JPH01258984A - Thermal transfer sheet - Google Patents
Thermal transfer sheetInfo
- Publication number
- JPH01258984A JPH01258984A JP63085310A JP8531088A JPH01258984A JP H01258984 A JPH01258984 A JP H01258984A JP 63085310 A JP63085310 A JP 63085310A JP 8531088 A JP8531088 A JP 8531088A JP H01258984 A JPH01258984 A JP H01258984A
- Authority
- JP
- Japan
- Prior art keywords
- thermal transfer
- heat
- transfer sheet
- ink layer
- network structure
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000010410 layer Substances 0.000 claims abstract description 37
- 239000000463 material Substances 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims abstract description 18
- 238000002844 melting Methods 0.000 claims abstract description 15
- 239000002344 surface layer Substances 0.000 claims abstract description 7
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 238000007639 printing Methods 0.000 abstract description 16
- 229920006015 heat resistant resin Polymers 0.000 abstract description 9
- 239000003086 colorant Substances 0.000 abstract description 8
- 239000012943 hotmelt Substances 0.000 abstract description 7
- 229920000728 polyester Polymers 0.000 abstract description 7
- 230000008018 melting Effects 0.000 abstract description 5
- 239000002985 plastic film Substances 0.000 abstract description 4
- 229920006255 plastic film Polymers 0.000 abstract description 4
- 239000000758 substrate Substances 0.000 abstract 2
- 238000010030 laminating Methods 0.000 abstract 1
- 238000010186 staining Methods 0.000 abstract 1
- 239000000976 ink Substances 0.000 description 32
- 239000001993 wax Substances 0.000 description 17
- 239000012188 paraffin wax Substances 0.000 description 12
- -1 polypropylene Polymers 0.000 description 12
- 238000000576 coating method Methods 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 5
- 239000003431 cross linking reagent Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229920005992 thermoplastic resin Polymers 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000004203 carnauba wax Substances 0.000 description 4
- 235000013869 carnauba wax Nutrition 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000007646 gravure printing Methods 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229940081735 acetylcellulose Drugs 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 239000001023 inorganic pigment Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000004200 microcrystalline wax Substances 0.000 description 2
- 235000019808 microcrystalline wax Nutrition 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- KVUYSIIZYQUVMT-UHFFFAOYSA-N 1,2-diisothiocyanatoethane Chemical compound S=C=NCCN=C=S KVUYSIIZYQUVMT-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000004163 Spermaceti wax Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 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
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 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
- 229910000019 calcium carbonate Inorganic materials 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
- 239000003990 capacitor Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229940015043 glyoxal Drugs 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
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001083 polybutene 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
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000012176 shellac wax Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000019385 spermaceti wax Nutrition 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000007651 thermal printing Methods 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene 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
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/38278—Contact thermal transfer or sublimation processes using ink-containing structures, e.g. porous or microporous layers, alveoles or cellules
-
- 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
- B41M5/41—Base layers supports or substrates
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は熱転写シートの改良に関し、更に詳しくは一般
的熱転写方法及び被転写材の搬送速度を熱転写シートの
搬送速度よりも大として行う熱転写方法(以下弔にN倍
そ−ド法という)において熱溶融性インキ層による被転
写紙の地汚れを防止することのできる熱転写シートに関
する。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to improvements in thermal transfer sheets, and more specifically to a general thermal transfer method and a thermal transfer method in which the conveyance speed of the transfer material is higher than the conveyance speed of the thermal transfer sheet. The present invention relates to a thermal transfer sheet that can prevent background smearing of transfer paper due to a layer of heat-melting ink in a thermal transfer sheet (hereinafter referred to as the N-fold method).
(従来の技術及びその問題点)
従来、コンピューターやワードプロセッサーの出カブリ
ントを熱転写方式によって印字する場合には、基材フィ
ルムの一方の面に熱溶融性インキ層を設けた熱転写シー
トが使用されている。(Prior art and its problems) Conventionally, when printing output prints from computers or word processors using a thermal transfer method, a thermal transfer sheet with a heat-melting ink layer provided on one side of a base film has been used. .
この従来の熱転写シートは、基材フィルムとして厚さ1
0乃至20μmのコンデンサ紙やパラフィン紙のような
紙或いは厚さ3乃至20μmのポリエステルやセロファ
ンのようなプラスチックのフィルムを用い、ワックスに
顔料や染料等の着色剤を混合した熱溶融性インキ層をコ
ーティングにより設けて製造したものである。This conventional thermal transfer sheet has a thickness of 1 mm as a base film.
Using paper such as capacitor paper or paraffin paper with a thickness of 0 to 20 μm, or a plastic film such as polyester or cellophane with a thickness of 3 to 20 μm, a layer of heat-melting ink made by mixing coloring agents such as pigments and dyes with wax is applied. It is manufactured by coating.
従来の熱転写シートを用いて被転写紙に出カブリントす
ると、インキ層が被転写紙面に直接に接触し、両者の摩
擦によって非印字部に地汚れが発生することが多かった
。When a conventional thermal transfer sheet is used to print on a transfer paper, the ink layer comes into direct contact with the transfer paper surface, and the friction between the two often causes scumming in non-print areas.
又、N倍モード方法では、被転写材の搬送速度をNとし
、熱転写シートの搬送速度をN′とし、NUN ′とす
ると、印字距離はNでありながら、熱転7fシートの消
費距離がN′となることから、印字距離に対する熱転写
シートの消費量が節約できるという利点があるか、被転
写材と熱転写シートとが常に相対的に移動して摩擦され
るため、形成される印字はこすられて字汚れが発生し、
又、印字は糸引き状になり、印字濃度も低く、印字品位
か劣るという問題がある。In addition, in the N-times mode method, if the conveyance speed of the transfer material is N, the conveyance speed of the thermal transfer sheet is N', and NUN', the printing distance is N, but the consumption distance of the thermal transfer 7f sheet is N. ′, there is an advantage in that the amount of thermal transfer sheet consumed relative to the printing distance can be saved, or because the transfer material and the thermal transfer sheet are constantly moving relative to each other and are rubbed, the printed characters are not rubbed. The letters are smudged,
In addition, there are problems in that the print becomes stringy, the print density is low, and the print quality is poor.
本発明は上述の事情を付置にして為されたものであり、
その目的は例えN倍モード法で熱転写を行っても地汚れ
や糸引きが発生せず、鮮明な印字を与えることができる
熱転写シートを提供することである。The present invention has been made in consideration of the above-mentioned circumstances,
The purpose is to provide a thermal transfer sheet that does not cause scumming or stringiness even when thermal transfer is performed using the N-times mode method, and can provide clear prints.
(問題点を解決するための手段) 上記目的は以下の本発明によって達成される。(Means for solving problems) The above objects are achieved by the present invention as described below.
すなわち、本発明は、基材フィルムの一方の面に、熱溶
融性インキ層と表面層とが形成された熱転写シートであ
って、前記表面層が耐熱性網目構造を有することを特徴
とする熱転写シートであ(作 用)
熱溶融性インキ層トに耐熱性の網LI Jul¥造を形
成することによって、N倍モード法においても被転′す
材の地汚れ及び印字の糸引き現象か解決される。That is, the present invention provides a thermal transfer sheet in which a heat-melting ink layer and a surface layer are formed on one side of a base film, wherein the surface layer has a heat-resistant network structure. (Function) By forming a heat-resistant net on the heat-melting ink layer, it is possible to solve the problem of background smearing on the rolled material and stringy printing even in the N-time mode method. be done.
(好ましい実施態様)
次に好ましい実施態様により本発明を更に詳しく説明す
る。(Preferred Embodiments) Next, the present invention will be explained in more detail with reference to preferred embodiments.
本発明の熱転写シートは、基材フィルムの一方の表面に
熱溶融性インキ層を形成し、史にその上に網目構造の表
面層を形成したものである。The thermal transfer sheet of the present invention has a heat-melting ink layer formed on one surface of a base film, and a network-structured surface layer formed thereon.
本発明で用いられる基材フィルムとしては、従来の熱転
写シートに使用されていると同じ基材フィルムがそのま
ま用いることができると共に、その他のものも使用する
ことができ、特に制限されない。As the base film used in the present invention, the same base film used in conventional thermal transfer sheets can be used as is, and other films can also be used, and there are no particular limitations.
好ましい基材フィルムの具体例としては、例えば、ポリ
エステル、ポリプロピレン、セロハン、ポリカーボネー
ト、酢酸セルロース、ポリエチレン、ポリ塩化ビニル、
ポリスチレン、ナイロン、ポリイミド、ポリ塩化ビニリ
デン、ポリビニルアルコール、フッ素樹脂、塩化ゴム、
アイオノマー等のプラスチック、コンデンサー紙、パラ
フィン紙等の紙類、不織布等があり、又、これらを複合
した基材フィルムであってもよい。Specific examples of preferred base films include polyester, polypropylene, cellophane, polycarbonate, cellulose acetate, polyethylene, polyvinyl chloride,
Polystyrene, nylon, polyimide, polyvinylidene chloride, polyvinyl alcohol, fluororesin, chlorinated rubber,
Examples include plastics such as ionomers, papers such as condenser paper and paraffin paper, nonwoven fabrics, and base films made of composites of these materials.
この基材フィルムの厚さは、その強度及び熱伝導性か適
切になるように材料に応じて適宜変更することができる
が、その厚さは、好ましくは、例えば、2乃至25μm
である。The thickness of this base film can be changed as appropriate depending on the material so that its strength and thermal conductivity are appropriate, but the thickness is preferably, for example, 2 to 25 μm.
It is.
上記基材フィルム上に形成する熱溶融性インキ層は、着
色剤とビヒクルとからなり、更に必要に応して種々の添
加剤を加えたものでもよい。The heat-melting ink layer formed on the base film comprises a colorant and a vehicle, and may further contain various additives as necessary.
この着色剤としては、有機又は無機の顔料若しくは染料
のうち、記録材料として良好な特性を有するもの、例え
ば、十分な着色濃度を有し、光、熱、温度等により変褪
色しないものが好ましい。The coloring agent is preferably an organic or inorganic pigment or dye that has good properties as a recording material, for example, one that has sufficient color density and does not discolor or fade due to light, heat, temperature, etc.
又、非加熱時には無色であるが加熱時に発色するものや
、被転写体に塗布されているものと接触することにより
発色するような物質でもよい。シアン、マゼンタ、イエ
ロー、ブラックを形成する着色剤の外に、他の種々の色
の着色剤をも用いることができる。これらの着色剤の使
用量はインキ中で約2乃至90重量%を占める使用割合
が一般的に好ましい。Further, it may be a substance that is colorless when not heated but develops color when heated, or a substance that develops color when it comes into contact with something coated on the transfer target. In addition to the colorants forming cyan, magenta, yellow, and black, colorants of various other colors can also be used. It is generally preferred that these colorants be used in an amount of about 2 to 90% by weight in the ink.
ビヒクルとしては、ワックスを主成分とし、その他ワッ
クスと乾性油、樹脂、鉱油、セルロース及びゴムの誘導
体等との混合物が用いられる。The vehicle used includes wax as a main component, and mixtures of wax with drying oil, resin, mineral oil, cellulose, rubber derivatives, and the like.
ワックスの代表例としては、マイクロクリスタリンワッ
クス、カルナバワックス、パラフィンワックス等がある
。更に、フィッシャートロプシュワックス、各種低分子
L1ポリエチレン、木ロウ、ミツロウ、鯨ロウ、イポタ
ロウ、羊毛ロウ、セラックワックス、キャンデリラワッ
クス、ペトロラクタム、ポリエステルワックス、一部変
性ワックス、脂肪酸エステル、脂肪酸アミド等線々のワ
ックスが用いられる。Representative examples of wax include microcrystalline wax, carnauba wax, paraffin wax, and the like. Furthermore, Fischer-Tropsch wax, various low-molecular L1 polyethylenes, wood wax, beeswax, spermaceti wax, ipotal wax, wool wax, shellac wax, candelilla wax, petrolactam, polyester wax, partially modified waxes, fatty acid esters, fatty acid amides, etc. Various waxes are used.
基材フィルム上にインキ層を形成する方法としては、ホ
ットメルトコートの外、ホットラッカーコート、グラビ
アコート、グラビアリバースコート、ロールコートその
他多くの手段等が挙げられる。Methods for forming the ink layer on the base film include hot melt coating, hot lacquer coating, gravure coating, gravure reverse coating, roll coating, and many other methods.
本発明では更に上記インキ層中に比較的低融点の熱可塑
性樹脂を混合して、形成されるインキ層の被転写材に対
する接着性を向上させることができる。このような熱可
塑性樹脂としては、例えば、エチレン−酢酸ビニル共重
合体(EVA)、エチレン−アクリル酸エステル共重合
体(EE八)、ポリエチレン、ポリスチレン、ポリプロ
ピレン、ポリブテン、石油樹脂、塩化ビニル樹脂、塩化
ビニル−酢酸ビニル共重合体、ポリビニルアルコール、
塩化ビニリデン樹脂、メタクリル樹脂、ポリアミド、ポ
リカーボネート、フッ素樹脂、ポリビニルフォルマール
、ポリビニルブチラール、アセチルセルロース、ニトロ
セルロース、ポリ酢酸ビニル、ポリイソブチレン、エチ
ルセルロース、ポリウレタン又はポリアセタール等が用
いられ、特に従来感熱接着剤として使用されている比較
的低軟化点、例えば、50乃至80℃の軟化点を有する
ものが好ましい。ワックスと熱可塑性樹脂との使用割合
は、ワックス100に対して熱可塑性樹脂が5乃至30
0である重量比の範囲が好ましい。In the present invention, a thermoplastic resin having a relatively low melting point may be further mixed into the ink layer to improve the adhesion of the formed ink layer to the transfer material. Examples of such thermoplastic resins include ethylene-vinyl acetate copolymer (EVA), ethylene-acrylic acid ester copolymer (EE8), polyethylene, polystyrene, polypropylene, polybutene, petroleum resin, vinyl chloride resin, Vinyl chloride-vinyl acetate copolymer, polyvinyl alcohol,
Vinylidene chloride resin, methacrylic resin, polyamide, polycarbonate, fluororesin, polyvinyl formal, polyvinyl butyral, acetyl cellulose, nitrocellulose, polyvinyl acetate, polyisobutylene, ethyl cellulose, polyurethane or polyacetal are used, especially as conventional heat-sensitive adhesives. It is preferred that those used have a relatively low softening point, for example a softening point of 50 to 80°C. The ratio of wax and thermoplastic resin used is 5 to 30 parts thermoplastic resin to 100 parts wax.
A weight ratio range of 0 is preferred.
上記インキ層の表面に形成する耐熱性網目構造は、熱転
写時の熱によって溶融しない網目構造であり、インキ層
よりも高い融点を有し且つインキ層と相溶しない耐熱性
樹脂材料から形成する。このような耐熱性樹脂の1例と
しては水溶性乃至親水性の樹脂、例えば、ポリビニルア
ルコール、ポリ酢酸ビニルの部分鹸化物、ポリビニルピ
ロリドン、ポリアクリル酸、ヒドロキシエチルセルロー
ス、カルボキシメチルセルロース、水溶性ポリエステル
、水溶性ポリアミド、水溶性ポリウレタン等が挙げられ
る。これらの樹脂は水溶性乃至親水性であるので架橋す
ることなく(勿論架橋させることも好ましい)疎水性の
高いワックスとは相溶することがない。The heat-resistant network structure formed on the surface of the ink layer is a network structure that does not melt due to heat during thermal transfer, and is formed from a heat-resistant resin material that has a higher melting point than the ink layer and is incompatible with the ink layer. Examples of such heat-resistant resins include water-soluble or hydrophilic resins, such as polyvinyl alcohol, partially saponified polyvinyl acetate, polyvinylpyrrolidone, polyacrylic acid, hydroxyethylcellulose, carboxymethylcellulose, water-soluble polyester, and water-soluble Examples include water-soluble polyamide and water-soluble polyurethane. Since these resins are water-soluble or hydrophilic, they are not crosslinked (of course crosslinking is also preferred) and are not compatible with highly hydrophobic waxes.
別の例の耐熱性樹脂としては架橋性或いは熱硬化性の耐
熱性樹脂が挙げられる。例えば、従来塗料及び印刷イン
キの分野で使用されているような種々の耐熱性樹脂が使
用できる。これらの耐熱性樹脂は多孔層の形成時又は形
成後に架橋剤の添加や加熱によって硬化させて、ワック
スに対して十分に非相溶性とすることができる。架橋剤
としては、ポリイソシアネート、メチロール化合物、エ
ポキシ化合物、ポリアミン、メラミン樹脂、グリオキザ
ール樹脂等が使用される。Another example of the heat resistant resin includes a crosslinkable or thermosetting heat resistant resin. For example, various heat resistant resins can be used, such as those conventionally used in the paint and printing ink fields. These heat-resistant resins can be cured by adding a crosslinking agent or by heating to make them sufficiently incompatible with wax during or after forming the porous layer. As the crosslinking agent, polyisocyanate, methylol compound, epoxy compound, polyamine, melamine resin, glyoxal resin, etc. are used.
以上の如き樹脂を用いて適当なインキを調製し、これを
眞記熱溶融性インキ層上にグラビア印刷等により網目状
に印刷し、乾燥することによって網目構造が形成できる
。A network structure can be formed by preparing a suitable ink using the above-mentioned resin, printing it in a network shape by gravure printing or the like on the heat-melting ink layer, and drying it.
他の好ましい方法としては、上記樹脂をバインダーとし
てこの中に適当な粒子や短繊維を添加して層を形成する
方法であり、例えば、シリカ、アルミナ、タルク、クレ
ー、ケイソウ土、炭酸カルシウム、硫酸バリウム等の種
々の無機顔料、エポキシ樹脂、アクリル樹脂、尿素樹脂
、メラミン樹脂、ポリエチレン、ポリプロピレン等の樹
脂からなるプラスチックピグメント或いは上記の如き無
機材料及び有機材料からなる各J11短繊維、ポリエス
テル、ポリアミド、ポリアクリロニトリル、木綿等の短
繊維等の充填剤を加えたインキを使用する方法である。Another preferred method is to form a layer by using the above resin as a binder and adding appropriate particles or short fibers therein, such as silica, alumina, talc, clay, diatomaceous earth, calcium carbonate, sulfuric acid, etc. Various inorganic pigments such as barium, plastic pigments made of resins such as epoxy resins, acrylic resins, urea resins, melamine resins, polyethylene and polypropylene, or J11 short fibers made of inorganic and organic materials such as those mentioned above, polyester, polyamide, This method uses ink containing fillers such as polyacrylonitrile and short fibers such as cotton.
上記充填剤とバインダーとから層を形成するに当り、バ
インダーの量を多く使用すれば、網目構造は形成できな
いが、バインダーの量を少なくすることによって種々の
空隙率を有する網目構造を形成することができる。例え
ば、充填剤の粒子径によっである程度変化するが、粒子
100容量部に対しバインダーの川を10乃至400容
■部、好ましくは100乃至200容量部とすることに
よって種々の空隙率の網目構造が形成される。勿論、上
記充填剤を含むインキはグラビア印刷等により網目状に
印刷して網目構造を形成してもよい。When forming a layer from the above-mentioned filler and binder, if a large amount of binder is used, a network structure cannot be formed, but by reducing the amount of binder, a network structure with various porosity can be formed. I can do it. For example, although this varies to some extent depending on the particle size of the filler, network structures with various porosity can be created by adding 10 to 400 parts by volume, preferably 100 to 200 parts by volume, of the binder per 100 parts by volume of the particles. is formed. Of course, the ink containing the filler may be printed in a mesh shape by gravure printing or the like to form a network structure.
以上の如き網目構造の空隙率は面積比で1%程度から9
9%程度まで任意に形成できるが、本発明においてはl
O乃至80%程度の空隙率を有するのが良く、空隙率が
上記範囲未満であると、熱転写時のインキの排出量が少
なくなり、一方、空隙率が上記範囲を越えると、網「1
構造自体の強度が不足し、熱転写時に破壊さねたりして
好ましくない。The porosity of the network structure as described above ranges from about 1% to 9% in terms of area ratio.
Although it can be formed arbitrarily up to about 9%, in the present invention, l
It is preferable to have a porosity of about 0 to 80%. If the porosity is less than the above range, the amount of ink discharged during thermal transfer will be small, while if the porosity exceeds the above range, the net
The structure itself lacks strength and may break during thermal transfer, which is undesirable.
以上のように形成される網[1構造は高速タイプのプリ
ンターのように印字エネルギーが低くなる場合も感度不
足とならないように、この層の厚さは本発明において、
好ましくは0.1μm以上5μm未満である。この厚さ
が0.1μm未満では、被転写紙とインキ層とがこすれ
て地汚れを生じる恐れがある。上記網目構造は実質的に
無着色であり、Amの体質顔料や白色顔料を加えて白色
には着色してもよい。In the present invention, the thickness of this layer is set so that the net structure formed as described above does not lack sensitivity even when the printing energy is low as in a high-speed printer.
Preferably it is 0.1 μm or more and less than 5 μm. If the thickness is less than 0.1 μm, there is a risk that the transfer paper and the ink layer will rub against each other, resulting in scumming. The network structure is substantially uncolored, and may be colored white by adding an extender pigment of Am or a white pigment.
基旧フィルムに熱にsンい材料を用いる場合、サーマル
ヘッドに接する側の表面に、サーマルヘッドのスティッ
キングを防止する層を設けることが好ましい。スティッ
キング防+h層は、耐熱性のある樹脂と熱離型剤又は滑
剤の働きをする物質とを基本的な構成成分とする。耐熱
性のある樹脂としては、ガラス転移点が60℃以上の合
成樹脂又はOH基又はC0OH基を有する熱可塑性樹脂
にアミノ基を2個以トイfする化合物又はジイソシアネ
ート若しくは1へジイソシアネートを加えて若干の架橋
硬化を起させたものが好適である。熱離型剤又は滑剤は
、ワックス類や高級脂肪酸のアミド、エステル及び塩の
ような加熱に3にり溶融してその作用をするものと、フ
ッ素樹脂や無機物質の粉末のように固体のままで役)γ
つものとがある。When a heat-resistant material is used for the base film, it is preferable to provide a layer on the surface in contact with the thermal head to prevent sticking of the thermal head. The basic components of the anti-sticking +h layer include a heat-resistant resin and a substance that functions as a heat release agent or a lubricant. Heat-resistant resins include synthetic resins with a glass transition point of 60°C or higher, thermoplastic resins having OH groups or COOH groups, and compounds containing two or more amino groups, or diisocyanates, or diisocyanates added to 1 and a little. It is preferable to use a material that undergoes crosslinking and curing. Thermal mold release agents or lubricants include those that melt when heated, such as waxes, amides, esters, and salts of higher fatty acids, and those that remain solid, such as fluororesin and inorganic substance powders. role) γ
There is always something.
このようなスティッキング防市層を設けることによって
、熱に弱いプラスチックフィルムを基材とした熱転写シ
ートにおいてもスティッキングが起こることなく熱印字
が可能であって、プラスチックフィルムの持つ切れにく
さ、加工のし易さ等のメリットが生かせる。By providing such a sticking layer, it is possible to perform thermal printing without causing sticking even on thermal transfer sheets based on heat-sensitive plastic films, and it is possible to print thermally without sticking, and to reduce the difficulty of cutting and processing of plastic films. Benefits such as ease of use can be taken advantage of.
本発明をカラー印字用の熱転写シートに適用できること
はいうまでもないから、多色の熱転写シートも又本発明
の範囲に含まれる。又、熱転写プリンターとしてはライ
ン或はシリアルタイプのいずれにも適用することができ
る。Since it goes without saying that the present invention can be applied to thermal transfer sheets for color printing, multicolor thermal transfer sheets are also included within the scope of the present invention. Further, as a thermal transfer printer, it can be applied to either a line or serial type.
(効 果)
以上の如き本発明によれば、熱溶融性インキ層上に、網
目構造を形成することによって、N倍モート法において
も被転写材の地汚れ及び印字の糸引き現象が解決された
。(Effects) According to the present invention as described above, by forming a network structure on the heat-fusible ink layer, the background smudge on the transfer material and the stringy print phenomenon can be solved even in the N-times mote method. Ta.
すなわち、インキ層上に網目構造が存在することによっ
て、熱転写時の被転写材と熱転写シートかこすられても
、網目構造は無色又は白色であるのて被転写材は汚染さ
れない。That is, due to the presence of the network structure on the ink layer, even if the transfer material and the thermal transfer sheet are rubbed during thermal transfer, the transfer material will not be contaminated because the network structure is colorless or white.
そして、サーマルヘッドから十分な熱が供給された時(
印字時)のみ溶融インキが網目構造から噴出されるので
地汚れのない明瞭な印字が可能である。又、多孔層の空
隙率を大にしておくことによりN倍モードで熱転写して
も印字濃度が低下することもない。Then, when sufficient heat is supplied from the thermal head (
Since molten ink is ejected from the network structure only during printing, clear printing without background smearing is possible. Furthermore, by increasing the porosity of the porous layer, the print density will not decrease even if thermal transfer is performed in the N-fold mode.
(実施例) 以下、実施例を挙げて本発明を更に具体的に説明する。(Example) Hereinafter, the present invention will be explained in more detail with reference to Examples.
尚、文中、部又は%とあるのは特に断りのない限り重量
基準である。In the text, parts or percentages are based on weight unless otherwise specified.
実施例I
Hさ3.5μmのポリエチレンテレフタレートのフィル
ムを基材フィルムとし、その一方の面に下記の組成の熱
溶融性インキ層及び網]」構造用材料とを夫々付記した
手段により塗布及び乾燥して本発明の熱転写シートを得
た。Example I A polyethylene terephthalate film with a height of 3.5 μm was used as a base film, and on one side thereof, a heat-melting ink layer and a net with the following composition and a “structural material” were coated and dried by the means indicated respectively. A thermal transfer sheet of the present invention was obtained.
悲庇改作ヱ之ま尤
カーボンブラック(ダイヤブラックG、三菱化成製)
15部エチレン/酢酸ビニ
ル共重合体(V、V八ツレックス31O1三井ポリケミ
カル製) 8部パラフィンワックス(パラフィン1
5叶、11本錆蝋製) 50部カ
ルナバワックス 25部アトライター
を用いて、120℃で6時間混練したものを、インキ温
度120℃のホットメルトロールコート法により、5g
/rn”(乾燥状態)の割合で塗布した。Kaikou adaptation Enoma Yu Carbon Black (Diablack G, manufactured by Mitsubishi Kasei)
15 parts ethylene/vinyl acetate copolymer (V, V Eighturex 31O1 manufactured by Mitsui Polychemicals) 8 parts paraffin wax (paraffin 1
(5 leaves, 11 pieces made of rust wax) 50 parts carnauba wax 25 parts Attritor was kneaded at 120°C for 6 hours, and 5g was mixed by hot melt roll coating at an ink temperature of 120°C.
/rn'' (dry state).
射■構童
熱硬化性アクリル樹脂 50部架橋剤
1部触媒
0.1部溶剤
160部グラビア方式でIg/m″の割合で網目印刷し
、60℃で1時間乾燥させ、更に50℃で24時間熟成
した。この層の空隙率は面積比で76%であった。Thermosetting acrylic resin 50 parts Crosslinking agent
1 part catalyst
0.1 part solvent
Mesh printing was performed at a ratio of Ig/m'' using a 160-part gravure method, dried at 60° C. for 1 hour, and further aged at 50° C. for 24 hours. The porosity of this layer was 76% in terms of area ratio.
1−記の熱転写シートを用い、被転写紙として上質紙を
使用し、市販のサーマルヘッドを使用して熱転写印字を
行った。サーマルヘッドのエネルギー0.7W/ドツト
で、被転写紙の搬送速度(N)400m/秒、熱転写シ
ートの搬送速度(N′)20cm/秒で、N/N ’=
2のN倍モートで高速印字を行ったところ、地汚れ及び
印字の糸引のない高品質の印字が実施できた。Thermal transfer printing was performed using the thermal transfer sheet described in 1- above, using high-quality paper as the transfer paper, and using a commercially available thermal head. When the energy of the thermal head is 0.7 W/dot, the conveying speed of the transfer paper (N) is 400 m/sec, and the conveying speed of the thermal transfer sheet (N') is 20 cm/sec, N/N'=
When high-speed printing was performed at N times mode of 2, high-quality printing was achieved without background smearing or stringy printing.
実施例2
実施例1と同じ基材フィルムを用い、下記の組成の材料
を使用し、他は実施例1と同様にして本発明の熱転写シ
ートを得た。Example 2 A thermal transfer sheet of the present invention was obtained in the same manner as in Example 1 except that the same base film as in Example 1 was used and the materials having the following composition were used.
愁症敵性42ま届
カーボンブラック(ダイヤブラックG、三菱化成製)
15部エチレン/酢酸ビニル
共重合体(14V八フレツクス31O1三井ポリケミカ
ル製) EBISパラフィンワックス(パラフィ
ン15叶、日本精蝋製) 5
0部カルナバワックス 25部アトラ
イターを用いて、120℃で6時間混練したものを、イ
ンキ温度120℃ホットメルトロールコート法により6
.5g/m″(乾燥状態)の割合で塗11i L/た。42 minute carbon black (dia black G, manufactured by Mitsubishi Kasei)
15 parts ethylene/vinyl acetate copolymer (14V Hachiflex 31O1 manufactured by Mitsui Polychemicals) EBIS paraffin wax (paraffin 15 leaves, manufactured by Nippon Seiro) 5
0 parts carnauba wax 25 parts Using an attritor, the mixture was kneaded at 120°C for 6 hours, and then mixed with an ink temperature of 120°C using a hot melt roll coating method.
.. 11i L/m was applied at a rate of 5 g/m'' (dry state).
新旦構L
プラスチックピグメント(粒子径約3.5μm、エポキ
シ樹脂粒子) 50部反応性ポリエステル樹
脂 15部架橋剤
1部触媒 0.1部
溶剤 160部グラビアコー
ターで乾燥時4μmの厚みに塗工し、60℃で1時間乾
燥させ、更に50℃で24時間熟成した。この層の空隙
率は面積比で68%であった。Shindankaku L Plastic pigment (particle size: approx. 3.5 μm, epoxy resin particles) 50 parts Reactive polyester resin 15 parts Crosslinking agent
1 part catalyst 0.1 part solvent 160 parts Coated to a dry thickness of 4 μm using a gravure coater, dried at 60° C. for 1 hour, and further aged at 50° C. for 24 hours. The porosity of this layer was 68% in area ratio.
この転写シートも、実施例1と同様に良好な転写性能を
示しだ。This transfer sheet also showed good transfer performance as in Example 1.
実施例3
実施例1と同じ基材フィルムを用い、下記の組成の材料
を使用し、他は実施例1と同様にして本発明の熱転写シ
ートを得た。Example 3 A thermal transfer sheet of the present invention was obtained in the same manner as in Example 1 except that the same base film as in Example 1 was used and the materials having the following composition were used.
悠直鑓性イ2先届
カーボンブラック(ダイヤブラックG、三菱化成製)
15部エチレン/酢酸ビニ
ル共重合体(EVAフレックス31O1三井ポリケミカ
ル製) 8部パラフィンワックス(パラフィン15
0F、日本精蝋製) 50部
カルナバワックス 25部アトライタ
ーを用いて、120℃で6時間混練したものを、インキ
温度120℃ホットメルトロールコート法により8.0
g/m″(乾燥状態)の割合で塗布した。Easy-to-use carbon black (dia black G, manufactured by Mitsubishi Kasei)
15 parts ethylene/vinyl acetate copolymer (EVA Flex 31O1 manufactured by Mitsui Polychemicals) 8 parts paraffin wax (paraffin 15
0F, manufactured by Nippon Seiro) 50 parts carnauba wax 25 parts Attritor was kneaded at 120°C for 6 hours, and the ink temperature was 8.0° by hot melt roll coating at 120°C.
g/m'' (dry state).
狙且構L
ポリエステル短繊維(径0.5μm、長さ10μm)
50部エポキシ樹脂
20部架橋剤
1部触媒 0.1部溶剤
160部グラビアコータ
ーで乾燥時2μmの厚みに塗工し、60℃で1時間乾燥
させ、更に50℃で24時間熟成した。この層の空隙率
は面積比で70%であった。Aim and Structure L Polyester short fiber (diameter 0.5 μm, length 10 μm)
50 parts epoxy resin
20 parts crosslinking agent
1 part catalyst 0.1 part solvent 160 parts It was coated using a gravure coater to a dry thickness of 2 μm, dried at 60° C. for 1 hour, and further aged at 50° C. for 24 hours. The porosity of this layer was 70% in area ratio.
この例の転写シートも、地汚れもなく良好な転写性能を
示した。The transfer sheet of this example also exhibited good transfer performance without background stains.
実施例4
厚さ6μmのポリエチレンテレフタレートフィルムをベ
ースイフイルムとして用い、イエロー(Y)、マゼンタ
(M)、シアン(C)及びブラック(B)の各色の熱溶
融性インキ及び網目構造用インキを用いて実施例1と同
様にして本発明の熱転写シートをIB7だ。Example 4 A polyethylene terephthalate film with a thickness of 6 μm was used as a base film, and hot-melt inks and network structure inks of each color of yellow (Y), magenta (M), cyan (C), and black (B) were used. In the same manner as in Example 1, a thermal transfer sheet of the present invention was prepared as IB7.
悠症融立ヱ2A光
顔料(イエロー、マゼンタ、シアン又はブラックの顔料
)。 4部エチレン/酢酸ビニル
共屯合体くスミテートK(ニー10 、住人化学工業製
) 7.5部酸化パラフィンエステル系複合化合
物(アミドポリマーT−820、電化ポリマー製)12
.5部
パラフィンワックス(パラフィン5P−0145、「1
本精蝋製) 15部マイクロク
リスタリンワックス(ハイミック2065、日本績!l
fi製) 10部イソプロパツール
5部キシレン
46部上記4色のインキ組成物を用いてグラビア印
刷法により、イエロー、マゼンタ、シアン及びブラック
の順に面順次に印刷した。その時の塗工重量は6g/m
’(乾燥時)であった。Yukyo Yuryu E2A light pigment (yellow, magenta, cyan or black pigment). 4 parts ethylene/vinyl acetate conjugate sumitate K (Nie 10, produced by Sumitomo Chemical Co., Ltd.) 7.5 parts oxidized paraffin ester composite compound (amide polymer T-820, produced by Denka Polymer) 12
.. 5 parts paraffin wax (paraffin 5P-0145, "1
Made of genuine wax) 15 parts Microcrystalline wax (HIMIC 2065, Nihon Kei! l
manufactured by fi) 10 parts isopropanol
5 parts xylene
46 parts Yellow, magenta, cyan, and black were printed in the order of surface sequentially by a gravure printing method using the above four-color ink compositions. The coating weight at that time was 6g/m
' (when dry).
狙■構竜
アクリル系紫外線硬化性塗料
グラビア印刷方式にてIg/m″の割合で網目印刷及び
光硬化させた。この層の空隙率は面積比で60%であっ
た。The acrylic ultraviolet curable paint was printed with a mesh at a rate of Ig/m'' using a gravure printing method and photocured.The porosity of this layer was 60% in terms of area ratio.
以上の工程により作成した本発明の熱転写シートを使用
し、N/N′=1.7のN倍モードでカラーサーマルプ
リンターで印字を行ったところ、紙とフィルムがこすら
れて生じる地汚れが全くなかった。When the thermal transfer sheet of the present invention prepared by the above process was used to print with a color thermal printer in N-times mode with N/N' = 1.7, there was no background smear caused by rubbing the paper and film. There wasn't.
特許出願人 大日本印刷株式会社Patent applicant: Dai Nippon Printing Co., Ltd.
Claims (3)
表面層とが形成された熱転写シートであって、前記表面
層が耐熱性網目構造を有することを特徴とする熱転写シ
ート。(1) A thermal transfer sheet comprising a heat-melting ink layer and a surface layer formed on one side of a base film, wherein the surface layer has a heat-resistant network structure.
で熱転写を行う際に、被転写材の搬送速度を熱転写シー
トの搬送速度よりも大とする熱転写方法に使用する請求
項1に記載の熱転写シート。(2) Thermal transfer according to claim 1, which is used in a thermal transfer method in which the conveying speed of the transferred material is higher than the conveying speed of the thermal transfer sheet when the thermal transfer sheet and the transferred material are overlapped and thermal transfer is performed with a thermal head. sheet.
1に記載の熱転写シート。(3) The thermal transfer sheet according to claim 1, wherein the network structure is formed from a crosslinkable resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63085310A JPH01258984A (en) | 1988-04-08 | 1988-04-08 | Thermal transfer sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63085310A JPH01258984A (en) | 1988-04-08 | 1988-04-08 | Thermal transfer sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01258984A true JPH01258984A (en) | 1989-10-16 |
Family
ID=13855030
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63085310A Pending JPH01258984A (en) | 1988-04-08 | 1988-04-08 | Thermal transfer sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01258984A (en) |
-
1988
- 1988-04-08 JP JP63085310A patent/JPH01258984A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH0229517B2 (en) | ||
JPS6342592B2 (en) | ||
JPH0355319B2 (en) | ||
JPS62121091A (en) | Thermal transfer sheet | |
JPS62261486A (en) | Thermal transfer recording sheet | |
JPH01258984A (en) | Thermal transfer sheet | |
JPH09202058A (en) | Thermal ink transfer sheet | |
JP2686610B2 (en) | Manufacturing method of thermal transfer sheet | |
JPH0238470A (en) | Ink composition and its production | |
JPH023387A (en) | Multiple printing thermal transfer sheet | |
JPH01214479A (en) | Thermal transfer sheet | |
JPH09272265A (en) | Thermal transfer sheet | |
JPH03114783A (en) | Thermal transfer sheet | |
GB2273992A (en) | Thermal transfer sheet | |
JPH01228887A (en) | Wax composition and heat transfer sheet | |
JP2880283B2 (en) | Thermal transfer sheet | |
JP2700554B2 (en) | Thermal transfer sheet | |
JPH04126283A (en) | Multi-time printing thermal transfer sheet | |
JP2958063B2 (en) | Thermal transfer sheet | |
JPH0238468A (en) | Ink composition and its production | |
JPH044186A (en) | Thermal transfer sheet | |
JPH01214477A (en) | Thermal transfer sheet | |
JPH03197092A (en) | Thermal transfer sheet | |
JPH01295890A (en) | Thermal transfer image receiving sheet and thermal transferring method | |
JPS61258789A (en) | Thermal transfer sheet |