<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE ep-patent-document PUBLIC "-//EPO//EP PATENT DOCUMENT 1.4//EN" "ep-patent-document-v1-4.dtd"><!-- Disclaimer: This ST.36 XML data has been generated from SGML data available on ESPACE discs EPAS Volumes 2003/201 to 203 enriched by the abstract retrieved from the corresponding A2/A1 document - March 2013 - EPO - Dir. Publication - kbaumeister@epo.org --><ep-patent-document id="EP85308436A3" lang="en" country="EP" doc-number="0182658" date-publ="19880113" file="85308436" kind="A3" status="n" dtd-version="ep-patent-document-v1-4"><SDOBI lang="en"><B000><eptags><B001EP>DEFRGB</B001EP></eptags></B000><B100><B110>0182658</B110><B120><B121>EUROPEAN PATENT APPLICATION</B121></B120><B130>A3</B130><B140><date>19880113</date></B140><B190>EP</B190></B100><B200><B210>85308436</B210><B220><date>19851120</date></B220></B200><B300><B310>8429677</B310><B320><date>19841123</date></B320><B330><ctry>GB</ctry></B330></B300><B400><B405><date>19880113</date><bnum>198802</bnum></B405><B430><date>19860528</date><bnum>198622</bnum></B430></B400><B500><B510><B511> 6G 03C  07/32   A</B511></B510><B540><B541>en</B541><B542>Photographic coupler dispersions</B542><B541>fr</B541><B542>Dispersions de coupleur photographique</B542><B541>de</B541><B542>Photographische Kupplerdispersionen</B542></B540></B500><B700><B710><B711><snm>EASTMAN KODAK COMPANY (a New Jersey corporation)</snm></B711><B711><snm>Kodak Limited</snm></B711></B710><B720><B721><snm>Simons, Michael J. Dr.</snm></B721></B720></B700><B800><B840><ctry>DE</ctry><ctry>FR</ctry><ctry>GB</ctry></B840><B880><date>19880113</date><bnum>198802</bnum></B880></B800></SDOBI><abstract id="abst" lang="en"><p id="pa01" num="0001">@ The dark stability of a photographic dye image formed by reaction between a coupler, dispersed in admixture with an involatile solvent, and oxidized p-phenylenediamine colour developing agent is impaired by the presence of a compound comprising a phenolic (or naphtholic moiety in which the acidity of the phenolic hydroxyl group is enhanced by at least one electron-withdrawing substituent in ortho and/or para positions relative to that group. Such a compound may be the coupler itself of the involatile solvent used for its incorporation. This loss in stability can be reduced by introducing into the dispersion a lipophilic anionic surfactant which comprises a sulphate or sulphonate group as the sole hydrophilic group and either a single aliphatic hydrocarbon group having at least 1 carbon atoms or two or more aliphatic hydrocarbon groups which together contain at least 17 carbon atoms. A conventional, i.e. less lipophilic, anionic surfactant may also be used in preparing the coupler dispersion.</p></abstract><search-report-data lang="en" id="srep" srep-office="EP" date-produced=""><doc-page id="srep0001" file="srep0001.tif" type="tif" orientation="portrait" he="295" wi="208" /></search-report-data></ep-patent-document>