High Catalytic Activity in CO Oxidation over MnOx Nanocrystals

Manganese oxides of various stoichiometry were prepared via Mn-oxalate precipitation followed by thermal decomposition in the presence of oxygen. A nonstoichiometric manganese oxide, MnOx (x = 1.61…1.67) was obtained by annealing at 633 K and demonstrated superior CO oxidation activity, i.e. full CO conversion at room temperature and below. The activity gradually decreased with time-on-stream of the reactants but could be easily recovered by heating at 633 K in the presence of oxygen. CO oxidation over MnOx in the absence of oxygen proved to be possible with reduced rates and demonstrated a Mars—van Krevelen—type mechanism to be in operation. A TEM structural analysis showed the MnOx phase to form microrods with large aspect ratio which broke up into nanocrystalline manganese oxide (MnOx) particles with diameters below 3 nm and a BET specific surface area of 525 m2/g. Annealing at 798 K rather than 633 K produced well crystalline Mn2O3 which showed lower CO oxidation activity, i.e. 100% CO conversion at 335 K. The catalytic performance in CO oxidation of various Mn-oxides either studied in this work or elsewhere was compared on the basis of specific reaction rates.