prolonged service life.
  • the light-emitting bulb assemblies according to the above embodiments have a bulb made of light-transmissive alumina having an average particle diameter of 1 ⁇ m or less and a maximum particle diameter of 2 ⁇ m or less. Consequently, the mechanical strength of the light-emitting bulb assemblies ranging from normal temperature to a discharging temperature is higher than that of the conventional light-emitting bulb assemblies. Therefore, the wall thickness of the light-emitting bulb assemblies can be reduced to 0.2 mm or smaller, which is about 1/3 of that of the conventional light-emitting bulb assemblies.
  • the amount of light transmitted from a high-luminance discharge light-emitting bulb assembly at the time light is applied to the high-luminance discharge light-emitting bulb assembly is made substantially equal to the amount of light applied to the high-luminance discharge light-emitting bulb assembly by suppressing diffusion of light.
  • the luminance can further be increased by thinning out the wall of the bulb.
  • a plurality of suspensions with different volume ratios are prepared, a laminated closure having a gradient distribution of coefficients of thermal expansion is fabricated using the prepared suspensions, and the closure and a bulb are firmly hermetically joined in solid phase to each other.
  • a laminated closure having a gradient distribution of coefficients of thermal expansion may separately be fired and fabricated, and joined in solid phase to a bulb.
  • layers are successively stacked in a descending order of volume ratios of a conductive component by a simple process of coating the layers or the like, for thereby easily producing an unfired laminated body which is a precursor of a laminated closure having a gradient distribution of coefficients of thermal expansion.
  • the suspensions with different volume ratios are formed into respective green sheets, and layers are successively stacked in a descending order of volume ratios of a conductive component (or a core) by a simple process of winding the green sheets, for thereby easily producing an unfired laminated body which is a precursor of a laminated closure having a gradient distribution of coefficients of thermal expansion.
  • thin layers are successively stacked in an order of volume ratios of a conductive component (or a core) by repeating a simple process of pouring a suspension into a porous mold assembly, causing the solvent to penetrate into the mold assembly, and discharging the excessive suspension, for thereby easily producing an unfired laminated body which is a precursor of a laminated closure having a gradient distribution of coefficients of thermal expansion.
  • the thicknesses of the thin layers can be uniformized for reliably maintaining composition distributions in the layers and a gradient distribution of coefficients of thermal expansion.
  • the central layer capable of being connected to an external source is formed of the conductive component within the innermost layer of the closure, and a given voltage can be applied without fail through the central layer to the main electrode.
  • a sealing structure of a light-emitting bulb assembly according to a third embodiment of the present invention and a method of manufacturing such a sealing structure will be described below with reference to Figs. 16 through 19.
  • Fig. 16 is a cross-sectional view of a light-emitting bulb assembly according to the third embodiment of the present invention, particularly showing in detail a sealing structure of a bulb incorporated in an outer tube of a metal vapor discharge lamp.
  • a bulb 301 has openings 302 defined respectively in its opposite ends.
  • End caps 303 as closures are integrally attached to the respective open ends 302, and electrode rods 304 as cores of the closures extend through and are held by the end caps 303, respectively.
  • the bulb 301 is made of light-transmissive polycrystalline alumina
  • the electrode rods 304 are made of a tungsten-base material of W/Th or the like which is highly resistant to light-emitting substances.
  • Each of the electrode rods 304 has an externally threaded portion 305 threaded in the corresponding end cap 303 and a flange 306 held against an outer end surface of the end cap 303.
  • the flange 306 has an outer surface sealed by a sealant 307 such as of platinum solder or glass, and one of the electrode rods 304 has a hole 308 defined therein for introducing amalgam.
  • each of the end caps 303 is of a multilayer structure as with the above embodiments. More specifically, each of the end caps 303 is composed of a plurality of layers 3031, 3032, ⁇ , 303 n arranged along the axial direction of the bulb 1.
  • the layer 3031 (the bulb-side region layer) joined to the open end 302 of the bulb 301 has a coefficient of thermal expansion which is substantially the same as that of the light-transmissive alumina of which the bulb 301 is made.
  • the outermost layer 303 n (the core-side region layer) has an internally threaded surface 309 in which the externally threaded portion 305 of the electrode rod 304 is threaded.
  • the outermost layer 303 n has a coefficient of thermal expansion which is substantially the same as that of the electrode rod 304.
  • the compositional proportions of the intermediate layers 3032, ⁇ , 303 n-1 (intermediate region layers) interposed between the layers 3031, 303 n are adjusted such that the intermediate layers 3032, ⁇ , 303 n-1 have respective coefficients of thermal expansion varying gradually from that of the innermost layer 3031 toward that of the outermost layer 303 n .
  • the thicknesses of the respective layers increase progressively from the innermost layer 3031 toward the outermost layer 303 n . This is effective to reducing stresses that are developed when the layers are thermally expanded.
  • a tapered gap 310 is defined between the electrode rod 304 and the layers 3031, ..., 303 n-1 except the outermost layer 303 n .
  • the tapered gap 310 prevents the layers 3031, ⁇ , 303 n-1 from contacting the electrode rod 304 when the lamp is assembled.
  • slips for fabricating the end caps 303 are prepared.
  • Material powders are weighed for obtaining desired coefficients of thermal expansion, and distilled water, a commercially available dispersing agent and a binder are added to the weighed material powders. They are then uniformly mixed for 24 hours by a ball mill, thereby producing slips S1 ⁇ S n respectively in the containers C1 ⁇ C n .
  • Table 7 shows compositional proportions of material powders of respective slips for an end cap 303 which is composed of a total of eleven layers.
  • the compositional proportions are represented by weight %, and the slip No. corresponds to the number of a layer of the end cap 303.
  • a tubular mold 312 is set on a porous plate or plaster board 311, and the slips S1 ⁇ S n prepared as described above are successively poured into the mold 312, thereby molding a laminated body.
  • the slips S1 ⁇ S n is to be poured, it is poured after the previously poured slip has lost its water content to a certain extent so that they will not be mixed with each other and the solvent of the previously poured slip will penetrate into the board 311.
  • a mold bar 313 may be set either before or after the slips are poured.
  • the laminated body is partly dried, the laminated body is removed from the mold 312.
  • the removed laminated body serves as an end cap 303 with a tapered through hole 314 defined therein as shown in Fig. 18(c).
  • the through hole 314 may be of a stepped shape as shown in Fig. 18(d).
  • a bulb 301 molded of a pure alumina slip is prepared, and the end cap 303 which is made wet is joined to an end of the bulb 301 as shown in Fig. 18(e), after which the bulb 301 and the end cap 303 are dried. At this time, the bulb 301 and the end cap 303 are unfired, and the bulb 301 is not light-transmissive.
  • the bulb 301 and the end cap 303 are degreased at 600°C for 5 hours in a moisture-containing hydrogen reducing atmosphere, and then fired at 1300°C for 5 hours in a dry hydrogen reducing atmosphere. Thereafter, the produced fired body is subjected to HIP in an argon atmosphere, and then annealed at 1150°C in a dry hydrogen reducing atmosphere, thereby producing an integral body of the light-transmissive bulb 301 and the end cap 303.
  • the hole 314 defined in the end cap 303 is tapped to produce an internally threaded surface 309, and then an electrode rod 304 is inserted and an externally threaded portion 305 of the electrode rod 304 is threaded in the internally threaded surface 309. Finally, the electrode rod 304 is fixed and sealed by a platinum solder 307, and an amalgam introduced into the bulb 301 through a hole 308 defined in the electrode rod 304 by a jig in the form of a platinum pipe. In this manner, the lamp is completed.
  • the bulb and the end cap are simultaneously fired in the illustrated embodiment, they may be separately fired and then joined to each other.
  • the bulb of alumina may be degreased and fired in the atmosphere, then subjected to HIP, and thereafter annealed into a light-transmissive bulb of alumina.
  • the end cap which is fired in the same manner as described above may not be subjected to HIP and annealed.
  • the bulb and the end cap may be joined to each other by laser heating in vacuum or at 2000°C or higher, or glass having the same coefficient of thermal expansion as alumina.
  • the glass should preferably be melted high-melting-point glass of a high softening point of 900°C or higher.
  • the end cap may be formed by a doctor blade process or an injection molding process as well as the slip casting process.
  • prepared slurries are formed into tapes of desired thicknesses, and the tapes are integrally joined together into an end cap having a gradient function by thermal compression.
  • the same slurries may be used to cast the bulb or poured into a mold and then solidified into the bulb.
  • each of the end caps which seal the open ends of a metal vapor discharge lamp is of a multilayer structure, and the coefficients of thermal expansion of the layers vary gradually from the open end of the bulb toward the core which holds an electrode, so that the end caps have a gradient function. Consequently, the end caps are effective to prevent damage due to different thermal expansions and leakage of the metal vapor sealed in the bulb.
  • Fig. 19 shows a modification of the third embodiment.
  • a bulb 301' differs from the bulb 301 shown in Fig. 16 in that the opposite ends of the bulb are not fully open, but have respective end surfaces 301a.
  • the end surfaces 301a have respective small openings as large as a larger-diameter portion of the tapered through hole 314 for allowing the electrode rods 304 to be inserted therethrough into the bulb.
  • Fig. 20 shows in cross section a light-emitting bulb assembly according to the fourth embodiment of the present invention, for being incorporated in an outer tube of a metal vapor discharge lamp.
  • the electrode sealing members 403 are made of an alumina material having a lower purity of 93 ⁇ 97 %, for example, than the bulb 401 which serves as a light-emitting body.
  • Each of the electrode sealing members 403 is of a multilayer structure which comprises a first layer 403a as a bulb-side region and a second layer 403b as a core-side region (the multilayer structure may be composed of three layers or more including an intermediate layer or layers).
  • the first layer 403a held against the inner wall surface of the bulb 401 is made of alumina having a purity of 96 %, for example, and the second layer 403b inward of the first layer 403a is made of alumina having a purity of 93 %, for example.
  • Electrode rods 404 as cores are inserted in the respective electrode sealing members 403, and caps 405 through which the electrode rods 404 extend are disposed against the open ends of the bulb 401.
  • Sealing glass 406 produced by melting and cooling a glass solder is positioned to provide a seal between the electrode sealing members 403 and the electrode rods 404, between the electrode rods 404 and the caps 405, and between the ends of the bulb 401 and the electrode sealing members 403 and the caps 405.
  • the purity of the caps 405 is preferably an average of the purities of the bulb 401 and the electrode sealing members 403.
  • the caps 405 may be dispensed with as required.
  • the electrode sealing members 403 Since a glass component is present in grain boundaries of alumina ceramics in the inner walls of the electrode sealing members 403 which are made of an alumina material having a lower purity than the bulb 401 and which are disposed in the openings of the bulb 401, the electrode sealing members 403 adhere well to the sealing glass solder, thereby improving a sealing capability.
  • a composition gradient structure made of aluminas having different purities serves to suppress the generation of thermal stresses.
  • a fine powder of alumina having a high purity of 4N or more for producing light-transmissive alumina is prepared in a container C41, and a fine powder of alumina having a lower purity (93 % in this embodiment) is prepared in a container C42.
  • the fine powder of low purity contains impurities of silica, magnesia, and so on.
  • the fine powders of alumina should preferably be selected which have similar firing behaviors.
  • an alumina slip S41 having a high purity (4N) is prepared in a container C43
  • an alumina slip S42 having a purity of 96 % is prepared in a container C44
  • an alumina slip S43 having a purity of 93 % is prepared in a container C45.
  • alumina slip S41 having a high purity is poured from the container C43 into the plaster mold assembly 411, and left for a predetermined period of time. After a highly pure alumina layer 413 has been deposited on an inner circumferential surface of the plaster mold assembly 411, the alumina slip S41 is discharged.
  • one end of the plaster mold assembly 411 is dipped in the alumina slip S42 having a purity of 96 % to deposit an alumina layer on only a sealing portion for thereby forming a 96%-alumina layer 414 on an inner circumferential surface of the highly pure alumina layer 413 as shown in Fig. 23(e).
  • a 96%-alumina layer 414 is also deposited on an inner circumferential surface of the highly pure alumina layer 413 at the other end of the plaster mold assembly 411.
  • one end of the plaster mold assembly 411 is dipped in the alumina slip S43 having a purity of 93 % to deposit an alumina layer on only a sealing portion for thereby forming a 93%-alumina layer 415 on an inner circumferential surface of the 96%-alumina layer 414 as shown in Fig. 23(f).
  • a 93%-alumina layer 415 is also deposited on an inner circumferential surface of the 96%-alumina layer 414 at the other end of the plaster mold assembly 411.
  • the formed body thus produced is fired at 1800°C for 6 hours in a hydrogen reducing atmosphere, thus producing a bulb 401 having a light-emitting portion composed of the light-transmissive alumina layer and sealing portions composed of the electrode sealing members 403 which comprise alumina layers of low purity.
  • the bulb may be fired at 1350°C for 6 hours in the air and thereafter heated at 1350°C for 2 hours under 1000 atmospheric pressures in an argon atmosphere by way of hot isostatic pressing. In this case, however, since almost no alumina of low purity is generally sintered at this temperature, the purity of alumina in the innermost layer in the sealed portions have to be 97 % or higher.
  • the bulb 401 and the electrode sealing members 403 thus produced are then machined at their inner surfaces and the light-emitting portion is machined at its outer circumferential surface, and then a metal vapor discharge lamp is assembled.
  • the electrode sealing members 523 is made of an alumina material which has a lower purity (e.g., 99 ⁇ 97 %) than the bulb 521 which serves as a light-emitting portion.
  • Each of the electrode sealing members 523 is of a laminated structure including a first layer 523a, a second layer 523b, and a third layer 523c (the laminated structure may include four or more layers) arranged along the axial direction of the bulb 521 or the electrode rods 524.
  • the first layer 523a, the second layer 523b, and the third layer 523c are progressively thicker in the direction from the first layer 523a toward the third layer 523c.
  • the third layer 523c and the second layer 523b have a greater area held against the electrode rods 524 than the first layer 523a.
  • the caps 525 are made of alumina having the same purity as that of the third layer 523c.
  • the caps 525 may be dispensed with as required.
  • a fine powder of alumina having a high purity of 4N or more for producing light-transmissive alumina, and a fine powder of alumina having a lower purity (93 % in this embodiment) are prepared.
  • an alumina slip S51 having a high purity (4N) is prepared in a container C51, an alumina slip S52 having a purity of 97 % in a container C52, an alumina slip S53 having a purity of 95 % in a container C53, and an alumina slip S54 having a purity of 93 % in a container C54.
  • a tubular mold 532 having a size matching the outside diameter of a bulb is set on a porous mold assembly or plaster mold assembly 531, and a mold bar 533 is vertically placed centrally in the mold 532.
  • the alumina slip S54 having a purity of 93 %, the alumina slip S53 having a purity of 95 %, the alumina slip S52 having a purity of 97 %, and the alumina slip S51 having a high purity are successively poured into a space defined by the mold 532 and the mold bar 533, thereby molding a laminated body.
  • each of the alumina slips is to be poured, it is poured after the previously poured slip has lost its water content to a certain extent so that they will not be mixed with each other.
  • a pipe 534 shown in Fig. 26 which will serve as the bulb 521 is formed of the highly pure alumina slip S51.
  • the pipe 534 is then inserted into the mold 532 while the highly pure alumina slip S51 for producing an end 522a of the bulb 521 is not being dried, and integrally joined to the laminated body, thereby producing a molded body as shown in Fig. 27(b). Thereafter, as with the above embodiment, the molded body is fired, machined, and assembled.
  • electrode sealing members made of an alumina material having a lower purity than a light-emitting portion are disposed on respective opposite ends of a bulb, and a glass solder or sealing glass is held in contact with the electrode sealing members to keep them out of contact with the bulb. Therefore, the sealing capability is made highly reliable for allowing the lamp to have an increased service life.
  • the composition of the electrode sealing members is of a gradient nature, the sealing capability of the sealing regions is further increased.
  • a sealing structure of a light-emitting bulb assembly for a metal vapor discharge lamp according to a sixth embodiment of the present invention and a method of manufacturing such a sealing structure will be described below with reference to Figs. 28 through 30(a) ⁇ 30(d).
  • Fig. 28 shows a bulb 601 made of light-transmissive polycrystalline alumina to be incorporated in an outer tube of a metal vapor discharge lamp. Caps 604 of alumina as closures are fitted in respective end openings 602 of the bulb 601 through sealing glass 603.
  • Each of the caps 604 comprises a high-purity alumina portion 604a, a gradient-composition portion 604b, and a low-purity alumina portion 604c.
  • the high-purity alumina portion 604a as a bulb-side region is made of Al2O3 having a purity of 99.99 % and exposed to the interior of the bulb 601.
  • the low-purity alumina portion 604c as a core-side region is made of Al2O3 having a purity of 93.0 % and exposed to the exterior of the bulb 601.
  • the gradient-composition portion 604b as an intermediate region has a section held against the high-purity alumina portion 604a and having a purity of 99.99 %, is progressively lower in purity toward the low-purity alumina portion 604c, and has a section held against the low-purity alumina portion 604c and having a purity of 93.0 %.
  • the gradient-composition portion 604b with such a continuous gradient composition has a greatly increased peeling strength.
  • the low-purity alumina portion 604c has a greater width along the axial direction of the bulb than the width of the high-purity alumina portion 604a.
  • each of the caps 604 has axial holes 605, 606 defined therein.
  • An internal electrode rod 607 is press in the hole 605, and an external electrode rod (lead) 608 is pressed in the hole 606.
  • the holes 605, 606 are such diameters which will be about 200 ⁇ m larger than electrode rods 607, 608 after being fired. This prevents the caps from being obstructed and cracked by the electrodes when fired.
  • the low-purity alumina portion 604c has a radial hole 609 defined from its side toward the inside thereof in communication with the axial hole 605.
  • a conductive film 610 of tungsten (W) or the like is disposed in the radial hole 609 and on the outer surface of the low-purity alumina portion 604c.
  • the conductive film 610 serves to provide a good electric connection between the internal electrode rod 607 and the external electrode rod 608.
  • the conductive film 610 may be made of Nb, Ta, Mo, Ni, or the like.
  • FIG. 29(a) A process of manufacturing each of the caps 604 will be described below with reference to Figs. 29(a) through 29(e).
  • 100 g of Al2O3 of a high purity (99.99 %), 100 g of Al2O3 of a low purity (93.0 %), 50 g of water, and a deflocculant are mixed for 24 hours by a ball mill, thereby producing a slip S61 of Al2O3 of a high purity and a slip S62 of Al2O3 of a low purity.
  • the slips S61, S62 are mixed with each other to produce a plurality of slips S63 having purities ranging between 99.99 % and 93.0 %.
  • the slips are successively poured, from the highly pure slip S61, into a mold 615 set on a porous body or a plaster body 614, producing a molded body 616 prior to being fired by way of one-sided deposition.
  • the molded body 616 is then temporarily fired at 1100°C for 2 hours, so that the molded body 616 has a hardness that allows the molded body 616 to be handled. Thereafter, the molded body 616 is machined to form axial holes 605, 606 and a radial hole 609, as shown in Fig. 19(d), and shaped into a cap. A conductive paste 610 is then introduced into the radial hole 609 and applied to the outer surface of the low-purity alumina portion 604c.
  • the cap 604 is inserted in one of the openings 602 of the bulb 601, and sealed by glass 603 or an alloy of a low melting point.
  • Figs. 30(a) through 30(d) show a modification of the process of manufacturing the light-emitting body according to the sixth embodiment.
  • the modified process as shown in Fig. 30(a), using two porous bodies or plaster bodies 614a, 614b and two molds 615a, 615b, a molded body 616a serving as a high-purity alumina portion and a gradient-composition portion, and a molded body 616b serving as a low-purity alumina portion are produced as shown in Fig. 30(b).
  • the surface of the molded body 616b is coated with a conductive paste, and the molded body 616a is bonded integrally to the molded body 616b by the conductive paste.
  • an internal electrode rod 607 and an external electrode rod 608 are inserted, and the assembly is fired into a cap 604 as shown in Fig. 30(d). Since the conductive paste which interconnects the molded bodies 616a, 616b provides an electric connection between the internal electrode rod 607 and the external electrode rod 608, the radial hole 609 as shown in Fig. 29(d) is not required.
  • each of caps which close respective openings of a light-emitting bulb assembly for a metal vapor discharge lamp and support internal and external electrodes separately from each other is composed of a high-purity alumina portion exposed to the interior of the bulb assembly, a low-purity alumina portion exposed to the exterior of the bulb assembly, and a gradient-composition portion interconnecting the high-purity alumina portion and the low-purity alumina portion, and a conductive film which provides an electric connection between the internal and external electrodes is disposed on the surface of the low-purity alumina portion.
  • the conductive film has a peeling strength increased to 10 kg/cm2 from a conventional value ranging from 1 to 4 kg/cm2.
  • the lamp characteristics are prevented from being degraded due to a corrosive component such as Na.
  • a corrosive component such as Na.
  • Metals such as Nb, Ta, Mo, Ti, and so on may also be used as the conductive film (metallized film).
  • a sealing structure for a light-emitting bulb assembly allows a discharge light-emitting bulb assembly to be highly reliable and have a long service life.
  • the light-emitting bulb assembly can be used in a metal-vapor discharge lamp such as a mercury-vapor lamp, a metal halide lamp, or a sodium-vapor lamp, or a high-intensity discharge lamp.
EP93914987A 1992-07-09 1993-07-09 Struktur von abtichtungsteil einer bogenröhre und verfahren zur herstellung derselben Expired - Lifetime EP0650184B1 (de)

Applications Claiming Priority (10)

Application Number Priority Date Filing Date Title
JP20609292 1992-07-09
JP20609292 1992-07-09
JP206092/92 1992-07-09
JP32367692 1992-11-09
JP323676/92 1992-11-09
JP32367692 1992-11-09
JP28682/93 1993-01-25
JP2868293 1993-01-25
JP2868293 1993-01-25
PCT/JP1993/000959 WO1994001884A1 (en) 1992-07-09 1993-07-09 Structure of sealing part of arc tube and method of manufacturing the same

Publications (3)

Publication Number Publication Date
EP0650184A1 true EP0650184A1 (de) 1995-04-26
EP0650184A4 EP0650184A4 (de) 1997-05-07
EP0650184B1 EP0650184B1 (de) 2002-06-05

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EP (1) EP0650184B1 (de)
JP (1) JP3456212B2 (de)
KR (1) KR100303570B1 (de)
AU (1) AU4514593A (de)
CA (1) CA2139839A1 (de)
DE (1) DE69331991T2 (de)
WO (1) WO1994001884A1 (de)

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5742123A (en) * 1992-07-09 1998-04-21 Toto Ltd. Sealing structure for light-emitting bulb assembly and method of manufacturing same
EP0887840A2 (de) * 1997-06-27 1998-12-30 Patent-Treuhand-Gesellschaft für elektrische Glühlampen mbH Metallhalodenidlampe mit keramischem Entladungsgefäss
EP0887838A2 (de) * 1997-06-27 1998-12-30 Osram Sylvania Inc. Vorrichtung mit Keramischem Gefäss, Lampe mit solcher Vorrichtung und Verfahren zur Herstellung solcher Vorrichtungen
US5861714A (en) * 1997-06-27 1999-01-19 Osram Sylvania Inc. Ceramic envelope device, lamp with such a device, and method of manufacture of such devices
EP0917181A1 (de) * 1997-11-14 1999-05-19 Ngk Insulators, Ltd. Hochdruckentladungslampe und Herstellungsverfahren derselben
EP0938126A1 (de) * 1997-09-08 1999-08-25 Ushio Denki Kabushiki Kaisya Elektrizitatseinleitungselement fur gafasse
US6181065B1 (en) 1997-06-27 2001-01-30 Patent-Treuhand-Gesellschaft F. Elektrische Gluehlampen Mbh Metal halide or sodium high pressure lamp with cermet of alumina, molybdenum and tungsten
EP1107286A1 (de) * 1999-12-02 2001-06-13 Ushiodenki Kabushiki Kaisha Hochdruck-Quecksilberdampfentladungslampe
EP1367634A2 (de) * 2002-05-28 2003-12-03 Nec Corporation Hochdruckgasentladungslampe und Verfahren zu ihrer Herstellung
US6873108B2 (en) 2001-09-14 2005-03-29 Osram Sylvania Inc. Monolithic seal for a sapphire metal halide lamp
EP1585168A1 (de) * 2003-09-22 2005-10-12 Matsushita Electric Industrial Co., Ltd. Metallhalogenidlampe
WO2006046172A1 (en) * 2004-10-25 2006-05-04 Koninklijke Philips Electronics N.V. Electric discharge lamp
EP1755147A1 (de) * 2004-06-08 2007-02-21 Ngk Insulators, Ltd. Lichtemittierender behälter und lichtemittierender behälter für eine hochdruck-entladungslampe
EP1757567A1 (de) * 2004-06-08 2007-02-28 Ngk Insulators, Ltd. Sprödmaterial-metall-konstruktion
US7247591B2 (en) 2005-05-26 2007-07-24 Osram Sylvania Inc. Translucent PCA ceramic, ceramic discharge vessel, and method of making
US7843137B2 (en) * 2005-03-31 2010-11-30 Ngk Insulators, Ltd. Luminous vessels
US7897098B2 (en) 2005-03-16 2011-03-01 Osram Sylvania Inc. High total transmittance alumina discharge vessels having submicron grain size
WO2014042812A1 (en) * 2012-09-12 2014-03-20 General Electric Company Reduced mass end plugs for voidless cmh lamps

Families Citing this family (3)

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Publication number Priority date Publication date Assignee Title
JP4585823B2 (ja) * 2004-09-24 2010-11-24 東芝ライテック株式会社 管球および封止部材
US8299709B2 (en) 2007-02-05 2012-10-30 General Electric Company Lamp having axially and radially graded structure
JP5262911B2 (ja) * 2009-03-30 2013-08-14 パナソニック株式会社 放電管及び放電管の製造方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2032277A1 (de) * 1970-06-25 1971-12-30 Egyesuelt Izzolampa Stromzuführungskonstruktion fur kera mische Entladungslampen
EP0528428A1 (de) * 1991-08-20 1993-02-24 Patent-Treuhand-Gesellschaft für elektrische Glühlampen mbH Hochdruckentladungslampe und Verfahren zur Herstellung

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01302652A (ja) * 1988-05-30 1989-12-06 Toshiba Lighting & Technol Corp セラミック放電灯
JPH0215557A (ja) * 1988-07-04 1990-01-19 Toshiba Lighting & Technol Corp 高圧ナトリウムランプ
JPH06724B2 (ja) * 1988-12-08 1994-01-05 田辺製薬株式会社 ナフタレン誘導体

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2032277A1 (de) * 1970-06-25 1971-12-30 Egyesuelt Izzolampa Stromzuführungskonstruktion fur kera mische Entladungslampen
EP0528428A1 (de) * 1991-08-20 1993-02-24 Patent-Treuhand-Gesellschaft für elektrische Glühlampen mbH Hochdruckentladungslampe und Verfahren zur Herstellung

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO9401884A1 *

Cited By (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5742123A (en) * 1992-07-09 1998-04-21 Toto Ltd. Sealing structure for light-emitting bulb assembly and method of manufacturing same
EP0887837A3 (de) * 1997-06-27 1999-04-07 Osram Sylvania Inc. Keramischer Kolben, Lampe mit einem solchen Kolben und Verfahren zur Herstellung solchen Vorrichtungen
US6181065B1 (en) 1997-06-27 2001-01-30 Patent-Treuhand-Gesellschaft F. Elektrische Gluehlampen Mbh Metal halide or sodium high pressure lamp with cermet of alumina, molybdenum and tungsten
US5861714A (en) * 1997-06-27 1999-01-19 Osram Sylvania Inc. Ceramic envelope device, lamp with such a device, and method of manufacture of such devices
EP0887840A3 (de) * 1997-06-27 1999-03-24 Patent-Treuhand-Gesellschaft für elektrische Glühlampen mbH Metallhalodenidlampe mit keramischem Entladungsgefäss
EP0887838A3 (de) * 1997-06-27 1999-03-31 Osram Sylvania Inc. Vorrichtung mit Keramischem Gefäss, Lampe mit solcher Vorrichtung und Verfahren zur Herstellung solcher Vorrichtungen
EP0887840A2 (de) * 1997-06-27 1998-12-30 Patent-Treuhand-Gesellschaft für elektrische Glühlampen mbH Metallhalodenidlampe mit keramischem Entladungsgefäss
US6194832B1 (en) 1997-06-27 2001-02-27 Patent-Treuhand-Gesellschaft F. Elektrische Gluehlampen Mbh Metal halide lamp with aluminum gradated stacked plugs
EP0887838A2 (de) * 1997-06-27 1998-12-30 Osram Sylvania Inc. Vorrichtung mit Keramischem Gefäss, Lampe mit solcher Vorrichtung und Verfahren zur Herstellung solcher Vorrichtungen
US6020685A (en) * 1997-06-27 2000-02-01 Osram Sylvania Inc. Lamp with radially graded cermet feedthrough assembly
EP0938126A4 (de) * 1997-09-08 2000-04-19 Ushio Electric Inc Elektrizitatseinleitungselement fur gafasse
EP0938126A1 (de) * 1997-09-08 1999-08-25 Ushio Denki Kabushiki Kaisya Elektrizitatseinleitungselement fur gafasse
US6320314B1 (en) 1997-09-08 2001-11-20 Ushiodenki Kabushiki Kaisha Electricity introducing member for vessels
EP0917181A1 (de) * 1997-11-14 1999-05-19 Ngk Insulators, Ltd. Hochdruckentladungslampe und Herstellungsverfahren derselben
US6362567B1 (en) 1997-11-14 2002-03-26 Ngk Insulators, Ltd. High pressure discharge lamp having thermal layers manufacturing the same
US6462471B1 (en) 1999-12-02 2002-10-08 Ushiodenki Kabushiki Kaisha High pressure mercury lamp provided with a sealing body made of a functional gradient material
EP1107286A1 (de) * 1999-12-02 2001-06-13 Ushiodenki Kabushiki Kaisha Hochdruck-Quecksilberdampfentladungslampe
US6873108B2 (en) 2001-09-14 2005-03-29 Osram Sylvania Inc. Monolithic seal for a sapphire metal halide lamp
EP1367634A2 (de) * 2002-05-28 2003-12-03 Nec Corporation Hochdruckgasentladungslampe und Verfahren zu ihrer Herstellung
EP1367634A3 (de) * 2002-05-28 2006-06-07 Nec Corporation Hochdruckgasentladungslampe und Verfahren zu ihrer Herstellung
EP1585168A1 (de) * 2003-09-22 2005-10-12 Matsushita Electric Industrial Co., Ltd. Metallhalogenidlampe
EP1585168A4 (de) * 2003-09-22 2006-07-05 Matsushita Electric Ind Co Ltd Metallhalogenidlampe
CN100382228C (zh) * 2003-09-22 2008-04-16 松下电器产业株式会社 金属卤灯
EP1755147A4 (de) * 2004-06-08 2010-02-24 Ngk Insulators Ltd Lichtemittierender behälter und lichtemittierender behälter für eine hochdruck-entladungslampe
EP1755147A1 (de) * 2004-06-08 2007-02-21 Ngk Insulators, Ltd. Lichtemittierender behälter und lichtemittierender behälter für eine hochdruck-entladungslampe
EP1757567A1 (de) * 2004-06-08 2007-02-28 Ngk Insulators, Ltd. Sprödmaterial-metall-konstruktion
EP1757567A4 (de) * 2004-06-08 2011-02-02 Ngk Insulators Ltd Sprödmaterial-metall-konstruktion
WO2006046172A1 (en) * 2004-10-25 2006-05-04 Koninklijke Philips Electronics N.V. Electric discharge lamp
US7897098B2 (en) 2005-03-16 2011-03-01 Osram Sylvania Inc. High total transmittance alumina discharge vessels having submicron grain size
US7843137B2 (en) * 2005-03-31 2010-11-30 Ngk Insulators, Ltd. Luminous vessels
US7247591B2 (en) 2005-05-26 2007-07-24 Osram Sylvania Inc. Translucent PCA ceramic, ceramic discharge vessel, and method of making
WO2014042812A1 (en) * 2012-09-12 2014-03-20 General Electric Company Reduced mass end plugs for voidless cmh lamps
CN104641446A (zh) * 2012-09-12 2015-05-20 通用电气公司 用于无隙cmh灯的质量减少的端部插塞

Also Published As

Publication number Publication date
EP0650184A4 (de) 1997-05-07
KR100303570B1 (ko) 2001-12-01
CA2139839A1 (en) 1994-01-20
WO1994001884A1 (en) 1994-01-20
DE69331991D1 (de) 2002-07-11
EP0650184B1 (de) 2002-06-05
AU4514593A (en) 1994-01-31
DE69331991T2 (de) 2002-09-19
JP3456212B2 (ja) 2003-10-14

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