4.8 Article

Non-oxidative dehydrogenation of ethane to ethylene over ZSM-5 zeolite supported iron catalysts

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 256, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2019.117816

Keywords

Non-oxidative ethane dehydrogenation; Fe/ZSM-5 catalyst; Active sites; Support effect; Iron carbide

Funding

  1. U.S. Department of Energy (USDOE), Office of Energy Efficiency and Renewable Energy (EERE), Advanced Manufacturing Office (AMO) RD Projects Emerging Research Exploration, and Idaho National Laboratory Directed Research and Development Program under DOE Id [DE-AC07-051D14517]
  2. NSF [CHE-1726332, CNS-1006860, EPS-1006860, EPS-0919443]

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The shale gas boom has stimulated tremendous interests in ethylene production using ethane as the feedstock. Catalytic non-oxidative ethane dehydrogenation (EDH) to ethylene represents a viable strategy to improve the process energy efficiency and to minimize the environmental impact. The breakthroughs in catalyst design play a key role in the successful development of this process. Herein, we demonstrate that iron supported on ZSM-5 zeolite (Fe/ZSM-5) is a highly efficient catalyst for the EDH reaction. Under comparable conditions, Fe/ZSM-5 exhibits superior activity and stability over various metal (Pt) or metal oxide catalysts (Zn, Ga, Cr, Mo) supported on ZSM-5. The use of ZSM-5 instead of conventional gamma-Al2O3 as the support for Fe catalysts is critical to achieve high activity and selectivity in the EDH reaction. Detailed structure characterizations combined with density functional calculations indicate that iron oxides in the as-prepared Fe/ZSM-5 catalysts are reduced to iron metal and then carburized under reaction condition, which accounts for the excellent activity and stability for the EDH reaction. Compared with Fe/Al2O3, the relatively weaker binding strength of ethylene and the weaker surface acidity on Fe/ZSM-5 allow facile desorption of ethylene, which suppresses its consecutive transformation into higher hydrocarbons and carbon deposits, resulting in higher ethylene selectivity.

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