JPH03126589A - Thermal transfer dye donating material - Google Patents
Thermal transfer dye donating materialInfo
- Publication number
- JPH03126589A JPH03126589A JP1264777A JP26477789A JPH03126589A JP H03126589 A JPH03126589 A JP H03126589A JP 1264777 A JP1264777 A JP 1264777A JP 26477789 A JP26477789 A JP 26477789A JP H03126589 A JPH03126589 A JP H03126589A
- Authority
- JP
- Japan
- Prior art keywords
- dye
- thermal transfer
- layer
- binder
- resin
- 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 91
- 239000000463 material Substances 0.000 title claims description 88
- 239000011230 binding agent Substances 0.000 claims abstract description 23
- 229920005989 resin Polymers 0.000 abstract description 33
- 239000011347 resin Substances 0.000 abstract description 33
- 238000000034 method Methods 0.000 abstract description 16
- 239000002904 solvent Substances 0.000 abstract description 12
- 229920001225 polyester resin Polymers 0.000 abstract description 7
- 239000004645 polyester resin Substances 0.000 abstract description 7
- 229920006122 polyamide resin Polymers 0.000 abstract description 3
- 238000004321 preservation Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 70
- 239000000975 dye Substances 0.000 description 41
- -1 polyethylene Polymers 0.000 description 35
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 18
- 239000000123 paper Substances 0.000 description 17
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 13
- 229920002545 silicone oil Polymers 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 108010010803 Gelatin Proteins 0.000 description 9
- 229920000159 gelatin Polymers 0.000 description 9
- 235000019322 gelatine Nutrition 0.000 description 9
- 235000011852 gelatine desserts Nutrition 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- 239000008273 gelatin Substances 0.000 description 8
- 239000004848 polyfunctional curative Substances 0.000 description 8
- 239000003232 water-soluble binding agent Substances 0.000 description 8
- 238000009792 diffusion process Methods 0.000 description 7
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 7
- 229920001296 polysiloxane Polymers 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000008199 coating composition Substances 0.000 description 6
- 238000005562 fading Methods 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 229920000098 polyolefin Polymers 0.000 description 6
- 229920002451 polyvinyl alcohol Polymers 0.000 description 6
- 229920003002 synthetic resin Polymers 0.000 description 6
- 239000000057 synthetic resin Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 229920002125 Sokalan® Polymers 0.000 description 5
- 229920002678 cellulose Polymers 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 239000011737 fluorine Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 229920003169 water-soluble polymer Polymers 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000007639 printing Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 229920002301 cellulose acetate Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 150000002222 fluorine compounds Chemical class 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000006082 mold release agent Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 150000003014 phosphoric acid esters Chemical class 0.000 description 3
- 229920005668 polycarbonate resin Polymers 0.000 description 3
- 239000004431 polycarbonate resin Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920001228 polyisocyanate Polymers 0.000 description 3
- 239000005056 polyisocyanate Substances 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000010365 information processing Effects 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000006224 matting agent Substances 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000001454 recorded image Methods 0.000 description 2
- 239000012508 resin bead Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- NJVOHKFLBKQLIZ-UHFFFAOYSA-N (2-ethenylphenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1C=C NJVOHKFLBKQLIZ-UHFFFAOYSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- QLSZKZBYTNPFKZ-UHFFFAOYSA-N 1,1-dichloroethene;prop-2-enenitrile;prop-2-enoic acid Chemical compound C=CC#N.ClC(Cl)=C.OC(=O)C=C QLSZKZBYTNPFKZ-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- YGDWUQFZMXWDKE-UHFFFAOYSA-N 1-oxido-1,3-thiazole Chemical class [O-]S1=CN=C=C1 YGDWUQFZMXWDKE-UHFFFAOYSA-N 0.000 description 1
- HBEDSQVIWPRPAY-UHFFFAOYSA-N 2,3-dihydrobenzofuran Chemical class C1=CC=C2OCCC2=C1 HBEDSQVIWPRPAY-UHFFFAOYSA-N 0.000 description 1
- DGBZCCXQJHOSMY-UHFFFAOYSA-N 2-aminoethyl 2-methylprop-2-enoate;butyl prop-2-enoate;2-hydroxyethyl 2-methylprop-2-enoate Chemical compound CCCCOC(=O)C=C.CC(=C)C(=O)OCCN.CC(=C)C(=O)OCCO DGBZCCXQJHOSMY-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- KTSDQEHXNNLUEA-UHFFFAOYSA-N 2-ethenylsulfonylacetamide Chemical compound NC(=O)CS(=O)(=O)C=C KTSDQEHXNNLUEA-UHFFFAOYSA-N 0.000 description 1
- CBECDWUDYQOTSW-UHFFFAOYSA-N 2-ethylbut-3-enal Chemical group CCC(C=C)C=O CBECDWUDYQOTSW-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- FWBHETKCLVMNFS-UHFFFAOYSA-N 4',6-Diamino-2-phenylindol Chemical compound C1=CC(C(=N)N)=CC=C1C1=CC2=CC=C(C(N)=N)C=C2N1 FWBHETKCLVMNFS-UHFFFAOYSA-N 0.000 description 1
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-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
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- GAMPNQJDUFQVQO-UHFFFAOYSA-N acetic acid;phthalic acid Chemical compound CC(O)=O.OC(=O)C1=CC=CC=C1C(O)=O GAMPNQJDUFQVQO-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000007611 bar coating method Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical class C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical class C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000000332 coumarinyl group Chemical class O1C(=O)C(=CC2=CC=CC=C12)* 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 125000000687 hydroquinonyl group Chemical class C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- GVDMJXQHPUYPHP-FYQPLNBISA-N norgestrienone Chemical compound C1CC(=O)C=C2CC[C@@H]([C@H]3[C@@](C)([C@](CC3)(O)C#C)C=C3)C3=C21 GVDMJXQHPUYPHP-FYQPLNBISA-N 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
- 229950005308 oxymethurea Drugs 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920003172 poly (isopropyl acrylamide) Polymers 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920006350 polyacrylonitrile resin Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- FUPZEKMVZVPYLE-UHFFFAOYSA-N prop-2-enoic acid;prop-2-enylbenzene Chemical compound OC(=O)C=C.C=CCC1=CC=CC=C1 FUPZEKMVZVPYLE-UHFFFAOYSA-N 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical class C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000007651 thermal printing Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は熱転写色素供与材料に関するものであり、特に
低エネルギーで高濃度の熱転写が可能でかつ保存中に安
定性に優れた熱転写色素供与材料に関するものである。Detailed Description of the Invention (Industrial Application Field) The present invention relates to a thermal transfer dye-providing material, and in particular a thermal transfer dye-providing material that is capable of high-density thermal transfer with low energy and has excellent stability during storage. It is related to.
(背景技術)
近年、情報産業の急速な発展に伴い、種々の情報処理シ
ステムが開発され、またそれぞれの情報処理システムに
通した記録方法および装置も開発、採用されている。こ
のような記録方法の一つとして熱転写記録方法は、使用
する装置が軽量かつコンパクトで騒音がなく、操作性、
保守性にも優れており、カラー化も容易であり、最近法
(使用されている。熱転写記録方法は支持体上にバイン
ダーと熱移行性色素を含有する色素供与層を有する熱転
写色素供与材料を熱転写受像材料と重ね合わせて、色素
供与材料の支持体側から熱印加し、熱印加したパターン
杖に熱移行性色素を記録媒体(熱転写受像材料)に転写
させて転写像を得る方法である。(Background Art) In recent years, with the rapid development of the information industry, various information processing systems have been developed, and recording methods and devices for each information processing system have also been developed and adopted. The thermal transfer recording method is one of these recording methods.The equipment used is lightweight, compact, noiseless, easy to operate,
It has excellent maintainability and is easy to color.Thermal transfer recording method uses a thermal transfer dye-providing material that has a dye-donating layer containing a binder and a heat-transferable dye on a support. In this method, heat is applied from the support side of the dye-providing material by superimposing it on a thermal transfer image-receiving material, and the heat-transferable dye is transferred to the recording medium (thermal transfer image-receiving material) using the pattern rod to which the heat is applied, thereby obtaining a transferred image.
なお、ここで熱移行性の色素とは、昇華または媒体中で
の拡散により熱転写色素供与材料から熱転写受像材料へ
転写しうる色素をいう。Note that the term "thermally transferable dye" as used herein refers to a dye that can be transferred from a thermal transfer dye-providing material to a thermal transfer image-receiving material by sublimation or diffusion in a medium.
(発明が解決しようとする課題)
しかし、従来この方式に用いられいる熱転写色素供与材
料は、バインダー中の色素の熱移行のために大きなエネ
ルギーを必要とし、高濃度に転写するためには高エネル
ギーを必要とした。また、バインダーを少なくすると保
存中に色素供与層中で色素の析出を生じ、画像の質を低
下させるという欠点があった。(Problem to be Solved by the Invention) However, the thermal transfer dye-providing material conventionally used in this method requires a large amount of energy for thermal transfer of the dye in the binder, and in order to transfer at high density, high energy is required. required. Furthermore, if the amount of binder is reduced, the dye will precipitate in the dye-donating layer during storage, resulting in a deterioration in image quality.
従って、低エネルギーで高濃度の熱転写が可能で、しか
も保存中の安定性に優れた熱転写色素供与材料が望まれ
ている。Therefore, there is a need for a thermal transfer dye-providing material that allows high-density thermal transfer with low energy and has excellent stability during storage.
(課題を解決するための手段)
本発明の目的は、支持体上に、少なくとも実質的に非晶
質の熱移行性色素と該色素に対して30〜100重量%
の量のバインダーを含有する色素供与層を有してなる熱
転写色素供与材料によって達成された。(Means for Solving the Problems) An object of the present invention is to coat an at least substantially amorphous heat-transferable dye on a support with an amount of 30 to 100% by weight based on the dye.
was achieved with a thermal transfer dye-donor material comprising a dye-donor layer containing an amount of binder.
以下、本発明を更に詳細に説明する。The present invention will be explained in more detail below.
本発明の熱転写色素供与材料は、支持体上に実質的に非
晶質の熱移行性色素とバインダーを含有する少なくとも
1層の色素供与層を有する熱転写色素供与材料であって
、熱印加したパターン状に色素を熱転写受像材料の受像
層に移行させて記録を行うものである0色素供与層の厚
みは乾燥膜厚で通常0.2〜5μ、特に0. 4〜2!
!の範囲に設定するのが好ましい。The thermal transfer dye-providing material of the present invention is a thermal transfer dye-providing material having at least one dye-providing layer containing a substantially amorphous heat-transferable dye and a binder on a support, the thermal transfer dye-providing material having a heat-applied pattern. The thickness of the dye-donating layer, which performs recording by transferring the dye to the image-receiving layer of the thermal transfer image-receiving material, is usually 0.2 to 5 μm in dry film thickness, particularly 0.2 to 5 μm in dry film thickness. 4~2!
! It is preferable to set it within the range of .
本発明の実質的に非晶質の熱移行性色素とは、いわゆる
一般的な融点測定法で融点を示さない色素である。ここ
で一般的な融点測定法としては日本化学会場「新実験化
学講座」第2巻87頁(丸首発行)、日本化学会場「実
験化学講座」第5巻307頁(丸首発行)に記載の方法
である。The substantially amorphous heat-transferable dye of the present invention is a dye that does not exhibit a melting point by a so-called general melting point measuring method. Here, the general method for measuring the melting point is the method described in Nippon Kagaku Kogyo's "New Experimental Chemistry Course" Volume 2, page 87 (published by Marukubi) and Nippon Kagaku Kogyo's "Experimental Chemistry Course" Volume 5, page 307 (published by Marukubi). It is.
以下に本発明に使用するに適した実質的に非晶質の熱移
行性色素を例示するが、本発明はこれに限定されるもの
ではない。Examples of substantially amorphous heat-transferable dyes suitable for use in the present invention are shown below, but the present invention is not limited thereto.
I
本発明の色素と共に用いるバインダー樹脂としては、こ
のような目的に従来公知であるバインダー樹脂のいずれ
も使用することができ、通常耐熱性が高く、しかも加熱
された場合に色素の移行を妨げないものが選択される0
例えば、ポリアミド系樹脂、ポリエステル系樹脂、エポ
キシ系樹脂、ポリウレタン系樹脂、ポリアクリル系樹脂
(例えばポリメチルメタクリレート、ポリアクリルアミ
ド、ポリスチレン−アクリロニトリル)、ポリビニルピ
ロリドンを始めとするビニル系樹脂、ポリ塩化ビニル系
樹脂(例えば塩化ビニル−酢酸ビニル共重合体)、ポリ
カーボネート系樹脂、ポリスチレン、ポリフェニレンオ
キサイド、セルロース?l’t!脂(例えばメチルセル
ロース、エチルセルロース、カルボキシメチルセルロー
ス、セルロースアセテート水素フタレート、酢酸セルロ
ース、セルロースアセテートプロピオネート、セルロー
スアセテートブチレート、セルローストリアセテート)
、ポリビニルアルコール系樹脂(例えばボビニルアルコ
ール、ポリビニルブチラールなどの部分ケン化ポリビニ
ルアルコール)、石油系樹脂、ロジン誘導体、クマロン
−インデン樹脂、テルペン系樹脂、ポリオレフィン系樹
脂(例えばポリエチレン、ポリプロピレン)などが用い
られる。I As the binder resin used with the dye of the present invention, any binder resin conventionally known for this purpose can be used, and usually has high heat resistance and does not interfere with the transfer of the dye when heated. 0 things are selected
For example, polyamide resins, polyester resins, epoxy resins, polyurethane resins, polyacrylic resins (e.g. polymethyl methacrylate, polyacrylamide, polystyrene-acrylonitrile), vinyl resins including polyvinylpyrrolidone, polyvinyl chloride resins, etc. Resin (e.g. vinyl chloride-vinyl acetate copolymer), polycarbonate resin, polystyrene, polyphenylene oxide, cellulose? L't! fats (e.g. methylcellulose, ethylcellulose, carboxymethylcellulose, cellulose acetate hydrogen phthalate, cellulose acetate, cellulose acetate propionate, cellulose acetate butyrate, cellulose triacetate)
, polyvinyl alcohol resins (e.g. partially saponified polyvinyl alcohols such as bovinyl alcohol and polyvinyl butyral), petroleum resins, rosin derivatives, coumaron-indene resins, terpene resins, polyolefin resins (e.g. polyethylene, polypropylene), etc. It will be done.
本発明において、このようなバインダー樹脂は色素10
0重量部当たり約30〜100重量部の割合で使用され
る。In the present invention, such a binder resin contains dye 10
It is used in a proportion of about 30 to 100 parts by weight per 0 parts by weight.
上記の色素およびバインダー樹脂を溶解または分散する
ためのインキ溶剤としては、従来公知のインキ溶剤が自
由に使用でき、具体的にはアルコ−ル系としてメタノー
ル、エタノール、イソプロピルアルコール、ブタノール
、イソブタノール等、ケトン系としてメチルエチルケト
ン、メチルイソブチルケトン、シクロヘキサノン等、芳
香族系としてトルエン、キシレン等、ハロゲン系として
ジクロルメタン、トリクロロエタン等、ジオキサン、テ
トラヒドロフラン等およびこれらの混合物が挙げられる
。これらの溶剤は使用する色素を所定濃度以上に、かつ
バインダーを充分に溶解または分散するものとして選択
して使用することが重要である。例えば、色素とバイン
ダーとの合計重量の約5〜20倍の量の溶剤を使用する
のが好ましい。As the ink solvent for dissolving or dispersing the above-mentioned pigment and binder resin, conventionally known ink solvents can be freely used. Specifically, alcohol-based ink solvents include methanol, ethanol, isopropyl alcohol, butanol, isobutanol, etc. Examples of the ketone type include methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, etc.; aromatic types include toluene, xylene, etc.; halogen types include dichloromethane, trichloroethane, etc., dioxane, tetrahydrofuran, etc., and mixtures thereof. It is important to select and use these solvents in such a way that the dye used has a predetermined concentration or higher and the binder is sufficiently dissolved or dispersed. For example, it is preferred to use an amount of solvent that is about 5 to 20 times the combined weight of dye and binder.
熱転写色素供与材料の支持体としては従来公知のものが
いずれも使用できる0例えばポリエチレンテレフタレー
ト;ポリアミド;ポリカーボネート;グラシン祇;コン
デンサー祇;セルロースエステル;弗素ポリマー;ポリ
エーテル;ポリアセタール;ポリオレフィン;ポリイミ
ド;ポリマェフォン;セロファン等が挙げられる。As the support for the thermal transfer dye-providing material, any conventionally known support can be used.For example, polyethylene terephthalate; polyamide; polycarbonate; glassine; condenser; cellulose ester; fluorine polymer; polyether; polyacetal; polyolefin; polyimide; Examples include cellophane.
熱転写色素供与材料の支持体の厚みは、一般に2〜30
μである。必要に応じて下塗り層を付与してもよい。ま
た、親水性のポリマーよりなる色素の拡散防止層を支持
体と色素供与層の中間に設けてもよい。これによって転
写濃度が一層向上する。Il水性のポリマーとしては、
前記した水溶性ポリマーを用いることができる。The thickness of the support of the thermal transfer dye-providing material is generally 2 to 30 mm.
μ. An undercoat layer may be provided if necessary. Further, a dye diffusion preventing layer made of a hydrophilic polymer may be provided between the support and the dye-donating layer. This further improves the transfer density. As an Il aqueous polymer,
The water-soluble polymers described above can be used.
また、サーマルヘッドが色素供与材料に粘着するのを防
止するためにスワンピング層を設けてもよい、このスリ
ッピング層はポリマーバインダーを含有したあるいは含
有しない潤滑物質、例えば界面活性剤、固体あるいは液
体潤滑剤またはこれらの混合物から構成される。A swamping layer may also be provided to prevent the thermal head from sticking to the dye-donor material; this slipping layer may contain a lubricating material, such as a surfactant, solid or liquid, with or without a polymeric binder. Consists of lubricants or mixtures thereof.
本発明では上記のような色素供与層に加えて従来公知の
熱移行性色素を用いた色素供与層を同一支持体上に設け
てもよい。In the present invention, in addition to the dye-donating layer as described above, a dye-donating layer using a conventionally known heat-transferable dye may be provided on the same support.
具体的には、例えば分散染料、塩基性染料、油溶性染料
などが挙げられる。Specific examples include disperse dyes, basic dyes, and oil-soluble dyes.
色素供与材料には背面より印字するときにサーマルヘッ
ドの熱によるスティッキングを防止し、滑りをよくする
意味で、支持体の色素供与層を設けない側にスティッキ
ング防止処理を施すのがよい。In order to prevent sticking due to the heat of the thermal head and improve slippage when printing from the back side of the dye-donating material, it is preferable to apply an anti-sticking treatment to the side of the support on which the dye-donating layer is not provided.
例えば、■ポリビニルブチラール樹脂とイソシアネート
との反応生成物、■リン酸エステルのアルカリ金属塩ま
たはアルカリ土類金属塩、および■充填剤を主体とする
耐熱スリップ層を設けるのがよい、ポリビニルブチラー
ル樹脂としては分子量が6万〜20万程度で、ガラス転
移点が80〜110’Cであるもの、またイソシアネー
トとの反応サイトが多い観点からビニルブチラール部分
の重量%力月5〜40%のものがよい、リン酸エステル
のアルカリ金属塩またはアルカリ土類金属塩としては東
邦化学製のガファックRD720などが用いられ、ポリ
ビニルブチラール樹脂に対して1〜50重量%、好まし
くは10〜40重量%程重量いるとよい。For example, as a polyvinyl butyral resin, it is preferable to provide a heat-resistant slip layer mainly consisting of ■ a reaction product of polyvinyl butyral resin and an isocyanate, ■ an alkali metal salt or alkaline earth metal salt of a phosphoric acid ester, and ■ a filler. It is preferable to have a molecular weight of about 60,000 to 200,000, a glass transition point of 80 to 110'C, and a vinyl butyral moiety with a weight percentage of 5 to 40% from the viewpoint of having many reaction sites with isocyanate. As the alkali metal salt or alkaline earth metal salt of phosphoric acid ester, Gafac RD720 manufactured by Toho Chemical Co., Ltd. is used, and the amount is about 1 to 50% by weight, preferably 10 to 40% by weight based on the polyvinyl butyral resin. good.
耐熱スリップ層は下層に耐熱性を伴うことが望ましく、
加熱により硬化しうる合成樹脂とその硬化剤の組合せ、
例えばポリビニルブチラールと多価イソシアネート、ア
クリルポリオールと多価イソシアネート、酢酸セルロー
スとチタンキレート剤、もしくはポリエステルと有機チ
タン化合物などの組合せを塗布により設けるとよい。It is desirable that the heat-resistant slip layer has heat resistance as the lower layer.
A combination of a synthetic resin that can be cured by heating and its curing agent,
For example, a combination of polyvinyl butyral and polyvalent isocyanate, acrylic polyol and polyvalent isocyanate, cellulose acetate and a titanium chelating agent, or polyester and an organic titanium compound may be provided by coating.
色素供与材料には色素の支持体方向への拡散を防止する
ための親水性バリヤー層を設けることもある。親水性の
色素バリヤー層は、意図する目的に有用な親水性物質を
含んでいる。一般に優れた結果がゼラチン、ポリ(アク
リルアミド)、ポリ(イソプロピルアクリルアミド)、
メタクリル酸ブチルグラフトゼラチン、メタクリル酸エ
ヂルグラフトゼラチン、モノ酢酸セルロース、メチルセ
ルロース、ポリ(ビニルアルコール)、ポリ(エチレン
イミン)、ポリ(アクリル酸)、ポリ(ビニルアルコー
ル)とポリ(酢酸ビニル)との混合物、ポリ(ビニルア
ルコール)とポリ(アクリル酸)との混合物またはモノ
酢酸セルロースとポリ(アクリル酸)との混合物を用い
ることによって得られる。特に好ましいものは、ポリ(
アクリル酸)、モノ酢6セルロースまたはポリ(ビニル
アルコール)である。The dye-donor element may also be provided with a hydrophilic barrier layer to prevent diffusion of the dye towards the support. Hydrophilic dye barrier layers contain hydrophilic materials useful for their intended purpose. Generally excellent results are obtained with gelatin, poly(acrylamide), poly(isopropylacrylamide),
Butyl methacrylate grafted gelatin, edyl methacrylate grafted gelatin, cellulose monoacetate, methylcellulose, poly(vinyl alcohol), poly(ethyleneimine), poly(acrylic acid), poly(vinyl alcohol) and poly(vinyl acetate) It is obtained by using a mixture, a mixture of poly(vinyl alcohol) and poly(acrylic acid) or a mixture of cellulose monoacetate and poly(acrylic acid). Particularly preferred is poly(
acrylic acid), monoacetic acid 6 cellulose or poly(vinyl alcohol).
色素供与材料には下塗り層を設けてもよい。本発明では
所望の作用をすればどのような下塗り層でもよいが、好
ましい具体例としては、(アクリロニトリル−塩化ビニ
リデン−アクリル酸)共重合体(重量比14:80:6
)、(アクリル酸ブチル−メタクリル酸−2−アミノエ
チル−メタクリル酸−2−ヒドロキシエチル)共重合体
(重量比30:20:50)、線状/飽和ポリエステル
例えばボスティック7650 (エムハート社、ボステ
ィック・ケミカル・グループ)または塩素化高密度ポリ
(エチレン−トリクロロエチレン)樹脂が挙げられる。The dye-providing material may be provided with a subbing layer. In the present invention, any undercoat layer may be used as long as it has the desired effect, but a preferred specific example is (acrylonitrile-vinylidene chloride-acrylic acid) copolymer (weight ratio 14:80:6).
), (butyl acrylate-2-aminoethyl methacrylate-2-hydroxyethyl methacrylate) copolymer (weight ratio 30:20:50), linear/saturated polyester such as Bostik 7650 (Emhart, Bostic) stick chemical group) or chlorinated high density poly(ethylene-trichloroethylene) resins.
下塗り層の塗布量には特別な制限はないが、通常0.1
〜2.0g/m”の量で用いられる。There is no particular limit to the amount of undercoat layer applied, but it is usually 0.1
~2.0 g/m'' is used.
(以下余白)
熱転写記録方法を実施する上において本発明の熱転写色
素供与材料と共に用いられる熱転写受像材料について説
明する。この熱転写受像材料は支持体の上に少なくとも
1層の熱移行性色素を受容しうる受像層を設けたもので
ある。(The following is a blank space) The thermal transfer image-receiving material used together with the thermal transfer dye-providing material of the present invention in carrying out the thermal transfer recording method will be described. This thermal transfer image-receiving material has an image-receiving layer capable of receiving at least one heat-transferable dye on a support.
本発明の熱転写受像材料に用いる支持体は転写温度に耐
えることができ、平滑性、白色度、滑り性、摩擦性、帯
電防止性、転写後のへこみなどの点で要求を満足できる
ものならばどのようなものでも使用できる。例えば、合
成紙(ポリオレフィン系、ポリスチレン系などの合成紙
)、上質紙、アート紙、コート紙、キャストコート紙、
壁紙、裏打用紙、合成樹脂またはエマルジョン含浸紙、
合成ゴムラテックス含浸紙、合成樹脂内添紙、板紙、セ
ルロース繊維紙、ポリオレフィンコート紙(特にポリエ
チレンで両側を被覆したMl)などの紙支持体、ポリオ
レフィン、ポリ塩化ビニル、ポリエチレンテレフタレー
ト、ポリスチレン、メタクリレート、ポリカーボネート
等の各種のプラスチックフィルムまたはシートとこのプ
ラスチックに白色反射性を与える処理をしたフィルムま
たはシート、また上記の任意の組合せによる積層体も使
用できる。The support used in the thermal transfer image-receiving material of the present invention can withstand the transfer temperature and satisfies the requirements in terms of smoothness, whiteness, slipperiness, friction, antistatic property, denting after transfer, etc. You can use anything. For example, synthetic paper (polyolefin-based, polystyrene-based, etc.), high-quality paper, art paper, coated paper, cast coated paper,
wallpaper, lined paper, synthetic resin or emulsion impregnated paper,
Paper supports such as synthetic rubber latex impregnated paper, synthetic resin internalized paper, paperboard, cellulose fiber paper, polyolefin coated paper (especially Ml coated on both sides with polyethylene), polyolefin, polyvinyl chloride, polyethylene terephthalate, polystyrene, methacrylate, Various plastic films or sheets such as polycarbonate, films or sheets treated to impart white reflective properties to the plastic, and laminates made of any combination of the above may also be used.
この中でもポリオレフィンコート紙は熱転写時の加熱に
よる凹状の変形を起こさないこと、白色度に優れること
、カールが少ないことなどの特長を有しているので好ま
しい。Among these, polyolefin coated paper is preferred because it has features such as not causing concave deformation due to heating during thermal transfer, excellent whiteness, and little curling.
熱転写受像材料には色素の受像層が設けられる。The thermal transfer image-receiving material is provided with a dye image-receiving layer.
この受像層は、印字の際に熱転写色素供与材料から移行
してくる熱移行性色素を受は入れ、熱移行性色素が染着
する働きを有している色素受容性物質を単独で、または
その他のバインダー物質とともに含んでいる厚み0.
5〜50μ層程度の被膜であることが好ましい。This image-receiving layer receives the heat-transferable dye transferred from the thermal transfer dye-providing material during printing, and contains a dye-receiving substance that functions to dye the heat-transferable dye alone or Thickness 0.0, including with other binder materials.
It is preferable that the film has a thickness of about 5 to 50 μm.
色素受容性物質の代表例である色素受容性ポリマーとし
ては次のような樹脂が挙げられる。Examples of dye-receiving polymers that are representative examples of dye-receiving substances include the following resins.
(イ)エステル結合を有するもの
テレフタル酸、イソフタル酸、コハク酸などのジカルボ
ン酸成分(これらのジカルボン酸成分にはスルホン基、
カルボキシル基などが置換していてもよい)と、エチレ
ングリコール、ジエチレングリコール、プロピレングリ
コール、ネオペンチルグリコール、ビスフェノールAな
どの縮合により得られるポリエステル樹脂:ポリメチル
メタクリレート、ポリブチルメタクリレート、ポリメチ
ルアクリレート、ポリブチルアクリレートなどのポリア
クリル酸エステル樹脂またはポリメタクリル酸エステル
樹脂:ボリカーボネート樹脂:ポリ酢酸ビニル樹脂:ス
チレンアクリレート樹脂:ビニルトルエンアクリレート
樹脂など。具体的には特開昭59−101395号、同
63−7971号、同63−7972号、同63−79
73号、同60−294862号、に記載のものを挙げ
ることができる。また、市販品としては東洋紡製のバイ
ロン290.バイロン2001バイロン280、バイロ
ン300、バイロン103、バイロンGK−140、バ
イロンGK−130、花王製のATR−2009、AT
R−2010などが使用できる。(a) Dicarboxylic acid components having ester bonds such as terephthalic acid, isophthalic acid, and succinic acid (these dicarboxylic acid components contain sulfonic groups,
Polyester resins obtained by condensation of ethylene glycol, diethylene glycol, propylene glycol, neopentyl glycol, bisphenol A, etc. with carboxyl groups (which may be substituted with carboxyl groups, etc.): polymethyl methacrylate, polybutyl methacrylate, polymethyl acrylate, polybutyl Polyacrylic acid ester resin or polymethacrylic acid ester resin such as acrylate: Polycarbonate resin: Polyvinyl acetate resin: Styrene acrylate resin: Vinyl toluene acrylate resin, etc. Specifically, JP-A No. 59-101395, No. 63-7971, No. 63-7972, and No. 63-79.
Examples include those described in No. 73 and No. 60-294862. In addition, as a commercially available product, Byron 290 manufactured by Toyobo. Byron 2001 Byron 280, Byron 300, Byron 103, Byron GK-140, Byron GK-130, Kao ATR-2009, AT
R-2010 etc. can be used.
口)ウレタン結合を有するもの ポリウレタン樹脂など。Mouth) Those with urethane bond polyurethane resin, etc.
(ハ)アミド結合を有するもの ポリアミド樹脂など。(c) Those with an amide bond polyamide resin, etc.
(ニ)尿素結合を有するもの 尿素樹脂など。(d) Those with urea bonds urea resin etc.
(ホ)スルホン結合を有するもの。(e) Those with a sulfone bond.
ポリスルホン樹脂など。polysulfone resin, etc.
(へ)その他極性の高い結合を有するものポリカプロラ
クトン樹脂、スチレン−無水マレイン酸樹脂、ポリ塩化
ビニル樹脂、ポリアクリロニトリル樹脂など。(f) Others having highly polar bonds, such as polycaprolactone resin, styrene-maleic anhydride resin, polyvinyl chloride resin, polyacrylonitrile resin, etc.
上記のような合成樹脂に加えて、これらの混合物あるい
は共重合体なども使用できる。In addition to the synthetic resins mentioned above, mixtures or copolymers thereof can also be used.
熱転写受像材料中、特に受像層中には、色素受容性物質
として、または色素の拡散助剤として高沸点有機溶剤ま
たは熱溶剤を含有させることができる。The thermal transfer image-receiving material, particularly the image-receiving layer, may contain a high-boiling organic solvent or a thermal solvent as a dye-receiving substance or as a dye diffusion aid.
高沸点有機溶剤および熱溶剤の具体例としては特開昭6
2−174754号、同62−245253号、同61
−209444号、同61−200538号、同62−
8145号、同62−9348号、同62−30247
号、同62−136646号に記載の化合物を挙げるこ
とができる。Specific examples of high boiling point organic solvents and thermal solvents include JP-A No. 6
No. 2-174754, No. 62-245253, No. 61
-209444, 61-200538, 62-
No. 8145, No. 62-9348, No. 62-30247
No. 62-136646.
本発明の熱転写受像材料の受像層は、色素受容性物質を
水溶性バインダーに分散して担持する構成としてもよい
、この場合に用いられる水溶性バインダーとしては公知
の種々の水溶性ポリマーを使用しうるが、硬膜剤により
架橋反応しうる基を有する水溶性のポリマーが好ましく
、中でもゼラチン類が特に好ましい。The image-receiving layer of the thermal transfer image-receiving material of the present invention may have a structure in which the dye-receiving substance is dispersed and supported in a water-soluble binder. In this case, various known water-soluble polymers may be used as the water-soluble binder. However, water-soluble polymers having a group capable of crosslinking with a hardening agent are preferred, and among them, gelatins are particularly preferred.
色素受容性物質を水溶性バインダー中に分散する方法と
しては、疎水性物質を水溶性ポリマーに分散する際の公
知の分散方法のいずれもが使用できる。代表的には、色
素受容性物質を水と非混和性の有機溶剤に溶解した液を
水溶性バインダーの水溶液と混合して乳化分散する方法
、色素受容性物質(ポリマー)のラテックスを水溶性バ
インダーの水溶液と混合する方法などがある。As a method for dispersing the dye-receiving substance in the water-soluble binder, any known dispersion method for dispersing a hydrophobic substance in a water-soluble polymer can be used. Typical methods include emulsifying and dispersing a dye-receiving substance dissolved in an organic solvent that is immiscible with water and mixing it with an aqueous solution of a water-soluble binder; There are methods such as mixing with an aqueous solution of
受像層は1層でもよいし、2層以上の層で構成してもよ
い、2層以上設ける場合、支持体に近い方の層にはガラ
ス転位点の低い合成樹脂を用いたり、高沸点有機溶剤や
熱溶剤を用いて色素に対する染着性を高めた構成にし、
最外層にはガラス転位点のより高い合成樹脂を用いたり
、高沸点有機溶剤や熱溶剤の使用量を必要最小限にする
かもしくは使用しないで表面のベタツキ、他の物質との
接着、転写後の色素の他物質への再転写、熱転写色素供
与材料とのブロッキング等の故障を防止する構成にする
ことが望ましい。The image-receiving layer may be composed of one layer or two or more layers. If two or more layers are provided, the layer closer to the support may be made of a synthetic resin with a low glass transition point or a high-boiling point organic resin. The structure uses solvents and hot solvents to improve the dyeability of dyes,
For the outermost layer, use a synthetic resin with a higher glass transition point, minimize the amount of high-boiling point organic solvents and hot solvents, or avoid using them to prevent surface stickiness, adhesion with other substances, and post-transfer. It is desirable to have a structure that prevents failures such as re-transfer of the dye to other substances and blocking with the thermal transfer dye-providing material.
受像層の厚さは全体で0.5〜50μm、特に3〜30
μm、2層構成の場合、最外層は0.1〜2μm、特に
0.2〜1μmの範囲にするのが好ましい。The total thickness of the image-receiving layer is 0.5 to 50 μm, particularly 3 to 30 μm.
In the case of a two-layer structure, the outermost layer preferably has a thickness of 0.1 to 2 μm, particularly 0.2 to 1 μm.
本発明の熱転写受像材料は、支持体と受像層の間に中間
層を存してもよい。The thermal transfer image-receiving material of the present invention may have an intermediate layer between the support and the image-receiving layer.
中間層は構成する材質により、クツション層、多孔層、
色素の拡散防止層のいずれか又はこれらの2つ以上の機
能を備えた層であり、場合によっては接着剤の役目も兼
ねている。The intermediate layer can be a cushion layer, a porous layer, or a
This layer has one of the functions of a dye diffusion prevention layer or a layer having two or more of these functions, and in some cases also serves as an adhesive.
色素の拡散防止層は、特に熱移行性色素が支持体に拡散
するのを防止する役目を果たすものである。この拡散防
止層を構成するバインダーとしては、水溶性でも有機溶
剤可溶性でもよいが、水溶性のバインダーが好ましく、
その例としては前述の受像層のバインダーとして挙げた
水溶性バインダー、特にゼラチンが好ましい。The dye diffusion-preventing layer plays a role, in particular, in preventing the heat-transferable dye from diffusing into the support. The binder constituting this diffusion prevention layer may be water-soluble or organic solvent-soluble, but preferably a water-soluble binder.
Preferred examples include the water-soluble binders mentioned above as binders for the image-receiving layer, particularly gelatin.
多孔層は、熱転写時に印加した熱が受像層から支持体へ
拡散するのを防止し、印加された熱を有効に利用する役
目を果たす層である。The porous layer is a layer that prevents the heat applied during thermal transfer from diffusing from the image-receiving layer to the support and effectively utilizes the applied heat.
本発明の熱転写受像材料を構成する受像層、クツション
層、多孔層、拡散防止層、接着層等には、シリカ、クレ
ー、タルク、ケイソウ土、炭酸カルシウム、硫酸カルシ
ウム、硫酸バリウム、ケイ酸アルミニウム、合成ゼオラ
イト、酸化亜鉛、リトポン、酸化チタン、アルミナ等の
微粉末を含有させてもよい。The image receiving layer, cushion layer, porous layer, diffusion prevention layer, adhesive layer, etc. constituting the thermal transfer image receiving material of the present invention include silica, clay, talc, diatomaceous earth, calcium carbonate, calcium sulfate, barium sulfate, aluminum silicate, Fine powders of synthetic zeolite, zinc oxide, lithopone, titanium oxide, alumina, etc. may also be included.
熱転写受像材料には蛍光増白剤を用いてもよい。A fluorescent brightener may be used in the thermal transfer image-receiving material.
その例としては、K、Veenkataraman[r
The Cheststry of 5yntheti
c DyesJ第 巻第8章、特開昭61−14375
2号などに記載されている化合物を挙げることができる
。より具体的には、スチルベン系化合物、クマリン系化
合物、ビフェニル系化合物、ベンゾオキサシリル系化合
物、ナフタルイミド系化合物、ピラゾリン系化合物、カ
ルボスチリル系化合物、2.5−ジベンゾオキサゾール
チオフェン系化合物などが挙げられる。Examples include K, Veenkataraman[r
The Chesttry of 5yntheti
c DyesJ Volume 8 Chapter 8, JP-A-61-14375
Examples include compounds described in No. 2 and the like. More specifically, stilbene compounds, coumarin compounds, biphenyl compounds, benzoxacylyl compounds, naphthalimide compounds, pyrazoline compounds, carbostyril compounds, 2,5-dibenzoxazolethiophene compounds, etc. It will be done.
蛍光増白剤は退色防止剤と組み合わせて用いることがで
きる。Optical brighteners can be used in combination with antifade agents.
本発明において、熱転写色素供与材料と熱転写受像材料
との離型性を向上させるために、色素供与材料および/
または受像材料を構成する層中、特に好ましくは両方の
材料が接触する面に当たる最外層に離型剤を含有させる
のが好ましい。In the present invention, in order to improve the releasability of the thermal transfer dye-providing material and the thermal transfer image-receiving material, the dye-providing material and/or
Alternatively, it is preferable to include a release agent in the layers constituting the image-receiving material, particularly preferably in the outermost layer corresponding to the surface where both materials come into contact.
離型剤としては、ポリエチレンワックス、アミドワック
ス、テフロンパウダー等の固形あるいはワックス状物質
:弗素系、リン酸エステル系等の界面活性剤:パラフィ
ン系、シリコーン系、弗素系のオイル類等、従来公知の
離型剤がいずれも使用できるが、特にシリコーンオイル
が好ましい。Examples of mold release agents include solid or waxy substances such as polyethylene wax, amide wax, and Teflon powder; surfactants such as fluorine-based and phosphate esters; and conventionally known oils such as paraffin-based, silicone-based, and fluorine-based oils. Although any of the above mold release agents can be used, silicone oil is particularly preferred.
シリコーンオイルとしては、無変性のもの以外にカルボ
キシ変性、アミノ変性、エポキシ変性等の変性シリコー
ンオイルを用いることができる。As the silicone oil, in addition to unmodified silicone oil, modified silicone oils such as carboxy-modified, amino-modified, and epoxy-modified silicone oils can be used.
その例としては、信越シリコーン(株)発行の[変性シ
リコーンオイル」技術資料の6〜18B頁に記載の各種
変性シリコーンオイルを挙げることができる。有Ja溶
剤系のバインダー中に用いる場合は、このバインダーの
架橋剤と反応しうる基(例えばイソシアネートと反応し
うる基)を有するアミノ変性シリコーンオイルが、また
水溶性バインダー中に乳化分散して用いる場合は、カル
ボキシ変性シリコーンオイル(例えば信越シリコーン(
株)製:商品名X−22−3710)が有効である。Examples include various modified silicone oils described on pages 6 to 18B of the "Modified Silicone Oil" technical data published by Shin-Etsu Silicone Co., Ltd. When used in a Ja-containing solvent-based binder, an amino-modified silicone oil having a group that can react with the crosslinking agent of the binder (for example, a group that can react with isocyanate) is also emulsified and dispersed in a water-soluble binder. If so, use carboxy-modified silicone oil (for example, Shin-Etsu silicone (
Co., Ltd. (trade name: X-22-3710) is effective.
熱転写色素供与材料や熱転写受像材料には退色防止剤を
用いてもよい。退色防止剤としては、例えば酸化防止剤
、紫外線吸収剤、あるいはある種の金属錯体がある。熱
転写色素供与材料に退色防止剤を用いる場合は、色素供
与層に含ませてもよいし、また支持体上の色素供与層を
設けた領域とは別の領域に設けてもよい。Antifading agents may be used in the thermal transfer dye-providing material and the thermal transfer image-receiving material. Antifading agents include, for example, antioxidants, ultraviolet absorbers, or certain metal complexes. When an antifading agent is used in the thermal transfer dye-providing material, it may be included in the dye-providing layer, or it may be provided in an area on the support separate from the area in which the dye-providing layer is provided.
酸化防止剤としては、例えばクロマン系化合物、クマラ
ン系化合物、フェノール系化合物(例えばヒンダードフ
ェノールN)、ハイドロキノン誘導体、ヒンダードアミ
ン誘導体、スピロインダン系化合物がある。また、特開
昭61−159644号記載の化合物も有効である。Examples of antioxidants include chroman compounds, coumaran compounds, phenol compounds (for example, hindered phenol N), hydroquinone derivatives, hindered amine derivatives, and spiroindane compounds. Compounds described in JP-A-61-159644 are also effective.
紫外線吸収剤としては、ベンゾトリアゾール系化合物(
米国特許第3.533.794号など)、4−チアゾリ
ドン系化合物(米国特許第3.352681号など)、
ベンゾフェノン系化合物(特開昭56−2784号など
)、その他特開昭54=48535号、同62−136
641号、同61−88256号等に記載の化合物があ
る。また、特開昭62−260152号記載の紫外線吸
収性ポリマーも有効である。Benzotriazole compounds (
U.S. Patent No. 3.533.794, etc.), 4-thiazolidone compounds (U.S. Pat. No. 3.352681, etc.),
Benzophenone compounds (JP-A No. 56-2784, etc.), other JP-A-54 No. 48535, JP-A No. 62-136
There are compounds described in No. 641, No. 61-88256, and the like. Further, the ultraviolet absorbing polymer described in JP-A No. 62-260152 is also effective.
金属錯体としては、米国特許第4.241,155号、
同第4.245.018号第3〜36欄、同第4.25
4,195号第3〜8欄、特開昭62−174741号
、同61−88256号(27)〜(29)頁、特願昭
62−234103号、同62−31096号、特願昭
62−230596号等に記載されている化合物がある
。As metal complexes, U.S. Pat. No. 4,241,155;
No. 4.245.018, columns 3 to 36, No. 4.25 of the same
No. 4,195, columns 3 to 8, JP-A-62-174741, JP-A-61-88256, pages (27)-(29), Japanese Patent Application No. 1983-234103, JP-A No. 62-31096, Japanese Patent Application No. 1983 There are compounds described in No.-230596 and the like.
有用な退色防止剤の例は特開昭62−215272号(
125)〜(137)頁に記載されている。Examples of useful anti-fading agents are disclosed in JP-A No. 62-215272 (
125) to (137).
受像材料に転写された色素の退色を防止するための退色
防止剤は予め受像材料に含有させておいてもよいし、色
素供与材料から転写させるなどの方法で外部から受像材
料に供給するようにしてもよい。The anti-fading agent for preventing fading of the dye transferred to the image-receiving material may be included in the image-receiving material in advance, or it may be supplied to the image-receiving material from the outside by a method such as transfer from a dye-donating material. You can.
上記の酸化防止剤、紫外線吸収剤、金属錯体はこれら同
士を組み合わせて使用してもよい。The above antioxidants, ultraviolet absorbers, and metal complexes may be used in combination.
本発明に用いる熱転写色素供与材料および熱転写受像材
料を構成する層は硬膜剤によって硬化されていてもよい
。The layers constituting the thermal transfer dye-providing material and the thermal transfer image-receiving material used in the present invention may be hardened with a hardening agent.
有機溶剤系のポリマーを硬化する場合には、特開昭61
−199997号、同5B−215398号等に記載さ
れている硬膜剤が使用できる。ポリエステル樹脂に対し
ては特にイソシアネート系の硬膜剤の使用が好ましい。When curing organic solvent-based polymers, JP-A-61
Hardeners described in Japanese Patent No. 199997 and No. 5B-215398 can be used. For polyester resins, it is particularly preferable to use isocyanate-based hardeners.
水溶性ポリマーの硬化には、米国特許第4.678.7
39号第41欄、特開昭59−116655号、同62
−245261号、同61−18942号等に記載の硬
膜剤が使用に適している。For curing water-soluble polymers, U.S. Patent No. 4.678.7
No. 39, column 41, JP-A-59-116655, JP-A No. 62
Hardeners described in Japanese Patent Nos. 245261 and 61-18942 are suitable for use.
より具体的には、アルデヒド系硬膜剤(ホルムアルデヒ
ドなど)、アジリジン系硬膜剤、エポキシ系硬膜剤
ビス(ビニルスルホニルアセタミド)エタンなど)、N
−メチロール系硬膜剤(ジメチロール尿素など)、ある
いは高分子硬膜剤(特開昭62−234157号などに
記載の化合物)が挙げられる。More specifically, aldehyde hardeners (formaldehyde, etc.), aziridine hardeners, epoxy hardeners (bis(vinylsulfonylacetamide)ethane, etc.), N
-Methylol hardeners (dimethylol urea, etc.) or polymer hardeners (compounds described in JP-A-62-234157, etc.).
熱転写受像材料には予め前述したような退色防止剤を含
有させておいてもよい。The thermal transfer image-receiving material may contain a fading inhibitor as described above in advance.
熱転写色素供与材料や熱転写受像材料の構成層には塗布
助剤、剥離性改良、スベリ性改良、帯電防止、現像促進
等の目的で種々の界面活性剤を使用することができる。Various surfactants can be used in the constituent layers of the thermal transfer dye-providing material and the thermal transfer image-receiving material for the purposes of coating aids, improving peelability, improving slipperiness, preventing electrification, accelerating development, and the like.
非イオン性界面活性剤、アニオン界面活性剤。Nonionic surfactants, anionic surfactants.
両性界面活性剤、カチオン界面活性剤を用いることがで
きる。これらの具体例は特開昭62−173463号、
同62−183457号等に記載されている。Amphoteric surfactants and cationic surfactants can be used. Specific examples of these are JP-A-62-173463,
It is described in No. 62-183457 and the like.
また、熱移行性色素を受容しうる物質、離型剤、退色防
止剤、紫外線吸収剤、蛍光増白剤その他の疎水性化合物
を水溶性バインダー中に分散する際には、分散助剤とし
て界面活性剤を用いるのが好ましい、この目的のために
は、上記の界面活性剤の他に、特開昭59−15763
6号の37〜38頁に記載の界面活性剤が特に好ましく
用いられる。In addition, when dispersing substances that can accept heat-transferable dyes, mold release agents, anti-fading agents, ultraviolet absorbers, optical brighteners, and other hydrophobic compounds in a water-soluble binder, the interface is used as a dispersion aid. It is preferable to use surfactants; for this purpose, in addition to the above-mentioned surfactants, JP-A-59-15763
The surfactants described on pages 37-38 of No. 6 are particularly preferably used.
熱転写色素供与材料や熱転写受像材料の構成層には、ス
ベリ性改良、帯電防止、剥離性改良等の目的で有機フル
オロ化合物を含ませてもよい、有機フルオロ化合物の代
表例としては、特公昭57−9053号第8〜1711
4.特開昭61−20944号、同62−135826
号等に記載されているフッ素系界面活性剤、またはフッ
素油などのオイル状フッ素系化合物もしくは四フッ化エ
チレン樹脂などの固体状フッ素化合物樹脂などの疎水性
フッ素化合物が挙げられる。The constituent layers of the thermal transfer dye-providing material and the thermal transfer image-receiving material may contain an organic fluoro compound for the purpose of improving slipperiness, preventing static electricity, improving releasability, etc. Representative examples of organic fluoro compounds include Japanese Patent Publication No. 57 -9053 No. 8 to 1711
4. JP-A-61-20944, JP-A No. 62-135826
Hydrophobic fluorine compounds such as oily fluorine compounds such as fluorine oil, or solid fluorine compound resins such as tetrafluoroethylene resin are mentioned.
熱転写色素供与材料や熱転写受像材料にはマット剤を用
いることができる。マット剤としては二酸化ケイ素、ポ
リオレフィンまたはポリメタクリレートなどの特開昭6
1−88256号(29)頁記載の化合物の他に、ベン
ゾグアナミン樹脂ビーズ、ポリカーボネート樹脂ビーズ
、AS樹脂ビーズなどの特願昭62−110064号、
同62−110065号記載の化合物がある。A matting agent can be used in the thermal transfer dye-providing material and the thermal transfer image-receiving material. As a matting agent, silicon dioxide, polyolefin, polymethacrylate, etc.
In addition to the compounds described on page 29 of No. 1-88256, Japanese Patent Application No. 110064/1988, such as benzoguanamine resin beads, polycarbonate resin beads, and AS resin beads,
There is a compound described in No. 62-110065.
本発明においては、熱転写色素供与材料を熱転写受像材
料と重ね合わせ、いずれかの面から、好ましくは熱転写
色素供与材料の裏面から、例えばサーマルヘッド等の加
熱手段により画像情報に応じた熱エネルギーを与えるこ
とにより、色素供与層の色素を熱転写受像材料に加熱エ
ネルギーの大小に応じて転写することができ、優れた鮮
明性、解像性の階調のあるカラー画像を得ることができ
る。また、退色防止剤も同様にして転写できる。In the present invention, a thermal transfer dye-providing material is superimposed on a thermal transfer image-receiving material, and thermal energy is applied according to image information from either side, preferably from the back side of the thermal transfer dye-providing material, using a heating means such as a thermal head. Thereby, the dye in the dye-donating layer can be transferred to the thermal transfer image-receiving material depending on the magnitude of heating energy, and a color image with excellent clarity and resolution and gradation can be obtained. Further, the anti-fading agent can also be transferred in the same manner.
加熱手段はサーマルヘッドに限らず、レーザー光(例え
ば半導体レーザー)、赤外線フラッシュ、熱ペンなどの
公知のものが使用できる。The heating means is not limited to a thermal head, and known means such as a laser beam (for example, a semiconductor laser), an infrared flash, a thermal pen, etc. can be used.
本発明において、熱転写色素供与材料は熱転写受像材料
と組合せることにより、熱印字方式の各種プリンターを
用いた印字、ファクシミリ、あるいは磁気記録方式、光
磁気記録方式、光記録方式等による画像のプリント作成
、テレビジョン、CRT画面からのプリント作成等に利
用できる。In the present invention, by combining the thermal transfer dye-providing material with the thermal transfer image-receiving material, images can be printed by printing using various thermal printing printers, by facsimile, or by magnetic recording, magneto-optical recording, optical recording, etc. It can be used to create prints from , television, and CRT screens.
熱転写記録方法の詳細については、特開昭60−348
95号の記載を参照できる。For details on the thermal transfer recording method, see Japanese Patent Application Laid-Open No. 60-348.
You can refer to the description in No. 95.
(以下余白)
(実施例)
以下の実施例および比較例において熱転写色素供与材料
および熱転写受像材料の製造、両材料を用いた印字、熱
転写受像材料の試験は次のように行った。(Left below) (Example) In the following Examples and Comparative Examples, the production of a thermal transfer dye-providing material and a thermal transfer image-receiving material, printing using both materials, and testing of a thermal transfer image-receiving material were conducted as follows.
実施例1
(熱転写色素供与材料の作成)
支持体として裏面に耐熱滑性処理が施された厚み6μm
のポリエチレンテレフタレートフィルム(奇人製)を使
用し、フィルムの表面上に、表1に記載の色素を用い、
下記組成の熱転写色素供与層用塗料組成物をワイヤーバ
ーコーティングにより、乾燥時の厚みが1.5μmとな
るように塗布形成し、熱転写色素供与材料を作成した。Example 1 (Preparation of thermal transfer dye-providing material) A support with a thickness of 6 μm and whose back surface was subjected to heat-resistant slipping treatment.
using a polyethylene terephthalate film (manufactured by Kijin), using the dyes listed in Table 1 on the surface of the film,
A thermal transfer dye-providing material was prepared by applying a coating composition for a thermal transfer dye-providing layer having the following composition by wire bar coating to a dry thickness of 1.5 μm.
】
色素 xgポリビニル
ブチラール樹脂(電気化学
型 デンカブチラール500−A) ygトルエン
40ailメチルエチルケト
ン 40dポリイソシアネート(底円薬
品製
タケネー1−DIION) (0,10ym1)ポ
リマーの1/10噴
(熱転写受像材料の作成)
基材として厚み150μmの合成紙(玉子油化製、YU
PO−FP(、−150)を用い、表面に下記組成の受
像層用塗料組成物(1)をワイヤーバーコーティングに
より乾燥時の厚さが8)tmとなるように塗布して熱転
写受像材料(1)を形成した。乾燥はドライヤーで仮乾
燥後、温度100“Cのオーブン中で30分間行った。] Dye xg Polyvinyl butyral resin (electrochemical type Denka Butyral 500-A) yg Toluene
40ail methyl ethyl ketone 40d polyisocyanate (Takene 1-DIION manufactured by Sotoen Yakuhin) (0,10ym1) 1/10 injection of polymer (preparation of thermal transfer image receiving material) Synthetic paper with a thickness of 150 μm (made by Tamago Yuka, YU) as a base material
A thermal transfer image-receiving material (PO-FP, -150) was prepared by coating the surface of the image-receiving layer coating composition (1) with the following composition by wire bar coating to a dry thickness of 8) tm. 1) was formed. Drying was performed for 30 minutes in an oven at a temperature of 100"C after temporary drying with a hair dryer.
叉像l工塗料」衷紛但
ポリエステル樹脂(東洋紡製
バイロン−280) 22gポリイソ
シアネート(KP−
90:大日本インキ化学製) 4gアミノ変
性シリコーンオイル
(信越シリコーン製KF−857) 0.5gメチル
エチルケトン 85成トルエン
E15dメチルプロピレングリコー
ル
表1
5−
イエロー(2)
マゼンタ(4)
シアン(2)
m、 p、 185°C
m、 p、 179°C
上記のようにして得られた色素供与材料と受像材料とを
色素供与層と受像層とが接するように重ね合せ、色素供
与材料の支持体側から熱ヘツドを使用し、出力0.25
W/ドツト、パルス巾0゜15〜15m5ec、ドツト
密度6ドソト/1nfflの条件で熱転写を行ない、受
像材料に像状の記録画像を得た。Polyester resin (Vylon-280 manufactured by Toyobo Co., Ltd.) 22 g Polyisocyanate (KP-90: manufactured by Dainippon Ink Chemical Co., Ltd.) 4 g Amino-modified silicone oil (KF-857 manufactured by Shin-Etsu Silicone Co., Ltd.) 0.5 g Methyl ethyl ketone 85 Synthetic toluene
E15d Methylpropylene glycol Table 1 5- Yellow (2) Magenta (4) Cyan (2) m, p, 185°C m, p, 179°C The dye-donating material and image-receiving material obtained as above were combined. The dye-providing layer and image-receiving layer are stacked so that they are in contact with each other, and a thermal head is used from the support side of the dye-providing material to give an output of 0.25.
Thermal transfer was carried out under the conditions of W/dot, pulse width of 0°15 to 15 m5 ec, and dot density of 6 dots/1 ffl to obtain a recorded image on the image-receiving material.
得られた記録画像を本発明の場合と比較例とを表−2に
示す。またこれらの色素供与材料を50゛Cの条件に1
4日間設置した後の色素の析出を顕微鏡で調べた。結果
を表2に示す。Table 2 shows the recorded images obtained in the case of the present invention and in the comparative example. In addition, these dye-providing materials were heated at 50°C for 1
The precipitation of the dye after being placed for 4 days was examined using a microscope. The results are shown in Table 2.
この結果より本発明の色素供与材料は比較例に比し最大
転写濃度が高く、又低エネルギーでの転写濃度も高い。These results show that the dye-providing material of the present invention has a higher maximum transfer density than the comparative example, and also has a higher transfer density at low energy.
また、長期保存時の色素の析出も認められなかった。Further, no precipitation of dye was observed during long-term storage.
実施例2
実施例−1の熱転写色素供与層塗料組成物のポリビニル
ブチラール樹脂に変えて、表−3に示した樹脂を用いて
熱転写色素供与材料を作成した。Example 2 A thermal transfer dye-providing material was prepared using the resin shown in Table 3 instead of the polyvinyl butyral resin in the thermal transfer dye-providing layer coating composition of Example-1.
実施例1と同様の受像材料を用いて熱転写を行ったとこ
ろ、高濃度の画像記録が得られた。また色素供与材料の
保存性も優れていた。When thermal transfer was performed using the same image-receiving material as in Example 1, a high-density image recording was obtained. Furthermore, the storage stability of the dye-providing material was also excellent.
表3
実施例−3
(熱転写受像材料(2)の作製)
200μの紙の両面にそれぞれ15μ、25μの厚みに
ポリエチレンをラミネートしたレジンコート紙を用意し
、15μ厚みのラミネートされた面に下記組成の受像層
用塗料組成物をワイヤーバーコーティングで乾燥厚みl
Oμになるように塗布し、乾燥して熱転写受像材料(2
)を作製した。Table 3 Example-3 (Preparation of thermal transfer image-receiving material (2)) Resin-coated paper was prepared by laminating polyethylene to a thickness of 15μ and 25μ on both sides of a 200μ paper, and the following composition was applied to the 15μ thick laminated side. The paint composition for the image-receiving layer is coated with a wire bar to a dry thickness of l.
Coat it so that it has a thickness of Oμ, and dry it to form a thermal transfer image-receiving material (2
) was created.
受像層用塗料組成物
ポリエステル樹脂NαI 25gアミ
ン変性シリコーンオイル
(KF857:信越シリコーン製)0.8gポリイソシ
アネート
(KP−90:大日本インキ製) 4gメチ
ルエチルケトン 10〇−トルエン
10〇−エポキシ変性シリコー
ンオイル
(KF−100T:信越シリコーン製)0.5g
メチルエチルケトン 85dトルエン
85−シクロへキサノン
301i!実施例−1と同様に
して熱転写したところ、転写濃度の高い画像記録が得ら
れた。Coating composition for image-receiving layer Polyester resin NαI 25g Amine-modified silicone oil (KF857: manufactured by Shin-Etsu Silicone) 0.8g Polyisocyanate (KP-90: manufactured by Dainippon Ink) 4g Methyl ethyl ketone 100-Toluene
100-Epoxy modified silicone oil (KF-100T: Shin-Etsu Silicone) 0.5g Methyl ethyl ketone 85dToluene 85-Cyclohexanone 301i! When thermal transfer was carried out in the same manner as in Example 1, an image recording with high transfer density was obtained.
実施例4
(熱転写受像材料(4)の作製)
下記(A)の組成のゼラチン水溶液中に(B)の組成の
色素受容性ポリマーの有機溶剤溶液をホモジナイザーで
乳化分散し色素受容性物質のゼラチン分散液を調製した
。Example 4 (Preparation of thermal transfer image-receiving material (4)) An organic solvent solution of a dye-receiving polymer having the composition of (B) was emulsified and dispersed in an aqueous gelatin solution of the following composition (A) using a homogenizer to obtain gelatin as a dye-receiving material. A dispersion was prepared.
(A)ゼラチン水溶液
ゼラチン 2.3gドデシルベ
ンゼンスルホン酸 20mナトリウム(5%水溶
液)
水
(B)色素受容性ポリマー溶液
ポリエステル樹脂
(東洋紡製:バイロン300)
カルボキシ変性シリコーンオイル
(信越シリコーン製: X−22
−3710)
メチルエチルケトン
0m1
7、0g
0゜ 7g
0d
トルエン 10dトリフエニ
ルフオスフエー) 1.5gこのようにして調製
した分散物のフッ素系界面活性材(a ) CzPq
SOJCIhCOOKの0.5gを水(CsPt)
/メタノール(1: 1)の混合溶媒10dに溶解した
溶液を添加し、受容層用塗布組成物とした。(A) Gelatin aqueous solution Gelatin 2.3g Dodecylbenzenesulfonic acid 20m Sodium (5% aqueous solution) Water (B) Dye-receptive polymer solution Polyester resin (Toyobo: Vylon 300) Carboxy-modified silicone oil (Shin-Etsu Silicone: X-22 -3710) Methyl ethyl ketone 0ml 7.0g 0゜ 7g 0d Toluene 10dTriphenyl phosphate) 1.5g Fluorine surfactant of the dispersion thus prepared (a) CzPq
A solution of 0.5 g of SOJCIhCOOK dissolved in 10 d of a mixed solvent of water (CsPt)/methanol (1:1) was added to prepare a coating composition for a receptor layer.
この塗布組成物を、表面にコロナ放電した厚み150p
mの合成紙(玉子油化製: YLJPO−3GG−15
0)上にワイヤーバーコーティング法によりウェット膜
厚75μmとなるように塗布し乾燥した。This coating composition was corona discharged onto the surface to a thickness of 150p.
m synthetic paper (manufactured by Tamago Yuka: YLJPO-3GG-15
0) by a wire bar coating method to a wet film thickness of 75 μm and dried.
得られた受像材料を用い実施例1及び2に記載の本発明
の色素供与材料を用い熱転写を行なったところ、高濃度
の記録が得られた。When thermal transfer was performed using the obtained image-receiving material and the dye-providing material of the present invention described in Examples 1 and 2, high-density recording was obtained.
Claims (1)
と該色素に対して30〜100重量%の量のバインダー
を含有する色素供与層を有してなる熱転写色素供与材料
。1. A thermal transfer dye-providing material comprising, on a support, a dye-donating layer containing at least a substantially amorphous heat-transferable dye and a binder in an amount of 30 to 100% by weight relative to the dye.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1264777A JPH03126589A (en) | 1989-10-11 | 1989-10-11 | Thermal transfer dye donating material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1264777A JPH03126589A (en) | 1989-10-11 | 1989-10-11 | Thermal transfer dye donating material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03126589A true JPH03126589A (en) | 1991-05-29 |
Family
ID=17408047
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1264777A Pending JPH03126589A (en) | 1989-10-11 | 1989-10-11 | Thermal transfer dye donating material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03126589A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001056805A1 (en) * | 2000-02-01 | 2001-08-09 | Polaroid Corporation | Thermal transfer recording system having an amorphous dye phase |
EP1493593A1 (en) * | 2000-02-01 | 2005-01-05 | Polaroid Corporation | Thermal transfer recording system having an amorphous dye phase |
US8833663B2 (en) | 2002-04-09 | 2014-09-16 | L-1 Secure Credentialing, Inc. | Image processing techniques for printing identification cards and documents |
-
1989
- 1989-10-11 JP JP1264777A patent/JPH03126589A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001056805A1 (en) * | 2000-02-01 | 2001-08-09 | Polaroid Corporation | Thermal transfer recording system having an amorphous dye phase |
US6537410B2 (en) | 2000-02-01 | 2003-03-25 | Polaroid Corporation | Thermal transfer recording system |
EP1493593A1 (en) * | 2000-02-01 | 2005-01-05 | Polaroid Corporation | Thermal transfer recording system having an amorphous dye phase |
JP2006001281A (en) * | 2000-02-01 | 2006-01-05 | Polaroid Corp | Thermal transfer recording system having amorphous dye phase |
US8833663B2 (en) | 2002-04-09 | 2014-09-16 | L-1 Secure Credentialing, Inc. | Image processing techniques for printing identification cards and documents |
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JPH03112685A (en) | Thermal transfer dyestuff-giving material | |
JPH02258389A (en) | Thermal transfer image receiving material | |
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JPH05294080A (en) | Thermal transfer image receiving material | |
JPH02276682A (en) | Thermal transfer image-receiving material | |
JPH0761147A (en) | Thermal transfer recording material | |
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JPH0371891A (en) | Thermal transfer image receiving material |