Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/16686
Title: Trace level voltammetric determination of lead and cadmium in sediment pore water by a bismuth-oxychloride particle-multiwalled carbon nanotube composite modified glassy carbon electrode
Authors: Cerovac Sandra
Guzsvány Valéria
Kónya Zoltan
Ashrafi M.Amir
Švancara Ivan
Rončević Srđan 
Akos Kukovecz
Dalmacija Božo 
Vytřas Karel
Issue Date: 2015
Journal: Talanta
Abstract: © 2014 Elsevier B.V. All rights reserved. Two multiwalled carbon nanotubes-based composites modified with bismuth and bismuth-oxychloride particles were synthesized and attached to the glassy carbon electrode substrate. The resultant configurations, Bi/MWCNT-GCE and BiOCl/MWNT-GCE, were then characterized with respect to their physicochemical properties and electroanalytical performance in combination with square-wave anodic stripping voltammetry (SWASV). Further, some key experimental conditions and instrumental parameters were optimized; namely: the supporting electrolyte composition, accumulation potential and time, together with the parameters of the SWV-ramp. The respective method with both electrode configurations has then been examined for the trace level determination of Pb2+ and Cd2+ ions and the results compared to those obtained with classical bismuth-film modified GCE. The different intensities of analytical signals obtained at the three electrodes for Pb2+ and Cd2+ vs. the saturated calomel reference electrode had indicated that the nature of the modifiers and the choice of the supporting electrolyte influenced significantly the corresponding stripping signals. The most promising procedure involved the BiOCl/MWCNT-GCE and the acetate buffer (pH 4.0) offering limits of determination of 4.0 μg L-1 Cd2+ and 1.9 μg L-1 Pb2+ when accumulating for 120 s at a potential of -1.20 V vs. ref. The BiOCl/MWCNT electrode was tested for the determination of target ions in the pore water of a selected sediment sample and the results agreed well with those obtained by graphite furnace atomic absorption spectrometry.
URI: https://open.uns.ac.rs/handle/123456789/16686
ISSN: 0039-9140
DOI: 10.1016/j.talanta.2014.12.002
Appears in Collections:PMF Publikacije/Publications

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