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Solution-driven processing of calcium sulfate : the mechanism of the reversible transformation of gypsum to bassanite in brines

MPG-Autoren
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Scoppola,  Ernesto       
Wolfgang Wagermaier, Biomaterialien, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

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Zitation

Stawski, T., Karafiludis, S., Pimentel, C., Montes-Hernandez, G., Kochovski, Z., Bienert, R., et al. (2024). Solution-driven processing of calcium sulfate: the mechanism of the reversible transformation of gypsum to bassanite in brines. Journal of Cleaner Production, 440: 141012. doi:10.1016/j.jclepro.2024.141012.


Zitierlink: https://hdl.handle.net/21.11116/0000-000D-B6A3-D
Zusammenfassung
Here, we show that calcium sulfate dihydrate (gypsum) can be directly, rapidly and reversibly converted to calcium sulfate hemihydrate (bassanite) in high salinity solutions (brines). The optimum conditions for the efficient production of bassanite in a short time (< 5 min) involve the use of brines with [NaCl] > 4 M and maintaining a temperature, T > 80 °C. When the solution containing bassanite crystals is cooled down to around room temperature, eventually gypsum is formed. When the temperature is raised again to T > 80 °C, bassanite is rapidly re-precipitated. This contrasts with the typical behaviour of the bassanite phase in low salt environments. Traditionally, hemihydrate is obtained from gypsum through a solid state thermal treatment at 150 °C < T < 200 °C, to remove some of the structural water. This is because, bassanite is considered to be metastable with respect to gypsum and anhydrite in aqueous solutions, and therefore gypsum-to-bassanite conversion should not occur in water. Interestingly, the high-salinity transformation of gypsum-to-bassanite has been reported by many authors and used in practice for several decades, although its very occurrence actually contradicts numerical thermodynamic predictions regarding solubility of calcium sulfate phases. By following the evolution of crystalline phases with in situ and time-resolved X-ray diffraction/scattering and Raman spectroscopy, we demonstrated that the phase stability in brines at elevated temperatures is inaccurately represented in the thermodynamic databases. Most notably for [NaCl] > 4 M, and T > 80 °C gypsum becomes readily more soluble than bassanite, which induces the direct precipitation of the latter from gypsum. The fact that these transformations are controlled by the solution provides extensive opportunities for precise manipulation of crystal formation. Our experiments confirmed that bassanite remained the sole crystalline structure for many hours before reverting into gypsum. This property is extremely advantageous for practical processing and efficient crystal extraction in industrial scenarios.