Pd supported on defective TiO2 polymorphic mixtures: Effect of metal-support interactions upon glycerol selective oxidation

Palladium catalysts supported on defective mixes of anatase, TiO2 (II) and rutile crystalline phases, previously obtained by high-energy ball milling, were synthesized and tested for glycerol selective oxidation. A deep characterization of these unusual materials was carried out to elucidate catalytic and physicochemical features. Electron density transfer from support to metal or vice versa, depending on the polymorphs present, could not only alter palladium particle sizes and its surface oxidation state but also reducibility and oxygen mobility of catalysts. Furthermore, acid-base properties achieved also influenced catalytic activity under mild conditions of liquid-phase glycerol oxidation. A conversion of 94% and a selectivity to glyceric and lactic acids of 48% and 22% respectively were obtained for the Pd catalyst supported on mechanochemically activated anatase. The presence of several polymorphs in a metal oxide support could therefore benefit or handicap catalytic cycle for a particular reaction. Metal-support interactions play a key role in heterogenous catalysts and thus the rational design of supports comes on the scene.

Automated summary

Palladium catalysts supported on defective mixes of anatase and rutile phases of titanium dioxide show excellent performance in the selective oxidation of glycerol. The physicochemical features of the support material play a crucial role in determining the catalytic activity, including the particle size, surface oxidation state, reducibility, oxygen mobility, and acid-base properties. This research is important for the rational design of heterogeneous catalysts.