Color image-stabilization processing solution used for processing a silver halide color photographic material and a processing method using the same

FIELD OF THE INVENTION
The present invention relates to a color image stabilization processing solution used for processing a silver halide color photographic material (hereinafter referred to as a light-sensitive material) and a processing method therewith, particularly to a stabilization processing solution which contains formaldehyde having a reduced vapor pressure and can provide a dye image having an excellent stability and to a processing method therewith.
BACKGROUND OF THE INVENTION
In general, the fundamental steps for processing a color light-sensitive material are the color developing step and the desilvering step. In the color developing step, exposed silver halide is reduced with a color developing agent to generate silver and the oxidation developing agent reacts with a coupler to form a dye image. In the subsequent desilvering step, silver formed in the developing step is oxidized by the action of an oxidizing agent generally called a bleaching agent and is then dissolved with an agent for forming a complex ion of a silver ion, which is generally called as a fixing agent. After going through this desilvering step has been performed, only the dye images are formed on the color light-sensitive material.
Usually, after these steps, a washing processing is carried out to remove an unnecessary processing solution drainage.
In the case of a color paper and a reversal color paper, the processing is finished with the above steps and a drying step generally follows. In the processing of a color negative film and a reversal color film, a stabilizing step is necessary in addition to the above steps. It is well known that the stabilizing bath in the final step following these processing steps contains formaldehyde for the purpose of preventing fading of the magenta dye attributable to the magenta coupler remaining in the light-sensitive material after processing. A small quantity of formaldehyde vapor is generated when the stabilizing bath containing formaldehyde is prepared and a light-sensitive material having a stabilizing solution attached thereon is dried.
It is known that the inhalation of formaldehyde is harmful for the human body and the Japan Association of Industrial Health advises that the allowable concentration of formaldehyde in a working environment is 0.5 ppm. Therefore, the effort to reduce the concentration of formaldehyde in the stabilizing bath and replace formaldehyde with an alternative has been made to improve the working environment.
A hexamethylenetetramine compound is described in, for example, JP-A-63-244036 (the term "JP-A" as used herein means an unexamined published Japanese patent application), as an alternative for formaldehyde. The use of this compound reduces the concentration of formaldehyde, that is, the vapor pressure of formaldehyde, but it also restricts the desired anti-fading function of a magenta dye and causes a marked fading within several weeks even at room temperature.
On the other hand, many N-methylol compounds having the specific structure have been proposed. For example, U.S. Pat. Nos. 2,487,569 and 2,629,660 disclose N-methylol compounds of melamines; U.S. Pat. No. 2,579,435 discloses N-methylol compounds of urea or 2-oxapropylene urea; U.S. Pat. No. 2,487,446 and JP-B-45-8506 disclose N-methylol compounds of thiourea compounds; U.S. Pat. No. 2,579,436 and British Patent 684,540 disclose N-methylol compounds of hydantoins; British Patent 908,136 discloses N-methylol compounds of cyandiamides; U.S. Pat. No. 3,801,322 and JP-A-61-35447 disclose N-methylol compounds of guanidines; British Patent 1,392,134 discloses N-methylol compounds of morpholine or biuret compounds; and JP-A-2-153348 discloses N-methylol compounds of pyrrole, pyrrolidine, methylamine, glycine, or ethylcarbamate. Further, the methods for using these compounds have also been proposed in, for example, U.S. Pat. Nos. 4,786,583, 4,859,574, and 4,921,779 and European Patents 345,172A and 395,442A.
However, of these compounds, those having the reduced vapor pressure of formaldehyde as compared with formaldehyde itself are poor in the image preservability, and those having the improved image preservability only have the same vapor pressure of formaldehyde as formaldehyde itself. These compounds can not have both the effect of improving the image preservability and the reduction of vapor pressure of formaldehyde.
Also, it has been found that these compounds cause the formation of stain, the deterioration of preservability of a yellow or cyan dye or other dyes contained in the light-sensitive material, and the reduction of solubility although the image preservability of a magenta dye is improved, and there is the problem that these compounds stick to the light-sensitive material and stain the processed image.
Therefore, there has been a strong demand for a compound having a sufficient anti-fading function to a magenta dye and the low formaldehyde vapor pressure, that is, for an effective alternative for formaldehyde.
SUMMARY OF THE INVENTION
One object of the present invention is to provide a color image-stabilization processing solution which does not substantially release the compounds harmful to the human body.
A second object of the present invention is to provide a color image-stabilization processing solution which can provide a color image which is safe and is excellent in the image preservability of a light-sensitive material after processing and a processing method using the same.
A third object of the present invention is to provide a color image-stabilization processing solution which can provide a color image having a superior image preservability and causes no problems such as stain of a light-sensitive material and a processing method using the same.
These and other objects of the present invention have been achieved by:
(1) a color image-stabilization processing solution for a silver halide color photographic material containing at least one of (a) an N-methylol compound represented by the following formula (I): ##STR2## wherein X represents a group of non-metallic atoms necessary to form a 1H-pyrazole ring or 1H-1,2,4-triazole ring together with the nitrogen atom;
and (b) an N-methylol compound satisfying the condition that an equilibrium constant in water at room temperature is 2.times.10.sup.-2 mol/liter or less and a formaldehyde-releasing rate constant is 1.times.10.sup.-1 sec.sup.-1 or more (hereinafter referred to as condition (A)), and
(2) a method for processing an image-wise exposed silver halide color photographic material, which comprises processing the photographic material with a color image-stabilization processing solution and/or color image-stabilization processing replenishing solution containing at least one of the N-methylol compound of formula (I) and the compound satisfying condition (A).

DETAILED DESCRIPTION OF THE INVENTION
The color image-stabilization processing solution of the present invention containing the N-methylol compound of the present invention can provide a working environment in which formaldehyde vapor pressure is reduced. (The "N-methylol compound of the present invention" as used herein includes both the compound of formula (I) and the compound satisfying condition (A).) Further, the present invention is largely characterized by the fact that a dye image can be stabilized by processing a light-sensitive material with a color image-stabilization processing solution containing the N-methylol compound of the present invention without using formaldehyde. Accordingly, in the present invention, any processing step, processing method, processing solution and light-sensitive material can be used as long as the color image-stabilization processing solution of the present invention is used.
The N-methylol compounds represented by formula (I) will be explained in more detail.
The pyrazole ring or 1,2,4-triazole ring formed by X may be substituted or unsubstituted. Further, where the pyrazole ring formed by X has at least two or more substituents, the substituents which are in the ortho position to each other may combine with each other to form a 5- to 7-membered ring.
Of the N-methylol compounds represented by formula (I), preferred are the compounds satisfying condition (A).
Of the N-methylol compounds represented by formula (I), further preferred are the compounds represented by the following formula (Ia): ##STR3## wherein Za represents --N.dbd., --CH.dbd. or --C(R.sub.2).dbd.; R.sub.1, R.sub.2 and R.sub.3 may be the same or different, and each represents a hydrogen atom, an alkyl group, an alkenyl group, an aryl group, a heterocyclic group, a halogen atom, a nitro group, a cyano group, a sulfo group, a carboxyl group, a phospho group, an acyl group, a sulfonyl group, a sulfinyl group, an acyloxy group, an alkoxycarbonyl group, a carbamoyl group, a sulfamoyl group, an amino group, or --Y--Ra, in which Y represents an oxygen atom or a sulfur atom, and Ra represents an alkyl group, an alkenyl group, an aryl group or a heterocyclic group; the above groups may be further substituted with the above groups, a hydroxy group, etc.; and R.sub.1 and R.sub.2 or R.sub.2 and R.sub.3 may combine with each other to form a 5- to 7-membered ring.
More specifically, in formula (Ia) R.sub.1, R.sub.2 and R.sub.3 each represents a hydrogen atom, an alkyl group (for example, methyl, ethyl, n-propyl, butyl, cyclopropyl, hydroxymethyl and methoxymethyl), an alkenyl group (for example, allyl), an aryl group (for example, phenyl and 4-tert-butylphenyl), a heterocyclic group (for example, 5-pyrazolyl and 4-pyrazolyl), a halogen atom (for example, chlorine, fluorine and bromine), a nitro group, a cyano group, a sulfo group, a carboxyl group, a phospho group, an acyl group (for example, acetyl, benzoyl and propanoyl), a sulfonyl group (for example, methanesulfonyl, octanesulfonyl and toluenesulfonyl), a sulfinyl group (for example, methanesulfinyl), an acyloxy group (for example, acetoxy), an alkoxycarbonyl group (for example, methoxycarbonyl and butoxycarbonyl), a carbamoyl group (for example, carbamoyl and N-ethylcarbamoyl), a sulfamoyl group (for example, sulfamoyl and N-ethylsulfamoyl), an amino group (for example, amino, diethylamino, acetylamino, methanesulfonamino, methylureido, N-methylsulfamoylamino, and methoxycarbonylamino), an alkoxy group (for example, methoxy and ethoxy), an alkylthio group (for example, methylthio and octylthio), an aryloxy group (for example, phenoxy), an arylthio group (for example, phenylthio), a heterocyclicoxy group (for example, 1-phenyltetrazole-5-oxy), and a heterocyclic thio group (for example, benzothiazolylthio).
In formula (Ia), preferred R.sub.1, R.sub.2 and R.sub.3 are independently a hydrogen atom, an alkyl group, an alkenyl group, a halogen atom, a sulfo group, a carboxyl group, an acyloxy group, an amino group, an alkoxy group and an alkylthio group, and a hydrogen atom, an alkyl group, a halogen atom, an acyloxy group, an amino group, an alkoxy group and an alkylthio group are more preferred, and a hydrogen atom, an alkyl group, an amino group, an alkoxy group and an alkylthio group are most preferred.
From the view,point of the heat-fading property of a cyan image or the prevention of a yellow stain, preferred are the compounds in which R.sub.1, R.sub.2 and R.sub.3 in formula (Ia) are independently a hydrogen atom or an unsubstituted alkyl group having 1 to 3 carbon atoms, more preferred are the compounds in which at most one of R.sub.1, R.sub.2 and R.sub.3 is a methyl group and the others are the hydrogen atom, and particularly preferred are the compounds in which all of them are the hydrogen atoms.
The dissolution of the N-methylol compound of the present invention in water at room temperature (about 25.degree. C.) causes the following reaction to reach an equilibrium: ##STR4## kr: a formaldehyde-releasing rate constant kf: a generation speed of an N-methylol compound
K: an equilibrium constant defined by: ##STR5##
K in the above reaction shows the equilibrium constant defined by the present invention. Further, kr in the above reaction shows the formaldehyde-releasing rate constant defined by the present invention. In the present invention, "in water" includes heavy water in addition to the conventionally used water.
The equilibrium constant can be obtained by measuring the heavy water solution in which the N-methylol compound of the present invention is dissolved or the heavy water solution containing an amine compound and formaldehyde (37% formalin aqueous solution) in the equimolar amounts each other with a nuclear magnetic resonance absorption method (NMR) and calculating from a proton ratio at the moment the components generated in the solution when the peak variation of NMR was not observed.
The formaldehyde-releasing rate constant kr was obtained in the following manner: formaldehyde and an amine compound were added to water or hearty water at a room temperature and the amounts of the N-methylol compound, formaldehyde and amine compound were observed over time until they reached the equilibrium to obtain the generation speed constant kf of the N-methylol compound; and the constant kf thus obtained was multiplied by the above equilibrium constant K to calculate the formaldehyde-releasing rate constant kr. The compound can be detected by a nuclear magnetic resonance absorption method, an ultraviolet or visible radiation spectroscopic method, high performance liquid chromatography, or a calorimetric quantitative method, and the means for the detection can be appropriately selected depending on the degree of reaction rate.
Further, the equilibrium constant K is 2.times.10.sup.-2 mol/liter or less, preferably 1.5.times.10.sup.-2 mol/liter or less, and more preferably 1.times.10.sup.-2 mol/liter or less. The formaldehyde releasing rate constant kr is 1.times.10.sup.-5 sec.sup.-1 or more, preferably 1.times.10.sup.-4 sec.sup.-1 or more, further more preferably 1.times.10.sup.-3 sec.sup.-1 or more and most preferably 1.times.10.sup.-2 sec.sup.-1 or more.
The N-methylol compound satisfying condition (A) of the present invention includes, for example, an N-methylol product of pyrazole, an N-methylol product of 1,2,4-triazole, and an N-methylol product of urazole.
The compound satisfying condition (A) of the present invention preferably has a cyclic nitrogen-containing heterocyclic amine compound as structure of the amine compound to be released and the cyclic nitrogen-containing heterocyclic amine compound preferably has an aromatic ring or keto or ketoid structure of an aromatic ring.
Of the compounds satisfying condition (A) of the present invention, further preferred are the compounds represented by the following formula (III): ##STR6## wherein Zb represents a group of non-metallic atoms necessary to form a 4- to 8-membered ring, provided that the atom to be bonded to the nitrogen atom is an atom selected from a carbon atom, an oxygen atom or a sulfur atom.
The ring formed by Zb may have a substituent. Further, the ring formed by Zb may be condensed by an aromatic ring, an aliphatic ring or a hetero ring or may be a spiro ring. The substituents that the ring formed by Zb may have include those of R.sub.1 in formula (Ia). Of these, compounds which are not condensed by a benzene ring are preferred as the compounds represented by formula (III), because the compounds which are condensed by a benzene ring have a low solubility.
In the N-methylol compounds satisfying condition (A) of the present invention, more preferred are the N-methylol compounds represented by formula (I) above, further more preferred are the N-methylol compounds represented by formula (Ia) above, and most preferred are the 1H-1,2,4-triazole-1-methanol compounds (i.e., Za of formula (Ia) is a nitrogen atom).
Preferred in the present invention are the N-methylol compounds having a pKa of an amine compound which is formed together with formaldehyde when dissolved in water being 8 or less, preferably 7 or less, more preferably 6 or less in water at a room temperature. The lower limit is 0.01 or more, preferably 0.1 or more, more preferably 0-5 or more, and most preferably 1 or more.
The N-methylol compound of the present invention is a water-soluble N-methylol compound, and has a total number of carbon atoms of preferably 15 or less, more preferably 12 or less, further more preferably 10 or less, and most preferably 6 or less.
Examples of the N-methylol compounds of the present invention are shown below, but are not limited thereto:
______________________________________ ##STR7##Com-pound R.sub.1 R.sub.2 R.sub.3______________________________________(I-1) H H H(I-2) CH.sub.3 H H(I-3) H CH.sub.3 H(I-4) H H CH.sub.3(I-5) CH.sub.3 H CH.sub.3(I-6) H H C.sub.2 H.sub.5(I-7) H H CH.sub.2 OH(I-8) H H CH.sub.2 OCH.sub.3(I-9) H H C.sub.3 H.sub.5 (n)(I-10) H H ##STR8##(I-11) H H ##STR9##(I-12) H C.sub.2 H.sub.5 H(I-13) H CH.sub.2 OH H(I-14) CH.sub.3 CH.sub.3 CH.sub.3(I-15) CH.sub.2 OH H CH.sub.3(I-16) CH.sub.3 H ##STR10##(I-17) ##STR11## CH.sub.2 OH(I-18) H H ##STR12##(I-19) H ##STR13## H(I-20) H H CO.sub.2 CH.sub.3(I-21) CH.sub.3 Cl CH.sub.3(I-22) H NO.sub.2 H(I-23) H H COCH.sub.3(I-24) OCH.sub.3 H CH.sub.3(I-25) CHCHCHCH H(I-26) H Cl H(I-27) H CO.sub.2 C.sub.2 H.sub.5 H(I-28) H CN H(I-29) CH.sub.3 H NHCOCH.sub.3(I-30) H NHCONHCH.sub.2 CH.sub.2 OH H(I-31) H H NHCO.sub.2 CH.sub.3(I-32) H H NHSO.sub.2 CH.sub.3______________________________________ ##STR14##
The N-methylol compounds of the present invention can be readily synthesized by reacting an amine compound such as pyrazole, 1,2,4-triazole or the derivative thereof with formaldehyde or praraformaldehyde. These syntheses can be carried out according to the methods described in U.S. Pat. No. 2,883,392, Chem. Ber., 85, 820 ('52), J. Org. Chem., 15,1285 ('50), European Patent 60,222A, and Khim. Geterotsikl. Soedin., (2), 251 ('80)[Chemical Abstracts, 93: 46530W]. Meanwhile, the pyrazole derivative can be synthesized by the methods described in R. H. Wiley "Pyrazoles, pyrazolines, Pyrazolidines, Indoles and Condensed Ring" in The Chemistry of Heterocyclic Compounds, Vol. 22, published by Interscience Publishers ('67), or by the methods corresponding thereto.
Syntheses examples of the N-methylol compounds of the present invention are shown below.
Synthesis 1--Compound (I-1)
Pyrazole (68.1 g), sodium hydrozide (0.14 g) and methanol (80 ml) were put in a 500 ml three-neck flask equipped with a stirrer, a thermometer and a condenser. After the temperature was raised to 50.degree. C., 90% paraformaldehyde (33 g) was added little by little and the stirring was applied at the same temperature for one hour. After reaction had finished, the solution was filtered and the filtrate was concentrated at a reduced pressure at 40.degree. C. or lower. Ethyl acetate (300 ml) was added to the concentrate thus obtained for crystallization, whereby Compound (I-1) of colorless crystal was obtained. (Yield: 72 g, melting point: 79.degree. to 84.degree. C.). The chemical structure thereof was confirmed with an elementary analysis and various spectra.
The equilibrium constant K of this compound was 5.6.times.10.sup.-3 mole/liter, wherein the equilibrium constant was obtained by measuring the heavy water solution of 25 millimole/liter of this compound with a nuclear magnetic resonance absorption method (NMR) and calculating from a portion ratio at the moment the components generated in the solution when the peak variation of NMR was not observed.
Further, the formaldehyde-releasing rate constant kr was 8.7.times.10.sup.-2 sec.sup.-1, wherein the constant kr was obtained in the following manner: formaldehyde and pyrazole were added to water at a room temperature and the amounts of this compound, formaldehyde and pyrazole were observed over time until they reached the equilibrium to obtain the generation speed constant kf of this compound; and the constant kf thus obtained was multiplied by the above equilibrium constant K to calculate the formaldehyde-releasing rate constant kr. This compound was detected by an ultraviolet spectroscopic method.
The pKa value of pyrazole generated by releasing from this compound was 2.5 in water at a room temperature.
Synthesis 2--Compound (I-5)
3,5-dimethylpyrazole (48.1 g), sodium hydroxide (0.07 g) and methanol (50 ml) were put in a 300 ml three-necks flask equipped with a stirrer, a thermometer and a condenser. After the temperature was raised to 50.degree. C., 90% paraformaldehyde (16.5 g) was added little by little and stirring was applied at the same temperature for one hour. After the reaction finished, the solution was filtered and the filtrate was concentrated at a reduced pressure at 40.degree. C. or lower. Ethyl acetate (150 ml) was added to the concentrate thus obtained for crystallization, whereby Compound (I-5) of a colorless crystal was obtained. (Yield: 28 g, melting point: 108.degree. to 111.degree. C.). The chemical structure thereof was confirmed with an elementary analysis and various spectra.
The equilibrium constant K of this compound was 3.3.times.10.sup.-3 mole/liter and the pKa of 3,5-dimethylpyrazole generated by releasing from this compound was 4.1 in water at a room temperature.
The equilibrium constants, K of typical N-methylol compounds of the present invention which are obtained according to the method of compound (I-1) and the comparative compounds are shown in Table 3 below.
TABLE 3______________________________________ Equilibrium Constant, KCompound No. (mol/liter) Remarks______________________________________I-1 5.6 .times. 10.sup.-3 InventionI-2 3.0 .times. 10.sup.-3 InventionI-3 2.7 .times. 10.sup.-3 InventionI-4 3.0 .times. 10.sup.-3 InventionI-6 3.3 .times. 10.sup.-3 InventionI-26 4.7 .times. 10.sup.-3 InventionI-27 7.5 .times. 10.sup.-3 InventionI-28 1.45 .times. 10.sup.-2 InventionI-29 6.5 .times. 10.sup.-3 InventionII-1 1.2 .times. 10.sup.-2 InventionII-2 1.4 .times. 10.sup.-3 or less InventionII-3 1.1 .times. 10.sup.-2 InventionComp. Compound (a) 1.3 .times. 10.sup.-3 ComparisonComp. Compound (b) 3.9 .times. 10.sup.-3 ComparisonComp. Compound (c) 1.2 .times. 10.sup.-1 ComparisonComp. Compound (d) 3.0 .times. 10.sup.-2 ComparisonComp. Compound (e) 3.6 .times. 10.sup.-1 ComparisonComp. Compound (f) 3.0 .times. 10.sup.-2 ComparisonComp. Compound (g) 9.3 .times. 10.sup.-2 ComparisonComp. Compound (h) 2.8 .times. 10.sup.-2 Comparison______________________________________
In Table 3, the comparative compounds (a) to (h) are shown below. ##STR15##
Further, of the compounds shown in Table 3, the formaldehyde-releasing rate constants, kr of the compounds (I-1), (II-2) and (II-3) and the comparative compounds (a), (b), (f) and (h) are shown in Table 4 below.
TABLE 4______________________________________ Formaldehyde-releasing rate constant, krCompound No. (sec.sup.-1) Remarks______________________________________ I-1 8.7 .times. 10.sup.-3 InventionII-2 2.0 .times. 10.sup.-3 InventionII-3 1.4 .times. 10.sup.-3 InventionComp. Compound (a) 4.5 .times. 10.sup.-3 ComparisonComp. Compound (b) 8.0 .times. 10.sup.-3 ComparisonComp. Compound (f) 9.9 .times. 10.sup.-3 ComparisonComp. Compound (h) 2.5 .times. 10.sup.-3 Comparison______________________________________
As is apparent from Table 3 and Table 4, the equilibrium constants of N-methylol products of pyrrole, imidazole or tetrazole compounds are more than 2.times.10.sup.-2 mol/liter and are out of the specific value of the present invention. Further, the equilibrium constants of N-methylol products of alicyclic amide compound or urea compound satisfy the specific value of the present invention, but the formaldehyde-releasing rate constants are small and are out of the specific value of the present invention.
The isolated N-methylol compounds of the present invention may be used as shown in the above synthetic examples, or the solution containing the N-methylol compounds of the present invention may be used as it is without isolating them in the above synthetic examples, wherein the solution is prepared by adding each equimolar amount of formaldehyde or paraformaldehyde and an amine compound such as pyrazole, 1,2,4-triazole, or the derivative thereof. Further, the N-methylol compound of the present invention may be contained in a processing bath, wherein formaldehyde or paraformaldehyde and an amine compound such as pyrazole, 1,2,4-triazole, or the derivative thereof are added to the processing bath to prepare the compound therein.
In the present invention, the color image-stabilization processing solution is defined as a solution having the effect of stabilizing the color image formed by a color development (particularly, the effect of preventing a fading of a magenta dye in storage), including their replenishing solutions. Accordingly, there are included therein the processing solutions used after the color development including their replenishing solutions. To be concrete, the processing solutions of the present invention include a stabilizing solution, a conditioning solution, a bleaching solution, a bleach-fixing solution and a stopping solution including the respective replenishing solutions. Preferably, the present invention is a stabilizing solution, a conditioning solution and a bleaching solution including their respective replenishing solutions, and particularly preferably a stabilizing solution including the replenishing solution thereof. In the present invention, a replenishing solution for a processing solution is defined as the solution which is used to replenish the components of the processing solution in a continuous processing.
The preferred embodiments are listed below:
(1) a stabilizing solution containing at least one N-methylol compound of the present invention,
(2) a stabilizing replenishing solution containing at least one N-methylol compound of the present invention,
(3) a conditioning solution containing at least one N-methylol compound of the present invention,
(4) a bleaching solution containing at least one N-methylol compound of the present invention,
(5) a method for processing with a stabilizing solution containing at least one N-methylol compound of the present invention,
(6) a method for processing while replenishing with a replenishing stabilizing solution containing at least one N-methylol compound of the present invention,
(7) a method for processing with a conditioning solution containing at least one N-methylol compound of the present invention, and
(8) a method for processing with a bleaching solution containing at least one N-methylol compound of the present invention.
Of these preferred embodiments, (1), (2), (5) and (6) are particularly preferred.
In the present invention, the stabilizing solution is defined as a stabilizing solution or washing-alternative stabilizing solution conventionally used at the final processing step of a color negative film and a color reversal film. When the final step comprises a washing step and a rinsing step, the stabilizing solution used at a stabilizing step prior thereto is included therein. It is used preferably at the final step.
The stabilizing solution and stabilizing replenishing solution conventionally used at the final step are the solutions containing formaldehyde as mentioned above and this formaldehyde has the effect of stabilizing an image.
In the present invention, formaldehyde is replaced with the N-methylol compound of the present invention to control the vapor pressure of formaldehyde at a lower level and stabilize the image. Accordingly, the color image-stabilization processing solution contains substantially no formaldehyde, wherein "contains substantially no formaldehyde" means that formaldehyde may be contained to such extent that the effects of the present invention can be attained. To be concrete, it means that the total content of formaldehyde and the hydrate thereof is 0.005 mole/liter or less. The lower the total content of formaldehyde and the hydrate thereof, the more preferable to lower the vapor pressure of formaldehyde, and it is particularly preferably 0.003 mole/liter or less.
The replenishing solutions for the respective processing solutions used in the present invention have the function of maintaining the properties of the processing solutions at the prescribed levels by replenishing the components which have decreased due to deterioration while processing and storing in an automatic processing machine and by conditioning the concentrations of the components eluted from the light-sensitive material in processing. Accordingly, the concentrations of the consumed components are higher in the replenishing solution than in the processing solution and those of the latter light-sensitive material components are lower in the replenishing solution than in the processing solution. The components which are less susceptible to variation of the concentration by processing and storing are contained usually in almost the same concentrations as those of the processing solutions.
The addition of the N-methylol compound of the present invention is preferably 0.003 to 0.1 mole, more preferably 0.005 to 0.03 mole per liter of the color image-stabilization processing solution.
The color image-stabilization processing solution to which the N-methylol compound of the present invention can be added and the other processing solutions which are used in the processing with the color image-stabilization processing solution of the present invention are described below. When the N-methylol compound of the present invention is used in processing solutions other than the stabilizing solution, the stabilizing solution may not contain the N-methylol compound of the present invention- In that case, the naming of the stabilizing solution is inappropriate because the processing solution itself no longer has the effect of stabilizing the color image, but hereafter it will be called that for convenience. Further, when the N-methylol compound of the present invention is added to a bleaching solution, a conditioning solution, etc., the naming of the bleaching solution, the conditioning solution, etc., are also inappropriate because these solutions have the stabilizing effect, but hereafter they will be called those respectively for convenience.
Described below are the stabilizing solution preferably containing the N-methylol compound of the present invention and the conditioning solution, which are used at the final step. The conditioning solution is processing solution which may be called the bleach-accelerating solution.
The stabilizing solution used at the final step can contain all compounds which can be added to washing water mentioned later. In particular, preferably contained therein are various surfactants for preventing irregularity by waterdrop in drying a light-sensitive material, various bactericides, anti-mold agents, fungicides and chelating agents for preventing generation of fur and mold grown on the light-sensitive material after processing. Further, there may be added an amine compound such as pyrazole, 1,2,4-triazole or the derivative thereof which contains no methylol group.
Also, in addition to the N-methylol compound of the present invention, the stabilizing solution may contain the compounds for stabilizing a dye image, for example, hexamethylenetetramine, a hexamethylenetetramine derivative, hexahydrotriazine, a hexahydrotriazine derivative, dimethylol urea, an organic acid, and a pH buffer agent. In addition to the above compounds, there can be used ammonium compounds such as ammonium chloride and ammonium sulfite, metal compounds containing Bi and Al, a fluorescent whitening agent, a hardener, and alkanol-amines described in U.S. Pat. No. 4,786,583.
The stabilizing solution used at the final step is used usually at pH ranging from 4 to 9, preferably 6 to 8.
Where the stabilizing solution of the present invention is used at the final step, the replenishing amount thereof is preferably 200 to 1500 ml, more preferably 300 to 600 ml, per m.sup.2 of the light-sensitive material.
Where the stabilizing solution of the present invention is used at the final step, the processing temperature is preferably 30.degree. to 45.degree. C.; the processing time is preferably 10 seconds to 2 minute, particularly 15 to 30 seconds.
In addition to the N-methylol compound of the present invention, there can be incorporated into the conditioning bath, aminocarboxylic acid chelating agents such as ethylenediaminetetraacetic acid, diethylentriaminepentaacetic acid, 1, 3-diaminopropanetetraacetic acid, and cyclohexanediaminetetraacetic acid; and various bleach-accelerating agents including sulfites such as sodium sulfite and ammonium sulfite, thioglycerine, aminoethanethiol, and sulfoethanethiol.
Further, for the purpose of preventing scums there are preferably incorporated therein sorbitan esters of fatty acids substituted with ethylene oxide, described in U.S. Pat. No. 4,839,262, and polyoxyethylene compounds described in U.S. Pat. No. 4,059,446 and Research Disclosure., vol.191, 19104 (1980).
These compounds can be used in the range of 0.1 to 20 g, preferably 1 to 5 g, per liter of the conditioning solution.
The pH value of the conditioning solution is usually 3 to 11, preferably 4 to 9, and more preferably 4 . 5 to 7.
The processing time in the conditioning solution is 30 seconds to 5 minutes.
The replenishing amount for the conditioning solution is preferably 30 to 3000 ml, particularly preferably 50 to 1500 ml, per m.sup.2 of a light-sensitive material.
The processing temperature of the conditioning solution is preferably 20.degree. to 50.degree. C., particularly preferably 30.degree. to 40.degree. C.
Usually, after being subjected it to an imagewise exposure, a silver halide color photographic light-sensitive material is subjected to a color development in the case of negative type and positive type light-sensitive materials, and to a color development following a black/white development and a reversal processing in the case of a reversal positive type light-sensitive material.
The color developing solution which can be used in the present invention is an alkaline aqueous solution containing an aromatic primary amine color developing agent as the main component.
The preferred color developing agent is a p-phenylenediamine derivative. Representative examples thereof are shown below, but are not limited thereto:
D-1 N,N-diethyl-p-phenylenediamine;
D-2 2-Methyl-N,N-diethyl-p-phenylenediamine;
D-3 4-[N-ethyl-N-(.beta.-hydroxyethyl) amino] aniline;
D-4 2-Methyl-4-[N-ethyl-N-(.beta.-hydroxyethyl) amino] aniline;
D-5 4-Amino-3-methyl-N-[.beta.-(methanesulfonamide) ethyl aniline;
D-6 4-Amino-3-methyl-N-ethyl-N-methoxyethylaniline; and
D-7 4-Amino-3-methyl-N-ethyl-N-(4-hydroxybutyl) aniline.
Among the above p-phenylenediamine derivatives, D-4 and D-5 are preferred.
These p-phenylenediamine derivatives may be sulfates, chlorates, sulfites and p-toluenesulfonates thereof.
The aromatic primary amine color developing agent is used preferably in a concentration of 0.001 to 0.1 mole, more preferably 0.01 to 0.06 mole, per liter of the color developing solution.
There can be added as a preservative to the color developing solution, sodium sulfite, potassium sulfite, sodium bisulfite, potassium bisulfite, sodium metasulfite, potassium metasulfite, and a carbonyl sulphurous acid adduct, according to necessity.
The addition amount of these preservatives is preferably 0.5 to 10 g, more preferably 1 to 5 g, per liter of the color developing solution.
Examples of the compounds for preserving directly the above aromatic primary a3nine color developing agent include the various hydroxylamines described in JP-A-63-5341 and JP-A-63-106655 (above all, preferred are the compounds having a sulfo group and a carboxy group); the hydroxamic acids described in JP-A-63-43138; the hydrazines and hydrazides described in JP-A-63-146041; the phenols described in JP-A-63-44657 and JP-A-63-58443; the .alpha.-hydroxy ketones and .alpha.-aminoketones described in JP-A-63-44656; and the various kinds of sucrose described in JP-A-63-36244.
Also, there can be used in combination with the above compounds: monoamines described in JP-A-63-4235, JP-A--63-24254, JP-A-63-21647, JP-A-63-146040, JP-A-63-27841, and JP-A-63-25654; diamines described in JP-A-63-30845, JP-A-63-14640, and JP-A-63-43139; polyamines described in JP-A-63-21647, JP-A-63-26655, and JP-A-63-44655; nitroxy radicals described in JP-A-63-53551; alcohols described in JP-A-63-43140 and JP-A-63-53549; oximes described in JP-A-63-56654;and tertiary amines described in JP-A-63-239447.
There may be contained according to necessity the other preservatives such as the various metals described in JP-A-57-44148 and JP-A-57-53749; the salicylic acids described in JP-A-59-180588; the alkanolamines described in JP-A-54-3582; the polyethyleneimines described in JP-A-56-94349; and the aromatic polyhydroxy compounds described in U.S. Pat. No. 3,746,544. Among them, the aromatic polyhydroxy compounds are particularly preferable.
The color developing solution preferably has pH of 9 to 12, more preferably 9 to 11.0.
In order to maintain a pH at the above level, various buffer agents are preferably used.
Examples of the buffer agent 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, sodium o-hydroxybenzoate (sodium salicylate, potassium o-hydroxybenzoate, sodium 5-sulfo-2-hydroxybenzoate (sodium 5-sulfosalicylate), and potassium 5-sulfo-2-hydroxybenzoate (potassium 5-sulfo-salicylate). The addition amount of the buffer agent is preferably 0.1 mole or more, more preferably 0.1 to 0.4 mole, per liter of the color developing solution.
In addition to the above compounds, various chelating agents are preferably used as an anti-precipitation agent for calcium and magnesium or for the purpose of improving the stability of the color developing solution. Organic acid compounds are preferred as the chelating agent and examples thereof include amino-polycarboxylic acids, organic phosphonic acids and phosphonocarboxylic acids.
Representative examples thereof are di-ethylenetriaminepentaacetic acid, ethylenediaminetetraacetic acid, N,N,N-trimethylenephosphonic acid, ethylenediamine N,N,N',N'-tetramethylenephosphonic acid, transcyclohexanediaminetetraacetic acid, 1,2-diamino-propanetetraacetic acid, hydroxyethyliminodiacetic acid, glycol ether diaminetetraacetic acid, ethylenediamine-orthohydroxyphenylacetic acid, phosphonobutane-1,2,4-tricaboxylic acid, 1-hydroxyethylidene-1,1-diphosphonic acid, and N,N'-bis(2-hydroxybenzyl) ethylenediamine-N,N'-diacetic acid.
These chelating agents may be used in combination of two or more, according to necessity.
The addition amount of the chelating agent may be an amount sufficient to capture metal ions and is at a level, for example, of 0.1 to 10 g per liter of the color developing solution.
Arbitrary development accelerators can be added to the color developing solution according to necessity. However, the color developing solution used in the present invention preferably contains substantially no benzyl alcohol from the viewpoint of a public pollution, the preparing property of the solution and the prevention of a color stain. The term "substantially no benzyl alcohol" means that it is contained in the amount of 2 ml or less per liter of the color developing solution and preferably it is not contained at all.
There can be added as the other development accelerators, the thioether compounds described in JP-B-37-16088 (the term "JP-B" as used herein means an examined Japanese patent publication), JP-B-37-5987, JP-B-38-7826, JP-B-44-12380, and JP-B-45-9019, and U.S. Pat. No. 3,818,247; the p-phenylenediamine compounds described in JP-A-52-49829 and JP-A-50-15554; the quaternary ammonium salts described in JP-A-50-137726, JP-B-44-30074, JP-A-56-156826 and JP-A-52-43429; the amine compounds described in U.S. Pat. Nos. 2,494,903, 3,128,182, 4,230,796, 3,253,919, 2,482,546, 2,596,926, and 3,582,346, and JP-B-41-11431; the polyalkylene oxide described in JP-B-37-16088, JP-B-42-25201, JP-B-41-11431 and JP-B-42-23883, and U.S. Pat. Nos. 3,128,183 and 3,532,501; 1-phenyl-3-pyrazolidones; and imidazoles. They can be added according to necessity.
The addition amount of the development accelerator is 0.01 to 5 g per liter of the color developing solution.
In the present invention, an arbitrary anti-foggant can further be added according to necessity.
There can be used as the anti-foggant, an alkali metal halide such as sodium chloride, potassiumbromide and potassium iodide, and an organic anti-foggant. Typical examples of the organic anti-foggant are the nitrogen-containing heterocyclic compounds such as benzotriazole, 6-nitrobenzimidazole, 5-nitrosoindazole, 5-methylbenzotriazole, 5-nitrobenzotriazole, 5-chlorobenzotriazole, 2-thiazolyl-benzimidazole, 2-thiazolylmethyl-benzimidazole, indazole, hydroxyazaindolizine, and adenine. The addition amount of the anti-foggant is 0.01 to 1 g per liter of the color developing solution.
The color developing solution used in the present invention may contain a fluorescent whitening agent. The 4,4'-diamine-2,2'-disulfostilbene compounds are preferred as the fluorescent whitening agent. The addition amount thereof is 0 to 5 g, preferably 0.1 to 4 g, per liter of the color developing solution.
Also, there may be added various surfactants such as alkylsulfonic acid, arylsulfonic acid, aliphatic carboxylic acid, and aromatic carboxylic acid.
A color developing-replenishing solution contains the compounds contained in the color developing solution. The functions of the color developing-replenishing solution are (i) to replenish to the color developing solution, the compounds which are consumed due to processing of a light-sensitive material and deterioration caused during the storage in an automatic developing machine and (ii) to maintain the developing properties at the fixed levels by conditioning the concentrations of the compounds eluted from the light-sensitive material by processing. Accordingly, the concentrations of the former are maintained higher than those of the color developing tank solution, and those of the latter are lower. Examples of the former compounds are the color developing agent and preservative, which are contained in amounts 1.1 to 2 times as large as those of the tank solution in the replenishing solution. An example of the latter compound is a development inhibitor represented by halide (for example, potassium bromide), and it is contained in the replenishing solution in the amount 0 to 0.6 times that of the tank solution.
The concentration of the halides in the replenishing solution is usually 0.006 mole/liter or less and has to be decreased more in a lower replenishing, or it may not be contained at all.
The compounds which are less susceptible to concentration variation resulting from processing and storing are contained in the same concentrations as those of the color developing tank solutions. The examples thereof are the chelating agent and the buffer agent.
Further, the pH of the color developing-replenishing solution is maintained higher by 0.05 to 0.5 than that of the tank solution. This difference of pH has to be increased according to the decrease in the replenishing amount.
The color developing solution is replenished in the amount of 3000 m or less, preferably 100 to 1500 ml, per m.sup.2 of the light-sensitive material.
The processing temperature in the color developing solution is suitably 20.degree. to 50.degree. C., preferably 30.degree. to 45.degree. C. The processing time is suitably 20 seconds to 5 minutes, preferably 30 seconds to 3 minutes and 20 seconds, and more preferably 1 minute to 2 minutes and 30 seconds.
Also, a color developing bath may be divided into two or more baths according to the need to replenish the color developing-replenishing solution from the front or rear bath thereby to shorten the processing time and reduce the replenishing amount.
The processing method of the present invention can be preferably applied to color reversal processing. Reversal processing is carried out according necessity and then the color development is performed. A black/white developing solution used for the above processing is a so-called first black/white developing solution used for reversal processing of a conventional color light-sensitive material. It can contain various well-known additives which are added to a black/white developing solution used for processing a black/white silver halide light-sensitive material.
Representative additives include developing agents such as 1-phenyl-3-pyazolidone, Metol and hydroquinone, a preservative such as sulfite, an accelerator consisting of an alkali such as sodium hydroxide, sodium carbonate and potassium carbonate, an inorganic or organic inhibitor such as potassium bromide, 2-methylbenzimidazole and methylbenzthiazole, a hard water softener such as polyphosphoric acid, and a development inhibitor consisting of a trace amount of iodide and a mercapto compound.
When processing is carried out with the above black/white developing solution or color developing solution in an automatic developing machine, the area (opening area) in which the developing solution (the color developing solution and black/white developing solution) contacts air is preferably as small as possible. For example, the opening ratio is preferably 0.01 cm.sup.-1 or less, more preferably 0.005 cm.sup.-1 or less, wherein the opening ratio is obtained by dividing an opening area (cm.sup.2) by the volume (cm.sup.3) of the developing solution.
The developing solution can be regenerated for reuse. The regeneration of the developing solution means that the used developing solution is subjected to treatment with an anionic exchange resin and an electro-dialysis, or the processing chemicals called as the regenerating agents are added to the used developing solution, to increase the activity of the developing solution and use it once again as the processing solution.
A regeneration rate (the rate of an overflow solution in a replenishing solution) is preferably 50% or more, particularly 70% or more.
In the processing in which the regeneration of the developing solution is used, the overflow solution is used as the replenishing solution after regenerating.
In a regeneration method, an anionic exchange resin is preferably used. The particularly preferred composition of the anionic exchange resins and the regeneration method of the resins are described in Diaion Manual (I) (14th edition, 1986) published by Mitsubishi Chemical Industry Co., Ltd. Of the anionic exchange resin reins, the resins of the composition described in JP-A-2-952 and JP-A-1-281152 are preferred.
In the present invention, the light-sensitive material after being subjected to color development is subjected to a desilvering processing. The desilvering processing as described herein consists basically of a bleaching processing and a fixing processing. Usually, it consists of a bleach-fixing processing in which both are simultaneously carried out, and the combination of these processings.
The representative desilvering processing steps are shown below:
1. Bleaching--fixing
2. Bleaching--bleach-fixing
3. Bleaching--washing--fixing
4. Bleaching--bleach-fixing--fixing
5. Bleach-fixing
6. Fixing--bleach-fixing
Of the above steps, the steps 1, 2, 4 and 5 are particularly preferred. The step 2 is disclosed in, for example, JP-A-61-75352. The step 4 is disclosed in JP-A-61-143755 and Japanese Patent Application No. 2-216389.
The baths such as the bleaching bath and fixing bath applied to the above steps may be a one bath structure or a two or more bath structure (for example, 2 to 4 baths, wherein a counter-current replenishing system is preferable).
The above desilvering processing step may be carried out following a rinsing, washing and stopping after color developing. In the processing of a negative light-sensitive material, it is preferably carried out immediately after color developing, and in a reversal processing it is preferably carried out following a conditioning bath after color developing.
The bleaching solution can contain an N-methylol compound of the present invention. There can be mentioned as the bleaching agent contained as the main component for the bleaching solution of the present invention, inorganic compounds such as red prussiate, ferric chloride, bichromates, persulfates, and bromates, and semi-organic compounds such as an aminopolycarboxylic acid ferric complex salt and an aminopolyphosphonic acid ferric complex salt.
In the present invention, an aminopolycarboxylic acid ferric complex salt is preferably used from the viewpoint of environmental preservation, safety in handling and corrosion to metal.
Examples of the ferric complex salt of aminopolycarboxylic acid are shown below together with an oxidation/reduction potential, but these complexes are not limited thereto:
______________________________________Compound No. Potential*______________________________________1. Ferric complex salt of N-(2-acetamide) 180 iminodiacetic acid2. Ferric complex salt of methyliminodiacetic 200 acid3. Ferric complex salt of iminodiacetic acid 2104. Ferric complex salt of 2,4-butylenediamine- 230 tetraacetic acid5. Ferric complex salt of diethylenethioether- 230 diaminetetraacetic acid6. Ferric complex salt of glycol ethr diamine- 240 tetraacetic acid7. Ferric complex salt of 1,3-propylenediamine- 250 tetraacetic acid8. Ferric complex salt of ethylenediamine- 110 tetraacetic acid9. Ferric complex salt of diethylenetriamine- 80 pentacetic acid 10. Ferric complex salt of trans-1,2-cyclohexane- 80 diaminetetraacetic acid______________________________________ *Oxidation/reduction potential (mV vs. NHE, pH = 6)
The oxidation/reduction potential of the above bleaching agents is defined by the oxidation/reduction potential obtained by measuring with the method described in Transactions of the Faraday Society, vol. 55 (1959), pp. 1312 to 1313.
In the present invention, from the viewpoint of rapid processing and effective demonstration of the effects of the present invention, the bleaching agent has preferably an oxidation/reduction potential of 150 mV or more, more preferably 180 mV or more, and most preferably 200 mV or more. The bleaching agent having too high an oxidation/reduction potential causes bleaching fog and therefore, the upper limit thereof is 700 mV or less, preferably 500 mV or less.
Of the above compounds, particularly preferred is Compound No. 7, the ferric complex salt of 1,3-propylenediaminetetraacetic acid.
The ferric complex salt of aminopolycarboxylic acid is used in the form of sodium, potassium and ammonium salts. Of them, the ammonium salt is preferred in terms of the most rapid bleaching speed.
The amount of the bleaching agent used in the bleaching solution is preferably 0.17 to 0.7 mole, more preferably 0.25 to 0.7 mole in terms of a rapid processing and reduction of stain by aging and particularly preferably 0.30 to 0.6 mole, per liter of the bleaching solution. Further, the amount of the bleaching agent used in the bleach-fixing solution is 0.01 to 0.5 mole, more preferably 0.02 to 0.2 mole, per liter of the bleach-fixing solution.
In the present invention, the bleaching agent may be used singly or in a combination of two or more. Where two or more bleaching agents are used, the total amount thereof may fall within the above range.
When the ferric complex salt of aminopoly-carboxylic acid is used in the bleaching solution, it can be added in the form of a complex salt as mentioned above, or aminopolycarboxylic acid which is a complex-forming compound and a ferric salt (for example, ferric sulfate, ferric chloride, ferric nitrate, ferric ammonium sulfate and ferric phosphate) may coexist to form the complex salt thereof.
Where the complex salt is formed in the above manner, the aminopolycarboxylic acid may be added in a little more excessive amount than that necessary for forming the complex salt with a ferric ion, wherein it is used preferably in excess of 0.01 to 10%.
In general, the above bleaching solution is used at pH of 2 to 7.0. For rapid processing, the pH of the bleaching solution is preferably 2.5 to 5.0, more preferably 3.0 to 4.8, particularly preferably 3.5 to 4.5. That of the replenishing solution is 2.0 to 4.2.
In the present invention, conventional acids can be used to control pH in the above ranges. The acids used therefor have preferably pKa of 2 to 5.5, wherein pKa is defined by the cologarithm of a dissociation constant of acid and is the value obtained in the conditions of an ionic strength of 0.1 mole/dm and 25.degree. C.
Acids having pKa ranging from 2.0 to 5.5 are preferably incorporated into the bleaching solution in an amount of 0.5 mole/liter or more since bleaching fog and precipitation in the replenishing solution in storing at a lower temperature occur.
The acids having pKa ranging from 2.0 to 5.5 may be inorganic acids such as phosphoric acid and organic acids such as acetic acid, malonic acid and citric acid. The acids showing the above improvement are the organic acids. Among such organic acids, particularly preferred are the organic acids having a carboxyl group.
The organic acids having pKa of 2.0 to 5.5 may be a monobasic acid or a polybasic acid. Where they are polybasic acids, they can be used in the form of metal salts (for example, sodium ad potassium salts) and ammonium salts as long as the pKa values thereof range from 2.0 to 5.5.
The organic acids having a pKa of 2.0 to 5.5 may be used in combination of two or more, provided that aminopolycarboxylic acid, the salt thereof and the Fe complex salt thereof are excluded from the acids as described herein.
The preferred examples of organic acids having a pKa of 2.0 to 5.5 are aliphatic monobasic acids such as acetic acid, monochloroacetic acid, monobromoacetic acid, glycolic acid, propionic acid, monocloropropionic acid, lactic acid, pyruvic acid, acrylic acid, butyric acid, isobutyric acid, pivaric acid, aminobutyric acid, valetic acid, and isovaleric acid; amino acid compounds such as asparagine, alanine, arginine, ethionine, glycine, glutamine, cysteine, serine, methionine, and leucine; aromatic monobasic acids such as benzoic acid, monosubstituted (for example, chloro and hydroxy) benzoic acid, and nicotinic acid; aliphatic dibasic acids such as oxalic acid, malonic acid, succinic acid, tartaric acid, malic acid, maleic acid, fumaric acid, oxaloacetic acid, glutaric acid, and adipic acid; dibasic amino acids such as aspattic acid, glutamic acid, and cystine; aromatic dibasic acids such as phthalic acids and terephthalic acid; and polybasic acids such as citric acid.
Among them, the monobasic acids having a hydroxyl group and a carboxyl group are preferred and particularly preferred are glycolic acid and lactic acid.
Glycolic acid and lactic acid are used in an amount of 0.2 to 2 mole, preferably 0.5 to 1.5 mole per liter of the bleaching solution. These acids are preferred since they can more notably demonstrate the effects of the present invention while they generate no odor and inhibit bleaching fog.
Also, the combined use of acetic acid and glycolic acid or lactic acid is preferred since it can markedly provide the effects of solving either of the problems of precipitation and bleaching fog. The molar ratio of acetic acid to glycolic acid or lactic acid used in combination is preferably 1:2 to 2:1.
The total amount of these acids used is suitably 0.5 mole or more, preferably 1.2 to 2.5 mole, and more preferably 1.5 to 2.0 mole, per liter of the bleaching solution.
When the pH of the bleaching solution is controlled in the above-described range, there may be used the above acids and alkali agents (for example, ammonia water, KOH, NaOH, imidazole, monoethanolamine, and diethanolamine). Among them, ammonia water is preferred.
Also, potassium carbonate, ammonia water, imidazole, monoethanolamine or diethanolamine is preferably used as an alkali agent for a bleaching starter used in preparing a starting solution of a bleaching solution from a replenishing solution. The diluted replenishing solution itself may be used without using the bleaching starter.
In the present invention, various bleaching accelerators can be added to the bleaching bath and the prebaths thereof. For example, there can be used the compounds having a mercapto group or a disulfide group, described in U.S. Pat. No. 3,893,858, German Patent 1,290,821, British Patent 1,138,842, JP-A-53-95630, and Research Disclosure, Vol. 17129 (July 1978); the thiazolidine derivatives described in JP-A-50-140129; the thio-urea derivatives described in U.S. Pat. No. 3,706,561; the iodides described in JP-A-58-16235; the polyethylene oxides described in German Patent 2,748,430; and the polyamine compounds described in JP-B-45-8836. Among the above compounds, particularly preferred are the mercapto compounds described in British Patent 1,138,842 and JP-A-2-190856.
The bleaching solution used in the present invention can contain the rehalogenization agents such as bromides (for example, potassium bromide, sodium bromide and ammonium bromide) and chlorides (for example, potassium chloride, sodium chloride and ammonium chloride). The concentration of the rehalogenization agent is 0.1 to 5.0 mole, preferably 0.5 to 3.0 mole, per liter of the processing solution.
Further, ammonium nitrate is preferably used as an anti-corrosion agent to protect metal.
In the present invention, a replenishing system is preferably applied. The bleaching solution is replenished preferably in amount of 600 ml or less, more preferably 100 to 500 ml, per m.sup.2 of the light-sensitive material.
The bleaching time is 120 seconds or shorter, preferably 50 seconds or shorter and more preferably 40 seconds or shorter.
In processing, the bleaching solution containing the ferric complex salt of an aminopolycarboxylic acid is subjected to aeration to oxidize the formed ferric complex salt of aminopolycarboxylic acid, whereby the oxidizing agent is regenerated and the photographic properties are quite stably maintained.
In processing with the bleaching solution in the present invention, particularly the bleaching solution containing a high-potential bleaching agent, a so-called evaporation correction is preferably carried out, in which water corresponding to the evaporated processing solution is supplied.
The concrete methods of replenishing water in such a way are not specifically limited. Preferred among them are the methods described in JP-A-1-254959 and JP-A-1-254960, in which the amount of water evaporated from a monitoring bath settled separately from the bleaching bath is measured and the amount of water evaporated from the bleaching bath are calculated from the above amount of water to replenish the amount of water proportional thereto to the bleaching bath; and the evaporation-correction methods are described in Japanese Patent Application Nos. 2-46743, 2-47777, 2-47778, 2-47779, and 2-117972, in which a solution level sensor and an overflow sensor are used.
In the present invention, a light-sensitive material is processed with a processing solution having a fixing ability after processing with the bleaching solution. To be concrete, the processing solution having the fixing ability as described herein is a fixing solution and a bleach-fixing solution. Where the processing having a bleaching ability is carried out in the bleach-fixing solution, it may be combined with the processing having a fixing ability as shown in the above step 5. In the above steps 2 and 4 in which the processing with the bleach-fixing solution is carried out after the bleaching processing with the bleaching solution, the different bleaching agents may be contained in the bleaching solution and bleach-fixing solution, respectively. Where a washing step is interposed between the bleaching and fixing steps, the N-methylol compound of the present invention may be contained as well in the processing solutions used in those steps.
A fixing agent is contained in the processing solution having the fixing ability. The fixing agent may be thiosulfates such as sodium thiosulfate, ammonium thiosulfate, ammonium sodium thiosulfate, and potassium thiosulfate; thiocyanates (rhodanates) such as sodium thiocyanate, ammonium thiocyanate, and potassium thiocyanate; thioureas; and thioethers. Among them, ammonium thiosulfate is preferably used. The fixing agent is used in the amount of 0.3 to 3 mole, preferably 0.5 to 2 mole, per liter of the processing solution having the fixing ability.
Further, from the viewpoint of accelerating of the fixing, preferably used are above ammonium thiocyanate (ammonium rhodanate), thiourea and thioether (for example, 3,6-dithia-1,8-octanediol) in combination with thiosulfates. Of them, most preferably used are thiosulfate and thiocyanate in combination. The combined use of ammonium thiosulfate and ammonium thiocyanate is particularly preferred.
The amount of these compounds used in combination is 0.01 to 1 mole, preferably 0.1 to 0.5 mole per liter of the processing solution having fixing ability. On some occasions, the use of 1 to 3 mole can increase the fixing-acceleration effect to a large extent.
There can be incorporated into the processing solution having the fixing ability, preservatives such as sulfites (for example, sodium sulfite, potassium sulfite and ammonium sulfite), hydroxylamines, hydrazines, bisulfite adducts of aldehyde compounds (for example, acetaldehyde sodium bisulfite, particularly preferably the compounds described in Japanese Patent Application No. 1-298935), and the sulfinic acid compounds described in JP-A-1-231051.
Further, there can be incorporated therein various fluorescent whitening agents, defoaming agents, surfactants, polyvinylpyrrolidone, and organic solvents such as methanol.
The chelating agents such as aminopoly-carboxylic acids and organic phosphonic acids are preferably added to the processing solution having fixing ability. Preferred chelating agents include 1-hydroxyethylidene-1,1-diphosphonic acid, ethylenediamino-N,N,N',N'-tetramethylenephosphonic acid, nitrilotrimethylenephosphonic acid, ethylenediaminetetraacetic acid, diethyelentriaminepentaacetic acid, cyclohexanediaminetetraacetic acid, and 1,2-propylenediaminetetraacetic acid. Among them, particularly preferred are 1-hydroxyethylidene-1,1diphosphonic acid and ethylenediaminetetraacetic acid.
The addition amount of the chelating agent is 0.01 to 0.3 mole, preferably 0.1 to 0.2 mole, per liter of the processing solution.
The fixing solution has preferably a pH of 5 to 9, more preferably 7 to 8. The bleach-fixing solution has preferably a pH of 4.0 to 7.0, more preferably 5.0 to 6.5. Further, the bleach-fixing solution after processing with a bleaching solution or a first bleach-fixing bath has preferably a pH of 6 to 8.5, more preferably 6.5 to 8.
The processing solution having fixing ability preferably contains a compound having pKa ranging from 6.0 to 9.0 for the purpose of conditioning the pH thereof in the above range and as a buffer agent. The preferred examples of such compounds are imidazoles such as imidazole and 2-methylimidazole. The additional amount of these compound is 0.1 to 10 mole, preferably 0.2 to 3 mole, per liter of the processing solution.
The bleach-fixing solution can contain the foregoing compounds which can be contained in the bleaching solution.
In the present invention, the bleach-fixing solution (a start solution) in starting the processing is prepared by dissolving the foregoing compounds used for the bleach-fixing solution in water. It may be prepared by mixing suitable amounts of a bleaching solution and a fixing solution, each prepared separately.
The replenishing amount of the fixing solution or bleach-fixing solution in applying a replenishing system is preferably 100 to 3000 ml, more preferably 300 to 1800 ml, per m.sup.2 of the light-sensitive material.
The bleach-fixing replenishing solution itself may be replenished to the bleach-fixing solution, or the overflow solutions of the bleaching solution and the fixing solution may be used as the replenishing solution, as described in JP-A-61-143755 and Japanese Patent Application No. 2-216389.
Similar to the foregoing bleaching processing, bleach-fixing processing is preferably carried out while replenishing the water in an corresponding to the evaporated amount thereof, in addition to replenishing the processing solution.
In the present invention, the total processing time in the processing having a fixing ability is 0.5 to 4 minutes, preferably 0.5 to 2 minutes and particularly preferably 0.5 to 1 minute.
In the present invention, the total processing time in the desilvering processing comprising the combination of the bleaching, bleach-fixing and fixing steps is preferably 45 seconds to 4 minute, more preferably 1 to 2 minutes. The processing temperature is 25.degree. to 50.degree. C., preferably 35.degree. to 45.degree. C.
In the present invention, silver can be recovered from the used processing solution having fixing ability by conventional methods, and the regenerated solution after silver recovery can be reused. The effective silver recovering methods are an electrolysis method (described in French Paten 2,299,667), a setting method (described in JP-A-52-73037 and German Patent 2,331,220), an ion exchange resin method (described in JP-A-51-17114 and German Patent 2,548,237), and a metal substitution method (described in British Patent 1,353,805). These silver recovering methods are preferably carried out for the tank solutions in an inline system since the rapid processability can be further improved.
Usually, a washing processing step is performed after the processing step having the fixing ability.
There can be used a simple processing method in which a stabilizing processing is carried out with the stabilizing solution of the present invention without carrying out substantial washing after processing with the processing solution having fixing ability.
Washing water used in a washing step can contain various surfactants in order to prevent speckles by waterdrop on the light-sensitive material in drying after processing. The surfactant may be polyethylene glycol type nonionic surfactants, polyhydric alcohol type nonionic surfactants, alkylbenzenesulfonate type anionic surfactants, higher alcohol sulphuric ester salt type anionic surfactants, alkylnaphthalenesulfonate type anionic surfactants, quaternary ammonium salt type cationic surfactants, amine salt type cationic surfactants, amino salt type amphoteric surfactants, and betaine type amphoteric surfactants. Among them, the nonionic surfactants are preferably used. Particularly preferred are the alkylphenol-ethylene oxide adducts. Particularly preferred alkylphenols are octyl-, nonyl-, dodecyl- and dinonylphenols. The adduct molar number of ethylene oxide is particularly preferably 8 to 14. Further, silicone type surfactants having a higher defoaming effect are preferably used.
Various bactericides and fungicides may be added to the washing water in order to prevent the generation of fur and growth of mole on a light-sensitive material after processing. Examples of such bactericides and fungicides include thiazolylbenzimidazole type compounds described in JP-A-57-157244 and JP-A-58-105145; isothiazolone type compounds described in JP-A-57-8542; chlorophenol type compounds represented by trichlorophenol; bromophenol type compounds; organic tin and organic zinc compounds; acid amide compounds; diazine and triazine compounds; thiourea compounds; benzotriazole compounds; aklylguanidine compounds; quaternary ammonium compounds represented by benzoalcohonium chloride; antibiotics represented by penicillin; and conventional fungicides described in J. Antibact. Antifung. Agents, Vol. 1, No. 5, pp. 207 to 223 (1983). They may be used in combination of two or more. Also, the various fungicides described in JP-A-48-83820 can be used.
Further, various chelating agents are preferably contained in the washing water. The preferred chelating agents include aminopolycarboxylic acids such as ethylenediaminetetraacetic acid and diethylenetriaminepentaacetic acid, organic phosphonic acids such as 1-hydroxyethylidene-1,1-diphosphonic acid, ethylenediaminetetraacetic acid and diethylenetriamine-N,N,N',N'-tetramethylenephosphonic acid, and the hydrolysis products of maleic anhydride polymer described in EP 345172 Al.
The preservatives which can be contained in the above fixing solution and bleach-fixing solution are preferably contained in the washing water.
The washing step and stabilizing step are preferably in a multi-stage counter current system. The number of stages is preferably 2 to 4. The replenishing amount thereof is 1 to 50 times the amount carried over from the preceding bath, preferably 2 to 30 times, and more preferably 2 to 15 times, per unit area.
Tap water can be used for the washing step. Preferably used are water which has been subjected to a deionization treatment in which Ca and Mg ions are reduced to the concentration of 5 mg/liter or less with ion exchange resins, and water which has been sterilized with halogen or a ultraviolet sterilizing light.
Tap water may be used for correcting water evaporated from the respective processing solutions. Preferably used is deionized or sterilized water preferably used in the above washing step.
Further, an overflowing solution from the washing step or the stabilizing step is preferably flowed in the bath having a fixing ability which is the preceding bath since waste amount can be reduced.
In processing, a suitable amount of water, a correction solution or a replenishing solution is preferably added not only to the bleaching solution, bleach-fixing solution and fixing solution but also to the other processing solutions (for example, the color developing solution, washing water and stabilizing solution) in order to correct for the enrichment attributable to evaporation.
The effect of the present invention can be effectively demonstrated especially when the total processing time until the start of the drying step following the bleaching step is 1 to 3 minutes, preferably 1 minute and 20 seconds to 2 minutes.
In the present invention, the drying temperature is preferably 50.degree. to 65.degree. C., more preferably 50.degree. to 60.degree. C. The drying time is preferably 30 seconds to 2 minutes, more preferably 40 to 80 seconds.
The light-sensitive material used in the present invention may be provided on a support with at least one of the silver halide emulsion layers comprising a blue-sensitive layer, a green-sensitive layer and a red-sensitive layer, and there are specifically no limits to the number and order of the silver halide emulsion layers and light-insensitive layers.
One typical example is a silver halide color photographic light-sensitive material having on a support a light-sensitive layer comprising a plurality of the silver halide emulsion layers having substantially the same spectral sensitivities but different sensitivities, wherein the light-sensitive layer comprises a unit light-sensitive layer having spectral sensitivity to any of blue light, green light and red light. In a multi-layer silver halide color photographic light-sensitive material, the unit light-sensitive layers of a red-sensitivity, a green-sensitivity and a blue sensitivity are usually provided in order from the support side. According to purposes, however, the above order may be changed or a layer having a different spectral sensitivity can be interposed between the layers having the same spectral sensitivity.
Various light-insensitive layers such as an intermediate layer may be provided between the above silver halide light-sensitive layers and on the uppermost or lowermost layer.
The intermediate layer may contain the couplers described in JP-A-61-43748, JP-A-59-113438, JP-A-59-113440, JP-A-61-20037, and JP-A-61-20038 and further may contain an anti-color mixing agent, a ultraviolet absorber and an anti-stain agent, as usually used.
The plurality silver halide emulsion layers constituting the respective until light-sensitive layers can preferably have two layer structures consisting of a high-sensitive layer and low-sensitive layer, as described in German Patent 1,121,470 or British Patent 923,045. Usually, a lower-sensitive layer is provided more closely to the support. Also, a light-insensitive layer may be provided between the respective silver halide emulsion layers.
A lower-sensitive layer may be provided farther from the support and a high-sensitive layer more closely, as described in JP-A-57-112751, JP-A-62-200350, JP-A-62-206541, and JP-A-62-206543.
A concrete example is to provide the layers from the side farthest from the support in the order of a low blue-sensitive layer (BL)/a high blue-sensitive layer (BH)/a high green-sensitive layer (GH)/a low green-sensitive layer(GL)/a high red-sensitive layer (RH)/a low red-sensitive layer (RL), the order of BH/BL/GL/GH/RH/RL, or the order of BH/BL/GH/GL/RL/RH.
Further, the layers can be provided from the side farthest from the support in the order of a blue-sensitive layer/GH/R/{/GL/RL, as described in JP-B-55-34932. The layers can also be provided from the side farthest from the support in the order of a blue-sensitive layer/GL/RL/GH/PJ4, as described in JP-A-56-25738 and JP-A-62-63936. There can be given the structure of three layers having the different sensitivities, respectively, comprising a high sensitive silver halide emulsion layer provided on the uppermost side, a middle sensitive silver halide emulsion layer provided on an intermediate side, and a low sensitive silver halide emulsion layer provided on a lower side, as described in JP-B-49-15495, herein the sensitivity becomes lower toward the support, as described in JP-B-49-15495. Also in the case of the above structure of three layers having the different sensitivities, the layers having the same spectral sensitivity may be provided from the side farthest from the support in the order of an intermediate-sensitive emulsion layer/a high-sensitive emulsion layer/a low-sensitive emulsion layer, as described in JP-A-59-202464. Various layer structures and layer arrangements can be selected according to the purposes of the light-sensitive material as described above.
The dry thickness of the whole constituent layers excluding a support, subbing layer and a back layer, is preferably 12.0 to 20.0 .mu.m, more preferably 12.0 to 18.0 .mu.m from the viewpoint of bleaching fog and aging stain.
The film thickness of a light-sensitive material is measured in the following manner; at the light-sensitive material to be measured is stored for 7 days under conditions of 25.degree. C. and 50% RH after the preparation thereof; the whole thickness of the light-sensitive material is measured and then, after removing the layers coated on the support, the thickness of the light-sensitive material is measured once again; and the film thickness of the whole coated layers excluding the support of the above light-sensitive material is defined by the difference thereof. This thickness can be measured with a film thickness measuring device K-402B Stand, manufactured by Anritsu Electric Co., Ltd., using a contact type piezoelectric conversion element. The coated layers on the support can be removed with an aqueous sodium hypochlorite solution. The section of the light-sensitive material can be photographed with a scanning type electron microscope (magnification: preferably 3000 or more) to measure the whole layer thickness coated on the support.
In the present invention, the swelling rate is preferably 50 to 200%, more preferably 70 to 150%, wherein the swelling rate is defined by the following equation:
Swelling rate=(A-B)/B.times.100 (%)
A: equilibrium swollen film thickness in water at 25.degree. C.
B: total dry film thickness at 25.degree. C. and 55% RH.
The swelling rate derivating from the above limits increases the residual amount of the color developing agent and badly affects the photographic properties, the image quality such as the desilvering property and the film properties such as film strength.
Further, the swelling speed of the light-sensitive material represented by T 1/2 is preferably 15 seconds or less, more preferably 9 seconds or less, wherein T 1/2 is defined as the time spent until the swelling reaches one half of a saturated swollen film thickness which is defined as 90% of the maximum swollen film thickness attained when the light-sensitive material is processed in a color developing solution at 38.degree. C. for 3 minutes and 15 seconds.
Silver halides contained in the photographic emulsion layer of the light-sensitive material used in the present invention may be any of silver iodobromide, silver iodochlorobromide, silver chlorobromide, silver bromide and silver chloride.
Preferred silver halide is silver iodobromide, silver iodochloride or silver iodochlorobromide containing silver iodide in the amount of 0.1 to 30 mole %. Particularly preferred is silver iodobromide containing silver iodide in the amount of 2 to 25 mole %.
The silver halide grains contained in a photographic emulsion may be of a regular crystal such as cube, octahedron or tetradecahedron, an irregular crystal such as sphere or plate, a defective crystal such as twinned crystal, or a composite thereof.
Silver halide may comprise fine grains having a size of about 0.2 .mu.m or less, or large grains having a projected area diameter up to 10 .mu.m and a silver halide emulsion may be polydispersed or monodispersed.
The silver halide photographic emulsion used in the present invention can be prepared by the methods described in, for example, Research Disclosure (RD) No. 17643 (December 1978), pp. 22 to 23, "I. Emulsion Preparation and Types" and No. 18716 (November 1979), p. 648, Chimie et Physique Photographique, by P. Glafkides, published by Paul Morttel Co. (1967), Photographic Emulsion Chemistry, by G. F. Dufin, published by Focal Press Co. (1966), and Making and Coating Photographic Emulsion, by V. L. Zelikman el al, published by Focal Press Co. (1964).
Also preferred are the monodispersed emulsions described in U.S. Pat. Nos. 3,574,628 and 3,655,394, and British Patent 1,413,748. The tabular grains having an aspect ratio of 5 or more can also be used in the present invention. The tabular grains can be prepared by the methods described in Photographic Science and Engineering, by Gutoff, vol. 14, pp. 248 to 257 (1970), U.S. Pat. Nos. 4,434,226, 4,414,310, 4,430,048, and 4,439,520, and British Patent 2,112,157.
The crystal structure may be uniform or of a different halogen composition on the inside and a surface or of a stratum structure. Further, silver halides of different compositions may be conjugated with an epitaxial conjugation. Furthermore, silver halides may be conjugated with the compounds other than silver halides, such as silver rhodanide and lead oxide.
Further, a mixture of the grains having the different crystal forms may be used.
Usually, the silver halide emulsions are subjected to physical ripening, chemical ripening and spectral sensitization before use. The additives used in such steps are described in Research Disclosure, No. 17643 (December 1978), No. 18716 (November 1979) and No. 307105 (November 1989), and the corresponding passages are listed in the following table.
The publicly known photographic additives also are described in the above three Research Disclosures (RD) and the corresponding passages described therein are listed as well in the following table:
______________________________________Kind of Additives RD 17643 RD 18716 RD 307105______________________________________ 1. Chemical sensitizer p. 23 p. 648, p. 866 right col. 2. Sensitivity improver -- p. 648 -- right col. 3. Spectral sensitizer & pp. 23 p. 648 pp. 866 Super sensitizer to 24 right col. to 868 to p. 649 right col. 4. Whitening agent p. 24 p. 647 p. 868 right col. 5. Anti-foggant & pp. 24 p. 649 pp. 868 stabilizer to 25 right col. to 870 6. Light absorber, filter, pp. 25 p. 649 p. 873 dye, & UV absorber to 26 right col. to p. 650 left col. 7. Anti-stain agent p. 25 p. 650 p. 872 right col. left to right cols. 8. Dye image stabilizer p. 25 p. 650 p. 872 left col. 9. Hardener p. 26 p. 651 pp. 874 left col. to 87510. Binder p. 26 p. 651 pp. 873 left col. to 87411. Plasticize & lubricant p. 27 p. 650 p. 876 right col.12. Coating aid & pp. 26 p. 650 pp. 875 surfactant to 27 right col. to 87613. Anti-static agent p. 27 p. 650 pp. 876 right col. to 87714. Matting agent -- -- pp. 878 to 879______________________________________
In the present invention, various color couplers can be used in combination. Representative examples thereof are described in the patents described in above RD No. 17643, VII-C to G and RD No. 307105, VII-C to G.
Preferred are the yellow couplers described in, for example, U.S. Pat. Nos. 3,933,501, 4,022,620, 4,326,024, 4,401,752 and 4,248,961, JP-B-58-10739, British Patent 1,425,020 and 1,476,760, U.S. Pat. Nos. 3,973,968, 4,314,023, and 4,511,649, European Patent 249,473A, and JP-A-3-131847. Further, 1-alkylcyclopropylcarbonyl type or indolinylcarbonyl type yellow couplers having high absorptivity and high fastness to moisture and heat as described in, for example, Japanese Patent Application Nos. 2-64718, 2-314522, 2-232857, 2-26341 and 2-296401 are particularly preferred.
Diequivalent and/or tetraequivalent 5-pyrazolone type and pyrazoloazole type compounds are preferred as a magenta coupler. Further preferred are the compounds described in U.S. Pat. Nos. 4,310,619 and 4,351,897, European Patent 73,636, U.S. Pat. Nos. 3,061,432 and 3,725,064, RD No. 24220 (June 1984), JP-A-60-33552, RD No. 24230 (June 1984), JP-A-60-43659, JP-A-61-72238, JP-AS60-35730, JP-A-55-118034, and JP-A-60-185951, U.S. Pat. Nos. 4,500,630, 4,540,654, and 4,556,630, and WO (PCT) 88/04795.
In the present invention, the use of at least one kind of the tetraequivalent magenta coupler can provide marked effects.
Of the tetraequivalent magenta couplers, preferred are the tetraequivalent 5-pyrazolone type magenta couplers represented by the following formula (M) or the tetraequivalent pyrazoloazole type magenta couplers represented by the following formula (m): ##STR16## in formula (M), R.sub.4 represents an alkyl group, an aryl group, an acyl group, or a carbamoyl group; Ar represents a substituted or unsubstituted phenyl group, provided that either of R.sub.4 and Ar may be a polyvalent group having a divalency or a higher valency to form a polymer, such as a dimer, and that it may link a main coupling structure of the coupler with a principal chain of a polymer to form a polymer coupler; in formula (m), R.sub.5 represents a hydrogen atom or a substituent; and Z represents a group of non-metallic atoms necessary to form a 5-membered azole ring containing 2 to 4 nitrogen atoms, and the azole ring may have a substituent or a condensed ring, provided that either of R.sub.5 and Z may be a polyvalent group having a divalency or a higher valency to form a polymer, such as a diamer, and that it may link a main coupling structure of the coupler with a principal chain of a polymer to from a polymer coupler.
In R.sub.4 of formula (M), the alkyl group represents a linear or branched alkyl group having 1 to 42 carbon atoms, an aralkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, or a cycloalkenyl group; the aryl group represents an aryl group having 6 to 46 carbon atoms; the acyl group represents an aliphatic acyl group having 2 to 32 carbon atoms or an aromatic acyl group having 7 to 46 carbon atoms; and the carbamoyl group represents an aliphatic carbamoyl group having 2 to 32 carbon atoms or an aromatic carbamoyl group having 7 to 46 carbon atoms. These groups may have substituents, which are organic substituents having a carbon atom, oxygen atom, nitrogen atom or sulfur atom at a bonding site, or halogen atoms.
In more detail, R.sub.4 represents an alkyl group (for example, methyl, ethyl, butyl, propyl, octadecyl, isopropyl, t-butyl, cyclopeatyl, cyclohexyl, methoxyethyl, ethoxyethyl, t-butoxyethyl, phenoxyethyl, methanesulfonylethyl, and 2-(2,4-di-tert-amyphenoxy) ethyl); an aryl group (for example, phenyl, 2-chlorophenyl, 2-methoxyphenyl, 2-chloro-5-tetradecaneamidephenyl, 2-chloro-5-(3-octadecenyl-1-succinimide) phenyl, 2-choloro-5-octadecylsulfonamidephenyl, and 5-chloro-5-[2-(4-hydroxy-3-tert-butylphenoxy) tetradecanamidephenyl]); an acyl group (for example, acetyl, pivaloyl, tetradecanoyl, 2-(2,4-di-tert-pentylphenoxy) acetyl, 2-(2,4-di-tert-pentylphenoxy) butanoyl, benzoyl, and 3-(2,4-di-tert-amylphenoxyacetamide) benzoyl; a carbamoyl group (for example, N-methylcarbamoyl, N,N-dimethylcarbamoyl, N-hexadecylcarbamoyl, N-methyl-N-phenylcabamoyl, and N-[3-(1-(2,4-di-tert-phentylphenoxy) butylamide)] phenylcarbamoyl.
Examples of the substituents of these groups include an alkyl group, an aryl group, a heterocyclic group, a cyano group, a hydroxy group, a nitro group, a carboxy group, an amino group, an acyl group, an aryloxycarbonyl group, an alkoxycarboxy group, a carbamoyl group, an alkoxy group, an aryloxy group, a heterocyclicoxy group, an acyloxy group, a carbamoyloxy group, a silyloxy group, an aryloxycarbonylamino group, an acylamino group, an alkylamino group, an anilino group, a ureido group, a sufamoylamino group, an alkoxycarbonylamino group, a sulfonamide group, an aryloxycarbonylamino group, an imide group, an alkylthio group, an arylthio group, a heterocyclicthio group, a sulfamoyl group, a sulfonyl group, a sulfinyl group, an azo group, a phosphonyl group, an azolyl group, a fluorine atom, a chlorine atom, and a bromine atom. R.sub.4 is preferably an aryl group and an acyl group.
Ar in formula (M) represents a substituted or unsubstituted phenyl group. Preferred substituents include a halogen atom, an alkyl group, a cyano group, an alkoxy group, an alkoxycarbonyl group, and an acylamino group.
Ar is, for example, phenyl, 2,4,6-trichloropheyl, 2,5-dichlorophenyl, 2,4-dimethyl-6-methoxyphenyl, 2,6-dichloro-4-methoxyphenyl, 2,6-dichloro-4-ethoxycarbonylphenyl, 2,6-dichloro-4-cyanophenyl group, or4-[2-(2,4-di-tert-amylphenoxy) butylamide] phenyl. Ar is preferably a substituted phenyl group, more preferably a phenyl group which is substituted with at least one halogen atom (particularly a chlorine atom) and particularly preferably 2,4,6-trichlorophenyl or 2,5-dichlorophenyl.
Of the pyrazoloazole type magenta couplers represented by formula (m), preferred are the compounds having the skeletal structure of 1H-imidazo [1,2-b] pyrazole, 1H-pyrazolo [1,5-b] [1,2,4] triazole, 1H-pyrazolo [5,1-c] [1,2,4] triazole, or 1H-pyrazolo [1,5-d] tetrazole. They are represented by the following formulas (m-1), (m-2), (m-3) and (m-4), respectively: ##STR17##
R.sub.5, R.sub.51, R.sub.52, and R.sub.53, in formula (m) and these formulas are explained below.
R.sub.5 and R.sub.51 represent independently a hydrogen atom and a substituent. The substituent may be a halogen atom, an alkyl group, an aryl group, a heterocyclic group, a cyano group, a hydroxy group, a sulfo group, a nitro group, a carboxy group, an amino group, an alkoxy group, an aryloxy group, an acylamino group, an alkylamino group, an anilino group, a ureido group, a sulfamoylamino group, an alkylthio group, an arylthio group, an alkoxycarbonylamino group, a sulfonamide group, a carbamoyl group, a sulfamoyl group, a sulfonyl group, an alkoxycarbonyl group, a heterocyclicoxy group, an azo group, an acryloxy group, a carbamoyloxy group, a silyloxy group, an aryloxycarbonylamino group, an imide group, a heterocyclicthio group, a sulfinyl group, a phosphonyl group, an aryloxycarbonyl group, an acyl group, and an azolyl group. R.sub.5 and R.sub.51 may be divalent to form a bis product.
In further detail, R.sub.5 and R.sub.51 represent independently a hydrogen atom, a halogen atom (for example, a chlorine atom and a bromine atom), an alkyl group (for example, a linear or branched alkyl group having 1 to 32 carbon atoms, an aralkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, and a cyaloalkenyl group, and more specifically, methyl, ethyl, propyl, isopropyl, t-butyl, tridecyl, 2-methanesulfonylethyl, 3-(3-pentadecylphenoxy) propyl, 3-{4-{2-[4-(4-hydroxyphenylsulfonyl) phenoxy] dodecanamide} phenyl} propyl, 2-ethoxytridecyl, trifluoromethyl, cyclopentyl, and 3-(2,4-di-tert-amylphenoxy) propyl), an aryl group (for example, phenyl, 4-t-butylphenyl, 2,4-di-t-amylphenyl, and 4-tetradecananidephenyl), a heterocyclic group (for example, 2-furyl, 2-thienyl, 2-pyrimidinyl, and 2-benzothiazolyl), a cyano group, a hydroxy group, a sulfo group, a nitro group, a carboxy group, an amino group, an alkoxy group (for example, methoxy, ethoxy, 2-methoxyethoxy, 2-dodecyloxyethoxy, and 2-methanesulfonylethoxy), an aryloxy group (for example, phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3-nitrophenoxy, 3-t-butyloxycarbamoylphenoxy, and 3-methoxycarbamoylphenoxy), an acylamino group (for example, acetamide, benzamide, tetradecanamide, 2-(2,4-di-t-amylphenoxy) butanamide, 4- (3-t-butyl-4-hydroxyphenoxy) butanamide, and 2-[4-(4hydroxyphenylsufonyl) phenoxy] decanamide), an alkylamino group (for example, methylamino, butylamino, dodecylamino, diethylamino, and methylbutylamino ), an anilino group (for example, phenylamino, 2-chloroanilino, 2-chloro-5-tetradecanaminoanilino, 2-chloro-5-dodecyloxycarbonylanilino, N-acetylanilino, and 2-chloro-5- [.alpha.- (3-t-butyl-4-hydroxyphenoxy) dodecaneamide ] anilino), a ureido group (for example, phenylureido, methylureido and N, N-dibutylureido ), a sulfamoylamino group (for example, N,N-dipropylsulfamoylamino, and N-methyl-N-decylsulfamoylamino ), an alkylthio group (for example, methylthio, octylthio, tetradecylthio, 2-phenoxyethylthio, 3-phenoxypropylthio, and 3-(4-t-butylphenoxy) propylthio), an arylthio group (for example, phenylthio, 2-butoxy-5-t-octylphenylthio, 3-pentadecylphenylthio, 2-carboxynylthio, and 4 -tetradecanamidephenylthio), an alkoxycarbonylamnino group (for example, methoxycarbonylamino and tetradecyloxycarbonylamino), a sulfonamide group (for example, methanesulfonamide, hexadecanesulfonamide, benzenesulfonamide, p-toluenesulfonamide octadecanesul fonamide, and 2-methoxy-5-t-butylbenzenesulfonamide), a carbamoyl group (for example, N-ethylcarbamoyl, N, N-dibutylcarbamoyl, N- (2-dodecyoxyethyl carbamoyl, N-methyl-N-dodecylcarbamoyl, and N-[3-(2,4-di-t-amylphenoxy) propyl] carbamoyl), a sulfamoyl group (for example, N-ethylsulfamoyl, N,N-dipropylsulfamoyl, N-(2-dodecyloxyethyl) sulfamoyl, N-ethyl-N-dodecylsulfamoyl, and N,N-diethylsulfamoyl), a sulfonyl group (for example, methanesulfonyl, octanesulfonyl, benzenesulfonyl, and toluenesulfonyl), an alkoxycarbonyl group (for example, methoxycarbonyl, butyloxycarbonyl, dodecyloxycarbonyl, and octadecyloxycarbonyl), a heterocyclicoxy group (for example, 1-phenyltetrazole-5-oxy, and 2-tetrahydropyranyloxy), an azo group (for example, phenylazo, 4-methoxyphenylazo, 4-pivaloylaminophenylazo, and 2-hydroxy-4-propanoylphenylazo),an acyloxy group (for example, acetoxy), a carbamoyloxy (for example, N-methylcarbamoyloxy and N-phenylcarbamoyloxy), a silyloxy group (for example, trimethylsilyloxy and dibutylmethylsilyloxy), an aryloxycarbonylamino group (for example, phenoxycarbonylamino), an imide group (for example, N-succinimide, N-phthalimide, and 3-octadecenylsuccinimide), a heterocyclicthio group (for example, 2-benzothiazolylthio, 2,4-di-phenoxy-1,3,5-triazole-6-thio, and 2-pyridylthio), a sulfinyl group (for example, dodecanesulfinyl, 3-sulfinyl pentadecylphenylsulfinyl, and 3-phenoxypropylsulfinyl), a phosphonyl group (for example, phenoxyphosphonyl, octyloxyphosphonyl, and phenylphosphonyl), an aryloxycarbonyl group (for example, phenoxycarbonyl), an acyl group (for example, acetyl, 3-phenylpropanoyl, benzoyl, and dodecyloxybenzoyl), and an azolyl group (for example, imidazolyl, pyrazolyl, 3-chloro-pyrazole-1-yl, and triazoyl).
Of these groups, the groups capable of having further substituents may have the organic substituents linked with a carbon atom, an oxygen atom, a nitrogen atom or a sulfur atom, or a halogen atom.
Of these groups, the preferred groups represented by R.sub.5 and R.sub.51 are an alkyl group, an aryl group, an alkoxy group, an aryloxy group, an alkylthio group, a ureido group, a carbomoyloxy group, and an acylamino group.
R.sub.52 represents the same groups as those defined for R.sub.51, and preferred are a hydrogen atom, an alkyl group, an aryl group, a heterocyclic group, an alkoxycarbonyl group, a carbamoyl group, a sulfamoyl group, a sulfinyl group, an acyl group, and a cyano group.
R.sub.53 represents the same groups as those defined for R.sub.51, and preferred are a hydrogen atom, an alkyl group, an aryl group, a heterocyclic group, an alkoxy group, an aryloxy group, an alkylthio group, and arylthio group, an alkoxycarbonyl group, a carbamoyl group, and an acyl group. More preferred are an alkyl group, an aryl group, a heterocyclic group, an alkylthio group, and an arylthio group.
The magenta couplers represented by formulas (m-1), (m-2), (m-3) and (m-4) can be synthesized by the methods disclosed in U.S. Pat. Nos. 4,540,654, 4,705,863, 3,725,067, 2,710,871, 3,684,514, 3,928,044 and 3,928,044.
The polymer product of the magenta coupler of formula (M) or (m) is disclosed in JP-B-2-44051.
Examples of the tetraequivalent magenta coupler are shown below: ##STR18##
In the above, the ratios of repeating units are by weight.
The use of the tetraequivalent 5-pyrazolone type magenta coupler of formula (M) can particularly demonstrate the effects of the present invention.
In the present invention, the coated amount of the tetraequivalent magenta coupler is preferably 0.4.times.10.sup.-3 to 3.5.times.10.sup.-3 mole per m.sup.2 of the light-sensitive material. This coupler can be used in combination with a diequivalent magenta coupler without causing any problem.
There can be mentioned as a cyan coupler the phenol and naphthol type couplers. Preferred are the compounds described in U.S. Pat. Nos. 4,052,212, 4,146,396, 4,228, 233, 4,296,200, 2,369,929, 2,801,171, 2,772,162, 2,895,826, 3,772,002, 3,758,308, 4,334,011, and 4,327,173; German Patent (OLS) 3,329,729; European Patents 121,365A, and 249,453A; U.S. Pat. Nos. 3,446,622, 4,333,999, 4,753,871, 4,451,559, 4,427,767, 4,690,889, 4,254,212, and 4,296,199; and JP-A-61-42658, and JP-A-3-196037. Particularly preferred are pyrrolotriazole, pyrroloimidazole, imidazopyrazole, imidazole, pyrazolotriazole, and cyclic active methylene type cyan couplers described in Japanese Patent Application Nos. 2-302078, 2-322051, 3-226325, and 3-236894, JP-A-32260 and JP-A-2-141745.
Preferred as a colored coupler used for correcting any unnecessary absorption of a formed image are the compounds described in RD No. 17643, VII-G, U.S. Pat. No. 4,163,670, JP-B-57-39413, U.S. Pat. Nos. 4,004,929 and 4,138,258, British Patent 1,146,368, and Japanese Patent Application No. 2-50137. Also, preferably used are the couplers which correct any unnecessary absorption of a formed image with a fluorescent dye released in coupling, described in U.S. Pat. No. 4,774,181, and the couplers having as a releasing group a dye precursor group capable of reacting with a developing agent to form a dye, described in U.S. Pat. No. 4,777,120.
Preferred as a coupler capable of forming a dye having an appropriate diffusing property are the compounds descried in U.S. Pat. No. 4,366,237, British Patent 2,125,570, European Patent 96,570, and German Patent (OLS) 3,234,533.
The typical examples of a dye-forming polymer coupler are described in U.S. Pat. Nos. 3,451,820, 4,080,211, 4,367,282, 4,409,320, and 4,576,910, and British Patent 2,102,173.
Also, there can be preferably used a coupler releasing a photographically useful residue by coupling. Preferred as a coupler releasing imagewise a nucleus-forming agent or a development accelerator in developing are the couplers described in British Patents 2,097,140 and 2,131,188, and JP-A-59-157638 and JP-A-59-170840.
In addition to the above, there are given as couplers capable of being used in light-sensitive material, the competitive couplers described in U.S. Pat. No. 4,130,427; the couplers releasing a dye whose color is recovered after releasing, described in European Patent 173,302A; the bleaching accelerator-releasing couplers described in RD No. 11449 and 24241, and JP-A-61-201247; the ligand-releasing couplers described in U.S. Pat. No. 4,553,477; the couplers releasing a leuco dye described in JP-A-63-75747; and the couplers releasing a fluorescent dye described in U.S. Pat. No. 4,774,181.
The couplers used in the present invention can be incorporated into a light-sensitive material by various conventional dispersing methods.
Examples of a high boiling-solvent used in an oil-in-water dispersion method are described in U.S. Pat. No. 2,322,027. Representative examples of the high-boiling organic solvent which has a boiling point at normal pressure of 175.degree. C. or higher and is used in the oil-in-water dispersion method include phthalic 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, and bis(1,1-diethylpropyl) phthalate), phosphoric or phosphonic esters (triphenyl phosphate, tricresyl phosphate, 2-ethylhexyldiphenyl phosphate, tricyclohexyl phosphate, tri-2-ethylhexyl phosphate, tridodecyl phosphate, tributoxyethyl phosphate, trichloropropyl phosphate, and di-2-ethylhexyl phosphonate), benzoic esters (2-ethylhexyl benzoate, dodecyl benzoate, and 2-ethylhexyl-p-hydroxybenzoate), amides (N,N-diethyldecanamide, N,N-diethyllaurylamide, and N-tetradecylpyrrolidone), alcohols and phenols (isostearyl alcohol and 2,4-di-tert-amylphenol), aliphatic carboxylic esters (bis(2-ethylhexyl) sebacate, dioctyl azelate, glycerol tributylate, isostearyl lactate, and trioctyl citrate), aniline derivatives (N,N-dibutyl-2-butoxy-5-tert-octyl-aniline), and hydrocarbons (paraffin, dodecylbenzene, and diisopropylnaphthalene).
There can be used as an auxiliary solvent, organic solvents having a boiling point of about 30.degree. C. or higher, preferably 50.degree. C. or higher and about 160.degree. C. or lower. Typical examples thereof include ethyl acetate, butyl acetate, ethyl propionate, methyl ethyl ketone, cyclohexanone, 2-ethoxyethyl acetate, and dimethylformamide.
Concrete examples of the steps and effect of a latex dispersing method and latexes for impregnation are described in U.S. Pat. No. 4,199,363, and German Patents (OLS) 2,541,274 and 2,541,230.
These couplers can be dispersed and emulsified in a hydrophilic colloid solution after they are impregnated into a loadable latex in the presence or absence of a high-boiling organic solvent (for example, U.S. Pat. No. 4,203,716), or they can be dissolved in a water insoluble and organic solvent-soluble polymer. Preferably used is a homopolymer or copolymer described on pages 12 to 30 of the specification of International Publication No. W088/00723. Particularly, a polyacrylamide type polymer is preferably used in terms of stabilizing a dye image.
A support suitable for use in the present invention is described in, for example, RD No. 17643, p. 28 and No. 18716, p. 647, right column to p. 648, left column.
The present invention can be applied to various light-sensitive materials. Particularly, it is used preferably for color negative films for general purpose and cinema and reversal films for slide and TV.
EXAMPLES
The present invention will be explained in detail with reference to the following examples, but not is limited thereto.
EXAMPLE 1
Layers having the following compositions were provided on a cellulose triacetate film support having thereon a subbing layer to prepare a multi-layered color light-sensitive material Sample No. 101.
Composition of a light-sensitive layer
The coated amounts are expressed in terms of g/m.sup.2 of silver for silver halide and colloidal silver, in terms of g/m.sup.2 for the couplers, additives and gelatin, and in terms of mole per mole of silver halide for the spectral sensitizers.
______________________________________First layer: an anti-halation layerBlack colloidal silver 0.20Gelatin 2.20UV-1 0.11UV-2 0.20Cpd-1 4.0 .times. 10.sup.-2Cpd-2 1.9 .times. 10.sup.-2Solv-1 0.30Solv-2 1.2 .times. 10.sup.-2Second layer: an intermediate layerSilver iodobromide fine grains 0.15(AgI: 1.0 mole %, circle-correspondingdiameter: 0.07 .mu.m)Gelatin 1.00ExC-4 6.0 .times. 10.sup.-2Cpd-3 2.0 .times. 10.sup.-2Third layer: the first red-sensitive layerSilver iodobromide emulsion 0.42AgI: 5.0 mole %, higher AgI content on surface, circle-corresponding diameter: 0.9 .mu.m, fluctuation coefficient ofcircle-corresponding diameter: 21%, tabular grains,diameter/thickness ratio: 7.5)Silver iodobromide emulsion 0.40AgI: 4.0 mole %, higher AgI content in inside, circle-corresponding diameter: 0.4 .mu.m, fluctuation coefficient ofcircle-corresponding diameter: 18%, tetradecahedron grains)Gelatin 1.90ExS-1 4.5 .times. 10.sup.-4ExS-2 1.5 .times. 10.sup.-4ExS-3 4.0 .times. 10.sup.-5ExC-1 0.65ExC-3 1.0 .times. 10.sup.-2ExC-4 2.3 .times. 10.sup.-2Solv-1 0.32Fourth layer: the second red-sensitive layerSilver iodobromide emulsion 0.85AgI: 8.5 mole %, higher AgI content in inside, circle-corresponding diameter: 1.0 .mu.m, fluctuation coefficient ofcircle-corresponding diameter: 25% tabular grains,diameter/thickness ratio: 3.0)Gelatin 0.91ExS-1 3.0 .times. 10.sup.-4ExS-2 1.0 .times. 10.sup.-4ExS-3 3 0 .times. 10.sup.-5ExC-1 0.13ExC-2 6.2 .times. 10.sup.-2ExC-4 4.0 .times. 10.sup.-2Solv-1 0.10Fifth layer: the third red-sensitive layerSilver iodobromide emulsion 1.50AgI: 11.3.mole %, higher AgI content in inside, circle-corresponding diameter: 1.4 .mu..mu.m, fluctuation coefficient ofcircle-corresponding diameter: 28%, tabular grains,diameter/thickness ratio: 6.0)Gelatin 1.20ExS-1 2.0 .times. 10.sup.-4ExS-2 6.0 .times. 10.sup.-5ExS-3 2 0 .times. 10.sup.-5ExC-2 8.5 .times. 10.sup.-2ExC-5 7.3 .times. 10.sup.-2Solv-1 0.12Solv-2 0.12Sixth layer: an intermediate layerGelatin 1.00Cpd-4 8.0 .times. 10.sup.-2Solv-1 8.0 .times. 10.sup.-2 Seventh layer: the first green-sensitive layerSilver iodobromide emulsion 0.28AgI: 5.0 mole %, higher AgI content on surface, circle-corresponding diameter: 0.9 .mu.m, fluctuation coefficient ofcircle-corresponding diameter: 21%, tabular grains,diameter/thickness ratio: 7.5)Silver iodobromide emulsion 0.16AgI: 4.0 mole %, higher AgI content in inside, circle-corresponding diameter: 0.4 .mu.m, fluctuation coefficient ofcircle-corresponding diameter: 18%, tetradecahedron grains)Gelatin 1.20ExS-4 5.0 .times. 10.sup.-4ExS-5 2.0 .times. 10.sup.-4ExS-6 1.0 .times. 10.sup.-4ExM-1 0.50ExM-2 0.10ExM-5 3.5 .times. 10.sup.-2Solv-1 0.20Solv-2 0.20Solv-3 3.0 .times. 10.sup.-2Eighth layer: the second green-sensitive layerSilver iodobromide emulsion 0.57AgI: 8.5 mole %, higher AgI content in inside, circle-corresponding diameter: 1.0 .mu.m, fluctuation coefficient ofcircle-corresponding diameter: 25%, tabular grains,diameter/thickness ratio: 3.0)Gelatin 0.45ExS-4 3.5 .times. 10.sup.-4ExS-5 1.4 .times. 10.sup.-4ExS-6 7.0 .times. 10.sup.-5ExM-1 0.12ExM-2 7.1 .times. 10.sup.-3ExM-3 3.5 .times. 10.sup. -2Solv-1 0.15Solv-3 1.0 .times. 10.sup.-2Ninth layer: an intermediate layerGelatin 0.50Solv-1 2.0 .times. 10.sup.-2Tenth layer: the third green-sensitive layerSilver iodobromide emulsion 1.30AgI: 11.3 mole %, higher AgI content in inside, circle-corresponding diameter: 1.4 .mu.m, fluctuation coefficient ofcircle-corresponding diameter: 28%, tabular grains,diameter/thickness ratio: 6.0)Gelatin 1.20ExS-4 2.0 .times. 10.sup.-4ExS-5 8.0 .times. 10.sup.-5ExS-6 8.0 .times. 10.sup.-5ExM-4 4.5 .times. 10.sup.-2ExM-6 1.0 .times. 10.sup.-2ExC-2 4.5 .times. 10.sup.-3Cpd-5 1.0 .times. 10.sup.-2Solv-1 0.25Eleventh layer: a yellow filter layerGelatin 0.50Cpd-6 5.2 .times. 10.sup.-2Solv-1 0.12Twelfth layer: an intermediate layerGelatin 0.45Cpd-3 0.10Thirteenth layer: the first blue-sensitive layerSilver iodobromide emulsion 0.20AgI: 2 mole %, uniform AgI content, circle-correspondingdiameter: 0.55 .mu.m, fluctuation coefficient of circle-corresponding diameter: 25%, tabular grains,diameter/thickness ratio: 7.0)Gelatin 1.00ExS-7 3.0 .times. 10.sup.-4ExY-1 0.60ExY-2 2.3 .times. 10.sup.-2Solv-1 0.15Fourteenth layer: the second blue-sensitive layerSilver iodobromide emulsion 0.19AgI: 19.0 mole %, higher AgI content in inside, circle-corresponding diameter: 1.0 .mu.m, fluctuation coefficient ofcircle-corresponding diameter: 16%, octahedron grains)Gelatin 0.35ExS-7 2.0 .times. 10.sup.-4ExY-1 0.22Solv-1 7.0 .times. 10.sup.-2Fifteenth layer: an intermediate layerSilver iodobromide fine grains 0.20AgI: 2 mole %, uniform AgI content, circle-correspondingdiameter: 0.13 .mu.m)Gelatin 0.36Sixteenth layer: the third blue-sensitive layerSilver iodobromide emulsions 1.55AgI: 14.0 mole %, higher AgI content in inside, circle-corresponding diameter: 1.7 .mu.m, fluctuation coefficient ofcircle-corresponding diameter: 28%, tabular grains,diameter/thickness ratio: 5.0)Gelatin 1.00ExS-8 1.5 .times. 10.sup.-4ExY-1 0.21Solv-1 7.0 .times. 10.sup.-2Seventeenth layer: the first protective layerGelatin 1.80UV-1 0.13UV-2 0.21Solv-1 1.0 .times. 10.sup.-2Solv-2 1.0 .times. 10.sup.-2Eighteenth layer: the second protective layerSilver chloride fine grains 0.36(Circle-corresponding diameter: 0.07 .mu.m)Gelatin 0.70B-1 (diameter: 1.5 .mu.m) 2.0 .times. 10.sup.-2B-2 (diameter: 1.5 .mu.m) 0.15B-3 3.0 .times. 10.sup.-2W-1 2.0 .times. 10.sup.-2H-1 0.35Cpd-7 1.00______________________________________
There were added to this sample, 1,2-benzoisothiazoline-3-one (average 200 ppm to gelatin), n-butyl-p-hydroxybenzoate (about 1,000 ppm to gelatin), and 2-phenoxyethanol (about 10,000 ppm to gelatin). Further, the sample contained therein, B-4, B-5, W-2, W-3, F-1, F-2, F-3, F-4, F-5, F-6, F-7, F-8, F-9 F-10, F-11, F-12, F-13, iron salts, lead salts, gold salts, platinum salts, iridium salts, and rhodium salts.
The above compounds used are shown below. ##STR19##
The dry layer thickness excluding that of the support of above Sample 101 was 22 .mu.m and the swelling speed T 1/2 was 9 seconds.
Sample No. 101 thus prepared was cut to a length of 2 meter with a width of 35 mm. A cut sample was exposed to white light of 50 lux for 0.01 second and then was processed with an automatic developing machine under the following conditions so that the accumulated replenishing amount of the processing solutions was three times as large as that of the tank capacity. Only a stabilizing solution was exchanged in turn, and the respective processings were carried out under the same conditions. After stain of the processed sample was evaluated, it was subjected to a test of its image stabilizing property.
The processing steps and the compositions of the processing solutions are shown below.
______________________________________Processing steps Processing Replenish- Tank Processing temperature ing amount capacityStep time (.degree.C.) (ml) (l)______________________________________Color 3 minutes & 38.0 600 17developing 5 secondsBleaching 50 seconds 38.0 140 5Bleach- 50 seconds 38.0 -- 5fixingFixing 50 seconds 38.0 420 5Washing 30 seconds 38.0 980 3Stabilizing 20 seconds 38.0 -- 3(1)Stabilizing 20 seconds 38.0 560 3(2)Drying 1 minute 60______________________________________ Note: replenishing amount: per m.sup.2 of the lightsensitive material
The stabilizing solution flowed from (2) to (1) in a counter-current system and all of an overflowed solution of washing water was introduced into a fixing bath. All of the overflowed solution effluent from the breaching bath and fixing bath by supplying the replenishing solutions thereto flowed into the bleach-fixing bath as a replenishing solution. The carried-over amounts of the developing solution to the bleaching bath, the bleaching solution to the bleach-fixing bath, the bleach-fixing solution to the fixing bath and the fixing solution to the washing bath were 65, 50, 50 and 50 ml per m.sup.2 of the light-sensitive material, respectively. The crossover time was 6 seconds for each and this time was included in the processing time of the preceding bath.
The same solutions as the respective tank solutions were used as the replenishing solutions.
The compositions of the processing solutions are shown below. The unit is gram unless otherwise described.
______________________________________Color Developing solutionDiethylenetriaminepentaacetic acid 2.01-Hydroxyethylidene-1,1-diphosphonic acid 3.3Sodium sulfite 3.9Potassium carbonate 37.5Potassium bromide 1.4Potassium iodide 1.3 mgHydroxylamine sulfate 2.42-Methyl-4-[N-ethyl-N-(.beta.-hydroxyethyl) 4.5amino] aniline sulfateWater was added to make the total quantity 1 lpH 10.05Bleaching solutionFerric ammonium 1,3-diaminopropanetetraacetic 130acid monohydrateAmmonium bromide 80Ammonium nitrate 15Hydroxyacetic acid 50Acetic acid 40Water was added to make the total quantity 1 lpH was adjusted with aqueous ammonia to 4.2______________________________________
Bleach-fixing solution
The mixed solution of the above bleaching solution and the following fixing solution in the ratio of 15 to 85 by volume. pH: 7.0.
______________________________________Fixing solutionAmmonium sulfite 19Ammonium thiosulfate aqueous solution (700 g/liter) 280 mlImidazole 15Ethylenediaminetetraacetic acid 15Water was added to make the total quantity 1 lpH (adjusted with aqueous ammonia and acetic acid) 7.4______________________________________Washing water
Washing water
Tap water was introduced into a mixed-bed type column filled with H type strong acidic cation exchange resins (Amberlite IR-120B manufactured by Roban & Haas Co., Ltd.) and OH type strong base anion exchange resins (Amberlite IRA-400 manufactured by Rohm & Hass Co., Ltd.) to reduce the ion concentrations of calcium and magnesiumto 3 mg/l or less, and subsequently sodium dichloroisocyanurate 20 mg/l and sodium sulfate 150 mg/l were added. The pH range of this solution was 6.5 to 7.5.
______________________________________Stabilizing solutionSodium p-toluenesulfinate 0.1Polyoxyethylene-p-monononylphenyl ether 0.2(average polymerization degree: 10)ethylenediaminetetraacetate 0.05Image stabilizer (described in Table A) 0.01 moleWater was added to make the total quantity 1 lpH 7.2______________________________________
Evaluation of image preservability
The magenta densities of the respective samples thus processed were measured with a densitometer FSD 103 manufactured by Fuji Photo Film Co., Ltd. Then, each of the samples was subjected to an again test under the conditions of 25.degree. C. and a relative humidity of 55% for two months and the magenta densities were measured once again in the same manner to obtain the reductions thereof by aging (M fading), wherein the magenda densities of the respective samples after processing were 1.5.
Evaluation of processing stain
Each of the above samples after processing was visually observed to evaluate processing stain. The evaluation results were classified in five ranks:
Rank 1: No stains observed
2: Only a little bit of stain observed (one tenth or less of the sample surface was stained with a slight could)
3: Cloud observed on one tenth or more of the sample surface
4: Substances observed stuck on one tenth or less of the sample surface
5: Substances observed stuck on one tenth or more of the sample surface
Measurement of a formaldehyde vapor concentration
Each 100 ml of the stabilizing solutions prepared by the following procedure was put in a dish (an opening area: 80 cm.sup.2), which was settled in a closed glass vessel with a volume of five liters and was left to stand at 20.degree. C. for seven days. Then, the formaldehyde vapor concentration in the glass vessel was measured with an instant reading L type formaldehyde gas detecting tube manufactured by Gastech Co. (HCHO concentration).
The evaluation results are shown in Table A together with the image stabilizing agents used.
TABLE A______________________________________ Formaldehyde Image Vap. Conc.Sample No. Stabilizer M Fading Stain (ppm)______________________________________ 1 (Comp.) -- 0.30 1 -- 2 (Comp.) formaldehyde 0.00 1 5 or more 3 (Comp.) Comp. 0.19 5 5 or more Compound (h) 4 (Comp.) THHT*.sup.1 0.02 2 5 or more 5 (Comp.) NMP*.sup.2 0.18 3 0.4 6 (Comp.) NDH*.sup.3 0.25 3 5 or more 7 (Comp.) HMT*.sup.4 0.27 3 0.1 or less 8 (Inv.) I-1*.sup.5 0.00 1 0.5 9 (Inv.) I-2*.sup.5 0.01 1 0.610 (Inv.) I-3*.sup.5 0.01 1 0.611 (Inv.) I-4*.sup.5 0.01 1 0.612 (Inv.) I-5*.sup.5 0.02 2 0.713 (Inv.) I-26*.sup.5 0.02 1 0.714 (Inv.) I-27*.sup.5 0.02 1 0.8______________________________________ *.sup.1 THHT: tris (2hydroxyethyl)-1,3,5-hexahydro-s-triazine *.sup.2 NMP: Nmethylolpyrole *.sup.3 NDH: N, Ndimethylolhydantoin (*.sup.1, *.sup.2 & *.sup.3 describe in JPA-2-153348) *.sup.4 HMT: hexamethylenetetramine (described in JPA-63-44036) *.sup.5 Compound of the present invention
As can be found from the results shown in Table A, the use of the N-methylol compounds of the present invention can provide the processing method in which the vapor concentration of formaldehyde is reduced, the processed samples have no stains and an excellent image preservability can be attained.
EXAMPLE 2
Sample No. 201 was prepared in the same manner as in the preparation of Sample No. 101 of Example 1, except that ExC-6 shown below was further added to the fifth layer in an amount of 1.0.times.10.sup.-2 g/m.sup.2 and ExM-4 used in the tenth layer was replaced with ExM-4' shown below in the equal amount. ##STR20##
The thus prepared Sample No. 201 was processed in the same manner as in Example 1 except that the image stabilizer used in stabilizing solution was changed shown in Table B, and then was evaluated with respect to the image preservability, processing stain and formaldehyde vapor concentration in the same manner as in Example 1. The results are shown in Table B below.
TABLE B______________________________________ Formaldehyde Image Vap. Conc.Sample No. Stabilizer M Fading Stain (ppm)______________________________________ 1 (Comp.) -- 0.33 1 -- 2 (Comp.) formaldehyde 0.00 1 5 or more 3 (Comp.) Comp. 0.20 3 5 or more Compound (a) 4 (Comp.) Comp. 0.21 5 5 Compound (b) 5 (Comp.) Comp. 0.22 3 4 Compound (c) 6 (Comp.) Comp. 0.23 3 5 Compound (d) 7 (Comp.) Comp. 0.26 5 5 or more Compound (e) 8 (Comp.) Comp. 0.25 5 5 or more Compound (f) 9 (Comp.) Comp. 0.24 3 5 or more Compound (g)10 (Comp.) Comp. 0.20 5 5 or more Compound (h)11 (Comp.) Comp. 0.05 3 5 or more Compound (i)12 (Comp.) Comp. 0.30 3 0.5 or less Compound (j)13 (Comp.) Comp. 0.25 3 5 or more Compound (k)14 (Comp.) Comp. 0.24 4 5 or more Compound (l)15 (Comp.) Comp. 0.21 1 5 or more Compound (m)16 (Inv.) II-1 0.02 1 0.917 (Inv.) II-2 0.05 1 0.118 (Inv.) II-7 0.05 1 0.119 (Inv.) II-4 0.02 1 0.420 (Inv.) II-5 0.02 1 0.521 (Inv.) II-12 0.03 1 0.622 (Inv.) II-21 0.02 1 0.623 (Inv.) II-26 0.02 1 0.5______________________________________
Comparative Compounds (a) to (h) are disclosed above. ##STR21##
As can be found from the results shown in Table B, the use of the N-methylol compounds of the present invention can provide the processing method in which the vapor concentration of formaldehyde is reduced, the processing samples have no stains and an excellent image preservability can be attained.
EXAMPLE 3
Sample Nos. 201 and 202 were prepared in the same manner as Example 1, except that the magenta coupler ExM-1 of Sample No. 101 was replaced with equimolar M-1 and M-17, respectively. The samples thus prepared were evaluated in the same manner as in Example 1, and the similar results were obtained.
Further, Sample Nos. 203 and 204 were prepared in the same manner as Example 1, except that the magenta coupler ExM-4 of Sample No. 101 was replaced with equimolar M-1 and an equimolar mixture of ExM-4 and M-1 (1:1), respectively and they were evaluated in the same manner as Example 1 to obtain the similar results.
EXAMPLE 4
Sample No. 101 of Example 1 was processed in the following processing steps and solutions with an automatic developing machine. The processing was continued so that the accumulated replenishing amount of the stabilizing solution was three times as large as that of the tank capacity in Examples 1 and 2. The test of image preservability was carried out and the similar results were obtained.
______________________________________Processing steps Processing Replenishing Tank Processing Temperature Amount CapacityStep Time (.degree.C.) (ml) (l)______________________________________Color 3 minutes & 38 33 20developing 15 secondsBleaching 6 minutes & 38 25 40 30 secondsWashing 2 minutes & 24 1200 20 10 secondsFixing 4 minutes & 38 25 30 20 secondsWashing 1 minute & 24 -- 10(1) 5 secondsWashing 1 minute 24 1200 10(2)Stabilizing 1 minute & 38 25 10 5 secondsDrying 4 minutes & 55 20 seconds______________________________________ Note: Replenishing amount is per 1 m .times. 35 mm (width). Washing was done in a counter current system from (2) to (1).
The compositions of the processing solutions are shown below. The unit is gram unless otherwise described.
______________________________________ A B______________________________________Color Developing Solution (unit: g)Diethylenetriaminepentaacetic acid 1.0 1.11-Hydroxyethylidene-1,1-diphosphonic acid 3.0 3.2Sodium sulfite 4.0 4.4Potassium carbonate 30.0 37.0Potassium bromide 1.4 0.7Potassium iodide 1.5 mg --Hydroxylamine sulfate 2.4 2.84-[N-ethyl-N-(.beta.-hydroxyethylamino)] 4.5 5.52-methylaniline sulfateWater was added to make the total quantity 1 l 1 lpH 10.05 10.10Bleaching solutionFerric sodium ethylenediaminetetraacetic 100.0 120.0acid trihydrateDisodium ethylenediaminetetraacetic acid 10.0 10.0Ammonium bromide 140.0 160.0Ammonium nitrate 30.0 35.0Aqueous ammonia (27%) 6.5 ml 4.0 mlWater was added to make the total quantity 1 l 1 lpH 6.0 5.7Fixing solutionDisodium ethylenediaminetetraacetate 0.5 0.7Sodium sulfite 7.0 8.0Sodium bisulfite 5.0 5.5Ammonium thiosulfate aqueous solution 170.0 ml 200.0 ml(700 g/l)Water was added to make the total quantity 1.0 l 1.0 lpH 6.7 6.6Stabilizing solutionImage stabilizer (described in Tables A 2.0 ml 3.0 mland B)Polyoxyethylene-p-monononylphenyl ether 0.3 0.45(average polymerization degree: 10)Disodium ethylenediaminetetraacetate 0.05 0.08Water was added to make the total quantity 1.0 l 1.0 lpH 5.0-8.0 5.0-8.0______________________________________ Note: A: mother solution B: replenishing solution
EXAMPLE 5
Sample No. 101 of Example 1 was processed in Stabilizing Solution No. 1 (containing no image stabilizer) of Example 4 and the bleaching solution prepared by adding Compound I-1 (0.3 mole/liter) to the bleaching solution of Example 4. The processed sample was subjected to evaluation of stain and image preservability to find that the excellent results were obtained similarly to Sample No. 8 of Example 1.
Similarly, Sample No. 201 of Example 2 was processed in the bleaching solution prepared by adding Compound II-1 (0.3 mole/liter) to the bleaching solution of Example 4. The process sample was subjected to evaluation of stain and image preservability to find that the excellent results were obtained similarly to Sample No. 16 of Example 2.
EXAMPLE 6
Layers having the following compositions were provided on a 127 .mu.m thick cellulose triacetate film support having thereon a subbing layer to thereby prepare a multi-layered color light-sensitive material Sample No. 501. The addition amounts are in terms of g/m.sup.2. The amount of colloidal silver and silver halides are the amounts converted to silver.
______________________________________First layer: an anti-halation layerBlack colloidal silver 0.25Gelatin 1.9UV absorber U-1 0.04UV absorber U-2 0.1UV absorber U-3 0.1UV absorber U-4 0.1UV absorber U-6 0.1High-boiling organic solvent Oil-1 0.1Second layer: an intermediate layerGelatin 0.40Compound Cpd-D 10 mgHigh-boiling organic solvent Oil-3 0.1Dye D-4 0.4 mgThird layer: an intermediate layerSilver iodobromide fine grains whose surface 0.05and inside were fogged (average grain size:0.06 .mu.m, a fluctuation coefficient: 18%,AgI content: 1 mole %)Gelatin 0.4Fourth layer: a low red-sensitive layerEmulsion A 0.2Emulsion B 0.3Gelatin 0.8Coupler C-1 0.15Coupler C-2 0.05Coupler C-9 0.05Compound Cpd-D 10 mgHigh-boiling organic solvent Oil-2 0.1Fifth layer: a medium red-sensitive layerEmulsion B 0.2Emulsion C 0.3Gelatin 0.8Coupler C-1 0.2coupler C-2 0.05Coupler C-3 0.2High-boiling organic solvent Oil 2 0.1Sixth layer: a high red-sensitive layerEmulsion D 0.4Gelatin 1.1Coupler C-1 0.3Coupler C-3 0.7Additive P-1 0.1Seventh layer: an intermediate layerGelatin 0.6Additive M-1 0.3Anti-stain agent Cpd-K 2.6 mgUV absorber U-1 0.1UV absorber U-6 0.1Dye D-1 0.02Eighth layer: an intermediate layerSilver iodobromide fine grains whose surface 0.02and inside were fogged (average grain size:0.06 .mu.m, a fluctuation coefficient:16%, AgI content: 0.3 mole %)Gelatin 1.0Additive P-1 0.2Anti-stain agent CpD-J 0.1Anti-stain agent Cpd-A 0.1Ninth layer: a low green-sensitive layerEmulsion E 0.3Emulsion F 0.1Emulsion G 0.1Gelatin 0.5Coupler C-7 0.05Coupler C-8 0.20Compound Cpd-B 0.02Compound Cpd-D 10 mgCompound Cpd-E 0.02Compound Cpd-F 0.02Compound Cpd-G 0.02Compound Cpd-H 0.02High-boiling organic solvent Oil-1 0.1High-boiling organic solvent Oil-2 0.1Tenth layer: a medium green-sensitive layerEmulsion G 0.3Emulsion H 0.1Gelatin 0.6Coupler C-7 0.2Coupler C-8 0.1Compound Cpd-B 0.03Compound Cpd-E 0.02Compound Cpd-F 0.02Compound Cpd-G 0.05Compound Cpd-H 0.05High-boiling organic solvent Oil-2 0.1Eleventh layer: a high green-sensitive layerEmulsion I 0.5Gelatin 1.0Coupler C-4 0.3Coupler C-8 0.1Compound Cpd-B 0.08Compound Cpd-E 0.02Compound Cpd-F 0.02Compound Cpd-G 0.02Compound Cpd-H 0.02High-boiling organic solvent Oil-1 0.02High-boiling organic solvent Oil-2 0.02Twelfth layer: an intermediate layerGelatin 0.6Dye D-1 0.1Dye D-2 0.05Dye D-3 0.07Thirteenth layer: a yellow filter layerYellow colloidal silver 0.1Gelatin 1.1Anti-stain agent Cpd-A 0.01High-boiling organic solvent Oil-1 0.01Fourteenth layer: an intermediate layerGelatin 0.6Fifteenth layer: a low blue-sensitive layerEmulsion J 0.4Emulsion K 0.1Emulsion L 0.1Gelatin 0.8Coupler C-5 0.6Sixteenth layer: a medium blue-sensitive layerEmulsion L 0.1Emulsion M 0.4Gelatin 0.9Coupler C-5 0.3Coupler C-6 0.3Seventeenth layer: a high blue-sensitive layerEmulsion N 0.4Gelatin 1.2Coupler C-6 0.7Eighteenth layer: the first protective layerGelatin 0.7UV absorber U-1 0.04UV absorber U-2 0.01UV absorber U-3 0.03UV absorber U-4 0.03UV absorber U-5 0.05UV absorber U-6 0.05High-boiling organic solvent Oil-1 0.02Formaldehyde scavengerCpd-C 0.2Cpd-I 0.4Dye D-3 0.05Nineteenth layer: the second protective layerColloidal silver 0.1 mgSilver iodobromide fine grains (average grain 0.1size: 0.06 .mu.m, AgI content: 1 mole %)Gelatin 0.4Twentieth layer: the third protective layerGelatin 0.4Polymethyl methacrylate 0.1(average grain size: 1.5 .mu.m)Copolymer of methyl methacrylate and acrylic acid 0.1(4:6) (average grain size: 1.5 .mu.m)Silicone oil 0.03Surfactant W-1 3.0 mgSurfactant W-2 0.03______________________________________
In addition to the above components, additives F-1 to F-8 were added to all the layers. Further, a gelatin hardener H-1 and surfactants W-3 and W-4 for coating and emulsifying besides the above components were added to each layer.
Further, phenol, 1,2-benzisothiazline-3-one, 2-phenoxyethanol, phenethyl alcohol, and p-hydroxybenzoate butyl ester were added as a fungicide and an anti-mold agent.
The characteristics of silver iodobromide emulsions used in the above examples are shown below:
______________________________________ Average Fluctuation AgI grain size coefficient contentEmulsion (.mu.m) (%) (%)______________________________________A, monodispersed tetra- 0.25 16 3.7 decahedral grainsB, monodispersed cubic, 0.30 10 3.3 internal latent image type grainsC, monodispersed tetra- 0.30 18 5.0 decahedral grainsD, polydispersed twinned 0.60 25 2.0 grainsE, monodispersed cubic 0.17 17 4.0 grainsF, monodispersed cubic 0.20 16 4.0 grainsG, monodispersed cubic, 0.25 11 3.5 internal latent image type grainsH, monodispersed cubic, 0.30 9 3.5 internal latent image type grainsI, polydispersed tabular 0.80 28 1.5 grains (average aspect ratio: 4.0)J, monodispersed tetra- 0.30 18 4.0 decahedral grainsK, monodispersed tetra- 0.37 17 4.0 decahedral grainsL, monodispersed cubic, 0.46 14 3.5 internal latent image type grainsM, monodispersed cubic 0.55 13 4.0 grainsN, polydispersed tabular 1.00 33 1.3 grains (average aspect ratio: 7.0)______________________________________Spectral sensitization of Emulsions A to N Added amount Sensitizing per mol of AgX Timing to addEmulsion dye added (g) sensitizing dye______________________________________A S-1 0.025 IV S-2 0.25 IVB S-1 0.01 II S-2 0.25 IIC S-1 0.02 IV S-2 0.25 IVD S-1 0.01 IV S-2 0.10 IV S-7 0.01 IVE S-3 0.5 IV S-4 0.1 IVF S-3 0.3 IV S-4 0.1 IVG S-3 0.25 II S-4 0.08 IIH S-3 0.2 I S-4 0.06 II S-3 0.3 III S-4 0.07 III S-8 0.1 IIIJ S-6 0.2 I S-5 0.05 IK S-6 0.2 I S-5 0.05 IL S-6 0.22 II S-5 0.06 IIM S-6 0.15 IV S-5 0.04 IVN S-6 0.22 II S-5 0.06 II______________________________________ I: during grain formation II: immediately after finishing grain formation III: immediately before starting chemical sensitization IV: immediately after finishing the chemical sensitization ##STR22##
The above Sample No. 501 was subjected to an imagewise exposure and then to processing with a cine type automatic developing machine according to the following processing steps. A half of the sample was first processed with Bleaching Solution 1 and then with the respective stabilizing solutions. The same procedure was repeated to the other half of the sample with Bleaching Solution 2. The samples thus processed were evaluated in the same manner as in Example 1.
______________________________________Processing steps Replenishing Tank Time Temperature Amount CapacityStep (minute) (.degree.C.) (ml) (l)______________________________________Black/white 6 38 1.5 12developing1st Washing 1 38 7.5 4Reversal 1 38 1.1 4Color 4 38 2.0 12developingConditioning 2 38 1.1 4Bleaching 4 38 1.3 12Fixing 3 38 1.3 122nd Washing 1 38 -- 4(1)2nd Washing 1 38 7.5 4(2)Stabilizing 1 38 1.1 4Drying 2 50______________________________________
Replenishing amount: per m.sup.2 of the light-sensitive material
The overflowed solution of the second washing bath (2) was introduced into the second washing bath (1).
The compositions of the respective processing solutions are shown below. The unit is grain unless otherwise described.
______________________________________ Start ReplenishingBlack/white developing solution Soln. Soln.______________________________________Pentasodium nitrilo-N,N,N- 2.0 2.0trimethylenephosphonatePentasodium diethylenetriamine 3.0 3.0pentaacetatePotassium sulfite 30 30Hydroquinone potassium monosulfonate 20 20Potassium carbonate 33 331-Phenyl-4-methyl-4-hydroxymethyl- 2.0 2.03-pyrazolidonePotassium bromide 2.5 0.9Potassium thiocyanate 1.2 1.2Potassium iodine 2.0 mg 2.0 mgWater was added to make 1.0 l 1.0 lpH (25.degree. C.) 9.60 9.70______________________________________
The pH was adjusted with hydrochloric acid or potassium hydroxide.
______________________________________ Start Soln./Replenish-Reversal solution ing Solution Common______________________________________Pentasodium nitrilo-N,N,N-tri- 2.0methylenephosphonateStannous chloride dihydrate 1.0p-Aminophenol 0.1Sodium hydroxide 8.0Glacial acetic acid 15 mlAmmonium sulfite 20Water was added to make 1.0 lpH (25.degree. C.) 6.60______________________________________
The pH was adjusted with acetic acid or aqueous ammonia.
______________________________________ Start Replenish-Color Developing Solution soln. ing soln.______________________________________Pentasodium nitrilo-N,N,N- 2.0 2.0trimethylenephosphonatePentasodium 2.0 2.0diethylenetriaminepentaacetateSodium sulfite 7.0 7.0Tripotassium phosphate 12 hydrate 36 36Potassium bromide 1.0 --Potassium iodide 90 mg --Sodium hydroxide 3.0 3.0Citrazinic acid 1.5 1.5N-ethyl-(.beta.-methanesulfonamidethyl)- 10.5 10.53-methyl-4-aminoanline sulfate3,6-Dithiaoctane-1,8-diol 3.5 45Water was added to make 1.0 l 1.0 lpH (25.degree. C.) 11.90 12.05______________________________________
The pH was adjusted with hydrochloric acid or potassium hydroxide.
______________________________________ Start Soln./Replenish-Conditioning Solution ing Solution Common______________________________________Disodium ethylenediamine 8.0tetraacetate dihydrateSodium sulfite 122-Mercapto-1,3,4-triazole 0.5pH (25.degree. C.) 6.00______________________________________
The pH was adjusted with hydrochloric acid or sodium hydroxide.
______________________________________ Start Soln./Replenish-Bleaching Solution 1 ing Solution Common______________________________________Ethylenediaminetetraacetic acid 3Ferric ammonium ethylenediamine- 150tetraacetate dihydrate2-Mercapto-1,3,4-triazole 0.5Ammonium bromide 120Ammonium nitrate 25Water was added to make 1.0 lpH (25.degree. C.) 4.20______________________________________
The pH was adjusted with acetic acid or aqueous ammonia.
______________________________________ Start Soln./Replenish-Bleaching Solution 2 ing Solution Common______________________________________1,3-Diaminopropanetetraacetic 3acidFerric ammonium 1,3-diamino- 120propanetetraacetic acid dihydrateGlycolic acid 40Acetic acid 30Ammonium bromide 120Ammonium nitrate 25Water was added to make 1.0 lpH (25.degree. C.) 4.20______________________________________
The pH was adjusted with acetic acid or aqueous ammonia.
______________________________________ Start Soln./Replenish-Fixing Solution ing Solution Common______________________________________Disodium ethylenediaminetetraacetate 1.7dihydrateSodium benzoaldehyde-o-sulfonate 20Sodium bisulfite 15Ammonium thiosulfate (700 g/l) 250 mlWater was added to make 1.0 lpH (25.degree. C.) 6.00______________________________________
The pH was adjusted with acetic acid or aqueous ammonia.
Stabilizing Solution
The respective stabilizing solutions used in Example 1 or 2 were used (a start solution/a replenishing solution common).
The image preservability was evaluated on the grey-developed portions of the respective processed samples, in which the magenta densities were 0.5.
The results were similar to those in Examples 1 and 2, that is, excellent results were obtained with the stabilizing solutions containing the N-methylol compounds of the present invention.
Further, the samples were processed according to the above processing procedure, in which were used a stabilizing solution containing no image stabilizer and a conditioning solution containing each 0.03 mole/l of the image stabilizers shown in Table C. The respective samples thus processed were subjected to an evaluation of image preservability as well as the above. The results are shown in Table C.
TABLE C______________________________________ Image preservability* Bleaching BleachingSample No. Image stabilizer Solution 1 Solution 2______________________________________ 1 (Comp.) -- 0.20 0.20 2 (Comp.) Formaldehyde 0 0 3 (Inv.) Compound I-1 0.01 0 4 (Inv.) Compound I-2 0.02 0.01 5 (Inv.) Compound I-3 0.02 0.01 6 (Inv.) Compound I-4 0.02 0.01 7 (Inv.) Compound I-5 0.02 0.01 8 (Inv.) Compound I-26 0.02 0.01 9 (Inv.) Compound I-27 0.02 0.0110 (Inv.) Compound II-1 0.03 0.0211 (Inv.) Compound II-2 0.05 0.0412 (Inv.) Compound II-5 0.03 0.0213 (Inv.) Compound II-7 0.04 0.0414 (Inv.) Compound II-12 0.03 0.02______________________________________ *M fading
As can be found from the results shown in Table C, the application of the N-methylol compounds of the present invention to the conditioning bath can also provide sufficient anti-fading effect for a magenta dye. The excellent results were obtained especially when a ferric complex salt of 1,3-diaminopropanetetraacetic acid was used.
The surfaces of the respective samples in Table C were observed only to find that no stains were observed thereon.
EXAMPLE 7
Sample No. 201 in Example 2 of JP-A-2-90151 and the light-sensitive material 1 in Example i and the light-sensitive material 9 in Example 3 of JP-A-2-93641, each of which was used as a light-sensitive material, was subjected to processing Nos. 8 and 16 of Example 1 above. The results showed that the formaldehyde vapor concentration decreased while an excellent anti-fading effect to a dye image was demonstrated and no stains were observed on the light-sensitive material.
While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.

Number	Date	Country
2-400906	Dec 1990	JPX
3-38969	Feb 1991	JPX
3-38995	Feb 1991	JPX

Number	Name	Date
2487446	Kellog	Nov 1949
2487569	Mackey	Nov 1949
2579435	Mackey	Dec 1951
2579436	Mackey	Dec 1951
3801322	Shirasu et al.	Apr 1974
4786583	Schwartz	Nov 1988
4859574	Gormel	Aug 1989
4975356	Cullinan	Dec 1990
5188925	Hagiwara et al.	Feb 1993

Number	Date	Country
2153348	Jun 1990	JPX
908136	Oct 1962	GBX
1392134	Feb 1973	GBX

Color image-stabilization processing solution used for processing a silver halide color photographic material and a processing method using the same

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