(338d) Microwave Enhanced CO2 Dehydrogenation of Ethane over Supported Transition Metal Carbides | AIChE

(338d) Microwave Enhanced CO2 Dehydrogenation of Ethane over Supported Transition Metal Carbides

Authors 

Robinson, B. - Presenter, West Virginia University
Hu, J., West Virginia University
Caiola, A., West Virginia University
Brown, S., West Virginia University
CO2 dehydrogenation of ethane (CO2-DHE) over supported transition metal carbide (TMCs) catalysts consisting of molybdenum, iron, and cobalt were studied under thermal or microwave heating. Mo, Fe, and/or Co metals were loaded onto TiC, TiOx, and CeOx by wet impregnation method followed by carburization at 700oC in a 10/90 CH4/H2 atmosphere to form the transition metal carbides, located on the surface of the support materials. Different metal loadings were investigated to illustrate the support/metal effects on catalytic activity and dielectric properties. The different supports, CeOx, TiOx, and TiC were tested to determine the effect of the microwave on different supports. The CeOx is a commonly used/well-studied support that is often regarded for its Ce3+ and Ce4+ reactivity. Whereas, TiOx is less commonly used, but shows promising aspects as a photocatalyst due to its semiconductor properties. Generally, TiOx has an n-type semiconductor response, however, modification by metal doping often results in the more desired p-type semiconductor response. TiC is a less studied support for the CO2 ethane dehydrogenation reaction but is a very good microwave absorber that exhibits good chemical stability and electrical conductivity.

Microwave heating was carried out in a 900-watt 2.45GHz solid-state microwave equipped with automatic tunning, pyrometer temperature measurement, and PID temperature control. A thermal imager was used to extract temperature distributions profiles of the catalyst beds. Thermal heating was carried out in a resistively heated tubular furnace controlled by PID. TPR, BET, TGA, XRD, Raman, and TEM were used to characterize the samples before and after the CO2-DHE reaction. It was found that the microwave produced different effects based on the type of support. For the TiC supported samples exhibited higher microwave absorption and lower power requirements than TiOx or CeOx. The lower power requirements resulted in a higher ethylene/g-cat/watt ratio than that produced for the TiOx supported samples. Thus, suggesting that the TiC is a more suitable catalyst support for microwave heating than the conventional TiOx. This work draws attention to the importance of catalyst design for microwave enhanced reactions.