EP0035614B2 - Films photographiques avec une couche adhésive et procédés pour leur fabrication - Google Patents

Films photographiques avec une couche adhésive et procédés pour leur fabrication Download PDF

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Publication number
EP0035614B2
EP0035614B2 EP19800300759 EP80300759A EP0035614B2 EP 0035614 B2 EP0035614 B2 EP 0035614B2 EP 19800300759 EP19800300759 EP 19800300759 EP 80300759 A EP80300759 A EP 80300759A EP 0035614 B2 EP0035614 B2 EP 0035614B2
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EP
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Prior art keywords
mole
acid
subbing
comonomer
copolymer
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Expired
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EP19800300759
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German (de)
English (en)
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EP0035614A1 (fr
EP0035614B1 (fr
Inventor
Cyril John Ealding
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Imperial Chemical Industries Ltd
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Imperial Chemical Industries Ltd
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Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to EP19800300759 priority Critical patent/EP0035614B2/fr
Priority to DE8080300759T priority patent/DE3067999D1/de
Publication of EP0035614A1 publication Critical patent/EP0035614A1/fr
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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
    • G03C1/91—Photosensitive materials characterised by the base or auxiliary layers characterised by subbing layers or subbing means
    • G03C1/93—Macromolecular substances therefor

Definitions

  • the present invention relates to a light-sensitive photographic material comprising a light-sensitive photographic emulsion applied to a coated film base and to processes for the production of the light-sensitive photographic material.
  • the present invention provides a subbing layer copolymer which is effective in promoting the adhesion of a light-sensitive photographic emulsion to a film support of a synthetic linear polyester.
  • a photographic material comprises (1) a self-supporting film of a synthetic linear polyester, (2) a continuous subbing layer applied to at least one surface of said self-supporting film and (3) a light-sensitive photographic emulsion layer applied directly or indirectly to the subbing layer, which subbing layer comprises a water-insoluble copolymer comprising (a) a comonomer selected from acrylic acid, methacrylic acid or a derivative of acrylic acid or methacrylic acid characterised in that the subbing layer copolymer further comprises (b) a copolymerisable sulphonated ethylenically unsaturated comonomer selected from vinyl sulphonic acid, allyl sulphonic acid, methallyl sulphonic acid, p-styrene sulphonic acid and the salts of these acids, said comonomers (a) and (b) being present in the respective molar percentages in the ranges (a) 26 to 99% and (b) 1 to 50%.
  • the invention also provides a process for the production of a light-sensitive photographic material which comprises applying a continuous subbing layer to at least one surface of a self-supporting film of a synthetic linear polyester and applying a light-sensitive photographic emulsion layer directly or indirectly over the subbing layer, wherein the subbing layer is applied from a film-forming composition comprising a water-insoluble copolymer which comprises (a) a comonomer selected from acrylic acid, methacrylic acid or a derivative of acrylic acid or methacrylic acid characterised in that the water insoluble copolymer further comprises (b) a copolymerisable sulphonated ethylenically unsaturated comonomer selected from vinyl sulphonic acid, allyl sulphonic acid, methally sulphonic acid, p-styrene sulphonic acid and the salts of these acids, said comonomers (a) and (b) being present in the respective molar percentages in the ranges (a) 26
  • comonomer (b) is effective in adhering the light-sensitive photographic emulsion to the subbing layer.
  • Comonomer (b) also confers anti-static properties upon the coated film base.
  • GB-A 1 146215 relates to a coated article comprising a support of a transparent film of a synthetic polymer having on at least one surface a coating which comprises a copolymer of (A) 70-90 percent by weight of an unsaturated ester of a mono carboxylic acid wherein the alcohol component contains no more than four carbon atoms (B) 7-20 percent by weight of an aliphatic poly-functional compound containing at least two sites of carbon to carbon unsaturation, at least one of which is an allyl or vinyl group, or glycidyl acrylate, glycidyl methacrylate, methacrylate esters wherein the alcohol portion of the ester has a free hydroxy group, orfumaric acid, and (C) 3-30 percent by weight of itaconic acid, fumaric acid, acrylic acid or methacrylic acid, with the proviso that when (B) is fumaric acid (C) is itaconic acid, percentages of the constituents of the copolymer being
  • component (B) indicates that it is intended to act as a copolymerisable cross-linking agent, and by virtue of the requirement that the aliphatic polyfunctional component should include at least two unsaturated functional groups, the definition of component (B) does not embrace the sulphonic acids or salts specified in the present invention.
  • the subbing copolymer for use in accordance with the present invention may be derived from one or more comonomers falling within the aforementioned definitions of each of the comonomers (a) and (b).
  • the self supporting film may be produced from any suitable synthetic linear polyester which may be obtained by condensing one or more dicarboxylic acids or their lower alkyl diesters, e.g. terephthalic acid, isophthalic, phthalic, 2,5-, 2,6- and 2,7-naphthalene dicarboxylic acid, succinic acid, sebacic acid, adipic acid, azelaic acid, diphenyl dicarboxylic acid, and hexahydroterephthalic acid or bis-p-carboxyl phenoxy ethane, optionally with a monocarboxylic acid, such as pivalic acid, with one or more glycols, e.g.
  • dicarboxylic acids or their lower alkyl diesters e.g. terephthalic acid, isophthalic, phthalic, 2,5-, 2,6- and 2,7-naphthalene dicarboxylic acid, succinic acid, sebacic acid, adip
  • Polyethylene terephthalate films are particularly preferred especially those films which have been biaxially in sequence in two mutually perpendicular directions typically at temperatures in the range 78 to 125 °C and heat set typically at temperatures in the range 150 to 250 °C, e.g. as described in GB patent specification 838 708.
  • the copolymers of the subbing composition are essentially water-insoluble. It will be appreciated that water-soluble copolymers would be dissolved by the aqueous solutions which are normally used for photographic processing, e.g. for development and fixing, thereby destroying the adhesion of the superimposed light-sensitive photographic emulsion layer to the underlying polyester film.
  • the subbing compositions including the water-insoluble copolymers may nevertheless be applied to the polyester film as aqueous dispersions or alternatively as solutions in organic solvents.
  • Comonomer a) for the subbing copolymer is preferably present in an amount 50 to 90 mole % and preferably comprises an ester of acrylic acid or methacrylic acid, especially an alkyl ester wherein the alkyl group contains up to ten carbon atoms such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tertbutyl, hexyl, 2-ethyl, hexyl, heptyl and n-octyl.
  • Copolymers derived from an alkyl acrylate, especially ethyl acrylate, together with an alkyl methacrylate provided particularly effective adhesion between the polyester film and the superimposed light-sensitive photographic emulsion layer.
  • Subbing copolymers comprising an alkyl acrylate, e.g. ethyl acrylate or butyl acrylate, together with an alkyl methacrylate, e.g. methyl methacrylate, desirably in a total molar proportion in the range 55 to 80 mole %, are particularly preferred.
  • the acrylate comonomer of such copolymers is preferably present in a proportion in the range 15 to 45 mole % and the methacrylate comonomer preferably in a proportion exceeding that of the acrylate comonomer generally by an amount in the range 5 to 20 mole %.
  • the methacrylate is preferably present in a proportion in the range 30 to 50 mole %.
  • comonomers falling within the definition of comonomer a) which are suitable for use in the preparation of the subbing copolymer which may be used instead of but are preferably copolymerised as optional additional comonomers together with acrylic acid or methacrylic acid or esters of the acids include acrylonitrile, methacrylonitrile, halo-substituted acrylonitrile, halo-substituted methacrylonitrile, acrylamide, methacrylamide, N-methylol acrylamide, N-ethanol acrylamide, N-propanol acrylamide, N-methylol methacrylamide, N-ethanol methacrylamide, N-methyl acrylamide, N-tertiary butyl acrylamide, hydroxyethyl methacrylate, glycidyl acrylate, glycidyl methacrylate, dimethylamino ethyl methacrylate, itaconic acid, itaconic anhydride and half est
  • Comonomer b) which provides anti-static protection for the subbing layer and has also surprisingly been found to be effective in promoting the adhesion of the photographic emulsion layer preferably comprises a salt and most preferably an alkali metal salt, e.g. a sodium salt. Vinyl sulphonic acid and its salts are especially effective adhesion-promoting comonomers.
  • Comonomers which function to modify the properties of the subbing layer may optionally be included in the production of the subbing copolymer, such as comonomers which promote the adhesion of the subbing layer in the wet and dry state to the polyester film and/or to superimposed light-sensitive photographic emulsion layers especially those comprising gelatin.
  • Itaconic acid and itaconic anhydride are particularly effective comonomers in promoting tenacious adhesion to superimposed gelatin-containing layers and are a preferred comonomer according to this invention.
  • Itaconic acid may be copolymerised in an amount comprising up to 20 mole % of the total comonomeric formulation and preferably in the range 2 to 10 mole %.
  • the adhesion of the subbing layer to the polyester film may be modified by including one or more comonomers having cross-linkable functional groups in the comonomeric recipe for the formation of the subbing copolymer.
  • Epoxy group-containing comonomers such as glycidyl acrylate and glycidyl methacrylate, are particularly effective in providing internal cross-linking within the subbing layer and possibly also cross-linking to the polyester film.
  • a comonomeric amount of 5 to 25 mole %, preferably 15 to 25 mole %, of glycidyl acrylate or glycidyl methacrylate is effective in providing the desired adhesion properties.
  • comonomers include vinyl esters such as vinyl acetate, vinyl chloracetate and vinyl benzoate; vinyl pyridine; vinyl chloride; vinylidene chloride; maleic acid; maleic anhydride; butadiene; styrene and derivatives of styrene such as chloro styrene, hydroxy styrene and alkylated styrenes.
  • styrene and/or a styrene derivative When styrene and/or a styrene derivative are employed as a comonomer they must be present only as a minor monomeric constituent, i.e. the molar proportion of the comonomer a) and b) defined above must exceed the molar proportion of the styrene and/or styrene derivative. Thus, the molar proportion of styrene and/or the styrene derivative must be less than 33.3 mole %.
  • subbing copolymers for use according to the invention include copolymers comprising 15 to 45 mole % of an alkyl acrylate, e.g. ethyl acrylate, 30 to 50 mole % of an alkyl methacrylate, e.g. methyl methacrylate, 10 to 20 mole % of a sulphonated comonomer, e.g. sodium vinyl sulphonate and 7 to 20 mole % of itaconic acid optionally with other comonomers such as glycidyl acrylate or methacrylate in a proportion generally in the range 10 to 20 mole %.
  • a sulphonated comonomer e.g. sodium vinyl sulphonate
  • itaconic acid optionally with other comonomers such as glycidyl acrylate or methacrylate in a proportion generally in the range 10 to 20 mole %.
  • Especially effective subbing copolymers are 40/35/10/15 mole % ethyl acrylate/methyl methacrylate/itaconic acid/sodium vinyl sulphonate; 30/45/10/15 mole % butyl acrylate/methyl methacrylate/itaconic acid/sodium vinyl sulphonate; 25/35/10/ 15/15 mole % ethyl acrylate/methyl methacrylate/itaconic acid/glycidyl methacry- late/sodium vinyl sulphonate; and 20/40/15/10/15 mole % butyl acrylate/methyl methacrylate/glycidyl methacrylate/monomethyl itaconate/sodium vinyl sulphonate.
  • adhesion promoters such as a partially hydrolysed vinyl acetate/vinyl chloride copolymer optionally admixed with a chlorinated phenol, and particulate fillers for providing slip properties.
  • the subbing composition may also contain a cross-linking agent which functions to cross-link the subbing copolymer thereby improving adhesion to the polyester film.
  • the cross-linking agent should preferably be capable of internal cross-linking in order to provide protection against solvent penetration.
  • Suitable cross-linking agents may comprise epoxy resins, alkyd resins, amine derivatives such as hexamethoxymethyl melamine, and/or condensation products of an amine, e.g.
  • melamine diazine, urea, cyclic ethylene urea, cyclic propylene urea, thiourea, cyclic ethylene thiourea, alkyl melamines, aryl melamines, benzo guanamines, guanamines, alkyl guanamines and aryl guanamines, with an aldehyde, e.g. formaldehyde.
  • a useful condensation product is that of melamine with formaldehyde.
  • the condensation product may optionally be alkoxylated.
  • the cross-linking agent may be used in amounts of up to 25% by weight based on the weight of the copolymer in the subbing composition.
  • a catalyst is also preferably employed to facilitate cross-linking action of the cross-linking agent.
  • Preferred catalysts for cross-linking melamine formaldehyde include ammonium chloride, ammonium nitrate, ammonium thiocyanate, ammonium dihydrogen phosphate, ammonium sulphate, diammonium hydrogen phosphate, para toluene sulphonic acid, maleic acid stabilised by reaction with a base, and morpholinium para toluene sulphonate.
  • the subbing composition may be applied to the polyester film as an aqueous dispersion or a solution in an organic solvent by any suitable conventional coating technique such as dip coating, bead coating, reverse roller coating or slot coating.
  • the subbing composition may be applied to the polyester film during or after the completion of the process by which the polyester film is produced.
  • the film may be pretreated or coated in such a way to improve the adhesion of the subbing layer to the film surface.
  • Conventional chemical or physical pretreatments such as coating the film surface with a solution having a swelling, solvent or oxidising action on the film, corona discharge treatment, flame treatment, or ultra-violet light treatment may be used.
  • the plastics film may carry on adhesion-promoting polymeric layer to which the subbing layer according to the invention may be applied.
  • subbing compositions bond with acceptable adhesion to the polyester film surface when applied to the film during the process for its manufacture. Satisfactory adhesion is obtainable by direct application of the subbing composition to the polyester film surface without any pretreatment or interposition of an adhesion-promoting layer.
  • Polyester films are normally manufactured by a process wherein the films are molecularly oriented by stretching in two mutually perpendicular directions.
  • the process is conventionally accomplished by sequentially stretching a flat amorphous polyester film first in one direction and then in another mutually perpendicular direction.
  • the stretched films may also be dimensionally stabilised by heat-setting under dimensional restraint. Stretching and heat setting is conventionally carried out by heating the film above ambient temperature.
  • the preferred polyester films for use according to the invention may be made according to such a process.
  • Polyethylene terephthalates are preferably produced by sequential biaxial orientation and heat setting, e.g. as described in GB patent specification 838 708.
  • Polyester films oriented by sequential stretching may be coated with the subbing composition either before stretching in the first direction of stretching or at a stage intermediate the stretching in the first direction and stretching in the second direction. It is preferred according to this invention that the subbing composition should be applied to the film between the two stretching operations, e.g. by firstly stretching the film in the longitudinal direction over a series of rotating rollers, coating with the subbing composition and then stretching transversely in a stenter oven followed by heat-setting.
  • Subbing compositions applied to the polyester film surface are preferably applied as aqueous dispersions.
  • the temperatures applied to the coated film during the subsequent stretching and/or heat setting are effective in drying the aqueous medium, or the solvent in the case of solvent-applied compositions, and also in coalescing and forming the coating into a continuous and uniform subbing layer.
  • the cross-linking of cross-linkable subbing compositions is also achieved at such stretching and/or heat-setting temperatures.
  • the subbing layer is preferably applied to the polyester film at a coat weight within the rang 0.1 to 10 mg/dm 2 , especially 1.0 to 3.0 mg/dm z .
  • each layer preferably has a coat weight within the preferred range.
  • a light-sensitive photographic emulsion layer e.g. a conventional X-ray or graphic arts gelatinous silver halide emulsion
  • a conventional gelatinous subbing layer between the copolymeric subbing layer and the light-sensitive photographic emulsion layer.
  • adequate wet and dry adhesion can be obtained in the absence of a gelatinous subbing layer and by adhering the light-sensitive photographic emulsion layer directly to the copolymeric subbing layer.
  • Modification of the surface of the copolymeric subbing layer may improve the adhesion of a light-sensitive photographic emulsion layer applied directly to the copolymeric subbing layer but may not be essential to the provision of satisfactory adhesion.
  • the preferred treatment by corona discharge may be effected in air at atmospheric pressure with conventional equipment using a high frequency, high voltage generator, preferably having a power output of from 1 to 20 kw at a potential of 1 to 100 kv.
  • Discharge is conveniently accomplished by passing the film over a dielectric support roller at the discharge station at a linear speed preferably of 1.0 to 500 m per minute.
  • the discharge electrodes may be positioned 0.1 to 10.0 mm from the moving film surface.
  • subbing copolymers which provide adequate adhesion without corona discharge treatment are 40/35/10/15 mole % ethyl acrylate/methyl methacrylate/itaconic acid/sodium styrene sulphonate and 41/41.5/8.5/9.0 mole % ethyl acrylate/ methyl methacrylate/glycidyl methacrylate/sodi- um styrene sulphonate.
  • the light-sensitive photographic emulsion may optionally include any of the conventional additives.
  • the coated film bases also have excellent anti- static properties such that they pass effectively and without interruption through coating machines, e.g. for the application of light-sensitive photographic emulsions.
  • Dry adhesion refers to the adhesion of a gelatinous silver halide emulsion to the plastics film in the final photographic film, assessed, both before and after processing in standard photographic chemicals, by sticking a self-adhesive tape along the torn edge of the film and rapidly separating the tape from the film.
  • Wet adhesion refers to the adhesion of a gelatinous silver halide emulsion to the plastics film in the final photographic film, assessed, after processing in the standard photographic chemicals and washing in water for 15 minutes by rubbing with a sponge over a series of lines scored in the still wet emulsion.
  • An aqueous dispersion of an ethyl acrylate/methyl acrylate/itaconic acid/sodium vinyl sulphonate copolymer of respective proportions 40/35/10/15 mole % was prepared by conventional emulsion polymerisation of the following ingredients:
  • a subbing composition was produced from the resulting aqueous dispersion as a mixture of the ingredients:
  • a polyethylene terephthalate film was melt extruded, cast onto a coated rotating drum and stretched in the direction of extrusion to about three times its original dimension in that direction by conventional procedure and was coated on both sides with a uniform layer of the aqueous subbing composition.
  • the coated film was passed into a heated stenter oven where the coatings were dried and the film stretched about three times its original dimension in the transverse direction in a conventional manner.
  • the film was then heat set under dimensional restraint at a temperature of about 200°C by conventional procedure.
  • the applied subbing layers were formed into uniform continuous layers each having a dry coat weight of approximately 1.5 mg/dm 2 and the film had an overall thickness of about 100 ⁇ m.
  • the subbing layers were then coated with a conventional silver halide X-ray emulsion which was chilled to gel the coating and dried for 20 minutes at 33°C.
  • the dry and wet adhesions of the silver halide emulsion layers to the polyethylene terephthalate film were determined by the tests noted above and were found to be strong and acceptable for photographic use.
  • the subbed film was found to have excellent antistatic properties when tested at a temperature of 20°C and a relative humidity of 60% and before the application of the silver halide emulsion layers, i.e. a surface resistivity of 1.6xlO' O ohms/square.
  • Example 1 was repeated using similar aqueous dispersions but containing different subbing copolymers as shown in the following Table, with the exception that the hexamethoxy methyl melamine component was omitted from the composition for Example 3.
  • the subbing layers Prior to the application of the silver halide X-ray emulsions, the subbing layers were subjected to corona discharge treatment by passing the film at 6.1 metres per minute through a commercially available "Vetaphone” (trademark) 3 kw treater using a power of 2 kw and electrode to film distance of 1 mm.
  • Vetaphone commercially available "Vetaphone” (trademark) 3 kw treater using a power of 2 kw and electrode to film distance of 1 mm.
  • the subbed films were found to have excellent antistatic properties, represented by the surface resistivities noted in the Table when measured at a temperature of 20°C and a relative humidity of 60%.
  • aqueous subbing latex was prepared by conventional emulsion polymerisation of the following monomeric mixture:
  • the latex was prepared by adding 306 g of the monomeric mixture together with 18.5 ml of an emulsifier comprising nonyl phenol condensed with 12 moles of ethylene oxide, 22.5 g of sodium dodecyl benzene sulphonate and 2 g of potassium persulphate to one litre of water.
  • an emulsifier comprising nonyl phenol condensed with 12 moles of ethylene oxide, 22.5 g of sodium dodecyl benzene sulphonate and 2 g of potassium persulphate
  • a polyethylene terephthalate film was melt extruded and quenched to the amorphous state on a cooled rotating drum. The resulting film was stretched in the direction of extrusion to about 3.5 times its original length. It was then coated on both sides with the aqueous latex prepared above by a roller coating technique and passed into a stenter oven where the coating was dried. The dried coated film was then stretched sideways about 3.5 times its original width and finally heat set at a temperature of about 210°C. The final thickness of the coating on each side of the biaxially drawn film was about 0.2 micrometer, and the total thickness of the coated film was about 100 micrometers.
  • the subbed film had a surface resistivity of about 10 11 ohms/square at 20°C and a relative humidity of 60%.
  • the copolymeric subbing layers were then coated directly with a conventional gelatinous silver halide photographic emulsion without prior treatment by corona discharge and tested for dry and wet adhesion. The adhesions were strong in each case.

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  • Spectroscopy & Molecular Physics (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)

Claims (11)

1. Matériau photographique comprenant (1) un film autoporteur en polyester linéaire synthétique (2) une couche d'ancrage continue appliquée sur au moins une surface de ce film autoporteur et (3) une couche à émulsion photographique photosensible appliquée directement ou indirectement sur la couche d'ancrage, laquelle couche d'ancrage comprend un copolymère insoluble dans l'eau comprenant (a) un comonomère choisi parmi l'acide acrylique, l'acide méthacrylique ou un dérivé d'acide acrylique ou d'acide méthacrylique, caractérisé en ce que le copolymère de la couche d'ancrage comprend de plus (b) un comonomère à insaturation éthylénique sulfoné copolymérisable choisi parmi l'acide vinylsulfonique, l'acide allylsulfonique, l'acide méthallylsulfonique, l'acide p-styrènesulfonique et les sels de ces acides, ces comonomères (a) et (b) étant présents selon des pourcentages molaires respectifs compris dans les gammes (a) de 26 à 99% et (b) de 1 à 50%.
2. Matériau photographique suivant le revendication 1, dans lequel le comonomère (a) comprend un mélange d'acrylate d'alcoyle et de méthacrylate d'alcoyle selon une proportion molaire totale comprise dans une gamme allant de 55 à 80 moles %.
3. Matériau photographique suivant la revendication 2, dans lequel le comonomère (a) comprend un mélange de 15 à 45 moles % de l'acrylate d'alcoyle et de 30 à 50 moles % du méthacrylate d'alcoyle.
4. Matériau photographique suivant l'une quelconque des revendications précédentes, dans lequel le copolymère d'ancrage est dérivé d'un ou plusieurs comonomères additionnels choisi parmi l'acide itaconique, l'anhydride itaconique, les hémi-esters d'acide itaconique, l'acrylate glycidylique et le méthacrylate glycidylique.
5. Matériau photographique suivant la revendication 3, dans lequel le copolymère d'ancrage comprend de 15 à 45 moles % d'acrylate d'alcoyle/30 à 50 moles % de méthacrylate d'alcoyle/10 à 20 moles % de comonomère sulfoné/7 à 20 moles % d'acide itaconique.
6. Procédé pour la production d'un matériau photographique photosensible, consistant à appliquer une couche d'ancrage continue sur au moins une surface d'un film autoporteur en polyester linéaire synthétique et à appliquer une couche d'émulsion photographique photosensible directement ou indirectement sur la couche d'ancrage, selon lequel la couche d'ancrage est appliquée à partir d'une composition filmogène comprenant un copolymère insoluble dans l'eau qui comprend (a) un comonomère choisi parmi l'acide acrylique, l'acide méthacrylique ou un dérivé d'acide acrylique ou d'acide méthacrylique, caractérisé en ce que le copolymère insoluble dans l'eau comprend de plus (b) un comonomère à insaturation éthylénique sulfoné copolymérisable choisi parmi l'acide vinylsulfonique, l'acide allylsulfonique, l'acide méthallylsulfonique, l'acide p-styrènesulfonique, et les sels de ces acides, ces comonomères (a) et (b) étant présents selon les pourcentages molaires respectifs compris dans les gammes (a) de 26 à 99% (b) de 1 à 50%.
7. Procédé suivant la revendication 6, dans lequel le comonomère (a) comprend un mélange d'un acrylate d'alcoyle et d'un méthacrylate d'alcoyle, selon une proportion molaire totale comprise dans une gamme allant de 55 à 80 moles %.
8. Procédé suivant la revendication 7, dans lequel le comonomère (a) comprend un mélange de 15 à 45 moles % de l'acrylate d'alcoyle et de 30 à 50 moles % du méthacrylate d'alcoyle.
9. Procédé suivant l'une quelconque des revendications 6 à 8, dans lequel le copolymère d'ancrage est dérivé d'un ou plusieurs comonomères additionnels choisis parmi l'acide itaconique, l'anhydride itaconique, les hémi-esters d'acide itaconique, l'acrylate glycidylique et le méthacrylate glycidylique.
10. Procédé suivant la revendication 9, dans lequel le copolymère d'ancrage comprend de 15 à 45 moles % d'acrylate d'alcoyle/de 30 à 50 moles % de méthacrylate d'alcoyle/de 10 à 20 moles % de comonomère sulfoné/de 7 à 20 moles % d'acide itaconique.
11. Procédé suivant l'une quelconque des revendications 6 à 10, dans lequel la surface de la couche d'ancrage est soumise à un traitement par effluves avant l'application directe sur celle-ci de la couche d'émulsion photographie photosensible.
EP19800300759 1980-03-12 1980-03-12 Films photographiques avec une couche adhésive et procédés pour leur fabrication Expired EP0035614B2 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP19800300759 EP0035614B2 (fr) 1980-03-12 1980-03-12 Films photographiques avec une couche adhésive et procédés pour leur fabrication
DE8080300759T DE3067999D1 (en) 1980-03-12 1980-03-12 Improvements in coated film bases, photographic films derived from the bases and processes for their production

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Application Number Priority Date Filing Date Title
EP19800300759 EP0035614B2 (fr) 1980-03-12 1980-03-12 Films photographiques avec une couche adhésive et procédés pour leur fabrication

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EP0035614A1 EP0035614A1 (fr) 1981-09-16
EP0035614B1 EP0035614B1 (fr) 1984-05-30
EP0035614B2 true EP0035614B2 (fr) 1988-01-07

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Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4571363A (en) * 1983-12-12 1986-02-18 American Hoechst Corporation Polyester film primed with crosslinked acrylic polymers
GB8925095D0 (en) * 1989-11-07 1989-12-28 Ici Plc Polymeric film
JPH08248570A (ja) * 1995-02-17 1996-09-27 Eastman Kodak Co 写真要素
US5618657A (en) * 1995-02-17 1997-04-08 Eastman Kodak Company Photographic silver halide element having polyester support and exhibiting improved wet adhesion
US6162597A (en) * 1999-12-17 2000-12-19 Eastman Kodak Company Imaging elements adhesion promoting subbing layer for photothermographic imaging layers
US6165699A (en) * 1999-12-17 2000-12-26 Eastman Kodak Company Annealed adhesion promoting layer for photographic imaging elements
GB0015622D0 (en) * 2000-06-26 2000-08-16 Dupont Teijin Films U S Limite Polymeric film
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US3460982A (en) * 1966-01-03 1969-08-12 Du Pont Biaxially oriented polyester film base having a sublayer of an alkyl acrylate/diallyl phthalate/itaconic acid
US3488249A (en) * 1966-06-15 1970-01-06 Du Pont Laminating adhesives and laminates
JPS5473871A (en) * 1977-11-24 1979-06-13 Fuji Photo Film Co Ltd Undercoating of polyester film

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EP0035614A1 (fr) 1981-09-16
DE3067999D1 (en) 1984-07-05
EP0035614B1 (fr) 1984-05-30

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