Electrochemical oxidation of cinnamic acid with Mo modified PbO2 electrode: Electrode characterization, kinetics and degradation pathway

被引:105
|
作者
Dai, Qizhou [1 ]
Zhou, Jiazhong [1 ]
Meng, Xiaoyang [2 ]
Feng, Daolun [3 ]
Wu, Chengqiang [1 ]
Chen, Jianmeng [1 ]
机构
[1] Zhejiang Univ Technol, Coll Biol & Environm Engn, Hangzhou 310032, Zhejiang, Peoples R China
[2] Georgia Inst Technol, Sch Civil & Environm Engn, Atlanta, GA 30332 USA
[3] Shanghai Maritime Univ, Coll Marine Sci & Engn, Shanghai 200135, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Transition metal; Cinnamic acid; Electrochemical oxidation; PbO2; electrode; Degradation mechanism; WASTE-WATER TREATMENT; LEAD DIOXIDE ANODE; PB/PBO2; ELECTRODE; METHYLENE-BLUE; TI/SNO2-SB/PBO2; MINERALIZATION; DYE; OPTIMIZATION; PARAMETERS; REMOVAL;
D O I
10.1016/j.cej.2015.12.054
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A novel molybdenum modified PbO2 electrode was successfully prepared with the method of electrode position. The SEM and XRD were employed to study the surface morphology of electrodes, which indicated that the modified PbO2 electrode had a larger effective area and more compact film. Electrochemical degradation of cinnamic acid (CA) in aqueous solution with Mo-PbO2 electrode and PbO2 electrode were investigated. The results showed that the Mo-PbO2 electrode had a better effect of CA removal. The operational parameters influencing the electrochemical degradation of CA with Mo-PbO2 electrode were optimized and the results revealed that the electrochemical degradation of CA followed the pseudo-first-order kinetics and the optimal removal of CA and COD were 85.51% and 25.79% after 120 min on condition of the electrolyte concentration, initial concentration of CA, current density and initial value of pH were 0.1 mol/L, 300 mg/L, 10 mA/cm(2) and 3.4, respectively. The degradation mechanism of CA in electrochemical oxidation with Mo-PbO2 electrode was analyzed and the main degradation pathway of CA was proposed based on the intermediates identified by IC and GC-MS. (C) 2015 Published by Elsevier B.V.
引用
收藏
页码:239 / 246
页数:8
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