Method of bleaching silver halide color photographic light-sensitive materials using particular ferric chelates

FIELD OF THE INVENTION
The present invention relates to a method for processing silver halide color photographic light-sensitive materials. More specifically, the present invention relates to a method for processing silver halide color photographic light-sensitive materials, which uses a processing solution high in biodegradability and is capable of minimizing the amount of waste liquids and providing images lower in bleach fogging.
BACKGROUND OF THE INVENTION
In general, silver halide color photographic light-sensitive materials are processed by use of a color developer, a bleach, a fixer, a bleach-fixer and a stabilizer. Among these processing solutions, the bleach and bleach-fixer contain a bleaching agent to bleach silver. For this purpose, ethylenediaminetetraacetate ferric complex salts are most widely used at present in processing color paper and color negative films. However, ethylenediaminetetracetate ferric complex salts are poor in biodegradability. If accidently discharged into a river or soil, they are accumulated there for a long time without undergoing degradation and, thereby, pollute the natural environment. Recently, 1,3-propanediaminetetracetate ferric complex salts (PDTA-Fe) described, for example, in Japanese Pat. O.P.I. Pub. Nos. 103041/1990, 103040/1990, 250651/1988 have been used. Although PDTA-Fe has high bleaching power and excellent rapid-processing capability, it causes bleach fogs when bleaching is carried out immediately after color developing. To eliminate the problem, the pH can be lowered by use of acetic acid or the like, but it causes other problems such as offensive smell and higher biochemical oxygen demand.
Another disadvantage of PDTA-Fe is its strong oxidizing power; therefore, thiosulfates used as fixing agent are decomposed into sulfur or sulfides when bleaching with PDTA-Fe is followed by processing with a fixer, or when PDTA-Fe is used as bleaching agent in a bleach-fixer.
Though diethylenetriaminepentaacetate ferric complex salts described, for example, in Japanese Pat. O.P.I. Pub. Nos. 118752/1986, 50145/1986, 50150/1986, 50147/1986 are known as a third bleaching agent, they also have shortcomings.
That is, these are not only poor in biodegradability but also are liable to cause yellow stains on edges of a light-sensitive material when used in processing color paper, particularly in processing carried out at a low replenishing rate.
Bleaching agents described, for example, in EPO, 430,000A1 and German Pat. No. 3,939,756 are known as compounds having high biodegradability, but these bleaching agents are apt to lower the desilverizing property when employed in processing at a low replenishing rate and, as a result, deteriorate the rapid processing capability.
Methods for regenerating a bleach-fixer are described, for example, in Japanese Pat. O.P.I. Pub. Nos. 48245/1991 and 121451/1991. These methods, however, are used for regenerating bleach-fixers by means of a ferric complex salt of an aminopolycarboxylic acid such as ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, cyclohexanediaminetetraacetic acid or 1,3-diaminopropanetetraacetic acid. These compounds have a disadvantage of poor biodegradability or a tendency to decompose a fixing agent as described above. Therefore, these methods give neither suggestion as to the compound of the invention nor hint as to the effect of the invention described below.
SUMMARY OF THE INVENTION
Accordingly, a first object of the invention is to provide a method for processing a silver halide color photographic light-sensitive material, which uses a bleach or bleach-fixer excellent in biodegradability and environmental compatibility; a second object of the invention is to provide a method for processing a silver halide color photographic light-sensitive material, which can minimize the amount of waste liquids, reduce running cost and improve environmental compatibility; a third object of the invention is to provide a method for processing a silver halide color photographic light-sensitive material, which causes fewer yellow stains on edges of a light-sensitive material and less bleach fogging; and a fourth object of the invention is to provide a method for processing a silver halide color photographic light-sensitive material, which can provide a stable photographic processing capability over a long period.
The above objects of the invention are attained by a method for processing a light-sensitive material which comprises, after color development, processing of a light-sensitive material with a processing solution having a bleaching capability, wherein a used processing solution having a bleaching capability is regenerated by addition of a regenerant, and the bleaching agent contained in the processing solution having a bleaching capability is a ferric complex salt of a compound represented by the following formula [A-I], [A-II] or [A-III]: ##STR2##
In the formula, A.sub.1, A.sub.2, A.sub.3 and A.sub.4, which may be the same or different, each represent a hydrogen atom, an hydroxyl, --COOM, --PO.sub.3 (M).sub.2, --CH.sub.2 COOM, --CH.sub.2 OH or lower alkyl group, provided that at least one of A.sub.1, A.sub.2, A.sub.3 and A.sub.4 is a --CH.sub.2 COOM, --COOM or --PO.sub.3 (M).sub.2 group; M, M.sub.1 and M.sub.2 each represent a hydrogen atom, an ammonium group, a sodium, potassium or lithium atom or an organic ammonium group. ##STR3##
In the formula, A.sub.1, A.sub.2, A.sub.3 and A.sub.4 each represent a --CH.sub.2 OH, --PO.sub.3 (M).sub.2 or --COOM group and may be the same or different; M represents a hydrogen atom or alkali metal atom or an ammonium or organic ammonium group; X represents an alkylene group having 2 to 6 carbon atoms or a --(B.sub.1 O).sub.n --B.sub.2 -- group, where n represents an integer of 1 to 8, B.sub.1 and B.sub.2, which may be the same or different, each represent an alkylene group having 1 to 5 carbon atoms. ##STR4##
In the formula, A.sub.1, A.sub.2, A.sub.3 and A.sub.4 each represent a --CH.sub.2 OH, --PO.sub.3 (M.sub.2).sub.2 or --COOM.sub.1 group and may be the same or different, where M.sub.1 and M.sub.2 each represent a hydrogen atom or alkali metal atom or an ammonium or organic ammonium group; X represents a straight-chain or branched alkylene group having 2 to 6 carbon atoms, a saturated or unsaturated ring-forming organic group or a --(B.sub.1 O)n--B.sub.2 -- group, where n is an integer of 1 to 8, B.sub.1 and B.sub.2, which may be the same or different, each represent an alkylene group having 1 to 5 carbon atoms; n.sub.1, n.sub.2, n.sub.3 and n.sub.4 each represent an integer of 1 or more and may be the same or different, provided that at least one of them is 2 or more.
One preferable embodiment of the invention is the method for processing silver halide color photographic light-sensitive materials in which the processing solution having a bleaching capability is a bleach.
Another preferable embodiment of the invention is the method for processing silver halide color photographic light-sensitive materials in which the amount of ammonium ions contained in the processing solution having bleaching capability is not more than 50 mol % of the total cat ions contained therein.
DETAILED DESCRIPTION OF THE INVENTION
The invention is hereinafter described in detail.
In the invention, the processing solution having a bleaching capability means a bleach or a bleach-fixer.
In Formula [A-I], A.sub.1, A.sub.2, A.sub.3 and A.sub.4, which may be the same or different, each represent a hydrogen atom, a hydroxyl, --COOM, --OP.sub.3 (M).sub.2 or --CH.sub.2 OH group, or a lower alkyl group such as a methyl, ethyl, isopropyl or n-propyl group, provided that at least one of A.sub.1, A.sub.2, A.sub.3 and A.sub.4 is a --COOM or --PO.sub.3 (M).sub.2 group. M, M.sub.1 and M.sub.2 each represent a hydrogen atom, an ammonium group, a sodium, potassium or lithium atom or an organic ammonium group such as a trimethyl ammonium or triethanol ammonium group.
Preferable examples of the compound represented by Formula [A-I] are shown below: ##STR5##
These compounds represented by Formula [A-I] can be synthesized according to the general synthetic methods described, for example, in Japanese Pat. O.P.I. Pub. Nos. 267750/1988, 267751/1988, 115172/1990, 295954/1990. Among these compounds, those denoted by (A-I-1) and (A-I-2) are particularly preferred.
The compound represented by Formula [A-II] is described hereunder.
In the formula, A.sub.1 to A.sub.4, which may be the same or different, each represent a --CH.sub.2 OH, --PO.sub.3 (M).sub.2 or --COOM group, where M is a hydrogen atom, an alkali metal atom such as sodium or potassium or another cation such as ammonium, methyl ammonium or trimethyl ammonium. X represents a substituted or unsubstituted alkylene group or a --(B.sub.1 O)n--B.sub.2 -- group each having 2 to 6 carbon atoms, where B.sub.1 and B.sub.2, which may be the same or different, each represent a substituted or unsubstituted alkylene group having 1 to 5 carbon atoms. Examples of the alkylene group represented by X include an ethylene group, trimethylene group and tetramethylene group. Examples of the alkylene group represented by B.sub.1 and B.sub.2 group include a methylene group, ethylene group and trimethylene group. Examples of the substituent of the alkylene group represented by X, B.sub.1 or B.sub.2 include a hydroxyl group and an alkyl group having 1 to 3 carbon atoms such as a methyl and ethyl group. n represents an integer of 1 to 8, preferably 1 to 4. Preferable examples of the compound represented by Formula [A-II] are shown below but the scope of the invention is not limited to them. ##STR6##
The compounds represented by Formula [A-II] can be synthesized according to a conventional method.
Among these compounds, those denoted by (A-II-1), (A-II-3) and (A-II-14) are particularly preferred.
The compounds represented by Formula [A-III] are described hereunder.
In the formula, A.sub.1 to A.sub.4, which may be the same or different, each represent a --CH.sub.2 OH, --PO.sub.3 (M.sub.2).sub.2 or --COOM.sub.1 group, where M.sub.1 and M.sub.2 each represent a hydrogen ion, an alkali metal ion such as a sodium or potassium ion, or another cation such as an ammonium, methyl ammonium or trimethyl ammonium ion.
X represents a straight-chain or branched alkylene group having 2 to 6 carbon atoms, a ring-forming saturated or unsaturated organic group or a --(B.sub.1 O).sub.n B.sub.2 -- group, where B.sub.1 and B.sub.2, which may be the same or different, each represents an alkylene group having 1 to 5 carbon atoms (including those having a substituent). n.sub.1 to n.sub.4, which may be the same or different, each represent an integer of 1 or more, provided that at least one of them is 2 or more. Examples of the alkylene group represented by X include an ethylene, trimethylene and tetramethylene group. Examples of the alkylene group represented by B.sub.1 or B.sub.2 include a methylene group, ethylene group and trimethylene group. Examples of the substituent of the alkylene group represented by X, B.sub.1 or B.sub.2 include a hydroxyl group and an alkyl group having 1 to 3 carbon atoms such as a methyl and ethyl group. n represents an integer of 1 to 8, preferable 1 to 4 and especially 1 to 2. The following are preferable examples of the compound represented by Formula [A-III], but preferable ones are not limited to them. ##STR7##
Among the above compounds, those denoted by (A-III-16), (A-III-17), (A-III-18), (A-III-19) and (A-III-20) contain both transforms and cis forms.
The compounds represented by Formula [A-III] can be synthesized by the usual method.
Among preferable examples, the compounds denoted by (A-III-1), (A-III-2) and (A-III-6) are particularly preferred.
The addition amount of a ferric complex salt of the compound represented by Formula [A-I], [A-II] or [A-III] is preferably within the range of 0.1 to 2.0 mole, especially within the range of 0.1 to 1.5 mole per liter of bleach or bleach-fixer.
In the invention, ferric complex salts of the following compounds can also be used as bleaching agents besides the ferric complex salts of the compound represented by Formula
[A-I], [A-II] or [A-III].
[A'-I] Ethylenediaminetetraacetic acid
[A'-2] Trans-1,2-cyclohexanediaminetetraacetic acid
[A'-3] Dihydroxyethylglycin
[A'-4] Ethlenediamine-tetrakismethylene-phosphonic acid
[A'-5] Nitrilotrismethylene-phosphonic acid
[A'-6] Diethylenetriamine-pentakismethylene-phosphonic acid
[A'-7] Diethylenetriaminepentaacetic acid
[A'-8] Ethylenediamine-di-ortho-hydroxyphenylacetic acid
[A'-9] Hydroxyethyl-ethylenediaminetriacetic acid
[A'-10] Ethylenediaminepropionic acid
[A'-11] Ethylenediaminediacetic acid
[A'-12] Hydroxyethyliminodiacetic acid
[A'-13] Nitrilotriacetic acid
[A'-14] Nitrilotripropionic acid
[A'-15] Triethylenetetraminehexacetic acid
[A'-16] Ethylenediaminetetrapropionic acid
[A'-17] 1,3-Propylenediaminetetraacetic acid
[A'-18] Glycol-ether-diaminetetraacetic acid
In one preferable embodiment of the invention, exemplified compounds (I-1) to (VII-20) on pages 79-142 of the specification of Japanese Pat. Appl. No. 256383/1985 are added to the bleaching-capable processing solution of the invention. Among these compounds, particularly preferred ones are those denoted by (B-1) to (B-30) below. ##STR8##
These compounds are used in an amount of preferably 0.05 to 50 g, especially 0.1 to 20 g per liter of processing solution.
Among these processing solutions having a bleaching capability, particularly preferred are a bleach using a ferric complex salt of the compound of Formula [A-I] and a bleach-fixer using a ferric complex salt of the compound of Formula [A-II].
These bleaches and bleach-fixers are used in a temperature range of 20.degree. to 50.degree. C., preferably 25.degree. to 45.degree. C.
The pH of the bleach is preferably not more than, especially 1.0 to 5.5. The pH of the bleach-fixer is preferably 5.0 to 9.0, especially 6.0 to 8.5. The pH of the bleach or the bleach-fixer described here is a pH of a processing bath in which a silver halide light-sensitive material is being processed, and it is clearly distinguished from the pH of a replenisher.
In addition to the above compounds, the bleach or the bleach-fixer may contain halides, such as ammonium bromide and sodium bromide, as well as a variety of optical whitening agents, defoamers and surfactants.
A preferred replenishing amount of the bleach or the bleach-fixer is not more than 1000 ml, preferably 20 to 600 ml and especially 40 to 500 ml per square meter of light-sensitive material. As the replenishing amount decreases, the effect of the invention becomes more conspicuous.
In the invention, air or oxygen may be blown into a processing bath and a replenisher storage tank, if desired, in order to raise the activity of the bleach or the bleach-fixer. Addition of a suitable oxidizing agent, such as hydrogen peroxide, bromates or persulfates, is also effective as an alternative measure.
As fixing agent used in the fixer or the bleach-fixer according to the invention, thiocyanates or thiosulfates are preferably used. The thiocyanate content is at least 0.1 mol/l and, in processing color negative films, it is preferably not less than 0.5 mol/l, especially not less than 1.0 mol/l. The content thiosulfate content is at least 0.2 mol/l and, in processing color negative films, it is preferably not less than 0.5 mol/l.
The objects of the invention are attained much more effectively by using jointly thiocyanates and thiosulfates.
Besides these fixing agents, the bleach or the bleach-fixer of the invention may contain one or more types of pH buffers comprising various salts. Further, it is preferred that rehalogenating agents, such as alkali halides and ammonium halides including potassium bromide, sodium bromide, sodium chloride and ammonium bromide, be contained therein in a large amount.
There may also be added alkylamines and polyethylene oxides which are usually known as additives for a fixer or a bleach-fixer.
Silver may be recovered from the bleach-fixer of the invention according to the usual method.
The processing time with the bleach and the fixer is not limited, but it is desirably not more than 3 min and 30 sec, more desirably within the range of 10 sec to 2 min and 20 sec, and most desirably within the range of 20 sec to 1 min and 20 sec. The processing time with the bleach-fixer is preferably not more than 4 min, especially within the range of 10 sec to 2 min and 20 sec.
In the embodiment of the invention, the effect of the invention can be brought out well when the content of ammonium ions in the bleach, or in the bleach-fixer and the regenerant described later, is not more than 50 mol % of the total amount of cations contained therein. Preferably, the amount is not more than 30 mol %; in a particularly preferred embodiment, it is not more than 10 mol %.
In order to bring out the effect of the invention adequately and to improve the rapid processing capability, it is preferable that the bleach or the bleach-fixer used in the invention be subjected to forced stirring. The term "forced stirring" used here does not mean ordinary self-stirring due to flow of a liquid, but it means to stir the processing solution forcedly by use of a stirring means. Usable stirring means include those described in Japanese Pat. O.P.I. Pub. Nos. 222259/1989 and 206343/1989.
As another effect of the invention, bleach fogging can be minimized by setting the crossover time from a color developing bath to a bleaching or bleach-fixing bath at not more than 10 seconds, preferably not more than 7 seconds.
In view of the effect of the invention, it is preferable not to use acetic acid in the bleach and the bleach-fixer of the invention.
Further, it is preferable that the bleach and the bleach-fixer of the invention contain a compound represented by the following formula [II]:
A(--COOM)n Formula [II]
In the formula, A is an n-valent organic group, n is an integer of 1 to 6 and M represents an ammonium, an alkali metal atom (sodium, potassium, lithium) or a hydrogen atom.
In Formula [II], the n-valent organic group represented by A includes an alkylene group (e.g., methylene, ethylene, trimethylene, tetramethylene), an alkenylene group (e.g., ethenylene), an alkynylene group (e.g., ethynylene), a cycloalkylene group (e.g., 1,4-cyclohexanediyl), an arylene group (e.g., o-phenylene, p-phenylene), an alkanetriyl group (e.g., 1,2,3-propanetriyl) and an arenetriyl group (e.g., 1,2,4-benzenetriyl).
The n-valent group represented by A includes those having a substituent such as a hydroxyl or alkyl group or a halogen atom: examples thereof include 1,2-dihydroxyethylene, hydroxyethylene, 2-hydroxy-1,2,3-propanetriyl, methyl-p-phenylene, 1-hydroxy-2-chloroethylene, chloromethylene and chloroethenylene.
The following are typical examples of the compound represented by Formula [II]: ##STR9##
Among the above exemplified compounds, preferred ones are those denoted by [II-1], [II-3], [II-4], [II-5], [II-16], [II-18], [II-23]; the particularly preferred one is that denoted by [II-5].
The compound represented by Formula [II] is used in an amount of preferably 0.05 to 2 mol, especially 0.2 to 1.0 mol per liter of processing solution.
In the invention, a used bleach or bleach-fixer is regenerated by addition of a regenerant and reused as a regenerated bleach or bleach-fixer. Components (e.g., silver ions) accumulated in a used processing solution may be removed or decreased by the usual methods such as the steel wool method disclosed in Japanese Pat. O.P.I. Pub. No. 3624/1973, U.S. Pat. No. 4,065,313, the electrolytic method disclosed in U.S. Pat. Nos. 4,014,764, 4,036,715, Japanese Pat. Exam. Pub. No. 40490/1978, Japanese Pat. O.P.I. Pub. No. 232452/1986, and the dilution method disclosed in Japanese Pat. Exam. Pub. No. 33679/1981. Or a used processing solution may be reused as a regenerated replenisher after it is regenerated by merely adding a regenerant, without being subjected to the above removal treatment. For the bleach-fixer, it is preferable to remove silver when recovery of silver is important; or it is preferable to reuse a regenerated bleach(-fixer) or replenisher by only adding a regenerant without desilverization when simplicity of processing is the first consideration.
As a rule, the regenerant is added to an overflown liquid to compensate for the components lost in the bleach-fixing process.
Preferably, the regenerant used in the invention comprises the same bleaching agent, fixing agent and preservative as those used in the bleach or the bleach-fixer and, if necessary, a bleach accelerator, a rehalogenating agent, a pH buffer and a small amount of an acid.
When the bleach or bleach-fixer is used without taking such a removal means, influence is liable to occur due to the accumulation of developer components brought from the preceding developing bath. In the invention, though such an unwanted influence could be reduced beyond expectation, it is preferable to add a small amount of an acid to the overflown liquid to further minimise such an unwanted influence.
As acid contained in the regenerant, any organic or inorganic acid can be used, but hydrochloric acid, nitric acid and acetic acid are particularly preferred in obtaining adequate effects of the invention. The addition amount thereof is usually 1 to 30 grams per liter of regenerated replenisher; preferably, these acids are used in an amount necessary to adjust the pH of a regenerated replenisher to 4.0 to 6.0.
For the same reason, the amount of the bleaching agent used as a regenerant component is usually 0.1 to 50 grams, preferably 1 to 50 grams per liter of regenerated replenisher or overflown liquid.
In practice, a used bleach or bleach-fixer (overflow) is collected in a tank, and when it reaches a certain volume, the regenerant is added thereto to make it a replenisher. The overflow can be recycled any number of times, and if necessary, it may be subjected to the above treatment for removing accumulated components after repeating a prescribed number of regenerations.
The color photographic light-sensitive material, to which the processing method of the invention is applied, is described hereunder.
The light-sensitive material suitable for the method of the invention includes those used as color negative films, color paper and color reversal films. And, in the embodiment of the invention, desirable color negative films are those comprising silver iodobromide grains having an average silver iodide content of 3 mol %; a more desirable average silver iodide content is 4 to 15 mol %; an even more desirable silver iodide content is 5 to 12 mol %; and the most desirable average silver iodide content is 8 to 11 mol %.
The light-sensitive material for color negative films used in the invention may employ the silver halide emulsions described in Research Disclosure No. 308119 (hereinafter abbreviated as RD308119). Locations of relevant descriptions are shown below.
______________________________________[Item] [Page of RD308119]______________________________________Iodide structure 993 Sec. I-APreparation process 933 Sec. I-A and 994 Sec. ECrystal habit Regular 993 Sec. I-AcrystalTwin crystal 993 Sec. I-AEpitaxial 993 Sec. I-AHalogen composition 993 Sec. I-B(Uniform)Halogen composition (Not 993 Sec. I-BuniformHalogen conversion 994 Sec. I-CHalogen replacement 994 Sec. I-CMetals contained 994 Sec. I-DMonodispersion 995 Sec. I-FSolvent addition 995 Sec. I-FLatent image forming 995 Sec. I-Gposition (Surface)Latent image forming 995 Sec. I-Gposition (Inside)Light-sensitive material 995 Sec. I-HNegativeLight-sensitive material 995 Sec. I-HPositive (containinginternally fogged grains)Use of emulsions as a 995 Sec. I-JmixtureDesalting 995 Sec. II-A______________________________________
In the invention, silver halide emulsions are subjected to physical ripening, chemical ripening and spectral sensitization and then used. In these processes, there can be used the additives described in Research Disclosure Nos. 17643, 18716 and 308119 (hereinafter abbreviated as RD17643, RD18716 and RD308119, respectively).
Locations of relevant descriptions are as follows:
______________________________________[Item] [Page of RD308119] [RD17643] [RD18716]______________________________________Chemical 996 Sec. III-A 23 648sensitizerSpectral 996 Sec. IV- 23-24 648-9sensitizer A,B,C,D,E,H,I,JSupersensitizer 996 Sec. IV-A-E,J 23-24 648-9Antifoggant 998 VI 24-25 649Stabilizer 998 VI 24-25 649______________________________________
Conventional photographic additives usable in the invention are also described in the above Research Disclosures. Locations of relevant descriptions are as follows:
______________________________________[Item] [Page of RD308119] [RD17643] [RD18716]______________________________________Anti-color-mixing 1002 Sec. VIII-I 25 650agentDye image 1001 Sec. VII-J 25 --stabilizerWhitening agent 998 V 24 --UV absorbent 1003 Sec. VIII-C 25-26 -- Sec. XIII-CLight absorbent 1003 VIII 25-26 --Light scattering 1003 VIII -- --agentFilter dye 1003 VIII 25-26 --Binder 1003 IX 26 651Antistatic agent 1006 XIII 27 650Hardener 1004 X 26 651Plasticizer 1006 XII 27 650Lubricant 1006 XII 27 650Surfactant, 1005 XI 26-27 650coating aidMatting agent 1007 XVI -- --Developer (contained in 1011 Sec. XX-B light-sensitive material)______________________________________
Various couplers can be used in the light-sensitive material usable in the invention. Typical examples of such couplers are also described in the above Research Disclosures. Locations of relevant descriptions are as follows:
______________________________________ [RD17643][Item] [Page of RD308119] [RD18716]______________________________________Yellow coupler 1001 Sec. VII-D Sec. VII-C-GMagenta coupler 1001 Sec. VII-D Sec. VII-C-GCyan coupler 1001 Sec. VII-D Sec. VII-C-GDIR coupler 1001 Sec. VII-F Sec. VII-FBAR coupler 1002 Sec. VII-F --Other useful group 1001 Sec. VII-F --releasing couplerAlkali-soluble 1001 Sec. VII-E --coupler______________________________________
The additives used in the invention can be added by the dispersing method or the like described in XIV of RD308119.
The light-sensitive material usable in the invention can employ the supports described on page 28 of RD17643, pages 647-8 of RD18716 and in XIX of RD308119.
In the light-sensitive material usable in the invention, there may be provided auxiliary layers such as a filter layer and an intermediate layer described in Section VII-K in RD308119. Further, the light-sensitive material may have various layer configurations, such as conventional layer order, inverted layer order and unit layer structure described in Section VII-K in RD308119.
The light-sensitive material for color paper processable according to the invention is described hereunder.
As silver halide grains contained in such a light-sensitive material, there are used silver chloride rich silver halide grains containing at least 80 mol % silver chloride. This silver chloride content is desirably not less than 90 mol %, more desirably not less than 95 mol % and most desirably not less than 99 mol %.
The above silver chloride rich silver halide emulsion may contain silver bromide and/or silver iodide as other silver halide compositions. In this case, the amount of silver bromide is desirably not more than 20 mol %, more desirably not more than 10 mol % and most desirably not more than 3 mol %; when silver iodide is contained, its amount is desirably not more than 1 mol %, more desirably not more than 0.5 mol % and most desirably zero. Those silver halide grains which contain 50 mol % or more silver chloride only need to be used in at least one silver halide emulsion layer of the light-sensitive material, but it is preferable that these be used in every light-sensitive silver halide emulsion layer.
These silver halide grains may be regular crystals, twins or other types of crystals and may have an arbitrary [1.0.0] plane to [1.1.1] plane ratio. The crystal structure of these silver halide grains may be uniform from the inner part to the outer part, or it may be a core/shell structure in which the inner part and the outer part form different phases respectively. Further, these silver halide grains may be those which form latent images mostly on the surface or those which form latent images mostly inside of grains. Moreover, there may be used tabular silver halide grains (see Japanese Pat. O.P.I. Pub. Nos. 113934/1983 and Japanese Pat. Appl. No. 170070/1984). Besides the above, the silver halide grains disclosed in Japanese Pat. O.P.I. Pub. Nos. 26837/1989, 26838/1989 and 77047/1989 can also be used.
The silver halide grains may be prepared by any of the acid method, the neutral method and the ammoniacal method.
Further, these may also be prepared through steps of making seed grains firstly by the acid method and then growing them to a prescribed grain size by the ammoniacal method which can provide a larger growth rate. In growing silver halide grains, it is preferable to add, with stirring, silver ions and halide ions simultaneously and sequentially in amounts corresponding to the growth rate of silver halide grains while controlling the pH and pAg of the reaction system, as described in Japanese Pat. O.P.I. Pub. No. 48521/1979.
The light-sensitive material to be processed according to the method of the invention contains couplers in its silver halide emulsion layers.
The red-sensitive layer may contain non-diffusible color couplers to form cyan portion color images; namely, phenol-type or a-naphthol-type couplers in general. The green-sensitive layer may contain at least one non-diffusible color coupler to form magenta portion color images; namely, 5-pyrazolone-type or pyrazolotriazole-type couplers in general. The blue-sensitive layer may contain non-diffusible color couplers to form yellow portion color images; namely, color couplers having an open-chain ketomethylene group. These color couplers may be six-, four- or two-equivalent couplers.
In the invention, two-equivalent couplers are particularly preferred.
Suitable couplers are disclosed, for example, in Farbkuppler by W. Pelz in Mitteilunglnausden Forschungslaboratorien der Agfa, Leverkusen/Munchen, Vol. III, p. 111 (1961); The Chemistry of Synthetic Dyes by K. Venkataraman, Vol. 4, pp. 341-387, Academic Press; The Theory of the Photographic Process, 4th Ed., pp. 353-362; and Research Disclosure No. 17643, Sec. VII.
From a viewpoint of the effect of the invention, preferred color couplers include the magenta couplers represented by Formula [M-1] on page 26 of the specification of Japanese Pat. O.P.I. Pub. No. 106655/1988 (typical examples are those shown on pages 29-34 of the same specification by serial numbers of 1 to 77); the cyan coupler represented by Formula [C-1] or [C-2] on page 34 of the specification {typical examples are those shown on pages 37-42 of the specification by (C'-1) to (C'-82) and (C"-1) to (C"-36)}; and the high-speed yellow coupler described on page 20 of the specification {typical examples are those shown on pages 21-26 of the specification by (Y'-1) to (Y'-39)}.
In order to attain the objects of the invention more effectively, it is preferable to use a magenta coupler represented by the following formula [M-I] in the color light-sensitive material relevant to the invention. ##STR10##
In the magenta coupler having the above formula, Z represents a group of non-metal atoms necessary to form a nitrogen-containing heterocycle, which may have a substituent. X represents a hydrogen atom or a group capable of splitting off upon reaction with an oxidation product of a color developing agent. And R represents a hydrogen atom or a substituent.
In Formula [M-I], the substituent represented by R is not necessarily limited to specified ones, but it is typically an alkyl, aryl, anilino, acylamino, sulfonamido, alkylthio, arylthio, alkenyl or cycloalkyl group. Besides the above, it may also be a halogen atom, a cycloalkenyl, alkynyl, heterocyclic, sulfonyl, sulfinyl, phosphonyl, acyl, carbamoyl, sulfamoyl, cyano, alkoxy, aryloxy, heterocycloxy, siloxy, acyloxy, carbamoyloxy, amino, alkylamino, imido, ureido, sulfamoylamino, alkoxycarbonylamino, aryloxycarbonylamino, alkoxycarbonyl, aryloxycarbonyl or heterocyclothio group, a spiro-compound residue, or a bridged hydrocarbon compound residue.
Preferred ranges and typical examples of the substituent represented by R, those of the group capable of splitting off upon reaction with an oxidation product of a color developing agent, those of the nitrogen-containing heterocycle and those of the substituent which the ring formed by Z may have as well as preferred ranges of the magenta dye represented by Formula [M-I], are the same as those described from the 23rd line of page 5 through the 5th line of page 8 of the specification of No. 0327272.
The following are typical examples of the magenta coupler represented by Formula [M-I]: ##STR11##
Besides the above typical examples, other examples of the compound according to the invention include the compounds of numbers 13, 34, 42, 57-59, 61-62, 65-67 selected from those described on pages 63-82 of the specification of Japanese Pat. Appl. No. 218720/1990; the compounds denoted by numbers 3, 5-20, 22-33, 35-60, 62-77 among those described on pages 10-28 of the specification of No. 0327272; and the compounds denoted by numbers 1-4, 6, 8-17, 19-24, 26-43, 45-59, 61-104, 106-121, 123-162, 164-223 on pages 36-92 of the specification of No. 0235913.
The foregoing couplers can be synthesized according to the methods described in Journal of the Chemical Society, Perkin I (1977), pp. 2047-2052, U.S. Pat. No. 3,725,067, Japanese Pat. O.P.I. Pub. Nos. 99437/1984, 42045/1983, 162548/1984, 171956/1984, 33552/1985, 43659/1985, 172982/1985, 190779/1985, 209457/1987 and 307453/1988.
These couplers can be used, singly or together with other types of magenta couplers, in amounts of 1.times.10.sup.-3 to 1 mole, preferably 1.times.10.sup.-2 to 8.times.10.sup.-1 mole per mole of silver halide.
Addition of a nitrogen-containing heterocyclic mercapto compound to a light-sensitive material using a silver chloride rich emulsion is one preferable embodiment of the invention, because it not only brings out well the effect of the invention, but also effectively mitigates unwanted influences upon photographic properties when a bleach-fixer is mixed into a color developer.
Suitable examples of such nitrogen-containing heterocyclic mercapto compounds include those exemplifided by (I'-1) to (I'-87) on pages 42-45 of the specification of Japanese Pat. O.P.I. Pub. No. 106655/1988.
Silver halide emulsion used in the light-sensitive material relevant to the invention can be prepared by conventional methods (for example, single- or double-Jet injection of materials at a constant or accelerated addition rate). The preferred method comprises double-jet injection of materials at a controlled pAg; see Research Disclosure No. 17643, Secs. I and II.
The silver halide emulsion can be chemically sensitized. Preferred chemical sensitizers are sulfur-containing compounds such as allyl isothiocyanate, allylthiourea and thiosulfates. Reducing agents can also be used as chemical sensitizers; examples thereof include the silver compounds such as those disclosed in Belgian Pat. Nos. 493,464 and 568,687, and polyamines such as diethylenetriamine and aminomethylsulfonic acid derivatives disclosed in Belgian Pat. No. 547,323. Noble metals such as gold, platinum, palladium, iridium, ruthenium and rhodium and compounds thereof are also useful sensitizers for the emulsion. Details of this chemical sensization are described in R. Kosiovsky's article which appeared in Z. Wiss. Photo., Vol. 46, pp. 65-72 (1951), and Research Disclosure No. 17643, Sec. III.
This silver chloride rich emulsion can be spectrally sensitized by conventional methods which use ordinary polymethine dyes such as neutrocyanine, basic or acid carbocyanine, rhodacyanine or hemicyanine, styryl dyes, oxonols or analogues thereof. Details of this spectral sensitization are described in The Cyanine Dyes and Related Compounds by F. M. Hamer, (1964), p. 431, and Research Disclosure No. 17643, Sec. IV.
The silver chloride rich emulsion can use conventional antifoggants and stabilizers. Adeindenes are useful stabilizers; tetra- and penta-adeindene are preferred, and those having a hydroxyl or amino group as substituent are especially preferred. This type of compounds are described in Birr's article in Z. Wiss. Photo., Vol. 47 (1952), pp. 2-58, and Research Disclosure No. 17643, Sec. IV.
The component of the light-sensitive material can be incorporated by the usual method: see U.S. Pat. Nos. 2,322,027, 2,533,514, 3,689,271, 3,764,336 and 3,765,897. Some of the components, such as couplers and UV absorbents, can also be incorporated in the form of charged latices: see German Offenlegungshrift No. 2,541,274 and European Pat. Appl. No. 14,921. Some of the components can be fixed as a polymer in the light-sensitive material: see German Offenlegungshrift No. 2,044,922 and U.S. Pat. Nos. 3,370,952 and 4,080,211.
In the embodiment of the invention, use of a vinylsulfone-type hardener in the light-sensitive material brings out well the effect of the invention.
The vinylsulfone-type hardener is a compound having a vinyl group, or a group capable of forming a vinyl group, bonded with a sulfonyl group; preferred ones are those having at least two vinyl groups, or at least two groups capable of forming vinyl groups, each bonded with a sulfonyl group. Preferred examples thereof are those represented by the following formula [VS-I]:
L--(SO.sub.2 --X)m Formula [VS-I]
In Formula [VS-I], L is a m-valent linking group; X is --CH.dbd.CH.sub.2 or --CH.sub.2 CH.sub.2 Y; Y is a group capable of splitting off in the form of HY due to a salt, for example, a halogen atom, a sulfonyloxy or sulfoxy (including salt) group, or a tertiary amine residue; and m is an integer of 2 to 10; when m is 2 or more, --SO.sub.2 --X's may be the same or different.
The linking group L is an m-valent group formed by combination of an aliphatic hydrocarbon group (e.g., alkylene, alkylidene, alkylidine or a group formed by bonding thereof) or an aromatic hydrocarbon group (e.g., arylene or a group formed by bonding thereof) with one or more of bonds expressed by --O--, --NR'-- (R' is a hydrogen atom, or preferably an alkyl group having 1 to 15 carbon atoms), --S--, --N , --CO--, --SO--, --SO.sub.2 -- or --SO.sub.3 --. When a plurality of (--NR'--)s are contained in a linking group L, these (R')'s may bond with each other to form a ring. Further, the linking group L may have a substituent such as a hydroxy, alkoxy, carbamoyl, sulfamoyl, alkyl or aryl group.
Preferred examples of X are --CH.dbd.CH.sub.2 and --CH.sub.2 CH.sub.2 Cl.
Typical examples of the vinylsulfone-type hardener are shown below. ##STR12##
Other examples of the vinylsulfone-type hardener include those exemplified on pages 122-128 of the specification of Japanese Pat. Appl. No. 274026/1990 by (VS-1), (VS-3), (VS-5), (VS-7), (VS-8), (VS-11), (VS-13) to (VS-21), (VS-23) to (VS-32), (VS-34) to (VS-53) and (VS-55) to (VS-57).
These vinylsulfone-type hardeners according to the invention include the aromatic compounds described in German Pat. No. 1,100,942, U.S. Pat. No. 3,490,911; the heteroatom-bonded alkyl compounds described in Japanese Pat. Exam. Pub. Nos. 29622/1969, 25373/1972, 24259/1972; the sulfonamides and esters described in Japanese Pat. O.P.I. Pub. No. 8736/1972; 1,3,5-tris[.beta.-(vinylsulfonyl)-propionyl]hexahydro-s-triazine described in Japanese Pat. O.P.I. Pub. No. 24435/1974; the alkyl compounds described in Japanese Pat. Exam. Pub. No. 35807/1975, Japanese Pat. O.P.I. Pub. No. 44164/1976; and the compounds described in Japanese Pat. O.P.I. Pub. No. 18944/1984.
These vinylsulfone-type hardeners are dissolved in water or in an organic solvent and added to photographic component layers, in a batch mode or an inline addition mode, in amounts of 0.005 to 20 wt %, preferably 0.02 to 10 wt % of binder such as gelatin, etc. The addition of hardeners is not limited to specific photographic component layers; it can be made applicable only to the uppermost layer or the lowermost layer, or to all the layers.
In one preferable embodiment of the invention, a compound represented by the following formula [B-1], [B-2] or [B-3] is contained in the light-sensitive material.
The compound represented by Formula [B-1], [B-2] or [B-3]is described hereunder.
Typical examples of the compound represented by Formula [B-1] are as follows: ##STR13##
Other examples include those exemplified on pages 130-132 of the specification of Japanese Pat. Appl. No. 274026/1990 by (B-1-4) to (B-1-15) and (B-1-17).
Some of the compounds represented by Formula [B-1] are known as antiseptics for citrus fruits and available on the market.
The compound represented by Formula [B-1] is used in amounts of 0.03 to 50 grams, preferably 0.12 to 10 grams and especially 0.15 to 5 grams per liter of the stabilizer of the invention.
Typical examples of the compound represented by Formula [B-2] or [B-3] are as follows, but not limited to them.
(B-2-1) 2-Methyl-4-isothiazoline-3-one
(B-2-2) 5-Chloro-2-methyl-4-isothiazoline-3-one
(B-2-3) 2-Methyl-5-phenyl-4-isothiazoline-3-one
(B-2-4) 4-Bromo-5-chloro-2-methyl-4-isothiazoline-3-one
(B-2-5) 2-Hydroxymethyl-4-isothiazoline-3-one
(B-2-6) 2-(2-Ethoxyethyl)-4-isothiazoline-3-one
(B-2-7) 2-(N-Methyl-carbamoyl)-4-isothiazoline-3-one
(B-2-8) 5-Bromomethyl-2-(N-dichlorophenyl-carbamoyl)-4-isothiazoline-3-one
(B-2-9) 5-Chloro-2-(2-phenylethyl)-4-isothiazoline-3-one
(B-2-10) 4-Methyl-2-(3,4-dichlorophenyl)-4-isothiazoline-3-one
(B-3-1) 1,2-Benzisothiazoline-3-one
(B-3-2) 2-(2-Bromoethyl)-1,2-benzisothiazoline-3-one
(B-3-3) 2-Methyl-1,2-benzisothiazoline-3-one
(B-3-4) 2-Ethyl-5-nitro-1,2-benzisothiazoline-3-one
(B-3-5) 2-Benzyl-1,2-benzisothiazoline-3-one
(B-3-6) 5-Chloro-1,2-benzisothiazoline-3-one
Syntheses and uses in other areas of these exemplified compounds are described in U.S. Pat. Nos. 2,767,172, 2,767,173, 2,767,174, 2,870,015, British Pat. No. 848,130, French Pat. No. 1,555,416, etc. Some of them are on the market under the trade names of Topcide 300 (Perma Chem Asia), Topcide 300 (Perma Chem Asia), Finecide J-700 (Tokyo Fine Chemicals Co.) and Proxel GXL (Imperial Chemical Ind. Ltd.).
The compounds represented by Formula [B-1], [B-2] or [B-3] are used, singly or in combination, in the range of 0.1 to 500 mg, preferably 0.5 to 100 mg per square meter of light-sensitive material.
The support of the color light-sensitive material to be processed by the method of the invention may be baryta paper; polyethylene-coated paper; polypropylene synthetic paper; transparent supports, such as glass plates, cellulose acetate film, cellulose nitrate film, polyester film such as polyethylene terephthalate, polyamide film, polycarbonate film, polystyrene film, which have a reflective layer or function as a reflective body by themselves; or other conventional transparent supports.
The invention can be applied to color light-sensitive materials such as color paper, color negative films, color reversal films, color reversal paper and direct positive color paper, which are for general use; films for movie use; and films for TV use.

EXAMPLES
The invention is illustrated by the following Examples, but the embodiment of the invention is not limited to these Examples.
EXAMPLE 1
Preparation of Silver Halide Color Photographic Light-sensitive Material (Color Paper)
A silver halide color photographic light-sensitive material was prepared by forming the following layers on the titanium-oxide-bearing side of a paper support laminated with polyethylene on one side and with titanium-oxide-containing polyethylene on the other side. The coating solutions used were prepared as follows:
Twenty-five grams of yellow coupler (Y-1), 98 g of dye image stabilizer (ST-1), 6.67 g of dye image stabilizer (ST-2) and 0.67 g of additive (HQ-1) were dissolved in 6.67 g of high boiling solvent (DNP) and 60 ml of ethyl acetate. The solution was then dispersed in 220 ml of 10% aqueous solution of gelatin containing 7 ml of 20% surfactant (SU-1) with a supersonic homogenizer to prepare a yellow coupler dispersion. The dispersion was mixed with a blue-sensitive silver halide emulsion (containing 9.8 g of silver) prepared under the following conditions to obtain a coating solution for the 1st layer.
Coating solutions for the 2nd to 7th layers were prepared likewise.
Further, hardener (H-1) was added to the 2nd and 4th layers, and hardener (H-2) to the 7th layer. As coating aids, surfactants (SU-2) and (SU-3) were added to regulate the surface tension.
TABLE 1______________________________________Layer Component Amount (g/m.sup.2)______________________________________7th layer gelatin 0.8(protective layer)6th layer (UV gelatin 0.33absorbing layer) UV absorbent (UV-1) 0.10 UV absorbent (UV-2) 0.04 UV absorbent (UV-3) 0.18 antistain agent (HQ-1) 0.01 DNP 0.18 PVP 0.03 anti-irradiation dye 0.02 (AI-2)5th layer (red- gelatin 1.21sensitive layer) red-sensitive silver 0.15 chlorobromide emulsion (EmC), in terms of Ag cyan coupler (C-1) 0.20 cyan coupler (C-2) 0.18 dye image stabilizer 0.20 (ST-1) antistain agent (HQ-1) 0.01 HBS-1 0.20 DOP 0.204th layer (UV gelatin 0.70absorbing layer) UV absorbent (UV-1) 0.28 UV absorbent (UV-2) 0.08 UV absorbent (UV-3) 0.38 antistain agent (HQ-1) 0.03 DNP 0.35______________________________________
TABLE 2______________________________________Layer Component Amount (g/m.sup.2)______________________________________3rd layer gelatin 1.40(green-sensitive green-sensitive silver 0.12layer) chlorobromide (green- sensitive emulsion (EmB), in terms of Ag magenta coupler (M-C) 0.30 dye image stabilizer 0.15 (ST-3) dye image stabilizer 0.15 (ST-4) dye image stabilizer 0.15 (ST-5) DNP 0.20 anti-irradiation dye 0.02 (AI-1)2nd layer gelatin 1.20(intermediate antistain agent (HQ-2) 0.19layer) DIDP 0.751st layer (blue- gelatin 1.20sensitive layer) blue-sensitive silver 0.19 chlorobromide emulsion (Em A), in terms of Ag yellow coupler (Y-1) 0.75 dye image stabilizer 0.30 (ST-1) dye image stabilizer 0.20 (ST-2) antistain agent (HQ-1) 0.02 anti-irradiation dye 0.02 (AI-3) DNP 0.20Support polyethylene laminated paper______________________________________ ##STR14##
Preparation of Blue-sensitive Silver Halide Emulsion
The following solutions (A) and (B) were simultaneously added to 1000 ml of 2% aqueous solution of gelatin kept at 40 C. over a period of 30 minutes, while controlling the pAg at 6.5 and the pH at 3.0. Then, the following solutions (C) and (D) were simultaneously added therein over a period of 180 minutes, while controlling the pAg at 7.3 and the pH at 5.5.
The pAg was controlled according to the method described in Japanese Pat. O.P.I. Pub. No. 45437/1984, and that of the pH was controlled by use of sulfuric acid or an aqueous solution of sodium hydroxide.
______________________________________Solution (A)Sodium chloride 3.42 gPotassium bromide 0.03 gWater was added to make 200 mlSolution (B)Silver nitrate 10 gWater was added to make 200 mlSolution (C)Sodium chloride 102.7 gPotassium bromide 1.0 gWater was added to make 600 mlSolution (D)Silver nitrate 300 gWater was added to make 600 ml______________________________________
After completing the addition, the resulting silver halide grains were subjected to desalting using a 5% aqueous solution of Demol N made by Kao Atlas Co. and a 20% aqueous solution of magnesium sulfate and, then, mixed with an aqueous solution of gelatin. Emulsion EMP-1 thus obtained comprised monodispersed cubic grains having an average grain size of 0.85 .mu.m, a coefficient of variation of grain size distribution of 7% and a silver chloride content of 99.5 mol %.
Blue-sensitive silver halide emulsion (Em-A) was prepared by subjecting emulsion EMP-1 to chemical sensitization for 90 minutes at 50.degree. C. using the following compounds:
______________________________________Sodium thiosulfate 0.8 mg/mol AgXChloroauric acid 0.5 mg/mol AgXStabilizer (STAB-1) 6 .times. 10.sup.-4 mol/mol AgXSensitizing dye (BS-1) 4 .times. 10.sup.-4 mol/mol AgXSensitizing dye (BS-2) 1 .times. 10.sup.-4 mol/mol AgX______________________________________
Preparation of Green-sensitive Silver Halide Emulsion
There was prepared emulsion EMP-2 comprising monodispersed cubic grains having an average grain size of 0.43 .mu.m, a coefficient of variation of grain size distribution of 8% and a silver chloride content of 99.5 mol %, in the same manner as emulsion EMP-1, except that the addition time of solutions (A) and (B) as well as that of solutions (C) and (D) were changed.
Green-sensitive silver halide emulsion (Em-B) was prepared by subjecting emulsion EMP-2 to chemical sensitization for 120 minutes at 55.degree. C. using the following compounds:
______________________________________Sodium thiosulfate 1.5 mg/mol AgXChloroauric acid 1.0 mg/mol AgXStabilizer (STAB-1) 6 .times. 10.sup.-4 mol/mol AgXSensitizing dye (BS-1) 4 .times. 10.sup.-4 mol/mol AgX______________________________________
Preparation of Red-sensitive Silver Halide Emulsion
There was prepared emulsion EMP-3 comprising monodispersed cubic grains having an average grain size of 0.50 .mu.m, a coefficient of variation of grain size distribution of 8% and a silver chloride content of 99.5 mol % as emulsion EMP-1, except that the addition time of solutions (A) and (B) as well as that of solutions (C) and (D) were changed.
Red-sensitive silver halide emulsion (Era-C) was prepared by subjecting emulsion EMP-3 to chemical sensitization for 90 minutes at 60.degree. C. using the following compounds:
__________________________________________________________________________Sodium thiosulfate 1.8 mg/mol AgXChloroauric acid 2.0 mg/mol AgXStabilizer (STAB-1) 6 .times. 10.sup.-4 mol/mol AgXSensitizing dye (BS-1) 4 .times. 10.sup.-4 mol/mol AgXBS-1 ##STR15##BS-2 ##STR16##GS-1 ##STR17##RS-1 ##STR18##STAB-1 ##STR19##__________________________________________________________________________
This light-sensitive material sample was exposed according to the usual manner and then processed using the following processes and processing solutions.
______________________________________ Processing Processing ReplenishProcess Temp. Time ing Rate______________________________________(1) Color developing 40.0 .+-. 0.3.degree. C. 20 sec 55 ml/m.sup.2(2) Bleach-fixing 40.0 .+-. 0.5.degree. C. 25 sec 60 ml/m.sup.2(3) Stabilizing 30 to 40.degree. C. 90 sec 200 ml/m.sup.2 (three-tank cascade)(4) Drying 60 to 80.degree. C. 30 sec --______________________________________[Color Developer]Triethanolamine 10 gDiethylene glycol 10 gN,N-Diethylhydroxylamine 3.6 gHydrazinodiacetic acid 5.0 gPotassium bromide 20 mgPotassium chloride 3.5 gDiethylenetriaminepentaacetic acid 5 gPotassium sulfite 0.2 gColor developing agent (3-methyl-4-amino-N-ethyl-N- 5.5 g(.beta.-methanesulfonamidoethyl)-aniline sulfate)Potassium carbonate 25 gPotassium hydrogencarbonate 5 g______________________________________
Water was added to make 1000 ml, and the pH was adjusted to 10.10 with potassium hydroxide or sulfuric acid.
______________________________________[Color Developing Replenisher]______________________________________Triethanolamine 14.0 gDiethylene glycol 12 gN,N-Diethylhydroxylamine 5 gHydrazinodiacetic acid 7.5 gPotassium chloride 0.1 gDiethylenetriaminepentaacetic acid 7.5 gPotassium sulfite 0.3 gColor developing agent (3-methyl-4-amino-N-ethyl-N- 11.3 g(.beta.-methanesulfonamidoethyl)-aniline sulfate)Potassium carbonate 30 gPotassium hydrogencarbonate 1 g______________________________________
Water was added to make 1000 ml, and the pH was adjusted to 10.65 with potassium hydroxide or sulfuric acid.
______________________________________[Bleach-fixer]______________________________________Ferric complex salts of organic acids 0.2 mol(see Table 3)Ammonium thiosulfate 100 gSodium sulfite 10 gSodium metabisulfite 1.5 g______________________________________
Water was added to make 1000 ml, and the pH was adjusted to 7.0 with a 25% aqueous ammonia and acetic acid.
Bleach-fixing Replenisher
The concentration of each component was made 1.25 times that of the above bleach-fixer and the pH was adjusted to 5.3.
______________________________________[Stabilizer and Stabilizing Replenisher]______________________________________Ortho-phenylphenol 0.1 gMST (a stilbene diphosponic acid derivative 1.0 gproduct of Ciba-Geigy AG)ZnSO4 0.8 gAmmonium sulfite (40% solution) 5.0 ml1-Hydroxyethylidene-1,1-diphosphonic acid 10 g(60% solution)Ethylenediaminetetracetic acid 1.5 g______________________________________
The pH was adjusted to 7.8 with aqueous ammonia or sulfuric acid and water was added to make 1000 ml.
The overflown liquid of the bleach-fixer was collected in a tank; when the tank was filled with the overflown liquid, the regenerant of the following recipe (addition amounts are for 1000 ml of overflow) was added to it. The regenerated overflow was then reused as replenisher.
______________________________________[Regenerant]______________________________________Ferric complex salts of organic acids (see Table 3) 0.052 molAmmonium thiosulfate 30 gSodium sulfite 15 g______________________________________
The pH was adjusted to 5.3 with acetic acid.
The continuous processing was run until the above regenerating process was repeated 30 times.
After the processing, the processed sample was subjected to X-ray fluorescence analysis to determine the residual amount of silver in the exposed portion; it was further checked visually for stains on edge portions. The bleach-fixer tank solution after the processing was visually checked for possible sulfide formation. The evaluation results are shown in Table 3.
In Table 3, the letters in the column of sulfide formation have the following meanings:
A: no sulfides are observed at all.
B: very slight floating matters are observed on the liquid surface.
C: faint formation of sulfides is observed.
D: obvious formation of sulfides is observed.
E: heavy formation of sulfides are observed.
The letters in the column of edge stain have the following meanings:
A: no edge stains are observed at all.
B: very slight edge stains are observed.
C: slight edge stains are observed.
D: obvious edge stains are observed.
E: heavy edge stains are observed.
TABLE 3______________________________________ Ferric Amount of For- Complex Residual mationExperi- Salt Silver ofment of Organic (mg/100 Edge Sul-No. Acid cm.sup.2) Stain fides Remarks______________________________________1-1 EDTA-Fe 1.0 C D Comparison1-2 PDTA-Fe 2.1 C E Comparison1-3 DTPA-Fe 0.6 E B Comparison1-4 NTA-Fe 1.5 C D Comparison1-5 CyDTA-Fe 1.3 C D Comparison1-6 (A-I-1)-Fe 0.6 B B Invention1-7 (A-I-2)-Fe 0.6 B B Invention1-8 (A-II-1)-Fe 0.4 A A Invention1-9 (A-II-3)-Fe 0.3 A A Invention 1-10 (A-II-14)-Fe 0.4 A A Invention 1-11 (A-III-1)-Fe 0.6 B B Invention 1-12 (A-III-2)-Fe 0.7 B B Invention 1-13 (A-III-6)-Fe 0.7 B B Invention______________________________________
In Table 3 and the tables that follow, EDTA-Fe is ammonium ferric ethylenediaminetetraacetate; PDTA-Fe, ammonium ferric 1,3-propylenediaminetetraacetate; DTPA-Fe, ammonium ferric diethylenetriaminepentaacetate; NTA-Fe, ammonium ferric nitrilotriacetate; CyDTA-Fe, ammonium ferric cyclohexanetetracetate; (A-I-1)-Fe represents ammonium ferric complex salt of exemplified compound (A-I-1), and (A-I-2)-Fe, (A-II-1)-Fe, (A-II-3) -Fe, (A-II-14) -Fe, (A-III-1) -Fe, (A-III-2)-Fe and (A-III-6)-Fe each have the same meaning.
It can be understood from Table 3 that use of the ferric complex salt of organic acids according to the invention provides an image low in residual silver and less in edge staining as well as an improved preservability of a bleach-fixer.
EXAMPLE 2
In the following examples, addition amounts in a silver halide light-sensitive material are in grams per square meter unless otherwise indicated. Amounts of silver halides and colloidal silvers are given in amounts of silver present. A silver iodobromide color photographic light-sensitive material was prepared in the following way. Silver Iodobromide Color Photographic Light-sensitive Material
A 60-.mu.m thick polyethylene terephthalate film support was subbed on one side. Then, the following two layers were formed in order on the support opposite to the subbed side (on the unsubbed side).
______________________________________Reverse 1st layerAlumina Sol AS-100 (aluminium oxide made by 0.8 gNissan Chemical Ind.)Reverse 2nd layerDiacetylcellulose 100 mgStearic acid 10 mgSilica fine powder (average particle size: 0.2 .mu.m) 50 mg______________________________________
Subsequently, multilayered color photographic light-sensitive material (a-1) was prepared by forming the following layers in order on the subbed side of the support.
______________________________________1st layer: antihalation layer (HC)Black colloidal silver 0.15 gUV absorbent (UV-1) 0.20 gColored cyan coupler (CC-1) 0.02 gHigh boiling solvent (Oil-1) 0.20 gHigh boiling solvent (Oil-2) 0.20 gGelatin 1.6 g2nd layer: intermediate layer (IL-1)Gelatin 1.3 g3rd layer: low-speed red-sensitive emulsion layer (R-1)Silver iodobromide emulsion 0.4 g(average grain size: 0.3 .mu.m)Silver iodobromide emulsion 0.3 g(average grain size: 0.4 .mu.m)Sensitizing dye (S-1) 3.0 .times. 10.sup.-4 (mol/mol Ag)Sensitizing dye (S-2) 3.2 .times. 10.sup.-4 (mol/mol Ag)Sensitizing dye (S-3) 0.3 .times. 10.sup.-4 (mol/mol Ag)Cyan coupler (C-1) 0.50 gCyan coupler (C-2) 0.20 gColored cyan coupler (CC-1) 0.07 gDIR compound (D-1) 0.006 gDIR compound (D-2) 0.01 gHigh boiling solvent (Oil-1) 0.55 gGelatin 1.0 g4th layer: high-speed red-sensitive emulsion layer (R-H)Silver iodobromide emulsion 0.9 g(average grain size: 0.7 .mu.m)Sensitizing dye (S-1) 1.7 .times. 10.sup.-4 (mol/mol Ag)Sensitizing dye (S-2) 1.6 .times. 10.sup.-4 (mol/mol Ag)Sensitizing dye (S-3) 0.2 .times. 10.sup.-4 (mol/mol Ag)Cyan coupler (C-2) 0.23 gColored cyan coupler (CC-1) 0.03 gDIR compound (D-2) 0.02 gHigh boiling solvent (Oil-1) 0.30 gGelatin 1.0 g5th layer: intermediate layer (IL-2)Gelatin 0.8 g6th layer: low-speed green-sensitive emulsion layer (G-L)Silver iodobromide emulsion 0.6 g(average grain size: 0.4 .mu.m)Silver iodobromide emulsion 0.2 g(average grain size: 0.3 .mu.m)Sensitizing dye (S-4) 6.7 .times. 10.sup.-4 (mol/mol Ag)Sensitizing dye (S-5) 1.0 .times. 10.sup.-4 (mol/mol Ag)Magenta coupler (M-A) 0.20 gMagenta coupler (M-B) 0.40 gColored magenta coupler (CM-1) 0.10 gDIR compound (D-3) 0.02 gHigh boiling solvent (Oil-2) 0.7 gGelatin 1.0 g7th layer: high-speed green-sensitive emulsion layer (G-H)Silver iodobromide emulsion 0.9 g(average grain size: 0.7 .mu.m)Sensitizing dye (S-6) 1.1 .times. 10.sup.-4 (mol/mol Ag)Sensitizing dye (S-7) 2.0 .times. 10.sup.-4 (mol/mol Ag)Sensitizing dye (S-8) 0.5 .times. 10.sup.-4 (mol/mol Ag)Magenta coupler (M-A) 0.5 gMagenta coupler (M-B) 0.13 gColored magenta coupler (CM-1) 0.04 gDIR compound (D-3) 0.004 gHigh boiling solvent (Oil-2) 0.35 gGelatin 1.0 g8th layer: yellow filter layer (YC)Yellow colloidal silver 0.1 gAdditive (HS-1) 0.07 gAdditive (HS-2) 0.07 gAdditive (SC-1) 0.12 gHigh boiling solvent (Oil-2) 0.15 gGelatin 0.9 g9th layer: low-speed blue-sensitive emulsion layer (B-H)Silver iodobromide emulsion 0.25 g(average grain size: 0.3 .mu.m)Silver iodobromide emulsion 0.25 g(average grain size: 0.4 .mu.m)Sensitizing dye (S-9) 5.8 .times. 10.sup.-4 (mol/mol Ag)Yellow coupler (Y-1) 0.71 gYellow coupler (Y-2) 0.30 gDIR compound (D-1) 0.003 gDIR compound (D-2) 0.006 gHigh boiling solvent (Oil-2) 0.18 gGelatin 1.2 g10th layer: high-speed blue-sensitive emulsion layer (B-H)Silver iodobromide emulsion 0.5 g(average grain size: 0.8 .mu.m)Sensitizing dye (S-10) 3 .times. 10.sup.-4 (mol/mol Ag)Sensitizing dye (S-11) 1.2 .times. 10.sup.-4 (mol/mol Ag)Yellow coupler (Y-1) 0.18 gYellow coupler (Y-2) 0.20 gHigh boiling solvent (Oil-2) 0.05 gGelatin 0.9 g11th layer: 1st protective layer (PRO-1)Silver iodobromide (average grain 0.3 gsize: 0.08 .mu.m)UV absorbent (UV-1) 0.07 gUV absorbent (UV-2) 0.10 gAdditive (HS-1) 0.2 gAdditive (HS-2) 0.1 gHigh boiling solvent (Oil-1) 0.07 gHigh boiling solvent (Oil-3) 0.07 gGelatin 0.85 g12th layer: 2nd protective layer (PRO-2)Compound A 0.04 gCompound B 0.004 gPolymethylmethacrylate (average 0.02 gparticle size: 3 .mu.m)Methyl methacrylate-ethyl 0.13 gmethacrylate-methacrylic acid3:3:4 (weight ratio) copolymer(average particle size: 3 .mu.m)______________________________________
Besides the above components, this color photographic light-sensitive material contained compounds (Su-1) and (Su-2), viscosity regulator, hardeners (H-1) and (H-2), stabilizer (ST-1), antifoggants (AF-1) and (AF-2) having molecular weights of 10,000 and 1,100,000, respectively, dyes (AI-1) and (AI-2), and compound (DI-1) (9.4 mg/m.sup.2). ##STR20##
Preparation of Emulsion
The silver iodobromide emulsion used in the 10th layer was prepared in the following manner:
A silver iodobromide emulsion was prepared by the double-jet method using monodispersed silver iodobromide grains having an average grain size of 0.33 .mu.m (silver iodobromide content: 2 mol %) as seed crystal grains.
While stirring solution <G-1> kept at 70.degree. C. pAg 7.8 and pH 7.0, the seed emulsion was added thereto in an amount equivalent to 0.34 mole.
(Formation of Inner High-iodide Phase or Core Phase)
Then, solutions <H-1> and <S-1> were added thereto over a period of 86 minutes, at an accelerated addition rate (the final addition rate was 3.6 times the initial addition rate), with their flow ratio kept at 1:1.
Formation of Outer Low-iodide Phase or Shell Phase
Subsequently, while keeping the pAg at 10.1 and pH at 6.0 solutions <H-2> and <S-2> were added over a period of 65 minutes, at an accelerated addition rate (the final addition rate was 5.2 times the initial addition rate), with their flow ratio kept at 1:1.
During this grain formation, the pAg and pH were controlled by use of an aqueous solution of potassium bromide and 56% aqueous acetic acid. After grains were formed, they were subjected to washing treatment by the usual flocculation method and, then, mixed with gelatin for redispersing. This dispersion was adjusted to pH 5.8 and pAg 8.06 at 40.degree. C.
The resulting emulsion comprised monodispersed octahedral silver iodobromide grains having an average grain size of 0.80 .mu.m, a coefficient of variation of grain size distribution of 12.4% and a silver iodide content of 9.0 mol %.
______________________________________Solution <G-1>Ossein gelatin 100.0 g10-wt % Methanol solution of compound-1 25.0 ml28% Aqueous ammonia 440.0 ml56% Aqueous acetic acid 660.0 mlWater is added to make 5000.0 mlSolution <H-1>Ossein gelatin 82.4 gPotassium bromide 151.6 gPotassium iodide 90.6 gWater is added to make 1030.5 mlSolution <S-1>Silver nitrate 309.2 g28% Aqueous ammonia equivalentWater is added to make 1030.5 mlSolution <H-2>Ossein gelatin 302.1 gPotassium bromide 770.0 gPotassium iodide 33.2 gWater is added to make 3776.8 mlSolution <S-2>Silver nitrate 1133.0 g28% Aqueous ammonia equivalentWater is added to make 3776.8 ml______________________________________ The chemical structure of compound1 used in solution <G1> is as follows: Compound1 ##STR21## (1300 = approx. average molecular weight)
The above emulsions different in average grain size and silver iodide content were prepared by altering average size of seed crystals, temperature, pAg, pH, addition rate, addition time and halide composition, respectively.
Each resulting emulsion was a core/shell-type monodispersed one having a coefficient of variation of grain size distribution not more than 20%. Each emulsion was subjected to chemical ripening, under optimum conditions, in the presence of sodium thiosulfate, chloroauric acid and ammonium thiocyanate. Then, the sensitizing dyes, 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene, and 1-phenyl-5-mercaptotetrazole were added thereto.
In the preparation of this silver iodobromide color light-sensitive material, the average silver iodide content was adjusted to 8 mol %.
The light-sensitive material so prepared was exposed wedgewise by the usual method and then subjected to continuous processing in the following procedure:
______________________________________ Processing Processing ReplenishingProcess Time Temp. Rate*______________________________________Color developing 3 min 15 sec 38.degree. C. 18 ml(1 tank)Bleaching (1 tank) 60 sec 38.degree. C. 4 mlFixing (1 tank) 1 min 38.degree. C. 15 mlStabilizing 1 min 38.degree. C. 30 ml(3-tank cascade)Drying 40-80.degree. C. 1 min -- --Color Developing SolutionPotassium carbonate 30 gSodium hydrogencarbonate 2.5 gPotassium sulfite 3.0 gSodium bromide 1.3 gPotassium iodide 0.6 mgHydroxylamine sulfate 2.5 gSodium chloride 0.6 g4-Amino-3-methyl-N-ethyl-N-(.beta.-hydroxylethyl) 4.5 ganiline sulfateDiethylenetriaminepentaacetic acid 3.0 gPotassium hydroxide 1.2 g______________________________________ *Amounts per roll of film (135 size, 24 exposures)
Water is added to make 1000 ml, and the pH is adjusted to 10.00 with potassium hydroxide or 20% sulfuric acid.
______________________________________Color Developing Replenisher______________________________________Potassium carbonate 35 gSodium hydrogencarbonate 3 gPotassium sulfite 5 gSodium bromide 0.3 gHydroxylamine sulfate 3.5 g4-Amino-3-methyl-N-ethyl-N-(.beta.-hydroxylethyl) 6.0 ganiline sulfatePotassium hydroxide 2 gDiethylenetriaminepentaacetic acid 3.0 g______________________________________
Water was added to make 1000 ml, and the pH was adjusted to 10.20 with potassium hydroxide or 20% sulfuric acid.
______________________________________Bleaching Tank Solution______________________________________Ferric complex salts of organic acids 0.35 mol(described in Table 4)Ethylenediaminetetraacetic acid 2.0 gAmmonium bromide 1.0 molGlacial acetic acid 50 ml______________________________________
The pH was adjusted to 4.2 with aqueous ammonia or acetic acid, and then water was added to make 1000 ml.
Bleach-replenisher
The concentration of each component is made 1.2 times that of the bleaching tank solution, and the pH is adjusted to 3.0.
______________________________________Fixer (Tank Solution and Replenisher)______________________________________Ammonium thiosulfate (70% solution) 350 mlAmmonium thiocyanate 20 gAnhydrous sodium bisulfite 12 gSodium metabisulfite 2.5 gDisodium ethylenediaminetetraacetate 0.5 g______________________________________
Water was added to make 1000 ml, and the pH was adjusted to 6.0 with acetic acid and aqueous ammonia.
______________________________________Stabilizer (Tank Solution and Replenisher)______________________________________Hexamethylenetetramine 5 gDiethylene glycol 2 gp-C.sub.9 H.sub.19 --C.sub.6 H.sub.4 --(OCH.sub.2 CH.sub.2).sub.10 2 gH______________________________________
The pH was adjusted to 8.0 with potassium hydroxide, and water was added to make 1000 ml.
The above regenerating procedure was repeated 35 times while running the processing continuously.
After the continuous processing was completed, the amount of residual silver as well as the yellow fog density of unexposed portion on the processed light-sensitive material were examined; formation of sulfides in the fixer was also checked as in Example 1.
The results obtained are shown in Table 4, in which the letters A to E mean the same as those in Table 3.
TABLE 4__________________________________________________________________________ Ferric Amount of Yellow Fog Formation Complex Salt Residual Density of ofExperiment of Organic Silver Unexposed SulfidesNo. Acid (mg/100 cm.sup.2) Portion in Fixer Remarks__________________________________________________________________________2-1 EDTA-Fe 10.5 0.05 C Comparison2-2 PDTA-Fe 0.5 0.27 E Comparison2-3 DTPA-Fe 12.6 0.04 B Comparison2-4 NTA-Fe 6.3 0.03 B Comparison2-5 CyDTA-Fe 7.1 0.04 B Comparison2-6 (A-I-1)-Fe 0.6 0.03 A Invention2-7 (A-I-2)-Fe 0.5 0.03 A Invention2-8 (A-II-1)-Fe 0.8 0.03 A Invention2-9 (A-II-3)-Fe 0.8 0.04 A Invention2-10 (A-II-14)-Fe 0.7 0.03 A Invention2-11 (A-III-1)-Fe 0.9 0.04 B Invention2-12 (A-III-2)-Fe 0.8 0.03 B Invention2-13 (A-III-6)-Fe 0.9 0.03 B Invention__________________________________________________________________________
It can be understood from Table 4 that use of the organic acid ferric complex salt of the invention exerts favorable effects in reducing the amount of residual silver, controlling the rise in yellow fog density of unexposed portions and improving the preservability of a fixer.
EXAMPLE 3
According to 301C Amended MITI Test (I) adopted on May 12, 1981, by OECD as the guideline for testing chemical substances, biodegradabilities were determined on photographic chelating agents including ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA), N-hydroxyethyl-ethylenediaminetetraacetic acid (HEDTA), and exemplified compounds (A-I-1), (A-I-2) , (A-II-1) , (A-II-3) , (A-II-14), (A-III-1), (A-III-6).
As a result, it was found that while the ferric salts of EDTA, DTPA and HEDTA were hardly decomposed biologically, the ferric salts of the chelating agents according to the invention were highly biodegradable and, thereby, proved to be high in environmental suitability.
EXAMPLE 4
Experiments were carried out in the same manner as in Experiment Nos. 1-6, 1-8 and 1-11 of Example 1, except that magenta coupler (M-C) used in Example 1 was replaced by exemplified magenta couplers (M-5), (M-8), (M-11), (M-9), (M-12), (M-13), (M-7) and (M-4), respectively. The results showed that the amount of residual silver was decreased by 20 to 25%, and that the whiteness of unexposed portions was also improved.
EXAMPLE 5
Experiments were made in the same manner as in Experiment Nos. 2-6, 2-8 and 2-11 of Example 2, except that magenta couplers (M-A) and (M-B) used in Example 2 were replaced by exemplified magenta couplers (M-2), (M-6), (M-8), (M-1), (M-10) and (M-3), respectively. A 20-25% decrease in amount of residual silver and a 40% decrease in yellow fog density were observed.
The overflown liquid of the bleach was collected in a tank. And a regenerant having the following composition (amounts are for 1000 ml of overflown liquid) was added thereto, when the tank was filled with the overflown liquid.
______________________________________[Regenerator]______________________________________Organic acid ferric complex salt (see Table 4) 0.05 molEthylenediaminetetraacetic acid 3.0 gAmmonium bromide 0.08 mol______________________________________
The pH was adjusted to 3.0 with acetic acid.
EXAMPLE 6
Experiments were carried out in the same manner as in Experiment Nos. 2-6 and 2-7 of Example 2, except that the ratio of ammonium ions to the total cations contained in the bleach of Example 2 was varied as shown in Table 5 by replacing the cations of the compounds added to the bleach with ammonium ions or potassium ions.
The results are summarized in Table 5.
TABLE 5______________________________________ Percentage of Ammonium Yellow FogExperi- Ions to Total Cations Organic Acid Densityment contained in Bleach Ferric in UnexposedNo. (mol %) Complex Salt Portion______________________________________6-1 100 (A-I-1)-Fe 0.036-2 60 (A-I-1)-Fe 0.036-3 50 (A-I-1)-Fe 0.026-4 30 (A-I-1)-Fe 0.016-5 10 (A-I-1)-Fe 0.016-6 0 (A-I-1)-Fe 0.016-7 100 (A-I-2)-Fe 0.036-8 60 (A-I-2)-Fe 0.036-9 50 (A-I-2)-Fe 0.026-10 30 (A-I-2)-Fe 0.016-11 10 (A-I-2)-Fe 0.016-12 0 (A-I-2)-Fe 0.01______________________________________
As is shown in the table, there were little differences in amounts of residual silver and in formation of sulfides in the bleach. It was also found that the effect of the invention could be better brought out when the ratio of ammonium ions to the total cations contained in the bleach was not more than 50 mol %.
EXAMPLE 7
Experiments were carried out in the same manner as in Experiment No. 2-6 of Example 2, except that hardeners (H-1) and (H-2) used in Example 2 were replaced by the hardeners shown in Table 6.
The results are summarized in Table 6.
TABLE 6______________________________________ Yellow Fog Density inExperiment No. Hardener Unexposed Portion______________________________________7-1 Exemplified (VS-2) 0.027-2 Exemplified (VS-4) 0.017-3 Exemplified (VS-6) 0.027-4 Exemplified (VS-9) 0.027-5 Exemplified (VS-10) 0.027-6 Exemplified (VS-12) 0.037-7 Exemplified (VS-22) 0.027-8 Exemplified (VS-33) 0.027-9 Exemplified (VS-54) 0.017-10 Following RH-1 0.067-11 Following RH-2 0.077-12 Following RH-3 0.067-13 Following RH-4 0.057-14 Following RH-5 0.08______________________________________
The chemical structures of hardeners RH-1, RH-2, RH-3, RH-4 and RH-5 shown in Table 6 are as follows: ##STR22##
As is apparent from Table 6, there is no significant difference in amounts of residual silver and in formation of sulfides. Further, the effect of the invention is better brought out when the vinylsulfone-type hardener is used in the processing according to the invention.
EXAMPLE 8
Experiments were conducted in the same way as in Experiment No. 2-7 of Example 2, except that one of the compounds shown in Table 7 was contained in the color negative film used in Experiment No. 2-7 in an amount of 10 mg/m2.
The results obtained are shown in Table 7.
TABLE 7______________________________________ Yellow Fog Density of Formation ofExperiment Unexposed Sulfides inNo. Additive (10 mg/m.sup.2) Portion Fixer______________________________________8-1 Not added 0.07 C8-2 Phenol 0.06 B8-3 Dehydroacetic acid 0.06 B8-4 Thiazolyl 0.07 B benzimidazole8-5 Chlorodiphenyl 0.07 B8-6 Cresol 0.06 B8-7 p-Amino- 0.05 B benzenesulfamide8-8 (B-1-1) 0.03 A8-9 (B-1-16) 0.03 A8-10 (B-1-18) 0.03 A8-11 (B-2-1) 0.02 A8-12 (B-2-2) 0.03 A8-13 (B-2-7) 0.02 A8-14 (B-2-10) 0.02 A8-15 (B-3-1) 0.02 A8-16 (B-3-6) 0.02 A______________________________________
It can be understood from Table 7 that the effect of the invention can be better brought out by incorporating the compound represented by the foregoing formula [B-1], [B-2] or [B-3] in the light-sensitive material to be processed by the method of the invention.
EXAMPLE 9
Preparation of Silver Halide Color Photographic Light-sensitive Material (Color Paper)
A multilayered color photographic light-sensitive material was prepared by forming the following component layers on the titanium-oxide-bearing side of a paper support laminated with titanium-oxide-containing polyethylene on one side and with polyethylene on the other side. The coating solutions were prepared as follows:
Coating solution for 1st layer
A mixture of 27.3 g of yellow coupler (Y-1), 10 g of dye image stabilizer (ST-1), 6.67 g of dye image stabilizer (ST-2), 0.67 g of additive (HQ-1) and 6.67 g of high boiling solvent (DNP) was dissolved in 60 ml of ethyl acetate. The solution was dispersed, with a supersonic homogenizer, in 220 ml of 10% aqueous solution of gelatin containing 7 ml of 20% aqueous solution of surfactant (SU-1) to obtain a yellow coupler dispersion. Then, the dispersion was mixed with a blue-sensitive silver halide emulsion (containing 8.3 g of silver) prepared under conditions described later, so that a coating solution for the 1st layer was prepared.
Coating solutions for the 2nd to 7th layers were prepared likewise. Further, hardener (H-1) was added to the 2nd and 4th layers, and hardener (H-2) to the 7th layer. As coating aids, surfactants (SU-2) and (SU-3) were added to adjust the surface tension.
TABLE 8______________________________________Layer Component Amount (g/m.sup.2)______________________________________7th layer gelatin 1.0(protective layer)6th layer (UV gelatin 0.35absorbing layer) UV absorbent (UV-1) 0.10 UV absorbent (UV-2) 0.04 UV absorbent (UV-3) 0.18 antistain agent (HQ-1) 0.01 DNP 0.18 PVP 0.03 anti-irradiation dye 0.02 (AI-2)5th layer (red- gelatin 1.21sensitive layer) red-sensitive silver 0.19 chlorobromide emulsion (Em-C), in terms of Ag cyan coupler (C-1) 0.20 cyan coupler (C-2) 0.25 dye image stabilizer 0.20 (ST-1) antistain agent (HQ-1) 0.01 HBS-1 0.20 DOP 0.204th layer (UV gelatin 0.90absorbing layer) UV absorbent (UV-1) 0.28 UV absorbent (UV-2) 0.08 UV absorbent (UV-3) 0.38 antistain agent (HQ-1) 0.03 DNP 0.35______________________________________
TABLE 9______________________________________Layer Component Amount (g/m.sup.2)______________________________________3rd layer gelatin 1.40(green- green-sensitive silver 0.15sensitive layer) chlorobromide emulsion (Em-B), in terms of Ag magenta coupler (M-C) 0.32 dye image stabilizer 0.15 (ST-3) dye image stabilizer 0.15 (ST-4) dye image stabilizer 0.15 (ST-5) DNP 0.20 anti-irradiation dye 0.02 (AI-1)2nd layer gelatin 1.20(intermediate antistain agent (HQ-2) 0.12layer) DIDP 0.151st layer gelatin 1.20(blue-sensitive blue-sensitive silver 0.25layer) chlorobromide emulsion (Em-A), in terms of Ag yellow coupler (Y-1) 0.82 dye image stabilizer 0.30 (ST-1) dye image stabilizer 0.20 (ST-2) antistain agent (HQ-1) 0.02 anti-irradiation dye 0.02 (AI-3) DNP 0.20Support polyethylene laminated paper______________________________________
This sample was exposed by the usual method and then processed by use of the following processes and processing solutions.
______________________________________ Processing Processing Replenishing Process Temp. Time Rate______________________________________(1) Color 35.0 .+-. 0.3.degree. C. 45 sec 162 ml/m.sup.2 developing(2) Bleach-fixing 35.0 .+-. 0.5.degree. C. 45 sec see Tables 10 to 12(3) Stabilizing 30 to 34.degree. C. 90 sec 248 ml/m.sup.2 (three-tank cascade)(4) Drying 60 to 80.degree. C. 30 sec --Color DeveloperTriethanolamine 10 gEthylene glycol 6 gN,N-Diethylhydroxylamine 3.6 gHydrazinodiacetic acid 5.0 gPotassium bromide 20 mgPotassium chloride 2.5 gDiethylenetriaminepentaacetic acid 5 gPotassium sulfite 5.0 .times. 10.sup.-4 molColor developing agent (3-methyl- 5.5 g4-amino-N-ethyl-N-(.beta.-methanesulfonamidoethyl)-aniline sulfate)Potassium carbonate 25 gPotassium hydrogencarbonate 5 g______________________________________
Water was added to make 1000 ml, and the pH was adjusted to 10.10 with potassium hydroxide or sulfuric acid.
______________________________________Color Developing Replenisher______________________________________Triethanolamine 14.0 gEthylene glycol 8.0 gN,N-Diethylhydroxylamine 5 gHydrazinodiacetic acid 7.5 gPotassium bromide 8 mgPotassium chloride 0.3 gDiethylenetriaminepentaacetic acid 7.5 gPotassium sulfite 7.0 .times. 10.sup.-4 molColor developing agent (3-methyl-4-amino- 8 gN-ethyl-N-(.beta.-methanesulfonamidoethyl)-aniline sulfate)Potassium carbonate 30 gPotassium hydrogencarbonate 1 g______________________________________
Water was added to make 1000 ml, and the pH was adjusted to 10.40 with potassium hydroxide or sulfuric acid.
______________________________________Bleach-fixer______________________________________Water 600 mlOrganic acid ferric complex salt 0.15 mol(described in Tables 10 to 12)Thiosulfate 0.6 molSulfite 0.15 mol1,3-propanediaminetetraacetic acid 2 g______________________________________
The pH was adjusted to 7.0 with aqueous ammonia, potassium hydroxide or acetic acid, and water was added to make 1000 ml.
Bleach-fixing Replenisher
The concentration of each component was raised to the value shown in Tables 10 to 12, and the pH was adjusted to 5.0.
______________________________________Stabilizer and Stabilizing Replenisher______________________________________Ortho-phenylphenol 0.1 gMST (product of Ciba-Geigy AG) 1.0 gZnSO.sub.4.7H.sub.2 O 0.1 gAmmonium sulfite (40% solution) 5.0 ml1-Hydroxyethylidene-1,1-diphosphonic acid 3.0 g(60% solution)Ethylenediaminetetraacetic acid 1.5 g______________________________________
The pH was adjusted to 7.8 with aqueous ammonia or sulfuric acid and water was added to make 1000 ml.
A continuous processing was run by use of the color paper and processing solutions prepared as above.
In running the continuous processing, tanks of an automatic processor were filled with the above color developing tank solution, bleach-fixing tank solution and stabilizing tank solution. And, while carrying on processing of the color paper, the above color developing replenisher (replenishing rate: 80 ml/m.sup.2), bleach-fixing replenisher (replenishing rate: shown in Tables 10 to 12) and stabilizing replenisher (replenishing rate: 250 ml/m.sup.2) were replenished through metering pumps at intervals of 3 minutes.
This continuous processing was carried on, at a daily processing amount of 0.05 R, till the volume of bleach-fixer replenished to the bleach-fixer tank reached 3 times the capacity of the bleach-fixer tank. Here, 1 R means that the bleach-fixer is replenished up to a volume equal to the capacity of the bleach-fixing tank.
The exposed portion of the processed sample was divided into two parts. One was subjected to X-ray fluorescence analysis for determining the amount of residual silver. The other was used for measuring R density and then rebleached in an aqueous solution of ethylenediaminetetracetic acid ferric complex salt (100 g/l, pH 6.5). R density after the rebleaching was measured to determine the recoloring property (measured value before rebleaching--measured value after rebleaching). The processed color paper was also checked for stains on the edge portion. Further, formation of sulfides was visually examined on the bleach-fixing tank solution and bleach-fixing replenisher after completion of the processing. The results are shown in Tables 10 to 12.
In Tables 10 to 12, the letters in the column of sulfide formation have the following meanings:
A: no sulfides are observed at all.
B: very slight floating matters are observed on the liquid surface.
C: faint formation of sulfides are observed.
D: obvious formation of sulfides are observed.
E: heavy formation of sulfides are observed, and the tank wall is tinged yellow.
The letters in the column of edge stain have the following meanings:
A: no edge stains are observed at all.
B: very slight edge stains are observed.
C: slight edge stains are observed.
D: obvious edge stains are observed.
E: heavy edge stains are observed.
In Table 10, EDTA-Fe is an ethylenediaminetetraacetic acid ferric complex salt; PDTA-Fe, 1,3-propylenediaminetetraacetic acid ferric complex salt; DTPA-Fe, diethylenetriaminepentaacetic acid ferric complex salt.
TABLE 10__________________________________________________________________________ Organic Amount of Formation of Acid Ferric Bleach-fixer Bleach-fixing Residual SulfidesExperiment Complex Replenisning Replenisher Silver Recoloring Edge Tank Repleni-No. Salt Rate (ml/m.sup.2) Concentration (mg/100 cm.sup.2) Property Effect Solution sher__________________________________________________________________________9-1 EDTA-Fe 400 Tank 0.0 0.0 A A B(Comparison) solution .times. 1.19-2 EDTA-Fe 200 Tank 0.2 0.0 A B B(Comparison) solution .times. 1.29-3 EDTA-Fe 100 Tank 0.8 -0.12 B D D(Comparison) solution .times. 1.49-4 EDTA-Fe 50 Tank 1.2 -0.18 C D D(Comparison) solution .times. 1.89-5 EDTA-Fe 25 Tank 1.4 -0.22 C E E(Comparison) solution .times. 2.69-6 EDTA-Fe 15 Tank 1.7 -0.25 C E E(Comparison) solution .times. 3.09-7 PDTA-Fe 400 Tank 1.2 -0.10 B D E(Comparison) solution .times. 1.19-8 PDTA-Fe 200 Tank 1.4 -0.15 B E E(Comparison) solution .times. 1.29-9 PDTA-Fe 100 Tank 1.8 -0.20 C E E(Comparison) solution .times. 1.49-10 PDTA-Fe 50 Tank 2.1 -0.21 C E E(Comparison) solution .times. 1.89-11 PDTA-Fe 25 Tank 2.2 -0.21 C E E(Comparison) solution .times. 2.69-12 PDTA-Fe 15 Tank 2.2 -0.24 C E E(Comparison) solution .times. 3.09-13 DTPA-Fe 400 Tank 0.0 0.0 C A A(Comparison) solution .times. 1.19-14 DTPA-Fe 200 Tank 0.3 -0.03 D A A(Comparison) solution .times. 1.29-15 DTPA-Fe 100 Tank 0.9 -0.17 E A B(Comparison) solution .times. 1.49-16 DTPA-Fe 50 Tank 1.4 -0.23 E B B(Comparison) solution .times. 1.89-17 DTPA-Fe 25 Tank 1.6 -0.27 E B B(Comparison) solution .times. 2.69-18 DTPA-Fe 15 Tank 1.9 -0.28 E B C(Comparison) solution .times. 3.09-19 A-II-1 400 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.19-20 A-II-1 200 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.2__________________________________________________________________________
TABLE 11__________________________________________________________________________ Organic Amount of Formation of Acid Ferric Bleach-fixer Bleach-fixing Residual SulfidesExperiment Complex Replenisning Replenisher Silver Recoloring Edge Tank Repleni-No. Salt Rate (ml/m.sup.2) Concentration (mg/100 cm.sup.2) Property Effect Solution sher__________________________________________________________________________9-21 A-II-1 100 Tank 0.0 0.0 A A A(Invention) solution .times. 1.49-22 A-II-1 50 Tank 0.0 0.0 A A A(Invention) solution .times. 1.89-23 A-II-1 25 Tank 0.0 0.0 A A B(Invention) solution .times. 2.69-24 A-II-1 15 Tank 0.2 -0.05 B B B(Invention) solution .times. 3.09-25 A-II-3 400 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.19-26 A-II-3 200 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.29-27 A-II-3 100 Tank 0.0 0.0 A A A(Invention) solution .times. 1.49-28 A-II-3 50 Tank 0.0 0.0 A A A(Invention) solution .times. 1.89-29 A-II-3 25 Tank 0.0 0.0 A A B(Invention) solution .times. 2.69-30 A-II-3 15 Tank 0.3 -0.08 B B B(Invention) solution .times. 3.09-31 A-II-15 400 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.19-32 A-II-15 200 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.29-33 A-II-15 100 Tank 0.0 0.0 A A A(Invention) solution .times. 1.49-34 A-II-15 50 Tank 0.0 0.0 A A A(Invention) solution .times. 1.89-35 A-II-15 25 Tank 0.0 -0.03 A A B(Invention) solution .times. 2.69-36 A-II-15 15 Tank 0.4 -0.10 B B B(Invention) solution .times. 3.09-37 A-III-1 400 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.19-38 A-III-1 200 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.29-39 A-III-1 100 Tank 0.0 0.0 A A B(Invention) solution .times. 1.49-40 A-III-1 50 Tank 0.1 -0.03 A B B(Invention) solution .times. 1.8__________________________________________________________________________
TABLE 12__________________________________________________________________________ Organic Amount of Formation of Acid Ferric Bleach-fixer Bleach-fixing Residual SulfidesExperiment Complex Replenisning Replenisher Silver Recoloring Edge Tank Repleni-No. Salt Rate (ml/m.sup.2) Concentration (mg/100 cm.sup.2) Property Effect Solution sher__________________________________________________________________________9-41 A-III-1 25 Tank 0.3 -0.08 A B B(Invention) solution .times. 2.69-42 A-III-1 15 Tank 0.5 -0.15 B B C(Invention) solution .times. 3.09-43 A-III-2 400 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.19-44 A-III-2 200 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.29-45 A-III-2 100 Tank 0.0 0.0 A A B(Invention) solution .times. 1.49-46 A-III-2 50 Tank 0.2 -0.05 A B B(Invention) solution .times. 1.89-47 A-III-2 25 Tank 0.6 -0.10 A B B(Invention) solution .times. 2.69-48 A-III-2 15 Tank 0.7 -0.17 B B C(Invention) solution .times. 3.09-49 A-III-6 400 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.19-50 A-III-6 200 Tank 0.0 0.0 A A A(Comparison) solution .times. 1.29-51 A-III-6 100 Tank 0.0 0.0 A A B(Invention) solution .times. 1.49-52 A-III-6 50 Tank 0.2 -0.05 A B B(Invention) solution .times. 1.89-53 A-III-6 25 Tank 0.4 -0.12 A B B(Invention) solution .times. 2.69-54 A-III-6 15 Tank 0.6 -0.17 B B C(Invention) solution .times. 3.09-55 A-III-21 400 Tank 0.0 0.0 A A A(comparison) solution .times. 1.19-56 A-III-21 200 Tank 0.0 0.0 A A A(comparison) solution .times. 1.29-57 A-III-21 100 Tank 0.0 0.0 A A B(Invention) solution .times. 1.49-58 A-III-21 50 Tank Solution 0.2 -0.06 A B B(Invention) solution .times. 1.89-59 A-III-21 25 Tank 0.6 -0.14 A B B(Invention) solution .times. 2.69-60 A-III-21 15 Tank 0.8 -0.15 B B C(Invention) solution .times. 3.0__________________________________________________________________________
As is apparent from Tables 10 to 12, use of the organic acid ferric complex salt of the invention lessens the amount of residual silver, minimizes edge stains and raises the preservability of a bleach-fixer, even when the replenishing rate of bleach-fixer is reduced.
The bleach and bleach-fixer according to this inventive method for processing silver halide color photographic light-sensitive materials is high in biodegradability, less in amount of waste liquids, and thereby excellent in environmental compatibility. Further, this inventive processing method provides high-quality images less in edge staining and free from bleach fogging, besides its capability of providing a processing solution with stable processing activities.

Number	Date	Country
3-358335	Dec 1991	JPX
4-006625	Jan 1992	JPX
4-028183	Feb 1992	JPX

Number	Name	Date
2322027	Jelley et al.	Dec 1940
2533514	Sawdey et al.	Nov 1947
2767172	Katz et al.	Oct 1956
2767173	Katz	Oct 1956
2767174	Katz et al.	Oct 1956
2870015	Allen et al.	Jan 1959
3370952	Dawson	Feb 1968
3490911	Burness et al.	Jan 1970
3689271	Nittel et al.	Sep 1972
3725067	Bailey et al.	Apr 1973
3764336	Nittel et al.	Oct 1973
3765897	Nittel	Oct 1973
4014764	Seiler et al.	Mar 1977
4036715	Baden et al.	Jul 1977
4065313	Shippey	Dec 1977
4080211	Van Paesschen et al.	Mar 1978
4804618	Ueda et al.	Feb 1989
5149618	Tappe et al.	Sep 1992
5232822	Ishikawa et al.	Aug 1993
5234801	Ishikawa	Aug 1993
5238791	Tappe et al.	Aug 1993
5342740	Goto et al.	Aug 1994
5352567	Okada et al.	Oct 1994

Number	Date	Country
0329088	Aug 1989	EPX
0369999	Nov 1990	EPX
0430000	Jun 1991	EPX
0450293	Oct 1991	EPX
0532003	Mar 1993	EPX

Method of bleaching silver halide color photographic light-sensitive materials using particular ferric chelates

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Entry
Kostromina et al., "Stimulation of Seed, Sugar and Nectar Production of Lucerne by Fertilizing with Ferric-Chelated Ethylenediaminedisuccinic acid".
Aqueous Paste "As Ukr. Gen. Inorg. Chem," Derwent abstract #84-145630.
Ueno, "Chelate Chemistry", vol. 5, Sect. 1, pp. 309, 311, 324 (translation).
"New Complexanes, VIII. Ethylenediamine-N,N'-disuccinic acid and investigation of its heavy metal complexes by spectrophotometry". J. Major et al.
Chem. Zvesti 20 (6), pp. 414-422 (Chem. Abs., vol. 65, 1966, abstract No. 11737f).
"Stereospectric Ligands and their Complexes I. A Cobalt (III) Complex of Ethylenediamine disuccinic Acid", J. Neal et al. Inorg. Chem., Nov. 1968, p. 2405.