Classifications

• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
  • G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
  • G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
  • G03C7/3046—Processing baths not provided for elsewhere, e.g. final or intermediate washings

Definitions

• This invention relates to silver halide photographic elements and, in particular, to compositions of a stabilizing solution which provide enhanced dye stability.
• the processing of silver halide photographic elements generally involves the steps of color evolution, bleaching, fixing, stabilizing and drying.
• the stabilizing bath is used as the final step in the processing of photographic elements in order to reduce stain and/or to enhance dye stability.
• the stability of the dye image is believed to be affected by the presence of unreacted coupler in the emulsion layers, because the coupler and the dye can react slowly with one another in a redox reaction to degrade the color image. In particular, the image from magenta dye tends to fade much more rapidly than either the cyan or the yellow dye image.
• Stabilizing solutions are aqueous formulations that contain a compound which reacts with the residual dye coupler in the emulsion layer to deactivate it and prevents its reaction with the dye and subsequent degradation of the color image.
• the present invention is particularly concerned with aldehydic dye stabilizing agents.
• Formaldehyde is a preferred aldehydic dye stabilizing agent because of its high volatility. Any residual formaldehyde on the photographic element is readily removed in a drying step.
• concerns over the hazardous effects of formaldehyde have led to increased efforts in developing alternative dye stabilizing agents or in reducing the amount of formaldehyde used in the stabilizing solution without compromise to the stabilizing solution performance.
• a novel stabilizing solution is used to provide dye stability to photographic elements.
• the stabilizing solution advantageously prevents dye fade by deactivating the dye coupler remaining in the processed photographic elements.
• An aqueous stabilizing solution comprises an aldehydic dye stabilizing agent and a secondary amine in an amount sufficient to activate the aldehydic dye stabilizing agent.
• the use of a secondary amine in the stabilizing solution is based on the discovery that it activates the reaction between the aldehydic stabilizing agent and the dye coupler.
• the rate of coupler deactivation is increased, thereby permitting use of reduced levels of dye stabilizing agent without compromise to the dye stabilizing properties of the solution or, alternatively, permitting use of aldehydic dye stabilizing agents containing higher aldehydes that were heretofore insufficiently active with respect to dye stabilization.
• second amine is used herein in the conventional sense that the amine contains two nitrogen-carbon bonds, that is, N(C-X)2H, where X is any substituent.
• higher aldehydes as that term is used herein, it is meant aldehydes possessing a substituent group containing at least one carbon atom.
• reduced levels as that term is used herein, it is meant that the amount of aldehydic dye stabilizing agent used in the stabilizing solution in the presence of a secondary amine is less than the amount that would be required to stabilize the dye in the absence of a secondary amine.
• insufficiently active it is meant that the coupler deactivation reaction either does not occur at a perceptible rate or proceeds too slowly under the processing conditions described herein to be of practical use.
• activity and activation are used herein with reference to the rate of dye coupler deactivation.
• the secondary amine has the formula: wherein each of R 1 and R 2 is an alkyl group, a substituted alkyl group, an aromatic group or a substituted aromatic group.
• the alkyl group may contain four or fewer carbon atoms.
• the substituted alkyl group may have solubilizing moieties, in which case there may be up to seven carbon atoms in the alkyl group.
• a most preferred amine is diethanolamine.
• the secondary amine is a cyclic amine having the formula: wherein the cyclic group contains four to six carbon atoms, X is an oxygen or nitrogen atom and a is 0 or 1. Most preferably, the cyclic amine is morpholine or piperidine.
• a solubilizing agent is added to the solution in an amount sufficient to solubilize the secondary amine.
• Preferred solubilizing agents include co-solvents such as ethylene glycol and diethylene glycol.
• the stabilizing solution of this invention can be used to provide improved dye stability with any of a wide variety of color photographic elements.
• the stabilizing solution can be advantageously employed in the processing of photographic elements designed for reversal color processing or in the processing of negative color elements or color print materials.
• the stabilizing solution can be employed with photographic elements which are processed in color developers containing couplers or with photographic elements which contain the coupler in the silver halide emulsion layers or in layers contiguous thereto.
• the photosensitive layers present in the photographic elements processed according to the method of this invention can contain any of the conventional silver halides as the photosensitive material, for example, silver chloride, silver bromide, silver bromoiodide, silver chlorobromoiodide, and mixtures thereof.
• These layers can contain conventional addenda and be coated on any of the photographic supports, such as, for example, cellulose nitrate film, cellulose acetate film, polyvinyl acetal film, polycarbonate film, polystyrene film, polyethylene terphthalate film, paper, polymer-coated paper, and the like.
• the photographic elements which are advantageously treated with the stabilizing solution of this invention are elements comprising a support having thereon at least one, and typically three or more, hydrophilic colloid layers containing a dye image. Any of a wide variety of colloids can be utilized in the production of such elements.
• colloids include naturally occurring substances such as proteins, protein derivatives, cellulose derivatives, for example, cellulose esters, gelatin, for example, alkali-treated gelatin (cattle bone or hide gelatin) or acid treated gelatin (pig-skin gelatin), gelatin derivatives - for example, acetylated gelatin, phthalated gelatin and the like, polysaccharides such as dextran, gum arabic, zein, casein, pectin, collagen derivatives, collodion, agar-agar, arrowroot albumin and the like.
• naturally occurring substances such as proteins, protein derivatives, cellulose derivatives, for example, cellulose esters, gelatin, for example, alkali-treated gelatin (cattle bone or hide gelatin) or acid treated gelatin (pig-skin gelatin), gelatin derivatives - for example, acetylated gelatin, phthalated gelatin and the like, polysaccharides such as dextran, gum arabic, zein, casein, pec
• the bleaching agent is typically a ferric complex of an aminopolycarboxylic acid, for example, the ferric complex of ethylenediaminetetraacetic acid (EDTA) or the ferric complex of 1,3-propylenediaminetetraacetic acid (PDTA) or a mixture of the ferric complex of EDTA and the ferric complex of PDTA.
• EDTA ethylenediaminetetraacetic acid
• PDTA 1,3-propylenediaminetetraacetic acid
• the fixing agent is typically a thiosulfate, such as sodium thiosulfate or ammonium thiosulfate, or a thiocyanate, such as ammonium thiocyanate, or a mixture of a thiosulfate and a thiocyanate.
• a thiosulfate such as sodium thiosulfate or ammonium thiosulfate
• a thiocyanate such as ammonium thiocyanate
• Processes employing the stabilizing solution of this invention can vary widely in regard to the particular processing steps utilized.
• the process can comprise only the two steps of color developing and bleach-fixing, followed by the stabilizing step, or it can comprise the three steps of color developing, bleaching, and fixing, followed by the stabilizing step.
• it can be a color reversal process in which the processing baths utilized are a first developer, a reversal bath, a color developer, a bleach, and a fix, followed by the stabilizing bath.
• the stabilizing solution of the present invention prevents dye fade by providing a dye stabilizing agent which deactivates the dye coupler remaining in the photographic element after treatment as described above.
• Use of a secondary amine in the stabilizing solution serves to enhance the activity of the aldehydic dye stabilizing agent.
• the secondary amine interacts with the aldehydic dye stabilizing agent to form a highly reactive, positively charged intermediate which, in turn, readily reacts with and thereby deactivates the dye coupler. It has been discovered that secondary amines are effective catalysts for reactions of the aldehydic dye stabilizing agent with the dye coupler.
• the reaction may involve the intermediate formation of a cationic Schiff base according to eq. 1. An uncharged Schiff base intermediate which is less reactive does not form when using a secondary amine.
• an increase in the rate of magenta dye coupler deactivation by the aldehydic dye stabilizing agent was observed in the presence of a secondary amine.
• a five-fold increase in the rate of magenta dye coupler deactivation was observed for formaldehyde.
• the increased rate of dye coupler deactivation permits a five-fold decrease in the formaldehyde level without degradation of the stabilizing solution properties.
• Reduced formaldehyde levels are highly desirable due to the growing concerns regarding the health hazards of formaldehyde.
• Typical prior art stabilizing solutions have formaldehyde levels ranging from 0.75 to 2.0 g/L.
• the stabilizing solution of the present invention possesses acceptable dye stabilizing performance with formaldehyde levels below 0.5 g/L and preferably in the range of 0.1-0.5 g/L.
• the secondary amine can be used at levels approximately at least one tenth the molar concentration of the dye stabilizing agent and typically in the range 0.05 to 0.20 the molar concentration of the dye stabilizing agent.
• aldehydes in general are not as reactive as formaldehyde in dye coupler deactivation reactions. For example, no acceptable level of activity is observed with acetaldehyde in the absence of a secondary amine unless the process is carried out with high excesses of the aldehyde.
• the addition of a secondary amine increases the activity of the aldehyde, which is defined as the rate of the dye coupler deactivation, so that the claimed aldehydes can be used under the processing conditions described hereinabove.
• the aldehyde is present at its solubility limit or preferably at a level of 5.0 g/L.
• the secondary amine is present at a level sufficient to activate the aldehyde. Typically, the amine is approximately one tenth the molar concentration of the aldehyde.
• the amine may be used at a concentration in the range of 0.05 to 1.00 g/L.
• the amine can be any secondary amine that is soluble in the stabilizing solution.
• Secondary amines that are preferred for use in the stabilizing baths of this invention have the formula: wherein each of R 1 and R 2 is an alkyl group, a substituted alkyl group, an aromatic group or a substituted aromatic group. Solubility of the amine in the stabilizing solution is obtained in several ways. If the alkyl group is nonpolar, it should contain four or fewer carbon atoms. However, if the substituted alkyl group contains solubilizing substituents, the amount of carbon atoms in the alkyl group can increase to seven. Solubilizing substituents can include, for example, hydroxy, sulfoxy and carboxyl groups. Diethanolamine is a preferred secondary amine.
• cyclic amines having the formula: wherein the cyclic group contains four to six carbon atoms, X is an oxygen or nitrogen atom and a is 0 or 1. Cyclic amines are particularly preferred because the reduced steric hindrance associated with cyclic compounds promotes the formation of the reactive intermediate. Preferred cyclic amines include morpholine and piperidine.
• aldehydic dye stabilizing agents can be used in the stabilizing solution of the invention.
• Secondary amines have been found to accelerate the reactions of most aldehydic dye stabilizing agents.
• Particularly useful agents include aliphatic aldehydes such as formaldehyde, paraformaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, glutaraldehyde and valeraldehyde and aromatic aldehydes such as benzaldehyde, furfural, vanillin and anisaldehyde.
• ingredients utilized in making up the stabilizing solution of this invention can be used in any suitable amount and the optimum amount of each will vary widely depending on a number of factors such as the particular compounds employed, the manner of treating the photographic element with the stabilizing solution and the particular type of photographic element to be treated.
• additives can also be incorporated into the stabilizing solution with beneficial results.
• useful additives include wetting agents, buffering agents and biocides. Wetting agents are particularly useful when processing color negative film to avoid water spotting. Organosiloxane wetting agents are especially beneficial.
• Biocides are useful to prevent microbial growth in both processes for color films and processes for color papers.
• a particularly useful class of biocides for this purpose are the thiazole compounds, especially isothiazolines such as 1,2-benzisothiazolin-3-one, 2-methyl-4-isothiazolin-3-one, 2-octyl-4-isothiazolin-3-one and 5-chloro-N-methyl-4-isothiazolin-3-one.
• the accelerated dye fade test was accomplished by an oven keeping method in which the film is incubated to 77 ° C at 40% relative humidity to accelerate the redox reaction responsible for dye fade. The film is then evaluated against a neutral dye patch. Dye intensities are determined and reported in Table 1 as densities corrected to a density of 1.0. Negative numbers indicate a loss of dye intensity. Performances were judged by comparison to stabilizing solutions to control solutions.

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• 1993
  • 1993-06-28 EP EP93110274A patent/EP0577041A2/fr not_active Withdrawn
  • 1993-06-29 JP JP15903693A patent/JPH0659423A/ja active Pending

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