Solvent Effects on the Hydrodeoxygenation of Propanoic Acid over Pd (111) Model Surfaces
Engineering, Chemical Engineering, Catalysis and Reaction Engineering, Organic Chemistry
The effects of liquid water, n-octane, and n-butanol on the hydrodeoxygenation of propanoic acid over Pd(111) model surfaces have been studied from first principles. We developed a microkinetic model for the hydrodeoxygenation and studied the reaction mechanism at a temperature of 473 K. Our model predicts that for all reaction media, decarbonylation pathways are favored over decarboxylation pathways. However, in the presence of polar solvents like water, decarboxylation routes become competitive with decarbonylation routes. The activity of the Pd surface varies as a function of the environment as follows: water > n-butanol > octane ≈ gas phase. Finally, a sensitivity analysis of our models suggests that both C–OH and C–H bond cleavages control the overall rate of the catalyst in all environments and are likely to be activity descriptors for the hydrodeoxygenation of organic acids.
Published in Green Chemistry, Volume 16, Issue 2, 2013, pages 605-616.
© Green Chemistry, 2014, Royal Society of Chemistry
Behtash, S., Lu, J., Faheem, M., Heyden, A. (2014). Solvent Effects on the Hydrodeoxygenation of Propanoic Acid over Pd (111) Model Surfaces. Green Chemistry, 16(2), 605-616.