TWI707912B - Sealant for liquid crystal display element, vertical conduction material, and liquid crystal display element - Google Patents

Sealant for liquid crystal display element, vertical conduction material, and liquid crystal display element Download PDF

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TWI707912B
TWI707912B TW105132132A TW105132132A TWI707912B TW I707912 B TWI707912 B TW I707912B TW 105132132 A TW105132132 A TW 105132132A TW 105132132 A TW105132132 A TW 105132132A TW I707912 B TWI707912 B TW I707912B
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meth
acrylate
liquid crystal
crystal display
epoxy
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TW201726803A (en
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松井慶枝
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日商積水化學工業股份有限公司
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/10Materials in mouldable or extrudable form for sealing or packing joints or covers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/46Polymerisation initiated by wave energy or particle radiation
    • C08F2/48Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
    • C08F2/50Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/26Esters containing oxygen in addition to the carboxy oxygen
    • C08F220/32Esters containing oxygen in addition to the carboxy oxygen containing epoxy radicals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates 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
    • C08G59/18Macromolecules 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
    • C08G59/20Macromolecules 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
    • 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
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1339Gaskets; Spacers; Sealing of cells
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2200/00Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
    • C09K2200/04Non-macromolecular organic compounds
    • C09K2200/0441Carboxylic acids, salts, anhydrides or esters thereof

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  • Physics & Mathematics (AREA)
  • Organic Chemistry (AREA)
  • Polymers & Plastics (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
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  • Mathematical Physics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Sealing Material Composition (AREA)
  • Liquid Crystal (AREA)

Abstract

本發明之目的在於提供一種光硬化性、接著性、及防透濕性優異之液晶顯示元件用密封劑。又,本發明之目的在於提供一種使用該液晶顯示元件用密封劑而形成之上下導通材料及液晶顯示元件。 The object of the present invention is to provide a sealing compound for liquid crystal display elements that is excellent in photocurability, adhesiveness, and moisture permeability. In addition, an object of the present invention is to provide a liquid crystal display element and an upper and lower conduction material formed by using the sealing compound for liquid crystal display elements.

本發明係一種液晶顯示元件用密封劑,其含有1分子中具有1個以上之(甲基)丙烯醯基之環氧(甲基)丙烯酸酯、1分子中具有1個以上之環氧基之環氧化合物、及1分子中具有2個以上之順丁烯二醯亞胺基之多官能順丁烯二醯亞胺化合物,且上述環氧(甲基)丙烯酸酯與上述環氧化合物之合計100重量份中之上述環氧(甲基)丙烯酸酯之含量超過50重量份且為90重量份以下。 The present invention is a sealing compound for liquid crystal display elements, which contains epoxy (meth)acrylate having one or more (meth)acrylic groups in one molecule, and one having one or more epoxy groups in one molecule An epoxy compound, and a multifunctional maleimide compound having two or more maleimide groups in one molecule, and the sum of the above-mentioned epoxy (meth)acrylate and the above-mentioned epoxy compound The content of the epoxy (meth)acrylate in 100 parts by weight exceeds 50 parts by weight and is 90 parts by weight or less.

Description

液晶顯示元件用密封劑、上下導通材料、及液晶顯示元件 Sealant for liquid crystal display element, vertical conduction material, and liquid crystal display element

本發明關於一種光硬化性、接著性、及防透濕性優異之液晶顯示元件用密封劑。又,本發明係關於一種使用該液晶顯示元件用密封劑而成之上下導通材料及液晶顯示元件。 The present invention relates to a sealing compound for liquid crystal display elements having excellent photocurability, adhesiveness, and moisture permeability. In addition, the present invention relates to an upper and lower conduction material and a liquid crystal display element using this sealant for liquid crystal display elements.

近年來,關於液晶顯示單元等液晶顯示元件之製造方法,就工站時間(tact time)縮短、使用液晶量之最佳化等觀點而言,主流方法係自習知之真空注入方式變成例如如專利文獻1、專利文獻2所揭示之使用光熱併用硬化型密封劑的被稱為滴下法之液晶滴下方式。 In recent years, regarding the manufacturing method of liquid crystal display elements such as liquid crystal display units, from the viewpoints of shortening tact time and optimizing the amount of liquid crystal used, the mainstream method is a self-known vacuum injection method. 1. The liquid crystal dropping method called the dropping method that uses light and heat in combination with a hardening type sealant disclosed in Patent Document 2.

於滴下法中,首先藉由點膠機(dispense)於2片附電極之透明基板之一片形成長方形狀之密封圖案。繼而,於密封劑未硬化之狀態下對透明基板之框內整個面滴下液晶之微小液滴,立即與另一片透明基板重合,對密封部照射紫外線等光而進行暫時硬化。之後,於液晶退火時進行加熱而進行正式硬化,而製作液晶顯示元件。只要於減壓下進行基板之貼合,則可以極高之效率製造液晶顯示元件。 In the dropping method, a rectangular seal pattern is first formed on one of two transparent substrates with electrodes by a dispenser. Then, in a state where the sealant is not hardened, small droplets of liquid crystal are dropped on the entire surface of the frame of the transparent substrate, immediately overlap with another transparent substrate, and the sealing part is irradiated with light such as ultraviolet rays to temporarily harden. After that, heating is performed during liquid crystal annealing to perform main curing, and a liquid crystal display element is produced. As long as the substrates are bonded under reduced pressure, liquid crystal display elements can be manufactured with extremely high efficiency.

伴隨著平板(tablet)終端或行動終端之普及,對於液晶顯示元件,逐漸要求於高溫高濕環境下之驅動等時的耐濕可靠性,對於密封 劑,進一步要求防止水自外部滲入之性能。為了提高液晶顯示元件之耐濕可靠性,必須提高密封劑與基板等之接著性,且使密封劑之硬化物成為防透濕性優異者。然而,關於密封劑,兼顧接著性及防透濕性較為困難。 With the popularization of tablet terminals or mobile terminals, liquid crystal display elements are gradually required to have humidity resistance reliability when driving in a high temperature and high humidity environment. It is further required to prevent water from penetrating from the outside. In order to improve the moisture resistance reliability of the liquid crystal display element, it is necessary to improve the adhesiveness of the sealant to the substrate, etc., and to make the cured product of the sealant have excellent moisture permeability. However, it is difficult for the sealant to have both adhesiveness and moisture permeability resistance.

專利文獻1:日本特開2001-133794號公報 Patent Document 1: Japanese Patent Application Publication No. 2001-133794

專利文獻2:日本特開平5-295087號公報 Patent Document 2: Japanese Patent Application Publication No. 5-295087

本發明係關於一種光硬化性、接著性、及防透濕性優異之液晶顯示元件用密封劑。又,本發明之目的在於提供一種使用該液晶顯示元件用密封劑而成之上下導通材料及液晶顯示元件。 The present invention relates to a sealing compound for liquid crystal display elements having excellent photocurability, adhesiveness, and moisture permeability. In addition, an object of the present invention is to provide an upper and lower conduction material and a liquid crystal display element using this sealing compound for liquid crystal display elements.

本發明係一種液晶顯示元件用密封劑,其含有1分子中具有1個以上之(甲基)丙烯醯基之環氧(甲基)丙烯酸酯、1分子中具有1個以上之環氧基之環氧化合物、及1分子中具有2個以上之順丁烯二醯亞胺基之多官能順丁烯二醯亞胺化合物,且上述環氧(甲基)丙烯酸酯與上述環氧化合物之合計100重量份中之上述環氧(甲基)丙烯酸酯之含量超過50重量份且為90重量份以下。 The present invention is a sealing compound for liquid crystal display elements, which contains epoxy (meth)acrylate having one or more (meth)acrylic groups in one molecule, and one having one or more epoxy groups in one molecule An epoxy compound, and a multifunctional maleimide compound having two or more maleimide groups in one molecule, and the sum of the above-mentioned epoxy (meth)acrylate and the above-mentioned epoxy compound The content of the epoxy (meth)acrylate in 100 parts by weight exceeds 50 parts by weight and is 90 parts by weight or less.

以下,對本發明詳細進行說明。 Hereinafter, the present invention will be described in detail.

本發明人進行了如下研究:藉由使含有(甲基)丙烯酸化合物及環氧化合物之液晶顯示元件用密封劑進而含有多官能順丁烯二醯亞胺化 合物,而提高該液晶顯示元件用密封劑之防透濕性。然而,所獲得之液晶顯示元件用密封劑存在光硬化性或接著性不充分之問題。因此,本發明人發現,藉由進而使用環氧(甲基)丙烯酸酯作為(甲基)丙烯酸化合物,並將該環氧(甲基)丙烯酸酯之含量設為特定之範圍內,而可獲得了光硬化性、接著性、及防透濕性優異之液晶顯示元件用密封劑,從而完成本發明。又,藉由使用本發明之液晶顯示元件用密封劑,亦可抑制液晶污染。 The inventors of the present invention conducted the following studies: by making a sealing compound for liquid crystal display elements containing a (meth)acrylic compound and an epoxy compound and further containing a polyfunctional maleimide Compound, and improve the moisture permeability of the sealing compound for liquid crystal display elements. However, the obtained sealing compound for liquid crystal display elements has the problem of insufficient photocurability or adhesiveness. Therefore, the inventors found that by further using epoxy (meth)acrylate as the (meth)acrylic compound and setting the content of the epoxy (meth)acrylate within a specific range, it is possible to obtain The present invention has been completed by providing a sealing compound for liquid crystal display elements having excellent photocuring properties, adhesiveness, and moisture permeability resistance. Moreover, by using the sealing compound for liquid crystal display elements of this invention, liquid crystal contamination can also be suppressed.

再者,於本說明書中,上述「(甲基)丙烯酸」意指丙烯酸或甲基丙烯酸,上述「(甲基)丙烯酸酯」意指丙烯酸酯或甲基丙烯酸酯,上述「環氧(甲基)丙烯酸酯」表示使環氧化合物中之環氧基與(甲基)丙烯酸進行反應而成之化合物。 Furthermore, in this specification, the above-mentioned "(meth)acrylic acid" means acrylic acid or methacrylic acid, the above-mentioned "(meth)acrylate" means acrylate or methacrylate, and the above-mentioned "epoxy (methyl) )Acrylate" means a compound formed by reacting an epoxy group in an epoxy compound with (meth)acrylic acid.

本發明之液晶顯示元件用密封劑含有1分子中具有1個以上之(甲基)丙烯醯基之環氧(甲基)丙烯酸酯。 The sealing compound for liquid crystal display elements of this invention contains the epoxy (meth)acrylate which has 1 or more (meth)acryl group in 1 molecule.

再者,於本說明書中,上述「(甲基)丙烯醯基」意指丙烯醯基或甲基丙烯醯基。又,上述環氧(甲基)丙烯酸酯並不限定於使環氧化合物中之全部環氧基與(甲基)丙烯酸進行反應而成之化合物,如下述般,部分(甲基)丙烯酸改質環氧樹脂亦包含於上述環氧(甲基)丙烯酸酯中。 In addition, in this specification, the above-mentioned "(meth)acryl group" means an acrylic group or a methacryl group. In addition, the above-mentioned epoxy (meth)acrylate is not limited to a compound obtained by reacting all epoxy groups in an epoxy compound with (meth)acrylic acid. As described below, part of (meth)acrylic acid is modified The epoxy resin is also contained in the above-mentioned epoxy (meth)acrylate.

上述環氧(甲基)丙烯酸酯就反應性之高低而言,較佳為1分子中具有2個以上之(甲基)丙烯醯基者。 The epoxy (meth)acrylate is preferably one having two or more (meth)acrylic groups in one molecule in terms of the level of reactivity.

作為上述環氧(甲基)丙烯酸酯,例如可列舉:藉由按照常用方法於鹼性觸媒之存在下使環氧化合物與(甲基)丙烯酸進行反應而獲得者等。 As said epoxy (meth)acrylate, the thing obtained by reacting an epoxy compound and (meth)acrylic acid in the presence of a basic catalyst according to a common method, etc. are mentioned, for example.

作為成為用以合成上述環氧(甲基)丙烯酸酯之原料之環氧 化合物,例如可列舉:雙酚A型環氧樹脂、雙酚F型環氧樹脂、雙酚S型環氧樹脂、2,2'-二烯丙基雙酚A型環氧樹脂、氫化雙酚型環氧樹脂、環氧丙烷加成雙酚A型環氧樹脂、間苯二酚型環氧樹脂、聯苯型環氧樹脂、硫醚(sulfide)型環氧樹脂、二苯醚型環氧樹脂、二環戊二烯型環氧樹脂、萘型環氧樹脂、苯酚酚醛清漆型環氧樹脂、鄰甲酚酚醛清漆型環氧樹脂、二環戊二烯酚醛清漆型環氧樹脂、聯苯酚醛清漆型環氧樹脂、萘酚酚醛清漆型環氧樹脂、縮水甘油胺型環氧樹脂、烷基多元醇型環氧樹脂、橡膠改質型環氧樹脂、縮水甘油酯化合物等。 As a raw material for synthesizing the above epoxy (meth)acrylate Examples of the compound include: bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol S type epoxy resin, 2,2'-diallyl bisphenol A type epoxy resin, hydrogenated bisphenol Type epoxy resin, propylene oxide addition bisphenol A type epoxy resin, resorcinol type epoxy resin, biphenyl type epoxy resin, sulfide type epoxy resin, diphenyl ether type epoxy resin Resin, dicyclopentadiene type epoxy resin, naphthalene type epoxy resin, phenol novolak type epoxy resin, o-cresol novolak type epoxy resin, dicyclopentadiene novolak type epoxy resin, biphenol Aldehyde type epoxy resin, naphthol novolak type epoxy resin, glycidylamine type epoxy resin, alkyl polyol type epoxy resin, rubber modified type epoxy resin, glycidyl ester compound, etc.

作為上述雙酚A型環氧樹脂中之市售品,例如可列舉:jER 828EL、jER 1004(均為三菱化學公司製造)、EPICLON 850(DIC公司製造)等。 Examples of commercially available products among the above-mentioned bisphenol A epoxy resins include jER 828EL, jER 1004 (all manufactured by Mitsubishi Chemical Corporation), EPICLON 850 (manufactured by DIC Corporation), and the like.

作為上述雙酚F型環氧樹脂中之市售品,例如可列舉:jER 806、jER 4004(均為三菱化學公司製造)等。 As a commercial item among the said bisphenol F type epoxy resin, jER 806, jER 4004 (all are manufactured by Mitsubishi Chemical Corporation) etc. are mentioned, for example.

作為上述雙酚S型環氧樹脂中之市售品,例如可列舉:EPICLON EXA1514(DIC公司製造)等。 As a commercial item among the said bisphenol S-type epoxy resin, EPICLON EXA1514 (made by DIC Corporation) etc. are mentioned, for example.

作為上述2,2'-二烯丙基雙酚A型環氧樹脂中之市售品,例如可列舉:RE-810NM(日本化藥公司製造)等。 As a commercial item among the said 2,2'-diallyl bisphenol A type epoxy resin, RE-810NM (made by Nippon Kayaku Co., Ltd.) etc. are mentioned, for example.

作為上述氫化雙酚型環氧樹脂中之市售品,例如可列舉:EPICLON EXA 7015(DIC公司製造)等。 As a commercial item among the said hydrogenated bisphenol type epoxy resin, EPICLON EXA 7015 (made by DIC Corporation) etc. are mentioned, for example.

作為上述環氧丙烷加成雙酚A型環氧樹脂中之市售品,例如可列舉:EP-4000S(ADEKA公司製造)等。 As a commercial item among the said propylene oxide addition bisphenol A type epoxy resin, EP-4000S (made by ADEKA company) etc. are mentioned, for example.

作為上述間苯二酚型環氧樹脂中之市售品,例如可列舉:EX-201 (Nagase chemteX公司製造)等。 Examples of commercially available products among the above resorcinol type epoxy resins include: EX-201 (Manufactured by Nagase chemteX) and so on.

作為上述聯苯型環氧樹脂中之市售品,例如可列舉:jER YX-4000H(三菱化學公司製造)等。 As a commercial item among the said biphenyl type epoxy resin, jER YX-4000H (made by Mitsubishi Chemical Corporation) etc. are mentioned, for example.

作為上述硫醚型環氧樹脂中之市售品,例如可列舉:YSLV-50TE(新日鐵住金化學公司製造)等。 Examples of commercially available products among the above-mentioned sulfide-type epoxy resins include YSLV-50TE (manufactured by Nippon Steel & Sumikin Chemical Co., Ltd.).

作為上述二苯醚型環氧樹脂中之市售品,例如可列舉:YSLV-80DE(新日鐵住金化學公司製造)等。 Examples of commercially available products among the above-mentioned diphenyl ether type epoxy resins include YSLV-80DE (manufactured by Nippon Steel & Sumikin Chemical Co., Ltd.).

作為上述二環戊二烯型環氧樹脂中之市售品,例如可列舉:EP-4088S(ADEKA公司製造)等。 As a commercial item among the said dicyclopentadiene-type epoxy resin, EP-4088S (made by ADEKA company) etc. are mentioned, for example.

作為上述萘型環氧樹脂中之市售品,例如可列舉:EPICLON HP 4032、EPICLON EXA-4700(均為DIC公司製造)等。 Examples of commercially available products among the above naphthalene-type epoxy resins include EPICLON HP 4032, EPICLON EXA-4700 (all manufactured by DIC Corporation), and the like.

作為上述苯酚酚醛清漆型環氧樹脂中之市售品,例如可列舉:EPICLON N-770(DIC公司製造)等。 As a commercial item among the said phenol novolak type epoxy resin, EPICLON N-770 (made by DIC Corporation) etc. are mentioned, for example.

作為上述鄰甲酚酚醛清漆型環氧樹脂中之市售品,例如可列舉:EPICLON N-670-EXP-S(DIC公司製造)等。 As a commercial item among the said ortho-cresol novolak type epoxy resin, EPICLON N-670-EXP-S (made by DIC Corporation) etc. are mentioned, for example.

作為上述二環戊二烯酚醛清漆型環氧樹脂中之市售品,例如可列舉:EPICLON HP 7200(DIC公司製造)等。 As a commercial item among the said dicyclopentadiene novolak type epoxy resin, EPICLON HP 7200 (made by DIC Corporation) etc. are mentioned, for example.

作為上述聯苯酚醛清漆型環氧樹脂中之市售品,例如可列舉:NC-3000P(日本化藥公司製造)等。 Examples of commercially available products among the above-mentioned biphenol novolak-type epoxy resins include NC-3000P (manufactured by Nippon Kayaku Co., Ltd.).

作為上述萘酚酚醛清漆型環氧樹脂中之市售品,例如可列舉:ESN-165S(新日鐵住金化學公司製造)等。 As a commercial item among the said naphthol novolak type epoxy resin, ESN-165S (made by Nippon Steel & Sumikin Chemical Co., Ltd.) etc. are mentioned, for example.

作為上述縮水甘油胺型環氧樹脂中之市售品,例如可列舉:jER630(三 菱化學公司製造)、EPICLON 430(DIC公司製造)、TETRAD-X(三菱瓦斯化學公司製造)等。 As a commercial product among the above-mentioned glycidylamine epoxy resins, for example, jER630 (three Ryo Chemical Company), EPICLON 430 (manufactured by DIC Company), TETRAD-X (manufactured by Mitsubishi Gas Chemical Company), etc.

作為上述烷基多元醇型環氧樹脂中之市售品,例如可列舉:ZX-1542(新日鐵住金化學公司製造)、EPICLON 726(DIC公司製造)、Epolight 80MFA(共榮社化學公司製造)、DENACOL EX-611(Nagase chemteX公司製造)等。 Examples of commercially available products among the alkyl polyol type epoxy resins include: ZX-1542 (manufactured by Nippon Steel & Sumikin Chemical Co., Ltd.), EPICLON 726 (manufactured by DIC Corporation), and Epolight 80MFA (manufactured by Kyoeisha Chemical Co., Ltd.) ), DENACOL EX-611 (manufactured by Nagase chemteX), etc.

作為上述橡膠改質型環氧樹脂中之市售品,例如可列舉:YR-450、YR-207(均為新日鐵住金化學公司製造)、Epolead PB(Daicel公司製造)等。 Examples of commercially available products among the above-mentioned rubber-modified epoxy resins include YR-450, YR-207 (all manufactured by Nippon Steel & Sumikin Chemical Co., Ltd.), Epolead PB (manufactured by Daicel), and the like.

作為上述縮水甘油酯化合物中之市售品,例如可列舉:DENACOL EX-147(Nagase chemteX公司製造)等。 Examples of commercially available products among the aforementioned glycidyl ester compounds include DENACOL EX-147 (manufactured by Nagase chemteX) and the like.

作為上述環氧化合物中之其他市售品,例如可列舉:YDC-1312、YSLV-80XY、YSLV-90CR(均為新日鐵住金化學公司製造)、XAC4151(旭化成公司製造)、jER1031、jER 1032(均為三菱化學公司製造)、EXA-7120(DIC公司製造)、TEPIC(日產化學公司製造)等。 As other commercially available products among the above epoxy compounds, for example, YDC-1312, YSLV-80XY, YSLV-90CR (all manufactured by Nippon Steel & Sumikin Chemical Co., Ltd.), XAC4151 (manufactured by Asahi Kasei Corporation), jER1031, jER 1032 (All manufactured by Mitsubishi Chemical Corporation), EXA-7120 (manufactured by DIC Corporation), TEPIC (manufactured by Nissan Chemical Corporation), etc.

作為上述環氧(甲基)丙烯酸酯中之市售品,例如可列舉:EBECRYL 860、EBECRYL 3200、EBECRYL 3201、EBECRYL 3412、EBECRYL 3600、EBECRYL 3700、EBECRYL 3701、EBECRYL 3702、EBECRYL 3703、EBECRYL 3800、EBECRYL 6040、EBECRYL RDX63182(均為Daicel-Allnex公司製造),EA-1010、EA-1020、EA-5323、EA-5520、EA-CHD、EMA-1020(均為新中村化學工業公司製造),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、Epoxy Ester 3000M、Epoxy Ester 3000A、Epoxy Ester 200EA、Epoxy Ester 400EA(均為共榮社化學公司製造),DENACOL Acrylate DA-141、DENACOL Acrylate DA-314、DENACOL Acrylate DA-911(均為Nagase chemteX公司製造)等。 Examples of commercially available products among the aforementioned epoxy (meth)acrylates include: EBECRYL 860, EBECRYL 3200, EBECRYL 3201, EBECRYL 3412, EBECRYL 3600, EBECRYL 3700, EBECRYL 3701, EBECRYL 3702, EBECRYL 3703, EBECRYL 3800, EBECRYL 6040, EBECRYL RDX63182 (all manufactured by Daicel-Allnex), EA-1010, EA-1020, EA-5323, EA-5520, EA-CHD, EMA-1020 (all manufactured by Shinnakamura Chemical Industry Co.), 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, Epoxy Ester 3000M, Epoxy Ester 3000A, Epoxy Ester 200EA, Epoxy Ester 400EA (all manufactured by Kyoeisha Chemical Co., Ltd.), DENACOL Acrylate DA-141, DENACOL Acrylate DA-314, DENACOL Acrylate DA-911 (all manufactured by Nagase chemteX), and the like.

又,作為上述環氧(甲基)丙烯酸酯,亦可較佳地使用部分(甲基)丙烯酸改質環氧樹脂。 In addition, as the epoxy (meth)acrylate, a partially (meth)acrylic modified epoxy resin can also be preferably used.

上述部分(甲基)丙烯酸改質環氧樹脂可藉由使2個以上之環氧化合物之一部分環氧基與(甲基)丙烯酸進行反應而獲得。 The above-mentioned partial (meth)acrylic modified epoxy resin can be obtained by reacting a partial epoxy group of two or more epoxy compounds with (meth)acrylic acid.

上述環氧(甲基)丙烯酸酯中,就可使所獲得之液晶顯示元件用密封劑成為接著性及硬化物之柔軟性兩者優異者之方面而言,較佳為含有「不具有芳香族骨架之脂肪族環氧(甲基)丙烯酸酯」。 Among the above-mentioned epoxy (meth)acrylates, it is preferable that the obtained sealant for liquid crystal display elements is excellent in both adhesiveness and flexibility of the cured product. The aliphatic epoxy (meth)acrylate of the skeleton".

作為上述脂肪族環氧(甲基)丙烯酸酯,較佳為藉由對脂肪族環氧化合物之環氧基進行(甲基)丙烯酸改質而獲得之脂肪族環氧(甲基)丙烯酸酯,更佳為1,6-己二醇二環氧(甲基)丙烯酸酯等烷基多元醇型環氧(甲基)丙烯酸酯。 The aliphatic epoxy (meth)acrylate is preferably an aliphatic epoxy (meth)acrylate obtained by modifying the epoxy group of an aliphatic epoxy compound with (meth)acrylic acid, More preferred is an alkyl polyol type epoxy (meth)acrylate such as 1,6-hexanediol diepoxy (meth)acrylate.

上述環氧(甲基)丙烯酸酯100重量份中之上述脂肪族環氧(甲基)丙烯酸酯之含量的較佳下限為1重量份,較佳上限為15重量份。藉由使上述脂肪族環氧(甲基)丙烯酸酯之含量在該範圍,所獲得之液晶顯示元件用密封劑成為兼顧接著性及硬化物之柔軟性之效果更優異者。上述脂肪族環氧(甲基)丙烯酸酯之含量的更佳下限為5重量份,更佳上限為12重量份。 The lower limit of the content of the aliphatic epoxy (meth)acrylate in 100 parts by weight of the epoxy (meth)acrylate is preferably 1 part by weight, and the upper limit is preferably 15 parts by weight. By setting the content of the aliphatic epoxy (meth)acrylate in this range, the obtained sealing compound for liquid crystal display elements is more excellent in the effect of achieving both adhesiveness and flexibility of the cured product. The lower limit of the content of the aliphatic epoxy (meth)acrylate is more preferably 5 parts by weight, and the upper limit is more preferably 12 parts by weight.

上述環氧(甲基)丙烯酸酯與上述環氧化合物之合計100重量份中之上述環氧(甲基)丙烯酸酯之含量超過50重量份且為90重量份以下。 若上述環氧(甲基)丙烯酸酯之含量為50重量份以下,則所獲得之液晶顯示元件用密封劑成為光硬化性或接著性較差者,或者會引起液晶污染。若上述環氧(甲基)丙烯酸酯之含量超過90重量份,則所獲得之液晶顯示元件用密封劑成為防透濕性或接著力較差者。上述環氧(甲基)丙烯酸酯之含量的較佳下限為60重量份,較佳上限為85重量份。 The content of the epoxy (meth)acrylate in a total of 100 parts by weight of the epoxy (meth)acrylate and the epoxy compound exceeds 50 parts by weight and is 90 parts by weight or less. If the content of the epoxy (meth)acrylate is 50 parts by weight or less, the obtained sealing compound for liquid crystal display elements will have poor photocurability or adhesiveness, or liquid crystal contamination will occur. If the content of the epoxy (meth)acrylate exceeds 90 parts by weight, the obtained sealing compound for liquid crystal display elements will have poor moisture permeability or adhesiveness. The preferable lower limit of the content of the epoxy (meth)acrylate is 60 parts by weight, and the preferable upper limit is 85 parts by weight.

再者,於含有上述部分(甲基)丙烯酸改質環氧樹脂之情形時,關於上述環氧(甲基)丙烯酸酯之含量,於將不具有環氧基之環氧(甲基)丙烯酸酯設為A,將上述部分(甲基)丙烯酸改質環氧樹脂設為B時,以下述式(I)表示。 Furthermore, in the case of containing the above-mentioned partial (meth)acrylic modified epoxy resin, regarding the content of the above-mentioned epoxy (meth)acrylate, the epoxy (meth)acrylate without epoxy group Let it be A, and let the said partial (meth)acrylic-modified epoxy resin be B, it is represented by following formula (I).

Figure 105132132-A0202-12-0008-1
Figure 105132132-A0202-12-0008-1

本發明之液晶顯示元件用密封劑除上述環氧(甲基)丙烯酸酯以外,亦可於不妨礙本發明之目的之範圍內含有其他(甲基)丙烯酸化合物。 The sealing compound for liquid crystal display elements of this invention may contain other (meth)acrylic compound in the range which does not interfere with the objective of this invention in addition to the said epoxy (meth)acrylate.

作為上述其他(甲基)丙烯酸系化合物,例如可列舉:藉由使具有羥基之化合物與(甲基)丙烯酸進行反應而獲得之(甲基)丙烯酸酯化合物、藉由使具有羥基之(甲基)丙烯酸衍生物與異氰酸酯化合物進行反應而獲得之(甲基)丙烯酸胺酯等。 As the above-mentioned other (meth)acrylic compounds, for example, a (meth)acrylate compound obtained by reacting a compound having a hydroxyl group with (meth)acrylic acid, and a (meth)acrylate compound having a hydroxyl group ) (Meth)acrylate amine ester obtained by reacting an acrylic acid derivative with an isocyanate compound.

作為上述(甲基)丙烯酸酯化合物中之單官能者,例如可列舉:(甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸丙酯、(甲基)丙烯酸正丁酯、(甲基)丙烯酸異丁酯、(甲基)丙烯酸第三丁酯、(甲基)丙烯酸2- 乙基己酯、(甲基)丙烯酸正辛酯、(甲基)丙烯酸異辛酯、(甲基)丙烯酸異壬酯、(甲基)丙烯酸異癸酯、(甲基)丙烯酸月桂酯、(甲基)丙烯酸異肉豆蔻酯、(甲基)丙烯酸硬脂酯、(甲基)丙烯酸2-羥基乙酯、(甲基)丙烯酸2-羥基丙酯、(甲基)丙烯酸2-羥基丁酯、(甲基)丙烯酸4-羥基丁酯、(甲基)丙烯酸環己酯、(甲基)丙烯酸異莰酯、(甲基)丙烯酸二環戊烯酯、(甲基)丙烯酸苄酯、(甲基)丙烯酸2-甲氧基乙酯、(甲基)丙烯酸2-乙氧基乙酯、(甲基)丙烯酸2-丁氧基乙酯、(甲基)丙烯酸2-苯氧基乙酯、甲氧基乙二醇(甲基)丙烯酸酯、甲氧基聚乙二醇(甲基)丙烯酸酯、苯氧基二乙二醇(甲基)丙烯酸酯、苯氧基聚乙二醇(甲基)丙烯酸酯、(甲基)丙烯酸四氫糠酯、乙基卡必醇(甲基)丙烯酸酯、(甲基)丙烯酸2,2,2-三氟乙酯、(甲基)丙烯酸2,2,3,3-四氟丙酯、(甲基)丙烯酸1H,1H,5H-八氟戊酯、醯亞胺(甲基)丙烯酸酯、(甲基)丙烯酸二甲胺基乙酯、(甲基)丙烯酸二乙胺基乙酯、琥珀酸2-(甲基)丙烯醯氧基乙酯、六氫鄰苯二甲酸2-(甲基)丙烯醯氧基乙酯、2-羥丙基鄰苯二甲酸2-(甲基)丙烯醯氧基乙酯、磷酸2-(甲基)丙烯醯氧基乙酯、(甲基)丙烯酸縮水甘油酯等。 Examples of monofunctional ones in the above-mentioned (meth)acrylate compounds include methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, and n-butyl (meth)acrylate. Esters, isobutyl (meth)acrylate, tert-butyl (meth)acrylate, 2-(meth)acrylate Ethylhexyl, n-octyl (meth)acrylate, isooctyl (meth)acrylate, isononyl (meth)acrylate, isodecyl (meth)acrylate, lauryl (meth)acrylate, ( Isomyristyl (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, dicyclopentenyl (meth)acrylate, benzyl (meth)acrylate, ( 2-Methoxyethyl (meth)acrylate, 2-ethoxyethyl (meth)acrylate, 2-butoxyethyl (meth)acrylate, 2-phenoxyethyl (meth)acrylate , Methoxyethylene glycol (meth)acrylate, Methoxypolyethylene glycol (meth)acrylate, Phenoxydiethylene glycol (meth)acrylate, Phenoxypolyethylene glycol ( Meth) acrylate, tetrahydrofurfuryl (meth)acrylate, ethyl carbitol (meth)acrylate, 2,2,2-trifluoroethyl (meth)acrylate, (meth)acrylic acid 2 ,2,3,3-Tetrafluoropropyl ester, (meth)acrylate 1H,1H,5H-octafluoropentyl ester, imine (meth)acrylate, dimethylaminoethyl (meth)acrylate, Diethylaminoethyl (meth)acrylate, 2-(meth)acryloxyethyl succinate, 2-(meth)acryloxyethyl hexahydrophthalate, 2-hydroxypropyl 2-(meth)acryloxyethyl phthalate, 2-(meth)acryloxyethyl phosphate, glycidyl (meth)acrylate, etc.

又,作為上述(甲基)丙烯酸酯化合物中之2官能者,例如可列舉:1,3-丁二醇二(甲基)丙烯酸酯、1,4-丁二醇二(甲基)丙烯酸酯、1,6-己二醇二(甲基)丙烯酸酯、1,9-壬二醇二(甲基)丙烯酸酯、1,10-癸二醇二(甲基)丙烯酸酯、乙二醇二(甲基)丙烯酸酯、二乙二醇二(甲基)丙烯酸酯、四乙二醇二(甲基)丙烯酸酯、聚乙二醇二(甲基)丙烯酸酯、2-正丁基-2-乙基-1,3-丙二醇二(甲基)丙烯酸酯、二丙二醇二(甲基)丙烯酸酯、三丙二醇二(甲基)丙烯酸酯、聚丙二醇二(甲基)丙烯酸酯、新戊二醇二(甲基)丙烯酸 酯、環氧乙烷加成雙酚A二(甲基)丙烯酸酯、環氧丙烷加成雙酚A二(甲基)丙烯酸酯、環氧乙烷加成雙酚F二(甲基)丙烯酸酯、二羥甲基二環戊二烯基二(甲基)丙烯酸酯、環氧乙烷改質異三聚氰酸二(甲基)丙烯酸酯、2-羥基-3-(甲基)丙烯醯氧基丙基(甲基)丙烯酸酯、碳酸酯二醇二(甲基)丙烯酸酯、聚醚二醇二(甲基)丙烯酸酯、聚酯二醇二(甲基)丙烯酸酯、聚己內酯二醇二(甲基)丙烯酸酯、聚丁二烯二醇二(甲基)丙烯酸酯等。 In addition, examples of the bifunctional ones in the above-mentioned (meth)acrylate compounds include 1,3-butanediol di(meth)acrylate and 1,4-butanediol di(meth)acrylate , 1,6-hexanediol di(meth)acrylate, 1,9-nonanediol di(meth)acrylate, 1,10-decanediol di(meth)acrylate, ethylene glycol two (Meth)acrylate, diethylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, polyethylene glycol di(meth)acrylate, 2-n-butyl-2 -Ethyl-1,3-propanediol di(meth)acrylate, dipropylene glycol di(meth)acrylate, tripropylene glycol di(meth)acrylate, polypropylene glycol di(meth)acrylate, neopentyl diacrylate Alcohol bis(meth)acrylic acid Ester, ethylene oxide addition of bisphenol A di(meth)acrylate, propylene oxide addition of bisphenol A di(meth)acrylate, ethylene oxide addition of bisphenol F di(meth)acrylic acid Esters, dimethylol dicyclopentadienyl di(meth)acrylate, ethylene oxide modified isocyanuric acid di(meth)acrylate, 2-hydroxy-3-(meth)propylene Acetoxypropyl (meth)acrylate, carbonate diol di(meth)acrylate, polyether diol di(meth)acrylate, polyester diol di(meth)acrylate, polyhexane Lactonediol di(meth)acrylate, polybutadienediol di(meth)acrylate, etc.

又,作為上述(甲基)丙烯酸酯化合物中之3官能以上者,例如可列舉:三羥甲基丙烷三(甲基)丙烯酸酯、環氧乙烷加成三羥甲基丙烷三(甲基)丙烯酸酯、環氧丙烷加成三羥甲基丙烷三(甲基)丙烯酸酯、己內酯改質三羥甲基丙烷三(甲基)丙烯酸酯、環氧乙烷加成異三聚氰酸三(甲基)丙烯酸酯、甘油三(甲基)丙烯酸酯、環氧丙烷加成甘油三(甲基)丙烯酸酯、新戊四醇三(甲基)丙烯酸酯、磷酸三(甲基)丙烯醯氧基乙酯、二-三羥甲基丙烷四(甲基)丙烯酸酯、新戊四醇四(甲基)丙烯酸酯、二新戊四醇五(甲基)丙烯酸酯、二新戊四醇六(甲基)丙烯酸酯等。 In addition, examples of the tri- or more functional (meth)acrylate compounds include trimethylolpropane tri(meth)acrylate, ethylene oxide addition trimethylolpropane tri(methyl) )Acrylate, propylene oxide addition trimethylolpropane tri(meth)acrylate, caprolactone modified trimethylolpropane tri(meth)acrylate, ethylene oxide addition isocyanuric acid Acid tri(meth)acrylate, glycerol tri(meth)acrylate, propylene oxide addition glycerol tri(meth)acrylate, neopentylerythritol tri(meth)acrylate, phosphoric acid tri(meth) Acrylic oxyethyl, di-trimethylolpropane tetra (meth) acrylate, neopentyl erythritol tetra (meth) acrylate, dineopentyl penta (meth) acrylate, dineopentyl Tetraol hexa(meth)acrylate etc.

作為上述藉由使具有羥基之(甲基)丙烯酸衍生物與異氰酸酯化合物進行反應而獲得之(甲基)丙烯酸胺酯,例如可藉由於觸媒量之錫系化合物存在下,使具有羥基之(甲基)丙烯酸衍生物2當量與具有2個異氰酸酯基之異氰酸酯化合物1當量進行反應而獲得。 As the aforementioned (meth)acrylic acid amine ester obtained by reacting a (meth)acrylic acid derivative having a hydroxyl group with an isocyanate compound, for example, a (meth)acrylate having a hydroxyl group can be made ( It is obtained by reacting 2 equivalents of a meth)acrylic acid derivative with 1 equivalent of an isocyanate compound having two isocyanate groups.

作為成為上述(甲基)丙烯酸胺酯之原料之異氰酸酯化合物,例如可列舉:異佛爾酮二異氰酸酯、2,4-甲苯二異氰酸酯、2,6-甲苯二異氰酸酯、六亞甲基二異氰酸酯、三甲基六亞甲基二異氰酸酯、二苯甲烷-4,4'-二異氰酸酯(MDI)、氫化MDI、聚合MDI、1,5-萘二異氰酸酯、 降莰烷二異氰酸酯、聯甲苯胺二異氰酸酯、苯二甲基二異氰酸酯(XDI)、氫化XDI、離胺酸二異氰酸酯、三苯甲烷三異氰酸酯、三(異氰酸酯基苯基)硫代磷酸酯、四甲基苯二甲基二異氰酸酯、1,6,11-十一烷三異氰酸酯等。 Examples of the isocyanate compound used as the raw material of the above (meth)acrylate amine ester include: isophorone diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, hexamethylene diisocyanate, Trimethylhexamethylene diisocyanate, diphenylmethane-4,4'-diisocyanate (MDI), hydrogenated MDI, polymeric MDI, 1,5-naphthalene diisocyanate, Norbornane diisocyanate, toluidine diisocyanate, xylylene diisocyanate (XDI), hydrogenated XDI, lysine diisocyanate, triphenylmethane triisocyanate, tris(isocyanatophenyl) phosphorothioate, four Methylxylylene diisocyanate, 1,6,11-undecane triisocyanate, etc.

又,作為成為上述(甲基)丙烯酸胺酯之原料之異氰酸酯化合物,例如亦可使用藉由乙二醇、丙二醇、甘油、山梨糖醇、三羥甲基丙烷、碳酸酯二醇、聚醚二醇、聚酯二醇、聚己內酯二醇等多元醇與過量之異氰酸酯化合物之反應而獲得之經鏈延長的異氰酸酯化合物。 In addition, as the isocyanate compound used as the raw material of the above-mentioned (meth)acrylate amine ester, for example, ethylene glycol, propylene glycol, glycerin, sorbitol, trimethylolpropane, carbonate diol, polyether two A chain-extended isocyanate compound obtained by the reaction of polyols such as alcohol, polyester diol, polycaprolactone diol and excess isocyanate compound.

作為成為上述(甲基)丙烯酸胺酯之原料之具有羥基之(甲基)丙烯酸衍生物,例如可列舉:(甲基)丙烯酸2-羥基乙酯、(甲基)丙烯酸2-羥基丙酯、(甲基)丙烯酸2-羥基丁酯、(甲基)丙烯酸4-羥基丁酯等(甲基)丙烯酸羥基烷基酯;或者乙二醇、丙二醇、1,3-丙二醇、1,3-丁二醇、1,4-丁二醇、聚乙二醇等二元醇之單(甲基)丙烯酸酯;或者三羥甲基乙烷、三羥甲基丙烷、甘油等三元醇之單(甲基)丙烯酸酯或二(甲基)丙烯酸酯;或者雙酚A型環氧丙烯酸酯等環氧(甲基)丙烯酸酯等。 Examples of the (meth)acrylic acid derivative having a hydroxyl group used as the raw material of the above-mentioned (meth)acrylate amine ester include: 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, Hydroxyalkyl (meth)acrylates such as 2-hydroxybutyl (meth)acrylate and 4-hydroxybutyl (meth)acrylate; or ethylene glycol, propylene glycol, 1,3-propanediol, 1,3-butane Mono(meth)acrylate of glycol, 1,4-butanediol, polyethylene glycol, etc.; or mono(meth)acrylate of triol such as trimethylolethane, trimethylolpropane, glycerin, etc. Meth)acrylate or di(meth)acrylate; or epoxy (meth)acrylate such as bisphenol A epoxy acrylate, etc.

作為上述(甲基)丙烯酸胺酯中之市售品,例如可列舉:M-1100、M-1200、M-1210、M-1600(均為東亞合成公司製造),EBECRYL 210、EBECRYL 220、EBECRYL 230、EBECRYL 270、EBECRYL 1290、EBECRYL 2220、EBECRYL 4827、EBECRYL 4842、EBECRYL 4858、EBECRYL 5129、EBECRYL 6700、EBECRYL 8402、EBECRYL 8803、EBECRYL 8804、EBECRYL 8807、EBECRYL 9260(均為Daicel-Allnex公司製造),Artresin UN-330、Artresin SH-500B、ArtresinUN-1200TPK、ArtresinUN-1255、ArtresinUN-3320HB、ArtresinUN-7100、ArtresinUN-9000A、ArtresinUN- 9000H(均為根上工業公司製造),U-2HA、U-2PHA、U-3HA、U-4HA、U-6H、U-6HA、U-6LPA、U-10H、U-15HA、U-108、U-108A、U-122A、U-122P、U-324A、U-340A、U-340P、U-1084A、U-2061BA、UA-340P、UA-4000、UA-4100、UA-4200、UA-4400、UA-5201P、UA-7100、UA-7200、UA-W2A(均為新中村化學工業公司製造),AH-600、AI-600、AT-600、UA-101I、UA-101T、UA-306H、UA-306I、UA-306T(均為共榮社化學公司製造)等。 Examples of commercially available products among the above (meth)acrylate amine esters include: M-1100, M-1200, M-1210, M-1600 (all manufactured by Toagosei Co., Ltd.), EBECRYL 210, EBECRYL 220, EBECRYL 230, EBECRYL 270, EBECRYL 1290, EBECRYL 2220, EBECRYL 4827, EBECRYL 4842, EBECRYL 4858, EBECRYL 5129, EBECRYL 6700, EBECRYL 8402, EBECRYL 8803, EBECRYL 8804, EBECRYL 8807, EBECRYL 9260 (all manufactured by EBECRYL 8807, EBECRYL 9260) Artresin UN-330, Artresin SH-500B, ArtresinUN-1200TPK, ArtresinUN-1255, ArtresinUN-3320HB, ArtresinUN-7100, ArtresinUN-9000A, ArtresinUN- 9000H (all manufactured by Nejo Industrial Co., Ltd.), U-2HA, U-2PHA, U-3HA, U-4HA, U-6H, U-6HA, U-6LPA, U-10H, U-15HA, U-108, U-108A, U-122A, U-122P, U-324A, U-340A, U-340P, U-1084A, U-2061BA, UA-340P, UA-4000, UA-4100, UA-4200, UA- 4400, UA-5201P, UA-7100, UA-7200, UA-W2A (all manufactured by Shinnakamura Chemical Industry Co., Ltd.), AH-600, AI-600, AT-600, UA-101I, UA-101T, UA- 306H, UA-306I, UA-306T (all manufactured by Kyoeisha Chemical Co., Ltd.), etc.

本發明之液晶顯示元件用密封劑含有1分子中具有1個以上之環氧基之環氧化合物。 The sealing compound for liquid crystal display elements of this invention contains the epoxy compound which has 1 or more epoxy groups in 1 molecule.

作為上述環氧化合物,例如可列舉與以上作為成為用以合成上述環氧(甲基)丙烯酸酯之原料之環氧化合物所述者相同者等。其中,就可使所獲得之液晶顯示元件用密封劑成為接著性及硬化物之柔軟性兩者優異者之方面而言,較佳為含有不具有芳香族骨架之脂肪族環氧化合物。 As said epoxy compound, the thing same as the thing mentioned above as the epoxy compound used as the raw material for synthesizing said epoxy (meth)acrylate etc. is mentioned, for example. Among them, it is preferable to contain an aliphatic epoxy compound that does not have an aromatic skeleton in terms of making the obtained sealing compound for liquid crystal display elements excellent in both the adhesiveness and the flexibility of the cured product.

再者,如上所述,部分(甲基)丙烯酸改質環氧樹脂係包含於上述環氧(甲基)丙烯酸酯中,而並不包含於上述環氧化合物中。 Furthermore, as described above, part of the (meth)acrylic modified epoxy resin is contained in the epoxy (meth)acrylate, but not in the epoxy compound.

本發明之液晶顯示元件用密封劑含有1分子中具有2個以上之順丁烯二醯亞胺基之多官能順丁烯二醯亞胺化合物。藉由含有上述多官能順丁烯二醯亞胺化合物,本發明之液晶顯示元件用密封劑成為防透濕性優異者。又,上述多官能順丁烯二醯亞胺化合物不僅可發揮作為硬化性樹脂之功能,亦可發揮作為聚合起始劑之功能。 The sealing compound for liquid crystal display elements of this invention contains the polyfunctional maleimide compound which has 2 or more maleimide groups in 1 molecule. By containing the said polyfunctional maleimide compound, the sealing compound for liquid crystal display elements of this invention becomes a thing excellent in moisture permeability. In addition, the above-mentioned polyfunctional maleimide compound not only functions as a curable resin, but also functions as a polymerization initiator.

作為上述多官能順丁烯二醯亞胺化合物,可較佳地使用下述式(1)所表示之化合物或下述式(2)所表示之化合物。 As the polyfunctional maleimide compound, a compound represented by the following formula (1) or a compound represented by the following formula (2) can be preferably used.

Figure 105132132-A0202-12-0013-2
Figure 105132132-A0202-12-0013-2

式(1)中,R1表示碳數2~3之伸烷基,n為2~40之整數。 In the formula (1), R 1 represents an alkylene group having 2 to 3 carbon atoms, and n is an integer of 2 to 40.

Figure 105132132-A0202-12-0013-3
Figure 105132132-A0202-12-0013-3

式(2)中,R2表示碳數1~45之2價脂肪族基。 In the formula (2), R 2 represents a divalent aliphatic group with 1 to 45 carbon atoms.

上述式(2)中,R2之碳數較佳為12~45。又,R2較佳為具有脂肪族環。 In the above formula (2), the carbon number of R 2 is preferably 12 to 45. Moreover, R 2 preferably has an aliphatic ring.

作為上述式(2)所表示之化合物,具體而言,例如可列舉:1,20-雙順丁烯二醯亞胺-10,11-二辛基-二十烷(下述式(3-1)所表示之化合物)、1-伸庚基順丁烯二醯亞胺-2-伸辛基順丁烯二醯亞胺-4-辛基-5-庚基環己烷(下述式(3-2)所表示之化合物)、1,2-二伸辛基順丁烯二醯亞胺-3-辛基-4-己基環己烷(下述式(3-3)所表示之化合物)等,可藉由美國專利第5973166號說明書中所記載之方法等而合成。 As the compound represented by the above formula (2), specifically, for example, 1,20-bismaleimide-10,11-dioctyl-eicosane (the following formula (3- 1) The compound represented), 1-heptylmaleimide-2-octylmaleimide-4-octyl-5-heptylcyclohexane (the following formula (3 -2) The compound represented by), 1,2-dioctylmaleimide-3-octyl-4-hexylcyclohexane (compound represented by the following formula (3-3)), etc., It can be synthesized by the method described in the specification of U.S. Patent No. 5,973,166.

Figure 105132132-A0202-12-0014-4
Figure 105132132-A0202-12-0014-4

Figure 105132132-A0202-12-0014-5
Figure 105132132-A0202-12-0014-5

Figure 105132132-A0202-12-0014-6
Figure 105132132-A0202-12-0014-6

上述環氧(甲基)丙烯酸酯與上述環氧化合物之合計100重量份中之上述多官能順丁烯二醯亞胺化合物的含量之較佳下限為0.1重量份,較佳上限為15重量份。藉由使上述多官能順丁烯二醯亞胺化合物之含量在該範圍,所獲得之液晶顯示元件用密封劑成為光硬化性、接著性、及防透濕性更優異者。上述多官能順丁烯二醯亞胺化合物之含量之更佳下限為1重量份,更佳上限為10重量份。 The lower limit of the content of the polyfunctional maleimide compound in the total 100 parts by weight of the epoxy (meth)acrylate and the epoxy compound is preferably 0.1 parts by weight, and the upper limit is preferably 15 parts by weight . By setting the content of the polyfunctional maleimide compound in this range, the obtained sealing compound for liquid crystal display elements is more excellent in photocurability, adhesiveness, and moisture permeability. The lower limit of the content of the polyfunctional maleimide compound is more preferably 1 part by weight, and the upper limit is more preferably 10 parts by weight.

如上所述,上述多官能順丁烯二醯亞胺化合物可發揮作為聚合起始劑之功能,但存在若僅憑上述多官能順丁烯二醯亞胺化合物則反應 性變得不充分之情況。因此,本發明之液晶顯示元件用密封劑較佳為含有聚合起始劑。 As described above, the above-mentioned polyfunctional maleimide compound can function as a polymerization initiator, but if the above-mentioned polyfunctional maleimide compound is present, it will react. A situation where sex becomes insufficient. Therefore, the sealing compound for liquid crystal display elements of this invention preferably contains a polymerization initiator.

作為上述聚合起始劑,可列舉:光自由基聚合起始劑或熱自由基聚合起始劑等,較佳為使用光自由基聚合起始劑。進而,就可使所獲得之液晶顯示元件用密封劑之接著性變得更好之方面而言,更佳為將光自由基聚合起始劑與熱自由基聚合起始劑或下述硬化促進劑併用。 As said polymerization initiator, a photo radical polymerization initiator, a thermal radical polymerization initiator, etc. are mentioned, It is preferable to use a photo radical polymerization initiator. Furthermore, in terms of improving the adhesiveness of the obtained sealing agent for liquid crystal display elements, it is more preferable to use a photo-radical polymerization initiator and a thermal radical polymerization initiator or the following hardening promotion Agent and use.

作為上述光自由基聚合起始劑,例如可列舉:二苯甲酮系化合物、苯乙酮系化合物、醯基氧化膦系化合物、二茂鈦系化合物、肟酯系化合物、安息香醚系化合物、9-氧硫

Figure 105132132-A0202-12-0015-11
(thioxanthone)等。其中,較佳為肟酯系化合物。 Examples of the aforementioned photoradical polymerization initiator include: benzophenone-based compounds, acetophenone-based compounds, phosphine oxide-based compounds, titanocene-based compounds, oxime ester-based compounds, benzoin ether-based compounds, 9-oxysulfur
Figure 105132132-A0202-12-0015-11
(thioxanthone) and so on. Among them, oxime ester compounds are preferred.

作為上述肟酯系化合物,例如可列舉:1-(4-(苯硫基)苯基)-1,2-辛二酮2-(O-苯甲醯基肟)、O-乙醯基-1-(6-(2-甲基苯甲醯基)-9-乙基-9H-咔唑-3-基)乙酮肟等。 Examples of the above-mentioned oxime ester-based compounds include: 1-(4-(phenylthio)phenyl)-1,2-octanedione 2-(O-benzyloxime), O-acetyl- 1-(6-(2-Methylbenzyl)-9-ethyl-9H-carbazol-3-yl)ethanone oxime and the like.

作為上述光自由基聚合起始劑中之市售品,例如可列舉:IRGACURE OXE01、IRGACURE OXE02、IRGACURE184、IRGACURE369、IRGACURE379、IRGACURE651、IRGACURE819、IRGACURE907、IRGACURE2959、Lucirin TPO(均為BASF公司製造),安息香甲醚、安息香乙醚、安息香丙醚(均為東京化成工業公司製造)等。 Examples of commercially available products among the above-mentioned photoradical polymerization initiators include: IRGACURE OXE01, IRGACURE OXE02, IRGACURE184, IRGACURE369, IRGACURE379, IRGACURE651, IRGACURE819, IRGACURE907, IRGACURE2959, Lucirin TPO (all manufactured by BASF), benzoin Methyl ether, benzoin ethyl ether, benzoin propyl ether (all manufactured by Tokyo Chemical Industry Co., Ltd.), etc.

關於上述光自由基聚合起始劑之含量,相對於上述環氧(甲基)丙烯酸酯與上述環氧化合物之合計100重量份,較佳之下限為0.1重量份,較佳之上限為10重量份。藉由使上述光自由基聚合起始劑之含量為該範圍,而可於不會使所獲得之液晶顯示元件用密封劑之保存穩定性等變差 之情況下使光硬化性變得更優異。上述光自由基聚合起始劑之含量之更佳下限為0.5重量份,更佳上限為5重量份。 Regarding the content of the photo-radical polymerization initiator, the lower limit is preferably 0.1 parts by weight, and the upper limit is preferably 10 parts by weight relative to 100 parts by weight of the total of the epoxy (meth)acrylate and the epoxy compound. By setting the content of the above-mentioned photo radical polymerization initiator within this range, the storage stability of the obtained sealing compound for liquid crystal display elements can not be deteriorated In this case, the photocurability becomes more excellent. The lower limit of the content of the above-mentioned photo radical polymerization initiator is more preferably 0.5 parts by weight, and the upper limit is more preferably 5 parts by weight.

作為上述熱自由基聚合起始劑,例如可列舉:由有機過氧化物、偶氮化合物等所構成者。其中,較佳為有機過氧化物。 Examples of the thermal radical polymerization initiator include those composed of organic peroxides, azo compounds, and the like. Among them, organic peroxides are preferred.

作為上述有機過氧化物,例如可列舉:過氧化二異丙苯、過氧化酮、過氧縮酮、過氧化氫、過氧化二烷基、過氧酯、過氧化二醯基、過氧化二碳酸酯等。其中,較佳為過氧化二異丙苯。 As the above-mentioned organic peroxides, for example, dicumyl peroxide, ketone peroxide, peroxyketal, hydrogen peroxide, dialkyl peroxide, peroxy ester, diacyl peroxide, dicumyl peroxide Carbonate etc. Among them, dicumyl peroxide is preferred.

作為上述偶氮化合物,較佳為由高分子偶氮化合物所構成之高分子偶氮起始劑。 The azo compound is preferably a polymer azo initiator composed of a polymer azo compound.

再者,於本說明書中,所謂高分子偶氮起始劑,意指具有偶氮基,且產生可藉由熱而使(甲基)丙烯醯氧基硬化之自由基之數量平均分子量為300以上的化合物。 Furthermore, in this specification, the so-called polymer azo initiator means that it has an azo group and generates a radical which can harden the (meth)acryloxy group by heat. The number average molecular weight is 300 The above compound.

上述高分子偶氮起始劑之數量平均分子量之較佳下限為1000,較佳上限為30萬。藉由使上述高分子偶氮起始劑之數量平均分子量為該範圍,可一面抑制液晶污染,一面容易地與硬化性樹脂混合。上述高分子偶氮起始劑之數量平均分子量之更佳下限為5000,更佳上限為10萬,進而較佳之下限為1萬,進而較佳之上限為9萬。 The preferred lower limit of the number average molecular weight of the polymer azo initiator is 1,000, and the preferred upper limit is 300,000. By setting the number average molecular weight of the polymer azo initiator to this range, it is possible to easily mix with the curable resin while suppressing liquid crystal contamination. The lower limit of the number average molecular weight of the polymer azo initiator is more preferably 5,000, the upper limit is more preferably 100,000, the lower limit is more preferably 10,000, and the upper limit is more preferably 90,000.

再者,於本說明書中,上述數量平均分子量係利用凝膠滲透層析法(GPC)進行測定,且根據聚苯乙烯換算而求出之值。作為利用GPC而對由聚苯乙烯換算所得之數量平均分子量進行測定時之管柱,例如可列舉:Shodex LF-804(昭和電工公司製造)等。 In addition, in this specification, the said number average molecular weight is the value calculated|required by the polystyrene conversion measured by gel permeation chromatography (GPC). As a column for measuring the number average molecular weight converted from polystyrene by GPC, for example, Shodex LF-804 (manufactured by Showa Denko Co., Ltd.) can be cited.

作為上述高分子偶氮起始劑,例如可列舉:具有經由偶氮基 鍵結有多個聚環氧烷或聚二甲基矽氧烷等單元而成之結構者。 Examples of the above-mentioned polymer azo initiator include: A structure formed by bonding multiple units such as polyalkylene oxide or polydimethylsiloxane.

作為具有上述經由偶氮基鍵結有多個聚環氧烷等單元而成之結構之高分子偶氮起始劑,較佳為具有聚環氧乙烷結構者。作為此種高分子偶氮起始劑,例如可列舉:4,4'-偶氮雙(4-氰基戊酸)與聚伸烷基二醇之縮聚物、或4,4'-偶氮雙(4-氰基戊酸)與具有末端胺基之聚二甲基矽氧烷之縮聚物等,具體而言,例如可列舉:VPE-0201、VPE-0401、VPE-0601、VPS-0501、VPS-1001(均為和光純藥工業公司製造)等。 As the polymer azo initiator having a structure in which a plurality of units such as polyalkylene oxide are bonded via an azo group, one having a polyethylene oxide structure is preferred. As such a polymer azo initiator, for example, a condensation polymer of 4,4'-azobis(4-cyanovaleric acid) and polyalkylene glycol, or 4,4'-azo The polycondensate of bis(4-cyanovaleric acid) and polydimethylsiloxane having a terminal amine group, etc., specifically, for example: VPE-0201, VPE-0401, VPE-0601, VPS-0501 , VPS-1001 (all manufactured by Wako Pure Chemical Industries, Ltd.), etc.

又,作為並非高分子之偶氮化合物之例,可列舉V-65、V-501(均為和光純藥工業公司製造)等。 In addition, examples of azo compounds that are not polymers include V-65 and V-501 (all manufactured by Wako Pure Chemical Industries, Ltd.).

關於上述熱自由基聚合起始劑之含量,相對於上述環氧(甲基)丙烯酸酯與上述環氧化合物之合計100重量份,較佳之下限為0.05重量份,較佳之上限為10重量份。藉由使上述熱自由基聚合起始劑之含量為該範圍,而可於不會使所獲得之液晶顯示元件用密封劑之保存穩定性等變差之情況下使熱硬化性變得更優異。上述熱自由基聚合起始劑之含量之更佳下限為0.1重量份,更佳上限為5重量份。 Regarding the content of the thermal radical polymerization initiator, the lower limit is preferably 0.05 parts by weight, and the upper limit is preferably 10 parts by weight relative to 100 parts by weight of the total of the epoxy (meth)acrylate and the epoxy compound. By setting the content of the thermal radical polymerization initiator within this range, it is possible to make the thermosetting properties more excellent without deteriorating the storage stability of the obtained sealing compound for liquid crystal display elements. . The lower limit of the content of the thermal radical polymerization initiator is more preferably 0.1 parts by weight, and the upper limit is more preferably 5 parts by weight.

本發明之液晶顯示元件用密封劑亦可含有熱硬化劑。 The sealing compound for liquid crystal display elements of this invention may contain a thermosetting agent.

作為上述熱硬化劑,例如可列舉:有機酸醯肼、咪唑衍生物、胺化合物、多酚系化合物、酸酐等。其中,可較佳地使用固體之有機酸醯肼。 As said thermosetting agent, organic acid hydrazine, imidazole derivatives, amine compounds, polyphenol compounds, acid anhydrides, etc. are mentioned, for example. Among them, solid organic acid hydrazine can be preferably used.

作為上述固體之有機酸醯肼,例如可列舉:1,3-雙(肼基碳乙基-5-異丙基乙內醯脲)、癸二酸二醯肼、間苯二甲酸二醯肼、己二酸二醯肼、丙二酸二醯肼等,作為市售品,例如可列舉:SDH、ADH(大塚化學公司製造)、MDH(Japan Finechem公司製造)、Amicure VDH、Amicure VDH -J、Amicure UDH(均為Ajinomoto Fine-Techno公司製造)等。 Examples of the above-mentioned solid organic acid hydrazine include: 1,3-bis(hydrazinocarbethyl-5-isopropylhydantoin), dihydrazide sebacate, and dihydrazide isophthalate , Dihydrazine adipic acid, Dihydrazine malonate, etc., as commercially available products, for example, SDH, ADH (manufactured by Otsuka Chemical Co., Ltd.), MDH (manufactured by Japan Finechem Co., Ltd.), Amicure VDH, Amicure VDH -J, Amicure UDH (all manufactured by Ajinomoto Fine-Techno), etc.

關於上述熱硬化劑之含量,相對於上述環氧(甲基)丙烯酸酯與上述環氧化合物之合計100重量份,較佳之下限為1重量份,較佳之上限為50重量份。藉由使上述熱硬化劑之含量為該範圍,而可於不會使所獲得之液晶顯示元件用密封劑之塗佈性等變差之情況下使熱硬化性變得更優異。上述熱硬化劑之含量之更佳上限為30重量份。 Regarding the content of the thermosetting agent, the lower limit is preferably 1 part by weight, and the upper limit is preferably 50 parts by weight relative to the total of 100 parts by weight of the epoxy (meth)acrylate and the epoxy compound. By making the content of the said thermosetting agent into this range, the thermosetting property can be made more excellent without deteriorating the coatability etc. of the sealing compound for liquid crystal display elements obtained. The more preferable upper limit of the content of the thermal hardening agent is 30 parts by weight.

作為上述硬化促進劑,可列舉:胺加成化合物、三級胺類、膦類等。其中,較佳為胺加成化合物。 As said hardening accelerator, amine addition compounds, tertiary amines, phosphines, etc. are mentioned. Among them, amine addition compounds are preferred.

關於上述硬化促進劑之含量,相對於上述環氧(甲基)丙烯酸酯與上述環氧化合物之合計100重量份,較佳之下限為0.5重量份,較佳之上限為40重量份。藉由使上述硬化促進劑之含量為該範圍,而可於不會使所獲得之液晶顯示元件用密封劑之保存穩定性等變差之情況下使硬化性變得更優異。 Regarding the content of the curing accelerator, the lower limit is preferably 0.5 parts by weight, and the upper limit is preferably 40 parts by weight relative to 100 parts by weight of the total of the epoxy (meth)acrylate and the epoxy compound. By making the content of the said hardening accelerator into this range, the hardening property can be made more excellent without deteriorating the storage stability etc. of the sealing compound for liquid crystal display elements obtained.

本發明之液晶顯示元件用密封劑就進一步提高所獲得之液晶顯示元件用密封劑之硬化物之柔軟性或接著性等之觀點而言,較佳為含有柔軟粒子。 The sealing compound for liquid crystal display elements of the present invention preferably contains soft particles from the viewpoint of further improving the flexibility or adhesiveness of the cured product of the obtained sealing compound for liquid crystal display elements.

作為上述柔軟粒子,例如可列舉:聚矽氧系粒子、乙烯系粒子、胺酯(urethane)系粒子、氟系粒子、腈系粒子等。其中,較佳為聚矽氧系粒子、乙烯系粒子。 Examples of the above-mentioned flexible particles include silicone-based particles, ethylene-based particles, urethane-based particles, fluorine-based particles, and nitrile-based particles. Among them, polysiloxane-based particles and ethylene-based particles are preferred.

作為上述聚矽氧系粒子,就於樹脂中之分散性之觀點而言,較佳為聚矽氧橡膠粒子。 As the aforementioned silicone-based particles, silicone rubber particles are preferred from the viewpoint of dispersibility in the resin.

作為上述乙烯系粒子,可較佳地使用(甲基)丙烯酸粒子。 As the aforementioned vinyl particles, (meth)acrylic particles can be preferably used.

上述(甲基)丙烯酸粒子可藉由利用公知之方法使成為原料之單體進行聚合而獲得。具體而言,例如可列舉:於自由基聚合起始劑之存在下使單體進行懸浮聚合之方法、藉由於自由基聚合起始劑之存在下使非交聯之種子粒子吸收單體而使種子粒子膨潤從而進行種子聚合之方法等。 The (meth)acrylic particles can be obtained by polymerizing monomers used as raw materials by a known method. Specifically, for example, a method of suspension polymerization of monomers in the presence of a radical polymerization initiator, and a method of absorbing monomers by non-crosslinked seed particles in the presence of a radical polymerization initiator Seed particles swell to carry out seed polymerization methods, etc.

作為成為用以形成上述(甲基)丙烯酸粒子之原料之單體,例如可列舉:(甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸丙酯、(甲基)丙烯酸丁酯、(甲基)丙烯酸己酯、(甲基)丙烯酸辛酯、(甲基)丙烯酸2-乙基己酯、(甲基)丙烯酸月桂酯、(甲基)丙烯酸鯨蠟酯、(甲基)丙烯酸硬脂酯、(甲基)丙烯酸環己酯、(甲基)丙烯酸異莰酯等(甲基)丙烯酸烷基酯類;或(甲基)丙烯酸2-羥基乙酯、甘油(甲基)丙烯酸酯、聚氧乙烯(甲基)丙烯酸酯、(甲基)丙烯酸縮水甘油酯等含氧原子之(甲基)丙烯酸酯類;或(甲基)丙烯腈等含腈單體;或(甲基)丙烯酸三氟甲酯,(甲基)丙烯酸五氟乙酯等含氟之(甲基)丙烯酸酯類等單官能單體。其中,就均聚物之Tg較低,且可使施加有1g負載時之變形量變大之方面而言,較佳為(甲基)丙烯酸烷基酯類。 Examples of monomers used as the raw materials for forming the (meth)acrylic particles include: methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, and (meth)acrylate. Butyl acrylate, hexyl (meth)acrylate, octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, lauryl (meth)acrylate, cetyl (meth)acrylate, ( Stearyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate and other alkyl (meth)acrylates; or 2-hydroxyethyl (meth)acrylate, glycerin ( Oxygen-containing (meth)acrylates such as meth)acrylate, polyoxyethylene (meth)acrylate, and glycidyl (meth)acrylate; or nitrile-containing monomers such as (meth)acrylonitrile; Or trifluoromethyl (meth)acrylate, pentafluoroethyl (meth)acrylate and other fluorine-containing (meth)acrylates and other monofunctional monomers. Among them, the homopolymer has a low Tg and can increase the amount of deformation when a load of 1 g is applied, and alkyl (meth)acrylates are preferred.

又,為了具有交聯結構,可使用四羥甲基甲烷四(甲基)丙烯酸酯、四羥甲基甲烷三(甲基)丙烯酸酯、四羥甲基甲烷二(甲基)丙烯酸酯、三羥甲基丙烷三(甲基)丙烯酸酯、二新戊四醇六(甲基)丙烯酸酯、二新戊四醇五(甲基)丙烯酸酯、甘油三(甲基)丙烯酸酯、甘油二(甲基)丙烯酸酯、(聚)乙二醇二(甲基)丙烯酸酯、(聚)丙二醇二(甲基)丙烯酸酯、(聚)四亞甲基二(甲基)丙烯酸酯、1,4-丁二醇二(甲基)丙烯酸酯、1,6-己二醇二(甲基)丙烯酸酯、異三聚氰酸骨架三(甲基)丙烯酸酯等多官能單體。其中,就交聯點間之分子量較大,且可使施加1g負載時之變形量變大之方面而言,較佳為(聚) 乙二醇二(甲基)丙烯酸酯、(聚)丙二醇二(甲基)丙烯酸酯、(聚)四亞甲基二(甲基)丙烯酸酯、1,4-丁二醇二(甲基)丙烯酸酯、1,6-己二醇二(甲基)丙烯酸酯。 In addition, in order to have a crosslinked structure, tetramethylolmethane tetra(meth)acrylate, tetramethylolmethane tri(meth)acrylate, tetramethylolmethane di(meth)acrylate, trimethylolmethane can be used. Hydroxymethylpropane tri(meth)acrylate, dineopentaerythritol hexa(meth)acrylate, dineopentaerythritol penta(meth)acrylate, glycerol tri(meth)acrylate, glycerol di(meth)acrylate Meth) acrylate, (poly)ethylene glycol di(meth)acrylate, (poly)propylene glycol di(meth)acrylate, (poly)tetramethylene di(meth)acrylate, 1,4 -Multifunctional monomers such as butanediol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, and isocyanuric acid skeleton tri(meth)acrylate. Among them, in terms of the molecular weight between the cross-linking points is relatively large and the deformation amount when a load of 1 g is applied can be increased, (poly) Ethylene glycol di(meth)acrylate, (poly)propylene glycol di(meth)acrylate, (poly)tetramethylene di(meth)acrylate, 1,4-butanediol di(meth) Acrylate, 1,6-hexanediol di(meth)acrylate.

關於上述交聯性單體之使用量,於成為用以形成上述(甲基)丙烯酸粒子之原料之單體整體中,較佳之下限為1重量%,較佳之上限為90重量%。藉由使上述交聯性單體之使用量為1重量%以上,而耐溶劑性提高,而於與各種密封劑原料混練時不會引起膨潤等問題,從而易於均勻地分散。藉由使上述交聯性單體之使用量為90重量%以下,可降低恢復率。上述交聯性單體之使用量之更佳之下限為3重量%,更佳之上限為80重量%。 Regarding the amount of the crosslinkable monomer used, in the entire monomer used as the raw material for forming the (meth)acrylic particles, the lower limit is preferably 1% by weight, and the upper limit is preferably 90% by weight. By making the use amount of the above-mentioned cross-linkable monomer 1% by weight or more, the solvent resistance is improved, and it does not cause problems such as swelling when kneading with various sealant materials, and it is easy to uniformly disperse. By making the usage amount of the above-mentioned crosslinkable monomer 90% by weight or less, the recovery rate can be reduced. The lower limit of the amount of the crosslinkable monomer used is more preferably 3% by weight, and the upper limit is more preferably 80% by weight.

進而,除該等丙烯酸系之單體以外,亦可使用苯乙烯、α-甲基苯乙烯等苯乙烯系單體;或甲基乙烯醚、乙基乙烯醚、丙基乙烯醚等乙烯醚類;或乙酸乙烯酯、丁酸乙烯酯、月桂酸乙烯酯、硬脂酸乙烯酯等羧酸乙烯酯類;或乙烯、丙烯、異戊二烯、丁二烯等不飽和烴;或氯乙烯、氟乙烯、氯苯乙烯等含鹵素之單體;或(異)氰尿酸三烯丙酯、偏苯三酸三烯丙酯(triallyl trimellitate)、二乙烯苯、鄰苯二甲酸二烯丙酯、二烯丙基丙烯醯胺、二烯丙醚、γ-(甲基)丙烯醯氧基丙基三甲氧基矽烷、三甲氧基矽基苯乙烯、乙烯基三甲氧基矽烷等單體。 Furthermore, in addition to these acrylic monomers, styrene monomers such as styrene and α-methylstyrene; or vinyl ethers such as methyl vinyl ether, ethyl vinyl ether, and propyl vinyl ether can also be used. ; Or vinyl acetate, vinyl butyrate, vinyl laurate, vinyl stearate and other vinyl carboxylates; or unsaturated hydrocarbons such as ethylene, propylene, isoprene, butadiene; or vinyl chloride, Halogen-containing monomers such as vinyl fluoride and chlorostyrene; or (iso) triallyl cyanurate, triallyl trimellitate, divinylbenzene, diallyl phthalate, Monomers such as diallyl acrylamide, diallyl ether, γ-(meth)acryloxy propyl trimethoxysilane, trimethoxysilylstyrene, vinyl trimethoxysilane, etc.

作為上述(甲基)丙烯酸系粒子,亦可較佳地使用核殼(甲基)丙烯酸酯共聚物微粒子。 As the aforementioned (meth)acrylic particles, core-shell (meth)acrylate copolymer fine particles can also be preferably used.

作為上述核殼(甲基)丙烯酸酯共聚物微粒子中之市售品,例如可列舉:F351(瑞翁化成公司製造)等。 Examples of commercially available products among the core-shell (meth)acrylate copolymer microparticles include F351 (manufactured by Zeon Chemical Co., Ltd.).

又,作為上述乙烯系粒子,例如亦可使用聚二乙烯苯粒子、聚氯丁二烯粒子、丁二烯橡膠粒子等。 In addition, as the above-mentioned ethylene-based particles, for example, polyvinylidenebenzene particles, polychloroprene particles, butadiene rubber particles, and the like can also be used.

上述柔軟粒子之平均粒徑之較佳下限為0.01μm,較佳之上限為10μm。藉由使上述柔軟粒子之平均粒徑為該範圍,而使提高所獲得之液晶顯示元件用密封劑之硬化物之柔軟性或接著性之效果變得更優異。上述柔軟粒子之平均粒徑之更佳下限為0.1μm,更佳上限為8μm。 The preferred lower limit of the average particle diameter of the soft particles is 0.01 μm, and the preferred upper limit is 10 μm. By making the average particle diameter of the said flexible particle into this range, the effect of improving the flexibility or adhesiveness of the cured product of the sealing compound for liquid crystal display elements obtained becomes more excellent. The lower limit of the average particle diameter of the soft particles is more preferably 0.1 μm, and the upper limit is more preferably 8 μm.

再者,於本說明書中,上述柔軟粒子之平均粒徑意指使用雷射繞射式粒度分佈測定裝置對摻合於密封劑之前之粒子進行測定而獲得之值。作為上述雷射繞射式分佈測定裝置,可使用Mastersizer-2000(Malvern公司製造)等。 Furthermore, in this specification, the average particle size of the soft particles mentioned above means the value obtained by measuring the particles before blending in the sealant using a laser diffraction particle size distribution measuring device. As the above-mentioned laser diffraction type distribution measuring device, Mastersizer-2000 (manufactured by Malvern Corporation) or the like can be used.

上述柔軟粒子之硬度之較佳下限為10,較佳上限為50。藉由使上述柔軟粒子之硬度為該範圍,而使提高所獲得之液晶顯示元件用密封劑之硬化物之柔軟性或接著性之效果變得更優異。上述柔軟粒子之硬度之更佳下限為20,更佳上限為40。 The preferred lower limit of the hardness of the soft particles is 10, and the preferred upper limit is 50. By making the hardness of the said soft particle into this range, the effect of improving the flexibility or adhesiveness of the cured product of the sealing compound for liquid crystal display elements obtained becomes more excellent. The lower limit of the hardness of the soft particles is more preferably 20, and the upper limit is more preferably 40.

再者,於本說明書中,上述柔軟粒子之硬度意指藉由依據JIS K 6253之方法而測定之硬度計A硬度。 In addition, in this specification, the hardness of the soft particles mentioned above means the hardness of durometer A measured by a method based on JIS K 6253.

本發明之液晶顯示元件用密封劑100重量份中之上述柔軟粒子之含量之較佳下限為5重量份,較佳上限為50重量份。藉由使上述柔軟粒子之含量為該範圍,而使提高所獲得之液晶顯示元件用密封劑之硬化物之柔軟性或接著性之效果變得更優異。上述柔軟粒子之含量之更佳下限為10重量份,更佳上限為30重量份。 The lower limit of the content of the soft particles in 100 parts by weight of the sealing compound for liquid crystal display elements of the present invention is preferably 5 parts by weight, and the upper limit is preferably 50 parts by weight. By setting the content of the soft particles in this range, the effect of improving the flexibility or adhesiveness of the cured product of the obtained sealing compound for liquid crystal display elements becomes more excellent. The lower limit of the content of the soft particles is more preferably 10 parts by weight, and the upper limit is more preferably 30 parts by weight.

關於本發明之液晶顯示元件用密封劑,為了提高黏度、進一 步提高基於應力分散效果之接著性、及改善線膨脹率等,較佳為含有填充劑。 Regarding the sealing compound for liquid crystal display elements of the present invention, in order to increase the viscosity, further In order to improve the adhesiveness based on the stress dispersion effect, and improve the linear expansion rate, it is preferable to contain a filler.

作為上述填充劑,例如可列舉:二氧化矽、滑石、玻璃珠、石棉、石膏、矽藻土、膨潤石、膨土、蒙脫石、絹雲母、活性白土、氧化鋁、氧化鋅、氧化鐵、氧化鎂、氧化錫、氧化鈦、碳酸鈣、碳酸鎂、氫氧化鎂、氫氧化鋁、氮化鋁、氮化矽、硫酸鋇、矽酸鈣等無機填充劑、或上述柔軟粒子所包含之除此以外之有機填充劑。 Examples of the above-mentioned fillers include: silica, talc, glass beads, asbestos, gypsum, diatomaceous earth, bentonite, bentonite, montmorillonite, sericite, activated clay, alumina, zinc oxide, iron oxide , Magnesium oxide, tin oxide, titanium oxide, calcium carbonate, magnesium carbonate, magnesium hydroxide, aluminum hydroxide, aluminum nitride, silicon nitride, barium sulfate, calcium silicate and other inorganic fillers, or included in the above soft particles Other organic fillers.

本發明之液晶顯示元件用密封劑100重量份中,上述填充劑之含量的較佳下限為10重量份,較佳上限為70重量份。藉由使上述填充劑之含量為該範圍,而於不會使塗佈性等變差之情況下使提高接著性等效果變得更優異。上述填充劑之含量之更佳下限為20重量份,更佳上限為60重量份。 In 100 parts by weight of the sealing compound for liquid crystal display elements of the present invention, the lower limit of the content of the filler is preferably 10 parts by weight, and the upper limit is preferably 70 parts by weight. By setting the content of the filler in this range, the effect of improving adhesiveness and the like becomes more excellent without deteriorating coatability and the like. The lower limit of the filler content is more preferably 20 parts by weight, and the upper limit is more preferably 60 parts by weight.

本發明之液晶顯示元件用密封劑較佳為含有矽烷偶合劑。上述矽烷偶合劑主要具有作為用以將密封劑與基板等更好地接著之接著助劑之功能。 It is preferable that the sealing compound for liquid crystal display elements of this invention contains a silane coupling agent. The above-mentioned silane coupling agent mainly functions as an adhesive auxiliary agent for better bonding the sealant and the substrate.

作為上述矽烷偶合劑,就提高與基板等之接著性之效果優異,且可藉由與硬化性樹脂進行化學鍵結而抑制硬化性樹脂向液晶中流出之方面而言,例如可較佳地使用3-胺基丙基三甲氧基矽烷、3-巰丙基三甲氧基矽烷、3-縮水甘油氧基丙基三甲氧基矽烷、3-異氰酸酯基丙基三甲氧基矽烷等。 As the above-mentioned silane coupling agent, it is excellent in the effect of improving the adhesion with the substrate, etc., and can inhibit the outflow of the curable resin into the liquid crystal by chemical bonding with the curable resin, for example, 3 -Aminopropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-isocyanatopropyltrimethoxysilane, etc.

本發明之液晶顯示元件用密封劑100重量份中,上述矽烷偶合劑之含量的較佳下限為0.1重量份,較佳上限為10重量份。藉由使上述 矽烷偶合劑之含量為該範圍,而一面抑制液晶污染之發生,一面使提高接著性之效果變得更優異。上述矽烷偶合劑之含量之更佳下限為0.3重量份,更佳上限為5重量份。 In 100 parts by weight of the sealing compound for liquid crystal display elements of the present invention, the lower limit of the content of the silane coupling agent is preferably 0.1 parts by weight, and the upper limit is preferably 10 parts by weight. By making the above The content of the silane coupling agent is within this range, and while suppressing the occurrence of liquid crystal contamination, the effect of improving adhesion becomes more excellent. The lower limit of the content of the silane coupling agent is more preferably 0.3 parts by weight, and the upper limit is more preferably 5 parts by weight.

本發明之液晶顯示元件用密封劑亦可含有遮光劑。藉由含有上述遮光劑,本發明之液晶顯示元件用密封劑可較佳地用作遮光密封劑。 The sealing compound for liquid crystal display elements of this invention may contain a light-shielding agent. By containing the said light-shielding agent, the sealing compound for liquid crystal display elements of this invention can be used suitably as a light-shielding sealing compound.

作為上述遮光劑,例如可列舉:鈦黑、苯胺黑、花青黑(cyanine black)、富勒烯、碳黑、樹脂被覆型碳黑等。又,作為上述無機填充劑而列舉之氧化鐵或氧化鈦等亦可用作上述遮光劑。其中,較佳為鈦黑。 As said light-shielding agent, titanium black, aniline black, cyanine black, fullerene, carbon black, resin-coated carbon black, etc. are mentioned, for example. Moreover, iron oxide, titanium oxide, etc. mentioned as the said inorganic filler can also be used as the said light-shielding agent. Among them, titanium black is preferred.

上述鈦黑係與對波長300~800nm之光之平均透光率相比,對紫外線區域附近、尤其是波長370~450nm之光之透光率更高之物質。即,上述鈦黑係具有如下性質的遮光劑,即藉由將可見光區域之波長之光充分地遮蔽而對本發明之液晶顯示元件用密封劑賦予遮光性,另一方面使紫外線區域附近之波長之光透過。作為本發明之液晶顯示元件用密封劑所含有之遮光劑,較佳為絕緣性較高之物質,作為絕緣性較高之遮光劑,鈦黑亦較佳。 The above-mentioned titanium black is a substance with a higher light transmittance in the vicinity of the ultraviolet region, especially light with a wavelength of 370 to 450 nm, compared to the average transmittance of light with a wavelength of 300 to 800 nm. That is, the above-mentioned titanium black is a light-shielding agent having a property of imparting light-shielding properties to the sealing compound for liquid crystal display elements of the present invention by sufficiently shielding light of wavelengths in the visible light region, and on the other hand, making the wavelength near the ultraviolet region Light through. As the light-shielding agent contained in the sealing compound for liquid crystal display elements of the present invention, a substance with high insulation is preferable, and as a light-shielding agent with high insulation, titanium black is also preferable.

上述鈦黑即便為未經表面處理者,亦發揮充分之效果,但亦可使用表面經偶合劑等有機成分處理者、或表面經氧化矽、氧化鈦、氧化鍺、氧化鋁、氧化鋯、氧化鎂等無機成分被覆者等,即使用經表面處理之鈦黑。其中,就可進一步提高絕緣性之方面而言,較佳為經有機成分處理者。 The above-mentioned titanium black exhibits sufficient effects even if it is not surface-treated, but it can also be used with the surface treated with organic components such as coupling agent, or the surface with silicon oxide, titanium oxide, germanium oxide, aluminum oxide, zirconium oxide, or oxide. For those coated with inorganic components such as magnesium, use surface-treated titanium black. Among them, in terms of further improving insulation properties, those treated with organic components are preferred.

又,使用含有上述鈦黑作為遮光劑之本發明之液晶顯示元件用密封劑而製造的液晶顯示元件由於具有充分之遮光性,故而可實現無漏光、具有 較高之對比度且具有優異之圖像顯示品質之液晶顯示元件。 In addition, the liquid crystal display element manufactured using the sealing compound for liquid crystal display element of the present invention containing the titanium black as a light-shielding agent has sufficient light-shielding properties, and therefore can achieve no light leakage and have A liquid crystal display element with high contrast and excellent image display quality.

作為上述鈦黑中之市售品,例如可列舉:12S、13M、13M-C、13R-N、14M-C(均為Mitsubishi Materials公司製造)、Tilack D(Ako Kasei公司製造)等。 Examples of commercially available products among the aforementioned titanium blacks include 12S, 13M, 13M-C, 13R-N, 14M-C (all manufactured by Mitsubishi Materials), Tilack D (manufactured by Ako Kasei), and the like.

上述鈦黑之比表面積之較佳下限為13m2/g,較佳上限為30m2/g,更佳之下限為15m2/g,更佳之上限為25m2/g。 The preferred lower limit of the specific surface area of the titanium black is 13 m 2 /g, the preferred upper limit is 30 m 2 /g, the more preferred lower limit is 15 m 2 /g, and the more preferred upper limit is 25 m 2 /g.

又,上述鈦黑之體積電阻之較佳下限為0.5Ω‧cm,較佳上限為3Ω‧cm,更佳之下限為1Ω‧cm,更佳之上限為2.5Ω‧cm。 In addition, the preferred lower limit of the volume resistance of the titanium black is 0.5Ω‧cm, the preferred upper limit is 3Ω‧cm, the more preferred lower limit is 1Ω‧cm, and the more preferred upper limit is 2.5Ω‧cm.

上述遮光劑之一次粒徑只要為液晶顯示元件之基板間之距離以下,則並無特別限定,較佳之下限為1nm,較佳之上限為5000nm。藉由使上述遮光劑之一次粒徑為該範圍,而可於不會使所獲得之液晶顯示元件用密封劑之塗佈性等變差之情況下使遮光性變得更優異。上述遮光劑之一次粒徑之更佳下限為5nm,更佳上限為200nm,進而較佳之下限為10nm,進而較佳之上限為100nm。 The primary particle size of the aforementioned light-shielding agent is not particularly limited as long as it is less than the distance between the substrates of the liquid crystal display element, and the preferred lower limit is 1 nm, and the preferred upper limit is 5000 nm. By making the primary particle diameter of the said light-shielding agent into this range, the light-shielding property can be made more excellent without deteriorating the coatability etc. of the sealing compound for liquid crystal display elements obtained. The lower limit of the primary particle size of the sunscreen is more preferably 5 nm, the upper limit is more preferably 200 nm, the lower limit is still more preferably 10 nm, and the upper limit is more preferably 100 nm.

再者,上述遮光劑之一次粒徑可使用NICOMP 380ZLS(PARTICLE SIZING SYSTEMS公司製造),使上述遮光劑分散於溶劑(水、有機溶劑等)而進行測定。 In addition, the primary particle size of the sunscreen can be measured by dispersing the sunscreen in a solvent (water, organic solvent, etc.) using NICOMP 380ZLS (manufactured by PARTICLE SIZING SYSTEMS).

本發明之液晶顯示元件用密封劑100重量份中,上述遮光劑之含量的較佳下限為5重量份,較佳上限為80重量份。藉由使上述遮光劑之含量為該範圍,而可於不會降低所獲得之液晶顯示元件用密封劑對基板之密合性、硬化後之強度或繪圖性之情況下發揮更優異之遮光性。上述遮光劑之含量之更佳下限為10重量份,更佳上限為70重量份,進而較佳之下 限為30重量份,進而較佳之上限為60重量份。 In 100 parts by weight of the sealing compound for liquid crystal display elements of the present invention, the lower limit of the content of the light-shielding agent is preferably 5 parts by weight, and the upper limit is preferably 80 parts by weight. By setting the content of the above-mentioned light-shielding agent in this range, it is possible to exhibit more excellent light-shielding properties without reducing the adhesion of the obtained liquid crystal display element sealant to the substrate, the strength after curing, or the drawing properties . The lower limit of the content of the sunscreen is more preferably 10 parts by weight, the upper limit is more preferably 70 parts by weight, and even more preferably less than The upper limit is 30 parts by weight, and the more preferable upper limit is 60 parts by weight.

本發明之液晶顯示元件用密封劑亦可進而視需要含有反應性稀釋劑、觸變劑、間隔物、硬化促進劑、消泡劑、整平劑、聚合抑制劑等添加劑。 The sealing compound for liquid crystal display elements of the present invention may further contain additives such as a reactive diluent, a thixotropic agent, a spacer, a hardening accelerator, a defoamer, a leveling agent, and a polymerization inhibitor as necessary.

作為製造本發明之液晶顯示元件用密封劑之方法,例如可列舉:使用勻相分散機、均質攪拌機、萬能攪拌機、行星式混合機、捏合機、三輥研磨機等混合機,將環氧(甲基)丙烯酸酯、環氧化合物、多官能順丁烯二醯亞胺化合物、及視需要使用之光自由基聚合起始劑或矽烷偶合劑等進行混合之方法等。 As a method of manufacturing the sealant for liquid crystal display elements of the present invention, for example, use of a homogenizer, homomixer, universal mixer, planetary mixer, kneader, three-roll mill, and other mixers to mix epoxy ( Method of mixing meth)acrylate, epoxy compound, polyfunctional maleimide compound, and optionally radical polymerization initiator or silane coupling agent.

可藉由於本發明之液晶顯示元件用密封劑摻合導電性微粒子而製造上下導通材料。另外,此種含有本發明之液晶顯示元件用密封劑及導電性微粒子之上下導通材料亦為本發明之一。 The vertical conduction material can be manufactured by blending conductive fine particles with the sealing compound for liquid crystal display elements of the present invention. In addition, such a top and bottom conduction material containing the sealing compound for liquid crystal display elements of the present invention and conductive fine particles is also one of the present invention.

作為上述導電性微粒子,可使用金屬球、於樹脂微粒子之表面形成有導電金屬層者等。其中,於樹脂微粒子之表面形成有導電金屬層者藉由樹脂微粒子之優異彈性而可於無損透明基板等之情況下導電連接,故而較佳。 As the conductive fine particles, metal balls, those having a conductive metal layer formed on the surface of resin fine particles, or the like can be used. Among them, those with a conductive metal layer formed on the surface of the resin fine particles can be electrically connected without damaging the transparent substrate due to the excellent elasticity of the resin fine particles, and therefore are preferred.

另外,使用本發明之液晶顯示元件用密封劑或本發明之上下導通材料而成之液晶顯示元件亦為本發明之一。 In addition, a liquid crystal display element using the sealant for liquid crystal display elements of the present invention or the top and bottom conduction material of the present invention is also one of the present invention.

作為製造本發明之液晶顯示元件之方法,可較佳地使用液晶滴下法。具體而言,例如可列舉具有如下步驟之方法等:藉由網版印刷、點膠機塗佈等,將本發明之液晶顯示元件用密封劑塗佈於附ITO薄膜等電極之玻璃基板或聚對苯二甲酸乙二酯基板等2片基板之一片上,而形成框 狀之密封圖案;於本發明之液晶顯示元件用密封劑未硬化之狀態下將液晶之微小液滴滴下塗佈於基板之密封圖案之框內,於真空下與另一基板重合;對本發明之液晶顯示元件用密封劑之密封圖案部分照射紫外線等光而使密封劑暫時硬化;及對暫時硬化之密封劑進行加熱而使之正式硬化之步驟。 As a method of manufacturing the liquid crystal display element of the present invention, a liquid crystal dropping method can be preferably used. Specifically, for example, a method having the following steps: by screen printing, dispenser coating, etc., the sealant for liquid crystal display elements of the present invention is applied to a glass substrate with electrodes such as an ITO film or a poly On one of the two substrates such as the ethylene terephthalate substrate, the frame is formed The seal pattern of the shape of the liquid crystal; in the uncured state of the sealant for the liquid crystal display element of the present invention, small droplets of liquid crystal are applied to the frame of the sealing pattern of the substrate, and overlap with another substrate under vacuum; to the present invention The sealing pattern part of the sealing compound for liquid crystal display elements is irradiated with light such as ultraviolet rays to temporarily harden the sealing compound; and the step of heating the temporarily hardened sealing compound to formally harden it.

根據本發明,可提供一種光硬化性、接著性、及防透濕性優異之液晶顯示元件用密封劑。又,根據本發明,可提供一種使用該液晶顯示元件用密封劑而成之上下導通材料及液晶顯示元件。 According to the present invention, it is possible to provide a sealing compound for a liquid crystal display element having excellent photocuring properties, adhesive properties, and moisture permeability. In addition, according to the present invention, it is possible to provide an upper and lower conduction material and a liquid crystal display element using the sealing compound for liquid crystal display elements.

以下,列舉實施例,對本發明進一步詳細地進行說明,但本發明並不僅限定於該等實施例。 Hereinafter, examples are given to explain the present invention in further detail, but the present invention is not limited to these examples.

(實施例1~23、及比較例1~4) (Examples 1 to 23, and Comparative Examples 1 to 4)

依據表1~3所記載之摻合比,使用行星式攪拌機(Thinky公司製造,「去泡攪拌太郎」)將各材料混合後,進而使用三輥研磨機進行混合,藉此製備實施例1~23、及比較例1~4之液晶顯示元件用密封劑。 According to the blending ratios described in Tables 1 to 3, the materials were mixed using a planetary mixer (manufactured by Thinky, "Defoaming Stirring Taro"), and then mixed using a three-roll mill to prepare Examples 1 to 23. And the sealing compound for liquid crystal display elements of Comparative Examples 1 to 4.

再者,作為多官能順丁烯二醯亞胺化合物而記載於表中之聚四亞甲基醚二醇之二順丁烯二醯亞胺乙酸酯(DIC公司製造,「LUMICURE MIA200」) 係上述式(1)所表示之化合物。 Furthermore, the polytetramethylene ether glycol dimaleimide acetate (manufactured by DIC Corporation, "LUMICURE MIA200") listed in the table as a polyfunctional maleimide compound It is a compound represented by the above formula (1).

又,表中之實施例1~23及比較例2~4中之「環氧(甲基)丙烯酸酯與環氧化合物之合計100重量份中,環氧(甲基)丙烯酸酯之含量」係使用上述式(I)而導出。 In addition, the "epoxy (meth)acrylate content in 100 parts by weight of the total of epoxy (meth)acrylate and epoxy compound" in Examples 1 to 23 and Comparative Examples 2 to 4 in the table" It is derived using the above formula (I).

<評價> <evaluation>

對於實施例及比較例中所獲得之液晶顯示元件用密封劑,進行以下之評價。將結果示於表1~3中。 About the sealing compound for liquid crystal display elements obtained by the Example and the comparative example, the following evaluation was performed. The results are shown in Tables 1 to 3.

(光硬化性) (Light hardening)

將實施例及比較例中所獲得之各液晶顯示元件用密封劑以約5μm塗佈於玻璃基板上後,重合相同尺寸之玻璃基板。繼而,使用金屬鹵素燈照射100mW/cm2之光10秒鐘。再者,於照射裝置與玻璃基板之間插入截斷380nm以下之波長之基板。使用紅外分光裝置(BIORAD公司製造,「FTS3000」),對源自丙烯醯基之峰值之光照射前後之變化量(減少率)進行測定。 After each sealing compound for liquid crystal display elements obtained in an Example and a comparative example was apply|coated on the glass substrate in about 5 micrometers, the glass substrates of the same size were laminated|stacked. Then, a metal halide lamp was used to irradiate light of 100 mW/cm 2 for 10 seconds. Furthermore, a substrate that cuts off the wavelength of 380 nm or less is inserted between the irradiation device and the glass substrate. Using an infrared spectrometer (manufactured by BIORAD, "FTS3000"), the amount of change (decrease rate) before and after the light from the peak of the acrylic base was irradiated was measured.

將光照射後之源自丙烯醯基之峰值之減少率為93%以上之情形設為「○」,將75%以上且未達93%之情形設為「△」,將未達75%之情形設為「×」,而對光硬化性進行評價。 If the reduction rate of the peak derived from the acrylic base after light irradiation is 93% or more, set it as "○", if it is 75% or more but less than 93%, it is set as "△", and if it is less than 75% The case was set to "×", and the photocurability was evaluated.

(防透濕性) (Anti-moisture permeability)

利用塗佈機將實施例及比較例中所獲得之各液晶顯示元件用密封劑以成為厚度200~300μm之方式塗佈為平滑之脫模膜狀。繼而,使用金屬鹵素燈照射100mW/cm2之紫外線30秒後,於120℃下加熱60分鐘,藉此獲得透濕度測定用硬化膜。利用依據JIS Z 0208之防濕包裝材料之透濕度試驗 方法(杯突法)的方法製作透濕度試驗用杯,安裝所獲得之透濕度測定用硬化膜,投入至溫度80℃濕度90%RH之恆溫恆濕烘箱內而測定透濕度。將所獲得之透濕度之值未達60g/m2‧24hr之情形設為「○」,將60g/m2‧24hr以上且未達100g/m2‧24hr之情形設為「△」,將為100g/m2‧24hr以上之情形設為「×」,而對防透濕性進行評價。 Each sealing compound for liquid crystal display elements obtained in the Example and the comparative example was coated in the form of a smooth mold release film so that it might become thickness 200-300 micrometers by a coater. Then, a metal halide lamp was used to irradiate 100 mW/cm 2 of ultraviolet rays for 30 seconds, and then heated at 120° C. for 60 minutes to obtain a cured film for measuring moisture permeability. Use the method according to JIS Z 0208 moisture permeability test method (cupping method) to make a moisture permeability test cup, install the obtained cured film for moisture permeability measurement, and put it to a temperature of 80℃ and humidity of 90%RH The moisture permeability is measured in a constant temperature and humidity oven. Set the value obtained when the water vapor permeability is less than 60g/m 2 ‧24hr to "○", and set the value of 60g/m 2 ‧24hr or more and less than 100g/m 2 ‧24hr to "△", and set When it is 100g/m 2 ‧24hr or more, set it as "×", and evaluate the moisture permeability.

(接著性) (Adhesion)

藉由行星式攪拌裝置,使平均粒徑5μm之間隔物粒子(積水化學工業公司製造,「Micropearl SP-2050」)3重量份分散於實施例及比較例中所獲得之各液晶顯示元件用密封劑100重量份中而製成均勻之液。將所獲得之液之極微量取至玻璃基板(20mm×50mm×1.1mmt)之中央部,於其上重合同一類型之玻璃基板而使液晶顯示元件用密封劑擴散開。繼而,使用金屬鹵素燈照射100mW/cm2之紫外線30秒後,於120℃下加熱60分鐘,藉此獲得接著試片。對於所獲得之接著試片,使用張力計對接著強度進行測定。 Using a planetary stirring device, 3 parts by weight of spacer particles (produced by Sekisui Chemical Industry Co., Ltd., "Micropearl SP-2050") with an average particle diameter of 5 μm were dispersed in each of the liquid crystal display elements obtained in the examples and comparative examples. To make a uniform liquid in 100 parts by weight of the agent. A very small amount of the obtained liquid was taken to the center of a glass substrate (20mm×50mm×1.1mmt), and a glass substrate of one type was reconstituted on it to spread the sealant for liquid crystal display elements. Then, a metal halide lamp was used to irradiate 100 mW/cm 2 of ultraviolet rays for 30 seconds, and then heated at 120° C. for 60 minutes, thereby obtaining an adhesive test piece. For the obtained adhesive test piece, the adhesive strength was measured using a tensiometer.

Figure 105132132-A0202-12-0029-7
Figure 105132132-A0202-12-0029-7

Figure 105132132-A0202-12-0030-8
Figure 105132132-A0202-12-0030-8

Figure 105132132-A0202-12-0031-10
Figure 105132132-A0202-12-0031-10

[產業上之利用可能性] [Possibility of industrial use]

根據本發明,可提供一種光硬化性、接著性、及防透濕性優異之液晶顯示元件用密封劑。又,根據本發明,可提供一種使用該液晶顯示元件用密封劑而成之上下導通材料及液晶顯示元件。 According to the present invention, it is possible to provide a sealing compound for a liquid crystal display element having excellent photocuring properties, adhesive properties, and moisture permeability. In addition, according to the present invention, it is possible to provide an upper and lower conduction material and a liquid crystal display element using the sealing compound for liquid crystal display elements.

Claims (5)

一種液晶顯示元件用密封劑,其含有1分子中具有1個以上之(甲基)丙烯醯基之環氧(甲基)丙烯酸酯、1分子中具有1個以上之環氧基之環氧化合物、及1分子中具有2個以上之順丁烯二醯亞胺基之多官能順丁烯二醯亞胺化合物,且上述環氧(甲基)丙烯酸酯與上述環氧化合物之合計100重量份中之上述環氧(甲基)丙烯酸酯之含量超過50重量份且為90重量份以下,上述環氧(甲基)丙烯酸酯含有脂肪族環氧(甲基)丙烯酸酯、或上述環氧化合物含有脂肪族環氧化合物。 A sealing compound for liquid crystal display elements, which contains epoxy (meth)acrylate having one or more (meth)acrylic groups in one molecule, and epoxy compound having one or more epoxy groups in one molecule , And a polyfunctional maleimide compound having two or more maleimide groups in one molecule, and the total of the above-mentioned epoxy (meth)acrylate and the above-mentioned epoxy compound is 100 parts by weight The content of the epoxy (meth)acrylate is more than 50 parts by weight and 90 parts by weight or less, and the epoxy (meth)acrylate contains aliphatic epoxy (meth)acrylate or the epoxy compound Contains aliphatic epoxy compounds. 如申請專利範圍第1項之液晶顯示元件用密封劑,其含有光自由基聚合起始劑。 For example, the sealing compound for liquid crystal display elements of the first item in the scope of patent application contains a photoradical polymerization initiator. 如申請專利範圍第2項之液晶顯示元件用密封劑,其含有光自由基聚合起始劑、及熱自由基聚合起始劑或硬化促進劑。 For example, the sealing compound for liquid crystal display elements of the second item of the scope of patent application contains a light radical polymerization initiator, and a thermal radical polymerization initiator or hardening accelerator. 一種上下導通材料,其含有申請專利範圍第1、2或3項之液晶顯示元件用密封劑及導電性微粒子。 An up-and-down conduction material, which contains the sealing compound for liquid crystal display elements of the first, second or third patent application range and conductive particles. 一種液晶顯示元件,其使用申請專利範圍第1、2或3項之液晶顯示元件用密封劑或申請專利範圍第4項之上下導通材料而形成。 A liquid crystal display element, which is formed using the sealant for liquid crystal display elements of the first, second, or third patent range or the upper and lower conductive material of the fourth patent range.
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