Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
  • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
  • C08F290/06—Polymers provided for in subclass C08G
  • C08F290/064—Polymers containing more than one epoxy group per molecule
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
  • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
  • C08F290/06—Polymers provided for in subclass C08G
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/14—Polycondensates modified by chemical after-treatment
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/14—Polycondensates modified by chemical after-treatment
  • C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
  • C08G59/1438—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
  • C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
  • C08G59/4014—Nitrogen containing compounds
  • C08G59/4035—Hydrazines; Hydrazides
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K3/00—Materials not provided for elsewhere
  • C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
• • G—PHYSICS
  • G02—OPTICS
  • G02F—OPTICAL 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
  • G02F1/00—Devices 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
  • G02F1/01—Devices 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 
  • G02F1/13—Devices 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
  • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
  • G02F1/1333—Constructional arrangements; Manufacturing methods
  • G02F1/1339—Gaskets; Spacers; Sealing of cells

Definitions

• the present invention relates to a sealant for display elements that is excellent in flexibility responsiveness, adhesion to alignment films, adhesion in high temperature and high humidity environments, and moisture permeation prevention properties.
• the present invention also relates to a liquid crystal display element sealant and a liquid crystal display element using the display element sealant.
• liquid crystal display elements In recent years, liquid crystal display elements, organic EL display elements, and the like have been widely used as display elements having characteristics such as thinness, light weight, and low power consumption.
• liquid crystals, light-emitting layers, etc. are usually sealed with a sealant made of a curable resin composition.
• a sealant made of a curable resin composition.
• a dripping method using a sealant as disclosed in Patent Document 1 and Patent Document 2 is used as disclosed in Patent Document 1 and Patent Document 2 is used.
• a liquid crystal dropping method called ⁇ LCD'' is used.
• ⁇ LCD'' In the drip method, first, a frame-shaped seal pattern is formed on one of two electrode-attached substrates by dispensing.
• liquid crystal display elements are increasingly required to be reliable when operating in high temperature and high humidity environments, and sealants for display elements are designed to prevent water from entering from outside.
• sealants for display elements are designed to prevent water from entering from outside.
• the adhesiveness of the display element sealant and to improve the moisture permeation prevention property of the display element sealant.
• the line width of the sealant for display elements that is applied has become thinner, and it is therefore necessary to obtain a sealant for display elements that is excellent in both adhesion and moisture permeability even when the lines are thinned. was difficult.
• the present disclosure 1 is a display element sealant containing a curable resin, and the curable resin is a display element sealant containing a compound represented by the following formula (1).
• the present disclosure 2 is the sealant for a display element according to the present disclosure 1, in which the two Y's in the following formula (1) have the same structure.
• the present disclosure 3 is the sealant for a display element according to the present disclosure 1 or 2, wherein at least one Y in the following formula (1) has a structure containing two or more aromatic rings.
• the present disclosure 4 is the sealant for a display element according to the present disclosure 3, in which at least one Y in the following formula (1) has a structure represented by the following formula (3).
• the present disclosure 5 is a sealant for a liquid crystal display element using the display element sealant of the present disclosure 1, 2, 3, or 4.
• the present disclosure 6 is a liquid crystal display element having a cured product of the liquid crystal display element sealant of the present disclosure 5.
• R 1 and R 2 each independently represent a group represented by the following formula (2-1) or (2-2), and X is a straight group having 6 to 20 carbon atoms. It represents a chain or branched hydrocarbon group, and the two Y's may be the same or different, and represent a structure containing an aromatic ring.
• R 3 represents a hydrogen atom or a methyl group.
• * represents a bonding position
• R 4 and R 5 each independently represent a hydrogen atom or a methyl group.
• the present invention will be explained in detail below.
• the present inventor has considered using a compound having a long-chain hydrocarbon group or a compound having a rubber structure as a curable resin in order to improve the flexibility response of the sealant.
• sealants obtained using such compounds sometimes have poor moisture permeability prevention properties and adhesive properties under high temperature and high humidity environments. Therefore, as a result of further intensive studies, the present inventors found that by using a compound with a specific structure as a curable resin, flexibility responsiveness, adhesion to alignment films, adhesion under high temperature and high humidity environments, and prevention of moisture permeation were achieved.
• the inventors have discovered that a sealant for display elements with excellent properties can be obtained, and have completed the present invention.
• the sealant for display elements of the present invention contains a curable resin.
• the above-mentioned curable resin contains a compound represented by the above formula (1).
• the sealant for display elements of the present invention has excellent flexibility responsiveness, adhesion to alignment films, adhesion under high temperature and high humidity environments, and moisture permeation prevention properties. It will be excellent in
• X represents a linear or branched hydrocarbon group having 6 to 20 carbon atoms.
• the hydrocarbon group represented by X above may be a saturated hydrocarbon group or an unsaturated hydrocarbon group.
• the hydrocarbon group represented by X preferably has 11 or more carbon atoms.
• the number of carbon atoms in the hydrocarbon group represented by X is preferably 19 or more.
• the number of carbon atoms in the hydrocarbon group represented by X is preferably 14 or less.
• the two Y's may be the same or different, and represent a structure containing an aromatic ring. It is preferable that the two Y's in the above formula (1) have the same structure.
• at least one Y is selected from the viewpoint of further improving the adhesiveness of the resulting display element sealant to the alignment film, the adhesiveness in a high temperature and high humidity environment, and the moisture permeation prevention property. , a structure containing two or more aromatic rings is preferable, and a structure represented by the above formula (3) is more preferable.
• the method for producing the compound in which R 1 and R 2 in the above formula (1) are groups represented by the above formula (2-1) includes, for example, Examples include the following methods. That is, first, a dicarboxylic acid having a carboxy group at both ends of a hydrocarbon group represented by X above, and a bifunctional epoxy compound having a glycidyloxy group at both ends of a structure containing an aromatic ring represented by Y above. are reacted by heating in the presence of a catalyst and a polymerization inhibitor. Next, by washing the obtained product with water, a compound in which R 1 and R 2 in the above formula (1) are groups represented by the above formula (2-1) can be obtained.
• the following methods may be mentioned. That is, first, a dicarboxylic acid having a carboxy group at both ends of a hydrocarbon group represented by X above, and a bifunctional epoxy compound having a glycidyloxy group at both ends of a structure containing an aromatic ring represented by Y above.
• (meth)acrylic acid After reacting by heating in the presence of a catalyst and a polymerization inhibitor, (meth)acrylic acid is further added, and all or part of the epoxy groups are reacted with the (meth)acrylic acid. Next, by washing the obtained product with water, a compound in which R 1 and R 2 in the above formula (1) are groups represented by the above formula (2-2), or a compound in the above formula (1) is obtained. A compound in which one of R 1 and R 2 is a group represented by the above formula (2-1) and the other is a group represented by the above formula (2-2) can be obtained.
• the above-mentioned "(meth)acrylic" means acrylic or methacryl.
• dicarboxylic acids examples include eicosadienoic acid, 8,12-icosadienedioic acid, 8,-13-dimethyl-8,12-icosadienedioic acid, hexadecanedioic acid, dodecanedioic acid, suberic acid, azelaic acid, and sebacindioic acid. acids, nonamethylene dicarboxylic acid, brassylic acid, tetradecanedioic acid, pentadecanedioic acid, heptadecanedioic acid, nonadecanedioic acid, octadecanedioic acid, and the like.
• bifunctional epoxy compounds include bisphenol A diglycidyl ether, bisphenol F diglycidyl ether, bisphenol E diglycidyl ether, resorcinol diglycidyl ether, 1,5-hexadiene diepoxide, tetramethylene glycol diglycidyl ether, 2, 2'-(2,2,3,3,4,4,5,5-octafluorohexane-1,6-diyl)bis(oxirane), 9,9-bis(4-glycidyloxyphenyl)fluorene, 9 , 9-bis(4-hydroxy-3-methylphenyl)fluorenedieglycidyl ether, neopentyl glycol diglycidyl ether, diglycidyl 1,2-cyclohexanedicarboxylate, diglycidyl 4-cyclohexene-1,2-dicarboxylate, 1,7 - Octadiene diepoxide and the like.
• those include bisphenol A digly
• the above-mentioned curable resin may contain other curable resins in addition to the compound represented by the above formula (1) for the purpose of further improving the moisture permeability prevention property.
• the preferable lower limit of the content of the compound represented by the formula (1) in 100 parts by weight of the curable resin is 10 parts by weight, and the preferable upper limit is 80 parts by weight.
• the content of the compound represented by the above formula (1) is 10 parts by weight or more, the resulting display element sealant has flexibility responsiveness, adhesion to alignment films, and adhesion under high temperature and high humidity environments. It will be better due to its properties.
• the content of the compound represented by the above formula (1) is 80 parts by weight or less, the resulting display element sealant has better moisture permeation prevention properties.
• a more preferable lower limit of the content of the compound represented by the above formula (1) is 20 parts by weight, and a more preferable upper limit is 50 parts by weight.
• Examples of the other curable resin include other epoxy compounds and other (meth)acrylic compounds other than those contained in the compound represented by formula (1) above.
• Examples of the other epoxy compounds mentioned above include bisphenol A type epoxy compounds, bisphenol F type epoxy compounds, bisphenol E type epoxy compounds, bisphenol S type epoxy compounds, 2,2'-diallylbisphenol A type epoxy compounds, and hydrogenated bisphenol type epoxy compounds.
• Epoxy compounds, propylene oxide-added bisphenol A type epoxy compounds, resorcinol type epoxy compounds, biphenyl type epoxy compounds, sulfide type epoxy compounds, diphenyl ether type epoxy compounds, dicyclopentadiene type epoxy compounds, naphthalene type epoxy compounds, phenol novolac type epoxy compounds, Orthocresol novolac type epoxy compound, dicyclopentadiene novolac type epoxy compound, biphenyl novolac type epoxy compound, naphthalenephenol novolac type epoxy compound, glycidylamine type epoxy compound, alkyl polyol type epoxy compound, rubber modified epoxy compound, glycidyl ester compound, etc. can be mentioned.
• bisphenol A-type epoxy compounds include, for example, jER828EL, jER1004 (both manufactured by Mitsubishi Chemical Corporation), and EPICLON EXA-850CRP (manufactured by DIC Corporation).
• bisphenol F-type epoxy compounds include, for example, jER806, jER4004 (both manufactured by Mitsubishi Chemical Corporation), and EPICLON EXA-830CRP (manufactured by DIC Corporation).
• commercially available ones include, for example, Epomic R710 (manufactured by Mitsui Chemicals).
• bisphenol S-type epoxy compounds include, for example, EPICLON EXA-1514 (manufactured by DIC).
• commercially available ones include, for example, RE-810NM (manufactured by Nippon Kayaku Co., Ltd.).
• commercially available ones include, for example, EPICLON EXA-7015 (manufactured by DIC Corporation).
• propylene oxide-added bisphenol A type epoxy compounds include, for example, EP-4000S (manufactured by ADEKA).
• commercially available resorcinol-type epoxy compounds include, for example, EX-201 (manufactured by Nagase ChemteX).
• biphenyl-type epoxy compounds include, for example, jER YX-4000H (manufactured by Mitsubishi Chemical Corporation).
• sulfide type epoxy compounds commercially available ones include, for example, YSLV-50TE (manufactured by Nippon Steel Chemical & Materials Co., Ltd.).
• diphenyl ether type epoxy compounds commercially available ones include, for example, YSLV-80DE (manufactured by Nippon Steel Chemical & Materials Co., Ltd.).
• dicyclopentadiene type epoxy compounds include, for example, EP-4088S (manufactured by ADEKA).
• naphthalene type epoxy compounds include, for example, EPICLON HP-4032 and EPICLON EXA-4700 (both manufactured by DIC).
• EPICLON HP-4032 and EPICLON EXA-4700 both manufactured by DIC.
• EPICLON N-770 manufactured by DIC
• EPICLON N-670-EXP-S manufactured by DIC Corporation
• dicyclopentadiene novolak type epoxy compounds commercially available ones include, for example, EPICLON HP-7200 (manufactured by DIC Corporation).
• biphenyl novolac type epoxy compounds include, for example, NC-3000P (manufactured by Nippon Kayaku Co., Ltd.).
• naphthalenephenol novolac type epoxy compounds commercially available ones include, for example, ESN-165S (manufactured by Nippon Steel Chemical & Materials Co., Ltd.).
• glycidylamine type epoxy compounds include jER630 (manufactured by Mitsubishi Chemical Corporation), EPICLON430 (manufactured by DIC Corporation), and TETRAD-X (manufactured by Mitsubishi Gas Chemical Company).
• alkyl polyol type epoxy compounds commercially available ones include, for example, ZX-1542 (manufactured by Nippon Steel Chemical & Materials Co., Ltd.), EPICLON726 (manufactured by DIC Corporation), Epolite 80MFA (manufactured by Kyoeisha Chemical Co., Ltd.), and Denacol EX- 611 (manufactured by Nagase ChemteX).
• commercially available rubber-modified epoxy compounds include, for example, YR-450, YR-207 (all manufactured by Nippon Steel Chemical & Materials), and Epolead PB (manufactured by Daicel Corporation).
• Examples of commercially available glycidyl ester compounds include Denacol EX-147 (manufactured by Nagase ChemteX).
• Other commercially available epoxy compounds mentioned above include, for example, YDC-1312, YSLV-80XY, YSLV-90CR (all manufactured by Nippon Steel Chemical & Materials), XAC4151 (manufactured by Asahi Kasei Corporation), jER1031, and jER1032. (all manufactured by Mitsubishi Chemical), EXA-7120 (manufactured by DIC), and TEPIC (manufactured by Nissan Chemical).
• partially (meth)acrylic modified epoxy compounds are also suitably used.
• the above-mentioned partially (meth)acrylic modified epoxy compound can be obtained by reacting some epoxy groups of an epoxy compound having two or more epoxy groups with (meth)acrylic acid. It means a compound having one or more epoxy groups and one or more (meth)acryloyl groups in one molecule.
• the above-mentioned "(meth)acryloyl” means acryloyl or methacryloyl.
• Examples of the other (meth)acrylic compounds include (meth)acrylic acid ester compounds, epoxy (meth)acrylates, urethane (meth)acrylates, and the like. Among them, epoxy (meth)acrylate is preferred. Further, the other (meth)acrylic compound mentioned above preferably has two or more (meth)acryloyl groups in the molecule from the viewpoint of reactivity.
• the above-mentioned "(meth)acrylate” means acrylate or methacrylate, and the above-mentioned “epoxy (meth)acrylate” refers to the reaction of all epoxy groups in an epoxy compound with (meth)acrylic acid. It refers to a compound that has been
• examples of monofunctional ones include methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, n-butyl (meth)acrylate, and isobutyl (meth)acrylate.
• t-butyl (meth)acrylate 2-ethylhexyl (meth)acrylate, n-octyl (meth)acrylate, isooctyl (meth)acrylate, isononyl (meth)acrylate, isodecyl (meth)acrylate, lauryl (meth)acrylate, iso myristyl (meth)acrylate, stearyl (meth)acrylate, 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 2-hydroxybutyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate, cyclohexyl ( meth)acrylate, isobornyl (meth)acrylate, bicyclopentenyl (meth)acrylate, benzyl (meth)acrylate, 2-methoxyethyl (meth)acrylate, 2-ethoxyethyl (meth)acrylate, 2-butoxyethyl (
• examples of difunctional ones include 1,3-butanediol di(meth)acrylate, 1,4-butanediol di(meth)acrylate, and 1,6-hexane di(meth)acrylate.
• Examples of the epoxy (meth)acrylate include those obtained by reacting an epoxy compound and (meth)acrylic acid in the presence of a basic catalyst according to a conventional method.
• epoxy compound serving as a raw material for synthesizing the epoxy (meth)acrylate the same epoxy compounds as the other epoxy compounds mentioned above can be used.
• epoxy (meth)acrylates commercially available ones include epoxy (meth)acrylate manufactured by Daicel Allnex, epoxy (meth)acrylate manufactured by Shin-Nakamura Chemical Co., Ltd., and epoxy (meth)acrylate manufactured by Kyoeisha Chemical Co., Ltd. Examples include meth)acrylate and epoxy(meth)acrylate manufactured by Nagase ChemteX.
• Examples of the epoxy (meth)acrylate manufactured by Daicel Allnex include EBECRYL860, EBECRYL3200, EBECRYL3201, EBECRYL3412, EBECRYL3600, EBECRYL3700, EBECRYL3701, EBECRYL3702, EBE Examples include CRYL3703, EBECRYL3708, EBECRYL3800, EBECRYL6040, EBECRYL RDX63182, KRM8342, and the like.
• Examples of the epoxy (meth)acrylate manufactured by Shin-Nakamura Chemical Industry Co., Ltd. include EA-1010, EA-1020, EA-5323, EA-5520, EA-CHD, and EMA-1020.
• Examples of the above-mentioned epoxy (meth)acrylate manufactured by Kyoeisha Chemical Co., Ltd. include Epoxy Ester M-600A, Epoxy Ester 40EM, Epoxy Ester 70PA, Epoxy Ester 200PA, Epoxy Ester 80MFA, Epoxy Ester 3002M, Epoxy Ester 3002A, Epoxy Ester 1600A, Examples include epoxy ester 3000M, epoxy ester 3000A, epoxy ester 200EA, and epoxy ester 400EA.
• Examples of the epoxy (meth)acrylate manufactured by Nagase ChemteX include Denacol Acrylate DA-141, Denacol Acrylate DA-314, Denacol Acrylate DA-911, and the like.
• the urethane (meth)acrylate can be obtained, for example, by reacting an isocyanate compound with a (meth)acrylic acid derivative having a hydroxyl group in the presence of a catalytic amount of a tin-based compound.
• isocyanate compound examples include isophorone diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, hexamethylene diisocyanate, trimethylhexamethylene diisocyanate, diphenylmethane-4,4'-diisocyanate (MDI), hydrogenated MDI, polymeric MDI, 1,5-naphthalene diisocyanate, norbornane diisocyanate, toridine diisocyanate, xylylene diisocyanate (XDI), hydrogenated XDI, lysine diisocyanate, triphenylmethane triisocyanate, tris(isocyanate phenyl) thiophosphate, tetramethyl xylylene diisocyanate Examples include isocyanate, 1,6,11-undecane triisocyanate, and the like.
• a chain-extended isocyanate compound obtained by reacting a polyol with an excess of an isocyanate compound can also be used.
• the polyol include ethylene glycol, propylene glycol, glycerin, sorbitol, trimethylolpropane, carbonate diol, polyether diol, polyester diol, polycaprolactone diol, and the like.
• Examples of the (meth)acrylic acid derivatives having a hydroxyl group include hydroxyalkyl mono(meth)acrylates, mono(meth)acrylates of dihydric alcohols, mono(meth)acrylates or di(meth)acrylates of trihydric alcohols. , epoxy (meth)acrylate, and the like.
• Examples of the hydroxyalkyl mono(meth)acrylate include 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 2-hydroxybutyl (meth)acrylate, and 4-hydroxybutyl (meth)acrylate. Can be mentioned.
• Examples of the dihydric alcohol include ethylene glycol, propylene glycol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, and polyethylene glycol.
• Examples of the trihydric alcohol include trimethylolethane, trimethylolpropane, and glycerin.
• Examples of the epoxy (meth)acrylate include bisphenol A type epoxy (meth)acrylate.
• urethane (meth)acrylates commercially available ones include, for example, urethane (meth)acrylate manufactured by Toagosei Co., Ltd., urethane (meth)acrylate manufactured by Daicel Ornex, and urethane (meth)acrylate manufactured by Negami Kogyo Co., Ltd.
• examples include acrylate, urethane (meth)acrylate manufactured by Shin-Nakamura Chemical Co., Ltd., and urethane (meth)acrylate manufactured by Kyoeisha Chemical Co., Ltd.
• Examples of the urethane (meth)acrylate manufactured by Toagosei Co., Ltd. include M-1100, M-1200, M-1210, and M-1600.
• Examples of the urethane (meth)acrylate manufactured by Daicel Allnex include EBECRYL210, EBECRYL220, EBECRYL230, EBECRYL270, EBECRYL1290, EBECRYL2220, EBECRYL4827, EBECRYL4842, EBECRY L4858, EBECRYL5129, EBECRYL6700, EBECRYL8402, EBECRYL8803, EBECRYL8804, EBECRYL8807, EBECRYL9260 etc. Can be mentioned. Examples of the urethane (meth)acrylate manufactured by Negami Kogyo Co., Ltd.
• Examples of the urethane (meth)acrylate manufactured by Kyoeisha Kagaku include AH-600, AI-600, AT-600, UA-101I, UA-101T, UA-306H, UA-306I, UA-306T, etc. It will be done.
• the (meth) When using a compound having an epoxy group and a compound having a (meth)acryloyl group as the curable resin, or when using a compound having an epoxy group and a (meth)acryloyl group, the (meth) ) It is preferable that the ratio of (meth)acryloyl groups in the total of acryloyl groups and epoxy groups is 30 mol % or more and 95 mol % or less. When the ratio of the (meth)acryloyl group is within this range, the resulting sealant for display elements has excellent adhesive properties and low liquid crystal contamination when used as a sealant for liquid crystal display elements.
• the sealant for display elements of the present invention contains a polymerization initiator.
• the polymerization initiator include radical polymerization initiators and cationic polymerization initiators.
• radical polymerization initiator a photo-radical polymerization initiator that generates radicals when irradiated with light or a thermal radical polymerization initiator that generates radicals when heated can be used.
• photoradical polymerization initiator examples include benzophenone compounds, acetophenone compounds, acylphosphine oxide compounds, titanocene compounds, oxime ester compounds, benzoin ether compounds, and thioxanthone compounds.
• photoradical polymerization initiator examples include 1-hydroxycyclohexylphenyl ketone, 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-1-butanone, 2-(dimethylamino )-2-((4-methylphenyl)methyl)-1-(4-(4-morpholinyl)phenyl)-1-butanone, 2,2-dimethoxy-1,2-diphenylethan-1-one, bis( 2,4,6-trimethylbenzoyl)phenylphosphine oxide, 2-methyl-1-(4-methylthiophenyl)-2-morpholinopropan-1-one, 1-(4-(2-hydroxyethoxy)-phenyl) -2-hydroxy-2-methyl-1-propan-1-one, 1-(4-(phenylthio)phenyl)-1,2-octanedione 2-(O-benzoyloxime), 2,4,6-trimethyl Examples include benzoyldiphenylphosphin
• thermal radical polymerization initiator examples include those composed of azo compounds, organic peroxides, and the like.
• initiators composed of azo compounds (hereinafter also referred to as “azo initiators”) are used from the viewpoint of low liquid crystal contamination when the obtained sealant for display elements is used as a sealant for liquid crystal display elements.
• an initiator composed of a polymer azo compound (hereinafter also referred to as a "polymer azo initiator”) is more preferable.
• the thermal radical polymerization initiators may be used alone or in combination of two or more.
• polymeric azo compound means a compound having an azo group and generating a radical capable of reacting a (meth)acryloyl group with heat, and having a number average molecular weight of 300 or more. do.
• the preferable lower limit of the number average molecular weight of the polymeric azo compound is 1,000, and the preferable upper limit is 300,000.
• the number average molecular weight of the polymeric azo compound is within this range, it can be easily mixed into the curable resin while preventing an adverse effect on the liquid crystal.
• a more preferable lower limit of the number average molecular weight of the polymer azo compound is 5,000, a more preferable upper limit is 100,000, an even more preferable lower limit is 10,000, and an even more preferable upper limit is 90,000.
• the said number average molecular weight is the value calculated
• Examples of the above-mentioned polymeric azo compounds include those having a structure in which a plurality of units such as polyalkylene oxide and polydimethylsiloxane are bonded via an azo group.
• the polymeric azo compound having a structure in which a plurality of units such as polyalkylene oxide are bonded via an azo group is preferably one having a polyethylene oxide structure.
• Specific examples of the above-mentioned polymer azo compounds include polycondensates of 4,4'-azobis(4-cyanopentanoic acid) and polyalkylene glycol, and 4,4'-azobis(4-cyanopentanoic acid).
• Examples include polycondensates of polydimethylsiloxane and polydimethylsiloxane having terminal amino groups.
• polymeric azo initiators commercially available ones include, for example, VPE-0201, VPE-0401, VPE-0601, VPS-0501, and VPS-1001 (all manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.). Can be mentioned.
• non-polymer azo initiators include V-65 and V-501 (both manufactured by Fuji Film Wako Pure Chemical Industries, Ltd.).
• organic peroxide examples include ketone peroxide, peroxyketal, hydroperoxide, dialkyl peroxide, peroxy ester, diacyl peroxide, peroxydicarbonate, and the like.
• a photocationic polymerization initiator As the cationic polymerization initiator, a photocationic polymerization initiator is suitably used.
• the photocationic polymerization initiator is not particularly limited as long as it generates a protonic acid or a Lewis acid when irradiated with light, and may be an ionic photoacid generating type or a nonionic photoacid generating type. It may be.
• photocationic polymerization initiator examples include onium salts such as aromatic diazonium salts, aromatic halonium salts, and aromatic sulfonium salts, organometallic complexes such as iron-arene complexes, titanocene complexes, and arylsilanol-aluminum complexes. can be mentioned.
• photocationic polymerization initiators examples include Adeka Optomer SP-150 and Adeka Optomer SP-170 (both manufactured by ADEKA).
• the content of the polymerization initiator has a preferable lower limit of 0.01 parts by weight and a preferable upper limit of 10 parts by weight based on 100 parts by weight of the curable resin.
• the obtained sealant for display elements has better storage stability and curability, and also reduces liquid crystal contamination when used as a sealant for liquid crystal display elements. It will be better due to its properties.
• a more preferable lower limit of the content of the polymerization initiator is 0.1 parts by weight, and a more preferable upper limit is 5 parts by weight.
• the sealant for display elements of the present invention contains a thermosetting agent.
• the thermosetting agent include organic acid hydrazides, imidazole derivatives, amine compounds, polyhydric phenol compounds, and acid anhydrides. Among them, organic acid hydrazides are preferably used.
• the above thermosetting agents may be used alone or in combination of two or more.
• Examples of the organic acid hydrazide include sebacic acid dihydrazide, isophthalic acid dihydrazide, adipic acid dihydrazide, malonic acid dihydrazide, and the like.
• Examples of commercially available organic acid hydrazides include organic acid hydrazides manufactured by Otsuka Chemical Co., Ltd. and organic acid hydrazides manufactured by Ajinomoto Fine Techno.
• Examples of the organic acid hydrazides manufactured by Otsuka Chemical include SDH, ADH, MDH, and the like.
• Examples of the organic acid hydrazide manufactured by Ajinomoto Fine Techno include Amicure VDH, Amicure VDH-J, Amicure UDH, and Amicure UDH-J.
• the preferable lower limit of the content of the thermosetting agent is 1 part by weight and the preferable upper limit is 50 parts by weight based on 100 parts by weight of the curable resin.
• the content of the thermosetting agent is within this range, the resulting sealant for display elements can have better thermosetting properties without deteriorating the applicability or the like.
• a more preferable upper limit of the content of the thermosetting agent is 30 parts by weight.
• the sealant for display elements of the present invention may contain a filler for the purpose of improving viscosity, further improving adhesiveness due to stress dispersion effect, improving coefficient of linear expansion, further improving moisture resistance of cured product, etc. is preferred.
• an inorganic filler or an organic filler can be used as the filler.
• the inorganic fillers include silica, talc, glass beads, asbestos, gypsum, diatomaceous earth, smectite, bentonite, montmorillonite, sericite, activated clay, alumina, zinc oxide, iron oxide, magnesium oxide, tin oxide, and titanium oxide. , calcium carbonate, magnesium carbonate, magnesium hydroxide, aluminum hydroxide, aluminum nitride, silicon nitride, barium sulfate, calcium silicate, and the like.
• the organic filler include polyester fine particles, polyurethane fine particles, vinyl polymer fine particles, and acrylic polymer fine particles. The above fillers may be used alone or in combination of two or more.
• the preferable lower limit of the content of the filler in 100 parts by weight of the display element sealant of the present invention is 10 parts by weight, and the preferable upper limit is 70 parts by weight.
• the content of the filler is within this range, the adhesiveness can be improved without deteriorating the coating properties and the like.
• a more preferable lower limit of the content of the filler is 20 parts by weight, and a more preferable upper limit is 60 parts by weight.
• the display element sealant of the present invention may contain a silane coupling agent.
• the silane coupling agent mainly serves as an adhesion aid for adhering the sealant and the substrate etc. well.
• silane coupling agent for example, 3-aminopropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-isocyanatepropyltrimethoxysilane, etc. are preferably used. These are excellent in the effect of improving adhesiveness with substrates, etc., and can suppress the outflow of the curable resin into the liquid crystal by chemically bonding with the curable resin.
• the above-mentioned silane coupling agents may be used alone, or two or more types may be used in combination.
• the preferable lower limit of the content of the silane coupling agent in 100 parts by weight of the display element sealant of the present invention is 0.1 parts by weight, and the preferable upper limit is 10 parts by weight.
• the content of the silane coupling agent is within this range, it has an excellent effect of improving adhesiveness, and also has an excellent low liquid crystal staining property when used as a sealant for a liquid crystal display element.
• a more preferable lower limit of the content of the silane coupling agent is 0.3 parts by weight, and a more preferable upper limit is 5 parts by weight.
• the display element sealant of the present invention may contain a light shielding agent.
• the display element sealant of the present invention can be suitably used as a light-shielding sealant.
• Examples of the light shielding agent include iron oxide, titanium black, aniline black, cyanine black, fullerene, carbon black, and resin-coated carbon black. Among them, titanium black is preferred.
• the titanium black is a material that has a higher transmittance for light in the vicinity of the ultraviolet region, particularly for light with a wavelength of 370 nm or more and 450 nm or less, compared to an average transmittance for light with a wavelength of 300 nm or more and 800 nm or less. That is, the titanium black has the property of imparting light-shielding properties to the display element sealant of the present invention by sufficiently blocking light with wavelengths in the visible light region, while allowing light with wavelengths near the ultraviolet region to pass through. It is a light blocking agent.
• the display of the present invention can be achieved.
• the photocurability of the element sealant can be further increased.
• the light shielding agent contained in the display element sealant of the present invention is preferably a highly insulating substance, and titanium black is also suitable as a highly insulating light shielding agent.
• the optical density (OD value) per 1 ⁇ m of the titanium black is preferably 3 or more, more preferably 4 or more. The higher the light-shielding property of the titanium black, the better. There is no particular upper limit to the OD value of the titanium black, but it is usually 5 or less.
• the titanium black mentioned above exhibits sufficient effects even if it is not surface-treated, but it may also be used if the surface is treated with an organic component such as a coupling agent, silicon oxide, titanium oxide, germanium oxide, aluminum oxide, etc.
• an organic component such as a coupling agent, silicon oxide, titanium oxide, germanium oxide, aluminum oxide, etc.
• Surface-treated titanium black such as one coated with an inorganic component such as zirconium or magnesium oxide, can also be used.
• those treated with organic components are preferable because they can further improve insulation properties.
• display elements manufactured using the sealant for display elements of the present invention containing the titanium black as a light shielding agent have sufficient light shielding properties, so there is no light leakage, high contrast, and excellent A display element having high image display quality can be realized.
• Examples of commercially available titanium blacks include titanium black manufactured by Mitsubishi Materials, titanium black manufactured by Ako Kasei, and the like. Examples of the titanium black manufactured by Mitsubishi Materials include 12S, 13M, 13MC, 13R-N, and 14MC. Examples of the titanium black manufactured by Ako Kasei Co., Ltd. include TILAC D and the like.
• the preferable lower limit of the specific surface area of the titanium black is 13 m 2 /g, the preferable upper limit is 30 m 2 /g, the more preferable lower limit is 15 m 2 /g, and the more preferable upper limit is 25 m 2 /g.
• a preferable lower limit of the volume resistivity of the titanium black is 0.5 ⁇ cm, a preferable upper limit is 3 ⁇ cm, a more preferable lower limit is 1 ⁇ cm, and a more preferable upper limit is 2.5 ⁇ cm.
• the primary particle diameter of the light shielding agent is not particularly limited as long as it is equal to or less than the distance between the substrates of the display element, but the preferable lower limit is 1 nm and the preferable upper limit is 5000 nm. When the primary particle diameter of the light shielding agent is within this range, the resulting sealant for display elements can have better light shielding properties without deteriorating the applicability or the like.
• a more preferable lower limit of the primary particle diameter of the light shielding agent is 5 nm, a more preferable upper limit is 200 nm, an even more preferable lower limit is 10 nm, and an even more preferable upper limit is 100 nm.
• the primary particle size of the light shielding agent can be measured by dispersing the light shielding agent in a solvent (water, organic solvent, etc.) using NICOMP 380ZLS (manufactured by PARTICLE SIZING SYSTEMS).
• the preferable lower limit of the content of the light shielding agent in 100 parts by weight of the display element sealant of the present invention is 5 parts by weight, and the preferable upper limit is 80 parts by weight.
• the resulting sealant for display elements exhibits superior light-shielding properties without greatly reducing the adhesiveness, strength after curing, and drawing properties. Can be done.
• a more preferable lower limit of the content of the light blocking agent is 10 parts by weight, a more preferable upper limit is 70 parts by weight, an even more preferable lower limit is 30 parts by weight, and an even more preferable upper limit is 60 parts by weight.
• the sealant for display elements of the present invention may further contain additives such as a stress relaxation agent, a reactive diluent, a thixotropic agent, a spacer, a curing accelerator, an antifoaming agent, a leveling agent, and a polymerization inhibitor, as necessary. May contain.
• a curable resin is mixed with a polymerization initiator, a thermosetting agent, a silane coupling agent, etc. added as necessary, using a mixer.
• a mixer include a method to do so.
• the mixer include a homodisper, a homomixer, a universal mixer, a planetary mixer, a kneader, and a three-roll mixer.
• a vertically conductive material can be manufactured.
• conductive fine particles for example, metal balls, resin fine particles with a conductive metal layer formed on the surface, etc. can be used.
• resin fine particles with a conductive metal layer formed on the surface are preferable because the excellent elasticity of the resin fine particles allows conductive connection without damaging the transparent substrate or the like.
• the display element sealant of the present invention is suitably used as a liquid crystal display element sealant.
• a sealant for liquid crystal display elements using the sealant for display elements of the present invention is also one of the aspects of the present invention.
• a liquid crystal display element having a cured product of the sealant for liquid crystal display element of the present invention is also one of the present invention.
• a liquid crystal display element with a narrow frame design is preferable. Specifically, it is preferable that the width of the frame portion around the liquid crystal display section is 2 mm or less. Moreover, it is preferable that the coating width of the sealant for a liquid crystal display element of the present invention when manufacturing the liquid crystal display element of the present invention is 1 mm or less.
• the sealant for liquid crystal display elements of the present invention can be suitably used for manufacturing liquid crystal display elements by the liquid crystal dropping method.
• Examples of the method for manufacturing the liquid crystal display element of the present invention using the liquid crystal dropping method include the following method. First, a step of forming a frame-shaped seal pattern on a substrate with the sealant for liquid crystal display elements of the present invention by screen printing, dispenser application, etc. is performed. Next, with the sealant for liquid crystal display elements of the present invention in an uncured state, fine droplets of liquid crystal are applied dropwise to the entire area within the frame of the seal pattern, and immediately another substrate is superimposed. Thereafter, a liquid crystal display element can be obtained by a method of performing a step of heating and curing the sealant. Further, before the step of heating and curing the sealant, a step of temporarily curing the sealant by irradiating the seal pattern portion with light such as ultraviolet rays may be performed.
• a sealant for a display element that is excellent in flexibility responsiveness, adhesiveness to an alignment film, adhesiveness in a high temperature and high humidity environment, and moisture permeation prevention property. Further, according to the present invention, it is possible to provide a sealant for a liquid crystal display element and a liquid crystal display element using the sealant for a display element.
• the obtained product was washed three times with 100 mL of water to obtain 28 g of curable resin A as a yellow viscous substance.
• the obtained curable resin A is a compound represented by the above formula (1) (R 1 and R 2 are represented by the above formula (2-2)). It was confirmed that X is a structure represented by the following formula (4), and Y is a structure represented by the above formula (3) (R 4 and R 5 are hydrogen atoms).
• curable resin D 18 g of curable resin D was obtained in the same manner as in "(Preparation of curable resin A)" above, except that 23 g of hexadecanedioic acid (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was used in place of 34 g of eicosandioic acid.
• 1 H-NMR, GPC, and FT-IR the obtained curable resin D is a compound represented by the above formula (1) (R 1 and R 2 are represented by the above formula (2-2)). It was confirmed that X is a structure represented by the following formula (7), and Y is a structure represented by the above formula (3) (R 4 and R 5 are hydrogen atoms).
• * represents the bonding position
• curable resin E 24 g of curable resin E was obtained in the same manner as in "(Preparation of curable resin A)" above, except that 28 g of dodecanedioic acid (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was used in place of 34 g of eicosandioic acid.
• 1 H-NMR, GPC, and FT-IR the obtained curable resin E is a compound represented by the above formula (1) (R 1 and R 2 are represented by the above formula (2-2)). It was confirmed that X is a structure represented by the following formula (8), and Y is a structure represented by the above formula (3) (R 4 and R 5 are hydrogen atoms).
• curable resin H 20 g of curable resin H was obtained in the same manner as in "(Preparation of curable resin A)" above, except that 74 g of bisphenol E diglycidyl ether (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was used in place of 72 g of bisphenol F diglycidyl ether.
• the obtained curable resin H is a compound represented by the above formula (1) (R 1 and R 2 are represented by the above formula (2-2)).
• curable resin I 20 g of curable resin I was obtained in the same manner as in "(Preparation of curable resin A)" above, except that 52 g of resorcinol diglycidyl ether (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was used in place of 72 g of bisphenol F diglycidyl ether. .
• the obtained curable resin I is a compound represented by the above formula (1) (R 1 and R 2 are represented by the above formula (2-2)). It was confirmed that X is a structure represented by the above formula (4), and Y is a 1,3-phenylene group.
• the obtained curable resin J is a compound represented by the above formula (1) (R 1 and R 2 are represented by the above formula (2-1)). It was confirmed that X is a structure represented by the above formula (4), and Y is a structure represented by the above formula (3) (R 4 and R 5 are hydrogen atoms).
• curable resin L 8 g of curable resin L was obtained in the same manner as in "(Preparation of curable resin A)" above, except that 10 g of succinic anhydride (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was used in place of 34 g of eicosandioic acid.
• the curable resin L obtained by 1 H-NMR, GPC, and FT-IR has a structure in which the portions corresponding to R 1 and R 2 in the above formula (1) are represented by the above formula (2-2).
• the compound was confirmed to be a compound in which the group corresponding to X, the part corresponding to X is a dimethylene group, and the part corresponding to Y all has a structure represented by the above formula (3) (R 4 and R 5 are hydrogen atoms).
• curable resin M 20 g of curable resin M was obtained in the same manner as in "(Preparation of curable resin A)" above, except that 26 g of tetracosane dioic acid (manufactured by BOC Sciences) was used in place of 34 g of eicosane dioic acid.
• the curable resin M obtained by 1 H-NMR, GPC, and FT-IR has a structure in which the portions corresponding to R 1 and R 2 in the above formula (1) are represented by the above formula (2-2). group , a structure in which the part corresponding to It was confirmed that it was a compound.
• Examples 1 to 13, Comparative Examples 1 to 3 According to the compounding ratios listed in Tables 1 and 2, each material was mixed using a planetary stirrer (manufactured by Shinky Co., Ltd., "Awatori Rentaro"), and then further mixed using three rolls. Sealants for display elements of Examples 1 to 13 and Comparative Examples 1 to 3 were prepared.
• Each of the display element sealants obtained in Examples and Comparative Examples was irradiated with ultraviolet rays (wavelength 365 nm) at 100 mW/cm 2 for 30 seconds using a metal halide lamp, and then heated at 120° C. for 1 hour to give a thickness of 500 ⁇ m.
• a film was prepared and designated as test piece 1.
• Each of the obtained test pieces was wrapped around a SUS rod having a diameter of 30 mm and fixed with adhesive tape ("Cloth Tape 601S", manufactured by Sekisui Chemical Co., Ltd.), and the condition of each test piece was visually observed. As a result, the case where no peeling between the test piece 1 and the adhesive tape was confirmed was evaluated as "A".
• Spacer fine particles 1 part by weight of spacer fine particles was dispersed in 100 parts by weight of each display element sealant obtained in Examples and Comparative Examples.
• spacer fine particles Micropearl SI-H050 (manufactured by Sekisui Chemical Co., Ltd.) was used.
• a sealant for display elements in which fine spacer particles were dispersed was applied to one of the two glass substrates (length 30 mm, width 60 mm) with polyimide alignment films for TN (manufactured by Nissan Chemical Co., Ltd., "SE6414"). dripped.
• the other glass substrate with a polyimide alignment film for TN was bonded to this in a cross shape, irradiated with ultraviolet rays of 3000 mJ/cm 2 using a metal halide lamp, and then heated at 120°C for 60 minutes to obtain an adhesive test piece.
• Ta The strength at which panel peeling occurred was measured when the edge of the substrate in the prepared adhesive test piece was pushed in at a speed of 5 mm/min using a metal cylinder with a radius of 5 mm. If the value obtained by dividing the obtained measured value (kgf) by the seal diameter (cm) was 3.0 kgf/cm or more, it was "A", and it was 2.5 kgf/cm or more and less than 3.0 kgf/cm.
• the adhesion to the alignment film was evaluated as "B” if it was more than 2.0 kgf/cm and less than 2.5 kgf/cm, and "D” if it was less than 2.0 kgf/cm. did.
• Adhesion after high temperature and high humidity test (adhesion under high temperature and high humidity environment)) An adhesive test piece was obtained in the same manner as in "(Adhesion to alignment film)" above. A high temperature and high humidity test was conducted in which the obtained adhesive test piece was exposed to 121° C., 100% RH, and 2 atm for 12 hours. After the high temperature and high humidity test, the edge of the substrate in the adhesive test piece was pushed in at a speed of 5 mm/min using a metal cylinder with a radius of 5 mm, and the strength at which panel peeling occurred was measured.
• Each of the display element sealants obtained in Examples and Comparative Examples was applied onto a smooth release film using a coater to a thickness of 200 to 300 ⁇ m. Next, after irradiating with ultraviolet rays of 3000 mJ/cm 2 using a metal halide lamp, the sealant was cured by heating at 120° C. for 1 hour to obtain a film for moisture permeability measurement.
• a moisture permeability test cup was prepared in accordance with the JIS Z 0208 moisture permeability test method for moisture-proof packaging materials (cup method), the resulting moisture permeability measurement film was attached, and the cup was kept at a constant temperature of 60°C and 90% RH. The moisture permeability was measured by placing it in a wet oven.
• A indicates that the obtained moisture permeability value is 50 g/ m 2.24 hr or less; "B” indicates that it exceeds 50 g/m 2.24 hr and does not exceed 60 g/m 2.24 hr; 60 g Moisture permeation prevention property was evaluated as “C” when it exceeded 70 g/m 2.24 hr and less than 70 g/m 2.24 hr, and as “D " when it exceeded 70 g/m 2.24 hr.
• a sealant for a display element that is excellent in flexibility responsiveness, adhesiveness to an alignment film, adhesiveness in a high temperature and high humidity environment, and moisture permeation prevention property. Further, according to the present invention, it is possible to provide a sealant for a liquid crystal display element and a liquid crystal display element using the sealant for a display element.

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