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Distribution and Retention of <sup>137</sup>Cs in Sediments at the Hanford Site, Washington
113
Citations
26
References
2001
Year
Hanford SiteSedimentary RecordEngineeringTrace Element GeochemistrySedimentary GeologyMineral ProcessingEarth ScienceSorbed 137Cs+Organic GeochemistryEnvironmental ChemistrySediment AnalysisGeochronologyBiogeochemistrySediment QualitySediment-water InteractionAdsorbed 137Cs+GeologySedimentologyLeaky SstSediment TransportEnvironmental RadiochemistryClay MineralEnvironmental EngineeringEnvironmental RemediationSediment ProcessGeochemistryEnvironmental Toxicology
137Cesium and other contaminants have leaked from single-shell storage tanks (SSTs) into coarse-textured, relatively unweathered unconsolidated sediments. Contaminated sediments were retrieved from beneath a leaky SST to investigate the distribution of adsorbed 137Cs+ across different sediment size fractions. All fractions contained mica (biotite, muscovite, vermiculatized biotite), quartz, and plagioclase along with smectite and kaolinite in the clay-size fraction. A phosphor-plate autoradiograph method was used to identify particular sediment particles responsible for retaining 137Cs+. The Cs-bearing particles were found to be individual mica flakes or agglomerated smectite, mica, quartz, and plagioclase. Of these, only the micaceous component was capable of sorbing Cs+ strongly. Sorbed 137Cs+ could not be significantly removed from sediments by leaching with dithionite citrate buffer or KOH, but a fraction of the sorbed 137Cs+ (5-22%) was desorbable with solutions containing an excess of Rb+. The small amount of 137Cs+ that might be mobilized by migrating fluids in the future would likely sorb to nearby micaceous clasts in downgradient sediments.
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