TW201908443A - Adhesive tape - Google Patents
Adhesive tapeInfo
- Publication number
- TW201908443A TW201908443A TW107125746A TW107125746A TW201908443A TW 201908443 A TW201908443 A TW 201908443A TW 107125746 A TW107125746 A TW 107125746A TW 107125746 A TW107125746 A TW 107125746A TW 201908443 A TW201908443 A TW 201908443A
- Authority
- TW
- Taiwan
- Prior art keywords
- adhesive tape
- meth
- adhesive
- acrylate
- base material
- Prior art date
Links
- 239000002390 adhesive tape Substances 0.000 title claims abstract description 81
- 239000006260 foam Substances 0.000 claims abstract description 28
- 230000006835 compression Effects 0.000 claims abstract description 27
- 238000007906 compression Methods 0.000 claims abstract description 27
- 239000012790 adhesive layer Substances 0.000 claims abstract description 25
- 239000000463 material Substances 0.000 claims description 34
- 239000000758 substrate Substances 0.000 claims description 34
- 238000006073 displacement reaction Methods 0.000 claims description 19
- 238000005259 measurement Methods 0.000 claims description 8
- 229920005672 polyolefin resin Polymers 0.000 claims description 8
- 239000011342 resin composition Substances 0.000 claims description 6
- 238000003860 storage Methods 0.000 claims description 6
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 5
- 238000012423 maintenance Methods 0.000 claims description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 5
- 239000011229 interlayer Substances 0.000 claims description 4
- 239000004840 adhesive resin Substances 0.000 claims description 2
- 229920006223 adhesive resin Polymers 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 238000003825 pressing Methods 0.000 abstract description 14
- 238000000034 method Methods 0.000 abstract description 8
- 230000007423 decrease Effects 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 38
- 239000000178 monomer Substances 0.000 description 26
- -1 polyethylene Polymers 0.000 description 19
- 230000000052 comparative effect Effects 0.000 description 16
- 239000000853 adhesive Substances 0.000 description 13
- 230000001070 adhesive effect Effects 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- 238000005452 bending Methods 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 8
- 229920000058 polyacrylate Polymers 0.000 description 8
- 229920000573 polyethylene Polymers 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 238000004132 cross linking Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 239000003522 acrylic cement Substances 0.000 description 4
- 229920006243 acrylic copolymer Polymers 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 238000013461 design Methods 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 239000006087 Silane Coupling Agent Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- OZFIGURLAJSLIR-UHFFFAOYSA-N 1-ethenyl-2h-pyridine Chemical compound C=CN1CC=CC=C1 OZFIGURLAJSLIR-UHFFFAOYSA-N 0.000 description 2
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-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
- 238000001035 drying Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
- LNKDTZRRFHHCCV-UHFFFAOYSA-N 1-ethenyl-2h-pyrimidine Chemical compound C=CN1CN=CC=C1 LNKDTZRRFHHCCV-UHFFFAOYSA-N 0.000 description 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
- PBGPBHYPCGDFEZ-UHFFFAOYSA-N 1-ethenylpiperidin-2-one Chemical compound C=CN1CCCCC1=O PBGPBHYPCGDFEZ-UHFFFAOYSA-N 0.000 description 1
- CTXUTPWZJZHRJC-UHFFFAOYSA-N 1-ethenylpyrrole Chemical compound C=CN1C=CC=C1 CTXUTPWZJZHRJC-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-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
- FWLHAQYOFMQTHQ-UHFFFAOYSA-N 2-N-[8-[[8-(4-aminoanilino)-10-phenylphenazin-10-ium-2-yl]amino]-10-phenylphenazin-10-ium-2-yl]-8-N,10-diphenylphenazin-10-ium-2,8-diamine hydroxy-oxido-dioxochromium Chemical compound O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.Nc1ccc(Nc2ccc3nc4ccc(Nc5ccc6nc7ccc(Nc8ccc9nc%10ccc(Nc%11ccccc%11)cc%10[n+](-c%10ccccc%10)c9c8)cc7[n+](-c7ccccc7)c6c5)cc4[n+](-c4ccccc4)c3c2)cc1 FWLHAQYOFMQTHQ-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- ZEUKUBHCGFPLKU-UHFFFAOYSA-N C(=O)(C=C)C1=C2NC(=C1)C=C1C=CC(=N1)C=C1C=CC(N1)=CC=1C=CC(N1)=C2 Chemical compound C(=O)(C=C)C1=C2NC(=C1)C=C1C=CC(=N1)C=C1C=CC(N1)=CC=1C=CC(N1)=C2 ZEUKUBHCGFPLKU-UHFFFAOYSA-N 0.000 description 1
- WQPNQZGZGLEVIK-UHFFFAOYSA-N C(C)(C)C=1C(NC(C1)=N)=N Chemical compound C(C)(C)C=1C(NC(C1)=N)=N WQPNQZGZGLEVIK-UHFFFAOYSA-N 0.000 description 1
- FQDPWVYMHQKEMP-UHFFFAOYSA-N C1(CCCCC1)C=1C(NC(C1)=N)=N Chemical compound C1(CCCCC1)C=1C(NC(C1)=N)=N FQDPWVYMHQKEMP-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- IAKYHJCZXYJUJC-UHFFFAOYSA-N P(=O)(OCCO)(OC=CC)OC(C)=O Chemical compound P(=O)(OCCO)(OC=CC)OC(C)=O IAKYHJCZXYJUJC-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000826860 Trapezium Species 0.000 description 1
- VEPKQEUBKLEPRA-UHFFFAOYSA-N VX-745 Chemical compound FC1=CC(F)=CC=C1SC1=NN2C=NC(=O)C(C=3C(=CC=CC=3Cl)Cl)=C2C=C1 VEPKQEUBKLEPRA-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000001204 arachidyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 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 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 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 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 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 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- LDHQCZJRKDOVOX-IHWYPQMZSA-N isocrotonic acid Chemical compound C\C=C/C(O)=O LDHQCZJRKDOVOX-IHWYPQMZSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000001421 myristyl 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])[H] 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910021392 nanocarbon Inorganic materials 0.000 description 1
- 125000001196 nonadecyl 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])C([H])([H])[H] 0.000 description 1
- MDYPDLBFDATSCF-UHFFFAOYSA-N nonyl prop-2-enoate Chemical compound CCCCCCCCCOC(=O)C=C MDYPDLBFDATSCF-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002958 pentadecyl 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])[H] 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- JXRQWZOCXXIAIA-UHFFFAOYSA-N prop-2-enenitrile cyanide Chemical compound C(C=C)#N.[C-]#N JXRQWZOCXXIAIA-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 125000002889 tridecyl 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])[H] 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
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical group [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- 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
- C09J7/24—Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/241—Polyolefin, e.g.rubber
-
- 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
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- 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
- C09J201/00—Adhesives based on unspecified macromolecular compounds
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- 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
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- 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
- C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
- C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
- C09J2301/122—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present only on one side of the carrier, e.g. single-sided adhesive tape
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- 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
- C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
- C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
- C09J2301/124—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present on both sides of the carrier, e.g. double-sided adhesive tape
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- 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
- C09J2301/312—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 parameters being the characterizing feature
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
本發明係關於加壓況時的厚度尺寸安定性優異,適用於例如智慧手機、平板終端機等電子機器、車用顯示機、TV等構造接著用途的黏著帶。 The present invention relates to an adhesive tape excellent in thickness dimension stability under pressurized conditions, and suitable for use in electronic devices such as smartphones, tablet terminals, car display devices, and TVs.
智慧手機、平板終端機等攜帶式電子機器,一般採行由觸控板、與收容液晶模組之框體的組合構造。而且,例如為了將觸控板與框體固定,使用黏著帶。又,其亦使用於為了將車用顯示機、TV液晶顯示器(LCD)面板及有機EL面板、與框體固定。 Portable electronic devices such as smart phones and tablet terminals generally adopt a combination structure composed of a touch panel and a frame housing a liquid crystal module. Moreover, for example, in order to fix the touchpad to the frame, an adhesive tape is used. In addition, it is also used to fix a vehicle display, a TV liquid crystal display (LCD) panel, and an organic EL panel to a housing.
近年來,該等電子機器正朝薄型化、小型化演進。隨此進展,例如FPC(Flexible Printed Circuits,撓性印刷電路)在機器內部被彎曲呈更尖銳的銳角,導致成為時常被施加強反彈力的內部構造。又,為了更增加LCD顯示區域,圍繞液晶面板的框(邊框)寬度變窄、亦即演進為窄邊框化。所以,將框體與前面板固定的黏著帶亦必需窄幅化。但為了承受來自內部的FPC等反彈力、以及來自外部的衝擊,不僅需求黏著劑層的接著強度,亦必需要求基材的強度。 In recent years, these electronic devices are evolving toward thinness and miniaturization. With this development, for example, FPC (Flexible Printed Circuits) is bent inside the machine at a sharper acute angle, resulting in an internal structure to which a strong rebound force is often applied. In addition, in order to increase the LCD display area, the width of the frame (frame) surrounding the liquid crystal panel becomes narrower, that is, the frame becomes narrower. Therefore, the adhesive tape that fixes the frame and the front panel must also be narrowed. However, in order to withstand the rebound force from the internal FPC and the impact from the outside, not only the adhesion strength of the adhesive layer but also the strength of the substrate must be required.
將窄幅黏著帶黏貼於框體時,一般採行利用壓合機實施加壓步驟。此時,對黏著帶施加的壓力係涵括0.1MPa~5.0MPa的廣範圍。而且,當黏著帶在該壓力範圍內的厚度變化較大時,如 圖4(A)所示,有因雙面黏著帶41的尺寸變化,導致在蓋板42與框體43間生成間隙G,而降低一體感,大幅損及原本的外觀的情形。又,當因壓力變動所造成之雙面黏著帶41的厚度變化差較大時,頗難預測間隙G而設計蓋板42與框體43,增加設計困難度。又,於加壓步驟後,隨時間經過,雙面黏著帶41的尺寸復原時,如圖4(B)所示,有蓋板42從框體43蹦出,當墜落時造成蓋板42遭破損的可能性。 When the narrow-width adhesive tape is adhered to the frame, a pressing machine is generally used to perform the pressing step. At this time, the pressure applied to the adhesive tape covers a wide range of 0.1 MPa to 5.0 MPa. Moreover, when the thickness of the adhesive tape varies greatly within this pressure range, as shown in FIG. 4 (A), there is a gap G between the cover 42 and the frame 43 due to the size change of the double-sided adhesive tape 41 , And reduce the sense of unity, greatly damaging the original appearance of the situation. In addition, when the difference in thickness of the double-sided adhesive tape 41 due to pressure fluctuation is large, it is quite difficult to predict the gap G and design the cover 42 and the frame 43 to increase the difficulty of design. In addition, after the pressing step, as time passes, when the size of the double-sided adhesive tape 41 is restored, as shown in FIG. 4 (B), a cover 42 pops out of the frame 43, causing the cover 42 to suffer when dropped The possibility of damage.
但是,此種黏著帶的基材一般係使用例如:以聚乙烯為主成分的聚烯烴系發泡體、於丙烯酸樹脂中添加了各種填料的壓克力泡棉。例如專利文獻1所記載的雙面黏著帶,係在發泡體基材的雙面上設計丙烯酸系黏著劑層。而且,該發泡體基材之具體例記載有聚乙烯發泡體、聚丙烯發泡體等聚烯烴系樹脂發泡體。該發泡體基材的厚度係50~150μm、30%壓縮荷重係5~200kPa。 However, the base material of such an adhesive tape generally uses, for example, a polyolefin-based foam containing polyethylene as a main component, and acrylic foam to which various fillers are added to acrylic resin. For example, in the double-sided adhesive tape described in Patent Document 1, an acrylic adhesive layer is designed on both sides of the foam base material. Furthermore, specific examples of the foam base material include polyolefin resin foams such as polyethylene foams and polypropylene foams. The thickness of the foam base material is 50 to 150 μm, and the 30% compression load is 5 to 200 kPa.
專利文獻2所記載的防水用雙面黏著帶,目的在於行動電子機器的零件固定,由聚烯烴系發泡體基材與黏著劑層所構成。而且,該聚烯烴系發泡體基材的厚度係70~300μm、25%壓縮強度係40~160kPa、拉伸強度係300~1500N/cm2、厚度方向平均氣泡徑係1~100μm、流動方向與寬度方向的平均氣泡徑係1.2~700μm。 The waterproof double-sided adhesive tape described in Patent Document 2 is intended to fix components of a mobile electronic device, and is composed of a polyolefin-based foam base material and an adhesive layer. Moreover, the thickness of the polyolefin-based foam substrate is 70 to 300 μm, the 25% compressive strength is 40 to 160 kPa, the tensile strength is 300 to 1500 N / cm 2 , the average bubble diameter in the thickness direction is 1 to 100 μm, and the flow direction The average bubble diameter in the width direction is 1.2 to 700 μm.
專利文獻3所記載的黏著帶,係在發泡體基材至少一面上設有黏著劑層。而且,發泡體基材的具體例記載有聚乙烯、聚丙烯等聚烯烴系發泡體基材。該發泡體基材的厚度在300μm以下、層間強度係6~50N/cm、25%壓縮強度係30kPa以上、拉伸強度係300N/cm2以上、厚度方向平均氣泡徑係10~100μm、流動方向與寬度方向的平均氣泡徑係10~700μm。 The adhesive tape described in Patent Document 3 is provided with an adhesive layer on at least one surface of the foam base material. Furthermore, specific examples of the foam base material include polyolefin-based foam base materials such as polyethylene and polypropylene. The thickness of the foam substrate is 300 μm or less, the interlayer strength system is 6 to 50 N / cm, the 25% compression strength system is 30 kPa or more, the tensile strength system is 300 N / cm 2 or more, and the thickness average bubble diameter system is 10 to 100 μm. The average bubble diameter in the direction and width direction is 10 to 700 μm.
專利文獻4所記載的交聯聚烯烴系樹脂發泡片,係具有較高的衝擊吸收性與抗靜電性。該發泡片的發泡倍率係1.1~2.8cm3/g、氣泡MD的平均氣泡徑係150~250μm、CD的平均氣泡徑係120~300μm、厚度係0.02~1.9mm、25%壓縮強度係250~1500kPa。 The crosslinked polyolefin resin foam sheet described in Patent Document 4 has high impact absorption and antistatic properties. The expansion ratio of the foamed sheet is 1.1 to 2.8 cm 3 / g, the average bubble diameter of the bubble MD is 150 to 250 μm, the average bubble diameter of the CD is 120 to 300 μm, the thickness is 0.02 to 1.9 mm, and the 25% compression strength system 250 ~ 1500kPa.
專利文獻5所記載的黏著片,係因窄幅化造成的性能降低較少。該黏著片的100%模數M[N/mm2基材]與發泡體密度D[g/cm3]的關係為9.0≦(M/D),100%模數M較高於4.0[N/mm2基材]。 The adhesive sheet described in Patent Document 5 has less performance degradation due to narrowing. The relationship between the 100% modulus M [N / mm 2 substrate] of the adhesive sheet and the foam density D [g / cm 3 ] is 9.0 ≦ (M / D), and the 100% modulus M is higher than 4.0 [ N / mm 2 substrate].
專利文獻6記載有:用於將行動電子機器的顯示部或顯示部保護材固定於框體的固定構件(具發泡體基材的黏著帶)。該固定構件的窄幅部平均寬度W[mm]、固定構件的100%模數M[N/mm2基材]、及發泡體基材厚度Hs[mm],係滿足0.4/(M×Hs)≦W式。 Patent Document 6 describes a fixing member (adhesive tape with a foam base material) for fixing a display part or a display part protective material of a mobile electronic device to a housing. The average width W [mm] of the narrow part of the fixing member, the 100% modulus M [N / mm 2 base material] of the fixing member, and the thickness Hs [mm] of the foam base material satisfy 0.4 / (M × Hs) ≦ W type.
但是,專利文獻1~6中,相關因利用壓合機施行加壓步驟而造成的帶厚度變化、與經壓合步驟後的帶厚度之維持率,並未充分檢討。又,根據本發明人等的發現,專利文獻1~4所記載的習知物性評價法,針對該基材是否適合於窄幅黏著帶並無充分評價。例如專利文獻1~4所記載「壓縮強度」或「壓縮荷重」,只不過為厚度方向的硬度指標,並非壓縮後的厚度變化指標。專利文獻2與3所記載的「拉伸強度」、「拉伸強度」或「層間強度」,僅為基材破壞時的強度。專利文獻3與4所記載的「平均氣泡徑」或「發泡倍率」,只不過為表示發泡程度的指標。專利文獻5所記載「100%模數」僅表示帶的拉伸強度。專利文獻6所記載之式「0.4/(M×Hs) ≦W」僅為拉伸強度、與帶厚度及帶寬度的關係式。 However, in Patent Documents 1 to 6, the belt thickness variation due to the pressurization step performed by the laminator and the maintenance ratio of the belt thickness after the lamination step have not been fully reviewed. In addition, according to the findings of the present inventors, the conventional physical property evaluation methods described in Patent Documents 1 to 4 do not fully evaluate whether the substrate is suitable for a narrow adhesive tape. For example, the "compressive strength" or "compressive load" described in Patent Documents 1 to 4 are merely an index of hardness in the thickness direction, not an index of thickness change after compression. The "tensile strength", "tensile strength", or "interlayer strength" described in Patent Documents 2 and 3 are only the strengths at the time of base material failure. The "average bubble diameter" or "expansion ratio" described in Patent Documents 3 and 4 are merely indicators of the degree of expansion. The “100% modulus” described in Patent Document 5 represents only the tensile strength of the belt. The expression “0.4 / (M × Hs) ≦ W” described in Patent Document 6 is only a relational expression of tensile strength, tape thickness and tape width.
即,專利文獻1~6所記載習知之物性評價法,尤其對於極窄幅黏著帶未必能直接應用。另一方面,根據本發明人等的發現,使用極窄幅黏著帶,利用壓合機將蓋板與框體施行加壓的步驟時,加壓後的壓縮變形率成為重要因素,又,在加壓後經時變形率的維持率、玻璃蓋與框體不易剝落方面,荷重-位移曲線中的高荷重與低位移亦屬重要因素。 That is, the conventional physical property evaluation methods described in Patent Documents 1 to 6 may not be directly applicable particularly to very narrow adhesive tapes. On the other hand, according to the findings of the present inventors, when a very narrow adhesive tape is used and the cover plate and the frame are subjected to a pressurization step using a laminator, the compression deformation rate after pressurization becomes an important factor. In terms of the maintenance rate of the deformation rate over time after pressing, and the glass cover and the frame body are not easy to peel off, the high load and low displacement in the load-displacement curve are also important factors.
專利文獻1:日本專利第5947870號公報 Patent Document 1: Japanese Patent No. 5947870
專利文獻2:日本專利第4623198號公報 Patent Document 2: Japanese Patent No. 4623198
專利文獻3:日本專利第5517015號公報 Patent Document 3: Japanese Patent No. 5517015
專利文獻4:國際公開第2015/046526號 Patent Literature 4: International Publication No. 2015/046526
專利文獻5:日本專利特開2017-2292公報 Patent Literature 5: Japanese Patent Laid-Open Publication No. 2017-2292
專利文獻6:日本專利特開2017-2293公報 Patent Literature 6: Japanese Patent Laid-Open Publication No. 2017-2293
本發明係為了解決如上述習知技術課題而完成者。即,本發明目的在於提供一種黏著帶,其較佳係極窄幅黏著帶,厚度尺寸安定性優異,例如在將蓋板與框體進行壓合的步驟等加壓步驟中所產生的間隙G小,不易因間隙G而損及製品外觀,且製品墜落時不易因間隙G而發生破損。 The present invention has been completed to solve the aforementioned conventional technical problems. That is, an object of the present invention is to provide an adhesive tape, which is preferably a very narrow adhesive tape, and has excellent thickness stability, such as the gap G generated during the pressing step such as the step of pressing the cover plate and the frame body Small, it is not easy to damage the appearance of the product due to the gap G, and the product is not likely to be damaged due to the gap G when the product falls.
本發明者等為了達成上述目的經深入鑽研,結果發現使用特定物性的基材係屬非常有效,遂完成本發明。 The inventors of the present invention have intensively studied in order to achieve the above object, and as a result, it has been found that the use of a substrate with specific physical properties is very effective, and the present invention has been completed.
即,本發明的黏著帶,係在基材的單面或雙面上設有黏著劑層的黏著帶,其特徵為,上述基材係發泡體,在依0.3~5.0MPa範圍內經壓縮時之接著時的壓縮變形率係0~-10%。 That is, the adhesive tape of the present invention is an adhesive tape provided with an adhesive layer on one side or both sides of the base material, and is characterized in that the base material-based foam is compressed within the range of 0.3 to 5.0 MPa The compression deformation rate at the time of follow-up is 0 ~ -10%.
在前述用途中,一般使用含有獨立氣泡的聚乙烯系發泡基材。若將高壓縮強度發泡基材與低壓縮強度發泡基材進行比較,則低壓縮強度發泡基材因壓力產生的變形較大。又,即使為高壓縮強度發泡基材,若依0.1~5.0MPa的非常高壓力施行加壓,仍因塑性變形導致由原本厚度發生較大變化。另一方面,本發明的黏著帶係厚度尺寸安定性優異,例如在將蓋板與框體施行壓合的步驟等加壓步驟中產生的間隙G小,不易因間隙G造成損及製品外觀,且製品墜落時不易因間隙G而發生破損。所以,在需要此種特性的領域中能有效使用於各種用途。 In the aforementioned applications, a polyethylene-based foamed substrate containing independent bubbles is generally used. If the high-compressive-strength foamed base material is compared with the low-compressive-strength foamed base material, the deformation of the low-compressive-strength foamed base material due to pressure is large. In addition, even if it is a high-compressive-strength foamed base material, if it is pressurized at a very high pressure of 0.1 to 5.0 MPa, the original thickness still changes greatly due to plastic deformation. On the other hand, the adhesive tape of the present invention is excellent in thickness dimension stability. For example, the gap G generated during the pressing step such as the step of pressing the cover plate and the frame is small, and it is not easy to damage the appearance of the product due to the gap G. Moreover, when the product falls, it is not easy to be damaged due to the gap G. Therefore, it can be effectively used for various applications in fields where such characteristics are required.
11‧‧‧基材(或雙面黏著帶) 11‧‧‧ Base material (or double-sided adhesive tape)
12‧‧‧端子 12‧‧‧terminal
31‧‧‧雙面黏著帶 31‧‧‧ Double-sided adhesive tape
32‧‧‧SUS304製T字夾具 32‧‧‧SUS304 T-shaped fixture
33‧‧‧玻璃板 33‧‧‧glass plate
41‧‧‧雙面黏著帶 41‧‧‧ Double-sided adhesive tape
42‧‧‧蓋板 42‧‧‧Cover
43‧‧‧框體 43‧‧‧Frame
G‧‧‧間隙 G‧‧‧Gap
圖1係用於說明實施例之彎曲力矩測定方法的示意剖視圖。 FIG. 1 is a schematic cross-sectional view for explaining the bending moment measuring method of the embodiment.
圖2係用於說明實施例之由動態黏彈性測定所獲得之主曲線的圖。 FIG. 2 is a diagram for explaining the main curve obtained by dynamic viscoelasticity measurement of the embodiment.
圖3係用於說明實施例之荷重-位移曲線測定方法的示意剖視圖。 FIG. 3 is a schematic cross-sectional view for explaining the load-displacement curve measurement method of the embodiment.
圖4(A)及(B)係用於說明習知技術中,在蓋板與框體間發生間隙之問題的示意剖視圖。 4 (A) and (B) are schematic cross-sectional views for explaining the problem of the gap between the cover and the frame in the conventional technology.
本發明所使用基材係只要具有該基材的黏著帶,在依0.3~5.0MPa範圍內施行壓縮時,接著時壓縮變形率成為0~-10%的基材便可,其種類並無限定。例如較佳係含有乙烯-醋酸乙烯酯共聚合體達30質量%以上,且基材的拉伸彈性模數達30N/mm2以上之基材。 The substrate used in the present invention may be any substrate as long as it has an adhesive tape of the substrate and is compressed within the range of 0.3 to 5.0 MPa, and the compression deformation rate becomes 0 to -10% in the following, and the type is not limited. . For example, a substrate containing an ethylene-vinyl acetate copolymer of 30% by mass or more and having a tensile modulus of elasticity of 30 N / mm 2 or more is preferable.
基材較佳係由含有乙烯-醋酸乙烯酯共聚合體與其他聚烯烴系樹脂的聚烯烴系樹脂組成物所構成。其他聚烯烴系樹脂係可舉例如:聚乙烯系樹脂、聚丙烯系樹脂、或該等的混合物。特佳係直鏈低密度聚乙烯(LLDPE)、乙烯丙烯橡膠(EPDM)。 The base material is preferably composed of a polyolefin-based resin composition containing an ethylene-vinyl acetate copolymer and other polyolefin-based resins. Examples of other polyolefin resins include polyethylene resins, polypropylene resins, and mixtures thereof. Extra-fine linear low-density polyethylene (LLDPE) and ethylene propylene rubber (EPDM).
構成基材的樹脂組成物係可利用公知方法製造。例如對含有乙烯-醋酸乙烯酯共聚合體30質量%以上、與其他聚烯烴系樹脂的樹脂組成物照射電子束使其進行交聯,可獲得構成基材的樹脂組成物。可在該交聯之同時或不同時間進行發泡。 The resin composition system constituting the base material can be produced by a known method. For example, a resin composition containing 30% by mass or more of an ethylene-vinyl acetate copolymer and other polyolefin-based resin is irradiated with an electron beam and crosslinked, and a resin composition constituting a base material can be obtained. Foaming can be performed at the same time or at different times during the crosslinking.
構成基材的樹脂組成物,係在不致損及本發明效果之範圍內,亦可含有其他添加劑。具體例係可舉例如:增量劑、交聯劑、抗氧化劑、安定劑、彈性體、偶合劑。又,亦可含有遮光性填料、顏料。遮光性填料具體例係可舉例如:碳黑、奈米碳管、黑色無機填料。顏料具體例係可舉例如:碳黑、苯胺黑、乙炔黑、石墨化碳黑。 The resin composition constituting the base material may be within the range that does not damage the effects of the present invention, and may contain other additives. Specific examples include, for example, extenders, crosslinking agents, antioxidants, stabilizers, elastomers, and coupling agents. Furthermore, it may contain a light-shielding filler and a pigment. Specific examples of the light-shielding filler include carbon black, nano carbon tube, and black inorganic filler. Specific examples of the pigment include carbon black, aniline black, acetylene black, and graphitized carbon black.
基材寬度較佳係0.4~2.0mm、更佳係0.45~1.5mm、特佳係0.6~1.2mm。基材厚度較佳係0.05mm~1.0mm、更佳係 0.05~0.4mm。 The width of the substrate is preferably 0.4 to 2.0 mm, more preferably 0.45 to 1.5 mm, and particularly preferably 0.6 to 1.2 mm. The thickness of the substrate is preferably 0.05 mm to 1.0 mm, and more preferably 0.05 to 0.4 mm.
基材係屬於發泡體,發泡倍率較佳係1.1~3.5倍、更佳係1.5~3.0倍。發泡體的氣泡形狀較佳係球狀。又,從防水性等特性觀點而言,基材較佳係含有獨立氣泡。本發明中,較佳係依基材中所含孔隙徑排除0.3mm~2.0mm尺寸的方式進行管理之基材,更佳係依排除0.4mm~1.4mm尺寸進行管理之基材。又,較佳係未含有與所管理氣泡徑明顯不同尺寸之孔隙(不良氣泡)的基材。 The base material is a foam, and the foaming ratio is preferably 1.1 to 3.5 times and more preferably 1.5 to 3.0 times. The bubble shape of the foam is preferably spherical. In addition, from the viewpoint of characteristics such as water resistance, the base material preferably contains independent bubbles. In the present invention, it is preferable that the substrate is managed in such a manner that the pore diameter contained in the substrate is excluded from the size of 0.3 mm to 2.0 mm, and it is more preferred that the substrate is managed in the manner of excluding 0.4 mm to 1.4 mm. In addition, it is preferably a substrate that does not contain pores (bad bubbles) having a size significantly different from the bubble diameter being managed.
本發明所使用黏著劑層並無特別的限定。構成黏著劑層的黏著劑組成物係可使用例如丙烯酸系、橡膠系、聚矽氧系、胺基甲酸乙酯系等公知各種黏著劑組成物。其中,從耐熱性、耐碰撞性、接著力、防水性的觀點而言,較佳係丙烯酸系黏著劑組成物,而黏著劑層較佳係含有(甲基)丙烯酸酯共聚合體。 The adhesive layer used in the present invention is not particularly limited. As the adhesive composition system that constitutes the adhesive layer, various known adhesive compositions such as acrylic system, rubber system, polysiloxane system, and urethane system can be used. Among them, from the viewpoint of heat resistance, impact resistance, adhesion, and water resistance, an acrylic adhesive composition is preferable, and the adhesive layer preferably contains a (meth) acrylate copolymer.
丙烯酸系黏著劑組成物的構成成分並無特別的限定。丙烯酸系黏著劑組成物通常係含有以具直鏈或分支鏈狀烷基的(甲基)丙烯酸烷基酯為單體主成分而獲得的丙烯酸系聚合物。(甲基)丙烯酸烷基酯具體例係可舉例如:(甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸丙酯、(甲基)丙烯酸異丙酯、(甲基)丙烯酸丁酯、(甲基)丙烯酸異丁酯、(甲基)丙烯酸第二丁酯、(甲基)丙烯酸第三丁酯、(甲基)丙烯酸戊酯、(甲基)丙烯酸異戊酯、(甲基)丙烯酸己酯、(甲基)丙烯酸庚酯、(甲基)丙烯酸辛酯、(甲基)丙烯酸-2-乙基己酯、(甲基)丙烯酸異辛酯、(甲基)丙烯酸壬酯、(甲基)丙烯酸異壬酯、(甲基)丙烯酸癸酯、(甲基)丙烯酸異癸酯、(甲基)丙烯酸十一烷 基酯、(甲基)丙烯酸十二烷基酯、(甲基)丙烯酸十三烷基酯、(甲基)丙烯酸十四烷基酯、(甲基)丙烯酸十五烷基酯、(甲基)丙烯酸十六烷基酯、(甲基)丙烯酸十七烷基酯、(甲基)丙烯酸十八烷基酯、(甲基)丙烯酸十九烷基酯、(甲基)丙烯酸廿烷基酯等(甲基)丙烯酸C1-20烷基酯。其中,較佳係(甲基)丙烯酸C2-14烷基酯、更佳係(甲基)丙烯酸C2-10烷基酯。 The constituent components of the acrylic adhesive composition are not particularly limited. The acrylic adhesive composition generally contains an acrylic polymer obtained by using a (meth) acrylic acid alkyl ester having a linear or branched alkyl group as a main component of a monomer. Specific examples of alkyl (meth) acrylates include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, isopropyl (meth) acrylate, (meth) Group) butyl acrylate, isobutyl (meth) acrylate, second butyl (meth) acrylate, third butyl (meth) acrylate, amyl (meth) acrylate, isoamyl (meth) acrylate Ester, hexyl (meth) acrylate, heptyl (meth) acrylate, octyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, isooctyl (meth) acrylate, (A (Yl) nonyl acrylate, isononyl (meth) acrylate, decyl (meth) acrylate, isodecyl (meth) acrylate, undecyl (meth) acrylate, dodecyl (meth) acrylate Alkyl esters, tridecyl (meth) acrylate, myristyl (meth) acrylate, pentadecyl (meth) acrylate, cetyl (meth) acrylate, (meth) (C) Hexadecyl acrylate, octadecyl (meth) acrylate, nonadecyl (meth) acrylate, eicosyl (meth) acrylate, etc.基 ester. Among them, preferred is C2-14 alkyl (meth) acrylate, and more preferred is C2-10 alkyl (meth) acrylate.
構成丙烯酸系聚合物的單體較佳係適當量使用丙烯酸甲酯等(甲基)丙烯酸C1-3烷基酯。該(甲基)丙烯酸C1-3烷基酯能提升窄邊框接著性、耐荷重性、加工性、窄邊框耐濕熱荷重性。在丙烯酸系聚合物100質量%中,(甲基)丙烯酸C1-3烷基酯的量較佳係2質量%以上、更佳係3~15質量%。該範圍的下限值係從窄邊框接著性、耐荷重性、加工性、窄邊框耐濕熱荷重性的觀點而言具有意義。又,上限值係從實施各種評價時的黏著帶初期黏貼性而言具有意義。 The monomer constituting the acrylic polymer preferably uses C1-3 alkyl (meth) acrylate such as methyl acrylate in an appropriate amount. The C1-3 alkyl (meth) acrylate can improve the adhesiveness of the narrow frame, load resistance, processability, and humidity and heat load resistance of the narrow frame. The amount of C1-3 alkyl (meth) acrylate in 100% by mass of the acrylic polymer is preferably 2% by mass or more, and more preferably 3 to 15% by mass. The lower limit value of this range is meaningful from the viewpoints of narrow frame adhesion, load resistance, workability, and narrow frame heat and moisture load resistance. In addition, the upper limit value is meaningful in terms of the initial adhesiveness of the adhesive tape when various evaluations are performed.
構成丙烯酸系聚合物的單體,為求接著力提升或凝聚力提升,亦可使用含極性基單體、多官能性單體等各種共聚合性單體。亦可組合使用2種以上的共聚合性單體。又,亦可摻合由與含極性基單體或多官能基性單體進行反應所獲得的交聯劑,而形成交聯構造。又,亦可摻合矽烷偶合劑、抗氧化劑等添加劑。 For the monomer constituting the acrylic polymer, in order to improve adhesion or cohesion, various copolymerizable monomers such as a polar group-containing monomer, a multifunctional monomer, and the like can also be used. Two or more types of copolymerizable monomers may be used in combination. In addition, a crosslinking agent obtained by reacting with a polar group-containing monomer or a multifunctional group-containing monomer may be blended to form a crosslinked structure. In addition, additives such as silane coupling agent and antioxidant can also be blended.
含極性基單體的具體例係可舉例如:(甲基)丙烯酸、衣康酸、順丁烯二酸、反丁烯二酸、巴豆酸、異巴豆酸等含羧基單體或其酐(順丁烯二酸酐等);(甲基)丙烯酸羥乙基、(甲基)丙烯酸羥丙酯、(甲基)丙烯酸羥丁酯等(甲基)丙烯酸羥烷基酯等含羥基單體;(甲基)丙烯醯胺、N,N-二甲基(甲基)丙烯醯胺、N-羥甲基(甲基) 丙烯醯胺、N-甲氧基甲基(甲基)丙烯醯胺、N-丁氧基甲基(甲基)丙烯醯胺等含醯胺基單體;(甲基)丙烯酸胺基乙酯、(甲基)丙烯酸二甲胺基乙酯、(甲基)丙烯酸第三丁胺基乙酯等含胺基單體;(甲基)丙烯酸環氧丙酯、(甲基)丙烯酸甲基環氧丙酯等含環氧丙基單體;(甲基)丙烯腈等含氰基單體;N-乙烯-2-吡咯啶酮、(甲基)丙烯醯基啉、N-乙烯吡啶、N-乙烯哌啶酮、N-乙烯嘧啶、N-乙烯哌、N-乙烯吡咯、N-乙烯咪唑、N-乙烯唑等含雜環乙烯系單體;(甲基)丙烯酸甲氧基乙酯、(甲基)丙烯酸乙氧基乙酯等(甲基)丙烯酸烷氧基烷基酯系單體;乙烯磺酸鈉等含磺酸基單體;丙烯醯基磷酸-2-羥乙酯等含磷酸基單體;環己基順丁烯二醯亞胺、異丙基順丁烯二醯亞胺等含醯亞胺基單體;異氰酸-2-甲基丙烯醯氧基乙酯等含異氰酸酯基單體。其中,較佳係丙烯酸等含羧基單體、丙烯酸羥丁酯等含羥基單體。 Specific examples of polar group-containing monomers include, for example, (meth) acrylic acid, itaconic acid, maleic acid, fumaric acid, crotonic acid, isocrotonic acid, and other carboxyl-containing monomers or their anhydrides ( Maleic anhydride, etc.); hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, hydroxybutyl (meth) acrylate, etc. hydroxyl-containing monomers such as hydroxyalkyl (meth) acrylate; (Meth) acrylamide, N, N-dimethyl (meth) acrylamide, N-hydroxymethyl (meth) acrylamide, N-methoxymethyl (meth) acrylamide , N-butoxymethyl (meth) acrylamide and other amide group-containing monomers; (meth) acrylic acid aminoethyl, (meth) acrylic acid dimethylaminoethyl, (meth) acrylic acid Amino group-containing monomers such as third butylamino ethyl ester; glycidyl (meth) acrylate, methyl glycidyl (meth) acrylate and other glycidyl monomers; (meth) acrylonitrile Cyanide-containing monomers; N-vinyl-2-pyrrolidone, (meth) acryloyl Porphyrin, N-vinylpyridine, N-vinylpiperidone, N-vinylpyrimidine, N-vinylpyridine , N-vinylpyrrole, N-vinylimidazole, N-ethylene Heterocycle-containing vinyl monomers such as azole; alkoxyalkyl (meth) acrylate monomers such as methoxyethyl (meth) acrylate and ethoxyethyl (meth) acrylate; ethylene sulfonic acid Sulfonic acid group-containing monomers such as sodium; phosphoric acid group-containing monomers such as 2-hydroxyethyl propenyl acetyl phosphate; cyclohexyl maleimide diimide, isopropyl maleimide diimide etc. Amine-based monomer; isocyanate group-containing monomer such as isocyanate-2-methacryloxyethyl ester. Among them, carboxyl group-containing monomers such as acrylic acid and hydroxyl group-containing monomers such as hydroxybutyl acrylate are preferred.
含羧基單體係可提升窄邊框接著性、耐荷重性、加工性、窄邊框耐濕熱荷重性等特性。在丙烯酸系聚合物100質量%中,含羧基單體的量較佳係10~20質量%、更佳係10~12質量%。該等範圍的下限值係由窄邊框接著性、耐荷重性、加工性、窄邊框耐濕熱荷重性等而言具意義。又,上限值係由實施各種評價時的黏著帶之初期黏貼性而言具意義。 The carboxyl-containing single system can improve the characteristics of narrow frame adhesion, load resistance, processability, and narrow frame moisture and heat resistance. In 100% by mass of the acrylic polymer, the amount of the carboxyl group-containing monomer is preferably 10 to 20% by mass, and more preferably 10 to 12% by mass. The lower limit of these ranges is meaningful in terms of narrow frame adhesion, load resistance, workability, and narrow frame moisture and heat resistance. In addition, the upper limit value is significant from the initial adhesiveness of the adhesive tape when various evaluations are performed.
含羥基單體係能提升窄邊框接著性、耐荷重性、加工性、窄邊框耐濕熱荷重性等特性。在丙烯酸系聚合物100質量%中,含羥基單體的量較佳係0.01~2.0質量%、更佳係0.05~0.15質量%。該等範圍的上限值係由抑制黏著帶在加熱‧濕熱環境下的經時變化、維持充分之窄邊框接著性、耐荷重性、加工性、窄邊框耐濕熱荷重 等特性的觀點而言具有意義。 The hydroxyl-containing single system can improve the characteristics of narrow frame adhesion, load resistance, processability, and narrow frame resistance to moisture and heat. In 100% by mass of the acrylic polymer, the amount of the hydroxyl group-containing monomer is preferably 0.01 to 2.0% by mass, and more preferably 0.05 to 0.15% by mass. The upper limit of these ranges is from the viewpoint of suppressing the change of the adhesive tape with time under heating and humid environment, maintaining sufficient narrow frame adhesion, load resistance, workability, and narrow frame resistance to humidity and heat load. significance.
黏著劑層的厚度較佳係5~200μm、更佳係10~100μm。 The thickness of the adhesive layer is preferably 5 to 200 μm, and more preferably 10 to 100 μm.
黏著劑層係例如藉由使黏著劑組成物進行交聯反應而可形成。亦即,將黏著劑組成物塗佈於基材上,利用加熱進行交聯反應,可在基材上形成黏著劑層。又,亦可將黏著劑組成物塗佈於離型紙或其他薄膜上,利用加熱施行交聯反應而形成黏著劑層,再將該黏著劑層貼合於基材單面或雙面上。在黏著劑組成物塗佈時,可使用例如:輥塗機、模具塗佈機、唇式塗佈機等塗佈裝置。在塗佈後施行加熱時,在利用加熱進行交聯反應之同時亦可除去黏著劑組成物中的溶劑。另外,黏著劑層最好未含有賦黏樹脂。 The adhesive layer can be formed, for example, by subjecting the adhesive composition to a cross-linking reaction. That is, the adhesive composition is coated on the substrate, and the cross-linking reaction is performed by heating to form an adhesive layer on the substrate. Alternatively, the adhesive composition may be coated on a release paper or other film, and a cross-linking reaction may be performed by heating to form an adhesive layer, and then the adhesive layer may be attached to one side or both sides of the substrate. When coating the adhesive composition, a coating device such as a roll coater, die coater, lip coater, etc. can be used. When heating is applied after coating, the solvent in the adhesive composition can also be removed while the crosslinking reaction is performed by heating. In addition, the adhesive layer preferably does not contain an adhesive resin.
本發明黏著帶係在基材單面或雙面上設有黏著劑層。黏著劑層亦可僅形成於基材單面,但最好設為雙面均形成的雙面黏著帶。 The adhesive tape of the invention is provided with an adhesive layer on one side or both sides of the substrate. The adhesive layer may be formed only on one side of the substrate, but it is preferably a double-sided adhesive tape formed on both sides.
本發明黏著帶在依0.3~5.0MPa範圍內經壓縮時,接著時壓縮變形率係0~-10%、較佳係0~-8%。又,在0.3~5.0MPa範圍內施行壓縮後,接著時壓縮變形率的維持率較佳係±3%以內、更佳係±2%以內。 When the adhesive tape of the present invention is compressed within the range of 0.3 to 5.0 MPa, the compression deformation rate is 0 to -10%, preferably 0 to -8%. In addition, after the compression is performed in the range of 0.3 to 5.0 MPa, the retention rate of the compression deformation rate during the subsequent period is preferably within ± 3%, and more preferably within ± 2%.
本發明黏著帶的最低損失正切較佳係在50~100℃範圍內,且最低損失正切與150℃損失正切之差較佳在1.5×10-1以下。最低損失正切在50~100℃範圍內,係對動態接著力與剝離位移而言具有意義。又,最低損失正切與150℃損失正切之差在1.5×10-1以下,係對接著時壓縮變形率、動態接著力及剝離位移而言具有意義。 The minimum loss tangent of the adhesive tape of the present invention is preferably in the range of 50-100 ° C, and the difference between the minimum loss tangent and the loss tangent of 150 ° C is preferably 1.5 × 10 -1 or less. The minimum loss tangent is in the range of 50 ~ 100 ℃, which is meaningful for dynamic adhesive force and peeling displacement. In addition, the difference between the minimum loss tangent and the loss tangent at 150 ° C is 1.5 × 10 -1 or less, which is significant for the compression deformation rate, dynamic adhesive force, and peeling displacement at the time of bonding.
本發明黏著帶的儲存彈性模數變化點α,較佳達100 ℃以上。又,依每分鐘1mm進行拉伸時的荷重-位移曲線中,基材未發生層間破壞,最大荷重值較佳係達40N/cm2以上,且剝離位移較佳在2.0mm以下。 The storage elastic modulus change point α of the adhesive tape of the present invention is preferably above 100 ° C. In addition, in the load-displacement curve when stretching at 1 mm per minute, no interlayer failure occurs in the substrate, the maximum load value is preferably 40 N / cm 2 or more, and the peeling displacement is preferably 2.0 mm or less.
本發明黏著帶根據JIS K-7181的壓縮強度測定進行測定時,40%壓縮強度較佳係2MPa以上、更佳係2~5MPa。 When the adhesive tape of the present invention is measured according to the compressive strength measurement of JIS K-7181, the 40% compressive strength is preferably 2 MPa or more, and more preferably 2 to 5 MPa.
以上所說明各物性值的具體測定條件,係如後述實施例所記載。 The specific measurement conditions for each physical property value described above are as described in the examples described below.
本發明黏著帶係可依0.1~5.0MPa的非常高壓力施行壓合。特別從其尺寸安定性而言,最適合用於窄幅黏著帶。所以,在需要此種特性的領域中能有效使用於各種用途。具體而言,可非常有效使用為構造接著用黏著帶、電子機器接著用黏著帶。 The adhesive tape of the present invention can be pressed at a very high pressure of 0.1 to 5.0 MPa. Especially in terms of its size stability, it is most suitable for narrow width adhesive tapes. Therefore, it can be effectively used for various applications in fields where such characteristics are required. Specifically, it can be used very effectively as a structure followed by an adhesive tape and an electronic device followed by an adhesive tape.
以下,舉實施例與比較例,針對本發明進行更詳細說明。以下記載中,「份」係指質量份,「%」係指質量%。 Hereinafter, the present invention will be described in more detail with examples and comparative examples. In the following description, "parts" means mass parts, and "%" means mass%.
在具備有攪拌機、溫度計、回流冷卻器及氮氣導入管的反應裝置中,裝填入表1所示量(%)的成分(A1)~(A5)、醋酸乙酯、鏈轉移劑之正十二烷硫醇、以及過氧化物系自由基聚合起始劑之過氧化月桂基0.1份。在反應裝置內封入氮氣,一邊攪拌,一邊在氮氣流下,於68℃下進行3小時聚合反應,然後78℃下進行3小時聚合反應。接著,冷卻至室溫,添加醋酸乙酯。藉此獲得固形份濃度30%的丙烯酸系共聚合體(A)。 In a reaction device equipped with a stirrer, thermometer, reflux cooler, and nitrogen introduction tube, fill the components (A1) to (A5), ethyl acetate, and chain transfer agent in the amount (%) shown in Table 1 0.1 parts of lauryl peroxide of dialkyl mercaptan and peroxide-based radical polymerization initiator. Nitrogen was sealed in the reaction apparatus, and the polymerization reaction was carried out at 68 ° C. for 3 hours under a nitrogen flow while stirring, and then at 78 ° C. for 3 hours. Next, it was cooled to room temperature, and ethyl acetate was added. Thus, an acrylic copolymer (A) having a solid content concentration of 30% was obtained.
各丙烯酸系共聚合體的重量平均分子量(Mw)及理論 Tg如表1所示。該重量平均分子量(Mw)係利用GPC法,依下述測定裝置及條件,測定丙烯酸系共聚合體之標準聚苯乙烯換算分子量的值。 Table 1 shows the weight average molecular weight (Mw) and theoretical Tg of each acrylic copolymer. This weight-average molecular weight (Mw) is the value of the standard polystyrene-equivalent molecular weight of the acrylic copolymer measured by the GPC method according to the following measuring device and conditions.
‧裝置:LC-2000系列(日本分光股份有限公司製) ‧Apparatus: LC-2000 series (manufactured by JASCO Corporation)
‧管柱:Shodex KF-806M×2支、Shodex KF-802×1支 ‧Tube: Shodex KF-806M × 2pcs, Shodex KF-802 × 1pcs
‧洗提液:四氫呋喃(THF) ‧Eluent: Tetrahydrofuran (THF)
‧流速:1.0mL/分 ‧Flow rate: 1.0mL / min
‧管柱溫度:40℃ ‧Column temperature: 40 ℃
‧注入量:100μL ‧Injection volume: 100μL
‧檢測器:折射率計(RI) ‧Detector: Refractometer (RI)
‧測定樣品:使丙烯酸系聚合物溶解於THF中,製作丙烯酸系聚合物濃度0.5質量%的溶液,利用過濾器進行過濾而除去雜物。 ‧Measurement sample: Dissolve the acrylic polymer in THF to prepare a solution with an acrylic polymer concentration of 0.5% by mass, and filter with a filter to remove impurities.
理論Tg係從FOX公式計算出的值。 The theoretical Tg is the value calculated from the FOX formula.
表1中的代號係如下:「MA」:丙烯酸甲酯 The code names in Table 1 are as follows: "MA": methyl acrylate
「2-EHA」:丙烯酸-2-乙基己酯 "2-EHA": 2-ethylhexyl acrylate
「BA」:丙烯酸正丁酯 "BA": n-butyl acrylate
「AA」:丙烯酸 "AA": Acrylic
「4-HBA」:丙烯酸-4-羥丁酯 "4-HBA": 4-hydroxybutyl acrylate
「Vac」:醋酸乙烯酯 "Vac": vinyl acetate
然後,相對於各丙烯酸系共聚合體(A)固形份100份,添加:交聯劑(B)之東曹股份有限公司製異氰酸酯系交聯劑(CORONATE(註冊商標)L-45E、45%溶液)0.04份、矽烷偶合劑(C)之信越化學工業公司製矽烷偶合劑(商品名KBM-403)0.1份、以及抗氧化劑(D)之BASF公司製抗氧化劑(IRGANOX(註冊商標)1010)0.1份,經混合製備得黏著劑組成物。其次,在110℃下施行溶劑除去‧乾燥,且進行交聯反應,將黏著劑組成物在經聚矽氧處理過的離型紙上,依乾燥後厚度成為0.075mm方式塗佈。 Then, with respect to 100 parts of the solid content of each acrylic copolymer (A), a crosslinking agent (B), an isocyanate crosslinking agent (CORONATE (registered trademark) L-45E, 45% solution manufactured by Tosoh Corporation) was added ) 0.04 parts, 0.1 part of the silane coupling agent (C) made by Shin-Etsu Chemical Co., Ltd., silane coupling agent (trade name KBM-403), and antioxidant (D) made by BASF company (IRGANOX (registered trademark) 1010) Parts, the adhesive composition is prepared by mixing. Secondly, the solvent was removed and dried at 110 ° C, and a cross-linking reaction was carried out. The adhesive composition was coated on the silicone-treated release paper so that the thickness after drying would be 0.075 mm.
首先,準備由含乙烯-醋酸乙烯酯共聚合體之聚乙烯(PE)系發泡體構成的基材[厚度=0.15mm、拉伸彈性模數=46.1N/mm2、彎曲力矩(MD方向)=16gf/cm、(TD方向)=17gf/cm、發泡倍率=1.9、密度=544kg/m3],其為未含孔隙(不良氣泡)的基材。然後,對該基材雙面施行電暈放電處理,在基材雙面上貼合製造例1所獲得之離型紙上的黏著劑層,於40℃下進行3日熟化,獲得雙面黏著帶。 First, prepare a base material composed of a polyethylene (PE) foam containing an ethylene-vinyl acetate copolymer [thickness = 0.15 mm, tensile modulus of elasticity = 46.1 N / mm 2 , bending moment (MD direction) = 16gf / cm, (TD direction) = 17gf / cm, expansion ratio = 1.9, density = 544kg / m 3], which is not included voids (bubbles defective) substrate. Then, the substrate was subjected to corona discharge treatment on both sides, and the adhesive layer on the release paper obtained in Production Example 1 was laminated on both sides of the substrate, and cured at 40 ° C for 3 days to obtain a double-sided adhesive tape .
除黏著劑層係使用製造例2與3所獲得黏著劑層之外,其餘均依照與實施例1同樣地獲得雙面黏著帶。 A double-sided adhesive tape was obtained in the same manner as in Example 1, except that the adhesive layer was obtained using the adhesive layers obtained in Production Examples 2 and 3.
除基材係使用PE系發泡體[厚度=0.2mm、拉伸彈性模數=21.0N/mm2、彎曲力矩(MD方向)=3gf/cm、(TD方向)=4gf/cm、發泡倍率=3、密度=330kg/m3],且黏著劑層經乾燥後的厚度成為0.05mm之外,其餘均依照與實施例1同樣地獲得雙面黏著帶。 In addition to the base material, PE foam is used [thickness = 0.2 mm, tensile modulus of elasticity = 21.0 N / mm 2 , bending moment (MD direction) = 3 gf / cm, (TD direction) = 4 gf / cm, foam Magnification = 3, density = 330 kg / m 3 ], and the thickness of the adhesive layer after drying became 0.05 mm, and the rest was obtained in the same manner as in Example 1 to obtain a double-sided adhesive tape.
除基材係使用PE系發泡體[厚度=0.15mm、拉伸彈性模數=23.7N/mm2、彎曲力矩(MD方向)=7gf/cm、(TD方向)=8gf/cm、發泡倍率=1.8、密度=560kg/m3]之外,其餘均依照與實施例1同樣地獲得雙面黏著帶。 Except for the base material, PE foam is used [thickness = 0.15mm, tensile modulus of elasticity = 23.7N / mm 2 , bending moment (MD direction) = 7gf / cm, (TD direction) = 8gf / cm, foam Except for magnification = 1.8 and density = 560 kg / m 3 ], the rest of the adhesive tape was obtained in the same manner as in Example 1.
實施例及比較例的基材拉伸彈性模數、以及基材與黏著帶的彎曲力矩,係依照以下方法測定的值。各測定值係如表2所示。 The tensile modulus of elasticity of the substrate and the bending moment of the substrate and the adhesive tape in Examples and Comparative Examples are values measured according to the following methods. The measured values are shown in Table 2.
將基材裁剪為寬(W)10mm、長70mm的短片狀(長邊為MD方向),將其使用為測試片。然後,依1/100量錶(N=5)測定厚度,將5處的平均值設為厚度(t),並從下式求取測試片的截面積(S)。 The base material was cut into a short sheet shape with a width (W) of 10 mm and a length of 70 mm (the long side was in the MD direction), and it was used as a test piece. Then, the thickness was measured in accordance with a 1/100 scale (N = 5), and the average value at 5 points was regarded as the thickness (t), and the cross-sectional area (S) of the test piece was obtained from the following formula.
截面積S(mm2)=t×W Cross-sectional area S (mm 2 ) = t × W
t:厚度(mm) t: thickness (mm)
W:寬度(mm) W: width (mm)
根據JIS K7161 2014,將市售之拉伸測試裝置(東洋精機製作所公司製、裝置名Strograph V-10C、全幅50N)的夾具間隔 (L)設定為20mm,夾住測試片的上端與下端。然後,依拉伸速度10mm/分進行拉伸,獲得拉伸荷重-位移曲線。從所獲得拉伸荷重-位移曲線的位移0.05mm與0.25mm之拉伸荷重,求取直線式。從所獲得直線式求取拉伸荷重F=10N時的位移x(mm),再從下式求取成為基材剛性指標的拉伸彈性模數。 According to JIS K7161 2014, the clamp interval (L) of a commercially available tensile test device (manufactured by Toyo Seiki Co., Ltd., device name Strograph V-10C, full width 50N) was set to 20 mm, and the upper and lower ends of the test piece were sandwiched. Then, stretching was performed at a stretching speed of 10 mm / min to obtain a tensile load-displacement curve. From the tensile load of the obtained tensile load-displacement curve with displacements of 0.05 mm and 0.25 mm, a linear formula is obtained. The displacement x (mm) when the tensile load F = 10N is obtained from the obtained linear formula, and then the tensile elastic modulus which is an index of the rigidity of the substrate is obtained from the following formula.
拉伸彈性模數(N/mm2)=(F/S)/(x/L) Tensile elastic modulus (N / mm 2 ) = (F / S) / (x / L)
F:拉伸荷重=10(N) F: Tensile load = 10 (N)
S:截面積(mm2) S: Cross-sectional area (mm 2 )
x:拉伸荷重=10N時的位移(mm) x: displacement when tensile load = 10N (mm)
L:夾具間隔=20(mm) L: fixture interval = 20 (mm)
另外,各直線式及拉伸彈性模數係如下。 In addition, each linear formula and tensile elastic modulus system are as follows.
實施例1~3:直線式y=3.6667x+0.0767、拉伸彈性模數46.1N/mm2 Examples 1 to 3: Linear type y = 3.6667x + 0.0767, tensile elastic modulus 46.1N / mm 2
比較例1:直線式y=1.2632x-0.0432、拉伸彈性模數21.0N/mm2 Comparative Example 1: Linear formula y = 1.2632x-0.0432, tensile modulus of elasticity 21.0N / mm 2
比較例2:直線式y=2.1026x+0.1349、拉伸彈性模數23.7N/mm2 Comparative Example 2: Linear formula y = 2.1026x + 0.1349, tensile modulus of elasticity 23.7N / mm 2
將基材(或雙面黏著帶)11裁剪為寬38mm、長50mm的短片狀,將其使用為測試片。所獲得測試片如圖1所示利用4支端子12夾住。然後,根據JIS P8125,設置於市售塔柏剛性度測試機(Taber stiffness tester,東洋精機製作所公司製)之測試時進行運轉的部分,在擺錘安裝10g錘,讀取彎曲速度3°/sec、彎曲角度15°時的刻度,將其設為測定值。然後,將該測定值代入以下計算式,計算出MD方向與TD方向的彎曲力矩(M)。 The base material (or double-sided adhesive tape) 11 was cut into a short piece having a width of 38 mm and a length of 50 mm, and used as a test piece. The obtained test piece is sandwiched by four terminals 12 as shown in FIG. 1. Then, according to JIS P8125, it is installed in the part that is operated during the test of a commercially available Taber stiffness tester (manufactured by Toyo Seiki Co., Ltd.), a 10 g hammer is attached to the pendulum, and the bending speed is read at 3 ° / sec , Scale at a bending angle of 15 °, and set it as the measured value. Then, the measured value is substituted into the following calculation formula to calculate the bending moment (M) in the MD direction and the TD direction.
彎曲力矩(gf/cm)=38.0nk/w Bending moment (gf / cm) = 38.0nk / w
n:所讀取刻度(10g錘時為1) n: scale read (1 at 10g hammer)
k:每一刻度的力矩(gf/cm) k: torque per scale (gf / cm)
w:測試片寬度 w: width of test piece
針對實施例及比較例所獲得雙面黏著帶,依照以下方法施行評價。結果如表3~6所示。 The double-sided adhesive tapes obtained in Examples and Comparative Examples were evaluated according to the following methods. The results are shown in Tables 3-6.
將實施例與比較例所獲得雙面黏著帶加工為10mm×10mm正方形狀,利用厚度75μm白色PET薄膜從二側夾入,利用壓合機施行加壓。此時,依實際施加於黏著帶的壓力成為0.3MPa、0.5MPa、1.0MPa、1.5MPa、2.0MPa、4.0MPa、5.0MPa的各條件施行加壓。 The double-sided adhesive tapes obtained in Examples and Comparative Examples were processed into a square shape of 10 mm × 10 mm, sandwiched from both sides by a white PET film with a thickness of 75 μm, and pressurized by a pressing machine. At this time, pressurization is performed under the conditions that the pressure actually applied to the adhesive tape becomes 0.3 MPa, 0.5 MPa, 1.0 MPa, 1.5 MPa, 2.0 MPa, 4.0 MPa, 5.0 MPa.
經該加壓後,於5分鐘以內,利用KEYENCE公司製雷射掃描顯微鏡VK-X260觀察帶截面並測定厚度。然後,由下式計算出接著時的壓縮變形率。 After this pressurization, within 5 minutes, the tape cross section was observed using a laser scanning microscope VK-X260 manufactured by KEYENCE, and the thickness was measured. Then, the compression deformation rate at the next time was calculated from the following formula.
(接著時壓縮變形率)=(加壓前厚度-加壓後厚度)/(加壓前厚度)×100[%] (Compression deformation rate at the time) = (Thickness before compression-Thickness after compression) / (Thickness before compression) × 100 [%]
將經測定接著時壓縮變形率後的各雙面黏著帶,在23℃、50%RH下保存24小時。然後,利用KEYENCE公司製雷射掃描顯微鏡VK-X260觀察帶截面,並測定厚度。接著,由下式計算出接著時壓縮變形率之維持率。 The double-sided adhesive tapes after compressive deformation at the time of measurement were stored at 23 ° C. and 50% RH for 24 hours. Then, the belt section was observed using a laser scanning microscope VK-X260 manufactured by KEYENCE, and the thickness was measured. Next, the maintenance rate of the compression deformation rate at the time of adhesion is calculated from the following formula.
(接著時壓縮變形率之維持率)=(加壓後保存24小時後的厚度-剛加壓後的厚度)/(剛加壓後的厚度)×100[%] (Retention rate of compression deformation rate at the time of next) = (Thickness after 24 hours of storage after pressing-Thickness immediately after pressing) / (Thickness immediately after pressing) × 100 [%]
將實施例及比較例所獲得雙面黏著帶重疊至厚度成為2mm為止,使用動態黏彈性測定裝置(TA Instruments Japan(股)製、RDA-III),且夾具係使用平行板8mm,在頻率10Hz、測定溫度-50℃~150℃、升溫速度10℃/分條件下測定動態黏彈性,獲得如圖2所示主曲線,而獲得儲存彈性模數變化點α、最低損失正切、150℃損失正切。 The double-sided adhesive tapes obtained in the examples and the comparative examples were overlapped to a thickness of 2 mm, a dynamic viscoelasticity measuring device (TA Instruments Japan Co., Ltd., RDA-III) was used, and a parallel plate was used for the jig 8mm, the dynamic viscoelasticity is measured under the conditions of frequency 10Hz, measuring temperature -50 ℃ ~ 150 ℃, heating rate 10 ℃ / min, the main curve shown in Figure 2 is obtained, and the storage elastic modulus change point α and the minimum loss tangent , Loss tangent at 150 ℃.
將實施例及比較例所獲得雙面黏著帶裁剪為10mm×10mm尺 寸,撕開其中一離型紙。然後,如圖3所示,在SUS304製T字夾具32上貼合雙面黏著帶31,接著撕開另一離型紙,貼合於長125mm、寬50mm、厚2.0mm的玻璃板33上。依0.5MPa施行10秒鐘加壓,然後於5分鐘以內,在23℃、50%RH環境下,依1mm/分的速度朝上方向拉伸,獲得荷重-位移曲線。從所獲得曲線測定最大荷重、與貼合部分剝離時的位移mm。 The double-sided adhesive tapes obtained in Examples and Comparative Examples were cut to a size of 10 mm × 10 mm, and one of the release papers was torn apart. Then, as shown in FIG. 3, the double-sided adhesive tape 31 was attached to a T-shaped jig 32 made of SUS304, and then another release paper was ripped to be attached to a glass plate 33 having a length of 125 mm, a width of 50 mm, and a thickness of 2.0 mm. Apply pressure at 0.5MPa for 10 seconds, then within 5 minutes, under 23 ℃, 50% RH environment, at a speed of 1mm / min in the upward direction to obtain a load-displacement curve. From the obtained curve, the maximum load and the displacement mm at the time of peeling off from the bonded portion were measured.
將實施例及比較例所獲得雙面黏著帶重疊至厚度成為12mm為止,使用壓縮強度測定裝置(島津製作所(股)製、AG-20kNX),且測定(解析)軟體係使用Trapezium X,測定模式係設為單一條件(single condition),根據JIS K-7181測定0~50%壓縮強度,製成主曲線,獲得40%及50%壓縮強度。 The double-sided adhesive tapes obtained in the Examples and Comparative Examples were superimposed to a thickness of 12 mm, a compressive strength measuring device (Shimadzu Corporation, AG-20kNX) was used, and the measurement (analysis) soft system used Trapezium X, measurement mode The system is set to a single condition, and the 0-50% compressive strength is measured according to JIS K-7181, and the main curve is prepared to obtain 40% and 50% compressive strength.
由表3~5的評價結果得知,實施例1~3的雙面黏著帶係完全無關於40%及50%壓縮強度,所有特性均優異。 From the evaluation results of Tables 3 to 5, it is known that the double-sided adhesive tapes of Examples 1 to 3 have no compressive strength of 40% and 50% at all, and all the characteristics are excellent.
比較例1與2的雙面黏著帶,因為接著時壓縮變形率大,因而如圖4(A)所示,在加壓步驟中,因雙面黏著帶41的厚度尺寸變化,導致蓋板42與框體43的間隙G變大,一體感降低,有大幅損及原本外觀的可能性。又,比較例1與2的雙面黏著帶,因為在0.1MPa~5.0MPa各壓力下的接著時壓縮變形率差,因而難以預測間隙G而設計蓋板42與框體43。 The double-sided adhesive tapes of Comparative Examples 1 and 2 have a large compression deformation rate during the subsequent bonding process. Therefore, as shown in FIG. 4 (A), in the pressing step, the thickness of the double-sided adhesive tape 41 changes, resulting in the cover 42 The gap G with the frame 43 becomes larger, the sense of unity is reduced, and the original appearance may be greatly impaired. In addition, in the double-sided adhesive tapes of Comparative Examples 1 and 2, since the compression deformation rate at the time of each pressure under 0.1 MPa to 5.0 MPa is poor, it is difficult to predict the gap G and design the cover 42 and the frame 43.
比較例1的雙面黏著帶,因為接著時壓縮變形率之維持率大(無法維持變形),因而即使預測間隙G而設計蓋板42與框體43, 仍如圖4(B)所示,有蓋板42從框體43蹦出的可能性。 The double-sided adhesive tape of Comparative Example 1 has a large retention rate of compression deformation rate (the deformation cannot be maintained). Therefore, even if the cover 42 and the frame 43 are designed to predict the gap G, it is still as shown in FIG. 4 (B). There is a possibility that the cover 42 pops out of the frame 43.
比較例1與2的雙面黏著帶中,因為儲存彈性模數變化點α在100℃以下,因而更難以預測間隙G而設計蓋板42與框體43。又,比較例1的雙面黏著帶,因為由拉伸力所造成的荷重-位移曲線之最大荷重較低,因而有容易因拉伸力而發生剝落的傾向。 In the double-sided adhesive tapes of Comparative Examples 1 and 2, since the storage elastic modulus change point α is below 100 ° C., it is more difficult to predict the gap G and design the cover 42 and the frame 43. In addition, the double-sided adhesive tape of Comparative Example 1 has a tendency to peel off easily due to the tensile force because the maximum load of the load-displacement curve due to the tensile force is low.
本發明的黏著帶係無關於40%與50%壓縮強度,接著時的壓縮變形率均小,因而在需要此種特性的領域中,可利用於各種用途。特別適用於智慧手機、平板終端機等電子機器用途。具體係可使用於框體與蓋板的固定、以及車用LCD與框體的固定等。 The adhesive tape of the present invention has no compressive strength of 40% and 50%, and the compressive deformation rate at the time of bonding is small, so that it can be used for various applications in fields where such characteristics are required. Especially suitable for electronic devices such as smart phones and tablet terminals. Specifically, it can be used for fixing the frame and the cover, and fixing the LCD for the vehicle and the frame.
Claims (13)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JPPCT/JP2017/026870 | 2017-07-25 | ||
| PCT/JP2017/026870 WO2019021371A1 (en) | 2017-07-25 | 2017-07-25 | Adhesive tape |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW201908443A true TW201908443A (en) | 2019-03-01 |
Family
ID=65040018
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW107125746A TW201908443A (en) | 2017-07-25 | 2018-07-25 | Adhesive tape |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JP7130312B2 (en) |
| KR (1) | KR20200026281A (en) |
| CN (1) | CN110959030A (en) |
| TW (1) | TW201908443A (en) |
| WO (1) | WO2019021371A1 (en) |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4623198Y1 (en) | 1968-07-11 | 1971-08-10 | ||
| JPS5947870B2 (en) | 1976-08-18 | 1984-11-21 | 株式会社八光電機製作所 | pipe heater |
| JPS5332107A (en) | 1976-09-06 | 1978-03-27 | Kitasato Inst | Preparation of bioactive substance from angelica acutiloba kit azawa |
| JPS5991178A (en) * | 1982-11-15 | 1984-05-25 | Sekisui Chem Co Ltd | Foamed self-adhesive tape or sheet |
| JPS6426692A (en) * | 1987-04-06 | 1989-01-27 | Toray Industries | Adhesive tape |
| JP3817768B2 (en) * | 1996-03-08 | 2006-09-06 | 東レ株式会社 | Laminate and adhesive tape |
| WO2013154137A1 (en) * | 2012-04-13 | 2013-10-17 | Dic株式会社 | Adhesive tape |
| JP2015046526A (en) | 2013-08-29 | 2015-03-12 | 京セラ株式会社 | Electronics |
| CN111690165B (en) * | 2014-09-24 | 2023-02-28 | 日东电工株式会社 | Foamed sheet |
| CN106715550B (en) * | 2014-09-30 | 2020-06-05 | 积水化学工业株式会社 | Polyolefin resin foam sheet and adhesive tape |
| JP2017002292A (en) * | 2015-06-15 | 2017-01-05 | 日東電工株式会社 | Adhesive sheet |
| JP6224169B2 (en) | 2015-06-15 | 2017-11-01 | 日東電工株式会社 | Fixing member and portable electronic device |
| JP6010721B1 (en) * | 2015-08-25 | 2016-10-19 | 株式会社寺岡製作所 | Adhesive tape |
-
2017
- 2017-07-25 WO PCT/JP2017/026870 patent/WO2019021371A1/en not_active Ceased
- 2017-07-25 KR KR1020207003273A patent/KR20200026281A/en not_active Ceased
- 2017-07-25 JP JP2019532251A patent/JP7130312B2/en active Active
- 2017-07-25 CN CN201780093543.4A patent/CN110959030A/en active Pending
-
2018
- 2018-07-25 TW TW107125746A patent/TW201908443A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JPWO2019021371A1 (en) | 2020-07-02 |
| WO2019021371A1 (en) | 2019-01-31 |
| JP7130312B2 (en) | 2022-09-05 |
| CN110959030A (en) | 2020-04-03 |
| KR20200026281A (en) | 2020-03-10 |
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