US3884699A - Photographic materials having reduced static chargeability and method for their production - Google Patents

Photographic materials having reduced static chargeability and method for their production Download PDF

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US3884699A
US3884699A US380410A US38041073A US3884699A US 3884699 A US3884699 A US 3884699A US 380410 A US380410 A US 380410A US 38041073 A US38041073 A US 38041073A US 3884699 A US3884699 A US 3884699A
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fluorinated
group
surfactant
betaine
residue
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Elio Cavallo
Fulvio Furlan
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3M Co
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Minnesota Mining and Manufacturing Co
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/85Photosensitive materials characterised by the base or auxiliary layers characterised by antistatic additives or coatings

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  • ABSTRACT Primary Examiner-Norman G. Torchin Assistant ExaminerAlfonso T. Suro Pico Attorney, Agent, or FirmAlexander, Sell, Steldt & DeLaHunt [57] ABSTRACT The inclusion of both a substantially fluorinated surfactant and a non-fluorinated betaine and/or N-oxide surfactant into photographic layers and materials reduces the static chargeability of such materials.
  • the present invention relates to a method for reducing the chargeability of photographic layers and photographic elements, to photographic layers and photographic elements obtained with such a method.
  • a photographic material generally consists of a base, at least one layer of a silver halide emulsion dispersed in a hydrophilic colloidal binder and, possibly, of at least one protective layer for such an emulsion, essentially consisting of a hydrophilic colloidal binder.
  • a protective layer can be found either outside or inside such a photographic material (in this last case, for instance in color photographic materials, it is called interlayer).
  • a photographic material may include sub-layers, anti-halo layers and other auxiliary layers adjacent or not the emulsion layers.
  • a photographic material suitable for radiography particularly consists of a base, at least two emulsion layers each coated on one surface of said base and at least two protective layers for said emulsion layers. Such amaterial may also contain two sub-layers coated between the emulsion layers and the base.
  • emulsion layers and auxiliary layers such as for instance protective layers, interlayers, sublayers and anti-halo layers
  • auxiliary layers such as for instance protective layers, interlayers, sublayers and anti-halo layers
  • a radiographic material should be usable in angiographic tables (AOT) and in rapid machines wherein the film is conveyed at a high speed by means of rollers which exert thereon a strong pressure and friction action.
  • radiographic materials suitable for AOT must exhibit a rather high slipperiness index which reduces the dangers of the apparatus jamming.
  • the slipperiness index can be related to the static chargeability itself.
  • the chargeability of the layers is generally due to the fact that the layers essentially consist of gelatin or of another hydrophilic colloidal binder equivalent to gelatin which exhibits a low work function, i.e., a positive type chargeability.
  • a chargeability is generally modified by the presence of surfactants which induce a positive or a negative type chargeability into the layers according to their nature.
  • Non-fluorinated anionic surfactants of the type known to those skilled in the art generally induce a positive type chargeability into the layers.
  • Fluorinated anionic, non-ionic N-oxide or betaine surfactants induce a negative type chargeability into the same layers.
  • Betaine and/or N-oxide non-fluorinated surfactants in combination with nonfluorinated anionic surfactants do not substantially improve the static characteristics of the photographic layers, while on the contrary they improve slipperiness characteristics.
  • Fluorinated surfactants in combination with anionic non-fluorinated surfactants improve the static characteristics of the photographic layers only at a certain range of relative humidity and leave slipperiness characteristics unaltered.
  • the main scope of the present invention is that of providing a method for removing or at least reducing the electrostatic chargeability of the photographic layers and above all of the protective layers, the photographic material consists of.
  • a further scope of the present invention is that of providing photographic and radiographic materials having improved characteristics of electrostatic chargeability.
  • Another scope of the present invention is that of providing photographic and radiophotographic materials having improved characteristics of static chargeability ahd slipperiness.
  • fluorinated surfactants in combination with non-fluorinated betaine and/or N-oxide surfactants allows the chargeability of photographic layers to be reduced at all relative humidities for all of those photographic layers having a positive chargeability including chargeability due to the presence of nonfluorinated anionic surfactants.
  • Non-fluorinated anionic surfactants normally used in photography, for instance as coating, coagulant or dispersing agents, are surfactants of the type including hydrophobe group linked to an anionic hydrophilic group directly or by means of a bridge consisting of a divalent organic residue, as expressed by the following formula:
  • R is a non-fluorinated aliphatic, aromatic or a mixed hydrocarbon residue substituted or not substituted and preferably a linear or ramified alkyl group having from four to 18 carbon atoms or an aryl group substituted with one or more alkyl groups altogether having from four to 18 carbon atoms;
  • A is a chemical bond or a divalent organic residue, preferably a carbonyl, a sulphonyl, an amino or an alkylene group preferably having from one to three carbon atoms, an oxygen atom or groups consisting of two or more of the above-mentioned groups, such as for instance carbonylamino, sulphonylamino, aminocarbonyl, aminosulphonyl, ester or polyoxyalkylene groups preferably containing from two to forty oxyalkylene unities; and
  • X is an anionic group of the sulphonate, carboxylate
  • fluorinated surfactants we mean herewith any type of fluorinated surfactants capable of inducing a negative charge into the photographic layers containing them. They include preferably a hydrophobic portion R linked to a hydrophilic portion Y of every kind, may it be anionic, nonionic, cationic betaine or N-oxide, by means of a bridge A which represents a chemical bond or a divalent organic residue, as expressed by the formula:
  • R F is a substantially fluorinated hydrocarbon residue, preferably a fluorinated alkyl group having at least two carbon atoms and more preferably from two to 18 carbon atoms;
  • A is a chemical bond or a divalent organic residue
  • Y is a hydrophilic group of any type, may it be non ionic, anionic, cationic, betaine or N-oxide, and preferably a cationic group.
  • a substantially fluorinated hydrocarbon residue is by definition a fluorinated saturated monovalent nonaromatic radical of at least two carbon atoms.
  • the aliphatic chain may be straight, branched, or, if sufficiently large, cyclic and may include oxygen or trivalent nitrogen atoms bonded only to carbon atoms.
  • a fully fluorinated radical is preferred, but hydrogen or chlorine atoms may be present as substituents provided that not more than one atom of either is present for every two carbon atoms, and preferably, the radical contains at least a terminal perfluoromethyl group.
  • radicals containing a larger number of carbon atoms will function adequately, compounds containing not more than about 20 carbon atoms are preferred since larger radicals usually represent a less efficient utilization of fluorine than is possible with shorter chains. Fluoroaliphatic radicals containing about two to eight carbon atoms are most preferred.
  • Groups of this type are for instance a polyoxyalkylene group including from two to 40 oxyalkylene unities, wherein the alkylene group preferably has from one to three carbon atoms, a group of the sulphonate, carboxylate, sulphate or phosphate type, or an ammonium or phosphonium group, or a betaine group including a cation of the ammonium type and an anion of the carboxylate or sulphonate type, or a N-oxide group.
  • Groups of this type are, for instance:
  • R R and R are hydrogen or alkyl group having from one to 10, preferably from one to six carbon atoms, wherein said alkyl group possibly can be substituted for instance with an aryl group, preferably phenyl;
  • R and R or R R and R altogether also represent the non-metallic atoms necessary to form a heterocyclic quatemized nitrogen nucleus, such as for instance piridinium and imidazolinium',
  • D represents an anion such as for instance halide
  • B is an alkylene group possibly comprising a heterous bond, preferably having from one to six carbon atoms;
  • X is a carboxylate or sulphonate anion.
  • Fluorinated surfactants useful to the scope of the present invention are for instance described in U.S. Pat. Nos. 2,759,019; 2,764,602; 3,589,906; in the Belgian Pat. No. 739,245; and in the French Pat. No. 2,025,688.
  • R and A preferably represent groups of the abovedefined type
  • Z preferably represents a betaine group, such as for instance of the type comprising a cation of the ammonium type and an anion of the carboxylate and sulphonate type, such as for instance of the abovedescribed type or a group of the N-oxide type, as described above.
  • Betaine compounds of this type are for instance described in the U.S. Pat. No. 3,573,049 and N-oxide compounds of this type are for instance described in McCutcheons Detergents and Emulsifiers 1963 Annual (page 8).
  • the present invention concerns a method for reducing or removing the electrostatic chargeability of a photographic layer which consists of introducing at least a fluorinated surfactant, as defined above and at least a non-fluorinated betaine and/or N-oxide surfactant, as defined above, said layer preferably containing at least a non-fluorinated anionic surfactant.
  • the present invention particularly relates to a method for reducing or removing the electrostatic chargeability of a photographic layer which consists of introducing into said layer a cationic fluorinated surfactant, preferably comprising a partially or wholly fluorinated aliphatic hydrocarbon residue linked, by means of a chemical bond or a divalent organic residue comprising a carbonylamino or sulphonylamino group, with a chemical residue comprising an ammonium group, and at least a betaine or N-oxide nonfluorinated surfactant preferably a betaine comprising a non-fluorinated aliphatic hydrocarbon residue linked, by means of a divalent organic residue comprising a carbonylamino or sulphonylamino group, with a betaine residue, said layer containing an anionic nonfluorinated surfactant.
  • a cationic fluorinated surfactant preferably comprising a partially or wholly fluorinated aliphatic hydrocarbon residue linked, by means
  • the present invention relates to a photographic layer obtained with the above-described method and to a photographic element containing said layer.
  • the present invention further refers to an improved photographic material including:
  • said emulsion and/or said protective layer contains at least a fluorinated and a non-fluorinated betaine and/or N-oxide surfactant, as defined above.
  • the present invention particularly relates to a material of the above-described type containing the fluorinated and the non-fluorinated betaine and/or N-oxide surfactant at least in said protective layer for said emulsion layer.
  • the present invention relates to an improved radiographic material including:
  • the present invention particularly relates to a material of the above defined type containing at least a fluorinated cationic surfactant, at least a non-fluorinated betaine or N-oxide surfactant and at least a nonfluorinated anionic surfactant, said fluorinated cationic surfactant preferably comprising a partially or wholly fluorinated aliphatic hydrocarbon residue linked, by means of a chemical bond or a divalent organic residue comprising a carbonylamino or sulphonylamino group, with a chemical residue comprising an ammonium group; and said non-fluorinated betaine surfactant preferably comprising a non-fluorinated aliphatic hydrocarbon residue linked with a betaine residue by means of a divalent organic residue comprising a carbonyl-amino or sulphonylamino group.
  • compound no. 17 has been prepared in the following way:
  • propyl alcohol was added 0.2 mole of 25% methanolic Na 0 CH The mixture was digested at 60-70C for 1.5 h., then cooled and filtered. The
  • the photographic layers of the present invention comprise or essentially consist of hydrophilic colloidal binder.
  • a hydrophilic colloidal binder preferably is gelatin or any other film-forming binder permeable to the conventional processing baths for photographic materials alone or mixed with gelatin.
  • Such a hydrophilic binder can obtain, dispersed, hydrophobe polymer particles in order to improve the physical characteristics of the layers, thus obtained.
  • Particles of this type consist for instance of polyethylacrylate obtained for instance under the form of a latex.
  • Such layers can be hardened with hardeners known to those skilled in the art, such as for instance formaldehyde, glyoxale, succinaldehyde, glutaraldehyde, resorcinaldehyde, mucochloric acid, epoxides used alone or in association and can contain any other coating materials known to those skilled in the art.
  • hardeners known to those skilled in the art, such as for instance formaldehyde, glyoxale, succinaldehyde, glutaraldehyde, resorcinaldehyde, mucochloric acid, epoxides used alone or in association and can contain any other coating materials known to those skilled in the art.
  • the layers will contain, dispersed, silver halides, such as for instance bromide, iodide and chloride or mixtures thereof and antifog compounds and stabilizers in association therewith.
  • silver halides such as for instance bromide, iodide and chloride or mixtures thereof
  • antifog compounds and stabilizers in association therewith.
  • color emulsions such as layers can also contain couplers which upon color development with p-phenylene diamines give rise to yellow, magenta and cyan dyes.
  • Photographic layers of the above-mentioned type can contain anionic non-fluorinated surfactants preferably in a quantity ranging from 0.1 to 25, preferably from 1.5 to 5 g. per g. of gelatin or of another equivalent hydrophilic colloid.
  • the fluorinated and the nonfluorinated betaine or N-oxide surfactants are for instance added preferably in a quantity which respectively ranges from 0.1 to 25 and from 0.5 to 30 g. per 100 g. of gelatin or equivalent colloid, and more preferably in a quantity which respectively ranges from 0.1 to 5 and from 5 to 15 g. per 100 g. of gelatin.
  • the above-described surfactants can be both introduced into the photographic layers before being coated under the form of solutions, as known to those skilled in the art.
  • the solvents preferably used are water, alcohol and acetone or mixtures thereof or any other solvent, provided that it causes no damage to the photgraphic emulsion.
  • a ring of the material is stretched by several steel rollers and conveyed upon friction by a steel and gum roller.
  • the ring is started to move from a speed till to reach a given speed and the discharged immediately before the steel/gum roller couple by means of a 3M Type 210 electrostatic discharger.
  • the charge generated on the film by the passage between these two rollers is then measured.
  • the characteristics of the device and the measurement conditions are the following:
  • the charge density has been measured at a distance of cm. from the roller axis.
  • the slipperiness of the radiographic material in sheets has been measured by means of an ElemaSchonander device, wherein the sheet is placed between two intensifying screens, of the type known in radiography, on which a constant pressure is exerted.
  • the force necessary to pull out the film from the screens gives a slipperiness measure.
  • EXAMPLE 1 A silver bromo-iodide (98% bromide and 2% iodide) radiographic emulsion has been digested and added with the normal coating finals known in the photographic field (antifog agents, stabilizers, harderners, etc.). The emulsion, thus obtained, has been coated on both surfaces of a polyester base with the aid of anionic surfactants.
  • Two protective layers have then been coated on both emulsion layers: They consisted of gelatin and contained silica, as a matting agent, and the above-described Compound No. 8 and No. 2, as a coating surfactant, respectively in a quantity of 0.72 and 1.6 g. per 100 g. of gelatin. The same protective layers have been added or not with the surfactants of the present invention.
  • the quantities must be referred to 100 g. of gelatin in the protective layer.
  • EXAMPLE 5 The same material, as described above, added or not with Compounds No. 12 and 30 according to the present invention has been tested from the point of view of its antistatic characteristics with the above-described method. The results are shown in Table 5.
  • the quantities must be referred to 100 g. of gelatin in the protective layer.
  • a method for reducing the chargeability of photographic layers, upon a support, which essentially consist of a hydrophylic colloidal binder comprising gelatin said method consisting of introducing at least one surfactant having a substantially fluorinated cation or anion bonded to a hydrophilic group and at least one of a nonfluorinated betaine orN-oxide surfactant into said layers by mixing the hydrophilic colloidal binder and surfactants prior to formation of the photographic layer containing the surfactants.
  • fluorinated surfactant is a surfactant having a substantially fluorinated cation.
  • At least one layer of a silver halide emulsion dispersed in a hydrophylic colloidal binder which consists of introducing at least one surfactant having a substantially fluorinated anion or cation and at least a non-fluorinated betaine and/or N-oxide surfactant into the said at least one emulsion layer by mixing the surfactants and binder prior to formation of the layer containing the surfactants.
  • a photographic layer on a support, essentially consisting of a hydrophilic colloidal binder comprising gelatin characterized in that it contains at least one surfactant having a substantially fluorinated cation or anion and at least a non-fluorinated betaine and/or N- oxide surfactant.
  • a photographic layer on a support the layer essentially consisting of a hydrophylic colloidal binder comprising gelatin, characterized in that it contains at least one surfactant having a substantially fluorinated anion or cation, at least one selected from the group of nonfluorinated betaine and N-oxide surfactants, and at least one non-fluorinated anionic surfactant.
  • R represents a substantially fluorinated hydrocarbon residue
  • A is a chemical bond or a divalent organic residue
  • R is a fluorinated alkyl group having from two to eight carbon atoms
  • A is a chemical bond or a divalent organic residue comprising at least a carbonyl, sulphonylamino, alkylene residue having from one to three carbon atoms, oxygen, carbonylamino, 'sulphonylamino, aminocarbonyl, aminosulphonyl, ester, polyoxyalkylene having from two to 40 oxyalkylene unities and/or
  • R is an alkyl group having from four to 18 carbon atoms and Z is a betaine hydrophylic group comprising an ammonium group and (an anionic group or a group comprising an N-oxide bond.
  • a photographic element comprising at least a base and a photographic layer according to any ofclaim 5.
  • a photographic element including:
  • said protective layers contain at least one surfactant having a substantially fluorinated anion or cation and at least a nonfluorinated betaine and/or N-oxide surfactant.
  • the photographic element of claim 13 characterized in that it contains said fluorinated cationic surfactant comprising a partially or wholly fluorinated aliphatic hydrocarbon residue linked, by means of a chemical bond or a divalent organic residue comprising a carbonylamino or sulphonylamino group, with a chemical residue comprising an ammonium group; and at least a non-fluorinated betaine surfactant comprising a non-fluorinated aliphatic hydrocarbon residue linked with a betaine residu'e by means of a divalent organic residue comprising a carbonylamino or a sulphonylamino group.
  • A is a chemical bond or a divalent residue at least comprising a carbonyl, sulphonyl, amino, alkylene residue having from one to three carbon atoms, oxygen, carbonylamino, sulphonylamino,
  • the photographic material further comprises at least one protective layer comprising gelatin for said emulsion layer, and where said surfactants are present in at least one of said emulsion and'protective layers.
  • the emulsion layer further contains at least one non-fluorinated anionic surfactant.
  • the photographic layer of claim 6 characterized in that it contains a non-fluorinated anionic surfactant; at least a fluorinated cationic surfactant comprising a partially or wholly fluorinated aliphatic hydrocarbon residue linked, by means of a chemical bond or a divalent organic residue comprising a carbonylamino or a sulphonylamino group, with a chemical residue comprising an ammonium group; and at least a nonfluorinated betaine residue comprising a nonfluorinated aliphatic hydrocarbon residue linked with a betaine residue by means of a divalent organic residue comprising a carbonylamino or a sulphonylamino group.
  • R represents a substantially fluorinated hydrocarbon residue
  • A is a chemical bond or a divalent organic residue
  • Y represents an anionic, non-ionic, or cationic betaine or N-oxide hydrophylic group.
  • Y represents an anionic, non-ionic, or cationic betaine or N-oxide hydrophylic group.
  • R is a non-fluorinated hydrocarbon residue
  • A is a chemical bond or a divalent organic residue
  • Y Z represents a betaine or N-oxide hydrophilic group.
  • R is a non-fluorinated hydrocarbon residue
  • A is a chemical bond or a divalent organic residue
  • R is a fluorinated alkyl group having from two to eight carbon atoms
  • A is a chemical bond or a divalent organic residue comprising at least a carbonyl, sulphonylamino, alkylene residue having from one to three carbon atoms, oxygen, carbonylamino, sulphonylamino, aminocarbonyl, aminosulphonyl, ester, polyoxyalkylene having from two to 40 oxyalkylene unities and/or R is an alkyl group having from four to 18 carbon atoms and Z is a betaine hydrophylic group comprising an ammonium group and/or an anionic group or a group comprising an N-oxide bond.
  • a photographic element comprising at least a base and a photographic layer according to claim 6.
  • R F represents a partially or wholly fluorinated hydrocarbon residue
  • A represents a chemical bond or a divalent organic residue
  • Y represents a hydrophylic anionic, non-ionic, meationic betaine or N-oxide group
  • the non-fluorinated betaine and/0r N-oxide surfactant corresponds to the formula:
  • R represents a non-fluorinated hydrocarbon residue
  • A has the same meaning as said above;
  • Z represents a hydrophylic betaine or N-oxide group.
  • R is an alkyl group having from two to eight carbon atoms
  • A is a chemical bond or a divalent residue at least comprising a carbonyl, sulphonyl, amino, alkylene residue having from one to three carbon atoms, oxygen, carbonylamino, sulphonylamino, aminocarbonyl, ester, polyoxyalkylene having from two to 40 oxyalkylene unities and/or
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IT51726/72A IT966734B (it) 1972-07-24 1972-07-24 Metodo per ridurre la caricabilita statica di strati fotografici e di elementi fotografici strati fotografici ed elementi fotografici ottenuti con tale metodo

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Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4050940A (en) * 1975-03-15 1977-09-27 Konishiroku Photo Industry Co., Ltd. Process for the preparation of a photographic material
US4175969A (en) * 1978-03-17 1979-11-27 Gaf Corporation Antistatic photographic X-ray film having a uniform protective surface coating of surfactant oligomer of tetrafluoroethylene
FR2426038A1 (fr) * 1978-05-15 1979-12-14 Minnesota Mining & Mfg Nouveaux derives d'isopropylbenzene et procede de leur preparation
US4229524A (en) * 1978-06-02 1980-10-21 Fuji Photo Film Co., Ltd. Photographic light sensitive material with antistatic property
US4267265A (en) * 1974-02-13 1981-05-12 Fuji Photo Film Co., Ltd. Photographic light-sensitive material
US4272615A (en) * 1978-07-03 1981-06-09 Fuji Photo Film Co., Ltd. Photographic light-sensitive antistatic containing material
WO1982001945A1 (en) * 1980-11-24 1982-06-10 Kodak Co Eastman Photographic antistatic compositions and elements coated therewith
US4385110A (en) * 1975-05-02 1983-05-24 Fuji Photo Film Co., Ltd. Process for preparing color photographic light-sensitive materials
US4806571A (en) * 1988-05-06 1989-02-21 The Dow Chemical Company Organic composition containing a fluoroalkyl sulfonic acid salt
US4822724A (en) * 1986-12-18 1989-04-18 Minnesota Mining And Manufacturing Company Process for the formation of stable color photographic images
US4975363A (en) * 1988-11-25 1990-12-04 Minnesota Mining And Manufacturing Company Light-sensitive silver halide photographic materials
US5098821A (en) * 1987-07-24 1992-03-24 Minnesota Mining And Manufacturing Company Light-sensitive silver halide photo-graphic materials
US5300394A (en) * 1992-12-16 1994-04-05 Eastman Kodak Company Dispersions for imaging systems
US5411844A (en) * 1994-03-31 1995-05-02 Eastman Kodak Company Photographic element and coating composition therefor
US5418128A (en) * 1994-03-31 1995-05-23 Eastman Kodak Company Photographic element and coating composition therefor
US5576074A (en) * 1995-08-23 1996-11-19 Minnesota Mining And Manufacturing Company Laser write process for making a conductive metal circuit
US5674671A (en) * 1994-07-18 1997-10-07 Minnesota Mining And Manufacturing Company Light senitive material having improved antistatic behavior
US5744295A (en) * 1993-09-24 1998-04-28 Eastman Kodak Company Antistatic composition containing anionic and cationic surface active agents wherein both surface active agents comprises polyoxyalkylene groups
US6171707B1 (en) * 1994-01-18 2001-01-09 3M Innovative Properties Company Polymeric film base having a coating layer of organic solvent based polymer with a fluorinated antistatic agent
US6699648B2 (en) 2002-03-27 2004-03-02 Eastman Kodak Company Modified antistatic compositions and thermally developable materials containing same
US6762013B2 (en) 2002-10-04 2004-07-13 Eastman Kodak Company Thermally developable materials containing fluorochemical conductive layers
CN102489216A (zh) * 2011-12-06 2012-06-13 华中师范大学 两性含氟离子型表面活性剂的制备方法与应用

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5479366A (en) * 1977-12-07 1979-06-25 Patsukusu Kk Lubricant for record disc* magnetic tape and photographic film
JPS58200235A (ja) * 1982-05-18 1983-11-21 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料
GB2299680B (en) * 1995-04-05 1998-10-28 Kodak Ltd Photographic material

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2420611A (en) * 1945-12-14 1947-05-13 Gen Aniline & Film Corp Antistatic photographic film
US3775126A (en) * 1972-02-29 1973-11-27 Eastman Kodak Co Light-sensitive element comprising a coating layer containing a mixture of a cationic perfluorinated alkyl and an alkylphenoxypoly(propylene oxide)

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US366478A (en) * 1887-07-12 Bake-pan
DE1547721A1 (de) * 1965-08-16 1969-12-18 Eastman Kodak Co Verwendung von Sulfobetainen als Beschichtungshilfsmittel bei der Herstellung photographischer Schichten
US3489567A (en) * 1967-03-03 1970-01-13 Eastman Kodak Co Lubricating compositions and photographic elements having lubricated surface
US3573049A (en) * 1967-10-02 1971-03-30 Eastman Kodak Co Photographic materials and processes for developing photographic compositions having a zwitterionic and anionic elements
US3589906A (en) * 1968-10-16 1971-06-29 Du Pont Photographic layers containing perfluoro compounds and coating thereof
GB1293189A (en) * 1970-06-04 1972-10-18 Agfa Gevaert Photographic silver halide element
BE789556A (fr) * 1971-10-01 1973-03-29 Union Carbide Corp Element alcain de pile au zinc
JPS48101118A (es) * 1972-02-29 1973-12-20

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2420611A (en) * 1945-12-14 1947-05-13 Gen Aniline & Film Corp Antistatic photographic film
US3775126A (en) * 1972-02-29 1973-11-27 Eastman Kodak Co Light-sensitive element comprising a coating layer containing a mixture of a cationic perfluorinated alkyl and an alkylphenoxypoly(propylene oxide)

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4267265A (en) * 1974-02-13 1981-05-12 Fuji Photo Film Co., Ltd. Photographic light-sensitive material
US4050940A (en) * 1975-03-15 1977-09-27 Konishiroku Photo Industry Co., Ltd. Process for the preparation of a photographic material
US4385110A (en) * 1975-05-02 1983-05-24 Fuji Photo Film Co., Ltd. Process for preparing color photographic light-sensitive materials
US4175969A (en) * 1978-03-17 1979-11-27 Gaf Corporation Antistatic photographic X-ray film having a uniform protective surface coating of surfactant oligomer of tetrafluoroethylene
US4328280A (en) * 1978-05-15 1982-05-04 Minnesota Mining And Manufacturing Company Suppression of spark discharges from negatively triboelectrically charged surfaces
FR2426038A1 (fr) * 1978-05-15 1979-12-14 Minnesota Mining & Mfg Nouveaux derives d'isopropylbenzene et procede de leur preparation
US4229524A (en) * 1978-06-02 1980-10-21 Fuji Photo Film Co., Ltd. Photographic light sensitive material with antistatic property
US4272615A (en) * 1978-07-03 1981-06-09 Fuji Photo Film Co., Ltd. Photographic light-sensitive antistatic containing material
WO1982001945A1 (en) * 1980-11-24 1982-06-10 Kodak Co Eastman Photographic antistatic compositions and elements coated therewith
US4335201A (en) * 1980-11-24 1982-06-15 Eastman Kodak Company Antistatic compositions and elements containing same
US4822724A (en) * 1986-12-18 1989-04-18 Minnesota Mining And Manufacturing Company Process for the formation of stable color photographic images
US5098821A (en) * 1987-07-24 1992-03-24 Minnesota Mining And Manufacturing Company Light-sensitive silver halide photo-graphic materials
US4806571A (en) * 1988-05-06 1989-02-21 The Dow Chemical Company Organic composition containing a fluoroalkyl sulfonic acid salt
US4975363A (en) * 1988-11-25 1990-12-04 Minnesota Mining And Manufacturing Company Light-sensitive silver halide photographic materials
US5300394A (en) * 1992-12-16 1994-04-05 Eastman Kodak Company Dispersions for imaging systems
US5744295A (en) * 1993-09-24 1998-04-28 Eastman Kodak Company Antistatic composition containing anionic and cationic surface active agents wherein both surface active agents comprises polyoxyalkylene groups
US6171707B1 (en) * 1994-01-18 2001-01-09 3M Innovative Properties Company Polymeric film base having a coating layer of organic solvent based polymer with a fluorinated antistatic agent
US5411844A (en) * 1994-03-31 1995-05-02 Eastman Kodak Company Photographic element and coating composition therefor
US5418128A (en) * 1994-03-31 1995-05-23 Eastman Kodak Company Photographic element and coating composition therefor
US5674671A (en) * 1994-07-18 1997-10-07 Minnesota Mining And Manufacturing Company Light senitive material having improved antistatic behavior
US5576074A (en) * 1995-08-23 1996-11-19 Minnesota Mining And Manufacturing Company Laser write process for making a conductive metal circuit
US6699648B2 (en) 2002-03-27 2004-03-02 Eastman Kodak Company Modified antistatic compositions and thermally developable materials containing same
US20040126718A1 (en) * 2002-03-27 2004-07-01 Kumars Sakizadeh Modified antistatic compositions and thermally developable materials containing same
US6762013B2 (en) 2002-10-04 2004-07-13 Eastman Kodak Company Thermally developable materials containing fluorochemical conductive layers
CN102489216A (zh) * 2011-12-06 2012-06-13 华中师范大学 两性含氟离子型表面活性剂的制备方法与应用
CN102489216B (zh) * 2011-12-06 2014-01-22 华中师范大学 两性含氟离子型表面活性剂的制备方法与应用

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GB1445407A (en) 1976-08-11
CA1012820A (en) 1977-06-28
JPS5239291B2 (es) 1977-10-04
DE2337638A1 (de) 1974-02-21
FR2193993A1 (es) 1974-02-22
IT966734B (it) 1974-02-20
JPS49133023A (es) 1974-12-20
BE802671A (fr) 1974-01-23
AR200731A1 (es) 1974-12-13
FR2193993B1 (es) 1979-08-03
DE2337638C2 (de) 1983-11-03

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