KR20150087293A - 고도로 점착부여된 아크릴레이트 감압 접착제 - Google Patents
고도로 점착부여된 아크릴레이트 감압 접착제 Download PDFInfo
- Publication number
- KR20150087293A KR20150087293A KR1020157015804A KR20157015804A KR20150087293A KR 20150087293 A KR20150087293 A KR 20150087293A KR 1020157015804 A KR1020157015804 A KR 1020157015804A KR 20157015804 A KR20157015804 A KR 20157015804A KR 20150087293 A KR20150087293 A KR 20150087293A
- Authority
- KR
- South Korea
- Prior art keywords
- acrylate
- weight
- parts
- copolymerized
- pressure sensitive
- 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.)
- Ceased
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- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 title claims abstract description 197
- 239000004820 Pressure-sensitive adhesive Substances 0.000 title claims abstract description 145
- 229920000642 polymer Polymers 0.000 claims abstract description 185
- 239000000178 monomer Substances 0.000 claims abstract description 160
- 230000005855 radiation Effects 0.000 claims abstract description 124
- 239000002243 precursor Substances 0.000 claims abstract description 99
- 229920005989 resin Polymers 0.000 claims abstract description 79
- 239000011347 resin Substances 0.000 claims abstract description 79
- 238000000034 method Methods 0.000 claims abstract description 42
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 34
- 238000004132 cross linking Methods 0.000 claims description 110
- 239000000203 mixture Substances 0.000 claims description 91
- 239000003431 cross linking reagent Substances 0.000 claims description 43
- 229920005601 base polymer Polymers 0.000 claims description 32
- 239000000758 substrate Substances 0.000 claims description 28
- 238000002156 mixing Methods 0.000 claims description 24
- 239000010410 layer Substances 0.000 claims description 23
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 20
- 230000003068 static effect Effects 0.000 claims description 17
- 238000012360 testing method Methods 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 239000002390 adhesive tape Substances 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical group CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims description 8
- LTYBJDPMCPTGEE-UHFFFAOYSA-N (4-benzoylphenyl) prop-2-enoate Chemical compound C1=CC(OC(=O)C=C)=CC=C1C(=O)C1=CC=CC=C1 LTYBJDPMCPTGEE-UHFFFAOYSA-N 0.000 claims description 6
- 150000008365 aromatic ketones Chemical class 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 claims description 5
- FLKHVLRENDBIDB-UHFFFAOYSA-N 2-(butylcarbamoyloxy)ethyl prop-2-enoate Chemical compound CCCCNC(=O)OCCOC(=O)C=C FLKHVLRENDBIDB-UHFFFAOYSA-N 0.000 claims description 5
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 5
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 5
- 150000004056 anthraquinones Chemical class 0.000 claims description 5
- QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- OQADFQIQGRQTGW-UHFFFAOYSA-N (4-benzoyl-1-chloro-5,6-diethoxycyclohexa-2,4-dien-1-yl) prop-2-enoate Chemical compound C1=CC(OC(=O)C=C)(Cl)C(OCC)C(OCC)=C1C(=O)C1=CC=CC=C1 OQADFQIQGRQTGW-UHFFFAOYSA-N 0.000 claims description 4
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 claims description 3
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 claims description 3
- IXPWKHNDQICVPZ-UHFFFAOYSA-N 2-methylhex-1-en-3-yne Chemical compound CCC#CC(C)=C IXPWKHNDQICVPZ-UHFFFAOYSA-N 0.000 claims description 3
- XUYDVDHTTIQNMB-UHFFFAOYSA-N 3-(diethylamino)propyl prop-2-enoate Chemical compound CCN(CC)CCCOC(=O)C=C XUYDVDHTTIQNMB-UHFFFAOYSA-N 0.000 claims description 3
- UFQHFMGRRVQFNA-UHFFFAOYSA-N 3-(dimethylamino)propyl prop-2-enoate Chemical compound CN(C)CCCOC(=O)C=C UFQHFMGRRVQFNA-UHFFFAOYSA-N 0.000 claims description 3
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- GVBMMNAPRZDGEY-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-2-methylprop-2-enamide Chemical compound CCN(CC)CCNC(=O)C(C)=C GVBMMNAPRZDGEY-UHFFFAOYSA-N 0.000 claims description 3
- CXSANWNPQKKNJO-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]prop-2-enamide Chemical compound CCN(CC)CCNC(=O)C=C CXSANWNPQKKNJO-UHFFFAOYSA-N 0.000 claims description 3
- DCBBWYIVFRLKCD-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-2-methylprop-2-enamide Chemical compound CN(C)CCNC(=O)C(C)=C DCBBWYIVFRLKCD-UHFFFAOYSA-N 0.000 claims description 3
- WDQKICIMIPUDBL-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]prop-2-enamide Chemical compound CN(C)CCNC(=O)C=C WDQKICIMIPUDBL-UHFFFAOYSA-N 0.000 claims description 3
- VNLHOYZHPQDOMS-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-2-methylprop-2-enamide Chemical compound CCN(CC)CCCNC(=O)C(C)=C VNLHOYZHPQDOMS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 150000003512 tertiary amines Chemical group 0.000 claims description 3
- JNDVNJWCRZQGFQ-UHFFFAOYSA-N 2-methyl-N,N-bis(methylamino)hex-2-enamide Chemical compound CCCC=C(C)C(=O)N(NC)NC JNDVNJWCRZQGFQ-UHFFFAOYSA-N 0.000 claims description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims 1
- 239000012688 phosphorus precursor Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 5
- 230000001070 adhesive effect Effects 0.000 description 41
- 239000000853 adhesive Substances 0.000 description 40
- 239000012943 hotmelt Substances 0.000 description 40
- 125000000217 alkyl group Chemical group 0.000 description 34
- -1 n- pentyl Chemical group 0.000 description 26
- 238000000576 coating method Methods 0.000 description 19
- 238000012546 transfer Methods 0.000 description 17
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 14
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 14
- 239000012790 adhesive layer Substances 0.000 description 14
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 14
- 239000003999 initiator Substances 0.000 description 14
- 239000000463 material Substances 0.000 description 14
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 14
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 13
- 239000004698 Polyethylene Substances 0.000 description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 13
- 229920000573 polyethylene Polymers 0.000 description 13
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- 150000002148 esters Chemical class 0.000 description 12
- 230000009477 glass transition Effects 0.000 description 12
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 11
- 238000009472 formulation Methods 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 229920001577 copolymer Polymers 0.000 description 10
- 238000006116 polymerization reaction Methods 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 9
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 9
- 229910001220 stainless steel Inorganic materials 0.000 description 9
- 229920001567 vinyl ester resin Polymers 0.000 description 9
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 8
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 8
- 238000007757 hot melt coating Methods 0.000 description 8
- 239000010935 stainless steel Substances 0.000 description 8
- 238000001125 extrusion Methods 0.000 description 7
- 229920001519 homopolymer Polymers 0.000 description 7
- 239000000852 hydrogen donor Substances 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 239000012965 benzophenone Substances 0.000 description 6
- 239000004014 plasticizer Substances 0.000 description 6
- 239000000126 substance Substances 0.000 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 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- 229920006037 cross link polymer Polymers 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 235000007586 terpenes Nutrition 0.000 description 5
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 4
- ZVYGIPWYVVJFRW-UHFFFAOYSA-N 3-methylbutyl prop-2-enoate Chemical compound CC(C)CCOC(=O)C=C ZVYGIPWYVVJFRW-UHFFFAOYSA-N 0.000 description 4
- BDMYQVMQTKUZNB-UHFFFAOYSA-N 4-methylpentyl prop-2-enoate Chemical compound CC(C)CCCOC(=O)C=C BDMYQVMQTKUZNB-UHFFFAOYSA-N 0.000 description 4
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 4
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 239000013032 Hydrocarbon resin Substances 0.000 description 4
- 239000012711 adhesive precursor Substances 0.000 description 4
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- 239000012986 chain transfer agent Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 4
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 4
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 4
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- 229920006270 hydrocarbon resin Polymers 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000010128 melt processing Methods 0.000 description 4
- 229940065472 octyl acrylate Drugs 0.000 description 4
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 4
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 4
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 4
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 150000003505 terpenes Chemical class 0.000 description 4
- RXBOCDZLKBPILN-UHFFFAOYSA-N 2-propylheptyl prop-2-enoate Chemical compound CCCCCC(CCC)COC(=O)C=C RXBOCDZLKBPILN-UHFFFAOYSA-N 0.000 description 3
- IUNVCWLKOOCPIT-UHFFFAOYSA-N 6-methylheptylsulfanyl 2-hydroxyacetate Chemical compound CC(C)CCCCCSOC(=O)CO IUNVCWLKOOCPIT-UHFFFAOYSA-N 0.000 description 3
- CGSLYBDCEGBZCG-UHFFFAOYSA-N Octicizer Chemical compound C=1C=CC=CC=1OP(=O)(OCC(CC)CCCC)OC1=CC=CC=C1 CGSLYBDCEGBZCG-UHFFFAOYSA-N 0.000 description 3
- JOBBTVPTPXRUBP-UHFFFAOYSA-N [3-(3-sulfanylpropanoyloxy)-2,2-bis(3-sulfanylpropanoyloxymethyl)propyl] 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(COC(=O)CCS)(COC(=O)CCS)COC(=O)CCS JOBBTVPTPXRUBP-UHFFFAOYSA-N 0.000 description 3
- 239000002313 adhesive film Substances 0.000 description 3
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 3
- 150000008366 benzophenones Chemical class 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 230000001143 conditioned effect Effects 0.000 description 3
- 238000000295 emission spectrum Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229920005604 random copolymer Polymers 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 238000012719 thermal polymerization Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 2
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 description 2
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
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- 239000002202 Polyethylene glycol Substances 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
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- 125000005250 alkyl acrylate group Chemical group 0.000 description 2
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- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 2
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- 238000012662 bulk polymerization Methods 0.000 description 2
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 2
- WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 2
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- ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000012766 organic filler Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
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Classifications
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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
- 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
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
-
- 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
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- 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
- C09J133/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
-
- 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
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/08—Homopolymers or copolymers of acrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2312/00—Crosslinking
- C08L2312/06—Crosslinking by radiation
-
- 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
- C09J2433/00—Presence of (meth)acrylic polymer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12193296.6A EP2733186A1 (en) | 2012-11-19 | 2012-11-19 | Highly tackified acrylate pressure sensitive adhesives |
| EP12193296.6 | 2012-11-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20150087293A true KR20150087293A (ko) | 2015-07-29 |
Family
ID=47215428
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020157015804A Ceased KR20150087293A (ko) | 2012-11-19 | 2013-11-05 | 고도로 점착부여된 아크릴레이트 감압 접착제 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US9701873B2 (OSRAM) |
| EP (2) | EP2733186A1 (OSRAM) |
| JP (1) | JP6469017B2 (OSRAM) |
| KR (1) | KR20150087293A (OSRAM) |
| CN (1) | CN104797671B (OSRAM) |
| WO (1) | WO2014078118A1 (OSRAM) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2021006593A1 (ko) * | 2019-07-11 | 2021-01-14 | (주)촌시스 | 기능성 핫멜트 점착제의 제조방법 및 그에 따른 기능성 핫멜트 점착제 |
| KR20220092727A (ko) * | 2020-12-24 | 2022-07-04 | (주)애니원 | 접착 시트, 접착 시트의 제조 방법 및 접착 시트를 이용한 접착층의 형성 방법 |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2733186A1 (en) * | 2012-11-19 | 2014-05-21 | 3M Innovative Properties Company | Highly tackified acrylate pressure sensitive adhesives |
| US20170362468A1 (en) * | 2014-12-22 | 2017-12-21 | 3M Innovative Properties Company | Tackified acrylate pressure sensitive adhesives with low acid content |
| WO2016133669A1 (en) * | 2015-02-18 | 2016-08-25 | 3M Innovative Properties Company | Acrylic adhesive composition from protected photocrosslinking agents |
| US10920116B2 (en) | 2015-04-13 | 2021-02-16 | 3M Innovative Properties Company | Method of preparing crosslinked pressure-sensitive adhesives using a light-emitting diode for crosslinking |
| CN107920923A (zh) * | 2015-08-31 | 2018-04-17 | 3M创新有限公司 | 包含对湿表面具有增强的粘附性的(甲基)丙烯酸酯压敏粘合剂的负压伤口治疗敷料 |
| JP2017193601A (ja) * | 2016-04-18 | 2017-10-26 | 綜研化学株式会社 | 光硬化型粘着剤前駆体組成物、光硬化型粘着剤、及び光硬化型粘着剤の製造方法 |
| WO2018005585A1 (en) * | 2016-06-29 | 2018-01-04 | 3M Innovative Properties Company | Ionizing radiation crosslinkable tackifed (meth)acrylate (co)polymer pressure sensitive adhesives with low acid content |
| EP3497174A4 (en) | 2016-08-10 | 2020-04-22 | 3M Innovative Properties Company | FLUORED PRESSURE SENSITIVE ADHESIVE |
| JP7055972B2 (ja) * | 2016-10-26 | 2022-04-19 | スリーエム イノベイティブ プロパティズ カンパニー | 架橋性組成物及び架橋された組成物 |
| WO2018090354A1 (zh) * | 2016-11-21 | 2018-05-24 | 北京英力科技发展有限公司 | 一种无苯释放的光固化组合物 |
| US11512152B2 (en) | 2017-02-27 | 2022-11-29 | Lg Chem, Ltd. | Method of preparing acrylic adhesive and adhesive film prepared therefrom |
| DE102017114256A1 (de) * | 2017-06-27 | 2018-12-27 | Certoplast Technische Klebebänder Gmbh | Verfahren zur Herstellung eines Klebebandes |
| DE102017114266B9 (de) * | 2017-06-27 | 2020-09-17 | Certoplast Technische Klebebänder Gmbh | Verfahren zur Herstellung eines Wickelbandes |
| JP7777984B2 (ja) * | 2018-12-27 | 2025-12-01 | ソルベンタム インテレクチュアル プロパティズ カンパニー | ホットメルト加工可能な（メタ）アクリレート系医療用接着剤 |
| CN114089603A (zh) * | 2020-08-24 | 2022-02-25 | 乐凯华光印刷科技有限公司 | 一种柔性版支持体及其制备方法和使用方法 |
| JP2022050067A (ja) * | 2020-09-17 | 2022-03-30 | 日東電工株式会社 | 画像表示装置に用いる粘着剤組成物、粘着剤層付き光学フィルム及び画像表示装置 |
| CN114163933A (zh) * | 2021-12-01 | 2022-03-11 | 安徽富印新材料有限公司 | 一种改性丙烯酸酯压敏胶及其制备方法 |
| CN114921191A (zh) * | 2022-01-28 | 2022-08-19 | 沧州临港弘达新材料制造有限公司 | 一种高性能环保辐射固化型热熔压敏胶粘剂及其制备方法 |
| JP2023127040A (ja) * | 2022-03-01 | 2023-09-13 | 三菱ケミカル株式会社 | 活性エネルギー線硬化性粘着剤組成物、およびそれを用いてなる粘着剤、粘着テープ |
| CN119630716A (zh) * | 2022-08-09 | 2025-03-14 | 大阪有机化学工业株式会社 | 光聚合引发剂组合物、光固化性组合物、光固化性组合物套组和光固化性树脂组合物 |
| CN120283025A (zh) * | 2022-12-21 | 2025-07-08 | 舒万诺知识产权公司 | 湿气可透过的可热熔加工的医疗粘合剂 |
| WO2024179886A1 (en) * | 2023-02-27 | 2024-09-06 | Basf Se | Uv-curable solvent-free hotmelt adhesive comprising a uv-crosslinkable poly(meth)acrylate and a radiation-curable, free-radically polymerizable compound |
| CN120752265A (zh) * | 2023-03-27 | 2025-10-03 | 三菱化学株式会社 | 树脂、糊剂组合物、无机烧结体、电子器件和太阳能板 |
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| US4181752A (en) | 1974-09-03 | 1980-01-01 | Minnesota Mining And Manufacturing Company | Acrylic-type pressure sensitive adhesives by means of ultraviolet radiation curing |
| US4330590A (en) | 1980-02-14 | 1982-05-18 | Minnesota Mining And Manufacturing Company | Photoactive mixture of acrylic monomers and chromophore-substituted halomethyl-2-triazine |
| US4379201A (en) | 1981-03-30 | 1983-04-05 | Minnesota Mining And Manufacturing Company | Multiacrylate cross-linking agents in pressure-sensitive photoadhesives |
| US4391678A (en) | 1981-11-18 | 1983-07-05 | The United States Of America As Represented By The Secretary Of The Army | Methods of making infrared detector array cold shield |
| US4602097A (en) | 1984-06-11 | 1986-07-22 | Ulano Corporation | Water soluble photoinitiator benzophenone and thioxanthenone ethoxy-ether derivatives |
| US4737559A (en) * | 1986-05-19 | 1988-04-12 | Minnesota Mining And Manufacturing Co. | Pressure-sensitive adhesive crosslinked by copolymerizable aromatic ketone monomers |
| CA2129730C (en) | 1992-02-10 | 1998-07-14 | Albert I. Everaerts | Radiation crosslinked elastomers |
| US5804610A (en) | 1994-09-09 | 1998-09-08 | Minnesota Mining And Manufacturing Company | Methods of making packaged viscoelastic compositions |
| WO1996035725A1 (en) | 1995-05-10 | 1996-11-14 | Avery Dennison Corporation | Pigmented, uv-cured, acrylic-based, pressure sensitive adhesives, and method for making same |
| JP2000509089A (ja) | 1996-04-19 | 2000-07-18 | ミネソタ・マイニング・アンド・マニュファクチャリング・カンパニー | ポリマを放射線架橋する方法及び放射線架橋性組成物 |
| DE10008842C1 (de) | 2000-02-25 | 2001-06-28 | Beiersdorf Ag | Polymerblends |
| EP2103297B1 (de) * | 2008-03-20 | 2012-05-16 | Ivoclar Vivadent AG | Polymerisierbare Zusammensetzung mit mehrere Germanium-Atome enthaltenden Initiatoren |
| JP4903914B2 (ja) | 2008-07-02 | 2012-03-28 | スリーエム イノベイティブ プロパティズ カンパニー | 低表面エネルギー接着剤 |
| US7838110B2 (en) * | 2008-12-02 | 2010-11-23 | 3M Innovative Properties Company | Aziridine-functional photoactive crosslinking compounds |
| DE102009007589A1 (de) | 2009-02-05 | 2010-08-12 | Tesa Se | Transfer-Haftklebeband sowie Verfahren zur Herstellung eines Haftklebebandes |
| US8791207B2 (en) | 2010-01-15 | 2014-07-29 | 3M Innovative Properties Company | Adhesive composition |
| CN103210048B (zh) | 2010-09-30 | 2016-03-16 | 3M创新有限公司 | 高度增粘、可热熔加工的丙烯酸酯压敏粘合剂 |
| EP2733186A1 (en) * | 2012-11-19 | 2014-05-21 | 3M Innovative Properties Company | Highly tackified acrylate pressure sensitive adhesives |
-
2012
- 2012-11-19 EP EP12193296.6A patent/EP2733186A1/en not_active Withdrawn
-
2013
- 2013-11-05 KR KR1020157015804A patent/KR20150087293A/ko not_active Ceased
- 2013-11-05 EP EP13792554.1A patent/EP2920264B1/en not_active Not-in-force
- 2013-11-05 US US14/442,874 patent/US9701873B2/en not_active Expired - Fee Related
- 2013-11-05 JP JP2015543096A patent/JP6469017B2/ja not_active Expired - Fee Related
- 2013-11-05 CN CN201380060473.4A patent/CN104797671B/zh not_active Expired - Fee Related
- 2013-11-05 WO PCT/US2013/068376 patent/WO2014078118A1/en not_active Ceased
-
2017
- 2017-07-10 US US15/644,970 patent/US10035931B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2021006593A1 (ko) * | 2019-07-11 | 2021-01-14 | (주)촌시스 | 기능성 핫멜트 점착제의 제조방법 및 그에 따른 기능성 핫멜트 점착제 |
| KR20220092727A (ko) * | 2020-12-24 | 2022-07-04 | (주)애니원 | 접착 시트, 접착 시트의 제조 방법 및 접착 시트를 이용한 접착층의 형성 방법 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2920264B1 (en) | 2018-12-26 |
| EP2920264A1 (en) | 2015-09-23 |
| US20150291853A1 (en) | 2015-10-15 |
| CN104797671B (zh) | 2018-03-27 |
| WO2014078118A1 (en) | 2014-05-22 |
| US20170313908A1 (en) | 2017-11-02 |
| US10035931B2 (en) | 2018-07-31 |
| JP6469017B2 (ja) | 2019-02-13 |
| CN104797671A (zh) | 2015-07-22 |
| EP2733186A1 (en) | 2014-05-21 |
| US9701873B2 (en) | 2017-07-11 |
| JP2016501290A (ja) | 2016-01-18 |
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