Strong Enhancement on Fenton Oxidation by Addition of Hydroxylamine to Accelerate the Ferric and Ferrous Iron Cycles

被引:457
作者
Chen, Liwei [1 ]
Ma, Jun [1 ,2 ]
Li, Xuchun [1 ]
Zhang, Jing [1 ]
Fang, Jingyun [1 ]
Guan, Yinghong [1 ]
Xie, Pengchao [1 ]
机构
[1] Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
[2] Natl Engn Res Ctr Urban Water Resource & Environm, Harbin 150090, Peoples R China
关键词
HYDROGEN-PEROXIDE; KINETICS; RADICALS; REAGENT; ACID; HYDROLYSIS; REDUCTION; MECHANISM; CONSTANT; PH;
D O I
10.1021/es2002748
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Fenton system generates reactive species with high oxidation potential such as hydroxyl radicals (HO center dot) or ferryl via the reaction between Fe (II) and H2O2. However, a number of drawbacks limit its widespread application including the accumulation of Fe (III) and the narrow pH range limits, etc. The aim of this study is to propose a much more efficient Fenton-HA system which is characterized by combining Fenton system with hydroxylamine (NH2OH), a common reducing agent, to relieve the aforementioned drawbacks, with benzoic acid (BA) as the probe reagent. The presence of NH2OH in Fenton's reagent accelerated the Fe (III)/Fe (II) redox cycles, leading to relatively steady Fe (II) recovery, thus, increased the pseudo first-order reaction rates and expanded the effective pH range up to 5.7. The HO center dot mechanism was confirmed to be dominating in the Fenton-HA system, and the generation of HO center dot was much faster and the amount of HO center dot formed was higher than that in the classical Fenton system. Furthermore, the major end products of NH2OH in Fenton-HA system were supposed to be NO3- and N2O.
引用
收藏
页码:3925 / 3930
页数:6
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