EP0675402B1 - Schutzschicht und diese enthaltende photographische Materialien - Google Patents

Schutzschicht und diese enthaltende photographische Materialien Download PDF

Info

Publication number
EP0675402B1
EP0675402B1 EP19950420077 EP95420077A EP0675402B1 EP 0675402 B1 EP0675402 B1 EP 0675402B1 EP 19950420077 EP19950420077 EP 19950420077 EP 95420077 A EP95420077 A EP 95420077A EP 0675402 B1 EP0675402 B1 EP 0675402B1
Authority
EP
European Patent Office
Prior art keywords
photographic material
terpolymer
protective layer
material according
groups
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP19950420077
Other languages
English (en)
French (fr)
Other versions
EP0675402A1 (de
Inventor
Francois Jean-Marie C/O Kodak-Pathe Bredoux
Gérard Maurice c/o Kodak-Pathe Droin
Yannick C/O Kodak-Pathe Begel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kodak Pathe SA
Eastman Kodak Co
Original Assignee
Kodak Pathe SA
Eastman Kodak Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kodak Pathe SA, Eastman Kodak Co filed Critical Kodak Pathe SA
Publication of EP0675402A1 publication Critical patent/EP0675402A1/de
Application granted granted Critical
Publication of EP0675402B1 publication Critical patent/EP0675402B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/3029—Materials characterised by a specific arrangement of layers, e.g. unit layers, or layers having a specific function
    • 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
    • G03C1/7614—Cover layers; Backing layers; Base or auxiliary layers characterised by means for lubricating, for rendering anti-abrasive or for preventing adhesion

Definitions

  • the present invention concerns a photographic material comprising, in addition to the conventional light-sensitive silver halide layers, a protective top layer. More particularly, the invention concerns a photographic material comprising a protective top layer which prevents marks from appearing during photographic processing.
  • top layers are useful, for example, for protecting the photographic materials from fingermarks, abrasion or scratches which appear either during the preparation of the photographic materials or during photographic processing.
  • These protective top layers may also provide a special surface texture such as matt surfaces, or they may be used as an anti-reflective layer.
  • top layers may be temporary or permanent layers.
  • Such layers are obtained by applying to a photographic material a coating of solutions or dispersions with particular compositions.
  • a coating of solutions or dispersions with particular compositions for example, US patent 2 536 764 describes a top layer containing transparent solid particles with sizes smaller than one micrometre.
  • the patent application WO 91/18325 describes a photographic material comprising a protective layer consisting of (a) a hydroxylated latex, (b) a hydrolysed metal alkoxide and (c) a polyfluoroalkylether surfactant.
  • a protective layer consisting of (a) a hydroxylated latex, (b) a hydrolysed metal alkoxide and (c) a polyfluoroalkylether surfactant.
  • European patent application 245 090 concerns a photographic material comprising a top layer consisting of a fluorinated compound and/or an anionic surfactant and a hardener with a high molecular weight. Such a top layer has antistatic properties.
  • these top layers must be completely transparent and flexible. Their components must not dissolve in photographic baths during photographic processing. In addition, these protective layers must not delay the kinetics of development.
  • the present invention concerns a novel protective layer which enables the problems of marks during photographic processing to be totally eliminated, but without altering the sensitometric properties.
  • the invention concerns a photographic material comprising a support covered with at least one light sensitive silver halide emulsion layer and a protective layer covering the emulsion layer.
  • the protective layer comprises a hydrophilic collo ⁇ dal binder containing, in combination, a surface-active fluorinated polyether and a vinyl polymer obtained from monomers as recited in Claim 1.
  • R 3 is preferably hydrogen or an alkyl group having from 1 to 4 carbon atoms.
  • R 2 and R 1 preferably comprise from 1 to 4 carbon atoms.
  • the vinyl polymer is a vinyl terpolymer consisting of : in which R 3 and X are such as defined above, x represents between 10% and 95% and preferably between 85% and 95% by weight of terpolymer, y represents between 3% and 50% and preferably between 5% and 10% by weight of terpolymer and z represents between 2% and 80% and preferably between 4% and 10% by weight of terpolymer, provided that the sum of x, y and z is 100%.
  • the preferred terpolymer according to the invention is the terpolymer in which x represents 88%, y represents 7% and z represents 5%.
  • the surface-active fluorinated polyethers are surfactants which contain an aliphatic moiety having from 3 to 16 carbon atoms at least partially substituted by fluorine atoms, and optionally aliphatic moieties having from 3 to 16 carbon atoms not substituted by fluorine.
  • the polyether moiety preferably comprises at least 3 ether functions, more preferably from 9 to 14 ether functions.
  • the polyether moiety may contain alkylene chains such as polyethylene or polypropylene chains.
  • the surface-active fluorinated polyethers are compounds or a mixture of compounds of the formula : in which R is a hydrogen atom or an alkyl group, for example methyl.
  • a surfactant corresponding to this definition is Zonyl-FSN® manufactured by DuPont.
  • the quantity of surfactant which is used in the protective layer of the present invention is between 0.2 and 5.0 mg/dm 2 , preferably 0.8 to 2.0 mg/dm 2 .
  • the quantity of vinyl terpolymer which is used in the protective layer of the present invention is between 0.5 and 10 mg/dm 2 , preferably between 1 and 5 mg/dm 2 .
  • a fine grain silver halide emulsion which does not participate in the formation of the image is introduced into the protective layer.
  • This emulsion has been described in detail in the patent application WO 93/19397.
  • This emulsion is preferably a silver bromochloride fine-grain emulsion containing 50% molar silver bromide.
  • the protective layer can contain other compounds useful in photography.
  • the protective layer of the invention may be used on any type of colour or black and white photographic material, such as negative, positive or reversible materials.
  • the colour photographic materials generally comprise a support carrying at least one blue-sensitive silver halide emulsion layer with which is associated a yellow dye forming coupler, at least one green-sensitive silver halide emulsion layer with which is associated a magenta dye forming coupler, and at least one red-sensitive silver halide emulsion layer with which is associated a cyan dye forming coupler.
  • the support may be any appropriate support used for photographic materials.
  • Conventional supports include polymer films, paper (including paper coated with polymer), glass and metal. Research Disclosure , December 1978, No 17643, Section XVII, provides details concerning supports and auxiliary layers for photographic materials.
  • Silver halide emulsions may be chemically sensitised according to the methods described in Section III of the Research Disclosure referred to above.
  • the chemical sensitisers generally used are sulphur and/or selenium and gold compounds. Sensitisation by reduction can also be used.
  • the halide grains may have different compositions. It is possible for example to use silver bromide, silver iodobromide, silver chloride, silver chloroiodide or silver chlorobromoiodide grains.
  • the silver halide grains may be spherical, cubic, octahedral, cubo-octahedral or tabular.
  • the silver halide grains may be core/shell grains, for example as in US patent 3 505 068, or may have epitaxial deposits as in US patent 4 713 320.
  • These silver halide emulsions may also contain doping agents, such as rhodium, indium, osmium, iridium, etc ions, generally in small quantities.
  • the silver halide emulsions and other layers for photographic materials of this invention may contain, as a carrier, hydrophilic colloids, used alone or in combination with other polymer substances (for example latexes).
  • hydrophilic colloids comprise both natural substances such as cellulose derivatives - for example cellulose esters, proteins or protein derivatives, gelatin, gelatin treated with a base (bone gelatin or tanned gelatin) or gelatin treated with an acid (pigskin gelatin), gelatin derivatives, for example acetylated gelatin, phthalated gelatin etc, or polysaccharides such as dextran, gum arabic, zein, casein, pectin, collagen derivatives, collodion, agar-agar and albumin.
  • the emulsions may be polydisperse or monodisperse, or may consist of a mixture of emulsions having different grain sizes and/or compositions.
  • the spectral sensitisation, or chromatisation, methods are described in the same publication, Section IV.
  • the sensitising dyes may be added at various stages in the preparation of the emulsion, particularly before, during or after chemical sensitisation.
  • the silver halide emulsions may be spectrally sensitised with dyes from various classes, including the class of polymethine dyes, which comprises cyanines, merocyanines, complex cyanines and merocyanines (ie tri-, tetra- and polynuclear cyanines and merocyanines), oxonols, hemioxonols, styryls, merostyryls and streptocyanines.
  • polymethine dyes which comprises cyanines, merocyanines, complex cyanines and merocyanines (ie tri-, tetra- and polynuclear cyanines and merocyanines), oxonols, hemioxonols, styryls, merostyryls and streptocyanines.
  • polymethine dyes which comprises cyanines, merocyanines, complex cyanines and merocyanines (ie tri-
  • the photographic materials of the invention may contain, inter alia, optical brighteners, anti-fogging compounds, surfactants, plasticisers, lubricants, hardeners, stabilisers, and absorption and/or diffusion agents as described in Sections V, VI, VIII, XI, XII and XVI of the Research Disclosure cited above.
  • the photographic materials after being exposed, undergo a photographic process comprising a silver development of the latent image (black and white development), and a chromogenic development in the presence of a chromogenic developer and a coupler, which in certain cases may be incorporated into the photographic material.
  • the photographic materials are then washed and subjected to a bleaching and then a fixing bath, before being processed in a stabilising bath.
  • the bleaching and fixing baths may be replaced by a single bleach/fixing bath.
  • the silver development is carried out in the presence of a reducing compound which enables the exposed silver halide grains to be transformed into metal silver grains.
  • a reducing compound which enables the exposed silver halide grains to be transformed into metal silver grains.
  • These compounds are chosen from the dihydroxybenzenes such as hydroquinone, the 3-pyrazolidones, the aminophenols, etc. These compounds may be used alone or in a mixture.
  • This first bath may, in addition, contain a stabiliser such as sulphites, a buffer such as carbonates, boric acid, borates or alkanolamines.
  • the chromogenic developer contained in the chromogenic development bath which enables the colour image to be obtained is generally an aromatic primary amine such as the p-phenylenediamines, and more particularly the N,N-dialkyl-p-phenylenediamines, where the alkyl radicals and the aromatic nucleus may be substituted or not.
  • the p-phenylenediamines used as chromogenic developers are for example N,N-diethyl-p-phenylenediamine monochlorhydrate, 4-N,N-dimethyl-2-methylphenylenediamine monochlorhydrate, or 4-(N-ethyl-N-2-hydroxyethyl)-2-methylphenylenediamine sulphate.
  • This chromogenic developing bath may contain other compounds such as stabilisers, development accelerators, which are generally pyridinium compounds, or other compounds.
  • the essential compound of the bleaching bath is an oxidising compound which transforms the metal silver into silver ions such as, for example, the alkaline metal salts of a ferric complex of an aminocarboxylic acid, or persulphate compounds.
  • the bleaching compounds commonly used are ferric complexes of nitrolotriacetic acid, ethylenediamine tetracetic acid, 1,3-propylenediamine tetracetic acid, triethylenetriamine pentacetic acid, orthodiaminocyclohexane tetracetic acid, ethyliminodiacetic acid, etc.
  • the fixing bath enables the silver halide to be completely transformed into a soluble silver complex which is then eliminated from the layers of the photographic material.
  • the compounds used for fixing are, for example, thiosulphates such as ammonium thiosulphates or alkaline metal thiosulphates. Stabilisers or sequestering agents may be added to the fixing bath.
  • the processing generally comprises a stabilising bath containing a colour stabiliser such as formaldehyde, and a wetting agent.
  • a colour stabiliser such as formaldehyde
  • the photographic materials of the invention are reversal materials as described in the patent application WO 93/19397.
  • the reversal materials undergo photographic processing comprising, after the silver development step, a reversal step which consists of making the unexposed residual silver halide grains developable by means of a fogging exposure or a chemical fogging and subjecting these fogged silver halide grains to a chromogenic development in the presence of a chromogenic developer and a coupler, the latter generally being incorporated in the material.
  • the photographic material is a colour reversal material which is exposed and then processed according to the standard method of Ektachrome® R-3 process.
  • the photographic material used in the following example is the Ektachrome® photographic material of the Radiance® type to which has been applied a protective layer comprising gelatin and a fine grain silver bromochloride emulsion (50% bromide) which does not participate in the formation of the image with an average equivalent spherical diameter of 0.11 ⁇ m, and in a proportion of 0.15 mg/dm 2 .
  • the photographic material has been hardened by means of a quantity of hardener of around 0.9% by weight of total gelatin introduced into one of the light-sensitive photographic layers.
  • the material thus obtained is exposed to the light of a tungsten lamp (2850° K). It is then processed in a processing machine comprising conventional Ektachrome® R-3 process.
  • the standard Ektachrome® R-3 process comprises the following stages : Black and white development 1 min 15 sec Washing 1 min 30 sec Re-exposure Chromogenic development (38°C) 2 min 15 sec Washing 0 min 45 sec Bleaching/fixing 2 min Washing 2 min 15 sec
  • a protective layer as defined in Example 1 and containing in addition the vinyl terpolymer (PI), is applied to the Radiance® photographic material.
  • a protective layer with a vinyl terpolymer content of 1 mg/dm 2 is thus obtained.
  • the photographic material obtained is then processed according to the process described in Example 1. in which x represents 88% by weight of terpolymer, y represents 7% by weight of terpolymer and z represents 5% by weight of terpolymer.
  • An aqueous coating composition of Example 2 is applied to the photographic material of Example 1, modifying the vinyl terpolymer (PI) quantity in order to obtain a protective layer with a terpolymer content of 2 mg/dm 2 .
  • PI vinyl terpolymer
  • the photographic material obtained is then processed according to the process described in Example 1.
  • a protective layer is thus obtained with a Zonyl-FSN® surfactant content of 1 mg/dm 2 and a copolymer content of 1 mg/dm 2 .
  • the photographic material obtained is then processed according to the process described in Example 1.
  • the protective layer of Example 4 is reproduced and the hardener content is increased from 0.9 to 1.3% by weight of total gelatin, this hardener being introduced into one of the light-sensitive photographic layers.
  • the photographic material obtained is then processed according to the process described in Example 1.
  • Examples 1 to 5 are assembled in the table below.
  • the number of "M” represents the mark level which appears during photographic processing and the number of "S” represents the magnitude of the impurities which appear on the surface of the processing baths after developing each photographic material described above.
  • the comparative Examples 2 and 3 show that the presence of the vinyl polymer used in the invention in the protective layer reduces the appearance of marks during processing. However, with such a terpolymer, the brillance of the paper is affected. In addition, the polymer dissolves in the processing baths, which causes the baths to become contaminated very rapidly.
  • Examples 4 and 5 show that the use of the vinyl polymer in combination with the fluorinated polyether in the protective layer enables the marks due to processing to be completely eliminated. Moreover, the development kinetics remains comparable to that obtained with the photographic material of Example 1 and no impairment of the sensitometric properties is observed. In particular the speed of the photographic material is not impaired.
  • Examples 4 and 5 in the above table show that the tanning level has no influence on the appearance of marks during processing, in the presence of the protective layer used in the invention.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)

Claims (8)

  1. Fotografisches Material mit einem Träger, mindestens einer Licht-empfindlichen Silberhalogenid-Emulsionsschicht und einer Schutzschicht, wobei die Schmutzschicht ein hydrophiles, kolloidales Bindemittel aufweist mit mindestens einem oberflächenaktiven, fluoroalkylierten Polyether und mindestens einem Vinylterpolymer, erhalten aus den Monomeren (A), (B) und (C) der Formeln: (A)   (R3)2C = CR3 - COOR1 (B)   (R3)2C = CR3 - COOR2OCOR2COR1 (C)   (R3)2C = CR3 - CONR3R2SO3 ⊖ X worin die Gruppen R1, die gleich oder verschieden sein können, Alkyl-Reste mit einer geraden oder verzweigten Kette mit 1 bis 12 Kohlenstoffatomen sind; die Gruppen R2, die gleich oder verschieden sein können, Alkylengruppen mit einer geraden oder verzweigten Kette mit 1 bis 10 Kohlenstoffatomen sind; die Gruppe R3 ein Wasserstoffatom ist oder eine Alkylgruppe mit einer geraden oder verzweigten Kette mit 1 bis 5 Kohlenstoffatomen, und X das Kation ist, das der Sulfogruppe zugeordnet ist, ausgewählt aus Alkalimetallionen, Ammonium- oder Alkylammonium-Gruppen.
  2. Fotografisches Material nach Anspruch 1, in dem der oberflächenaktive, fluoroalkylierte Polyether durch die Formel definiert ist:
    Figure 00150001
    worin R für ein Wasserstoffatom oder eine Methylgruppe steht.
  3. Fotografisches Material nach Anspruch 2, in dem der oberflächenaktive, fluoroalkylierte Polyether Zonyl-FSN® ist.
  4. Fotografisches Material nach Anspruch 1, in dem das Vinylpolymer ein Vinylterpolymer ist, bestehend aus:
    Figure 00160001
    worin die Gruppen R3, gleich oder verschieden, Wasserstoffatome sind, Alkyl-Reste mit einer geraden oder verzweigten Kette mit 1 bis 5 Kohlenstoffatomen, und worin X das Kation ist, das der Sulfogruppe zugeordnet ist, ausgewählt aus Alkalimetallionen, Ammonium- oder Alkylammonium-Gruppen, und worin
       x darstellt zwischen 10 und 95 Gew.-% und vorzugsweise zwischen 85 und 95 Gew.-% des Terpolymeren, y darstellt zwischen 3 und 50 Gew.-% und vorzugsweise zwischen 5 und 10 Gew.-% des Terpolymeren, und z darstellt zwischen 2 und 80 Gew.-% und vorzugsweise zwischen 4 und 10 Gew.-% des Terpolymeren, wobei gilt, daß die Summe von x, y und z gleich 100 % ist.
  5. Fotografisches Material nach Anspruch 4, in dem das Vinylterpolymer ein solches ist, das x 88 % ausmacht, y 7 % ausmacht und z 5 % ausmacht.
  6. Fotografisches Material nach Anspruch 5, in dem der Terpolymer-Gehalt in der Schutzschicht zwischen 0,5 und 10 mg/dm2, und vorzugsweise zwischen 1 und 5 mg/dm2, liegt.
  7. Fotografisches Material nach Anspruch 1, in dem der Gehalt an oberflächenaktivem, fluoroalkyliertem Polyether in der Schutzschicht zwischen 0,2 und 5 mg/dm2, und vorzugsweise zwischen 1 und 2 mg/dm2, liegt.
  8. Fotografisches Material nach einem der vorstehenden Ansprüche, in dem die Schutzschicht ferner eine feinkörnige Silberbromochlorid-Emulsion enthält, die nicht an der Formation des Bildes beteiligt ist, wobei die Silberbromochlorid-Körner einen Bromidgehalt von etwa 50 Mol-% und eine mittlere Größe unterhalb 0,5 µm aufweisen.
EP19950420077 1994-03-31 1995-03-27 Schutzschicht und diese enthaltende photographische Materialien Expired - Lifetime EP0675402B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9404266 1994-03-31
FR9404266A FR2718257B1 (fr) 1994-03-31 1994-03-31 Surcouche protectrice et produits photographiques comprenant cette surcouche.

Publications (2)

Publication Number Publication Date
EP0675402A1 EP0675402A1 (de) 1995-10-04
EP0675402B1 true EP0675402B1 (de) 2000-08-09

Family

ID=9461963

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19950420077 Expired - Lifetime EP0675402B1 (de) 1994-03-31 1995-03-27 Schutzschicht und diese enthaltende photographische Materialien

Country Status (4)

Country Link
EP (1) EP0675402B1 (de)
JP (1) JPH07319112A (de)
DE (1) DE69518268T2 (de)
FR (1) FR2718257B1 (de)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1466600A (en) * 1965-12-20 1977-03-09 Eastman Kodak Co Copolymer-containing layers useful in photogrpahy and coating compositions for their manufacture
EP0245090A3 (de) * 1986-05-06 1990-03-14 Konica Corporation Photographisches Silberhalogenid mit antistatischen Eigenschaften und Eigenschaften gegen Reibung
US5037871A (en) * 1990-05-23 1991-08-06 Eastman Kodak Company Protective overcoat compositions and photographic elements containing same
FR2688604A1 (fr) * 1992-03-16 1993-09-17 Kodak Pathe Procede de traitement photographique et produits photographiques comprenant une surcouche a grains fins.

Also Published As

Publication number Publication date
DE69518268D1 (de) 2000-09-14
JPH07319112A (ja) 1995-12-08
DE69518268T2 (de) 2001-05-23
EP0675402A1 (de) 1995-10-04
FR2718257B1 (fr) 1999-03-19
FR2718257A1 (fr) 1995-10-06

Similar Documents

Publication Publication Date Title
EP0530586B1 (de) Entwicklung von farbphotographischem Aufzeichnungsmaterial
EP0211437A2 (de) Verfahren zur Behandlung farbphotographischer Silberhalogenidmaterialien
JPS62297849A (ja) ハロゲン化銀カラ−写真感光材料の処理方法
JPH02132432A (ja) ハロゲン化銀写真感光材料及びそれを用いた画像形成方法
EP0675402B1 (de) Schutzschicht und diese enthaltende photographische Materialien
JPS62266538A (ja) ハロゲン化銀カラ−写真感光材料
US5948606A (en) Protective top layer and photographic products containing this top layer
JPH0648376B2 (ja) ハロゲン化銀カラ−写真感光材料の処理方法
US5550010A (en) Method for processing photographic products comprising a fine-grain top layer
JPS5981644A (ja) カラ−写真感光材料の処理方法
JPH021844A (ja) ハロゲン化銀写真感光材料
EP0733947B1 (de) Farbumkehrelemente enthaltend eine einen Bleichbeschleuniger freisetzende Verbindung
WO2005111718A1 (en) Method for reducing sensitizing dye stain
US2507154A (en) Direct positive photographs using color developers
JPH02181139A (ja) ハロゲン化銀写真感光材料
EP0568953A2 (de) Verfahren und Zusammensetzungen zum Retuschieren von Filmbildern
JPS6147959A (ja) ハロゲン化銀カラ−写真感光材料の処理方法
US6261747B1 (en) Black-and-white sepia toning kit and method for its use
JPH0619514B2 (ja) 直接ポジ画像形成ハロゲン化銀写真感光材料
JPS5979250A (ja) 銀画像形成方法
JPS61196241A (ja) カラ−反転写真感光材料の処理方法
JPS62100750A (ja) ハロゲン化銀カラ−写真感光材料
JPH07287342A (ja) ハロゲン化銀写真感光材料および画像形成方法
JPS62136639A (ja) 写真感光材料
JPH03181941A (ja) ハロゲン化銀カラー写真印画紙

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE CH DE FR GB LI NL

17P Request for examination filed

Effective date: 19960315

17Q First examination report despatched

Effective date: 19990203

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE CH DE FR GB LI NL

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REF Corresponds to:

Ref document number: 69518268

Country of ref document: DE

Date of ref document: 20000914

REG Reference to a national code

Ref country code: CH

Ref legal event code: NV

Representative=s name: KIRKER & CIE SA

ET Fr: translation filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20001222

Year of fee payment: 7

REG Reference to a national code

Ref country code: FR

Ref legal event code: TP

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 20010327

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20010417

Year of fee payment: 7

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20020205

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20020331

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20020331

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20020331

BERE Be: lapsed

Owner name: *EASTMAN KODAK CY

Effective date: 20020331

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20021001

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20021001

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030327

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20030327

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20050302

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20050331

Year of fee payment: 11

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20061003

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20061130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20060331