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Investigation on electro-catalytic oxidation properties of carbon nanotube–Ce-modified PbO2 electrode and its application for degradation of m-nitrophenol

In this work a carbon nanotube–Ce-modified PbO2 (CNT–Ce–PbO2) electrode was prepared by electrodeposition method, and compared with pure PbO2, Ce–PbO2, and CNT–PbO2 electrodes. The direct and indirect oxidation capacities of prepared electrodes in electro-catalytic oxidation processes were investiga...

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Bibliographic Details
Published in:Arabian journal of chemistry 2019-07, Vol.12 (5), p.709-717
Main Authors: Duan, Xiaoyue, Zhao, Yuanyuan, Liu, Wei, Chang, Limin
Format: Article
Language:English
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Summary:In this work a carbon nanotube–Ce-modified PbO2 (CNT–Ce–PbO2) electrode was prepared by electrodeposition method, and compared with pure PbO2, Ce–PbO2, and CNT–PbO2 electrodes. The direct and indirect oxidation capacities of prepared electrodes in electro-catalytic oxidation processes were investigated by cyclic voltammetry and hydroxyl radical production tests, respectively. The electro-catalytic activity of electrodes was examined by electro-catalytic oxidation of a model pollutant of m-nitrophenol (m-NP). Besides, high-performance liquid chromatography (HPLC) was also employed to identify the products resulting from the electro-catalytic oxidation of m-NP and the degradation mechanism of m-NP was proposed. Results show that the CNT–Ce–PbO2 anode has higher direct and indirect oxidation capacities than pure PbO2, Ce–PbO2, and CNT–PbO2 anodes. In the electro-catalytic oxidation of m-NP, the m-NP can be oxidized and degraded at all anodes, and the oxidation reactions of m-NP follow first-order kinetics. m-NP and TOC removal efficiencies are about 0.987 and 0.622 after electrolysis of 120 min and a maximum first-order rate constant of 0.036 min−1 is achieved at the CNT–Ce–PbO2 anode, which are obviously higher than those of the other three kinds of anodes. Keywords: Electro-catalytic oxidation, PbO2 electrode, Carbon nanotube, Ce, m-Nitrophenol
ISSN:1878-5352
DOI:10.1016/j.arabjc.2014.11.025