Copolymeric mordants and photographic products and processes containing same

REFERENCE TO RELATED APPLICATION
The present application is related to the copending patent application of J. Michael Grasshoff, et al. for VINYLBENZYL THYMINE MONOMERS AND POLYMERS AND PRODUCTS PREPARED FOR THE SAME, Ser. No. 08/242,253, filed of even date, which copending patent application discloses and claims certain vinylbenzyl (and vinylphenyl) thymine compounds and polymers, thereof useful in the production of image-receiving elements and other photographic products of the present invention.
BACKGROUND OF THE INVENTION
This invention relates to copolymeric materials having dye mordanting capability. More particularly, it relates to copolymeric mordant materials especially suited to application in photographic diffusion transfer products and processes.
Diffusion transfer photographic products and processes have been described in numerous patents, including, for example, U.S. Pat. Nos. 2,983,606; 3,345,163; 3,362,819; 3,594,164; and 3,594,165. In general, diffusion transfer photographic products and processes involve film units having a photosensitive system including at least one silver halide layer usually integrated with an image-providing material, e.g., an image dye-providing material. After photoexposure, the photosensitive system is developed, generally uniformly distributing an aqueous alkaline processing composition over the photoexposed element, to establish an imagewise distribution of a diffusible image-providing material. The image-providing material is selectively transferred, at least in part, by diffusion to an image-receiving layer or element positioned in a superposed relationship with the developed photosensitive element and capable of mordanting or otherwise fixing the image-providing material. The image-receiving layer retains the transferred image for viewing and in some diffusion transfer products, the image is viewed in the layer after separation from the photosensitive element, while in other products, such separation is not required.
Various polymeric materials have been utilized as mordants in photographic products and processes including those of the diffusion transfer type. Thus, polymeric mordants suited to application in diffusion transfer products and processes for the formation of photographic images in dye are described, for example, in U.S. Pat. Nos. 3,148,061 (issued Sep. 8, 1964 to H. C. Haas); 3,758,445 (issued Sep. 11, 1973 to H. L. Cohen, et al. ); 3,770,439 (issued Nov. 6, 1973 to L. D. Taylor); 3,898,088 (issued Aug. 5, 1975 to H. L. Cohen, et al.); 4,080,346 (issued Mar. 31, 1978 to S .F. Bedell); 4,308,335 (issued Dec. 29, 1981 to T. Yamamoto, et al.); 4,322,489 (issued Mar. 30, 1982 to E. H. Land, et al.); 4,563,411 (issued Jan. 7, 1986 to I. Y. Bronstein-Bonte); and 4,794,067 (issued Dec. 27, 1988 to Grasshoff et al.).
The utilization of a particular mordanting material in a photographic product or process will oftentimes depend upon the particular requirements of a photographic product or process and deficiencies or disadvantages associated with the use of a particular mordanting material may be observed. Deficiencies in mordanting capacity, particularly, with respect to one or more dye material desirably utilized, may be noted. Accordingly, the provision of mordanting materials which exhibit favorable maximum density (Dmax) values, is particularly desirable insofar as such properties permit the attainment of desired image formation and quality of photographic reproduction. Desirable mordanting benefits may be realized in some instances by utilizing copolymeric mordant materials obtained, for example, by the polymerization of a polymerizable mordanting compound along with one or more copolymerizable compounds. Examples of copolymeric mordants are disclosed, for example, in the aforementioned U.S. Pat. Nos. 3,770,439; 3,898,088; 4,308,335; 4,322,489; 4,563,411 and 4,794,067. The suitability of a copolymeric mordant will be dictated largely by;the particular monomeric compounds used in the preparation thereof and the particular nature of a photographic system. In addition, difficulties in the synthesis of such copolymeric mordanting materials, and in the production of efficient mordanting materials that can be readily coated into a suitable image-receiving layer, may present formidable limitations upon practical utilization.
It is an object of the present invention to provide polymeric mordant exhibiting efficient dye mordanting capability.
It is another object of the present invention to provide polymeric mordants exhibiting such mordanting capability and adapted to utilization in photographic products and processes.
Still another object of the present invention is the provision of polymeric mordants capable of ready synthesis and efficient utilization in the preparation of coated image-receiving layers containing such polymeric mordants. Other objects of the present invention will become apparent from the description appearing hereinafter.
SUMMARY OF THE INVENTION
There is provided by the present invention a class of efficient mordanting polymers especially adapted to utilization in photographic products and processes of the diffusion transfer type. These polymeric mordants are copolymeric mordant materials containing recurring units according to the formula ##STR2## wherein each of R.sup.1, R.sup.2 and R.sup.3 is independently alkyl (e.g., methyl, ethyl, propyl, butyl); substituted-alkyl (e.g., hydroxyethyl, hydroxypropyl); cycloalkyl (e.g., cyclohexyl); aryl (e.g., phenyl, naphthyl); aralkyl (e.g., benzyl); alkaryl (e.g., tolyl); or at least two of R.sup.1, R.sup.2 and R.sup.3 together with the quaternary nitrogen atom to which they are bonded complete a saturated or unsaturated, substituted or unsubstituted nitrogen-containing heterocyclic ring (e.g., morpholino, piperidino or 1-pyridyl); X is a counteranion (e.g., halide); each of R.sup.4 and R.sup.5 is hydrogen or alkyl (e.g., methyl); Z is hydrogen or methyl; n is an integer 1 or 2; and wherein each of a and b is the molar proportion of each of the respective repeating units. From inspection of Formula I, it will be appreciated that the copolymeric mordants contain recurring units from a thymine derivative (where R.sup.4 is methyl) or from a uracil derivative (where R.sup.4 is hydrogen). For convenience, such recurring units are referred to collectively as recurring units from a thymine or uracil monomeric derivative.
Examples of thymine and uracil derivatives useful for preparing copolymeric mordants of the invention include 1-(vinylbenzyl) uracil (VBU); 1-(vinylbenzyl)-3-methylthymine (VBMT); 1-(vinylphenyl) thymine (VPT), i.e., the compound where n is the integer one; and a preferred monomer, 1-(vinylbenzyl) thymine (VBT).
As used herein, and except as otherwise noted, the recitation "VBT" is sometimes used to refer to a class of the aforedescribed vinylbenzyl (and vinylphenyl) thymine and uracil derivatives, and also, to the specific compound, 1-vinylbenzyl thymine.
It has been found that copolymeric materials comprising recurring units from a vinylbenzyl quaternary ammonium salt and a thymine or uracil monomeric derivative, each as aforedescribed, exhibit efficient mordanting capacity and are especially suited as mordants in photographic products and processes.
In a product or article aspect of the present invention, there is provided an image-receiving layer comprising a copolymeric mordant as aforedescribed. In another of its product or article aspects, the present invention provides a diffusion transfer film unit which comprises a photosensitive system comprising at least one photosensitive silver halide emulsion layer having associated therewith a diffusion transfer process image dye-providing material and an image-receiving layer adapted to receive an image dye-providing material after photoexposure and processing, the image-receiving layer comprising a copolymeric mordant as aforedescribed.
In a process aspect of the present invention, there is provided a process for forming a diffusion transfer image which comprises the steps of exposing a photosensitive system comprising at least one photosensitive silver halide emulsion layer having associated therewith a diffusion transfer image dye-providing material; contacting the exposed photosensitive system with an aqueous alkaline processing composition, thereby effecting development of the silver halide emulsion (or emulsions) and the formation of an imagewise distribution of diffusible image dye-providing material; and transferring, by imbibition, at least a portion of the imagewise distribution of diffusible image dye-providing material to a superposed image-receiving layer comprising a copolymeric mordant as aforedescribed.

For a fuller understanding of the nature and objects of the invention, reference should be had to the following detailed description taken in connection with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a diagrammatic cross-sectional view of an image-receiving element of the invention comprising a support material; a polymeric acid-reacting layer, a timing layer, an image-receiving layer of the invention and an overcoat layer. FIGS. 2 to 4 are simplified or schematic views of particular arrangements of film units embodying an image-receiving layer of the present invention and shown after exposure and processing.

DETAILED DESCRIPTION OF THE INVENTION
As mentioned previously, the present invention is directed toward copolymeric mordant materials and to photographic elements, products and processes utilizing such copolymeric mordant materials. When utilized in the image-receiving layers of the photographic elements or products of this invention these copolymeric mordant materials function to fix or mordant diffusible dye image-providing materials. Thus, color images can be formed in image-receiving layers comprising the copolymeric mordants of the present invention by transferring to the image-receiving layer an imagewise distribution of diffusible image dye-providing material and utilizing the copolymeric mordant to fix and hold the transferred dye in the layer.
As can be appreciated from inspection of Formula I, the copolymeric mordants of the present invention comprise recurring units resulting from the polymerization of copolymerizable ethylenically-unsaturated comonomers. Thus, the copolymers comprise repeating or recurring units from a copolymerizable vinylbenzyl quaternary ammonium salt having the formula ##STR3## wherein each of R.sup.1, R.sup.2, R.sup.3 and X have the meanings hereinbefore ascribed.
The nature of the quaternary nitrogen groups of the compounds of Formula II and of the recurring units of the copolymeric mordants of the invention can vary with the nature of the R.sup.1, R.sup.2 and R.sup.3 groups thereof. Thus the R.sup.1, R.sup.2 and R.sup.3 substitutents on the quaternary nitrogen atom of the compounds of Formula II, and present in the recurring units of the copolymeric mordants hereof, can each be alkyl (e.g., methyl, ethyl, propyl, butyl); substituted-alkyl hydroxyethyl, hydroxypropyl); cycloalkyl (e.g., cyclohexyl; aryl (e.g., phenyl, napthyl); aralkyl (e.g., benzyl); or alkaryl (e.g., tolyl). Preferred R.sup.1, R.sup.1 and R.sup.3 groups include alkyl, such as alkyl groups of from 1 to about 8 carbon atoms; cyclohexyl; and benzyl. Especially preferred compounds represented by Formula II and providing recurring units of the copoylmeric mordants hereof are those wherein each of R.sup.1, R.sup.2 and R.sup.3 is the same alkyl group such as methyl. Other preferred compounds herein are those, for example, wherein R.sup.1 and R.sup.2 are each aklyl, e.g., methyl, and R.sup.3 is cyclohexyl.
As indicated previously, the groups R.sup.1, R.sup.2 and R.sup.3 of the compounds of Formula II, and of the corresponding recurring units of the copolymeric mordants hereof, can complete with the quaternary nitrogen atom a nitrogen-containing heterocyclic ring. The nitrogen-containing heterocyclic ring can comprise a saturated or unsaturated ring and, additionally, can be a substituted or unsubstituted heterocyclic ring. It will be appreciated that the formation of a saturated N-containing heterocyclic ring will involve two of the R.sup.1, R.sup.2 and R.sup.3 groups while in the formation of an unsaturated nitrogen-containing heterocyclic ring such as 1-pyridyl, each of groups R.sup.1, R.sup.2 and R.sup.3 will be involved. Other examples of suitable nitrogen-containing heterocyclic groups formed with the quaternary nitrogen atom include morpholino and piperidino.
The particular nature of the R.sup.1, R.sup.2 and R.sup.3 substitutents of the compounds of Formula II and of the copolymeric mordants hereof will depend upon the particular mordanting capability desired in the copolymeric mordant and upon any influence of such substituent groups on such properties of the copolymeric mordants as solubility, swellability or coatability. The R.sup.1, R.sup.2 and R.sup.3 groups of a recurring unit of the copolymeric mordants hereof can, as indicated, be the same or different to suit particular applications. Similarly, copolymeric mordants may comprise recurring units from two or more compounds represented by the structure of Formula II are also contemplated herein. Such copolymeric mordants may comprise recurring units from each of differently substituted compounds exhibiting differences in mordanting capability or affinity to dyes or variously affecting desired properties of the copolymeric mordants. It will be appreciated that copolymeric mordants of this type can be prepared by the polymerization of a thymine or uracil monomeric derivative as aforedescribed with a mixture of two or more dissimilar ethylenically-unsaturated copolymerizable compounds represented by the structure of Formula II, i.e., a mixture of compounds wherein the R.sup.1, R.sup.2 and R.sup.3 substitution of the respective compounds is different.
Suitable mixtures of such dissimilar Formula-II ethylenically unsaturated copolymerizable compounds that can be copolymerized with a Formula-III thymine or uracil derivative to provide a copolymeric mordant useful in the present invention are the mixtures described in the aforementioned U.S. Pat. No. 4,794,067. Especially useful are vinylbenzyl quaternary mixtures which include a compound having a long-chain alkyl group (e.g., vinylbenzyl n-dodecyl dimethyl ammonium chloride) in admixture with a vinylbenzyl quaternary compound having short-chain alkyl groups (e.g., vinylbenzyl trimethyl ammonium chloride, vinylbenzyl triethryl ammonium chloride or a mixture thereof).
The moiety X shown in the compounds represented by structure of Formula II, and in the copolymeric mordants represented by the structure of Formula I, is an anion such as halide (e.g., bromide or chloride). Other anionic moieties representative of anion X include sulfate, alkyl sulfate, alkanesulfonate, arylsulfonate (e.g., p-toluenesulfonate), acetate, phosphate, dialkyl phosphate or the like. A preferred anion is chloride.
Suitable examples of ethylenically-unsaturated monomers representative of compounds of Formula II useful in the preparation of copolymeric mordants of the present invention are vinylbenzyl trimethyl ammonium chloride; vinylbenzyl trihexyl ammonium chloride; vinylbenzyl dimethylcyclohexyl ammonium chloride; vinylbenzyl dimethylbenzyl ammonium chloride; vinylbenzly triethyl ammonium chloride; vinylbenzyl pyridinium chloride. Mixtures comprising positional isomers can be employed. A preferred vinylbenzyl quaternary salt comprises a mixture of positional isomers (para and meta) of vinylbenzyl trimethyl ammonium chloride.
Representative structures of recurring units of the copolymeric mordants of the present invention include: ##STR4##
It can also be appreciated from inspection of Formula I that the copolymeric mordants of the present invention include repeating or recurring units resulting from the polymerization of a thymine or uracil monomeric derivative having the formula: ##STR5## wherein R.sup.4 and R.sup.5 and n have the meanings hereinbefore ascribed. Preferably R.sup.4 will be methyl and n will be an integer 2. A preferred copolymerizable monomeric derivative is 1-(Vinylbenzyl) thymine (VBT) according to the formula: ##STR6## Mixtures of polymerizable monomers from the class represented by Formula III can be employed.
The ratio of recurring units in the copolymeric mordants hereof, represented by integers a and b in the polymers of Formula I, can vary widely. In general, relative proportions will be dependent upon the desired mordanting capacity, contributed largely by the Formula-II vinylbenzyl quaternary ammonium compound, and on the desired physical properties of an image-receiving layer containing the polymer. From inspection of Formula I, it can be seen that the vinylbenzyl thymine and uracil derivatives contain triple hydrogen-bonding sites presented by the cyclic imide group. The H-bonding sites permit non-covalent complexation of the mordant copolymers as self-associated aggregates and contribute importantly to desired water insensitivity of the image-receiving layer. Inasmuch as the Formula-I copolymer mordants include a vinylbenzyl quaternary ammonium water-solubilizing functionality, the mordants can be coated from aqueous media. Desired physical attributes (e.g., reduced water swellability) of the coated image-receiving layer can be controlled by the content of the vinylbenzyl thymine (or uracil) derivative in the copolymeric mordant and by the self-aggregation promoted by the aforementioned multiple H-bonding sites. Suitable relative proportions of the respective Formula-II and Formula-III components can be selected for control of the properties contributed by the respective compounds and according to predetermined desired properties. It can be seen from the inspection of the Formula-III vinylbenzyl thymine (or uracil) compounds that the compounds contain unsaturation at positions 5 and 6 of the heterocyclic ring. Such unsaturation provides photoreactivity, allowing for 2+2 cyclization, and permits control of the physical properties of the copolymeric mordant by photoirradiation (typically, in the ultraviolet region) and cyclization. Thus, a copolymeric mordant of the invention, coated to a suitable image-receiving layer in the image-receiving element of the invention, can be subjected to a radiation treatment to promote cyclization (cross-linking) and increased water insensitivity. The cross-linking reaction can be employed as a means of reducing swellability of the image-receiving layer and to thereby promote the realization of higher D.sub.max dye densities than may otherwise be attainable.
The relative proportions of the recurring units represented by the integers a and b in Formula-I, as indicated previously, can vary over a wide range (e.g., in the molar range of 10:1 to 1:10). In general, such proportions will be dependent upon the particular mordant ("a") component and its mordanting capacity and on the desired control of the physical properties of the mordant and image-receiving layer, promoted by H-bonding self-aggregation and/or irradiation treatment, which control will be dictated by the relative proportion of the vinylbenzyl thymine or uracil ("b") component of the mordant. It will be appreciated, for example, that photocrosslinking greater in amount than may be beneficial from the standpoint of maximization of D.sub.max values may be desired where certain physical attributes, e.g., water insensitivity and image-receiving layer durability, are desired in a particular photographic system.
Those skilled in the art can utilize the photoreactivity of the vinylbenzyl thymine (and uracil) units to achieve a desirable balance of properties suited to a particular photographic product and system. For example, a molar ratio of 2.5:1 to 9:1 can be used for a desired balance of mordanting and image-receiving layer physical properties. Good results are obtained, for example, using a preferred 4:1 ratio of units from the vinylbenzyl quaternary ammonium salt and from the VBT monomer. Such a copolymeric mordant can be conveniently coated in the formation of an image-receiving layer providing the mordanting sites for efficient dye mordanting without excessive coating or coverage requirements.
It will be appreciated that within the aforesaid molar proportions, changes in relative molar proportions of the respective recurring units will influence the physical and functional properties of he copolymeric mordants. Thus, differences in alkali solubility or swellability, alkali permeability, hydrophilic-hydrophobic balance, coatability of the copolymeric mordant or receptivity of the copolymeric mordant to one or more dyes may be observed. It should be understood that obtainable benefits will be dependent upon the proportion of VBT units in the copolymer, the proportion of the copolymer in the image-receiving layer, and the nature of permeator polymers (e.g., gelatin or PVA).
The copolymeric mordants of the present invention can be prepared by the polymerization in suitable proportions of the vinylbenzyl quaternary ammonium salt and the VBT monomer set forth hereinbefore. The polymerization can be conducted by resort to bulk, solution, suspension or emulsion techniques. The polymerization can be initiated chemically, as by the utilization of a suitable free-radical polymerization initiator or redox initiator. Suitable free-radical initiators include the water-soluble or alcohol-soluble azo-type initiators such as 4,4'-azobis-4(cyanovaleric acid), azobisisobutyronitrile, diazoaminobenzene and 2,2'-azobis (2-amidinopropane) hydrochloride. Suitable redox-type polymerization initiators include a combination of a reducing agent such as sodium bisulfite, ascorbic acid or ferrous salt and an oxidizing agent such as benzoyl peroxide, ammonium persulfate, hydrogen peroxide, diacetyl peroxide, t-butyl hydroperoxide or an alkali metal persulfate. The amount of catalyst employed can be varied to suit particular needs. In general, satisfactory polymerization reactions can be conducted over a temperature range of from about 25.degree. C. to about 100.degree. C. utilizing less than about 5% by weight of the initiator, based upon the weight of the copolymerizable monomers.
Suitable examples of copolymeric mordants useful in the image-receiving elements of the invention, and methods for their preparation, are described in the patent application of J. Michael Grasshoff, et al., for VINYLBENZYL THYMINE MONOMERS AND POLYMERS AND PRODUCTS PREPARED FROM SAME, filed of even date, the contents of which are incorporated herein by reference.
The copolymeric mordant materials of the present invention can be utilized for the provision of an image-receiving layer for photographic images in dye, and, in particular, for the provision of multicolor dye images. The copolymeric mordant material of the invention can alone comprise the image-receiving layer or can be employed in admixture with other polymeric materials to comprise an image-receiving layer. Particularly preferred is an image-receiving layer comprising a mixture or blend of a copolymeric mordant material of the invention, as hereinbefore described, with other known polymeric image-receiving layer materials, particularly hydrophilic polymeric permeator materials such as gelatin, polyvinylalcohol, polyvinylpyrrolidones, and mixtures of these. The materials utilized in admixture with the copolymeric mordant material hereof and the relative amounts of each can depend, for example, on the nature and amount of dye desirably mordanted and upon the permeability of the image receiving layer to an aqueous alkaline processing composition. Particularly preferred image-receiving layers comprise a mixture of the copolymeric mordant hereof and polyvinylalcohol where the ratio by weight of polyvinylalcohol to the copolymeric mordant hereof is about 0.2:1 to about 3:1. For example, good results are realized using a 2/1 weight ratio of copolymeric mordant and polyvinylalcohol such as "Vinol 350" and "Airvol 165" (Air Products and Chemicals, Inc.) and "Elvanol 9050" (E.I. dupont de Nemours).
An image-receiving element of the invention which includes a copolymeric mordant as hereinbefore described can be photoirradiated for control of physical properties, using conventional lamp sources and irradiation techniques. Thus, in the manufacture of an image-receiving element of the invention, the image-receiving layer component thereof will be applied, typically, from an aqueous medium and will be then dried and subjected to an irradiation treatment. The amount of irradiation and the duration of the irradiation treatment will depend upon the particular mordant copolymer, the proportion thereof in the image-receiving layer, and especially, the relative content of the VBT component of the copolymer mordant.
A suitable irradiation treatment can be effected using conventional sources of ultraviolet radiation, such as carbon arc lamps, "D" bulbs, Xenon lamps and high-pressure mercury lamps. It will be appreciated that desired insolubilization promoted by photocyclization will permit control of the water swellability of the image-receiving later during photographic processing, thereby promoting high D.sub.max dye density values. The amount of cross-linking should, however, be such as to permit a desired balance of good dye density D.sub.max values and rates of dye transfer, along with desired physical (e.g., controlled swellability and water insensitivity) properties. Optimal irradiation treatment can be determined for a particular image-receiving element and photographic product and system, consistent with the above objectives.
Image-receiving layers comprising the copolymeric mordants of this invention can be utilized, for example, in image-receiving elements designed to receive and mordant image dye-providing materials. Such image-receiving elements will generally comprise a suitable support carrying an image-receiving layer comprising a copolymeric mordant of this invention and may also include one or more polymeric acid-reacting layers such as those described, for example, in U.S. Pat. No. 3,362,819. These polymeric acids can be polymers which contain acid groups, e.g., carboxylic acid and sulfonic acid groups, which are capable of forming salts with alkali metals or with organic bases; or potentially acid-yielding groups such as anhydrides or lactones. The polymeric acid-reacting layer functions to reduce the environmental pH of a diffusion transfer system in which the image-receiving layer is utilized and, thereby, provides the advantages and benefits thereof known in the art.
A spacer layer may be disposed between the polymeric acid layer and the image-receiving layer in order to control the pH reduction so that it is not premature, e.g., to "time" control the pH reduction. Suitable spacer of "timing" layers for this purpose are described for example, in the U.S. Pat. Nos. 3,362,819; 3,419,398; 3,431,893; 3,433,633; 3,455,686; 3,575,701; and 3,756,815.
Referring to FIG. 1, there is shown an image-receiving element of the invention 10 comprising support material 12 carrying a layer of acid-reacting polymer 14, a timing layer 16, and image-receiving layer 18 comprising a copolymeric mordant of the invention and optional overcoat layer 20. Support material 12 can comprise any of a variety of materials capable of carrying image-receiving layer 18 and other layers as shown in FIG. 1. Paper, vinyl chloride polymers, polyamides such as nylon, polyesters such as polyethylene glycol terephthalate or cellulosic derivatives such as cellulose acetate or cellulose acetate-butyrate can be suitably employed. It will be appreciated that depending upon the particular application intended for image-receiving element 10, the nature of support material 12 as a transparent, opaque or translucent material will be a matter of choice.
According to one embodiment of the present invention, image-receiving element 10 can comprise support material 12 on which is present image-receiving layer 18. Polymeric acid-reacting layer 14 and timing layer 16, each shown in FIG. 1, need not be present in image-receiving element 10, and where such an image-receiving element is utilized in a photographic diffusion transfer product or process, polymeric acid-reacting and timing layers 14 and 16, respectively, can be otherwise suitably positioned in such product or process as will be apparent from the film unit of FIG. 3, described in greater detail hereinafter. According to one embodiment, image-receiving element 10 will include polymeric acid-reacting and timing layers, shown, respectively, in FIG. 1 as layers 14 and 16. The nature and function of such layers in diffusion transfer products and processes is known and described in greater detail hereinafter.
As indicated previously, support 12 of image-receiving element or article 10 can be suitably transparent, opaque or translucent depending upon a particular application of the element or article. Thus, where image-receiving element 10 is desirably utilized in the manufacture of photographic diffusion transfer film units such as shown generally in FIGS. 2 and 3 hereof, where the desired image will be viewed through a support, support 12 will be of transparent material. A preferred material for this purpose is a polyethylene glycol terephthalate sheet-like support material. Alternatively, where image-receiving element 10 is utilized in the manufacture of a photographic film unit such as is generally shown in FIG. 4, where the desired image will be viewed as a reflection print against a light-reflecting layer, support material 12 will preferably be of opaque material.
In FIG. 1 is shown overcoat layer 20 which comprises an optional layer of image-receiving element 10. Image-receiving layer 18 can, thus, comprise the outermost layer of image-receiving element 10. In some instances, it may be desirable to provide such image-receiving layer 18 with a washing treatment, as by washing the layer with ammonia. The washing treatment can be conveniently effected with ammonia or a solution of ammonium hydroxide in a concentration, preferably of from about 2% to about 8% by weight. Such ammonia washing treatment effectively neutralizes residual acrolein/formaldehyde condensate where such material is utilized for the hardening of the image-receiving layer and the provision of reduced water sensitivity. According to one embodiment of the invention, as shown in FIG. 1, an overcoat layer 29 can be present on image-receiving layer 18. Such-overcoat layer can be comprised of a polymeric material such as polyvinyl alcohol.
Overcoat layer 20 can also be utilized as a means of facilitating separation of image-receiving element 10 from a photosensitive element. Thus, where the image-receiving element is utilized in a photographic film unit which is processed by distribution of an aqueous alkaline processing composition between the image-receiving element and a photoexposed photosensitive element and is adapted, after formation of a dye image, to separation from the developed photosensitive element and the processing composition, overcoat layer 20 can effectively function as a "strip coat".
An overcoat suited as a "strip coat" can be prepared from a variety of hydrophilic colloid materials. Suitable hydrophilic colloids for an overcoat or "strip coat" for a diffusion transfer image-receiving element requiring separation, subsequent to formation of a transfer image from a processing composition, include gum arabic, carboxymethyl cellulose, hydroxyethyl cellulose, carboxymethyl hydroxyethyl cellulose, cellulose acetate-hydrogen phthalate, polyvinyl alcohol, polyvinyl pyrrolidone, methyl cellulose, ethyl cellulose, cellulose nitrate, dium alginate, pectin, polymethacrylic acid, polymerized salts of alkyl, aryl and alkyl sulfonic acids (e.g., Daxad, W. R. Grace Co.), and the like.
Overcoat 20 can comprise a solution of hydrophilic colloid and ammonia and can be coated from an aqueous coating solution prepared by diluting concentrated ammonium hydroxide (about 28.7% NH.sub.3) with water to the desired concentration, preferably from about 2% to about 8% by weight, and then adding to this solution an aqueous hydrophilic colloid solution having a total solids concentration in the range of about 1% to about 5% by weight. The coating solution also preferably may include a small amount of a surfactant, for example, less than about 0.10% by weight of Triton X-100 (Rohm and Haas Co., Phila., Pa.). A preferred solution comprises about 3 parts by weight of ammonium hydroxide and about 2 parts by weight of gum arabic.
The image-receiving layers of the present invention find applicability in a number of photographic diffusion transfer products and processes. According to one embodiment of the present invention, the image-receiving layers of the invention are utilized in photographic film units adapted to the provision of photographs comprising the developed silver halide emulsion(s) retained as part of a permanent laminate, with the desired image being viewed through a transparent support against a reflecting background. In such photographs, the image-carrying layer is not separated from the developed silver halide emulsion(s). Diffusion transfer photographic products providing an image viewable without separation against a reflecting background in such a laminate have been referred to in the arts as "integral negative-positive film units".
Integral negative-positive film units of a first type are described, for example, in the above-noted U.S. Pat. No. 3,415,644 and include appropriate photosensitive layer(s) and image-dye-providing materials carried on an opaque support, an image-receiving layer carried on a transparent support and means for distributing a processing composition between the elements of the film unit. Photoexposure is made through the transparent support carrying a polymeric acid-reacting layer, a timing layer and the image-receiving layer of the invention. A processing composition containing a reflecting pigment is distributed between the image-receiving and photosensitive components. After distribution of the processing composition and before processing is complete, the film unit can be, and usually is, transported into light. Accordingly, in integral negative-positive film units of this type, the layer provided by distributing the reflecting pigment provides a reflecting background for viewing through the transparent support the image transferred to the image-receiving layer.
Integral negative-positive film units of a second type, as described, for example, in U.S. Pat No. 3,594,165, include a transparent support, carrying the appropriate photosensitive layers and associated image dye-providing materials, a permeable opaque layer, a permeable and preformed light-reflecting layer, and means for distributing a processing composition between the photosensitive layer and a transparent cover or spreader sheet carrying a polymeric acid-reacting layer and a timing layer. Integral negative-positive film units of this second type include an opaque processing composition which is distributed after photoexposure to provide a second opaque layer which can prevent additional exposure of the photosensitive element. In film units of this second type, exposure is made though the transparent cover or spreader sheet. The desired transfer image is viewed against the reflecting pigment-containing layer through the transparent support element.
The arrangement and order of the individual layers of the diffusion transfer film units described herein may vary in many ways as is known in the art, provided the film units comprise an image-receiving layer comprising a copolymeric mordant of the invention. For convenience, however, the more specific descriptions of the invention hereinafter set forth will be by use of dye developer diffusion transfer color processes and of diffusion transfer film units of the type generally contemplated in previously mentioned patents. Thus, details relating to integral negative-positive film units of the first type described hereinbefore can be found in such patents as U.S. Pat. Nos. 3,415,644 and 3,647,437 while details of the second type are found in U.S. Pat. No. 3,594,165. It will be readily apparent from such descriptions that other image-forming reagents may be used, e.g., color couplers, coupling dyes, or compounds which release a diffusible dye or dye intermediate as a result of coupling or oxidation.
Referring now to the drawings, FIG. 2 shows a film unit of the type described in referenced U.S. Pat. Nos. 3,415,644 and 3,657,437 following exposure and processing. The film unit 30 includes a polymeric acid-reacting layer 34, timing layer 36 and image-receiving layer 38 comprising a mordant copolymer of the invention. After photoexposure of photosensitive layer(s) 42 (through transparent support 32, polymeric acid-reacting layer 34, timing layer 36 and image-receiving layer 38) the processing composition retained in a rupturable container (not shown) is distributed between layers 38 and 42. Processing compositions used in such film units of the present invention are aqueous alkaline photographic processing compositions comprising a reflecting pigment, usually titanium dioxide, and a polymeric film-forming agent and will preferably contain an optical filter agent described in detail in U.S. Pat. No. 3,647,437.
Distribution of the processing composition over photoexposed portions of photosensitive system 42 provides a light-reflecting layer 40 between image-receiving layer 38 and photosensitive layer(s) 42. This layer, at least during processing, provides sufficient opacity to protect photosensitive system 42 from further photoexposure through transparent support 32. As reflective layer 40 is installed, by application of the processing composition, development of photoexposed photosensitive layer(s) 42 is initiated to establish in manners well-known in the art an imagewise distribution of diffusible image-providing material which can comprise soluble silver complex or one or more dye or dye intermediate image-providing materials. The diffusible image-providing material is transferred through permeable, light-reflecting layer 40 where it is mordanted, precipitated or otherwise retained in or on image-receiving layer 38 of the invention. The resulting transfer image is viewed through transparent support 32 against light-reflecting layer 40.
The light-reflecting layer 40 provided by the embodiment of the invention shown in FIG. 2 is formed by solidification of the stratum of processing composition distributed after exposure. The processing composition will include the film-forming polymer which provides the polymeric binder matrix of the light-reflecting pigment of layer 40. Absorption of water from the applied layer of processing composition results in a solidified film comprising the polymeric binder matrix and the pigment material, thus providing the light-reflecting layer 40 which permits the viewing thereagainst of image 38 through transparent support 32. In addition, light-reflecting layer 40 serves to laminate together the developed photosensitive system 42 and the image-bearing layer 38 to provide the final photographic laminate.
In each of articles 10 and 30, respectively, of FIGS. 1 and 2 and in articles 50 and 70, respectively, of FIGS. 3 and 4, is shown a polymeric acid-reacting layer. In each instance, the polymeric acid-reacting layer, e.g., layer 14 of image-receiving element 10, provides important functions in photographic processing. The processing compositions typically employed in diffusion transfer processes of the type contemplated herein will generally comprise an aqueous alkaline composition having a pH in excess of about 12, and frequently in the order of 14 or greater. The liquid processing composition permeates the emulsion layer(s) of the photosensitive element to effect development thereof. The elevated environmental pH conditions of the film unit upon spreading or distribution of the alkaline processing composition are conducive to transfer of image dyes. The acid-reacting layer, for example, polymeric acid-reacting layer 14 of image-receiving element 10 or polymeric acid-reacting layer 34 of film unit 30, is, thus, employed to lower in predetermined manner the environmental pH of the film unit following substantial dye transfer in order to increase image stability and/or adjust the pH from a first pH at which the image dyes are diffusible to a second and lower pH at which such image-dyes are not diffusible. Simultaneously, the reduction of pH permits discoloration of opacification dyes utilized in the film unit to provide inlight development capability.
As disclosed in, for example, U.S. Pat. No. 3,362,819, the polymeric acid-reacting layer may comprise a nondiffusible acid-reacting reagent adapted to lower the pH from the first (high) pH of the processing composition in which the image dyes are diffusible to a second (lower) pH at which they are not. The acid-reacting reagents are preferably polymers which contain acid groups, e.g., carboxylic acid and sulfonic acid groups, which are capable of forming salts with alkali metals or with organic bases; or potentially acid-yielding groups such as anhydrides or lactones. Preferably, the acid polymer contains free carboxyl groups. As examples of useful neutralizing layers, in addition to those disclosed in the aforementioned U.S. Pat. No. 3,362,819, mention may be made of those disclosed in the following U.S. Pat. Nos.: Bedell, U.S. Pat. No. 3,765,885; Sahatjian, et al., U.S. Pat. No. 3,819,371; Haas, U.S. Pat. No. 3,833,367; Taylor U.S. Pat. No. 3,754,910 and Schlein, U.S. Pat. No. 3,756,815.
In each of the articles shown in FIGS. 1 to 4 is shown a timing layer which is included for the control of the pH-reducing properties of the polymeric acid-reacting layer. Thus, there is shown in FIG. 2 timing layer 36 positioned between polymeric acid-reacting layer 34 and image-receiving layer 38 of the invention. The spacer layer will be comprised of polyvinyl alcohol, gelatin or other polymer through which the alkali may diffuse to the polymeric acid-reacting layer. The presence of such a timing layer between the image-receiving layer 38 and the acid-reacting layer 34 effectively controls the initiation and the rate of capture of alkali by the acid-reacting layer. Suitable materials for the formation of timing layers and the advantages thereof in diffusion transfer systems are described with particularity in U.S. Pat. Nos. 3,362,819; 3,419,389; 3,421,893; 3,455,686; 3,577,237; and 3,575,701.
In the film unit shown in FIG. 2, polymeric acid-reacting layer 34 and the timing layer 36 are shown on transparent support 32. If desired, layers 34 and 36 can be positioned between opaque support 44 and photosensitive layer(s) 42. Thus, polymeric acid-reacting layer 34 can be positioned on opaque support 44 and timing layer 36 can be positioned on the polymeric acid-reacting layer. In turn, the emulsion layer(s) comprising photosensitive system 42 can be positioned on the timing layer. In this case, image-receiving element 32a will comprise transparent support 32, and directly thereon, image-receiving layer 38. The utilization of polymeric acid-reacting and timing layers in a photosensitive element as aforedescribed is described in U.S. Pat. Nos. 3,362,821 and 3,573,043.
In accordance with one embodiment of the invention, a photographic film unit can comprise a temporary laminate including the several layers of the photographic film unit confined between two dimensionally stable supports and having the bond between a predetermined pair of layers being weaker than the bond between other pairs of layers. Thus, with reference to FIG. 2, an image-receiving element 32a, comprising transparent support 32, polymeric acid-reacting layer 34, timing layer 36 and image-receiving layer 38 and corresponding generally to image-receiving element 10 of FIG. 1, can be arranged in article 30 such that image-receiving layer 38 is temporarily bonded to the silver halide emulsion layer 42 prior to exposure. The rupturable container or pod (not shown) can then be positioned such that, upon its rupture, the processing composition will delaminate the temporary bond and be distributed between the aforesaid layers 38 and 42. The distributed layer of processing composition upon drying forms light-reflecting layer 40 which serves to bond the layers together to form the desired permanent laminate. Procedures for forming such prelaminated film units, i.e., film units in which the several elements are temporarily laminated together prior to exposure, are described, for example, in U.S. Pat. No. 3,652,281, issued to Albert J. Bachelder and Frederick J. Binda and in U.S. Pat. No. 3,652,282 to Edwin H. Land both issued Mar. 28, 1972. A particularly useful and preferred prelamination utilizes a water-soluble polyethylene glycol as described and claimed in U.S. Pat. No. 3,793,023, issued Feb. 19, 1974 to Edwin H. Land.
If desired, the film unit shown in FIG. 2 may utilize a transparent support instead of the opaque support 44 shown therein. In accordance with this alternative embodiment, an opaque layer, e.g., pressure-sensitive, should be superposed over said transparent support to avoid further exposure through the back of the film unit during processing outside of the camera. In the embodiment illustrated in FIG. 2, photoexposure is effected through the image-receiving embodiment, it will be understood that the image-receiving element may be initially positioned out of the exposure path and superposed upon the photosensitive element after photoexposure, in which event the processing and final image stages would be the same as in FIG. 2.
In FIG. 3 is shown, following exposure and processing, as second integral negative-positive type of diffusion transfer film unit of the invention utilizing an arrangement of elements generally described in U.S. Pat. No. 3,594,165 and British Pat. No. 1,330,524. Such arrangement provides an integral negative-positive reflection print and photoexposure and viewing are effected from opposite sides. Film unit 50 includes a processing composition initially retained in a rupturable container (not shown) arranged to distribute the processing composition between photosensitive system or layer 60 and a cover or spreader sheet 68a comprising a transparent sheet material 68, polymeric acid-reacting layer 66 and timing layer 64. Spreader sheet 68a facilities uniform distribution of processing composition after photoexposure of photosensitive system or layer 60 which is effected through transparent sheet material 68. Processing compositions used in such film units are aqueous, alkaline photographic processing compositions which include a light-absorbing opacifying agent, e.g., carbon black.
Distribution of the processing composition between photoexposed photosensitive system or layer 64 and spreader sheet 68a installs an opaque layer 62 which protects system or layer 60 from further photoexposure through transparent spreader sheet 68a. Like the film units of FIG. 3, as and after opaque layer 62 is installed, the processing composition initiates development of photoexposed photosensitive system or layer 60 to establish an imagewise distribution of diffusible image-providing material in manners well-known to the art. For example, the processing composition may contain developing agents sufficient to effect photographic development. Alternatively, developing agents may be present in one or more layers of the film unit so that they may be carried to system or layer 60 by the processing composition. The diffusible imagewise distribution is transferred to image-receiving layer 54 through permeable light-reflecting layer 56 which comprises a preformed layer including a light-reflecting pigment. Film units of the type shown in FIG. 3 may also comprise a preformed and permeable opaque layer 58 including a light-absorbing pigment, e.g., a dispersion of carbon black in polymer permeable to the processing composition. Such layer, between photosensitive system or layer 60 and light-reflecting layer 56, permits in-light development of film unit 50, providing opacification for the protection of photoexposure system or layer 60 against further exposure through transparent support 52 and layers 54 and 56. The transfer image is viewed through transparent support 52 against light-reflecting layer 56.
The image-receiving layers of the present invention can be utilized in so-called "peel-apart" diffusion transfer film units designed to be separated after processing. Such a diffusion transfer film unit of the invention is shown in FIG. 4 as film unit 70. The film unit shown in FIG. 4 comprises a photosensitive element 72a comprising an opaque support 72 carrying a photosensitive layer or system 74. In film units of this type, the photosensitive layer or system 74 is photoexposed and a processing composition 76 is then distributed over the photoexposed layer or system. An image-receiving element 86a, corresponding generally to image-receiving element 10 of FIG. 1, is superposed on the photoexposed photosensitive element. As shown in FIG. 4, image-receiving element 86a comprises an opaque support material 88, and a light-reflecting layer 86, against which the desired transfer image is viewed and which typically will comprise a polymeric matrix containing a suitable white pigment material, e.g., titanium dioxide. A polymeric acid-reacting layer 84 is shown positioned on light-reflecting layer 86 on which is shown timing layer 82, the image-receiving layer 80 of the invention and, in turn, overcoat layer 78, each of which layers is comprised of materials described hereinbefore in connection with the articles and film units shown in FIGS. 1 to 3. Like the film units shown in FIGS. 2 and 3, the processing composition permeates photoexposed photosensitive layer or system 74 to provide an imagewise distribution of diffusible dye image-providing material which is transferred at least in part to image-receiving layer 78. Unlike the film units of FIGS. 2 and 3, however, the transferred dye image is viewed in image-bearing layer 80 against light-reflecting layer 86 after separation of image-receiving element 86a from photosensitive element 72a.
While support material 88 of image-receiving element 86a is shown as being of opaque material, it will be appreciated that a transparent support material can be employed and that the film unit can be processed in the dark or an opaque sheet (not shown), preferably pressure-sensitive, can be applied over such transparent support to permit inlight development. In accordance with a preferred embodiment of the invention, whereby a reflection print is provided upon separation of image-receiving element 86a from photosensitive element 72a, opaque support 88 and light-reflecting layer 86 will comprise, for example, a suitable paper support, coated, preferably on both sides, with a polymeric coating, e.g., polyethylene, pigmented with titanium dioxide. Such a support material can be suitably provided with polymeric acid-reacting layer 84, a timing layer 82, an image-receiving layer 80 of the invention and optional overcoat layer 78, as shown in FIG. 4 with formation of image-receiving element 86a.
It will be appreciated that, where a transparency is desirably provided from film unit 70 of FIG. 4, support 88 can be transparent and light-reflecting layer 86 omitted. The desired image in image-bearing layer 80 can then, upon separation of image-receiving element 86a from photosensitive element 72a, be viewed as a positive transparency through transparent support material 88.
The film units illustrated in FIGS. 2 to 4 have, for convenience, been shown as monochrome film. Multicolor images may be obtained by providing the requisite number of differentially exposable silver halide emulsions, and said silver halide emulsions are most commonly provided as individual layers coated in superposed relationship. Film units intended to provide multicolor images comprise two or more selectively sensitive silver halide layers each having associated therewith an appropriate image dye-providing material providing an image dye having spectral absorption characteristics substantially complementary to the light by which the associated silver halide is exposed. The most commonly employed negative components for forming multicolor images are of the "tripack" structure and contain blue-, green-, and red-sensitive silver halide layers each having associated therewith in the same or in a contiguous layer a yellow, a magenta and a cyan image dye-providing material, respectively. Interlayers or spacer layers may, if desired, be provided between the respective silver halide layers and associated image dye-providing materials or between other layers. Integral multicolor photosensitive elements of this general type are disclosed in U.S. Pat. No. 3,345,163 issued Oct. 3, 1967, to Edwin H. Land and Howard G. Rogers, as well as in the previously noted U.S. patents, e.g., in FIG. 9 of the aforementioned U.S. Pat. No. 2,983,606.
The image dye-providing materials which may be employed in such processes generally may be characterized as either (1) initially soluble or diffusible in the processing composition, but are selectively rendered non-diffusible in an imagewise pattern as a function of development; or (2) initially insoluble or non-diffusible in the processing compositions, but which are selectively rendered diffusible or provide a diffusible product in an imagewise pattern as a function of development. These materials may be complete dyes or dye intermediates, e.g., color couplers. The requisite differential in mobility or solubility may, for example, be obtained by a chemical action such as a redox reaction or a coupling reaction.
As examples of initially soluble or diffusible materials and their application in color diffusion transfer, mention may be made of those disclosed, for example, in U.S. Pat. Nos. 2,774,668; 2,968,554; 2,983,606; 2,087,817; 3,185,567; 3,230,082; 3,345,163; and 3,443,943. As examples of initially non-diffusible materials and their use in color transfer systems, mention may be made of the materials and systems disclosed in U.S. Pat. Nos. 3,185,567; 3,443,939; 3,443,940; 3,227,550; and 3,227,552. Both types of image dye-providing substances and film units useful therewith also are discussed in U.S. Pat. No. 3,647,437 to which reference may be made.
The image-receiving layers of the invention, as indicated hereinbefore, provide certain advantages in photographic diffusion transfer products and processes. Thus, an image-receiving element of the invention comprising a mordant copolymer hereof permits the realization of good maximum dye densities. It has been found, for example, that a 4:1 mole ratio copolymer of vinylbenzyl trimethyl ammonium chloride and VBT, in general, provides a higher level of maximum density (D.sub.max) values than a homopolymer of vinylbenzyl trimethyl ammonium chloride.
The following examples are illustrative of the present invention and it will be understood that the invention is not limited thereto. All parts and percentages are by weight, except as otherwise indicated. In each of the EXAMPLES hereof, the vinylbenzyl trimethyl ammonium chloride monomer utilized in the polymerization was a mixture predominantly of para and meta isomers additionally containing a small content of ortho isomer. Accordingly, the molecular structure provided in the examples as indicative of the structure of recurring units from vinylbenzyl trimethyl ammonium chloride shows, for convenience, the positioning of the quaternary ammonium moiety without positional specificity to reflect the utilization of such a mixture of positional isomers.
EXAMPLE I
In a 2-L 3-neck round bottom flask, equipped with stirrer, reflux condenser and addition funnel, water and aqueous KOH are mixed, followed by addition of thymine, 60 g (0.476 mol) at ambient temperature to give a clear solution. The rate of agitation is increased and EtOH is added over a period of ten minutes resulting in a fine dispersion of thymine potassium salt. Upon addition of the inhibitor (2,6-di-t-butyl-4-methylphenol, 0.3 g) and 73 g 0.478 mol) vinylbenzyl chloride (Dow Chemical, a 60/40 m/p isomer mixture), the batch is heated at gentle reflux for 6 hours and subsequently allowed to cool to room temp. Vacuum filtration (to remove KCl) renders a clear, slightly yellow solution which is subjected to solvent evaporation under reduced pressure (<30.degree. C.) to yield a semi-solid residue. The product is taken up in 500 ml of warm toluene, followed by filtration to remove undissolved solid (consisting mostly of unreacted thymine). A small amount of high r.sub.f material (presumably dissolved thymine) is then removed by passing the toluene solution through a 1-inch layer of silica (placed on a coarse sintered-glass funnel). The filtrate is concentrated to about half its volume. To the heated pre-purified toluene solution is gradually added with stirring about 200 ml of hexane and the slightly cloudy mixture is allowed to cool to room temp. Seed crystals from a previous run are preferably added before transferring the batch to a refrigerator. Complete crystallization is attained after refrigeration for 24 hours. The slightly yellow crystals are filtered and washed with toluene/hexane 5:1 (v/v) and finally hexane. After recrystallization form toluene/hexane, 2:1 (v/v), and subsequent vacuum drying at room temperature, about 50 g of the pure compound is obtained, 45-50%, mp 110.degree. C. The monomer had the following structure ##STR7##
EXAMPLE II
A solution of vinylbenzyl trimethyl ammonium chloride (TMQ) (3.5 g, 0.017 tool) and 1-VBT (1 g, 0.004 mol) was prepared in 2-propanol (40 ml). After adding 0.02 of AIBN, the solution was heated under nitrogen for 16 hrs. at 65.degree. C., during which time the copolymer precipitated. The copolymer had the following structure: ##STR8##
EXAMPLE III
An image-receiving element was prepared comprising the following layers coated in succession on a white-pigmented polyethylene coated opaque support:
1. a polymeric acid-reacting layer, at a coverage of about 2390 mg/ft.sup.2 (about 25726 mg/m.sup.2), comprising 9 parts Gantrez S-97 (from GAF Corp.), a free acid of a copolymer of methyl vinyl ether and maleic anhydride and 11 parts Airflex 465 vinyl acetate/ethylene latex copolymer (Air Products and Chemicals, Inc.);
2. a timing layer coated at a coverage of about 250 mg/ft.sup.2 (about 2691 mg/m.sup.2) comprising a copolymer of diacetone acrylamide and acrylamide grafted onto polyvinyl alcohol;
3. a hold-release timing layer coated at a coverage of about 235 mg/ft.sup.2 (about 2529 mg/m.sup.2) comprising a copolymer of diacetone acrylamide/butyl acrylate/carboxymethoxymethyl acrylate/methacrylic acid;
4. an image-receiving layer coated at a coverage of about 300 mg/ft.sup.2 (about 3229 mg/m.sup.2) of a 2:1 mixture of vinyl benzyl trimethylammonium chloride (TMQ) and polyvinyl alcohol; and
5. a strip coat layer coated at a coverage of about 68 mg/ft.sup.2 (about 926 mg/m.sup.2) of gum arabic.
This image-receiving element was used as a means of establishing a comparative evaluation with image-receiving elements according to the invention and is identified herein as CONTROL.
EXAMPLE IV
Image-receiving elements (A-E) according to the invention were prepared. These were the same as the CONTROL with the exception that, in lieu of the image-receiving layer of the CONTROL, the following image-receiving layer, respectively, was in each instance employed:
Image-Receiving Element A--an image-receiving layer coated at a coverage of about 300 mg/ft.sup.2 (about 3229 mg/m.sup.2) of a 2:1 mixture of the 80/20 TMQ/VBT copolymer and polyvinyl alcohol (Vinol 350, Air Products and Chemicals, Inc.);
Image-Receiving Element B--an image receiving layer coated at a coverage of about 300 mg/ft.sup.2 (about 3229 mg/m.sup.2) of a 2:1:0.5 mixture of the 80/20 TMQ/VBT copolymer, polyvinyl alcohol (Vinol 350), and dimethyl hydantoin formaldehyde;
Image-Receiving Element C--an image receiving layer coated at a coverage of about 300 mg/ft.sup.2 (about 3229 mg/m.sup.2) of a 2:1:0.15 mixture of the 80/20 TMQ/VBT copolymer, polyvinyl alcohol (Vinol 350), and glyoxal;
Image-Receiving Element D--an image-receiving layer coated at a coverage of about 300 mg/ft.sup.2 (about 3229 mg/m.sup.2) of a 2:1:0.01 mixture of the 80/20 TMQ/VBT copolymer, polyvinyl alcohol (Vinol 350), and boric acid; and
Image-Receiving Element E--an image-receiving layer coated at a coverage of about 300 mg/ft.sup.2 (about 3229 mg/m.sup.2) of a 2:1:0.1 mixture of the 80/20 TMQ/VBT copolymer, deionized bone gelatin, and succindialdehyde.
EXAMPLE V
The image-receiving elements of EXAMPLES III and IV were evaluated in photographic film units of the "peel-apart" type in the following manner:
A photosensitive element was utilized for the processing and evaluation of each of the image-receiving elements. The photosensitive element comprised an opaque subcoated polyethylene terephthalate photographic film base having the following layers coated thereon in succession:
1. a layer of sodium cellulose sulfate at a coverage of about 9 mg/m.sup.2 ;
2. a cyan dye developer layer comprising about 816 mg/m.sup.2 of the cyan dye developer represented by the formula ##STR9## about 100 mg/m.sup.2 of N.sub.1 N.sup.1 -[(1,2,3,4-tetrahydro-5,8-dihydroxy-1,4-methanonaphthalene-6,7-diyl)bis(methylene)]bisacetamide; and about 412 mg/m.sup.2 of gelatin;
3. a red-sensitive silver iodobromide layer comprising about 367 mg/m.sup.2 of silver (0.7 micron), about 367 mg/m.sup.2 of silver (1.5 microns) and about 550 mg/m.sup.2 of gelatin;
4. an interlayer comprising about 2422 mg/m.sup.2 of a 96:4 blend of a 60/29/6/4/0.4 pentapolymer of butyl acrylate/diacetone acrylamide/methacrylic acid/styrene/acrylic acid and polyacrylamide, about 124 mg/m.sup.2 of dantoin and about 3 mg/m.sup.2 of succindialdehyde;
5. a magenta dye developer layer comprising about 374 mg/m.sup.2 of a magenta dye developer represented by the formula ##STR10## about 199 mg/m.sup.2 of gelatin, about 199 mg/m.sup.2 of 2-phenyl benzimidazole; and about 30 mg/m.sup.2 of cyan filter dye and about 197 mg/m.sup.2 of gelatin;
6. a polymeric layer comprising about 50 mg/m.sup.2 of carboxylated styrene/butadiene copolymer latex (Dow 620 latex), 133 mg/m.sup.2 of titanium dioxide, 50 mg/m.sup.2 of a 60/29/6/4/0.04 pentapolymer of butyl acrylate/diacetone acrylamide/methacrylic acid/styrene/acrylic acid, and about 17 mg/m.sup.2 of gelatin;
7. a green-sensitive silver iodobromide layer comprising about 358 mg/m.sup.2 of silver (0.6 micron), about 4 mg/m.sup.2 of silver (1.3 microns) and about 286 mg/m.sup.2 of gelatin;
8. a layer comprising about 715 mg/m.sup.2 of N.sub.1 N.sup.1 -(1,2,3,4-tetrahydro-5,8-dihydroxy-1,4-methanonaphthalene-6,7-diyl)bis(methylene)]bisacetamide and about 286 mg/m.sup.2 of gelatin;
9. an interlayer comprising about 1524 mg/m.sup.2 of a 95:5 mixture of the 60/29/6/4/0.4 pentapolymer of butyl acrylate/diacetone acrylamide/methacrylic acid/styrene/acrylic acid and of polyacrylamide, and about mg/m.sup.2 of succindialdehyde;
10. a layer comprising about 900 mg/m.sup.2 of a scavenger, 1-octadecyl-4,4-dimethyl-2-[2-hydroxy-5-(N-(7-caprolactamido)sulfonamido]thiazolidine, about 40 mg/m.sup.2 of a magenta filter dye, and about 416 mg/m.sup.2 of gelatin;
11. a yellow filter layer comprising about 390 mg/m.sup.2 of benzidine yellow dye and about 194 mg/m.sup.2 of gelatin;
12. a yellow image dye-providing layer comprising about 1068 mg/m.sup.2 of a yellow image dye-providing material represented by the formula ##STR11## and about 107 mg/m.sup.2 of polyvinyl alcohol and about 427 mg/m.sup.2 of gelatin;
13. about 715 mg/m.sup.2 of the complex of phenyl tertiarybutyl hydroquinone and dimethylterephthalamide, about 50 mg/m.sup.2 of 5-t-butyl-2,3-bis[(1-phenyl-1H-tetrazol-5-yl)thio]-1,4-benzenediol bis[(2-methanesulfonylethyl)carbamate]; and about 319 mg/m.sup.2 of gelatin;
14. a blue-sensitive silver iodobromide layer comprising about 83 mg/m.sup.2 of silver (0.9 microns), about 125 mg/m.sup.2 of silver (1.4 microns), and about 92 mg/m.sup.2 of gelatin;
15. a layer comprising about 450 mg/m.sup.2 of an ultraviolet filter (Tinuvin, from Ciba-Geigy), about 35 mg/m.sup.2 of benzidine yellow dye and about 194 mg/m.sup.2 of gelatin; and
16. a layer comprising about 128 mg/m.sup.2 of silica and about 255 mg/m.sup.2 of gelatin.
Film units were prepared utilizing each of the receiving elements of EXAMPLES III and IV and the above-described photosensitive element. In each case, after photoexposure of the photosensitive element, the image-receiving element and the photosensitive element were arranged in face-to-face relationship, i.e., with their respective supports outermost, and a rupturable container containing an aqueous alkaline processing composition was affixed between the image-receiving and photosensitive elements at the leading edge of each film unit such that the application of compressive pressure to the container would rupture the seal of the container along its marginal edge and distribute the contents uniformly between the respective elements. The composition of the aqueous alkaline processing composition utilized for the processing of each film unit is set forth in TABLE 1.
TABLE 1______________________________________Processing CompositionComponent Parts by Weight______________________________________Potassium hydroxide 5.11-(4-hydroxyphenyl)-1H- 0.004tetrazole-5-thiolN-butyl-.alpha.-picolinium 1.8bromide1-methylimidazole 0.251,2,4-triazole 0.606hypoxanthine 1.033,5-dimethylpyrrazole 0.418sodium hydroxide 1.282-(methylamino)ethanol 0.25Guanine 0.125Aluminum hydroxide hydrate 0.245-amino-1-pentanol 0.5Hydroxyethylcellulose 2.86Chlorobenzenesulfinate 1.0Titanium dioxide 0.17Water Balance to 100______________________________________
Each film unit was subjected to exposure to a standard photographic sensitometric wedge target and was processed at room temperature (about 20.degree. C.) by spreading the processing composition between the image-receiving and photosensitive elements as they were brought into superposed relationship between a pair of pressure rollers having a gap of about 0.0032". After an imbibition period of about 90 seconds, the image-receiving element (photograph) in each case was separated from the remainder of the film unit.
Each of the photographs was evaluated for minimum and maximum reflection densities (Dmin and Dmax, respectively) for red, green and blue, using a densitometer.
The following values, reported in TABLE 2, were obtained.
TABLE 2______________________________________Photographfrom Image-Receiving Dmin DmaxElement R G B R G B______________________________________A 0.12 0.12 0.08 2.20 2.43 2.01B 0.11 0.11 0.07 1.74 2.03 1.78C 0.13 0.14 0.12 1.98 2.22 1.97D 0.12 0.11 0.08 2.18 2.24 1.87E 0.12 0.12 0.09 1.36 1.66 1.55CONTROL 0.11 0.10 0.06 1.75 1.92 1.72______________________________________
EXAMPLE VI
Image-receiving elements prepared in the manner described in EXAMPLE IV so as to replicate Image-Receiving Element A thereof were subjected to photoradiation, prior to their utilization as image-receiving elements in a photographic diffusion transfer process. A photomask was placed over the image-receiving layer of each element to be irradiated, the mask serving to shield the element from the irradiation except in a rectangular target area through which the irradiation passed to effect photoradiation. A hand-held ultraviolet-radiation lamp source (Mineralight.RTM., Model UVGL-25, VVP, Inc.) placed at a distance of two centimeters from the element and providing a fluence of 150 mJ/cm.sup.2 at wavelengths in the range of 250-400 nm was employed. A first element was irradiated for one minute (the element being identified as Image-Receiving Element A-UV1); a second element (Image-Receiving Element A-UV5) was irradiated for five minutes.
Each of Image-Receiving Elements A/UV1 and A/UV5 was utilized for the production of film units, using the photosensitive element and processing composition described in EXAMPLE V. The photosensitive element was photoexposed imagewise through a standardized wedge target and the film unit was processed, all as described in EXAMPLE V. Maximum density measurements were made from the resulting photographs, inside the area of each photograph corresponding to the target area subjected to UV irradiation and outside such area. The measured Dmax values are reported in TABLE 3.
TABLE 3______________________________________Photograph DmaxFrom Image Outside InsideReceiving Target Area Target AreaElement R G B R G B______________________________________A/UV1 2.23 2.37 1.96 2.04 2.04 1.77A/UV5 2.09 2.22 1.88 1.33 1.47 1.44______________________________________
As can be seen from inspection of TABLE 3, subjection of Image-Receiving Element A to ultraviolet irradiation, either for one minute or five minutes, lessened attainable maximum density values (the UV irradiated target areas showing lower values than the non-irradiated areas). Acceptable Dmax values were, however, obtained.
EXAMPLE VII
Image-receiving elements according to the invention were prepared. These were the same as the CONTROL of EXAMPLE III, except that, in lieu of the image-receiving layer thereof, there was substituted in each instance an image-receiving layer as herein specified.
Image-Receiving Element F--an image-receiving layer coated at a coverage of about 300 mg/ft.sup.2 (about 3229 mg/m.sup.2) of a 2:1:0.1 mixture of the 80/20 TMQ/VBT copolymer and polyvinyl alcohol (Airvol 165, Air Products and Chemicals, Inc.).
Image-Receiving Element G--an image-receiving layer coated at a coverage of about 300 mg/ft.sup.2 (about 3229 mg/m.sup.2) of a 2:1:0.1 mixture of the 80/20 TMQ/VBT copolymer and polyvinyl alcohol (Elvatol 9050, E.I. dupont de Nemours).
Image-Receiving Elements F and G were each irradiated through a target with ultraviolet radiation, in the manner described in EXAMPLE VI. Image-Receiving Elements F/UV1 and F/UV5 were subjected to one minute and five minutes irradiation, respectively. Image-Receiving Elements G/UV1 and G/UV5 were subjected to one minute and five minutes irradiation, respectively.
Each of the elements was utilized for the production of film units, using the photosensitive element and processing composition described in EXAMPLE V. The photosensitive element was photoexposed imagewise through a standardized wedge target and the film unit was processed, all as described in EXAMPLE V. Maximum density measurements were made from the photographs, inside the area of each photograph corresponding to the target area subjected to UV irradiation and outside such area. The measured Dmax values are reported in TABLE 4.
TABLE 4______________________________________Photograph DmaxFrom Image Outside UV Inside UVReceiving Target Area Target AreaElement R G B R G B______________________________________F/UV1 2.19 2.29 1.88 2.22 2.30 1.83F/UV5 2.19 2.28 1.82 1.58 1.53 1.41G/UV1 1.92 1.92 1.62 2.17 2.14 1.73G/UV5 1.96 2.01 1.63 1.64 1.65 1.48______________________________________
As can be seen from inspection of TABLE 4, subjection of Image-Receiving Elements F and G to one minute of UV irradiation provided a slight increase in measured Dmax values i.e., greater Dmax in the UV-target areas than in the non-irradiated areas, Five-minute UV irradiation treatments produced, in each case, lower Dmax values than were realized in non-irradiated areas, indicative of a duration of irradiation in excess of optimal irradiation.

Number	Name	Date
4563411	Bronstein-Bonte	Jan 1986
4766052	Nakamura et al.	Aug 1988
4794067	Grasshoff et al.	Dec 1988
5039813	Fazio et al.	Aug 1991

Copolymeric mordants and photographic products and processes containing same

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