分解
化学
催化作用
限制
化学分解
苯酚
降级(电信)
无机化学
核化学
氧化还原
有机化学
计算机科学
电信
机械工程
工程类
作者
Chencheng Dong,Jiahui Ji,Bin Shen,Mingyang Xing,Jinlong Zhang
标识
DOI:10.1021/acs.est.8b02403
摘要
The greatest problem in the Fe(II)/H2O2 Fenton reaction is the low production of ·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.
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