4.6 Article

Enhanced Catalytic Performance of Fe-containing HZSM-5 for Ethane Non-Oxidative Dehydrogenation via Hydrothermal Post-Treatment

期刊

CHEMCATCHEM
卷 13, 期 18, 页码 4019-4028

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.202100752

关键词

Ethane dehydrogenation; Fe; ZSM-5; hydrothermal post-treatment; highly dispersed Fe

资金

  1. National Natural Science Foundation of China [U19B2003, 21902027, 21902029]
  2. Foundation of State Key Laboratory of High-Efficiency Utilization of Coal and Green Chemical Engineering [2019-KF-23]
  3. Natural Science Foundation of Fujian Province [2020 J01443, 2020 J05121]
  4. Educational Committee of Fujian Province [JAT200042]
  5. Fuzhou University Testing Fund of precious apparatus [2021T006]

向作者/读者索取更多资源

The facile strategy of constructing Fe supported ZSM-5 (Fe/HZ5-HTS) through hydrothermal post-treatment shows superior catalytic activity and long-term stability in ethane non-oxidative dehydrogenation. The better catalytic performance is attributed to the more dispersed and exposed Fe species acting as active sites.
A facile strategy is applied to construct Fe supported ZSM-5 (Fe/HZ5-HTS) via hydrothermal post-treatment and applied to ethane non-oxidative dehydrogenation. Compared with Fe/HZ5-IWI prepared by incipient wetness impregnation, Fe/HZ5-HTS exhibits superior catalytic activity and long catalyst stability with 6000 minutes time-on-stream. An obvious volcanic curve is observed between the ethylene generation rate and Fe content, and 1.0Fe/HZ5-HTS exhibits the highest ethylene generation rate with 0.166 mmol C2H4 s(-1) g(Fe)(-1) over different Fe loading, which is twice as much as that of 1.0Fe/HZ5-IWI. According to various characterizations, isolated Fe3+ species and carburized Fe species are active sites, and the better catalytic performance over 1.0Fe/HZ5-HTS is ascribed to more disperse Fe species and exposing more Fe species in the surface. Besides, the lower ethylene desorption temperature and higher ethane desorption temperature over Fe/HZ5-HTS could suppress the overreaction of the ethylene to generate coke and increase ethane residence reaction time, resulting in less coke deposition and facilitating the catalytic performance.

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