The setting behaviour of alpha- and beta-CaSO4 center dot 0,5 H2O as a function of crystal structure and morphology

Abstract

Calcium sulphate subhydrates (CaSO4 (.) x H2O 0 < x less than or equal to 0.8) have a honeycomb-shaped channel structure. The symmetry is either trigonal or a slight deviation thereof Due to insufficient diffraction data and the high pseudosymmetry of the structure, it is not possible at this point to determine with certainty the specific arrangement of the water molecules in the channels. When the Fourier transformation method is used to calculate the growth form of the hemihydrate (x = 0.5), the calculated crystal form corresponds to the observed form only when the trigonal structural symmetry is largely retained. During dehydration of gypsum or, conversely, during the setting process of hemihydrate, heteroepitaxial growths of hemihydrate are observed on gypsum, or gypsum is grown heteroepitaxially on hemihydrate. The (100) faces of the hemihydrate and (010) of gypsum for the most part run parallel. Using diffraction and spectroscopic methods, it can be shown that a structural difference exists between alpha- and beta-hemihydrates, and that this difference probably accounts for the different setting bebaviours. It is in this context that the presence of oxonium ions, particularly in beta-hemihydrate, found in NMR experiments is of interest. Textural studies indicated that the arrangement of gypsum crystals found in hardened gypsum is determined by the hemihydrate.