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Electrosynthesis and electrochemical characteristics of 2,2′-(4,5-dihydroxy-3-methoxy-1,2-phenylene)bis(3-oxo-3-phenylpropanenitrile): application as a mediator for determination of hydroxylamine at a carbon nanotube modified electrode surface

Electrosynthesis and electrochemical characteristics of an electrodeposited 2,2′-(4,5-dihydroxy-3-methoxy-1,2-phenylene)bis(3-oxo-3-phenylpropanenitrile), DMPP, film on a multi-wall carbon nanotube modified glassy carbon electrode (DMPP-MWCNT-GCE) and its role as a mediator for electrocatalytic oxid...

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Published in:Analytical methods 2014-08, Vol.6 (15), p.5999-6008
Main Authors: Zare, Hamid R., Tashkili, Milad, Khoshro, Hossein, Nematollahi, Davood, Benvidi, Ali
Format: Article
Language:English
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Summary:Electrosynthesis and electrochemical characteristics of an electrodeposited 2,2′-(4,5-dihydroxy-3-methoxy-1,2-phenylene)bis(3-oxo-3-phenylpropanenitrile), DMPP, film on a multi-wall carbon nanotube modified glassy carbon electrode (DMPP-MWCNT-GCE) and its role as a mediator for electrocatalytic oxidation of hydroxylamine are described. Cyclic voltammograms of the DMPP-MWCNT-GCE indicate a pair of well-defined and quasireversible redox couples with surface confined characteristics in a wide pH range of 2.0–12.0. The charge transfer coefficient, α , and the charge transfer rate constant, k s , of DMPP-MWCNT were calculated to be 0.51 and 10.7 ± 1.7 s −1 , respectively. The DMPP-MWCNT-GCE shows a dramatic increase in the peak current and a decrease in the overvoltage of hydroxylamine electrooxidation in comparison with that seen at a bare or MWCNT modified glassy carbon electrode. The kinetic parameters of electron transfer coefficient, α , heterogeneous electron transfer rate constant, k ′, and exchange current density, j 0 , for the oxidation of hydroxylamine at the modified electrode surface were determined using cyclic voltammetry. Differential pulse voltammetry (DPV) exhibits two linear dynamic ranges 1.0–10.0 μmol L −1 and 10.0–300.0 μmol L −1 as well as a detection limit of 0.37 μmol L −1 for hydroxylamine determination. Finally, the modified electrode was successfully used for the determination of spiked hydroxylamine in a tap water sample.
ISSN:1759-9660
1759-9679
DOI:10.1039/C4AY00731J