Structure–Superstructure Inter-Relations in Ca2SiO4 Belite Phase

Abstract

Belite, the second most abundant mineralogical phase in Portland cement, presents five polymorphs which are formed at different temperatures. The increased interest in belite cement-based products is due to the lower environmental impact associated with the lower energy consumption. The importance of belite polymorphs formed at higher temperatures for cement industry applications is high, because they present better hydraulic properties. Thus, any study that helps to explore the structure relations of all belite polymorphs is of interest for both scientific and practical points of view. In the present work, a systematic structure–superstructure relation study is presented for all polymorphs, and it is based on the work of O’Keefe and Hyde (1985). In this pioneering work, generally, the structures of oxides are considered as having common characteristics with prototype structures of alloys. The basic result of the present work is the fact that all the polymorphs adopt a common architecture which is based on capped trigonal prisms of Ca cations, which host the Si one, and the oxygen anions occupy interstitial sites, i.e., an architecture in conformity with the model which considers the oxide structures as stuffed alloys. This result supports the displacive character of the transformation structural mechanism that links the five polymorphs based on the cation sites in their structures. However, based on the sites of oxygen anions, it could be considered as of diffusion character. The study of belite polymorphs is also of interest to products obtained by doping dicalcium silicate compounds, which present interesting luminescent properties.