JPH08290683A - Heat-sensitive transfer recording method - Google Patents
Heat-sensitive transfer recording methodInfo
- Publication number
- JPH08290683A JPH08290683A JP7100915A JP10091595A JPH08290683A JP H08290683 A JPH08290683 A JP H08290683A JP 7100915 A JP7100915 A JP 7100915A JP 10091595 A JP10091595 A JP 10091595A JP H08290683 A JPH08290683 A JP H08290683A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- image
- sensitive transfer
- sensitive
- ink layer
- 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.)
- Pending
Links
- 238000012546 transfer Methods 0.000 title claims abstract description 82
- 238000000034 method Methods 0.000 title claims abstract description 40
- 238000007639 printing Methods 0.000 claims abstract description 40
- 239000000049 pigment Substances 0.000 claims abstract description 31
- 239000000463 material Substances 0.000 claims abstract description 27
- 239000002245 particle Substances 0.000 claims abstract description 6
- 239000010410 layer Substances 0.000 claims description 47
- 239000012790 adhesive layer Substances 0.000 claims description 11
- 229920000620 organic polymer Polymers 0.000 claims description 6
- 230000003287 optical effect Effects 0.000 claims description 5
- 238000003825 pressing Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 abstract description 4
- 229920000642 polymer Polymers 0.000 abstract description 3
- -1 acrylic acid Dienes Chemical class 0.000 description 25
- 238000000576 coating method Methods 0.000 description 18
- 239000011248 coating agent Substances 0.000 description 17
- 238000000859 sublimation Methods 0.000 description 16
- 230000008022 sublimation Effects 0.000 description 16
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 239000010408 film Substances 0.000 description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 229920001577 copolymer Polymers 0.000 description 11
- 229920000728 polyester Polymers 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 230000004927 fusion Effects 0.000 description 6
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 125000006162 fluoroaliphatic group Chemical group 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- 239000011976 maleic acid Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229920006267 polyester film Polymers 0.000 description 4
- 239000002491 polymer binding agent Substances 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
- 239000001993 wax Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-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
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 229940124530 sulfonamide Drugs 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 2
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-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
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 2
- XUDBVJCTLZTSDC-UHFFFAOYSA-N 2-ethenylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C=C XUDBVJCTLZTSDC-UHFFFAOYSA-N 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- UWRZIZXBOLBCON-UHFFFAOYSA-N 2-phenylethenamine Chemical compound NC=CC1=CC=CC=C1 UWRZIZXBOLBCON-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-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
- 239000004698 Polyethylene Substances 0.000 description 2
- 229920002873 Polyethylenimine Polymers 0.000 description 2
- 235000006040 Prunus persica var persica Nutrition 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- 235000010724 Wisteria floribunda Nutrition 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 235000013985 cinnamic acid Nutrition 0.000 description 2
- 229930016911 cinnamic acid Natural products 0.000 description 2
- 235000019383 crystalline wax Nutrition 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 150000002689 maleic acids Chemical class 0.000 description 2
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 2
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 2
- DNPFOADIPJWGQH-UHFFFAOYSA-N octan-3-yl prop-2-enoate Chemical compound CCCCCC(CC)OC(=O)C=C DNPFOADIPJWGQH-UHFFFAOYSA-N 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- XESUCHPMWXMNRV-UHFFFAOYSA-M sodium;2-ethenylbenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC=C1C=C XESUCHPMWXMNRV-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 150000003456 sulfonamides Chemical class 0.000 description 2
- 238000007651 thermal printing Methods 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- OZSKVMIBRHDIET-UHFFFAOYSA-N 12-hydroxy-n-(2-hydroxyethyl)octadecanamide Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)NCCO OZSKVMIBRHDIET-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- 244000144730 Amygdalus persica Species 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- 239000004169 Hydrogenated Poly-1-Decene Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 240000005809 Prunus persica Species 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 206010057040 Temperature intolerance Diseases 0.000 description 1
- 229920000690 Tyvek Polymers 0.000 description 1
- 239000004775 Tyvek Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229920006125 amorphous polymer Polymers 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 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 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000008543 heat sensitivity Effects 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- CFKPIIMZDNLAQL-UHFFFAOYSA-N methyl acetate;toluene Chemical compound COC(C)=O.CC1=CC=CC=C1 CFKPIIMZDNLAQL-UHFFFAOYSA-N 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 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 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 230000008542 thermal sensitivity Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical class C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明はサーマルヘッドプリンタ
ーやレーザー光を利用して、顔料を含有する感熱インキ
層を受像シート上に熱転写し、面積階調のみで高品質の
多階調カラー画像などを形成する方法に関し、更には、
その受像シート材料上に形成した画像を印刷本紙上に転
写して印刷用プルーフを形成する方法に関する。更に詳
しくは、一種類の受像シートを用いて、その受像シート
上に画像を形成させて迅速に画像が確認でき、必要に応
じて、その受像シート上の画像を印刷本紙上に転写する
事により更に正確に印刷の仕上がり具合を判定できる方
法に関する。更には、印刷分野におけるカラープルーフ
に止まらず、カードや屋外ディスプレー、メーターディ
スプレー、一般のカラーコピーへの応用が可能な感熱転
写記録方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention uses a thermal head printer or laser light to thermally transfer a heat-sensitive ink layer containing a pigment onto an image-receiving sheet to obtain a high-quality multi-tone color image with only area gradation. And a method of forming
The present invention relates to a method of forming a printing proof by transferring an image formed on the image receiving sheet material onto a printing actual paper. More specifically, by using one type of image-receiving sheet, an image can be formed on the image-receiving sheet and the image can be confirmed quickly, and by transferring the image on the image-receiving sheet onto the printing original paper, if necessary. The present invention also relates to a method that can more accurately determine the finish of printing. Furthermore, the present invention relates to a thermal transfer recording method which is applicable not only to color proof in the printing field but also to cards, outdoor displays, meter displays and general color copying.
【0002】[0002]
【従来の技術】従来、サーマルヘッドプリンターやレー
ザー光を使用し、カラー画像を形成する感熱転写記録方
式としては、昇華型染料転写方式と熱溶融型転写方式が
知られている。昇華型染料転写方式は、昇華型染料と結
合剤とからなる転写層を支持体上に設けた転写シートを
受像シートと重ね、転写シートの支持体の裏側からサー
マルヘッドにより画像様に熱を与え、昇華型染料を昇華
させて受像シートに転写し、受像シート上に画像を形成
する方式である。イエロー,マゼンタ,シアンよりなる
転写シートを使用することによりカラー画像を形成する
ことも出来る。2. Description of the Related Art Conventionally, as a thermal transfer recording system for forming a color image by using a thermal head printer or a laser beam, a sublimation dye transfer system and a thermal fusion transfer system are known. In the sublimation dye transfer method, a transfer sheet having a transfer layer consisting of a sublimation dye and a binder provided on a support is superposed on an image receiving sheet, and heat is applied imagewise by a thermal head from the back side of the transfer sheet support. , A sublimation dye is sublimated and transferred to an image receiving sheet to form an image on the image receiving sheet. It is also possible to form a color image by using a transfer sheet composed of yellow, magenta and cyan.
【0003】しかしながら、昇華型染料方式は以下の欠
点を有している。 1.画像の階調表現が主として濃度階調(染料の種か量
を制御)を利用するものであり、写真に類似する階調を
好む民生用の一部の目的には適しているが、例えば面積
階調のみで階調表現をしている印刷分野で使用されてい
るカラープルーフ用等には適していない。 2.画像形成が染料の昇華を利用しているため、出来上
がり画像のエッジシャープネスが不満足であり、又太線
に比べ細線のベタ濃度が薄くなる。これらは文字画像の
品質に関して重大な欠点となる。 3.画像の耐久性が劣るので、耐熱性や耐光性を要求す
る分野への展開が限定されている。 4.感熱記録感度が熱溶融型転写方式に比べ低いため、
将来期待されている高解像力サーマルヘッドを用いる高
速記録材料としては適していない。 5.熱溶融型転写材料に比べ感材が高価である。 6.専用の受像シートが必要であり、印刷で用いられて
いる本紙上に画像形成する事ができない。この為、本紙
に印刷したときに本紙の微妙な色合いや風合いが画像に
与える影響を見ることが出来ず、印刷用プルーフとして
は適していない。However, the sublimation dye method has the following drawbacks. 1. The gradation representation of an image mainly uses density gradation (controls the kind or amount of dye) and is suitable for some purposes for consumer who prefer gradation similar to photographs, but It is not suitable for color proof, which is used in the printing field where gradation is expressed only by gradation. 2. Since the image formation uses dye sublimation, the edge sharpness of the finished image is unsatisfactory, and the solid density of thin lines is lighter than that of thick lines. These are serious drawbacks regarding the quality of character images. 3. Since the durability of images is inferior, development in fields requiring heat resistance and light resistance is limited. 4. Since the thermal recording sensitivity is lower than that of the thermal fusion transfer method,
It is not suitable as a high-speed recording material using a high resolution thermal head, which is expected in the future. 5. The sensitive material is more expensive than the heat-melt transfer material. 6. A dedicated image receiving sheet is required, and images cannot be formed on the actual paper used for printing. For this reason, it is not suitable as a proof for printing because it is not possible to see the effect of the delicate color and texture of the paper on the image when printed on the paper.
【0004】一方、熱溶融型転写方式は支持体上に顔料
や染料などの色材とワックスなどの結合剤からなる熱溶
融性の転写層を設けた転写シートを受像シートと重ね、
転写シートの支持体の裏側からサーマルヘッドにより画
像様に熱を与え、転写層を溶融して受像シート像に融着
させて画像を形成させる方式である。熱溶融型転写方式
は昇華型染料転写方式に比べて、1.感熱感度が高い,
2.材料が安価である,3.画像の耐光性が優れてい
る、4.普通紙に転写可能である。等の利点を有してい
るものの、下記の欠点を有している。熱溶融転写方式の
最大の欠点の1つは、昇華型染料転写方式に比べカラー
画像の品質が劣ることに有る。これは、この方式が本来
濃度階調による階調再現ではなく、2値記録であること
による。勿論、この2値記録性を改善し、熱溶融転写方
式において、多階調のカラー画像を形成することを目的
に濃度階調を達成するためのインキ転写層の提案が種々
なれてきた。しかしながら、これらの考え方の基本は、
サーマルヘッドによる加熱でインキ層の結合剤が溶融し
て粘度が低下する結果受像シートへの粘着力が増加して
転写する特性を利用し、サーマルヘッドの昇温を制御し
てインキ層内部の凝集破壊を制御し、熱転写記録のガン
マ特性を軟調化することに有る。それ故、熱溶融転写方
式は昇華染料転写方式に比べ、多階調性の点において劣
ることになる。また一般に細線などの画像濃度の再現性
も劣る問題点を生じることになる。特に、普通紙に記録
できる利点はあるものの、平滑な普通紙でも上記の画質
に関する欠点を有しており、まして、印刷に使用される
様々な紙上に高画質の印画を行うことは難しい。On the other hand, in the heat-melt transfer method, a transfer sheet having a heat-melt transfer layer made of a coloring material such as pigment or dye and a binder such as wax is provided on a support, is superposed on an image receiving sheet,
This is a method in which heat is applied imagewise from the back side of the support of the transfer sheet by a thermal head to melt the transfer layer and fuse it to the image of the image-receiving sheet to form an image. Compared to the sublimation dye transfer method, the heat-melt transfer method has 1. High heat sensitivity,
2. The material is inexpensive, 3. 3. The image has excellent light resistance. It can be transferred to plain paper. However, it has the following drawbacks. One of the biggest drawbacks of the thermal fusion transfer system is that the quality of the color image is inferior to that of the sublimation dye transfer system. This is because this method is not binary reproduction by density gradation, but binary recording. Needless to say, various proposals have been made for an ink transfer layer for improving the binary recording property and achieving density gradation for the purpose of forming a multi-gradation color image in the thermal fusion transfer method. However, the basis of these ideas is
As the thermal head heats the binder in the ink layer to lower the viscosity, the adhesive strength to the image receiving sheet increases and transfer is performed, and the temperature rise of the thermal head is controlled to agglomerate inside the ink layer. It is intended to control destruction and soften the gamma characteristic of thermal transfer recording. Therefore, the thermal fusion transfer method is inferior in terms of multi-gradation to the sublimation dye transfer method. Further, in general, the reproducibility of the image density of fine lines and the like will be inferior. In particular, although there is an advantage of being able to record on plain paper, even plain plain paper has the above-mentioned drawbacks regarding image quality, and it is difficult to perform high-quality printing on various papers used for printing.
【0005】また熱溶融型転写方式は、通常低融点の結
晶性ワックスをインキ層の結合剤として用いているた
め、記録体中の熱印字の際のニジミにより、解像力の低
下あるいは転写定着画像の強度が弱いなどの問題点を有
している。更には、結晶性ワックス類は結晶相の光散乱
により透明な画像を得難いという欠点を有している。こ
のことはイエロー,マゼンタ,シアンなどの重なりとし
てのカラー画像を形成する場合には大きな欠点となる。
更に透明性を劣化させる要因としては、インキ層総量に
対する顔料比率にも関係が有り、特公昭63−6502
9号明細書に述べられているごとく、通常着色剤はイン
キ層の総量に対して20重量部以下で用いられ、これ以
上で使用される場合は透明性が低下する。In the heat-melt transfer method, since a crystalline wax having a low melting point is usually used as a binder for the ink layer, the resolution may be lowered or the transfer-fixed image may not be formed due to blurring during thermal printing on the recording material. It has problems such as weak strength. Furthermore, the crystalline waxes have the drawback that it is difficult to obtain a transparent image due to the light scattering of the crystalline phase. This is a big drawback when forming color images as overlapping of yellow, magenta, cyan, and the like.
Further, as a factor that deteriorates the transparency, there is also a relation with the pigment ratio with respect to the total amount of the ink layer.
As described in Japanese Patent No. 9, the colorant is usually used in an amount of 20 parts by weight or less based on the total amount of the ink layer, and when it is used in an amount larger than this, the transparency is lowered.
【0006】熱溶融転写方式のカラー画像の色再現を改
良するために、種々の提案がなされてきた。例えば特開
昭61−244592(特公平5−13072)号明細
書中には、連続階調性を持続した上で透明性,定着画像
強度等を改良する目的で、少なくとも50重量%以上の
非晶質ポリマーと離型性物質と着色剤(染料や顔料)よ
りなる感熱インキ層の提案がなされている。該公報にお
いては、先ず透明性に関しては、非晶質ポリマーが50
重量%以下では,感熱インキ材料の透明性が著しく悪化
し良好なカラー再現性が得られない。特に良好な透明性
を示すには、70重量%が必要であると述べられてい
る。また感熱インキ層の膜厚に関しては0.5μm〜5
0μm、通常は1μmから20μmが好ましいと述べら
れている。 しかしながら、特にプルーフ用途などの点
から、画像形成に関してはシアン,マゼンタ,イエロー
は反射濃度が1.4前後必要であり、特にブラックに関
しては1.7前後必要であるにもかかわらず該明細書中
には1μm以下の顔料径インキ層膜厚で透明性を維持し
た上で,どれだけの濃度が得られるかの記載は全くな
い。更に実施例においても通常のワックス系とほとんど
同じくインキ層の膜厚は3μm前後である。すなわち該
明細書においては、インキ層の透明性を維持した上で、
1.0μm以下の膜厚で光学的反射濃度を1.0以上に
するための技術的開示は何等なされていない。又、様々
な紙上に高画質の画像を形成する技術の開示は何等なさ
れていない。Various proposals have been made in order to improve the color reproduction of a heat-melt transfer type color image. For example, in Japanese Patent Application Laid-Open No. 61-244592 (Japanese Patent Publication No. 5-13072), in order to improve the transparency, the strength of a fixed image and the like while maintaining continuous gradation, at least 50 wt. A thermal ink layer composed of a crystalline polymer, a releasing material and a coloring agent (dye or pigment) has been proposed. In this publication, firstly, regarding the transparency, the amorphous polymer is 50
When the content is less than 10% by weight, the transparency of the thermal ink material is significantly deteriorated and good color reproducibility cannot be obtained. It is stated that 70% by weight is necessary to show particularly good transparency. The thickness of the thermal ink layer is 0.5 μm to 5 μm.
It is stated that 0 μm, usually 1 μm to 20 μm is preferred. However, from the viewpoint of proof use, cyan, magenta, and yellow require a reflection density of about 1.4 for image formation, and about 1.7 for black, in spite of the fact that they are required in the specification. Does not describe how much density can be obtained while maintaining transparency at an ink layer thickness of pigment diameter of 1 μm or less. Further, also in the examples, the film thickness of the ink layer is about 3 μm, which is almost the same as the usual wax type. That is, in the specification, after maintaining the transparency of the ink layer,
No technical disclosure is made for making the optical reflection density 1.0 or more at a film thickness of 1.0 μm or less. Further, there is no disclosure of a technique for forming a high quality image on various papers.
【0007】一方、サーマルヘッドプリンターの技術的
進歩は著しい。サーマルヘッドそのものの高解像力化の
みならず面積階調のみで多階調記録を可能にする印字方
式としては、特開平4−19163,特開平5−155
057号明細書に記載の副走査分割方式や、「電子写真
学会年次大会1992/7/6予稿集」に記載の熱集中型方式な
どが提案されている。On the other hand, the technical progress of thermal head printers is remarkable. As a printing method which enables multi-gradation recording only with area gradation as well as high resolution of the thermal head itself, JP-A-4-19163, JP-A-5-155
The sub-scanning division method described in the specification No. 057 and the heat concentration type method described in "Annual Meeting of the Electrophotographic Society 1992/7/6 Proceedings" have been proposed.
【0008】[0008]
【発明が解決しようとする課題】感熱転写方式を用いて
印刷用プルーフを作成する場合、以下の問題を解決する
必要がある。 1. 転写インキ層の透明性を維持した上で、各色とも
所定の画像濃度があること。 2. 印刷本誌に転写した画像が、質感、画像の光沢度
等印刷物近似性に優れること。 3. 画像の出来上がり状態を迅速に判断できること。When making a printing proof using a thermal transfer method, it is necessary to solve the following problems. 1. While maintaining the transparency of the transfer ink layer, each color should have a predetermined image density. 2. Printing Images transferred to this magazine should have good approximation of printed matter such as texture and image gloss. 3. To be able to quickly determine the finished state of an image.
【0009】しかしながら、上述の通り、従来の熱溶融
転写方式を用いる限りでは、印刷本紙上への画像形成は
困難であり、また、転写インキ層の透明性を維持して所
定の画像濃度を達成し、高画質の画像を得ることは困難
である。一方、印刷本紙上に画像形成を行う従来の種々
の方法では、画像形成処理に時間がかかり、画像の出来
上がり状態を迅速に判断するとができない。本発明の目
的はまさにこの解決手段を提案することにある。However, as described above, it is difficult to form an image on the actual printing paper as long as the conventional thermal fusion transfer method is used, and the transparency of the transfer ink layer is maintained to achieve a predetermined image density. However, it is difficult to obtain a high quality image. On the other hand, in the various conventional methods of forming an image on the actual printing paper, the image forming process takes time, and it is not possible to quickly determine the finished state of the image. The aim of the invention is to propose exactly this solution.
【0010】[0010]
【課題を解決するための手段】本発明者等は鋭意研究を
重ねた結果、従来の昇華染料感熱転写方式や溶融転写方
式では実現出来なかった、印刷用プルーフに適した、高
画質の画像を迅速に得る事ができ、更に、必要に応じて
印刷本紙上に画像が形成でき印刷本紙に由来する微妙な
色調や紙質感も判断できる感熱転写記録の方法を見いだ
した。また、通常は印刷本紙上に画像を形成させるため
に必要な加熱あるいは加圧転写の時間と手間を省いて画
像の出来上がり状態を迅速に判断でき、必要に応じて必
要な画像を印刷本紙に転写することができる方法を見い
だした。Means for Solving the Problems As a result of intensive studies by the present inventors, a high-quality image suitable for a printing proof, which could not be realized by a conventional sublimation dye thermal transfer method or melt transfer method, was obtained. We have found a method of thermal transfer recording that can be quickly obtained, and that an image can be formed on the actual printing paper as needed, and the subtle color tone and paper texture derived from the actual printing paper can be judged. In addition, it is possible to quickly judge the finished state of the image by omitting the time and labor of heating or pressure transfer normally required to form the image on the printing main sheet, and transfer the required image to the printing main sheet as necessary. I've found a way to do it.
【0011】即ち、本発明の目的は、白色支持体上に熱
接着層を有する受像シートを用い、30〜70重量部の
顔料と25〜60重量部の軟化点が40℃〜150℃の
有機高分子重合体を含み、膜厚が0.2μm〜1.0μ
mの範囲に有る感熱インキ層を有し、該感熱インキ層中
の顔料の70%以上の粒径が1.0μm以下であり、か
つ転写画像の光学反射濃度が白色支持体上で1.0以上
有る感熱転写記録材料の裏面から熱ヘッドにて該受像シ
ートにインキ層を感熱転写し感熱転写画像を形成させる
第一の方法と、該受像シートに形成された該感熱転写画
像を印刷本紙と重ね合わせ少なくとも加圧し、必要に応
じて加熱することにより該感熱転写画像を印刷本紙上に
転写し画像を形成する第二の方法の何れかを選択する事
を特徴とする感熱転写記録方法により達成された。That is, an object of the present invention is to use an image-receiving sheet having a heat-adhesive layer on a white support and to use 30 to 70 parts by weight of a pigment and 25 to 60 parts by weight of an organic compound having a softening point of 40 to 150 ° C. Including high-molecular polymer, film thickness 0.2μm ~ 1.0μ
m has a heat-sensitive ink layer, 70% or more of the pigments in the heat-sensitive ink layer have a particle size of 1.0 μm or less, and the transferred image has an optical reflection density of 1.0 on a white support. A first method of forming a heat-sensitive transfer image by heat-transferring an ink layer from the back surface of the heat-sensitive transfer recording material to the image-receiving sheet with a thermal head, and printing the heat-sensitive transfer image formed on the image-receiving sheet as a main sheet. Achieved by a heat-sensitive transfer recording method characterized by selecting at least one of the second method of forming an image by transferring the heat-sensitive transfer image onto a printing actual paper by superposing at least pressure and heating if necessary. Was done.
【0012】以下、本発明を詳細に説明する。本発明の
感熱転写記録材料のインキ層に含まれる顔料としては、
種々の公知の顔料が使用でき、例えばカーボンブラッ
ク,アゾ系,フタロシアニン系,キナクリドン系,チオ
インジゴ系,アンスラキノン系,イソインドリノン系等
の顔料が挙げられる。これらは2種類以上組み合わせて
使用することも可能であり、また色相調整のため公知の
染料を添加してもよい。The present invention will be described in detail below. The pigment contained in the ink layer of the heat-sensitive transfer recording material of the present invention,
Various known pigments can be used, and examples thereof include carbon black, azo pigments, phthalocyanine pigments, quinacridone pigments, thioindigo pigments, anthraquinone pigments and isoindolinone pigments. These may be used in combination of two or more, and a known dye may be added for adjusting the hue.
【0013】本発明の感熱転写記録材料のインキ層に含
まれる軟化点が40℃〜150℃の非晶質有機高分子結
合体としては、例えばブチラール樹脂,ポリアミド樹
脂,ポリエチレンイミン樹脂,スルホンアミド樹脂,ポ
リエステルポリオール樹脂,石油樹脂,スチレン,αー
メチルスチレン,2ーメチルスチレン,クロルスチレ
ン,ビニル安息香酸,ビニルベンゼンスルホン酸ソー
ダ,アミノスチレン等のスチレン及びその誘導体,置換
体の単独重合体や共重合体,メチルメタクリレート,エ
チルメタクリレート,ヒドロキシエチルメタクリレート
等のメタクリル酸エステル類及びメタクリル酸,メチル
アクリレート,エチルアクリレート,ブチルアクリレー
ト,αーエチルヘキシルアクリレート等のアクリル酸エ
ステル及びアクリル酸,ブタジエン,イソジエン,イソ
プレン等のジエン類,アクリロニトリル,ビニルエーテ
ル類,マレイン酸及びマレイン酸エステル類,無水マレ
イン酸,ケイ皮酸,塩化ビニル,酢酸ビニル等のビニル
系単量体の単独あるいは他の単量体等の共重合体を用い
ることができる。これらの樹脂は2種以上混合して用い
ることもできる。Examples of the amorphous organic polymer binder having a softening point of 40 ° C. to 150 ° C. contained in the ink layer of the thermal transfer recording material of the present invention include butyral resin, polyamide resin, polyethyleneimine resin, sulfonamide resin. , Polyester polyol resin, petroleum resin, styrene, α-methylstyrene, 2-methylstyrene, chlorostyrene, vinylbenzoic acid, sodium vinylbenzene sulfonate, styrene and its derivatives such as aminostyrene, homopolymers and copolymers of substitution products, methyl Methacrylic acid esters such as methacrylate, ethyl methacrylate, hydroxyethyl methacrylate, and acrylic acid esters such as methacrylic acid, methyl acrylate, ethyl acrylate, butyl acrylate, α-ethylhexyl acrylate, and acrylic acid Dienes such as tadiene, isodiene and isoprene, acrylonitrile, vinyl ethers, maleic acid and maleic acid esters, maleic anhydride, cinnamic acid, vinyl chloride, vinyl acetate and other vinyl monomers, alone or in other amounts A copolymer such as a body can be used. Two or more kinds of these resins may be mixed and used.
【0014】これらのうち、ブチラール樹脂やスチレン
/マレイン酸ハーフエステル樹脂等が好ましい。これら
樹脂の軟化点は40℃〜150℃の範囲で選ばれるべき
である。150℃を越えると熱記録感度が低く、他方4
0℃未満ではインキ層の耐接着性が劣る。Of these, butyral resin and styrene / maleic acid half ester resin are preferred. The softening point of these resins should be selected in the range of 40 ° C to 150 ° C. If the temperature exceeds 150 ° C, the thermal recording sensitivity will be low, while the other 4
If the temperature is lower than 0 ° C, the ink layer has poor adhesion resistance.
【0015】これらインキ層には、熱印字の際のインキ
層の支持体からの離型性及び熱感度向上の観点から種々
の離型剤や軟化剤をインキ層総量に対して1重量%から
20重量%の範囲で加えることも可能である。具体的に
は、例えばパルミチン酸,ステアリン酸等の高級脂肪
酸,ステアリン酸亜鉛の如き脂肪酸金属塩類,脂肪酸エ
ステル類もしくはその部分ケン化物,脂肪酸アミド類等
の脂肪酸誘導体,高級アルコール類,多価アルコール類
のエテル等誘導体,パラフィンワックス,カルナバワッ
クス,モンタンワックス,ミツロウ,木ロウ,キャンデ
リラワックス等のワックス類,粘度平均分子量が約1,
000から10,000程度の低分子量ポリエチレン,
ポリプロピレン,ポリブチレン等のポリオレフイン類,
或いはオレフイン,αーオレフイン類と無水マレイン
酸,アクリル酸,メタクリル酸等の有機酸,酢酸ビニル
等との低分子量共重合体,低分子量酸化ポリオレフイ
ン,ハロゲン化ポリオレフイン類,ラウリルメタクリレ
ート,ステアリルメタクリレート等長鎖アルキル側鎖を
有するメタクリル酸エステル,メタクリル酸エステル類
の単独もしくはスチレン類等のビニル系単量体との共重
合体、ポリジメチルシロキサン,ポリジフェニルシロキ
サン等の低分子量シリコーンレジン及びシリコーン変性
有機物質等が挙げられ、1種あるいは2種以上選択して
用いることができる。From the viewpoint of improving the releasability of the ink layer from the support and the thermal sensitivity at the time of thermal printing, various releasing agents and softening agents are added to these ink layers in an amount of from 1% by weight to the total amount of the ink layer. It is also possible to add in the range of 20% by weight. Specifically, for example, higher fatty acids such as palmitic acid and stearic acid, fatty acid metal salts such as zinc stearate, fatty acid esters or partial saponification products thereof, fatty acid derivatives such as fatty acid amides, higher alcohols, and polyhydric alcohols. Waxes such as ether derivatives, paraffin wax, carnauba wax, montan wax, beeswax, wood wax, candelilla wax, etc., viscosity average molecular weight of about 1,
000 to 10,000 low molecular weight polyethylene,
Polyolefins such as polypropylene and polybutylene,
Or low molecular weight copolymers of olefins, α-olefins and organic acids such as maleic anhydride, acrylic acid, methacrylic acid, etc., low molecular weight copolymers, low molecular weight oxidized polyolefins, halogenated polyolefins, lauryl methacrylate, stearyl methacrylate, etc. Methacrylic acid ester having alkyl side chain, copolymer of methacrylic acid ester alone or copolymer with vinyl monomer such as styrene, low molecular weight silicone resin such as polydimethylsiloxane and polydiphenylsiloxane, and silicone modified organic substance And one or more of them can be selected and used.
【0016】これら感熱インキ層の光学濃度は、先に述
べた理由により白色支持体上に転写した際にその反射濃
度が1.0以上なければならない。また膜厚は0.2μ
mから1.0μmの範囲が好ましい。1.0μmよりも
大きな厚いインキ層においては、面積階調再現性におい
てシャドウ部がつぶれやすかったり、ハイライト部がと
びやすっかたりして、結果的に階調再現性が劣ることな
る。一方、0.2μmより下の膜厚では,所定の濃度を
出すことが難しい。The optical densities of these thermal ink layers must have a reflection density of 1.0 or more when transferred onto a white support for the reasons described above. The film thickness is 0.2μ
The range of m to 1.0 μm is preferable. In the case of a thick ink layer having a thickness of more than 1.0 μm, in the area gradation reproducibility, the shadow part is easily crushed and the highlight part is easily skipped, resulting in poor gradation reproducibility. On the other hand, if the film thickness is less than 0.2 μm, it is difficult to obtain a predetermined concentration.
【0017】これらの薄膜で所定の濃度を出すために
は、該インキ層中の顔料が30重量部から70重量部,
非晶質有機高分子結合体が25重量〜60重量部で、必
要に応じ添加される離型性物質や軟膜剤の総量が1重量
部から15重量部であることが好ましい。顔料比率がこ
れ以下では上記所定の膜厚で濃度を出すことが難しい。
また顔料の粒径は、顔料の70%以上が1.0μm以下
であることが必要である。粒径が大きい場合にはカラー
再現性時の各色の重なり部の透明性が損なわれ、かつ先
の膜厚と濃度の関係の両者を満たすことが困難になる。In order to obtain a predetermined concentration with these thin films, the pigment in the ink layer is 30 to 70 parts by weight,
It is preferable that the amount of the amorphous organic polymer conjugate is 25 to 60 parts by weight, and the total amount of the releasing agent and the film softener added as necessary is 1 to 15 parts by weight. If the pigment ratio is less than this, it is difficult to obtain the density with the above-mentioned predetermined film thickness.
Further, regarding the particle size of the pigment, 70% or more of the pigment needs to be 1.0 μm or less. When the particle size is large, the transparency of the overlapping portions of the respective colors during color reproducibility is impaired, and it becomes difficult to satisfy both the relationship between the film thickness and the density.
【0018】これら顔料の非晶質有機高分子結合体への
分散に関しては、適切な溶剤を加えてボールミル、ダイ
ノミルをはじめとする、塗料分野で使用される種々の分
散方法が適用される。Regarding the dispersion of these pigments in the amorphous organic polymer binder, various dispersion methods used in the field of coating, such as ball mill and dyno mill, can be applied by adding an appropriate solvent.
【0019】本発明の熱接着層は主成分が有機高分子結
合体であり、有機高分子結合体としては、例えばブチラ
ール樹脂,ポリアミド樹脂,ポリエチレンイミン樹脂,
スルホンアミド樹脂,ポリエステルポリオール樹脂,石
油樹脂,スチレン,αーメチルスチレン,2ーメチルス
チレン,クロルスチレン,ビニル安息香酸,ビニルベン
ゼンスルホン酸ソーダ,アミノスチレン等のスチレン及
びその誘導体,置換体の単独重合体や共重合体,メチル
メタクリレート,エチルメタクリレート,ヒドロキシエ
チルメタクリレート等のメタクリル酸エステル類及びメ
タクリル酸,メチルアクリレート,エチルアクリレー
ト,ブチルアクリレート,αーエチルヘキシルアクリレ
ート等のアクリル酸エステル及びアクリル酸,ブタジエ
ン,イソジエン,イソプレン等のジエン類,アクリロニ
トリル,ビニルエーテル類,マレイン酸及びマレイン酸
エステル類,無水マレイン酸,ケイ皮酸,塩化ビニル,
酢酸ビニル等のビニル系単量体の単独あるいは他の単量
体等の共重合体を用いることができる。これらの樹脂は
2種以上混合して用いることもできる。The heat-adhesive layer of the present invention has an organic polymer binder as a main component, and examples of the organic polymer binder include butyral resin, polyamide resin, polyethyleneimine resin,
Sulfonamide resin, polyester polyol resin, petroleum resin, styrene, α-methylstyrene, 2-methylstyrene, chlorostyrene, vinyl benzoic acid, sodium vinylbenzene sulfonate, aminostyrene and other styrenes and their derivatives, homopolymers and copolymers of substitution products Methacrylates such as coalesce, methylmethacrylate, ethylmethacrylate, hydroxyethylmethacrylate and acrylates such as methacrylic acid, methylacrylate, ethylacrylate, butylacrylate, α-ethylhexylacrylate and acrylic acid, butadiene, isodiene, isoprene, etc. Dienes, acrylonitrile, vinyl ethers, maleic acid and maleic acid esters, maleic anhydride, cinnamic acid, vinyl chloride,
A vinyl monomer such as vinyl acetate may be used alone, or a copolymer of other monomers may be used. Two or more kinds of these resins may be mixed and used.
【0020】これらのうち、ブチラール樹脂やスチレン
/マレイン酸ハーフエステル樹脂等が好ましい。これら
樹脂の軟化点は40℃〜150℃の範囲で選ばれるべき
である。150℃を越えると熱記録感度が低く、他方4
0℃未満では耐接着性が劣る。Of these, butyral resin and styrene / maleic acid half ester resin are preferred. The softening point of these resins should be selected in the range of 40 ° C to 150 ° C. If the temperature exceeds 150 ° C, the thermal recording sensitivity will be low, while the other 4
If it is less than 0 ° C, the adhesion resistance is poor.
【0021】熱接着層の厚みは、0.1μmから20μ
mが好ましく、0.1μmより薄いとインキの受容性が
悪く、20μmより厚いと熱接着層を塗布乾燥する時に
溶剤の乾燥負荷が大きくなる。The thickness of the heat-bonding layer is 0.1 μm to 20 μm.
m is preferable, and if it is thinner than 0.1 μm, the ink receptivity is poor, and if it is thicker than 20 μm, the drying load of the solvent increases when the thermal adhesive layer is applied and dried.
【0022】熱熱接着層を設ける受像シート用支持体と
しては、各種合成紙を好ましく用いることができ、各種
顔料を充填させた合成紙やプラスチックを発泡させた合
成紙やプラスチックを発泡させた合成紙の上に顔料を充
填させた層を有する合成紙等業界公知の様々な合成紙を
使用でき、素材としてはポリエステル系合成紙,ポリエ
チレン系合成紙,ポリプロピレン系合成紙等の各種プラ
スチックフイルム等を用いることができる。ポリエステ
ル系合成紙としては、白色ポリエステル;例えば、K1
553(東洋紡株式会社製)やE20、E68L(東レ
株式会社製)やW900(ダイアホイル株式会社製)や
Melinex−470(ICI株式会社製)やCar
ifil(Shell株式会社製)やピーチコート(日
清紡績株式会社製)等を好ましく用いることができ、ポ
リプロピレン系合成紙としてはP4256(東洋紡株式
会社製)やユポ(王子油化合成紙株式会社製)やピーチ
コート(日清紡績株式会社製)等を好ましく用いること
が出来、ポリエチレン系合成紙としてはTYVEK(D
upont株式会社製)等を好ましく用いることができ
いる。これらの合成紙の中では、耐熱性の観点からポリ
エステル系合成紙を特に好ましく用いる事ができ、ポリ
エステル系合成紙の中では、サーマルヘッドへに均一に
接触できる事とゴミ等の障害に強い点で発泡ポリエステ
ル合成紙;例えばE−68L(東レ株式会社製)が特に
好ましい。As the support for the image-receiving sheet provided with the heat-and-heat adhesive layer, various synthetic papers can be preferably used, and synthetic papers filled with various pigments, synthetic papers obtained by foaming plastics or synthetics obtained by foaming plastics. Various synthetic papers known in the industry such as synthetic paper having a layer filled with pigment on the paper can be used, and various plastic films such as polyester synthetic paper, polyethylene synthetic paper and polypropylene synthetic paper can be used as materials. Can be used. As the polyester synthetic paper, white polyester; for example, K1
553 (manufactured by Toyobo Co., Ltd.), E20, E68L (manufactured by Toray Co., Ltd.), W900 (manufactured by Diafoil Co., Ltd.), Melinex-470 (manufactured by ICI Co., Ltd.), Car.
Ifil (manufactured by Shell Co., Ltd.), peach coat (manufactured by Nisshinbo Industries Co., Ltd.) or the like can be preferably used, and as the polypropylene-based synthetic paper, P4256 (manufactured by Toyobo Co., Ltd.) or YUPO (manufactured by Oji Yuka Synthetic Paper Co., Ltd.). Peach coat (manufactured by Nisshinbo Industries, Inc.) and the like can be preferably used, and TYVEK (D
Upton Co., Ltd.) and the like can be preferably used. Among these synthetic papers, polyester-based synthetic paper can be particularly preferably used from the viewpoint of heat resistance, and among the polyester-based synthetic papers, uniform contact with the thermal head and strong resistance to dust and the like are required. Particularly preferred is foamed polyester synthetic paper; for example, E-68L (manufactured by Toray Industries, Inc.).
【0023】本発明においては、インキ層や熱接着層等
の各層に界面活性剤を含有していてもよく、界面活性剤
としては、業界公知の様々な界面活性剤が使用でる。例
えば、脂肪酸塩類、高級アルコール硫酸エステル塩類、
脂肪族アミンもしくは脂肪族アミドの硫酸塩類、脂肪族
アルコール燐酸エステル塩類、二塩基性脂肪酸エステル
のスルホン酸塩類、脂肪族アミドスルホン酸塩類、アル
キルアリルスルホン酸塩類、ホルマリン縮合のナフタレ
ンスルホン酸塩類等のアニオン系界面活性剤、脂肪族ア
ミン塩類、第四級アンモニウム塩類、アルキルピリジニ
ウム塩類等のカチオン系界面活性剤、ポリオキシエチレ
ンアルキルエーテル類、ポリオキシエチレンアルキルフ
ェノールエーテル類、ポリオキシエチレンアルキルエス
テル類、ソルビタンアルキルエステル類、ポリオキシエ
チレンソルビタンアルキルエステル類等の非イオン系界
面活性剤、カルボン酸誘導体、イミダゾリン誘導体等の
両性界面活性剤等が挙げられる。In the present invention, each layer such as the ink layer and the heat adhesive layer may contain a surfactant, and various surfactants known in the art can be used as the surfactant. For example, fatty acid salts, higher alcohol sulfate ester salts,
Such as aliphatic amine or aliphatic amide sulfates, aliphatic alcohol phosphate ester salts, dibasic fatty acid ester sulfonates, aliphatic amide sulfonates, alkylallyl sulfonates, formalin-condensed naphthalene sulfonates, etc. Cationic surfactants such as anionic surfactants, aliphatic amine salts, quaternary ammonium salts, alkylpyridinium salts, polyoxyethylene alkyl ethers, polyoxyethylene alkylphenol ethers, polyoxyethylene alkyl esters, sorbitan Examples thereof include nonionic surfactants such as alkyl esters and polyoxyethylene sorbitan alkyl esters, and amphoteric surfactants such as carboxylic acid derivatives and imidazoline derivatives.
【0024】更に、本発明においては、フッ素系界面の
活性剤を用いることが好ましく、例えば、パーフルオロ
アルキルカルボン酸類、フルオロ脂肪族基含有アクリレ
ートもしくはフルオロ脂肪族基含有メタクリレートとポ
リオキシアルキレンアクリレートもしくはポリオキシア
ルキレンメタクリレートとの共重合体、パーフルオロア
ルキルスルホンアミド類等が挙げられる。これらの中
で、フルオロ脂肪族基含有アクリレートもしくはフルオ
ロ脂肪族基含有メタクリレートとポリオキシアルキレン
アクリレートもしくはポリオキシアルキレンメタクリレ
ートとの共重合体がより好ましい。Further, in the present invention, it is preferable to use a fluorochemical surfactant, for example, perfluoroalkylcarboxylic acids, fluoroaliphatic group-containing acrylate or fluoroaliphatic group-containing methacrylate and polyoxyalkylene acrylate or polyoxyalkylene acrylate or polyoxyalkylene acrylate or polyoxyalkylene acrylate. Examples thereof include copolymers with oxyalkylene methacrylate and perfluoroalkyl sulfonamides. Among these, a copolymer of fluoroaliphatic group-containing acrylate or fluoroaliphatic group-containing methacrylate and polyoxyalkylene acrylate or polyoxyalkylene methacrylate is more preferable.
【0025】界面活性剤の添加量は、各層の素材に対し
て0.001〜10重量%であるが、より好ましくは
0.01〜5重量%である。10重量%を超えると、ド
ット形状が著しく悪化し、再現階調性も悪化してしまう
事がある。また、添加量が0.001重量%に満たない
場合には、塗布面状が悪化し、保存時の温湿度依存性も
悪化してしまう。The amount of the surfactant added is 0.001 to 10% by weight, and more preferably 0.01 to 5% by weight, based on the material of each layer. If it exceeds 10% by weight, the dot shape may be remarkably deteriorated and the reproduction gradation may be deteriorated. Further, if the addition amount is less than 0.001% by weight, the coated surface state deteriorates and the temperature-humidity dependency during storage also deteriorates.
【0026】本発明の感熱転写記録材料の支持体として
は、従来の溶融転写や昇華転写用支持体として公知の種
々の支持体が使用されるが、通常のサーマルヘッド転写
感材と同様に厚み5μm前後の裏面に離型処理をほどこ
したポリエステルフイルムが特に好ましい。As the support for the heat-sensitive transfer recording material of the present invention, various supports known as conventional melt transfer or sublimation transfer supports are used. A polyester film having a back surface of about 5 μm and subjected to a release treatment is particularly preferable.
【0027】本発明の記録材料には、これまで述べた添
加剤を含め必要に応じて様々な添加剤を添加することが
できる。例えば、紫外線吸収剤、可塑剤、蛍光増白剤、
マット剤、塗布助剤、硬化剤、帯電防止剤や滑り性改良
剤等の代表例はResearch Disclosur
e,Vol.176,1978年12月,Item17
643、および同 Vo l.187,1979年11
月,Item 18716 に記載されている。Various additives can be added to the recording material of the present invention, if necessary, including the additives described above. For example, UV absorbers, plasticizers, optical brighteners,
Typical examples of matting agents, coating aids, curing agents, antistatic agents and slipperiness improving agents are Research Disclosure.
e, Vol. 176, December 1978, Item 17
643, and Vol. 187, 1979 11
Mon, Item 18716.
【0028】本発明の記録材料の各層用の塗布液は所望
の支持体上に塗布し、乾燥することにより本発明の記録
材料が得られる。その場合に使用される溶媒としては、
水、アルコール:例えばメタノール、エタノール,n−
プロパノール、イソプロパノール、n−ブタノール、s
ec−ブタノール、メチルセロソルブ、1−メトキシ−
2−プロパノール;ハロゲン系の溶剤:例えばメチレン
クロライド、エチレンクロライド;ケトン:例えばアセ
トン、シクロヘキサノン、メチルエチルケトン;エステ
ル:例えば、酢酸メチルセロソルブ、酢酸エチル、酢酸
メチル;トルエン、キシレン等の単独物及びそれらの2
種以上の混合物を例として挙げることができる。The coating material for each layer of the recording material of the present invention is applied onto a desired support and dried to obtain the recording material of the present invention. In that case, as the solvent used,
Water, alcohol: for example, methanol, ethanol, n-
Propanol, isopropanol, n-butanol, s
ec-butanol, methyl cellosolve, 1-methoxy-
2-Propanol; Halogen-based solvent: for example, methylene chloride, ethylene chloride; Ketone: for example, acetone, cyclohexanone, methyl ethyl ketone; Ester: for example, methyl cellosolve acetate, ethyl acetate, methyl acetate; toluene, xylene and the like alone and two of them.
A mixture of more than one species can be mentioned as an example.
【0029】各層用の塗布液を支持体上に塗布するに
は、ブレードコーター、ロッドコーター、ナイフコータ
ー、ロールドクターコーター、リバースロールコータ
ー、トランスファーロールコーター、グラビアコータ
ー、キスロールコーター、カーテンコーター、エクスト
ルージョンコーター等を用いることができる。塗布方法
としてはResearch Disclosure,V
ol.200,1980年12月,Item 2003
6 XV項を参考にできる。塗布は単層塗布、逐次重層
塗布、同時重層塗布のいずれの方法をとってもよい。各
記録層の厚みとしては、0.1μmから50μmが適当
である。To apply the coating liquid for each layer onto the support, a blade coater, a rod coater, a knife coater, a roll doctor coater, a reverse roll coater, a transfer roll coater, a gravure coater, a kiss roll coater, a curtain coater, an ext. A rouge coater or the like can be used. As a coating method, Research Disclosure, V
ol. 200, December 1980, Item 2003
You can refer to Section 6 XV. The coating may be carried out by any of single layer coating, sequential multilayer coating and simultaneous multilayer coating. The appropriate thickness of each recording layer is 0.1 μm to 50 μm.
【0030】熱転写を行う熱プリンターとしては、業界
公知の各種昇華転写プリンターや溶融転写プリンター等
のサーマルヘッド搭載のサーマルプリンターやアプルー
バル(イーストマンコダック株式会社製)等のヒートモ
ードレーザープリンターを使用できる。熱ヘッドにて該
受像シートに感熱転写画像を形成した該感熱転写画像を
印刷本紙と重ね合わせ加熱・加圧し感熱転写画像を印刷
本紙上に転写する装置としては、各種ラミネーターが使
用でき、加熱温度としては60℃から200℃が好まし
く、80℃〜180℃が特に好ましい。加圧の線圧とし
て特に限定はないが、1g/cm2から1000Kg/
cm2の範囲の圧力が好ましく、100g/cm2から1
0Kg/cm2が特に好ましい。また、受像シート上の
画像を用いる時には、正像を印字する事が好ましく、印
刷本紙上に転写して画像を用いるときには左右逆像をプ
リンターで印字する事が好ましい。As a thermal printer for performing thermal transfer, a thermal printer equipped with a thermal head such as various sublimation transfer printers and melt transfer printers known in the industry, and a heat mode laser printer such as Approval (produced by Eastman Kodak Co., Ltd.) can be used. A thermal transfer image is formed on the image-receiving sheet with a thermal head. The laminator can be used as a device for transferring the heat-sensitive transfer image onto the main printing paper by superposing and heating the heat-sensitive transfer image on the main printing paper. Is preferably from 60 ° C to 200 ° C, particularly preferably from 80 ° C to 180 ° C. The linear pressure for pressing is not particularly limited, but is 1 g / cm 2 to 1000 kg /
Pressures in the cm 2 range are preferred, 100 g / cm 2 to 1
0 kg / cm 2 is particularly preferred. Further, when the image on the image receiving sheet is used, it is preferable to print a normal image, and when the image is transferred onto the actual printing paper to use the image, it is preferable to print a left-right reversed image with a printer.
【0031】以下に本発明の実施例を示すが、本発明は
これに限定されるものではない。Examples of the present invention will be shown below, but the present invention is not limited thereto.
【0032】[0032]
実施例1 (感熱転写材料の作成)下記の組成を有する3種のイン
キ層用塗布液を調製した。 1.イエローインクシートの作成 下記の組成物をボールミルで分散し、面積基準平均粒径
(ホリバ社製LA700による)が0.23μmになる
ようにインク層用塗布液を作成した。 ・ポリビニルブチラール 12重量部 (デンカブチラール#2000−L,電気化学工業(株)製) ・イエロー顔料(C.I.PY.14) 12重量部 ・分散助剤 0.8重量部 (ソルスパースS−20000,ICIジャパン(株)製) ・溶剤 n−プロピルアルコール 110重量部Example 1 (Preparation of heat-sensitive transfer material) Three types of ink layer coating solutions having the following compositions were prepared. 1. Preparation of Yellow Ink Sheet The following composition was dispersed by a ball mill to prepare an ink layer coating solution so that the area-based average particle diameter (by LA700 manufactured by Horiba Ltd.) was 0.23 μm. -Polyvinyl butyral 12 parts by weight (Denka Butyral # 2000-L, manufactured by Denki Kagaku Kogyo Co., Ltd.)-Yellow pigment (CI.PY.14) 12 parts by weight-Dispersion aid 0.8 parts by weight (Solspers S- 20000, manufactured by ICI Japan Co., Ltd.-Solvent n-propyl alcohol 110 parts by weight
【0033】上記の液10重量部に対し、N−ヒドロキ
シエチル−12−ヒドロキシステアリン酸アミド0.2
4重量部,界面活性剤(メガファックF−177、大日
本インキ化学工業(株)製)0.01重量部,n−プロピ
ルアルコール60重量部を加え塗布液とし、厚み5μm
の裏面に離型処理されたポリエステルフィルム(帝人
(株)製)に回転塗布機(ホワイラー)を使用して、乾
燥膜厚が0.36μmになるように塗布しイエローイン
クシートを得た。0.2 parts of N-hydroxyethyl-12-hydroxystearic acid amide was added to 10 parts by weight of the above liquid.
4 parts by weight, 0.01 parts by weight of a surfactant (MegaFac F-177, manufactured by Dainippon Ink and Chemicals, Inc.) and 60 parts by weight of n-propyl alcohol were added to form a coating solution, and the thickness was 5 μm.
A polyester film (manufactured by Teijin Ltd.) having a release treatment on its back surface was coated with a spin coater (Wheeler) to a dry film thickness of 0.36 μm to obtain a yellow ink sheet.
【0034】2.マゼンタインクシートの作成 顔料をマゼンタ顔料(C.I.PR.57:1)に変更し
た以外はイエローインクシートと同様の操作を行い乾燥
膜厚が0.38μmのマゼンタインクシートを得た。2. Preparation of Magenta Ink Sheet A magenta ink sheet having a dry film thickness of 0.38 μm was obtained by performing the same operation as that of the yellow ink sheet except that the pigment was changed to a magenta pigment (C.I.PR. 57: 1).
【0035】3.シアンインクシートの作成 顔料をシアン顔料(C.I.PB.15:4)に変更した
以外はイエローインクシートと同様の操作を行い透乾燥
膜厚が0.42μmのシアンインクシートを得た。3. Preparation of Cyan Ink Sheet A cyan ink sheet having a transmissive dry film thickness of 0.42 μm was obtained by performing the same operation as that of the yellow ink sheet except that the pigment was changed to a cyan pigment (CI.PB.15: 4).
【0036】4.黒シートの作成 顔料をカーボンブラック(C.I.P.B.7)に変更
し、更に量を16重量部た以外はイエローインクシート
と同様の操作を行い乾燥膜厚が0.44μmになるよう
に塗布した。4. Preparation of black sheet The same operation as the yellow ink sheet is performed except that the pigment is changed to carbon black (CIPB7) and the amount is 16 parts by weight, and the dry film thickness is 0.44 μm. As applied.
【0037】(受像シートの作成)下記の組成を有する
受像第一層及び熱接着層の塗布液を調製した。 <受像第一層用塗布液> ・塩ビ/酢ビ共重合体 25重量部 (MPR−TSL,日信化学(株)製) ・ジオクチルフタレート 12重量部 (DOP,大八化学(株)製) ・界面活性剤 4重量部 (メガファックF−177,大日本インキ化学工業(株)製) ・溶剤 メチルエチルケトン 75重量部(Preparation of Image Receiving Sheet) A coating solution for the image receiving first layer and the heat-adhesive layer having the following composition was prepared. <Coating liquid for first layer of image receiving> 25 parts by weight of vinyl chloride / vinyl acetate copolymer (MPR-TSL, manufactured by Nissin Chemical Co., Ltd.) 12 parts by weight of dioctyl phthalate (DOP, manufactured by Daihachi Chemical Co., Ltd.)・ Surfactant 4 parts by weight (MegaFac F-177, manufactured by Dainippon Ink and Chemicals, Inc.) ・ Solvent Methyl ethyl ketone 75 parts by weight
【0038】 <熱接着層用塗布液> ・ポリビニルブチラール 16重量部 (デンカブチラール#2000−L,電気化学工業(株)製) ・N,N−ジメチルアクリルアミド/ブチルアクリレート共重合体 4重量部 ・界面活性剤 0.5重量部 (メガファックF−177,大日本インキ化学工業(株)製) ・溶剤 n−プロピルアルコール 200重量部<Coating Liquid for Thermal Adhesive Layer> 16 parts by weight of polyvinyl butyral (Denka Butyral # 2000-L, manufactured by Denki Kagaku Kogyo Co., Ltd.) 4 parts by weight of N, N-dimethylacrylamide / butyl acrylate copolymer Surfactant 0.5 parts by weight (MegaFac F-177, Dainippon Ink and Chemicals, Inc.)-Solvent n-propyl alcohol 200 parts by weight
【0039】厚さ135μmの白色ポリエステル支持体
(E−68L;東レ株式会社製)上に、回転塗布機を使
用して上記受像第一層用塗布液を塗布し、100℃のオ
ーブン中で2分間乾燥した。得られた受像第一層の膜厚
は20μmであった。更に上記受像第一層上に、回転塗
布機を使用して熱接着層用塗布液を塗布し、100℃の
オーブン中で2分間乾燥した。得られた熱接着層の膜厚
は2μmであった。A white polyester support (E-68L; manufactured by Toray Industries, Inc.) having a thickness of 135 μm was coated with the coating solution for the first image-receiving layer using a spin coater, and the coating solution was placed in an oven at 100 ° C. for 2 minutes. Dry for minutes. The thickness of the obtained first image receiving layer was 20 μm. Further, the coating solution for heat-adhesive layer was applied onto the first image receiving layer using a spin coater, and dried in an oven at 100 ° C. for 2 minutes. The film thickness of the obtained thermal adhesive layer was 2 μm.
【0040】まずシアンの感熱転写材料と受像シートを
重ね、副走査分割法によるサーマルヘッド記録装置によ
り左右逆像を印字した。この原理は75μm×50μm
のヘッドを50μm方向に微小送り3μmピッチでオン
オフすることにより、面積階調のみの多段階変調を行う
方式である。このシアンの感熱転写材料のポリエステル
フィルムを剥離し、受像シート上に面積階調のみよりな
る画像を形成させた。次にマゼンタの感熱転写材料をシ
アン画像が形成されている受像シート上に重ね、位置を
合わせて同様に印字し、該転写材料のポリエステルフィ
ルムを剥離することにより受像シート上にマゼンタ画
像、さらに同様にしてイエロー画像、ブラック画像を形
成させ、受像シート上に面積階調のみよりなるカラー画
像を形成させた。このカラー画像は、リス原稿から作成
したケミカルプルーフ(カラーアート,富士写真フィル
ム(株)製)とカラー画像の近似性が非常に良好であっ
た。なおこの際の各単色の反射濃度は下記の通りであ
る。 また4Pの文字の濃度をミクロデンシトメーターで測定
したが、ベタ部の濃度と同様であった。また階調再現性
は5〜95%が再現され、ゴミによる欠陥、にじみによ
るドット形状の不良もなく良好であった。First, the heat-sensitive transfer material for cyan and the image-receiving sheet were superposed on each other, and the right and left reverse images were printed by the thermal head recording device by the sub-scanning division method. This principle is 75μm × 50μm
This is a method of performing multi-step modulation only for area gradation by turning on and off the head in the direction of 50 μm in a minute feed at a pitch of 3 μm. The polyester film of the cyan heat-sensitive transfer material was peeled off to form an image consisting of only area gradation on the image receiving sheet. Next, a magenta heat-sensitive transfer material is superposed on an image-receiving sheet on which a cyan image is formed, aligned and printed in the same manner, and the polyester film of the transfer material is peeled off to form a magenta image on the image-receiving sheet, and then the same. Then, a yellow image and a black image were formed, and a color image consisting only of area gradation was formed on the image receiving sheet. This color image was very close to the chemical proof (Color Art, manufactured by Fuji Photo Film Co., Ltd.) made from the lith original, and the color image was very close to each other. The reflection densities of the respective monochromatic colors at this time are as follows. The density of 4P characters was measured with a microdensitometer, and it was the same as the density of solid areas. Further, the gradation reproducibility was 5 to 95%, and there was no defect due to dust and no dot shape defect due to bleeding, which was good.
【0041】この印字は約10分で、迅速に画像が得ら
れた。しかし、画像自体の濃度・色相は印刷に近似して
いたが、印刷本紙がやや黄色がかっているのに反し地肌
は白く、また、印刷では表面光沢が少ないがこの画像表
面は非常に平滑で、外観的には印刷とやや異なる画像で
あった。This printing took about 10 minutes, and an image was quickly obtained. However, the density and hue of the image itself was similar to that of printing, but the printing paper is slightly yellowish, but the background is white, and the surface gloss is small in printing, but this image surface is very smooth, The appearance was slightly different from the printed image.
【0042】実施例2 (印刷本紙への転写)次にこのカラー画像が形成された
受像シートをアート紙と重ね、4.5Kg/cm2の圧
力,130℃,4m/secのスピードで熱ローラーを通
した後、受像シートの白色ポリエステル支持体を剥が
し、インク画像がのった熱接着層をアート紙上に転写し
カラー画像形成させた。このカラー画像は、リス原稿か
ら作成したケミカルプルーフ(カラーアート,富士写真
フィルム(株)製)とカラー画像の近似性が非常に良好
であった。更に紙の凹凸に追随して表面がマット化さ
れ、表面光沢、手触りが印刷物に非常に近似した画像で
あった。この本紙への転写には約1分を要した。Example 2 (Transfer to actual printing paper) Next, the image-receiving sheet on which this color image was formed was superposed on art paper, and a heat roller was applied at a pressure of 4.5 Kg / cm 2 , 130 ° C. and a speed of 4 m / sec. After passing through the sheet, the white polyester support of the image receiving sheet was peeled off, and the thermal adhesive layer bearing the ink image was transferred onto art paper to form a color image. This color image was very close to the chemical proof (Color Art, manufactured by Fuji Photo Film Co., Ltd.) made from the lith original, and the color image was very close to each other. Furthermore, the surface was matted following the irregularities of the paper, and the surface gloss and touch were very similar to those of printed matter. It took about 1 minute to transfer to the actual paper.
【0043】比較例1 市販の昇華転写記録装置・昇華転写記録用トナーシート
・昇華転写記録用の専用紙を用い、実施例1と同じ電子
画像を印画した。印画時間は、実施例1と同様約10分
であったが、画像の表面は平滑で・地肌は印刷本紙より
白く、外観的には印刷と大きく異なっていた。Comparative Example 1 The same electronic image as in Example 1 was printed using a commercially available sublimation transfer recording device, a toner sheet for sublimation transfer recording, and a dedicated paper for sublimation transfer recording. The printing time was about 10 minutes as in Example 1, but the surface of the image was smooth and the background was whiter than the actual printing paper, and the appearance was significantly different from the printing.
【0044】[0044]
【発明の効果】本発明によって、従来の昇華染料感熱転
写方式や溶融転写方式では実現出来なかった印刷用プル
ーフに適した、高画質の画像を迅速に得る事ができ、更
に、印刷本紙上に画像が形成できるので、印刷本紙に由
来する微妙な色調や紙質感も判断できた。得られた画像
のエッジシャープネスも含めたドット形状は良好で、階
調再現性に優れ、印刷物近似性に優れていた。According to the present invention, it is possible to quickly obtain a high-quality image suitable for a printing proof, which could not be realized by the conventional sublimation dye thermal transfer method or melt transfer method, and further, on the actual printing paper. Since an image can be formed, it was possible to judge the subtle color tone and paper texture derived from the actual printing paper. The dot shape including the edge sharpness of the obtained image was good, the gradation reproducibility was excellent, and the printed matter approximation was excellent.
Claims (1)
ートを用い、30〜70重量部の顔料と25〜60重量
部の軟化点が40℃〜150℃の有機高分子重合体を含
み、膜厚が0.2μm〜1.0μmの範囲に有る感熱イ
ンキ層を有し、該感熱インキ層中の顔料の70%以上の
粒径が1.0μm以下であり、かつ転写画像の光学反射
濃度が白色支持体上で1.0以上有る感熱転写記録材料
の裏面から熱ヘッドにて該受像シートにインキ層を感熱
転写し感熱転写画像を形成させる第一の方法と、該感熱
転写画像を印刷本紙と重ね合わせ少なくとも加圧するこ
とにより該感熱転写画像を印刷本紙上に転写して画像を
形成する第二の方法の何れかを選択する事を特徴とする
感熱転写記録の方法。1. An image receiving sheet having a heat-adhesive layer on a white support, comprising 30 to 70 parts by weight of a pigment and 25 to 60 parts by weight of an organic polymer having a softening point of 40 ° C. to 150 ° C. A heat-sensitive ink layer having a film thickness in the range of 0.2 μm to 1.0 μm, 70% or more of the pigments in the heat-sensitive ink layer have a particle size of 1.0 μm or less, and the optical reflection of a transferred image A first method of forming a heat-sensitive transfer image by heat-transferring an ink layer from the back surface of a heat-sensitive transfer recording material having a density of 1.0 or more on a white support to the image-receiving sheet with a thermal head, and the heat-sensitive transfer image. A method of heat-sensitive transfer recording, which comprises selecting one of the second methods of forming an image by transferring the heat-sensitive transfer image onto the printing main paper by superposing it on the printing main paper and at least applying pressure.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7100915A JPH08290683A (en) | 1995-04-25 | 1995-04-25 | Heat-sensitive transfer recording method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7100915A JPH08290683A (en) | 1995-04-25 | 1995-04-25 | Heat-sensitive transfer recording method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH08290683A true JPH08290683A (en) | 1996-11-05 |
Family
ID=14286641
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7100915A Pending JPH08290683A (en) | 1995-04-25 | 1995-04-25 | Heat-sensitive transfer recording method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH08290683A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002234203A (en) * | 2001-02-13 | 2002-08-20 | Toppan Printing Co Ltd | Imaging body and imaging method |
-
1995
- 1995-04-25 JP JP7100915A patent/JPH08290683A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002234203A (en) * | 2001-02-13 | 2002-08-20 | Toppan Printing Co Ltd | Imaging body and imaging method |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3720396B2 (en) | Thermal transfer recording material | |
US5726122A (en) | Thermal transfer image receiving sheet, production process therefor and thermal transfer sheet | |
JP3204820B2 (en) | Thermal transfer recording material and image forming method | |
JPH08332782A (en) | Dye accepting element containing elastic bead in protective coat layer for thermosensible dye transfer | |
JPH0911651A (en) | Thermal transfer image receiving sheet and image forming method | |
JPH08290676A (en) | Thermal transfer sheet and image forming method | |
JPH08290683A (en) | Heat-sensitive transfer recording method | |
JP3020380B2 (en) | Thermal transfer recording medium | |
JPH08197862A (en) | Image receiving sheet material and transfer image forming method | |
JPH08112969A (en) | Thermal transfer recording material | |
JP3685826B2 (en) | Thermal transfer recording material | |
JPH07172074A (en) | Transfer medium and thermal transfer recording method | |
JPH0976649A (en) | Thermal transfer type recording material | |
JPH08290678A (en) | Thermal transfer sheet and image forming method | |
US5518985A (en) | Image receiving material for thermal dye transfer | |
JPH08290674A (en) | Method for forming ohp image | |
JP2986722B2 (en) | Thermal transfer sheet | |
JP2003165278A (en) | Thermal transfer film and thermal transfer recording medium | |
JP3629063B2 (en) | Thermal transfer sheet and image forming method | |
JP3254569B2 (en) | Thermal transfer image receiving sheet | |
JPH08290680A (en) | Image forming method | |
JPH11165472A (en) | Thermal transfer sheet | |
JPH11157219A (en) | Thermal transfer ink ribbon | |
JPH11180059A (en) | Thermal-transfer ink ribbon, image-receiving sheet material, and image formation | |
JPH0858253A (en) | Image receiving sheet material, transfer image forming method and laminate |