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
  • G03C7/407—Development processes or agents therefor
  • G03C7/413—Developers

Definitions

• This invention relates to a color developing solution for and a method of processing a light-sensitive silver halide color photographic material, and, more particularly, it relates to a color developing solution for and a method of processing a light-sensitive silver halide color photographic material being excellent in the photographic performances for fog and maximum density.
• the dye images are usually formed, after imagewise exposure, by reacting an oxidized p-phenylenediamine type color developing agent with a dye image-forming coupler.
• a color reproduction method according to the subtractive color process is usually used to form dye images of cyan, magenta and yellow respectively corresponding to red, green and blue.
• hydroxylamines and sulfites as preservative of the color developing solution.
• hydroxylamines are effective as the preservative for p-phenylenediamine type color developing solution.
• ammonia NH 3 acts with light-sensitive silver halide photographic material and causes ammonia fog on the light-sensitive material.
• hydroxylamines become to be further decomposable by the presence of heavy metal ions (e.g., Fe 3+ , Cu 2+ , etc.) contained in the color developing solution.
• heavy metal ions e.g., Fe 3+ , Cu 2+ , etc.
• chelating agents have been inspored and prodiced in order to chelate the heavy metal ions and inhibit their acts.
• these chelating agents there may be exemplified aminopolycarbonic acid, polyphosphoric acid, organic phosphoric acid, etc.
• these chelating agents are effective for Fe 3+ , they are less effective for Cu2+.
• the light-sensitive silver halide color photographic materials wherein a light-sensitive silver halide emulsion is substantially comprised of silver chloride can be rapidly developed as compared with conventional light-sensitive color photographic materials comprising a silver halide emulsion containing silver bromides or silver iodides such as silver chlorobromide, silver chloroiodobromide and silver iodobromide, and moreover can be free from accumulation in the color developing solution, of bromide ions or iodide ions which are susceptible to suppress development reactions.
• light-sensitive silver chloride color photographic materials wherein a light-sensitive silver chloride color photographic materials wherein a light-sensitive silver chloride emulsion is substantially comprised of silver chloride
• conventional light-sensitive color photographic materials comprising a silver halide emulsion containing silver bromides or silver iodides such as silver chlorobromide, silver chloroiodobromide and silver iodobromide, and moreover can
• the above-mentioned hydroxylamine conventionally used as one of preservatives tends to act as a developing agent for the silver chloride so that the silver development may proceed, to lower color density of color images finally obtained.
• the above-mentioned sulfite conventionally used as other preservatives tends to act as a dissolving agent for the silver chloride so that the physical development due to a color developing agent may rapidly proceed, to lose the balance between the silver development reaction and the coupling reaction; in other words, the silver development may overly precede and the coupling reaction may delay, whereby the color density is lowered.
• This fog may largely appear as a whole, and particularly largely has appeared in cyan color used for the purpose of preventing the decrease in color density.
• This heavy metal ion may raise a problem especially when a large quantity of light-sensitive materials is continuously processed.
• an object of this invention is to provide a color developing solution which can inhibit ammonia fog and effect chelating of heavy metal ions and does not cause excess development even when light-sensitive silver chloride color photographic material is employed, and a method employing the color developing solution.
• a color developing solution comprising the compound represented by General Formula (I) shown below and at least one compound selected from the compounds represented by General Formulas (II) and (III) shown below: wherein R 1 and R 2 each represent an alkyl group having 1 to 3 carbon atoms, wherein, in Formulas (II) and (III), R 1 , R 2 , R 3 , R4 , R9 and R 10 each represent a hydrogen atom, a halogen atom, a sulfonic acid group, an alkyl group having 1 to 7 carbon atoms, -OR 5 , -COOR 6 , or a phenyl group, wherein R 5 , R 6 , R 7 and R 8 each represent a hydrogen atom or an alkyl group having 1 to 18 carbon atoms, or by a method of processing a light-sensitive silver halide color photographic material having at least one silver halide emulsion layer, which comprises, after imagewise exposure of a light-
• the compound represented by General Formula (I) (hereinafter called the preservative of this invention) is used in place of hydroxylamine conventionally used as a preservative.
• R 1 and R2 each represent an alkyl group having 1 to 3 carbon atoms, and the alkyl group having 1 to 3 carbon atoms represented by R 1 and R 2 may be the same or different, including, for example, a methyl group, an ethyl group a n-propyl group, an iso-propyl group, etc.
• R 1 and R 2 are preferably both an ethyl group.
• These compounds of this invention are usually used in the form of salts such as hydrochloride, sulfate, p-toluenesulfonate, oxalate, phosphate and acetate.
• Concentration of the compound (I) of this invention in the color developing solution may be approximately the same as the concentration of the hydroxylamine usually used as a preservative, and it may be used preferably in concentration of 0.1 g/lit. to 50 g/lit., more preferably 0.5 g/lit. to 30 g/lit.
• N,N-diethylhydroxylamine for example, is known to be used as a preservative of a black and white developing agent in a color developing solution to which a black and white developing agent is added.
• the black and white developing agent i.e., hydroquinone, hydroquinonemonosulfonic acid, phenidone, p-aminophenol, etc. is relatively stable when used as the black and white developing agent in the black and white developing solution, and can be sufficiently preserved by using sulfite as a preservative, but, once it is added to a color developing solution, there takes place a cross oxidation reaction with a color developing agent, resulting in its very poor storage stability. Hydroxylamine is hardly effective for the preservation of the black and white developing agent added to such a color developing solution.
• N,N-diethylhydroxylamine is used as a preservative of the black and white developing agent added to a color developing solution
• phenidone in the so-called external color process, which is a process by which a light-sensitive color photographic material is developed according to a reversal process by using a color developing solution containing a coupler.
• a role of the phenidone is to increase the developing speed of the light-sensitive material of external system having poor developing performance and to increase the density of a dye image.
• a magenta color developing solution containing such phenidone, N,N-diethylhydroxylamine is also known to adversely affect the preservativity of the color developing solution of external system as it destroys the coupler (see Japanese Patent Publication No. 22198/1970).
• the compound of this invention has been conventionally known to be used as a preservative of the black and white developing agent added to a color developing solution, but has not been known as a preservative of a color developing agent in an ordinary color developing solution.
• the compound of this invention has been already known as a preservative of the black and white developing agent added to a color developing solution.
• the compound (I) can effectively act as a preservative of an ordinary color developing solution, but also the color density may not be lowered even when used in combination with a particular coupler shown below, and, by using the compound in combination with a chelating agent or agents represented by General Formula (II) and/or General Formula (III), generation of fog due to the contamination with heavy metals can be desirably prevented, and further, there can be obtained a developing solution having excellent stability without fall of pH and formation of tar.
• One of the conditions for the color developing solution used in this invention is to contain the sulfite in concentration of 2 x 10- 2 mole or less, preferably 4 x 10- 3 or less, per 1 liter of the color developing solution.
• the sulfite used in this invention may include sodium sulfite, potassium sulfite, sodium bisulfite, potassium bisulfite, etc.
• the color developing agent used in this invention contains at least one compound selected from the compound represented by General Formula (II) and the compound represented by General Formula (III) (hereinafter referred to as the chelating agent of this invention).
• R 1 , R 2 , R 3' R 4 , R 9 and R 10 each represent a hydrogen atom, a halogen atom, a sulfonic acid group, an alkyl group having 1 to 7 carbon atoms, -OR 5 , -COOR 6 , or a phenyl group
• R 5 , R 6 , R 7 and R 8 each represent a hydrogen atom or an alkyl group having 1 to 18 carbon atoms.
• the alkyl group represented by R 1 , R 2 , R 3 , R 4 , R 9 and R 10 may be substituted or unsubstituted and may include, for example, a methyl group, an ethyl group, an iso-propyl group, an n-propyl group, a t-butyl group, a n-butyl group, a hydroxymethyl group, a hydroxyethyl group, a methylcarboxylic acid group, a benzyl group, etc.
• the alkyl group represented by R 5 , R 6 , R 7 and R 8 may also include those same as the above, and may additionally include an octyl group.
• the phenyl group represented by R 1 , R 2 , R 3 , R4, R 9 and R 10 may include a phenyl group, a 2-hydroxyphenyl group, a 4-aminophenyl group, etc.
• Typical examples of the chelating agent of this invention are shown below, but by no means limited to these.
• 1,2-dihydroxybenzene-3,5- disulfonic acid which may be also used as alkali salts such as a sodium salt and a potassium salt.
• the above chelating agent represented by General Formula (II) or (III) of this invention may be used in the range of 5 mg to 20 g, preferably added in an amount of 10 mg to 10 g, more preferably 20 mg to 3 g, per 1 liter of the developing solution, to obtain good results.
• the chelating agent of this invention may be used alone or may be used in combination. There may be further used, in combination, other chelating agents such as aminopolyphosphonic acids such as aminotri(methylenephosphonic acid) and ethylenediaminetetraphosphoric acid, oxycarboxylic acids such as citric acid and gluconic acid, phosphonocarboxylic acids such as 2-phosphonobutane-l,2,4-tricarboxylic acid, polyphosphoric acids such as tripolyphosphoric acid and hexametaphosphoric acid.
• aminopolyphosphonic acids such as aminotri(methylenephosphonic acid) and ethylenediaminetetraphosphoric acid
• oxycarboxylic acids such as citric acid and gluconic acid
• phosphonocarboxylic acids such as 2-phosphonobutane-l,2,4-tricarboxylic acid
• polyphosphoric acids such as tripolyphosphoric acid and hexametaphosphoric acid.
• the color developing agent used in the color developing solution of this invention may preferably include p-phenylenediamine type compounds having a water soluble group.
• the p-phenylenediamine type compounds having a water soluble group have advantages not only that they may produce no stain on light-sensitive materials and hardly cause a rash on skin even if the skin was smeared with them, as compared with p-phenylenediamine type compounds having no water soluble group such as N,N-diethyl-p-phenylenediamine or the like, but also that they can afford to effectively achieve the objects of this invention by using them particularly in combination with the compound represented by General Formula ( I ) in this invention.
• the above water soluble group may be such that at least one water soluble group is possessed on an amino group or benzene ring of the p-phenylenediamine type compounds.
• Specific water soluble group may preferably include -(CH 2 ) n -CH 2 OH, -(CH 2 ) m NHS0 2 -( CH 2 )n- CH 3 , -(CH 2 ) m O-(CH 2 ) n -CH 3 , -(CH 2 CH 2 O) n C m H 2m+1 (m and n each represent an integer of 0 or more), a -COOH group, a -S0 3 H group.
• color developing agents those which can be preferably used in this invention as being free from generation of fog are compounds shown as exemplary Nos. (A-1), (A-2), (A-3), (A-4), (A-6), (A-7) and (A-15), and particularly preferable compound is No. (A-l).
• the above color developing agents are generally used in the form of salts such as hydrochloride, sulfate, p-toluenesulfonate, etc.
• the color developing agent having a water soluble group used in this invention, may be used preferably in the range of 1 x 10- 2 to 2 x 10 -1 mole per 1 liter of the color developing solution, more preferably from a viewpoint of the rapid processing, in the range of 1.5 x 10- 2 to 2 x 10- 1 mole per 1 liter of the color developing solution.
• the color developing solution of this invention may contain the following developing solution components, in addition to the above component.
• sodium hydroxide, potassium hydroxide, silicate, sodium metaborate, potassium metaborate, trisodium phosphate, tripotassium phosphate, borax, etc. may be used alone or in combination so far as the above effects of this invention, namely, the effect of no occurrence of precipitation and the effect of making the pH stable can be maintained.
• salts such as disodium hydrogenphosphate, dipotassium hydrogenphosphate, sodium bicarbonate, potassium bicarbonate and borate.
• organic amines such as ethanolamine, ethylenediamine, diethanolamine, triethanolamine, etc. It may also include benzyl alcohol disclosed in U.S. Patent No. 2,304,925, phenethyl alcohol, and besides these, acetylene glycol, methyl ethyl ketone, cyclohexane, thioethers, pyridine, ammonia, hydrazine, amines, etc.
• the bad soluble organic solvent particularly typified by benzyl alcohol tends to cause appearance of tar after use of the color developing solution for a long period of time, particularly during the running processing according to a low replenishing system. Appearance of such tar, when adhered on a paper light-sensitive material to be processed, may even bring about such a serious trouble that a commercial value of the product is extremely damaged.
• the bad solvent organic solvent does further have problems such that it has a great value for the burden to environmental pollution such as biochemical oxygen demand (BOD), and cannot be abandoned in sewerages, rivers or the like, so that much labor and cost are needed for waste liquor disposal. Accordingly, it is preferably used in a decreased amount, or not used.
• BOD biochemical oxygen demand
• An auxiliary developing agent can be also used together with the developing agent.
• Such an auxiliary developing agent is known to include, for example, N-methyl-p-aminophenol hexasulfate (Metol), phenidone, N,N'-diethyl-p-aminophenol hydrochloride, N,N,N'N'- tetramethyl-p-phenylenediamine hydrochloride, and may be added usually in an amount of 0.01 g to 1.0 g/lit.
• additives such as anti-stain agents, sludge preventive agents and interlayer effect accelerators can be used.
• the respective components of the above color developing agent can be prepared by successively adding them to a given amount of water, followed by stirring.
• a component having poor solvency to water may be added by mixing it with the above organic solvent such as triethanolamine.
• a mixture of a plurality of components that can be stably present together with each other prepared in the form of a concentrated aqueous solution or a solid in a small container, may be added in water and stirred to obtain a solution as the color developing solution of this invention.
• the above color developing agent can be used in a desired pH range, but, from a viewpoint of rapid processing, preferably in the range of pH 9.5 to 13.0, more preferably pH 9.8 to 13.0.
• the color developing processing temperature may be not lower than 30°C and not higher than 50 0 C, within which the higher it is, the more preferably it becomes possible to carry out rapid processing in a short time, but, from a viewpoint of image preservation stability, the temperature should not be so high.
• the processing is preferably carried out at not lower than 33°C and not higher than 45 0 C.
• the color developing is conventionally carried out in about 3 minutes and 30 seconds, but, in the present invention, it can be carried out in 2 minutes or less, or can be also carried out in the range of 30 seconds to 1 minute and 30 seconds.
• This invention can be applied in any system if it is a system using the color developing solution containing the compound represented by the above General Formula (I) and at least one compound selected from the compound represented by the above General Formula (II) and the compound represented by the above General Formula (III).
• a monobath processing system as well as other various types of processing systems such as a spray system in which a processing solution is formed into a spray, a web system utilizing the contact with a carrier impregnated with a processing solution, or a developing system using a viscous processing solution.
• the processing step should substantially comprise the steps of color developing, bleach-fixing and washing or stabilizing that can be substituted with the washing.
• the bleach-fixing step may be constituted separately of a bleaching step and a fixing step, or may comprise a bleach-fixing bath carrying out the bleaching and fixing in a bath.
• Bleaching agents that can be used in the bleach-fixing solution used in this invention are metal complex salts of organic acids.
• the complex salts are compounds formed by coordination of a metal ion such as iron, cobalt, copper, etc. with an organic acid such as aminopolycarboxylic acid or oxalic acid and citric acid.
• organic acid used for the formation of metal complex salts may include polycarboxylic acid.
• These polycarboxylic acid and aminopolycarboxylic acid may be alkali metal salts, ammonium salts or water soluble amine salts. Specific examples of these may include the following:
• bleaching agent may be used preferably in an amount of 5 to 450 g/lit., more preferably 20 to 250 g/lit.
• the bleach-fixing solution may contain a silver halide fixing agent in addition to the bleaching agent mentioned above, and, if necessary, a solution of the composition containing sulfite as a preservative may be used.
• the above halide that can be used may include, besides ammonium bromide, hydrochloric acid, hydrobromic acid, lithium bromide, sodium bromide, potassium bromide, sodium iodide, potassium iodide, ammonium iodide, etc.
• the bleach-fixing solution may contain, solely or in combination, a variety of pH buffering agents such as boric acid, borax, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, acetic acid, sodium acetate and ammonium hydroxide. It may also contain various brightening agents, anti-foaming agents or surface active agents.
• pH buffering agents such as boric acid, borax, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, acetic acid, sodium acetate and ammonium hydroxide. It may also contain various brightening agents, anti-foaming agents or surface active agents.
• preservatives such as bisulfite addition products of hydroxylamine, hydrazine or an aldehyde compound, organic chelating agents such as aminopolycarboxylic acid or stabilizers such as nitroalcohol and nitrate, and organic solvents such as methanol, dimethylsulfonamide and dimethylsulfoxide.
• various bleach accelerating-agents may be added, disclosed in Japanese Unexamined Patent Publication No. 280/1971, Japanese Patent Publications No. 8506/1970, and No. 556/1971, Belgian Patent No. 770,910, Japanese Patent Publications No. 8836/1970 and No. 9854/1978, Japanese Unexamined Patent Publications No. 71634/1979 and No. 42349/1974, etc. can be added.
• the bleach-fixing solution may be used at the p H of 4.0 or more, but, in general, at the pH of not less than 5.0 and not more than 9.5, more preferably at the pH of not less than 6.0 and not more than 8.5, and still more preferably at the pH of not less than 6.5 and not more than 8.5 to carry out the processing.
• the processing temperature to be used may be a temperature of not less than 3 0 C, preferably not less than 5°C, lower than the processing temperature in a color developing tank, and, desirably, a temperature of not less than 55° C while suppressing the evaporation or the like.
• washing or a process by use of washing solution substitute so-called washing substitutive stabilizing processing, in place of the washing.
• the process of the water washing substitute according to this invention is a process carried out in place of a water washing step following on a fixing step or a bleach-fixing step.
• Conventional water washing process is a process for washing away, by washing with water, a processing solution of a previous bath contained in structural layers of the light-sensitive material, specifically a large amount of thiosulfates, chemicals and silver complex salts contained in a fixing solution or a bleach-fixing soluiton, chemicals contained in a color developing solution and the like.
• This process includes, for example, a method in which a large amount of flowing water is flown on the surface of a light-sensitive material in a water washing bath to remove the processing solution of the provious bath, a substituting water washing method in which a light-sensitive material is dipped in a constant amount of water and the water is changed by fresh water after constant time passed, etc.
• this water washing process is usually carried out only by use of water, it may be conducted after dipping the light-sensitive material in a bath containing salts such as sodium sulfite, etc. for several minutes in order to accelerate the processing speed. In any event, the water processing is carried out by using water.
• the processing solution used for the process is not merely water, but a solution containing an antimildew, antiseptic, disinfection means, further optionally, a chelating agent having the chelating stabilization degree against ferric ion of 8 or more, ammonia compounds, organic acid salts, pH adjusting agents, surfactants, sulfites, brightening agents, etc.
• the compounds adhered or permeated in the light-sensitive material such as thiosulfates, etc. were washed away by replenishing water in about 5 lit. to 150 lit. per 1 m 2 of the light-sensitive material.
• the process of washing solution substitute of this invention such compounds adhered or permeated in the light-sensitive material is washed away by a replenished amount of about 0.01 lit. to 2.5 lit. per 1 m 2 of the light-sensitive material.
• washing solution substitute applicable in this invention The processing by use of washing solution substitute applicable in this invention will be described below.
• the pH of the washing soluiton substitute may range between 5.5 and 10.0.
• the p H -adjusting agents that can be contained in the washing solution substitute applicable in this invention may be any of those of alkali agents or acid agents generally known in the art.
• the processing by use of the washing solution substitute may be carried out at a temperature ranging between 15°C and 60° C , preferably 20°C and 45°C.
• the processing time as short as possible is also more preferable from a viewpoint of the rapid processing, but, in general, may be in the range of 20 seconds to 10 minutes, most preferably 1 minute to 3 minutes.
• washing solution substitute (or the stabilizing step) applicable in this invention may be supplied, in the case of a multiple tank counter current system, in such a manner that the solution is supplied to a posterior tank and overflowed from an anterior tank.
• the processing may be carried out in a single tank.
• various methods are available, including a method in which the compounds are added to a stabilizing tank in the form of a concentrated solution, or a method in which the above compounds and other additives are added to the washing soluiton substitute supplied to a stabilizing tank, and the resulting solution is used as a supplying solution for replenishing the washing solution substitute. Any of these method may be used for the addition.
• the processing by the washing soluiton substitute also refers to the processing for stabilizing, wherein stabilizing processing is carried out immediately after processing by a processing solution having bleach-fixing ability without substantially carrying out washing with water, and the processing solution used in such stabilizing solution is called the washing solution substitute, and the processing tank is called a washing solution substitute tank (or a stabilizing bath or a stabilizing tank).
• the stabilizing tank in the stabilizing processing applicable in this invention may preferably comprise 1 to 5 tanks, particularly preferably 1 to 3 tanks, and not more than 9 tanks at most.
• the method of processing the light-sensitive silver halide color photographic material of this invention is to process a light-sensitive silver halide color photographic material having a silver halide emulsion layer containing silver halide grains substantially comprised of silver chloride, by using the aforesaid color developing solution used in this invention, i.e., the color developing solution containing as preservatives the compounds of this invention, the compound (I).
• the silver halide grains used in the light-sensitive silver halide color photographic material applied in this invention are preferably substantially comprised of silver chloride.
• the terms "silver halide grains substantially comprised of silver chloride” are meant to be silver halide grains containing at least not less than 80 mole %, preferably not less than 90 mole %, and more preferably not less than 95 mole %, of silver chloride.
• the silver halide emulsion containing the above silver halide grains substantially comprised of silver chloride may contain, besides silver chloride, silver bromide and/or silver iodide as the silver halide composition.
• silver bromide may be contained in an amount of 20 mole % or less, preferably 10 mole % or less, more preferably 5 mole % or less.
• silver iodide may be contained in an amount of 1 mole % or less, preferably 0.5 mole % or less.
• Crystals of the silver halide grains used in this invention may be of regular crystals, twin crystals or others, and there can be used those having any ratio of [ 100] face to [ 111] face.
• the crystal structure of these silver halide grains may be uniform through inside to outside, or may be of layered structure comprising an inside and outside of different nature (a core/shell type).
• These silver halide grains may be also of the type such that a latent image is chiefly formed on the surface, or of the type wherein it is formed in the inside of a grain.
• Tabular silver halide grains see Japanese Unexamined Patent Publication No. 113934/1983 and Japanese Patent Application No. 170070/1984) can be also used.
• the silver halide grains used in this invention may be obtained by any preparation methods including an acidic method, a neutral method and an ammoniacal method.
• the silver halide grains according to this invention are preferably prepared in the above-mentioned manner.
• a composition containing such silver halide grains are referred to as a silver halide emulsion.
• the silver halide emulsion may be chemically sensitized by using active gelatin; sulfur sensitizing agents, for example, sulfur sensitizing agents such as allylthiocarbamide, thiourea and cystine; selenium sensitizing agents; reduction sensitizing agents, for example, stunnous salts, thiourea dioxide, polyamine, etc.; noble metal sensitizing agents, for example, gold sensitizing agents, specifically including sensitizing agents such as potassium aurothiocyanate, potassium chloroaurate and 2-aurothio-3-methylbenzothiazolium chloride, or sensitizing agents having a water soluble group, for example, ruthenium, palladium, platinum, rhodium, iridium, etc., specifically including ammonium chloropalladate, potassium chloroplatinate and sodium chloropalladate (Some of their act as a sensitizing agent or a fog-suppressing agent depends on whether they are in a large amount or a small amount.), etc
• the silver halide emulsion according to this invention may be subjected to chemical ripening by adding a sulfur-containing compound, and, before such chemical ripening, during the ripening, or after the ripening, at least one of hydroxytetrazaindenes and at least one of nitrogen-containing heterocyclic compounds having a mercapto group may be contained.
• the silver halide used in this invention may be optically sensitized by adding a suitable sensitizing dye in amount of 5 x 10- 8 mole to 3 x 10- 3 mole per mole of silver halide so that sensitivities to respectively desired light-sensitive wavelength regions can be imparted thereto.
• a suitable sensitizing dye in amount of 5 x 10- 8 mole to 3 x 10- 3 mole per mole of silver halide so that sensitivities to respectively desired light-sensitive wavelength regions can be imparted thereto.
• sensitizing dyes which sensitizing dyes can be used alone or in combination with two or more of them.
• the sensitizing dyes advantageously used in this invention may include, for example, the following:
• sensitizing dyes may be used alone or in combination of these.
• the light-sensitive photographic material of this invention may be optically sensitized to a desired wavelength region according to a spectral sensitization method by using a cyanine dye or a merocyanine dye alone or in combination.
• a particularly preferable spectral sensitization method may typically include the methods disclosed in Japanese Patent Publications No. 4936/1968, No. 22884/1968, No. 18433/1970, No. 37443/1972, No. 28293/1973, No. 6209/1974 and 12375/1978, Japanese Unexamined Patent Publications No. 23931/1977, No. 51932/1977, No. 80118/1979, No. 153926/1983, No. 116646/1984 and No. 116647/1984, etc., which are concerned with the combination of benzimidazolocarbocyanine with benzoxazolocarbocyanine.
• Those concerned with the combination of carbocyanine having a benzimidazole nucleus with other cyanines or merocyanines may include, for example, those disclosed in Japanese Patent Publications No. 25831/1970, No. 11114/1972, No. 25379/1972, No. 38406/1973 No. 38407/1973, No. 34535/1979 and No, 1569/1980, Japanese Unexamined Patent Publications No. 33220/1975, No. 38526/1975, No. 107127/1976, No. 115820/1976, No. 135528/1976, No. 104916/1977 and No. 104917/1977, etc.
• the methods concerned with the combination of thiacarbocyanine with other carbocyanines may include, for example, those disclosed in Japanese Patent Publications No. 4932/1968, No. 4933/1968, No. 26470/1970, No. 18107/1971 and N0. 8741/1972, Japanese Unexamined Patent Publication No. 114533/1984, etc., and the methods disclosed in Japanese Patent Publication No. 6207/1974, employing zeromethine- or dimethine- merocyanine, monomethine- or trimethinecyanine and styryl dyes, can be advantageously used.
• sensitizing dyes In adding these sensitizing dyes to the silver halide emulsion according to this invention, they are used as a dye solution obtained by previously dissolving them in a hydrophilic organic solvent such as methyl alcohol, ethyl alcohol, acetone, dimethylformamide and fluorinated alcohol disclosed in Japanese Patent Publication No. 40659/1975.
• a hydrophilic organic solvent such as methyl alcohol, ethyl alcohol, acetone, dimethylformamide and fluorinated alcohol disclosed in Japanese Patent Publication No. 40659/1975.
• They may be added at any time at the initiation of chemical ripening of the silver halide emulsions, during the ripening, or after completion of the ripening, or in some cases, at the step right before the coating of the emulsion.
• AI dyes Dyes that are water soluble or decolored by a color developing solution (AI dyes) may be added to photographic constituent layers of the light-sensitive silver halide color photographic material of this invention.
• the AI dyes may include oxonol dyes, hemioxonol dyes, merocyanine dyes and azo dyes. Among them, particularly useful are oxonol dyes, hemioxonol dyes and merocyanine dyes.
• examples of the AI dyes may include those disclosed in British Patents No. 584,609 and No. 1,277,429, Japanese Unexamined Patent Publications No. 85130/1973, No. 99620/1974, No. 114420/1974, No. 129537/1974, No.
• these AI dyes may be used preferably in an amount of 2 x 10- 3 to 5 x 10- 1 mole, more preferably 1 x 10- 2 to 1 x 10- 1 mole, per mole of silver in an emulsion layer.
• the processing method of the light-sensitive silver halide color photographic material of this invention is carried out by processing the light-sensitive silver halide material containing at least one selected from cyan couplers of (C - I), ( C -II) and (C - III) in at least one silver halide emulsion layer, by use of the color developing solution of this invention containing the compound of formula (I) as a preservative and the compound of formula (II) or (III) as a chelating agent.
• Y represents -CONHCOR 4 or -CONHS0 2 R 4 (where R 4 represents an alkyl group, an alkenyl group, a cycloalkyl group, an aryl group or a heterocyclic group; R 5 represents a hydrogen atom, an alkyl group, an alkenyl group, a cycloalkyl group, an aryl group or a heterocyclic group; and R 4 and R 5 may be bonded with each other to form a 5- or 6-membered ring); R3 represents a ballast group; and Z represents a hydrogen atom or a group eliminatable through the coupling reaction with the oxidized product of an aromatic primary amine series color developing agent.
• Y is a group represented by -COR 4 , -CONHCOR 4 or -CONHS0 2 R 4 .
• R4 represents an alkyl group, preferably an alkyl group having 1 to 20 carbon atoms (e.g. a methyl group, an ethyl group, a t-butyl group, a dodecyl group, etc.), an alkenyl group, preferably an alkenyl group having 2 to 20 carbon atoms (e.g.
• R 5 represents a hydrogen atom or a group represented by R 4 .
• R 4 and R 5 may be bound to each other to form a 5- or 6-membered heterocyclic ring containing a nitrogen atom.
• R 4 and R 5 may optionally have a substituent or substituents including, for example, an alkyl group having 1 to 10 carbon atom (e.g. ethyl, i-propyl, i-buytl, t-butyl, t-oxtyl, etc.), an aryl group (e.g.
• phenyl, naphthyl, etc. a halogen atom (fluorine, chlorine, bromine, etc.), a cyano group, a nitro group, a sulfonamido group (e.g. methansulfonamido, butansulfon- amido, p-toluenesulfonamido, etc.), a sulfamoyl group (e.g. methylsulfamoyl, phenylsulfamoyl, etc.), a sulfonyl group (e.g.
• a carbamoyl group e.g. dimethylcarbamoyl, phenylcarbamoyl, etc.
• an oxycarbonyl group e.g. ethoxycarbonyl, phenoxycarbonyl, etc.
• R 3 represents a ballast group necessary for providing a diffusion resistance to the cyan coupler represented by formulae (C - I) and (C - II)) and a cyan dye derived from said cyan coupler.
• R 3 may be an alkyl group having 4 to 30 carbon atoms, an aryl group or a heterocyclic group.
• R 3 may include a straight or branched alkyl group (e.g.
• Z represents a hydrogen atom or a group eliminatable through the coupling reaction with an oxidized product of color developing agent.
• z may include a halogen atom (e.g. chlorine, bromine, fluorine, etc.), a substituted or unsubstituted alkoxy, aryloxy, h eterocyclyloxy, acyloxy, carbamoyloxy, sulfonyloxy, al kylthio, arylthio, heterocyclicthio or sulfonamido group, etc. and more specifically, those as disclosed in U.S. Patent No. 3,741,563, Japanese Unexamined Patent Publication No.
• the cyan couplers represented by the above formulae (C - I) or (C - II) are more preferred.
• R34 is a substituted or unsubstituted aryl group (particularly preferred is a phenyl group).
• substituent for said aryl group represented by R 34 they may be mentioned at least one substituent selected from -SO 2 R 37 , a halogen atom (e.g. fluorine, bromine, chlorine, etc.), -CF 3 , -N 02 , -CN, -COR 37 , -COOR 37 , -SO 2 OR 37 , -OCOR 37 ,
• R16 represents an alkyl group, preferably an alkyl group having 1 to 20 carbon atoms (e.g. methyl, ethyl, tert-butyl, dodecyl, etc.), an alkenyl group, preferably an alkenyl group having 2 to 20 carbon atoms (e.g. an allyl group, a heptadecenyl group, etc.), a cycloalkyl group, preferably 5 to 7-membered ring group (e.g. a cyclohexyl group, etc.), an aryl group (e.g. a phenyl group, a tolyl group, a naphthyl group, etc.); and R 38 is a hydrogen atom or a group represented by the above R 37 .
• R 38 is a hydrogen atom or a group represented by the above R 37 .
• the preferred compounds of the phenol type cyan coupler represented by (C - IV) includes a compound in which R 37 is a substituted or unsubstituted phenyl group, and the substituent for the phenyl group includes a cyano group, a nitro group, -SO 2 R 39 (in which R 39 is an alkyl group), a halogen atom or a trifluoromethyl group.
• R 35 and R 36 each represent an alkyl group, preferably an alkyl group having 1 to 20 carbon atoms (e.g. methyl, ethyl, tert-butyl, dodecyl, etc.), an alkenyl group, preferably an alkenyl group having 2 to 20 carbon atoms (e.g. allyl, oleyl, etc.), a cycloalkyl group, preferably a 5- to 7-membered cyclic group (e.g. cyclohexyl, etc.), an aryl group (e.g.
• a phenyl group a tolyl group, a naphthyl group, etc.
• a heterocyclic group preferably a hetero ring of 5-membered or 6-membered hetero ring having 1 to 4 atoms of a nitrogen atom, an oxygen atom or a sulfur atom, such as a furyl group, a thienyl group, a benzothiazolyl group, etc.
• substituents may be introduced therein, and such substituents may be those which may be introduced in R 4 or R5 in formulae (C - I) and (C - II) as mentioned above.
• a halogen atom a chlorine atom, a fluorine atom, etc. is particularly preferred.
• ballast group represented by R 3 is a group represented by the following formula (C - VII):
• J represents an oxygen atom, a sulfur atom or a sulfonyl group
• k represents an integer of 0 to 4
• 1 represents 0 or 1; provided that when k is 2 or more, 2 or more of R41 may be the same or different from each other
• R40 represents a straight or branched alkylene group having 1 to 20 carbon atoms which may be substituted by an aryl group, etc.
• R 41 represents a monovalent group, preferably a hydrogen atom, a halogen atom (e.g. chlorine, bromine, etc.), an alkyl group, preferably a straight or branched alkyl group having 1 to 20 carbon atoms (e.g.
• an aryl group e.g. a phenyl group
• a heterocyclic group preferably a nitrogen containing heterocyclic group
• an alkoxy group preferably a straight or branched alkoxy group having 1 to 20 carbon atoms (e.g. methoxy, ethoxy, t-butyloxy, octyloxy, decyloxy, dodecyloxy, etc.)
• an aryloxy group e.g.
• an acyloxy group preferably an alkylcarbonyloxy group, an arylcarbonyloxy group (e.g. an acetoxy group, a benzoyl- oxy group), a carboxy group, an alkyloxycarbonyl group, preferably a straight or branched alkyloxycarbonyl group having 1 to 20 carbon atoms, an aryloxycarbonyl group, preferably a phenoxycarbonyl group, an alkylthio group preferably having 1 to 20 carbon atoms, an acyl group, a straight or branched alkylcarbonyl group which may preferably have 1-to 20 carbon atoms, an acylamino group, a straight or branched alkylcarboamide group which may preferably have 1 to 20 carbon atoms, a benzenecarboamido group, a sulfonamido group, preferably a straight or branched alkylsul
• cyan couplers of Formula (C-I) or (C-II) can be synthesized by the known method, and for example, they can be synthesized by the methods as disclosed in U.S. Patent Nos. 2,772,162, 3,758,308, 3,880,661, 4,124,396, 3,222,176, British Patent No. 975,773, 8,011,693 and 8,011,694; Japanese Unexamined Patent Publication Nos. Nos. 21139/1972, 112038/1975, 163537/1980, 29235/1981, 99341/1980, 116030/1981, 69329/1977, 55945/1981, 80045/1981 and 134644/1975; British Patent No. 1,011,940; U.S. Patent Nos.
• the cyan couplers represented by Formulae (C-I) and (C - III) in accordance with the present invention is typically used in an amount of about 0.005 to 2 moles, preferably 0.01 to 1 mole per one mole of silver.
• one of R and R1 represents a hydrogen atom and the other is a straight or branched alkyl group having 2 to 12 carbon atoms;
• X represents a hydrogen atom or a group eliminatable through the coupling reaction with an oxidized product of N-hydroxyalkyl substituted-p-phenylenediamine derivative color developing agent; and
• R2 represents a ballast group.
• the straight or branched alkyl group having 2 to 12 carbon atoms represented by R 1 and R of the above formula (C - III) are, for example, an ethyl group, a propyl group, a butyl group.
• the ballast group represented by R 2 is an organic group having a size and form which affords a coupler molecule bulkiness sufficient to substantially prevent the coupler from diffusing from the layer in which it has been contained to the other layers.
• the representative ballast group there may be mentioned an alkyl group or an aryl group each having total carbon atoms of 8 to 32, preferably those having total carbon atoms of 13 to 28.
• substituent for the alkyl group and the aryl group there may be mentioned, for example, an alkyl group, an aryl group, an alkoxy group, an aryloxy group, a carboxy group, an acyl group, an ester group, a hydroxy group, a cyano group, a nitro group, a carbamoyl group, a carbonamide group, an alkylthio group, an arylthio group, a sulfonyl group, a sulfonamide group, a sulfamoyl group, a halogen atom and the like, and as the substituent for the alkyl group, those as mentioned for the above aryl group except for the alkyl group.
• ballast groups are represented by the following formula:
• R 3 represents an alkyl group having 1 to 12 carbon atoms
• a r represents an aryl group such as a phenyl group, etc. and the aryl group may have a substituent.
• the substituent an alkyl group, a hydroxy group, a halogen atom, an alkylsulfonamido group, etc. may be mentioned and the most preferred is a branched alkyl group such as a t-butyl group, etc.
• the representative examples for x includes halogen represented by chlorine and fluorine, an aryloxy group, a substituted or unsubstituted alkoxy group, an acyloxy group, a sulfonamido group, an arylthio group, a heteroylthio group, a heteroyloxy group, a sulfonyloxy group, a carbamoyloxy group and the like.
• x there may be mentioned the groups as disclosed in Japanese Unexamined Patent Publication Nos.
• the cyan coupler of formula (C - III) of this invention may be preferably added in an amount of 2 x 10- 3 to 5 x 10- 1 mole, more preferably 1 x 10- 2 to 3 x 10- 1 mole per 1 mole of silver contained in the red-sensitive silver halide emulsion layer, but the amount of cyan coupler of formula (C - III) is not limitative.
• the above couplers (C - I) to (C - III) of this invention may be used with other cyan couplers in combination.
• cyan couplers which may be used in combination there may be included phenol type compounds, naphtol type compounds, etc. and may be selected from those described in US Patent Nos. 2,369,929, 2,434,272, 2,474,293, 2,895,826, 3,253,924, 3,034,892, 3,311,476, 3,386,301, 3,418,390, 3,458,315, 3,591,383, etc.
• the cyan couplers represented by the formulae (C - I) to (C - I I I) may-be used in combination with the conventionally known cyan couplers so long as it does not contradict to the object of the present invention. Further, the cyan couplers represented by formulae (C - I) to (C - III) may be used in combination therewith.
• Magenta couplers for photography may include compounds of pyrazolone type, pyrazolotriazole type, pyrazolinobenzimidazole type, and indazolone type.
• the pyrazolone type magenta couplers may include the compounds disclosed in U.S. Patents No. 2,600,788, No. 3,062,653, No. 3,127,269, No. 3,311,476, No. 3,419,391, No. 3,519,429, No. 3,558,318, No. 3,684,514 and No. 3,888,680, Japanese Unexamined Patent Publications No. 29639/1974, No. 111631/1974, No. 129538/1974 and No. 13041/1975, Japanese Patent Publications No.
• the pyrazolotriazole type magenta couplers may include the couplers disclosed in U.S. Patent No. 1,247,493 and Belgian Patent No. 792,525.
• nondiffusion colored magenta couplers there may be generally used the compounds arylazo-substituted at the coupling position of a colorless magenta coupler, which may include, for example, the compounds disclosed in U.S. Patents No. 2,801,171, No. 2,983,608, No. 3,005,712 and No. 3,684,514, British Patent No. 937,621, Japanese Unexamined Patent Publications No. 123625/1974 and No. 31448/1974.
• the colored magenta couplers of the type such that a dye may flow out into a processing solution by the reaction with an oxidized product of a developing agent can be also used.
• yellow couplers for photography conventionally used are open-chain ketomethylene compounds, and there can be used benzoylacetanilide type yellow couplers and pivaroylacetanilide type couplers widely used in general.
• Two equivalent type yellow couplers wherein a carbon atom at the coupling position is substituted with a substituent eliminable through the coupling reaction can be also used. Examples of these, together with synthesis methods thereof, are disclosed in U.S. Patents No. 2,875,057, No. 3,265,506, No. 3,664,841, No. 3,408,194, No. 3,277,155, No. 3,447,928 and No. 3,415,652, Japanese Patent Publication No. 13576/1974, Japanese Unexamined Patent Publications No. 29432/1973, No. 68834/1973, No. 10736/1974, No. 122335/1974, No. 28834/1975 and No. 132926/1975, etc.
• the above nondiffusion couplers in this invention may be used generally in an amount of 0.05 mole to 2.0 moles per mole of silver in the light-sensitive silver halide emulsion.
• a DIR compound may be preferably used.
• a compound capable of releasing a development restrainer along with development may be also included in this invention, which may include, for example, the compounds disclosed in U.S. Patents No. 3,297,445 and No. 3,379,529, West German Patent Publication (OLS) No. 24 17 914, Japanese Unexamined Patent Publications No. 15271/1977, No. 9116/1978, No. 123838/1984 and No. 127038/1984, etc.
• the DIR compound used in this invention is a compound capable of releasing a development restrainer through the reaction with an oxidized product of a color developing agent.
• Such a DIR compound may typically include DIR couplers wherein a group capable of forming a compound having a development restraining action has been introduced to a coupler active site when eliminated from the active site, which are disclosed, for example, in British Patent No. 935,454, U.S. Patents No. 3,227,554, No. 4,095,984 and No. 4,149,886, etc.
• the above DIR couplers have a property that a coupler mother nucleus may form a dye and, on the other hand, a developing restrainer is released when coupled with an oxidized product of a color developing agent.
• a developing restrainer is released when coupled with an oxidized product of a color developing agent.
• a compound capable of releasing a development restrainer but not forming any dye when coupled with an oxidized product of a color developing agent as disclosed in U.S. Patents No. 3,652,345, No. 3,928,041, No. 3,958,993, No. 3,961,959 and No. 4,052,213, Japanese Unexamined Patent Publications No. 110529/1978, No. 13333/1979 and No. 161237/1980, etc.
• timing DIR compound which is a compound such that a mother nucleus may form a dye or colorless' compound when reacted with an oxidized product of a color developing agent, and on the other hand, an eliminated timing group may release a development restrainer through the intramolecular nucleophilic substitutive reaction or elimination reaction.
• timing DIR compound wherein the timing group as mentioned above has been attached onto a coupler mother nucleus capable of forming a perfectly diffusing dye when reacted with an oxidized product of a color developing agent, as disclosed in Japanese Unexamined Patent Publications No 160954/1983 and No. 162949/1983.
• the DIR compound contained in the light-sensitive material may be used preferably in an amount ranging between 1 x 10 -4 mole to 10 x 10 -1 mole per mole of silver.
• the light-sensitive silver halide color photographic material used in this invention may additionally contain a variety of additives for photography.
• additives for photography there may be used antifoggants, stabilizers, ultraviolet absorbent, color stain preventive agents, brightening agents, color image-fading preventive agents, antistatic agents, hardening agents, surface active agents, plasticizers, wetting agents, etc. which are disclosed in Research Disclosure No. 17643.
• hydrophilic colloid used for preparing an emulsion may include any of proteins such as gelatin, derived gelatin, graft polymers of gelatin with other macromolecules, albumin and casein; cellulose derivatives such as hydroxyethyl cellulose derivatives and carboxymethyl cellulose; starch derivatives; synthetic hydrophilic macromolecules of homopolymers or copolymers such as polyvinyl alcohol, polyvinyl imidazole and polyacrylamide; etc.
• Supports for the light-sensitive silver halide color photographic material used in this invention may include, for example, baryta paper, polyethylene-coated paper, polypropylene synthetic paper, transparent supports provided with a reflection layer in combination, or using a reflecting body in combination, for example, glass plates, polyester films of cellulose acetate, cellulose nitrate or polyethylene terephthalate, polyamide films, polycarbonate films, polystyrene films, etc., and may also include other conventional transparent supports. These supports may be selected depending on what the light-sensitive materials are used for.
• various coating methods can be used, including dip coating, air doctor coating, curtain coating, hopper coating, etc.
• a coating method of simultaneously applying two or more layers can be also used, according to the method disclosed in U.S. Patents No. 2,761,791 and No. 2,941,898.
• the respective emulsion layers may be applied in any positional order arbitrarily determined.
• a blue-sensitive silver halide emulsion layer in the case of light-sensitive materials for full color photographic paper, it is preferred to arrange a blue-sensitive silver halide emulsion layer, a green-sensitive silver halide emulsion layer and a red-sensitive silver halide emulsion layer in this order from the support side.
• These light-sensitive silver halide emulsion layers may each comprise two or more layers.
• an intermediate layer or layers with appropriate thickness may be optionally provided depending on the purpose, and various layers such as a filter layer, an anticurl layer, a protective layer and an antihalation layer can be also used in appropriate combination as constituent layers.
• various layers such as a filter layer, an anticurl layer, a protective layer and an antihalation layer can be also used in appropriate combination as constituent layers.
• the above hydrophilic colloid that can be used in emulsion layers can be similarly used as a binding material therefor, and also in the layers the above-mentioned various additives that can be contained in emulsion layers can be contained.
• the method of processing a light-sensitive silver halide color photographic material of this invention can be applied to any light-sensitive silver halide color photographic materials such as color paper, color negative films, color positive films, color reversal films for slides, color reversal films for motion pictures, color reversal films for televisions, and reversal color paper, if the light-sensitive silver halide color photographic material is a light-sensitive material to be processed according to the so-called internal development system wherein couplers are contained in the light-sensitive material substantially containing the above silver,chloride.
• the processing method of this invention has made it possible to provide a color developing soluiton for processing a light-sensitive silver halide color photographic material that can achieve excellent storage stability and excellent photographic performances for fog and maximum density, and is particularly feasible for rapid processing, and a method employing the same.
• the following layers were provided by coating on paper supports laminated with polyethylene, successively in the order from the support side to produce samples of light-sensitive materials.
• Silver halide compositions of respective silver halide emulsion are shown below in Table 2.
• Processing solutions used had the following composition.
• Samples No. 3 to No. 10 having 80 % or more of silver chloride content show that the developing completion time is short and they are feasible for rapid processing.
• Samples No. 5 to No. 10 having 90 % or more of silver chloride content especially, Samples No. 6 to 10 having 95 % or more of silver chloride content are particularly feasible for the rapid processing.
• Example 2 was repeated by using the same color developing solution as in Example 1 and the light-sensitive material as used in Example 2 (Sample No. 8) in accordance with the same procedural steps in Example 2, provided for using the color developing solution as used in Example 1 was left to stand for one week by an open top ratio of 10 cm 2 /lit. and setting the color development time to 45 seconds.
• Example 2 Using color paper samples used in Example 2, similar processing was repeated following the processing steps in Example 2 and using the processing solutions used in Example 2.
• the silver halide composition in the color paper samples was made to be 1 : 99 of AgBr : AgCl in the blue-sensitive emulsion layer, 5 : 95 in the green-sensitive emulsion layer, and 5 : 95 in the red-sensitive emulsion layer.
• Cyan couplers used were as shown in Table 4. Color developing processing time was 45 seconds. Concentration of potassium sulfite in the color developing solution was controlled as shown in Table 4. Chelating agents as shown in Table 4 were used in amount of 1.0 g/lit.
• the color developing solution used was obtained by adding 4 ppm of a ferric ion, 2 ppm of a copper ion and 1000 ppm of a calcium ion (added by dissolving FeCl 3 , CuS0 4 -6H 2 0 and CaCl2, respectively), and stored for 5 days under the same conditions in Example 1.
• the maximum color density and minimum color density of the cyan dye after processing were measured to obtain the results shown in Table 4.
• Example 5 Using the light-sensitive color photographic materials produced in Example 2 (silver halide composition is shown in Table 5), the following processing was carried out to evaluate silver-developing properties on the color developing solutions Nos. 2, 4 and 6 (containing no color developing agent). Standard processing steps: (Processing temperature and processing time)
• spectral reflection density was measured on the samples by orange light to evaluate D max of the samples. Difference between the spectral reflection density for D max and the spectral reflection density for D min was assumed as a typical characteristic of silver density.
• the decrease in density is particularly remarkable when 1.0 x 10- 2 or more of potassium sulfite is present, but, in the cases where the couplers of this invention are used, it is seen that the cyan density decreases only a little, and further that very good maximum density can be obtained when the concentration of sulfite is 4.0 x 10- 3 or less.
• the following layers were provided by coating on paper supports laminated with polyethylene, successively in the order from the support side to produce samples of light-sensitive materials.
• the silver halide composition in each of the silver halide emulsions is shown in Table 7.
• Processing solutions used had the following composition.
• Samples No. 80 to No. 87 having 80 % or more of silver chloride content show that the developing completion time is short and they are feasible for rapid processing.
• Samples No. 82 to No. 87 having 90 % or more of silver chloride content especially, Samples No. 83 to 87 having 95 % or more of silver chloride content are particularly feasible for the rapid processing.
• Example 7 Using color paper samples used in Example 7, similar processing was repeated following the processing steps in Example 7 and using the processing solutions used in Example 7. However, the silver halide composition in the color paper samples was made to be 3 : 97 of AgBr : AgCl in the blue-sensitive emulsion layer, 3 : 97 in the green-sensitive emulsion layer, and 1 : 99 in the red-sensitive emulsion layer. Cyan couplers used were as shown in Table 8. Color developing processing time was 45 seconds. Concentration of potassium sulfite in the color developing solution was controlled as shown in Table 8.
• Chelating agents as shown in Table 8 were used in amount of 1.0 g/lit:
• the color developing solution used was obtained by adding 4 ppm of a ferric ion, 2 ppm of a copper ion and 100 ppm of a calcium ion (added by dissolving FeCl 3 , CuS04 ⁇ 6H20 and CaCl2, respectively), and stored for 5 days under the same conditions in Example 1.
• the maximum color density and minimum color density of the cyan dye after processing were measured to obtain the results shown in Table 8.
• Example 9 Using the light-sensitive color photographic materials produced in Example 7 (silver halide composition is shown in Table 9), the following processing was carried out to evaluate silver-developing properties on the color developing solutions Nos. 2, 4 and 6. Standard processing steps: (Processing temperature and processing time)
• Example 7 Using Samples 78, 80 and 83 used in Example 7 (provided that cyan couplers used are shown in Table 10), and also using the developing solution No. 6 used in Example 1 as a color developing solution (provided that potassium sulfite used is as shown in Table 10), the influence to the cyan density (maximum reflection density) by the silver halide composition and sulfite was examined. Developing processing and evaluation method were in accordance with Example 7.
• the decrease in density is particularly remarkable when 1.0 x 10- 2 or more of potassium sulfite is present, but, in the cases where the couplers of this invention are used, it is seen that the cyan density decreases only a little, and further that very good maximum density can be obtained when the concentration of sulfite is 4.0 x 10- 3 or less.

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