Classifications

• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
  • G03C1/00—Photosensitive materials
  • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
  • G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
  • G03C1/061—Hydrazine compounds
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
  • G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
  • G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
  • G03C5/29—Development processes or agents therefor
  • G03C5/30—Developers
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
  • G03C1/00—Photosensitive materials
  • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
  • G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
  • G03C1/08—Sensitivity-increasing substances
  • G03C1/10—Organic substances
  • G03C2001/108—Nucleation accelerating compound

Definitions

• the present invention relates to an image-forming process for providing a ultrahigh contrast with a silver halide photographic material, more particularly, to an image-forming process which is capable of forming ultrahard image with a developing solution containing no dihydroxybenzene series developing agent.
• an image-forming system showing a ultrahard (in particular, gamma ( ⁇ ) is 10 or more) photographic characteristic is required.
• a lithographic developing system utilizing a so-called "infectious development effect" has been used from the past as a method for obtaining a photographic characteristic of a high contrast but it has a defect that a developing solution is instable and difficult to use.
• a method. for obtaining it with a more stable developing solution includes the methods described in U.S. Pat. Nos. 4,224,401, 4,168,977, 4,166,742, 4,311,781, 4,272,606, 4,221,857, 4,332,878, 4,634,661, 4,618,574, 4,269,922, 5,650,746, and 4,681,836.
• the image-forming system is a system in which a silver halide photographic material of a surface latent image type containing a hydrazine derivative is processed in a stable MQ developing solution of pH 11 to 12.3 (an MQ developing solution means a developing solution using hydroquinone and p-aminophenol in combination) or a PQ developing solution (which means a developing solution using hydroquinone and 1-phenyl-3-pyrazolidones in combination) to obtain a ultrahard negative image having ⁇ exceeding 10.
• an MQ developing solution means a developing solution using hydroquinone and p-aminophenol in combination
• a PQ developing solution which means a developing solution using hydroquinone and 1-phenyl-3-pyrazolidones in combination
• a photographic characteristic of a ultrahard contrast and a high sensitivity can be obtained and sulfite of a high concentration is allowed to add to a developing solution. Accordingly, a stability of the developing solution against air oxidation is improved with great strides as compared with a conventional lithographic developing solution.
• JP-A-62-640 the term "JP-A" as used herein means an unexamined published Japanese patent application
• JP-A-62-235938 the term "JP-A-62-235939”
• JP-A-63-10404 JP-A-63-103235
• JP-A-63-296031 JP-A-63-314541
• JP-A-64-13545 JP-A-62-640
• Patent T896,022 and JP-B-46939 (the term "JP-B" as used herein means an examined Japanese patent publication) but an effect for an increased contrast is scarcely found while a development accelerating effect is seen.
• An effect for a combined use of ascorbic acid and a quaternary salt is described as well in JP-A-3-249756 and 4-32838 but a contrast of an image obtained is not sufficient.
• JP-A-5-88306 that a high contrast can be obtained by using ascorbic acid as a sole developing agent and maintaining pH to 12.0 or higher but a problem is involved in a stability of the developing solution.
• a ultrahard image-forming system using a hydrazine derivative is a system using a dihydroxybenzene compound such as hydroquinone as a developing agent as described above and has several disadvantages from ecological and toxicological points of view.
• hydroquinone is an undesirable component because of an allergic disadvantages
• 1-phenyl-3-pyrazolidones are a component having an inferior biodegradation.
• sulfite of a high concentration shows a high COD (chemical oxygen demand).
• amines described in U.S. Pat. No. 4,975,354 are usually used in combination but not preferred in terms of a toxicity and a volatility.
• the object of the present invention is to provide a novel image-forming process which makes it possible to obtain a high contrast image required in a graphic art field by using a developing solution having no problem against an ecological system and a working environment.
• the objects of the present invention have been achieved by an image-forming process in which a photographic material having at least one silver halide emulsion layer on a support and containing a hydrazine compound in the above emulsion layer or the other constitutional layers, is subjected to a development processing in a developing solution after exposing, wherein the above hydrazine compound is represented by the following formula (I); the above developing solution contains a developing agent represented by the following formula (II) and does not substantially contain a dihydroxybenzene developing agent: ##STR2## wherein R 1 represents an aliphatic group or an aromatic group; R 2 represents a hydrogen atom, an alkyl group, an aryl group, an unsaturated heterocyclic group, an alkoxy group, an aryloxy group, an amino group, a hydrazinc group, a carbamoyl group, or an oxycarbonyl group; G 1 represents --CO--, --SO 2 --, --SO--, ##STR3## --CO-
• the aliphatic group represented by R 1 has preferably 1 to 30 carbon atoms and particularly is a linear, branched or cyclic alkyl group having 1 to 20 carbon atoms, wherein the branched alkyl group may be cyclized so that a saturated heterocyclic group containing therein one or more hetero atoms is formed; and this alkyl group may have a substituent such as an alkyl group, an aryl group, an alkoxy group, a sulfoxy group, a sulfonamide group, and a carbonamide group.
• the aromatic group represented by R 1 is a monocyclic or dicyclic aryl group or an unsaturated heterocyclic group, wherein the unsaturated heterocyclic group may be condensed with a monocyclic or dicyclic aryl group to form a heteroaryl group. It includes, for example, a benzene ring, a naphthalene ring, a pyridine ring, a pyrimidine ring, an imidazole ring, a pyrazole ring, a quinoline ring, an isoquinoline ring, a benzimidazole ring, a thiazole ring, and a benzothiazole ring. Of them, that containing a benzene ring is preferred.
• R 1 is an aryl group.
• the aryl group or the unsaturated heterocyclic group of R 1 may be substituted.
• Example of the representative substituent includes, for example, an alkyl group, an aralkyl group, an alkenyl group, an alkynyl group, an alkoxy group, an aryl group, a substituted amino group, a ureido group, a urethane group, an aryloxy group, a sulfamoyl group, a carbamoyl group, an alkyl- or arylthio group, an alkyl- or arylsulfonyl group, an alkyl- or arylsulfinyl group, a hydroxy group, a halogen atom, a cyano group, a sulfo group, an aryloxycarbonyl group, an acyl group, an alkoxycarbonyl group, an acyloxy group, a carbonamide group, a sulfonamide group,
• the preferred substituents include a linear, branched or cyclic alkyl group (preferably that having 1 to 20 carbon atoms), an aralkyl group (preferably a monocyclic or dicyclic one having 1 to 3 carbon atoms in an alkyl portion), an alkoxy group (preferably that having 1 to 20 carbon atoms), a substituted amino group (preferably an amino group substituted with an alkyl group having 1 to 20 carbon atoms), an acylamino group (preferably that having 2 to 30 carbon atoms), a sulfonamide group (preferably that having 1 to 30 carbon atoms), a ureido group (preferably that having 1 to 30 carbon atoms), and a phosphoric amide group (preferably that having 1 to 30 carbon atoms).
• a linear, branched or cyclic alkyl group preferably that having 1 to 20 carbon atoms
• an aralkyl group preferably a monocyclic or dicyclic one having 1 to 3 carbon atoms in an alky
• R 1 is an aryl group and the substituent therefor is an arylsulfonamide group
• a group in which a group substituted to an aryl group of the arylsulfonamide group contains three or more --CH 2 --CH 2 O-- units in the structure thereof, or a group containing a pyridinium group.
• the alkyl group represented by R 2 is preferably an alkyl group having 1 to 4 carbon atoms and may have a substituent such as a halogen atom, a hydroxyl group, a cyano group, a carboxy group, a sulfo group, an alkoxy group, a phenyl group, an acyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, a carbamoyl group, an alkyl- or arylsulfonyl group, a sulfamoyl group, a nitro group, a heteroaromacyclic group, and a R 1 --NA 1 --NA 2 --G 1 -- group.
• substituent groups may further be substituted.
• a monocyclic or dicyclic aryl group is preferred as the aryl group, and it is, for example, that containing a benzene ring.
• This aryl group may be substituted and the examples of the substituent are the same ones as the case of the alkyl group.
• the unsaturated heterocyclic group is a 5- to 6-membered unsaturated heterocyclic group containing at least one of a nitrogen atom, an oxygen atom and a sulfur atom in the ring, which includes, for example, an imidazolyl group, a pyrazolyl group, a triazolyl group, a tetrazolyl group, a pyridyl group, a pyridinium group, a quinolium group, and a quinolinyl group.
• the pyridyl group or the pyridinium group is particularly preferred.
• alkoxy group having 1 to 8 carbon atoms is preferred as the alkoxy group and may be substituted with a halogen atom and an aryl group.
• a monocyclic group is preferred as the aryloxy group and a substituent includes a halogen atom.
• amino group are a non-substituted amino group, an alkylamino group having 1 to 10 carbon atoms, and an arylamino group and may be substituted with an alkyl group, a halogen atom, a cyano group, a nitro group, and a carboxy group.
• the carbamoyl group are a non-substituted carbamoyl group, an alkylcarbamoyl group having 1 to 10 carbon atoms, and an arylcarbamoyl group and may be substituted with an alkyl group, a halogen atom, a cyano group, and a carboxy group.
• oxycarbonyl group are an alkoxycarbonyl group having 1 to 10 carbon atoms, and an aryloxycarbonyl group and may be substituted with an alkyl group, a halogen atom, a cyano group, and a nitro group.
• G 1 is --CO--
• R 2 of the groups represented by R 2 , preferred is a hydrogen atom, an alkyl group (for example, methyl, trifluoromethyl, 3-hydroxypropyl, 3-methanesulfonamidepropyl, and phenylsulfonylmethyl), an aralkyl group (for example, o-hydroxybenzyl), or an aryl group (for example, phenyl, 3,5-dichlorophenyl, o-methanesulfonamidephenyl, 4-methanesulfonylphenyl, and 2-hydroxymethylphenyl).
• a hydrogen atom is particularly preferred.
• R 2 is preferably an alkyl group (for example, methyl), an aralkyl group (for example, o-hydroxybenzyl), an aryl group (for example, phenyl), or a substituted amino group (for example, dimethylamino).
• preferred R 2 includes a cyanobenzyl group and a methylthiobenzyl group
• R 2 is preferably methoxy, ethoxy, butoxy, phenoxy, or phenyl. In particular, phenoxy is suitable.
• G 1 is an N-substituted or non-substituted iminomethylene group
• preferred R 2 is methyl, ethyl, or substituted or non-substituted phenyl.
• the substituents for R 1 can be applied as well to the substituents for R 2 .
• a --CO-- group is most preferred as G in formula (I).
• R 2 may be a portion of G 1 -R 2 to split off from a residual part and may cause a cyclization reaction by which a cyclic structure containing the atoms in the portion of --G 1 --R 2 is formed.
• R 2 may be represented by formula (a):
• Z 1 is a group which can nucleophilically attack G 1 to split a G 1 -R 3 -Z 1 portion off from a residue of the molecule; and R 3 is obtained by removing one hydrogen atom from R 2 and nucleophilically attacks G 1 to make G 1 , R 3 and Z 1 possible to form a cyclic structure.
• G 1 such as OH, SH, N
• R b1 to R b4 each represents a hydrogen atom, an alkyl group (preferably that having 1 to 12 carbon atoms), an alkenyl group (preferably that having 2 to 12 carbon atoms), or an aryl group (preferably that having 6 to 12 carbon atoms), and it may be the same or different;
• B is the atoms necessary to complete a 5- or 6-membered ring which may have a substituent; and m and n each are 0 or 1 and (n+m) is 1 or 2.
• the 5- or 6-membered ring formed by B in formula (b) includes, for example, a cyclohexene ring, a cyclopentene ring, a benzene ring, a naphthalene ring, a pyridine ring, and a quinoline ring.
• Z 1 is the same as that in formula (a).
• R c1 and R c2 each represents a hydrogen atom, an alkyl group, an alkenyl group, an aryl group, or a halogen atom and may be the same or different;
• R c3 represents a hydrogen atom, an alkyl group, an alkenyl group, or an aryl group; and
• p represents an integer of 0 to 2 and q represents 1 to 4.
• R c1 , R c2 and R c3 may be combined with each other to form a ring as long as Z 1 is of a structure in which Z 1 may be an intermolecular nucleophilic attack to C 1 .
• R c1 and R c2 each are preferably a hydrogen atom, a halogen atom, or an alkyl group
• R c3 is preferably an alkyl group or an aryl group.
• q represents preferably 1 to 3.
• p represents 1 or 2 when q is 1, 0 or 1 when q is 2, and 0 or 1 when q is 3.
• q is 2 or 3
• Z 1 represents the same as that in formula (a).
• a 1 and A 2 each is a hydrogen atom, an alkylsulfonyl or arylsulfonyl group having 20 or less carbon atoms (preferably phenylsulfonyl or phenylsulfonyl which is substituted so that a sum of a Hammett's substituent constant becomes -0.5 or more), an acyl group having 20 or less carbon atoms (preferably benzoyl or benzoyl which is substituted so that a sum of a Hammett's Substitution Constant may be -0.5 or more), or a linear, branched or cyclic, non-substituted and substituted aliphatic acyl group (a substituent includes a halogen atom, an ether group, a sulfonamide group, a carbonamide group, a hydroxyl group, a carboxy group, and a sulfonic acid group).
• a hydrogen atom is the most preferred as A 1 and A 2 .
• R 1 or R 2 in formula (I) may have a ballast group or polymer incorporated thereinto, which is conventionally used for an immobile photographic additive such as a coupler.
• the ballast group having 8 or more carbon atoms is comparatively inactive to the photographic characteristics, and is selected from, for example, an alkyl group, an alkoxy group, a phenyl group, an alkylphenyl group, a phenoxy group, and an alkylphenoxy group.
• the polymer described in JP-A-l-100530 may also be used.
• R 1 or R 2 in formula (I) may incorporates a group for strengthening an adsorption to a surface of a silver halide grain.
• the adsorbing group include a thiourea group, a heterocyclic thioamide group, a mercapto heterocyclic group, and a triazole group, which are described in U.S. Pat. Nos.
• hydrazine compound represented by formula (I) having a ballast group, an immobile group such as a polymer group, or a group enhancing adsorption property to a surface of a silver halide grain into R 1 or R 2 described above, or the hydrazine compound represented by the following formula (X):
• L 11 represents a single bond, --O--, --S--, --NR 16 --, --CO, --SO 12 --, --P(O)(G 12 R 16 )-, or the combination thereof;
• L 12 represents --SO 2 NR 16 --, --NR 16 SO 2 NR 16 --, --CONR 16 --, --NR 16 CONR 16 --, or --G 12 P(O)(G 12 R 16 )NR 16 -, in which G 12 represents a single bond, --O--, or --NR 16 --, wherein R 16 represents a hydrogen atom, an aliphatic group, or an aromatic group;
• G 11 is the same as G in formula (I), and R 15 is the same as R 2 in formula (I);
• R 11 represents an aliphatic group or an aromatic group (three R 11 's may be the same or different), and
• R 12 , R 13 and R 14 each represents a divalent aliphatic group or aromatic group;
• m is 0 or 1
• X - represents a
• the aliphatic group represented by R 11 has preferably 1 to 30 carbon-atoms and is particularly a linear, branched or cyclic alkyl group having 1 to 20 carbon atoms.
• the aromatic group represented by R 11 is a monocyclic or dicyclic aryl group or and an unsaturated heterocyclic group, wherein the unsaturated heterocyclic group may be condensed with an aryl group.
• the aliphatic group or the aromatic group of R 1 may be substituted and examples of the substituents include, for example, an alkyl group, an aralkyl group, an alkenyl group, an alkynyl group, an alkoxy group, an aryl group, a substituted amino group, a ureido group, a urethane group, an aryloxy group, a sulfamoyl group, a carbamoyl group, an alkyl- or arylthio group, an alkyl- or arylsulfonyl group, an alkyl- or arylsulfinyl group, a hydroxy group, a halogen atom, a cyano group, a sulfo group, an aryloxycarbonyl group, an acyl group, an alkoxycarbonyl group, an acyloxy group, a carbonamide group, a sulfonamide group, a carboxyl group,
• the preferred substituents include an alkyl group (preferably having 1 to 20 carbon atoms), an aralkyl group (preferably having 7 to 30 carbon atoms), an alkoxy group (preferably having 1 to 20 carbon atoms), a substituted amino group (preferably an amino group substituted with an alkyl group having 1 to 20 carbon atoms), an acylamino group (preferably having 2 to 30 carbon atoms), a sulfonamide group (preferably having 1 to 30 carbon atoms), a ureido group (preferably having 1 to 30 carbon atoms), and a phosphoric amide group (preferably having 1 to 30 carbon atoms). These groups may further be substituted.
• R 11 's in formula (X) may be the same or different and may be combined with each other to form a ring.
• the aliphatic group represented by R 12 , R 13 and R 14 preferably has 1 to 30 carbon atoms, particularly a linear, branched or cyclic alkyl group having 1 to 20 carbon atoms.
• the aromatic group represented by R 12 , R 13 and R 14 is a monocyclic or dicyclic aryl group or an unsaturated heterocyclic group, wherein the unsaturated heterocyclic group may be condensed with an aryl group.
• R 12 is an alkyl group having 1 to 10 carbon atoms
• R 13 and R 14 is an aryl group, particularly preferably contains a benzene ring.
• the aliphatic group or the aromatic group of R 12 , R 13 and R 14 may be substituted, and those enumerated as the substituent for R 11 can be applied as the representative substituent therefor.
• L 11 represents a single bond, a --O--group, a --S- group, a --NR 16 --group, a --CO- group, a --SO 12 --group, a -P(O)(G 12 R 16 )--group, or the combination thereof and represents preferably a --SO 2 NR 16 --group, a --NR 16 SO 12 NR 16 --group, a --CONR 16 -group, a --NR 16 CONR 16 --group, or a --G 12 P(O)(G 12 R 16 )NR 16 --group, particularly preferably represents --CONR 16 --.
• R 6 is preferably a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, particularly preferably a hydrogen atom.
• R 11 , R 12 , R 13 , R 14 or R 15 in formula (X) may have a ballast group or polymer incorporated therein, which is conventionally used for an immobile photographic additive such as a coupler.
• the ballast group having 8 or more carbon atoms is relatively inactive to the photographic characteristics, and can be selected from, for example, an alkyl group, an alkoxy group, a phenyl group, an alkylphenyl group, a phenoxy group, and an alkylphenoxy group.
• the compounds described in JP-A-1-100530 can be used as the polymer.
• R 11 , R 12 , R 13 , R 14 or R 15 in formula (X) may be incorporated into a group enhancing adsorption property to a surface of a silver halide grain.
• Examples of the adsorbing group include a thiourea group, a heterocyclic thioamide group, a mercapto heterocyclic group, and a triazole group which are described in U.S. Pat. Nos. 4,385,108 and 4,459,347, JP-A-59-195,233, JP-A-59-200,231, JP-A-59-201,045, JP-A-59-201,046, JP-A-59-201,047, JP-A-59-201,048, JP-A-59-201,049, JP-A-61-170,733, JP-A-61-270,744, JP-A-62-948, JP-A-63-234,244, JP-A-63-234,245, and JP-A-63-234,246.
• the hydrazine derivative used in the present invention includes those described in Research Disclosure Item 23516 (November 1983, pp. 346) and the publications cited therein, and in addition, U.S. Pat. Nos. 4,080,207, 4,269,929, 4,276,364, 4,278,748, 4,385,108, 4,459,347, 4,560,638, and 4,478,928, British Patent 2,011,391B, JP-A-60-179,734, JP-A-62-270,948, JP-A-63-29,751, JP-A-61-170,733, JP-A-61-270,744, JP-A-62-948, EP 217,310, or U.S. Pat.
• An addition amount of the hydrazine derivative used in the present invention is preferably 1 ⁇ 10 -6 to 5 ⁇ 10 -2 mole per mole of silver halide, and in particularly, preferred within a range of 1 ⁇ 10 -5 to 2 ⁇ 10 -2 mole per mole of silver halide.
• the hydrazine derivatives used in the present invention may be dissolved in a suitable solvent, for example, alcohols (methanol, ethanol, propanol, and fluorinated alcohol), ketones (acetone and methyl ethyl ketone), dimethylformamide, dimethylsulfoxide, and methyl cellosolve.
• a suitable solvent for example, alcohols (methanol, ethanol, propanol, and fluorinated alcohol), ketones (acetone and methyl ethyl ketone), dimethylformamide, dimethylsulfoxide, and methyl cellosolve.
• the hydrazine derivatives may be dissolved with an aid of an oil such as dibutyl phthalate, tricresyl phosphate, glyceryl triacetate, and diethyl phthalate, and an auxiliary solvent such as ethyl acetate and cyclohexanone to mechanically disperse the emulsified solution thereof by the well known dispersing methods as well.
• an oil such as dibutyl phthalate, tricresyl phosphate, glyceryl triacetate, and diethyl phthalate
• an auxiliary solvent such as ethyl acetate and cyclohexanone
• the powders of the hydrazine derivatives can be dispersed in water by a known solid dispersing method in a ball mill, a colloid mill or a supersonic wave as well.
• a nucleation accelerator such as an amine derivative, an onium salt, a disulfide derivative, and a hydroxylamine derivative is preferably added to a silver halide emulsion layer and the other hydrophilic colloid layers in the silver halide photographic material of the present invention.
• nucleation accelerator examples include an amine derivative, an onium salt, a disulfide derivative, and a hydroxylamine derivative.
• the compounds described in JP-A-60-140,340, JP-A-62-50,829, JP-A-62-222,241,JP-A-62-250,349, JP-A-62-280,733, JP-A-63-124,045, JP-A-63-133,145, and JP-A-63-286,840 may be used, and more preferably the compounds having a group adsorbing property to silver halide, described in JP-A-63-124,045, JP-A-63-133,145 and JP-A-63-286,840, the compounds having a total carbon atom of 20 or more, described in JP-A-62- 222,241, and the amine compounds having an ethylene group, described in U.S. Pat. No. 4,975,354 and EP 458P706A, and the compounds described in JP-A-62-50829 may be used.
• a pyridinium salt, an ammonium salt or a phosphonium salt is preferred as the onium salt.
• the compounds described in Japanese patent application No. 5-97866 can be used as an example of the preferred pyridinium salt.
• the compounds described in JP-A-62-250,439 and JP-A-62-280,733 can be used as an example of the preferred ammonium salt.
• the compounds described in JP-A-61-167,939 and JP-A-62-280,733 can be used as an example of the preferred phosphonium salt.
• Example of the hydroxymethyl derivative includes the compounds described in, for example, U.S. Pat. Nos. 4,698,956 and 4,777,118, EP 231,850, and JP-A-62-50,829, more preferably a diaryl methacrynol derivative.
• JP-A-3-168735 and JP-A-2-271351 can be used as the acetylene derivative.
• An optimum additional amount of these compounds may be varied depending on the kind thereof, and is used desirably in a range of 1.0 ⁇ 10 -2 to 1.0 ⁇ 10 -2 mole, preferably 1.0 ⁇ 10 -2 to 5.0 ⁇ 10 mole per mole of the hydrazine compound.
• Suitable solvent for example, alcohols (methanol, ethanol, propanol, and fluorinated alcohol), ketones (acetone and methyl ethyl ketone), dimethylformamide, dimethylsulfoxide, and methyl cellosolve.
• alcohols methanol, ethanol, propanol, and fluorinated alcohol
• ketones acetone and methyl ethyl ketone
• dimethylformamide dimethylsulfoxide
• methyl cellosolve methyl cellosolve
• the hydrazine derivatives can be dissolved with an aid of an oil such as dibutyl phthalate, tricresyl phosphate, glyceryl triacetate, and diethyl phthalate, and an auxiliary solvent such as ethyl acetate and cyclohexanone to mechanically disperse the emulsified solution thereof by the well known dispersing methods as well.
• an oil such as dibutyl phthalate, tricresyl phosphate, glyceryl triacetate, and diethyl phthalate
• an auxiliary solvent such as ethyl acetate and cyclohexanone
• the powders of these compounds can be dispersed in water by a known solid dispersing method in a ball mill, a colloid mill or a supersonic wave as well.
• halogen composition of the silver halide emulsion used in the present invention suitable of which are selected from silver chloride, silver chlorobromide, silver chloroiodobromide, and silver iodobromide.
• the silver chloride content thereof is preferably 30 mole % or more.
• Any of one side mixing process, a simultaneous mixing process and the combination thereof may be used as a process for reacting a water soluble silver salt (an aqueous silver nitrate solution) with a water soluble halide.
• a simultaneous mixing process in which pAg in the solution for forming silver halide, is maintained constant, that is, the process called as a controlled double jet process may be used.
• a so-called silver halide solvent such as ammonia, thioether, and tetra-substituted thiourea, is preferably used to form a grain.
• a tetra-substituted thiourea compound is more preferable and is described in JP-A-53-82408 and JP-A-55-77737.
• Preferred thiourea compound is tetramethyl thiourea or 1,3-dimethyl-2-imidazolidinethione.
• a silver halide emulsion having a regular crystal form and a narrow grain size distribution can readily be prepared by the controlled double jet process and a grain forming process using a silver halide solvent, and said processes are the useful means for preparing the emulsion according to the present invention.
• Silver halide contained in the photographic emulsion used in the present invention has an average grain size of 0.5 ⁇ m or less, particularly preferably 0.1 to 0.4 ⁇ m.
• the silver halide grains may have a relatively broad size distribution but have preferably a narrow size distribution.
• the sizes of the grains sharing 90% of the total in terms of a weight or a number reside within ⁇ 40% of an average grain size.
• such an emulsion is defined as a monodispersed emulsion.
• the silver halide grains contained in a photographic emulsion may have a regular crystal form such as cubic, octahedron, or a spherical silver halide grains or tabular silver halide grains having a high aspect ratio described in Research Disclosure No. 22534 (Jan. 1983). Further, they may be those having the composite form of these crystal habits.
• the silver halide grains may be composed of either an uniform layer or distinctive layers in an inside and a surface thereof. Two or more kinds of the silver halide emulsions such as the inner latent image type and the surface latent image type silver halide emulsion grains, each described in JP-B-41-2068, separately prepared may be mixed and used.
• a cadmium salt, sulfite a lead salt, a thallium salt, a rhodium salt or the complex salt thereof, and an iridium salt or the complex salt thereof may coexist with the silver halide emulsion in a process of a forming or a physical ripening the silver halide grains.
• a silver halide emulsion particularly suitable for the light-sensitive materials for photographic line drawing and preparing a halftone dot is an emulsion prepared in the presence of the iridium salt or the complex salt thereof of 10 -8 to 10 -5 mole per mole of silver.
• the above amount of the iridium salt is preferably added before finishing a physical ripening in a manufacturing process of a silver halide emulsion, particularly in a grain formation.
• the iridium salt used herein is a water soluble iridium salt or an iridium complex salt and includes, for example, iridium trichloride, iridium tetrachloride, potassium hexachloroiridate (III), potassium hexachloro-iridate (IV), and ammonium hexachloroiridate (III).
• a so-called non-post ripening emulsion (a primitive emulsion) which is not subjected to a chemical sensitization can be used as a silver halide emulsion but may be subjected to the chemical sensitization.
• chemical sensitization a process described in H. Frieser, "Die Grundlagen der Photographischen Sawe mit Silver Halogeniden” Akademische Verlagsgesselschaft, (1968).
• a sulfur sensitizing process using active gelatin and a compound containing sulfur capable of reacting with silver for example, thiosulfate, thioureas, a mercapto compound, and rhodanines
• a reduction sensitizing process using a reductive compound for example, a stannous salt, amines, a hydrazine derivative, formamidinesulfinic acid, and a silane compound
• a noble metal sensitizing process using a noble metal compound for example, in addition to a gold compound, a complex salt of the VIII group metal in the Periodic Table, such as platinum, iridium, and palladium.
• the preferred chemical sensitizing process is a gold sulfur sensitizing process.
• the silver halide emulsion of the present invention contains preferably complex, of a transit ion metal such as Rh, Ru, Re, Os, Ir, and Cr.
• a ligand As a ligand, nitrosyl and thionitrosyl crosslinking ligands, a halide ligand (fluoride, chloride, bromide and iodide), a cyanide ligand, a cyanate ligand, a thiocyanate ligand, a selenocyanate ligand, a tellurocyanate ligand, an acid ligand, and an aquo ligand may be used. In the case where the aquo ligand is present, it occupies preferably one or two of the ligands.
• a rhodium atom can be converted to an arbitrary form of a metal salt such as a single salt and a complex salt to add it in the preparation of the grains.
• Example of the rhodium salt includes rhodium monochloride, rhodium dichloride, rhodium trichloride, and ammonium hexachlororhodate.
• Preferred is a water soluble trivalent.
• rhodium complex compound for example, hydrogen hexachlororhodate (III) or the salt thereof (an ammonium salt, a sodium salt and a potassium salt).
• rhodium salts are used in an addition amount in a range of 1.0 ⁇ 10 -6 to 1.0 ⁇ 10 -3 mole, preferably 1.0 ⁇ 10 -5 to 1.0 ⁇ 10 -3 mole, and particularly preferably 5.0 ⁇ 10 -5 to 5.0 ⁇ 10 -4 mole per mole of silver halide.
• the light-sensitive silver halide emulsion according to the present invention may be spectrally sensitized to a blue light having a relatively long wavelength, a green light, a red light, or an infrared ray by a sensitizing dye.
• a sensitizing dye includes a cyanine dye, a merocynine dye, a complex cyanine dye, a complex meroyanine dye, a holopolar cyanine dye, a styryl dye, a hemicyanine dye, an oxonol dye, and a hemioxonol dye.
• sensitizing dyes may be used either singly or in combination thereof.
• the combination of the sensitizing dyes is often used particularly for the purpose of a supersensitization.
• a water soluble dye may be incorporated into a hydrophilic colloid layer in the photographic material according to the present invention as a filter dye or for various purposes of an anti-irradiation dye and others.
• Such a dye includes an oxonol dye, a hemioxonol dye, a styryl dye, a merocyanine dye, a cyanine dye, and an azo dye. Of them, useful are the oxonol dye, the hemioxonol dye and the merocyanine dye.
• the examples of the dyes capable of being used are those described in German Patent 616,077, British Patents 584,609 and 1,117,429, JP-B-26-7777, JP-B-39-22069, JP-B-54-38129, JP-A-48-85130, JP-A-49-99620, JP-A-49-114420, JP-A-49-129537, PB Report No. 74175, and Photographic Abstract 128 ('21).
• Gelatin is advantageously used as a binder or protective colloid which can be used in an emulsion layer and an intermediate layer in the light-sensitive material of the present invention, and the other hydrophilic colloids can be used as well.
• proteins such as an albumin, and casein; a gelatin derivative; a graft polymer of gelatin and the other polymers, a cellulose derivative such as hydroxyethyl cellulose, carboxymethyl cellulose and cellulose sulfuric acid esters; a sugar derivative such as sodium alginate and starch; and various synthetic hydrophilic high molecular materials such as homopolymers or copolymers including polyvinyl alcohol, partially acetalized polyvinyl alcohol, poly-N-vinyl-pyrrolidone, polyacrylic acid, polymethacrylic acid, polyacrylamide, polyvinylimidazole, and polyvinylpyrazole may be used.
• Various compounds can be incorporated into the photographic emulsion used in the present invention for a purpose of preventing a fog in manufacturing, during storage or in a photographic processing of the light-sensitive material, or stabilizing a photographic performance. That is, there can be added many compounds known as an anti-fogging agent and a stabilizer, such as azoles, for example, a benzothiazolium salt , nitroimidazoles , nitrobenzimidazoles , chlorobenzimidazoles, bromobenzimidazoles, mercaptothiazoles, mercaptobenzothiazoles , mercaptobenzimidazoles , mercaptothiadiazoles, aminotriazoles, benzothiazoles, nitrobenzotriazoles, and mercaptetrazoles (particularly 1-phenyl-5-mercaptotetrazole ); mercaptopyrimidines; mercaptotriazines; a thioketo compound such as, for example, o
• benzotriazoles for example, 5-methyl-benzotriazole. These compounds may be incorporated as well into a processing solution.
• An inorganic or organic hardener may be incorporated into a photographic emulsion layer and the other hydrophilic colloid layers in the photographic material of the present invention.
• the hardness can be used singly or in combination, for example, a chromium salt (chromium alum and chromium acetate), aldehydes (formaldehyde, glyoxal and glutaraldehyde), an N-methylol compound (dimethylolurea and methyloldimethylhydantoin), a dioxane derivative (2,3-dihydroxydioxane), an active vinyl compound (1,3,5-triacryloyl-hexahydro-s-triazine), and mucohalogenic acids (mucochloric acid and mucophenoxychloric acid).
• a chromium salt chromium alum and chromium acetate
• aldehydes formaldehyde, glyoxal and
• the photographic emulsion layers and other hydrophilic colloid layers of the light-sensitive material prepared according to the present invention may contain various surface active agents for various purposes such a as coating aid, anti-static, improvement in a sliding property, an emulsification-dispersion, anti-sticking, and improvement in the photographic characteristics (for example, development acceleration, harder contrast and sensitization).
• a dispersion of a water insoluble or scarcely soluble synthetic polymer can be incorporated into the photographic material used in the present invention for a purpose of improvement in a dimensional stability.
• a subbing layer which can be used in the present invention includes a subbing processing layer with an organic solvent system containing polyhydroxybenzenes, described in JP-A-49-3972, and an aqueous latex subbing processing layer described in JP-A-49-11118 and JP-A-52-10491.
• the above subbing layers can usually be provided on the surfaces thereof with chemical and physical treatments.
• a surface activation treatment such as a chemicals treatment, a mechanical treatment, and a corona discharge treatment may be used as the above treatment.
• the developing solution of the present invention does not substantially contain a dihydroxybenzene developing agent, and a main developing agent is the compound represented by formula (II).
• auxiliary developing agents preferred in the developing solution of the present invention are a 1-phenyl-3-pyrazolidone auxiliary developing agent and/or a p-aminophenol auxiliary developing agent.
• R 21 and R 22 each represents a hydroxy group, an amino group (including that containing an alkyl group having 1 to 10 carbon atoms as a substituent, for example, methyl, ethyl, n-butyl, and hydroxyethyl), an acylamino group (acetylamino and benzoylamino), an alkylsulfonylamino group (methanesulfonylamino), an arylsulfonylamino group (benzenesulfonylamino and p-toluenesulfonylamino), an alkoxycarbonylamino group (methoxycarbonylamino), a mercapto group, or an alkylthio group (methylthio and ethylthio).
• X represents a carbon atom, an oxygen atom or a nitrogen atom and constitutes a 5- to 6-membered ring in cooperation with two vinyl carbons and a carbonyl carbonon which R 1 and R 2 are substituted.
• An example of X includes --O--, --C(R 23 )(R 24 )--, --C(R 25 ) ⁇ , --C( ⁇ O)--, --N(R 26 )--, and -N ⁇ in combination.
• R 23 , R 24 , R 25 and R 26 each represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms and may be substituted (by a hydroxy group, a carboxy group and a sulfo group as a substituent), an aryl group having 6 to 15 carbon atoms and may be substituted (by an alkyl group, a halogen atom, a hydroxy group, a carboxy group, and a sulfo group as a substituent), a hydroxy group, or a carboxy group.
• this 5- to 6-membered ring may form a saturated or unsaturated condensed ring.
• this 5- to 6-membered ring include a dihydrofuranone ring, a dihydropyrone ring, a pyranone ring, a cyclopentenone ring, a cyclohexenone ring, a pyrrolinone ring, a pyrazolinone ring, a pyridone ring, an azacyclohexenone ring, and a uracil ring, more preferably a dihydrofuranone ring, a cyclopentenone ring, a cyclohexenone ring, a pyrazolinone ring, an azacyclohexenone ring, and a uracil ring.
• Y represents ⁇ O or ⁇ N--R 23 , wherein R 23 represents a hydrogen atom, a hydroxyl group, an alkyl group (for example, methyl and ethyl), an acyl group (for example, acetyl), a hydroxyalkyl group (for example, hydroxymethyl and hydroxyethyl), a sulfoalkyl group (for example, sulfomethyl and sulfoethyl), and a carboxyalkyl group (for example, carboxymethyl and carboxyethyl).
• R 23 represents a hydrogen atom, a hydroxyl group, an alkyl group (for example, methyl and ethyl), an acyl group (for example, acetyl), a hydroxyalkyl group (for example, hydroxymethyl and hydroxyethyl), a sulfoalkyl group (for example, sulfomethyl and sulfoethyl), and
• ascorbic acid or erysorbic acid (optical steromer) is preferred.
• An amount of the compound of formula (II) generally ranges in 5 ⁇ 10 -3 mole to 1 mole, particularly preferably 10 -2 mole to 0.5 mole per liter of a developing solution.
• 1-phenyl-3-pyrazolidone or the derivative thereof as an auxiliary developing agent include 1-phenyl-3-pyrazolidone, 1-phenyl-4,4-dimethyl-3-pyrazolidone, 1-phenyl-4-methyl-4-hydroxymethyl-3-pyrazolidone, 1-phenyl-4,4-dihydroxymethyl-3-pyrazolidone, 1-phenyl-5-methyl-3-pyrazolidone, 1-p-aminophenyl-4,4-dimethyl-3-pyrazolidone, and 1-p-tolyl-4-methyl-4-hydroxymethyl-3-pyrazolidone.
• a p-aminophenol auxiliary developing agent includes N-methyl-p-aminophenol, p-aminophenol, N-( ⁇ -hydroxyethyl)-p-aminophenol, N-(4-hydroxyphenyl)glycine, 2-methy-p-aminophenol, and p-benzylaminophenol. Among them, N-methyl-p-amino-henol is preferred.
• the compound of the present invention represented by formula (II) and 1-phenyl-3-pyrazolidones or p-aminophenols is usually used preferably in an amount of 10 -3 mole/liter to 0.1 mole/liter, more preferably 10 -3 mole/liter to 0.06 mole/liter of the developing solution.
• the term of "containing substantially no dihydroxybenzenes" means that a concentration of dihydroxybenzenes in a developing solution is insignificant (for example, 5 ⁇ 10 -4 mole/liter or less) as compared with the amounts of the compound of formula (II) and the auxiliary developing agents described above.
• the developing solution of the present invention preferably contains no dihydroxybenzenes.
• sulfites such as sodium sulfite, potassium sulfite, lithium sulfite, sodium bisulfite, potassium metabisulfite, and formaldehyde sodium bisulfite.
• Sulfite is used in amount of 0.01 mole/liter or more of the developing solution. Use in lots amount of the sulfite will dissolve a silver halide emulsion grain resulting in causing silver stain. Further, this causes increase in COD (chemical oxygen demand) of the developing solution, and accordingly, an addition amount should be limited to a necessary minimum.
• COD chemical oxygen demand
• a developing solution used in the development processing in the present invention has preferably Ph ranging in 10.0 to 12.0, further preferably 10.4 to 12. If Ph is 12.0 or higher, suddenly increases stain and black spot in a non-image portion and therefore is not preferred. Further, Ph of 10.0 or less does not provide a sufficient contrast.
• An alkali agent used for adjusting Ph includes sodium hydroxide, potassium hydroxide, sodium carbonate, and potassium carbonate.
• JP-A-60-93433 for example, succharose
• oximes for example, acetoxime
• phenols for example, 5-sulfosalicylic acid
• silicate and a Ph buffer agent, such as sodiumtertiary phosphate and potassium tertiary phosphate.
• a concentration of the buffer agent is preferably 0.3 mole/liter or more of the developing solution.
• a boron compound such as boric acid and sodium metaborate is not preferred since it is liable to react with the compound of the present invention to inactivate thereof.
• a development inhibitor such as potassiumbromide and potassium iodide
• an organic solvent such as ethylene glycol, diethylene glycol, triethylene glycol, dimethylformamide, methyl cellosolve, hexylene glycol, ethanol, and methanol
• an anti-fogging agent including an indazole compound such as 5-nitoindazole, a benzimidazole compound such as sodium 2-mercaptobenzimidazole-5-sulfonate, a benzotriazole compound such as 5-methylbenzotriazole, and there may be contained the development accelerators described in Research Disclosure Vol. 176, No. 17643, Item XXI (December 1978).
• a color improver, a surface active agent and a hardener may be contained on demand.
• amino compounds such as alkanolamine, described in European Patent Publication 136,582, British Patent 958,678, U.S. Pat. No. 3,232,761, and JP-A-56-106244 can be used for the developing solution of the present invention for the purposes of development acceleration and contrast improvement.
• the fixing solution used in the present invention is an aqueous thiosulfate solution having a pH of 3.8 or more, preferably 4,2 to 7.0.
• a fixing agent includes sodium thiosulfate and ammonium thiosulfate, and ammonium thiosulfate is particularly preferred from a viewpoint of a fixing rate.
• An amount of the fixing agent can suitably be changed and is generally about 0.1 to about 6 mole/liter.
• the fixing solution may contain water soluble aluminum salts which act as a hardener and include, for example, aluminum chloride, aluminum sulfate and potassium alum.
• Tartaric acid, citric acid, gluconic acid or the derivatives thereof may be used for the fixing solution singly or in combination of two or more kinds. These compounds are effectively contained in the fixing solution in an amount of 0.005 mole/liter, particularly effectively 0.01 mole/liter to 0.03 mole/liter.
• the fixing solution may contain a preservative (for example, sulfite and bisulfite), a Ph buffer agent (for example, acetic acid and boric acid), a Ph controller (for example, sulfuric acid and ammonia), a chelating agent having a softening ability, a surface active agent, a humidifier, a fixing accelerator, and the compounds described in JP-A-62-78551, if desired.
• a preservative for example, sulfite and bisulfite
• a Ph buffer agent for example, acetic acid and boric acid
• a Ph controller for example, sulfuric acid and ammonia
• a chelating agent having a softening ability for example, a surface active agent, a humidifier, a fixing accelerator, and the compounds described in JP-A-62-78551, if desired.
• the fixing accelerator includes, for example, the thiourea derivatives described in JP-A-45-35754, JP-A-58-122535, and JP-A-58-122536, alcohol having a triple bond in a molecule, and the thioether compounds described in U.S. Pat. No. 4,126,459. Further, the compounds described in JP-A-2-44355 may be used. The compounds described in JP-A-64-4739 can be used as a dye-eluting accelerator.
• processing is carried out with a washing water or stabilizing solution after the developing and fixing processings, followed by drying.
• the processing can be carried out as well in the washing water or stabilizing solution of a replenishing amount of 3 liter or less (including 0, that is, washing with stored water) per m 2 of a silver halide light-sensitive material. That is, not only a water-saving processing gets possible but also piping for installing an automatic developing machine can be unnecessary.
• a multi-stage countercurrent system (for example, 2 stages and 3 stages) has so far been known as a method for reducing a replenishing amount of washing water.
• Application of this multi-stage countercurrent system allows a light-sensitive material after fixing to be proceeded to a cleaner direction, that is, contacting in succession the processing solutions which are not stained by a fixing solution, and therefore more efficient washing can be carried out.
• washing bath with a squeeze roller and a crossover roller described in JP-A-63-18350 and JP-A-62-287252.
• Addition of various oxidizing agents and filtration with a filter may be combined for reduction of a public pollution load which is a problem in washing with a small amount of water.
• an antimoled treatment is preferably provided to washing water or a stabilizing solution.
• a UV irradiating method described in JP-A-60-263939 a method using a magnetic field described in JP-A-60-263940, a method using an ion exchange resin to make pure water, described in JP-A-61-131632, and a method using a disinfectant, described in JP-A-62-115154, JP-A-62-153952, JP-A-62-220951, and JP-A-62-209532.
• the disinfectants, the fungicides and the surface active agents each described in L. F. West, "Water Quality Criteria” Photo. Sci. & Eng. Vol. 9, No. 6 (1965), M.
• isothiazolidine compounds described in J. Imaging Tech., 10 (6) page 242 written by R. T. Kreiman and the compounds described in Research Disclosure, Vol. 205, No. 20526 (1981, No. 4) can be used as well in combination as a microbiocide.
• an overflow solution from a washing or stabilizing bath which is generated by replenishing water provided with an anti-mold treatment according to the method of the present invention to the washing or stabilizing bath depending on a processing, can be utilized as well for a processing solution having a fixing function the preceding bath thereof, as described in JP-A-60-235133.
• the developing time thereof is 5 seconds to 3 minutes, preferably 8 seconds to 2 minutes.
• the developing temperature thereof is preferably 18° C. to 50° C., more preferably 24° C. to 40° C.
• Temperature and time for fixing process are preferably about 18° C. to about 50° C. and 5 seconds to 3 minutes, more preferably 24° C. to 40° C. and 6 seconds to 2 minutes, respectively. Sufficient fixing can be carried out in these ranges, and a sensitizing dye can be eluted to an extent without forming a residual color.
• a temperature and time for washing (or stabilizing) process are preferably 5° to 50° C. and 6 seconds to 3 minutes, more preferably 15° to 40° C. and 8 seconds to 2 minutes, respectively.
• a light-sensitive material subjected to developing, fixing and washing (or stabilizing) process is dried by washing water with squeezing, that is, passing thereof through squeezing rollers. Drying is carried out at about 40° C. to 100° C., and drying time is suitably changed according to an environmental condition. It is usually about 4 seconds to 3 minutes, particularly preferably about 5 seconds to 1 minute at 40° C. to 80° C.
• a developing solution containing the compound of the present invention represented by formula (II) was prepared in a manner as shown in Table-1.
• a developing solution containing hydroquinone as a principal component also was prepared as a comparative example.
• the developing solution shown in Table-1 was diluted by 100 times to measure COD (chemical oxygen demand) according to 18 of JIS K 0102. The results thereof are shown as well in Table-1.
• the developing solutions of the present invention show as very low COD as 1/10 or less as compared with the developing solutions using the conventional hydroquinone developing agents. This shows that not only this developing solution per se. has less risk from an ecological and toxicological point of view, but also in the case where this developing solution is used to carry out a development process with a conventional automatic developing machine, a load to an environment due to a developing solution component mixed in an overflow of a washing bath, that is, a contamination degree to an environment due to a washing waste is considered as being.
• a aqueous gelatin solution containing 1.5 ⁇ 10 -4 mole/liter of 1,3-dimethyl-2-imidazolidinethione and 7 ⁇ 10 -2 mole/liter of sodium chloride was maintained at 40° C. and was mixed.
• a mixed aqueous solution of sodium chloride and sodium bromide containing potassium hexachloroiridate (III) of 2 ⁇ 10 -7 mole and ammonium hexachlororhodate (III) of 3 ⁇ 10 -7 mole each per mole of silver
• an aqueous silver nitrate solution by a double jet method over a period of 30 minutes, to thereby prepare a silver chlorobromide emulsion (silver bromide content: 30 mole %) having an average grain size of 0.25 ⁇ m and comprising monodispersed cube grains (fluctuation coefficient: 9.5%).
• the emulsion was washed according to a conventional manner to remove soluble salts. Then, gelatin was added and sodium chloride, sodium bromide and sodium hydroxide were further added to adjust Pag and Ph to 7.5 and 6.0, respectively, followed by adding sodium sulfate of 2 ⁇ 10.sup. ⁇ 5 mole and potassium chloraurate of 3 ⁇ 10 -5 mole each per mole of silver to this emulsion to provide a chemical sensitization at 60° C. for 40 minutes.
• the compound (a) of 1 ⁇ 10 -3 mole per mole of silver was added to prepare the emulsion A.
• Emulsion A0 This emulsion was designated as Emulsion A0, and the emulsions to which the hydrazine compounds I-71, I-72 and I-73 of formula (I) were added in an amount of 6 ⁇ 10 -4 mole per mole of silver were designated as Emulsions A1, A2 and A3, respectively.
• a gelatin layer was coated as a protective layer on a silver halide emulsion layer.
• a gelatin amount in the protective layer was adjusted to 1.2 g per m 2 .
• amorphous SiO 2 of 40 mg/m 2 having an average particle size of 3.5 ⁇ m as a matting agent, silicon oil of 20 mg/m 2 , sodium p-dodecylbenzenesulfonate of 60 mg/m 2 as a coating aid, and the fluorine surface active agent represented by (d) of 5 mg/m 2 .
• Exposure was given to the samples described above with tungsten light of 3200° K. for 5 seconds through an optical wedge for a sensitometry, and D-3, D-4, D-5 and D-6 among the developing solutions having the above compositions (Table-1) were used to carry out development at 35° C. for 30 seconds, followed by carrying out fixing, washing and drying processings.
• GR-F1 manufactured by Fuji Photo Film Co., Ltd. was used as a fixing solution.
• the automatic developing machine FG-680A manufactured by Fuji Photo Film Co., Ltd. was used for this development process.
• a sensitivity was shown by a relative value of a reciprocal of an exposure giving a density of 1.5.
• the ( ⁇ ) value shows that the larger the ( ⁇ ) value is, the harder the photographic characteristic. is.
• a black spot was evaluated by five grades by observing an image portion with a loupe.
• Grade (5) shows the best level, at which the black spot is not generated;
• Grade (1) shows the worst level, at which the black spot is markedly generated;
• Grade (3) is a limit level at which the generation of the black spot is practically allowable.
• the high sensitivity and contrast ( ⁇ ) can be obtained with the developing solutions having Ph of 10 or higher and 12 or less. Particularly in the case where a nucleation accelerator was used in combination an image having a higher contrast was obtained at lower Ph. Controlling Ph to 12.5 increased a black spot beyond an allowable level and raised a fogging level as well. On the contrary, a contrast has been reduced.
• Emulsion A4 was prepared in the same manner as in Example 1, except that the emulsion to which the following compound (e) of 5 ⁇ 10 -4 mole per mole of silver was added was used in place of the sensitizing dye (Compound b) contained in the samples of Example 1.
• the samples containing the hydrazine compounds I-69, I-71 and I-73 represented by formula (I) and the nucleation accelerators A-54 and A-73 in this emulsion as shown in Table-4 were prepared in the same manner as in Example 1. ##STR14##
• use of the silver halide light-sensitive material containing the compound of the present invention and the image-forming process using the developing solution containing the compound of the present invention can provide an image free of a black speck and a fog and having a high contrast using a developing solution having a high safety.

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• 1993
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• 1994
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