US2253078A

US2253078A - Photographic silver halide emulsion

Info

Publication number: US2253078A
Application number: US349295A
Authority: US
Inventors: Wesley G Lowe
Original assignee: Eastman Kodak Co
Current assignee: Eastman Kodak Co
Priority date: 1940-08-01
Filing date: 1940-08-01
Publication date: 1941-08-19
Anticipated expiration: 1958-08-19

Description

Patented Aug.-19,

PH OTOGRAPHIO SILVER HALIDE EMULSION Wesley G. Lowe, Rochester, N. Y., assignor to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey No Drawing. Application August I, 1940, Serial No. 349,295

9 Claims.

This invention relates to photographic silver halide emulsions in which a polyvinyl propionaldehyde acetal or a polyvinyl butyraldehyde acetal is employed as the protective colloid tor the silver halide therein.

Gelatin has ordinarily been employed as the protective colloid tor the light-sensitive silver halides in photographic emulsions due to its ability to hold these salts in suspension. its good water permeability, its insolubility in photographic developing solutions at ordinary temperatures and its ability to form a thin coating of the lightsensitive silver halide emulsion upon a film support. Various other materials have been suggested for use as the protective colloids in photographic emulsions but in mostinstances the suggested materials haveevidenced inferiority in one or more of the properties enumerated compared with gelatin. For instance, cellulose esters, such as cellulose nitrate, have been suggested as carriers for silver salts in photographic emulsions. The emulsion formed, however, when dry, is none too permeable to developing solution and, therefore, cellulose nitrate has not been successful with the conventional developing and fixing baths. Another disadvantage of cellulose nitrate is its insolubility in solvent mixtures-containing appreciableamounts of water. This prevents the use of the water-soluble salts which are now ordinarily employed in forming light-sensitive photographic emulsions.

Various colloidal materials have been mentioned in this connection. However, many of those suggested are deficient for some reason or another, suchas lack of good water permeability, 4

varies in properties from time to time and to obtain it in a highly refined condition, such as is desirable for photographic purposes, requires considerable care. One object of my invention is to provide carriers or protective colloids for light-sensitive silver halides which can be employed instead of gelatin for photographic emulsions. Another obiect of my invention is to provide a carrier for silver halideln photographic emulsions that combines suiilcient permeability for processing with sufficient hardness to withstand the mechanical action in the processing baths. A further object of my invention is to-provide a synthesized rather than a natural product for use as the protective colloid in photographic emulsions. Other objects will appear from a further perusal of this specification.

In its broader aspects, my invention comprises the use of polyvinyl propionaldehyde acetals of approximately 45-60% vinyl alcohol content and polyvinyl butyraldehyde acetals of approximately -80% vinyl alcohol content for the making of photographic silver halide emulsions in place of gelatin. The acetals listed exhibit the best per-,

meability in the higher parts of the vinyl alcohol content ranges given. For instance if an ordinary photographic fixing bath is used the propionaldehyde acetals of 50-60% and the butyraldehyde acetals of -80% vinyl alcohol content are preferred. These acetals are particularly suitable for emulsions for making photographic paper. For acetals in the lower part of the vinyl alcohol content range it is preferred that a fixmgbath be used having good penetrating ability such as could be prepared by the adding of potassium cyanide to the fixing bath.

The following examples illustrate the preparation of acetal resins useful in preparing emulsions in accordance with my invention:

Example A Example B A solution of parts of polyvinyl alcohol in 2000 parts of water was mixed with 50 parts of concentrated hydrochloric acid and 25 parts'of propionaldehyde. The resin formed was separated from the liquid and was washed in water at 60 C, until free of acid. The vinyl alcohol content of the resin was 54.5%.

The vinyl alcohol contents of the resins for use in my invention may be varied by varying the proportion of propionaldehyde or butyraldehyde employed in making them. Polyvinyl propionaldehyde acetals and polyvinyl butyraldehyde acetals having the vinyl alcohol content described, have the ability to hold silver halide in suspension and the emulsions prepared therewith'may be easily coated out upon a support, such as paper, upon which it readily sets and dries to a hard, scratch-resistant emulsion layer. This emulsion'layer may be treated with developing and fixing baths and subsequently washed thoroughly with water without dissolving.

The propionals or butals. which are useful in my invention, are those in which the propionaldehyde and butyraldehyde content of the acetal comprises substantially all of thealdehyde content thereof. It is preferred that there be no other aldehyde present and at the most no more than of the aldehyde content be other than propionaldehyde and butaldehyde. The. acetals, which may be employed in my invention, may be prepared by reacting propionaldehyde or 'butyraldehyde or their mixture with polyvinyl alcohol or they may be prepared by the hydrolysis of substantially all of the acetyl from polyvinyl acetate and reaction of part of theseformed hydroxyl groups with propionaldehyde, butyraldehyde or their mixture. With propionaldehyde or butyraldehyde acetals having a hydroxyl content above the range specified herein, the emulsions are either undesirably soft or even soluble in the photographic processing baths which are necessary in processing the mulsion. I have found that the acetals within the range specified have a permeability and hardness which makes those materials very desirable for use as a protective carrier of photographic emulsions.

The photographic emulsions of my invention may be prepared-,by a process involving first dispersing silver halide in a polyvinyl propionaldehyde or butyraldehyde acetal resin as described, such as by running aqueous solutions of silver nitrate and an alkali metal halide withstirring into a solution of the resin. As the resin is not soluble in water alone, some organic solinto an aqueous solution oi the resin, it is often times desirable to disperse the silver halide in some silver halide dispersing agent and subsequently mix the silver halide dispersion. with an coated on paper or upon a transparent base, such as cellulose ester film base, or glass plates to form what is normally known in the art as photographic film or photographic plates. The silver halide portion of the emulsion is ordinarily prepared by reacting together a water solution of silver nitrate and an aqueous solution of an alkali metal bromide, chloride or iodide or a mixture of any of these. The precipitation is carried out under agitated conditions so that the particle size of the precipitate is minute.

Some of the silver halide dispersing agents which may-be employed, if their use is desired, aresome of the water-soluble synthetic resins, such as the co-polymer of maleic anhydride and vinyl acetate or its derivatives. water-soluble natural resins, such as gum arabi'c or carbohydrate derivatives. such as water-soluble starch acetate or ethanolamine cellulose acetate. The co-polymer of maleic anhydride and vinyl acetate and its derivatives may be prepared in accordance with the process described in U. 5. Patent No. 2,047,398 of I. G. Water-soluble starch acetate is a commercial material and may be obtained from the Niacet Chemical Company or under the trade name "Accotte" from the Doe and Ingalls Company. The ethanolamine cellulose acetate may be prepared by reacting cellulose acetate, which has been hydrolyzed to a low acetyl content such as 22%. with p-toluene sulfonyl chloride and pyridine to form a cellulose acetate-' p-toluene sulfonate which is then reacted with an 'ethanolamine. These compounds and their preparation arethe invention of Kenyon and Reynolds and are described and claimed in their application Serial No. 349,222 filed of even date. The photographic silver halide emulsions of my invention may be sensitized in the same manner as are silver halide emulsions generally. This is ordinarily accomplished with my emulsions by thoroughly incorporating a small amount of sensitizing dye after the emulsion is prepared. Examples of sensitizers, which may be employed in the emulsions described herein, are the cyanines or the sensitizing dyes disclosed in the following patents: U. S. 2,078,233, Brooker, April 27, 1937- U. S. 2,166,736. White et 'al., July 18,1939 U. 8. 2,186,608, Keyes, Jan. 9, 1940. U. 8. 2,165,339, Brooker,.July 11, 1939.

The following examples illustrate my invention: m

Example I A solution or a polyvinyl propionaldehyde acetal resin containing 54.5% vinyl alcohol, was prepared by dissolving the resin in a :30 mixture of ethanol and water so asto give a concentration of 4.8%. 39 grams of this solution, diluted aqueous solution of the resin. 1 have found that tographic silver halide emulsionsadapted to be with 20 cc. of water and 20 cc. of acetone, was heated to 8013. The following solutions, designated A and B, were added simultaneously over a period of three minutes accompanied by rapid Example II A solution of a polyvinyl butyraldehydeacetal resin containing 75.2% vinyl alcohol, was prepared by dissolving it in a mixture oi equal parts Example f 50 cc. of 1 a 2% solution of gum arabic in water was heated to 80 F. and solutions Aand B were added simultaneously over a period of three minutes with rapid stirring. Polyvinyl butyraldehyde acetal resin and ethyl cellosolve were next added in the same manner as described in the preceding example. The emulsionwas of ethanol and water to form a 6% solution. 10

grams of this solution was diluted with cc. of water and cc. of acetone and was heated to 80 F. Solutions corresponding to those desigmultaneously over a period of three minutes with rapid stirring. When half of A and oi! B had been added, 10 cc. of acetone was poured into the emulsion while continuing the addition of A and of B. At the end of the threeminutes, 65 grams of the solution ofthe resin, prepared original ly, was'thoroughly incorporated. The emulsion was sensitized by incorporating 2mg. oi. 2,3- diethyl-4'-methyloxathiazolocarbocyanine iodide. The emulsion was coated on paper and dried. On processing in the conventional baths, this emulsion was found to give good results both as to physical properties and photographic quality.

. Example I]! A solution of a polyvinyl butyraldehyde acetal resin, containing 58% vinyl alcohol, was prepared by dissolving the resin in a 54:46 mixture of ethanol and water to a concentration of 5.7%. grams of this solution was diluted with 30 cc.

of .water and 30 cc. of acetone and heated to 80 F. The following solutions, designated C and D, at a temperature of 80 F. were added simultaneously over a period of three minutes with rapid stirring.

C. 10 on. of 50% silver nitrate in water. D. 16 cc. of 40% potassium bromide and A; cc. of

25% potassium iodide in water.

During the addition of solutions C and D, 10 cc. of acetone was added also. Them-130 grams of the solution of the resin was diluted with 50 cc. of water and 50 cc. of acetone and this was added to the emulsion. The emulsion was then heated for 20 minutesat C. and was washed by pouring into water. The excess water was pressed out and the emulsion was dissolved in a mixture of cc. of water, '75 cc. of acetone and 20 cc. of ethyl cellosolve. It was sensitized with 2 mg. of 2,3-'-diethyl-4'emethyloxathiazolocarbocyanine iodide. The emulsion was coated onto paper and also onto plates forming photographic paper and plates respectively.

Example IV '50 cc. of a 1% solution of diethanolamine cell5 nated as A'and B in Example I were added silulose acetate in water was heated to 80 F. and

sensitized with 2 mg. of 2,3-diethyl-4'-methyloxathiazolocarbocyanine iodide. The resulting emulsion was coated on paper, and dried and gave excellent results on processing.

Example VI 2 grams of the co-polymer of maleic anhydride and vinyl acetate was dissolved in 50 cc. of water and heated to F. Solutions A and B were added simultaneously thereto over a period of three minutes with rapid stirring. grams of a 6% solution of polyvinyl butyraldehyde acetal resin containing 75.2% vinyl alcohol in the molecule, dissolved in a mixture of equal parts of ethanol and water, was added followed by the addition of 10 cc. of ethyl cellosolve. The emulsion was sensitized with 2 mg. of 2,3'-di-- ethyl -.4' methyloxathiazolocarbocyanine iodide. Photographic paper was formed therefrom by coating out onto paper and drying.

Example VII Silver halide was precipitated in a solution of the co-polymer of maleic anhydride and vinyl acetate, as described in the preceding example. 100 grams of a 4.8% solution of polyvinyl propionaldehyde acetal resin containing 54.5% vinyl alcohol dissolved in a mixture of 70 parts oi ethanol and 30 parts of water, was added. The emulsion was sensitized, coated out on paper and dried as described in the preceding example.

As, illustrated by the examples the acetyl resins employed in accordance with my invention are substantially entirely composed of polyvinyl alcohol and polyvinyl acetal, although the presence of a small proportion of polyvinyl ester is not deleterious.

The termv silver halide dispersing agent as used herein is to be understood as referring to any material which (1) in dilute aqueous solution has the power of preventing the agglomerationof particles of silver halide when they form (2) is soluble either in water alone or in a mix-" 7 ture of a large proportion of water with an organic solvent (3) has the power of holding'silver halide in suspension (4) is compatible with the polyvinyl propionaldehyde acetal resin employed and, for the best results, (5) should be sufliciently permeable to improve the permeability of the emulsion.

I claim:

1.A light-sensitive photographic emulsion comprising a silver halide and a carrier therefor selected from the group consisting of the or butyraldehyde I proximately48-60% and the polyvinyl butyralselected trom the group consisting of the polyvinyl propionaldehyde acetals having a combined vinyl alcohol content of approximately 60-60% and the polyvinyl butyraldehyde acetals having a combined vinyl alcohol content oi approximately 70-80%.

4. A light-sensitive photographic emulsion comprising a silver halide and a polyvinyl propionaldehyde acetal having alcombined vinyl alcohol content of 50-60%.

6. A light-sensitive photographic emulsion comprising a silver halide and a polyvinyl butyr-.

aldehyde acetal having a combined vinyl alcohol content of 70-80%.

6. A met/nod of preparing a light-sensitive photographic emulsion which comprises dispersing silver halide in a protective colloid selected from the group consisting of the polyvinyl propionaldehyde acetals having a combined. vinyl alcohol content of approximately 46-80% and 26 the polyvinyl butyraldehyde acetals having a comlained vinyl alcohol content 0! approximately 60-8 r. A method of preparing s light-sensitive photographic silver halide emulsion which comprises preparing the silver halide in an aqueous photographic silver halide emulsion which comprises preparing the silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto as a protective colloid an aqueous solution ot a polyvinyl propionaldehyde acetal having acombined vinyl alcoh content of 60-60%.

0. A method oi preparing a light-sensitive photographic silver halide emulsion which comprises preparing the silver halide in an aqueous solution of a silver halide dispersing agent and subsequently adding thereto as a protective colloid an aqueous solution of a polyvinyl butyraldehyde acetal having a vinyl alcohol content WESLEY G. LOWE.