What factors determine trace metal contamination in Lake Tonga (Algeria)?

A study of trace metal (TM) contamination was conducted at Lake Tonga (Algeria), a site surrounded by several indirect contamination point sources such as an abandoned mine and steelworks. Studying two sampling sites over four seasons, we were able to depict the spatial and temporal variability of TM contamination in the lake. Among the seven TM examined (Pb, Cd, Fe, Zn, Ni, Cu, and Cr), only Fe, Pb, and Cd showed concentrations significantly higher than the site’s geological background. The contamination index (sediment concentration/background concentration) calculated for these three TM (Cd = 1.9?±?1.6, Fe = 6.8?±?1.8, and Pb = 3.3?±?2.6) clearly indicated anthropogenic contamination. Sediment TM contamination differed both between sampling sites and seasons despite environmental variables (e.g., oxygen and pH) being similar, thus suggesting different TM contamination sources. Fe contamination was high at the two sampling sites and over all studied seasons, possibly indicating general lake-scale Fe contamination, probably related to atmospheric deposition of steelworks emissions both on the lake and within the watershed. Lake tributaries were further suspected of channeling Fe contamination from the watershed into the lake. On the other hand, the sampling site close to the outlet was especially rich in Cd and Pb typically reflecting contamination by mine wastes. The indirect connection between the abandoned mine and the lake indicates that runoff of mine leachates through groundwater was likely a candidate in explaining the specificity of the TM contamination in this part of the lake. This study provides insights for management of TM contamination by addressing both spatial and temporal variability within the lake as well as differences in contamination sources.     

Photochemical Degradation of Aqueous Polyvinyl Alcohol in a Continuous UV/H<Subscript>2</Subscript>O<Subscript>2</Subscript> Process: Experimental and Statistical Analysis

Polyvinyl alcohol (PVA), being a dominant contributor of total organic carbon (TOC) in textile wastewater, is not easily degradable by conventional methods of wastewater treatment. This study investigates the degradation of aqueous PVA in a continuous UV/H₂O₂ photoreactor since the feeding strategy of hydrogen peroxide proves to have considerable effects on the process performance. Response surface methodology involving the Box–Behnken method is adopted for the experimental design to study the effects of operating parameters on the process performance. Experimental analysis shows that the TOC removal varies from 16.11 to 42.70 % along with a reduction of the PVA molecular weights from 56.7 to 95.3 %. The TOC removal is significantly lower than the molecular weight reduction due to the generation of the intermediate products during oxidation. Operating the UV/H₂O₂ process in a continuous mode facilitates the degradation of highly concentrated polymeric solutions using a relatively small hydrogen peroxide concentration in the feed with a small residence time ranges from 6.13 to 18.4 min.     

Identification and Model Predictive Control (MPC) of Aqueous Polyvinyl Alcohol Degradation in UV/H2O2 Photochemical Reactors

Journal of Polymers and the Environment - The performance of two continuous UV/H2O2 photoreactors in series under unsteady-state condition is studied. An input–output dynamic model is...     

Dynamics of harmful dinoflagellates driven by temperature and salinity in a northeastern Mediterranean lagoon

To attempt to determine the effects of temperature and salinity on the dynamics of the dinoflagellate community, a monthly sampling was carried out from October 2008 to March 2009 at eight sampling stations in Ghar El Melh Lagoon (GML; Mediterranean Sea, Northern Tunisia). Dinoflagellates were dominant among plankton, accounting for 73.9 % of the lagoon’s overall plankton community, and were comprised of 25 different species among which 17 were reported in the literature as harmful. While no significant difference was found in the distribution of dinoflagellates among the stations, a strong monthly difference was observed. This temporal variability was due to an increase in the abundance of Prorocentrum micans from December to February, leading to a strong decrease in the Shannon diversity index from station to station. At the onset of P. micans development, dinoflagellate abundances reached 1.26.10⁵ cells l^?1. A redundance analysis indicates that both temperature and salinity have a significant effect on the dynamics of the dinoflagellate community. Using a generalized additive model, both temperature and salinity appear to have significant nonlinear relationships with P. micans abundances. Model predictions indicate that outbreaks of P. micans may occur at a temperature below 22.5 °C and with salinity above 32.5. We discuss our results against a backdrop of climate change which, by affecting temperature and salinity, is likely to have an antagonistic impact on P. micans development and subsequently on the dinoflagellate dynamics in GML.     

Assessment of nitrogen and phosphate balance and the roles of bacteria and viruses at the water-sediment interface in the Allal El Fassi reservoir (Morocco)

Balances of nitrogen and phosphate were studied in the Allal El Fassi reservoir (Morocco); the results showing that nitrogen input (296 mg m^?2 d^?1) was 161 % higher than output (183 mg m^?2 d^?1). Phosphate input (35.65 mg m^?2 d^?1) was 865 % higher than output (4.12 mg m^?2 d^?1), causing a progressive increase in the internal phosphate stock. Sedimentation flux was equally high (53.80 and 18 mg m^?2 d^?1) for both nitrogen and phosphate input, mainly from the Sebou River and in particulate form which immediately settles upon arrival in the reservoir. The release of nitrogen and phosphate from the sediment (5.40 and 1.15 mg m^?2 d^?1, respectively) depended on physicochemical and biological (bacteria and viruses) variability and the calcareous nature of the catchment basin. Calcium-bound phosphate prevailed in the reservoir. Drastic control of phosphate input is suggested to avoid accumulation of calcium-bound phosphate which may dissociate and thereby contribute to eutrophication.     

Photochemical Kinetic Modeling of Degradation of Aqueous Polyvinyl Alcohol in a UV/H<Subscript>2</Subscript>O<Subscript>2</Subscript> Photoreactor

This study presents a photochemical kinetics model to describe the degradation of water-soluble PVA (Polyvinyl Alcohol) polymer in a UV/H₂O₂ batch reactor. Under the effect of UV light, the photolysis of hydrogen peroxide into hydroxyl radicals can generate a series of polymer scission reactions. For a better understanding and analysis of the UV/H₂O₂ process in the cracking of the PVA macromolecules, a chemical reaction mechanism of the degradation process and a relevant photochemical kinetics model are developed to describe the disintegration of the polymer chains. Taking into account the probabilistic fragmentation of the polymer, the statistical moment approach is used to model the molar population balance of live and dead polymer chains. The model predicts the PVA molecular weight reduction, the acidity of the solution, and hydrogen peroxide residual. In addition to previously published data collected in this laboratory, a new set of experiments were conducted using a 500 mg/L PVA aqueous for different hydrogen peroxide/PVA ratios for model validation. Measurements of average molecular weights of the polymer, hydrogen peroxide concentrations and pH of the PVA solution were determinant factors in constructing a reliable photochemical model of the UV/H₂O₂ process. Experimental data showed a decrease in the PVA molecular weight and a buildup of the solution acidity. The experimental data also served to determine the kinetics rate constants of the PVA photochemical degradation and validate the model whose predictions are in good agreement with data. The model can provide a comprehensive understanding of the impact of the design and operational variables.