GB2229286A - Method of forming a reversed image - Google Patents

Method of forming a reversed image Download PDF

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Publication number
GB2229286A
GB2229286A GB8905742A GB8905742A GB2229286A GB 2229286 A GB2229286 A GB 2229286A GB 8905742 A GB8905742 A GB 8905742A GB 8905742 A GB8905742 A GB 8905742A GB 2229286 A GB2229286 A GB 2229286A
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United Kingdom
Prior art keywords
water
poly
soluble
image
vinyl
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Granted
Application number
GB8905742A
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GB2229286B (en
GB8905742D0 (en
Inventor
Norio Yabe
Hideaki Sasaki
Kuniaki Monden
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Sanyo Kokusaku Pulp Co Ltd
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Sanyo Kokusaku Pulp Co Ltd
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Publication of GB8905742D0 publication Critical patent/GB8905742D0/en
Publication of GB2229286A publication Critical patent/GB2229286A/en
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Publication of GB2229286B publication Critical patent/GB2229286B/en
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/016Diazonium salts or compounds
    • G03F7/021Macromolecular diazonium compounds; Macromolecular additives, e.g. binders
    • G03F7/0212Macromolecular diazonium compounds; Macromolecular additives, e.g. binders characterised by the polymeric binder or the macromolecular additives other than the diazo resins or the polymeric diazonium compounds
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/008Azides
    • G03F7/012Macromolecular azides; Macromolecular additives, e.g. binders
    • G03F7/0125Macromolecular azides; Macromolecular additives, e.g. binders characterised by the polymeric binder or the macromolecular additives other than the macromolecular azides
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/26Processing photosensitive materials; Apparatus therefor
    • G03F7/38Treatment before imagewise removal, e.g. prebaking

Description

4 TITLE: Method of Forming an Image The present invention relates to a
method of forming a positive-positive type image utilizable mainly for the printing plate-making material, duplicating material, etc. and, in more detail, relates to a method of forming an image having no colouring originating from water-soluble photo- crossl inking agent without using the development chemicals except water.
As the conventional positive-positive type photosensitive compositions and the methods of.f.orming an image used these compositions, there have been, (1) System of a composition comprising o-quinone diazide compound /development with alkali or organic solvent.
This is a composition comprising o-quinone diazide and alkali-soluble or organic solvent-soluble resin such as Novolak resin and, by utilizing a phenomenon that o-quinone diazide compound changes to an alkali-soluble substance or organic solvent-soluble substance through the photodecomposition and by developing through the alkali-dissolution or organic solventdissolution, an image is formed (this can be found, for example, in Japanese Unexamined Patent Publication No. Sho 50-125806, Sho 61-5251, etc.). (2) System of a composition comprising photosensitive diazonium salt and water-soluble resin/development with alkali or ammonia.
This is a compound comprising photosensitive diazonium salt and watersoluble resins such as poly(vinyl alcohol), diacetoneacrylamideacrylamide copolymer, etc. and, by utilizing a phenomenon tha't photosensitive diazonium salt and watersoluble.re.sin give rise to the coupling reaction under alkaline atmosphere to be insolubilized into water, the non-image area is rubbed out to form an image-after immersed into alkali solution or after touched with ammonia vapor (this can be found, for example, in Japanese Unexamined Patent Publication No. Sho 56- 101141, Sho 56101144, Sho 57-72140, Sho 57-191632, etc..) 2 With these conventional image-forming methods, however, there have been following problems. Namely, since alkali solution or organic solvent is used in (1) and alkali solution is used in (2), there are apprehensions to cause-a problem on safety during the developing operation and a problem of pollution in the effluent treatment. Moreover, in (2), the development treatment with ammonia vapor is possible, but the intensive ammonia odor worsens significan'tly the environment of operation. Further, in the image formed in (1), the color of o-quinone diazide compound or decomposition products thereof is left behind and, in (2), there occurs an inherent coloring due to the coupling reaction. For these reasons, it is difficult to obtain colored images with arbitrary color in both (1) and (2), even if adding coloring agent.
The purpose of the invention is to provide a method of forming a positivepositive type image, wherein the image formation is possible by the treatment with warm water without using entirely the chemicals such as alkali, organic solvent, etc. and there are no coloring due to the photosensitive components or the decomposition products thereof and the color generation etc. caused by the image-forming reaction. SUMMARY OF THE INVENTION The gist of the invention lie's in that a photosensitive layer is formed on a substrate using a composition comprising watersoluble photo-crosslinking agent, water-soluble resin and synthetic resin emulsion and further coloring agent, if necessary, said -
1 photosensitive layer is exposed to active rays through manuscript, then this is immersed into warm water of 30 to 60 OC for not less than 3 seconds to allow the exposed area to swell and soften sufficiently-with warm water and simultaneously to allow almost all of water-soluble photocrosslinking agent in-the nonexposed area to dissolve out into warm water, and successively the swollen and softened exposed area is rubbed out to form an image having no coloring originating from water-soluble photocrosslinking agent without using the development chemicals except water. DETAILED DESCRIPTION OF THE INVENTION
As a result of diligent studies on a novel method of forming positivepositive type image possible to form an image without using entirely the chemicals such as alkali, organic solvent, etc., the inventors have found a phenomenon that the positive type photosensitive composition is obtained using the watersoluble photo-crosslinking agent (as shown, for example, in Japanese Patent Publication No. Sho 44-28725) used hitherto for negative type photosensitive composition. Namely, the phenomenon to obtain a positive image by exposing to light the photosensitive layer formed on a supporter with a composition comprising watersoluble photo- crosslinking agent, water-soluble resin and synthetic resin emulsion through a positive image manuscript, by immersing it into warm water and by rubbing it with sponge has been found. Moreover, it is a special feature that the image thus obtained has almost no coloring due to the photosensitive components or no color generation accompanied with the image-forming reaction.- 1 The mechanism of this phenomenon is considered as follows: o Exposed area Exposed to active rays, the water-soluble photo-crosslinking agent and the water-soluble resin in the photosensitive layer are crosslinked. When immersing into warm water, this photocrosslinking component swells easily to soften the photosensitive layer of this part. Also, the adhesiveness to the supporter is decreased. Consequently, this part is removed easily from supporter by rubbing with sponge etc. o Nonexposed area When immersin. into warm water, most part of the water-soluble photo- crosslinking agent and the water-soluble resin in the photosensitive layer dissolve out, but the photosensitive layer shows no changes in the swelling, softening, etc. and the adhesiveness to the supporter also does not change. Consequently, the photosensitive layer is not removed from the supporter even if rubbed with sponge. Moreover, since most part of the water-soluble photo-crosslinking agent in the photosensitive layer dissolves out, the remaining photosensitive layer is colorless.
The invention provides the positive-positive type imageforming method utilized the phenomenon as described above.
As the water-soluble photo-crosslinking agents in the photosensitive compositions to be used for the image-forming method of the invention, water-soluble azide compounds, diazonium salts, tetrazonium salts and other publicly known organic photosensitive substances can be used. Exemplifying here several kinds thereamong, They are follows.:
- 5 o Water-soluble azide compound Sodium 4,4'-diazidostilbene-2y-2'disulfonate Sodium 4'-azido-4-azidobenzalacctophenone-2-suifonate Sodium 4,4'-diazidostilbene- o-carboxylate Sodium di-(4-azido-2'hydroxybenzal)acetone-2-sulfonate Sodium 4-azidobenzalacetophenone-2sulfonate Diazo resin Condensate of p-diazodiphenylamine with formaldehyde o Tetrazonium salt Diphenyl-4,4'-bisdiazonium chloride-zinc chloride double salt 3,3'-Dimethyldiphenyl-4,4'-bisdiazonium chloride- zinc chloride double salt 3,3'-Dimethoxydimethyl-4,4'-bisdiazonium chloride.zinc chloride double salt Diphen ylamine-4,4'-bisdiazonium chloride-zinc chloride double salt Diphenylmethane-4, C-bisdiazonium chloride-zinc chloride double salt As the water-soluble resins in the photosensitive compositions to be used for the image-forming method of the invention, a lot of compounds such as polyacrylamide, poly(vinylpyrrolidone), poly(vinyl alcohol), graft-polymerization products of poly(vinyl alcohol) with vinyl monomers, water-soluble poly(vinyl butyral), glue, casein, gelatin, arabic gum, egg albumin, gums, alginic acids, poly(ethylene oxide), poly(acrylic acid) and salts thereof, poly(methacrylic acid) and salts thereof, or mixtures of these, further mixtuers of these with pdly(vinyl alcohol), cellulose derivatives such as carboxymethyleellulose, hydroxyehtylcellulose, etc., and the like can be mentioned.
As the synthetic resin emulsions in the photosensitive composi tions to be used for the image-forming method of the invention, a lot of compounds such as polyacrylate, ethylene-vinyl acetate copolymer, poly (vinylidene chloride), poly- (vinyl acetate), poly(vinyl chloride), copolymers or mixtures of these, and the like can be mentioned.
Further, to the photosensitive compositions to be used for the imageforming method of the invention, water-dispersible colored pigments,' water-soluble dyes, leveling agents, stabilizing agents, matting agents, etc., which are publicly known hitherto, can be added, if necessary.
The photosensitive composition to be used for the image-forming method of the invention comprises said water-soluble photo-crosslinking agent, water-soluble resin and synthetic resin emulsion. The formulation ratio in terms of solids of water-soluble resin to-synthetic resin emulsion is 1: 99 to 80: 20, more preferably 5: 95 to 40: 60. If too much water- soluble resin is used, the water-resistance of image is decreased resulting in dropping out of image at the time of development and, if too much synthetic resin emulsion is used, the developability is decreased. If coming off seriously said range, the image cannot be obtained.
- 7 Moreover, the formulation ratio in terms of solids of the sum of water- soluble resin and synthetic resin emulsion to watersoluble photocrosslinking agent is 98: 2 to 70: 30, more preferably 96: 4 to 80: 20. If the water-soluble photo-crosslinking agent is less than this, the sensitivity and the image are lowered remarkably, and inversely, if it is too much, the quality of image is lowered. If coming off seriously said range, the image cannot be obtained. Furthermore, when adding the coloring agents, it is preferable for the colored pigment to be not more than 20 % and for the water-soluble dye to be not more than 10 % to the sum in solids of water-soluble photo-crosslinking agent, water-soluble resin and synthetic resin emulsion. Said components to constitute the photosensitive compositions are prepared by dissolving or dispersing them into water, water/ alcohol mixture, etc.
The photosensitive composition prepared in this way and to be utilized for the image-forming method of the invention is coated onto the supporter to make the positive-positive type image-forming material. As the supporters, plastic films such as poly(ethylene terephthalate), polypropylene, polyethylene, poly(vinyl chloride), polystyrene, polycarbonate, triacetate, etc., glass plate, paper being made water- resistant by laminating with polyethylene, polypropylene or the like on both sides, and the like can be mentioned. Moreover, plastic films provided with the drawing quality such as sand-mat film treated one or both sides by sandblast method to give the writing quality with 8 - pencil, Japanese ink, ball pen, etc., etched mat film submitted to etching with alkali, and others, further opal films kneaded with white pigments, and the like can be used. Moreover, though the photosensitive layer may be coated directly onto said supporter, it is desirable to give beforehand the corona discharge treatment, primer coating or processing for adhesion combined these. As the primers, phenol resin, polyester resin, urethane resin, vinylidene chloride-vinyl acetate copolymer, vinylidene chlorideacrylonitrile copolymer and mixtures of these are used. The film thickness on the supporter is preferable to be 0.1 to 2.0 m.
The coating onto the supporter is performed by arbitrary methods such as coating with rotary coater, roll coating, bar coating, brush coating etc. The coating weight is about 1 to 5 M, preferably about 2 m or so in the film thickness after drying. The thinner the film thickness, the better the resolution of image. After coating, the drying is made usually by hot air of less than about 90 % but this may be airdrying.
According to the imageforming method of the invention, the posicivepositive type imageforming material producedusing said photosensitive composition is treated through following processes. (1) Exposure to light The manuscript is superposed on the coated side with photosensitive composition of image-forming material produced and, to this, the active rays from various mercury-vapor lamps, 1 1 carbon are lamp, xenon lamp, metal halide lamp, UV fluorescent lamp, etc. are irradiated.
(2) Immersion into warm water The image-forming material exposed to light is immersed into warm water to swell and soften the non-image area exposed to light and simultaneously to dissolve out the water-soluble photo-crosslinking agent in the image area not exposed to light into warm water. The temperature of warm water at this time is preferable to be 30 to 60 'C. If using water of lower temperature than 30 % the reproduction of fine lines, small half-tone dots, etc. is difficult because the exposed area does not swell and soften sufficiently. Also, if using water of higher temperature than 60 % the quality of image obtained is lowered or the background contamination of non-image area due to the adhesion of the components of said photosensitive composition to the substrate takes place because the image area is also softened. Furthermore. when using high-temperature water, the environment of operation is worsened due to the vapor thereof. The immersion time int-o warm water is determined by the time to sufficiently swell the non-image area and the time to dissolve out the water-soluble photo-crosslinking agent in the image area into warm water, which necessitates not less than 3 seconds, more preferably not less than 10 seconds. (3) Removal of non-image area and-drying
The photosensitized surface of said imageforming material 1 1 having finished the immersion into warm water is rubbed with sponge, brush, etc. to remove the non-image area. This operation may be carried out under any condition of being in water, in running water, in a vat without water, or the like, using said warm water or normal- temperature water. Then, drying is made.
In following, examples will be shown, but the invention is not confined to these.
Example 1 A liquor (photosensitive liquor) Diazo resin 0.6 parts by wt.
(Condensate of p-diazodiphenylamine with formaldehyde) Denka size PC-100 1.5 parts by wt.
(Copolymer of vinyl alcohol with acrylamide, made by Denkikagaku Kogyo Co., Ltd.) Primal B-15 (46 % liquor) 15.7 parts by wt.
(Emulsion of polyacrylate, made by Nihon Acryl Kagaku Go., Ltd.) Carbon black dispersion Methanol 5.0 parts by wt.
38.6 parts by wt.
-Water 38.6 parts by wt.
However, the carbon black dispersion was obtained by dispersing for 3 hours with ink-mixing mill using a following formulation.
Carbon black 60 parts by wt.
Metholose 60SH 4000 10 parts by wt.
(Hydroxypropylmethyleellulose, made by Shinetsu Kagaku Co., Ltd.) i Nonionic surfactant 1 part by wt.
(Mixture of polyethylenegl.ycol alkylphenyl ether) Water 229 parts by wt.
A liquor was coated onto one side of poly(ethylene terephthalate) film with a thickness of 75 rm by the use of rotary coater and dried by warm air of 90 'C for 90 seconds to form the photosensitive layer with a thickness of 2 p M. Then, a positive manuscript with half -tone dots for printing was closely contacted with the photosensitive layer, which was exposed to light for 10 seconds from a distance of 1 m using 2 KW super high-pressure mercury-vapor lamp. This was immersed into warm water of 45 'C for 60 seconds to sufficiently swell the non-image area. Thereafter, by rubbing the photosensitized surface with sponge to remove the non- image area, a sharp black relief positive image with an optical density of 1.20 was obtained. This image reproduced the half-tone dots of 0.5 - 99.5 % in manuscript. Comparative example 1 The image-forming material being obtained in Example 1 and having finished the exposure to light was immersed into water of 15 'C for 60 seconds and thereafter the photosensitized surface was rubbed with sponge to remove the non-image area. In the positive image thus formed, the half- tone dots of smaller than 20 % in manuscript were found no't to be formed. Comparative example 2 The image-forming material being obtained in Example 1 and having finished the exposure to light was immersed into warm - 12 1 water of 45 'C for 2 seconds and thereafter the photosensitized surface was rubbed with sponge to remove the non-image area. In the positive image thus formed, the halftone dots of smaller than 10 % in manuscript were found not to be formed. Example 2 B liquor (photosensitive liquor) Sodium 4,4'-diazi.dostilbene-2,2'.-disu.1fonate 0.7 parts by wt.
PVP K-90 1.0 part by wt.
(Poly(vinyl-pyrrolidone), made by General Aniline & Film Corp.) Sumielite 1010 (50 % liquor) 10.7 parts by wt.
(Emulsion of ehtylene-vinylchloride copolymer, Sumitomo Kagaku Kogyo Go., Ltd.) Methanol 17.5 parts by wt.
Water 70.1 parts by wt.
Similarly to Example 1, B liquor was coated onto one side of poly(ethylene terephthalate) film with a thickness of 75 m and dried to form the photosensitive layer with 2 um. Then, this was exposed to light for 4 seconds at a distance of 1 m using 2 KW super high- pressure mercury-vapor lamp and immersed into warm water of 40 'C for 10 seconds to sufficiently swell the non-image area. Thereafter, when rubbing lightly the photosensitized layer in running water with sponge allowed to contain water, the non-image area expoed to light was removed to give a colorless positive relief image.
Comparative example 3 13 - The image-forming material being obtained in Example 2 and having finished the exposure to light was immersed into water of 40 'C for 2 seconds and thereafter the photosensitized layer was rubbed lightly in running water with sponge allowed to contain water. At this time, an image close to one obtained in Example 2 was obtained, but the coloring due to the water-soluble photo-crosslinking agent was clearly seen in the image. Example 3 C liquor (photosensitive liquor) 3,3'-Dimethoxydiphenyl-4,4'-bisdiazonium chloride-zinc chloride double salt 1.5 parts by wt.
Polyacrylamide (10 % aqueous solution) 18.0 parts by w-- (Degree of-.polymerization 10000, made by Nakarai Kagaku) Vinybrane 240 (45 % liquor) 8.0 parts by wt.
(Vinyl chloride-based emulsion, made by Nisshin Kagaku Kogyo Co., Ltd.) Carbon black dispersion 6.5 parts by wt.
Methanol 30.0 parts by wt.
Water 36.0 parts by wt.
C liquor was coated onto one side of poly(ethylene terephthalate) film with a thickness of 75 pm by. the use of rotary coater and dried by warm air of 90 C for 60 se conds to form the photosensitive layer with a thickness,of 1.5 p m. Then, a positive manuscript was closely contacte with the photosensitive layer and exposed to light for 12 seconds from a distance of 1 m using 2 KW super high-pressure mercury-vapor.lamp. This was immersed 14 - Z into warm water of 35 'C for 60 seconds to sufficiently swell the non- image area. Thereafter, when rubbing the photosensitized layer with sponge allowed to contain water to remove the nonimage area, a sharp black relief positive image with an optical density of 0.85 was obtained.
Example 4
D liquor (photosensitive liquor) Sodium 4,4'-diazidostilbene-2,2'-disulfonate 0.9 parts by wt.
PVP K-90 0.8 parts by wt.
Sumikaflex 830 (50 % liquor) 16.4 parts by wt.
(Emulsion of vinyl acetate-ethylene-vinylchloride terpolymer, made by Sumitomo Kagaku Kogyo Co., Ltd.) Carbon black dispersion 5.0 parts by wt.
Methanol 38.5 parts by wt.
-Water 38.5 parts by wt.
D liquor was coated onto one side of poly(ethylene terephthalate) film with a thickness of 75 m by the use of rotary coater and dried by warm air of 90 'C for 60 seconds to -form the photosensitive layer with a thickness of 1.5 m. Then, precoat-control wedge UGRA PCW 82 (made by Mika Denshi Co., Ltd.) was closely contacted with the photosensitive layer and exposed to light for 1.2 seconds from a distance of 1 m using 2 KW super highpressure mercury-vapor lamp. This was immersed into warm water of 40 C for 30 seconds to sufficiently swell the non-image area. Thereafter, when rubbing the photosensitized layer in running water with sponge allowed to contain water ot remove the non- 1 4 r image area, a sharp black relief positive image with an optical density of 1.0 was obtained. The image thus formed reproduced fine lines of 6 and half-tone dots of 0.5 - 99.5 Comparative example 4 The image-forming material being obtained in-Example 4 and having finished the exposure to light was immersed into water of 20 'C for 30 seconds and thereafter the photosensitized surface was rubbed in running water with sponge allowed to contain water to remove the non-image area. At this time, image portion with half-tone dots of smaller than 30 % could not be formed.
1

Claims (8)

CLAIMS:-
1. A method of forming a positive-positive type image characterized in that a photosensitive layer is formed on a substrate using a composition comprising a watersoluble photo-crossl inking agent, a water soluble resin and a synthetic resin emulsion and further a colouring agent, if necessary, said photosensitive layer is exposed to active rays through manuscript, then this is immersed into warm water of 30 to WC for not less than 3 seconds to allow -the exposed area to swell and soften sufficiently with warm water and simultaneously to allow substantially all of the water-soluble photo-crosslinking agent in the nonexposed area to dissolve out into warm water, and successively the swollen and softened exposed area is rubbed out to form an image having no colouring originating from water-soluble photo-crossl inking agent without using development chemicals except water.
2. A method according to claim 1, wherein the watersoluble photo-crossl inking agent is an azide compound, a diazonium salt or a tetrazonium salt.
3. A method according to claim 1 or 2 wherein the water-soluble resin is selected from polyacrylamide. poly (vinyl -pyrrol idone) poly(vinyl alcohol), graftpolymerization products of poly(vinyl alcohol) with vinyl monomers, water-soluble poly(vinyl butyral), glue, casein, gelatin, arabic gum, egg albumin, gums, alginic - 17 - acids, poly(ethylene oxide), poly(acrylic acid) and salts thereof, poly(methacrylic acid) and salts thereof, or mixtures of two or more of these, or mixtures of one of more of these with poly(vinyl alcohol) or with a cellulose derivative.
4. A method according to any claims 1 to 3 wherein the synthetic resin emulsions is selected from polyacrylate, ethylene-vinyl acetate copolymer, poly(vinylidene chloride), poly(vinyl acetate), poly(vinyl chloride) copolymers-or mixtures of these.
5. A method according to any of claims 1 to 4, wherein the ratio of solids of water-soluble resin to synthetic resin emulsion is 1:99 to 80:20.
6. A method according to claim 5, wherein the ratio of solids of watersoluble resin to synthetic resin emulsion is 5:95 to 40:60.
7. A method according to any of claims 1 to 6, wherein the ratio of solids of the sum of water-soluble resin and synthetic resin emulsion to water-soluble crosslinking agent is 98:2 to 70:30.
8. A method according to claim 7, wherein the ratio of solids of the sum of water-soluble resin and synthetic resin emulsion to watersoluble crosslinking agent is 96:4 to 80:20.
- is Published 1990 at The Patent Mice. State House.6671 High Holborn.London WC1R 4TP. Further copies maybe obtainedfrom The Patent Oilice Wes Branch. St Mary Cray. Orphigton. Kent BRS 3RD. Printed by MWuplex techniques ltd. St Mary Cray, Kent, Con. V87 1 1
GB8905742A 1988-01-12 1989-03-13 Method of forming reversal images Expired - Fee Related GB2229286B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP460788A JPH01180540A (en) 1988-01-12 1988-01-12 Image forming method

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GB8905742D0 GB8905742D0 (en) 1989-04-26
GB2229286A true GB2229286A (en) 1990-09-19
GB2229286B GB2229286B (en) 1993-04-07

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DE (1) DE3908506A1 (en)
FR (1) FR2644907A1 (en)
GB (1) GB2229286B (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04369651A (en) * 1991-06-18 1992-12-22 Sanyo Kokusaku Pulp Co Ltd Multicolor image forming method
JP2596271B2 (en) * 1991-09-10 1997-04-02 双葉電子工業株式会社 Method for producing photosensitive composition and substrate
AT404095B (en) * 1993-12-10 1998-08-25 Petritsch Erich CLEANING AND CARE PRODUCTS FOR HUMAN HAIR AND METHOD FOR THE PRODUCTION THEREOF
EP0749080B1 (en) * 1995-06-16 2000-09-13 Seiko Epson Corporation Order management system

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DE2522225C2 (en) * 1975-05-20 1983-12-08 Nippon Paint Co., Ltd., Osaka Aqueous photosensitive mixture and its use for the production of screen printing stencils
DE2834059A1 (en) * 1978-08-03 1980-02-14 Hoechst Ag LIGHT SENSITIVE COPY MATERIAL AND METHOD FOR THE PRODUCTION THEREOF
JPS5965840A (en) * 1982-10-07 1984-04-14 Sanyo Kokusaku Pulp Co Ltd Formation of colored image and photosensitive material for forming colored image
JPS59166945A (en) * 1982-10-25 1984-09-20 Nippon Kankoushi Kogyo Kk Water-developable photosensitive sheet having high light shielding property
JPS60133440A (en) * 1983-12-22 1985-07-16 Sanyo Kokusaku Pulp Co Ltd Image forming material and image forming method
JPH0693118B2 (en) * 1987-06-15 1994-11-16 日本製紙株式会社 Photosensitive sheet

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JPH01180540A (en) 1989-07-18
FR2644907A1 (en) 1990-09-28
GB2229286B (en) 1993-04-07
DE3908506A1 (en) 1990-09-20
JPH0551897B2 (en) 1993-08-03
GB8905742D0 (en) 1989-04-26

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732E Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977)
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Effective date: 19970313