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dc.contributor.authorGürkan R.
dc.contributor.authorUlusoy H.I.
dc.contributor.authorAkçay M.
dc.contributor.authorBulut P.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:14:55Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:14:55Z
dc.date.issued2011
dc.identifier.issn1001-0521
dc.identifier.urihttps://dx.doi.org/10.1007/s12598-011-0416-0
dc.identifier.urihttps://hdl.handle.net/20.500.12418/5005
dc.description.abstractA novel catalytic kinetic method is proposed for the determination of Se(IV), Se(VI), and total inorganic selenium in water based on the catalytic effect of Se(IV) on the reduction of Celestine blue by sodium sulfide at pH 7.0 phosphate buffer. The fixed-time method was adopted for the determination and speciation of inorganic selenium. Under the optimum conditions, the two calibration graphs are linear with a good correlation coefficient in the range 2-20 and 20-200 ?g•L -1 of Se(IV) for the fixed-time method at 30°C. The experimental and theoretical detection limits of the developed kinetic method were found to be 0.21 and 2.50 ?g•L -1 for the fixed-time method (3 min). All of the variables that affect the sensitivity at 645 nm were investigated, and the optimum conditions were established. The interference effect of various cations and anions on the Se(IV) determination was also studied. The selectivity of the selenium determination was greatly improved with the use of the strongly cation exchange resin such as Amberlite IR120 plus as long as chelating agents of thiourea and thiosulphate. The proposed kinetic method was validated statistically and through recovery studies in natural water samples. The relative standard deviations (RSDs) for ten replicate measurements of 2, 10, and 20 ?g•L -1 of Se(IV) change between 0.35% and 5.58%, while the RSDs for ten replicate measurements of 3, 6, and 12 ?g•L -1 of Se(VI) change between 0.49% and 1.61%. Analyses of a certified standard reference material (NIST SRM 1643e) for selenium using the fixed-time method showed that the proposed kinetic method has good accuracy. The Se(IV), Se(VI), and total inorganic selenium in lake and river water samples have been successfully determined by this method after selective reduction of Se(VI) to Se(IV). © 2011 The Nonferrous Metals Society of China and Springer-Verlag Berlin Heidelberg.en_US
dc.description.sponsorshiptific Research Council (with F-225 code) for financial support of the present work. Thanks are also due to the many scientists who generously shared their results before publication.en_US
dc.description.sponsorshipGürkan, R.; Department of Chemistry, Faculty of Science, University of Cumhuriyet, Sivas TR-58140, Turkey; email: rgurkan@cumhuriyet.edu.tren_US
dc.language.isoengen_US
dc.relation.isversionof10.1007/s12598-011-0416-0en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectcatalytic effecten_US
dc.subjectCelestine blueen_US
dc.subjectkinetic spectrophotometryen_US
dc.subjectnatural watersen_US
dc.subjectselenium speciationen_US
dc.titleA novel indicator system for catalytic spectrophotometric determination and speciation of inorganic selenium species (Se(IV), Se(VI)) at trace levels in natural lake and river water samplesen_US
dc.typearticleen_US
dc.relation.journalRare Metalsen_US
dc.contributor.departmentGürkan, R., Department of Chemistry, Faculty of Science, University of Cumhuriyet, Sivas TR-58140, Turkey -- Ulusoy, H.I., Department of Chemistry, Faculty of Science, University of Cumhuriyet, Sivas TR-58140, Turkey -- Akçay, M., Department of Chemistry, Faculty of Science, University of Cumhuriyet, Sivas TR-58140, Turkey -- Bulut, P., Department of Chemistry, Faculty of Science, University of Cumhuriyet, Sivas TR-58140, Turkeyen_US
dc.identifier.volume30en_US
dc.identifier.issue5en_US
dc.identifier.endpage487en_US
dc.identifier.startpage477en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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