WO2008018682A1 - composition de pâte pour couche diélectrique d'écran d'affichage plasma, écran d'affichage plasma utilisant la composition de pâte, et son procédé de fabrication - Google Patents

composition de pâte pour couche diélectrique d'écran d'affichage plasma, écran d'affichage plasma utilisant la composition de pâte, et son procédé de fabrication Download PDF

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Publication number
WO2008018682A1
WO2008018682A1 PCT/KR2007/002817 KR2007002817W WO2008018682A1 WO 2008018682 A1 WO2008018682 A1 WO 2008018682A1 KR 2007002817 W KR2007002817 W KR 2007002817W WO 2008018682 A1 WO2008018682 A1 WO 2008018682A1
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WO
WIPO (PCT)
Prior art keywords
weight
parts
paste composition
oxide
display panel
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Application number
PCT/KR2007/002817
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English (en)
Inventor
Gyung Soo Kim
Yong Hyun Kim
Mun Hyuk Lim
Original Assignee
Lg Electronics Inc.
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
Application filed by Lg Electronics Inc. filed Critical Lg Electronics Inc.
Publication of WO2008018682A1 publication Critical patent/WO2008018682A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/24—Fusion seal compositions being frit compositions having non-frit additions, i.e. for use as seals between dissimilar materials, e.g. glass and metal; Glass solders
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00—Glass compositions
    • C03C3/04—Glass compositions containing silica
    • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00—Glass compositions
    • C03C3/04—Glass compositions containing silica
    • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/078—Glass compositions containing silica with 40% to 90% silica, by weight containing an oxide of a divalent metal, e.g. an oxide of zinc
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00—Glass compositions
    • C03C3/04—Glass compositions containing silica
    • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00—Glass compositions
    • C03C3/04—Glass compositions containing silica
    • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
    • C03C3/093—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium

Definitions

  • the present invention relates to a photosensitive paste composition for a dielectric layer, a plasma display panel using the composition, and a method of manufacturing the panel. [10]
  • Plasma display panel is a flat panel display device that can display images or information by using a light-emitting phenomenon from plasma discharge.
  • PDP is generally divided into DC-type and AC-type according to panel structure and driving method.
  • PDP generates plasma discharge in each cell separated by barrier ribs.
  • PDP is a display device using the light emitting phenomenon of visible rays generated from the energy difference when ultraviolet rays generated by plasma discharge of a gas (such as He, Xe, etc.) provided in each cell returns to the ground state by exciting a phosphor in the cell.
  • a gas such as He, Xe, etc.
  • PDP has several advantages such as simple structure, easy manufacturing due to simple structure, high brightness, high luminous efficacy, high memory capacity, and a wide viewing angle over 160°. Also, PDP can be used for wide screens of 40 or more inches.
  • PDP includes a front substrate and a rear substrate opposed to each other, and a barrier rib.
  • the front substrate, the rear substrate and the barrier rib divide cells.
  • a transparent electrode is disposed on the front substrate, and a bus electrode is disposed on the transparent electrode for decreasing resistance of the transparent electrode.
  • An address electrode is disposed on the rear substrate.
  • a phosphor material is applied inside of the cells divided by the barrier ribs.
  • a front dielectric layer is formed to cover the transparent electrode and the bus electrode on the front substrate.
  • a rear dielectric layer is disposed on the rear substrate to cover the address electrode.
  • a protection layer is made of MgO, and disposed on the front dielectric layer.
  • a general method of manufacturing the dielectric layer, especially the rear dielectric layer is as follows. [19] First, a paste composition having a glass powder, a solvent and a binder is printed on the rear substrate with the address electrode.
  • the paste composition is dried at 150 0 C for 5 to 10 minutes.
  • the dried paste composition is sintered to form the rear dielectric layer.
  • Fig. 1 is a perspective view illustrating the PDP according to one embodiment of the present invention
  • Figs. 2 - 5 are cross-sectional views illustrating the steps of forming the rear dielectric layer according to one embodiment of the present invention
  • Fig. 6 is a view illustrating cross-sections of the rear dielectric layers formed by using each of the paste compositions in trial tests.
  • One object of the present invention is to provide a paste composition for a dielectric layer formed by using a UV cured type of paste composition, whereby the process can be simplified, the manufacturing cost can be reduced, and the productivity can be improved; and a plasma display panel (PDP) using the paste composition; and a method of manufacturing the PDP.
  • Another object of the present invention is to provide a PDP having an eco-friendly dielectric layer in the process of which the power consumption is low by using a paste composition not having a solvent, and a method of manufacturing the PDP.
  • Fig. 1 is a perspective view illustrating the PDP according to one embodiment of the present invention.
  • Fig. 1 the structure of PDP is divided into a front plate 200 and a rear plate 300.
  • transparent electrodes 220, bus electrodes 230, a front dielectric layer 240, and a protection layer 250 are formed on a lower side of a glass substrate 210 (hereinafter, referred to as "front substrate”).
  • the transparent electrodes 220 are formed with indium tin oxide (hereinafter, referred to as "ITO") to transmit a light from a discharging cell.
  • ITO indium tin oxide
  • the bus electrodes 230 are disposed on the transparent electrodes 220 to decrease line resistance of the transparent electrodes 220.
  • the bus electrodes 230 are made of a material, like silver (Ag) paste, having high conductivity.
  • the bus electrodes 230 can decrease the driving voltage of the transparent electrodes 220 having low conductivity because the bus electrodes 230 are made of a material having high conductivity.
  • the front dielectric layer 240 directly contacts with the bus electrodes 230 made of metallic material, and may be made of PbO-based glass or non-Pb-based glass in order to avoid chemical reactions with the bus electrodes 230. This front dielectric layer 240 restricts discharge current to maintain glow discharge, and the electric charges generated at the time of plasma discharge are accumulated.
  • the protection layer 250 prevents damage of the front dielectric layer 240 by sputtering at the time of plasma discharge, and increases the discharge efficiency of the secondary electrons as well.
  • the protection layer 250 is made up of magnesium oxide
  • address electrodes 320 In the rear plate 300 of PDP, address electrodes 320, a rear dielectric layer 330, barrier ribs 340, and a phosphor layer 350 are disposed on the upper surface of a glass substrate 310 (hereinafter, referred to as "rear substrate").
  • the address electrodes 320 are positioned in the middle of each discharge cell.
  • the address electrodes 320 may have a line width of about 70 to 80 D .
  • the rear dielectric layer 330 is disposed on the entire surface of the rear substrate 310 and the address electrodes 320, and protects the address electrodes 320.
  • the barrier ribs 340 are positioned on top of the rear dielectric layer 330, spaced by a predetermined distance from the address electrodes 320, and are formed longer in the perpendicular direction. [49]
  • the barrier ribs 340 may have variety type, for example, a stripe type, a well type, a delta type or a honeycomb type.
  • the barrier ribs 340 are needed to maintain a discharge distance, and prevent electrical and optical interference between adjacent discharge cells.
  • the phosphor layer 350 is formed over both sides of the barrier ribs 340 and the upper surface of the rear dielectric layer 330.
  • the phosphor layer 350 is excited by the ultraviolet rays generated at the time of plasma discharge, and generates a red (R), green (G) or blue (B) visible ray.
  • the electrons to which the force is exerted obtain an energy (first ionization energy) enough to remove electrons in the outermost orbit, they ionize the gas, and thus generated ions and electrons are moved to both electrodes by the electromagnetic force. Particularly, secondary electrons are generated when the ions collide with the protection layer 250, and these secondary electrons help generation of plasma.
  • the gas provided into the cells of PDP is generally an inert gas, such as Ne, Xe, He, etc.
  • a red, green or blue visible ray is generated when an ultraviolet ray with a wavelength of between about 147 nm and 173 nm is applied to the phosphor layer 350.
  • each discharge cell becomes a pixel representing each red, green, or blue color.
  • each discharge cell is controlled by combination of RGB in each discharge cell.
  • the color is controlled by controlling the time during which plasma is generated.
  • Figs. 2 - 5 are cross-sectional views illustrating the steps of forming the rear dielectric layer according to one embodiment of the present invention.
  • a paste composition 332 is applied onto the rear substrate
  • a dielectric forming layer 334 is formed as shown in Fig. 3.
  • the dielectric forming layer 334 becomes the rear dielectric layer 330 by sintering.
  • the paste composition 332 comprises a glass powder, a photosensitive monomer, a photosensitive oligomer, a photo initiator, a dispenser and a thixotrophic agent.
  • the paste composition 332 comprises about 50 to 70 parts by weight of the glass powder, about 10 to 30 parts by weight of the filler, about 10 to 30 parts by weight of the photosensitive monomer, about 1 to 10 parts by weight of the photosensitive oligomer, about 0.5 to 5 parts by weight of the photo initiator, and about 0.5 to 5 parts by weight of the dispenser.
  • the glass powder is at least one selected from the group consisting of a silicon dioxide, a lead oxide, a zinc oxide, a bismuth oxide and a boron oxide, as main components.
  • the glass powder can be functioned as supporter of the rear dielectric layer 330.
  • the filler is at least one selected from the group consisting of a barium oxide, a calcium oxide, a magnesium oxide, a zinc oxide, a zirconium oxide, a titanium oxide and an aluminum oxide, in the amount of about 2 to 30 parts by weight.
  • the filler plays a role to increase the reflectivity and strength of the rear dielectric layer 330.
  • the photo initiator plays a role to increase photo-sensitivity in case the exposing process is conducted onto the paste composition 332.
  • the photo initiator is at least one selected from a reducing agent group consisting of benzophenone, benzoyl benzoic acid methyl, 4,4-bis(dimethylamine)benzophenone, 4,4-bis(diethylamine)benzophenone, 4,4-dichlorobenzophnone, 4-benzoyl-4-methyldiphenylketone, dibenzilketone, fluorenon, 2,2-diethoxyacetophenone, 2,2-dimethoxy-2-phenyl-2-phenylacetophenone, 2-hydroxy-2-methylpropiophenone, p-t-buthyldichloroacetophenone, thioxanthone, 2-methylthioxanthone, 2-chlorothioxanthone, 2-isopropylthioxanthone, diethylth- ioxanthone, benzyl,
  • the photo initiator can be used by about 0.5 to 5 parts by weight, preferably 0.5 to 2 parts by weight. If the amount of photo initiator is too little, the photo sensitivity is not good. If the amount of photo initiator is too much, the survival rate of exposing part may be too low.
  • the dispenser plays a role to dispense the glass powder equally in the paste composition 332.
  • the dispenser can be at least one selected from the group consisting of polyamineamide based compound, polycarboxylic acid based high molecular compound, fish oil, polyethyleneglycolether, alkylsulfonate, poly carboxy late, alky- lammonium, silicon, or acryl based dispenser; and can be used alone or in mixture of two or more.
  • the silicon based dispenser can be amino triethoxy silane, amino trimethoxy silane, octadecyltriethoxy silane, octadecyltrimethoxy silane, etc.
  • the acryl based dispenser is high or low molecular based acryl dispenser.
  • the amount of dispenser in the present paste composition 332 is about 0.5 to 5 parts by weight, preferably about 0.5 to 2 parts by weight.
  • the thixotrophic agent plays a role to increase viscosity of the paste composition
  • the present paste composition 332 may not comprise a solvent, and so can form an eco-friendly dielectric layer.
  • the photosensitive monomer is acrylic based monomer that is at least one selected from the group consisting of methylacrylate, ethylacrylate, n-propylacrylate, isopropy- lacrylate, n-butylacrylate, sec-butylacrylate, iso-butylacrylate, tert-butylacrylate, n- pentylacrylate, allylacrylate, benzilacrylate, butoxyethylacrylate, butoxytriethylenegly- colacrylate, cyclohexylacrylate, dicyclopentanylacrylate, dicyclopentenylacrylate, 2-ethylhexylacrylate, glycerolacrylate, glycidylacrylate, heptadecafluorodecylacrylate, 2-hydroxyethylacrylate, isobonylacrylate, 2-hydroxypropylacrylate, isothexylacrylate, isooctylacrylate, lau
  • the photosensitive monomer is an aromatic monomer substituted with 1 to 5 chlorine or fluorine atoms.
  • At least one acrylate can be substituted with methacrylate.
  • the photosensitive monomer is isobonyl acrylate or isobonyl methacrylate.
  • the photosensitive monomer is vinyl based monomer that is at least one selected from the group consisting of styrene, p-methylstyrene, o-methylstyrene, m- methylstyrene, chlorinated styrene, brominated styrene, alpha-methylstyrene, chlorinated alpha-methylstyrene, brominated alpha-methylstyrene, chloromethylstyrene, hydroxymethylstyrene, carboxymethylstyrene, vinylnaphthalene, vinylanthracene, vinylcarbazole and l-vinyl-2-pyrolidone.
  • the photosensitive oligomer is at least one selected from the group consisting of melamine acrylate, epoxy acrylate, urethane acrylate, polyester acrylate, polyethylene glycol bisacrylate having the molecular weight of 500 to 3000, and polypropylene glycol bismethaacrylate having the molecular weight of 500 to 3000.
  • the photosensitive oligomer is urethane acrylate.
  • the dielectric forming layer 334 is exposed for a certain period of time, as shown in
  • Exposure devices such as stepper exposer or proximity exposer may be used. For light exposure on a large area, the exposure is conducted by applying a paste or an electrode material over a glass or other substrate for return, whereby an exposer for small area can be used for large area.
  • the active light sources that can be used at that time include visible light, near ultraviolet light, ultraviolet light, electron beam, X-ray, and laser beam, preferably ultraviolet light.
  • the sources low-pressure mercury lamp, high-pressure mercury lamp, extra-high pressure mercury lamp, halogen lamp, and germicidal lamp can be used, but the extra-high pressure mercury lamp is preferred.
  • the paste composition 332 is cured to form the dielectric forming layer 334.
  • the cured dielectric forming layer 334 is sintered at a certain temperature for forming the rear dielectric layer 330, as shown in Fig. 5.
  • the trial test results to the rear dielectric layer which is formed by using the paste composition for dielectric layer according to the above embodiment will be described.
  • Comparative Example 1 formed a rear dielectric layer by using the paste composition comprising about 60 parts by weight of glass powder, 4 parts by weight of Al 2 O 3 , 11 parts by weight of TiO , 3 parts by weight of binder, and 22 parts by weight of solvent.
  • binder EC STD 4 and EC STD 20 produced by Dow Chemical Co. were used by 1 and 2 parts by weight, respectively.
  • solvent ⁇ -Terpineol was used by about 15 parts by weight, and BCA was used by about 7 parts by weight.
  • Comparative Example 1 The past composition of Comparative Example 1 was applied on the rear substrate, dried, and sintered to form the rear dielectric layer. [95] In Examples 1 to 3, the photosensitive monomer was IBXA (Isobonyl Acrylaye),
  • urethane based oligomer such as EB230 and EB9270 produced by SKCYTEC Co. was used.
  • IR907, IR819 and TPO were used as the photo initiator; BYK180 of BYK Co. was used as the dispenser; and BYK410 of BYK Co. was used as the thixotrophic agent.
  • the paste composition of Example 1 comprises about 60 parts by weight of glass powder, about 4 parts by weight of Al O , about 11 parts by weight of TiO , about 17 parts by weight of photosensitive monomer, about 6 parts by weight of photosensitive oligomer, about 1 part by weight of photo initiator, and about 1 part by weight of dispenser.
  • EB9270 was used; and as the photo initiator, TPO was used.
  • the paste composition of Example 2 comprises about 60 parts by weight of glass powder, about 4 parts by weight of Al O , about 11 parts by weight of TiO , about 20 parts by weight of photosensitive monomer, about 4 parts by weight of photosensitive oligomer, about 1 part by weight of photo initiator, about 0.9 part by weight of dispenser and about 0.01 part by weight of thixotrophic agent.
  • photosensitive monomer IBXMA was used; as the photosensitive oligomer, about 1 part by weight of EB230 and about 3 parts by weight of EB 9270 were used; and as the photo initiator, about 0.6 part by weight of IR907 and about 0.4 part by weight of TPO were used.
  • the paste composition of Example 3 comprises about 60 parts by weight of glass powder, about 4 parts by weight of Al O , about 11 parts by weight of TiO , about 20 parts by weight of photosensitive monomer, about 8 parts by weight of photosensitive oligomer, about 1 part by weight of photo initiator and about 1 part by weight of dispenser.
  • photosensitive monomer about 10 parts by weight of IBXA, about 5 parts by weight of 4-HBA and about 5 parts by weight of IBXMA were used.
  • photosensitive oligomer about 5 parts by weight of EB230 and about 3 parts by weight of EB9270 were used.
  • photo initiator about 0.3 part by weight of IR819 and about 0.7 part by weight of TPO were used.
  • the trial test according to the present invention first, evaluated the characteristics of viscosity and printing of the paste compositions of Comparative Example 1, and Examples 1 to 3. [105] Then, to the rear dielectric layer formed by each of the paste compositions, sintering intensity of surface illumination, reflectivity, and withstanding voltage were tested, and the test results are shown in Table 2 below.
  • Fig. 6 is a view illustrating cross-sections of the rear dielectric layers formed by each of the paste compositions used in trial tests.
  • the reflectivity is a rate of reflecting light incident to the rear dielectric layer. If the reflectivity is more than 50%, it is acceptable. In the trial tests, Comparative Example 1, and Examples 1 to 3 showed satisfactory levels of reflectivity.
  • Comparative Example 1 manufactured by conventional method Examples 1 to 3 manufactured according to the present invention showed satisfying results compared with the characteristics of the prior rear dielectric layer as a whole, without the dry process in the art.
  • the present invention has advantages that the power consumption is less compared with the prior art; the eco-friendly dielectric layer can be manufactured by using the paste composition not having a solvent; and the manufacturing time can be reduced since the curing can be done within a short period of time, with maintaining the normal characteristics in the art.
  • An embodiment may be achieved in whole or in part by the paste composition for a dielectric layer comprising about 50 to 70 parts by weight of a glass powder, about 10 to 30 parts by weight of a filler, about 10 to 30 parts by weight of a photosensitive monomer, about 1 to 10 parts by weight of a photosensitive oligomer, about 0.5 to 5 parts by weight of a photo initiator and about 0.5 to 5 parts by weight of a dispenser.
  • any reference in the present specification to "one embodiment,” “an embodiment,” “example embodiment,” etc. means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the invention.
  • the appearances of such phrases in various places in the specification are not necessarily all referring to same embodiment.

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  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Geochemistry & Mineralogy (AREA)
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Abstract

La présente invention concerne une composition de pâte pour couche diélectrique, un écran d'affichage plasma utilisant la composition de pâte, et un procédé de fabrication dudit écran. L'écran d'affichage plasma comprend un substrat inférieur et un substrat supérieur opposés l'un à l'autre, des électrodes d'adresse formées sur le substrat inférieur, des électrodes de décharge formées sur le substrat supérieur, des couches diélectriques inférieure et supérieure disposées sur chacune des électrodes d'adresse et des électrodes de décharge, une nervure de protection disposée entre le substrat inférieur et le substrat supérieur et divisant une pluralité de cellules de décharge, et une couche de fluorescence formée dans les cellules de décharge divisée par une nervure de protection. La composition de pâte pour couche diélectrique comprend environ 50 à 70 parties en poids d'une poudre de verre, environ 10 à 30 parties en poids d'une matière de remplissage, environ 10 à 30 parties en poids d'un monomère photosensible, environ 1 à 10 parties en poids d'un oligomère photosensible, environ 0,5 à 5 parties en poids d'un photo-initiateur, et environ 0,5 à 5 parties en poids d'un distributeur. La composition de pâte et l'écran d'affichage plasma utilisant ladite composition selon la présente invention présente des avantages en ce sens que le processus de fabrication est plus simple, le coût de fabrication est moindre, et la productivité plus élevée, grâce à un type de vulcanisation UV de composition de pâte, par rapport à l'art antérieur.
PCT/KR2007/002817 2006-08-08 2007-06-12 composition de pâte pour couche diélectrique d'écran d'affichage plasma, écran d'affichage plasma utilisant la composition de pâte, et son procédé de fabrication WO2008018682A1 (fr)

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Application Number Priority Date Filing Date Title
KR10-2006-0074601 2006-08-08
KR1020060074601A KR100800463B1 (ko) 2006-08-08 2006-08-08 유전체층용 페이스트 조성물, 이를 이용한 플라즈마디스플레이 패널 및 그 제조방법

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Cited By (5)

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JP2010117702A (ja) * 2008-10-17 2010-05-27 Taiyo Ink Mfg Ltd ソルダーレジスト組成物及びこれを用いて形成するプリント配線板
JP2010117703A (ja) * 2008-10-17 2010-05-27 Taiyo Ink Mfg Ltd 硬化性樹脂組成物及び反射シート
JP2012137769A (ja) * 2012-02-06 2012-07-19 Taiyo Holdings Co Ltd ソルダーレジスト組成物およびプリント配線板
CN101962515B (zh) * 2009-07-22 2012-08-08 东莞市贝特利新材料有限公司 硅橡胶与塑料粘接的紫外光固化胶粘剂
WO2023063654A1 (fr) * 2021-10-12 2023-04-20 아이원스 주식회사 Verre résistant au plasma, composant de chambre interne pour procédé de fabrication de semi-conducteur et leurs procédés de fabrication

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KR20060086776A (ko) * 2005-01-27 2006-08-01 엘지전자 주식회사 플라즈마 디스플레이 패널의 격벽 제조 방법

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US6043604A (en) * 1996-07-10 2000-03-28 Toray Industries, Inc. Plasma display with barrier rib of specific construction
JPH11335138A (ja) * 1998-03-10 1999-12-07 Toray Ind Inc 感光性ペ―スト、プラズマディスプレイ、およびプラズマアドレス液晶ディスプレイならびにそれらの製造方法
JPH11323147A (ja) * 1998-05-18 1999-11-26 Toray Ind Inc 誘電体ペーストおよびそれを用いたディスプレイ基板の製造方法
US20040198131A1 (en) * 1999-03-25 2004-10-07 3M Innovative Properties Company Method of producing substrate for plasma display panel and mold used in the method
KR20060055638A (ko) * 2004-11-18 2006-05-24 신유선 디스플레이 장치용 격벽 조성물 및 이를 이용한 격벽제조방법

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010117702A (ja) * 2008-10-17 2010-05-27 Taiyo Ink Mfg Ltd ソルダーレジスト組成物及びこれを用いて形成するプリント配線板
JP2010117703A (ja) * 2008-10-17 2010-05-27 Taiyo Ink Mfg Ltd 硬化性樹脂組成物及び反射シート
JP2012128442A (ja) * 2008-10-17 2012-07-05 Taiyo Holdings Co Ltd ソルダーレジスト組成物及びプリント配線板
CN101962515B (zh) * 2009-07-22 2012-08-08 东莞市贝特利新材料有限公司 硅橡胶与塑料粘接的紫外光固化胶粘剂
JP2012137769A (ja) * 2012-02-06 2012-07-19 Taiyo Holdings Co Ltd ソルダーレジスト組成物およびプリント配線板
WO2023063654A1 (fr) * 2021-10-12 2023-04-20 아이원스 주식회사 Verre résistant au plasma, composant de chambre interne pour procédé de fabrication de semi-conducteur et leurs procédés de fabrication

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