JP2620266B2 - Thermal transfer media - Google Patents
Thermal transfer mediaInfo
- Publication number
- JP2620266B2 JP2620266B2 JP62300576A JP30057687A JP2620266B2 JP 2620266 B2 JP2620266 B2 JP 2620266B2 JP 62300576 A JP62300576 A JP 62300576A JP 30057687 A JP30057687 A JP 30057687A JP 2620266 B2 JP2620266 B2 JP 2620266B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- layer
- adhesive layer
- resin
- thermal transfer
- 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.)
- Expired - Lifetime
Links
- 229920005989 resin Polymers 0.000 claims description 53
- 239000011347 resin Substances 0.000 claims description 53
- 239000010410 layer Substances 0.000 claims description 31
- 239000012790 adhesive layer Substances 0.000 claims description 29
- 230000001681 protective effect Effects 0.000 claims description 18
- 229920000642 polymer Polymers 0.000 claims description 10
- 238000001465 metallisation Methods 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000011247 coating layer Substances 0.000 claims description 5
- 239000006185 dispersion Substances 0.000 claims description 4
- 238000003475 lamination Methods 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 51
- 238000000576 coating method Methods 0.000 description 21
- 239000011248 coating agent Substances 0.000 description 18
- 239000000243 solution Substances 0.000 description 17
- 239000001993 wax Substances 0.000 description 15
- 239000000123 paper Substances 0.000 description 13
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 12
- 239000012046 mixed solvent Substances 0.000 description 11
- 229910052782 aluminium Inorganic materials 0.000 description 10
- -1 polyethylene Polymers 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- 239000010408 film Substances 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 6
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 239000002932 luster Substances 0.000 description 6
- 239000012188 paraffin wax Substances 0.000 description 6
- 229920006267 polyester film Polymers 0.000 description 6
- 229920000178 Acrylic resin Polymers 0.000 description 5
- 239000004925 Acrylic resin Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 239000001293 FEMA 3089 Substances 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 229920003048 styrene butadiene rubber Polymers 0.000 description 4
- 239000010409 thin film Substances 0.000 description 4
- DTCCVIYSGXONHU-CJHDCQNGSA-N (z)-2-(2-phenylethenyl)but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)\C=CC1=CC=CC=C1 DTCCVIYSGXONHU-CJHDCQNGSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000004203 carnauba wax Substances 0.000 description 3
- 235000013869 carnauba wax Nutrition 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 238000001771 vacuum deposition Methods 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 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
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 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
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 229910034327 TiC Inorganic materials 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229940092738 beeswax Drugs 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000012170 montan wax Substances 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
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002647 polyamide 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
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 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
- B41M5/38207—Contact thermal transfer or sublimation processes characterised by aspects not provided for in groups B41M5/385 - B41M5/395
- B41M5/38214—Structural details, e.g. multilayer systems
-
- 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
-
- 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
- B41M5/40—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
- B41M5/426—Intermediate, backcoat, or covering layers characterised by inorganic compounds, e.g. metals, metal salts, metal complexes
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Description
【発明の詳細な説明】 [技術分野] 本発明は、プリンタ、ファクシミリ等の感熱転写装置
に用いられる感熱転写媒体に関し、更に詳しくは、金銀
等の金属光沢の文字画像を平滑度の低い被記録紙に記録
できる様にしたラフ紙対応の感熱転写媒体に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thermal transfer medium used for a thermal transfer device such as a printer or a facsimile, and more specifically, to record a character image of metallic luster such as gold and silver with low smoothness. The present invention relates to a thermal transfer medium for rough paper which can be recorded on paper.
[従来の技術] 従来より、一般に感熱転写媒体用接着剤としては、ワ
ックス系分散型接着剤と溶剤型高分子接着剤の単独また
は混合系が用いられていた。[Prior Art] Conventionally, as an adhesive for a thermal transfer medium, a wax-based dispersion-type adhesive and a solvent-type polymer adhesive have been used alone or in combination.
しかし、本発明の如き高い金属光沢性を有する感熱転
写媒体において上記接着剤を単独または混合系において
使用した場合、各々長所と共に次のような欠点が認めら
れ広範囲なラフ紙への対応が難しかった。However, when the above-mentioned adhesives are used alone or in a mixed system in the heat-sensitive transfer medium having a high metallic gloss as in the present invention, the following disadvantages are recognized together with the advantages, and it is difficult to cope with a wide range of rough paper. .
ワックス系分散型接着剤単独の場合 熱伝導性が良すぎるため溶融粘度が低く、印字の際の
欠け現象(一般に中抜け、逆転写等と呼ばれている現
象)が起こり易く、ベック平滑度100sec.以下、とりわ
け50sec.以下のラフ紙への印字が困難である。When the wax-based dispersion-type adhesive alone is used, its thermal conductivity is too good, so that its melt viscosity is low, and chipping phenomena during printing (general phenomena generally called voids, reverse transfer, etc.) tend to occur, and Beck smoothness is 100 sec. It is difficult to print on rough paper of less than 50 sec.
溶剤可溶型高分子接着剤単独の場合 熱伝導性が悪く高速印字に対応できない。When the solvent-soluble polymer adhesive alone is used, the thermal conductivity is poor and high-speed printing cannot be performed.
分子量が大きいため、印字の切れ性(シャープさ)が
悪い。Poor print sharpness (sharpness) due to high molecular weight.
混合系の場合 前記二者の欠点がでる。即ち、熱伝導性が良すぎるた
め溶融粘度が低く、印字の際の欠け現象(一般に中抜
け、逆転写等と呼ばれている現象)が起こり易く、ベッ
ク平滑度100sec.以下、とりわけ50sec.以下のラフ紙へ
の印字が困難である。In the case of a mixed system, the above two drawbacks appear. That is, since the thermal conductivity is too good, the melt viscosity is low, and a chipping phenomenon at printing (generally a phenomenon called hollow, reverse transfer, etc.) is likely to occur, and a Beck smoothness of 100 sec. Or less, especially 50 sec. Or less. Is difficult to print on rough paper.
熱伝導性が悪く高速印字に対応できない。 Poor thermal conductivity makes high speed printing impossible.
分子量が大きいため、印字の切れ性(シャープさ)が
悪い。Poor print sharpness (sharpness) due to high molecular weight.
[発明の目的] 本発明は上記従来の欠点に鑑み、極めて良好な金属光
沢を有した転写像等の記録ができる感熱転写媒体を提供
することにある。[Object of the Invention] The present invention has been made in view of the above-mentioned conventional drawbacks, and has as its object to provide a heat-sensitive transfer medium capable of recording a transfer image or the like having extremely good metallic luster.
[発明の構成] ベースフイルムの上に直接または離型剤層を介して、
少なくとも保護樹脂塗膜層、金属蒸着層、接着剤層を順
次形成した感熱転写媒体において、接着剤層がワックス
系分散型接着剤層と溶剤可溶型高分子接着剤層をこの順
に積層されてなることを特徴とするラフ紙対応型感熱転
写媒体に関するものである。[Constitution of the Invention] Directly on a base film or via a release agent layer,
In a thermal transfer medium in which at least a protective resin coating layer, a metal deposition layer, and an adhesive layer are sequentially formed, the adhesive layer is formed by laminating a wax-based dispersed adhesive layer and a solvent-soluble polymer adhesive layer in this order. The present invention relates to a thermal transfer medium for rough paper.
即ち本発明の感熱転写媒体においては、従来感熱転写
媒体の単層の接着剤層にかえてワックス系分散型接着剤
層と溶剤可溶型高分子接着剤層をこの順に積層した複合
層を用いることによって、熱伝導性が良くなり、シャー
プな印字が得られる。更に印字の際の欠け現象が起こり
にくくなり、ベック平滑度100sec.以下とりわけ50sec.
以下のラフ紙への印字が可能な極めて良好な金属光沢を
有した転写像等の記録ができる感熱転写媒体を完成した
ものである。That is, in the thermal transfer medium of the present invention, a composite layer in which a wax-based dispersion type adhesive layer and a solvent-soluble type polymer adhesive layer are laminated in this order instead of a single adhesive layer of a conventional thermal transfer medium is used. As a result, thermal conductivity is improved, and sharp printing is obtained. Furthermore, the chipping phenomenon during printing is less likely to occur, and the Bekk smoothness is 100 sec. Or less, especially 50 sec.
The present invention has completed a heat-sensitive transfer medium capable of recording a transfer image or the like having extremely good metallic luster that can be printed on rough paper.
即ち本発明は、ベースフイルム(1)の上に直接また
は離型剤層(2)を介して、少なくとも保護樹脂塗膜層
(3)、金属蒸着層(4)、接着剤層(5)を順次形成
した感熱転写媒体において、接着剤層(5)がワックス
系分散型接着剤層(51)と溶剤可溶型高分子接着剤層
(52)をこの順に積層形成したことにより極めて良好な
金属光沢を有した転写像等の記録ができる感熱転写媒体
を提供することを可能としたものである。That is, according to the present invention, at least the protective resin coating layer (3), the metal deposition layer (4), and the adhesive layer (5) are provided directly on the base film (1) or via the release agent layer (2). In the thermal transfer medium formed sequentially, the adhesive layer (5) was formed by laminating a wax-based dispersion type adhesive layer (51) and a solvent-soluble type polymer adhesive layer (52) in this order, resulting in extremely good metal. An object of the present invention is to provide a thermal transfer medium capable of recording a glossy transfer image or the like.
本発明の感熱転写媒体におけるベースフイルム(1)
としては充分な自己保持性を有するものであればいずれ
も用いられるが、たとえばポリエステル、ポリアミドポ
リアドイミド、ポリエチレン、ポリプロピレン、セルロ
ースアセテート、ポリカーボネート、ポリ塩化ビニル、
フッ素樹脂などの樹脂類またはセロハン紙、グラシン紙
などのフイルム状物またはシート状物や剥離紙または楽
離フイルムなどが適宜用いられる。特にベースフイルム
(1)としては前記樹脂類のフイルム状物で厚さが2.5
〜12μm程度のものを用いるのが、しわや亀裂などのな
い感熱転写媒体の製造が連続的に大量生産できる点から
好ましい。また先に本出願人が出願した発明(特願昭60
−260774号)に記載されている様な、プラスチックフイ
ルムの熱転写層を設ける側の反対泡に無機物の薄膜、例
えばSiO、SiO2、TiO2、ZnO、Al2O3等の酸化物、TiN等の
チッ化物、TiC等の炭化物、炭素、Al、Ni、Cr、Ti、Ni
−Cr合金等の金属の6〜100nm程度の薄膜を設けた耐ホ
ットスティク性加工したものも好ましく用いられる。Base film in thermal transfer medium of the present invention (1)
Any one can be used as long as it has a sufficient self-holding property, for example, polyester, polyamide polyadimide, polyethylene, polypropylene, cellulose acetate, polycarbonate, polyvinyl chloride,
Resins such as fluororesin, or film-like or sheet-like materials such as cellophane paper and glassine paper, release paper or release film are used as appropriate. In particular, the base film (1) is a film-like material of the above-mentioned resins and has a thickness of 2.5
It is preferable to use one having a thickness of about 12 μm because a thermal transfer medium free of wrinkles and cracks can be continuously mass-produced. In addition, the invention (Japanese Patent Application No.
-260774), a thin film of an inorganic substance, for example, an oxide such as SiO, SiO 2 , TiO 2 , ZnO, Al 2 O 3 , TiN, etc., in the bubble opposite to the side on which the thermal transfer layer of the plastic film is provided. Nitride, carbide such as TiC, carbon, Al, Ni, Cr, Ti, Ni
A hot-stick resistant material provided with a thin film of about 6 to 100 nm of a metal such as a -Cr alloy is also preferably used.
尚、ベースフイルム(1)が保護樹脂塗膜層(3)と
の剥離性がよくない場合にはパラフィンワックス、シリ
コーン、フッ素樹脂、界面活性剤などを塗布して離型剤
層(2)を形成しておいてもよい。When the base film (1) does not have good releasability from the protective resin coating layer (3), a paraffin wax, silicone, a fluororesin, a surfactant or the like is applied to form the release agent layer (2). It may be formed.
本発明の感熱転写媒体において、金属蒸着層事態は機
械的強度が弱く摩擦による損傷などを受けやすいので、
金属蒸着層の面上に保護樹脂塗膜を設ける。保護樹脂塗
膜の厚さは特に制限は無いが通常0.5〜2μmの範囲か
ら適宜選ばれる。In the thermal transfer medium of the present invention, the metal deposited layer is easily damaged by friction due to low mechanical strength,
A protective resin coating is provided on the surface of the metal deposition layer. The thickness of the protective resin coating is not particularly limited, but is usually appropriately selected from the range of 0.5 to 2 μm.
かかる保護樹脂塗膜を形成するための樹脂としては、
たとえば熱可塑性樹脂、熱硬化性樹脂、電子線硬化樹
脂、紫外線硬化性樹脂のいずれもが用いられ、たとえば
アクリル系樹脂、塩化ビニル−酢酸ビニル共重合体、ポ
リビニルブチラール、ポリカーボネート、ニトロセルロ
ース、セルロースアテテート、ウレタン系樹脂、尿素系
樹脂、メラミン系樹脂、尿素−メラミン系樹脂、エポキ
シ系樹脂、アルキッド系樹脂、アミノアルキッド系樹
脂、ロジン変性マレイン酸樹脂などの単独または混合物
が好ましく用いられる。As a resin for forming such a protective resin coating film,
For example, any of a thermoplastic resin, a thermosetting resin, an electron beam curable resin, and an ultraviolet curable resin may be used. For example, acrylic resin, vinyl chloride-vinyl acetate copolymer, polyvinyl butyral, polycarbonate, nitrocellulose, cellulose acetate Tate, urethane-based resins, urea-based resins, melamine-based resins, urea-melamine-based resins, epoxy-based resins, alkyd-based resins, aminoalkyd-based resins, rosin-modified maleic acid resins, and the like, or a mixture thereof are preferably used.
保護樹脂層の形成は、前記保護樹脂塗膜を形成するた
めの樹脂の有機溶剤溶液、水溶液などをロールコーティ
ング法、グラビアコーティング法、リバースコーティン
グ法、スプレイコーティング法などの通常のコーティン
グ法により塗布し、乾燥(熱硬化性樹脂、電子線硬化性
樹脂、紫外線硬化性樹脂などの場合は硬化)することに
よって行われる。The protective resin layer is formed by applying an organic solvent solution of the resin for forming the protective resin coating film, an aqueous solution, or the like by a normal coating method such as a roll coating method, a gravure coating method, a reverse coating method, and a spray coating method. And drying (in the case of a thermosetting resin, an electron beam curable resin, an ultraviolet curable resin, etc., curing).
保護樹脂層はそれが透明または半透明である限りにお
いて染料または顔料などの着色材で着色してもよい。The protective resin layer may be colored with a coloring material such as a dye or a pigment as long as it is transparent or translucent.
本発明の感熱転写媒体の金属蒸着層(4)は前記保護
樹脂層の上に常法によりたとえアルミニウム、銅、銀、
金などの金属またはそれらの合金を蒸着して形成される
が、光沢性とコストの点からアルミニウムが最も好まし
い。The metal-deposited layer (4) of the thermal transfer medium of the present invention is formed on the protective resin layer by a conventional method such as aluminum, copper, silver, or the like.
It is formed by depositing a metal such as gold or an alloy thereof, and aluminum is most preferable in terms of gloss and cost.
前記金属蒸着層としては、公知の真空蒸着法、スパッ
タリング法、イオンプレイティング法などの通常の金属
(合金も含む、以下同様)の薄膜形成方法により、たと
えば亜鉛、アルミニウム、ガリウム、インジウム、錫、
ニッケル、銀、金、銅、珪素、クロム、チタン、白金、
パラジウムなどの蒸着が可能な単体または混合物あるい
は合金等が厚さ10〜100nm程度に蒸着形成される。厚さ
が10nm程度以下の場合には金属光沢が殆ど認められず金
属蒸着層を設けた価値が無く、また100nm程度以上に形
成しても金属光沢に変化がなく経済的でない。尚、金属
蒸着層は一層とせず、複数層としても良く、その場合に
は層毎に金属の種類をかえてもよい。また表面側に位置
する金属蒸着層の厚さを30nm程度以下として内側に位置
する金属蒸着との間に透明樹脂や透明無機金属化合物か
らなる干渉薄膜層を介在させて干渉虹彩色を発生させる
ようにしてもよい。As the metal deposited layer, for example, zinc, aluminum, gallium, indium, tin, and the like may be formed by a known metal (including alloy, hereinafter the same) thin film forming method such as a known vacuum deposition method, a sputtering method, and an ion plating method.
Nickel, silver, gold, copper, silicon, chromium, titanium, platinum,
A single substance, a mixture, an alloy, or the like capable of being deposited such as palladium is deposited to a thickness of about 10 to 100 nm. When the thickness is about 10 nm or less, almost no metallic luster is recognized, and there is no value in providing a metal vapor-deposited layer. Even when the thickness is about 100 nm or more, the metallic luster does not change and is not economical. The metal deposition layer is not limited to one layer but may be a plurality of layers. In this case, the type of metal may be changed for each layer. Also, the thickness of the metal deposition layer located on the surface side is set to about 30 nm or less so that an interference thin film layer made of a transparent resin or a transparent inorganic metal compound is interposed between the metal deposition located on the inner side to generate an interference iris color. It may be.
本発明の感熱転写媒体のワックス系分散型接着剤層
(51)としてはたとえば鯨ロウ、ミツロウ、ラノリン、
カルバナワックス、キャンデリラワックス、モンタンワ
ックスなどの天然ワックス、パラフィンワックス、マイ
クロクリンワックス、酸化ワックス、エステルワック
ス、低分子量ポリエチレンなどの合成ワックス類にタッ
キファイヤー充填剤、可塑剤、酸化防止剤などの単独又
は混合されたものが用いられる。ワックス系分散型接着
剤層(51)の厚さは被転写紙の表面状態などにより適宜
選択決定されるものであるが通常は1〜10μm程度の範
囲から選ばれ、通常の被転写紙の表面が比較的平滑な場
合には比較的薄い1〜2μm程度である。Examples of the wax-based dispersed adhesive layer (51) of the thermal transfer medium of the present invention include spermaceti, beeswax, lanolin,
Natural waxes such as carbana wax, candelilla wax, montan wax, synthetic waxes such as paraffin wax, microclean wax, oxidized wax, ester wax, and low molecular weight polyethylene, as well as tackifier fillers, plasticizers, antioxidants, etc. A single material or a mixture thereof is used. The thickness of the wax-based dispersed adhesive layer (51) is appropriately selected and determined according to the surface condition of the paper to be transferred, but is usually selected from a range of about 1 to 10 μm. Is relatively thin, about 1-2 μm.
本発明の感熱転写媒体の溶剤可溶型高分子接着剤層
(52)としてはたとえばラウリン酸、ミリスチン酸、パ
ルミチン酸、ステアリン酸、フロメン酸、ベヘニン酸な
どの高級脂肪酸、ステアリルアルコール、ベヘニルアル
コールなどの高級アルコール、ショ糖の脂肪酸エステ
ル、ソルビタンの脂肪酸エステルなどのエステル類、ス
テアリンアミド、オレインアミドなどのアミド類、ポリ
アミド系樹脂、ポリエステル系樹脂、エポキシ系樹脂、
ポリウレタン系樹脂、アクリル系樹脂、塩化ビニル系樹
脂、セルロース系樹脂、ポリビニール系樹脂、石油系樹
脂、エチレン−酢酸ビニル共重合体樹脂、フエノール系
樹脂、スチレン系樹脂、天然ゴム、スチレンブタジエン
ゴム、イソプレンゴム、クロロプレンゴムなどのエラス
トマー類、ロジンおよびその誘導体、テルペン樹脂、水
添石油樹脂類にタッキファイヤー充填剤、可塑剤、酸化
防止剤などの単独または混合されたものが用いられる。
溶剤可溶型高分子接着剤層(52)の厚さは被転写紙の表
面状態などにより適宜選択決定されるものであるが通常
は1〜10μm程度の範囲から選ばれ、通常の被転写紙の
表面が比較的平滑な場合には比較的薄い1〜2μm程度
である。Examples of the solvent-soluble polymer adhesive layer (52) of the thermal transfer medium of the present invention include higher fatty acids such as lauric acid, myristic acid, palmitic acid, stearic acid, phlomenic acid and behenic acid, stearyl alcohol and behenyl alcohol. Esters such as higher alcohols, fatty acid esters of sucrose, fatty acid esters of sorbitan, amides such as stearinamide and oleinamide, polyamide resins, polyester resins, epoxy resins,
Polyurethane resin, acrylic resin, vinyl chloride resin, cellulose resin, polyvinyl resin, petroleum resin, ethylene-vinyl acetate copolymer resin, phenol resin, styrene resin, natural rubber, styrene butadiene rubber, Elastomers such as isoprene rubber and chloroprene rubber, rosin and derivatives thereof, terpene resins, hydrogenated petroleum resins, and the like, alone or mixed with a tackifier filler, a plasticizer, an antioxidant, and the like are used.
The thickness of the solvent-soluble polymer adhesive layer (52) is appropriately selected and determined according to the surface condition of the paper to be transferred, but is usually selected from the range of about 1 to 10 μm. Is relatively thin, about 1 to 2 μm when the surface is relatively smooth.
つぎに実施例をあげて本発明を説明する。 Next, the present invention will be described with reference to examples.
[実施例] 実施例1 厚さ3.5μmのポリエステルフイルム上にアクリル樹
脂20部(重量部、以下同じ)および塩化ゴム10部をトル
エン30部、メチルイソブチルケトン20部およびシクロヘ
キサノン20部からなる混合溶剤に溶解してなるコーティ
ング溶液を塗布、乾燥して厚さ2μmの保護樹脂層を形
成し、その上にアルミニウムを真空蒸着法で40nmの厚さ
に蒸着し、更にその上にカルナバワックス20部をトルエ
ン80部に溶解して成るコーティング溶液を塗布乾燥して
厚さ2μmのワックス系分散型接着剤層を形成し、続い
て更にその上にスチレンブタジエンゴム10部、塩素化ポ
リプロピレン7部、キシレン樹脂15部をトルエン50部、
酢酸エチル50部に溶解してなるコーティング溶液を塗布
乾燥し、厚さ2μmの溶剤可溶型高分子接着剤層を形成
して本発明の感熱転写媒体を得た。[Example] Example 1 A mixed solvent composed of 20 parts of an acrylic resin (parts by weight, the same applies hereinafter) and 10 parts of chlorinated rubber, 30 parts of toluene, 20 parts of methyl isobutyl ketone, and 20 parts of cyclohexanone on a 3.5-μm-thick polyester film. Is applied and dried to form a protective resin layer having a thickness of 2 μm, aluminum is deposited thereon by vacuum evaporation to a thickness of 40 nm, and 20 parts of carnauba wax is further placed thereon. A coating solution formed by dissolving in 80 parts of toluene is applied and dried to form a wax-type dispersed adhesive layer having a thickness of 2 μm. Then, 10 parts of styrene-butadiene rubber, 7 parts of chlorinated polypropylene, and xylene resin are further formed thereon. 15 parts 50 parts toluene,
A coating solution dissolved in 50 parts of ethyl acetate was applied and dried to form a solvent-soluble polymer adhesive layer having a thickness of 2 μm to obtain a thermal transfer medium of the present invention.
実施例2 厚さ6μmのポリエステルフイルム上にパラフィンワ
ックス9部およびケトン樹脂1部をトルエン70部、テレ
ビン油10部および石油ナフサ10部からなる混合溶剤に溶
解して成るコーティング溶液を塗布乾燥して厚さ1μm
の離型剤層を形成し、次いでその面上にスチレンマレイ
ン酸樹脂25部および油性染料55部をトルエン30部、メチ
ルイソブチルケトン20部およびシクロヘキサノン20部か
らなる混合溶剤に溶解してなるコーティング溶液を塗布
乾燥して厚さ2μmの保護樹脂層を形成し、その上にア
ルミニウムを真空蒸着法で厚さ40nmに蒸着し、更にその
上にカルナバワックス20部をトルエン80部に溶解してな
るコーティング溶液を塗布乾燥して厚さ2μmのワック
ス系分散型接着剤層を形成し、続いて更にその上にスチ
レンブタジエンゴム10部、塩素化ポリプロピレン7部、
キシレン樹脂15部をトルエン50部、酢酸エチル50部に溶
解して成るコーティング溶液を塗布乾燥して厚さ2μm
の溶剤可溶型高分子接着剤層を形成して本発明の感熱転
写媒体を得た。Example 2 A coating solution obtained by dissolving 9 parts of paraffin wax and 1 part of ketone resin in a mixed solvent consisting of 70 parts of toluene, 10 parts of turpentine oil and 10 parts of petroleum naphtha was coated on a 6 μm thick polyester film, and dried. 1 μm
A coating solution formed by dissolving 25 parts of a styrene maleic acid resin and 55 parts of an oily dye in a mixed solvent consisting of 30 parts of toluene, 20 parts of methyl isobutyl ketone and 20 parts of cyclohexanone Is applied and dried to form a protective resin layer with a thickness of 2 μm, on which aluminum is vapor-deposited to a thickness of 40 nm by vacuum vapor deposition, and then 20 parts of carnauba wax is dissolved in 80 parts of toluene. The solution was applied and dried to form a wax-based dispersed adhesive layer having a thickness of 2 μm, followed by 10 parts of styrene-butadiene rubber, 7 parts of chlorinated polypropylene,
A coating solution comprising 15 parts of xylene resin dissolved in 50 parts of toluene and 50 parts of ethyl acetate is applied and dried to a thickness of 2 μm.
To form a heat-sensitive transfer medium of the present invention.
比較例1 厚さ35μmのポリエステルフイルム上にアクリル樹脂
20部および塩化ゴム10部をトルエン30部、メチルイソブ
チルケトン20部およびシクロヘキサノン20部からなる混
合溶剤に溶解してなるコーティング溶液を塗布乾燥して
厚さ2μmの保護樹脂層を形成し、その上にアルミニウ
ムを真空蒸着法で40nmの厚さに蒸着し、更にその上にミ
ツロウ20部をトルエン80部に溶解してなるコーティング
溶液を塗布乾燥して厚さ2μmの接着剤層を形成して感
熱転写媒体を得た。Comparative Example 1 Acrylic resin on 35 μm thick polyester film
A coating solution obtained by dissolving 20 parts and 10 parts of chlorinated rubber in a mixed solvent consisting of 30 parts of toluene, 20 parts of methyl isobutyl ketone and 20 parts of cyclohexanone is applied and dried to form a protective resin layer having a thickness of 2 μm. Then, aluminum is deposited to a thickness of 40 nm by a vacuum deposition method, and a coating solution obtained by dissolving 20 parts of beeswax in 80 parts of toluene is applied thereon and dried to form an adhesive layer having a thickness of 2 μm. A thermal transfer medium was obtained.
比較例2 厚さ6μmのポリエステルフイルム上にパラフィンワ
ックス9部およびケトン樹脂1部をトルエン70部、テレ
ピン油10部および石油ナフサ10部からなる混合溶剤に溶
解してなるコーティング溶液を塗布乾燥して厚さ1μm
の離型剤層を形成し、次いでその面上にスチレンマレイ
ン酸樹脂25部および油性染料5部をトルエン30部、メチ
ルイソブチルケトン20部およびシクロヘキサノン20部か
らなる混合溶剤に溶解してなるコーティング溶液を塗布
乾燥して厚さ2μmの保護樹脂層を形成し、その上にア
ルミニウムを真空蒸着法で40nmの厚さに蒸着し、更にそ
の上にスチレンブタジエンゴム10部、塩素化ポリプロピ
レン7部、キシレン樹脂15部をトルエン50部、酢酸エチ
ル50部に溶解してなるコーティング溶液を塗布乾燥し、
厚さ2μmの接着剤層を形成して感熱転写媒体を得た。Comparative Example 2 A coating solution obtained by dissolving 9 parts of paraffin wax and 1 part of ketone resin in a mixed solvent consisting of 70 parts of toluene, 10 parts of turpentine oil and 10 parts of petroleum naphtha was applied onto a 6 μm thick polyester film, followed by drying. 1μm thick
And a coating solution obtained by dissolving 25 parts of a styrene maleic acid resin and 5 parts of an oil dye in a mixed solvent consisting of 30 parts of toluene, 20 parts of methyl isobutyl ketone and 20 parts of cyclohexanone. Is applied and dried to form a protective resin layer having a thickness of 2 μm, and aluminum is deposited thereon to a thickness of 40 nm by a vacuum deposition method. Further, styrene-butadiene rubber 10 parts, chlorinated polypropylene 7 parts, xylene 15 parts of resin 50 parts of toluene, 50 parts of ethyl acetate coating solution consisting of dissolved and dried,
An adhesive layer having a thickness of 2 μm was formed to obtain a thermal transfer medium.
比較例3 厚さ3.5μmのポリエステルフイルム上にアクリル樹
脂20部および塩化ゴム10部をトルエン30部、メチルイソ
ブチルケトン20部およびシクロヘキサノン20部からなる
混合溶剤に溶解して成るコーティング溶液を塗布乾燥し
て厚さ2μmの保護樹脂層を形成し、その上にアルミニ
ウムを真空蒸着法で40nmの厚さに蒸着し、更にその上に
ポリアミド樹脂10部およびカルナバワックス10部をトル
エン70部、イソプロピルアルコール10部からなる混合溶
剤に溶解してなるコーティング溶液を塗布乾燥して厚さ
2μmの接着剤層を形成して感熱転写媒体を得た。Comparative Example 3 A coating solution obtained by dissolving 20 parts of an acrylic resin and 10 parts of a chlorinated rubber in a mixed solvent consisting of 30 parts of toluene, 20 parts of methyl isobutyl ketone and 20 parts of cyclohexanone was applied to a 3.5 μm thick polyester film and dried. A protective resin layer having a thickness of 2 μm is formed thereon, and aluminum is vapor-deposited thereon to a thickness of 40 nm by a vacuum vapor deposition method. Further, 10 parts of a polyamide resin and 10 parts of carnauba wax are further coated with 70 parts of toluene, 70 parts of isopropyl alcohol and A coating solution dissolved in a mixed solvent consisting of 2 parts by weight was applied and dried to form an adhesive layer having a thickness of 2 μm to obtain a thermal transfer medium.
比較例4 厚さ9μmのポリエステルフイルム上にパラフィンワ
ックス9部およびケトン樹脂1部をトルエン70部、テレ
ビン油10部および石油ナフサ10部からなる混合溶剤に溶
解して成るコーティング溶液を塗布乾燥して厚さ1μm
の離型剤層を形成し、次いでその面上にスチレンマレイ
ン酸樹脂25部、および油性染料5部をトルエン30部、メ
チルイソブチルケトン20部およびシクロヘキサノン20部
からなる混合溶剤に溶解して成るコーティング溶液を塗
布乾燥して厚さ2μmの保護樹脂層を形成し、その上に
アルミニウムを真空蒸着法で40nmの厚さに蒸着し、更に
その上にパラフィンワックス20部およびエチレン−酢酸
ビニル共重合樹脂10部をトルエン50部、テレビン油20部
からなる混合溶剤に溶解してなるコーティング溶液を塗
布乾燥して厚さ3μmの接着剤層を構成して感熱転写媒
体を得た。Comparative Example 4 A coating solution obtained by dissolving 9 parts of paraffin wax and 1 part of ketone resin in a mixed solvent consisting of 70 parts of toluene, 10 parts of turpentine oil and 10 parts of petroleum naphtha was applied to a 9 μm-thick polyester film and dried. 1 μm
Is formed by dissolving 25 parts of a styrene-maleic acid resin and 5 parts of an oily dye in a mixed solvent consisting of 30 parts of toluene, 20 parts of methyl isobutyl ketone and 20 parts of cyclohexanone. The solution was applied and dried to form a protective resin layer having a thickness of 2 μm, on which aluminum was vapor-deposited to a thickness of 40 nm by vacuum vapor deposition, and then 20 parts of paraffin wax and an ethylene-vinyl acetate copolymer resin A coating solution prepared by dissolving 10 parts in a mixed solvent consisting of 50 parts of toluene and 20 parts of turpentine oil was applied and dried to form an adhesive layer having a thickness of 3 μm to obtain a thermal transfer medium.
[発明の効果] 実施例1、2および比較例1、2、3、4で得られた
感熱転写媒体を用いて普通紙にパーソナルワードプロセ
ッサ キャノンPW−70(キャノン株式会社製)で印字し
た。[Effects of the Invention] Using the thermal transfer media obtained in Examples 1 and 2 and Comparative Examples 1, 2, 3, and 4, printing was performed on plain paper with a personal word processor Canon PW-70 (manufactured by Canon Inc.).
実施例1および2で得られた本発明の感熱転写媒体を
用いて50sec.以下のラフ紙上に印字した文字画像は極め
て美麗な金属光沢を呈していた。Character images printed on rough paper of 50 sec. Or less using the thermal transfer medium of the present invention obtained in Examples 1 and 2 exhibited extremely beautiful metallic luster.
比較例1〜4で得られた感熱転写媒体を用いて50sec.
以下のラフ紙上に印字した文字画像には、比較例1の場
合のものは熱伝導性が良すぎるため溶融粘度が低く、印
字の際の欠け現象(一般に中抜け、逆転写等と呼ばれて
いる現象)が起こっているのが認められ、比較例2の場
合のものは熱伝導性が悪く高速印字に対応できないばか
りか、分子量が大きいため印字の切れ性(シャープさ)
が悪く印字が不鮮明であり、比較例3および4の場合の
ものはまだ熱伝導性が止すぎるため溶融粘度が低く、印
字の際の欠け現象(一般に中抜け、逆転写等と呼ばれて
いる現象)が起こているのが認められ、その上、分子量
が大きいものが混在するため、印字の切れ性(シャープ
さ)が悪く印字の不鮮明さが認められた。50 seconds using the thermal transfer medium obtained in Comparative Examples 1-4.
In the following character images printed on rough paper, those in Comparative Example 1 had too low thermal viscosity due to too good thermal conductivity, and chipping phenomena during printing (generally referred to as hollowing, reverse transfer, etc.) Phenomenon was observed. In the case of Comparative Example 2, not only the thermal conductivity was poor and it was not possible to cope with high-speed printing, but also the sharpness of the printing due to the large molecular weight.
The prints were poor and the prints were unclear. In the case of Comparative Examples 3 and 4, the thermal conductivity was still too low, the melt viscosity was low, and the chipping phenomenon at the time of printing (generally referred to as hollow, reverse transfer, etc.) Phenomenon) was observed, and in addition, those having a large molecular weight were mixed, so that the sharpness of the print was poor and the print was unclear.
第1図は本願発明の感熱転写媒体の基本構成を示す断面
図である。 (図面の符号) (1):ベースフイルム (2):離型剤層 (3):保護樹脂塗膜層 (4):金属蒸着層 (5):接着剤層 (51):ワックス系分散型接着剤層 (52):溶剤可溶型高分子接着剤層FIG. 1 is a sectional view showing the basic structure of the thermal transfer medium of the present invention. (Signs in the drawings) (1): Base film (2): Release agent layer (3): Protective resin coating layer (4): Metal deposition layer (5): Adhesive layer (51): Wax dispersion type Adhesive layer (52): Solvent-soluble polymer adhesive layer
Claims (1)
を介して、少なくとも保護樹脂塗膜層、金属蒸着層、接
着剤層を順次形成した感熱転写媒体において、接着剤層
がワックス系分散型接着剤層と溶剤可溶型高分子接着剤
層をこの順に積層されてなることを特徴とするラフ紙対
応型感熱転写媒体。1. A heat-sensitive transfer medium in which at least a protective resin coating layer, a metal deposition layer, and an adhesive layer are sequentially formed on a base film directly or via a release agent layer, the adhesive layer has a wax-based dispersion. A rough paper-compatible thermal transfer medium, comprising a lamination type adhesive layer and a solvent-soluble polymer adhesive layer laminated in this order.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62300576A JP2620266B2 (en) | 1987-11-28 | 1987-11-28 | Thermal transfer media |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62300576A JP2620266B2 (en) | 1987-11-28 | 1987-11-28 | Thermal transfer media |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01141086A JPH01141086A (en) | 1989-06-02 |
JP2620266B2 true JP2620266B2 (en) | 1997-06-11 |
Family
ID=17886502
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62300576A Expired - Lifetime JP2620266B2 (en) | 1987-11-28 | 1987-11-28 | Thermal transfer media |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2620266B2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05155160A (en) * | 1991-12-03 | 1993-06-22 | Brother Ind Ltd | Ink ribbon for dry transfer material manufacturing |
JP4080077B2 (en) * | 1998-11-19 | 2008-04-23 | フジコピアン株式会社 | Method for forming metallic gloss image |
FR2800011B1 (en) | 1999-10-22 | 2001-12-07 | Oreal | HOT MARKING METHOD AND MULTI-LAYERED STRUCTURE FOR CARRYING OUT SUCH A METHOD |
-
1987
- 1987-11-28 JP JP62300576A patent/JP2620266B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH01141086A (en) | 1989-06-02 |
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