Catalytic Cathodic Stripping Voltammetry of 5-Phenyl-1,3,4-oxadiazole-2-thiol in the Presence of Nickel(II) and Cobalt(II) Ions

2004 ◽  
Vol 69 (8) ◽  
pp. 1600-1609
Author(s):  
Sławomira Skrzypek ◽  
Agata Michałek ◽  
Witold Ciesielski ◽  
Michał Kasprzak

5-Phenyl-1,3,4-oxadiazole-2-thiol (POT) and the systems Ni(II)-POT-acetate buffer, Co(II)-POT-acetate buffer were investigated by differential-pulse cathodic stripping voltammetry (DPCSV). The results of the voltammetric measurements show that POT gives a DPCSV signal at about -0.2 V vs Ag|AgCl. The presence of both POT and nickel(II) ions gives rise to a new peak at about -0.6 V; in the presence of cobalt(II) ions a new peak appears at -1.1 V. Based on published results obtained for other sulfur compounds in the presence of Ni(II) or Co(II) ions, the peak at -0.6 V is ascribed to catalytic reduction of Ni(II), and the peak at -1.1 V to hydrogen catalytic discharge. Optimum conditions have been found for the determination of POT by DPCSV. A linear dependence has been found only for the catalytic Ni(II) peak in the region 10-8-10-7 M POT. The calculated limit of detection and limit of quantification are 3.4 × 10-9 and 1.1 × 10-8 mol l-1, respectively.

2015 ◽  
Vol 7 (5) ◽  
pp. 2121-2128 ◽  
Author(s):  
Parisa Sharifian ◽  
Alireza Aliakbar

Method and conditions: determination of trace amounts of Se(IV) by adsorptive cathodic stripping voltammetry at the Bi/Hg film electrode in an open circuit system; limit of detection: 0.07 ng mL−1; limit of quantification: 0.25 ng mL−1; RSD: 2.4% (for five replications of 5 ng mL−1 of Se(iv)); analytical range: 2–50 ng mL−1; interference: selective for Se(iv) – no interference; application: determination of Se(iv) in vegetable, fruits and water samples.


2011 ◽  
Vol 76 (2) ◽  
pp. 131-142 ◽  
Author(s):  
Dariusz Guziejewski ◽  
Sławomira Skrzypek ◽  
Adam Łuczak ◽  
Witold Ciesielski

A new, rapid and very sensitive electrochemical method for the determination of a new pesticide clothianidin in tap and river water was developed. The electrochemical reduction and determination of clothianidin have been carried out at a hanging mercury drop electrode (HMDE) in various aqueous solutions in the pH range of 2–10 by cyclic voltammetry (CV) and cathodic stripping square wave voltammetry (SW CSV). The best results were obtained for the clothianidin determination by SW CSV method in 0.04 mol l–1 Britton Robinson buffer at pH 8.1. Various conditions of the procedure were checked. Elaborated electroanalytical procedure enable clothianidin determination in the concentration range of 2.0 × 10–8–9.9 × 10–7 mol l–1. The limit of detection (LOD) and limit of quantification (LOQ) were obtained as 2.00 × 10–9 and 2.36 × 10–8 mol l–1, respectively. Precision and accuracy of the developed method were checked by recovery studies in spiked tap and river water. The voltammetric determination has been validated using HPLC with UV detection.


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