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Published online 3 September 2009
Mineralogical Magazine; June 2009; v. 73; no. 3; p. 421-432; DOI: 10.1180/minmag.2009.073.3.421
© 2009 Mineralogical Society of Great Britain and Ireland
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Right arrow Articles by Jacques, S. D. M.
Right arrow Articles by Barnes, P.

Structural evolution during the dehydration of gypsum materials

S. D. M. Jacques1,*, A. González-Saborido1, O. Leynaud1, J. Bensted1, M. Tyrer2, R. I. W. Greaves2 and P. Barnes1

1 Department of Chemistry, University College London, 20 Gordon Street, London WC1H OAJ, UK and School of Crystallography, Birkbeck College, Malet Street, London WC1E 7HX, UK
2 Department of Materials, Imperial College, Prince Consort Road, South Kensington, London SW7 2BP, UK

* E-mail: s.jacques{at}mail.cryst.bbk.ac.uk

The dehydration of pure and waste gypsums has been examined using in situ synchrotron angle-dispersive X-ray diffraction. Pure gypsum was studied under a number of defined environments; various industrial waste gypsums were also studied under a common standard environment. It is found that the dehydration of gypsum to anhydrite proceeds via the hemihydrate and {gamma}-anhydrite phases and the interplay and behaviour of these phases has been determined by full structural `Rietveld' refinement. In the study of the pure gypsum system, the hemihydrate structure is shown to be preserved as water is lost. A `zero-water hemihydrate' is observed before refinement in the higher symmetry {gamma}-anhydrite cell is possible. The waste gypsum materials studied showed significant differences in the temperatures at which key transformation events occurred; these observations raise implications concerning the re-use of by-product gypsum materials. Finally, high temperature data are re-examined in the search for a variation of the anhydrite structure.

KEYWORDS: gypsum, dehydration







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