催化作用
膜
双酚A
双金属片
化学
单线态氧
化学工程
热解
腐植酸
降级(电信)
无机化学
氧气
有机化学
生物化学
工程类
电信
肥料
计算机科学
环氧树脂
作者
Jian Ye,Jiangdong Dai,Lulu Wang,Chunxiang Li,Yongsheng Yan,Guo‐Yu Yang
标识
DOI:10.1016/j.jcis.2020.10.082
摘要
Abstract Currently, carbon-based catalysts integrated with macroporous catalytic membrane have aroused considerable attention for environmental remediation because of its practicability and high efficiency. Herein, nitrogen doped carbon nanotube hybrids (Fe-Co@NC-CNTs) decorated with multiple active species (Fe3Co7/CoFe2O4@Fe/Co N C) were designed through N-molecule assisted pyrolysis of bimetallic (Fe/Co) metal–organic frameworks, and then immobilized on poly(vinylidene fluoride) (PVDF) membrane to construct macroporous Fe-Co@NC-CNTs/PVDF catalytic membrane via directional freezing technique, where active sites were efficiently exposed for oxidants and target pollutants. As expected, Fe-Co@NC-CNTs/PVDF membrane successfully achieved almost 100% bisphenol A (BPA) degradation after 40 min via PMS activation, which was significantly overperformed the majority of conventional carbon-based catalysts. Besides, we found that Fe-Co@NC-CNTs/PVDF membrane not only exhibited ideal catalytic and self-cleaning property in humic acid (HA)-BPA coexistence system, but also maintained the excellent reusability and ultrahigh water flux (10464.45 L m−2 h−1) even after 5 cycles. Notably, in EPR analysis and quenching experiments, it was found that sulfate radicals (SO4·− and ·OH) and singlet oxygen (1O2) participated the degradation process while 1O2 made a major contribution. More significantly, this study is very meaningful for the development of novel catalytic self-cleaning membranes with PMS activation.
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