Ambient Carbon-Neutral Ammonia Generation via a Cyclic Microwave Plasma Process

A novel reactor methodology was developed for chemical looping ammonia synthesis processes using microwave plasma for pre-activation of the stable dinitrogen molecule before reaching the catalyst surface. Microwave plasma-enhanced reactions benefit from higher production of activated species, modularity, quick startup, and lower voltage input than competing plasma-catalysis technologies. Simple, economical, and environmentally benign metallic iron catalysts were used in a cyclical atmospheric pressure synthesis of ammonia. Rates of up to 420.9 mu mol min-1 g-1 were observed under mild nitriding conditions. Reaction studies showed that both surface mediated and bulk-mediated reaction domains were found to exist depending on the time under plasma treatment. The associated density functional theory (DFT) calculations indicated that a higher temperature promoted more nitrogen species in the bulk of iron catalysts but the equilibrium limited the nitrogen converion to ammonia, and vice versa. Generation of vibrationally active N2 and, N2+ ions is associated with lower bulk nitridation temperatures and increased nitrogen contents versus thermal-only systems. Additionally, the kinetics of other transition metal chemical looping ammonia synthesis catalysts (Mn and CoMo) were evaluated by high-resolution time-on-stream kinetic analysis and optical plasma characterization. This study sheds new light on phenomena arising in transient nitrogen storage, kinetics, effect of plasma treatment, apparent activation energies, and rate-limiting reaction steps.

Automated summary

A novel reactor methodology was developed for chemical looping ammonia synthesis using microwave plasma for pre-activation of dinitrogen. The reactions benefit from higher production of activated species, modularity, quick startup, and lower voltage input. Simple, economical, and environmentally benign metallic iron catalysts were used, and both surface mediated and bulk-mediated reaction domains were found to exist. Transition metal catalysts and their kinetics were also evaluated.