M. Fortunato, Elisabetta Maria Cepollaro, L. Lisi, Stefano Cimino
Integrated CO 2 capture and methanation (ICCM) is attracting growing interest as a circular net-zero technology to convert dilute waste CO 2 into synthetic natural gas using green hydrogen. However, its effective deployment requires dual-function materials (DFMs) that balance high CO 2 adsorption capacity with fast, selective methanation kinetics under realistic cyclic conditions. This work systematically evaluates Ru-based DFMs supported on hydrotalcite-derived (Mg Al) oxides promoted by K or Na. The effect of alkali promotion on CO 2 uptake, hydrogenation kinetics and cyclic ICCM performance is investigated under both ideal (5% CO 2 /N 2 ) and realistic feeds containing H 2 O and O 2 during the capture stage. DFM performance is correlated with surface chemistry through combined transient ICCM experiments in the fixed-bed reactor and operando DRIFTS studies. The Ru/Na-Mg-Al is identified as the most balanced DFM, capturing as much as 550 μmol CO 2 g −1 DFM in the presence of water vapour and converting it to CH 4 with high selectivity and remarkable stability across cycles at 340–400 °C. Particular emphasis is placed on methane productivity under cyclic operation, as a key performance indicator for material development and process intensification under realistic feed conditions. • Novel DFMs for ICCM with low Ru load on high-capacity hydrotalcite-derived supports • Cyclic ICCM performances extensively assessed under realistic H 2 O and O 2 containing feeds • Na-promoted DFM largely outperforms K- balancing CO 2 uptake and methanation activity • Water enhances CO 2 capture capacity at the expense of slower methanation kinetics. • Mechanistic insights from transient operando DRIFTS during ICCM cycles