US20070190429A1 - Composition for inkjet spacer formation and spacer element using the same - Google Patents

Composition for inkjet spacer formation and spacer element using the same Download PDF

Info

Publication number
US20070190429A1
US20070190429A1 US11/671,300 US67130007A US2007190429A1 US 20070190429 A1 US20070190429 A1 US 20070190429A1 US 67130007 A US67130007 A US 67130007A US 2007190429 A1 US2007190429 A1 US 2007190429A1
Authority
US
United States
Prior art keywords
weight
parts
acetate
spacer
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/671,300
Inventor
Joon-Hyung Kim
Young-Sun Kong
Kyung-Jun Kim
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.)
LG Chem Ltd
Original Assignee
LG Chem 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
Application filed by LG Chem Ltd filed Critical LG Chem Ltd
Priority to US11/671,300 priority Critical patent/US20070190429A1/en
Publication of US20070190429A1 publication Critical patent/US20070190429A1/en
Assigned to LG CHEM, LTD. reassignment LG CHEM, LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KIM, JOON-HYUNG, KIM, KYUNG-JUN, KONG, YOUNG-SUN
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/023Emulsion inks
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00Inks
    • C09D11/30Inkjet printing inks
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials

Definitions

  • the present invention relates to a composition for spacer formation used for color televisions, computer monitors, and other display devices, and a spacer element using the same.
  • a liquid crystal display is manufactured by forming a liquid crystal driving device, such as a TFT (thin film transistor), and a coloring device, such as a color filter, on a pair of opposing transparent insulating substrates. Between the substrates there are spacers that maintains a 3 to 10 ⁇ m space therebetween. Liquid crystal is injected in this space, and then the spacing is sealed to form a liquid crystal device.
  • a liquid crystal driving device such as a TFT (thin film transistor)
  • a coloring device such as a color filter
  • the spacer Conventionally, spherical or cylindrical silica, alumina, or synthetic resin particles randomly distributed between the TFT substrate and the color filter substrate have been used as the spacer. But, in this case, the spacer around the light passage of the liquid crystal display may hinder driving of the liquid crystal or deteriorate the display quality due to the optical properties of the spacer itself.
  • the spacer formation process requires many steps including spin coating, pre-baking, exposure, developing, and post-baking of the spacer substance, and therefore the manufacturing cost increases.
  • Korea Patent Publication No. 2001-0049941, Japan Patent Publication No. 2001-109002, and Japan Patent Publication No. 2001-83525 proposed a method for selectively forming a spacer on the black matrix through which no light passes, by the inkjet process.
  • Korea Patent Publication No. 2001-0049941 and Japan Patent Publication No. 2001-83525 proposed a cross-linking spacer-forming substance, which could be sprayed by the inkjet head, and which used a homopolymer or copolymer as a cross-linkable substance. Usage of the substance was limited from 0.01 to 30 parts by weight.
  • the sprayed solvent is evaporated in the cross-linking step, and only the homopolymer or copolymer forms the spacer.
  • the diameter of the ink droplet on the substrate surface remains almost the same due to its adhesivity, its height decreases, so that the height of the final spacer becomes significantly lower than that of the ink droplet. Accordingly, the height becomes insufficient for a high-resolution black matrix, which requires a small diameter.
  • Japan Patent Publication No. 2001-109002 proposed that it is preferable to use a monomer or oligomer with a low molecular weight, considering the spraying characteristics of the ink, while limiting the content of the solvent under 50 parts by weight and increasing the content of the spacer-forming substance.
  • a substance with a low molecular weight does not have sufficient mechanical properties unless it is fully cross-linked, and light exposure or heat treatment for sufficient cross-linking increases manufacturing time and decreases productivity.
  • An object of the present invention is to provide a composition for forming a spacer having a significantly low viscosity and that is easily inkjet-sprayable by adding a cross-linking agent in an emulsion, which is obtained by dispersing a polymer with a relatively high weight average molecular weight with an emulsifier, so that cross-linking by light exposure or heat treatment can be done in a short time.
  • Another object of the present invention is to provide a spacer formed by using the composition.
  • Still another object of the present invention is to provide a display device comprising the spacer.
  • composition for spacer formation comprising:
  • the present invention also provides a spacer formed by the composition.
  • the present invention provides a display device comprising the spacer formed by the composition on at least one of the two opposing substrates.
  • composition for spacer formation having a viscosity of 3 to 50 cp, comprising:
  • FIG. 1 is a schematic diagram of the spacer formation process of the present invention.
  • FIG. 2 is a schematic diagram of the liquid crystal display comprising the spacer of the present invention.
  • the present invention relates to a composition for precisely forming a spacer on one of the two opposing substrates of a display device, by the inkjet method.
  • Polymer chains of the polymer emulsion used in the present invention are surrounded by an emulsifying agent, not by water, and therefore the polymer emulsion has an almost spherical microstructure. Therefore, there is little entanglement between the polymer chains, differently from the system wherein the polymer chains are disentangled lengthily in a solvent.
  • a composition using the polymer emulsion has a much lower viscosity than a polymer solution having a comparable concentration and a weight average molecular weight, and therefore spraying by inkjet is much easier.
  • a variety of polymers may be used to prepare the composition.
  • a polymer with a large weight average molecular weight can be used without significantly increasing the viscosity of the composition, it is possible to prepare the composition having good processability and capacity.
  • composition of the present invention comprises a) a polymer emulsion, b) a wetting agent, and c) a solvent.
  • the polymer emulsion of the present invention is the basic material for forming the spacer. It has sufficient hardness and elasticity, superior heat resistance and chemical resistance, and sufficient adhesivity to the substrate surface. Also, it has a sufficiently low viscosity, preferably a viscosity of 3 to 50 cp, so that it can be sprayed by inkjet when prepared as an ink.
  • the polymer emulsion is selected from a group consisting of an acryl emulsion, a urethane acryl emulsion, an epoxy acryl emulsion, a polyester acryl emulsion, and any mixture thereof.
  • the polymer emulsion has a weight average molecular weight of 300 to 50,000 and the weight average molecular weight is measured by GPC.
  • the polymer emulsion is used at from 10 to 70 parts by weight (dry weight). If the dry solid content of the polymer emulsion is below 10 parts by weight, the final height of the spacer becomes low. Otherwise, if it exceeds 70 parts by weight, it is difficult to obtain a stable emulsion.
  • the wetting agent of the present invention may be selected from a group consisting of: glycols, such as ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, and polyethylene glycol; glycerine; ethers of polyhydric alcohols, such as diethylene glycol monobutyl ether; acetates; thioglycol; and amino acids, such as glycine, methyl glycine, lucine, proline, alanine, and phenyl alanine.
  • glycols such as ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, and polyethylene glycol
  • glycerine ethers of polyhydric alcohols, such as diethylene glycol monobutyl ether
  • acetates such as thioglycol
  • amino acids such as glycine, methyl glycine, lucine, proline, alanine, and phenyl alanine.
  • the wetting agent is used from 0.1 to 50 parts by weight. If the content of the wetting agent is below 0.1 part by weight, the composition may become dry around the nozzle, and thus it may not spray. Otherwise, if it exceeds 50 parts by weight, the solid content of the composition decreases, and therefore the final height of the spacer may become low.
  • the solvent is selected from a group consisting of water, acetone, methyl ethyl ketone, methyl isobutyl ketone, methylcellosolve, ethylcellosolve, tetrahydrofuran, 1,4-dioxane, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, propylene glycol methyl ether, propylene glycol dimethyl ether, propylene glycol diethyl ether, chloroform, methylene chloride, 1,2-dichloroethane, 1,1,1-trichloroethane, 1,1,2-trichloroethane, 1,1,2-trichloroethene, hexane, heptane, octane, cyclohexane, benzene, toluene, xylene, methanol, ethanol, isopropanol, propanol, butanol
  • the solvent is used from 20 to 90 parts by weight. If the content of the solvent is below 20 parts by weight, the viscosity of the composition increases, so that it is not sprayed well. Otherwise, if it exceeds 90 parts by weight, the solid content of the composition decreases, and therefore the final height of the spacer may become low.
  • composition of the present invention may further comprise d) a cross-linking initiator and a cross-linking promoter, e) a polymeric compound having unsaturated bonds, or f) other additives to control the inkjet spraying characteristics and the physical properties and form of the spacer.
  • a cross-linking initiator and a cross-linking promoter e) a polymeric compound having unsaturated bonds
  • other additives to control the inkjet spraying characteristics and the physical properties and form of the spacer.
  • the ideal properties can be obtained with only a) the polymer emulsion, d) the cross-linking initiator and the cross-linking promoter, and e) the polymeric compound having unsaturated bonds, may not be added.
  • the spacer has good physical properties, so that it is not necessary to add a cross-linking initiator and a cross-linking promoter, or a polymeric compound having unsaturated bonds. But, spraying from the inkjet nozzle may be somewhat difficult.
  • cross-linking initiator and the cross-linking promoter of the present invention are water-soluble or soluble to the emulsifying agent. Initiation of cross-linking may be caused by light, heat, an electron beam, and so forth.
  • the cross-linking initiator is selected from a group consisting of: biimidazole compounds, such as 2,2′-bis(2-chlorophenyl)-4,4′,5,5′-tetraphenyl biimidazole and 2,2′-bis(2,3-dichlorophenyl)-4,4′,5,5′-tetraphenylbiimidazole; acetophenone compounds, such as 2-hydroxy-1-[4-(2-hydroxyethoxy)phenyl]-2-methyl-1-propane, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-(4-isopropylphenyl)-2-hydroxy-2-methylpropan-1-one, 4-(2-hydroxyethoxy)-phenyl (2-hydroxy)propyl ketone, 1-hydroxycyclohexyl phenyl ketone, benzoin methyl ether, benzoin ethyl ether, benzoin isobutyl ether, benzoin buty
  • the cross-linking promoter is selected from a group consisting of 2-mercaptobenzoimidazole, 2-mercaptobenzothiazole, 2-mercaptobenzoxazole, 2,5-dimercapto-1,3,4-thiadizole, 2-mercapto-4,6-dimethylaminopyridine, pentaerythritol tetrakis(3-mercaptopropionate), pentaerythritol tris(3-mercaptopropionate), pentaerythritol tetrakis(2-mercaptoacetate), pentaerythritol tris(2-mercaptoacetate), trimethylolpropane tris(2-mercaptoacetate), trimethylolpropane tris(3-mercaptopropionate), trimethylolethane tris(2-mercaptoacetate), and trimethylolethane tris(3-mercaptopropionate).
  • the cross-linking initiator and the cross-linking promoter are used at less than 10 parts by weight.
  • the ethylene polymeric compound having unsaturated bonds of the present invention is selected from a group consisting of: compounds obtained by esterification of polyhydric alcohols with ⁇ , ⁇ -unsaturated carboxylic acids, such as ethylene glycol di(meth)acrylate, (poly)ethylene glycol di(meth)acrylate having 2 to 14 ethylene groups, trimethylolpropane di(meth)acrylate, trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, propylene glycol di(meth)acrylate having 2 to 14 propylene groups, dipentaerythritol penta(meth)acrylate, and dipentaerythritol hexa(meth)acrylate; compounds obtained by adding (meth)acrylic acid to glycidyl-containing compounds, such as a trimethylolpropan
  • the polymeric compound having unsaturated bonds is used at less than 40 parts by weight.
  • the other additives are selected from a group consisting of: silicon-based antifoaming agents; surface tension controlling agents for cationic, anionic, zwitterionic, and non-ionic surfactants; UV absorbers, such as benzotriazole or benzophenone; light stabilizers, such as phenols or amines; anti-biocontaminants such as chloromethylphenols; chelating agents such as EDTA; oxygen absorbents such as sulfites; and thermal polymerization inhibitors, such as p-anisole, hydroquinone, pyrocatechol, t-butylcatechol, and phenothiazine.
  • the additives are used at less than 5 parts by weight.
  • any compounds that are comprised in conventional inkjet compositions may be used for the additives of d) to f) for said purposes.
  • composition of the present invention is sprayed onto a determined position of the substrate from an inkjet head.
  • the sprayed composition forms a droplet on the substrate.
  • the substrate is heated or left alone at room temperature to evaporate the solvent from the composition.
  • the spacer is formed by and cross-linking reaction using light, heat, electron beams, etc., if required.
  • the present invention can precisely form a spacer at an ideal position on at least one of the two opposing substrates of a display device, such as a liquid crystal display and an electrochromic device, by the inkjet method.
  • FIG. 1 is a schematic diagram of the spacer formation process of the present invention.
  • FIG. 2 is a schematic diagram of the liquid crystal display comprising the spacer according to one embodiment of the present invention.
  • the vertical dotted lines show that the spacer formed by the inkjet is positioned at a black matrix formation part of a color filter substrate.
  • Neocryl (Zeneca)(the polymer emulsion having a weight average molecular weight of 34,500); 20 parts by weight of glycerol, 15 parts by weight of water, and 2 parts by weight of CX100 (Zeneca) as a cross-linking emulsion were mixed well to prepare an acryl emulsion, and then filtered with a 2.5- ⁇ m filter. The viscosity was 11 cp.
  • the emulsion was sprayed through an inkjet nozzle on a glass substrate on which a transparent electrode or an alignment film was formed. Then, the substrate was dried at 80° C. for 2 minutes to evaporate the solvent, and thermal cross-linking was carried out at 150° C. for 30 minutes. As a result, a spacer with of a diameter of 25 ⁇ m and a height of 4 ⁇ m was formed. The hardness of the spacer was over 4H.
  • Ebeciyl (UCB), 15 parts by weight of glycerol, and 15 parts by weight of water were mixed to prepare an acryl emulsion, and then filtered with a 2.5- ⁇ m filter. The viscosity was 15 cp.
  • a spacer was formed as in Example 1, while omitting the thermal cross-linking step. As a result, a spacer with a diameter of 27 ⁇ m and a height of 4.5 ⁇ m was formed. The hardness of the spacer was over 2H.
  • composition comprising the polymer emulsions of Examples 1 and 2 had a much lower viscosity than the polymer solution of Comparative Example, spraying by inkjet was easy. Additionally, the spacer formed with the composition comprising the polymer emulsion with a large weight average molecular weight had better mechanical hardness than the spacer formed by the composition comprising the polymer solution. Also, as in Example 2, some spacers showed good hardness without a cross-linking step.
  • the composition for spacer formation of the present invention has a significantly low viscosity and can be easily sprayed by inkjet, so that it is useful for spacer formation in a display device such as a liquid crystal display, and an electrochromic device.

Abstract

The present invention relates to an composition for spacer formation and a spacer element using the same, and more particularly to an composition for spacer formation comprising a) 10 to 70 parts by weight (dry weight) of a polymer emulsion; b) 0.1 to 50 parts by weight of a wetting agent; and c) 20 to 90 parts by weight of a solvent, and a spacer element using the same. The composition of the present invention has a significantly low viscosity and can be sprayed easily by inkjet, so that it is useful for spacer formation in liquid crystal displays.

Description

    BACKGROUND OF THE INVENTION
  • (a) Field of the Invention
  • The present invention relates to a composition for spacer formation used for color televisions, computer monitors, and other display devices, and a spacer element using the same.
  • (b) Description of the Related Art
  • Demand for color liquid crystal displays has been on the increase in recent years, and large liquid crystal displays are being manufactured. However, manufacturing costs should be reduced in order for the color display devices to be used more widely.
  • Conventionally, a liquid crystal display is manufactured by forming a liquid crystal driving device, such as a TFT (thin film transistor), and a coloring device, such as a color filter, on a pair of opposing transparent insulating substrates. Between the substrates there are spacers that maintains a 3 to 10 μm space therebetween. Liquid crystal is injected in this space, and then the spacing is sealed to form a liquid crystal device.
  • Conventionally, spherical or cylindrical silica, alumina, or synthetic resin particles randomly distributed between the TFT substrate and the color filter substrate have been used as the spacer. But, in this case, the spacer around the light passage of the liquid crystal display may hinder driving of the liquid crystal or deteriorate the display quality due to the optical properties of the spacer itself.
  • In order to solve this problem, a method of selectively forming a spacer in the black matrix formation part through which no light passes, using a photoresist substance, has been proposed. In this case, the black matrix blocks the display quality-deteriorated part, and thus deterioration of display quality can be avoided.
  • However, when using a photoresist, the spacer formation process requires many steps including spin coating, pre-baking, exposure, developing, and post-baking of the spacer substance, and therefore the manufacturing cost increases.
  • To solve this problem, Korea Patent Publication No. 2001-0049941, Japan Patent Publication No. 2001-109002, and Japan Patent Publication No. 2001-83525 proposed a method for selectively forming a spacer on the black matrix through which no light passes, by the inkjet process.
  • Korea Patent Publication No. 2001-0049941 and Japan Patent Publication No. 2001-83525 proposed a cross-linking spacer-forming substance, which could be sprayed by the inkjet head, and which used a homopolymer or copolymer as a cross-linkable substance. Usage of the substance was limited from 0.01 to 30 parts by weight. During spacer formation, the sprayed solvent is evaporated in the cross-linking step, and only the homopolymer or copolymer forms the spacer. While the diameter of the ink droplet on the substrate surface remains almost the same due to its adhesivity, its height decreases, so that the height of the final spacer becomes significantly lower than that of the ink droplet. Accordingly, the height becomes insufficient for a high-resolution black matrix, which requires a small diameter.
  • In addition, Japan Patent Publication No. 2001-109002 proposed that it is preferable to use a monomer or oligomer with a low molecular weight, considering the spraying characteristics of the ink, while limiting the content of the solvent under 50 parts by weight and increasing the content of the spacer-forming substance. However, a substance with a low molecular weight does not have sufficient mechanical properties unless it is fully cross-linked, and light exposure or heat treatment for sufficient cross-linking increases manufacturing time and decreases productivity.
  • SUMMARY OF THE INVENTION
  • An object of the present invention is to provide a composition for forming a spacer having a significantly low viscosity and that is easily inkjet-sprayable by adding a cross-linking agent in an emulsion, which is obtained by dispersing a polymer with a relatively high weight average molecular weight with an emulsifier, so that cross-linking by light exposure or heat treatment can be done in a short time.
  • Another object of the present invention is to provide a spacer formed by using the composition.
  • Still another object of the present invention is to provide a display device comprising the spacer.
  • To attain these objects, the present invention provides a composition for spacer formation, comprising:
      • a) 10 to 70 parts by weight (dry weight) of a polymer emulsion;
      • b) 0.1 to 50 parts by weight of a wetting agent; and
      • c) 20 to 90 parts by weight of a solvent.
  • The present invention also provides a spacer formed by the composition.
  • In addition, the present invention provides a display device comprising the spacer formed by the composition on at least one of the two opposing substrates.
  • Furthermore, the present invention provides a method for preparing composition for spacer formation having a viscosity of 3 to 50 cp, comprising:
      • a) 10 to 70 parts by weight (dry weight) of a polymer emulsion;
      • b) 0.1 to 50 parts by weight of a wetting agent; and
      • c) 20 to 90 parts by weight of a solvent,
      • wherein the polymer emulsion has a weight average molecular weight of 300 to 50,000,
      • wherein the composition is applied by the inkjet method to form a spacer on one of the two opposing substrates of a display device.
    BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a schematic diagram of the spacer formation process of the present invention.
  • FIG. 2 is a schematic diagram of the liquid crystal display comprising the spacer of the present invention.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • Hereinafter, the present invention is described in more detail.
  • The present invention relates to a composition for precisely forming a spacer on one of the two opposing substrates of a display device, by the inkjet method.
  • Polymer chains of the polymer emulsion used in the present invention are surrounded by an emulsifying agent, not by water, and therefore the polymer emulsion has an almost spherical microstructure. Therefore, there is little entanglement between the polymer chains, differently from the system wherein the polymer chains are disentangled lengthily in a solvent.
  • Accordingly, a composition using the polymer emulsion has a much lower viscosity than a polymer solution having a comparable concentration and a weight average molecular weight, and therefore spraying by inkjet is much easier. Also, because even a hardly-soluble polymer can be emulsified using an appropriate emulsifying agent, a variety of polymers may be used to prepare the composition. Also, because a polymer with a large weight average molecular weight can be used without significantly increasing the viscosity of the composition, it is possible to prepare the composition having good processability and capacity.
  • The composition of the present invention comprises a) a polymer emulsion, b) a wetting agent, and c) a solvent.
  • a) The polymer emulsion of the present invention is the basic material for forming the spacer. It has sufficient hardness and elasticity, superior heat resistance and chemical resistance, and sufficient adhesivity to the substrate surface. Also, it has a sufficiently low viscosity, preferably a viscosity of 3 to 50 cp, so that it can be sprayed by inkjet when prepared as an ink.
  • Preferably, the polymer emulsion is selected from a group consisting of an acryl emulsion, a urethane acryl emulsion, an epoxy acryl emulsion, a polyester acryl emulsion, and any mixture thereof. However, it is not limited to said polymer emulsions. Preferably, the polymer emulsion has a weight average molecular weight of 300 to 50,000 and the weight average molecular weight is measured by GPC.
  • Preferably, the polymer emulsion is used at from 10 to 70 parts by weight (dry weight). If the dry solid content of the polymer emulsion is below 10 parts by weight, the final height of the spacer becomes low. Otherwise, if it exceeds 70 parts by weight, it is difficult to obtain a stable emulsion.
  • b) The wetting agent of the present invention may be selected from a group consisting of: glycols, such as ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, and polyethylene glycol; glycerine; ethers of polyhydric alcohols, such as diethylene glycol monobutyl ether; acetates; thioglycol; and amino acids, such as glycine, methyl glycine, lucine, proline, alanine, and phenyl alanine.
  • Preferably, b) the wetting agent is used from 0.1 to 50 parts by weight. If the content of the wetting agent is below 0.1 part by weight, the composition may become dry around the nozzle, and thus it may not spray. Otherwise, if it exceeds 50 parts by weight, the solid content of the composition decreases, and therefore the final height of the spacer may become low.
  • Preferably, c) the solvent is selected from a group consisting of water, acetone, methyl ethyl ketone, methyl isobutyl ketone, methylcellosolve, ethylcellosolve, tetrahydrofuran, 1,4-dioxane, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, propylene glycol methyl ether, propylene glycol dimethyl ether, propylene glycol diethyl ether, chloroform, methylene chloride, 1,2-dichloroethane, 1,1,1-trichloroethane, 1,1,2-trichloroethane, 1,1,2-trichloroethene, hexane, heptane, octane, cyclohexane, benzene, toluene, xylene, methanol, ethanol, isopropanol, propanol, butanol, t-butanol, cyclohexanone, propylene glycol methyl ether acetate, propylene glycol ethyl ether acetate, 3-methoxybutyl acetate, ethyl 3-ethoxy propionate, ethylcellosolve acetate, methylcellosolve acetate, butyl acetate, methyl ethyl ketone, methyl isobutyl ketone, ethylene glycol monomethyl ether, γ-butyl lactone, N-methylpyrrolidone, dimethylformamide, tetramethylsulfone, ethylene glycol acetate, ethyl ether acetate, ethyl lactate, polyethylene glycol, and cyclohexanone.
  • Preferably, the solvent is used from 20 to 90 parts by weight. If the content of the solvent is below 20 parts by weight, the viscosity of the composition increases, so that it is not sprayed well. Otherwise, if it exceeds 90 parts by weight, the solid content of the composition decreases, and therefore the final height of the spacer may become low.
  • The composition of the present invention may further comprise d) a cross-linking initiator and a cross-linking promoter, e) a polymeric compound having unsaturated bonds, or f) other additives to control the inkjet spraying characteristics and the physical properties and form of the spacer. In the case the ideal properties can be obtained with only a) the polymer emulsion, d) the cross-linking initiator and the cross-linking promoter, and e) the polymeric compound having unsaturated bonds, may not be added. That is, if the polymer emulsion has a large weight average molecular weight, the spacer has good physical properties, so that it is not necessary to add a cross-linking initiator and a cross-linking promoter, or a polymeric compound having unsaturated bonds. But, spraying from the inkjet nozzle may be somewhat difficult.
  • d) The cross-linking initiator and the cross-linking promoter of the present invention are water-soluble or soluble to the emulsifying agent. Initiation of cross-linking may be caused by light, heat, an electron beam, and so forth.
  • Preferably, the cross-linking initiator is selected from a group consisting of: biimidazole compounds, such as 2,2′-bis(2-chlorophenyl)-4,4′,5,5′-tetraphenyl biimidazole and 2,2′-bis(2,3-dichlorophenyl)-4,4′,5,5′-tetraphenylbiimidazole; acetophenone compounds, such as 2-hydroxy-1-[4-(2-hydroxyethoxy)phenyl]-2-methyl-1-propane, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-(4-isopropylphenyl)-2-hydroxy-2-methylpropan-1-one, 4-(2-hydroxyethoxy)-phenyl (2-hydroxy)propyl ketone, 1-hydroxycyclohexyl phenyl ketone, benzoin methyl ether, benzoin ethyl ether, benzoin isobutyl ether, benzoin butyl ether, 2,2-dimethoxy-2-phenyl acetophenone, 2-methyl-(4-methylthiophenyl)-2-morpholino-1-propan-1-one, and 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butan-1-one; benzophenone compounds, such as benzophenone, 4,4′-bis(dimethylamino)benzophenone, 4,4′-bis(diethylamino)benzophenone, 2,4,6-trimethylaminobenzophenone, methyl-o-benzoyl benzoate, 3,3-dimethyl-4-methoxybenzophenone, and 3,3′,4,4′-tetra(t-butylperoxycarbonyl)benzophenone; fluorenone compounds, such as 9-fluorenone, 2-chloro-9-fluorenone, and 2-methyl-9-fluorenone; thioxantone compounds, such as thioxantone, 2,4-diethyl thioxantone, 2-chloro thioxantone, 1-chloro-4-propyloxy thioxantone, isopropyl thioxantone, and diisopropyl thioxantone; xanthone compounds, such as xanthone and 2-methylxanthone; anthraquinone compounds, such as anthraquinone, 2-methyl anthraquinone, 2-ethyl anthraquinone, t-butyl anthraquinone, and 2,6-dichloro-9,10-anthraquinone; acridine compounds, such as 9-phenylacridine, 1,7-bis(9-acridinyl)heptane, 1,5-bis(9-acridinyl)pentane, and 1,3-bis(9-acridinyl)propane; dicarbonyl compounds, such as benzyl-1,7,7-trimethyl-bischloro[2,2,1]heptane-2,3-dione and 9,10-phenanthrenquinone; phosphine oxides, such as 2,4,6-trimethylbenzoyl diphenylphosphine oxide, bis(2,6-dimethoxybenzoyl)-2,4,4-trimethylpentyl phosphine oxide, and bis(2,6-dichlorobenzoyl)propyl phosphine oxide; methyl 4-(dimethylamino)benzoate; ethyl-4-(dimethylamino)benzoate; amine synergists, such as 2-n-butoxyethyl 4-(dimethylamino)benzoate, 2,5-bis(4-diethylaminobenzal)cyclopentanone, 2,6-bis(4-diethylaminobenzal)cyclohexanone, and 2,6-bis(4-diethylaminobenzal)-4-methyl-cyclohexanone; coumarin compounds, such as 3,3′-carbonylvinyl-7-(diethylamino)coumarin, 3-(2-benzothiazolyl)-7-(diethylamino)coumarin, 3-benzoyl-7-(diethylamino)coumarin, 3-benzoyl-7-methoxy-coumarin, and 10,10′-carbonylbis[1,1,7,7-tetramethyl-2,3,6,7-tetrahydro-1H,5H,11H-Cl]-benzopyra no[6,7,8-ij]-quinolizin-11-one; calcon compounds, such as 4-diethylamino calcon and 4-azidobenzalacetophenone; 2-benzoylmethylene; 3-methyl-β-naphthothiazoline; and (4-methylphenyl)-[4-(2-methylpropyl)-phenyl]hexafluorophosphine iodide. And, preferably, the cross-linking promoter is selected from a group consisting of 2-mercaptobenzoimidazole, 2-mercaptobenzothiazole, 2-mercaptobenzoxazole, 2,5-dimercapto-1,3,4-thiadizole, 2-mercapto-4,6-dimethylaminopyridine, pentaerythritol tetrakis(3-mercaptopropionate), pentaerythritol tris(3-mercaptopropionate), pentaerythritol tetrakis(2-mercaptoacetate), pentaerythritol tris(2-mercaptoacetate), trimethylolpropane tris(2-mercaptoacetate), trimethylolpropane tris(3-mercaptopropionate), trimethylolethane tris(2-mercaptoacetate), and trimethylolethane tris(3-mercaptopropionate).
  • Preferably, the cross-linking initiator and the cross-linking promoter are used at less than 10 parts by weight.
  • Preferably, e) the ethylene polymeric compound having unsaturated bonds of the present invention is selected from a group consisting of: compounds obtained by esterification of polyhydric alcohols with α,β-unsaturated carboxylic acids, such as ethylene glycol di(meth)acrylate, (poly)ethylene glycol di(meth)acrylate having 2 to 14 ethylene groups, trimethylolpropane di(meth)acrylate, trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, propylene glycol di(meth)acrylate having 2 to 14 propylene groups, dipentaerythritol penta(meth)acrylate, and dipentaerythritol hexa(meth)acrylate; compounds obtained by adding (meth)acrylic acid to glycidyl-containing compounds, such as a trimethylolpropane triglycidyl ether acrylic acid adduct and a bisphenol A diglycidyl ether acrylic acid adduct; esters of compounds having hydroxy groups or ethylene unsaturated bonds and polycarboxylic acids or adducts with polyisocyanates, such as a phthalic acid diester of β-hydroxyethyl (meth)acylate and a toluene diisocyanate adduct of β-hydroxyethyl (meth)acrylate; and (meth)acrylic acid alkyl esters, such as methyl (meth)acrylate, ethyl (meth)acrylate, butyl (meth)acrylate, and 2-ethylhexyl (meth)acrylate.
  • Preferably, the polymeric compound having unsaturated bonds is used at less than 40 parts by weight.
  • Preferably, f) the other additives are selected from a group consisting of: silicon-based antifoaming agents; surface tension controlling agents for cationic, anionic, zwitterionic, and non-ionic surfactants; UV absorbers, such as benzotriazole or benzophenone; light stabilizers, such as phenols or amines; anti-biocontaminants such as chloromethylphenols; chelating agents such as EDTA; oxygen absorbents such as sulfites; and thermal polymerization inhibitors, such as p-anisole, hydroquinone, pyrocatechol, t-butylcatechol, and phenothiazine. Preferably, the additives are used at less than 5 parts by weight.
  • In the present invention, any compounds that are comprised in conventional inkjet compositions may be used for the additives of d) to f) for said purposes.
  • The composition of the present invention is sprayed onto a determined position of the substrate from an inkjet head. The sprayed composition forms a droplet on the substrate. Then, the substrate is heated or left alone at room temperature to evaporate the solvent from the composition. The spacer is formed by and cross-linking reaction using light, heat, electron beams, etc., if required.
  • Accordingly, the present invention can precisely form a spacer at an ideal position on at least one of the two opposing substrates of a display device, such as a liquid crystal display and an electrochromic device, by the inkjet method.
  • FIG. 1 is a schematic diagram of the spacer formation process of the present invention. FIG. 2 is a schematic diagram of the liquid crystal display comprising the spacer according to one embodiment of the present invention. In said drawings, the vertical dotted lines show that the spacer formed by the inkjet is positioned at a black matrix formation part of a color filter substrate.
  • Hereinafter, the present invention is described in more detail through Examples and a Comparative Example. However, the following Examples are only for the understanding of the present invention, and the present invention is not limited by the following Examples.
  • Example 1
  • 63 parts by weight of Neocryl (Zeneca)(the polymer emulsion having a weight average molecular weight of 34,500); 20 parts by weight of glycerol, 15 parts by weight of water, and 2 parts by weight of CX100 (Zeneca) as a cross-linking emulsion were mixed well to prepare an acryl emulsion, and then filtered with a 2.5-μm filter. The viscosity was 11 cp. The emulsion was sprayed through an inkjet nozzle on a glass substrate on which a transparent electrode or an alignment film was formed. Then, the substrate was dried at 80° C. for 2 minutes to evaporate the solvent, and thermal cross-linking was carried out at 150° C. for 30 minutes. As a result, a spacer with of a diameter of 25 μm and a height of 4 μm was formed. The hardness of the spacer was over 4H.
  • Example 2
  • 70 parts by weight of Ebeciyl (UCB), 15 parts by weight of glycerol, and 15 parts by weight of water were mixed to prepare an acryl emulsion, and then filtered with a 2.5-μm filter. The viscosity was 15 cp. A spacer was formed as in Example 1, while omitting the thermal cross-linking step. As a result, a spacer with a diameter of 27 μm and a height of 4.5 μm was formed. The hardness of the spacer was over 2H.
  • Comparative Example
  • 47 parts by weight of polyethylene glycol diacrylate (having a weight average molecular weight of 8,900) as water-soluble monomer, 20 parts by weight of ethoxytrimethylolpropane triacrylate ester, 10 parts by weight of glycerol, 20 parts by weight of water, and 3 parts by weight of Irgacure 2959 (Ciba Specialty Chemicals) as a photo initiator were mixed to prepare a composition by the conventional method, and then filtered with a 2.5-μm filter. The viscosity was 27 cp. The composition was sprayed through an inkjet nozzle on a glass substrate. After 3 minutes of pre-baking at 70° C., UV was irradiated for 3 minutes and post-baking was carried out at 150° C. for 30 minutes. As a result, a spacer with a diameter of 50 μm and a height of 3 μm and a satellite of a meter of 10 μm and a height of 1 μm were formed. The hardness of the spacer was about HB.
  • Because the composition comprising the polymer emulsions of Examples 1 and 2 had a much lower viscosity than the polymer solution of Comparative Example, spraying by inkjet was easy. Additionally, the spacer formed with the composition comprising the polymer emulsion with a large weight average molecular weight had better mechanical hardness than the spacer formed by the composition comprising the polymer solution. Also, as in Example 2, some spacers showed good hardness without a cross-linking step.
  • As described above, the composition for spacer formation of the present invention has a significantly low viscosity and can be easily sprayed by inkjet, so that it is useful for spacer formation in a display device such as a liquid crystal display, and an electrochromic device.
  • While the present invention has been described in detail with reference to the preferred embodiments, those skilled in the art will appreciate that various modifications and substitutions can be made thereto without departing from the spirit and scope of the present invention as set forth in the appended claims.

Claims (16)

1. An composition for spacer formation having a viscosity of 3 to 50 cp, comprising:
a) 10 to 70 parts by weight (dry weight) of a polymer emulsion;
b) 0.1 to 50 parts by weight of a wetting agent; and
c) 20 to 90 parts by weight of a solvent,
wherein the polymer emulsion has a weight average molecular weight of 300 to 50,000,
wherein the composition is applied in a spacer formation of a display device.
2. The composition for spacer formation according to claim 1, wherein a) the polymer emulsion is selected from a group consisting of an acryl emulsion, a urethane acryl emulsion, an epoxy acryl emulsion, a polyester acryl emulsion, and any mixture thereof.
3. The composition according to claim 1, wherein b) the wetting agent is selected from a group consisting of glycols, glycerine, ethers of polyhydric alcohols, acetates of polyhydric alcohols, thioglycol, and amino acids.
4. The composition according to claim 1, wherein c) the solvent is selected from a group consisting of water, acetone, methyl ethyl ketone, methyl isobutyl ketone, methylcellosolve, ethylcellosolve, tetrahydrofuran, 1,4-dioxane, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, propylene glycol methyl ether, propylene glycol dimethyl ether, propylene glycol diethyl ether, chloroform, methylene chloride, 1,2-dichloroethane, 1,1,1-trichloroethane, 1,1,2-trichloroethane, 1,1,2-trichloroethene, hexane, heptane, octane, cyclohexane, benzene, toluene, xylene, methanol, ethanol, isopropanol, propanol, butanol, t-butanol, cyclohexanone, propylene glycol methyl ether acetate, propylene glycol ethyl ether acetate, 3-methoxybutyl acetate, ethyl 3-ethoxy propionate, ethylcellosolve acetate, methylcellosolve acetate, butyl acetate, methyl ethyl ketone, methyl isobutyl ketone, ethylene glycol monomethyl ether, γ-butyl lactone, N-methylpyrrolidone, dimethylformamide, tetramethylsulfone, ethylene glycol acetate, ethyl ether acetate, ethyl lactate, polyethylene glycol, and cyclohexanone.
5. The composition according to claim 1, which further comprises d) less than 10 parts by weight of a cross-linking initiator and a cross-linking promoter; or e) less than 40 parts by weight of a polymeric compound having unsaturated bonds.
6. The composition according to claim 1, which further comprises f) less than 5 parts by weight of additives selected from a group consisting of an antifoaming agent, a surface tension controlling agent, a light stabilizer, an anti-biocontaminant, an oxygen absorbent, and a thermal polymerization inhibitor.
7. A spacer formed by the composition according to claim 1.
8. A display device comprising the spacer according to claim 7 on at least one of the two opposing substrates.
9. A display device according to claim 8, wherein the display device is a liquid crystal display or an electrochromic device.
10. A method for preparing composition for spacer formation having a viscosity of 3 to 50 cp, comprising:
a) 10 to 70 parts by weight (dry weight) of a polymer emulsion;
b) 0.1 to 50 parts by weight of a wetting agent; and
c) 20 to 90 parts by weight of a solvent,
wherein the polymer emulsion has a weight average molecular weight of 300 to 50,000,
wherein the composition is applied by the inkjet method to form a spacer on one of the two opposing substrates of a display device.
11. The method according to claim 10, wherein the display device is a liquid crystal display or an electrochromic device.
12. The method according to claim 10, wherein a) the polymer emulsion is selected from a group consisting of an acryl emulsion, a urethane acryl emulsion, an epoxy acryl emulsion, a polyester acryl emulsion, and any mixture thereof.
13. The method according to claim 10, wherein b) the wetting agent is selected from a group consisting of glycols, glycerine, ethers of polyhydric alcohols, acetates of polyhydric alcohols, thioglycol, and amino acids.
14. The method according to claim 10, wherein c) the solvent is selected from a group consisting of water, acetone, methyl ethyl ketone, methyl isobutyl ketone, methylcellosolve, ethylcellosolve, tetrahydrofuran, 1,4-dioxane, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, propylene glycol methyl ether, propylene glycol dimethyl ether, propylene glycol diethyl ether, chloroform, methylene chloride, 1,2-dichloroethane, 1,1,1-trichloroethane, 1,1,2-trichloroethane, 1,1,2-trichloroethene, hexane, heptane, octane, cyclohexane, benzene, toluene, xylene, methanol, ethanol, isopropanol, propanol, butanol, t-butanol, cyclohexanone, propylene glycol methyl ether acetate, propylene glycol ethyl ether acetate, 3-methoxybutyl acetate, ethyl 3-ethoxy propionate, ethylcellosolve acetate, methylcellosolve acetate, butyl acetate, methyl ethyl ketone, methyl isobutyl ketone, ethylene glycol monomethyl ether, γ-butyl lactone, N-methylpyrrolidone, dimethylformamide, tetramethylsulfone, ethylene glycol acetate, ethyl ether acetate, ethyl lactate, polyethylene glycol, and cyclohexanone.
15. The method according to claim 10, which further comprises d) less than 10 parts by weight of a cross-linking initiator and a cross-linking promoter; or e) less than 40 parts by weight of a polymeric compound having unsaturated bonds.
16. The method according to claim 10, which further comprises f) less than 5 parts by weight of additives selected from a group consisting of an antifoaming agent, a surface tension controlling agent, a light stabilizer, an anti-biocontaminant, an oxygen absorbent, and a thermal polymerization inhibitor.
US11/671,300 2003-01-22 2007-02-05 Composition for inkjet spacer formation and spacer element using the same Abandoned US20070190429A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/671,300 US20070190429A1 (en) 2003-01-22 2007-02-05 Composition for inkjet spacer formation and spacer element using the same

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
KR10-2003-0004269A KR100508908B1 (en) 2003-01-22 2003-01-22 Ink composition for inkjet spacer-form and spacer element using thereof
KR10-2003-0004269 2003-01-22
US10/496,893 US7328988B2 (en) 2003-01-22 2003-08-13 Ink composition for inkjet spacer formation and spacer element using the same
US11/671,300 US20070190429A1 (en) 2003-01-22 2007-02-05 Composition for inkjet spacer formation and spacer element using the same

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US10/496,893 Continuation-In-Part US7328988B2 (en) 2003-01-22 2003-08-13 Ink composition for inkjet spacer formation and spacer element using the same

Publications (1)

Publication Number Publication Date
US20070190429A1 true US20070190429A1 (en) 2007-08-16

Family

ID=32768544

Family Applications (2)

Application Number Title Priority Date Filing Date
US10/496,893 Expired - Lifetime US7328988B2 (en) 2003-01-22 2003-08-13 Ink composition for inkjet spacer formation and spacer element using the same
US11/671,300 Abandoned US20070190429A1 (en) 2003-01-22 2007-02-05 Composition for inkjet spacer formation and spacer element using the same

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US10/496,893 Expired - Lifetime US7328988B2 (en) 2003-01-22 2003-08-13 Ink composition for inkjet spacer formation and spacer element using the same

Country Status (5)

Country Link
US (2) US7328988B2 (en)
JP (1) JP2006504857A (en)
KR (1) KR100508908B1 (en)
AU (1) AU2003251199A1 (en)
WO (1) WO2004065502A1 (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006243502A (en) * 2005-03-04 2006-09-14 Sharp Corp Forming method for spacer for liquid crystal display element, and liquid crystal display element with spacer formed by the method
WO2006095556A1 (en) * 2005-03-11 2006-09-14 Hitachi Maxell, Ltd. Oil based pigment ink composition
JP2006249388A (en) * 2005-03-14 2006-09-21 Fuji Photo Film Co Ltd Ink composition, method for forming image using the same and recorded product
KR100729557B1 (en) * 2005-05-24 2007-06-18 연세대학교 산학협력단 Photonic crystal ink composition for inkjet printing, method for forming 3-dimensional photonic crystal by inkjet printing and 3-dimensional photonic crystal device manufactured by the method
GB0519941D0 (en) * 2005-09-30 2005-11-09 Xennia Technology Ltd Inkjet printing
US8840231B2 (en) * 2005-10-04 2014-09-23 Hewlett-Packard Development Company, L.P. Ink-jet printing methods compositions providing improved image durability
WO2007114145A1 (en) 2006-04-06 2007-10-11 Hitachi Chemical Company, Ltd. Ink for forming liquid crystal spacer and liquid crystal display device using such ink
US7803420B2 (en) * 2006-12-01 2010-09-28 Applied Materials, Inc. Methods and apparatus for inkjetting spacers in a flat panel display
CN101802694B (en) * 2007-09-05 2012-07-11 日立化成工业株式会社 Process for producing spacer for liquid crystal display apparatus, ink for spacer formation, liquid crystal display apparatus and process for manufacturing the same
JP5282293B2 (en) * 2007-11-14 2013-09-04 コニカミノルタ株式会社 Ink-jet ink for non-water-absorbing recording medium and ink-jet recording method
KR101475312B1 (en) * 2007-11-28 2014-12-22 엘지디스플레이 주식회사 Composition of column spacer and method of fabricating liquid crystal display device using the same
US9169409B2 (en) * 2008-11-07 2015-10-27 Lg Display Co., Ltd. Ink composition for imprint lithography and roll printing
KR101210987B1 (en) * 2009-10-26 2012-12-11 주식회사 엘지화학 Inkjet composition for forming transparent film and preparation methode thereof
CN105062503B (en) * 2015-07-24 2017-07-07 北京中融安全印务公司 It is a kind of to can be used for liquid crystal material of ink-jet and preparation method thereof
CN110383168B (en) 2017-02-01 2023-04-28 分子印记公司 Configuring optical layers in imprint lithography processes
CN110903698A (en) * 2019-12-06 2020-03-24 广州亦盛环保科技有限公司 Water-based thermosetting ink and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020150698A1 (en) * 2001-04-13 2002-10-17 Fuji Photo Film Co., Ltd. Liquid crystal composition, color filter and liquid crystal display device
US20030036018A1 (en) * 2001-07-31 2003-02-20 Chun-Hsien Li Radiation-sensitive resin composition for spacer
US20040069364A1 (en) * 2002-07-10 2004-04-15 Seiko Epson Corporation Method of disposing spacer and method of manufacturing electro-optic device
US20070008603A1 (en) * 2005-07-11 2007-01-11 Sotzing Gregory A Electrochromic devices utilizing very low band gap conjugated counter electrodes: preparation and use
US20070059901A1 (en) * 2005-09-15 2007-03-15 Eastman Kodak Company Metal and electronically conductive polymer transfer

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59221923A (en) * 1983-05-31 1984-12-13 日本黒鉛工業株式会社 Method of producing flexible thin keyboard switch member
JP2572585B2 (en) * 1987-01-29 1997-01-16 ぺんてる株式会社 Aqueous printing ink composition
US5216096A (en) * 1991-09-24 1993-06-01 Japan Synthetic Rubber Co., Ltd. Process for the preparation of cross-linked polymer particles
US5494769A (en) * 1993-01-11 1996-02-27 Nippon Paint Co., Ltd. Polyurea-covered particle having narrow particle size distribution and its production
DE19805121A1 (en) * 1998-02-09 1999-08-12 Basf Ag Process for the preparation of dye-containing, aqueous polymer dispersions
JP2001042338A (en) 1999-07-29 2001-02-16 Canon Inc Liquid crystal element and its manufacture and substrate having spacer
JP4379974B2 (en) 1999-10-18 2009-12-09 キヤノン株式会社 Manufacturing method of liquid crystal element
JP2001109002A (en) 1999-10-07 2001-04-20 Canon Inc Color filter with spacer, its production and liquid crystal device using that color filter
JP2001083525A (en) 1999-09-09 2001-03-30 Canon Inc Color filter with spacer, its production and liquid crystal device using that color filter
JP3846141B2 (en) * 2000-01-18 2006-11-15 富士ゼロックス株式会社 Method for producing polymer particles
EP1262529A1 (en) * 2001-05-29 2002-12-04 Ricoh Company, Ltd. Ink set for ink jet recording, method for ink jet recording
AU785239B2 (en) * 2001-06-20 2006-11-23 Rohm And Haas Company Aqueous composite particle composition
JP3787505B2 (en) 2001-06-28 2006-06-21 株式会社日立製作所 Information recording device

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020150698A1 (en) * 2001-04-13 2002-10-17 Fuji Photo Film Co., Ltd. Liquid crystal composition, color filter and liquid crystal display device
US20030036018A1 (en) * 2001-07-31 2003-02-20 Chun-Hsien Li Radiation-sensitive resin composition for spacer
US20040069364A1 (en) * 2002-07-10 2004-04-15 Seiko Epson Corporation Method of disposing spacer and method of manufacturing electro-optic device
US20070008603A1 (en) * 2005-07-11 2007-01-11 Sotzing Gregory A Electrochromic devices utilizing very low band gap conjugated counter electrodes: preparation and use
US20070059901A1 (en) * 2005-09-15 2007-03-15 Eastman Kodak Company Metal and electronically conductive polymer transfer

Also Published As

Publication number Publication date
KR20040067247A (en) 2004-07-30
AU2003251199A1 (en) 2004-08-13
US7328988B2 (en) 2008-02-12
KR100508908B1 (en) 2005-08-17
US20040257416A1 (en) 2004-12-23
WO2004065502A1 (en) 2004-08-05
JP2006504857A (en) 2006-02-09

Similar Documents

Publication Publication Date Title
US20070190429A1 (en) Composition for inkjet spacer formation and spacer element using the same
CN102103327B (en) Black matrix composition with high light-shielding and improved adhesion properties
KR101899290B1 (en) Colored photosensitive resin composition, color filter and display device
JP5154915B2 (en) Alkali-soluble resin having main chain ring structure and use thereof
CN101622577A (en) Radiation sensitive resin composition, spacer for liquid crystal display element and diaphragm and their formation method
WO2013031736A1 (en) Negative photosensitive resin composition, partition wall, black matrix and optical element
US9034561B2 (en) Photosensitive composition comprising an acrylate compound
CN101666975A (en) Coloring radiation sensitive composition, color filter and color liquid crystal display elements
KR20150119067A (en) Blocked isocyanato group-containing polymer, composition containing polymer, and applications thereof
KR101430806B1 (en) Fluorine-based resins and photosensitive resin composition comprising the same
KR20110073372A (en) Photosensitive resin composition which has advanced pattern adhesion and developing property
KR101498776B1 (en) New compound, photosensitive composition comprising the same and photosensitive material
JP2007277512A (en) Light- and heat-curable resin composition for column spacer, column spacer and liquid crystal display element
JP2007231205A (en) Curable resin composition for column spacer, column spacer and liquid crystal-displaying element
JP2009149804A (en) Side chain double bond-containing modified polymer for slit coating, and use of the same
US20120178863A1 (en) Inkjet composition for forming a transparent film, and transparent film formed from same
JP2018002962A (en) Photopolymerizable composition, cured product, image display device and oxime ester compound
JP5033430B2 (en) Projection forming composition for liquid crystal alignment control
US8742005B2 (en) Acrylate-based compounds and photosensitive composition comprising the same
JP2007063531A (en) Curable resin composition, column spacer and liquid crystal display device
JP5076511B2 (en) Projection forming composition for liquid crystal alignment control
KR101604151B1 (en) Photosensitive resin composition and photosensitive material using the same
CN103718110A (en) Photosensitive composition and compound used therein
KR101492679B1 (en) Polymer and photo-sensitive resin composition comprising the same
JP2006189584A (en) Curable resin composition for columnar spacer, the columnar spacer and liquid crystal display element

Legal Events

Date Code Title Description
AS Assignment

Owner name: LG CHEM, LTD., KOREA, REPUBLIC OF

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KIM, JOON-HYUNG;KONG, YOUNG-SUN;KIM, KYUNG-JUN;REEL/FRAME:020363/0146

Effective date: 20071218

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION