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American Mineralogist; August 2005; v. 90; no. 8-9; p. 1308-1314; DOI: 10.2138/am.2005.1568
© 2005 Mineralogical Society of America
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Dehydration processes in the meta-autunite group minerals meta-autunite, metasaléeite, and metatorbernite

Yohey Suzuki1, Tsutomu Sato2, Hiroshi Isobe3, Toshihiro Kogure4 and Takashi Murakami4,*

1 Frontier Research System for Extremophiles, Japan Marine Science and Technology Center, 2-15, Natsushima-cho, Yokosuka 237-006, Japan
2 Institute of Nature and Environmental Technology, Kanazawa University, Kanazawa, Ishikawa 920-1192, Japan
3 Department of Earth Science, Kumamoto University, Kumamoto, Kumamoto 860-8555, Japan
4 Department of Earth and Planetary Science, the University of Tokyo, Hongo, Tokyo 113-0033, Japan

Correspondence: * E-mail: murakami{at}eps.s.u-tokyo.ac.jp

We investigated dehydration processes in uranyl phosphate minerals of the meta-autunite group that consist of uranyl phosphate sheets and interlayer cations, and water molecules. Meta-autunite [Ca(UO2PO4)2·6H2O], metasaléeite [Mg(UO2PO4)2·8H2O], and metatorbernite [Cu(UO2PO4)2·8H2O] were selected for our study. The change in basal spacing between two adjacent uranyl phosphate sheets with temperature was examined by temperature-controlled X-ray diffraction (XRD) analysis from room temperature (RT) to 300 °C to determine structurally distinct, dehydrated phases. Thermogravimetric and differential thermal analyses (TG/DTA) were also performed under conditions similar to those used for the XRD analysis to clarify the hydration states of the dehydrated phases. Retention of the structure of the uranyl phosphate sheets under a high vacuum, equivalent to 300 °C, was confirmed by transmission electron microscopy. Meta-autunite, metasaléeite, and metatorbernite decreased their basal spacings by losing water molecules. Comparison of the TG/DTA and XRD results indicates that the changes in basal spacings of the dehydrated phases with temperature are as follows: 8.32 Å (6 H2O per unit formula) at RT, 7.31 (? H2O) and 6.68 Å (? H2O) at 75 °C, 6.34 Å (2 H2O) at 120 °C, and 5.81 Å (1 H2O) at 300 °C for meta-autunite; 8.29 (8 H2O) and 7.73 Å (? H2O) at RT, 6.62 Å (probably, 2 H2O) at 40 °C, 6.54 Å (2 H2O) at 160 °C, and 5.52 Å (1 H2O) at 300 °C for metasaléeite; and 8.61 Å (8 H2O) at RT, 8.07 Å (4 H2O) at 100 °C, 6.58 Å (2 H2O) at 200 °C, and 5.60 Å (1 H2O) at 300 °C for metatorbernite. The dehydration processes revealed by XRD and TG/DTA under similar experimental conditions are slightly different from those obtained by previous studies. Our results clearly demonstrate the presence of previously unknown dehydrated phases of the meta-autunite group minerals with basal spacings less than 6 Å that may have distinct thermodynamic properties.




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C. M. Smeaton, C. G. Weisener, P. C. Burns, B. J. Fryer, and D. A. Fowle
Bacterially enhanced dissolution of meta-autunite
American Mineralogist, November 1, 2008; 93(11-12): 1858 - 1864.
[Abstract] [Full Text] [PDF]




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