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dc.contributor.authorTurhan, Seval
dc.contributor.authorUsta, Betül
dc.contributor.authorŞahin, Yücel
dc.contributor.authorUysal, Oktay
dc.contributor.editorLindsay, SJ
dc.date.accessioned2019-10-20T09:14:20Z
dc.date.available2019-10-20T09:14:20Z
dc.date.issued2011
dc.identifier.isbn978-1-11802-935-0
dc.identifier.issn0147-0809
dc.identifier.urihttps://hdl.handle.net/11421/17216
dc.descriptionSymposium on Light Metals / TMS 140th Annual Meeting and Exhibition -- FEB 27-MAR 03, 2011 -- San Diego, CAen_US
dc.descriptionWOS: 000324515400038en_US
dc.description.abstractbauxite 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.description.sponsorshipTMS, TMS Aluminum Commen_US
dc.language.isoengen_US
dc.publisherJohn Wiley & Sonsen_US
dc.relation.ispartofseriesLight Metals
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleDetermination of Oxalate Ion in Bayer Liquor Using Electrochemical Methoden_US
dc.typeconferenceObjecten_US
dc.relation.journalLight Metals 2011en_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Fizik Bölümüen_US
dc.identifier.startpage215en_US
dc.identifier.endpage217en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorŞahin, Yücel


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