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Updated: Aug 15, 2026

Development of Sulfidogenic Sludge from Marine Sediments and Trichloroethylene Reduction in an Upflow Anaerobic Sludge Blanket Reactor
Published on: October 15, 2015
Reductive dechlorination of the vinyl chloride surrogate chlorofluoroethene in TCE-contaminated groundwater
Elliot Ennis1, Ralph Reed, Mark Dolan
1Department of Chemistry, Department of Environmental and Molecular Toxicology, and Department of Civil, Construction, and Environmental Engineering, Oregon State University, Corvallis, Oregon 97331, USA.
Abstract:
At many trichloroethene (TCE)-contaminated field sites, microbial transformation of TCE results in the accumulation of vinyl chloride (VC), a known carcinogen and neurotoxin. Quantitative tools are needed to determine the in situ rates of VC transformation to ethene in contaminated groundwater. For this study, E-/Z-chlorofluoroethene (E-/Z-CFE) was evaluated as a surrogate for VC in laboratory microcosm and field push-pull tests. Single-well push-pull tests were conducted at a TCE-contaminated field site by injecting E-/Z-CFE and monitoring for the formation of fluoroethene (FE) over a period of up to 80 days. The rates for VC transformation to ethene and E-CFE transformation to FE were within a factor of 2.7 for laboratory microcosm systems and all preferentiallytransformed E-CFE over Z-CFE. In the field, the in situ rates of FE production from injected E-CFE ranged from 0.0018 to 1.15 microM/day, while the in situ rates of E-CFE disappearance ranged from 0.17 to 0.99 microM/day. No significant Z-CFE transformation was observed in field tests, which indicated preferential utilization of E-CFE over Z-CFE under in situ field conditions. The results of this study indicate E-CFE as a potential surrogate for estimating the in situ rates of VC transformation.
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