[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

US3544336A - Phosphate antifoggants for photographic emulsions - Google Patents

Phosphate antifoggants for photographic emulsions Download PDF

Info

Publication number
US3544336A
US3544336A US628829A US3544336DA US3544336A US 3544336 A US3544336 A US 3544336A US 628829 A US628829 A US 628829A US 3544336D A US3544336D A US 3544336DA US 3544336 A US3544336 A US 3544336A
Authority
US
United States
Prior art keywords
phosphate
silver
silver halide
antifoggants
emulsion
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
Application number
US628829A
Inventor
Kirby M Milton
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Application granted granted Critical
Publication of US3544336A publication Critical patent/US3544336A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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

Definitions

  • This invention relates to new and improved antifoggants for photographic elements and to photographic silver halide emulsions containing said antifoggants therein.
  • development fog has been reduced by prior art methods of processing exposed silver halide material in the presence of compounds which restrict development of unexposed silver halide.
  • Such compounds can be incorporated in the silver halide emulsion or in the processing solutions for developing such silver halide emulsions.
  • emulsion antifoggants Although a large number of emulsion antifoggants have been used in the prior art, many of these compounds cause undesirable losses in emulsion speed and contrast while others lack adequate compatibility with the emulsion gelatin.
  • the silver halide emulsion of a photographic element or in a layer contiguous to the silver halide emulsion there is incorporated into the silver halide emulsion of a photographic element or in a layer contiguous to the silver halide emulsion, from about 0.1 to about 5.0 grams, preferably from about 0.5 to about 1.0 gram, per mole of silver in the emulsion of an aryl phosphate, an alkyl phosphate, 3, mixed aryl-alkyl phosphate or mixtures thereof.
  • the phosphate may be added to the emulsion or coated onto the element either as an alcoholic solution or in the form of a fine dispersion in gelatin. Use of the phosphate compound results in control of excessive fog formed on forced development of the silver halide emulsion.
  • R R and R may each be the same or different radicals and are alkyl radicals having up to 10 carbon atoms or mononuclear aryl radicals, either or both of which may or may not be substituted.
  • alkyl radicals having up to 10 carbon atoms or mononuclear aryl radicals, either or both of which may or may not be substituted.
  • examples of such radicals include phenyl, cresyl, ethyl, butyl, 2-ethylhexyl, etc.
  • phosphates falling within the formula include trinonyl phosphate, trioctyl phosphate, chlorophenyl diphenyl phosphate, triphenyl phosphate, tricresyl phosphate, tributyl phosphate, tri(2-ethylhexyl) phosphate, dicresylmethyl phosphate, diphenylbutyl phosphate, etc.
  • the silver halide emulsion of a photographic element containing the antifoggants of this invention can contain conventional addenda such as gelatin plasticizers, coating aids, anti-foggants such as the azaindines and hardeners such as aldehyde hardeners, e.g., formaldehyde, mucochloric acid, glutaraldehyde bis(sodium bi-sulfate), maleic dialdehyde, aziridines, dioxane derivatives and oxypolysaccharides.
  • aldehyde hardeners e.g., formaldehyde, mucochloric acid, glutaraldehyde bis(sodium bi-sulfate), maleic dialdehyde, aziridines, dioxane derivatives and oxypolysaccharides.
  • sensitizing dyes useful in sensitizing such emulsions are described, for example, in US. Pats. 2,526,632 of Brooker and
  • Spectral sensitizers which can be used are the cyanines, merocyanines, complex (trinuclear) cyanines, complex (trinuclear) merocyanines, styryls, and hemicyanines.
  • Developing agents can also be incorporated into the silver halide emulsion if desired or can be contained in a separate underlayer.
  • Various silver salts can be used as the sensitive salt such as silver bromide, silver iodide, silver chloride, or mixed silver halides such as silver chlorobromide or silver bromoiodide.
  • the silver halide emulsion layer of a photographic element containing the antifoggants of the invention can .contain any of the hydrophilic, water-permeable binding materials suitable for this purpose. Suitable materials include gelatin, colloidal albumin, polyvinyl compounds, cellulose derivatives, acrylamide polymers, etc. Mixtures of these binding agents can also be used.
  • the binding agents for the emulsion layer of the photographic element can also contain dispersed polymerized vinyl compounds. Such compounds are disclosed, for example, in US. Pats. 3,142,568 of Nottorf issued July 28, 1964; 3,193,386 of White issued July 6, 1965; 3,062,674 of Houck, Smith and Yudelson issued Nov.
  • the silver halide emulsion of a photographic element containing the antifoggants of the invention can be coated on a wide variety of supports.
  • Typical supports are cellulose nitrate film, cellulose ester film, polyvinyl acetal film, polystyrene film, poly(ethylene terephthalate) film and related films or resinous materials as well as glass, paper, metal and the like.
  • Supports such as paper which are coated with a-olefin polymers, particularly polymers of a-olefins containing two or more carbon atoms, as exemplified by polyethylene, polypropylene, ethylenebutene copolymers and the like can also be employed.
  • the speed of photographic emulsions containing the antifoggants of the invention can be further increased by including in the emulsions a variety of hydrophilic colloids such as carboxymethyl protein of the type described in US. Pat. 3,011,890 of Gates, Jr., Miller and Koller issued Dec. 5, 1961, and polysaccharides of the type described in Canadian Pat. 635,206 of Koller and Russell issued Jan. 23, 1962.
  • hydrophilic colloids such as carboxymethyl protein of the type described in US. Pat. 3,011,890 of Gates, Jr., Miller and Koller issued Dec. 5, 1961, and polysaccharides of the type described in Canadian Pat. 635,206 of Koller and Russell issued Jan. 23, 1962.
  • Photographic emulsions containing the antifoggants of the instant invention can also contain speed-increasing compounds such as quaternary ammonium compounds, polyethylene glycols or thioethers. Frequently, useful effects can be obtained by adding the aforementioned speedincreasing compounds to the photographic developer solutions instead of, or in addition to, the photographic emuls1ons.
  • speed-increasing compounds such as quaternary ammonium compounds, polyethylene glycols or thioethers.
  • Photographic elements containing the antifoggants of the invention can be used in various kinds of photographic systems. In addition to being useful in X-ray and other nonoptically sensitized systems they can also be used in orthochromatic, panchromatic and infrared sensitive systems.
  • the sensitizing addenda can be added to photographic systems before or after any sensitizing dyes which are used.
  • Silver halide emulsions containing the antifoggants of the invention can be used in color photography for example emulsions containing color-forming couplers or a second layer, while the two layers are inclose proximity to one another.
  • the antifoggants of the invention could also be utilized by incorporating them into a photographic developer, since image formation would still take place in the presence of the antifoggants and they would still perform their antifoggant function.
  • Triphenyl phosphate is added as a one percent alcoholic solution in an amount of 0.5 gram per silver mole to a panchromatically sensitized, medium-speed silver bromoiodide (3.1 mole percent iodide) emulsion.
  • This emulsion and a control are coated on a polyethylene terephthalate support at a silver coverage of 474 milligrams per square foot, exposed on an intensity scale sensitometer and developed in Kodak D-19 developer with the following results:
  • emulsions to be developed by solutions containing couplers or other color-generating materials emulsions of the mixed-packet type such as described in US. Pat. 2,698,794 of Godowsky issued Jan. 4, 1955; in silver dyebleach systems; and emulsions of the mixed-grain type such as described in US. Pat. 2,592,243 of Carroll and Hanson issued Apr. 8, 1952.
  • Silver halide emulsions containing the antifoggants of the invention can be sensitized using any of the wellknown techniques in emulsion making, for example, by digesting with naturally active gelatin or various sulfur, selenium, tellurium compounds and/or gold compounds.
  • the emulsions am also be sensitized with salts of noble metals of Group VIII of the Periodic Table which have an atomic weight greater than 100.
  • Kodak D-19 developer employed in this example has the following composition:
  • Silver halide emulsions containing the antifoggants of the invention can be used in diffusion transfer processes which utilize the undeveloped silver halide in non-image areas of the negative to form a positive by dissolving the undeveloped silver halide and precipitating it on a silver Triphenyl and tricresyl phosphates are added to emulsions, coated and tested as described in Example 1 with the following results:
  • Examples 8 and 9 illustrate that optimum results are obtained at concentrations of about 5 grams or below of phosphate in the photographic emulsion. While higher Fos.timeindeveloper amounts of phosphate may be utilized to control fog,
  • Example 5 12 24 36 5 they have a tendency to decrease the speed obtained. min. in. mm mm EXAMPLE 3 Control 0. 03 0.22 0.38 0. 65 Control plus triphenyl phosphate 0.03 0. 04 0.16 0.30
  • the process of Example 5 1s repeated substltutmg cellulose acetate for the polyethylene terephthalate support
  • the Kodak DK-SO developer used in this example has and using the amounts of triphenyl phosphate indicated the following composition: below with the following results:
  • EXAMPLE 9 EXAMPLE 5 The process of Example 8 is repeated substituting poly- Tl-iphenyl phosphate at 5 gram per mole f silver i ethylene terephthalate for the cellulose acetate support added to a high speed panchromatically sensitized, silver Wlth the followmg results: bromoiodide (6.5 mole percent iodide) emulsion. This emulsion and a control are coated on a polyethylene terephthalate support at a coverage of 515 milligrams silver Time in per square foot. They are developed 1n Kodak D-19 8 mm 36 min developer with the following results: Phosphate,
  • Example 5 The process of Example 5 is repeated substituting cel- 45 lulose acetate for the polyethylene terephthalate support
  • the invention has been described in considerand usmg the phosphates indlcated below w1th the folable detail with reference to certain embodiments therelowing results: of, it will be understood that variations and modifica- Tlme in developer 8min. 24min. 36 min. Phosphate,
  • a photographic silver halide emulsion containing from about 0.1 to about 5.0 grams per mole of-silver in said silver halide emulsion of an aryl phosphate, an alkyl phosphate, a mixed aryl-alkyl phosphate or mixtures thereof.
  • a photographic element comprising a support coated with a silver halide emulsion, said element containing from about 0.1 to about 5.0 grams per mole of silver in said silver halide emulsion of an aryl phosphate, an alkyl phosphate, a mixed aryl-al-kyl phosphate or mixtures thereof.
  • phosphate has the formula wherein R R and R may each be an alkyl radical having up to 10 carbon atoms or a mononuclear aryl radical.

Landscapes

  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Description

United States Patent 3,544,336 PHOSPHATE ANTIFOGGANTS FOR PHOTOGRAPHIC EMULSIONS Kirby M. Milton, Rochester, N. assignor to Eastman Kodak Company, Rochester, N.Y., a corporation of New Jersey N0 Drawing. Filed Apr. 6, 1967, Ser. No. 628,829 Int. Cl. G03c N34 US. Cl. 96-109 16 Claims ABSTRACT OF THE DISCLOSURE A photographic silver halide emulsion or photographic element containing as an antifoggant an aryl, alkyl or mixed alkyl-aryl phosphate.
BACKGROUND OF THE INVENTION Field of the invention This invention relates to new and improved antifoggants for photographic elements and to photographic silver halide emulsions containing said antifoggants therein.
Description of the prior art During development of a silver halide emulsion, small amounts of unexposed silver halide are reduced to metallic silver. This reduction of unexposed silver halide produces an objectionable background fog.
It is often desirable to use developers of high activity to develop photographic films. In addition, certain films such as aerographic and color negative films are often developed for long times even in developers of high activity in order to obtain more information or speed. Kodak D-19 Developer-a high sulfite, high-bromide, Elon-hydroquinone developeris typical of such developers used with black-and-white emulsions whereas paraphenylene diamine-type developers are used with color films. In the past, such developers have often given rise to excessive fog at long development times with certain spectrally sensitized emulsions.
Development fog has been reduced by prior art methods of processing exposed silver halide material in the presence of compounds which restrict development of unexposed silver halide. Such compounds can be incorporated in the silver halide emulsion or in the processing solutions for developing such silver halide emulsions. Although a large number of emulsion antifoggants have been used in the prior art, many of these compounds cause undesirable losses in emulsion speed and contrast while others lack adequate compatibility with the emulsion gelatin.
SUMMARY OF THE INVENTION According to this invention, there is incorporated into the silver halide emulsion of a photographic element or in a layer contiguous to the silver halide emulsion, from about 0.1 to about 5.0 grams, preferably from about 0.5 to about 1.0 gram, per mole of silver in the emulsion of an aryl phosphate, an alkyl phosphate, 3, mixed aryl-alkyl phosphate or mixtures thereof. The phosphate may be added to the emulsion or coated onto the element either as an alcoholic solution or in the form of a fine dispersion in gelatin. Use of the phosphate compound results in control of excessive fog formed on forced development of the silver halide emulsion.
ice
DESCRIPTION OF THE PREFERRED EMBODIMENTS Preferred fog stabilizing compounds of this invention have the formula wherein R R and R may each be the same or different radicals and are alkyl radicals having up to 10 carbon atoms or mononuclear aryl radicals, either or both of which may or may not be substituted. Examples of such radicals include phenyl, cresyl, ethyl, butyl, 2-ethylhexyl, etc. Examples of phosphates falling within the formula include trinonyl phosphate, trioctyl phosphate, chlorophenyl diphenyl phosphate, triphenyl phosphate, tricresyl phosphate, tributyl phosphate, tri(2-ethylhexyl) phosphate, dicresylmethyl phosphate, diphenylbutyl phosphate, etc.
The silver halide emulsion of a photographic element containing the antifoggants of this invention can contain conventional addenda such as gelatin plasticizers, coating aids, anti-foggants such as the azaindines and hardeners such as aldehyde hardeners, e.g., formaldehyde, mucochloric acid, glutaraldehyde bis(sodium bi-sulfate), maleic dialdehyde, aziridines, dioxane derivatives and oxypolysaccharides. sensitizing dyes useful in sensitizing such emulsions are described, for example, in US. Pats. 2,526,632 of Brooker and White issued Oct. 24, 1950, and 2,503,776 of Sprague issued Apr. 11, 1950. Spectral sensitizers which can be used are the cyanines, merocyanines, complex (trinuclear) cyanines, complex (trinuclear) merocyanines, styryls, and hemicyanines. Developing agents can also be incorporated into the silver halide emulsion if desired or can be contained in a separate underlayer. Various silver salts can be used as the sensitive salt such as silver bromide, silver iodide, silver chloride, or mixed silver halides such as silver chlorobromide or silver bromoiodide.
The silver halide emulsion layer of a photographic element containing the antifoggants of the invention can .contain any of the hydrophilic, water-permeable binding materials suitable for this purpose. Suitable materials include gelatin, colloidal albumin, polyvinyl compounds, cellulose derivatives, acrylamide polymers, etc. Mixtures of these binding agents can also be used. The binding agents for the emulsion layer of the photographic element can also contain dispersed polymerized vinyl compounds. Such compounds are disclosed, for example, in US. Pats. 3,142,568 of Nottorf issued July 28, 1964; 3,193,386 of White issued July 6, 1965; 3,062,674 of Houck, Smith and Yudelson issued Nov. 6, 1962; and 3,220,844 of Houck, Smith and Yudelson issued Nov. 30, 1965; and include the water-insoluble polymers of alkyl acrylates and methacrylates, acrylic acid, sulfoalkyl acrylates or methacrylates and the like.
The silver halide emulsion of a photographic element containing the antifoggants of the invention can be coated on a wide variety of supports. Typical supports are cellulose nitrate film, cellulose ester film, polyvinyl acetal film, polystyrene film, poly(ethylene terephthalate) film and related films or resinous materials as well as glass, paper, metal and the like. Supports such as paper which are coated with a-olefin polymers, particularly polymers of a-olefins containing two or more carbon atoms, as exemplified by polyethylene, polypropylene, ethylenebutene copolymers and the like can also be employed.
The speed of photographic emulsions containing the antifoggants of the invention can be further increased by including in the emulsions a variety of hydrophilic colloids such as carboxymethyl protein of the type described in US. Pat. 3,011,890 of Gates, Jr., Miller and Koller issued Dec. 5, 1961, and polysaccharides of the type described in Canadian Pat. 635,206 of Koller and Russell issued Jan. 23, 1962.
Photographic emulsions containing the antifoggants of the instant invention can also contain speed-increasing compounds such as quaternary ammonium compounds, polyethylene glycols or thioethers. Frequently, useful effects can be obtained by adding the aforementioned speedincreasing compounds to the photographic developer solutions instead of, or in addition to, the photographic emuls1ons.
Photographic elements containing the antifoggants of the invention can be used in various kinds of photographic systems. In addition to being useful in X-ray and other nonoptically sensitized systems they can also be used in orthochromatic, panchromatic and infrared sensitive systems. The sensitizing addenda can be added to photographic systems before or after any sensitizing dyes which are used.
Silver halide emulsions containing the antifoggants of the invention can be used in color photography for example emulsions containing color-forming couplers or a second layer, while the two layers are inclose proximity to one another.
While it is preferred to utilize the antifoggants of the invention by incorporating them directly into a photographic element, the antifoggants could also be utilized by incorporating them into a photographic developer, since image formation would still take place in the presence of the antifoggants and they would still perform their antifoggant function.
The invention can be further illustrated by the following examples or preferred embodiments thereof, although it will be understood that these examples are included merely for purposes of illustration and are not intended to limit the scope of the invention,
EXAMPLE 1 Triphenyl phosphate is added as a one percent alcoholic solution in an amount of 0.5 gram per silver mole to a panchromatically sensitized, medium-speed silver bromoiodide (3.1 mole percent iodide) emulsion. This emulsion and a control are coated on a polyethylene terephthalate support at a silver coverage of 474 milligrams per square foot, exposed on an intensity scale sensitometer and developed in Kodak D-19 developer with the following results:
emulsions to be developed by solutions containing couplers or other color-generating materials, emulsions of the mixed-packet type such as described in US. Pat. 2,698,794 of Godowsky issued Jan. 4, 1955; in silver dyebleach systems; and emulsions of the mixed-grain type such as described in US. Pat. 2,592,243 of Carroll and Hanson issued Apr. 8, 1952.
Silver halide emulsions containing the antifoggants of the invention can be sensitized using any of the wellknown techniques in emulsion making, for example, by digesting with naturally active gelatin or various sulfur, selenium, tellurium compounds and/or gold compounds. The emulsions am also be sensitized with salts of noble metals of Group VIII of the Periodic Table which have an atomic weight greater than 100.
Kodak D-19 developer employed in this example has the following composition:
Water to make 1 liter.
EXAMPLE 2 Coatings similar to those in Example 1 are made on a cellulose triacetate support. They are similarly evaluated with the following results:
Silver halide emulsions containing the antifoggants of the invention can be used in diffusion transfer processes which utilize the undeveloped silver halide in non-image areas of the negative to form a positive by dissolving the undeveloped silver halide and precipitating it on a silver Triphenyl and tricresyl phosphates are added to emulsions, coated and tested as described in Example 1 with the following results:
Relative speed, time in PhosI/flfiate, Fog, time in developer- Developer S V81 8 mole a min. 20 min. 36 min. 3 min. 20 min. 36 min.
Control 0. 13 0. 67 1.46 100 174 174 Control plus Triphenyl phosphate 0. 5 0. 08 0. 42 0. 97 82 155 166 Do 1. 0 0. 07 0. 35 0. 83 78 143 166 0.5 0. 0s 0. 45 1.09 91 166 166 1. 0 0. 06 0. 39 0. 93 87 155 166 layer in close proximity to the original silver halide emulsion layer. Such processes are described in US. Pats. EXAMPLE 4 2,352,014 of Rott issued June 20, 1944; 2,543,181 of Land issued Feb. 27, 1951; and 3,020,155 of Yackel, Yutzy, Foster and Rasch issued Feb. 6, 1962. The emulsions can also be used in diffusion transfer color processes which utilize a diffusion transfer of an imagewise distribution of developer, coupler or dye, from a light-sensitive layer to silver per square foot. They are developed in Kodak DKO developer with the following results:
Examples 8 and 9 illustrate that optimum results are obtained at concentrations of about 5 grams or below of phosphate in the photographic emulsion. While higher Fos.timeindeveloper amounts of phosphate may be utilized to control fog,
5 12 24 36 5 they have a tendency to decrease the speed obtained. min. in. mm mm EXAMPLE 3 Control 0. 03 0.22 0.38 0. 65 Control plus triphenyl phosphate 0.03 0. 04 0.16 0.30 The process of Example 5 1s repeated substltutmg cellulose acetate for the polyethylene terephthalate support The Kodak DK-SO developer used in this example has and using the amounts of triphenyl phosphate indicated the following composition: below with the following results:
Grams N-methyl-p-aminophenol sulfate 2.5 Hvdroquinone 2.5
Tlmeln develo er S0d1um sulfite, des1ccated 30.0 p Sodium metaborate 10.0 Phosphate 3mm Potassium bromide 0.5 g. per Relative Relative Water to make 1 liter. silver mole speed Fog speed Fog Samples of the films of this example are also developed 5; 115 50 in Kodak Dl9 developer with the following results: p e v phosphate 0. 5 100 0.22 126 0. 40 Do 1.0 95 0.20 115 0.34 2.0 87 0.18 100 0. 2s Fog, time in developer- 4. 0 83 0. 16 91 0. 24 8.0 83 0.12 87 0.13 5 12 24 36 16.0 30 0.12 87 0.16 min. min. min. min.
Control 0.06 0.11 0.55 0. 04 25 Control plus triphenyl phosphate 0.06 0.07 0. 20 0.36
EXAMPLE 9 EXAMPLE 5 The process of Example 8 is repeated substituting poly- Tl-iphenyl phosphate at 5 gram per mole f silver i ethylene terephthalate for the cellulose acetate support added to a high speed panchromatically sensitized, silver Wlth the followmg results: bromoiodide (6.5 mole percent iodide) emulsion. This emulsion and a control are coated on a polyethylene terephthalate support at a coverage of 515 milligrams silver Time in per square foot. They are developed 1n Kodak D-19 8 mm 36 min developer with the following results: Phosphate,
g. per Relative Relative Fog timein developer silver mole speed Fog speed Fog Control 100 0. 129 0. s2 5 Control plus tri- 40 pheuyl phosphate 0.5 105 0.29 115 0.54 Control 0.01 0.01 0.21 0.42 D 5 2g 3; 333 Control plus tnphenyl phosphate 0.03 0. 08 0.15 0.23 40 76 Q15 80 Q22 8.0 73 0.12 30 0.16 16.0 69 0.12 76 0.16 EXAMPLE 6 The process of Example 5 is repeated substituting cel- 45 lulose acetate for the polyethylene terephthalate support Although the invention has been described in considerand usmg the phosphates indlcated below w1th the folable detail with reference to certain embodiments therelowing results: of, it will be understood that variations and modifica- Tlme in developer 8min. 24min. 36 min. Phosphate,
g. per Relative Relative Relative silver mole speed Fog speed Fog speed Fog (nnh'nl 0.03 155 0.09 170 0.23 Control plus triphenyl phosphate 1.0 94 0.03 148 0.08 170 0.18 Control plus tributyl phosphate 1.0 97 0.03 155 0. 08 174 0.19 Control plus tri(2-ethy1hexyl) phosphate 1.0 0.02 159 0.09 182 0.21
EXAMPLE7 tions can be effected without departing from the spirit The process of Example 5 is repeated using the phos and scope of the invention as described hereinabove and as defined in the appended claims. phates mdlcated below with the followmg results.
Timeindeveloper 8min. 24min. 36 min. Phosphate,
g. per Relative Relative Relative silver mole speed Fog speed Fog speed Fog Conn-01- 100 0.04 151 0.14 166 0.33 Control plus tributyl phosphate 1.0 91 0.02 155 0.10 162 0.24 Control plus tn(2'ethy1l1exyl) phosphate. 1.0 95 0.03 148 0.12 162 0.29
I claim:
1. A photographic silver halide emulsion containing from about 0.1 to about 5.0 grams per mole of-silver in said silver halide emulsion of an aryl phosphate, an alkyl phosphate, a mixed aryl-alkyl phosphate or mixtures thereof.
2. The emulsion of claim 1 wherein said phosphate has the formula wherein R R and R may each be an alkyl radical having up to carbon atoms or a mononuclear aryl radical.
3. The emulsion of claim 1 wherein said phosphate is present in an amount of from about 0.5 gram to about 1.0 gram per mole of silver in said silver halide emulsion.
4. The emulsion of claim 1 wherein said phosphate is triphenyl phosphate.
5. The emulsion of claim 1 wherein said phosphate is tricresyl phosphate.
6. The emulsion of claim 1 wherein said phosphate is tributyl phosphate.
7. The emulsion of claim 1 wherein said phosphate is tri(Z-ethylhexyl) phosphate.
8. A photographic element comprising a support coated with a silver halide emulsion, said element containing from about 0.1 to about 5.0 grams per mole of silver in said silver halide emulsion of an aryl phosphate, an alkyl phosphate, a mixed aryl-al-kyl phosphate or mixtures thereof.
i 9. The photographic element of claim 8 wherein said phosphate has the formula wherein R R and R may each be an alkyl radical having up to 10 carbon atoms or a mononuclear aryl radical.
10. The photographic element of claim 8 wherein said phosphate ispresent in a layer contiguous to said silver halide emulsion.
11. The photographic element of claim 8 wherein said phosphate is present in said silver halide emulsion.
12. The photographic element of claim 8 wherein said phosphate is present in an amount of from about 0.5 to about 1.0 gram per mole of silver in said silver halide emulsion.
13. The photographic element of claim 8 wherein said phosphate is triphenyl phosphate. 7 l
14. The photographic element of claim 8 wherein said phosphate is tricresyl phosphate.
15. The photographic element of claim 8 wherein said phosphate is tributyl phosphate.
16. The photographic element of claim 8 wherein said phosphate is tri(Z-ethylhexyl) phosphate.
References Cited UNITED STATES PATENTS 3,057,721 10/ 1962 Cowdan et a1 96-109 X OTHER REFERENCES Abstract of Gevaert Photo-Producten patent Belg. 609,497 in Chemical Abstracts vol. 58, p. 7542 G, 1963.
NORMAN G. TORCHIN, Primary Examiner R. E. FICHTER, Assistant Examiner
US628829A 1967-04-06 1967-04-06 Phosphate antifoggants for photographic emulsions Expired - Lifetime US3544336A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US62882967A 1967-04-06 1967-04-06

Publications (1)

Publication Number Publication Date
US3544336A true US3544336A (en) 1970-12-01

Family

ID=24520479

Family Applications (1)

Application Number Title Priority Date Filing Date
US628829A Expired - Lifetime US3544336A (en) 1967-04-06 1967-04-06 Phosphate antifoggants for photographic emulsions

Country Status (4)

Country Link
US (1) US3544336A (en)
BE (1) BE712877A (en)
FR (1) FR1557552A (en)
GB (1) GB1217051A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4326022A (en) * 1979-12-07 1982-04-20 Konishiroku Photo Industry Co., Ltd. Photographic material containing a high boiling solvent
US4353979A (en) * 1979-07-25 1982-10-12 Konishiroku Photo Industry Co., Ltd. Light-sensitive silver halide photographic materials
US4980275A (en) * 1988-04-13 1990-12-25 Eastman Kodak Company Photographic material and process comprising a dye stabilizer
US6696237B1 (en) * 1999-10-26 2004-02-24 Fuji Photo Film Co., Ltd. Photothermographic material
US20040115572A1 (en) * 2002-12-03 2004-06-17 Yoshihisa Tsukada Photothermographic material
US20040126722A1 (en) * 2000-10-26 2004-07-01 Yasuhiro Yoshioka Photothermographic material
US6783927B2 (en) * 2000-07-07 2004-08-31 Fuji Photo Film, Co., Ltd. Photothermographic material
US20060199115A1 (en) * 2001-01-30 2006-09-07 Hajime Nakagawa Photothermographic material and image forming method
US20060204908A1 (en) * 2002-12-03 2006-09-14 Hajime Nakagawa Photothermographic material
US20070099132A1 (en) * 2000-09-18 2007-05-03 Hajime Nakagawa Photothermographic material
US20070122755A1 (en) * 1999-10-26 2007-05-31 Yasuhiro Yoshioka Heat developable photosensitive material including a combination of specified reducing agents

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3057721A (en) * 1959-12-28 1962-10-09 Eastman Kodak Co Photographic colloid transfer process

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3057721A (en) * 1959-12-28 1962-10-09 Eastman Kodak Co Photographic colloid transfer process

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4353979A (en) * 1979-07-25 1982-10-12 Konishiroku Photo Industry Co., Ltd. Light-sensitive silver halide photographic materials
US4326022A (en) * 1979-12-07 1982-04-20 Konishiroku Photo Industry Co., Ltd. Photographic material containing a high boiling solvent
US4980275A (en) * 1988-04-13 1990-12-25 Eastman Kodak Company Photographic material and process comprising a dye stabilizer
US6696237B1 (en) * 1999-10-26 2004-02-24 Fuji Photo Film Co., Ltd. Photothermographic material
US20040038163A1 (en) * 1999-10-26 2004-02-26 Fuji Photo Film Co., Ltd. Photothermographic material
US20070122755A1 (en) * 1999-10-26 2007-05-31 Yasuhiro Yoshioka Heat developable photosensitive material including a combination of specified reducing agents
US6783927B2 (en) * 2000-07-07 2004-08-31 Fuji Photo Film, Co., Ltd. Photothermographic material
US20070099132A1 (en) * 2000-09-18 2007-05-03 Hajime Nakagawa Photothermographic material
US20040126722A1 (en) * 2000-10-26 2004-07-01 Yasuhiro Yoshioka Photothermographic material
US20070134603A9 (en) * 2000-10-26 2007-06-14 Yasuhiro Yoshioka Photothermographic material
US20060199115A1 (en) * 2001-01-30 2006-09-07 Hajime Nakagawa Photothermographic material and image forming method
US20060204908A1 (en) * 2002-12-03 2006-09-14 Hajime Nakagawa Photothermographic material
US20040115572A1 (en) * 2002-12-03 2004-06-17 Yoshihisa Tsukada Photothermographic material
US7381520B2 (en) 2002-12-03 2008-06-03 Fujifilm Corporation Photothermographic material

Also Published As

Publication number Publication date
BE712877A (en) 1968-07-31
FR1557552A (en) 1969-02-14
GB1217051A (en) 1970-12-23

Similar Documents

Publication Publication Date Title
US3297446A (en) Synergistic sensitization of photographic systems with labile selenium and a noble metal
US3220839A (en) Photographic emulsions containing isothiourea derivatives
US3297447A (en) Stabilization of synergistically sensitized photographic systems
US2886437A (en) Photographic emulsions sensitized with alkylene oxide polymers and quaternary ammonium compounds
US3930867A (en) Macrocyclic polyamines as sensitizers for silver halide emulsions
US3656955A (en) Silver halide emulsion sensitized with pentathiepane
US3547638A (en) N,n-disubstituted amino-methylthiocarboxylic acids and use thereof as antifoggants in photographic emulsions
US3598598A (en) Fog stabilizers for photographic emulsions
US3544336A (en) Phosphate antifoggants for photographic emulsions
US3499761A (en) Silver halide emulsions containing alkyl esters of benzimidazole carbamic acid antifogging agents
US3442653A (en) Sensitized silver halide systems with activated nonlabile selenium compounds
US3519426A (en) Preparation of silver halide emulsions having high covering power
US3488709A (en) Stabilizing silver halide emulsions with cadmium bromide
US3576638A (en) High molecular weight, long chain tetrazole-containing polymers for antifogging use in photographic elements
US2772164A (en) Photographic silver halide emulsions containing 1-thia-3, 5, 7-triazaindenes
US3271158A (en) Photographic silver halide emulsions having high wet density retention
US3408197A (en) Synergistic sensitization of silver halide emulsions with labile selenium formed in situ
US3598600A (en) Photographic compositions and elements containing polymeric imidazoles
US3785822A (en) Photographic emulsions and developers containing 2-mercapto heterocyclic compounds
US3706562A (en) Photographic materials and processes for developing photographic compositions
US3420670A (en) Stabilization of synergistically sensitized photographic systems
US3060028A (en) Stabilized photographic silver halide emulsions containing iodine complexes of poly-n-vinyl-2-oxazolidinones
US3408196A (en) Sensitization of silver halide emulsion with labile selenium formed in situ
US3573049A (en) Photographic materials and processes for developing photographic compositions having a zwitterionic and anionic elements
US3607278A (en) Photographic elements containing fogged and unfogged silver halide grains and a slow silver halide emulsion layer