On the crystallisation pressure of gypsum

We estimate the crystallisation pressure of gypsum quantitatively, with reference to the geological context of the Gypsum Keuper formation. The formation contains sulphatic claystones which have the property of swelling in the presence of water and have caused substantial structural damage to the linings of several tunnels in Switzerland and Germany. The swelling of these rocks is attributed to the transformation of anhydrite into gypsum, which occurs via the dissolution of anhydrite in pore water and the precipitation of gypsum from the solution. This simultaneous dissolution–precipitation process happens because the solubility of gypsum is lower than that of anhydrite under the conditions prevailing after tunnelling, and it does not cease until all of the anhydrite has been transformed. The elementary mechanism behind the development of the macroscopically observed swelling pressure is the growth of gypsum crystals inside the rock matrix: If a crystal is in contact with a supersaturated solution, but its growth is prevented by the surrounding matrix, it then exerts a so-called crystallisation pressure upon the pore walls. In the present paper, the crystallisation pressure is calculated by means of a thermodynamic model that takes coherent account of all relevant parameters, including the chemical composition of the pore water and pore size. Variations in these parameters lead to a very wide range of crystallisation pressures (from zero to several tens of megapascals). By using the results of mercury intrusion porosimetry and chemical analyses of samples from three Swiss tunnels, however, we show that the range of predicted values can be reduced significantly with the help of standard, project-specific investigations.ISSN:1866-6280ISSN:1866-629