JPS62278089A - Electothermal transfer recording medium - Google Patents
Electothermal transfer recording mediumInfo
- Publication number
- JPS62278089A JPS62278089A JP61120971A JP12097186A JPS62278089A JP S62278089 A JPS62278089 A JP S62278089A JP 61120971 A JP61120971 A JP 61120971A JP 12097186 A JP12097186 A JP 12097186A JP S62278089 A JPS62278089 A JP S62278089A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- layer
- resin
- ink
- 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
- 229920005989 resin Polymers 0.000 claims abstract description 33
- 239000011347 resin Substances 0.000 claims abstract description 33
- 239000003086 colorant Substances 0.000 claims abstract description 15
- 239000000126 substance Substances 0.000 claims abstract description 14
- 239000007787 solid Substances 0.000 claims abstract description 5
- 238000002844 melting Methods 0.000 claims description 17
- 229920001577 copolymer Polymers 0.000 abstract description 4
- 239000012461 cellulose resin Substances 0.000 abstract description 3
- 229920005992 thermoplastic resin Polymers 0.000 abstract description 3
- 150000001336 alkenes Chemical class 0.000 abstract description 2
- 239000000470 constituent Substances 0.000 abstract 1
- 238000010276 construction Methods 0.000 abstract 1
- 229920001519 homopolymer Polymers 0.000 abstract 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 73
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 239000000049 pigment Substances 0.000 description 24
- 239000003921 oil Substances 0.000 description 22
- 235000019198 oils Nutrition 0.000 description 22
- 239000012943 hotmelt Substances 0.000 description 21
- 230000000052 comparative effect Effects 0.000 description 20
- 238000000034 method Methods 0.000 description 20
- 239000000203 mixture Substances 0.000 description 20
- 239000004166 Lanolin Substances 0.000 description 12
- 235000019388 lanolin Nutrition 0.000 description 12
- 229940039717 lanolin Drugs 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
- 239000006229 carbon black Substances 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 239000000975 dye Substances 0.000 description 9
- 239000001993 wax Substances 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- -1 polyethylene Polymers 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000000123 paper Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229940057995 liquid paraffin Drugs 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 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 3
- 229920006267 polyester film Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000000980 acid dye Substances 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000004760 aramid Substances 0.000 description 2
- 229920003235 aromatic polyamide Polymers 0.000 description 2
- 239000000981 basic dye Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000000982 direct dye Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000001454 recorded image Methods 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000000988 sulfur dye Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 239000011135 tin Substances 0.000 description 2
- 239000000984 vat dye Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- IJAAWBHHXIWAHM-PHEQNACWSA-N 1,4-bis[(e)-2-phenylethenyl]benzene Chemical compound C=1C=CC=CC=1/C=C/C(C=C1)=CC=C1\C=C\C1=CC=CC=C1 IJAAWBHHXIWAHM-PHEQNACWSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- WCOXQTXVACYMLM-UHFFFAOYSA-N 2,3-bis(12-hydroxyoctadecanoyloxy)propyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC(O)CCCCCC)COC(=O)CCCCCCCCCCC(O)CCCCCC WCOXQTXVACYMLM-UHFFFAOYSA-N 0.000 description 1
- GNCOVOVCHIHPHP-UHFFFAOYSA-N 2-[[4-[4-[(1-anilino-1,3-dioxobutan-2-yl)diazenyl]-3-chlorophenyl]-2-chlorophenyl]diazenyl]-3-oxo-n-phenylbutanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC(C(=C1)Cl)=CC=C1C(C=C1Cl)=CC=C1N=NC(C(C)=O)C(=O)NC1=CC=CC=C1 GNCOVOVCHIHPHP-UHFFFAOYSA-N 0.000 description 1
- LHYQAEFVHIZFLR-UHFFFAOYSA-L 4-(4-diazonio-3-methoxyphenyl)-2-methoxybenzenediazonium;dichloride Chemical compound [Cl-].[Cl-].C1=C([N+]#N)C(OC)=CC(C=2C=C(OC)C([N+]#N)=CC=2)=C1 LHYQAEFVHIZFLR-UHFFFAOYSA-L 0.000 description 1
- CQPBLBQMIFRGLU-UHFFFAOYSA-N 4-(6-azabicyclo[3.1.1]hepta-1(7),2,4-triene-6-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1C2=CC=CC1=C2 CQPBLBQMIFRGLU-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- ATJXMQHAMYVHRX-CPCISQLKSA-N Ellagic acid Natural products OC1=C(O)[C@H]2OC(=O)c3cc(O)c(O)c4OC(=O)C(=C1)[C@H]2c34 ATJXMQHAMYVHRX-CPCISQLKSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241000219745 Lupinus Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- GOWVWFPZYWGIPA-UHFFFAOYSA-N N-(2-chlorophenyl)-4-[[7-[[3-[(2-chlorophenyl)carbamoyl]-2-hydroxynaphthalen-1-yl]diazenyl]-9-oxofluoren-2-yl]diazenyl]-3-hydroxynaphthalene-2-carboxamide Chemical compound Oc1c(cc2ccccc2c1N=Nc1ccc2-c3ccc(cc3C(=O)c2c1)N=Nc1c(O)c(cc2ccccc12)C(=O)Nc1ccccc1Cl)C(=O)Nc1ccccc1Cl GOWVWFPZYWGIPA-UHFFFAOYSA-N 0.000 description 1
- LMULDSDQRQVZMW-UHFFFAOYSA-N N-(5-chloro-2,4-dimethoxyphenyl)-4-[[5-(diethylsulfamoyl)-2-methoxyphenyl]diazenyl]-3-hydroxynaphthalene-2-carboxamide Chemical compound CCN(CC)S(=O)(=O)C1=CC=C(OC)C(N=NC=2C3=CC=CC=C3C=C(C=2O)C(=O)NC=2C(=CC(OC)=C(Cl)C=2)OC)=C1 LMULDSDQRQVZMW-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- WLDHEUZGFKACJH-UHFFFAOYSA-K amaranth Chemical compound [Na+].[Na+].[Na+].C12=CC=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(O)=C1N=NC1=CC=C(S([O-])(=O)=O)C2=CC=CC=C12 WLDHEUZGFKACJH-UHFFFAOYSA-K 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- JPIYZTWMUGTEHX-UHFFFAOYSA-N auramine O free base Chemical compound C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1 JPIYZTWMUGTEHX-UHFFFAOYSA-N 0.000 description 1
- QFFVPLLCYGOFPU-UHFFFAOYSA-N barium chromate Chemical compound [Ba+2].[O-][Cr]([O-])(=O)=O QFFVPLLCYGOFPU-UHFFFAOYSA-N 0.000 description 1
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- HBHZKFOUIUMKHV-UHFFFAOYSA-N chembl1982121 Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O HBHZKFOUIUMKHV-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000003273 ketjen black Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- RVWOWEQKPMPWMQ-UHFFFAOYSA-N methyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OC RVWOWEQKPMPWMQ-UHFFFAOYSA-N 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000983 mordant dye Substances 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000011088 parchment paper Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229940043267 rhodamine b Drugs 0.000 description 1
- OARRHUQTFTUEOS-UHFFFAOYSA-N safranin Chemical compound [Cl-].C=12C=C(N)C(C)=CC2=NC2=CC(C)=C(N)C=C2[N+]=1C1=CC=CC=C1 OARRHUQTFTUEOS-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- ZHFPEICFUVWJIS-UHFFFAOYSA-M sodium 2-hydroxy-5-[(3-nitrophenyl)diazenyl]benzoate Chemical compound [Na+].Oc1ccc(cc1C([O-])=O)N=Nc1cccc(c1)[N+]([O-])=O ZHFPEICFUVWJIS-UHFFFAOYSA-M 0.000 description 1
- AXMCIYLNKNGNOT-UHFFFAOYSA-M sodium;3-[[4-[(4-dimethylazaniumylidenecyclohexa-2,5-dien-1-ylidene)-[4-[ethyl-[(3-sulfonatophenyl)methyl]amino]phenyl]methyl]-n-ethylanilino]methyl]benzenesulfonate Chemical compound [Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](C)C)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 AXMCIYLNKNGNOT-UHFFFAOYSA-M 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 235000012756 tartrazine Nutrition 0.000 description 1
- UJMBCXLDXJUMFB-GLCFPVLVSA-K tartrazine Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-GLCFPVLVSA-K 0.000 description 1
- 239000004149 tartrazine Substances 0.000 description 1
- 229960000943 tartrazine Drugs 0.000 description 1
- OLSOUGWNONTDCK-UHFFFAOYSA-J tetrasodium 5-amino-3-[[4-[4-[(8-amino-1-hydroxy-3,6-disulfonatonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-4-hydroxynaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(N=NC3=CC=C(C=C3OC)C=3C=C(C(=CC=3)N=NC=3C(=CC4=CC(=CC(N)=C4C=3O)S([O-])(=O)=O)S([O-])(=O)=O)OC)=C(O)C2=C1N OLSOUGWNONTDCK-UHFFFAOYSA-J 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- LLWJPGAKXJBKKA-UHFFFAOYSA-N victoria blue B Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC(=CC=1)N(C)C)=C(C=C1)C2=CC=CC=C2C1=[NH+]C1=CC=CC=C1 LLWJPGAKXJBKKA-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- 229940012185 zinc palmitate Drugs 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
- GJAPSKMAVXDBIU-UHFFFAOYSA-L zinc;hexadecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O GJAPSKMAVXDBIU-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/3825—Electric current carrying heat transfer sheets
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Impression-Transfer Materials And Handling Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【発明の詳細な説明】
3、発明の詳細な説明
し技術分野]
本発明は、通電により発生する熱によって記録画像を転
写する通電感熱転写記録媒体に関する。Detailed Description of the Invention 3. Detailed Description of the Invention and Technical Field] The present invention relates to an electrically conductive thermal transfer recording medium that transfers a recorded image using heat generated by electrical conduction.
[従来技術]
近年、熱転写記録はノンインパクトで無騒音、メンテナ
ンスフリー、低コスト、小型軽量化可能、カラー化可能
等の特徴を有するために、ファクシミリ、コンピュータ
一端末、レコーダー等の多くの分野で注目されてきた。[Prior art] In recent years, thermal transfer recording has been used in many fields such as facsimiles, computer terminals, recorders, etc. because it has the characteristics of being non-impact, noiseless, maintenance-free, low cost, small and lightweight, and can be colored. It has been attracting attention.
その内でも、特に通電ヘッドにより通電熱転写する方法
は、中間階調を有するフルカラー記録に適しており、将
来の有力なハードコピーとして最も注目されている方式
である。そして、例えば「日経エレクトロニクス」64
〜68頁、6月25日号、1979年に紹介された方式
および特開昭60−78785号公報に記載された方式
等が知られているが、得られる画像の階調性に関しては
、濃度階調法をもつ昇華型熱転写記録方式と比較すると
未だ満足するには至っていない。Among these methods, the method of thermal transfer using a current-carrying head is particularly suitable for full-color recording with intermediate gradation, and is the method that is attracting the most attention as a promising future hard copy method. For example, "Nikkei Electronics" 64
- Page 68, June 25 issue, the method introduced in 1979 and the method described in Japanese Patent Application Laid-Open No. 60-78785 are known, but regarding the gradation of the obtained image, the density Compared to the sublimation thermal transfer recording method which uses a gradation method, it is still not satisfactory.
[目 的]
本発明は、通電熱転写記録において、階調性の優れた記
録画像を得ることを目的とするものである。[Objective] The object of the present invention is to obtain a recorded image with excellent gradation in electrical thermal transfer recording.
[構 成]
本発明は、通電によりジュール熱を発生する支持体層お
よびインク層を有する記録媒体において、該インク層は
樹脂からなる微細多孔質組織中に常温では固体の熱溶融
性物質と着色剤とを主成分とする熱溶融インク成分を含
有した構造からなることを特徴とする通電感熱転写記録
媒体である。[Structure] The present invention provides a recording medium having a support layer and an ink layer that generate Joule heat when energized. This is an electrically conductive thermal transfer recording medium characterized by having a structure containing a heat-melting ink component whose main component is an agent.
この構成を図面に基づいて説明すると、第1図はその一
例で支持体1の一面に通電抵抗層2を、細面にインク層
3を設けたものである。このインク層3は樹脂からなる
微細多孔質組織4中に熱溶融インク成分5を含有したも
のである。This structure will be explained based on the drawings. FIG. 1 shows one example in which a current-carrying resistance layer 2 is provided on one surface of a support 1 and an ink layer 3 is provided on a narrow surface. This ink layer 3 contains a heat-melting ink component 5 in a microporous structure 4 made of resin.
第2図は他の例で1゛は中抵抗支持体でその一面に通電
抵抗層2およびインク層3を順次設けたものである。第
3図は中抵抗支持体1°の一面に通電層6を設け、他に
通電抵抗層2およびインク層3を順次設けたものである
。FIG. 2 shows another example in which 1' is a medium-resistance support, on one surface of which a current-carrying resistance layer 2 and an ink layer 3 are sequentially provided. In FIG. 3, a current-carrying layer 6 is provided on one surface of a medium resistance support 1°, and a current-carrying resistance layer 2 and an ink layer 3 are sequentially provided on the other side.
そして、かかる記録媒体を用いて画像記録をするには第
4図に示すように記録媒体と受容シート7とを重ね、記
録媒体の通電抵抗層2側に通電ヘッド8を抑圧接触させ
て通電し、通電抵抗層2を発熱させて昇温加熱し、支持
体1層を熱が伝達してインク層3が昇温し、インク成分
5が微細多孔質組織4の内部より溶融流動することによ
り、受容シート5側に熱転写記録されるものである。To record an image using such a recording medium, as shown in FIG. 4, the recording medium and the receiving sheet 7 are overlapped, and the current-carrying head 8 is pressed into contact with the current-carrying resistance layer 2 side of the recording medium to apply electricity. , the current-carrying resistance layer 2 is heated to generate heat, the heat is transmitted through the support layer 3, the temperature of the ink layer 3 is raised, and the ink component 5 melts and flows from inside the microporous structure 4. This is thermal transfer recording on the receiving sheet 5 side.
第4図は前記第1図に示したものを用い例で説明したも
のであるが、第2図の場合には通電が中抵抗支持体1°
を通じて行なわれ、又、第3図の場合には、通電が通電
層6および中抵抗支持体1°を通じて行なわれる。Fig. 4 is an example of what is shown in Fig. 1, but in the case of Fig. 2, the current is applied to the medium resistance support at 1°.
3, and in the case of FIG. 3 the current is passed through the current-carrying layer 6 and the medium resistance support 1°.
上記において、通電による熱エネルギーによって溶融し
、微細多孔質組織4からにじみ出るインク成分5の量は
、通電によって印加される熱エネルギー量によって変り
、この通電熱エネルギー量を制御することによって、転
写される着色剤の量を変化させることができ、階調を忠
実にかつ広く表わした画像で、かつきめの細かい鮮明な
画像を得ることができる。In the above, the amount of the ink component 5 that is melted by the thermal energy caused by energization and oozes out from the microporous structure 4 varies depending on the amount of thermal energy applied by energization, and by controlling the amount of energized thermal energy, the amount of ink component 5 that is transferred is transferred. The amount of colorant can be varied, and it is possible to obtain sharp, detailed images with faithful and wide gradations.
インク層における微細多孔質組織を形成する樹脂として
は、ポリ塩化ビニル、ポリ酢酸ビニル、塩ビー酢ビー共
重合体、セルロース系樹脂、ポリエステル系樹脂、ポリ
スチレン、フェノール樹脂、アルキッド樹脂、エポキシ
樹脂等が用いられる。ただし後述するオイルとの関係で
、多孔質を形成しやすいものは、塩ビー酢ビ共重合体、
酢酸セルロース、酪酸・酢酸セルロース、ニトロセルロ
ース等のセルロース系樹脂が好ましい。又、100℃以
上の耐熱性をもつものが良い。Examples of resins that form the microporous structure in the ink layer include polyvinyl chloride, polyvinyl acetate, vinyl chloride-vinyl acetate copolymer, cellulose resin, polyester resin, polystyrene, phenol resin, alkyd resin, and epoxy resin. used. However, due to the relationship with the oil described below, those that tend to form porosity are vinyl chloride vinyl acetate copolymer,
Cellulose resins such as cellulose acetate, cellulose butyrate/cellulose acetate, and nitrocellulose are preferred. Also, it is preferable to have heat resistance of 100°C or higher.
インク成分は常温で固体の熱溶融性物質と着色剤を主成
分とするが、熱溶融性物質としては、例えばカルナウバ
ワックス、パラフィンワックス、ザゾールワックス、マ
イクロクリスタリンワックス、カスターワックス、ラノ
リン等のワックス類、ステアリン酸、パルミチン酸、ラ
ウリン酸、ステアリン酸アルミニウム、ステアリン酸鉛
、ステアリン酸バリウム、ステアリン酸亜鉛、パルミチ
ン酸亜鉛、メチルヒドロキシステアレート、グリセロー
ルモノじドロキシステアレート等の高級脂肪酸あるいは
その金属塩、エステル等の誘導体;ポリエチレン、ポリ
プロピレン、ポリイソブチレン、ポリエチレンワックス
、酸化ポリエチレン、ポリ四フッ化エチレン、エチレン
−アクリル酸共重合体、エチレン−アクリル酸エチル共
重合体、■チレンー酢酸ビニル共重合体等のオレフィン
の単独または共重合体あるいはこれらの誘導体等からな
る熱可塑性樹脂などが用いられる。The ink components are mainly composed of heat-melting substances and colorants that are solid at room temperature. Examples of heat-melting substances include carnauba wax, paraffin wax, zazol wax, microcrystalline wax, castor wax, and lanolin. Higher fatty acids such as waxes, stearic acid, palmitic acid, lauric acid, aluminum stearate, lead stearate, barium stearate, zinc stearate, zinc palmitate, methyl hydroxystearate, glycerol monodiroxystearate, etc. Derivatives of metal salts, esters, etc.; polyethylene, polypropylene, polyisobutylene, polyethylene wax, polyethylene oxide, polytetrafluoroethylene, ethylene-acrylic acid copolymer, ethylene-ethyl acrylate copolymer, ethylene-vinyl acetate copolymer Thermoplastic resins made of single or copolymers of olefins, such as polymers, or derivatives thereof, are used.
以上の熱溶融性物質は単独でまたは二種以上混合して、
微細多孔質層を構成する樹脂100部に対して20〜2
DO部の割合で用いられる。The above heat-melting substances may be used alone or in combination of two or more,
20 to 2 parts per 100 parts of resin constituting the microporous layer
It is used in the proportion of DO part.
着色剤としては、昇華しない着色染料及び着色顔料が挙
げられるが、染料の方がより好ましい階調性ある画像が
1qられる。Examples of the coloring agent include colored dyes and colored pigments that do not sublimate, but dyes are more preferable for images with gradation.
このような着色染料として、下記の直接染料、酸性染料
、塩基性染料、tJX染染料、硫化染料、建染染料、ア
ゾイック染料、油性染料等がある。Examples of such coloring dyes include the following direct dyes, acid dyes, basic dyes, tJX dyes, sulfur dyes, vat dyes, azoic dyes, and oil dyes.
1)直接染料;ダイレクトスカイブルー、ダイレクトブ
ラックW等。1) Direct dyes; Direct Sky Blue, Direct Black W, etc.
2)酸性染料:タートラジン、アシッドバイオレッド6
B、アシドフ7ストレツS 3G等。2) Acid dye: Tartrazine, Acid Violet 6
B, Ashidov 7 Strets S 3G, etc.
3)塩基性染料:サフラニン、オーラミン、クリスタル
バイオレット、メチレンブルー、ロ−ダミンB、ビクト
リアブルーB等。3) Basic dyes: safranin, auramine, crystal violet, methylene blue, rhodamine B, Victoria blue B, etc.
4)媒染染料:サンクロミンファーストブルーMB、エ
リオフロムアズロールB1アリザリンイエローB等。4) Mordant dyes: Sunchromin Fast Blue MB, Elio from Azurol B1 Alizarin Yellow B, etc.
5)硫化染料:サルファブリリアントグリーン4G等。5) Sulfur dye: Sulfur Brilliant Green 4G, etc.
6)建染染料:インダンスレンブル−等。6) Vat dyes: indanthremble, etc.
7)アゾイック染料:ナフトールAs等。7) Azoic dyes: naphthol As, etc.
8)油性染料:ニグロシン、スピリットブラックEB、
バリファストオレンジ3206、オイルブラック215
、バターイエロー、スーダンブルー■、オイルレッド8
10−ダミンB等。8) Oil dye: Nigrosine, Spirit Black EB,
Varifast Orange 3206, Oil Black 215
, Butter Yellow, Sudan Blue ■, Oil Red 8
10-Damin B et al.
これらの染料は好ましくは溶解状態であるのがよい。These dyes are preferably in a dissolved state.
着色顔料としては、着色微粒子顔料、モノアゾ顔料等が
挙げられる。着色微粒子顔料としては下記のものが例示
できる。いずれもヘキスF製のもので、かっこ内はカラ
ーインデックスNo、を示す。Examples of colored pigments include colored fine particle pigments and monoazo pigments. Examples of colored fine particle pigments include the following. All of them are made by Hex F, and the color index numbers are shown in parentheses.
パーマネント イエローGG、2(ピグメントイエロー
17)、パーマネント イエローDHGトランス02
(ピグメント イエロー12)、ノボパーム イエロー
HRO3(ピグメント イエロー83) 、ハンザ ブ
リリアント イエロー5GXO2(ピグメント イエロ
ー74)、パーマネント オレンジRLOI(ピグメン
ト オレンジ34)、ノボパーム レッド1−IFG(
ピグメント オレンジ38)、ノボパーム レッドHF
T(ピグメント レッド175) 、パーマネント レ
ークレッドLCLLO2(ピグメント レッド53:1
)、ノボパーム レッドHF4B(ピグメントレッド1
87) 、パーマネント カルミンFB[302(ピグ
メント レッド14B) 、パーマネント ルピンL6
B(ピグメント レッド57 : 1)、ホスタパーム
ピンクEトランス(ピグメントレッド122) 、レ
フレックス ブルーR50(ピグメント ブルー61)
又、モノアゾ顔料としては、下記の構造式で表わされる
化合物である。Permanent Yellow GG, 2 (Pigment Yellow 17), Permanent Yellow DHG Transformer 02
(Pigment Yellow 12), Novopalm Yellow HRO3 (Pigment Yellow 83), Hansa Brilliant Yellow 5GXO2 (Pigment Yellow 74), Permanent Orange RLOI (Pigment Orange 34), Novopalm Red 1-IFG (
Pigment Orange 38), Novopalm Red HF
T (Pigment Red 175), Permanent Lake Red LCLLO2 (Pigment Red 53:1)
), Novopalm Red HF4B (Pigment Red 1
87), Permanent Carmine FB [302 (Pigment Red 14B), Permanent Lupine L6
B (Pigment Red 57: 1), Hostapalm Pink E Trans (Pigment Red 122), Reflex Blue R50 (Pigment Blue 61) In addition, monoazo pigments include compounds represented by the following structural formula.
X−N=N−Y ただし、 Xニジアゾニウム塩残基 Y:カップラー残基 特に商品名で具体的に例示すると、下記のものがある。X-N=N-Y however, X didiazonium salt residue Y: coupler residue Particularly specific examples of product names include the following.
(1) 5ico Fast Yellow D 13
55 (BAS F製)(2) 5ico Fast
Yellow D 1250 (BAS F製)(3)
Lake Red LC(Hoechst製)構造式
は
(4) Lake Red C405(大日精化製〉(
5) Fast Red 1547 (大日精化製)
上記したような構造を有するインク層の製造法は特に限
定されるものではないが、一般には次のような方法が取
られる。すなわち、熱溶融性物質及び着色剤と、樹脂の
多孔質を形成する役目をするオイルとを、適当な有機溶
剤と共に、アトライター及びボールミル等のような分散
装置を用いて混合、分散させインク分散液(溶液でもよ
い)を得る。別途、有機溶剤に溶解させた樹脂の溶液を
得、これを前記インク分散液とともに混合し、ボールミ
ル等の混和器で均一に分散する。次いで得られた分散液
を支持体上に塗布し、乾燥することにより前記のような
微細構造の熱溶融インク層が得られる。分散液中には、
前記した熱溶融性物質、着色剤とオイルの分散をよくす
るため(湿潤剤、分散剤等を加えてもよい。また必要に
応じて、この種の樹脂塗料に通常使用される充填剤を加
えることもできる。(1) 5ico Fast Yellow D 13
55 (made by BASF) (2) 5ico Fast
Yellow D 1250 (made by BASF F) (3)
The structural formula of Lake Red LC (manufactured by Hoechst) is (4) Lake Red C405 (manufactured by Dainichiseika) (
5) Fast Red 1547 (manufactured by Dainichiseika)
Although the method for producing the ink layer having the above-described structure is not particularly limited, the following method is generally used. That is, the ink is dispersed by mixing and dispersing a heat-fusible substance, a coloring agent, and an oil that serves to form the porosity of the resin together with an appropriate organic solvent using a dispersion device such as an attritor or a ball mill. Obtain a liquid (or a solution). Separately, a solution of the resin dissolved in an organic solvent is obtained, mixed with the ink dispersion, and uniformly dispersed using a mixer such as a ball mill. Next, the resulting dispersion is applied onto a support and dried to obtain a hot-melt ink layer having the above-mentioned fine structure. In the dispersion,
In order to improve the dispersion of the above-mentioned heat-melting substances, colorants and oils (wetting agents, dispersants, etc. may be added), if necessary, fillers commonly used in this type of resin paint may be added. You can also do that.
また別法として、多孔質組織を形成する樹脂とは非相溶
性であり該樹脂を溶解しない溶媒に可溶性であり物質を
樹脂とともに混練し、支持体上に塗布して樹脂層を形成
したのち該物質を前記のような溶媒で溶解して多孔質樹
脂組織を形成し、更にその多孔質組織中に熱溶融インク
成分を充填する方法によっても上記したような構造を有
する熱溶融インク層が得られる。Alternatively, a substance that is incompatible with the resin that forms the porous structure and is soluble in a solvent that does not dissolve the resin is kneaded with the resin and coated on a support to form a resin layer. A hot-melt ink layer having the above-described structure can also be obtained by dissolving a substance in the above-mentioned solvent to form a porous resin structure, and then filling the porous structure with hot-melt ink components. .
この厚さとしては1〜30μ、好ましくは2〜20μが
挙げられる。This thickness may be 1 to 30 microns, preferably 2 to 20 microns.
オイルとしては、上記したような熱可塑性樹脂と非相溶
性であり、非揮発性のものであれば、液体、半固体のい
ずれも用いられる。液体オイルとしては、たとえば綿実
油、菜種油、鯨油等の動植物油;あるいはモーターオイ
ル、スピンドル油、ダイナモ油等の鉱油が、また半固体
オイルとしては、たとえばラノリン、ラノリン誘導体、
ワセリン、ラード等が用いられる。As the oil, any liquid or semi-solid oil can be used as long as it is incompatible with the above-mentioned thermoplastic resin and is non-volatile. Liquid oils include, for example, animal and vegetable oils such as cottonseed oil, rapeseed oil, and whale oil; mineral oils such as motor oil, spindle oil, and dynamo oil; and semisolid oils include, for example, lanolin, lanolin derivatives,
Vaseline, lard, etc. are used.
このオイルに関しては好ましくはラノリン誘導体オイル
であり、さらに好ましくはラノリン脂肪酸又はラノリン
脂肪酸エステルのオイルであり、市販されているものの
具体例としては、ネオコート0ES−181,0ES1
83 、LFC−50M、 LS−3102MB (以
上吉川製油)などが挙げられる。This oil is preferably a lanolin derivative oil, more preferably an oil of lanolin fatty acid or lanolin fatty acid ester, and specific examples of commercially available oils include Neocoat 0ES-181 and 0ES1.
83, LFC-50M, and LS-3102MB (all manufactured by Yoshikawa Oil Co., Ltd.).
11一
本発明に用いる支持体としては、従来より公知のフィル
ムや紙をそのまま使用することができ、例えばポリエス
テル、ポリカーボネート、トリアセチルセルロース、ナ
イロン、ポリイミド、芳香族ポリアミド等の比較的耐熱
性の良いプラスチックのフィルム、セロハンあるいは硫
酸紙などが好適に使用できる。支持体の厚さは熱転写に
際しての通電によるジュール熱の伝導効率を考慮すると
、2〜15ミクロン程度であることが望ましい。11. As the support used in the present invention, conventionally known films and papers can be used as they are, for example, materials with relatively good heat resistance such as polyester, polycarbonate, triacetylcellulose, nylon, polyimide, aromatic polyamide, etc. Plastic film, cellophane, parchment paper, etc. can be suitably used. The thickness of the support is desirably about 2 to 15 microns in consideration of the conduction efficiency of Joule heat due to energization during thermal transfer.
又、前記第2図における中抵抗支持体としては上記比較
的耐熱性の良い樹脂をバインダーとして、主として導電
剤であるカーボンブラックを主成分として含有したシー
ト状物が使用される。ここでバインダー樹脂とカーボン
ブラックとの割合は重量比で前者が70〜97%、後者
が3〜30%が適当である。中抵抗の値としては体積固
有抵抗103〜108Ω−cm、表面抵抗108〜10
12Ω/口が望まれる。Further, as the medium resistance support in FIG. 2, a sheet-like material containing the above-mentioned relatively heat-resistant resin as a binder and carbon black as a main component, which is a conductive agent, is used. Here, the proportion of the binder resin and carbon black is suitably 70 to 97% by weight for the former and 3 to 30% for the latter. Medium resistance values are volume resistivity 103~108 Ω-cm, surface resistance 108~10
12 Ω/mouth is desired.
通電抵抗層は通電により発熱する機能をもだせる層で、
その抵抗値は、絶縁体と良導体の中間の抵抗値を有する
必要があり、抵抗値は、通電電力量、記録シートの熱伝
導率、インク層の融解エネルギー等のバランスで設定さ
れる。通電抵抗層を発熱させるために、従来から、アル
ミニウム、銅、鉄、錫、亜鉛、ニッケル、モリブデン、
銀等の金属粉を樹脂バインダー中に分散させて抵抗層を
形成する方法(特開昭56−86790〜特開昭56−
86793)、沃化鋼を樹脂バインダー中に分散させる
方法(特開昭5l−106445)、酸化亜鉛、二酸化
チタンを樹脂バインダー中に分散させる方法(特開昭5
3−74047)、導電性ポリマーを支持体層に塗布す
る方法(特開昭5l−106445) 、グラファイト
、アセチレンブラックを樹脂バインダーに分散する方法
(特公昭56−27382)、低抵抗化カーボンブラッ
ク(特開昭60−71293)ざらにアルミニウム、銅
、鉄、亜鉛、錫、ニッケル、モリブデン、銀等の金属を
蒸着またはスパッタリングして、支持体層に塗布する方
法等が提案されており、いずれの方法でも構わないが、
通電抵抗層はその抵抗値を小ざくすればするほど、通電
ヘッドの印加電圧を小さくでき、従って電源とヘッドの
駆動系は容量を小さくでき、信頼性が増し安価にできる
。The current-carrying resistance layer is a layer that can generate heat when energized.
The resistance value must be between that of an insulator and a good conductor, and the resistance value is set based on the balance of the amount of electric power applied, the thermal conductivity of the recording sheet, the melting energy of the ink layer, etc. Conventionally, aluminum, copper, iron, tin, zinc, nickel, molybdenum,
A method of forming a resistance layer by dispersing metal powder such as silver in a resin binder (JP-A-56-86790 - JP-A-56-
86793), a method of dispersing iodized steel in a resin binder (Japanese Patent Application Laid-Open No. 51-106445), a method of dispersing zinc oxide and titanium dioxide in a resin binder (Japanese Patent Application Laid-Open No. 51-1993)
3-74047), a method of applying a conductive polymer to a support layer (JP-A-51-106445), a method of dispersing graphite and acetylene black in a resin binder (JP-B No. 56-27382), low-resistance carbon black (JP-A-56-27382), JP-A-60-71293) A method has been proposed in which metals such as aluminum, copper, iron, zinc, tin, nickel, molybdenum, and silver are coated on the support layer by vapor deposition or sputtering. Any method is fine, but
The smaller the resistance value of the current-carrying resistance layer is, the smaller the voltage applied to the current-carrying head can be.Therefore, the capacity of the power supply and head drive system can be reduced, making it more reliable and less expensive.
従って表面抵抗値は106Ω/ロ以下が好ましく、ざら
には5X105Ω/口以下にすることが望まれる。Therefore, the surface resistance value is preferably 10 6 Ω/lower or less, and more preferably 5×10 5 Ω/lower.
第3図における通電層、中抵抗支持体、導電層は、それ
ぞれ銅等の金属粉または導電性の異なるカーボン等の種
類又はその量の大小によつ上記層には比較的耐熱性の良
いポリエステル、ポリカーボネート、トリアセチルセル
ロース、ナイロン、ポリイミド、芳香族ポリアミド等の
樹脂が用いられる。The current-carrying layer, medium-resistance support, and conductive layer in FIG. , polycarbonate, triacetylcellulose, nylon, polyimide, aromatic polyamide, and other resins are used.
また本発明で得られる階調性をさらに向上させるために
、後記する階調制御剤を加えることも可能である。Further, in order to further improve the gradation obtained by the present invention, it is also possible to add a gradation control agent to be described later.
その他前記多孔質樹脂組織をより強く保持するために、
あらかじめ支持体上に中間接着層を設けておくことも可
能である。In order to maintain the porous resin structure more strongly,
It is also possible to provide an intermediate adhesive layer on the support in advance.
中間接着層としては、いわゆるプラスデック樹脂および
プラスチック樹脂に充填剤を添加したものが挙げられる
。Examples of the intermediate adhesive layer include so-called Plusdec resins and plastic resins with fillers added thereto.
受容シートは、基本的には普通紙、合成紙でよいが、必
要とあれば、上記樹脂またはTiO2、シリカ、ZnO
等の充填剤を含有したものを普通紙上に塗布して、着色
剤の転移が容易になるように工夫することも可能である
。The receiving sheet may basically be plain paper or synthetic paper, but if necessary, it may be made of the above resins, TiO2, silica, ZnO.
It is also possible to apply a filler containing fillers such as the like on plain paper to facilitate the transfer of the colorant.
前述の階調制御剤は、熱溶融インクの主成分となるオイ
ル、ワックス等の低融点物質よりも樹脂との濡れ、相溶
性が良く、スポンジ樹脂構進中に堅固に保持され、その
存在によって多孔質組織の孔径をより小さくするように
微妙にコントロールするものである。従ってそれ自身、
熱エネルギーを印加しても転出されず、多孔質組織中に
保持され、周辺に存在する着色剤、インクの転移する量
をコントロールするという良好なる階調制御剤の働きを
するものと考えられる。The aforementioned gradation control agent has better wettability and compatibility with the resin than low-melting substances such as oil and wax, which are the main components of hot-melt ink, and is firmly held in the sponge resin structure. This is to delicately control the pore size of the porous structure to make it smaller. Therefore itself,
It is thought that it is not transferred out even when thermal energy is applied, is retained in the porous structure, and functions as a good gradation control agent by controlling the amount of colorant and ink existing in the surrounding area that transfers.
かかる階調制御剤としては、以下の物が具体例として示
される。Specific examples of such gradation control agents include the following.
針状結晶顔料:
無機質、有機質のもの何れも使用可能であり、それらの
具体例を示すと、黄土(オーカー)、黄鉛01ツタ日シ
アニンブルー、リソールレッド、ボンマルトーンライト
、白土、針状酸化亜鉛、2.7−ビス[2−ヒドロキシ
−3−(2−クロルフェニルカルバモイル)ナフタレン
−1−イルアゾ]−9−フルオレノン、4“、4°′−
ビス[ヒドロキシ−3−(2,4−ジメチルフェニル)
カルバモイルナフタレン−1−イルアゾ)1.4−ジス
チリルベンゼン等が挙げられるが、結晶が針状で、それ
らが転写層中で網状構造に配列するような物質であれば
どれでも使用できる。Acicular crystal pigments: Both inorganic and organic substances can be used, and specific examples include ocher, yellow lead 01 ivy sun cyanine blue, lithore red, Bonmartone light, white clay, and needle crystal pigments. Zinc oxide, 2,7-bis[2-hydroxy-3-(2-chlorophenylcarbamoyl)naphthalen-1-ylazo]-9-fluorenone, 4", 4°'-
Bis[hydroxy-3-(2,4-dimethylphenyl)
Examples include carbamoylnaphthalen-1-ylazo)1,4-distyrylbenzene, but any material can be used as long as the crystals are acicular and the crystals are arranged in a network structure in the transfer layer.
アゾ系顔料:
例えば下記の如き化学構造式を有するものを用いること
ができる。Azo pigment: For example, one having the following chemical structural formula can be used.
X−+N=N−Y)n 式中、Xニジアゾニウム塩残基 Y二カップラー残基 n:1.2、又は3 代表例としては、以下の如きものが挙げられる。X-+N=N-Y)n In the formula, X didiazonium salt residue Y dicoupler residue n: 1.2 or 3 Representative examples include the following.
ト(昌
しn3
し1
一 24−
フタロシアニン系顔料:
メタルフリーフタロシアニン及びその誘導体、メタルフ
タロシアニン及びその誘導体が使用可能であり、これら
の具体例としては以下のものが例示される。24- Phthalocyanine pigment: Metal-free phthalocyanine and its derivatives, metal phthalocyanine and its derivatives can be used, and specific examples thereof include the following.
上記階調制御剤の添加量は着色剤1重量部に対して0.
5〜10重量部、好ましくは1〜5重量部である。The amount of the gradation control agent added is 0.000% per 1 part by weight of the colorant.
The amount is 5 to 10 parts by weight, preferably 1 to 5 parts by weight.
次に実施例並びに比較例によって本発明を説明する、部
、%はいずれも重量基準である。Next, the present invention will be explained with reference to Examples and Comparative Examples. All parts and percentages are based on weight.
実施例1
下記組成よりなる通電抵抗層形成液を、ボールミルで約
24時量子分混合し、ワイヤーバーを用いて厚さ6μm
のポリエステルフィルムの表面に塗布し、乾燥温度10
0℃で1分間乾燥して厚さ4μmの通電抵抗層を形成し
た。Example 1 A current-carrying resistance layer forming liquid having the following composition was mixed for about 24 hours using a ball mill, and then formed to a thickness of 6 μm using a wire bar.
Coated on the surface of a polyester film and dried at a temperature of 10
It was dried at 0° C. for 1 minute to form a current carrying resistance layer with a thickness of 4 μm.
カーボンブラック:
(コロンビアカーボン製Pr1ntex 90) 30
部塩ビー酢ビ共重合体 80部M E K
200部トルエン
200部次いで下記組成の熱溶
融インキ成分をメチルエチルケトン175部とトルエン
250部の混合液とともにボールミルで約24時間時間
分散させる。Carbon black: (Columbia Carbon Pr1ntex 90) 30
80 parts salt vinyl vinyl acetate copolymer M E K
200 parts toluene
Next, 200 parts of the hot melt ink component having the composition shown below is dispersed in a ball mill for about 24 hours with a mixed solution of 175 parts of methyl ethyl ketone and 250 parts of toluene.
ラノリン脂肪酸オイル
(OES−183、吉川製油製)30部カルナウバワッ
クス(トルエン20%混合液)30部
パラフィンワックス(トルエン20%混合液)30部
着色剤(BASF製、Neozapon Blue 8
07)30部
分散剤 1部流動パラフィ
ン 10部次いで20%の塩ビー酢ビ
共重合体樹脂溶液(樹脂10部、トルエン20部、メチ
ルエチルケトン20部)450部を上記インキ分散液に
加え、約1時間ボールミルによって分散し、感熱転写組
成物の塗剤を作成した。Lanolin fatty acid oil (OES-183, manufactured by Yoshikawa Oil Co., Ltd.) 30 parts Carnauba wax (20% toluene mixture) 30 parts Paraffin wax (20% toluene mixture) 30 parts Colorant (manufactured by BASF, Neozapon Blue 8)
07) 30 parts dispersant 1 part liquid paraffin 10 parts Next, 450 parts of a 20% vinyl chloride-vinyl acetate copolymer resin solution (10 parts resin, 20 parts toluene, 20 parts methyl ethyl ketone) was added to the above ink dispersion and stirred for about 1 hour. The mixture was dispersed using a ball mill to prepare a coating of a heat-sensitive transfer composition.
この塗剤をワイヤーバーを用いて上記ポリエステルフィ
ルムの反対面に塗布し、乾燥温度100℃で1分間乾燥
して、厚さ約5μmの熱溶融インク層を形成した。表面
を観察すると微細な多孔質状態(5〜15μ径)が観察
された。This coating material was applied to the opposite side of the polyester film using a wire bar and dried at a drying temperature of 100° C. for 1 minute to form a heat-melting ink layer with a thickness of about 5 μm. When the surface was observed, a fine porous state (5 to 15 μm in diameter) was observed.
こうして得られた転写媒体のインク層が受容体である合
成紙と対面するように重ね合わせ、転写媒体の裏面から
下記条件にて、通電パルス時間を変えて階調パターンの
画像記録を行なったところ、第5図aに示すように階調
性が優れたシアン色の画像が記録された。The ink layer of the transfer medium thus obtained was stacked so as to face synthetic paper as a receiver, and an image of a gradation pattern was recorded from the back side of the transfer medium under the following conditions by varying the energization pulse time. As shown in FIG. 5a, a cyan image with excellent gradation was recorded.
通電記録ヘッド密度: 6dOtS/mm駆動印加電圧
:25V
パルス幅: 50μsec 〜1.6m sec32階
調
実施例2
支持体、通電抵抗層形成までは、実施例1と同様で熱溶
融インク層成分だけを以下に代えた以外は全て同様にし
て階調パターンの画像記録を行なったところ、第5図の
bに示す様に階調性が優れたマゼンタ色の画像が記録さ
れた。Current-carrying recording head density: 6 dOtS/mm Driving applied voltage: 25V Pulse width: 50 μsec to 1.6 msec 32 gradations Example 2 The steps up to the formation of the support and current-carrying resistance layer were the same as in Example 1, except for the hot melt ink layer components. When an image of a gradation pattern was recorded in the same manner except for the following changes, a magenta image with excellent gradation was recorded as shown in FIG. 5b.
ラノリン脂肪酸オイル
(吉川製油製:0ES−183) 30部ラノリンワ
ックス(トルエン20%混合液)(吉川製油製:HH(
、−82> 60部着色剤(BASF製: Neoz
apon 34B) 30部分散剤
1部流動パラフィン 1
0部実施例3
実施例1および2において、熱溶融インク層成分だけを
以下に代えた以外は全て同様に行ない、階調パターンの
画像記録を行なったところ、第5図のCに示すように、
階調性が優れたイエロー色の画像が記録された。Lanolin fatty acid oil (manufactured by Yoshikawa Oil Co., Ltd.: 0ES-183) 30 parts lanolin wax (20% toluene mixture) (manufactured by Yoshikawa Oil Co., Ltd.: HH (
, -82> 60 parts Colorant (manufactured by BASF: Neoz
apon 34B) 30 part powder
1 part liquid paraffin 1
0 copies Example 3 The same procedure as in Examples 1 and 2 was carried out except that only the components of the hot-melt ink layer were changed as shown below, and when an image of a gradation pattern was recorded, the result was as shown in C in Fig. 5. ,
A yellow image with excellent gradation was recorded.
ラノリン脂肪酸オイル
(吉川製油製:LFC−50M) 30部モンチンワ
ックスS(トルエン20%混合液〉(ヘキスト製)
50部
着色剤(BASF製: Neozapon yello
w 073)25部
分散剤 1部流動パラフィ
ン 8部実施例4
実施例1〜3と同様で熱溶融インク層成分だけを下記組
成のものに代えた以外は全て同様にして、通電による階
調パターンの画像記録を行なったところ、第5図のdに
示すように階調性が優れたシアン色の画像が記録された
。Lanolin fatty acid oil (manufactured by Yoshikawa Oil Co., Ltd.: LFC-50M) 30 parts Montin wax S (20% toluene mixture) (manufactured by Hoechst)
50 parts Colorant (manufactured by BASF: Neozapon yellow
w 073) 25 parts dispersant 1 part liquid paraffin 8 parts Example 4 Same as Examples 1 to 3 except that only the components of the hot-melt ink layer were replaced with those of the following composition. When an image was recorded, a cyan image with excellent gradation was recorded as shown in d of FIG.
ラノリン脂肪酸オイル
(OES−183、古川製油製) 30部ラノリンワ
ックス(トルエン20%混合液)(FPG−1、吉川製
油製) 60部着色剤(Neozapon Blue
807、BASF製)90部
階調制御剤=2,7−ビス[2−ヒドロキシ−3−(2
−クロルフェニルカルバモイル)ナフタレン−1−イル
アゾ1−9−フルオレノン20部
分散剤 1部流動パラフィ
ン 9部比較例1
実施例1〜3と同様に、支持体、通電抵抗層までは全く
同様で、熱溶融インク層成分を下記の処方とし、3本ロ
ールミルで分散して、ホットメルト法で約5μ厚の熱溶
融インク層を形成した。Lanolin fatty acid oil (OES-183, manufactured by Furukawa Oil Co., Ltd.) 30 parts Lanolin wax (20% toluene mixture) (FPG-1, manufactured by Yoshikawa Oil Co., Ltd.) 60 parts Colorant (Neozapon Blue)
807, manufactured by BASF) 90 parts Tone control agent = 2,7-bis[2-hydroxy-3-(2
-Chlorphenylcarbamoyl)naphthalen-1-ylazo1-9-fluorenone 20 parts Dispersant 1 part Liquid paraffin 9 parts Comparative Example 1 As in Examples 1 to 3, the support and current-carrying resistance layer are exactly the same, and the heat melting The components of the ink layer were prepared as follows, and dispersed in a three-roll mill to form a heat-melting ink layer having a thickness of approximately 5 μm using a hot-melt method.
フタロシアニン顔料 20部パラフィンワ
ックス 20部酸化ワックス
40部エチレン・酢ビ共重合体 20
部ステアリン酸 3部この表面は
ほとんど微細な多孔質状態は観察されなかった。Phthalocyanine pigment 20 parts Paraffin wax 20 parts Oxidized wax
40 parts ethylene/vinyl acetate copolymer 20
Part stearic acid 3 parts Almost no fine porous state was observed on this surface.
同様にして階調パターンの画像記録を行なつたところ、
第5図のXに示すように階調性の劣る画像が記録された
。When an image of a gradation pattern was recorded in the same way,
As shown by X in FIG. 5, an image with poor gradation was recorded.
比較例2
実施例1の多孔質を形成する塩ビー酢ビ共重合体の樹脂
溶液を加えずに、その他は全く同様にしてワイヤーバー
を用いてコーティングして熱溶融インク層を形成した。Comparative Example 2 A hot-melt ink layer was formed by coating using a wire bar in the same manner as in Example 1, except that the resin solution of the vinyl chloride-vinyl acetate copolymer that forms the porous structure was not added.
同様に通電記録による階調パターンを記録したところ、
第5図のyに示すように階調性の劣る画像が記録された
。Similarly, when we recorded the gradation pattern by energization recording, we found that
As shown in y in FIG. 5, an image with poor gradation was recorded.
実施例5
m−フェニレンテレフタルアミド 9部カーボンブラッ
ク(ケッチェンブラック、日本イージー社製) 1部
塩化カルシウム 5部N−メチル−
2−ピロリドン 85部以上の混合物をボールミル
で48時間分散したものを、ガラス板上にギャップ20
0μ■のブレードを用いて流延塗布し、110℃の乾燥
機中で1時間乾燥した後、約5℃の冷水中に1分間浸漬
しガラス板上から剥離した。次いで約20℃の流水中で
水洗してから湿潤状態において、縦横それぞれの方向に
2倍ずつ延伸し、さらに300°Cで10分間熱処理を
行なって、厚さ約20μmの中抵抗支持体を1qだ。Example 5 m-Phenylene terephthalamide 9 parts Carbon black (Ketjen black, manufactured by Japan Easy Co., Ltd.) 1 part Calcium chloride 5 parts N-methyl-
A mixture containing 85 parts or more of 2-pyrrolidone was dispersed in a ball mill for 48 hours, and then placed on a glass plate with a gap of 20
The coating was cast using a 0 μm blade, dried in a dryer at 110° C. for 1 hour, and then immersed in cold water at about 5° C. for 1 minute to peel off from the glass plate. Next, after washing in running water at about 20°C, in a wet state, it was stretched twice in each direction, lengthwise and horizontally, and then heat-treated at 300°C for 10 minutes to form a medium resistance support with a thickness of about 20μm. is.
続いて下記の抵抗層成分混合液を約60°Cの恒温槽の
中でボールミルで約24時量子分分散させ、その塗剤を
ワイヤーバーを用いて上記支持体表面に塗布、乾燥温度
100℃で1分間乾燥して、厚さ約4μmの通電抵抗層
を形成した。Next, the following resistance layer component mixture was dispersed in a ball mill for about 24 hours in a constant temperature bath at about 60°C, and the coating material was applied to the surface of the support using a wire bar, and the drying temperature was 100°C. This was dried for 1 minute to form a current-carrying resistance layer with a thickness of about 4 μm.
カーボンブラック(Printex 90 :コロンビ
アカーボン製)30部
ポリアミド樹脂(0M4000:東し製)80部
メタノール 200部エタノール
200部次いで実施例1と同様の
熱溶融インク層を形成し、実施例1と同様の画像記録を
行なったところ、実施例1と同様の階調性が優れたシア
ン色の画像が記録された。Carbon black (Printex 90: manufactured by Columbia Carbon) 30 parts Polyamide resin (0M4000: manufactured by Toshi) 80 parts Methanol 200 parts Ethanol
200 copies Then, a heat-melting ink layer similar to that in Example 1 was formed and an image was recorded in the same manner as in Example 1. As a result, a cyan image with excellent gradation similar to that in Example 1 was recorded. .
実施例6
中抵抗支持体、通電抵抗層形成までは実施例5と同様で
、以下は実施例2と同様にして、階調パターンの画像記
録を行なったところ、実施例2と同様の階調性が優れた
マゼンタ色の画像が記録された。Example 6 The steps up to the formation of the medium resistance support and the current carrying resistance layer were the same as in Example 5, and the following steps were carried out in the same manner as in Example 2. When an image of a gradation pattern was recorded, the same gradation as in Example 2 was obtained. A magenta image with excellent quality was recorded.
実施例7
熱溶融インク層成分だけを実施例3と同じものに代えた
以外は全て実施例5および実施例6と同様にして、階調
パターンの画像記録を行なったところ、同様の階調性が
優れたイエロー色の画像が記録された。Example 7 Images of gradation patterns were recorded in the same manner as in Examples 5 and 6 except that only the components of the hot melt ink layer were replaced with the same ones as in Example 3. Similar gradation properties were obtained. A yellow image with excellent color was recorded.
実施例8
支持体上番こ通電抵抗層として10’ mmHgの真空
中でA1を蒸着して、約50003.の薄膜層を設けて
熱溶融インク層を設けた以外は実施例5〜7と同様にし
て、通電による階調パターンの画像記録を行なったとこ
ろ実施例4と同様の階調性が優れたシアン色の画像が記
録された。Example 8 A1 was deposited as a current carrying resistance layer on the support in a vacuum of 10' mmHg to a thickness of about 50,003 mm. Images of gradation patterns were recorded by energization in the same manner as in Examples 5 to 7 except that a thin film layer was provided and a heat-melting ink layer was provided. A color image was recorded.
比較例3
実施例5〜7の熱溶融インク層成分を比較例1に同じ組
成に代えて階調パターンの画像記録を行なったところ、
比較例1と同様の階調性の劣る画像が記録された。Comparative Example 3 When an image recording of a gradation pattern was performed by replacing the hot melt ink layer components of Examples 5 to 7 with the same composition as in Comparative Example 1,
An image with poor gradation similar to Comparative Example 1 was recorded.
比較例4
実施例5の多孔質を形成する塩ビー酢ビ共重合体の樹脂
溶液を加えずに階調パターンを記録したところ、比較例
2と同様の階調性に劣る画像が記録された。Comparative Example 4 When a gradation pattern was recorded without adding the resin solution of vinyl chloride-vinyl acetate copolymer forming the porous structure of Example 5, an image with poor gradation similar to Comparative Example 2 was recorded. .
実施例9
下記の抵抗層成分混合液を約60℃の恒温槽の中でボー
ルミルで約24時量子分分散させ、実施例1と同様にし
て通電抵抗層を形成した。Example 9 A current-carrying resistance layer was formed in the same manner as in Example 1 by subjecting the following resistance layer component mixture to quantum dispersion for about 24 hours using a ball mill in a constant temperature bath at about 60°C.
カーボンブラック(Printex 90゜コロンビア
カーボン製) 30部
ポリアミド樹脂 80部メタノール
400部次いで実施例1と同じ感熱
転写組成物の塗剤をつくり、この塗剤をワイヤーバーを
用いて上記ポリエステルフィルムの通電抵抗層を設けた
面に塗布し、乾燥温度100℃で1分間乾燥して厚さ約
5μmの熱溶融インク層を形成した。Carbon black (Printex 90° manufactured by Columbia Carbon) 30 parts Polyamide resin 80 parts Methanol
400 parts of the same heat-sensitive transfer composition as in Example 1 was then prepared, and this coating was applied to the surface of the polyester film on which the current carrying resistance layer was provided using a wire bar, and dried for 1 minute at a drying temperature of 100°C. A heat-melting ink layer having a thickness of approximately 5 μm was formed.
こうして得た転写媒体を実施例1と同様にしで画像記録
を行なったところ、実施例1と同様の結果を得た。When an image was recorded on the thus obtained transfer medium in the same manner as in Example 1, the same results as in Example 1 were obtained.
実施例10
熱溶融インク層成分を実施例2と同じものに代えた以外
は実施例9と同様にしたところ、実施例2と同様の階調
性が優れたマゼンタ色の画像が記録された。Example 10 Example 9 was repeated except that the components of the hot-melt ink layer were replaced with the same components as in Example 2. A magenta image with excellent gradation similar to Example 2 was recorded.
実施例11
熱溶融インク層成分を実施例3と同じものに代えた以外
は実施例9.10と同様にしたところ、実施例3と同様
の階調性が優れたイエロー色の画像が記録された。Example 11 The same procedure as Example 9.10 was carried out except that the components of the hot-melt ink layer were replaced with the same ones as in Example 3. A yellow image with excellent gradation similar to that in Example 3 was recorded. Ta.
実施例12
熱溶融インク層成分を実施例4と同じものに代えた以外
は実施例9〜11と同様にしたところ、実施例3と同様
の階調性が優れたシアン色の画像が記録された。Example 12 The same procedures as Examples 9 to 11 were carried out except that the components of the hot-melt ink layer were replaced with the same ones as in Example 4. A cyan image with excellent gradation similar to that in Example 3 was recorded. Ta.
比較例5
実施例9〜11の熱溶融インク層成分を比較例1と同じ
組成に代えて階調パターンの画像記録を行なったところ
比較例1と同様の階調性の劣る画像が記録された。Comparative Example 5 When an image of a gradation pattern was recorded by replacing the hot melt ink layer components of Examples 9 to 11 with the same composition as Comparative Example 1, an image with poor gradation similar to Comparative Example 1 was recorded. .
比較例6
実施例9の多孔質を形成する塩ビー酢ビ共重合体の樹脂
溶液を加えずに階調パターンを記録したところ、比較例
2と同様の階調性の劣る画像が得られた。Comparative Example 6 When a gradation pattern was recorded without adding the resin solution of the vinyl chloride-vinyl acetate copolymer that forms the porosity of Example 9, an image with poor gradation similar to Comparative Example 2 was obtained. .
実施例13
実施例5の中抵抗支持体におけるカーボンブラック1部
の代わりに銅粉10部に代えて通電層を得た。ついで実
施例5と同じ通電抵抗層を形成した。Example 13 A current-carrying layer was obtained by replacing 1 part of carbon black in the medium resistance support of Example 5 with 10 parts of copper powder. Then, the same current carrying resistance layer as in Example 5 was formed.
ついで下記処方の混合液を約80℃の恒温槽の中で十分
分散させ、この塗剤をワイヤーバーを用いて上記通電抵
抗層上に塗布し、乾燥温度100℃で約3分間乾燥して
約2μの導電層を形成した。Next, a mixture of the following formulation was sufficiently dispersed in a constant temperature bath at about 80°C, and this paint was applied onto the current carrying resistance layer using a wire bar, and dried at a drying temperature of 100°C for about 3 minutes to form a coating of about 80°C. A 2μ thick conductive layer was formed.
カーボンブラック(Printex 90゜コロンビア
カーボン製)25部
ポリビニルアルコール樹脂 80部水
500部ついで実施例5
と同じ熱溶融インク層を形成した。Carbon black (Printex 90° manufactured by Columbia Carbon) 25 parts Polyvinyl alcohol resin 80 parts Water
500 copies then Example 5
The same hot-melt ink layer was formed.
得られた転写媒体を実施例5と同様に画像記録したとこ
ろ、実施例5と同様に階調性が優れたシアン色の画像が
記録された。When an image was recorded on the obtained transfer medium in the same manner as in Example 5, a cyan image with excellent gradation was recorded as in Example 5.
実施例14
熱溶融インク層を実施例2と同じとし、他は実施例13
と同様にして、階調パターンの画像記録を行なったとこ
ろ、実施例2と同様の階調性が優れたマゼンタ色の画像
が形成された。Example 14 The heat-melting ink layer was the same as in Example 2, and the others were as in Example 13.
When an image of a gradation pattern was recorded in the same manner as in Example 2, a magenta image with excellent gradation properties similar to that of Example 2 was formed.
実施例15
熱溶融インク層成分だけを実施例3と同じものに代えた
以外はすべて実施例13と同様にして階調パターンの画
像記録を行なったところ、同様の階調性が優れたイエロ
ー色の画像が記録された。Example 15 When an image of a gradation pattern was recorded in the same manner as in Example 13 except that only the components of the heat-melting ink layer were replaced with the same ones as in Example 3, a yellow color with similar excellent gradation properties was obtained. images were recorded.
実施例16
熱溶融インク層成分だけを実施例4と同じものに代えた
以外は実施例13と同様にして画像記録したところ、実
施例4と同様に階調性が優れたシアン色の画像が記録さ
れた。Example 16 An image was recorded in the same manner as in Example 13 except that only the components of the hot melt ink layer were replaced with the same ones as in Example 4. As in Example 4, a cyan image with excellent gradation was obtained. recorded.
比較例7
実施例14〜16の熱溶融インク層成分を比較例1と同
じ組成に代えて階調パターンの画像記録を行なったとこ
ろ、比較例1と同様の階調性の劣る画像が記録された。Comparative Example 7 When an image of a gradation pattern was recorded by replacing the hot melt ink layer components of Examples 14 to 16 with the same composition as Comparative Example 1, an image with poor gradation similar to Comparative Example 1 was recorded. Ta.
比較例8
実施例14〜16の熱溶融インク層成分を比較例2と同
じ組成に代えて階調パターンの画像記録を行なったとこ
ろ、比較例2と同様の階調性の劣る画像が1qられた。Comparative Example 8 When an image of a gradation pattern was recorded by replacing the hot melt ink layer components of Examples 14 to 16 with the same composition as Comparative Example 2, an image with poor gradation similar to Comparative Example 2 was obtained. Ta.
L効 果]
以上の説明から明らかなようにこの発明の通電感熱転写
記録媒体は通電パルス幅の大小に応じて多孔質組織の間
からインクかにじみ出て、受容シート面に転移するので
、転写の際の通電印加パルス幅を制御することによって
、階調表現の優れた(階調再現の広い)転写画像を得る
ことができ、またその画像が保存性がよく、いろいろの
染料の選択によってフルカラー画像を得ることもできる
。[L effect] As is clear from the above explanation, in the current-applying thermal transfer recording medium of the present invention, ink oozes out from between the porous structures and transfers to the receiving sheet surface depending on the magnitude of the current-applying pulse width, so that the transfer is effected. By controlling the pulse width of the current applied at the time of application, it is possible to obtain transferred images with excellent gradation expression (wide gradation reproduction), and the images have good storage stability. You can also get
第1図ないし第3図は本発明の各実施例の説明図、第4
図はその使用態様の説明図、第5図は実施例と比較例の
階調パターンを示すグラフである。
1・・・支持体、1゛・・・中抵抗支持体、2・・・通
電抵抗層、3・・・インク層、4・・・微細多孔質組織
、5・・・熱溶融インク成分、6・・・通電層、7・・
・受容シート、8・・・通電ヘッド。
特許出願人 株式会社リ コ −
代理人 弁理士 小 松 秀 岳
代理人 弁理士 旭 宏
5」二J斐示弓プ扁シ支ジ1
第5図
5 10 15 20 25 ℃η階 別Figures 1 to 3 are explanatory diagrams of each embodiment of the present invention, and Figure 4 is an illustration of each embodiment of the present invention.
The figure is an explanatory diagram of its usage, and FIG. 5 is a graph showing gradation patterns of an example and a comparative example. DESCRIPTION OF SYMBOLS 1... Support body, 1'... Medium resistance support body, 2... Current carrying resistance layer, 3... Ink layer, 4... Fine porous structure, 5... Hot melt ink component, 6... Current carrying layer, 7...
- Receptor sheet, 8... energizing head. Patent Applicant Ricoh Co., Ltd. - Agent Patent Attorney Hide Komatsu Agent Patent Attorney Hiroshi Asahi
Claims (1)
層を有する記録媒体において、該インク層は樹脂からな
る微細多孔質組織中に常温では固体の熱溶融性物質と着
色剤とを主成分とする熱溶融インク成分を含有した構造
からなることを特徴とする通電感熱転写記録媒体。In a recording medium that has a support layer and an ink layer that generate Joule heat when energized, the ink layer has a microporous structure made of resin that contains a heat-melting substance that is solid at room temperature and a colorant as its main components. An electrically conductive thermal transfer recording medium characterized by having a structure containing a molten ink component.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61120971A JPS62278089A (en) | 1986-05-28 | 1986-05-28 | Electothermal transfer recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61120971A JPS62278089A (en) | 1986-05-28 | 1986-05-28 | Electothermal transfer recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62278089A true JPS62278089A (en) | 1987-12-02 |
Family
ID=14799558
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61120971A Pending JPS62278089A (en) | 1986-05-28 | 1986-05-28 | Electothermal transfer recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62278089A (en) |
-
1986
- 1986-05-28 JP JP61120971A patent/JPS62278089A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS58183297A (en) | Multiple heat transfer sheet for gradation recording and preparation thereof | |
JPS62278089A (en) | Electothermal transfer recording medium | |
JPS6145552B2 (en) | ||
JPS62284788A (en) | Transfer recording medium | |
JPH01135687A (en) | Thermal transfer recording medium | |
JP2635552B2 (en) | Transfer recording medium | |
JPH0197684A (en) | Thermosensitive recording paper | |
JPS6353094A (en) | Thermal transfer recording medium | |
JPS62124981A (en) | Thermal transfer recording medium | |
JPH0197686A (en) | Thermosensitive recording paper | |
JPH01135688A (en) | Thermal transfer recording medium | |
JPS6227186A (en) | Thermal transfer recording medium | |
JPH01133785A (en) | Thermal transfer recording medium | |
JPH01208189A (en) | Thermal transfer recording medium | |
JPH0197685A (en) | Thermosensitive recording paper | |
JPS62270384A (en) | Transfer recording medium | |
JPS63126791A (en) | Thermal transfer recording medium | |
JPS61199995A (en) | Thermal transfer recording medium | |
JPH01306286A (en) | Thermal transfer recording medium | |
JPS63296985A (en) | Thermal transfer recording medium | |
JPS62121090A (en) | Thermal transfer recording medium | |
JPS6230081A (en) | Thermal sensitive transfer recording medium | |
JPS6362786A (en) | Transfer recording medium | |
JPS6253882A (en) | Thermal transfer recording medium | |
JPH01120387A (en) | Thermosensitive transfer recording medium |