EP0211437A2 - Verfahren zur Behandlung farbphotographischer Silberhalogenidmaterialien - Google Patents

Verfahren zur Behandlung farbphotographischer Silberhalogenidmaterialien Download PDF

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Publication number
EP0211437A2
EP0211437A2 EP86110788A EP86110788A EP0211437A2 EP 0211437 A2 EP0211437 A2 EP 0211437A2 EP 86110788 A EP86110788 A EP 86110788A EP 86110788 A EP86110788 A EP 86110788A EP 0211437 A2 EP0211437 A2 EP 0211437A2
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EP
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Prior art keywords
silver halide
processing
photographic material
color photographic
silver
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Application number
EP86110788A
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English (en)
French (fr)
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EP0211437B1 (de
EP0211437A3 (en
Inventor
Takatoshi Ishikawa
Tadashi Ogawa
Junya Nakajima
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Fujifilm Holdings Corp
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Fuji Photo Film Co Ltd
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Publication of EP0211437A3 publication Critical patent/EP0211437A3/en
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    • 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
    • G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/407—Development processes or agents therefor
    • G03C7/413—Developers

Definitions

  • This invention relates to a process for processing silver halide color photographic materials, and more particularly to a photographic processing process giving excellent coloring property using an improved color developer.
  • benzyl alcohol when benzyl alcohol is carried in a bleach bath or a blix bath, which is a bath after a color development bath, it causes the formation of a leuco dye of a cyan coupler, which results in reducing the coloring density of cyan dye. Moreover, when benzyl alcohol is carried in water bath which is a post path to a fix bath or the bleach bath, the life of the color images formed is reduced. Accordingly, by the reasons described above, it is preferred that the concentration of benzyl alcohol in a color developer be low.
  • An object of this invention is to provide a processing process for color photographic materials using a color developer containing no or very little benzyl alcohol.
  • a further object of this invention is to provide a processing process for color photographic materials giving very less pollution problems.
  • a silver halide color photographic material comprising a support having thereon at least one.silver halide emulsion layer containing a silver bromide or silver chlorobromide emulsion in which tabular silver halide grains having main crystal planes parallel to each other and an average aspect ratio of at least 5 account for at least 50 percent of the total projected area of the silver halide grains with a color developer containing 8 ml/liter or less of benzyl alcohol.
  • the color developer for use in this invention contains from 8 ml/liter or less and preferably 5 ml/liter or less of benzyl alcohol, including the case in which no benzyl alcohol is present.
  • the color developer for use in this invention preferably contains a known aromatic primary amine color developing agent.
  • Preferred aromatic primary amine color developing agents are p-phenylenediamine derivatives, and specific examples are shown below, although the invention is not restricted to those specifically listed.
  • the p-phenylenediamine derivatives may be in the forms of salts such as the sulfates, hydrochlorides, sulfites, p-toluenesulfonates, etc.
  • the amount of the aromatic primary amine developing agent for the color developer is generally from about 0.1 g to about 20 g, and preferably from about 0.5 g to about 10 g per liter of the developer.
  • the above-described color developing agent may exist in a silver halide color photographic material for simplifying and quickening the processing.
  • the various precursor for the color developing agent For using the color developing agent in the color photographic material, it is preferred to use the various precursor for the color developing agent.
  • such precursors are the indoaniline series compounds described in U.S. Patent 3,342,597, etc.; the Sciff base-type compounds described in U.S. Patent 3,342,599, Research Disclosure, RD No. 14850 (Aug., 1976) ibid., RD No. 15159 (Nov., 1976), etc., the aldol compounds described in ibid., RD No. 13924 (Nov., 1975), the metal complexes described in U.S. Patent 3,719,492, the urethane series compounds described in Japanese Patent Application (OPI) No.
  • the silver halide color photographic material for use in this invention may, if desired, contain various l-phenyl-3-pyrazolidones for accelerating a color development. Examples of these compounds are described in Japanese Patent Application (OPI) No. 64339/81, 144547/82, 211147/82, 50532/83, 50536/83, 50533/83, 50534/83, 50535/83, and 115438/83, etc.
  • the color developer for use in this invention may further contain a hydroxylamine of types known in the art.
  • Such a hydroxylamine may be used in the form of a free amine in the color developer but is generally used in the form of a water-soluble acid salt thereof.
  • these salts are sulfates, oxalates, chlorides, phosphates, carbonates, acetates, etc.
  • the hydroxylamines may be substituted or unsubstituted, and also the nitrogen atom of the hydroxylamines may be substituted by an alkyl group. In particular, the hydroxylamines substituted by a substituted or unsubstituted alkyl group are preferred.
  • the pH of the color developer for use in this invention is preferably from 9 to 12, and more preferably from 9 to 11.0.
  • the color developers for use in this invention may further contain other components known as developer components.
  • Examples include sodium hydroxide, potassium hydroxide, , sodium carbonate, potassium carbonate, sodium tertiary phosphate, potassium tertiary phosphate, potassium netaborate, borax, etc., as an alkali agent or a pH buffer. They can be used solely or as a combination thereof. Also, for giving buffer function to the color developer, facilitating the preparation of the color developer, or increasing the ionic strength of the color developer, various salts such as disodium hydrogenphosphate, dipotassium hydrogenphosphate, potassium dihydrogenphosphate, sodium dihydrogenphosphate, sodium hydrogencarbonate, potassium hydrogencarbonate, borates, an alkali nitrate, an alkali sulfate, etc.
  • various chelating agents may be used for the color developers as a precipitation preventing agent for calcium and magnesium.
  • examples of such agents are polyphosphates, aminopolycarbonates, phosphonocarbonates, aminopolyphosphonates, 1-hydroxyal- kylidene-1,1-diphosphonates, etc.
  • the color developer may, if desired, contain a development accelerator.
  • the development accelerator include various pyrimidium compounds and other cationic compounds, a cationic dye such as phenosafranine, and neutral salts such as thallium nitrate, potassium nitrate described in U.S. Patent 2,648,604, Japanese Patent Publication No. 9503/69, U.S. Patent 3,171,247 etc., polyethylene glycol and derivatives thereof, and nonionic compounds such as polythioethers described in Japanese Patent Publication No. 9304/69, U.S. Patents 2,533,990, 2,531,832, 2,950,970, 2,577,127, etc., and the thioether series compounds described in U.S. Patent 3,201,242, etc.
  • the color developer may further contain sodium sulfite, potassium sulfite, potassium bisulfite, or sodium bisulfite, which is usually used as a preservative.
  • the color developer for use in this invention may further contain, if desired, an antifoggant.
  • an antifoggant examples include alkali metal halides such as potassium bromide, sodium bromide, potassium iodide, etc., and organic antifoggants.
  • organic antifoggants examples include nitrogen-containing heterocyclic compounds such as benzotriazole, 6-nitrobenzimidazole, 5-nitroisoindazole , 5-methylbenzotriazole, 5-nitrobenzotriazole, 5-chloro-benzotriazole, 2-thiazolylbenzimidazole, 2-thiazolylmethylbenzimidazole, hydroxyaza- indrizine, etc., mercapto-substituted heterocyclic compounds such as I-phenyl-5-mercaptotetrazole, 2-mercaptobenzimidazole, 2-mercaptobenzothiazole, etc., and further mercapto-substituted aroamtic compounds such as thiosalicylic acid, etc.
  • the nitrogen-containing heterocyclic compounds are particularly preferred.
  • Such an antifoggant may be used in such a manner that it is dissolved out from a color photographic light-sensitive material and accumulates in a color developer.
  • the silver halide color photographic material is usually bleached after color development.
  • the bleach process may be performed simultaneously with a fix process (blix process) or may be performed separately from a fix process.
  • a bleaching agent there are, for example, compounds of polyvalent metals such as iron(III), cobalt (III), chromium(VI), copper(II), etc., peracids, quinones, nitroso compounds, etc.
  • bleaching agent examples include ferricyanides, dichromates, organic complex salts of iron(III) or cobalt(III), complex salts of aminopolycarboxylic acids such as ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, nitrilotriacetic acid, l,3-diamino-2-propanoltetraacetic acid, etc., or organic acids such as citric acid, tartaric acid, malic acid, etc., persulfates, manganates, nitrosophenol, etc.
  • aminopolycarboxylic acids such as ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, nitrilotriacetic acid, l,3-diamino-2-propanoltetraacetic acid, etc.
  • organic acids such as citric acid, tartaric acid, malic acid, etc., persulfates, manganates, nitrosophenol, etc
  • potassium ferricyanide ethylenediaminetetraacetic acid iron(III) sodium, ethylenediaminetetraacetic acid iron(III) ammonium, triethyl- enetetraaminepentaacetic acid iron(III) ammonium, persulfates, cyclohexanediaminetetraacetic acid iron(III) salt, etc.
  • Ethylenediaminetetraacetic acid iron(III) complex salts are useful in bleach solutions and in blix solutions.
  • the bleach solution or the blix solution may further, if desired, contain various kinds of accelerators.
  • the bleach accelerator include thiourea series compounds as described in U.S. Patent 3,706,561, Japanese Patent Publication Nos. 8506/70 and 26586/74, Japanese Patent Application (OPI) Nos. 32735/78, 36233/78, and 37016/78, thiol series compounds as described in Japanese Patent Application (OPI) Nos. 124424/78, 95631/78, 57831/78, 32736/78, 65732/78, and 52534/79, and U.S. Patent 3,893,858, heterocyclic compounds as described in Japanese Patent Application (OPI) Nos.
  • thiosulfates As a fixing agent for use in this invention, there are thiosulfates, thiocyanates, thioether series compounds, thioureas, a large amount of iodides, etc. In these compounds, thiosulfates are most generally used.
  • sulfites, bisulfites, or carbonyl- bisulfite addition products are preferably used.
  • a washing process is usually performed.
  • various knoum compounds may be used for the purposes of precipitation prevention and of'water saving.
  • a water softener such as an organic phosphoric acid, an aminopolycarboxylic acid, an inorganic phosphoric acid, etc.
  • a sterilizer or an antimold agent for preventing the generation of various bacteria,algae, and molds, a hardening agent such as a magnesium salt or an aluminum salt, or a surface active agent for preventing drying load (increase of energy) or uneven drying of the surface can be used for the washing process.
  • multi-stage countercurrent stabilization as described, e.g., in Japanese Patent Application (OPI) No. 8543/82 may be applied. In this case, 2 to 9 countercurrent baths are required.
  • various kinds of compounds can be used for the stabilization baths for stabilizing the images formed. Examples of these compounds are buffers (e.g., borates, metaborates, borax, phosphates, carbonates, potassium hydroxide, sodium hydroxide, aqueous ammonia, monocarboxylates, dicarboxylates, polycarboxylates, etc.) and formalin for adjusting the pH of the layers.
  • buffers e.g., borates, metaborates, borax, phosphates, carbonates, potassium hydroxide, sodium hydroxide, aqueous ammonia, monocarboxylates, dicarboxylates, polycarboxylates, etc.
  • formalin for adjusting the pH of the layers.
  • water softeners e.g., inorganic phosphoric acids, aminopolycarboxylic acids, organic phosphoric acids, aminopolyphosphonic acids, phosphonocarboxylic acids, etc.
  • sterilizers e.g., prcxel, isothiazolone, 4-thiazolylbenzimidazole, halogenated chenol- benzotriazoles, etc.
  • surface active agents e.g., fluorescent whiening agents, hardening agents, etc.
  • ammonium salts such as ammonium chloride, ammonium nitrate, ammonium sulfate, ammonium phosphate, ammonium sulfite, ammonium thiosulfate, etc. can be also added to the stabilizing bath(s).
  • the tabular silver bromide or silver chlorobromide grains for use in this invention are more excellent in coloring property as the average aspect ratio thereof becomes higher, but the tabular grain silver bromide or silver chlorobromide emulsion wherein the tabular silver halide grains having an average aspect ratio (defined below) of at least 5 (i.e., 5/1), and preferably at least 8, account for at least 50% of the total projected area of the silver halide grains can be advantageously used in this invention with the effect of this invention as compared with ordinary silver bromide or silver chlorobromide emulsions which are used for conventional color photographic light-sensitive materials, and in particular for conventional color photographic papers.
  • the silver halide for use in this invention is preferably silver bromide or silver chlorobromide containing 3 mol% or less of silver iodide.
  • the silver chloride content in the silver chlorobromide is preferably within the range of 15 mole % to 99 mole %.
  • the amount of the silver chloride is more increased.
  • the silver halide grains may differ in halogen composition between the inside and the surface layer thereof or may differ in halogen composition between the central portion and the annular peripheral portion thereof. Also, a mixture of silver halide grains having a uniform halogen composition and silver halide grains having a double layer or multilayer structure may be used.
  • the aspect ratio in this invention is defined as the ratio of the diameter of a circle having the same area as the projected area formed by projecting the parallel main crystal planes of the tabular grains onto a plane which is parallel to the crystal planes, to the thickness of the parallel main crystal plates of the grain.
  • the average diameter of the tabular silver halide grains having the average aspect ratio of at least 5 for use in this invention is preferably from 0.25 ⁇ m to 2.8 ⁇ m, and particularly preferably from 0.45 ⁇ m to 1.9 ⁇ m.
  • the thickness of the tabular grains is generally at most 0.56 ⁇ m, preferably at most 0.38 ⁇ m, more preferably at most 0.2 ⁇ m.
  • the tabular silver halide grains having an average aspect ratio of at least 5 account for at least 50%, preferably at least 70%, and particularly preferably at least 90% of the total projected area of the silver halide grains.
  • the tabular grain silver halide emulsion in this invention can be used in a narrowed distribution about the diameter or the thickness of the tabular silver halide grains. In this invention, it is particularly preferred that the tabular silver halide grains have a distribution of thin thickness.
  • the tabular silver halide grain emulsion for use in this invention is usually prepared by mixing an aqueous solution of a water-soluble silver salt (e.g., silver nitrate) and an aqueous solution of water-soluble halide(s) (e.g., potassium bromide or sodium chloride alone, or a mixture thereof in the presence of an aqueous solution of a water-soluble polymer such as gelatin.
  • a water-soluble silver salt e.g., silver nitrate
  • water-soluble halide(s) e.g., potassium bromide or sodium chloride alone, or a mixture thereof in the presence of an aqueous solution of a water-soluble polymer such as gelatin.
  • the silver halide grains for use in this invention may be formed or physically ripened in the presence of a cadmium salt, a zinc salt, a lead salt, a thallium salt, an iridium salt or a complex salt thereof, a rhodium salt or a complex salt thereof, an iron salt or a complex salt thereof, etc.
  • the silver halide emulsions for use in this invention are usually, after the formation of the silver halide grains, subjected to physical ripening, desalting, and chemical ripening before coating.
  • the silver halide emulsions for use in this invention can be chemically sensitized by a sulfur sensitization method using active gelatin or a sulfur-containing compound capable of reacting silver (e.g., thiosulfates, thioureas, mercapto compounds, rhodanine, etc.); a reduction sensitization method using a reducing material (e.g., stannous salts, amines, hydrazine derivatives, formamidinesulfinic acid, silane compounds, etc.); a noble metal sensitizing method using a metal compound (e.g., a gold complex salt and complex salts of metals belonging to group VIII of the periodic table, such as platinum, iridium, palladium, rhodium, iron etc.), etc. These methods may be used individually or as a combination thereof.
  • a sulfur sensitization method using active gelatin or a sulfur-containing compound capable of reacting silver e.g., thiosulfates, thi
  • the silver halide photographic emulsions for use in this invention are usually spectrally sensitized by photographic sensitizing dyes.
  • dyes which are used for the spectral sensitization are cyanine dyes, merocyanine dyes, complex cyanine dyes, complex mer0 2 cyanine dyes, holopolar cyanine dyes, hemicyanine dyes, styryl dyes, and hemioxonol dyes.
  • sensitizing dyes may be used singly or as a combination thereof.
  • a combination of sensitizing dyes is frequently used for the purpose of supersensitization.
  • the silver halide emulsion for use in this invention may contain a dye having no spectral sensitizing action by itself or a material which does not substantially absorb visible light, but which shows supersensitization when used together with the sensitizing dye(s).
  • Examples of such compound as above, which can be incorporated in the photographic emulsion together with the sensitizing dye(s) are an aminostilbene compound substituted by a nitrogen-containing heterocyclic ring group (e.g., those described in U.S. Patents 2,933,390, 3,635,721, etc.), an aromatic organic acid-formaldehyde condensation product (e.g., those described in U.S. Patent 3,743,510, etc.), a cadmium salt, an azaindene compound, etc.
  • the spectral sensitization can be performed in any stage of the preparation of the silver halide emulsion, said stage being known to be a useful stage. It is most usual to perform the spectral sensitization after completion of chemical sensitization. However,'the spectral sensitization may be performed simultaneously with chemical sensitization, may be performed before performing chemical sensitization, or may be performed before the end of the precipitation formation of silver halide grains as described in U.S. Patents 3,628,960 and 4,225,666.
  • a spectral sensitizing dye is introduced into a silver halide emulsion in split two portions, i.e., a part of the spectral sensitizing dye is introduced into a silver halide emulsion before chemical sensitization and the remaining portion is introduced thereto after the chemical sensitization as described in U.S. Patent 4,225,666.
  • a spectral sensitizing dye may be added to a silver halide emulsion after forming the 80% precipitation of the silver halide different from the method shown in the above-described U.S. Patent.
  • a spectral sensitizing dye can be incorporated in a silver halide emulsion after the completion of the formation of the precipitation of the silver halide and before the chemical sensitization of the emulsion.
  • two or more kinds of mono-dispersed silver halide emulsions each composed of silver halide grains of a different size can be used for silver haiide emulsion layers having substantially same color sensitive property as a mixture thereof in the same emulsion layer or as separate emulsion layers.
  • two or more kinds of poly-dispersed silver halide emulsions or a mixture of a mono-dispersed silver halide emulsion and a poly-dispersed silver halide emulsion may be used as a mixture thereof Or for separate emulsion layers.
  • color coupler in this invention means a compound capable of forming a dye by causing coupling reaction with the oxidation product of an aromatic primary amine developing agent.
  • useful color couplers include naphtholic and phenolic compounds, pyrazolone and pyrazoloazole series compounds, and open chain and heterocyclic ketomethylene compounds.
  • Specific examples of these cyan, magenta, and yellow couplers which can be used for the silver halide photographic materials are described in the patents cited in Research Disclosure, R D No. 17643 (December, 1978), VII-D, and ibid., RD No. 18717 (November, 1979).
  • the color couplers contained in the silver halide photographic materials which are processed by the process of this invention are rendered non-diffusible by having a ballast group or by being polymerized.
  • a two-equivalent coupler having the coupling active position of which is substituted by a coupling releasable group is more preferred than a four-equivalent coupler having a hydrogen atom at the coupling active position thereof since the coating amount of silver can be reduced in the case of using the two-equivalent coupler.
  • couplers capable of providing coloring dyes having a proper diffusibility, non-coloring couplers, DIR couplers, i.e., couplers releasing a development inhibitor with a coupling reaction, or couplers releasing a development accelerator with coupling reaction can be also used in this invention.
  • Typical examples of the yellow couplers for use in this invention include oil protect type acylamide series couplers. Specific examples of these couplers are described in U.S. Patents 2,407,210, 2,875,057, and 3,265,506.
  • two-equivalent yellow couplers are preferably used. Examples of the two-equivalent yellow couplers are the oxygen atom releasing type yellow couplers described in U.S. Patents 3,408,194, 3,447,928, 3,933,501, 4,022,620, etc., and the nitrogen atom releasing type yellow couplers described in Japanese Patent Publication No. 10739/83, U.S. Patents 4,401,752 and 4,326,024, Research Disclosure, RD No.
  • a-pivaloyl- acetanilide series couplers are excellent in fastness, in particular, light fastness of the colored dyes formed therefrom.
  • a-Benzoylacetanilide series couplers are excellent in coloring density.
  • Magenta couplers for use in this invention include oil protect type indazolone series couplers, cyanoacetyl series couplers, preferably 5-pyrazolone series couplers, and pyrazoloazole series couplers such as pyrazolotriazoles.
  • the 3-position of the coupler is substituted by an arylamino group or an acylamino group from the viewpoint of the hue and the coloring density of the colored dyes formed therefrom.
  • Specific examples of such 5-pyrazolone series couplers are described in U.S.
  • the nitrogen atom-releasing groups described in U.S. Patent 4,310,619 and the arylthio groups described in U.S. Patent 4,351,897 are particularly preferred.
  • the 5-pyrazolone series couplers having a ballast group described in European Patent 73,636 give high coloring density.
  • pyrazoloazole series magenta couplers examples include pyrazolobenzimidazoles described in U.S. Patent 3;061,432, preferably the pyrazolo[5,1-c][1,2,4]-triazoles described in U.S. Patent 3,725,067, the pyrazolotetrazoles described in Research Disclosure, RD No. 24220 (June, 1984) and Japanese Patent Application (OPI) No. 33552/85 and the pyrazolopyrazoles described in Research Disclosure, RD No. 24230 (June, 1984), and Japanese Patent Application (OPI) No. 43659/85.
  • Patent 4,500,630 are preferred from the view point of having less yellow side adsorption of the colored dyes formed therefrom,and light fastness.
  • the pyrazolo[1,5-6][1,2,4]triazoles described in European Patent No. 119,860A are more preferred.
  • Cyan couplers for use in this invention include oil protect type naphtholic and phenolic couplers and typical examples of these cyan couplers are the naphtholic couplers described in U.S. Patent 2,474,293 and preferably the oxygen atom releasing type two-equivalent naphthalic couplers described in U.S. Patents 4,052,212, 4,146,396, 4,228,233, and 4,296,200. Also, specific examples of the phenolic cyan couplers are described in U.S. Patents 2,369,929, 2,801,171, 2,772,162, 2,895,826, etc.
  • the cyan couplers having high fastness to humidity and temperature are preferably used in this invention and specific examples of these cyan couplers are the phenolic cyan couplers having an alkyl group having 2 or more carbon atoms at the meta-position of the phenol nucleus as described in U.S. Patent 3,772,002, the Z,5-diacylamino-substituted phenolic couplers described in U.S. Patents 2,772,162, 3,758,308, 4,126,396, 4,334,011, and 4,327,173, West German Patent Application (OLS) No.
  • the silver halide photographic materials for use in this invention may contain a compound releasing a development inhibitor with the progress of development in place of the DIR coupler.
  • Two or more kinds of the above-described couplers may be used in one silver halide emulsion layer, or the same coupler may be used for two or more different silver halide emulsion layers for satisfying the characteristics required for the silver halide photographic material.
  • Each of the couplers described above is incorporated in a silver halide emulsion layer in an amount of generally from 2 x 10 -3 mole to 5 x 10 -1 mole, and preferably from 1 x 10 -2 mole to 5 x 10 -1 mole, per mole of silver in the emulsion layer.
  • the silver halide photographic materials which are processed by the process of this invention may further contain hydroquinone derivatives, aminophenol derivatives, amines, gallic acid derivatives, cathechol derivatives, ascorbic acid derivatives, non-coloring couplers, sulfon- aminophenol derivatives, etc., as a color fog preventing agent or a color mixing preventing agent.
  • the photographic light-sensitive materials for use in this invention may further contain various fading preventing agents.
  • organic fading-preventing agents include hindered phenols such as hydroquinones, 6-hydroxychromans, 5-hydroxycoumarans, spirochromans, p-alkoxyphenols, bisphenols, etc., gallic acid derivatives, methylenedioxybenzenes, aminophenols, hindered amines, and the ether or ester derivatives formed by silylating or alkylating the phenolic hydroxyl groups of these compounds.
  • metal complexes such as (bis-salicycl- aldoxymato)nickel complex and (bis-N,N-dialkyldithio- carbamato)nickel complex can also be used as the fading-preventing agent.
  • the photographic light-sensitive materials for use in this invention can contain an ultraviolet absorbent in the hydrophilic colloid layers thereof.
  • the photographic light-sensitive materials for use in this invention may further contain in the hydrophilic colloid layers thereof water-soluble dyes as filter dyes or for irradiation prevention or halation prevention.
  • the photographic light-sensitive materials for use in this invention may further contain stilbene series, triazine series, oxazole series or coumarin series whitening agents in the photographic emulsion layers or other hydrophilic colloid layers thereof.
  • a whitening agent may be water-soluble, or a water-insoluble whitening agent may be used in the form of a dispersion thereof.
  • gelatin is advantageously used but other hydrophilic colloids can be used.
  • Useful gelatins include limed gelatin which is most generally used for the purpose, as well as acid- treated gelatin and enzyme-treated gelatin as described in Bull. Soc. Sci. Phot. Japan, No. 16, p. 30 (1966). Also, hydrolyzed or enzyme-decomposition products of gelatin can also be used.
  • the photographic light-sensitive materials for use in this invention may further contain an inorganic or organic hardening agent in the photographic silver halide emulsion layers and other optional hydrophilic colloid layers constituting, for example, backing layers.
  • the photographic light-sensitive materials for use in this invention may further contain at least one kind of surface active agent as a coating aid or for preventing electrification, improving the slipping property, improving emulsification- dispersibility, preventing adhesion, and improving Photographic properties (e.g., acceleration of development, increase of contrast, and increase of sensitivity).
  • the photographic light-sensitive materials for use in this invention may further contain various additives useful for photographic materials, such as various stabilizers, stain-preventing agents, developing agents or precursors therefor, development accelerators or precursors therefor, lubricants, mordants, matting agents, antistatic agents, plasticizers, etc., in addition to the above-described additives.
  • additives useful for photographic materials such as various stabilizers, stain-preventing agents, developing agents or precursors therefor, development accelerators or precursors therefor, lubricants, mordants, matting agents, antistatic agents, plasticizers, etc.
  • This invention can be applied to multilayer multicolor photographic materials having at least two silver halide emulsion layers, each having a different spectral sensitivity, on a support.
  • a multilayer natural color photographic material usually has at least one red-sensitive emulsion layer, at least one green-sensitive emulsion layer, and at least one blue-sensitive emulsion layer on a support.
  • the disposition order of these emulsion layers can optionally be selected according to the intended purpose.
  • each of the emulsion layers described above may be composed of at least two emulsion layers, each having a different sensitivity, and a light- insensitive layer may exist between two or more emulsion layers each having the same sensitivity.
  • the photographic light-sensitive material for use in this invention have a protective layer, interlayers, a filter layer, an antihalation layer, a backing layer, etc., in addition to the above-described silver halide emulsion layers.
  • the photographic light-sensitive material for use in this invention is prepared by forming the photographic emulsion layers and other layers on a flexible support of a type which is usually used for photographic materials, such as a plastic film, a paper, a cloth, etc., of a solid support such as a glass plate, porcelain, a metal foil, etc.
  • the processing process of this invention can be applied for processing general silver halide color photographic materials such as color negative photographic films, color photographic papers, color positive photographic films, color reversal films, etc., but is particularly preferably applied for processing color photographic papers.
  • a multilayer silver halide photographic material was prepared by forming the following layer 1 (the lowermost layer) to layer 7 (the uppermost layer) on a paper support, both of the surfaces of which were laminated with polyethylene.
  • the coating composition for Layer 1 described above was prepared as follows. That is, 100 g of the yellow coupler Y-l having the structure shown below was dissolved in a mixture of 166.7 ml of dibutyl phthalate (DBP) and 200 ml of ethyl acetate, the solution was dispersed by emulsification in 800 g of a 10% aqueous gelatin solution containing 80 ml of an aqueous solution of 1% sodium dodecylbenzenesulfonate, and the emulsified dispersion was mixed with 1450 g (containing 66.7 g of silver) of a blue-sensitive silver chlorobromide emulsion (Br: 80 ml % of halide content) to provide the coating composition.
  • DBP dibutyl phthalate
  • compositions for other layers described above were also prepared by similar manner to above.
  • the following dyes were used as anti-irradiation dyes.
  • Anti-irradiation dye for green-sensitive emulsion layer
  • Anti-irradiation dye for red-sensitive emulsion layer
  • the silver chlorobromide grains used for the above-described emulsion layers in this example are shown in Table 1 below.
  • Each of the photographic silver halide materials thus prepared was light-exposed through an optical wedge and then processed in the following steps.
  • compositions of the processing solutions are as follows.
  • samples 203 to 205 using the silver halide emulsions containing the tabular silver halide grains in this invention showed less dependence on the concentration of benzyl alcohol in the color developers, as in the case of Example 1.
  • a multilayer color photographic paper was prepared by forming the layers 1 to 7 having the following coating compsitions on paper support, both of the surfaces of which were laminated with polyethylene.
  • white pigment TiO 2
  • bluing dye ultramarine blue
  • the coating composition for the first layer described above was prepared as follows. That is, 19.1 g of the yellow coupler (a) shown below and 4.4 g of the color image stabilizer (b) shown below were dissolved in a mixture of 27.2 ml of ethyl acetate and 7.9 ml of the solvent (c) shown below. The resulting solution was dispersed by emulsification in 185 mt of 10% aqueous gelatin solution containing 8 ml of 10% sodium dodecylbenzenesulfonate.
  • the sensitizing dye shown below for blue-sensitive emulsion layer was added to the silver chlorobromide emulsion (silver bromide: 1.0 mole%, containing 70 g/kg of silver) in an amount of 5.0 x 10 -4 mole per 1 mole of silver chlorobromide to provide 90 g of the blue-sensitive emulsion.
  • the above emulsified dispersion was mixed with the above emulsion, and the gelatin density in the mixed solution was adjusted so as to obtain the coating compositions shown above.
  • the coating compositions for the other second to seventh layers were also prepared in the same manner as in the above first layer coating composition.
  • 1-oxy-3,5-dichloro-s-triazine sodium salt was used as a hardening agent.
  • the following dyes were used as anti-irradiation dyes.
  • Anti-irradiation dye for green-sensitive emulsion layer Anti-irradiation dye for red-sensitive emulsion layer:
  • Each of six color photographic papers thus prepared was light-exposed through an optical wedge and then processed in the following steps.
  • compositions of the processing solutions are as follows.
  • the color photographic materials were prepared in the same procedure as in Example 3 except that the yellow, magenta, and cyan.couplers shown below were used in place of the couplers in Example 3. As a result, according to the present invention, good photographic performance can be obtained.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
EP19860110788 1985-08-05 1986-08-04 Verfahren zur Behandlung farbphotographischer Silberhalogenidmaterialien Expired - Lifetime EP0211437B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP60172015A JPH0650381B2 (ja) 1985-08-05 1985-08-05 ハロゲン化銀カラ−感光材料の処理方法
JP172015/85 1985-08-05

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EP0211437A2 true EP0211437A2 (de) 1987-02-25
EP0211437A3 EP0211437A3 (en) 1989-03-15
EP0211437B1 EP0211437B1 (de) 1993-11-10

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DE (1) DE3689275T2 (de)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4745047A (en) * 1986-01-24 1988-05-17 Fuji Photo Film Co., Ltd. Color image-forming process
US4774167A (en) * 1986-02-24 1988-09-27 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic materials wherein the color developer contains low concentrations of benzyl alcohol, hydroxylamine and sulfite
US4774168A (en) * 1986-01-24 1988-09-27 Fuji Photo Film Co., Ltd. Method for forming color image with a color developer not containing benzyl alcohol
US4837132A (en) * 1986-05-23 1989-06-06 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic material using a chelating agent and developer with substantially no benzyl alcohol
US4840878A (en) * 1986-01-23 1989-06-20 Fuji Photo Film Co., Ltd. Method of color image formation using a high chloride emulsion and a developer free of benzyl alcohol
US4845016A (en) * 1986-01-29 1989-07-04 Fuji Photo Film Co., Ltd. Process for processing silver halide color photographic materials using a multistage counterflow stabilization system
US4851326A (en) * 1986-02-24 1989-07-25 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic materials using developer substantially free of bromide and benzyl alcohol
US4853318A (en) * 1986-02-17 1989-08-01 Fuji Photo Film Co., Ltd. Process for processing silver halide color photographic material using a developer comprising substantially no benzyl alcohol
US4853321A (en) * 1986-05-19 1989-08-01 Fuji Photo Film, Co., Ltd. Method of forming a color image and silver halide color photographic material using developer with substantially no benzyl alcohol and low bromide concentration
US4892803A (en) * 1986-01-23 1990-01-09 Fuji Photo Film Co., Ltd. Color image-forming process compressing developer containing no benzyl alcohol
EP0312984A3 (en) * 1987-10-19 1990-03-21 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic material
US4920042A (en) * 1986-02-20 1990-04-24 Fuji Photo Film Co., Ltd. Color image forming process comprising developing with substantially no benzyl alcohol a material having specific sensitizing dyes
EP0330093A3 (en) * 1988-02-19 1990-07-18 Fuji Photo Film Co., Ltd. Process for processing silver halide color photographic material
US5001041A (en) * 1986-01-27 1991-03-19 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic material for prints
EP0258288B1 (de) * 1986-01-24 1991-05-08 Eastman Kodak Company Photographische farbentwicklungszubereitungen zur verwendung insbesondere bei photographischen elementen mit hohem chloridgehalt
US5110713A (en) * 1987-10-30 1992-05-05 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic material
US5118593A (en) * 1986-01-29 1992-06-02 Fuji Photo Film Co., Ltd. Method for color image formation
US8063047B2 (en) 2004-11-02 2011-11-22 Centre National De La Recherche Scientifique (Cnrs) Pyridazine compounds and methods
US8158627B2 (en) 2006-04-28 2012-04-17 Northwestern University Compositions and treatments using pyridazine compounds and cholinesterase inhibitors
US8367672B2 (en) 2004-11-02 2013-02-05 Universite De Strasbourg Pyridazine compounds, compositions and methods

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JPS63250647A (ja) * 1987-04-07 1988-10-18 Konica Corp ハロゲン化銀写真感光材料の処理方法

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FR2449905A1 (fr) * 1979-02-22 1980-09-19 Hunt Chem Corp Philip A Bain et procede de traitement de films rapides notamment pour actualites televisees
JPS5674247A (en) * 1979-11-22 1981-06-19 Konishiroku Photo Ind Co Ltd Method for continuously processing silver halide photographic material
US4414306A (en) * 1981-11-12 1983-11-08 Eastman Kodak Company Silver chlorobromide emulsions and processes for their preparation
US4400463A (en) * 1981-11-12 1983-08-23 Eastman Kodak Company Silver chloride emulsions of modified crystal habit and processes for their preparation
JPS58111935A (ja) * 1981-11-12 1983-07-04 イ−ストマン・コダツク・カンパニ− 放射線感応性写真乳剤
CA1210626A (en) * 1982-12-20 1986-09-02 Gary L. House Multicolor photographic elements containing silver iodide grains
JPS6055340A (ja) * 1983-09-06 1985-03-30 Fuji Photo Film Co Ltd ハロゲン化銀カラ−感光材料
JPS60158448A (ja) * 1984-01-26 1985-08-19 Konishiroku Photo Ind Co Ltd ハロゲン化銀カラ−写真感光材料の処理方法
US4707434A (en) * 1984-08-20 1987-11-17 Konishiroku Photo Industry Co., Ltd. Color image forming method comprising processing with a bleach-fixing solution

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4840878A (en) * 1986-01-23 1989-06-20 Fuji Photo Film Co., Ltd. Method of color image formation using a high chloride emulsion and a developer free of benzyl alcohol
US4892803A (en) * 1986-01-23 1990-01-09 Fuji Photo Film Co., Ltd. Color image-forming process compressing developer containing no benzyl alcohol
US4745047A (en) * 1986-01-24 1988-05-17 Fuji Photo Film Co., Ltd. Color image-forming process
US4774168A (en) * 1986-01-24 1988-09-27 Fuji Photo Film Co., Ltd. Method for forming color image with a color developer not containing benzyl alcohol
EP0258288B1 (de) * 1986-01-24 1991-05-08 Eastman Kodak Company Photographische farbentwicklungszubereitungen zur verwendung insbesondere bei photographischen elementen mit hohem chloridgehalt
US5001041A (en) * 1986-01-27 1991-03-19 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic material for prints
US4845016A (en) * 1986-01-29 1989-07-04 Fuji Photo Film Co., Ltd. Process for processing silver halide color photographic materials using a multistage counterflow stabilization system
US5118593A (en) * 1986-01-29 1992-06-02 Fuji Photo Film Co., Ltd. Method for color image formation
US4853318A (en) * 1986-02-17 1989-08-01 Fuji Photo Film Co., Ltd. Process for processing silver halide color photographic material using a developer comprising substantially no benzyl alcohol
US4920042A (en) * 1986-02-20 1990-04-24 Fuji Photo Film Co., Ltd. Color image forming process comprising developing with substantially no benzyl alcohol a material having specific sensitizing dyes
US4851326A (en) * 1986-02-24 1989-07-25 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic materials using developer substantially free of bromide and benzyl alcohol
US4774167A (en) * 1986-02-24 1988-09-27 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic materials wherein the color developer contains low concentrations of benzyl alcohol, hydroxylamine and sulfite
US4853321A (en) * 1986-05-19 1989-08-01 Fuji Photo Film, Co., Ltd. Method of forming a color image and silver halide color photographic material using developer with substantially no benzyl alcohol and low bromide concentration
US4837132A (en) * 1986-05-23 1989-06-06 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic material using a chelating agent and developer with substantially no benzyl alcohol
EP0312984A3 (en) * 1987-10-19 1990-03-21 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic material
US5077180A (en) * 1987-10-19 1991-12-31 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic material
US5110713A (en) * 1987-10-30 1992-05-05 Fuji Photo Film Co., Ltd. Method for processing silver halide color photographic material
EP0330093A3 (en) * 1988-02-19 1990-07-18 Fuji Photo Film Co., Ltd. Process for processing silver halide color photographic material
US5380624A (en) * 1988-02-19 1995-01-10 Fuji Photo Film Co., Ltd. Process for processing silver halide color photographic material
US8063047B2 (en) 2004-11-02 2011-11-22 Centre National De La Recherche Scientifique (Cnrs) Pyridazine compounds and methods
US8367672B2 (en) 2004-11-02 2013-02-05 Universite De Strasbourg Pyridazine compounds, compositions and methods
US8933076B2 (en) 2004-11-02 2015-01-13 Centre National De La Recherche Scientifique (Cnrs) Pyridazine compounds, compositions and methods
US9527819B2 (en) 2004-11-02 2016-12-27 Northwestern University Pyridazine compounds, compositions and methods
US9663493B2 (en) 2004-11-02 2017-05-30 Northwestern University Pyridazine compounds, compositions and methods
US8158627B2 (en) 2006-04-28 2012-04-17 Northwestern University Compositions and treatments using pyridazine compounds and cholinesterase inhibitors

Also Published As

Publication number Publication date
DE3689275D1 (de) 1993-12-16
DE3689275T2 (de) 1994-02-24
JPH0650381B2 (ja) 1994-06-29
EP0211437B1 (de) 1993-11-10
JPS6232456A (ja) 1987-02-12
EP0211437A3 (en) 1989-03-15

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