Simultaneous removal of ammonia and manganese from electrolytic metal manganese residue leachate using phosphate salt

被引:62
作者
Shu, Jiancheng [1 ,2 ]
Liu, Renlong [1 ,2 ]
Liu, Zuohua [1 ,2 ]
Chen, Hongliang [1 ,2 ]
Tao, Changyuan [1 ,2 ]
机构
[1] Chongqing Univ, Sch Chem & Chem Engn, Chongqing 400044, Peoples R China
[2] Chongqing Key Lab Chem Proc Clean Energy & Resour, Chongqing 400044, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrolytic metal manganese residue leachate; Ammonia; Manganese; Phosphate salt; Precipitate pyrolysis; WASTE-WATER; CHEMICAL PRECIPITATION; LANDFILL LEACHATE; AQUEOUS-SOLUTIONS; STRUVITE; CHINA; MN(OH)(2); OXIDATION; RECOVERY; INDUSTRY;
D O I
10.1016/j.jclepro.2016.06.141
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ammonia and manganese were simultaneously removed from electrolytic metal manganese residue leachate using phosphate salt. The influence of different N:P ratios and pH were investigated. Phase transition and decomposing behavior of precipitates and the characterization of the precipitates pyrolysis were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, differential thermal analysis, and scanning electron microscope. In the laboratory experiment, under the condition of 1:1.15 N:P ratio and 9.5 pH value, removal efficiencies of ammonia and manganese from the residue leachate were achieved 95.0% and 99.9%, respectively, and remaining concentration of orthophosphate was as low as 12 mg L-1. In the process, manganese was first removed as Mn-3(PO4)(2)center dot 7H(2)O, and then ammonia was removed as NH4MgPO4 center dot 6H(2)O. In addition, MgNaPO4, MgHPO4, Mg2P2O7, Na3PO4 and MnO2 were generated during precipitate pyrolysis process, and the ammonia removal efficiency decreased from 84.0% in the first cycle to 66.0% in the fifth, and manganese removal efficiency was approximately 99.0%. Economic evaluation shows that recycling the precipitates for three times could save 68.4% cost on average, compared to the use of pure chemicals. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:468 / 475
页数:8
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