Uranyl-oxide hydroxy-hydrate minerals; their structural complexity and evolution trends
Uranyl-oxide hydroxy-hydrate minerals; their structural complexity and evolution trends
European Journal of Mineralogy (September 2017) 30 (2): 237-251
- actinides
- Africa
- alteration
- Bohemia
- Central Africa
- Central Europe
- chemical composition
- Congo Democratic Republic
- coordination
- crystal structure
- Czech Republic
- Europe
- hydration
- hydroxides
- hydroxyl ion
- Jachymov Czech Republic
- metals
- oxidation
- oxides
- schoepite
- topology
- unit cell
- uraninite
- uranium
- water
- weathering
- vandendriesscheite
- vandenbrandeite
- Shinkolobwe Mine
- uranyl hydroxides
Uranyl-oxide hydroxy-hydrates (UOH) represent one of the most structurally and chemically complex families of naturally occurring U (super 6+) phases. To date, about 28 members are known as mineral species and a dozen others have been synthesized under laboratory conditions. The majority of these have been structurally characterized, showing an extraordinary complexity despite their relatively simple chemical composition; U, Pb, O and H are mostly the major constituents. Both the structural and chemical complexity of UOH minerals were determined with the program TOPOS, using complexity parameters that provide Shannon information content per atom and per unit cell and performula unit. The average content per unit cell, 1159 bits/cell shows that UOH minerals are extraordinary complex; this is in line with (1) the high coordination diversity, considering the transition of U (super 4+) to U (super 6+) during oxidation-hydration weathering of uraninite that leads to the formation of UOH phases; (2) incorporation of a large amount of H (super +) , in the form of H (sub 2) O and (OH) (super -) ; (3) incorporation of other elements during weathering, mostly K (super +) , Pb (super 2+) or Ca (super 2+) . The simplest UOH mineral is vandenbrandeite, triclinic, Cu (UO (sub 2) )(OH) (sub 4) , with 86 bits/cell. The most complex UOH mineral is vandendriesscheite, orthorhombic Pb (sub 1.5) [(UO (sub 2) ) (sub 10) O (sub 6) (OH) (sub 11) ](H (sub 2) O), with 4296 bits/cell, which owes its structural complexity to the presence of a large proportion of H (sub 2) O/OH and several symmetrically unique U sites in the structure. The general trend of the early-forming UOH minerals is a high molar proportion of U and H (sub 2) O/OH and lower proportion of metal cations. This leads in general to their complex character. The increase in complexity (both structural and chemical) is also related to the presence of metal cations in the structure with distinct stereochemistry, such as K (super +) , Fe (super 2+) ,Ca (super 2+) or Pb (super 2+) The overall trend is a steady increase of complexity (both structural and chemical) during continuous alteration. A discussion of occurrence trends and UOH complexity is given. One of the most complex structures among UOHs is schoepite, [(UO (sub 2) ) (sub 8) O (sub 2) (OH) (sub 12) ](H (sub 2) O) (sub 12) ( approximately 2593 bits/cell), which is reported from various localities worldwide. The relatively common occurrence of schoepite is probably because it is a very early alteration product, which is (1) complex and (2) easily distinguishable.