GB1221325A - Dormation of dye images from photographic images - Google Patents
Dormation of dye images from photographic imagesInfo
- Publication number
- GB1221325A GB1221325A GB06629/68A GB1662968A GB1221325A GB 1221325 A GB1221325 A GB 1221325A GB 06629/68 A GB06629/68 A GB 06629/68A GB 1662968 A GB1662968 A GB 1662968A GB 1221325 A GB1221325 A GB 1221325A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dye
- acid
- image
- vinyl
- monomer
- 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.)
- Expired
Links
- 239000000178 monomer Substances 0.000 abstract 8
- 239000000975 dye Substances 0.000 abstract 7
- 229910052709 silver Inorganic materials 0.000 abstract 6
- 239000004332 silver Substances 0.000 abstract 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract 4
- -1 silver halide Chemical class 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 239000003638 chemical reducing agent Substances 0.000 abstract 3
- 239000000839 emulsion Substances 0.000 abstract 3
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 2
- 238000004043 dyeing Methods 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- 238000005406 washing Methods 0.000 abstract 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical class C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 abstract 1
- 229940018563 3-aminophenol Drugs 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- 239000000980 acid dye Substances 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 125000003368 amide group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 239000000981 basic dye Substances 0.000 abstract 1
- 239000007853 buffer solution Substances 0.000 abstract 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 abstract 1
- 239000011976 maleic acid Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
- G03F7/0285—Silver salts, e.g. a latent silver salt image
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
1,221,325. Photo-polymerization process for the production of dye images. FUJI SHASHIN FILM K.K. April 5, 1968 [April 6, 1967J, No.16629/68. Heading G2C. Dye images are produced by imagewise exposing a negative or positive silver halide emulsion to electromagnetic waves or particle rays, contacting the exposed emulsion with a reducing agent which is resorcinol or m-aminophenol or a derivative of either or a naphthol containing either two hydroxyl groups or one hydroxyl group and one amino group or one amido group in the 1, 6; 1, 8 or 2, 7 positions, and with a vinyl or vinylidene monomer or a maleate containing an acid or basic group thus polymerizing the monomer in the areas corresponding to the latent silver image and dyeing with a dye having an acidity or basicity opposite to that of the polymer. The silver image which is produced on polymerization may be bleached out before or after dyeing the polymer image. The dye image may be transferred to a receptor sheet by the conventional spirit duplicating process. Specified monomers with acid groups are acrylic, methacrylic and maleic acid and their ammonium, alkali metal and alkaline earth salts and vinyl sulphonic acid and its ammonium and alkali metal salts. Specified monomers with basic groups are vinyl pyridines, N, N-dialkylaminoethyl-acrylates and -methacrylates and vinyl monomers containing quaternary ammonium salts. Monomers which do not contain such groups may be added to the monomer mixture. In the examples, various negative and positive silver halide emulsions are imagewise exposed and contacted with a solution containing alkali, reducing agent and monomer. The silver image is then fixed and the material immersed in the appropriate dye and acid (if a basic dye is used) or a buffer solution ofpH 5À0 (if an acid dye is used). The silver image may be removed by Farmer's reducer and the dye image remaining may be transferred to a receptor sheet. The processing solution preferably contains a sulphite ion. Any dye in the unpolymerized areas is removed by washing with acetic acid or the unpolymerized areas may be removed by washing.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2200267 | 1967-04-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1221325A true GB1221325A (en) | 1971-02-03 |
Family
ID=12070783
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB06629/68A Expired GB1221325A (en) | 1967-04-06 | 1968-04-05 | Dormation of dye images from photographic images |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3756818A (en) |
| BE (1) | BE713299A (en) |
| FR (1) | FR1574759A (en) |
| GB (1) | GB1221325A (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4131466A (en) * | 1972-03-05 | 1978-12-26 | Somar Manufacturing Co., Ltd. | Photographic method of making relief member with negative dye image |
| US4391894A (en) * | 1974-11-06 | 1983-07-05 | Polychrome Corporation | Colored photosensitive composition |
| FR2406230A1 (en) * | 1977-10-11 | 1979-05-11 | Eastman Kodak Co | PHOTOSENSITIVE AND PRODUCED COMPOSITION |
| JPS57172336A (en) | 1981-04-17 | 1982-10-23 | Fuji Photo Film Co Ltd | Black-and-white photosensitive material |
| US5032486A (en) * | 1990-03-02 | 1991-07-16 | Minnesota Mining And Manufacturing Company | Method for forming printing plates and plate-making element |
| BR9803596A (en) * | 1997-09-23 | 2000-04-25 | Pfizer Prod Inc | Derivatives of resorcinol. |
| US6878381B2 (en) * | 1999-03-22 | 2005-04-12 | Pfizer, Inc | Resorcinol composition |
| US6828460B2 (en) * | 1999-03-22 | 2004-12-07 | Pfizer Inc. | Resorcinol derivatives |
| JP2011093308A (en) * | 2009-09-30 | 2011-05-12 | Fujifilm Corp | Resin composition for laser engraving, relief printing plate precursor for laser engraving and method for producing the same, and relief printing plate and method for making the same |
-
1968
- 1968-04-05 BE BE713299D patent/BE713299A/xx unknown
- 1968-04-05 FR FR1574759D patent/FR1574759A/fr not_active Expired
- 1968-04-05 GB GB06629/68A patent/GB1221325A/en not_active Expired
-
1971
- 1971-04-30 US US00139131A patent/US3756818A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| FR1574759A (en) | 1969-07-18 |
| DE1772146A1 (en) | 1975-06-19 |
| BE713299A (en) | 1968-08-16 |
| DE1772146B2 (en) | 1976-12-09 |
| US3756818A (en) | 1973-09-04 |
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