Journal
SCIENCE OF THE TOTAL ENVIRONMENT
Volume 757, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.scitotenv.2020.143818
Keywords
Radionuclides; Montmorillonite colloids; Carbonate rocks; Reactive transport
Categories
Funding
- Israeli Atomic Energy Agency, PAZY [287/17]
- Israel Science Foundation [165/17]
- U.S. Department of Energy by Lawrence Livermore National Laboratory [DE-AC52-07NA27344]
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This study investigated the influence of montmorillonite colloids on the mobility of Pu-238, U-233, and Cs-137 through a chalk fracture. The results showed that uranium sorbed sparingly to chalk, while cesium sorbed strongly to both the montmorillonite colloids and chalk, resulting in low Cs-137 breakthrough. The experiments revealed differences in Pu(IV) and Pu(V) transport behavior, highlighting the importance of understanding redox-sensitive radionuclide migration.
The influence of montmorillonite colloids on the mobility of Pu-238, U-233 and Cs-137 through a chalk fracture was investigated to assess the transport potential for radioactive waste. Radioisotopes of each element, along with the conservative tracer tritium, were injected in the presence and absence of montmorillonite colloids into a naturally fractured chalk core. In parallel, batch experiments were conducted to obtain experimental sorption coefficients (K-d, mL/g) for both montmorillonite colloids and the chalk fracture material. Breakthrough curves were modelled to determine diffusivity and sorption of each radionuclide to the chalk and the colloids under advective conditions. Uranium sorbed sparingly to chalk (log K-d = 0.7 +/- 0.2) in batch sorption experiments. U-233(VI) breakthrough was controlled primarily by the matrix diffusion and sorption to chalk (15 and 25% recovery with and without colloids, respectively). Cesium, in contrast, sorbed strongly to both the montmorillonite colloids and chalk (batch log K-d = 3.2 +/- 0.01 and 3.9 +/- 0.01, respectively). The high affinity to chalk and low colloid concentrations overwhelmed any colloidal Cs transport, resulting in very low Cs-137 breakthrough (1.1-5.5% mass recovery). Batch and fracture transport results, and the associated modelling revealed that Pu migrates both as Pu (IV) sorbed to montmorillonite colloids and as dissolved Pu(V) (7% recovery). Transport experiments revealed differences in Pu(IV) and Pu(V) transport behavior that could not be quantified in simple batch experiments but are critical to effectively predict transport behavior of redox-sensitive radionuclides. Finally, a brackish groundwater solution was injected after completion of the fracture flow experiments and resulted in remobilization and recovery of 2.2% of the total sorbed radionuclides which remained in the core from previous experiments. In general, our study demonstrates consistency in sorption behavior between batch and advective fracture transport. The results suggest that colloid-facilitated radionuclide transport will enhance radionuclide migration in fractured chalk for those radionuclides with exceedingly high affinity for colloids. (C) 2020 Elsevier B.V. All rights reserved.
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