US3619155A

US3619155A - Photographic products and processes utilizing a polyvalent metal ion-cross-linked polymeric layer

Info

Publication number: US3619155A
Application number: US42394A
Authority: US
Inventors: Richard W Young
Original assignee: Polaroid Corp
Current assignee: Polaroid Corp
Priority date: 1970-06-01
Filing date: 1970-06-01
Publication date: 1971-11-09
Anticipated expiration: 1988-11-09
Also published as: JPS5344823B1; IT989594B; CA944208A; DE2127144C3; DE2127144A1; NL171842B; NL171842C; FR2095706A6; BE767870R; DE2127144B2; NL7107484A; GB1355133A

Abstract

A photographic film unit adapted to be processed by passing said unit between a pair of juxtaposed pressure-applying members which includes a composite structure composed of a plurality of layers including a photosensitive silver halide emulsion layer having associated therewith a dye image-forming material which is processing composition soluble and diffusible as a function of exposure of the photosensitive silver halide emulsion layer to incident actinic radiation; a polymeric layer dyeable by said dye image-forming material; opacifying means adapted to be interposed intermediate the dyeable polymeric layer and next adjacent silver halide emulsion layer and associated dye image-forming material in a quantity adapted to mask dye image-forming material in a quantity adapted to mask dye image-forming material associated with the silver halide emulsion layer subsequent to photoexposure of the emulsion; a substantially continuous polymeric layer having associated therewith a metal ion; e.g., a metal ion crosslinked polymeric layer, adapted to be interposed intermediate the dyeable polymeric layer and next adjacent silver halide emulsion layer and associated dye image-forming material, subsequent to substantial dye image formation by transfer of dye image-forming material from association with the silver halide emulsion layer to the dyeable polymeric layer and to restrain transfer of dye image-forming material and other products of the development process which effect stability and/or quality of the image; and a rupturable container containing processing composition and adapted to discharge its contents between said dyeable polymeric layer and the photosensitive silver halide emulsion layer.

Description

United States Patent Inventor Richard W. Young Wellesley Hills, Mass.

Appl. No. 42,394

Filed June 1,1970

Patented Nov. 9, 197! Assignee Polaroid Corporation Cambridge, Mass.

Primary ExaminerNorman G. Torchin Assistant Examiner-Alfonso 'I. SuroPico Atromeys-Brown and Mikulka and Philip G. Kiely OPMIUE LA E CVAN DYE DE IED SENSIIIV PER Luca iz s itvm NALiDt tuucslou LAvrR D A E Y I E E DEVELOPER LIVER I N Y GREEN SENQIYIVE SILVER NAL DE EMUEtON LAVER V IXVIILDPEI LAVEl IUJC SENSlYIVE SILVEI NALIDE EHUIJION LAVEN a r AUXILLIRV LAYER r ALKALFJNE PROCESSING COMPOSITION CONYMNINO OHCl VIN IMAGE RECEIVING LAVEN YRANSPIRENY LAVER OPIOUE LAYER CVAN DYE DEVELOPER LAYER NED SENSITIVE SILVER NILID r: vi" E EMULSION LAYER in nu uzvzcneen LAYER IYIV I :rg SILVER mum: EMULSION LAYER Lww rm: acvcmezn LAYER \BLUE srusrnv: Sl v QMLU" My an mum: EMULSION LAYEN 1m: ocvzmrm IMHZRNEABLE new.

\llom POLYMERIC LAVER was: RECEIVING LAYER rnmsmrzur uvzn ABSTRACT: A photographic film unit adapted to be processed by passing said unit between a pair of juxtaposed pressure-applying members which includes a composite structure composed of a plurality of layers including a photosensitive silver halide emulsion layer having associated therewith a dye image-forming material which is processing composition soluble and difi'usible as a function of exposure of the photosensitive silver halide emulsion layer to incident actinic radiation; a polymeric layer dyeable by said dye image-forming material; opacifying means adapted to be interposed intermediate the dyeable polymeric layer and next adjacent silver halide emulsion layer and associated dye image-forming material in a quantity adapted to mask dye image-forming material in a quantity adapted to mask dye image-fonning material associated with the silver halide emulsion layer subsequent to photoexposure of the emulsion; a substantially continuous polymeric layer having associated therewith a metal ion; e.g., a metal ion cross-linked polymeric layer, adapted to be interposed intermediate the dyeable polymeric layer and next adjacent silver halide emulsion layer and associated dye image-forming material, subsequent to substantial dye image formation by transfer of dye image-fonning material from association with the silver halide emulsion layer to the dyeable polymeric layer and to restrain transfer of dye image-forming material and other products of the development process which effect stability and/or quality of the image; and a rupturable container containing processing composition and adapted to discharge its contents between said dyeable polymeric layer and the photosensitive silver halide emulsion layer.

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INVENTOR. RICHARD W. YOUNG PIIO'IOGRAPIIIC PRODUCTS AND PROCESSES UTILIZING A POLYVALENT METAL ION-CROSS- LINKED POLYMERIC LAYER The present invention relates to photography and, more particularly, to photographic products particularly adapted for employment in photographic diffusion transfer color processes.

The primary objects of the present invention are to provide photographic products particularly adapted for employment in diffusion transfer color processes; to provide photographic products which comprise a photosensitive composite structure which contains a plurality of essential layers including a first dimensionally stable, liquid impermeable layer, photosensitive silver halide emulsion layer having a dye image-forming material associated therewith which is soluble and diffusible in processing composition as a function of the point-to-point degree of exposure of its asociated silver halide emulsion layer, a polymeric layer dyeable by the dye image-forming material, and a second dimensionally stable, liquid impermeable layer, transparent to incident radiation, a substantially continuous polymeric layer having metal ions associated therewith adapted to be interposed intermediate the dyeable polymeric layer and next adjacent silver halide emulsion layer subsequent to substantial dye image formation in the dyeable polymeric layer, in combination with a rupturable container retaining a processing composition fixedly positioned and extending transverse a leading edge of the composite photosensitive structure whereby to effect, upon application of compressive pressure, discharge of the processing composition intermediate the dyeable polymeric layer and photosensitive silver halide emulsion layer next adjacent thereto; to provide a diffusion transfer color film unit of the last-identified type including an opacifying agent adapted to be disposed intermediate the dyeable polymeric layer and the photosensitive emulsion next adjacent thereto in a quantity sufficient to mask the dye image-forming material; to provide a diffusion transfer color film unit of the last-identified type possessing the opacifying agent initially present in the processing composition for discharge intermediate the dyeable polymeric layer and the photosensitive silver halide emulsion next adjacent thereto upon application of compressive pressure to the container and distribution of its contents intermediate the layers; and to provide photographic diffusion transfer color processes employing such products.

Other objects of the invention will in part be obvious and will in part appear hereinafter.

The invention accordingly comprises the product possessing the features, properties and the relation of components and the process involving the several steps and the relation and order of one or more of such steps with respect to each of the others which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.

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 wherein:

FIG. 1 is a perspective view of a photographic film unit embodying the invention;

FIGS. 2, 4 and 6 are diagrammatic enlarged cross-sectional views of the film unit of FIG. I, along section line 2-2, illustrating the association of elements during the three illustrated stages of the performance of a diffusion transfer process, for the production of a multicolor transfer image according to the invention, the thickness of the various materials being exaggerated, and wherein FIG. 2 represents an exposure stage, FIG. 4 represents a processing stage and FIG. 6 represents a product of the process;

FIGS. 3, and 7 are diagrammatic, further enlarged crosssectional views of the film unit of FIGS. 2, 4 and 6, along section lines 3--3, 5-5 and 7-7, respectively, further illustrating, in detail, the arrangement of layers comprising the photosensitive laminate during the three illustrated stages of the transfer process; and

FIGS. 8 and 9 illustrate comparative spectral densities between a control and a film unit of the present invention.

As disclosed in US. Pat. No. 2,983,606, issued May 9, 1961, a photosensitive element containing a dye developer, that is, a dye which is a silver halide developing agent, and a silver halide emulsion may be exposed and wetted by a liquid processing composition, for example, by immersion, coating, spraying, flowing, etc., in the dark, and the exposed photosensitive element superposed prior to, during, or after wetting, on a sheetlike support element which may be utilized as an image-receiving element. In a preferred embodiment, the liquid processing composition is applied to the photosensitive element in a substantially uniform layer as the photosensitive element is brought into superposed relationship with the image-receiving layer. The liquid processing composition, positioned intermediate the photosensitive element and the image-receiving layer, permeates the emulsion to initiate development of the latent image contained therein. The dye developer is immobilized or precipitated in exposed areas as a consequence of the development of the latent image. This immobilization is apparently, at least in part, due to a change in the solubility characteristics of the dye developer upon oxidation and especially as regards its solubility in alkaline solutions. It may also be due in part to a tanning effect on the emulsion by oxidized developing agent, and in part to a localized exhaustion of alkali as a result of development. In unexposed and partially exposed areas of the emulsion, the dye developer is unrelated and diffusible and thus provides an imagewise distribution of unoxidized dye developer dissolved in the liquid processing composition, as a function of the point-to-point degree of exposure of the silver halide emul' sion. At least part of this imagewise distribution of unoxidized dye developer is transferred, by imbibition, to a superposed image-receiving layer or element, said transfer substantially excluding oxidized dye developer. The image-receiving element receives a depthwise diffusion, from the developed emulsion, of unoxidized dye developer without appreciably disturbing the imagewise distribution thereof to provide the reversed or positive color image of the developed image. The image-receiving element may contain agents adapted to mordant or otherwise fix the diffused, unoxidized dye developer. The desired positive image is revealed by stripping the imagereceiving layer from the photosensitive element at the end of a suitable imbibition period.

The dye developers, as noted above, are compounds which contain, in the same molecule, both the chromophoric system of a dye and also a silver halide developing function. By a silver halide developing function is meant a grouping adapted to develop exposed silver halide. A preferred silver halide development function is a hydroquinonyl group. Other suitable developing functions include ortho-dihydroxyphenyl and orthoand para-amino substituted hydroxyphenyl groups. In general, the development function includes a benzenoid developing function, that is, an aromatic developing group which forms quinonoid or quinone substances when oxidized. Multicolor images may be obtained using color image-forming components such as, for example, the previously mentioned dye developers, in diffusion transfer processes by several techniques. One such technique contemplates obtain ing multicolor transfer images utilizing dye developers by em ployment of an integral multilayer photosensitive element, such as is disclosed in the aforementioned US. Pat. No. 2,983,606, and particularly with reference to FIG. 9 of the patents drawing wherein at least two selectively sensitized photosensitive strata, superposed on a single support, are processed, simultaneously and without separation, with a single, common imagereceiving layer. A suitable arrangement of this type comprises a support carrying a red-sensitive silver halide emulsion stratum, a green-sensitive silver halide emulsion stratum and a blue-sensitive silver halide emulsion stratum, said emulsions having associated therewith, respectively, for example, a cyan dye developer, a magenta dye developer and a yellow dye developer. The dye developer may be utilized in the silver halide emulsion layer, for example, in the form of particles, or it may be employed as a layer behind the appropriate silver halide emulsion strata. Each set of silver halide emulsion and associated dye developer strata are disclosed to be optionally separated from other sets by suitable interlayers, for example, by a layer of gelatin or polyvinyl alcohol. In certain instances, it may be desirable to incorporate a yellow filter in front of the green-sensitive emulsion and such yellow filter may be incorporated in an interlayer. However, where desirable, a yellow dye developer of the appropriate spectral characteristics and present in a state capable of func tioning as a yellow filter may be employed. In such instances, a separate yellow filter may be omitted.

The dye developers are preferably selected for their ability to provide colors that are useful in carrying out subtractive color photography, that is, the previously mentioned cyan, magenta and yellow. The dye developers employed may be incorporated in the respective silver halide emulsion or, in the preferred embodiment, in a separate layer behind the respective silver halide emulsion. Specifically, the dye developer may, for example, be in a coating or layer behind the respective silver halide emulsion and such a layer of dye developer may be applied by use of a coating solution containing about 0.5 to 8 percent, by weight, of the respective dye developer distributed in a film-forming natural, or synthetic, polymer, for example, gelatin, polyvinylalcohol, and the like, adapted to be permeated by the chosen diffusion transfer fluid processing composition.

As examples of materials, for use as the image-receiving layer, mention may be made of solution dyeable polymers such as nylon as, for example, N-methoxymethyl polyhexamethylene adipamide; partially hydrolyzed polyvinyl acetate; polyvinyl alcohol with or without plasticizers; cellulose acetate with filler as, for example, one-half cellulose acetate and one-half oleic acid; gelatin; and other materials of a similar nature. Preferred materials comprise polyvinyl alcohol or gelatin containing a dye mordant such as poly-4-vinylpyridine, as disclosed in US. Pat. No. 3,148,061, issued Sept. 8, 1964.

As disclosed in the previously cited patents, the liquid processing composition referred to for effecting multicolor diffusion transfer processes comprises an aqueous solution of an alkaline material, for example, diethylamine, sodium hydroxide or sodium carbonate and the like, and preferably possessing a pH in excess of 12, and most preferably includes a viscosity-increasing compound constituting a film-fonning material of the type which, when the composition is spread and dried, forms a relatively firm and relatively stable film. The film-forming materials disclosed comprise high molecular weight polymers such as polymeric, water-soluble ethers which are inert to an alkaline solution such as, for example, a hydroxyethyl cellulose or sodium carboxymethyl cellulose. Additionally, film-forming materials or thickening agents whose ability to increase viscosity is substantially unaffected if left in solution for a long period of time are also disclosed to be capable of utilization. As stated, the film-forming material is preferably contained in the processing composition in such suitable quantities as to impart to the composition a viscosity in excess of I cps. at a temperature of approximately 24 C. and preferably in the order of 100,000 cps. to 200,000 cps. at that temperature.

In accordance with aforementioned US. Pat. No. 2,983,606, an image-receiving layer of the type disclosed in that patent need not be separated from its superposed contact with the photosensitive element, subsequent to transfer image formation, if the image-receiving element is transparent and a processing composition containing a substance rendering the processing composition layer opaque is spread between the image-receiving layer and the silver halide emulsion or emulsrons.

However, it has been found, if the image-receiving element is maintained in contact with the photosensitive element, subsequent to dye developer transfer image formation, and includes the presence of an alkaline processing composition,

necessarily having a pH at which dye developer, for example, in reduced form, diffuses to form the dye transfer image, intermediate the elements, the transfer image thus formed is unstable over an extended period of time. The dye image instability is due, at least in part of the presence of what is, in general, a relatively high pH alkaline composition in intimate contact with the dye or dyes forming the image. This contact itself provides instability to the molecular structure of dye by, for example, catalyzing degradation and undesirable structural shifts effecting the spectral absorption characteristics of the image dye. In addition, the presence of an alkaline composition, possessing a pH at which the dye, for example, in reduced form, diffuses, also provides an integral dynamic system wherein oxidized dye, immobilized in areas of the photosensitive element, as a function of its development, with the passage of time attempts to generate, in such areas, an equilibrium between oxidized and reduced dye. in that the pH of the dynamic system is such that diffusion of the reduced form of the dye will occur, such reduced dye will, at least in part, transfer to the image-receiving layer and the resultant diffusion will imbalance the equilibrium, in such areas of the photosensitive element, in favor of additional formation of reduced dye. As a function of the efficiency of the imagereceiving layer, as a dye sink, such nonimagewise dyeing of the image-carrying layer still further imbalances the equilibrium in favor of the additional formation of dye in reduced, diffusible form. Under such circumstances, the transfer image definition, originally carried by the image-receiving layer, will suffer a continuous decrease in the delta between the image's maximum and minimum densities and may, ultimately, result in the image-receiving element's loss of all semblance of image definition; merely becoming a polymeric stratum carrying a relatively uniform overall dyeing.

The problems inherent in fabricating a film unit of the type wherein the image-receiving element, the alkaline processing composition and the photosensitive element are maintained in contiguous contact subsequent to dye transfer image formation, for example, a film unit of the type described hereinbefore with reference to aforementioned US. Pat. No. 2,983,606, may be effectively obviated by fabrication of a film unit in accordance with the physical parameters specifically set forth in copending U.S. Pat. Nos. 3,415,644; 3,415,645; and 3,415,646, issued Dec. 10, 1969, respectively, in the name of Edwin H. Land.

Specifically an integral photographic film unit particularly adapted for the production of a dye transfer image of unexpectedly improved stability and other properties, by a color diffusion transfer process will be constructed, for example, in accordance with aforementioned US. Pat. No. 3,415,644, to include a photosensitive element comprising a laminate having, in sequence, as essential layers, a dimensionally stable opaque layer; a photosensitive silver halide emulsion layer having associated therewith dye image-providing material which is soluble and diffusible, in alkali, at a first pH; an alkaline solution permeable polymeric layer dyeable by the dye image-providing material; a polymeric acid layer containing sufficient acidifying groups to effect reduction, subsequent to substantial transfer dye image formation, of a selected processing solution having the first pH to a second pH at which said dye image-providing material is insoluble and nondiffusible; and a dimensionally stable transparent layer. In combination with the laminate, a rupturable container retaining an aqueous alkaline processing composition having the first pH and containing an opacifying agent, in a quantity sufficient to mask the dye image-providing material, is fixedly positioned and extends transverse a leading edge of the laminate whereby to effect unidirectional discharge of the containers contents between the alkaline solution permeable and dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto, upon application of compressive force to the container.

It will also be recognized that the dimensionally stable polymeric support layer next adjacent the photosensitive silver halide emulsion layer or layers may be transparent, as disclosed in aforementioned U.S. Pat. No, 3,415,646, and that in such instance the opacifying agent may be initially dispersed in the composite film unit intermediate the dyeable polymeric layer and the silver halide emulsion layer next ad'- jacent, as disclosed in aforementioned U.S. Pat. No. 3,415,645.

Employment of the last-mentioned film units, according to the described color diffusion transfer photographic process, specifically provides for the production of a highly stable color transfer image accomplished, at least in part, by effectively obviating the previously discussed disadvantages of the prior art products and processes, by in process adjustment of the environmental pH of the film unit from a pH at which transfer processing is operative to a pH at which dye transfer is inoperative subsequent to substantial transfer image formation. The stable color transfer image is obtained irrespective of the fact that the film unit is maintained as an integral laminate unit during exposure, processing, viewing, and storage of the unit, which transfer image exhibits the required maximum and minimum dye transfer image densities, dye saturation, hues and definition.

However, film units fabricated in accordance with the parameters set forth above specifically require the presence of the stated neutralizing component to effect in situ process adjustment of the film units operational pH range.

Specifically, the film units require the presence of a polymeric neutralizing layer such as, for example, of the type set forth in US. Pat. No. 3,362,819 which, most preferably, includes the presence of an inert timing or spacer layer intermediate the polymeric layer carried on a support and the image-receiving layer.

As set forth in the last-mentioned patent, the polymeric neutralizing layer may comprise polymers which contain acid groups, such as carboxylic acid and sulfonic acid groups, where are capable of forming salts with alkali metals, such as sodium, potassium etc., or with organic bases, particularly quaternary ammonium bases, such as tetramethyl ammonium hydroxide, or potentially acid-yielding groups, such as anhydrides or lactones, or other groups which are capable of reacting with bases to capture and retain them. The acidreacting group is, of course, nondiffusible from the acid polymer layer. in the preferred embodiments disclosed, the acid polymer contains free carboxyl groups and the transfer processing composition employed contains a large concentration of sodium and/or potassium ions. The acid polymers stated to be most useful are characterized by containing free carboxyl groups, being insoluble in water in the free acid form, and by forming water-soluble sodium and/or potassium salts. One may also employ polymers containing carboxylic acid anhydride groups, at least some of which preferably have been converted to free carboxyl groups prior to imbibition. While the most readily available polymeric acids are derivatives of cellulose or of vinyl polymers, polymeric acids from other classes of polymers may be used. As examples of specific polymeric acids set forth in the application, mention may be made of dibasic acid half-ester derivatives of cellulose which derivatives contain free carboxyl groups, e.g., cellulose acetate hydrogen phthalate, cellulose acetate hydrogen glutarate, cellulose acetate hydrogen succinate, ethyl cellulose hydrogen succinate, ethyl cellulose acetate hydrogen succinate, cellulose acetate hydrogen succinate hydrogen phthalate; ether and ester derivatives or cellulose modified with sulfoanhydrides, e.g., with ortho-sulfobenzoic anhydride; polystyrene sulfonic acid; carboxymethyl cellulose; polyvinyl hydrogen phthalate; polyvinyl acetate hydrogen phthalate; polyacrylic acid; acetals of polyvinyl alcohol with carboxy or sulfo substituted aldehydes, e.g., o-, m-, or p-benzaldehyde sulfonic acid or carboxylic acid; partial esters of ethylene/maleic anhydride copolymers; partial esters of methyl-vinyl ether/maleic anhydride copolymers; etc.

As previously noted, the pH of the processing composition preferably is of the order of at least 12 to 14. The acid layer is disclosed to contain at least sufficient acid groups to effect a reduction in the pH of the image layer from a pH of about 12 to 14 to a pH of at least 11 or lower at the end of the imbibition period, and preferably to a pH of about 5 to 8 within a short time after imbibition, thus requiring, of course, that the action of the acid be accurately so controlled as not to interfere with either development of the negative or image transfer of unoxidized dye developers. For this reason, the pH of the image layer must be kept at a functional transfer level, for example, l2 to 14 until the dye image has been formed after which the pH is reduced very rapidly to a pH below that at which dye transfer may be accomplished, for example, at least about 11 and preferably about pH 9 to 10. Unoxidized dye developers containing hydroquinonyl developing radicals diffuse from the negative to the positive as the sodium or other alkali salt. The difi'usion rate of such dye image-forming components thus is at least partly a function of the alkali concentration, and it is necessary that the pH of the image layer remain on the order of, for example, 12 to 14 until transfer of the necessary quantity of dye has been accomplished. The subsequent pH reduction, in addition to its desirable effect upon image light stability, serves a highly valuable photographic function by substantially terminating further dye transfer.

In order to prevent premature pH reduction during transfer processing, as evidenced, for example, by an undesired reduction in positive image density, the acid groups are disclosed to be so distributed in the acid polymer layer that the rate of their availability to the alkali is controllable, e.g., as a function of the rate of swelling of the polymer layer which rate in turn has a direct relationship to the diffusion rate of the alkali ions. The desired distribution of the acid groups in the acid polymer layer may be effected by mixing the acid polymer with a polymer free of acid groups, or lower in concentration of acid groups, and compatible therewith, or by using only the acid polymer but selecting one having a relatively lower proportion of acid groups. These embodiments are illustrated, respectively, in the cited copending application, by (a) a mixture of cellulose acetate and cellulose acetate hydrogen phthalate and (b) a cellulose acetate hydrogen phthalate polymer having a much lower percentage of phthalyl groups than the firstmentioned cellulose acetate hydrogen phthalate.

It is also there disclosed that the layer containing the polymeric acid may contain a water-insoluble polymer, preferably a cellulose ester, which acts to control or modulate the rate at which the alkali salt of the polymer acid is formed. As examples of cellulose esters contemplated for use, mention is made of cellulose acetate, cellulose acetate butyrate, etc. The particular polymers and combinations of polymers employed in any given embodiment are, of course, selected so as to have adequate wet and dry strength and when necessary or desirable, suitable subcoats are employed to help the various polymeric layers adhere to each other during storage and use.

The inert spacer layer of the last-mentioned patent, for example, an inert spacer layer comprising polyvinyl alcohol or gelatin, acts to time control the pH reduction by the polymeric acid layer. This timing is disclosed to be a function of the rate at which the alkali diffuses through the inert spacer layer. It is there stated to have been found that the pH does not drop until the alkali has passed through the spacer layer, i.e., the pH is not reduced to any significant extent by the mere diffusion into the interlayer, but the pH drops quite rapidly once the alkali difiuses through the spacer layer.

It has now been quite unexpectedly discovered that the problems inherent in fabricating a film unit of the type where the image-receiving element, the alkali processing composition and the photosensitive element are maintained in contiguous contact during processing and subsequent to dye transfer image formation, for example, a film unit of the type described, with reference to aforementioned US. Pat. No. 2,983,606, may be effectively obviated in a considerably simplified manner by fabrication of a film unit in accordance with the physical parameters detailed below.

Specifically, it has been quite unexpectedly discovered that an integral photographic film unit of simplified construction and particularly adapted for the production of dye transfer images of unexpectedly improved stability and other desirable properties by a color diffusion transfer process will be constructed to include a photosensitive element comprising a composite structure possessing, in sequence, as essential layers, a first dimensionally stable layer, a photosensitive silver halide emulsion layer having associated therewith a dye image-fonning material which is soluble and diffusible as a function of the point-to-point degree of emulsion photoexposure, a polymeric layer dyeable by the dye image-forming material, and a second dimensionally stable layer transparent to incident actinic radiation. In combination with the composite structure, a rupturable container retaining a processing composition is fixedly positioned and extends transverse a leading edge of the composite structure whereby to effect, upon application of compressive pressure, discharge of the processing composition intermediate the dyeable polymeric layer and the photosensitive silver halide emulsion and associated dye image-forming material next adjacent thereto. in addition, the aforementioned integral photographic film unit possesses means for interposing between said dyeable polymeric layer and the photosensitive silver halide emulsion next adjacent thereto, a continuous, polymeric layer having metal ions associated therewith, after substantial image formation has been accomplished in said dyeable polymeric layer, in order to obviate further migration of dye or reaction products or residues of the photographic development process which are detrimental to quality and/or stability of dye transfer images.

Means for providing said continuous polymeric layer include disposing a substantially continuous polymeric material intermediate the dye image-forming layer and the photosensitive silver halide emulsion next adjacent thereto, said polymeric material being normally permeable to the dye image-forming material, but when associated with a metal ion provided by, for example, a metallic salt disposed in the film unit, functions to prevent further transfer of dye image-forming material or other reaction products or residues, after the dye image-forming material has completed imagewise transfer, which effect image quality by, e.g., causing stain or darkening in the image highlights or indiscriminate dye imageforrning material transfer.

The metal ion and polymeric material may be selected to provide, upon association, a metal ion cross-linked polymeric material substantially impermeable to at least dye image-fenning material.

Means for the formation of such a continuous polymeric layer specifically include, for example, providing a film-forming polymeric processing composition component such as a viscosity increasing agent and metal ion which may be directly or by means of a metal ion donor located at various positions in the photographic film unit such that after a predetermined time following the distribution of the processing composition, the metal ion component will become functionally associated with the polymeric material whereupon a barrier to the unwanted dye image-forming materials and process reaction products is formed, intermediate the dyeable polymeric layer and the next adjacent photosensitive silver halide emulsion.

in an alternative embodiment, a normally dye image-forming material penneable polymeric layer is located as a preformed layer intermediate the dyeable polymeric layer and next adjacent photosensitive silver halide emulsion layer and a diffusible metal ion contacts with the polymeric layer preventing the transfer to the dyeable polymeric layer of undesirable materials.

Thus, in situ barrier formation of the present invention may be provided by initially disposing a polymeric material permeable to the dye image-forming material intermediate the dyeable polymeric layer and the next adjacent photosensitive silver halide emulsion and a metal ion donor in an element of the composite film unit and/or incorporated in the processing composition to provide during processing, subsequent to substantial dye transfer image formation, association with the polymeric material in a concentration effective to provide a barrier substantially impermeable to further dye image-forming material transfer.

While the prevention of transfer of unwanted material to the dyeable polymeric layer has been characterized as a barrier, the operative mechanism which may be involved is not in all circumstances fully known and understood, and in fact may not in all instances involve the formation of a strictly speaking physical barrier. Thus, while many of the metal ions are known to cross-link the polymers employed, some may not under the conditions extant in the film unit but still the abovementioned undesired transfer is substantially prevented. Subsequent to substantial dye image-forming material transfer to the dyeable layer it is necessary to prevent further transfer of excess or unwanted dye image-forming material. In addition, the residue of the photographic processing reagents such as booster developer, onium compounds, etc., and the reaction products thereof, which may result in the formation of colored forms, must also be restrained from passing to the dyeable polymeric layer. Thus, it has been unexpectedly found that such unwanted materials, diverse in chemical constitution and molecular configuration, can be restrained by chemical and/or physical means from transferring to the dyeable polymeric layer, by employing, with a film-forming polymeric material which is normally permeable to said materials, an associated metal ion.

The metal ion may be disposed, for example, as a metallic salt, in the processing composition; in permeable layers adjacent to the photosensitive silver halide emulsion layers; in permeable layers adjacent the dyeable polymeric layer; in the photosensitive silver halide emulsion layers or in the dyeable polymeric layer, or the like. Thus, the specific time delay from the start of dye image-forming material transfer until the permeability of the polymeric material is decreased to such a degree that the dye image-forming material is incapable of passing therethrough is determined by the predetermined time necessary for the metal ion to diffuse into contact with the polymeric material and/or by employing a pH-controlled system wherein the metal ion will not be functionally available at a preselected first pH, but as the pH of the system is converted during processing to a preselected second pH, effective metal ion contact is generated and the modulation-of the system increases to a point where the dye image-fonning material and other unwanted materials are incapable of deleterious transfer to the dyeable polymeric layer.

in a particularly preferred embodiment, the barrier is formed by employing a film-fonning polymeric component, for example, a viscosity-increasing component, of the processing composition to provide the requisite polymeric layer in situ during processing of the film unit. As indicated above, carboxymethyl hydroxyethyl cellulose and carboxymethyl cellulose are commonly employed as viscosity-increasing agents in difiusion transfer processes as more fully disclosed and discussed in numerous of the aforementioned patents and particularly in US. Pat. No. 2,983,606. In employing such preferred polymers, the metal ion, for example, derived from a processing composition ionizable metallic salt donor, may be disposed in the various above-indicated locations conveniently since the metal ion and the specified polymers are stable and nonreactive to each other in each other's absence and/or while the pH of the system comprises a preselected insulating environment and the barrier formation mechanism occurs at preselected pH generated during processing of the film unit.

To avoid excessive and premature consumption of the alkaline material upon processing composition-metal ion contact with the concurrent formation of insoluble metal hydroxides and pH lowering, excess alkaline material may be provided to the processing composition to minimize or obviate the effect of such initial pH lowering.

it should be understood that the present invention contemplates the employment of combinations of metal ions as well as a single metal ion and combinations of polymers. Thus, the most favorable properties of each of the materials can be employed in a film structure to achieve the greatest degree of efficiency in barrier formation and to tailor the speed and manner of ban'ier formation as well as the type and location of barrier formed. For example, in one embodiment, cadmium acetate is initially disposed in the dyeable polymeric layer and nickel ion is disposed in the processing composition as nickel carbonate with carboxymethyl cellulose. When the pH of the system drops from an initial first pH to a second pH the cadmium and nickel cations become available to the system, thus forming the barrier to the transfer of dye image-forming materials and other undesirable materials to the dyeable polymer.

As examples of suitable cations for use in the practice of the present invention, mention may be made of polyvalent metal cations, such as cadmium, calcium, magnesium, zinc, barium and nickel, preferably trivalent and tetravalent metal cations such as zirconium, aluminum and chromium. The more preferred cations are those with the higher valence. The particular anion selected where one or more metallic salts are utilized is not critical; it is only required that the salt be soluble in the processing composition to produce the required metal ion species under the desired pH conditions and be compatible with the particular environment in which it is disposed in the composite film structure and be photographically acceptable, that is, produce no deleterious effects on the photographic capability of the film unit. Preferred anions include the acetate, nitrate and carbonate. The specific salt selected, or alternatively, chelated metal cation, as indicated above, will be determined by the operator depending upon the location of the salt in the film unit, as well as the desired time and location of the barrier formation.

In addition to the aforementioned carboxymethyl cellulose and carboxy hydroxyethyl cellulose, other suitable polymers which may fomi the desired barrier to the dye image-forming material and processing reagents include hydroxyethyl cellulose, polyacrylic acid, polyvinyl alcohol, and polymethacrylic acid as well as other film-forming polymers known to the art which possess free carboxyl, hydroxyl, amino or mercapto groups. It should be understood that the particular metal ion and polymer will be selected with regard to photographic suitability and compatibility with the other components in the film unit. In a particularly preferred embodiment, the filmfonning polymeric layer is composed of approximately 90 percent carboxymethyl cellulose and percent hydroxyethyl cellulose and the metal ion is zirconium.

ln embodiments of the present invention predicated upon migration of a metal ion to render, for example, a cast layer impermeable to image-forming materials, it may be desirable to incorporate in such embodiments mechanisms particularly designed to inhibit migration of such metal ion, e.g., diffusion delay layers, etc., until image formation has gone to substantial completion. Such techniques are well known in diffusion transfer photographic technology. As stated above, if the dynamics of a particular system are appropriate, the metal ion may be incorporated in the processing composition. Furthermore, in embodiments of the present invention directed toward cross-linking a precast layer of polymeric material not cast from the processing composition, it is preferred that such layer be located intermediate the dyeable layer and the silver halide emulsion layer next adjacent thereto at a position more distal from the image-receptive layer than the processing composition is to occupy.

in general, the amount of polymeric materials and metal ion utilized to form the herein denoted barrier layers will be determined empirically since various materials will provided different barrier effects for given concentrations. It has been found that, as a rule, a sufficient concentration of polymeric material to provide a continuous layer possessing a thickness of approximately 20 microns will suffice to provide the designated functionality to the system. Upon formation of the ultimate film the substantially continuous layer may contain entrained or entrapped therein one or more of the components, adjuvants or agents originally retained by the processing composition or the like, such as opacifying agent initially distributed in the processing composition in the preferred film unit embodiments detailed hereinabove.

As stated above, the substantially continuous polymeric film provided within one or more of the embodiments denoted herein, in addition to being impermeable to excess solubilized dye image-forming materials will also be substantially impenneable to solubilized photographic adjuncts present in the film unit in general and more particularly those possessing physical dimensions as, for example, molecular size, less than that of dye developer such as, for example, antifoggants, development restrainers, quaternary accelerators, emulsion stabilizers and sensitizers and the like, and reaction products thereof, in order to still further enhance maintenance of dye transfer image stability and acuity.

Although both dimensionally stable layers may be transparent and in such instance, an opacifying agent may be initially dispersed intermediate the dyeable polymeric layer and the next adjacent silver halide emulsion layer, in a quantity sufficient to mask the dye image-forming material, such opacifying agent will preferably be disposed within the processing composition, in a quantity sufficient to mask the dye imageforming material upon distribution of the processing composition intermediate the last-stated layers, and, most preferably, the dimensionally stable layer next adjacent the photosensitive silver halide emulsion layer will be opaque with respect to externally derived incident actinic radiation.

ln view of the fact that the preferred dye image-providing materials comprise dyes which are silver halide developing agents, as stated above, for purposes of simplicity and clarity, the present invention is described hereinafter in terms of such dyes, without limitation of the invention to the illustrative dyes denoted, and, in addition, the photographic film unit structure will be detailed hereinafter employing the last-mentioned preferred structural embodiment, without limitation of the invention to the preferred structure denoted.

In a preferred embodiment of the present invention, the film unit is specifically adapted to provide for the production of a multicolor dye transfer image and the photosensitive laminate comprises, in orderof essential layers, the dimensionally stable opaque layer; at least two selectively sensitized silver halide emulsion strata each having dye image-providing materials of predetermined color associated therewith which are soluble and difi'usible in alkaline processing composition as a function of the point-to-point degree of exposure of the respective associated silver halide emulsion strata; an alkaline solution permeable polymeric layer dyeable by the dye imageproviding materials; and the dimensionally stable transparent layer.

The silver halide emulsions comprising the multicolor photosensitive laminate preferably possess predominant spectral sensitivity to separate regions of the spectrum and each has associated therewith a dye, which is a silver halide developing agent and is, most preferably, substantially soluble in the reduced form only at a selected pH posseming sub- I sequent to processing a spectral absorption range substantially complementary to the predominant sensitivity range of its associated emulsion.

In the preferred embodiment, each of the emulsion strata, and its associated dye, is separated from the remaining emulsion strata, and their associated dye, by separate alkaline solution permeable polymeric interlayers.

In such preferred embodiments of the invention, the silver halide emulsion comprises photosensitive silver halide dispersed in gelatin and is about 0.6 to 6 microns in thickness; the dye itself is dispersed in an aqueous alkaline solution polymeric binder, preferably gelatin, as a separate layer about 1 to 7 microns in thickness; the alkaline solution permeable polymeric interlayers, preferably gelatin, are about 1 to 5 microns in thickness; the alkaline solution dyeable polymeric layer is transparent and about 0.25 to 0.4 mil. in thickness; and each of the dimensionally stable opaque and transparent layers are alkaline solution impermeable and about 2 to 6 mils. in thickness. It will be specifically recognized that the relative dimensions recited above may be appropriately modified, in accordance with the desires of the operator, with respect to the specific product to be ultimately prepared.

In the preferred embodiment of the present inventions film unit for the production of a multicolor transfer image, the respective silver halide/dye developer units of the photosensitive element will be in the form of a tripack configuration which will ordinarily comprise a cyan dye developer/red-sensitive emulsion unit contiguous the dimensionally stable opaque layer, the yellow dye developer/blue-sensitive emulsion unit most distant from the opaque layer and the magenta dye developer/green-sensitive emulsion unit intermediate those units, recognizing that the relative order of such units may be varied in accordance with the desires of the operator.

Reference is now made to FIGS. 1 through 7 of the drawings wherein there is illustrated a preferred film unit of the present invention and wherein like numbers, appearing in the various figures, refer to like components.

As illustrated in the drawings, FIG. 1 sets forth a perspective view of the film unit, designated 10, and each of FIGS. 2 through 7 illustrate diagrammatic cross-sectional views of film unit 10, along the stated section lines 2--2, 33, 5-5 and 7-7, during the various depicted stages in the performance of a photographic diffusion transfer process as detailed hereinafter.

Film unit 10 comprises rupturable container 11, retaining, prior to processing, aqueous alkaline solution 12, and photosensitive laminate 13 including, in order, dimensionally stable opaque layer 14, preferably an actinic radiation-opaque flexible sheet material; cyan dye developer layer 15; red-sensitive silver halide emulsion layer 16; interlayer 17; magenta dye developer layer 18; green-sensitive silver halide emulsion later 19; interlayer 20; yellow dye developer layer 21; blue-sensitive silver halide emulsion layer 22; auxiliary layer 23, which may contain an auxiliary silver halide developing agent; imagereceiving layer 24; and dimensionally stable transparent layer 27, preferably an actinic radiation transmissive flexible sheet material.

The structural integrity of laminate 13 may be maintained, at least in part, by the adhesive capacity exhibited between the various layers comprising the laminate at their opposed surfaces. However, the adhesive capacity exhibited at an interface intermediate image-receiving layer 24 and the silver halide emulsion layer next adjacent thereto, for example, intermediate image-receiving layer 24 and auxiliary layer 23 as illustrated in FIGS. 2 through 7, should be less than that exhibited at the interface between the opposed surfaces of the remainder of the layers forming the laminate, in order to facilitate distribution of processing solution 12 intermediate the stated image-receiving layer 24 and the silver halide emulsion layer next adjacent thereto. The laminates structural integrity may also be enhanced or provided, in whole or in part, by providing a binding member extending around, for example, the edges of laminate l3, and maintainingthe layers comprising the laminate intact, except at the interface between

layers

23 and 24 during distribution of alkaline solution 12 intermediate those layers. As illustrated in the figures, the binding member may comprise a pressure-sensitive tape 28 securing and or maintaining the layers of laminate 13 together at its respective edges. Tape 28 will also act to maintain processing solution 12 intermediate image-receiving layer 24 and the silver halide emulsion layer next adjacent hereto, upon application of compressive pressure to pod l1 and distribution of its contents intermediate the stated layers. Under such circumstances, binder tape 28 will act to prevent leakage of fluid processing composition from the film unit's laminate during and subsequent to photographic processing.

Rupturable container ill may be of the type shown and described in any of U.S. Pat. Nos. 2,543,18l; 2,634,886; 2,653,732; 2,723,051; 3,056,492; 3,056,49l; 3,l52,5l5; and the like. In general, such containers will comprise a rectangular blank of fluidand air-impervious sheet material folded longitudinally upon itself to form two walls 29 which are sealed to one another along their longitudinal and end margins to form a cavity in which processing solution 12 is retained. The longitudinal marginal seal 30 is made weaker than the end seals 31 so as to become unsealed in response to the hydraulic pressure generated within the fluid contents 12 of the container by the application of compressive pressure to walls 29 of the container.

As illustrated in FIGS. 1, 2 and 4, container 1! is fixedly positioned and extends transverse a leading edge of photosensitive laminate 13 whereby to effect unidirectional discharge of the containers contents 112 between image-receiving layer 24 and the stated layer next adjacent thereto, upon application of compressive force to container 11. Thus, container 11, as illustrated in FIG. 2, is fixedly positioned and extends transverse a leading edge of laminate 13 with its longitudinal marginal seal 30 directed toward the interface between imagereceiving layer 24 and auxiliary layer 23. As shown in FIGS. 1, 2 and 4, container 11 is fixedly secured to laminate 13 by extension 32 of tape 28 extending over a portion of one wall 29 of the container, in combination with a separate retaining member such as illustrated retaining tape 33 extending over a portion of the other wall 29 of the container and a portion of laminate 13's surface generally equal in area to about that covered by tape 28.

As illustrated in FIG. 6, extension flap 32 of tape 28 is preferably of such area and dimensions that upon, for example, manual separation of container 11 and tape 33, sub sequent to distribution of processing composition 12, from the remainder of film unit 10, flap 32 may be folded over the edge of laminate 13, previously covered by tape 33, in order to facilitate maintenance of the laminate's structural integrity, for example, during the flexations inevitable in storage and use of the processed film unit, and to provide a suitable mask or frame, for viewing of the transfer image through the picture viewing area of transparent layer 27.

The fluid contents of the container comprise an aqueous alkaline solution, having a pH and solvent concentration at which the dye developers are soluble and diffusible, which contains an opacifying agent in a quantity sufficient to mask the dye developers associated with the silver halide emulsions subsequent to processing and optionally contains a polymeric material adapted upon contact with a metal ion cross-linking agent therefor to provide a substantially continuous, dye impermeable polymeric layer.

In general, in a preferred embodiment the concentration of opacifying agent or agents selected will be that sufficient to prevent further exposure of the film unit's silver halide emulsion or emulsions, by actinic radiation transversing through the dimensionally stable transparent layer, subsequent to distribution of the processing solution intennediate the dyeable polymeric layer and the stated layer next adjacent thereto. Accordingly, the film unit may be processed, subsequent to distribution of the composition, in the presence of such radiation, in view of the fact that the silver halide emulsion or emulsions of the laminate are appropriately protected by incident radiation, at one major surface by the opaque processing composition and at the remaining major surface by the dimensionally stable opaque layer. If the illustrated binder tapes are also opaque, edge leakage of actinic radiation incident on the emulsion or emulsions will also be prevented. The selected opacifying agent, however, should beone providing a background suitable for viewing the dye developer transfer image formed in the dyeable polymeric layer. In general, while substantially any opacifying agent may be employed, it is preferred that an opacifying agent be selected that will not in terfere with the color integrity of the dye transfer image, as viewed by the observer, and, most preferably, an agent which is aesthetically pleasing to the viewer and does not provide a background noise signal degrading, or detracting from, the information content of the image. Particularly desirable opacifying agents will be those providing a white background, for viewing the transfer image, and specifically those conventionally employed to provide background for reflection photographic prints and, especially, those agents possessing the optical properties desired for reflection of incident radiation.

As examples of opacifying agents, mention may be made of barium sulfate, zinc oxide, titanium oxide, barium stearate, silver flake, silicates, alumina, zirconium oxide, zirconium acetyl acetate, sodium zirconium sulfate, kaoline, mica, and the like.

A particularly preferred agent comprises titanium dioxide due to its highly effective reflection properties. In general, based upon percent titanium dioxide (weight volume), a processing composition containing about 40-70 grams of titanium dioxide dispersed in 100 cc. of water will provide a percent reflectance of about 85-90 percent. In the most preferred embodiments, the percent reflectance particularly desired will be in the order of above 85 percent.

Where it is desired to increase the radiation filtering capacity of a processing composition containing, for example, titanium dioxide or the like, selected predominantly for its radiation reflecting properties, beyond that ordinarily obtained or required to obscure or mask the dye and/or developed silver associated with the photosensitive silver halide emulsion layers, it may also be desirable to provide an additional opacifying agent, exhibiting more effective filtration of radiation incident on the transparent support layer during processing, such as carbon black, for example, added in a concentration of about one part carbon black to 100 to 500 parts titanium dioxide, in order to further protect the emulsions from physical fog formation during processing.

In the performance of a diffusion transfer multicolor process employing film unit 10, the unit is exposed to radiation, actinic to photosensitive laminate l3, incident on the laminate's exposure surface 34, as illustrated in FIG. 2.

Subsequent to exposure, as illustrated by FIGS. 2 and 4, film unit is processed by being passed through opposed suitable gapped rolls 35 in order to apply compressive pressure to frangible container 11 and to effect rupture of longitudinal seal 30 and distribution of alkaline processing composition 12, having a pH and solvent concentration at which the cyan, magenta and yellow dye developers are soluble and diffusible and containing film-forming polymer in a concentration suffrcient to provide substantially continuous polymeric layer subsequent to distribution, intermediate dyeable polymeric layer 24 and auxiliary layer 23.

Alkaline processing solution 12 permeates emulsion layers l6, l9 and 22 to initiate development of the latent images contained in the respective emulsions. The cyan, magenta and yellow dye developers, of layers l5, l8 and 21, are immobilized, as a function of the development of their respective associated silver halide emulsions, preferably substantially as a result of their conversion from the reduced form to their relatively insoluble and nondiffusible oxidized form, thereby providing imagewise distributions of mobile, soluble and difiusible cyan, magenta and yellow dye developer, as a function of the pointto-point degree of their associated emulsions exposure. At least part of the imagewise distributions of mobile cyan, magenta and yellow dye developer transfers, by diffusion, to aqueous alkaline solution permeable polymeric layer 24 to provide a multicolor dye transfer image to that layer. Subsequent to substantial transfer image formation, a sufficient portion of a metallic salt, contained, for example, in imagercceiving layer 24, is solubilized by contact with alkaline solution 12 whereby the metal cation of the metallic salt diffuses into contact with the polymeric layer provided as a function of distribution of processing solution 12, intermediate dyeable polymeric layer 24 and auxiliary layer 25, which is normally permeable to dye developer, providing thereby a substantially continuous dye developer impermeable polymeric layer 25 to provide thereby a stable multicolor dye transfer image.

Subsequent to distribution of processing solution 12, container lll may be manually dissociated from the remainder of the film unit, as described above, to provide the product illustrated in FIG. 6.

The present invention will be further illustrated and detailed in conjunction with the following illustrative constructions which set out representative embodiments and photographic utilization of the novel photographic film units of this invention, which however, are not limited to the details therein set forth and are intended to be illustrative only.

Film units similar to that shown in the drawings may be prepared, for example, by coating, in succession, on a gelatin subbed, 4-mile opaque polyethylene terephthalate film base, the following layers:

1. a layer of cyan dye developer l,4-bis-(fi-[hydroquinonyla-rnethyl]-ethylamino)-5,8-dihydroxy-anthraquinone dispersed in gelatin and coated at a coverage of about 150 mgs./ft. of dye and about 200 mgs./ft. of gelatin;

2. a red-sensitive gelatino-silver iodobromide emulsion coated at a coverage of about 200 mgs./ft. of silver and about I00 mgs./ft. of gelatin;

3. a layer of gelatin coated at a coverage of about 200 mgs./ft.

4. a layer of the magenta dye developer 2-( p-[B-hydroquinonylethyl] -phenylazo)4-isopropoxy-l -naphthol dispersed in gelatin and coated at a coverage of 70 mgsJft. of dye and about mgsJft. of gelatin;

5. a green-sensitive gelatino-silver iodobromide emulsion coated at a coverage of about 100 mg s./ft. of silver and 60 mgsJft. of gelatin;

6. a layer containing 4'-methylphenyl hydroquinone dispersed in gelatin and coated at coverage of about 25 mgs./ft." of 4'-methylphenyl hydroquinone and about 150 mgsJft. of gelatin;

7. a layer of the yellow dye developer 4-(p-[B-hydroquinonylethyl] -phenylazo )-3-( N-n-hexylcarboxamidol phenyl-S-pyrazolone dispersed in gelatin and coated at a coverage of about 40 mgsjtt. of dye and 50 mgsjft. of gelatin;

8. a blue-sensitive gelatino-silver iodobromide emulsion coated at a coverage of about 60 mgsJft. of silver and about 50 mgsJft. of gelatin; and

9. a layer of gelatin coated at a coverage of about 30 mgs./ft. of gelatin.

Then a transparent 4-mil. polyethylene terephthalate film base may be coated, in succession, with the following illustrative layers:

1. the partial butyl ester of polyethylene/maleic anhydride copolymer prepared by refluxing, for l4 hours, 300 grams of high viscosity poly-(ethylene/maleic anhydride), grams of n-butyl alcohol and 1 cc. of 85 percent phosphoric acid to provide a polymeric acid layer approximately 0.75 mil. thick;

2. a 10 percent aqueous emulsion of a diacetone acrylamide/acrylamide copolymer grafted onto a polyvinyl alcohol backbone to provide an inert spacer layer approximately 0.3 mil. thick; and

3. a 2:1 mixture, by weight, of polyvinyl alcohol and poly-4- vinylpyridine, at a coverage of approximately 600 mgs./ft.=, to provide a polymeric image-receiving layer approximately 0.40 mil. thick.

The two components thus prepared may then be taped together in laminate form, at their respective edges, by means of a pressure-sensitive binding tape extending around, in contact with, and over the edges of the resultant laminate.

A rupturable container comprising an outer layer of lead foil and an inner liner or layer of polyvinyl chloride retaining an aqueous alkaline processing solution comprising:

Water I00 cc. Potassium hydroxide I I2 grams Carboxymethyl cellulose 3.4 grams N-benzylu-picolinium bromide l.5 grams Benzotriazole l.0 gram Titanium dioxide 50.0 grams ii may then be fixedly mounted on the leading edge of each of the laminates, by pressure-sensitive tapes interconnecting the respective containers and laminates, such that upon application of compressive pressure to a container its contents would be distributed, upon rupture of the containers marginal seal, between layer 9 and the polymeric image-receiving layer.

A second photosensitive composite film structure identical to the above-described structure may be prepared except that the described polyacrylamide/polyvinyl alcohol graft copolymer layer additionally contains cadmium acetate at a coverage of 690 mgs./ft.*.

The photosensitive laminates may then be exposed through step wedges to selectively filtered radiation incident on the transparent polyethylene terephthalate layer and initially processed, in the absence of actinic radiation, by passage of the exposed film unit through suitable gapped opposed rolls, to efiect rupture of the container and distribution of its contents. The multicolor dye transfer image formation may be viewed through the transparent polyethylene terephthalate film base.

A control and a test film unit containing a metallic salt cross-linking agent prepared substantially as described above were examined spectrophotometrically and the spectral densities are reproduced in FIGS. 8 and 9 with the dashed lines denoting stain which represents undesirable image-forming material present in the image layer.

Both laminates were then placed in an oven, held at 140 F. and 70 percent relative humidity for hours which, experiments have shown, produces the efiect of about 3 months aging. After removal from the oven, the laminates were allowed to cool to room temperature after which they were again examined by a spectrophotometer. The degree of darkening of the control and test laminates are depicted as the solid lines denoted as darkening in FIGS. 8 and 9, respectively. It will be appreciated that not only is the stain level achieved with a system employing the present invention substantially lower than the control, but the degree of darkening over the stain level is far lower in the unit employing the present invention. lt will be accordingly appreciated that by means of the present invention, stabilization of a unified diffusion transfer photographic unit is achieved as to migration of undesired imageforming materials subsequent to substantial image formation.

The pH and solvent concentration of the processing solution initially employed must be a pH at which the dye developers employed are soluble and diffusible. Although it has been found that the specific pH to be employed may be readily determined empirically for any dye developer, or groups of dye developers, most particularly desirable dye developers are soluble at pHs above 9 and relatively insoluble at substantially any alkaline pH, in oxidized form, and the system can be readily balanced accordingly for such dye developers. In addition, although as previously noted, the processing composition, in the preferred embodiment, will include the stated film-forming viscosity-increasing agent, or agents, to facilitate spreading of the composition and to facilitate maintenance of the spread composition as a structurally stable layer of the laminate, during distribution, it is not necessary that such agent be employed as a component of the composition.

Where desired, a polymeric acid layer, for example, of the type discussed above, may be additionally incorporated, as stated, in the film unit of the present invention, to provide reduction of the alkalinity of the processing solution from a pH at which the dyes are soluble to a pH at which the dyes are substantially nondifiusible, in order to advantageously further stabilize the dye transfer image. In such instances, the polymeric acid layer may be positioned intermediate the transparent support and image-receiving layer, and/or the opaque support and next adjacent emulsion/dye unit layer, and the film unit may also contain a polymeric spacer or barrier layer next adjacent the polymeric acid layer, opposite the respective support layer, as previously described.

As disclosed in aforementioned U.S. Pat. No. 3,362,819 the presence of an inert spacer layer was found to be effective in evening out the various reaction rates over a wide range of temperatures, for example, by preventing premature pH reduction when imbibition is effected at temperatures above room temperature, for example, at 95 to l00 F. By providing an inert spacer layer, that application discloses that the rate at which alkali is available for capture in the polymeric acid layer becomes a function of the alkali diffusion rates.

However, as disclosed in U.S. Pat. No. 3,455,686 issued July 15, 1969 in the names of Leonard C. Famey, Howard 0. Rogers and Richard W. Young, preferably the aforemen tioned rate at which the cations of the alkaline processing composition, i.e., alkali ions, are available for capture in the polymeric acid layer should be decreased with increasing transfer processing temperatures in order to provide diffusion transfer color processes relatively independent of positive transfer image variations over an extended range of ambient temperatures.

Specifically, it is there stated to have been found that the diffusion rate of alkali through a permeable inert polymeric spacer layer increases with increased processing temperature to the extent, for example, that at relatively high transfer processing temperatures, that is, transfer processing temperatures above approximately F., a premature decrease in the pH of the transfer processing composition occurs due, at least in part, to the rapid ditfusion of alkali from the dye transfer environment and its subsequent neutralization upon contact with the polymeric acid layer. This was stated to be especially true of alkali traversing an inert spacer layer possessing permeability to alkali optimized to be effective within the temperature range of optimum transfer processing. Conversely, at temperatures below the optimum transfer processing range, for example, temperatures below approximately 40 F., the last-mentioned inert spacer layer was disclosed to provide an effective diffusion barrier timewise preventing effective traverse of the inert spacer layer by alkali having temperature depressed diffusion rates and to result in maintenance of the transfer processing environments high pH for such an extended time interval as to facilitate formation of transfer image stain and its resultant degradation of the positive transfer images color definition.

It is further stated in the last-mentioned U.S. Pat. No. 3,455,686 to have been found, however, that if the inert spacer layer of the print-receiving element is replaced by a spacer layer which comprises a permeable polymeric layer exhibiting permeability inversely dependent on temperature, that is, a polymeric film-forming material which exhibits decreasing permeability to solubilized alkali derived cations such as alkali metal and quaternary ammonium ions under conditions of increasing temperature, that the positive transfer image defects resultant from the aforementioned overextended pH maintenance and/or premature pH reduction are obviated.

As examples of polymers which were disclosed to exhibit inverse temperature-dependent permeability to alkali, mention may be made of: hydroxypropyl polyvinyl alcohol, polyvinyl methyl ether, polyethylene oxide, polyvinyl oxazolidone, hydroxypropyl methyl cellulose, isopropyl cellulose, partial acetals of polyvinyl alcohols such as partial polyvinyl butyral, partial polyvinyl formal, partial polyvinyl acetal, partial polyvinyl propional, and the like. The last-mentioned specified acetals of polyvinyl were stated to generally comprise saturated aliphatic hydrocarbon chains of a molecular weight of at least 1000, preferably of about 1000 to 50,000, possessing a degree of acetalation within about 10 to 30 percent, 10 to 30 percent, 20 to 80 percent, and 10 to 40 percent, of the polyvinyl alcohols theoretical polymeric hydroxy groups, respectively, and including mixed acetals where desired.

Where desired, a mixture of the polymers is to be employed, for example, a mixture of hydroxypropyl methyl cellulose and partial polyvinyl butyral.

Employment of the detailed and preferred film units of the present invention, according to the herein described color diffusion transfer process, specifically provides for the production of a highly stable dye transfer image accomplished, at least in part, by effectively obviating the previously discussed disadvantages of the prior art products and processes, by in situ generation of a substantially continuous, impermeable polymeric layer or stratum having associated therewith a polyvalent metal ion, intermediate the dye image-carrying layer and the photosensitive silver halide emulsion and associated dye image-forming material layers of the film unit, subsequent to substantial dye transfer image formation to provide a barrier to dye image-forming material and processing residues. The stable dye transfer image is obtained irrespective of the fact that the film unit is maintained as an integral laminate unit during exposure, processing, viewing and storage of the unit, and undesired dye image-forming material transfer, of the type previously discussed in detail, subsequent to substantial dye transfer image formation, is effectively prevented by the in situ generated layer composed of filmforming polymers and metal ion. Accordingly, by means of the present invention, multicolor dye transfer images may be provided which exhibit desired maximum and minimum dye transfer image densities; yellow, magenta and cyan dye saturation; red, green and blue hues; and color separation. These unexpected advantages are in addition to the manufacturing advantages obtained by reason of the present inventions integral color transfer film unit and which will be readily apparent from examination of the units parameters, that is, for example, advantages in more efficient utilization of fabricating materials and components, enhanced simplicity of film manufacture and camera design and construction, and more simplified and effectively controlled customer utilization of the unit.

The dimensionally stable support layers referred to may comprise any of the various types of conventional opaque and transparent rigid or flexible materials possessing the requisite liquid impermeability and vapor transmissivity denoted above, and may comprise polymeric films of both synthetic types and those derived from naturally occurring products. Particularly suitable materials include aqueous alkaline solution impermeable, water vapor permeable, flexible polymeric materials such as vapor permeable polymeric films derived from ethylene glycol terephthalic acid, vinyl chloride polymers; polyvinyl acetate; polyamides; polymethacrylic acid methyl and ethyl esters; cellulose derivatives such as cellulose acetate, triacetate, nitrate, propionate, butyrate, acetatepropionate, or acetate-butyrate; alkaline solution impermeable, water vapor permeable papers; cross-linked polyvinyl alcohol; regenerated cellulose; and the like.

It will be noted that the liquid processing composition employed may contain a auxiliary or accelerating developing agent, such as p-methylaminophenol, 2,4-diaminophenol, pbenzylaminophenyl, hydroquinone, toluhydroquinone, phenylhydroquinone, 4'-methylphenylhydroquinone, etc. It is also contemplated to employ a plurality of auxiliary or accelerating developing agents, such as a 3 -pyrazolidone developing agent and a benzenoid developing agent, as disclosed in U.S. Pat. No. 3,039,869, issued June 19, 1962. As examples of suitable combinations of auxiliary developing agents, mention may be made of l-phenyl-3-pyrazolidone in combination with pbenzylaminophenol and l-phenyl-3-pyrazolidone in combination with 2,5-bis-ethylenimino-hydroquinone. Such auxiliary developing agents may be employed in the liquid processing composition or they may be initially incorporated, at least in part, in any one or more of the silver halide emulsion strata, the strata containing the dye developers, the interlayers, the overcoat layer, and the image-receiving layer, or in any other auxiliary layer, or layers, of the film unit. It may be noted that at least a portion of the dye developer oxidized during development may be oxidized and immobilized as a result of a reaction, e.g., an energy-transfer action, with the oxidation product of an oxidized auxiliary developing agent, the latter developing agent being oxidized by the development of exposed silver halide. Such a reaction of oxidized developing agent with unoxidized dye developer would regenerate the auxiliary developing agent for further reaction with the exposed silver halide.

ln addition, development may be effected in the presence of an onium compound, particularly a quaternary ammonium compound, in accordance with the processes disclosed in U.S. Pat. No. 3,173,786, issued Mar. 16, 1965.

it will be apparent that the relative proportions of the agents of the diffusion transfer processing composition may be altered to suit the requirements of the operator. Thus, it is within the scope of this invention to modify the herein described developing compositions by the substitution of preservatives, alkalies, etc., other than those specifically mentioned, provided that the pH of the composition is initially at the first pH and solvent concentration required. When desirable, it is also contemplated to include, in the developing composition, components such as restrainers, accelerators, etc. Similarly, the concentration of various components may be varied over a wide range and when desirable adaptable components may be disposed in the photosensitive element, prior to exposure, in a separate permeable layer of the photosensitive element, and/or in the photosensitive emulsion.

ln all examples of this specification, percentages of components are given by weight unless otherwise indicated.

An extensive compilation of specific dye developers particularly adapted for employment in photographic diffusion transfer processes is set forth in aforementioned U.S. Pat. No. 2,983,606 and in the various copending U.S. applications referred to in that patent, especially in the table of U.S. applications incorporated by reference into the patent as detailed in column 27. As examples of additional U.S. Patents detailing specific dye developers for photographic transfer process use, mention may also be made of U.S. Pat. Nos. 2,983,605; 2,992,106; 3,047,386; 3,076,808; 3,076,820; 3,077,402; 3,126,280; 3,131,061; 3,134,762; 3,134,765; 3,135,604; 3,135,605; 3,135,606; 3,135,734; 3,141,772; 3,142,565; and the like.

As additional examples of synthetic, film-forming permeable polymers particularly adapted to retain dispersed dye developer, mention may be made of nitrocarboxymethyl cellulose, as disclosed in U.S. Pat. No. 2,992,104; an acylamidobenzene sulfo ester of a partial sulfobenzal of polyvinyl alcohol, as disclosed in U.S. Pat. No. 3,043,692; polymers of N-alkyl-a,fi-unsaturated carboxamides and copolymers of N-alky-a,B-carboxamides with N-hydroxyalkyl- B-unsaturated carboxamides, as disclosed in U.S. Pat. No. 3,069,263; copolymers of vinylphthalimide and a,fi-unsaturated carboxylic acids, as disclosed in U.S. Pat. No. 3,061,428; copolymers of N-vinylpyrrolidones and a,fl-unsaturated carboxylic acids and terepolymers of N-vinylpyrrolidones, 01,5- unsaturated carboxylic acids and alkyl esters of a,B-unsaturated carboxylic acids, as disclosed in U.S. Pat. No. 3,044,873; copolymers of N,N-dialkyl-a,B-unsaturated carboxamides with oz,fi-unsaturated carboxylic acids, the corresponding amides of such acids, and copolymers of N-aryland N- cycloalkyl-a,B-unsaturated. carboxamides with a,B-unsaturated carboxylic acids, as disclosed in U.S. Pat. No. 3,069,264; and the like.

in addition to conventional techniques for the direct dispersion of a particulate solid material in a polymeric, or colloidal, matrix such as ball-milling and the like techniques, the preparation of the dye developer dispersion may also be obtained by dissolving the dye in an appropriate solvent, or mixture of solvents, and the resultant solution distributed in the polymeric binder, with optional subsequent removal of the solvent, or solvents, employed, as, for example, by vaporization where the selected solvent, or solvents, possesses a sufficiently low boiling point or washing where the selected solvent, or solvents, possesses a sufficiently high difierential solubility in the wash medium, for example, water, when measured against the solubility of the remaining composition components, and/or obtained by dissolving both the polymeric binder and dye in a common solvent.

For further detailed treatment of solvent distribution systems of the types referred to above, and for an extensive compilation of the conventional solvents traditionally employed in the art to effect distribution of photographic colorproviding materials in polymeric binders, specifically for the formation component layers of photographic film units, reference may be made to U.S. Pat. Nos. 2,269,158; 2,322,027; 2,304,939; 2,304,940; 2,801,171; and the like.

Although the invention has been discussed in detail throughout employing dye developers, the preferred imageproviding materials, it will be readily recognized that other, less preferred, image-providing materials may be substituted in replacement of the preferred dye developers in the practice of the invention. For example, there may be employed dye image-forming materials such as those disclosed in U.S. Pat. Nos. 2,647,049; 2,661,293; 2,698,244; 2,698,798; 2,802,735; 3,148,062; 3,227,550; 3,227,551; 3,227,552; 3,227,554; 3,243,294; 3,330,655; 3,347,671; 3,352,672; 3,364,022; 3,443,939; 3,443,940; 3,443,941; 3,443,943; etc., wherein color diffusion transfer processes are described which employ color coupling techniques comprising, at least in part, reacting one or more color developing agents and one or more color or dye formers or couplers to provide a dye transfer image to a superposed image-receiving layer and those disclosed in U.S. Pat. No. 2,774,668 and 3,087,817, wherein color diffusion transfer processes are described which employ the imagewise differential transfer of complete dyes by the mechanisms therein described to provide a transfer dye image to a contiguous image-receiving layer, and thus including the employment of image-providing material which, as disposed in the film unit, are initially diffusible or nondiffusible in the processing composition selected and are capable of providing an imagewise distribution of processing composition diffusible dye image-forming material as a direct or indirect function of exposure.

For the production of the photosensitive gelatin silver halide emulsions employed to provide the film unit, the silver halide crystals may be prepared by reacting a water-soluble silver salt, such as silver nitrate, with at least one water-soluble halide, such as ammonium, potassium or sodium bromide, preferably together with a corresponding iodide, in an aqueous solution of a peptizing agent such as a colloidal gelatin solution; digesting the dispersion at an elevated temperature, to provide increased crystal growth; washing the resultant dispersion to remove undesirable reaction products and residual water-soluble slats by chilling the dispersion, noodling the set dispersion, and washing the noodles with cold water, or alternatively, employing any of the various flocc systems, or procedures, adapted to effect removal of undesired components, for example, the procedures described in US. Pat. Nos. 2,614,928; 2,614,929; 2,728,662; and the like; afterripening the dispersion at an elevated temperature in combination with the addition of gelatin and various adjuncts, for example, chemical sensitizing agents of U.S. Pat. Nos. 1,574,944; 1,623,499; 2,410,689; 2,597,856; 2,597,915; 2,487,850; 2,518,698; 2,521,926; and the like; all according to the traditional procedures of the art, as described in Neblette, C. 8., Photography Its Materials and Processes, 6th Ed., 1962.

Optical sensitization of the emulsions silver halide crystals may be accomplished by contact of the emulsion composition with an effective concentration of the selected optical sensitizing dyes dissolved in an appropriate dispersing solvent such as methanol ethanol, acetone, water, and the like; all according to the traditional procedures of the art, as described in Hammer, F. M., The Cyanine Dyes and Related Compounds.

Additional optional additives, such as coating aids, hardeners, viscosity-increasing agents, stabilizers, preservatives, and the like, for example, those set forth hereinafter, also may be incorporated in the emulsion formulation, according to the conventional procedures known in the photographic emulsion manufacturing art.

The photoresponsive material of the photographic emulsion will, as previously described, preferably comprise a crystal of silver, for example, one or more of the silver halides such as silver chloride, silver iodide, silver bromide, or mixed silver halides such as silver chlorobromide or silver iodobromide, of varying halide ratios and varying silver concentrations.

The emulsion may include the various adjuncts, or addenda, according to the techniques disclosed in the art.

As zein; binder for the respective emulsion strata, the aforementioned gelatin may be, in whole or in part, replaced with some other colloidal material such as albumin; casein; or zein; or resins such as cellulose derivatives, as described in U.S. Pat. Nos. 2,322,085 and 2,327,808; polyacrylamides, as described in U.S. Pat. No. 2,541,474; vinyl polymers such as described in an extensive multiplicity of readily available U.S. and foreign patents.

Although the preceding description of the invention has been couched in toms of the preferred photosensitive component construction wherein at least two selectively sensitized photosensitive strata are in contiguous coplanar relationship and, specifically, in terms of the preferred tripack-type structure comprising a red-sensitive silver halide emulsion stratum, a green-sensitive silver halide emulsion stratum and a bluesensitive silver halide emulsion stratum having associated therewith, respectively, a cyan dye developer, a magenta dye developer and a yellow dye developer, the photosensitive component of the film unit may comprise at least two sets of selectively sensitized minute photosensitive elements arranged in the form of a photosensitive screen wherein each of the minute photosensitive elements has associated therewith, for example, an appropriate dye developer in or behind its respective silver halide emulsion portion. in general, a suitable photosensitive screen will comprise minute red-sensitized emulsion elements, minute green-sensitized emulsion ele ments and minute blue-sensitized emulsion elements arranged in side-by-side relationship in a screen pattern and having associated therewith, respectively, a cyan, a magenta and a yellow dye developer.

The present invention also includes the employment of a black dye developer and the use of a mixture of dye developers adapted to provide a black and white transfer image, for example, the employment of dye developers of the three subtractive colors in an appropriate mixture in which the quantities of the dye developers are proportioned such that the colors combine to provide black.

Where in the specification, the expression positive image" has been used, this expression should not be interpreted in a restrictive sense since it is used primarily for purposes of illustration, in that it defines the image produced on the imagecarrying layer as being reversed, in the positive-negative sense, with respect to the image of the photosensitive emulsion layers. As an example of an alternative means for positive image," to assume that the photosensitive element is exposed to actinic light through a negative transparency. In this case, the latent image in the photosensitive emulsion layers will be a positive and the dye image produced on the imagecarrying layer will be a negative. The expression positive image is intended to cover such an image produced on the image-carrying layer.

It will be recognized that, by reason of the preferred film units structural parameters, the transfer image formed upon direct exposure of the film unit to a selected subject and processing, will be geometrically reversed image of the subject. Accordingly, to provide transfer image formation geometrically nonreversed, exposure of such film unit should be accomplished through an image reversing optical system such as a camera possessing an image reversing optical system.

1n addition to the described essential layers, it will be recognized that the film unit may also contain one or more subcoats or layers, which, in turn, may contain one or more additives such as plasticizers, intermediate essential layers for the purpose, for example, of improving adhesion, and that any one or more of the described layers may comprise a composite of two or more strata of the same, or different, components and which may be contiguous, or separated from, each other, for example, two or more neutralizing layers or the like, one of which may be disposed intermediate the cyan dye image-founing component retaining layer and the dimensionally stable opaque layer.

Since certain changes may be made in the above product and process without departing from the scope of the invention herein involved, it is intended that all matter contained in the above described or shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.

What is claimed is:

1. A photographic film unit which comprises, in combination:

a photosensitive element comprising a composite structure containing, as essential layers, in sequence, a first dimensionally stable layer opaque to incident actinic radiation; a photosensitive silver halide emulsion layer having associated therewith a dye image-forming material which is processing composition soluble and diffusible as a function of exposure of the photosensitive silver halide emulsion layer to incident actinic radiation; a polymeric layer dyeable by said dye image-forming material; a second dimensionally stable layer transparent to incident actinic radiation; and means securing said layers in substantially fixed relationship;

means for applying a processing composition containing an opacifying agent in a quantity sufficient to mask said dye image-forming material between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto; and

means for interposing a polymeric layer having associated therewith a metal ion capable of cross-linking its polymeric component between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto subsequent to substantial dye image-forming material difiusion to said dyeable polymeric layer upon distribution of said processing composition between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto.

2. A photographic film unit as defined in claim 1 wherein said means for interposing said polymeric layer comprises disposing a polymeric layer permeable to processing composition solubilized dye image-forming material and adapted to be cross-linked by contact with metal ion capable of cross-linking its polymeric component between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent and disposing metal ion adapted to cross-link said dye image-forming material permeable polymeric layer to provide a metal ion cross-linked polymeric layer, in a processing composition permeable layer of said photosensitive element as a metallic salt adapted to solubilized solubilized by contact with distributed processing composition and to diffuse into contact with said dye image-forming material permeable polymeric layer in a concentration effective, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to provide said impermeable metal ion cross-linked polymeric layer.

3. A photographic film unit as defined in claim- 1 wherein said metal ion cross-linked polymeric layer is impermeable to dye image-forming material and means for interposing said dye image-forming material impermeable polymeric layer comprises disposing a polymeric layer penneable to processing composition solubilized dye image-forming material and adapted to be cross-linked by contact with metal ion capable of cross-linking its polymeric component between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent and disposing metal ion adapter to cross-link said dye image-forming material permeable polymeric layer to provide said dye image-forming material impermeable metal ion cross-linked polymeric layer in said processing composition as retained in said rupturable container and adapted to be discharged in functional contact with said dye image-forming material permeable polymeric layer in a concentration effective, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to provide said dye image-forming material impermeable metal ion crosslinked polymeric layer.

4. A photographic film unit as defined in claim 1 wherein said means for interposing said polymeric layer comprises disposing a film-forming polymer adapted to he cross-linked by contact with metal ion capable of cross-linking its polymeric component in said processing composition retained in said rupturable container and adapted upon distribution of said processing composition between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto to provide a substantially continuous dye image-forming material permeable polymeric layer, and said metal ion disposed as a metallic salt in a processing composition permeable layer of said photosensitive element and adapted to be solubilized by contact with distributed processing composition and to diffuse, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to said dye image-forming material permeable polymeric layer in a concentration effective to provide a dye image-forming material impermeable metal ion cross-linked polymeric layer.

5. A photographic film unit as defined in claim 4 wherein said film-forming polymeric material comprises carboxymethyl cellulose.

6. A photographic film unit as defined in claim 5 wherein said metallic salt comprises cadmium acetate.

7. A photographic film unit as defined in claim 6 wherein said metallic salt is disposed in said dyeable polymeric layer.

8. A photographic film unit as defined in claim 4 wherein said film-forming polymeric material comprises carboxymethyl hydroxyethyl cellulose.

9. A photographic film unit as defined in claim 1 wherein said metal ion is polyvalent.

10. A photographic film unit as defined in claim 1 wherein said metal ion is selected from the group consisting of: cadmium, magnesium, calcium, zinc, zirconium, aluminum, chromium, and nickel metal ions.

ll. A photographic film unit as defined in claim 1 wherein said first dimensionally stable layer layer is transparent to incident actinic radiation.

12. A photographic film unit as defined in claim 10 wherein said opacifying agent is initially present intermediate said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto in a quantity sufficient to mask said dye image-providing material.

113. A photographic film unit as defined in claim ll wherein said processing composition is an aqueous alkaline composition.

M. A photographic film unit as defined in claim 13 wherein said dye image-providing material is a dye which is a silver halide developing agent.

IS. A photographic film unit as defined in claim 1 wherein said opacifying agent is present in a quantity sufficient to prevent exposure of said silver halide emulsion during processing in the presence of radiation actinic thereto and incident on said distributed processing solution.

16. A photographic film unit as defined in claim 1 wherein said opacifying agent is actinic radiation reflective.

17. A photographic film unit as defined in claim 16 wherein said opacifying agent is titanium dioxide.

18. A photographic film unit as defined in claim M wherein said photosensitive element comprises at least two selectively sensitized silver halide emulsion layers each having a dye which dye is a silver halide developing agent of a predetermined color associated therewith, each of said dyes soluble and diffusible in processing composition as a function of the point-to-point degree of exposure of the respective emulsion associated therewith.

19. A photographic film unit as defined in claim 18 wherein each of said selectively sensitized photosensitive silver halide emulsions has predominant spectral sensitivity to separate regions of the spectrum and the dye associated with each of said silver halide emulsion layers possesses a spectral absorption range subsequent processing substantially complementary to the predominant sensitivity range of its associated emulsion layer.

20. A photographic film unit as defined in claim 19 wherein each of said silver halide emulsion layers and its associated dye is separated from the next adjacent silver halide emulsion layer and its associated dye by an alkaline solution permeable polymeric interlayer.

21. A photographic film unit as defined in claim 14 including at least one polymeric acid layer positioned intermediate at least one of said first dimensionally stable layers and the photosensitive silver halide emulsion layer next adjacent thereto, and said second dimensionally stable layer and the dyeable polymeric layer adjacent thereto, said processing composition comprises an aqueous alkaline processing composition possessing a first pH at which said dye is soluble and diffusible and said polymeric acid layers possess sufiicient acid capacity to reduce said processing composition from said first pH to a second pH at which said dye is substantially nondiffusible subsequent to substantial dye image diffusion to said dyeable polymeric layer from said silver halide emulsion layer as a function of exposure of said emulsion layer.

22. A photographic film unit as defined in claim 21 which is adapted to be processed by passing said unit between a pair of juxtaposed pressure-applying members and which comprises, in combination:

a photosensitive element including a composite structure containing, as essential layers, in sequence, a dimensionally stable liquid impermeable opaque layer; a redsensitive silver halide emulsion layer having associated therewith cyan dye; a green-sensitive silver halide emulsion layer having associated therewith magenta dye; a blue-sensitive silver halide emulsion layer having associated therewith yellow dye, each of said cyan, magenta and yellow dyes being silver halide developing agents and being soluble and diffusible in aqueous alkaline processing composition at a first pH; an alkaline solution permeable transparent polymeric layer dyeable by said dyes; an alkaline solution permeable transparent polymeric acid .layer containing sufficient acidifying capacity to effect reduction of an aqueous alkaline processing composition having said first pH to a second pH at which said dyes are substantially nondifi'usible; a dimensionally stable liquid impermeable transparent layer; and means securing said layers in substantially fixed relationship;

a rupturable container retaining an aqueous alkaline processing composition fixedly positioned and extending transverse a leading edge of said photosensitive element to effect unidirectional discharge of said containers processing composition between said dyeable polymeric layer and said blue-sensitive silver halide emulsion layer upon application of compressive pressure to said container, said aqueous alkaline processing composition possessing said first pH, opacifying agent in a quantity sufi'rcient to mask said cyan, magenta and yellow dyes associated with said red-, greenand blue-sensitive silver halide emulsion layers and a film-forming polymer adapted to be cross-linked by contact with metal ion capable of cross-linking its polymeric component in a quantity sufficient to provide a substantially continuous, alkaline processing composition solubilized cyan, magenta and yellow dye permeable polymeric layer upon distribution of said aqueous alkaline processing composition intermediate said dyeable polymeric layer and said bluesensitive silver halide emulsion layer; and said metal ion adapted to cross-link said polymeric layer at said second pH disposed as a metallic salt in a processing composition permeable layer of said photosensitive element and adapted to be solubilized by contact with said distributed processing composition and to coact with said cross-linkable polymeric layer in a concentration effective at said second pH to provide an alkaline processing composition solubilized cyan, magenta and yellow dye impermeable metal ion cross-linked polymeric layer intermediate said dyeable polymeric layer and said bluesensitive silver halide emulsion.

23. A photographic film unit as defined in claim 22 wherein said first pH is above 9 and said second pH is below 9.

24. A photographic film unit as defined in claim 22 wherein said metallic salt is cadmium acetate.

25. A photographic film unit as defined in claim 22 wherein said metal ion adapted to cross-link said film-forming polymer at said second pH is disposed in said aqueous alkaline processing composition possessing said first pH as retained in said rupturable container.

26. A photographic film unit in defined in claim 25 wherein said metal ion is nickel ion.

27. A photographic film unit as defined in claim 26 including said metal ion is disposed in a processing composition permeable layer.

28. A photographic film unit as defined in claim 27 wherein said metallic salt is cadmium acetate.

29. A photographic film unit as defined in claim 24 wherein said film-forming polymer is carboxymethyl cellulose.

30, A process for forming transfer images in color which comprises, in combination, the steps of:

a. exposing a photographic film unit which is adapted to be precessed by passing the unit between a pair of juxtaposed pressure-applying members and which includes, in combination, a composite structure comprising a first dimensionally stable layer opaque to incident actinic radiation; a photosensitive silver halide layer having associated therewith a dye image-forming material which is processing composition soluble and diffusible as a function of exposure of the photosensitive silver halide layer to incident actinic radiation; a polymeric layer dyeable by said dye image-forming material; a second dimensionally stable layer transparent to incident actinic radiation; and means securing said layers in substantially fixed relationship; and

a rupturable container retaining a processing composition containing an opacifying agent in a quantity sufficient to mask said dye image-forming material fixedly positioned and extending transverse a leading edge of said photosensitive element to effect unidirectional discharge of said containers alkaline processing composition between said dyeable polymeric layer and the photosensitive silver halide layer next adjacent thereto;

b. applying compressive force to said rupturable container to effect unidirectional discharge of said container's processing composition between said dyeable polymeric layer and the photosensitive silver halide layer next adjacent thereto;

c. effecting thereby development of imagewise halide layer;

image-forming forming thereby an imagewise distribution of mobile dye image-formng material as a function of the point-to-point degree of silver halide layer exposure;

e. transferring, by diffusion, at least a portion of said imagewise distribution of said mobile dye image-providing material to said polymeric layer dyeable by said dye image-forming material to provide a dye image thereto in terms of said distribution;

f. interposing, subsequent to substantial dye transfer image formation and preceding substantial environmental dye transfer image degradation, a polymeric layer inter mediate said dyeable polymeric layer and said silver halide layer next adjacent; said polymeric layer comprising a polymeric material having a metal ion capable of cross linking its polymeric component associated therewith; and

g. maintaining said composite structure intact subsequent to said processing.

31. A process as defined in claim 30 which includes the step of disposing a polymeric layer permeable to processing composition solubilized dye image-forming material and adapted to be cross-linked by contact with said metal ion between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent and disposing metal ion adapted to cross-link said dye image-forming material permeable polymeric layer to provide a dye image-forming material impermeable metal ion cross-linked polymeric layer in a processing composition permeable layer of said photosensitive element as a metallic salt adapted to be solubilized by contact with distributed processing composition and to diffuse into contact with said dye image-forming material permeable polymeric layer in a concentration effective, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to provide said dye image-forming material impermeable metal ion cross-linked polymeric layer.

32. A process as defined in claim 30 which includes the step of disposing a polymeric material penneable to processing composition solubilized dye image-forming material and adapted to be cross-linked by contact with said metal ion between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent and disposing said metal ion adapted to cross-link said dye image-forming material permeable polymeric layer to provide a dye imagefonning material impermeable metal ion cross-linked polymeric layer in said processing composition as retained in said rupturable container and adapted to be discharged in functional contact with said dye image-forming material permeable polymeric material in a concentration efiective, subsequent to substantial dye image-fuming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to provide said dye image-forming material impermeable metal ion cross-linked polymeric layer.

33. A process as defined in claim 30 which includes the step of disposing a film-forming polymer adapted to be crosslinked by contact with said metal ion in said processing composition retained in said rupturable container and adapted upon distribution of said processing composition between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto to provide a substantially continuous dye image-forming material permeable polymeric layer, and said metal ion disposed as a metallic salt in a processing composition permeable layer of said photosensitive element and adapted to be solubilized by contact with distributed processing composition and to diffuse, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to said dye image-forming material permeable polymeric layer in a concentration effective to proved a dye image-forming material impermeable metal ion cross-linked polymeric layer.

34. A process as defined in claim 33 wherein said film-forming polymeric material comprises carboxymethyl cellulose.

35. A process as defined in claim 34 wherein said metallic salt comprises cadmium acetate.

36. A process as defined in claim 35 wherein said metallic salt is disposed in said dyeable polymeric layer.

37. A process as defined in claim 33 wherein said film-fanning polymeric material comprises carboxymethyl hydroxyethyl cellulose.

38. A process as defined in claim 30 wherein said metal ion is polyvalent.

39. A process as defined in claim 38 wherein said metal ion is selected from the group consisting of: cadmium, magnesium, calcium, zinc, zirconium, aluminum, chromium, and

dimensionally stable layer is transparent to incident actinic radiation.

41. A process as defined in claim 40 wherein said opacifying agent is initially present intermediate said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto in a quantity sufficient to mask said dye image-fonning material.

42. A process as defined in claim 30 wherein said dye image-forming material is a dye which is a silver halide developing agent.

43. A process as defined in claim 42 wherein said photographic film unit includes at least two selectively sensitized silver halide emulsion layers, each of said silver halide emulsions having associated therewith a dye, which is a silver halide developing agent, of predetermined color.

44. A process as defined in claim 43 wherein each of said selectively sensitized silver halide emulsion layers possesses predominant spectral sensitivity to a separate region of the spectrum and the dye associated with each of said emulsion layers possesses a spectral absorption range subsequent to processing substantially complementary to the predominant sensitivity range of its associated emulsion.

45. A process as defined in claim 42 wherein said composition is an aqueous alkaline composition.

46. A process as defined in claim 45 wherein said composite structure includes at least one polymeric acid layer positioned intermediate at least one of said first dimensionally stable layers and the next adjacent photosensitive silver halide layer, and said second dimensionally stable layer and the next adjacent dyeable polymeric layer and said polymeric acid layers containing sufficient acidifying groups to effect reduction of an aqueous alkaline processing composition possessing a first pH at which said dyes are substantially soluble and difiusible to a second pH at which said dyes are substantially nondiffusible and including the step of transferring, by diffusion, subsequent to substantial transfer image formation, a sufi'rcient portion of the ions of said alkaline processing solution to said polymeric acid layers to thereby reduce the alkalinity of said solution from said first pH to said second pH.

47. A process as defined in claim 46 wherein said metal ion is adapted to cross-link said polymeric layer intennediate said dyeable polymeric layer and said silver halide layer at said second pH.

48. A process as defined in claim 47 wherein said metal ion is disposed in said aqueous alkaline processing composition possessing said first pH as contained in said rupturable container.

49. A process as defined in claim 48 wherein said aqueous alkaline processing composition additionally contains a filmforming polymeric material adapted to be cross-linked by contact with said metal ion at said second pH in a quantity sufficient to provide said polymeric layer intennediate said said dyeable polymeric layer and said silver halide layer upon said distribution of said processing composition.

50. A process as defined in claim 49 wherein said metal ion is zirconia and said film-forming polymeric material is carboxymethyl cellulose and hydroxyethyl cellulose.

51. A process as defined in claim 30 wherein a metallic salt providing first metal ion is disposed in said polymeric layer dyeable by said dye image-forming material and second metal ion is disposed in said processing composition.

52. A process as defined in claim 51 wherein said metallic salt is cadmium acetate and said second metal ion is nickel.

53. A process as defined in claim 30 wherein said opacifying agent is titanium dioxide.

54. A process as defined in claim 30 including the step of separating said container from said composite structure subsequent to substantial transfer image formation.

UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3 ,6l9,l55 Dated November 9, 1971 Inventoz-(s) Richard W. Young It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

In the Abstract:

Delete line 13; and line 24 delete "and".

In the Claims:

Column 21, line 54, after "to" insert --be; and delete "solubilized" second occurrence;

line 61, delete "said" and insert -a dye imageforming material,-

line 63, delete "metal ion cross-linked polymeric layer is impermeable to" line 72, delete "adapter" and substitute adapted-; and

line 75, delete "said" and substitute a.

Column 22, line 13, delete "said" second occurrence and substitute a-; and

line 50, delete "l0" and substitute l-.

Column 23, line 8, after "subsequent" insert --to.

Column 24, line 21, delete "in" and substitute as;

line 34, delete "precessed" and substitute processed;

line 64, delete "dye image-forming material and"

Claims

2. A photographic film unit as defined in claim 1 wherein said means for interposing said polymeric layer comprises disposing a polymeric layer permeable to processing composition solubilized dye image-forming material and adapted to be cross-linked by contact with metal ion capable of cross-linking its polymeric component between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent and disposing metal ion adapted to cross-link said dye image-forming material permeable polymeric layer to provide a metal ion cross-linked polymeric layer, in a processing composition permeable layer of said photosensitive element as a metallic salt adapted to solubilized solubilized by contact with distributed processing composition and to diffuse into contact with said dye image-forming material permeable polymeric layer in a concentration effective, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to provide said impermeable metal ion cross-linked polymeric layer.
3. A photographic film unit as defined in claim 1 wherein said metal ion cross-linked polymeric layer is impermeable to dye image-forming material and means for interposing said dye image-forming material impermeable polymeric layer comprises disposing a polymeric layer permeable to processing composition solubilized dye image-forming material and adapted to be cross-linked by contact with metal ion capable of cross-linking its polymeric component between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent and disposing metal ion adapter to Cross-link said dye image-forming material permeable polymeric layer to provide said dye image-forming material impermeable metal ion cross-linked polymeric layer in said processing composition as retained in said rupturable container and adapted to be discharged in functional contact with said dye image-forming material permeable polymeric layer in a concentration effective, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to provide said dye image-forming material impermeable metal ion cross-linked polymeric layer.
4. A photographic film unit as defined in claim 1 wherein said means for interposing said polymeric layer comprises disposing a film-forming polymer adapted to be cross-linked by contact with metal ion capable of cross-linking its polymeric component in said processing composition retained in said rupturable container and adapted upon distribution of said processing composition between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto to provide a substantially continuous dye image-forming material permeable polymeric layer, and said metal ion disposed as a metallic salt in a processing composition permeable layer of said photosensitive element and adapted to be solubilized by contact with distributed processing composition and to diffuse, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to said dye image-forming material permeable polymeric layer in a concentration effective to provide a dye image-forming material impermeable metal ion cross-linked polymeric layer.
5. A photographic film unit as defined in claim 4 wherein said film-forming polymeric material comprises carboxymethyl cellulose.
6. A photographic film unit as defined in claim 5 wherein said metallic salt comprises cadmium acetate.
7. A photographic film unit as defined in claim 6 wherein said metallic salt is disposed in said dyeable polymeric layer.
8. A photographic film unit as defined in claim 4 wherein said film-forming polymeric material comprises carboxymethyl hydroxyethyl cellulose.
9. A photographic film unit as defined in claim 1 wherein said metal ion is polyvalent.
10. A photographic film unit as defined in claim 1 wherein said metal ion is selected from the group consisting of: cadmium, magnesium, calcium, zinc, zirconium, aluminum, chromium, and nickel metal ions.
11. A photographic film unit as defined in claim 1 wherein said first dimensionally stable layer layer is transparent to incident actinic radiation.
12. A photographic film unit as defined in claim 10 wherein said opacifying agent is initially present intermediate said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto in a quantity sufficient to mask said dye image-providing material.
13. A photographic film unit as defined in claim 1 wherein said processing composition is an aqueous alkaline composition.
14. A photographic film unit as defined in claim 13 wherein said dye image-providing material is a dye which is a silver halide developing agent.
15. A photographic film unit as defined in claim 1 wherein said opacifying agent is present in a quantity sufficient to prevent exposure of said silver halide emulsion during processing in the presence of radiation actinic thereto and incident on said distributed processing solution.
16. A photographic film unit as defined in claim 1 wherein said opacifying agent is actinic radiation reflective.
17. A photographic film unit as defined in claim 16 wherein said opacifying agent is titanium dioxide.
18. A photographic film unit as defined in claim 14 wherein said photosensitive element comprises at least two selectively sensitized silver halide emulsion layers eAch having a dye which dye is a silver halide developing agent of a predetermined color associated therewith, each of said dyes soluble and diffusible in processing composition as a function of the point-to-point degree of exposure of the respective emulsion associated therewith.
19. A photographic film unit as defined in claim 18 wherein each of said selectively sensitized photosensitive silver halide emulsions has predominant spectral sensitivity to separate regions of the spectrum and the dye associated with each of said silver halide emulsion layers possesses a spectral absorption range subsequent processing substantially complementary to the predominant sensitivity range of its associated emulsion layer.
20. A photographic film unit as defined in claim 19 wherein each of said silver halide emulsion layers and its associated dye is separated from the next adjacent silver halide emulsion layer and its associated dye by an alkaline solution permeable polymeric interlayer.
21. A photographic film unit as defined in claim 14 including at least one polymeric acid layer positioned intermediate at least one of said first dimensionally stable layers and the photosensitive silver halide emulsion layer next adjacent thereto, and said second dimensionally stable layer and the dyeable polymeric layer adjacent thereto, said processing composition comprises an aqueous alkaline processing composition possessing a first pH at which said dye is soluble and diffusible and said polymeric acid layers possess sufficient acid capacity to reduce said processing composition from said first pH to a second pH at which said dye is substantially nondiffusible subsequent to substantial dye image diffusion to said dyeable polymeric layer from said silver halide emulsion layer as a function of exposure of said emulsion layer.
22. A photographic film unit as defined in claim 21 which is adapted to be processed by passing said unit between a pair of juxtaposed pressure-applying members and which comprises, in combination: a photosensitive element including a composite structure containing, as essential layers, in sequence, a dimensionally stable liquid impermeable opaque layer; a red-sensitive silver halide emulsion layer having associated therewith cyan dye; a green-sensitive silver halide emulsion layer having associated therewith magenta dye; a blue-sensitive silver halide emulsion layer having associated therewith yellow dye, each of said cyan, magenta and yellow dyes being silver halide developing agents and being soluble and diffusible in aqueous alkaline processing composition at a first pH; an alkaline solution permeable transparent polymeric layer dyeable by said dyes; an alkaline solution permeable transparent polymeric acid layer containing sufficient acidifying capacity to effect reduction of an aqueous alkaline processing composition having said first pH to a second pH at which said dyes are substantially nondiffusible; a dimensionally stable liquid impermeable transparent layer; and means securing said layers in substantially fixed relationship; a rupturable container retaining an aqueous alkaline processing composition fixedly positioned and extending transverse a leading edge of said photosensitive element to effect unidirectional discharge of said container''s processing composition between said dyeable polymeric layer and said blue-sensitive silver halide emulsion layer upon application of compressive pressure to said container, said aqueous alkaline processing composition possessing said first pH, opacifying agent in a quantity sufficient to mask said cyan, magenta and yellow dyes associated with said red-, green- and blue-sensitive silver halide emulsion layers and a film-forming polymer adapted to be cross-linked by contact with metal ion capable of cross-linking its polymeric component in a quantity sufficient to provide a substantially continuous, alkaline processing composition solubilized cyan, magenta and yellow dye permeable polymeric layer upon dIstribution of said aqueous alkaline processing composition intermediate said dyeable polymeric layer and said blue-sensitive silver halide emulsion layer; and said metal ion adapted to cross-link said polymeric layer at said second pH disposed as a metallic salt in a processing composition permeable layer of said photosensitive element and adapted to be solubilized by contact with said distributed processing composition and to coact with said cross-linkable polymeric layer in a concentration effective at said second pH to provide an alkaline processing composition solubilized cyan, magenta and yellow dye impermeable metal ion cross-linked polymeric layer intermediate said dyeable polymeric layer and said blue-sensitive silver halide emulsion.
23. A photographic film unit as defined in claim 22 wherein said first pH is above 9 and said second pH is below 9.
24. A photographic film unit as defined in claim 22 wherein said metallic salt is cadmium acetate.
25. A photographic film unit as defined in claim 22 wherein said metal ion adapted to cross-link said film-forming polymer at said second pH is disposed in said aqueous alkaline processing composition possessing said first pH as retained in said rupturable container.
26. A photographic film unit in defined in claim 25 wherein said metal ion is nickel ion.
27. A photographic film unit as defined in claim 26 including said metal ion is disposed in a processing composition permeable layer.
28. A photographic film unit as defined in claim 27 wherein said metallic salt is cadmium acetate.
29. A photographic film unit as defined in claim 24 wherein said film-forming polymer is carboxymethyl cellulose.
30. A process for forming transfer images in color which comprises, in combination, the steps of: a. exposing a photographic film unit which is adapted to be precessed by passing the unit between a pair of juxtaposed pressure-applying members and which includes, in combination, a composite structure comprising a first dimensionally stable layer opaque to incident actinic radiation; a photosensitive silver halide layer having associated therewith a dye image-forming material which is processing composition soluble and diffusible as a function of exposure of the photosensitive silver halide layer to incident actinic radiation; a polymeric layer dyeable by said dye image-forming material; a second dimensionally stable layer transparent to incident actinic radiation; and means securing said layers in substantially fixed relationship; and a rupturable container retaining a processing composition containing an opacifying agent in a quantity sufficient to mask said dye image-forming material fixedly positioned and extending transverse a leading edge of said photosensitive element to effect unidirectional discharge of said container''s alkaline processing composition between said dyeable polymeric layer and the photosensitive silver halide layer next adjacent thereto; b. applying compressive force to said rupturable container to effect unidirectional discharge of said container''s processing composition between said dyeable polymeric layer and the photosensitive silver halide layer next adjacent thereto; c. effecting thereby development of imagewise halide layer; image-forming forming thereby an imagewise distribution of mobile dye image-formng material as a function of the point-to-point degree of silver halide layer exposure; e. transferring, by diffusion, at least a portion of said imagewise distribution of said mobile dye image-providing material to said polymeric layer dyeable by said dye image-forming material to provide a dye image thereto in terms of said distribution; f. interposing, subsequent to substantial dye transfer image formation and preceding substantial environmental dye transfer image degradation, a polymeric layer intermediate said dyeable polymeric layer and said silver halide layer next adjacent; said polymeric layer comprising a polymeric material having a metal ion capable of cross-linking its polymeric component associated therewith; and g. maintaining said composite structure intact subsequent to said processing.
31. A process as defined in claim 30 which includes the step of disposing a polymeric layer permeable to processing composition solubilized dye image-forming material and adapted to be cross-linked by contact with said metal ion between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent and disposing metal ion adapted to cross-link said dye image-forming material permeable polymeric layer to provide a dye image-forming material impermeable metal ion cross-linked polymeric layer in a processing composition permeable layer of said photosensitive element as a metallic salt adapted to be solubilized by contact with distributed processing composition and to diffuse into contact with said dye image-forming material permeable polymeric layer in a concentration effective, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to provide said dye image-forming material impermeable metal ion cross-linked polymeric layer.
32. A process as defined in claim 30 which includes the step of disposing a polymeric material permeable to processing composition solubilized dye image-forming material and adapted to be cross-linked by contact with said metal ion between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent and disposing said metal ion adapted to cross-link said dye image-forming material permeable polymeric layer to provide a dye image-forming material impermeable metal ion cross-linked polymeric layer in said processing composition as retained in said rupturable container and adapted to be discharged in functional contact with said dye image-forming material permeable polymeric material in a concentration effective, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to provide said dye image-forming material impermeable metal ion cross-linked polymeric layer.
33. A process as defined in claim 30 which includes the step of disposing a film-forming polymer adapted to be cross-linked by contact with said metal ion in said processing composition retained in said rupturable container and adapted upon distribution of said processing composition between said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto to provide a substantially continuous dye image-forming material permeable polymeric layer, and said metal ion disposed as a metallic salt in a processing composition permeable layer of said photosensitive element and adapted to be solubilized by contact with distributed processing composition and to diffuse, subsequent to substantial dye image-forming material transfer to said dyeable polymeric layer from said associated silver halide emulsion layer as a function of exposure of said emulsion layer, to said dye image-forming material permeable polymeric layer in a concentration effective to proved a dye image-forming material impermeable metal ion cross-linked polymeric layer.
34. A process as defined in claim 33 wherein said film-forming polymeric material comprises carboxymethyl cellulose.
35. A process as defined in claim 34 wherein said metallic salt comprises cadmium acetate.
36. A process as defined in claim 35 wherein said metallic salt is disposed in said dyeable polymeric layer.
37. A process as defined in claim 33 wherein said film-forming polymeric material comprises carboxymethyl hydroxyethyl cellulose.
38. A process as defined in claim 30 wherein said metal ion is polyvalent.
39. A process as defined in claim 38 wherein said metal ion is selecteD from the group consisting of: cadmium, magnesium, calcium, zinc, zirconium, aluminum, chromium, and nickel metal ions.
40. A process as defined in claim 30 wherein said first dimensionally stable layer is transparent to incident actinic radiation.
41. A process as defined in claim 40 wherein said opacifying agent is initially present intermediate said dyeable polymeric layer and the photosensitive silver halide emulsion layer next adjacent thereto in a quantity sufficient to mask said dye image-forming material.
42. A process as defined in claim 30 wherein said dye image-forming material is a dye which is a silver halide developing agent.
43. A process as defined in claim 42 wherein said photographic film unit includes at least two selectively sensitized silver halide emulsion layers, each of said silver halide emulsions having associated therewith a dye, which is a silver halide developing agent, of predetermined color.
44. A process as defined in claim 43 wherein each of said selectively sensitized silver halide emulsion layers possesses predominant spectral sensitivity to a separate region of the spectrum and the dye associated with each of said emulsion layers possesses a spectral absorption range subsequent to processing substantially complementary to the predominant sensitivity range of its associated emulsion.
45. A process as defined in claim 42 wherein said composition is an aqueous alkaline composition.
46. A process as defined in claim 45 wherein said composite structure includes at least one polymeric acid layer positioned intermediate at least one of said first dimensionally stable layers and the next adjacent photosensitive silver halide layer, and said second dimensionally stable layer and the next adjacent dyeable polymeric layer and said polymeric acid layers containing sufficient acidifying groups to effect reduction of an aqueous alkaline processing composition possessing a first pH at which said dyes are substantially soluble and diffusible to a second pH at which said dyes are substantially nondiffusible and including the step of transferring, by diffusion, subsequent to substantial transfer image formation, a sufficient portion of the ions of said alkaline processing solution to said polymeric acid layers to thereby reduce the alkalinity of said solution from said first pH to said second pH.
47. A process as defined in claim 46 wherein said metal ion is adapted to cross-link said polymeric layer intermediate said dyeable polymeric layer and said silver halide layer at said second pH.
48. A process as defined in claim 47 wherein said metal ion is disposed in said aqueous alkaline processing composition possessing said first pH as contained in said rupturable container.
49. A process as defined in claim 48 wherein said aqueous alkaline processing composition additionally contains a film-forming polymeric material adapted to be cross-linked by contact with said metal ion at said second pH in a quantity sufficient to provide said polymeric layer intermediate said said dyeable polymeric layer and said silver halide layer upon said distribution of said processing composition.
50. A process as defined in claim 49 wherein said metal ion is zirconia and said film-forming polymeric material is carboxymethyl cellulose and hydroxyethyl cellulose.
51. A process as defined in claim 30 wherein a metallic salt providing first metal ion is disposed in said polymeric layer dyeable by said dye image-forming material and second metal ion is disposed in said processing composition.
52. A process as defined in claim 51 wherein said metallic salt is cadmium acetate and said second metal ion is nickel.
53. A process as defined in claim 30 wherein said opacifying agent is titanium dioxide.
54. A process as defined in claim 30 including the step of separating said container from said composite structure subsequent to substantial transfer image formation.