(658c) Tuning the Hydrogenation of CO2 to CH4 over Mechano-Chemically Prepared Palladium Supported on Ceria
AIChE Annual Meeting
2023
2023 AIChE Annual Meeting
Catalysis and Reaction Engineering Division
CO2 Upgrading V: Mechanistic Insight II
Tuesday, November 7, 2023 - 8:36am to 8:54am
CO2 methanation reactivity, reaction mechanism, and surface structure were investigated on a mechanochemically prepared Pd/CeO2 catalyst (PdAcCeO2-M), where an oxidative pretreatment (-o) increased methane yield by a factor of two compared to a reductive pretreatment (-h). Methanation rates were maintained for over 48 hours and further increased upon oxidative regeneration treatments. The surface species of both PdAcCeO2-M-o and PdAcCeO2-M-h were explored via in situ CO2 and CO hydrogenation DRIFTS, where CO hydrogenation effectively models the dissociative CO2 mechanism (CO2 à CO à CH4). Additionally, isotopically labeled CO2 hydrogenation showed that bridged formate was the primary intermediate and the influence of *OH/Ovac was critical for methanation. PdAcCeO2-M-o yielded distinct Pd-CO adsorption and the absence of monodentate carbonate at ~ 1400 cm-1, while AP-XPS showed that PdAcCeO2-M-o yielded a unique Pdδ+ contribution at 335.9 eV. By gaining insights from various in-situ spectroscopic techniques, and by breaking the CO2 hydrogenation mechanism into piecewise steps, a deeper understanding of the direct CO2 reduction towards methane and CO over mechanochemically prepared Pd/CeO2 catalysts was obtained.