Influence of the Thermal Processing and Doping on LaMnO3 and La0.8A0.2MnO3 (A = Ca, Sr, Ba) Perovskites Prepared by Auto-Combustion for Removal of VOCs

Single-phase oxygen stoichiometric LaMnO3 and doped La(0.8)A(0.2)MnO(3) (A = Ca, Sr, Ba) perovskites have been prepared by a simple one-step auto-combustion method. Cation-deficient LaMnO3+delta and La(0.8)A(0.2)MnO(3+delta) were obtained by calcination of the former samples in air at 750 degrees C. The samples were characterized by X-ray powder diffraction, X-ray photoelectron spectroscopy, temperature-programmed reduction, temperature-programmed oxygen desorption, and N-2 physisorption in order to apply them as catalysts in the complete catalytic oxidation of acetone as a model volatile organic compound. The studied phases show the expected orthorhombic and rhombohedral perovskite crystal structures. Catalytic experiments performed with all the samples show measurable activity already at 100 degrees C. At 200 degrees C, doped La(0.8)A(0.2)MnO(3) samples show higher activity than undoped LaMnO3, with increasing conversion with larger A-cation size. Calcined samples also show higher activity than as-prepared ones making La0.8Ba0.2MnO3+delta the best catalyst at this temperature. All doped samples show >95% acetone conversion at T >= 250 degrees C with a weak dependence on the sample processing or A cation doping. The collected evidence confirms that the most important factors for the catalytic activity of these oxides are the Mn4+/Mn3+ molar ratio on the surface of the samples and the cation-deficiency of the bulk perovskite structure. In addition, increasing the symmetry of the bulk crystal structure appears to have an additional favourable effect. Despite the observation of the presence of surface carbonates, we show that it is possible to use the as-prepared samples without further thermal treatment with good results in the oxidation of acetone.

Automated summary

Single-phase oxygen stoichiometric LaMnO3 and doped La(0.8)A(0.2)MnO(3) (A = Ca, Sr, Ba) perovskites were prepared by a simple one-step auto-combustion method. Cation-deficient LaMnO3+delta and La(0.8)A(0.2)MnO(3+delta) were obtained by calcination of the former samples in air at 750 degrees C. The catalytic activity of these oxides is influenced by the Mn4+/Mn3+ molar ratio on the surface of the samples and the cation-deficiency of the bulk perovskite structure.