US2708161A - Parabanic acid stabilizer for photographic emulsions sensitized with alkylene oxide polymers - Google Patents

Parabanic acid stabilizer for photographic emulsions sensitized with alkylene oxide polymers Download PDF

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US2708161A
US2708161A US426542A US42654254A US2708161A US 2708161 A US2708161 A US 2708161A US 426542 A US426542 A US 426542A US 42654254 A US42654254 A US 42654254A US 2708161 A US2708161 A US 2708161A
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alkylene oxide
emulsions
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fog
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Jean E Jones
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Eastman Kodak Co
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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

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  • This invention relates to fog inhibiting agents and stabilizers for photographic emulsions and to photographic emulsions containing them.
  • Fog depends both on the emulsionand the conditions of development; for a given emulsion it increases with the degree of development. With constant development conditions, it tends to increase with time, temperature and relative humidity of storage conditions; it is common practice to make accelerated tests of the stability of photographic emulsions by storage at increased temperature or humidity, or both. It is, of course, desirable to have emulsions as stable as possible under the conditions of high temperature and humidity which may occur in tropical climates, for example. Fog usually appears over the whole area of the sensitive coating, but when severe, it frequently is non-uniform. Fog may also be caused by exposure to chemicals, for example, hydrogen sulfide and other reactive sulfur compounds, hydrogen peroxide vapor, and strongly reducing materials. While antifoggants and stabilizers may protect, to some extent, against such effects, it is normally understood that an antifoggant protects against spontaneous growth of fog during prolonged storage or storage at high temperatures and humidities, or during development to maximum contrast and speed, or both.
  • a further object isto provide a means for reducing the fog produced upon keeping of emulsions so sensitized, especially emulsions stored under tropical I or other adverse conditions.
  • 'A still further object isjtoj provide a means for stabilizing the speed and contrast of emulsions so sensitized. 'Other objects will appear from the following description of my invention.
  • alkylene oxide polymers parabanic acid as a stabilizing and fog inhibiting agent.
  • Parabanic acid also known as oxalylurea and imidazoletrione, has the structure 0 0 r m-( O
  • the alkylene oxide polymers used to sensitize the emulsions may be of various types.
  • the alkylene oxides from which the polymers are derived contain from 2 to 4 carbon atoms, e. g., ethylene oxide, propylene oxide, and
  • butylene oxide The preparation of polymers from these compounds is described in Ellis, The Chemistry of Synthetic Resins (1935), pages 990 to 994. These compounds are also referred to as polyalkylene glycols and their use as sensitizers for silver halide emulsions is described in U. S. Patents 2,423,549 and 2,441,389.
  • alkylene oxides may also be used to sensitize the silver halide emulsions, e. g., condensation products of alkylene oxide with glycols, such as those having from 8 to 18 carbon atoms as described in U. S. Patent 2,240,472 and British Patent 443,559, as well as condensation products of alkylene oxides with aliphatic alcohols, aliphatic acids and aliphatic amines, that is, polyalkylene ethers, esters and amides, the preparation of which is described in U. S. Patent 1,970,578, condensation products of alkylene oxides with phenols, also described in U. S. Patent 1,970,578, and condensation products of alkylene oxides with hexitol ring dehydration products, as described in U. S. Patent 2,400,532.
  • condensation products of alkylene oxide with glycols such as those having from 8 to 18 carbon atoms as described in U. S. Patent 2,240,472 and British Patent 443,559
  • polyalkylene oxide or derivative of alkylene oxide should have a molecular weight of at least 300.
  • Condensation products of ethylene oxide with long chain alcohols should have a molecular weight of about 700; other derivatives may have a molecular weight of 1500 to 4000 or more.
  • the principal purpose of my invention is to provide means for maintaining the sensitivity and fog of silver halide emulsions at or close to initial optimum values under conditions of high temperature or high humidity, or both.
  • the fog inhibitor which I propose to use is added to the emulsion at any stage during the process of manufacture prior to coating the emulsion.
  • the parabanic acid fog inhibitor may be added to the emulsion in solution in any convenient solvent not injurious to the emulsion such as lower alcohols.
  • Parabanic acid added at the levels needed for good antifoggant action lowers the pH of the emulsion to a considerable extent (approximately 4.8). Neutralization of the acid before addition to the emulsion, or of the emulsion after addition, diminishes the antifoggant efiect somewhat, but does not eliminate it completely.
  • An additional purpose of my invention is to provide an antifoggant which may be used with emulsions sensitized with alkylene oxide polymers and which does not interfere with the action of certain gelatin hardening agents.
  • Parabanic acid does not alfect the hardening actionof mu'cochloric acid, a-hydroxyadipaldehyde or 1,5-bis- (methane sulfonoxy)-pentane (Allen and Laakso U. S- application Serial No. 259,511, filed December 1, 1951). It does interfere somewhat with the hardening action of formaldehyde and glyoxal, although it does not prevent complete hardening in the case of formaldehyde.
  • the preparation of silver halide emulsions involves three separate operations: (1) the emulsification and digestion or ripening of the silver halide, (2) the freeing of the emulsion from aqueous soluble salts usually by washing, (3) the second digestion or after-ripening to obtain increased sensitivity (Mees, The Theory of the Photographic Process, 1942, page 3).
  • the fog inhibiting agents may be added at any stage, preferably after the final digestion.
  • the photographic emulsions which I use are of the developing-out type and .best results have been obtained with gelatino-silver bromoiodide emulsions. However, emulsions of varying halide content may .be used.
  • the emulsions may be chemically sensitized by any of the accepted procedures, in addition to or in combination with the sensitizing with alkylene oxide polymers.
  • the emulsions may be digested with naturally active gelatin, or sulfur compounds may be added such as those described in Sheppard U. S. Patent 1,574,944 and 1,623,499, and Sheppard and Brigham U. S. Patent 2,410,689.
  • the emulsions may also be treated with salts .of the noble metals such as ruthenium, rhodium, palladium, iridium and platinum, all of which belong to group VIII of the periodic table of elements and have an atomic weight greater than 100.
  • Representative compounds are ammonium chloropalladate, potassium chloroplatinate and sodium chloropalladite, which are used for sensitizing in amounts below that which produces any substantial fog inhibition, as described in Smith and Trivelli U. S. Patent 2,448,060, and as antifoggants in higher amounts, as described in Trivelli and Smith U. S. Patents 2,566,245 and 2,5 66,263.
  • the emulsions may also be chemically sensitized with gold salts as described in Waller and Dodd U. S. Patent 2,399,083, or stabilized with gold salts as described in Damschrodcr U. S. Patent 2,597,856 and Yutzy and Leermakers U. S. Patent 2,597,915.
  • Suitable compounds are potassium chloroaurite, potassium aurithiocyanate, potassium chloroaurate, auric trichloride and 2-aurosulfobenzothiazole methochloride.
  • the emulsions may also be chemically sensitized with reducing agents such as stannous salts (Carroll U. S. Patent 2,487,850), polyamines such as diethylene triamine (Lowe and Jones U. S. Patent 2,518,698), polyamines 4 such as spermine (Lowe and Allen U. S. Patent 2,521,925), or bis-(fl-aminoethyl) sulfide and its watersoluble salts (Lowe and Jones U. S. Patent 2,521,926).
  • reducing agents such as stannous salts (Carroll U. S. Patent 2,487,850), polyamines such as diethylene triamine (Lowe and Jones U. S. Patent 2,518,698), polyamines 4 such as spermine (Lowe and Allen U. S. Patent 2,521,925), or bis-(fl-aminoethyl) sulfide and its watersoluble salts (Lowe and Jones U. S. Patent 2,521,926).
  • the emulsions may also be stabilized with the mercury compounds of Allen, Byers and Murray U. S. application Serial No. 319,611, Carroll and Murray U. S. application Serial No. 319,612 and Leubner and Murray U. S. application Serial No. 319,613, all filed November 8, 1952.
  • the sensitizing and stabilizing combinations of polyalkylene oxides and parabanic acid are effective in the presence or absence of optical sensitizing dyes. Since optical sensitizing may affect stability of emulsions with respect to sensitivity, fog and latent image changes, the action of parabanic acid is not completely independent of optical sensitizing or other emulsion variables. I have found, however, that both unsensitized emulsions and emulsions sensitized with cyanine or merocyanine dyes or both, may be treated with polyalkylene oxides and parabanic acid according to my invention.
  • the most useful concentration of parabanic acid in the emulsion is from 1 to 8 or more grams per gram mole of silver halide in the emulsion. These amounts may be used in combination with one or more of the chemical sensitizing and stabilizing agents listed above.
  • the stabilizing action was determined by incubation of the emulsions for a period from 1 to 4 weeks at 100 to 120 F. and constant humidity. Speeds were measured in terms of 30/E where E is the exposure required to produce a density of 0.2 above fog. The results of aging tests are tabulated in the examples below and compare speed, gamma and fog of the emulsions with and without the stabilizing compound.
  • Example I A negative-speed gelatino-silver bromoiodide emulsion was digested with a sulfur compound such as disclosed in Sheppard U. S. Patent 1,574,944 and potassium chloroaurate, and chemically sensitized with about 0.75 gram per gram mole of silver halide, of polyethylene oxide oleyl ether. The emulsion was then panchromatically sensitized. To portions of the emulsion there were added varying amounts of parabanic acid as shown in the following tables. Portions of the emulsions with and without the parabanic acid were coated on cellulose acetate film support, dried, exposed on an Eastman Ib Sensitometer and developed for 5 minutes at 68 F. in a developer of the following formula:
  • Various silver salts may be used as the sensitive salt, such as silver bromide, silver iodide, silver chloride" or mixed silver halides.
  • the parabanic acid and alkylene oxide polymers may be used in emulsions intended .for color photography, for example, emulsions containing color-forming couplers, or emulsions to be developed by solutions containing couplers.
  • the dispersing agents may be gelatin or other colloid such as collodion, albumen, cellulose derivatives or synthetic resins.
  • alkylene glycols consisting of (1) polyalkylene glycols, (2) condensation products of alkylene oxide with glycols, (3) condensationproducts of alkylene oxide with aliphatic compounds. selected from the class consisting of alcohols, acids and amines, (4) condensation products of alkylene oxide with phenols, and (5) condensation products of alkylene oxide with hexitol ring dehydration products, said alkyl- Amount Fresh Test After Incubation Compound per mole,
  • the polyethylene oxide lauric ester (I) of Example 2 was made by condensing 1 mole of lauric acid with approximately 26 moles of ethylene oxide.
  • the polyethylene oxide ether of glucose monolaurate (III), the polyethylene oxide laurylamide compound (IV) and the polyethylene oxide phenyl ether (V) were prepared as described in Carroll U. S. application Serial No. 426,543, filed concurrently herewith.
  • the polyethylene oxide polymers used in the emulsions according to my invention may be prepared either by polymerizing ethylene oxide in the presence of aliphatic acids, aliphatic amines or phenols, or by reacting the polymerized polyethylene oxide with aliphatic acids, acid chlorides, or esters, which produces similar products.
  • the fog inhibitor of my invention may be incorporated in a colloid layer such as a gelatin overcoating layer or interlayer in contact with the emulsion.
  • the fog-inhibiting agents which I have described may be used in various kinds of photographic emulsions. In addition to being useful in non-sensitized emulsions they may also be used in orthocromatic, panchromatic and X- ray emulsions. If used with sensitizing dyes, they may be added to the emulsion before or after the dyes are ene oxide containing from 2 to 4 carbon atoms and said alkylene oxide polymer having a molecular weight of at least 300, said emulsion containing parabanic acid as a fog inhibiting agent.
  • a light-sensitive sulfur-sensitized silver halide emulsion additionally sensitized with an alkylene oxide polymer selected from the class consisting of (l) polyalkylene glycols, (2) condensation products of alkylene oxide with glycols, (3) condensation products of alkylene oxide with aliphatic compounds selected from the class consistingot alcohols, acids and amines, (4) condensation products of alkylene oxide with phenols, and (5) condensation products of alkylene oxide with hexitol ring dehydration products, said alkylene oxide containing from 2 to 4 carbon atoms and said alkylene oxide polymer having a molecular weight of at least 300, said emulsion containing parabanic acid as a fog inhibiting agent.
  • an alkylene oxide polymer selected from the class consisting of (l) polyalkylene glycols, (2) condensation products of alkylene oxide with glycols, (3) condensation products of alkylene oxide with aliphatic compounds selected from the class consistingot alcohols, acids and amine
  • a light-sensitive sulfur-sensitized silver halide emulsion additionally sensitized with an ethylene oxide polymer having a molecular weight of at least 300, said emulsion containing parabanic acid as a fog inhibiting agent.
  • a light-sensitive sulfur-sensitized silver halide emulsion additionally sensitized with a condensation product of one mole of oleyl alcohol with approximately 15 moles of ethylene oxide, said emulsion containing parabanic acid as a fog inhibiting agent.
  • the emulsion of claim 10 which is additionally chemically sensitized with gold salts.

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Description

2,708,16l Patented May 10, 1955 PARABANIC ACID STABILIZER FOR PHOTO- GRAPHIC EMULSIONS SENSITIZED WITH ALKYLENE OXIDE POLYMERS Jean E. Jones, Rochester, N. Y., assignor to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey No Drawing. Application April 29, 1954,
Serial No. 426,542
13 Claims. (Cl. 95-7) This invention relates to fog inhibiting agents and stabilizers for photographic emulsions and to photographic emulsions containing them.
It is well known that photographic emulsions on storage tend to lose sensitivity and to become spontaneously developable Without exposure to light. There is normally a detectable amount of the silver salt reduced during development in the areas where no exposure was given; thisis commonly called fog, and sometimes called chemical fog where it is necessary to distinguish between it and the effects of accidental exposure to radiation; in this invention, I am not concerned with the latter.
. Fog depends both on the emulsionand the conditions of development; for a given emulsion it increases with the degree of development. With constant development conditions, it tends to increase with time, temperature and relative humidity of storage conditions; it is common practice to make accelerated tests of the stability of photographic emulsions by storage at increased temperature or humidity, or both. It is, of course, desirable to have emulsions as stable as possible under the conditions of high temperature and humidity which may occur in tropical climates, for example. Fog usually appears over the whole area of the sensitive coating, but when severe, it frequently is non-uniform. Fog may also be caused by exposure to chemicals, for example, hydrogen sulfide and other reactive sulfur compounds, hydrogen peroxide vapor, and strongly reducing materials. While antifoggants and stabilizers may protect, to some extent, against such effects, it is normally understood that an antifoggant protects against spontaneous growth of fog during prolonged storage or storage at high temperatures and humidities, or during development to maximum contrast and speed, or both.
It is known that the efiective sensitivityof photographic silver halide emulsions may be increased by adding to them derivatives of alkylene oxides such as ethylene oxide polymers having molecular weights of 300 or more. .The practical value of these compounds is severely limited by their tendency to increase fog on storage of the photographic film, especially storage at elevated temperatures and humidities. It has been found diflicult to control this by the antifoggants commonly available without using quantities of antifoggant which partly neutralize the speed increase obtained from the alkylene oxide derivatives.
It is therefore an object of the present invention to provide a method for stabilizing photographic emulsions sensitized with alkylene oxide derivatives such as polyethylene oxides. A further object isto provide a means for reducing the fog produced upon keeping of emulsions so sensitized, especially emulsions stored under tropical I or other adverse conditions. 'A still further object isjtoj provide a means for stabilizing the speed and contrast of emulsions so sensitized. 'Other objects will appear from the following description of my invention.
to the emulsion sensitized with alkylene oxide polymers, parabanic acid as a stabilizing and fog inhibiting agent. Parabanic acid, also known as oxalylurea and imidazoletrione, has the structure 0 0 r m-( O The alkylene oxide polymers used to sensitize the emulsions may be of various types. The alkylene oxides from which the polymers are derived contain from 2 to 4 carbon atoms, e. g., ethylene oxide, propylene oxide, and
butylene oxide. The preparation of polymers from these compounds is described in Ellis, The Chemistry of Synthetic Resins (1935), pages 990 to 994. These compounds are also referred to as polyalkylene glycols and their use as sensitizers for silver halide emulsions is described in U. S. Patents 2,423,549 and 2,441,389.
Various derivatives of alkylene oxides may also be used to sensitize the silver halide emulsions, e. g., condensation products of alkylene oxide with glycols, such as those having from 8 to 18 carbon atoms as described in U. S. Patent 2,240,472 and British Patent 443,559, as well as condensation products of alkylene oxides with aliphatic alcohols, aliphatic acids and aliphatic amines, that is, polyalkylene ethers, esters and amides, the preparation of which is described in U. S. Patent 1,970,578, condensation products of alkylene oxides with phenols, also described in U. S. Patent 1,970,578, and condensation products of alkylene oxides with hexitol ring dehydration products, as described in U. S. Patent 2,400,532.
In each case the polyalkylene oxide or derivative of alkylene oxide should have a molecular weight of at least 300. Condensation products of ethylene oxide with long chain alcohols should have a molecular weight of about 700; other derivatives may have a molecular weight of 1500 to 4000 or more.
The principal purpose of my invention is to provide means for maintaining the sensitivity and fog of silver halide emulsions at or close to initial optimum values under conditions of high temperature or high humidity, or both. Preferably, the fog inhibitor which I propose to use is added to the emulsion at any stage during the process of manufacture prior to coating the emulsion. The parabanic acid fog inhibitor may be added to the emulsion in solution in any convenient solvent not injurious to the emulsion such as lower alcohols.
Parabanic acid added at the levels needed for good antifoggant action lowers the pH of the emulsion to a considerable extent (approximately 4.8). Neutralization of the acid before addition to the emulsion, or of the emulsion after addition, diminishes the antifoggant efiect somewhat, but does not eliminate it completely. I
An additional purpose of my invention is to provide an antifoggant which may be used with emulsions sensitized with alkylene oxide polymers and which does not interfere with the action of certain gelatin hardening agents. Parabanic acid does not alfect the hardening actionof mu'cochloric acid, a-hydroxyadipaldehyde or 1,5-bis- (methane sulfonoxy)-pentane (Allen and Laakso U. S- application Serial No. 259,511, filed December 1, 1951). It does interfere somewhat with the hardening action of formaldehyde and glyoxal, although it does not prevent complete hardening in the case of formaldehyde. There appears to be little difference whether the pH of the solution of the parabanic acid which I employ when added in suitable concentration before coating to un- These objects are accomplished 'in general by adding 'sensitized or optically sensitized silver halide emulsions usually does not appreciably affect the sensitivity and fog when measurements are made soon after coating. How- Dipolyethylene glycoxy -decane H OCHzCHzO (CHaCHeO 11CH2CH2O Cir-Ha:
Polyethylene oxide oleyl other where n;an integer greater than about 10.
The preparation of silver halide emulsions involves three separate operations: (1) the emulsification and digestion or ripening of the silver halide, (2) the freeing of the emulsion from aqueous soluble salts usually by washing, (3) the second digestion or after-ripening to obtain increased sensitivity (Mees, The Theory of the Photographic Process, 1942, page 3). The fog inhibiting agents may be added at any stage, preferably after the final digestion.
The photographic emulsions which I use are of the developing-out type and .best results have been obtained with gelatino-silver bromoiodide emulsions. However, emulsions of varying halide content may .be used.
The emulsions may be chemically sensitized by any of the accepted procedures, in addition to or in combination with the sensitizing with alkylene oxide polymers. The emulsions may be digested with naturally active gelatin, or sulfur compounds may be added such as those described in Sheppard U. S. Patent 1,574,944 and 1,623,499, and Sheppard and Brigham U. S. Patent 2,410,689.
The emulsions may also be treated with salts .of the noble metals such as ruthenium, rhodium, palladium, iridium and platinum, all of which belong to group VIII of the periodic table of elements and have an atomic weight greater than 100. Representative compounds are ammonium chloropalladate, potassium chloroplatinate and sodium chloropalladite, which are used for sensitizing in amounts below that which produces any substantial fog inhibition, as described in Smith and Trivelli U. S. Patent 2,448,060, and as antifoggants in higher amounts, as described in Trivelli and Smith U. S. Patents 2,566,245 and 2,5 66,263.
The emulsions may also be chemically sensitized with gold salts as described in Waller and Dodd U. S. Patent 2,399,083, or stabilized with gold salts as described in Damschrodcr U. S. Patent 2,597,856 and Yutzy and Leermakers U. S. Patent 2,597,915. Suitable compounds are potassium chloroaurite, potassium aurithiocyanate, potassium chloroaurate, auric trichloride and 2-aurosulfobenzothiazole methochloride.
The emulsions may also be chemically sensitized with reducing agents such as stannous salts (Carroll U. S. Patent 2,487,850), polyamines such as diethylene triamine (Lowe and Jones U. S. Patent 2,518,698), polyamines 4 such as spermine (Lowe and Allen U. S. Patent 2,521,925), or bis-(fl-aminoethyl) sulfide and its watersoluble salts (Lowe and Jones U. S. Patent 2,521,926).
The emulsions may also be stabilized with the mercury compounds of Allen, Byers and Murray U. S. application Serial No. 319,611, Carroll and Murray U. S. application Serial No. 319,612 and Leubner and Murray U. S. application Serial No. 319,613, all filed November 8, 1952.
The sensitizing and stabilizing combinations of polyalkylene oxides and parabanic acid are effective in the presence or absence of optical sensitizing dyes. Since optical sensitizing may affect stability of emulsions with respect to sensitivity, fog and latent image changes, the action of parabanic acid is not completely independent of optical sensitizing or other emulsion variables. I have found, however, that both unsensitized emulsions and emulsions sensitized with cyanine or merocyanine dyes or both, may be treated with polyalkylene oxides and parabanic acid according to my invention.
The most useful concentration of parabanic acid in the emulsion is from 1 to 8 or more grams per gram mole of silver halide in the emulsion. These amounts may be used in combination with one or more of the chemical sensitizing and stabilizing agents listed above.
The stabilizing action was determined by incubation of the emulsions for a period from 1 to 4 weeks at 100 to 120 F. and constant humidity. Speeds were measured in terms of 30/E where E is the exposure required to produce a density of 0.2 above fog. The results of aging tests are tabulated in the examples below and compare speed, gamma and fog of the emulsions with and without the stabilizing compound.
Example I A negative-speed gelatino-silver bromoiodide emulsion was digested with a sulfur compound such as disclosed in Sheppard U. S. Patent 1,574,944 and potassium chloroaurate, and chemically sensitized with about 0.75 gram per gram mole of silver halide, of polyethylene oxide oleyl ether. The emulsion was then panchromatically sensitized. To portions of the emulsion there were added varying amounts of parabanic acid as shown in the following tables. Portions of the emulsions with and without the parabanic acid were coated on cellulose acetate film support, dried, exposed on an Eastman Ib Sensitometer and developed for 5 minutes at 68 F. in a developer of the following formula:
Grams N-methyl-p-aminophenol sulfate 2.5 Hydroquinone 2.5 Sodium sulfite (desiccated) 30 Sodium metaborate 10 Potassium bromide 0.5
Water to 1 liter.
Portions of the film with and without the parabanic acid were held for one week at 120 F. and constant humidity and were then exposed and developed as indicated. The results of tests for speed, gamma and fog, before and after incubation of each of the samples, were as follows:
Compound After Incubation Control. Parabanie acid {Parabanie acid solution was neutralized to pH 6.0 with 0.1 N
to emulsion.
aOH before adding Example 2 Grams N-methyl-p-aminophenol sulfate 1.5 Hydroquinone 1.3 Sodium sulfite (desiccated) 75 Borax 4.5 Potassium bromide 0.4
Water to 1 liter.
Portions of the films with and without the addenda were incubated as in Example 1, and were then exposed and developed as in the case of the fresh samples. The results were as follows:
added. Various silver salts may be used as the sensitive salt, such as silver bromide, silver iodide, silver chloride" or mixed silver halides. The parabanic acid and alkylene oxide polymers may be used in emulsions intended .for color photography, for example, emulsions containing color-forming couplers, or emulsions to be developed by solutions containing couplers.
The dispersing agents may be gelatin or other colloid such as collodion, albumen, cellulose derivatives or synthetic resins.
It will be understood that I contemplate as included within my invention all modifications and equivalents falling within the scope of the appended claims;
I claim: l. A light-sensitive silver halide emulsion sensitized with an alkylene oxide polymer selected from the class.
consisting of (1) polyalkylene glycols, (2) condensation products of alkylene oxide with glycols, (3) condensationproducts of alkylene oxide with aliphatic compounds. selected from the class consisting of alcohols, acids and amines, (4) condensation products of alkylene oxide with phenols, and (5) condensation products of alkylene oxide with hexitol ring dehydration products, said alkyl- Amount Fresh Test After Incubation Compound per mole,
Speed Gamma Fog Speed Gamma Fog Control 2, 700 68 l, 770 58 l4 Polyethylene oxide IBIIII'IO ester (I) 4, 350 68 10 2, 500 55 19 manna-5am: 8:1 4,750 44 3,000 Polyethylene oxide 01%71 ether (II) 3, 950 7O ll 2, 950 60 1o Masai-i535 3.1 4, 250 .68 10 3, 100 .66 12 Poltylethylene loxide e er g ucose mgfiolaurate (III)- g 3, 500 68 09 2, 250 56 l4 fi fi 3, 350 67 l0 2, 200 63 12 Prilyethylenied oxige auric no am e (1% 3, 800 70 10 1, 690 57 g g 3,800 .74 .10 2, 300 .62 .20 Polyethylene oxide phenyl ether (V) 8 3, 800 67 l0 2, 250 65 17 Ptiifih'iidI I: 8:1 74 14 The polyethylene oxide oleyl ether used in Example 1 was a condensation product of 1 mole of oleyl alcohol with approximately 25 moles of ethylene oxide. A similar compound (II) used in Example 2 was a condensation product of 1 mole of oleyl alcohol with approximately 15 moles of ethylene oxide.
The polyethylene oxide lauric ester (I) of Example 2 was made by condensing 1 mole of lauric acid with approximately 26 moles of ethylene oxide.
The polyethylene oxide ether of glucose monolaurate (III), the polyethylene oxide laurylamide compound (IV) and the polyethylene oxide phenyl ether (V) were prepared as described in Carroll U. S. application Serial No. 426,543, filed concurrently herewith.
The polyethylene oxide polymers used in the emulsions according to my invention may be prepared either by polymerizing ethylene oxide in the presence of aliphatic acids, aliphatic amines or phenols, or by reacting the polymerized polyethylene oxide with aliphatic acids, acid chlorides, or esters, which produces similar products.
Instead of incorporation in the silver halide emulsion, the fog inhibitor of my invention may be incorporated in a colloid layer such as a gelatin overcoating layer or interlayer in contact with the emulsion.
The fog-inhibiting agents which I have described may be used in various kinds of photographic emulsions. In addition to being useful in non-sensitized emulsions they may also be used in orthocromatic, panchromatic and X- ray emulsions. If used with sensitizing dyes, they may be added to the emulsion before or after the dyes are ene oxide containing from 2 to 4 carbon atoms and said alkylene oxide polymer having a molecular weight of at least 300, said emulsion containing parabanic acid as a fog inhibiting agent.
2. A light-sensitive silver halide emulsion sensitized with an ethylene oxide polymer having a molecular weight of at least 300, said emulsion containing parabanic acid as a fog inhibiting agent.
3. A light-sensitive silver halide emulsion sensitized with a condensation product of ethylene oxide with an aliphatic alcohol, said condensation product having a molecular Weight of at least 300, and said emulsion containing parabanic acid as a fog inhibiting agent.
4. A light-sensitive silver halide emulsion sensitized with a condensation product of ethylene oxide with an aliphatic acid, said condensation product having a molecular weight of at least 300, and said emulsion containing parabanic acid as a fog inhibiting agent.
5. A light-sensitive silver halide emulsion sensitized with a condensation product of ethylene oxide with a phenol, said condensation product having a molecular weight of at least 300, and said emulsion containing parabanic acid as a fog inhibiting agent.
6. A light-sensitive silver halide emulsion sensitized with a condensation product of ethylene oxide with glucose monolaurate, said condensation product having a molecular weight of at least 300, and said emulsion containing parabanic acid as a fog inhibiting agent.
7. A light-sensitive silver halide emulsion sensitized with a condensation product of ethylene oxide with lauric acid amide, said condensation product having a molecular weight of at least 300, and said emulsion containing paraba'nic acid as a fog inhibiting agent.
8. A light-sensitive silver halide emulsion sensitized with a condensation product of one mole of oleyl alcohol with approximately 15 moles of ethylene oxide, said emulsion containing parabanic acid as a fog inhibiting agent.
9. A light-sensitive sulfur-sensitized silver halide emulsion additionally sensitized with an alkylene oxide polymer selected from the class consisting of (l) polyalkylene glycols, (2) condensation products of alkylene oxide with glycols, (3) condensation products of alkylene oxide with aliphatic compounds selected from the class consistingot alcohols, acids and amines, (4) condensation products of alkylene oxide with phenols, and (5) condensation products of alkylene oxide with hexitol ring dehydration products, said alkylene oxide containing from 2 to 4 carbon atoms and said alkylene oxide polymer having a molecular weight of at least 300, said emulsion containing parabanic acid as a fog inhibiting agent.
10. A light-sensitive sulfur-sensitized silver halide emulsion additionally sensitized with an ethylene oxide polymer having a molecular weight of at least 300, said emulsion containing parabanic acid as a fog inhibiting agent.
11. A light-sensitive sulfur-sensitized silver halide emulsion additionally sensitized with a condensation product of one mole of oleyl alcohol with approximately 15 moles of ethylene oxide, said emulsion containing parabanic acid as a fog inhibiting agent.
12. The emulsion of claim 9 which is additionally chemically sensitized withgold salts.
13. The emulsion of claim 10 which is additionally chemically sensitized with gold salts.
No references cited.

Claims (1)

1. A LIGHT-SENSITIVE SILVER HALIDE EMULSION SENSITIZED WITH AN ALKYLENE OXIDE POLYMER SELECTED FROM THE CLASS CONSISTING OF (1) POLYALKYLENE GLYCOLS, (2) CONDENSATION PRODUCTS OF ALKYLENE OXIDE WITH GLYCOLS, (3) CONDENSATION PRODUCTS OF ALKYLENE OXIDE WITH ALIPHATIC COMPOUNDS SELECTED FROM THE CLASS CONSISTING OF ALCOHOLS, ACIDS AND AMINES, (4) CONDENSATION PRODUCTS OF ALKYLENE OXIDE WITH PHENOLS, AND (5) CONDENSATION PRODUCTS OF ALKLYLENE OXIDE WITH HEXITOL RING DEHYDRATION PRODUCTS, SAID ALKYLENE OXIDE CONTAINING FROM 2 TO 4 CARBON ATOMS AND SAID ALKYLENE OXIDE POLYMER HAVING A MOLECULAR WEIGHT OF AT LEAST 300, SAID EMULSION CONTAINING PARABANIC ACID AS A FOG INHIBITING AGENT.
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2948614A (en) * 1957-07-11 1960-08-09 Stabilized photographic silver halede
DE1095114B (en) * 1957-05-01 1960-12-15 Du Pont Stabilized water-permeable photographic silver halide layer
DE1096194B (en) * 1957-05-01 1960-12-29 Du Pont Stabilized photographic silver halide layer
DE1108074B (en) * 1958-04-14 1961-05-31 Gen Aniline & Film Corp Light sensitive photographic silver halide layers and material containing them
DE1188438B (en) * 1961-03-13 1965-03-04 Du Pont Photographic silver halide emulsion to be used for lithographic films, plates or the like
US3287135A (en) * 1963-12-20 1966-11-22 Eastman Kodak Co Antifoggants for silver halide emulsions on a linear polyester support
US4411987A (en) * 1981-11-06 1983-10-25 Fuji Photo Film Co., Ltd. Silver halide color photographic light-sensitive material
US4419443A (en) * 1980-11-11 1983-12-06 Fuji Photo Film Co., Ltd. Silver halide photographic light-sensitive material

Non-Patent Citations (1)

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

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1095114B (en) * 1957-05-01 1960-12-15 Du Pont Stabilized water-permeable photographic silver halide layer
DE1096194B (en) * 1957-05-01 1960-12-29 Du Pont Stabilized photographic silver halide layer
US2948614A (en) * 1957-07-11 1960-08-09 Stabilized photographic silver halede
DE1108074B (en) * 1958-04-14 1961-05-31 Gen Aniline & Film Corp Light sensitive photographic silver halide layers and material containing them
DE1188438B (en) * 1961-03-13 1965-03-04 Du Pont Photographic silver halide emulsion to be used for lithographic films, plates or the like
DE1284289B (en) * 1961-03-13 1968-11-28 Du Pont Process for the preparation of a gelatin-containing silver halide photographic emulsion for lithographic use
US3287135A (en) * 1963-12-20 1966-11-22 Eastman Kodak Co Antifoggants for silver halide emulsions on a linear polyester support
US4419443A (en) * 1980-11-11 1983-12-06 Fuji Photo Film Co., Ltd. Silver halide photographic light-sensitive material
US4411987A (en) * 1981-11-06 1983-10-25 Fuji Photo Film Co., Ltd. Silver halide color photographic light-sensitive material

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