27 research outputs found

    Direct contact ultrasound for fouling control and flux enhancement in air-gap membrane distillation

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    © 2019 Elsevier B.V. Air Gap Membrane distillation (AGMD) is a thermally driven separation process capable of treating challenging water types, but its low productivity is a major drawback. Membrane fouling is a common problem in many membrane treatment systems, which exacerbates AGMD's low overall productivity. In this study, we investigated the direct application of low-power ultrasound (8–23 W), as an in-line cleaning and performance boosting technique for AGMD. Two different highly saline feedwaters, namely natural groundwater (3970 μS/cm) and RO reject stream water (12760 μS/cm) were treated using Polytetrafluoroethylene (PTFE) and polyvinylidene fluoride (PVDF) membranes. Theoretical calculations and experimental investigations are presented, showing that the applied ultrasonic power range only produced acoustic streaming effects that enhanced cleaning and mass transfer. Attenuated Total Reflection Fourier-Transform Infrared Spectroscopy (ATR FT-IR) analysis showed that ultrasound was capable of effectively removing silica and calcium scaling. Ultrasound application on a fouled membrane resulted in a 100% increase in the permeate flux. Cleaning effects accounted for around 30–50% of this increase and the remainder was attributed to mass transfer improvements. Contaminant rejection percentages were consistently high for all treatments (>99%), indicating that ultrasound did not deteriorate the membrane structure. Scanning Electron Microscopy (SEM) analysis of the membrane surface was used to confirm this observation. The images of the membrane surface demonstrated that ultrasound successfully cleaned the previously fouled membrane, with no signs of structural damage. The results of this study highlight the efficient and effective application of direct low power ultrasound for improving AGMD performance

    Ecological and human health risk assessment of polycyclic aromatic hydrocarbons (PAH) in Tigris river near the oil refineries in Iraq

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    Recent Iraqi battles against ISIS in 2014 and 2015 resulted in the destruction or severe damage to several refineries' infrastructure. This, along with other factors, has led to the release and accumulation of a wide range of hazardous chemicals into the environment, for instance, polycyclic aromatic hydrocarbons (PAH). Thus, for the first time, a comprehensive 16 PAHs measurements campaign over the course of six months near the oil refineries along the Tigris River and its estuaries was investigated. The 16 PAHs concentrations in surface water and the sediments for the following oil refineries: Baiji, Kirkuk, Al-Siniyah, Qayyarah, Al-Kasak, Daura, South Refineries Company, and Maysan were examined. The overall findings indicated that the 16 PAHs concentrations ranged from 567.8 to 3750.7 ng/L for water and 5619.2–12795.0 ng/g for sediment. Water samples in South Refineries Company recorded the highest PAH concentrations while Baiji oil refinery registered the highest PAH concentrations in the sediment samples. The percentages of high molecular weight PAH (5–6 rings) in water and sediment samples were the highest, ranging from 49.41% to 81.67% and from 39.06% to 89.39% of total PAH for water and sediment, respectively. The majority of 16 PAHs measured in water and sediment samples of the Tigris River were derived from pyrogenic sources. Based on sediment quality guidelines (SQGs), most sites showed a possible effect range with occasional biological effects of most of the PAH concentrations in all sediments’ samples. The calculated incremental lifetime cancer risk (ILCR) value was high risk with adverse health effects, including cancer

    Impact of hydrodynamic conditions on optimum power generation in dual stage pressure retarded osmosis using spiral-wound membrane

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    The Dual Stage Pressure Retarded Osmosis technique is considered for power generation. The influence of feed flow rates, hydraulic pressure, and pressure drop on mass transfer and solute diffusion in a full-scale membrane model was investigated for the first time to maximize power generation. Dead Sea-seawater, Dead Sea-reverse osmosis brine, reverse osmosis brine-wastewater, and seawater-wastewater salinity gradient resources were investigated for power generation. Results revealed a 71.07% increase in the specific power generation due to the dual-stage pressure retarded osmosis process optimization using Dead Sea-seawater salinity gradient resources. The increase in the specific power generation due to the dual-stage pressure retarded osmosis optimization was 108.8%, 63.18%, and 133.54%, respectively, for Dead Sea-reverse osmosis brine, reverse osmosis brine-wastewater, and seawater-wastewater salinity gradient resources. At optimum operating conditions, using the dual-stage pressure retarded osmosis process as an alternative to the single pressure retarded osmosis process achieved up to a 22% increase in the energy output. Interestingly, the hydraulic pressure at optimum operating conditions was slightly higher than the average osmotic pressure gradients in the dual-stage pressure retarded osmosis process. The study also revealed that power generation in the dual-stage pressure retarded osmosis process operating at constant mass transfer and solute resistivity parameters was overestimated by 2.8%

    Removal of emerging pollutants from water using enzyme-immobilized activated carbon from coconut shell

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    This work reports the removal of diclofenac, amoxicillin, carbamazepine, and ciprofloxacin by utilizing three commercially available granular activated carbons (GACs) (Activated carbon, Silcarbon, and Donau) loaded with laccase. Adsorption was used to successfully immobilize laccase on the GACs, as revealed by scanning electron microscopy and energy dispersive X-ray analysis (SEM-EDX) and Fourier transform infrared spectroscopy (FTIR). In the three types of GACs tested, pH 5, 30 °C, and 2 mg mL−1 laccase content were found to be the optimum immobilization parameters. Laccase immobilization yields of 65.2%, 63.1%, and 62.9% were achieved with activated carbon, Silcarbon, and Donau respectively. The adsorption behaviors of the pharmaceuticals onto the tested activated carbons are best described as a spontaneous endothermic process that follows Langmuir isotherm and first-order kinetics. The reusability of the immobilized enzyme was evaluated using 2, 2′-azino-bis 3-ethylbenzothiazole-6-sulphonic acid (ABTS) as a substrate within six cycles for all adsorbents. In 120 mins, nearly a complete removal of the pharmaceutical compounds (50 mg L−1) was obtained in the case of activated carbon type and more than 90% for other adsorbent types when synergistic adsorption and enzymatic degradation were applied. With adsorption alone, 74% removal was obtained with activated carbon and < 56% for other adsorbents. The finding of this study suggests that biochar produced from coconut shell (same as the one used in this study) can effectively be used as a substrate and adsorbent for pharmaceutical removal. This enzymatic physical removal system has the potential to be applied on a large-scale

    Temporal and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in the Danube River in Hungary

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    The Danube is a significant transboundary river on a global scale, with several tributaries. The effluents from industrial operations and wastewater treatment plants have an impact on the river's aquatic ecosystem. These discharges provide a significant threat to aquatic life by deteriorating the quality of water and sediment. Hence, a total of 16 Polycyclic Aromatic Hydrocarbons (PAHs) compounds were analyzed at six locations along the river, covering a period of 12 months. The objective was to explore the temporal and spatial fluctuations of these chemicals in both water and sediment. The study revealed a significant fluctuation in the concentration of PAHs in water throughout the year, with levels ranging from 224.8 ng/L during the summer to 365.8 ng/L during the winter. Similarly, the concentration of PAHs in sediment samples varied from 316.7 ng/g in dry weight during the summer to 422.9 ng/g in dry weight during the winter. According to the Europe Drinking Water Directive, the levels of PAHs exceeded the permitted limit of 100 ng/L, resulting in a 124.8% rise in summer and a 265.8% increase in winter. The results suggest that the potential human-caused sources of PAHs were mostly derived from pyrolytic and pyrogenic processes, with pyrogenic sources being more dominant. Assessment of sediment quality standards (SQGs) showed that the levels of PAHs in sediments were below the Effect Range Low (ERL), except for acenaphthylene (Acy) and fluorene (Fl) concentrations. This suggests that there could be occasional biological consequences. The cumulative Individual Lifetime Cancer Risk (ILCR) exceeds 1/104 for both adults and children in all sites

    A sustainable nano-hybrid system of laccase@M-MWCNTs for multifunctional PAHs and PhACs removal from water, wastewater, and lake water

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    This study examined the use of modified multiwall carbon nanotubes (M-MWCNTs) with immobilized laccase (L@M-MWCNTs) for removing ciprofloxacin (Cip), carbamazepine (Cbz), diclofenac (Dcf), benzo[a]pyrene (Bap), and anthracene (Ant) from different water samples. The synthesized materials were characterized using an array of advanced analytical techniques. The physical immobilization of laccase onto M-MWCNTs was confirmed through Scanning electron microscope (SEM)-dispersive X-ray spectroscopy (EDS) analysis and Brunner-Emmet-Teller (BET) surface area measurements. The specific surface area of M-MWCNTs decreased by 65% upon laccase immobilization. There was also an increase in nitrogen content seen by EDS analysis asserting successful immobilization. The results of Boehm titration and Fourier transform infrared (FTIR) exhibited an increase in acidic functional groups after laccase immobilization. L@M-MWCNTs storage for two months maintained 77.8%, 61.6%, and 57.6% of its initial activity for 4 °C, 25 °C, and 35 °C, respectively. In contrast, the free laccase exhibited 55.3%, 37.5%, and 23.5% of its initial activity at 4 °C, 25 °C, and 35 °C, respectively. MWCNTs improved storability and widened the working temperature range of laccase. The optimum removal conditions of studied pollutants were pH 5, 25 °C, and 1.6 g/L of M-MWCNTs. These parameters led to >90% removal of the targeted pollutants for four treatment cycles of both synthetic water and spiked lake water. L@M-MWCNTs demonstrated consistent removal of >90% for up to five cycles even with spiked wastewater. The adsorption was endothermic and followed Langmuir isotherm. Oxidation, dehydrogenation, hydroxylation, and ring cleavage seem to be the dominant degradation mechanisms

    Removal of Pharmaceuticals from Water Using Laccase Immobilized on Orange Peels Waste-Derived Activated Carbon

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    The ongoing discharge of containments into the environment has raised concerns about the potential harm they pose to various organisms. In the framework of eliminating pharmaceutical chemicals from aqueous solutions, enzymatic degradation by laccase is an environmentally friendly option. In this investigation, laccase immobilized on biochar derived from agricultural waste (orange peels, OPs) was used for the first time to remove carbamazepine and diclofenac from aqueous media. Different characterizations, such as Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy and energy dispersive X-ray spectroscopy (SEM-EDS), X-Ray diffraction (XRD), specific surface area (SBET), Boehm titration, proximate and ultimate analysis, as well as the point of zero-charge (pHPZC) analysis, were used in this study. The immobilization of laccase results in enhanced stability with respect to storage, temperature, and pH compared to laccase in its free form. The findings showed that the ideal conditions for immobilization were a pH of 4, a temperature of 30 °C, and a laccase concentration of 4.5 mg/mL. These parameters led to an immobilization yield of 63.40%. The stability of laccase immobilized on biochar derived from orange peels (LMOPs) was assessed over a period of 60 days, during which they preserved 60.2% and 47.3% of their initial activities when stored at temperatures of 25 °C and 4 °C, respectively. In contrast, free laccase exhibited lower stability, with only 33.6% and 15.4% of their initial activities maintained under the same storage conditions. Finally, the use of immobilized laccase proved to be effective in eliminating these pollutants in up to five cycles. Upon comparing the two systems, namely LMOPs and modified orange peels (MOPs), it becomes apparent that LMOPs exhibit an estimated 20% improvement in removal efficiency. These results affirmed the viability of activated carbon derived from OPs as a cost-effective option for immobilizing laccase. This approach could potentially be further scaled up to effectively eliminate organic pollutants from water sources

    Personal exposure and inhalation doses to PM1 and PM2.5 pollution in Iraq: An examination of four transport modes

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    Particulate matter (PM) is a major indicator of urban air quality deterioration due to its impact on human health, atmospheric visibility and climate change. However, sufficient data on personal exposure to air pollution is still rare or unavailable in developing countries such as Iraq. Thus, this paper investigated the personal exposure and inhalation doses of PM1 and PM2.5 in Al-Hillah city, Iraq, for four common motorized transportation modes, namely open windows car, closed window car, bus, and motorbike. A portable monitoring device was used to collect the data during morning and afternoon hours in two main streets in the city. A t-test examination of the obtained results showed that the mean exposure concentration for both PM2.5 and PM1 were significantly different in the two streets form most of the transportation modes. The difference in the means of the measured PM1 and PM2.5 in the morning and afternoon trips were statistically significant for all the transportation modes except for bus in 60 street. This highlights the special and temporal variation of air pollution in the city. This is largely due the deteriorated infrastructure and lack of control policies in the city. Overall, PM2.5 and PM1 measured exposure concentrations were higher in the morning trips than in the afternoon ones. Regardless of the time or place of measurements, closed windows cars always had the lowest exposure concentrations to PM1 and PM2.5. The alarming observation in this study was the high levels of PM1 and PM2.5 that exceeded the recommended WHO limits, and were higher than the reported concentrations in the world bank database. The study findings present preliminary data on personal exposure concentrations and inhalation doses for travelers in Al-Hillah city, which can be utilized for global studies of air contamination in countries in similar situations as Iraq and for developing local control strategies

    Polycyclic aromatic hydrocarbons in the surface water and sediment along Euphrates River system: Occurrence, sources, ecological and health risk assessment

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    This study presented for the first time a comprehensive measurement campaign of 16 PAHs along the Euphrates River for five months, in both water and sediment samples. Our study revealed that the PAHs contamination increased along the flow direction due to the increasing non-point pollution and the return flows of agriculture. The 5–6 rings PAHs were dominant in water and sediment samples with an average of 42 % and 50 %, respectively. The diagnostic ratios of PAHs suggest that the pollution of these compounds originated mainly from petroleum product combustions. The carcinogenic PAHs formed 46 % and 55 % of the total measured compounds in water and sediment samples, respectively, which highlights potential ecological and human health risks. Based on sediment quality guidelines (SQGs), most sites exhibit an effect range between low and medium. The calculated incremental lifetime cancer risk (ILCR) for adult and children were in the 10−2–10−3 range, which is 3–6-fold higher than what was reported in the literature. These observations call for urgent attention from environmental authorities of countries sharing this key water source in Western Asia
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