Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.


  1. Advanced Patent Search
Publication numberUS3672899 A
Publication typeGrant
Publication dateJun 27, 1972
Filing dateNov 2, 1970
Priority dateNov 2, 1970
Publication numberUS 3672899 A, US 3672899A, US-A-3672899, US3672899 A, US3672899A
InventorsArchambault Jean-Paul C, Holmes William S
Original AssigneeItek Corp
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
High contrast photographic media
US 3672899 A
Abstract  available in
Previous page
Next page
Claims  available in
Description  (OCR text may contain errors)

United States Patent Office r 3,6 Patented June 27, 1972 3,672,899 HIGH CONTRAST PHOTOGRAPHIC MEDIA Jean-Paul C. Archambault, Nashua, NH, and William S. Holmes, Graniteville, Mass., assignors to Itek Corporation, Lexington, Mass. N Drawing. Filed Nov. 2, 1970, Ser. No. 86,376 Int. Cl. G03c 1/00, N28 US. CI. 96-88 25 Claims ABSTRACT OF THE DISCLOSURE The use of arylmercuric compounds provides improved photographic properties to photosensitive materials, particularly in improving the sensitometric properties of photographic images. Such images show markedly higher gamma values. The arylmercuric compounds are especially effective in so-called low-content silver halide film, especially those containing very thin photosensitive layers.

Field of the invention This invention relates to the field of photographic media and photographic chemistry.

It has now been discovered that the presence of an arylmercuric compound in the photosensitive layer of a photographic medium substantially improves the photographic efliciency particularly as to image density and contrast. The invention embraces the use of photosensitive materials which are developable to visible images, after photoexposure, by reduction of metal ions or metal compounds to the free metal which forms the visible photographic image. The improvement is especially efiective in media of which the photosensitive material is a photoconductor or silver halide. In the latter type of media, a particularly preferred form of the invention resides in the use of arylmercuric compounds in low content silver photosensitive layers, particularly in so-called thin photosensitive layers. Such low-content silver, thin photosensitive layers and media comprising such layers are described fully in commonly-assigned, copending US. patent application Ser. No. 45,927, filed June 12, 1970, the disclosure of which is fully incorporated herein by reference.

While the mechanism by which the present invention functions is not completely understood, it is probable that some interaction of the added arylmercuric compound and the photosensitive material occurs during photoexposure. The applicants do not wish to be bound to any particular theory regarding the observed phenomenon but it is apparent that the effect is attributable to the presence of the arylmercuric compound in the photosensitive layer during the photoexposure step since the addition of the arylmercuric compound, after photoexposure, e.g. during photoprocessing, does not improve the sensitometric characteristics of the resulting image. Consequently, it is believed that, in some unknown manner, the arylmercuric compound is affected during the photoexposure step, either to interact with the photosensitive material or to form, itself, some spices of active sites or seeds, or both of these, which accounts for the high gamma values observed after photoprocessing, Alternatively, the mercury compound may change the surface charge to permit easier penetration of developers through the lattice. Regardless of any theoretical explanation, the fact remains that the arylmercuric compounds do provide excellent results which are not attainable with the ordinary photosensitive materials alone. For example, with ordinary graphic arts silver halide film, the usual gamma value is from about 4 to about 6, whereas with the arylmercury compound, the

gamma values observed thus far are usually about 12 and 'higher. -In general, the processed media of this invention are characterized by maximum density in the image areas and, for practical purposes, almost zero density in the non-image areas. This is especially desirable in photographically producing printing plates in that maximum density is obtainable with very few gray steps, usually only 1 or 2 gray steps being encountered;

The arylmercury compounds broadly contemplated are those in which the mercury atom is directly bonded to an aromatic ring structure, i.e. a cyclic structure stabilized by resonance, classically illustrated by the henzene ring. Such compounds include, for example, phenyl mercurials such as phenylmercuric acetate, phenylmercuric chloride; phenylmercuric bromide, and the like. Of course, the phenyl group can be replaced by analogous aryl groups derived from naphthalene,,anthracene' and phenanthrene, as well as heterocyclic compounds such as thiophene, furan, indole, thiazole, thiadiazole, pyridine, and the like, as well as fused ring systems such as benzothiophene and benzofuran. The presence of substituents on the aromatic nucleus is not critical when such substituents do not adversely affect the photographic properties of the photosensitive emulsion, either ,in;-the photoexposure or in the photoprocessing, i.e. such substituents should be photographically acceptable. In addition, the arylmercuric compound should not add undesirable color to the photosensitive emulsion. Consequently, unsubstituted arylmercuric compounds are usually preferred.

DESCRIPTION OF PREFERRED EMBODIMENTS The preferred arylmercuric compounds are those corresponding to the formula:

in which Ar is a monovalent, aromatic nucleus and X is a monovalent negative ion. The preferred aromatic nucleus is phenyl or substituted phenyl, in which the substituents are halogen, lower alkoxy or lower acyloxy. The extent of substitution of such groups on the aromatic nucleus is not critical, so that the nucleus can be mono-, di-, or even trisubstituted without altering the effectiveness of the compound in the present invention. Of course, the substituents on the aromatic nucleus should preferably not give rise to adverse color in the photographic layer and, further, should preferably not react adversely under the conditions of photoprocessing, i.e. the substitutents should be photographically acceptable. Such preference also exists with regard to the monovalent negative ion X and the aromatic nucleus each of which should also be photographically acceptable.

The substituent, X, can be any suitable negative ion but preferably is an acryloxy group, especially the lower alkanoyloxy, e.g. acetate, propionate, caproate. Other negative ions which can be used are halide, such as chloride or bromide, nitrate and the like.

The preferred arylmercuric compounds are those which are readily-dispersible in the photosensitive layer and, of course, are photographically compatible with the photosensitive material. At present, the particularly preferred compounds are the phenyl-mercuric alkanoates, and of these phenylmercuric acetate which is readily available and at the same time economical. For particular photographic results or special effects, a minimum of experimentation by those skilled in the art will permit the selection of appropriate arylmercuric compounds, which selection, of course, will depend, in great part, on the type of photosensitive system utilized.

The preferred photosensitive media are those comprising silver halide as the photosensitive material. Such photosensitive media. are more than adequately described in the literature and are well-known to those in the art. Especially preferred silver halide media are those which contain a low content of silver, as silver halide, in the photosensitive layer, particularly media comprising thin photosensitive layers as described in the aforesaid copending application.

'In a preferred form of the invention, the arylmercuric compound is added to an emulsion of the photosensitive material in a binder before the emulsion is coated on a support to form the photographic medium. In this way, uniform distribution of the arylmercuric compound throughout the photosensitive layer is insured. For such purpose, the arylmercuric compound is dissolved in a solvent compatible with the emulsion, e.g. usually a lower alkanol such as methanol, ethanol or propanol, and merely added to the emulsion at any convenient point in the preparation of the emulsion. For example, when the silver halide, e.g. chloride, is prepared in the emulsion by mixture of silver nitrate and a soluble halide, e.g. chloride, it is usually convenient to add the arylmercuric compound after'silver halide formation and then mix thoroughly to obtain'uniform distribution'of both materials in the emulsion. As an alternative the arylmercuric compound can be added to'the emulsion system prior to formation of the "silver halide. Although not-preferred, the arylmercuric compound can be added to the photosensitive layer after it has been formed on the medium, e.g. by merely immersing'the photographic'medium in'a solution of the selected compound and allowing the layer to absorb by imbibing. Results obtained with media so produced are not of the high order obtained with media produced by the preferred preparative method.

The amount of arylmercuric compound used in the present invention can be varied over wide ranges depending on the desired results and the photosensitive materials employed. A minimum amount of experimentation will permit the selection of optimum concentrations by the mere expedience of preparing media at various concentrations of the arylmercuric compound and selecting the optimum concentration determined. For photographic purpose, it is. preferable to select almost minimum effective concentrations of any materials to be added to a photosensitive layer. Since mercuric compounds are known for their toxicity, it is also desirable to the amount of the arylmer'curic compound in the photosensitive layer.

For most purposes, it has been found that a concentration of from about 1% to about 7.5% by weight based on the photosensitive material meets such criteria but of course the use of more or less than the said amount will not materially affect the desired results. Generally, from 0.5% up to about 15% by weight will be the most practical range. Usually, the arylmercuric compound at con- 7 centrations higher than about 15% causes a noticeable reduction in photographic speed and such high concentrations are thus undesirable in that effect.

The invention contemplates the provision of new photographic media which are characterized by comprising a photosensitive material together with an arylmercuric compound in the photosensitive layer. The arylmercuric compound is preferably uniformly distributed with the photosensitive material in a photosensitive layer on a suitable substrate therefor. The photographic media can beany of those commonly used and known to those skilled in the art. The photosensitive material and the arylmercuric compound are suitably contained in a layer of binding material, such as gelatin, polyvinyl alcohol, polyacrylates and polymethacrylates, as well as copolyrners of acrylates and methacrylates. Many such binders vare well known in the art and are intended for use in the new media of this invention. I

The substrates for the present media include all of the substrates commonly employed such as paper, plastics and metal substrates. For example, cellulose acetate and poly- '4 a ethylene terephthalate can be used for transparent films while metals, such as aluminum and iron, as well as alloys thereof, can be used and are particularly adapted for photographically producing printing plates and printed electrical components, e.g. printed electrical circuits, capacitors, and the like, as well as nameplates and decorative metal plates.

The preferred new photographicmedia are' those in which silver halide is the photosensitive material. Especially preferred are the low silver-content, 'thinphotosensitive layer media described hereinbefore. These media are characterized by a photosensitive-layer thickness of less than one micron and preferably less than aboutBOO millimicrons. Most preferred layer thickness is less than about 1-00 millimicrons. The silver content of such layers is usually about .05 gL/m. and may be" as low as 0.01 g./m. in the most preferred layer thickness, as, described in, the aforesaid copending application. 7 v

The photosensitive material can also be any of the photosensitive photoconductors, such as described in the patent literature, for example, British specification 1,043, 250, incorporated herein by reference. Generally, the pre ferred photoconductors are compounds of a metal with a non-metallic element of Periodic Group VI. Preferably, these photoconductors are metal oxides or sulfides, such as titanium dioxide, zincoxide, zinc sulfide, cadmium sulfide, and cerium oxide, among-others. Preferred are titanium dioxide, zinc oxide and mixtures thereof.

The photosensitive material and the aryl'mercuric'compound in the selected binder are applied to the substrate using any of the art-recognized techniques, by use of rollers, in the desired thickness. After drying the photographic media are ready for use. If desired a top coating can be applied to protect the photographic emulsion; Of course, the emulsion can also contain substances coin monly employed with the specific photosensitive material, such as dyc-sensitizers, sensitizing-metal salts, such'as silver and copper salts, photographic reducing agents, and such materials commonly used in photographic emulsions.

The photoexposure step employed is the same as nor mally used for the selectedphotosensitive material! The photoprocessing of the exposed medium is also'thefsam'e as normally employed, the exception in the photoprocess ing being a much shorter induction period inimageformation which is one of the characteristics of the present new media.

A particularly preferred embodiment of the p esent invention is the provision of especially eifective photographic media for the production of printing plates and electrical components. Especially desirable properties; of high density in image areas and little, if any, density in non-image areas makes the new media of the present invention extremely well-suited for the said uses. 01: the present new media those which are characterized by a metal substrate are particularly well-suited for printing plate production, especially utilizing the lowcontent .silver, thin photosensitive layers hereinbefore described. These thin layer low silver content metal photographic media can be processed to printing plates of which the photographically produced metal image is 'adhercntly bonded to the metal substrate. After treatmentof the produced metal image to render same receptive of ink, the plates are very durable and can be used in the printing of hundreds of thousands of cor')ies,an"d often more than almillion copies without'plate failure due to separation of the image metal from the substrate metal. i I Q For metal plates of the type described, aluminum sub} strates are preferred especially anodized aluminum. The surface in contact with the photosensitive emulsionis preferably a roughened surface, as by chemicalroughening or physical roughening. The latter is preferred and is conveniently accomplished by brush-grainingthe surface, especially using nylon brushes to attain the desired roughening. I

The so-called low silver content, thin photosensitive layer constitutes a preferred form of the invention, particularly with metal substrates for the production of printing plates, electrical components, and the like. -As described in the aforesaid copending application, the silver halide employed is that which is conventionally used in photography and is made in the conventional way, i.e. by reaction in aqueous systems of soluble silver salt such as silver nitrate or sulfate and a soluble alkali metal halide, such as sodium chloride, sodium bromide or sodium iodide, or corresponding potassium salts. The formation of the particles of silver halide can be controlled to permit any desired particle size, ranging from as little as 30 to 50 angstrom units up to conventional particle size. Preferred methods are those which encourage fine particle size, usually less than 0.5 micron. For general convenience, such fine particle size is obtained by using systems of high solids content, preferably at approximately total solids (including the Weight of silver halide and the binding agent) and rapidly mixing the soluble alkali metal halide solution with the soluble silver salt solution, usually at about room temperature, for convenience.

The binder employed can be any of those conventionally used in forming silver halide emulsions. Preferably, the binder should be wettable by aqueous solutions to a sufiicient degree to permit rapid processing of the exposed layer. Preferred binders are the usual gelatin, so common in silver halide films, polyvinyl alcohol, polyacrylates, including polyacrylic acids, casein and the like. The use of polyvinyl alcohol is especially preferred where fine particle size of the silver halide is desired since the binder apparently discourages ripening, i.e. growth of the silver halide particles which occurs on standing.

The binder, of course, is added to the aqueous system used to form the silver halide particles, as a matter of convenience. In addition, other materials can be added to the binder-aqueous system as desired to obtain specific effects in the photosensitive layer during or after expo sure. For example, sensitizing dyes, thiourea, toners, mercurie salts or the like can be added for their known photographic effects, e.g. thiourea to assist in formation of black photographic images, and the sensitizing dyes to alter the spectral response of the layer on photoexposure.

After addition of the arylmercuric compound, the emulsion is then coated on a substrate. The coating process can be any of those commonly employed, e.g. air knife, roller coating or similar such coating means. With proper settings, a coating weight of about 0.5 gram per square meter can be readily attained and gives a uniform layer of about 0.5 micron. By adjustment, thinner layers, e.g. 0.2-0.3 micron and even lower, can be made. Thicker layers up to one micron and higher present no problem to those skilled in the art. The optimum layers are produced with a ratio of silver halide to binder of from about 3/1 to about l/3.

The preferred thin layers, i.e. of thickness below one micron, usually contain as silver halide, approximately 0.3 gram of silver per square meter.

The development of visible images when using the described thin photosensitive layers is preferably accomplished by physical development, which may include, as an initial step, the usual chemical development used in silver halide photography, e. g. hydroquinone aqueous solution at alkaline pH values.

The physical developers which are preferred are socalled stabilized physical developers, particularly those which are most effective at acid pH value, i.e. below pH 7. Especially preferred are the so-called mono-bath physical developers which are stabilized. Monobath physical developers consist of a single solution of reducible metal ion and the reducing agent therefor. On prolonged use, there 'is apparently a tendency to the formation of undesired side products. Stabilized monobath physical developers are known in the art and usually include surfactants or similar such materials which prolong the life of the physical developer. One of the basic problems with physical developers is the tendency toward decomposition with formation of insoluble materials that contaminate photographic emulsions or otherwise are undesirable in terms of their adverse effect on the acceptability and/ or aesthetics of the photographic image. The surfactants apparently minimize such decomposition, i.e. stabilize the physical developer.

The optimum results attainable with the physical developers is at pH values below 7, i.e. in acid media, usually at about pH 1.5. Lower pH values should be avoided because of the possible adverse effect on the surfactants which are sensitive to low pH values.

In the physical developers employed, the reducible metal ion is usually of a metal at least as noble as copper, e.g. silver, copper, gold, platinum, palladium and the like. However, other metal ions such as nickel and tin can also be used, with appropriate reducing agents. Reducing agents for copper, silver and like noble metal ions are readily determinable and are fully described in the literature.

A particularly effective monobath physical developer is composed of silver ion and, as reducing agent therefor, the ferrous-ferric ions developer which is well-known to the art.

For best results, the monobath physical developers are usually prepared immediately before use to increase the useful life of the system. The surfactants are added during formation of the monobath to obtain maximum stabilization.

The physical developers may contain additional materials which assist in formation of the desired type of photographic image. Thus, for example, complexing agents for the metal ion to be reduced may be present, or toners which aifect the physical appearance of the resulting photographic image.

In lieu of the described monobath physical developers, there may be used separate solutions of the reducible metal ion and the selected reducing agent. For example, the physical developer can be made up of separate solutions of silver ions, and Metol. The exposed layer is first immersed in the silver ion solution and subsequently in the Metol solution. The results obtained are quite acceptable but the separate steps are undesirable for obvious reasons of time and labor waste. Additionally, the results are not always as reliable with reference to the reproducibility, desirable photographic image characteristics as those attainable with monobath physical developers, especially in stabilized form.

The physical developer, irrespective of monobath, separate solutions or stabilization, can be applied to the photosensitive layers in the form of viscous solutions or gels with essentially the same results as the liquid systems. The efliciency of viscous solutions, and particularly gels, make these forms of the physical developer particularly desirable in commercial use of the present new thin photosensitive layers.

When preparing printing plates from the new media of the present invention, physical development is continued until the photographic image is adherently bonded to the substrate, e.g. aluminum substrate. After producing the adherently bonded metal images, the media can be treated to produce a printing plate, e.g. by removal of the photosensitive layer binder, lacquering of the metal image or chemically treating the metal image to render it receptive of ink. The treatment of the metal image to obtain a printing plate is by art-recognized procedures.

Alternatively, when electrical components or nameplates are the desired products, the final treatment thereof is also by art-recognized procedures. For example, nameplates can be lacquered, with or without color to attain any desired aesthetic effect.

The photosensitive media of the present invention can be further modified by incorporating therein other materials which affect the photosensitive materials, e.g. sen- 7 sitizing dyes, and other such materials which are commonly employed with the photosensitive material. For example, the reducing agent of the image-forming system employed can be present, as well as the metal ion of the physical developer, or alternatively, the entire physical developer system, all of which can be incorporated into the photosensitive layer or in separate layers on the substrate as is knownin the art.

EXAMPLE 1 A solution of polyvinyl alcohol (PVOH) is prepared by slowly adding the resin powder to distilled water at room temperature with rapid stirring. The temperature is slowly raised to 95 C. while maintaining rapid agitation, and held at,95 C. for about 0.5 hour.

The following solutions are prepared using the 5% PVOH solution thus prepared:

(Solution B is not prepared until immediately before the described use, i.e. freshly prepared before mixing with Solution A.)

Solution A is added to Solution B under good agitation within about 5 seconds total addition time, at room temperature. The mixture is then sonified (Bronson Sonifier) for 4 minutes at about 100 watts. Then, 248 parts of 5% PVOH solution is added to the mixture under good agitation. Phenylmercuric acetate in methanol is then added at 3.0% by weight based on silver chloride and the agitation is continued for about 5 minutes thereafter. Subsequently, the mixture is filtered through a five micron bag to obtain an emulsion of the following :characteristics:

Emulsion constants 1:2 rates of silver chloride to PVOH excess chloride 4.5% total solids 12.4 g. silver chloride/liter pH=5.9 to 6.2 Viscosity=6 to 8 cps.

The emulsion can then be coated on a substrate by A lustrous, coherent, metallic image is obtained on the film. Similar results are obtained with silver chlorobromide (80:20) film. I

The solutions are mixed in the following order: Solution A is added to Solution B, Solution C is added to the mixture. The mixture is stirred and filtered as in Example 1, toobtain an emulsion of the following characteristics:

Emulsion constants i 1.3 silver chloride to hinder either air knife, roller coating or similar coating means.

Good results are obtained using a roller coater with hard rubber rolls. With proper settings, a coating weight of .05 g./m. can readily be obtained.

A polyester film having a single vinylidene chloride copolymer subbing layer is so coated and thoroughly dried by heating at about 27 C. for ten minutes. The coated film is then exposed and developed in the following stabilized physical developer:

6.0 Brlng t0 1 liter with distilled water.

10% excess chloride 4.5 total solids 9.7 grams silver chloride per liter 1% mercury on binder solids pH=7.7 to-8.0

Viscosity=6 to 8 cps.

The combined solutions are used to coat a subbed, polycoated paper stock with a roller coater and the paper then is exposed and developed as in Example 1. The silver chloride particle size (average), ranges from 50 to 200 'A. and the layer thickeness is about 0.1 micron.

EXAMPLE 3 An emulsion containing 8% excess silver at a total solids. content of 4.4% is prepared from the following solutions:

. Solution I 1800. 3 N AgNO 210 cc. H O H I 72 g'rns. Lemol 16-98 (10%) Solution II 3 gms. NaCl 72 gms. Lemol 16-98 Solution II is added to Solutioin I rapidly with stirring, phenylmercuric acetate in methanol is then added at 4.5 by weight based on silver chloride, and the mixture is then sonified for 5 minutes. The emulsion isthen-used to coat any desired substrate-film, paper, aluminum metal-at .a coating weight of about 0.5 g./m. i.e. at a thickness of one micron orless.

- The coated substrate isthen exposed and processed as in Example 1.

Formaldehyde (3%) gm 1 7, Solution A is poured into Solution B at 60 C., phenylmercuric acetate in methanolis then added at 3.0% by weight based on silver chloride, and the resulting mixture vigorously stirred for 3 minutes. After cooling to 30 C., the mixture is coagulated by rapid addition of methanol and distilled water 1:1 cooled to 12 C. The mixture is stirred until coagulum forms and the liquid clears. The coagulum is removed and cut'into small noodles which are washed twice with cold distilled water. The coagulum is then dissolved in water to form one liter aqueous emulsion which is then used to coat substrates as in the previous examples.

EXAMPLE f The procedure of Example 1 is repeated substituting ametal substrate for the paper substrate and utilizing the following physical developers: 1

AgNO 3M 7 mi 15 Metol g Citric acid g 80 Water to 1 liter.

and then, in a physical developer solution is 0.5 CuEDTA and 0.5 M Na EDTA. The resulting copper amplified image is adherently bonded to the substrate.

EXAMPLE 6 The procedure of Example 1 is repeated with the added step of chemical development by immersion in a standard developer, e.g. Kodak D-19 or D-76, prior to physical development, and the resulting image is of greater detail than that obtained in Example 1.

EXAMPLE 7 The procedure of Example 6 is repeated with the exceptionthat the physical developer is the following solution: I

CuSO (1 M) Triethanolamine. (0.75 M) 50 Ascorbic acid'(l M) 50 Comparable-results are obtained.

' j EXAMPLE 8 I The procedure of Example 1 is repeated with the exception that the physical developer is the following solution:

' The procedure of Example 1 isrepeated to form a printed electrical circuit consisting of silver.

The printed circuit is then amplified to an additional thickness of 1-5 mils by electrolytic deposition of copper using a conventional'copperizing bath, e.g. CuSO /H SO solution at coating electrical current.

The metal printed circuit is adherently bonded to the substrate.

I EXAMPLE 10' The procedure of Example 2 is repeated using a brushgrained anodized aluminum sheet as substrate in lieu of paper.

. The resulting plate is then wiped with a dispersion of mercaptobenzothiazole (e.g.) phosphoric acid (5 ml. 85%) and dodecylammonium chloride (0.5 g.) in one liter of water. The silver image will now accept lacquer or ink depending on Whether it is to be used as a color image (by inclusion of color in the lacquer) or as a printing plate.

The metal image is adherently bonded to the aluminum substrate. EXAMPLE 11 In a reaction flask equipped with a stirrer, a nitrogen inlet, a dropping funnel, and a condenser are placed 10 liters of water and 2.88 liters of a 10% aqueous solution of the sodium salt of sulphonated dodecyl benzene. Then the reaction flask is rinsed with nitrogen and the liquid is heated to 60 C. In another flask are placed successively 800 cc. of isopropanol, 144 g. of N-vinylpyrrolidone, 108 g. of n-butyl acrylate, 830 g. of N-tert.- butylacrylamide and 2520 g. of vinylidene chloride. The mixture is stirred and brought to dissolution by gentle heating. 8

Through the dropping funnel a-solution is added of 21.6 g. of ammonium persulphate in 400 cc. of water. Immediately pumping of the monomer solution into the reaction flask is started. The rate of pumping is such that after 75 all the monomer solution is pumped over. Together with the monomer solution a further amount of ammonium persulphate solution is added dropwise (64.8 g. in 1200 cc. of Water). During the whole reaction period the temperature of the mixture is maintained at 60 C. while refiuxing.sAfter all the monomer has been added, again an amount of 21.6 g. of ammonium persulphate dissolved in 400 cc..of Water is addedat once After refluxing, stirring is continued for another 30 min. at 60 C., whereupon the reaction mixture is cooled to room temperature.

In order to precipitate the copolymer of vinylidene chloride, N-tert.-butylacrylamide, n-butyl acrylate, and N-vinyl-pyrrolidone (70:23:324), the latex formed is poured into a mixture of 40 liters of 10% aqueous sodium chloride solution and 40 liters of methanol while stirring. The fine grainy precipitate which is obtained is repeatedly washed with water and finally dried.

An amount of 2.5 g. of the vinylidene chloride copoly mer formed above are dissolved in a mixture of cc. of butanone and 10 cc. of nitroethane. The solution obtained is warmed to 25 C. and coated on a plate of polymethyl methacrylate in such a way that 0.75 to 1.0 g. of copolymer is present per sq. m. This layer is dried at room temperature.

A copolymer latex is prepared as follows:

In a 20-liter autoclave are placed successively- Water boiled under nitrogen liters 10.2 10% aqueous solution of oleylmethyltauride do 0.6 10% aqueous solution of the sodium salt of heptadecyl-disulphobenzimidazole do 0.6 Azodiisobutyronitrile g 6 Butadiene a 1500 Methyl methacrylate g 1500 After sealing of the autoclave, the strongly stirred emulsion is polymerized for 6 hr. at 60 C. This polymerization is slightly exothermic for a short while. Then the pressure drops rapidly. The polymerization is finished under reduced pressure. The latex of the copolymer of butadiene and methyl methacrylate (50:50) is then freed from residualtraces of monomer by blowing at 60 C. and under a slight vacuum an air current above the latex. Then the latex is cooled and filtered.

The above latex copolymer is now used to prepare an Solution A is added to Solution B with good agitation overa timeperiod of=approximately to seconds. Phenylmercuric acetate in methanol (4% by weight based on silver chloride) is g'DCXt added. Then, 248 parts of a 5% latex copolymenprepared above is added to the mixture under good agitation. The agitation is continued for 30 minutes. The emulsion is then filtered and is ready for coating. The coating may be applied by an air knife, roller coating or other means. The coat weight should be kept at approximately .05 gram' per square meter or below. v a

The subbed polyester film having a single vinyl copoly mer subbing layer is so' coated and thoroughly dried. The coat of the film is then exposed and developed as described in Example 1.

EXAMPLE 12 An emulsion is prepared as described above in Example 11 except that the latex emulsion polymer used is either -AC-22 or AC-33 as obtained from Rohm. 8; Haas. The emulsion is coated to an identical coat weight and manner as inExample 11 and is exposed and processed as described in Example 1.

EXAMPLE 13 The following dispersion is prepared:

Gms. TiO, aq. slurry) 1600 Gelatin (10% aqueous solution) 2000 Methylanethacrylate copolymer (Hydrosol-Du -Pont) (30% dispersion) 670 H O 2500 Humectant (50% aqueous solution) 12 Wetting agent (5% aqueous solution) 70 Hardener 5 Phenylmercuric acetate MeOH) (30% aqueous solution) 60 and then coated on brush-grained, anodized aluminum plates, a dry coating of 0.5 g./m.

Exposure and development is effected as in Example 1 to obtain an adherent metal image which is connected to a long-run printing plate.

Similar results are obtained using diazosulfonates as the photosensitive material on aluminum plates for example, as described in U.S Pat. 3,390,988.

14 This example illustrates a typical "contrast silver chloride medium. The following solutions are prepared:

' H,O250 mls.

NaCl'7.5 gms. CdCl,.075 gm. KBr-3.5 gms. Gelatin12.5 gms.

I Lo-37s mls. AgNO 20 gms.

Sol. C:

Gelatin-46 gms.

(Note-Selection of high restrained gelatin is most important for obtaining high gamma.)


12 EXAMPLE 15 i This example illustrates a comtmodsilver-bromoiodide medium. The following solutions are prep'aretd: Sol. A: i H O1500 gms.

KBr-l4'6 gms. r KI-4.4 gms. I g ..Gelatin57.5 gms. r I t Sol. Bi-

' gins. AgNO --176 gms.

Sol. C: 11 0-250 mls.

- .Gelatin222 gms. l a v Solution B was percolated into Solution A in'45 seconds at 160 F. and ripened for30 l'i'iinutes atl 60 F.,then cooled to 110 F. where Solution C was added and held mixing for 20 minutes. The emulsion was then cooled to set, refrigerated 16 hours, noodled, washed and remelted ,to 115 F. where '100 gms. gelatin was adjusted inyolume to 5,500 grams and to pH of 6.54. The above formulation is made up to 20 gms. Ag perj lite'r of emulsion, to which is added 0.2 g./l. phenylmercuric acetateLfIhe emulsion is then coated, exposed and developed as in' Example 1.

The image contrast the foregoing examples is significantly improved over oth; erwise identical media lacking the phenyln ierciiric acetate; Inspection of the developed media shows that harder or, crisper halftones are obtained. The presenceof the phenylmercuric acetate retards bridging of'halftones which has heretofore been a distinct, problem, especially in Graphic Arts.

What is claimed is: j v I, 4 1. In a photographic medium comprising a photosensi tive material which upon exposure produces a physically developable image, the improvement of having intimately associated with the photosensitive materialanarylmer curic compound having the formula Ai'HgX wherein Ar represents an ar'yl group and X representsone member selected from the group consisting of' an acyloxy=grolup, a halide group and a nitrate group, said arylmercuric compound being present in an amount eifective in increasing the gamma of the final print produced byexposurejand contact of said medium with a stabilized physicaledevele oper comprising a solution of silver ions.

v 2. Medium as in claim 1 wherein the photosensitive material is silver halide. 3. Medium as'in claim 2 wherein thesilver halide silver chloride. 4. Medium as in claim-1 wherein the arylmercuri'c compound is a phenylmercuric loweralkanoate;

5. Medium as in claim 1 wherein the arylmercuric compound is phenylmercuricacetate present in a concentration of from about 0.5% up to about 15% byweight of the photosensitive material present; I 7 6. Medium as in claim 1 wherein the arylmercuric compound is phenylmercuric halide. E

*7. Medium as in claim fi wherein halide is phenylmercuric. chloride. p .8. Medium as in claim 1 whereinthe photosensitive-ma- .the I phenylmiercur ic te rial is a photoconductor.

9. Medium as in claim 8 wherein the photoconductor is a compound comprising a metal and a non-metallic element of. PeriodicaGroup a -11 H '-'-'10.:Medium':as in claim 9whereinithe photoconductor is a metal oxide or metal sulfide. g Y 11. Mediumas in claim-'10 wherein the photocondu c'tor is titanium dioxide'or'zinjc oxide ormixtures thereof. .12. In a photographic mediumcomprising a photo sensitive layer. comprising-silver halide in a binder there for,- the improvement comprising an arylrnercuric-=compound in the photosensitive layer, said ar'ylmercuric comand image tone of theproducts of pound having the formula ArHgX wherein Ar represents an aryl group and X represents one member selected from the group consisting of an acyloxy group, a halide group and a nitrate group and said arylmercuric compound being present in an amount efiective in increasing the gamma of the final print produced by exposure and contact of said medium with a stabilized physical developer comprising a solution of silver ions.

13. Medium as in claim 12 wherein the thickness of the photosensitive layer is less than about 300 millimicrons.

14. Medium as in claim 13 wherein the silver content of the photosensitive layer is up to about 0.6 g./m.

15. Medium as in claim 12 wherein the thickness of the photosensitive layer is less than about 100 millimicrons and the silver content thereof is about 0.05 g./m.

16. Medium as in claim 12 wherein the arylmercuric compound is phenylmercuric acetate present in a concentration of from about 0.5% up to about 15% by weight of the photosensitive material present.

17. Medium as in claim 12 wherein the phenylmercuric halide is phenylmercuric chloride.

18. A photosensitive medium comprising on a metal substrate a photosensitive layer comprising silver halide and phenylmercuric acetate in a binder therefor, the thickness of said layer being less than about 300 millimicrons.

19. Medium as in claim 18 wherein the silver content of said layer is up to about 0.5 g./m.

20. Medium as in claim 18 wherein the thickness of said layer is less than about 100 millimicrons.

21. Medium as in claim 18 wherein the metal substrate comprises aluminum.

22. Medium as in claim 21 wherein the aluminum is anodized.

23. Medium as in claim 21 wherein the aluminum is anodized and the surface in contact with the photographic emulsion is a roughened surface.

24. Medium as in claim 22 wherein the surface in contact with the photographic emulsion is a brush-grained surface.

25. In a photographic medium comprising a photosensitive photoconductor layer on a support therefor, the improvement which comprises an arylmercuric compound in the photosensitive layer, said arylmercuric compound having the formula Ar'HgX wherein Ar represents an aryl group and X represents one member selected from the group consisting of an acyloxy group, a halide group and a nitrate group said arylmercuric compound being present in an amount elfective in increasing the gamma of the final print produced by exposure and contact of said medium with a stabilized physical developer comprising a solution of silver ions.

US. Cl. X.R. 96-107, 108

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3862843 *Jun 1, 1972Jan 28, 1975Itek CorpPhotographic element containing a layer of physical development nuclei less than two microns in thickness and a development activator
US3973967 *Aug 19, 1974Aug 10, 1976Itek CorporationProcesses utilizing photographic element containing a physical development activator
U.S. Classification430/496, 430/413, 430/599, 430/416, 430/414, 430/417, 430/526, 430/564
International ClassificationG03C1/496, G03C1/494
Cooperative ClassificationG03C1/496
European ClassificationG03C1/496
Legal Events
Nov 20, 1990ASAssignment
Effective date: 19890711