Abstract
Carbonation has been considered as an alternative to prevent CO2 leakage. In this study, calcium-doped mesoporous silica (CDMS) was introduced into Portland cement as a promoter of carbonation. An admixture of CDMS and American Petroleum Institute (API) Class G Portland cement exposed to CO2-saturated water was analyzed under geologic sequestration conditions (40°C and 80MPa) to assess the carbonation properties and self-healing effect of CDMS for CO2 storage. The capacity of CDMS to synthesize CaCO3 from CO2via carbonation was identified in an in vitro crystallization test. Analysis of the cut surface of a cement core showed the rapid synthesis of CaCO3 including calcite and aragonite. Rietveld analysis was employed for quantitative phase analysis. The quantitative analysis of the cement carbonation showed that tricalcium silicate (C3S) and dicalcium silicate (C2S) play important roles in cement carbonation. Several crystal phases of CaCO3 were identified in this study including calcite, aragonite and amorphous CaCO3. X-ray diffractometry (XRD), a field emission-scanning electron microscope (FE-SEM) equipped with an energy dispersive X-ray spectrometer (EDS), 29Si MAS-NMR (magic angle spinning–nuclear magnetic resonance) spectrometry, thermogravimetry-differential thermal analysis (TG-DTA) and FT-IR (Fourier transform infrared spectroscopy) were applied to characterize the admixture.
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