Enhancement of H2O2 Decomposition by the Co-catalytic Effect of WS2 on the Fenton Reaction for the Synchronous Reduction of Cr(VI) and Remediation of Phenol

被引:359
作者
Dong, Chencheng
Ji, Jiahui
Shen, Bin
Xing, Mingyang [1 ]
Zhang, Jinlong [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Key Lab Adv Mat, 130 Meilong Rd, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
WASTE-WATER TREATMENT; LIGHT PHOTOCATALYTIC DEGRADATION; GRAPHENE OXIDE; CARBON NANOTUBES; METHYLENE-BLUE; ADSORPTIVE DEGRADATION; ORGANIC POLLUTANTS; ACTIVATED CARBON; REMOVAL; DYE;
D O I
10.1021/acs.est.8b02403
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The greatest problem in the Fe(II)/H2O2 Fenton reaction is the low production of center dot OH owing to the inefficient Fe(III)/Fe(II) cycle and the low decomposition efficiency of H2O2 (<30%). Herein, we report a new discovery regarding the significant co-catalytic effect of WS2 on the decomposition of H2O2 in a photoassisted Fe(II)/H2O2 Fenton system. With the help of WS2 co-catalytic effect, the H2O2 decomposition efficiency can be increased from 22.9% to 60.1%, such that minimal concentrations of H2O2 (0.4 mmol/L) and Fe2+ (0.14 mmol/L) are necessary for the standard Fenton reaction. Interestingly, the co-catalytic Fenton strategy can be applied to the simultaneous oxidation of phenol (10 mg/L) and reduction of Cr(VI) (40 mg/L), and the corresponding degradation and reduction rates can reach up to 80.9% and 90.9%, respectively, which are much higher than the conventional Fenton reaction (52.0% and 31.0%). We found that the expose reductive W4+ active sites on the surface of WS2 can greatly accelerate the rate-limiting step of Fe3+/Fe2+ conversion, which plays the key role in the decomposition of H2O2 and the reduction of Cr(VI). Our discovery represents a breakthrough in the field of inorganic catalyzing AOPs and greatly advances the practical utility of this method for environmental applications.
引用
收藏
页码:11297 / 11308
页数:12
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