US3026201A - Antifoggants and stabilizers for photographic silver halide emulsions - Google Patents
Antifoggants and stabilizers for photographic silver halide emulsions Download PDFInfo
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- US3026201A US3026201A US790325A US79032559A US3026201A US 3026201 A US3026201 A US 3026201A US 790325 A US790325 A US 790325A US 79032559 A US79032559 A US 79032559A US 3026201 A US3026201 A US 3026201A
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- 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
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/34—Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
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- 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
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/34—Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
- G03C1/346—Organic derivatives of bivalent sulfur, selenium or tellurium
Definitions
- This invention relates to the stabilization of photographic materials. More particularly, this invention relates to light-sensitive photographic silver halide emulsions containing 1,3-disubstituted 2 benzimidazolinethiones as stabilizing and antifogging agents, and to methods of producing photographic emulsions containing them.
- stabilizing and/or antifogging agents often are characterized by deleterious side reactions which adversely affect the light-sensitive emulsion.
- the incorporation of stabilizing and/or antifogging agents of the prior art cause an excessive loss of speed and/or contrast of the emulsion.
- optical sensitization or dye sensitizing may be adversely affected, a condition which is probably attributed to displacement of the sensitizing dye from the silver halide grain surface by the stabilizing agent.
- 1,3-disubstituted-2- benzimidazolinethiones are eminently suitable as antifoggants and/ or stabilizers for light-sensitive silver halide emulsions and, furthermore, are capable of performing their function Without interfering or deleteriously affecting the speed aud/ or contrast, optical sensitization or dye sensitization of the emulsion in which they are incorpo rated.
- l,3-disubstituted-2-benzimidazolinethiones may be represented by the following general formula:
- R represents a hydroxyl group or an amino group of the formula NR R wherein R and R represent hydrogen, an alkyl group, i.e., methyl, ethyl, propyl, butyl, isobutyl, amyl, isoamyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl,- pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, etc., a lower aralkyl group, wherein the aryl rings can be a monocyclic 3,025,201 Patented Mar.
- R and R can complete a heterocyclic ring structure of the pyrrolidine, piperidine, morpholine and thiazine series.
- sired product this can be obtained by the reaction of the corresponding Z-benzimidazolinethione and formaldehyde in aqueous solution under refiux.
- Secondary amines which can be used to form the 1,3- disubstituted-2-benzimidazolinethiones include secondary alkylamines, i.e., dimethylamine, methylethylamine, diethylamine, dipropylamine, methylbutylamine, dibutylamine, propylbutylamine, amylpropylamine, methylhexylamine, methylheptylamine, methyloctylamine, ethylnonylamine, methyldecylamine, propylundecylamine, etc. and heterocyclic amines of the pyrrolidine series, piperidine series, morpholine series, thiazine series and diazine series.
- secondary alkylamines i.e., dimethylamine, methylethylamine, diethylamine, dipropylamine, methylbutylamine, dibutylamine, propylbutylamine, amyl
- the antifogging and/or stabilizing agents of our invention can be incorporated or contacted with a silver halide photographic emulsion at any of the various stages during its processing. Thus, they may be added as ripening finals or as coating finals. Ripening finals are added during the ripening or sensitivity increasing stage of the emulsion-making process and such addition may be made before, during or after the addition of the soluble silver salt to the soluble halide in the presence of a suitable colloid such as gelatin, polyvinyl alcohol, solubilized casein, albumin, carboxymethyl cellulose, zein or the like.
- a suitable colloid such as gelatin, polyvinyl alcohol, solubilized casein, albumin, carboxymethyl cellulose, zein or the like.
- the compounds of the present invention are combined with the emulsion just prior to coating and when maximum sensitivity has almost been achieved.
- Such emulsions can then becoated on the usual supports familiar to the art as exemplified by glass, paper, metal, or film base such as cellulose triacetate, polyterephthalate esters, etc.
- the antifogging and stabilizing compounds may be desirable to apply in separate layers adjacent to the emulsion as, for instance, in a separate undercoating layer or in the antiabrasiongelatin surface. Under different circumstances, the desired result may best be attained by adding the antifoggant and/or stabilizer to one or perhaps all of the processingbaths for the involved emulsion.
- the aforesaid 1,3-disubstituted-Z-benzimidazolinethiones of our invention are advantageously used in concentrations of 0.1 to mg.
- the concentration can be varied from 1 to mg. per 0.6 mole of silver halide. As the concentration de pends primarily. on the type of emulsion employed, it is advisable to determine the optimum quantities of antifoggant and/ or stabilizer in each instance.
- the nonsensitized orthochrornatic, panchromatic, X-ray, paper and color emulsions are typical.
- 1,3-disubstituted-2-benzimidazolinethiones are effective by themselves, they may be used in combination with the various other adjuncts that are commonly added to photographic emulsions such as sulfur sensitizers, reduction and metal sensitizers, noble metal sensitizers or accelerators such as polyoxyethylenes and their derivatives or polyvinylpyrrolidone.
- our stabilizers and/or antifoggants'do not interfere with the optical sensitization of the silver halide emulsions by displacing the sensitizing dye from the silver halide grain surface.
- Example I A gelatin-silver halide emulsion containing 2% silver iodide and 98% silver bromide was prepared in a conventional manner and brought up to its maximum lightsensitivity. It was then readied for coating. Finals were added such as sensitizing dyes, stabilizers and hardening agents. A 0.1% solution of 1,3 -bis[(1-piperidyl) methyl]- 2-benzimidazolinethione in methanol was prepared and added to the emulsion as an antifoggant and stabilizer. The emulsion samples contained about 0.6 mole of silver halide. The so prepared emulsion samples were coated on a suitable cellulose ester base and dried. Samples of these film coatings were then exposed in a Type IIB Sensitometer and developed in a developer of the following composition:
- Example II Example III The same procedure was followed as given in Example I except that the stabilizer was 1,3-bis (hydroxymethyD-Z- benzimidazolinethione. The results are summarized in the following table:
- Example 1V The same procedure was followed as given in Example Iexcept that the stabilizer was l,3-bis(N,N-diethylaminomethyl)-2-benzimidazolinethione. The results are summarized in the following table:
- Example V The same procedure was carried out as given in Example I except that a conventional stabilizer was also present in the photographic emulsion.
- the results are summar- 1.
- R is selected from the group consisting of an OH group, a NR R group, wherein R and R are selected from the class consisting of hydrogen, an alkyl group, an aromatic group selected from the class consisting of benzene and naphthalene, an aralkyl group selected from the class consisting of phenethyl and naphthyl, a heterccyclic radical selected from the class consisting of pyrrolidino, piperidino, thiazino, diazino and morpholino.
- a light-sensitive photographic element comprising a base and a coating of gelatino-silver halide emulsion thereon, said emulsion containing an antifogging and stabilizing compound having the following chemical structure:
- R is selected from the group consisting of an OH group, a NR R group, wherein'R and R are each selected from the class consisting of hydrogen, an alkyl group, an aromatic group selected from the class consisting of benzene and naphthalene, an aralkyl group selected from the class consisting of phenethyl and naphthylethyl and heterocyclic radicals selected from the class consisting of pyrrolidino, piperidino, thiazino, diazino and morpholino.
- a light-sensitive structure comprising a base, a layer of light-sensitive silver halide emulsion thereon, and a separate layer adjacent said first mentioned layer containing an antifogging and stabilizing compound having the following chemical structure:
- R is selected from the group consisting of an OH group and an amino group NR R wherein R and R are each selected from the group consisting of hydrogen, an alkyl group, an aromatic group selected from the class consisting of benzene and naphthalene, an aralkyl group selected from the class consisting of phenethyl and naphthylethyl, a heterocyclic radical selected from the class consisting of pyrrolidino, piperidino, thiazino, diazino and morpholino.
- a process of forming a silver halide photographic emulsion having a reduced tendency to fog which comprises forming the emulsions, ripening the emulsion and during said ripening adding thereto a compound having the following chemical structure:
- R is selected from the group consisting of an OH group and an amino group -NR R wherein R and R are each selected from the group consisting of hydrogen, an alkyl group, an aromatic group selected from the class consisting of benzene and naphthalene, an aralkyl group selected from the class consisting of phenethyl and naphthylethyl, a heterocyclic radical selected from the class consisting of pyrrolidino, pipen'dino, thiazino, diazino and morpholino.
- a process of forming a silver halide light-sensitive 7 photographic element having a reduced tendency to fog which comprises forming an emulsion, ripening said emulsion, adding to said emulsion just prior to the coating of same, a compound having the following chemical structure c HER 1T7 CHER wherein R is selected from the group consisting of an OH group and an amino group --NR R wherein R and R are each selected from the group consisting of hydrogen, an alkyl group, an aromatic group selected References Cited in the file of this patent UNITED STATES PATENTS 2,353,754' Peterson July 18, 1944 2,384,593 Bean Sept. 11, 1945 FOREIGN PATENTS 1,001,730 France Oct. 24, 1951
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- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
United States Patent 3,026,201 ANTIFOGGANTS AND STABILIZERS FOR PHOTO- GRAPHIC SILVER HALIDE EMULSIONS Emil B. Ranch and Fritz Dersch, Binghamton, N.Y., as-
signors to General Aniline & Film Corporation, New York, N.Y., a corporation of Delaware No Drawing. Filed Feb. 2, 1959, Ser. No. 790,325 12 Claims. (Cl. 9667) This invention relates to the stabilization of photographic materials. More particularly, this invention relates to light-sensitive photographic silver halide emulsions containing 1,3-disubstituted 2 benzimidazolinethiones as stabilizing and antifogging agents, and to methods of producing photographic emulsions containing them.
It is well known in the photographic art that lightsensitive emulsions such as gelatin-silver halide emulsions have an inherent tendency to fog. Conditions under which fogging occurs are: prolonged ripening of the emulsions, storage over prolonged periods of time especially under conditions of elevated temperature and by prolonged developing. These troublesome properties of photographic emulsions have long harassed the art and numerous remedies have been proposed to overcome them. Thus, it is the practice to add certain chemical compounds such as benzimidazole and its derivatives, particularly Z-mercaptobenzimidazole, to photographic emulsions to increase their stability and reduce their tendency to fog. However, such compounds, referred to in the art as stabilizing and/or antifogging agents, as used heretofore, often are characterized by deleterious side reactions which adversely affect the light-sensitive emulsion. In many instances, the incorporation of stabilizing and/or antifogging agents of the prior art cause an excessive loss of speed and/or contrast of the emulsion. in some cases, optical sensitization or dye sensitizing may be adversely affected, a condition which is probably attributed to displacement of the sensitizing dye from the silver halide grain surface by the stabilizing agent.
It has now been discovered that 1,3-disubstituted-2- benzimidazolinethiones are eminently suitable as antifoggants and/ or stabilizers for light-sensitive silver halide emulsions and, furthermore, are capable of performing their function Without interfering or deleteriously affecting the speed aud/ or contrast, optical sensitization or dye sensitization of the emulsion in which they are incorpo rated.
The use of the aforesaid compounds to inhibit fog and to stabilize silver halide emulsions either by incorporating the same in the emulsion or in layers adjacent thereto, or in processing baths for such emulsions constitutes the purposes and objects of the present invention.
The l,3-disubstituted-2-benzimidazolinethiones, the use of which is contemplated herein as stabilizers or antifoggants, may be represented by the following general formula:
CHnR
wherein R represents a hydroxyl group or an amino group of the formula NR R wherein R and R represent hydrogen, an alkyl group, i.e., methyl, ethyl, propyl, butyl, isobutyl, amyl, isoamyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl,- pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, etc., a lower aralkyl group, wherein the aryl rings can be a monocyclic 3,025,201 Patented Mar. 20, 1962 or bicyclic aromatic nucleus, i.e., benzyl, phenethyl, naphthylmethyl, naphthylethyl, etc., or R and R can complete a heterocyclic ring structure of the pyrrolidine, piperidine, morpholine and thiazine series.
Examples of compounds which fall within the scope of the above formula and which are effective as antifoggants or stabilizers for the purpose of practicing the invention are typified in the following formulate:
C I'Ig The 1,3-disubstituted-2-benzimidazolinethiones of the type employed herein are described in the chemical literature. For instance, representative members of the aforesaid class of compounds can be synthesized according to the method of H. Zinner et al., Berichte 90, page 2852 (1957). The method described therein is an adaptation of the Mannich reaction in which a Z-benzimidazolinethione, formalin and an amine are reacted to give the 1,3-bis-aminomethylbenzimidazolinethione. The reaction is normally carried out in a lower alcoholic solvent at elevated temperatures such as those prevailing at the boiling point of the particular solvent employed. If the 1,3-bis-hydroxymethylbenzirnidazolinethione is the de-.
sired product, this can be obtained by the reaction of the corresponding Z-benzimidazolinethione and formaldehyde in aqueous solution under refiux.
Secondary amines which can be used to form the 1,3- disubstituted-2-benzimidazolinethiones include secondary alkylamines, i.e., dimethylamine, methylethylamine, diethylamine, dipropylamine, methylbutylamine, dibutylamine, propylbutylamine, amylpropylamine, methylhexylamine, methylheptylamine, methyloctylamine, ethylnonylamine, methyldecylamine, propylundecylamine, etc. and heterocyclic amines of the pyrrolidine series, piperidine series, morpholine series, thiazine series and diazine series.
The antifogging and/or stabilizing agents of our invention can be incorporated or contacted with a silver halide photographic emulsion at any of the various stages during its processing. Thus, they may be added as ripening finals or as coating finals. Ripening finals are added during the ripening or sensitivity increasing stage of the emulsion-making process and such addition may be made before, during or after the addition of the soluble silver salt to the soluble halide in the presence of a suitable colloid such as gelatin, polyvinyl alcohol, solubilized casein, albumin, carboxymethyl cellulose, zein or the like. When added as coating finals, the compounds of the present invention are combined with the emulsion just prior to coating and when maximum sensitivity has almost been achieved. Such emulsions can then becoated on the usual supports familiar to the art as exemplified by glass, paper, metal, or film base such as cellulose triacetate, polyterephthalate esters, etc.
In some instances, it may be desirable to apply the antifogging and stabilizing compounds in separate layers adjacent to the emulsion as, for instance, in a separate undercoating layer or in the antiabrasiongelatin surface. Under different circumstances, the desired result may best be attained by adding the antifoggant and/or stabilizer to one or perhaps all of the processingbaths for the involved emulsion.
When used as ripening finals, the aforesaid 1,3-disubstituted-Z-benzimidazolinethiones of our invention are advantageously used in concentrations of 0.1 to mg.
per 0.6 mole of silver halide. In the caseof coating finals, the concentration can be varied from 1 to mg. per 0.6 mole of silver halide. As the concentration de pends primarily. on the type of emulsion employed, it is advisable to determine the optimum quantities of antifoggant and/ or stabilizer in each instance.
Of the various types of emulsions which can be stabilized with our antifoggants and/or stabilizers, the nonsensitized orthochrornatic, panchromatic, X-ray, paper and color emulsions are typical.
Although the aforesaid 1,3-disubstituted-2-benzimidazolinethiones are effective by themselves, they may be used in combination with the various other adjuncts that are commonly added to photographic emulsions such as sulfur sensitizers, reduction and metal sensitizers, noble metal sensitizers or accelerators such as polyoxyethylenes and their derivatives or polyvinylpyrrolidone.
As previously pointed out, our stabilizers and/or antifoggants'do not interfere with the optical sensitization of the silver halide emulsions by displacing the sensitizing dye from the silver halide grain surface.
The following examples are given to illustrate the manner in which the antifoggants and/or stabilizers of our invention can be used. It is to be understood, however, that these examples are illustrative only and in no way are to be construed as limiting the invention.
Example I A gelatin-silver halide emulsion containing 2% silver iodide and 98% silver bromide was prepared in a conventional manner and brought up to its maximum lightsensitivity. It was then readied for coating. Finals were added such as sensitizing dyes, stabilizers and hardening agents. A 0.1% solution of 1,3 -bis[(1-piperidyl) methyl]- 2-benzimidazolinethione in methanol was prepared and added to the emulsion as an antifoggant and stabilizer. The emulsion samples contained about 0.6 mole of silver halide. The so prepared emulsion samples were coated on a suitable cellulose ester base and dried. Samples of these film coatings were then exposed in a Type IIB Sensitometer and developed in a developer of the following composition:
Metol a 1.5 Sodium sulfite, anhydrous 45 Sodium bisulfite 1 Hydroquinone 3 Sodium carbonate, monohydrated 6 Potassium bromide 0.8 Water to make 1 liter.
The results obtained are summarized in the following table:
Oven Fog at 4 Minute Development Fog at 12 Minute Development Relative Speed Oven Quantity of Compound Added Speed The 1,3 bis [(l-piperidyDmethyl]-2-benzimidazolinethione, used as described'above, was prepared according to the method of H. Zinner et al. given in the aforementioned Ber. 90, p. 2852 (1957) and was carried out as follows: a i
15 grams of 2-benzimidazolinethione was suspended in 100 ml. of methanol to which was then added 22 ml. of piperidine and 23 ml. of a 35% aqueous formaldehyde solution. The resulting mixture evolved heat and a clear solution was formed. On cooling, a crystalline product came down which was crystallized from petroleum ether. The melting point of the pure compound was 124-125 C.
Example II Example III The same procedure was followed as given in Example I except that the stabilizer was 1,3-bis (hydroxymethyD-Z- benzimidazolinethione. The results are summarized in the following table:
Fog at 12 Minute Devel-.
opment Oven Fog at 4 Minute Development Relative Speed Oven Quantity of Compound Added Speed The preparation of the 1,3-bis(hydroxymethyl)-2 benzimidazolinethione was carried out according to the Zinner method as disclosed above.
Example 1V The same procedure was followed as given in Example Iexcept that the stabilizer was l,3-bis(N,N-diethylaminomethyl)-2-benzimidazolinethione. The results are summarized in the following table:
Fog at 12 Oven Quantity of Compound Relative Minute Oven Fog at 4 Added Speed Devel- Speed Minute opmcnt Development The 1,3 bis(N,N-diethylaminomethyl)-2-bcnzimidazolinethione was obtained using the Zinner method given above.
Example V The same procedure was carried out as given in Example I except that a conventional stabilizer was also present in the photographic emulsion. The results are summar- 1. A light-sensitive silver halide emulsion containing an antifogging and stabilizing compound having the following chemical structure:
CHgR
HRR
wherein R is selected from the group consisting of an OH group, a NR R group, wherein R and R are selected from the class consisting of hydrogen, an alkyl group, an aromatic group selected from the class consisting of benzene and naphthalene, an aralkyl group selected from the class consisting of phenethyl and naphthyl, a heterccyclic radical selected from the class consisting of pyrrolidino, piperidino, thiazino, diazino and morpholino.
2. A light-sensitive silver halide emulsion as recited in claim 1 wherein the antifogging and stabilizing compound is 1,3-bis[(4-rnorpholinyl)methyl]-2-benzimidazolinethione.
3. A light-sensitive silver halide emulsion as recited in claim 1 wherein the antifogging and stabilizing compound is l,3-bis[( l-piperidyl)methyl]-2-benzimida2olinethione.
4. A light-sensitive silver halide emulsion as recited in claim 1 wherein the antifogging and stabilizing compound is l,3-bis(hydroxymethyl)-2-benzimidazolinethione.
5. A light-sensitive silver halide emulsion as recited in claim 1 wherein the antifogging and stabilizing compound is l,3-bis(diethylaminomethyl)-2benzimidazolinethione.
6. A light-sensitive silver halide emulsion as recited in claim 1 wherein the antifogging and stabilizing compound is present in the emulsion in the ratio of 0.1 to 30 mg. per 0.6 mole of silver halide.
7. A light-sensitive silver halide emulsion as recited in claim 1 wherein the antifogging and stabilizing compound is present in the emulsion in the ratio of 0.1 to 25 mg. per 0.6 mole of silver halide.
8. A light-sensitive silver halide emulsion as recited in claim 1 wherein the antifogging and stabilizing compound is present in the emulsion in the ratio of 0.1 to 30 mg. per 0.6' mole of silver halide.
9. A light-sensitive photographic element comprising a base and a coating of gelatino-silver halide emulsion thereon, said emulsion containing an antifogging and stabilizing compound having the following chemical structure:
wherein R is selected from the group consisting of an OH group, a NR R group, wherein'R and R are each selected from the class consisting of hydrogen, an alkyl group, an aromatic group selected from the class consisting of benzene and naphthalene, an aralkyl group selected from the class consisting of phenethyl and naphthylethyl and heterocyclic radicals selected from the class consisting of pyrrolidino, piperidino, thiazino, diazino and morpholino.
10. A light-sensitive structure comprising a base, a layer of light-sensitive silver halide emulsion thereon, and a separate layer adjacent said first mentioned layer containing an antifogging and stabilizing compound having the following chemical structure:
wherein R is selected from the group consisting of an OH group and an amino group NR R wherein R and R are each selected from the group consisting of hydrogen, an alkyl group, an aromatic group selected from the class consisting of benzene and naphthalene, an aralkyl group selected from the class consisting of phenethyl and naphthylethyl, a heterocyclic radical selected from the class consisting of pyrrolidino, piperidino, thiazino, diazino and morpholino.
11. A process of forming a silver halide photographic emulsion having a reduced tendency to fog which comprises forming the emulsions, ripening the emulsion and during said ripening adding thereto a compound having the following chemical structure:
CHgR
wherein R is selected from the group consisting of an OH group and an amino group -NR R wherein R and R are each selected from the group consisting of hydrogen, an alkyl group, an aromatic group selected from the class consisting of benzene and naphthalene, an aralkyl group selected from the class consisting of phenethyl and naphthylethyl, a heterocyclic radical selected from the class consisting of pyrrolidino, pipen'dino, thiazino, diazino and morpholino.
12. A process of forming a silver halide light-sensitive 7 photographic element having a reduced tendency to fog which comprises forming an emulsion, ripening said emulsion, adding to said emulsion just prior to the coating of same, a compound having the following chemical structure c HER 1T7 CHER wherein R is selected from the group consisting of an OH group and an amino group --NR R wherein R and R are each selected from the group consisting of hydrogen, an alkyl group, an aromatic group selected References Cited in the file of this patent UNITED STATES PATENTS 2,353,754' Peterson July 18, 1944 2,384,593 Bean Sept. 11, 1945 FOREIGN PATENTS 1,001,730 France Oct. 24, 1951
Claims (1)
1. A LIGHT-SENSITIVE SILVER HALIDE EMULSION CONTAINING AN ANTIFOGGING AND STABILIZING COMPOUND HAVING THE FOLLOWING CHEMICAL STRUCTURE:
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| Application Number | Priority Date | Filing Date | Title |
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| US790325A US3026201A (en) | 1959-02-02 | 1959-02-02 | Antifoggants and stabilizers for photographic silver halide emulsions |
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| US790325A US3026201A (en) | 1959-02-02 | 1959-02-02 | Antifoggants and stabilizers for photographic silver halide emulsions |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3161520A (en) * | 1962-12-11 | 1964-12-15 | Gen Aniline & Film Corp | Fog reduction in photographic silver halide emulsions |
| US3252799A (en) * | 1962-06-09 | 1966-05-24 | Agfa Ag | Stabilized silver halide emulsions |
| US3617289A (en) * | 1966-12-10 | 1971-11-02 | Fuji Photo Film Co Ltd | Stabilization process for thermally developable light-sensitive elements |
| DE2210369A1 (en) * | 1971-03-04 | 1972-09-28 | Fuji Photo Film Co. Ltd., Ashigara-Kamigun, Kanagawa (Japan) | Process for the production of photographic images |
| DE2263808A1 (en) * | 1971-12-28 | 1973-07-05 | Fuji Photo Film Co Ltd | LIGHT SENSITIVE SILVER HALOGENIDE MATERIAL |
| US4892812A (en) * | 1983-02-04 | 1990-01-09 | Mitsubishi Paper Mills, Ltd. | Silver halide photosensitive materials |
| US5108884A (en) * | 1990-03-30 | 1992-04-28 | Mitsubishi Paper Mills Limited | Antistatically finished silver halide photographic photosensitive material |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2353754A (en) * | 1942-11-07 | 1944-07-18 | Eastman Kodak Co | Color photography using metallic salt coupler compounds |
| US2384593A (en) * | 1943-08-06 | 1945-09-11 | Eastman Kodak Co | Antifoggant |
| FR1001730A (en) * | 1948-01-13 | 1952-02-27 | Kodak Pathe | advanced photographic emulsions |
-
1959
- 1959-02-02 US US790325A patent/US3026201A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2353754A (en) * | 1942-11-07 | 1944-07-18 | Eastman Kodak Co | Color photography using metallic salt coupler compounds |
| US2384593A (en) * | 1943-08-06 | 1945-09-11 | Eastman Kodak Co | Antifoggant |
| FR1001730A (en) * | 1948-01-13 | 1952-02-27 | Kodak Pathe | advanced photographic emulsions |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3252799A (en) * | 1962-06-09 | 1966-05-24 | Agfa Ag | Stabilized silver halide emulsions |
| US3161520A (en) * | 1962-12-11 | 1964-12-15 | Gen Aniline & Film Corp | Fog reduction in photographic silver halide emulsions |
| US3617289A (en) * | 1966-12-10 | 1971-11-02 | Fuji Photo Film Co Ltd | Stabilization process for thermally developable light-sensitive elements |
| DE2210369A1 (en) * | 1971-03-04 | 1972-09-28 | Fuji Photo Film Co. Ltd., Ashigara-Kamigun, Kanagawa (Japan) | Process for the production of photographic images |
| DE2263808A1 (en) * | 1971-12-28 | 1973-07-05 | Fuji Photo Film Co Ltd | LIGHT SENSITIVE SILVER HALOGENIDE MATERIAL |
| US4892812A (en) * | 1983-02-04 | 1990-01-09 | Mitsubishi Paper Mills, Ltd. | Silver halide photosensitive materials |
| US5108884A (en) * | 1990-03-30 | 1992-04-28 | Mitsubishi Paper Mills Limited | Antistatically finished silver halide photographic photosensitive material |
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