Mn2+ oxidation, playing counteractive role in electro-oxidation of ammonia, hinders the generation of free chlorine

被引:3
|
作者
Ma, Xiaoxia [1 ]
Tang, Jinjing [1 ]
Yuan, Yunan [1 ]
Liu, Zuohua [1 ]
Tao, Changyuan [1 ]
机构
[1] Chongqing Univ, Sch Chem & Chem Engn, Chongqing 400044, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROLYTIC MANGANESE RESIDUE; ELECTROCHEMICAL OXIDATION; BEHAVIOR; DYES; MECHANISM; INDUSTRY; REMOVAL;
D O I
10.1039/c6ra09639e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ammonia in electrolytic manganese residue (EMR) constitutes potentially severe environmental risks. As an efficient, environment-friendly technology, electro-oxidation of ammonia in EMR was investigated in the present work. The influence of different metal ions coexisting with ammonia in EMR on the electro-oxidation of ammonia was evaluated and the relevant mechanism was deduced by phase transformation analysis through X-ray diffraction, X-ray fluorescence, scanning electron microscopy, flame atomic absorption spectrometry, and spectrophotometry. Results showed that (1) Mn2+, Ca2+, Mg2+, Na+, and K+ coexist with ammonia in the water-leach liquor of EMR, (2) Mn2+ inhibits the reaction whereas Ca2+ and Mg2+ demonstrate no distinct influence on the electro-oxidation of ammonia, and (3) Mn2+ and Cl- react emulously on the anode. MnO2 hinders the generation of free chlorine; thus, the presence of Mn2+ exerts a crucial impact on ammonia removal. So, it can be considered that further utilization of EMR can be realized by recycling Mn2+ first and then removing effectively ammonia through electro-oxidation method.
引用
收藏
页码:90502 / 90508
页数:7
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