Evaluation of methylene blue and riboflavin for the photosensitized degradation of ethylene glycol

Degradation rates ranging from 0.22 ± 0.11 to 1.52 ± 0.50 mg/L-h were measured for ethylene glycol in riboflavin solutions exposed to natural sunlight. Significant degradation rates were noted in systems using 6 and 10 mg/L riboflavin at pH values of 4, 7, and 10. No significant degradation was found in systems using methylene blue as the photosensitizing agent. Possible mechanisms for ethylene glycol degradation include a combination hydrogen or electron abstraction by an excited photosensitizer and reaction with singlet oxygen or reaction with superoxide radicals.     

Industrial pollution discharges from the West African region

Information on the type and quantity of industrial pollutants from major land-based sources entering the marine environment through direct coastal discharges or indirectly through rivers, as well as on the present status of industrial waste management (treatment and disposal) practices, are provided for the West African region. Most of the data utilized in this analysis were collected by six UNIDO experts who visited the eighteen countries of the West African region during the period of January through August 1980. Industrial operations were visited and information was collected from the various ministries involved with industrial development and environmental protection. Estimates of the mass of pollutants discharged to the ocean were based upon production rates used in conjunction with actual measurements made by the industries located in the countries visited; studies reported in the literature; and an extrapolation of the U.S. Environmental Protection Agency Effluent Standards for various industrial sectors. The West African region was divided into five zones closely approximating the major currents of the Atlantic Ocean. The estimated pollution discharged by the industrial sector was calculated for each of the zones by adding the contribution from each country assigned to a zone.     

Atypical plant–herbivore association of algal food and a kleptoplastic sea slug (Elysia clarki) revealed by DNA barcoding and field surveys

The identity of food sources and feeding preferences of specialist herbivores have been commonly inferred from spatial associations between consumer and food items. However, such basic information for well-known marine herbivores, sacoglossans (sea slugs), and their algal diets remains disappointingly lacking, especially from field studies. The sacoglossan, Elysia clarki (Pierce et al. in Molluscan Res 26:23–38, 2006), is kleptoplastic and sequesters chloroplasts from algal food to photosynthesize, so DNA identification of sequestered chloroplasts was employed to verify the algal species fed upon by the slug across its geographic range. The molecular information on the algae consumed by E. clarki was combined with field surveys of slugs and algae in slug habitats in the Florida Keys in July and August of 2008 in order to evaluate whether the diet of this herbivore could be predicted based on its spatial association with algae in the field. A considerable mismatch between food availability and kleptoplast identity was recorded. E. clarki commonly occupied areas devoid of potential food and often contained symbiotic plastids from algal species different from those most frequently found in the surveyed habitats. In three of the four study sites, algal species present were poor predictors of slug diet. These findings suggest that the photosynthetic capability of E. clarki may release the slug from the constraint of requiring proximity to its food sources and may allow for the potential lack of spatial coupling between this herbivore and its algal food. This combination of field surveys and DNA barcoding provided critical and previously unavailable information on herbivore feeding in this marine system.     

Lime stabilization and land disposal of cold region wastewater lagoon sludge

Effects of lime [Ca(OH)₂] stabilization upon the pathogenic population in accumulated solids associated with the operation of two aerated wastewater lagoons in Alaska and two facultative wastewater lagoons in northern Utah were evaluated. The subsequent drying, at a temperature of 12 °C, of the lime stabilized sludges on sand and soil beds was also investigated. The lime stabilization of the lagoon sludges was evaluated by dosing the sludges with lime and applying sludges to bench scale drying beds. Lime addition produced high fecal coliform reduction, and the limed sludges readily dewatered on both sand and soil beds.     

Arsenic and fluoride removal from groundwater by reverse osmosis

The reverse osmosis process was evaluated for removal of naturally occurring arsenic and fluoride from groundwater. Arsenic removal was affected by the prevalent arsenic species present in the water. Arsenic concentrations were reduced by approximately 60%–90% from nearly 80 μg/L. Fluoride concentrations were reduced by approximately 60% from nearly 1.7 mg/L.     

Degradation of ethylene glycol using Fenton's reagent and UV

Oxidation of ethylene glycol in aqueous solutions was found to occur with the addition of Fenton's reagent with further conversion observed upon UV irradiation. The pH range studied was 2.5-9.0 with initial H2O2 concentrations ranging from 100 to 1000 mg/l. Application of this method to airport storm-water could potentially result in reduction of chemical oxygen demand by conversion of ethylene glycol to oxalic and formic acids. Although the amount of H2O2 added follows the amount of ethylene glycol degraded, smaller H2O2 doses were associated with increases in the ratio of ethylene glycol removed per unit H2O2 added indicating the potential of pulsed doses or constant H2O2 feed systems. Ethylene glycol removal was enhanced by exposure to UV light after treatment with Fenton's reagent, with rates dependent on initial H2O2 concentration. In addition to ethylene glycol, the principle products of this reaction, oxalic and formic acids, have been shown to be mineralized in other HO generating systems presenting the potential for ethylene glycol mineralization in this system with increased HO* production.