[go: up one dir, main page]

EP0797238B1 - Light-screening film paint for lamps, and light-screening film for lamps and producing method thereof - Google Patents

Light-screening film paint for lamps, and light-screening film for lamps and producing method thereof Download PDF

Info

Publication number
EP0797238B1
EP0797238B1 EP97104628A EP97104628A EP0797238B1 EP 0797238 B1 EP0797238 B1 EP 0797238B1 EP 97104628 A EP97104628 A EP 97104628A EP 97104628 A EP97104628 A EP 97104628A EP 0797238 B1 EP0797238 B1 EP 0797238B1
Authority
EP
European Patent Office
Prior art keywords
light
lamps
screening film
set forth
paint
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP97104628A
Other languages
German (de)
French (fr)
Other versions
EP0797238A3 (en
EP0797238A2 (en
Inventor
Tatsuo c/o Matsushita El.Ind.Co.Ltd. Mifune
Kazunori c/o Matsushita El.Ind.Co.Ltd. Sakamoto
Tsumoru c/o Matsushita El.Ind.Co.Ltd. Ohata
Masaru c/o Matsushita El.Ind.Co.Ltd. Watanabe
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP06236696A external-priority patent/JP3444086B2/en
Priority claimed from JP8305405A external-priority patent/JPH10147736A/en
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Publication of EP0797238A2 publication Critical patent/EP0797238A2/en
Publication of EP0797238A3 publication Critical patent/EP0797238A3/en
Application granted granted Critical
Publication of EP0797238B1 publication Critical patent/EP0797238B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J9/00Apparatus 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
    • H01J9/20Manufacture of screens on or from which an image or pattern is formed, picked up, converted or stored; Applying coatings to the vessel
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J61/00Gas-discharge or vapour-discharge lamps
    • H01J61/02Details
    • H01J61/30Vessels; Containers
    • H01J61/35Vessels; Containers provided with coatings on the walls thereof; Selection of materials for the coatings

Definitions

  • the present invention relates to a light-screening film paint for lamps, and to a method for producing a light-screening film having the features of the preambles of claims 1 and 13, respectively.
  • a film paint and a method having the features of the preambles of claims 1 and 13, respectively, are known from both prior art documents DD-A-102 010 and of EP-A-0 739 534, which is relevant pursuant to Articles 54(3) and (4) EPC.
  • FIG. 1 shows a structural drawing of a highly luminous D2R-type discharge lamp for automobile front lamp.
  • the discharge lamp for automobiles is so arranged as that a metal iodide sealed in a quartz emissive section 5 emits a light under application of a high tension between the metal tungsten electrodes 1a and 1b.
  • the emissive section 5 is covered with an external quartz tube 2.
  • this halogen lamp is advantageous in providing a threefold luminosity at a 70% consumed power. Beside, because of using no filament unlike halogen lights, the service life is very long and not shorter than 1,500 hours.
  • a light-screening film 4 is formed on the surface of a outer quartz tube 2 to control the project region of light.
  • This light-screening film is about 20 ⁇ m thick, the shape and size of which are specified in according with the International Standard.
  • the present invention refers also to a producing method for this light-screening film.
  • a conventional light-screening film for lamps has been formed by mixing a pigment and a binder to form a paint, applying this paint to the glass surface of a lamp and firing the coat at a temperature of 100°C to 250°C
  • the temperature of the glass surface of a lamp rises and accordingly that of the light-screening film formed thereon also rises.
  • the temperature of the glass surface of the lamp rises to about 700°C during the lighting and necessarily the light-screening film on the glass surface is also exposed to a temperature of 700°C.
  • a light-screening film uses ferric oxide or the like as pigment. Though being black at room temperature, cupric oxide is known to turn into red powder with the progress of oxidation at about 350°C.
  • the present invention employs a light-screening film paint according to claim 1 and a method according to claim 13. Preferred embodiments are disclosed in the dependent claims.
  • a paint film is formed on the glass surface by binder action of methyl cellulose, vinyl alcohol and acrylic resin.
  • methyl cellulose functions to inhibit the sedimentation, coagulation or separation of pigment powder in a paint, whereby the paint can be stabilized by adding 0.2 to 2 parts thereof to 100 parts of powder quantity.
  • thixotropy can be afforded to a paint, so that a stable application of the paint by using a coater becomes possible.
  • methyl cellulose, vinyl alcohol and acrylic resin are thermally decomposed and consequently their residue in the paint film vanishes.
  • powder glass contained in the paint melts and functions as a binder. More preferably, by using glass mainly comprising zinc oxide and silica as powder glass, a light-screening film is obtained which has a high adhesion strength to the surface of quartz glass. And more preferably, by using powder glass having a melting point of not higher than 1000°C and setting the firing temperature at not higher than 1000°C, the deterioration of lamp performance can be prevented.
  • the difference in thermal expansion coefficient from a quartz glass tube decreases and the peeling of a light-screening film due to local ups and downs of temperature caused by the lighting and extinction of a lamp hardly occurs.
  • the deterioration of light-screening film strength due to a rise in temperature caused by the lighting of a lamp after the firing can be prevented.
  • the metal electrode material for a main lamp body is kept from being oxidized, so that a light-screening film can be formed without deterioration of the lamp performance.
  • 100g of manganese oxide having a grain size distribution of 1 ⁇ m to 20 ⁇ m, 100g of iron oxide powder containing about 20 % by weight of manganese added for obtaining iron oxide from iron hydroxide and having a grain size distribution of 0.3 ⁇ m to 3 ⁇ m, and 100g of powder glass containing about 70 % by weight of zinc oxide, aluminum oxide and silica were dry-mixed in an agate mortar for one hour to make a mixture.
  • the powder glass employed is one which melts at about 700°C and crystallizes as the temperature is raised up to 750°C.
  • the light-screening film paint prepared in this way was applied to the quartz glass surface of a lamp by means of a coater and fired at 800°C for an hour after transient drying at 100°C. Firing was conducted under the vacuum atmosphere of 1 x 10 -4 Torr.
  • the light-screening film formed in this way on the glass surface of a highly luminous discharge lamp has a high adhesion strength to the lamp and the color of the whole film was black.
  • the light-screening film obtained was estimated by discoloration measurement after the lighting, film strength measurement, transmissibility measurement, and surface observation after the lighting.
  • a change in the color of a light-screening film was measured with a chroma meter and estimated in accordance with the Lab method. From changes in the respective values of L, a and b, ⁇ Eab was calculated. The passable levels for estimation were set at a ⁇ Eab value determined to be not greater than 1, calculated from measurements of the color of a light-screening film before lighting and after an 1,500-hours duration of lighting.
  • the film strength determined by the cross cut test according to the JIS (Japanese Industrial Standards) Z 1522, was examined respectively before lighting and after an 1,500-hours duration of lighting.
  • a light-screening film was cut into specimens with a diamond cutter and tapes were pasted to the respective specimens and peeled.
  • the peeling degree of the light-screening film observed at that time was examined. Only those in which no peeling whatever was observed were determined as the passable level.
  • the passable level for transmittance measurements was taken at a leaking light ratio of not greater than 0.5%.
  • FIG. 2 shows the result of discoloration measurements of the light-screening film obtained in the above embodiment.
  • a light-screening film according to the present invention has a much smaller degree of discoloration than that of a conventional one using cupric oxide as pigment and manifested a ⁇ Eab value of not greater than 1 after an 1,500-hours duration of lighting.
  • FIG. 3 shows mixing ratios of the mixture of manganese oxide powder and iron oxide powder containing about 20% by weight of manganese to powder glass mainly containing zinc oxide, and the estimation results of the obtained light-screening films. This result revealed that a good light-screening film can be obtained by mixing 30 to 100 parts of powder glass mainly containing zinc oxide with 100 parts of the mixture of manganese oxide powder and manganese-contained iron oxide powder.
  • the manganese content in manganese-contained iron oxide was 20%, but results similar to the one obtained in the above embodiment were obtained also at other ratios.
  • FIG. 4 shows these results. From FIG. 4 the most appropriate content of manganese was found to range from 5 mol% to 30 mol%.
  • powder glass mainly containing zinc oxide was employed, but powder glass mainly comprising any of zinc oxide or boron oxide or aluminum oxide or silica provided a light-screening film equivalent to the one obtained in the above embodiment.
  • powder glass that begins to melt at 700°C and is crystallized at 750°C was employed, but a light-screening films equivalent to the one obtained in the above embodiment were obtained for powder glass having other softening points.
  • FIG. 5 shows these results.
  • the firing temperature was set to the softening temperature plus 100°C. From FIG. 5 it proved appropriate that the melting point of the powder glass employed ranges from 600°C to 1,100°C, both inclusive, and the firing temperature is not higher than 1,200°C.
  • thixocity was afforded to a paint by adding one part of silica powder having a grain size of not greater than 100nm to 100 parts of powder quantity, but equivalent results were obtained also on using swelling clay minerals such as smectite containing silica in place of silica powder.
  • the powder quantity referred to here is the total quantity of a mixture comprising manganese oxide and manganese contained iron oxide and powder glass.
  • Silica powder having a larger grain size that 100nm provides no desired effect.
  • FIG. 6 revealed that 0.2 part to 2 parts of added amount to 100 parts of powder quantity is suitable for the attainment of a stable coating by the prevention of liquid dripping or the like.
  • FIG. 6 shows the results examined on swelling clay minerals containing silica, but equivalent results were obtained also for silica powder having a grain size of not greater than 100nm.
  • FIG. 7 shows the results of correspondence between the added amount of methyl cellulose.
  • the results of FIG. 7 revealed that the added amount of methyl cellulose is preferably 0.2 to 2 parts to 100 parts of powder quantity.
  • FIG. 7 shows the results in the case of methyl cellulose, but equivalent results were obtained also on using vinyl alcohol or acrylic resin in place of this.
  • firing was conducted in the atmosphere of 1 x 10 -4 Torr.
  • the degree of vacuum was found to be preferably not higher than 1 x 10 -2 Torr.
  • a favorable effect in a light-screening film formed on the glass surface of a highly luminous discharge lamp was obtained that the adhesion strength to a lamp is strong, the color of the whole film is black and neither peeling nor discoloration of the light-screening film occurs even after a 200-hours duration of lighting.

Landscapes

  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Vessels And Coating Films For Discharge Lamps (AREA)
  • Surface Treatment Of Glass (AREA)
  • Paints Or Removers (AREA)

Description

    Field of the Invention
  • The present invention relates to a light-screening film paint for lamps, and to a method for producing a light-screening film having the features of the preambles of claims 1 and 13, respectively.
  • Background of the Invention
  • A film paint and a method having the features of the preambles of claims 1 and 13, respectively, are known from both prior art documents DD-A-102 010 and of EP-A-0 739 534, which is relevant pursuant to Articles 54(3) and (4) EPC.
  • FIG. 1 shows a structural drawing of a highly luminous D2R-type discharge lamp for automobile front lamp. The discharge lamp for automobiles is so arranged as that a metal iodide sealed in a quartz emissive section 5 emits a light under application of a high tension between the metal tungsten electrodes 1a and 1b. The emissive section 5 is covered with an external quartz tube 2. As compared with a halogen lamp chiefly employed at present as front lamp for automobiles, this halogen lamp is advantageous in providing a threefold luminosity at a 70% consumed power. Beside, because of using no filament unlike halogen lights, the service life is very long and not shorter than 1,500 hours.
  • In this discharge lamp, a light-screening film 4 is formed on the surface of a outer quartz tube 2 to control the project region of light. This light-screening film is about 20 µm thick, the shape and size of which are specified in according with the International Standard. The present invention refers also to a producing method for this light-screening film.
  • Using ferric oxide or cupric oxide as pigment and sodium silicate or aluminum phosphate as binder, a conventional light-screening film for lamps has been formed by mixing a pigment and a binder to form a paint, applying this paint to the glass surface of a lamp and firing the coat at a temperature of 100°C to 250°C
  • On lighting a lamp, the temperature of the glass surface of a lamp rises and accordingly that of the light-screening film formed thereon also rises. Especially with a highly luminous discharge lamp for automobiles, the temperature of the glass surface of the lamp rises to about 700°C during the lighting and necessarily the light-screening film on the glass surface is also exposed to a temperature of 700°C.
  • As mentioned above, a light-screening film according to the prior art uses ferric oxide or the like as pigment. Though being black at room temperature, cupric oxide is known to turn into red powder with the progress of oxidation at about 350°C.
  • Thus, if a light-screening film was formed on a highly luminous discharge lamp for automobiles according to the prior art, there has happened a phenomenon that the color of the light-screening film changes from black to red or white due to a rise in temperature during the lighting. When the color of the light-screening film turns from black to red or white, the absorbance of light changes, thereby leading to a decline in light-screening performance, which has given rise to troubles. Discoloration of a light-screening film leads not only to a decline in light-screening performance but a bad appearance of the lamp impressed on a user and accordingly has been a serious problem. Thus, a light-screening film material has been desired which undergoes no discoloration for a 1,500-hours period of lighting.
  • Besides, if a light-screening film was formed on a highly luminous discharge lamp for automobiles according to the prior art, there has been another problem that a heat cycle comprising ups and downs of temperature due to the repetition of lighting and extinction of a lamp causes a cracking or peeling of the light-screening film, thereby resulting in loss of light-screening performance. Also regarding this problem, a light-screening film material free of occurrence of cracking or peeling due to lighting and extinction over 1,500 hours has been desired.
  • Disclosure of the Invention
  • In order to solve these problems, the present invention employs a light-screening film paint according to claim 1 and a method according to claim 13. Preferred embodiments are disclosed in the dependent claims.
  • After a tentative drying process subsequent to the application of a paint, a paint film is formed on the glass surface by binder action of methyl cellulose, vinyl alcohol and acrylic resin. Besides, methyl cellulose functions to inhibit the sedimentation, coagulation or separation of pigment powder in a paint, whereby the paint can be stabilized by adding 0.2 to 2 parts thereof to 100 parts of powder quantity. By setting the solid fraction in the paint to not less than 40 % by weight, dry contraction or liquid dripping after the application of a paint can be suppressed, thereby enabling a high precision light-screening film pattern to be formed.
  • And preferably, by adding 0.2 to 2 parts of either silica having a primary grain size of not greater than 100 nm or clay mineral containing silica to 100 parts of powder quantity, thixotropy can be afforded to a paint, so that a stable application of the paint by using a coater becomes possible.
  • During the firing at a temperature not higher than 150°C, methyl cellulose, vinyl alcohol and acrylic resin are thermally decomposed and consequently their residue in the paint film vanishes. During the firing at a temperature not higher than 1500°C, powder glass contained in the paint melts and functions as a binder. More preferably, by using glass mainly comprising zinc oxide and silica as powder glass, a light-screening film is obtained which has a high adhesion strength to the surface of quartz glass. And more preferably, by using powder glass having a melting point of not higher than 1000°C and setting the firing temperature at not higher than 1000°C, the deterioration of lamp performance can be prevented.
  • More preferably, by using powder glass having a thermal expansion coefficient not higher than 10-6, the difference in thermal expansion coefficient from a quartz glass tube decreases and the peeling of a light-screening film due to local ups and downs of temperature caused by the lighting and extinction of a lamp hardly occurs.
  • Still more preferably, by using powder glass that will crystallize under a temperature not lower than 600°C, the deterioration of light-screening film strength due to a rise in temperature caused by the lighting of a lamp after the firing can be prevented.
  • By allowing the firing to proceed under the nitrogen atmosphere, or under the inert atmosphere, or under the vacuum atmosphere of not more than 10-2 Torr, the metal electrode material for a main lamp body is kept from being oxidized, so that a light-screening film can be formed without deterioration of the lamp performance.
  • Brief Description of the Drawings
  • FIG. 1 is an outside view of a discharge lamp;
  • FIG. 2 is an illustration of the measured results of discoloration degree for a light-screening film according to the present invention and a conventional light-screening film;
  • FIG. 3 is a table showing the mixing ratios in the mixture of manganese oxide powder and manganese-contained iron oxide powder and the estimation results of obtained light-screening films;
  • FIG. 4 is a table showing the manganese contents of manganese-contained iron oxide powder and the estimation results of obtained light-screening films;
  • FIG. 5 is a table showing the softening points of powder glass and the estimation results of obtained light-screening films;
  • FIG. 6 is a table showing the added amounts of clay mineral containing silica and the estimation results of obtained paints; and
  • FIG. 7 is a talbe showing the added amounts of methyl cellulose and the estimation results of obtained light-screening paints.
  • Detailed Description of the Preferred Embodiments
  • Next, one embodiment of the present invention will be described.
  • 100g of manganese oxide having a grain size distribution of 1µm to 20µm, 100g of iron oxide powder containing about 20 % by weight of manganese added for obtaining iron oxide from iron hydroxide and having a grain size distribution of 0.3µm to 3µm, and 100g of powder glass containing about 70 % by weight of zinc oxide, aluminum oxide and silica were dry-mixed in an agate mortar for one hour to make a mixture. The powder glass employed is one which melts at about 700°C and crystallizes as the temperature is raised up to 750°C.
  • Then, 300g of water containing 3% by weight of methyl cellulose and the above mixture were mixed in a disper mill, and the powder obtained was dispersed into water by a high-speed disperser. The mixing was performed at a surface speed of the high-speed disperser being not lower than 5m/s. The solid ratio of a paint was set to 50% by weight. And by adding one part of silica powder having a grain size of not larger than 100nm to 100 parts of powder component and dispersing it, a good thixotropy can be afforded to the coating.
  • The light-screening film paint prepared in this way was applied to the quartz glass surface of a lamp by means of a coater and fired at 800°C for an hour after transient drying at 100°C. Firing was conducted under the vacuum atmosphere of 1 x 10-4 Torr.
  • The light-screening film formed in this way on the glass surface of a highly luminous discharge lamp has a high adhesion strength to the lamp and the color of the whole film was black.
  • The light-screening film obtained was estimated by discoloration measurement after the lighting, film strength measurement, transmissibility measurement, and surface observation after the lighting.
  • And, a change in the color of a light-screening film was measured with a chroma meter and estimated in accordance with the Lab method. From changes in the respective values of L, a and b, ΔEab was calculated. The passable levels for estimation were set at a ΔEab value determined to be not greater than 1, calculated from measurements of the color of a light-screening film before lighting and after an 1,500-hours duration of lighting.
  • The film strength, determined by the cross cut test according to the JIS (Japanese Industrial Standards) Z 1522, was examined respectively before lighting and after an 1,500-hours duration of lighting. A light-screening film was cut into specimens with a diamond cutter and tapes were pasted to the respective specimens and peeled. The peeling degree of the light-screening film observed at that time was examined. Only those in which no peeling whatever was observed were determined as the passable level.
  • The passable level for transmittance measurements was taken at a leaking light ratio of not greater than 0.5%.
  • FIG. 2 shows the result of discoloration measurements of the light-screening film obtained in the above embodiment. A light-screening film according to the present invention has a much smaller degree of discoloration than that of a conventional one using cupric oxide as pigment and manifested a ΔEab value of not greater than 1 after an 1,500-hours duration of lighting.
  • In the above embodiment, 67 parts by weight of powder glass mainly containing zinc oxide was mixed to 100 parts in total of the mixture of manganese oxide powder and iron oxide powder containing about 20% by weight of manganese to prepare a paint, but light-screening films equivalent to the one obtained in the above embodiment were obtained also at other ratios.
  • FIG. 3 shows mixing ratios of the mixture of manganese oxide powder and iron oxide powder containing about 20% by weight of manganese to powder glass mainly containing zinc oxide, and the estimation results of the obtained light-screening films. This result revealed that a good light-screening film can be obtained by mixing 30 to 100 parts of powder glass mainly containing zinc oxide with 100 parts of the mixture of manganese oxide powder and manganese-contained iron oxide powder.
  • In the above embodiment, the manganese content in manganese-contained iron oxide was 20%, but results similar to the one obtained in the above embodiment were obtained also at other ratios. FIG. 4 shows these results. From FIG. 4 the most appropriate content of manganese was found to range from 5 mol% to 30 mol%.
  • In the above embodiment, powder glass mainly containing zinc oxide was employed, but powder glass mainly comprising any of zinc oxide or boron oxide or aluminum oxide or silica provided a light-screening film equivalent to the one obtained in the above embodiment.
  • On using powder glass containing a great amount of alkaline metal or alkaline earth metal, no good result was obtained because it reacted to cause an external quartz glass tube to be devitrifed.
  • In the above embodiment, powder glass that begins to melt at 700°C and is crystallized at 750°C was employed, but a light-screening films equivalent to the one obtained in the above embodiment were obtained for powder glass having other softening points. FIG. 5 shows these results. To allow glass to melt sufficiently, the firing temperature was set to the softening temperature plus 100°C. From FIG. 5 it proved appropriate that the melting point of the powder glass employed ranges from 600°C to 1,100°C, both inclusive, and the firing temperature is not higher than 1,200°C.
  • And with respect to adhesion strength of a film, using glass to be crystallized with elevating temperature provides a rather preferred result.
  • In the above embodiment, thixocity was afforded to a paint by adding one part of silica powder having a grain size of not greater than 100nm to 100 parts of powder quantity, but equivalent results were obtained also on using swelling clay minerals such as smectite containing silica in place of silica powder. The powder quantity referred to here is the total quantity of a mixture comprising manganese oxide and manganese contained iron oxide and powder glass.
  • Silica powder having a larger grain size that 100nm provides no desired effect.
  • A most appropriate added amount of silica powder depends on a coater or a desired thickness, but the results examined in the present invention are shown in FIG. 6. FIG. 6 revealed that 0.2 part to 2 parts of added amount to 100 parts of powder quantity is suitable for the attainment of a stable coating by the prevention of liquid dripping or the like. FIG. 6 shows the results examined on swelling clay minerals containing silica, but equivalent results were obtained also for silica powder having a grain size of not greater than 100nm.
  • In the above embodiment, methyl cellulose was employed, but equivalent paints were obtained also on using vinyl alcohol or acrylic resin in place of this.
  • FIG. 7 shows the results of correspondence between the added amount of methyl cellulose. The results of FIG. 7 revealed that the added amount of methyl cellulose is preferably 0.2 to 2 parts to 100 parts of powder quantity. FIG. 7 shows the results in the case of methyl cellulose, but equivalent results were obtained also on using vinyl alcohol or acrylic resin in place of this.
  • In the above embodiment, firing was conducted in the atmosphere of 1 x 10-4 Torr. As a result of examinations on the degree of vacuum, firing in the vacuum atmosphere of not lower than 1 x 10-2 Torr provided no favorable result because the tungsten electrode section of the lamp of FIG. 1 was oxidized. Thus, the degree of vacuum was found to be preferably not higher than 1 x 10-2 Torr.
  • According to the present invention, as described above, a favorable effect in a light-screening film formed on the glass surface of a highly luminous discharge lamp was obtained that the adhesion strength to a lamp is strong, the color of the whole film is black and neither peeling nor discoloration of the light-screening film occurs even after a 200-hours duration of lighting.

Claims (24)

  1. A light-screening film paint for lamps comprising:
    at least one compound of either manganese oxide or iron oxide; and
    powder glass containing at least one of compounds respectively of silica, zinc oxide, boron oxide and aluminum oxide,
    characterized in that
    said compound contains 5 mol% to 30 mol% of manganese.
  2. A light-screening film paint for lamps as set forth in claim 1,
    characterized by
    a compound of manganese oxide, iron oxide and zinc oxide; and
    glass containing at least one compound respectively of silica, zinc oxide, boron oxide, and aluminum oxide.
  3. A light-screening film paint for lamps as set forth in claim 1, wherein water is employed as solvent.
  4. A light-screening film paint for lamps as set forth in claim 1, further comprising at least one of compounds respectively of methyl cellulose, vinyl alcohol, and acrylic resin.
  5. A light-screening film paint for lamps as set forth in claim 1, wherein silica having a primary grain size of not greater than 100 nm is added.
  6. A light-screening film paint for lamps as set forth in claim 1, wherein clay mineral containing silica having a primary grain size of not greater than 100 nm is added.
  7. A light-screening film paint for lamps as set forth in claim 1, wherein the solid fraction is not smaller than 40 % by weight.
  8. A light-screening film paint for lamps as set forth in claim 1, wherein the melting point of powder glass is not higher than 1,200°C.
  9. A light-screening film paint for lamps as set forth in claim 4, wherein the amount of the compound of at least one of methyl cellulose, vinyl alcohol and acrylic resin ranges from 0.2 part to 2 parts relative to 100 parts of powder quantity.
  10. A light-screening film paint for lamps as set forth in claim 1, wherein the thermal expansion coefficient of the powder glass is not higher than 10-6.
  11. A light-screening film paint for lamps as set forth in claim 1, wherein the powdered glass to be crystallized by heating is employed as powder glass for preparing said light-screening film paint.
  12. A light-screening film paint for lamps as set forth in claim 1, wherein relative to 100 parts of at least one compound of either manganese oxide or iron oxide containing 5 mol% to 30 mol% of manganese, the mixing ratio of said powder glass containing at lest one of the compounds respectively of silica, zinc oxide, boron oxide, and aluminum oxide ranges from 30 parts by weight to 100 parts by weight.
  13. A method for producing a light-screening film (4) for lamps, comprising the steps of:
    preparing a light-screening paint for lamps; said light-screening paint comprises at least one compound of either manganese oxide or iron oxide and moreover powder glass containing at least one compound, respectively, of silica, zinc oxide, boron oxide and aluminum oxide.
    applying the above paint to the surface of a lamp,
    forming a light-screening film (4) by firing at not higher temperatures than 1200°C,
    characterized in that
    said compound contains 5 mol% to 30 mol% of manganese.
  14. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein water is employed as solvent.
  15. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein added to said light-screening film paint is a compound of at least one of methyl cellulose, vinyl alcohol and acrylic resin.
  16. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein silica having a primary grain size of not greater than 100 nm is added.
  17. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein clay mineral containing silica having a primary grain size of not greater than 100 nm is added.
  18. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein the solid fraction is not smaller than 40 % by weight.
  19. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein the melting point of powder glass is not higher than 1,200°C.
  20. A producing method of a light-screening film 4 for lamps as set forth in claim 15, wherein the amount of the compound of at least one of methyl cellulose, vinyl alcohol and acrylic resin ranges from 0.2 part to 2 parts relative to 100 parts of powder quantity.
  21. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein the firing of said paint is allowed to proceed in the vacuum atmosphere of not more than 10-2 Torr.
  22. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein the thermal expansion coefficient of the powder glass is not higher than 10-6.
  23. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein the powder glass to be crystallized by heating is employed as powder glass for preparing said light-screening film paint.
  24. A producing method of a light-screening film 4 for lamps as set forth in claim 13, wherein relative to 100 parts of at least one compound of either manganese oxide or iron oxide containing 5 mol% to 30 mol% of manganese, the mixing ration of said powder glass containing at least one of the compounds respectively of silica, zinc oxide, boron oxide and aluminum oxide ranges from 30 parts by weight to 100 parts by weight.
EP97104628A 1996-03-19 1997-03-18 Light-screening film paint for lamps, and light-screening film for lamps and producing method thereof Expired - Lifetime EP0797238B1 (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP62366/96 1996-03-19
JP06236696A JP3444086B2 (en) 1996-03-19 1996-03-19 Paint, light-shielding film for lamp using the same, and method of manufacturing the same
JP6236696 1996-03-19
JP8305405A JPH10147736A (en) 1996-11-18 1996-11-18 Paint for light-shielding film, lamp with light-shielding film, and method of manufacturing the same
JP305405/96 1996-11-18
JP30540596 1996-11-18

Publications (3)

Publication Number Publication Date
EP0797238A2 EP0797238A2 (en) 1997-09-24
EP0797238A3 EP0797238A3 (en) 1997-12-10
EP0797238B1 true EP0797238B1 (en) 2001-10-17

Family

ID=26403421

Family Applications (1)

Application Number Title Priority Date Filing Date
EP97104628A Expired - Lifetime EP0797238B1 (en) 1996-03-19 1997-03-18 Light-screening film paint for lamps, and light-screening film for lamps and producing method thereof

Country Status (3)

Country Link
EP (1) EP0797238B1 (en)
CN (1) CN1101433C (en)
DE (1) DE69707332T2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000001338A (en) 1998-06-15 2000-01-07 Matsushita Electric Ind Co Ltd Light shielding film for discharge lamp and method of manufacturing the same

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL6918887A (en) * 1969-12-17 1971-06-21
DE2136012A1 (en) * 1971-07-19 1973-02-01 Patra Patent Treuhand ELECTRIC LAMP WITH LIGHT COVERING COVER
DD102010A1 (en) * 1973-01-15 1973-11-20
US4288713A (en) * 1979-11-23 1981-09-08 Gte Products Corporation Lamp having opaque coating
JP2761155B2 (en) * 1992-07-08 1998-06-04 株式会社小糸製作所 Discharge lamp device for light source of automotive lamp
EP0739534B1 (en) * 1994-11-10 1998-07-15 Koninklijke Philips Electronics N.V. Electric lamp

Also Published As

Publication number Publication date
CN1101433C (en) 2003-02-12
DE69707332D1 (en) 2001-11-22
CN1163292A (en) 1997-10-29
DE69707332T2 (en) 2002-05-02
EP0797238A3 (en) 1997-12-10
EP0797238A2 (en) 1997-09-24

Similar Documents

Publication Publication Date Title
EP0585830B2 (en) Lead-free glass coatings
US5827789A (en) Lead-free glass composition and the use thereof
US5089172A (en) Thick film conductor compositions for use with an aluminum nitride substrate
JP3898779B2 (en) Lead-free glass frit, ceramic enamel composition containing the same, and enameled glass substrate
CN111788166B (en) Overglaze decorative material, ceramic product, method for manufacturing ceramic product
JPS6238305B2 (en)
US5629247A (en) High bismuth oxide based flux and paint compositions for glass substrates
CZ298760B6 (en) Enamel composition, process for enameling glass substrates with such composition and products obtainedEnamel composition, process for enameling glass substrates with such composition and products obtained
US6015592A (en) Light-screening film paint for lamps, and light-screening film for lamps and producing method thereof
GB1559589A (en) Discharge lamp envelopes
KR910006945B1 (en) High Temperature Antioxidant Paint for Electrode
EP0797238B1 (en) Light-screening film paint for lamps, and light-screening film for lamps and producing method thereof
US5296414A (en) Partially crystallizable low melting glass
US5504045A (en) Paint composition
US5362687A (en) Lead-free frit glaze
KR20220021464A (en) Tinted glass frits and related methods for automotive applications
KR100365292B1 (en) Glass Composition and Fluorescent Lamp for Phosphor Bonding
US4012655A (en) Refractory metal oxide reflector coating on lamp envelope
US5013362A (en) Fluorine-free superopaque enamel frits
JP2000226232A (en) Leadless low-melting glass composition
HK1003342A1 (en) Process for the preparation of decorations color-stabilized during sintering porcelain and pigment composition suitable therefor
JP2001089187A (en) Glass composition for dielectric substance of plasma display panel
DE4345516C2 (en) Glaze compound for coating ceramic substrate
JPS6121582B2 (en)
KR20070103986A (en) High Brightness Dielectric Glass for Display

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): DE FR GB NL

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): DE FR GB NL

17P Request for examination filed

Effective date: 19980226

17Q First examination report despatched

Effective date: 19990729

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB NL

REF Corresponds to:

Ref document number: 69707332

Country of ref document: DE

Date of ref document: 20011122

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20060308

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20060315

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20060316

Year of fee payment: 10

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20070318

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20071001

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20071130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20071001

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20071002

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20070318

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20070402

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20060315

Year of fee payment: 10