离解(化学)
催化作用
氨
等离子体
介质阻挡放电
氨生产
化学
吸附
限制
朗缪尔探针
化学工程
光化学
物理化学
离子
等离子体诊断
有机化学
电极
物理
工程类
机械工程
量子力学
作者
Kevin van ’t Veer,Yannick Engelmann,François Reniers,Annemie Bogaerts
标识
DOI:10.1021/acs.jpcc.0c05110
摘要
Plasma-catalytic ammonia synthesis is receiving ever increasing attention, especially in packed bed dielectric barrier discharge (DBD) reactors. The latter typically operate in the filamentary regime when used for gas conversion applications. While DBDs are in principle well understood and already applied in the industry, the incorporation of packing materials and catalytic surfaces considerably adds to the complexity of the plasma physics and chemistry governing the ammonia formation. We employ a plasma kinetics model to gain insights into the ammonia formation mechanisms, paying special attention to the role of filamentary microdischarges and their afterglows. During the microdischarges, the synthesized ammonia is actually decomposed, but the radicals created upon electron impact dissociation of N2 and H2 and the subsequent catalytic reactions cause a net ammonia gain in the afterglows of the microdischarges. Under our plasma conditions, electron impact dissociation of N2 in the gas phase followed by the adsorption of N atoms is identified as a rate-limiting step, instead of dissociative adsorption of N2 on the catalyst surface. Both elementary Eley–Rideal and Langmuir–Hinshelwood reaction steps can be found important in plasma-catalytic NH3 synthesis.
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