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  • Salomonsen McElroy posted an update 3 months, 1 week ago

    The present study investigates the efficiency of a three-dimensional electro-peroxone (3D/E-peroxone) reactor filled with TiO2-GAC in removing diuron from aqueous solution and in the remediation of real pesticide wastewater. The behavior of the system in terms of the effect of independent variables on diuron was investigated and optimized by RSM-CCD and ANN-GA methods. Both approaches proved to have a very good performance in the modeling of the process and determined the optimum condition of the independent variables as follows initial pH = 10, applied current = 500 mA, supporting electrolyte = 0.07 M, ozone concentration = 10 mg L-1, and reaction time = 10 min. The 3D/E-peroxone process achieved a synergistic effect in diuron abatement and reduced significantly energy consumption, as compared to its individual components. H2O2 concentration generated in the electrolysis system was notably increased in the presence of TiO2-GAC microparticles. The BOD5/COD ratio of the real pesticide wastewater increased from 0.049 to 0.571 within 90 min treatment. Giving to the considerable enhancement of the biodegradability of the wastewater, this study strongly suggests that the 3D/E-peroxone process can be considered as a promising pretreatment step before a biological treatment process to produce intermediates which are more easily degradable by microorganisms.We report the photoelectrochemical application of a visible light active FTO-Cu2O/Ag3PO4 photoanode for the abatement of sulfamethoxazole in water. The as-synthesised photoanodes were characterised using XRD, field emission SEM, EDX, diffuse reflectance UV-vis, impedance spectroscopy and chronoamperometry. The results obtained confirmed a successful formation of p-n heterojunction at the Cu2O/Ag3PO4 interface. The highest photocurrent response of 0.62 mAcm-2 was obtained for the composite photoanode which was four times higher than pure Cu2O and about three times higher than pristine Ag3PO4. The photoanode gave 67% removal efficiency within 2 h upon its photoelectrochemical application in the degradation of sulfamethoxazole with 1.5 V bias potential at pH 6.2. The FTO-Cu2O/Ag3PO4 electrode was also applied in the treatment of a cocktail of synthetic organics containing sulfamethoxazole and orange II dye. The photogenerated holes was found to be the major oxidant and the photoanodes was stable and reusable.In this paper, the influence of several aquatic factors (the nature of catalyst, the initial pH and the initial concentration of the pollutant) on the photocatalytic degradation of diclofenac (DFC), one of the most widely prescribed anti-inflammatory non-steroidal drug, was studied. Also, in order to examine the intensification process, the variation of the photocatalytic DFC degradation in the presence of sodium persulfate (PPS) was analyzed. It was found that, compared to titanium dioxide (TiO2), the zinc oxide (ZnO) photocatalyst performed exceptionally well, with a 96.13% DFC degradation efficiency after 150 min. The photodegradation of DFC by ZnO catalyst fitted well the Langmuir-Hinshelwood kinetic model. The maximum efficiency is 97.27% for simulated solar-UVA/ZnO/PPS and 77% for simulated solar-UVA/ZnO. In order to determine the optimal conditions leading to the maximization of DFC removal, an artificial neural network (ANN) modeling approach combined with genetic algorithm (GA) was applied. selleckchem The best ANN determined had a correlation of 0.999 and it was further used in the process optimization where a 99.7% degradation efficiency was identified as the optimum under the following conditions DFC initial concentration 37,9 mg L-1, pH 5,88 and PPS initial concentration 500 mg L-1. The effectiveness of the process and the toxicity of the pharmaceutical pollutants and their by-products were also evaluated and confirmed by the biological tests using liver and kidney of Mus musculus mice.Contamination levels and temporal trends of polybrominated diphenyl ethers (PBDEs) and some alternative brominated flame retardants (BFRs) were examined in a dated sediment core from the deepest part of the Beppu Bay, southwestern Japan. PBDEs were found in the upper layers of 0-15 cm depth at concentrations ranging from 5200 to 32,600 pg g-1 with the peak estimated at 1995. Decabromodiphenyl ether (BDE-209) was the most abundant congener, accounting for 96% in average of total PBDEs. The vertical profile of BDE-209 observed in our sediment core generally agreed with the historical pattern of domestic demand of commercial deca-BDE mixtures in Japan, and perfectly matched with maximum stock of these products (i.e., 42,000 tons in 1995). Among alternative BFRs, only decabromodiphenyl ethane (DBDPE), a replacement of deca-BDE, was found at significant levels with concentrations of 69-850 pg g-1 in sediment layers dated between 1991 and 2011. Ratios of DBDPE to BDE-209 gradually increased during this period, implying opposite trends of these two compounds and the role of DBDPE as a deca-BDE’s alternative. The occurrence of deca-BDE components in sediments may pose medium risk to benthic aquatic life, while the ecological risk of other PBDE homologs and DBDPE was negligible.Knowledge about bioaccumulation and trophic transfer in food webs is of tremendous importance in contaminant hazards evaluation. Perfluoroalkyl acids (PFAAs) are widely distributed, and its emissions to coastal areas have posed a threat to the health of marine organisms and consumers. In this study, 15 species were sampled from Qinzhou Bay of the South China Sea. The concentrations of PFAAs in organisms were detected by liquid chromatography-mass spectrometry, and the trophic positions of organisms were constructed based on nitrogen isotope analysis. PFAAs were found in all organisms. The contents of PFOS in all organisms were higher than of PFOA, and the proportions of short-chain PFAAs were higher in the low trophic positioned organisms, while long-chain PFAAs were higher in the high trophic positioned organisms. Moreover, the bioaccumulation factors (BAFs) increased with the increasing number of fluorocarbon atoms. The trophic magnification factor (TMF) and the biomagnification factors (BMFs), calculated from the constructed food webs, together suggested potential biomagnification effects of PFOS, while less clear results were found for PFOA.

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