催化作用
1,2-二氯乙烷
水溶液
空间速度
化学
吸附
二氯乙烷
无机化学
离解(化学)
氧气
选择性
有机化学
作者
Hao Zhang,Xiaohui Gao,Binwei Gong,Shijie Shao,Chensheng Tu,Jun Pan,Yangyang Wang,Qiguang Dai,Yanglong Guo,Xingyi Wang
标识
DOI:10.1016/j.apcatb.2022.121240
摘要
MoOx/CeO2 catalysts prepared by impregnation with (NH4)6H8Mo7O28 aqueous solution were applied for catalytic oxidation of 1,2-dichloroethane. MoOx exists on CeO2 fluorite as isolated (O=)2Mo(O-Ce)2, poly MoO4 and nano-particles, of which (O=)2Mo(O-Ce)2 presents high acidity and reducibility of Mo, and decreases the basicity of CeO2, leading to the formation of reactive intermediate during 1,2-dichloroethane adsorption. The activity of MoOx/CeO2 catalysts for 1,2-dichloroethane oxidation increases with acidity and surface oxygen from CeO2 domain. The catalyst with 2.6 Mo atom nm−2 presents the highest apparent activity with T90 of 280 °C in feed containing 1000/2000 ppm 1,2-dichloroethane at 60,000 h−1 space velocity. For chlorinated aromatic oxidation, similar high stable activity is observed. The ability of (O=)2Mo(O-Ce)2 for water dissociation promotes Cl removal, and thus, the chlorination is inhibited completely within experiment temperature. Mo6+=O of (O=)2Mo(O-Ce)2 is highly stable in wet feed, leading to high resistance of MoOx/CeO2 catalysts to water.
科研通智能强力驱动
Strongly Powered by AbleSci AI