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An Evaluation of Some Systems for Sampling Gas-Charged Ground Water for Volatile Organic Analysis
Authors:JF Barker  R Dickhout
Institution:James Barker is an associate professor in the Department of Earth Sciences (University of Waterloo, Waterloo, Ontario, Canada N2L 3G1) and a member of the Institute of Groundwater Research at the University of Waterloo. His research interests are contaminant hydrogeology, particularly the behavior of organic contaminants and their biotransformations, the geochemistry of organic-metal interactions, and the origin and geochemistry of petroleum and natural gas resources.;Ralph Dickhout is the head of the Organic Geochemistry Laboratory in the Department of Earth Sciences (University of Waterloo, Waterloo, Ontario, Canada N2L 3G1). He graduated from the University of Waterloo in 1978 with an Honours B.Sc. in applied chemistry. He has been developing analytical techniques and supervising analyses in support of a broad range of organic geochemical projects, including petroleum and oil shale studies and organic contaminant behavior in ground water.
Abstract:Loss of volatile organics during sampling is a well-recognized source of bias in ground water monitoring; sampling protocols attempt to minimize such loss. Such bias could be enhanced for ground water highly charged with dissolved gases such as methane. Such ground water was the object of this study. A positive-displacement bladder pump, a momentum-lift pump and a suction-lift, peristaltic pump were employed in sampling both methane-charged ground water for volatile aromatic hydrocarbons and a CO2-charged reservoir water for volatile chlorinated hydrocarbons. In both cases, the suction-lift pump produced samples with a significant negative bias (9 to 33 percent) relative to the other methods. Little difference between samples produced by the other pump Systems was noted at the field site, but in sampling the reservoir, the bladder pump produced samples that were 13 to 19 percent lower in halocarbon concentration than were samples from the momentum-lift pump.
These negative biases are tentatively interpreted as losses due to volatilization during sampling. Slightly greater negative biases occur for compounds of higher volatility as estimated from their Henry's law constants. Additional studies appear to be warranted in order to adequately establish the scientific basis for recommending protocols for sampling ground water in which degassing could enhance the loss of volatile organics during sampling.
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