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Long-term diffusion of U(VI) in bentonite: Dependence on density
Claudia Joseph1, Jens Mibus2, Paul Trepte2
1Glenn T. Seaborg Institute, Physical & Life Sciences Directorate, Lawrence Livermore National Laboratory, L-231, P.O. Box 808, Livermore, CA 94550, USA.
The Science of the Total Environment
|October 15, 2016
Summary
Uranium diffusion in MX-80 bentonite was studied for six years. Long-term in-diffusion of uranium was unexpectedly slow, suggesting processes impacting nuclear waste repository safety.
Area of Science:
- Geochemistry
- Nuclear Engineering
- Materials Science
Background:
- Nuclear waste repositories require robust safety assessments.
- MX-80 bentonite is a potential buffer material for repositories.
- Understanding uranium (U(VI)) transport in bentonite is crucial for safety.
Purpose of the Study:
- Investigate U(VI) diffusion in MX-80 bentonite over six years.
- Determine the impact of clay dry density on U(VI) diffusion.
- Compare long-term in-diffusion with short-term experimental results.
Main Methods:
- Performed in- and out-diffusion experiments with U(VI) in MX-80 bentonite at three dry densities (1.3, 1.6, 1.9 g/cm³).
- Utilized synthetic MX-80 model pore water as the background electrolyte.
- Analyzed U(VI) diffusion depths and calculated effective (De) and apparent (Da) diffusion coefficients.
Main Results:
- U(VI) diffusion depth decreased with increasing dry density (3mm at 1.3 g/cm³ to 1mm at 1.9 g/cm³).
- No through-diffusion of U(VI) tracer was observed; natural uranium leaching occurred.
- Long-term in-diffusion Da values were two orders of magnitude lower than short-term results, suggesting reduced effective porosity.
Conclusions:
- Increasing dry density significantly reduces U(VI) diffusion in MX-80 bentonite.
- Long-term U(VI) in-diffusion is slower than predicted by short-term experiments, possibly due to speciation changes or altered porosity.
- Long-term studies are essential for accurately assessing nuclear waste repository safety.
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