US3148987A - Photographic material - Google Patents

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US3148987A
US3148987A US142016A US14201661A US3148987A US 3148987 A US3148987 A US 3148987A US 142016 A US142016 A US 142016A US 14201661 A US14201661 A US 14201661A US 3148987 A US3148987 A US 3148987A
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emulsions
emulsion
compounds
silver
compound
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US142016A
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Willems Jozef Frans
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Gevaert Photo Producten NV
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Gevaert Photo Producten NV
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/34Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/34Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
    • G03C1/346Organic derivatives of bivalent sulfur, selenium or tellurium

Definitions

  • the present invention relates to fog inhibiting compounds and stabilizers for light-sensitive photographic emulsions and also to the use of these compounds in lightsensitive photographic material.
  • the silver image formed after exposure undergoes a degradation, by which is meant a shift and a decrease of intensity of the image tone during the finishing to a visible image e.g. under the influence of ingredients used in the developing bath, the fixing bath,
  • R R R and R represent a hydrogen atom, an alkyl radical, a substituted alkyl radical, an alkaryl radical, a substituted alkarylradical, an aryl radical or a substituted aryl radical; or
  • R and R and also R and R two by two represent the atoms necessary to close a saturated homocyclic nucleus or a substituted saturated homocyclic nucleus
  • I 2 CH These compounds may be prepared according to known methods as e.g. those described by l. D. Christian, J. Org. Chem, 22 (1957), 398; Bucherer and Brandt, I. prakt. Chem., (1934), 129; US. patent specifications 2,785,175 and 2,806,036; C. A. 28, 4383 with reference to Science Repts., Tokyo Bunrika Daigaka, Sect. A. 2, 1-7 (1934), and C. A. 22, 2146.
  • the preparation for the greater part corresponds with able layer such as a gelatin covering layer or to an intermediate layer adjacent to the emulsion layer.
  • the used emulsions may be sensitized according to a usual process. They may be chemically sensitized by little quantities of sulphurous compounds such as allyl isothiocyanate, allyl thiourea, sodium thiosulfate, etc.
  • the emulsions may also be sensitized by means of reducing agents e.g. the tin compounds described in the Belgian patent specifications 493,464 and 568,687, the imino-aminomethane sulphinic acid compounds described in the Belgian patent specification 547,323, and small quantities of noble metal compounds e.g.
  • the emulsion may also be sensitized by means of polyalkylene oxide derivatives e.g. polyethylene oxide, the molecular Weight of which varying between 1000 and 20,000 condensation products of alkylene oxides with aliphatic alcohols or glycols, with cyclic dehydrated products of hexitols, with alkyl substituted phenols, with aliphatic carboxylic acids, with aliphatic amines and diamines, and with aliphatic amides.
  • the condensation products may have a molecular weight of at least 700 and preferably above 1000.
  • these sensitizers evidently may be applied in combination, such as described e.g. in the Belgian patent specification 537,278 and in the British patent specification 727,982.
  • these compounds may be applied in optically sensitized emulsions as Well as in non-optically sensitized emulsions.
  • these compounds may also be used in combination with other known stabilizers, e.g. 7-hydroxy-S-alkyl-s-triazolo(2,3-a)pyrimidines e.g. in high-sensitive emulsions containing a development activator of the polyoxyalkylene type.
  • stabilizers e.g. 7-hydroxy-S-alkyl-s-triazolo(2,3-a)pyrimidines e.g. in high-sensitive emulsions containing a development activator of the polyoxyalkylene type.
  • the compounds according to this invention may be applied to all kinds of emulsions such as silver bromide emulsions containing a considerable amount of silver iodide, silver bromide emulsions, silver bromide containing silver chloride emulsions, and silver chloride emulsions, thus in all the usual negative and positive kinds of photographic films and papers.
  • the compounds according to this invention are very efiicient as antibronzing-agents.
  • the quantity of stabilizers may vary according to the kind of the used silver halide or a mixture thereof, the degree of ripening, the presence or the absence of other emulsion additives such as colour couplers, optical bleach- 7 ing agents, anti-oxidation agents, substances influencing the image-tone, etc. Generally the quantity of stabilizer varies between 0.001 and 0.35 g. per mol of silver halide. In some circumstances, however, e.g. in order to achieve determined effects, larger amounts may be used.
  • Example 1 To different samples of the same high-sensitive silver bromo-iodide emulsion (about 3.5% of iodide), amounts of stabilizers are added as indicated in the following table. After chemical ripening the emulsion samples are coated onto strips of a support and dried.
  • These compounds are active not only as stabilizers or as anti-fogging agents, but they also improve the image tone of the developed image, especially in the case the photographic material is hot-glazed. Generally the image thus obtained possesses a bluish black tone without showing, however, a metallic gloss.
  • Example 2 By replacing in the emulsion of Example 2, 1.5 g. of compound 1 by 3.5 g. of compound 2 and treating as in that example, the same results are obtained.
  • Example 4 To a silver chloro-bromide emulsion (35% of chloride) suitable for enlarging negatives, 0.7 g. of the compound 3 is added per mol of silver halide. The emulsion is coated onto a paper support.
  • a silver image is obtained possessing a bluish black image tone without showingany metal gloss or bronzy decoloration. If the emulsion does not contain the above compound, the image tone is more bronze-coloured and after hot-glazing, the silver shows a metallic gloss.
  • Example 5 By replacing in the emulsion of Example 4, 0.7 g. of compound 3 by 2 g. of compound 1 and treating in the same way as in Example 2, identical results are obtained.
  • Photographiclight-sensitive material comprising a 7 silver halide emulsion layer and containing in at least one of its water-permeable layers an imidazolidine-4-thione of the formula:
  • R1 R1 t-e t-r HN NH HN N 5 6 wherein each of R R R and R is a member selected of its water-permeable layers an imidazolidine-4-thione of from the group consisting of a hydrogen atom, an the formula alkyl group and an aryl group.
  • R1 R1 2.
  • Photographic light-sensitive material comprising a R R 5 2 l silver halide emulsion layer and containing m at least one 5 ⁇ L I ll of its water-permeable layers an imidazolidine-4-thione of HN NH the formula: -Y Y wherein each of R and R is a member selected from the group consisting of a hydrogen atom, an alkyl group I T i HN NH HN N and an aryl group, and
  • Y represents the necessary atoms to close a saturated cycloaliphatic ring.
  • Photographic light-Sensitive material Comprising a Futaki et al.: Photographic Science and Engineering
  • silver halide emulsion layer and containing in at least one 20 vol. 4, No. 5, pages 257-263, September-October 1960.

Description

United States Patent 3,148,987 PHQTOGRAPHIC MATERIAL Jozef Frans Willems, Wilrijk-Antwerp, Belgium, assignor to Gevaert Photo-Producten N.V., Mortsel, Belgium, a Belgian company No Drawing. Filed Oct. 2, 1961, Ser. No. 142,016
' 3 Claims. (Cl. 96-10?) The present invention relates to fog inhibiting compounds and stabilizers for light-sensitive photographic emulsions and also to the use of these compounds in lightsensitive photographic material.
It is known that light-sensitive photographic emulsions, on storage in a place of a high temperature and a high relative humidity or wherein these materials come into contact with some substances such as hydrogen sulphide, hydrogen peroxide vapours or reducing agents, tend to lose their sensitivity and become spontaneously developable without any preliminary exposure. This phenomenon is called chemical fog as to diiferentiate it from the light fog due to an undesired exposure. The fog formation depends on the emulsion type and is directly proportional to the age, the temperature and the relative humidity on storage.
It is also known that the silver image formed after exposure undergoes a degradation, by which is meant a shift and a decrease of intensity of the image tone during the finishing to a visible image e.g. under the influence of ingredients used in the developing bath, the fixing bath,
The greater part of these compounds, however, presents the draw-back of being only active within well definite limits and of usually exerting a strong desensitizing action onto the emulsion.
It has now been found that the imidazolidine-4-thiones and their tautomers corresponding to the following general formula wherein Each of R R R and R (equal or different) represents a hydrogen atom, an alkyl radical, a substituted alkyl radical, an alkaryl radical, a substituted alkarylradical, an aryl radical or a substituted aryl radical; or
R and R and also R and R two by two represent the atoms necessary to close a saturated homocyclic nucleus or a substituted saturated homocyclic nucleus,
are effective anti-bronzing agents and exert a stabilizing and a fog-inhibiting action onto light-sensitive photographic emulsions without impairing their sensitivity.
Some compounds according to the present invention 3,148,538? Patented Sept. 15, 1964 Ice which appeared from the experiments to give particularly good results are identified hereinafter:
CO=S
I 2 CH These compounds may be prepared according to known methods as e.g. those described by l. D. Christian, J. Org. Chem, 22 (1957), 398; Bucherer and Brandt, I. prakt. Chem., (1934), 129; US. patent specifications 2,785,175 and 2,806,036; C. A. 28, 4383 with reference to Science Repts., Tokyo Bunrika Daigaka, Sect. A. 2, 1-7 (1934), and C. A. 22, 2146.
The preparation for the greater part corresponds with able layer such as a gelatin covering layer or to an intermediate layer adjacent to the emulsion layer. The used emulsions may be sensitized according to a usual process. They may be chemically sensitized by little quantities of sulphurous compounds such as allyl isothiocyanate, allyl thiourea, sodium thiosulfate, etc. The emulsions may also be sensitized by means of reducing agents e.g. the tin compounds described in the Belgian patent specifications 493,464 and 568,687, the imino-aminomethane sulphinic acid compounds described in the Belgian patent specification 547,323, and small quantities of noble metal compounds e.g. of gold, platinum, palladium, iridium, ruthenium and rhodium. The emulsion may also be sensitized by means of polyalkylene oxide derivatives e.g. polyethylene oxide, the molecular Weight of which varying between 1000 and 20,000 condensation products of alkylene oxides with aliphatic alcohols or glycols, with cyclic dehydrated products of hexitols, with alkyl substituted phenols, with aliphatic carboxylic acids, with aliphatic amines and diamines, and with aliphatic amides. The condensation products may have a molecular weight of at least 700 and preferably above 1000. v
In order to obtain well defined efiects, these sensitizers evidently may be applied in combination, such as described e.g. in the Belgian patent specification 537,278 and in the British patent specification 727,982.
Further these compounds may be applied in optically sensitized emulsions as Well as in non-optically sensitized emulsions.
In order to obtain Well defined effects, these compounds may also be used in combination with other known stabilizers, e.g. 7-hydroxy-S-alkyl-s-triazolo(2,3-a)pyrimidines e.g. in high-sensitive emulsions containing a development activator of the polyoxyalkylene type.
The compounds according to this invention may be applied to all kinds of emulsions such as silver bromide emulsions containing a considerable amount of silver iodide, silver bromide emulsions, silver bromide containing silver chloride emulsions, and silver chloride emulsions, thus in all the usual negative and positive kinds of photographic films and papers. Especially in emulsions of photographic paper sorts which after development are submitted to high-glossing, the compounds according to this invention are very efiicient as antibronzing-agents.
The quantity of stabilizers may vary according to the kind of the used silver halide or a mixture thereof, the degree of ripening, the presence or the absence of other emulsion additives such as colour couplers, optical bleach- 7 ing agents, anti-oxidation agents, substances influencing the image-tone, etc. Generally the quantity of stabilizer varies between 0.001 and 0.35 g. per mol of silver halide. In some circumstances, however, e.g. in order to achieve determined effects, larger amounts may be used.
The following examples illustrate the invention, Without limiting, however, the scope thereof.
Example 1 To different samples of the same high-sensitive silver bromo-iodide emulsion (about 3.5% of iodide), amounts of stabilizers are added as indicated in the following table. After chemical ripening the emulsion samples are coated onto strips of a support and dried.
After storing these light-sensitive materials in a warm and humid atmosphere they are exposed for 4 sec. and developed for 4 minutes in a solution of the following composition:
G. N-methyl-p-aminophenol hemisulphate 1.5 Hydroquinone 6 Sodium sulphite 100 Sodium carbonate 80 Potassium bromide 2 Ethylenediamine tetracetic acid trisodium salt 1.5
Water to make 1 l.
After further treating this sensitive material in a stop bath, washing and fixing the following comparative results were noted.
Fog value Conoentra- Stabilizer tion in rug/mol of Of freshly After 36 h. After 5 days silverhalide coated of ineubaof incubaemulsion Lion tion 0. 09 0. 34 1. 22 Compound 1 6t] 0. 03 0.06 0. 20 Compound 1.. 0. 04 0. 07 0. 20 Compound 2 30 O. 04 0. 10 0. 73 Oomoound 2 150 O. 03 0. 04 0. 09 Compound 4 25 O. 05 0.13 O. 75 Compound 4 75 0. 02 0.03 0. 12 Compound 5 30 0.04 0.09 I 0.47
These compounds are active not only as stabilizers or as anti-fogging agents, but they also improve the image tone of the developed image, especially in the case the photographic material is hot-glazed. Generally the image thus obtained possesses a bluish black tone without showing, however, a metallic gloss.
Example 2 Example 3 By replacing in the emulsion of Example 2, 1.5 g. of compound 1 by 3.5 g. of compound 2 and treating as in that example, the same results are obtained.
Example 4 To a silver chloro-bromide emulsion (35% of chloride) suitable for enlarging negatives, 0.7 g. of the compound 3 is added per mol of silver halide. The emulsion is coated onto a paper support.
This material is exposed in an exact way and developed for 2 min. in a same solution as described in Example 1.
After further treating the material in a stop-bath, washing, fixing, washing and hot-glazing, a silver image is obtained possessing a bluish black image tone without showingany metal gloss or bronzy decoloration. If the emulsion does not contain the above compound, the image tone is more bronze-coloured and after hot-glazing, the silver shows a metallic gloss.
Example 5 By replacing in the emulsion of Example 4, 0.7 g. of compound 3 by 2 g. of compound 1 and treating in the same way as in Example 2, identical results are obtained.
I claim:
1. Photographiclight-sensitive material comprising a 7 silver halide emulsion layer and containing in at least one of its water-permeable layers an imidazolidine-4-thione of the formula:
R1 R1 t-e t-r HN NH HN N 5 6 wherein each of R R R and R is a member selected of its water-permeable layers an imidazolidine-4-thione of from the group consisting of a hydrogen atom, an the formula alkyl group and an aryl group. R1 R1 2. Photographic light-sensitive material comprising a R R 5 2 l silver halide emulsion layer and containing m at least one 5 \L I ll of its water-permeable layers an imidazolidine-4-thione of HN NH the formula: -Y Y wherein each of R and R is a member selected from the group consisting of a hydrogen atom, an alkyl group I T i HN NH HN N and an aryl group, and
Y represents the necessary atoms to close a saturated cycloaliphatic ring.
19 References Cited in the file of this patent wherein each of X and Y are the necessary atoms to close Bruenner; Photographic S ien and En ineering, vol. 21 Saturat d cycloaliphati r g 4, No. 4, pages 186-495, July-August 1960.
Photographic light-Sensitive material Comprising a Futaki et al.: Photographic Science and Engineering,
silver halide emulsion layer and containing in at least one 20 vol. 4, No. 5, pages 257-263, September-October 1960.

Claims (1)

1. PHOTOGRAPHIC LIGHT-SENSITIVE MATERIAL COMPRISING A SILVER HALIDE EMULSION LAYER AND CONTAINING IN AT LEAST ONE OF ITS WATER-PERMEABLE LAYERS AN IMIDAZOLIDINE-4-THIONE OF THE FORMULA:
US142016A 1961-10-02 1961-10-02 Photographic material Expired - Lifetime US3148987A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3287137A (en) * 1962-09-11 1966-11-22 Eastman Kodak Co Light-developable silver halide emulsions
US3330657A (en) * 1963-10-23 1967-07-11 Polaroid Corp Photographic products and processes utilizing 2, 5-dimercapto-1, 3, 4-thiadiazole as an antifoggant
DE2032049A1 (en) * 1969-06-30 1971-01-14 Ilford Ltd, Ilford, Essex (Groß britannien) Process for the production of developed photographic material

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3287137A (en) * 1962-09-11 1966-11-22 Eastman Kodak Co Light-developable silver halide emulsions
US3330657A (en) * 1963-10-23 1967-07-11 Polaroid Corp Photographic products and processes utilizing 2, 5-dimercapto-1, 3, 4-thiadiazole as an antifoggant
DE2032049A1 (en) * 1969-06-30 1971-01-14 Ilford Ltd, Ilford, Essex (Groß britannien) Process for the production of developed photographic material

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