A spill of JP‐4 jet fuel at the U.S. Coast Guard Air Station in Traverse City, Michigan, contaminated a water‐table aquifer. An infiltration gallery (30 ft × 30 ft) was installed above a section of the aquifer containing 700 gal JP‐4. Purge wells recirculated three million gallons of ground water per week through the infiltration gallery at a rate designed to raise the water table above the contaminated interval. Ground water containing ambient concentrations of oxygen and nitrate was first recirculated for 40 days. Concentrations of benzene in monitoring wells beneath the infiltration gallery were reduced from 760 to <1μ/1. Concentrations of toluene, ethylbenzene, m,p‐xylene, and o‐xylene were reduced from 4500 to 17, 840 to 44, 2600 to 490, and 1400 to 260 μ/1, respectively. Average core concentrations of benzene, toluene, ethylbenzene, m,p‐xylene, and o‐xylene were reduced from 0.84 to 0.032, 33 to 0.13, 18 to 0.36, 58 to 7.4, and 26 to 3.2 mg/kg, respectively. Ground water amended with nitrate (10 mg/1 nitrate‐nitrogen) and nutrients was then recirculated for 76 days. Final core concentrations of benzene, toluene, ethylbenzene, m,p‐xylene, and o‐xylene were 0.017,0.036,0.019,0.059, and 0.27 mg/kg, respectively. Final aqueous concentrations were <1 μ/1 for benzene and toluene, 6 μ/1 for ethylbenzene, and 20 to 40 μ/1 for the xylene isomers, in good agreement with predicted values based on residual fuel content and partitioning theory. Although alkylbenzene concentrations have been substantially reduced, the test plot is still contaminated with the weatheredfuel. Based on stoichiometry, approximately 10 times more nitrate was consumed than could be accounted for by BTX degradation alone, indicating that other compounds were also degraded under denitrifying conditions.
Beginning in 1952, waste materials, including volatile organic compounds (VOCs)contaminated with transuranic radionuclides, were generated during the fabrication, assembly, and processing of nuclear weapons components in the US Department of Energy (DOE) weapons productions complex at the Rocky Flats Plant (RFP). Following processing and containerization, drums were shipped to the Subsurface Disposal Area (SDA) at the Idaho National Engineering and Environmental Laboratory (INEEL). During 1968 approximately 9,691 drums were buried there.In subsequent years, observations made during drum retrieval studies indicated that many of the drums were compromised on impact or suffered physical damage by compaction equipment shortly after burial. Corrosion also appears significant on drums buried for a few years. A large vadose-zone contaminant plume composed of solvents buried in the drums has been found beneath the burial area.Phase partitioning calculations show it unlikely that separate-phase solvent has leaked from the compromised drums deep into the soil profile or that solvents have dissolved into infiltrating water. Rather, it appears that the solvents are evaporating out of the barrels into the air phase and further partitioning from there throughout the subsurface.This paper describes the history of mixed wastes buried at the SDA, phase partitioning, and preliminary computer simulation results on gas contaminant mobility in the vadose zone.
No abstract
A numerical model was developed to describe the fate and transport of hydrazinium (N2H5+) and competing Ca2+ and H+ cations applied in acidic solutions to columns of Ca2+/H+-saturated sandy soil during steady saturated flow conditions. Instantaneous ternary H+-Ca2+-N2H5+ cation exchange using the Gaines-Thomas approach was combined with second-order, irreversible, kinetic chemisorption of exchange-phase N2H5+ ions as major retention mechanisms for N2H5+. Exchange-mediated chemisorption is assumed to occur as chemical binding of N2H5+ ions located on carboxyl-group exchange sites to nearby carbonyl groups, consequently decreasing the effective soil cation exchange capacity (CEC). Comparison of simulated and observed breakthrough curves (BTCs) for concentrations of N2H5+ and Ca2+ ions in column effluent was used in model evaluation. The cation transport model with cation exchange coupled with exchange-mediated chemisorption provided a valid first approximation for N2H5+ transport.
No abstract
Field and laboratory studies have been underway at the INEEL and BYU to investigate the effect of atmospheric pressure fluctuations on the migration of contaminant plumes.In the field, two vadose-zone piezometer nests were instrumented to measure soil-pressures and carbon tetrachloride concentrations at depths of roughly 78-ft, 112-ft., and 150-ft., below ground surface in wells 25-ft. apart. At land surface, a manifold was constructed to systematically rotate from port to port at 15-minute increments of time. Contaminant concentrations were measured at each rotation, and soil pressures were measured at all ports at 15-minute increments. Atmospheric pressures were also recorded. Results showed that atmospheric pressure changes propagated downward lagged in time and dampened in amplitude. Carbon tetrachloride concentrations were observed to decrease with pressure increases at each port, suggesting that pressure increases pushed the plume downward. Increases in concentration were observed with decreases in pressure. Concentrations were observed to change at a port by as much as an order of magnitude. Modeling is underway to assist in isolating the transport mechanisms involved and assist in quantifying the effect of varied pneumatic permeability on pressure propagation.Laboratory work is underway at BYU to more carefully isolate the mechanisms of diffusive transport and pressure fluctuation in unsaturated conditions. A sealed soil column has been packed with sand and instrumented with a contaminant reservoir at one end and concentration sensor at the other. A mechanical syringe is used to vary the pressure within the tube, and pressure sensors have been emplaced.An affiliation has been established with researchers at the DOE Sandia laboratory to utilize a novel non-invasive vapor detector in our sealed-column laboratory work.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.