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American Mineralogist; April 2005; v. 90; no. 4; p. 672-678; DOI: 10.2138/am.2005.1742
© 2005 Mineralogical Society of America
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Direct formation of the {gamma}-CaSO4 phase in dehydration process of gypsum: In situ FTIR study

P.S.R. Prasad1,*, V. Krishna Chaitanya2, K. Shiva Prasad1 and D. Narayana Rao2

1 National Geophysical Research Institute, Hyderabad 500 007, India
2 School of Physics, University of Hyderabad, Hyderabad 500 046, India

Correspondence: * E-mail: psrprasad{at}ngri.res.in

The dehydration mechanism of natural single crystals of gypsum was investigated in the temperature range 300–430 K by in situ infrared (FTIR) spectroscopy. The thermal evolution of the second-order modes of H2O and SO4 groups in gypsum, in the wavenumber range 4850–5450 cm–1 and 2050–2300 cm–1 respectively, were used to probe the dehydration and rehydration sequence. A total disappearance of the combination modes of H2O and the replacement of four SO4–2 bands (2245, 2200, 2133, and 2117 cm–1) observed at room temperature by three bands (2236, 2163, and 2131 cm–1) observed at 390 K indicates the direct formation of {gamma}-CaSO4 upon heating. Upon cooling water re-enters into the {gamma}-CaSO4 structure at around 363 K to form bassanite. This observation, that the dehydration of gypsum directly yields {gamma}-CaSO4 (anhydrite) without the intermediate formation of hemi-hydrate (bassanite), is further corroborated by the dehydration behavior of bassanite. The second-order SO4 modes of bassanite observed around 2218, 2136, and 2096 cm–1 were replaced with the bands of {gamma}-CaSO4 at about 378 K upon heating.




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