TWI691567B - 黏接劑組成物及使用該組成物形成之黏接劑與偏光板用黏接劑 - Google Patents

黏接劑組成物及使用該組成物形成之黏接劑與偏光板用黏接劑 Download PDF

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Publication number: TWI691567B
Authority: TW; Taiwan
Prior art keywords: meth; acrylate; acrylic resin; adhesive; monomer
Prior art date: 2014-07-18

Application number

TW104123180A

Other languages

English (en)

Chinese (zh)

Other versions

TW201631091A (zh

Inventor

三谷直也

中島貴弘

山中淳司

Original Assignee

三菱化學股份有限公司

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2014-07-18

Filing date

2015-07-17

Publication date

2020-04-21

2015-07-17 Application filed by 三菱化學股份有限公司 filed Critical 三菱化學股份有限公司

2016-09-01 Publication of TW201631091A publication Critical patent/TW201631091A/zh

2020-04-21 Application granted granted Critical

2020-04-21 Publication of TWI691567B publication Critical patent/TWI691567B/zh

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230000001070 adhesive effect Effects 0.000 title claims description 99
239000000853 adhesive Substances 0.000 title claims description 96
239000000203 mixture Substances 0.000 title claims description 54
239000000178 monomer Substances 0.000 claims description 155
239000004925 Acrylic resin Substances 0.000 claims description 123
229920000178 Acrylic resin Polymers 0.000 claims description 123
239000003431 cross linking reagent Substances 0.000 claims description 56
125000000524 functional group Chemical group 0.000 claims description 53
238000006116 polymerization reaction Methods 0.000 claims description 25
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 20
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 13
239000004593 Epoxy Substances 0.000 claims description 10
238000004132 cross linking Methods 0.000 claims description 10
125000003368 amide group Chemical group 0.000 claims description 9
239000012948 isocyanate Substances 0.000 claims description 7
150000002513 isocyanates Chemical class 0.000 claims description 7
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 162
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 120
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical group N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 88
-1 triethyl acetyl Chemical group 0.000 description 77
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 66
239000012790 adhesive layer Substances 0.000 description 36
239000010408 film Substances 0.000 description 29
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 28
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 28
238000010992 reflux Methods 0.000 description 28
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 24
230000007423 decrease Effects 0.000 description 24
239000000243 solution Substances 0.000 description 24
239000006185 dispersion Substances 0.000 description 23
230000009477 glass transition Effects 0.000 description 23
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 22
238000000034 method Methods 0.000 description 21
230000003287 optical effect Effects 0.000 description 21
238000012360 testing method Methods 0.000 description 21
239000006087 Silane Coupling Agent Substances 0.000 description 20
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 19
229910052757 nitrogen Inorganic materials 0.000 description 18
239000003505 polymerization initiator Substances 0.000 description 18
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 16
238000011156 evaluation Methods 0.000 description 16
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
239000011521 glass Substances 0.000 description 15
239000007787 solid Substances 0.000 description 15
238000001035 drying Methods 0.000 description 14
125000000217 alkyl group Chemical group 0.000 description 13
GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 description 13
238000004519 manufacturing process Methods 0.000 description 12
239000011347 resin Substances 0.000 description 12
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OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 10
WHNPOQXWAMXPTA-UHFFFAOYSA-N 3-methylbut-2-enamide Chemical compound CC(C)=CC(N)=O WHNPOQXWAMXPTA-UHFFFAOYSA-N 0.000 description 9
239000004973 liquid crystal related substance Substances 0.000 description 9
239000002904 solvent Substances 0.000 description 9
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 8
239000004372 Polyvinyl alcohol Substances 0.000 description 8
125000002723 alicyclic group Chemical group 0.000 description 8
239000002216 antistatic agent Substances 0.000 description 8
125000003118 aryl group Chemical group 0.000 description 8
230000000052 comparative effect Effects 0.000 description 8
125000001033 ether group Chemical group 0.000 description 8
229920002451 polyvinyl alcohol Polymers 0.000 description 8
238000010526 radical polymerization reaction Methods 0.000 description 8
229910052751 metal Inorganic materials 0.000 description 7
239000002184 metal Substances 0.000 description 7
230000000379 polymerizing effect Effects 0.000 description 7
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QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
239000002202 Polyethylene glycol Substances 0.000 description 6
125000003277 amino group Chemical group 0.000 description 6
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
238000002156 mixing Methods 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
229920001223 polyethylene glycol Polymers 0.000 description 6
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 6
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
150000001412 amines Chemical class 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
239000010410 layer Substances 0.000 description 5
239000000463 material Substances 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
238000003860 storage Methods 0.000 description 5
239000008096 xylene Substances 0.000 description 5
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
229920000877 Melamine resin Polymers 0.000 description 4
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
150000001299 aldehydes Chemical class 0.000 description 4
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
238000012662 bulk polymerization Methods 0.000 description 4
FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
230000007547 defect Effects 0.000 description 4
125000003700 epoxy group Chemical group 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 4
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 4
238000005259 measurement Methods 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
150000003512 tertiary amines Chemical group 0.000 description 4
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 4
BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 4
HLIQLHSBZXDKLV-UHFFFAOYSA-N 2-(2-hydroxyethoxy)-1-phenoxyethanol Chemical compound OCCOCC(O)OC1=CC=CC=C1 HLIQLHSBZXDKLV-UHFFFAOYSA-N 0.000 description 3
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
239000004743 Polypropylene Substances 0.000 description 3
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 3
229940081735 acetylcellulose Drugs 0.000 description 3
150000001252 acrylic acid derivatives Chemical class 0.000 description 3
150000001336 alkenes Chemical class 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
229920002301 cellulose acetate Polymers 0.000 description 3
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238000000576 coating method Methods 0.000 description 3
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210000002858 crystal cell Anatomy 0.000 description 3
150000001925 cycloalkenes Chemical class 0.000 description 3
MAWOHFOSAIXURX-UHFFFAOYSA-N cyclopentylcyclopentane Chemical group C1CCCC1C1CCCC1 MAWOHFOSAIXURX-UHFFFAOYSA-N 0.000 description 3
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000945 filler Substances 0.000 description 3
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229910052739 hydrogen Inorganic materials 0.000 description 3
239000012535 impurity Substances 0.000 description 3
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
150000002825 nitriles Chemical class 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
229920000573 polyethylene Polymers 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
229920001155 polypropylene Polymers 0.000 description 3
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 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
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 3
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239000003643 water by type Substances 0.000 description 3
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YHYCMHWTYHPIQS-UHFFFAOYSA-N 2-(2-hydroxyethoxy)-1-methoxyethanol Chemical compound COC(O)COCCO YHYCMHWTYHPIQS-UHFFFAOYSA-N 0.000 description 2
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 2
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
WWUCYCYSEUEANO-UHFFFAOYSA-N 2-(aziridin-1-yl)acetamide Chemical compound NC(=O)CN1CC1 WWUCYCYSEUEANO-UHFFFAOYSA-N 0.000 description 2
KLAXJOVIZWGVJE-UHFFFAOYSA-N 2-butoxy-2-(2-hydroxyethoxy)ethanol Chemical compound CCCCOC(CO)OCCO KLAXJOVIZWGVJE-UHFFFAOYSA-N 0.000 description 2
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 2
VFXXTYGQYWRHJP-UHFFFAOYSA-N 4,4'-azobis(4-cyanopentanoic acid) Chemical compound OC(=O)CCC(C)(C#N)N=NC(C)(CCC(O)=O)C#N VFXXTYGQYWRHJP-UHFFFAOYSA-N 0.000 description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 2
239000004342 Benzoyl peroxide Substances 0.000 description 2
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
229920002284 Cellulose triacetate Polymers 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
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235000017858 Laurus nobilis Nutrition 0.000 description 2
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 2
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
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229910019142 PO4 Inorganic materials 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
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NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
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125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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239000012969 di-tertiary-butyl peroxide Substances 0.000 description 2
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000009826 distribution Methods 0.000 description 2
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AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 2
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JGEMYUOFGVHXKV-OWOJBTEDSA-N fumaraldehyde Chemical compound O=C\C=C\C=O JGEMYUOFGVHXKV-OWOJBTEDSA-N 0.000 description 2
239000007789 gas Substances 0.000 description 2
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238000010438 heat treatment Methods 0.000 description 2
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
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230000006872 improvement Effects 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
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229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
MHEBVKPOSBNNAC-UHFFFAOYSA-N potassium;bis(fluorosulfonyl)azanide Chemical compound [K+].FS(=O)(=O)[N-]S(F)(=O)=O MHEBVKPOSBNNAC-UHFFFAOYSA-N 0.000 description 1
125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
230000002265 prevention Effects 0.000 description 1
AXLMPTNTPOWPLT-UHFFFAOYSA-N prop-2-enyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCC=C AXLMPTNTPOWPLT-UHFFFAOYSA-N 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
125000005767 propoxymethyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])[#8]C([H])([H])* 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000011002 quantification Methods 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
230000005855 radiation Effects 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
238000007650 screen-printing Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
230000001568 sexual effect Effects 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
241000894007 species Species 0.000 description 1
230000003068 static effect Effects 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
230000001629 suppression Effects 0.000 description 1
230000008961 swelling Effects 0.000 description 1
125000001302 tertiary amino group Chemical group 0.000 description 1
238000010998 test method Methods 0.000 description 1
125000005207 tetraalkylammonium group Chemical group 0.000 description 1
LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
229920002803 thermoplastic polyurethane Polymers 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
239000011135 tin Substances 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
IJFSHBYRKXAYFV-UHFFFAOYSA-N triethoxy(3-propoxypropyl)silane Chemical compound CCCOCCC[Si](OCC)(OCC)OCC IJFSHBYRKXAYFV-UHFFFAOYSA-N 0.000 description 1
JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
TZYULTYGSBAILI-UHFFFAOYSA-M trimethyl(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC=C TZYULTYGSBAILI-UHFFFAOYSA-M 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052726 zirconium Inorganic materials 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
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Optics & Photonics (AREA)
Adhesives Or Adhesive Processes (AREA)
Adhesive Tapes (AREA)
Polarising Elements (AREA)

TW104123180A 2014-07-18 2015-07-17 黏接劑組成物及使用該組成物形成之黏接劑與偏光板用黏接劑 TWI691567B (zh)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP2014-147865		2014-07-18
JP2014147865		2014-07-18

Publications (2)

Publication Number	Publication Date
TW201631091A TW201631091A (zh)	2016-09-01
TWI691567B true TWI691567B (zh)	2020-04-21

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Country Status (5)

Country	Link
JP (1)	JP6657948B2 (fr)
KR (1)	KR102301157B1 (fr)
CN (1)	CN106661406B (fr)
TW (1)	TWI691567B (fr)
WO (1)	WO2016010140A1 (fr)

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WO2018034230A1 (fr) *	2016-08-17	2018-02-22	日本合成化学工業株式会社	Composition d'adhésif acrylique, adhésif constitué à l'aide de celle-ci, adhésif pour plaque de polarisation, et dispositif d'affichage d'image
JP6875011B2 (ja) *	2016-09-20	2021-05-19	リンテック株式会社	半導体加工用粘着シート
JP6899339B2 (ja) *	2018-01-24	2021-07-07	日東電工株式会社	表面保護フィルムおよび保護フィルム付き光学部材
KR102259745B1 (ko)	2018-12-07	2021-06-02	주식회사 엘지화학	점착 수지 및 이를 포함하는 광학부재용 점착제 조성물

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TW201241124A (en) *	2011-02-02	2012-10-16	Soken Kagaku Kk	Adhesive agent composition for optical film and processed product of the same

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JP4635150B2 (ja) *	2004-04-14	2011-02-16	綜研化学株式会社	光学部材用粘着剤組成物および光学部材用粘着フィルム、ならびにこれらを用いた光学部材
TW200636032A (en) *	2005-04-13	2006-10-16	Lg Chemical Ltd	Acrylic adhesive composition having excellent impact resistance, optical film using the adhesive composition, and liquid crystal display comprising the optical film
KR100784995B1 (ko)	2005-09-05	2007-12-11	주식회사 엘지화학	편광판용 아크릴계 점착제 조성물
KR100932887B1 (ko) *	2005-12-14	2009-12-21	주식회사 엘지화학	아크릴계 점착제 조성물
CN101490195B (zh) *	2006-07-20	2011-11-09	综研化学株式会社	Pdp前滤膜用胶粘剂组合物及用途
JP2009126929A (ja) *	2007-11-22	2009-06-11	Cheil Industries Inc	粘着剤組成物及び光学部材、表面保護シート
JP5361244B2 (ja) *	2008-05-15	2013-12-04	日本カーバイド工業株式会社	光学部材表面保護フィルム用粘着剤組成物及び光学部材表面保護フィルム
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2015
- 2015-07-17 WO PCT/JP2015/070537 patent/WO2016010140A1/fr not_active Ceased
- 2015-07-17 JP JP2015536329A patent/JP6657948B2/ja active Active
- 2015-07-17 TW TW104123180A patent/TWI691567B/zh active
- 2015-07-17 CN CN201580039371.3A patent/CN106661406B/zh active Active
- 2015-07-17 KR KR1020177001442A patent/KR102301157B1/ko active Active

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TW201241124A (en) *	2011-02-02	2012-10-16	Soken Kagaku Kk	Adhesive agent composition for optical film and processed product of the same

Also Published As

Publication number	Publication date
JPWO2016010140A1 (ja)	2017-04-27
CN106661406B (zh)	2020-12-15
JP6657948B2 (ja)	2020-03-04
KR20170032313A (ko)	2017-03-22
WO2016010140A1 (fr)	2016-01-21
TW201631091A (zh)	2016-09-01
KR102301157B1 (ko)	2021-09-10
CN106661406A (zh)	2017-05-10

Publication	Publication Date	Title
TWI575045B (zh)	2017-03-21	Adhesive composition for optical member, Adhesive for optical member, Optical member with adhesive layer, and image display device
JP6042036B1 (ja)	2016-12-14	粘着剤組成物、およびそれを用いてなる粘着剤並びに偏光板用粘着剤
JP7137159B2 (ja)	2022-09-14	アクリル系粘着剤組成物、及びそれを用いてなる粘着剤、偏光板用粘着剤、ならびに画像表示装置
JP2012077299A (ja)	2012-04-19	粘着剤組成物、粘着剤、光学部材用粘着剤、粘着剤層付き光学部材、画像表示装置
JP6950530B2 (ja)	2021-10-13	アクリル系粘着剤組成物、及びそれを用いてなる粘着剤、偏光板用粘着剤、ならびに画像表示装置
JP2017160383A (ja)	2017-09-14	粘着剤組成物及び粘着シート
TWI691567B (zh)	2020-04-21	黏接劑組成物及使用該組成物形成之黏接劑與偏光板用黏接劑
JP6950531B2 (ja)	2021-10-13	アクリル系粘着剤組成物、及びそれを用いてなる粘着剤、偏光板用粘着剤、ならびに画像表示装置
JPWO2018084008A1 (ja)	2019-09-19	偏光板用粘着剤組成物、偏光板用粘着剤、並びに粘着剤層付偏光板
JP6859937B2 (ja)	2021-04-14	粘着剤組成物、およびそれを用いてなる偏光板用粘着剤、粘着剤層付偏光板、ならびに画像表示装置
JP2013199579A (ja)	2013-10-03	アクリル系粘着剤、光学部材用粘着剤、およびそれを用いてなる粘着剤層付き光学部材、画像表示装置、ならびにアクリル系粘着剤の製造方法、アクリル系粘着剤組成物
JP6708017B2 (ja)	2020-06-10	粘着剤組成物、およびそれを用いてなる粘着剤並びに偏光板用粘着剤
JP7119972B2 (ja)	2022-08-17	粘着剤組成物及びそれを用いてなる粘着剤、偏光板用粘着剤、ならびに画像表示装置
JP2019031586A (ja)	2019-02-28	粘着剤組成物、およびそれを用いてなる粘着剤、偏光板用粘着剤、ならびに画像表示装置
JP6776754B2 (ja)	2020-10-28	偏光板用粘着剤組成物、偏光板用粘着剤、粘着剤層付偏光板並びに離型フィルム付粘着剤層付偏光板
JP2021143286A (ja)	2021-09-24	粘着剤組成物、その粘着剤組成物を用いてなる粘着剤、ならびにその粘着剤を用いた偏光板用粘着剤及び画像表示装置
TWI785849B (zh)	2022-12-01	(甲基)丙烯酸酯黏著劑組成物
JP2018100385A (ja)	2018-06-28	アクリル系粘着剤組成物、およびそれを用いてなる粘着剤、粘着シート、ならびに粘着剤層付偏光板
JP2018002910A (ja)	2018-01-11	粘着剤組成物、およびそれを用いてなる粘着剤並びに偏光板用粘着剤
JP2019031660A (ja)	2019-02-28	粘着剤組成物、およびそれを用いてなる粘着剤、偏光板用粘着剤、ならびに画像表示装置