Magnetic resonance imaging of nonaqueous phase liquid during soil vapor extraction in heterogeneous porous media

Soil vapor extraction (SVE) is commonly used to remediate nonaqueous phase liquids (NAPLs) from the vadose zone. This paper aims to determine the effect of grain size heterogeneity on the removal of NAPL in porous media during SVE. Magnetic resonance imaging (MRI) was used to observe and quantify the amount and location of NAPL in flow-through columns filled with silica gel grains. MRI is unique because it is nondestructive, allowing three-dimensional images to be taken of the phases as a function of space and time. Columns were packed with silica gel in three ways: coarse grains (250-550 microm) only, fine grains (32-63 microm) only, and a core of fine grains surrounded by a shell of coarse grains. Columns saturated with water were drained under a constant suction head, contaminated with decane, and then drained to different decane saturations. Each column was then continuously purged with water-saturated nitrogen gas and images were taken intermittently. Results showed that at residual saturation, a sharp volatilization front moved through the columns filled with either coarse-grain or fine-grain silica gel. In the heterogeneous columns, the volatilization front in the core lagged just behind the shell because gas flow was greater through the shell and decane in the core diffused outward to the shell. When decane saturation in the core was above residual saturation, decane volatilization occurred near the inlet, the relative decane saturation throughout the core dropped uniformly, and decane in the core flowed in the liquid phase to the shell to replenish volatilized decane. These results indicate that NAPL trapped in low-permeability zones can flow to replenish areas where NAPL is lost due to SVE. However, when residual NAPL saturation is reached, NAPL flow no longer occurs and diffusion limits removal from low-permeability zones.     

Field intercomparison of throughfall measurements performed within the framework of the Pan European intensive monitoring program of EU/ICP Forest

A 6-month field intercomparison study on throughfall measurements was performed at Speulder forest near the west coast in The Netherlands. Twenty throughfall sampling systems were evaluated on accuracy, sampling strategy and performance under field conditions. Throughfall fluxes of NO3-, K+ and Kjeldahl-N generally could be determined with a larger accuracy than fluxes of SO4(2-), NH4+, Na+, Cl-, Mg2+, Ca2+, and alkalinity. Throughfall fluxes of H+ generally had the lowest accuracy. Only 20% of the sampling systems differed more than 20% from the best estimate, whereas 45% of the systems stayed within a 10% range from the best estimate. The difference from the best estimate was mainly caused by aspects related to sampling strategy, like, for example, collecting area, sampler placement. The inaccuracy induced by the sampling system appeared to be much larger than that resulting from the analysis of the samples by different laboratory as determined by ring-tests. The field intercomparison described in this article gave a good insight in the different aspects contributing to the overall accuracy of the measurements. However, performing a future field intercomparison is recommended for throughfall and stemflow in order to also take in account other aspects that might influence the performance of the different measurement systems (e.g. tree species, climate zone, summer/winter period).     

Laser-induced fluorescence and fast gas chromatography/mass spectrometry with subsurface thermal extraction of organics: Field analytical technologies for expediting site characterization and cleanup

This article describes new field-based technologies that support the Dynamic Workplan/Adaptive Sampling and Analysis Program employed to better characterize hazardous waste sites at lower cost. A laser-induced fluorescence (LIF) probe was designed and field-tested with a cone penetrometer (CP) for investigating petroleum contaminants present at under-ground tank farms. The LIF produced real-time quantitative data for naphthalene and semiquantitative results for total petroleum hydrocarbons and diesel range organics. Two different projects are described employing fast gas chromatography/mass spectrometry (GC/MS) in the field. A 70-foot heated transfer line and probe were used in combination with a cone penetrometer to thermally extract (TE) subsurface soil-bound semivolatile organics. In the second project, soil samples were collected by a Geoprobe^TM and brought to the surface for analysis. The direct measurement TECP data produced semiquantitative results while the more conventional means of collecting and analyzing samples produced risk analysis quality data in the field. A new set of mass spectrometry algorithms provided the technology breakthrough for identifying and quantifying a wide range of Environmental-Protection-Agency-listed target compounds in the presence of high levels of matrix (petroleum) interferents under fast, 7 min/sample, GC conditions.