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Equilibrium partitioning of PCB congeners in the water column: Field measurements from the Hudson River

The environmental behavior of hydrophobic organic compounds in water is driven by partitioning between dissolved and sorbed phases. Partitioning behavior of a compound is often based on empirical relationships to other properties of the chemical, such as water solubility and octanol-water partition...

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Bibliographic Details
Published in:Chemosphere (Oxford) 1998-06, Vol.36 (15), p.3149-3166
Main Authors: Butcher, J.B., Garvey, E.A., Bierman, V.J.
Format: Article
Language:English
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Summary:The environmental behavior of hydrophobic organic compounds in water is driven by partitioning between dissolved and sorbed phases. Partitioning behavior of a compound is often based on empirical relationships to other properties of the chemical, such as water solubility and octanol-water partition coefficients, but actual partitioning in the environment may differ significantly from such predictions. We conducted intensive studies of the distribution of PCBs in the fresh water portion of the Hudson River, using sensitive capillary-column gas chromatography methods to calibrate and resolve quantitations for 90 PCB congeners in 48 samples at 10 locations. A linear equilibrium model of PCB congener partitioning, when corrected for temperature and suspended-matter organic carbon content, provides a good representation of phase distribution. When particulate-phase concentrations are predicted from dissolved concentrations with a two-phase model, the predictions are unbiased for the majority of samples and the average percent difference between observed and predicted particulate concentrations is ±43 percent. Estimated in situ partition coefficients show systematic differences from partition coefficients predicted from octanol-water partitioning. Partitioning to colloids appears to be a significant component of total concentration for mono- and dichlorobiphenyls, but not for more highly chlorinated congeners.The colloidal fraction may still cause significant overestimation of the bioavailable fraction for more hydrophobic congeners when a two-component model is used.
ISSN:0045-6535
1879-1298
DOI:10.1016/S0045-6535(98)00015-0