Simultaneous Determination of Antimony(III) and Molybdenum(VI) by Adsorptive Stripping Voltammetry Using Quercetin as Complexing Agent

2012 ◽  
Vol 25 (2) ◽  
pp. 439-447 ◽  
Author(s):  
Carlos Rojas ◽  
Verónica Arancibia ◽  
Marisol Gómez ◽  
Edgar Nagles
2013 ◽  
Vol 13 (3) ◽  
pp. 236-241 ◽  
Author(s):  
Deswati Deswati ◽  
Hamzar Suyani ◽  
Safni Safni ◽  
Umiati Loekman ◽  
Hilfi Pardi

A selective and sensitive adsorptive stripping voltammetric (AdSV) procedure for the simultaneous determination of cadmium, copper and lead in the sea water was conducted. The aim of this research is to get optimum condition for simultaneous determination of cadmium, copper and lead. Adsorptive stripping voltammetry has been used for determination of trace amount of Cd(II), Cu(II) and Pb (II) by using calcon as a complexing agent. The parameters studied were variation of calcon concentration, pH, accumulation potential and accumulation time. In this study, the optimum conditions were calcon concentration of 0.6 mM, pH = 4.0, accumulation potential of -0.7 V and accumulation time of 80 sec. At the optimum conditions, the relative standard deviation were 8.78%, 3.12%, and 4.02% for Cd(II), Cu(II) and Pb(II) respectively for eight replicates (n = 8) measurements of 10 μg/L mixed standard solution of Cd(II), Cu(II) and Pb(II). The method was applied to the direct simultaneous determination of Cd(II), Cu(II) and Pb(II) in sea water around Bungus, Padang City. Concentration of Cd(II), Cu(II) and Pb(II) in samples were equal to 1.8 μg/L for Cd(II), 38.6 μg/L for Cu(II) and 0.7 μg/L for Pb(II) with recovery of 87.03%, 98.80%, and 95.73%, respectively.


2013 ◽  
Vol 69 (2) ◽  
pp. 438-442 ◽  
Author(s):  
Shahryar Abbasi ◽  
Abbas Farmany ◽  
Mahmoud Roushani ◽  
Seyede Shima Mortazavi

A simple and sensitive adsorptive stripping voltammetry method was developed for determination of Zn using N-nitrozo-N-phenylhydroxylamine (cupferron) as a selective complexing agent. This complex absorbed on the hanging mercury drop electrode and created a sensitive peak current. The peak current and concentration of zinc accorded with a linear relationship in the range of 0.85–320 ng mL−1. The influence of pH and the nature of supporting electrolytes, concentration of ligand, preconcentration time and applied potential were investigated. The relative standard deviation at a concentration level of 50 ng mL−1 was 1.8%. The method was applied to the determination of zinc in city, river and mineral water samples, with satisfactory results.


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