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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.
N. Prolingheuer, M. Herbst, B. Heuel-Fabianek, R. Moormann, R. Nabbi, B. Schlögl, J. Vanderborght
Nuclear Technology | Volume 168 | Number 3 | December 2009 | Pages 924-930
Dose/Dose Rate | Special Issue on the 11th International Conference on Radiation Shielding and the 15th Topical Meeting of the Radiation Protection and Shielding Division (PART 3) / Radiation Protection | doi.org/10.13182/NT09-A9328
Articles are hosted by Taylor and Francis Online.
At sites with powerful particle accelerators, the problem of groundwater activation by direct neutron radiation arises. Licensing of particle accelerators requires evidence that groundwater activation is within the legal limits and thus will not endanger workers, the public, or the environment.In this study we focus on the following radionuclides: 14C, 41Ca, 45Ca, 36Cl, 55Co, 57Co, 60Co, 3H, 54Mn, 24Na, 32P, 35S, 32Si, and 50V. The conventional approach for calculating activation of soil and groundwater is described and utilized for a fictive 5-MW proton accelerator at Jülich, Germany, with a beam loss of 1 Wm-1. An updated overview of partition coefficients for relevant radionuclides in sand, clay, loam, and organic soils is presented. Based on the two aforementioned methods, groundwater activation is estimated with a simplified homogeneous groundwater transport model. The results indicate 3H, 14C, and 36Cl as the most relevant radionuclides concerning the resultant activity concentrations and estimated dose rates at the site boundary. For this fictive test case, the site boundary is located a distance 250 m downstream of the accelerator, which leads to acceptable risk for the public, given the legal standards.