5 research outputs found

    Minimum net driving temperature concept for membrane distillation

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    In this study, we analyzed the heat requirement of membrane distillation (MD) to investigate the trade-off between the evaporation efficiency and driving force efficiency in a single effect MD system. We found that there exists a non-zero net driving temperature difference that maximizes efficiency. This is the minimum net driving temperature difference necessary for a rational operational strategy because below the minimum net driving temperature, both the productivity and efficiency can be increased by increasing the temperature difference. The minimum net driving temperature has a similar magnitude to the boiling point elevation (~0.5 °C for seawater), and depends on the properties of the membrane and the heat exchanger. The minimum net driving temperature difference concept can be used to understand the occurrence of optimal values of other parameters, such as flux, membrane thickness, and membrane length, if these parameters are varied in a way that consequently varies the net driving temperature difference.BT/Environmental Biotechnolog

    Phosphonate removal from membrane concentrate by electro-coagulation

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    In this study, the efficiency of electrocoagulation (EC) with iron electrodes was applied to remove two phosphonates, 1-hydroxyethylidene-1, 1-diphosphonic acid (HEDP) and nitrilotris(methylene) triphosphonic acid (NTMP) from concentrates. This work provides a detailed description of the experimental procedure and results on phosphonate removal and recovery from different electrolytes, including synthetic and real reverse osmosis (RO) membrane concentrates. This research showed high selectivity of EC, removing 100% and 80% of the NTMP and the HEDP respectively, confirming no competition with sulfates, nitrates, or silica. When experimenting with other electrolytes, calcium showed to be critical in enhancing the flocculation process, while calcium carbonate precipitation contributed to capturing the phosphonates from the concentrate. The produced iron oxide (sludge) was confirmed as goethite and akaganéite, and finally transformed into hematite, indicating the oxidation from Fe2+ to Fe3+ during the EC process. After the iron precipitate collection, an alkaline wash of the sludge was enough to recover 100% of the initial phosphorus from the NTMP phosphonate. However, further research is needed to optimize the recovery procedure and to improve the results with the HEDP. 70 and 140 A·m-2 current densities were optimal to bring HEDP and NTMP concentrations down to 32 μM (1 mg·L-1) in only 30 and 10 min respectively. In these conditions, the operational costs, 1.10 and 0.03 €·m-3 of treated concentrate, were estimated for HEDP and NTMP respectively. Even when EC has been widely studied for phosphate removal, this technique has been barely applied to treat concentrates containing phosphonate-based antiscalants. EC opens new possibilities for phosphonates and phosphorus to be removed and recovered respectively from membrane and other concentrates. Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.BT/Environmental Biotechnolog

    Physicochemical Characterization of Two Protic Hydroxyethylammonium Carboxylate Ionic Liquids in Water and Their Mixture

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    A systematic study on the physicochemical properties of two protic ionic liquids (ILs) {2-hydroxyethylammonium acetate ([Mea][Ac]) and 2-hydroxyethylammonium hexanoate ([Mea][Hex])} and their mixtures with water was performed. The density and viscosity were assessed across the entire range of aqueous dilutions between 278 and 393 K. The conductivities, water activities, and surface tension of the binary systems in water were also assessed, and the influence of anions was evaluated. Differential scanning calorimetry (DSC), Fourier transform infrared (FTIR), and 1H and 13C nuclear magnetic resonance (NMR) techniques were used to study the systems at different IL compositions. The excess molar volumes (VE) and thermal expansion coefficients were calculated, with negative values for VE across the entire concentration range. Density data were fitted to a polynomial for density prediction, function of temperature, and concentration, with the average deviation percentage not exceeding 0.63%. The viscosities of the binary systems were studied considering six different models and were better predicted by the model of Herráez et al. at IL concentrations higher than 0.25 mole fraction. The systems containing [Hex]- exhibited higher water activities and lower conductivity and surface tension. All studied systems exhibited a glass transition event, which varied according to the IL composition. The FTIR and NMR analysis confirmed the distinct molecular arrangement of [Mea][Ac] and [Mea][Hex] systems. Green Open Access added to TU Delft Institutional Repository 'You share, we take care!' - Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.BT/Bioprocess EngineeringBT/Biocatalysi

    Effect of phosphate availability on biofilm formation in cooling towers

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    Phosphate limitation has been suggested as a preventive method against biofilms. P-limited feed water was studied as a preventive strategy against biofouling in cooling towers (CTs). Three pilot-scale open recirculating CTs were operated in parallel for five weeks. RO permeate was fed to the CTs (1) without supplementation (reference), (2) with supplementation by biodegradable carbon (P-limited) and (3) with supplementation of all nutrients (non-P-limited). The P-limited water contained ≤10 µg PO4 l−1. Investigating the CT-basins and coupons showed that P-limited water (1) did not prevent biofilm formation and (2) resulted in a higher volume of organic matter per unit of active biomass compared with the other CTs. Exposure to external conditions and cycle of concentration were likely factors that allowed a P concentration sufficient to cause extensive biofouling despite being the limiting compound. In conclusion, phosphate limitation in cooling water is not a suitable strategy for CT biofouling control.BT/Environmental Biotechnolog

    Pilot-scale assessment of urea as a chemical cleaning agent for biofouling control in spiral-wound reverse osmosis membrane elements

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    Routine chemical cleaning with the combined use of sodium hydroxide (NaOH) and hydrochloric acid (HCl) is carried out as a means of biofouling control in reverse osmosis (RO) membranes. The novelty of the research presented herein is in the application of urea, instead of NaOH, as a chemical cleaning agent to full-scale spiral-wound RO membrane elements. A comparative study was carried out at a pilot-scale facility at the Evides Industriewater DECO water treatment plant in the Netherlands. Three fouled 8-inch diameter membrane modules were harvested from the lead position of one of the full-scale RO units treating membrane bioreactor (MBR) permeate. One membrane module was not cleaned and was assessed as the control. The second membrane module was cleaned by the standard alkali/acid cleaning protocol. The third membrane module was cleaned with concentrated urea solution followed by acid rinse. The results showed that urea cleaning is as effective as the conventional chemical cleaning with regards to restoring the normalized feed channel pressure drop, and more effective in terms of (i) improving membrane permeability, and (ii) solubilizing organic foulants and the subsequent removal of the surface fouling layer. Higher biomass removal by urea cleaning was also indicated by the fact that the total organic carbon (TOC) content in the HCl rinse solution post-urea-cleaning was an order of magnitude greater than in the HCl rinse after standard cleaning. Further optimization of urea-based membrane cleaning protocols and urea recovery and/or waste treatment methods is proposed for full-scale applications.BT/Environmental Biotechnolog
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