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dc.contributor.authorKostaki, V. T.en
dc.contributor.authorFlorou, A. B.en
dc.contributor.authorProdromidis, M. I.en
dc.date.accessioned2015-11-24T16:57:37Z-
dc.date.available2015-11-24T16:57:37Z-
dc.identifier.issn0013-4686-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10598-
dc.rightsDefault Licence-
dc.subjectelectrochemical treatmenten
dc.subjectgraphite screen-printed electrodesen
dc.subjectchemical sensorsen
dc.subjecturaniumen
dc.subjectvoltammetryen
dc.subjectdesignen
dc.titleElectrochemically induced chemical sensor properties in graphite screen-printed electrodes: The case of a chemical sensor for uraniumen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1016/j.electacta.2011.07.092-
heal.identifier.secondary<Go to ISI>://000295601600105-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0013468611011388/1-s2.0-S0013468611011388-main.pdf?_tid=5f2139e1df690b95d5c22caf474ed0d8&acdnat=1333037176_59a6b30bd93b0177fbb3559993f90e4e-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2011-
heal.abstractWe report for the first time on the possibility to develop chemical sensors based on electrochemically treated, non-modified, graphite screen-printed electrodes (SPEs). The applied galvanostatic treatment (5 mu A for 6 min in 0.1 M H(2)SO(4)) is demonstrated to be effective for the development of chemical sensors for the determination of uranium in aqueous solutions. A detailed study of the effect of various parameters related to the fabrication of SPEs on the performance of the resulting sensors along with some diagnostic experiments on conventional graphite electrodes showed that the inducible analytical characteristics are due to a synergy between electrochemical treatment and ink's solvents. Indeed, the amount of the latter onto the printed working layer controls the achievable sensitivity. The preconcentration of the analyte was performed in an electroless mode in an aqueous solutions of U(VI), pH 4.6, and then, the accumulated species was reduced by means of a differential pulse voltammetry scan in 0.1 M H(3)BO(3), pH 3. Under selected experimental conditions, a linear calibration curve over the range 5 x 10(-9) to 10(-7) M U(VI) was constructed. The 3 sigma limit of detection at a preconcentration time of 30 min, and the relative standard deviation of the method were 4.5 x 10(-9) M U(VI) and >12% (n = 5.5 x 10(-8) M U(VI)), respectively. The effect of potential interferences was also examined. (C) 2011 Elsevier Ltd. All rights reserved.en
heal.publisherElsevieren
heal.journalNameElectrochimica Actaen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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