Abstract
Dry reforming of methane represents a promising approach for the valorization of CO₂ captured from industrial emissions via a high-temperature catalytic process. To this aim, a LaMn1-xNixO3 catalyst with a perovskite structure (x=0.25) for dry reforming was obtained as ultrafine powder by solution combustion synthesis and then softly deposited over -alumina supports as structured catalyst. X-ray diffraction proved that the fresh catalyst exhibits the characteristic framework of corner-sharing BO6 oc-tahedra and Mn substitution in B site. Temperature programmed reduction in H2 showed two main peaks between 200 and 400 °C and between 700 and 900 °C, proving the strong reduction of Mn oxides in different oxidation states and Ni oxide even to the elemental state. Raman spectroscopy on fresh and spent catalyst showed that carbon deposition during reforming was negligible and lattice distortion occurred associated to oxygen vacancies or partial reduction. A 25-hour reforming test with LaMn1-xNixO3 proved conversion of CH4 equal to 75% at 700°C. Dry reforming tests with the struc-tured catalyst confirmed the results obtained with the catalyst powder on a larger scale and different conditions, such as temperature, residence time and CH4/CO2 feed ratio, achieving CH4 conversion of up to 94% at 800 °C.

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