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
  • 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
  • G03C1/067—Additives for high contrast images, other than 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
  • G03C5/305—Additives other than developers

Definitions

• the invention relates to a method of processing a high contrast silver halide photographic light-sensitive material, and particularly to a method of processing a high contrast silver halide photographic light-sensitive material with less replenishing.
• the photomechanical film-making process comprises a process of converting a half-tone image to a dot image.
• the technique according to an infectious development has been used for reproduction of a high contrast image.
• An image of high contrast and high resolution can be obtained by processing a lith type silver halide photographic light-sensitive material with an alkaline hydroquinone developer having a low concentration of a sulfite ion, so-called, a lith type infectious developer.
• An object of the invention is to provide a method of processing a silver halide photographic light-sensitive material with less replenishment wherein photographic properties thereof are less deteriorated.
• the above object of the invention can be attained by a method of processing a silver halide photographic light-sensitive material comprising a support and provided thereon, a silver halide emulsion layer comprising silver halide grains having not less than 90 mol % chloride, the emulsion layer or a hydrophilic colloid layer adjacent to the emulsion layer containing a tetrazolium compound or a hydrazine derivative, and replenisher for developer being supplied to the developer in an amount of not more than 200 ml per m2 of the material, wherein the developer contains a carbonate salt in an amount of not less than 0.2 mol/litre.
• the developer contains not less than 1.6 ⁇ 10 ⁇ 2 mol/litre of boric acid or a borate or has not less than 0.2 of a ratio of a potassium ion to a sodium ion. It is more preferable that the developer contains not less than 1.6 ⁇ 10 ⁇ 2 mol/litre of boric acid or a borate and has not less than 0.2 of a ratio of a potassium ion to a sodium ion.
• the hydrophilic colloid layer of the invention which is adjacent to the silver halide emulsion layer refers to an intermediate layer, an antihalation layer or a protective layer, each containing no silver halide grains, or another emulsion layer containing silver halide grains.
• the hydrazine derivative is contained in at least one hydrophilic colloid layer on the silver halide emulsion layer side, and may be contained in the different two layers. It is especially preferable that it is contained in the silver halide emulsion layer and/or at least one hydrophilic colloid layer adjacent to the emulsion layer.
• A represents a substituted or unsubstituted aliphatic, aryl or heterocyclic group.
• the aliphatic group represented by A is preferably a group having 1 to 30 carbon atoms, and more preferably a straight-chained, branched or cyclic alkyl group having 1 to 20 carbon atoms.
• the examples thereof include a methyl, ethyl, t-butyl, octyl, cyclohexyl and benzyl group, each of which may have a substituent such as an aryl, alkoxy, aryloxy, alkylthio, arylthio, sulfoxy, sulfonamide, acylamino, or ureido group.
• the aryl group represented by A in Formula [H] is preferably a single or condensed ring group, for example, a benzene ring group or a naphthalene ring group.
• the heterocyclic group represented by A in Formula [H] is preferably a single or condensed ring group containing a hetercycle having one hetero atom selected from a nitrogen, sulfur and oxygen atom, such as a pyrrolidine ring, an imidazole ring, a tetrahydrofuran ring, a morpholine ring, a pyridine ring, a pyrimidine ring, a quinoline ring, a thiazole ring, a benzothiazole ring, a thiophene ring or a furan ring.
• a nitrogen, sulfur and oxygen atom such as a pyrrolidine ring, an imidazole ring, a tetrahydrofuran ring, a morpholine ring, a pyridine ring, a pyrimidine ring, a quinoline ring, a thiazole ring, a benzothiazole ring, a thioph
• the group represented by A preferably represents an aryl group or a heterocyclic group.
• the aryl or heterocyclic group may have a substituent.
• the examples of the substituent include an alkyl group (preferably having 1 to 20 carbon atoms), an aralkyl group (preferably a single or condensed ring group having an alkyl group of 1 to 3 carbon atoms), an alkoxy group (preferably having an alkyl group of 1 to 20 carbon atoms), a substituted amino group (preferably having an alkyl group or alkylidene group of 1 to 20 carbon atoms), an acylamino group (preferably having 1 to 40 carbon atoms), a sulfonamide group (preferably having 1 to 40 carbon atoms), a ureido group (preferably having 1 to 40 carbon atoms), a hydrazinocarbonylamino group (preferably having 1 to 40 carbon atoms), a hydroxy group or a phosphoamide group (preferably having 1 to 40 carbon atoms).
• the group represented by A preferably has at least one of a non-diffusible group and a group for promoting silver halide adsorption.
• the non-diffusible group is preferably a ballast group which is conventionally used in immobile photographic additives such as couplers, and the ballast group includes an alkyl, alkenyl, alkinyl or alkoxy group having not less than 8 carbon atoms or a phenyl, phenoxy or alkylphenoxy group, which is relatively inactive to photographic properties.
• the group for promoting silver halide adsorption includes a thiourea, thiourethane, mercapto, thioether, thion, heterocyclic, thioamidoheterocyclic or mercaptoheterocyclic group or an adsorption group described in column 12, line 19 to column 18, line 7 of Japanese Patent O.P.I. Publication No. 64-90439/1989.
• the example of B includes an acyl group (for example, formyl, acetyl, propionyl, trifluoroacetyl, methoxyacetyl, phenoxyacetyl, methylthioacetyl, chloroacetyl, benzoyl, 2-hydroxymethylbenzoyl, 4-chlorobenzoyl), an alkylsulfonyl group (for example, methanesulfonyl, chloroethanesulfonyl), an arylsulfonyl group (for example, benzenesulfonyl), an alkylsulfinyl group (for example, methanesulfinyl), an arylsulfinyl group (for example, benzenesulfinyl), a carbamoyl group (for example, methylcarbamoyl, phenylcarbamoyl), an alkoxycarbonyl group (for example, methoxycarbon
• B is preferably an acyl group.
• A1 and A2 represent both hydrogen atoms or one of A1 and A2 represents a hydrogen atom and the other represents an acyl group (acetyl, trifluoroacetyl, benzoyl), a sulfonyl group (methanesulfonyl, toluenesulfonyl) or an oxalyl group (ethoxalyl).
• acyl group acetyl, trifluoroacetyl, benzoyl
• a sulfonyl group methanesulfonyl, toluenesulfonyl
• oxalyl group ethoxalyl
• a compound represented by the following Formula [H'] is preferable.
• C represents the same as A in Formula [H]
• D represents or -OR8 wherein R6 and R7 independently represent a hydrogen atom, a substituted or unsubstituted alkyl, alkenyl, alkinyl, aryl, or heterocyclic group, a substituted or unsubstituted alkoxy, alkenyloxy, alkinyloxy, aryloxy or heterocyclicoxy group, an amino group or a hydroxy group, provided that R6 and R7 may form a ring together with a nitrogen atom, R8 represents a hydrogen atom or a substituted or unsubstituted alkyl, alkenyl, alkinyl, aryl or heterocyclic group.
• the compound represented by the following Formula [Ha] is especially preferable: wherein R11 represents a substituted or unsubstituted aryl or heterocyclic group, R12 represents group and -OR15 group wherein R13 and R14 independently represent a hydrogen atom, a substituted or unsubstituted alkyl, alkenyl, alkinyl, aryl or heterocyclic group, a substituted or unsubstituted alkoxy, alkenyloxy, alkinyloxy, aryloxy or heterocyclicoxy group, an amino group or a hydroxy group, provided that R13 and R14 may form a ring together with a nitrogen atom, R15 represents a hydrogen atom or a substituted or unsubstituted alkyl, alkenyl, alkinyl, aryl or heterocyclic group, and A3 and A4 are the same as A1 and A2 of Formula [H], respectively.
• the aryl group represented by R11 is preferably a single or condensed ring group, for example, a benzene ring group or a naphthalene ring group.
• the heterocyclic group represented by R11 is preferably a single or condensed ring group comprising a 5- or 6-membered heterocycle having one hetero atom selected from a nitrogen, sulfur and oxygen atom, such as a pyridine ring, a quinoline ring, a pyrimidine ring, a thiophene ring, a furan ring, a thiazole ring or a benzothiazole ring.
• R11 is preferably a substituted or unsubstituted aryl group.
• the substituent is the same as that of A in Formula [H].
• R11 is preferably a group having at least one sulfo group when a developer having pH of not more than 11.2 is used for high contrast.
• A3 and A4 are the same as A1 and A2 of Formula [H], respectively, and are preferably simultaneously hydrogen atoms.
• R12 represents group and -OR15 group wherein R13 and R14 independently represent a hydrogen atom, a substituted or unsubstituted alkyl group (methyl, ethyl or benzyl), a substituted or unsubstituted alkenyl group (allyl, butenyl), a substituted or unsubstituted alkinyl group (propagyl, butinyl), a substituted or unsubstituted aryl group (phenyl, naphthyl), a substituted or unsubstituted heterocyclic group (2,2,6,6-tetramethylpiperidinyl, N-benzylpiperidinyl, quinolidinyl, N,N'-diethylpyrazolidinyl, N-benzylpyrrolidinyl, pyridyl), a substituted or unsubstituted amino group (amino, methylamino, dimethylamino, dibenzylamino),
• a compound represented by the following Formula [H-a'] is preferable.
• E represents the same as A in Formula [H] and F represents or -OR15 wherein R13 and R14 independently represent a hydrogen atom, a substituted or unsubstituted alkyl, alkenyl, alkinyl, aryl, or heterocyclic group, a substituted or unsubstituted alkoxy, alkenyloxy, alkinyloxy, aryloxy or heterocyclicoxy group, an amino group or a hydroxy group, provided that R13 and R14 may form a ring together with a nitrogen atom, R15 represents a hydrogen atom or a substituted or unsubstituted alkyl, alkenyl, alkinyl, aryl or heterocyclic group.
• the content of the compound of the invention represented by Formula [H] is preferably 5 ⁇ 10 ⁇ 7 to 5 ⁇ 10 ⁇ 1 mol/mol of silver, and more preferably 5 ⁇ 10 ⁇ 6 to 5 ⁇ 10 ⁇ 2 mol/mol of silver.
• the compound represented by Formula [H] is contained in the silver halide emulsion layer or its adjacent hydrophilic colloid layers of a photographic light sensitive material.
• the silver halide photographic light-sensitive material of the invention preferably contains the following nuclear promoting agent to promote nuclear development.
• the nuclear promoting agent includes a compound represented by the following Formula [Na] or [Nb]:
• R1, R2 and R3 independently represent a hydrogen atom, an alkyl group, a substituted alkyl group, an alkenyl group, a substituted alkenyl group, an alkinyl group, a substituted alkinyl group, an aryl group or a substituted aryl group, provided that R1, R2, and R3 are not simultaneously hydrogen atoms and R1, R2 and R3 may form a ring together.
• the preferable agent is an aliphatic tertiary amines. These compounds preferably have in the molecules an anti-diffusible group or a silver halide adsorption group.
• the compounds having anti-diffusible property have preferably a molecular weight not less than 100, and more preferably a molecular weight not less than 300.
• the preferable adsorption group include a heterocyclic, mercapto, thioether, thion or thiourea group.
• Ar represents a substituted or unsubstituted aryl or heterocyclic group
• R represents a hydrogen atom or an alkyl group, an alkenyl group, an alkinyl group or an aryl group , each of which may have a substituent.
• These compounds preferably have in the molecules an anti-diffusible group or a silver halide adsorption group.
• the compounds having anti-diffusible property have preferably a molecular weight not less than 120, and more preferably a molecular weight not less than 300.
• R1, R2, R3 and R4 independently represent a hydrogen atom, an alkyl group, a substituted alkyl group, an alkenyl group, a substituted alkenyl group, an alkinyl group, a substituted alkinyl group, an aryl group, a substituted aryl group or a saturated or unsaturated heterocyclic group, provided that R1, R2, R3 and R4 may form a ring together, R1 and R2 are not simultaneously hydrogen atoms, and R3 and R4 are not simultaneously hydrogen atoms.
• the preferable agent is an aliphatic tertiary amine.
• nuclear promoting agents those having at least one -(CH2CH2O)- group are more preferable.
• the tetrazolium compound used in the light-sensitive material of the invention is generally represented by the following formula (T).
• the substituents R1, R2 and R3 on the phenyl group of the triphenyltetrazolium compound represented by Formula (T) preferably represent a hydrogen atom or a group having a negative or positive Hammett's sigma value ( ⁇ P), which is a measure of the electron withdrawing property. Particularly preferred are those having a negative Hammett's sigma value.
• Hammett's sigma value in phenyl substitution can be seen in various literatures, for example, in C. Hansch's report in Journal of Medical Chemistry, Vol. 20, p. 304 (1977).
• Those having a particularly preferred negative sigma value include, for example, methyl ( ⁇ P: -0.17, a value hereinafter given in parentheses is ⁇ P), ethyl (-0.15), cyclopropyl (-0.21), n-propyl (-0.13), iso-propyl (-0.15), cyclobutyl (-0.15), n-butyl (-0.18), iso-butyl (-0.20), n-pentyl (-0.15), cyclohexyl (-0.22), amino (-0.66), acethylamino (-0.15), hydroxyl (-0.37), methoxy (-0.27), ethoxy (-0.24), propoxy (-0.25), buthoxy (-0.32)
• n 1 or 2
• X ⁇ represents an anion
• the anion represented by X ⁇ includes, for example, halogen ions such as a chloride ion, a bromide ion, or a iodide ion; acid residues of inorganic acids such as nitric acid, sulfuric acid, perchloric acid; acid residues of organic acids such as sulfonic acids, carboxylic acids, and anions of anionic surfactants, for example, lower alkylbenzene sulfonic acid anions such as a p-toluenesulfonic acid anion; higher alkylbenzene sulfonic acid anions such as a p-dodecylbenzene sulfonic acid anion; higher alkyl sulfate anions such as a lauryl sulfate anion; boron type anions such as a tetraphenyl boron; dialkyl sulfosuccinate anions such as a di-2-ethyl
• the tetrazolium compounds represented by formula (T) may be used singly or in combination of two or more kinds at a proper ratio.
• the silver halide emulsion used in the light-sensitive material in the invention may be obtained by any of an acidic, neutral and ammonium method, and comprises grains having a particle size of preferably 0.2 to 0.5 ⁇ m.
• water soluble rhodium or iridium salts are added to the emulsion to contain the salts inside or on the surface of the grains.
• the adding amount of the salts is preferably 10 ⁇ 6 to 10 ⁇ 9 mol of mol of silver.
• the silver halide grains are silver chloride or silver bromochloride or silver iodobromochloride containing not less than 90 mol% of silver chloride.
• the grains may be grains having a uniform halide composition or core/shell grains where the halide composition inside the grains is different from that of the outer layer of the grains.
• the grains may be ones forming a latent image mainly on the surface or ones a latent image forming mainly inside the grains.
• the silver halide grains in any form can be used in the invention.
• One preferable example is cubic grains having ⁇ 100 ⁇ face as a crystal surface.
• the octahedral, tetradecahedral or dodecahedral grains are prepared according to a method described in U.S. Patent Nos. 4,183,756 and 4,225,666, Japanese Patent O.P.I. Publication No. 55-26589, Japanese Patent Publication No. 55-42737 or J. Photgr. Sci., 21, 39(1973) and can be used. Grains having a twin plane may also be used.
• the silver halide grains in the invention may be in a single form or in a mixture of various forms.
• the silver halide emulsion in the invention may have any particle size distribution.
• the silver halide emulsion having a broad particle size distribution (polydisperse emulsion) or a narrow particle size distribution (monodisperse emulsion) may be used singly or in admixture of several kinds of the emulsions.
• the polydisperse emulsion and monodisperse emulsion may be used in combination. Two or more kinds of silver halide emulsions prepared separately may be used in combination.
• the monodisperse emulsion is preferably used in the invention.
• the monodisperse silver halide grains in the monodisperse emulsion are grains comprising grains having a particle size falling within ⁇ 20% of a deviation from an average particle size, r in an amount preferably not less than 60 % by weight, more preferably not less than 70 % by weight, and most preferably not less than 80 % by weight based on the total silver halide grains.
• r is defined to be particle size r i when n i ⁇ r i 3 is maximum, wherein n i represents frequency of grains having a particle size of r i . (The number of significant figures is three from the maximum digit, and the calculated figure is rounded off to the three digit)
• the particle size referred to herein is the diameter when silver halide grains are spherical, and the diameter of a circle to which the area of the projected image of the grains is converted, when in a shape other than a sphere.
• the particle size can be obtained by measuring the grain diameter or an area of the projected image of the grains on a print which were photographed magnified 10,000 to 50,000 times by an electonmicroscope (the number of grains should be not less than 1000 selected randomly).
• the high monodisperse emulsion of the invention has a monodisperse degree of preferably not more than 20, and a monodisperse degree of more preferably not more than 15.
• the average particle size and standard deviation of the particle size can be obtained by r i as defined above.
• the monodisperse emulsion can be obtained by a method described in Japanese Patent O.P.I. Publication Nos. 54-48521, 58-49938 and 60-122935.
• the light sensitive silver halide emulsion used in the invention can be a chemically unsensitized emulsion, which is called a primitive emulsion, but is usually chemical-sensitized.
• a chemical sensitization method is used a method described in the aforementioned literature by Glafkides or Zelikman, or "Die Grundlagen der Photographischen mit Silberhalogeniden” edited by H. Frieser, Akademische Verlagsgesellschaft (1968).
• There is a sulfur sensitization method using a sulfur-containing compound or active gelatin capable of reacting with silver ion a reduction sensitization method using a reducing agent or a method using gold or other noble metals.
• the sulfur sensitizer includes a thiosulfate, a thiourea, a thiazole, a rhodanine, and so forth.
• the example thereof is described in U.S. Patent Nos. 1,574,944, 2,410,689, 2,278,947, 2,728,668 and 3,656,955.
• the reduction sensitizer includes a stannous salt, amines, a hydrazine derivative, formamidinesulfinic acid, and a silane compound.
• the example thereof is described in U.S. Patent Nos. 2,487,850, 2,419,974, 2,518,698, 2,983,609, 2,983,610 and 3,694,637.
• the noble metal sensitizer includes a gold complex or a complex of a metal belonging to the VII Group of the Periodic Table such as platinum, iridium or palladium and examples thereof is described in U.S. Patent Nos. 2,399,083 and 2,448,060 or British Patent No. 618,061.
• the pH, pAg or temperature during the chemical sensitization is not specifically limited, but the pH is 4-9, and preferably 5-8, the pAg is 5-11, and preferably 7-9, and the temperature is 40-90°C, and preferably 45-75°C.
• the photographic emulsion used in the invention is subjected to the above sulfur or gold-sulfur sensitization and further to reducing sensitization using a reducing agent or noble metal sensitization.
• the above emulsion may be used singly or two kinds or more kinds of emulsions in combination.
• various stabilizing agents such as 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene, 5-mercapto-1-phenyltetrazole and 2-mercapto-benzothiazole are used.
• Silver halide solvent like thioethers, mercapto group-containing compounds or crystal habit controlling agents like sensitizing dyes may be optionally used.
• the unnecessary soluble salts in the emulsion in the invention may be removed after completion of silver halide growth, and the emulsion may contain the soluble salts.
• the salts can be removed according to a method described in Research Disclosure 17643.
• the various additives can be added to the above photographic emulsion in the invention in order to prevent lowering of sensitivity and occurrence of fog in the process of its manufacturing or during its storing or processing. That is, to the emulsion can be added, compounds well known as stabilizers, azoles such as benzothiazolium salts, nitroindazoles, triazoles, benzotriazoles or benzimidazoles (especially, ones having a nitro or halogen group), mercapto heterocyclic compounds such as mercaptothiazoles, mercaptobenzimidazoles, mercaptotetrazoles (especially, 1-phenyl-5-mercaptotetrazole) or mercaptopyridines, the above heterocyclic compounds or mercapto compounds having a water solubilizing group such as a carboxyl group or a sulfo group, thioketone compounds such as oxazolinethions, azaindenes such as tetraazainden
• the silver halide photographic light-sensitive material in the invention can contain in its photographic structural layer alkylacrylate latexes described in U.S. Patent Nos. 3,411,911 and 3,411,912 and Japanese Patent Publication No. 45-5331.
• the silver halide photographic light-sensitive material in the invention may contain the following various additives.
• the thickener or plasticizer includes a compound such as styrene-sodium maleate copolymer or dextrane sulfate described in U.S. Patent No. 2,960,404, Japanese Patent Publication No.43-4939, German Patent Publication No. 1,904,604, Japanese Patent O.P.I. Publication No. 48-63715, Belgium Patent No. 762,833, U.S. Patent No. 3,767,410, and Belgium Patent No. 588,143.
• the hardener includes aldehydes, epoxy compounds, ethyleneimines, active halogenides, vinylsulfones, isocyanates, sulfonic acid esters, carbodiimides, mucochloric acid or acyloyls.
• the UV absorbent includes a compound described in U.S. Patent No. 3,253,921 and British Patent No.
• 1,309,349 such as 2-(2'-hydroxy-5-tert-butylphenyl)benzotriazole, 2-(2'-hydroxy-3',5'di-tert-butylphenyl)benzotriazole, 2-(2-hydroxy-3'-tert-butyl-5'-butylphenyl)-5-chlorobenzotriazole or 2-(2'-hydroxy-3',5'-di-tert-butylphenyl)-5-chlorobenzotriazole.
• the surfactants which are used as an agent improving permeability of an auxiliary coating agent, an emulsifier or processing solutions, an anti-forming agent or various agents for controlling physical properties of light sensitive materials, include an anionic, cationic or nonionic surfactant described in British Patent Nos. 548,532 and 1,216,389, U.S. Patent No. 2,026,202 and 3,514,293, Japanese Patent Publication Nos. 44-26580, 43-17922, 43-17926, 43-3166 and 48-20785, French Patent No. 202,588, Belgium Patent No. 773,459 and Japanese Patent O.P.I. Publication No. 48-101118.
• the anti-static agent includes compounds described in Japanese Patent Publication No. 46-24159, Japanese Patent O.P.I. Publication No. 48-89979, U.S.Patent Nos. 2,882,157 and 2,972,535, Japanese Patent O.P.I. Publication Nos.48-20785, 48-43130 and 48-90391, Japanese Patent Publication Nos. 46-24159, 46-39312 and 48-43809 and Japanese Patent O.P.I. Publication No. 47-33627.
• pH of the coating solution is preferably 5.3-7.5.
• the pH of a mixture coating solution, in which a coating solution for each respective coating layer is mixed in respective amounts is preferably 5.3-7.5.
• the pH is lower than 5.3, the hardening speed is low, and when pH is higher than 7.5, photographic properties are adversely affected.
• the light-sensitive material in the invention may contain in its structural layer a lubricant, such as a higher aliphatic alcohol ester described in U.S. Patent Nos. 2,588,756 and 3,121,060, casein described in U.S. Patent No. 3,295,979, a higher aliphatic calcium salt described in British Patent No. 1,623,722 or a silicone compound described in British Patent No. 1,313,384, U.S. Patent Nos. 3,042,522 and 3,489,567.
• a liquid paraffin dispersion can also be used for this purpose.
• Additive RD17643 RD18716 1. Chemical sensitizer p.23 p.648, r.col. 2. Sensitivity increaser -ditto- 3. Spectral sensitizer pp.23 ⁇ 24 p.648, r.col. Supersensitizer p.649, r.col. 4. Whitening agent p.24 5.
• Antifoggant & stabilizer pp.24 ⁇ 25 p.649, r.col. 6.
• Light absorbent & filter dye pp.25 ⁇ 26 p.649, r.col.
• UV absorbent p.650, l.col. 7.
• Dye-image stabilizer p.25 9.
• Coating aid & surfactant pp.26 ⁇ 27 -ditto- 13.
• the processing method of the silver halide photographic light-sensitive material in the invention is not specifically limited, and various processing methods can be used.
• the processing temperature is usually 18 to 50°C, but temperatures lower than 18°C or higher than 50°C can be employed.
• the following developing agent of a black and white developer is used singly or in combination: dihydroxy benzenes like hydroquinone, 3-pyrazolidone like 1-phenyl-3-pyrazolidone, and aminophenols like N-methyl-p-aminophenol.
• the developer used in the invention further contains an alkali agent.
• the developer of the invention contains a carbonate salt in an amount of preferably 0.2 to 1.0 mol/liter, and more preferably 0.35 to 0.7 mol/liter.
• the developer of the invention further contains boric acid or a borate in an amount of preferably 1.6 ⁇ 10 ⁇ 2 to 3.3 ⁇ 10 ⁇ 1 mol/liter, more preferably 4.85 ⁇ 10 ⁇ 2 to 1.6 ⁇ 10 ⁇ 1 mol/liter, and still more preferably 8.0 ⁇ 10 ⁇ 2 to 1.3 ⁇ 10 ⁇ 1 mol/liter.
• the ratio, potassium ion/sodium ion in the developer of the invention is preferably 0.2 to 10, and more preferably 0.5 to 2.
• the replenisher for developer is supplied to the developer in an amount of preferably 50 to 200 ml per m2 of the material.
• the silver halide photographic light-sensitive material in the invention can be processed with a developer containing imidazols as a silver halide solvent or a developer containing the silver halide solvent and additives such as indazoles or triazols.
• the developer usually contains various preservatives, alkali agents, pH buffering agents, or anti-foggants, and further optionally contains an auxiliary solubility agent, a development accelerator, a surfactant, an anti-foaming agent, a water softening agent, a hardener or a viscosity increasing agent.
• a fixer having a conventional composition can be used.
• the fixer may contain a soluble aluminum salt as a hardener.
• the exposure of the photographic emulsion in the invention can be carried out using various light sources such as tungsten lamps, fluorescent lamps, an arc lamp, a mercury lamp, a xenon-sunlight lamp, a xenon flash, a cathode-ray tube flying spot, a laser light, an electron beam, a X-ray and a fluorescent screen on a X-ray photographing according to chemical sensitization of the emulsion or objects used.
• the exposure time is usually 1/1000 to 100 seconds, and short exposure time of 10 ⁇ 4 to 10 ⁇ 9 seconds applies in the case of a laser light.
• a silver bromoiodochloride emulsion having a silver chloride content of 90 mol% and a silver iodide content of 0.2 mol% was prepared in a double-jet precipitation method.
• K3RhBr6 was added in an amount of 5.0 ⁇ 10 ⁇ 5 mol/mol of silver.
• the resulting emulsion was proved to be an emulsion comprising cubic monodisperse grains having an average particle diameter of 0.20 ⁇ m (with a variation coefficient of 9%).
• the emulsion was desalted with denatured gelatin disclosed in Japanese Patent O.P.I. Publication No.
• 2-280139 (one in which an amino group in gelatin is substituted with a phenylcarbamyl group, for example, Exemplified compound G-8 in Japanese Patent O.P.I. Publication No. 2-280139).
• the resulting EAg after the desalting was 190mv at 50°C.
• the resulting emulsion was adjusted to be pH 5.58 and EAg 123mv, and the temperature thereof was elevated to 60°C.
• To the emulsion was added 2.2 ⁇ 10 ⁇ 5 mol/mol of silver of chloroauric acid and the mixture was stirred for 2 minutes.
• To the mixture emulsion was added 2.9 ⁇ 10 ⁇ 6 mol/mol of silver of S8 and the mixture was chemically ripened for 78 minutes.
• a 100 ⁇ m thick polyethylene terephthalate film subjected to anti-static treatment disclosed in Example 1 of Japanese Patent O.P.I. Publication No. 3-92175 was coated on the subbing layer on one side with the silver halide emulsion of the following prescription 1 to give a silver content of 3.3g/m2 and a gelatin content of 2.6g/m2.
• As a protective layer the coating solution of the following prescription 2 was coated on the emulsion layer to give a gelatin content of 1g/m2.
• the backing layer of the following prescription 3 was coated on the subbing layer on the other side to give a gelatin content of 2.7g/m2 and the backing protective layer of the following prescription 4 was coated on the backing layer to give a gelatin content of 1g/m2.
• the above obtained sample was in close contact with a step wedge and exposed using a light having a wavelength of 633nm as a representative of He-Ne laser light.
• the exposed material was processed with the following developer and fixer under the following conditions, using a rapid automatic developing machine (GR-26 SR produced by Konica Corporation).
• the sample processed with the processing solutions after 500 sheets of film measuring 508mm ⁇ 610mm was processed in a replenishing amount of 150ml/m2 of developer replenisher and in a replenishing amount of 200ml/m2 of fixer replenisher was evaluated for running processing.
• (Developer Prescription) Sodium sulfite 55g/litre Sodium carbonate shown in Table 1 Hydroquinone 20g/litre 4-methyl-4-hydroxymethyl-1-phenyl-3-pyrazolidone (Dimeson) 0.9g/litre Potassium bromide 5g/litre Benzotriazole 0.16g/litre Boric acid shown in Table 1 Diethyleneglycol 40g/litre 2-mercaptohypoxanthine 60g/litre
• the processed sample was measured using PDA-65 (Konica digital densitometer).
• the sensitivity in Table was indicated by a relative sensitivity to sensitivity at density 3.0 of Sample No.1 regarded as 100.
• the gamma value was measured for evaluation of image sharpness and indicated by a tangent between the densities 0.1 and 3.0. When the gamma value is less than 6, it can not be put into practical use. When the gamma value is 6 to less than 10, it is not a satisfactory contrast.
• the material having a gamma value of not less than 10 gives a ultra high contrast and can be put into practical use. The results are shown in Table 1. Table 1 Sample No.
• the invention shows the less difference in the sensitivity and gamma value between the fresh and processed solutions.
• Monodisperse silver bromochloride grains containing 10 ⁇ 5 mol/mol of silver of a rhodium salt, and having a silver bromide content of 2 mol%, an average particle diameter of 0.20 ⁇ m and a monodisperse degree of 20 were prepared under an acidic atmosphere in a double-jet precipitation method.
• the growth of the grains was carried out in a system containing an aqueous 1 % gelatin solution containing 30mg/litre of benzyladenine. After mixing silver and halides, 600mg of mol of silver of 6-methyl-4-hydroxy-1,3,3a,7-tetrazaindene of 7.5 ⁇ 10 ⁇ 3mol was added to the mixture, and was washed and desalted.
• the coating solution was coated after adjusting to pH 6.5 with sodium hydroxide.
• the following emulsion protective layer was coated to have the following content simultaneously together with the emulsion.
• the coating solution was coated after adjusting to pH 5.4 with citric acid.
• the backing layer was provided on the support side opposite the emulsion layer in the same manner as in Example 2 of Japanese Patent O.P.I. Publication No.2-226134.
• Sample No. 1 obtained above was evaluated in the same manner as in Example 1, except that the following processing condition was carried out. (Processing condition) Processing step Temperature, °C Time, seconds Developing 35 15 Fixing 35 10 Washing room temp. 10 Drying 45 7.5
• Samples were prepared in the same manner as in Example 1, except that the emulsion comprising silver halide grains having a silver chloride content as shown in Table 3 was used.
• the samples above obtained above were processed in the same manner as in Example 1, except that the developer shown in Table 3 was used and evaluated in the same manner as in Example 1. Further, black spots at unexposed portions of the developed samples was counted in terms of the number per 1 x 10 ⁇ 2cm2, using 10 power magnifier.
• Samples were prepared in the same manner as in Example 2, except that the emulsion comprising silver halide grains having a silver chloride content as shown in Table 4 was used.
• the samples above obtained above were processed in the same manner as in Example 1, except that the developer shown in Table 4 was used and evaluated in the same manner as in Example 2. Further, fog of the samples was measured.

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• General Physics & Mathematics (AREA)
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• 1994
  • 1994-09-27 US US08/313,358 patent/USH1608H/en not_active Abandoned
  • 1994-10-03 DE DE69416766T patent/DE69416766T2/de not_active Expired - Fee Related
  • 1994-10-03 EP EP94307236A patent/EP0647880B1/de not_active Expired - Lifetime

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