Synchronously improved permeability, selectivity and fouling resistance of Fe-N-C functionalized ceramic catalytic membrane for effective water treatment: The critical role of Fe

结垢 化学 选择性 催化作用 吸附 生物污染 陶瓷膜 渗透 化学工程 水处理 膜污染 活性炭 陶瓷 无机化学 有机化学 环境工程 生物化学 工程类
作者
Yi Gao,Guanlong Wang,Xing Wang,Xiaoli Dong,Xiufang Zhang
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:463: 132888-132888 被引量:51
标识
DOI:10.1016/j.jhazmat.2023.132888
摘要

Constructing catalytic membrane simultaneously displaying high permeability, selectivity and antifouling performance in water treatment remains challenging. Herein, the surface and pore channels of the ceramic membrane were co-functionalized with nitrogen doped carbon supported Fe catalyst (CN-F), and the Fe content was varied to investigate its effect on performance of CN-F coupled with peroxymonosulfate (PMS) activation (CN-F/PMS) for water treatment. Results confirmed the introduced Fe (in Fe-N coordination form) greatly enhanced the permeability, selectivity and fouling resistance of CN-F. Optimal CN-F3/PMS achieved 96.5% removal and 52.1% mineralization of sulfamethoxazole in short retention duration (2.7 min), whose performance was 5.4 and 6.7 times higher than that of nitrogen doped carbon functionalized ceramic catalytic membrane (CN/PMS) and CN-F3 filtration alone, respectively. CN-F3/PMS also efficiently inhibited fouling on both surface and pores with 2.8 and 2.4 times lower flux loss than that of CN/PMS and CN-F3 filtration alone, respectively. Moreover, CN-F3/PMS displayed superior performance in long-term treatment of real coking wastewater. The outstanding performance of CN-F was mainly attributed to the dual role of supported Fe, which served as hydrophilic site for enhanced water permeation and major active site for PMS adsorption and reduction into reactive species (mainly high-valent Fe(IV)=O species) towards pollutant elimination.
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