GB1148483A - Dispersions of physical development nuclei - Google Patents
Dispersions of physical development nucleiInfo
- Publication number
- GB1148483A GB1148483A GB35567/68A GB3556768A GB1148483A GB 1148483 A GB1148483 A GB 1148483A GB 35567/68 A GB35567/68 A GB 35567/68A GB 3556768 A GB3556768 A GB 3556768A GB 1148483 A GB1148483 A GB 1148483A
- Authority
- GB
- United Kingdom
- Prior art keywords
- units
- formula
- atoms
- alkyl
- april
- 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
- 239000006185 dispersion Substances 0.000 title abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 239000001828 Gelatine Substances 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 229920000159 gelatin Polymers 0.000 abstract 2
- 235000019322 gelatine Nutrition 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- -1 α-amylose Chemical class 0.000 abstract 2
- 229920000856 Amylose Polymers 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 229920002301 cellulose acetate Polymers 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 238000009792 diffusion process Methods 0.000 abstract 1
- 150000004676 glycans Chemical class 0.000 abstract 1
- 229920001519 homopolymer Polymers 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 229920001282 polysaccharide Polymers 0.000 abstract 1
- 239000005017 polysaccharide Substances 0.000 abstract 1
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/04—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of inorganic or organo-metallic compounds derived from photosensitive noble metals
- G03C8/06—Silver salt diffusion transfer
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/44—Preparation of metal salts or ammonium salts
-
- 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
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/04—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
- G03C1/053—Polymers obtained by reactions involving only carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
-
- 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
-
- 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/24—Photosensitive materials characterised by the image-receiving section
- G03C8/26—Image-receiving layers
- G03C8/28—Image-receiving layers containing development nuclei or compounds forming such nuclei
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/10—Copolymer characterised by the proportions of the comonomers expressed as molar percentages
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/923—Ethylenic monomers containing at least one salt group
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Physics & Mathematics (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
1,148,483. Photographic dispersions. EASTMAN KODAK CO. April 15, 1966 [April 15, 1965], No.35567/68. Divided out of 1,148,482. Heading G2C. An aqueous dispersion of physical development nuclei has a peptising agent for the nuclei comprising a homopolymer of units of formula 1 or 2 (as defined below), or a copolymer of units of formula 1 or 2 and units of formula 3 in which the ratio of the total number of units to the number of units of formula 1 or 2 is not above 5:1. Formulae 1 and 2 are and formula 3 is wherein # is the repeating unit of a hydrophillic polysaccharide, e.g. α-amylose, or a hydrolyzed cellulose acetate; R 1 and R 2 are each alkyl of 1-8 C atoms, or aryl, or together form a heterocyctic ring which may contain further N, O or S atoms; R 3 is alkyl of 1-6 C atoms; and B and D are each H, OH, alkyl, aryl, acyl, acyloxy, cyano, diacylimido, alkyloxy, aryloxy, carbonyl or carboxy. The dispersion may be coated to form imagereceiving layers for the silver salt diffusion process, and may also contain gelatine in a gelatine: polymer ratio of 99À1. The polymers also have a black-toning effect on the transferred image.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US44826665A | 1965-04-15 | 1965-04-15 | |
US448264A US3345346A (en) | 1965-04-15 | 1965-04-15 | Aminopolymer compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1148483A true GB1148483A (en) | 1969-04-10 |
Family
ID=27035291
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16509/66A Expired GB1148482A (en) | 1965-04-15 | 1966-04-15 | Silver halide dispersions |
GB35567/68A Expired GB1148483A (en) | 1965-04-15 | 1966-04-15 | Dispersions of physical development nuclei |
GB16510/66A Expired GB1139446A (en) | 1965-04-15 | 1966-04-15 | Polymers containing n,n-disubstituted vinyloxymethylamine units |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16509/66A Expired GB1148482A (en) | 1965-04-15 | 1966-04-15 | Silver halide dispersions |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16510/66A Expired GB1139446A (en) | 1965-04-15 | 1966-04-15 | Polymers containing n,n-disubstituted vinyloxymethylamine units |
Country Status (4)
Country | Link |
---|---|
US (1) | US3425836A (en) |
BE (1) | BE678582A (en) |
DE (2) | DE1595569B2 (en) |
GB (3) | GB1148482A (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3637394A (en) * | 1968-04-22 | 1972-01-25 | Eastman Kodak Co | Photographic elements containing synthetic polymeric vehicles |
US3816129A (en) * | 1973-01-02 | 1974-06-11 | Polaroid Corp | Synthetic silver halide emulsion binder |
US3962527A (en) * | 1973-03-09 | 1976-06-08 | Eastman Kodak Company | Novel polymers and photographic elements containing same |
US4299898A (en) * | 1979-05-03 | 1981-11-10 | Xerox Corporation | Positively charged toners containing quaternary ammonium salts attached to acrylate polymers |
US5804363A (en) * | 1997-04-28 | 1998-09-08 | Eastman Kodak Company | High bromide (111) tabular grain emulsions containing a cationic peptizer having diallylammonium derived repeating units |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2358836A (en) * | 1942-05-26 | 1944-09-26 | Eastman Kodak Co | Water-soluble polyvinyl acetals |
US2725381A (en) * | 1953-02-02 | 1955-11-29 | Eastman Kodak Co | Process of preparing methyl 4-vinylpyridinium p-toluenesulfonate |
BE542633A (en) * | 1954-11-08 |
-
1965
- 1965-04-15 US US448266A patent/US3425836A/en not_active Expired - Lifetime
-
1966
- 1966-03-10 DE DE19661595569 patent/DE1595569B2/en active Pending
- 1966-03-28 BE BE678582D patent/BE678582A/xx unknown
- 1966-04-13 DE DE19661547678 patent/DE1547678A1/en active Pending
- 1966-04-15 GB GB16509/66A patent/GB1148482A/en not_active Expired
- 1966-04-15 GB GB35567/68A patent/GB1148483A/en not_active Expired
- 1966-04-15 GB GB16510/66A patent/GB1139446A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE1595569B2 (en) | 1971-04-08 |
BE678582A (en) | 1966-09-01 |
US3425836A (en) | 1969-02-04 |
GB1148482A (en) | 1969-04-10 |
DE1595569A1 (en) | 1970-03-19 |
GB1139446A (en) | 1969-01-08 |
DE1547678A1 (en) | 1971-11-25 |
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