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Frontiers of Environmental Science & Engineering

ISSN 2095-2201

ISSN 2095-221X(Online)

CN 10-1013/X

Postal Subscription Code 80-973

2018 Impact Factor: 3.883

Front. Environ. Sci. Eng.    2015, Vol. 9 Issue (4) : 605-614    https://doi.org/10.1007/s11783-014-0703-8
RESEARCH ARTICLE
Vanadium and molybdenum concentrations in particulate from Palermo (Italy): analytical methods using voltammetry
Diana AMORELLO, Santino ORECCHIO()
Department of Biological Chemical and Pharmaceutical Sciences and Technologies, Palermo University, Palermo I-90128, Italy
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Abstract

The main purpose of this work was to develop a reliable method for the determination of vanadium (V) and molybdenum (Mo) in atmosphere particles or aerosols because they can not be readily measured using conventional techniques. For this research, 30 particulate samples were collected from five different stations located at Palermo, Italy. We used the catalytic adsorptive stripping voltammetry and differential pulsed voltammetry to measure V and Mo in atmospheric particulate, respectively. The represented method includes advantages of high sensitivity, high selectivity, simplicity, reproducibility, speed and low costs. The quantification limits for V and Mo are, respectively, 0.57 and 0.80 ng·m−3. The precision, expressed as relative standard deviation (RSD %), was about 2% for both metals. The mean recoveries of added V and Mo were about 99.5% and ranged from 97% to 101%. Vanadium concentrations in particulate samples collected in Palermo area ranged from 0.57 to 7.7 ng·m−3, while Mo concentrations were in the range 0.8–51 ng·m−3. In many cases the concentrations of two elements in the particulate samples fall below the detection limits. The mean concentrations for V and Mo in particulate samples, collected in Palermo area, were respectively 3.1 and 5.9 ng·m−3.

Keywords vanadium      molybdenum      particulate      voltammetry      Palermo     
Corresponding Author(s): Santino ORECCHIO   
Online First Date: 07 May 2014    Issue Date: 25 June 2015
 Cite this article:   
Diana AMORELLO,Santino ORECCHIO. Vanadium and molybdenum concentrations in particulate from Palermo (Italy): analytical methods using voltammetry[J]. Front. Environ. Sci. Eng., 2015, 9(4): 605-614.
 URL:  
https://academic.hep.com.cn/fese/EN/10.1007/s11783-014-0703-8
https://academic.hep.com.cn/fese/EN/Y2015/V9/I4/605
Fig.1  Location of sampling stations in Palermo
parameter molybdenum vanadium
technique DPV AdSV
initial potential /(mV) 0 –250
final potential /(mV) –700 –650
current range /(µa)
potential scan rate /(mV·s−1) 20 20
potential of deposition /(mV) –150
cycle /n° 3 2
deposition time /s 100
stirring rate /(r·min−1) 300 300
size of the drop /(a.u.) 60 30
delay time before potential sweep /s 5 5
working electrode hanging mercury drop electrode hanging mercury drop electrode
auxiliary electrode glassy carbon glassy carbon
reference electrode Ag/AgCl/KCl (sat.) Ag/AgCl/KCl (sat.)
flowing gas N2 (99.998%) N2 (99.998%)
electrolite NaClO3 HAc-NaAc pH 4,8
reagent mandelic acid chloranilic acid+ KBrO3
Tab.1  Operating parameters for the voltammetric analysis of the solutions obtained from particulate samples
Fig.2  Voltammetric curves for vanadium (a) and molybdenum (b)
Fig.3  Calibration graphs for V (a) and Mo (b)
Fig.4  Concentrations of airborne particulate
Fig.5  Concentrations of V (a) and Mo (b) in airborne particulate
Fig.6  Enrichment factors (EI) for vanadium (a) and molybdenum (b)
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