In situ growth of nickel based catalysts on the surface of macroporous Al2O3 for CO2

Addressing the issue of sintering of the active component on the catalyst due to the strong exothermicity of CO2 methanation and the demand for reactions to operate at high space velocities, this study for the first time utilized macroporous Al2O3 for CO2 methanation reactions.

A catalyst comprising a high surface area, large pore size, and high pore volume was prepared by in-situ growth of layered double hydroxide (LDH) precursors on the surface of macroporous Al2O3. The effects of calcination temperature, reduction temperature, and space velocity on the catalyst structure and reaction performance were studied. The phase composition of the catalyst is controlled by adjusting the calcination temperature, the reduction degree of Ni is regulated and the sintering of Ni is avoided by controlling the reduction temperature , and the number of active sites of Ni0 in the reduced catalyst is increased, thus the activity of the catalyst is improved. The results demonstrate that after calcination of the NiMgAl-LDH precursor at 400 oC and reduction at 650 oC, the resulted Ni-MgO/Al2O3 showed the highest Ni activity-specific surface area, which is the best catalyst with highest CO2 conversion and CH4 selectivity, indicating that increasing the surface area of metal nickel is crucial for the catalytic performance.