Crystal Chemistry of Carnotite in Abandoned Mine Wastes.

Minerals (Basel)

Department of Civil, Construction & Engineering, MSC01 1070, Center for Water and the Environment, University of New Mexico, Albuquerque, NM 87131, USA.

Published: October 2020

The crystal chemistry of carnotite (prototype formula: K(UO)(VO)·3HO) occurring in mine wastes collected from Northeastern Arizona was investigated by integrating spectroscopy, electron microscopy, and x-ray diffraction analyses. Raman spectroscopy confirms that the uranyl vanadate phase present in the mine waste is carnotite, rather than the rarer polymorph vandermeerscheite. X-ray diffraction patterns of the carnotite occurring in these mine wastes are in agreement with those reported in the literature for a synthetic analog. Carbon detected in this carnotite was identified as organic carbon inclusions using transmission electron microscopy (TEM) and electron energy loss spectroscopy (EELS) analyses. After excluding C and correcting for K-drift from the electron microprobe analyses, the composition of the carnotite was determined as 8.64% KO, 0.26% CaO, 61.43% UO, 20.26% VO, 0.38% FeO, and 8.23% HO. The empirical formula, (K Ca Al(OH) Fe(OH) )((U)O)((V)O)·4HO of the studied carnotite, with an atomic ratio 1.9:2:2 for K:U:V, is similar to the that of carnotite (K(UO)(VO)·3HO) reported in the literature. Lattice spacing data determined using selected area electron diffraction (SAED)-TEM suggests: (1) complete amorphization of the carnotite within 120 s of exposure to the electron beam and (2) good agreement of the measured -spacings for carnotite in the literature. Small Differences between the measured and literature -spacing values are likely due to the varying degree of hydration between natural and synthetic materials. Such information about the crystal chemistry of carnotite in mine wastes is important for an improved understanding of the occurrence and reactivity of U, V, and other elements in the environment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793562PMC
http://dx.doi.org/10.3390/min10100883DOI Listing

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