6 research outputs found
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Evidence of Remediation-Induced Alteration of Subsurface Poly- and Perfluoroalkyl Substance (PFAS) Distribution at a Former Firefighter Training Area
Poly- and perfluoroalkyl substances (PFASs) are a class of fluorinated chemicals that are utilized in firefighting and have been reported in groundwater and soil at several firefighter training areas. In this study, soil and groundwater samples were collected from across a former firefighter training area to examine the extent to which remedial activities have altered the composition and spatial distribution of PFASs in the subsurface. Log K[subscript oc] values for perfluoroalkyl acids (PFAAs), estimated from analysis of paired samples of groundwater and aquifer solids, indicated that solid/water partitioning was not entirely consistent with predictions based on laboratory studies. Differential PFAA transport was not strongly evident in the subsurface, likely due to remediation-induced conditions. When compared to the surface soil spatial distributions, the relative concentrations of perfluorooctane sulfonate (PFOS) and PFAA precursors in groundwater strongly suggest that remedial activities altered the subsurface PFAS distribution, presumably through significant pumping of groundwater and transformation of precursors to PFAAs. Additional evidence for transformation of PFAA precursors during remediation included elevated ratios of perfluorohexane sulfonate (PFHxS) to PFOS in groundwater near oxygen sparging wells
Metal Release from Sandstones under Experimentally and Numerically Simulated CO<sub>2</sub> Leakage Conditions
Leakage
of CO<sub>2</sub> from a deep storage formation into an
overlying potable aquifer may adversely impact water quality and human
health. Understanding CO<sub>2</sub>-water-rock interactions is therefore
an important step toward the safe implementation of geologic carbon
sequestration. This study targeted the geochemical response of siliclastic
rock, specifically three sandstones of the Mesaverde Group in northwestern
Colorado. To test the hypothesis that carbonate minerals, even when
present in very low levels, would be the primary source of metals
released into a CO<sub>2</sub>-impacted aquifer, two batch experiments
were conducted. Samples were reacted for 27 days with water and CO<sub>2</sub> at partial pressures of 0.01 and 1 bar, representing natural
background levels and levels expected in an aquifer impacted by a
small leakage, respectively. Concentrations of major (e.g., Ca, Mg)
and trace (e.g., As, Ba, Cd, Fe, Mn, Pb, Sr, U) elements increased
rapidly after CO<sub>2</sub> was introduced into the system, but did
not exceed primary Maximum Contaminant Levels set by the U.S. Environmental
Protection Agency. Results of sequential extraction suggest that carbonate
minerals, although volumetrically insignificant in the sandstone samples,
are the dominant source of mobile metals. This interpretation is supported
by a simple geochemical model, which could simulate observed changes
in fluid composition through CO<sub>2</sub>-induced calcite and dolomite
dissolution
Evidence of Remediation-Induced Alteration of Subsurface Poly- and Perfluoroalkyl Substance Distribution at a Former Firefighter Training Area
Poly- and perfluoroalkyl substances
(PFASs) are a class of fluorinated
chemicals that are utilized in firefighting and have been reported
in groundwater and soil at several firefighter training areas. In
this study, soil and groundwater samples were collected from across
a former firefighter training area to examine the extent to which
remedial activities have altered the composition and spatial distribution
of PFASs in the subsurface. Log <i>K</i><sub>oc</sub> values
for perfluoroalkyl acids (PFAAs), estimated from analysis of paired
samples of groundwater and aquifer solids, indicated that solid/water
partitioning was not entirely consistent with predictions based on
laboratory studies. Differential PFAA transport was not strongly evident
in the subsurface, likely due to remediation-induced conditions. When
compared to the surface soil spatial distributions, the relative concentrations
of perfluorooctanesulfonate (PFOS) and PFAA precursors in groundwater
strongly suggest that remedial activities altered the subsurface PFAS
distribution, presumably through significant pumping of groundwater
and transformation of precursors to PFAAs. Additional evidence for
transformation of PFAA precursors during remediation included elevated
ratios of perfluorohexanesulfonate (PFHxS) to PFOS in groundwater
near oxygen sparging wells
Nitrogen Fate and Transport in a Conventional Onsite Wastewater Treatment System Installed in a Clay Soil: A Nitrogen Chain Model
Nitrogen cycling in clay-textured soils with onsite wastewater treatment systems is studied and modeled much less often than sand- and loam-textured soils because there is little data on onsite wastewater treatment system performance in these soils. An N chain model with water-content dependent first-order transformation rates for nitrification and denitrification was developed and calibrated using data from a conventional onsite wastewater treatment system installed in a clay-textured soil. The model predicted the N removal in the system. Estimates of N loss were specific to clay-textured soils and should be valuable to TMDL developers who need to predict load allocations for non-point sources in the Piedmont. Nitrogen cycling in clay-textured soils with onsite wastewater treatment systems (OWTS) is studied and modeled much less often than sand- and loam-textured soils because there is little data on OWTS performance in these soils. Information on the nitrogen loads from these systems is needed for quantification of total maximum daily loads (TMDLs). The objective of this study was to calibrate a 2D HYDRUS model using experimental soil pressure head and vadose zone nitrogen (N) and chloride (Cl) data from a conventional OWTS that was installed in a clay soil in the Piedmont region of Georgia. An N chain model with water-content dependent first-order transformation rates for nitrification and denitrification was developed. The overall predicted soil pressure heads and solute concentrations were similar to data collected from the field experiment. The calibrated model made it possible to estimate water and solute fluxes in the drainfield and N losses from the OWTS. The estimated annual N loss from leaching at the lower boundary of the experimental drainfield was 3.8 kg yr-1. Scaled up to an OWTS size typical for GA and a zoning density of 5 homes ha-1, the N load to groundwater would be 57.4 kg ha-1 yr-1, which is comparable to agricultural production losses to groundwater. The model predicted 52% of the N removal in the system was from denitrification, whereas plant uptake and change in N storage accounted for ≤5% of the N loss. These estimates were specific to clay-textured soils and should be valuable to TMDL developers who need to predict load allocations for nonpoint sources in the Piedmont. © Soil Science Society of America 5585 Guilford Rd., Madison, WI 53711 USA. All rights reserved