The promotional mechanism of Ce substituted A-site cation over YMn2O5 for toluene oxidation

被引:1
|
作者
Meng, Fanyu [1 ,3 ]
Lai, Yijuan [1 ]
Ding, Yu [1 ]
Jia, Yong [1 ]
Zhang, Shule [2 ]
Guo, Haiwei [3 ,4 ]
机构
[1] Anhui Univ Technol, Sch Energy & Environm, Maanshan 243002, Peoples R China
[2] Nanjing Univ Sci & Technol, Sch Chem & Chem Engn, Nanjing 210094, Peoples R China
[3] Sunpower Technol Jiangsu Co Ltd, Nanjing 211112, Peoples R China
[4] Jiangsu Sunpower Heat Exchanger & Pressure Vessel, Nanjing 211112, Peoples R China
来源
MOLECULAR CATALYSIS | 2024年 / 567卷
关键词
Ce substitution; Toluene oxidation; Promotional mechanism; ENHANCED CATALYTIC-OXIDATION; LATTICE OXYGEN; PERFORMANCE; SELECTIVITY; OXIDES; METAL;
D O I
10.1016/j.mcat.2024.114447
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mullite-type YMn2O5 oxides have considerable potential for the removal of VOCs due to the abundance of lattice oxygen and the stability. The present study investigated the promotional mechanism of toluene oxidation by Asite cations of YMn2O5 with Ce. Y1-xCexMn2O5 was synthetized by sol-gel method and characterized with various techniques. The results revealed that samples doping with Ce could notably enhanced the toluene oxidation performance, and the toluene conversion of Y0.97Ce0.03Mn2O5 was 32% higher than that of YMn2O5 at 300 degree celsius. Detailed characterizations demonstrated that the modification of Ce produced an interface between YMn2O5 and YMnO3, the strong interactions at the interface improved the content of Mn3+ and oxygen vacancies, which promoted the toluene oxidation performance. Furthermore, the intermediate of toluene oxidation on Y0.97Ce0.03Mn2O5 was performed by in-situ DRIFTS. Toluene was sequentially oxidized to benzaldehyde, benzoic acid and maleic anhydride, ultimately produced H2O and CO2. This work offered a material science basis for the development of manganese-based mullite in thermal catalytic oxidation of toluene.
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页数:9
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