TWI630248B - 黏結膜用光固化樹脂組合物及黏結膜 - Google Patents
黏結膜用光固化樹脂組合物及黏結膜 Download PDFInfo
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- TWI630248B TWI630248B TW104109016A TW104109016A TWI630248B TW I630248 B TWI630248 B TW I630248B TW 104109016 A TW104109016 A TW 104109016A TW 104109016 A TW104109016 A TW 104109016A TW I630248 B TWI630248 B TW I630248B
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- meth
- acrylate
- photocurable resin
- resin composition
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- 239000011342 resin composition Substances 0.000 title claims abstract description 39
- 239000002313 adhesive film Substances 0.000 title description 10
- 239000012790 adhesive layer Substances 0.000 title 1
- 229920005989 resin Polymers 0.000 claims abstract description 29
- 239000011347 resin Substances 0.000 claims abstract description 29
- 239000003607 modifier Substances 0.000 claims abstract description 26
- 239000011230 binding agent Substances 0.000 claims abstract description 20
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 109
- 239000000178 monomer Substances 0.000 claims description 36
- -1 3-mercaptopropyloxy Chemical group 0.000 claims description 30
- 239000003999 initiator Substances 0.000 claims description 15
- 238000004132 cross linking Methods 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 8
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 238000000016 photochemical curing Methods 0.000 claims description 6
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 5
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- UOMUPDCRXJLVGR-UHFFFAOYSA-N propane-1,2,2-triol Chemical compound CC(O)(O)CO UOMUPDCRXJLVGR-UHFFFAOYSA-N 0.000 claims description 4
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims description 3
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 claims description 3
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 3
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 3
- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 claims description 3
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-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
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- 244000028419 Styrax benzoin Species 0.000 claims description 3
- 235000000126 Styrax benzoin Nutrition 0.000 claims description 3
- 235000008411 Sumatra benzointree Nutrition 0.000 claims description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 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 claims description 3
- 229960002130 benzoin Drugs 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 3
- VIBDJEWPNNCFQO-UHFFFAOYSA-N ethane-1,1,2-triol Chemical compound OCC(O)O VIBDJEWPNNCFQO-UHFFFAOYSA-N 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 235000019382 gum benzoic Nutrition 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
- 239000011976 maleic acid Substances 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- IMQFZQVZKBIPCQ-UHFFFAOYSA-N 2,2-bis(3-sulfanylpropanoyloxymethyl)butyl 3-sulfanylpropanoate Chemical compound SCCC(=O)OCC(CC)(COC(=O)CCS)COC(=O)CCS IMQFZQVZKBIPCQ-UHFFFAOYSA-N 0.000 claims description 2
- CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 claims description 2
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- XVQUOJBERHHONY-UHFFFAOYSA-N isometheptene Chemical group CNC(C)CCC=C(C)C XVQUOJBERHHONY-UHFFFAOYSA-N 0.000 claims description 2
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims description 2
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 claims description 2
- 235000019260 propionic acid Nutrition 0.000 claims description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 2
- VLCCKNLIFIJYOQ-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] 2,2,3,3-tetrakis(sulfanyl)propanoate Chemical compound OCC(CO)(CO)COC(=O)C(S)(S)C(S)S VLCCKNLIFIJYOQ-UHFFFAOYSA-N 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 238000007711 solidification Methods 0.000 claims 1
- 230000008023 solidification Effects 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000001723 curing Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
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- 210000000795 conjunctiva Anatomy 0.000 description 2
- 238000005034 decoration Methods 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 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 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- XQLGJSOZVUDHCP-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;2,2,3,3-tetrakis(sulfanyl)propanoic acid Chemical compound OCC(CO)(CO)CO.OC(=O)C(S)(S)C(S)S XQLGJSOZVUDHCP-UHFFFAOYSA-N 0.000 description 1
- JGRXEBOFWPLEAV-UHFFFAOYSA-N 2-ethylbutyl prop-2-enoate Chemical compound CCC(CC)COC(=O)C=C JGRXEBOFWPLEAV-UHFFFAOYSA-N 0.000 description 1
- 102100027123 55 kDa erythrocyte membrane protein Human genes 0.000 description 1
- 101001057956 Homo sapiens 55 kDa erythrocyte membrane protein Proteins 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- LLUQGQGBJGTOSP-UHFFFAOYSA-N SC(C(C(=O)OCC(CO)(CO)CO)(S)S)(C)S Chemical compound SC(C(C(=O)OCC(CO)(CO)CO)(S)S)(C)S LLUQGQGBJGTOSP-UHFFFAOYSA-N 0.000 description 1
- MRXRIKVEVBFHJU-UHFFFAOYSA-N SCCC(=O)O.SCCC(=O)O.SCCC(=O)O.C(O)C(CC)(CO)CO.SCCC(=O)O.SCCC(=O)O.SCCC(=O)O Chemical compound SCCC(=O)O.SCCC(=O)O.SCCC(=O)O.C(O)C(CC)(CO)CO.SCCC(=O)O.SCCC(=O)O.SCCC(=O)O MRXRIKVEVBFHJU-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
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- 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
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/12—Esters of monohydric alcohols or phenols
- C08F20/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F20/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
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- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
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- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
- C08L33/12—Homopolymers or copolymers of methyl methacrylate
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- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
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- 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
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- 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
- C09J133/10—Homopolymers or copolymers of methacrylic acid esters
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- C—CHEMISTRY; METALLURGY
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Abstract
本發明是關於一種包含由多官能分子量調節劑封端及交聯之(甲基)丙烯酸酯((meth)acrylic acid ester)類光固化樹脂的黏結膜用光固化樹脂組合物。
Description
本發明是關於一種黏結膜用光固化樹脂組合物及黏結膜。
黏結膜廣泛地應用於電子產品的部件間之結合、室內裝飾用廚房傢俱、廚櫃或傢俱等的內置用品或汽車內置及外置材料的黏結用。
本發明的一實施例提供一種可製備耐久性得到提高之黏結膜的光固化樹脂組合物。
本發明的另一實施例提供一種由該光固化樹脂組合物製備的黏結膜。
本發明的一實施例提供一種包含由多官能分子量調節劑封端(end-capping)及交聯的(甲基)丙烯酸酯((meth)acrylic acid ester)類光固化樹脂的黏結膜用光固化樹脂組合物。
在本發明的一實施例中，該(甲基)丙烯酸酯類光固化樹脂的重均分子量可以為3000000至15000000。
在本發明的一實施例中，該多官能分子量調節劑可以為二官能度以上。
在本發明的一實施例中，該多官能分子量調節劑可以為三官能度至六官能度的含有硫醇基(thiol group)之化合物。
在本發明的-實施例中，該多官能分子量調節劑可包含選自由三-[(3-巰基丙醯氧基)-乙基]異氰脲酸酯(tris-[(3-mercapto-propionyloxy)-ethyl]isocyanurate)、三羥甲基丙烷三(3-巰基丙酸酯)(trimethylolpropane
tris(3-mercaptopropionate)、季戊四醇四-3-巰基丙酸酯(pentaerythritol-tetrakis-3-mercaptopropionate)、二季戊四醇六-3-巰基丙酸酯(dipentaerythritol hexa-3-mercaptopropionate)、季戊四醇四-3-巰基丁酸酯(pentaerythritol-tetrakis-3-mercaptobutyrate)及其組合中的至少一種。
在本發明的一實施例中，該(甲基)丙烯酸酯類光固化樹脂能夠以100重量份的(甲基)丙烯酸酯類單體及0.001至1.0重量份的多官能分子量調節劑的含量比混合而進行聚合。
在本發明的一實施例中，該(甲基)丙烯酸酯類單體可以為包含選自由(甲基)丙烯酸甲酯(methyl(meth)acrylate)、(甲基)丙烯酸乙酯(ethyl(meth)acrylate)、(甲基)丙烯酸正丙酯(n-propyl(meth)acrylate)、(甲基)丙烯酸異丙酯(isopropyl(meth)acrylate)、(甲基)丙烯酸正丁酯(n-butyl(meth)acrylate)、(甲基)丙烯酸叔丁酯(t-butyl(meth)acrylate)、(甲基)丙烯酸仲丁酯(sec-butyl(meth)acrylate)、(甲基)丙烯酸戊酯(pentyl(meth)acrylate)、(甲基)丙烯酸2-乙基己酯(2-ethylhexyl(meth)acrylate)、(甲基)丙烯酸2-乙基丁酯(2-ethyl-butyl(meth)acrylate)、(甲基)丙烯酸正辛酯(n-octyl(meth)acrylate)、(甲基)丙烯酸異辛酯(isooctyl(meth)acrylate)、(甲基)丙烯酸異冰片酯(isobornyl (meth)acrylate)、(甲基)丙烯酸異壬酯(isononyl(meth)acrylate)及其組合所組成之群組中的一種的丙烯酸類光固化樹脂組合物或環氧丙烯酸酯類光固化樹脂組合物的固化物。
在本發明的一實施例中，該(甲基)丙烯酸酯類光固化樹脂可由該(甲基)丙烯酸酯類單體和包含選自由含有羥基(hydroxy group)的單體、含有羧基(carboxyl group)的單體或含有氮的單體及其組合所組成之群組中的至少一種的交聯單體一同進行共聚合。
在本發明的一實施例中，該交聯單體可包含選自由2-羥基乙基(甲基)丙烯酸酯(2-hydroxyethyl(meth)acrylate)、2-羥基丙基(甲基)丙烯酸酯(2-hydroxypropyl(meth)acrylate)、4-羥基丁基(甲基)丙烯酸酯(4-hydroxybutyl(meth)acrylate)、6-羥基己基(甲基)丙烯酸酯(6-hydroxyhexyl(meth)acrylate)、8-羥基辛基(甲基)丙烯酸酯
(8-hydroxyoctyl(meth)acrylate)、2-羥基乙二醇(甲基)丙烯酸酯(2-hydroxy ethylene glycol(meth)acrylate)、2-羥基丙二醇(甲基)丙烯酸酯(2-hydroxy propylene glycol(meth)acrylate)、丙烯酸(acrylic acid)、甲基丙烯酸(methcrylic acid)、2-(甲基)丙烯醯氧基乙酸(2-(meth)acryloyloxy acetic acid)、3-(甲基)丙烯醯氧基丙酸(3-(meth)acryloyloxy propanoic acid)、4-(甲基)丙烯醯氧基丁酸(4-(meth)acryloyloxy-butyric acid)、丙烯酸(acrylic acid)二聚體、衣康酸(itaconic acid)、馬來酸(maleic acid)、2-異氰酸根合乙基(甲基)丙烯酸酯(2-isocyanato ethyl(meth)acrylate)、3-異氰酸丙基(甲基)丙烯酸酯(3-isocyanato propyl(meth)acrylate)、4-異氰酸根合丁基(甲基)丙烯酸酯(4-isocyanato-butyl(meth)acrylate)、(甲基)丙烯醯胺((meth)acrylamide)、N-乙烯基吡咯烷酮(N-vinylpyrrolidone)、N-乙烯基己內醯胺(N-vinyl caprolactam)及其組合所組成之群組中的一種。
在本發明的一實施例中，該黏結膜用光固化樹脂組合物更可包含光引發劑。
在本發明的一實施例中，該光引發劑可包含選自由安息香(benzoin)類引發劑、羥基酮(hydroxyketone)類引發劑、氨基酮(aminoketone)類引發劑、己內醯胺(caprolactam)類引發劑及其組合所組成之群組中的一種。
本發明的另一實施例提供一種包含該黏結膜用光固化樹脂組合物之光固化物的黏結膜。
上述光固化樹脂組合物能夠製備耐久性得到改善的黏結膜。
以下，對本發明的實施例進行詳細說明。但這僅作為例示而提出，本發明並不局限於此，本發明僅根據後述的申請專利範圍來定義。
本發明的一實施例提供一種包含由多官能分子量調節劑封
端及交聯之(甲基)丙烯酸酯類光固化樹脂的黏結膜用光固化樹脂組合物。
該(甲基)丙烯酸酯類光固化樹脂在合成樹脂時使用該多官能分子量調節劑來製備，從而具有規定的數值範圍之分子量，以用於該光固化樹脂組合物。
例如，該(甲基)丙烯酸酯類光固化樹脂的重均分子量可以為約3000000至約15000000。黏結膜用光固化樹脂組合物藉由包含重均分子量為約3000000至約15000000的高分子量的(甲基)丙烯酸酯類光固化樹脂，可提高由該黏結膜用光固化樹脂組合物製備的黏結膜之耐久性。
該多官能分子量調節劑在封端該(甲基)丙烯酸酯類光固化樹脂後，可由該多官能分子量調節劑的未反應官能團在該光固化樹脂組合物進行光固化時執行額外的交聯劑作用。其結果，在該光固化樹脂組合物進行光固化後，其固化物可形成三維交聯結構，並且，能夠更加提高固化密度。
若該光固化樹脂組合物之光固化物的固化密度變高，則提高耐久性，尤其，提高高溫物性，例如，提高高溫剪切強度之類的物性值。
該多官能分子量調節劑可以為二官能度以上，具體地，可以為三官能度至六官能度的含有硫醇基之化合物。
當合成該(甲基)丙烯酸酯類光固化樹脂時，若不使用該多官能分子量調節劑，而使用一官能分子量調節劑，則未反應的一官能分子量調節劑繼續殘留在黏結膜用光固化樹脂組合物內，從而不能執行交聯作用，而執行光固化時縮短固化物的鏈結構之作用，因此成為減少該(甲基)丙烯酸酯類光固化樹脂的光固化物之分子量的原因，其結果，有可能降低耐久性。
與此相反，在二官能度以上的多官能分子量調節劑的情況下，調節高分子鏈長度的作用比一官能的情況差，但隨著在該光固化樹脂組合物內進行聚合或固化時作用為交聯劑，反而提高聚合物或固化物的分子量。具體地，即使該多官能分子量調節劑內的兩種以上之官能團中的一種與單體發生反應，並與單體或聚合物末端相連接，該多官能分子量調節劑也仍然殘留有一種以上的官能團，因而剩下的一種以上的官能團可與另
一單體或聚合物重新發生反應，從而執行交聯作用。若該多官能分子量調節劑只有一種官能團，則與單體或聚合物末端相連接，來僅執行封端作用，從而執行斷開聚合反應的鏈之作用。
若該多官能分子量調節劑為三官能度至六官能度的含有硫醇基之化合物，則硫醇基與該(甲基)丙烯酸酯類光固化樹脂的雙鍵發生反應，從而可作用為交聯劑。
例如，該多官能分子量調節劑可以為三-[(3-巰基丙醯氧基)-乙基]異氰脲酸酯、三羥甲基丙烷三(3-巰基丙酸酯)、季戊四醇四-3-巰基丙酸酯、二季戊四醇六-3-巰基丙酸酯、季戊四醇四-3-巰基丁酸酯等，亦可包含它們的組合。
為了製備該黏結膜用光固化樹脂組合物，製備預先由該多官能分子量調節劑封端的(甲基)丙烯酸酯類光固化樹脂。該(甲基)丙烯酸酯類光固化樹脂能夠以100重量份的(甲基)丙烯酸酯類單體及約0.001至約1.0重量份的多官能分子量調節劑的含量比混合而進行聚合。
當聚合該(甲基)丙烯酸酯類光固化樹脂時，以上述含量比使用多官能分子量調節劑，可合成具有所需程度之分子量的樹脂，當以超過上述含量範圍的方式使用過量時，會發生硫醇基之間的副反應，從而具有樹脂的純度有可能下降的擔憂。
例如，該(甲基)丙烯酸酯類單體可以為(甲基)丙烯酸烷基酯(alkyl(meth)acrylate)，但本發明並不局限於此。該(甲基)丙烯酸烷基酯的烷基可以為線性或分支型C1-C14烷基，具體可以為C1-C8烷基。
具體地，該(甲基)丙烯酸酯類單體可包含選自由(甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸正丙酯、(甲基)丙烯酸異丙酯、(甲基)丙烯酸正丁酯、(甲基)丙烯酸叔丁酯、(甲基)丙烯酸仲丁酯、(甲基)丙烯酸戊酯、(甲基)丙烯酸2-乙基己酯、(甲基)丙烯酸2-乙基丁酯、(甲基)丙烯酸正辛酯、(甲基)丙烯酸異辛酯、(甲基)丙烯酸異冰片酯、(甲基)丙烯酸異壬酯及其組合所組成之群組中的一種。
該(甲基)丙烯酸酯類光固化樹脂可由該(甲基)丙烯酸酯
類單體和交聯單體一同進行共聚合。
該交聯單體意味著在分子結構內同時包含共聚合性官能團(例如，碳-碳雙鍵)及交聯性官能團的單體。
例如，該交聯單體可包含選自由含有羥基的單體、含有羧基的單體或含有氮的單體及其組合所組成之群組中的一種，但本發明並不局限於此。
具體地，該交聯單體可包含選自由2-羥基乙基(甲基)丙烯酸酯、2-羥基丙基(甲基)丙烯酸酯、4-羥基丁基(甲基)丙烯酸酯、6-羥基己基(甲基)丙烯酸酯、8-羥基辛基(甲基)丙烯酸酯、2-羥基乙二醇(甲基)丙烯酸酯、2-羥基丙二醇(甲基)丙烯酸酯等之類的含有羥基的單體、丙烯酸、甲基丙烯酸、2-(甲基)丙烯醯氧基乙酸、3-(甲基)丙烯醯氧基丙酸、4-(甲基)丙烯醯氧基丁酸、丙烯酸二聚體、衣康酸、馬來酸等之類的含有羧基的單體、2-異氰酸根合乙基(甲基)丙烯酸酯、3-異氰酸丙基(甲基)丙烯酸酯、4-異氰酸根合丁基(甲基)丙烯酸酯、(甲基)丙烯醯胺、N-乙烯基吡咯烷酮、N-乙烯基己內醯胺等之類的含有氮的單體及其組合所組成之群組中的一種。
該黏結膜用光固化樹脂組合物為了由光固化性組合物調節聚合度，更可包含光引發劑。相對於100重量份的該(甲基)丙烯酸酯類光固化樹脂，可使用約0.01至約10重量份含量的該光引發劑，作為該光引發劑的種類，只要是可藉由光照射來產生自由基，從而引發聚合反應，那麼就不受特別的限制，例如，可包含選自由安息香類引發劑、羥基酮類引發劑、氨基酮類引發劑、己內醯胺類引發劑及其組合所組成之群組中的一種。
並且，在不影響發明效果的範圍內，該黏結膜用光固化樹脂組合物更可包含選自由環氧樹脂、交聯劑、紫外線穩定劑、抗氧化劑、調色劑、加固劑、填充劑、消泡劑、表面活性劑、增塑劑及其組合所組成之群組中的至少一種添加劑。
本發明的另一實施例提供一種包含該黏結膜用光固化樹脂組合物之光固化物的黏結膜。
該黏結膜能夠以多種用途廣泛地應用於電子產品的部件之間的結合、室內裝飾用廚房傢俱、廚櫃或傢俱等的內置用品或汽車內置及外置材料的黏結用等，且耐久性優異。
在本發明的一實施例中，該黏結膜是在將該黏結膜用光固化樹脂組合物塗敷於基材上後，進行光固化來成膜的黏結膜。例如，可由基材在離型膜上形成黏結膜，當在具體用途中適用黏結膜時，可除去離型膜來使用黏結膜。
如前所述，該黏結膜因使用具有高分子量的(甲基)丙烯酸酯類光固化樹脂來製備，因而耐久性優異。
以下，記載本發明的實施例及比較例。這種以下實施例只是本發明的一實施例，本發明並不局限於以下實施例。
實施例
實施例1
在1公升的玻璃反應器中放入91重量份的2-EHA(2-丙烯酸乙基己酯(2-ethylhexyl acrylate))、9重量份的作為交聯單體之丙烯酸及0.005重量份的作為光聚合引發劑之1-羥基環己基苯基甲酮(1-hydroxycyclohexyl phenyl ketone)(豔佳固(Irgacure)184，巴斯夫(BASF)公司)，添加0.005重量份的季戊四醇四-3-巰基丙酸酯(PEMP，SC有機化學)作為多官能分子量調節劑並進行混合後，利用氮氣來淨化30分鐘，從而使溶液內部的氣體取代為氮氣。利用黑色螢光燈來照射紫外線(UV)，從而將(甲基)丙烯酸酯類光固化樹脂進行光聚合。使用凝膠滲透色譜儀(GPC)(1260 Infinity，安捷倫(Agilent)公司)來測定所聚合的(甲基)丙烯酸酯類光固化樹脂的重均分子量及多分散性指數(PDI)，並在下表1中記載了所測定的重均分子量及多分散性指數值。
在合成的該(甲基)丙烯酸酯類光固化樹脂中混合光引發劑、固化劑及其他添加劑來製備光固化樹脂組合物，並在聚對苯二甲酸乙二醇酯(PET，polyethylene terephthalate)離型膜上塗敷該光固化樹脂組合物後，利用紫外燈來照射紫外線10分鐘，並進行光固化，從而製備了黏結膜。
比較例1
除了使用正十二烷基硫醇(n-DDM，n-dodecyl mercaptan)作為分子量調節劑之外，以與實施例1相同的方法製備了光固化樹脂組合物，並以相同的方法製備了黏結膜。
評價
測定高溫動態剪切強度(Dynamic shear strength)
相對於實施例1及比較例1的黏結帶，在以使黏結帶與不銹鋼(SUS)板和不銹鋼板之間相接的方式層疊之後，利用6kg的載荷來加壓30秒鐘後，在常溫條件下時效處理(aging)15分鐘，並進行附著。然後，利用具有維持80℃的高溫之腔室的萬能試驗機(UTM，universal testing machine)，在80℃溫度下，藉由以1.0mm/min的速度(cross head speed)拉動基材的兩側，從而測定了高溫動態剪切強度。
從上述表1的結果可以確認到由於實施例1的剪切強度優異於比較例1，從而耐久性優異。
雖然本發明已用較佳實施例揭露如上，然其並非用以限定本發明，本發明所屬技術領域中具有通常知識者，在不脫離本發明之精神和範圍內，當可作各種之更動與潤飾，因此本發明之保護範圍當視後附之申請專利範圍所界定者為準。
Claims (9)
- 一種黏結膜用光固化樹脂組合物，包含由多官能分子量調節劑封端(end-capping)及交聯的(甲基)丙烯酸酯((meth)acrylic acid ester)類光固化樹脂，其中該(甲基)丙烯酸酯類光固化樹脂以100重量份的(甲基)丙烯酸酯類單體及0.001至1.0重量份的多官能分子量調節劑的含量比混合而進行聚合，其中該(甲基)丙烯酸酯類光固化樹脂的重均分子量為1700000至15000000。
- 如申請專利範圍第1項所述之黏結膜用光固化樹脂組合物，其中該多官能分子量調節劑為二官能度至六官能度的含有硫醇基(thiol group)之化合物。
- 如申請專利範圍第1項所述之黏結膜用光固化樹脂組合物，其中該多官能分子量調節劑包含選自由三-[(3-巰基丙醯氧基)-乙基]異氰脲酸酯(tris-[(3-mercapto-propionyloxy)-ethyl]isocyanurate)、三羥甲基丙烷三(3-巰基丙酸酯)(trimethylolpropane tris(3-mercaptopropionate)、季戊四醇四-3-巰基丙酸酯(pentaerythritol-tetrakis-3-mercaptopropionate)、二季戊四醇六-3-巰基丙酸酯(dipentaerythritol hexa-3-mercaptopropionate)及季戊四醇四-3-巰基丁酸酯(pentaerythritol-tetrakis-3-mercaptobutyrate)中的至少一種。
- 如申請專利範圍第1項所述之黏結膜用光固化樹脂組合物，其中該(甲基)丙烯酸酯類單體為包含選自由(甲基)丙烯酸甲酯(methyl(meth)acrylate)、(甲基)丙烯酸乙酯(ethyl(meth)acrylate)、(甲基)丙烯酸正丙酯(n-propyl(meth)acrylate)、(甲基)丙烯酸異丙酯(isopropyl(meth)acrylate)、(甲基)丙烯酸正丁酯(n-butyl(meth)acrylate)、(甲基)丙烯酸叔丁酯(t-butyl(meth)acrylate)、(甲基)丙烯酸仲丁酯(sec-butyl(meth)acrylate)、(甲基)丙烯酸戊酯(pentyl(meth)acrylate)、(甲基)丙烯酸2-乙基己酯(2-ethylhexyl(meth)acrylate)、(甲基)丙烯酸2-乙基丁酯(2-ethyl-butyl(meth)acrylate)、(甲基)丙烯酸正辛酯(n-octyl(meth)acrylate)、(甲基)丙烯酸異辛酯(isooctyl(meth)acrylate)、(甲基)丙烯酸異冰片酯(isobornyl(meth)acrylate)及(甲基)丙烯酸異壬酯(isononyl(meth)acrylate)所組成之群組中的一種的丙烯酸類光固化樹脂組合物或環氧丙烯酸酯類光固化樹脂組合物的固化物。
- 如申請專利範圍第1項所述之黏結膜用光固化樹脂組合物，其中該(甲基)丙烯酸酯類光固化樹脂由該(甲基)丙烯酸酯類單體和包含選自由含有羥基(hydroxy group)的單體、含有羧基(carboxyl group)的單體或含有氮的單體及其組合所組成之群組中的至少一種的交聯單體一同進行共聚合。
- 如申請專利範圍第5項所述之黏結膜用光固化樹脂組合物，其中該交聯單體包含選自由2-羥基乙基(甲基)丙烯酸酯(2-hydroxyethyl(meth)acrylate)、2-羥基丙基(甲基)丙烯酸酯(2-hydroxypropyl(meth)acrylate)、4-羥基丁基(甲基)丙烯酸酯(4-hydroxybutyl(meth)acrylate)、6-羥基己基(甲基)丙烯酸酯(6-hydroxyhexyl(meth)acrylate)、8-羥基辛基(甲基)丙烯酸酯(8-hydroxyoctyl(meth)acrylate)、2-羥基乙二醇(甲基)丙烯酸酯(2-hydroxy ethylene glycol(meth)acrylate)、2-羥基丙二醇(甲基)丙烯酸酯(2-hydroxy propylene glycol(meth)acrylate)、丙烯酸(acrylic acid)、甲基丙烯酸(methcrylic acid)、2-(甲基)丙烯醯氧基乙酸(2-(meth)acryloyloxy acetic acid)、3-(甲基)丙烯醯氧基丙酸(3-(meth)acryloyloxy propanoic acid)、4-(甲基)丙烯醯氧基丁酸(4-(meth)acryloyloxy-butyric acid)、丙烯酸(acrylic acid)二聚體、衣康酸(itaconic acid)、馬來酸(maleic acid)、2-異氰酸根合乙基(甲基)丙烯酸酯(2-isocyanato ethyl(meth)acrylate)、3-異氰酸丙基(甲基)丙烯酸酯(3-isocyanato propyl(meth)acrylate)、4-異氰酸根合丁基(甲基)丙烯酸酯(4-isocyanato-butyl(meth)acrylate)、(甲基)丙烯醯胺((meth)acrylamide)、N-乙烯基吡咯烷酮(N-vinylpyrrolidone)及N-乙烯基己內醯胺(N-vinyl caprolactam)所組成之群組中的一種。
- 如申請專利範圍第1項所述之黏結膜用光固化樹脂組合物，其中更包含光引發劑。
- 如申請專利範圍第7項所述之黏結膜用光固化樹脂組合物，其中該光引發劑包含選自由安息香(benzoin)類引發劑、羥基酮(hydroxyketone)類引發劑、氨基酮(aminoketone)類引發劑及己內醯胺(caprolactam)類引發劑所組成之群組中的一種。
- 一種黏結膜，包含如申請專利範圍第1至8項中任一項所述之黏結膜用光固化樹脂組合物的光固化物。
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