Abstract
The nucleation of a mineral crystal and its growth in groundwater carrying fractures 300 m above the Palmottu uranium deposit provide an impressive example of geochemical selectivity of uranium. Fracture-filling material was collected from a 3 mm thick fracture at depth 74.8 - 75 m (drillcore R348). SEM and EDS analyses on a thin section of the original fracture-filling show that the fracture filling is heterogeneous, composing mineral crystal particles and very porous clay-rich aggregates. The results of INAA on millimetre-sized single mineral crystals and aggregates selected from grinded fracture-filling show that porous aggregates (composed of clays and micrometer sized mineral particles) contain up to 1000 ppm U, which is higher than the average of the whole fracture-filling (400 ppm) and host rock related millimetre sized mineral particles (18 - 100 ppm). 233U/238U isotope exchange proves that a large fraction of the uranium in the fracture-filling is not easily exchanged with uranium in the solution. The amount of 238U released in the isotope exchange experiment is too high to be explained by reversible U(VI) sorption. Oxidation state analyses show that 30% of the uranium exists as U(IV). Laboratory batch experiment at anoxic conditions proved that pyrite can immobilise U(VI).
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