Simultaneous photoinduced generation of Fe2+ and H2O2 in rivers: An indicator for photo-Fenton reaction

被引:9
|
作者
Mostofa, Khan M. G. [1 ,2 ]
Sakugawa, Hiroshi [2 ]
机构
[1] Tianjin Univ, Inst Surface Earth Syst Sci, Tianjin 300072, Peoples R China
[2] Hiroshima Univ, Grad Sch Biosphere Sci, Dept Environm Dynam & Management, Higashihiroshima 7398521, Japan
来源
JOURNAL OF ENVIRONMENTAL SCIENCES | 2016年 / 47卷
基金
日本学术振兴会;
关键词
Photo-Fenton reaction; Fe3+; Fe2+; Dissolved organic spatter; H2O2; Light; DISSOLVED ORGANIC-MATTER; HYDROXYL RADICAL FORMATION; HYDROGEN-PEROXIDE; WATER SAMPLES; IRON(II); DYNAMICS; SEAWATER; SEA;
D O I
10.1016/j.jes.2015.12.020
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The photo-Fenton reaction is a key source of the highly reactive hydroxyl radical (HO) that is produced by the reaction of simultaneous photo-induced generation of Fe2+-dissolved organic matter (DOM) with H2O2 in sunlit surface waters as well as in the treatment of organic pollutants in the advanced oxidation processes (AOPs). Concentrations of both H2O2 and Fe2+-DOM were dependent on time and total solar intensity flux, and their levels were highest in the diurnal samples collected at noon compared with the samples collected during the period before sunrise and after sunset. H2O2 and Fe2+-DOM concentrations during monthly readings were also found higher in comparison with the diurnal samples, shortly before sunrise or after sunset. A pi-electron bonding system is formed between Fe and the functional groups in DOM (Fe-DOM), through electron donation from the functional groups of DOM to an empty d-orbital of Fe. The pi-electron is loosely bound and is highly susceptible to a rapid excitation upon light exposure that will provide better understanding of the formation of aqueous electrons, superoxide radical anions, H2O2 and finally, photo-Fenton reactions, too. Our results imply that simultaneous generation of H2O2 and Fe2+-DOM upon sunlight exposure during the daytime is most likely to be the key photo-Fenton reaction pathway, taking place in surface waters. (C) 2016 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
引用
收藏
页码:34 / 38
页数:5
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