SLAC Study Helps Explain Why Uranium Persists in Groundwater at Former Mining Sites

A recent study led by scientists at the Department of Energy’s SLAC National Accelerator Laboratory helps describe how the contaminant cycles through the environment at former uranium mining sites and why it can be difficult to remove. Contrary to assumptions that have been used for modeling uranium behavior, researchers found the contaminant binds to organic matter in sediments. The findings provide more accurate information for monitoring and remediation at the sites.

The results were published in the Proceedings of the National Academy of Sciences.

In 2014, researchers at SLAC’s Stanford Synchrotron Radiation Lightsource (SSRL) began collaborating with the DOE Office of Legacy Management, which handles contaminated sites associated with the legacy of DOE’s nuclear energy and weapons production activities. Through projects associated with the Uranium Mill Tailings Radiation Control Act, the DOE remediated 22 sites in Colorado, Wyoming and New Mexico where uranium had been extracted and processed during the 1940s to 1970s.

Uranium was removed from the sites as part of the cleanup process, and the former mines and waste piles were capped more than two decades ago. Remaining uranium deep in the subsurface under the capped waste piles was expected to leave these sites due to natural groundwater flow. However, uranium has persisted at elevated levels in nearby groundwater much longer than predicted by scientific modeling.

In an earlier study, the SLAC team discovered that uranium accumulates in the low-oxygen sediments near one of the waste sites in the upper Colorado River basin. These deposits contain high levels of organic matter—such as plant debris and bacterial communities.

During this latest study, the researchers found the dominant form of uranium in the sediments, known as tetravalent uranium, binds to organic matter and clays in the sediments. This makes it more likely to persist at the sites. The result conflicted with current models used to predict movement and longevity of uranium in sediments, which assumed that it formed an insoluble mineral called uraninite.

Different chemical forms of the element vary widely in how mobile they are—how readily they move around—in water, says Sharon Bone, lead author on the paper and a postdoctoral researcher at SSRL, a DOE Office of Science User Facility.

Since the uranium is bound to organic matter in sediments, it is immobile under certain conditions. Tetravalent uranium may become mobile when the water table drops and oxygen from the air enters spaces in the sediment that were formerly filled with water, particularly if the uranium is bound to organic matter in sediments rather than being stored in insoluble minerals.

“Either you want the uranium to be soluble and completely flushed out by the groundwater, or you just want the uranium to remain in the sediments and stay out of the groundwater,” Bone says. “But under fluctuating seasonal conditions, neither happens completely.”

This cycling in the aquifer may result in the persistent plumes of uranium contamination found in groundwater, something that wasn’t captured by earlier modeling efforts.

“For the most part, uranium contamination has only been looked at in very simple model systems in laboratories,” Bone says. “One big advancement is that we are now looking at uranium in its native environmental form in sediments. These dynamics are complicated, and this research will allow us to make field-relevant modeling predictions.”

The study combined the expertise of researchers at SLAC, Pacific Northwest National Laboratory and the Canadian Light Source. The research team used a blend of techniques to analyze samples of sediments in the experiment. They performed X-ray spectroscopy at SSRL to identify the chemical form of uranium. Capabilities at the Canadian Light Source and at the Environmental Molecular Science Laboratory (EMSL) at Pacific Northwest National Laboratory were used to map the locations of the elements in the samples at the nanometer scale. This additional information allowed the researchers to determine whether or not the uranium was bound to carbon-containing, or organic, materials. SSRL and EMSL are DOE Office of Science User Facilities.

The DOE Office of Science funded the project.

Citation: Bone et al., Proceedings of the National Academy of Sciences, 09 January 2017 (doi: 10.1073/pnas.1611918114)

For questions or comments, contact the SLAC Office of Communications at communications@slac.stanford.edu.

SLAC is a multi-program laboratory exploring frontier questions in photon science, astrophysics, particle physics and accelerator research. Located in Menlo Park, Calif., SLAC is operated by Stanford University for the U.S. Department of Energy's Office of Science.

SLAC National Accelerator Laboratory is supported by the Office of Science of the U.S. Department of Energy. The Office of Science is the single largest supporter of basic research in the physical sciences in the United States, and is working to address some of the most pressing challenges of our time. For more information, please visit science.energy.gov.