US3549364A - Photographic processes and compositions - Google Patents

Photographic processes and compositions Download PDF

Info

Publication number
US3549364A
US3549364A US690728A US3549364DA US3549364A US 3549364 A US3549364 A US 3549364A US 690728 A US690728 A US 690728A US 3549364D A US3549364D A US 3549364DA US 3549364 A US3549364 A US 3549364A
Authority
US
United States
Prior art keywords
silver halide
silver
image
energy
developing agent
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
US690728A
Other languages
English (en)
Inventor
Meroe M Morse
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.)
Polaroid Corp
Original Assignee
Polaroid Corp
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 Polaroid Corp filed Critical Polaroid Corp
Application granted granted Critical
Publication of US3549364A publication Critical patent/US3549364A/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
    • G03C5/00Photographic processes or agents therefor; Regeneration of such processing agents
    • G03C5/26Processes using silver-salt-containing photosensitive materials or agents therefor
    • G03C5/29Development processes or agents therefor
    • G03C5/30Developers
    • 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
    • G03C8/02Photosensitive materials characterised by the image-forming section
    • G03C8/04Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of inorganic or organo-metallic compounds derived from photosensitive noble metals
    • G03C8/06Silver salt diffusion transfer

Definitions

  • Photographic processes for forming a silver image by diffusion transfer are well known.
  • Processes for forming a usable negative image along with the positive silver transfer image are also known.
  • a lightsensitive silver halide emulsion which has been exposed to contain a developable image is typically contacted with an aqueous alkaline processing composition including a silver halide solvent and a silver halide developing agent; exposed and developable silver halide is reduced to image silver to form a negative image and at substantially the same time an imagewise distribution of a soluble silver complexe is formed in terms of unexposed areas of the emulsion.
  • This imagewise distribution is transferred at least in part, by imbibition, to a superposed image-receiving layer where it is reduced to image silver to form a pOSitive silver transfer image.
  • the present invention is directed to developing compositions which obviate or greatly reduce the need for aftertreatment.
  • the present invention is directed to processing compositions for use in silver diffusion transfer processes for forming a usable negative image along with a positive silver transfer image, the compositions including the novel combination of a high energy aminophenol silver halide developing agent containing in one or both of the positions ortho to the phenolic hydroxyl group an amino, alkyl or alkoxy group; and a low energy ascorbic acid or hydroxylamine silver halide developing agent, the low energy developing agent being present in substantially greater concentration than the high energy developing agent, the amount of each of the developing agents alone being insufficient to develop appreciable negative density, but the respective amounts together providing a synergistic effect whereby the combination of developing agents in the processing compositions is capable of providing, upon development, a negative image having a desired usable density.
  • the processing composition further includes at least one silver halide solvent and at least one alkaline material in sufiicient quantity to provide a pH of at least 10.5.
  • the processing composition containing the aforementioned novel combination of silver halide developing agents further includes as the silver halide solvent or complexing ingredients the combination of cysteine and a nitrogenous base, as described and claimed in applicants US. Pat. No. 3,343,958.
  • the processing composition is further characterized by having a pH of from 10.5 to about 12.5.
  • the present invention is directed to novel processing compositions for use in diffusion transfer systems for preparing a usable negative silver image along with a positive silver transfer image and to photographic processes employing the same.
  • a primary object of this invention is to provide novel products and processes of the foregoing description.
  • Another object is to provide novel silver halide developing compositions which obviate or greatly reduce the need for after-treatment to obtain stable silver images.
  • the invention accordingly comprises the several steps and the relation and order of one or more of such steps with respect to each of the others, and the product possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure, and the scope of the application of which will be indicated in the claims.
  • high-energy silver halide developing agents are known.
  • One class of these known high-energy developers are the aminophenols, e.g., 4-amino-phenols having a lower alkyl, lower alkoxy, and/ or an amino group in a position or the positions ortho to the phenolic hydroxyl group.
  • Particularly useful examples of such high energy silver halide developing agents include 2,4-diamino-ortho-cresol, 4-amino-2,6-dimethyl-phenol and 2,6-dimethoxyl-4-aminophenol.
  • Such a high-energy silver halide developing agent may be employed in extremely low concentrations if it is employed in combination with a high concentration of a low-energy silver halide developing agent.
  • the synergistic effects so obtained greatly expands the usefulness of such high-energy silver halide developing agents.
  • Particularly useful low-energy silver halide developing agents are those which have substantially colorless oxidation products and/or are volatilized from the image, particularly the ascorbic acids, such as ascorbic acid, isoascorbic acid, etc., and hydroxylamines,
  • Suitable hydroxylamine silver halide developing agents include those disclosed in U.S. Patents Nos. 2,857,276, is sued to Edwin H. Land et al., and 3,287,125 issued to Milton Green, Adnan A. Sayigh and Henri Ulrich.
  • compositions containing the novel synergistic combination of developing agents of this invention have been found, according to the present invention, to be particularly useful in photographic systems wherein one desires to obtain a fully developed and fixed negative silver image of good density, contrast and stability along with a positive silver transfer image.
  • Processing compositions in which the combination of developing agents of this invention are intended to be employed in such processes in general further include a silver halide solvent or fixing agent, e.g., sodium or potassium thiosulfate, etc. and an alkaline material such as sodium hydroxide, diethylamine, sodium carbonate, etc. in an amount suflicient to provide a pH of at least 10.5, preferably from 10.5 to about 12.5 With a pH below about 10.5 the development time is appreciably slower.
  • a silver halide solvent or fixing agent e.g., sodium or potassium thiosulfate, etc.
  • an alkaline material such as sodium hydroxide, diethylamine, sodium carbonate, etc.
  • any of the known complexing ingredients may be contained in the processing compositions contemplated by this invention, of particular use is the combination of complexing ingredients disclosed in my U.S. Patent No. 3,343,958.
  • a nitrogenous base e.e., diethylamine
  • the processing compositions may also contain additional reagents performing specific desired functions, e.g., viscosity-increasing, film-forming materials such as sodium carboxymethyl cellulose, hydroxyethyl cellulose, etc.; antifoggants, preservatives, toning agents, etc.
  • the respective ingredients of the processing composition may be present initially in the aqueous medium therefor, or any or all of them may be present initially in the photographic product, e.g., the photosentitive element or the image-receiving element, in which case the desired composition may be formed by applying thereto the aqueous medium, e.g., during the development step.
  • EXAMPLE 1 A photosensitive element having a silver iodobromide emulsion on a film base was exposed and then developed by spreading between the thus exposed emulsion and a superposed surface hydrolyzed cellulose acetate sheet a processing composition comprising the following proportions of ingredients:
  • Aqueous solution of sodium sulfide (156mg. Na S/cc.)-
  • Aqueous solution of lead acetate and cadmium acetate (100 cc. H O, 2.9 g. lead acetate; 2.1 g. cadmium acetate)0.34 cc.
  • the spreader sheet was removed to reveal a fully developed and fixed negative on the photosensitive element and a good quality positive silver transfer image in the solidified layer of processing fluid adhered to the hydrolyzed surface of the cellulose acetate sheet.
  • EXAMPLE 2 A photosensive element having a silver iodobromide emulsion on film base was exposed and processed by spreading a layer of processing fluid, approximately 0.0020 thick, between the exposed negative and a surface hydrolyzed sheet of cellulose acetate.
  • the processing fluid comprised:
  • Aqueous solution of sodium sulfide of sodium sulfide (156 mg. Na S/cc.)0.0l1 cc.
  • the cellulose ace tate sheet was separated from the exposed negative to provide a negative silver image, and a positive silver transfer image in a solidified layer of processing fluid adhered to the hydrolyzed surface of the cellulose acetate sheet.
  • Aqueous solution of lead acetate and cadmium acetate (100 cc. H O, 2.9 g. lead acetate; 2.1 g. cadmium acetate)0.36 cc.
  • EXAMPLE 4 The procedures described in the preceding examples were repeated using baryta paper instead of the cellulose acetate sheet. The solidified layer of processing fluid adhered to the baryta paper when it was separated from the developed negative.
  • the silver precipitating nuclei for initiating and facilitating reduction of silver halide to image silver were present initially in the processing fluid.
  • Such procedures are described, forexample, in U.S. Patent No. 2,662,822 issued to Edwin H. Land.
  • the silver precipitating nuclei may alternatively be present in the silverreceptive stratum, e.g., to provide one of the vigorous silver precipitating environments described, for example, in U.S. Pats. Nos. 2,698,237 and 2,698,245 issued to Edwin H. Land.
  • EXAMPLE 5 A photosensitive element having a silver iodobromide emulsion on a film base was exposed and then developed by spreading between the thus-exposed emulsion and a superposed surface hydrolyzed cellulose acetate sheet a processing composition comprising the following proportions of ingredients:
  • Example 5 was repeated eliminating the ascorbic acid from the developing composition. An extremely faint (D 0.15 above base density) image was obtained.
  • Example 5 was repeated eliminating the 2,4diaminoorthocresol from the developing composition. The resulting image was even fainter or had an even lower density (D 0.05 above base density) than the negative prepared in Example 6.
  • the following example represents developing time series analyses illustrating the effect of pH upon development time.
  • EXAMPLE 8 A light-sensitive silver iodobromide emulsion was exposed and then developed with a first processing composition having a pH above 11.0 and comprising the following proportions of ingredients:
  • a second set of development times were run by exposing and developing a similar light-sensitive emulsion with a second processing composition in which the amounts of sodium hydroxide and diethylamine were adjusted so that the processing composition had a pH of 8.5 to 9.0.
  • composition 3 afforded lower D s and required longer development times than did composition 1.
  • EXAMPLE 10 The negative image prepared in Example 5 was subjected to accelerated tests for stability to light, heat and humidity (ultraviolet lamp for 72 hours; relative humidity at F. for 40 hours; 80% relative humidity at F. for 16 hours in the presence of powdered sulfur), and was found to be exceptionally stable although perhaps not of archival stability.
  • a fully developed and fixed negative prepared as described in Example 1 has been found to be stable, e.g., no density fading and density increase in highlights, when stored at room temperature and humidity for over two years.
  • a photographic process comprising the steps of contacting an exposed light-sensitive silver halide emulsion containing a developable image with an aqueous alkaline processing composition having a pH above 10.5 and including a silver halide solvent, a high energy aminophenol silver halide developing agent containing in a position ortho to the phenolic hydroxyl group at least one substituent selected from the group consisting of amino, lower alkyl and lower alkoxy groups and a low-energy silver halide developing agent selected from the group consisting of ascorbic acids and hydroxylamines, said low-energy developing agent being present in substantially greater concentration than said high-energy developing agent, the amount of each of said low-energy and high-energy developing agents alone being insuflicient to develop appreciable negative density, but said respective amounts together providing a synergistic effect whereby said combined developing agents are capable of developing exposed silver halide to a desired usable density;
  • a process as defined in claim 1 wherein said highenergy silver halide developing agent is 4-amino-2,6-dimethyl-phenol and said low-energy silver halide developing agent is isoascorbic acid.
  • a photographic processing composition for use in processes for forming silver transfer images comprising an aqueous alkaline solution containing a silver halide solvent, a high-energy aminophenol silver halide developing agent containing in a position ortho to the phenolic hydroxyl group at least one substituent selected from the group consisting of amino, lower alkyl and lower alkoxy groups and a low-energy silver halide developing agent selected from the group consisting of ascorbic acids and hydroxyl amines, said low-energy developing agent being present in substantially greater concentration than said high-energy developing agent, the amount of each of said low-energy and high-energy silver halide developing agent alone being insufiicient to develop appreciable negative density, but said respective amounts together providing a synergistic effect whereby said combined developing agents are capable of developing exposed silver halide to a desired usable density, said processing composition having a pH above 10.5.
  • composition as defined in claim 9 wherein the pH of said composition is between 10.5 and about 12.5.
  • composition as defined in claim 9 wherein said high-energy silver halide developing agent is 2,4-diaminoortho-cresol.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
US690728A 1965-03-08 1967-12-15 Photographic processes and compositions Expired - Lifetime US3549364A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US43804465A 1965-03-08 1965-03-08
US69072867A 1967-12-15 1967-12-15

Publications (1)

Publication Number Publication Date
US3549364A true US3549364A (en) 1970-12-22

Family

ID=27031523

Family Applications (1)

Application Number Title Priority Date Filing Date
US690728A Expired - Lifetime US3549364A (en) 1965-03-08 1967-12-15 Photographic processes and compositions

Country Status (2)

Country Link
US (1) US3549364A (fr)
NL (1) NL6602944A (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3723117A (en) * 1969-10-27 1973-03-27 Agfa Gevaert Method for developing silver halide emulsions
EP0476613A2 (fr) * 1990-09-19 1992-03-25 Dainippon Ink And Chemicals, Inc. Procédé pour former des images négatives à très haut contraste
US5399457A (en) * 1993-10-15 1995-03-21 Minnesota Mining And Manufacturing Company Process for reducing sludge in diffusion transfer printing plates
WO2004001504A1 (fr) * 2002-05-15 2003-12-31 Dianne Iverglynne Solution de developpement biodegradable et son procede d'utilisation
FR3076214A1 (fr) * 2017-12-28 2019-07-05 L'oreal Procede de coloration d'oxydation mettant en œuvre un substrat portant au moins un colorant d'oxydation, plusieurs conservateurs, et une composition aqueuse oxydante

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2060596A (en) * 1934-06-09 1936-11-10 Agfa Ansco Corp Photographic developer
US2857276A (en) * 1954-11-23 1958-10-21 Polaroid Corp Photographic processes and compositions useful therein
US3022168A (en) * 1958-06-28 1962-02-20 Pharmacia Ab Photographic developer
US3041170A (en) * 1959-10-29 1962-06-26 Eastman Kodak Co New class of development promoter precursors for dry processing self-developing silver halide coatings
US3134673A (en) * 1960-02-19 1964-05-26 Ilford Ltd Photographic developers

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2060596A (en) * 1934-06-09 1936-11-10 Agfa Ansco Corp Photographic developer
US2857276A (en) * 1954-11-23 1958-10-21 Polaroid Corp Photographic processes and compositions useful therein
US3022168A (en) * 1958-06-28 1962-02-20 Pharmacia Ab Photographic developer
US3041170A (en) * 1959-10-29 1962-06-26 Eastman Kodak Co New class of development promoter precursors for dry processing self-developing silver halide coatings
US3134673A (en) * 1960-02-19 1964-05-26 Ilford Ltd Photographic developers

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3723117A (en) * 1969-10-27 1973-03-27 Agfa Gevaert Method for developing silver halide emulsions
EP0476613A2 (fr) * 1990-09-19 1992-03-25 Dainippon Ink And Chemicals, Inc. Procédé pour former des images négatives à très haut contraste
EP0476613A3 (en) * 1990-09-19 1992-06-03 Dainippon Ink And Chemicals, Inc. Superhigh contrast negative image forming process
US5217842A (en) * 1990-09-19 1993-06-08 Dainippon Ink And Chemical, Inc. Superhigh contrast negative image forming process
US5399457A (en) * 1993-10-15 1995-03-21 Minnesota Mining And Manufacturing Company Process for reducing sludge in diffusion transfer printing plates
EP0649062A2 (fr) * 1993-10-15 1995-04-19 Minnesota Mining And Manufacturing Company Procédé pour réduire la formation de boue dans des plaques d'impression pour le procédé de diffusion-transfert
EP0649062A3 (fr) * 1993-10-15 1995-08-16 Minnesota Mining & Mfg Procédé pour réduire la formation de boue dans des plaques d'impression pour le procédé de diffusion-transfert.
WO2004001504A1 (fr) * 2002-05-15 2003-12-31 Dianne Iverglynne Solution de developpement biodegradable et son procede d'utilisation
FR3076214A1 (fr) * 2017-12-28 2019-07-05 L'oreal Procede de coloration d'oxydation mettant en œuvre un substrat portant au moins un colorant d'oxydation, plusieurs conservateurs, et une composition aqueuse oxydante

Also Published As

Publication number Publication date
NL6602944A (fr) 1966-09-09

Similar Documents

Publication Publication Date Title
US2592368A (en) Gelatine silver halide emulsion layer containing a dihydroxy diphenyl tanning developing agent
US2647056A (en) One step photographic transfer process
US2500421A (en) Photographic silver halide transfer process
US2635048A (en) Photographic transfer product and process
GB714412A (en) Improvements in or relating to photographic process and agent
US2725298A (en) Transfer process of photographic printing
GB454622A (en) Improvements in colour photography
US3549364A (en) Photographic processes and compositions
US3087816A (en) Photographic diffusion transfer process
US3769014A (en) Beta-disulfone silver halide solubilizing agents
US2449153A (en) Photographic silver bromide emulsion sensitized with cysteine
GB687751A (en) Process and material for the direct production of positive photographic images
US3189454A (en) Method of photographic development and fixing
US3721562A (en) Integral laminate photographic units comprising developing composition-spreader sheets containing a polymeric acidifying layer
US3740221A (en) Development of photographic material
US3265502A (en) Photographic developing compositions
US3265501A (en) Water-swellable colloidal magnesium aluminum silicate photographic composition
GB800772A (en) Improvements in processes of photographic reproduction
US3343958A (en) Monobath containing cysteine-nitrogenous base combination
US3515555A (en) Toning composition for direct positive paper
US3640713A (en) Photographic processes and compositions therefor
US2939788A (en) Novel photographic developers
US2984565A (en) Photographic process and composition
US3563740A (en) Use of dicyanamides in and with photosensitive systems
US3620728A (en) Receiving sheet for diffusion transfer processes