(104b) Microwave-Assisted, Performance-Advantaged Direct Propane Dehydrogenation | AIChE

(104b) Microwave-Assisted, Performance-Advantaged Direct Propane Dehydrogenation

Authors 

Wang, C., University of Delware
Ajit, K. C., Indian Institute of Technology
Yu, K., University of Delaware
Mallada, R., University of Zaragoza
Santamaria, J., University of Zaragoza
Selvam, E., University of Delaware
Julian, I., University of Zaragoza
Catala-Civera, J. M., Instituto de Tecnologías de la Información y las Comunicaciones (ITACA)
Zheng, W., University of Delaware
Vlachos, D., University of Delaware - Catalysis Center For Ener
Goyal, H., Indian Institute of Technology Madras
Non-oxidative propane dehydrogenation (PDH) produces on-site propylene, a valuable chemical feedstock. Although widely used, its efficiency is limited due to moderate selectivity and significant catalyst deactivation, which makes it operate at lower-than-ideal temperatures. This results in high energy consumption and significant pollution in the chemical industry. We demonstrate that employing microwave (MW) heating with PtSn/SiO2 catalyst pellets in a SiC monolith, acting as a MW susceptor and heat distributor, can enhance the process while maintaining conditions comparable to traditional reactors. Continuous tests show that the MW reactor remains active and stable at 500°C without the co-feeding hydrogen. At higher temperatures, feed concentrations, and with increased space velocity, MW-heated catalysts exhibit remarkable coke resistance, high activity, and exceptional selectivity, unlike conventionally heated reactors that suffer from severe deactivation. Gas-solid temperature gradients are investigated computationally, and nanoscale temperature discrepancies help elucidate the distinct coke formation mechanisms between the heating methods. This strategy highlights the immense potential of electrifying catalytic reactions for eco-friendly chemical production.