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Undeclared uranium hitches a ride on cobalt exports from Congo, study says
Philippe (left) and Manzuk quantified the amount of uranium that has been exported from the DRC in cobalt shipments or left behind in the environment. (Photo: Joel Hallberg/UW–Madison)
Researchers at the University of Wisconsin–Madison and Princeton University have published a study in Nature Communications that calls attention to a blind spot in nuclear nonproliferation: The Democratic Republic of the Congo (DRC) has exported thousands of metric tons of uranium, and there is no accounting for where it has gone.
In partnership with Lighthouse Reports and the Financial Times, UW–Madison nuclear engineering professor and nuclear security expert Sébastien Philippe and Ryan Manzuk, a geologist and research fellow in Philippe’s group and at Princeton, conducted the study using countrywide mineralization and geochemical data.
G. F. Kessinger, M. C. Thompson
Nuclear Technology | Volume 169 | Number 3 | March 2010 | Pages 263-270
Technical Paper | Reprocessing | doi.org/10.13182/NT10-A9378
Articles are hosted by Taylor and Francis Online.
The primary goal of this investigation was to evaluate the effectiveness of the chop-leach process, with nitric acid solvent, to produce a nominally 300 g/l [U] and 1 M [H+] product solution. The results of this study show that this processing technique is appropriate for applications in which a low free acid and moderately high U content are desired. The 7.75 l of product solution, which was >450 g/l in U, was successfully diluted to produce [approximately]13 l of solvent extraction feed that was 302 g/l in U with a [H+] in the range 0.8 to 1.2 M.A secondary goal was to test the effectiveness of this treatment for the removal of actinides from Zircaloy cladding to produce a low-level radioactive waste (LLW) cladding product. Analysis of the cladding shows that actinides are present in the cladding at a concentration of [approximately]5000 Ci/g, which is about 50 times greater than the acceptable transuranium element limit in LLW.It appears that the concentration of nitric acid used for this dissolution study (initial concentration 4 M, with 10 M added as the dissolution proceeded) was inadequate to completely digest the UO2 present in the spent fuel. The mass of insoluble material collected from the initial treatments with nitric acid, 340 g, was much higher than expected, and analysis of this insoluble residue showed that it contained at least 200 g U.