Geophysical Assessment of a Proposed Landfill Site in Fredericktown, Missouri.

In cooperation with the U.S. Environmental Protection Agency (EPA), the U.

Thioarsenite Detection and Implications for Arsenic Transport in Groundwater.

Arsenic toxicity and mobility in groundwater depend on its aqueous speciation. Uncertainty about the methods used for measuring arsenic speciation in sulfate-reducing environments hampers transport and fate analyses and the development of in situ remediation approaches for treating impacted aquifers. New anion-exchange chromatography methods linked to inductively coupled plasma mass spectrometry (ICP-MS) are presented that allow for sample/eluent pH matching.

Evaluating relationships between total dissolved solids (TDS) and total suspended solids (TSS) in a mining-influenced watershed.

Measurement of total suspended solids (TSS) and total dissolved solids (TDS) loadings in streams is often used to assess potential impacts from mining on surface water quality within a drainage basin. It has been suggested that TSS could be used as an indicator to estimate TDS loading through the use of a TDS/TSS ratio. The reliability of this approach was tested by examining empirical linear relationships between TSS and TDS loads at three locations within a mining-influenced watershed in Colorado.

Examining the efficiency of muffle furnace-induced alkaline hydrolysis in determining the titanium content of environmental samples containing engineered titanium dioxide particles.

A novel muffle furnace (MF)-based potassium hydroxide (KOH) fusion digestion technique was developed and evaluated for different titanium dioxide materials in various solid matrices. Digestion of different environmental samples containing sediments, clay minerals and humic acid with and without TiO(2) particles was first performed utilizing the MF-based KOH fusion technique and its dissolution efficacy was compared to a Bunsen burner (BB)-based KOH fusion method. The three types of TiO(2) particles (anatase, brookite and rutile) were then digested with the KOH fusion techniques and microwave (MW)-based nitric (HNO3)–hydrofluoric (HF) mixed acid digestion methods.

Delineating landfill leachate discharge to an arsenic contaminated waterway.

Discharge of contaminated ground water may serve as a primary and on-going source of contamination to surface water. A field investigation was conducted at a Superfund site in Massachusetts, USA to define the locus of contaminant flux and support source identification for arsenic contamination in a pond abutting a closed landfill. Subsurface hydrology and ground-water chemistry were evaluated in the aquifer between the landfill and the pond during the period 2005-2009 employing a network of wells to delineate the spatial and temporal variability in subsurface conditions.

Nest construction by a ground-nesting bird represents a potential trade-off between egg crypticity and thermoregulation.

Predation selects against conspicuous colors in bird eggs and nests, while thermoregulatory constraints select for nest-building behavior that regulates incubation temperatures. We present results that suggest a trade-off between nest crypticity and thermoregulation of eggs based on selection of nest materials by piping plovers (Charadrius melodus), a ground-nesting bird that constructs simple, pebble-lined nests highly vulnerable to predators and exposed to temperature extremes. Piping plovers selected pebbles that were whiter and appeared closer in color to eggs than randomly available pebbles, suggesting a crypsis function.

Examination of arsenic speciation in sulfidic solutions using X-ray absorption spectroscopy.

Both thioarsenites and thioarsenates have been demonstrated to exist in sulfidic waters, yet there is uncertainty regarding the geochemical conditions that govern the formation of these arsenic species. The purpose of this research was to use advanced spectroscopy techniques, speciation modeling, and chromatography to elucidate the chemical speciation of arsenic in sulfidic solutions initially containing arsenite and sulfide. Results of X-ray absorption spectroscopy (XAS) show that experimental solutions contained mixtures of arsenite and thioarsenites with increasing substitution of sulfur for oxygen on arsenic as the sulfide concentration increased.

Chromium-removal processes during groundwater remediation by a zerovalent iron permeable reactive barrier.

Solid-phase associations of chromium were examined in core materials collected from a full-scale, zerovalent iron permeable reactive barrier (PRB) at the U.S. Coast Guard Support Center located near Elizabeth City, NC.

Use of synthetic zeolites for arsenate removal from pollutant water.

Arsenic is known to be a hazardous contaminant in drinking water that causes arsenical dermatitis and skin cancer. In the present work, the potential use of a variety of synthetic zeolites for removal of arsenic from water below the current and proposed EPA MCL has been examined at room temperature. Experiments have been conducted to examine the extent of arsenic removal as a function of pH.

Nonbiological removal of cis-dichloroethylene and 1,1-dichloroethylene in aquifer sediment containing magnetite.

The U.S. EPA Technical Protocol for Evaluating Natural Attenuation of Chlorinated Solvents in Groundwater emphasizes biological reductive dechlorination as the primary mechanism for destruction of chlorinated solvents.

Kinetics and mechanisms of Zn complexation on metal oxides using EXAFS spectroscopy.

Zn(II) sorption onto Al and Si oxides was studied as a function of pH (5.1-7.52), sorption density, and ionic strength.

Speciation of arsenic in sulfidic waters.

Formation constants for thioarsenite species have been determined in dilute solutions at 25°C, ΣHS from 10 to 10 M, ΣAs from 10 to 10 M, and pH 7 and 10. The principal inorganic arsenic species in anoxic aquatic systems are arsenite, As(OH) , and a mononuclear thioarsenite with an S/As ratio of 3:1. Thioarsenic species with S/As ratios of 1 : 1,2 : 1, and 4 : 1 are lesser components in sulfidic solutions that might be encountered in natural aquatic environments.

Use of hydrochloric acid for determinining solid-phase arsenic partitioning in sulfidic sediments.

We examined the use of room-temperature hydrochloric acid (1-6 M) and salt solutions of magnesium chloride, sodium carbonate, and sodium sulfide for the removal of arsenic from synthetic iron monosulfides and contaminated sediments containing acid-volatile sulfides (AVS). Results indicate that acid-soluble arsenic reacts with H2S released from AVS phases and precipitates at low pH as disordered orpiment or alacranite. Arsenic sulfide precipitation is consistent with geochemical modeling in that conditions during acid extraction are predicted to be oversaturated with respect to orpiment, realgar, or both.

Rates of hydrous ferric oxide crystallization and the influence on coprecipitated arsenate.

Arsenate coprecipitated with hydrous ferric oxide (HFO) was stabilized against dissolution during transformation of HFO to more crystalline iron (hydr)oxides. The rate of arsenate stabilization approximately coincided with the rate of HFO transformation at pH 6 and 40 degrees C. Comparison of extraction data and X-ray diffraction results confirmed that hematite and goethite were the primary transformation products.