Natural carbonation process in cement paste particles in different relative humidities

Abstract

Finely ground hardened cement pastes (hcp) under 75 μm were carbonated at varying relative humidities (23–95 % RH) to determine the carbonation rate that minimized CO2 diffusion in the bulk paste. The amounts of portlandite (CH) and calcium carbonate (CC) polymorphs were quantified, and the decalcification and decomposition of C-A-S-H were analyzed using TGA, XRD, mass balance calculation, FTIR, and 29Si MAS NMR spectroscopy. A higher RH accelerated the reaction rate, and CH dissolution stopped midway at 58 % RH or below because of the loss of connectivity with the pore solution in the CC shell around CH. The precipitated CC phase included calcite at high RH, whereas all three polymorphs formed at 58 % or lower RH; amorphous CC were detected at low RH. The decalcification and decomposition of C-A-S-H were observed at 45 % or higher RH; it was rarely carbonated at 33 % or lower RH.