Metal–organic frameworks (MOFs) show great potential for post-combustion carbon capture, yet their practical application is often constrained by challenges such as powder handling difficulties, limited structural stability during shaping processes, and performance degradation under high-humidity conditions. In this study, Mg-gallate was structured into millimeter-sized Mg-gallate/CA composite beads via the ionotropic gelation method, and then a hydrophobic layer of vinyltrimethoxysilane (VTMS) was constructed on the bead surface by chemical vapor deposition. The synthesized Mg-gallate/CA and V-Mg-gallate/CA are characterized by XRD, FT-IR, and other techniques, and their CO2 adsorption behavior, adsorption–desorption kinetics, breakthrough performance, and cyclic stability are systematically evaluated. At 298 K and 0.1 bar, the CO2 adsorption capacity of Mg-gallate/CA reached 94.2% of that of Mg-gallate powder. The microporous–microporous hierarchical structure constructed by the ionotropic gelation method improved the CO2 capture efficiency of the composite beads by 16.7% at 0.1 bar. V-Mg-gallate/CA maintained a high dynamic CO2 adsorption capacity of 2.87 mmol/g for a 10 vol.% CO2/90 vol.% N2 gas mixture at 298 K under 80% RH, corresponding to 2.04 times the capacity of Mg-gallate/CA, and retained 98.8% of its initial adsorption capacity at 0.1 bar after 10 cycles. Combining ionotropic gelation shaping with surface hydrophobic modification represents an effective strategy for developing MOF-based adsorbents suitable for post-combustion CO2 capture.
Wang et al. (Thu,) studied this question.