JP2007126559A5 - - Google Patents

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Publication number: JP2007126559A5
Authority: JP; Japan
Prior art keywords: acrylic resin; group; film; structural unit; optical film
Prior art date: 2005-11-04
Legal status (The legal status 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 status listed.): Granted

Application number

JP2005320516A

Other languages

English (en)

Japanese (ja)

Other versions

JP2007126559A (ja

JP5023470B2 (ja

Filing date

2005-11-04

Publication date

2008-12-11

2005-11-04 Application filed filed Critical

2005-11-04 Priority to JP2005320516A priority Critical patent/JP5023470B2/ja

2005-11-04 Priority claimed from JP2005320516A external-priority patent/JP5023470B2/ja

2006-10-25 Priority to TW095139379A priority patent/TWI406898B/zh

2006-10-31 Priority to KR1020060106036A priority patent/KR101288238B1/ko

2006-11-02 Priority to CNA2006101436066A priority patent/CN1958660A/zh

2007-05-24 Publication of JP2007126559A publication Critical patent/JP2007126559A/ja

2008-12-11 Publication of JP2007126559A5 publication Critical patent/JP2007126559A5/ja

2012-09-12 Application granted granted Critical

2012-09-12 Publication of JP5023470B2 publication Critical patent/JP5023470B2/ja

Status Expired - Fee Related legal-status Critical Current

2025-11-04 Anticipated expiration legal-status Critical

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239000004925 Acrylic resin Substances 0.000 claims description 155
229920000178 Acrylic resin Polymers 0.000 claims description 155
230000003287 optical Effects 0.000 claims description 89
239000000178 monomer Substances 0.000 claims description 81
239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 59
239000000853 adhesive Substances 0.000 claims description 49
230000001070 adhesive Effects 0.000 claims description 49
-1 isocyanate compound Chemical class 0.000 claims description 46
239000011521 glass Substances 0.000 claims description 44
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 42
125000000524 functional group Chemical group 0.000 claims description 40
239000000203 mixture Substances 0.000 claims description 37
239000003431 cross linking reagent Substances 0.000 claims description 23
229910000077 silane Inorganic materials 0.000 claims description 12
125000005396 acrylic acid ester group Chemical group 0.000 claims description 11
DVKJHBMWWAPEIU-UHFFFAOYSA-N Toluene diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 10
125000004432 carbon atoms Chemical group C* 0.000 claims description 10
125000004435 hydrogen atoms Chemical group [H]* 0.000 claims description 9
125000003700 epoxy group Chemical group 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 6
125000003710 aryl alkyl group Chemical group 0.000 claims description 6
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
238000010030 laminating Methods 0.000 claims description 6
239000000463 material Substances 0.000 claims description 6
125000003277 amino group Chemical group 0.000 claims description 5
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 5
125000003566 oxetanyl group Chemical group 0.000 claims description 5
229940081735 acetylcellulose Drugs 0.000 claims description 4
125000003172 aldehyde group Chemical group 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
125000003368 amide group Chemical group 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
229920005862 polyol Polymers 0.000 claims description 3
150000003077 polyols Chemical class 0.000 claims description 3
230000001681 protective Effects 0.000 claims description 3
230000000875 corresponding Effects 0.000 claims description 2
239000004971 Cross linker Substances 0.000 claims 1
230000000447 dimerizing Effects 0.000 claims 1
239000000758 substrate Substances 0.000 description 38
239000010410 layer Substances 0.000 description 37
206010040844 Skin exfoliation Diseases 0.000 description 27
238000004519 manufacturing process Methods 0.000 description 26
XEKOWRVHYACXOJ-UHFFFAOYSA-N acetic acid ethyl ester Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
239000004973 liquid crystal related substance Substances 0.000 description 20
238000006116 polymerization reaction Methods 0.000 description 19
241000519995 Stachys sylvatica Species 0.000 description 18
238000005187 foaming Methods 0.000 description 16
230000001629 suppression Effects 0.000 description 14
210000002858 crystal cell Anatomy 0.000 description 13
229910052757 nitrogen Inorganic materials 0.000 description 13
CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 12
125000002723 alicyclic group Chemical group 0.000 description 12
239000003505 polymerization initiator Substances 0.000 description 11
239000000243 solution Substances 0.000 description 11
238000006243 chemical reaction Methods 0.000 description 10
229920001577 copolymer Polymers 0.000 description 10
OZAIFHULBGXAKX-VAWYXSNFSA-N Azobisisobutyronitrile Chemical compound N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 9
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 9
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 8
238000005227 gel permeation chromatography Methods 0.000 description 8
PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
239000004793 Polystyrene Substances 0.000 description 7
125000004122 cyclic group Chemical group 0.000 description 7
125000000623 heterocyclic group Chemical group 0.000 description 7
239000003960 organic solvent Substances 0.000 description 7
229920002223 polystyrene Polymers 0.000 description 7
150000001875 compounds Chemical class 0.000 description 6
238000004132 cross linking Methods 0.000 description 6
238000010528 free radical solution polymerization reaction Methods 0.000 description 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
229920005989 resin Polymers 0.000 description 6
239000011347 resin Substances 0.000 description 6
239000011259 mixed solution Substances 0.000 description 5
239000004372 Polyvinyl alcohol Substances 0.000 description 4
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
239000002585 base Substances 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
229910001873 dinitrogen Inorganic materials 0.000 description 4
239000006260 foam Substances 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
239000003999 initiator Substances 0.000 description 4
PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
229920002451 polyvinyl alcohol Polymers 0.000 description 4
230000035939 shock Effects 0.000 description 4
241000894007 species Species 0.000 description 4
229940113165 trimethylolpropane Drugs 0.000 description 4
IAXXETNIOYFMLW-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) 2-methylprop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C(=C)C)CC1C2(C)C IAXXETNIOYFMLW-UHFFFAOYSA-N 0.000 description 3
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 3
229940119545 Isobornyl methacrylate Drugs 0.000 description 3
PSGCQDPCAWOCSH-BREBYQMCSA-N [(1R,3R,4R)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] prop-2-enoate Chemical compound C1C[C@@]2(C)[C@H](OC(=O)C=C)C[C@@H]1C2(C)C PSGCQDPCAWOCSH-BREBYQMCSA-N 0.000 description 3
HRPVXLWXLXDGHG-UHFFFAOYSA-N acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
NLHHRLWOUZZQLW-UHFFFAOYSA-N acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
239000012298 atmosphere Substances 0.000 description 3
PHYWDUIBNMEJSG-UHFFFAOYSA-M coronene-1-carboxylate Chemical compound C1=C2C(C(=O)[O-])=CC3=CC=C(C=C4)C5=C3C2=C2C3=C5C4=CC=C3C=CC2=C1 PHYWDUIBNMEJSG-UHFFFAOYSA-M 0.000 description 3
OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 3
KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 3
238000009826 distribution Methods 0.000 description 3
239000000975 dye Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
238000002156 mixing Methods 0.000 description 3
229920000515 polycarbonate Polymers 0.000 description 3
239000004417 polycarbonate Substances 0.000 description 3
229920003288 polysulfone Polymers 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 2
ZJKPXJLAUAZTIZ-UHFFFAOYSA-N 1-morpholin-2-ylprop-2-en-1-one Chemical compound C=CC(=O)C1CNCCO1 ZJKPXJLAUAZTIZ-UHFFFAOYSA-N 0.000 description 2
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
MXRGSJAOLKBZLU-UHFFFAOYSA-N 3-ethenylazepan-2-one Chemical compound C=CC1CCCCNC1=O MXRGSJAOLKBZLU-UHFFFAOYSA-N 0.000 description 2
FYYIUODUDSPAJQ-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl 2-methylprop-2-enoate Chemical compound C1C(COC(=O)C(=C)C)CCC2OC21 FYYIUODUDSPAJQ-UHFFFAOYSA-N 0.000 description 2
DPTGFYXXFXSRIR-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl prop-2-enoate Chemical compound C1C(COC(=O)C=C)CCC2OC21 DPTGFYXXFXSRIR-UHFFFAOYSA-N 0.000 description 2
ROOXNKNUYICQNP-UHFFFAOYSA-N Ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
229920002284 Cellulose triacetate Polymers 0.000 description 2
IMNIMPAHZVJRPE-UHFFFAOYSA-N DABCO Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
239000004593 Epoxy Substances 0.000 description 2
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinylpyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
229920001567 Vinyl ester Polymers 0.000 description 2
150000001252 acrylic acid derivatives Chemical class 0.000 description 2
238000007792 addition Methods 0.000 description 2
230000032683 aging Effects 0.000 description 2
239000003513 alkali Substances 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
SOGAXMICEFXMKE-UHFFFAOYSA-N butyl 2-methylprop-2-enoate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
238000001816 cooling Methods 0.000 description 2
150000001925 cycloalkenes Chemical group 0.000 description 2
238000001035 drying Methods 0.000 description 2
239000000428 dust Substances 0.000 description 2
238000010556 emulsion polymerization method Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
235000011187 glycerol Nutrition 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
239000011630 iodine Substances 0.000 description 2
229910052740 iodine Inorganic materials 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
125000005397 methacrylic acid ester group Chemical group 0.000 description 2
238000000034 method Methods 0.000 description 2
229910052759 nickel Inorganic materials 0.000 description 2
239000012299 nitrogen atmosphere Substances 0.000 description 2
YNXCGLKMOXLBOD-UHFFFAOYSA-N oxolan-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CCCO1 YNXCGLKMOXLBOD-UHFFFAOYSA-N 0.000 description 2
125000004430 oxygen atoms Chemical group O* 0.000 description 2
230000002093 peripheral Effects 0.000 description 2
229920001230 polyarylate Polymers 0.000 description 2
229920000647 polyepoxide Polymers 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
229920000139 polyethylene terephthalate Polymers 0.000 description 2
239000005020 polyethylene terephthalate Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
239000004814 polyurethane Substances 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
239000011342 resin composition Substances 0.000 description 2
239000005268 rod-like liquid crystal Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
BLRPTPMANUNPDV-UHFFFAOYSA-N silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
150000004756 silanes Chemical class 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
238000010558 suspension polymerization method Methods 0.000 description 2
CIHOLLKRGTVIJN-UHFFFAOYSA-N tBuOOH Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
APAUNQLFVGBQQW-UHFFFAOYSA-N (1,2,2-trimethylcyclohexyl) 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1(C)CCCCC1(C)C APAUNQLFVGBQQW-UHFFFAOYSA-N 0.000 description 1
CLHPBURJMZXHFZ-UHFFFAOYSA-N (1,2,2-trimethylcyclohexyl) prop-2-enoate Chemical compound CC1(C)CCCCC1(C)OC(=O)C=C CLHPBURJMZXHFZ-UHFFFAOYSA-N 0.000 description 1
LBHPSYROQDMVBS-UHFFFAOYSA-N (1-methylcyclohexyl) 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1(C)CCCCC1 LBHPSYROQDMVBS-UHFFFAOYSA-N 0.000 description 1
XPEMPJFPRCHICU-UHFFFAOYSA-N (1-tert-butylcyclohexyl) prop-2-enoate Chemical compound C=CC(=O)OC1(C(C)(C)C)CCCCC1 XPEMPJFPRCHICU-UHFFFAOYSA-N 0.000 description 1
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-Aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-Dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 description 1
BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
YABQYGQKNQNSBG-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)-3,4,5,6-tetramethylbenzene Chemical compound CC1=C(C)C(C)=C(CN=C=O)C(CN=C=O)=C1C YABQYGQKNQNSBG-UHFFFAOYSA-N 0.000 description 1
ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N 1,2-ethanediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
UQAIMZSFWBGBTN-UHFFFAOYSA-L 1,2-xylene;dicyanate Chemical compound [O-]C#N.[O-]C#N.CC1=CC=CC=C1C UQAIMZSFWBGBTN-UHFFFAOYSA-L 0.000 description 1
RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
FYBFGAFWCBMEDG-UHFFFAOYSA-N 1-[3,5-di(prop-2-enoyl)-1,3,5-triazinan-1-yl]prop-2-en-1-one Chemical compound C=CC(=O)N1CN(C(=O)C=C)CN(C(=O)C=C)C1 FYBFGAFWCBMEDG-UHFFFAOYSA-N 0.000 description 1
LTIKIBFTASQKMM-UHFFFAOYSA-N 1-[bis(4-isocyanatophenyl)methyl]-4-isocyanatobenzene Chemical compound C1=CC(N=C=O)=CC=C1C(C=1C=CC(=CC=1)N=C=O)C1=CC=C(N=C=O)C=C1 LTIKIBFTASQKMM-UHFFFAOYSA-N 0.000 description 1
LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
APQXWKHOGQFGTB-UHFFFAOYSA-N 1-ethenyl-9H-carbazole Chemical compound C12=CC=CC=C2NC2=C1C=CC=C2C=C APQXWKHOGQFGTB-UHFFFAOYSA-N 0.000 description 1
DQJSFBCVEPQRLA-UHFFFAOYSA-N 1-methoxyethyl prop-2-enoate Chemical compound COC(C)OC(=O)C=C DQJSFBCVEPQRLA-UHFFFAOYSA-N 0.000 description 1
GZBSIABKXVPBFY-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)CO GZBSIABKXVPBFY-UHFFFAOYSA-N 0.000 description 1
CYLVUSZHVURAOY-UHFFFAOYSA-N 2,2-dibromoethenylbenzene Chemical compound BrC(Br)=CC1=CC=CC=C1 CYLVUSZHVURAOY-UHFFFAOYSA-N 0.000 description 1
IVIDDMGBRCPGLJ-UHFFFAOYSA-N 2,3-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(CO)COCC1CO1 IVIDDMGBRCPGLJ-UHFFFAOYSA-N 0.000 description 1
KQSMCAVKSJWMSI-UHFFFAOYSA-N 2,4-dimethyl-1-N,1-N,3-N,3-N-tetrakis(oxiran-2-ylmethyl)benzene-1,3-diamine Chemical compound CC1=C(N(CC2OC2)CC2OC2)C(C)=CC=C1N(CC1OC1)CC1CO1 KQSMCAVKSJWMSI-UHFFFAOYSA-N 0.000 description 1
ARGCQEVBJHPOGB-UHFFFAOYSA-N 2,5-Dihydrofuran Chemical compound C1OCC=C1 ARGCQEVBJHPOGB-UHFFFAOYSA-N 0.000 description 1
AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 description 1
DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
CUGZWHZWSVUSBE-UHFFFAOYSA-N 2-(oxiran-2-ylmethoxy)ethanol Chemical compound OCCOCC1CO1 CUGZWHZWSVUSBE-UHFFFAOYSA-N 0.000 description 1
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
OZDGMOYKSFPLSE-UHFFFAOYSA-N 2-Methylazacyclopropane Chemical compound CC1CN1 OZDGMOYKSFPLSE-UHFFFAOYSA-N 0.000 description 1
KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-Vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
VUDVPVOIALASLB-UHFFFAOYSA-N 2-[(2-cyano-1-hydroxypropan-2-yl)diazenyl]-3-hydroxy-2-methylpropanenitrile Chemical compound OCC(C)(C#N)N=NC(C)(CO)C#N VUDVPVOIALASLB-UHFFFAOYSA-N 0.000 description 1
PFHOSZAOXCYAGJ-UHFFFAOYSA-N 2-[(2-cyano-4-methoxy-4-methylpentan-2-yl)diazenyl]-4-methoxy-2,4-dimethylpentanenitrile Chemical compound COC(C)(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)(C)OC PFHOSZAOXCYAGJ-UHFFFAOYSA-N 0.000 description 1
WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 1
SYEWHONLFGZGLK-UHFFFAOYSA-N 2-[1,3-bis(oxiran-2-ylmethoxy)propan-2-yloxymethyl]oxirane Chemical compound C1OC1COCC(OCC1OC1)COCC1CO1 SYEWHONLFGZGLK-UHFFFAOYSA-N 0.000 description 1
AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 1
WTYYGFLRBWMFRY-UHFFFAOYSA-N 2-[6-(oxiran-2-ylmethoxy)hexoxymethyl]oxirane Chemical compound C1OC1COCCCCCCOCC1CO1 WTYYGFLRBWMFRY-UHFFFAOYSA-N 0.000 description 1
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DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
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239000002023 wood Substances 0.000 description 1
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HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
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239000011701 zinc Substances 0.000 description 1
QCWXUUIWCKQGHC-UHFFFAOYSA-N zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
229910052726 zirconium Inorganic materials 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N α-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1

JP2005320516A 2005-11-04 2005-11-04 アクリル樹脂組成物及び粘着剤 Expired - Fee Related JP5023470B2 (ja)

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JP2005320516A JP5023470B2 (ja)	2005-11-04	2005-11-04	アクリル樹脂組成物及び粘着剤
TW095139379A TWI406898B (zh)	2005-11-04	2006-10-25	丙烯酸樹脂組成物及黏著劑
KR1020060106036A KR101288238B1 (ko)	2005-11-04	2006-10-31	아크릴 수지 조성물 및 점착제
CNA2006101436066A CN1958660A (zh)	2005-11-04	2006-11-02	丙烯酸树脂组合物和胶粘剂

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2005
- 2005-11-04 JP JP2005320516A patent/JP5023470B2/ja not_active Expired - Fee Related
2006
- 2006-10-25 TW TW095139379A patent/TWI406898B/zh not_active IP Right Cessation
- 2006-10-31 KR KR1020060106036A patent/KR101288238B1/ko active IP Right Grant
- 2006-11-02 CN CNA2006101436066A patent/CN1958660A/zh active Pending

Publication	Publication Date	Title
JP5023470B2 (ja)	2012-09-12	アクリル樹脂組成物及び粘着剤
JP2007126559A5 (zh)	2008-12-11
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JP2008176173A (ja)	2008-07-31	粘着剤付き光学フィルム及び光学積層体
JP2006113574A (ja)	2006-04-27	光学積層体及びその製造方法
JP2006113575A (ja)	2006-04-27	光学積層体
JP2005239805A (ja)	2005-09-08	アクリル樹脂、該樹脂を含有する粘着剤、及び該粘着剤を積層してなる光学積層体
JP5011798B2 (ja)	2012-08-29	粘着剤
US20040092689A1 (en)	2004-05-13	Acrylic resin, adhesive comprising the resin, and optical laminate comprising the adhesive
US20040152812A1 (en)	2004-08-05	Acrylic resin composition, adhesive comprising the composition, and optical laminate comprising the adhesive
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JP4370888B2 (ja)	2009-11-25	粘着剤付光学フィルム及びそれを用いた光学積層体
JP4507774B2 (ja)	2010-07-21	アクリル樹脂組成物及びその用途
US20050215743A1 (en)	2005-09-29	Acrylic resin