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Direct and replacement ion chromatography with potentiometric detection using a silver/silver bromide electrode

dc.contributor.authorTrojanowicz, Mareken_US
dc.contributor.authorPobozy, Ewaen_US
dc.contributor.authorMeyerhoff, Mark E.en_US
dc.date.accessioned2006-04-07T20:56:33Z
dc.date.available2006-04-07T20:56:33Z
dc.date.issued1989en_US
dc.identifier.citationTrojanowicz, Marek, Pobozy, Ewa, Meyerhoff, Mark E. (1989)."Direct and replacement ion chromatography with potentiometric detection using a silver/silver bromide electrode." Analytica Chimica Acta 222(1): 109-119. <http://hdl.handle.net/2027.42/28132>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TF4-44Y6622-8S/2/3ddf74822ccc09771ba41e9395ed7a94en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28132
dc.description.abstractThe use of Ag/AgX electrodes as potentiometric detectors in modern ion chromatography methods is re-examined. Contrary to previous reports, in both flow-injection and chromatographic experiments the Ag/AgBr electrode is shown to exhibit the greatest sensitivity to the widest range of anions tested. For direct detection in non-suppressed ion chromatography systems, use of the Ag/AgBr electrode permits the measurement of separated anions at levels lower than those obtainable by the conventional conductivity method. The Ag/AgBr electrode is further shown to be useful as a sensitive detector in replacement ion chromatography. In this case, all anions separated in a suppressed system are quantitatively replaced by bromide before the effluent passes through the electrochemical detector. Cation measurements can also be made by monitoring the exchange of bromide for co-eluting counter hydroxide ions following the replacement stage of the system.en_US
dc.format.extent729628 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleDirect and replacement ion chromatography with potentiometric detection using a silver/silver bromide electrodeen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055 U.S.A.en_US
dc.contributor.affiliationotherDepartment of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland.en_US
dc.contributor.affiliationotherDepartment of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28132/1/0000583.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0003-2670(00)81884-Xen_US
dc.identifier.sourceAnalytica Chimica Actaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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