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Reverse osmosis concentrate (ROC) produced as the by-product of the reverse osmosis process consists of a high load of organics (macro and micro) that potentially cause eco-toxicological effects in the environment. Previous studies focused on the removal of such compounds using oxidation, adsorption, and membrane-based treatments. However, these methods were not always efficient and formed toxic by-products. The impact of ion-exchange resin (IEX) (Purolite®A502PS) was studied in a micro-filtration-IEX hybrid system to remove organics from ROC for varying doses of Purolite® A502PS (5-20 g/L) at a flux of 36 L/m2h. The purolite particles in the membrane reactor reduced membrane fouling, evidenced by the reduction of transmembrane pressure (TMP), by pre-adsorbing the organics, and by mechanically scouring the membrane. The dissolved organic carbon was reduced by 45-60%, out of which 48-81% of the hydrophilics were removed followed by the hydrophobics and low molecular weight compounds (LMWs). This was based on fluorescence excitation-emission matrix and liquid chromatography-organic carbon detection. Negatively charged and hydrophobic organic compounds were preferentially removed by resin. Long-term experiments with different daily replacements of resin are suggested to minimize the resin requirements and energy consumption.

Natural organic matter (NOM) represents a range of soluble and insoluble material which can have considerable impact on drinking water quality. In addition to creating problems with taste, odour, clarification, and colour, removal of NOM is problematic because it can initiate the formation of disinfection by-products, which can adversely affect human health. Numerous technologies and methods have been employed to remove NOM in water treatment, with the most common processes involving the use of coagulants and similar technologies. This paper provides an overview of the most widely studied coagulants, coagulant aids, dual coagulants, and alternative coagulants. The paper also investigates the effects of operating parameters such as temperature, coagulant dose, pH, use of inorganic salts, inorganic polymeric coagulants, and organic polyelectrolytes in terms of charge neutralisation, polymer adsorption, and polymer bridging. Finally, emerging technologies and the use of novel coagulants are investigated.

Microbial pathogens present in stormwater, which originate from human sewage and animal faecal matters, are one of the major impediments in stormwater reuse. The transport of microbes in stormwater is more than just a physical process. The mobility of microbes in stormwater is governed by many factors, such as dissolved organic matter, cations, pH, temperature and water flow. This paper examined the roles of three environmental variables, namely: dissolved organic matter, positive cations and stormwater flow on the transport of two faecal indicator bacteria (FIB), Enterococcus spp. and Escherichia coli. Stormwater runoff samples were collected during twelve wet weather events and one dry weather event from a medium density residential urban catchment in Brisbane. Enterococcus spp. numbers as high as 3 × 104 cfu/100 mL were detected in the stormwater runoff, while Escherichia coli numbers up to 3.6 × 103 cfu/100 mL were observed. The dissolved organic carbon (DOC) in the stormwater samples was in the range of 2.2–5.9 mg/L with an average concentration of 4.5 mg/L in which the hydrophilic carbon constituted the highest mass fraction of 60–80%. The results also showed that the transport of FIB in stormwater was reduced with an increasing concentration of the hydrophilic organic fraction, especially the humic fraction. On the contrary, the concentration of trivalent cations and stormwater flow rate showed a positive correlation with the FIB numbers. These findings indicated the potentiality to make a good use and measurement of simple environmental variables to reflect the degree of microbe transport in stormwater from residential/suburban catchments.

Increased iron levels and dysregulated iron homeostasis, or both, occur in several lung diseases. Here, the effects of iron accumulation on the pathogenesis of pulmonary fibrosis and associated lung function decline was investigated using a combination of murine models of iron overload and bleomycin-induced pulmonary fibrosis, primary human lung fibroblasts treated with iron, and histological samples from patients with or without idiopathic pulmonary fibrosis (IPF). Iron levels are significantly increased in iron overloaded transferrin receptor 2 (Tfr2) mutant mice and homeostatic iron regulator (Hfe) gene-deficient mice and this is associated with increases in airway fibrosis and reduced lung function. Furthermore, fibrosis and lung function decline are associated with pulmonary iron accumulation in bleomycin-induced pulmonary fibrosis. In addition, we show that iron accumulation is increased in lung sections from patients with IPF and that human lung fibroblasts show greater proliferation and cytokine and extracellular matrix responses when exposed to increased iron levels. Significantly, we show that intranasal treatment with the iron chelator, deferoxamine (DFO), from the time when pulmonary iron levels accumulate, prevents airway fibrosis and decline in lung function in experimental pulmonary fibrosis. Pulmonary fibrosis is associated with an increase in Tfr1+ macrophages that display altered phenotype in disease, and DFO treatment modified the abundance of these cells. These experimental and clinical data demonstrate that increased accumulation of pulmonary iron plays a key role in the pathogenesis of pulmonary fibrosis and lung function decline. Furthermore, these data highlight the potential for the therapeutic targeting of increased pulmonary iron in the treatment of fibrotic lung diseases such as IPF. © 2020 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Accumulating evidence highlights links between iron regulation and respiratory disease. Here, we assessed the relationship between iron levels and regulatory responses in clinical and experimental asthma.We show that cell-free iron levels are reduced in the bronchoalveolar lavage (BAL) supernatant of severe or mild-moderate asthma patients and correlate with lower forced expiratory volume in 1 s (FEV1). Conversely, iron-loaded cell numbers were increased in BAL in these patients and with lower FEV1/forced vital capacity (FVC) ratio. The airway tissue expression of the iron sequestration molecules divalent metal transporter 1 (DMT1) and transferrin receptor 1 (TFR1) are increased in asthma, with TFR1 expression correlating with reduced lung function and increased Type-2 (T2) inflammatory responses in the airways. Furthermore, pulmonary iron levels are increased in a house dust mite (HDM)-induced model of experimental asthma in association with augmented Tfr1 expression in airway tissue, similar to human disease. We show that macrophages are the predominant source of increased Tfr1 and Tfr1+ macrophages have increased Il13 expression. We also show that increased iron levels induce increased pro-inflammatory cytokine and/or extracellular matrix (ECM) responses in human airway smooth muscle (ASM) cells and fibroblasts ex vivo and induce key features of asthma in vivo, including airway hyper-responsiveness (AHR) and fibrosis, and T2 inflammatory responses.Together these complementary clinical and experimental data highlight the importance of altered pulmonary iron levels and regulation in asthma, and the need for a greater focus on the role and potential therapeutic targeting of iron in the pathogenesis and severity of disease.

© 2018 Springer-Verlag GmbH Germany, part of Springer Nature The occurrence and fate of five drugs of abuse in raw influent and treated effluent wastewater were investigated over a period of 1 year in the Adelaide region of South Australia. Four wastewater treatment plants were chosen for this study and monitored for five drugs which included cocaine in the form of its metabolite benzoylecgonine (BE), methamphetamine, 3,4-methylenedioxymethamphetamine (MDMA) and two opioids (codeine and morphine) during the period April 2016 to February 2017. Alongside concentrations in raw sewage, the levels of drugs in the treated effluent were assessed and removal efficiencies were calculated. Drug concentrations were measured by mixed-mode solid phase extraction and liquid chromatography coupled to a quadrupole mass spectrometer. Drug concentrations detected in the raw wastewater ranged from 7 to 6510 ng/L and < LOD to 4264 ng/L in treated effluent samples. Drug removal rates varied seasonally and spatially. The mass loads of drugs discharged into the environment were in descending order: codeine > methamphetamine > morphine > MDMA > BE. Results showed that all the targeted drugs were on average incompletely removed by wastewater treatment, with removal performance highest for morphine (94%) and lowest for MDMA (58%). A screening-level environmental risk assessment was subsequently performed for the drugs based on effluent wastewater concentrations. Based on calculated risk quotients, overall environmental risk for these compounds appears low, with codeine and methamphetamine likely to pose the greatest potential risk to receiving environments. Given the recognised limitations of current ecotoxicological models and risk assessment methods for these and other pharmaceutical drugs, the potential for environmental impacts associated with the continuous discharge of these compounds in wastewater effluents should not be overlooked.

© 2019 Elsevier Ltd Assessing urban stormwater quality by investigation and characterisation of pollutants is a prerequisite for its effective management, for reuse and safe discharge. The stochastic nature of rainfall, dry weather periods, topology, human activities and climatic conditions generate and wash-off pollutants differently from event to event. This study investigated the major physico-chemical pollutants in stormwater runoff collected from an urban catchment over a period of two years. The aim of this study was to explore the use of UV spectroscopy to identify the first flush. In this study, the variation of pollutants during the passage of a rain event and the relationships among the measured pollutants was analysed to help broaden the application of UV spectroscopy beyond the detection of organic matter. Correlation analysis and principal component analysis (PCA) were performed to identify the possible relationship among measured pollutants. Although correlation analysis revealed some relationships between pollutants, in general they were not strong enough and was not helpful. PCA biplots suggested a few groups and revealed that the two components model could explain nearly 72% of the variability between pollutants. Pollutants in the group that included dissolved organic carbon (DOC) behaved in a similar manner. UV spectroscopy was applied to identify the first flush by comparing the recorded spectrum of consecutive samples that were collected in an event. Analysis of the spectra was able to isolate the point when first flush ends for DOC and pollutants that behave similar to it.

One of the key challenges in water treatment industry is the removal of organic compounds by cost-effective methods. This study evaluated the adsorptive removal of dissolved organic carbon (DOC) from reservoir water using fuller’s earth (FE) in comparison with natural (SQ) and modified quartz (MSQ) sands. The removal capacities of FE at different contact times, pH levels, adsorbent dosages and initial DOC concentrations were compared with both the quartz sands. The optimum DOC removals by FE and SQs were achieved at contact time of 60 and 30 min, pH level of 6 and 4, and at adsorbent dose of 1.5 g/150 mL and 10 g/100 mL, respectively. The adsorption capacity of FE (1.05 mg/g) was much higher compared to the MSQ (0.04 mg/g) and SQ (0.01 mg/g). Adsorption equilibrium data better fitted to the Freundlich model than to the Langmuir model, suggesting that adsorption occurred primarily through multilayer formation onto the surfaces of FE and SQ. The pseudo-second-order model described the uptake kinetics more effectively than the pseudo-first-order and intra-particle diffusion models, indicating that the mechanism was primarily governed by chemisorption. These observations were well supported by the physiochemical characteristics and charge behaviour of the adsorbents. In mass-transfer study, the results of liquid film diffusion model showed that the adsorption of DOC on FE was not controlled by film diffusion, but other mechanisms also played an essential role. This study demonstrates that FE is an effective adsorbent for the removal of DOC in surface water treatment.

© 2018 Elsevier Ltd Fluorescence excitation-emission matrix spectroscopy coupled with parallel factor analysis (FEEM/PARAFAC) was applied to characterise natural organic matter (NOM) present in nitrified and non-nitrified waters from different sampling sites in a drinking water distribution system in Australia. Each excitation-emission matrix (EEM) data set of nitrified and non-nitrified water samples were successfully decomposed into a three component PARAFAC model (C-1, C-2, and C-3). The spectral shapes of these components were compared with those identified earlier in other studies from the OpenFluor database. While C-1 and C-2 exhibited similar fluorescence spectra in both non-nitrified and nitrified sampling locations, there were some fluorescence peaks in C-3 for nitrified water samples that were not present in non-nitrified water samples. Both C-1 and C-2 in each PARAFAC model for nitrified and non-nitrified water samples showed striking similarities with components previously listed as humic-like compounds. While C-3 for non-nitrified water samples also consisted of terrestrial humic-like compounds, C-3 in PARAFAC model for nitrified water samples represented protein-like material produced as a result of microbiological activity. The fluorescence peaks that appeared only in nitrified sampling locations are related to the formation of microbial-like compounds associated with nitrification. These results indicate that PARAFAC modelling of EEM data can be used to investigate nitrification and water quality changes in chloraminated drinking water distribution systems.

© Taiwan Association for Aerosol Research. Australia commonly experiences extensive wildfires, mostly during its hot dry summers. These often lead to a significant loss of life and property. The October 2013 Blue Mountains Fire burnt through more than 100,000 hectares and generated a large amount of fire dust that was transported to the downwind community residing in the Sydney metropolitan area, which is the largest city in Australia. Record-breaking temperatures in New South Wales and strong winds worsened the wildfire danger index, and the extensive fires that broke out by 17th October lasted for more than a week. Analysis of the particulate matter monitored by the New South Wales Environmental Protection Authority around the fire zone showed that the concentrations of PM10 and PM2.5 increased by more than twofold (> 200%) and remained high for a week. During the peak fire period, SOx, NOx and O3 concentrations increased by 52%, 29% and 42%, respectively, above the usual levels recorded in metropolitan Sydney. The increase in the concentrations of these air contaminants in the Sydney metropolitan region over such an extended period may have caused increased human health risks, which are also examined in this paper.

© 2017, Springer-Verlag GmbH Germany. Chromium from tannery waste dump site causes significant environmental pollution affecting surrounding flora and fauna. The primary aims of this study were to survey vegetation, investigate the degree of soil pollution occurring near tannery waste dump site and make a systematic evaluation of soil contamination based on the chromium levels found in plants and earthworms from the impacted areas. This paper presents the pollution load of toxic heavy metals, and especially chromium, in 10 soil samples and 12 species of plants. Soil samples were analysed for heavy metals by using ICP-MS/ICP-OES method. Results indicated that Cr in soils exceeded soil quality guideline limits (SQGL). The total chromium present in the above ground parts of plants ranged from 1.7 mg kg−1 in Casuarina sp. to 1007 mg kg−1 in Sonchus asper. The Cr bioaccumulation in Eisenia fetida from tannery waste soil ranged from 5 to 194 mg kg−1. The high enrichment factor of Cr in S. asper and bioaccumulation factor in earthworms indicate that there is a steady increase of toxic chromium risk in this area, which could be correlated with the past dumping activity. Emphasis needs to be put on control measures of pollution and remediation techniques in such areas to achieve an ecologically sustainable industrialisation.

© 2017, Islamic Azad University (IAU). One of the key challenges in water treatment industry is the removal of organic compounds by cost-effective methods. This study evaluated the adsorptive removal of dissolved organic carbon (DOC) from reservoir water using fuller’s earth (FE) in comparison with natural (SQ) and modified quartz (MSQ) sands. The removal capacities of FE at different contact times, pH levels, adsorbent dosages and initial DOC concentrations were compared with both the quartz sands. The optimum DOC removals by FE and SQs were achieved at contact time of 60 and 30 min, pH level of 6 and 4, and at adsorbent dose of 1.5 g/150 mL and 10 g/100 mL, respectively. The adsorption capacity of FE (1.05 mg/g) was much higher compared to the MSQ (0.04 mg/g) and SQ (0.01 mg/g). Adsorption equilibrium data better fitted to the Freundlich model than to the Langmuir model, suggesting that adsorption occurred primarily through multilayer formation onto the surfaces of FE and SQ. The pseudo-second-order model described the uptake kinetics more effectively than the pseudo-first-order and intra-particle diffusion models, indicating that the mechanism was primarily governed by chemisorption. These observations were well supported by the physiochemical characteristics and charge behaviour of the adsorbents. In mass-transfer study, the results of liquid film diffusion model showed that the adsorption of DOC on FE was not controlled by film diffusion, but other mechanisms also played an essential role. This study demonstrates that FE is an effective adsorbent for the removal of DOC in surface water treatment.

We previously demonstrated elevated brain iron levels in myelinated structures and associated cells in a hemochromatosis Hfe−/−xTfr2mut mouse model. This was accompanied by altered expression of a group of myelin-related genes, including a suite of genes causatively linked to the rare disease family ‘neurodegeneration with brain iron accumulation’ (NBIA). Expanded data mining and ontological analyses have now identified additional myelin-related transcriptome changes in response to brain iron loading. Concordance between the mouse transcriptome changes and human myelin-related gene expression networks in normal and NBIA basal ganglia testifies to potential clinical relevance. These analyses implicate, among others, genes linked to various rare central hypomyelinating leukodystrophies and peripheral neuropathies including Pelizaeus-Merzbacher-like disease and Charcot-Marie-Tooth disease as well as genes linked to other rare neurological diseases such as Niemann-Pick disease. The findings may help understand interrelationships of iron and myelin in more common conditions such as hemochromatosis, multiple sclerosis and various psychiatric disorders.

Membrane fouling is linked to reversible or irreversible accumulation of macromolecules and solids on membrane surfaces and to the irreversible adsorption inside pores. If reversible accumulation can be controlled by filtering in subcritical conditions, then adsorption could also be minimized by reducing the soluble organic matter [extracellular polymeric substances, soluble microbial products (SMP)]. This research shows how the choice of operating parameters related to biological reaction (solid retention time and the organic loading rate) can influence the process rate and the by-product (SMP) production. It also illustrates how suspension characteristics and membrane aeration can influence membrane fouling control according to the hollow fiber configuration and to the different scales of observation. The investigations were based on the definition of different fouling level and fine-tuning of a model to better understand the effects of operating parameters on membrane bioreactor filtration.

Stormwater runoff from urban and industrial areas contains several types of heavy metals that have negative ecological impacts on receiving waters, and therefore methods need to be developed to remove these pollutants. Combined removal of a mixture of heavy metal cations (Cu 2+, Zn 2+, Cd 2+, and Ni 2+) and an oxy anion (selenate, SeO 4-) from an artificially prepared stormwater was investigated by sorption of these heavy metals on hydrous ferric oxide (HFO) in a column experiment under intermittent runoff (wetting and drying) condition, as occurs between rainfall events in the field. The heavy metal removal behaviour varied between ions as well as with time. In each continuous column run (8 h) the amount of ions removed progressively decreased with time and reached a constant level at approximately 4-6 h. However, stopping the runoff for 40 h and starting the next runoff after this period removed a large quantity of heavy metals in the first few hours of this run. The intermittent runoff for seven runs showed that HFO has a high capacity to remove copper and zinc, which were present in higher concentrations in the stormwater than cadmium, nickel and selenium.

The influence of hydraulic retention time (HRT) in a submerged hollow fibre membrane bioreactor was studied by conducting experiments at four different HRTs (4, 2, 1.3 and 1h) at room temperature of 25°C. It was found that a shorter HRT led to a higher development of trans-membrane pressure. The highest sludge cake and pore-blocking resistances of 4.02×10 11m -1 and 0.77×10 11m -1 respectively were noted for the shortest HRT (of 1h) application. UV and fluorescence spectroscopy analyses showed that the nature of organics in the biomass and sludge cakes were different. The organic fraction analysis by liquid chromatography with organic carbon detector (LC-OCD) showed a significant amount of biopolymers and a lower amount of humics for longer HRT. © 2011 Elsevier B.V.

Urban stormwater runoff, which consists of inorganic and organic contaminants, is a major source of pollutants to receiving waters and therefore they need to be removed. Simultaneous removal of contaminants, Cd2+, Cu2+, Ni2+, Zn2+ (heavy metal cations), and SeO42- (oxyanion) from a simulated stormwater by a hydrous ferric oxide (HFO) was studied in batch and column sorption experiments. In the batch experiment the rate of sorption of the ions was rapid at the beginning and reached equilibrium in approximately 300 min. The amounts of ions sorbed were proportionate to the respective initial concentration of the ions added to the HFO. Cluster analysis showed that all heavy metals had similar sorption behavior, whereas Se had a distinctly different sorption process. Of the three different kinetic models tested the pseudo-first order kinetic model fitted the data the best. The column experimental results beyond 180 min were consistent with those of the batch experiment that the removal efficiencies of the ions were in proportion to the ion concentration in the feed. Below 180 min, Cu appeared to be preferentially removed than Zn. © 2011 Korean Institute of Chemical Engineers, Seoul, Korea.

Recent advances in membrane technology have led to its broad application, and reverse osmosis (RO) systems now represent the fastest growing segment of the desalination market. Its performance is hindered by membrane fouling. In this study pre-treatment methods to reduce RO fouling were investigated including flocculation, adsorption and ion exchange. Detailed organic characterisations were made in terms of florescence spectroscopy excitation emission matrix (EEM), UV254 absorbance and liquid chromatography-organic carbon detection (LCOCD). The different pre-treatment methods were assessed in terms of the fouling potential. This was quantified in terms of the modified fouling index measured using a dead-end cell micro-filtration (MF) unit. The existing pre-treatment of granular activated carbon (GAC) filter led to a good organic removal. Among the pre-treatment methods tested in the laboratory, purolite ion exchange/adsorption was found to be better than FeCl3 flocculation in terms of the amount as well as the wide range of organics removal. A pre-treatment of flocculation with Poly-ferric-silicate (PFSi) as flocculent gave a higher removal of organic matter compared to other pre-treatments tested. DOC was reduced from 11.5 to 4.25 mg/L, and it removed mostly the humic type substances.

In this study, the SMBR was compared in terms of membrane fouling with and without the addition of suspended medium in the membrane reactor. The effectiveness of medium in suspension in submerged membrane bioreactor (SMBR) was evaluated at different filtration flux. The SMBR was operated at a flux of 5-30L/m2h (corresponding hydraulic retention time of 10-1.7h) with and without suspended medium. The suspended medium used in this study was granular activated carbon (GAC; particle size 300-600mm) at air scouring (aeration) rates of 0.5-1.5m3m-2 membrane areah-1. At higher aeration rate of 1.5m3/m2 membrane areah, the effect of flux on membrane resistance was found to be negligible. The reduction of aeration rate from 1.5 to 1.0m3m-2 membrane areah-1 resulted in a sudden rise of TMP. The addition of suspended medium prevented a sudden rise of TMP (total membrane resistance reduced from 51×1011 to 20×1011m-1). The organic removal efficiency remained high irrespective of flux. The molecular weight distribution (MWD) and excitation emission matrix (EEM) analysis of SMBR effluent showed a range of organic (composed of amino acids, biopolymers, humics and fulvic acids type substances) removed by the GAC both by scouring and adsorption mechanisms. © 2011 Elsevier B.V.