化学
催化作用
激进的
羟基自由基
分解
大肠杆菌
光化学
电子顺磁共振
核化学
无机化学
钼
硫化物
有机化学
生物化学
物理
基因
核磁共振
作者
Jun Liu,Chencheng Dong,Yuanxin Deng,Jiahui Ji,Shenyuan Bao,Cuirong Chen,Bin Shen,Jinlong Zhang,Mingyang Xing
出处
期刊:Water Research
[Elsevier BV]
日期:2018-08-20
卷期号:145: 312-320
被引量:253
标识
DOI:10.1016/j.watres.2018.08.039
摘要
Abstract As a typical advanced oxidation technology, the Fenton reaction has been employed for the disinfection, owing to the strong oxidizability of hydroxyl radicals (·OH). However, the conventional Fenton system always exhibits a low H2O2 decomposition efficiency, leading to a low production yield of ·OH, which makes the disinfection effect unsatisfactory. Herein, we develop a molybdenum sulfide (MoS2) co-catalytic Fenton reaction for rapid and highly efficient inactivation of Escherichia coli K-12 (E. coli) and Staphylococcus aureus (S. aureus). As a co-catalyst in the Fe(II)/H2O2 Fenton system, MoS2 can greatly facilitate the Fe(III)/Fe(II) cycle reaction by the exposed Mo4+ active sites, which significantly improves the H2O2 decomposition efficiency for the ·OH production. As a result, the MoS2 co-catalytic Fenton system can reach up to 83.37% of inactivation rate of E. coli just in 1 min and 100% of inactivation rate within 30 min, which increased by 2.5 times than that of the conventional Fenton reaction. Furthermore, the ·OH as the primary reactive oxygen species (ROS) in MoS2 co-catalytic Fenton reaction was measured and verified by electron paramagnetic resonance (EPR) and photoluminescence (PL). It is demonstrated an increased amount of ·OH generated from the decomposition of H2O2 in the presence of MoS2, which is responsible for the rapid and efficient inactivation of E. coli and S. aureus. This study provides a new perspective for rapid and highly efficient inactivation of bacteria in environmental remediation.
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