US2857274A - Photographic compositions and processes - Google Patents
Photographic compositions and processes Download PDFInfo
- Publication number
- US2857274A US2857274A US378684A US37868453A US2857274A US 2857274 A US2857274 A US 2857274A US 378684 A US378684 A US 378684A US 37868453 A US37868453 A US 37868453A US 2857274 A US2857274 A US 2857274A
- Authority
- US
- United States
- Prior art keywords
- atoms
- silver halide
- silver
- photographic
- image
- 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 - Lifetime
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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
- G03C8/08—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds
- G03C8/10—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors
- G03C8/12—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors characterised by the releasing mechanism
- G03C8/14—Oxidation of the chromogenic substances
- G03C8/16—Oxidation of the chromogenic substances initially diffusible in alkaline environment
-
- 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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/38—Fixing; Developing-fixing; Hardening-fixing
Definitions
- the present invention relates to photography and more particularly to photographic compositions, processes and products.
- Photographic processing compositions capable of forming water-soluble, complex silver salts are known to be useful in many phases of silver halide photography.
- a photographic composition which includes a silver halide developer as well as a silver complexing agent is useful in processing a silver halide element by reducing its exposed silver halide to silver, by reacting with its unreduced silver halide to form a water-soluble, complex silver salt and by transferring the salt to an image-receptive element, there to form a visible image.
- the silver complexing agents of the prior art have various shortcomings with respect to transfer processes of this type. For example: certain complexing agents, e. g., ammonia, are too weak to be effective in the production of transfer images; others, e. g., sodium thiosulfate, leave on the transfer image a harmful sulfur residue; and still others, e. g., sodium cyanide, are often impractical because of their dangerous toxicity.
- Objects of the present invention are to provide compositions, processes and products related to a novel association of complexing agents which together are unusually adapted to react with silver halide to form water-soluble silver salts.
- the invention accordingly comprises the several steps and the relation and order of one or more such steps with respect to each of the others, and the composition and product possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.
- the present invention is predicated upon the discovery that soluble, complex silver salts, useful, for example, in the production of transfer images, may be formed by reacting silver halide, in alkaline aqueous solution, with two associated 'complexing agents, the first of which is a cyclic imide and the second of which is a nitrogenous base. It has been found unexpectedly that two such associated complexing agents, together, are more effective in the production of transfer images than is either,
- Preferred cyclic imides to be employed, in accordance with the present invention are characterized by the following general formula:
- Z represents (1) atoms of a series completing 'succinimides, maleimides,
- a cyclic imide nucleus consisting of from 5 to 6 atoms of which from 1 to 3 are nitrogen and the remainder are carbon and (2) members branching from the atoms of the series, at least one of the members being selected from the class consisting of hydrogen atoms, amino radicals and aliphatic radicals containing from 1 to 4 carbon atoms, at most one of the members being selected from the class consisting of halogen atoms, keto oxygen atoms and aromatic radicals.
- Typical preferred cyclic imides are triazines, barbiturates, uracils, urazoles, hydantoins, glutarimides, glutaconimides, and quaternary ammonium salts, examples of which follow:
- Typical preferred nitrogenous bases are:
- bases which are capable of imparting an appropriate alkalinity to the composition; mention may be made of alkali-metal hydroxides such as sodium and potassium hydroxide and amines such as diethylamine and allylamine.
- alkali-metal hydroxides such as sodium and potassium hydroxide
- amines such as diethylamine and allylamine.
- diethylamine can perform, at once, both this function and a complexing function.
- a composition embodying the present invention is broadly useful in a variety of photographic processes of the type in which water-soluble silver complexes are formed from the unreduced silver halide of a photoexposed and at least partially developed silver halide element.
- a composition embodying the present invention specifically suitable for use in the production of transfer images comprises, in addition to associated complexing agents of the above-described type, a suitable silver halide developer, preferably organic, such as hydroquinone, chlorohydroquinone, bromohydroquinone, dichlorohydroquinone, toluhydroquinone, metol, glycin, p-aminophenol hydrochloride, pyrocatechin, pyrogallol and ascorbic acid.
- a nitrogenous base as p-aminophenol can perform, at once, both a developing function and a complexing function.
- the composition is spread in a uniformly thin layer between the superposed surfaces of a photoexposed gelatino silver halide element and an image-receptive element, for example, by advancing the elements between a pair of pressure-applying rollers.
- the elements are maintained in superposed relation for a predetermined period, preferably of the order of 40 to 120 seconds in duration, during which exposed silver halide is reduced to silver and unreduced silver halide forms a water-soluble, complex salt which diffuses through the layer of composition to the image-receptive element, there to be reduced to silver and to form a visible print.
- the silver halide element is stripped from the image-receptive element.
- the image-receptive element preferably, includes certain materials the presence of which, during the transfer process, has a desirable effect on the amount and character of silver precipitated on the image-receptive element.
- Materials of this type are specifically described in copending U. S. patent applications Serial No. 727,385, filed by Edwin H. Land on February 8, 1947, for Photographic Product and Process and Serial No. 164,908, filed by Edwin H. Land on May 29, 1950, for Fhotographic Silver Halide Product and Process.
- a composition employed in the foregoing manner preferably is relatively viscous, of the order of 100 to 200,000 centipoises at a temperature of 20 C., so as to be easily controlled when spread.
- the viscosity of the composition can be increased by including within it a suitable thickening agent, such, for example, as a watersoluble synthetic polymer, an insoluble, emulsifiable oil, a starch, or a gum. It is possible that such a nitrogenous base as polyethylene imine performs, at once, both a thickening function and a complexing function.
- a composition of the present invention within a hermetically sealed container which is ruptured and discharges its contents upon advancing between a pair of pressure-applying rollers of the foregoing type.
- a container for example, may be constructed from a bank of three-ply sheet material having a single fold.
- the outer ply serves as a backing or support and is composed of a thin, relatively inexpensive, tough material, preferably a paper such as kraft paper.
- the intermediate ply is composed of a substantially vapor-, liquid-impervious material, for example a metal foil such as lead foil.
- the inner ply is composed of a thermoplastic or thermosetting plastic material, for example a polyvinyl acetal such as polyvinyl butyral or polyvinyl formal which protects the container contents from contamination.
- a composition comprising by weight approximately 60% to 70% polyvinyl butyral,
- each container the two folds of the inner ply are sealed to each other as by the application of heat and pressure.
- Those two sections of the two folds defining the mouth are bonded together by a strip of adhesive which is so constituted that the adhesive forces between the strip and the inner ply are less than the cohesive forces between end portions of the inner ply which are sealed together.
- a satisfactory strip may be composed, for example, of ethyl cellulose or a mixture of ethyl cellulose and paraffin, the mixture including at least 50% by weight of ethyl cellulose. Since the bonding forces between those sections defining the mouth are less than the bonding forces between other sections of the container, the application of opposed compressional forces to the container causes discharge of the container contents through its mouth.
- Stripping of the silver halide element from the imagereceptive element may separate the layer of processing composition from the image-receptive element or may permit the layer of processing composition to remain in contact with the image-receptive element in order to form a protective coating.
- Techniques which enable such stripping to be accomplished as desired are taught in copending U. S. Patent No. 2,647,056, issued to Edwin H. Land on l'uly 28, 1953, for One Step Photographic Transfer Process. Where the processing composition employs a volatile nitrogenous base, i.
- the reaction product residue of the composition and silver halide will remain substantially colorless when present on the silver image either as a trace remaining after the processing composition layer has been separated from the silver image or within the protective coating formed when the processing composition has been permitted to remain upon the silver image.
- compositions, embodying the present invention which are suitable for use in transfer processes of the foregoing type:
- Example 1 Water cc 400 .
- Example 2 The formula of Example 1 except that the aminoethyl ethanol amine is replaced by an equal quantity of triethylene tetramine.
- Example 3 The formula of Example 1 except that the aminoethyl ethanol amine is replaced by an equal quantity of guanidine hydrochloride.
- Example 5 The formula of Example 1 except that the amiuoethyl ethanol amine is replaced by an equal quantity of allylamine.
- Example 6 The formula of Example 1 except that the aminoethyl ethanol amine is replaced by 3.0 cc. of sec. amylamine.
- Example 7 The formula of Example 1 except that the aminoethyl ethanol amine is replaced by 18.0 cc. of piperidine.
- Example 8 The formula of Example 1 except that the aminoethyl ethanol amine is replaced by 18.0 cc. of pyrrolidine.
- Example 9 The formula of Example 1 except that the aminoethyl ethanol amine is replaced by 4.5 cc. of trimethylene diamine.
- Example 10 The formula of Example 1 except that the aminoethyl ethanol amine is replaced by 18.0 cc. of n-hydroxyethyl propylene diamine.
- Example 11 The formula of Example 1 except that the barbituric acid is replaced by an equal quantity of cyanuric acid.
- Example 13 The formula of Example 1 except that the barbituric acid is replaced by an equal quantity of urazole.
- Example 14 The formula of Example 1 except that the barbituric acid is replaced by an equal quantity of uracil.
- Example 15 The formula of Example 1 except that the barbituric acid is replaced by an equal quantity of hydantoin.
- Example 16 The formula of Example 1 except that the barbituric acid is replaced by an equal quantity of carboxymethyl barbituric acid.
- Example 17 The formula of Example 1 except that the barbituric acid is replaced by an equal quantity of 4-carboxy uracil.
- Example 1 The formula of Example 1 except that the hydroquinone is replaced by 1.8 gr. of metol.
- Example 20 Water cc 88.5 Sodium carboxymethyl cellulose (high viscosity) Sodium hydroxide gr 8.0 Sodium sulfite gr 2.5 Glycin gr 4.0 Uracil gr- 10.0 Ethylamine/water80%/20% cc 1.75
- Example'21 v 10 Example 22 The formula of Example 20 except that the ethylamine/water is replaced by 1.0 gr. of p-aminophenol.
- Example 23 The formula of Example 20 except that the ethylamine/water is replaced by 0.5 gr. of diaminophenol dihydrochloride.
- Example 24 The formula of Example 20 except that the ethylamine/water is replaced by 1.0 gr. of m-amino benzoic acid.
- Example 25 The formula of Example 20 except that the ethylamine/water is replaced by 0.8 gr. of triethanol amine.
- Example 26 The formula of Example 20 except that the ethylamine/water is replaced by 6 cc. of hydrazine hydrate.
- Example 27 The formula of Example 20 except that the ethylamine/water is replaced by 1.5 gr. symmetrical dimethyl hydrazine dihydrochloride.
- Example 29 The formula of Example 20 except that the ethylamine/water is replaced by 1.5 gr. unsymmetrical dimethyl hydrazine dihydrochloride.
- Example 30 The formula of Example 20 except that the ethylamine/water is replaced by 4.0 gr. of hydroxylamine hydrochloride.
- Example 31 a The formula of Example 20 except that the ethylamine/water is replaced by 2.0 gr. of methyl benzyl hydroxylamine.
- the carboxymethyl cellulose and the sodium hydroxide first were dissolved in the water at room temperature. Next, the sodium sulfite was dissolved in the solution. Thereafter, the cyclic imide was added to the solution and the two phases were mixed until the cyclic imide completely dissolved. Finally the developer and the nitrogenous base were added to the solution With sufficient mixing only to ensure their dissolution, care being taken to prevent oxidation of the developer and volatilization of the nitrogenous base.
- compositions embodying the present invention may be employed in photographic processes other than those involving transfer image formation.
- an alkaline aqueous solution of a cyclic imide and a nitrogenous base is capable of being used as a fixer to dissolve the unreduced silver halide of a gelatino silver halide, preferably hardened, emulsion which has been photoexposed and developed.
- a photographic processing composition comprising, in alkaline aqueous solution, a plurality of agents includ- 5. 1 ing a first complexing agent composed of a cyclic imide characterized by the following general formula:
- Z represents (1) atoms of a series completing a cyclic imide nucleus, said nucleus consisting of from to 6 atoms of which from 1 to 3 are nitrogen and the remainder are carbon and (2) members branching from said atoms of said series, said members being selected from the class consisting of hydrogen atoms, amino radicals, aliphatic radicals containing from 1 to 4 carbon atoms, halogen atoms, keto oxygen atoms and aromatic radicals, at most one of said members being one of said halogen atoms, keto oxygen atoms and aromatic radicals, and a second complexing agent composed of a nitrogenous base selected from the class consisting of ammonia, amines, hydroxylamine, aliphatic hydroxylamines, hydrazine and aliphatic hydrazines, said first complexing agent and said second complexing agent, together, being capable of reacting with silver halide to form water-soluble, complex silver salts, at least one agent of said plurality being a silver halide
- a photographic processing composition comprising, in alkaline aqueous solution, a plurality of agents including a first complexing agent composed of a cyclic imide characterized by the following general formula:
- Z represents (1) atoms of a series completing a from the class consisting of hydrogen atoms, amino radicals, aliphatic radicals containing from 1 to 4 carbon atoms, halogen atoms, keto oxygen atoms and aromatic radicals, at most one of said members being one of said halogen atoms, keto oxygen atoms and aromatic radicals, a second complexing agent composed of a nitrogenous base selected from the class consisting of ammonia, amines, hydroxylamine, aliphatic hydroxylamines, hydrazine and aliphatic hydrazines, said first complexing agent and said second complexing agent, together, being capable of reacting with silver halide to form water-soluble, complex silver salts, and a thickening agent so constituted as to impart to the solution a viscosity of 100 to 200,000 centipoises at C., at least one agent of said plurality being a silver halide developer.
- The'photographic processing composition of claim 4 wherein the alkalinity of said solution ranges from a pH of 11 to a hydroxyl ion concentration of 5 N.
- the photographic process comprising the steps of applying, in a thin layer to a photoexposed gelatino silver halide element, an alkaline aqueous solution of a plurality of agents including a first complexing agent composed of a cyclic imide characterized by the following general formula:
- Z represents (1) atoms of a series completing a cyclic imide nucleus, said nucleus consisting of from 5 to 6 atoms of which from 1 to 3 are nitrogen and the remainder are carbon and (2) members branching from said atoms of said series, said members being selected from the class consisting of hydrogen atoms, amino radicals, aliphatic radicals containing from 1 to 4 carbon atoms, halogen atoms, keto oxygen atoms and aromatic radicals, at most one of said members being one of said halogen atoms, keto oxygen atoms and aromatic radicals, a second complexing agent composed of a nitrogenous base selected from the class consisting of ammonia, amines, hydroxylamine, aliphatic hydroxylamines, hydrazine and aliphatic hydrazines, and a thickening agent so constituted as to impart to the solution a viscosity ranging from to 200,000 centipoises at 20 C., one agent of said plurality being a silver atom
- Z represents (1) atoms of a series completing a cyclic imide nucleus, said nucleus consisting of from 5 to 6 atoms of which from 1 to 3 are nitrogen and the remainder are carbon and (2) members branching from said atoms of said series, said members being selected from the class consisting of hydrogen atoms, amino radicals, aliphatic radicals containing from 1 to 4 carbon atoms, halogen atoms, keto oxygen atoms and aromatic radicals, at most one of said members being one of said halogen atoms, keto oxygen atoms and aromatic radicals, a second complexing agent composed of a nitrogenous base selected from the class consisting of ammonia, amines, hydroxylamine, aliphatic hyd'roxylamines, hydrazine and aliphatic hydrazines, and a thickening agent so constituted as to impart to said solution a viscosity ranging from 100 to 200,000 centipoises at 20 C., one agent of said plurality
- the photographic method of processing a photoexposed silver halide element and an image-receptive element which are in superposed relation comprising the steps of spreading, in a thin layer between said elements, an alkaline aqueous solution of a plurality of agents including a first complexing agent composed of a ⁇ C II 0 wherein Z represent (1) atoms of a series completing a cyclic imide nucleus, said nucleus consisting of from to 6 atoms of which from 1 to 3 are nitrogen and the remainder are carbon and (2) members branching from said atoms of said series, said members being selected from the class consisting of hydrogen atoms, amino radicals, aliphatic radicals containing from 1 to 4 carbon atoms, halogen atoms, keto oxygen atoms and aromatic radicals, at most one of said members being one of said halogen atoms, keto oxygen atoms and aromatic radicals, a second complexing agent composed of a nitrogenous base selected from the class consisting of ammonia, amines,
- a photographic processing composition comprising, in alkaline aqueous solution, a plurality of agents including a first complexing agent composed of a cyclic imide characterized by the following general formula:
- Z represents (1) atoms of a series completing a cyclic imide nucleus, said nucleus consisting of from 5 to 6 atoms of which from 1 to 3 are nitrogen and the remainder are carbon and (2) members branching from said atoms of said series, said members being selected from the class consisting of hydrogen atoms, amino radicals, aliphatic radicals containing from 1 to 4 carbon atoms, halogen atoms, keto oxygen atoms and aromatic radicals, at most one of said members being one of said halogen atoms, keto oxygen atoms and aromatic radicals, a second complexing agent composed of a nitrogenous base selected from the class consisting of ammonia, amines, hydroxylamine, aliphatic hydroxylamines, hydrazine and aliphatic hydrazines, said first complexing agent and said second complexing agent, together, being capable of reacting with silver halide to form watersoluble, complex silver salts, and at least one agent of said plurality being a silver halide
- a photographic process for dissolving silver halide from an exposed, partially developed photosensitive silver halide element including reacting said silver halide, in alkaline aqueous solution, simultaneously with a cyclic imide characterized by the following general formula:
- Z represents (1) atoms of a series completing a cyclic imide nucleus, said nucleus consisting of from 5 to 6 atoms of which from 1 to 3 are nitrogen and the remainder are carbon and (2) members branching from said atoms of said series, said members being selected from the class consisting of hydrogen atoms, amino radicals, aliphatic radicals containing from 1 to 4 carbon atoms, halogen atoms, keto oxygen atoms and aromatic radicals, at most one of said members being one of said halogen atoms, keto oxygen atoms and aromatic radicals, and a nitrogenous base selected from the class consisting of ammonia, amines, hydroxylamine, aliphatic hydroxylamines, hydrazine and aliphatic hydrazines, in order to form a water-soluble complex silver salt.
- concentration of said first complexing agent, by total weight of said solution ranges from 1 to 25% and the concentration of said second complexing agent, by total weight of said solution, ranges from .15 to 15%.
- a process of forming a photographic print comprising the steps of reacting substantially exposed silver halide of a photosensitive silver halide element with a silver halide developer, reacting substantially unreduced silver halide of said photosensitive silver halide element, in alkaline aqueous solution, with a first and a second complexing agent to form a water-soluble silver complex, said first complexing agent being a cyclic imide characterized by the following general formula:
- Z represents (1) atoms of a series completing a cyclic imide nucleus, said nucleus consisting of from 5 to 6 atoms of which from I to 3 are nitrogen and the remainder are carbon and (2) members branching from said atoms of said series, said members being selected from the class consisting of hydrogen atoms, amino radicals, aliphatic radicals containing from 1 to 4 carbon atoms, halogen atoms, keto oxygen atoms and aromatic radicals, at most one of said members being one of said halogen atoms, keto oxygen atoms and aromatic radicals, said second complexing agent being a nitrogenous base, transferring said complex by dilfusion to an image-receptive material, and forming, at said receptive material, an image incorporating silver from said silver complex.
- the photographic process of claim 15 including a thickening agent so constituted as to impart to the solution a viscosity ranging from to 200,000 centipoises at 20 C.
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- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NLAANVRAGE8000537,A NL189766B (nl) | 1953-09-04 | Waterige metaalbewerkingsvloeistof. | |
NL95865D NL95865C (es) | 1953-09-04 | ||
US378684A US2857274A (en) | 1953-09-04 | 1953-09-04 | Photographic compositions and processes |
GB19882/54A GB751304A (en) | 1953-09-04 | 1954-07-07 | Improvements in photographic processing compositions and in photographic silver image transfer processes |
DEI9091A DE1012176B (de) | 1953-09-04 | 1954-09-01 | Verfahren zur Herstellung von Bildern nach dem Silbersalzdiffusionsverfahren und Mittel zur Durchfuehrung des Verfahrens |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US378684A US2857274A (en) | 1953-09-04 | 1953-09-04 | Photographic compositions and processes |
Publications (1)
Publication Number | Publication Date |
---|---|
US2857274A true US2857274A (en) | 1958-10-21 |
Family
ID=23494118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US378684A Expired - Lifetime US2857274A (en) | 1953-09-04 | 1953-09-04 | Photographic compositions and processes |
Country Status (4)
Country | Link |
---|---|
US (1) | US2857274A (es) |
DE (1) | DE1012176B (es) |
GB (1) | GB751304A (es) |
NL (2) | NL189766B (es) |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3061453A (en) * | 1959-08-03 | 1962-10-30 | Polaroid Corp | Process for incorporating photographic reagents in a photographic element using a common solvent and a preferential solvent |
US3174859A (en) * | 1959-09-24 | 1965-03-23 | Gevaert Photo Prod Nv | Process for obtaining multiple photographic positive images by diffusiontransfer |
US3343958A (en) * | 1965-04-09 | 1967-09-26 | Polaroid Corp | Monobath containing cysteine-nitrogenous base combination |
US3362961A (en) * | 1963-06-26 | 1968-01-09 | Polaroid Corp | N-substituted hydroxylamines |
US3406064A (en) * | 1965-02-02 | 1968-10-15 | Polaroid Corp | Diffusion transfer with 4-methylphenylhydroquinone in the emulsion and n,n-diethylhydroxylamine in the processing fluid |
US3619185A (en) * | 1968-04-29 | 1971-11-09 | Polaroid Corp | Photographic processing compositions and processes using same |
US3723117A (en) * | 1969-10-27 | 1973-03-27 | Agfa Gevaert | Method for developing silver halide emulsions |
DE2263015A1 (de) * | 1971-12-23 | 1973-07-05 | Polaroid Corp | Photographisches material |
US4021249A (en) * | 1974-09-12 | 1977-05-03 | Fuji Photo Film Co., Ltd. | Heat developable light-sensitive material incorporating a substituted s-triazine-2,4,6-(1H, 3H, 5H)-trione reducing agent |
FR2408855A1 (fr) * | 1977-11-09 | 1979-06-08 | Polaroid Corp | Nouvelle composition de traitement photographique |
US4259114A (en) * | 1979-12-31 | 1981-03-31 | Polaroid Corporation | Method for forming silver precipitating nuclei |
US4259116A (en) * | 1979-12-31 | 1981-03-31 | Polaroid Corporation | Method for forming silver precipitating nuclei |
US4259115A (en) * | 1979-12-31 | 1981-03-31 | Polaroid Corporation | Method for forming silver precipitating nuclei |
US4267255A (en) * | 1979-04-24 | 1981-05-12 | Polaroid Corporation | Novel photographic processing composition |
US4297430A (en) * | 1979-05-02 | 1981-10-27 | Mitsubishi Paper Mills, Ltd. | Photographic material for production of printing plates and method for production of printing plates |
US4396699A (en) * | 1980-09-30 | 1983-08-02 | Agfa-Gevaert, N.V. | Process for the production of a multicolor image by image-wise dye diffusion transfer |
US4526857A (en) * | 1983-04-20 | 1985-07-02 | Fuji Photo Film Co., Ltd. | Image formation by silver salt diffusion transfer process comprising mercaptotriazole and thiouracil |
DE3506712A1 (de) * | 1984-02-27 | 1985-08-29 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | Verfahren zur herstellung eines abbildes durch silberhalogenid-diffusionsuebertragung |
JPS60194448A (ja) * | 1984-03-16 | 1985-10-02 | Fuji Photo Film Co Ltd | 銀画像の形成方法 |
US4713313A (en) * | 1984-05-02 | 1987-12-15 | Polaroid Corporation | Photographic system and novel compounds |
US4892811A (en) * | 1984-10-16 | 1990-01-09 | Fuji Photo Film Co., Ltd. | Silver halide photographic material |
US5132201A (en) * | 1988-04-21 | 1992-07-21 | Fuji Photo Film Co., Ltd. | Silver halide photographic material with redox releaser |
EP0786690A2 (en) | 1996-01-26 | 1997-07-30 | Eastman Kodak Company | Silver halide light sensitive emulsion layer having enhanced photographic sensitivity |
EP0796881A1 (en) * | 1996-03-22 | 1997-09-24 | Shimadzu Corporation | Process for preparing polylactic acid |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL226676A (es) * | 1957-04-17 | |||
GB912754A (en) * | 1959-08-19 | 1962-12-12 | Polaroid Corp | Photographic colour transfer process and product |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1958609A (en) * | 1932-01-15 | 1934-05-15 | Squibb & Sons Inc | Hypnotic preparation |
US2017279A (en) * | 1935-10-15 | Process for making readily soluble | ||
US2225384A (en) * | 1940-12-17 | Printing colors and process of | ||
US2354232A (en) * | 1944-07-25 | Cox n nh | ||
US2543181A (en) * | 1947-01-15 | 1951-02-27 | Polaroid Corp | Photographic product comprising a rupturable container carrying a photographic processing liquid |
US2590775A (en) * | 1949-04-11 | 1952-03-25 | Ilford Ltd | Silver halide emulsion containing a thio-imino-urazole as a stabilizer |
US2599518A (en) * | 1951-04-25 | 1952-06-03 | Edwal Lab Inc | High contrast photographic developers |
US2635048A (en) * | 1948-07-06 | 1953-04-14 | Polaroid Corp | Photographic transfer product and process |
US2697100A (en) * | 1952-05-31 | 1954-12-14 | Eastman Kodak Co | Alpha-acylthio-n(2-benzothiazolyl) succinimides |
-
0
- NL NL95865D patent/NL95865C/xx active
- NL NLAANVRAGE8000537,A patent/NL189766B/xx unknown
-
1953
- 1953-09-04 US US378684A patent/US2857274A/en not_active Expired - Lifetime
-
1954
- 1954-07-07 GB GB19882/54A patent/GB751304A/en not_active Expired
- 1954-09-01 DE DEI9091A patent/DE1012176B/de active Pending
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2017279A (en) * | 1935-10-15 | Process for making readily soluble | ||
US2225384A (en) * | 1940-12-17 | Printing colors and process of | ||
US2354232A (en) * | 1944-07-25 | Cox n nh | ||
US1958609A (en) * | 1932-01-15 | 1934-05-15 | Squibb & Sons Inc | Hypnotic preparation |
US2543181A (en) * | 1947-01-15 | 1951-02-27 | Polaroid Corp | Photographic product comprising a rupturable container carrying a photographic processing liquid |
US2635048A (en) * | 1948-07-06 | 1953-04-14 | Polaroid Corp | Photographic transfer product and process |
US2590775A (en) * | 1949-04-11 | 1952-03-25 | Ilford Ltd | Silver halide emulsion containing a thio-imino-urazole as a stabilizer |
US2599518A (en) * | 1951-04-25 | 1952-06-03 | Edwal Lab Inc | High contrast photographic developers |
US2697100A (en) * | 1952-05-31 | 1954-12-14 | Eastman Kodak Co | Alpha-acylthio-n(2-benzothiazolyl) succinimides |
Cited By (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3061453A (en) * | 1959-08-03 | 1962-10-30 | Polaroid Corp | Process for incorporating photographic reagents in a photographic element using a common solvent and a preferential solvent |
US3174859A (en) * | 1959-09-24 | 1965-03-23 | Gevaert Photo Prod Nv | Process for obtaining multiple photographic positive images by diffusiontransfer |
US3362961A (en) * | 1963-06-26 | 1968-01-09 | Polaroid Corp | N-substituted hydroxylamines |
US3406064A (en) * | 1965-02-02 | 1968-10-15 | Polaroid Corp | Diffusion transfer with 4-methylphenylhydroquinone in the emulsion and n,n-diethylhydroxylamine in the processing fluid |
US3343958A (en) * | 1965-04-09 | 1967-09-26 | Polaroid Corp | Monobath containing cysteine-nitrogenous base combination |
US3619185A (en) * | 1968-04-29 | 1971-11-09 | Polaroid Corp | Photographic processing compositions and processes using same |
US3723117A (en) * | 1969-10-27 | 1973-03-27 | Agfa Gevaert | Method for developing silver halide emulsions |
DE2263015A1 (de) * | 1971-12-23 | 1973-07-05 | Polaroid Corp | Photographisches material |
JPS4874223A (es) * | 1971-12-23 | 1973-10-06 | ||
JPS5748777B2 (es) * | 1971-12-23 | 1982-10-18 | ||
US4021249A (en) * | 1974-09-12 | 1977-05-03 | Fuji Photo Film Co., Ltd. | Heat developable light-sensitive material incorporating a substituted s-triazine-2,4,6-(1H, 3H, 5H)-trione reducing agent |
FR2408855A1 (fr) * | 1977-11-09 | 1979-06-08 | Polaroid Corp | Nouvelle composition de traitement photographique |
US4168166A (en) * | 1977-11-09 | 1979-09-18 | Polaroid Corporation | Photographic processing composition comprising borate |
US4267255A (en) * | 1979-04-24 | 1981-05-12 | Polaroid Corporation | Novel photographic processing composition |
US4297430A (en) * | 1979-05-02 | 1981-10-27 | Mitsubishi Paper Mills, Ltd. | Photographic material for production of printing plates and method for production of printing plates |
US4259115A (en) * | 1979-12-31 | 1981-03-31 | Polaroid Corporation | Method for forming silver precipitating nuclei |
US4259116A (en) * | 1979-12-31 | 1981-03-31 | Polaroid Corporation | Method for forming silver precipitating nuclei |
US4259114A (en) * | 1979-12-31 | 1981-03-31 | Polaroid Corporation | Method for forming silver precipitating nuclei |
US4396699A (en) * | 1980-09-30 | 1983-08-02 | Agfa-Gevaert, N.V. | Process for the production of a multicolor image by image-wise dye diffusion transfer |
US4526857A (en) * | 1983-04-20 | 1985-07-02 | Fuji Photo Film Co., Ltd. | Image formation by silver salt diffusion transfer process comprising mercaptotriazole and thiouracil |
US4624911A (en) * | 1984-02-27 | 1986-11-25 | Fuji Photo Film Co., Ltd. | Silver halide diffusion transfer using plural cyclic imide silver halide solvents |
DE3506712A1 (de) * | 1984-02-27 | 1985-08-29 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | Verfahren zur herstellung eines abbildes durch silberhalogenid-diffusionsuebertragung |
JPS60194448A (ja) * | 1984-03-16 | 1985-10-02 | Fuji Photo Film Co Ltd | 銀画像の形成方法 |
JPH0554663B2 (es) * | 1984-03-16 | 1993-08-13 | Fuji Photo Film Co Ltd | |
US4713313A (en) * | 1984-05-02 | 1987-12-15 | Polaroid Corporation | Photographic system and novel compounds |
US4892811A (en) * | 1984-10-16 | 1990-01-09 | Fuji Photo Film Co., Ltd. | Silver halide photographic material |
US5132201A (en) * | 1988-04-21 | 1992-07-21 | Fuji Photo Film Co., Ltd. | Silver halide photographic material with redox releaser |
EP0786690A2 (en) | 1996-01-26 | 1997-07-30 | Eastman Kodak Company | Silver halide light sensitive emulsion layer having enhanced photographic sensitivity |
EP0796881A1 (en) * | 1996-03-22 | 1997-09-24 | Shimadzu Corporation | Process for preparing polylactic acid |
US5821327A (en) * | 1996-03-22 | 1998-10-13 | Shimadzu Corporation | Process for preparing polylactic acid |
Also Published As
Publication number | Publication date |
---|---|
DE1012176B (de) | 1957-07-11 |
NL189766B (nl) | |
NL95865C (es) | |
GB751304A (en) | 1956-06-27 |
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