Dry reforming of methane with CO2 over Co-La1_xCaxNiO3 perovskite-type oxides supported on ZrO2

Under methane dry reforming conditions, Co has an impact on the stability and activity of Co-La1_xCaxNiO3-ZrO2 catalyst. In the course of the reduction reactions of perovskite precursors, the catalytic performance of Co-based bimetallic catalyst was evaluated. TEM, BET, H2-TPR, TGA, NH3-TPD, XRD and CO2-TPD techniques were used to characterize the catalyst and investigate the metal-metal/metal-support interactions as well as the phase changes that occurred under the reaction conditions. The catalyst with the highest activity was the 2%Co- La0.2Ca0.8NiO3- ZrO2due to the synergistic interaction between Ni (in the perovskite) and Co. Thus, the inclusion of Co in the catalyst, promoted the removal of carbonaceous deposits from its surrounding active sites, which in turn improved the catalyst's activity and stability. The synergistic effects of Ni-Co in the catalyst's lattice, enhanced the catalyst's performance as well as reduced the formation of carbon. Therefore, the 2%Co-La0.2Ca0.8NiO3-ZrO2 exhibited the most excellent catalyst stability, activity and the mildest carbon deposition with high CO2 and CH4 conversions of 90% and 88% respectively.

Automated summary

Co has an impact on the stability and activity of the Co-La1_xCaxNiO3-ZrO2 catalyst under methane dry reforming conditions. The catalytic performance of the Co-based bimetallic catalyst was evaluated during the reduction reactions of perovskite precursors. Various characterization techniques were used to study the metal-metal/metal-support interactions and phase changes that occurred under the reaction conditions. The 2%Co-La0.2Ca0.8NiO3-ZrO2 catalyst showed the highest activity and demonstrated excellent stability, with high CO2 and CH4 conversions of 90% and 88% respectively, attributed to the synergistic interaction between Ni and Co in the catalyst's lattice.