In this study, carbon dioxide (CO 2 ) was sequestered in the curing of wood-sodium silicate (SS) composites. The effect of carbonation curing pressure, reaction time, wood fiber particle size, and post curing temperature on the thermal and mechanical properties of wood-SS composites was investigated. A mixture of 50 wt % wood (40 and 200-mesh) and SS was used to fabricate composites that were considered for carbonation curing. Dynamic rheological behavior of the blends during isothermal curing showed a higher complex viscosity for CO 2 -treated samples. X-ray microcomputed tomography (micro-CT) scans showed an increased CO 2 penetration depth with carbonation time and pressure. The %CO 2 uptake for wood-SS samples increased with the CO 2 exposure time and pressure. Curing kinetics of neat SS and wood-SS composites of different wood contents (50−70 wt %), examined using modulated dynamic scanning calorimetry (MDSC), showed activation energies ranged from 85 to 125 kJ/mol. The flexural properties of the 200-mesh wood-SS composites were higher with flexural modulus between 0.8 to 11.2 GPa and flexural strength between 3.5 to 59.2 MPa. Statistical response surface methodology showed that the CO 2 pressure and exposure time had significant effects on the mechanical properties of carbonated cured wood-SS composites.