Abstract

Chemical looping reforming with CO2 splitting (CLRS) is an attractive process that can be used for conversion of hydrocarbons into syngas, an industrially important intermediate that serves as a building block for other value-added products. Under the chemical looping approach, the oxygen carrier that provides lattice oxygen, instead of molecular oxygen, is used for methane partial oxidation. This work focuses on MgO-supported Ca2Fe2O5 redox materials as the oxygen carriers for simultaneous syngas production and CO2 utilization through thermochemical CO2 splitting using a two-reactor chemical looping system. We experimentally achieve a near 100% CH4 conversion and a high syngas selectivity of >98%, which is by far the highest in chemical looping reforming systems. Complete regeneration of the reduced oxygen carriers is obtained using CO2 with ~78% conversion, thereby operating close to the thermodynamic limit. Density functional theory calculations reveal that the lattice oxygen in corner-sharing octahedra of brownmillerite structure possessed by Ca2Fe2O5 acts as the efficient active sites for CO and H2 production. The formed oxygen vacancy significantly reduces the energy barriers of C-H cleavage and CO formation, leading to the reactivity and selectivity enhancement. MgO assists in reactivity enhancement by enabling higher degree of Ca2Fe2O5 dispersion along with increasing Ca2Fe2O5′s tolerance towards sintering. These findings will contribute to the systematic design of high-performance redox materials and chemical looping processes for syngas production with CO2 utilization.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call