Integrated CO2 capture and conversion by Cu/CaO dual function materials: Effect of in-situ conversion on the sintering of CaO and its CO2 capture performance

Abstract

The integrated carbon capture and utilization (ICCU) technology has been considered a prospective strategy for mitigating carbon emissions issues. Compared to conventional CO2 capture and utilization, the ICCU process reduces transporting, product purification, construction, and operation costs. However, few works focus on investigating the effect of in-situ CO2 conversion on the sintering of CaO at high temperatures. In this work, Cu/CaO dual functional materials (DFMs) were synthesized and used in the Calcium Looping-Reverse Water-Gas Shift (CaL-RWGS) process at 650 °C. The results showed that it is thermodynamically feasible to couple the CaL with the RWGS reaction. In the cyclic CO2 capture test, Ca1Cu0.1 DFMs showed desirable CO2 capture performance (11.34 mmol/gDFMs) and self-activated phenomenon in the first 15 cycles. Moreover, Cu nanoparticle catalysts in the DFMs effectively inhibited the sintering of CaO by accelerating the desorption of CO2 from the CaO surface and converting it to CO during the conversion stage. In-situ DRIFTS of Ca1Cu0.1 DFMs revealed that formates might be the RWGS intermediates in CaL-RWGS.