JPS62189195A - Thermal transfer recording sheet - Google Patents
Thermal transfer recording sheetInfo
- Publication number
- JPS62189195A JPS62189195A JP61042846A JP4284686A JPS62189195A JP S62189195 A JPS62189195 A JP S62189195A JP 61042846 A JP61042846 A JP 61042846A JP 4284686 A JP4284686 A JP 4284686A JP S62189195 A JPS62189195 A JP S62189195A
- Authority
- JP
- Japan
- Prior art keywords
- thermal transfer
- transfer sheet
- image
- receiving layer
- styrene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 86
- 229920005989 resin Polymers 0.000 claims abstract description 65
- 239000011347 resin Substances 0.000 claims abstract description 65
- 239000000203 mixture Substances 0.000 claims abstract description 38
- 229920001577 copolymer Polymers 0.000 claims abstract description 25
- 239000000178 monomer Substances 0.000 claims abstract description 12
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims abstract description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 6
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims abstract description 5
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims abstract description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229920001519 homopolymer Polymers 0.000 claims abstract description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000000463 material Substances 0.000 claims description 40
- 229920001296 polysiloxane Polymers 0.000 claims description 18
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 12
- 238000004040 coloring Methods 0.000 claims description 8
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 8
- -1 acrylic ester Chemical class 0.000 claims description 7
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 claims description 5
- 239000006082 mold release agent Substances 0.000 claims description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 4
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 239000004927 clay Substances 0.000 claims description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000011787 zinc oxide Substances 0.000 claims description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 claims 2
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 229920000058 polyacrylate Polymers 0.000 claims 1
- 229920000193 polymethacrylate Polymers 0.000 claims 1
- 125000005396 acrylic acid ester group Chemical group 0.000 abstract 1
- 229920002545 silicone oil Polymers 0.000 description 25
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
- 239000000975 dye Substances 0.000 description 14
- 238000005562 fading Methods 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 12
- 238000000576 coating method Methods 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 239000000123 paper Substances 0.000 description 9
- 238000001035 drying Methods 0.000 description 6
- 238000007639 printing Methods 0.000 description 6
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 6
- 238000001514 detection method Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229920006267 polyester film Polymers 0.000 description 4
- 238000000859 sublimation Methods 0.000 description 4
- 230000008022 sublimation Effects 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 239000002216 antistatic agent Substances 0.000 description 3
- 239000000986 disperse dye Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 239000012463 white pigment Substances 0.000 description 3
- 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 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 229920000896 Ethulose Polymers 0.000 description 2
- 239000001859 Ethyl hydroxyethyl cellulose Substances 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 2
- 229920000638 styrene acrylonitrile Polymers 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 241001330002 Bambuseae Species 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 229920003314 Elvaloy® Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 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
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 229920001890 Novodur Polymers 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 208000028659 discharge Diseases 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- ULYZAYCEDJDHCC-UHFFFAOYSA-N isopropyl chloride Chemical compound CC(C)Cl ULYZAYCEDJDHCC-UHFFFAOYSA-N 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000011088 parchment paper Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 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
- 238000009877 rendering Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 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
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は被熱転写シートに関し、詳しくは画像情報に応
じて熱転写シートの色材層中の昇華染料を加熱転写せし
めて画像記録を行うための被熱転写シートに関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a thermal transfer sheet, and more specifically, a sheet for recording an image by thermally transferring a sublimation dye in a coloring material layer of a thermal transfer sheet according to image information. The present invention relates to a thermal transfer sheet.
近年、CRTディスプレイ上の画像より直接写真のよ・
うな画像を記録するための記録方式として、電気信号に
よって発熱が制御されるサールマヘッド笠によって熱転
写シートを加熱し、熱転写シートの色材層中の昇華性染
料を′I&熱転写シー1〜上に転写せしめて画像情報の
記録を行う熱転写記録方式が採用されている。この熱転
写記録方式は、シアン、マゼンタ、イエローの重ね記録
を行うことによって、色の濃淡に連続的な変化を有する
カラー画像を転写記録することができる方式として注H
されている。上記熱転写記録方式において用いられる被
熱転写シートとして、従来は基材の表面にポリエテル樹
脂を塗布し、昇華性染料が転写される受像層を形成した
ものが用いられている。In recent years, it has become possible to use photographs directly from images on CRT displays.
As a recording method for recording such an image, the thermal transfer sheet is heated by a thermal head cap whose heat generation is controlled by an electric signal, and the sublimable dye in the color material layer of the thermal transfer sheet is transferred onto 'I & thermal transfer sheet 1~. A thermal transfer recording method is adopted in which image information is recorded using This thermal transfer recording method is a method that can transfer and record color images with continuous changes in color shading by overlapping recording of cyan, magenta, and yellow.
has been done. Conventionally, the thermal transfer sheet used in the thermal transfer recording method is a sheet in which a polyether resin is applied to the surface of a base material to form an image-receiving layer to which a sublimable dye is transferred.
しかしながら、従来の被熱転写シー1−では転写された
画像の耐光性が悪く、保管中に転写された画像の鮮明度
が低下し、長期間に亘って美麗な画像を維持できない欠
点があった。これはザーマルヘソドによって短時間にエ
ネルギーを印加して染料を昇華転写せしめる昇華転写法
では、染料が被熱転写シートの受像層の表面近傍に転写
されるために光の影響を受は易いためと考えられる。However, with the conventional thermal transfer sheet 1-, the transferred image has poor light resistance, the clarity of the transferred image decreases during storage, and a beautiful image cannot be maintained for a long period of time. This is thought to be because in the sublimation transfer method, in which the dye is sublimated and transferred by applying energy in a short period of time using a thermal head, the dye is transferred near the surface of the image-receiving layer of the thermal transfer sheet, so it is easily affected by light. .
本発明者らは上記問題を解決すべく鋭意研究した結果、
スチレン系樹脂または少なくともスチレン系樹脂を含有
する樹脂混合物で受像層を構成した場合、著しく耐光性
を改善し得ることを見出し、本発明を完成するに至った
。As a result of intensive research by the present inventors to solve the above problem,
The present inventors have discovered that light resistance can be significantly improved when the image-receiving layer is composed of a styrene resin or a resin mixture containing at least a styrene resin, and the present invention has been completed.
即ち、本発明は熱転写シートの色材層中の昇華性染料を
加熱転写せしめて画像情報に応じた記録がされる受像層
と、該受像層が担持される基材とを有する被熱転写シー
トにおいて、受像層構成樹脂としてスチレン系樹脂又は
少なくともスチレン系樹脂を含有する樹脂混合物を使用
することを特徴とする被熱転写シートを要旨とするもの
である。That is, the present invention provides a thermal transfer sheet having an image receiving layer in which a sublimable dye in a coloring material layer of a thermal transfer sheet is thermally transferred to record image information in accordance with the image information, and a base material on which the image receiving layer is supported. The gist of the present invention is a thermal transfer sheet characterized in that a styrene resin or a resin mixture containing at least a styrene resin is used as the resin constituting the image receiving layer.
以下、本発明の実施例を図面を参照して説明する。 Embodiments of the present invention will be described below with reference to the drawings.
第1図は本発明の被熱転写シー1−1の一実施態様を示
し、該被熱転写シート1は基材2と、基材2上に設けら
れた受像層3とから構成されている。FIG. 1 shows an embodiment of a thermal transfer sheet 1-1 of the present invention, and the thermal transfer sheet 1 is composed of a base material 2 and an image receiving layer 3 provided on the base material 2.
基材2としてはコート紙、コンデンサーペーパー、グラ
シン紙、硫酸紙、またはサイス度の高い祇あるいはポリ
エステルフィルム等のプラスデックフィルムやミクロボ
イドを有するポリプロビレン主体のいわゆる合成紙等の
如き可撓性のシートまたはフィルノ、が挙げられる。こ
れらのうちコンデンサーペーパー、ポリエチレンテレフ
タレートフィルムが主として用いられ、特に耐熱性を重
視する場合にはコンデンサーペーパーが好ましく、m城
的強度(耐破断性)を重視する場合にはポリエチレンテ
レフタレートフィルムが好ましい。The base material 2 may be a flexible sheet such as coated paper, condenser paper, glassine paper, parchment paper, or a plus deck film such as a polyester film or a polyester film having a high degree of sizing, or a so-called synthetic paper mainly composed of polypropylene having microvoids. Firno is an example. Among these, condenser paper and polyethylene terephthalate film are mainly used. In particular, condenser paper is preferable when heat resistance is important, and polyethylene terephthalate film is preferable when high strength (breakage resistance) is important.
これら基材2の厚さは通常50〜400μrn。The thickness of these base materials 2 is usually 50 to 400 μrn.
特に70〜170μmが好ましい。Particularly preferred is 70 to 170 μm.
本発明においては受像層3はスチレン系樹脂または少な
(ともスチレン系樹脂を含有する樹脂混合物から構成さ
れる。In the present invention, the image receiving layer 3 is composed of a styrene resin or a resin mixture containing a small amount of styrene resin.
上記スチレン系樹脂としては、スチレン系ホモポリマー
、α−メチルスチレンとビニルトルエンとの共重合体、
α−メチルスチレンとスチレンとの共重合体、スチレン
系モノマーとアクリル系モノマーとの共重合体、スチレ
ン系モノマーとアクリロニトリルリとの共重合体、スチ
レン系モノマーと無水マレイン酸との共重合体、スチレ
ン系モノマーとアクリルエステルとアクリルアミドとの
共重合体等が挙げられる。The above-mentioned styrene resin includes a styrene homopolymer, a copolymer of α-methylstyrene and vinyltoluene,
Copolymers of α-methylstyrene and styrene, copolymers of styrene monomers and acrylic monomers, copolymers of styrene monomers and acrylonitrile, copolymers of styrene monomers and maleic anhydride, Examples include copolymers of styrene monomers, acrylic esters, and acrylamide.
上記スチレン系樹脂の具体例の一部を示ずと、ハイマー
SBM−100、ハイマーS B M−73F1ハイマ
−SAM−955(以」ニスチレンーアクリル系、三菱
化成工業■製)、KA1039−8(スチレン−アクリ
ル系、加用化学工業(株製)、RMr)−451,1(
スチレン−アクリロニトリル系、UCC社製)、TYR
IL−767(スチレン−アクリロニトリル系、Dow
社製)、CYMACloo(スチレンーアクリロニI・
リル系、ACC社製)、オキジランク5H−101(ス
チレン−マレイン酸共重合樹脂、日本触媒化学工業■製
)等が挙げられる。Specific examples of the above-mentioned styrene resins include Hymer SBM-100, Hymer SBM-73F1, Hymer SAM-955 (hereinafter referred to as Nistyrene-Acrylic, manufactured by Mitsubishi Chemical Corporation), KA1039-8. (Styrene-acrylic, manufactured by Kanyo Kagaku Kogyo Co., Ltd., RMr) -451,1 (
Styrene-acrylonitrile type, manufactured by UCC), TYR
IL-767 (styrene-acrylonitrile type, Dow
), CYMACloo (styrene-acryloni I・
(Ryl series, manufactured by ACC), and Oxidilanc 5H-101 (styrene-maleic acid copolymer resin, manufactured by Nippon Shokubai Chemical Co., Ltd.).
上記スチレン系樹脂は単独でも或いは二種以上を混合し
て使用することも可能である。The above styrene resins can be used alone or in combination of two or more.
又、本発明においては、上記スチレン系樹脂と他の樹脂
との混合物を受像層構成樹脂として使用することも可能
である。Further, in the present invention, it is also possible to use a mixture of the above styrene resin and other resins as the resin constituting the image receiving layer.
」二記スチレン系樹脂と混合して使用する樹脂として、
例えば、塩化ビニル−酢酸ヒニル共Y1合体、ポリツタ
クリル酸エステル、ポリアクリル酸エステル、セルロー
スアセドブデレー1・等が挙げられる。” As a resin to be used in combination with the styrenic resin listed in Section 2,
Examples include vinyl chloride-hinyl acetate co-Y1 combination, polybutacrylic acid ester, polyacrylic acid ester, cellulose acedobutylene 1.
これらの樹脂の1種或いは2種以」−とスチレン系樹脂
との混合物を使用することができる。スチレン系樹脂と
他の樹脂との混合割合としては、スチレン系樹脂100
重量部に対し、他の樹脂力月00〜900重量部程度で
ある。A mixture of one or more of these resins and a styrene resin can be used. The mixing ratio of styrene resin and other resins is 100% styrene resin.
The amount of other resins is about 00 to 900 parts by weight.
スチレン系樹脂と塩化ビニル−酢酸ビニル共重合体系樹
脂を混合することにより、コーティング適正の改良、膜
の物性改良(可撓性の向上)等の利点がある。塩化ビニ
ル−酢酸ビニル共重合体の具体例としては、VYITH
,VMCH(UCC社製)等があげられる。By mixing a styrene resin and a vinyl chloride-vinyl acetate copolymer resin, there are advantages such as improved coating suitability and improved film properties (improved flexibility). A specific example of vinyl chloride-vinyl acetate copolymer is VYITH
, VMCH (manufactured by UCC), etc.
又、ポリエステル樹脂を混合することにより、染料の染
着性の同士、塗布適正の改良等の利点がある。ポリエス
テル+M脂の具体例としては、vy1on200 (
東洋紡製) 、TP220.TP235 (日本合成製
)等が挙げられる。Further, by mixing polyester resin, there are advantages such as improved dyeability and coating suitability. A specific example of polyester + M resin is vy1on200 (
manufactured by Toyobo), TP220. Examples include TP235 (manufactured by Nippon Gosei).
本発明においては受像層3の白色度を向1−シて転写画
像の鮮明度を更に高めるとともに被熱転写シーI−表面
に筆記性を付与し、かつ転写された画像の再転写を防止
する目的で受像層3中に白色顔料を添加することができ
る。又、白色顔事:Iを添加することにより、より鮮明
度が高く、市・1熱性、耐湿性に優れた画像の転写が行
い得る。In the present invention, the whiteness of the image-receiving layer 3 is improved to further enhance the clarity of the transferred image, and the objective is to provide writability to the surface of the thermally transferred sheet I and to prevent re-transfer of the transferred image. A white pigment can be added to the image-receiving layer 3. Furthermore, by adding White Face I, it is possible to transfer images with higher clarity and excellent heat resistance and humidity resistance.
白色顔料としては、酸化チタン、酸化亜鉛、カオリンク
レー等が用いられ、これらは2種以上混合しても用いる
ことができる。酸化チタンとしてはアナターゼ型酸化チ
タン、ルチル型酸化チタンを用いることができ、アナタ
ーゼ型酸化チタンとしては例えばKA−10、KA、−
1+ 5. KA−20、KA−30,KA−35,
KA−60,KA−80,に’A−90(いずれもチタ
ン工業@増製)、ルチル系酸化チタンとしてはKR−3
1O5KR−380、K R−460、K R−480
(いずれもチタン工業■製)等が挙げられる。白色顔料
の添加量は受像層3を構成する樹脂100重量部に対し
5〜50重量部が好ましい。As the white pigment, titanium oxide, zinc oxide, kaolin clay, etc. are used, and two or more of these can be used as a mixture. As the titanium oxide, anatase type titanium oxide and rutile type titanium oxide can be used, and examples of the anatase type titanium oxide include KA-10, KA, -
1+ 5. KA-20, KA-30, KA-35,
KA-60, KA-80, 'A-90 (all manufactured by Titanium Kogyo@Masusei), KR-3 as rutile titanium oxide
1O5KR-380, K R-460, K R-480
(all manufactured by Titanium Kogyo ■), etc. The amount of the white pigment added is preferably 5 to 50 parts by weight per 100 parts by weight of the resin constituting the image receiving layer 3.
本発明に於いて、上記受像層3中に紫外線吸収剤を添加
することもできる。紫外線吸収剤を添加することにより
、染着した染料の面]光性が更に向上する。紫外線吸収
剤としては、ベンヅフェノン系、ヒンダードアミン系、
ベンゾトリアヅール系等が挙げられる。又、その添加量
は受像層3を構成する樹脂100重量部に対し0.05
〜5重量部程度である。In the present invention, an ultraviolet absorber may also be added to the image receiving layer 3. By adding an ultraviolet absorber, the surface brightness of the dye is further improved. As ultraviolet absorbers, benzphenone type, hindered amine type,
Examples include benzotriadules. The amount added is 0.05 parts by weight per 100 parts by weight of the resin constituting the image receiving layer 3.
~5 parts by weight.
本発明の被熱転写シート1は、熱転写シートとの剥離性
を向−)−4LLめるために受像層3中に離型剤を含有
ゼしめることができろ。離型剤としてはポリエチレンワ
ックス、アミドワックス、テフロンパウダー等の固形ワ
ックス類;弗素系、燐酸エステル系の界面活性剤;シリ
コーンオイル等が挙げられるがシリコーンオイルが好ま
しい。The thermal transfer sheet 1 of the present invention may contain a release agent in the image-receiving layer 3 in order to improve releasability from the thermal transfer sheet. Examples of the mold release agent include solid waxes such as polyethylene wax, amide wax, and Teflon powder; fluorine-based and phosphoric acid ester-based surfactants; and silicone oil, with silicone oil being preferred.
」二記シリコーンオイルとしては油状のものも用いるこ
とができるか、硬化型のものが好ましい。2. As the silicone oil, an oily one can be used, or a hardened type is preferable.
硬化型のシリコーンオイルとしては、反応硬化型、光硬
化型、触媒硬化型等が挙げられるが、反応硬化型のシリ
コーンオイルが特に好ましい。反応硬化型シリコーンオ
イルとして4J、アミン変性シリコーンオイルとエポキ
シ変性シリコーンオイルとを反応硬化させたものが好ま
し、り、アミン変性シリコーンオイルとし、てはKF−
3!’13.Kl嘔−857、KF 858.X
22 3680.X−22−380IC<信越化学工業
@製)等か挙げられ、エポキシ変性シリコーンオイルと
してill、KF−]00T、KF−101,KF−(
io−164、K1−103 (信越化学工業(■q
)笠か挙げられる。また触媒硬化型あるいしょ光硬化型
シリコーンオイルとしてはK S −705F −P
S 、 KS−705F−PS−1,、KS−17(1
−PL−3(以上、触媒硬化型シリコーンオイル、信越
化学工業(+1)製)、KS−720,KS−774−
P■、−3(以上、光硬化型シリコーンオイル、信越化
学工業■製)等が挙げられる。これら硬化型シリ1−ン
オイルの添加量は受像層3を構成する樹脂100重量部
に対し0.5〜30重量部が好ましい。Examples of the curable silicone oil include reaction curable, photocurable, and catalytic curable silicone oils, with reaction curable silicone oils being particularly preferred. The reaction-curing silicone oil is preferably 4J, which is obtained by reaction-curing amine-modified silicone oil and epoxy-modified silicone oil, and amine-modified silicone oil is preferably KF-
3! '13. Kl-857, KF 858. X
22 3680. X-22-380IC<manufactured by Shin-Etsu Chemical Co., Ltd.) etc., and examples of epoxy-modified silicone oils include ill, KF-]00T, KF-101, KF-(
io-164, K1-103 (Shin-Etsu Chemical (■q
) Kasaka is mentioned. In addition, KS-705F-P is a catalyst-curing type or light-curing type silicone oil.
S, KS-705F-PS-1,, KS-17 (1
-PL-3 (catalytic curing silicone oil, manufactured by Shin-Etsu Chemical (+1)), KS-720, KS-774-
Examples include P■, -3 (photocurable silicone oil, manufactured by Shin-Etsu Chemical Co., Ltd.), and the like. The amount of the curable silicone oil added is preferably 0.5 to 30 parts by weight per 100 parts by weight of the resin constituting the image receiving layer 3.
又、第2図に示すように受像層3の表面の一部に、上記
離型剤を適当な溶媒に溶解あるいは分散させて塗布した
後、乾燥させる等によって離型剤層4を設けることもで
きろ。弯11型剤層4を構成する離型剤としては前記し
たアミノ変性シリコノーンオイルとエポキシ変性シリコ
ーンオイルとの反応硬化物が特に好ましい。離型剤層4
の厚さは0゜01〜5μm、特に0.05〜2μmが好
ましい。Alternatively, as shown in FIG. 2, a release agent layer 4 may be provided on a part of the surface of the image-receiving layer 3 by dissolving or dispersing the above-mentioned release agent in a suitable solvent and applying the solution, followed by drying. You can do it. As the mold release agent constituting the curve 11 type agent layer 4, a reaction cured product of the above-mentioned amino-modified silicone oil and epoxy-modified silicone oil is particularly preferred. Mold release agent layer 4
The thickness is preferably 0.01 to 5 μm, particularly 0.05 to 2 μm.
離型剤層4は第2し]に示すように受像層3表面の一部
に設けても、取いは全面に設りても良いが受像@3表面
の一部に設けた場合、離型剤層4の設りられていない部
分にはトノ1−インパクト記録、感熱ン容融転写記録や
鉛筆等による記録を行うことができ、離型剤層・1の設
置3られた部分に昇華転写記録を行い、離型剤層4の設
Jlられていない部分に他の記録方式による記録を行・
う等、昇華転写記録方式とllhの記録方式とをあわせ
て行うことができる。The release agent layer 4 may be provided on a part of the surface of the image-receiving layer 3 as shown in [2], or the release agent layer 4 may be provided on the entire surface of the image-receiving layer 3, but if it is provided on a part of the surface of the image-receiving layer 3, On the part where the molding agent layer 4 is not provided, it is possible to perform recording with a toner 1-impact recording, heat-sensitive melt transfer recording, pencil, etc., and sublimation can be performed on the part where the molding agent layer 1 is installed. Transfer recording is performed, and recording is performed using another recording method on the part of the release agent layer 4 that is not provided.
For example, the sublimation transfer recording method and the llh recording method can be used together.
本発明の被熱転t5:シート1は第3図に示すように基
+12と受像層3との間にクッション層5を設置:lる
ごと力辷でき、クッション層5を設しノるとノイスが少
なく画像情報に対応した画像を再現性良く転写記録する
ことができる。クッション層5を構成する利質としては
例えばウレタン樹脂、アクリル樹脂、エチレン系樹脂、
ブタジェンラバー、エポキシ樹脂等が挙げられる。クッ
ション層5の厚さは2〜20μm程度が好ましい。Heat transfer t5 of the present invention: The sheet 1 has a cushion layer 5 between the base 12 and the image receiving layer 3 as shown in FIG. An image with less noise and corresponding to image information can be transferred and recorded with good reproducibility. Examples of materials constituting the cushion layer 5 include urethane resin, acrylic resin, ethylene resin,
Examples include butadiene rubber and epoxy resin. The thickness of the cushion layer 5 is preferably about 2 to 20 μm.
又、基材の裏面に滑性層を設けることもできる。Moreover, a slippery layer can also be provided on the back surface of the base material.
被熱転写シートは積め重ねて]枚ずつ送り出し7て転写
を行う場合があり、この場合滑性層を設けるとシート同
志の滑りが円滑となり、一枚ず一つ正f1vに送り出ず
ことができる。滑性層の月質としては、メチルメタクリ
レ−1〜等のメククリレ−1・樹脂若しくは対応するア
クリl/−1・樹脂、塩化ビニル−酢酸ビニル共重合体
等のビニル系樹脂等が/トげられる。There are cases where the sheets to be thermally transferred are stacked and fed out one by one for transfer. In this case, providing a slippery layer allows the sheets to slide smoothly against each other, making it possible to avoid sending out one sheet at a time to the correct f1v. . As the lubricant of the slippery layer, meccryle-1 resin such as methyl methacrylate-1 or the corresponding acrylate l/-1 resin, vinyl resin such as vinyl chloride-vinyl acetate copolymer, etc. may be used. can be lost.
又、被熱転写シートに帯電防止剤を含有ゼしめることも
できろ。帯電防止剤を含有せしめろことにより、シート
同志の滑りをより円滑にすることができるとともに、被
熱転写シー1−のほこりの(=J着を防止する効果かあ
る。帯電防止剤は基月或いは受像層r1弓こ含有せしめ
°ζも。Lいし、成し弓31帯電防止剤層として基材裏
面等に設げることができるが、基月裏面に帯電防止層と
して設けることが好ましい。It is also possible to incorporate an antistatic agent into the thermal transfer sheet. By containing an antistatic agent, it is possible to make the sheets slide more smoothly, and it also has the effect of preventing dust from adhering to the thermal transfer sheet 1-. The image-receiving layer r1 contains a cylindrical layer.Although the cylindrical layer 31 can be provided as an antistatic agent layer on the back surface of the base material, it is preferably provided as an antistatic layer on the back surface of the base material.
又、本発明では被熱転写シートに検知マークを設けるこ
とも可能である。検知マークは熱転写シートと被熱転写
シートとの位置決めを行う際等に極めて便利であり、例
えば、光電管検知装置により検知しうる検知マークを基
材裏面等に印刷等により設置ノることができる。Further, in the present invention, it is also possible to provide a detection mark on the thermal transfer sheet. The detection mark is extremely convenient when positioning the thermal transfer sheet and the thermal transfer sheet, and for example, a detection mark that can be detected by a phototube detection device can be placed on the back surface of the substrate by printing or the like.
上記の如き構成を有する本発明の被熱転写シート1は第
4図に示すように熱転写シート6の色材層7と被熱転写
シー1−1の受像層3とが接触するように熱転写シー]
・6と重ね合わせ、熱転写シート6の支持材8側よりサ
ーマルヘット等により加熱した後、転写シート6を剥離
することにより色材層7中の昇華性染$ミ1が被熱転写
シート1の受像層3に転写され、被熱転写シート]に画
像情報に応じた画像が記録される。熱転写シート6に用
いられる昇華性染料としては分子量が約150〜600
程度の比較的低分子量の分散染料、オイル染料、ある種
の塩基性染′1−1、或いはこれらの染ギ、1に変化し
得る中間体が挙げられ、これら昇華性染1パ1は熱転写
温度、熱転写効率、色材、演色性、1li1候性等を考
慮して選択して用いられる。熱転写シート6の色材層7
は」1記昇華性染料を合成樹脂バインダーに分散せしめ
て支持材8表面に塗布する等により形成される。このよ
うな合成樹脂バインダーとしてはエチルセルロース、ヒ
トロキシエヂルセルロース、エチルヒドロキシエチルセ
ルロス、ヒドロキシプロピルセルロース、メチルセルロ
ース、酢酸セルロース、酢醋酸セルロース等のセルTI
−ス系tA4脂;ポリビニルアルコール、ポリビニルブ
チラール、ポリビニルピロリドン、ポリエステル、ポリ
酢酸ヒニル、ポリアクリルアミI・等のビニル系樹脂等
が挙げられる。これらの樹脂の・うちでも耐酸性の優れ
たポリビニルブチラール、あるいはセルロース系樹脂が
好ましい。また熱転写シー1−6の支持材8としてはポ
リエステルフィルム、ポリスチレンフィルム、ポリサル
フォンフィルム、ボリヒニルアルコールフイルム、セロ
ファンフィルム等が挙げられるが、特に耐熱性の点から
ポリエステルフィルムカ呻了ましい。上記支持材8の厚
さは0.5−50μm、竹に3〜10μmが好ましい。The thermal transfer sheet 1 of the present invention having the above-mentioned configuration is arranged such that the color material layer 7 of the thermal transfer sheet 6 and the image receiving layer 3 of the thermal transfer sheet 1-1 are in contact with each other as shown in FIG.
・After heating with a thermal head or the like from the support material 8 side of the thermal transfer sheet 6 and peeling off the transfer sheet 6, the sublimable dye 1 in the color material layer 7 is transferred to the thermal transfer sheet 1. The image is transferred to layer 3, and an image corresponding to the image information is recorded on the thermal transfer sheet. The sublimable dye used in the thermal transfer sheet 6 has a molecular weight of about 150 to 600.
Examples include relatively low molecular weight disperse dyes, oil dyes, certain basic dyes, or intermediates that can be converted into these dyes. They are selected and used in consideration of temperature, thermal transfer efficiency, coloring materials, color rendering properties, weatherability, etc. Color material layer 7 of thermal transfer sheet 6
is formed by dispersing the sublimable dye described in item 1 in a synthetic resin binder and applying it to the surface of the support material 8. Examples of such synthetic resin binders include cell TI such as ethylcellulose, hydroxyethylcellulose, ethylhydroxyethylcellulose, hydroxypropylcellulose, methylcellulose, cellulose acetate, and cellulose acetate.
Examples include vinyl resins such as polyvinyl alcohol, polyvinyl butyral, polyvinylpyrrolidone, polyester, polyhinyl acetate, and polyacrylamide I. Among these resins, polyvinyl butyral or cellulose resin, which has excellent acid resistance, is preferred. The support material 8 of the thermal transfer sheet 1-6 may include polyester film, polystyrene film, polysulfone film, polyhinyl alcohol film, cellophane film, etc., and polyester film is particularly preferred from the viewpoint of heat resistance. The thickness of the support material 8 is preferably 0.5 to 50 μm, preferably 3 to 10 μm for bamboo.
熱転写シート6はサーマルヘッド等の加熱手段により支
持材8側より加熱されるが、支持材8の加熱される面に
ワックス等の滑剤や離型剤を含む滑性層を設けることが
好ましく、サールマヘソド等の加熱手段と支持材8との
融着防止を図ることができる。The thermal transfer sheet 6 is heated from the support material 8 side by heating means such as a thermal head, but it is preferable to provide a lubricating layer containing a lubricant such as wax or a mold release agent on the surface of the support material 8 to be heated. It is possible to prevent the heating means such as the above from being fused to the supporting material 8.
以■に具体的実施例を挙げて本発明を更に詳細に説明す
る。Hereinafter, the present invention will be explained in more detail with reference to specific examples.
実施例1
片面にコロナ放電処理が施された厚さ6μmのポリエヂ
レンテレフタレーi−フィルム(東洋紡製:5−PE′
l’)を支持)Aとし、該支持+Aのコロナ放電処理が
施された面子に丁記組成の色材層組成物をワイ″)・−
バーコーティングにより乾燥時の厚さが]μmとなるよ
うに塗布して色材層を形成し、裏面にシリコ−ンオイル
(X−41−400巨
3 A : 信越シリコーン製)をスポイトにて2滴垂
らした後、全面に広げて滑性層を形成してクリ1転写シ
ートとした。Example 1 Polyethylene terephthalate i-film (manufactured by Toyobo: 5-PE') with a thickness of 6 μm and which was subjected to corona discharge treatment on one side.
l') is set as support) A, and a coloring material layer composition having the composition shown in the table is applied to the corona discharge treated surface of the support +A.
Apply bar coating to a dry thickness of μm to form a coloring layer, and apply 2 drops of silicone oil (X-41-400 Giant 3 A: Shin-Etsu Silicone) on the back side with a dropper. After dripping, it was spread over the entire surface to form a slippery layer to obtain a Clear 1 transfer sheet.
色材層組成物
分散染料 4重量部(日本化
薬製;カヤセフ 1ブルー136)エチルヒドロキシエ
チルセルロース 5重h」部(バーキュレス社製)
トルエン 40重尾部メチルエ
チルヶ]・ン 40重堅部ジオキザン
10重景iN+(一方、150.+
1mの合成紙(玉子油化製: Y [J PO−FPG
−150)を基材とし、ごの表面に1;記組成の受像層
組成物をワイフヤーハー:j−ティングにより乾燥時の
厚さが41zmとなるように塗布してドライヤーで仮乾
燥後、100°Cのオーブン中で30分間乾燥させて受
像層を形成し、被熱転写シートとした。Coloring material layer composition Disperse dye 4 parts by weight (made by Nippon Kayaku; Kayasef 1 Blue 136) Ethyl hydroxyethyl cellulose 5 parts by weight (manufactured by Vercules) Toluene 40 parts by weight methyl ethyl 40 parts by weight Dioxane
10 heavy view iN+ (on the other hand, 150.+
1m synthetic paper (manufactured by Tamago Yuka: Y [J PO-FPG
-150) as a base material, the image-receiving layer composition having the composition shown in step 1 was applied to the surface of the iron using a wire-hardening method to a dry thickness of 41 mm, and after temporary drying with a dryer, it was heated at 100°. The image receiving layer was formed by drying in oven C for 30 minutes, and a thermal transfer sheet was obtained.
受像層組成物
ハイマーSBM100(三菱化成製:スチレン−アクリ
ル系コポリマー) 14重量部KF−393
(信越シリコーン製ニアミノ変性シリコーンオイル)
1重量部X−22−343(信越シ
リコーン製:エポキシ変性シリコーンオイル)
1重量部トルエン 42
重量部メチルエチルケトン 42重量部上
記熱転写シートと被熱転写シートとを色材層と受像層と
が接触するように重ね合わせ、熱転写シートの支持材側
よりサールマヘソドにより、サーマルヘットの出力IW
/ドツト、パルス幅0゜3〜0. 45m/ s e
c、 ドツト密度3 l ノ ト/+uで加熱し、被
熱転写シートの受像層に熱転写シー]・の色材層中のシ
アン色の分散染料を転写ゼしめたところ鮮明にシアン色
の画像が転写された。Image-receiving layer composition Hymer SBM100 (manufactured by Mitsubishi Kasei: styrene-acrylic copolymer) 14 parts by weight KF-393
(Niamino modified silicone oil made by Shin-Etsu Silicone)
1 part by weight X-22-343 (manufactured by Shin-Etsu Silicone: epoxy modified silicone oil)
1 part by weight toluene 42
Parts by weight Methyl ethyl ketone 42 parts by weight The above thermal transfer sheet and the sheet to be thermally transferred are superimposed so that the coloring material layer and the image receiving layer are in contact with each other, and the output IW of the thermal head is applied from the supporting material side of the thermal transfer sheet using a saalmahesod.
/dot, pulse width 0°3~0. 45m/s e
When the cyan disperse dye in the color material layer of the thermal transfer sheet was transferred to the image receiving layer of the thermal transfer sheet by heating at a dot density of 3 l note/+u, a clear cyan image was transferred. It was done.
つぎに被熱転写シートに転写された画像の耐光性試験及
び耐熱耐湿性試験を以下に示す条件で行った。耐光性試
験後の画像の退色率を測定した結果退色率は91%であ
った。又、印字前と百1光性試験、耐熱耐湿性試験後の
被熱転写シートのハンター白色度を測定し比較したとこ
ろ、fl、)印字前、(2)耐光性試験後、(3)耐熱
耐湿性試験後の各々のハンター白色度は、+1.+92
.5、+2+9]、、0、f3) 90 。Next, the image transferred to the thermal transfer sheet was subjected to a light resistance test and a heat resistance and moisture resistance test under the conditions shown below. The fading rate of the image after the light fastness test was measured and the fading rate was 91%. In addition, we measured and compared the Hunter whiteness of the heat transfer sheet before printing and after the 101 light resistance test and heat resistance and humidity resistance test. Each hunter's whiteness after the sex test was +1. +92
.. 5, +2+9], 0, f3) 90.
5であった。It was 5.
耐光性試験
、JIS LO842に基づく条件で10時間暴露し
た。Light resistance test, exposed for 10 hours under conditions based on JIS LO842.
耐熱耐湿性試験 40℃、湿度90%の雰囲気下に100時間保持した。Heat and humidity resistance test It was kept in an atmosphere of 40° C. and 90% humidity for 100 hours.
尚、退色率はMacbeth反射型濃度旧(RIl−9
18)で印字直後の画像濃度と試験後の画像濃度を測定
し、印字直後の画像濃度で試験後の画像濃度を割った百
分率で表す。In addition, the fading rate is based on Macbeth reflective type density old (RIl-9
In step 18), the image density immediately after printing and the image density after the test are measured, and expressed as a percentage of the image density after the test divided by the image density immediately after printing.
更に画像の転写された被熱転写シートの受像層側に乾式
静電複写用上質紙を重ね合わせ、30g/ clの圧力
を加えて60℃のオーブン中に3日間放置した後、オー
ブンより取り出して乾式静電複写用上質紙を被熱転写シ
ートより剥がし乾式静電複写用−1−質紙面に再転写さ
れた画像濃度を前記と同様のMacbeLh濃度計にて
測定して再転写濃度を測定した結果、再転写濃度は0.
28であった。Furthermore, high-quality paper for dry electrostatic copying was placed on the image-receiving layer side of the thermal transfer sheet with the image transferred, and after applying a pressure of 30 g/cl and leaving it in an oven at 60°C for 3 days, it was removed from the oven and dried. The high quality paper for electrostatic copying was peeled off from the thermal transfer sheet, and the image density retransferred to the surface of the high quality paper for dry electrostatic copying was measured using a MacbeLh densitometer similar to the above, and the retransfer density was measured. Retransfer density is 0.
It was 28.
実施例2
実施例1と同様の基材上に下記組成の受像層組成物をワ
イヤーバーコーティングにより乾燥時の厚さが10μm
となるように塗布して乾燥させ、受像層を形成した。Example 2 An image-receiving layer composition having the following composition was coated on the same substrate as in Example 1 with a wire bar to a dry thickness of 10 μm.
An image-receiving layer was formed by coating and drying to form an image-receiving layer.
受像層組成物
ハイマーSBM100(三菱化成製:スチレン−アクリ
ル系コポリマー) 7重量部オキシラック
5T(−101(日本触媒化学工業■製:スチレンーマ
レイン酸ポリマー:融点190〜200℃)
7重量部K1−393 <信越シリコ
ーン製アミノ変性シリコーンオイル)
1重量部X−22343(信越シリコーン製エポ
キシ変性シリコーンオイル) 1重量
部トルエン 42重量部メチル
エチルケトン 42重量部実施例1と同様
の熱転写シートを用いて同様の条件で転写を行ったとこ
ろ、鮮明にシアン色が転写された。Image-receiving layer composition Hymer SBM100 (manufactured by Mitsubishi Kasei: styrene-acrylic copolymer) 7 parts by weight Oxirac 5T (-101 (manufactured by Nippon Shokubai Chemical Co., Ltd.: styrene-maleic acid polymer: melting point 190-200°C)
7 parts by weight K1-393 <amino-modified silicone oil manufactured by Shin-Etsu Silicone)
1 part by weight Color transferred.
次ぎにこの被熱転写シートの耐光性試験を実施例1と同
様の条件で行い、耐光性試験後の退色率を測定した結果
、退色率は86%であった。Next, a light resistance test of this thermal transfer sheet was carried out under the same conditions as in Example 1, and the rate of color fading after the light resistance test was measured. As a result, the rate of color fading was 86%.
実施例3
実施例1と同様の基材上に下記組成の受像層組成物をワ
イヤーバーコーティングにより乾燥時の厚さが4μmと
なるように塗布して乾燥させ被熱転写シートとした。Example 3 An image-receiving layer composition having the following composition was coated on the same substrate as in Example 1 by wire bar coating so that the dry thickness was 4 μm and dried to obtain a thermal transfer sheet.
受像層組成物
ハイマーSBM100(三菱化成製:スチレン−アクリ
ル系コポリマー) 14重量部トルエン
43重量部メチルエチルケトン
43重量部ついで受像層表面の一部に、
下記組成の離型材組成物をワイヤーバーコーティングに
より乾燥時の厚さが0.5μmとなるように塗布して乾
燥さ−け、離型材層を形成して被熱転写シートとした。Image-receiving layer composition Hymer SBM100 (styrene-acrylic copolymer manufactured by Mitsubishi Kasei) 14 parts by weight toluene
43 parts by weight of methyl ethyl ketone 43 parts by weight Then, on a part of the surface of the image-receiving layer,
A mold release material composition having the following composition was coated by wire bar coating so that the dry thickness was 0.5 μm and allowed to dry to form a mold release material layer to obtain a thermal transfer sheet.
離型剤組成
Kl’−393(信越シリコーン製ニアミノ変性シリコ
ーンオイル) 1重量部X−22−
343(信越シリコーン製:エポキシ変性シリコーンオ
イル) 1重量部メタノール
98重置部この被熱転写シートに実施例1と
同様の熱転写シートを用いて同様の条件で転写を行った
とごろ、鮮明にシアン色が転写された。次ぎにこの被熱
転写シートの耐光性試験を実施例Iと同様の条件で行い
、耐光性試験後の退色率を測定した結果、退色率は9]
%であった。Release agent composition Kl'-393 (Niamino modified silicone oil manufactured by Shin-Etsu Silicone) 1 part by weight X-22-
343 (Shin-Etsu Silicone: Epoxy modified silicone oil) 1 part by weight methanol
98 Overlap Portion When the thermal transfer sheet was transferred to this thermal transfer sheet under the same conditions as in Example 1, the cyan color was clearly transferred. Next, a light resistance test of this thermal transfer sheet was conducted under the same conditions as in Example I, and the rate of discoloration after the light resistance test was measured. As a result, the rate of discoloration was 9.
%Met.
実施例4
実施例1と同様の基材上に下記組成の受像層組+11を
’ワイヤーバーコーティングにより乾燥時の厚さが10
μmとなるように塗布して乾燥させ、受像層を形成した
。Example 4 An image-receiving layer set +11 having the following composition was coated on the same base material as in Example 1 by wire bar coating to a dry thickness of 10.
It was coated to a thickness of .mu.m and dried to form an image-receiving layer.
受像層組成物
KALO39−3(加用化学工業@勢製:スチレンアク
リル系コポリマー:Tg=64℃)14重量部
KF−393(信越シリコーン製ニアミノ変性シリコー
ンオイル) 1重量部X−22−3
43(信越シリコーン製=エポキシ変性シリコーンオイ
ル) 1重量部KA−10(チタン工業性
;酸化チタン)2重量部
メチルエチルケトン 41重量部トルエン
41重量部この被熱転写シー
トに実施例1と同様の熱転写シートを用いて同様の条件
で転写を行ったところ、鮮明にシアン色が転写された。Image-receiving layer composition KALO39-3 (manufactured by Kanyo Kagaku Kogyo@Sei: styrene-acrylic copolymer: Tg = 64°C) 14 parts by weight KF-393 (neamino-modified silicone oil manufactured by Shin-Etsu Silicone) 1 part by weight X-22-3
43 (manufactured by Shin-Etsu Silicone = epoxy-modified silicone oil) 1 part by weight KA-10 (titanium industrial grade; titanium oxide) 2 parts by weight Methyl ethyl ketone 41 parts by weight Toluene 41 parts by weight This thermal transfer sheet was coated with the same thermal transfer sheet as in Example 1. When the transfer was performed under the same conditions using the same method, a clear cyan color was transferred.
つぎに被熱転写シートに転写された画像の耐光性試験及
び耐熱耐湿性試験を実施例1と同様の条件で行った。耐
光性試験後の画像の退色率を測定した結果退色率は94
%であった。又、印字前と耐光性試験、耐熱耐湿性試験
後の被熱転写シートのハンター白色度を測定し比較した
ところ、fll印字前、(2)耐光性試験後、(3)耐
熱耐湿性試験後の各々のハンター白色度は、(1)94
.0、(2193,5、f3)93.0であった。Next, a light resistance test and a heat resistance and moisture resistance test of the image transferred to the thermal transfer sheet were conducted under the same conditions as in Example 1. The fading rate of the image after the light fastness test was measured and the fading rate was 94.
%Met. In addition, when we measured and compared the Hunter whiteness of the thermal transfer sheet before printing, after the light resistance test, and after the heat resistance and humidity resistance test, we found that before full printing, (2) after the light resistance test, and (3) after the heat resistance and humidity resistance test. The whiteness of each hunter is (1)94
.. 0, (2193,5, f3) 93.0.
又、実施例1と同様に再転写濃度を測定した結果、再転
写濃度は0.10であった。Further, as a result of measuring the retransfer density in the same manner as in Example 1, the retransfer density was 0.10.
実施例5
実施例1と同様の基材上に下記組成のクッション層を組
成物をワイヤーバーコーティングにより乾燥時の厚さが
10μmとなるように塗布して乾燥させ、クッション層
を形成した。Example 5 A cushion layer having the following composition was coated on the same base material as in Example 1 by wire bar coating so that the dry thickness was 10 μm and dried to form a cushion layer.
クッション層組成物
エルバロイ742(エチレン系樹脂: T g = −
32℃) 15.0重量部トルエ
ン 42.5重量部メチルエチルケ
トン 42.5重量部ついでクッション層の上
に実施例1と同様の受像層組成物をワイヤーバーコーテ
ィングにより乾燥時の厚さが4μmとなるように塗布し
て乾燥させ実施例1と同様の熱転写シートを用いて同様
の条件で転写を行ったところ、鮮明にシアン色が転写さ
れた。Cushion layer composition Elvaloy 742 (ethylene resin: T g = −
32°C) 15.0 parts by weight Toluene 42.5 parts Methyl ethyl ketone 42.5 parts by weight Next, the same image receiving layer composition as in Example 1 was coated on the cushion layer with a wire bar to give a dry thickness of 4 μm. When it was applied and dried and transferred under the same conditions using the same thermal transfer sheet as in Example 1, a clear cyan color was transferred.
次ぎにこの被熱転写シートの耐光性試験を実施例1と同
様の条件で行い、耐光性試験後の退色率を測定した結果
、退色率は91%であった。Next, a light resistance test of this thermal transfer sheet was conducted under the same conditions as in Example 1, and the rate of color fading after the light resistance test was measured. As a result, the rate of color fading was 91%.
実施例6
実施例1と同様の基材上に下記組成の受像層組成物をワ
イヤーバーコーティングにより乾燥時の厚さが10μm
となるように塗布して乾燥させ、受像層を形成した。Example 6 An image-receiving layer composition having the following composition was coated on the same substrate as in Example 1 with a wire bar to a dry thickness of 10 μm.
An image-receiving layer was formed by coating and drying to form an image-receiving layer.
受像層組成物
ヒコテノクスJOO(α−メチルスチレンとビニルトル
エンとの共重合体;バーキュレス社製)15重量部
トルエン 30重量部メチルエ
チルヶI−ン 30重量部シクロへキ号ノ
ン 22重量部KF−393,5重量部
(信越シリコーン製)
X −22−34,35重量部
(信越シリコーン製)
実施例1と同様の熱転写シートを用いて同様の条件で転
写を行ったところ、鮮明にシアン色が転写された。Image-receiving layer composition Hycotenox JOO (copolymer of α-methylstyrene and vinyltoluene; manufactured by Vercules) 15 parts by weight Toluene 30 parts by weight Methyl ethyl chloride 30 parts by weight Cycloquinone 22 parts by weight KF-393, 5 parts by weight (manufactured by Shin-Etsu Silicone) Ta.
実施例7
実施例1と同様の粘材−にに下記組成の受像層組成物を
ワイヤーバーコーティングにより乾燥時の厚さが7μm
となるように塗布して乾燥さゼ、受像層を形成した。Example 7 An image-receiving layer composition having the following composition was applied to the same sticky material as in Example 1 by wire bar coating to a dry thickness of 7 μm.
After coating and drying, an image-receiving layer was formed.
受像層組成物
ハイマーSBM100(三菱化成01製;スヂレンーア
クリル系コポリマー) 10重量部塩化ビニル
−酢酸ビニル共重合体 4重里部(V Y HT−I
:ユニオンカーハイド製)Krl−3931重量部
(信越シリコーン製ニアミノ変性シリニ1−ン)X−2
1−3431重量部
(信越シリコーン製:エポキシ変性シリコーン)メチル
エチルケトン 84重量部実施例1と同様
の熱転写シートを用いて同様の条件で転写を行ったとこ
ろ、鮮明にシアン色が転写された。Image-receiving layer composition Hymer SBM100 (manufactured by Mitsubishi Kasei 01; styrene-acrylic copolymer) 10 parts by weight Vinyl chloride-vinyl acetate copolymer Quadruple parts (V Y HT-I
: manufactured by Union Carhide) Krl-3931 parts by weight (Niamin modified silicone manufactured by Shin-Etsu Silicone) X-2
1-3431 parts by weight (manufactured by Shin-Etsu Silicone: epoxy-modified silicone) Methyl ethyl ketone 84 parts by weight When transfer was performed under the same conditions using the same thermal transfer sheet as in Example 1, a cyan color was clearly transferred.
次ぎにこの被熱転写シー1〜の耐光性試験を実施例1と
同様の条件で行い、耐光性試験後の退色率を測定した結
果、退色率は85%であった。Next, the heat transfer sheet 1~ was subjected to a light resistance test under the same conditions as in Example 1, and the rate of color fading after the light resistance test was measured. As a result, the rate of color fading was 85%.
比較例1
実施例1と同様の基材」二に、スチレン共重合体の代わ
りにVylon200 (東洋紡製ポリエステル:Tg
−67°C)を用い他の組成物含有量は実施例1と同様
の受像層組成物をワイヤーバーコーティングにより乾燥
時の厚さが5μmとなるように塗布して乾燥さセ被熱転
写シートとした。Comparative Example 1 The same base material as in Example 1. Second, Vylon 200 (polyester manufactured by Toyobo Co., Ltd.: Tg
-67°C), and the image-receiving layer composition with the other compositions similar to those in Example 1 was applied by wire bar coating to a dry thickness of 5 μm and dried. did.
この被熱転写シートに実施例1と同様の熱転写シートを
用いて同様の条件で転写を行った。次いでこの被熱転写
シートの耐光性試験を実施例1と同様の条件で行い、耐
光性試験後の退色率を測定した結果、退色率は50%で
あった。Transfer was performed on this thermal transfer sheet using the same thermal transfer sheet as in Example 1 under the same conditions. Next, a light resistance test of this heat transfer sheet was conducted under the same conditions as in Example 1, and the rate of color fading after the light resistance test was measured. As a result, the rate of color fading was 50%.
以上説明したように本発明の被熱転写シートは熱転写シ
ートの色月層中の昇華性染料が転写される受像層をスチ
レン系樹脂又は少なくともスチレン系樹脂を含有する混
合樹脂からなるものとすることより、受像層に転写され
た画像の耐光性が優れ、転写された画像の色彩の低下が
極めて小さく、画像の鮮明度を長期間に亘って転写直後
とほぼ同等に維持することができる等種々の効果を有す
る。As explained above, in the thermal transfer sheet of the present invention, the image receiving layer to which the sublimable dye in the color layer of the thermal transfer sheet is transferred is made of a styrene resin or a mixed resin containing at least a styrene resin. , the image transferred to the image-receiving layer has excellent light resistance, the color of the transferred image is extremely low in color deterioration, and the clarity of the image can be maintained for a long period of time at almost the same level as immediately after transfer. have an effect.
BB
図面の本発明の実施例を示し、第1図は本発明被熱転回
シートの一実施態様を示す縦断面図、第2図は本発明被
熱転写シートの他の実施態様を示す縦断面図、第3図は
更に他の実施態様を示す縦断面図、第4図は熱転写シー
トと被熱転写シートとを重ね合ね−けて被熱転写シート
に熱転写シートの昇華性染料を転写する状態を示す縦断
面図である。
■・・・被熱転写シート
2・・・基材
3・・・受像層Embodiments of the present invention are shown in the drawings, and FIG. 1 is a longitudinal sectional view showing one embodiment of the heat transfer sheet of the present invention, and FIG. 2 is a longitudinal sectional view showing another embodiment of the heat transfer sheet of the present invention. FIG. 3 is a longitudinal sectional view showing still another embodiment, and FIG. 4 is a longitudinal sectional view showing a state in which the thermal transfer sheet and the thermal transfer sheet are not overlapped and the sublimable dye of the thermal transfer sheet is transferred to the thermal transfer sheet. It is a front view. ■...Thermal transfer sheet 2...Base material 3...Image receiving layer
Claims (16)
せしめて画像情報に応じた記録がされる受像層と、該受
像層が担持される基材とを有する被熱転写シートにおい
て、受像層構成樹脂としてスチレン系樹脂又は少なくと
もスチレン系樹脂を含有する樹脂混合物を使用すること
を特徴とする被熱転写シート。(1) A thermal transfer sheet having an image-receiving layer on which a sublimable dye in a coloring material layer of the thermal transfer sheet is heated and recorded in accordance with image information, and a base material on which the image-receiving layer is supported. A thermal transfer sheet characterized in that a styrene-based resin or a resin mixture containing at least a styrene-based resin is used as a layer-constituting resin.
特許請求の範囲第1項記載の被熱転写シート。(2) The thermal transfer sheet according to claim 1, wherein the resin constituting the image-receiving layer is a styrene homopolymer.
ルエンとの共重合体である特許請求の範囲第1項記載の
被熱転写シート。(3) The thermal transfer sheet according to claim 1, wherein the resin constituting the image receiving layer is a copolymer of α-methylstyrene and vinyltoluene.
との共重合体である特許請求の範囲第1項記載の被熱転
写シート。(4) The thermal transfer sheet according to claim 1, wherein the resin constituting the image receiving layer is a copolymer of α-methylstyrene and styrene.
系モノマーとの共重合体である特許請求の範囲第1項記
載の被熱転写シート。(5) The thermal transfer sheet according to claim 1, wherein the resin constituting the image receiving layer is a copolymer of a styrene monomer and an acrylic monomer.
ニトリルとの共重合体である特許請求の範囲第1項記載
の被熱転写シート。(6) The thermal transfer sheet according to claim 1, wherein the resin constituting the image receiving layer is a copolymer of a styrene monomer and acrylonitrile.
イン酸との共重合体である特許請求の範囲第1項記載の
被熱転写シート。(7) The thermal transfer sheet according to claim 1, wherein the resin constituting the image receiving layer is a copolymer of a styrene monomer and maleic anhydride.
エステルとアクリルアミドとの共重合体である特許請求
の範囲第1項記載の被熱転写シート。(8) The thermal transfer sheet according to claim 1, wherein the resin constituting the image receiving layer is a copolymer of a styrene monomer, acrylic ester, and acrylamide.
−メチルスチレンとビニルトルエンとの共重合体、α−
メチルスチレンとスチレンとの共重合体、スチレン系モ
ノマーとアクリル系モノマーとの共重合体、スチレン系
モノマーとアクリルニトリルとの共重合体、スチレン系
モノマーと無水マレイン酸との共重合体、スチレン系モ
ノマーとアクリルエステルとアクリルアミドとの共重合
体のうち少なくとも2種以上の混合樹脂を使用する特許
請求の範囲第1項記載の被熱転写シート。(9) The resin constituting the image receiving layer is a styrene homopolymer, α
-Copolymer of methylstyrene and vinyltoluene, α-
Copolymers of methylstyrene and styrene, copolymers of styrene monomers and acrylic monomers, copolymers of styrene monomers and acrylonitrile, copolymers of styrene monomers and maleic anhydride, styrene-based The thermal transfer sheet according to claim 1, which uses a mixed resin of at least two types of copolymers of monomers, acrylic esters, and acrylamide.
重合体、ポリメタクリル酸エステル、ポリアクリル酸エ
ステル、セルロースアセトブチレートの群から選ばれた
少なくとも1種類の樹脂とスチレン系樹脂との混合物で
ある特許請求の範囲第1項記載の被熱転写シート。(10) The resin constituting the image-receiving layer is a mixture of at least one resin selected from the group of vinyl chloride-vinyl acetate copolymer, polymethacrylate, polyacrylate, and cellulose acetobutyrate and styrene resin. A thermal transfer sheet according to claim 1.
とエポキシ変性シリコーンとの反応物を含有する特許請
求の範囲第1項〜第10項のいずれかに記載の被熱転写
シート。(11) The thermal transfer sheet according to any one of claims 1 to 10, wherein the image-receiving layer contains a reaction product of amino-modified silicone and epoxy-modified silicone as a release agent.
てなる特許請求の範囲第1項〜第11項のいずれかに記
載の被熱転写シート。(12) The thermal transfer sheet according to any one of claims 1 to 11, wherein a release agent layer is provided on a part or the entire surface of the image-receiving layer.
性シリコーンとを反応せしめてなる特許請求の範囲第1
2項記載の被熱転写シート。(13) Claim 1 in which the mold release agent layer is formed by reacting amino-modified silicone and epoxy-modified silicone.
The thermal transfer sheet according to item 2.
請求の範囲第12項記載の被熱転写シート。(14) The thermal transfer sheet according to claim 12, wherein the release agent layer is made of catalyst-curing silicone.
レーよりなる群から選ばれた1種または2種以上を、樹
脂100重量部に対し5〜20重量部含有せしめてなる
特許請求の範囲第1項〜第14項のいずれかに記載の被
熱転写シート。(15) The image-receiving layer contains 5 to 20 parts by weight of one or more selected from the group consisting of titanium oxide, zinc oxide, and kaolin clay based on 100 parts by weight of the resin. The thermal transfer sheet according to any one of items 1 to 14.
る特許請求の範囲第1項〜第15項のいずれかに記載の
被熱転写シート。(16) The thermal transfer sheet according to any one of claims 1 to 15, wherein a cushion layer is provided between the image-receiving layer and the base material.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23828885 | 1985-10-24 | ||
JP60-238288 | 1985-10-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62189195A true JPS62189195A (en) | 1987-08-18 |
JP2622675B2 JP2622675B2 (en) | 1997-06-18 |
Family
ID=17027960
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61042846A Expired - Lifetime JP2622675B2 (en) | 1985-10-24 | 1986-02-28 | Heat transfer sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2622675B2 (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01228889A (en) * | 1988-03-09 | 1989-09-12 | Dainippon Printing Co Ltd | Heat transfer image bearing sheet |
JPH01229692A (en) * | 1988-03-11 | 1989-09-13 | Dainippon Printing Co Ltd | Thermal transfer receiving sheet |
JPH01229689A (en) * | 1988-03-11 | 1989-09-13 | Dainippon Printing Co Ltd | Thermal transfer receiving sheet |
JPH01229695A (en) * | 1988-03-11 | 1989-09-13 | Dainippon Printing Co Ltd | Thermal transfer receiving sheet |
JPH01229691A (en) * | 1988-03-11 | 1989-09-13 | Dainippon Printing Co Ltd | Thermal transfer receiving sheet |
JPH01237195A (en) * | 1988-03-18 | 1989-09-21 | Dainippon Printing Co Ltd | Receiving sheet for thermal transfer |
JPH01237194A (en) * | 1988-03-18 | 1989-09-21 | Dainippon Printing Co Ltd | Receiving sheet for thermal transfer |
JPH01238986A (en) * | 1988-03-18 | 1989-09-25 | Dainippon Printing Co Ltd | Receiving sheet for thermal transfer |
JPH02151488A (en) * | 1988-12-02 | 1990-06-11 | Konica Corp | Thermal recording material |
WO1990008659A1 (en) * | 1989-01-30 | 1990-08-09 | Dai Nippon Insatsu Kabushiki Kaisha | Image reception sheet |
US5268348A (en) * | 1989-01-30 | 1993-12-07 | Dai Nippon Insatsu Kabushiki Kaisha | Image-receiving sheet |
JP2009190384A (en) * | 2008-02-18 | 2009-08-27 | Dainippon Printing Co Ltd | Heat transfer image receiving sheet |
JP2010076399A (en) * | 2008-09-29 | 2010-04-08 | Dainippon Printing Co Ltd | Heat transfer image receiving sheet |
JP2010149342A (en) * | 2008-12-24 | 2010-07-08 | Fujikura Kasei Co Ltd | Resin composition for dye acceptable layer |
EP2287008A2 (en) | 2009-08-18 | 2011-02-23 | Sony Corporation | Resin composition, thermal transfer-receiving sheet, and method for making thermal transfer-receiving sheet |
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JPS5985792A (en) * | 1982-11-10 | 1984-05-17 | Matsushita Electric Ind Co Ltd | Image-receiving body for thermal transfer recording |
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JPS59165688A (en) * | 1983-03-11 | 1984-09-18 | Shin Nisso Kako Co Ltd | Thermal transfer recording material |
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JPS60112484A (en) * | 1983-11-24 | 1985-06-18 | Matsushita Electric Ind Co Ltd | Image-receiving material |
JPS6219488A (en) * | 1985-07-19 | 1987-01-28 | Canon Inc | Heat-sensitive transfer recording media and heat-sensitive transfer recording method |
JPS6221580A (en) * | 1985-07-22 | 1987-01-29 | Sony Corp | Printing paper for sublimation transfer type hard copying |
JPS6244495A (en) * | 1985-08-23 | 1987-02-26 | Mitsubishi Rayon Co Ltd | Coating composition for recording body of sublimable thermal transfer recording system |
JPS6246688A (en) * | 1985-08-26 | 1987-02-28 | Mitsubishi Rayon Co Ltd | Recording material for sublimation-type thermal transfer recording system |
JPS6246689A (en) * | 1985-08-27 | 1987-02-28 | Mitsubishi Rayon Co Ltd | Coating composition for producing recording material for sublimation-type thermal transfer recording system |
JPS6248596A (en) * | 1985-08-28 | 1987-03-03 | Mitsubishi Rayon Co Ltd | Recording material for use in sublimation-type thermal transfer recording system |
JPS6250193A (en) * | 1985-08-30 | 1987-03-04 | Mitsubishi Rayon Co Ltd | Recording material of sublimation type thermal transfer recording system |
JPS6250188A (en) * | 1985-08-29 | 1987-03-04 | Mitsubishi Rayon Co Ltd | Coating compound for recording material of sublimation-type thermal transfer recording system |
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JPS5985792A (en) * | 1982-11-10 | 1984-05-17 | Matsushita Electric Ind Co Ltd | Image-receiving body for thermal transfer recording |
JPS59150796A (en) * | 1983-02-18 | 1984-08-29 | Mitsubishi Electric Corp | Transfer-type thermal recording method |
JPS59165688A (en) * | 1983-03-11 | 1984-09-18 | Shin Nisso Kako Co Ltd | Thermal transfer recording material |
JPS59214696A (en) * | 1983-05-20 | 1984-12-04 | Ricoh Co Ltd | Thermal transfer accepting sheet |
JPS6025793A (en) * | 1983-07-25 | 1985-02-08 | Dainippon Printing Co Ltd | Sheet for heat transfer printing |
JPS6082393A (en) * | 1983-10-13 | 1985-05-10 | Nec Corp | Recording paper and its preparation |
JPS60112484A (en) * | 1983-11-24 | 1985-06-18 | Matsushita Electric Ind Co Ltd | Image-receiving material |
JPS6034898A (en) * | 1984-07-17 | 1985-02-22 | Dainippon Printing Co Ltd | Thermal transfer recording sheet |
JPS6219488A (en) * | 1985-07-19 | 1987-01-28 | Canon Inc | Heat-sensitive transfer recording media and heat-sensitive transfer recording method |
JPS6221580A (en) * | 1985-07-22 | 1987-01-29 | Sony Corp | Printing paper for sublimation transfer type hard copying |
JPS6244495A (en) * | 1985-08-23 | 1987-02-26 | Mitsubishi Rayon Co Ltd | Coating composition for recording body of sublimable thermal transfer recording system |
JPS6246688A (en) * | 1985-08-26 | 1987-02-28 | Mitsubishi Rayon Co Ltd | Recording material for sublimation-type thermal transfer recording system |
JPS6246689A (en) * | 1985-08-27 | 1987-02-28 | Mitsubishi Rayon Co Ltd | Coating composition for producing recording material for sublimation-type thermal transfer recording system |
JPS6248596A (en) * | 1985-08-28 | 1987-03-03 | Mitsubishi Rayon Co Ltd | Recording material for use in sublimation-type thermal transfer recording system |
JPS6250188A (en) * | 1985-08-29 | 1987-03-04 | Mitsubishi Rayon Co Ltd | Coating compound for recording material of sublimation-type thermal transfer recording system |
JPS6250193A (en) * | 1985-08-30 | 1987-03-04 | Mitsubishi Rayon Co Ltd | Recording material of sublimation type thermal transfer recording system |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01228889A (en) * | 1988-03-09 | 1989-09-12 | Dainippon Printing Co Ltd | Heat transfer image bearing sheet |
JPH01229692A (en) * | 1988-03-11 | 1989-09-13 | Dainippon Printing Co Ltd | Thermal transfer receiving sheet |
JPH01229689A (en) * | 1988-03-11 | 1989-09-13 | Dainippon Printing Co Ltd | Thermal transfer receiving sheet |
JPH01229695A (en) * | 1988-03-11 | 1989-09-13 | Dainippon Printing Co Ltd | Thermal transfer receiving sheet |
JPH01229691A (en) * | 1988-03-11 | 1989-09-13 | Dainippon Printing Co Ltd | Thermal transfer receiving sheet |
JPH01237195A (en) * | 1988-03-18 | 1989-09-21 | Dainippon Printing Co Ltd | Receiving sheet for thermal transfer |
JPH01237194A (en) * | 1988-03-18 | 1989-09-21 | Dainippon Printing Co Ltd | Receiving sheet for thermal transfer |
JPH01238986A (en) * | 1988-03-18 | 1989-09-25 | Dainippon Printing Co Ltd | Receiving sheet for thermal transfer |
JPH02151488A (en) * | 1988-12-02 | 1990-06-11 | Konica Corp | Thermal recording material |
WO1990008659A1 (en) * | 1989-01-30 | 1990-08-09 | Dai Nippon Insatsu Kabushiki Kaisha | Image reception sheet |
US5135905A (en) * | 1989-01-30 | 1992-08-04 | Dai Nippon Insatsu Kabushiki Kaisha | Image-receiving sheet |
US5268348A (en) * | 1989-01-30 | 1993-12-07 | Dai Nippon Insatsu Kabushiki Kaisha | Image-receiving sheet |
JP2009190384A (en) * | 2008-02-18 | 2009-08-27 | Dainippon Printing Co Ltd | Heat transfer image receiving sheet |
JP2010076399A (en) * | 2008-09-29 | 2010-04-08 | Dainippon Printing Co Ltd | Heat transfer image receiving sheet |
JP2010149342A (en) * | 2008-12-24 | 2010-07-08 | Fujikura Kasei Co Ltd | Resin composition for dye acceptable layer |
EP2287008A2 (en) | 2009-08-18 | 2011-02-23 | Sony Corporation | Resin composition, thermal transfer-receiving sheet, and method for making thermal transfer-receiving sheet |
US8545949B2 (en) | 2009-08-18 | 2013-10-01 | Sony Corporation | Resin composition, thermal transfer-receiving sheet, and method for making thermal transfer-receiving sheet |
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Legal Events
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EXPY | Cancellation because of completion of term |