Perovskite-type oxide catalysts for low temperature, anaerobic catalytic partial oxidation of methane to syngas

The cyclic reaction between CH4 and O2 over perovskite-type La0.8Sr0.2Fe0.8Co0.2O3−δ, La0.75Sr0.25Fe0.6Co0.15Al0.25O3−δ and La0.8Sr0.2Fe0.8Co0.2O3−δ/γ-AlO(OH), impregnated with 0.5 wt% Rh or Pt, was studied at 873 K. Synchrotron X-ray and neutron diffraction patterns of La0.75Sr0.25Fe0.6Co0.15Al0.25O3−δ proved a rhombohedral structure with Al distributed over the octahedral B-site. The oxygen non-stoichiometry (δ) was determined by thermogravimetric analysis at 958 K for pO2 > 10−22 atm. High selectivity to the partial oxidation products CO and H2 was observed when 3 − δ was lower than 2.76 and 2.78 for the mentioned oxides, with and without Al, respectively. The role of Rh relates solely to the activation of CH4. A stable high selectivity throughout the pulse sequence was achieved when utilizing partially reduced materials. In situ synchrotron XRD proved that the oxides retained the perovskite structure during the reduction/oxidation cycle, and no phase decomposition occurred. The strong correlation between results from catalytic transient tests and thermogravimetric analysis suggests that the CO selectivity is ruled by the redox potential of the reducible oxide.

The conversion of CH4 to CO and H2 by the framework oxygen of perovskite oxides promoted with Rhodium was studied at 873 K. A correlation between selectivity and redox properties of the oxides was observed, suggesting a thermodynamic dependency of the products profile.Figure optionsDownload high-quality image (79 K)Download as PowerPoint slide