电容去离子
氨
电解质
卤水
电极
浓差极化
极化(电化学)
离子
海水淡化
化学
离子交换
废水
膜
化学工程
材料科学
环境科学
环境工程
生物化学
有机化学
物理化学
工程类
标识
DOI:10.1021/acs.est.5c02340
摘要
Flow-electrode capacitive deionization (FCDI) offers an eco-friendly and energy-efficient approach for ammonia recovery from wastewater. However, the presence of coexisting ions significantly impedes recovery efficiency. Here, we investigate the interference mechanisms of coexisting ions on ammonia recovery using a gas-membrane-coupled FCDI system. Results reveal that a single FCDI cell with 10 wt % carbon mass loading achieves optimal performance (SECw = 1.10 kWh m-3, SECN = 34 kWh kg-1 N, and FE = 91.67%), yet these metrics decline markedly after 2 h due to ammonium back diffusion. This back diffusion is strongly correlated with coexisting ion concentrations and carbon loading in flow electrodes. Double current step tests demonstrate that ammonia transmembrane transport is governed by concentration polarization at the membrane/electrolyte interface induced by coexisting ions. To address this, a parallel FCDI cell is employed to discharge high-salinity brine while recovering energy from the salt gradient. Long-term operation (100 h) validates the system's robustness, achieving a concentrated ammonia extract of 954 ppm. This study elucidates critical ion interference mechanisms in FCDI-based ammonia recovery and presents a sustainable strategy for enhancing wastewater resource utilization.
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