posted on 2019-06-13, 00:00authored byMavrik Zavarin, Pihong Zhao, Claudia Joseph, James D. Begg, Mark A. Boggs, Zurong Dai, Annie B. Kersting
Approximately 2.8 t of plutonium
(Pu) has been deposited in the
Nevada National Security Site (NNSS) subsurface as a result of underground
nuclear testing. Most of this Pu is sequestered in nuclear melt glass.
However, Pu migration has been observed and attributed to colloid
facilitated transport. To identify the mechanisms controlling Pu mobilization,
long-term (∼3 year) laboratory nuclear melt glass alteration
experiments were performed at 25 to 200 °C to mimic hydrothermal
conditions in the vicinity of underground nuclear tests. The clay
and zeolite colloids produced in these experiments are similar to
those identified in NNSS groundwater. At 200 °C, maximum Pu and
colloid concentrations of 30 Bq/L and 150 mg/L, respectively, were
observed. However, much lower Pu and colloid concentrations were observed
at 25 and 80 °C. These data suggest that Pu concentrations above
the drinking water Maximum Contaminant Levels (0.56 Bq/L) may exist
during early hydrothermal conditions in the vicinity of underground
nuclear tests. However, formation of colloid-associated Pu will tend
to decrease with time as nuclear test cavity temperatures decrease.
Furthermore, median colloid concentrations in NNSS groundwater (1.8
mg/L) suggest that the high colloid and Pu concentrations observed
in our 140 and 200 °C experiments are unlikely to persist in
downgradient NNSS groundwater. While our experiments did not span
all groundwater and nuclear melt glass conditions that may be present
at the NNSS, our results are consistent with the documented low Pu
concentrations in NNSS groundwater.