Mechanistic investigation of the conductive ceramic Ebonex® as an anode material

被引:85
作者
Bejan, Dorin [1 ]
Malcolm, John D. [1 ]
Morrison, Lyndsay [1 ]
Bunce, Nigel J. [1 ]
机构
[1] Univ Guelph, Dept Chem, Electrochem Technol Ctr, Guelph, ON N1G 2W1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Ebonex; Conductive ceramic; Electrochemical oxidation; Mineralization; ADVANCED OXIDATION PROCESSES; WASTE-WATER TREATMENT; HYDROXYL RADICALS; ELECTROCHEMICAL INCINERATION; ORGANIC POLLUTANTS; ELECTRODE MATERIAL; DIAMOND ELECTRODE; OXALIC-ACID; PERFORMANCE; ELECTROOXIDATION;
D O I
10.1016/j.electacta.2009.04.057
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
Ebonex (R) is a conductive and corrosion-resistant ceramic with the approximate composition Ti4O7. Anodic and/or cathodic polarization of a pair of Ebonex electrodes changed their surface composition, as shown by the development of a potential difference between them. In consequence, the activity of an Ebonex anode with respect to oxidation of an organic substrate depends on its past history. The anodic oxidation of p-nitrosodimethylaniline, which has been used as a model compound for the detection and quantitation of hydroxyl radicals, was studied in order to determine whether hydroxyl radicals are produced upon anodic polarization of Ebonex. The results were ambiguous, because direct oxidation of this substrate and oxidation of water to hydroxyl radicals occur at similar potentials. p-Benzoquinone (BQ) was found to be a more satisfactory mechanistic probe because it is resistant to direct oxidation. The rates of both disappearance and overall mineralization of BQ at Ebonex were intermediate between the corresponding rates at boron-doped diamond (BDD) and Ti/IrO2-Ta2O5 anodes, which promote one-electron and two-electron oxidations respectively. However. it is not yet clear whether mineralization is initiated by hydroxyl radicals formed in lower yield than at 'active' materials such as BDD, or whether oxidation involves less reactive intermediates such as HO2 radicals. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5548 / 5556
页数:9
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