KR101362881B1 - 디스플레이용 광학 점착제 조성물 - Google Patents
디스플레이용 광학 점착제 조성물 Download PDFInfo
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- KR101362881B1 KR101362881B1 KR1020100140047A KR20100140047A KR101362881B1 KR 101362881 B1 KR101362881 B1 KR 101362881B1 KR 1020100140047 A KR1020100140047 A KR 1020100140047A KR 20100140047 A KR20100140047 A KR 20100140047A KR 101362881 B1 KR101362881 B1 KR 101362881B1
- Authority
- KR
- South Korea
- Prior art keywords
- acrylate
- meth
- adhesive composition
- sensitive adhesive
- optical pressure
- Prior art date
- 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.)
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- 239000000203 mixture Substances 0.000 title claims abstract description 79
- 239000000853 adhesive Substances 0.000 title claims description 18
- 230000001070 adhesive effect Effects 0.000 title claims description 18
- 230000003287 optical effect Effects 0.000 claims abstract description 75
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims abstract description 68
- 239000000178 monomer Substances 0.000 claims abstract description 67
- 239000011230 binding agent Substances 0.000 claims abstract description 45
- 238000002834 transmittance Methods 0.000 claims abstract description 15
- 230000009477 glass transition Effects 0.000 claims abstract description 14
- 229920001971 elastomer Polymers 0.000 claims abstract description 13
- 239000005060 rubber Substances 0.000 claims abstract description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 84
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 29
- 229920002554 vinyl polymer Polymers 0.000 claims description 25
- -1 hydroxypropyl Chemical group 0.000 claims description 21
- 239000012760 heat stabilizer Substances 0.000 claims description 13
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 12
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 11
- 230000000475 sunscreen effect Effects 0.000 claims description 11
- 239000000516 sunscreening agent Substances 0.000 claims description 11
- 125000002723 alicyclic group Chemical group 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 229920001195 polyisoprene Polymers 0.000 claims description 9
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 claims description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- 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 claims description 4
- 239000000155 melt Substances 0.000 claims description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 claims description 3
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims description 3
- 229940119545 isobornyl methacrylate Drugs 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims description 2
- VEIOBOXBGYWJIT-UHFFFAOYSA-N cyclohexane;methanol Chemical compound OC.OC.C1CCCCC1 VEIOBOXBGYWJIT-UHFFFAOYSA-N 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000002704 decyl 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])* 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 229920000126 latex Polymers 0.000 claims description 2
- 239000004816 latex Substances 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- 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 claims description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 2
- AZIQALWHRUQPHV-UHFFFAOYSA-N prop-2-eneperoxoic acid Chemical class OOC(=O)C=C AZIQALWHRUQPHV-UHFFFAOYSA-N 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 claims description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 230000000052 comparative effect Effects 0.000 description 13
- 239000000463 material Substances 0.000 description 13
- 239000011521 glass Substances 0.000 description 11
- 238000001723 curing Methods 0.000 description 10
- 230000005484 gravity Effects 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 239000010410 layer Substances 0.000 description 6
- 238000000016 photochemical curing Methods 0.000 description 6
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 4
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 4
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 4
- 239000012965 benzophenone Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 4
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 3
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 3
- 239000002313 adhesive film Substances 0.000 description 3
- 239000011203 carbon fibre reinforced carbon Chemical group 0.000 description 3
- 229920003049 isoprene rubber Polymers 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 150000003377 silicon compounds Chemical class 0.000 description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000003017 thermal stabilizer Substances 0.000 description 2
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 2
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 1
- BEYOMQWTUYTTDL-UHFFFAOYSA-N (4-hydroxy-4-methoxycyclohexa-1,5-dien-1-yl)-phenylmethanone Chemical compound C1=CC(OC)(O)CC=C1C(=O)C1=CC=CC=C1 BEYOMQWTUYTTDL-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- BLCHIKLQYBVYAF-UHFFFAOYSA-N 2,5-dimethylhex-2-enoic acid Chemical compound CC(C)CC=C(C)C(O)=O BLCHIKLQYBVYAF-UHFFFAOYSA-N 0.000 description 1
- IGFDJZRYXGAOKQ-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-ethoxyphenol Chemical compound OC1=CC(OCC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 IGFDJZRYXGAOKQ-UHFFFAOYSA-N 0.000 description 1
- UUINYPIVWRZHAG-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-methoxyphenol Chemical compound OC1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 UUINYPIVWRZHAG-UHFFFAOYSA-N 0.000 description 1
- DSBLSFKNWFKZON-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-propoxyphenol Chemical compound CCCOc1ccc(c(O)c1)-c1nc(nc(n1)-c1ccccc1)-c1ccccc1 DSBLSFKNWFKZON-UHFFFAOYSA-N 0.000 description 1
- LHPPDQUVECZQSW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-ditert-butylphenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=CC=CC3=N2)=C1O LHPPDQUVECZQSW-UHFFFAOYSA-N 0.000 description 1
- IYAZLDLPUNDVAG-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical group CC(C)(C)CC(C)(C)C1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 IYAZLDLPUNDVAG-UHFFFAOYSA-N 0.000 description 1
- KLIZOTJVECGYSJ-UHFFFAOYSA-N 2-[2-[3-(benzotriazol-2-yl)-5-(2-phenylpropan-2-yl)phenyl]propan-2-yl]phenol Chemical compound C=1C(N2N=C3C=CC=CC3=N2)=CC(C(C)(C)C=2C(=CC=CC=2)O)=CC=1C(C)(C)C1=CC=CC=C1 KLIZOTJVECGYSJ-UHFFFAOYSA-N 0.000 description 1
- AAXRSWGYLGOFQP-UHFFFAOYSA-N 2-butoxy-1-(2-butoxyphenyl)ethanone Chemical compound CCCCOCC(=O)C1=CC=CC=C1OCCCC AAXRSWGYLGOFQP-UHFFFAOYSA-N 0.000 description 1
- MRDMGGOYEBRLPD-UHFFFAOYSA-N 2-ethoxy-1-(2-ethoxyphenyl)ethanone Chemical compound CCOCC(=O)C1=CC=CC=C1OCC MRDMGGOYEBRLPD-UHFFFAOYSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- MYISVPVWAQRUTL-UHFFFAOYSA-N 2-methylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC=C3SC2=C1 MYISVPVWAQRUTL-UHFFFAOYSA-N 0.000 description 1
- HAZQZUFYRLFOLC-UHFFFAOYSA-N 2-phenyl-4,6-bis(trichloromethyl)-1,3,5-triazine Chemical compound ClC(Cl)(Cl)C1=NC(C(Cl)(Cl)Cl)=NC(C=2C=CC=CC=2)=N1 HAZQZUFYRLFOLC-UHFFFAOYSA-N 0.000 description 1
- OXYZDRAJMHGSMW-UHFFFAOYSA-N 3-chloropropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCl OXYZDRAJMHGSMW-UHFFFAOYSA-N 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- GCPDCGCMGILXLN-UHFFFAOYSA-N 5-butoxy-2-(4,6-diphenyl-1,3,5-triazin-2-yl)phenol Chemical compound OC1=CC(OCCCC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 GCPDCGCMGILXLN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- VYHBFRJRBHMIQZ-UHFFFAOYSA-N bis[4-(diethylamino)phenyl]methanone Chemical compound C1=CC(N(CC)CC)=CC=C1C(=O)C1=CC=C(N(CC)CC)C=C1 VYHBFRJRBHMIQZ-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 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
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- WHGNXNCOTZPEEK-UHFFFAOYSA-N dimethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](C)(OC)CCCOCC1CO1 WHGNXNCOTZPEEK-UHFFFAOYSA-N 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 1
- MQWFLKHKWJMCEN-UHFFFAOYSA-N n'-[3-[dimethoxy(methyl)silyl]propyl]ethane-1,2-diamine Chemical compound CO[Si](C)(OC)CCCNCCN MQWFLKHKWJMCEN-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- LYXOWKPVTCPORE-UHFFFAOYSA-N phenyl-(4-phenylphenyl)methanone Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 LYXOWKPVTCPORE-UHFFFAOYSA-N 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 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
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-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
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
-
- 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
- C09J133/04—Homopolymers or copolymers of esters
-
- 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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
-
- 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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
-
- 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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
- C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/385—Acrylic 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
- C09J9/00—Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks
-
- 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
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/318—Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of liquid crystal displays
-
- 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
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/302—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being pressure-sensitive, i.e. tacky at temperatures inferior to 30°C
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
실시예 1 | 실시예 2 | 실시예 3 | 실시예 4 | 실시예 5 | 실시예 6 | ||
바인더 | 바인더 1 | 75 | 75 | 55 | - | - | - |
바인더 2 | - | - | - | 75 | 55 | 55 | |
바인더 3 | - | - | - | - | - | - | |
바인더 4 | - | - | - | - | - | - | |
광경화형 단량체 | 단량체 1 | 20 | 10 | 10 | 10 | 10 | 10 |
단량체 2 | - | 5 | 5 | 5 | 5 | 5 | |
단량체 3 | - | 3 | 23 | 3 | 23 | 20 | |
단량체 4 | - | - | - | - | - | 3 | |
광개시제 | 4 | 4 | 4 | 4 | 4 | 4 | |
자외선 차단제 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | |
열안정제 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | |
실란 커플링제 | - | 2 | 2 | 2 | 2 | 2 |
실시예 7 | 비교예 1 | 비교예 2 | 비교예 3 | 비교예 4 | 비교예 5 | ||
바인더 | 바인더 1 | - | - | 40 | 90 | - | - |
바인더 2 | - | - | - | - | 40 | 90 | |
바인더 3 | 75 | - | - | - | - | - | |
바인더 4 | - | 75 | - | - | - | - | |
광경화형 단량체 | 단량체 1 | 20 | 20 | 10 | 2 | 10 | 2 |
단량체 2 | - | - | 5 | 1 | 5 | 1 | |
단량체 3 | - | - | 38 | - | 38 | - | |
단량체 4 | - | - | - | - | - | - | |
광개시제 | 4 | 4 | 4 | 4 | 4 | 4 | |
자외선 차단제 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | |
열안정제 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | |
실란 커플링제 | - | - | 2 | 2 | 2 | 2 |
실시예 1 | 실시예 2 | 실시예 3 | 실시예 4 | 실시예 5 | 실시예 6 | |
경화수축율(%) | 2.14 | 2.22 | 2.87 | 2.34 | 2.98 | 2.32 |
접착력(kgf) | 51 | 55 | 48 | 46 | 47 | 46 |
인장강도(gf/mm2) | 26 | 28 | 32 | 28 | 33 | 28 |
연신율(%) | 260 | 240 | 200 | 240 | 245 | 230 |
굴절률 | 1.51 | 1.51 | 1.50 | 1.51 | 1.50 | 1.51 |
가시광선 투과율(%) | 92.1 | 92.3 | 92.8 | 92.3 | 92.7 | 92.4 |
실시예 7 | 비교예 1 | 비교예 2 | 비교예 3 | 비교예 4 | 비교예 5 | |
경화수축율(%) | 2.22 | 2.21 | 3.67 | 1.32 | 3.88 | 1.42 |
접착력(kgf) | 65 | 66 | 38 | 59 | 38 | 58 |
인장강도(gf/mm2) | 42 | 46 | 41 | 25 | 42 | 26 |
연신율(%) | 220 | 180 | 160 | 180 | 330 | 340 |
굴절률 | 1.51 | 1.45 | 1.45 | 1.54 | 1.45 | 1.54 |
가시광선 투과율(%) | 92.1 | 75.2 | 93.2 | 91.8 | 93.1 | 91.7 |
Claims (23)
- 제1항에 있어서, 상기 유리 전이 온도가 -70℃ ~ -20℃인 것을 특징으로 하는 광학 점착제 조성물.
- 제1항에 있어서, 상기 바인더는 폴리이소프렌 (메타)아크릴레이트 올리고머인 것을 특징으로 하는 광학 점착제 조성물.
- 제3항에 있어서, 상기 폴리이소프렌 (메타)아크릴레이트 올리고머는 비닐기를 갖는 것을 특징으로 하는 광학 점착제 조성물.
- 삭제
- 제1항에 있어서, 상기 바인더는 상기 광학 점착제 조성물 중 50-80중량%로 포함되는 것을 특징으로 하는 광학 점착제 조성물.
- 제1항에 있어서, 상기 광학 점착제 조성물은 상기 바인더, 광경화형 단량체, 광개시제, 자외선 차단제 및 열안정제를 포함하는 광학 점착제 조성물.
- 제7항에 있어서, 상기 광경화형 단량체는 히드록시기를 갖는 비닐계 단량체, 카르복시기를 갖는 비닐계 단량체, 지환족기를 갖는 비닐계 단량체 및 알킬기를 갖는 비닐계 단량체로 이루어진 군으로부터 선택되는 1종 이상인 것을 특징으로 하는 광학 점착제 조성물.
- 제8항에 있어서, 상기 히드록시기를 갖는 비닐계 단량체는 카프로락톤 변성 하이드록시 아크릴레이트, 히드록시에틸 (메타)아크릴레이트, 히드록시프로필 (메타)아크릴레이트, 히드록시부틸 (메타)아크릴레이트, 히드록시펜틸 (메타)아크릴레이트, 히드록시헥실 (메타)아크릴레이트, 1,4-시클로헥산디메탄올 모노 (메타)아크릴레이트, 1-클로로-2-히드록시프로필 (메타)아크릴레이트, 디에틸렌글리콜 모노 (메타)아크릴레이트, 1,6-헥산디올 모노 (메타)아크릴레이트, 펜타에리스리톨 트리 (메타)아크릴레이트, 디펜타에리스리톨 펜타 (메타)아크릴레이트, 네오펜틸 글라이콜 모노 (메타)아크릴레이트, 트리메틸올프로페인 디 (메타)아크릴레이트, 트리메틸올에테인 디 (메타)아크릴레이트, 2-히드록시-3-페닐옥시프로필 (메타)아크릴레이트, 4-히드록시사이클로헥실 (메타)아크릴레이트, 2-히드록시-3-페닐옥시 (메타)아크릴레이트, 4-히드록시사이클로헥실 (메타)아크릴레이트, 및 사이클로헥세인 디메탄올 모노 (메타)아크릴레이트로 이루어진 군으로부터 선택되는 1종 이상인 것을 특징으로 하는 광학 점착제 조성물.
- 제8항에 있어서, 상기 카르복시기를 갖는 비닐계 단량체는 아크릴산, 메타크릴산, 이타콘산, 말레산, 푸마르산 및 비닐 초산으로 이루어진 군으로부터 선택되는 1종 이상인 것을 특징으로 하는 광학 점착제 조성물.
- 제8항에 있어서, 상기 지환족기를 갖는 비닐계 단량체는 이소보르닐 아크릴레이트, 이소보르닐 메타아크릴레이트, 사이클로헥실 (메타)아크릴레이트 및 사이클로펜틸 (메타)아크릴레이트로 이루어진 군으로부터 선택되는 1종 이상인 것을 특징으로 하는 광학 점착제 조성물.
- 제8항에 있어서, 상기 알킬기를 갖는 비닐계 단량체는 메틸 (메타)아크릴레이트, 에틸 (메타)아크릴레이트, 프로필 (메타)아크릴레이트, n-부틸 (메타)아크릴레이트, t-부틸 (메타)아크릴레이트, iso-부틸 (메타)아크릴레이트, 펜틸 (메타)아크릴레이트, 헥실 (메타)아크릴레이트, 헵틸 (메타)아크릴레이트, 옥틸 (메타)아크릴레이트, 노닐 (메타)아크릴레이트, 데실 (메타)아크릴레이트, 도데실 (메타)아크릴레이트 및 라우릴 (메타)아크릴레이트로 이루어진 군으로부터 선택되는 1종 이상인 것을 특징으로 하는 광학 점착제 조성물.
- 제7항에 있어서, 상기 광학 점착제 조성물은 상기 바인더 50-80중량%, 광경화형 단량체 19-40중량%, 광개시제 0.8-8중량%, 자외선 차단제 0.1-1중량% 및 열안정제 0.1-1중량%를 포함하는 것을 특징으로 하는 광학 점착제 조성물.
- 제1항에 있어서, 상기 광학 점착제 조성물은 실란 커플링제를 더 포함하는 것을 특징으로 하는 광학 점착제 조성물.
- 제14항에 있어서, 상기 광학 점착제 조성물은 상기 바인더 50-80중량%, 광경화형 단량체 18-38중량%, 광개시제 0.8-5중량%, 자외선 차단제 0.1-1중량%, 열안정제 0.1-2중량% 및 실란 커플링제 1-5중량%를 포함하는 것을 특징으로 하는 광학 점착제 조성물.
- 제1항에 있어서, 상기 광학 점착제 조성물은 우레탄 아크릴레이트, 폴리에스터 아크릴레이트, 아크릴 아크릴레이트 올리고머으로 이루어진 그룹으로부터 1종 이상 더 포함하는 것을 특징으로 하는 광학 점착제 조성물.
- 제1항에 있어서, 상기 광학 점착제 조성물은 비경화성 러버를 더 포함하는 것을 특징으로 하는 광학 점착제 조성물.
- 제17항에 있어서, 상기 비경화성 러버는 카복실레이트된 러버계, 수소첨가된 러버계, 라텍스계로 이루어진 군으로부터 선택되는 1종 이상인 것을 특징으로 하는 광학 점착제 조성물.
- 제1항에 있어서, 상기 광학 점착제 조성물은 파장 400-800nm에서 가시광선 투과율이 90% 이상인 것을 특징으로 하는 광학 점착제 조성물.
- 제1항에 있어서, 상기 광학 점착제 조성물은 경화 수축율 0 초과 3% 이하인 것을 특징으로 하는 광학 점착제 조성물.
- 제1항에 있어서, 상기 광학 점착제 조성물은 굴절률이 1.46 내지 1.53인 것을 특징으로 하는 광학 점착제 조성물,
- 제1항에 있어서, 상기 바인더는 38℃에서 용융 점도가 30 ~ 190Pa.s인 것을 특징으로 하는 광학 점착제 조성물.
- 제1항 내지 제4항, 제6항 내지 제22항 중 어느 한 항의 광학 점착제 조성물을 판넬의 각 층간의 점착제로 사용한 전자 기기.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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KR1020100140047A KR101362881B1 (ko) | 2010-12-31 | 2010-12-31 | 디스플레이용 광학 점착제 조성물 |
CN2011102939951A CN102533132A (zh) | 2010-12-31 | 2011-09-27 | 用于显示器的光学透明粘合剂和包括该粘合剂的电子装置 |
TW100135254A TWI532802B (zh) | 2010-12-31 | 2011-09-29 | 顯示器用光學透明黏著劑及包含該黏著劑之電子裝置 |
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CN102898959B (zh) * | 2011-07-25 | 2016-07-06 | 汉高股份有限及两合公司 | 一种可光固化的粘合剂组合物及其用途 |
CN103031106A (zh) * | 2013-01-09 | 2013-04-10 | 王胜华 | 一种用于电容式触摸屏粘接的光固化胶粘剂及其制备方法 |
KR101628435B1 (ko) * | 2013-01-21 | 2016-06-08 | 제일모직주식회사 | 점착 필름, 이를 위한 점착제 조성물 및 이를 포함하는 디스플레이 부재 |
CN103184029A (zh) * | 2013-04-18 | 2013-07-03 | 深圳市飞世尔实业有限公司 | 一种用于电容式触摸屏粘接的光固化胶粘剂及其制备方法 |
CN105934450B (zh) * | 2014-06-30 | 2018-06-08 | 株式会社Lg化学 | 可固化组合物 |
KR101932489B1 (ko) * | 2014-07-30 | 2018-12-27 | 주식회사 엘지화학 | 광경화성 점접착제 조성물, 점접착 필름 및 점접착 필름의 제조 방법 |
JP6614833B2 (ja) * | 2015-07-15 | 2019-12-04 | 日東電工株式会社 | 光学積層体の製造方法 |
CN106928870A (zh) * | 2017-02-09 | 2017-07-07 | 河源然生新材料有限公司 | 一种液态光学透明胶及其制作方法 |
TWI782066B (zh) | 2017-08-03 | 2022-11-01 | 德商漢高股份有限及兩合公司 | 可固化的聚矽氧光學透明黏著劑及其用途 |
KR102229464B1 (ko) | 2017-10-20 | 2021-03-18 | 주식회사 엘지화학 | 점착 조성물, 점착 필름 및 이를 포함하는 스마트 윈도우 |
CN108003799A (zh) * | 2017-12-11 | 2018-05-08 | 南京工业职业技术学院 | 一种耐水洗多用途随意贴及其制备方法 |
WO2019133580A1 (en) | 2017-12-27 | 2019-07-04 | Henkel IP & Holding GmbH | Optically clear pressure sensitive adhesives and uses thereof |
CN108467697A (zh) * | 2018-03-13 | 2018-08-31 | 广东固乐邦新材料科技有限公司 | 一种防爆钢化膜贴膜用uv胶 |
KR102214755B1 (ko) * | 2019-04-18 | 2021-02-10 | 주식회사 애스크와이 | 연신성 광학 필름 |
CN115197664B (zh) * | 2022-08-01 | 2023-06-02 | 业成科技(成都)有限公司 | 光学胶组合物、光学胶膜及制造光学胶膜之方法 |
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KR100815383B1 (ko) | 2006-12-28 | 2008-03-20 | 제일모직주식회사 | 점착필름 형성용 광경화성 조성물 및 이를 포함하는 다이싱다이본딩 필름 |
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