Search Results (43)

Sulfonated poly(ether ether ketone) (SPEEK) is one of the most studied ionic polymers for polymer electrolyte membranes (PEMs) in fuel cells (PEMFCs). To improve its proton conductivity, novel SPEEK/praseodymium-doped zinc spinel ferrite composite membranes of 130–170 μm thickness were prepared via ultrasound-assisted dispersion of various proportions of synthesized doped ferrite nanoparticles into the polymer solution, followed by a simple solution-casting method. The morphology (as observed by SEM and confirmed by DMA) and the conducted physical and chemical tests typical for PEMs, such as water uptake (32–44% at 80 °C), ionic exchange capacity (1.67–1.80 mEq/g), chemical (around 1% loss in Fenton reagent after 24 h), thermal stability (up to 190 °C) and tensile strength (39–50 MPa), were proven to depend on the content of inorganic filler in the composite (up to 5%). The proton conductivity of composite membranes (0.21–2.82 × 10⁻² S/cm at 80 °C) was assessed by broadband dielectric spectroscopy. The membrane with a content of 0.25 wt.% ZnFe_1.96Pr_0.04O₄ showed the best proton conductivity (3.41 × 10⁻² S/cm at 60 °C), as compared to 1.60 × 10⁻² S/cm for Nafion117 measured under the same conditions, demonstrating its suitability as a PEM for fuel cell applications. Full article

Spin-spray-assisted layer-by-layer (LbL) assembly is an innovative method for producing nanostructured thin films due to its rapid assembly and extensive coverage of substrates. In this study, a nanofiltration (NF) membrane consisting of multilayers of polyethyleneimine (PEI) and poly(sodium-4-styrene sulfonate) (PSS) was fabricated on a polysulfone (PSF) support. The resulting membrane was further coated with a metal–organic framework (MOF303). The resulting (PEI/PSS)₅-MOF303 showed a rejection rate of 18.94 ± 1.58% and a permeability of 0.91 ± 0.13 L/(h·bar·m²)while also showing enhanced antifouling properties. This work explores the possibility of spin-spray-assisted LbL assembly as a promising method for fabricating membranes. Full article

Polyzwitterion (PZW) hydrogel has excellent marine anti-biofouling performance, but it is difficult to effectively work for a long time in natural seawater due to its weak mechanical strength. In this study, a new natural rubber (NR)-PZW composite hydrogel has been reported for long-term anti-biofouling by simply dispersing NR latex into the poly(sulfobetaine methacrylate) (PSBMA) hydrogel network. First of all, owing to the PZW hydrogel network having an anti-polyelectrolyte effect, this NR-PZW hydrogel can provide outstanding anti-biofouling performance, including broad-spectrum anti-bacteria, anti-algae, and anti-protein properties in marine environments. Furthermore, it has a composited natural rubber nanoparticle with a hydrophilic negatively charged outer protein membrane, which can uniformly disperse in the hydrogel to significantly improve its mechanical properties. Therefore, this composited hydrogel can provide not only highly enhanced tensile strength (0.52 MPa) but also ultra-high breaking elongation (738%), which can effectually resist harsh seawater environments. As a result, the NR-PZW composite hydrogel can achieve excellent anti-biofouling performance for more than 3 months within a real marine environment. This work can provide an excellent, robust polyzwitterionic hydrogel for long-term marine anti-biofouling, which will also inspire new strategies for anti-biofouling materials. Full article

Composite polyethersulfone (PES) membranes containing N-aminoethyl piperazine propane sulfonate (AEPPS)-modified graphene oxide (GO) were integrated with either of the two pretreatment processes (activated carbon (AC) adsorption or polyelectrolyte coagulation) to assess their effectiveness in mitigating membrane fouling during the treatment of abattoir wastewater. The AEPPS@GO-modified membranes, as compared to the pristine PES membranes, showed improved hydrophilicity, with water uptake increasing from 72 to 118%, surface porosity increasing from 2.34 to 27%, and pure water flux (PWF) increasing from 235 to 673 L.m⁻²h⁻¹. The modified membranes presented improved antifouling properties, with the flux recovery ratio (FRR) increasing from 59.5 to 93.3%. This study compared the effectiveness of the two pretreatment processes, AC, coagulation, and the integrated system (coagulation/AC-UF membrane), in the removal of natural organic matter (NOM) and improvement of abattoir wastewater’s pH, electrical conductivity, TDS, and turbidity. The integrated systems produced improved water quality in terms of pH, EC, TDS, turbidity, and organic content. The fluorescence excitation–emission matrix (FEEM) analysis exhibited almost no fluorescence peak post-treatment following organic loading removal. The quality of the water met the South African non-potable water reuse standards. The sole membrane treatment systems exhibited good fouling resistance without the pretreatment systems; however, integrating these systems can offer extended longer filtration periods, thereby assisting in cost aspects of the abattoir wastewater treatment system. Full article

The present article introduces a strategy for controlling oxidation and reduction reactions within polymer electrolyte membrane (PEM) networks as a means of enhancing storage capacity through the complexation of dissociated lithium cations with multifunctional groups of the polymer network. Specifically, co-polymer networks based on polysulfide (PS) and polyoxide (PO) precursors, photo-cured in the presence of succinonitrile (SCN) and lithium bis(trifluoro methane sulfonyl imide) (LiTFSI) salt, exhibited ionic conductivity on the order of mid 10⁻⁴ S/cm at ambient temperature in the 30/35/35 (weight %) composition. Lithium titanate (LTO, Li₄Ti₅O₁₂) electrode was chosen as an anode (i.e., a potential source of Li ions) against lithium iron phosphate (LFP, LiFePO₄) cathode in conjunction with polysulfide-co-polyoxide dual polyelectrolyte networks to control viscosity for 3D printability on conformal surfaces of drone and aeronautic vehicles. It was found that the PS-co-PO dual network-based polymer electrolyte containing SCN plasticizer and LiTFSI salt exhibited extra storage capacity (i.e., specific capacity of 44 mAh/g) with the overall specific capacity of 170 mAh/g (i.e., for the combined LTO electrode and PEM) initially that stabilized at 153 mAh/g after 50th cycles with a reasonable capacity retention of over 90% and Coulombic efficiency of over 99%. Of particular interest is the observation of the improved electrochemical performance of the polysulfide-co-polyoxide electrolyte dual-network relative to that of the polyoxide electrolyte single-network. Full article

Pervaporation is considered the most promising technology for dehydration of bioalcohols, attracting increasing attention as a renewable energy source. In this regard, the development of stable and effective membranes is required. In this study, highly efficient membranes for the enhanced pervaporation dehydration of ethanol were developed by modification of sodium alginate (SA) with a polyethylenimine (PEI) forming polyelectrolyte complex (PEC) and graphene oxide (GO). The effect of modifications with GO or/and PEI on the structure, physicochemical, and transport characteristics of dense membranes was studied. The formation of a PEC by ionic cross-linking and its interaction with GO led to changes in membrane structure, confirmed by spectroscopic and microscopic methods. The physicochemical properties of membranes were investigated by a thermogravimetric analysis, a differential scanning calorimetry, and measurements of contact angles. The theoretical consideration using computational methods showed favorable hydrogen bonding interactions between GO, PEI, and water, which caused improved membrane performance. To increase permeability, supported membranes without treatment and cross-linked were developed by the deposition of a thin dense layer from the optimal PEC/GO (2.5%) composite onto a developed porous substrate from polyacrylonitrile. The cross-linked supported membrane demonstrated more than two times increased permeation flux, higher selectivity (above 99.7 wt.% water in the permeate) and stability for separating diluted mixtures compared to the dense pristine SA membrane. Full article

Two-dimensional (2D) nanomaterial-based membranes feature attractive properties for molecular separation and transport, which exhibit huge potential in various chemical processes. However, the low permeability and bio-fouling of the MXene membrane in water treatment become huge obstacles to its practical application. Herein, a highly permselective and anti-bacterial 2D nanofiltration membrane is fabricated by intercalating a polycation of polydiallyldimethylammonium chloride (PDDA) into the Ti₃C₂T_x MXene laminar architecture through a facile and patternable electrostatic assembly strategy. As a result, the as-fabricated Ti₃C₂T_x/PDDA composite membrane exhibits higher water permeance up to 73.4 L m⁻² h⁻¹ with a rejection above 94.6% for MgCl₂. The resultant membrane simultaneously possesses good resistance to swelling and long-term stability in water environments, even after 8 h. Additionally, the Ti₃C₂T_x/PDDA membrane also demonstrates a high flux recovery ratio of nearly 96.1% to bovine serum albumin proteins after being cleaned. More importantly, the current membrane shows excellent anti-adhesive and anti-microbial activity against Gram-negative Escherichia coli (E. coli) and Gram-positive Staphylococcus aureus (S. aureus), with inhibition rates of 90% and 95% against E. coli and S. aureus, respectively. This holds great potential for the application of the polyelectrolyte-intercalated MXene membrane in serving as a promising platform to separate molecules and/or ions in an aquatic environment. Full article

In this study, novel proton exchange membranes (PEMs) based on a composite of sulfonated polyacrylonitrile (SPAN), sulfonated polyglycidyl methacrylate (SPGMA), or sulfonated poly(acrylonitrile-co-glycidyl methacrylate) (SP(AN-co-GMA))/polyvinyl chloride (PVC) were developed to be used for direct methanol fuel cells (DMFCs). After polymerization and sulfonation of the prepared polymers, the polyelectrolyte membranes were prepared by the casting and solvent evaporation technique for sulfonated homo- or co-polymers with polyvinyl chloride (PVC) composites. The resulting membranes were characterized by Fourier infrared and Raman spectral analyses, X-ray diffractometry, and scanning electron microscopy. The findings of this study reveal that both the thermal stability and ion exchange capacity of the composite membranes based on sulfonated copolymers were higher than that of their corresponding composites based on sulfonated homopolymers. In this context, the weight loss percentage of the prepared composite polyelectrolyte membranes did not exceed 12% of their initial weights. The IEC of all the composite membranes ranged from 0.18 to 0.48 meq/g. Thus, the IEC value increased with the increasing proportion of the glycidyl methacrylate comonomer. Moreover, the prepared PEMs based on SP(AN-co-GMA)/PVC composites showed lower methanol permeability (8.7 × 10⁻⁷ cm²/s) than that of the Nafion membranes (3.39 × 10⁻⁶ cm²/s). Therefore, these prepared PEMs are a good candidate for DMFCs applications. Full article

The increasing demand for nanofiltration processes in drinking water treatment, industrial separation and wastewater treatment processes has highlighted several shortcomings of current state-of-the-art thin film composite (TFC NF) membranes, including limitations in chemical resistance, fouling resistance and selectivity. Polyelectrolyte multilayer (PEM) membranes provide a viable, industrially applicable alternative, providing significant improvements in these limitations. Laboratory experiments using artificial feedwaters have demonstrated selectivity an order of magnitude higher than polyamide NF, significantly higher fouling resistance and excellent chemical resistance (e.g., 200,000 ppmh chlorine resistance and stability over the 0–14 pH range). This review provides a brief overview of the various parameters that can be modified during the layer-by-layer procedure to determine and fine-tune the properties of the resulting NF membrane. The different parameters that can be adjusted during the layer-by-layer process are presented, which are used to optimize the properties of the resulting nanofiltration membrane. Substantial progress in PEM membrane development is presented, particularly selectivity improvements, of which the most promising route seems to be asymmetric PEM NF membranes, offering a breakthrough in active layer thickness and organic/salt selectivity: an average of 98% micropollutant rejection coupled with a NaCl rejection below 15%. Advantages for wastewater treatment are highlighted, including high selectivity, fouling resistance, chemical stability and a wide range of cleaning methods. Additionally, disadvantages of the current PEM NF membranes are also outlined; while these may impede their use in some industrial wastewater applications, they are largely not restrictive. The effect of realistic feeds (wastewaters and challenging surface waters) on PEM NF membrane performance is also presented: pilot studies conducted for up to 12 months show stable rejection values and no significant irreversible fouling. We close our review by identifying research areas where further studies are needed to facilitate the adoption of this notable technology. Full article

In this work, fully polysaccharide based membranes were presented as self-standing, solid polyelectrolytes for application in anion exchange membrane fuel cells (AEMFCs). For this purpose, cellulose nanofibrils (CNFs) were modified successfully with an organosilane reagent, resulting in quaternized CNFs (CNF (D)), as shown by Fourier Transform Infrared Spectroscopy (FTIR), Carbon-13 (C13) nuclear magnetic resonance (¹³C NMR), Thermogravimetric Analysis (TGA)/Differential Scanning Calorimetry (DSC), and ζ-potential measurements. Both the neat (CNF) and CNF(D) particles were incorporated in situ into the chitosan (CS) membrane during the solvent casting process, resulting in composite membranes that were studied extensively for morphology, potassium hydroxide (KOH) uptake and swelling ratio, ethanol (EtOH) permeability, mechanical properties, ionic conductivity, and cell performance. The results showed higher Young’s modulus (119%), tensile strength (91%), ion exchange capacity (177%), and ionic conductivity (33%) of the CS-based membranes compared to the commercial Fumatech membrane. The addition of CNF filler improved the thermal stability of the CS membranes and reduced the overall mass loss. The CNF (D) filler provided the lowest (4.23 × 10⁻⁵ cm² s⁻¹) EtOH permeability of the respective membrane, which is in the same range as that of the commercial membrane (3.47 × 10⁻⁵ cm²s⁻¹). The most significant improvement (~78%) in power density at 80 °C was observed for the CS membrane with neat CNF compared to the commercial Fumatech membrane (62.4 mW cm⁻² vs. 35.1 mW cm⁻²). Fuel cell tests showed that all CS-based anion exchange membranes (AEMs) exhibited higher maximum power densities than the commercial AEMs at 25 °C and 60 °C with humidified or non-humidified oxygen, demonstrating their potential for low-temperature direct ethanol fuel cell (DEFC) applications. Full article

In this work, a simple method was proposed to produce dense composite polysaccharide-based membranes to be used for guided tissue and guided bone regeneration. The mucoadhesive polysaccharides chitosan (C) and xanthan gum (X) were used to produce polyelectrolyte-based complex membranes. Hydroxyapatite (HA) was added to the formulation as a potential drug carrier, in C:X:HA mass proportions equal to 1:1:0.4, 1:1:2, and 1:1:10, and also to improve membranes bioactivity and biomimetic properties. FTIR analysis indicated successful incorporation of HA in the membranes and XRD analysis showed that no changes in the HA crystalline structure were observed after incorporation. The residual mass evaluated by TGA was higher for the formulation produced at the proportion 1:1:10. The membranes produced showed asymmetrical surfaces, with distinct roughness. Increasing the HA concentration increased the surface roughness. Greater in vitro proliferation of dental pulp mesenchymal stem cells was observed on the surface of the membrane with 1:1:10 C:X:HA proportion. However, the 1:1:2 formulation showed the most adequate balance of mechanical and biological properties. These results suggest that adding HA to the membranes can influence mechanical parameters as well as cell adhesion and proliferation, supporting the potential application of these materials in regenerative techniques and the treatment of periodontal lesions. Full article

The application of electrodialysis for tartrate stabilization and reagent-free acidity correction of wine and juices is attracting increasing interest. New aliphatic membranes CJMC-3 and CJMA-3 and aromatic membranes CSE and ASE were tested to determine their suitability for use in these electrodialysis processes and to evaluate the fouling of these membranes by wine components for a short (6–8 h) operating time. Using IR spectroscopy, optical indication and measurement of surface contact angles, the chemical composition of the studied membranes, as well as some details about their fouling by wine components, was clarified. The current–voltage charsacteristics, conductivity and water-splitting capacity of the membranes before and after electrodialysis were analyzed. We found that in the case of cation-exchange membranes, complexes of anthocyanins with metal ions penetrate into the bulk (CJMC-3) or are localized on the surface (CSE), depending on the degree of crosslinking of the polymer matrix. Adsorption of wine components by the surface of anion-exchange membranes CJMA-3 and ASE causes an increase in water splitting. Despite fouling under identical conditions of electrodialysis, membrane pair CJMC-3 and CJMA-3 provided 18 ± 1 tartrate recovery with 31 · 10⁻³ energy consumption, whereas CSE and ASE provided 20 ± 1% tartrate recovery with an energy consumption of 28 · 10⁻³ Wh, in addition to reducing the conductivity of wine by 20 ± 1%. The casting of aliphatic polyelectrolyte films on the surface of aromatic membranes reduces fouling with a relatively small increase in energy consumption and approximately the same degree of tartrate recovery compared to pristine CSE and ASE. Full article

Mussels secrete protein-based byssal threads to tether to rocks, ships, and other organisms underwater. The secreted marine mussel adhesive proteins (MAPs) contain the peculiar amino acid L-3,4-dihydroxyphenylalanine (DOPA), whose catechol group content contributes greatly to their outstanding adhesive properties. Inspired by such mussel bioadhesion, we demonstrate that catechol-modified polysaccharides can be used to obtain adhesive membranes using the compaction of polyelectrolyte complexes (CoPEC) method. It is a simple and versatile approach that uses polyelectrolyte complexes as building blocks that coalesce and dry as membrane constructs simply as a result of sedimentation and mild temperature. We used two natural and biocompatible polymers: chitosan (CHI) as a polycation and hyaluronic acid (HA) as a polyanion. The CoPEC technique also allowed the entrapment of ternary bioactive glass nanoparticles to stimulate mineralization. Moreover, combinations of these polymers modified with catechol groups were made to enhance the adhesive properties of the assembled membranes. Extensive physico-chemical characterization was performed to investigate the successful production of composite CoPEC membranes in terms of surface morphology, wettability, stability, mechanical performance, in vitro bioactivity, and cellular behavior. Considering the promising properties exhibited by the obtained membranes, new adhesives suitable for the regeneration of hard tissues can be envisaged. Full article

The development of biomaterials to enable application of antimicrobial peptides represents a strategy of high and current interest. In this study, a bioparticle was produced by the complexation between an antimicrobial polypeptide and the biocompatible and biodegradable polysaccharides chitosan-N-arginine and alginate, giving rise to a colloidal polyelectrolytic complex of pH-responsive properties. The inclusion of the polypeptide in the bioparticle structure largely increases the binding sites of complexation during the bioparticles production, leading to its effective incorporation. After lyophilization, detailed evaluation of colloidal structure of redispersed bioparticles evidenced nano or microparticles with size, polydispersity and zeta potential dependent on pH and ionic strength, and the dependence was not withdrawn with the polypeptide inclusion. Significant increase of pore edge tension in giant vesicles evidenced effective interaction of the polypeptide-bioparticle with lipid model membrane. Antibacterial activity against Aeromonas dhakensis was effective at 0.1% and equal for the isolated polypeptide and the same complexed in bioparticle, which opens perspectives to the composite material as an applicable antibacterial system. Full article

Today the standard treatment for wastewater is secondary treatment. This procedure cannot remove salinity or some organic micropollutants from water. In the future, a tertiary cleaning step may be required. An attractive solution is membrane processes, especially nanofiltration (NF). However, currently available NF membranes strongly reject multivalent ions, mainly due to the dielectric effect. In this work, we present a new method for preparing NF membranes, which contain negatively and positively charged domains, obtained by the combination of two polyelectrolytes with opposite charge. The negatively charged polyelectrolyte is provided in the form of particles (polystyrene sulfonate (PSSA), d ~300 nm). As a positively charged polyelectrolyte, polyethyleneimine (PEI) is used. Both buildings blocks and glycerol diglycidyl ether as crosslinker for PEI are applied to an UF membrane support in a simple one-step coating process. The membrane charge (zeta potential) and salt rejection can be adjusted using the particle concentration in the coating solution/dispersion that determine the selective layer composition. The approach reported here leads to NF membranes with a selectivity that may be controlled by a different mechanism compared to state-of-the-art membranes. Full article