Mobilization and transport of organic compounds from reservoir rock and caprock in geological carbon sequestration sites

Supercritical CO₂ (scCO₂) is a good solvent for organic compounds such as benzene, toluene, ethyl-benzene, and xylene (BTEX), phenols, and polycyclic aromatic hydrocarbons (PAHs). Monitoring results from geological carbon sequestration (GCS) field tests have shown that organic compounds are mobilized following CO₂ injection. Such results have raised concerns regarding the potential for groundwater contamination by toxic organic compounds mobilized during GCS. Knowledge of the mobilization mechanism of organic compounds and their transport and fate in the subsurface is essential for assessing risks associated with GCS. Extraction tests using scCO₂ and methylene chloride (CH₂Cl₂) were conducted to study the mobilization of volatile organic compounds (VOCs, including BTEX), the PAH naphthalene, and n-alkanes by scCO₂ from representative reservoir rock and caprock obtained from depleted oil reservoirs and coal from an enhanced coal-bed methane recovery site. Results showed that the extent of mobilization for the organic compounds was a function of the source rock. In fate and transport sand column experiments, moisture content was found to have an important influence on the transport of the organic compounds. In dry sand columns the majority of the compounds were retained in the column except benzene and toluene. In wet sand columns the mobility of the BTEX was much higher than that of naphthalene. Based upon the results determined for the reservoir rock, caprock, and coal samples studied here, the risk to aquifers from contamination by organic compounds appears to be relatively low; however, further work is necessary to fully evaluate the risks.     

An Empirical Evaluation of the Influence of Ethanol on Natural Attenuation of Gasoline Constituents

Since the 1990s, questions have arisen as to whether the release of ethanol‐blended fuel will inhibit natural attenuation of other gasoline constituents in groundwater. This study evaluated the hypothesis that ethanol affects hydrocarbon attenuation and whether the use of ethanol‐blended fuel alters the applicability of monitored natural attenuation (MNA) as an approach for managing risks at fuel‐release sites. Groundwater data from California's GeoTracker database were used to compare attenuation of benzene, toluene, methyl tert‐butyl ether (MTBE), and tert‐butyl alcohol (TBA) at sites with and without detections of ethanol. Excel‐based tools were developed to conduct attenuation evaluations on thousands of wells simultaneously. Ethanol was detected at least once in 4.5% of the wells and 0.6% of the samples of which it was analyzed. The distribution of Mann‐Kendall concentration trend analysis results and first‐order attenuation rates were essentially the same at sites with or without ethanol detections. Median plume lengths were shorter at sites where ethanol had not been detected compared to sites where ethanol was detected (36 vs. 43 m for benzene; 36 vs. 42 m for toluene; 43 vs. 52 m for MTBE; and 44 vs. 59 m for TBA). However, the distribution of plume lengths was similar irrespective of ethanol concentrations, suggesting other factors may influence plume elongation. Finally, while anaerobic ethanol degradation can result in methane generation, the distributions of methane concentrations were the same at sites with and without ethanol detections. These results suggest that the use of ethanol‐blended fuel should not limit the application of MNA at most biodegrading fuel‐release sites.     

Analysis of Urban Atmosphere Plume Concentration Fluctuations

Concentration variability in the fast-response tracer dataset for continuous, near-surface, point source releases in the urban core from the Joint Urban 2003 field study is analyzed. Concentration variability for conditionally and unconditionally sampled time series is characterized by probability densities, concentration fluctuation intensity, skewness, and kurtosis. Significant day-night differences in plume dispersion are observed. Relative to daytime, nighttime plumes were more likely to have reduced concentration fluctuation intensities, higher normalized surface concentrations, suppressed vertical mixing, and a greater prevalence of Gaussian-like distributions rather than log-normal or mixed mode distributions. This was in spite of the similar stability and turbulence conditions in the urban core for day and night. The potential roles of flow meander and thermal stability in explaining these differences are examined. Probability densities of concentration are found to be a strong function of fluctuation intensity. There are few differences in probability densities between day and night when classified by fluctuation intensity. There are no appreciable differences between conditional and unconditional probability densities and only small differences between conditional and unconditional sampling statistics relative to the larger differences usually observed in more homogeneous settings. Fluctuation intensity, skewness, and kurtosis are higher for the daytime experiments, and closer to the source, but show little difference between conditional and unconditional results over most of their range of values. The log-normal distribution provides a better overall fit to a broader range of the dataset than the exponential or clipped-normal distributions.     

Satellite motion in a Manev potential with drag

In this paper, we consider a satellite orbiting in a Manev gravitational potential under the influence of an atmospheric drag force that varies with the square of velocity. Using an exponential atmosphere that varies with the orbital altitude of the satellite, we examine a circular orbit scenario. In particular, we derive expressions for the change in satellite radial distance as a function of the drag force parameters and obtain numerical results. The Manev potential is an alternative to the Newtonian potential that has a wide variety of applications, in astronomy, astrophysics, space dynamics, classical physics, mechanics, and even atomic physics.     

Temporal Trends of Dissolved Trace Metals in Jamaica Bay,NY: Importance of Wastewater Input and Submarine Groundwater Discharge in an Urban Estuary

Jamaica Bay, NY, is a highly urbanized estuary within the boroughs of New York City conspicuously lacking published information on dissolved trace metal concentrations. The current study examines the distribution and cycling of trace metals in that embayment with data gathered during cruises in November 2004, April 2005, and June 2006. Most of the metal distributions (Fe, Zn, Co, Ag, Cu, Pb, Ni) in the water column are explained by the input of substantial volumes of treated wastewater effluent. However, several lines of evidence suggest that submarine groundwater discharge (SGD) is also an important source of dissolved Fe, Zn, Co, Ni, and isotopically distinct stable Pb ratios (²⁰⁶Pb, ²⁰⁷Pb, ²⁰⁸Pb) in the Bay. Conversely, the recirculated seawater component of SGD is an apparent sink for dissolved Mo. This study provides the first measurements of dissolved trace metals in the Jamaica Bay water column and subterranean estuary and provides evidence for trace metal input due to SGD.