An investigation of the source of calcium carbonate from the carbonated Portland cement: Based on the transformation of hydrates

Abstract

In this work, two PC pastes were used to carry out accelerated carbonation experiments, and phase assemblages of paste samples collected at different sampling depths were analyzed. The source of CaCO3 originating from the carbonation reaction of hydrates in cement was quantitatively determined by a novel method based on the transformation of hydrates. Experimental results indicated that the phase assemblages in the carbonated zone of two PC pastes showed minor differences. C(A)SH, ettringite, AFm-CO3, and unhydrated cement particles in the complete carbonation zone of two cement pastes were carbonated and transformed into other phases. For the surface of two PC pastes (0–3 mm), calculations showed that the CaCO3 originating from the carbonation of calcium hydroxide and C(A)SH accounted for 75.3% and 72.6% of the total CaCO3, respectively. A concentration of 20% CO2 was not beneficial for the diffusion of CO2 and the subsequent precipitation of CaCO3 at the later period of carbonation.