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

Definitions

• This invention relates to a negative type light-sensitive silver halide photographic material.
• An object of the present invention is to provide a negative type light-sensitive silver halide photographic material which can solve the above-mentioned problems, namely capable of developing sufficient amount of silver without waste within a short time, and having an image of high contrast.
• a negative type light-sensitive silver halide photographic material comprising at least one light-sensitive silver halide emulsion provided on a support, wherein the ratio of silver amount to gelatin amount (Ag/Gel) (wherein said silver amount is the total silver amount in one or more layers provided in the same side as said light-sensitive silver halide emulsion layer with respect to the support, and said gelatin amount is the total gelatin amount in one or more gelatin layers provided in the same side as said light-sensitive silver halide emulsion layer with respect to the support) is 1.0 or more, and a hydrophilic colloid layer in said light-sensitive silver halide emulsion contains a hydrazine compound.
• the light-sensitive silver halide photographic material should contain 2 g/m 2 or less, more preferably 0.2 to 1.5 g/m 2 of a polymer latex therein.
• the present inventors have found that in order to obtain sufficient density after development processing by ultra-fast processing,increase of Ag/Gel should be extremely preferable rather than mere increase of the silver amount coated, to have accomplished the above invention.
• increase of Ag/Gel should be extremely preferable rather than mere increase of the silver amount coated, to have accomplished the above invention.
• by merely increasing Ag/Gel there is a tendency that cracking may occur when the raw film and the film after processing is stored under low humidity conditions (at relative humidity of 30 % or lower) during storage, and hence it has been found that a polymer latex of 2 g/m 2 or lower should be desirably contained in the light-sensitive silver halide photographic material. Also, by doing so, the problem of coating irregularity has been improved.
• the gelatin amount in the present invention is the sum of the gelatin amount in the gelatin layers of one layer or more in the side including the light-sensitive silver halide emulsion layer with respect to the support (even in the case of the gelatin derivative as described below, the amount of the gelatin derivative is considered as the gelatin amount), and is not limited only to the gelatin amount in the silver halide emulsion layer. Also, the silver amount is the total silver amount in the respective layers, when it is provided by coating in a plural number of layers in the same side with respect to the support.
• the hydrazine compound to be used in the present invention may include compounds represented by the following formula [I], [I-a], [I-b] or [I-c]. wherein R 1 and R 2 each represent hydrogen atom, a monovalent aromatic residue, a monovalent heterocyclic residue or a monovalent aliphatic residue, Q 1 and Q 2 each represent hydrogen atom, an alkylsulfonyl group which may be substituted or unsubstituted, an arylsulfonyl group which may be substituted or unsubstituted, and X 1 represents oxygen atom or sulfur atom.
• R 1 and R 2 each represent an aryl group or a heterocyclic group
• R represents a divalent organic linking group
• n is 0 to 6
• m is 0 or 1
• respective R's may be either the same or different.
• R 21 represents an aliphatic group, an aromatic group or a heterocyclic group
• R 22 represents hydrogen atom, an alkoxy group which may be substituted, a heterocyclic oxy group, an amino group or an aryloxy group
• P 1 and P 2 each represent hydrogen atom, an acyl group or a sulfinic acid group.
• Ar represents an aryl group containing at least one of diffusion resisitant group or silver halide adsorption promoting group
• R 3 represents a substituted alkyl group.
• hydrazine compounds represented by Formula [I] to be used in the present invention the compounds wherein X, is oxygen atom and R 2 is hydrogen atom are particularly preferred.
• aromatic residues there may be included phenyl group, naphthyl group and these groups having substituents (e.g. alkyl, alkoxy, acylhydrazino, dialkylamino, alkoxycarbonyl, cyanol, carboxyl, nitro, alkylthio, hydroxy, sulfonyl, carbamoyl groups, halogen atoms, acylamino, sulfonamide, thiourea groups, etc.).
• substituents e.g. alkyl, alkoxy, acylhydrazino, dialkylamino, alkoxycarbonyl, cyanol, carboxyl, nitro, alkylthio, hydroxy, sulfonyl, carbamoyl groups, halogen atoms, acylamino, sulfonamide, thiourea groups, etc.
• substituents may include 4-methylphenyl, 4- ethylphenyl, 4-oxyethylphenyl, 4-dodecylphenyl, 4-carboxyphenyl, 4-diethylaminophenyl, 4-octylaminophenyl, 4-benzylaminophenyl, 4-acetamido-2-methylphenyl, 4-(3-ethylthioureido)phenyl, 4-[2-(2,4-di-tert-butylphenoxy)butylamido]phenyl, 4-[2-(2,4-di-tert-butylphenoxy)butylamido]phenyl groups, etc.
• heterocyclic groups 5-membered or 6-membered monocyclic or fused rings having at least one of oxygen, nitrogen, sulfur or selenium atom may be included, and these may have substituents.
• specific examples may include residues such as pyrroline, pyridine, quinoline, indole, oxazole, benzooxazole, naphthoxazole, imidazole, benzoimidazole, thiazoline, thiazole, benzothiazole, naphthothiazole, selenazole, benzoselenazole, naphthoselenazole rings, etc.
• heterocyclic rings may be also substituted with alkyl groups having 1 to 4 carbon atoms, alkoxy groups having 1 to 4 carbon atoms, aryl group having 6 to 18 carbon atoms, halogen atoms, alkoxycarbonyl group, cyano group, amide group, etc.
• Examples of the straight or branched alkyl group may include alkyl groups having 1 to 18, preferably 1 to 8 carbon atoms, specifically methyl, ethyl, isobutyl, 1-octyl groups and the like.
• Examples of the cycloalkyl group may include those having 3 to 10 carbon atoms, specifically cyclopropyl, cyclohexyl, adamantyl groups and the like.
• substituent on the alkyl group or the cycloalkyl group there may be included alkoxy, alkoxycarbonyl, carbamoyl, hydroxy, alkylthio, amide, acyloxy, cyano, sulfonyl groups, halogen atoms, aryl groups, etc., and specific examples of those substituted can include 3-methoxypropyl, ethoxycarbonylmethyl, 4-chlorocyclohexyl, benzyl, p-methylbenzyl, p-chlorobenzyl groups, etc.
• alkenyl group for example, allyl group, and as the alkynyl group, propargyl group may be included.
• R, and R 2 each represent an aryl group or a heterocyclic group, R represents a divalent organic linking group, and n represents 0 to 6 and m represents 0 or 1.
• the aryl group represented by R, and R 2 may include phenyl group, naphthyl group, and the heterocyclic group represented by R 1 and R 2 may include pyridyl group, benzothiazolyl group, quinolyl group, thienyl group, etc., but R, and R 2 may be preferably aryl groups.
• the aryl group or heterocyclic group represented by R 1 and R 2 can introduce various substituents therein. Examples of substitutents may include halogen atoms (e.g. chlorine, fluorine, etc.), alkyl groups (e.g. methyl, ethyl, dodecyl, etc.), alkoxy groups (e.g.
• acylamino groups ⁇ e.g. acetylamino, pivalylamino, benzoylamino, tetradecanoylamino, a-(2,4-di-t-amylphenoxy) butyrylamino, etc. ⁇ , sulfonylamino groups (e.g. methanesulfonylamino, butanesulfonylamino, dodecanesulfonylamino, ben- zenesulfonylamino, etc.), urea groups (e.g.
• phenylurea, ethylurea, etc. thiourea groups (e.g. phenylthiourea, ethylthiourea, etc.), hydroxy group, amino group, alkylamino groups (e.g. methylamino, dimethylamino, etc.), carboxy group, alkoxycarbonyl groups (e.g. ethoxycarbonyl), carbamoyl group, sulfo group and so on.
• Examples of the divalent organic linking group represented by R may include alkylene groups (e.g. methylene, ethylene, trimethylene, tetramethylene, etc.), arylene groups (e.g.
• phenylene, naphthylene, etc. aralkylene groups, etc.
• the alkylene group may contain oxy group, thio group,seleno group, carbonyl group, group (R 3 represents hydrogen atom, an alkyl group, an aryl group), sulfonyl group, etc. in the bond.
• R 3 represents hydrogen atom, an alkyl group, an aryl group
• sulfonyl group etc. in the bond.
• Into the group represented by R can be introduced various substituents.
• substituents may include -CONHNHR 4 (R 4 has the same meaning as R 1 and R 2 as described above), alkyl groups, alkoxy groups, halogen atoms, hydroxy group, carboxy group, acyl groups, aryl groups, etc.
• R may be preferably a alkylene group.
• the aliphatic group represented by R 21 may be preferably one having 6 or more carbon atoms, particularly a straight, branched or cyclic alkyl group having 8 to 50 carbon atoms.
• the branched alkyl group may be cyclized so as to form a saturated hetero ring containing one or more hetero atoms.
• the alkyl group may have substituent such as aryl group, alkoxy group, sulfoxy group, etc.
• the aromatic group represented by R 21 is a monocyclic or bicyclic aryl group or unsaturated heterocyclic group.
• the unsaturated heterocyclic group may be condensed with the monocyclic or bicyclic group to form a heteroaryl group.
• benzene ring there may be included benzene ring, naphthalene ring, pyridine ring, pyrimidine group, imidazole ring, pyrazole ring, quinoline ring, isoquinoline ring, benzimidazole ring, thiazole ring, benzothiazole ring, etc., but amount them those containing benzene ring are preferred.
• R 21 particularly preferred is an aryl group.
• the aryl group or unsaturated heterocyclic group represented by R 21 may be substituted, and representative substituents may include straight, branched or cyclic alkyl groups (preferably monocyclic or bicyclic ones with an alkyl moiety having 1 to 20 carbon atoms), alkoxy groups (having preferably 1 to 20 carbon atoms), substituted amino groups (preferably amino groups substituted with alkyl groups having 1 to 20 carbon atoms), acylamino groups (having preferably 2 to 30 carbon atoms), sulfonamide groups (having preferably 1 to 30 carbon atoms), ureido groups (having preferably 1 to 30 carbon atoms) and others.
• substituents may include straight, branched or cyclic alkyl groups (preferably monocyclic or bicyclic ones with an alkyl moiety having 1 to 20 carbon atoms), alkoxy groups (having preferably 1 to 20 carbon atoms), substituted amino groups (preferably amino groups substituted with alkyl groups having 1 to 20 carbon
• the alkoxy group which may be substituted may have 1 to 20 carbon atoms and may be substituted with halogen atoms, aryl groups, etc.
• the aryloxy group or the heterocyclic oxy group which may be also substituted may be preferably monocyclic, and the substituent may include halogen atoms, alkyl groups, alkoxy group, cyano group, etc.
• R 22 Of the groups represented by R 22 , preferably are alkoxy groups or amino groups which may be also substituted.
• a 1 and A 2 in the group group may be an alkyl group, alkoxy group which may be substituted, or a cyclic structure containing -0-, -S-, -N- group bond.
• R 22 cannot be hydrazino group.
• R 21 or R 22 in Formula [I - b] may be one having a ballast group conventionally used in the immobile additive for photography such as coupler, etc. incorporated therein.
• the ballast group is a group having 8 or more carbon atoms relatively inert to photographic characteristic, and can be chosen from, for example, alkyl groups, alkoxy groups, phenyl groups, alkylphenyl groups, phenoxy groups, alkylphenoxy groups, etc.
• R 21 or R 22 in Formula [I - b] may be also one having a group for strengthening adsorption ot the surface of silver halide grains incorporated therein.
• adsorptive groups there may be included the groups as disclosed in U.S. Patent 4,355,105 such as thiourea group, heterocycic thioamide group, mercaptoheterocyclic group, triazole group, etc.
• the compounds represented by the group [I - b] are particularly preferable.
• Ar represents an aryl group containing at least one of diffusion resistant groups or silver halide adsorption promoting groups, and as the diffusion resistant group, a ballast group conventionally used in immobile additives for photogrpahy such as coupler etc. is preferable.
• the ballast group is a group having 8 or more carbon atoms relatively inert to photographic characteristic, and can be chosen from, for example, alkyl groups, alkoxy groups, phenyl groups, alkylphenyl groups, phenoxy groups, alkylphenoxy groups, etc.
• silver halide adsorption promoting group there may be included the groups as disclosed in U.S. Patent 4,385,108 such as thiourea group, thiourethane group, heterocyclic thioamide group, mercaptoheterocyclic group, triazole group, etc.
• R 3 represents a substituted alkyl group, and the alkyl group may be a straight, branched or cyclic alkyl group, including methyl, ethyl, propyl, butyl, isopropyl, pentyl, cyclohexyl and the like.
• alkoxy e.g. methoxy, ethoxy
• aryloxy e.g. phenoxy, p-chlorophenoxy
• heterocyclic oxy e.g. pyridyloxy
• alkylthio e.g. metylthio, ethylthio
• arylthio e.g. phenylthio, p-chlorophenylthio
• heterocyclic thio e.g. pyridylthio, pyrimidylthio, thiadiazolylthio
• alkylsulfonyl e.g.
• acetyloxy acetyloxy, benzoyloxy
• alkylaminocarbonyloxy e.g. methylaminocarbonyloxy
• arylaminocar- bonyloxy e.g. phenylaminocarbonyloxy
• sulfo sulfamoyl
• alkylsulfamoyl e.g. methylsulfamoyl
• arylsulfamoyl e.g. phenylsulfamoyl
• the hydrogen atom of hydrazide may be also substituted with a substituent such as sulfonyl gorup (e.g. methanesulfonyl, toluenesulfonyl), acyl group (e.g. acetyl, trifluoroacetyl), oxalyl group (e.g. ethoxalyl), etc.
• sulfonyl gorup e.g. methanesulfonyl, toluenesulfonyl
• acyl group e.g. acetyl, trifluoroacetyl
• oxalyl group e.g. ethoxalyl
• the position where the above hydrazine compound is to be added is in the silver halide emulsion layer and/or the non-light-sensitive layer existing on the silver halide emulsion layer on the support, but preferably in the silver halide emulsion layer and/or its subbing layer.
• the amount added should be preferably 10- 5 to 10 -1 mole/ 1 mole of silver, further preferably 10- 4 to 10- 2 mole/1 mole of silver.
• the average grain size refers to its diameter in the case of spherical particles, or the diameter when calculated on the circular image with the same area as its projected image in the case of grains with shapes other than spherical shape.
• 60 % or more of the total grains should have particle sizes within the range of ⁇ 10% of the average grain size.
• silver halide emulsion to be used in the present invention (hereinafter called silver halide emulsion or merely emulsion)
• any of silver bromide, silver iodobromide, silver iodochloride, silver chloroiodobromide, silver chloride, silver chlorobromide, silver iodide may be used.
• the silver halide emulsion used in the present invention may have a single composition, or alternatively grains with a plurality of compositions may be also contained within the single layer or a plurality of layers.
• metal ions by use of at least one selected from cadmium salts, zinc salts, lead salts, thallium salts, iridium salts (complexes containing them), rhodium salts (complexes containing them) and iron salts (complexes containing them) in the process of forming and/or growing the grains to incorporate these metal elements internally of the grains and/or on the grain surfaces, and a water-soluble rhodium salt is particularly preferably. Also, by placing in a reductive appropriate atmosphere, reduced sensitizing nuclei can be imparted internally of the grains and/or on the grain surfaces. When a water-soluble rhodium salt is added, the amount added may be preferably 1 x 10- 7 to 1 x 10- 4 mole/1 mole AgX.
• the silver halide grains to be used in the silver halide emulsion may either have a uniform silver halide composition distribution within the grain or a core-shell grain with different silver halide compositions in the inner portion and in the surface layer of the grain.
• the silver halide grains to be used in the silver halide emulsion may be either those in which latent images are formed primarily on the surface or those primarily internally of the grains.
• the silver halide grains to be used in the silver halide emulsion may be either those having regular crystal forms such as cubic, octahedral, tetradecahedral bodies, or irregular shapes such as spherical, plate shapes. Also, they may have composite form of these crystal forms, and may contain grains of various forms mixed therein.
• silver halide emulsion two or more kinds of silver halide emulsions which.have been formed separately may be used in a mixture.
• the silver halide emulsion should be preferably sensitized by use of chemical sensitizers and the sensitizing methods as described in G.B. Patent Nos. 618,061, 1,315,755, 1,396,696, Japanese Patent Publication No. 15748/1969, U. S. Patent Nos.
• the silver halide emulsion to be used in the light-sensitive material according to the present invention can be chemically sensitized to a required wavelength region by use of a dye which has been known as the sensitizing dye in the field of photography.
• the sensitizing dye may be also used alone, but may be also used in combination of two or more kinds. Together with the sensitizing dye, there may be also contained a supersensitizer which is a dye having itself no spectral sensitizing action, or a compound absorbing substantially no visible light, and potentiating the sensitizing action of the sensitizing dye may be also contained in the emulsion.
• the useful sensitizing dye to be used in the blue-sensitive silver halide nucleus emulsion layer there may be included, for example, those as described in West German Patent No. 929,080, U. S. Patent Nos. 2,231,658, 2,493,748, 2,503,776, 2,519,001, 2,912,329, 2,656,959, 3,672,897, 3,694,217, 4,025,349, 4,046,572, G. B. Patent No. 1,242,588, Japanese Patent Publication Nos. 14030/1969, 24844/1977.
• the useful sensitizing dye to be used in the green- sensitive silver halide emulsion there may be included, for example, cyanine dyes, melocyanine dyes or complex cyanine dyes as described in U. S. Patent Nos. 1,939,201, 2,072,908, 2,739,149, 2,945,763, G. B. Patent No. 505,979 as representative ones.
• the useful sensitizing dye to be used in the red-sensitive silver halide emulsion there may be included, for example, cyanine dyes, melocyanine dyes or complex cyanine dyes as described in U. 5.
• Patent Nos. 2,269,234, 2,270,378, 2,442,710, 2,454,629, 2,776,280 as representative ones.
• cyanine dyes or complex cyanine dyes as described in U. S. Patent Nos. 2,213,995, 2,493,748, 2,519,001, West German Patent No. 929,080 can be advantageously used in the green-sensitive silver halide emulsion or the red-sensitive silver halide emulsion.
• a compound known as the antifoggant or stabilizer in the field of photography can be added during chemical aging, on completion of chemical aging and/or after completion of chemical aging before coating of the silver halide emulsion.
• antifoggant, stabilizer may include azaindenes such as pentazaindenes as disclosed in U. S. Patent Nos. 2,713,541, 2,743,180, 2,743,181, tetrazaindenes as disclosed in.U. S. Patent Nos. 2,716,062, 2,444,607, 2,444,605, 2,756,147, 2,835,581, 2,852,375, Research Disclosure 14851, triazaindenes as disclosed in.U. S. Patent No. 2,772,146, polymerized azaindenes as disclosed in.Japanese Unexamined Patent Publication No. 211142/1982; quaternary phosphonium salts such as thiazolium salts as disclosed in.U.
• heterocyclic compounds including azoles such as tetrazoles as disclosed in.West German Patent No. 1,189,380, triazole as disclosed in.U. S. Patent No. 3,157,509, benztriazoles as disclosed in U. S. Patent No. 2,704,721, urazoles as disclosed in.U. S. Patent No. 3,287,135, pyrazoles as disclosed in U. S. Patent No. 3,106,467, imidazoles as disclosed in.U. S. Patent No. 2,271,229, and azoles such as polymerized benzotriazoles as disclosed in.Japanese Unexamined Patent Publication No. 90844/1984, etc., pyrimidines as disclosed in U. S.
• hydrophilic colloid layers in the light-sensitive material to be used in the present invention various additives for photography can be used, if necessary, such as gelatin plasticizers, film hardeners, surfactants, image stabilizers, UV-ray absorbers, antistain agents, pH controllers, antioxidants, antistatic agents, thickeners, graininess improvers, dyes, mordants, brighteners, developing speed controllers, matte agents, etc., within the range which does not impair the effect of the present invention.
• a polymer latex should be preferably contained, and examples of the polymer latex to be incorporated in said light-sensitive material may include preferably hydrates of vinyl polymers such as acrylates, methacrylates, styrene, etc. as disclosed in U. S. Patent Nos. 2,772,166, 3,325,286, 3,411,911, 3,311,912, 3,525,620, Research Disclosure No. 195, 19551 published in July, 1989.
• polymer latex which may be preferably used, there may be included homopolymers of methaalkyl acrylate such as methyl methacryate, ethyl methacrylate, etc, homopolymers of styrene, or copolymers of methaalkyl acrylate or styrene with acrylic acid, N-methylolacryl-amide, glycidol methacrylate, etc., homopolymers of alkyl acrylate such as methyl acrylate, ethyl acrylate, butyl acrylate, etc. or copolymers of alkyl acrylate with acrylic acid, N-methylolacrylamide, etc.
• methaalkyl acrylate such as methyl methacryate, ethyl methacrylate, etc
• homopolymers of styrene or copolymers of methaalkyl acrylate or styrene with acrylic acid, N-methylolacryl
• the content of the copolymer component such as acrylic acid, etc. being up to 30 % by weight
• the preferable range of the average particle size of the polymer latex to be used in the present invention may be 0.005 to 1 ⁇ , particularly preferably 0.2 to 0.1 ⁇ .
• the polymer latex to be used in the present invention may be contained either on one surface with respect to the support or both surfaces. More preferably, it should be contained on both surfaces. When it is contained on both surfaces with respect to the support, the kind and/or the amount of the polymer latex contained on the respective surfaces may be either the same or different.
• the layer in which the polymer latex is added may be any layer.
• the polymer latex when it is contained in the side containing the silver halide light-sensitive layer with respect to the support, the polymer latex may be contained in the silver halide light-sensitive layer, or altrnatively in the non-light-sensitive colloid layer of the uppermost layer which is generally called protective layer.
• the polymer latex may be contained in either single layer in the surface comprising a plurality of layers or in plural layers (not limited to 2 layers) comprising any desired combination of layers.
• gelatin As the binder in the light-sensitive material to be used in the present invention, gelatin is used, and this gelatin includes gelatin derivatives, etc., and also cellulose derivative , graft polymers of gelatin with other polymers, and other proteins, sugar derivatives, cellulose derivatives, hydrophilic colloids of synthetic hydrophilic polymeric substances, etc. which may be either of homopolymers or copolymers can be also used in combination.
• gelatin in addition to lime-treated gelatin, acid-treated gelatin, enzyme-treated gelatin as described in Bulletin of Society of Science Photography of Japan (Bull. Soi. Sci. Phot. Japan) No. 16, p. 30 (1966) may be also used, and also hydrolyzates or enzyme decomposed products of gelatin can be used.
• gelatin derivatives there may be employed those obtained by reacting various compounds such as acid halide, acid anhydride, isocyanates, bromoacetic acid, alkanesulfones, vinylsulfonamides, maleinimide compounds, polyalkylene oxides, epoxy compounds, etc. with gelatin. Specific examples are disclosed in U. S. Patent Nos. 2,614,928, 3,132,945, 3,186,846, 3,312,553, Nos. 861,414, 1,033,189 1,005,784, Japanese Patent Publication No. 26845/1967.
• albumin As the protein, albumin, casein, as the cellulose derivative, hydroxyethyl cellulose, carboxymethyl cellulose, cellulose sulphate or as the sugar derivative, sodium alginate, starch derivative may be also used in combination with gelatin.
• graft polymer of gelatin with other polymers those having homo- or copolymer of a vinyl type monomer such as acrylic acid, methacrylic acid, derivatives thereof such as ester, amide, etc., acrylonitrile, styrene, etc. grafted onto gelatin can be used.
• graft copolymers of polymers compatibility to some extent with gelatin such as polymers of acrylic acid, acrylamide, methacrylamide, hydroxyalkyl methacrylate, etc. are preferred. Examples of these are disclosed in U. S. Patent Nos. 2,763,625, 2,831,767, 2,956,884.
• the amount of gelatin coated, when containing no polymer latex other than subbing layer on the surface corresponding to the surface of the light-sensitive material, may be preferably 1.8 g/m 2 to 5.5 g/m 2 , particularly 2.0 to 4.8 g/m 2 per one surface of the support.
• a polymer latex When a polymer latex is contained on that surface, it should be preferably 1.5 to 6.0 g/m 2 , particularly preferably 1.8 to 5.5 g/m 2 .
• the support to be used in the light-sensitive material of the present invention may include flexible reflective support such as papers laminated with a-olefin polymer (e.g. polyethylene/butene copolymer), etc., synthetic papers, etc., films comprising semi-synthetic or synthetic polymers such as cellulose acetate, cellulose nitrate, polystyrene, polyvinyl chloride, polyethylene terephthalate, polycarbonate, polyamide, etc., and flexible supports having reflective layer provided on these films, metal, etc.
• a-olefin polymer e.g. polyethylene/butene copolymer
• synthetic papers etc.
• films comprising semi-synthetic or synthetic polymers such as cellulose acetate, cellulose nitrate, polystyrene, polyvinyl chloride, polyethylene terephthalate, polycarbonate, polyamide, etc.
• polyethylene terephthalate is particularly preferred.
• subbing layer which can be used in the present invention, there may be included the subbing working layer in organic solvent system containing polyhydroxybenzenes as disclosed in Japanese Unexamined Patent Publication No. 3972/1984, etc., aqueous latex subbing working layers as disclosed in Japanese Unexamined Patent Publication No. 11118/1974, 104913/1977, 19941/1984, 19940/1984, 18945/1984, 112326/1976, 117617/1976, 58469/1976, 114120/1976, 121323/1976, 123129/1976, 114121/1976, 139320/1977, 65422/1977, 109923/1977, 119919/1977, 65949/1980, 128332/1982, 19941/1984.
• organic solvent system containing polyhydroxybenzenes as disclosed in Japanese Unexamined Patent Publication No. 3972/1984, etc.
• aqueous latex subbing working layers as disclosed in Japanese Unexamined Patent Publication No. 11118/1974, 104913/19
• said subbing layer can be generally subjected on its surface to chemical or physical treatment.
• treatment there may be included surface activating treatments such as chemical treatment, mechanical treatment, corona dicharging treatment, flame treatment, UV-ray treatment, high frequency treatment, glow discharging treatment, active plasma treatment, laser treatment, mixed acid treatment, ozone oxidation treatment, etc.
• the subbing layer is distinguished from the coating layer according to the present invention and the coating timing and conditions are not limited at all.
• filter dyes and other dyes for various purposes such as halation prevention can be used.
• the dyes employed may include triaryl dyes, oxanol dyes, hemioxanol dyes, malocyanine dyes, cyanine dyes, styryl dyes, azo dyes. Among them, oxanol dyes, hemioxanol dyes and melocyanine dyes are useful. Specific examples of the dyes which can be used may include those as disclosed in West German Patent No. 616,007, G. B. Patent Nos. 584,609, 1,177,429, Japanese Patent Publication Nos.
• these dyes should be preferably used, and it is particularly preferable to use them so that the sensitivity to the light of 400 nm may be incorporated to 30-fold or more of the sensitivity to the light of 360 nm.
• the light-sensitive material of the present invention can be exposed by use of an electromagnetic wave in the spectral region to which the emulsion layer constituting said light-sensitive material has sensitivity.
• the present invention can give remarkable effect when applied to a light-sensitive material for printing for which very high dimensional stability before and after processing is required.
• the developing agent to be used in development of the light-sensitive silver halide photographic material according to the present invention may include those as mentioned below.
• 3-pyrazolidones such as 1-phenyl-3-pyrazolidone, 1-phenyl-4,4-dimethyl-3-pyrazolidone, 1-phenyl-4-methyl-4-hydroxymethyl-3-pyrazolidone; 1-phenyl-4-amino-5-pyrazolone, 5-aminouracil, etc.
• a sulfite such as sodium sulfite, potassium sulfite, etc. can be used without impairing the effect of the present invention.
• hydroxylamine, a hydrazide compound can be used as the preservative, and in this case, its amount may be preferably 5 to 500 g, more preferably 20 to 200 g per one liter of the developer.
• glycols as an organic solvent, and as such glycol, ethylene glycol, diethylene glycol, propylene glycol, triethylene glycol, 1,4-butanediol, 1,5-pentane diol, etc. may be preferably used.
• the amount of these glycols used may be 5 to 500 g, more preferably 20 to 200 g per one liter of the developer.
• These organic solvents can be used either alone or in combination.
• the light-sensitive silver halide photographic material according to the present invention can be subjected to developing processing by use of a developer containing a development inhibitor, whereby a light-sensitive material very excellent in storage stability can be obtained.
• the light-sensitive silver halide photographic material according to the present invention can be processed under various conditions.
• the processing temperature may be, for example, a developing temperature of 50 ° C or lower, particularly around 25 to 40 C, and also the developing time should be preferably completed within less than 20 seconds, particularly 19 seconds or less. Further, the present invention can exhibit its effect most effectively when the developing time is within the range of 15 seconds or less, and further 15 to 10 seconds.
• processing steps than developing, for example, water washing, stopping, stabilizing, fixing, and further previous film hardening, neutralization, etc. can be employed as desired, and these can be also suitably omitted.
• various acids, salts, fixing promoters, humectants, surfactants, chelating agents, film hardeners, etc. can be contained.
• thiosulfates, sulfites, potassium, sodium, ammonium salts of these acids as acids, sulfuric acid, hydrochloric acid, nitric acid, boric acid, formic acid, acetic acid, propionic acid, oxalic acid, tartaric acid, citric acid, malic acid, phthalic acid, etc. and as salts, potassium, sodium, ammonium salts, etc.
• thiourea derivatives examples include thiourea derivatives, alcohols having triple bond within the molecule as disclosed in.Japanese Patent Publication No. 35754/1970, Japanese Unexaned Patent Publication Nos. 122535/1983, 122536/1983, thioethers, as disclosed in U.S. Patent 4,126,459, or cyclodextran ethers which make free anions, crown ethers, diazabicycloundecene, di(hydroxyethyl)butamine, etc.
• humectant alkanolamines, alkylene glycols, etc. may be included.
• aminoacetic acids such as nitrilotriacetic acid, EDTA, etc. may be included.
• film hardener chromium alum, potassium alum, and other AI compounds, etc. can be incorporated.
• the present invention can exhibit its advantages greatly when ultra-fast processing with a processing time of 20 to seconds is applied.
• the ultra-fast processing as mentioned in the present specification refers to a processing in which the total time after the tip end of a film is inserted into an automatic developing machine, passing through the developing tank, the cross-over portion, the fixing tank, the cross-over portion, the water washing tank, the cross-over portion, the drying portion, until the tip end of the film comes out from the drying portion (in other words the quotient of the entire length of the processing line divided by the line conveying speed) is 20 seconds to 60 seconds.
• 1.2 g of the hydrazine compound shown in Table 2 was added to the emulsion A per 1 mole of silver.
• the antifoggant 30 mg/m2 of 1-phenyl-5-mercaptotetrazole and 20 mg/m 2 of 5-methylbenzotriazole
• the development controller 30 mg/m 2 of a nonylphenoxy-polyethylene glycol (ethylene oxide units 30) and 1 g/m 2 of an acrylic acid-butyl methacrylate-styrene polymer latex, and further bisvinylsul- fomethyl ether and glyoxazole of the film hardening agent were successively added, and the resultant mixture was coated on a polyethylene terephthalate base simultaneously with a protective layer.
• gelatin amount lu relative to the silver amount is shown in Table 2. Then, these samples were exposed through a glass wedge by P-627 FM roomlight printer (manufactured by Dainippon Screen), and processed with the developer and the fixer shown below. In this processing, developing time was 15 seconds (35 C).
• the above compositions A and B were dissolved in this order in 500 ml of water and then made up to one liter before use.
• the pH of the fixer was adjusted to 6 with acetic acid.
• the amount of the silver coated was analyzed by a fluorescent X-ray analyzer.
• the silver amount after processing is shown in the silver amount which gives the maximum density.
• y is defined for density from 0.3 to 3.0.
• the product with y ⁇ 6 can be practically applied with difficulty because fine lines are practically collapsed.
• Example 3 To the emulsion B subjected to gold-sulfur sensitization was added 1.2 g of the hydrazine compound shown in Table 3 and also 300 mg of the sensitizing dye shown below per one mole of silver, followed by coating similarly as in Example 1. The gelatin amount relative to the silver amount is shown in Table 3. These samples were subjected to wedge exposure by xenon light, and processed similarly as in Example 1.
• the dot quality was evaluated based on the sensory examination by enlarging the dot formed by bringing the contact screen in close dot contact with the film during exposure with a 100-fold magnifier.
• the rank 5 indicates the highest state, with the states of rank 2 or lower standing no practical application.
• Example 4 To the emulsion of C applied with gold-sulfur sensitization, 1.2 g of the hydrazine compound shown in Table 4 was added per one mole of silver, and 200 mg of the sensitizing dye shown below per one mole of silver, followed by coating similarly as in Example 1. The amount of the gelatin amount relative to the silver amount is shown in Table 4. These samples were subjected to wedge exposure by xenon light, and processed similarly as in Example 1.

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• 1988
  • 1988-11-09 JP JP63281304A patent/JPH02129626A/ja active Pending
• 1989
  • 1989-11-06 US US07/432,045 patent/USH1063H/en not_active Abandoned
  • 1989-11-07 EP EP19890120561 patent/EP0368229A3/de not_active Withdrawn
  • 1989-11-08 CA CA002002517A patent/CA2002517A1/en not_active Abandoned

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