JPH0345391A - Thermal transfer cover film - Google Patents
Thermal transfer cover filmInfo
- Publication number
- JPH0345391A JPH0345391A JP1180471A JP18047189A JPH0345391A JP H0345391 A JPH0345391 A JP H0345391A JP 1180471 A JP1180471 A JP 1180471A JP 18047189 A JP18047189 A JP 18047189A JP H0345391 A JPH0345391 A JP H0345391A
- Authority
- JP
- Japan
- Prior art keywords
- ionizing radiation
- thermal transfer
- layer
- resin layer
- cured resin
- 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
- 239000013039 cover film Substances 0.000 title claims description 26
- 229920005989 resin Polymers 0.000 claims abstract description 55
- 239000011347 resin Substances 0.000 claims abstract description 55
- 239000010408 film Substances 0.000 claims description 40
- 239000002245 particle Substances 0.000 claims description 7
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 12
- 230000005865 ionizing radiation Effects 0.000 abstract description 11
- 238000005299 abrasion Methods 0.000 abstract description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 8
- 238000010894 electron beam technology Methods 0.000 abstract description 7
- 239000000178 monomer Substances 0.000 abstract description 6
- 229920000178 Acrylic resin Polymers 0.000 abstract description 5
- 239000004925 Acrylic resin Substances 0.000 abstract description 5
- 239000003822 epoxy resin Substances 0.000 abstract description 3
- 229920000647 polyepoxide Polymers 0.000 abstract description 3
- 229920000728 polyester Polymers 0.000 abstract description 3
- 239000004721 Polyphenylene oxide Substances 0.000 abstract description 2
- 239000003999 initiator Substances 0.000 abstract description 2
- 229920000570 polyether Polymers 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 62
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000001993 wax Substances 0.000 description 16
- 238000000034 method Methods 0.000 description 14
- 238000000859 sublimation Methods 0.000 description 11
- 230000008022 sublimation Effects 0.000 description 11
- 239000000975 dye Substances 0.000 description 10
- 239000011241 protective layer Substances 0.000 description 7
- -1 polypropylene Polymers 0.000 description 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 5
- 238000001723 curing Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000012790 adhesive layer Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- 229920001225 polyester resin Polymers 0.000 description 4
- 239000004645 polyester resin Substances 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000986 disperse dye Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000001815 facial effect Effects 0.000 description 3
- 238000007756 gravure coating Methods 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent 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
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- ZVPQQKPBYFAWKR-UHFFFAOYSA-N C[C]CC Chemical compound C[C]CC ZVPQQKPBYFAWKR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 238000001227 electron beam curing Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
Landscapes
- Electronic Switches (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Supply, Installation And Extraction Of Printed Sheets Or Plates (AREA)
- Accessory Devices And Overall Control Thereof (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は熱転写カバーフィルムに関し、更に詳しくは熱
転写画像等に優れた耐摩擦性等の耐久性を与え、更に熱
転写画像に優れた発色性や光沢を与えることが出来る熱
転写カバーフィルムに関する。Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a thermal transfer cover film, and more specifically, it provides thermal transfer images with excellent durability such as abrasion resistance, and furthermore, provides thermal transfer images with excellent color development and This invention relates to a thermal transfer cover film that can provide gloss.
(従来の技術及びその問題点)
従来、簡便な印刷方法として熱転写方法が広く使用され
る様になった。これらの熱転写方法では、各種の画像が
簡便に形成されるので、印刷枚数が比較的少なくてもよ
い印刷物、例えば、身分証明書等のIDカードの作成等
に利用される様になっている。(Prior Art and its Problems) Conventionally, thermal transfer methods have come to be widely used as a simple printing method. These thermal transfer methods allow various types of images to be easily formed, and are therefore being used to produce printed matter that requires a relatively small number of prints, for example, for the production of ID cards such as identification cards.
又、顔写真等の如くカラー画像が好ましい場合には、連
続した基材フィルム上に、例えば、イエロー、マゼンダ
及びシアン(更に必要に応じてブラック)の着色熱転写
層を面順次に繰返し多数設けた長尺熱転写フィルムを用
いる熱転写方法が行なわれている。If a color image is preferred, such as a photograph of a face, a large number of colored thermal transfer layers of, for example, yellow, magenta, and cyan (and black if necessary) are repeatedly provided in sequence on a continuous base film. A thermal transfer method using a long thermal transfer film has been used.
この様な熱転写フィルムは大別すると、それらの熱転写
層が加熱によって軟化して画像状に被転写材に熱転写さ
れる、所謂ワックスタイプの熱転写フィルムと、加熱に
よって熱転写層中の染料が昇華(熱移行)して染料のみ
が画像状に被転写材上に熱転写する、所謂昇華タイプの
熱転写フィルムとに大別される。These thermal transfer films can be roughly divided into wax-type thermal transfer films, in which the thermal transfer layer softens when heated and is thermally transferred to the transfer material in the form of an image, and wax-type thermal transfer films, in which the dye in the thermal transfer layer is sublimated (heat-transferred) by heating. It is broadly classified into so-called sublimation type thermal transfer film, in which only the dye is thermally transferred in the form of an image onto the transfer material.
以上の如き熱転写フィルムで、身分証明書等のIDカー
ドを作成する場合、ワックスタイプの熱転写フィルムの
場合は、文字や数字等の如き画像の形成は容易であるが
、これらの画像は耐久性、特に耐摩擦性が劣るという欠
点がある。When creating ID cards such as identification cards using the above thermal transfer film, it is easy to form images such as letters and numbers with wax type thermal transfer film, but these images have durability and In particular, it has the disadvantage of poor abrasion resistance.
一方、昇華転写型の熱転写フィルムの場合には、顔写真
等の階調性画像を形成することが出来るが、形成された
画像は通常の印刷インキとは異なり、ビヒクルが無い為
、画像の光沢が不足し、又、同様の理由で耐摩擦性等の
耐久性に劣るという問題がある。On the other hand, in the case of sublimation transfer type thermal transfer film, it is possible to form gradation images such as facial photographs, but unlike normal printing ink, the formed image does not have a vehicle, so the image has a glossy appearance. Furthermore, for the same reason, there is a problem that durability such as abrasion resistance is poor.
この様な問題点を解決する方法としては、形成された画
像面に透明フィルムをラミネートする方法が行われてい
るが、この方法は操作が煩雑であると共に、カード全体
にラミネートする為、カードにカールが生じたり、更に
ラミネートの操作上あまり薄いフィルムは使用出来ず、
従ってカード全体が厚くなるという問題がある。A method to solve these problems is to laminate a transparent film on the formed image surface, but this method is complicated to operate, and since the entire card is laminated, Curling may occur, and it is not possible to use very thin films due to laminating operations.
Therefore, there is a problem that the entire card becomes thick.
又、上記ラミネート方法に代えて、画像面に熱硬化性樹
脂塗料や電離放射線硬化性樹脂塗料を塗布及び硬化させ
る方法もあるが、これらの方法は煩雑であるばかりでな
く、塗料中の溶剤が画像を侵し、又、熱硬化性樹脂を用
いた場合は、硬化時の熱が染料画像を変褐色させる恐れ
がある。In addition, instead of the above laminating method, there is a method of applying and curing a thermosetting resin paint or an ionizing radiation-curable resin paint on the image surface, but these methods are not only complicated, but also cause the solvent in the paint to If a thermosetting resin is used, the heat during curing may cause the dye image to turn brown.
従って、本発明の目的は、」1記従来技術の問題点を解
決し、簡便な操作で耐久性、特に耐摩耗性、光沢、発色
性等に優れ且つカールを生じない優れた画像が形成出来
る熱転写カバーフィルムを提供することである。Therefore, the purpose of the present invention is to solve the problems of the prior art mentioned in 1., and to form an excellent image with excellent durability, especially abrasion resistance, gloss, color development, etc., and without curling, with a simple operation. An object of the present invention is to provide a thermal transfer cover film.
(問題点を解決する為の手段) 上記目的は以下の本発明によって達成される。(Means for solving problems) The above objects are achieved by the present invention as described below.
即ち、本発明は、基材フィルム上に、電離放射線硬化樹
脂層を剥離可能に設けてなることを特徴とする熱転写カ
バーフィルムである。That is, the present invention is a thermal transfer cover film characterized in that an ionizing radiation-cured resin layer is releasably provided on a base film.
(作 用)
基材フィルム上に電離放射線硬化樹脂層を剥離可能に設
け、この電離放射線硬化樹脂層を転写画像の表面に転写
することによって、簡便な操作で耐久性、特に耐摩擦性
、光沢、発色性等に優れ且つカールを生じない優れた画
像が形成出来る。(Function) By providing a peelable ionizing radiation-cured resin layer on the base film and transferring this ionizing radiation-cured resin layer to the surface of the transferred image, durability, especially abrasion resistance, and gloss can be improved with a simple operation. , it is possible to form an image with excellent color development and no curling.
特に好ましい実施態様では電離放射線硬化樹脂層に、比
較的多量の透明性粒子を含有させることによって、転写
時の膜切れが良好となるので、非常に耐摩擦性に優れた
保護層が容易に転写出来る。In a particularly preferred embodiment, the ionizing radiation-curable resin layer contains a relatively large amount of transparent particles, so that the film can be easily cut during transfer, so that a protective layer with excellent abrasion resistance can be easily transferred. I can do it.
(好ましい実施態様)
次に好ましい実施例を図解的に示す添付図面を参照して
本発明を更に具体的に説明する。(Preferred Embodiments) The present invention will now be described in more detail with reference to the accompanying drawings that schematically show preferred embodiments.
第1図は本発明の好ましいl実施例の熱転写カバーフィ
ルムの断面を図解的に示す図であり、この実施例の熱転
写カバーフィルムは、基材フィルム1上に電離放射線硬
化樹脂層2が剥離可能に設けられている。FIG. 1 is a diagram schematically showing a cross section of a thermal transfer cover film according to a preferred embodiment of the present invention. It is set in.
尚、図中の3は剥離層であり、電離放射線硬化樹脂層と
基材フィルムとの接着性を低くして電離放射線硬化樹脂
層の転写を容易にする作用を有する。この層3は基材フ
ィルム1と電離放射線硬化樹脂層との剥離性が優れてい
る場合は不要である。又、4は背面層であり、プリンタ
ーのサーマルヘッドの粘着を防止する作用を有している
。この層4も基材フィルムの耐熱性やスリップ性が良好
である場合には不要である。In addition, 3 in the figure is a peeling layer, which has the effect of lowering the adhesiveness between the ionizing radiation-cured resin layer and the base film to facilitate the transfer of the ionizing radiation-cured resin layer. This layer 3 is unnecessary if the peelability between the base film 1 and the ionizing radiation-cured resin layer is excellent. Further, 4 is a back layer, which has the function of preventing the thermal head of the printer from sticking. This layer 4 is also unnecessary if the base film has good heat resistance and slip properties.
次に使用材料及び形成方法等により本発明の熱転写カバ
ーフィルムを更に詳しく説明する。Next, the thermal transfer cover film of the present invention will be explained in more detail using the materials used, the forming method, etc.
本発明で用いられる基材フィルム1としては、従来の熱
転写フィルムに使用されていると同じ基材フィルムがそ
のまま用いることが出来ると共に、その他のものも使用
することが出来、特に制限されない。As the base film 1 used in the present invention, the same base film used in conventional thermal transfer films can be used as is, and other films can also be used, and there are no particular limitations.
好ましい基材フィルムlの具体例としては、例えば、グ
ラシン紙、コンデンサ紙、パラフィン紙等の薄葉紙が有
用であり、その他に、例えば、ポリエステル、ポリプロ
ピレン、セロハン、ポリカーボネート、酢酸セルロース
、ポリエチレン、ポリ塩化ビニル、ポリスチレン、ナイ
ロン、ボリイミド、ポリ塩化ビニリデン、アイオノマー
等のプラスチック或いはこれらと前核紙とを複合した基
材フィルム等が挙げられる。Specific examples of preferable base films 1 include thin papers such as glassine paper, capacitor paper, and paraffin paper.Other examples include polyester, polypropylene, cellophane, polycarbonate, cellulose acetate, polyethylene, and polyvinyl chloride. Examples include plastics such as polystyrene, nylon, polyimide, polyvinylidene chloride, and ionomer, and base films made of composites of these and procore paper.
この基材フィルム1の厚さは、その強度及び耐熱性等が
適切になる様に、材料に応じて適宜変更することが出来
るが、その厚さは、好ましくは、3乃至100μmであ
る。The thickness of this base film 1 can be changed as appropriate depending on the material so that its strength, heat resistance, etc. are appropriate, but the thickness is preferably 3 to 100 μm.
本発明における電離放射線硬化樹脂層2は、電離放射線
硬化性樹脂から形成する。該硬化性樹脂は、その構造中
にラジカル重合性の二重結合を有するポリマー又はオリ
ゴマー、例えば、比較的低分子量のポリエステル、ポリ
エーテル、アクリル樹脂、エポキシ樹脂、ウレタン樹脂
等の(メタ)アクリレートとラジカル重合性のモノマー
や多官能モノマー等を含有し、更に必要に応じて光重合
開始剤を含有し、電子線や紫外線によって重合架橋する
ものであり、従来公知の電離放射線硬化性樹脂はいずれ
も本発明で使用することが出来、特に限定されない。The ionizing radiation-curable resin layer 2 in the present invention is formed from an ionizing radiation-curable resin. The curable resin is a polymer or oligomer having a radically polymerizable double bond in its structure, such as a (meth)acrylate such as a relatively low molecular weight polyester, polyether, acrylic resin, epoxy resin, or urethane resin. It contains radically polymerizable monomers, polyfunctional monomers, etc., and if necessary, a photopolymerization initiator, and is polymerized and crosslinked by electron beams or ultraviolet rays. It can be used in the present invention and is not particularly limited.
ラジカル重合性のモノマーとしては、例えば、(メタ)
アクリル酸エステル、(メタ)アクリルアミド、アリル
化合物、ビニルエーテル類、ビニルエステル類、ビニル
異部環化合物、N−ビニル化合物、スチレン、(メタ)
アクリル酸、クロトン酸、イタコン酸等が挙げられ、又
、多官能性モノマーとしては、例えば、ジエチレングリ
コールジ(メタ)アクリレ−]・、トリエチレングリコ
ルジ(メタ)アクリレート、テトラエチレングリコール
ジ(メタ)アクリレート、トリメチロールプロパントリ
(メタ)アクリレ−1〜、ペンタエリスリトールテトラ
(メタ)アクリレート、ジペンタエリスリトールへキザ
(メタ)アクリレート、l・リス(β−(メタ)アクリ
ロイロキシエチル)インシアヌレート等が挙げられる。Examples of radically polymerizable monomers include (meth)
Acrylic esters, (meth)acrylamides, allyl compounds, vinyl ethers, vinyl esters, vinyl heterocyclic compounds, N-vinyl compounds, styrene, (meth)
Examples of polyfunctional monomers include diethylene glycol di(meth)acrylate], triethylene glycol di(meth)acrylate, and tetraethylene glycol di(meth)acrylate. Acrylate, trimethylolpropane tri(meth)acrylate-1~, pentaerythritol tetra(meth)acrylate, dipentaerythritol hexa(meth)acrylate, l.lis(β-(meth)acryloyloxyethyl)in cyanurate, etc. can be mentioned.
本発明では上記成分からなる電離放射線硬化性樹脂を、
必要であれば、適当な溶剤や非反応性の透明性樹脂等を
加えて、粘度等を調整してインキを作成し、これを前記
基材フィルムに、例えば、グラビアコート、グラビアリ
バースコート、ロルコートその他多くの手段で塗布、乾
燥及び硬化することによって、電離放射線硬化樹脂層2
を形成する。これらの硬化樹脂層の厚みは0.5乃至2
0um程度の範囲が好ましい。In the present invention, the ionizing radiation curable resin consisting of the above components is
If necessary, add an appropriate solvent or non-reactive transparent resin to adjust the viscosity, etc. to create an ink, and apply this to the base film, for example, by gravure coating, gravure reverse coating, roll coating. By applying, drying and curing by many other means, the ionizing radiation cured resin layer 2
form. The thickness of these cured resin layers is 0.5 to 2
A range of about 0 um is preferable.
電離放射線硬化性樹脂層の硬化には、紫外線又は電子線
等の放射線が使用される。放射線照射には従来技術がそ
のまま使用出来、例えば、電子線硬化の場合にはコツク
ロフトワルトン型、バンプグラフ型、共振変圧型、絶縁
コア変圧器型、直線型、エレクトロカーテン型、ダイナ
ミドロン型、高周波型等の各fm電子線加速機から放出
される50乃至1,0OOKev、好ましくは100乃
至300 KeVのエネルギーを有する電子線等が使用
され、紫外線硬化の場合には超高圧水銀灯、高圧水銀灯
、低圧水銀灯、カーボンアーク、キセノンアーク、メタ
ルハライドランプ等の光源から発する紫外線等が利用さ
れる。勿論、電離放射線による硬化は、硬化性樹脂層の
形成直後であってもよいし、又、全ての層の形成後であ
ってもよい。Radiation such as ultraviolet rays or electron beams is used to cure the ionizing radiation-curable resin layer. Conventional techniques can be used as is for radiation irradiation, for example, in the case of electron beam curing, Kotscroft-Walton type, bump graph type, resonant transformer type, insulated core transformer type, linear type, electrocurtain type, dynamidron type, etc. An electron beam or the like having an energy of 50 to 1,0 OOKev, preferably 100 to 300 KeV, emitted from each fm electron beam accelerator such as a high frequency type is used. Ultraviolet rays emitted from light sources such as low-pressure mercury lamps, carbon arcs, xenon arcs, and metal halide lamps are used. Of course, the curing by ionizing radiation may be performed immediately after the formation of the curable resin layer or after the formation of all the layers.
」1記電離放射線硬化樹脂層の形成に際しては、該硬化
樹脂層に、比較的多量の透明性の高い粒子を添加するの
が好ましい。これらの粒子としては、サブミクロン乃至
数LLmの微粒子のシリカ、アルミナ、炭酸カルシウム
、クルク、クレー等の無機粒子や、アクリル樹脂、ポリ
エステル樹脂、メラミン樹脂、エポキシ樹脂等の有機粒
子が挙げられる。この様な透明性の高い粒子は前記電離
放射線硬化性樹脂100重量部当り10乃至200重量
部の範囲の量で使用することが好ましく、使用量が少な
ずぎると、転写時の膜切れが不十分となり、一方、多す
ぎると保護層としての透明性が不足する様になるので好
ましくない。更に他の添加剤、例えば、ワックス、滑剤
、紫外線吸収剤、酸化防止剤及び/又は蛍光増白剤等の
添加剤を含有させることによって、被覆される各種画像
の滑性、光沢、耐光性、耐候性、白色度等を向上させる
ことが出来る。1. When forming the ionizing radiation-cured resin layer, it is preferable to add a relatively large amount of highly transparent particles to the cured resin layer. These particles include inorganic particles such as silica, alumina, calcium carbonate, curcum, clay, etc., which are submicron to several LLm in size, and organic particles such as acrylic resin, polyester resin, melamine resin, and epoxy resin. It is preferable to use such highly transparent particles in an amount ranging from 10 to 200 parts by weight per 100 parts by weight of the ionizing radiation curable resin. If the amount used is too small, film breakage during transfer may be insufficient. On the other hand, if the amount is too high, the transparency as a protective layer will be insufficient, which is not preferable. Furthermore, by including other additives such as waxes, lubricants, ultraviolet absorbers, antioxidants, and/or optical brighteners, the smoothness, gloss, light fastness, etc. of various images to be coated can be improved. Weather resistance, whiteness, etc. can be improved.
上記電離放射線硬化樹脂層の形成に先立って、基材フィ
ルムの面に剥離層3を形成することが好ましい。かかる
剥&if層はワックス類、シリコーンワックス、シリコ
ーン樹脂、弗素樹脂、アクリル樹脂等の剥離剤から形成
する。形成方法は硬化を除き前記電離放射線硬化樹脂層
の形成方法と同様でよく、その厚みは0.5乃至5μm
程度で十分である。又、転写後に艶消し保護層が望まし
い場合には、剥離層中に各種の粒子を包含させるか或は
剥離層側表面をマット処理した基材フィルムを使用する
ことにより表面マット状にすることも出来る。It is preferable to form a release layer 3 on the surface of the base film prior to forming the ionizing radiation-cured resin layer. The peel & if layer is formed from a release agent such as wax, silicone wax, silicone resin, fluororesin, acrylic resin, or the like. The formation method may be the same as the formation method of the ionizing radiation-cured resin layer except for curing, and the thickness thereof is 0.5 to 5 μm.
It is enough. In addition, if a matte protective layer is desired after transfer, the surface can be made matte by incorporating various particles into the release layer or by using a base film whose surface on the release layer side is matt-treated. I can do it.
更に上記の電離放射線硬化樹脂層の表面には、これらの
層の転写性を良好にする為に、感熱接着剤層5を設ける
ことも出来る。これらの感熱接着剤層は、例えば、アク
リル樹脂、塩化ビニル樹脂、塩化ビニル・酢酸ビニル共
重合樹脂、ポリエステル樹脂等の如く熱時接着性の良好
な樹脂の溶液を塗布及び乾燥することによって、好まし
くは0.5乃至10μm程度の厚みに形成する。Furthermore, a heat-sensitive adhesive layer 5 may be provided on the surface of the above-mentioned ionizing radiation-cured resin layer in order to improve the transferability of these layers. These heat-sensitive adhesive layers are preferably formed by applying and drying a solution of a resin having good adhesive properties when heated, such as acrylic resin, vinyl chloride resin, vinyl chloride/vinyl acetate copolymer resin, polyester resin, etc. is formed to have a thickness of approximately 0.5 to 10 μm.
以上が本発明の熱転写カバーフィルムの構成であるが、
かかるカバーフィルムの電離放射線硬化樹脂層は、基材
フィルム上に単独に設けてもよいし、昇華型染料層やワ
ックスインキ層と面順次に設けてもよいのは当然である
。The above is the structure of the thermal transfer cover film of the present invention,
It goes without saying that the ionizing radiation-curable resin layer of such a cover film may be provided singly on the base film, or may be provided surface-sequentially with the sublimation dye layer or the wax ink layer.
上記の如き熱転写カバーフィルムを用いて保護する画像
は、昇華型熱転写方法及び/又はワックス型熱転写方法
による画像が好ましいが、これらの画像に限定されない
。特に昇華転写画像に適用する場合には、該画像の保護
層が形成されると共に、転写時の熱によって画像を形成
している染料が再発色処理されるので、画像が一層鮮明
になるという効果がある。The image to be protected using the thermal transfer cover film as described above is preferably an image formed by a sublimation type thermal transfer method and/or a wax type thermal transfer method, but is not limited to these images. In particular, when applied to sublimation transfer images, a protective layer is formed for the image, and the dye forming the image is recolored by the heat during transfer, making the image even clearer. There is.
又、昇華転写画像及び/又はワックスタイプ転写画像は
、いずれの被転写材上に形成されたものでもよいが、本
発明において好ましいのは、ポリエステル樹脂や塩化ビ
ニル樹脂等からなるカード基材に形成された画像である
。勿論、これらのカード基材には、エンボス、サイン、
ICメモリー、磁気層、他の印刷等が設けられていても
よいし、カバーフィルム転写後にエンボス、サイン、磁
気層等を設けることも可能である。Further, the sublimation transfer image and/or the wax type transfer image may be formed on any transfer material, but in the present invention, it is preferable to form the sublimation transfer image and/or the wax type transfer image on a card base material made of polyester resin, vinyl chloride resin, etc. This is the image that was created. Of course, these card base materials include embossing, signatures,
An IC memory, a magnetic layer, other printing, etc. may be provided, and it is also possible to provide an embossing, a signature, a magnetic layer, etc. after the cover film is transferred.
上記本発明の熱転写カバーフィルムを用いるカードの製
造例を第2図を参照して説明する。An example of manufacturing a card using the thermal transfer cover film of the present invention will be described with reference to FIG. 2.
先ず、カード基材6の表面に、昇華型熱転写シートのイ
エロー染料層を重ね、色分解信号に従って作動するサー
マルプリンターによりイエロー画像7Yを転写する。同
様に同一領域にマゼンタ画像7M及びシアン画像7Cを
転写して所望のカラー画像7を形成する。次にワックス
インキ型熱転写シートを用いて同様に所望の文字、記号
等8を印字する。更に本発明の熱転写カバーフィルムを
用いて上記カラー画像7及び/又は文字等の画像8上に
電離放射線硬化樹脂層を転写して保護層2を形成する。First, a yellow dye layer of a sublimation type thermal transfer sheet is superimposed on the surface of the card base material 6, and a yellow image 7Y is transferred by a thermal printer operating according to color separation signals. Similarly, a magenta image 7M and a cyan image 7C are transferred to the same area to form a desired color image 7. Next, desired characters, symbols, etc. 8 are similarly printed using a wax ink type thermal transfer sheet. Furthermore, the protective layer 2 is formed by transferring an ionizing radiation-cured resin layer onto the color image 7 and/or images 8 such as characters using the thermal transfer cover film of the present invention.
この様にして所望のカードが得られる。In this way, a desired card can be obtained.
上記の転写に際しては、サーマルプリンターは、昇華転
写用、ワックスインキ転写用、熱転写カバーフィルム用
と別々に(好ましくは連続して)設定してもよいし、又
、これらの転写は、共通のプリンターで夫々印字エネル
ギーを適切に調整して行ってもよい。尚、本発明では加
熱手段としてサーマルプリンターに限定されず、その地
熱板、熱ロール、アイロン等でもよいのは当然である。For the above transfer, the thermal printer may be set separately (preferably consecutively) for sublimation transfer, wax ink transfer, and thermal transfer cover film, or these transfers may be performed using a common printer. The printing energy may be appropriately adjusted in each case. Incidentally, in the present invention, the heating means is not limited to a thermal printer, but it goes without saying that a geothermal plate, a hot roll, an iron, etc. may also be used.
(効 果)
以上の如き本発明によれば、基材フィルム上に電離放射
線硬化樹脂層を剥離可能に設け、この電離放射線硬化樹
脂層を転写画像の表面に転写することによって、簡便な
操作で耐久性、特に耐摩擦性、光沢、発色性等に優れ且
つカールを生じない優れた画像が形成出来る。(Effects) According to the present invention as described above, an ionizing radiation-cured resin layer is removably provided on a base film, and this ionizing radiation-cured resin layer is transferred to the surface of a transferred image, thereby allowing easy operation. It is possible to form an image that has excellent durability, particularly abrasion resistance, gloss, color development, etc., and does not cause curling.
特に好ましい実施態様では電離放射線硬化樹脂層に、比
較的多量の透明性粒子を含有させることによって、転写
時の膜切れが良好となるので、非常に耐摩擦性に優れた
保護層が容易に転写出来る。In a particularly preferred embodiment, the ionizing radiation-curable resin layer contains a relatively large amount of transparent particles, so that the film can be easily cut during transfer, so that a protective layer with excellent abrasion resistance can be easily transferred. I can do it.
(実施例)
次に参考例、実施例、使用例及び比較例を挙げて本発明
を更に具体的に説明する。尚、文中、部又は%とあるの
は特に断りのない限り重量基準である。(Example) Next, the present invention will be described in more detail by giving reference examples, examples, usage examples, and comparative examples. In the text, parts or percentages are based on weight unless otherwise specified.
参考例1 下記組成の3色の昇華性染料を含むインキを調製した。Reference example 1 An ink containing sublimable dyes of three colors having the following composition was prepared.
イエローインキ
分散染料(Macrol、ex、 Yellow 6G
、バイエル社製) 5.
5部ポリビニルブチラール樹脂(エスレックBX−1゜
積木化学製) 4.5部メチルエ
チルケトン/]・ルエン(重量比1/1)89.0部
マゼンタインキ
染料としてマゼンタ分散染料(Disperse Re
d60)を使用した他はイエローインキと同様。Yellow ink disperse dye (Macrol, ex, Yellow 6G
, manufactured by Bayer) 5.
5 parts Polyvinyl butyral resin (S-LEC BX-1゜Made by Tsukiki Kagaku) 4.5 parts Methyl ethyl ketone/]・Luene (weight ratio 1/1) 89.0 parts Magenta ink Magenta disperse dye (Disperse Re)
Same as yellow ink except that d60) was used.
シアンインキ
染料としてシアン分散染料(Solvent Blue
63]を使用した他はイエローインキと同様。Cyan disperse dye (Solvent Blue) is used as cyan ink dye.
Same as yellow ink except that 63] was used.
上記インキ組成物をグラビアコート方法により、背面に
耐熱スリップ層(厚み1μm)を形成し、且つ表面にポ
リウレタン系樹脂からなるプライマー層(厚み0.5μ
m)を形成しである厚さ6.0μmのポリニスデルフィ
ルム(商品名「ルミラー」東しく用製)の表面に、塗布
量が約3g/ポになる様に、夫々イエロー、マゼンタ及
びシアンの順に面順次に幅15cmに繰返し塗布及び乾
燥して3色の昇華性染料層を形成し、昇華型熱転写シー
トを作成した。A heat-resistant slip layer (thickness 1 μm) was formed on the back surface using the above ink composition by gravure coating, and a primer layer (thickness 0.5 μm thick) made of polyurethane resin was formed on the surface.
Yellow, magenta and cyan were applied to the surface of a 6.0 μm thick polynisdel film (trade name "Lumirror" manufactured by Toshiba Co., Ltd.) to form 2. A sublimation type thermal transfer sheet was prepared by repeatedly applying and drying the dye layer in a width of 15 cm in order to form three color sublimable dye layers.
参考例2
下記ワックスインキ組成物を温度100℃で加熱し、ホ
ットメルトによるロールコート法にて、参考例1と同一
の基材フィルムであって、プライマー層の無いフィルム
に、塗布量が約4g/rn’になる様に塗布してワック
スタイプの熱転写シー!・を作成した。Reference Example 2 The following wax ink composition was heated at a temperature of 100°C and coated in an amount of about 4 g on the same base film as Reference Example 1, but without a primer layer, using a hot melt roll coating method. /rn' wax type heat transfer sheet! ·It was created.
ワックスインキ
エステルワックス 1G部酸化ワッ
クス 1G部パラフィンワックス
60部カーボンブラック
12部実施例工
参考例2と同一の基材フィルムに下記組成のインキを用
いて、固形分基準でIg/m’の割合でグラビアコート
方法により塗布及び乾燥して剥離層■
を形成した。Wax ink ester wax 1G part oxidized wax 1G part paraffin wax 60 parts carbon black
12 Parts Example Work An ink having the following composition was coated on the same base film as in Reference Example 2 at a ratio of Ig/m' based on solid content by a gravure coating method and dried to form a release layer (2).
剥離層用インキ
シリコーン系1Δ4脂 10部塩化ビ
ニル/酢酸ビニル共重合体 10部メチルエチルケト
ン 100部トルエン
100部次に上記剥離層の表面に下記インキを固
形分基準でLog/rn”の割合で塗工及び乾燥して電
離放射線硬化性樹脂層を形成した。Ink for release layer Silicone 1Δ4 resin 10 parts Vinyl chloride/vinyl acetate copolymer 10 parts Methyl ethyl ketone 100 parts Toluene
100 parts Next, the following ink was coated on the surface of the release layer at a ratio of Log/rn'' based on solid content and dried to form an ionizing radiation curable resin layer.
電離放 綿 化 層用インキ
ジペンタエリスリト−ルヘキザアクリレート40部
疎水性コロイグルシリ力 40部ポリメチ
ルメタクリレート 20部ポリエチレンワッ
クス 3部メチルエチルヶl−ン
250部トルエン
250部次に上記樹脂層の表面に、下記組成のイン
キを固形分基準でIg/rn’の割合で塗工及び乾燥し
て接着剤層を形成後、日新ハイボルテージ社製電子線照
射装置を用いて窒素1O−7Torrの雰囲気中で、1
80KV及び線量5 M r a dで電子線を間射し
、電離放射線硬化性樹脂層を硬化させ、本発明の熱転写
カバーフィルムを作成した。Ionizing discharge cotton layer ink Dipentaerythritol hexaacrylate 40 parts Hydrophobic colloidal silica 40 parts Polymethyl methacrylate 20 parts Polyethylene wax 3 parts Methyl ethyl carbon
250 parts toluene
250 parts Next, on the surface of the resin layer, an ink having the following composition is applied at a ratio of Ig/rn' based on solid content and dried to form an adhesive layer, and then an electron beam irradiation device manufactured by Nissin High Voltage Co., Ltd. in a nitrogen atmosphere of 10-7 Torr using
The ionizing radiation-curable resin layer was cured by irradiating an electron beam at 80 KV and a dose of 5 M r a d to produce a thermal transfer cover film of the present invention.
浚箆剋置里乙乞ま
塩化ビニル/酢酸ビニル共重合体 10部メチルエチ
ルケトン 100部トルエン
100部実施例2
実施例1における電離放射線硬化性樹脂インキに代えて
、下記インキを使用し、他は実施例1と同様にして本発
明の熱転写カバーフィルムを作成した。Vinyl chloride/vinyl acetate copolymer 10 parts Methyl ethyl ketone 100 parts Toluene
100 copies Example 2 A thermal transfer cover film of the present invention was prepared in the same manner as in Example 1 except that the following ink was used in place of the ionizing radiation-curable resin ink in Example 1.
電離放 硬 樹 層用インキ
トリメチロールプロパントリアクリレート60部
タルク(日本クルク製、ミクロエースL−1)10部
ポリメチルメタクリレ−1・ 30部弗素系
界面活性剤(住友3M製、フローラード432)
3部メチルエチルケトン
200部トルエン
200部使用例】
安定剤等の添加剤を約10%含有するポリ塩化ビニル(
重合度800)コンパウンド100部、白色顔料(酸化
ヂタン)10部及び可塑剤(D。Ionizing discharge ink for hardwood layers 60 parts of trimethylolpropane triacrylate 10 parts of talc (manufactured by Nippon Kuruku, Micro Ace L-1) 1/30 parts of polymethyl methacrylate (manufactured by Sumitomo 3M, Florard 432) )
3-part methyl ethyl ketone
200 parts toluene
Example of using 200 parts] Polyvinyl chloride containing about 10% of additives such as stabilizers (
100 parts of a compound (degree of polymerization: 800), 10 parts of a white pigment (ditane oxide), and a plasticizer (D).
P)0.5部からなるカード基材の面に、参考例1の昇
華型熱転写フィルムの昇華性染料層を重ね、顔写真を色
分解して得た電気信号に連結したサーマルヘッドで熱エ
ネルギーを付与してフルカラー顔写真像を形成し、次に
参考例2のワックスタイプの熱転写フィルムを用いて文
字及び記号を転写形成し、更に上記実施例1の本発明の
熱転写カバーフィルムを用いて各画像部分に転写性保護
層を転写させ、顔写真と各種必要情報を有するカードを
得た。P) A sublimable dye layer of the sublimation type thermal transfer film of Reference Example 1 is overlaid on the surface of a card base material consisting of 0.5 parts, and heat energy is applied using a thermal head connected to electrical signals obtained by color-separating facial photographs. was applied to form a full-color photographic image of the face, then letters and symbols were transferred and formed using the wax-type thermal transfer film of Reference Example 2, and furthermore, each image was formed using the thermal transfer cover film of the present invention of Example 1. A transferable protective layer was transferred to the image area to obtain a card with a facial photograph and various necessary information.
使用例2
実施例2の熱転写カバーフィルムを用い、他は使用例1
ど同様にしてカードを作成した。Usage Example 2 The thermal transfer cover film of Example 2 was used, and the others were the same as Usage Example 1.
I created a card in the same way.
比較例1
使用例1において電離放射線硬化樹脂層を転写させなか
った以夕iが使用例1と同様にしてカードを作成した。Comparative Example 1 A card was prepared in the same manner as in Use Example 1 except that the ionizing radiation-cured resin layer was not transferred in Use Example 1.
比較例2
実施例1における電離放射線硬化樹脂層用インキに代え
て、下記インキを使用した以外は実施例1と同様にして
カバーフィルムを作成し、使用例1と同様にしてカード
を作成した。Comparative Example 2 A cover film was prepared in the same manner as in Example 1, except that the following ink was used instead of the ink for the ionizing radiation-curable resin layer in Example 1, and a card was prepared in the same manner as in Use Example 1.
栄進置里工之ま
ポリエステル樹脂(U−18、荒用化学製)20部メチ
ルエチルケトン 50部トルエン
50部比較例3
実施例1における電離放射線硬化樹脂層用インキに代え
て、下記インキを使用した以外は実施例1と同様にして
カバーフィルムを作成し、使用例1と同様にしてカード
を作成した。Eishin Okisato Kounoma Polyester Resin (U-18, manufactured by Arayo Kagaku) 20 parts Methyl ethyl ketone 50 parts Toluene
50 copies Comparative Example 3 A cover film was created in the same manner as in Example 1, except that the following ink was used instead of the ink for the ionizing radiation-cured resin layer in Example 1, and a card was created in the same manner as in Use Example 1. did.
榮護亘里乙2ま
セルロース樹脂(CAB381−0.1) 2
0部 0
メチルエチルケトン 50部トルエン
50部評価例
以上で得られたカードを評価して下記第1表の結果を得
た。Cellulose resin (CAB381-0.1) 2
0 parts 0 methyl ethyl ketone 50 parts toluene
The cards obtained in 50 copies or more were evaluated and the results shown in Table 1 below were obtained.
膜切れ:転写後のフィルムの剥離性及び転写画像の顕微
鏡観察。Film breakage: Peelability of the film after transfer and microscopic observation of the transferred image.
0:剥離が非常に容易で、電離放射線硬化樹脂層が画像
部りにシャープに切れて
いる。0: Peeling is very easy, and the ionizing radiation-cured resin layer is sharply cut in the image area.
×:剥離に抵抗があり、樹脂層のエツジが乱れている。×: There is resistance to peeling, and the edges of the resin layer are disordered.
耐摩擦性;画像表面をイソプロピルアルコールを含浸さ
せたガーゼで100回擦る。Abrasion resistance: The image surface is rubbed 100 times with gauze impregnated with isopropyl alcohol.
0:ガーゼの汚染なし。0: No contamination of gauze.
○:ガーゼがやや汚染される。○: Gauze is slightly contaminated.
×:ガーゼの汚染大。×: Severe contamination of gauze.
光 沢ニゲロス値%。Hikari Sawa Nigelos value%.
第1図は本発明の熱転写カバーフィルムの断面を図解的
に説明する図であり、第2図は上記カバーフィルムを用
いて作成したカードの断面を図解的に説明する図である
。
1:基材フィルム
2:電離放射線硬化樹脂層
3:剥離層 4:背面層
5:接着層 6:カード基祠7:カラー画像
8:文字等FIG. 1 is a diagram illustrating a cross-section of a thermal transfer cover film of the present invention, and FIG. 2 is a diagram illustrating a cross-section of a card made using the above-mentioned cover film. 1: Base film 2: Ionizing radiation curing resin layer 3: Peeling layer 4: Back layer 5: Adhesive layer 6: Card base 7: Color image 8: Characters, etc.
Claims (4)
可能に設けてなることを特徴とする熱転写カバーフィル
ム。(1) A thermal transfer cover film characterized by having an ionizing radiation-cured resin layer releasably provided on a base film.
離層が設けられている請求項1に記載の熱転写カバーフ
ィルム。(2) The thermal transfer cover film according to claim 1, wherein a release layer is provided between the base film and the ionizing radiation-cured resin layer.
を含有している請求項1に記載の熱転写カバーフィルム
。(3) The thermal transfer cover film according to claim 1, wherein the ionizing radiation-cured resin layer contains a relatively large amount of transparent particles.
線吸収剤、酸化防止剤及び/又は蛍光増白剤が含有され
ている請求項1に記載の熱転写カバーフィルム。(4) The thermal transfer cover film according to claim 1, wherein the ionizing radiation-curable resin layer contains a wax, a lubricant, an ultraviolet absorber, an antioxidant, and/or a fluorescent brightener.
Priority Applications (16)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1180471A JPH0345391A (en) | 1989-07-14 | 1989-07-14 | Thermal transfer cover film |
JP1241929A JP2967538B2 (en) | 1989-07-14 | 1989-09-20 | Thermal transfer sheet and card manufacturing method |
DE69016438T DE69016438T2 (en) | 1989-07-14 | 1990-07-13 | COVER FILM FOR HEAT TRANSFER. |
ES90910943T ES2070327T3 (en) | 1989-07-14 | 1990-07-13 | THERMOTRANSFER COATING FILM. |
DK90910943T DK0487727T3 (en) | 1989-07-14 | 1990-07-13 | For heat treatment transferable cover film |
EP94111077A EP0625429B1 (en) | 1989-07-14 | 1990-07-13 | Heat transfer sheet |
EP19900910943 EP0487727B1 (en) | 1989-07-14 | 1990-07-13 | Thermal transfer cover film |
PCT/JP1990/000909 WO1991001223A1 (en) | 1989-07-14 | 1990-07-13 | Thermal transfer cover film |
DE69032843T DE69032843T2 (en) | 1989-07-14 | 1990-07-13 | Thermal transfer layer |
US08/022,865 US5427997A (en) | 1989-07-14 | 1993-03-01 | Heat transfer cover films |
US08/396,791 US5527759A (en) | 1989-07-14 | 1995-03-01 | Heat transfer cover films |
US08/451,971 US5646089A (en) | 1989-07-14 | 1995-05-26 | Heat transfer cover films |
US08/588,705 US5728645A (en) | 1989-07-14 | 1996-01-19 | Heat transfer cover films |
US09/437,279 US6291062B1 (en) | 1989-07-14 | 1997-12-02 | Heat transfer cover films |
US09/885,094 US6946423B2 (en) | 1989-07-14 | 2001-06-21 | Heat transfer cover films |
US10/635,675 US6786993B2 (en) | 1989-07-14 | 2003-08-07 | Heat transfer cover films |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1180471A JPH0345391A (en) | 1989-07-14 | 1989-07-14 | Thermal transfer cover film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0345391A true JPH0345391A (en) | 1991-02-26 |
Family
ID=16083799
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1180471A Pending JPH0345391A (en) | 1989-07-14 | 1989-07-14 | Thermal transfer cover film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0345391A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001270218A (en) * | 2000-02-04 | 2001-10-02 | Eastman Kodak Co | Transfer laminate element |
KR100456770B1 (en) * | 2001-12-18 | 2004-11-10 | 현대자동차주식회사 | Bite for tip grinding of welding gun |
US6870421B2 (en) | 2002-03-15 | 2005-03-22 | Seiko Epson Corporation | Temperature characteristic compensation apparatus |
JP2007253533A (en) * | 2006-03-24 | 2007-10-04 | Fujifilm Corp | Method for forming image using thermal transfer method and printed matter |
WO2016152918A1 (en) * | 2015-03-23 | 2016-09-29 | 大日本印刷株式会社 | Transfer foil |
US10493730B2 (en) | 2015-03-23 | 2019-12-03 | Dai Nippon Printing Co., Ltd. | Transfer film |
-
1989
- 1989-07-14 JP JP1180471A patent/JPH0345391A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001270218A (en) * | 2000-02-04 | 2001-10-02 | Eastman Kodak Co | Transfer laminate element |
KR100456770B1 (en) * | 2001-12-18 | 2004-11-10 | 현대자동차주식회사 | Bite for tip grinding of welding gun |
US6870421B2 (en) | 2002-03-15 | 2005-03-22 | Seiko Epson Corporation | Temperature characteristic compensation apparatus |
JP2007253533A (en) * | 2006-03-24 | 2007-10-04 | Fujifilm Corp | Method for forming image using thermal transfer method and printed matter |
WO2016152918A1 (en) * | 2015-03-23 | 2016-09-29 | 大日本印刷株式会社 | Transfer foil |
US10493730B2 (en) | 2015-03-23 | 2019-12-03 | Dai Nippon Printing Co., Ltd. | Transfer film |
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