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.

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.

Removal behaviors and fouling mechanisms of charged antibiotics and nanoparticles on forward osmosis membrane.

Fouling and rejection mechanisms of both charged antibiotics (ABs) and nanoparticles (NPs) were determined using a negatively-charged polyamide thin film composite forward osmosis (FO) flat sheet membrane. Two types of ABs and NPs were selected as positively and negatively charged foulants at pH 8. The ABs did not cause significant membrane fouling, but the extent of fouling and rejection changed based on the electrostatic attraction or repulsion forces. The addition of opposite charged AB and NP resulted in a decline of the membrane flux by 11.0% but a 6.5% AB average rejection efficiency improvement. On the other hand, mixing of like-charged ABs and NPs generated repulsive forces that improved average rejection efficiency about 5.5% but made no changes in the membrane flux. In addition, NPs and ABs were mixed and tested at various concentrations and pH levels to rectify the behavior of ABs. The aggregate size and removal efficiency were observed to vary with the change in the electron double layer of the mixture. It can help to make the strategy to control the ABs in the FO process and consequently it enables the FO process to produce environmentally safe effluent.

Volatile fatty acids and biogas recovery using thermophilic anaerobic membrane distillation bioreactor for wastewater reclamation.

The effects of bioreactor temperatures and salinities of an anaerobic membrane distillation bioreactor (anMDBR) on the permeation performance and their potential recovery of bioresources were fully examined in this study. To the best of our knowledge, this is the first study of a lab-scale anMDBR process utilizing sub-merged hollow fiber membranes. The hybrid system utilizing both membrane distillation (MD) and anaerobic bioreactors achieved 99.99% inorganic salt rejection regardless the operation temperatures and high initial flux from (2-4 L m-2 h-1) at 45-65 °C. However, after 7-day operation, the flux dropped by 16-50% proportional to the bioreactor temperatures. It was found that the effects of bioreactor temperatures had strong impacts on both the permeation performance and fouling behavior while salinity had insignificant effect. A compact non-porous fouling layer was observed on the membrane surface from the bioreactor operated at 65 °C while only a few depositions was found on the membrane from 45 °C bioreactor. In the present study, the optimal anMDBR temperature was found to be 45 °C, showing a balanced biogas production and membrane permeation performance including less fouling formation. At this bioreactor temperature (45 °C), the biogas yield was 0.14 L/g CODremoval, while maintaining a methane recovery of 42% in the biogas, similar recovery to those at bioreactor temperatures of 55 and 65 °C. The potential recovery of volatile fatty acids made anMDBR a more economically efficient system, in addition to its lower operation cost and smaller footprint compared with most other technologies for on-site wastewater treatment.

Removal of fluoride in membrane-based water and wastewater treatment technologies: Performance review.

The presence of excess fluoride in aqueous media above local environmental standards (e.g., the U.S. Environmental Protection Agency (EPA) standard of 4 mg/L) affects the health of aquatic life. Excess fluoride in drinking water above the maximum contaminant level (e.g., the World Health Organization (WHO) standard of 1.5 mg/L) also affects the skeletal and nervous systems of humans. Fluoride removal from aqueous solutions is difficult using conventional electrochemical, precipitation, and adsorption methods owing to its ionic size and reactivity. Thus, new technologies have been introduced to reduce the fluoride concentration in industrial wastewater effluents and various drinking water sources. Membrane technology is one of the newer technologies found to be very effective in significantly reducing fluoride to desired standards levels; however, it has received less attention than other technologies because it is perceived as a costly process. This study critically reviewed the performance of various membrane process and compared it with effluent and zero liquid discharge (ZLD) standards. The performance review has been conducted with the consideration of the theoretical background, rejection mechanisms, technical viability, and parameters affecting flux and rejection performance. This review includes membrane systems investigated for the defluoridation process but operated under pressure (i.e., reverse osmosis [RO] and nanofiltration [NF]), temperature gradients (i.e., membrane distillation [MD]), electrical potential gradients (i.e., electrodialysis [ED] and Donnan dialysis [DD]), and concentration differences (i.e., forward osmosis [FO]). Moreover, the study also addressed the advantages, limitations, & applicable conditions of each membrane based defluoridation process.

Hierarchical Composite Membranes with Robust Omniphobic Surface Using Layer-By-Layer Assembly Technique.

In this study, composite membranes were fabricated via layer-by-layer (LBL) assembly of negatively charged silica aerogel (SiA) and 1H,1H,2H,2H-perfluorodecyltriethoxysilane (FTCS) on a polyvinylidene fluoride phase inversion membrane and interconnecting them with positively charged poly(diallyldimethylammonium chloride) (PDDA) via electrostatic interaction. The results showed that the PDDA-SiA-FTCS coated membrane had significantly enhanced the membrane structure and properties. New trifluoromethyl and tetrafluoroethylene bonds appeared at the surface of the coated membrane, which led to lower surface free energy of the composite membrane. Additionally, the LBL membrane showed increased surface roughness. The improved structure and property gave the LBL membrane an omniphobic property, as indicated by its good wetting resistance. The membrane performed a stable air gap membrane distillation (AGMD) flux of 11.22 L/m2 h with very high salt rejection using reverse osmosis brine from coal seam gas produced water as feed with the addition of up to 0.5 mM SDS solution. This performance was much better compared to those of the neat membrane. The present study suggests that the enhanced membrane properties with good omniphobicity via LBL assembly make the porous membranes suitable for long-term AGMD operation with stable permeation flux when treating challenging saline wastewater containing low surface tension organic contaminants.

Combining high performance fertiliser with surfactants to reduce the reverse solute flux in the fertiliser drawn forward osmosis process.

Solutions to mitigate the reverse diffusion of solutes are critical to the successful commercialisation of the fertiliser drawn forward osmosis process. In this study, we proposed to combine a high performance fertiliser (i.e., ammonium sulfate or SOA) with surfactants as additives as an approach to reduce the reverse diffusion of ammonium ions. Results showed that combining SOA with both anionic and non-ionic surfactants can help in reducing the reverse salt diffusion by up to 67%. We hypothesised that, hydrophobic interactions between the surfactant tails and the membrane surface likely constricted membrane pores resulting in increased rejection of ions with large hydrated radii such as SO42-. By electroneutrality, the rejection of the counter ions (i.e., NH4+) also therefore subsequently improved. Anionic surfactant was found to further decrease the reverse salt diffusion due to electrostatic repulsions between the surfactant negatively-charged heads and SO42-. However, when the feed solution contains cations with small hydrated radii (e.g., Na+); it was found that NH4+ ions can be substituted in the DS to maintain its electroneutrality and thus the diffusion of NH4+ to the feed solution was increased.

Computing the effective diffusion coefficient of solutes in a multi-salts solutions during forward osmosis (FO) membrane filtration: Experiments and mathematical modelling.

Diffusion coefficient of solutes through a porous membrane media is different from diffusion coefficient through a free homogenous media. Porosity, tortuosity and the thickness of the membrane significantly affect the diffusion through a specific thickness of a membrane and therefore it is termed as effective diffusion coefficient (Deff) which is lower than the actual diffusion coefficient, D. The Deff of single or dual solutes through a porous membrane layer are well documented but not for multiple salts. Therefore, in this study, single, dual and multiple salt mixtures were passed through a flat sheet cellulose triacetate Forward Osmosis (FO) membrane to obtain a semi-empirical relationship with the Deff and its water flux. This will allow computing the structural coefficient of FO membranes. Research community have spent tremendous efforts in membrane modification to reduce the structural coefficient to improve FO process efficiency. Our finding suggests that optimising the draw solution chemistry can achieve this goal.

Engineering the Re-Entrant Hierarchy and Surface Energy of PDMS-PVDF Membrane for Membrane Distillation Using a Facile and Benign Microsphere Coating.

To consolidate the position of membrane distillation (MD) as an emerging membrane technology that meets global water challenges, it is crucial to develop membranes with ideal material properties. This study reports a facile approach for a polyvinylidene fluoride (PVDF) membrane surface modification that is achieved through the coating of the surface with poly(dimethylsiloxane) (PDMS) polymeric microspheres to lower the membrane surface energy. The hierarchical surface of the microspheres was built without any assistance of a nano/microcomposite by combining the rapid evaporation of tetrahydrofuran (THF) and the phase separation from condensed water vapor. The fabricated membrane exhibited superhydrophobicity-a high contact angle of 156.9° and a low contact-angle hysteresis of 11.3°-and a high wetting resistance to seawater containing sodium dodecyl sulfate (SDS). Compared with the control PVDF-hexafluoropropylene (HFP) single-layer nanofiber membrane, the proposed fabricated membrane with the polymeric microsphere layer showed a smaller pore size and higher liquid entry pressure (LEP). When it was tested for the direct-contact MD (DCMD) in terms of the desalination of seawater (3.5% of NaCl) containing SDS of a progressively increased concentration, the fabricated membrane showed stable desalination and partial wetting for the 0.1 and 0.2 mM SDS, respectively.

Evaluation of fertilizer-drawn forward osmosis for sustainable agriculture and water reuse in arid regions.

The present study focused on the performance of the FDFO process to achieve simultaneous water reuse from wastewater and production of nutrient solution for hydroponic application. Bio-methane potential (BMP) measurements were firstly carried out to determine the effect of osmotic concentration of wastewater achieved in the FDFO process on the anaerobic activity. Results showed that 95% water recovery from the FDFO process is the optimum value for further AnMBR treatment. Nine different fertilizers were then tested based on their FO performance (i.e. water flux, water recovery and reverse salt flux) and final nutrient concentration. From this initial screening, ammonium phosphate monobasic (MAP), ammonium sulfate (SOA) and mono-potassium phosphate were selected for long term experiments to investigate the maximum water recovery achievable. After the experiments, hydraulic membrane cleaning was performed to assess the water flux recovery. SOA showed the highest water recovery rate, up to 76% while KH2PO4 showed the highest water flux recovery, up to 75% and finally MAP showed the lowest final nutrient concentration. However, substantial dilution was still necessary to comply with the standards for fertigation even if the recovery rate was increased.

Fatty acid fouling of forward osmosis membrane: Effects of pH, calcium, membrane orientation, initial permeate flux and foulant composition.

Octanoic acid (OA) was selected to represent fatty acids in effluent organic matter (EOM). The effects of feed solution (FS) properties, membrane orientation and initial permeate flux on OA fouling in forward osmosis (FO) were investigated. The undissociated OA formed a cake layer quickly and caused the water flux to decline significantly in the initial 0.5hr at unadjusted pH3.56; while the fully dissociated OA behaved as an anionic surfactant and promoted the water permeation at an elevated pH of 9.00. Moreover, except at the initial stage, the sudden decline of water flux (meaning the occurrence of severe membrane fouling) occurred in two conditions: 1. 0.5mmol/L Ca(2+), active layer facing draw solution (AL-DS) and 1.5mol/L NaCl (DS); 2. No Ca(2+), active layer-facing FS (AL-FS) and 4mol/L NaCl (DS). This demonstrated that cake layer compaction or pore blocking occurred only when enough foulants were absorbed into the membrane surface, and the water permeation was high enough to compact the deposit inside the porous substrate. Furthermore, bovine serum albumin (BSA) was selected as a co-foulant. The water flux of both co-foulants was between the fluxes obtained separately for the two foulants at pH3.56, and larger than the two values at pH9.00. This manifested that, at pH3.56, BSA alleviated the effect of the cake layer caused by OA, and OA enhanced BSA fouling simultaneously; while at pH9.00, the mutual effects of OA and BSA eased the membrane fouling.

Rare earth europium recovery using selective metal-organic framework incorporated mixed-matrix membrane.

Rare-earth elements (REEs) play a crucial role in state-of-the-art technologies and sustainable energy generation. However, conventional production methods of REE often instigate detrimental impacts on environment. Hence, the development of efficient and sustainable hydrometallurgical methods for REE recovery from complex solution has become a crucial research focus. This study investigates a mixed-matrix membrane composed of a highly europium selective metal-organic framework-based adsorbent, Cr-MIL-PMIDA, embedded in sulfonated poly(ether ketone) (SPEK) polymer membrane matrix to preferentially concentrate europium (Eu3+) ions in the presence of other competing cations. The activated membrane notably reduced ionic conductivity for Eu3+ compared to other multivalent ions. Membrane extraction experiments further confirmed the selective behavior, demonstrating slower diffusion for Eu3+ compared to Mg2+ and Zn2+ cations. Especially, at pH 5, Mg2⁺ and Zn2⁺ recovery was greater than 30%, whereas Eu³âº recovery remained lower than 4%. We propose that the strong chemical affinity between the phosphate group and Eu3+ help partition of the Eu3+ ions in the membrane phase and inhibit the diffusion and further partitioning of the Eu3+ ion from bulk solution. Furthermore, we demonstrate the stability of the composite membrane and the embedded MOF particles in aqueous solution for up to 12 days without degradation, attributing it to the robust chemical stability of the MOF structure.

Machine learning for layer-by-layer nanofiltration membrane performance prediction and polymer candidate exploration.

In this study, machine learning-based models were established for layer-by-layer (LBL) nanofiltration (NF) membrane performance prediction and polymer candidate exploration. Four different models, i.e., linear, random forest (RF), boosted tree (BT), and eXtreme Gradient Boosting (XGBoost), were formed, and membrane performance prediction was determined in terms of membrane permeability and selectivity. The XGBoost exhibited optimal prediction accuracy for membrane permeability (coefficient of determination (R2): 0.99) and membrane selectivity (R2: 0.80). The Shapley Additive exPlanation (SHAP) method was utilized to evaluate the effects of different LBL NF membrane fabrication conditions on membrane performances. The SHAP method was also used to identify the relationships between polymer structure and membrane performance. Polymers were represented by Morgan fingerprint, which is an effective description approach for developing modeling. Based on the SHAP value results, two reference Morgan fingerprints were constructed containing atomic groups with positive contributions to membrane permeability and selectivity. According to the reference Morgan fingerprint, 204 potential polymers were explored from the largest polymer database (PoLyInfo). By calculating the similarities between each potential polymer and both reference Morgan fingerprints, 23 polymer candidates were selected and could be further used for LBL NF membrane fabrication with the potential for providing good membrane performance. Overall, this work provided new ways both for LBL NF membrane performance prediction and high-performance polymer candidate exploration. The source code for the models and algorithms used in this study is publicly available to facilitate replication and further research. https://github.com/wangliwfsd/LLNMPP/.

Electrically conductive membrane distillation via an alternating current operation for zero liquid discharge.

Membrane distillation (MD) shows promise for achieving high salinity treatment and zero liquid discharge (ZLD) compared to conventional water treatment processes due to its unique characteristics, including low energy consumption and high resulting water quality. However, performance degradation due to fouling and scaling under high recovery conditions remains a challenge, particularly considering the need to control both cations and anions for maximum scaling mitigation. Accordingly, in this study, alternating current (AC) operation for electrically conductive membrane distillation (ECMD) is newly proposed, based on its potential for controlling both cations and anions, in contrast to conventional direct current (DC) operation. Systematic experiments and theoretical analysis show that water recovery in ECMD can be increased by 27% through AC operation. The proposed modification and effective AC operation of ECMD increase the practicality of using MD in desalination for a high recovery rate, perhaps even for ZLD.

Electrospun nanofiber composite membranes for geothermal brine treatment with lithium enrichment via membrane distillation.

In this study, a composite electrospun nanofiber membrane was fabricated and used to treat a geothermal brine source with lithium enrichment. An in-situ growth technique was applied to incorporate silica nanoparticles on the surface of nanofibers with (3-Aminopropyl) triethoxysilane as the nucleation site. The fabricated composite nanofiber membrane was heat pressed to enhance the integration of the membrane and its mechanical stability. The fabricated membranes were tested to evaluate their performance in feedwater containing different concentrations of NaCl in the range of 0-100 g/L, and the wetting resistivity of the membranes was examined. Finally, the optimal membrane was applied to treat the simulated geothermal brine. The experimental results revealed that the in-situ growth of nanoparticles and coating of flourosilane agent dramatically improved the separation performance of the membrane with high salt rejection, and adequate flux was achieved. The heat-pressed membrane obtained >99% salt rejection and flux of 14-19 L/m2h at varying feedwater salinity (0-100 g/L), and the concentration of the Li during the 24 h test reached >1100 ppm from the initial 360 ppm. Evaluation of the energy efficiency of the membranes showed that the heat-pressed membrane obtained the optimum energy efficiency in the high concentration of salts. Additionally, the economic analysis indicated that MD could achieve a levelized cost of 2.9 USD/m3 of lithium brine concentration as the heat source is within the feed. Overall, this technology would represent a viable alternative to the solar pond to concentrate Li brine, enabling a compact, efficient, and continuous operating system.

Computational fluid dynamics simulation study of hypersaline water desalination via membrane distillation: Effect of membrane characteristics and operational parameters.

In this study, a comprehensive model was developed using Computational Fluid Dynamics (CFD), and the behaviour of a direct contact membrane distillation (DCMD) system was investigated at hypersaline feedwater conditions. The effects of various operating parameters including feed and permeate velocities, temperatures and salinities, as well as different membrane characteristics like thickness, porosity, and thermal conductivity were studied. The developed simulation model was also validated using experimental data. The results showed that the membrane conductivity and thickness had a significant impact on the DCMD performance, and the optimum operational condition was necessary to be determined. The results showed that increasing the feedwater salinity from 50 to 200 g/l decreased the membrane flux by up to 33%, while a four times decrease in thermal conductivity of the membrane could lead to an increase in the membrane flux from 11.2 to 32.4 l/m2·h (LMH). In addition, the optimal membrane thickness was found to increase with salinity, reaching >120 µm for treatment of 22 wt% NaCl feedwater solution. However, the flux declined from >32 LMH to <13 LMH upon the increase in feedwater salinity (up to 22 wt% NaCl solution). It is also shown that a thinner membrane performed better for desalination of low salinity feedwater, while the thicker one produces higher separation performance and thermal efficiency for hypersaline brine desalination.

Highly stable gold nanolayer membrane for efficient solar water evaporation under a harsh environment.

Interfacial solar water evaporation has attracted tremendous attention for sunlight harvesting for water purification. However, salt formation and stability of the photothermal materials (PTMs) remain a challenge that need addressing before bringing this technology to real-world applications. In this work, a nanoscale thin film of gold (Au) on a polytetrafluoroethylene (PTFE) membrane has been prepared using a magnetic sputtering technique. The fabricated membrane displays a robust mechanical strength and chemical stability arising from the adhesiveness of the thin film Au nanolayer on the PTFE membrane as well as the chemical inertness of the noble metal PTM. The Au nanolayer/PTFE membrane with cellulose sponge substrate resulted in an evaporation rate of 0.88 kg m-2 h-1 under 1 sun intensity. Remarkable salt ion rejection of 99.9% has been obtained, meeting the required standard for drinking water. Moreover, the membrane exhibited excellent stability and reusability in natural seawater and high salinity brine (150 g/L) and even in severe conditions (acidic, basic, and oxidized). No noticeable salt formation was observed on the evaporator surface after the tests. These findings reveal promising prospects for using a magnetron sputtering technique to fabricate a stable photothermal membrane for seawater and high salinity brine desalination.

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.

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.

Forward osmosis with direct contact membrane distillation using tetrabutylphosphonium p-toluenesulfonate as an effective and safe thermo-recyclable osmotic agent for seawater desalination.

A phosphonium-based ionic liquid (IL) with lower critical solution temperature (LCST) property was assessed as a reusable draw solution (DS) for forward osmosis (FO). Tetrabutylphosphonium p-toluenesulfonate ([P4444]TsO) was successfully synthesized by neutralization reaction. Characterization results reveal its ability to generate sufficient osmotic pressure (14-68 bars for 0.5-2 M DS) to create a gradient across the FO membrane. Its thermal, physico-chemical and other colligative properties are favorable for its application as an osmotic agent. The LCST behavior of [P4444]TsO was found reversible and its phase separation from water can be done above its cloud point temperature Tc ∼57 °C. In vitro cytotoxicity tests from LDH and MTT assay reveal that it can be safely used as DS at an effective concentration EC30 ∼57 mg L-1 as its non-toxic level. Results from FO operations demonstrate that 2 M [P4444]TsO DS can effectively treat saline feed like seawater (0.6 M NaCl) with reasonable Jv = 1.35 ± 0.15 L m-2h-1, low Js = 0.0038 ± 0.00049 mol m-2h-1, and considerably low specific solute flux (Js/Jv âˆ¼ 0.0028 mol L-1). After FO, ∼98% of [P4444]TsO was precipitated by heating the DS at 60 °C and conveniently reused with consistent FO performance. Direct contact membrane distillation (DCMD) was found effective in removing the residual 2% [P4444]TsO in the DS supernatant to finally produce high-quality effluent with concentrations way below the EC30 limit. Cost estimates for the entire process reveal the potential of FO combined with thermo-cyclic [P4444]TsO regeneration with DCMD for desalination application.