JPH0355550A - Production of colored image forming material - Google Patents
Production of colored image forming materialInfo
- Publication number
- JPH0355550A JPH0355550A JP19166489A JP19166489A JPH0355550A JP H0355550 A JPH0355550 A JP H0355550A JP 19166489 A JP19166489 A JP 19166489A JP 19166489 A JP19166489 A JP 19166489A JP H0355550 A JPH0355550 A JP H0355550A
- Authority
- JP
- Japan
- Prior art keywords
- photosensitive layer
- sheet
- colored photosensitive
- colored
- layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims abstract description 32
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 238000000576 coating method Methods 0.000 claims abstract description 17
- 239000011248 coating agent Substances 0.000 claims abstract description 15
- 238000001035 drying Methods 0.000 claims abstract description 12
- 238000004804 winding Methods 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims description 9
- 239000003086 colorant Substances 0.000 claims description 6
- -1 polypropylene Polymers 0.000 abstract description 18
- 230000000903 blocking effect Effects 0.000 abstract description 7
- 239000004698 Polyethylene Substances 0.000 abstract description 6
- 229920000573 polyethylene Polymers 0.000 abstract description 6
- 239000004743 Polypropylene Substances 0.000 abstract description 4
- 229920001155 polypropylene Polymers 0.000 abstract description 4
- 239000002131 composite material Substances 0.000 abstract description 3
- 229920006362 Teflon® Polymers 0.000 abstract description 2
- 229920003023 plastic Polymers 0.000 abstract description 2
- 239000004033 plastic Substances 0.000 abstract description 2
- 230000003449 preventive effect Effects 0.000 abstract description 2
- 238000010186 staining Methods 0.000 abstract 2
- 239000002985 plastic film Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 description 6
- 239000005020 polyethylene terephthalate Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 235000012730 carminic acid Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000007756 gravure coating Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000007763 reverse roll coating Methods 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 2
- RBKHNGHPZZZJCI-UHFFFAOYSA-N (4-aminophenyl)-phenylmethanone Chemical compound C1=CC(N)=CC=C1C(=O)C1=CC=CC=C1 RBKHNGHPZZZJCI-UHFFFAOYSA-N 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
- HTQNYBBTZSBWKL-UHFFFAOYSA-N 2,3,4-trihydroxbenzophenone Chemical compound OC1=C(O)C(O)=CC=C1C(=O)C1=CC=CC=C1 HTQNYBBTZSBWKL-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 101100309761 Aedes aegypti SDR-1 gene Proteins 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 102100038434 Neuroplastin Human genes 0.000 description 1
- 108700038050 Neuroplastin Proteins 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- ZLSMCQSGRWNEGX-UHFFFAOYSA-N bis(4-aminophenyl)methanone Chemical compound C1=CC(N)=CC=C1C(=O)C1=CC=C(N)C=C1 ZLSMCQSGRWNEGX-UHFFFAOYSA-N 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000003738 black carbon Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- 238000007607 die coating method Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- KKZJGLLVHKMTCM-UHFFFAOYSA-N mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 description 1
- 229960001156 mitoxantrone Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- ICWPRFNZEBFLPT-UHFFFAOYSA-N n-(2-hydroxyphenyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NC1=CC=CC=C1O ICWPRFNZEBFLPT-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride 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
- 238000003825 pressing Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、カラー印刷における色校正用のカラープルー
フに用いる着色画像形成材料に関し、詳しくは画像部分
のみを転写することにより、本印刷時の画像品質により
近似した転写画像を得ることができる着色画像形成材料
の製造方法に関する。Detailed Description of the Invention <Industrial Application Field> The present invention relates to a colored image forming material used for color proofing for color proofing in color printing. The present invention relates to a method for producing a colored image forming material that can obtain a transferred image that is more similar in image quality.
〈従来の技術〉
多色刷印刷における本印刷の前工程として行なわれる校
正刷りの手間と時間の節約に色校正用のカラーシ一ト(
カラープルーフとも呼ばれる〉が用いられるのは当分野
においてよく知られている。<Conventional technology> Color sheets for color proofing (
It is well known in the art that color proofs are used.
色校正用のカラーシ一トを用いて多色転写画像を作或す
る方法としては、例えば特開昭47−41830号公報
に記載の、着色画像を直接最終受像紙に転写積層する直
接転写方式、特開昭59−97140号公報に記載の、
着色画像を一時、仮の受像シート上に転写する、間接転
写方式、また、特開昭56−501217号公報に記載
の、着色感光層を受像紙に転写した後に画像を形成する
工程をくり返す方法等が挙げられる.
これらの方式はいずれも画像を形成した被転写材料表面
が有機重合体層で被覆されているため、得られた画像表
面の光沢が高過ぎ、本印刷時の画像品質とは異なった印
象を与えるという問題を有していたゆ
そこで、この問題を解決するために被転写材料上に着色
画像のみを転写積層し、多色画像を形成する画像のみ転
写方式が考えられた。この方式は、被転写材料上に有機
重合体層で被覆されることがないので、原理的にきわめ
て本印刷時の画像品質に近似した画像を得ることが出来
る.
く発明が解決しようとする課題〉
しかしながら、画像のみを転写法に用いられる着色画像
シートは、加熱ラミネート処理時に、画像のみを熱軟化
層から被転写シートに容易に転写させるために、着色感
光層と熱軟化層との接着性を下げる(剥離性を上げる)
必要がある。そこで、該熱軟化層上に着色感光層を塗布
、乾燥した後、通常のように、着色感光層塗設シ一トを
巻き取ると、離型性の高い熱軟化層上に塗設された着色
感光層の上に、塗布シートの裏面<PET面)が積み重
なり、巻き押しつけられることになり、わずかでも溶剤
が残留しているε容易に、着色感光層がPET面に転写
してしまい、着色感光層の欠落(プロソキング)を生じ
る。また、このようなプロソキングを防ぐために塗工時
の乾燥温度を上げると、今度は、熱軟化層が溶融し、着
色感光層との界面で一部が混合し、それが、現像後の印
刷版の非画像部に汚れ(地汚れ)を発生させるという課
題を有している。Examples of methods for creating multicolor transfer images using color sheets for color proofing include the direct transfer method described in Japanese Patent Laid-Open No. 47-41830, in which a colored image is directly transferred and laminated onto a final image-receiving paper; As described in Japanese Patent Application Laid-Open No. 59-97140,
An indirect transfer method in which a colored image is temporarily transferred onto a temporary image-receiving sheet, and a process of forming an image after transferring a colored photosensitive layer to an image-receiving paper described in Japanese Patent Application Laid-Open No. 56-501217 is repeated. Examples include methods. In both of these methods, the surface of the transfer material on which the image is formed is coated with an organic polymer layer, so the resulting image surface is too glossy, giving an impression that the image quality is different from the actual image quality. Therefore, in order to solve this problem, an image-only transfer method was devised in which only a colored image is transferred and laminated onto a transfer material to form a multicolor image. Since this method does not coat the transferred material with an organic polymer layer, in principle it is possible to obtain an image that is very close to the image quality of actual printing. Problems to be Solved by the Invention> However, in the case of a colored image sheet used in the image-only transfer method, in order to easily transfer only the image from the heat-softening layer to the transfer sheet during the heat lamination process, the colored photosensitive layer is Decrease adhesion between and heat-softened layer (increase releasability)
There is a need. Therefore, after coating and drying the colored photosensitive layer on the heat-softening layer, when the colored photosensitive layer coating sheet is wound up as usual, the colored photosensitive layer is coated on the heat-softening layer with high mold releasability. The back side of the coating sheet <PET side> is piled up and rolled onto the colored photosensitive layer, and if there is even a small amount of solvent remaining, the colored photosensitive layer is easily transferred to the PET side, causing coloring. This results in chipping of the photosensitive layer (prosoking). In addition, if the drying temperature during coating is increased to prevent such prosoking, the heat-softened layer will melt and some of it will mix at the interface with the colored photosensitive layer, which will cause the printing plate to dry after development. There is a problem that stains (background stains) occur in the non-image areas of the image.
〈諜題を解決するための手段〉
そこで本発明者らは、上記の課題の改良された着色画像
形成材料の製造方法を提供すべく鋭意検討した結果、着
色感光層を塗工後、巻き取る際に、該着色感光層に対し
て離型性の高いシートをプロソキング防止シートとして
用い、着色感光層上に挟み込みながら巻き取ることによ
って、巻き出し時のプロンキング及び地汚れの生じにく
い着色画像形成材料の製造方法を見出し、本発明を完或
するに至った.
すなわち本発明の目的はプロツキングや地汚れの生じに
くい着色画像形成シ一トの製造方法を提供することにあ
る。<Means for Solving the Problem> The inventors of the present invention have conducted intensive studies to provide a method for producing a colored image forming material that solves the above-mentioned problems. In this case, a sheet with high releasability for the colored photosensitive layer is used as a prosoking prevention sheet and is rolled up while sandwiching it on the colored photosensitive layer, thereby forming a colored image that is less likely to cause pronking or scumming during unwinding. We discovered a method for manufacturing the material and completed the present invention. That is, an object of the present invention is to provide a method for producing a colored image forming sheet that is less likely to cause blocking or scumming.
そして、かかる本発明の目的は、支持体上に、熱軟化層
と感光性組底物及び着色剤を含有する着色感光層とをこ
の順に有する着色画像形成材料であって、像様露光及び
現像処理により形成される着色画像部のみを被転写材料
に転写して着色画像を形戊するための着色画像形成材料
の製造方法において、該熱軟化層上に着色感光層を塗布
し、乾燥させた後、得られる着色画像形成材料を巻き取
る際に、着色感光層上に該着色感光層に対して離型性を
有するシートを挟み込むこεにより達或される。The object of the present invention is to provide a colored image-forming material having, on a support, a heat-softening layer, a colored photosensitive layer containing a photosensitive composite material, and a coloring agent in this order, which can be subjected to imagewise exposure and development. In a method for producing a colored image forming material for forming a colored image by transferring only the colored image area formed by processing to a transfer material, a colored photosensitive layer is coated on the heat-softening layer and dried. Thereafter, when the obtained colored image-forming material is wound up, a sheet having releasability to the colored photosensitive layer is sandwiched over the colored photosensitive layer by ε.
以下、本発明を詳細に説明する。The present invention will be explained in detail below.
本発明に使用される透明支持体は特に限定されないが、
二輪延伸されたポリエチレンテレフタレートフィルムが
、熱に対する寸法安定性の点で好ましい。しかし、アセ
テートフィルム、ポリ塩化ビニルフィルム、ボリスチレ
ンフィルム、ボリブロピレンフィルム、ポリエチレンフ
イルム等モ使用し得る。The transparent support used in the present invention is not particularly limited, but
A two-wheel stretched polyethylene terephthalate film is preferred in terms of dimensional stability against heat. However, acetate film, polyvinyl chloride film, polystyrene film, polypropylene film, polyethylene film, etc. may also be used.
透明支持体の厚さは10〜300μmの範囲が適当であ
り、特に好ましくは25〜200μmの範囲である.
本発明に使用される熱軟化層は、次に挙げるような60
〜140℃、好ましくは70〜100゜Cの軟化点を有
する皮膜形戒性の熱可塑性樹脂が用いられる。The thickness of the transparent support is suitably in the range of 10 to 300 μm, particularly preferably in the range of 25 to 200 μm. The heat-softening layer used in the present invention is as follows:
A film-forming thermoplastic resin having a softening point of ~140°C, preferably 70-100°C is used.
例えば、特開昭1−155349号公報に記載のエチレ
ンと酢酸ビニルの共重合体、エチレンとアクリル酸エス
テルの共重合体、特開昭1−102546号公報及び特
開昭64−90437号公報に記載の脂環族飽和炭化水
素、及びスチレン共重合体等が挙げられる。特に、スチ
レン共重合体が好ましく、その具体的な例としては、三
洋化戒工業社製1ハイマーST− 9 5 ’″“ハイ
マーST−120’″,PICCO社製“ビコラスチッ
ク”オリゴスチレンにスルホン酸基を導入した巴川製紙
所製“オリゴーZ“,脂環式飽和炭化水素基を有する樹
脂としては荒川化学工業社製“アルコンPシリーズ、M
シリーズ”等が挙げられる。For example, the copolymer of ethylene and vinyl acetate, the copolymer of ethylene and acrylic acid ester described in JP-A No. 1-155349, the copolymer of ethylene and acrylic ester described in JP-A-1-102546 and JP-A-64-90437, Examples include the alicyclic saturated hydrocarbons and styrene copolymers described above. In particular, styrene copolymers are preferred, and specific examples thereof include 1Hymer ST-95'''Hymer ST-120''' manufactured by Sanyo Kakai Kogyo Co., Ltd., and ``Bicolastic'' manufactured by PICCO Co., Ltd. “Oligo Z” manufactured by Tomoekawa Paper Mills into which acid groups have been introduced, and “Alcon P series” manufactured by Arakawa Chemical Industry Co., Ltd., M as resins having alicyclic saturated hydrocarbon groups.
Series” etc.
熱軟化層の厚さは、1〜100μmの範囲が適当であり
、特に好ましくは2〜60μmの範囲である。本発明で
は、この熱軟化層の上に着色感光層を設けるが、これは
熱軟化層上に直接積層する場合のみでなく、場合により
何らかの目的で設けられた中間層を介して間接的に積層
する場合を包含する。この様な中間層としては最も典型
的には着色感光層の転写性を高める目的で、設けられる
離型層をあげることができる。その具体例としては例え
ば、特願昭63−328175号公報に記載のシリコー
ン樹脂、フッ素系界面活性剤、ポリオレフィン、ポリア
ミド等を用いることができる。The thickness of the thermally softened layer is suitably in the range of 1 to 100 μm, particularly preferably in the range of 2 to 60 μm. In the present invention, a colored photosensitive layer is provided on the heat-softening layer, but this can be done not only by directly laminating it on the heat-softening layer, but also by laminating it indirectly through an intermediate layer provided for some purpose. This includes cases where The most typical example of such an intermediate layer is a release layer provided for the purpose of improving the transferability of the colored photosensitive layer. As specific examples thereof, silicone resins, fluorosurfactants, polyolefins, polyamides, etc. described in Japanese Patent Application No. 63-328175 can be used.
また、該離型層は、必要に応じてUV、あるいは熱硬化
させることが出来る。Furthermore, the release layer can be cured by UV or heat, if necessary.
離型層の厚さは、0.05〜2μが好ましい。The thickness of the release layer is preferably 0.05 to 2μ.
本発明において着色感光層に含まれる感光性組成物とし
ては種々のものが使用可能であるが、活性光線の照射を
受けると短時間のうちにその分子構造に化学的な変化を
きたし、溶媒に対する溶解性が変化し、ある種の溶媒を
適用した場合には、露光部分又は非露光部分が溶解除去
してしまうようなモノマー、ブレボリマー又はボリマー
などの化合物のすべてが含まれる。使用可能な感光性組
戒物の例としては、露光部の溶解性が低下する、いわゆ
るネガ、ポジタイプのものとして、ポリビニルアルコー
ルをケイ皮酸でエステル化したもので代表される光架橋
型の感光性樹脂系:ジアゾニウム塩やその縮合体をポリ
ビニルアルコール、ポリビニルピロリドン、ポリアクリ
ルアξド等と混合した系:また芳香族アジド化合物を光
架橋剤として用い環化ゴム等のバインダーと混合した系
等があり、さらに光ラジカル重合や光イオン重合を利用
した感光性樹脂も用いることができる。また露光部の溶
解性が増大する、いわゆるポジ・ボジタイプのものとし
ては例えば、0−キノンジアジドを感光性物質とする感
光性樹脂組或物があり、具体的には1,2−ペンゾキノ
ンジアジド−4−スルホニルクロライド、1.2−ナフ
トキノンジアジド−4−マニホニルクロライド、1.2
−ナフトキノンジアジド−5−スルホニルクロライド、
1.2−ナフトキノンジアジド−6−スルホニルクロラ
イドと水酸基及び/又はアミノ基含有化合物を縮合させ
た化合物が好まし《用いられる.上記水酸基含有化合物
としては、例えばトリヒド口キシベンゾフエノン、ジヒ
ドロキシアントラキノン、ビスフェノールA1フェノー
ルノボラック樹脂、レゾルシンベンズアルデヒド縮合樹
脂、ビロガロールアセトン縮合樹脂等がある。また、上
記アミノ基含有化合物としては、例えばアニリン、p−
アミノジフエニルアミン、p−アミノベンゾフエノン、
4,4′−ジアミノジフエニルアξン、4,4−ジア旦
ノベンゾフエノン等がある。In the present invention, various photosensitive compositions can be used as the photosensitive composition contained in the colored photosensitive layer, but when irradiated with actinic rays, the molecular structure undergoes a chemical change within a short period of time, making it difficult to react to the solvent. All compounds such as monomers, brevolimers or polymers whose solubility changes and whose exposed or unexposed portions are dissolved away when certain solvents are applied are included. Examples of photosensitive compositions that can be used include photocrosslinking type photosensitive materials, such as those made by esterifying polyvinyl alcohol with cinnamic acid, which are so-called negative and positive types that reduce the solubility of exposed areas. Resin system: A system in which a diazonium salt or its condensate is mixed with polyvinyl alcohol, polyvinylpyrrolidone, polyacrylamide, etc.: A system in which an aromatic azide compound is used as a photocrosslinking agent and mixed with a binder such as cyclized rubber, etc. In addition, photosensitive resins using photoradical polymerization or photoionic polymerization can also be used. In addition, examples of so-called positive-positive type materials that increase solubility in exposed areas include photosensitive resin compositions containing 0-quinonediazide as a photosensitive substance, specifically 1,2-penzoquinonediazide- 4-sulfonyl chloride, 1.2-naphthoquinonediazide-4-manifonyl chloride, 1.2
-naphthoquinonediazide-5-sulfonyl chloride,
1. A compound obtained by condensing 2-naphthoquinonediazide-6-sulfonyl chloride with a compound containing a hydroxyl group and/or an amino group is preferably used. Examples of the above-mentioned hydroxyl group-containing compounds include trihydroxybenzophenone, dihydroxyanthraquinone, bisphenol A1 phenol novolac resin, resorcin benzaldehyde condensation resin, and birogallol acetone condensation resin. Further, examples of the amino group-containing compound include aniline, p-
aminodiphenylamine, p-aminobenzophenone,
Examples include 4,4'-diaminodiphenylamane, 4,4-diaminobenzophenone, and the like.
上記0−キノンジアジド化合物に関しては、さらにJ,
KOSAR著” Light Sensitive
System(Wiley & Sons, New
York+ 1 9 6 5 )および永松,乾著“感
光性高分子” (講談社.1977)に記載のものも用
いることができる.
さらにボジ・ポジタイブのものとして、i)活性光線の
照射により酸を発生し得る化合物、ii )酸により分
解し得る結合を少なくとも1個有する化合物、およびi
ii)2または3種類の異なるフェノール類を含むノボ
ラック樹脂、を含有する感光性樹脂m或物を用いること
もできる。Regarding the above 0-quinonediazide compound, J,
“Light Sensitive” by KOSAR
System(Wiley & Sons, New
York+ 1965) and those described in "Photosensitive Polymers" by Inui Nagamatsu (Kodansha, 1977) can also be used. Furthermore, as positive and positive compounds, i) compounds that can generate an acid upon irradiation with actinic rays, ii) compounds that have at least one bond that can be decomposed by an acid, and i
It is also possible to use photosensitive resins containing ii) novolac resins containing two or three different phenols.
着色感光層中における上記感光性組或物の含有量は、例
えば重量で5〜80%が適当である。The content of the photosensitive composition in the colored photosensitive layer is, for example, 5 to 80% by weight.
また、前記着色感光層を構或する結合剤としては、皮膜
形成性かつ溶媒可溶性であり、好ましくはアルカリ現像
液で溶解ないし、膨潤しうる高分子化合物が用いられる
。Further, as the binder constituting the colored photosensitive layer, a polymer compound is used which is film-forming and solvent-soluble, and preferably dissolves or swells in an alkaline developer.
かかる高分子化合物の具体例としては、例えば特開平1
−99048号公報に記載のN一(4 −ヒドロキシフ
ェニル)−(メタ)アクリルア累ドを有する高分子化合
物、具体的にはN−(4−ヒドロキシフェニル)一アク
リルアミド、アクリロニトリル、アクリル酸メチルとの
共重合体、また、特開昭55−57841,同55−1
27553号公報記載のノボラック樹脂等が挙げられる
。Specific examples of such polymer compounds include, for example, Japanese Patent Application Laid-Open No.
Polymer compounds having N-(4-hydroxyphenyl)-(meth)acrylates described in Publication No. 99048, specifically N-(4-hydroxyphenyl)-monoacrylamide, acrylonitrile, and methyl acrylate. Copolymer, also JP-A-55-57841, JP-A-55-1
Examples include novolac resins described in Japanese Patent No. 27553.
該高分子化合物の含有量は、重量で20〜80%が適当
である.
前記着色感光層中には、着色剤として染料、顔料が添加
される。例えば特開平1−99048号公報記載のもの
が挙げられる。The content of the polymer compound is suitably 20 to 80% by weight. In the colored photosensitive layer, dyes and pigments are added as colorants. For example, those described in JP-A-1-99048 can be mentioned.
着色感光層中における着色剤の含有量は重量で5%〜5
0%が適当である。The content of the colorant in the colored photosensitive layer is 5% to 5% by weight.
0% is appropriate.
着色感光層の着色剤/結合剤の比率は、目標とする光学
濃度と着色感光層の現像液に対する.除去性を考慮して
同業者に公知の方法により定めることができる。例えば
、染料の場合、その値は重量で5%〜75%、顔料の場
合、その値は重量で5%〜90%が適当である。The colorant/binder ratio of the colored photosensitive layer is determined based on the target optical density and the developer of the colored photosensitive layer. It can be determined by a method known to those skilled in the art in consideration of removability. For example, in the case of dyes, the appropriate value is 5% to 75% by weight, and in the case of pigments, the value is 5% to 90% by weight.
前記着色画像形成材料は、特願昭62−261)29号
公報と同様の方法で、像様露光し、アルカリ性現像液で
現像して着色画像を形成する.次に、得られた着色画像
をアート紙、コート祇゛等の被転写材料に転写する。具
体的には、着色画像層と被転写材料の表面とを重ね合せ
、加熱・加圧下でラミネーターを通過させる.ラミネー
ターの条件としては、通常、加熱温度が70〜150℃
、通過速度が50〜IOOCII/分の範囲が適当であ
る。かかるラミネーター通過時の加熱・加圧により、着
色画像部が被転写材料表面に融着し、転写、積層される
。The colored image forming material is imagewise exposed and developed with an alkaline developer to form a colored image in the same manner as in Japanese Patent Application No. 62-261)29. Next, the obtained colored image is transferred to a transfer material such as art paper or coated paper. Specifically, the colored image layer and the surface of the transfer material are overlapped and passed through a laminator under heat and pressure. The laminator conditions are usually a heating temperature of 70 to 150°C.
, it is appropriate for the passing speed to be in the range of 50 to IOOCII/min. By heating and applying pressure when passing through the laminator, the colored image portion is fused to the surface of the transfer material, and transferred and laminated.
前記熱軟化層を支持体上に塗設するための塗布方法とし
ては、ブレードコーティング,リバースロールコーティ
ング,グラビアコーティング,ロンドコーティング,グ
イコーティング,ラミネート法等の方法が用いられる.
該、熱軟化層塗設支持体上に前記着色感光層を塗設する
ための塗布方法としては、ロールコーティング.リバー
スロールコーティング.グラビアコーティング,ダイコ
ーティング等の方法が用いられる。また、着色感光層の
乾燥は、地汚れの原因となる着色感光層と熱軟化層との
混合を防ぐため、加熱温度は30℃〜100℃が好まし
く、特に40℃〜90℃の範囲が好適である。乾燥中、
加熱された空気の温度を一定に保ったまま着色感光層を
乾燥させる方法が一般に行なわれているが、加熱された
空気の温度を段階的に上昇させて乾燥させる方法も1テ
なうことができる。また、乾燥時間は30秒間〜10分
間の範囲が好適である。As a coating method for coating the heat-softening layer on the support, methods such as blade coating, reverse roll coating, gravure coating, rondo coating, gooey coating, and laminating methods are used. The coating method for coating the colored photosensitive layer on the heat softening layer coated support includes roll coating. Reverse roll coating. Methods such as gravure coating and die coating are used. In addition, when drying the colored photosensitive layer, the heating temperature is preferably 30°C to 100°C, particularly preferably 40°C to 90°C, in order to prevent mixing of the colored photosensitive layer and the heat-softened layer, which may cause scumming. It is. During drying,
The commonly used method is to dry the colored photosensitive layer while keeping the temperature of the heated air constant, but it is also possible to dry the colored photosensitive layer by increasing the temperature of the heated air in stages. can. Further, the drying time is preferably in the range of 30 seconds to 10 minutes.
さらに、着色感光層が塗布、乾燥されたシートの巻き取
りは、着色感光層のプロフキングを防ぐ目的で、着色感
光層上に該着色感光層に対し離型性を有するシ一ト(ブ
ロンキング防止シート〉を挟み込んだ状態で巻き取られ
る。Furthermore, when winding up the sheet on which the colored photosensitive layer has been coated and dried, a sheet (bronching) having mold release properties for the colored photosensitive layer is placed on the colored photosensitive layer for the purpose of preventing profking of the colored photosensitive layer. The film is wound up with the "preventive sheet" sandwiched in between.
該着色感光層塗設シ一トを巻き取る際に、巻き取られる
若色感光層の残留溶剤量としては、重量で10%以下が
好ましく、さらに好ましくは、5%以下である。また、
巻きとり速度としては、1m/分〜70m/分が好まし
く、特に3m/分〜50m/分の範囲が好適である。ま
た、巻きとり張力としては、0. 0 2 〜0. 4
kg/cmが好ましく、特に好ましくは、0.04
〜0.3kg/amの範囲である,
本発明で使用されるブロッキング防止シートとしては、
少くともその表面が着色感光層に対して離型性を有する
物である,例えば、単独材料のものとしては、表面の離
型性が高いプラスチ・ノクシー1・等が好適で、具体的
には、ポリプロピレンシ一ト、ポリエチレンシ一ト、テ
フロンシ一ト、ポリビニルアルコールシ一ト、等が挙げ
られる.また、複合化材料のものとしては、離型処理プ
ラスチック、紙、等が挙げられる,具体的には、シリコ
ーンコートポリエチレンテレフタレートシ一ト、ポリエ
チレンラミネートポリエチレンテレフタレートシート、
シリコーンコー1・紙、ポリエチレンラξネート祇等が
挙げられる。これらのシートは必要に応じて、エンボス
、マント化処理あるいは多多孔質、不織布のような形状
にすることが出来る。When the colored photosensitive layer coating sheet is wound up, the amount of residual solvent in the young photosensitive layer to be wound up is preferably 10% or less by weight, more preferably 5% or less. Also,
The winding speed is preferably 1 m/min to 70 m/min, particularly preferably 3 m/min to 50 m/min. Moreover, the winding tension is 0. 0 2 ~ 0. 4
kg/cm is preferred, particularly preferably 0.04
The anti-blocking sheet used in the present invention is in the range of ~0.3 kg/am.
At least the surface of the material has mold releasability with respect to the colored photosensitive layer.For example, as a single material, Plasti Noxy 1, etc., which have a high surface mold releasability, is suitable.Specifically, , polypropylene sheet, polyethylene sheet, Teflon sheet, polyvinyl alcohol sheet, etc. In addition, examples of composite materials include release-treated plastics, paper, etc. Specifically, silicone coated polyethylene terephthalate sheets, polyethylene laminated polyethylene terephthalate sheets,
Examples include silicone coat 1, paper, and polyethylene laminate. These sheets can be embossed, cloaked, porous, nonwoven-like, etc., as desired.
また、プロソキング防止シートの膜厚としては10um
〜1000μmの範囲が好適である。In addition, the thickness of the anti-prosoking sheet is 10um.
A range of 1000 μm is preferable.
以下、本発明を実施例並びに比較例により更に詳細に説
明するが、本発明はこれら実施例に限定されるものでは
ない。EXAMPLES Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.
実施例1
厚さ75μmのポリエチレンテレフタレートフィルム上
に厚さ25μmになるように下記U或の熱軟化層溶液を
、グイコーターにより塗布した。Example 1 A heat-softening layer solution (U) below was coated onto a polyethylene terephthalate film having a thickness of 75 μm to a thickness of 25 μm using a Goocoater.
次に、該熱軟化層上に、リバースロールコーターにより
、下記組或の着色感光層分散液(A)を乾燥膜厚が1.
5μmになるように塗布した.着色感光層分散液(A)
なお、アルカリ可溶性高分子組成物は下記の方法で合威
した.
容量l1の四つロフラスコに、ヒドロキシフエニルメタ
クリルアミド8.85g,アクリロニトリル2.65g
,メチルアクリレート33.1)g,アブビスイソブチ
ロニトリル(重合開始剤)1.64gを秤量し、200
gのエチルアルコールを溶媒とし、77℃で6時間反応
させた.この後、メチルセロソルブを75g加え、反応
を停止させ、60℃にて3時間エチルアルコールを留去
した。Next, a colored photosensitive layer dispersion (A) of the following set was applied onto the heat-softened layer using a reverse roll coater to a dry film thickness of 1.
It was applied to a thickness of 5 μm. Colored photosensitive layer dispersion (A) The alkali-soluble polymer composition was prepared in the following manner. In a four-bottle flask with a capacity of 11, 8.85 g of hydroxyphenyl methacrylamide and 2.65 g of acrylonitrile were added.
, 33.1) g of methyl acrylate, and 1.64 g of abbisisobutyronitrile (polymerization initiator),
g of ethyl alcohol was used as a solvent, and the reaction was carried out at 77°C for 6 hours. Thereafter, 75 g of methyl cellosolve was added to stop the reaction, and ethyl alcohol was distilled off at 60° C. for 3 hours.
次に、乾燥温度70℃2分間により乾燥後、厚さ25μ
mのボリプロビレンシ一トを感光層上に重ね合わせ0.
0 7 kg/ctaの巻き取り張力で巻き取った。Next, after drying at a drying temperature of 70°C for 2 minutes, a thickness of 25 μm was obtained.
0.m of polypropylene is superimposed on the photosensitive layer.
It was wound up with a winding tension of 0.7 kg/cta.
該、巻き取られたコイルから、着色感光シートを巻き出
した所、プロッキングはまったく発生しなかった。When the colored photosensitive sheet was unwound from the wound coil, no blocking occurred at all.
以上により得られた4色の着色画像形成材料に各色の色
分解網フィルムを重ね合わせ、4kWメタルハライドラ
ンプで1mの距離から40秒間画像露光を行い、下記現
像液に30秒間浸漬することにより現像を行ったところ
、非画線部の地汚れがまったく無いきれいな4色の着色
画像を形成した。The color separation mesh film of each color was superimposed on the four colored image forming materials obtained above, imagewise exposed for 40 seconds from a distance of 1 m using a 4kW metal halide lamp, and developed by immersing it in the following developer for 30 seconds. As a result, a clean four-color colored image was formed with no background stains in the non-image areas.
里盈直
SDR−1 (ボジps版用現像液,コニカ社製)
20g
界面活性剤(ペレックスNBL,
花王アトラス社製) 50g
蒸留水 400g次にイエ
ローの着色画像シートの画像面とアート祇とを密着し、
80℃に加熱された1対のニップロール間を5kg/c
aa”の加圧条件下にて50an/分の速度で通過させ
ることにより、アート紙上にイエロー着色画像の転写を
行い、着色画像側の支持体を剥離した。引き続き、マゼ
ンタ、シアン、ブラックの順に、着色画像の転写を行い
、アート紙上に4色から或る極めて印刷画像に近似した
カラー画像が形成された。Riei Nao SDR-1 (Developer for Boji PS plate, manufactured by Konica)
20g surfactant (Perex NBL, manufactured by Kao Atlas Co., Ltd.) 50g distilled water 400gNext, the image surface of the yellow colored image sheet and Art Gi were brought into close contact,
5kg/c between a pair of nip rolls heated to 80℃
A yellow colored image was transferred onto art paper by passing at a speed of 50 an/min under a pressure condition of "aa", and the support on the colored image side was peeled off.Subsequently, magenta, cyan, and black were transferred in the order of magenta, cyan, and black. , a colored image was transferred, and a color image very similar to a printed image was formed from four colors on art paper.
また、該着色感光シートコイルを1週間室温で放置した
後、着色感光シートを巻き出した所、まったくプロソキ
ングは発生していなかった。Further, when the colored photosensitive sheet coil was left at room temperature for one week and then unwound, no prosoking occurred.
実施例2
実施例1において、着色感光層分散液(A)を下記の着
色感光層分散液(B)に変更した以外は、まったく同様
に塗布、乾燥し、40μ閑のポリエチレンシ一トを感光
層上に重ね合わせて実施例lと同様にして巻き取った。Example 2 Coating and drying were carried out in exactly the same manner as in Example 1, except that the colored photosensitive layer dispersion (A) was changed to the following colored photosensitive layer dispersion (B), and a 40μ blank polyethylene sheet was exposed to light. The layers were superimposed and wound up in the same manner as in Example 1.
咳巻き取ったコイルから着色感光シートを巻き出した所
、まったくプロッキングは発生しなかった。また、実施
例1と同様に露光・現像処理した所、地汚れの無い良好
な4色着色画像シートが得られ、アート紙に積層転写し
た所、印刷物近似のカラー画像が形成された。When the colored photosensitive sheet was unwound from the coil that had been wound up, no blocking occurred at all. Further, when exposed and developed in the same manner as in Example 1, a good four-color colored image sheet with no background smear was obtained, and when laminated and transferred to art paper, a color image similar to that of a printed matter was formed.
着色感光層分散液(B)
下記組戒のアルカリ可溶性高分子
&Ilrfc物(重量平均分子量17,000,50%
メチルセロソルブ溶液) 12g0H
(l :m:n=1(1)0:80)
ペンタエリスリトールテトラ
アクリレート 4.3gミヒラ
ーズケトン 0。04gペンゾフェ
ノン 0.25gバラメトキシ
フユノール 0.01gメチルセロソルブ
94gフッ素系界面活性剤
<3M社製,FC−430) 0.01g下
記顔料
(頗料)
ブラック:カーボンブラックMA− 1 0 0(三菱
化威製) 1. 9 8 gシアン :シ
アニンブル−4920
(大日精化製) 1. 1 0 gマゼン
タ:セイ力ファースト
カーミン1483
(大日精化製) 1.36gイエロー:セ
イカファースト
イエロー2400
(大日精化製) 1.36g実施例3
実施例1において、着色感光層分散?Fl.(A)を下
記の着色感光層分散液(C)に変更した以外は、まった
く同様に、塗布、乾燥を行ない、20μmのシリコーン
コート紙を感光層上にシリコーン面が感光層と密着する
ように重ね合わせ巻き取りを行った.
該巻き取ったコイルから着色感光シートを巻き出した所
、まったくプロソキングは発生しなかった。また、実施
例1と同様に露光、現像処理を施した所、地汚れのない
良好な4色着色画像シートが得られ、アート紙に積層転
写した所、印刷物近似の美しいカラー画像が形成された
。Colored photosensitive layer dispersion (B) Alkali-soluble polymer & Ilrfc material of the following composition (weight average molecular weight 17,000,50%)
Methyl cellosolve solution) 12g0H (l:m:n=1(1)0:80) Pentaerythritol tetraacrylate 4.3g Michler's ketone 0.04g Penzophenone 0.25g Paramethoxyfuunol 0.01g Methyl cellosolve 94g Fluorine surfactant <Manufactured by 3M Company, FC-430) 0.01g The following pigments (black pigment) Black: Carbon black MA-100 (manufactured by Mitsubishi Kawei) 1. 9 8 g Cyanide: Cyanine Blue-4920 (manufactured by Dainichiseika) 1. 10 g Magenta: Seiroku First Carmine 1483 (manufactured by Dainichiseika) 1.36 g Yellow: Seika First Yellow 2400 (manufactured by Dainichiseika) 1.36 g Example 3 In Example 1, colored photosensitive layer dispersion? Fl. Coating and drying were carried out in exactly the same manner except that (A) was changed to the following colored photosensitive layer dispersion (C), and 20 μm silicone coated paper was placed on the photosensitive layer so that the silicone surface was in close contact with the photosensitive layer. Overlapping winding was performed. When the colored photosensitive sheet was unwound from the wound coil, no prosoking occurred. Further, when exposure and development were performed in the same manner as in Example 1, a good four-color colored image sheet with no background stains was obtained, and when layered and transferred onto art paper, a beautiful color image similar to that of printed matter was formed. .
着色感光層分散液(C)
下記組或のアルカリ可溶性高分子
U戒物(重量平均分子量17,000.50%メチルセ
ロソルブ溶液) 12g0H
(J’:m:n=10:10:80)
N!CP
下記顔料
(顔料)
ブラック二カーボンブラックMA
(三菱化戒製)
シアン :シアニンブル−4920
(大日精化製)
マゼンタ:セイ力ファースト
カーミン1483
(大日精化製)
イエロー:セイ力ファースト
イエロー2400
(大日精化製)
1.9
0g
1. 3
1. 3 6 g
比較例1
感光層塗設済シートを巻きとる時に、プロソキング防止
シートを挾み込まないこと以外は、実施例1と同様にし
て感光層塗設シ一トの巻き取りコイルを得た。該コイル
から着色感光シートを巻き出した所、感光層はプロソキ
ングを起こし、部分的に欠落を生じた。Colored photosensitive layer dispersion (C) A certain alkali-soluble polymer U compound of the following composition (weight average molecular weight 17,000.50% methyl cellosolve solution) 12g0H (J':m:n=10:10:80) N! CP The following pigments (pigments) Black Carbon Black MA (manufactured by Mitsubishi Kakai) Cyan: Cyanine Blue-4920 (manufactured by Dainichiseika) Magenta: Seiriki First Carmine 1483 (manufactured by Dainichiseika) Yellow: Seiriki First Yellow 2400 (manufactured by Dainichiseika) (manufactured by Nisseika) 1.9 0g 1. 3 1. 3 6 g Comparative Example 1 A winding coil of a photosensitive layer coated sheet was obtained in the same manner as in Example 1 except that the anti-prosoking sheet was not inserted when winding up the photosensitive layer coated sheet. . When the colored photosensitive sheet was unwound from the coil, the photosensitive layer suffered from prossoking and was partially chipped.
比較例2
実施例1において乾燥条件を70℃から1)0℃に変更
した以外は、まったく同様にして感光層塗設シ一トの巻
き取りコイルを得た。Comparative Example 2 A winding coil of a photosensitive layer coated sheet was obtained in exactly the same manner as in Example 1 except that the drying conditions were changed from 70°C to 1) 0°C.
該コイルから、着色感光シートを巻き出した所、感光層
のプロソキングは発生しなかった。このシートを実施例
1と同様に露光・現像処理を施した所、非画線部に、地
汚れを生じた。When the colored photosensitive sheet was unwound from the coil, no prosoking of the photosensitive layer occurred. When this sheet was exposed and developed in the same manner as in Example 1, scumming occurred in the non-image areas.
また、該コイルを1週間室温放置した後、着色感光シー
トを巻き出した所、プロッキングが起こり、部分的に感
光層の欠落を生じた。Furthermore, when the colored photosensitive sheet was unwound after the coil was left at room temperature for one week, blocking occurred and the photosensitive layer was partially missing.
〈発明の効果〉
以上詳しく説明したように、本発明の着色画像形成材料
の製造法により、プロソキング、および地汚れの発生し
ない着色画像形成材料を得ることができた。<Effects of the Invention> As explained in detail above, by the method for producing a colored image forming material of the present invention, it was possible to obtain a colored image forming material free from prosoking and scumming.
出 願 人 三菱化或株式会社 代 理 人Out wish Man Mitsubishi Kaoru Co., Ltd. teenager Reason Man
Claims (1)
色剤を含有する着色感光層とをこの順に有する着色画像
形成材料であって、像様露光及び現像処理により形成さ
れる着色画像部のみを被転写材料に転写して着色画像を
形成するための着色画像形成材料の製造方法において、
該熱軟化層上に着色感光層を塗布し、乾燥させた後、得
られる着色画像形成材料を巻き取る際に、着色感光層上
に、該着色感光層に対して離型性を有するシートを挟み
込むことを特徴とする着色画像形成材料の製造方法。(1) A colored image-forming material having a heat-softening layer and a colored photosensitive layer containing a photosensitive composition and a colorant in this order on a transparent support, the colored image forming material being formed by imagewise exposure and development treatment. In a method for producing a colored image forming material for forming a colored image by transferring only the image area to a transfer material,
After coating the colored photosensitive layer on the heat-softening layer and drying it, when winding up the obtained colored image forming material, a sheet having mold release properties for the colored photosensitive layer is coated on the colored photosensitive layer. A method for producing a colored image forming material, characterized by sandwiching the material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19166489A JPH0355550A (en) | 1989-07-25 | 1989-07-25 | Production of colored image forming material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19166489A JPH0355550A (en) | 1989-07-25 | 1989-07-25 | Production of colored image forming material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0355550A true JPH0355550A (en) | 1991-03-11 |
Family
ID=16278404
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19166489A Pending JPH0355550A (en) | 1989-07-25 | 1989-07-25 | Production of colored image forming material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0355550A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0543146U (en) * | 1991-11-07 | 1993-06-11 | 東洋インキ製造株式会社 | Photosensitive ink sheet |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59159155A (en) * | 1983-03-01 | 1984-09-08 | Hitachi Chem Co Ltd | Photosensitive resin composition |
JPS59202457A (en) * | 1983-05-02 | 1984-11-16 | Asahi Chem Ind Co Ltd | Improved photopolymerizable laminate |
JPS6032045A (en) * | 1983-08-01 | 1985-02-19 | Sanyo Kokusaku Pulp Co Ltd | Multicolor image forming material and its image forming method |
JPS62204249A (en) * | 1986-03-05 | 1987-09-08 | Fuotopori Ouka Kk | Photosensitive resin laminated body |
JPH01221735A (en) * | 1988-02-29 | 1989-09-05 | Nippon Synthetic Chem Ind Co Ltd:The | Image forming method |
JPH02278263A (en) * | 1989-03-15 | 1990-11-14 | Basf Ag | Method of manufacturing photosensitive recording material and printed circuit |
-
1989
- 1989-07-25 JP JP19166489A patent/JPH0355550A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59159155A (en) * | 1983-03-01 | 1984-09-08 | Hitachi Chem Co Ltd | Photosensitive resin composition |
JPS59202457A (en) * | 1983-05-02 | 1984-11-16 | Asahi Chem Ind Co Ltd | Improved photopolymerizable laminate |
JPS6032045A (en) * | 1983-08-01 | 1985-02-19 | Sanyo Kokusaku Pulp Co Ltd | Multicolor image forming material and its image forming method |
JPS62204249A (en) * | 1986-03-05 | 1987-09-08 | Fuotopori Ouka Kk | Photosensitive resin laminated body |
JPH01221735A (en) * | 1988-02-29 | 1989-09-05 | Nippon Synthetic Chem Ind Co Ltd:The | Image forming method |
JPH02278263A (en) * | 1989-03-15 | 1990-11-14 | Basf Ag | Method of manufacturing photosensitive recording material and printed circuit |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0543146U (en) * | 1991-11-07 | 1993-06-11 | 東洋インキ製造株式会社 | Photosensitive ink sheet |
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