GB537081A - Improvements in or relating to light-sensitive photographic materials - Google Patents
Improvements in or relating to light-sensitive photographic materialsInfo
- Publication number
- GB537081A GB537081A GB31648/39A GB3164839A GB537081A GB 537081 A GB537081 A GB 537081A GB 31648/39 A GB31648/39 A GB 31648/39A GB 3164839 A GB3164839 A GB 3164839A GB 537081 A GB537081 A GB 537081A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- layer
- soluble
- acetic acid
- per cent
- 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
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
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/825—Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
- G03C1/835—Macromolecular substances therefor, e.g. mordants
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Laminated Bodies (AREA)
Abstract
537,081. Photographic anti-helation layers. DU PONT FILM MANUFACTURING CORPORATION. Dec. 6, 1939, No. 31648. Convention date, Dec. 13, 1938. [Class 98 (ii)] Light-sensitive photographic material comprises a transparent support carrying a lightsensitive layer on one side and an anti-halation layer on the other side comprising an antihalation dye or pigment and a polymeric nitrogen compound which contains one or more amino groups and which is insoluble in water and 5 per cent. ammonium hydroxide solution but which is soluble in 5 per cent. aqueous acetic acid, preferably in 2 to 5 per cent. aqueous acetic acid. The light-sensitive layer may be a panchromatic or orthochromatic emulsion layer. The nitrogen compound may be deacetylated chitin ; an acid-soluble reaction product of a protein with a carboxyl compound such as a lower aliphatic aldehyde or ketone and an amine having less than nine carbon atoms in which the amino-nitrogen is joined to the aliphatic carbon; an amino cellulose soluble in dilute acetic acid and containing an amino-nitrogen atom removed from the cellulose nucleus by at least one carbon atom; cellulose amines soluble in a stoichiometrical amount of 5 per cent. acetic acid and containing directly attached to the cellulose nucleus from 0.5 to 1.5 amino nitrogens per glucose unit; the reaction products of vinyl ketone polymers with amino compounds ; the products obtained by treating resins having ketone groups with excess ammonia or amines and catalytically hydrogenating; polymeric amino alcohol esters of acrylic and substituted acrylic acids ; and polymeric alcohol methacrylates. The compounds may be used singly or in admixture. Resinous reaction products of phenols, aldehydes and ammonia or primary or secondary amines may be used, for example the reaction product of m-cresol, formaldehyde, and dimethylamine. Examples specified are piperidylmethylzein, dimethylaminomethylzein, dimethylaminoethylzein, and dicyclohexyl aminoethyl methacrylate. The dyes may be water-or spirit-soluble and may be blue, green, yellow, magenta, or red, or may be used in combination to give black or deep blue. Black or red antihalation layers are used with blue-sensitive or orthochromatic emulsions, and black, green or deep blue with panchromatic emulsions. Numerous dyes are specified. Naturally occurring pigments, metallo-dye complexes, and inorganic coloured compounds may be used. The layer may be applied by dipping, transfer, spraying, beading, or immersion beading. The antihalation layer may be rendered soluble before fixing by treatment in an acetic or citric acid bath, such as a stop bath. The emulsion layer may contain sensitizers such as cyanines, carbocyanines, pseudocyanines or cyazine bases or salts. The antihalation layer may be permanent, the dye concentration being reduced and alum added to the coating solution. Specifications 475,131 and 475,132, [both in Group IV], are referred to. Reference has been directed by the Comptroller to Specification 517,559.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US245528A US2182794A (en) | 1938-12-13 | 1938-12-13 | Photographic elements containing antihalation layers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB537081A true GB537081A (en) | 1941-06-09 |
Family
ID=22927040
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31648/39A Expired GB537081A (en) | 1938-12-13 | 1939-12-06 | Improvements in or relating to light-sensitive photographic materials |
Country Status (2)
Country | Link |
---|---|
US (1) | US2182794A (en) |
GB (1) | GB537081A (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2527262A (en) * | 1944-10-30 | 1950-10-24 | Ilford Ltd | Photographic layers containing gelatin-anion soap complexes and their preparation |
US2448542A (en) * | 1946-08-01 | 1948-09-07 | Du Pont | Photographic elements having antihalation layers composed of vinylpyridine polymers and antihalation materials |
US2448507A (en) * | 1946-08-01 | 1948-09-07 | Du Pont | Photographic elements having antihalation layer composed of vinylpyridine polymer with vinylpyridine polymer sublayer and outer protective layer |
US3075841A (en) * | 1956-06-19 | 1963-01-29 | Du Pont | Mordant treating process and elements containing same |
US3087815A (en) * | 1959-04-22 | 1963-04-30 | Polaroid Corp | Photographic diffusion transfer process |
BE677997A (en) * | 1965-03-29 | 1966-09-01 | ||
US4258119A (en) * | 1979-12-26 | 1981-03-24 | Polaroid Corporation | Novel xanthene compounds and photographic products and processes employing the same |
US4310673A (en) * | 1979-12-26 | 1982-01-12 | Polaroid Corporation | Xanthene compounds |
US4304834A (en) * | 1979-12-26 | 1981-12-08 | Polaroid Corporation | Novel xanthene compounds and photographic products and processes employing the same |
US4290950A (en) * | 1979-12-26 | 1981-09-22 | Polaroid Corporation | Sulfo-substituted-3,6-di(N-indolinyl)-9-sulfonamidophenyl-xanthenes |
US4258118A (en) * | 1979-12-26 | 1981-03-24 | Polaroid Corporation | Novel xanthene compounds and photographic products and processes employing the same |
US4311847A (en) * | 1979-12-26 | 1982-01-19 | Polaroid Corporation | Xanthene compounds |
US4290951A (en) * | 1979-12-26 | 1981-09-22 | Polaroid Corporation | 3,6-Di(N-indolinyl)-9-sulfonamidophenyl-xanthenes |
US4290955A (en) * | 1979-12-26 | 1981-09-22 | Polaroid Corporation | 3,6-Di(alkyl/phenyl)amino-9-carboxamidophenyl-xanthenes |
US4316950A (en) * | 1979-12-26 | 1982-02-23 | Polaroid Corporation | Novel xanthene compounds and photographic products and processes employing the same |
US4345017A (en) * | 1980-10-06 | 1982-08-17 | Polaroid Corporation | Photographic products and processes with a pH sensitive xanthene light screening dye |
US4416971A (en) * | 1982-12-28 | 1983-11-22 | Polaroid Corporation | Novel xanthene compounds and their photographic use |
US5187282A (en) * | 1991-04-08 | 1993-02-16 | Polaroid Corporation | Sulfonated xanthene dyes, and photographic products and processes employing these dyes |
US5264322A (en) * | 1991-04-08 | 1993-11-23 | Polaroid Corporation | Sulfonated xanthene dyes, and photographic products and processes employing these dyes |
-
1938
- 1938-12-13 US US245528A patent/US2182794A/en not_active Expired - Lifetime
-
1939
- 1939-12-06 GB GB31648/39A patent/GB537081A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US2182794A (en) | 1939-12-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB537081A (en) | Improvements in or relating to light-sensitive photographic materials | |
US2397452A (en) | Photographic element | |
US2100063A (en) | Process for the production of tanned pictures | |
US2182814A (en) | Photographic film | |
US3271148A (en) | Mordanting of acid dyes | |
JPS5950973B2 (en) | Photosensitive photographic materials containing light-absorbing dyes | |
US2328034A (en) | Photographic element and process | |
US2197809A (en) | Photographic process and emulsion utilizing cation-active surface active agents | |
US3269840A (en) | Method and material for surface brightening layers containing gelatin as the binding agent using anionic water-soluble diaminostilbene fluorescent compounds | |
US2363764A (en) | Color photography | |
US1760780A (en) | Light-sensitive layers and process of preparing them | |
US2386167A (en) | Photographic article of manufacture | |
US3795519A (en) | Photographic materials containing mordants | |
US2323481A (en) | Chemical process and composition | |
US2066918A (en) | Light-sensitive material and a proc | |
US2500111A (en) | Azanol dyes | |
US2369171A (en) | Methods of photography | |
US2282890A (en) | Antihalo coating for photographic material | |
US3512983A (en) | Photographic light-sensitive materials containing mordanted oxonol dyes | |
US2461485A (en) | Xanthylium dye salts as filter and antihalation dyes in photographic materials | |
US2534050A (en) | Process of treating photographic layers containing color formers with metal salt hardening agents | |
US2572988A (en) | Production of colored colloid layers | |
US2396275A (en) | Processes of color photography and compositions and elements therefor utilizing polymeric quaternary ammonium dye intermediates | |
DE849651C (en) | Dyes for antihalation layers | |
US2635536A (en) | Mordanting |