A soil radon-deficit survey was carried out in a site polluted with kerosene (Rome, Italy) in winter 2016 to assess the contamination due to the NAPL residual component in the vadose zone and to investigate the role of the vapor plume. Radon is indeed more soluble in the residual NAPL than in air or water, but laboratory experiments demonstrated that it is also preferentially partitioned in the NAPL vapors that transport it and may influence soil radon distribution patterns. Specific experimental configurations were designed and applied to a 31-station grid to test this hypothesis; two RAD7 radon monitors were placed in-series and connected to the top of a hollow probe driven up to 80-cm depth; the first instrument was directly attached to the probe and received humid soil gas, which was counted and then conveyed to the second monitor through a desiccant (drierite) cylinder capturing moisture and eventually the NAPL volatile component plus the radon dissolved in vapors. The values from the two instruments were cross-calibrated through specifically designed laboratory experiments and compared. The results are in agreement within the error range, so the presence of significant NAPL vapors, eventually absorbed by drierite, was ruled out. This is in agreement with low concentrations of soil VOCs. Accordingly, the radon-deficit is ascribed to the residual NAPL in the soil pores, as shown very well also by the obtained maps. Preferential areas of radon-deficit were recognised, as in previous surveys. An average estimate of 21 L (17 Kg) of residual NAPL per cubic meter of terrain is provided on the basis of original calculations, developed from published equations. A comparison with direct determination of total hydrocarbon concentration (23 kg per cubic meter of terrain) is provided.
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http://dx.doi.org/10.1016/j.jenvrad.2017.02.014 | DOI Listing |
Water Res
December 2024
BRGM (French Geological Survey), Orléans 45060, France.
Polymer solution injection has emerged as a promising method for the remediation of NAPL (non-aqueous phase liquids)-contaminated aquifers. This technique enhances recovery efficiency by modifying viscous forces, stabilizing the displacement front, and minimizing channeling effects. However, there remains a significant gap in understanding the behavior of polymer solutions, particularly those with different molecular weights (MW), for mobilizing DNAPL (dense non-aqueous phase liquids) trapped in heterogeneous aquifers, especially within low-permeability layers.
View Article and Find Full Text PDFJ Hazard Mater
January 2024
Environmental Science Department, University of Arizona, Tucson, AZ, USA; Hydrology and Atmospheric Sciences Department, University of Arizona, Tucson, AZ, USA. Electronic address:
The objective of this research was to examine the influence of nonuniform NAPL distribution and hydraulic-conductivity heterogeneity on the retention and transport of PFAS. Two-dimensional flow cell experiments were conducted to investigate the impact of NAPL configuration on PFOS retention. Two simplified NAPL configurations were used, one with decane present as residual and the other with greater-than-residual (pool) NAPL saturation.
View Article and Find Full Text PDFGround Water
November 2023
Anchor QEA, LLC, San Francisco, CA, USA.
Groundwater professionals require methods to estimate the potential time required to achieve remedial goals, including locations within and downgradient of zones containing nonaqueous phase liquids (NAPLs). NAPLs have long been recognized as persistent contaminant sources to groundwater. Dissolution of multicomponent NAPLs is particularly complex, and numerical models that explicitly simulate it are not widely available.
View Article and Find Full Text PDFJ Hazard Mater
May 2023
Department of Civil & Environmental Engineering, University of Waterloo, Ontario, Canada.
An experimental and computational investigation of in situ chemical oxidation (ISCO) of weathered diesel fuel in soil columns was undertaken to validate a reactive-transport model capable of predicting contaminant mass reduction from a residual source zone. Reactivity tests with contaminated groundwater in batch reactors were used to estimate a priori the kinetic parameters of a phenomenological model of the oxidation of petroleum hydrocarbon (PHC) mixture fractions. The transport model, which incorporated groundwater flow, dissolution of main PHC fractions, and homogeneous reaction in the aqueous phase, was subsequently validated against experimental data of ISCO in soil columns using repetitive treatments with unactivated and alkaline-activated persulfate.
View Article and Find Full Text PDFChemosphere
December 2022
Chevron Technical Center, 6001 Bollinger Canyon Road, San Ramon, CA, 94583, USA.
Several types of laboratory experiments were conducted to evaluate isotope fractionation caused by phase transfer process for a selection of common environmental contaminants. Carbon and hydrogen isotope fractionation caused by vaporization of non-aqueous phase liquid (NAPL), by volatilization from water and by dissolution into an organic solvent (tetraethylene glycol dimethylether or TGDE) under equilibrium conditions was investigated with closed system experimental setups to isolate the air-liquid partitioning process. A selection of aromatic, aliphatic and chlorinated compounds along with one fuel oxygenate (methyl tert-butyl ether or MTBE) were evaluated to determine isotope enrichment factor related to respective phase transfer process.
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