WO2007074781A1 - 液晶シール剤およびこれを用いた液晶パネルの製造方法 - Google Patents
液晶シール剤およびこれを用いた液晶パネルの製造方法 Download PDFInfo
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- WO2007074781A1 WO2007074781A1 PCT/JP2006/325797 JP2006325797W WO2007074781A1 WO 2007074781 A1 WO2007074781 A1 WO 2007074781A1 JP 2006325797 W JP2006325797 W JP 2006325797W WO 2007074781 A1 WO2007074781 A1 WO 2007074781A1
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- Prior art keywords
- liquid crystal
- epoxy resin
- group
- sealant
- mass
- Prior art date
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- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
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- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
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- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000012769 display material Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
- 229940091173 hydantoin Drugs 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- ARZLUCYKIWYSHR-UHFFFAOYSA-N hydroxymethoxymethanol Chemical compound OCOCO ARZLUCYKIWYSHR-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000005040 ion trap Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000000199 molecular distillation Methods 0.000 description 1
- UUORTJUPDJJXST-UHFFFAOYSA-N n-(2-hydroxyethyl)prop-2-enamide Chemical compound OCCNC(=O)C=C UUORTJUPDJJXST-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940117969 neopentyl glycol Drugs 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- OTLDLKLSNZMTTA-UHFFFAOYSA-N octahydro-1h-4,7-methanoindene-1,5-diyldimethanol Chemical compound C1C2C3C(CO)CCC3C1C(CO)C2 OTLDLKLSNZMTTA-UHFFFAOYSA-N 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
-
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/10—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers containing more than one epoxy radical 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
- 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
- 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
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- 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 object of the present invention is excellent in adhesion resistance and adhesion reliability after being left for a long time under high temperature and high humidity, electro-optical properties of liquid crystal, and moisture resistance reliability such as liquid crystal alignment maintenance, and the liquid crystal panel.
- An object of the present invention is to provide a liquid crystal sealant having excellent viscosity stability when applied to a substrate.
- X is a single bond, an alkylene group, or a group represented by the formula (A) or (B))
- R is an alkylene group
- R is a polymerizable functional group
- X is a single bond (a structure in which carbon of a carboxyl group and oxygen of a phenoxy group are directly bonded), a group represented by formula (A) or formula (B).
- A a structure in which carbon of a carboxyl group and oxygen of a phenoxy group are directly bonded
- B a group represented by formula (B) or formula (B).
- Aliphatic polyvalent glycidyl ester compound obtained by reaction of aliphatic dicarboxylic acid typified by adipic acid, itaconic acid, etc. and epichlorohydrin, isophthalic acid, terephthalic acid, pyromellitic acid It was obtained by the reaction of aromatic polycarboxylic acid ester compound obtained by the reaction of aromatic dicarboxylic acid and epichlorohydrin typified by etc., and hydroxydicarboxylic acid compound and epichlorohydrin. Aliphatic polyvalent glycidyl ether ester compound or aromatic polyvalent glycidyl ether ester compound.
- Aromatic diols typified by bisphenol AD, etc. and glycidyl ether compounds that can also produce epichlorohydrin power, or aromatic diamines typified by diaminodimethane, arrin, and xylylenediamine.
- Aromatic polyvalent glycidylamine compounds obtained by reaction with epichlorohydrin are preferred.
- N-Buyl 1-Pyrrolidone Ataliloylmorpholine, Bulleimidazole, N-Bilcaprolatatam, Buelacetate, (Meth) acrylic acid, (Meth) acrylamide, N-Hydroxymethylacrylamide or N-Hydroxyethylacrylamide And their alkyl ether compounds.
- Bisphenol A type epoxy resin Epiclon EXA850CRP (Epoxy equivalent 190gZeq manufactured by Dainippon Ink & Chemicals, Inc.) 346g (epoxy group) in a 500ml four-necked flask equipped with a stirrer, gas inlet tube, thermometer, and condenser tube 1.82 mol), phenol metatalylate (ester group equivalent 162 gZeq) 162 g (1.0 mol ester group), tetraptyl ammonium bromide 16 g, hydroquinone monomethyl ether 0.1 g. Subsequently, the reaction was conducted by heating and stirring at 120 ° C. for 8 hours while publishing with dry air to obtain a modified epoxy resin (partially phenylmethacrylate epoxy resin). The obtained rosin was washed with ultrapure water.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Physics & Mathematics (AREA)
- Nonlinear Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mathematical Physics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Sealing Material Composition (AREA)
- Epoxy Resins (AREA)
- Liquid Crystal (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2006800437799A CN101313244B (zh) | 2005-12-27 | 2006-12-25 | 液晶密封剂及使用其的液晶面板的制造方法 |
| JP2007551963A JP5032340B2 (ja) | 2005-12-27 | 2006-12-25 | 液晶シール剤およびこれを用いた液晶パネルの製造方法 |
| HK09104509.7A HK1126285B (en) | 2005-12-27 | 2006-12-25 | Sealing material for liquid crystals and process for production of liquid crystal panels with the same |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2005-373643 | 2005-12-27 | ||
| JP2005373643 | 2005-12-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2007074781A1 true WO2007074781A1 (ja) | 2007-07-05 |
Family
ID=38218001
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2006/325797 WO2007074781A1 (ja) | 2005-12-27 | 2006-12-25 | 液晶シール剤およびこれを用いた液晶パネルの製造方法 |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JP5032340B2 (enrdf_load_stackoverflow) |
| KR (1) | KR100980546B1 (enrdf_load_stackoverflow) |
| CN (1) | CN101313244B (enrdf_load_stackoverflow) |
| TW (1) | TW200728873A (enrdf_load_stackoverflow) |
| WO (1) | WO2007074781A1 (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012073633A1 (ja) * | 2010-11-30 | 2012-06-07 | Dic株式会社 | カチオン重合性樹脂組成物、それを用いて得られる光学用材料、積層体 |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101134635B1 (ko) * | 2009-10-12 | 2012-04-09 | 금호석유화학 주식회사 | 액정 표시 소자용 실란트 조성물 |
| WO2020145262A1 (ja) * | 2019-01-10 | 2020-07-16 | 三菱ケミカル株式会社 | 変性エポキシ樹脂、エポキシ樹脂組成物、硬化物、及び電気・電子回路用積層板 |
| KR20220123442A (ko) * | 2020-03-02 | 2022-09-06 | 미쓰이 가가쿠 가부시키가이샤 | 액정 적하 공법용 실링제 및 액정 표시 패널의 제조 방법 |
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| JPS62207241A (ja) * | 1986-03-07 | 1987-09-11 | Tatatomi Nishikubo | アクリロイル基及び／またはメタクリロイル基含有化合物の製造方法 |
| JPH03188186A (ja) * | 1989-12-19 | 1991-08-16 | Toshiba Corp | シール剤組成物及び液晶表示パネル |
| JPH05156196A (ja) * | 1991-11-29 | 1993-06-22 | Dainippon Printing Co Ltd | 紫外線硬化性印刷インキ |
| JPH07292067A (ja) * | 1994-04-27 | 1995-11-07 | Yuka Shell Epoxy Kk | 変性エポキシ樹脂の製造方法と製造された変性エポキシ樹脂及びこのエポキシ樹脂の組成物 |
| JPH09194567A (ja) * | 1996-01-25 | 1997-07-29 | Namitsukusu Kk | 液晶表示セル用シール剤およびそれを用いた液晶表示セル |
| JP2005308811A (ja) * | 2004-04-16 | 2005-11-04 | Sekisui Chem Co Ltd | 液晶表示素子用熱硬化性樹脂組成物、液晶滴下工法用シール剤、上下導通材料及び液晶表示素子 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62207309A (ja) * | 1986-03-07 | 1987-09-11 | Tatatomi Nishikubo | 光硬化性組成物 |
| JPH1114802A (ja) * | 1997-06-26 | 1999-01-22 | Seiko Epson Corp | 光学用樹脂組成物及び光学用樹脂 |
| KR20010080093A (ko) * | 1999-08-12 | 2001-08-22 | 사토 아키오 | 실링제용광경화형수지조성물 및 실링방법. |
| US7566377B2 (en) * | 2002-09-19 | 2009-07-28 | Mitsui Chemicals, Inc. | Liquid crystal sealing agent composition and manufacturing method of liquid crystal display panel using the same |
-
2006
- 2006-12-25 CN CN2006800437799A patent/CN101313244B/zh active Active
- 2006-12-25 JP JP2007551963A patent/JP5032340B2/ja active Active
- 2006-12-25 KR KR1020087015573A patent/KR100980546B1/ko active Active
- 2006-12-25 WO PCT/JP2006/325797 patent/WO2007074781A1/ja active Application Filing
- 2006-12-26 TW TW095148923A patent/TW200728873A/zh unknown
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62207241A (ja) * | 1986-03-07 | 1987-09-11 | Tatatomi Nishikubo | アクリロイル基及び／またはメタクリロイル基含有化合物の製造方法 |
| JPH03188186A (ja) * | 1989-12-19 | 1991-08-16 | Toshiba Corp | シール剤組成物及び液晶表示パネル |
| JPH05156196A (ja) * | 1991-11-29 | 1993-06-22 | Dainippon Printing Co Ltd | 紫外線硬化性印刷インキ |
| JPH07292067A (ja) * | 1994-04-27 | 1995-11-07 | Yuka Shell Epoxy Kk | 変性エポキシ樹脂の製造方法と製造された変性エポキシ樹脂及びこのエポキシ樹脂の組成物 |
| JPH09194567A (ja) * | 1996-01-25 | 1997-07-29 | Namitsukusu Kk | 液晶表示セル用シール剤およびそれを用いた液晶表示セル |
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| WO2012073633A1 (ja) * | 2010-11-30 | 2012-06-07 | Dic株式会社 | カチオン重合性樹脂組成物、それを用いて得られる光学用材料、積層体 |
| JP5013029B2 (ja) * | 2010-11-30 | 2012-08-29 | Ｄｉｃ株式会社 | カチオン重合性樹脂組成物、それを用いて得られる光学用材料、積層体 |
Also Published As
| Publication number | Publication date |
|---|---|
| TW200728873A (en) | 2007-08-01 |
| KR20080078857A (ko) | 2008-08-28 |
| CN101313244B (zh) | 2010-04-21 |
| TWI354169B (enrdf_load_stackoverflow) | 2011-12-11 |
| JP5032340B2 (ja) | 2012-09-26 |
| JPWO2007074781A1 (ja) | 2009-06-04 |
| KR100980546B1 (ko) | 2010-09-06 |
| CN101313244A (zh) | 2008-11-26 |
| HK1126285A1 (zh) | 2009-08-28 |
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