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
  • G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
  • G03C1/85—Photosensitive materials characterised by the base or auxiliary layers characterised by antistatic additives or coatings
  • G03C1/89—Macromolecular substances therefor
• • 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
  • G03C1/38—Dispersants; Agents facilitating spreading
• • 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
  • G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
  • G03C1/85—Photosensitive materials characterised by the base or auxiliary layers characterised by antistatic additives or coatings
• • 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
  • G03C2200/00—Details
  • G03C2200/48—Polyoxyethylene

Definitions

• the present invention relates to photographic film bases which are provided with antistatic layers, and to light-sensitive photographic elements comprising said film bases.
• polyester film bases such as poly(ethylene terephthalate) or poly(ethylene naphthalate) film bases.
• polyester film bases when compared with commonly used cellulose ester film bases, are dimensionally more stable and more resistant to mechanical stresses under most conditions of use.
• photographic elements comprising light-sensitive layers coated onto polymeric film bases, when used in rolls or reels which are mechanically wound and unwound or in sheets which are conveyed at high speed, tend to accumulate static charges and record the light generated by the static discharges.
• the static-related damages may occur not only before the photographic element has been manufactured, exposed and processed, but also after processing when the photographic element including the image is used to reproduce or enlarge the image. Accordingly, it is desired to provide permanent antistatic protection, that is an antistatic protection which retains its effectiveness even after photographic processing.
• Matting agents, hygroscopic materials or electroconductive polymers have been proposed to prevent static buildup, each acting with a different mechanism.
• matting agents cause haze, dust and dirt problems
• hygroscopic materials cause sheets or films to stick together or with other surfaces
• electroconductive polymers are not permanent after photographic processing or are not transparent when coated with conventional binders.
• US 4,225,665 purports to disclose permanent antistatic layers for photographic elements. Said layers consist essentially of three components: (1) a water-soluble, electrically conductive polymer comprising carboxylic groups, (2) a hydrophobic polymeric binder containing carboxylic groups, and (3) a polyfunctional aziridine crosslinking agent. This composition, however, does not give clear coatings and causes premature reactions among the components prior to coating. US 4,701,403 suggests a costly system of coating the components as two separate coatings to avoid these premature reactions.
• US 4,585,730 discloses a photographic element comprising a film base, a silver halide emulsion on one side of the support, and an antistatic layer on the other side of said support, wherein the antistatic layer is coated with an auxiliary gelatin layer containing a conductive polymer, whereby the antistatic properties of the antistatic layer are conducted through said auxiliary layer.
• antistatic layer coated onto a polymeric film base has been described in EP 486,982.
• That antistatic layer comprises the reaction product of a copolymer of sodium polystyrene sulfonate and maleic acid (having a weight average molecular weight of 16,700) with a polyfunctional epoxide crosslinking agent.
• This antistatic layer provides good adhesion of photographic gelatin layers coated over it even during photographic processing.
• EP 589,329 describes an improvement of the above mentioned EP 486,982.
• the antistatic layer described in EP 589,329 comprises a copolymer of a water soluble salt of styrene sulfonic acid and maleic acid having a weight average molecular weight of 100,000 to 350,000 and a water soluble salt of styrene sulfonic acid to maleic acid molar ratio of at least 2:1 up to 9:1.
• the invention is directed to a polymeric film base at least one side of which is coated with an antistatic layer comprising (1) the reaction product of (a) a water-soluble, electrically conductive polymer containing carboxylic groups and (b) a polyfunctional epoxide crosslinking agent, and (2) a non-ionic perfluoroalkyl(ene)polyoxyalkylene surfactant.
• the invention is directed to a photographic element comprising a polymeric film base, a silver halide emulsion layer on said film base, and an antistatic layer which comprises (1) the reaction product of (a) a water-soluble, electrically conductive polymer containing carboxylic groups and (b) a polyfunctional epoxide crosslinking agent, and (2) a non-ionic perfluoroalkyl(ene)polyoxyalkylene surfactant.
• This antistatic layer may be present as a backing layer on the side of the film base opposite the silver halide emulsion layer, as a subbing layer between the film base and the emulsion layer in a single or double side coated photographic element, and/or as a subbing layer between the film base and a different backing layer.
• the present invention comprises an antistatic film base particularly useful for imaging media, especially silver halide photographic media.
• the film base comprises a polymeric substrate such as a polyester, and especially polyethyleneterephthalate or poly(ethylene naphthalate). Other useful polymeric substrates include cellulose acetates, polyolefins, polycarbonates and the like.
• the film base has an antistatic layer adhered to one or both major surfaces of the base.
• a primer layer or subbing layer may be used between the base itself and the antistatic layer as is known in the art. Priming and subbing layers are, in fact, generally considered to be part of the base itself unless specifically excluded in the description (e.g., unsubbed polyester). Primer and subbing compositions are well known in the art and polymers of vinylidene chloride often comprise the primer composition of choice for photographic elements.
• the antistatic layer of the present invention comprises (1) the reaction product of (a) a water-soluble electrically conductive polymer having carboxylic groups and (b) a polyfunctional epoxide crosslinking agent, and (2) a non-ionic perfluoroalkyl(ene)polyoxyalkylene surfactant.
• the component (a) of the antistatic layer of the present invention is preferably a water-soluble (e.g., soluble in water at room temperature for at least 5% in weight, preferably for at least 10%) electrically conductive hydrophilic copolymer having monomer units comprising:
• the component (a) is a copolymer of a styrene sulfonate and an ethylenically unsaturated comonomer containing carboxylic groups.
• the component (a) is a copolymer of sodium styrene sulfonate and maleic acid in a 2:1 to 4:1 mole ratio.
• the amount of units derived from electrically conductive monomers (a') serves to balance the requirements for antistatic protection with sufficient capability of the copolymer to become crosslinked through the carboxylic groups of units derived from monomers (b').
• monomer (a') may be styrene sulfonic acid, vinyltoluene sulfonic acid, ⁇ -methyl-styrene sulfonic acid, 2-ethyl-styrene sulfonic acid, 3-acryloyloxypropane-1-sulfonic acid, 3-methacryloyloxypropane-1-sulfonic acid, 2-acrylamido-2-methylpropane-sulfonic acid, 3-methacryloyloxypropane-1-methyl-1-sulfonic acid, acryloylmethane-sulfonic acid, 4-acryloyloxybutane-1-sulfonic acid, 4-acryloyloxybutane-1-sulfonic acid, 2-acryloyloxyethane-1-sulfonic acid, 2-acrylamidopropane-1-sulfonic acid, 2-methacrylamido-2-methylpropane-1-sulfonic acid, 3-methacryl
• Monomer (b') may be maleic acid, acrylic acid, methacrylic acid, 2-butenoic acid.
• Monomer (c'), if present, is to be chosen so as not to negatively affect the electrical conductivity, water solubility and crosslinking capability of the polymers according to the present invention.
• Examples of monomers (c') are ethylenic monomers (such as isoprene, 1,3-butadiene, vinyl chloride, ethylene, propylene), styrene type monomers (such as styrene, vinyltoluene, ⁇ -methylstyrene, 2-ethyl-styrene, 1-vinylnaphthalene), 2-alkenoic acid esters (such methyl, ethyl, propyl, butyl, hexyl esters of acrylic, methacrylic, ⁇ -ethylacrylic, ⁇ -propylacrylic, 2-butenoic acids), acrylamide monomers (such as acrylamide, N-methylacrylamide, N,N-dimethylacrylamide, N-butylacrylamide, N-chloromethylacrylamide) and vinyl acetate.
• ethylenic monomers such as isoprene, 1,3-butadiene, vinyl chloride, ethylene
• the component (b) of the antistatic layer of the present invention is a polyfunctional epoxide crosslinking agent, that is an organic compound, including a polymeric compound, containing at least two epoxide groups therein.
• component (b) are as follows: bis(2,3-epoxypropyl) ether, vinyl cyclohexene dioxide, ethylene bisglycidyl ether, bis(2,3-epoxypropylethyl) ether, hydroquinone bisglycidyl ether, resorcinol bisglycidyl ether, diepoxybutane, diepoxyhexane, bisglycidyl thioether, glycerol trisglycidyl ether, bisglycidyl malonic acid diethyl ester, bisglycidyl sulfone, N,N-bisglycidyl piperazine, trisglycidyl phosphate, 2,4,6-trisglycidyl
• component (1) of the antistatic layer of the present invention can be found in EP 589,329 and EP 486,982.
• the component (2) of the antistatic layer of the present invention is a non-ionic perfluoroalkyl(ene)polyoxyalkylene surfactant.
• the component (2) of the antistatic layer of the present invention is a non-ionic perfluoroalkyl(ene)polyoxyethylene surfactant.
• non-ionic perfluoroalkyl(ene)polyoxyalkylene surfactant means a non-ionic surfactant comprising a compound or a mixture of compounds having at least one alkyl or alkylene group of from 3 to 16 carbon atoms wherein the hydrogens are totally replaced by fluorine atoms joined directly or through a linking group to a polyoxyalkylene group comprising from 6 to 24 oxyalkylene groups.
• non-ionic perfluoroalkyl(ene)polyoxyethylene surfactant means a non-ionic surfactant comprising a compound or a mixture of compounds having at least one alkyl or alkylene group of from 3 to 16 carbon atoms wherein the hydrogens are totally replaced by fluorine atoms joined directly or through a linking group to a polyoxyethylene group comprising from 6 to 24 oxyethylene groups.
• the preferred non-ionic perfluoroalkyl(ene)polyoxyethylene surfactants can be represented by the following formula: wherein R and R' are, independently, hydrogen or a lower alkyl of from 1 to 4 carbon atoms, Z is a divalent linking group, m is 0 or 1, n is an integer from 3 to 16, x is (n+1) or (n-1), and y is a number from 6 to 24.
• Z can be any of -O-, -S-, -(CH 2 )p-, wherein p is an integer from 1 to 6, -NR 1 -, -SO-, -SO 2 -, NR 1 - SO 2 -, -SO 2 NR 1 -, -CO-, -COO-, -CONR 1 -, NR 1 CO-, -NR 1 CONR 2 -, -NR 1 SO 2 NR 2 -, wherein R 1 and R 2 , indipendently, can be hydrogen, an alkyl group, and an aryl group.
• the described chemical material includes the basic group and that group with conventional substitution.
• moiety is used to describe a chemical compound or substituent only an unsubstituted chemical material is intended to be included.
• the aqueous coating composition can comprise from 1 to 100 g/l, preferably from 5 to 50 g/l of antistatic polymer (a), from 0.1 to 10 g/l, preferably from 0.5 to 5 g/l of crosslinking agent (b), and from 0.01 to 5 g/l, preferably from 0.1 to 1 g/l of non-ionic perfluoroalkyl(ene)polyoxyalkylene surfactant.
• the resulting aqueous coating composition may be coated onto any suitable polymeric photographic base, but the preferred base is polyethyleneterephthalate film which has been subbed with a layer of resin, or layers of resin and gelatin.
• the antistatic coating is usually provided in coating weight based on the dry weight of from 0.01 g/m 2 to 1 g/m 2 .
• the non-ionic perfluoroalkyl(ene)polyoxyalkylene surfactant coating weight of the dry antistatic coating ranges from about 0.001 to 0.5 g/m 2 . Lower coating weights usually provide less adequate antistatic protection and higher coating weights usually give less transparent layers.
• the coating may be performed by conventional coating techniques, such as, for example, air knife coating, gravure coating, doctor roller coating.
• the antistatic layer of the present invention may also contain other addenda, such as, for example, matting agents, plasticizers, lubricants, surfactants, dyes, and haze reducing agents.
• addenda such as, for example, matting agents, plasticizers, lubricants, surfactants, dyes, and haze reducing agents.
• binders is not required, but limited amounts (such as, for example, less than 20%, preferably less than 10% in weight based on the weight of component (a)), of binders, such as gelatin, may be added to the coating composition to improve coating quality of the antistatic layer.
• the reaction of (a) and (b) is usually effected during coating and drying of components (a) and (b) onto the polymeric substrate. Heating may be used to accelerate drying and/or the reaction of the components (curing) to form a permanent antistatic layer. Air temperatures of from 20 to 200°C are useful for the drying-curing step, while the preferred range is 50 to 160°C. Catalysts may also be used to speed up the reaction.
• the reaction product of (a) and (b) is a crosslinked product, having three-dimensional bonding within the layer.
• the crosslinking helps provide a permanent antistatic layer which is water-resistant and keeps low molecular weight materials within the component (a) from migrating out of the antistatic layer. Migration is reduced or eliminated into other photographic layers and/or into aqueous processing solutions by the tightening effect of the crosslinking on the internal structure of the antistatic layer.
• non-ionic perfluoroalkyl(ene)polyoxyalkylene surfactant(s) provides a good coating quality and avoids the formation of the so-called repellency spot in correspondence of dirt, oil or other contaminants which can be present on the polymeric base.
• the imaging elements useful in the present invention may be any of the well-known elements for imaging in the field of graphic arts, printing, medical and information systems.
• Silver halide, photopolymers, diazo, vesicular image-forming systems may be used, silver halide being preferred.
• Typical imaging element constructions of the present invention comprise:
• silver halide photographic elements include black-and-white and color photographic elements.
• the silver halide employed in this invention may be any of silver chloride, silver bromide, silver iodide, silver chlorobromide, silver chloroiodide, silver bromoiodide, silver chloroiodobromide, and the like.
• the silver halide grains in the photographic emulsion may be regular grains having a regular crystal structure such as cube, octahedron, and tetradecahedron, or the spherical or irregular crystal structure, or those having crystal defects such as twin planes, or those having a tabular form, or combinations thereof.
• gelatin is advantageously used, but other hydrophilic colloids may be used such as gelatin substitutes, collodion, gum arabic, cellulose ester derivatives such as alkyl esters of carboxylated cellulose, hydroxy ethyl cellulose, carboxy methyl cellulose, synthetic resins, such as the amphoteric copolymers described in US Pat. No. 2,949,442, polyvinyl alcohol, and others well known in the art.
• the photographic elements utilizing the antistatic layer of this invention have radiation-sensitive silver halide emulsion layers, i.e. silver halide emulsions sensitive to the visible, ultraviolet or infrared light.
• the silver halide emulsions may be optically sensitized by any of the spectral sensitizers commonly used to produce the desired sensitometric characteristics.
• the following examples also report three adhesion values: the first is the dry adhesion value and refers to the adhesion of the silver halide emulsion layers and of the auxiliary gelatin layers to the antistatic base prior to the photographic processing; the second value is the wet adhesion value and refers to the adhesion of the above layers to the antistatic base during the photographic processing (developer and fixer); the third adhesion value is the dry adhesion value and refers to the adhesion of the above layers to the antistatic base after photographic processing.
• the dry adhesion was measured by tearing samples of the film, applying a 3M ScotchTM 5959 Pressure Sensitive Tape along the tear line of the film and separating rapidly the tape from the film: the layer adhesion was evaluated according to a scholastic method giving a value of 0 when the whole layer was removed from the base, and a value of 10 when no part thereof was removed from the base, and intermediate values for intermediate situations.
• the wet adhesion was measured by drawing some lines with a pencil point to form an asterisk on the film just taken out from the processing bath and by rubbing on the lines with a finger.
• the adhesion of the layers was evaluated according to a scholastic method by giving a value of 0 when the layers were totally removed from the base, a value of 10 when no portion thereof was removed, and intermediate values for intermediate cases.
• subbing compositions were prepared and coated onto a poly(ethylene terephthalate) film base (PET) resin-subbed on both sides with the terpolymer (vinylidene chloride-itaconic acid-ethylmethacrylate) by the gravure roller coating technique.
• the amounts of the components reported in the following Table 1 are expressed in grams. All the subbing compositions were coated at a wet coverage of 10 ml/m 2 and coating speed of 60 m/min.
• the coating quality was evaluated by scholastic rating from 0 to 10, wherein the higher the score, the better the quality.
• Table 2 reports the values of surface electrical resistivity and coating quality for the various samples.
• subbings of example 1 were overcoated with a conventional gelatin antihalation layer containing antihalation dyes, a surfactant and a hardener and with a protective layer containing a matting agent, a surfactant and a hardener (Coatings 7,8,9,10,11,12, respectively).
• the two layers were coated at approximately pH 6.
• the total gelatin coverage is about 4.5 g/m 2 and the thickness is approximately 4.5 micrometers.
• a conventional black-and-white silver halide photographic emulsion was coated on the opposite side of each coating. The characteristics of the coatings are reported in the following Table 3. Adhesion values are expressed by scholastic rating (0-10) in which the higher the number, the better the adhesion. Table 3 Coating samples 7 Comp.

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Citations (5)

• 1995
  • 1995-05-24 EP EP95107935A patent/EP0745896A1/de not_active Withdrawn
• 1996
  • 1996-05-22 JP JP8126972A patent/JPH08319361A/ja active Pending

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