Chlorinated organics from chlorine used in water treatment

The contribution from impurities in chlorine to levels of chlorinated organics found in potable water after chlorination was investigated. Techniques for sampling of chlorine and gas chromatography (GC) determination of chlorinated organics in chlorine are described. The detection limits were better than 1 ppm for each of chloromethane, dichloromethane, chloroform, carbon tetrachloride, trichloroethylene, tetrachloroethylene, hexachloroethane, hexachloropropane and hexachlorobenzene in chlorine. With the exception of chloroform which occasionally accounted for nearly 1 μg l⁻¹ in water, the levels of the nine compounds in chlorine accounted for less than 0.1 μg l⁻¹ of each compound in chlorinated water from 10 Canadian treatment plants. The occurrence of these nine and 28 additional chlorinated organics previously detected in water supplies was determined by aid of liquid-liquid extraction of water samples. Seven compounds, including chloroform, carbon tetrachloride, trichloroethylene and tetrachloroethylene were detected, usually at levels ranging from 0.1 to 1 μg l⁻¹ in chlorinated water from the treatment plant.     

Evaluating a mass transfer model for the dissolution of organics from oil films into water

A mass-transfer model analogous to one used to describe the volatilization of organics from natural waters was used to describe the dissolution of constituent organics from a floating oil film into the underlying water. The mass flux of a material across the oil-water interface was depicted using an oil-phase mass-transfer coefficient, k_o a water-phase mass-transfer coefficient, k_w, a partition coefficient, P, describing the equilibrium partitioning of a substance between oil and water, and the concentrations of the substance in the oil and water, C_o and C_w, in the following expression: Rates of dissoltion were observed to vary with properties of the solute, P, the oil (viscosity, P, oil depth) and the environment (oil and water mixing, water depth). The observed rates of dissolution of chemicals from a low-viscosity oil (heptane) varied by a factor of 10⁴ between the most rapidly and most slowly dissolving materials.     

Fate of nine recycled water trace organic contaminants and metal(loid)s during managed aquifer recharge into a anaerobic aquifer: Column studies

Water quality changes associated with the passage of aerobic reverse osmosis (RO) treated recycled water through a deep anaerobic pyritic aquifer system was evaluated in sediment-filled laboratory columns as part of a managed aquifer recharge (MAR) strategy. The fate of nine recycled water trace organic compounds along with potential negative water quality changes such as the release of metal(loid)s were investigated in large-scale columns over a period of 12 months.The anaerobic geochemical conditions provided a suitable environment for denitrification, and rapid (half-life <1-25 days) degradation of the endocrine disrupting compounds (bisphenol A, 17β-estradiol, 17α-ethynylestradiol), and iodipamide. However, pharmaceuticals (carbamazepine and oxazepam), disinfection by-products (N-nitrosodimethylamine, N-nitrosomorpholine) and iohexol did not degrade rapidly (half-life > 100 days).High retardation coefficients (R) determined for many of the trace organics (R 13 to 67) would increase aquifer residence time and be beneficial for many of the slow degrading compounds. However, for the trace organics with low R values (1.1-2.6) and slow degradation rates (half-life > 100 days), such as N-nitrosodimethylamine, N-nitrosomorpholine and iohexol, substantial biodegradation during aquifer passage may not occur and additional investigations are required.Only minor transient increases in some metal(loid) concentrations were observed, as a result of either pyrite oxidation, mineral dissolution or pH induced metal desorption, followed by metal re-sorption downgradient in the oxygen depleted zone.     

Environmental oil pollution: a possible cause for the incidence of ankylosis,kyphosis, lordosis and scoliosis in five fish species collected from the vicinity of Jubail City,Saudi Arabia,Arabian Gulf

Spinal deformities such as scoliosis (lateral curvature), lordosis (ventral curvature), kyphosis (dorsal curvature) and ankylosis (fusion of vertebrae) have been described in many species both cultured and from the wild population. Specimens of Epinephelus tauvina, Siganus canaliculatus, Argyrops spinifer, Scomberomorus guttatus and Lethrinus nebulosus were used in this study. Four out of five deformed specimens showed abnormalities in the caudal region of the vertebral column. The specimen of E. tauvina showed the most acute deformity among the cases studied. All cases were not fatal as they occurred in adult individuals. The paper discusses the possible causes for such deformities as well as the suitability of this kind of study for environmental monitoring.     

Evaluation of a photocatalytic reactor membrane pilot system for the removal of pharmaceuticals and endocrine disrupting compounds from water

A photocatalytic reactor membrane pilot system, employing UV/TiO₂ photocatalysis, was evaluated for its ability to remove thirty-two pharmaceuticals, endocrine disrupting compounds, and estrogenic activity from water. Concentrations of all compounds decreased following treatment, and removal followed pseudo-first-order kinetics as a function of the amount of treatment. Twenty-nine of the targeted compounds in addition to total estrogenic activity were greater than 70% removed while only three compounds were less than 50% removed following the highest level of treatment (4.24 kW h/m³). No estrogenically active transformation products were formed during treatment. Additionally, the unit was operated in photolytic mode (UV only) and photolytic plus H₂O₂ mode (UV/H₂O₂) to determine the relative amount of energy required. Based on the electrical energy per order (EEO), the unit achieved the greatest efficiency when operated in photolytic plus H₂O₂ mode for the conditions tested.