Performance of Full‐Scale Enhanced Reductive Dechlorination in Clay Till

At a low permeability clay till site contaminated with chlorinated ethenes (Gl. Kongevej, Denmark), enhanced reductive dechlorination (ERD) was applied by direct push injection of molasses and dechlorinating bacteria. The performance was investigated by long‐term groundwater monitoring, and after 4 years of remediation, the development of degradation in the clay till matrix was investigated by high‐resolution subsampling of intact cores. The formation of degradation products, the presence of specific degraders Dehalococcoides spp. with the vinyl chloride (VC) reductase gene vcrA, and the isotope fractionation of trichloroethene, cis‐dichloroethene (cis‐DCE), and VC showed that degradation of chlorinated ethenes occurred in the clay till matrix as well as in sand lenses, sand stringers, and fractures. Bioactive sections of up to 1.8 m had developed in the clay till matrix, but sections, where degradation was restricted to narrow zones around sand lenses and stringers, were also observed. After 4 years of remediation, an average mass reduction of 24% was estimated. Comparison of the results with model simulation scenarios indicate that a mass reduction of 85% can be obtained within approximately 50 years without further increase in the narrow reaction zones if no donor limitations occur at the site. Long‐term monitoring of the concentration of chlorinated ethenes in the underlying chalk aquifer revealed that the aquifer was affected by the more mobile degradation products cis‐DCE and VC generated during the remediation by ERD.     

A Least-squares Window Curves Method for Interpretation of Magnetic Anomalies Caused by Dipping Dikes

We have developed a least-squares method to determine simultaneously the depth and the width of a buried thick dipping dike from residualized magnetic data using filters of successive window lengths. The method involves using a relationship between the depth and the half-width of the source and a combination of windowed observations. The relationship represents a family of curves (window curves). For a fixed window length, the depth is determined for each half-width value by solving one nonlinear equation of the form f (z) = 0 using the least-squares method. The computed depths are plotted against the width values representing a continuous curve. The solution for the depth and the width of the buried dike is read at the common intersection of the window curves. The method involves using a dike model convolved with the same moving average filter as applied to the observed data. As a result, this method can be applied to residuals as well as to measured magnetic data. Procedures are also formulated to estimate the amplitude coefficient and the index parameter. The method is applied to theoretical data with and without random errors. The validity of the method is tested on airborne magnetic data from Canada and on a vertical component magnetic anomaly from Turkey. In all cases examined, the model parameters obtained are in good agreement with the actual ones and with those given in the published literature.     

Identifying critical combination of roadside slopes susceptible to rainfall-induced failures

Natural Hazards - The stability of roadside slopes is vital for the smooth operation of the highway transportation system. The failure of slopes adjacent to the highway corridors disrupts the...     

Natural manganese oxide: Combined analytical approach for solid characterization and arsenic retention

To understand the retention of As on a natural manganese sand, the structural, textural and chemical properties of the solid were first investigated by combining scanning electron microscopy (SEM), transmission electron microscopy (TEM), electron-energy-loss spectroscopy (EELS), X-ray diffraction (XRD), BET N₂ gas adsorption, diffuse reflectance Fourier transform infrared (FT-IR) spectroscopy and X-ray photoelectron spectroscopy (XPS) analysis. Manganese sand could be mainly described as a mixture of a phyllomanganate, lithiophorite [(Al,Li)MnO₂(OH)₂], and pyrolusite (MnO₂). Iron particle, kaolinite and gibbsite type-phases were also observed. Particles organization led to the presence of a mesoporosity with pore diameters ranging from 100 to 200 Å and a specific surface area of 23 m² g⁻¹. Contact with an As(V) solution (0.67 mmol L⁻¹) led to an average fractional surface coverage of 0.4. Both As (V) and (III) were present on the surface of the sand in a 1:1 ratio. As(V) was sorbed on lithiophorite-type particles through surface complexation type reaction. As(III) was thought to result from As(V) reduction mechanism on iron particles.     

Feasibility of geoelectrical monitoring and multiphase modeling for process understanding of gaseous CO2 injection into a shallow aquifer

Potential pathways in the subsurface may allow upwardly migrating gaseous CO₂ from deep geological storage formations to be released into near surface aquifers. Consequently, the availability of adequate methods for monitoring potential CO₂ releases in both deep geological formations and the shallow subsurface is a prerequisite for the deployment of Carbon Capture and Storage technology. Geoelectrical surveys are carried out for monitoring a small-scale and temporally limited CO₂ injection experiment in a pristine shallow aquifer system. Additionally, the feasibility of multiphase modeling was tested in order to describe both complex non-linear multiphase flow processes and the electrical behavior of partially saturated heterogeneous porous media. The suitability of geoelectrical methods for monitoring injected CO₂ and geochemically altered groundwater was proven. At the test site, geoelectrical measurements reveal significant variations in electrical conductivity in the order of 15?C30?%. However, site-specific conditions (e.g., geological settings, groundwater composition) significantly influence variations in subsurface electrical conductivity and consequently, the feasibility of geoelectrical monitoring. The monitoring results provided initial information concerning gaseous CO₂ migration and accumulation processes. Geoelectrical monitoring, in combination with multiphase modeling, was identified as a useful tool for understanding gas phase migration and mass transfer processes that occur due to CO₂ intrusions in shallow aquifer systems.     

Dissolution mechanisms of goethite in the presence of siderophores and organic acids

In dynamic natural systems such as soils and surface waters, transient biogeochemical processes can induce strong chemical non-steady-state conditions. In this paper, we investigate the effects of non-steady-state conditions on ligand-controlled iron oxide dissolution. The rates of goethite dissolution at pH 6 in the presence of low molecular weight organic acids (oxalate, citrate or malonate) were observed. Non-steady-state conditions were induced by rapid additions of fungal, bacterial or plant siderophores. In the presence of the low molecular weight organic acids, dissolved iron concentrations are below detection limit as predicted by equilibrium solubility calculations. The rapid addition of the siderophores triggered reproducible, fast dissolution of kinetically labile iron from the iron oxide surface. The same effect was observed upon rapid additions of high citrate concentrations to goethite-oxalate suspensions. The concentration of the labile iron pool at the mineral surface was a function of the surface concentration of the low molecular weight organic acids and of the reaction time before addition of the siderophores. Isotopic exchange with ⁵⁹Fe independently confirmed the existence of the labile iron pool before addition of the siderophore. A dissolution mechanism was elucidated that is consistent with these observations and with accepted models of ligand-controlled dissolution. We conclude that the fast dissolution reaction observed here is an important process in biological iron acquisition and that it is based on a general geochemical mechanism.