Enhanced electrochemical degradation of 2,4-dichlorophenol with the assist of hydrochar

被引:21
|
作者
Cao, Weiming [1 ]
Zeng, Chaju [1 ]
Guo, Xiaofei [1 ]
Liu, Qiang [2 ]
Zhang, Xiaolei [2 ]
Mameda, Naresh [3 ]
机构
[1] Shanghai Univ, Coll Sci, Shanghai 200444, Peoples R China
[2] Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
[3] Kyungpook Natl Univ, Adv Inst Water Ind, 80 Daehak Ro, Daegu 41566, South Korea
基金
中国国家自然科学基金;
关键词
2,4-Dichlorophenol; Hydrochar; Electrolysis; Reactive oxygen species; FREE-RADICALS; OXIDATION; CARBON; ADSORPTION; MECHANISM; REMOVAL; ACID;
D O I
10.1016/j.chemosphere.2020.127643
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Effective treatment of 2,4-dichlorophenol (2,4-DCP) in wastewater is essential, as it could pose great threat to the environment. A hydrothermal biochar (hydrochar) was used to assist the electrochemical oxidation treatment of 2,4-DCP. The removal of 2,4-DCP using hydrochar in anode and cathode area with and without proton exchange membrane (PEM) under 3-9 V of electrolysis was investigated. Enhanced 2,4-DCP degradation in the anode area was achieved compared with the adsorption or electrolysis alone. The highest 2,4-DCP removal (similar to 76%) was obtained using the hydrochar in the anode area with PEM under 9 V. The mechanism for the 2,4-DCP removal during the electrolysis included adsorption by hydrochar and electrochemical degradation by the reactive oxygen species (ROS) generated by the electrode as well as the persistent free radicals (PFR) on hydrochar. The center dot OH produced from anode was the predominant ROS contributing to the 2,4-DCP degradation under 9 V of electrolysis. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页数:9
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