US2678884A - Photographic silver halide emulsions of synthetic polymers - Google Patents

Description

Patented May 18, 1954 UNITED STAT .ATENT OFFICE PHOTOGRAPH-Hi] SILVER HALIDE EMUL- SIONS F SYNTHETIC POLYMERS No Drawing.

13 Claims.

This invention relates to halide emulsions.

In the manufacture of photographic silver halide emulsions, which are dispersions of crystalline, light-sensistive silver halides protected by hydrophilic col oids, the most commonly used protective colloid is gelatin. While elatin has many advantages which contribute to its successful use in photographic emulsions, it has a number of undesirable properties. For example, it is brittle, unstable, susceptible to the action or mold, fungi and bacteria, especially under conditions of high humidity, and cannot be processed in warm water unless given special treatment. Furthermore, gelatin is derived from natural sources and hence is subject to considerable variations in its properties. In particular, the properties vary with the source of the raw material and the particular treatment to which it is subjected during isolation. Therefore, gelatin for use in photographic emulsions always requires careful and extensive purification procedures to make it satisfactory for use in this application.

Other polymeric materials have been proposed for use as the protective colloid in photographic emulsions in order to avoid the defects of gelatin. The most promising of these new mate rials are synthetic, hydroxylated polymers containing as recur ing intralinear units the group {photographic silver such as polyvinyl alcohol. However, such synthetic, hydroxylated polymers have the disadvanta e of f ming silver halide emulsions of small pi, -ole else and low photographic speed. Such emulsions have been subjected to conventional ripening processes in attempts to improve their photographic properties. Some of the procedures which have tried involve boiling the emulsion for several hours under acidic conditions, when nitrogenous bases such as ammonia or ethylenediamine present heating has been carried out at moderate temperatures, e. g., sac-cc C. or lower. These treatments, which have based on conventional gelatin emulsion technology, where it has been established that ripening temperatures must be held below 50 0. when an alkaline material is present in order to fogging of the emulsion and hydrolysis of n have not, however, been capable of pro-- s nthetic, hydrcxylated polymer emulsicne with its high photographic speed desired in photo raphic emulsions has apparently retard- Application November 18, 1949, Serial No. 128,254

ed their commercial use in high speed emulsions up to the present time even though such binders, particularly polyvinyl alcohol, have been proposed for many years.

t has now been found that high speed photographic silver halide emulsions which are free from the disadvantages of gelatin emulsions, can be prepared by this invention which involves subiecting to temperatures of above C. lightsensitive silver halides dispersed in a synthetic hydroxyl-containing polymer having a plurality of intralinear groups as recurring units in the presence of a nitrogenous base in concentrations of between 0.1 and 2.5N. Several procedures can be used in carrying out the process of this invention, all of which involve treatment of the emulsions at temperatures of above 80 C. in the presence of the concentration of the nitrogen base specified above. This treatment of the emulsions at unconventionally high temperatures in the presence of the nitrogen base has been found to result in the formation of silver halide/hydroxylated polymer emulsions having the requisite large particle sizes to give high photographic speed.

One method, which involves precipitating the silver halides in the presence of a nitrogen base at high temperature, is especially suitable for the preparation of emulsions containing as the silver halide binder a synthetic, linear hydroxylated polymer containing a, plurality of intralinear groups having a minor amount of acetal substitution. In this process the precipitation of the silver halide is carried out in the presence of a concentration of a nitrogen base preferably ranging from 0.9 to Lill at a temperature of between 86 and 106 C. The precipitation of the silver halide may be carried out in any of several ways, among which are: (a) the simultaneous addition of the soluble silver salt and soluble halide solutions, e. g., an aqueous solution of silver nitrate and aqueous solution or a mixture of ammonium bromide and potassium iodide, to a solution of the synthetic, hydroxyl-containing polymer; (b) the addition of the soluble silver salt solution to a solution containing both the soluble halide and the polyvinyl acetal binder; (c) the addition of soluble halide to the combined silver and synthetic, hydroxyl-containing polymer solutions; and, (d) the addition of the silver solution in portions at difierent temperatures to a solution of a mixture of soluble halide and the synthetic, hydroxylcontaining polymer. In the precipitation procedures just described, the nitrogen base may be included in the silver salt, soluble halide, or hydroxyhcontaining polymer solution. After the precipitation of th silver halide particles is complete, the emulsion is held at a temperature of 80 to 100 C. for a short period to complete the development of the desired silver halide grain size, Periods of time ranging from 1 to 30 minutes are generally sufiicient for such heat treatment but periods up to two hours can be used. After cooling to about 30 C., the emulsion is coagulated, for example, by forcing the emulsion in a fine stream into a aqueous sodium sulfate solution. The coagulum is then washed free of soluble salts after which it is redissolved by stirring it into a mixture of alcohol and water at a temperature of about 75 C. Additional synthetic hydroxyl-containing polymer solution is conveniently added at this time to bring the emulsion to a viscosit suitable for coating on a support such as paper or film. Other finishing ingredients, e. g., triethanolamine and C-cetylbetaine can also be incorporated in the emulsion at this stage.

Another method of carrying out the process of this invention involves the heat treatment of a previously precipitated emulsion. In this process the silver halide is precipitated in a solution of the synthetic, hydroxylated polymer in the presence of 0.9 to IAN nitrogen base at temperatures from about to C., and the resulting precipitate is then subjected to a ripening step at a temperature of between 80 and 125 C., preferably between 90 and 110 C., without removal of soluble salts and nitrogen base, or the addition of other materials. Ripening times ranging from 1 to 30 minutes at such temperatures are usually sufficient to develop silver halide grains of the desired particle size, but ripening times up to ten hours can be used. After ripening is completed, the emulsion is coagulated,

washed, redissolved, and finished as in the preceding embodiment.

In still another exemplary method the silver halide/synthetic hydroxylated polymer emulsion is subjected to the heat treatment in the pres ence of the nitrogen base after the silver halide is precipitated, the emulsion coagulated, and the coagulum washed free of excess soluble salts. The washed coagulum is mixed with an amount of a nitrogen. base, e. g., triethanolamine, ranging between 0.1 and 1.4N based on the total emulsion, and, if desired, a small amount of a surfaceactive agent, e. Ccetylbetaine, and the emulsion digested at temperatures up to 200 C., preferably at 150 to 200 C. In this embodiment of the invention, the lower concentrations of nitrogen base within the limits specified above are preferred. Digestion periods of 1 to 30 minutes at temperatures of 150 to 200 C, are usually surficient to produce silver halide grains of the desired particle size, but when digestion temperatures of 80 to 150 C. are used times up to ten hours are required. After di estion is complete, the emulsion is cooled and brought to the desired coating viscosity by the incorporation of additional synthetic, hydroxylated polymer solution. At this stage the desired finishing agents can also be incorporated in the emulsion.

As evident from the above descriptions of the difierent embodiments of this invention, the process conditions can be varied considerably within the specified limits. The optimum temperature and time to which the silver halide/synthetic hydroxylated polymer emulsion is to be subjected to develop the desired silver halide grain size, how ever, are somewhat interrelated and are also dependent on the concentration of the nitrogen base. In general, heating times ranging from one minute to ten hours can be employed. Usually heat treatments at the higher temperatures within the ranges specified above are carried out for the shorter times and in the presence of the lower concentrations of nitrogen base. By way of illustration, precipitation or ripening steps carried out at to C. in the presenc of 0.9 to IAN ammonia are continued for several hours. However, when temperatures of 90 to C. are employed with the same concentration of ammonia, periods of only 15 to 30 minutes are sufficient and when ammonia concentrations of 2.5N are used still shorter times are sufiicient. At temperatures of to C. and with 0.9 to 1.4N ammonia, ripening periods of 5 to 15 minutes are usually employed. When the coagulated and washed emulsion is subjected to a digestion treatment at 150 to 200 C. in the presence of a nitrogen base in concentrations of 0.1 to lxiN, periods of 1 to 30 minutes are satisfactory, the 30-minute digestion being necessary only with very low concentrations of base, e. g., 0.1 to 0.5N.

The process of this invention has the commercial advantage that it is cap-able of producing a silver halide/synthetic, linear, hydroxylated polymer emulsion having photographic speeds suitable for use as negative-type coatings. The negative-type, hydroxylated polymer emulsions produced by the process of this invention are unique in the photographic art. These emulsions are characterized by having silver halide grains with a root mean square diameter of from 0.6 to 3.0 microns.

The invention is illustrated further by the following examples in which the proportions of the ingredients are expressed in parts by weight unless otherwise specified and in which all radiations which will expose or fog the light-sensitive silver halides are excluded.

EXAMPLE I A solution of a completely hydrolyzed vinyl acetate/ethylene copolymer of mole ration 25:1 (prepared as described in Example 11' of U. S. P. 2,397,866) in aqueous ethanol is prepared in the polymer/ethanol/water weight ratio of 10/10/80. The following solutions are then prepared.

Solution A 3N aqueous silver nitrate solution ml 70 20% aqueous ammonium hydroxide ml 42 Solution B 3N aqueous ammonium bromide solution ml" 74 0.5N aqueous potassium iodide solutlon ml 12 Distilled water m 26 Above-described polymer solution g Solutions A and B are heated to 95 C. and Solution A is added to B with stirring over a period of nine minutes. After precipitation of the silver halide is complete the emulsion is stirred for an additional five minutes at 95 C., then cooled and washed by dialysis (as described in Example I of U. S. application Ser. No. 726,961, filed February 6, 1947, by C. F. Glick) until the conductivity of the emulsion is 120 micromhos. Another 140 grams of the above-described polymer solution is added with stirring to the dialyzed emulsion. To one-half of the emulsion is added six milliliters of a 20% aqueous solution of triethanolamine and 3.5 milliters of a 3% aqueous solution of C-cetylbetaine. The emulsion is finally adjusted to proper coating viscosity by the addition of 10% aqueous ethanol, and then coated on cellulose nitrate film which has previously been given a subcoating of vinylpyridine polymer as described in U. S. P. 2,448,525. When dry, the resulting film is exposed to tungsten light through a step tablet, developed in a solution con taining:

- Grams N,N diethyl p phenylenediamine hydrochloride r 2.5 Sodium sulfite (anhydrous) 10.0 Sodium carbonate (monohydrated) 29.25 Potassium bromide 2.0

Water to make 1.0- liter.

fixed for a period of ten minutes in a 25% sodium thiosulfate solution, washed and dried.

Sensitometric measurements show the emulsion of the above example has about eight times the speed of one prepared from the same ingredients but precipitated at 25 C., and ten times the speed of an unsensitized gelatin print film.

The silver halide grain size of the emulsion of the EXAIVHLE II A photographic emulsion is prepared from the same ingredients and in the same manner as described in Example I except that the precipitation is preformed at 25 C. One-half of the resulting emulsion is placed in a sealed container and heated with stirring at 110 C. for ten minutes. The ripened emulsion is cooled, washed by dialysis as described in Example I to a conductivity of 350 micromhos and finished by the addition of '70 grams of polymer solution and the coating aids as in Example I. The emulsion is coated on film base, exposed and processed as in Example I.

Sensitometric tests show that the emulsion of Example II, ripened at 110 C., has about 20 times the speed as the other half of the emulsion which was finished and coated on film base without the high temperature ripening step.

EXAMPLE III A photographic emulsion containing a polyvinyl alcohol containing a minor amount of acetal substitution as the binder for the silver halide particles is prepared as follows. Fifty grams of a polyvinyl alcohol containing minor amounts of acetal groups of m-[p-(-ethylcarbonato 3 methyl 5 pyrazolyl) -benzamido] benzaldehyde (prepared as described in Example III of U. S. P 2,476,988) is dissolved by heating 20 minutes at 80 C. in 190 milliliters of ethanol and 450 milliliters of water containing two milliliters of KOH solution. The solution is filtered and made up to 667 grams with 30% 6 aqueous ethanol. The following solutions are then prepared:

The solutions are maintained at 25 C. and Solutions A and B are added separately and simultaneously (B leading A slightly) to C with stirring Within a period of eight minutes. Following completion of precipitation the emulsion is stirred for an additional ten minutes at the same temperature. Seventy-five milliliters of ethanol is then added. One-half of the emulsion is placed in a sealed container and heated with stirring at C. for three minutes. Following ripening, 25 milliliters of ethanol is added and the emulsion is washed by dialysis as in Example I until the conductivity is 500 micromhos. One hundred and fifty-four grams of the low-substituted polyvinyl acetal solution is then mixed into the emulsion. To one-half of the emulsion is added 4.2 milliliters of a 20% aqueous solution of triethanolamine and 231 milliliters of a 2% aqueous solution of C-oetylbetaine. The emulsion is then adjusted to suitable coating viscosity and coated on film base as in Example I.

After photographic film coated with the emulsion of Example III is exposed and processor. in Example I except that following development the film is in a solution oonsisting of am to make i liter.

After fixing, film is washed and bleached t on containing 5 grams of potassium ferll oi boric acid, 5 grams of hora and water to mak one liter. After hleaching, the film is Washed, fixed in 25% sodium thiosulfate solution, washed dried. The film then carries a magenta Sensitom tric t... show the rip n a 5GB greater than that of emulsionprepared in the sa. .3 way with the single exception that ripening step at 95 C. 0:1".."ted. The silver halide particles in .pened emulsion of trip e III have a root 1' square diameter icrons; the silver halide grain 'zened in ion is only 0.1 to 6.2 diameter.

EXAMPLE IV eon containing another a m nor amount of astitution cinder for the silver halide 3 is follows. Fifty grams of a low-substituted polyvinyl acetal of m-benzoylspeed or the otograpnic er alsion of Example III to be about 7 acetamidobenzaldehyde (prepared as described in U. S. application Ser. No. 9330, filed February 18, 1948, now U. S. Patent 2,513,190), is dissolved by heating 25 minutes at 80 C. in 165 milliliters of ethanol and 285 milliliters of water. Two milliliters of a 10% aqueous KOH solution is added and heating is continued for five minutes longer after which the solution is cooled and made up to 500 grams with 30% aqueous ethanol. The following solutions are prepared for use in making the silver halide emulsions:

Solution A 3N aqueous AgNOs ml 20 20% aqueous NI-I4OH ml 20 Distilled water ml- 25 Solution B 3N aqueous Nl'liBr ml 22 0.5N aqueous KI ml 4 Distilled water ml- 14 Ethanol ml 25 Solution C Low-substituted polyvinyl acetal solution (described above) g 30 Distilled water ml 45 Ethanol ml 25 Solutions A and B are added separately and simultaneously (B leading A by two parts) to Solution C over a period of is minutes while stirring at 25 C. The emulsion is stirred 15 minutes after the completion of the precipitation and then 50 milliliters of ethanol is added. The emulsion is placed in a sealed container and ripened by stirring at 105 C, for 7 minutes, cooled and washed by dialysis as in Example I. At the completion of the dialysis most of the emulsion has coagulated and has settled out. The coagulum is redissolved by heating 15 minutes at 65 C. with 150 milliliters of 25% aqueous ethanol, then an additional 100 grams of the low-substituted polyvinyl acetal solution is added and heating is continued 15 minutes longer. The emulsion is then prepared for coating and coated on film base as in Example I.

The dry film is exposed and processed as in Example III, giving a yellow image.

Sensitometric measurements show the speed of the emulsion to be about nine times that or an emulsion prepared from the same ingredients and in the same manner with the single exception that the ripening at 105 C. is omitted. The silver halide particle size of the ripened emulsion of Example IV is 1.48 microns root mean square diameter; whereas, the grain size of the unripened emulsion is only 0.23 micron root mean square diameter.

EXAMPLE V A photographic emulsion having still another partial acetal of polyvinyl alcohol as the silver halide binder is prepared by a procedure similar to that described in Example IV. Thirty grams of a low-substituted polyvinyl acetal of m-('- methyl-salicylamido)benzaldehyde (prepared as described in U. S. application Ser. No. 29,921, filed May 28, 1948, U. S. Patent 2,538,257) is dissolved by stirring at 80 C. for 25 minutes in 90 milliliters of ethanol and 210 milliliters of water. To this solution 9.5 milliliters of 10% aqueous KOH solution is added and the heating continued for an additional five minutes. The resulting solution is made up to 300 grams by the addition of 30% aqueous ethanol. The photographic emulsion is prepared from the same solutions described in Example IV with the exception that the polyvinyl acetal solution of Solution C in Example IV is replaced with the same quantity or" the above-described polyvinyl acetal solution. At the completion of the precipitation milliliters of ethanol is added and the emulsion placed in a sealed container and ripened by heating for 7 minutes at 105 C. with stirring. Fifty milliliters of ethanol is added after the ripening step and the emulsion is washed by dialysis as in Example I. The emulsion coagulates, and the coagulum is redissolved as described in Example IV, then finished and coated on film base in the manner described in that example. Exposure to light and processing as in Example IV yields a film having a cyan image.

Sensitometric measurements of the film of the above example show it to have about 450 times the speed of a film prepared from an unripened emulsion. The silver halide grain size in the emulsion of Example V is 0.65 micron root mean square diameter. The grain size of the unripened emulsion is only 0.11 micron root mean square diameter.

EXAMPLE VI The following solutions are prepared:

Solution A 3N aqueous AgNOg ml. 35 20% aqueous ammonium hydroxide ml. 30

Solution B 3N aqueous NIiiBr ml. 37

0.5N aqueous KI ml. 6

Distilled water ml. 22

Solution C 10% aqueous polyvinyl alcohol (completely hydrolyzed low molecular weight polyvinyl acetate) solution g. 20

Distilled water ml.

Solutions A and B are added separately and simultaneously (B leading A by two parts) to Solution C at 25 C. while stirring over a period of six minutes. The emulsion is then ripened for 15 minutes at C. in a sealed container. Following ripening, 100 grams of a 10% solution of a completely hydrolyzed high molecular weight polyvinyl acetate is added, and the emulsion is washed, prepared for coating as in Example I, and coated on film base. After drying, the film is exposed and processed as in Example I.

The film of Example VI has a photographic speed of 50 to 100 times that of a film coated with an emulsion prepared with the same type of polyvinyl alcohol binder but ripened under acidic conditions. The size of the silver halide grains in the emulsion of Example V1 is 2.0 microns root mean square diameter. Furthermore, an emulsion prepared in the same manner as Example VI with the single exception that the ammonia is omitted from the silver nitrate solution has a silver halide grain size of only 0.04 micron root mean square diameter and this grain size remains unchanged on ripening at 100 C. for 15 minutes.

EXAMPLE VII A photographic emulsion is prepared by precipitating silver halide at a high temperature in the polyvinyl acetal binder of Example IV. Ten grams of the low-substituted polyvinyl acetal of m-benzoyl-acetamidobenzalydehyde is stirred at 80 C. for 15 minutes in a mixture of 24 milliliters of ethanol, 171 milliliters of Water, and 1 milliliter of 7.5% aqueous NaHCOs solution. The following solutions are then prepared for use in forming the emulsion:

Solution A 3N aqueous AgNOa ml. 29 aqueous NHiOH ml. 29 Water ml. 7

Solution B 3N aqueous NI-I4Br ml. 31 0.5N aqueous KI ml. 2 Water ml. 32

Solution C Low-substituted polyvinyl acetal solution described above) g. 103 Ethanol ml.

Solutions A and B are run separately and simul tanecusly into Solution C while stirring at 95 C. The emulsion is maintained at 95 C. for ten minutes after completion of precipitation. The emulsion is then coagulated by pumping it through a capillary into 15% aqueous NazSO4 solution. The coagulum is broken up and washed in running water for one hour, after which it is redissolved by stirring at 75 C. for 15 minutes with 25 milliliters of ethanol made up to 100 milliliters with water. The remainder (103 grams) of the polyvinyl acetal solution is then added, and heating, is continued for 15 minutes more. The emulsion is finished and coated on film base as described in Example IV. After drying, the photographic film is exposed and, processed as in Example IV. Sensitometric tests of the resulting film show that the emulsion is approximately 1,000 times as fast as one prepared from the same ingredients and in a similar man.- ner with the single exception that the precipitation of the silver halide was carried out at 20 C.

The examples have illustrated the process of this invention by referring to certain hydroxylated' polymers as the polymeric binders for the silver halide particles; however, other synthetic, linear, hydroxylated polymers can beused. Synthetic hydroxylated polymers which are operable include film-forming polymers which contain as the predominant hydrophilic group a plurality of recurring vinyl alcohol,

units. Polyvinyl alcohol and its partially substituted esters, ethers and acetals are especially useful polymers of this type. Polyvinyl alcohol is a tough, water-white, polymeric material which is soluble in water. The more highly polymerized varieties are soluble in hot water, and the lower polymers are soluble in cold water. They areusually prepared by hydrolysis of polyvinyl esters, such as polyvinyl acetate, and polyvinyl'isobutyrate, etc. The partially hydrolyzed esters which contain a large numberof recurring vinyl alcohol,

l *CHP-CHOH chloride and styrene; and monoolefins, e. g., ethylene. Hydrolyzed ethylene/vinyl acetate copolymers are especially useful types of such copolymers. Hydrolyzed ethylene/vinyl acetate copolymers containing less than 10 ethylene are hydrophilic and form highly suitable polymeric binders in the process of this invention.

An indicated above the low-substituted polyvinyl acetals, i. e., polyvinyl alcohol having less than about 13% of its hydroxyl groups substituted as acetals, are especially preferred as the synthetic, hydroxyl-containing polymer binders of this invention. These acetals can be made by acetalization ofpolyvinyl alcohol and its completely hydrolyzed carboxylic esters. Examples of such acetals are polyvinyl alcohols whose hydroxyl groups are partially substituted as acetals ,by acetaldehyde, benzaldehyde, 2-thiophene aldehyde, in-acetamidobenzaldehyde, m-aminobenzaldehyde, succinaldehydic acid, butyraldehyde, and p-diethylaminobenzaldehyde.

Synthetic, hydroxylated polymers containing small amounts of color-forming acetal groups are especially suitable as the silver halide binder. These are more precisely defined as essentially colorless, synthetic, linear, hydroxylated polymers, 0.75 to 7.5% of whose hydroxyl groups are substituted as acetals by color-former nuclei with the structure Where X is a member of the group consisting of hydroxyl and primary and secondary amino radicals, 11. having a value of 0 or 1, and which may be 0.1 to 5.2% substituted as acetals by aldehydes containing carboxylic or sulfonic acid groups, said polymers containing at least 12.5 but less than 49 hydroxyl groups for every chain atoms and between 1 and 35 color-forming groups for each 100 chain atoms and a polymer chain in excess of 200 carbon atoms. In addition to the specific polyvinyl acetals of this type mentioned in Examples III, IV, V and VII other polyvinyl acetal color-formers having a maximum of 7.5% of the hydroxyl groups substituted as acetals by the color-former nuclei which can be used include polyvinyl acetals of m-[p-(5-benzoxy-3-methyl- 1 pyrazolyl)benzamidolbenzaldehyde, as described in U. S. application Ser. No. 682,137, U. S. Patent 2,476,988; m-(p-chlorobenzoylacetamido)benzaldehyde, and 4-methyl-3-(benzoylacetamido)benzaldehyde, as described in U. S. ap.- plication Ser. No. 9330, U. S. Patent 2,513,190; and other m-(methylsalicylamido)benzaldehydes, as described in U. S. application Ser. No. 25,921, U. S Patent 2,538,257.

The light-sensitive silver salts mentioned in the examples are mixed crystals, i. e., iodobromides obtained from silver bromide and silver iodide. However, other light-sensitive silver salts may be employed if desired. The silver halides, e. g., silver chloride, silver bromide, and silver iodide, 01' mixturesof any of these, or mixed crystals containing two or more of these salts, are especially suitable.

In addition to the cellulose nitrateiilm base mentioned specifically in the examples as the support for the emulsions of this invention, other common photographic supports can be used if desired. For example, other cellulose derivatives, e. g., cellulose acetate, cellulose acetate butyrate, cellulose propionate, cellulose ethers, polyamides, polyvinyl chloride, polyvinyl acetal, paper, glass, metals, etc., can be used as supports for the emulsions;

The examples have illustrated the process of this invention by the use of ammonia as the preferred nitrogen-containing base which must be present during the high temperature treatment of the silver halide emulsions. However, other nitrogen bases which can act as silver solvents by forming complexes with the silver ion can also be used. Thus, ammonia and amines, including primary, secondary, tertiary, acyclic, cyclic, heterocyclic, mono, and polyamines can be used. EX- amples of specific operable amines include methylamine, ethylamine, diethylamine, triethylamine, benzylamine, triethanolamine, ethylenediamine, propylenediamine, cyclohexylamine, 2- methyl-cyclohexylamine, pyridine, piperidine, and morpholine.

The photographic emulsions of this invention may also contain the usual sensitizers such as oyanines and the carbocyanine salts and bases commonly used to extend the sensitivity of photographic emulsions.

The process of this invention has the great advantage over the hitherto known methods for producing photographic emulsions having synthetic, hydroxylated polymer binders of being capable of producing such emulsions which have the high speeds desired for fast photographic films, i. e., negative emulsions. Furthermore, the emulsions of this invention do not possess the previously mentioned disadvantages of conventional gelatin emulsions. The step of heating the synthetic, hydroxylated polymer/silver halide emulsion to the unusually high temperatures herein specified in the presence of a nitrogen base in the specified concentrations, makes possible the production of high-speed emulsions by development of suiiiciently large silver halide grain size. Processes in which hydroxylated polymer emulsions are heated at high temperatures in the absence of the nitrogen base, or heated to the moderate temperatures of the gelatin emulsion art in the presence of a nitrogen base, are not capable of producing the necessary silver halide grain size for a truly rapid emulsion. For example, an emulsion containing the low-substituted polyvinyl acetal of Example VII precipitated at 85 C. has particles having a root mean square diameter of 0.46 micron; whereas, the particles in a similar emulsion precipitated at 70 C. have a root mean square diameter of 0.22 micron and the particles in another similar emulsion precipi tated at 55 C. have a root mean square diameter of only 0.16 micron.

The synthetic, hydroxylated polymer/silver halide emulsions of this invention are useful for all applications in which gelatin/silver halide photographic emulsions are normally used, i. e., as light-sensitive coatings on paper, glass, films, etc., including both positive and negative types of film. The emulsions of this invention having a silver halide grain size of between 0.6 and 3 microns root mean square diameter are especially suitable as high-speed emulsions for negativetype films.

As many widely different embodiments of this invention can be made without departing from the spirit and scope thereof, it is to be understood that the invention is not to be limited except as defined by the claims.

What is claimed is:

l. A process for increasing the speed of photographic silver halide emulsions which comprises subjecting an aqueous dispersion of light sensitive silver halides in a synthetic hydrophilic i2 hydroxyl-containing polymer having a plurality of recurring intralinear groups to a temperature between and 200 C. in the presence of a nitrogenous base which forms a complex with a silver ion and acts as a silver solvent and is taken from the group con sisting of ammonia, rimary, secondary and tertiary aliphatic amines, cycloaliphatic amines, pyridine, piperidine and morpholine in a concentration of between 0.1 and 2.5N while excluding radiations which will expose the light-sensitive silver halides.

2. A process as set forth in claim 1 wherein said polymer is a low-substituted polyvinyl acetal wherein less than 13 percent of the hydroxyl groups have acetal substitution.

3. A process as set forth in claim 1 wherein said polymer is a hydrophilic hydrolyzed ethylene/vinyl acetate copolymer.

4. A process as set forth in claim 1 wherein said polymer is polyvinyl alcohol.

5. process for increasing the speed of photographic silver halide emulsions which comprises precipitating light-sensitive silver halides in an aqueous dispersion of a synthetic hydrophillc hydroxyl-containing polymer having a plurality of recurring intralinear I -omono11 groups at a temperature between 80 and C. in the presence of a nitrogenous base which forms a complex with a silver ion and acts as a silver solvent and is taken from the group consisting of ammonia, primary, secondary and tertiary aliphatic amines, cycloaliphatic amines, pyridine, piperidine and morpholine in a concentration of between 0.9 and 1.4N While maintaining the mixture at such temperatures for a period of one minute to two hours.

6. A process for increasing the speed of photographic silver halide emulsions which comprises precipitating light-sensitive silver halides in an aqueous dispersion of a synthetic hydrophilic hydroxyl-containing polymer having a plurality of recurring intralinear groups and then heating the resulting aqueous silver halide dispersion to a temperature between 80 and C. in the presence of a nitrogenous base which forms a complex with a silver ion and acts as a silver solvent and is taken from the group consisting of ammonia, primary, secondary and tertiary aliphatic amines, cycloaliphatic amines, pyridine, piperidine and morpholine in a concentration of between 0.9 and 1.4.N for a period of one minute to ten hours while excluding radiations which will expose the light-senitive silver halides.

'7. A process as set forth in claim 6 wherein said polymer is a hydrophilic hydrolyzed ethylene/vinyl acetate copolymer.

8. A process as set forth in claim 6 wherein said polymer is polyvinyl alcohol.

9. A process as set forth in claim 6 wherein said polymer is a low-substituted polyvinyl acetal wherein less than 13 percent of the hydroxyl groups have acetal substitution.

10. A process for increasing the speed of photographic silver halide emulsions which comprises precipitating light-sensitive silver halides in an aqueous dispersion of a synthetic hydrophilic hydroxyI-containing polymer having a plurality of recurring intralinear OHz-( lHOH groups, coagulating the silver halide emulsion of said polymer, washing the coagulum and heating an aqueous dispersion of the washed coagulum to a t'emperature between 80 and 200 C. in the presence of a nitrogenous base which forms a complex with a silver ion and acts as a silver solvent and is taken from the group consisting of ammonia, primary, secondary and. tertiary aliphatic amines, cycloaliphatic amines, pyridine, piperidine and morpholine in a concentration of between 0.1 and 1.4N for a period of one minute to ten hours while excluding radiations which will expose the light-sensitive silver halides.

11. A process as set forth in claim 10 wherein said polymer is a low-substituted polyvinyl acetal wherein less than 13 percent of the hydroxyl groups have acetal substitution.

12. A process as set forth in claim 10 wherein said polymer is a hydrophilic hydrolyzed ethylene/vinyl acetate copolymer.

13. A process as set forth in claim 10 wherein said polymer is polyvinyl alcohol.

References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,179,239 Wilmanns et al Nov. 7, 1939 2,211,323 Fordyce Aug. 13, 1940 2,276,323 Lowe Mar. 17, 1942 2,311,059 Lowe Feb. 16, 1943 2,358,836 Swan Sept. 26, 1944- 2,376,371 Lowe May 22, 1945 2,414,207 Lowe Jan. 14, 1947 2,414,208 Murray Jan. 14, .1947 2,415,381 Woodward Feb. 4. 1947 2,448,534 Lowe et a1 Sept. 7, 1948 2,499,097 Howk et a1. Feb. 28, 1950 OTHER REFERENCES Mees, Theory of the Photographic Process, page 51; MacMillan Company, 1942.

Claims (1)

1. A PROCESS FOR INCREASING THE SPEED OF PHOTOGRAPHIC SILVER HALIDE EMULSIONS WHICH COMPRISE SUBJECTING AN AQUEOUS DISPERSION OF LIGHTSENSITIVE SILVER HALIDES IN A SYNTHESIC HYDROPHILIC HYDROXY-CONTAINING POLYMER HAVING A PLURALITY OF RECURRING INTRALINEAR