Affiliation:
1. Department of Materials Science and Engineering Northwestern University 2145 Sheridan Road Evanston IL 60208 United States
2. Department of Chemical and Biological Engineering Northwestern University 2145 Sheridan Road Evanston IL 60208 United States
3. Department of Chemistry Northwestern University 2145 Sheridan Road Evanston IL 60208 United States
4. Center for Catalysis and Surface Science Northwestern University 2145 Sheridan Rd. Evanston IL 60208 United States
Abstract
AbstractMethane dehydroaromatization (MDA) is one of the most promising technologies for directly transforming methane into aromatics. Unlike the extensively investigated Mo/ZSM‐5 catalysts, the structure and, consequently, the catalytic activity of Fe/ZSM‐5 are markedly influenced by the method of preparation, as shown here. In this study, we prepared 2 % and 4 % Fe/ZSM‐5 catalysts via wet impregnation (WI) and incipient wetness impregnation (IWI). Characterizations (XRD, STEM, UV‐Vis, NH3‐TPD and H2‐TPR) reveal that 2 %Fe‐WI mainly possesses isolated or low‐polymerized Fe species within zeolite channels, leading to a rapid activation and a higher benzene yield due to the faster reduction to iron suboxides under MDA conditions. In contrast, 2 %Fe‐IWI contains bulk iron oxide aggregates, resulting in a slower activation as these aggregates transform into iron carbide through successive reduction and carbonization. A deactivation kinetic study applied to the 2 % catalysts further demonstrates the quantitative relation between Fe site isolation and catalytic activity. Although both 4 % catalysts inevitably form sizable iron oxide clusters and particles due to the high Fe/Al ratio, similar trends are noted, with the WI catalysts exhibiting a shorter induction/activation period and a higher yield of benzene, paralleling observations made with 2 % catalysts.
Funder
U.S. Department of Energy
International Institute for Nanotechnology, Northwestern University
Basic Energy Sciences
Northwestern University
Dow Chemical Company