Electrochemical-catalytic reduction of nitrate over Pd-Cu/γAl2O3 catalyst in cathode chamber: Enhanced removal efficiency and N2 selectivity

被引:116
|
作者
Zhang, Zhiqiang [1 ]
Xu, Yongpeng [1 ]
Shi, Wenxin [1 ]
Wang, Wei [1 ]
Zhang, Ruijun [1 ]
Bao, Xian [1 ]
Zhang, Bing [1 ]
Li, Li [1 ]
Cui, Fuyi [1 ]
机构
[1] Harbin Inst Technol, Sch Municipal & Environm Engn, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
基金
中国国家自然科学基金;
关键词
Pd-Cu/gamma Al2O3 catalyst; Nitrate; Electrochemical-catalytic; Current efficiency; PD-CU; ELECTROCATALYTIC REDUCTION; SUPPORTED CATALYSTS; NITRITE REDUCTION; AQUEOUS-SOLUTION; EXCHANGE RESIN; WATER; ADSORPTION; GROUNDWATER; METAL;
D O I
10.1016/j.cej.2016.01.063
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Pd-Cu/gamma Al2O3 catalysts were prepared by impregnation method and introduced into the cathode chamber of a divided electrochemical denitrification cell with two graphite plates as the cathode and anode, to enhance the nitrate removal efficiency and N-2 selectivity. The Pd-Cu/gamma Al2O3 catalysts were characterized by transmission electron microscope (TEM), X-ray diffraction (XRD), specific surface area measurements (BET) and inductively coupled plasma-atomic emission spectrometry (ICP-AES). In the rationally designed electrochemical-catalytic (ECC) system, the as-prepared catalyst could significantly enhance the nitrate degradation rate to 1.08 ma at current density of 10 mA/cm(2), which was approx. 2.5 times compared with the electrochemical (EC) system without catalysts adding in. Additionally, a higher nitrogen selectivity of 80.37% was obtained under the same experiment condition. The improved performances were likely due to the presence of a catalytic reduction reaction of nitrate with the appropriate amount of hydrogen generated by electrolysis as reductant. Significantly, the current efficiency was calculated and enhanced value of 20-40% (depended on current density) was obtained in the ECC process with a catalyst content of 1.0 g/L. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:201 / 208
页数:8
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