Uranium
recovery from seawater has been investigated for several
decades for the purpose of securing nuclear fuel for energy production.
In this study, field column experiments have been performed at the
Marine Sciences Laboratory of the Pacific Northwest National Laboratory
(PNNL) using a laboratory-proven, amidoxime-based polymeric adsorbent
developed at the Oak Ridge National Laboratory (ORNL). The adsorbent
was packed either in in-line filters or in flow-through columns. The
maximum amount of uranium uptake from seawater was 3.3 mg of U/g of
adsorbent after 8 weeks of contact between the adsorbent and seawater.
This uranium adsorption amount was about 3 times higher than the maximum
amount achieved in this study by a leading adsorbent developed at
the Japan Atomic Energy Agency (JAEA). Both adsorbents were tested
under similar conditions. The results were used to update an assessment
of the cost of large-scale recovery of uranium from seawater using
the ORNL adsorbent. The updated uranium production cost was estimated
to be reduced to $610/kg of U, approximately half the cost estimated
for the JAEA technology.
A new family of high-surface-area polyethylene fiber adsorbents named the AF series was recently developed at the Oak Ridge National Laboratory (ORNL). The AF series adsorbents were synthesized by radiation-induced graft polymerization of acrylonitrile and itaconic acid (at different monomer/comonomer mol ratios) onto high surface area polyethylene fibers. The degree of grafting (%DOG) of AF series adsorbents was found to be 154−354%. The grafted nitrile groups were converted to amidoxime groups by treating with hydroxylamine. The amidoximated adsorbents were then conditioned with 0.44 M KOH at 80 °C followed by screening at ORNL with sodium-based synthetic aqueous solution, spiked with 8 ppm uranium. The uranium adsorption capacity in simulated seawater screening ranged from 170 to 200 g-U/kg-ads irrespective of %DOG. A monomer/comonomer molar ratio in the range of 7.57−10.14 seemed to be optimum for highest uranium loading capacity. Subsequently, the adsorbents were also tested with natural seawater at Pacific Northwest National Laboratory (PNNL) using flow-through column experiments to determine uranium loading capacity with varying KOH conditioning times at 80 °C. The highest adsorption capacity of AF1 measured after 56 days of marine testing was demonstrated as 3.9 g-U/kg-adsorbent and 3.2 g-U/kg-adsorbent for 1 and 3 h of KOH conditioning at 80 °C, respectively. Based on capacity values of several AF1 samples, it was observed that changing KOH conditioning from 1 to 3 h at 80 °C resulted in a 22−27% decrease in uranium adsorption capacity in seawater.
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