Radioiodine (129I) poses a risk to the environment due to its long half-life,
toxicity, and mobility. It is found at the U.S. Department of Energy
Hanford Site due to legacy releases of nuclear wastes to the subsurface
where 129I is predominantly present as iodate (IO3
–). To date, a cost-effective and scalable cleanup
technology for 129I has not been identified, with hydraulic
containment implemented as the remedial approach. Here, novel high-performing
sorbents for 129I remediation with the capacity to reduce 129I concentrations to or below the US Environmental Protection
Agency (EPA) drinking water standard and procedures to deploy them
in an ex-situ pump and treat (P&T) system are introduced. This
includes implementation of hybridized polyacrylonitrile (PAN) beads
for ex-situ remediation of IO3
–-contaminated
groundwater for the first time. Iron (Fe) oxyhydroxide and bismuth
(Bi) oxyhydroxide sorbents were deployed on silica substrates or encapsulated
in porous PAN beads. In addition, Fe–, cerium (Ce)–,
and Bi–oxyhydroxides were encapsulated with anion-exchange
resins. The PAN–bismuth oxyhydroxide and PAN–ferrihydrite
composites along with Fe- and Ce-based hybrid anion-exchange resins
performed well in batch sorption experiments with distribution coefficients
for IO3
– of >1000 mL/g and rapid removal
kinetics. Of the tested materials, the Ce-based hybrid anion-exchange
resin was the most efficient for removal of IO3
– from Hanford groundwater in a column system, with 50% breakthrough
occurring at 324 pore volumes. The functional amine groups on the
parent resin and amount of active sorbent in the resin can be customized
to improve the iodine loading capacity. These results highlight the
potential for IO3
– remediation by hybrid
sorbents and represent a benchmark for the implementation of commercially
available materials to meet EPA standards for cleanup of 129I in a large-scale P&T system.
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