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EP0828184A1 - Elément formateur d'image contenant un mélange électroconducteur polymérique - Google Patents

Elément formateur d'image contenant un mélange électroconducteur polymérique Download PDF

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Publication number
EP0828184A1
EP0828184A1 EP97202603A EP97202603A EP0828184A1 EP 0828184 A1 EP0828184 A1 EP 0828184A1 EP 97202603 A EP97202603 A EP 97202603A EP 97202603 A EP97202603 A EP 97202603A EP 0828184 A1 EP0828184 A1 EP 0828184A1
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EP
European Patent Office
Prior art keywords
film
layer
imaging element
conductive
sulfonic acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP97202603A
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German (de)
English (en)
Inventor
Nicholas Eastman Kodak Compay Zumbulyadis
Lori Jeanne Eastman Kodak Company Shaw-Klein
Sylvia Alice Eastman Kodak Company Gardner
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Eastman Kodak Co
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Eastman Kodak Co
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Filing date
Publication date
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Publication of EP0828184A1 publication Critical patent/EP0828184A1/fr
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Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/10—Bases for charge-receiving or other layers
    • G03G5/105—Bases for charge-receiving or other layers comprising electroconductive macromolecular compounds
    • G03G5/108—Bases for charge-receiving or other layers comprising electroconductive macromolecular compounds the electroconductive macromolecular compounds being anionic
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
    • B41M5/42—Intermediate, backcoat, or covering layers
    • B41M5/44—Intermediate, backcoat, or covering layers characterised by the macromolecular compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
    • B41M5/52—Macromolecular coatings
    • B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
    • 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

Definitions

  • the present invention relates in general to imaging elements, such as photographic, electrostatographic, inkjet and thermal imaging elements, and in particular to imaging elements comprising a support, an image-forming layer and a transparent electrically-conductive layer. More specifically, this invention relates to the preparation of water-soluble blends of polyaniline complexes of poly(styrene sulfonic acid) or poly(styrene-co-styrene sulfonic acid) with other polymers that can form conductive films that are sufficiently transparent for photographic applications, and retain their conductivity after photographic processing with or without the use of a protective overcoat layer.
  • the charge generated during the coating process results primarily from the tendency of webs of high dielectric polymeric film base to charge during winding and unwinding operations (unwinding static), during transport through the coating machines (transport static), and during post-coating operations such as slitting and spooling. Static charge can also be generated during the use of the finished photographic film product.
  • unwinding static winding and unwinding operations
  • transport static transport through the coating machines
  • post-coating operations such as slitting and spooling.
  • Static charge can also be generated during the use of the finished photographic film product.
  • the winding of roll film out of and back into the film cassette especially in a low relative humidity environment, can result in static charging.
  • high-speed automated film processing can result in static charge generation.
  • Sheet films are especially subject to static charging during removal from light-tight packaging (e.g., x-ray films).
  • Antistatic layers can be applied to one or to both sides of the film base as subbing layers either beneath or on the side opposite to the light-sensitive silver halide emulsion layers.
  • An antistatic layer can alternatively be applied as an outer coated layer either over the emulsion layers or on the side of the film base opposite to the emulsion layers or both.
  • the antistatic agent can be incorporated into the emulsion layers.
  • the antistatic agent can be directly incorporated into the film base itself.
  • a wide variety of electrically-conductive materials can be incorporated into antistatic layers to produce a wide range of conductivities.
  • Most of the traditional antistatic systems for photographic applications employ ionic conductors. Charge is transferred in ionic conductors by the bulk diffusion of charged species through an electrolyte.
  • Antistatic layers containing simple inorganic salts, alkali metal salts of surfactants, ionic conductive polymers, polymeric electrolytes containing alkali metal salts, and colloidal metal oxide sols (stabilized by metal salts) have been described previously.
  • the conductivities of these ionic conductors are typically strongly dependent on the temperature and relative humidity in their environment. At low humidities and temperatures, the diffusional mobilities of the ions are greatly reduced and conductivity is substantially decreased.
  • antistatic backcoatings often absorb water, swell, and soften. In roll film, this results in adhesion of the backcoating to the emulsion side of the film. Also, many of the inorganic salts, polymeric electrolytes, and low molecular weight surfactants used are water-soluble and are leached out of the antistatic layers during processing, resulting in a loss of antistatic function.
  • colloidal metal oxide sols which exhibit ionic or electronic conductivity when included in antistatic layers are often used in imaging elements. Typically, alkali metal salts or anionic surfactants are used to stabilize these sols.
  • a thin antistatic layer consisting of a gelled network of colloidal metal oxide particles (e.g., silica, antimony pentoxide, alumina, titania, stannic oxide, zirconia) with an optional polymeric binder to improve adhesion to both the support and overlying emulsion layers has been disclosed in EP 250,154.
  • An optional ambifunctional silane or titanate coupling agent can be added to the gelled network to improve adhesion to overlying emulsion layers (e.g., EP 301,827; U.S.
  • Patent No. 5,204,219) along with an optional alkali metal orthosilicate to minimize loss of conductivity by the gelled network when it is overcoated with gelatin-containing layers
  • an optional alkali metal orthosilicate to minimize loss of conductivity by the gelled network when it is overcoated with gelatin-containing layers
  • coatings containing colloidal metal oxides e.g., antimony pentoxide, alumina, tin oxide, indium oxide
  • colloidal silica with an organopolysiloxane binder afford enhanced abrasion resistance as well as provide antistatic function (U.S. Patent Nos. 4,442,168 and 4,571,365).
  • Antistatic systems employing electronic conductors have also been described. Because the conductivity depends predominantly on electronic mobilities rather than ionic mobilities, the observed electronic conductivity is independent of relative humidity and only slightly influenced by the ambient temperature. Antistatic layers have been described which contain conjugated polymers, conductive carbon particles or semiconductive inorganic particles.
  • Trevoy U.S. Patent 3,245,833 has taught the preparation of conductive coatings containing semiconductive silver or copper iodide dispersed as particles less than 0.1 ⁇ m in size in an insulating film-forming binder, exhibiting a surface resistivity of 10 2 to 10 11 ohms per scare .
  • the conductivity of these coatings is substantially independent of the relative humidity.
  • the coatings are relatively clear and sufficiently transparent to permit their use as antistatic coatings for photographic film.
  • Trevoy found (U.S. Patent 3,245,833)
  • Patent 3,428,451 that it was necessary to overcoat the conductive layer with a dielectric, water-impermeable barrier layer to prevent migration of semiconductive salt into the silver halide emulsion layer during processing. Without the barrier layer, the semiconductive salt could interact deleteriously with the silver halide layer to form fog and a loss of emulsion sensitivity. Also, without a barrier layer, the semiconductive salts are solubilized by processing solutions, resulting in a loss of antistatic function.
  • a highly effective antistatic layer incorporating an "amorphous" semiconductive metal oxide has been disclosed by Guestaux (U.S. Patent 4,203,769).
  • the antistatic layer is prepared by coating an aqueous solution containing a colloidal gel of vanadium pentoxide onto a film base.
  • the colloidal vanadium pentoxide gel typically consists of entangled, high aspect ratio, flat ribbons 50-100 ⁇ wide, 10 ⁇ thick, and 1,000-10,000 ⁇ long. These ribbons stack flat in the direction perpendicular to the surface when the gel is coated onto the film base.
  • vanadium pentoxide gels (1 ⁇ -1 cm -1 ) which are typically three orders of magnitude greater than is observed for similar thickness films containing crystalline vanadium pentoxide particles.
  • low surface resistivities can be obtained with very low vanadium pentoxide coverages. This results in low optical absorption and scattering losses.
  • the thin films are highly adherent to appropriately prepared film bases.
  • vanadium pentoxide is soluble at high pH and must be overcoated with a non-permeable, hydrophobic barrier layer in order to survive processing. When used with a conductive subbing layer, the barrier layer must be coated with a hydrophilic layer to promote adhesion to emulsion layers above. (See Anderson et al, U.S. Patent 5,006,451.)
  • Conductive fine particles of crystalline metal oxides dispersed with a polymeric binder have been used to prepare optically transparent, humidity insensitive, antistatic layers for various imaging applications.
  • Many different metal oxides -- such as ZnO, TiO 2 , ZrO 2 , SnO 2 , Al 2 O 3 , In 2 O 3 , SiO 2 , MgO, BaO, MoO 3 and V 2 O 5 -- are alleged to be useful as antistatic agents in photographic elements or as conductive agents in electrostatographic elements in such patents as U.S. 4,275,103, 4,394,441, 4,416,963, 4,418,141, 4,431,764, 4,495,276, 4,571,361, 4,999,276 and 5,122,445.
  • Preferred metal oxides are antimony doped tin oxide, aluminum doped zinc oxide, and niobium doped titanium oxide. Surface resistivities are reported to range from 10 6 -10 9 ohms per square for antistatic layers containing the preferred metal oxides. In order to obtain high electrical conductivity, a relatively large amount (0.1-10 g/m 2 ) of metal oxide must be included in the antistatic layer. This results in decreased optical transparency for thick antistatic coatings.
  • the high values of refractive index (>2.0) of the preferred metal oxides necessitates that the metal oxides be dispersed in the form of ultrafine ( ⁇ 0.1 ⁇ m) particles in order to minimize light scattering (haze) by the antistatic layer.
  • Antistatic layers comprising electro-conductive ceramic particles, such as particles of TiN, NbB 2 , TiC, LaB 6 or MoB, dispersed in a binder such as a water-soluble polymer or solvent-soluble resin are described in Japanese Kokai No. 4/55492, published February 24, 1992.
  • Fibrous conductive powders comprising antimony-doped tin oxide coated onto non-conductive potassium titanate whiskers have been used to prepare conductive layers for photographic and electrographic applications. Such materials are disclosed, for example, in U.S. Patents, 4,845,369 and 5,116,666. Layers containing these conductive whiskers dispersed in a binder reportedly provide improved conductivity at lower volumetric concentrations than other conductive fine particles as a result of their higher aspect ratio.
  • the benefits obtained as a result of the reduced volume percentage requirements are offset by the fact that these materials are relatively large in size such as 10 to 20 micrometers in length, and such large size results in increased light scattering and hazy coatings.
  • Electrically-conductive layers are also commonly used in imaging elements for purposes other than providing static protection.
  • imaging elements comprising a support, an electrically-conductive layer that serves as an electrode, and a photoconductive layer that serves as the image-forming layer.
  • Electrically-conductive agents utilized as antistatic agents in photographic silver halide imaging elements are often also useful in the electrode layer of electrostatographic imaging elements.
  • an imaging element for use in an imaging-forming process comprises a support, an image-forming layer, and a tranparent electrically-conductive layer comprising polyaniline styrene sulfonic acid.
  • the transparent electrically-conductive layer includes the polyaniline styrene sulfonic acid dispersed in a film-forming binder.
  • the imaging elements of this invention can be of many different types depending on the particular use for which they are intended. Such elements include, for example, photographic, electrostatographic, photothermographic, migration, electrothermographic, dielectric recording and thermal-dye-transfer imaging elements.
  • Photographic elements which can be provided with an antistatic layer in accordance with this invention can differ widely in structure and composition.
  • they can vary greatly in regard to the type of support, the number and composition of the image-forming layers, and the kinds of auxiliary layers that are included in the elements.
  • the photographic elements can be still films, motion picture films, x-ray films, graphic arts films, paper prints or microfiche. They can be black-and-white elements, color elements adapted for use in a negative-positive process, or color elements adapted for use in a reversal process.
  • Photographic elements can comprise any of a wide variety of supports.
  • Typical supports include cellulose nitrate film, cellulose acetate film, poly(vinyl acetal) film, polystyrene film, poly(ethylene terephthalate) film, poly(ethylene naphthalate) film, polycarbonate film, glass, metal, paper, polymer-coated paper, and the like.
  • the image-forming layer or layers of the element typically comprise a radiation-sensitive agent, e.g., silver halide, dispersed in a hydrophilic water-permeable colloid.
  • Suitable hydrophilic vehicles include both naturally-occurring substances such as proteins, for example, gelatin, gelatin derivatives, cellulose derivatives, polysaccharides such as dextran, gum arabic, and the like, and synthetic polymeric substances such as water-soluble polyvinyl compounds like poly(vinylpyrrolidone), acrylamide polymers, and the like.
  • a particularly common example of an image-forming layer is a gelatin-silver halide emulsion layer.
  • an image comprising a pattern of electrostatic potential is formed on an insulative surface by any of various methods.
  • the electrostatic latent image may be formed electrophotographically (i.e., by imagewise radiation-induced discharge of a uniform potential previously formed on a surface of an electrophotographic element comprising at least a photoconductive layer and an electrically-conductive substrate), or it may be formed by dielectric recording (i.e., by direct electrical formation of a pattern of electrostatic potential on a surface of a dielectric material).
  • the electrostatic latent image is then developed into a toner image by contacting the latent image with an electrographic developer (if desired, the latent image can be transferred to another surface before development).
  • the resultant toner image can then be fixed in place on the surface by application of heat and/or pressure or other known methods (depending upon the nature of the surface and of the toner image) or can be transferred by known means to another surface, to which it then can be similarly fixed.
  • the surface to which the toner image is intended to be ultimately transferred and fixed is the surface of a sheet of plain paper or, when it is desired to view the image by transmitted light (e.g., by projection in an overhead projector), the surface of a transparent film sheet element.
  • the electrically-conductive layer can be a separate layer, a part of the support layer or the support layer.
  • conducting layers There are many types of conducting layers known to the electrostatographic art, the most common being listed below:
  • Conductive layers (d), (e) and (f) can be transparent and can be employed where transparent elements are required, such as in processes where the element is to be exposed from the back rather than the front or where the element is to be used as a transparency.
  • Thermally processable imaging elements including films and papers, for producing images by thermal processes are well known. These elements include thermographic elements in which an image is formed by imagewise heating the element. Such elements are described in, for example, Research Disclosure , June 1978, Item No. 17029; U.S. Patent No. 3,457,075; U.S. Patent No. 3,933,508; and U.S. Patent No. 3,080,254.
  • Photothermographic elements typically comprise an oxidation-reduction image-forming combination which contains an organic silver salt oxidizing agent, preferably a silver salt of a long-chain fatty acid.
  • organic silver salt oxidizing agents are resistant to darkening upon illumination.
  • Preferred organic silver salt oxidizing agents are silver salts of long-chain fatty acids containing 10 to 30 carbon atoms.
  • useful organic silver salt oxidizing agents are silver behenate, silver stearate, silver oleate, silver laurate, silver hydroxystearate, silver caprate, silver myristate and silver palmitate. Combinations of organic silver salt oxidizing agents are also useful.
  • useful silver salt oxidizing agents which are not silver salts of long-chain fatty acids include, for example, silver benzoate and silver benzotriazole.
  • Photothermographic elements also comprise a photosensitive component which consists essentially of photographic silver halide.
  • a photosensitive component which consists essentially of photographic silver halide.
  • the latent image silver from the silver halide acts as a catalyst for the oxidation-reduction image-forming combination upon processing.
  • a preferred concentration of photographic silver halide is within the range of 0.01 to 10 moles of photographic silver halide per mole of organic silver salt oxidizing agent, such as per mole of silver behenate, in the photothermographic material.
  • Other photosensitive silver salts are useful in combination with the photographic silver halide if desired.
  • Preferred photographic silver halides are silver chloride, silver bromide, silver bromoiodide, silver chlorobromoiodide and mixtures of these silver halides. Very fine grain photographic silver halide is especially useful.
  • Migration imaging processes typically involve the arrangement of particles on a softenable medium.
  • the medium which is solid and impermeable at room temperature, is softened with heat or solvents to permit particle migration in an imagewise pattern.
  • migration imaging can be used to form a xeroprinting master element.
  • a monolayer of photosensitive particles is placed on the surface of a layer of polymeric material which is in contact with a conductive layer.
  • the element is subjected to imagewise exposure which softens the polymeric material and causes migration of particles where such softening occurs (i.e., image areas).
  • image areas can be charged, developed, and transferred to paper.
  • Another type of migration imaging technique utilizes a solid migration imaging element having a substrate and a layer of softenable material with a layer of photosensitive marking material deposited at or near the surface of the softenable layer.
  • a latent image is formed by electrically charging the member and then exposing the element to an imagewise pattern of light to discharge selected portions of the marking material layer.
  • the entire softenable layer is then made permeable by application of the marking material, heat or a solvent, or both.
  • the portions of the marking material which retain a differential residual charge due to light exposure will then migrate into the softened layer by electrostatic force.
  • An imagewise pattern may also be formed with colorant particles in a solid imaging element by establishing a density differential (e.g., by particle agglomeration or coalescing) between image and non-image areas.
  • colorant particles are uniformly dispersed and then selectively migrated so that they are dispersed to varying extents without changing the overall quantity of particles on the element.
  • Another migration imaging technique involves heat development, as described by R. M. Schaffert, Electrophotography , (Second Edition, Focal Press, 1980), pp. 44-47 and U.S. Patent 3,254,997.
  • an electrostatic image is transferred to a solid imaging element, having colloidal pigment particles dispersed in a heat-softenable resin film on a transparent conductive substrate. After softening the film with heat, the charged colloidal particles migrate to the oppositely charged image. As a result, image areas have an increased particle density, while the background areas are less dense.
  • laser toner fusion which is a dry electrothermographic process
  • uniform dry powder toner depositions on non-photosensitive films, papers, or lithographic printing plates are imagewise exposed with high power (0.2-0.5 W) laser diodes thereby, "tacking" the toner particles to the substrate(s).
  • the toner layer is made, and the non-imaged toner is removed, using such techniques as electrographic "magnetic brush” technology similar to that found in copiers.
  • a final blanket fusing step may also be needed, depending on the exposure levels.
  • imaging elements which employ an antistatic layer are dye-receiving elements used in thermal dye transfer systems.
  • Thermal dye transfer systems are commonly used to obtain prints from pictures which have been generated electronically from a color video camera. According to one way of obtaining such prints, an electronic picture is first subjected to color separation by color filters. The respective color-separated images are then converted into electrical signals. These signals are then operated on to produce cyan, magenta and yellow electrical signals. These signals are then transmitted to a thermal printer. To obtain the print, a cyan, magenta or yellow dye-donor element is placed face-to-face with a dye-receiving element. The two are then inserted between a thermal printing head and a platen roller. A line-type thermal printing head is used to apply heat from the back of the dye-donor sheet.
  • the thermal printing head has many heating elements and is heated up sequentially in response to the cyan, magenta and yellow signals. The process is then repeated for the other two colors. A color hard copy is thus obtained which corresponds to the original picture viewed on a screen. Further details of this process and an apparatus for carrying it out are described in U.S. Patent No. 4,621,271.
  • Another type of image-forming process in which the imaging element can make use of an electrically-conductive layer is a process employing an imagewise exposure to electric current of a dye-forming electrically-activatable recording element to thereby form a developable image followed by formation of a dye image, typically by means of thermal development.
  • Dye-forming electrically activatable recording elements and processes are well known and are described in such patents as U.S. 4,343,880 and 4,727,008.
  • the image-forming layer can be any of the types of image-forming layers described above, as well as any other image-forming layer known for use in an imaging element.
  • the imaging elements of the present invention at least one electrically-conductive which comprises polyaniline styrene sulfonic acid in effective amount to provide antistatic properties to the electrically-conductive layer.
  • Binders useful in antistatic layers containing polyaniline styrene sulfonic acid include: water-soluble polymers such as gelatin, gelatin derivatives, maleic acid anhydride copolymers; cellulose compounds such as carboxymethyl cellulose, hydroxyethyl cellulose, cellulose acetate butyrate, diacetyl cellulose or triacetyl cellulose; synthetic hydrophilic polymers such as polyvinyl alcohol, poly-N-vinylpyrrolidone, acrylic acid copolymers, polyacrylamides, their derivatives and partially hydrolyzed products, vinyl polymers and copolymers such as polyvinyl acetate and polyacrylate acid esters; derivatives of the above polymers; and other synthetic resins.
  • water-soluble polymers such as gelatin, gelatin derivatives, maleic acid anhydride copolymers
  • cellulose compounds such as carboxymethyl cellulose, hydroxyethyl cellulose, cellulose acetate butyrate, diacetyl cellulose or tri
  • Suitable binders include aqueous emulsions of addition-type polymers and interpolymers prepared from ethylenically unsaturated monomers such as acrylates including acrylic acid, methacrylates including methacrylic acid, acrylamides and methacrylamides, itaconic acid and its half-esters and diesters, styrenes including substituted styrenes, acrylonitrile and methacrylonitrile, vinyl acetates, vinyl ethers, vinyl and vinylidene halides, olefins, and aqueous dispersions of polyurethanes or polyesterionomers.
  • acrylates including acrylic acid, methacrylates including methacrylic acid, acrylamides and methacrylamides, itaconic acid and its half-esters and diesters
  • styrenes including substituted styrenes
  • acrylonitrile and methacrylonitrile vinyl acetates
  • vinyl ethers vinyl
  • the preparation of the poly(aniline/polystyrene sulfonic acid) were made in situ by oxidative polymerization of aniline in aqueous solution in the presence of poly(styrene sulfonic acid) using ammonium peroxodisulfate as the oxidant.
  • the conductive coatings were immersed in room-temperature baths of developer (C-41 developer, Eastman Kodak) for 15 seconds. They were then rinsed for 5 seconds in deionized water and left to dry at room temperature. The samples were visually inspected for evidence of hue shift, and the surface resistivity was again measured.
  • developer C-41 developer, Eastman Kodak
  • the table below includes information concerning the total dry coverage of the conductive film, and the portion (weight %) of the film comprising the polyaniline-styrene sulfonic acid of this invention.
  • the examples demonstrate the wide range of polymeric and non-polymeric binders which may be successfully used in combination with polyaniline-styrene-sulfonic acid. In addition, they demonstrate the potential usefulness of various classes of crosslinkers in combination with such binders for improved chemical resistance.
  • coatings such as those described here may be overcoated with materials known in the art; for example, polyalkylacrylates, methacrylates or the like, polyurethanes, cellulose esters, styrene-containing polymers, etc. Such an overcoat may be preferred in the harsher conditions (high temperature and long times) of an actual photographic processing event.
  • the use of polyaniline styrene sulfonic acid in an electrically-conductive layer layer in imaging elements overcomes many of the difficulties that have heretofore been encountered in the prior art.
  • the use of the polyaniline styrene sulfonic acid provides a transparent electrically-conductive layer which is process surviving and can be manufactured at a reasonable cost.
  • the aniline may be a substituted aniline.
  • the electrically-conductive layer is resistant to the effects of humidity change that is durable and abrasion resistant, thereby eliminating the need of an overcoat layer on a photographic imaging element.

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  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Optics & Photonics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
EP97202603A 1996-09-04 1997-08-23 Elément formateur d'image contenant un mélange électroconducteur polymérique Withdrawn EP0828184A1 (fr)

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US707570 1996-09-04

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2352512A (en) * 1999-07-23 2001-01-31 Toshiba Res Europ Ltd A radiation probe and dectecting tooth decay
WO2002065484A1 (fr) * 2001-02-09 2002-08-22 E. I. Du Pont De Nemours And Company Dispersions conductrices aqueuses de polyaniline presentant une viscosite augmentee

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Publication number Priority date Publication date Assignee Title
US3856530A (en) * 1969-10-29 1974-12-24 Agfa Gevaert Photographic polyester film material comprising antistatic layer
JPH0521824A (ja) * 1991-07-12 1993-01-29 Mitsubishi Paper Mills Ltd 光電変換素子
JPH0632845A (ja) * 1992-07-20 1994-02-08 Showa Denko Kk 導電性高分子複合物の製造方法
JPH08211555A (ja) * 1995-02-02 1996-08-20 Konica Corp 帯電防止層を有するハロゲン化銀写真感光材料
EP0758671A2 (fr) * 1995-08-10 1997-02-19 Eastman Kodak Company Composition électroconductrice et élements contenant de complexe de polyaniline solubilisé

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3856530A (en) * 1969-10-29 1974-12-24 Agfa Gevaert Photographic polyester film material comprising antistatic layer
JPH0521824A (ja) * 1991-07-12 1993-01-29 Mitsubishi Paper Mills Ltd 光電変換素子
JPH0632845A (ja) * 1992-07-20 1994-02-08 Showa Denko Kk 導電性高分子複合物の製造方法
JPH08211555A (ja) * 1995-02-02 1996-08-20 Konica Corp 帯電防止層を有するハロゲン化銀写真感光材料
EP0758671A2 (fr) * 1995-08-10 1997-02-19 Eastman Kodak Company Composition électroconductrice et élements contenant de complexe de polyaniline solubilisé

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Title
DATABASE WPI Section Ch Week 9309, Derwent World Patents Index; Class A85, AN 93-072727, XP002049682 *
DATABASE WPI Section Ch Week 9410, Derwent World Patents Index; Class A26, AN 94-080017, XP002049684 *
DATABASE WPI Section Ch Week 9643, Derwent World Patents Index; Class A23, AN 96-429023, XP002049683 *
DEFIEUW G ET AL: "THERMAL DYE SUBLIMATION TRANSFER", RESEARCH DISCLOSURE, no. 334, 1 February 1992 (1992-02-01), pages 155 - 159, XP000291266 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2352512A (en) * 1999-07-23 2001-01-31 Toshiba Res Europ Ltd A radiation probe and dectecting tooth decay
GB2352512B (en) * 1999-07-23 2002-03-13 Toshiba Res Europ Ltd A radiation probe and detecting tooth decay
US8027709B2 (en) 1999-07-23 2011-09-27 Teraview Limited Radiation probe and detecting tooth decay
WO2002065484A1 (fr) * 2001-02-09 2002-08-22 E. I. Du Pont De Nemours And Company Dispersions conductrices aqueuses de polyaniline presentant une viscosite augmentee

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