JP2007523227A - 接着剤 - Google Patents
接着剤 Download PDFInfo
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- JP2007523227A JP2007523227A JP2006548304A JP2006548304A JP2007523227A JP 2007523227 A JP2007523227 A JP 2007523227A JP 2006548304 A JP2006548304 A JP 2006548304A JP 2006548304 A JP2006548304 A JP 2006548304A JP 2007523227 A JP2007523227 A JP 2007523227A
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- Prior art keywords
- polymer
- polyols
- derived
- acrylate
- meth
- Prior art date
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- 230000001070 adhesive effect Effects 0.000 title claims description 57
- 239000000853 adhesive Substances 0.000 title claims description 56
- 229920000642 polymer Polymers 0.000 claims abstract description 114
- 229920005862 polyol Polymers 0.000 claims abstract description 76
- 239000000203 mixture Substances 0.000 claims abstract description 72
- 150000003077 polyols Chemical class 0.000 claims abstract description 57
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 43
- 229920001971 elastomer Polymers 0.000 claims abstract description 26
- 239000005060 rubber Substances 0.000 claims abstract description 24
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 23
- 238000000034 method Methods 0.000 claims abstract description 23
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 29
- 230000005855 radiation Effects 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 239000002243 precursor Substances 0.000 claims description 17
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 16
- 125000000962 organic group Chemical group 0.000 claims description 16
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 15
- 239000005062 Polybutadiene Substances 0.000 claims description 12
- 238000005227 gel permeation chromatography Methods 0.000 claims description 12
- 229920002857 polybutadiene Polymers 0.000 claims description 12
- 229920001577 copolymer Polymers 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 125000000524 functional group Chemical group 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 230000001588 bifunctional effect Effects 0.000 claims description 6
- 229920001400 block copolymer Polymers 0.000 claims description 6
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 125000000743 hydrocarbylene group Chemical group 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 4
- 125000002723 alicyclic group Chemical group 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 229920006158 high molecular weight polymer Polymers 0.000 claims description 3
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 230000002209 hydrophobic effect Effects 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 239000012939 laminating adhesive Substances 0.000 abstract description 8
- 239000004820 Pressure-sensitive adhesive Substances 0.000 abstract description 7
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- -1 acryl Chemical group 0.000 description 55
- 238000009472 formulation Methods 0.000 description 28
- 239000000178 monomer Substances 0.000 description 24
- 239000012948 isocyanate Substances 0.000 description 22
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- 150000002513 isocyanates Chemical class 0.000 description 17
- 238000006243 chemical reaction Methods 0.000 description 16
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- 125000001424 substituent group Chemical group 0.000 description 15
- 238000012360 testing method Methods 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 14
- 125000003118 aryl group Chemical group 0.000 description 12
- 239000007788 liquid Substances 0.000 description 12
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- 229920002635 polyurethane Polymers 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- 239000000758 substrate Substances 0.000 description 11
- 239000002253 acid Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 10
- 150000002148 esters Chemical class 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 229920000728 polyester Polymers 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical class C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 7
- 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 7
- 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 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 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 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 230000008859 change Effects 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 6
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 6
- PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 description 6
- 239000005056 polyisocyanate Substances 0.000 description 6
- 229920001228 polyisocyanate Polymers 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000005058 Isophorone diisocyanate Substances 0.000 description 5
- 229920002633 Kraton (polymer) Polymers 0.000 description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 5
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 5
- 125000002843 carboxylic acid group Chemical group 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 230000009477 glass transition Effects 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 230000007246 mechanism Effects 0.000 description 5
- 229920005903 polyol mixture Polymers 0.000 description 5
- 229920000909 polytetrahydrofuran Polymers 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 5
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- 239000002313 adhesive film Substances 0.000 description 4
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 238000001723 curing Methods 0.000 description 4
- 238000010894 electron beam technology Methods 0.000 description 4
- 230000000977 initiatory effect Effects 0.000 description 4
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 241000894007 species Species 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000007429 general method Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 125000005842 heteroatom Chemical group 0.000 description 3
- 239000012943 hotmelt Substances 0.000 description 3
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- 230000007062 hydrolysis Effects 0.000 description 3
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- 239000003999 initiator Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 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 2
- AZYRZNIYJDKRHO-UHFFFAOYSA-N 1,3-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC(C(C)(C)N=C=O)=C1 AZYRZNIYJDKRHO-UHFFFAOYSA-N 0.000 description 2
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 2
- HBKBEZURJSNABK-MWJPAGEPSA-N 2,3-dihydroxypropyl (1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(=O)OCC(O)CO HBKBEZURJSNABK-MWJPAGEPSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 238000003848 UV Light-Curing Methods 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
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- 238000007792 addition Methods 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
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- KSRVPHHTDYFCDN-UHFFFAOYSA-N 1,2,3-triphenyl-4-(2-phenylethenyl)benzene Chemical compound C=1C=CC=CC=1C=CC(C(=C1C=2C=CC=CC=2)C=2C=CC=CC=2)=CC=C1C1=CC=CC=C1 KSRVPHHTDYFCDN-UHFFFAOYSA-N 0.000 description 1
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
- XSCLFFBWRKTMTE-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)cyclohexane Chemical compound O=C=NCC1CCCC(CN=C=O)C1 XSCLFFBWRKTMTE-UHFFFAOYSA-N 0.000 description 1
- FVVSZDOJPYHTIK-UHFFFAOYSA-N 1,5-dibromo-2,4-diisocyanatobenzene Chemical compound BrC1=CC(Br)=C(N=C=O)C=C1N=C=O FVVSZDOJPYHTIK-UHFFFAOYSA-N 0.000 description 1
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 description 1
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- LFSYUSUFCBOHGU-UHFFFAOYSA-N 1-isocyanato-2-[(4-isocyanatophenyl)methyl]benzene Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=CC=C1N=C=O LFSYUSUFCBOHGU-UHFFFAOYSA-N 0.000 description 1
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 description 1
- OJRJDENLRJHEJO-UHFFFAOYSA-N 2,4-diethylpentane-1,5-diol Chemical compound CCC(CO)CC(CC)CO OJRJDENLRJHEJO-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
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
- NCTBYWFEJFTVEL-UHFFFAOYSA-N 2-methylbutyl prop-2-enoate Chemical compound CCC(C)COC(=O)C=C NCTBYWFEJFTVEL-UHFFFAOYSA-N 0.000 description 1
- QZWKEPYTBWZJJA-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine-4,4'-diisocyanate Chemical compound C1=C(N=C=O)C(OC)=CC(C=2C=C(OC)C(N=C=O)=CC=2)=C1 QZWKEPYTBWZJJA-UHFFFAOYSA-N 0.000 description 1
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- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
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- 0 C*OC(N*NC(O*OC(C1C(*)C1)=O)=O)=O Chemical compound C*OC(N*NC(O*OC(C1C(*)C1)=O)=O)=O 0.000 description 1
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- QXKRDKPTPNVQID-UHFFFAOYSA-N CONC(C=C1)=CC=C1C(C=C1)=CC=C1NOC.N=C=O.N=C=O Chemical compound CONC(C=C1)=CC=C1C(C=C1)=CC=C1NOC.N=C=O.N=C=O QXKRDKPTPNVQID-UHFFFAOYSA-N 0.000 description 1
- VOWAEIGWURALJQ-UHFFFAOYSA-N Dicyclohexyl phthalate Chemical compound C=1C=CC=C(C(=O)OC2CCCCC2)C=1C(=O)OC1CCCCC1 VOWAEIGWURALJQ-UHFFFAOYSA-N 0.000 description 1
- 229920001875 Ebonite Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/69—Polymers of conjugated dienes
- C08G18/698—Mixtures with compounds of group C08G18/40
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/751—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
- C08G18/752—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
- C08G18/753—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
- C08G18/755—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
- C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
-
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
-
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C09J175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2170/00—Compositions for adhesives
- C08G2170/40—Compositions for pressure-sensitive adhesives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2190/00—Compositions for sealing or packing joints
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polyurethanes Or Polyureas (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US53626004P | 2004-01-14 | 2004-01-14 | |
| PCT/EP2005/050046 WO2005068529A1 (en) | 2004-01-14 | 2005-01-06 | Adhesives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007523227A true JP2007523227A (ja) | 2007-08-16 |
| JP2007523227A5 JP2007523227A5 (https=) | 2010-05-06 |
Family
ID=34794395
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006548304A Pending JP2007523227A (ja) | 2004-01-14 | 2005-01-06 | 接着剤 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20070179254A1 (https=) |
| EP (1) | EP1706440A1 (https=) |
| JP (1) | JP2007523227A (https=) |
| KR (1) | KR20060122919A (https=) |
| CN (1) | CN1910215B (https=) |
| WO (1) | WO2005068529A1 (https=) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2011508057A (ja) * | 2007-12-27 | 2011-03-10 | スリーエム イノベイティブ プロパティズ カンパニー | 尿素系感圧性接着剤 |
| JP2011162770A (ja) * | 2010-01-15 | 2011-08-25 | Toyo Ink Sc Holdings Co Ltd | 活性エネルギー線硬化型接着剤 |
| JP2012526894A (ja) * | 2009-05-15 | 2012-11-01 | スリーエム イノベイティブ プロパティズ カンパニー | ウレタン系感圧接着剤 |
| WO2012165201A1 (ja) * | 2011-06-02 | 2012-12-06 | 株式会社きもと | 易剥離性粘着フィルム |
| JP2013532244A (ja) * | 2010-06-29 | 2013-08-15 | スリーエム イノベイティブ プロパティズ カンパニー | 窓フィルムの適用方法 |
| JP2013166877A (ja) * | 2012-02-16 | 2013-08-29 | Nitto Denko Corp | 放射線硬化型粘着剤組成物の製造方法、該製造方法で得られた放射線硬化型粘着剤組成物、および、該粘着剤組成物を用いた粘着シート |
| JP2013539493A (ja) * | 2010-08-26 | 2013-10-24 | スリーエム イノベイティブ プロパティズ カンパニー | 多層状両面接着剤 |
| JP2014210902A (ja) * | 2013-04-22 | 2014-11-13 | Dic株式会社 | 紫外線硬化型粘着剤組成物及び粘着剤 |
| JP2015003519A (ja) * | 2013-01-23 | 2015-01-08 | デクセリアルズ株式会社 | 親水性積層体、及びその製造方法、防汚用積層体、物品、及びその製造方法、並びに防汚方法 |
| JP2017521505A (ja) * | 2014-05-08 | 2017-08-03 | アルケマ フランス | 硬化性ウレタン(メタ)アクリレートポリマー組成物および方法 |
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| JP2013521195A (ja) | 2010-02-26 | 2013-06-10 | クラフト・フーヅ・グローバル・ブランヅ リミテッド ライアビリティ カンパニー | 接着剤ベースの再閉鎖可能な留め具を有するパッケージおよびそのための方法 |
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| CA2823068A1 (en) * | 2010-12-27 | 2012-07-05 | 3M Innovative Properties Company | Gel sealing corrosion prevention tape |
| CN103975033B (zh) * | 2011-12-07 | 2016-04-13 | 第一毛织株式会社 | 光固化粘合剂组合物以及包含它的显示装置 |
| JP6073081B2 (ja) * | 2012-07-12 | 2017-02-01 | スリーエム イノベイティブ プロパティズ カンパニー | 透明粘着シート |
| WO2014044562A1 (en) * | 2012-09-18 | 2014-03-27 | Basf Se | Polymers comprising a polyurethane backbone endcapped with reactive (meth)acrylic terminating groups and their use as adhesives |
| US9181460B2 (en) * | 2013-03-06 | 2015-11-10 | H.B. Fuller Company | Gas transmitting polyurethane adhesive |
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| CN103436213B (zh) * | 2013-09-09 | 2014-11-19 | 烟台德邦科技有限公司 | 一种紫外线固化型光学树脂黏合剂及其制备方法 |
| DE102014204465A1 (de) * | 2014-03-11 | 2015-09-17 | Henkel Ag & Co. Kgaa | UV-reaktiver Schmelzklebstoff für die Laminierung transparenter Folien |
| JP6491864B2 (ja) * | 2014-12-05 | 2019-03-27 | ヘンケルジャパン株式会社 | 積層シート用接着剤 |
| CN107207677B (zh) * | 2014-12-16 | 2021-07-09 | 亚什兰许可和知识产权有限公司 | 包含键接有乙烯基的丙烯酸系聚合物的电子束可固化的压敏粘合剂 |
| EP3184568A1 (en) * | 2015-12-21 | 2017-06-28 | Evonik Degussa GmbH | Acrylate-terminated urethane polybutadienes from low-monomer 1:1 monoadductes from reactive olefinic compounds and diisocyanates and hydroxy-terminated polybutadienes for liquid optically clear adhesives (locas) |
| EP3184567A1 (de) * | 2015-12-21 | 2017-06-28 | Evonik Degussa GmbH | Acrylatterminierte urethanpolybutadiene aus monomerarmen 1:1 monoaddukten aus reaktiven olfinischen verbindungen und diisocyanaten und hydroxyterminierten polybutadienen |
| BR112019020418B1 (pt) * | 2017-03-30 | 2023-02-28 | Dow Global Technologies Llc | Composição adesiva de fusão a quente de poliuretano e laminado |
| JP6919529B2 (ja) | 2017-11-28 | 2021-08-18 | 株式会社デンソー | 硬化性樹脂組成物およびこれを用いた電装部品 |
| FR3078339B1 (fr) * | 2018-02-23 | 2020-01-24 | Bostik Sa | Composition a base de polyurethane comprenant au moins deux fonctions acrylique |
| EP3999569A1 (en) | 2019-07-17 | 2022-05-25 | Arkema France | (meth)acrylate-functionalized oligomers and methods of preparing and using such oligomers |
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| CN115449326B (zh) * | 2022-10-11 | 2023-05-19 | 东莞市德聚胶接技术有限公司 | 一种抗冲击uv固化围堰胶及其制备方法 |
| CN116179071B (zh) * | 2022-11-17 | 2024-03-08 | 武汉瑞普赛技术有限公司 | 一种柔性印刷版用pet基膜底涂剂及其制备方法和使用方法 |
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| JPH02618A (ja) * | 1987-12-16 | 1990-01-05 | Toyobo Co Ltd | 放射線硬化型樹脂及びそれを用いた磁気記録媒体 |
| JP2007186598A (ja) * | 2006-01-13 | 2007-07-26 | Toyo Seikan Kaisha Ltd | 耐アルカリ性ガラスコーティング用有機−無機ハイブリッド体 |
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| JPS5986045A (ja) * | 1982-11-05 | 1984-05-18 | Nippon Soda Co Ltd | 永久レジスト用光硬化性樹脂組成物 |
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| DE3705090A1 (de) * | 1987-02-18 | 1988-09-01 | Bayer Ag | Neue lackbindemittel fuer die kunststofflackierung |
| DE19800676A1 (de) * | 1998-01-10 | 1999-07-15 | Henkel Kgaa | Verwendung ausgewählter Klebstoffgemische für die Überlappungsverklebung von Rundumetiketten bei ihrem Auftrag auf Kunststoff-Flaschen |
| DE19858694A1 (de) * | 1998-12-18 | 2000-06-21 | Henkel Kgaa | Verwendung reaktiv aushärtender Kleberkomponenten in Schmelzklebern für die Kartonagenverpackung |
| DE19961342B4 (de) * | 1999-12-17 | 2004-02-19 | 3M Espe Ag | Radikalisch härtbare Urethanpräpolymere und deren Verwendung |
| US20020099110A1 (en) * | 1999-12-30 | 2002-07-25 | Tyson Norlin | Radiation-curable coating composition |
| DE10010994A1 (de) * | 2000-03-07 | 2001-09-20 | Goldschmidt Ag Th | Verfahren zur Herstellung von strahlenhärtbaren Bindemitteln und die damit hergestellten Beschichtungen |
| JP4868654B2 (ja) * | 2001-04-13 | 2012-02-01 | 日本合成化学工業株式会社 | 活性エネルギー線硬化型粘着剤組成物、および該組成物の製造方法 |
| US7358295B2 (en) * | 2002-04-05 | 2008-04-15 | Lubrizol Advanced Materials, Inc. | Hybrid polymer composition, and article therefrom |
| US7189781B2 (en) * | 2003-03-13 | 2007-03-13 | H.B. Fuller Licensing & Finance Inc. | Moisture curable, radiation curable sealant composition |
| US7368171B2 (en) * | 2004-09-03 | 2008-05-06 | H.B. Fuller Licensing & Financing, Inc. | Laminating adhesive, laminate including the same, and method of making a laminate |
-
2005
- 2005-01-06 US US10/584,299 patent/US20070179254A1/en not_active Abandoned
- 2005-01-06 KR KR1020067016220A patent/KR20060122919A/ko not_active Ceased
- 2005-01-06 WO PCT/EP2005/050046 patent/WO2005068529A1/en not_active Ceased
- 2005-01-06 CN CN2005800024804A patent/CN1910215B/zh not_active Expired - Fee Related
- 2005-01-06 JP JP2006548304A patent/JP2007523227A/ja active Pending
- 2005-01-06 EP EP20050707746 patent/EP1706440A1/en not_active Withdrawn
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JPH02618A (ja) * | 1987-12-16 | 1990-01-05 | Toyobo Co Ltd | 放射線硬化型樹脂及びそれを用いた磁気記録媒体 |
| JP2007186598A (ja) * | 2006-01-13 | 2007-07-26 | Toyo Seikan Kaisha Ltd | 耐アルカリ性ガラスコーティング用有機−無機ハイブリッド体 |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011508057A (ja) * | 2007-12-27 | 2011-03-10 | スリーエム イノベイティブ プロパティズ カンパニー | 尿素系感圧性接着剤 |
| JP2012526894A (ja) * | 2009-05-15 | 2012-11-01 | スリーエム イノベイティブ プロパティズ カンパニー | ウレタン系感圧接着剤 |
| JP2015232133A (ja) * | 2009-05-15 | 2015-12-24 | スリーエム イノベイティブ プロパティズ カンパニー | ウレタン系感圧接着剤 |
| JP2011162770A (ja) * | 2010-01-15 | 2011-08-25 | Toyo Ink Sc Holdings Co Ltd | 活性エネルギー線硬化型接着剤 |
| JP2013532244A (ja) * | 2010-06-29 | 2013-08-15 | スリーエム イノベイティブ プロパティズ カンパニー | 窓フィルムの適用方法 |
| JP2013539493A (ja) * | 2010-08-26 | 2013-10-24 | スリーエム イノベイティブ プロパティズ カンパニー | 多層状両面接着剤 |
| WO2012165201A1 (ja) * | 2011-06-02 | 2012-12-06 | 株式会社きもと | 易剥離性粘着フィルム |
| JPWO2012165201A1 (ja) * | 2011-06-02 | 2015-02-23 | 株式会社きもと | 易剥離性粘着フィルム |
| JP2013166877A (ja) * | 2012-02-16 | 2013-08-29 | Nitto Denko Corp | 放射線硬化型粘着剤組成物の製造方法、該製造方法で得られた放射線硬化型粘着剤組成物、および、該粘着剤組成物を用いた粘着シート |
| JP2015003519A (ja) * | 2013-01-23 | 2015-01-08 | デクセリアルズ株式会社 | 親水性積層体、及びその製造方法、防汚用積層体、物品、及びその製造方法、並びに防汚方法 |
| JP2014210902A (ja) * | 2013-04-22 | 2014-11-13 | Dic株式会社 | 紫外線硬化型粘着剤組成物及び粘着剤 |
| JP2017521505A (ja) * | 2014-05-08 | 2017-08-03 | アルケマ フランス | 硬化性ウレタン(メタ)アクリレートポリマー組成物および方法 |
| WO2023017835A1 (ja) * | 2021-08-10 | 2023-02-16 | 旭化成株式会社 | ポリイソシアネート組成物、硬化膜、粘着性樹脂組成物、粘着性樹脂シート、及び積層フィルム |
| JPWO2023017835A1 (https=) * | 2021-08-10 | 2023-02-16 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1910215A (zh) | 2007-02-07 |
| EP1706440A1 (en) | 2006-10-04 |
| WO2005068529A1 (en) | 2005-07-28 |
| CN1910215B (zh) | 2011-07-06 |
| KR20060122919A (ko) | 2006-11-30 |
| US20070179254A1 (en) | 2007-08-02 |
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