Selective CO2 reduction to methane catalyzed by mesoporous Ru-Fe3O4/CeOx-SiO2 in a fixed bed flow reactor

• Ru 0 , Fe 3 O 4 and CeO x nanoparticles are immobilized over mesoporous silica. • Ru-Fe 3 O 4 /CeO x -SiO 2 catalyst is very efficient for the selective CO 2 reduction to methane. • Ceria promoter enhances the CO 2 conversion to CH 4 significantly. • Ru-Fe 3 O 4 /CeO x -SiO 2 catalyst exhibits high efficiency over fixed bed reactor at 575 K and 20 bar pressure. Development of a robust catalyst for selective reduction of CO 2 directly into hydrocarbon fuels is very challenging from both energy and environmental perspectives as it offers a renewable and green route for the production of fuels. Herein, we report a novel catalyst synthesized via excess solution impregnation of Ru and Fe 3 O 4 nanoparticles (NPs) on ceria promoted mesoporous silica SBA-15 support. The selective catalytic reduction of CO 2 to methane was carried out in the presence of H 2 over novel Ru-Fe 3 O 4 /CeO x -SiO 2 (Ce 3+ /Ce 4+ , x=1.64) catalyst in a fixed bed reactor. The CO 2 conversion was found to be 82% at 0.25 wt% ruthenium loading, 2.5 wt% iron loading, 575 K temperature, 20 bar pressure, 3000 mLg −1 h −1 gas hour space velocity and H 2 to CO 2 mole ratio of 5:1. The close contact between ruthenium and Fe 3 O 4 nanoparticles facilitated the reduction of CO 2 through hydrogen spill-over effect at lower temperature, whereas ceria NPs acted as a promoter for this reduction reaction. The catalysts were characterized thoroughly using physicochemical techniques such as CO chemisorption, BET, TPR, TPD, XRD, SEM, HR- TEM, ICP-AES and XPS analyses. High surface area and large mesopores of silica support facilitated the fine dispersion of the active catalytic sites and oxygen vacancy as supported from the DFT study on the catalytic activity. Optimal process conditions could render much higher CO 2 conversion efficacy for selective methane synthesis in comparison with previous investigations.