JP2022525271A - インク組成物 - Google Patents
インク組成物 Download PDFInfo
- Publication number
- JP2022525271A JP2022525271A JP2021541570A JP2021541570A JP2022525271A JP 2022525271 A JP2022525271 A JP 2022525271A JP 2021541570 A JP2021541570 A JP 2021541570A JP 2021541570 A JP2021541570 A JP 2021541570A JP 2022525271 A JP2022525271 A JP 2022525271A
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- JP
- Japan
- Prior art keywords
- ink composition
- pigment
- composition according
- ink
- acrylate
- 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.)
- Granted
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- 239000000203 mixture Substances 0.000 title claims abstract description 201
- 239000003999 initiator Substances 0.000 claims abstract description 51
- 239000000178 monomer Substances 0.000 claims abstract description 48
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 claims abstract description 42
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims abstract description 36
- 239000000049 pigment Substances 0.000 claims description 124
- -1 for example Chemical compound 0.000 claims description 40
- 239000000758 substrate Substances 0.000 claims description 34
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 20
- 238000007639 printing Methods 0.000 claims description 19
- 239000003086 colorant Substances 0.000 claims description 17
- 150000001412 amines Chemical class 0.000 claims description 16
- 239000006229 carbon black Substances 0.000 claims description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 13
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 8
- 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 claims description 8
- 229920000570 polyether Polymers 0.000 claims description 8
- GUCYFKSBFREPBC-UHFFFAOYSA-N [phenyl-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C(=O)C1=C(C)C=C(C)C=C1C GUCYFKSBFREPBC-UHFFFAOYSA-N 0.000 claims description 7
- CZFWMSQKAIGXLS-UHFFFAOYSA-N C=1C=CC=CC=1C(=O)P(=O)C(=O)C1=CC=CC=C1 Chemical group C=1C=CC=CC=1C(=O)P(=O)C(=O)C1=CC=CC=C1 CZFWMSQKAIGXLS-UHFFFAOYSA-N 0.000 claims description 6
- ZMDDERVSCYEKPQ-UHFFFAOYSA-N Ethyl (mesitylcarbonyl)phenylphosphinate Chemical compound C=1C=CC=CC=1P(=O)(OCC)C(=O)C1=C(C)C=C(C)C=C1C ZMDDERVSCYEKPQ-UHFFFAOYSA-N 0.000 claims description 5
- 229920006254 polymer film Polymers 0.000 claims description 4
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 claims description 3
- 229940067265 pigment yellow 138 Drugs 0.000 claims description 3
- WPKYZIPODULRBM-UHFFFAOYSA-N azane;prop-2-enoic acid Chemical compound N.OC(=O)C=C WPKYZIPODULRBM-UHFFFAOYSA-N 0.000 claims description 2
- 238000005576 amination reaction Methods 0.000 claims 1
- 238000000151 deposition Methods 0.000 claims 1
- 238000001723 curing Methods 0.000 abstract description 25
- 238000007641 inkjet printing Methods 0.000 abstract description 11
- 230000001070 adhesive effect Effects 0.000 abstract description 7
- 238000003847 radiation curing Methods 0.000 abstract description 5
- 239000000976 ink Substances 0.000 description 187
- 239000000975 dye Substances 0.000 description 36
- 235000019241 carbon black Nutrition 0.000 description 15
- 239000000123 paper Substances 0.000 description 14
- 239000002270 dispersing agent Substances 0.000 description 12
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 230000001588 bifunctional effect Effects 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- 239000006185 dispersion Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 239000003755 preservative agent Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 239000004909 Moisturizer Substances 0.000 description 8
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 8
- 230000001333 moisturizer Effects 0.000 description 8
- 238000006116 polymerization reaction Methods 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 239000003381 stabilizer Substances 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000000080 wetting agent Substances 0.000 description 7
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
- 241000557626 Corvus corax Species 0.000 description 6
- 241000721047 Danaus plexippus Species 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 238000003848 UV Light-Curing Methods 0.000 description 6
- 230000008878 coupling Effects 0.000 description 6
- 238000010168 coupling process Methods 0.000 description 6
- 238000005859 coupling reaction Methods 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 238000004806 packaging method and process Methods 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 150000003505 terpenes Chemical class 0.000 description 5
- 235000007586 terpenes Nutrition 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 4
- 239000013522 chelant Substances 0.000 description 4
- 239000002482 conductive additive Substances 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 125000004437 phosphorous atom Chemical group 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000002985 plastic film Substances 0.000 description 4
- 229920006255 plastic film Polymers 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 238000010526 radical polymerization reaction Methods 0.000 description 4
- 150000003512 tertiary amines Chemical class 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- YBFHILNBYXCJKD-UHFFFAOYSA-N 1-(6-methylpyridin-3-yl)-2-(4-methylsulfonylphenyl)ethanone Chemical compound C1=NC(C)=CC=C1C(=O)CC1=CC=C(S(C)(=O)=O)C=C1 YBFHILNBYXCJKD-UHFFFAOYSA-N 0.000 description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 3
- LQPXWLZWRGJJNQ-UHFFFAOYSA-N 2-(9-oxothioxanthen-1-yl)oxyacetic acid Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C=CC=C2OCC(=O)O LQPXWLZWRGJJNQ-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 3
- 150000003926 acrylamides Chemical class 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 239000000987 azo dye Substances 0.000 description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 125000004386 diacrylate group Chemical group 0.000 description 3
- 150000005690 diesters Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000012860 organic pigment Substances 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 235000013772 propylene glycol Nutrition 0.000 description 3
- 150000003335 secondary amines Chemical class 0.000 description 3
- 210000003813 thumb Anatomy 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- ARXKVVRQIIOZGF-UHFFFAOYSA-N 1,2,4-butanetriol Chemical compound OCCC(O)CO ARXKVVRQIIOZGF-UHFFFAOYSA-N 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- RXGUIWHIADMCFC-UHFFFAOYSA-N 2-Methylpropyl 2-methylpropionate Chemical compound CC(C)COC(=O)C(C)C RXGUIWHIADMCFC-UHFFFAOYSA-N 0.000 description 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 2
- GTELLNMUWNJXMQ-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical class OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CCC(CO)(CO)CO GTELLNMUWNJXMQ-UHFFFAOYSA-N 0.000 description 2
- LYGZOGDWCOYSGJ-UHFFFAOYSA-N 2-hydroxy-1-[4-[4-(2-hydroxy-2-methylpropanoyl)phenoxy]phenyl]-2-methylpropan-1-one Chemical compound C1=CC(C(=O)C(C)(O)C)=CC=C1OC1=CC=C(C(=O)C(C)(C)O)C=C1 LYGZOGDWCOYSGJ-UHFFFAOYSA-N 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 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 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- 239000004322 Butylated hydroxytoluene Substances 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
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-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
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229930192627 Naphthoquinone Natural products 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 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 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 2
- KNSXNCFKSZZHEA-UHFFFAOYSA-N [3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical class C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C KNSXNCFKSZZHEA-UHFFFAOYSA-N 0.000 description 2
- 239000002318 adhesion promoter Substances 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 239000001000 anthraquinone dye Substances 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N benzoquinolinylidene Natural products C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 125000005626 carbonium group Chemical group 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 2
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
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- 235000019239 indanthrene blue RS Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- MLFHJEHSLIIPHL-UHFFFAOYSA-N isoamyl acetate Chemical compound CC(C)CCOC(C)=O MLFHJEHSLIIPHL-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 2
- 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 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 150000002791 naphthoquinones Chemical class 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- PGMYKACGEOXYJE-UHFFFAOYSA-N pentyl acetate Chemical compound CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 2
- 229940099800 pigment red 48 Drugs 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
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Classifications
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- 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
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
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- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5397—Phosphine oxides
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F220/285—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F226/02—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 a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a single or double bond to nitrogen
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- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
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- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Ink Jet (AREA)
Abstract
Description
本件は2019年1月18日(2019/01/18)出願の英国特許出願第1900725.1号に基づく優先権及び利益を主張し、その内容は全体が参照により本明細書に組み込まれる。
インク組成物はベンジルアクリレートを含有する。ベンジルアクリレートは以下の構造を有する公知の化合物である:
インク組成物はホスフィンオキシド開始剤を含有する。ホスフィンオキシド開始剤は、ビスアシルホスフィンオキシド、例えばジベンゾイルホスフィンオキシド(例えばフェニルビス(2,4,6-トリメチルベンゾイル)ホスフィンオキシド)等、ベンゾイルアルキルホスフィネート、例えばエチル(2,4,6-トリメチルベンゾイル)フェニルホスフィネート等、又はそれらの混合物である。
インク組成物はベンジルアクリレートを含む。ベンジルアクリレートは単官能モノマーである。インク組成物はさらなる単官能モノマーを更に含んでいてもよい。
インク組成物はさらなる開始剤を更に含んでいてもよい。
インク組成物は、多官能モノマー、例えば二官能性又は三官能性モノマーを更に含んでいてもよい。
本発明のインクはアミン化合物を更に含んでいてもよい。
本発明のインクは、有機溶媒、水、又はそれらの混合物等の溶媒を含んでいてもよい。このように、例えばCIJ印刷での使用のために、インクの粘度を更に低下させることができる、又はインクの導電性を高めることができる。
インク組成物及び印刷堆積物は着色剤を含んでいてもよい。着色剤は特に限定されず、当技術分野において公知の任意の適切な着色剤を使用してもよい。
本発明のインク組成物はオリゴマーを更に含んでいてもよい。
インク組成物及び/又は印刷堆積物は、当技術分野において一般的であるもの等のさらなる成分を含有していてもよい(例えば欧州特許公開第2070998号及び欧州特許公開第1788045号を参照)。
好ましくは、インク組成物及び/又は印刷堆積物は安定剤を更に含む。
連続インクジェットの用途において、インク組成物及び/又は印刷堆積物は導電性添加剤を更に含んでいてもよい。導電性添加剤は当技術分野において公知の任意の有機塩であってもよい。
インク組成物及び/又は印刷堆積物は湿潤剤を更に含んでいてもよい。
インク組成物及び/又は印刷堆積物は保湿剤を更に含んでいてもよい。
インク組成物及び/又は印刷堆積物は保存料を更に含んでいてもよい。保存料は、抗酸化剤又は劣化防止剤であってもよい。
インク組成物及び/又は印刷堆積物は界面活性剤を更に含んでいてもよい。
インク組成物及び印刷堆積物は、粘着付与剤を更に含んでいてもよい。
インク組成物及び印刷堆積物は、接着促進剤を更に含んでいてもよい。
インク組成物及び印刷堆積物は、顔料分散剤を更に含んでいてもよい。
インク組成物は、当技術分野において公知の方法を使用して成分を合わせることにより配合される。
本開示は、基材上にマーキングを印刷する方法を提供する。本発明にしたがって任意の適切な基材に印刷してもよい。
本明細書で使用する印刷堆積物という用語は、適切な基材上に印刷され硬化された後のインク組成物を指す。それは、インク組成物中に存在するベンジルアクリレートの少なくとも一部及び任意の他のモノマーを重合させてフィルムが形成される、本発明のインク組成物である。
上記の実施形態のありとあらゆる適合性の高い組み合わせは、ありとあらゆる組み合わせが個々にかつ明確に列挙されるかのごとく、明確に本明細書で開示される。
粘度測定
各試料の粘度を42℃及び25℃で測定して、圧電式ドロップオンデマンド型インクジェットプリンター等のプリンターの典型的な噴射温度及び室温を再現した。
Kバーを有する標準的な展色キットを使用して各試料のフィルムを調製した。フィルムの厚さは使用する基材に依存していた。
インク試料の調製
インク配合物を45gのバッチで製造した。顔料分散物及び界面活性剤を除いて配合物のすべての成分を、不透明な遠心管の中に秤量して入れ、すべての光開始剤の完全な溶解を確実にするように200rpmのスピードで45分振とうした。透明なワニスの存在により溶解を決定し、溶解はすべての9種の試料で観察された。顔料分散物及び界面活性剤を加え200rpmで更に45分振とうした。
インクの試験
実施例1で製造されるインクの各々を、その後上記で概要を述べたように2つの温度で、粘度について試験した。上記で概要を述べたように様々な基材上で表面硬化及び接着性についてもインクを試験した。これらの実験の結果を下記のTable 4(表4)及びTable 5(表5)に示す。
Claims (20)
- ホスフィンオキシド開始剤及びベンジルアクリレートを含むインク組成物であって、
ベンジルアクリレートの量がインク組成物の総質量を基準として40質量%未満であり、且つ単官能モノマーの総量がインク組成物の総質量を基準として45質量%未満であり;
ホスフィンオキシド開始剤が、ビスアシルホスフィンオキシド、ベンゾイルアルキルホスフィネート、又はそれらの混合物である、インク組成物。 - ベンジルアクリレートが、インク組成物の総質量を基準として10~35質量%で存在する、請求項1に記載のインク組成物。
- ホスフィンオキシド開始剤が、ジベンゾイルホスフィンオキシド、ベンゾイルアルキルホスフィネート、又はそれらの混合物である、請求項1又は請求項2に記載のインク組成物。
- ホスフィンオキシド開始剤が、フェニルビス(2,4,6-トリメチルベンゾイル)ホスフィンオキシド及びエチル (2,4,6-トリメチルベンゾイル)フェニルホスフィネートの組み合わせである、請求項3に記載のインク組成物。
- ホスフィンオキシド開始剤がフェニルビス(2,4,6-トリメチルベンゾイル)ホスフィンオキシドである、請求項3に記載のインク組成物。
- ホスフィンオキシド開始剤が、インク組成物の総質量を基準として1~7質量%で存在する、請求項1から5のいずれか一項に記載のインク組成物。
- 多官能モノマーを更に含む、請求項1から6のいずれか一項に記載のインク組成物。
- 多官能性モノマーが、多官能アクリレート、例えばヘキサンジオールジアクリレートである、請求項7に記載のインク組成物。
- 多官能モノマーが、インク組成物の総質量を基準として60~70質量%で存在する、請求項7又は請求項8に記載のインク組成物。
- 着色剤を更に含む、請求項1から9のいずれか一項に記載のインク組成物。
- 着色剤が、顔料、例えばC.I. Pigment Yellow 83、C.I. Pigment Yellow 138、C.I. Pigment Yellow 139、C.I. Pigment Yellow 150、C.I. Pigment Yellow 151、Pigment Yellow 154、C.I. Pigment Yellow 155、C.I. Pigment Yellow 185、C.I. Pigment Orange 43、Pigment Orange 64、C.I. Pigment Orange 73、C.I. Pigment Red 122、C.I. Pigment Red 176、C.I. Pigment Red 254、C.I. Pigment Red 255、C.I. Pigment Red 272、C.I. Pigment Blue 15:3、C.I. Pigment Blue 15:4、C.I. Pigment Green 7、C.I. Pigment Violet 19、C.I. Pigment Violet 23、Pigment Black 7、及びカーボンブラックからなる群から選択されるものである、請求項10に記載のインク組成物。
- 着色剤が、インク組成物の総質量を基準として1~25質量%で存在する、請求項10又は請求項11に記載のインク組成物。
- アミン化合物を更に含む、請求項1から12のいずれか一項に記載のインク組成物。
- アミン化合物が、アミンアクリレート、例えばアミン官能性アクリレートオリゴマーである、請求項13に記載のインク組成物。
- オリゴマーを更に含む、請求項1から14のいずれか一項に記載のインク組成物。
- オリゴマーが、ポリエーテルアクリレート、例えばアミノ化ポリエーテルアクリレートである、請求項15に記載のインク組成物。
- 請求項1から16のいずれか一項に記載のインク組成物を収容したインク容器。
- 請求項1から16のいずれか一項に記載のインク組成物を収容したインク容器を用意する工程と、インク組成物の液滴を吐出する工程と、液滴を基材上に堆積させる工程とを含む、印刷方法。
- 請求項18に記載の方法により生成される、印刷堆積物を含む基材。
- 請求項1から16のいずれか一項に記載のインク組成物を硬化させることにより形成された硬化ポリマーフィルムを含む、印刷堆積物。
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PCT/EP2020/051166 WO2020148441A1 (en) | 2019-01-18 | 2020-01-17 | Ink compositions |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012126885A (ja) * | 2010-11-22 | 2012-07-05 | Seiko Epson Corp | 紫外線硬化型インクジェット用インク組成物 |
JP2012201847A (ja) * | 2011-03-28 | 2012-10-22 | Seiko Epson Corp | 紫外線硬化型インクジェット用インク組成物 |
JP2012255045A (ja) * | 2011-06-07 | 2012-12-27 | Seiko Epson Corp | 光硬化型インクジェット記録用インク組成物、インクジェット記録方法 |
US20150094394A1 (en) * | 2013-10-02 | 2015-04-02 | Samsung Electronics Co., Ltd. | Multi-color ink for 3d printing, 3d printer, and method of controlling the 3d printer |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4896502B2 (ja) | 2005-11-22 | 2012-03-14 | 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、平版印刷版の製造方法、及び平版印刷版 |
JP5419343B2 (ja) | 2007-12-14 | 2014-02-19 | 富士フイルム株式会社 | インクジェット記録用インク組成物、及び、インクジェット記録方法 |
US9056986B2 (en) * | 2010-11-09 | 2015-06-16 | Seiko Epson Corporation | Ultraviolet curable type ink-jet ink composition, recording method and recording apparatus using same |
CN102757693B (zh) * | 2011-04-28 | 2015-11-18 | 精工爱普生株式会社 | 光固化型油墨组合物、记录方法及装置、光固化型喷墨记录用油墨组合物及喷墨记录方法 |
EP3205511B1 (en) * | 2012-03-28 | 2020-12-09 | Seiko Epson Corporation | Ink jet recording method, and ink jet recording apparatus |
JP5985350B2 (ja) * | 2012-10-24 | 2016-09-06 | サカタインクス株式会社 | インクセット及び印刷物 |
WO2014080942A1 (ja) * | 2012-11-20 | 2014-05-30 | サカタインクス株式会社 | 光硬化型インクジェット印刷用インク組成物及び印刷物 |
JP2016514174A (ja) | 2013-02-15 | 2016-05-19 | サン ケミカル コーポレイション | 低移行エネルギー硬化性インク |
JP6213164B2 (ja) * | 2013-11-06 | 2017-10-18 | セイコーエプソン株式会社 | 金属粉末、紫外線硬化型インクジェット組成物および記録物 |
JP6236471B2 (ja) * | 2014-01-31 | 2017-11-22 | 富士フイルム株式会社 | 建材印刷用インクジェットインク組成物、建材印刷用インクジェットインクセット、インクジェット記録方法、及び、加飾建材 |
JP6560505B2 (ja) * | 2015-02-26 | 2019-08-14 | サカタインクス株式会社 | 光硬化型インクジェット印刷用白色インク組成物 |
JP6900630B2 (ja) * | 2015-10-26 | 2021-07-07 | 株式会社リコー | 活性エネルギー線硬化型組成物、活性エネルギー線硬化型インク、組成物収容容器、2次元又は3次元の像の形成方法及び形成装置並びに成形加工品 |
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012126885A (ja) * | 2010-11-22 | 2012-07-05 | Seiko Epson Corp | 紫外線硬化型インクジェット用インク組成物 |
JP2012201847A (ja) * | 2011-03-28 | 2012-10-22 | Seiko Epson Corp | 紫外線硬化型インクジェット用インク組成物 |
JP2012255045A (ja) * | 2011-06-07 | 2012-12-27 | Seiko Epson Corp | 光硬化型インクジェット記録用インク組成物、インクジェット記録方法 |
US20150094394A1 (en) * | 2013-10-02 | 2015-04-02 | Samsung Electronics Co., Ltd. | Multi-color ink for 3d printing, 3d printer, and method of controlling the 3d printer |
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EP3911709A1 (en) | 2021-11-24 |
US20220073767A1 (en) | 2022-03-10 |
WO2020148441A1 (en) | 2020-07-23 |
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GB2580640B (en) | 2022-07-13 |
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