US3770431A - Photographic elements containing ballasted resorcinols - Google Patents

Photographic elements containing ballasted resorcinols Download PDF

Info

Publication number
US3770431A
US3770431A US00181262A US3770431DA US3770431A US 3770431 A US3770431 A US 3770431A US 00181262 A US00181262 A US 00181262A US 3770431D A US3770431D A US 3770431DA US 3770431 A US3770431 A US 3770431A
Authority
US
United States
Prior art keywords
layer
ballasted
silver halide
halide emulsion
photographic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US00181262A
Other languages
English (en)
Inventor
J Gates
I Salminen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Application granted granted Critical
Publication of US3770431A publication Critical patent/US3770431A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/392Additives
    • G03C7/39208Organic compounds
    • G03C7/39212Carbocyclic
    • G03C7/39216Carbocyclic with OH groups
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/35Antiplumming agents, i.e. antibronzing agents; Toners
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C8/00Diffusion transfer processes or agents therefor; Photosensitive materials for such processes

Definitions

  • This invention relates to photographic elements and processes of forming images in photographic elements.
  • this invention relates to photographic elements containing a ballasted resorcinol compound.
  • this invention relates to photographic elements which have improved resistance to environmental effects, background stain, etc.
  • this invention relates to improved image transfer systems.
  • additives used as scavengers acted as a redox agent, especially in the case of scavenging oxidized developers, and reduced the oxidized developing agent.
  • antistain agents were silver halide developers which could enter in competing reactions with color developing agents. Therefore, improved additives are desirable, especially in color systems such as image transfer systems.
  • ballasted resorcinol compounds can be used in photographic elements to improve the image quality and aging properties of the image record.
  • the photographic elements of this invention comprise a'compound of the formula:
  • the photographic elements containing the above ballasted resorcinol compounds have improved image I properties; apparently, these compounds are very effective as'scavengers for by-products or excess ingredithus, can be put in any desired layer of the photo-' graphic element since they will not compete with the developing agents or reactivate oxidized developing agents.
  • ballasted resorcinol compounds can generally be incorporated in hydrophilic colloid layers with organic solvents having low boiling points, such as acetone, ethyl acetate, etc.; thus thinner coatings can be used compared to couplers requiring large amounts of high-boiling-point organic solvents to achieve uniform dispersion.
  • the ballasted resorcinols are present in a photographic element which is processed with a color developing agent.
  • the ballasted resorcinols are present in photographic elements in combination with color-forming couplers to scavenge oxidized color developer which does not react with the color coupler.
  • the scavengers of this inven-' tion are used in combinationwith a timing means so that development in the photosensitive element is substantially complete before the scavenger is effectively associated with the development medium.
  • the scavengers of this invention are used in combination with color transfer units, and preferably those transfer units wherein the dye image-receiving layer is integral with the photosensitive element itself or is .provided on a separate support ents in silver halide development reactions, especially color development reactions, When -color developers such as aromaticprimary amines are used in the development reaction, the ballasted resorcinols appear to scavenge the excess developer which may provide discoloration upon aerial oxidation or extraneous oxidato be superposed on the photosensitive element after exposure thereof.
  • -elements of this type comprise a film unit which is adapted to be processecl 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:' 0' I i 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 3 image-providing material comprising a nondiffusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a diffusible dye;
  • a rupturable container containing an alkaline 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 a ballasted resorcinol in a polymeric binder which is capable of reacting with unused aromatic primary amino color developing agent to form a colorless or substantially colorless reaction product.
  • ballasted resorcinols of this invention generally require the use of an organic solvent to achieve a uniform dispersion in a hydrophilic colloid layerof a photographic element.
  • organic solvents having a boiling point of less than 100 C., such as acetone, ethyl acetate and the like, are very effective in achieving uniform dispersions of the present scavengers.
  • high-boiling-point organic solvents such as coupler solvents, can be used to obtain dispersions, they are generally not employed since it is usually more practical to use low-boiling-point solvents.
  • the ballasted resorcinols can generally be incorporated in photographic elements by any of the techniques employed in the art for dispersing materials of this type which have very marginal water solubility. When they are dispersed in hydrophilic colloid layers they can be dispersed by techniques known for dispersing coupler solvents or by means employing the low-boiling-point solvents to obtain uniform dispersions.
  • the ballasted resorcinols can be employed in any concentration useful for the intended purpose. However, generally lower weight percentages of the present ballasted resorcinols are required to provide an effective scavenging as compared to other compounds used in the prior art for this purpose. We have found that concentrations of from 1 mg. per square foot to about 500 mg. per square foot, and preferably from about5 mg. to 100 mg. per square foot, can be used for most purposes.
  • the ballasted resorcinols'can generally be located in any layer of a photographic element (including imagereceiving. sheets).
  • the ballasted resorcinols can generally be incorporated in all vehicles used in coating photographic elements including, for example, proteins, cellulose derivatives, polysaccharides, synthetic polymeric substances and the like.
  • the ballasted resorcinols are incorporated in hydrophilic, water-permeable colloids, or synthetic polymeric compounds such as dispersed vinyl compounds such as in latex form and particularly those which'increase the dimensional stability of the photographic materials.
  • Suitable synthetic polymers include those described, for example, in US. Pat. Nos.
  • nondiffusing used herein 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.
  • diffusible has the converse meaning and denotes materials having the property of diffusing effectively through the colloid layers of the photographic elements, and generally refers to materials which can migrate to any layer of the element during aqueous treatment.
  • Mobile has the same meaning.
  • the scavengers of this invention can be used in any photographic element where it is desired to immobilize or scavenge an unwanted reaction product or contaminant. In one embodiment, they are used effectively in black-and-white or color photographic products to scavenge unwanted aldehydes. in another embodiment, the ballasted resorcinols are especially useful in color photographic elements which employ a color silver halide developer during processing.
  • color developer is understood to refer to that class of compounds known in the art as color silver halide developers, and generally refers to silver halide developers which in their oxidized form will couple with a color-forming coupler. Generally, these developers are aryl compounds having at least one NH group thereon.
  • the ballasted resorcinols are used in image transfer systems including those transfer systems wherein the image-receiving layer remains integral with the photosensitive emulsion, as well as those where the imagereceiving layer is separated from the photosensitive layers.
  • the novel dye image-receiving element comprises a support having thereon the following layers:
  • a scavenger layer comprising a ballasted resorcinol in a polymeric binder and b. a dye image-receiving layer.
  • a timing layer can also be em- I ployed in the invention between the scavenging layer and the dye image-receiving layer which functions to delay the rate of diffusion of aromatic primary amino color developing agent into the scavenging layer.
  • the timing layer therefore, ensures the efficient use of the aromatic primary amino color developing agent in the photosensitive element prior to scavenging action by the ballasted resorcinol.
  • 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 imagereceiving layer or can be combined with the timing layer if one is employed.
  • the image dyes formed in the respective blue-, greenand redsensitive 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 diffusion 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.
  • the 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.
  • integral receiver-negative photosensitive elements are described in copending U.S. application Ser. No. 115,459 of Barr, Bush and Thomas filed Feb. 16, 1971, now abandoned.
  • 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 scavenger layer comprising a ballasted resorcinol dispersed in a suitable binder, and the various layers forming the color-forming units.
  • 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 image-receiving layer to provide a positive, rightreading image which is viewed through the transparent support on the opaque reflecting layer background. It is believed that positioning of the scavenger layer between the color-forming photosensitive units and the image-receiving layer in the integral receiver-negative film system prevents the diffusion of unused color developer into the image-receiving layer. If desired, an auxiliary scavengerlayer comprising the scavenging materials described herein can be located on the opaque process sheet. For further detailsconcerning this particular integral film unit, its preparation and use, reference is made to the above-mentioned U.S. ap-
  • the support for the color diffusion transfer system is transparent and is coated with the imagereceiving layer, a substantially opaque, light-reflective layer, e.g., ,TiO a scavenger layer comprising a ballasted resorcinol 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 pressure-applying members in the camera as it is being removed therefrom.
  • the pressureapplying members rupture the container and spread processing composition and opacifier over the negative portion of the film 'unit to render it lightfinsensitive.
  • 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 a 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 difiuse in the direction of the image-receiving layer is immobilized by the ballasted resorcinol present in the scavenger layer.
  • ballasted resorcinols are used in the photographic film units where there is associated with each silver halide emulsion layer in the photosensitive element a dye imageproviding material comprising a nondiffusible coupler which produces a diffusable dye on reaction with oxidized aromatic primary amino color developing agent in an alkaline processing composition.
  • timing or spacer layers referred to above can be employed in photographic elements of our invention. Generally, they are employed between the scavenger layer and a 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 layer.
  • timing layers include gelatin, polyvinyl alcohol or any of those disclosed in U.S. Pat. No. 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.
  • the timing layer comprises a hydrolyzable polymer or a mixture of such polymers which are slowly hydrolyzed by the processing composition.
  • hydrolyzable polymers include polyvinyl acetate, polyamides, cellulose esters, etc.
  • the light-sensitive element A is exposed through the support of element A to a graduateddensity test object and presoaked for 5 seconds at a temperature of 70 F. in the processing solution.
  • the receiver B is presoaked for seconds in the same solution and subsequently brought into contact with the light-sensitive element. Both are passed between rubber rollers and left in contact for 3 minutes.
  • the receiver is analyzed for silver in the areas corresponding to minimum exposure of the negative. Cyan dye density developed in the receiver and the level of silver found in the receiver are both indications of the efficiency of consumption of oxidized developer by the nucleated layer (layer 3) of the negative.
  • the compounds are dissolved in 2,4-di-namylphenol, as disclosed in US. Pat. No. 2,835,579, and then incorporated in the coating composition prior to coating.
  • a photographic element comprising a supporlg at' .least one layer thereon being an image-receiving layer or containing a silver halide emulsion, and at least one layer thereon containing an immobile, ballasted resorcinol compound.
  • said photographic element comprises at least one layer containing a silver halide emulsion.
  • ballasted resorcinol compound is represented by the formula:
  • Ball represents a ballast group containing at least eight carbon atoms.
  • ballasted resorcinol is 5-npentadecylresorcinol.
  • ballasted resorcinol is S-n-pentadecylenecarbon-amidoresorcinol.
  • a photographic element according to claim 1 which comprises at least one layer containing a silver halide emulsion having associated therewith a photographic color coupler.
  • a photographic film unit which is adapted to be processed by passing said unit between a pair of juxtaposed pressure-applying members comprising:
  • a photosensitive element comprising a support having thereon at least one photosensitive silver halide emulsion layer, each said silver halide emulsion layer having associated therewith a nondiffusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a diffusible dye;
  • said film unit containing an aromatic amino color developing agent; the improvement comprising employ- -ing a developing agent scavenger layer comprising a ballasted resorcinol in a polymeric binder.
  • the film unit of claim 10 which contains a timing layer between said scavenger layer and said dye imagereceiving layer.
  • a transfer image comprising a. imagewise-exposing a photosensitive element comprising a support having thereon at least one photosensitive silver halide emulsion layer, each said silver halide emulsion layer having associated therewith a nondif-fusible coupler capable of reacting with oxidized aromatic primary amino color developing agent to produce a diffusible dye;

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Color Printing (AREA)
US00181262A 1971-09-16 1971-09-16 Photographic elements containing ballasted resorcinols Expired - Lifetime US3770431A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US18126271A 1971-09-16 1971-09-16

Publications (1)

Publication Number Publication Date
US3770431A true US3770431A (en) 1973-11-06

Family

ID=22663531

Family Applications (1)

Application Number Title Priority Date Filing Date
US00181262A Expired - Lifetime US3770431A (en) 1971-09-16 1971-09-16 Photographic elements containing ballasted resorcinols

Country Status (5)

Country Link
US (1) US3770431A (enrdf_load_stackoverflow)
BE (1) BE788926A (enrdf_load_stackoverflow)
CA (1) CA983765A (enrdf_load_stackoverflow)
FR (1) FR2153013B1 (enrdf_load_stackoverflow)
GB (1) GB1404470A (enrdf_load_stackoverflow)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4126461A (en) * 1977-06-13 1978-11-21 Eastman Kodak Company Black-and-white photographic elements and processes
US4175968A (en) * 1977-07-21 1979-11-27 Agfa-Gevaert, A.G. Color photographic materials containing anti-fogging agents
US4284714A (en) * 1979-05-09 1981-08-18 Fuji Photo Film Co., Ltd. Method of forming a photographic image
DE3226163A1 (de) * 1981-07-13 1983-01-20 Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa Farbphotographisches, lichtempfindliches silberhalogenidmaterial
US4411987A (en) * 1981-11-06 1983-10-25 Fuji Photo Film Co., Ltd. Silver halide color photographic light-sensitive material
US4439518A (en) * 1981-06-19 1984-03-27 Ciba-Geigy A.G. Process for the production of a photographic image
US4464463A (en) * 1982-07-26 1984-08-07 Fuji Photo Film Co., Ltd. Silver halide color photographic light-sensitive material
US5821039A (en) * 1997-05-30 1998-10-13 Eastman Kodak Company Photographic element containing neutral dye-forming resorcinol coupler
US5856072A (en) * 1997-06-02 1999-01-05 Eastman Kodak Company Photographic element containing 5-carbamoyl resorcinol interlayer scavenger
US5939247A (en) * 1997-10-29 1999-08-17 Oriental Photo Industrial Co., Ltd. Silver halide photographic material and a process for forming images
US6255045B1 (en) 2000-03-13 2001-07-03 Eastman Kodak Company Color photographic element containing improved polymeric disulfonamidophenol for scavenging oxidized developer

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3312549A (en) * 1962-12-12 1967-04-04 Eastman Kodak Co Receiving sheet for photographic dyes
US3362819A (en) * 1962-11-01 1968-01-09 Polaroid Corp Color diffusion transfer photographic products and processes utilizing an image receiving element containing a polymeric acid layer
US3582333A (en) * 1968-04-08 1971-06-01 Eastman Kodak Co Method for reducing color fog in color emulsions coated on electron bombarded supports

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3362819A (en) * 1962-11-01 1968-01-09 Polaroid Corp Color diffusion transfer photographic products and processes utilizing an image receiving element containing a polymeric acid layer
US3312549A (en) * 1962-12-12 1967-04-04 Eastman Kodak Co Receiving sheet for photographic dyes
US3582333A (en) * 1968-04-08 1971-06-01 Eastman Kodak Co Method for reducing color fog in color emulsions coated on electron bombarded supports

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4126461A (en) * 1977-06-13 1978-11-21 Eastman Kodak Company Black-and-white photographic elements and processes
US4175968A (en) * 1977-07-21 1979-11-27 Agfa-Gevaert, A.G. Color photographic materials containing anti-fogging agents
US4284714A (en) * 1979-05-09 1981-08-18 Fuji Photo Film Co., Ltd. Method of forming a photographic image
US4439518A (en) * 1981-06-19 1984-03-27 Ciba-Geigy A.G. Process for the production of a photographic image
DE3226163A1 (de) * 1981-07-13 1983-01-20 Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa Farbphotographisches, lichtempfindliches silberhalogenidmaterial
US4435503A (en) 1981-07-13 1984-03-06 Fuji Photo Film Co., Ltd. Silver halide color photographic light-sensitive material
US4411987A (en) * 1981-11-06 1983-10-25 Fuji Photo Film Co., Ltd. Silver halide color photographic light-sensitive material
US4464463A (en) * 1982-07-26 1984-08-07 Fuji Photo Film Co., Ltd. Silver halide color photographic light-sensitive material
US5821039A (en) * 1997-05-30 1998-10-13 Eastman Kodak Company Photographic element containing neutral dye-forming resorcinol coupler
US5856072A (en) * 1997-06-02 1999-01-05 Eastman Kodak Company Photographic element containing 5-carbamoyl resorcinol interlayer scavenger
US5939247A (en) * 1997-10-29 1999-08-17 Oriental Photo Industrial Co., Ltd. Silver halide photographic material and a process for forming images
US6255045B1 (en) 2000-03-13 2001-07-03 Eastman Kodak Company Color photographic element containing improved polymeric disulfonamidophenol for scavenging oxidized developer

Also Published As

Publication number Publication date
FR2153013B1 (enrdf_load_stackoverflow) 1977-04-01
DE2245445A1 (de) 1973-03-29
GB1404470A (en) 1975-08-28
CA983765A (en) 1976-02-17
BE788926A (fr) 1973-03-15
DE2245445B2 (de) 1976-12-02
FR2153013A1 (enrdf_load_stackoverflow) 1973-04-27

Similar Documents

Publication Publication Date Title
US3342599A (en) Schiff base developing agent precursors
US2756142A (en) Photographic color reproduction process
US3770431A (en) Photographic elements containing ballasted resorcinols
JPS60122940A (ja) 写真要素
US3180731A (en) Photothermographic elements and method of using same
US3635719A (en) Heat developable light-sensitive elements
US3772014A (en) Polymers containing resorcinol groups and photographic elements containing same
US3625685A (en) Photographic color diffusion-transfer element comprising aqueous film-forming synthetic polymer suspension layers intermediate its sensitive layers and processes for their use
US3377166A (en) Photographic image transfer process utilizing imidazole
US3856521A (en) Diffusion transfer color film and process
US3721562A (en) Integral laminate photographic units comprising developing composition-spreader sheets containing a polymeric acidifying layer
US3445228A (en) Dye diffusion transfer process and element
US3245789A (en) Photographic products and processes
JPS6332375B2 (enrdf_load_stackoverflow)
US4036643A (en) Diffusion transfer color process using lactone or sultone ring containing lipophilic non-diffusing color formers which yield diffusing dyes
US3753764A (en) Photographic diffusion transfer product and process
US3253915A (en) Photographic dye developer image transfer systems
US3592645A (en) Color prints of improved brightness
JPS5952422B2 (ja) カラ−写真画像の形成方法
US3418117A (en) Multicolor dye developer image transfer systems
US3642482A (en) Photographic element and process
US3201243A (en) Method of inhibiting discoloration of color photographic layers containing dye images and resulting photographic products
US4047952A (en) Imagewise soluble silver salt intensification of diffusion transfer silver images
US4503138A (en) Image-receiving element with unitary image-receiving and decolorizing layer
US3617272A (en) Multicolor dye developer systems