Research output: Contribution to journal › Review article › peer-review
Crystal chemistry and structural complexity of the uranyl carbonate minerals and synthetic compounds. / Gurzhiy, Vladislav V.; Kalashnikova, Sophia A.; Kuporev, Ivan V.; Plášil, Jakub.
In: Crystals, Vol. 11, No. 6, 704, 19.06.2021.Research output: Contribution to journal › Review article › peer-review
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TY - JOUR
T1 - Crystal chemistry and structural complexity of the uranyl carbonate minerals and synthetic compounds
AU - Gurzhiy, Vladislav V.
AU - Kalashnikova, Sophia A.
AU - Kuporev, Ivan V.
AU - Plášil, Jakub
N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/6/19
Y1 - 2021/6/19
N2 - Uranyl carbonates are one of the largest groups of secondary uranium(VI)-bearing natural phases being represented by 40 minerals approved by the International Mineralogical Association, overtaken only by uranyl phosphates and uranyl sulfates. Uranyl carbonate phases form during the direct alteration of primary U ores on contact with groundwaters enriched by CO2, thus playing an important role in the release of U to the environment. The presence of uranyl carbonate phases has also been detected on the surface of “lavas” that were formed during the Chernobyl accident. It is of interest that with all the importance and prevalence of these phases, about a quarter of approved minerals still have undetermined crystal structures, and the number of synthetic phases for which the structures were determined is significantly inferior to structurally characterized natural uranyl carbonates. In this work, we review the crystal chemistry of natural and synthetic uranyl carbonate phases. The majority of synthetic analogs of minerals were obtained from aqueous solutions at room temperature, which directly points to the absence of specific environmental conditions (increased P or T) for the formation of natural uranyl carbonates. Uranyl carbonates do not have excellent topological diversity and are mainly composed of finite clusters with rigid structures. Thus the structural architecture of uranyl carbonates is largely governed by the interstitial cations and the hydration state of the compounds. The information content is usually higher for minerals than for synthetic compounds of similar or close chemical composition, which likely points to the higher stability and preferred architectures of natural compounds.
AB - Uranyl carbonates are one of the largest groups of secondary uranium(VI)-bearing natural phases being represented by 40 minerals approved by the International Mineralogical Association, overtaken only by uranyl phosphates and uranyl sulfates. Uranyl carbonate phases form during the direct alteration of primary U ores on contact with groundwaters enriched by CO2, thus playing an important role in the release of U to the environment. The presence of uranyl carbonate phases has also been detected on the surface of “lavas” that were formed during the Chernobyl accident. It is of interest that with all the importance and prevalence of these phases, about a quarter of approved minerals still have undetermined crystal structures, and the number of synthetic phases for which the structures were determined is significantly inferior to structurally characterized natural uranyl carbonates. In this work, we review the crystal chemistry of natural and synthetic uranyl carbonate phases. The majority of synthetic analogs of minerals were obtained from aqueous solutions at room temperature, which directly points to the absence of specific environmental conditions (increased P or T) for the formation of natural uranyl carbonates. Uranyl carbonates do not have excellent topological diversity and are mainly composed of finite clusters with rigid structures. Thus the structural architecture of uranyl carbonates is largely governed by the interstitial cations and the hydration state of the compounds. The information content is usually higher for minerals than for synthetic compounds of similar or close chemical composition, which likely points to the higher stability and preferred architectures of natural compounds.
KW - Carbonate
KW - Crystal structure
KW - Mineral
KW - Structural complexity
KW - Topology
KW - Uranyl
KW - ANDERSONITE
KW - uranyl
KW - topology
KW - X-RAY-DIFFRACTION
KW - RAMAN
KW - URANIUM MINERALS
KW - U6+ MINERALS
KW - SAN-JUAN COUNTY
KW - MARKEY MINE
KW - crystal structure
KW - structural complexity
KW - SPECTROSCOPIC CHARACTERIZATION
KW - LIEBIGITE
KW - mineral
KW - carbonate
KW - RUTHERFORDINE
UR - http://www.scopus.com/inward/record.url?scp=85109110386&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/197dfaee-cbbf-3765-a122-67d96dd6af8e/
U2 - 10.3390/cryst11060704
DO - 10.3390/cryst11060704
M3 - Review article
AN - SCOPUS:85109110386
VL - 11
JO - Crystals
JF - Crystals
SN - 2073-4352
IS - 6
M1 - 704
ER -
ID: 78837973