Abstract
Additions of carbon dioxide to hydrating concrete have been observed to result in performance benefits. In this study, oil-well cement (selected for its very low initial carbonate content) was hydrated in the presence and absence of pure CO2 gas. The evolution of the products and reactants was assessed through isothermal calorimetry, Quantitative X-ray Diffraction (QXRD), Loss on Ignition, and Total Inorganic Carbon. A one minute exposure to carbon dioxide gas during mixing improved the heat of hydration though 24 h by 8%. The amount of C-S-H formed increased by 20%, and the estimated degree of hydration increased by 23%. The carbon dioxide promoted the formation of calcium carbonate that was observed in the sample immediately after treatment with carbon dioxide. The carbonate was initially amorphous calcium carbonate not detectable with QXRD, but it changed over 24 h to crystalline calcite (CaCO3) detectable by QXRD.
Acknowledgements
The authors would like to thank Diane Praught at CarbonCure Technologies for completing the calorimetry, and Anna Harrison at UBC for assistance in XRD data collection and interpretation. The industrial work was completed with the support of Argos in Cumming, Georgia. The useful comments and suggestions of the anonymous journal reviewers are also appreciated.