Abstract

AbstractThe addition of CaCO3 powder in calcium aluminate cement (CAC) is reported to accelerate the hydration of CAC and generate mono‐carbonate C4AC̅H11, which is conducive to shortening the curing time of CAC‐bonded castables at ambient temperatures. Although the hydration of CAC is relatively fast, there is still residual un‐hydrated CAC in castables after curing. The residual CAC would continue to hydrate to produce C3AH6 and AH3 during the subsequent drying procedures in the absence of CaCO3. But it is worth pondering which type of hydrate would be generated in the presence of CaCO3 during the drying at around 110°C. In this study, the effect of micro‐sized CaCO3 addition on the hydrate formation of CAC‐bonded castables during drying at 110°C was investigated. The results indicate that the C4AC̅H11 formed at the curing temperature of 30°C is not decomposed or converted during drying. The CaCO3 remained after curing does not participate in the hydration of residual CAC during drying at 110°C, and thus the residual CAC continues to hydrate to generate C3AH6 rather than C4AC̅H11.

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