Abstract

The effects of various initial carbonation curing environments on the phase evolution and resulting mechanical characteristics of tricalcium silicate paste were studied. For the analyses of the reaction products and microstructure, synchrotron X-ray diffraction, thermogravimetry, Fourier transform-infrared spectroscopy, scanning electron microscopy with energy dispersive X-ray spectroscopy and high-resolution X-ray computed tomography were utilized. C3S cured under carbonation environment pressurized by 0.1 MPa showed excellent mechanical properties owing to the highest degree of reaction and homogeneous generation of CaCO3 with low-Ca/Si calcium silicate hydrates, resulting in a dense matrix with refined pore structure. C3S paste treated under other carbonation conditions underwent deteriorative microstructural phase transitions, including void evolution by decalcification of C–S–H and an inhomogeneous composition of crystalline phases, resulting in inferior properties.

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