Abstract
The chemical looping reverse water gas shift (CL-RWGS) catalytic process offers a promising approach for decarbonizing energy-intensive industries. The CL-RWGS promotes the formation of surface oxygen vacancies in the material, which are subsequently replenished by extracting oxygen from CO2, resulting in syngas production. However, there remains a significant gap in the development of materials that not only exhibit redox activity but also enable in-situ carbonation, offering dual functionality for enhanced CO2 utilization. This study introduces a novel calcium- and manganese-doped LaNiO3 perovskite, designed for integrated CO2 sorption and in-situ utilization during CL–RWGS process. Comprehensive characterization confirmed the material’s crystalline structure, porosity, and successful incorporation of Ca and Mn dopants. Thermogravimetric analysis (TGA) across 700 – 900 °C revealed a peak oxygen storage capacity of 1.97 mmol O2/g and demonstrated excellent redox stability, with less than 1 % performance loss over 17 cycles. RWGS experiments conducted in a packed bed reactor demonstrated up to 57 % CO2 to CO conversion at 900 °C, approaching the thermodynamic equilibrium value of 60 % under the same operating conditions. Moreover, an H2/CO molar ratio of ∼2.0, suitable for Fischer-Tropsch synthesis, was achieved at 600 °C and 1.0 bar with a feed H2/CO2 molar ratio of 1.0, attributed to CO2 chemisorption via a carbonation-driven mechanism facilitated by the presence of CaO phase. These results suggest that the calcium- and manganese-doped LaNiO3 perovskite is a highly promising multi-functional material for chemical looping-based CO2 utilization technologies.
| Original language | English |
|---|---|
| Article number | 119640 |
| Journal | Journal of Environmental Chemical Engineering |
| Volume | 13 |
| Issue number | 6 |
| Early online date | 5 Oct 2025 |
| DOIs | |
| Publication status | Published - 31 Dec 2025 |
Data Availability Statement
Data will be made available on request.Acknowledgements
Moreover, the authors would also like to acknowledge Dr. Vincenzo Spallina for providing access to the laboratory at the University of Manchester in the Sustainable PRocess INtensification Group (SPRING).Funding
The authors would like to thank the School of Chemistry and Chemical Engineering, University of Southampton for providing necessary research funding for this study.
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