Improved activity and stability for chlorobenzene oxidation over ternary Cu-Mn-O-Ce solid solution supported on cordierite

被引:4
|
作者
Gu, Mingyang [1 ]
Huang, Qiong [1 ]
Xu, Lirui [1 ]
Zhu, Jie [1 ]
Sun, Yueyin [1 ]
Tao, Tao [1 ]
Yang, Bo [1 ]
Chen, Mindong [1 ]
Yang, Hong [2 ]
机构
[1] Nanjing Univ Informat Sci & Technol, Jiangsu Collaborat Innovat Ctr Atmospher Environm, Sch Environm Sci & Engn, Jiangsu Key Lab Atmospher Environm Monitoring & Po, 219 Ningliu Rd, Nanjing 210044, Peoples R China
[2] Univ Reading, Dept Geog & Environm Sci, Reading RG6 6AB, England
基金
中国国家自然科学基金;
关键词
Catalytic oxidation; Chlorinated volatile organic compound; CeO2; Cordierite; CATALYTIC COMBUSTION; ORGANIC-COMPOUNDS; PERFORMANCE; REMOVAL; MECHANISM;
D O I
10.1007/s11356-022-24988-1
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A series of CuMnOx/CeO2/cordierite and CuMnCeOx/cordierite catalysts prepared by a complex method with citric acid were investigated for the performance of chlorobenzene (CB) oxidation. The effects of the molar ratio of Mn/Cu, transition metal oxide loading, calcination temperature and time were investigated as the main investigation factor for the performance. Meanwhile, XRD, SEM, BET, H-2-TPR, O-2-TPD and XPS were conducted to characterize the physicochemical properties of these catalysts. The results demonstrated that CuMnOx/CeO2/cordierite catalysts prepared by step-by-step synthesis with the Cu/Mn molar ratio of 5:2 exhibited a high activity (T-90 = 350 ?), owing to the incorporation of CuO and MnOx for forming CuMn2O4 spinel oxide supported on CeO2 surface. More importantly, CuMnCeOx/cordierite catalysts prepared by one-step exhibited the highest oxidation activity (T-90 < 300 ?) attributed to the low H-2 reduction temperature and desorption energy of surface oxygen, and the formed Cu-Mn-O-Ce solid solution and CeO2 promoted the high dispersion of CuMnOx in the supported catalysts. In addition, the possible oxidation mechanism was described to demonstrate the by-products generation and oxygen transfer of CuMnCeOx catalysts.
引用
收藏
页码:37535 / 37546
页数:12
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