Microbial reduction
of soluble hexavalent uranium (U(VI)) to sparingly
soluble tetravalent uranium (U(IV)) has been explored as an
in situ
strategy to immobilize U. Organic ligands might
pose a potential hindrance to the success of such remediation efforts.
In the current study, a set of structurally diverse organic ligands
were shown to enhance the dissolution of crystalline uraninite (UO
2
) for a wide range of ligand concentrations under anoxic conditions
at pH 7.0. Comparisons were made to ligand-induced U mobilization
from noncrystalline U(IV). For both U phases, aqueous U concentrations
remained low in the absence of organic ligands (<25 nM for UO
2
; 300 nM for noncrystalline U(IV)). The tested organic ligands
(2,6-pyridinedicarboxylic acid (DPA), desferrioxamine B (DFOB),
N
,
N
′-di(2-hydroxybenzyl)ethylene-diamine-
N
,
N
′-diacetic acid (HBED), and citrate)
enhanced U mobilization to varying extents. Over 45 days, the ligands
mobilized only up to 0.3% of the 370 μM UO
2
, while
a much larger extent of the 300 μM of biomass-bound noncrystalline
U(IV) was mobilized (up to 57%) within only 2 days (>500 times
more
U mobilization). This work shows the potential of numerous organic
ligands present in the environment to mobilize both recalcitrant and
labile U forms under anoxic conditions to hazardous levels and, in
doing so, undermine the stability of immobilized U(IV) sources.