过氧乙酸
钴铁氧体
化学
钴
降级(电信)
污染
铁氧体(磁铁)
材料科学
无机化学
有机化学
化学工程
复合材料
过氧化氢
电气工程
工程类
生物
生态学
作者
Gaofeng Zhou,Yongsheng Fu,Runyu Zhou,Li Zhang,Linyue Zhang,Jiewen Deng,Yiqing Liu
标识
DOI:10.1016/j.psep.2022.02.031
摘要
In this study, a novel heterogeneous peracetic acid (PAA)-based advanced oxidation process (AOP), viz. cobalt ferrite combined with PAA (CoFe 2 O 4 /PAA), was used to degrade organic contaminants . The best pH for rhodamine B (RhB) degradation in CoFe 2 O 4 /PAA system was at 7, and approximately 95% RhB could be removed within 10 min at this pH. Radical scavenging experiments indicated that organic radicals (i.e., CH 3 COO • and CH 3 COOO • ) were the dominant reactive species for RhB degradation. The X-ray photoelectron spectroscopy (XPS) analysis for the fresh and used catalysts suggested that the catalytic reaction mainly occurred on the surface of the catalyst. Increasing PAA dosage and CoFe 2 O 4 dosage could enhance the removal of RhB, while excess CoFe 2 O 4 dosage inhibited its degradation probably due to the clumping effect of magnetic nanoparticles . Five degradation products of RhB by CoFe 2 O 4 /PAA were identified and two degradation pathways of RhB were subsequently proposed, including bond cleavage and hydroxylation . CoFe 2 O 4 exhibited an excellent stability and reusability , and the removal rate of RhB could maintain at 92.4% after four cycles. Several kinds of organic contaminants were selected to evaluate the applicability of CoFe 2 O 4 /PAA system, and the results suggested that CoFe 2 O 4 /PAA system exhibited a selectivity for different contaminants.
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