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dc.contributor.authorTurhan, S.
dc.contributor.authorUsta, B.
dc.contributor.authorŞahin, Y.
dc.contributor.authorUysal, O.
dc.date.accessioned2019-10-20T14:27:51Z
dc.date.available2019-10-20T14:27:51Z
dc.date.issued2011
dc.identifier.isbn9781118029350
dc.identifier.issn0147-0809
dc.identifier.urihttps://hdl.handle.net/11421/17877
dc.descriptionLight Metals 2011 - TMS 2011 Annual Meeting and Exhibition -- 27 February 2011 through 3 March 2011 -- San Diego, CA -- 84639en_US
dc.description.abstractThe Bayer process can be summarized as the digestion of bauxite with caustic liquor and the subsequent precipitation of hydrated alumina [1]. Most bauxite contains organic compounds in various amounts. Depending upon the digestion conditions, 5-10% of the organic carbon is converted to sodiumoxalate [2]. When sodiumoxalate, if not controlled in Bayer process, builds up to a certain level of supersaturation, it precipitates out in the hydrate precipitator tank. This co-precipitation affects the quality of alumina [3]. In this study, we investigated the electrochemical determination of oxalate ion by using differential puls voltammetry in Bayer liquor. A linear relationship between oxalate concentration and current response was obtained with good reproducibility of the current.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBayer Liquoren_US
dc.subjectOxalateen_US
dc.subjectPencil Graphite Electrode, Differential Pulse Voltammetryen_US
dc.titleDetermination of oxalate ion in bayer liquor using electrochemical methoden_US
dc.typeconferenceObjecten_US
dc.relation.journalTMS Light Metalsen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Kimya Bölümüen_US
dc.identifier.startpage215en_US
dc.identifier.endpage217en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US]


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