Fate and transport of perfluoro- and polyfluoroalkyl substances including perfluorooctane sulfonamides in a managed urban water body

Transport and fate of perfluoro- and polyfluoroalkyl substances (PFASs) in an urban water body that receives mainly urban runoff was investigated. Water, suspended solids, and sediment samples were collected during the monsoon (wet) and inter-monsoon (dry) season at different sites and depths. Samples were analyzed for C7 to C12 perfluoroalkyl carboxylate homologues (PFCAs) (PFHpA, PFOA, PFNA, PFDA, PFUnA, PFDoA), perfluorohexane, perfluorooctane, and 6:2-fluorotelomer sulfonate (PFHxS, PFOS, and 6:2FtS, respectively), perfluorooctane sulfonamide (FOSA), N-ethyl FOSA (sulfluramid), N-ethyl sulfonamidoethanol (N-EtFOSE), and N-methyl and N-ethyl sulfonamidoacetic acid (N-EtFOSAA and N-MeFOSAA, respectively). Concentrations in wet samples were only slightly higher. The sum total PFAS (ΣPFAS) concentrations dissolved in the aqueous phase and sorbed to suspended solids (SS) ranged from 107 to 253 ng/L and 11 to 158 ng/L, respectively. PFOA, PFOS, PFNA, PFHxS, and PFDA contributed most (approximately 90 %) to the dissolved ΣPFASs. N-EtFOSA dominated the particulate PFAS burden in wet samples. K _D values of PFOA and PFOS calculated from paired SS and water concentrations varied widely (1.4 to 13.7 and 1.9 to 98.9 for PFOA and PFOS, respectively). Field derived K _D was significantly higher than laboratory K _D suggesting hydrophobic PFASs sorbed to SS resist desorption. The ΣPFAS concentrations in the top sedimentary layer ranged from 8 to 42 μg/kg and indicated preferential accumulation of the strongly sorbing long-chain PFASs. The occurrence of the metabolites N-MeFOSAA, N-EtFOSAA and FOSA in the water column and sediments may have resulted from biological or photochemical transformations of perfluorooctane sulfonamide precursors while the absence of FOSA, N-EtFOSA and 6:2FtS in sediments was consistent with biotransformation.     

Interactions between metal ions and the biopolymer in activated sludge: quantification and effects of system pH value

The quantification and effects of system pH value on the interactions between Pb(II) and the biopolymer in activated sludge were investigated. The biopolymer had two protein-like fluorescence peaks (Ex/Em = 280 nm/326–338 nm for peak A; Ex/Em = 220–230 nm/324–338 nm for peak B). The fluorescence intensities of peak B were higher than those of peak A. The fluorophores of both peaks could be largely quenched by Pb(II), and the quencher dose for peak B was about half of that for peak A. The modified Stern-Volmer equation well depicted the fluorescence quenching titration. The quenching constant (Ka) values for both peaks decreased with rising system pH value, and then sharply decreased under alkaline conditions. It could be attributed to that the alkaline conditions caused the reduction of available Pb(II) due to the occurrence of Pb(OH)₂ sediments. The Ka values of peak B were bigger than those for peak A at the same system pH values. Accordingly, the aromatic proteins (peak B) played a key role in the interactions between metal ions and the biopolymer.

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Factors affecting urban electricity consumption: a case study in the Bangkok Metropolitan Area using an integrated approach of earth observation data and data analysis

Environmental Science and Pollution Research - Urbanization induces shifts in surface environmental factors, including impervious surface expansion, green space loss, and temperature increase in...     

Arsenic-contaminated groundwater and its potential health risk: A case study in Long An and Tien Giang provinces of the Mekong Delta,Vietnam

Environmental Science and Pollution Research - The occurrence of arsenic (As) in groundwater (drilled well water) that were used for drinking, cooking, and personal hygiene and its risks to human...     

Use of an exchange method to estimate the association and dissociation rate constants of cadmium complexes formed with low-molecular-weight organic acids commonly exuded by plant roots

Organic acids released from plant roots can form complexes with cadmium (Cd) in the soil solution and influence metal bioavailability not only due to the nature and concentration of the complexes but also due to their lability. The lability of a complex influences its ability to buffer changes in the concentration of free ions (Cd); it depends on the association (, m mol s) and dissociation (, s) rate constants. A resin exchange method was used to estimate and (m mol s), which is the conditional estimate of depending on the calcium (Ca) concentration in solution. The constants were estimated for oxalate, citrate, and malate, three low-molecular-weight organic acids commonly exuded by plant roots and expected to strongly influence Cd uptake by plants. For all three organic acids, the and estimates were around 2.5 10 m mol s and 1.3 × 10 s, respectively. Based on the literature, these values indicate that the Cd- low-molecular-weight organic acids complexes formed between Cd and low-molecular-weight organic acids may be less labile than complexes formed with soil soluble organic matter but more labile than those formed with aminopolycarboxylic chelates.     

Enteric Viruses in a Large Waterborne Outbreak of Acute Gastroenteritis in Finland

In Nokia city about 450,000 l of treated sewage water was for 2 days allowed to run into the drinking water supplies of the city due to a personal error of one employee. Within the next 5 weeks about 1,000 people sought care at the municipal health centre or regional hospital because of gastroenteritis. Here we report the results of viral analyses performed by gene amplification assays from the earliest water and sewage samples as well as from close to 300 patient samples. The contaminating treated sewage was shown to harbour several enteric viruses known to cause acute gastroenteritis. Likewise, the drinking water sample was positive for noro-, astro-, rota-, entero- and adenoviruses. Noroviruses were also found in 29.8% of stool samples from affected patients, while astro-, adeno-, rota- and enteroviruses were detected in 19.7, 18.2, 7.5 and 3.7% of the specimens, respectively. An erratum to this article can be found at     

Simulation of retention and transport of copper,lead and zinc in a paddy soil of the Red River Delta,Vietnam

Heavy metal (HM) contaminations in the topsoil around handicraft villages with non-ferrous heavy metal recycling in the Red River Delta can impose serious threats to the subsoil as well as to the groundwater quality. This feature is very important for paddy soils due to relatively high leaching rates and the dissolution of Fe–Mn oxides under reducing conditions which can accelerate the amount of HM translocated to the subsoil and groundwater.The transport of Cu, Pb and Zn in paddy soils was simulated by numerical modeling of non-equilibrium solute transport with an adaptation of the Hydrus-1D model. For the simulation, a water layer on the soil surface was included, from which HM can infiltrate into the soil depending on the soil hydraulic properties. Sorption coefficients, obtained from batch experiments were used as input data for the simulations. Calculated leaching rates were compared with the binding forms of HM in the samples.The simulations show that leaching rates decrease in the order: Zn > Cu > Pb. This order is confirmed by the results of sequential extractions. Under constant flooded conditions at a water table of 20 cm, Cu, Pb and Zn were estimated to reach the soil depth of 1 m within 470, 495 and 370 days, respectively, emphasizing that reactive pollutants can reach groundwater in a relatively short time. A change of the water layer from 1 to 30 cm can accelerate the leaching rate of HM up to 36%. The hard pan layer was observed to induce a hysteresis in hydraulic conductivity and slow down the movement of HM. Uncertainties in modeling arise as several parameters in the simulation can be determined only with significant errors. However, Hydrus-1D is a suitable tool for simulation of the transport of HM in paddy soils.     

Biocatalytic polymeric membranes to decrease biofilm fouling and remove organic contaminants in wastewater: a review

The presence of recalcitrant contaminants in wastewater is major challenge to decrease pollution and associated health issues. As a consequence, membrane technologies have recently attracted industrial attention, yet a major setback of membrane employment is membrane fouling which leads to frequent discarding of membrane modules. More than 45% of all membrane fouling cases are caused by biofilms that are resistant to antimicrobial agents. Here we review polymeric membranes with antifouling properties, with focus on surface properties, fabrication, characterization, biocatalysis using enzymes and application towards the removal of dyes, phenol, pesticides and fertilizers. Nano-engineered fabrication of polymeric membranes allow to decrease fouling by 80–90%. Immobilized oxidoreductases in polymeric membranes allow 65–98% removal contaminants in wastewater.

     

Formation,antimicrobial activity,and biomedical performance of plant-based nanoparticles: a review

Environmental Chemistry Letters - Because many engineered nanoparticles are toxic, there is a need for methods to fabricate safe nanoparticles such as plant-based nanoparticles. Indeed, plant...     

Impact of Covid-19 partial lockdown on PM2.5, SO2, NO2, O3, and trace elements in PM2.5 in Hanoi,Vietnam

Covid-19 lockdowns have improved the ambient air quality across the world via reduced air pollutant levels. This article aims to investigate the effect of the partial lockdown on the main ambient air pollutants and their elemental concentrations bound to PM_2.5 in Hanoi. In addition to the PM_2.5 samples collected at three urban sites in Hanoi, the daily PM_2.5, NO₂, O₃, and SO₂ levels were collected from the automatic ambient air quality monitoring station at Nguyen Van Cu street to analyze the pollution level before (March 10th–March 31st) and during the partial lockdown (April 1st–April 22nd) with “current” data obtained in 2020 and “historical” data obtained in 2014, 2016, and 2017. The results showed that NO₂, PM_2.5, O₃, and SO₂ concentrations obtained from the automatic ambient air quality monitoring station were reduced by 75.8, 55.9, 21.4, and 60.7%, respectively, compared with historical data. Besides, the concentration of PM_2.5 at sampling sites declined by 41.8% during the partial lockdown. Furthermore, there was a drastic negative relationship between the boundary layer height (BLH) and the daily mean PM_2.5 in Hanoi. The concentrations of Cd, Se, As, Sr, Ba, Cu, Mn, Pb, K, Zn, Ca, Al, and Mg during the partial lockdown were lower than those before the partial lockdown. The results of enrichment factor (EF) values and principal component analysis (PCA) concluded that trace elements in PM_2.5 before the partial lockdown were more affected by industrial activities than those during the partial lockdown.