Selective Ammonium Removal from Synthetic Wastewater by Flow-Electrode Capacitive Deionization Using a Novel K2Ti2O5-Activated Carbon Mixture Electrode

被引:63
|
作者
Lin, Lin [1 ]
Hu, Jiahui [2 ]
Liu, Jiahua [1 ]
He, Xin [1 ]
Li, Bing [2 ]
Li, Xiao-yan [1 ,2 ,3 ]
机构
[1] Tsinghua Univ, Tsinghua Berkeley Shenzhen Inst, Environm Sci & New Energy Technol Res Ctr, Shenzhen 518055, Peoples R China
[2] Tsinghua Shenzhen Int Grad Sch, Shenzhen Engn Res Lab Sludge & Food Waste Treatme, Shenzhen 518055, Peoples R China
[3] Univ Hong Kong, Dept Civil Engn, Environm Engn Res Ctr, Pokfulam, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
POTASSIUM TITANATE; ADSORPTION; DESALINATION; TEMPERATURE; NITROGEN; IONS;
D O I
10.1021/acs.est.0c04383
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ammonium (NH4+) in wastewater is both a major pollutant and a valuable resource. Flow-electrode capacitive deionization (FCDI) is a promising technology for chemical-free and environmentally friendly NH4+ removal and recovery from wastewater. However, the coexisting sodium (Na+) in wastewater, with a similar hydrated radius to NH4+, competes for the adsorption sites, resulting in low NH4+ removal efficiency. Here, potassium dititanate (K2Ti2O5 or KTO) particles prepared by the electrospray method followed by calcination were mixed with activated carbon (AC) powder to form a novel KTO-AC flow-electrode for selective NH4+ removal over Na+. The mixed KTO-AC electrode exhibits a much higher specific gravimetric capacitance in NH4Cl solution than in NaCl solution. Compared with the pure AC electrode in the FCDI tests on NH4+ removal from synthetic wastewater, 25 wt % KTO addition in the electrode mixture increases the adsorption selectivity from 2.3 to 31 toward NH4+ over Na+, improves the NH4+ removal from 28.5% to 64.8% and increases the NH4+ desorption efficiency from 35.6% to over 80%, achieving selective NH4+ recovery and effective electrode regeneration. Based on DFT calculations, NH4+ adsorption on the K2Ti2O5 (0 0 1) surface is more thermodynamically favorable than that of Na+, which contributes to the high NH4+ adsorption selectivity observed.
引用
收藏
页码:12723 / 12731
页数:9
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