GB522611A - Photographic multilayer material - Google Patents
Photographic multilayer materialInfo
- Publication number
- GB522611A GB522611A GB36170/38A GB3617038A GB522611A GB 522611 A GB522611 A GB 522611A GB 36170/38 A GB36170/38 A GB 36170/38A GB 3617038 A GB3617038 A GB 3617038A GB 522611 A GB522611 A GB 522611A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- dye
- prepared
- destruction
- catalyst
- 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
- 239000000463 material Substances 0.000 title abstract 4
- 239000000839 emulsion Substances 0.000 abstract 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 8
- 239000003054 catalyst Substances 0.000 abstract 7
- 239000000975 dye Substances 0.000 abstract 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 6
- 239000002253 acid Substances 0.000 abstract 5
- 239000007859 condensation product Substances 0.000 abstract 4
- 229910052709 silver Inorganic materials 0.000 abstract 4
- 239000004332 silver Substances 0.000 abstract 4
- -1 silver halide Chemical class 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 238000009835 boiling Methods 0.000 abstract 3
- 230000006378 damage Effects 0.000 abstract 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 abstract 3
- HTZQXEMZXPWJDX-UHFFFAOYSA-N 3-amino-2-hydroxyphenazine-1-sulfonic acid Chemical compound OC1=C(C2=NC3=CC=CC=C3N=C2C=C1N)S(=O)(=O)O HTZQXEMZXPWJDX-UHFFFAOYSA-N 0.000 abstract 2
- SIXYIEWSUKAOEN-UHFFFAOYSA-N 3-aminobenzaldehyde Chemical compound NC1=CC=CC(C=O)=C1 SIXYIEWSUKAOEN-UHFFFAOYSA-N 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- GHFIQVSGTXNJBU-UHFFFAOYSA-N CC1=C2N=C(C(=NC2=CC=C1)C(=O)NC1=CC=CC=C1)C Chemical compound CC1=C2N=C(C(=NC2=CC=C1)C(=O)NC1=CC=CC=C1)C GHFIQVSGTXNJBU-UHFFFAOYSA-N 0.000 abstract 2
- 239000011230 binding agent Substances 0.000 abstract 2
- 238000009833 condensation Methods 0.000 abstract 2
- 230000005494 condensation Effects 0.000 abstract 2
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 abstract 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 abstract 1
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 abstract 1
- IUUPZPPZGSLUCK-UHFFFAOYSA-N 3,10-diazapentacyclo[12.8.0.02,11.04,9.015,20]docosa-1(14),2,4,6,8,10,12,15(20),16,18,21-undecaene-18-carboxylic acid Chemical compound C1=C2C=CC3=C(C=CC=4N=C5C=CC=CC5=NC34)C2=CC=C1C(=O)O IUUPZPPZGSLUCK-UHFFFAOYSA-N 0.000 abstract 1
- QAQPSNISVGXVPO-UHFFFAOYSA-N 3,10-diazapentacyclo[12.8.0.02,11.04,9.015,20]docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene Chemical compound C1=C2C=CC3=C(C=CC=4N=C5C=CC=CC5=NC34)C2=CC=C1 QAQPSNISVGXVPO-UHFFFAOYSA-N 0.000 abstract 1
- AJIRUIWLEVHQMU-UHFFFAOYSA-N 3-aminophenazin-2-ol Chemical compound C1=CC=C2N=C(C=C(C(N)=C3)O)C3=NC2=C1 AJIRUIWLEVHQMU-UHFFFAOYSA-N 0.000 abstract 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 abstract 1
- 108010010803 Gelatin Proteins 0.000 abstract 1
- SFKCYHZUZURQLB-UHFFFAOYSA-N N-(3-aminophenazin-2-yl)octadecanamide Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)NC1=CC2=NC3=CC=CC=C3N=C2C=C1N SFKCYHZUZURQLB-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract 1
- 229960000583 acetic acid Drugs 0.000 abstract 1
- 239000000987 azo dye Substances 0.000 abstract 1
- 238000004061 bleaching Methods 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000000084 colloidal system Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 abstract 1
- 229920000159 gelatin Polymers 0.000 abstract 1
- 239000008273 gelatin Substances 0.000 abstract 1
- 235000019322 gelatine Nutrition 0.000 abstract 1
- 235000011852 gelatine desserts Nutrition 0.000 abstract 1
- 239000012362 glacial acetic acid Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 238000010348 incorporation Methods 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000002244 precipitate Substances 0.000 abstract 1
- 230000001376 precipitating effect Effects 0.000 abstract 1
- 238000001556 precipitation Methods 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 230000002829 reductive effect Effects 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 238000006467 substitution reaction Methods 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/28—Silver dye bleach processes; Materials therefor; Preparing or processing such materials
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE437332D BE437332A (en:Method) | 1938-12-12 | ||
| GB36170/38A GB522611A (en) | 1938-12-12 | 1938-12-12 | Photographic multilayer material |
| US253229A US2183395A (en) | 1938-12-12 | 1939-01-27 | Light-sensitive material for producing photographic dye images |
| FR862223D FR862223A (fr) | 1938-12-12 | 1939-12-12 | Produit pour l'obtention d'images photographiques en couleurs |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB36170/38A GB522611A (en) | 1938-12-12 | 1938-12-12 | Photographic multilayer material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB522611A true GB522611A (en) | 1940-06-21 |
Family
ID=10385621
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB36170/38A Expired GB522611A (en) | 1938-12-12 | 1938-12-12 | Photographic multilayer material |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2183395A (en:Method) |
| BE (1) | BE437332A (en:Method) |
| FR (1) | FR862223A (en:Method) |
| GB (1) | GB522611A (en:Method) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE488117A (en:Method) * | 1948-03-27 | |||
| BE579274A (en:Method) * | 1958-06-03 | |||
| NL286940A (en:Method) * | 1961-12-20 | |||
| CH433980A (de) * | 1964-07-07 | 1967-04-15 | Ciba Geigy | Verwendung von Acylaminoverbindungen als Farbbleichkatalysatoren für das Silberfarbbleichverfahren |
| CH450163A (de) * | 1965-03-02 | 1968-01-15 | Ciba Geigy | Photographisches Material für das Silberfarbbleichverfahren |
| US3498787A (en) * | 1965-08-20 | 1970-03-03 | Eastman Kodak Co | Rapid dye-bleach photographic process and element comprising dye-developers |
| US3457074A (en) * | 1966-04-22 | 1969-07-22 | Eastman Kodak Co | Silver dye bleach element containing ballasted para-quinone as diffusion inhibitor |
| CH596580A5 (en:Method) * | 1974-10-28 | 1978-03-15 | Ciba Geigy Ag |
-
0
- BE BE437332D patent/BE437332A/xx unknown
-
1938
- 1938-12-12 GB GB36170/38A patent/GB522611A/en not_active Expired
-
1939
- 1939-01-27 US US253229A patent/US2183395A/en not_active Expired - Lifetime
- 1939-12-12 FR FR862223D patent/FR862223A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR862223A (fr) | 1941-03-01 |
| BE437332A (en:Method) | |
| US2183395A (en) | 1939-12-12 |
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