|Publication number||US3754924 A|
|Publication date||Aug 28, 1973|
|Filing date||May 3, 1971|
|Priority date||Jun 4, 1970|
|Also published as||CA982392A, CA982392A1, DE2124262A1, DE2124262C2|
|Publication number||US 3754924 A, US 3754924A, US-A-3754924, US3754924 A, US3754924A|
|Inventors||Geest W De, H Vandenabeele|
|Original Assignee||Agfa Gevaert Nv|
|Export Citation||BiBTeX, EndNote, RefMan|
|Referenced by (50), Classifications (10)|
|External Links: USPTO, USPTO Assignment, Espacenet|
iJniie States Patent 1191 De Geest et a1.
[ PHOTOGRAPHIC SILVER HALIDE ELEMENT WITH AN ANTISTATIC OUTER LAYER COMPRISING A FLUORINATED SURFACTANT AND A POLYMETHACRYLATE MATTING AGENT  Inventors: Wilfried Florent De Geest, Berchem; Hubert Vandenabeele, Wilrijk, both of Belgium  Assignee: AGFA-Gevaert N.V., Mortsel,
Belgium  Filed: May 3, 1971  Appl. No.: 139,930
 Foreign Application Priority Data June 4, 1970  US. Cl 96/ll4.2, 96/67, 96/114.5  int. C1. G03c 1/02, G030 l/38, G03c 7/00  Field of Search 96/94, 114.2, 114.5,
 References Cited UNITED STATES PATENTS 2,732,398 1/1956 Brice 252/71 Great Britain 27,048/70 1451 Aug. 28, 1973 2,937,098 5/1960 Geen 260/292 U 3,516,835 6/1970 Mackey 96/114.S 3,589,906 6/1971 McDowell 96/1145 3,631,514 12/1971 Lee 96/87 A OTHER PUBLICATIONS Surface Active Materials From Perfluorocarboxylic and Perfluorosulfonic Acids," Guenther, 1nd. & Eng. Chem., Vol. 1, No. 3, pp. 165-169 (1962).
Primary Examiner-Norman G. Torchin Assistant Examiner-Alfonso T. Suro Pico Attorney-Alfred W. Breiner  ABSTRACT 21 Claims, No Drawings PHOTOGRAPHIC SILVER HALIDE ELEMENT WlTH AN ANTISTATIC OUTER LAYER COMPRISING A FLUORINATED SURFACTANT AND A POLYMETHACRYLATE MATTI NG AGENT The present invention relates to photographic silver halide elements having outer coatings with improved surface and antistatic properties.
It is known that discrete solid particles of waterinsoluble inorganic or organic materials, called matting agents, can be used in a protective layer over the silver halide emulsion layer of a photographic element and/or in a backing layer at the rear of the support of said element to provide rough surfaces which are often desirable in the photographic art. Examples of inorganic matting agents are silicon dioxide, titanium dioxide, magnesium oxide, aluminium oxide,'barium sulphate, calcium carbonate, glass, etc. Examples of organic matting agents are starch, cellulose esters such as cellulose acetate propionate, cellulose ethers such as ethyl cellulose, synthetic resins such as polymeric esters of acrylic and methacrylic acid for example polymethyl methacrylate, polyvinyl resins such as polyvinyl acetate, polycarbonates, homoand copolymers of styrene, etc. These matting agents may be used in order to reduce the sticking tendency of the photographic material for example when the material is stored or packed in the form of a roll or stack. They may be used to provide sufficient surface roughness to prevent the formation of Newtons rings when printing and enlarging in that the contact surface of the photographic material with another material is relatively small. Further, they may be used to decrease abrasion by dry-friction and to reduce the tendency of scratching when materials are stored or packed in contact with other material as is the case e.g. with X-ray material packed without interleaves. It is also possible to use matting agents in order to obtain the desired coefficient of friction for film materials intended for use in apparatus for rapid handling and transport. Moreover, matting agents may have in some cases a slight effect in reducing the generation of static electricity in photographic elements, since a rough surface is obtained and therefore the contacting surface of the photographic element with other materials, which might cause static discharges, is reduced.
Owing to the generation of static electricity a large number of difficulties are encountered during the preparation and use of photographic elements, especially film elements. The generation of static electricity may be caused by rubbing of the film element against rollers and other elments through or on which the film materials are guided, by contact of the film element with rough surfaces or by many other known reasons. Discharges of static electricity in an unprocessed photographic element cause local film exposure and on processing said element the discharge images become visible in the form of irregular streaks or lines and black spots. Discharges in a processed film element, especially in film material for cinematographic purposes, are also undesirable since friction of the film material against elements of the projection apparatus is thereby enhanced.
Matting agents have a poor antistatic effect and therefore if it is the intention to effectively reduce the generation of static electricity, the outer coatings provided as protective coating over a radiation-sensitive silver halide emulsion layer or as backing layer at the rear of the support generally comprise compounds known as antistatic agents.
Antistatic agents, however, have an influence on the coating characteristics of the hydrophilic colloid composition when used therein; for instance they may reduce the coating quality such as the uniformity of coating and may give rise to the formation of streaks and repellency spots or comets. The coating quality can, of course, be improved by appropriate choice of surface active compounds as coating aid such as saponine, aliphatic sulphates, sulphonates and carboxylates, which may comprise alkylene oxide units, etc. but these coating aids in their turn often reduce the antistatic properties of the hydrophilic colloid coating in which they are incorporated.
in Belgian Patent Specification No. 742,680 filed Dec. 5, 1969 by Gevaert-Agfa N.V. fluorinated surfactants have been described for use as coating aids in hydrophilic colloid coating compositions. By the use of these fluorinated surfactants instead of known coating aids or in addition thereto it was found possible to reduce or eliminate the disadvantageous efiect of known coating aids on the antistatic properties while retaining favourable coating qualities.
It has now been found that the favourable effect of these fluorinated surfactants in reducing the generation of static electricity in a hydrophilic colloid outer coating of a photographic silver halide element, can still be improved by addition of solid water-insoluble particles of matting agents to the coating composition of the said outer coating.
We found that the simultaneous use in photographic silver halide elements of matting agents, which themselves have only a poor antistatic effect, and fluorinated surfactants, which have better antistatic properties than matting agents, could provide substantially superior antistatic properties than was to be expected knowing the effects of both agents alone. This is illustrated in the Examples hereinafter.
By the combined use of a matting agent and a fluorinated surfactant optimum triboelectric properties are obtained for the photographic element with regard to conventional materials such as paper, stainless steel, rubber, synthetic resins, etc. that come into contact with the said element.
In accordance with the present invention there is provided a photographic radiation-sensitive silver halide element, which comprises a radiation-sensitive silver halide emulsion layer and an outer coating of a hydrophilic colloid, wherein the said outer coating comprises a fluorinated surfactant as well as a matting agent.
The invention is especially concerned with the improvement of the antistatic properties of hydrophilic colloid protective coatings coated over a radiationsensitive silver halide emulsion layer and is of particular value in the manufacture of X-ray material, more especially double coated X-ray material and other double coated films where both sides of the film support e.g. a cellulose triacetate or polyethylene terephthalate support are provided with radiation-sensitive silver halide emulsion layers and hydrophilic colloid protective coatings as outer layers.
The matting agents of use according to the present invention may be of inorganic as well as organic nature, examples of which have been given before. it is also possible to use a combination of at least two different matting agents for instance matting agents differing from one another in hardness, one being relatively soft such as polymethylmethacrylate and another being relatively hard such as silicon dioxide.
The matting agents of use according to the present invention are incorporated into the hydrophilic colloid coating composition of the outer coating, more especially a protective coating to be applied over the photographic silver halide emulsion layer, using any method which will achieve uniform dispersion of the particles in the layer. The. matting agents may be used in amounts varying between very wide limits. In general, the matting agents can be used, per side of support, at a total coverage in the range 'of about 10 mg to about 100 mg per sq.m, although larger amounts may also be used. The matting agent particles generally have a particle diameter comprised between about 1 and about l microns, preferably at least 50 percent of the matting agent particles have a diameterin the range of 4 to 7 microns.
Photographic elements containing matting agents in an outer layer generally exhibit especially good resistance to abrasion, a reduced sticking tendency of the element when it is stored or packed in the form of a roll or stack and a favourable coefficient of friction for use in apparatus for rapid handling and transport. However, the presence of matting agent particles in such an outer layer sometimes causes turbidity so that a processed silver image has a milky appearance. This situation can be corrected by incorporating into the outer layer polycarbocyclic aromatic sulphonic acids or wa- A stands for a chemical bond or a bivalent hydrocarbon group, preferably an aliphatic, aromatic or mixed aliphatic-aromatic group including such bivalent hydrocarbon group interrupted by heteroatoms, such as oxygen, ester groups (COO) and I amide groups (CONR- and SO NR wherein R=H or C,C,, alkyl), and X stands for a hydrophilic group for example a hydrophilic nonionic polyoxyalkylene group such as a' polyoxyethylene group of the formula (Cl l Cl-l O),.R
wherein R, stands for hydrogen or alkyl comprising whereinAlk. stands for lower alkylene comprising from one to five carbon atoms such as methylene, ethylene, propylene and butylene and R stands for lower alkyl comprising from one to five C-atoms such as methyl and ethyl, and preferably a hydrophilic anionic group ter-soluble salts thereof as described in Belgian Patent Specification 738,856 filed Sept. 15, 1969 by Gevaert- Agfa NV.
The hydrophilic colloid of the outer coating preferably comprises gelatin as hydrophilic colloid though other hydrophilic colloidal materials or mixtures of them, e.g. hydrophilic natural colloids, modified hydrophilic natural colloids or synthetic hydrophilic polymers may also be used. More particularly these colloids may be selected of such film-forming natural or modified natural hydrophilic colloids as e.g. glue, casein,
, zein, hydroxy-ethyl cellulose, carboxymethyl cellulose,
methyl cellulose, carboxymethyl hydroxyethyl cellulose, gum arabic, sodium alginate and hydrophilic derivatives of such colloids. They-may also be selected of such synthetic hydrophilic polymers as e.g. polyvinyl alcohol, poly-N-vinyl pyrrolidone, polyvinyl amine, polyethylene oxide, polystyrene sulphonic acid, polyacrylic acid, and hydrophilic copolymers and derivatives of such polymers.
The fluorinated surfactants for use in accordance with the present invention comprise, as described in wherein I R stands for a partly or wholly fluorinated hydrocarbon chain comprising at least three fluorine atoms,
such as the groups SO:,M, -OSO M,' --COOM,
wherein M stands for hydrogen, an alkali metal atom such as sodium and potassium, an ammonium group or an organic ammonium groups such as diethanolammonium, morpholinium, pyridinium etc. and R stands for an alkyl group or the group R The sum of the number of F-atoms, in the group R; plus the number of C-atoms in the fluorinated hydrocarbon chain of R and the number of C-atoms in the hydrocarbon group of A (if any) is preferably at least equal to 10. In accordance with the present invention best results'are obtained with fluorinated surfactants having a terminal trifluoromethyl group.
Representative examples of fluorinated surfactants suitable for use according to the present invention and corresponding to the above general fonnula are l HOINU The fluorinated surfactants for use in combination with matting agents in order to improve the antistatic properties of hydrophilic colloid outer coatings need not necessarily be provided in the coating composition for forming said outer coating comprising the matting agent. As a matter of fact, it is also possible to incorporated the fluorinated surfactants in the coating composition of an underlying water-permeable colloid layer such as a silver halide emulsion from which they can diffuse to the surface of the outer coating when the composition for forming the latter is applied on the wet or gellified but not yet dried underlying layer. Alternatively, the fluorinated surfactant may be incorporated into both the coating composition for forming the outer coating and the coating composition for forming an underlying water-permeable colloid layer for instance both in the radiation-sensitive silver halide emulsion and the hydrophilic colloid coating compositions for being coated thereover.
The fluorinated surfactants are generally used in amounts comprised between about 0.1 and about 2 percent by weight relative to the amount of dry colloid of the layer into which the said fluorinated surfactants are incorporated.
Protective colloid compositions for being coated over radiation-sensitive silver halide emulsion layers comprising matting agents and fluorinated surfactants, of which the latter can be present therein by direct incorporation or by diffusion from underlying silver halide emulsion layers may comprise all sorts of other materials conventionally used in said protective layers. For instance, they may comprise plasticizers, filling agents, hardening agents such as formaldehyde and mucochloric acid, hardening accelerators such as resorcin, polyvinyl lactams and polyvinyl lactones such as poly-N-vinyl pyrrolidone and polyvinyl-2-oxazolidone as antifoggants, antistatic agents e.g. polyoxyalkylene compounds for example alkoxylated alcohols and phenols such as ethoxylated alkyl phenols, ethoxylated castor oil, polyoxyalkylene esters of fatty acids such as the polyoxyethylene glycol (molecular weight about 300) ester of oleic acid, urethans or esters of the above alkoxylated hydroxy compounds e.g. those of the kind described in Belgian Patent Specification 706,563 filed Nov. 16, 1967 by Gevaert-Agfa N.V. such as the nonylphenoxy triethyleneoxyethyl ester of carbanilic acid. They may further comprise conventional coating aids such as saponine, dialkyl sulphosuccinic acid salts such as sodium diisooctylsulphosuccinate and salts of alkyl sulphuric acids, salts of alkyl sulphonic acids, salts of alkylaryl polyether sulphuric acids and salts of alkylaryl polyether sulphonic acids, carboxyalkylated polyethylene glycol ethers or esters, etc.
The silver halide employed in the preparation of the radiation-sensitive silver halide emulsion layer(s) of the photographic element according to the present invention includes any of the photographic silver halides as exemplified by silver bromide, silver iodide, silver chloride or mixed silver halides e.g. silver chlorobromide and silver bromoiodide.
These siliver halides are dispersed in the common hydrophilic colloids or mixtures of colloids, examples of which are given above, gelatin being, however, favoured.
The support may be any conventional transparent or opaque support as normally used in the art such as paper, glass and film. The invention, however, is of particular advantage in those cases where transparent film supports are used such as films of cellulose esters for instance cellulose triacetate, and films of polyesters for instance polyethylene terephthalate.
The emulsion can contain the usual additives including for example, stabilizers or antifoggants such as inorganic acid salts of cadmium, cobalt and manganese and substituted triazoindolizines, speed increasing addenda such as alkylene oxide polymers and onium compounds for instance quaternary ammonium compounds, gelatin hardeners, plasticizersand the like. The emulsions may be spectrally sensitized emulsions as well as not spectrally sensitized emulsions.
The following examples illustrate the present invention.
EXAMPLE I A gelatino silver bromoiodide (2 mole of iodide) X-ray emulsion comprising per kg 80 g of gelatin and an amount of silver halide corresponding to 190 g of silver nitrate was coated on both sides of a subbed cellulose triacetate support pro rata of about 27 sq.m (per side of support) per kg of emulsion.
At both sides of the support, the emulsion layers while still wet were overcoated with a gelatin antistress layer from an aqueous gelatin composition comprising per litre 30 g of gelatin, 28 ml of a 5 percent aqueous solution of sodium diisooctyl sulphosuccinate as coating aid, an antistatic agent as well as the additives listed in the table below.
The gelatin antistress layers were coated pro rata of about 27 sq.m per litre of aqueous gelatin composition which means that per sq.m and per side of support about 1.1 g of gelatin was present.
The antistatic properties of the antistress layers were detennined on the one hand by measuring the triboelectric charging of the photographic X-ray film material by rubbing against rubber, packaging or interleave paper and brass (the values listed in the table for this triboelectric charging are expressed in pico Coulomb) and on the other hand by estimating the discharge images produced in the emulsion layer by the sparks formed on rubbing the material against rubber, brass, polyvinyl chloride and intensifying lead screens. For the latter purpose, the light-sensitive material is rubbed against rubber, brass, polyvinyl chloride and intensifying lead screens in the dark whereupon the lightsensitive material is developed to make visible the discharge images produced. The values given for the sparks should be interpreted as follows 0 stands for excellent, 1 stands for very good, 2 stands for good, 3 stands for unsatisfactory and 4 stands for poor behaviour against formation of sparks.
The results attained are listed in the table below.
TABLE Additives to antistress Triboelectric charging The above results clearly show the unexpectable, favourable effect on the electrostatic properties of the combination of matting agents with fluorinated surfactants. For instance, while both the polymethylmethacrylate and the fluorinated surfactant have only a slight effect on the triboelectric charging by rubbing against brass, this charging is markedly reduced by using both agents together. Though, on rubbing against rubber, the matting agent increases the chargeability, the overall effect of the use of both agents together results in a reduction of the triboelectric charging which is higher than the reduction obtained with the fluorinated surfactant alone. The same favourable effectoccurs when using as fluorinated surfactant compounds 4, 22, 24 and 25.
EXAMPLE 2 This example shows that the same effects as described in example 1 are obtained when the fluorinated surfactant is incorporated in the silver halide emulsion 55 layer.
A silber bromoiodide X-ray emulsion comprising per kg g of gelatin, an amount of silver halide corresponding to g of silver nitrate and 6 ml of a 5 percent aqueous solution of the coating aid with formula iSOCgI-hyQ-(O C IIZCI'IDBO CH C O ONa was coated on both sides ofa subbed cellulose triacetate support pro rata of about 27 sq.m (per side of support) per kg of emulsion.
At both sides of the support, the emulsion layers, while still wet, were overcoated with a gelatin antistress layer from an aqueous composition comprising per litre 30 g of gelatin, 28 ml of a percent aqueous solution of sodium diisooctylsulphosuccinate as coating aid, and an antistatic agent.
The gelatin antistress layers were coated pro rata of about 27 sq.m per litre of aqueous gelatin composition which means that per sq.m and per side of support about 1.1 g of gelatin was present.
The antistatic properties of the material A thus obtained were compared with the antistatic properties of a material B prepared in the same way with the only difference that the antistress coating composition also comprised per litre, 1 g of polymethyl -methacrylate particles as described in example 1 and with the antistatic properties of a material C prepared in the same way as material B but with the further difference that the silver halide emulsion comprised per kg 2 ml of a 5 percent aqueous solution of the fluorinated surfactant re ferred to in the table of example 1.
The following results were attained.
Material Triboelectrrc charging (pico Coulomb) by rubbing against bras rubber intensifying lead screens A 8100 27000 I 100 B 7900 28000 1200 C 4300 19000 l500 We claim:
1. A photographic element comprising a radiationsensitive silver halide emulsion layer and a hydrophilic colloid outer layer wherein said outer layer comprises a fluorinated surfactant as well as solid, water-insoluble discrete particles of polymethylmethacrylate as matting agent, said surfactant having at least one hydrophilic anionic group, hydrophilic non-ionic group or hydrophilic betaine group and one or more hydrocarbon chain(s) at least one of which is a C, to C hydrophobic hydrocarbonchain, the hydrogen atoms of one or more of the said hydrocarbon chain(s) being wholly or partly replaced by fluorine.
2. A photographic element according to claim 1, wherein the particles of said polymethylmethacrylate have a diameter of from about 1 and about microns.
3. A photographic element according to claim 1, wherein at least 50 percent of the said particles have a diameter in the range of from about 4 to 7 microns.
4. A photographic element according to claim 1, wherein said matting agent is used at atotal coverage per side of the support, in the range of about 10 mg to about 100 mg per sq.m.
5. A photographic element according to claim 1, wherein said fluorinated surfactant corresponds to the formula R,P A X wherein R stands for a partly or wholly fluorinated hydrocarbon chain comprising at least three fluorine atoms,
A stands for a chemical bond or a bivalent hydrocar bon group including a bivalent hydrocarbon group interrupted by one or more hetero atoms or by the group -COO, -CON(R)- or SO,N(R) wherein R is hydrogen or alkyl comprising from one to five C-atoms,
X stands for a hydrophilic non-ionic polyoxyalkylene group, a hydrophilic anionic group selected from SO M, -OSO,M, COOM,
wherein M stands for hydrogen, an alkali metal atom, an ammonium group or an organic ammonium group and R stands for an alkyl group or the group R or a hydrophilic betaine group selected from the group consisting of wherein R, stands for lower alkyl comprising from one to five C-atorns and Alk. stands for lower alkylene comprising from one to fiveC-atoms.
6. A photographic element according to claim 5, wherein the sum of the number of F-atoms in the group R plus the number of C-atoms in the fluorinated hydrocarbon group of R and the number of C-atoms in the hydrocarbon group of A (if any) is at least equal to 10.
7. A photographic element according to claim 1, wherein the fluorinated surfactant comprises a terminal trifluormethyl group.
8. A photographic element according to claim- 1, wherein said fluorinated surfactant is a perfluorocarboxylic acid in acid or salt form.
9. A photographic element according to claim 1, wherein the fluorinated surfactant is present in the said outer layer in an amount comprised between 0.1 and 2 percent by weight relative to the amount of dry colloid.
10. A photographic element according to claim 1, wherein the hydrophilic colloid of the said outer layer is gelatin.
11. A photographic element accordinglto claim 1, wherein the said radiation-sensitive silver halide emul- 5 sion layer is a gelatino silver halide X-ray emulsion 12. A photographic element according to claim 1, wherein the said element is a double-coated X-ray film element provided at both sides of the film support with a said radiation-sensitive silver halide emulsion layer and a said hydrophilic colloid outer layer coated over the said emulsion layers.
13. A method of preparing a photographic element having a radiation-sensitive silver halide emulsion layer and a hydrophilic colloid outer layer, which comprises incorporating a fluorinated surfactant into the said outer layer or into an underlying hydrophilic colloid layer from which the said fluorinated surfactant can diffuse towards the surface of said outer layer, and in corporating solid, water-insoluble discrete particles of .placed by fluorine.
14. A method according to claim 13, wherein said particles have a diameter comprised between about I and about l microns.
15. A method according to claim 13, wherein at least 50 percent of the said particles have a diameter in the range of about 4 to about 7 microns.
16. A method according to claim 13, wherein the said polymethylmethacrylate is incorporated in the said outer layer at a total coverage per side of support, in the range of about 10 mg to about 100 mg per sq.m.
17. A method according to claim 13, wherein said fiuorinated surfactant corresponds to the formula wherein M stands for hydi'ogen, an alkali metal atom, an ammonium group or an organic ammonium group and R stands for an alkyl group or the group R or a hydrophilic betaine group selected from the group consisting of wherein R, stands for lower alkyl comprising from one to five C-atoms and Alk. stands for lower alkylene comprising from one to five C-atoms.
18. A method according to claim 17, wherein the sum of the number of F-atoms in the group R, plus the number of C-atoms in the fluorinated hydrocarbon group of R and the number of C-atoms in the hydrocarbon group of A (if any) is at least equal to l0 19. A method according to claim 13, wherein the fluorinated surfactant comprises a terminr. t-rifluormethyl group. i
20. A method according to claim 13, eherein said fluorinated surfactant is a perfluorocarboxylic acid in acid or salt form.
21. A method according to claim 13, wherein the fluorinated surfactant is incorporated into the said outer layer or the said underlying hydrophilic colloid layer in an amount comprised between 0.1 and 2 percent by weight relative to the amount of dry colloid.
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3833368 *||Dec 4, 1972||Sep 3, 1974||Polaroid Corp||Photographic products incorporating anti-reflection coatings|
|US3861924 *||Feb 9, 1973||Jan 21, 1975||Gaf Corp||Improvement in viscosity of gelatin solutions for photosensitive materials|
|US3948663 *||Aug 27, 1974||Apr 6, 1976||Fuji Photo Film Co., Ltd.||Multi-layer color photographic light-sensitive material|
|US4013472 *||Jan 16, 1975||Mar 22, 1977||Fuji Photo Film Co., Ltd.||Photographic light-sensitive material|
|US4050940 *||Mar 10, 1976||Sep 27, 1977||Konishiroku Photo Industry Co., Ltd.||Process for the preparation of a photographic material|
|US4172731 *||Apr 3, 1978||Oct 30, 1979||Eastman Kodak Company||Photographic element containing a light absorbing matting agent|
|US4201586 *||Nov 4, 1977||May 6, 1980||Fuji Photo Film Co., Ltd.||Photographic light-sensitive material|
|US4242444 *||Jun 30, 1978||Dec 30, 1980||Konishiroku Photo Industry Co., Ltd.||Process for the preparation of light-sensitive silver halide photographic material|
|US4267255 *||Dec 12, 1979||May 12, 1981||Polaroid Corporation||Novel photographic processing composition|
|US4267265 *||Dec 29, 1978||May 12, 1981||Fuji Photo Film Co., Ltd.||Photographic light-sensitive material|
|US4335201 *||Nov 24, 1980||Jun 15, 1982||Eastman Kodak Company||Antistatic compositions and elements containing same|
|US4347308 *||Feb 17, 1981||Aug 31, 1982||Fuji Photo Film Co., Ltd.||Photographic materials|
|US4385110 *||Aug 26, 1981||May 24, 1983||Fuji Photo Film Co., Ltd.||Process for preparing color photographic light-sensitive materials|
|US4415626 *||Jan 8, 1982||Nov 15, 1983||Eastman Kodak Company||Antistatic composition and elements and processes utilizing same|
|US4504567 *||Aug 9, 1984||Mar 12, 1985||Konishiroku Photo Industry Co., Ltd.||Light-sensitive lithographic printing plate|
|US4508764 *||Dec 14, 1982||Apr 2, 1985||E. I. Du Pont De Nemours And Company||Coating process employs surfactants|
|US4613520 *||Jan 25, 1985||Sep 23, 1986||Hercules Incorporated||Coating compositions|
|US4614708 *||Feb 16, 1984||Sep 30, 1986||Agfa-Gevaert, N.V.||Method for the preparation of stable aqueous dispersions of polymer beads and the use of these dispersions in photographic elements|
|US4711838 *||Aug 26, 1985||Dec 8, 1987||Minnesota Mining And Manufacturing Company||Photographic elements sensitive to near infrared|
|US4847186 *||Jun 1, 1987||Jul 11, 1989||Fuji Photo Film Co., Ltd.||Silver halide photographic light-sensitive materials|
|US4847187 *||Aug 28, 1987||Jul 11, 1989||Konishiroku Photo Industry Co., Ltd.||Light-sensitive silver halide photographic material|
|US4975363 *||Nov 3, 1989||Dec 4, 1990||Minnesota Mining And Manufacturing Company||Light-sensitive silver halide photographic materials|
|US5215873 *||Apr 13, 1992||Jun 1, 1993||E. I. Du Pont De Nemours And Company||Process for developing silver halide recording materials|
|US5254448 *||Dec 23, 1991||Oct 19, 1993||Konica Corporation||Light-sensitive silver halide photographic material|
|US5468603 *||Nov 16, 1994||Nov 21, 1995||Minnesota Mining And Manufacturing Company||Photothermographic and thermographic elements for use in automated equipment|
|US5674671 *||Jun 27, 1995||Oct 7, 1997||Minnesota Mining And Manufacturing Company||Light senitive material having improved antistatic behavior|
|US5783380 *||Sep 24, 1996||Jul 21, 1998||Eastman Kodak Company||Thermally processable imaging element|
|US5804365 *||Mar 7, 1997||Sep 8, 1998||Eastman Kodak Company||Thermally processable imaging element having a crosslinked hydrophobic binder|
|US5888712 *||Dec 16, 1997||Mar 30, 1999||Eastman Kodak Company||Electrically-conductive overcoat for photographic elements|
|US5955250 *||Dec 16, 1997||Sep 21, 1999||Eastman Kodak Company||Electrically-conductive overcoat layer for photographic elements|
|US6071688 *||Jul 29, 1998||Jun 6, 2000||Eastman Kodak Company||Providing additives to a coating composition by vaporization|
|US7147909 *||Nov 30, 2004||Dec 12, 2006||Eastman Kodak Company||Electrophotographic media with carboxylic acid polymer|
|US7250202||Jun 18, 1999||Jul 31, 2007||Ilford Imaging Ch Gmbh||Recording sheets for ink jet printing|
|US7687136 *||Mar 30, 2010||Eastman Kodak Company||Fuser-oil sorbent electrophotographic toner receiver layer|
|US7754315 *||Jul 13, 2010||Eastman Kodak Company||Marking enhancement layer for toner receiver element|
|US20030141487 *||Dec 26, 2001||Jul 31, 2003||Eastman Kodak Company||Composition containing electronically conductive polymer particles|
|US20060115628 *||Nov 30, 2004||Jun 1, 2006||Eastman Kodak Company||Electrophotographic media with carboxylic acid polymer|
|US20060115629 *||Nov 30, 2004||Jun 1, 2006||Eastman Kodak Company||Fuser-oil sorbent electrophotographic toner receiver layer|
|US20060115631 *||Nov 30, 2004||Jun 1, 2006||Eastman Kodak Company||Marking enhancement layer for toner receiver element|
|US20060147658 *||Dec 16, 2005||Jul 6, 2006||Fuji Photo Film B.V.||Ink-jet recording medium|
|US20060159872 *||Dec 16, 2005||Jul 20, 2006||Fuji Photo Film B.V.||Ink-jet recording medium|
|US20060222787 *||Apr 3, 2006||Oct 5, 2006||Fuji Photo Film B.V.||Recording medium|
|US20060222788 *||Apr 3, 2006||Oct 5, 2006||Fuji Photo Film B.V.||Recording medium|
|US20120148768 *||Dec 2, 2011||Jun 14, 2012||Simpson Sharon M||Transparent ink-jet recording films, compositions, and methods|
|DE2900542A1 *||Jan 8, 1979||Jul 19, 1979||Konishiroku Photo Ind||Lichtempfindliches photographisches silberhalogenidmaterial|
|EP0112162A2||Dec 13, 1983||Jun 27, 1984||Konica Corporation||Light-sensitive silver halide photographic material|
|EP0429973A1 *||Nov 15, 1990||Jun 5, 1991||Du Pont De Nemours (Deutschland) Gmbh||Method for developing photographic silver halide recording materials|
|EP0697619A2||Aug 11, 1995||Feb 21, 1996||Eastman Kodak Company||High-contrast photographic elements with improved maximum density|
|WO1982001945A1 *||Oct 22, 1981||Jun 10, 1982||Kodak Co Eastman||Photographic antistatic compositions and elements coated therewith|
|WO1983002506A1 *||Dec 10, 1982||Jul 21, 1983||Kodak Compay Eastman||Electrically conductive compositions and use of same|
|U.S. Classification||430/635, 430/636, 430/950|
|International Classification||G03C1/85, G03C1/76|
|Cooperative Classification||G03C1/7614, G03C1/85, Y10S430/151|
|European Classification||G03C1/76D, G03C1/85|