?-Al2O3 doped with cerium to enhance electron transfer in catalytic ozonation of phenol

被引:28
|
作者
Li, Yu [1 ]
Wu, Luchao [1 ]
Wang, Yun [1 ]
Ke, Peng [1 ]
Xu, Jie [1 ]
Guan, Baohong [2 ]
机构
[1] Zhejiang Univ, Coll Environm & Resource Sci, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Key Lab Environm Remediat & Ecol Hlth, Coll Environm Resource Sci, Minist Educ, Hangzhou 310058, Peoples R China
关键词
OZONE DECOMPOSITION; SUPPORTED MANGANESE; AQUEOUS-SOLUTION; OXALIC-ACID; DEGRADATION; MECHANISM; MCM-41; OXIDATION; INSIGHT; FACETS;
D O I
10.1016/j.jwpe.2020.101313
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ozone decomposition into free radicals, which can be facilitated by enhancing electron transfer between ozone and catalyst, is an important segment in catalytic ozonation. We doped cerium uniformly on γ-Al2O3 with an impregnation–calcination method to enhance electron transfer in catalytic ozonation of phenol in aqueous solution. The removal efficiency of phenol is raised from 39.7% by ozonation alone to 46.3% by catalytic ozonation with Ce/Al2O3 in 50 min reaction. A higher Ce3+/Ce4+ ratio in Ce/Al2O3 witnesses a higher electron transfer rate in catalytic ozonation and thus a higher degradation efficiency of phenol, illustrating that the activity of Ce/Al2O3 depends on the valence state of Ce. The electron transfer cycle is formed by the electron donation from Ce3+ to ozone molecule and the electron acceptance of Ce4+ from adjacent lattice oxygen. After getting the electron, the ozone molecule is decomposed to generate free radical of ·OH on the surface of Ce/Al2O3. The continuous flow experiments exhibit a stable and high catalytic activity of Ce/Al2O3 for catalytic ozonation, implying the feasibility in practical application. © 2020 Elsevier Ltd
引用
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页数:7
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