Climate change and future water demand: Implications for chlorine and trihalomethanes management in water distribution systems.

The global change in surface water quality calls for increased preparedness of drinking water utilities. The increasing frequency of extreme climatic events combined with global warming can impact source and treated water characteristics such as temperature and natural organic matter. On the other hand, water saving policies in response to water and energy crisis in some countries can aggravate the situation by increasing the water residence time in the drinking water distribution system (DWDS). This study investigates the individual and combined effect of increased dissolved organic carbon (DOC), increased temperature, and reduced water demand on fate and transport of chlorine and trihalomethanes (THMs) within a full-scale DWDS in Canada. Chlorine and THM prediction models were calibrated with laboratory experiments and implemented in EPANET-MATLAB toolkit for prediction in the DWDS under different combinations of DOC, temperature, and demand. The duration of low chlorine residuals (<0.2 mg/L) and high THM (>80 µg/L) periods within a day in each scenario was reported using a reliability index. Low-reliability zones prone to microbial regrowth or high THM exposure were then delineated geographically on the city DWDS. Results revealed that water demand reduction primarily affects chlorine availability, with less concern for THM formation. The reduction in nodal chlorine reliability was gradual with rising temperature and DOC of the treated water and reducing water demand. Nodal THM reliability remained unchanged until certain thresholds were reached, i.e., temperature >25 °C for waters with DOC <1.52 mg/L, and DOC >2.2 mg/L for waters with temperature = 17 °C. At these critical thresholds, an abrupt network-wide THM exceedance of 80 µg/L occurred. Under higher DOC and temperature levels in future, employing the proposed approach revealed that increasing the applied chlorine dosage (which is a conventional method used to ensure sufficient chlorine coverage) results in elevated exposure toTHMs and is not recommended. This approach aids water utilities in assessing the effectiveness of different intervention measures to solve water quality problems, identify site-specific thresholds leading to major decreases in system reliability, and integrate climate adaptation into water safety management.

Impact of Cleaning on Membrane Performance during Surface Water Treatment: A Hybrid Process with Biological Ion Exchange and Gravity-Driven Membranes.

In this study, the hybrid biological ion exchange (BIEX) resin and gravity-driven membrane (GDM) process was employed for the treatment of coloured and turbid river water. The primary objective was to investigate the impact of both physical and chemical cleaning methods on ceramic and polymeric membranes in terms of their stabilised flux, flux recovery after physical/chemical cleaning, and permeate quality. To address these objectives, two types of MF and UF membranes were utilised (M1 = polymeric MF, M2 = polymeric UF, M3 = ceramic UF, and M4 = lab-made ceramic MF). Throughout the extended operation, the resin functioned initially in the primary ion exchange (IEX) region (NOM displacement with pre-charged chloride) and progressed to a secondary IEX stage (NOM displacement with bicarbonate and sulphate), while membrane flux remained stable. Subsequently, physical cleaning involved air/water backwash with two different flows and pressures, and chemical cleaning utilised NaOH at concentrations of 20 and 40 mM, as well as NaOCl at concentrations of 250 and 500 mg Cl2/L. These processes were carried out to assess flux recovery and identify fouling reversibility. The results indicate an endpoint of 1728 bed volumes (BVs) for the primary IEX region, while the secondary IEX continued up to 6528 BV. At the end of the operation, DOC and UVA254 removal in the effluent of the BIEX columns were 68% and 81%, respectively, compared to influent water. This was followed by 30% and 57% DOC and UVA254 removal using M4 (ceramic MF). The stabilised flux remained approximately 3.8-5.2 LMH both before and after the cleaning process, suggesting that membrane materials do not play a pivotal role. The mean stabilised flux of polymeric membranes increased after cleaning, whereas that of the ceramics decreased. Enhanced air-water backwash flow and pressure resulted in an increased removal of hydraulic reversible fouling, which was identified as the dominant fouling type. Ceramic membranes exhibited a higher removal of reversible hydraulic fouling than polymeric membranes. Chemical cleaning had a low impact on flux recovery; therefore, we recommend solely employing physical cleaning.

Galectin-1 Modulates the Fusogenic Activity of Placental Endogenous Retroviral Envelopes.

Syncytin-1 and -2 are glycoproteins encoded by human endogenous retrovirus (hERV) that, through their fusogenic properties, are needed for the formation of the placental syncytiotrophoblast. Previous studies suggested that these proteins, in addition to the EnvP(b) envelope protein, are also involved in other cell fusion events. Since galectin-1 is a ß-galactoside-binding protein associated with cytotrophoblast fusion during placental development, we previously tested its effect on Syncytin-mediated cell fusion and showed that this protein differently modulates the fusogenic potential of Syncytin-1 and -2. Herein, we were interested in comparing the impact of galectin-1 on hERV envelope proteins in different cellular contexts. Using a syncytium assay, we first demonstrated that galectin-1 increased the fusion of Syncytin-2- and EnvP(b)-expressing cells. We then tested the infectivity of Syncytin-1 and -2 vs. VSV-G-pseudotyped viruses toward Cos-7 and various human cell lines. In the presence of galectin-1, infection of Syncytin-2-pseudotyped viruses augmented for all cell lines. In contrast, the impact of galectin-1 on the infectivity of Syncytin-1-pseudotyped viruses varied, being cell- and dose-dependent. In this study, we report the functional associations between three hERV envelope proteins and galectin-1, which should provide information on the fusogenic activity of these proteins in the placenta and other biological and pathological processes.

Modeling the fate of viruses in aquifers: Multi-kinetics reactive transport, risk assessment, and governing parameters.

The transport of viruses in groundwater is a complex process controlled by both hydrodynamic and reaction parameters. Characterizing the transport of viruses in groundwater is of crucial importance for investigating health risks associated with groundwater consumption from private individual or residential pumping wells. Setback distances between septic systems, which are the source of viruses, and pumping wells must be designed to offer sufficient groundwater travel times to allow the viral load to degrade sufficiently to be acceptable for community health needs. This study consists of developing numerical simulations for the reactive transport of viruses in the subsurface. These simulations are validated using published results of laboratory and field experiments on virus transport in the subsurface and applying previously developed analytical solutions. The numerical model is then exploited to investigate the sensitivity of the fate of viruses in saturated porous media to hydraulic parameters and the coefficients of kinetic reactions. This sensitivity analysis provides valuable insights into the prevailing factors governing health risks caused by contaminated water in private wells in rural residential contexts. The simulations of virus transport are converted into health risk predictions through dose-response relationships. Risk predictions for a wide range of input parameters are compared with the international regulatory health risk target of a maximum of 10-4 infections/person/year and a 30 m setback distance to identify critical subsurface contexts that should be the focus of regulators.

Anionic and Ampholytic High-Amylose Starch Derivatives as Excipients for Pharmaceutical and Biopharmaceutical Applications: Structure-Properties Correlations.

Many chemical modifications of starch are realized in organic (mostly methanol) phase, allowing high degrees of substitution (DS). Some of these materials are used as disintegrants. To expand the usage of starch derivative biopolymers as drug delivery system, various starch derivatives obtained in aqueous phase were evaluated with the aim to identify materials and procedures which would generate multifunctional excipients providing gastro-protection for controlled drug delivery. Chemical, structural and thermal characteristics of anionic and ampholytic High Amylose Starch (HAS) derivatives under powder (P), tablet (T) and film (F) forms were evaluated by X-ray Diffraction (XRD), Fourier Transformed Infrared (FTIR) and thermogravimetric analysis (TGA) methods and correlated with the behavior of tablets and films in simulated gastric and intestinal media. At low DS, the HAS carboxymethylation (CMHAS) in aqueous phase, generated tablets and films that were insoluble at ambient conditions. The CMHAS filmogenic solutions, with a lower viscosity, were easier to cast and gave smooth films without the use of plasticizer. Correlations were found between structural parameters and the properties of starch excipients. Compared to other starch modification procedures, the aqueous modification of HAS generated tunable multifunctional excipients that may be recommended for tablets and functional coatings for colon-targeted formulations.

Article Application of neural network in metal adsorption using biomaterials (BMs): a review.

With growing environmental consciousness, biomaterials (BMs) have garnered attention as sustainable materials for the adsorption of hazardous water contaminants. These BMs are engineered using surface treatments or physical alterations to enhance their adsorptive properties. The lab-scale methods generally employ a One Variable at a Time (OVAT) approach to analyze the impact of biomaterial modifications, their characteristics and other process variables such as pH, temperature, dosage, etc., on the removal of metals via adsorption. Although implementing the adsorption procedure using BMs seems simple, the conjugate effects of adsorbent properties and process attributes implicate complex nonlinear interactions. As a result, artificial neural networks (ANN) have gained traction in the quest to understand the complex metal adsorption processes on biomaterials, with applications in environmental remediation and water reuse. This review discusses recent progress using ANN frameworks for metal adsorption using modified biomaterials. Subsequently, the paper comprehensively evaluates the development of a hybrid-ANN system to estimate isothermal, kinetic and thermodynamic parameters in multicomponent adsorption systems.

Infection of the Ex Vivo Tonsil Model by HTLV-1 Envelope-Pseudotyped Viruses.

Human T-cell leukemia virus type 1 (HTLV-1) is the causal agent of adult T-cell leukemia/lymphoma and HTLV-1-associated myelopathy/tropical spastic paraparesis. Its tropism is known to be broad in cultured cell lines, while in vivo data support a more selective transmission toward CD4+ T cells and the limited targeting of other hematopoietic cell types. An essential condition for HTLV-1 infection is cell-to-cell contact, to which both virological synapse and viral biofilm have been suggested to strongly contribute. As cell lines and animal models each present their own limitations in studying HTLV-1 replication, we have explored the use of an ex vivo model based on the secondary lymphoid tonsillar tissue. HIV-1 luciferase-expressing pseudotyped viruses bearing the HTLV-1 envelope protein at their surface were first shown to recapitulate the wide spectrum of infectivity of HTLV-1 toward various cell lines. Tonsil fragments were next exposed to pseudotyped viruses and shown to be reproducibly infected. Infection by HTLV-1 Env-pseudotyped viruses was blocked by different anti-gp46 antibodies, unlike infection by HIV-1 virions. The dose-dependent infection revealed a gradual increase in luciferase activity, which was again sensitive to anti-gp46 antibodies. Overall, these results suggest that the ex vivo tonsil model represents a reliable alternative for studying HTLV-1 replication and potentially viral latency, as well as early clonal formation.

Cadmium affects autophagy in the human intestinal cells Caco-2 through ROS-mediated ERK activation.

Cadmium is a toxic metal that enters the food chain. Following oral ingestion, the intestinal epithelium has the capacity to accumulate high levels of this metal. We have previously shown that Cd induces ERK1/2 activation in differentiated but not proliferative human enterocytic-like Caco-2 cells. As autophagy is a dynamic process that plays a critical role in intestinal mucosa, we aimed the present study 1) to investigate the role of p-ERK1/2 in constitutive autophagy in proliferative Caco-2 cells and 2) to investigate whether Cd-induced activation of ERK1/2 modifies autophagic activity in postconfluent Caco-2 cell monolayers. Western blot analyses of ERK1/2 and autophagic markers (LC3, SQSTM1), and cellular staining with acridine orange showed that ERK1/2 and autophagic activities both decreased with time in culture. GFP-LC3 fluorescence was also associated with proliferative cells and the presence of a constitutive ERK1/2-dependent autophagic flux was demonstrated in proliferative but not in postconfluent cells. In the latter condition, serum and glucose deprivation triggered autophagy via a transient phosphorylation of ERK1/2, whereas Cd-modified autophagy via a ROS-dependent sustained activation of ERK1/2. Basal autophagy flux in proliferative cells and Cd-induced increases in autophagic markers in postconfluent cells both involved p-ERK1/2. Whether Cd blocks autophagic flux in older cell cultures remains to be clarified but our data suggest dual effects. Our results prompt further studies investigating the consequences that Cd-induced ERK1/2 activation and the related effect on autophagy may have on the intestinal cells, which may accumulate and trap high levels of Cd under some nutritional conditions.

A newly identified interaction between nucleolar NPM1/B23 and the HTLV-I basic leucine zipper factor in HTLV-1 infected cells.

Human T-cell leukemia virus type 1 is the causative agent of HTLV-1-associated myelopathy/tropical spastic paraparesis and adult T-cell leukemia-lymphoma (ATL). The HTLV-1 basic leucine zipper factor (HBZ) has been associated to the cancer-inducing properties of this virus, although the exact mechanism is unknown. In this study, we identified nucleophosmin (NPM1/B23) as a new interaction partner of HBZ. We show that sHBZ and the less abundant uHBZ isoform interact with nucleolar NPM1/B23 in infected cells and HTLV-1 positive patient cells, unlike equivalent antisense proteins of related non-leukemogenic HTLV-2, -3 and-4 viruses. We further demonstrate that sHBZ association to NPM1/B23 is sensitive to RNase. Interestingly, sHBZ was shown to interact with its own RNA. Through siRNA and overexpression experiments, we further provide evidence that NPM1/B23 acts negatively on viral gene expression with potential impact on cell transformation. Our results hence provide a new insight over HBZ-binding partners in relation to cellular localization and potential function on cell proliferation and should lead to a better understanding of the link between HBZ and ATL development.

Rapid Assessment of Biological Activity of Ag-Based Antiviral Coatings for the Treatment of Textile Fabrics Used in Protective Equipment Against Coronavirus.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its variants have rapidly spread worldwide, causing coronavirus disease (COVID-19) with numerous infected cases and millions of deaths. Therefore, developing approaches to fight against COVID-19 is currently the most priority goal of the scientific community. As a sustainable solution to stop the spread of the virus, a green dip-coating method is utilized in the current work to prepare antiviral Ag-based coatings to treat cotton and synthetic fabrics, which are the base materials used in personal protective equipment such as gloves and gowns. Characterization results indicate the successful deposition of silver (Ag) and stabilizers on the cotton and polypropylene fiber surface, forming Ag coatings. The deposition of Ag and stabilizers on cotton and etched polypropylene (EPP) fabrics is dissimilar due to fiber surface behavior. The obtained results of biological tests reveal the excellent antibacterial property of treated fabrics with large zones of bacterial inhibition. Importantly, these treated fabrics exhibit an exceptional antiviral activity toward human coronavirus OC43 (hCoV-OC43), whose infection could be eliminated up to 99.8% when it was brought in contact with these fabrics after only a few tens of minutes. Moreover, the biological activity of treated fabrics is well maintained after a long period of up to 40 days of post-treatment.

Removal of Zwitterionic PFAS by MXenes: Comparisons with Anionic, Nonionic, and PFAS-Specific Resins.

Zwitterionic per- and polyfluoroalkyl substances are increasingly detected in aquatic environments. The magnitude of their concentration and increased frequency of detection worldwide raise questions on their presence in drinking water and associated health risk. Scientific knowledge on the identification of treatment technologies to effectively capture such zwitterionic PFAS from contaminated water sources remains largely unknown. In this study, we investigated the application of anionic organic scavenger ion exchange (IX) resins (A860), nonionic IX resins (XAD 4 and XAD 7), PFAS-specific resins (A694 and A592), and Ti3C2 MXenes (novel two-dimensional metal carbides) for the removal of select fluorotelomer zwitterionic PFAS from natural waters. The cumulative removal of zwitterionic PFAS at pH ∼ 7 follows the order: Ti3C2 MXenes > A694 > A592 > A860 > XAD 4 ∼ XAD 7. Ti3C2 MXenes were able to capture >75% of the total influent zwitterionic PFAS and the performance remained consistent in natural and synthetic water. Ti3C2 MXenes also exhibited efficient regeneration (>90% recovery) with 0.4 M Na2SO3 solution, while the regeneration efficacy of other IX resins generally remained below 20%. Treatment with ∼180 J/cm2 UV dosage in the 0.4 M Na2SO3 regenerant brine solution yielded >99.9% reduction in the zwitterionic PFAS concentration indicating that UV-sulfite systems exhibit promising potential for the treatment of zwitterionic PFAS concentrates.

Elucidating the removal of organic micropollutants on biological ion exchange resins.

Biological ion exchange (BIEX) refers to operating ion exchange (IX) filters with infrequent regeneration to favor the microbial growth on resin surface and thereby contribute to the removal of organic matter through biodegradation. However, the extent of biodegradation on BIEX resins is still debatable due to the difficulty in discriminating between biodegradation and IX. The objective of the present study was to evaluate the performance of BIEX resins for the removal of organic micropollutants and thereby validate the occurrence of biodegradation. The removals of biodegradable micropollutants (neutral: caffeine and estradiol; negative: ibuprofen and naproxen) and nonbiodegradable micropollutants with different charges (neutral: atrazine and thiamethoxam; negative: PFOA and PFOS) were respectively monitored during batch tests with biotic and abiotic BIEX resins. Results demonstrated that biodegradation contributed to the removal of caffeine, estradiol, and ibuprofen, confirming that biodegradation occurred on the BIEX resins. Furthermore, biodegradation contributed to a lower extent to the removal of naproxen probably due to the absence of an adapted bacterial community (Biotic: 49% vs Abiotic: 38% after 24 h batch test). The removal of naproxen, PFOS, and PFOA were attributable to ion exchange with previously retained natural organic matter on BIEX resins. Nonbiodegradable and neutral micropollutants (atrazine and thiamethoxam) were minimally (6%-10%) removed during the batch tests. Overall, the present study corroborates that biomass found on BIEX resins contribute to the removal of micropollutants through biodegradation and ion exchange resins can be used as biomass support for biofiltration.

Biological ion exchange as an alternative to biological activated carbon for natural organic matter removal: Impact of temperature and empty bed contact time (EBCT).

Biofiltration is a widely used process in drinking water treatment plants to remove natural organic matter (NOM). A novel biofiltration process using ion exchange resins as supporting media (i.e., biological ion exchange or BIEX) has been demonstrated to provide a superior performance compared to conventional biological activated carbon (BAC). In order to optimize the performance of BIEX filters, the impact of temperature and empty bed contact time (EBCT) on NOM removal was systematically studied. In the present study, bench-scale BIEX filters were set up in parallel with BAC filters and operated at different temperatures (i.e., 4 °C, 10 °C and 20 °C) and EBCTs (i.e., 7.5 min, 15 min and 30 min). Higher average dissolved organic carbon (DOC) removal was achieved in BIEX filters (73 ± 6%) than BAC filters (22 ± 9%) at the steady state with an EBCT of 30 min. Higher temperatures improved NOM removal in both BAC and BIEX filters, with the impact being greater at lower EBCTs (i.e., 7.5 min and 15 min). Higher EBCTs could also improve NOM removal, with the impact being greater at lower temperatures (i.e., 4 °C and 10 °C). DOC removal for BIEX and BAC filters can be modeled with a first-order kinetic model (R2 = 0.93-0.99). BAC had a higher temperature activity coefficient than BIEX (1.0675 vs. 1.0429), indicating that temperature has a greater impact on BAC filtration than BIEX filtration. Overall, temperature and EBCT must be considered simultaneously for biofilters to efficiently remove NOM.

Application of MXenes for water treatment and energy-efficient desalination: A review.

MXenes are a new type of two-dimensional (2D) material which are rapidly gaining traction for a range of environmental, chemical and medical applications. MXenes and MXene-composites exhibit high surface area, superlative chemical stability, thermal conductivity, hydrophilicity and are environmentally compatible. Consequently, MXenes have been successfully employed for hydrogen storage, semiconductor manufacture and lithium ion batteries. In recent years, MXenes have been utilized in numerous environmental applications for treating contaminated surface waters, ground and industrial/ municipal wastewaters and for desalination, often outperforming conventional materials in each field. MXene-composites can adsorb multiple organic and inorganic contaminants, and undergo Faradaic capacitive deionization (CDI) when utilized for electrochemical applications. This approach allows for a significant decrease in the energy demand by overcoming the concentration polarization limitation of conventional CDI electrodes, offering a solution for low-energy desalination of brackish waters. This article presents a state-of-the-art review on water treatment and desalination applications of MXenes and MXene-composites. An investigation into the kinetics and isotherms is presented, as well as the impact of water constituents and operating conditions are also discussed. The applications of MXenes for CDI, pervaporation desalination and solar thermal desalination are also examined based on the reviewed literature. The effects of the water composition and operational protocols on the regeneration efficacy and long-term usage are also highlighted.

Alleviating the burden of ion exchange brine in water treatment: From operational strategies to brine management.

Ion exchange (IX) using synthetic resins is a cost-efficient technology to cope with a wide range of contaminants in water treatment. However, implementing IX processes is constrained by the regeneration of IX resins that generates a highly concentrated brine (i.e., IX brine), the disposal of which is costly and detrimental to ecosystems. In an effort to make the application of IX resins more sustainable in water treatment, substantial research has been conducted on the optimization of IX resins operation and the management of IX brine. The present review critically evaluates the literature surrounding IX operational strategies and IX brine management which can be used to limit the negative impacts arising from IX brine. To this end, we first analyzed the physicochemical characteristics of brines from the regeneration of IX resins. Then, we critically evaluated IX operational strategies that facilitate brine management, including resin selection, contactor selection, operational modes, and regeneration strategies. Furthermore, we analyzed IX brine management strategies, including brine reuse and brine disposal (without or with treatment). Finally, a novel workflow for the IX water treatment plant design that integrates IX operational strategies and IX brine management is proposed, thereby highlighting the areas that make IX technology more sustainable for water treatment.

Kinetics and Monte Carlo simulation of UV disinfection of B. subtilis spores and SARS-CoV-2 in dried saliva droplets.

Surfaces can be contaminated by droplets produced through coughing or sneezing. In this exploratory work, the UV disinfection results of Bacillus subtilis spores in dried saliva droplets were fitted to a three-parameter kinetic model (R2 ≥ 0.97). This model has a disinfection rate constant for single organisms and a smaller one for aggregates found in droplets. The fraction of organisms found in aggregates (ß) could account for the effects of different-sized droplets in the experimental work. Since a wide spectrum of droplet sizes can be produced, and some of the rate constants were uncertain, Monte Carlo simulation was used to estimate the UV inactivation performance in dried saliva droplets in a variety of conditions. Using conservative distribution for ß, the model was applied to the UV disinfection of SARS-CoV-2 in dried saliva droplets. It was shown that a one-log reduction of SARS-CoV-2 was very likely (p>99.9%) and a two-log reduction was probable (p=75%) at a dose of 60 mJ/cm2. Aggregates tend to be variable and limit the log reductions that can be achieved at high UV doses.

Performance of conventional drinking water treatment following dispersant remediation of an oil spill in surface water.

Physical remediation such as the use of booms has been applied for most oil-spill cleanup activities in surface water. The application of dispersants has been controversial primarily due to the unknown impacts on drinking water sources. This study investigated changes in surface water quality following dispersant application to crude oil spills and the subsequent impact on the efficiency of ballasted flocculation, a physicochemical treatment process applied in many drinking water treatment plants (DWTP). Contamination of surface water was performed in the presence of crude oil concentrations (109 ± 13 mg/L) with and without dispersants. Water quality parameters such as turbidity and UVA254 were monitored and ballasted flocculation efficiency was assessed based on water quality as well as the removal of oil droplets, residual dispersant, and petroleum hydrocarbons as total organic carbon (TOC). Results showed that the measured water quality parameters except TOC are unsuitable indicators of petroleum hydrocarbon contamination in surface water. However, TOC lacked sensitivity when used in settled water to detect hydrocarbon contaminants. Although ballasted flocculation efficiency was not limited by the presence of crude oil and low dispersant concentrations when an optimized alum dose was applied (41 mg dry alum/L), the process was unable to remove other dispersant-related compounds that are not identifiable by the monitored water quality parameters. Measured concentrations of these compounds in settled waters were above the U.S. EPA's aquatic life benchmark (40 µg/L). Findings would be beneficial to DWTP in their efforts to upgrade their treatment processes and prepare oil-spill contingency plans.

A photo-Fenton nanocomposite ultrafiltration membrane for enhanced dye removal with self-cleaning properties.

Membrane fouling is an ongoing challenge in the membrane filtration process. Herein, a photocatalytic membrane comprising a reactive layer was fabricated by engineering partially reduced graphene oxide/Ag nanoparticles/MIL-88A (prGO/Ag/M88A, pGAM) photocatalysts on the PVDF substrate membranes. Benefiting from the high conductivity of prGO and the surface plasmon resonance (SPR) effect of Ag nanoparticles (Ag NPs), the photo-sensitivity of the prGO/Ag/M88A is significantly enhanced. Compared to the membrane in the dark condition, the pGAM membrane displayed an enhanced dye removal efficiency (∼99.7%) and significantly improved permeability (∼189 L·m-2·h-1 bar-1) towards dye contaminants based on the synergistic filtration/photo-Fenton processes. Significantly, the membrane retained high perm-selectivity after 10 cyclic runs (183 L·m-2·h-1 bar-1 of permeability and 98.1% of dye removal), and its nano-channel structure did not collapse under high pressure (0.1-0.4 MPa). The membrane also exhibits antifouling properties with a high water flux recovery of more than 90%. In addition, the pGAM membrane exhibited a high MB degradation efficiency (∼90%) when it is directly used as a photocatalyst in the photo-Fenton system. The mechanism of the self-cleaning is also proposed through quenching experiments. The results of this study demonstrate that this self-cleaning membrane has huge promise for membrane anti-fouling and wastewater remediation.

Modeling the efficiency of UV at 254 nm for disinfecting the different layers within N95 respirators.

The study presented a Monte Carlo simulation of light transport in eight commonly used filtered facepiece respirators (FFRs) to assess the efficacy of UV at 254 nm for the inactivation of SARS-CoV-2. The results showed different fluence rates across the thickness of the eight different FFRs, implying that some FFR models may be more treatable than others, with the following order being (from most to least treatable): models 1512, 9105s, 1805, 9210, 1870+, 8210, 8110s and 1860, for single side illumination. The model predictions did not coincide well with some previously reported experimental data on virus inactivation when applied to FFR surfaces. The simulations predicted that FFRs should experience higher log reductions (>>6-log) than those observed experimentally (often limited to ~5-log). Possible explanations are virus shielding by aggregation or soiling, and a lack of the Monte Carlo simulations considering near-field scattering effects that can create small, localized regions of low UV photon probability on the surface of the fiber material. If the latter is the main cause in limiting practical UV viral decontamination, improvement might be achieved by exposing the FFR to UV isotropically from all directions, such as by varying the UV source to the FFR surface angle during treatment.

Towards Water, Sodium Chloride and Natural Organic Matter Recovery from Ion Exchange Spent Brine.

Despite the tremendous success of the application of anion exchange resins (IX) in natural organic matter (NOM) removal over conventional removal methods, the considerable amount of brine spent during its regeneration cycle makes its sustainability questionable. This polluting saline stream can be challenging to manage and costly to discharge. Alternatively, and with the recent shift in perception of resource recovery, the produced spent brine can no longer be seen as a polluting waste but as an unconventional source of water, minerals and nutrients. In this research, for the first time, we evaluated the effectiveness of an integrated monovalent selective electrodialysis (MSED) and direct contact membrane distillation (DCMD) system in IX spent brine desalination and resource recovery. Of particular interest were the effects of operating time on the characteristics of the monovalent permselective ion exchange membranes, the impact of the DCMD stack configuration on minimizing heat loss to the ambient environment and the efficacy of the recovered NaCl in the regenerating cycle of the exhausted IXs. Our findings demonstrated that although the recovered NaCl from the stand-alone MSED can restore nearly 60% ion exchange capacity of the exhausted IXs, coupling MSED with DCMD led to minimizing the consumption of fresh NaCl (in the IX regeneration cycle) significantly, the potential application of NOM in agriculture and diminishing the risk of the IX spent brine disposal. In addition, the initial characteristics of the ion permselective membranes were maintained after 24 h of MSED and the transmembrane flux was increased when the feed/hot compartment (in the DCMD stack) was encapsulated on two outer ends with coolant/permeate compartments as a result of less heat loss to the ambient environment.