JP5459483B2 - 熱硬化膜形成用ポリエステル樹脂溶液 - Google Patents
熱硬化膜形成用ポリエステル樹脂溶液 Download PDFInfo
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- JP5459483B2 JP5459483B2 JP2009538140A JP2009538140A JP5459483B2 JP 5459483 B2 JP5459483 B2 JP 5459483B2 JP 2009538140 A JP2009538140 A JP 2009538140A JP 2009538140 A JP2009538140 A JP 2009538140A JP 5459483 B2 JP5459483 B2 JP 5459483B2
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- TXXACRDXEHKXKD-UHFFFAOYSA-M benzyl(trimethyl)phosphanium;chloride Chemical compound [Cl-].C[P+](C)(C)CC1=CC=CC=C1 TXXACRDXEHKXKD-UHFFFAOYSA-M 0.000 description 1
- OSPKGDDLQQVQSG-UHFFFAOYSA-M benzyl(tripropyl)azanium;bromide Chemical compound [Br-].CCC[N+](CCC)(CCC)CC1=CC=CC=C1 OSPKGDDLQQVQSG-UHFFFAOYSA-M 0.000 description 1
- YTRIOKYQEVFKGU-UHFFFAOYSA-M benzyl(tripropyl)azanium;chloride Chemical compound [Cl-].CCC[N+](CCC)(CCC)CC1=CC=CC=C1 YTRIOKYQEVFKGU-UHFFFAOYSA-M 0.000 description 1
- RVRYXDDGQFDMBL-UHFFFAOYSA-M benzyl(tripropyl)phosphanium;bromide Chemical compound [Br-].CCC[P+](CCC)(CCC)CC1=CC=CC=C1 RVRYXDDGQFDMBL-UHFFFAOYSA-M 0.000 description 1
- DDLBXRNAWNFTAE-UHFFFAOYSA-M benzyl(tripropyl)phosphanium;chloride Chemical compound [Cl-].CCC[P+](CCC)(CCC)CC1=CC=CC=C1 DDLBXRNAWNFTAE-UHFFFAOYSA-M 0.000 description 1
- GKLBCPASXYEUFD-UHFFFAOYSA-N bicyclo[2.2.2]oct-en-2,3-dicarboxylic anhydride Chemical compound C1CC2C3C(=O)OC(=O)C3=C1CC2 GKLBCPASXYEUFD-UHFFFAOYSA-N 0.000 description 1
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- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
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- PMMYEEVYMWASQN-IMJSIDKUSA-N cis-4-Hydroxy-L-proline Chemical compound O[C@@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-IMJSIDKUSA-N 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- RZIPTXDCNDIINL-UHFFFAOYSA-N cyclohexane-1,1,2,2-tetracarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCCCC1(C(O)=O)C(O)=O RZIPTXDCNDIINL-UHFFFAOYSA-N 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
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- WHRLOJCOIKOQGL-UHFFFAOYSA-N ethyl 2-methoxypropanoate Chemical compound CCOC(=O)C(C)OC WHRLOJCOIKOQGL-UHFFFAOYSA-N 0.000 description 1
- BHXIWUJLHYHGSJ-UHFFFAOYSA-N ethyl 3-ethoxypropanoate Chemical compound CCOCCC(=O)OCC BHXIWUJLHYHGSJ-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
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- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- BDJSOPWXYLFTNW-UHFFFAOYSA-N methyl 3-methoxypropanoate Chemical compound COCCC(=O)OC BDJSOPWXYLFTNW-UHFFFAOYSA-N 0.000 description 1
- KNRCVAANTQNTPT-UHFFFAOYSA-N methyl-5-norbornene-2,3-dicarboxylic anhydride Chemical compound O=C1OC(=O)C2C1C1(C)C=CC2C1 KNRCVAANTQNTPT-UHFFFAOYSA-N 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 239000012299 nitrogen atmosphere 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
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- WAGFXJQAIZNSEQ-UHFFFAOYSA-M tetraphenylphosphonium chloride Chemical compound [Cl-].C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 WAGFXJQAIZNSEQ-UHFFFAOYSA-M 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Images
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
-
- 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
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/04—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyesters
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/123—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
- C08G63/21—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups in the presence of unsaturated monocarboxylic acids or unsaturated monohydric alcohols or reactive derivatives thereof
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- 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
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
- G02F1/133509—Filters, e.g. light shielding masks
- G02F1/133514—Colour filters
- G02F1/133519—Overcoatings
-
- 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
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/133711—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films
-
- 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
- G02F2202/00—Materials and properties
- G02F2202/02—Materials and properties organic material
- G02F2202/022—Materials and properties organic material polymeric
- G02F2202/023—Materials and properties organic material polymeric curable
- G02F2202/025—Materials and properties organic material polymeric curable thermocurable
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Optical Filters (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
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JP2009538140A JP5459483B2 (ja) | 2007-10-19 | 2008-10-16 | 熱硬化膜形成用ポリエステル樹脂溶液 |
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WO2016031094A1 (ja) * | 2014-08-27 | 2016-03-03 | Ykk株式会社 | ファスナーストリンガー及びそれを備えたスライドファスナー |
CN107390420A (zh) * | 2017-08-02 | 2017-11-24 | 京东方科技集团股份有限公司 | 一种彩膜基板及显示装置 |
CN107286333B (zh) * | 2017-08-07 | 2019-02-15 | 南方医科大学南方医院 | 一种抗菌不饱和脂肪族聚酯及其制备方法和应用 |
Citations (9)
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---|---|---|---|---|
JPS531284A (en) * | 1977-05-30 | 1978-01-09 | Nok Corp | Photosensitive compositions |
JPS6461746A (en) * | 1987-09-02 | 1989-03-08 | Hitachi Ltd | Heat-resisting photosensitive polymer composition |
JPH02178370A (ja) * | 1988-12-29 | 1990-07-11 | Toyo Ink Mfg Co Ltd | 熱硬化性塗料 |
WO2003072634A1 (fr) * | 2002-02-26 | 2003-09-04 | Nippon Kayaku Kabushiki Kaisha | Resines photosensibles, compositions de resine et produits pour les faire durcir |
JP2005105264A (ja) * | 2003-09-09 | 2005-04-21 | Chisso Corp | 熱硬化性樹脂組成物及び硬化膜 |
JP2006003860A (ja) * | 2003-11-26 | 2006-01-05 | Nippon Steel Chem Co Ltd | 感光性樹脂組成物及びそれを用いたカラーフィルター |
JP2006521452A (ja) * | 2003-03-24 | 2006-09-21 | エルジー・ケム・リミテッド | 高耐熱性透明ポリイミド前駆体及びそれの感光性ポリイミド組成物 |
JP2006282995A (ja) * | 2005-03-08 | 2006-10-19 | Chisso Corp | 熱硬化性重合体組成物 |
JP2007094164A (ja) * | 2005-09-29 | 2007-04-12 | Dainippon Printing Co Ltd | 液晶表示装置用硬化膜 |
Family Cites Families (2)
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---|---|---|---|---|
JPS5146559B2 (ko) * | 1973-08-20 | 1976-12-09 | ||
JPS5388097A (en) * | 1977-03-04 | 1978-08-03 | Nitto Electric Ind Co Ltd | Epoxy resin composition |
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- 2008-10-16 WO PCT/JP2008/068767 patent/WO2009051187A1/ja active Application Filing
- 2008-10-16 CN CN201310561221.1A patent/CN103709911A/zh active Pending
- 2008-10-16 JP JP2009538140A patent/JP5459483B2/ja active Active
- 2008-10-16 CN CN200880109757A patent/CN101809060A/zh active Pending
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Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS531284A (en) * | 1977-05-30 | 1978-01-09 | Nok Corp | Photosensitive compositions |
JPS6461746A (en) * | 1987-09-02 | 1989-03-08 | Hitachi Ltd | Heat-resisting photosensitive polymer composition |
JPH02178370A (ja) * | 1988-12-29 | 1990-07-11 | Toyo Ink Mfg Co Ltd | 熱硬化性塗料 |
WO2003072634A1 (fr) * | 2002-02-26 | 2003-09-04 | Nippon Kayaku Kabushiki Kaisha | Resines photosensibles, compositions de resine et produits pour les faire durcir |
JP2006521452A (ja) * | 2003-03-24 | 2006-09-21 | エルジー・ケム・リミテッド | 高耐熱性透明ポリイミド前駆体及びそれの感光性ポリイミド組成物 |
JP2005105264A (ja) * | 2003-09-09 | 2005-04-21 | Chisso Corp | 熱硬化性樹脂組成物及び硬化膜 |
JP2006003860A (ja) * | 2003-11-26 | 2006-01-05 | Nippon Steel Chem Co Ltd | 感光性樹脂組成物及びそれを用いたカラーフィルター |
JP2006282995A (ja) * | 2005-03-08 | 2006-10-19 | Chisso Corp | 熱硬化性重合体組成物 |
JP2007094164A (ja) * | 2005-09-29 | 2007-04-12 | Dainippon Printing Co Ltd | 液晶表示装置用硬化膜 |
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JPWO2009051187A1 (ja) | 2011-03-03 |
TWI444395B (zh) | 2014-07-11 |
WO2009051187A1 (ja) | 2009-04-23 |
KR20100099118A (ko) | 2010-09-10 |
KR101472070B1 (ko) | 2014-12-15 |
CN103709911A (zh) | 2014-04-09 |
CN101809060A (zh) | 2010-08-18 |
TW200936618A (en) | 2009-09-01 |
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