Abstract
AbstractThe Cannizzaro reaction of pyruvaldehyde to lactic acid is investigated in a flow reactor with ZrO2 catalysts with different structures and acid–base properties. The results show that a difference in the crystalline structures of two ZrO2 polymorphs strongly affects the conversion of pyruvaldehyde. The monoclinic phase of zirconia is the most active for this reaction. A good correlation is observed between the reaction rate and the concentration of Lewis acid sites of sufficient strength, which shows that these sites play a major role in the reaction. A reaction mechanism is proposed involving coordinatively unsaturated Zr4+ cations as sites for activating pyruvaldehyde molecules, whereas Zr4+−O2− pairs generate terminal OH groups through water dissociation.
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