Environ. Sci. Technol., 39 (17), 6777 -6785, 2005. 10.1021/es048640f S0013-936X(04)08640-7
Web Release Date: July 30, 2005

Copyright © 2005 American Chemical Society

Reductive Dechlorination of the Vinyl Chloride Surrogate Chlorofluoroethene in TCE-Contaminated Groundwater

Elliot Ennis, Ralph Reed, Mark Dolan, Lewis Semprini, Jonathan Istok, and Jennifer Field,

Department of Chemistry, Department of Environmental and Molecular Toxicology, and Department of Civil, Construction, and Environmental Engineering, Oregon State University, Corvallis, Oregon 97331

Received for review August 31, 2004

Revised manuscript received May 31, 2005

Accepted June 13, 2005

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 preferentially transformed 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 M/day, while the in situ rates of E-CFE disappearance ranged from 0.17 to 0.99 M/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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