DE102009001775A1 - (Meth)acrylatpolymere und deren Verwendung als polymergebundene UV-Initiatoren oder Zusatz zu UV-härtbaren Harzen - Google Patents
(Meth)acrylatpolymere und deren Verwendung als polymergebundene UV-Initiatoren oder Zusatz zu UV-härtbaren Harzen Download PDFInfo
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- DE102009001775A1 DE102009001775A1 DE102009001775A DE102009001775A DE102009001775A1 DE 102009001775 A1 DE102009001775 A1 DE 102009001775A1 DE 102009001775 A DE102009001775 A DE 102009001775A DE 102009001775 A DE102009001775 A DE 102009001775A DE 102009001775 A1 DE102009001775 A1 DE 102009001775A1
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- Prior art keywords
- meth
- polymer
- acrylate
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- polymer according
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- 229920000642 polymer Polymers 0.000 title claims abstract description 72
- 229920005989 resin Polymers 0.000 title claims abstract description 19
- 239000011347 resin Substances 0.000 title claims abstract description 19
- 229920000058 polyacrylate Polymers 0.000 title claims abstract description 13
- 239000003999 initiator Substances 0.000 title claims description 16
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 47
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 35
- 239000000203 mixture Substances 0.000 claims abstract description 34
- 239000000178 monomer Substances 0.000 claims abstract description 33
- 238000007639 printing Methods 0.000 claims abstract description 18
- 239000000654 additive Substances 0.000 claims abstract description 10
- 239000003085 diluting agent Substances 0.000 claims abstract description 9
- 230000000996 additive effect Effects 0.000 claims abstract description 8
- 238000010557 suspension polymerization reaction Methods 0.000 claims abstract description 7
- 239000000470 constituent Substances 0.000 claims abstract description 5
- 239000000725 suspension Substances 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 26
- 239000001257 hydrogen Substances 0.000 claims description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims description 26
- 229910052760 oxygen Inorganic materials 0.000 claims description 24
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 23
- 239000001301 oxygen Substances 0.000 claims description 21
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 20
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- 125000003118 aryl group Chemical group 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 13
- RUDUCNPHDIMQCY-UHFFFAOYSA-N [3-(2-sulfanylacetyl)oxy-2,2-bis[(2-sulfanylacetyl)oxymethyl]propyl] 2-sulfanylacetate Chemical compound SCC(=O)OCC(COC(=O)CS)(COC(=O)CS)COC(=O)CS RUDUCNPHDIMQCY-UHFFFAOYSA-N 0.000 claims description 13
- 229910052717 sulfur Inorganic materials 0.000 claims description 13
- 229910052736 halogen Inorganic materials 0.000 claims description 12
- 150000002367 halogens Chemical class 0.000 claims description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 11
- 150000001412 amines Chemical class 0.000 claims description 9
- 150000002431 hydrogen Chemical class 0.000 claims description 9
- 239000011593 sulfur Substances 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- ZDQNWDNMNKSMHI-UHFFFAOYSA-N 1-[2-(2-prop-2-enoyloxypropoxy)propoxy]propan-2-yl prop-2-enoate Chemical compound C=CC(=O)OC(C)COC(C)COCC(C)OC(=O)C=C ZDQNWDNMNKSMHI-UHFFFAOYSA-N 0.000 claims description 4
- OWHSTLLOZWTNTQ-UHFFFAOYSA-N 2-ethylhexyl 2-sulfanylacetate Chemical group CCCCC(CC)COC(=O)CS OWHSTLLOZWTNTQ-UHFFFAOYSA-N 0.000 claims description 4
- 239000011230 binding agent Substances 0.000 claims description 4
- 239000003086 colorant Substances 0.000 claims description 4
- 238000005227 gel permeation chromatography Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000004971 Cross linker Substances 0.000 claims description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 3
- 239000004926 polymethyl methacrylate Substances 0.000 claims description 3
- 125000004185 ester group Chemical group 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 239000000976 ink Substances 0.000 abstract description 17
- -1 heterocyclyl radical Chemical class 0.000 description 58
- 238000000034 method Methods 0.000 description 18
- 150000001875 compounds Chemical class 0.000 description 15
- 150000003254 radicals Chemical group 0.000 description 15
- 239000012965 benzophenone Substances 0.000 description 14
- 239000000243 solution Substances 0.000 description 12
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 11
- 239000000049 pigment Substances 0.000 description 11
- 125000000217 alkyl group Chemical group 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000003505 polymerization initiator Substances 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- 150000008366 benzophenones Chemical class 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000001993 wax Substances 0.000 description 8
- 238000001035 drying Methods 0.000 description 7
- 125000000623 heterocyclic group Chemical group 0.000 description 7
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 7
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 230000009477 glass transition Effects 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- 239000012986 chain transfer agent Substances 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 125000005843 halogen group Chemical group 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- PVXVWWANJIWJOO-UHFFFAOYSA-N 1-(1,3-benzodioxol-5-yl)-N-ethylpropan-2-amine Chemical compound CCNC(C)CC1=CC=C2OCOC2=C1 PVXVWWANJIWJOO-UHFFFAOYSA-N 0.000 description 4
- 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 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
- QMMZSJPSPRTHGB-UHFFFAOYSA-N MDEA Natural products CC(C)CCCCC=CCC=CC(O)=O QMMZSJPSPRTHGB-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 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 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 150000005840 aryl radicals Chemical class 0.000 description 4
- 239000011324 bead Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000002349 favourable effect Effects 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 239000000025 natural resin Substances 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 238000010526 radical polymerization reaction Methods 0.000 description 4
- 238000001542 size-exclusion chromatography Methods 0.000 description 4
- 150000003440 styrenes Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 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 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- 239000000080 wetting agent Chemical class 0.000 description 4
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 3
- 125000004104 aryloxy group Chemical group 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 125000005844 heterocyclyloxy group Chemical group 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000944 linseed oil Substances 0.000 description 3
- 235000021388 linseed oil Nutrition 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 229920005644 polyethylene terephthalate glycol copolymer Polymers 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- DSTUKHPLWATFCG-UHFFFAOYSA-N (2-benzoylphenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1C(=O)C1=CC=CC=C1 DSTUKHPLWATFCG-UHFFFAOYSA-N 0.000 description 2
- YAQQECDXVGSVHR-UHFFFAOYSA-N (4-hydroxyphenyl)-phenylmethanone;2-methylprop-2-enoic acid Chemical compound CC(=C)C(O)=O.C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 YAQQECDXVGSVHR-UHFFFAOYSA-N 0.000 description 2
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 2
- 125000006649 (C2-C20) alkynyl group Chemical group 0.000 description 2
- 125000006625 (C3-C8) cycloalkyloxy group Chemical group 0.000 description 2
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- FLBAYUMRQUHISI-UHFFFAOYSA-N 1,8-naphthyridine Chemical compound N1=CC=CC2=CC=CN=C21 FLBAYUMRQUHISI-UHFFFAOYSA-N 0.000 description 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- XVTPGZQPUZSUKS-UHFFFAOYSA-N 2-(2-oxopyrrolidin-1-yl)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCN1CCCC1=O XVTPGZQPUZSUKS-UHFFFAOYSA-N 0.000 description 2
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 2
- DJKKWVGWYCKUFC-UHFFFAOYSA-N 2-butoxyethyl 2-methylprop-2-enoate Chemical compound CCCCOCCOC(=O)C(C)=C DJKKWVGWYCKUFC-UHFFFAOYSA-N 0.000 description 2
- PGMMQIGGQSIEGH-UHFFFAOYSA-N 2-ethenyl-1,3-oxazole Chemical class C=CC1=NC=CO1 PGMMQIGGQSIEGH-UHFFFAOYSA-N 0.000 description 2
- JDCUKFVNOWJNBU-UHFFFAOYSA-N 2-ethenyl-1,3-thiazole Chemical class C=CC1=NC=CS1 JDCUKFVNOWJNBU-UHFFFAOYSA-N 0.000 description 2
- KQWDURCUENVKII-UHFFFAOYSA-N 2-ethoxyethoxymethyl 2-methylprop-2-enoate Chemical compound CCOCCOCOC(=O)C(C)=C KQWDURCUENVKII-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
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Classifications
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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
- 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
-
- 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
-
- 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
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/18—Suspension polymerisation
-
- 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
- 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
- C08F20/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F20/30—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety
-
- 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
- C08F220/00—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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
-
- 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
- C08F220/00—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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
-
- 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
- C08F220/00—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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/30—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety
-
- 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
- C08F220/00—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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/30—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety
- C08F220/302—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety and two or more oxygen atoms in the alcohol moiety
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions 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; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—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
- C09D133/10—Homopolymers or copolymers of methacrylic acid esters
-
- 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
- C08F220/00—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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009001775A DE102009001775A1 (de) | 2009-03-24 | 2009-03-24 | (Meth)acrylatpolymere und deren Verwendung als polymergebundene UV-Initiatoren oder Zusatz zu UV-härtbaren Harzen |
| CN201080012598.6A CN102361893B (zh) | 2009-03-24 | 2010-02-25 | (甲基)丙烯酸酯聚合物和其作为聚合物键接的uv引发剂或可uv固化树脂的添加剂的用途 |
| KR1020117022237A KR20110139234A (ko) | 2009-03-24 | 2010-02-25 | (메트)아크릴레이트 중합체 및 uv-경화성 수지에 대한 중합체-결합된 uv 개시제 또는 첨가제로서의 그의 용도 |
| JP2012501217A JP5901515B2 (ja) | 2009-03-24 | 2010-02-25 | (メタ)アクリレートポリマー並びに前記ポリマーを、ポリマーに結合された紫外線開始剤として又は紫外線硬化性樹脂への添加剤として用いる使用 |
| EP10705371.2A EP2411426B1 (de) | 2009-03-24 | 2010-02-25 | (meth)acrylatpolymere und deren verwendung als polymergebundene uv-initiatoren oder zusatz zu uv-härtbaren harzen |
| US13/203,993 US20120010317A1 (en) | 2009-03-24 | 2010-02-25 | (meth)acrylate polymers and the use thereof as polymer-bound uv initiators or additive to uv-curable resins |
| HK12105574.9A HK1164905B (en) | 2009-03-24 | 2010-02-25 | (meth)acrylate polymers and the use thereof as polymer-bound uv initiators or additive to uv-curable resins |
| PCT/EP2010/052384 WO2010108752A1 (de) | 2009-03-24 | 2010-02-25 | (meth)acrylatpolymere und deren verwendung als polymergebundene uv-initiatoren oder zusatz zu uv-härtbaren harzen |
| RU2011142635/04A RU2553661C2 (ru) | 2009-03-24 | 2010-02-25 | (мет) акрилатные полимеры и применение их в качестве связанных с полимерами уф-инициаторов или в качестве добавки к отверждаемым уф-светом смолам |
| TW099108188A TWI478947B (zh) | 2009-03-24 | 2010-03-19 | (甲基)丙烯酸酯聚合物及其作為與聚合物結合的uv引發劑或uv可固化樹脂的添加劑之用途 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009001775A DE102009001775A1 (de) | 2009-03-24 | 2009-03-24 | (Meth)acrylatpolymere und deren Verwendung als polymergebundene UV-Initiatoren oder Zusatz zu UV-härtbaren Harzen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102009001775A1 true DE102009001775A1 (de) | 2010-09-30 |
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Family Applications (1)
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| DE102009001775A Withdrawn DE102009001775A1 (de) | 2009-03-24 | 2009-03-24 | (Meth)acrylatpolymere und deren Verwendung als polymergebundene UV-Initiatoren oder Zusatz zu UV-härtbaren Harzen |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20120010317A1 (https=) |
| EP (1) | EP2411426B1 (https=) |
| JP (1) | JP5901515B2 (https=) |
| KR (1) | KR20110139234A (https=) |
| CN (1) | CN102361893B (https=) |
| DE (1) | DE102009001775A1 (https=) |
| RU (1) | RU2553661C2 (https=) |
| TW (1) | TWI478947B (https=) |
| WO (1) | WO2010108752A1 (https=) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2585496A2 (en) * | 2010-06-22 | 2013-05-01 | Coloplast A/S | Hydrophilic gels derived from grafted photoinitiators |
| WO2012145857A1 (en) * | 2011-04-25 | 2012-11-01 | Evonik Röhm Gmbh | Aqueous dispersion of preferably benzophenone-containing (meth)acrylate polymers for leather coating |
| WO2013052105A2 (en) | 2011-10-03 | 2013-04-11 | Biomimedica, Inc. | Polymeric adhesive for anchoring compliant materials to another surface |
| CN103087234A (zh) * | 2011-11-08 | 2013-05-08 | 广州市博兴化工科技有限公司 | 具有光引发活性端基的丙烯酸酯官能性聚合物及其制备方法 |
| BE1020472A5 (nl) * | 2012-03-16 | 2013-11-05 | Arets Graphics | Verbeterde deklagen en werkwijze om deklagen te maken. |
| EP2850111B1 (en) * | 2012-05-16 | 2018-11-21 | Coloplast A/S | Novel polymeric photoinitiators and photoinitiator monomers |
| US9034938B2 (en) * | 2012-09-12 | 2015-05-19 | Basf Se | Photoreactive polymer |
| DE102012216170A1 (de) * | 2012-09-12 | 2014-03-13 | Basf Se | Photoreaktives Polymer |
| TWI585144B (zh) * | 2014-10-21 | 2017-06-01 | Mitsubishi Rayon Co | (Meth) acrylic resin composition and a resin molded product |
| KR101921013B1 (ko) | 2015-01-05 | 2018-11-21 | 아이지엠 몰타 리미티드 | Led-경화성 저 이동 광개시제 |
| JP6791615B2 (ja) * | 2015-03-06 | 2020-11-25 | スリーエム イノベイティブ プロパティズ カンパニー | 紫外線架橋性組成物 |
| BR112017019963A2 (pt) * | 2015-03-20 | 2018-06-19 | Henkel IP & Holding GmbH | fotoiniciadores que são poliméricos ou polimerizáveis para uso em adesivos sensíveis à pressão curáveis por uv |
| RU2741435C2 (ru) * | 2016-08-12 | 2021-01-26 | Дау Глоубл Текнолоджиз Ллк | Чувствительные к давлению адгезивные композиции на водной основе и способы их получения |
| JP7225530B2 (ja) * | 2017-10-30 | 2023-02-21 | 株式会社レゾナック | 無溶剤型樹脂組成物 |
| JP7596656B2 (ja) * | 2020-07-29 | 2024-12-10 | 三菱ケミカル株式会社 | 硬化性組成物、硬化物及び積層体 |
| CN112851845B (zh) * | 2021-01-20 | 2022-04-29 | 东华大学 | 一种共聚高分子光引发剂及其制备方法 |
| CN114855295B (zh) * | 2021-01-20 | 2024-04-05 | 东华大学 | 一种纺丝原液、耐热抗蠕变纤维及其制备方法 |
| CN114854114B (zh) * | 2021-01-20 | 2024-10-18 | 东华大学 | 一种交联聚烯烃及其制备方法 |
| CN113336882B (zh) * | 2021-05-24 | 2022-11-04 | 博立尔化工(扬州)有限公司 | 一种采用间歇式本体聚合法制备窄分子量分布的pmma树脂的工艺 |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3574617A (en) * | 1967-03-30 | 1971-04-13 | Nat Starch Chem Corp | Novel photosensitive coating systems |
| EP0246848A2 (en) * | 1986-05-19 | 1987-11-25 | Minnesota Mining And Manufacturing Company | Pressure-sensitive adhesive crosslinked by copolymerizable aromatic ketone monomers |
| EP0445641A1 (de) * | 1990-03-08 | 1991-09-11 | BASF Aktiengesellschaft | Ethylenisch ungesättigte Verbindungen |
| US5073611A (en) * | 1989-04-29 | 1991-12-17 | Basf Aktiengesellschaft | Copolymers crosslinkable by ultraviolet radiation in the atmosphere |
| EP0346734B1 (de) * | 1988-06-16 | 1993-11-03 | BASF Aktiengesellschaft | Benzophenonderivate und deren Herstellung |
| US5439970A (en) * | 1992-11-04 | 1995-08-08 | Rhone-Poulenc Chimie | Paint latices comprising benzophenone/acrylic copolymerizates |
| US5900472A (en) | 1996-12-23 | 1999-05-04 | Sartomer Technology | Copolymerizable benzophenone photoinitiators |
| EP1316597A2 (de) * | 2001-11-29 | 2003-06-04 | Basf Aktiengesellschaft | Glycidyl(meth)acrylat enthaltende Klebstoff |
| WO2008049932A1 (de) * | 2006-10-27 | 2008-05-02 | Basf Se | Strahlungshärtbare mischung, enthaltend niedermolekulare, ethylenisch ungesättigte verbindungen mit nicht-aromatischen ringsystemen |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4037079A1 (de) * | 1990-11-22 | 1992-05-27 | Basf Ag | Ungesaettigte phenonderivate und ihre verwendung als haftklebstoffe |
| JP3019229B2 (ja) * | 1991-10-24 | 2000-03-13 | 根上工業株式会社 | 記録材料 |
| CA2227192A1 (en) * | 1995-07-19 | 1997-02-06 | Peter Grieshaber | Heterogeneous photo-initiators, photopolymerisable compositions and their use |
| DE19600147A1 (de) * | 1996-01-04 | 1997-07-10 | Basf Lacke & Farben | Verfahren zur Lackierung von Gegenständen unter Verwendung strahlungshärtbarer Pulverlacke |
| JPH10279859A (ja) * | 1997-04-07 | 1998-10-20 | Seiko Epson Corp | 耐光性に優れた画像を実現するインク組成物 |
| DE69936408T2 (de) * | 1998-03-12 | 2007-12-06 | Lucite International Uk Ltd., Southampton | Polymerzusammensetzung |
| US6340719B1 (en) * | 1999-12-29 | 2002-01-22 | 3M-Innovative Properties Company | Crosslinking process |
| JP2002363226A (ja) * | 2001-06-04 | 2002-12-18 | Ipposha Oil Ind Co Ltd | 繊維用高分子紫外線吸収剤及びそれを含む難燃アクリル系繊維 |
| JP2003040937A (ja) * | 2001-07-27 | 2003-02-13 | Ipposha Oil Ind Co Ltd | 高分子光安定剤 |
| RU2338760C2 (ru) * | 2002-12-20 | 2008-11-20 | Циба Спешиалти Кемикэлз Холдинг Инк. | Способ формирования реакционноспособных покрытий |
| JP4265775B2 (ja) * | 2004-02-13 | 2009-05-20 | 一方社油脂工業株式会社 | 光学フィルム用添加剤、それを含む光学フィルム、それを用いた偏光板及び液晶表示装置 |
| DE102004037929A1 (de) * | 2004-08-04 | 2006-03-16 | Rohmax Additives Gmbh | Verfahren zur radikalischen Polymerisation ethylenisch-ungesättigter Verbindungen |
| US7745505B2 (en) * | 2004-12-29 | 2010-06-29 | Henkel Ag & Co. Kgaa | Photoinitiators and UV-crosslinkable acrylic polymers for pressure sensitive adhesives |
| JP4814551B2 (ja) * | 2005-06-07 | 2011-11-16 | 株式会社リコー | 感熱性粘着剤及び粘着材料 |
| JP2007047756A (ja) * | 2005-07-12 | 2007-02-22 | Fujifilm Electronic Materials Co Ltd | 光硬化性組成物、カラーフィルタ及びその製造方法 |
| JP2010209183A (ja) * | 2009-03-09 | 2010-09-24 | Fujifilm Corp | インク組成物及びインクジェット記録方法 |
-
2009
- 2009-03-24 DE DE102009001775A patent/DE102009001775A1/de not_active Withdrawn
-
2010
- 2010-02-25 RU RU2011142635/04A patent/RU2553661C2/ru not_active IP Right Cessation
- 2010-02-25 US US13/203,993 patent/US20120010317A1/en not_active Abandoned
- 2010-02-25 WO PCT/EP2010/052384 patent/WO2010108752A1/de not_active Ceased
- 2010-02-25 EP EP10705371.2A patent/EP2411426B1/de not_active Not-in-force
- 2010-02-25 KR KR1020117022237A patent/KR20110139234A/ko not_active Ceased
- 2010-02-25 CN CN201080012598.6A patent/CN102361893B/zh not_active Expired - Fee Related
- 2010-02-25 JP JP2012501217A patent/JP5901515B2/ja not_active Expired - Fee Related
- 2010-03-19 TW TW099108188A patent/TWI478947B/zh not_active IP Right Cessation
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3574617A (en) * | 1967-03-30 | 1971-04-13 | Nat Starch Chem Corp | Novel photosensitive coating systems |
| EP0246848A2 (en) * | 1986-05-19 | 1987-11-25 | Minnesota Mining And Manufacturing Company | Pressure-sensitive adhesive crosslinked by copolymerizable aromatic ketone monomers |
| EP0346734B1 (de) * | 1988-06-16 | 1993-11-03 | BASF Aktiengesellschaft | Benzophenonderivate und deren Herstellung |
| US5073611A (en) * | 1989-04-29 | 1991-12-17 | Basf Aktiengesellschaft | Copolymers crosslinkable by ultraviolet radiation in the atmosphere |
| EP0445641A1 (de) * | 1990-03-08 | 1991-09-11 | BASF Aktiengesellschaft | Ethylenisch ungesättigte Verbindungen |
| US5439970A (en) * | 1992-11-04 | 1995-08-08 | Rhone-Poulenc Chimie | Paint latices comprising benzophenone/acrylic copolymerizates |
| US5900472A (en) | 1996-12-23 | 1999-05-04 | Sartomer Technology | Copolymerizable benzophenone photoinitiators |
| EP1316597A2 (de) * | 2001-11-29 | 2003-06-04 | Basf Aktiengesellschaft | Glycidyl(meth)acrylat enthaltende Klebstoff |
| WO2008049932A1 (de) * | 2006-10-27 | 2008-05-02 | Basf Se | Strahlungshärtbare mischung, enthaltend niedermolekulare, ethylenisch ungesättigte verbindungen mit nicht-aromatischen ringsystemen |
Non-Patent Citations (13)
| Title |
|---|
| "Macromeolecules, an Introduction to Polymer Science", F. A. Bovey and F. H. Winslow, Editors, Academic Press (1979), 296-312 |
| Carlini et al. berichten in Polymer, 1983, Vol. 24, May, Seite 599 ff. |
| CARLINI,Carlo,et.al.:Polymers containing side-chain benzophenone chromophores:a new class of highly efficient polymerization photoinitiatorts.In:Polymer, 1983, Vol.24, S.599-606 $ganzes Dokument$ * |
| CARLINI,Carlo,et.al.:Polymers containing side-chain benzophenone chromophores:a new class of highly efficient polymerization photoinitiatorts.In:Polymer, 1983, Vol.24, S.599-606 ganzes Dokument |
| DIN EN/SO 6721-2 |
| EN ISO 11357 |
| H. Rausch-Puntigam, T. Völker "Acryl- und Methacrylverbindungen" Springer, Heidelberg, 1967 |
| Houben-Weyl "Methoden der organischen Chemie" Bd. XIV/1, S. 66 ff., Georg Thieme, Heidelberg, 1961 |
| ISO 11357-2 |
| Kirk-Othmer "Encyclopedia of Chemical Technology" Vol. 1, S. 296 ff., J. Wiley, New York, 1978 |
| P. J. Flory, "Principles of Polymer Chemistry" Cornell University Press (1953), Chapter VII, 266-316 |
| Ullmanns' Encyclopedia of Industrial Chemistry, Sixth Edition |
| W. W. Yau, J. J. Kirkland and D. D. Bly, "Modern Size Exclusion Liquid Chromatography, John Wiley and Sons, New York, 1979 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2411426B1 (de) | 2016-08-17 |
| JP5901515B2 (ja) | 2016-04-13 |
| EP2411426A1 (de) | 2012-02-01 |
| JP2012521453A (ja) | 2012-09-13 |
| US20120010317A1 (en) | 2012-01-12 |
| HK1164905A1 (en) | 2012-09-28 |
| WO2010108752A1 (de) | 2010-09-30 |
| RU2553661C2 (ru) | 2015-06-20 |
| CN102361893A (zh) | 2012-02-22 |
| TW201105685A (en) | 2011-02-16 |
| CN102361893B (zh) | 2015-06-17 |
| TWI478947B (zh) | 2015-04-01 |
| KR20110139234A (ko) | 2011-12-28 |
| RU2011142635A (ru) | 2013-04-27 |
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