Robust Fe2+-doped nickel-iron layered double hydroxide electrode for electrocatalytic reduction of hexavalent chromium by pulsed potential method

被引:0
|
作者
Zhifei Wang [1 ,2 ]
Jinbo Xue [1 ]
Yong Li [1 ,2 ]
Qianqian Shen [1 ]
Qi Li [3 ]
Xiaochao Zhang [4 ]
Xuguang Liu [1 ,2 ]
Husheng Jia [1 ,2 ]
机构
[1] Key Laboratory of Interface Science and Engineering in Advanced Materials, Taiyuan University of Technology, Ministry of Education
[2] College of Materials Science and Engineering, Taiyuan University of Technology
[3] School of Materials Science and Engineering, Southwest Jiaotong University
[4] College of Chemistry and Chemical Engineering, Taiyuan University of Technology
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
X703 [废水的处理与利用]; TQ426 [催化剂(触媒)];
学科分类号
080502 ; 081705 ; 083002 ;
摘要
Electrocatalytic reduction of Cr(Ⅵ) to less toxic Cr(Ⅲ) is deemed as a promising technique. Conventional electrocatalytic reduction is always driven by a constant cathodic potential, which exhibits a repelling action to Cr(Ⅵ) oxyanions in wastewater and consequently suppresses reduction kinetics. In order to remarkably accelerate Cr(Ⅵ) electrocatalytic reduction, we applied a pulsed potential on an Fe2+-NiFe LDH/NF electrode synthesized by in situ growth of Fe2+-doped NiFe LDH nanosheets on Ni foam using a spontaneous redox reaction. Under anodic potential section, HCrO4~– anions are adsorbed on the electrode surface and reduced to Cr(Ⅲ) by Fe2+. Then, Cr(Ⅲ) ions are desorbed from the electrode surface under coulombic force. The regeneration of Fe2+and direct reduction of Cr(Ⅵ) are achieved under cathodic potential section. The pulsed potential can achieve complete elimination of Cr(Ⅵ) within 60 min at an initial concentration of 10 mg L-1, and the removal efficiency shows a 60% increase with respect to that under constant cathodic potential.
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页码:73 / 83
页数:11
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