Effects of support identity and metal dispersion in supported ruthenium hydrodeoxygenation catalysts

Abstract Substituted phenols are the most recalcitrant oxygenates in conventional pyrolysis oils and the dominant oxygenates in lower-oxygen content, formate-assisted pyrolysis oils (FAsP). Ru catalysts with a wide range of dispersion on carbon, silica, alumina, and titania supports were synthesized, characterized and evaluated for hydrodeoxygenation (HDO) activity using phenol as a model compound. Metal content, phase, and particle size were determined with ICP-OES, EXAFS/XANES, and CO pulse chemisorption, respectively. High dispersion of ruthenium on the supports converts more phenol to products. The majority of catalysts predominantly catalyze the hydrogenation (HYD) route typical of noble metal catalysts. A highly dispersed Ru/TiO 2 catalyst shows unusually high selectivity toward direct deoxygenation (DDO) and outstanding activity. We suggest that the DDO pathway on titania involves a bifunctional catalyst, where hydrogen creates reduced titania sites, created by hydrogen spillover, that interact strongly with the phenol hydroxyl group.