Membrane Adsorption Research Articles

Viscoelastic Properties of Electrospray‐Deposited Polymer Shells via Quartz Crystal Microbalance With Dissipation (QCM‐D)

AbstractMultilayer polymer films are extensively used in multiphase separation. Electrospray deposition (ESD) is an important technique for fabricating such films with tunable morphology. Viscoelastic properties of polystyrene (PS) nanoshell coatings produced by ESD on gold and spin‐coated PS surfaces are evaluated using Quartz Crystal Microbalance with Dissipation (QCM‐D). The thickness of PS films on gold increases with flow rate from ∼200 nm at 0.5 to ∼400 nm at 1.5 mL h−1, accompanied by an order‐of‐magnitude increase in dissipation due to larger particle sizes from shorter droplet flight times. This effect is absent on spin–coated PS films, suggesting the onset of the self‐limiting effect of charges. Although the shear moduli for ESD films calculated from Voigt models is only 0.08%–0.20% of the bulk PS modulus, the stiffness ratio of spray‐coated PS to a single shell is (5.00–13.3) × 103 m−1, due to shell–shell and shell–substrate interactions. These are novel results related to the interparticle friction obtained using QCM‐D for the first time. This work demonstrates that mechanical properties of particulate viscoelastic films with potential applications in high surface area sensors, such as size‐selective membranes for protein or electrolyte adsorption, can be evalauted by QCM‐D with nanograms of material.

Selective separation and recovery of Co(II) and Ni(II) from lithium-ion battery using Cyanex 272 adsorptive membrane

Selective separation and recovery of Co(II) and Ni(II) from lithium-ion battery using Cyanex 272 adsorptive membrane

Moment analysis method for the determination of permeation kinetics of coumarin at lipid bilayers of liposomes by using capillary electrophoresis.

A method was developed for studying mass transfer kinetics at lipid bilayers of liposomes. Elution peaks of coumarin were measured by liposome electrokinetic chromatography (LEKC). Four types of phospholipids having different alkyl chains were used for preparing liposomes, which were used as pseudo-stationary phases in LEKC systems. Rate constants of permeation across lipid bilayers of liposomes or of adsorption at lipid membranes were determined by analyzing the first absolute and second central moments of the elution peaks measured by LEKC. The rate constants of permeation or adsorption tend to decrease with an increase in the carbon number of the alkyl chains of phospholipids. It was demonstrated that the moment analysis of elution peak profiles measured by LEKC is effective for determining lipid membrane permeability or adsorption kinetics. Compared with other conventional techniques, the method has some advantages for studying mass transfer kinetics at lipid bilayers. Solute permeation across or solute adsorption at real lipid bilayers of liposomes is analyzed. The principle of the method is the analysis of separation behavior in LEKC, which is different from that of the other ones. It is expected that the method contributes to the kinetic study of mass transfer at lipid bilayers from various perspectives.

Aromatic Amine-Supported N-Functionalization of Nanoscale-Thick Graphene Oxide Membranes for Preferential Adsorption of Strontium Ions from Aqueous Solutions

Aromatic Amine-Supported N-Functionalization of Nanoscale-Thick Graphene Oxide Membranes for Preferential Adsorption of Strontium Ions from Aqueous Solutions

Development of two-dimensional amyloid fibril/carboxymethyl cellulose hybrid membranes for effective adsorption of hexavalent chromium

Amyloid fibrils (AFs) are protein aggregates with highly ordered fibrillar structures and can be formed via self-assembly of proteins under appropriate conditions. Owing to the unique properties of AFs, e.g., high surface-to-volume ratio and versatile functional groups, they offer abundant binding sites for the efficient adsorption of hexavalent chromium (Cr(VI)). This study was aimed at examining the performance of two-dimensional AF-based hybrid membranes for adsorbing Cr(VI). First, AF/carboxymethyl cellulose (AF/CMC) hybrid membranes were synthesized via chemical crosslinking coupled with phase inversion, followed by investigating the synthesis mechanism using Fourier transform infrared spectroscopy. Our results revealed that the surface microstructures and mechanical properties of the hybrid membranes could be affected by the AF:CMC mass ratio of the membrane. The porosity and ζ-potential of hybrid membranes were found to be dependent on both pH value and membrane composition. Analyses of the kinetics and thermodynamic behavior of Cr(VI) adsorption on the AF/CMC hybrid membranes revealed that the initial adsorption rate and maximum adsorption capacity were determined to be ∼149.20 mg g–1 h–1 and ∼311.11 mg g–1, respectively. The Cr(VI) removal percentage of hybrid membrane with high CMC content was found to remain at >75 % after five successive adsorption-desorption cycles. Finally, the mechanism and interactions involved in the adsorption of Cr(VI) on the hybrid membrane were further investigated via thermodynamic analysis and X-ray photoelectron spectroscopy. This study provides an excellent example of harnessing AF-based membranes in water remediation, highlighting the potential of AF-based hybrid materials for wastewater treatment applications.

Membrane Adsorption Enhances Translocation of Antimicrobial Peptide Buforin 2.

Despite ongoing research on antimicrobial peptides (AMPs) and cell-penetrating peptides (CPPs), their precise translocation mechanism remains elusive. This includes Buforin 2 (BF2), a well-known AMP, for which spontaneous translocation across the membrane has been proposed but a high barrier has been calculated. Here, we used computer simulations to investigate the effect of a nonequilibrium situation where the peptides are adsorbed on one side of the lipid bilayer, mimicking experimental conditions. We demonstrated that the asymmetric membrane adsorption of BF2 enhances its translocation across the lipid bilayer by lowering the energy barrier by tens of kJ mol-1. We showed that asymmetric membrane adsorption also reduced the free energy barrier of lipid flip-flop but remained unlikely even at BF2 surface saturation. These results provide insight into the driving forces behind membrane translocation of cell-penetrating peptides in nonequilibrium conditions, mimicking experiments.

Adsorptive membrane separation for eco-friendly decontamination of chlorpyrifos via biochar-impregnated cellulose acetate mixed matrix membrane.

In this work, the phase inversion approach is used to synthesize a blended mixed matrix membrane from cellulose acetate polymer and sugarcane bagasse biochar. The experiments were carried out to estimate the extent of chlorpyrifos (CPS) pesticide removal. The results showed that the removal rate was more than 99% in making the filtered water suitable enough for domestic use. The physical and functional characteristics of the membranes, such as permeability, and contact angle were identified. The changes in the membrane characteristics were observed using scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction both before and after the experimental trials. Experiments were conducted to assess not only the rejection characteristics of CPS, as a function feed concentration, but also the effect co-ions on the rejection used to analyze the composition both before and after filtration. The effects of initial CPS concentration, biochar loading, and co-ions on the membrane were investigated. The membranes showed contact angles between 70° and 97° and a permeability between 0.25 × 1010 m Pa-1 s-1 and 0.31 × 1010 m Pa-1 s-1. The effective removal of CPS from the contaminated aqueous stream was attributed to a combination of adsorptive uptake and membrane-based separation. CPS was found to get adsorbed onto the membrane matrix through an intraparticle diffusion mechanism along with an irreversible monolayer adsorption. The membrane-solute adsorptive interaction was represented by Langmuir isotherm and intraparticle diffusion models with a maximum adsorption capacity of 192.3 mg g-1. The findings indicated the efficacy of biochar-cellulose acetate mixed matrix membrane for sustainable and eco-friendly treatment of chlorpyrifoscontaminated water.

Facile Fabrication of Zeolitic Imidazolate Framework-8@Regenerated Cellulose Nanofibrous Membranes for Effective Adsorption of Tetracycline Hydrochloride.

The excessive utilization of antimicrobials in humans and animals has resulted in considerable environmental contamination, necessitating the development of high-performance antibiotic adsorption media. A significant challenge is the development of composite nanofibrous materials that are both beneficial and easy to fabricate, with the aim of improving adsorption capacity. Herein, a new kind of zeolitic imidazolate framework-8 (ZIF-8)-modified regenerated cellulose nanofibrous membrane (ZIF-8@RC NFM) was designed and fabricated by combining electrospinning and in situ surface modification technologies. Benefiting from its favorable surface wettability, enhanced tensile strength, interconnected porous structure, and relatively large specific surface area, the resulting ZIF-8@RC NFMs exhibit a relatively high adsorption capacity for tetracycline hydrochloride (TCH) of 105 mg g-1 within 3 h. Moreover, a Langmuir isotherm model and a pseudo-second-order model have been demonstrated to be more appropriate for the description of the TCH adsorption process of ZIF-8@RC-3 NFMs. Additionally, this composite fibrous material could keep a relatively stable adsorption capability under various ionic strengths. The successful fabrication of the novel ZIF-8@RC NFMs may shed light on the further development of wastewater adsorption treatment materials.

An Overview of Optical Sensing of Copper and its Removal by Different Techniques

: The identification of heavy metals by sensing technologies is a crucial area of study since these metals are present in the environment and are hazardous. The in-depth analyses of the probes' structures and sensing capabilities improve our understanding of how to design and develop probes for the same metal in the future. The third most common metal ion and trace element, copper (Cu2+), is essential to all living things and is involved in several activities. However, different diseases are caused by excess or deficiency of Cu2+ ions, depending on what the cell requires. For all of these reasons, optical sensors have concentrated on quick, highly sensitive, and selective real-time detection of Cu2+ ions. Fluorescence in the refractive index-adsorption from the interactions between light and matter can be measured using optical sensors. Furthermore, due to their strong advantages which include real-time detection, simplicity and naked eye recognition, low cost, high specificity against analytes, quick reaction, and the requirement for less complex equipment during analysis they have attracted a lot of attention in recent years. In this review, we covered many fluoro and chemosensors for the detection of copper, along with their sensing parameters in various mediums and thorough structural analyses. This review also covers the extraction of copper from the aqueous medium. The use of membrane processes, adsorption, and electrocoagulation is examined, and the difficulties associated with their application have been presented.

Study on corrosion inhibition of carbon steel by imidazolylium-based ionic liquids in chlorine dioxide water disinfection

Chlorine dioxide (ClO2), recognized for its high efficiency, broad-spectrum capabilities, and safety, is extensively utilized in water disinfection processes. Possessing strong oxidizing properties, prolonged exposure to ClO2 can lead to irreversible corrosion of metals. To mitigate the ClO2-induced corrosion on steel, the corrosion inhibition performance and underlying mechanism of BMIMAc and BMIMBr on 20 steel and Q235 steel in ClO2 solutions ranging from 2.5 to 10 mg/L is systematically studied by static weightlessness experiments, potentiodynamic polarization curve experiments, SEM, EDS, DFT calculations, and MD simulation. The findings demonstrate that both ionic liquids significantly impede corrosion, where BMIMAc outperforms BMIMBr in terms of corrosion inhibition efficacy. These inhibitors exhibit effective adsorption onto the carbon steel surface, conforming to the Langmuir isotherm model. Both ionic liquids are cathodic inhibitors. They can adsorb on the metal surface in an approximately parallel manner and their imidazole ring can form a coordination bond with the metal, leading to the formation of an adsorbent membrane that prevents further contact of the metal with ClO2, thus reducing the degree of oxidation and retarding the corrosion process.

Arsenic removal from contaminated water using adsorptive electrospun nanofibrous membrane of polyacrylonitrile/organoclay

AbstractAdsorptive nanofiber electrospun membranes (ANEMs) show promise for heavy metal removal, particularly in dilute solutions. Nanofibrous polyacrylonitrile (PAN) membranes incorporating Cloisite 20A (C20) organoclay were fabricated via electrospinning for As(V) removal. The impact of C20 on structural properties and As(V) removal efficiency of the nanofiber membranes was investigated. The results indicated that the PAN‐C20 membranes morphology was uniform, with fiber diameters mostly falling within the 100–300 nm range. Incorporation of C20, especially in an exfoliated structure, led to increased hydrophilicity, mechanical strength, and roughness of the membranes. Batch adsorption results revealed that the adding C20 up to 1.5 wt.% significantly enhanced adsorption capacity due to the higher concentration and proper C20 dispersion. Dynamic filtration showed that the PAN‐C20(1.0) membrane achieved over 90% As(V) removal efficiency for 960 min and demonstrated excellent regeneration ability.Highlights Cloisite 20A organoclay was incorporated into PAN by electrospinning to prepare adsorptive membrane. Adsorptive membranes were used for As(V) removal from water. Type of Cloisite 20A dispersion in PAN in dynamic filtration was more important than in static adsorption PAN‐C20‐1.0 with exfoliated structure showed higher removal efficiency than PAN‐C20‐1.0 with intercalated structure. PAN‐C20‐1.0 membrane was usable for multiple adsorption–desorption cycles.

Lanthanum hydroxide@cellulose membranes with tunable pore sizes for selective removal of dyes with the same charges

Adsorptive membranes for the efficient separation of dyes with the same charges are quite desirable. Herein, a novel membrane of lanthanum hydroxide/cellulose hydrogel coated filter paper (LC) was prepared through a facile strategy of dip-coating followed by freeze-shaping. With the aid of cellulose gel, the generated La(OH)3 achieved fine dispersion. In addition, the pore size of LC membrane could be regulated by altering the cellulose concentration or the lanthanum chloride dosage, which was crucial for its water flux. In particular, the obtained membrane possessed a high water flux (128.4 L m−2 h−1) and a high dye rejection (97.2 %) for anionic Congo red (CR) only driven by the gravity, which outperformed many previously reported membranes. More intriguingly, its dye rejection for anionic methyl orange (MO) was only 0.9 %, exhibiting high selectivity for dyes with the same charges. Single-solute adsorption experiments indicated that the CR adsorption on the membrane was best fitted by the pseudo-first-order kinetic model, and it followed the Langmuir monolayer adsorption mechanism.

Fabrication of mixed matrix membranes based on PVDF matrix and ZrT-1-NH2 filler for efficient adsorptive removal of Orange G

Adsorption membranes have become a hot spot for wastewater treatment in recent years. Due to the lack of active sites in traditional inert materials such as polyvinylidene fluoride (PVDF) membranes, it is difficult to bind pollutants in water with high affinity. Therefore, in this study, ZrT-1-NH2/PVDF mixed matrix membranes (MMMs) were prepared by combining an amino-functionalized Zr-based metal–organic cage (ZrT-1-NH2) with a polymer substrate via non-solvent-induced phase separation method for the efficient removal of Orange G (OG) from water. This method has many advantages such as simplicity in operation, high applicability, controllable MOFs loading. The structural characteristics and adsorption properties and of MMMs were also investigated through a series of characterizations and experiments. The result shows that in a 100 mL OG solution with an initial concentration of 50 mg/L and pH=3, M60 exhibited significant adsorption capacity, the removal efficiency reached 97.23 %, with an adsorption capacity of 64.18 mg/g, which is much higher than the pristine PVDF membrane. It is mainly attributed to electrostatic interactions and hydrogen bonding interactions between ZrT-1-NH2 and OG molecules. This is consistent with the DFT calculations. The introduction of ZrT-1-NH2 filler improves the performance of PVDF membranes and expands their potential applications.

Bioinspired Microgel-Loaded Smart Membrane Filtration with the Thermo- and Ion-Dual Responsive Water Gate for Selective Lead(II) Separation.

Lead (Pb2+) is a ubiquitous pollutant. Membrane filtration represents one of the most common water treatment methods, but nanofiltration and ultrafiltration require high transmembrane pressure, while microfiltration has larger pore sizes than ions, making them unfavorable for direct ion removal at low cost. Selective and direct separation of Pb2+ via membrane filtration at high efficiency without sacrificing the flux of clean water still remains challenging. Herein, inspired by the Pb2+-tolerable oleander that enriches and prevents Pb2+ in roots from permeating the plant body, a smart Pb2+-adsorptive filtration membrane with a temperature- and ion-tunable water gate was prepared by loading dual-responsive poly(N-isopropylacrylamido-co-acrylamido-benzo-18-crown-6) (PNB-5-20) microgels onto a commercial membrane. The PNB-5-20 microgel exhibits pronounced temperature-responsive swelling/deswelling (hydrodynamic diameter, 650-330 nm) with a volume phase transition temperature (VPTT) at ∼33 °C. Moreover, the microgel shows a high Pb2+-adsorption capacity (qmax, 85.4 mg/g) and good selectivity (distribution coefficient Kd ∼ 1000 mL/g) thanks to its complexation with the crown ether, as well as good Pb2+ responsiveness, having the VPTT positively shifted to 40 °C in the presence of Pb2+ with enhanced swelling behaviors. Functionalized with PNB-5-20, the smart membrane integrates Pb2+ detection, adsorption, and tunable water drainage in a single device. The membrane selectively recognizes Pb2+ in the polluted water with the gates in membrane pores switching from "open" to "closed", intercepting and adsorbing Pb2+ with water permeation reduced. Once purified, the gates can be "re-opened" by increasing the temperature. Construction of such an intelligent membrane filtration device with a tunable water gate and excellent Pb2+ recognition and adsorption performance will greatly simplify the remediation of Pb2+-polluted water.

Polysulfone membranes decorated with Fe–Mn binary oxide nanoparticles and polydopamine for enhanced arsenate/arsenite adsorptive removal

Arsenic contamination of water is a global environmental concern, and membrane technology combined with nanotechnology contributes to more efficient removal of arsenic. In this study, Fe–Mn oxide (FM), Polydopamine (PDA), and PDA-modified FM (PFM) were incorporated into polysulfone (PSF) to prepare adsorption membranes (PFMP) for arsenic removal. The prepared nanoparticles and membranes were characterized using TEM, SEM, FTIR, TGA, contact angle, and pure water flux. The introduction of particles enhanced the hydrophilicity of the membranes and significantly enhanced the pure water flux of the membranes. Adsorption experiments indicated that the PFMP membrane exhibited the best arsenic removal performance, with maximum adsorption capacities for As(III) and As(V) were 11.57 mg/g and 12.39 mg/g, respectively. The Langmuir model fitted the adsorption isotherms well, and the kinetics followed the pseudo-second-order model. The filtration experiment revealed that the PFMP membrane was capable of reducing As(III) solution (915 L/m2) and As(V) solution (1075 L/m2) from a concentration of 100 μg/L to the safe limit of As (＜10 μg/L). The As-loaded membrane was regenerated using NaOH solution (pH = 11), and the filtration experiment was repeated. FTIR and XPS demonstrated that the mechanism of the reaction between the membrane and arsenic was ligand exchange, where the arsenic ions were bonded to the oxygen ions to form Mn–O–As and Fe–O–As.

Construction of Imprinted Bacterial Cellulose Composite Membranes for Selective Adsorption of Cesium from Low Concentration Radioactive Wastewater

Construction of Imprinted Bacterial Cellulose Composite Membranes for Selective Adsorption of Cesium from Low Concentration Radioactive Wastewater

Photocatalytic nanohybrid UV-light-driven PVDF/GO-NiFe@SiO2 membrane coupled with bentonite adsorption and ozonation process for a sustainable textile wastewater treatment

The textile industries face significant environmental challenges due to the presence of complex pollutant dyes in its wastewater, making it one of the world's major sources of industrial water pollution. Numerous studies have been employed to overcome this problem, including physical, chemical, and biological treatments. However, most of those methods still suffered to achieve higher dye removal performance. This study provides new insight regarding textile wastewater treatment containing indigo red as the main colorant by carrying out a hybrid process combining bentonite adsorption, ozonation, and photocatalytic membrane filtration. For the membrane, we propose a modified polyvinylidene fluoride (PVDF) membrane incorporated with graphene oxide (GO) and nickel-iron doped silica (NiFe@SiO2) photocatalyst, which is named PVDF/GO-NiFe@SiO2 membrane. The membrane was employed under different sets of filtrations (dark and under ultraviolet irradiation) to treat natural dye wastewater from textile industry effluent. Further improvement was achieved when UV light irradiation was subjected to the process. This sequential adsorption-ozonation-membrane process under UV exposure exhibited improved dye removal from 55.11 % to 97.22 %. The results show that the proposed hybrid process successfully improved the membranes' antifouling behavior, thus boosting the membranes' performance and durability. From a broader perspective, our work promotes new insights for the integration of other physical, chemical, and biological treatment methods to improve the performance and durability of membrane-based processes, particularly for dye wastewater treatment.

High-volume hemofiltration does not protect human kidney endothelial and tubular epithelial cells from septic plasma-induced injury

High volume hemofiltration (HVHF) could remove from plasma inflammatory mediators involved in sepsis-associated acute kidney injury (SA-AKI). The IVOIRE trial did not show improvements of outcome and organ dysfunction using HVHF. The aim of this study was to evaluate in vitro the biological effects of plasma of patients treated by HVHF or standard volume hemofiltration (SVHF). We evaluated leukocyte adhesion, apoptosis and functional alterations of endothelial cells (EC) and tubular epithelial cells (TEC). In vitro data were correlated with plasma levels of TNF-α, Fas-Ligand (FasL), CD40-Ligand (CD40L), von Willebrand Factor (vWF) and endothelial-derived microparticles. An experimental model of in vitro hemofiltration using LPS-activated blood was established to assess cytokine mass adsorption during HVHF or SVHF. Plasma concentrations of TNF-ɑ, FasL, CD40L and von Willebrand Factor (vWF) were elevated at the start (d1h0) of both HVHF and SVHF, significantly decreased after 6 h (d1h6), remained stable after 12 h (d1h12) and then newly increased at 48 h (d3h0). Plasma levels of all these molecules were similar between HVHF- and SVHF-treated patients at all time points considered. In addition, the levels of endothelial microparticles remained always elevated, suggesting the presence of a persistent microvascular injury. Plasma from septic patients induced leukocyte adhesion on EC and TEC through up-regulation of adhesion receptors. Moreover, on EC, septic plasma induced a cytotoxic and anti-angiogenic effect. On TEC, septic plasma exerted a direct pro-apoptotic effect via Fas up-regulation and caspase activation, loss of polarity, altered expression of megalin and tight junction molecules with an impaired ability to internalize albumin. The inhibition of plasma-induced cell injury was concomitant to the decrease of TNF-α, Fas-Ligand and CD40-Ligand levels. The protective effect of both HVHF and SVHF was time-limited, since a further increase of circulating mediators and plasma-induced cell injury was observed after 48 h (d3h0). No significant difference of EC/TEC damage were observed using HVHF- or SVHF-treated plasma. The in vitro hemofiltration model confirmed the absence of a significant modulation of cytokine adsorption between HVHF and SVHF. In comparison to SVHF, HVHF did not increase inflammatory cytokine clearance and did not reverse the detrimental effects of septic plasma-induced EC and TEC injury. Further studies using adsorptive membranes are needed to evaluate the potential role of high dose convective therapies in the limitation of the harmful activity of plasma soluble factors involved in SA-AKI.Trial registration IVOIRE randomized clinical trial; ClinicalTrials.gov (NCT00241228) (18/10/2005).

Membrane-based technologies for removing emerging contaminants in urban water systems: Limitations, successes, and future improvements

Emerging contaminants (ECs) have been continuously discovered in recent years, posing high risks to human health and environmental safety. Due to their characteristics, such as environmental persistence and bioaccumulation, ECs have severe and often hidden hazards, necessitating effective control measures. Membrane-based technologies possess satisfactory feasibility in the treatment of ECs, which are considered green, efficient, and economically beneficial. Membrane technologies such as membrane separation and membrane bioreactor (MBR) treatment can efficiently remove some ECs. With the rapid development of materials science, membrane-based coupled technologies such as catalytic membranes and adsorption membranes have also achieved significant success, offering effective solutions for the treatment of refractory organic contaminants. This article systematically elucidated the effectiveness, progress, and shortcomings of membrane-based technologies in the field of ECs treatment in recent years. The trends of membrane-based technologies in the field of removal of ECs in the past two decades were described in detail, with a bibliometric analysis. The management situation of newly discovered microplastics (MPs) and antibiotic resistance genes (ARGs) was also discussed. This review provided reasonable insights into the application of membrane-based technologies in the removal of ECs and offers suggestions for future research directions.

Preparation of an adsorptive membrane of polyvinylidene fluoride incorporated functionalized boron nitride nanosheets for arsenic removal

Incorporating nanomaterials into membranes will enhance wastewater treatment efficiency with their unique characteristics, such as higher permeability, thermal stability, surface roughness, hydrophilicity, and fouling control. In this study, the surface modified boron nitride with phosphoric acid 2-hydroxyethyl methacrylate ester (PA/BN) was grafted with polyethylene glycol (PEG) via conventional grafting. The PEG grafted PA/BN (PEG-g-PA/BN) melt blended with polyvinylidene fluoride (PVDF) resin by using an internal mixer at different mass percentages (100% PVDF (PVDF), 3% PEG-g-PA/BN + 97% PVDF (97:3 BN), 5% PEG-g-PA/BN + 95% PVDF (95:5 BN), 7% PEG-g-PA/BN + 93% PVDF (93:7 BN), and 7% PEG-g-PA/BNNS + 93% PVDF (93:7 BNNS). Phase inversion technique was used to cast the blended mixture into a thin membrane. The prepared membranes were analyzed with different characterization techniques to determine chemical composition, crystallinity, morphology, and thermal properties. The prepared composite membrane was evaluated in terms of water permeability, anti-fouling resistance, and solute rejection efficiency with deionized water, bovine serum albumin, and arsenic solution as well. PVDF membranes show high water flux and porosity. The water flux and porosity of the blends decrease as the percentage of PEG-g-PA/BN increases. However, the highest removal capacity for arsenic was observed at 93:7 BN. The adsorption of arsenic ions takes place via complexation with PA/BN in the PVDF matrix. This was confirmed with field emission scanning electron microscopy–energy-dispersive X-ray analysis and X-ray photoelectron spectroscopy analyses.