Chlorine Resistance Research Articles

Creating smart chlorine-resistant polyamide reverse osmosis membranes via self-healing temperature-responsive nanocontainer functionalization

We present an innovative solution for improving the chlorine resistance of polyamide RO membranes. Our method involves the design of temperature-specific (70 ℃) responsive nanocontainers (T-RNC) through layer-by-layer self-assembly on a monodisperse SiO2 nanoparticle core. These nanocontainers, measuring 25 nm in size, are embedded within a thin film nanocomposite (TFN) membrane, resulting in a homogeneous surface structure with increased roughness and strong hydrophilicity. The precise temperature-responsive properties of T-RNC enable the dissolution of the encapsulated shell material, releasing SS molecules containing amino and carboxyl groups. These molecules effectively bind to broken amid bonds within the PA layer, repairing structural damage caused by chlorination and significantly enhancing the membrane’s chlorine resistance. Extensive testing revealed that the temperature-responsive TFN membrane maintained over 90 % NaCl rejection, even after exposure to 18,000 ppm.h of chlorination. In contrast, the control group lacking temperature-responsive TFN and TFC membranes exhibited reduced rejection rates of 62.15 % and 71.24 %, respectively. Additionally, the TFN membranes exhibited excellent water permeability and resistance to contamination. Our findings offer promising avenues for researchers to explore the development of intelligent and chlorine-resistant polyamide RO membranes, with a particular focus on chlorination-remediation techniques.

Modeling the health impact of wastewater contamination events in drinking water networks

Pathogen intrusion in drinking water systems can pose severe health risks. To better prepare in planning and responding to such events, computational models that capture the intrusion and health impact dynamics are needed. This study presents a novel benchmark testbed that integrates current knowledge on pathogen transport and fate in chlorinated systems and can assess infection risk from contamination events. The model considers organic matter degradation, chlorine decay mechanisms, pathogen inactivation kinetics, as well as stochastic water demands.We studied modeling of wastewater intrusion events that can occur anywhere within a chlorinated and non-chlorinated network. We applied the Quantitative Microbial Risk Assessment framework focusing on three pathogens: enterovirus, Campylobacter, and Cryptosporidium, and their respective dose-response models. Synthetic household-level water demand time series were used to model the individual water consumption timing and calculate the infection risk (exposure via ingestion).Model outcomes indicate that while chlorination aids mitigation, larger contaminations can still lead to infections due to chlorine resistance (for Cryptosporidium) and chlorine depletion at the contamination point. In our example scenarios, chlorine-susceptible pathogens infected of the downstream population, while chlorine-resistant ones infected the entire downstream population. Enterovirus infection risk is higher, despite the concentrations in the contamination source being lower, due to the lower susceptibility to chlorine than Campylobacter. In non-chlorinated networks, the modeled wastewater contamination events led to infection risk in the total population, depending on the contamination location. Hydraulic uncertainty had a limited influence on infection risk. Furthermore, Campylobacter’s infection risk is more sensitive to the initial concentration in the contamination source whereas enterovirus infection risk to the inactivation rate. The model further indicates that the time window for effective mitigation of the magnitude of a waterborne outbreak is short (within hours).

Effect of Pipe Materials and Interspecific Interactions on Biofilm Formation and Chlorine Resistance: Turn Enemies into Friends

Drinking water distribution systems (DWDSs) may be contaminated to various degrees when different microorganisms attach to the pipe walls. Understanding the characteristics of biofilms on pipe walls can help prevent and control microbial contamination in DWDSs. The biofilm formation, interspecific interactions, and chlorine resistance of 10 dual-species biofilms in polyethylene (PE) and cast iron (CI) pipes were investigated in this paper. The biofilm biomass (heterotrophic bacterial plate count and crystal violet) of dual species in CI pipes is significantly higher than that in PE pipes, but the biofilm activity in CI pipes is significantly lower than that in PE pipes. The interspecific interaction of Sphingomonas-containing group presented synergistic or neutral relationship in PE pipes, whereas the interspecific interaction of the Acidovorax-containing group showed a competitive relationship in CI pipes. Although interspecific relationships may help bacteria resist chlorine, the chlorine resistance was more reliant on dual-species groups and pipe materials. In CI pipes, the Microbacterium containing biofilm groups showed better chlorine resistance, whereas in PE pipes, most biofilm groups with Bacillus exhibited better chlorine resistance. The biofilm groups with more extracellular polymeric substance (EPS) secretion showed stronger chlorine resistance. The biofilm in the PE pipe is mainly protected by EPS, while both EPS and corrosion products shield the biofilms within CI pipe. These results supported that dual-species biofilms are affected by pipe materials and interspecific interactions and provided some ideas for microbial control in two typical pipe materials.

Coordination dependent photocatalytic peroxymonosulfate activation on biomass derived Fe single atom catalysts for atrazine degradation

Challenges associated with uncontrollable metal coordination structures in biomass-derived single-atom catalysts (SACs) and their intricate impacts on photocatalytic peroxymonosulfate (PMS) activation pose significant hurdles for the application of photo-Fenton technology towards wastewater treatment. Herein, we employed a co-pyrolysis strategy using Enteromorpha prolifera (E. prolifera) to synthesize Fe SACs with varying Fe–NX coordination, i.e., Fe–N5 and Fe–N6. Fe–N6-based SAC achieved over 80% atrazine (ATZ) degradation in 15 min, with a degradation rate of 0.13 min−1, representing 2.6-fold improvement over SAC with Fe–N5 structure. Experimental and simulation results revealed that Fe–N6 active sites acted as electron donors, enhancing the delocalization of π-electrons and improving photocatalytic PMS activation. This SAC also exhibited high selectivity for 1O2 degradation pathway and impressive ATZ degradation in seawater, with notable chlorine resistance, underscoring its potential in environmental pollutant remediation. This work unveils the catalyst structure-photocatalytic PMS activation performance relationship, offering avenue for developing more sustainable and efficient biomass-derived SACs for wastewater treatment.

Incorporation of Graphene Oxide Quantum Dots in Gradient Layers of Polyethersulphone Nanofiltration Membranes for Nitrate Rejection from Aqueous Solution.

Graphene oxide quantum dots (GOQDs) have been widely used to prepare nanofiltration membranes due to the merits of excellent dispersity, ultrasmall size, and unique properties related to graphene. In this study, we first prepared the polyethersulphone-based nanofiltration (PES-NF) membrane via an interfacial polymerization process using a piperazine and m-phenylenediamine mixed solution as the aqueous phase. Then GOQDs were incorporated into the top-down gradient structured layers (i.e., ultrathin layer, interlayer, and substrate membrane layer) of the nanofiltration membrane, and subsequently the effect of GOQD addition on the nitrate rejection was evaluated. Compared with the pristine PES-NF membrane without the incorporation of GOQDs, the fabricated NF membrane (GOQD/PES-NF-2) incorporating GOQDs at both the ultrathin layer and interlayer exhibits more remarkable performances (an acceptable permeation flux of 52.2 L m-1 h-1 and excellent nitrate rejection of 96.3% at 0.6 MPa), the permeation flux of this membrane increases by nearly 2.4 times, and its nitrate rejection also shows a slight enhancement (∼7.6%) compared with those of PES-NF. Remarkably, at the operating pressure much lower than that required by reverse osmosis membranes, the GOQD/PES-NF-2 membrane possesses an equivalent monovalent ion rejection to reverse osmosis membranes but a higher permeation flux. Furthermore, the result of a 7 day continuous stability test validates the excellent durability of the GOQD/PES-NF-2 membrane, and its antifouling and chlorine resistance performances also outperform those of the PES-NF membrane.

Fabrication of green xylose-based nanofiltration membrane with enhanced performance and chlorine resistance

Nanofiltration technology has been widely used in drinking water purification due to its excellent permeance and selectivity properties, especially in small molecular solute separation. However, using oxidizing agents in the pretreatment process for fouling control threatens the nanofiltration membrane structure, leading to the deterioration of the separation performance. Herein, we fabricate a polyester nanofiltration membrane utilizing xylose as an aqueous monomer in the interfacial polymerization process. Due to abundant hydroxyl groups and low reactivity of xylose monomers, the polyester membrane possessed a hydrophilic and thin separation layer, which led to high water permeance with the optimal value of 28.7 L·m−2·h−1·bar−1. Possessing highly cross-linking structures and negatively charged surfaces, the fabricated polyester membranes showed an excellent Na2SO4 rejection of up to 95.4 %. In addition, the low electron-donating property of polyester membranes ensured their chemical stability toward active chlorine. This endows relatively stable performance of the polyester membrane after chlorine resistance tests in a wide pH range. This study presents a feasible approach employing green monomers for fabricating nanofiltration membranes with outstanding separation performance and robust chlorine resistance.

Fabrication of POSS-centered polyester network as high anti-chlorine and anti-fouling separation layer of membrane via successive Photo-ATRP and interfacial polymerization for molecular separation

The incorporation of polyhedral oligomeric sesquisiloxane (POSS), a distinctive nanoparticle, into the membrane separation layer represents an effective strategy for enhancing the chlorine resistance of membranes. This modification contributes to both the durability of the membrane and its separation efficiency. However, POSS is easy to agglomerate, which affects the separation performance of the membrane. In this paper, POSS-centered polyhydroxy polymer (OMEPOSS-P(GMA-NMDG)) was synthesized via photo-induced atom transfer radical polymerization and used as water-soluble monomer to prepare polyester separation layer on porous substrates through interfacial polymerization with trimelanoyl chloride. The obtained POSS-centered polyester membrane exhibits a high dye removal rate exceeding 99 %, and it can realize the screening of dye molecules with different molecular weight and different charge. Notably, the membrane demonstrates excellent chlorine resistance, maintaining effective separation efficiency after exposure to sodium hypochlorite solutions at concentrations of 10 000 ppm for 96 h and 1000 ppm for 7 days. It is worth noting that the membrane showed high anti-fouling performance. This method provides a useful guideline for the development of chlorine-resistant and anti-fouling separation membranes.

Occurrence of chlorine-resistant Pseudomonas aeruginosa in hospital water systems: threat of waterborne infections for patients

BackgroundSeveral healthcare-associated infection outbreaks have been caused by waterborne Pseudomonas aeruginosa exhibiting its ability to colonize water systems and resist conventional chlorine treatment. This study aims to investigate the occurrence of Pseudomonas aeruginosa in hospital drinking water systems and the antimicrobial resistance profiles (antibiotic and chlorine resistance) of isolated strains.MethodsWe investigated the presence of Pseudomonas aeruginosa in water and biofilms developed in nine hospital water systems (n = 192) using culture-based and molecular methods. We further assessed the survival of isolated strains after exposure to 0.5 and 1.5 ppm concentrations of chlorine. The profile of antibiotic resistance and presence of antibiotic resistance genes in isolated strains were also investigated.ResultsUsing direct PCR method, Pseudomonas aeruginosa was detected in 22% (21/96) of water and 28% (27/96) of biofilm samples. However, culturable Pseudomonas aeruginosa was isolated from 14 samples. Most of P. aeruginosa isolates (86%) were resistant to at least one antibiotic (mainly β-lactams), with 50% demonstrating multidrug resistance. Moreover, three isolates harbored intI1 gene and two isolates contained blaOXA−24,blaOXA−48, and blaOXA−58‌ genes. Experiments with chlorine disinfection revealed that all tested Pseudomonas aeruginosa strains were resistant to a 0.5 ppm concentration. However, when exposed to a 1.5 ppm concentration of chlorine for 30 min, 60% of the strains were eliminated. Interestingly, all chlorine-resistant bacteria that survived at 30-minute exposure to 1.5 ppm chlorine were found to harbor the intI1 gene.ConclusionsThe detection of antimicrobial resistant Pseudomonas aeruginosa in hospital water systems raises concerns about the potential for infections among hospitalized patients. The implementation of advanced mitigation measures and targeted disinfection methods should be considered to tackle the evolving challenges within hospital water systems.

A Novel Method for Increasing the Concrete Resistance to Chloride Ions Erosion

Concrete structures generally play an important role in the infrastructure construction. The corrosion of reinforcing steels in concrete structures is one of the main causes of the degradation and reduction of their service life, especially when they are exposed to marine environment or de-icing salts. An understanding of the process of chloride transportation in concrete is of great importance for engineers to predict the service life of concrete structures. Therefore, we synthesized corrosion inhibitor for improving the chlorine resistance of concrete.

Comparing durability and compressive strength predictions of hyperoptimized random forests and artificial neural networks on a small dataset of concrete containing nano SiO2 and RHA

Through the increasing use of supplementary cementitious materials, the properties of concrete have taken on increased significance in a design code. Using reliable prediction models based on a small data set for the mechanical properties and durability of concrete can reduce the number of trial batches and experiments needed to produce useful design data in the laboratory, reducing time as well as resources. In this study, we investigate how the properties of water penetration, chlorine resistance, and compressive strength can be predicted by polynomial regression (PR), random forest (RF) regression, and artificial neural networks (ANNs) based on the input values of density, workability, and the constituent amount of rice husk ash, cement, and nano SiO 2 . We vary the training data used and test the coefficient of determination ( R 2 score) on the remaining data as a test set to measure predictive capability. We show that RFs and ANNs outperform PR in all settings and have unambiguously extrapolating properties when hyperparameter optimization is designed for this purpose. Remarkably, we obtain R 2 scores on the test data of 0.858 − 0.990 for RFs and 0.825 − 0.985 for ANNs.

Coordination Environment and Distance Optimization of Dual Single Atoms on Fluorine‐Doped Carbon Nanotubes for Chlorine Evolution Reaction

AbstractThe chlorine evolution reaction (CER) is a crucial anode reaction in the chlor‐alkali industrial process. Precious metal‐based dimensionally stable anodes (DSA) are commonly used as catalysts for CER but are constrained by their high cost and low selectivity. Herein, a Pt dual singe‐atom catalyst (DSAC) dispersed on fluorine‐doped carbon nanotubes (F‐CNTs) is designed for an efficient and robust CER process. The prepared Pt DSAC demonstrates excellent CER activity with a low overpotential of 21 mV to achieve a current density of 10 mA cm−2 and a remarkable mass activity of 3802.6 A gpt−1 at an overpotential around 30 mV, outperforming those of commercial DSA and Pt single‐atom catalyst. The excellent CER performance of Pt DSAC is attributed to the high atomic utilization and improved intrinsic activity. Notably, introducing fluorine atoms on CNTs increases the oxidation and chlorination resistance of Pt DSAC, and reduces the demetalization ratio of Pt atoms, resulting in excellent long‐term CER stability. Theoretical calculations reveal that several Pt DSAC configurations with optimized first‐shell ligands and interatomic distance display lower energy barriers for Cl intermediates generation and weaker ionic Pt−Cl bond interaction, which are favorable for the CER process.

Investigation on the microstructure, mechanical properties and chlorine resistance of fine aluminum alloy wires

Wire bonding is a fundamental and mature technology in semiconductor packaging process, primarily using materials such as gold, silver, aluminum, and copper for the wires. To address application limitations of aluminum wires, such as low electromigration resistance and limited ductility, techniques including to enhance alloying (with Zn and Si), heat treatment, and surface treatment are employed to enhance the performance of aluminum alloy wires and broaden their application value. This study selects Al-3Zn-0.3Si (AZS303) and Al-7Zn-0.3Si (AZS703), with AZS303 undergoing gold plating to produce AC-AZS303 wires. Various high-temperature heat treatments are applied, verifying that under 400 °C conditions, the AZS series aluminum alloy wires exhibit grain growth and form single-crystal equiaxed grain structures, resulting in stable mechanical properties and excellent electrical performance. Additionally, the AC-AZS303 wires optimize resistance values through gold layer diffusion induced by the electrothermal effect.Chlorine experiments indicates that the gold plating on AC-AZS303 can't enhance the aluminum wire's resistance to chlorine corrosion. However, the alloying effect of zine and silicon elements imparts excellent chlorine corrosion resistance to the Al-Zn-Si wires. This study of bonding properties examines the bond strength and observes the bonded area of Al-Zn-Si wires after bonding. It is noted that the H400-AZS303 wire exhibits the best bond strength and bonding area, demonstrating good bonding with the substrate.

Bis-tris-based polyester nanofiltration membranes fabricated via one-step interfacial polymerization for desalination

To obtain high-performance polyester (PE) nanofiltration (NF) membranes for desalination, most PE NF membranes are fabricated with high aqueous monomer concentration, or high reaction temperature, or long reaction time. The interfacial polymerization (IP) reaction rate between hydroxyl groups and acyl chloride groups is promoted but the cost of membrane fabrication is also increased. In this work, Bis-tris (bis(2-hydroxyethyl)-amino-tris(hydroxymethyl)methane) with rich hydroxyl groups is first utilized as an aqueous monomer to fabricate PE membranes under conventional IP conditions. The fabricated Bis-tris PE membranes feature strong hydrophilicity, excellent electronegativity, and ultra-thin selective layers, which are conducive to improving desalination performance. The optimized Bis-tris PE membrane shows excellent water permeance of 22.5 L m−2 h−1 bar−1 and a satisfactory Na2SO4 rejection of 96.9 %. Additionally, the Bis-tris PE membrane displays superior long-term stability and chlorine resistance under 96 h cross-flow filtration. This research enlightens the promising potential of Bis-tris as a novel and economic aqueous monomer for the fabrication of high-performance PE NF membranes.

Effect of antibiotics and antibiotic by-products on the chlorine resistance of biofilms in drinking water distribution systems

This study investigated the effects of tetracycline (TC) and sulfadiazine (SD), along with their degradation products, on biofilm chlorine resistance. The results showed that low concentrations of antibiotics and their degradation products promoted biofilm formation on tube surfaces and increased resistance to chlorine. There was a positive correlation between antibiotic levels, degradation products, and biofilm chlorine resistance within a specific concentration range. SD had a more significant impact on biofilm chlorine resistance compared to TC. The presence of both antibiotics and their degradation products in water led to an increase in biofilm chlorine resistance, especially when combined with 0.3 mg/L sodium hypochlorite. The study shows a positive association between antibiotic and degradation product concentrations and the biofilms' improved chlorine resistance, a phenomenon that could have major consequences for water treatment efforts. Additionally, higher concentrations of antibiotics and their degradation products were associated with reduced biodiversity within the biofilm. Overall, the findings suggest that the presence of antibiotics and their degradation products can influence biofilm formation, alter bacterial species composition, and enhance biofilm resistance to chlorine in drinking water distribution systems. This fresh perspective on the relationship between pharmaceutical residues and microbial communities in water systems could transform our approach to assuring water safety and combatting antimicrobial resistance.

Next generation desalination membrane with exceptional chlorine resistance

Next generation desalination membrane with exceptional chlorine resistance

Polyvinyl alcohol-modified β-cyclodextrin incorporated forward osmosis membranes with good chlorine resistance

The applications of β-cyclodextrin (β-CD) in chlorine-resistant membranes have always faced the challenge of agglomeration at high concentrations. In this study, polyvinyl alcohol (PVA) modified β-CD was used as a monomer to prepare forward osmosis (FO) membranes with high chlorine resistance. Scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR), automated contact angle meter (CAM), electrodynamic analyzer (EA), X-ray photoelectron spectroscopy (XPS), and true color confocal microscopy (CSM) have been used to characterize the physicochemical properties of the FO membrane. The agglomerated β-CD affected the formation of the selective layer, resulting in reduced water fluxes ranging from 12.4 L m−2 h−1 to 1.75 L m−2 h−1. The modified TFC-PVA-β-CD FO membrane had a complete, defect-free selective layer, and water flux of 16.75 L m−2 h−1 at 1 M NaCl as a draw solution. FTIR spectra showed that the absorption peak intensity of the carbonyl (CO) group generated from β-CD and 1,3,5-Benzene tricarbonyl trichloride (TMC) increased after PVA modification. After 6 hours of chlorination, the reverse salt flux of the thin film composite (TFC) FO membranes abided by the following order: TFC (80.35 g m−2 h−1) > TFC-β-CD (60.95 g m−2 h−1) > TFC-PVA-β-CD (12.45 g m−2 h−1). The results indicated that the PVA effectively promotes uniform dispersion of β-CD. More chlorine-resistant ester bonds (-COO-) were formed in the TFC-PVA-β-CD FO membrane, so it possessed good chlorine resistance. This study provides a green, simple, and environmentally economical method for the preparation of chlorine-resistant FO membranes.

Coordination Environment and Distance Optimization of Dual Single Atoms on Fluorine-Doped Carbon Nanotubes for Chlorine Evolution Reaction.

The chlorine evolution reaction (CER) is a crucial anode reaction in the chlor-alkali industrial process. Precious metal-based dimensionally stable anodes (DSAs) are commonly used as catalysts for CER but are constrained by their high cost and low selectivity. Herein, a Pt dual singe-atom catalyst (DSAC) dispersed on fluorine-doped carbon nanotubes (F-CNTs) is designed for an efficient and robust CER process. The prepared Pt DSAC demonstrates excellent CER activity with a low overpotential of 21 mV to achieve a current density of 10 mA cm-2 and a remarkable mass activity of 3802.6 A gpt-1 at an overpotential around 30 mV, outperforming those of commercial DSA and Pt single-atom catalysts. The excellent CER performance of Pt DSAC is attributed to the high atomic utilization and improved intrinsic activity. Notably, introducing fluorine atoms on CNTs increases the oxidation and chlorination resistance of Pt DSAC, and reduces the demetalization ratio of Pt atoms, resulting in excellent long-term CER stability. Theoretical calculations reveal that several Pt DSAC configurations with optimized first-shell ligands and interatomic distance display lower energy barriers for Cl intermediates generation and weaker ionic Pt-Cl bond interaction, which are favorable for the CER process.

Terminal conversion of polyamide membranes by homologous monomer vapors for chlorine-resistant desalination

Water scarcity is a global challenge and severely threatens human development. Membrane desalination shows great potential for producing freshwater from saltwater to alleviate this crisis. However, the dominating polyamide membranes suffer from the issue of poor chlorine resistance, which cause performance deterioration and shortens membrane lifespan. In this study, we report a concept of terminal conversion to design high-performance, antifouling, and especially chlorine-resistant polyamide desalination membranes. This amino-to-carboxyl conversion of commercial membranes can be simply performed by controllable and scalable chemical vapor deposition through exposure in homologous monomer vapor and hydrolysis of unreacted acyl chloride groups. We demonstrate that this conversion not only adjust the electronegativity and hydrophilicity of membranes to boost fouling resistance and reverse osmosis performance, but also tune the reactivity and electron cloud distribution of polyamide networks to restrain chlorine accessibility and substantially improve anti-chlorination property. After extreme chlorination for 240000 ppm h, the resultant membranes show limited rejection decline of only 7.2 %. For high-salinity (35000 ppm) and high-pressure (38 bar) desalination, the modified membranes before and after chlorination for 144000 ppm h still exhibit rejection of 94.5 % and 90.0 % and flux of 75.2 and 71.4 L m−2 h−1, respectively, which are much better than those of the pristine membranes (89.6 % and 63.5 %, and 64.2 and 57.5 L m−2 h−1). Our findings pave an alternative mechanism and strategy to reconstruct polyamide membranes for efficient water desalination.

Preparation of polyethylene based composite nanofiltration membrane and its application in removal of heavy metals for water purification

The commercial polyethylene (PE) battery separator is well-suited as support for nanofiltration owing to its thickness of 7 um, high porosity, and strong mechanical properties. A new polyethylene based thin-film composite membrane was fabricated on the catechol/polyethyleneimine (CCh/PEI) modified PE support by pre-diffusion interfacial polymerization between piperazine (PIP) and trimesoyl chloride (TMC). By regulating the properties of the CCh/PEI layer and the PIP to influence the diffusion of PIP, a distinct worm-like structure in the polyamide (PA) layer was found, which provides more water penetration sites. After grafting melamine on the surface of PA layer, the TFC membrane exhibited outstanding chlorine resistance and the permeability of 12.5 L·m−2·h−1·bar−1 with the Mg2+ rejection of 94.5 %. Due to its small pore size, strong positively charged, and high adsorption capacity, the TFC membrane showed high rejection of heavy metal ions through pore size sieving, Donnan effect and adsorption. Therefore, it has great potential for water purification from heavy metal ions.

Optimization of mass transfer-enhanced chlorine-resistant crosslinked PVA composite membranes for pervaporation desalination

Pervaporation (PV) is characterised by good hydrophilicity and antifouling properties. However, it is still unavoidable to need cleaning during long-term operation. Sodium hypochlorite (NaClO) is a commonly used purifying agent for organic pollutants, but it may cause damage to the polymer membrane. In this study, a grafting method was proposed to enhance the chlorine resistance and water permeability of membrane composite polyvinyl alcohol (PVA) pervaporation membrane. Modified PVA (SPVA) was prepared by grafting 5-sulfosalicylic acid (SSA) to improve the hydrophilicity of the membrane using the sulfonic acid group on SSA. SPVA-FA/PTFE composite membranes were prepared by using perfluoroglutaric acid (PFGA) as crosslinking agent to improve the chlorine resistance of the membranes by utilising the C-F chain contained therein. The water flux was 120.38 ± 1.72 kg/(m2·h), which was 84.2 % higher than that before grafting, when tested at 70 °C and 3.5 wt% NaCl. The chlorine resistance of SPVA-PFGA/PTFE composite membrane was tested in 2000 ppm (pH = 12) NaClO solution for 480 h, and the salt rejection remained above 99.93 %. When desalinating 20 wt% NaCl at 70 °C, the water flux of SPVA-PFGA/PTFE membrane is 51.95 ± 0.6 kg/(m2·h), which has the potential to treat high concentration brine.