Abstract:
CO
2 is the predominant greenhouse gas in the atmosphere, and the development of efficient CO
2 capture and utilization technologies is crucial for achieving carbon peaking and carbon neutrality. Calcium-based adsorbents have attracted extensive attention because of their excellent CO
2 capture capability, while nickel-based catalysts are widely used in developing Ca-Ni bifunctional materials due to their outstanding catalytic performance. Doping with Ce-containing promoters can further improve the efficiency and stability of these materials. However, commonly used sorbents still suffer from low efficiency, high cost, and poor sintering resistance. In this work, a Ca-Ni-Ce composite system was investigated. A series of CaO-Ni-CeO
2 composite samples with different CeO
2 loadings were synthesized via a citrate complexation method, and their physicochemical properties were characterized by XRD, SEM, etc. Thermogravimetric analysis was employed to evaluate the CO
2 uptake of the samples under cyclical conditions, and the effects of CO
2 concentration and carbonation temperature on their capture performance were systematically investigated. The results indicate that doping with an appropriate amount of CeO
2 can effectively enhance the CO
2 capture performance of the composites. The optimal CeO
2 content maintains sufficient active sites while effectively inhibiting sintering, thereby significantly improving the stability of the sorbent over multiple cycles. Among the four groups of samples, the Ni-Ca
10Ce sample exhibited the best sintering resistance and CO
2 capture efficiency, with an average CO
2 uptake of 0.46 g·g
−1 sor and an average carbonation conversion of 94.35% over 20 thermogravimetric cycles. Increasing CO
2 concentration promotes the carbonation reaction. Specifically, the adsorption efficiency improved significantly as the concentration rose up to 20 vol.%, beyond which further concentration increases yielded no substantial improvement due to the near-complete saturation of active sites. Additionally, a moderate increase in reaction temperature promotes the chemisorption of CO
2 molecules on the CaO surface, enhancing the surface reaction rate by reducing the activation energy. Therefore, 650 °C was identified as the optimal temperature to balance material activity and adsorption efficiency. Considering long-term stability and economic viability, the temperature should not exceed 700 °C to prevent material sintering and attrition. This study provides a technical reference for the preparation and optimization of new CO
2 capture materials and offers an effective strategy for industrial carbon neutrality.