Temperature dependence, 0 to 40 °C, of the mineralogy of Portland cement paste in the presence of calcium carbonate

Thermodynamic calculations disclose that significant changes of the AFm and AFt phases and amount of Ca(OH)2 occur between 0 and 40 °C; the changes are affected by added calcite. Hydrogarnet, C3AH6, is destabilised at low carbonate contents and/or low temperatures < 8 °C and is unlikely to form in calcite-saturated Portland cement compositions cured at < 40 °C. The AFm phase actually consists of several structurally-related compositions which form incomplete solid solutions. The AFt phase is close to its ideal stoichiometry at 25 °C but at low temperatures, < 20 °C, extensive solid solutions occur with CO3-ettringite. A nomenclature scheme is proposed and AFm–AFt phase relations are presented in isothermal sections at 5, 25 and 40 °C. The AFt and AFm phase relations are depicted in terms of competition between OH, CO3 and SO4 for anion sites. Diagrams are presented showing how changing temperatures affect the volume of the solid phases with implications for space filling by the paste. Specimen calculations are related to regimes likely to occur in commercial cements and suggestions are made for testing thermal impacts on cement properties by defining four regimes. It is concluded that calculation provides a rapid and effective tool for exploring the response of cement systems to changing composition and temperature and to optimise cement performance.