Electrocatalytic degradation of bisphenol a in aqueous solution using β-PbO2/Ti as anode

被引:8
|
作者
Zhu, Chengzhu [1 ]
Hu, Caiju [1 ]
Lu, Jun [2 ]
Wang, Xiaohui [1 ]
Huang, Li [3 ]
Chen, Tianhu [1 ]
机构
[1] Hefei Univ Technol, Sch Resources & Environm Engn, Hefei 230009, Peoples R China
[2] Hefei Univ Technol, Ctr Anal & Measurement, Hefei 230009, Peoples R China
[3] New York State Dept Hlth, Wadsworth Ctr, Albany, NY 12201 USA
关键词
beta-PbO2; anode; electrocatalytic degradation; bisphenol A; OH radicals; ELECTROCHEMICAL DEGRADATION; LEAD DIOXIDE; PHOTOCATALYTIC DEGRADATION; RATE CONSTANTS; OXIDATION; PHENOL; EXPOSURE; WATER; BPA; REACTOR;
D O I
10.1134/S1023193515040163
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this paper, a novel Ti-base beta-PbO2 electrode was successfully prepared by using electrodeposition. The prepared electrode was characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and anode polarization curves. The electrocatalytic degradation efficiency of bisphenol A by using the novel Ti-base beta-PbO2 as anode were examined as a function of supporting electrolyte types and concentrations, electrolysis time, initial BPA concentration, initial pH and current efficiency. The results showed that the removal efficiency of CODCr could reach up to 90.6% after 1.5-h electrolysis at initial bisphenol A concentration of 20 mg L-1, applied voltage of 20 V, electrode spacing of 7 cm, initial pH of 5, and NaCl concentration of 0.020 mol L-1. The electrocatalytic degradation of bisphenol A was induced by hydroxyl radical and other oxidative species attacking parent molecules. The degradation products mainly consisted of small straight chain compounds, CO2 and H2O.
引用
收藏
页码:353 / 361
页数:9
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