Microbial community analysis of membrane bioreactor incorporated with biofilm carriers and activated carbon for nitrification of urine.

The integration of powdered activated carbon and biofilm carriers in a membrane bioreactor (MBR) presents a promising approach to address the challenge of long hydraulic retention time (HRT) for nitrification of hydrolysed urine. This study investigated the effect of the incorporation in the MBR on microbial dynamics, focusing on dominant nitrifying bacteria. The results showed that significant shifts in microbial compositions were observed with the feed transition to full-strength urine and across different sludge growth forms. Remarkably, the nitrite-oxidizing bacteria Nitrospira were highly enriched in the suspended sludge. Simultaneously, ammonia-oxidizing bacteria, Nitrosococcaceae thrived in the attached biomass, showing a significant seven-fold increase in relative abundance compared to its suspended counterpart. Consequently, the incorporated MBR displayed 36% higher nitrification rate and 40% HRT reduction compared to the conventional MBR. This study provides valuable insights on the potential development of household or building scale on-site nutrient recovery from urine to fertiliser.

Impact of source-separation of urine on treatment capacity, process design, and capital expenditure of a decentralised wastewater treatment plant.

In this study, the impact of urine diversion on the treatment capacity, treatment process, and capital costs of a decentralised wastewater treatment plant (WWTP) was simulated using BioWin. The data for simulation including for economic analysis were obtained from a real decentralised WWTP at Sydney. Simulation was conducted for two alternative process design scenarios of a WWTP: membrane bioreactor (MBR) without denitrification and anaerobic MBR in place of aerobic MBR and compared to existing process design. The simulation shows that with about 75% urine diversion (through source separation), the treatment capacity of the existing WWTP can be doubled although above 40% urine diversion, the impact appears less rapid. When the urine diversion exceeds 75%, it was found that the anoxic tank for biological denitrification becomes redundant and the current wastewater treatment process could be replaced with a simpler and much less aeration intensive membrane bioreactor (MBR) producing similar effluent quality with a 24% reduction in capital expenditure (footprint) cost. Anaerobic MBR can be a potential alternative to aerobic MBR although pre-treatment becomes essential before reverse osmosis treatment for water reuse applications. Sensitivity analysis has revealed that by operating the bioreactor at higher mixed liquor suspended solids concentrations (9 g/L instead of 5 g/L) could help increase the WWTP treatment capacity by about 3.5 times at 75% urine diversion. Hence, urine diversion (until nitrogen-limiting conditions occur above 75% urine diversion) can increase the treatment capacity of an existing WWTP and reduce the capital expenses due to reduced plant footprint.

Electrode for selective bromide removal in membrane capacitive deionisation.

Due to the shortage of freshwater around the world, seawater is becoming an important water source. However, seawater contains a high concentration of bromide that can form harmful disinfection by-products during water disinfection. Therefore, the current seawater reverse osmosis (SWRO) has to adopt two-pass reverse osmosis (RO) configuration for effective bromide removal, increasing the overall desalination cost. In this study, a bromide selective composite electrode was developed for membrane capacitive deionisation (MCDI). The composite electrode was developed by coating a mixture of bromide selective resin and anion exchange polymer on the surface of the commercial activated carbon electrode, and its performance was compared to that of conventional carbon electrode. The results demonstrated that the composite electrode has ten times better bromide selectivity than the conventional carbon electrode. The study shows the potential application of MCDI for the selective removal of target ions from water sources and the potential for resource recovery through basic modification of commercial electrode.

On-site domestic wastewater treatment system using shredded waste plastic bottles as biofilter media: Pilot-scale study on effluent standards in Bhutan.

In this study, a 1000 L/d capacity one-off on-site wastewater treatment system was operated for over a year as a pilot alternative to the conventional on-site treatment as currently used in urban Bhutan. An up-flow anaerobic sludge blanket (UASB) was used for blackwater treatment (to replace "septic tank followed by an anaerobic biofilter (ABF) (to replace soak pits) for the treatment of a mixture of greywater and UASB effluent. Shredded waste plastic bottles were used as the novel biofilter media in the ABF. During a yearlong operation, the pilot system produced a final treated effluent from ABF with average BOD5 28 mg/L, COD 38 mg/L, TSS 85 mg/L and 5 log units of Escherichia coli. These effluents met three out of four of the national effluent discharge limits of Bhutan, but unsuccessful to meet the Escherichia coli standard over a yearlong operation. Further, process optimisation may enable more significant Escherichia coli removal. An economic analysis indicates that the total unit cost (capital and operating expenditures) of this alternative wastewater treatment system for more than 50 users range between USD 0.27-0.37/person/month comparable to USD 0.29-0.42/person/month for the current predominant on-site system, i.e., "septic tanks". This pilot study, therefore, indicates that this wastewater treatment system using shredded waste plastic biofilter media has high potential to replace the current conventional treatment, i.e., "septic tanks", which are often overloaded with greywater and discharging effluents which does not meet the national standards.

Fertiliser recovery from source-separated urine via membrane bioreactor and heat localized solar evaporation.

Urine with its abundant macronutrients (N-P-K) is an ideal resource for the production of fertiliser. However, the odor and pathogens in the raw urine must be removed to meet the public acceptance of urine collection systems and to enable its safe reuse as a fertiliser. In this work, real urine was collected and treated through a pilot-scale gravity-driven membrane bioreactor (GDMBR) to remove the malodorous organics and to nitrify almost 50% of the ammonia into nitrate. The stablised urine was subsequently distilled via low-cost heat localized solar evaporation (HLSE) to produce a non-odorous solid fertiliser. The developed HLSE with a small footprint can attract bulk solution into a vertical insulated space and quickly heat it up to 68 °C within 1 h. The HLSE process had vapour flux at 1.3 kg m-2 h-1 as well as high solar to vapour conversion efficiency at 87%. Based on the EDX mapping and XRD analysis, the generated crystals are mainly NaNO3, NH4Cl, NaCl, NH4H2PO4 and K2HPO4, which are ideal nutrients for vegetation. In this study, the produced urine-derived fertilisers have a better performance on the growth of the leafy basil than the all-purpose commercial fertilisers. Generally, the GDMBR-HLSE is a promising cost-effective and green technology for nutrients recovery from urine.

Chemically Cross-Linked Graphene Oxide as a Selective Layer on Electrospun Polyvinyl Alcohol Nanofiber Membrane for Nanofiltration Application.

Graphene oxide (GO) nanosheets were utilized as a selective layer on a highly porous polyvinyl alcohol (PVA) nanofiber support via a pressure-assisted self-assembly technique to synthesize composite nanofiltration membranes. The GO layer was rendered stable by cross-linking the nanosheets (GO-to-GO) and by linking them onto the support surface (GO-to-PVA) using glutaraldehyde (GA). The amounts of GO and GA deposited on the PVA substrate were varied to determine the optimum nanofiltration membrane both in terms of water flux and salt rejection performances. The successful GA cross-linking of GO interlayers and GO-PVA via acetalization was confirmed by FTIR and XPS analyses, which corroborated with other characterization results from contact angle and zeta potential measurements. Morphologies of the most effective membrane (CGOPVA-50) featured a defect-free GA cross-linked GO layer with a thickness of ~67 nm. The best solute rejections of the CGOPVA-50 membrane were 91.01% for Na2SO4 (20 mM), 98.12% for Eosin Y (10 mg/L), 76.92% for Methylene blue (10 mg/L), and 49.62% for NaCl (20 mM). These findings may provide one of the promising approaches in synthesizing mechanically stable GO-based thin-film composite membranes that are effective for solute separation via nanofiltration.

Removal of pharmaceuticals from nitrified urine.

In this study, granular activated carbon (GAC) was examined for the removal of five of the most commonly detected pharmaceuticals (naproxen, carbamazepine, acetaminophen, ibuprofen and metronidazole) from a nitrified urine to make the urine-derived fertiliser nutrient safe for food crops. Batch experiments were conducted to investigate the adsorption kinetics that described the removal of micropollutants (equal concentrations of 0.2 mM) from the synthetic nitrified urine at different GAC dosages (10-3000 mg/L). Artificial neural network modelling was also used to predict and simulate the removal of pharmaceuticals from nitrified urine. Langmuir and Freundlich isotherm models described the equilibrium data, with the Langmuir model providing slightly higher correlations. At the highest dose of 3000 mg/L GAC, all the pharmaceuticals showed a removal rates of over 90% after 1 h of adsorption time and 99% removal rates after 6 h of adsorption time. This study concludes that GAC is able to remove the targeted xenobiotics without affecting the concentration of N and P in the urine, suggesting that nitrified urine could be safely used as a nutrient product in future.

Urine Treatment on the International Space Station: Current Practice and Novel Approaches.

A reliable, robust, and resilient water recovery system is of paramount importance on board the International Space Station (ISS). Such a system must be able to treat all sources of water, thereby reducing resupply costs and allowing for longer-term space missions. As such, technologies able to dewater urine in microgravity have been investigated by different space agencies. However, despite over 50 years of research and advancements on water extraction from human urine, the Urine Processing Assembly (UPA) and the Water Processor Assembly (WPA) now operating on the ISS still achieve suboptimal water recovery rates and require periodic consumables resupply. Additionally, urine brine from the treatment is collected for disposal and not yet reused. These factors, combined with the need for a life support system capable of tolerating even dormant periods of up to one year, make the research in this field ever more critical. As such, in the last decade, extensive research was conducted on the adaptation of existing or emerging technologies for the ISS context. In virtue of having a strong chemical resistance, small footprint, tuneable selectivity and versatility, novel membrane-based processes have been in focus for treating human urine. Their hybridisation with thermal and biological processes as well as the combination with new nanomaterials have been particularly investigated. This article critically reviews the UPA and WPA processes currently in operation on the ISS, summarising the research directions and needs, highlighted by major space agencies, necessary for allowing life support for missions outside the Low Earth Orbit (LEO). Additionally, it reviews the technologies recently proposed to improve the performance of the system as well as new concepts to allow for the valorisation of the nutrients in urine or the brine after urine dewatering.

Energy recovery through reverse electrodialysis: Harnessing the salinity gradient from the flushing of human urine.

Urine dilution is often performed to avoid clogging or scaling of pipes, which occurs due to urine's Ca2+ and Mg2+ precipitating at the alkaline conditions created by ureolysis. The large salinity gradient between urine and flushing water is, theoretically, a source of potential energy which is currently unexploited. As such, this work explored the use of a compact reverse electrodialysis (RED) system to convert the chemical potential energy of urine dilution into electric energy. Urine' composition and ureolysis state as well as solution pumping costs were all taken into account. Despite having almost double its electric conductivity, real hydrolysed urine obtained net energy recoveries ENet of 0.053-0.039 kWh/m3, which is similar to energy recovered from real fresh urine. The reduced performances of hydrolysed urine were linked to its higher organic fouling potential and possible volatilisation of NH3 due to its high pH. However, the higher-than-expected performance achieved by fresh urine is possibly due to the fast diffusion of uncharged urea to the freshwater side. Real urine was also tested as a novel electrolyte solution and its performance compared with a conventional K4Fe(CN)6/K3Fe(CN)6 couple. While K4Fe(CN)6/K3Fe(CN)6 outperformed urine in terms of power densities and energy recoveries, net chemical reactions seemed to have occurred in urine when used as an electrolyte solution, leading to TOC, ammonia and urea removal of up to 13%, 6% and 4.4%, respectively. Finally, due to the migration of K+, NH4+ and PO43-, the low concentration solution could be utilised for fertigation. Overall, this process has the potential of providing off-grid urine treatment or energy production at a household or building level.

Fouling and performance of outer selective hollow fiber membrane in osmotic membrane bioreactor: Cross flow and air scouring effects.

This study assessed impacts of cross-flow velocity (CFV) and air scouring on the performance and membrane fouling mitigation of a side-stream module containing outer-selective hollow fiber thin film composite forward osmosis membrane in osmosis membrane bioreactor (OMBR) system for urban wastewater treatment. CFV of draw solution was optimized, followed by the impact assessment of three CFVs on feed solution (FS) stream and periodic injection of air scouring into the side-stream module. Overall, the OMBR system exhibited high and stable performance with initial water flux of approximately 15 LMH, high removal efficiencies of bulk organic matter and nutrients. While FS's CFVs insignificantly affected the performance and membrane fouling, regular air scouring showed substantial impact with better performance and high efficiency in mitigating membrane fouling. These results indicated that periodic air scouring can be applied into the side-stream membrane module for efficient fouling mitigation without interruption the operation of the OMBR system.

Simultaneous nitrification-denitrification using baffled osmotic membrane bioreactor-microfiltration hybrid system at different oxic-anoxic conditions for wastewater treatment.

The efficacy of a baffled osmotic membrane bioreactor-microfiltration (OMBR-MF) hybrid system equipped with thin film forward osmosis membrane for wastewater treatment was evaluated at laboratory scale. The novel OMBR-MF hybrid system involved baffles, that separate oxic and anoxic zones in the aerobic reactor for simultaneous nitrification and denitrification (SND), and a bioreactor comprised of thin film composite-forward osmosis (TFC-FO) and polyether sulfone-microfiltration (PES-MF) membranes. The evaluation was conducted under four different oxic-anoxic cycle patterns. Changes in flux, salinity build-up, and microbial activity (e.g., extracellular polymeric substances (EPS) were assessed. Over the course of a 34 d test, the OMBR-MF hybrid system achieved high removal of total organic carbon (TOC) (86-92%), total nitrogen (TN) (63-76%), and PO4-P (57-63%). The oxic-anoxic cycle time of 0.5-1.5 h was identified to be the best operating condition. Incorporation of MF membrane effectively alleviated salinity build-up in the reactor, allowing stable system operation.

Energy efficient 3D printed column type feed spacer for membrane filtration.

Modification of the feed spacer design significantly influences the energy consumption of membrane filtration processes. This study developed a novel column type feed spacer with the aim to reduce the specific energy consumption (SEC) of the membrane based water filtration system. The proposed spacer increases the clearance between the filament and the membrane (reducing the spacer filament diameter) while keeping the same flow channel thickness as compared to a standard non-woven symmetric spacer. Since the higher clearance reduces the flow unsteadiness, column type nodes were added in the spacer structure as additional vortex shading bodies. Fluid flow behaviour in the channel for this spacer was numerically simulated by 3D CFD studies and then compared with the standard spacer. The numerical results showed that the proposed spacer substantially reduced the pressure drop, shear stress at the constriction region and shortened the dead zone. Finally, these findings were confirmed experimentally by investigating the filtration performances using the 3D printed prototypes of these spacers in a lab-scale filtration module. It is observed that the column spacer reduced the pressure drop by three times and doubled the specific water flux. 2D OCT (Optical Coherence Tomography) scans of the membrane surface acquired after the filtration revealed much lower biomass accumulation using the proposed spacer. Consequently, the SEC for the column spacer was found about two folds lower than the standard spacer.

Human urine as a forward osmosis draw solution for the application of microalgae dewatering.

Human urine is a unique solution that has the right composition to constitute both a severe environmental threat and a rich source of nitrogen and phosphorous. In fact, between 4-9% of urine mass consists of ions, such as K+, Cl-, Na+ or NH4+. Because of its high ionic strength, urine osmotic pressure can reach values of up to 2000 kPa. With this in mind, this work aimed to study the effectiveness of real urine as a novel draw solution for forward osmosis. Water flux, reverse nitrogen flux and membrane fouling were investigated using fresh or hydrolysed urine. Water flux as high as 16.7 ± 1.1 L m-2 h-1 was recorded using real hydrolysed urine. Additionally, no support layer membrane fouling was noticed in over 20 h of experimentation. Urine was also employed to dewater a Chlorella vulgaris culture. A fourfold increase in algal concentration was achieved while having an average flux of 14.1 L m-2 h-1. During the algae dewatering, a flux decrease of about 19% was noticed; this was mainly due to a thin layer of algal deposition on the active side of the membrane. Overall, human urine was found to be an effective draw solution for forward osmosis.

Understanding the organic micropollutants transport mechanisms in the fertilizer-drawn forward osmosis process.

We systematically investigated the transport mechanisms of organic micropollutants (OMPs) in a fertilizer-drawn forward osmosis (FDFO) membrane process. Four representative OMPs, i.e., atenolol, atrazine, primidone, and caffeine, were chosen for their different molecular weights and structural characteristics. All the FDFO experiments were conducted with the membrane active layer on the feed solution (FS) side using three different fertilizer draw solutions (DS): potassium chloride (KCl), monoammonium phosphate (MAP), and diammonium phosphate (DAP) due to their different properties (i.e., osmotic pressure, diffusivity, viscosity and solution pH). Using KCl as the DS resulted in both the highest water flux and the highest reverse solute flux (RSF), while MAP and DAP resulted in similar water fluxes with varying RSF. The pH of the FS increased with DAP as the DS due to the reverse diffusion of NH4+ ions from the DS toward the FS, while for MAP and DAP DS, the pH of the FS was not impacted. The OMPs transport behavior (OMPs flux) was evaluated and compared with a simulated OMPs flux obtained via the pore-hindrance transport model to identify the effects of the OMPs structural properties. When MAP was used as DS, the OMPs flux was dominantly influenced by the physicochemical properties (i.e., hydrophobicity and surface charge). Those OMPs with positive charge and more hydrophobic, exhibited higher forward OMP fluxes. With DAP as the DS, the more hydrated FO membrane (caused by increased pH) as well as the enhanced RSF hindered OMPs transport through the FO membrane. With KCl as DS, the structural properties of the OMPs were dominant factors in the OMPs flux, however the higher RSF of the KCl draw solute may likely hamper the OMPs transport through the membrane especially those with higher MW (e.g., atenolol). The pore-hindrance model can be instrumental in understanding the effects of the hydrodynamic properties and the surface properties on the OMPs transport behaviors.

Bromide and iodide selectivity in membrane capacitive deionisation, and its potential application to reduce the formation of disinfection by-products in water treatment.

The formation of toxic disinfection by-products during water disinfection due to the presence of bromide and iodide is a major concern. Current treatment technologies such as membrane, adsorption and electrochemical processes have been known to have limitations such as high energy demand and excessive chemical use. In this study, the selectivity between bromide and iodide, and their removal in membrane capacitive deionisation (MCDI) was evaluated. The results showed that iodide was more selectively removed over bromide from several binary feed waters containing bromide and iodide under various initial concentrations and applied voltages. Even in the presence of significant background concentration of sodium chloride, definite selectivity of iodide over bromide was observed. The high partial-charge transfer coefficient of iodide compared to bromide could be a feasible explanation for high iodide selectivity since both bromide and iodide have similar ionic charge and hydrated radius. The result also shows that MCDI can be a potential alternative for the removal of bromide and iodide during water treatment.

Efficient fouling control using outer-selective hollow fiber thin-film composite membranes for osmotic membrane bioreactor applications.

This paper investigates the efficiency of fouling mitigation methods using a novel outer selective hollow fiber thin-film composite forward osmosis (OSHF TFC FO) membrane for osmosis membrane bioreactor (OMBR) system treating municipal wastewater. Two home-made membrane modules having similar transport properties were used. Two operation regimes with three different fouling mitigation strategies were utilized to test the easiness of membrane for fouling cleaning. These two membrane modules demonstrated high performance with high initial water flux of 14.4 LMH and 14.1 LMH and slow increase rate of mixed liquor's salinity in the bioreactor using 30 g/L NaCl as draw solution. OMBR system showed high removals of total organic carbon and NH4 + -N (>98%). High fouling cleaning efficiency was achieved using OSHF TFC FO membrane with different fouling control methods. These results showed that this membrane is suitable for OMBR applications due to its high performance and its simplicity for fouling mitigation.

Techno-economic feasibility of recovering phosphorus, nitrogen and water from dilute human urine via forward osmosis.

Due to high phosphorus (P) and nitrogen (N) content, human urine has often proven to suitable raw material for fertiliser production. However, most of the urine diverting toilets or male urinals dilute the urine 2 to 10 times. This decreases the efficiency in the precipitation of P and stripping of N. In this work, a commercial fertiliser blend was used as forward osmosis (FO) draw solution (DS) to concentrate real diluted urine. During the concentration, the urea in the urine is recovered as it diffuses to the fertiliser. Additionally, the combination of concentrate PO43-, reverse Mg2+ flux from the DS and the Mg2+ presents in the flushing water, was able to recover the PO43- as struvite. With 50% concentrated urine, 93% P recovery was achieved without the addition of an external Mg2+. Concurrently, 50% of the N was recovered in the diluted fertiliser DS. An economic analysis was performed to understand the feasibility of this process. It was found that the revenue from the produced fertilisers could potentially offset the operational and capital costs of the system. Additionally, if the reduction in the downstream nutrients load is accounted for, the total revenue of the process would be over 5.3 times of the associated costs.

Fabricating robust thin film composite membranes reinforced on woven mesh backing fabric support for pressure assisted and forward osmosis: A dataset.

The data presented in this paper are produced as part of the original research article entitled "Thin-film composite membrane on a compacted woven backing fabric for pressure assisted osmosis" (Sahebi et al., 2017). This article describes how to fabricate a defect free membrane for forward osmosis (FO) and pressure assisted osmosis (PAO) on the woven mesh backing fabric support. Casting polymer on backing fabric support may limit the interfacial polyemirization due to wrinkled membrane surface. This paper presents data obtained from two different backing fabrics used as support for fabrication of thin film composite FO membrane. Backing fabric support were woven polyester mesh with different opening size. The data include the characterization of the intrinsic properties of the membrane samples, SEM and their performance under FO process. The structural parameters (S value) of the substrate were computed from thickness and porosity of the substrates. Thin film composite (TFC) membrane achieved a water flux of 8.1 L m2 h-1 in FO process and 37 L m2 h-1 using 0.5 M NaCl as draw solution (DS) and deionised (DI) water as the feed solution (FS) when applied hydraulic pressure was 10 bar.

Forward osmosis system analysis for optimum design and operating conditions.

Low energy consumption and less fouling propensity of forward osmosis (FO) processes have been attractive as a promising water filtration technology. The performance of this process is however significantly influenced by its operating conditions. Moreover, these operating parameters have both favourable and adverse effects on its performance. Therefore, it is very important to optimize its performance for efficient and economic operation. This study aims to develop a software to analyze a full-scale FO system for optimum performance. A comprehensive theoretical framework was developed to estimate the performance of FO system. Analysis results were compared with the experimental results to validate the models. About 5% deviation of simulation results and the experimental findings shows a very good agreement between them. A novel optimization algorithm was then developed to estimate the minimum required draw solution (DS) inlet flowrate and the number of elements in a pressure vessel to attain the design objectives (i.e. desired final DS concentration and recovery rate at a specific feed solution (FS) flowrate). A detailed parametric study was also conducted to determine the optimum operating conditions for different objectives. It showed that for a specific design objective, higher recovery rate can be achieved by increasing the DS flowrate and number of elements in a pressure vessel. In contrast, lower final concentration can be obtained by lowering the DS flowrate and increasing the number of elements. Finally, a MATLAB based software with graphical user interface was developed to make the analysis process easier and efficient.

Modification of Nanofiber Support Layer for Thin Film Composite forward Osmosis Membranes via Layer-by-Layer Polyelectrolyte Deposition.

Electrospun nanofiber-supported thin film composite membranes are among the most promising membranes for seawater desalination via forward osmosis. In this study, a high-performance electrospun polyvinylidenefluoride (PVDF) nanofiber-supported thin film composite (TFC) membrane was successfully fabricated after molecular layer-by-layer polyelectrolyte deposition. Negatively-charged electrospun polyacrylic acid (PAA) nanofibers were deposited on electrospun PVDF nanofibers to form a support layer consisted of PVDF and PAA nanofibers. This resulted to a more hydrophilic support compared to the plain PVDF nanofiber support. The PVDF-PAA nanofiber support then underwent a layer-by-layer deposition of polyethylenimine (PEI) and PAA to form a polyelectrolyte layer on the nanofiber surface prior to interfacial polymerization, which forms the selective polyamide layer of TFC membranes. The resultant PVDF-LbL TFC membrane exhibited enhanced hydrophilicity and porosity, without sacrificing mechanical strength. As a result, it showed high pure water permeability and low structural parameter values of 4.12 L m-2 h-1 bar-1 and 221 µm, respectively, significantly better compared to commercial FO membrane. Layer-by-layer deposition of polyelectrolyte is therefore a useful and practical modification method for fabrication of high performance nanofiber-supported TFC membrane.