Kinetics of oxidation of selenite to selenate in the presence of oxygen, titania and light
No abstract available.
Geology topics
Publications and source records attributed to James O. Leckie.
No abstract available.
Laboratory experiments were conducted with well-characterized minerals to test the applicability of selective extraction schemes for Se and As partitioning in soils and sediments. Two specific steps were tested: the reductive dissolution of amorphous iron oxides and the oxidation of organic material. Selenium and As associated with amorphous iron oxides were usually not found in solution after reductive dissolution, due to readsorption onto other minerals unaffected by the extractant. Oxidants intended to dissolve organic material also oxidized Se(IV) adsorbed on a mineral to Se(VI), causing the release of Se(VI) to the extractant solution.
Laboratory adsorption experiments performed at environmentally significant lead (Pb) and cell concentrations indicate that the marine bacteria examined have significant binding capacities for Pb. However, the behavior governing Pb sorption onto gram-negative bacteria in seawater may be quite complex. The sorption kinetics appear to involve two distinct phases, i.e., a rapid removal of Pb from solution within the first few minutes, followed by a slow but nearly constant removal over many hours. Also, the average binding coefficient, calculated for Pb sorption onto bacteria and a measure of binding intensity, increases with decreasing sorption density (amounts of bacteria-associated Pb per unit bacterial surface) at low cell concentrations (10 5 cells ml −1 ), but decreases with decreasing sorption density at higher cell concentrations (10 7 cells ml −1 ). The latter effect is apparently due to the production of significant amounts of extra-cellular organics at high cell concentrations that compete directly with bacterial surfaces for available lead. Lead toxicity and active uptake by marine bacteria did not appear significant at the Pb concentrations used.