US3743504A - Developer scavengers for image transfer systems - Google Patents

Abstract

A DEVELOPER SCAVENGER LAYER COMPRISING AN ALDEHYDEBISULFITE ADDITION PRODUCT AND A POLYMERIC BINDER IS USEFUL FOR REDUCING BACKGROUND STAIN IN A DYE IMAGE-RECEIVING ELEMENT OF A COLOR DIFFUSION TRANSFER SYSTEM UTILIZING IMMOBILE COUPLERS WHICH FORM DIFFUSIBLE DYES.

Description

United States Patent 3,743,504 DEVELOPER SCAVENGERS FOR IMAGE TRANSFER SYSTEMS Glen M. Dappen, Webster, Donald A. Smith, Irondequoit,

N.Y., assignors to Eastman Kodak Company, Rochester, N.Y.

No Drawing. Filed May 28, 1971, Ser. No. 148,138 Int. Cl. G03c 7/00, /54, N60 US. Cl. 96-3 27 Claims ABSTRACT OF THE DISCLOSURE A developer scavenger layer comprising an aldehydebisulfite addition product and a polymeric binder is useful for reducing background stain in a dye image-receiving element of a color diffusion transfer system utilizing immobile couplers which form diffusible dyes.

This invention relates to the art of photography, and more particularly to color diffusion transfer film systems, dye image-receiving elements and methods for obtaining positive, right-reading diffusion transfer dye images with reduced color developer stain.

US. Pat. 3,445,338 of Beavers et al., issued May 20, 1969, describes a receiving sheet for use in a dye diffusion transfer process utilizing aromatic primary arnino color developing agents. The receiving sheet comprises a support having thereon a nondiffusible acid material, an interlayer containing finely divided white pigment and a mordant layer. The acid layer terminates development by lowering the pH of the alkaline developer composition and apparently also functions to salt out residual color developer. The pigmented layer functions to mask the stain formed in the underlying layer.

It is an object of this invention to provide a novel dye image-receiving element wherein a developer scavenger layer is employed which effectively destroys any residual color developer by forming a colorless reaction product, thereby eliminating the need for a pigmented masking layer.

Another object of this invention is to provide timing means in connection with the developer scavenger layer so that development in the photosensitive element is substantially complete before the developer scavenger layer becomes operative.

It is another object of this invention to reduce the formation of the yellowish-brown stain which appears in color diffusion transfer image-receiving layers and is caused by the aerial oxidation of unused color developer present in the layer.

Still another object of this invention is to provide color transfer film units and methods for processing same wherein the dye image-receiving layer is integral with the photosensitive element itself or is provided on a separate support to be superposed on the photosensitive element after exposure thereof.

These and other objects are achieved by a photographic film unit according to our invention, which is adapted to be processed by passing the unit between a pair of juxtaposed pressure-applying members, such as would be found in a camera designed for in-camera processing, comprising:

(a) A photosensitive element comprising a support having thereon at least one and preferably three, photosensitive silver halide emulsion layers, each silver halide emulsion layer having associated therewith a dye imageproviding material comprising a nondiffusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a diifusible dye;

(b) A dye image-receiving layer; and

(c) A rupturable container containing an alkaline ice processing composition and which is adapted to be positioned during processing of the film unit so that a compressive force applied to the container by the pressureapplying members will effect a discharge of the containers contents within the film unit;

the above film unit containing an aromatic primary amino color developing agent, preferably in the rupturable container and an aldehyde-bisulfite addition product in a polymeric binder which is capable of reacting with unused aromatic primary amino color developing agent to form a colorless reaction product.

The developer-scavenging, aldehyde-bisulfite addition products or adducts employed in our invention have the following general formula:

polymers or copolymers having recurring units of the following formula: (III) OH C- HO-(BH-SOQM wherein R represents a hydrogen atom or an alkyl group, including a substituted alkyl group, preferably a lower alkyl group, i.e., having 1 to 6 carbon atoms in the chain such as methyl, ethyl, isopropyl, benzyl, hexyl, carbethoxymethyl, etc.; n represents an integer of from 1 to 6; and M represents an alkali metal ion, e.g., a sodium, potassium or ammonium ion. The molecular weight of the polymers and copolymers is at least about 500 and preferably greater than 2000.

Examples of monomeric, developer-scavenging, aldehyde-bisulfite addition products or salt adducts coming within the scope of Formulas I and II include:

OH H-(lH-SOaNa sodium formaldehyde bisulfite adduct (|)H CH3-CHSOaNa sodium acetaldehyde bisulfite adduct (I)H CHg-CH -CH -OH-SOSK potassium butyraldehyde bisulfite ndduct (|)H CHs-CH GH CHSOaNa sodium butyraldehyde bisulfite ndduct OH CH3-CH HSOaNa sodium prop'ionaldehyde bisulfite adduct OH OHS-OHz-H-SOSK potassium propionaldehyde blsulfite a-dduet CH1; OH CH3H-( JH-SOaNa sodium isobutyraldehyde bisulfite adduct C| H 0H NaO3SOHCH CHg-(lHSO3Na bis(sodium succinaldehyde bisulfite) adduct OH OH KOaS-H-CHg-OHz-H-SO3K bis(potassium succinaldehyde bisulfite) adduct OH OH bis(sodium glutaraldehyde bisulfite) adduct OH OH Especially good results are obtained with the use of sodium formaldehyde bisulfite adduct, sodium acetaldehyde bisulfite adduct, bis(sodium succinaldehyde bisulfite) adduct, bis(sodium glutaraldehyde bisulfite) adduct or combinations thereof.

Examples of polymers and copolymers within the scope of Formula III above include homopolymers of acrylaldehyde sodium bisulfite adducts or methacrylaldehyde sodium bisulfite adducts and copolymers of these adducts with vinyl compounds such as unsaturated acids, e.g., acrylic acid and methacrylic acid; acrylic esters, e.g., methyl acrylate and propyl acrylate; methacrylic esters, e.g. methyl methacrylate and ethyl methylacrylate; acrylamides, e.g., acrylamide and isopropyl acrylamide; and methacrylamides, e.g., methacrylamide, and N-methyl-methacrylamide.

The described developer-scavenging, aldehyde-bisulfite adducts can be employed at any concentration useful for the intended purpose. Generally, an effective concentration is from about 250 mg. per square foot of support to about 1500 mg. per square foot of support. Especially good results are obtained at a concentration of from about 500 mg. per square foot of support to about 1250 mg. per square foot of support.

The aldehyde-bisulfite addition product of our invention may be dispersed in any polymeric binder suitable for the intended purpose, e.g., gelatin, proteins, cellulose derivatives, polysaccharides, polyvinyl compounds, acrylamide polymers and copolymers, etc. In addition, in embodiments of our invention where the developer scavenger material itself is a polymer, no additional polymeric binder may be needed, i.e., the polymeric scavenger material can serve as the polymeric binder.

It is believed that the aldehyde-bisulfite adduct functions as a developer scavenger precursor and under the basic conditions of color development reverts to the parent aldehyde compound which in turn reacts with excess unused aromatic primary amino color developing agent to form a colorless product, thereby reducing the yellowish-brown stain which results from the diffusion of unused aromatic primary amino color developing agent into the image-receiving element. Therefore, any aldehydebisulfite addition product which is compatible with the photosensitive and image-receiving elements can be employed in the practice of the invention provided the addition product reverts under alkaline conditions to the parent aldehyde compound which in turn will react with primary amino color developing agent to form a colorless product. In addition, the alkali metal bisulfite which is liberated reacts with alkali present thereby lowering the pH of the system, e.g.,

The developer scavenger layer of our invention can be used not only in diffusion transfer systems wherein the image-receiving element is located on a separate support from the photosensitive element but also in diffusion transfer systems wherein the image-receiving element is integral with the photosensitive element.

In one embodiment of our invention wherein the imagereceiving element is separate from the photosensitive element, the novel dye image-receiving element comprises a support having thereon the following layers:

(a) a developer-scavenger layer comprising an aldehydebisulfite adduct in a polymeric binder, and (b) a dye image-receiving layer.

A timing layer, described hereinafter, can also be employed in the invention between the developer-scavenging layer and the dye image-receiving layer which functions to delay the rate of diffusion of aromatic primary ammo color developing agent into the developer-scavengmg layer. The timing layer, therefore, ensures the efficient use of the aromatic primary amino color developing agent in the photosensitive element prior to developer-scavenging action by the aldehyde-bisulfite adduct. A pH-lowering material, described hereinafter, can also be employed in the dye image-receiving element to increase the stability of the transferred image. Although not required, a lightreflective layer comprising a white pigment in a binder, described hereinafter, can also be employed in the dye image-receiving element, if desired. The light-reflective layer can be located underneath the dye image-receiving layer or can be combined with the timing layer if one is employed.

The above-described dye image-receiving element of the film unit is adapted to be superposed on the photosensitive element after exposure thereof. The development and transfer operations can be effected by bathing either or both the exposed photosensitive element and the dye image-receiving element in a deveolping solution before rolling into contact with each other or a viscous develop ing composition can be placed between the elements for spreading in a predetermined amount across and into contact with the exposed surface of the photosensitive element. The viscous developing composition is desirably utilized in one or more pods attached to the reception sheet or photosensitive element that can be readily ruptured when development is desired as described, for example, in US. Pats. 2,559,643; 2,647,049; 2,661,293; 2,698,- 244; 2,698,798 and 2,774,668.

During the development phase of a color diffusion transfer process according to our invention, the image dyes formed in the respective blue, green and red-sensitive silver halide emulsion layers diffuse out of the photosensitive element through the viscous developer composition and into the dye image-receiving layer, e.g. into the dye image-receiving element described above, where the dyes are mordanted to form the transferred image. The timing layer, if one is present, prevents the dilfusion of color developer into the scavenger layer for the time necessary to ensure the efficient use of the aromatic primary amino color developing agent in the photosensitive element. Upon separation, it is believed that the unused aromatic primary amino color developing agent diffuses into the developer-scavenger layer where the developer molecules react with the aldehyde compounds which have been liberated from the aldehyde-bisulfite adducts under alkaline conditions of development to form a colorless product. Regardless of the mechanism involved, a marked decrease in the yellowish-brown stain caused by the presence of unused color developing agent in color development diffusion transfer image-receiving elements is observed upon utilizing a developer-scavenger layer comprising an aldehyde-bisulfite adduct dispersed in a suitable binder, preferably in the image-receiving element.

In another embodiment of our invention, the developer-scavenger layer can be located in an integral film unit wherein the dye image-receiving layer is located integral with the photosensitive element between the support and the lowermost photosensitive silver halide emulsion layer. A general format for integral receiver-negative photosensitive elements is described in copending US. application Ser. No. 027,991 of Barr, Bush and Thomas, filed Apr. 13, 1970 and now abandoned. In such an embodiment, the support for the photosensitive element is transparent and is coated with the dye image-receiving layer, a substantially opaque, light-reflective layer, e.g. TiO a developer scavenger layer comprising an aldehyde-bisulfite adduct dispersed in a suitable binder, and the various layers forming the color-forming units. After exposure of the photosensitive element, a rupturable container containing an alkaline processing composition and an opaque process sheet are brought into superposed position. Pressure-applying members in a camera rupture the container and spread processing composition over the photosensitive element as the film unit is Withdrawn from the camera. The processing composition develops the exposed silver halide layers and dye images are formed as a function of development which diffuse to the imagereceiving layer to provide a positive, right-reading image which is viewed through the transparent support on the opaque reflecting layer background. It is believed that positioning of the developer-scavenger layer between the color-forming photosensitive units and the imagereceiving layer in the integral receiver-negative lfilm system prevents the diffusion of unused color developer into the image-receiving layer. If desired, the developer scavenger layer comprising the aldehyde-bisulfite adducts described herein can be located in the opaque process sheet. For further details concerning the format of this particular integral film unit, its preparation and use, reference is made to the above-mentioned U.S. application Ser. No. 027,991 of Barr, Bush and Thomas, filed Apr. 13, 1970.

Another format for integral receiver-negative photosensitive systems in which our invention can be employed is described in U.S. Ser. No. 027,990 of Cole, filed Apr. 13, 1970 and noW abandoned. In such an embodiment, the support for the color diffusion transfer system is transparent and is coated with the image-receiving layer, a substantially opaque, light-reflective layer, e.g. TiO a developer scavenger layer comprising an aldehyde-bisulfite adduct dispersed in a suitable binder, and then the various layers forming the color-forming units and a top transparent sheet. A rupturable container containing an alkaline processing composition and an opacifier is positioned adjacent to the top layer and sheet. The film unit is placed in a camera, exposed through the top transparent sheet and then passed between a pair of pressureapplying members in the camera as it is being removed therefrom. The pressure-applying members rupture the container and spread processing composition and opacifier over the negative portion of the film unit to render it lightinsensitive. The processing composition develops the exposed silver halide layers and dye images are formed as a result of development which diffuse to the image-receiving layer to provide positive, right-reading image which is viewed through the transparent support on the opaque reflecting layer background. Any unused aromatic primary amino color developing agent which may diffuse in the direction of the image-receiving layer is immobilized by the aldehyde-bisulfite adduct present in the developer scavenger layer. Any undesirable products formed in the developer-scavenger layer are masked from the viewer by the opaque light-reflective layer. If desired, the developer scavenger layer could also be located on the top transparent sheet. For further details concerning this particular integral film unit, its preparation and use, reference is made to the above-mentioned Cole U.S. application Ser. No. 027,990, filed Apr. 13, 1970.

In the photographic film units according to our invention, there is associated with each silver halide emulsion layer in the photosensitive element a dye image-providing material comprising a nondifiusible coupler which produces a diffusible dye on reaction with oxidized aromatic primary amino color developing agent in an alkaline processing composition.

The nondifiusible couplers employed in this invention include those having formulas:

DYE.'LINK COUPBAL'L) n and,

BALL---LINK-(COUPSOL) wherein (1) DYE is a dye precursor, e.g., a leuco dye, a shifted dye which shifts hypsochromically or bathochromically when subjected to a different environment such as a change in H, reaction with a material to form a complex, etc.; or a dye radical exhibiting selective absorption in the visible spectrum and containing an acidic solubilizing radical;

(2) LINK is a connecting radical such as an azo radical, a mercuri radical, an oxy radical, an alkylidene radical, a thio radical, a dithio radical or an azoxy radical;

(3) CO-UP is a coupler radical such as a S-pyrazolone coupler radical, a pyrazolotriazole coupler radical, a phenolic coupler radical or an open-chain ketomethylene coupler radical, COUP being substituted in the coupling position with LINK;

(4) BALL is a photographically inert organic ballasting radical of such molecular size and configuration as to render such coupler nondilfusible during development in the alkaline processing composition;

(5) SOL is a hydrogen atom or an acidic solubilizing group when the color developing agent contains an acidic solubilizing group, and SOL is an acidic solubilizing group when the color developing agent is free of an acidic solubilizing group; and

(6) n is an integer of l to 2 when LINK is an alkalidene radical, and n is 1 when LINK is an azo radical, a

radical or an azoXy radical.

The acidic solubilizing radicals attached to the diffusible dye producing couplers described above can be solubilizing radicals which when attached to the coupler or developer moieties of the dyes, render the dyes diffusible in alkaline processing compositions. Typical of such radicals are carboxylic, sulfonic, ionizable, sulfonamide, and hydroXy-substituted groups that lend to dyes negative charges.

The nature of the ballast groups in the ditfusible dyeproducing coupler compounds described above (BALL-) is not critical as long as they confer nondiffusibility to the coupler compounds. Typical ballast groups include long chain akyl radicals linked directly or indirectly to the coupler molecules as Well as aromatic radicals of the benzene and naphthalene series, etc., linked directly or indirectly to the coupler molecules by a splittable linkage, or by a removable or irremovable but otherwise nonfunctional linkage depending upon the nature of the coupler compound. Useful ballast groups have at least 8 carbon atoms.

Typical dye radical substituents (DYE-) include azo, azomethine, indoaniline, indophenol, anthraquinone and related dye radicals well known in the art that exhibit selective absorption in the visible spectrum. The dye radicals contain acidic solubilizing moieties.

"With regard to the above-described coupler radicals (COUP-), the coupling position is well known to those skilled in the photographic art. The S-pyrazolone coupler radicals couple at the carbon atom in the 4-position, the phenolic coupler radicals, including a-naphthols, couple at the carbon atom in the 4-position and the open-chain ketomethylene coupler radicals couple to the carbon atom forming the methylene moiety (e.g.,

*denoting the coupling position). Pyrazolotriazole couplers and their coupling position are described, for example, in U.S. Pat. 3,061,432 and U.S. application Ser. No. 778,329 of Bailey et al., filed Nov. 22, 1968.

Particularly good results are obtained when the cyanproducing coupler has the formula BALLO-CYAN- COUP, the magneta-producing coupler has the formula BALL=N NMAGCOUP or BALLS-MAGCOUP and the yellow-producing coupler has the formula BALLOYELLCO=UP wherein:

(a) BALL is a photographically inert organic ballasting radical having at least 8 carbon atoms and of such molecular size and configuration as to render the coupler nondiffusible during development in an alkaline processing composition;

(b) CYANCOUP is a phenolic coupler radical substituted in the 2-position with a fully substituted amido group and attached to the --O- moiety of the cyan-producing coupler in the coupling position;

(c) MAGCOUP is a 5-pyrazolone coupler radical joined to the -N=N or S moiety of the magneta-producing coupler in the coupling position; and

(d) YELLCO'UP is an open-chain ketomethylene coupler radical attached to the O moiety of the yellowproducing coupler in the coupling position;

The term nondilfusing used herein as applied to the couplers, has the meaning commonly applied to the term in color photography and denotes materials which for all practical purposes do not migrate or wander through organic colloid layers, such as gelatin, comprising the sensitive elements of the invention. The same meaning is to be attached to the term immobile.

The term diffusible as applied to the dyes formed from the nondiffusing couplers in this invention has the converse meaning and denotes materials having the property of diffusing effectively through the colloid layers of the sensitive elements in the presence of the nondiffusing, materials from which they are derived. Mobile has the same meaning.

When the couplers having the formula DYE-LINK (COUP-BALL) n as described above are reacted with oxidized color developing agent, the connecting radical (LINK) is split and a diffusible preformed dye (DYE) is released which diffuses imagewise to a reception layer. An acidic solubilizing group on the preformed dye lends diffusibility to the dye molecule. The coupling portion of the coupler (COUP) couples which the color developing agent oxidation product to form a dye that is nondiffusible because of the attached ballasting group (BALL) in a nonconpling position. In this type of coupler, the color of the diffusible dye is determined by the color of the preformed dye moiety (DYE), the color of the reaction product of color developer oxidation product and the coupler moiety (COUP) being unimportant to the color of the diffusible image.

When couplers having the formula as described above are reacted with oxidized color developing agent, the connecting radical (LINK) is split and a dilfusible dye is formed with the color developing agent oxidation product and the coupling portion (COUP) of the coupler which diffuses imagewise to a reception layer. Ditfusibility is imparted to the dye by an acidic solubilizing group attached to a noncoupling position of the coupling portion (COUP) of the coupler or to the color developing agent. The ballasting portion of the coupler remains immobile. In this type of coupler, the color of the diffusible dye is determined by the color of the reaction product of color developer oxidation product and the coupler moiety (COUP).

In using both types of couplers in the invention, the production of diifusible dye images is a function of the reduction of developable silver halide images which may involve direct or reversal development of the silver halide emulsions with an aromatic primary amino developing agent. If the silver halide emulsion employed is a direct positive silver halide emulsion, such as an internal image emulsion or a solarizing emulsion, which is developable in unexposed areas, a positive image can be obtained in the receiver portion of the film unit. In this embodiment, the nondiffusible coupler can be located in the silver halide emulsion itself. After exposure of the film unit, the alkaline processing composition permeates the various layers to initiate development of the exposed photosensitive silver halide emulsion layers. The aromatic primary amino color developing agent present in the film unit develops each of the silver halide emulsion layers in the unexposed areas (since the silver halide emulsions are direct positive ones), thus causing the developing agent to become oxidized imagewise corresponding to the unexposed areas of the direct positive silver halide emulsions layers. The oxidized developing agent then reacts with the nondiffusible coupler present in each silver halide emulsion layer to form imagew-ise distributions, respectively, of dilfusible cyan, magenta and yellow dye as a function of the imagewise exposure of each of the silver halide emulsion layers. At least a portion of the imagewise distributions of diffusible cyan, magenta and yellow dye diffuse to the image-receiving layer to provide a positive dye image. Specific examples of such nondiffusing couplers and other details concerning this type of photographic chemistry are found in US. Pats. 3,227,550 and 3,227,552.

Internal image silver halide emulsions useful in the above-described embodiment are direct positive emulsions that form latent images predominantly inside the silver halide grains, as distinguished from silver halide grains that form latent images predominantly on the surface thereof. Such internal image emulsions were described by Davey et al. in US. Pat. 2,592,250 issued Apr. 8, 1952, and elsewhere in the literature. Internal image silver halide emulsions can be defined in terms of the increased maximum density obtained When developed with internal-type developers over that obtained when developed with surface-type developers. Suitable internal image emulsions are those which, when measured according to normal photographic techniques by coating a test portion of the silver halide emulsion on a transparent support, exposing toa light intensity scale having a fixed time between 0.01 and 1 second, and developing for 3 minutes at 20 C. in Developer A below (internal-type developer), have a maximum density at least five times the maximum density obtained when an equally exposed silver halide emulsion is developed for 4 minutes at 20 C. in Developer B described below (surface-type developer). Preferably, the maximum density in Developer A is at least 0.5 density units greater than the maximum density in Developer B.

DEVELOPER A G. Hydroquinone 15 Monomethyl-p-aminophenol sulfate 15 Sodium sulfite (desiccated) '50 Potassium bromide 10 Sodium hydroxide 25 Sodium thiosulfate 20 Water to make one liter.

DEVELOPER B G. P-hydroxyphenylglycine 10 Sodium carbonate Water to make one liter.

The solarizing direct positive silver halide emulsions useful in the above-described embodiment are well known silver halide emulsions which have been effectively fogged either chemically or by radiation to a point which corresponds approximately to the maximum density of the reversal curve as shown by Mees, The Theory of the Photographic Process, published by the Macmillan Co., New York, N.Y., 1942, pp. 261297. Typical methods for the preparation of solarizing emulsions are shown by Groves British Pat. 443,245, Feb. 25, 1936, who subjected emulsions to Roentgen rays until an emulsion layer formed therefrom, when developed without preliminary exposure, is blackened up to the apex of its graduation curve; Szaz British Pat. 462,730, Mar. 15, 1937, the use of either light or chemicals such as silver nitrate, organic sulfur compounds and dyes to convert ordinary silver halide emulsions to solarizing direct positive emulsions; and Arens U.S. Pat. 2,005,837, June 25, 1935, the use of silver nitrate and other compounds in conjunction with heat to effect solarization. Kendall and Hill U.S. Pat. 2,541,472, Feb. 13, 1951, shows useful solarized emulsions particularly susceptible to exposure with longe wavelength light and initial development to produce the Herschel effect described by Mees above, produced by adding benzothiazoles and other compounds to the emulsions which are fogged either chemically or with white light. In using the emulsions a suflicient reversal image exposure is employed using minus blue light of from about 500-700 mg wavelength preferably 520-554 mg, to substantially destroy the latent image in the silver halide grains in the region of the image exposure. Particularly useful are the fogged direct positive emulsions of Berriman U.S. Pat. 3,367,778, Illingsworth U.S. Pats. 3,501,305; 3,501,306 and 3,501,507 and combinations thereof.

Internal image silver halide emulsions which contain or which processed in the presence of fogging or nucleating agents are particularly useful in the above-described embodiment employing nondiffusible couplers since the use of fogging agents is a convenient way to inject electrons into the silver halide grains. Suitable fogging agents include the hydrazines disclosed in Ives U.S. Pats. 2,588,982 issued Mar. 11, 1952 and 2,563,785 issued Aug. 7, 1951; the hydrazides and hydrazones disclosed in Whitmore U.S. Pat. 3,227,552 issued Jan. 4, 1966; hydrazone quaternary salts described in Lincoln and Heseltine application Ser. No. 828,064 filed Apr. 28, 1969; or mixtures thereof. The quantity of fogging agent employed can be widely varied depending upon the results desired. Generally, the concentration of fogging agent is from about 1 to about 20 mg. per square foot of photosensitive layer in the photosensitive element or from about 0.1 to about 2 grams per liter of developer if it is located in the developer. Other embodiments of our invention employ the photosensitive elements described in the above-mentioned U.S. Pats. 3,227,550; 3,227,551; 3,227,552; and in British Pat. 904,364, p. 19, lines 14l. These embodiments all employ the nondiffusible couplers described above.

Spectral sensitizing dyes can be used conveniently to confer additional sensitivity to the light sensitive silver halide emulsion of the multilayer photographic elements of the invention. For instance, additional spectral sensitization can be obtained by treating the emulsion with a solution of a sensitizing dye in an organic solvent or the dye may be added in the form of a dispersion as described in Owens et al. British Pat. 1,154,781. For optimum results, the dye can either be added to the emulsion as a final step or at some earlier stage.

Sensitizing dyes useful in sensitizing such emulsions are described, for example, in Brooker et al., U.S. Pat. 2,562,632, issued Oct. 24, 1950; Sprague U.S. Pat. 2,503,776, issued Apr. 11, 1950; Brooker et al. U.S. Pat. 2,493,748; and Taber et al. U.S. Pat. 3,384,486. Spectral sensitizers which can be used include the cyanines, merocyanines, complex (tri or tetranuclear) merocyanines, complex (tri or tetranuclear) cyanines, holopolar cyanines, styryls, hemicyanines (e.g. enamine hemicyanines), oxonols and hemioxonols. Dyes of the cyanine classes can contain such basic nuclei as the thiazolines, oxazolines, pyrrolines, pyridines, oxazoles, thiazoles, selenazoles and imidazoles. Such nuclei can contain alkyl, alkylene, hydroxyalkyl, sulfoalkyl, carboxyalkyl, aminoalkyl and enamine groups and can be fused to carbocyclic or heterocyclic ring systems either unsubstituted or substituted with halogen, phenyl, alkyl, haloalkyl, cyano, or alkoxy groups. The dyes can be symmetrical or unsymmetrical and can contain alkyl, phenyl, enamine or heterocyclic substituents on the methine or polymethine chain. The merocyanine dyes can contain the basic nuclei mentioned above as well as acid nuclei such as thiohydantoins, rhodanines, oxazolidenediones, thiazolidenediones, barbituric acids, thiazolineones, and malononitrile. These acid nuclei can be substituted with alkyl, alkylene, phenyl, carboxyalkyl, sulfoalkyl, hydroxyalkyl, alkoxyalkyl, alkylamino groups, or heterocyclic nuclei. Combinations of these dyes can be used, if desired. In addition, supersensitizing addenda which do not absorb visible light can be included, for instance, ascorbic acid derivatives, azaindenes, cadmium salts, and organic sulfonic acids as described in McF'all et al. U.S. Pat. 2,933,390 and Jones et al. US. Pat. 2,937,089.

The various silver halide emulsion layers of a color film assembly of the invention can be disposed in the usual order, i.e., the blue-sensitive silver halide emulsion layer first with respect to the exposure side, followed by the green-sensitive and red-sensitive silver halide emulsion layers. If desired, a yellow dye layer or a Carey Lea silver layer can be present between the blue-sensitive and greensensitive silver halide emulsion layer for absorbing or filtering blue radiation that may be transmitted through the blue-sensitive layer. *If desired, the selectively sensitized silver halide emulsion layers can be disposed in a different order, e.g., the blue-sensitive layer first with respect to the exposure side, followed by the red-sensitive and green-sensitive layers.

The silver halide emulsions used in this invention can comprise, for example, silver chloride, silver bromide, silver chlorobromide, silver bromoiodide, silver chlorobromoiodide or mixtures thereof. The emulsions can be coarse or fine grain and can be prepared by any of the well-known procedures, e.g., single jet emulsions, double jet emulsions, such as Lippmann emulsions, ammoniacal emulsions, thiocyanate or thioether ripened emulsions such as those described in Nietz et al. U.S. Pat. 2,222,264; Illingsworth U.S. Pat. 3,320,069; and McBride U.S. Pat. 3,271,157. Emulsions that contain silver halide grains having substantial surface sensitivity can be used, and emulsions that contain silver halide grains having substantial sensitivity inside the grains can be used such as those described in Davey et al. US. Pat. 2,592,250; Porter et al. U.S. Pat. 3,206,313; and Bacon et al. U.S. Pat. 3,447,927. The emulsions can be regular grain emulsions such as the type described in Klein and Moisar, J. Phot. Sci. volume 12, No. 5, Sept/Oct, 1964, pp. 242-251. Negative-type emulsions can be used or direct positive emulsions can be used such as those described in Leermakers U.S. Pat. 2,184,013; Kendall et al. U.S. Pat. 2,541,472; Berriman U.S. Pat. 3,367,778; Schouwenaars British Pat. 723,019; Illingsworth et al. French Pat. 1,520,821; Ives U.S. Pat. 2,563,785; Knott et al. U.S. Pat. 2,456,953 and Land U.S. Pat. 2,861,885.

The emulsions used in this invention can be sensitized with chemical sensitizers, such as with reducing agents; sulfur, selenium or tellurium compounds; gold, platinum or palladium compounds; or combinations of these. Suitable procedures are described in Sheppard et al. U.S. Pat. 1,623,499; Waller et al. U.S. Pat. 2,399,083; McVeigh U.S. Pat. 3,297,447; and Dunn U.S. Pat. 3,297,446.

The silver halide emulsions used in this invention may contain speed increasing compounds such as polyalkylene glycols, cationic surface active agents and thioethers or combinations of these as described in Piper U.S. Pat. 2,886,437; Dann et al. U.S. Pat. 3,046,134; Carroll et al. U.S. Pat. 2,944,900; and 'Gotfe U.S. Pat. 3,294,540.

The silver halide emulsions used in the practice of this invention can be protected against the production of fog and can be stabilized against loss of sensitivity during keeping. Suitable antifoggants and stabilizers each used alone or in combination include thiazolium salts described in Brooker et al. U.S. Pat. 2,131,038 and Allen et al. U.S. Pat. 2,694,716; the azaindenes described in Piper U.S. Pat. 2,886,437 and Heimbach et al. U.S. Pat. 2,444,- 605; the mercury salts as described in Allen et al. U.S. Pat. 2,728,663; the urazoles described in Anderson et al. U.S. Pat. 3,287,135; the sulfocatechols described in Kennard et al. U.S. Pat. 3,236,652; the oximes described in Carroll et al. British Patent 623,448; nitron; nitroindazoles; the mercaptotetrazoles described in Kendall et al. U.S. Pat. 2,403,927; Kennard et al. U.S. Pat. 3,266,897 and Luckey et al. U.S. Pat. 3,397,987; the polyvalent metal salts described in Jones U.S. Pat. 2,839,405; the thiuronium salts described in Herz et al. U.S. Pat. 3,220,839; and the palladium, platinum and gold salts described in Trivelli et al. U.S. Pat. 2,566,263 and Ytuzy et a1. U.S. Pat. 2,597,915; and the tetrazoles described in Hoppe U.S. Pat. 3,352,672.

In the above-described embodiments employing nondiffusible couplers, interlayers are generally employed between the various photosensitive color-forming units to scavenge oxidized developing agent and prevent it from forming an unwanted dye in another color-forming unit. Such interlayers would generally comprise a hydrophilic polymer such as gelatin and an immobilizing coupler, which is capable of reacting with oxidized aromatic primary amino color developing agent to form an immobile product.

As previously mentioned, the aromatic primary amino color developing agent employed in the above-described embodiments is preferably present in. the alkaline processing composition in the rupturable pod. The color developing agent can also be incorporated into the negative portion of the film unit as a separate layer, e.g., by employing a Schiff base derivative of an aromatic primary amino color developing agent such as that formed by reacting o-sulfobenzaldehyde and N,N-diethyl-3-methyl-4-aminoaniline. Such incorporated developing agent will be activated by the alkaline processing composition. While the incorporated developing agent can be positioned in any layer of the photosensitive element from which it can be readily made available for development upon activation with alkaline processing composition, it is generally either incorporated in the light-sensitive silver halide emulsion layers or in layers contiguous thereto. As mentioned above, aromatic primary amino color developing agents employed in this invention are preferably p-phenylenediamine developing agents. These developing agents are well known to those skilled in the art and include the following compounds and salts thereof:

4-amino-N,N-diethyl-S-methyl aniline, N,N-diethy1-p-phenylenediamine, N-ethyl-B-methane, sulfonamidoethyl-3-methyl-4- aminoaniline, 4-amino-N-ethyl-3 -methyl-N- (B-sulfoethyl) aniline, 4-amino-N-ethyl-3-methoxy-N- (,B-sulfoethyl) aniline, 4- amino-N-ethyl-N- fl-hydroxyethyl) aniline, 4-amino-N,N-diethyl-3-hydroxymethyl aniline, 4-amino-N-methyl-N- (,B-carboxyethyl) aniline, 4-amino-N,N-bis (,B-hydroxyethyl) aniline, 4-amino-N,N-bis(fi-hydroxyethyl)-3-methyl aniline, 3acetamido-4-amino-N,N-bis fl-hydroxyethyl) aniline, 4-amino-N-ethyl-N- (2,3-dihydroxypropyl) -3 -methyl aniline, 4-amino-N,N-diethyl-3- (3 -hydroxypropoxy) aniline, and the like.

The rupturable container employed in this invention can be of the type disclosed in U.S. Pat. Nos. 2,543,181; 2,643,886; 2,653,732; 2,723,051; 3,056,492; 3,056,491 and 3,152,515. In general, such containers comprise 3. rectangular sheet of fluid and air-impervious material folded longitudinally upon itself to form two walls which are sealed to one another along their longitudinal and end margins to form a cavity in which processing solution is contained.

In a color film unit according to the invention, each silver halide emulsion layer containing a dye imageproviding material or having the dye image-providing material present in a contiguous layer may be separated from the other silver halide emulsion layers in the negative portion of the film unit by materials in addition to those described above, including gelatin, calcium alginate, or any of those disclosed in U.S. Pat. No. 3,384,483, polymeric materials such as polyvinylamides as disclosed in U .3. Pat. 3,421,892, or any of those disclosed in French Pat. 2,028,236 or U.S. Pat. Nos. 2,992,104; 3,043,692; 3,044,873; 3,061,428; 3,069,263; 3,069,264; 3,121,011; and 3,427,158.

Generally speaking, except where noted otherwise, the silver halide emulsion layers in the invention comprise photosensitive silver halide dispersed in gelatin and are about 0.6 to 6 microns in thickness; the dye imageproviding materials are dispersed in an aqueous alkaline solution-permeable polymeric binder, such as gelatin, as a separate layer about 1 to 7 microns in thickness; and the alkaline solution-permeable polymeric intcrlayers, e.g., gelatin, are about 1 to 5 microns in thickness. Of course, these thicknesses are approximate only and can be modified according to the product desired. In addition to gelatin, other suitable hydrophilic materials include both naturally-occurring substances such as proteins, cellulose derivatives, polysaccharides such as dextran, gum arabic and the like; and synthetic polymeric substances such as water soluble polyvinyl compounds like poly(vinylpyrrolidone), acrylamide polymers and the like.

The photographic emulsion layers and other layers of a photographic element employed in the practice of this invention can also contain alone'or in combination with hydrophilic, water-permeable colloids, other synthetic polymeric compounds such as dispersed vinyl compounds such as in latex form and particularly those which increase the dimensional stability of the photographic mate rials. Suitable synthetic pqlymers include those described, for example, in Nottorf U.S. Pat. 3,142,568, issued July 28, 1964; White U.S. Pat. 3,193,386, issued July 6, 1965; Houc'k et al. U.S. Pat. 3,062,674; issued Nov. 6, 1962; Houck et al. U.S. Pat. 3,220,844, issued Nov. 30, 1965; Ream et a1. U.S. Pat. 3,287,289, issued Nov. 22, 1966; and Dykstra U.S. Pat. 3,411,911, issued Nov. 19, 1968. Particularly effective are Water-insoluble polymers of alkyl acrylates and methacrylates, acrylic acid, sulfoalkyl acrylates or methacarylate, those which have crosslinking sites which facilitate hardening or curing, and those which have recurring sulfobetaine units as described in D'ykstra Canadian Pat. 774,054.

Any material can be employed as the image-receiving layer in this invention as long as the desired function of mordanting or otherwise fixing the dye images will be obtained. The particular material chosen will, of course, depend upon the dye to be mordanted. If acid dyes are to be mordanted, the image-receiving layer can contain basic mordants such as polymers of amino guanidine derivatives of vinyl methyl ketone such as described in the Minsk U.S. Pat. 2,882,156 granted Apr. 14, 1959 and the polymers disclosed in copending U.S. application Ser. No. 100,491 of Cohen et al. filed Dec. 21, 1970. Other mordants useful in our invention include poly-4-vinyl pyridine metho-p-toluene sulfonate and similar compounds described in Sprague et al. US. Pat. 2,484,430 granted Oct. 111, 1949, and cetyl trimethylammonium bromide, etc. Eifective mordanting compositions are also described in Whitmore U.S. Pat. 3,271,148 and Bush U.S. Pat. 3,271,147.

Furthermore, the image-receiving layer can be sufficient by itself to mordant the dye as in the case of use of an alkaline solution-permeable polymeric layer such as N-methoxymethyl polyhexylmethylene adipamide; partially hydrolyzed polyvinyl acetate; polyvinyl alcohol with or without plasticizers; cellulose acetate; gelatin; and other materials of a similar nature. Generally, good results are obtained when the image-receiving layer, preferably alkaline solution-permeable, is transparent and about 0.25 to about 0.04 mil in thickness. This thickness, of course, can be modified depending upon the result desired. The image-receiving layer can also contain ultraviolet absorbing materials to protect the mordanted dye images from fading due to ultraviolet light brightening agents such as the stilbenes, coumarins, triazines, oxazoles, dye stabilizers such as the chromanols, alkylphenols, etc.

Use of a pH-lowering material in the dye image-receiving element of the invention will usually increase the stability of the transferred image. Generally, the pH- lowering material will eifect a reduction in the pH of the image layer from about 13 or 14 to at least 11 and preferably -8 within a short time after imbibition. For example, polymeric acids as disclosed in US. Pat. 3,362,819; or metallic salts, e.g. zinc acetate, zinc sulfate, magnesium acetate, the formates, acetates, propionates, stearates, nitrates or sulfates of zinc, aluminum, iron, maganese, cobalt or nickel, etc.; or solid acids as disclosed in US. Pat. 2,584,030 may be employed with good results. Such pH-lowering materials reduce the pH of the film unit after development to terminate development and substantially reduce further dye transfer and thus stabilize the dye image. The pH-lowering material can be present as a separate layer between the scavenger layer and the support or it can be contained in the scavenger layer if desired.

An inert timing or spacer layer can be employed in our invention between the developer scavenger layer and the dye image-receiving layer which times or controls the scavenging reaction as a function of the rate at which alkali diffuses through the inert spacer la'yer. Examples of such timing layers include gelatin, polyvinyl alcohol or any of those disclosed in US. Pat. 3,455,686. The timing layer is also effective in evening out the various reaction rates over a wide range of temperatures, e.g., premature pH reduction is prevented when imbibition is effected at temperatures above room temperature, for example, at '95 to 100 F. The timing layer is usually about 0.1 to about 0.7 mil in thickness. Especially good results are obtained when the timing layer comprises a hydrolyzable polymer or a mixture of such polymers which are slowly hydrolyzed by the processing composition. Examples of such hydrolyzable polymers include polyvinyl acetate, polyamides, cellulose esters, etc.

The alkaline processing composition employed in this invention is the conventional aqueous solution of an alkaline material, e.g., sodium hydroxide, sodium carbonate or an amine such as diethylamine, preferably possessing a pH in excess of 12, and preferably containing a developing agent as described previously. The solution also preferably contains a viscosity-increasing compound such as a high molecular weight polymer, e.g., a Water-soluble ether inert to alkaline solutions such as hydroxyethyl cellulose or alkali metal salts of carboxymethyl cellulose such as sodium carboxymethyl cellulose. A concentration of viscosity-increasing compound of about 1 to about 5% by weight of the processing composition is preferred which will impart thereto a viscosity of about 100 cps. to about 200,000 cps. In certain embodiments of our invention, an opacifying agent, e.g., TiO carbon black, etc. may be added to the processing composition.

While the alkaline processing composition used in this invention can be employed in a rupturable container, as described previously, to conveniently facilitate the introduction of processing composition into the film unit, other methods of inserting processing composition into the film unit could also be employed, e.g., interjecting processing solution with communicating members similar to hypodermic syringes which are attached either to a camera or camera cartridge.

The alkaline solution-permeable, substantially opaque, light-reflective layer employed in certain embodiments of photographic film units of our invention can generally comprise any opacifier dispersed in a binder as long as it has the desired properties. Particularly desirable are white light-reflective layers since they would be esthetically pleasing backgrounds on which to view a transferred dye image and would also possess the optical properties desired for reflection of incident radiation. Suitable opacifying agents include titanium dioxide, barium, sulfate, zinc oxide, barium stearate, silver flake, silicates, alumina, zirconium oxide, zirconium acetyl acetate, sodium zirconium sulfate, kaolin, mica, or mixtures thereof in widely varying amounts depending upon the degree of opacity desired. The opacifying agents may be dispersed in any binder such as an alkaline solution-permeable polymeric matrix such as, for example, gelatin, polyvinyl alcohol, and the like. Brightening agents such as the stilbenes, coumarins, triazines and oxazoles can also be added to the light-reflective layer, if desired. When it is desired to increase the opacifying capacity of the light-reflective layer, dark-colored opacifying agents may be added to it, e.g., carbon black, nigrosine dyes, etc.

The supports for the photographic elements of this invention can be any material as long as it does not deleteriously effect the photographic properties of the film unit and is dimensionally stable. Typical flexible sheet materials include cellulose nitrate film, cellulose acetate film, poly(vinyl acetal) film, polystyrene film, poly(ethyleneterephthalate) film, polycarbonate film, poly-a-olefins such as polyethylene and polypropylene film, and related films or resinous materials as well as glass. The support is usually about 2 to 6 mils in thickness.

While the invention has been described with reference to layers of silver halide emulsions and dye image-providing materials, dotwise coating, such as would be obtained using a gravure printing technique, could also be employed. In this technique, small dots of blue, green and red-sensitive emulsions have associated therewith, respectively, dots of yellow, magenta and cyan color-providing substances. After development, the transferred dyes would tend to fuse together into a continuous tone.

The photographic layers employed in the practice of this invention can contain surfactants such as saponin, anionic compounds such as the alkyl aryl sulfonates described in Baldsiefen U.S. Pat. 2,600,831; amphoteric compounds such as those described in Ben-Ezra US. Pat. 3,133,816; and water soluble adducts of glycidol and an alkyl phenol such as those described in Olin Mathieson British Pat. 1,022,878.

The various layers, including the photographic layers, employed in the practice of this invention can contain light absorbing materials and filter dyes such as those described in Sawdey US. Pat. 3,253,921; Gaspar US. Pat. 2,274,782; Silverstein et al. US. Pat. 2,527,583 and Van- Campen US. Pat. 2,956,879.

The sensitizing dyes and other addenda used in the practice of this invention can be added from water solutions or suitable organic solvent solutions can be used. The compounds can be added using various procedures including those described in Collins et al. US. Pat. 2,912,- 343; McCrossen et al. US. Pat. 3,342,605; Audran US. Pat. 2,996,287 and Johnson et al. US. Pat. 3,425,835.

The photographic layers used in the practice of this invention can be coated by various coating procedures including dip coating, air knife coating, curtain coating, or extrusion coating using hoppers of the type described in Beguin US. Pat. 2,681,294. If desired, two or more layers can be coated simultaneously by the procedures described in Russell US. Pat. 2,761,791 and Wynn British Pat. 837,095. This invention also can be used for silver halide layers coated by vacuum evaporation as described in British Pat. 968,453 and Lu Valle et al. US. Pat. 3,219,451.

The photographic and other hardenable layers used in the practice of this invention can be hardened by various organic or inorganic hardeners, alone or in combination, such as the aldehydes, and blocked aldehydes, ketones, carbocyclic and carbonic acid derivatives, sulfonate esters, sulfonyl halides and vinyl sulfonyl ethers, active halogen compounds, epoxy compounds, aziridines, active olefins, isocyanates, carbodiimides, mixed function hardeners and polymeric hardeners such as oxidized polysaccharides like dialdehyde starch and oxyguargum and the like.

The following examples further illustrate the invention.

15 16 EXAMPLE 1 G.

Potassium hydroxide 35 A multilayer, multicolor photosensitive element 1s prepared by coating the following layers in the order recited 4 N ethyl'N'p'hydroxyethylamhne sulfate 40 on an opaque cellulose acetate film support: f d t 020 (1) Red-sensitive internal image gelatin-silver chloro- 5 g 3 reluc one bromide emulsion (130 mg. gelatin/ft. and 110 mg. i s y gi h e silver/ft. cyan image transfer coupler 1-hydr0Xy-4- yce i 001 {4 [a (3-pentadecylphenoxy)butyramido]phen0xy}-N- 'P S g g 85 6 ethyl-3',5'-dicarboxy-Z-naphthanilide 12o Ing./ft. and e W er 0 a fogging agent formyl-4-methylphenylhydrazine (0.5 g./ After 60 seconds at about 24 C./50% RH, the film units mole of silver chlorobromide) are separated. The minimum densities to red, green and (2) A scavenger interlayer comprising 1-hydroxy-N- blue light are measured both fresh and incubated for 48 [a (2,4-di-tert-amylphenoxy)butyl1-2-naphthamide (45 hours at 60 C./ 70% RH and 4 days at 38 C./ 88% mg./ft. tri-cresyl phosphate (23 mg./ft. and gelatin RH/ 1800 foot-candles of fluorescent light. The following (65 mg./ft. sensitometric results are obtained:

Minimum densities Fresh 48 hrs. 4 days 2 Developer scavenger R G B R G B R G B Nonecontrol 0.30 0.42 0.36 2.44 2.31 2.18 Sodium formaldehyde bisulfite adduct 0.20 0.21 0.30 0.14 0.22 0.34 0.16 0.21 0.38

1 60 C./70% RH.

2 38 C./88% RH 1,800 ft.-eaudles fluorescent light.

3 66 hrS./60 C./70% RH.

(3) Green-sensitive internal image gelatin-silver chlorobromide emulsion (116 mg. gelatin/ft. and 100 mg. silver/ft. magenta image transfer coupler 1-phenyl-3- [(3,5 dicarboxyanilino) octadecylcarbamylphenylthio]- S-pyrazolone (80 mg./ft. diethyl lauramide (40 mg./ ft?) and a fogging agent formyl-4-methy1phenylhydrazine (0.5 g./mole of silver chlorobromide) (4) A scavenger and a yellow filter layer comprising 1 hydroxy N [a (2,4-di-tert-amylphenoxy)butyl]-2- naphthamide (50 mg./ft. tri-cresyl phosphate mg./ ft. yellow Carey Lea silver (15 mg./ft. and gelatin (65 mg./ft.

(5) Blue-sensitive internal image gelatin-silver chlorobromoiodide emulsion (126 mg. gelatin/ft. and 100 mg. silVer/ft. yellow image transfer coupler ot-PiV3lY1-oc-[4- (N-methlyl-N-n-octadecylsulfamyl)-phenoxy] 4 sulfo acetanilide, potassium salt (70 mg./ft. and fogging agent formyl-4-methylphenylhydrazine (0.5 g./mole of silver chlorobromide).

(6) Overcoat of gelatin (50 mg./ft. and l-hydroxy- N-[ot-(2,4-di-tert-amylphenoxy)butyl] 2 naphthamide (2O mg./ft.

A multilayer dye image-receiving element is prepared by coating the following layers in the order recited on a paper support:

(1) a combined developer-scavenging and pH-lowering layer comprising zinc sulfate (500 mg. /ft. sodium formaldehyde bisulfite adduct (1 00 mg./ft. and terpoly (methyl acrylate/3-acryloyloxypropane-l-sulfonic acid, sodium salt/2-acetoacetoxyethyl methacrylate) (7 :4:0.25) (2000 mg./ft.

(2) a timing layer of 50% hydrolyzed poly(vinyl acetate) (500 mg./ft. and

(3) an image-receiving layer of copoly[styrene-N-benzyl N,N dimethyl N-(3-maleimidopropyl)ammonium chloride] (200 rug/ft?) and poly(vinyl alcohol) (200 mg./ft.

A control dye image-receiving element is prepared but without the aldehyde bisulfite developer scavenger material.

Two samples of the photosensitive element are exposed to a graduated-density multicolor test object. The following processing composition is employed in a pod and is spread between the exposed surface of the photosensitive element and each superposed dye image-receiving element by passing the transfer sandwich between a pair of puxtaposed pressure rollers:

The above results indicate that the dye image-receiving element which contains the aldehyde bisulfite addition product prevents stain due to unused color developing agent in the receiving element. This protection is obtained initially and is maintained throughout accelerated keeping tests.

EXAMPLE 2 This example illustrates the use of a light-reflective material in a dye image-receiving element according to our invention.

A multilayer dye imagereceiving element is prepared by coating the following layers in the order recited on a paper support:

(1) a combined developer-scavenging and pH-lowering layer comprising zinc sulfate (250 mg. ft?) sodium formaldehyde bisulfite adduct (1000 mg./ft. and terpoly (N-isopropylacrylamide/3-acryloyloxypropane-l sulfonic acid, sodium salt/2 acetoacetoxyethyl methacrylate) (7:4:0.25) (2000 mg./ft.

(2) a combined light-reflective layer and timing layer comprising 50% hydrolyzed poly(vinyl acetate) (500 mg./ft. and titanium dioxide (1000 mg./ft. and

(3) an image-receiving layer of copoly[styrene-N-benzyl N,N dimethyl-N-(3-maleimidopropyl) ammonium chloride] (200 mg./ft. and poly(vinyl alcohol) (200 mg./ft.

A control dye image-receiving element is prepared but without the aldehyde bisulfite developer scavenger material.

Two samples of the photosensitive element of Example 1 are exposed and processed with the above receiving elements as in Example 1. The minimum densities to red, green and blue light are measured both fresh and incubated for 66 hours at 60/70% RH. The following sensitometric results are obtained:

Minimum densities The above results demonstrate the effectiveness in employing aldehyde bisulfite addition products according to the invention in combination with a light-reflective material.

1 7 EXAMPLES 3-5 Example 1 is repeated except that sodium acetaldehyde bisulfite adduct, bis(sodium succinaldehyde bisulfite)adduct and bis(sodium glutaraldehyde bisulfite) are substituted at the same concentration for sodium formaldehyde bisulfite adduct. Similar results are obtained.

EXAMPLE 6 An integral multilayer photosensitive element is prepared by coating the following layers in the order recited on a transparent cellulose acetate film support:

(1) Image receiving layer of N-n-octadecyl-tributylammonium bromide (200 mg./ft. di-n-butyl-phthalate (200 mg./ft. and gelatin (700 mg./ft.

(2.) Interlayer of gelatin (100 mg./ft.

(3) Light reflecting layer of TiO (2000 mg./ft. and gelatin (200 mg./ft.

(4) Opaque Scavenger Interlayer of l-hydroxy-N-[a- (2,4-di-tert-amylphenoxy)butyl]-2-naphthamide (20 mg./ 2L2), gelatin (200 mg./ft. and carbon black (250 mg./

(5) Red-sensitive internal image gelatin-silver chlorobromide emulsion (88 mg. gelatin/ft. and 100 mg. silver/ ftfi), cyan image transfer coupler 1-hydroxy-4-{4-[u-(3- pentadecylphenoxy)butyramido]-phenoxy}-N-ethyl 3,5- dicarboxy-2naphthanilide (70 mg./ft. and fogging agent formyl 4-methylphenylhydrazine (1.0 g./mole of silver chlorobromide) (6) Scavenger Interlayer of 1 hydroxy-N-[u-(2,4-ditert-amylphenoxy)butyl] 2-naphthamide (65 mg./ft. tricresylphosphate (23 mg./ft. and gelatin (80 mg./ft.).

(7) Green-sensitive internal image gelatin-silver chlorobromide emulsion (104 mg. gelatin/ft. and 100 mg. silver/ft. magenta image transfer coupler 1-phenyl-3- [(3,5 dicarboxyanilino)octadecylcarbamoylphenylthio]- S-pyrazolone (70 rug/ft?) and fogging agent formyl-4- methylphenylhydrazine (1.0 g./mole of silver chlorobromide).

(8) Scavenger and yellow filter layer of l-hydroxy-N- [a (2,4-di-tert-amy1phenoxy)butyl]-2-naphthamide (65 mg./ft. tri-cresyl phosphate (25 mg./ft. and Carey Lea Silver (15 mg./ft.

(9) Blue-sensitive internal image gelatin-silver chlorobromide emulsion (109 mg. gelatin/ft. and 100 mg. silver/ft yellow image transfer coupler a-pivalyl-u-(3- pentadecyl 4-nitrophenoxy)-4-sulfamyl-acetamlide (90 mg./ft. and fogging agent formyl-4-methylphenylhydrazine (1.0 g./mole of silver chlorobromide).

(10) Overcoat layer of gelatin (50 mg./ft. A sample of the element is exposed to a graduated-density multicolor test object. The following processing composition is employed in the processing pod:

G. Piperidinohexose reductone 0.2 S-Methylbenzimidazole 0.05 Potassium hydroxide 35.0 4-Amino-N-ethyl-N-p-hydroxyethylanilinosulfate 40.0 Hydroxyethylcellulose 30.0

Distilled water to 1 liter.

The processing solution is spread from the pod between the exposed surface of the element and an opaque cellulose acetate film support coated with (1) a layer comprising completely hydrolyzed copoly (methylvinyl ether/ maleic anhydride) (1450 mg./ft. acetic anhydride (410 mg./ft. and 1-phenyl-S-mercaptotetrazole (10 mg./ft.), and (2) a cellulose acetate (85 mg./ft. timing layer by passing the transfer sandwich between a pair of juxtaposed pressure rollers. After one minute at about 20 C., a multicolor reproduction of the test object is observed on a white background when viewed through the transparent film support side of the element. After two days, the minimum density of the images to red, green and blue light is measured and recorded in the table.

18 EXAMPLE 7 Example 6 is repeated except layer (1) of the opaque process sheet also contains sodium formaldehyde bisulfite adduct (536 mg./ft.

EXAMPLE 8 Example 6 is repeated except that the opaque process sheet comprises an opaque cellulose acetate film support coated with (1) a layer comprising gelatin 1250 mg./ft. sodium dihydrogen phosphate (1104 mg./ft. and l-phenyl-S-mercaptotetrazole (50 mg./ft. and (2) a cellulose acetate mg./ft. timing layer.

EXAMPLE 9 Example 8 is repeated except that layer 1) of the opaque process sheet also contains sodium formaldehyde bisulfite adduct (536 mg./ft.

TABLE Minimum densities Developer Example scavenger Red Green Blue 1 Sodium formaldehyde bisulfite adduct. 3 N o distinguishable image remains after two days.

As will be seen by comparing the results of Example 6 with Example 7 and Example 8 with Example 9, the use of an aldehyde bisulfite addition product in an integral photosensitive element significantly improves the stability of the transfer image upon keeping.

EXAMPLES 10-11 Examples 6-9 are repeated except that the process sheet is transparent, the processing composition contains carbon (20 g.), the film unit is preassembled with the process sheet superposed over the photosensitive element prior to exposure which takes place through the process sheet, and the pod is positioned adjacent the photosensitive element and process sheet. Results similar to those of Examples 6-9 are obtained.

The invention has been described in detail with particular reference to preferred embodiments thereof, but, it will be understood that variations and modifications can be aflected within the spirit and scope of the invention.

We claim:

1. In a photographic film unit which is adapted to be processed by passing said unit between a pair of juxtaposed pressure-applying members comprising:

'(a) a photosensitive element comprising a support hav ing thereon at least one photosensitive silver halide emulsion layer, each said silver halide emulsion layer having associated therewith a nondifiusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a dilfusible dye;

(b) a dye image-receiving layer; and

(c) a rupturable container containing an alkaline processing composition and which is adapted to be positioned during processing of said film unit so that a compressive force applied to said container by said pressure-applying members will effect a discharge of the containers contents Within said film unit;

said film unit containing an aromatic primary amino color developing agent; the improvement comprising employing in said film unit a developing agent scavenger layer comprising an aldehyde-bisulfite addition product in a polymeric binder. I

2. The film unit of claim 1 wherein said photosensitive element comprises a support having thereon a red-sensitive silver halide emulsion layer having associated therewith a cyan dye image-providing material comprising a non-diifusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a diifusible cyan dye, a green-sensitive silver halide emulsion layer having associated therewith a magenta dye image-providing material comprising a non-difiusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a diffusible magenta dye, and a blue-sensitive silver halide emulsion layer having associated therewith a yellow dye image-providing material comprising a nondiffusible coupler capable of reacting with oxidized amino color developing agent to produce a diffusible yellow dye.

3. The film unit of claim 2 wherein said dye imagereceiving layer is located in said photosensitive element between said support and the lowermost photosensitive silver halide emulsion layer.

4. The film unit of claim 3 wherein said support is transparent, said film unit also includes a transparent sheet superposed over the layer outermost from said transparent support of said photosensitive element, and said rupturable container also contains an opacifying agent and is positioned transverse a leading edge of said photosensitive element so that a compressive force applied to said container will effect a discharge of the containers contents between said transparent sheet and the outermost layer of said photosensitive element.

5. The film unit of claim 4 wherein said scavenger layer is located in said photosensitive element between said dye image-receiving layer and said lowermost photosensitive silver halide emulsion layer.

6. The film unit of claim 3 wherein said support is transparent, said film unit also includes a substantially opaque process sheet adapted to be superposed over the layer outermost from the transparent support of said photosensitive element, and said rupturable container is adapted to be positioned during processing of said film unit so that a compressive force applied to said container will efiect a discharge of the containers contents between said process sheet and the outermost layer of said photosensitive element.

7. The film unit of claim 6 wherein said scavenger layer is located in said photosensitive element between said dye image-receiving layer and said lowermost photosensitive silver halide emulsion layer.

8. The film unit of claim 2 wherein said dye imagereceiving layer is coated on a separate support and is adapted to be superposed on said photosensitive element after exposure thereof.

9. The film unit of claim 8 wherein said scavenger layer is located between said dye image-receiving layer and its said support.

10. The film unit of claim 8 wherein said rupturable container is so positioned during processing of said film unit that a compressive force applied to said container by said pressure-applying members will effect a discharge of the containers contents between said dye image-receiving layer and the outermost layer of said photosensitive element.

11. The film unit of claim 9 which contains a timing layer between said scavenger layer and said dye imagereceiving layer.

12. The film unit of claim 11 wherein said timing layer also contains a light-reflective material.

13. The film unit of claim 8 which also contains a pH-lowering material.

14. The film unit of claim 1 wherein said aldehydebisulfite addition product has the formula:

R-CHSO M or .(II) OH OH or polymers and copolymers having recurring units of the following formula:

(III) R wherein R represents a hydrogen atom or an alkyl n represents an integer of from 1 to 6; and

M represents an alkali metal ion.

15. The film unit of claim 1 wherein said aldehyde bisulfite adduct is soduim formaldehyde bisulfite adduct, sodium acetaldehyde bisulfite adduct, bis(sodium succinaldehyde bisulfite)adduct, bis(sodium glutaraldehyde bisulfite) adduct, or combinations thereof.

16. In a photographic film unit which is adapted to be processed by passing said unit between a pair of juxtaposed pressure-applying members comprising:

(I) a photosensitive element comprising a support having thereon the following layers in sequence:

(a) a direct positive, red-sensitive silver halide emulsion layer containing a nondiffusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a diffusible cyan dye;

(b) an alkaline solution-permeable interlayer containing a compound capable of scavenging oxidized aromatic primary amino color developing agent;

(c) a direct positive, green-sensitive silver halide emulsion layer containing a nondiifusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a difiusible magenta dye;

(d) an alkaline solution-permeable interlayer containing a compound capable of scavenging oxidized aromatic primary amino color developing agent; and

(e) a direct positive, blue-sensitive silver halide emulsion layer containing a nondilfusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a difi'usible yellow dye; each said nondiffusible coupler having the formula DYELINK(COUPBALL) n BALLLINK(COUPSOL) wherein:

(1) DYE is a dye precursor or a dye radical exhibiting selective absorption in the visible spectrum and containing an acidic solubilizing group;

(2) LINK is a connecting radical selected from the group consisting of an azo radical, a mercuri radical, an oxy radical, an alkylidene radicals, a thio radical, a dithio radical and an azoxy radical;

(3) COUP is a coupler radical selected from the group consisting of a S-pyrazolone coupler radical, a pyrazolotriazole coupler radical, a phenolic coupler radical and an open-chain ketomethylene coupler radical, said COUP being substituted in the coupling position with said LINK;

(4) BALL is a photographically inert organic ballasting radical of such molecular size and configuration as to render said coupler nondigusible during development in said alkaline processing composition;

(5) SOL is selected from the group consisting of a hydrogen atom and an acidic solubilizing group when said color developing agent contains an acidic solubilizing group, and SOL is an acidic solubilizing group 21 when said color developing agent is free of an acidic solubilizing group;

(6) n is an integer of 1 to 2 when said LINK is an alkylidene radical, and n is 1 when said LINK is a radical selected from the group consisting of an azo radical, a mercuri radical, an oxy radical, a thio radical, a thio radical, a dithio radical and an azoxy radical;

(II) a dye image-receiving element comprising a support having thereon a dye image receiving layer, said element being adapted to be superposed over said blue-sensitive silver halide emulsion layer after exposure of said photosensitive element; and

(III) a rupturable container containing an alkaline processing composition and which is adapted to be positioned during processing of said film unit so that a compressive force applied to said container by said pressure-applying members will effect a discharge of the containers contents between said dye imagereceiving layer and said blue-sensitive silver halide emulsion layer of said photosensitive element;

said film unit containing an aromatic primary amino color developing agent; the improvement comprising employing between said dye image-receiving layer and its said support a developing agent scavenger layer comprising an aldehyde-busufite addition product in a polymeric binder.

17. A dye image-receiving element adapted to be superposed on a photosensitive element after exposure thereof comprising a support having thereon the following layers in the order recited:

(a) a developing agent scavenger layer comprising an aldehydebisulfite addition product in a polymeric binder, and

(b) a dye image-receiving layer.

18. The dye image-receiving element of claim 17 which contains a timing layer between said scavenger layer and said dye-image-receiving layer.

19. The dye image-receiving element of claim 18 wherein said timing layer also contains a light-reflective material.

20. The dye image-receiving element of claim 17 which also contains a pH-lowering material.

21. The dye image-receiving element of claim 20 wherein said pH-lowering material is contained in said scavenger layer.

22. The dye image-receiving element of claim 17 wherein said aldehyde-bisulfite addition product has the formula:

or polymers and copolymers having recurring units of the following formula:

(III) R -CHg(B- HO H-SOzM wherein R represents a hydrogen atom or an alkyl group;

22 sensitive silver halide emulsion layer, each said silver halide emulsion layer having associated therewith a nonditfusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a ditfusible dye;

(B) treating the layer outermost from the support of said photosensitive element with an alkaline processing composition to effect development of each of said exposed silver halide emulsion layers with an aromatic primary amino color developing agent,

(C) forming an imagewise distribution of diffusible dye image-providing material as a function of said imagewise exposure of each said silver halide emulsion layer; and

(D) at least a portion of each said imagewise distributions of ditfusible dye image-providing material diffusing to a dye image-receiving layer;

the improvement comprising employing in said photosensitive element or adjacent to said dye image-receiving layer a developing agent scavenger layer comprising an aldehyde-bisulfite addition product in a polymeric binder.

25. The process of claim 24 wherein said treatment step (B) is effected by (a) superposing over the layer outermost from the support of said photosensitive element said dye imagereceiving layer coated on a support; said scavenger layer being located between said dye image-receiving layer and its said support;

(b) positioning a rupturable container containing said alkaline processing composition between said exposed photosensitive element and said dye imagereceiving layer; and

(c) applying a compressive force to said container to effect a discharge of the containers contents between said outermost layer of said exposed photosensitive element and said dye image-receiving layer.

26. The process of claim 25 wherein said aldehydebisulfite addition product has the formula:

(II) OH OH I MOaS-CH-(CHzMH-SOsM or polymers and copolymers having recurring units of the following formula:

( -oH, o-

HO- H-S 03M References Cited UNITED STATES PATENTS 3,424,583 1/1969 'Seiter et al. 96-74 NORMAN G. TOROHIN, Primary Examiner A. T. SURA PICO, Assistant Examiner US. Cl. X.R. 96-29 D, 56