化学
双金属片
单线态氧
降级(电信)
复合数
核化学
激进的
尼泊金甲酯
渗滤液
化学需氧量
催化作用
化学工程
废水
环境化学
氧气
有机化学
材料科学
环境工程
工程类
复合材料
电信
防腐剂
计算机科学
作者
Cui Lai,Huchuan Yan,Dongbo Wang,Shiyu Liu,Xuerong Zhou,Xiaopei Li,Mingming Zhang,Ling Li,Yukui Fu,Fuhang Xu,Xiaofeng Yang,Xiuqin Huo
出处
期刊:Chemosphere
[Elsevier BV]
日期:2021-12-30
卷期号:293: 133472-133472
被引量:85
标识
DOI:10.1016/j.chemosphere.2021.133472
摘要
Peroxymonosulfate (PMS)-based advanced oxidation processes for wastewater treatment have received extensive attention in the past years. Here, a novel Mn, Ce co-modified g-C3N4 (MnCe-CN) composite was successfully synthesized by one-step pyrolysis for activating PMS. The physical and chemical characterization of MnCe-CN/PMS was conducted, indicating that Mn and Ce were evenly distributed on g-C3N4 and existed in the form of Mn-N structure and CeO2, respectively. The MnCe-CN/PMS system could effectively degrade pollutants such as acetaminophen (ACT), methylparaben (MeP), p-nitrophenol (PNP), and 2,4-dichlorophenol (2,4-DCP). Among them, 2,4-DCP could be rapidly degraded, reaching 100% within 30 min. The masking experiments and electrochemical testing results revealed that 2,4-DCP was degraded via superoxide radicals (O2˙-), singlet oxygen (1O2), and electron transfer path. The cyclic experiments and real water treatment experiments testified that the oxidative system had excellent stability and applicability. This study provides a facile synthetic method to fabricate bimetallic co-modified g-C3N4 for the enhancement of PMS activation.
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