US3069267A

US3069267A - Photographic emulsions containing hydrolyzed glycogen

Info

Publication number: US3069267A
Application number: US72322A
Authority: US
Inventors: Jr Vaughan Crandall Chambers
Original assignee: EI Du Pont de Nemours and Co
Current assignee: EIDP Inc
Priority date: 1960-11-29
Filing date: 1960-11-29
Publication date: 1962-12-18
Anticipated expiration: 1979-12-18

Description

United States Patent Ofifice This invention relates to photographic gelatino-silver halide emulsions and emulsion layersand to photographic elements embodying the same. More particularly, it relat'es' to such emulsion layers and elements having improved photographic characteristics. more p'articu larly, the invention-relates to a process for increasing the covering power of developed sil ver and improving the maximum density, contrast and effective speed of gelatinosilver halide emulsions.

It is known to add certain chemical compounds, e.g;, heavy metal and noble metal salts to improve'the sensitometric characteristics of photographic gelatino-silver halide emulsions. There is, however, at'the present time, a practical limit to the advantages which can" be obtained by the addition of such compounds without accompanying deleterious effects such as uncontrollable fog and instability on tropical aging. 7

It has been proposed to add to, or replace all or part of the gelatin in a gelatino-silver halide system with various polymeric colloid materials'for various reasons in"- cluding attempts to overcome the well-known disadvanta'ges of gelatin. However, few of these proposals have overcome these disadvantages in a satisfactory manner, and gelatin is still used in most commercial photographic films. In general, when all of the gelatin is. replaced by the synthetic polymers suggested by the prigr art, many of the outstanding photographic and colloid-chemical properties of gelatin are lost.. V 7

An object of this invention is to provide improved photographic gelatino-silver halide emulsions. Another object is to provide such emulsions demonstrating increased covering power of developed silver. Still another object is to-provide a simple and dependable process for making such emulsions. A further object is to-provide a photographic element utilizing such emulsions.v Still further objects will be apparent from the following description of the invention.

Ithas now been found, in accordance with this invention, that gelatino-silver halide emulsions of increased covering power of the, developed silver ande'nhancedproperties can be made by adding to the emulsions an amount of the water-soluble polyglucose, ahydrolyzed:

glycogen having a molecular weight o'f 5,000 to 2,000,000,

so that thehydrolyzed glycogen constitutes 20 to 80 parts and preferably 30v to parts per. 100 parts of gelatin in a" gelatino-silver halide emulsion. The amount of hydrolyzed glycogen. present is based on finished emulsion ready for coating onto a film, paper, metal foil, glass plate.

action. The following procedures can-be usedto produce- :utes. sodium carbonate and cooled. The mixture was conce'n- Patented Dec. 18, 1962 hydrolyzed glycogen of molecular weights satisfactory for "use in the invention:

raocsnuaa A-l Fifty grams of glycogen was added to 1950 ml. of

water in a suitable container and the resulting mixture heated to boiling. To the boiling mixture there was added 8.7 ml. of concentratedhydrochloric acid. The mixture was heated. under reflux conditions for 40 min- The resulting solution was neutralized with solid trated at reduced-pressure on a steam bath to'400 ml. and a precipitateobtained by adding 800 ml.- of a1 :1 mixture of water and ethanol; The precipitate was filtered and washed twice with a mixture of'200 ml.- of water and 400 ml. of ethanol. Upon drying 16.3 grams of a hydrolyzed glycogen was obtained, a 2% aqueous solution of which had a relative viscosity of 1.13 as compared to glycogen which had a relative viscosity of 1.15.

- PROCEDURE A-2 PROCEDURE B-1 The procedurefor Al was repeated except that the refluxtime was .80 minutes, Upon washing and drying, as described in Procedure A L-1911 grams of hydrolyzed glycogen was obtained, a2% aqueous-solution of which h'asa relative viscosity of 1.1-1.

The hydrolyzed glycogen can be incorporated with the gelatino-silver halide emulsion at any stage after precipitation of the silver halide grains in the gelatin but is preferably admixed afterthe final digestion step.

In general, the finished emulsion will contain 20 to parts of the hydrolyzed glycogen per parts of gelatin and the gelatin may be in a ratio to silverhalide of from 1:0.6'to 1:1.5(60 to parts by, weight per 100 parts byweight of gelatin)- The emulsions may, of course, contain small amounts of conventional adjuvants. The final emulsions" show markedly increased silver covering power (e.g'., 10 to 60% greater) over all-gelatin-e rnulsions; To be more specific, with. resp'ect'to covering power for the same quantity of silver halide, large increases in maximum density and contrast can be obtained in the developed image. The covering power of developed silver can be expressed asthe' numerical result of dividing optical density by the grams of silver per square decimeter in the developed image layer. covering power will, of course, vary with the amount of hydrolyzed glycogen used.

The invention is especially suited to gelatino-silver halide emulsions for radiological films, particularly those for medical diagnostic work. However, the invention is by no means limited to any particulartype of gelatinosilver halide emulsion and the'hydrolyzed glycogen may beutilized in any gelatino silve'r halide system to improve its efliciency. The invention is also very useful in theso-called-gr-aphic arts films, i.e., lithographic films. In: all cases when" hydrolyzed glycogen is present in the amounts set forth above, a higher density is obtained from a given amount ofmetallic silver in the developed photographic layer, although the eifect' is more noticeable in large grain silver halide'emulsions' than in smallgra-in emulsions.

The processes of the invention are quite simple" and" consist of merely admixing with the molten or liquefied emulsion after the digestion step an aqueous solution of the hydrolyzed glycogen. As an exemplary procedure, a gelatino-silver iodobromide emulsion useful for X-ray films is prepared by conventional methods. The silver halides are precipitated in gelatin and the resulting dispersion or emulsion ripened. The emulsion is then washed, either after chilling and noodling, or after coagulation by decanting the supernatant liquid. The emulsion is redispersed and then it is digested to bring it to maximum speed. Following digestion, a hydrolyzed glycogen having a molecular weight of from 5,000 to 2,000,- 000 (usually in aqueous solution) is added to the molten emulsion in an amount sufficient to provide the desired ratio of hydrolyzed glycogen to gelatin. The usual final additions, e.g., of hardener, antifogging agents, sensitizing agent and spreading agent, are made and the emulsion is coated on a suitable support and dried in the usual manner. To test the eifectiveness of hydrolyzed glycogen, the element is exposed in a sensitometer according to a procedure based on the American Standard Method for the Sensitometry of Medical X-ray Films PH 2.9-1956.

The sensitometer used in the following examples was equipped with a neutral density /2 step wedge. The density of a selected step, as set forth in the tables, was measured and the quantity of metallic silver per square decimeter was determined by analysis. The density divided by the quantity of silver in grams per square decimeter was taken as an expression of covering power of developed silver.

The invention will now be illustrated further by, but is not intended to be limited to, the following examples. The quantities of hydrolyzed glycogen are given as parts by weight per 100 parts of gelatin in the emulsion.

Example I A high-speed gelatino-silver iodobromide emulsion was made in the usual manner and digested with an organic sulfur compound and gold chloride. It contained approximately 1.6 mol percent of silver iodide and 98.4 mol percent of silver bromide and the ratio of gelatin to silver halide was approximately 1:1. The emulsion was divided into three parts and to each of two portions there was added enough of a 6.7% aqueous solution of the hydrolyzed glycogen product of Procedure A-l above to give the parts by weight per 100 parts of gelatin in the emulsion as indicated in the table below. The remaining portion of emulsion served as a control. The emulsions were coated and dried in the conventional manner. The coatings were exposed in the sensitometer and developed for minutes in a developer of the following composition:

Grams p-N-methylaminophenol hydrosulfate 3.0 Anhydrous sodium sulfite 50.0 Hydroquinone 9.0 Anhydrous sodium carbonate 50.0 Potassium bromide 4.5

Water to make 1,000 ml.

Following development, the films were fixed, washed and dried in the conventional manner. The results of the sensitometric tests and measurements of covering power are shown in the following table:

Example 11 An emulsion was made and treated in the same manner as in Example I except that a 6.7% aqueous solution of hydrolyzed glycogen product oflProcedure A-2 was add- 5 ed in place of the product from Procedure A-l. The results are shown in the following table. The relative coating weights are given to show that the emulsion containing hydrolyzed glycogen was coated at approximately 66% of the coating weight of the control.

Parts of Covering hydrolyzed Relative power of glycogen coating Maximum developed per 100 weight density silver at parts of densities gelatin of 1.41.2

1 (Control) 0 100 1.80 32 2 35.5 66 1. 37 37 It will be seen that, although substantially less silver halide was used in the coatings containing hydrolyzed glycogen, more efiicient use has been made of the developed silver.

Example III An emulsion was made and treated in the same manner as in Example I except that a 6.7 aqueous solution of the hydrolyzed glycogen product obtained from Procedure B-l was added in place of the product added in Example I. Sufiicient quantity was added to give the parts by weight per 100 parts of gelatin indicated in the following table:

Parts of Covering hydrolyzed power of glycogen Maximum developed per 100 density silver at parts of densities gelatin oi 1.4:l=.2

1 (Control) 0 1.80 32 2 An emulsion was made and treated in the same manner as described in Example I except that a 10% aqueous solution of unhydrolyzed glycogen was added in place of the product from A-l. Sufiicient quantity was added to give the parts by weight per 100 parts of gelatin indicated in the following table:

Parts of un- Covering hydrolyzed power of glycogen Maximum developed per 100 density silver at parts of densities gelatin of 1.45:.2

1 (Control) 0 1. 38 33. 7 2 35.5 1.47 32.6 71 1. 52 33.7

It will be seen from the above table that unhydrolyzed glycogen is completely inactive as it shows no improvement in the covering power of the developed silver.

It has been found that the increased covering power of the silver in the developed photographic emulsion layers is not limited to adding the hydrolyzed glycogen to the gelatino-silver halide emulsion layer. The beneficial results can also be attained by incorporating the hydrolyzed glycogen in a gelatin composition to be coated next to a gelationo-silver halide emulsion layer, e.g., in a gelatin sublayer, a separator or light-filtering layer or in an antiabrasion layer. The amount of hydrolyzed glycogen so used can be based on the total gelatin in the same ratio to total gelatin as the ratio recited above to the gelatin.

in the emulsion layers alone.

As will be apparent from the above description, the invention is not limited to the specific quantities of hy drolyzed glycogen as shown in the examples. According to the Whistler and Smart reference, Polysaccharide Chemistry, referred to above, the glycogens of this invention are branched polymers having D-glucose residues linked tat-1,4 except at the branch points where the linkage is tat-1,6. The average length of a branch in a glycogen molecule is either 12 or 18 units per end group depending on the source of the glycogen.

The invention is not limited to photographic gelatinosilver halide emulsions of the silver iodobromide type. The invention may be applied to other gelationo-silver halide emulsions, e.g., gelationo-silver bromochloride emulsions of the lithographic type as well as silver bromide emulsions. This invention is particularly efficacious in photographic emulsions whose average grain size is relatively large. The hydrolyzed glycogens are useful not only with black and white photographic and X-ray emulsions, but with photographic emulsions used in color photography. Suitable emulsions can contain color formers in addition to gelatin and a hydrolyzed glycogen. Examples of useful gelationo-silver halide emulsions and color formers useful therein are disclosed in- Middleton and Jennings US 2,319,426, Dorough US. 2,380,032, Dorough US. 2,380,033 and Woodward and Chu U.S. 2,927,024.

The emulsions may contain any of the well-known optical sensitizing dyes as well as non-optical sensitizers such as sulfur sensitizers containing labile sulfur, e.g., allyl isothiocyanate, allyl diethyl thiourea, phenyl isothiocyanate and sodium thiosulfate, the polyoxyalkylene ethers in Blake et al., US. Patent 2,400,532 and the polyglycols disclosed in Blake et al., U.S. Patent 2,432,549. Other non-optical sensitizers such as amines as taught by Staud et al., U.S. Patent 1,925,508 and metal salts as taught by Baldsiefen, US. Patent 2,540,085 and Baldsiefen et al.,

US. Patent 2,540,086 may also be used. Antifoggants,

e.g., benzotriazole and triazaindenes, can be used as well as the usual hardeners, i.e., chrome alum, formaldehyde, etc.

The emulsion may be coated on any suitable support such as paper or films composed of cellulose esters, e.g., cellulose triacetate, cellulose acetate/butyrate; superpolymers, e.g., polyvinyl chloride (co) vinyl acetate; polyvinyl acetals, e.g., formals, acetals; polystyrene; polyamides, e.g., polyhexamethylene adipamide, and polyesters, e.g., polyethylene terephthalate, polyethylene terephthalate/isophthalate, esters formed by condensing terephthalic acid and dimethyl terephthalate with proplyene glycol, diethylene glycol, tetramethylene glycol or cyclohexane-1,4-dimethano1 (hexahydro-p-xylene alcohol). The vinylidene chloride copolymer-coated oriented polyester films of Alles US. Patent 2,779,684 are especially suitable.

An advantage of the invention is that it provides a simple, dependable and eifective means for providing gelationo-silver halide photographic emulsions of enhanced covering power of developed silver. The efficiency of the resulting developed silver is increased, that is, it can provide greater density pre quantity of metallic silver which results from development.

Another advantage of the invention is that the addition of hydrolyzed glycogen to photographic emulsions tit requires no special technique and can be carried out by the ordinary technician with conventional apparatus Since hydrolyzed glycogens can be added from aqueous solutions, they do not provide the problems of solvent recovery; the resulting modified gelatino-silver halide emulsions can be coated and dried in the conventional coating and drying apparatus which offers commercial advantages. Still further advantages will be apparent from the foregoing description of the invention.

What is claimed is:

1. A photographic silver halide emulsion having improved covering power of developed silver comprising, on a dry basis per 100 parts by weight of gelatin, 20 to 80 parts by weight of a water-soluble hydrolyzed glycogen having an average molecular weight within the range of 5,000 to 2,000,000, and to 150 parts by weight of a light-sensitive silver halide.

2. An emulsion as defined in claim 1 wherein said silver halide is silver iodobromide.

3. A photographic element having improved covering power of developed silver comprising a support and a gelatino-silver halide emulsion layer comprising, on a dry basis per 100 parts by weight of gelatin, 20 to parts by weight of a water-soluble hydrolyzed glycogen having an average molecular weight within the range of 5,000 to 2,000,000, and 60 to 150 parts by weight of a lightsensitive silver halide.

4. A photographic element as defined in claim 3 wherein said silver halide is silver iodobromide.

5. A photographic element having improved covering power of developed silver comprising a support, a gelatino-silver halide emulsion layer and a layer contiguous with the silver halide emulsion layer, the said contiguous layer containing, on a dry basis per parts by weight of gelatin, 20 to 80 parts by weight of a hydrolyzed glycogen, any remaining constituent of the contiguous layer being gelatin.

6. A process for improving the covering power of developed silver in a silver halide emulsion which comprises admixing with a digested gelatino-silver halide emulsion containing, on a dry weight basis per 100 parts by weight of gelatin, 60 to parts by weight of a light-sensitive silver halide, from 20 to 80 parts by weight of a watersoluble hydrolyzed glycogen per 100 parts of gelatin, said hydrolyzed glycogen having an average molecular weight within the range of 5,000 to 2,000,000.

7. A process as defined in claim 6 wherein said silver halide is silver iodobromide.

Press, Inc., New York, 1953, pages 444-45.

Claims

5. A PHOTOGRAPHIC ELEMENT HAVING IMPROVED COVERING POWER OF DEVELOPED SILVER COMPRISING A SUPPORT, A GELATINO-SILVER HALIDE EMULSION LAYER AND A LAYER CONTIGUOUS WITH THE SILVER HALIDE EMULSION LAYER, THE SAID CONTIGUOUS LAYER CONTAINING ON A DRY BASIS PER 100 PARTS BY WEIGHT OF GELATIN, 20 TO 80 PARTS BY WEIGHT OF A HYDROLYZED GLYCOGEN, ANY REMAINING CONSTITUENT OF THE CONTIGUOUS LAYER BEING GELATIN.