Accelerated Carbonation as a Potential Alternative for Autoclaved Fiber Cement Material—A Comparison in Macro and Micro Scale

This study investigates accelerated carbonation as a low-energy alternative to autoclave curing in the production of fiber cement composites reinforced with lignocellulosic fibers. The effects of both curing routes on physical–mechanical performance, durability, and microstructural evolution were systematically evaluated before and after 25 wetting–drying cycles. Carbonation-cured composites achieved mechanical performance comparable to autoclaved materials, while exhibiting higher bulk density (≈1.37–1.38 g/cm3) and a reduction of approximately 15% in total void volume. Water absorption values were up to 17% lower than those of autoclaved counterparts. After accelerated aging, both systems showed stable mechanical properties, with increases in modulus of elasticity of approximately 21% (autoclaved) and 26% (carbonated), indicating ongoing hydration and densification processes. Thermogravimetric analysis revealed carbonation degrees of approximately 16–17%, corresponding to CO2 uptake values of up to 35.8 kg/m3 of fiber cement. X-ray diffraction confirmed the consumption of portlandite and the formation of calcium carbonate phases, contributing to pore refinement and matrix densification. Microstructural observations indicated improved fiber–matrix interaction in carbonated composites due to the precipitation of carbonation products at the interface, whereas autoclaved materials exhibited signs of fiber degradation associated with hydrothermal curing. These effects were reflected in higher deformation capacity and specific energy retention in carbonated systems. Overall, accelerated carbonation represents a promising alternative to autoclave curing, delivering comparable mechanical performance while enhancing fiber durability, refining pore structure, and enabling CO2 sequestration within the cementitious matrix.