JPS6282085A - Thermal transfer recording medium - Google Patents
Thermal transfer recording mediumInfo
- Publication number
- JPS6282085A JPS6282085A JP60224046A JP22404685A JPS6282085A JP S6282085 A JPS6282085 A JP S6282085A JP 60224046 A JP60224046 A JP 60224046A JP 22404685 A JP22404685 A JP 22404685A JP S6282085 A JPS6282085 A JP S6282085A
- Authority
- JP
- Japan
- Prior art keywords
- ink layer
- thermal transfer
- transfer recording
- paper
- aqueous emulsion
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000012546 transfer Methods 0.000 title claims abstract description 40
- 239000000839 emulsion Substances 0.000 claims abstract description 24
- 239000000126 substance Substances 0.000 claims abstract description 15
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 7
- 238000002844 melting Methods 0.000 claims description 5
- 238000007639 printing Methods 0.000 abstract description 15
- 239000000853 adhesive Substances 0.000 abstract description 8
- 230000001070 adhesive effect Effects 0.000 abstract description 8
- 229920000642 polymer Polymers 0.000 abstract description 3
- 239000002904 solvent Substances 0.000 abstract description 3
- 230000016615 flocculation Effects 0.000 abstract 1
- 238000005189 flocculation Methods 0.000 abstract 1
- 239000000976 ink Substances 0.000 description 43
- 238000000034 method Methods 0.000 description 13
- -1 on a support Substances 0.000 description 13
- 239000001993 wax Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 6
- 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 5
- 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 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 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 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 230000000903 blocking effect Effects 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 238000005562 fading Methods 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 230000000740 bleeding effect Effects 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- KEMQGTRYUADPNZ-UHFFFAOYSA-N heptadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(O)=O KEMQGTRYUADPNZ-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical class CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 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
- 239000012860 organic pigment Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- REZQBEBOWJAQKS-UHFFFAOYSA-N triacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO REZQBEBOWJAQKS-UHFFFAOYSA-N 0.000 description 2
- KMEHEQFDWWYZIO-UHFFFAOYSA-N triacontyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC KMEHEQFDWWYZIO-UHFFFAOYSA-N 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- JDIOBXDRZVLCFV-UHFFFAOYSA-N 2-oxopyran-3-carbaldehyde Chemical compound O=CC1=CC=COC1=O JDIOBXDRZVLCFV-UHFFFAOYSA-N 0.000 description 1
- FEIQOMCWGDNMHM-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid Chemical group OC(=O)C=CC=CC1=CC=CC=C1 FEIQOMCWGDNMHM-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241000234435 Lilium Species 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000002789 Panax ginseng Nutrition 0.000 description 1
- 240000004371 Panax ginseng Species 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
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-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
- 239000012164 animal wax Substances 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- CJOBVZJTOIVNNF-UHFFFAOYSA-N cadmium sulfide Chemical compound [Cd]=S CJOBVZJTOIVNNF-UHFFFAOYSA-N 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003984 copper intrauterine device Substances 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- VPNOHCYAOXWMAR-UHFFFAOYSA-N docosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCN VPNOHCYAOXWMAR-UHFFFAOYSA-N 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 description 1
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000010365 information processing Effects 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000012184 mineral wax Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- 125000001802 myricyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 238000000614 phase inversion technique Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920006122 polyamide resin 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
- 229920001721 polyimide Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
- 229960003351 prussian blue Drugs 0.000 description 1
- 239000013225 prussian blue Substances 0.000 description 1
- 238000001454 recorded image Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001846 repelling effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- 238000001132 ultrasonic dispersion Methods 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 239000002023 wood Substances 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
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
- B41M5/423—Intermediate, backcoat, or covering layers characterised by non-macromolecular compounds, e.g. waxes
-
- 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
- B41M5/392—Additives, other than colour forming substances, dyes or pigments, e.g. sensitisers, transfer promoting agents
-
- 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
- B41M5/392—Additives, other than colour forming substances, dyes or pigments, e.g. sensitisers, transfer promoting agents
- B41M5/395—Macromolecular additives, e.g. binders
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- 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■〕
本発明はva熱熱転写記録体体関し、詳しくは表面平滑
性の悪いラフペーパーに対しても良質な印字を与える感
熱転写記録媒体に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application (2)] The present invention relates to a VA thermal transfer recording medium, and more particularly to a thermal transfer recording medium that provides good quality printing even on rough paper with poor surface smoothness.
近年、情報処理システムのr1n発は目覚ましく、これ
に伴ないそれぞれのシステムに適した記録方法及び装置
も開発、採用されている。この中でも感熱記録方法が、
装での軽量かつコンパクト、無藝音、優れた操作性、保
守性等の点から広く使用されている。In recent years, there has been a remarkable increase in R1N information processing systems, and with this, recording methods and devices suitable for each system have been developed and adopted. Among these, the thermal recording method is
It is widely used because it is lightweight, compact, silent, and has excellent operability and maintainability.
しかし、感熱記録方法に用いられる記録紙の中、通常の
感熱記録紙は発色剤と顕色剤を含む発色型であるため高
価であり、また記録紙が熱や有機溶剤により容易に発色
したり、記録像が比較的短時間に退色するなど保存性の
面でも欠点があった。However, among the recording papers used in thermal recording methods, ordinary thermal recording paper is expensive because it is a coloring type that contains a color former and a color developer, and the recording paper easily develops color due to heat or organic solvents. However, there were also drawbacks in terms of storage stability, such as the recorded image fading in a relatively short period of time.
上記欠点を改善するものとして最近特に注目されている
のが感熱転写記録方法である。A thermal transfer recording method has recently attracted particular attention as a method for improving the above-mentioned drawbacks.
この感熱転写記録方法は、通常シート状の支持体上に、
熱溶融性物質中に着色剤を分散させた熱溶融性インク層
を有する感熱転写記録媒体を用い、該インク層を被転写
謀体(一般には祇)に重ねた状態で感熱転写記録媒体の
支持体側からサーマルヘッドにより加熱し、溶融したイ
ンク層を被転写u体に転写することで、加熱形状に応じ
たインク像を形成させるものである。この方法により%
普通紙、の記録も可能となり、前記感熱記録紙0欠点も
解決された。In this thermal transfer recording method, normally, on a sheet-like support,
Using a heat-sensitive transfer recording medium having a heat-fusible ink layer in which a colorant is dispersed in a heat-fusible substance, the heat-sensitive transfer recording medium is supported with the ink layer superimposed on a transfer target (generally a layer). By heating with a thermal head from the body side and transferring the melted ink layer to the transfer target U body, an ink image corresponding to the heated shape is formed. By this method %
It has also become possible to record on plain paper, and the drawbacks of the above-mentioned thermal recording paper have been solved.
L tJ′L rj″(ら・0の感熱転写記録方法にも
被転写媒体の表面平滑度により印字品質が左右されると
いう問題がある。![1ち、平滑性の高い被転写媒体へ
は良好な印字が行われるが、平滑性の低い被転写媒体を
用いた場合には著しく印字品質が低下する。これは最も
典型的な被転写媒体である紙を使用する場合に特に障害
となる。即ち、平滑性の高い紙はむしろ特殊であり、通
常の紙は繊維の絡み合いにより、がなりの凹凸を有して
おり、ベック平滑度10秒程度のラフペーパーにおいて
は凸部上端から凹部下端迄が10 am以上の部分があ
る。L tJ'L rj'' (The thermal transfer recording method of La.0 also has the problem that the print quality is affected by the surface smoothness of the transfer medium. Although good printing is achieved, the print quality is significantly reduced when a transfer medium with low smoothness is used. This is a particular problem when using paper, which is the most typical transfer medium. In other words, paper with high smoothness is rather special; ordinary paper has unevenness due to intertwining of fibers, and rough paper with a Bekk smoothness of about 10 seconds has a rough surface from the top of the convex part to the bottom of the concave part. There are parts where the distance is 10 am or more.
このような紙を用いて熱転写による印字を行うと、印字
濃度が低かったり、印字の一部が欠けたりして印字品質
を大きく劣化させる。When thermal transfer printing is performed using such paper, the print density is low or parts of the print are missing, resulting in a significant deterioration in print quality.
この熱転写性を向上する目的で、熱溶融性インク層の熱
溶融性物質に融点の低いワックス類の使用が考えられる
が、溶融性は上昇し紙への浸6が進み紙との実質的な接
着面積は大きくなるが、インク層の凝集力と共にインク
層と紙との接着力が低下するため十分な効果が得られず
、却ってインク層が比較的低温でも粘着性を帯び、保存
性の低下ならびに印字の滲み、非印字部の汚れ(地汚れ
)等の障害を与える。またインク層の紙との接着力は本
質的に弱いため接着面積を、より大きくするためにはイ
ンク層の膜厚を厚くしなければならず、印字の滲みの増
加やサーマルヘッドへの熱供給9も大きくする8娶があ
り印字速度の低下を招く。In order to improve this heat transferability, it is possible to use waxes with a low melting point as the heat-fusible substance in the heat-fusible ink layer, but the meltability increases and immersion into the paper progresses, resulting in a substantial bond between the paper and the paper. Although the adhesion area becomes larger, the adhesive strength between the ink layer and the paper decreases as well as the cohesive force of the ink layer, so a sufficient effect cannot be obtained, and the ink layer becomes sticky even at relatively low temperatures, resulting in a decrease in storage stability. It also causes problems such as blurring of printed characters and staining of non-printed areas (background stains). In addition, the adhesive strength of the ink layer to paper is inherently weak, so in order to increase the adhesion area, the thickness of the ink layer must be increased. There is also an 8-bit which increases the size of 9, which causes a decrease in printing speed.
従って、上記の欠点を改良し、表面平滑性の悪いラフペ
ーパーに対しても良好な印字を与えることができる感熱
転写記録媒体の開発が要望されている。Therefore, there is a need for the development of a thermal transfer recording medium that can improve the above-mentioned drawbacks and can provide good printing even on rough paper with poor surface smoothness.
本発明の目的は、表面平滑性の悪いラフペーパーに対し
ても良好な印字品質で印字することができる感熱転写記
録媒体を提供することにある。An object of the present invention is to provide a thermal transfer recording medium that can print with good print quality even on rough paper with poor surface smoothness.
本発明者らはインク層の接着力と凝集力との関係につい
て鋭意研究を絖けた結果、支持体上に熱溶融性物質の水
性エマルジ曹ン3含有する層と、その上に熱可堕性樹脂
の水性エマルジ嘗ンを含有するインク層を少なくとも一
層有する感熱転写記録媒体の前記インク層の膜厚f2a
m以下とすることにより上記目的が達成されることを見
出し、本発明をなすに至った。The present inventors conducted intensive research on the relationship between the adhesive force and cohesive force of the ink layer, and found that a layer containing water-based emulsion carbon 3, a heat-melting substance, on a support, and a layer containing a heat-meltable substance, a thermo-degradable Thickness f2a of the ink layer of a thermal transfer recording medium having at least one ink layer containing an aqueous emulsion of a resin
The inventors have discovered that the above object can be achieved by setting it to m or less, and have accomplished the present invention.
以下、本発明をより具体的に説明する。The present invention will be explained in more detail below.
インクばはエネルギー印加後、感熱転写記録媒体と紙が
実質的に離れる時、紙との接着力が強く支持体との接着
力が弱く、また凝集力もある程度弱い方が好ましい。し
かし、インク層の凝集力は一般に接着力と相関があり、
両者を満足させるのは回想である。発明者らはインクr
:!1fr:水性エマルジョンで形成した場合に溶S系
で形成した場合に比へ、インクDと祇との接着力は多少
低下するが、疑集力もイ氏下して、熱転写系において:
=極めて有利であることひ見出した。また、ポリマーを
主成分として溶媒系で形成したインクでは印字された文
字のエツジ部分にヒゲ秋の糸引き現争が起こり易いが、
これもエマルジ繋ン系の方が少ない。更にブロッキング
を生ずる温度も高くなることが刈った。When the thermal transfer recording medium and the paper are substantially separated after energy is applied, the ink layer preferably has a strong adhesive force with the paper, a weak adhesive force with the support, and a somewhat weak cohesive force. However, the cohesive force of the ink layer is generally correlated with the adhesive force;
Reminiscence is what satisfies both parties. The inventors ink r
:! 1fr: When formed with an aqueous emulsion, the adhesion force between Ink D and Ink is somewhat lower than when formed with a molten S system, but the binding force is also lowered, and in a thermal transfer system:
= I discovered that it is extremely advantageous. In addition, with solvent-based inks containing polymer as the main component, threading is likely to occur at the edges of printed characters.
This is also less in the emulsion connection system. Furthermore, the temperature at which blocking occurs also increases.
また、インク層の凝集力が強くても、その膜厚を薄くす
ると凝集力だけ2弱くした時と同じ効果が得られること
、その上限が 2μmであることも見出した。We also discovered that even if the ink layer has a strong cohesive force, if the thickness of the ink layer is reduced, the same effect as when the cohesive force is made weaker by 2 can be obtained, and that the upper limit is 2 μm.
熱溶融性物質の水性エマルジ3ン3含vfる居(本出願
においてはインク層に対して下、芒と呼ぶ)はインク層
と支持体との接着力分調節する役割3果す。部も、冷時
においては、インク層の膜付性、V!強度等の機械的取
扱い性ご琲持し、加熱時にインクだとの接着力な弱める
ものが好ましい。下1層はインク層と共に記録紙に転写
させてもよいが、その場合には下層の;フ集力とインク
層の凝集力は加算される形となり、インク、苦と記り祇
の接・打力は更に強いことが要求されるので下層とイン
クワの間で剥離させるのが好ましい。The aqueous emulsion containing the heat-fusible material (referred to as the awn in this application with respect to the ink layer) plays a role in adjusting the adhesion force between the ink layer and the support. Also, when cold, the film adhesion of the ink layer, V! It is preferable to use a material that has good mechanical handling properties such as strength, and weakens the adhesion to ink when heated. The lower layer may be transferred to the recording paper together with the ink layer, but in that case, the cohesive force of the lower layer and the cohesive force of the ink layer will be added, and the ink will be transferred to the recording paper together with the ink layer. Since stronger striking force is required, it is preferable to separate the ink between the lower layer and the ink.
下層の膜厚は薄くてもよいが、インク音より厚い時に特
に良質な印字が得られる。これはインク層が巧いと1紙
との実質的な!2着断面積凹凸のため少qくなるが、下
層が厚いことにより、この部分で紙の凹凸を吸収して、
インクDと紙との実質的接着面積を増大させるためと考
えられる。Tmの膜厚としては0.5〜5μm である
ことが好ましい。Although the thickness of the lower layer may be thin, particularly good quality printing can be obtained when it is thicker than the ink layer. If the ink layer is good, this is practically the same as one paper! 2nd place The cross-sectional area will be uneven, so it will be less q, but because the bottom layer is thick, this part will absorb the unevenness of the paper,
This is thought to be because the substantial adhesion area between the ink D and the paper is increased. The thickness of Tm is preferably 0.5 to 5 μm.
本発明のTmには熱溶融性物質の水性エマルジョンが用
いられる。熱溶融性物質は融点(榔本MPJ−2型によ
る測定(Ii ) が40〜150℃の固体または半
固体状物質であることが好ましい。具体例としては、例
えばカルナバロウ、木ロウ、オウリキエリーロウ、ニス
パルロウ等の植物ロウ、蜜ロウ、昆虫ロウ、セラ7クロ
ウ、諒ロウ等の動物ロウ、パラフィンワックス、マイク
ロクリスタリンワックス、ポリエチレンワックス、エス
テルワックス、ヒワフクス等の石油ロウ、モンタンロウ
、オシケライト、モンタン等の鉱物ロウ等のワックス類
の他に;パルミチン酸、ステアリン酸、マルガリン酸、
ベヘン酸等の高級脂肪酸;ハルミ千ルアルフール、ステ
アリルアルコール、ベヘニルアルコール、マルガニルア
ルコール、ミリシルアルコール、エイコサ/−ル等の高
級アルコール;パルミチン酸七千ル、パルミチン酸ミリ
シル、ステアリン階上チル、ステアリン酸ミリシル等の
高級脂肪酸エステルニア七ドアミド、プロピオン鼓アミ
ド、パルミチン酸アミド、ステアリン酸アミド、アミド
ワックス等のアミド類;エステルガム、ロジンマレイン
aim、ロジンフェノールtaU、 水添ロジン等のロ
ジン誘導体;フェノール樹脂、テルペン樹脂、シクロペ
ンタジェンjBI 詣、芳N fl、 m砺詣等の快化
点50−150℃の高分子化合物;ステアリル7ミン、
ベヘニルアミン、パルミ千ルアミン等の高級アミンWi
等が挙げられ、これらは単独でmいられてもよいし併用
してもよい。An aqueous emulsion of a thermofusible substance is used as the Tm of the present invention. The heat-melting substance is preferably a solid or semi-solid substance with a melting point (measured by Sakemoto MPJ-2 model (Ii)) of 40 to 150°C.Specific examples include carnauba wax, wood wax, and ouriquerie. Wax, vegetable wax such as Nispar wax, beeswax, insect wax, animal wax such as Cera 7 Claw, lily wax, paraffin wax, microcrystalline wax, polyethylene wax, ester wax, petroleum wax such as Hiwafukusu, montan wax, osichelite, montan, etc. In addition to waxes such as mineral wax; palmitic acid, stearic acid, margaric acid,
Higher fatty acids such as behenic acid; higher alcohols such as haloalfur, stearyl alcohol, behenyl alcohol, marganyl alcohol, myricyl alcohol, and eicosa/-al; 7000 palmitate, myricyl palmitate, stearic acid, stearic acid Amides such as higher fatty acid ester nia-heptamide such as myricyl, propionic acid amide, palmitic acid amide, stearic acid amide, amide wax; rosin derivatives such as ester gum, rosin maleic acid aim, rosin phenol taU, hydrogenated rosin; phenolic resin , terpene resin, cyclopentadiene, polymer compounds with a recovery point of 50-150°C, such as cyclopentadiene, cyclopentadiene,
Higher amines Wi such as behenylamine and palmythylamine
These may be used alone or in combination.
熱溶融性物質を水性エマルジョンとするには、乳化剤を
含む系で、転相法、高圧乳化法、超音波分散法等の既存
の方法で水中に乳化させればよい。In order to form a hot-melt substance into an aqueous emulsion, it may be emulsified in water using an existing method such as a phase inversion method, a high-pressure emulsification method, or an ultrasonic dispersion method using a system containing an emulsifier.
乳化剤としては、/ニオン性、アニオン性、カチオン性
、両性のいずれでもよい。また、支持体との冷時におけ
る膜付き性等を得るために熱溶融性物質の水性エマルジ
ョンに熱可塑性樹脂の水性エマルジョンを適宜混合して
用いてもよい。The emulsifier may be any of anionic, anionic, cationic, and amphoteric emulsifiers. Further, in order to obtain the ability to form a film on the support when cold, etc., an aqueous emulsion of a thermoplastic resin may be appropriately mixed with an aqueous emulsion of a thermofusible substance.
更に、熱時におけるインク層との接着力を減じるために
剥離剤として作用する物質を適宜混合して用いてもよい
。Furthermore, in order to reduce the adhesive force with the ink layer when heated, a substance that acts as a release agent may be appropriately mixed and used.
次に本発明の−fンク層に用いられる熱可塑性樹脂につ
いて説明する。熱可塑性樹脂としてはポリアミド系樹脂
、ポリエステル系樹脂、ポリウレタン系樹脂、ポリオレ
フィン樹脂、アクリル系樹脂、塩化ビニル系樹脂、セル
ロース系樹脂、ロジン系(ヨ脂、石油系t、B脂、アイ
オノマー樹脂、天然ゴム、スチレンブタジェンゴム、イ
ンプレンゴム、クロロプレンゴムIJどのエラストマー
nなどを挙ケルことができる。Next, the thermoplastic resin used in the -f layer of the present invention will be explained. Thermoplastic resins include polyamide resins, polyester resins, polyurethane resins, polyolefin resins, acrylic resins, vinyl chloride resins, cellulose resins, rosin resins (oil oil, petroleum-based T, B fat, ionomer resins, natural Examples include elastomers such as rubber, styrene-butadiene rubber, imprene rubber, and chloroprene rubber IJ.
熱可塑性樹脂の水性エマルジョンは、熱溶融性物質の水
性エマルジョンを生成させるのと全く同様の方法を用い
ることができるし、通常のエマルジョン重合法によって
得ることもできる。また、かなり広範囲な水性エマルジ
ョンが市販品として入手できる。以下に具体例2挙げる
。The aqueous emulsion of the thermoplastic resin can be obtained using exactly the same method as for producing an aqueous emulsion of a thermofusible material, or by a conventional emulsion polymerization method. Also, a fairly wide range of aqueous emulsions are commercially available. A second specific example is given below.
0 ポリゾールAP−691(2−二手ルヘキシルアク
リレート系)昭和高分子
0 ニフボールLX−811(アクリル酸エステル系)
日本ゼオン
OモビニールI)M−60(スチレン−アクリル酸基)
ヘキスト化学
ロ JSR−2108(ス千しンーフ゛クジエン系)日
本合成ゴム
0 パイロナールMD−1200(ポリエステル系)東
洋紡
0 ケミバールS −100(アイオノマー系)三井石
油化学
oAD−37F1(ポリエチレン系)東洋インキ0 ザ
イク七ン人(二手しンーアクリル酸系)製鉄化学
0 パンフレックスC1−5000(工千しンー酢酸ビ
ニル系)クラレ
Q ハリニスターDS−90E (oジン系t31脂
)ff?i磨化成
本発明のインク居に用いる着色剤は蕪機顔料、有機顔料
または有機染料の任意のものでよい。無機顔料の例とし
ては、二酸化チタン、カーボンブラック、ffi化亜鉛
、プルシアンブルー、硫化カドミウム、酸化鉄ならびに
鉛、亜鉛、バリウム及びカルシウムのクロム酸塩などが
ある。有機顔料としては、アゾ、千オインジゴ、アント
ラキノン。0 Polysol AP-691 (2-handle hexyl acrylate type) Showa Kobunshi 0 Nifbol LX-811 (acrylic ester type)
Nippon Zeon Omonylin I) M-60 (styrene-acrylic acid group)
Hoechst Chemical Co., Ltd. JSR-2108 (Screen-fixed diene type) Japan Synthetic Rubber 0 Pyronal MD-1200 (Polyester type) Toyobo 0 Chemivar S-100 (Ionomer type) Mitsui Petrochemical oAD-37F1 (Polyethylene type) Toyo Ink 0 Zaik 7 Ninjin (acrylic acid based) Steel Chemical 0 Panflex C1-5000 (vinyl acetate based) Kuraray Q Hallinister DS-90E (Ogin based T31 fat) ff? The coloring agent used in the ink composition of the present invention may be any of pigments, organic pigments, and organic dyes. Examples of inorganic pigments include titanium dioxide, carbon black, zinc ffi, Prussian blue, cadmium sulphide, iron oxides and chromates of lead, zinc, barium and calcium. Organic pigments include azo, thousand oindigo, and anthraquinone.
アントアンスロン、トリフエンジオキサジン系の顔料、
バット染料顔料、フタロシアニン顔料、例えば銅7タロ
シアニン及びその誘導体ならびにキナクリドン顔料など
がある。Anthurone, triphenedioxazine pigments,
These include vat dye pigments, phthalocyanine pigments such as copper-7 thalocyanine and its derivatives, and quinacridone pigments.
有機染料としては、酸性染料、直接染料、分散染料、油
溶性染料、含金属油溶性染料などが拳げられる。Examples of organic dyes include acid dyes, direct dyes, disperse dyes, oil-soluble dyes, and metal-containing oil-soluble dyes.
本発明においてインク層を形成する成分の組成比は限定
されないが、インク層の固形分総量100重n部に対し
、着色剤は5〜40重量部(より好ましくは5〜35重
量部)、熱可塑性樹脂は5〜95重n部(より好ましく
は頷〜90重量部)の使用が好ましい。In the present invention, the composition ratio of the components forming the ink layer is not limited, but the colorant is 5 to 40 parts by weight (more preferably 5 to 35 parts by weight), It is preferable to use the plastic resin in an amount of 5 to 95 parts by weight (more preferably 1 to 90 parts by weight).
本発明のインク層には上記成分の他、各種の添加剤が含
有せしめられてもよい。例えば水性エマルジ叢ンの粘度
を調整するポリアクリル酸ナトリウムの如き増粘剤、ま
たフロイダルシリ力の如キ表面辷り性を向上させる物質
が使用されてもよい。In addition to the above components, the ink layer of the present invention may contain various additives. For example, thickeners such as sodium polyacrylate to adjust the viscosity of the aqueous emulsion, and substances to improve surface slippage such as floidal silicide may be used.
また、アニオン性、カチオン性、/ニオン性、両性界面
活性剤も好適に使用される。Anionic, cationic, /ionic, and amphoteric surfactants are also preferably used.
本発明の感熱転写記録媒体に用いられる支持体は、耐熱
強度を有し、寸法安定性および表面平滑性の高い支持体
が望ましい。材料としては、例えば普通紙、コンデンサ
ー紙、ラミネート紙、コート紙等の紙類、あるいはポリ
エチレン、ポリエチレンテレフタレート、サリスチレン
、ポリプロピレン、ポリイミド等の樹脂フィルムも1お
よび紙−樹脂フィルム複合体、アルミ箔等の金属シート
等がいずれも好適に使用される。支持体の厚さは良好な
熱伝導性をうる上で通常約60μm以下、特に1.5〜
15μmであるのが好ましい。なおまた、本発明の感熱
転写記録媒体は、その支持体裏面側の構成は任意であり
、スティンキング防止層等のパッキンゲ層を設けてもよ
い。The support used in the thermal transfer recording medium of the present invention preferably has heat-resistant strength, high dimensional stability, and high surface smoothness. Examples of materials include papers such as plain paper, condenser paper, laminated paper, and coated paper; resin films such as polyethylene, polyethylene terephthalate, salistyrene, polypropylene, and polyimide; and paper-resin film composites, aluminum foil, etc. Metal sheets and the like are preferably used. The thickness of the support is usually about 60 μm or less, particularly 1.5 to 1.5 μm, in order to obtain good thermal conductivity.
Preferably, it is 15 μm. Furthermore, in the thermal transfer recording medium of the present invention, the structure on the back side of the support may be optional, and a packing layer such as a stinking prevention layer may be provided.
本発明の感熱転写記録媒体を用いて熱転写記録する方法
について以下に述べる。A method for thermal transfer recording using the thermal transfer recording medium of the present invention will be described below.
本発明の感熱転写記録媒体の構成層面と普通紙の如き記
録シートとを重ねて、画像の情報に応じてサーマルヘッ
ドやサーマルペン或いはレーザーを用いる熱記録装置に
よって感熱転写記録媒体側から及び/又は記録シート側
からエネルギーを与えると、インク層は比較的低いエネ
ルギーを与えられることによって記録紙と接着し、感熱
転写記録媒体が記録紙と実質的に離れる際インク層が記
録紙に転写される。The component layer surface of the thermal transfer recording medium of the present invention and a recording sheet such as plain paper are overlapped, and depending on the image information, a thermal recording device using a thermal head, a thermal pen, or a laser is used to print from the thermal transfer recording medium side and/or When energy is applied from the recording sheet side, the ink layer adheres to the recording paper due to the application of relatively low energy, and when the thermal transfer recording medium is substantially separated from the recording paper, the ink layer is transferred to the recording paper.
本発明の感熱転写記録媒体を用いることによって、以下
のような効果が得られる。By using the thermal transfer recording medium of the present invention, the following effects can be obtained.
(1) 表面平滑度の低いラフペーパーにも高濃度で
鮮明な印字ができる。(1) High density and clear printing is possible even on rough paper with low surface smoothness.
(2) 印字に際してのカスレ、滲み、地汚れがない
。(2) There is no fading, bleeding, or scumming during printing.
(3) 感熱転写記録媒体のプロッキンゲ耐性が向上
する。(3) The blocking resistance of the thermal transfer recording medium is improved.
以下、本発明の実施例を挙げるが、本発明がこれにより
限定されることはない。なお、以下に用いる「部」とは
「重量部」を示す。Examples of the present invention will be described below, but the present invention is not limited thereto. Note that "parts" used below indicate "parts by weight."
3.5 tIm のポリエチレンテレフタレートフィ
ルム上に下記の塗布組成物をワイヤーバーを用いて乾燥
膜厚 3.0μmになるよう塗布し、本発明のTmを形
成した。The following coating composition was coated onto a polyethylene terephthalate film of 3.5 tIm using a wire bar so as to have a dry film thickness of 3.0 μm to form the Tm of the present invention.
パラフィンワックスエマルジヲン(a 点70℃のパラ
フィンワックスをボリエチレンゲリフールモノステアリ
ルエーテルで水に乳化したエマルシヨン 固型分30%
)・・・・・・・・・・・・・・・・・・・・・・・・
・・ 85、Z二手しンー酢酸ビニル共重合体エマルジ
ョン(アドフー) AD−37P295 東洋モー
トン社製 固型分・10%)・・・・・・・・・・・・
・・・・・・・・・・・・・・11.25部弗素系界面
活性剤(FT−248バイエル社製)2%水溶液・・・
・・・・・・・・・・・・・・・・・・・・・・・・・
・・・・・・・・・・・・・・・・・・・・2.5部次
に表1に示す如きインク組成物をTmの上に乾燥膜1ワ
1.2pm になるよう塗布し、本発明の、感熱転写
記録媒体試料8種(1−Vl)を得た。Paraffin wax emulsion (a emulsion made by emulsifying paraffin wax at a temperature of 70°C in water with polyethylene gelyfur monostearyl ether, solid content 30%)
)・・・・・・・・・・・・・・・・・・・・・
85, Z two-handed shin-vinyl acetate copolymer emulsion (Adfu) AD-37P295 Manufactured by Toyo Morton Co., Ltd. Solid content: 10%)
・・・・・・・・・・・・・・・11.25 parts fluorine surfactant (FT-248 manufactured by Bayer AG) 2% aqueous solution...
・・・・・・・・・・・・・・・・・・・・・・・・
・・・・・・・・・・・・・・・・・・・・・2.5 parts Next, apply an ink composition as shown in Table 1 on Tm so that the dry film thickness is 1.2 pm. Eight kinds of thermal transfer recording medium samples (1-Vl) of the present invention were obtained.
以下余白
感熱転写記録媒体試料をサーマルプリンター(2,1d
at シリアルヘッド、印字圧600g/ヘッド。The following margin thermal transfer recording medium sample was printed on a thermal printer (2,1d
at serial head, printing pressure 600g/head.
プラテンゴム硬度50’の試作機)を用いて普通紙とラ
フペーパーに記D(印字)した。なお、普通紙は市販の
フビー用紙(ペック平滑度(9)秒)を、ラフペーパー
はポンド紙(同10秒)を用いた。いずれの紙に対して
もカスレ、滲み、地汚れのない・鮮明な印字が得られた
。また、これらの感熱転写記録媒体は長期保存してもブ
ロッキングを生じなかった。D (printing) was performed on plain paper and rough paper using a prototype machine with a platen rubber hardness of 50'. Note that commercially available flat paper (Peck smoothness: 9 seconds) was used as the plain paper, and pound paper (Peck smoothness: 10 seconds) was used as the rough paper. Clear prints with no fading, bleeding, or scumming were obtained on all papers. Furthermore, these thermal transfer recording media did not cause blocking even after long-term storage.
比(り例 l
実施例におけるインク層を 3.0 Amで塗布して得
た感熱転写記録媒体試料を用いて、実施例と同様に印字
したところ、全ての試料が殆んど印字さt’L rjか
ったり、著しい印字モレを生じた。Ratio (Example 1) When printing was performed in the same manner as in the example using heat-sensitive transfer recording medium samples obtained by applying the ink layer in the example at 3.0 Am, all the samples showed almost no printing. L rj was distorted and significant printing leakage occurred.
比(り例 2
実施例において、水の代りにメチルエチルケトン/トル
エン混合溶媒に溶解、分散させたインク組成物を実施例
と同様1.2 am に撒布して得た感熱転写記録媒
体試料を用いて、実施例と同様に印字したところ、印字
のエツジ部分に著しいヒゲを発生した。また、これらの
感熱転写記録媒体は保存により著しいブロッキングを生
じた。Ratio (Example 2) In Example 2, a thermal transfer recording medium sample obtained by dispersing an ink composition dissolved and dispersed in a mixed solvent of methyl ethyl ketone/toluene instead of water at 1.2 am as in Example was used. When printing was carried out in the same manner as in Examples, significant whiskers occurred at the edge portions of the prints.Also, these thermal transfer recording media exhibited significant blocking during storage.
比較例 3
実施例における下層の塗布組成物において、水の代りに
トルエンを用いて加温、塗布して形成した壬下層の上に
、表1のインク組成物を塗布したところ、著しいハジキ
現象が生じ満足な感熱転写記録媒体は得られなかった。Comparative Example 3 When the ink composition shown in Table 1 was applied on the lower layer formed by heating and applying toluene instead of water in the lower layer coating composition in the example, a remarkable repelling phenomenon was observed. Therefore, a satisfactory thermal transfer recording medium could not be obtained.
Claims (2)
ジョンを含有する層と、その上に熱可塑性樹脂の水性エ
マルジョンを含有するインク層を少なくとも一層有する
感熱転写記録媒体であって、前記インク層の膜厚が2μ
m以下であることを特徴とする感熱転写記録媒体。(1) A thermal transfer recording medium having, on a support, at least a layer containing an aqueous emulsion of a thermofusible substance, and at least one ink layer containing an aqueous emulsion of a thermoplastic resin thereon, the ink layer The film thickness is 2μ
A heat-sensitive transfer recording medium characterized in that it has a diameter of less than m.
層の膜厚が、前記インク層の膜厚より厚いことを特徴と
する特許請求の範囲第1項記載の感熱転写記録媒体。(2) The heat-sensitive transfer recording medium according to claim 1, wherein the layer containing the aqueous emulsion of the heat-melting substance is thicker than the ink layer.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60224046A JPH0714663B2 (en) | 1985-10-07 | 1985-10-07 | Thermal transfer recording medium |
| US06/913,323 US4818591A (en) | 1985-10-07 | 1986-09-30 | Thermal transfer recording medium |
| DE19863634049 DE3634049A1 (en) | 1985-10-07 | 1986-10-07 | HEAT TRANSFER RECORDING MEDIUM |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60224046A JPH0714663B2 (en) | 1985-10-07 | 1985-10-07 | Thermal transfer recording medium |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6282085A true JPS6282085A (en) | 1987-04-15 |
| JPH0714663B2 JPH0714663B2 (en) | 1995-02-22 |
Family
ID=16807745
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60224046A Expired - Lifetime JPH0714663B2 (en) | 1985-10-07 | 1985-10-07 | Thermal transfer recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0714663B2 (en) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6061290A (en) * | 1983-09-14 | 1985-04-09 | Pilot Pen Co Ltd:The | Thermal transfer recording medium |
| JPS60187593A (en) * | 1984-03-06 | 1985-09-25 | Canon Inc | Thermal transfer material |
-
1985
- 1985-10-07 JP JP60224046A patent/JPH0714663B2/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6061290A (en) * | 1983-09-14 | 1985-04-09 | Pilot Pen Co Ltd:The | Thermal transfer recording medium |
| JPS60187593A (en) * | 1984-03-06 | 1985-09-25 | Canon Inc | Thermal transfer material |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0714663B2 (en) | 1995-02-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4818591A (en) | Thermal transfer recording medium | |
| JPH0548756B2 (en) | ||
| JP2579145B2 (en) | Thermal transfer recording medium | |
| EP0194860B1 (en) | Heat-sensitive transferring recording medium | |
| JPS633994A (en) | Thermal transfer recording medium | |
| JPS60234888A (en) | Thermal transfer recording medium | |
| JPS6282085A (en) | Thermal transfer recording medium | |
| JPH0357696A (en) | Thermal transfer recording medium | |
| JPS6382784A (en) | Transfer type thermal recording medium | |
| JP2926766B2 (en) | Thermal transfer recording medium | |
| JPH01171886A (en) | Thermal transfer recording medium | |
| JPH06312567A (en) | Thermal transfer recording medium | |
| JPS63183882A (en) | Thermal transfer recording medium | |
| JP2686610B2 (en) | Manufacturing method of thermal transfer sheet | |
| JPH0461798B2 (en) | ||
| JPS62231789A (en) | Production of thermal transfer recording medium | |
| JPS633995A (en) | Thermal transfer recording medium | |
| JPS60234890A (en) | Thermal transfer recording medium | |
| JP3299795B2 (en) | Thermal transfer sheet | |
| JPH01190491A (en) | Thermal transfer recording medium | |
| JPH042438B2 (en) | ||
| JPH11268426A (en) | Thermal transfer recording medium, method for manufacturing the same, and thermal transfer recording method | |
| JPH04156386A (en) | Thermally transferable recording medium | |
| JPH01171885A (en) | Thermal transfer recording medium | |
| JP2989836B2 (en) | Thermal transfer recording medium |