A pragmatic approach for estimation of source-zone emissions at LNAPL contaminated sites

When considering natural attenuation as a remediation strategy at a site contaminated by a light non-aqueous phase liquid (LNAPL), it is important to consider the emission of contaminants from the source zone. A quantification of source-zone emissions is essential both for comparison with down-gradient mass fluxes to provide an estimate of fractional mass flux reduction, as well as for estimating the source lifetime. Because the spatial distribution of LNAPL at a field site is strongly dependent on both the spill circumstances and the heterogeneity of the geologic materials, which can be problematic for in-situ determination, alternative methods for estimating source-zone emissions are needed. In this work, a three-dimensional multiphase flow and transport modelling approach is used to investigate the relationship between the lateral extent of an LNAPL body and the emission of contaminants to groundwater at a contaminated site. For simulations involving an LNAPL release in an aquifer comprised of heterogeneous porosity and permeability distributions that were generated geostatistically, it is shown that a simple linear relationship exists between the lateral extent of the LNAPL body in the capillary fringe and the emission to the aqueous phase. The parameters describing the relationship are found to be linear functions of the groundwater flow velocity and the vertical infiltration rate. This site-specific relationship provides a simple method to estimate contaminant emissions to groundwater at LNAPL contaminated sites.     

Effect of trichloroethylene (TCE) inhalation on biotransformation enzymes of rat lung and liver

Trichloroethylene (TCE) is widely used as an industrial solvent and cleaning fluid. In the present study the toxic effects of TCE inhalation on pulmonary and hepatic biotransformation enzymes in rats have been investigated by assay of aniline hydroxylase (AH), aminopyrine-N-demethylase (APD), benzo-a-pyrene hydroxylase (BH) and glutathione-s-transferase (GST) activities and glutathione (GSH) contents in liver as well as lungs of exposed animals. In both organs phase I and phase II drug metabolizing enzymes have been found to be increased along with decrease in GSH contents following TCE inhalation. Pulmonary as well as hepatic MFO's seem to be activated by inhaled TCE probably in an attempt for its rapid detoxification and reduced glutathione is used during its biotransformation.