CA2853022C - Curable liquids and inkjet inks for food packaging applications - Google Patents
Curable liquids and inkjet inks for food packaging applications Download PDFInfo
- Publication number
- CA2853022C CA2853022C CA2853022A CA2853022A CA2853022C CA 2853022 C CA2853022 C CA 2853022C CA 2853022 A CA2853022 A CA 2853022A CA 2853022 A CA2853022 A CA 2853022A CA 2853022 C CA2853022 C CA 2853022C
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- Canada
- Prior art keywords
- polymerizable
- polymeric
- group
- radiation curable
- oligomeric
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000007788 liquid Substances 0.000 title claims abstract description 58
- 239000000976 ink Substances 0.000 title description 108
- 235000013305 food Nutrition 0.000 title description 14
- 238000004806 packaging method and process Methods 0.000 title description 13
- 230000005855 radiation Effects 0.000 claims abstract description 112
- 150000001875 compounds Chemical class 0.000 claims abstract description 64
- 239000000178 monomer Substances 0.000 claims abstract description 53
- 239000000758 substrate Substances 0.000 claims abstract description 43
- 239000003054 catalyst Substances 0.000 claims abstract description 25
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 19
- 150000003254 radicals Chemical class 0.000 claims abstract description 15
- 238000013508 migration Methods 0.000 claims abstract description 14
- 230000005012 migration Effects 0.000 claims abstract description 14
- GTPROMYYPGDANE-UHFFFAOYSA-N ethenoxyethene;prop-2-enoic acid Chemical compound C=COC=C.OC(=O)C=C GTPROMYYPGDANE-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000003999 initiator Substances 0.000 claims description 53
- 239000002270 dispersing agent Substances 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 35
- 238000007641 inkjet printing Methods 0.000 claims description 32
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 28
- 238000007639 printing Methods 0.000 claims description 22
- 239000004094 surface-active agent Substances 0.000 claims description 21
- 229920000642 polymer Polymers 0.000 claims description 17
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 16
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 15
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical group C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 11
- 229920000098 polyolefin Polymers 0.000 claims description 9
- 229920001328 Polyvinylidene chloride Polymers 0.000 claims description 8
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 8
- 239000001913 cellulose Substances 0.000 claims description 8
- 229920002678 cellulose Polymers 0.000 claims description 8
- 229920000728 polyester Polymers 0.000 claims description 8
- 239000005033 polyvinylidene chloride Substances 0.000 claims description 8
- 239000004793 Polystyrene Substances 0.000 claims description 7
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 7
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 7
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 7
- 229920002223 polystyrene Polymers 0.000 claims description 7
- 239000004800 polyvinyl chloride Substances 0.000 claims description 7
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 7
- 239000012463 white pigment Substances 0.000 claims description 7
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 6
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 6
- 239000004417 polycarbonate Substances 0.000 claims description 6
- 229920000515 polycarbonate Polymers 0.000 claims description 6
- JFLRBGOBOJWPHI-UHFFFAOYSA-N pyridin-1-ium-1-sulfonate Chemical compound [O-]S(=O)(=O)[N+]1=CC=CC=C1 JFLRBGOBOJWPHI-UHFFFAOYSA-N 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 5
- 229920002647 polyamide Polymers 0.000 claims description 5
- 238000009792 diffusion process Methods 0.000 abstract description 41
- 239000006185 dispersion Substances 0.000 description 49
- -1 Aliphatic amines Chemical class 0.000 description 48
- 239000000049 pigment Substances 0.000 description 48
- 239000002245 particle Substances 0.000 description 22
- 229910052799 carbon Inorganic materials 0.000 description 19
- 239000004698 Polyethylene Substances 0.000 description 15
- 239000010410 layer Substances 0.000 description 15
- 239000000243 solution Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
- 238000003801 milling Methods 0.000 description 12
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 10
- 239000003112 inhibitor Substances 0.000 description 10
- 229920000573 polyethylene Polymers 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 229920001296 polysiloxane Polymers 0.000 description 9
- 239000004743 Polypropylene Substances 0.000 description 8
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 8
- 229920001155 polypropylene Polymers 0.000 description 8
- 239000002966 varnish Substances 0.000 description 8
- 239000003086 colorant Substances 0.000 description 7
- 239000005022 packaging material Substances 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- AUHIKFMUZNXFKJ-UHFFFAOYSA-N 1-fluoro-4-hydroxythioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2F AUHIKFMUZNXFKJ-UHFFFAOYSA-N 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 125000002091 cationic group Chemical group 0.000 description 6
- 125000004185 ester group Chemical group 0.000 description 6
- 239000012632 extractable Substances 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- 239000000523 sample Substances 0.000 description 5
- URQQDYIVGXOEDA-UHFFFAOYSA-N 2-(2-ethenoxyethoxy)ethyl prop-2-enoate Chemical compound C=COCCOCCOC(=O)C=C URQQDYIVGXOEDA-UHFFFAOYSA-N 0.000 description 4
- ZSTGLUKLFCTSOY-UHFFFAOYSA-N 4-(2,3-dihydroxypropoxy)-1-fluorothioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C(OCC(O)CO)=CC=C2F ZSTGLUKLFCTSOY-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000011324 bead Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- AAOVKJBEBIDNHE-UHFFFAOYSA-N diazepam Chemical compound N=1CC(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 AAOVKJBEBIDNHE-UHFFFAOYSA-N 0.000 description 4
- 239000003480 eluent Substances 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 150000003009 phosphonic acids Chemical class 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000006104 solid solution Substances 0.000 description 4
- 229910002076 stabilized zirconia Inorganic materials 0.000 description 4
- 150000003460 sulfonic acids Chemical class 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 229910052727 yttrium Inorganic materials 0.000 description 4
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical group OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 3
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 238000002296 dynamic light scattering Methods 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 125000005439 maleimidyl group Chemical group C1(C=CC(N1*)=O)=O 0.000 description 3
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical group CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 3
- 125000001624 naphthyl group Chemical group 0.000 description 3
- 125000002560 nitrile group Chemical group 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 239000006069 physical mixture Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 3
- 125000000547 substituted alkyl group Chemical group 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- 229920001567 vinyl ester resin Polymers 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- VFFFESPCCPXZOQ-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;oxirane Chemical compound C1CO1.OCC(CO)(CO)CO VFFFESPCCPXZOQ-UHFFFAOYSA-N 0.000 description 2
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 2
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical group C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-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
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
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- 238000002441 X-ray diffraction Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
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- 125000003158 alcohol group Chemical group 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
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- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
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- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 2
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- 235000014113 dietary fatty acids Nutrition 0.000 description 2
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
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- 229910052782 aluminium Inorganic materials 0.000 description 1
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- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
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- 230000003197 catalytic effect Effects 0.000 description 1
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- PBAYDYUZOSNJGU-UHFFFAOYSA-N chelidonic acid Natural products OC(=O)C1=CC(=O)C=C(C(O)=O)O1 PBAYDYUZOSNJGU-UHFFFAOYSA-N 0.000 description 1
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- 229920000736 dendritic polymer Polymers 0.000 description 1
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- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
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- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
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- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 235000021149 fatty food Nutrition 0.000 description 1
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- 238000011049 filling Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000005003 food packaging material Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
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- 238000000691 measurement method Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
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- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 238000007645 offset printing Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000005026 oriented polypropylene Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
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- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
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- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
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- 125000005017 substituted alkenyl group Chemical group 0.000 description 1
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- 150000005846 sugar alcohols Polymers 0.000 description 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
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- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 description 1
- 229940103494 thiosalicylic acid Drugs 0.000 description 1
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- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/0047—Digital printing on surfaces other than ordinary paper by ink-jet printing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5209—Coatings prepared by radiation-curing, e.g. using photopolymerisable compositions
-
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
-
- 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
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/322—Pigment inks
-
- 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
- C09D11/00—Inks
- C09D11/54—Inks based on two liquids, one liquid being the ink, the other liquid being a reaction solution, a fixer or a treatment solution for the ink
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11193943.5 | 2011-12-16 | ||
| EP11193943.5A EP2604663B1 (en) | 2011-12-16 | 2011-12-16 | Curable liquids and inkjet inks for food packaging applications |
| US201161577102P | 2011-12-19 | 2011-12-19 | |
| US61/577,102 | 2011-12-19 | ||
| PCT/EP2012/074099 WO2013087427A1 (en) | 2011-12-16 | 2012-11-30 | Curable liquids and inkjet inks for food packaging applications |
Publications (2)
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|---|---|
| CA2853022A1 CA2853022A1 (en) | 2013-06-20 |
| CA2853022C true CA2853022C (en) | 2016-07-12 |
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|---|---|---|---|
| CA2853022A Expired - Fee Related CA2853022C (en) | 2011-12-16 | 2012-11-30 | Curable liquids and inkjet inks for food packaging applications |
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| Country | Link |
|---|---|
| US (1) | US9718971B2 (enExample) |
| EP (1) | EP2604663B1 (enExample) |
| CN (1) | CN104039898B (enExample) |
| AU (1) | AU2012350964B2 (enExample) |
| BR (1) | BR112014013586A8 (enExample) |
| CA (1) | CA2853022C (enExample) |
| IN (1) | IN2014CN04309A (enExample) |
| WO (1) | WO2013087427A1 (enExample) |
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| US11470814B2 (en) | 2011-12-05 | 2022-10-18 | Radio Systems Corporation | Piezoelectric detection coupling of a bark collar |
| JP5758832B2 (ja) * | 2012-03-30 | 2015-08-05 | 富士フイルム株式会社 | 活性線硬化型インクジェットインク組成物、インクジェット記録方法、及び、印刷物 |
| JP5718845B2 (ja) * | 2012-03-30 | 2015-05-13 | 富士フイルム株式会社 | インクジェット記録方法及び印刷物 |
| PL2848659T3 (pl) * | 2013-09-16 | 2018-02-28 | Agfa Graphics Nv | Kompozycje utwardzalne radiacyjnie do opakowań żywności |
| EP2868721B1 (en) * | 2013-10-29 | 2018-01-17 | Agfa Nv | Radiation curable brown inkjet ink |
| GB201406683D0 (en) | 2014-04-14 | 2014-05-28 | Montanuniversitat Leoben | Resin composition suitable for printing and printing method utilizing the same |
| BR112016024048A2 (pt) * | 2014-04-15 | 2017-08-15 | Agfa Graphics Nv | tintas para impressão a jato de tinta a base de resina aquosa |
| EP3250636B1 (en) | 2015-01-27 | 2020-05-06 | Hewlett-Packard Development Company, L.P. | Polymeric amine synergists |
| EP3250649B1 (en) * | 2015-01-27 | 2020-06-24 | Hewlett-Packard Development Company, L.P. | Polymeric photoactive agents |
| US10414927B2 (en) | 2015-01-27 | 2019-09-17 | Hewlett-Packard Development Company, L.P. | Polymeric photo active agents |
| US10364363B2 (en) | 2015-01-30 | 2019-07-30 | Hewlett-Packard Development Company, L.P. | Radiation curable binder dispersion |
| US10303991B2 (en) | 2015-07-27 | 2019-05-28 | Hewlett-Packard Development Company, L.P. | Modifying an inkjet raster image for a visible independent effect |
| JP6707858B2 (ja) * | 2015-12-25 | 2020-06-10 | 株式会社リコー | 活性エネルギー線硬化型インク、インク収容容器、２次元又は３次元の像形成装置、２次元又は３次元の像形成方法、及びインクジェット積層硬化物 |
| CN114605866B (zh) * | 2016-02-25 | 2024-04-30 | 维罗斯-纯粹数字有限公司 | 印刷制剂和方法 |
| EP3260505B1 (en) * | 2016-06-22 | 2019-11-06 | Agfa Nv | Methods of manufacturing packaging for food, cosmetics and pharma |
| EP3475370B1 (en) * | 2016-06-23 | 2020-08-05 | Agfa Nv | Polymerizable photoinitiators |
| US10821760B2 (en) | 2017-01-31 | 2020-11-03 | Hewlett-Packard Development Company, L.P. | Inkjet printing |
| US10857825B2 (en) | 2017-01-31 | 2020-12-08 | Hewlett-Packard Development Company, L.P. | Inkjet printing |
| US10723901B2 (en) | 2017-01-31 | 2020-07-28 | Hewlett-Packard Development Company, L.P. | Inkjet ink composition |
| US10723897B2 (en) | 2017-01-31 | 2020-07-28 | Hewlett-Packard Development Company, L.P. | Inkjet compositions |
| WO2018143964A1 (en) | 2017-01-31 | 2018-08-09 | Hewlett-Packard Development Company, L.P. | Inkjet printing |
| EP3388815A1 (en) * | 2017-04-11 | 2018-10-17 | hubergroup Deutschland GmbH | Method for determining the migration potential of an at least partially cured energy curing ink and/or varnish printed on a substrate and especially of a printed food packing |
| CA3062444A1 (en) * | 2017-05-19 | 2018-11-22 | Etna-Tec, Ltd | Methods for making functionalized fluorinated monomers, fluorinated monomers, and compositions for making the same |
| WO2019032425A1 (en) | 2017-08-10 | 2019-02-14 | Sun Chemical Corporation | UV-CURABLE COMPOSITIONS COMPRISING ACYLPHOSPHINE OXIDE PHOTO-INITIATORS |
| WO2019059948A1 (en) | 2017-09-25 | 2019-03-28 | Hewlett-Packard Development Company, L.P. | METHOD AND APPARATUS FOR INK JET PRINTING |
| WO2019059947A1 (en) * | 2017-09-25 | 2019-03-28 | Hewlett-Packard Development Company, L.P. | METHOD AND APPARATUS FOR INK JET PRINTING |
| CN111512452B (zh) * | 2017-10-17 | 2023-11-21 | 科迪华公司 | 用于显示装置的具有高量子点浓度的油墨组合物 |
| GB2575793A (en) | 2018-07-20 | 2020-01-29 | Montanuniv Leoben | Resin composition suitable for printing and printing methods |
| JP6649549B1 (ja) | 2018-11-28 | 2020-02-19 | 東洋インキＳｃホールディングス株式会社 | 活性エネルギー線硬化型インクジェットインキ、インクジェット記録物、及び、インクジェット記録物の製造方法 |
| EP3686251B1 (en) * | 2019-01-24 | 2021-11-17 | Agfa Nv | Radiation curable inkjet inks for interior decoration |
| US12152155B2 (en) * | 2019-07-11 | 2024-11-26 | Sun Chemical Corporation | Direct food contact inks |
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|---|---|---|---|---|
| DE3534645A1 (de) | 1985-09-28 | 1987-04-02 | Merck Patent Gmbh | Copolymerisierbare fotoinitiatoren |
| DE3844444A1 (de) | 1988-12-31 | 1990-08-09 | Basf Ag | Strahlungsempfindliche, ethylenisch ungesaettigte, copolymerisierbare verbindungen und verfahren zu deren herstellung |
| US5248805A (en) * | 1988-12-31 | 1993-09-28 | Basf Aktiengesellschaft | Radiation-senstive, ethylenically unsaturated, copolymerizable compounds and their preparation |
| EP1561791B1 (en) | 1998-10-29 | 2016-03-16 | Agfa Graphics N.V. | New ink compositions for ink jet printing |
| US6803112B1 (en) | 2000-03-29 | 2004-10-12 | Sun Chemical Corporation | Radiation curable aqueous compositions for low extractable film packaging |
| US6500981B1 (en) * | 2000-08-02 | 2002-12-31 | Ethox Chemicals Llc | Hydroxy and sulfonic acid substituted alkenes and salts |
| GB0125099D0 (en) | 2001-10-18 | 2001-12-12 | Coates Brothers Plc | Multi-functional photoinitiators |
| GB0125098D0 (en) * | 2001-10-18 | 2001-12-12 | Coates Brothers Plc | Multi-functional thioxanthone photoinitiators |
| US6767980B2 (en) | 2002-04-19 | 2004-07-27 | Nippon Shokubai Co., Ltd. | Reactive diluent and curable resin composition |
| BRPI0410118B1 (pt) | 2003-05-06 | 2013-12-24 | Ciba Sc Holding Ag | Fotoiniciador trifuncional, seu processo de preparação, sua composição, seu uso, e processo para produção de uma superfície durável resistente a arranhão |
| ITVA20030040A1 (it) | 2003-10-27 | 2005-04-28 | Lamberti Spa | Fotoiniziatore solido bianco in polvere e procedimento per la sua preparazione. |
| EP2664629B1 (en) * | 2004-02-02 | 2014-11-12 | Basf Se | Functionalised photoinitiators |
| EP1616922B1 (en) | 2004-07-15 | 2007-08-29 | Agfa Graphics N.V. | Novel radiation curable compositions |
| EP1616920B1 (en) | 2004-07-15 | 2008-02-20 | Agfa Graphics N.V. | Novel polymeric initiators |
| EP1616897B1 (en) | 2004-07-15 | 2010-03-31 | Agfa Graphics N.V. | Novel polymeric co-initiators |
| EP1616921B1 (en) | 2004-07-15 | 2007-10-31 | Agfa Graphics N.V. | Novel radiation curable compositions |
| EP1616899B2 (en) | 2004-07-15 | 2014-07-02 | Agfa Graphics N.V. | Novel photoreactive polymers |
| US7507773B2 (en) | 2004-07-15 | 2009-03-24 | Agfa Graphics N.V. | Radiation curable compositions |
| US7396861B2 (en) | 2004-07-15 | 2008-07-08 | Agfa Graphics Nv | Radiation curable compositions |
| WO2007018425A1 (en) * | 2005-08-05 | 2007-02-15 | Fujifilm Manufacturing Europe B.V. | Porous membrane and recording medium comprising same |
| JP4799987B2 (ja) * | 2005-09-30 | 2011-10-26 | 富士フイルム株式会社 | インクジェット用インク組成物 |
| PL1790696T3 (pl) | 2005-11-28 | 2013-09-30 | Agfa Nv | Niewodne dyspersje pigmentowe zawierające specyficzne synergetyki dyspersji |
| ES2322276T3 (es) | 2005-11-28 | 2009-06-18 | Agfa Graphics N.V. | Dispersiones de quinacridona no acuosas para utilizacion en sinergicos de dispersion. |
| ES2376465T3 (es) | 2005-11-28 | 2012-03-14 | Agfa Graphics N.V. | Dispersiones de pigmentos no acuosas que contienen sinergistas de dispersión espec�?ficos. |
| ATE464356T1 (de) | 2005-11-28 | 2010-04-15 | Agfa Graphics Nv | Nichtwässrige diketopyrrolo-pyrrol pigmentdispersionen unter verwendung von dispersionssynergisten |
| EP1911814B2 (en) | 2006-10-11 | 2023-07-12 | Agfa Nv | Methods for preparing curable pigment inkjet ink sets |
| ES2342189T3 (es) | 2006-12-21 | 2010-07-02 | Agfa Graphics N.V. | Metodo de impresion por chorro de tinta y cartuchos de tinta. |
| JP5224699B2 (ja) * | 2007-03-01 | 2013-07-03 | 富士フイルム株式会社 | インク組成物、インクジェット記録方法、印刷物、平版印刷版の製造方法、及び平版印刷版 |
| ATE537231T1 (de) * | 2007-10-24 | 2011-12-15 | Agfa Graphics Nv | Strahlenhärtbare tintenstrahldruckfarben und tinten mit verbesserter vergilbungsbeständigkeit |
| DE602007009698D1 (de) | 2007-10-24 | 2010-11-18 | Agfa Gevaert Nv | Härtbare Flüssigkeiten und Tinten für Spielzeuge und Lebensmittelverpackungen |
| PL2325270T3 (pl) | 2007-10-24 | 2013-02-28 | Agfa Nv | Utwardzalne ciecze i tusze do zastosowań w zabawkach i w opakowaniach żywności |
| PL2053099T3 (pl) | 2007-10-24 | 2011-05-31 | Agfa Nv | Biały tusz do drukarki strumieniowej ulepszony pod względem trwałości dyspersji |
| KR101215459B1 (ko) * | 2008-03-27 | 2012-12-26 | 도쿄 프린팅 잉크 엠에프지. 캄파니 리미티드 | 에칭 레지스트용 잉크젯 잉크 조성물 |
| US8034538B2 (en) * | 2009-02-13 | 2011-10-11 | Eastman Kodak Company | Negative-working imageable elements |
| US8883873B2 (en) * | 2009-05-18 | 2014-11-11 | Agfa Graphics Nv | Polymerizable polymeric photoinitiators and radiation curable compositions |
-
2011
- 2011-12-16 EP EP11193943.5A patent/EP2604663B1/en active Active
-
2012
- 2012-11-30 WO PCT/EP2012/074099 patent/WO2013087427A1/en not_active Ceased
- 2012-11-30 IN IN4309CHN2014 patent/IN2014CN04309A/en unknown
- 2012-11-30 US US14/351,596 patent/US9718971B2/en active Active
- 2012-11-30 BR BR112014013586A patent/BR112014013586A8/pt active Search and Examination
- 2012-11-30 CN CN201280062153.8A patent/CN104039898B/zh active Active
- 2012-11-30 CA CA2853022A patent/CA2853022C/en not_active Expired - Fee Related
- 2012-11-30 AU AU2012350964A patent/AU2012350964B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| US20140285568A1 (en) | 2014-09-25 |
| CN104039898A (zh) | 2014-09-10 |
| AU2012350964A1 (en) | 2014-04-17 |
| EP2604663B1 (en) | 2017-08-09 |
| WO2013087427A1 (en) | 2013-06-20 |
| CN104039898B (zh) | 2016-07-06 |
| CA2853022A1 (en) | 2013-06-20 |
| BR112014013586A2 (pt) | 2017-06-13 |
| BR112014013586A8 (pt) | 2017-06-13 |
| IN2014CN04309A (enExample) | 2015-09-04 |
| AU2012350964B2 (en) | 2016-04-14 |
| US9718971B2 (en) | 2017-08-01 |
| EP2604663A1 (en) | 2013-06-19 |
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| EEER | Examination request |
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| MKLA | Lapsed |
Effective date: 20211130 |