JPH01108087A - Thermal transfer recording medium - Google Patents
Thermal transfer recording mediumInfo
- Publication number
- JPH01108087A JPH01108087A JP62265996A JP26599687A JPH01108087A JP H01108087 A JPH01108087 A JP H01108087A JP 62265996 A JP62265996 A JP 62265996A JP 26599687 A JP26599687 A JP 26599687A JP H01108087 A JPH01108087 A JP H01108087A
- Authority
- JP
- Japan
- Prior art keywords
- transfer layer
- heat
- transfer
- recording medium
- layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000012546 transfer Methods 0.000 title claims abstract description 121
- 239000000203 mixture Substances 0.000 claims abstract description 48
- 239000012943 hotmelt Substances 0.000 claims description 11
- 238000002844 melting Methods 0.000 claims description 10
- 239000012528 membrane Substances 0.000 claims description 5
- 239000000853 adhesive Substances 0.000 claims description 4
- 230000001070 adhesive effect Effects 0.000 claims description 4
- 239000010410 layer Substances 0.000 abstract description 63
- 239000012790 adhesive layer Substances 0.000 abstract description 17
- 239000011248 coating agent Substances 0.000 abstract description 17
- 238000000576 coating method Methods 0.000 abstract description 17
- 238000007639 printing Methods 0.000 abstract description 13
- 239000000758 substrate Substances 0.000 abstract description 8
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 239000012530 fluid Substances 0.000 abstract description 2
- -1 polyethylene Polymers 0.000 description 12
- 238000009472 formulation Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000001993 wax Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 229920000178 Acrylic resin Polymers 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000007646 gravure printing Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 230000008542 thermal sensitivity Effects 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 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
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 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
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 239000011354 acetal resin Substances 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 229920003020 cross-linked polyethylene Polymers 0.000 description 1
- 239000004703 cross-linked polyethylene Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate 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
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011787 zinc oxide 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
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〉
本発明は感熱プリンターや感熱タイプライタ−に供する
感熱転写記録媒体に関し、より詳しくは多数回使用可能
な感熱転写記録媒体に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a thermal transfer recording medium used in a thermal printer or a thermal typewriter, and more particularly to a thermal transfer recording medium that can be used many times.
〈従来の技術とその問題点〉
従来の感熱溶融型の感熱転写記録媒体は基体フィルム上
に熱溶融性バインダーと着色材からなる熱溶融性転写層
を設けただけの構成のものがほとんどで、次のような欠
点を有している。すなわち、従来この種の記録媒体は、
1回の転写で記録媒体のインキ層が基体フィルム上にほ
とんど残らず、2回目以降の使用では濃度ムラのある印
字物しか得られない、所謂ワンタイム型熱転写シートで
あった。従って、記録を得るためのコストが高くなりだ
、また、1回の印字だけでは感熱転写記録媒体側に印字
の痕跡が明瞭に残存するため、情報の保守面にも問題が
あった。こうした背景から、反専F l 、”]能な感
熱転写記録媒体の検討が進められ従来の反復使用可能な
感熱転写記録媒体においては、基体フィルム上に微細な
多孔’Ill状構造を有する耐熱性樹脂層を設け、その
孔の空げきに熱溶融性インキを含有させて成る感熱転写
材の提案(特開昭55−105579号)がある、この
転写材は感熱ヘッドの発熱体の印加エネルギーの大小に
応じてインキの転写量を制御する手段として注目される
。しかしなゆくら、この記録媒体により印字された画像
品質はワンタイム型の感熱転写記録媒体に比べ掻端に濃
度が低下し、解像度も十分でなく、画像が不鮮明であっ
た。<Prior art and its problems> Most conventional heat-sensitive transfer recording media have a structure in which a heat-melt transfer layer consisting of a heat-melt binder and a coloring material is provided on a base film. It has the following drawbacks. In other words, conventionally, this type of recording medium is
It was a so-called one-time type thermal transfer sheet in which almost no ink layer of the recording medium remained on the base film after one transfer, and only prints with uneven density were obtained after the second use. Therefore, the cost of obtaining a record becomes high, and there is also a problem in terms of information maintenance, since printing only once leaves clear traces of the print on the thermal transfer recording medium. Against this background, studies have been progressing on heat-sensitive transfer recording media that can be used repeatedly. There is a proposal for a thermal transfer material (Japanese Patent Application Laid-Open No. 105579/1983), which has a resin layer and contains hot-melt ink in the pores of the resin layer. It is attracting attention as a means of controlling the amount of ink transferred depending on the size of the ink.However, the quality of the image printed with this recording medium is significantly lower in density than that of a one-time thermal transfer recording medium. The resolution was not sufficient and the image was unclear.
また多数回記録の一つの提案として、基体フィルム上に
多孔膜層上熱溶融性転写層を順次設けた熱転写フィルム
の提案(特開昭60−131296号)がある、この記
録媒体は、1回目の印字品質は濃度、解像度とも、ワン
タイム型の感熱転写記録媒体に相当するという点では優
れているが、印加エネルギーに応じた転写量制御ができ
ず、多数回使用ができない。In addition, as one proposal for multiple recordings, there is a proposal for a thermal transfer film in which a porous film layer and a heat-fusible transfer layer are sequentially provided on a base film (Japanese Patent Application Laid-open No. 131296/1983). Although the printing quality is excellent in terms of both density and resolution and is comparable to that of a one-time type thermal transfer recording medium, it is not possible to control the amount of transfer according to the applied energy, so it cannot be used many times.
〈問題点を解決する為の手段〉
本発明はかかる実情に鑑み、上記の如き感熱転写媒体に
おける従来技術の改善を成さんとするものであり、多数
回使用可能な感熱転写記録媒体の熱感度を向上させ、良
質の画像を提供すると共に、繰り返し寿命に関する特性
を改善した多数回使用可能な感熱転写記録媒体を提供す
ることにある。<Means for Solving the Problems> In view of the above circumstances, the present invention aims to improve the conventional technology of the thermal transfer medium as described above, and improves the thermal sensitivity of the thermal transfer recording medium that can be used many times. It is an object of the present invention to provide a heat-sensitive transfer recording medium that can be used many times and has improved characteristics regarding repeat life, as well as providing high-quality images.
上記目的は、基体上に接着材を介して、貫通孔を存する
多孔膜の前記貫通孔内に熱溶融性組成物が保持されて成
る第1転写層と、熱溶融性組成物から成る第2転写層が
この順に少なくとも積層されており、第1転写層の層厚
は第2転写層の層厚より厚いことを特徴とする感熱転写
記録媒体により達成することができる。The above object is to provide a first transfer layer in which a hot-melt composition is held in the through-holes of a porous membrane having through-holes on a substrate via an adhesive, and a second transfer layer made of a hot-melt composition in the through-holes. This can be achieved by a thermal transfer recording medium characterized in that at least transfer layers are laminated in this order, and the layer thickness of the first transfer layer is thicker than the layer thickness of the second transfer layer.
この記録媒体を使用して感熱記録を行う場合はまず、感
熱転写記録媒体の第2転写層に対面して被転写用紙を配
置した後、押圧媒体により、記録媒体の基体及び被転写
用紙背面双方より押圧し、前記基体′により任意の画像
信号に対応して熱エネルギーを発生させる手段を有した
加熱印字体により、部分的に加熱することで第1及び第
2転写層の熱溶融性組成物を流動化せしめ、第2転写層
から順次、被転写用紙側に熱溶融性組成物を転移させる
。When performing thermal recording using this recording medium, first, the transfer paper is placed facing the second transfer layer of the thermal transfer recording medium, and then a pressure medium is used to press both the base of the recording medium and the back surface of the transfer paper. The heat-melting compositions of the first and second transfer layers are partially heated by a heated printed body having means for generating heat energy from the base body in response to an arbitrary image signal. is fluidized, and the heat-melting composition is sequentially transferred from the second transfer layer to the transfer paper side.
以下、本発明をより明瞭にならしむるため、図面を参照
しつつ詳細に説明する。Hereinafter, in order to make the present invention more clear, the present invention will be described in detail with reference to the drawings.
第1図及び第2図は本発明の感熱転写記録媒体の構成例
の概略断面説明図である。第1図及び第2図に示すよう
に、感熱転写記録媒体1及びIBは各々、基体2上に接
着層3を介して、貫通孔有する多孔M6.6Bの前記貫
通孔内に熱溶融性組成物7゜7Bを保持させた第1転写
層4.4Bを設け、更にその上に、ワックス、着色剤、
結着剤、油類等より構成される第2転写層5を積層した
感熱転写記録媒体であり、第1転写層4.4Bの塗布厚
みが第2転写層5の塗布厚みより厚くなっている。第1
転写層は多数回使用の為に、1度で転写する熱溶融性組
成物量を制御できるようにするためのものでありまた、
第2転写層は、少なくとも1回目の印字が低エネルギー
で行なえ、高解像度の画像が形成できるようにするため
のものである。多孔膜6及び6Bは、各々、第2転写層
5まで貫通した独立孔や二次元網状に貫通した連通孔を
存している。FIGS. 1 and 2 are schematic cross-sectional views of an example of the structure of a thermal transfer recording medium of the present invention. As shown in FIGS. 1 and 2, each of the thermal transfer recording media 1 and IB has a heat-fusible composition in the through-holes of the M6.6B through-holes on the base 2 via the adhesive layer 3. A first transfer layer 4.4B holding the object 7゜7B is provided, and wax, colorant,
It is a thermal transfer recording medium in which a second transfer layer 5 made of a binder, oil, etc. is laminated, and the coating thickness of the first transfer layer 4.4B is thicker than the coating thickness of the second transfer layer 5. . 1st
The transfer layer is intended to be used many times, so that the amount of the hot-melt composition transferred at one time can be controlled.
The second transfer layer is provided so that at least the first printing can be performed with low energy and a high resolution image can be formed. The porous films 6 and 6B each have independent holes that penetrate to the second transfer layer 5 and communicating holes that penetrate in a two-dimensional network.
基体2は、熱伝導性の高い緻密で薄く平滑な媒体であり
、熱溶融性転写層を保持し、熱溶融性組成物7の基体2
背面8への漏洩を防ぎ、加熱印字体等への汚染を防ぐた
めのもので、従来公知の基体が用いられる。−例をあげ
れば、ポリエチレンポリプロピレン、ポリエチレンテレ
フタート、ボリイミ゛ド、アラミド等の高分子フィルム
、あるいはコンデンサーペーパー、ラミネート紙、コー
ト紙等の薄葉紙状のものであり、感熱記録時における熱
応答性、更に機械的強度を考慮した場合、2〜15(μ
m)の厚みのものが好適であるがこれに限定はされない
、更に、接着層3と対面し、加熱印字体等と接する基体
2の背面8に耐熱性処理が施してあってもよい。The substrate 2 is a dense, thin, and smooth medium with high thermal conductivity that holds the heat-melt transfer layer and transfers the heat-melt composition 7 to the base 2.
This is to prevent leakage to the back surface 8 and contamination of the heated printed material, etc., and a conventionally known substrate is used. - Examples include polymer films such as polyethylene polypropylene, polyethylene tereftate, polyimide, and aramid, or thin paper materials such as condenser paper, laminated paper, and coated paper. Furthermore, when mechanical strength is taken into account, 2 to 15 (μ
A thickness of m) is preferable, but the thickness is not limited to this.Furthermore, the back surface 8 of the base 2 facing the adhesive layer 3 and in contact with the heated printed body etc. may be subjected to a heat-resistant treatment.
基体2と第1転写層4.4Bの間には接着層3が設けで
あるが、これは第1転写FJ4.4Bの基体2からの剥
離を防止するための効果がある。接着層3の厚さは0.
1〜5(μl1))の範囲で設定することが可能である
が、熱感度、接着強度を考慮した場合0.3〜2(μl
1))の範囲で用いることが好ましい。An adhesive layer 3 is provided between the substrate 2 and the first transfer layer 4.4B, and this has the effect of preventing the first transfer FJ 4.4B from peeling off from the substrate 2. The thickness of the adhesive layer 3 is 0.
It is possible to set it in the range of 1 to 5 (μl 1), but when considering thermal sensitivity and adhesive strength, it is 0.3 to 2 (μl
It is preferable to use within the range of 1)).
接着層3に用いる具体的な材料として、ポリエチレン、
架橋ポリエチレン、塩素化ポリエチレン、エチレン−酢
酸ビニル共重合体、ポリエチレンテレフタレート、ポリ
プロピレン、ポリイソブチレン、ポリ塩化ビニル、ポリ
塩化ビニリデン、ポリ酢酸ビニル、ポリビニルアルコー
ル、ポリビニルアセタール、ふっ素樹脂、アクリル樹脂
、ポリアクリスタリン、ポリスチレン、アセタール樹脂
ポリアミド、ポリカーボネート、セルロース系プラスチ
ック、スチレン−アクリロニトリル共重合体、アクリロ
ニトリル−ブタジェン−スチレン三元共重合体、フェノ
ール樹脂、ユリア樹脂、エボシキ樹脂、不飽和ポリエス
テル樹脂、アクリル酸エステル系樹脂、アルキド樹脂、
メラミン樹脂、ケイ素樹脂、ポリウレタン、ジアリルフ
タレート樹脂、ポリフェニレンオキサイド、ポリイミド
、ポリスルホン、塩化ゴム、塩酸ゴム、環化ゴム、ポリ
イソプレン、ポリブタジェン、スチレン−ブタジェン共
重合体、ポリクロロプレン、ニトリルゴム、ブチルゴム
、アクリルゴム、エチレン−プロピレンゴム等があり、
これらのうちから1種或いは2種以上を組み合わせて使
用すればよい、上記の接着層3はホットメルトコーティ
ング、ソルベントコーチインク或いはエマルシランコー
ティング等の塗布手段を用いて形成することができる。Specific materials used for the adhesive layer 3 include polyethylene,
Cross-linked polyethylene, chlorinated polyethylene, ethylene-vinyl acetate copolymer, polyethylene terephthalate, polypropylene, polyisobutylene, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polyvinyl alcohol, polyvinyl acetal, fluororesin, acrylic resin, polyacrystalline, Polystyrene, acetal resin polyamide, polycarbonate, cellulose plastic, styrene-acrylonitrile copolymer, acrylonitrile-butadiene-styrene terpolymer, phenol resin, urea resin, eboshiki resin, unsaturated polyester resin, acrylic ester resin, alkyd resin,
Melamine resin, silicone resin, polyurethane, diallyl phthalate resin, polyphenylene oxide, polyimide, polysulfone, chlorinated rubber, hydrochloric acid rubber, cyclized rubber, polyisoprene, polybutadiene, styrene-butadiene copolymer, polychloroprene, nitrile rubber, butyl rubber, acrylic rubber, ethylene-propylene rubber, etc.
One type or a combination of two or more of these may be used. The adhesive layer 3 described above can be formed using coating means such as hot melt coating, solvent coach ink, or emulsion silane coating.
接着層3の上に設けられた第1転写層4.4B及び第2
転写N5に用いられる熱溶融性組成物としては従来公知
のものがそのまま用いられ、ワックス、着色剤、結着剤
、油類等より構成される。The first transfer layer 4.4B and the second transfer layer 4.4B provided on the adhesive layer 3
As the heat-melting composition used for transfer N5, conventionally known compositions can be used as they are, and are composed of wax, colorant, binder, oil, and the like.
着色剤としては、例えば顔料系でいえば黒色の場合はカ
ーボンブラック、オイルブラック等を用いることが出来
、カラーの場合にはベンジンイエロー、ローダミンレー
キB、フタロシニアンブルー等の通常のものを用いるこ
とが出来る。勿論、用途により染料を用いることも特に
規定はされるものではない、ワックス類としては、例え
ばパラフィンワックス、マイクロクリスタリンワックス
、カルナバワックス、モンタンワックス、木ろう、みつ
ろう、低分子量ポリエチレンワックス、合成ワックス等
が用いられる。結着剤としてはエチレ7−ff酸エチル
共重合体、エチレン−酢酸ビニル共重合体、ポリアミド
樹脂、ロジン系誘導体、石油樹脂、アクリル樹脂、ポリ
エステル樹脂等が用いられる。油類としては鉱油、植物
油等が用いられる。As a colorant, for example, in the case of pigment-based black, carbon black, oil black, etc. can be used, and in the case of color, ordinary ones such as benzine yellow, rhodamine lake B, phthalocyanine blue, etc. can be used. I can do it. Of course, there is no particular restriction on the use of dyes depending on the purpose. Examples of waxes include paraffin wax, microcrystalline wax, carnauba wax, montan wax, wood wax, beeswax, low molecular weight polyethylene wax, synthetic wax, etc. is used. As the binder, ethyl 7-ff acid copolymer, ethylene-vinyl acetate copolymer, polyamide resin, rosin derivative, petroleum resin, acrylic resin, polyester resin, etc. are used. Mineral oil, vegetable oil, etc. are used as the oil.
第2転写層5は着色剤等を前記バインダーに適宜、混合
、分散処理を施し、ホットメルト型、溶剤型或いは水性
型インキと成し、グラビア法やロールコータ法、フレキ
ソ印刷法を用いて第1転写層4.4B上に形成する。The second transfer layer 5 is formed by suitably mixing and dispersing a coloring agent and the like in the binder to form a hot-melt, solvent-based, or water-based ink, which is then printed using a gravure method, a roll coater method, or a flexographic printing method. 1 is formed on the transfer layer 4.4B.
第2転写層5の塗布量は、必要とする発色濃度にも依存
するが、実用的なエネルギー感度の面から、0.1〜1
0g/rdの範囲に設定することが可、能であるが、高
解像度、高濃度の画像を期待する場合には、2〜5g/
n(の塗布量が好ましい。The coating amount of the second transfer layer 5 depends on the required coloring density, but in terms of practical energy sensitivity, the coating amount is 0.1 to 1.
It is possible to set it in the range of 0 g/rd, but if you expect high resolution and high density images, set it in the range of 2 to 5 g/rd.
A coating amount of n( is preferred.
−力筒1転写ji4.4Bの塗布量は必要とする繰り返
し数にも依存するが、実用的なエネルギー感度の面から
0.2〜20g/rrfの範囲に設定することが可能で
あり、3回以上の繰り返しを行ない、高解像度の画像を
期待する場合には3〜10g/イの塗布量が好しい。こ
こで、第1転写F3i 4.4Bの塗布厚みを第2転写
層5の塗布厚みより大きく設定することで、本発明の効
果、即ち、従来の提案に比べ低い印字エネルギーの高品
位多数回記録を最大限に活かすことが可能となる。第1
転写層464Bの多孔1)!6.68−t−構成する要
素として、耐熱温度が100°C以上の高分子が好しく
、熱可塑型或いは熱硬化型のポリ酢酸ビニル、塩化ビニ
ル−酢酸ビニル共重合体、ポリビニルプチール、アクリ
ル樹脂、ポリアミド、アクリロニトリル−塩化ビニル共
重合体、セルロース系プラスチック、ポリエステル、ポ
リウレタン、合成ゴム及びこれらの混合物等を用いるこ
とができる。印刷或いは塗工適性の向上及び見かけの耐
熱性向上のため、構成成分として炭酸カルシウム、酸化
チタン、酸化ケイ素、酸化亜鉛、カーボン等の顔料粒子
を含んでも良く、適切な溶媒、非溶媒又は貧溶媒を洗濯
することによりスラリー状態を呈する組成物を用いるこ
が可能である。- The amount of coating of force cylinder 1 transfer ji4.4B depends on the number of repetitions required, but from the standpoint of practical energy sensitivity, it can be set in the range of 0.2 to 20 g/rrf, and 3 When repeating the application more than once and expecting a high-resolution image, a coating amount of 3 to 10 g/i is preferable. Here, by setting the coating thickness of the first transfer layer F3i 4.4B to be larger than the coating thickness of the second transfer layer 5, the effect of the present invention can be achieved, that is, high-quality multiple recording with lower printing energy than conventional proposals. It is possible to make the most of it. 1st
Pores in transfer layer 464B 1)! 6.68-t-The constituent elements are preferably polymers with a heat resistance temperature of 100°C or higher, such as thermoplastic or thermosetting polyvinyl acetate, vinyl chloride-vinyl acetate copolymer, polyvinyl butyl, Acrylic resin, polyamide, acrylonitrile-vinyl chloride copolymer, cellulose plastic, polyester, polyurethane, synthetic rubber, and mixtures thereof can be used. In order to improve suitability for printing or coating and to improve apparent heat resistance, pigment particles such as calcium carbonate, titanium oxide, silicon oxide, zinc oxide, carbon, etc. may be included as constituent components, and an appropriate solvent, non-solvent or poor solvent may be used. It is possible to use a composition that exhibits a slurry state by washing.
第1転写層4.4Bは、例えば、前記熱溶融性組成物と
多孔膜用高分子スラリーを適宜、混合分散処理を施し、
溶剤型インキと成し、グラビア法やロールコータ法、フ
レキソ印刷法を用いて接着層3の上に形成する。The first transfer layer 4.4B is formed by, for example, appropriately mixing and dispersing the hot-melt composition and a polymer slurry for a porous membrane,
It is made of a solvent-based ink and is formed on the adhesive layer 3 using a gravure method, a roll coater method, or a flexographic printing method.
このように、本発明の多数回使用可能な感熱転写記録媒
体は基体上に接着N3を塗工後、多孔膜用の高分子6.
6Bと熱溶融性組成物7,7Bの混合物スラリ−を塗工
して第1転写層4.4Bを形成した後、第2転写層5を
積層して得られる。As described above, the thermal transfer recording medium of the present invention, which can be used many times, is coated with adhesive N3 on the substrate, and then coated with polymer 6.
After forming the first transfer layer 4.4B by coating a slurry of a mixture of 6B and the hot-melt compositions 7 and 7B, the second transfer layer 5 is laminated.
次に、かくして得られた少なくとも四層構成より成る感
熱転写記録゛媒体を用い、熱転写記録方法の一実施例を
図面に添って説明する。Next, an embodiment of a thermal transfer recording method using the thus obtained thermal transfer recording medium having at least four layers will be described with reference to the drawings.
まず、第3図に示すように、先に例示した如き感熱転写
記録媒体1の第2転写層5に対面して被転写用紙18を
配置した後、加熱印字体9と圧力ローラー1)間に挿入
し、加圧状態に保つ、しかる後、電源部10により発生
した信号を電気回路を経て加熱印字体9に伝えて、発熱
させ、その接触箇所にある熱溶融性組成物12を基体2
を部分的に伝播させた熱により流動化させ、更に強い押
圧ものもとで変形させ、多孔膜6の細孔を通して押し出
し、被転写用紙18に到達させる。しかる後、感熱転写
記録媒体1と被転写用紙18を搬送ローラ一部13−a
。First, as shown in FIG. 3, after placing the transfer paper 18 facing the second transfer layer 5 of the thermal transfer recording medium 1 as exemplified above, the paper 18 is placed between the heated printing body 9 and the pressure roller 1). After that, a signal generated by the power supply unit 10 is transmitted to the heated print body 9 via an electric circuit to generate heat, and the heat-melting composition 12 at the contact point is transferred to the base 2.
is fluidized by partially propagated heat, deformed under stronger pressure, pushed out through the pores of the porous membrane 6, and reached the transfer paper 18. After that, the thermal transfer recording medium 1 and the transfer paper 18 are conveyed by the conveying roller part 13-a.
.
13−bにおいて剥離すると転写画像12aを得ること
が出来る。By peeling off at step 13-b, a transferred image 12a can be obtained.
次に多数回使用の原理を第4図にて説明する。Next, the principle of multiple use will be explained with reference to FIG.
第4図において、加熱印字体及び加圧ローラーは省略し
であるが、その位置関係は第3図に従う。In FIG. 4, the heated printed body and the pressure roller are omitted, but their positional relationship is as shown in FIG. 3.
第4図において12−1.12−2.12−3は順に感
熱転写記録媒体の同一位置を同一エネルギーで印字し、
繰り返し数が増加した際、成された転写形態を模式図的
に便宜的に説明しである。まず、加熱印字体により加熱
された第1転写層4内熱溶融性組成物7、及び第2転写
層5の熱溶融性組成物の12−1部分は一様に流動状態
となり、加圧されながら被転写用紙18に転写される。In FIG. 4, 12-1, 12-2, 12-3 print in the same position on the thermal transfer recording medium with the same energy,
The transfer form achieved when the number of repetitions increases is schematically explained for convenience. First, the heat-melt composition 7 in the first transfer layer 4 and the heat-melt composition 12-1 in the second transfer layer 5 that have been heated by the heated printing body uniformly become fluid and are pressurized. The image is transferred onto the transfer paper 18 while the image is being transferred.
第2転写層5の熱溶融性組成物の転写原理は従来公知の
ワンタイム型のシートと同じであり、普通紙(コピー用
紙程度の祇)にも高濃度、高解像度の印字像12−It
が得られる。The transfer principle of the heat-melting composition of the second transfer layer 5 is the same as that of conventionally known one-time type sheets, and a high density, high resolution printed image 12-It can be printed even on plain paper (about the same size as copy paper).
is obtained.
12−2部分では、すでに第2転写層5の熱溶融性組成
物がほとんど消費され、第2転写層4の熱溶融性組成物
7が加熱及び加圧により細孔を伝わって被転写用紙18
に転写される様子を示している。更に数回繰り返し数が
増加した12−3部分では、多孔膜6の細札内に充填さ
れていた熱溶融性組成物までも被転写用紙18に移行し
、感熱転写記録媒体1の12−3部分の熱溶融性組成物
はほとんど消費され、熱溶融性組成物が効率的に無駄な
く使用できることを示している。In the portion 12-2, most of the heat-melting composition of the second transfer layer 5 has already been consumed, and the heat-melting composition 7 of the second transfer layer 4 is transferred through the pores by heating and pressure to the transfer paper 18.
This shows how it is transferred to. In the 12-3 portion where the number of repetitions is further increased several times, even the heat-melting composition filled in the thin strip of the porous film 6 is transferred to the transfer paper 18, and the 12-3 portion of the thermal transfer recording medium 1 is transferred to the transfer paper 18. Most of the hot-melt composition was consumed, indicating that the hot-melt composition can be used efficiently and without waste.
〈発明の効果〉
本発明による感熱転写記録媒体は以上のような構成であ
るため、従来のワンタイム型の転写記録媒体に比べ、多
数回の使用が可能であり、かつ従来の多数回使用型の感
熱転写記録体の提案よりも低エネルギーの印加で高品位
、高解像度画像を得ることが可能となった。<Effects of the Invention> Since the thermal transfer recording medium according to the present invention has the above-described structure, it can be used many times compared to conventional one-time type transfer recording media, and can be used more times than conventional one-time type transfer recording media. It has become possible to obtain high-quality, high-resolution images with lower energy application than the proposed thermal transfer recording material.
〈実施例〉
以下、本発明の実施例及び比較例を述べる。なお、本発
明はこれらの実施例に限定されるものでなく、この発明
の技術思想を逸脱しない範囲で種々の変形が可能である
。<Examples> Examples and comparative examples of the present invention will be described below. Note that the present invention is not limited to these embodiments, and various modifications can be made without departing from the technical idea of the present invention.
〈実施例1〉
6.0(μm)厚の承すエチレンテレフタートフィルム
の上にグラビアロールコータを用いて処方Aで示す接着
層用塗液をソルベント塗工し、乾燥膜厚が1.0(μm
)の接着層を設けた。<Example 1> On a 6.0 (μm) thick ethylene tereftate film, a coating liquid for an adhesive layer shown in formulation A was solvent coated using a gravure roll coater, and the dry film thickness was 1.0. (μm
) was provided with an adhesive layer.
(処方A)
エチレン−酢酸ビニル共重合体・・・・・・5重量部(
ダイヤボンド工業社製)
トルエン ・・・・・・95重量部
更に処方Bにて示すパラフィンワックスを主成分とする
熱溶融性組成物及びアクリル樹脂を主成分とする多孔膜
構成用組成物をリニアーミル分散機にて混合分散し、第
2転写層用インキを作成し、グラビア印刷法にて上記接
着層の上に塗工して10μ霧の第1転写層を設けた。(Formulation A) Ethylene-vinyl acetate copolymer...5 parts by weight (
(manufactured by Diabond Kogyo Co., Ltd.) Toluene: 95 parts by weight Furthermore, a hot-melt composition containing paraffin wax as a main component and a composition for forming a porous film containing an acrylic resin as a main component shown in Formulation B were processed in a linear mill. The ink for the second transfer layer was prepared by mixing and dispersing using a dispersing machine, and the ink for the second transfer layer was coated on the adhesive layer using a gravure printing method to provide a first transfer layer with a mist of 10 μm.
(処方B)
ワックスエマルジョン #3o7・・・・・・50ff
ifi部(ボンドワックス株式会社製)
エマコールブラック D−305・・・・・・10重量
部(三陽色素株式会社) ・・・・・・40重量部
アクリルエマルジョン ブライマル HA−16(ロー
ム・アンド・ジャパン株式会社)・・・・・・40重量
部
次いで処方Cにて示す水性型のエマルジョンインキを上
記第1転写層の上に塗工して4μmの第2転写層を設け
、本発明の感熱転写記録媒体を得た。(Formulation B) Wax emulsion #3o7...50ff
ifi part (manufactured by Bond Wax Co., Ltd.) Emacol Black D-305 10 parts by weight (Sanyo Shiki Co., Ltd.) 40 parts by weight Acrylic emulsion Brimal HA-16 (ROHM & Co., Ltd.)・Japan Co., Ltd.)...40 parts by weight of the water-based emulsion ink shown in Formulation C was then coated on the first transfer layer to form a second transfer layer of 4 μm. A thermal transfer recording medium was obtained.
(処方C)
ワックスエマルジョン #307・・・・・・80重量
部(ボンドワックス株式会社)
エマコールブラック D−305・・・・・・20重量
部(三陽色素株式会社)
この感熱転写記録媒体と十条製紙株式会社製熱転写用祇
をハンディ−ワードプロセッサー(日本電気株式会社製
、文豪m1ni3E)にセットし、記録媒体の同一箇所
を使用してベタ印字を繰り返し、評価した。印字速度は
高品質モード、印字電圧は中位モードとした。次に、反
射濃度をサクラ濃度計P[1A−65(小西六写真工業
社製)で測定した。その結果、第1表に示すように濃度
低下の少ない印字を6回行なうことができた。また汚れ
も無く、印字品質も良好であった。(Formulation C) Wax emulsion #307...80 parts by weight (Bond Wax Co., Ltd.) Emacol Black D-305...20 parts by weight (Sanyo Shiki Co., Ltd.) This thermal transfer recording medium A thermal transfer paper manufactured by Jujo Paper Industries Co., Ltd. was set in a handy word processor (Bungo m1ni3E manufactured by NEC Corporation), and solid printing was repeatedly performed using the same location on the recording medium for evaluation. The printing speed was set to high quality mode, and the printing voltage was set to medium mode. Next, the reflection density was measured using a Sakura densitometer P[1A-65 (manufactured by Konishiroku Photo Industry Co., Ltd.). As a result, as shown in Table 1, it was possible to print six times with little decrease in density. There was also no stain and the print quality was good.
〈実施例2〉
6.0(μm)厚のポリエチレンテレフタートフィルム
の上にグラビアロールコータを用いて、処方りで示す接
着層用塗液をソルベント塗工し、乾燥膜厚が1.0 μ
閘の接着層を設けた。<Example 2> On a polyethylene tereftate film with a thickness of 6.0 (μm), a gravure roll coater was used to solvent-coat the adhesive layer coating liquid shown in the recipe, and the dry film thickness was 1.0 μm.
An adhesive layer for the lock was provided.
(処方D)
ウレタン樹脂
(大日本インキ社製) ・・・・・・5重量部トル
エン ・・・・・・951i1部更
に処方Eにて示す第1転写層用インキ組成物を実施例1
と同様に混合、分散し、グラビア印刷法にて上記接着層
の上に塗工して10μ−の第1転写層を設けた。(Formulation D) Urethane resin (manufactured by Dainippon Ink Co., Ltd.) 5 parts by weight Toluene 1 part 951i Further, the ink composition for the first transfer layer shown in Formulation E was prepared in Example 1
The mixture was mixed and dispersed in the same manner as above, and coated on the adhesive layer using a gravure printing method to form a 10 μm first transfer layer.
(処方E)
セルロースアセテートプロピオネート
(住友バイエルウレタン株式会社製)
・・・・・・10重量部
メチルエチルケトン ・・・・・・53重量部
ワックスエマルジョン #307・・・・・・3o重を
部(ボンドワックス株式会社製)
エマコールブラック D−305・・・・・・7重量部
次いで、処方Cにて示す第1転写層用インキを実施例1
と同様に塗工し、本発明の感熱転写記録媒体を得た。(Formulation E) Cellulose acetate propionate (manufactured by Sumitomo Bayer Urethane Co., Ltd.) 10 parts by weight Methyl ethyl ketone 53 parts by weight Wax emulsion #307 3 parts by weight (manufactured by Bond Wax Co., Ltd.) Emacol Black D-305...7 parts by weight Next, ink for the first transfer layer shown in Formulation C was used in Example 1.
Coating was carried out in the same manner as above to obtain a thermal transfer recording medium of the present invention.
この感熱転写記録媒体を実施例1と同様に評価したとこ
ろ、表1に示すように、良好な繰り返し特性を得た。This thermal transfer recording medium was evaluated in the same manner as in Example 1, and as shown in Table 1, good repeatability characteristics were obtained.
く比較例1〉
市販の繰り返し可能な転写リボン(松下電器産業株式会
社製、CF−KPR132K )を実施例1と同様に評
価した。Comparative Example 1 A commercially available repeatable transfer ribbon (CF-KPR132K, manufactured by Matsushita Electric Industrial Co., Ltd.) was evaluated in the same manner as in Example 1.
表1に示すように、第1回目から十分な濃度が得られず
、基体フィルム面からのインキ剥落ちが観察された。As shown in Table 1, a sufficient density could not be obtained from the first time, and ink peeling from the surface of the base film was observed.
【図面の簡単な説明】
図面は本発明の実施例を示すもので、第1図は本発明に
係る感熱転写記録媒体の概略断面説明図、第2図は他の
例の感熱転写記録媒体の概略断面説明図、第3図は本発
明の感熱転写記録媒体を用いた記録方法を現わす断面説
明図、第4図は第2図に示した記録媒体を用いた場合の
記録原理を現わす断面説明図をそれぞれ示す。
1.1B ・・・感熱転写記録媒体
2 ・・・基体 3 ・・・接着層4.4B
・・・第1転写屡 5 ・・・第2転写層6.6B
・・・多孔膜 7.7B ・・・熱溶融性組成
物時 許 出 願 人
凸版印刷株式会社
代表者 鈴木和夫
第1図
78 6B[BRIEF DESCRIPTION OF THE DRAWINGS] The drawings show examples of the present invention, and FIG. 1 is a schematic cross-sectional view of a thermal transfer recording medium according to the present invention, and FIG. 2 is a schematic cross-sectional view of a thermal transfer recording medium according to another example. A schematic cross-sectional explanatory diagram; FIG. 3 is a cross-sectional explanatory diagram showing the recording method using the thermal transfer recording medium of the present invention; FIG. 4 is a cross-sectional explanatory diagram showing the recording principle when the recording medium shown in FIG. 2 is used. A cross-sectional explanatory diagram is shown respectively. 1.1B...Thermal transfer recording medium 2...Substrate 3...Adhesive layer 4.4B
...First transfer layer 5 ...Second transfer layer 6.6B
... Porous membrane 7.7B ... Heat-melting composition Applicant: Toppan Printing Co., Ltd. Representative Kazuo Suzuki Figure 1 78 6B
Claims (1)
の前記貫通孔内に熱溶融性組成物が保持されて成る第1
転写層と、熱溶融性組成物から成る第2転写層がこの順
に少なくとも積層されており、第1転写層の層厚は第2
転写層の層厚より厚いことを特徴とする感熱転写記録媒
体。(1) A first composition comprising a porous membrane having through-holes with a hot-melt composition held in the through-holes on the base via an adhesive.
At least a transfer layer and a second transfer layer made of a heat-melting composition are laminated in this order, and the thickness of the first transfer layer is equal to the thickness of the second transfer layer.
A thermal transfer recording medium characterized by being thicker than a transfer layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62265996A JPH01108087A (en) | 1987-10-21 | 1987-10-21 | Thermal transfer recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62265996A JPH01108087A (en) | 1987-10-21 | 1987-10-21 | Thermal transfer recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01108087A true JPH01108087A (en) | 1989-04-25 |
Family
ID=17424917
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62265996A Pending JPH01108087A (en) | 1987-10-21 | 1987-10-21 | Thermal transfer recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01108087A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60234890A (en) * | 1984-05-09 | 1985-11-21 | Konishiroku Photo Ind Co Ltd | Thermal transfer recording medium |
JPS62121090A (en) * | 1985-11-21 | 1987-06-02 | Ricoh Co Ltd | Thermal transfer recording medium |
JPS62158087A (en) * | 1985-12-29 | 1987-07-14 | Ricoh Co Ltd | Thermal transfer recording medium |
-
1987
- 1987-10-21 JP JP62265996A patent/JPH01108087A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60234890A (en) * | 1984-05-09 | 1985-11-21 | Konishiroku Photo Ind Co Ltd | Thermal transfer recording medium |
JPS62121090A (en) * | 1985-11-21 | 1987-06-02 | Ricoh Co Ltd | Thermal transfer recording medium |
JPS62158087A (en) * | 1985-12-29 | 1987-07-14 | Ricoh Co Ltd | Thermal transfer recording medium |
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