催化作用
乙烯
沸石
化学工程
焦炭
喷气燃料
化学
产量(工程)
级联
燃烧
选择性
材料科学
有机化学
色谱法
冶金
工程类
作者
Hend Omar Mohamed,Omar Abed,Naydu Zambrano,Pedro Castaño,Idoia Hita
标识
DOI:10.1021/acs.iecr.2c02303
摘要
Jet fuel production from ethylene oligomerization opens a sustainable pathway to clean sulfur-free fuel that is increasingly in demand due to the potential renewable origin of ethylene. The key to a viable heterogeneously catalyzed process is to improve the selectivity of the jet fuel while prolonging the catalyst lifetime. To this end, we have assessed and optimized a dual-bed cascade system based on a dimerization bed that is followed by an oligomerization bed using Ni supported on Y zeolite and ZSM-5 zeolite catalysts, respectively. Our optimization approach uses different catalyst acidities, temperatures, and bed configurations for determining the best yield–conversion relationship. Under optimized dual-bed conditions, we can produce 64 wt % of jet fuel at the beginning of the reaction and maintain a 50 wt % selectivity of this fraction for over 20 h on stream. This paper also analyzes coke deposition (content and nature) at the different experimental conditions and catalyst bed arrangements using temperature-programmed combustion. We demonstrate that the dual-bed approach is effective for protecting the main oligomerization bed (ZSM-5 catalyst) from deactivation, leading to the formation of a lighter type of coke compared with that using the initial Ni2+ HY-based dimerization catalyst, which deactivates at a faster rate.
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