催化作用
双酚A
氧原子
激进的
氧气
化学
吸附
降级(电信)
硫酸盐
光化学
无机化学
分子
有机化学
计算机科学
电信
环氧树脂
作者
Yanchun Deng,Yu‐Xin Ye,Yingge He,Jianqiao Xu,Zhuofeng Ke,Xinran Zhang,Gangfeng Ouyang,Xin Yang
标识
DOI:10.1016/j.cej.2024.149782
摘要
The traditional peroxymonosulfate-based advanced oxidation processes (PMS-AOPs) have been significantly limited by the high inputs of oxidants. Herein, an oxygen-coordinated Fe-based single-atom catalyst (Fe-N2O1/OCN) was developed as an efficient pathway to activate peroxymonosulfate (PMS). This catalyst allows for a sharp decrease in PMS dosage while avoiding the release of additional sulfate ions into the treated water. The PAPO generates bisphenol-A (BPA) radicals and SO4•− species adsorbed onto Fe-N2O1/OCN, triggering a chain reaction for BPA degradation through BPA-initiated PAPO. The excellent performance of this system is attributed to the oxygen-coordinated iron center, which weakens the coordination of PMS on Fe-N2O1 and prevents its pre-activation. Furthermore, this PMS activation pathway demonstrates high anti-interference performance and can be continuously conducted in complex water matrices for 20 days, providing a promising alternative to traditional PMS-AOPs.
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