US2276323A - Photographic silver halide emulsion - Google Patents

Photographic silver halide emulsion Download PDF

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US2276323A
US2276323A US368661A US36866140A US2276323A US 2276323 A US2276323 A US 2276323A US 368661 A US368661 A US 368661A US 36866140 A US36866140 A US 36866140A US 2276323 A US2276323 A US 2276323A
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silver halide
emulsion
polyvinyl
vinyl
acetate
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Wesley G Lowe
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Eastman Kodak Co
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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
    • G03C1/04Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
    • G03C1/053Polymers obtained by reactions involving only carbon-to-carbon unsaturated bonds, e.g. vinyl polymers

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  • This invention relates to a method of making photographic silver halide emulsions in which the silver halide is first prepared in an aqueous solution of a silver halide dispersing agent and the dispersion is subsequently thoroughly mixed with a hydrolyzed polyvinyl acetate of 59-7l%, or a hydrolyzed polyvinyl acylate of 0.5-5% vinyl acylate content and the.
  • emulsion these previously proposed materials often evidence inferiority in one or more of the proper-ties enumeratedabove with respect to gelatin. For example, cellulose nitrate has been suggested for use in this connection.
  • Another object of my inven' tion is to provide a method of making photographic silver halide emulsions in which the silver halide is efiectively dispersed therein.
  • a further object of my invention is to prepare photographic silver halide emulsions from which pictures may be obtained comparable to those obtained with other photographic emulsions of good quality. Other objects of my invention will appear herein.
  • Gelatintas a protective colloid in photographic silver halide emulsions does have disadvantages. It is vulnerable to attack by animal and vegetable life. For instance, insects attack gelatin, particularly inthe'tropics. 'Also it is susceptible to the action of mold and of bacteria, particularly under processes readily in the conventional developing and fixing baths. I have found that by preparing a photographic emulsion in this manner the silver halide is carried in the emulsion in a finely divided form, that the emulsion is easily coated onto' a support and that it can readily be set and dried to a hard scratch-resistant emulsion layer which may be treated with developing and fixing baths (as is usual after exposing) and washed thoroughly with water without dissolving. Even though the polyvinyl acetate of 0.5- I
  • 5% vinyl acetate content is water soluble, it does not dissolve 01? due perhaps partly to the action of the salts present inthe processing baths.
  • the resulting emulsion layer exhibits good physical properties. If a washed emulsion is desired with a polyvinyl acetate of 0.5-5% yinyl acetate-content, it is desirable to treat the emulsion after its formation with a gelling agent as described and claimed in McDowell and Kenyon applications Nos. 318,550; 318,551; 318,552 and 318,553, filed February 12, 1940. Treatment of the emulsions .with a gelling agent such as betanaphthyl salihigh humidity conditions.
  • Gelatin is a product of nature and is obtained from a wide variety and assortment of materials from widely scattered points," both geographical and physiological.
  • One object of my invention is to provide a method of making photographic silver, halide emulsions of good quality in which a highly reacetate is present in a concentration of approximately 13-10%, a gelling agent is addedthereto at an elevated temperature (preferably 40-90 C.)
  • the emulsion may then be washed with water sufficiently to remove the water soluble salts resulting from the formation of the silver halide if desired, without detrimentally affecting the polyvinyl .material.
  • the gel, washed or unwashed can be warmed to cause the formation of a sol and can be applied in the form or a thin layer to a support for the emulsion.
  • the emulsion layer can then be set by cooling, followed by drying in the usual manner.
  • the preparation of silver halide for the emulsion iscarried out in a very dilute aqueous solution of a material which has the power of preventing the agglomeration of th particles of silver halide when they form. It must also becompatible with the polyvinyl acetate used as the a protective colloid. Any material having these properties may be employed, these materials beacetate prepared from awater-soluble starch was hydrolyzed to prepare it. It is desirablethat the starch acetate employed be of a1ow viscosity type. k
  • Another suitable silver halide dispersing agent is the co-polymer of maleic anhydride and vinyl acetate having an apparent molecular weight of the order of magnitude 30,000-200,000 (based on viscosity measurements) as described in U. S. Patent No. 2,047,398 of I G.
  • the condensation product of this co-polymer of maleic anhydride and vinyl-acetate with aniline as described in the U. S. patent to I. G. referred to, has also been found to be useful for dispersing silver halide in accordance with the process of my invention.
  • Water soluble lower alkyl cellulose ethers have also been found to be suitable for dispersing silver halides in my process.
  • water soluble methyl cellul-oses having a methoxy content of 20-30% are particularly suitable for this purpose.
  • Other lower alkyl celluloses having corresponding alkoxy contents are suitable for this purpose.
  • Other materials having the properties. prescribed for a silver halide dispersing agent are suitable for use herein for that purpose. For, instance: both gum arabic as commercially available and water-soluble urea-formaldehyde condensation products have been found quite.
  • the silver halide dispersing agents are employed in preparing silver halide in the form of dilute aqueous solutions. For instance, a, dilution of the dispersing agent in an aqueous liquid in a concentration within the range 'of 0.5-6% of dispersing agent is ordinarily employed. It is to,be understood, however,'that the proportion of silver halide dispersing agent may vary in accordance with the ju gment of the individual operator. For example if greater contrast is de- 6 should be within the range of approximately.
  • the ratio to .35 content of 0.5-5% or of 59-71% is thenadded daolyvinyl acetate of: approximately 1:5 may be g as ethyl alcohol will aid the dispersing power so that a lower ratio, such as 1:10, will give good results.
  • the mixing of a little silver halide.
  • the moderately high viscosity esters such as 'of cps. have been found quite satisfactory for this purpose.
  • the polyvinyl acetates of 59-71% acetyl and-the propionates and butyrates having corresponding properties which are useful may also be of low, medium, or high viscosity and may have viscosities corresponding to those of the low acetyl polyvinyl acetates.
  • the useful polyvinyl acetates are derived from fully esterified polyvinyl acetates by hydrolysis and the viscosity of the polyvinyl acetate in its hydrolyzed form is governed by'the viscosity of vinyl acetate.
  • the photographic silver halide emulsions of my invention may be prepared by a process involving first the preparation of a dispersion of silver halide accomplished by running aqueous solutions of silver nitrate and alkali metal halide into anagitated dilute aqueous solution of a the original polysilyer halide dispersing agent.- An aqueous solu-' tion of a polyvinyl acetate having a vinyl acetate and thoroughly incorporated in the mass such as by stirring the materials together for a few minutes.
  • polyvinyl acetates of 59-71% vinyl acetate content are not water-soluble, a small amount of a water-miscible solvent such 'as acetone, ethyl alcohol, dioxane, methyl or ethyl cellosolve which when mixed with water will 50- complish the dissolution of the polyvinyl acetate solution of the polyvinyl acetate of high. acetyl content)
  • The. mass which maybe termed an emulsion may, with or without warming followed by cooling, be sensitized with a small amount of to form a hard, scratch-resistant, light-sensitive emulsion layer. 7 It may then .be exposed, processed, washed and dried and good prints will result.
  • aqueous developing and fixing baths usually.employed with gelatin emulsions are'usutain a faster emulsion a larger proportion of sensitizing dye should be incorporated;
  • a fast emulsion is useful in the direct p hdtographing of obused'although the addition or-some solvent such 75, and where developing is not to'be employed.
  • cellulose ester support usual types are cellulose nitrate sheeting, cellulose acetate sheeting,
  • Photographic silver halide emulsions maybe sensitized in this same manner as are silver halide emulsions generally.
  • Sensitizers which have been previously employed to optically sensitize silver halide emulsions may be incorporated in the emulsions described herein to-increase their sensitiivty. These emulsions are susceptible to sensitization by cyanine sensitizing dyes or by the sensitizing dyes which are described in the following patents: U. S. No. 2,078,233 of Brooker, dated April 27, 1937; U. S. No. 2,166,736 of White et al., dated July 18, 1939; U. S. No.
  • the sensitized emulsions prepared in accordance with my invention are particularly valuable in recording the image of an object.
  • the emulsions of my invention may be toned blue or they may be used in color processes and colored with dyes which resist diffusion.
  • the following examples illustrate my invention:
  • Example 1 Ten grams of a cellulose ethyl ether known as :Hyglin containing approximately 25-28% ethoxy, was dissolved in 190 cc. of water. Twenty grams of 'this solution was taken, was diluted with 40 cc. of water, heated to 80 F. and rapidly stirred while solutions A and B were run in simultaneously over an interval of three minutes. Solutions A and B were identical to those listed in the preceding example under these designations. Fifty grams of a 10% aqueous solution of high viscosity polyvinyl acetate having a vinyl acetate content of less than 5% and 25 cc. of water was added and thoroughly incorporated into the mixture. The emulsion was then sensitized by incorporating 2 mg. of 2,3'-diethyl 4' methyloxathiazolocarbocyanine iodide. The emulsion was then coated on paper and dried and upon exposing the emulsion was processed and was found to give prints of good quality.
  • Example 3 Ten grams of a low viscosity methyl cellulose having a methoxyl content of approximately 28% was dissolved in 290 cc. of water. Fifteen grams of this solution was taken, diluted with a mixture of 15 cc. of water and 15 cc. of ethyl alcohol and the resulting solution was stirred briskly and heated to 80 F. Solutions A and B (identified in Example 1) were introduced si multaneously with rapid stirring over an inter- Twenty grams of low viscosity starch acetate having an acetyl content of 11% were dissolved in 100 cc. of water. Ten grams of thissolution was taken and was diluted with 40 cc. of water.
  • Solution B A mixture of aqueous solutions of KBr, KCl, and K1 in the following amounts and concentrations:
  • Example 4 One gram of gum arabic was dissolved in 50 cc. of water at F.-and rapidly stirred while solutions A and B (identified in Example 1) were run in simultaneously over an interval of three minutes. At the end of this time 60 grams of a 10% aqueous solution of high viscosity polyvinyl acetate having a vinyl acetate content of 8 less than 5% and 25 cc. of water was added. The emulsion was sensitized by incorporating therein 2 mg. of 2,3-diethyl-4'-methyloxathiazolocarbocyanine iodide. The emulsion was coated and dried on paper and gave prints of satisfactory quality when treated in the usual manner.
  • Example 5 neously over an interval of three minutes.- At
  • Example 6 0.5 gram of the condensation product of a maleic anhydride-vinyl acetate resin and aniline was dissolved in 50 cc. of water at a temperature vof 80 F. and rapidly stirred while solutions A and B (identified in Example 1) were run in simultaneously over an interval of three minutes. At the end of this time 60 grams of a 10% aque ous solution of high viscosity polyvinyl acetate having a vinyl acetate content of less than and 25 cc. of Water was added. The emulsion was sensitized by incorporating therein 2 mg. of 2,3'- diethyl 4'-methyloxathiazolocarbocyanine iodide. The emulsion was coated and dried on paper and gave prints of satisfactory quality when treated in the usual manner.
  • a hydrolyzed polyvinyl acetate having a vinyl acetate content of 59'7l% may be employed as the vehicle in any of the preceding examples.
  • a hydrolyzed polyvinyl acetate having a vinyl acetate content of 59'7l% may be employed as the vehicle in any of the preceding examples.
  • Example 1 instead of adding 60 grams of a solution of high viscosity polyvinyl acetate of low vinyl acetate content, 60 grams of a 6% solution of polyvinyl acetate (containing 59% vinyl acetate) dissolved in a mixture of 2 parts of acetone in 3 parts of water may be employed to supply the vehicle.
  • the emulsion may be plasticized by some compatible softening or plasticizing agent, such as monoacetin.
  • polyvinyl esters prescribed as useful in my emulsions have a polyvinyl acylate content of less than 5% or have a polyvinyl acetate content within the range of 59-7l%, the remainder of the compound being polyvinyl alcohol.
  • the silver halide may be prepared and dispersed in an aqueous solution containing in addition to the silver halide dispersing agent some or all of the polyvinyl acetate.
  • the polyvinyl acetates having a vinyl acetate content of less than 5% water only may be used as the solvent.
  • the solvent In the case of polyvinyl acetates having a vinyl acetate content of 59- 71% it is. of course, necessary to also use a small amount of organic solvent with the water employed as the solvent medium.
  • the hydrolyzed water-permeable polyvinyl propionates or butyrates which are most suitable for use in preparing photographic silver halide emulsions are those having a sufficient permeability to allow development for the emulsion but suflicient insolubility to resist dissolving by the processing baths.
  • These polyvinyl propionates or butyrates may be identified by their similarity in these properties to the polyvinyl acetates having a vinyl acetate content of 59--7l%.
  • vinyl derivatives which are found to have suitable properties for use as carriers in photographic emulsions such as selected from the vinyl dicarboxylates or hydroi'iy esters hydroxy acid esters of vinyl, or the hydrolyzed copolymer of vinyl acetate with a small proporof carboxylates, the 4 tion of another polymerizable compound such as vinyl chloride, styrene, an acrylic acid ester or the like might be employed to form a photographic emulsion as described herein.
  • a method of preparing photographic silver halide emulsions which comprises preparing the silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto a protective colloid selected from the group consisting of the polyvinyl lower fatty acid esters having a vinyl acylate content of 0.5-5% and the polyvinyl acetates of 59-71% vinyl acetate content, substantially theremainder being vinyl alcohol.
  • a method of preparing photographic silver halide emulsions which comprises preparing the silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding a protective colloid thereto selected from the group consisting of the polyvinyl acetates having vinyl acetate contents of 0.55% and 59-71%, substantially the remainder being vinyl alcohol.
  • a method of preparing photographic silver halide emulsions which comprises preparing silver halide in an aqueous solution of a water soluble starch acetate and subsequently adding a protective colloid selected from the group consisting of the polyvinyl lower fatty acid esters having vinyl acylate contents of 0.55% and the polyvinyl acetates having vinyl acetate contents of 597l%, substantially the remainder being vinyl alcohol.
  • a method of preparing photographic silver halide emulsions which comprises preparing silver halide in an aqueous solution of a water soluble lower alkyl cellulose and subsequently adding a protective colloid selected from the group consisting of polyvinyl lower fatty acid esters having vinyl acylate contents of 0.55% and the polyvinyl acetates having vinyl acetate contents of 59'7l substantially the remainder being vinyl alcohol.
  • a method of preparing photographic silver halide emulsions which comprises preparing silver halide in an aqueous solution of a maleic anhydride-vinyl acetate resin and subsequently adding a protective colloid selected from the group consisting of polyvinyl lower fatty acid esters having vinyl acylate contents of 05-23% and polyvinyl acetates having vinyl acetate contents of 59-7l%, substantially the remainder being vinyl alcohol.
  • a method of preparing photographic silver halide emulsions which comprises preparing 'a silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto an optical sensitizer and a protective colloid selected from the group consisting of polyvinyl lower fatty acid esters having vinyl acylate contents of 0.5-5% and polyvinyl acetates having vinyl acetate contents of 59-7l%, substantially the remainder being vinyl alcohol.
  • a method of preparing photographic silver halide emulsions which comprises preparing a silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto a polyvinyl acetate having a vinyl acetate content of 0.5-5%, substantially the remainder being vinyl alcohol.
  • a method of preparing photographic silver halide, emulsions which comprises preparing a silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto a polyvinyl acetate having a vinyl acetate content of 59-71%, substantially the remainder being vinyl alcohol.
  • a photographic silver halide emulsion comprising a finely dispersed silver halide resulting from preparing it in an aqueous solution of a silver halide dispersing agent and a protective colloid selected. from the group consisting of polyvinyl lower fatty acid esters having vinyl acylate contents of 0.5-% and polyvinyl acetates having vinyl acetate contents of 59-71%, substantially the remainder being vinyl alcohol.
  • a photographic silver halide emulsion comprising a finely dispersed silver halide resulting comprising a finely dispersed silver halide re-' sulting from its preparation in an aqueous solution of a silver halide dispersing agent and as the protective colloid a polyvinyl acetate having a vinyl acetate content of 0.5-5%, substantially the remainder being vinyl alcohol.
  • a photographic silver halide emulsion comprising a finely dispersed silver halide resulting from its preparation in an aqueous solution of a silver halide dispersing agent and as a protective colloid a polyvinyl acetate having a vinyl acetate content of 59-71%, substantially the remainder being vinyl alcohol.
  • a photographic silver halide emulsion comprising a finely dispersed silver halide in a mixture of a silver halide dispersing agent. and a polyvinyl acetate selected from the group consisting of the polyvinyl acetates having vinyl acetate contents of 0.55% and of 59-71%, substantially the remainder being vinyl alcohol.
  • a photographic silver halide emulsion comprising a finely dispersed silver halide in a mixture of a water-soluble starch acetate and a polyvinyl fatty acid ester having a vinyl acylate content of 0.5-5%, substantially the remainder being vinyl alcohol.

Description

Patente Mar. 1?, l l
rnorocmrnic srivea z s Wesley G. Lowe, Rochester, N. Y., assignor to Eastman Kodak tlompany,- Rochester, N. Y a corporation or New Jersey No Drawing. Application December 5, 1940, Serial No. 368,661
*fin'ed synthetic material may be employed as the 14 Claims.
This application is a continuation-impart of my application Serial No, 318,560 entitled, Pho-' tographic silver halide emulsions, filed February 12, 1940.
This invention relates to a method of making photographic silver halide emulsions in which the silver halide is first prepared in an aqueous solution of a silver halide dispersing agent and the dispersion is subsequently thoroughly mixed with a hydrolyzed polyvinyl acetate of 59-7l%, or a hydrolyzed polyvinyl acylate of 0.5-5% vinyl acylate content and the. emulsion these previously proposed materials often evidence inferiority in one or more of the proper-ties enumeratedabove with respect to gelatin. For example, cellulose nitrate has been suggested for use in this connection. This material-when dry is not very permeable to the conventional aquelowed by the mixing therewith of a substantial protective colloid.- Another object of my inven' tion is to provide a method of making photographic silver halide emulsions in which the silver halide is efiectively dispersed therein. A further object of my invention is to prepare photographic silver halide emulsions from which pictures may be obtained comparable to those obtained with other photographic emulsions of good quality. Other objects of my invention will appear herein. I have found that if silver halide is prepared in an aqueous solution containing a substantial amount of a silver halide dispersing agent, folamount of a protective colloid selected from the group'consisting of the polyvinyl acetates having vinyl acetate contents of 0.5-5% and of 59-71%,
' an emulsion results which gives clean results and ous developing and fixing baths. Also cellulose nitrate is insoluble in a solvent mixture containing-an appreciable .amount of water and, there-' l fore, water-soluble salts cannot be used with cellulose nitrate'to prepare a silver halide. I
Gelatintas a protective colloid in photographic silver halide emulsions does have disadvantages. It is vulnerable to attack by animal and vegetable life. For instance, insects attack gelatin, particularly inthe'tropics. 'Also it is susceptible to the action of mold and of bacteria, particularly under processes readily in the conventional developing and fixing baths. I have found that by preparing a photographic emulsion in this manner the silver halide is carried in the emulsion in a finely divided form, that the emulsion is easily coated onto' a support and that it can readily be set and dried to a hard scratch-resistant emulsion layer which may be treated with developing and fixing baths (as is usual after exposing) and washed thoroughly with water without dissolving. Even though the polyvinyl acetate of 0.5- I
5% vinyl acetate content is water soluble, it does not dissolve 01? due perhaps partly to the action of the salts present inthe processing baths. The resulting emulsion layer exhibits good physical properties. If a washed emulsion is desired with a polyvinyl acetate of 0.5-5% yinyl acetate-content, it is desirable to treat the emulsion after its formation with a gelling agent as described and claimed in McDowell and Kenyon applications Nos. 318,550; 318,551; 318,552 and 318,553, filed February 12, 1940. Treatment of the emulsions .with a gelling agent such as betanaphthyl salihigh humidity conditions. Gelatin is a product of nature and is obtained from a wide variety and assortment of materials from widely scattered points," both geographical and physiological.
Therefore, it is subject-to considerable variation in properties from time to time. To obtain gelacylamide, gallic acid, resorcinol, or alpha ,naphthol inthe manner prescribed in those ap- .plications converts the emulsion to a rigid thermo-reversible gel. For instance, after forming the photographic em'ulsion with the low acetyl polyvinyl acetate in which emulsion the polyvinyl tin in a highly refined condition (as needed for photographic purposes) requires considerable care and it can be procuredonly in limited amounts from animal products by' a slow. and expensive P ms-- --One object of my invention is to provide a method of making photographic silver, halide emulsions of good quality in which a highly reacetate is present in a concentration of approximately 13-10%, a gelling agent is addedthereto at an elevated temperature (preferably 40-90 C.)
and the mass; is then cooled to form a rigid gel.
The emulsion may then be washed with water sufficiently to remove the water soluble salts resulting from the formation of the silver halide if desired, without detrimentally affecting the polyvinyl .material. If desired, the gel, washed or unwashed, can be warmed to cause the formation of a sol and can be applied in the form or a thin layer to a support for the emulsion. The emulsion layer can then be set by cooling, followed by drying in the usual manner.
The preparation of silver halide for the emulsion iscarried out in a very dilute aqueous solution of a material which has the power of preventing the agglomeration of th particles of silver halide when they form. It must also becompatible with the polyvinyl acetate used as the a protective colloid. Any material having these properties may be employed, these materials beacetate prepared from awater-soluble starch was hydrolyzed to prepare it. It is desirablethat the starch acetate employed be of a1ow viscosity type. k
Another suitable silver halide dispersing agent is the co-polymer of maleic anhydride and vinyl acetate having an apparent molecular weight of the order of magnitude 30,000-200,000 (based on viscosity measurements) as described in U. S. Patent No. 2,047,398 of I G. The condensation product of this co-polymer of maleic anhydride and vinyl-acetate with aniline as described in the U. S. patent to I. G. referred to, has also been found to be useful for dispersing silver halide in accordance with the process of my invention. Water soluble lower alkyl cellulose ethers have also been found to be suitable for dispersing silver halides in my process. Ordinarily the water soluble methyl cellul-oses having a methoxy content of 20-30% are particularly suitable for this purpose. Other lower alkyl celluloses having corresponding alkoxy contents are suitable for this purpose. Other materials having the properties. prescribed for a silver halide dispersing agent are suitable for use herein for that purpose. For, instance: both gum arabic as commercially available and water-soluble urea-formaldehyde condensation products have been found quite.
satisfactory'in preparing silver halide in a finely dispersed form, in accordance with my invention.
The silver halide dispersing agents are employed in preparing silver halide in the form of dilute aqueous solutions. For instance, a, dilution of the dispersing agent in an aqueous liquid in a concentration within the range 'of 0.5-6% of dispersing agent is ordinarily employed. It is to,be understood, however,'that the proportion of silver halide dispersing agent may vary in accordance with the ju gment of the individual operator. For example if greater contrast is de- 6 should be within the range of approximately.
0.5:6-4:,6 .(by weight). For example, in the'case of watcrsoluble methyl cellulose, the ratio to .35 content of 0.5-5% or of 59-71% is thenadded daolyvinyl acetate of: approximately 1:5 may be g as ethyl alcohol will aid the dispersing power so that a lower ratio, such as 1:10, will give good results. In some-cases the mixing" of a little silver halide. Any of the polyvinyl esters having a VinyLacyI-ate content of less than 5% and .a viscosity of from 2-60 cps. may be employed as protective colloids for the silver halide The moderately high viscosity esters such as 'of cps. have been found quite satisfactory for this purpose. The polyvinyl acetates of 59-71% acetyl and-the propionates and butyrates having corresponding properties which are useful may also be of low, medium, or high viscosity and may have viscosities corresponding to those of the low acetyl polyvinyl acetates. The useful polyvinyl acetates are derived from fully esterified polyvinyl acetates by hydrolysis and the viscosity of the polyvinyl acetate in its hydrolyzed form is governed by'the viscosity of vinyl acetate.
The photographic silver halide emulsions of my invention may be prepared by a process involving first the preparation of a dispersion of silver halide accomplished by running aqueous solutions of silver nitrate and alkali metal halide into anagitated dilute aqueous solution of a the original polysilyer halide dispersing agent.- An aqueous solu-' tion of a polyvinyl acetate having a vinyl acetate and thoroughly incorporated in the mass such as by stirring the materials together for a few minutes. As the polyvinyl acetates of 59-71% vinyl acetate content are not water-soluble, a small amount of a water-miscible solvent such 'as acetone, ethyl alcohol, dioxane, methyl or ethyl cellosolve which when mixed with water will 50- complish the dissolution of the polyvinyl acetate solution of the polyvinyl acetate of high. acetyl content) The. mass which maybe termed an emulsion may, with or without warming followed by cooling, be sensitized with a small amount of to form a hard, scratch-resistant, light-sensitive emulsion layer. 7 It may then .be exposed, processed, washed and dried and good prints will result. The aqueous developing and fixing baths usually.employed with gelatin emulsions are'usutain a faster emulsion a larger proportion of sensitizing dye should be incorporated; A fast emulsion is useful in the direct p hdtographing of obused'although the addition or-some solvent such 75, and where developing is not to'be employed. I
must be used with water in forming the aqueous cellulose ester or a synthetic resin support. The
usual types of cellulose ester support are cellulose nitrate sheeting, cellulose acetate sheeting,
or sheeting prepared from mixed esters of cellulose Ordinarily it is unnecessary to wash the emulsion when coating upon a paper support is contemplated. If a cellulose ester support is to be used, the coating thereon of a washed emulsion which has been sensitized gives a good quality photographic film.
Photographic silver halide emulsions maybe sensitized in this same manner as are silver halide emulsions generally. Sensitizers which have been previously employed to optically sensitize silver halide emulsions may be incorporated in the emulsions described herein to-increase their sensitiivty. These emulsions are susceptible to sensitization by cyanine sensitizing dyes or by the sensitizing dyes which are described in the following patents: U. S. No. 2,078,233 of Brooker, dated April 27, 1937; U. S. No. 2,166,736 of White et al., dated July 18, 1939; U. S. No. 2,186,608 of Keyes, dated January 9, 1940; and U. S. No. 2,165,339 of Brooker, dated July 11, 1939, depending upon, the type and range of sensitivity desired. The sensitized emulsions prepared in accordance with my invention are particularly valuable in recording the image of an object. The emulsions of my invention may be toned blue or they may be used in color processes and colored with dyes which resist diffusion. The following examples illustrate my invention:
Example 1 Example 2 Ten grams of a cellulose ethyl ether known as :Hyglin containing approximately 25-28% ethoxy, was dissolved in 190 cc. of water. Twenty grams of 'this solution was taken, was diluted with 40 cc. of water, heated to 80 F. and rapidly stirred while solutions A and B were run in simultaneously over an interval of three minutes. Solutions A and B were identical to those listed in the preceding example under these designations. Fifty grams of a 10% aqueous solution of high viscosity polyvinyl acetate having a vinyl acetate content of less than 5% and 25 cc. of water was added and thoroughly incorporated into the mixture. The emulsion was then sensitized by incorporating 2 mg. of 2,3'-diethyl 4' methyloxathiazolocarbocyanine iodide. The emulsion was then coated on paper and dried and upon exposing the emulsion was processed and was found to give prints of good quality.
Example 3 Ten grams of a low viscosity methyl cellulose having a methoxyl content of approximately 28% was dissolved in 290 cc. of water. Fifteen grams of this solution was taken, diluted with a mixture of 15 cc. of water and 15 cc. of ethyl alcohol and the resulting solution was stirred briskly and heated to 80 F. Solutions A and B (identified in Example 1) were introduced si multaneously with rapid stirring over an inter- Twenty grams of low viscosity starch acetate having an acetyl content of 11% were dissolved in 100 cc. of water. Ten grams of thissolution was taken and was diluted with 40 cc. of water.
This diluted starch acetate was rapidly stirred together with solutions A and B at a temperature of 80 F. Solutions A and B are as follows:
Solution A.-10 cc. of aqueous silver nitrate solution at 80 F.
Solution B.-A mixture of aqueous solutions of KBr, KCl, and K1 in the following amounts and concentrations:
cc. 40% KB! 8.5 25% KCl 0.5 25% KI 0.5
.and the photographic quality was good. The
prints prepared from this solution ferrotyped easily to a high gloss. It is to be understood that in this all the succeeding examples, the preparation of the emulsion beginning with preparing the silver halide was carried out in the absence of sufiicient light to detrimentally affect the light-sensitive properties of the emulsion.
val of three minutes. -50 grams of a 10% aqueous solution of high viscosity polyvinyl acetate having a vinyl acetate content of less than 5% and 20 cc. of water was added. The emulsion was sensitized by adding 2 mg. of 2,3'-diethyl-4'- methyloxathiazolocarbocyanine iodide, and thoroughly stirring the mass. This emulsion was found to .coat and dry well on paper and gave good prints upon exposure and processing in the usual manner. l
Example 4 One gram of gum arabic was dissolved in 50 cc. of water at F.-and rapidly stirred while solutions A and B (identified in Example 1) were run in simultaneously over an interval of three minutes. At the end of this time 60 grams of a 10% aqueous solution of high viscosity polyvinyl acetate having a vinyl acetate content of 8 less than 5% and 25 cc. of water was added. The emulsion was sensitized by incorporating therein 2 mg. of 2,3-diethyl-4'-methyloxathiazolocarbocyanine iodide. The emulsion was coated and dried on paper and gave prints of satisfactory quality when treated in the usual manner.
Example 5 neously over an interval of three minutes.- At
the end of this time 60 grams of a 10% aqueous solution of high viscosity polyvinyl acetate having a vinyl acetate content ofless than 5% and 25 cc. of water was added. The emulsion was sensitized by incorporating therein 2 mg. of 2,3- diethyl 4 methyloxathiazolocarbocyanine iodide. The emulsion was coated and dried on paper and gave prints of satisfactory qualitywhen treated in the usual manner.
Example 6 0.5 gram of the condensation product of a maleic anhydride-vinyl acetate resin and aniline was dissolved in 50 cc. of water at a temperature vof 80 F. and rapidly stirred while solutions A and B (identified in Example 1) were run in simultaneously over an interval of three minutes. At the end of this time 60 grams of a 10% aque ous solution of high viscosity polyvinyl acetate having a vinyl acetate content of less than and 25 cc. of Water was added. The emulsion was sensitized by incorporating therein 2 mg. of 2,3'- diethyl 4'-methyloxathiazolocarbocyanine iodide. The emulsion was coated and dried on paper and gave prints of satisfactory quality when treated in the usual manner.
Instead of using a polyvinyl acetate having a low vinyl acetate content, a hydrolyzed polyvinyl acetate having a vinyl acetate content of 59'7l% may be employed as the vehicle in any of the preceding examples. For instance, in Example 1, instead of adding 60 grams of a solution of high viscosity polyvinyl acetate of low vinyl acetate content, 60 grams of a 6% solution of polyvinyl acetate (containing 59% vinyl acetate) dissolved in a mixture of 2 parts of acetone in 3 parts of water may be employed to supply the vehicle. Instead of a polyvinyl acetate of 59% vinyl acetate, one having 71% by weight of vinyl acetate or one having a vinyl acetate content within the range of 59-'71% may be employed. If desired, the emulsion may be plasticized by some compatible softening or plasticizing agent, such as monoacetin.
It is to be understood that the polyvinyl esters prescribed as useful in my emulsions have a polyvinyl acylate content of less than 5% or have a polyvinyl acetate content within the range of 59-7l%, the remainder of the compound being polyvinyl alcohol.
As an alternative procedure the silver halide may be prepared and dispersed in an aqueous solution containing in addition to the silver halide dispersing agent some or all of the polyvinyl acetate. With the polyvinyl acetates having a vinyl acetate content of less than 5%, water only may be used as the solvent. In the case of polyvinyl acetates having a vinyl acetate content of 59- 71% it is. of course, necessary to also use a small amount of organic solvent with the water employed as the solvent medium. As I have found, however, that the preparation of the silver halide in the dispersing agent with little or no polyvinyl acetate followed by the addition of the most or all of the polyvinyl acetate vehicle, proceeds smoothly and readily, I have ordinarily employed this procedure in preparing the emulsions of my invention.
The hydrolyzed water-permeable polyvinyl propionates or butyrates which are most suitable for use in preparing photographic silver halide emulsions are those having a sufficient permeability to allow development for the emulsion but suflicient insolubility to resist dissolving by the processing baths. These polyvinyl propionates or butyrates may be identified by their similarity in these properties to the polyvinyl acetates having a vinyl acetate content of 59--7l%. Also, vinyl derivatives which are found to have suitable properties for use as carriers in photographic emulsions such as selected from the vinyl dicarboxylates or hydroi'iy esters hydroxy acid esters of vinyl, or the hydrolyzed copolymer of vinyl acetate with a small proporof carboxylates, the 4 tion of another polymerizable compound such as vinyl chloride, styrene, an acrylic acid ester or the like might be employed to form a photographic emulsion as described herein.
I claim:
1. A method of preparing photographic silver halide emulsions which comprises preparing the silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto a protective colloid selected from the group consisting of the polyvinyl lower fatty acid esters having a vinyl acylate content of 0.5-5% and the polyvinyl acetates of 59-71% vinyl acetate content, substantially theremainder being vinyl alcohol.
2. A method of preparing photographic silver halide emulsions which comprises preparing the silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding a protective colloid thereto selected from the group consisting of the polyvinyl acetates having vinyl acetate contents of 0.55% and 59-71%, substantially the remainder being vinyl alcohol.
3. A method of preparing photographic silver halide emulsions which comprises preparing silver halide in an aqueous solution of a water soluble starch acetate and subsequently adding a protective colloid selected from the group consisting of the polyvinyl lower fatty acid esters having vinyl acylate contents of 0.55% and the polyvinyl acetates having vinyl acetate contents of 597l%, substantially the remainder being vinyl alcohol. I
4. A method of preparing photographic silver halide emulsions which comprises preparing silver halide in an aqueous solution of a water soluble lower alkyl cellulose and subsequently adding a protective colloid selected from the group consisting of polyvinyl lower fatty acid esters having vinyl acylate contents of 0.55% and the polyvinyl acetates having vinyl acetate contents of 59'7l substantially the remainder being vinyl alcohol.
5. A method of preparing photographic silver halide emulsions which comprises preparing silver halide in an aqueous solution of a maleic anhydride-vinyl acetate resin and subsequently adding a protective colloid selected from the group consisting of polyvinyl lower fatty acid esters having vinyl acylate contents of 05-23% and polyvinyl acetates having vinyl acetate contents of 59-7l%, substantially the remainder being vinyl alcohol.
, 6. A method of preparing photographic silver halide emulsions which comprises preparing 'a silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto an optical sensitizer and a protective colloid selected from the group consisting of polyvinyl lower fatty acid esters having vinyl acylate contents of 0.5-5% and polyvinyl acetates having vinyl acetate contents of 59-7l%, substantially the remainder being vinyl alcohol.
7. A method of preparing photographic silver halide emulsions which comprises preparing a silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto a polyvinyl acetate having a vinyl acetate content of 0.5-5%, substantially the remainder being vinyl alcohol.
8. A method of preparing photographic silver halide, emulsions which comprises preparing a silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto a polyvinyl acetate having a vinyl acetate content of 59-71%, substantially the remainder being vinyl alcohol. H
9. A photographic silver halide emulsion comprising a finely dispersed silver halide resulting from preparing it in an aqueous solution of a silver halide dispersing agent and a protective colloid selected. from the group consisting of polyvinyl lower fatty acid esters having vinyl acylate contents of 0.5-% and polyvinyl acetates having vinyl acetate contents of 59-71%, substantially the remainder being vinyl alcohol.
10. A photographic silver halide emulsion comprising a finely dispersed silver halide resulting comprising a finely dispersed silver halide re-' sulting from its preparation in an aqueous solution of a silver halide dispersing agent and as the protective colloid a polyvinyl acetate having a vinyl acetate content of 0.5-5%, substantially the remainder being vinyl alcohol.
12. A photographic silver halide emulsion comprising a finely dispersed silver halide resulting from its preparation in an aqueous solution of a silver halide dispersing agent and as a protective colloid a polyvinyl acetate having a vinyl acetate content of 59-71%, substantially the remainder being vinyl alcohol.
13. A photographic silver halide emulsion comprising a finely dispersed silver halide in a mixture of a silver halide dispersing agent. and a polyvinyl acetate selected from the group consisting of the polyvinyl acetates having vinyl acetate contents of 0.55% and of 59-71%, substantially the remainder being vinyl alcohol.
14. A photographic silver halide emulsion comprising a finely dispersed silver halide in a mixture of a water-soluble starch acetate and a polyvinyl fatty acid ester having a vinyl acylate content of 0.5-5%, substantially the remainder being vinyl alcohol. v
WESLEY G. LOWE.
US368661A 1940-12-05 1940-12-05 Photographic silver halide emulsion Expired - Lifetime US2276323A (en)

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2522771A (en) * 1944-11-03 1950-09-19 Gen Aniline & Film Corp Photographic silver halide emulsions
US2541474A (en) * 1946-07-22 1951-02-13 Eastman Kodak Co Preparation of silver halide dispersions and photographic emulsions using polyacrylamide peptizers
US2567750A (en) * 1945-10-25 1951-09-11 Du Pont Light sensitive elements for color photography
US2579016A (en) * 1946-05-17 1951-12-18 Du Pont Preparation of photographic emulsions
US2678884A (en) * 1949-11-18 1954-05-18 Du Pont Photographic silver halide emulsions of synthetic polymers
DE973159C (en) * 1944-11-03 1959-12-10 Gen Aniline & Film Corp Process for making photosensitive photographic emulsions
US2957767A (en) * 1957-12-18 1960-10-25 Monsanto Chemicals Silver halide dispersions
US3253926A (en) * 1962-01-08 1966-05-31 Paul Desire Van Pee Light-sensitive silver halide material containing hydrophobic starch derivatives
US3544327A (en) * 1967-03-03 1970-12-01 Eastman Kodak Co Polymeric fog stabilizers for photographic emulsions

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2522771A (en) * 1944-11-03 1950-09-19 Gen Aniline & Film Corp Photographic silver halide emulsions
DE973159C (en) * 1944-11-03 1959-12-10 Gen Aniline & Film Corp Process for making photosensitive photographic emulsions
US2567750A (en) * 1945-10-25 1951-09-11 Du Pont Light sensitive elements for color photography
US2579016A (en) * 1946-05-17 1951-12-18 Du Pont Preparation of photographic emulsions
US2541474A (en) * 1946-07-22 1951-02-13 Eastman Kodak Co Preparation of silver halide dispersions and photographic emulsions using polyacrylamide peptizers
US2678884A (en) * 1949-11-18 1954-05-18 Du Pont Photographic silver halide emulsions of synthetic polymers
US2957767A (en) * 1957-12-18 1960-10-25 Monsanto Chemicals Silver halide dispersions
US3253926A (en) * 1962-01-08 1966-05-31 Paul Desire Van Pee Light-sensitive silver halide material containing hydrophobic starch derivatives
US3544327A (en) * 1967-03-03 1970-12-01 Eastman Kodak Co Polymeric fog stabilizers for photographic emulsions

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