吸附
全氟辛酸
电场
化学
离解(化学)
化学工程
离子交换
静电相互作用
卤素
离子
环境化学
有机化学
烷基
化学物理
物理
量子力学
工程类
作者
Zixuan Nie,Chengji Sui,Xiaobin Xie,Huan Liu,Yanzhan Chen,Shou‐Qing Ni,Bin Cai,Lingshuai Kong,Jinhua Zhan
标识
DOI:10.1016/j.seppur.2023.124980
摘要
In this study, a FeOCl adsorbent was demonstrated to rapidly remove perfluorocarboxylic acids (PFCAs). The unique coordination environment led to preferential dissociation of the Cl− in the FeOCl lattice by hydration, forming a high-intensity interfacial micro-electric field. The interfacial micro-electric field could apply an electric driving force to increase the external diffusion flux of PFCAs, thus achieving rapid adsorption (adsorption equilibrium time ∼10 min). In addition, the interfacial micro-electric field excited synergistic adsorption of multiple interactions (complexation, electrostatic interaction, and halogen-bonding interaction), being able to reach 277.01 mg/g for perfluorooctanoic acid (PFOA). Additionally, we developed a continuous flow column using FeOCl to demonstrate its potential for decontaminating drinking water with PFCAs at environmentally relevant concentrations. The FeOCl adsorbent exhibited a bed life of 125,000 BV upon reaching breakthrough concentration of breakthrough concentration of 70 ng/L in dynamic adsorption experiment, which outperformed conventional activated carbon F400D and ion exchange resin IRA67 adsorbents. Spent FeOCl absorbent could be easily regenerated in mild regeneration conditions and maintained a high PFOA removal in subsequent usage cycles. FeOCl demonstrated great potential in the purification of PFCA-contaminated water for household or municipal applications.
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