The Hydration of β- and α′H‑Dicalcium Silicates: An X‑ray Spectromicroscopic Study
Published Web Locationhttps://doi.org/10.1021/acssuschemeng.8b05060
Dicalcium silicate (C 2 S) is an important clinker mineral in Portland and belite-calcium sulfoaluminate cement. However, there is still a lack of information on the local degree of silicate polymerization and calcium coordination in C 2 S hydration products. This study aimed to fill this gap by characterizing the hydration of two C 2 S polymorphs, the β- and α′ H - types, using scanning transmission X-ray microscopy coupled with ptychographic imaging. The results showed that the coordination of the Ca species in β- and α′ H -C 2 S had a distorted, cubic-like symmetry, whereas the Ca coordination of calcium silicate hydrate (C-S-H), the main hydration product, was structurally similar to that of tobermorite. The outer hydration product (Op) of both polymorphs exhibited an increasing degree of silicate polymerization over time. The inner hydration product (Ip) of β-C 2 S polymerized slower than Op; however, the degree of silicate polymerization of both Ip and Op in the α′ H -C 2 S hydration system was comparable. The polymerization degree of Op was relatively heterogeneous, whereas, in α′ H -C 2 S, the polymerization degree was more homogeneous. Ptychographic imaging shows that the Op of α′ H -C 2 S exhibits coarser fibrils than the Op of β-C 2 S, and a clear Op-Ip interface of hydrated β-C 2 S is observed.