Ferrous ions promoted aerobic simazine degradation with Fe@Fe2O3 core-shell nanowires

被引:104
作者
Liu, Wei [1 ]
Ai, Zhihui [1 ]
Cao, Menghua [1 ]
Zhang, Lizhi [1 ]
机构
[1] Cent China Normal Univ, Key Lab Pesticide & Chem Biol, Minist Educ, Inst Environm Chem,Coll Chem, Wuhan 430079, Peoples R China
基金
美国国家科学基金会;
关键词
Fe@Fe2O3 nanowires; Molecular oxygen activation; Surface bound ferrous ions; Surface hydroxyl radicals; Simazine; ZERO-VALENT IRON; SPIN-FORBIDDEN TRANSITIONS; MOLECULAR-OXYGEN; FENTON SYSTEM; REAGENT; EFFICIENT; ACTIVATION; PESTICIDES; OXIDATION; REMOVAL;
D O I
10.1016/j.apcatb.2013.11.034
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, we investigated the effect of extra ferrous ions on the aerobic simazine degradation with Fe@Fe2O3 core-shell nanowires at circumneutral pH and interestingly found that ferrous ions could promote the aerobic simazine degradation efficiency of nanowires by about 5 times. The aerobic simazine degradation improvement was realized by maintaining enough dissolved ferrous ions and enhancing single-electron reduction molecular oxygen activation via providing more surface bound ferrous ions on the iron oxide shell. These increased surface bound ferrous ions could produce more surface hydroxyl radicals to enhance the simazine degradation. The 2,2'-bipytridine inhibition and reactive oxygen species detection results revealed that the contribution of sequential single-electron molecular oxygen activation by surface bound ferrous ions to reactive oxygen species production was more than 60%, higher than that of two-electron molecular oxygen activation pathway. We determined the degradation intermediates of simazine with high performance liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry to tentatively propose a possible simazine degradation pathway. These interesting findings could provide new insight on nanoscale zero valent iron induced molecular oxygen activation and its aerobic removal of organic pollutants at circumneutral pH. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 11
页数:11
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