Voltammetric trace metal determinations by cathodic and anodic stripping voltammetry in environmental matrices in the presence of mutual interference

Citation
C. Locatelli et G. Torsi, Voltammetric trace metal determinations by cathodic and anodic stripping voltammetry in environmental matrices in the presence of mutual interference, J ELEC CHEM, 509(1), 2001, pp. 80-89
Citations number
43
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
ISSN journal
15726657 → ACNP
Volume
509
Issue
1
Year of publication
2001
Pages
80 - 89
Database
ISI
SICI code
Abstract
Arsenic(III), selenium(IV), copper(II), lead(II), cadmium(II), zinc(II) and manganese(II) have been determined in environmental matrices by differenti al pulse cathodic (DPCSV) and anodic (DPASV) stripping voltammetry. The vol tammetric measurements were carried out using, as the working electrode, a stationary mercury electrode, and a platinum electrode and a Ag \ AgCl \ KC l(sat) electrode as the auxiliary and reference electrode, respectively. An ammonia + ammonium chloride buffer of pH 9.0 was employed as the supportin g electrolyte. The analytical procedure was verified by the analysis of the standard reference materials: Sea Water BCR-CRM 403, Estuarine Sediment BC R-CRM 277, Ulva Lactuca BCR-CRM 279 and Mussel Tissue BCR-CRM 278. The prec ision and accuracy, expressed as relative standard deviation and relative e rror, respectively, were lower than 5% in all cases, while the detection li mit for each element was around 10 (9) mol l (- 1). In the presence of high reciprocal interference, the standard addition method considerably improve d the resolution of the voltammetric technique. The analytical procedure wa s transferred and applied to samples drawn in the Goro Bay (Ferrara, Italy) . (C) 2001 Elsevier Science B.V. All rights reserved.