4.7 Article

Plutonium mobilization from contaminated estuarine sediments, Esk Estuary (UK)

期刊

CHEMOSPHERE
卷 308, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.136240

关键词

Plutonium; Contaminated sediments; Irish sea; Plutonium leaching; Redox chemistry; Microbial communities; Anoxic conditions

资金

  1. Office of Science, Biological and Environmental Research, Subsurface Biogeochemical Research program [SCW1053]
  2. U.S. Department of Energy by Lawrence Livermore National Laboratory [DE-AC52-07NA27344]
  3. UK NERC RATE programme [SCW1053]
  4. UK Environment Agency and Radioactive Waste Management Ltd.
  5. Battelle Savannah River Alli-ance, LLC [DE-AC52-07NA27344]
  6. U.S. Department of Energy [NE/L000202/1]
  7. [89303321CEM000080]
  8. [LLNL-JRNL-831425]

向作者/读者索取更多资源

Since 1952, the Sellafield nuclear complex in the UK has been authorized to release liquid radioactive effluent into the Irish Sea, making it the largest source of plutonium (Pu) discharged in western Europe. This study examines the mobility of Pu in contaminated sediments collected from the Esk Estuary and finds that Pu leaching is enhanced under anoxic conditions. These findings provide valuable insights into the stability of Pu in transient environments.
Since 1952, liquid radioactive effluent containing(238-242)Pu, Am-241, Np-237, Cs-137, and Tc-99 has been released with authorization from the Sellafield nuclear complex (UK) into the Irish Sea. This represents the largest source of plutonium (Pu) discharged in all western Europe, with 276 kg having been released. In the Eastern Irish Sea, the majority of the transuranic activity has settled into an area of sediments (Mudpatch) located off the Cumbrian coast. Radionuclides from the Mudpatch have been re-dispersed via particulate transport in fine-grained estuarine and intertidal sediments to the North-East Irish Sea, including the intertidal saltmarsh located at the mouth of the Esk Estuary. Saltmarshes are highly dynamic systems which are vulnerable to external agents (sea level change, erosion, sediment supply, and freshwater inputs), and their stability remains uncertain under current sea level rise projections and possible increases in storm activity. In this work, we examined factors affecting Pu mobility in contaminated sediments collected from the Esk Estuary by conducting leaching experiments under both anoxic and oxic conditions. Leaching experiments were conducted over a 9-month period and were periodically sampled to determine solution phase Pu via multicollector-inductively coupled plasma-mass spectrometry (MC-ICP-MS), and to measure redox indicators (Eh, pH and extractable Fe(II)). Microbial community composition was also characterized in the sediments, and at the beginning and end of the anoxic/oxic experiments. Results show that: 1) Pu leaching is about three times greater in solutions leached under anoxic conditions compared to oxic conditions, 2) the sediment slurry microbial communities shift as conditions change from anoxic to oxic, 3) Pu leaching is enhanced in the shallow sediments (0-10 cm depth), and 4) the magnitude of Pu leached from sediments is not correlated with total Pu, indicating that the biogeochemistry of sediment-associated Pu is spatially heterogeneous. These findings provide constraints on the stability of redox sensitive Pu in biogeochemically dynamic/transient environments on a timescale of months and suggests that anoxic conditions can enhance Pu mobility in estuarine systems.

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