详细信息
Morphology effect of cerium dioxide on the catalytic performance of Ru/ CeO2 catalyst for the oxidation of different CVOCs ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Morphology effect of cerium dioxide on the catalytic performance of Ru/ CeO2 catalyst for the oxidation of different CVOCs
作者:Xie, Baocheng[1];Wang, Zhuopeng[1];Zhang, Xin[1];Ding, Min[1];Li, Mingqi[1];Guo, Xiaohan[1];Dai, Qiguang[1];Wang, Li[1];Zhan, Wangcheng[1];Guo, Yun[1];Wang, Aiyong[1];Guo, Yanglong[1]
机构:[1]East China Univ Sci & Technol, Res Inst Ind Catalysis, Sch Chem & Mol Engn, State Key Lab Green Chem Engn & Ind Catalysis, Shanghai 200237, Peoples R China
年份:2024
卷号:345
外文期刊名:SEPARATION AND PURIFICATION TECHNOLOGY
收录:;EI(收录号:20241515905183);WOS:【SCI-EXPANDED(收录号:WOS:001235607900001)】;
基金:This work was supported by the National Key Research and Devel- opment Program of China (2022YFB3504200) , the National Natural Science Foundation of China (22106101, U21A20326) , and the Funda- mental Research Funds for the Central Universities.
语种:英文
外文关键词:CVOCs; Catalytic oxidation; Ceria morphology; Ru
摘要:CeO2 with different morphology of rod-shape (R-CeO2), cube-shape (C-CeO2) and octahedra-shape (O-CeO2) were synthesized as supports and impregnated with Ru to obtain Ru/CeO2 catalysts, and the performance of which in catalytic oxidation of different chlorine-containing volatile organic compounds (CVOCs) (1,2dichloroethylene (DCE) and vinyl chloride (VC)) were investigated. Due to the stronger interaction between Ru and R-CeO2, Ru was highly dispersed on R-CeO2 and more Ru entered support lattice to form Ru-O-Ce structure, thus Ru/R-CeO2 catalyst exhibited better redox property. Ru addition enhanced the acidity of Ru/R-CeO2 and Ru/C-CeO2, while that of Ru/O-CeO2 decreased instead. The acidity mainly affected DCE catalytic activity when catalyst had sufficient redox property and chlorine resistance. Run+ content was the main factor affecting VC catalytic activity. Ru/R-CeO2 catalyst exhibited the best catalytic activity in both DCE and VC catalytic oxidation with T50 of 285 degrees C and 207 degrees C, respectively, due to its excellent redox property, acidity, and sufficient Run+. In situ DRIFTS suggested that DCE was first dissociated to VC and then oxidized to carboxylates, and the addition of Ru led to the oxidation of carboxylates to carbonyl and ultimately to complete oxidation to CO2 and H2O. Run+ was important for the oxidation of carboxylate intermediates.
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