JP2630472B2 - Processing method of silver halide color photographic light-sensitive material - Google Patents

Description

Description: FIELD OF THE INVENTION The present invention relates to a method for processing a silver halide color photographic light-sensitive material, and more particularly to a continuous processing method for regenerating and using a color developing solution using an ion exchange membrane electrodialysis method. .

(Prior Art) In a processing method of a silver halide color photographic light-sensitive material, a used processing solution is generally discarded as an overflow solution.

However, these used processing liquids collected and treated as waste liquids have a large pollution load value, which is not preferable in terms of environmental conservation, and the collection and delivery costs for the recovery cannot be ignored.

In particular, regarding the color development process of color photographic photosensitive materials,
Conventionally, there are various methods for reducing waste liquid because of high alkali pollution and large organic pollutant load expressed in BOD (Biochemical Oxygen Demand) and very large waste liquid pollutant load and expensive chemicals. A method has been proposed.

For example, a low replenishment processing method in which the replenishment amount is reduced by adjusting the composition of a replenisher of a color developing solution (hereinafter, referred to as a color developing replenisher) has been carried out, as disclosed in JP-A-61-251852 and JP-A-61-251852. 2617
No. 41, No. 61-282841, and No. 61-70552. Adjustment of replenisher composition in low replenishment processing
Even if the amount of replenishment is reduced, the necessary amount of ingredients will be supplied,
For example, there is a measure for thickening consumable components such as a color developing agent and a preservative in a replenisher. Further, when a silver halide color photographic light-sensitive material is processed, halogen ions are released into the color developing solution.
In particular, the bromine ion concentration in the color developer increases, resulting in suppression of development. Therefore, in order to prevent this, measures such as reducing the bromide concentration in the replenisher in comparison with the normal replenishment treatment are generally performed. However, it also has certain limitations, and the progress of development is delayed due to the accumulation of bromine ions, and delicate fluctuations in bromine ion concentration change photographic properties. This tendency is mainly caused by silver iodobromide emulsions. This is more noticeable in the processing of photosensitive materials.

On the other hand, as a means for reducing the waste liquid, a method of reusing a used treatment liquid (overflow liquid) as a replenisher has been studied. If reuse becomes possible, the above-mentioned problems in waste liquid treatment will be solved, and the active ingredient remaining in the overflow solution can be reused. The amount of chemical used is reduced, and further cost reduction can be achieved. Therefore,
As a rejuvenation treatment, the fluctuations that occurred during processing were reworked, i.e., generally to remove accumulated components that adversely affect photographic performance and to be consumed so that the spent processing solution could be reused. There have been many studies on so-called regeneration techniques, in which a deficient component is added and used again as a replenisher.

In the reproduction technique, how to effectively remove the accumulated component is a conventional problem. In the color development process, it is particularly important to remove bromine ions which are eluted from the photosensitive material and exhibit a strong development suppressing action. It was an issue.

For example, halogen removal method using ion exchange resin is SM
PTE J., 88 , 168-171 (1979); JP-A-55-144240;
53-131243. However, this method requires large-scale equipment such as a resin column, requires techniques for controlling halogen ions, and can perform only batch-type treatment. Further, a large amount of waste liquid is generated for resin regeneration, so this waste liquid treatment requires a new method. Problems arise.

Further, a method for removing halogen by an ion exchange membrane electrodialysis method is described in JP-B-61-52459, JP-A-51-97432, and the like. The bromine ions in the solution are detected and quantified, and the amount of halogen ions in the developer, particularly bromine ions, is removed by dialysis so as to maintain a constant concentration by controlling the amount of electricity supplied to the electrodialysis tank based on the result. A continuous processing method in which the insufficient processing agent component is added to the overflow solution at this time and used again as a replenisher is disclosed in JP-A-54-37731 and JP-A-56-2.
No. 7142.

(Problems to be Solved by the Invention) According to the ion exchange membrane electrodialysis method, continuous operation is possible and the adjustment of halogen ions is also possible, so that the handling is easier and the equipment space is smaller than the ion exchange resin method. There is an advantage that it is necessary. However, in the case of controlling the halogen ion concentration to be kept constant in the continuous treatment using the ion exchange membrane electrodialysis method,
Fluctuations in current density, fluctuations in halogen detection accuracy, concentration of the developer, etc., cause subtle changes in the concentration of halogen ions, especially when processing silver halide color photographic materials.
There has been a problem that the obtained photographic performance (especially sensitivity and gradation) tends to fluctuate.

Accordingly, the present invention provides a method for processing a silver halide color photographic light-sensitive material capable of stably obtaining excellent photographic performance in a developing waste liquid regenerating system using an ion exchange membrane electrodialysis method. Aim.

(Means for Solving the Problems) The object of the present invention is to process a silver halide color photographic light-sensitive material while regenerating a color developing solution by an ion exchange membrane electrodialysis method using an anion exchange membrane and a cation exchange membrane. In the method, the silver halide color photographic light-sensitive material has at least one silver iodobromide emulsion layer having a silver bromide content of 80 mol% or more, and has a bromide ion equilibrium concentration of 6.0 × 10 5 in a developing solution.
^{-3 to} 1.3 × 10 ^-2 mol / at a constant concentration, and the replenishment amount of the color developing solution is ² per 1 m ^{2 of the} photosensitive material.
It has been found that the problem can be solved by a method for processing a silver halide color photographic light-sensitive material, wherein the amount is from 00 to 1500 ml.

In particular, when a light-sensitive material having a coated silver amount of 2 to 6 g / m ² is used, the eluted halogen ion concentration is in the most easily controllable region, and the photographic property fluctuation due to running is stabilized, and excellent running performance is obtained. be able to.

Moreover, even at relatively many replenishing amount of running the replenishing amount of about 200~1500ml / m ² of the color developing solution, the concentration of accumulated halogen is in the prone regions to control, photographic properties vary with the running is reduced .

In a developer regeneration system using an ion exchange membrane electrodialysis method, a color photographic light-sensitive material containing a silver iodobromide emulsion having a high silver bromide content is processed according to the present invention, and bromine in the developer is treated. Stable photographic performance by controlling the ion concentration to any one of 6.0 × 10 ^{−3 to} 1.3 × 10 ⁻² mol /, preferably 8 × 10 ^{−3 to} 1.2 × 10 ⁻² mol / Was obtained.

By controlling the bromine ion concentration in the developer in ion exchange membrane electrodialysis to a slightly higher concentration than in the past,
Surprisingly, it is possible to suppress a slight change in the concentration of the halogen ion in the developer, and it is possible that the composition in the developer becomes relatively high-activity and high-suppression type and that the silver iodobromide emulsion of the present invention is contained. It is presumed that the use of the color light-sensitive material made it less likely to be affected by the fluctuation of the bromine ion concentration.

In the present invention, the bromine ion concentration in the developer is 6.0 × 1
Controlling to a certain concentration of 0 ^{-3 to} 1.3 × 10 ^-3 mol / means that the certain concentration to be controlled is within any of the above-mentioned concentration ranges, Including that the density further fluctuates within a certain deflection range. The deflection width is ± 1 × 10 ⁻³ mol / in bromine ion concentration,
It is preferably in the range of 0.5 × 10 ⁻³ mol /.

The ion exchange membrane electrodialysis method to which the present invention is effectively applied is disclosed in JP-B-52-34939, JP-B-61-52459, and JP-A-51-84.
No. 636, No. 51-85722, No. 51-97432, No. 52-119934
No. 53-149331, No. 53-46732, No. 54-9626,
No. 54-19741, No. 53-7324, No. 52-146236, No. 52
Nos. 143018 and 54-58028, the bromine ion concentration in the developer to be regenerated was measured, and the bromine ion concentration in the developer was determined to be within the above range. Any method may be used as long as it is an electrodialysis method for a developing waste liquid having a device for adjusting the amount of electricity supplied so as to have a constant concentration.

Specifically, a desalting chamber of an ion exchange membrane electrodialysis tank comprising a plurality of anion exchange membranes and a plurality of cation exchange membranes between a cathode and an anode (a cation exchange membrane on the cathode side, and a A chamber separated by an anion exchange membrane) and the developer tank 1 of the processor are connected to each other, and the developer is circulated between the desalting chamber and the developer tank. The waste developer can be regenerated through a controlled amount of current so that the ion concentration is constant according to the present invention.

A plurality of deionization chambers are provided by alternately providing and partitioning a plurality of cation exchange membranes and a plurality of anion exchange membranes between a cathode and an anode provided inside the ion exchange membrane dialysis tank main body 11. A plurality of concentrating chambers are formed.

Further, a cathode chamber and an anode chamber are formed by being partitioned by an ion exchange membrane provided adjacent to the both electrode plates.

The developing solution is supplied to the desalting chamber from the supply line 12, is subjected to electrodialysis, is discharged from the outflow line 13, and is supplied to the developing solution tank 1.

Further, a sodium sulfate solution or the like is supplied from a supply line 14 to the concentration chamber, the anode chamber, and the cathode chamber, and is discharged from an outflow line 15 after electrodialysis.

Materials for the cathode of the ion exchange membrane dialysis tank include iron, nickel, stainless steel, and the like, and materials for the anode include graphite, magnetite, platinum, platinum-plated titanium, and the like. There is no particular limitation on the cation exchange membrane,
As the anion exchange membrane, an exchange membrane that selectively permeates monovalent anions, particularly bromine ions and iodine ions, is desirable.

An alkaline solution such as sodium hydroxide solution or potassium hydroxide solution, a salt solution such as sodium sulfate,
Or supply a solution of an acid such as sulfuric acid. The concentration of these solutions may be about 0.1 normal, there is no particular upper limit, and usually 1 normal or less is sufficient. A developer is supplied from a developer tank to a desalting chamber of the ion exchange membrane dialysis tank. The supply method may be such that the respective desalting chambers are connected in parallel, or the respective desalting chambers may be connected in series.

When the developer with reduced processing capacity and the fatigued solution is poured into the desalting chamber of the ion-exchange membrane dialysis tank and electrodialysis is performed, bromine ions and iodine ions in the developer pass through the anion exchange membrane and are concentrated or concentrated. Moved and removed to the anode compartment. Further, cations (for example, sodium ions) in the developer are moved to and removed from the concentration chamber or the cathode chamber through the cation exchange membrane. For this reason, in the desalination chamber, the concentration of bromine ions, iodine ions, cations, etc. decreases, and this solution is again
The developer is circulated by being supplied to the developer tank 1 by 13. In the concentration chamber, the concentration of these ions increases and is discharged through line 15.

Current density leading to an ion-exchange membrane electrodialysis, varies depending on the characteristics and properties of the development waste liquid of the ion exchange membrane is suitably ^{0.02A / dm 2 ~10A / dm 2} , more preferably 0.1 A / dm it is a ^{2 ~3A} / dm ^2. Further, it is also possible to supply the electrolyte solution (concentration chamber liquid) passing through the concentrating chamber with an amount of water corresponding to the amount of development processing and to circulate while maintaining the electrolyte concentration of the concentrating chamber liquid constant.

On the other hand, as shown in FIG. 1, the overflow solution of the developing solution is normally stored in a stock tank 21, and when a certain amount is stored, the overflow solution is transferred to a solution adjusting tank 22, and an insufficient component is added from a tank 24 as a regenerating agent. To the specified volume (amount of liquid preparation),
The obtained liquid can be transferred to the replenisher stock tank 23 and reused as a developing replenisher.

The regeneration method of the present invention includes at least two kinds of bromine ions, chloride ions, sulfate ions, thiocyan ions, sulfite ions, carbonate ions, phosphate ions, borate ions, nitrate ions, phosphonate ions, and bicarbonate ions. All of the above effects can be exerted on ordinary developers containing the above ions.

The color developing solution used in the present invention contains a known aromatic primary amine color developing agent. A preferred example is a p-phenylenediamine derivative, representative examples of which are shown below, but are not limited thereto.

D-1 N, N-diethyl-p-phenylenediamine D-2 2-amino-5-diethylaminotoluene D-3 2-amino-5- (N-ethyl-N-laurylamino) toluene D-4 4- [ N-ethyl-N- (β-hydroxyethyl) amino] aniline D-5 2-methyl-4- [N-ethyl-N- [β-hydroxyethyl) amino] aniline D-6 4-amino-3-methyl -N-ethyl-N-
[Β- (methanesulfonamido) ethyl] aniline D-7 N- (2-amino-5-diethylaminophenylethyl) methanesulfonamide D-8 N, N-dimethyl-p-phenylenediamine D-9 4- Amino-3-methyl-N-ethyl-N-methoxyethylaniline D-10 4-Amino-3-methyl-N-ethyl-N-β
-Ethoxyethylaniline D-11 4-amino-3-methyl-N-ethyl-N-β
-Butoxyethylaniline Among the above p-phenylenediamine derivatives, particularly preferred is compound D-5.

Further, these p-phenylenediamine derivatives may be salts such as sulfate, hydrochloride, sulfite, and p-triene sulfonate. The amount of the aromatic primary amine color developing agent used is preferably about 0.1 g / color developing solution.
A concentration of about 20 g, more preferably about 0.5 g to about 10 g.

Further, as a preservative, a sulfite such as sodium sulfite, potassium sulfite, sodium bisulfite, potassium bisulfite, sodium metasulfite, potassium metasulfite, or a carbonyl sulfite adduct is added to the color developing solution as needed. be able to.

The preferable amount of the preservative is 0.5 g per color developing solution.
To 10 g, more preferably 1 g to 5 g.

Further, the aromatic primary amine color developing agent directly,
As the preserving compounds, various hydroxylamines, hydroxamic acids described in Japanese Patent Application No. 61-186559,
Hydrazines and hydrazides described in No. 56, 61-1887
Phenols described in Nos. 42 and 61-203253, 61-18
It is preferable to add α-hydroxyketones and α-aminoketones described in 8741 and / or various saccharides described in 61-180616. Further, in combination with the above compounds, Japanese Patent Application Nos. 61-147823, 61-166664, 61-165621 and 61-165621.
Monoamines described in 61-164515, 61-170789 and 61-168159, 61-173595 and 61-164515
No. 61-186560 and diamines described in No. 61-1656
Nos. 21 and 61-169789, polyamines described in 61-169789,
Polyamines described in 188619, nitroxy radicals described in 61-197760, 61-186561, and 61-197419
It is preferable to use the alcohols described in No. 61-198987, the oximes described in No. 61-198987, and the tertiary amines described in No. 61-265149.

Other preservatives include JP-A Nos. 57-44148 and 57-5.
Various metals described in 3749, salicylic acids described in JP-A-59-180588, alkanolamines described in JP-A-54-3532, polyethyleneimines described in JP-A-56-94349, U.S. Pat. An aromatic polyhydroxy compound described in 3,746,544 may be contained as necessary. Particularly, addition of an aromatic polyhydroxy compound is preferred.

The color developing solution used in the present invention is preferably pH 9-1.
2, more preferably 9 to 11.0, and the color developing solution may further contain a compound of a known developing component.

In order to maintain the above pH, it is preferable to use various buffers.

Specific examples of the buffer include sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, trisodium phosphate, tripotassium phosphate, disodium phosphate, dipotassium phosphate, sodium borate, potassium borate,
Sodium tetraborate (borax), potassium tetraborate, o
-Sodium hydroxybenzoate (sodium salicylate), potassium o-hydroxybenzoate, 5-sulfo-
Examples thereof include sodium 2-hydroxybenzoate (sodium 5-sulfosalicylate) and potassium 5-sulfo-2-hydroxybenzoate (potassium 5-sulfosalicylate). However, the invention is not limited to these compounds.

The amount of the buffer to be added to the color developing solution is preferably 0.1 mol / or more, particularly 0.1 mol / to 0.4 mol /.
Is particularly preferred.

In addition, various chelating agents can be used in the color developing solution as an inhibitor of precipitation of calcium or magnesium, or for improving the stability of the color developing solution.

As the chelating agent, an organic acid compound is preferable, and examples thereof include aminopolycarboxylic acids, organic phosphonic acids, and phosphonocarboxylic acids. Specific examples are shown below, but the present invention is not limited thereto.

Nitrilotriacetic acid, diethylenetriaminepentaacetic acid, ethylenediaminetetraacetic acid, N, N, N-trimethylenephosphonic acid, ethylenediamine-N, N, N ', N'-tetramethylenephosphonic acid, transcyclohexanediaminetetraacetic acid,
1,2-diaminopropanetetraacetic acid, hydroxyethyliminodiacetic acid, glycol ether diaminetetraacetic acid, ethylenediamine orthohydroxyphenylacetic acid, 2-phosphonobutane-1,2,4-tricarboxylic acid, 1-hydroxyethylidene-1,1- Diphosphonic acid, N, N'-bis (2-hydroxybenzyl) ethylenediamine-N, N'-diacetic acid.

These chelating agents may be used in combination of two or more as necessary.

These chelating agents may be added in an amount sufficient to block metal ions in the color developing solution. For example, 1
It is about 0.1g to 10g per unit.

An optional development accelerator can be added to the color developing solution as needed. However, it is preferable that the color developing solution of the present invention does not substantially contain benzyl alcohol from the viewpoints of pollution, liquid preparation and prevention of color contamination. Here, “substantially” means that the developer does not contain 2 ml or less, preferably no developer, at all.

Other development accelerators include JP-B-37-16088,
7-5987, 38-7826, 44-12380, 45-9919
No. 3,813,247 and the like, thioether compounds disclosed in JP-A-52-49829 and JP-A-50-15554, p-phenylenediamine-based compounds disclosed in
-137726, JP-B-44-30074, JP-A-56-156826 and JP-A-52-43429, etc., quaternary ammonium salts, U.S. Pat.Nos. 2,494,903, 3,128,182, 4,23
Nos. 0,796, 3,253,919, JP-B-41-11431, U.S. Patent Nos. 2,482,546, 2,596,926 and 3,582,346, etc., and the amine compounds described in JP-B-37-16088, 42-2.
No. 5201, U.S. Pat.No. 3,128,183, JP-B-41-11431,
No. 42-23883 and U.S. Pat.No.3,532,501, polyalkylene oxides and other 1-phenyl-3
-Pyrazolidones, imidazoles and the like can be added as needed.

In the present invention, an optional antifoggant can be added as required. As the antifoggant, alkali metal halides such as sodium chloride, potassium bromide and potassium iodide and organic antifoggants can be used. Examples of organic antifoggants include benzotriazole, 6-
Nitrobenzimidazole, 5-nitroisoindazole, 5-methylbenzotriazole, 5-nitrobenzotriazole, 5-chloro-benzotriazole, 2-
Representative examples include nitrogen-containing heterocyclic compounds such as thiazolyl-benzimidazole, 2-thiazolylmethyl-benzimidazole, indazole, hydroxyazaindolizine, and adenine.

The color developer used in the present invention may contain a fluorescent whitening agent. As the fluorescent whitening agent, a 4,4'-diamino-2,2'-disulfostilbene compound is preferable. The addition amount is 0 to 5 g / preferably 0.1 g to 4 g /.

Further, various surfactants such as alkyl sulfonic acid, aryl sulfonic acid, aliphatic carboxylic acid and aromatic carboxylic acid may be added as needed.

The processing temperature of the color developing solution of the present invention is preferably from 20 to 50 ° C.
30-45 ° C. Processing time is 20 seconds to 5 minutes, preferably 1 minute
30 seconds to 4 minutes. While replenishing amount is desirably small, the photosensitive material 1 m ² per 100～2000Ml, preferably 200～1500Ml. More preferably, it is 300 ml to 1000 ml.

Further, the color developing bath may be divided into two or more baths as necessary, and a color developing replenisher may be replenished from the first bath or the last bath to shorten the developing time and reduce the replenishing amount.

The processing method of the present invention can also be used for color reversal processing. The black-and-white developing solution used at this time is a so-called black-and-white first developing solution which is generally used for reversal processing of a color photosensitive material. Various well-known additives used in a black-and-white developing solution used in a processing solution for a black-and-white silver halide light-sensitive material are added to a black-and-white primary color reversal photosensitive material.
It can be contained in a developer.

Representative additives include developing agents such as 1-phenyl-3-pyrazolidone, methol and hydroquinone, preservatives such as sulfites, and accelerators composed of alkalis such as sodium hydroxide, sodium carbonate and potassium carbonate. , Potassium bromide, 2-methylbenzimidazole,
Examples include inorganic or organic inhibitors such as methylbenzthiazole, water softeners such as polyphosphate, and development inhibitors comprising a small amount of iodide or a mercapto compound.

In the present invention, a used color developing solution (overflow solution) contains a regenerating agent and is reused as a color developing replenisher.

The regenerating agent is added to a used color developing solution (overflow solution) in principle for the purpose of supplementing the components consumed in the color developing process.

The regenerating agent for a color developing replenisher used in the present invention includes, as a rule, a color developing agent, a pH buffering agent and a chelating agent of the same type as used in the color developing solution, and other components as necessary, such as preservatives. It is preferable to contain an agent, a development accelerator, a fluorescent whitening agent and the like. What is necessary is just to set the amount of these chemical | medical agents to the amount which supplements the consumed component. The amount of these regenerants added depends on the resulting regenerating correction solution 1
Per color developing agent is 0.001 to 0.02 mol, pH buffer is 0.0
It is preferable that 1 to 0.2 mol, the chelating agent is 0.001 to 0.02 mol, and the preservative is 0.01 to 0.03 mol.

In the present invention, it is preferable to prevent evaporation of the liquid and air oxidation by reducing the contact area of the processing tank with the air. Concentration can be corrected by adding water as needed when preparing a color developing replenisher for the evaporation of the solution in the developing bath, if necessary.

In the present invention, desilvering is performed after color development. Representative desilvering steps are shown below, but are not limited thereto.

1. (Color development)-Bleaching-Fixing 2. (〃)-Bleaching and fixing 3. (〃)-Bleaching-Bleaching and fixing 4. (〃)-Fixing-Bleaching and fixing 5. (〃)-Bleaching-Bleaching and fixing-Fixing 6. (〃) -Bleaching-fixing-Bleaching 7. (〃) -Bleaching-fixing-fixing If the above desilvering step comprises two or more steps, a washing or rinsing bath may be provided between both steps. Adjustment, washing or a stop bath may be provided between the color developing step and the desilvering step.

In the above-mentioned processing steps, each of the bleaching, bleach-fixing and fixing processing baths may be a single bath, or may be composed of two or more baths. The method of replenishing each processing bath is usually a method of replenishing the replenisher of each processing bath to the corresponding processing bath.However, when the bleach-fix bath comprises a plurality of processing baths, the replenisher is added to the final bath. May be replenished by a so-called countercurrent method of leading the overflow liquid to the pre-bath,
Further, a replenisher may be added to the first bath, and the overflow may be replenished by a so-called forward flow method in which the overflow solution is guided to a subsequent bath. In the steps 3 and 4, the overflow solution of the bleaching bath or the fixing bath, which is the pre-bath, may be introduced into the bleach-fixing bath to replenish the fixing component or the bleaching component in the bleach-fixing bath. In step 5, the overflow solution of the bleaching bath and the overflow solution of the fixing bath may be respectively led to the bleach-fixing bath. In Steps 6 and 7, the components of the subsequent bleaching bath or fixing bath may be led to the bleach-fixing solution.

Examples of the bleaching agent for the bleaching bath or bleach-fixing bath of the present invention include polyvalent transition metal ion compounds such as iron (III), cobalt (IV), chromium (VI), manganese (VII), and copper (II); Substances, quinones, nitrobenzenes and the like are used. For example, ferricyanide dichromate, iron (II
Organic acid chelate compounds of I) or cobalt (IV), ferric chloride, persulfate, hydrogen peroxide, permanganate, benzoquinone, and the like can be used. Among these compounds, it is preferable to use a ferric organic acid complex salt from the viewpoints of pollution, safety and the like, and it is particularly preferable to use a ferric aminopolycarboxylic acid complex salt. These aminopolycarboxylic acids and examples thereof include the above compounds.

1. Ethylenediaminetetraacetic acid 2. Diethylenetriaminepentaacetic acid 3. Cyclohexanediaminetetraacetic acid 4.1,2-propylenediaminetetraacetic acid 5. Ethylenediamine-N- (β-oxyethylel) -N,
N ', N'-triacetic acid 6.1,3-diaminopropanetetraacetic acid 7.1,4-diaminobutanetetraacetic acid 8.glycol ether diaminetetraacetic acid 9.iminodiacetic acid 10.N-methyl-iminodiacetic acid 11.ethylenediaminetetrapropion Acid 12.N- (2-acetamido) iminodiacetic acid 13.Dihydroxyethyl glycine 14.Ethylenediamine di-hydroxyphenylacetic acid Ferric aminopolycarboxylic acid complex salt may be used in the form of a complex salt or a ferric salt. For example, ferric sulfate, ferric chloride, ferric nitrate, ferric ammonium sulfate, ferric phosphate and the like, and a ferric ion complex salt may be formed in a bath using an aminopolycarboxylic acid. Good. When used in the form of a complex salt, one kind of complex salt may be used, or two or more kinds of complex salts may be used. On the other hand, when a complex salt is formed in a solution using a ferric salt and an aminopolycarboxylic acid, one or more ferric salts may be used. Further, one or more aminopolycarboxylic acids may be used. In any case, the aminopolycarboxylic acid may be used in excess of forming a ferric ion complex salt.

Further, the bleaching solution or the bleach-fixing solution containing the above-mentioned ferric ion complex may contain a metal ion complex salt such as iron and iron cobalt.

The amount of these bleaching agents added is preferably 0.05 mol to 1 mol per bleaching solution or bleach-fixing solution.
In particular, it is preferably from 0.1 mol to 0.5 mol.

The bleaching solution or bleach-fixing solution of the present invention may contain a rehalogenating agent such as a bromide, for example, potassium bromide, sodium bromide, ammonium bromide, or a chloride, for example, potassium chloride, sodium chloride, ammonium chloride. . In addition, sodium nitrate, nitrates such as ammonium nitrate, boric acid, borax, sodium metaborate, acetic acid, sodium acetate, sodium carbonate, potassium carbonate, phosphorous acid, phosphoric acid, sodium phosphate, citric acid, sodium citrate,
It may contain one or more inorganic acids, organic acids and salts thereof having pH buffering capacity such as tartaric acid.

A bleaching accelerator can be used in the bleaching solution, the bleach-fixing solution and their prebaths, if necessary. Specific examples of useful bleach accelerators are described in the following specification: U.S. Pat. No. 3,893,858, West German Patent 1,290,812, and 2,059,98.
No. 8, JP-A-53-32,736, JP-A-53-57,831, JP-A-53-37,
No. 418, No. 53-72,623, No. 53-95,630, No. 53-95, 63
No. 1, 53-104,232, 53-124,424, 53-141,6
No. 23, No. 53-28,426, Research Disclosure
Compounds having a mercapto group or a disulfide group described in No. 17,129 (July 1978);
No. 129 thiazolidine derivative; JP-B-45-8,506
No., JP-A-52-20832, JP-A-53-32,735, U.S. Pat.
Thiourea derivatives described in 3,706,561; West German Patent No. 1,12
7,715, iodide salts described in JP-A-58-16,235; polyoxyethylene compounds described in West German Patents 966,410 and 2,748,430; polyamine compounds described in JP-B-45-8836; -42,434, 49-59,644, 53
-94,927, 54-35,727, 55-26,506, 58-
Compounds described in 163,940 can be used. Among them, compounds having a mercapto group or a disulfide group are preferable in view of a large accelerating effect, and in particular, US Patent No. 3,893,858
And compounds described in West German Patent No. 1,290,812 and JP-A-53-95,630. Further, the compounds described in U.S. Pat. No. 4,552,834 are also preferable. These bleaching accelerators may be added to the light-sensitive material. These bleaching accelerators are particularly effective when bleach-fixing color photographic materials for photography.

Examples of the fixing material of the bleach-fixing solution include thiosulfates, thiocyanates, thioether-based compounds, thioureas, and a large amount of iodide, and thiosulfates are generally used. Ammonium sulfate can be used most widely. As a preservative of the bleach-fix solution, it is preferable to use a sulfite, a bisulfite, a carbonyl bisulfite adduct or a sulfinic acid compound.

The pH of the bleaching solution or bleach-fixing solution of the present invention is not particularly limited, but is preferably 3.0 to 8.0 when a ferric aminopolycarboxylic acid complex salt is used as the bleaching agent. The replenishment rate of the bleaching solution or bleach-fixing solution of the present invention, it is necessary to change depending on the amount of coated silver to be processed photographic material, 1000 ml are preferable from the photosensitive material 1 m ² per 10 ml.

The processing method of the present invention comprises the above-described processing steps such as color development, bleaching, bleach-fixing and fixing. here,
After the bleach-fixing or fixing step, processing steps such as washing and stabilization are generally performed. However, after a bath having a fixing ability, a simple stabilization treatment without substantial washing is performed. Processing methods can also be used.

Known additives can be added to the washing water used in the washing step, if necessary. For example, water softeners such as inorganic phosphoric acid, aminopolycarboxylic acid, and organic phosphoric acid, fungicides that prevent the growth of various bacteria and algae, and deterrents (eg, isothiazolone, organochlorine fungicides, benzotriazole, etc.) , A drying load, and a surfactant for preventing unevenness can be used. Also, LEWe
st, “Water Quality Criteria”, Phot.Sci.and Eng., v
ol. 9, No. 6, pages 344 to 359 (1965) and the like can also be used.

As a stabilizing solution used in the stabilizing step, a processing solution for stabilizing a dye image is used. For example, a liquid having a buffer capacity of pH 3 to 6, a liquid containing an aldehyde (for example, formalin), or the like can be used. The stabilizing solution may contain, if necessary, an ammonium compound, a metal compound such as Bi or Al, a fluorescent brightener, a chelating agent (eg, 1-hydroxyethylidene-1,1-diphosphonic acid), a bactericide, a deterrent agent, Hardening agents, surfactants, alkanolamines and the like can be used.

In the washing step and the stabilizing step, a multi-stage countercurrent system is preferable, and the number of stages is preferably two to four. The replenishing amount is 1 to 50 times, preferably 2 to 30 times, more preferably 2 to 15 times the amount brought in from the previous bath per unit area.

Water used in these washing or stabilizing steps is not limited to tap water, and may be C
a, It is preferable to use water deionized to an Mg concentration of 5 mg / or less, water that has been sterilized by halogen, an ultraviolet germicidal lamp, or the like.

In the above processing steps of the color light-sensitive material, when continuous processing is performed by an automatic developing machine, the processing solution may be concentrated due to evaporation, particularly when the processing amount is small or when the opening area of the processing solution is large. Will be noticeable. In order to correct such concentration of the processing solution, it is preferable to replenish an appropriate amount of water or a correction solution.

In addition, the amount of waste liquid can also be reduced by using a method in which the overflow solution in the washing step or the stabilization step is flowed into a bath having a fixing ability, which is a pre-bath.

The light-sensitive material of the present invention only needs to have at least one layer of a silver halide emulsion layer of a blue-sensitive layer, a green-sensitive layer and a red-sensitive layer on a support. There is no particular limitation on the number and order of the emulsion layers and the non-light-sensitive layers. A typical example is a silver halide photographic material having a light-sensitive layer comprising a plurality of silver halide emulsion layers having substantially the same color sensitivity but different sensitivities on a support, The photosensitive layer is a unit photosensitive layer having color sensitivity to any of blue light, green light, and red light, and in a multilayer silver halide color photographic material, the arrangement of the unit photosensitive layers is generally The red-sensitive layer, the green-sensitive layer, and the blue-sensitive layer are provided in this order from the support side. However, the order of installation may be reversed depending on the purpose, or the order of installation may be such that different color-sensitive layers are sandwiched between the same color-sensitive layers.

Non-photosensitive layers such as various intermediate layers may be provided between the silver halide photosensitive layers and as the uppermost layer and the lowermost layer.

The intermediate layer is described in JP-A-61-43748 and JP-A-59-113438.
No. 59-113440, No. 61-20037, couplers as described in the specification of No. 61-20038, DIR compounds and the like may be included, and as commonly used, a color mixing inhibitor, ultraviolet rays It may contain an absorbent or a stain inhibitor.

A plurality of silver halide emulsion layers constituting each unit photosensitive layer are described in West German Patent No. 1,121,470 or British Patent No. 923,045.
No. 2 of the high-speed emulsion layer and the low-speed emulsion layer
A layer configuration can be preferably used. Usually, it is preferable to arrange them so that the light sensitivity decreases sequentially toward the support, and a non-photosensitive layer may be provided between the respective halogen emulsion layers. Also, JP-A-57-112751, 62
No. 200350, No. 62-206541, No. 62-206543, a low-speed emulsion layer on the side away from the support as described in
A high-sensitivity emulsion layer may be provided on the side close to the support.

As specific examples, from the farthest side from the support, a low-sensitivity blue-sensitive layer (BL) / a high-sensitivity blue-sensitive layer (BH) / a high-sensitivity green-sensitive layer (GH) / a low-sensitivity green-sensitive layer (GL) / High-sensitivity red-sensitive layer (RH) / low-sensitivity red-sensitive layer (RL) or BH / BL /
They can be installed in the order of GL / GH / RH / RL or BH / BL / GH / GL / RL / RH.

Also, as described in JP-B-55-34932, the blue-sensitive layer / GH / RH / GL / RL is selected from the side farthest from the support.
Can be arranged in this order. JP-A-56-25738
As described in JP-A-62-63936, the layers may be arranged in the order of blue-sensitive layer / GL / RL / GH / RH from the side farthest from the support.

As described in JP-B-49-15495, the upper layer is the most sensitive silver halide emulsion layer, the middle layer is the less sensitive silver halide emulsion layer, and the lower layer is more sensitive than the middle layer. An example is an arrangement in which a silver halide emulsion layer having a low degree of sensitivity is arranged and three layers having different sensitivities are sequentially reduced in sensitivity toward a support. Even in the case of three layers having different sensitivities, Japanese Patent Laid-Open No.
As described in JP-A-202464, a medium-speed emulsion layer / a high-speed emulsion layer / a low-speed emulsion layer may be arranged in the same color-sensitive layer from the side away from the support.

As described above, various layer configurations and arrangements can be selected according to the purpose of each photosensitive material.

Any of these layer arrangements can be used in the color light-sensitive material of the present invention.

Swelling ratio in the photosensitive material of the present invention [(equilibrium swelling film thickness in 25 ° C., H ₂ O−25 ° C., dry film thickness at 55% RH / 25 ° C., 55% R
(Dry total film thickness in H) × 100] is preferably 50 to 200%,
~ 150% is more preferred. If the swelling ratio deviates from the above value, photographic properties are liable to change.

Further, the swelling speed in the light-sensitive material of the present invention is defined as a swelling speed T 1/2 in which half of the time required to reach 90% of the saturated swelling film thickness in a color developing solution (38 ° C.) is defined. , T 1 /
2 is preferably 15 seconds or less. More preferably T 1/2
Is less than 9 seconds.

The photographic emulsion layer of the color light-sensitive material used in the present invention is approximately
Silver iodobromide containing 80 mol% or more of silver bromide. Particularly preferred is silver iodobromide containing from about 98 mol% to about 90 mol% complaints.

Silver halide grains in photographic emulsions are cubic, octahedral,
It may be one having regular crystals such as tetradecahedron, one having irregular crystal forms such as spherical or plate-like, one having crystal defects such as twin planes, or a complex form thereof.

The silver halide may be fine grains having a grain size of about 0.2 μm or less or large grains having a projected area diameter of about 10 μm, and may be a polydisperse emulsion or a monodisperse emulsion.

The silver halide photographic emulsion usable in the present invention is described, for example, in Research Disclosure (RD), No. 17643 (1978).
December, p. 22-23, "I. Emulsion preparat
ion and types) ”and No. 18716 (November 1979
Mon), p.648, Grafkid, "Physics and Chemistry of Photography", published by Paul Montell (P. Glafkides, Chemic et Phisique P
hotographique Paul Mantel, 1967), "Photographic Emulsion Chemistry" by Duffin, published by Focal Press (GFDuffin Photo).
graphic Emulsion Chemistry (Focal Press, 1966) ",
"Manufacture and Coating of Photographic Emulsions", by Zelikman et al., Published by Focal Press (VLZelikman et al. Making and Coating).
Photographic Emulsion, Focal Press, 1964).

Monodisperse emulsions described in U.S. Pat. Nos. 3,574,628 and 3,655,394 and British Patent 1,413,748 are also preferable.

Tabular grains having an aspect ratio of about 5 or more can also be used in the present invention. Tabular grains are provided by Gaft, Gutoff, PhotogrPhic Science and Engineerin.
g), 14, 248-257 (1970); U.S. Pat.
4,226, 4,414,310, 4,433,048, 4,439,520
And British Patent No. 2,112,157.

The crystal structure may be uniform, the inside and the outside may be composed of different halogen compositions, or may have a phase structure.Also, silver halides having different compositions are joined by epitaxial junction. And it may be bonded to a compound other than silver halide such as, for example, silver rhodan and lead oxide.

 Also, a mixture of particles of various crystal forms may be used.

In the present invention, it is particularly preferable that the coated silver amount of the light-sensitive material is 2 to 6 g / m ² .

As the silver halide emulsion, usually, those subjected to physical ripening, chemical ripening and spectral sensitization are used. The additive used in such a process is Research Disclosure No. 1
7643 and No. 18716, and the relevant portions are summarized in the table below.

Known photographic additives that can be used in the present invention are also described in the above two Research Disclosures, and the relevant portions are shown in the following table.

Various color couplers can be used in the present invention, and specific examples are described in the above-mentioned patents described in RD No. 17643, VII-CG.

As a yellow coupler, for example, U.S. Pat.
No. 501, No. 4,022,620, No. 4,326,024, No. 4,401,752
No. 4,248,961; Japanese Patent Publication No. 58-10739; British Patent No. 1,
425,020, 1,476,760, U.S. Pat.No. 3,973,968,
Preferred are those described in JP-A-4,314,023 and JP-A-4,511,649 and European Patent No. 249,473A.

As the magenta coupler, 5-pyrazolone-based and pyrazoloazole-based compounds are preferable, and US Patent No. 4,310,
Nos. 6,19,4,351,897, EP 73,636, U.S. Pat.
), JP-A-60-43659, JP-A-61-72238, and JP-A-60-3573.
No. 5, No. 51-118034, No. 60-185951, U.S. Pat.
00,630, 4,540,654, 4,556,630, WO (PCT) 8
What is described in 8/04795 etc. is especially preferable.

Examples of cyan couplers include phenol-based and naphthol-based couplers, and are described in U.S. Pat.
4,146,396, 4,228,233, 4,296,200, 2,36
9,929, 2,801,171, 2,772,162, 2,895,826
No. 3,772,002, No. 3,758,308, No. 4,334,011,
No. 4,327,173, West German Patent Publication No. 3,329,729, European Patent Nos. 121,365A and 249,453A, U.S. Patent No. 3,446,622
No. 4,333,999, 4,753,871, 4,451,559,
4,427,767, 4,690,889, 4,254,212, 4,2
Nos. 96,199 and JP-A-61-42658 are preferred.

Colored couplers for correcting unwanted absorption of coloring dyes are described in RD No. 17643, Section VII-G, U.S. Pat.
No. 70, Japanese Patent Publication No. 57-39413, U.S. Pat.No. 4,004,929,
Those described in 4.138,258 and British Patent 1,146,368 are preferred. Further, a coupler that corrects unnecessary absorption of a coloring dye from a fluorescent dye released at the time of coupling described in U.S. Pat.No. 4,774,181 and a dye that can form a dye by reacting with a developing agent described in U.S. Pat.No. 4,777,120 It is also preferable to use a coupler having a precursor group as a leaving group.

As a coupler in which the coloring dye has an appropriate diffusivity,
Preferred are those described in U.S. Pat. No. 4,366,237, British Patent No. 2,125,570, European Patent No. 96,570, and West German Patent (Published) No. 3,234,533.

Typical examples of polymerized dye-forming couplers are U.S. Patent Nos. 3,451,820; 4,080,211; 4,367,282;
No. 4,409,320, No. 4,576,910, UK Patent No. 2,102,173
No. etc.

Couplers that release a photographically useful residue upon coupling can also be preferably used in the present invention. DIR couplers that release development inhibitors are described in RD17643, VII-F above.
Patents, JP-A-57-151944 and JP-A-57-1542
No. 34, No. 60-184248, No. 63-37346, U.S. Pat.
Preferred are those described in JP-A-48,962 and JP-A-4,782,012.

Examples of couplers that release a nucleating agent or a development accelerator imagewise during development include UK Patent Nos. 2,097,140 and 2,13.
No. 1,188, JP-A Nos. 59-157638 and 59-170840 are preferred.

Other couplers that can be used in the light-sensitive material of the present invention include competing couplers described in U.S. Patent No. 4,130,427 and the like, U.S. Patent Nos. 4,283,472, 4,338,393, and
4,310,618 etc., multi-equivalent couplers, JP-A-60-185
No. 950, DIR redox compound releasing couplers described in JP-A-62-24252, etc., DIR coupler releasing couplers, DIR coupler releasing redox compounds or DIR redox releasing redox compounds, discoloration after disengagement described in EP 173,302A. RD No.11449, 2
4241, bleach accelerator releasing couplers described in JP-A-61-201247, etc., ligand releasing couplers described in U.S. Pat.No. 4,553,477, etc., couplers releasing leuco dyes described in JP-A-63-75747, U.S.A. Couplers that release a fluorescent dye described in Japanese Patent No. 4,774,181 are exemplified.

The coupler used in the present invention can be introduced into a light-sensitive material by various known dispersion methods.

Examples of high-boiling solvents used in the oil-in-water dispersion method are described in U.S. Patent No. 2,322,027, and specific examples of high-boiling organic solvents having a boiling point at normal pressure of 175 ° C or higher used in the oil-in-water dispersion method Examples include phthalic acid esters (dibutyl phthalate, dicyclohexyl phthalate, di-2-ethylhexyl phthalate, decyl phthalate, bis (2,
4-di-t-amylphenyl) phthalate, bis (2,4-
Di-t-amylphenyl) isophthalate, bis (1,1
-Diethylpropyl) phthalate), esters of phosphoric acid or phosphonic acid (triphenyl phosphate,
Tricresyl phosphate, 2-ethylhexyl diphenyl phosphate, tricyclohexyl phosphate,
Tri-2-ethylhexyl phosphate, tridodecyl phosphate, tributoxyethyl phosphate, trichloropropyl phosphate, di-2-ethylhexyl phenyl phosphonate, etc., benzoic acid esters (2
-Ethylhexyl benzoate, dodecyl benzoate, 2-ethylhexyl-p-hydroxybenzoate and the like, amides (N, N-diethyldodecaneamide, N, N
-Diethyl laurylamide, N-tetradecylpyrrolidone, etc.), alcohols or phenols (isostearyl alcohol, 2,4-di-tert-amylphenol), aliphatic carboxylic acid esters (bis (2-ethylhexyl) sebacate) , Dioctyl azelate, glycerol tributyrate, isostearyl lactate,
Trioctyl citrate), aniline derivatives (N, N
-Dibutyl-2-butoxy-5-tert-octylaniline), hydrocarbons (paraffin, dodecylbenzene, diisopropylnaphthalene, etc.) and the like. As the auxiliary solvent, an organic solvent having a boiling point of about 30 ° C. or higher, preferably 50 ° C. or higher and about 160 ° C. or lower can be used,
Typical examples include ethyl acetate, butyl acetate, ethyl propionate, methyl ethyl ketone, cyclohexanone,
Ethoxyethyl acetate, dimethylformamide and the like can be mentioned.

The steps and effects of the latex dispersion method and specific examples of the latex for impregnation are described in U.S. Pat. No. 4,199,363 and West German Patent Application (OLS) Nos. 2,541,274 and 2,541,230.

These couplers may be impregnated with a loadable latex polymer (for example, U.S. Pat.No. 4,203,716) in the presence or absence of the high-boiling organic solvent, or dissolved in a water-insoluble and organic solvent-soluble polymer to form a hydrophilic polymer. It can be emulsified and dispersed in a water-soluble colloid aqueous solution.

Preferably, International Publication No.WO88 / 00723, twelfth
Homopolymers or copolymers described on pages 30 to 30 are used. In particular, use of an acrylamide-based polymer is preferred for stabilizing a color image.

The present invention can be applied to various color light-sensitive materials. In particular, color negative films for general use or movies,
It is preferably applied to a color reversal film for a slide or a television.

Suitable supports that can be used in the present invention include, for example, those described above.
RD. No. 17643, page 28, and RD. No. 18716, page 647, right column, 64
It is described in the left column on page 8.

(Examples) Hereinafter, the present invention will be described in more detail by way of examples, but the present invention is not limited thereto.

Example 1 On an undercoated cellulose triacetate film support, a sample 101, which is a multilayer color photographic material composed of each layer having the following composition, was prepared.

The amount coated amount (Composition of photosensitive layer) is represented in units of g / m ² of silver for silver halide and colloidal silver, also couplers, the amount for the additives and gelatin, expressed in units of g / m ^2, The sensitizing dyes are shown in terms of molarity per mole of silver halide in the same layer.

First layer (antihalation layer) Black colloidal silver 0.15 Gelatin 1.5 ExM-8 0.08 UV-1 0.03 UV-2 0.06 Solv-2 0.08 UV-3 0.07 Cpd-5 … 6 × 10 ^-4 Second layer (intermediate layer) Gelatin… 1.5 UV-1… 0.03 UV-2… 0.06 UV-3… 0.07 ExF-1… 0.004 Solv-2… 0.07 Cpd- 5 6 × 10 ^-4 third layer (first red-sensitive emulsion layer) Silver iodobromide emulsion (AgI 2 mol%, internal high AgI type, equivalent sphere diameter)
0.3 μm, coefficient of variation of equivalent sphere diameter 29%, normal crystal, twin mixed particles, diameter / thickness ratio 2.5) coated silver amount 0.5 gelatin 0.8 ExS-1 1.0 × 10 ^-4 ExS-2 3.0 × 10 ^-4 ExS-3 ...... 1 × 10 ^-5 ExC-3 ...... 0.22 ExC-4 ...... 0.02 Cpd-5 ...... 3 × 10 ^-4 Fourth layer (second red-sensitive emulsion layer) Silver bromide emulsion (AgI 4 mol%, internal high AgI type, equivalent sphere diameter of 0.
55 µm, coefficient of variation of equivalent sphere diameter 20%, normal crystal, twin mixed particles, diameter / thickness ratio 1) Silver coating amount 0.7 gelatin 1.26 ExS-1 1 x 10 ^-4 ExS-2 3 x 10 ^-4 ExS-3 ... 1 x 10 ^-5 ExC-3 ... 0.33 ExC-4 ... 0.01 ExY-16 ... 0.01 ExC-7 ... 0.04 ExC-2 ... 0.08 Solv-1 ... 0.03 Cpd-5 5 × 10 ^-4 Fifth layer (third red-sensitive emulsion layer) Silver iodobromide emulsion (AgI 10 mol%, internal high AgI type, equivalent sphere diameter)
0.7 μm, Coefficient of variation of equivalent sphere diameter 30%, twin mixed grains, diameter / thickness ratio 2) Silver coating amount 0.7 Gelatin 0.8 ExS-1 1 × 10 ^-4 ExS-2 3 × 10 ^-4 ExS-3 ... 1 x 10 ^-5 ExC-5 ... 0.05 ExC-6 ... 0.06 Solv-1 ... 0.15 Solv-2 ... 0.08 Cpd-5 ... 3 x 10 ^-5 6th layer (Intermediate layer) Gelatin, 1.0 Cpd-5 4 × 10 ^-4 Cpd-1 0.10 Cpd-4 1.23 Solv-1 0.05 Cpd-3 0.25 Seventh layer (first green) Sensitive emulsion layer) Silver iodobromide emulsion (AgI 3 mol%, internal high AgI type, equivalent sphere diameter 0.
3 μm, coefficient of variation of sphere equivalent diameter 28%, normal crystal, twin mixed particles, diameter / thickness ratio 2.5) Coating silver amount 0.30 Gelatin 0.4 ExS-4 5 × 10 ^-4 ExS-6 0.3 × 10 ^-4 ExS-5… 2 × 10 ^-4 ExM-9… 0.2 ExY-14… 0.03 ExM-8… 0.03 Solv-1… 0.2 Cpd-5… 2 × 10 ^-4 Eight layers (second green-sensitive emulsion layer) Silver iodobromide emulsion (AgI 4 mol%, internal high AgI type, equivalent sphere diameter of 0.
55 μm, coefficient of variation of equivalent sphere diameter 20%, normal crystal, twin mixed particles, diameter / thickness ratio 4) Silver coating amount 0.6 gelatin 0.8 ExS-4 5 × 10 ^-4 ExS-5 2 x 10 ^-4 ExS-6 ... 0.3 x 10 ^-4 ExM-9 ... 0.25 ExM-8 ... 0.03 ExM-10 ... 0.015 ExY-14 ... 0.04 Solv-1 ... 0.2 Cpd-5 3 x 10 ^-4 ninth layer (third green-sensitive emulsion layer) Silver iodobromide emulsion (AgI 10 mol%, internal high AgI type, equivalent sphere diameter)
0.7 μm, coefficient of variation of sphere equivalent diameter 30%, normal crystal, twin mixed particles, diameter / thickness ratio 2.0) coated silver amount 0.85 gelatin 1.0 ExS-4 2.0 × 10 ^-4 ExS-5 … 2.0 × 10 ^-4 ExS-6… 0.2 × 10 ^-4 ExS-7… 3.0 × 10 ^-4 ExM-12… 0.06 ExM-13… 0.02 ExM-8… 0.02 Solv-1… 0.20 Solv-2 ... 0.05 Cpd-5 ... 4 x 10 ^-4 10th layer (yellow filter layer) Gelatin ... 0.9 Yellow colloidal silver ... 0.05 Cpd-1 ... 0.2 Solv-1 ... 0.15 Cpd-5 ... … 4 × 10 ^-4 eleventh layer (first blue-sensitive emulsion layer) Silver iodobromide emulsion (AgI 4 mol%, internal high AgI type, equivalent sphere diameter of 0.1%)
5 μm, coefficient of variation of sphere equivalent diameter: 15%, octahedral particles) Silver coating: 0.4 Gelatin: 1.0 ExS-8: 2 x 10 ^-4 ExY-16: 0.9 ExY-14: 0.09 Solv-1 0.3 Cpd-5 4 × 10 ^-4 12th layer (second blue-sensitive emulsion layer) Silver iodobromide emulsion (AgI 10 mol%, internal high AgI type, equivalent sphere diameter)
1.3 μm, coefficient of variation of sphere equivalent diameter 25%, normal crystal, twin mixed particles, diameter / thickness ratio 4.5) Silver coating amount 0.5 Gelatin 0.6 ExS-8 1 × 10 ^-4 ExY-16 0.12 Solv-1 0.04 Cpd-5 2 × 10 ^-4 th layer (first protective layer) Fine grain silver iodobromide (average grain size 0.07 μm, AgI 1 mol%)
… 0.2 Gelatin… 0.8 UV-3… 0.1 UV-4… 0.1 UV-5… 0.2 Solv-3… 0.04 Cpd-5… 3 × 10 ^-4 14th layer (second protective layer) Gelatin …… 0.9 Polymethyl methacrylate particles (1.5μm in diameter) …… 0.2
Cpd-5... 4 × 10 ⁻⁴ H-1... 0.4 In addition to the above components, a surfactant was added to each layer as a coating aid. The sample prepared as described above was used for sample 10
It was set to 1.

Next, the chemical structural formulas or chemical names of the compounds used in the present invention are shown below.

Solv-1: Tricresyl phosphate Solv-2: Dibutyl phthalate Solv-3: Bis (2-ethylhexyl) phthalate The sample 101 obtained as described above was processed to a width of 35 mm and subjected to imagewise exposure.

Next, as described in Examples of JP-A-54-37731, an ion exchange membrane electrodialysis method and a halogen ion concentration adjusting device were installed based on the embodiment shown in FIG.

Next, as shown in FIG. 1, the above-mentioned apparatus was connected to a developing solution tank of an automatic developing machine, an overflow solution of the developing solution was stocked, a regenerant was added, and a system for recycling as a replenishing solution was prepared. Details of the processing are as follows.

Next, the composition of the processing solution used is shown below.

(Stabilizer) Common solution for mother liquor and replenisher (37%) 1.2 ml 5-chloro-2-methyl-4-isothiazolin-3-one 6.0 mg 2-methyl-4-isothiazolin-3-one 3.0 mg surfactant 0.4 [ C ₁₀ H ₂₁ -OCH ₂ CH ₂ O ₁₀ H] Ethylene glycol 1.0 Add water 1.0L pH 5.0-7.0 The ion exchange membrane electrodialysis tank is connected to a desalting room (5 dm ² × 20 room) Was circulated. On the other hand, the developing solution was diluted to 1/4 in a concentration chamber, and a solution 10 to which 4.5 g of potassium bromide was added per 1 was circulated (10 / min). Further, in the anode chamber, platinum-plated titanium was used as the anode, and in the cathode chamber, stainless steel was used as the cathode.
Was circulated.

Electrode solution Sodium carbonate 30 g Sodium bicarbonate 6 g EDTA · 2Na 1 g Water was added to 1 pH 10.20 The overflow solution of the color developer was added to the stock at the time of 75 stocks, and the following chemicals were added to 100, and reused as a replenisher.

Overflow liquid 75 1-hydroxyethylidene-1,1-diphosphonic acid 38 g diethylenetriaminepentaacetic acid 75 g sodium sulfite 250 g potassium carbonate 1450 g hydroxylamine sulfate 200 g 4- [N-ethyl-N-β-hydroxyethylamino] -2-me Chillaniline sulfate 390 g Water was added and the pH was changed to 100 pH 10.15 Next, change the tank solution of the running start solution and the Br ion concentration of the halogen ion concentration adjusting device as shown in Table 1 and start running each, 20 times each. The change in photographic properties before playback was determined.

For the change in photographic properties, a wedge-shaped exposure was applied to Sample 101, and the sample was processed at the start, 5, 10, 15, and 20 times at the end of reproduction, and the photographic change of yellow from the start was obtained.

ΔDmin: change in minimum density ΔS: change in sensitivity, log from Dmin until density increases by 0.1
Table 1 shows the results of the change in the E value, ΔH: the change in gradation, and the change in density on the high exposure side by 0.5 logE from the sensitivity point.

In the Br ion setting level of the present invention (No.
5) Changes in photographic properties due to running are small.
3, 4 is preferred. On the other hand, in No. 1, low feeling and soft tone are accompanied by running, and in No. 6, high feeling and high contrast.

Example 2 Samples 201 to 205 were prepared in the same manner as in Sample 101 except that the silver halide emulsion composition of each layer was changed as follows.

The samples 201 to 205 obtained as described above were subjected to No. 1 and No. 4 treatments of Example 1 in the same manner as in Example 1, respectively.
Table 2 shows the change in the ΔDmin value during running.

According to Table 2, Nos. 16, 17, and 19 containing silver halide emulsions having a Br content of 80 mol% or more (I ^- content of 20 mol% or less) show excellent running performance, Silver emulsion (N
o.20) shows poor performance and increased fog.

(Effects of the Invention) According to the present invention, excellent performance (especially sensitivity and gradation) can be obtained stably in a developing waste liquid regenerating system using an ion exchange membrane electrodialysis method.

Furthermore, when a photosensitive material having a coated silver amount of 2 to 6 g / m ² is used, or when a replenishing amount of the color developing solution is a relatively large replenishing amount of about 200 to 1500 ml / m ² , the photographic properties by running can be improved. Fluctuations are particularly stabilized.

[Brief description of the drawings]

FIG. 1 shows a conceptual diagram for carrying out a specific example of the processing method of the present invention. DESCRIPTION OF SYMBOLS 1 ... Developer tank 2 ... Bleach tank 3 ... Fixer tank 4 ... Washing and / or stabilization processing tank 5 ... Drying zone 11 ... Ion exchange membrane electrodialysis type regenerator 12,13 ... Supply line 14 Water supply line 15 Drain line 16 Drain line 21 Overflow liquid stock tank 22 Liquid preparation tank 23 Replenisher stock tank 24 Regenerant storage tank

Claims (2)

(57) [Claims] 1. A method for processing a silver halide color photographic light-sensitive material by regenerating a color developing solution by an ion exchange membrane electrodialysis method using an anion exchange membrane and a cation exchange membrane. The photographic material has at least one silver iodobromide emulsion layer having a silver bromide content of 80 mol% or more.
Layer, the equilibrium concentration of bromine ions in the developer is 6.0 × 10 ^-3
~ 1.3 × 10 ^-2 mol / at a constant concentration, and the replenishment amount of the color developing solution is 200 per m ^{2 of the} photosensitive material.
A method for processing a silver halide color photographic light-sensitive material, wherein the amount is from 1500 to 1500 ml. 2. The processing method according to claim 1, wherein the amount of silver applied to the silver halide color photographic light-sensitive material is 2 to 6 g / m ² .