氯
催化作用
乙烯
化学
选择性
环氧乙烷
反应性(心理学)
无机化学
反应速率常数
动力学
化学动力学
多相催化
有机化学
物理
医学
病理
聚合物
替代医学
量子力学
共聚物
作者
K. R. Krishna Iyer,Aditya Bhan
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2021-11-29
卷期号:11 (24): 14864-14876
被引量:26
标识
DOI:10.1021/acscatal.1c03493
摘要
Ethylene epoxidation transpires with high ethylene oxide (EO) selectivity (∼90%) over promoted Ag/α-Al 2 O 3 catalysts via the concurrent propagation of ethylene oxidation, chlorine deposition and removal, and EO degradation catalytic cycles with reactant and product species (C 2 H 4, O 2, CO 2 ) involved in multiple reaction pathways. We resolve the interdependent kinetics of ethylene oxidation and chlorine deposition and removal catalytic cycles by measuring EO synthesis rates at constant chlorine coverages. The systematic variation in ethylene and oxygen reaction orders for ethylene epoxidation with chlorine coverage illustrates how organochloride promoters impact the kinetics of EO synthesis. EO degradation kinetics measured over promoted α-Al 2 O 3 materials are not influenced by the chlorine promoter; however, EO degradation rates over α-Al 2 O 3 can be as high as 3% of total EO formation rates and can contribute perceptibly to lowering net EO selectivity. We develop a reactor model that incorporates the kinetic interdependencies among the three catalytic sequences in terms of discernible changes in reaction orders for EO formation, chlorine coverage, and EO degradation rates across a packed bed and such a description, in turn, enables accurate predictions of the EO rate and selectivity over a wide range of process conditions.
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