Publications

The rate of Cd2+ sorption by a calcareous aquifer sand was characterized by two reaction steps, with the first step reaching completion in 24 hours. The second step proceeded at a slow and nearly constant rate for at least seven days. The first step includes a fast adsorption reaction which is followed by diffusive transport into either a disordered surface film of hydrated calcium carbonate or in

The rate of Cd2+ sorption by calcite was determined as a function of pH and Mg2+ in aqueous solutions saturated with respect to calcite but undersaturated with respect to CdCO3. The sorption is characterized by two reaction steps, with the first reaching completion within 24 hours. The second step proceeded at a slow and nearly constant rate for at least 7 days. The rate of calcite recrystallizati

Infiltration of wastes containing creosote and pentachlorophenol from surface impoundments at an abandoned wood-treatment facility near Pensacola, Florida, resulted in contamination of the underlying sand and gravel aquifer. Pond sludges and sediments near the source were contaminated with 2- to 5-ring azaarenes having log Kow values of from 2.0 to 5.6. However, the ground water contained only aza

A method has been developed to establish steady state flow of water in an unsaturated soil sample spinning in a centrifuge. Theoretical analysis predicts moisture conditions in the sample that depend strongly on soil type and certain operating parameters. For Oakley sand, measurements of flux, water content, and matric potential during and after centrifugation verify that steady state flow can be

A spectrometric technique utilizing electrothermal vaporization (graphite furnace) and gas phase-multiple wavelength absorption with photodiode array detection is used to characterize crude oil.

e have previously shown that primary productivity in San Francisco Bay, USA, is highly correlated with phytoplankton biomass B (chlorophyll a concentration) and an index of light avallability in the photic zone, 2, I, (photic depth times surface irradiance). To test the generality of this relation, we compiled data from San Francisco Bay and 5 other USA estuarine systems (Neuse and South Rivers, P

A mathematical model is developed to describe the fate of hydrocarbon constituents of petroleum products introduced to soils as an immiscible liquid from sources such as leaking underground storage tanks and ruptured pipelines. The problem is one of multiphase transport (oil (immiscible), air, and water phases) of a reactive contaminant with constituents such as benzene, toluene, and xylene found

Playa-lake basins of the Southern High Plains, Texas and New Mexico, may originate wherever water periodically can collect in a surficial depression. They expand, however, by hydrologic and geomorphic processes including (1) dissolution of lithologic carbonates by infiltrating water; (2) transport downward of fine-grained clastic and organic material by the infiltrating ground water, leading to co

No abstract available.

In this paper we develop a numerical solution to equations developed in part 1 (M. Y. Corapcioglu and A. L. Baehr, this issue) to predict the fate of an immiscible organic contaminant such as gasoline in the unsaturated zone subsequent to plume establishment. This solution, obtained by using a finite difference scheme and a method of forward projection to evaluate nonlinear coefficients, provides

Methodologies that account for specific types of chemical reactions in the simulation of solute transport can be developed so they are compatible with solution algorithms employed in existing transport codes. This enables the simulation of reactive transport in complex multidimensional flow regimes, and provides a means for existing codes to account for some of the fundamental chemical processes t

Dissolution of synthetic strontianite-aragonite solid solutions was followed analytically to stoichiometric saturation using large solid to solution ratios in CO2-H2O solution at 25 and 76°C. The compositional dependence of the equilibrium constant was calculated from the composition of saturated (stoichiometric) solutions and used to calculate the activities and activity coefficients of CaCO3 and