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- 2018 AIChE Annual Meeting
- Catalysis and Reaction Engineering Division
- Poster Session: Catalysis and Reaction Engineering (CRE) Division
- (544fn) Dehydroaromatization of Ethylene over Metal-ZSM-5 Catalysts
Industrial production of aromatics heavily relies on catalytic reforming in refineries.1-2 Driven by the limited supply of fossil fuels and the recent shale gas revolution, it is highly desirable to develop methane- and/or light olefin-based processes to meet the growing demand for aromatics. Ethylene dehydroaromatization (DHA) over Ag-ZSM-5 is one of the promising technologies given the availability of ethylene feedstock. Ag-ZSM-5 was chosen for the ethylene DHA reaction, in part because Ag-ZSM-5 was reported to promote aromatic selectivity in the isobutane aromatization,3 and to facilitate non-oxidative methane upgrading at moderate reaction temperatures.4 Here, we will report the influence of Ag species in Ag-ZSM-5 on ethylene DHA without and with co-feeding methane. We observe that Ag-ZSM-5 greatly promotes aromatic selectivities by ~3-fold. In contrast, H-ZSM-5 tends to produce light olefins and other aliphatic hydrocarbons under otherwise identical conditions.5 With methane co-feed, Ag- and H-ZSM-5 both exhibit very similar catalytic behavior compared to the conditions without methane. Interestingly, methane is activated over Ag-ZSM-5 (⤠5% conversion), but H-ZSM-5 is inactive for methane conversion.
Through systematic studies of Ag/H-ZSM-5 by a combination of experiments and density functional theory calculations at different reaction conditions, we have been able to differentiate the role of Ag species in methane/ethylene activation with enhanced product selectivities to value-added aromatics. We have also extended this study to several metals in an attempt to establish more robust structure-performance relationships in DHA catalysis. Collectively, this work provides new insights into the design of metal-containing zeolite catalysts for natural gas upgrading.