An efficient data-driven desalination approach for the element-scale forward osmosis (FO)-reverse osmosis (RO) hybrid systems.

Freshwater shortages are a consequence of the rapid increase in population, and desalination of saltwater has gained popularity as an alternative water treatment method in recent years. To date, the forward osmosis-reverse osmosis (FO-RO) hybrid technology has been proposed as a low-energy and environmentally friendly next-generation seawater desalination process. Scaling up the FO-RO hybrid system significantly affects the success of a commercial-scale process. However, neither the ideal structure nor the membrane components for plate-and-frame FO (PFFO) and spiral-wound FO (SWFO) are known. This study aims to explore and optimize the performance of SWFO-RO and PFFO-RO hybrid element-scale systems in the desalination of seawater. The results showed that both hybrid systems could yield high water recovery under optimal operating conditions. The prediction of the system performance (water flux and reverse salt flux) by artificial intelligence was considerably better (R > 0.99, root mean square error <5%) than that of conventional mass balance models. A Markov-based decision tree successfully classified the water flux level in hybrid systems. An optimal set of operational conditions for each membrane system was proposed. For example, in RO, a combination of the feed solution (FS) flow rate (≥17.5 L/min), FS concentration (<17,500 ppm), and operation pressure (<35 bar) would result in high water permeability (>40 LMH). In addition, five SWFO elements and four PFFO elements should be the optimal numbers of FO membranes in the hybrid FO-RO system for effective seawater desalination, especially for long-term operation.

Simple and Low-Cost Electroactive Membranes for Ammonia Recovery.

Ammonia is considered a contaminant to be removed from wastewater. However, ammonia is a valuable commodity chemical used as the primary feedstock for fertilizer manufacturing. Here we describe a simple and low-cost ammonia gas stripping membrane capable of recovering ammonia from wastewater. The material is composed of an electrically conducting porous carbon cloth coupled to a porous hydrophobic polypropylene support, that together form an electrically conductive membrane (ECM). When a cathodic potential is applied to the ECM surface, hydroxide ions are produced at the water-ECM interface, which transforms ammonium ions into higher-volatility ammonia that is stripped across the hydrophobic membrane material using an acid-stripping solution. The simple structure, low cost, and easy fabrication process make the ECM an attractive material for ammonia recovery from dilute aqueous streams, such as wastewater. When paired with an anode and immersed into a reactor containing synthetic wastewater (with an acid-stripping solution providing the driving force for ammonia transport), the ECM achieved an ammonia flux of 141.3 ± 14.0 g.cm-2.day-1 at a current density of 6.25 mA.cm-2 (69.2 ± 5.3 kg(NH3-N)/kWh). It was found that the ammonia flux was sensitive to the current density and acid circulation rate.

High-Efficiency Recovery of Acetic Acid from Water Using Electroactive Gas-Stripping Membranes.

Recovery of carbon-based resources from waste is a critical need for achieving carbon neutrality and reducing fossil carbon extraction. We demonstrate a new approach for extracting volatile fatty acids (VFAs) using a multifunctional direct heated and pH swing membrane contactor. The membrane is a multilayer laminate composed of a carbon fiber (CF) bound to a hydrophobic membrane and sealed with a layer of polydimethylsiloxane (PDMS); this CF is used as a resistive heater to provide a thermal driving force for PDMS that, while a highly hydrophobic material, is known for its ability to rapidly pass gases, including water vapor. The transport mechanism for gas transport involves the diffusion of molecules through the free volume of the polymer matrix. CF coated with polyaniline (PANI) is used as an anode to induce an acidic pH swing at the interface between the membrane and water, which can protonate the VFA molecule. The innovative multilayer membrane used in this study has successfully demonstrated a highly efficient recovery of VFAs by simultaneously combining pH swing and joule heating. This novel technique has revealed a new concept in the field of VFA recovery, offering promising prospects for further advancements in this area. The energy consumption was 3.37 kWh/kg for acetic acid (AA), and an excellent separation factor of AA/water of 51.55 ± 2.11 was obtained with high AA fluxes of 51.00 ± 0.82 g.m-2hr-1. The interfacial electrochemical reactions enable the extraction of VFAs without the need for bulk temperature and pH modification.

Ionic fluid as a novel cleaning agent for the control of irreversible fouling in reverse osmosis membrane processes.

While a variety of chemical cleaning strategies has been studied to control fouling in membrane-based water treatment processes, the removal of irreversible foulants strongly bound on membrane surfaces has not been successful. In this study, we firstly investigated the diluted aqueous solutions of ionic fluid (IF, 1-ethyl-3-methylimidazolium acetate) as a cleaning agent for three model organic foulants (humic acid, HA; bovine serum albumin, BSA; sodium alginate, SA). The real-time monitoring of cleaning progress by optical coherence tomography (OCT) showed that fouling layer was dramatically swelled by introducing IF solution and removed by shear force exerted during cleaning. This phenomenon was induced due to the pre-existing interactions between organic foulants were weakened by the intrusion of IF into the fouling layer, which was analyzed by the measurement of adhesion forces using atomic force microscopy (AFM). In the experiments with model foulants and wastewater effluent, IF was added to alkaline cleaning agents (NaOH) to verify the applicability to be supplemented in commercial cleaning agents, and resulted in the significantly enhanced control of irreversible membrane fouling. Implication of utilizing recyclable IF with negligible volatility is that environmental effects of membrane cleaning solutions could be minimized by decreasing usage of cleaning chemicals, while increasing the cleaning efficiency.

Possibility assessment of ultrafiltration membrane pre-treatment efficiency for brackish water reverse osmosis-based wastewater reuse: Lab and demonstration.

Ultrafiltration (UF) membranes are considered a pre-treatment for brackish water reverse osmosis (BWRO) membranes because of the high rejection rate of particulates and the productivity of the final water quantity. This study presents the performance and membrane surface property analysis of UF membranes for commercial membrane manufacturers, and their structural strength and chemical resistance were evaluated. Moreover, the pilot-scale UF-BWRO process was operated for two months using real wastewater based on the results of this study. Although the overall properties were similar, the poly (ether-sulfone) UF membrane showed higher tensile strength than the polyvinylidene difluoride and polyacrylonitrile UF membranes. The UF membrane showed a high removal rate of particulates (over 90%) but low rejection rate of organic compounds, such as humic acid and sodium alginate (below 30%). After exposure to high concentrations of chemicals, the contact angle of the membranes was reduced by approximately 15% compared to that of the virgin membranes. In addition, despite the exposure to low-and high-concentration chemicals, UF membranes were relatively stable in terms of tensile strength. During the operation period of the pilot-scale UF-RO process, the UF membrane showed a high turbidity removal of over 93%, and the UF-BWRO process presented a high salt rejection of over 92%. The UF membrane showed potential for the pre-treatment of BWRO membranes.

Fate, elimination, and simulation of low-molecular-weight micropollutants in an integrated activated carbon-fertiliser drawn osmotic membrane bioreactor.

This study investigated the behaviour and simulation of low-molecular-weight (low-MW) micropollutants (MPs) in a powdered activated carbon (PAC)-assisted fertiliser-drawn OMBR. 10% increase in water recovery and two times thinner fouling layer were observed in OMBR with addition of 100 mg-PAC/g-MLSS. This amount of PAC also boosted the richness and diversity in microbial community (Chao1 and Shannon index increased 1.5 times). Nearly 100% low-MW MPs were eliminated in PAC-OMBR, while 2-80% was achieved with traditional OMBR. This reduced the pathway of low-MW MPs into diluted fertiliser from 47% to < 1% of the total influent mass. Hydrophilicity played the crucial role in the removal of low-MW MPs, especially acetaminophen and nonylphenol. Neural network was suitable for the simulation of MP behaviour with high accuracy (R = 0.98, RMSE = 4.7%). The findings support safer and cleaner use of the diluted fertiliser and promote a cost-effective tool for real-time analysis of MP behaviour.

Facile Surface Modification of Polyamide Membranes Using UV-Photooxidation Improves Permeability and Reduces Natural Organic Matter Fouling.

A new optimized ultraviolet (UV) technique induced a photooxidation surface modification on thin-film composite (TFC) polyamide (PA) brackish water reverse osmosis (BWRO) membranes that improved membrane performance (i.e., permeability and organic fouling propensity). Commercial PA membranes were irradiated with UV-B light (285 nm), and the changes in the membrane performance were assessed through dead-end and cross-flow tests. UV-B irradiation at 12 J·cm-2 enhanced the pure water permeability by 34% in the dead-end tests without decreasing the mono- or divalent ion rejections, as compared with the pristine PA membrane, and led to less fouling by natural organic matter in the cross-flow tests. Scanning electron microscopy (SEM), attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, and X-ray photoelectron spectroscopy (XPS) confirmed that UV-B irradiation opened the pore structure and created carboxylic and amine groups on the PA surface, leading to increased membrane surface charge and hydrophilicity. Thus, an optimal UV-B dose appears to modify only a thin layer of the PA membrane surface, which favorably enhances the membrane performance. UV-B did not alter the structure, flux, or salt rejection for cellulose triacetate (CTA)-based membranes. While other membrane surface modifications include oxidants, strong acids, and bases, the UV-B facile treatment is chemical-free, thus reducing chemical wastes, and easy to apply in roll-to-roll fabrication processes of PA membranes. The results also showed that a low UV irradiation dose could be applied to PA or CTA membranes for disinfection or photocatalytic oxidation.

Effects of microplastics on the removal of trace organic compounds during ozonation: Oxidation and adsorption of trace organic compounds and byproducts.

Trace organic compounds (TOrCs) and microplastics (MPs) have been recognized as emerging pollutants that cause severe water pollution related problems due to their non-degradable and bio-accumulative nature. Many studies on oxidation processes such as ozone have been conducted to efficiently remove TOrCs in water treatment. However, there has been a lack of research on the removal efficiency of TOrCs in the oxidation process when they co-exist with MPs and form transformation byproducts (TBPs) during this process. This study evaluates the effects of MPs on TOrC removal during ozonation at various ozone concentrations and based on the mass of MP particles in distilled water. The adsorption of TBPs and TOrCs was also evaluated using the Freundlich and Langmuir isotherm equations. The toxicity of these compounds was evaluated to confirm the risk to aquatic ecosystems. The results show that triclosan (TCS) had the highest absorption capacity amongst the TOrCs and TBPs tested. Polyvinylchloride exhibited the highest adsorption efficiency compared with polyethylene and polyethyleneterephthalate (TCS 0.341 mg/g) due to its high adsorption capacity and hydrophobicity. In the toxicity test, 2,4-dichlorophenol and 4-chloroaniline as TBPs had a relatively higher toxicity to Vibrio fischeri (a marine bacterial species) than Daphnia magna (a freshwater plankton species).

Low-pressure volume retarded osmosis for removal of per- and polyfluoroalkyl substances.

Forward osmosis is an energy efficient process that is capable of recovering high-quality water from secondary wastewater treatment. However, regeneration of the draw solution (DS) is a problem that needs to be addressed. Herein, we developed and optimized a one-step process that does not require additional treatment for the DS. This process, called pressure assisted-volume retarded osmosis (PA-VRO), utilizes naturally occurring pressure with the aid of a small inlet pressure (< 1 bar). Poly(styrenesulfonate) was employed as the DS, for its high solubility in water and large molecular size (∼70,000 Da). Accordingly, real wastewater was employed as the feed solution for 48 h to remove perfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS) through PA-VRO. The rejection rates for PFOA/PFOS and poly(sodium-4-styrenesulfonate) (PSS) were observed to exceed 98%, after 24 h and 99%, after 48 h. Moreover, there were no traceable amounts of PFOA/PFOS in the DS, and hence the detected concentrations of PFOA and PFOS can be attributed to the residuals from the equipment. Therefore, this well-optimized PA-VRO process can be utilized for potable water production from treated wastewater.

An osmotic membrane bioreactor-clarifier system with a deep learning model for simultaneous reduction of salt accumulation and membrane fouling.

This study investigates a novel hybrid configuration of an osmotic membrane bioreactor-clarifier (OMBRC) to achieve the simultaneous reduction of salt accumulation and membrane fouling. Compared with the conventional OMBR, the OMBRC demonstrated 14 times lower conductivity after 40 d of operation, achieving maximum values exceeding 25,000 and 1800 µS/cm, respectively. The average water flux and flux recovery were approximately 3 and 6 times higher in the OMBRC than in the OMBR, respectively. The ammonium, total organic carbon, and total nitrogen removals of the combined system were measured to be 15%, 11% and 7% higher in the hybrid OMBRC process than in the OMBR, respectively. The hybrid process also reduced the foulant layer thickness in this system to only 15 µm compared with 28 µm in the OMBR. An artificial intelligence-based model was successfully developed for long-term prediction, indicating that the advantages afforded by the hybrid OMBRC can be maintained over long periods of operation with 22 times lower conductivity and 5 times higher water flux compared with the OMBR. A longer lifespan of FO membrane is also predicted in the OMBRC compared to that in the OMBR with the replacements are recommended at 100th and 40th day, respectively.

Effects of co-existence of organic matter and microplastics on the rejection of PFCs by forward osmosis membrane.

Perfluorinated chemical (PFC)-based materials have been widely applied in industry. In this study, the influence of PFCs on the physicochemical properties of membranes and that of the co-existence of organic matter and microplastics on the removal rate in the process of forward osmosis (FO) was examined. The water flux, reverse salt flux, and rejection of PFCs were evaluated under w and w/o contaminants. The lowest rejection rates of PFCs in FO membranes were observed to be 92.2% and 90.4% for FO-TFC and PA-Aqua FO membranes, respectively. The main rejection mechanism of the FO membrane is the sieving effect (p-value: PA-TFC-0.015, PA-Aqua-0.002) based on molecular volume, which is more dominant than the electrostatic repulsive force and hydrophobic interaction, the major rejection mechanisms of existing trace contaminants. In addition, we observed that the effects of co-existing pollutants in raw water have an insignificant effect on the rejection of PFCs because of the physical and chemical stability of PFCs. According to the results of this study, using the FO membrane, PFCs can effectively control not only their self-existence but also when contaminants co-exist with them in water bodies.

Electrochemical recovery of H2 and nutrients (N, P) from synthetic source separate urine water.

This study examined an electrochemical method of H2 production and nutrient recovery from synthetic source separated urine (SSU). The efficacy of H2 production was examined through hydrogen recovery experiments (HRE) using Ni foam electrodes. Similarly, nutrient (N and P) recovery was also examined in post-nutrient recovery experiments (NRE) with sacrificial Mg electrodes. To achieve higher nutrient recovery in the post-nutrient recovery process, the most important operating parameters (initial solution pH (pHi) and current density) were optimized. Optimization of NRE revealed that > 90% NH3-N and PO43--P could be recovered at 8 mA cm-2 with a pHi of 6-8. Notable NH3-N and PO43--P reduction were observed at an equimolar Mg2+ dissolution ratio (1:1) of Mg2+:NH4+ and a 1.1:1 ratio of Mg2+:PO43- respectively. However, poor total Kjeldahl nitrogen (TKN) reduction was observed. Thus, we anticipate that direct electrochemical conversion of urea to N2 at the anode followed by H2 generation at the cathode is a more sustainable way to reduce TKN. Batch HRE showed that the initial TKN, 1094 mg L-1 (934 mg L-1 from urea-N and 160 mg L-1 from NH4Cl), was significantly reduced to 360 mg L-1 by Ni-Ni electrolysis, whereas around 53.8 g H2 gas was received from this Ni-Ni electrolysis system with a flow rate of 5-5.8 g mol-1 day-1. Overall, this work produced a 68% reduction in TKN due to electrochemical conversion of urea into H2.

Characterization and control of membrane fouling during dewatering of activated sludge using a thin film composite forward osmosis membrane.

This study investigated the feasibility of applying a thin film composite (TFC) forward osmosis (FO) membrane in the dewatering of activated sludge (AS). Membrane fouling was investigated and controlled to enhance the system's performance. Investigations showed that the TFC FO membrane provided a water flux that was 120 % higher and a concentration factor that was three times higher compared to a cellulose tri-acetate (CTA) membrane. The foulant layer on the TFC membrane surface was mostly irreversible when 1.44 mg-C/cm2 and 0.13 mg-C/cm2 dissolved organic carbon (DOC) were extracted in sodium hydroxide (NaOH) and deionized (DI) water, respectively. The results of principle component analysis (PCA) revealed that among the operating conditions, the amount of aromatic organic compounds (indicated by UV254 values) followed by their hydrophilicity (specific ultraviolet absorbance (SUVA) indices) were the dominant factors controlling the different fouling potentials. SUVA value indices ranged from 0.4 to 0.6 L/m-mg DOC, illustrating that hydrophilic compounds were more responsible for membrane fouling than hydrophobic components. These results implied that aromatic and hydrophilic substances, in particular protein and polysaccharides were key components of the fouling layers, which need to be considered to enable a reduction of membrane fouling. We thus employed several novel fouling control methods, in which the combination of mono-chloramine pre-treatment and membrane cleaning by NaOH resulted in the recovery up to 86 % of the water from raw AS.

Optimization of alginate bead size immobilized with Chlorella vulgaris and Chlamydomonas reinhardtii for nutrient removal.

Photo-bioreactor experiments using three different size beads (2.0, 3.5, and 5.0 mm) immobilized with two different types of microalgae namely Chlorella vulgaris and Chlamydomonas reinhardtii were conducted to evaluate the nutrient removal efficiency. The highest nutrient removal was obtained at gel bead pore size of 3.5 mm for both species of C. vulgaris and Ch. reinhardtii. 95% removal of T-N and complete reduction of T-P were achieved within 3 stages of treatment in photo-bioreactors containing 20% algal bead volume fraction. Moreover, the results observed by confocal laser scanning microscopy (CLSM) using SYTOX red dye and SYTOX green dye in alginate beads indicated that the effective depth of C. vulgaris and Ch. reinhardtii was about 3.6 mm and 3.0 mm, respectively. This optimized cell immobilization technology would accelerate the nutrient uptake rate of microalgae for improving efficiency of wastewater treatment systems.

Application of volume retarded osmosis - Low pressure membrane hybrid process for recovery of heavy metals in acid mine drainage.

Recovery of heavy metals in acid mine drainage (AMD) such as Mn, Fe, Cu, Zn, As, Cd and Pb was evaluated using volume retarded osmosis and low-pressure membrane (VRO-LPM) process. In VRO-LPM process, the draw solution (DS) is regenerated by the naturally generated pressure, giving its economic value. Ethylenediaminetetraacetic acid tetrasodium salt (EDTA-4Na) and Poly (sodium-4-styrenesulfonate, PSS-Na) were used and compared to determine more suitable DS in heavy metal recovery from the AMD. Forward osmosis (FO) and nanofiltration (NF) membrane were employed in VRO-LPM process, due to the low EDTA-4Na rejection (about 50%) in ultrafiltration (UF) process. For the FO part in the VRO-LPM process, PSS-Na had flux values of 0.12, 0.11 and 0.05 L m-2 h-1 and at osmotic pressure of 8.9, 12 and 13 bar, respectively. Unlike the flux values, the RSF of PSS remained at 0.01 mmol h-1 at all osmotic pressures. For EDTA-4Na, the flux values were 0.10, 0.06 and 0.04 L m-2 h-1, which are relatively higher than those of PSS-Na; and the RSF values were 0.1, 1.2, 2.2 mmol h-1, which are higher compared to those of PSS-Na. Unlike PSS-Na, RSF for EDTA-4Na increased as the concentration increases. In the NF part of the VRO-LPM process, PSS-Na had higher water flux and rejection than EDTA-4Na, and the flux and rejection both decreased with concentration for both PSS-Na and EDTA-4Na. The overall rejection in VRO-LPM process was over 95% for all heavy metal ions. Therefore, VRO-LPM process has proven its ability to be used in AMD treatment for heavy metal removal.

Application of a volume retarded osmosis-low pressure membrane hybrid process for treatment of acid whey.

This study evaluated the treatment of acid whey through a volume-retarded osmosis-low-pressure membrane (VRO-LPM) hybrid process. The VRO-LPM process uses pressure naturally generated inside the closed draw solution (DS) tank to regenerate the DS, making it an economic process. Poly (sodium-4-styrenesulfonate) (PSS) and carboxymethyl cellulose (CMC) were compared to determine which was a more suitable DS for acid whey treatment. Forward osmosis (FO) and ultrafiltration (UF) membranes were used in the VRO-LPM hybrid process because a single UF process showed high water flux and rejection efficiencies above 85% for both PSS and CMC. In both the FO and UF parts of the VRO-LPM process, PSS had a higher water flux than CMC. However, the increasing rate of the feed solution (FS) for CMC was greater than that of PSS, however the overall rejection efficiencies were similar for both DS. Therefore, the VRO-LPM process can be applied to acid whey treatment, and CMC seems to be a better choice of DS than PSS because of its higher concentrating ratio of FS and high overall rejection.

Application of volume-retarded osmosis and low-pressure membrane hybrid process for water reclamation.

A new concept of volume-retarded osmosis and low-pressure membrane (VRO-LPM) hybrid process was developed and evaluated for the first time in this study. Commercially available forward osmosis (FO) and ultrafiltration (UF) membranes were employed in a VRO-LPM hybrid process to overcome energy limitations of draw solution (DS) regeneration and production of permeate in the FO process. To evaluate its feasibility as a water reclamation process, and to optimize the operational conditions, cross-flow FO and dead-end mode UF processes were individually evaluated. For the FO process, a DS concentration of 0.15 g mL-1 of polysulfonate styrene (PSS) was determined to be optimal, having a high flux with a low reverse salt flux. The UF membrane with a molecular weight cut-off of 1 kDa was chosen for its high PSS rejection in the LPM process. As a single process, UF (LPM) exhibited a higher flux than FO, but this could be controlled by adjusting the effective membrane area of the FO and UF membranes in the VRO-LPM system. The VRO-LPM hybrid process only required a circulation pump for the FO process. This led to a decrease in the specific energy consumption of the VRO-LPM process for potable water production, that was similar to the single FO process. Therefore, the newly developed VRO-LPM hybrid process, with an appropriate DS selection, can be used as an energy efficient water production method, and can outperform conventional water reclamation processes.

New concept of pump-less forward osmosis (FO) and low-pressure membrane (LPM) process.

We tested the possibility of energy-saving water treatment methods by using a pump-less forward osmosis (FO) and low-pressure membrane (LPM) hybrid process (FO-LPM). In this pump-less FO-LPM, permeate migrates from the feed solution (FS) to the draw solution (DS) through the FO membrane by use of osmotic pressure differences. At the same time, within the closed DS tank, inner pressure increases as the DS volume increases. By using the DS tank's internal pressure, the LPM process works to re-concentrate the diluted DS, maintaining the DS concentration and producing clean water. In this study, a polymer - polystyrene sulfonate (PSS) was used as a draw solute. Based on the results of each individual portion of the process, the optimal range of the PSS DS was determined. The performance of the pump-less FO-LPM process was lower than that of a single process; however, we observed that the hybrid process can be operated without a pump for regeneration of a diluted DS. This research highlights the feasibility and applicability of pump-less FO-LPM processes using a polymeric DS for water treatment. Additionally, it is suggested that this novel process offers a breakthrough in FO technology that is often limited by operation and management cost.