KR20110064367A - Photosensitive ink composition - Google Patents
Photosensitive ink composition Download PDFInfo
- Publication number
- KR20110064367A KR20110064367A KR1020090120929A KR20090120929A KR20110064367A KR 20110064367 A KR20110064367 A KR 20110064367A KR 1020090120929 A KR1020090120929 A KR 1020090120929A KR 20090120929 A KR20090120929 A KR 20090120929A KR 20110064367 A KR20110064367 A KR 20110064367A
- Authority
- KR
- South Korea
- Prior art keywords
- photosensitive
- ink composition
- weight
- capsule
- agent
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 95
- 239000002775 capsule Substances 0.000 claims abstract description 62
- -1 ultraviolet ray Substances 0.000 claims abstract description 27
- 239000002245 particle Substances 0.000 claims abstract description 26
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 25
- 239000011230 binding agent Substances 0.000 claims abstract description 21
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 20
- 239000002270 dispersing agent Substances 0.000 claims abstract description 19
- 239000012748 slip agent Substances 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 16
- 239000002904 solvent Substances 0.000 claims abstract description 14
- 230000004044 response Effects 0.000 claims abstract description 12
- 239000000853 adhesive Substances 0.000 claims abstract description 7
- 230000001070 adhesive effect Effects 0.000 claims abstract description 7
- 238000004062 sedimentation Methods 0.000 claims abstract description 7
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 5
- 239000000839 emulsion Substances 0.000 claims description 23
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 14
- 239000003921 oil Substances 0.000 claims description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 13
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 10
- 239000000049 pigment Substances 0.000 claims description 10
- 229920000728 polyester Polymers 0.000 claims description 9
- 239000000377 silicon dioxide Substances 0.000 claims description 9
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 8
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 8
- 239000004743 Polypropylene Substances 0.000 claims description 8
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 8
- 229920001155 polypropylene Polymers 0.000 claims description 8
- 239000003125 aqueous solvent Substances 0.000 claims description 7
- 150000002009 diols Chemical class 0.000 claims description 7
- 229920002647 polyamide Polymers 0.000 claims description 7
- 229920002635 polyurethane Polymers 0.000 claims description 7
- 239000004814 polyurethane Substances 0.000 claims description 7
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 229920001400 block copolymer Polymers 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- 229920001296 polysiloxane Polymers 0.000 claims description 6
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 claims description 5
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 claims description 5
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
- 239000004952 Polyamide Substances 0.000 claims description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 4
- 125000005442 diisocyanate group Chemical group 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 239000003112 inhibitor Substances 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 239000008096 xylene Substances 0.000 claims description 4
- 239000003849 aromatic solvent Substances 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims description 3
- 229920000058 polyacrylate Polymers 0.000 claims description 3
- 150000003512 tertiary amines Chemical class 0.000 claims description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims 4
- 229940095095 2-hydroxyethyl acrylate Drugs 0.000 claims 1
- 229940044192 2-hydroxyethyl methacrylate Drugs 0.000 claims 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 1
- 239000000976 ink Substances 0.000 description 80
- 238000003756 stirring Methods 0.000 description 22
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 150000003413 spiro compounds Chemical class 0.000 description 6
- 125000003003 spiro group Chemical group 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- WNXTZVMMNCCZTP-UHFFFAOYSA-N 2-hydroxyethyl 2-methylprop-2-enoate 5-hydroxy-2-methylpent-2-enoic acid Chemical compound OCCC=C(C(=O)O)C.C(C(=C)C)(=O)OCCO WNXTZVMMNCCZTP-UHFFFAOYSA-N 0.000 description 3
- IPGXHRDWHJEWBI-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate;4-hydroxy-2-methylidenebutanoic acid Chemical compound OCCOC(=O)C=C.OCCC(=C)C(O)=O IPGXHRDWHJEWBI-UHFFFAOYSA-N 0.000 description 3
- 108010010803 Gelatin Proteins 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- MIOPWDLAZRCMGE-UHFFFAOYSA-N butyl 2-methylprop-2-enoate 2-methylhept-2-enoic acid Chemical compound CCCCOC(=O)C(C)=C.CCCCC=C(C)C(O)=O MIOPWDLAZRCMGE-UHFFFAOYSA-N 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 235000019322 gelatine Nutrition 0.000 description 3
- 235000011852 gelatine desserts Nutrition 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 238000003801 milling Methods 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 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 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical group CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000010459 dolomite Substances 0.000 description 2
- 229910000514 dolomite Inorganic materials 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 229910052622 kaolinite Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 230000016776 visual perception Effects 0.000 description 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical group O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- XVEUJTIZHZIHJM-UHFFFAOYSA-N a828782 Chemical compound CCOC(N)=O.CCOC(N)=O XVEUJTIZHZIHJM-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229920005822 acrylic binder Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910001680 bayerite Inorganic materials 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001988 diarylethenes Chemical class 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical group CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- IQSHMXAZFHORGY-UHFFFAOYSA-N methyl prop-2-enoate;2-methylprop-2-enoic acid Chemical compound COC(=O)C=C.CC(=C)C(O)=O IQSHMXAZFHORGY-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 150000003658 tungsten compounds Chemical class 0.000 description 1
Classifications
-
- 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
- C09D11/50—Sympathetic, colour changing or similar inks
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
본 발명은, 자외선에 반응하여 색상을 발현하는 화합물이 캡슐화된 감광 캡슐과, 상기 감광 캡슐과 화학 반응하지 않는 용매와, 인쇄 대상물에 고착이 용이하도록 접착제 역할을 하는 바인더와, 감광 캡슐 입자들을 서로 분리시켜 상기 용매에 고루 분산시키기 위한 분산제와, 상기 감광 캡슐 입자들이 침강되는 것을 억제하기 위한 침강방지제와, 기포 발생을 억제하기 위한 소포제 및 마찰계수를 감소시키는 슬립제를 포함하는 감광성 잉크 조성물에 관한 것이다. 본 발명에 의하면, 감광 캡슐이 잉크 조성물 내에 고루 분산되어 매우 안정하고, 감광성 잉크 조성물을 인쇄 대상물에 인쇄하게 되면 감광 캡슐은 자외선 파장 대역의 차이에 따라 반응하여 색상을 발현한다.The present invention provides a photosensitive capsule in which a compound expressing color in response to ultraviolet rays is encapsulated, a solvent that does not chemically react with the photosensitive capsule, a binder serving as an adhesive to facilitate adhesion to a printed object, and photosensitive capsule particles. A photosensitive ink composition comprising a dispersant for separating and dispersing evenly in the solvent, an antisettling agent for inhibiting sedimentation of the photosensitive capsule particles, an antifoaming agent for suppressing bubble generation, and a slip agent for reducing a coefficient of friction will be. According to the present invention, the photosensitive capsule is uniformly dispersed in the ink composition and is very stable. When the photosensitive ink composition is printed on a printing object, the photosensitive capsule reacts according to the difference in the ultraviolet wavelength band to express color.
잉크, 감광 캡슐, 자외선, 바인더, 분산제, 침강방지제, 소포제, 슬립제 Ink, photosensitive capsule, ultraviolet ray, binder, dispersant, antisettling agent, antifoaming agent, slip agent
Description
본 발명은 잉크 조성물에 관한 것으로, 더욱 상세하게는 자외선에 반응하여 색상을 발현하는 감광성 잉크 조성물에 관한 것이다.The present invention relates to an ink composition, and more particularly to a photosensitive ink composition that expresses color in response to ultraviolet light.
광변색제는 빛을 흡수함으로써 색상 변화를 일으키는 물질로서, 최근까지 이러한 광변색제 및 그 현상에 대한 많은 연구가 이루어져 왔다. Photochromic agents are materials that cause color change by absorbing light. Until recently, many studies on photochromic agents and their phenomena have been made.
광변색 현상을 나타내는 화합물로는 사진의 감광제로 널리 사용되고 있는 할로겐화은을 비롯하여 스피로피란(Spiropyran), 스피로옥사진(Spirooxazine), 아조화합물(Azo compound), 디아릴에텐 등의 유기화합물과 텅스텐 화합물과 같은 무기 화합물 등이 있는 것으로 보고되고 있다. Compounds exhibiting photochromic phenomena include tungsten compounds, organic compounds such as silver halides that are widely used as photosensitizers, spiropyran, spiroxazine, azo compounds, and diarylethenes. It is reported that such inorganic compounds are present.
스피로계 화합물을 비롯한 여러 가지 유기 광변색제들은 그 자체로는 안정성이 낮을 뿐만 아니라, 일반적인 다른 유기화합물에 비하여 분자의 크기가 크기 때문에 물에 대한 용해도가 매우 낮아 거의 물에 용해되지 않을 뿐만 아니라 물에 분산되기도 어렵다. 특히, 스피로계 화합물은 그 합성이 어렵고 순도가 높은 화합물 을 얻기가 어려울 뿐만 아니라 가격도 비싸다는 단점이 있다. 그러나, 스피로계 화합물은 광감응이 매우 빨라 광변색 효과가 매우 크다는 장점이 있다. Various organic photochromic agents, including spiro compounds, are not only stable in themselves, but also have low solubility in water due to their large molecular size compared to other organic compounds. It is also difficult to disperse. In particular, the spiro compound is difficult to synthesize, and it is difficult to obtain a high purity compound, and also has a disadvantage that the price is expensive. However, the spiro compound has the advantage that the photosensitivity is very fast, the photochromic effect is very large.
따라서, 스피로계 화합물을 안정화시키고 내광성 향상을 위해 캡슐화하여 광변색제로 사용하려는 연구가 활발하게 이루어져 왔다. Therefore, studies have been actively made to stabilize the spiro compounds and use them as photochromic agents by encapsulating them for improving light resistance.
미합중국 특허 제5,017,225호는 마이크로캡슐화된 광변색 물질 및 그 제조방법에 대하여 개시하고 있다. US Patent No. 5,017,225 discloses microencapsulated photochromic materials and methods for their preparation.
또한, 대한민국 특허 제0127771호는 캡슐형 광변색제 조성물의 제조방법에 대하여 개시하고 있다. In addition, Korean Patent No. 0127771 discloses a method for preparing a capsule photochromic composition.
그러나, 미합중국 특허 제5,017,225호 및 대한민국 특허 제0127771호에 개시된 광변색제는 서로 엉켜서 덩어리지는 문제가 있으므로 코팅대상물에 전사하는데 어려움이 있다. 또한, 상기 광변색제를 수성 또는 유성 잉크에 적절히 고루 분산시키기가 어렵고, 광변색제를 잉크 조성물에 첨가하더라도 분자량이 커서 침강되어 버리기 때문에 이를 제어하기가 어려우며, 인쇄 대상물에 고착시켜 전사하는 데도 많은 어려움이 있고, 인쇄 후 인쇄 대상물은 고른 표면을 갖는 것이 바람직하지만 광변색제가 서로 덩어리져서 엉켜 있으므로 고른 표면을 얻기가 어렵다. However, the photochromic agents disclosed in U.S. Patent No. 5,017,225 and Korean Patent No. 0127771 have a problem that they are entangled with each other and are difficult to transfer to a coating object. In addition, it is difficult to properly disperse the photochromic agent in an aqueous or oily ink, and even if the photochromic agent is added to the ink composition, it is difficult to control because it has a large molecular weight, and it is difficult to control it. There is a difficulty, and after printing, the printed object preferably has an even surface, but it is difficult to obtain an even surface because the photochromic agents are agglomerated with one another.
본 발명이 이루고자 하는 기술적 과제는 감광 캡슐은 잉크 조성물 내에 고루 분산되어 매우 안정하고, 감광 캡슐의 침강을 억제할 수 있으며, 인쇄 대상물에 전사가 용이하고 인쇄 후 고른 표면을 얻을 수 있으며, 자외선에 반응하여 색상을 발현하는 감광성 잉크 조성물을 제공함에 있다. The technical problem to be achieved by the present invention is that the photosensitive capsule is uniformly dispersed in the ink composition, very stable, can suppress the settling of the photosensitive capsule, easy to transfer to the print object, obtain an even surface after printing, and reacts to ultraviolet rays By providing a photosensitive ink composition that expresses the color.
본 발명은, 자외선에 반응하여 색상을 발현하는 잉크 조성물에 있어서, 자외선에 반응하여 색상을 발현하는 화합물이 캡슐화된 감광 캡슐 20∼40중량%와, 상기 감광 캡슐과 화학 반응하지 않는 수성 용매 10∼30중량%와, 인쇄 대상물에 고착이 용이하도록 접착제 역할을 하는 바인더 40∼70중량%와, 감광 캡슐 입자들을 서로 분리시켜 상기 수성 용매에 고루 분산시키기 위한 분산제 0.1∼3중량%와, 상기 감광 캡슐 입자들이 침강되는 것을 억제하기 위한 침강방지제 0.1∼3중량%와, 기포 발생을 억제하기 위한 소포제 0.01∼3중량% 및 잉크 조성물의 마찰계수를 감소시키는 슬립제 0.1∼3중량%를 포함하며, 상기 잉크 조성물의 최대 입도가 5∼20㎛이고, 상기 잉크 조성물의 점도는 100∼1000 cps 범위를 갖는 감광성 잉크 조성물을 제공한다.In the ink composition which expresses color in response to ultraviolet rays, the present invention relates to 20 to 40% by weight of a photosensitive capsule in which a compound expressing color in response to ultraviolet light is encapsulated, and an aqueous solvent 10 to 10 that does not chemically react with the photosensitive capsule. 30 to 30% by weight, 40 to 70% by weight of a binder serving as an adhesive to easily adhere to a printing object, 0.1 to 3% by weight of a dispersant for separating the photosensitive capsule particles from each other and evenly dispersed in the aqueous solvent, and the photosensitive capsule 0.1 to 3% by weight of an antisettling agent for inhibiting sedimentation of particles, 0.01 to 3% by weight of antifoaming agent for suppressing bubble generation, and 0.1 to 3% by weight of slip agent for reducing the coefficient of friction of the ink composition, wherein It provides a photosensitive ink composition having a maximum particle size of the ink composition is 5 to 20㎛, the viscosity of the ink composition has a range of 100 to 1000 cps.
또한, 본 발명은, 자외선에 반응하여 색상을 발현하는 잉크 조성물에 있어서, 자외선에 반응하여 색상을 발현하는 화합물이 캡슐화된 감광 캡슐 20∼40중량% 와, 상기 감광 캡슐과 화학 반응하지 않는 유성 용매 30∼60중량%와, 인쇄 대상물에 고착이 용이하도록 접착제 역할을 하는 바인더 10∼20중량%와, 감광 캡슐 입자들을 서로 분리시켜 상기 유성 용매에 고루 분산시키기 위한 분산제 0.1∼3중량%와, 상기 감광 캡슐 입자들이 침강되는 것을 억제하기 위한 침강방지제 0.1∼3중량%와, 기포 발생을 억제하기 위한 소포제 0.01∼3중량% 및 잉크 조성물의 마찰계수를 감소시키는 슬립제 0.1∼3중량%를 포함하며, 상기 잉크 조성물의 최대 입도가 5∼20㎛이고, 상기 잉크 조성물의 점도는 500∼3000 cps 범위를 갖는 감광성 잉크 조성물을 제공한다.In addition, the present invention, in the ink composition to express the color in response to the ultraviolet light, 20 to 40% by weight of the photosensitive capsule in which the compound expressing the color in response to the ultraviolet light and the oil-based solvent that does not chemically react with the photosensitive capsule 30 to 60% by weight, 10 to 20% by weight of a binder acting as an adhesive to easily adhere to a printing object, and 0.1 to 3% by weight of a dispersant for separating the photosensitive capsule particles from each other and dispersing the oil solvent evenly. 0.1 to 3% by weight of an antisettling agent for inhibiting sedimentation of the photosensitive capsule particles, 0.01 to 3% by weight of an antifoaming agent for suppressing bubble generation, and 0.1 to 3% by weight of a slipping agent for reducing the coefficient of friction of the ink composition; The maximum particle size of the ink composition is 5 to 20 μm, and the viscosity of the ink composition provides a photosensitive ink composition having a range of 500 to 3000 cps.
상기 수성 용매는 물이고, 상기 바인더는 아크릴계 이멀젼(Emulsion) 또는 우레탄(urethane)계 이멀젼일 수 있다. The aqueous solvent is water, and the binder may be an acrylic emulsion or a urethane emulsion.
상기 아크릴계 이멀젼은 메틸메타아크릴레이트(Methylmethacrylate), 메틸아크릴레이트(Methylacrylate), 에틸아크릴레이트(Ethylacrylate), 노르말부틸아크릴레이트(n-Butylacrylate), 노르말부틸메타아크릴레이트(n-Butylmethacrylate), 에틸메타아크릴레이트(Ethylmethacrylate), 이소부틸메타아크릴레이트(iso-Butylmethacrylate), 메타아크릴산(Methacrylic Acid), 이소프로필메타아크릴레이트(iso-Propylmethacrylate), 2-에틸헥실아크릴레이트(2-Ethylhexylacrylate), 1,6-헥산디올디아크릴레이트(1,6-Hexanedioldiacrylate), 2-하이드록시에틸메타아크릴레이트(2-Hydroxyethylmethacrylate) 및 2-하이드록시에틸아크릴레이트(2-Hydroxyethylacrylate) 중에서 적어도 어느 하나의 모노머를 포함하는 이멀젼으로 이루어진 것일 수 있다. The acrylic emulsion is methyl methacrylate (Methylmethacrylate), methyl acrylate (Methylacrylate), ethyl acrylate (Ethylacrylate), normal butyl acrylate (n-Butylacrylate), normal butyl methacrylate (n-Butylmethacrylate), ethyl meth Ethylmethacrylate, isobutyl methacrylate, isocrymethic acid, methacrylic acid, isopropyl methacrylate, isopropylpropacrylate, 2-ethylhexyl acrylate, 1,6 Hexanediol diacrylate (1,6-Hexanedioldiacrylate), 2-hydroxyethyl methacrylate (2-Hydroxyethylmethacrylate) and 2-hydroxyethyl acrylate (2-Hydroxyethylacrylate) containing at least one monomer It may be composed of mullion.
상기 우레탄계 이멀젼은 디이소시아네이트 성분과 디올 성분과의 반응에 의해 얻어지는 우레탄계 중합체를 포함하는 것일 수 있다. The urethane-based emulsion may include a urethane-based polymer obtained by the reaction of a diisocyanate component and a diol component.
상기 유성 용매는 방향족 용매인 톨루엔(Tolune) 또는 자일렌(Xylene)이고, 상기 바인더는 아크릴(Acrylic)계, 폴리비닐(Polyvinyl)계, 폴리우레탄(Polyurethane)계, 폴리아미드(Polyamide)계, 에틸렌비닐아세테이트(EVA)계, 폴리에스테르(Polyester)계 또는 클로리네이티드 폴리프로필렌(Chlorinated Polypropylene)계 바인더일 수 있다. The oil solvent is toluene or xylene, which is an aromatic solvent, and the binder is acrylic, polyvinyl, polyurethane, polyamide, ethylene It may be a vinyl acetate (EVA) -based, polyester (polyester) -based or chlorinated polypropylene (Chlorinated Polypropylene) -based binder.
상기 분산제는 안료친화그룹을 가진 공중합체 용액으로 이루어진 것일 수 있다. The dispersant may be composed of a copolymer solution having a pigment affinity group.
상기 침강방지제는 실리카로 이루어진 것일 수 있다. The anti-settling agent may be made of silica.
상기 소포제는 폴리실록산계 소포제로 이루어진 것일 수 있다. The antifoaming agent may be made of a polysiloxane antifoaming agent.
상기 슬립제는 폴리에틸렌계, 폴리아마이드계, 폴리프로필렌계 또는 불소계 슬립제로 이루어진 것일 수 있다. The slip agent may be made of a polyethylene-based, polyamide-based, polypropylene-based or fluorine-based slip agent.
본 발명에 의한 감광성 잉크 조성물 및 그 제조방법에 의하면, 감광 캡슐은 잉크 조성물 내에 고루 분산되어 매우 안정하다. According to the photosensitive ink composition and the manufacturing method thereof according to the present invention, the photosensitive capsule is uniformly dispersed in the ink composition and is very stable.
또한, 감광 캡슐이 서로 엉켜 덩어리지는 현상이 억제되고, 잉크 조성물에 침강되는 현상도 억제할 수 있다. In addition, the phenomenon in which the photosensitive capsules are entangled with each other can be suppressed, and the phenomenon of settling in the ink composition can also be suppressed.
또한, 인쇄 대상물에 전사가 용이하고, 인쇄 후 인쇄 대상물은 고른 표면을 얻을 수 있다. In addition, transfer to the printing object is easy, and the printed object can be obtained with an even surface after printing.
감광 캡슐은 분자량이 크더라도, 감광성 유성 잉크 조성물은 종이나 필름 등의 인쇄 대상물에 그라비아(Gravure) 방식, 후렉소 방식(Flexo) 방식, 스크린(Screen) 방식 등의 다양한 인쇄 기법을 이용하여 인쇄할 수 있다. Although the photosensitive capsule has a large molecular weight, the photosensitive oil ink composition may be printed on a printing object such as paper or film using various printing techniques such as a gravure method, a flexo method, and a screen method. Can be.
또한, 감광 캡슐이 함유된 감광성 잉크 조성물을 인쇄 대상물에 인쇄하게 되면, 감광 캡슐은 자외선 파장 대역의 차이에 따라 반응하므로 이를 이용하여 자외선의 정도를 예측하는 것이 가능하다. In addition, when the photosensitive ink composition containing the photosensitive capsule is printed on an object to be printed, the photosensitive capsule reacts according to the difference in the ultraviolet wavelength band, and thus it is possible to predict the degree of ultraviolet rays using the photosensitive capsule.
이하, 본 발명에 따른 바람직한 실시예를 상세하게 설명하기로 한다. 그러나, 이하의 실시예는 이 기술분야에서 통상적인 지식을 가진 자에게 본 발명이 충분히 이해되도록 제공되는 것으로서 여러 가지 다른 형태로 변형될 수 있으며, 본 발명의 범위가 다음에 기술되는 실시예에 한정되는 것은 아니다. Hereinafter, preferred embodiments of the present invention will be described in detail. However, the following embodiments are provided to those skilled in the art to fully understand the present invention, and may be modified in various forms, and the scope of the present invention is limited to the embodiments described below. It doesn't happen.
감광성 잉크에 함유된 감광 캡슐에 자외선이 흡수됨으로써 발색하게 된다. 감광 캡슐은 자외선에 반응하여 색상을 발현하는 화합물이 캡슐화된 것이다. 색상은 흡수된 자외선의 양에 따라 그 발현 정도가 다르게 나타난다. Ultraviolet rays are absorbed by the photosensitive capsules contained in the photosensitive ink to develop colors. Photosensitive capsules are encapsulated compounds that express color in response to ultraviolet light. The color is expressed according to the amount of ultraviolet light absorbed.
자외선은 태양광의 일종으로서, 가시광선(400∼800㎚의 파장) 영역 중 파장이 가장 짧은 단파장 영역인 보라색 파장의 바깥쪽에 존재하는 태양광을 의미하며, 그 영역은 보통 200∼400㎚ 정도이다. 자외선 A(Ultra Violet-A; UV-A)는 320∼400㎚의 파장을 갖고, 자외선 B(UV-B)는 290∼320㎚의 파장을 가지며, 자외선 C(UV-C) 는 200∼290㎚의 파장을 갖는다.Ultraviolet rays are a kind of sunlight, which means sunlight existing outside the violet wavelength, which is the shortest wavelength in the visible light (wavelength of 400 to 800 nm) region, the region is usually about 200 to 400 nm. Ultraviolet A (Ultra Violet-A) has a wavelength of 320 to 400 nm, ultraviolet B (UV-B) has a wavelength of 290 to 320 nm, and ultraviolet C (UV-C) is 200 to 290 Has a wavelength of nm.
감광성 잉크는 특정한 영역의 자외선을 흡수함으로서 분자 구조가 변화하고, 이에 따라 가시광선의 발색을 하게 된다. 감광성 잉크의 발색은 특정 영역의 자외선의 존재를 의미하며, 자외선의 양이 많을수록 흡수량이 최대치에 가까워지므로 선명한 색상을 발색한다. The photosensitive ink absorbs ultraviolet rays in a specific area, thereby changing its molecular structure, thereby causing visible light to develop. Coloration of the photosensitive ink indicates the presence of ultraviolet light in a specific area, and the higher the amount of ultraviolet light, the closer the absorption amount is to a maximum, thereby producing a vivid color.
예컨대, 감광성 잉크가 파란색(Blue)과 빨간색(Red)을 발색하는 경우, 빨간색은 자외선 A 영역에서 발색하며, 파란색은 빨간색에 비하여 단파장인 자외선 B 영역에서 발색하게 된다. 이와 같이 파란색과 빨간색의 발색은 파장 대역의 차이가 있으므로 이를 이용하여 자외선의 정도를 예측하는 것이 가능하다. 감광성 잉크에 의한 파란색의 발색이 강한 경우에는 빨간색의 발색과 비교하여 더욱 강한 자외선이 존재한다는 것을 의미한다. For example, when the photosensitive ink develops blue and red, red color is developed in the ultraviolet A region, and blue color is developed in the ultraviolet B region having a shorter wavelength than red. As described above, since blue and red colors have different wavelength bands, it is possible to predict the degree of ultraviolet rays by using the same. In the case where the color of the blue color by the photosensitive ink is strong, it means that there is a stronger ultraviolet light than the color of the red color.
<감광 캡슐><Photosensitive capsule>
감광 캡슐은 다음과 같은 과정을 통하여 얻을 수 있다. Photosensitive capsules can be obtained through the following process.
광변색 현상을 일으키는 화합물로는 스피로피란(Spiropyran), 스피로옥사진(Spirooxazine)과 같은 스피로계 화합물을 사용할 수 있다. 이러한 스피로계 화합물은 안정성이 낮을 뿐 아니라, 일반적인 다른 유기화합물에 비하여 어느 정도 분자의 크기가 크기 때문에 물에 대한 용해도가 매우 낮아 거의 물에 용해되지 않고, 또한 물에 분산되기도 어렵다는 단점이 있으나, 광감응이 매우 빨라 광변색 효과가 매우 크다는 장점이 있다. As the compound causing the photochromic phenomenon, spiro-based compounds such as spiropyran and spiroxazine may be used. These spiro compounds are not only low in stability, but also have a disadvantage in that they are hardly soluble in water and difficult to disperse in water due to their large solubility in water compared to other organic compounds. It is very quick to respond, so the photochromic effect is very large.
스피로계 화합물은 다음의 구조식을 갖는다. Spiro compounds have the following structural formula.
상기 구조식에서, 상기 R1은 수소, 메톡시나 에톡기 등과 같은 알콕시, 할로겐원자 또는 트리플루오로메틸이고, R2는 수소 또는 메틸기나 에틸기 등과 같은 알킬기이며, R3는 수소, 디메틸아민 또는 디에틸아민 등과 같은 아민, 피페리딘 또는 몰포린(molpholine)이고, R4는 수소, 메톡시나 에톡시 등과 같은 알콕시 또는 할로겐원자이며, X는 탄소(스피로피란계) 또는 질소(스피로옥사진계)이고, Y는 산소 또는 황이고, A는 벤젠 또는 나프탈렌 등과 같은 방향족 고리 화합물이고, B는 벤젠 또는 나프탈렌 등과 같은 방향족 고리 화합물 또는 헤테로고리 화합물이다. In the above structural formula, R1 is alkoxy, halogen atom or trifluoromethyl such as hydrogen, methoxy or ethoxy group, R2 is hydrogen or alkyl group such as methyl or ethyl group, R3 is hydrogen, dimethylamine or diethylamine etc. Is an amine, piperidine or molpholine, R 4 is hydrogen, an alkoxy or halogen atom such as methoxy or ethoxy, X is carbon (spiropyrane) or nitrogen (spirooxazine), and Y is Oxygen or sulfur, A is an aromatic ring compound such as benzene or naphthalene, and B is an aromatic ring compound or heterocyclic compound such as benzene or naphthalene, and the like.
감광 캡슐을 얻기 위하여, 먼저 스피로피란(Spiropyran), 스피로옥사진(Spirooxazine)과 같은 스피로계 화합물을 첨가제와 함께 오일에 가열하여 용해시켜 스피로계 용액을 준비한다. 물이 담긴 용기를 가열하고 젤라틴(또는 멜라민)을 상기 물이 담긴 용기에 첨가하여 용해시킨 젤라틴(또는 멜라민) 용액을 준비한다. In order to obtain a photosensitive capsule, a spiro-based solution is prepared by first dissolving a spiro-based compound such as Spiropyran and Spirooxazine in an oil with an additive. Heat the vessel containing water and add gelatin (or melamine) to the vessel containing water to prepare a dissolved gelatin (or melamine) solution.
상기 젤라틴(또는 멜라민) 용액을 교반기를 이용하여 교반하면서 상기 스피로계 용액을 적하시켜 에멀젼을 형성시키고, 계속 교반하면서 상기 교반기에 코팅용 수지를 가하여 유화된 입자들을 코팅용 수지로 코팅시킨다. 이렇게 코팅용 수지로 코팅되어 얻어진 감광 캡슐은 매우 안정하여 여러 가지 형태의 도료, 잉크 또는 안료 등에 사용될 수 있다. 감광 캡슐은 내화학성, 내약품성 등을 가지며 화학적 안정성이 높다. While stirring the gelatin (or melamine) solution using a stirrer, the spiro-based solution is added dropwise to form an emulsion, while continuing stirring to add a coating resin to the stirrer to coat the emulsified particles with a coating resin. The photosensitive capsule obtained by coating with a resin for coating is very stable and can be used in various types of paints, inks or pigments. The photosensitive capsule has chemical resistance, chemical resistance and the like and has high chemical stability.
상기 감광 캡슐은 광변색 현상을 일으키는 스피로계 화합물을 그 예로 들어 설명하였으나, 스피로계 화합물 이외에도 광변색 현상을 일으키는 다양한 화합물을 포함하는 감광 캡슐로 이루어질 수도 있다. 이러한 감광 캡슐은 수성 잉크 조성물 또는 유성 잉크 조성물에 함유되어 자외선에 반응하여 색상을 발현하는 감광성 잉크 조성물을 구현할 수 있다. The photosensitive capsule has been described with reference to a spiro-based compound causing a photochromic phenomenon, it may be made of a photosensitive capsule containing a variety of compounds that cause a photochromic phenomenon in addition to the spiro-based compound. Such a photosensitive capsule may be included in an aqueous ink composition or an oily ink composition to implement a photosensitive ink composition that expresses color in response to ultraviolet rays.
<감광성 수성 잉크 조성물><Photosensitive aqueous ink composition>
이하에서, 본 발명의 바람직한 실시 예에 따른 감광성 수성 잉크 조성물에 대하여 설명한다. Hereinafter, a photosensitive aqueous ink composition according to a preferred embodiment of the present invention will be described.
교반기에 수성 용매인 물과 이멀젼(Emulsion)을 투입하여 교반한다. 교반기의 교반속도는 800∼1500 rpm 정도인 것이 바람직하다. Water and emulsion, which are aqueous solvents, are added to the stirrer and stirred. It is preferable that the stirring speed of a stirrer is about 800-1500 rpm.
상기 물은 감광성 잉크 조성물의 점도, 인쇄 후의 자외선에 대한 발색 정도 등을 고려하여 감광성 잉크 조성물의 총량에 대하여 10∼30중량% 첨가하는 것이 바람직하다. It is preferable to add 10-30 weight% of said water with respect to the total amount of the photosensitive ink composition in consideration of the viscosity of the photosensitive ink composition, the degree of color development with respect to the ultraviolet-ray after printing, etc.
상기 이멀젼은 감광성 잉크 조성물 및 이에 함유된 감광 캡슐이 종이나 필름 등의 인쇄 대상물에 고착될 수 있도록 하는 접착제 역할을 한다. 상기 이멀젼으로는 아크릴계 이멀젼(Emulsion) 또는 우레탄(urethane)계 이멀젼을 사용할 수 있다. 상기 아크릴계 이멀젼(Emulsion) 또는 우레탄(urethane)계 이멀젼은 감광성 잉크 조성물의 점도 등을 고려하여 감광성 잉크 조성물의 총량에 대하여 40∼70중량% 첨가하는 것이 바람직하다. The emulsion serves as an adhesive to allow the photosensitive ink composition and the photosensitive capsule contained therein to adhere to a printing object such as paper or film. As the emulsion, an acrylic emulsion (emulsion) or a urethane (urethane) emulsion may be used. The acrylic emulsion or urethane emulsion is preferably added in an amount of 40 to 70 wt% based on the total amount of the photosensitive ink composition in consideration of the viscosity of the photosensitive ink composition.
상기 아크릴계 이멀젼은 메틸메타아크릴레이트(Methylmethacrylate), 메틸아크릴레이트(Methylacrylate), 에틸아크릴레이트(Ethylacrylate), 노르말부틸아크릴레이트(n-Butylacrylate), 노르말부틸메타아크릴레이트(n-Butylmethacrylate), 에틸메타아크릴레이트(Ethylmethacrylate), 이소부틸메타아크릴레이트(iso-Butylmethacrylate), 메타아크릴산(Methacrylic Acid), 이소프로필메타아크릴레이트(iso-Propylmethacrylate), 2-에틸헥실아크릴레이트(2-Ethylhexylacrylate), 1,6-헥산디올디아크릴레이트(1,6-Hexanedioldiacrylate), 2-하이드록시에틸메타아크릴레이트(2-Hydroxyethylmethacrylate) 및 2-하이드록시에틸아크릴레이트(2-Hydroxyethylacrylate) 중에서 적어도 어느 하나의 모노머(Monomer)를 포함하는 아크릴계 화합물에 물이 혼합된 용액일 수 있다. 상기 아크릴계 이멀젼은 아크릴계 화합물이 30∼50중량% 함유되고, 물이 50∼70중량% 함유되어 있는 것이 바람직하다.The acrylic emulsion is methyl methacrylate (Methylmethacrylate), methyl acrylate (Methylacrylate), ethyl acrylate (Ethylacrylate), normal butyl acrylate (n-Butylacrylate), normal butyl methacrylate (n-Butylmethacrylate), ethyl meth Ethylmethacrylate, isobutyl methacrylate, isocrymethic acid, methacrylic acid, isopropyl methacrylate, isopropylpropacrylate, 2-ethylhexyl acrylate, 1,6 -At least one monomer of hexanediol diacrylate (1,6-Hexanedioldiacrylate), 2-hydroxyethyl methacrylate (2-Hydroxyethylmethacrylate) and 2-hydroxyethyl acrylate (2-Hydroxyethylacrylate) It may be a solution in which water is mixed with an acryl-based compound. It is preferable that the said acrylic emulsion contains 30-50 weight% of acrylic compounds, and contains 50-70 weight% of water.
상기 우레탄계 이멀젼은 디이소시아네이트 성분과 디올 성분과의 반응에 의해 얻어지는 우레탄계 중합체를 포함할 수 있다. 상기 디이소시아네이트 성분은 페 닐렌 디이소시아네이트, 톨릴렌 디이소시아네이트, 디페닐디탄-4,4'-디이소시아네이트, 크실릴렌 디이소시아네이트, 이소포론 디이소시아네이트, 1,6-헥사메틸렌 디이소시아네이트, 리신 디이소시아네이트 등일 수 있다. 상기 디올 성분은 폴리에스테르 디올, 폴리에테르 디올, 폴리카르보네이트 디올 등일 수 있다. 상기 우레탄계 이멀젼은 우레탄계 중합체가 30∼50중량% 함유되고, 물이 50∼70중량% 함유되어 있는 것이 바람직하다. The urethane-based emulsion may include a urethane-based polymer obtained by the reaction of the diisocyanate component and the diol component. The diisocyanate component is phenylene diisocyanate, tolylene diisocyanate, diphenylditan-4,4'-diisocyanate, xylylene diisocyanate, isophorone diisocyanate, 1,6-hexamethylene diisocyanate, lysine diisocyanate And the like. The diol component may be polyester diol, polyether diol, polycarbonate diol, or the like. It is preferable that the said urethane type emulsion contains 30-50 weight% of urethane polymers, and contains 50 to 70 weight% of water.
상기 교반기를 교반하면서 안료친화그룹을 가진 공중합체 용액 분산제를 투입한다. 상기 분산제는, 예컨대 카르복실릭산을 안료친화그룹으로 갖는 폴리아크릴레이트 블록공중합체 용액일 수 있다. 상기 분산제는 감광 캡슐 입자들을 분리시켜 서로 뭉치는 현상을 억제하는 역할을 한다. 상기 분산제는 감광성 잉크 조성물의 총량에 대하여 0.1∼3중량% 첨가하는 것이 바람직하다. While stirring the stirrer, a copolymer solution dispersant having a pigment affinity group was added thereto. The dispersant may be, for example, a polyacrylate block copolymer solution having carboxylic acid as the pigment affinity group. The dispersant separates the photosensitive capsule particles and serves to suppress agglomeration. It is preferable to add 0.1 to 3 weight% of said dispersing agent with respect to the total amount of the photosensitive ink composition.
상기 교반기를 교반하면서 감광 캡슐을 투입한다. 상기 감광 캡슐은 감광성 잉크 조성물의 총량에 대하여 20∼40중량% 첨가하는 것이 바람직하다. 감광 캡슐의 첨가량은 너무 적을 경우 시각적으로 색변화를 인지할 수 있는 정도가 약하게 되어 감광 변색 효과가 떨어질 수 있고, 감광 캡슐의 첨가량이 너무 많을 경우 잉크의 인쇄가 잘 되지 않거나 하는 등의 인쇄 불량이 발생할 수 있다. The photosensitive capsule is added while stirring the stirrer. It is preferable to add 20-40 weight% of the said photosensitive capsule with respect to the total amount of the photosensitive ink composition. If the amount of the photosensitive capsule is too small, the degree of visual perception of color change is weak, and the photochromic effect may be reduced. If the amount of the photosensitive capsule is too large, the printing defects such as ink may not be printed well. May occur.
상기 교반기를 교반하면서 침강방지제, 소포제, 슬립제와 같은 첨가제를 투입한다. While stirring the stirrer, additives such as a sedimentation inhibitor, an antifoaming agent, and a slipping agent are added.
상기 침강방지제는 감광성 잉크 조성물을 구성하는 입자들이 침강되는 현상을 억제하기 위하여 첨가한다. 상기 침강방지제는 실리카(Silica), 알루미나, 카올 리나이트, 벤토나이트, 돌로마이트, 바이어라이트(BaSO4), 칼슘카보네이트(CaCO3), 탈크, 티타니아, 규조토 등의 무기물을 사용할 수 있는데, 감광성 잉크 조성물은 빛에 대한 반응성이 요구되므로 실리카(Silica)와 같은 투명한 실리콘(Silicon)계 침강방지제를 사용하는 것이 바람직하다. 상기 침강방지제는 감광성 잉크 조성물의 총량에 대하여 0.1∼3중량% 첨가하는 것이 바람직하다. The antisettling agent is added to suppress the phenomenon that the particles constituting the photosensitive ink composition is settled. The anti-settling agent may be used inorganic materials such as silica, alumina, kaolinite, bentonite, dolomite, vialite (BaSO 4 ), calcium carbonate (CaCO 3 ), talc, titania, diatomaceous earth, and the like. Since reactivity to light is required, it is preferable to use a transparent silicon-based anti-settling agent such as silica. It is preferable to add 0.1 to 3 weight% of said anti-settling agent with respect to the total amount of the photosensitive ink composition.
상기 소포제는 분산시 또는 인쇄시 기포가 발생할 수 있으며, 기포 발생을 억제하거나 기포로 인해 인쇄시 핀홀이 생기는 현상을 억제하기 위하여 첨가한다. 상기 소포제는 폴리실록산(Polysiloxane)계 소포제를 사용할 수 있다. 상기 소포제는 감광성 잉크 조성물의 총량에 대하여 0.01∼3중량% 첨가하는 것이 바람직하다. The antifoaming agent may generate bubbles at the time of dispersion or printing, and is added to suppress the generation of bubbles or to suppress the occurrence of pinholes during printing due to the bubbles. The antifoaming agent may be a polysiloxane antifoaming agent. It is preferable to add 0.01 to 3 weight% of said antifoamers with respect to the total amount of the photosensitive ink composition.
상기 슬립제는 감광성 잉크 조성물의 겔화 현상을 방지하고, 마찰계수를 감소시켜 인쇄 후 마찰에 의해 잉크가 묻어나오지 않게 하기 위하여 첨가한다. 상기 슬립제는 폴리에틸렌(Polyethylene)계, 폴리아마이드(Polyamide)계 또는 불소(Fluorine)계 슬립제를 사용할 수 있다. 상기 슬립제는 감광성 잉크 조성물의 총량에 대하여 0.1∼3중량% 첨가하는 것이 바람직하다. The slip agent is added to prevent gelation of the photosensitive ink composition and to reduce the coefficient of friction so that ink does not come out by friction after printing. The slip agent may be a polyethylene, polyamide, or fluorine slip agent. It is preferable that the said slip agent is added 0.1 to 3 weight% with respect to the total amount of the photosensitive ink composition.
이렇게 얻어진 감광성 잉크 조성물은 그 입도가 5∼20㎛ 정도이다. 상기 감광성 잉크 조성물은 그 점도가 100∼1000 cps(centi poise) 정도이다. The photosensitive ink composition thus obtained has a particle size of about 5 to 20 µm. The photosensitive ink composition has a viscosity of about 100 to 1000 cps (centi poise).
감광성 수성 잉크 조성물은 종이나 필름 등의 인쇄 대상물에 그라비아(Gravure) 방식, 후렉소(Flexo) 방식 등의 다양한 인쇄 기법을 이용하여 인쇄할 수 있다. 감광성 수성 잉크 조성물이 인쇄 대상물에 인쇄되고, 인쇄 대상물이 자외 선을 받게 되면 감광 캡슐에 포함된 발색제에 의해 파란색, 빨간색 등의 유색으로 발색하게 된다. The photosensitive aqueous ink composition may be printed on a printing object such as paper or film using various printing techniques such as a gravure method, a flexo method, and the like. When the photosensitive aqueous ink composition is printed on a print object and the print object receives ultraviolet rays, the photosensitive aqueous ink composition is colored in a color such as blue or red by a colorant included in the photosensitive capsule.
<감광성 유성 잉크 조성물><Photosensitive oil ink composition>
이하에서는, 본 발명의 바람직한 실시예에 따른 감광성 유성 잉크 조성물에 대하여 설명한다. Hereinafter, a photosensitive oil ink composition according to a preferred embodiment of the present invention will be described.
교반기에 유성 용매와 바인더(binder)를 투입하여 교반한다. 교반기의 교반속도는 800∼1500 rpm 정도인 것이 바람직하다. An oily solvent and a binder are added to the stirrer and stirred. It is preferable that the stirring speed of a stirrer is about 800-1500 rpm.
유성 용매로는 하이드로 카본계 용매를 사용할 수 있는데, 상기 하이드로 카본계 용매에는 방향족 용매인 톨루엔(Tolune), 자일렌(Xylene) 등이 있다. 메틸에틸케톤(MEK), 디아세톤알콜(DAA) 등과 같은 케톤계 용매를 사용할 경우, 감광 캡슐이 녹을 수 있으므로 사용하지 않는 것이 바람직하다. 상기 용매는 감광성 잉크 조성물의 점도, 인쇄 후의 자외선에 대한 발색 정도 등을 고려하여 감광성 잉크 조성물의 총량에 대하여 30∼60중량% 첨가하는 것이 바람직하다. Hydrocarbon-based solvents may be used as the oil-based solvent. The hydrocarbon-based solvents include toluene, xylene, and the like, which are aromatic solvents. When using a ketone solvent such as methyl ethyl ketone (MEK), diacetone alcohol (DAA), etc., it is preferable not to use the photosensitive capsule because it may melt. It is preferable to add 30-60 weight% of the said solvent with respect to the total amount of the photosensitive ink composition in consideration of the viscosity of the photosensitive ink composition, the degree of color development with respect to the ultraviolet-ray after printing, etc.
상기 바인더는 감광성 잉크 조성물 및 이에 함유된 감광 캡슐이 종이나 필름 등의 인쇄 대상물에 고착될 수 있도록 하는 접착제 역할을 한다. 바인더는 아크릴(Acrylic)계, 폴리비닐(Polyvinyl)계, 에틸렌비닐아세테이트(EVA)계, 폴리에스테르(Polyester)계, 폴리우레탄(Polyurethane)계, 폴리아미드(Polyamide)계 또는 폴리프로필렌(Polypropylene)계 바인더를 사용할 수 있다. 상기 바인더는 감광성 잉크 조성물의 점도 등을 고려하여 감광성 잉크 조성물의 총량에 대하여 10∼20중량% 첨가하는 것이 바람직하다. The binder serves as an adhesive to allow the photosensitive ink composition and the photosensitive capsule contained therein to adhere to a printing object such as paper or film. The binder is acrylic, polyvinyl, ethylene vinyl acetate, EVA, polyester, polyurethane, polyamide, or polypropylene. A binder can be used. The binder is preferably added in an amount of 10 to 20% by weight based on the total amount of the photosensitive ink composition in consideration of the viscosity of the photosensitive ink composition and the like.
상기 아크릴계 바인더는 메틸메타아크릴레이트(Methylmethacrylate), 메틸아크릴레이트(Methylacrylate), 에틸아크릴레이트(Ethylacrylate), 노르말부틸아크릴레이트(n-Butylacrylate), 노르말부틸메타아크릴레이트(n-Butylmethacrylate), 에틸메타아크릴레이트(Ethylmethacrylate), 이소부틸메타아크릴레이트(iso-Butylmethacrylate), 메타아크릴산(Methacrylic Acid), 이소프로필메타아크릴레이트(iso-Propylmethacrylate), 2-에틸헥실아크릴레이트(2-Ethylhexylacrylate), 1,6-헥산디올디아크릴레이트(1,6-Hexanedioldiacrylate), 2-하이드록시에틸메타아크릴레이트(2-Hydroxyethylmethacrylate) 및 2-하이드록시에틸아크릴레이트(2-Hydroxyethylacrylate) 중에서 적어도 어느 하나의 모노머(Monomer)를 포함하는 바인더일 수 있다. The acrylic binder is methyl methacrylate (Methylmethacrylate), methyl acrylate (Methylacrylate), ethyl acrylate (Ethylacrylate), normal butyl acrylate (n-Butylacrylate), normal butyl methacrylate (n-Butylmethacrylate), ethyl methacryl Ethylmethacrylate, isobutylmethacrylate, methacrylic acid, isopropylmethacrylate, isopropylpropacrylate, 2-ethylhexylacrylate, 1,6- At least one monomer of hexanediol diacrylate (1,6-Hexanedioldiacrylate), 2-hydroxyethyl methacrylate (2-Hydroxyethylmethacrylate) and 2-hydroxyethyl acrylate (2-Hydroxyethylacrylate) is included It may be a binder.
상기 프로필렌계 바인더는 크롤리네이티드 폴리프로필렌(Chlorinated PolyPropylene; CPP) 일 수 있다. The propylene-based binder may be chlorinated polypropylene (CPP).
상기 교반기를 교반하면서 안료친화그룹을 가진 공중합체 용액 분산제를 투입한다. 상기 분산제는, 예컨대 3급아민을 안료친화그룹으로 갖는 폴리에스터/폴리우레탄 블록공중합체 용액일 수 있다. 상기 분산제는 감광 캡슐 입자들을 분리시켜 서로 뭉치는 현상을 억제하는 역할을 한다. 상기 분산제는 감광성 잉크 조성물의 총량에 대하여 0.1∼3중량% 첨가하는 것이 바람직하다. While stirring the stirrer, a copolymer solution dispersant having a pigment affinity group was added thereto. The dispersant may be, for example, a polyester / polyurethane block copolymer solution having a tertiary amine as a pigment affinity group. The dispersant separates the photosensitive capsule particles and serves to suppress agglomeration. It is preferable to add 0.1 to 3 weight% of said dispersing agent with respect to the total amount of the photosensitive ink composition.
상기 교반기를 교반하면서 파우더(Powder) 상태의 감광 캡슐을 투입한다. 상기 감광 캡슐은 감광성 잉크 조성물의 총량에 대하여 20∼40중량% 첨가하는 것이 바람직하다. 감광 캡슐의 첨가량은 너무 적을 경우 시각적으로 색변화를 인지할 수 있는 정도가 약하게 되어 감광 변색 효과가 떨어질 수 있고, 감광 캡슐의 첨가량이 너무 많을 경우 잉크의 인쇄가 잘 되지 않거나 하는 등의 인쇄 불량이 발생할 수 있다. While stirring the stirrer, a photosensitive capsule in a powder state is introduced. It is preferable to add 20-40 weight% of the said photosensitive capsule with respect to the total amount of the photosensitive ink composition. If the amount of the photosensitive capsule is too small, the degree of visual perception of color change is weak, and the photochromic effect may be reduced. If the amount of the photosensitive capsule is too large, the printing defects such as ink may not be printed well. May occur.
상기 교반기를 교반하면서 침강방지제, 소포제, 슬립제와 같은 첨가제를 투입한다. While stirring the stirrer, additives such as a sedimentation inhibitor, an antifoaming agent, and a slipping agent are added.
상기 침강방지제는 감광성 잉크 조성물을 구성하는 입자들이 침강되는 현상을 억제하기 위하여 첨가한다. 상기 침강방지제는 실리카(Silica), 알루미나, 카올리나이트, 벤토나이트, 돌로마이트, 바이어라이트(BaSO4), 칼슘카보네이트(CaCO3), 탈크, 티타니아, 규조토 등의 무기물을 사용할 수 있는데, 감광성 잉크 조성물은 빛에 대한 반응성이 요구되므로 실리카(Silica)와 같은 투명한 실리콘(Silicon)계 침강방지제를 사용하는 것이 바람직하다. 상기 침강방지제는 감광성 잉크 조성물의 총량에 대하여 0.1∼3중량% 첨가하는 것이 바람직하다. The antisettling agent is added to suppress the phenomenon that the particles constituting the photosensitive ink composition is settled. The anti-settling agent may be used an inorganic material such as silica (Silica), alumina, kaolinite, bentonite, dolomite, Bayerite (BaSO 4 ), calcium carbonate (CaCO 3 ), talc, titania, diatomaceous earth, the photosensitive ink composition to light Since reactivity is required, it is preferable to use a transparent silicon-based anti-settling agent such as silica. It is preferable to add 0.1 to 3 weight% of said anti-settling agent with respect to the total amount of the photosensitive ink composition.
상기 소포제는 분산시 또는 인쇄시 기포가 발생할 수 있으며, 기포 발생을 억제하거나 기포로 인해 인쇄시 핀홀이 생기는 현상을 억제하기 위하여 첨가한다. 상기 소포제는 폴리실록산(Polysiloxane)계 소포제를 사용할 수 있다. 상기 소포제는 감광성 잉크 조성물의 총량에 대하여 0.01∼3중량% 첨가하는 것이 바람직하다. The antifoaming agent may generate bubbles at the time of dispersion or printing, and is added to suppress the generation of bubbles or to suppress the occurrence of pinholes during printing due to the bubbles. The antifoaming agent may be a polysiloxane antifoaming agent. It is preferable to add 0.01 to 3 weight% of said antifoamers with respect to the total amount of the photosensitive ink composition.
상기 슬립제는 감광성 잉크 조성물의 마찰계수를 감소시켜 인쇄 후 마찰에 의해 잉크가 묻어나오지 않게 하기 위하여 첨가한다. 상기 슬립제는 폴리에틸 렌(Polyethylene)계 또는 불소(Fluorine)계 슬립제를 사용할 수 있다. 상기 슬립제는 감광성 잉크 조성물의 총량에 대하여 0.1∼3중량% 첨가하는 것이 바람직하다. The slip agent is added to reduce the coefficient of friction of the photosensitive ink composition so that ink does not come out by friction after printing. The slip agent may be a polyethylene or fluorine slip agent. It is preferable that the said slip agent is added 0.1 to 3 weight% with respect to the total amount of the photosensitive ink composition.
감광 잉크 조성물의 입도를 조절하고, 감광 캡슐이 서로 엉키는 것을 억제하여 감광 잉크 조성물에 고루 분산되도록 하기 위하여 밀링(Milling) 공정을 수행한다. 밀링 공정은 적어도 2개, 바람직하게는 3개의 롤(Roll)을 이용하여 감광 잉크 조성물을 압착하여 수행하고, 이에 의해 필요한 정도의 입도 및 분산 효과를 얻을 수 있다. A milling process is performed to adjust the particle size of the photosensitive ink composition and to prevent the photosensitive capsules from tangling with each other and to be evenly dispersed in the photosensitive ink composition. The milling process is carried out by pressing the photosensitive ink composition using at least two, preferably three rolls, thereby obtaining the required particle size and dispersion effect.
이렇게 얻어진 감광성 잉크 조성물은 그 입도가 5∼20㎛ 정도이다. 상기 감광성 잉크 조성물은 그 점도가 500∼3000 cps(centi poise) 정도이다. The photosensitive ink composition thus obtained has a particle size of about 5 to 20 µm. The photosensitive ink composition has a viscosity of about 500 to 3000 cps (centi poise).
감광성 유성 잉크 조성물은 종이나 필름 등의 인쇄 대상물에 그라비아(Gravure) 방식, 스크린(Screen) 방식 등의 다양한 인쇄 기법을 이용하여 인쇄할 수 있다. 감광성 유성 잉크 조성물이 인쇄 대상물에 인쇄되고, 인쇄 대상물이 자외선을 받게 되면 감광 캡슐에 포함된 발색제(광변색 현상을 일으키는 화합물)에 의해 파란색, 빨간색 등의 유색으로 발색하게 된다. The photosensitive oil ink composition may be printed on a printing object such as paper or film using various printing techniques such as a gravure method and a screen method. When the photosensitive oil ink composition is printed on a printing object, and the printing object receives ultraviolet rays, the photosensitive oil ink composition is colored in a color such as blue or red by a colorant (compound causing photochromic phenomenon) included in the photosensitive capsule.
<실시예 1>≪ Example 1 >
교반기에 물 3g과 아크릴계 이멀젼(Emulsion)인 메틸아크릴레이트 63g을 투입하여 교반한다. 이때, 교반기는 800 rpm의 교반 속도로 설정하여 교반한다. 3g of water and 63g of methyl acrylate, which is an acrylic emulsion, are added to the stirrer and stirred. At this time, the stirrer is stirred at a stirring speed of 800 rpm.
이때 조성물의 온도는 10∼35℃ 범위, 교반 시간은 5∼10분이 적당하다.At this time, the temperature of the composition is 10 to 35 ℃ range, the stirring time is 5 to 10 minutes are suitable.
상기 메틸아크릴레이트(Methylacrylate)는 메틸아크릴레이트가 50중량% 함유 되고, 물이 50중량% 함유되어 있는 것이다. The methyl acrylate (Methylacrylate) is a 50% by weight of methyl acrylate, 50% by weight of water is contained.
상기 교반기를 교반하면서 분산제로 카르복실릭산을 안료친화그룹으로 갖는 폴리아크릴레이트 블록공중합체 용액을 1g 투입한다. 상기 교반기를 교반하면서 감광 캡슐 30g을 투입한다. 이때 교반기는 1000∼1300 rpm의 교반속도로 설정하고, 온도는 10∼35℃ 범위 내에서 교반 시간은 10∼30분 정도로 한다.While stirring the stirrer, 1 g of a polyacrylate block copolymer solution having carboxylic acid as a pigment affinity group was added as a dispersant. 30 g of photosensitive capsules are added while stirring the stirrer. At this time, the stirrer is set at a stirring speed of 1000 to 1300 rpm, and the temperature is set to about 10 to 30 minutes with a stirring time within a range of 10 to 35 ° C.
상기 교반기를 교반하면서 침강방지제인 실리카(Silica) 1g, 폴리시록산계 소포제 1g, 폴리에틸렌계 슬립제 1g을 투입하여 감광성 수성 잉크 조성물을 얻는다. While stirring the stirrer, 1 g of silica, a polysiloxane antifoaming agent, 1 g of polyethylene anti-slip agent 1 g is added to obtain a photosensitive aqueous ink composition.
<실시예 2><Example 2>
교반기에 톨루엔 40g과 바인더인 폴리비닐클로라이드 8g, 폴리프로필렌 8g을 투입하여 교반한다. 이때, 교반기는 1000∼1300 rpm의 교반 속도로 설정하여 바인더가 완전히 용해될 때까지 10∼30분 정도 교반한다. 40 g of toluene, 8 g of polyvinyl chloride as a binder, and 8 g of polypropylene were added to the stirrer and stirred. At this time, the stirrer is set at a stirring speed of 1000 to 1300 rpm and stirred for about 10 to 30 minutes until the binder is completely dissolved.
상기 교반기를 교반하면서 분산제로 3급 아민을 안료친화그룹으로 갖는 폴리에스터/폴리우레탄 블록공중합체 용액을 1g 투입한다. 상기 교반기를 교반하면서 감광 캡슐 40g을 투입한다. 이때 교반기는 800∼1000rpm의 교반속도로 설정하고 온도는 10∼35℃의 범위에서 교반한다.While stirring the stirrer, 1 g of a polyester / polyurethane block copolymer solution having a tertiary amine as a pigment affinity group was added as a dispersant. 40 g of photosensitive capsules are added while stirring the stirrer. At this time, the stirrer is set at a stirring speed of 800 to 1000 rpm and the temperature is stirred in the range of 10 to 35 ° C.
상기 교반기를 교반하면서 침강방지제인 실리카(Silica) 1g, 폴리실록산계 소포제 1g, 폴리에틸렌계 슬립제 1g을 투입한다. While stirring the stirrer, 1 g of silica, a polysiloxane antifoaming agent, and 1 g of polyethylene slip agent are added.
상기와 같이 만들어진 감광 잉크 조성물의 입도를 조절하고, 감광 캡슐이 서로 엉키는 것을 억제하기 위하여 감광 잉크 조성물이 3롤(Roll) 밀(Mill) 사이를 통과하게 하여 밀링(Milling) 공정을 수행하여 원하는 입도를 갖는 감광성 유성 잉크 조성물을 얻는다. 이때 조성물의 온도는 10∼35℃의 범위 내에서 밀링하고, 롤과 롤 사이의 압력을 조절하여 갭슐 입자가 깨지지 않도록 하여야 한다. In order to control the particle size of the photosensitive ink composition made as described above and to prevent the photosensitive capsule from tangling with each other, the photosensitive ink composition is passed through a three roll mill to perform a milling process to perform a desired particle size. A photosensitive oily ink composition having At this time, the temperature of the composition should be milled in the range of 10 to 35 ℃, and the pressure between the roll and the roll should be adjusted so as not to break the capsule particles.
이상, 본 발명의 바람직한 실시예를 들어 상세하게 설명하였으나, 본 발명은 상기 실시예에 한정되는 것은 아니며, 본 발명의 기술적 사상의 범위내에서 당 분야에서 통상의 지식을 가진 자에 의하여 여러 가지 변형이 가능하다.As mentioned above, although preferred embodiment of this invention was described in detail, this invention is not limited to the said embodiment, A various deformation | transformation by a person of ordinary skill in the art within the scope of the technical idea of this invention is carried out. This is possible.
Claims (11)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020090120929A KR101095444B1 (en) | 2009-12-08 | 2009-12-08 | Photosensitive ink composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020090120929A KR101095444B1 (en) | 2009-12-08 | 2009-12-08 | Photosensitive ink composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20110064367A true KR20110064367A (en) | 2011-06-15 |
| KR101095444B1 KR101095444B1 (en) | 2011-12-16 |
Family
ID=44397818
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020090120929A Active KR101095444B1 (en) | 2009-12-08 | 2009-12-08 | Photosensitive ink composition |
Country Status (1)
| Country | Link |
|---|---|
| KR (1) | KR101095444B1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9733132B2 (en) | 2011-09-30 | 2017-08-15 | Lg Hausys, Ltd. | In-mold transfer film which changes its color according to a temperature and which has a scent-emitting function and method for manufacturing same |
| CN119708907A (en) * | 2024-11-01 | 2025-03-28 | 东莞市鸿亿丝印器材有限公司 | Friction-resistant quick-drying odorless ink and preparation method thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003128975A (en) | 2001-10-29 | 2003-05-08 | Pilot Ink Co Ltd | Photochromic ink composition for marking pen and marking pen including the same |
| JP2005314659A (en) | 2004-03-29 | 2005-11-10 | Pilot Ink Co Ltd | Water-based photochromic ink composition for ballpoint pen and ballpoint pen comprising the same therein |
| JP4838915B2 (en) | 2005-10-21 | 2011-12-14 | パイロットインキ株式会社 | Photochromic material and liquid composition using the same |
| JP2007223253A (en) * | 2006-02-27 | 2007-09-06 | Pilot Ink Co Ltd | Color memory type discoloring writing instrument |
-
2009
- 2009-12-08 KR KR1020090120929A patent/KR101095444B1/en active Active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9733132B2 (en) | 2011-09-30 | 2017-08-15 | Lg Hausys, Ltd. | In-mold transfer film which changes its color according to a temperature and which has a scent-emitting function and method for manufacturing same |
| CN119708907A (en) * | 2024-11-01 | 2025-03-28 | 东莞市鸿亿丝印器材有限公司 | Friction-resistant quick-drying odorless ink and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| KR101095444B1 (en) | 2011-12-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TWI440645B (en) | Copolymer and its use | |
| TWI577743B (en) | Pigment composition, inkjet recording ink, coloring composition for color filter, and color filter | |
| JP5490159B2 (en) | Ink composition, image forming method, and printed matter using the same | |
| CN101652448B (en) | TTI indicator with balanced photochemical processes | |
| EP2195395B1 (en) | New organic fluorescent sulfonyl ureido benzoxazinone pigments | |
| TW200811246A (en) | Azo dye, heat-sensitive transfer recording ink sheet, heat-sensitive transfer recording method, color toner, inkjet ink and color filter | |
| JPH0931453A (en) | Microcapsule and element using the same | |
| CN109648956A (en) | Photochromic material and preparation method thereof, application | |
| KR101095444B1 (en) | Photosensitive ink composition | |
| CN107743509B (en) | Use of novel naphthol AS pigment mixtures in printing materials | |
| US6613140B2 (en) | Azo orange pigment composition | |
| JP6196370B2 (en) | Near-infrared reflective / transmissive azo pigments, methods for producing near-infrared reflective / transmissive azo pigments, colorant compositions using these azo pigments, article coloring methods and colored articles | |
| JP4787510B2 (en) | Fluorescent coloring composition, coloring method and colored article | |
| JP3833563B2 (en) | Thermosensitive color-changing composition with excellent light fastness | |
| US10508201B2 (en) | Methods for manufacturing azoic pigments | |
| JP2006022202A (en) | Photochromic liquid composition | |
| JP2014177575A (en) | Method for preparing monoazo pigment composition, toner, and inkjet ink | |
| JP3647107B2 (en) | Ink for inkjet printer and printed matter using the same | |
| CN107667148A (en) | Novel naphthol as pigments | |
| JP5164365B2 (en) | Photochromic microcapsule | |
| JP7221824B2 (en) | Ink composition for water-based ballpoint pen | |
| TW201139565A (en) | Process for producing azo compounds, pigment dispersion, coloring composition, ink for inkjet recording, coloring composition for color filter, and color filter | |
| JP7109943B2 (en) | PIGMENT DISPERSION, TONER MANUFACTURING METHOD, WATER-BASED INK AND TRIAZO COMPOUND | |
| TWI612102B (en) | Method for producing near-infrared reflection or penetrating azo pigment, near-infrared reflection or penetrating azo pigment, coloring agent composition using the same, pigment coloring method and coloring article | |
| JP2006089577A (en) | Ink composition and recording method using the ink composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A201 | Request for examination | ||
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20091208 |
|
| PA0201 | Request for examination | ||
| PG1501 | Laying open of application | ||
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20110920 Patent event code: PE09021S01D |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20111123 Patent event code: PE09021S01D |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20111130 |
|
| GRNT | Written decision to grant | ||
| PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20111212 Patent event code: PR07011E01D |
|
| PR1002 | Payment of registration fee |
Payment date: 20111212 End annual number: 3 Start annual number: 1 |
|
| PG1601 | Publication of registration | ||
| FPAY | Annual fee payment |
Payment date: 20140922 Year of fee payment: 4 |
|
| PR1001 | Payment of annual fee |
Payment date: 20140922 Start annual number: 4 End annual number: 4 |
|
| FPAY | Annual fee payment |
Payment date: 20150921 Year of fee payment: 5 |
|
| PR1001 | Payment of annual fee |
Payment date: 20150921 Start annual number: 5 End annual number: 5 |
|
| FPAY | Annual fee payment |
Payment date: 20160926 Year of fee payment: 6 |
|
| PR1001 | Payment of annual fee |
Payment date: 20160926 Start annual number: 6 End annual number: 6 |
|
| FPAY | Annual fee payment |
Payment date: 20170925 Year of fee payment: 7 |
|
| PR1001 | Payment of annual fee |
Payment date: 20170925 Start annual number: 7 End annual number: 7 |
|
| FPAY | Annual fee payment |
Payment date: 20181001 Year of fee payment: 8 |
|
| PR1001 | Payment of annual fee |
Payment date: 20181001 Start annual number: 8 End annual number: 8 |
|
| FPAY | Annual fee payment |
Payment date: 20190923 Year of fee payment: 9 |
|
| PR1001 | Payment of annual fee |
Payment date: 20190923 Start annual number: 9 End annual number: 9 |
|
| PR1001 | Payment of annual fee |
Payment date: 20200923 Start annual number: 10 End annual number: 10 |
|
| PR1001 | Payment of annual fee |
Payment date: 20210929 Start annual number: 11 End annual number: 11 |
|
| PR1001 | Payment of annual fee |
Payment date: 20230524 Start annual number: 12 End annual number: 12 |
|
| PR1001 | Payment of annual fee |
Payment date: 20231108 Start annual number: 13 End annual number: 13 |
|
| PR1001 | Payment of annual fee |
Payment date: 20241209 Start annual number: 14 End annual number: 14 |