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dc.contributor.authorStergiou, D. V.en
dc.contributor.authorProdromidis, M. I.en
dc.contributor.authorVeltsistas, P. G.en
dc.contributor.authorEvmiridis, N. P.en
dc.date.accessioned2015-11-24T16:43:47Z-
dc.date.available2015-11-24T16:43:47Z-
dc.identifier.issn0003-2700-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8738-
dc.rightsDefault Licence-
dc.subjectflow-injection analysisen
dc.subjectamperometric biosensorsen
dc.subjectformaldehydeen
dc.subjectairen
dc.subjectsensoren
dc.subjectwateren
dc.subjectstoichiometryen
dc.subjectaciden
dc.subjecto-3en
dc.subjectphen
dc.titleOzone monitoring based on a biosensor concept utilizing a reagentless alcohol oxidase electrodeen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1021/Ac060230h-
heal.identifier.secondary<Go to ISI>://000238665200059-
heal.identifier.secondaryhttp://pubs.acs.org/doi/pdfplus/10.1021/ac060230h-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2006-
heal.abstractAn electrochemical method based on the concept of a biosensor for the monitoring of ozone is described for first time. The proposed method includes two parts: a selective sorbent for ozone, that is, eugenol, and a formaldehyde amperometric biosensor mounted into a flowthrough cell. Ozone adds rapidly to the double bond of the allyl group of eugenol, which has been immobilized onto a hydrophobic C-18 reactor and the so produced formaldehyde is collected into the working buffer solution ( sampler) and pumped to the detector. A multimembrane assembly consisting of an alcohol oxidase-modified nylon membrane sandwiched between an outer polycarbonate and an inner cellulose acetate membrane was fitted onto a Pt electrode and the enzymatically produced H2O2 was monitored at + 0.65 V ( vs Ag/AgCl/ KCl 3 M). Under optimum conditions, a linear calibration curve over the concentration range 3-200 mu g.mL(-1) ozone was constructed. The detection limit (S/N = 3) was calculated at 1.1 mu g.mL(-1) ozone. The proposed method is interferencefree from other gases such as O-2, Ar, N-2, N2O, NOCl, SO2, NH3, and CO2, which were tested at concentrations > 200-fold higher than that of 100 mu g.mL(-1) ozone used for comparison. Besides selectivity, the method is easy to perform and reproducible; its applicability in synthetic gaseous samples is also demonstrated.en
heal.journalNameAnal Chemen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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