1The
University of Georgia, Savannah River Ecology Laboratory, Aiken, South Carolina
29802, USA 2Washington State University, Department of Chemistry, Pullman,
Washington 99164, USA 3Clemson University, Department of Environmental Engineering and
Science, Clemson, South Carolina 29634, USA
(Received September 20, 1999; accepted April 3, 2000)
Summary. The dehydration of uranyl
minerals can affectphase structure and stability. Synthetic autunite hydrates,Ca[(UO2)(PO4)]2.xH2O,
were studied by X-ray powderdiffractometry
(XRD) and thermogravimetric analysis (TGA)to
address ambiguous or contradictory reports in the literature.Structurally, XRD analysis supported the three well-definedphases commonly reported in the literature, i.e. autunite,
metaautunite I, and metaautunite II. In addition, a fourthphase with a basal plane spacing between that of autunite andmetaautunite I, designated metaautunite Ia, was identified as an
apparent metastable intermediate. TGA analysis confirmedthat water loss or accumulation is tolerated to different degreesamong the autunite hydrates. Loss of low temperature waterappears to initiate collapse of the interlayer spacing from 10to 9 Å to form metaautunite I and/or Ia, while the lowerhydrates accommodate minor water loss and accumulationwithout significant structural alteration. Our results supportprevious research indicating the reversibility of the autunite to
metaautunite I conversion. The complex dehydration
patternof autunite is
not observed in all the 1: 1 uranyl phosphates,such as chernikovite (H[(UO2)(PO4)].4H20).
SREL Reprint #2494
Sowder, A. G.,
S. B. Clark, and R. A. Fjeld. 2000. Dehydration of synthetic autunite hydrates.
Radiochim. Acta 88:533-538.