石墨烯
化学
钴
降级(电信)
氧化物
异质结
钴铁氧体
三氯生
材料科学
无机化学
化学工程
光化学
光电子学
纳米技术
冶金
医学
病理
工程类
电信
计算机科学
作者
Malihe Moazeni,Karim Ebrahimpour,Mahmoud Etebari,Jorge Bedia,Kun‐Yi Andrew Lin,Afshin Ebrahimi
标识
DOI:10.1016/j.jwpe.2022.103214
摘要
Sulfate radical-based-advanced oxidation processes (SR-AOPs) have been recently considered for micropollutants degradation in water treatment. In the present study, cobalt ferrite (CoFe 2 O 4 ), a metal-organic framework (MOFs) (MIL-101(Fe)), and graphene oxide (GO) were used to synthesize a novel heterostructure, CoFe 2 O 4 /MIL-101(Fe)/GO (C/M/G), through a hydrothermal method. The structural properties of C/M/G were determined by several characterization methods. The samples tested in the degradation of triclosan (TCS) with peroxymonosulfate (PMS), were able to activate it generating the highly active hydroxyl (HO • ) and sulfate radicals (SO 4 •− ). The effect and interaction of controlling parameters on TCS removal were investigated. Complete removal of TCS (500 μg/L) was achieved with pH 5, 0.04 g/L catalyst, and 8 μM PMS in only 30 min. The TCS removal declined obviously in the presence of radical scavengers and coexisting ions. The leachings of cobalt (Co) and iron (Fe) ions were lower than those of other CoFe 2 O 4 composites coupled with PMS. Moreover, this process demonstrated high performance in the treatment of TCS in tap and well water. Accordingly, the C/M/G/PMS system seems to be a highly effective and environmentally compatible process for micropollutant degradation in water treatment. • C/M/G is a novel heterostructure for PMS activation in TCS degradation from water. • TCS can mineralize by C/M/G coupled with PMS process. • The PMS was an effective variable on TCS removal by C/M/G/PMS process. • Co and Fe leaching decreased after C/M/G compared with CoFe 2 O 4 based catalysts.
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