CeO2 enhanced performance of NiFe2O4-CaO for carbon capture and in-situ hydrogenation conversion to CO
NiFe 2 O 4 exhibits excellent redox properties and is widely applied in CaO-NiFe 2 O 4 chemical looping processes. However, rapid sintering of Ni-Fe alloy under reaction conditions limited its industrial applications. The CeO 2 -NiFe-CaO were synthesized through a physical mixing method with NiFe 2 O 4 as a precursor, and its CO 2 capture capacity and in-situ hydrogenation performance were conducted on ICCC-RWGS reaction under different conditions. 20CeO 2 -NiFe-CaO exhibited a CO yielding of 9.35 mmol/g at 650 °C. During the carbon capture stage, CO 2 was adsorbed by CaO, leading to the formation of CaCO 3 . In the hydrogenation conversion stage, hydroxyl groups were generated on the surface, combining with CaCO 3 to produce formate species, further generating H 2 O and CO. 15CNF-CaO exhibited superior cyclic ICCC-RWGS reaction performance compared to 15NF-CaO, with a CO yield of 1.88 mmol/g after 40 cycles. CeO 2 inhibited the sintering of catalytic components, preserving a higher specific surface area and smaller particle size. Furthermore, CeO 2 in 15CNF-CaO inhibited carbon deposition and enhanced in-situ hydrogenation performance, exhibiting better CaO regeneration capability and better cyclic stability. These results could provide insight for designing the DFMs for the ICCC-RWGS process.
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