27,164 research outputs found

    Direct nanofiltration of wastewater treatment plant effluent

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    Membrane technology, especially nanofiltration, is seen as a suitable technology to polish WWTP effluent to EU WFD standards and consequently produce an effluent quality suitable for agricultural or (in)direct potable usage. The objective of this study was to assess the potential of direct nanofiltration as technique for effluent reclamation

    Influence of chemical speciation on the separation of metal ions from chelating agents by nanofiltration membranes

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    The simultaneous separation of various metal ions (nickel, copper, calcium, and iron) from chelating agents (EDTA and citric acid in water streams using Nanofiltration membranes is analyzed. Assuming that multiply-charged species are highly rejected, chemical speciation com-10 putations reproduce the observed patterns of metal and ligand rejection at different pH values and concentrations.Postprint (updated version

    Dairy waste water treatment by combining ozonation and nanofiltration

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    The aim of this investigation was to examine the applicability of the membrane technique and the effect of preozonation in dairy waste water treatment technology. The best degree of surfactant removal from model anionic surfactant solution by nanofiltration was achieved at 20 degrees C and 40 bar. Investigations on the effects of ozone treatment of the waste water indicated that preozonation decreased the flux and increased the chemical oxygen demand and surfactant removal efficiency. Ozone treatment enhanced the biodegradability of the retentate from 68.8% to 96.4%

    Trace ions rejection tunning in NF by selecting solution composition: Ion permeances estimation

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    Nanofiltration (NF) is suggested to selectively remove ionic species in aqueous process streams taking benefit of both membrane and aqueous solution composition. The importance of predicting and optimizing selective ion rejections by NF not only of major compounds (e.g. NaCl, Na2SO4, MgCl2, MgSO4) but also of minor ones such as ammonium (NH4+), nitrate (NO3-), bromide (Br-), iodide (I-) typically present in natural and industrial process streams is crucial. The current work explores ion rejection patterns and membrane ion permeances using the phenomenological Solution-Electro-Diffusion-Film (SEDF) model. It makes possible rapid calculations that account for the effects of spontaneously arising electric fields on rejections. Experimental ion rejection data of several inorganic ions species at various transmembrane pressures and at fixed cross-flow velocity have been obtained with NF270 membrane. A number of trace ions (Na+, K+, Cl-, Ca2+, Mg2+, SO42-, NO3-, NH4+, Br-and I-) have been used in combination with various dominant salts (NaCl, MgCl2, MgSO4) as model feed solutions. Results showed that dominant salts were moderately (NaCl) and highly (MgCl2, MgSO4) rejected when some ions are divalent, while trace ions exhibited quite variable rejection, including negative ones mainly at low transmembrane volume flows. The electric field of membrane potential can accelerate or retard the ion flows to the permeate, so negative or unexpectedly high rejections could be observed. Ions transport was shown to be affected by the membrane chemistry (e.g. acid-base properties of the un-crosslinked carboxylic and amine groups) and the dielectric exclusion phenomena. From the modelling procedure, ionic membrane permeances were determined for various multi-ion systems studied. Results showed that nature of dominant salt composition can be used to control the rejection of minor components.Peer ReviewedPostprint (author's final draft

    Dichloroaniline retention by nanofiltration membranes

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    This study evaluates the performance of two nanofiltration membranes in removing a herbicide: dichloroaniline. The membranes, one polyamide and one cellulose acetate, have a cut-off in the range 150–300 g/mol (manufacturers’ data). The experiments were carried out with solutions of dichloroaniline in demineralized water, with concentrations from 1 to 10 ppb. For each membrane, the amount of herbicide retained and adsorbed by the membrane was determined as a function of feed concentration and transmembrane pressure. The two membranes, made of different materials but having the same nominal cut-off, retained dichloroaniline to very different extents and by different mechanisms

    Investigation of nanofiltration as a purification step for lactic acid production processes based on conventional and bipolar electrodialysis operations

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    Nanofiltration was investigated for usability in a specific lactic acid production process based on conventional and bipolar electrodialysis operations. Industrial fluids, corresponding to two potential integration levels and coming from an existing installation, were investigated. The commercially available DK nanofiltration membrane was used and performances in terms of lactate/lactic acid recovery rate and purification efficiency are reported. Nanofiltration was able to efficiently remove magnesium and calcium ions from a sodium lactate fermentation broth before its concentration and conversion by electrodialysis (first potential integration level). Maximum impurities rejections and lactate recovery were obtained at maximum transmembrane pressures. Mg2+ and Ca2+ rejections were 64±7 and 72±7%, respectively and lactate recovery rate reached 25±2 molm−2 h−1 for P = 20 bar. Sulfate and phosphate ions were also partially removed from the broth (40% rejection). At the invert, chloride ions were negatively retained by the membrane and were consequently more concentrated in the permeate. Nanofiltration also led to a nearly total decolouration of the fermentation broth. On the other hand, sulfate and phosphate rejections obtained from the filtration of a converted broth containing the lactic acid under its neutral form (second potential integration level) were also satisfactory, i.e. 47±5 and 51±5%, respectively. High recovery rates were observed in that case, i.e. 48±2 molm−2 h−1 at 20 bar. It indicated that NF could also be used as final purification step in the process

    Fenton coupled with nanofiltration for elimination of Bisphenol A

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    Bisphenol A (BPA) is a typical Endocrine Disrupting Chemical (EDC), which is potentially harmful during wastewater reclamation. In this study, its degradation during Fenton's process under different operational conditions was investigated in combination with subsequent nanofiltration of low concentration remnant BPA and compounds derived from oxidation. The results indicate that BPA could be degraded efficiently in aqueous phase by Fenton, even at very low hydrogen peroxide doses. The treatment of up to 300 mg/L solutions of BPA with Fenton liquor at optimal conditions resulted in its complete removal in less than 2 min. The optimal conditions were found to be pH, = 3, H2O2/BPA = 020 and Fe2+/BPA = 0.012. Five NF polymeric membranes having different properties were used for the nanofiltration of treated and non-treated solutions. The nanofiltration of BPA solutions showed that rejection is related to adsorption ability of BPA on the membrane and size exclusion mechanism. In the nanofiltration of the effluent after Fenton oxidation, high TOC, COD, colour and Fe2+ (>77%) removal were achieved, although significant membrane fouling was also observed. The normalised water flux after membrane flushing with water was lower than 60% in almost all used membranes, which indicates significant non-easily removable fouling. (C) 2014 Elsevier B.V. All rights reserved.Peer ReviewedPostprint (author’s final draft

    Cyclophosphamide removal from water by nanofiltration and reverse osmosis membrane

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    The rejection of cyclophosphamide (CP) by nanofiltration (NF) and reverse osmosis (RO) membranes from ultrapure (Milli-Q) water and membrane bioreactor (MBR) effluent was investigated. Lyophilization–extraction and detection methods were first developed for CP analysis in different water matrices. Experimental results showed that the RO membrane provided excellent rejection (>90%) under all operating conditions. Conversely, efficiency of CP rejection by NF membrane was poor: in the range of 20–40% from Milli-Q water and around 60% from MBR effluent. Trans-membrane pressure, initial CP concentration and ionic strength of the feed solution had almost no effect on CP retention by NF. On the other hand, the water matrix proved to have a great influence: CP rejection rate by NF was clearly enhanced when MBR effluent was used as the background solution. Membrane fouling and interactions between the CP and water matrix appeared to contribute to the higher rejection of CP
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