Publications by authors named "Stanley Feenstra"

Article Synopsis
  • The study investigated how different types of carbon-rich materials (thermally altered carbonaceous matter) affect the absorption of trichloroethylene (TCE) in an alluvial aquifer with low organic carbon content.
  • Results showed that the main component affecting TCE sorption was a combination of kerogen and black carbon, which made up a large portion of the sediment, particularly in different-sized particles like sands and silts.
  • Findings indicated that the nonlinear nature of TCE sorption enhances its persistence in the groundwater and suggests that similar processes might occur in other areas with comparable geological features.
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Pump-and-treat (P&T) remediation and associated concentration tailing are investigated at the field scale in a mildly heterogeneous sandy aquifer through the extraction of dissolved chlorinated solvent plumes that had developed over 475 d from a multicomponent dense nonaqueous-phase liquid (DNAPL) source intentionally emplaced in the aquifer at the Borden (ON) research site. Extraction was accomplished via a source-containment well located 25 m from the source and two further downgradient plume-centerline wells to remove the advancing high-concentration dissolved plumes. The 550 days of detailed P&T field data demonstrated the following: remediation, albeit slowly, of the leading 25-60 m plume section to around typical drinking water standard concentrations; concentration tailing (reduction) over 4 orders of magnitude in the plume; a steady-state concentration "plateau" in the source-containment well capturing the steadily dissolving DNAPL source; influences of extraction rate changes (concentration rebounds); and, lengthy tailing from inter-well stagnation-zone areas.

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Field-scale dissolution of a multicomponent DNAPL (dense nonaqueous-phase liquid) source intentionally emplaced below the water table is evaluated in a well-characterized natural aquifer setting. The block-shaped source contained 23 kg of a trichloromethane, trichloroethene, and perchloroethene mixture homogeneously distributed at 5% saturation of pore space. Dissolution was monitored for 3 yr via down-gradient samplers (1-m fence) and occasional intra-source sampling.

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