Polysulfone Research Articles

Membranes fouling propensity of PSF/GO hollow fiber mixed matrix membranes for water treatment ultrafiltration application

The study investigated the fouling propensity of polysulfone (PSF) hollow fiber (HF) mixed matrix membranes modified with 1.0 wt.% graphene oxide (GO). Using scanning electron microscopy (SEM), atomic force microscopy (AFM), water contact angle (WCA), and mechanical assessments, the structural characteristics of both untreated and GO‐modified PSF HF membranes were examined. Filtration experiments included pure water and model contaminants such as bovine serum albumin (BSA), humic acid (HA), E. coli, and oil‐in‐water emulsion. The GO‐modified membranes demonstrated a significant enhancement in antifouling performance, recovering over 90% of their initial pure water flux with HA and oil, indicating high resistance to irreversible fouling. Additionally, the GO‐modified membranes showed superior oil separation efficiency. However, fouling parameters for BSA were similar for both membrane types, suggesting that GO does not significantly affect membrane‐BSA interactions. Both types of membranes displayed high retention capabilities for E. coli, with no noticeable improvement due to GO addition. This study highlights the potential of GO‐modified PSF HF membranes in enhancing antifouling performance and oil separation efficiency.

Inter‐tow toughness modification of carbon fiber reinforced cyanate resin matrix composites

AbstractCarbon fiber‐reinforced cyanate ester resin matrix composites (CF/CE) are widely used in aerospace for their high‐temperature resistance and wave‐absorbing properties. However, CF/CE is prone to interlaminar delamination during the curing molding process or practical applications due to the brittleness of CE resin. In this study, we use polyether sulfone (PES) as a toughening layer through the inter‐tow toughening method to prepare PES inter‐tow toughened CF/CE (CF/CE‐P) and to investigate their thermal, mechanical, and microscopic morphology. We find that CF/CE‐P has a higher glass transition temperature (Tg) and a lower coefficient of thermal expansion (CTE) than those of CF/CE composites. The flexural strength, flexural modulus, interlaminar shear strength (ILSS), and impact toughness of CF/CE‐P with 15 wt% PES is increased by 34%, 15%, 34%, and 45%, respectively, compared to CF/CE. In addition, the mode I interlaminar fracture toughness (GIC) of CF/CE‐P with 15 wt% PES is 1.86 times that of CF/CE.Highlights The inter‐tow toughening technique on a three‐dimensional scale is proposed. Model I interlaminar fracture toughness increased by 86% after inter‐tow toughness modification carbon fiber‐reinforced cyanate ester resin matrix composites. The composite material exhibits improved toughness and thermal performance. The prepreg preparation process is suitable for continuous industrial production.

Separation properties and fouling resistance of polyethersulfone membrane modified by fungal chitosan

AbstractThis research explores the enhancement of polyethersulfone (PES) membranes through the incorporation of chitosan derived from the lignicolous fungus Ganoderma sp. Utilizing wet phase inversion and solution casting techniques, chitosan was successfully integrated into the PES matrix, as confirmed by Fourier Transform Infrared Spectroscopy (FT-IR), which indicated a high deacetylation degree of 75.7%. The incorporation of chitosan significantly increased the membrane hydrophilicity, as evidenced by a reduction in the water contact angle and a substantial improvement in pure water permeability, from 17.9 L m-2 h-1 bar-1 to 27.3 L m-2 h-1 bar-1. The membrane anti-fouling properties were also notably enhanced, with the Flux Recovery Ratio (FRR) increasing from approximately 60–80%. Moreover, the chitosan-modified PES/CS membrane, particularly at a 5% chitosan concentration, demonstrated exceptional efficacy in pollutant removal, achieving over 90% elimination of total suspended solids, cadmium (Cd), and lead (Pb), alongside a 79% reduction in color during the treatment of textile wastewater.

Polyethersulfone mixed matrix membranes modified with pore formers and Ag-titanate nanotubes: physicochemical characteristics and (bio)fouling study.

In the presented studies it was hypothesized that the modification of a polymeric membrane with a pore former and a hybrid nanomaterial composed of titanate nanotubes with deposited Ag nanoparticles (Ag-TNTs NPs) can protect the membrane from the microbial growth, and thus enhance its resistance to biofouling. Polyethersulfone (PES) membranes were prepared by the wet phase inversion, and polyvinylpyrrolidone (PVP) and poly(ethylene glycol) (PEG) were used as pore formers. The membranes were characterized in terms of morphology, topography, permeability, separation characteristics, and anti-(bio)fouling properties as well as antibacterial activity. The membranes modified with porogens and Ag-TNTs revealed improved hydrophilicity and water permeability compared to the unmodified membrane, from 58 to 66%. Moreover, the improvement in rejection of model dextrans and PEG upon application of the NPs was found. However, the use of PVP or PEG had a negative influence on the resistance to fouling by bovine serum albumin, i.e., ca. 35% of decline of permeate flux was noticed after 2h of ultrafiltration of BSA. On the contrary, both porogens and NPs contributed to biofouling mitigation. The introduction of pore formers had a positive effect on the inhibition of Escherichia coli growth by the membrane containing Ag-TNTs. The log reduction of bacteria varied from 3.17 to 3.3 in case of stirred and filtration system.

Bimetallic PdPt Nanoparticles Decorated PES Membranes for Enhanced H2 Separation.

Hydrogen separation has significant importance in diverse applications ranging from clean energy production to gas purification. Membrane technology stands out as a low-cost and efficient method to address the purpose. The development of efficient gas-sensitive materials can further bolster the membrane's performance. In this pursuit, bimetallic PdPt nanoparticles were synthesized using a wet chemical approach and were strategically decorated onto poly(ether sulfone) (PES) membranes. The fibrous morphology of the PES membranes provided an ideal platform for the decoration of nanoparticles, promising enhanced gas transport properties. Prior to the attachment of nanoparticles, the membranes were pretreated under UV light to enhance their surface properties and facilitate improved adhesion. The synthesized bimetallic nanoparticles were characterized by using transmission electron microscopy and X-ray photoelectron spectroscopy for their morphological and elemental analysis. Furthermore, the engineered membranes were characterized using various techniques, such as Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, and field emission scanning electron microscopy (FESEM) with rigorous scrutiny to ensure a comprehensive understanding of their structural, chemical, and morphological properties. The membranes were examined for their separation performance using pure H2, N2, and CO2 gases, and the results revealed a 30% increment in H2 permeability and 40 and 42% increments in H2/CO2 and H2/N2 selectivity, respectively. These findings confirmed the critical role of tailored material design and synthesis strategies in advancing membrane technologies for H2 separation applications.

Enhancing CO2/N2 and CO2/CH4 Separation Properties of PES/SAPO-34 Membranes Using Choline Chloride-Based Deep Eutectic Solvents as Additives

CO2 separation is an important environmental method mainly used in reducing CO2 emissions to mitigate anthropogenic climate change. The use of mixed-matrix membranes (MMMs) arrives as a possible answer, combining the high selectivity of inorganic membranes with high permeability of organic membranes. However, the combination of these materials is challenging due to their opposing nature, leading to poor interactions between polymeric matrix and inorganic fillers. Many additives have been tested to reduce interfacial voids, some of which showed potential in dealing with compatibility problems, but most of them lack further studies and optimization. Deep eutectic solvents (DESs) have emerged as IL substitutes since they are cheaper and environmentally friendly. Choline chloride-based deep eutectic solvents were studied as additives in polyethersulfone (PES)/SAPO-34 membranes to improve CO2 permeability and CO2/N2 and CO2/CH4 selectivity. SAPO-34 crystals of 150 nm with a high surface area and microporosity were synthesized using dry-gel methodology. The PES/SAPO-34 membranes were optimized following previous work and used in a defined composition, using 5 or 10 w/w% of DES during membrane preparation. All MMMs were characterized by their ideal gas permeability using N2 and CO2 pure gasses. Selected membranes were also tested using CH4 pure gas. The results presented that 5 w/w%, in polymer mass, of ChCl–glycerol presented the best result over the synthesized membranes. An increase of 200% in CO2 permeability maintains the CO2/N2 selectivity for the non-modified PES/SAPO-34 membrane. A CO2/CH4 selectivity of 89.7 was obtained in PES/SAPO-34/ChCl-glycerol membranes containing 5 w/w% of this DES, which is an outstanding ideal separation performance for MMMs when compared to other results in the literature. FTIR analysis reiterates the presence of glycerol in the membranes prepared. Dynamic Mechanical Thermal Analysis (DMTA) shows that the addition of 5 w/w% of DES does not impact the membrane flexibility or polymer structure. However, in concentrations higher than 10 w/w%, the inclusion of DES could lead to high membrane rigidification without impacting the overall thermal resistance. SEM analysis of DES-enhanced membranes presented asymmetric final membranes and reaffirmed the results obtained in DMTA about rigidified structures and lower zeolite–polymer interaction with higher concentrations of DES.

Developing a novel polysulfone/chitosan membrane incorporated with green synthesized CuO from aloe vera extract for toxic dye removal

AbstractThe environment and public health have been protected by the simple, non‐destructive, and ecologically benign process used for fabricating membranes. In this study, a low‐cost wastewater treatment membrane is made from raw materials followed by phase inversion approach. A typical organic pollutant that has earned a poor track record for gradually harming aquatic life. Thus, the membrane technology is used to minimize the water contaminated by dyes. To treat wastewater, a membrane was developed by combining green synthesized CuO nanoparticles with polysulfone (PS) and chitosan (CS). The developed membranes were analyzed using x‐ray photoelectron spectroscopy, contact angle, Fourier transform infrared, scanning electron microscopy, transmission electron microscope, and x‐ray diffraction techniques. The developed membrane, along with the nanoparticles and additives, confirmed its crystalline confirmation, hydrophilicity, arrangement of structures, and morphological modifications. CuO nanoparticles were prepared using aloe vera extract, and incorporated into a mixed matrix membrane was utilized for the congo red (CR) and methylene blue (MB) adsorption processes. The absorption capacity was analyzed via UV spectroscopy makes it potentially important for membrane performance. Therefore, the resulting membrane could be used as a substrate for dye removal applications.

Bi-Functional Agarose-Filled Porous Polysulfone Protective Layer for Dendrite-Free Zn Anode.

The uneven electric field and slow Zn2+ desolvation lead to rapid dendrite growth during Zn plating and stripping, which severely deteriorates the performance of Zn metal anodes (ZMAs) in Zn-ion batteries (ZIBs). Although polymer-based artificial protective (PBAP) layers are widely applied to homogenize the electric field of ZMAs, they often fail to promote the desolvation process that eventually induces Zn dendrite growth. Herein, a bi-functional protective layer, comprising a finger-like porous matrix of polysulfone (PSF) and a hydroxyl-rich filler of agarose (AG), is constructed to suppress Zn dendrite growth. COMSOL simulation demonstrates the ZMAs with bi-functional protective layers (Zn@PSF/AG) exhibit uniform electric field and Zn2+ distribution. Besides, the Zn@PSF/AG has both low desolvation energy and nucleation overpotential, effectively promoting the desolvation of Zn2+. Therefore, the Zn@PSF/AG symmetric cell exhibits excellent cycling performance, achieving 4200h at 1mA cm-2/1 mAh cm-2 and 1000h at 5mA cm-2/5 mAh cm-2. When coupling with ZnxV2O5 (ZnVO) cathode, the ZnVO‖Zn@PSF/AG full cell shows similarly high cycling stability, maintaining 72% of its capacity after 7000 cycles at 10 A g-1. This research highlights the positive roles of PBAP layer with multi-functional matrix-filler structure in developing long-life ZIBs.

Hydrocarbon-based composite membranes containing sulfonated Poly(arylene thioether sulfone)-grafted 2D crown ether framework coordinated with cerium ions for PEMFC applications

We propose a novel strategy to develop sulfonated poly(arylene ether sulfone) (SPAES) composite membranes that can simultaneously improve the physicochemical stability and proton conductivity of hydrocarbon-based membranes for PEMFC applications. This strategy involves the use of a sulfonated poly(arylene thioether sulfone)-grafted 2D crown ether framework coordinated with cerium3+ ions (SATS–C2O–Ce) as a promising filler material. SATS-C2O, a highly sulfonated polymer-grafted 2D framework containing crown ether holes in its skeletal structure, was prepared via self-condensation using halogenated phloroglucinol as a multifunctional building unit to form C2O, followed by condensation using SATS to graft the sulfonated polymer onto its edge. Ce3+ ions were directly coordinated within the crown ether holes of SATS-C2O via a simple doping process using aqueous Ce solution. The SPAES composite membranes containing SATS–C2O–Ce (SPAES/SATS–C2O–Ce) exhibited exceptional dimensional stability and mechanical toughness. The remarkable chemical stability of SPAES/SATS–C2O–Ce compared to that of pristine SPAES and SPAES/Ce (containing the same amount of Ce3+ ions but without SATS-C2O) was attributed to the well-dispersed state of Ce3+ ions within the SPAES matrix. Furthermore, the enhanced proton conductivity of SPAES/SATS–C2O–Ce surpassed those of pristine SPAES, SPAES/C2O, and SPAES/Ce by the formation of additional proton-conducting channels provided by the sulfonic acid groups of SATS–C2O–Ce, along with the improved water uptake capability of SPAES.

Comprehensive properties analysis of epoxy composites synergistically toughened with liquid nitrile rubber and polyethersulfone

In this paper , epoxy resin (EP) composites with different phase structures were prepared by introducing hydroxyl-terminated liquid nitrile rubber (HTBN) and hydroxyl-terminated polyethersulfone (PES) individually or simultaneously into the resin matrix. The results revealed that the rational distribution of phase structure of rigid PES and flexible HTBN can effectively contributed to the enhancement in their mechanical and electrical insulation strengths. The synergistic effect of the two reinforcing fillers granted the optimized ternary composite a tougher structural network, leading to significant improvements of 73.13% and 18.98% in mechanical impact strength and electrical breakdown strength, respectively, compared to the pristine EP. Furthermore, compared to HTBN, PES exhibited inhibited HTBN dielectric interfacial polarization and EP molecular chain segment relaxation, resulting in decreased dielectric constant and loss in the composites. This study provide insights into the dielectric properties and design strategies for the development of resin-based dielectric materials, ensuring their broader applicability.

Development of a Negatively Charged Polyether Sulfone Membrane Enriched with MIL-101(Cr)-Modified Magnetic Activated Pyrolytic Coke for Enhanced Dye Removal, Permeability, and Antifouling Properties

Developing high-performance nanofiltration membranes for effectively treating wastewater contaminated with organic pollutants has become increasingly important. Given the hazardous nature of these contaminants, proper treatment of wastewater is crucial before it is released into natural water bodies. This study synthesized a novel composite membrane by incorporating Fe3O4@APC@MIL-101(Cr) nanocomposites into a polyether sulfone (PES) matrix using a phase inversion technique. The inclusion of 0.5wt.% Fe3O4@APC@MIL-101(Cr) significantly enhanced the membrane's hydrophilicity, porosity, and surface characteristics. The optimized membrane achieved an impressive pure water flux (PWF) of 90.24L/m²h, reflecting a 400% improvement over pristine PES membranes. Moreover, it exhibited excellent rejection rates of 97.21% for crystal violet (CV) and 99.43% for methylene blue (MB), alongside a rejection efficiency of 57.73% for the anionic dye methyl orange (MO). The antifouling performance was notably improved, as evidenced by an increase in the flux recovery ratio (FRR) from 46% for bare PES membranes to 81.11% for hybrid membranes. Additionally, the effects of various salt types on the membrane's separation performance were investigated. The Fe3O4@APC@MIL-101(Cr) modified PES membranes demonstrate significant potential as effective candidates for treating wastewater contaminated with dye pollutants.

Electrospun Sulfonated Poly(ether ether ketone) and Chitosan/Poly(vinyl alcohol) Bifunctional Nanofibers to Accelerate Proton Conduction at Subzero Temperature.

Multilayered microstructures can accelerate the proton conduction process in proton exchange membranes (PEMs). Herein, we design and construct PEMs with microstructures based on bifunctional nanofibers and sulfonated poly(ether ether ketone) (SPEEK) nanofibers. Specifically, the bifunctional nanofibers composed of poly(vinyl alcohol) and chitosan are prepared and then combined with the electrospun SPEEK nanofibers. The stable microstructure is derived from the compatible interfacial property of nanofibers and the formed hydrogen bonds. The multilayered microstructure consisting of nanofibers accelerates the proton conduction even at subzero temperature because of regulating the proton conduction pathways. Specifically, the (SKNF/CPNF/SKNF)/PA membrane exhibits the proton conductivities of (0.951 ± 0.138) × 10-2 S/cm at -30 °C and (7.32 ± 0.37) × 10-2 S/cm at 160 °C. Additionally, the fine proton conductivity stability is demonstrated by the proton conductivity in the long-term test and the cooling/heating cycle test, such as 1.67 × 10-2 S/cm at -30 °C (after 1000 h), 4.52 × 10-2 S/cm at 30 °C (after 810 h), 1.12 × 10-2 S/cm at -30 °C, and 1.01 × 10-1 S/cm at 30 °C in the cooling/heating process (5 cycles). The single fuel cell possesses an open-circuit voltage of 0.886 V and a peak power density of 0.508 W/cm2 at 130 °C.

Light-responsive zwitterionic membrane surface modification for antifouling and antibacterial application

Light-responsive surface modifications offer a promising solution for reducing membrane fouling by enabling remote, contactless cleaning without altering the chemical environment. While traditional methods make membranes hydrophilic to resist fouling, biofouling remains difficult to remove and often requires harsh bactericidal treatments. With the rise of antimicrobial resistance (AMR), there is a pressing need for alternative, non-bactericidal strategies to control biofilm growth. In this study, we developed an efficient approach by coating commercial ultrafiltration polyethersulfone (PES) membranes with a copolymer of light-responsive azobenzene (AZO) and zwitterionic sulphobetaine methacrylate (SBMA). The photochemical conversion efficiency and photokinetic parameters of the copolymer, due to light-induced trans–cis-trans conversion, were systematically determined. During filtration, the modified membranes showed excellent resistance to reversible fouling with bovine serum albumin (BSA). The fouled membrane became reusable after near-complete removal of irreversible fouling, including bacteria (Pseudomonas aeruginosa), by activating the AZO units with UV–vis light, providing an effective strategy for fouling control.

Ultra-fast interlayer construction strategy for the preparation of NF membranes with high Li+/Mg2+ separation performance

Nanofiltration (NF) membranes have demonstrated significant potential in lithium extraction from salt-lake brines due to their superior selectivity in separating monovalent cations from divalent cations. In this paper, NF membranes with high permeate flux and high lithium-magnesium separation factor (SLi,Mg) were prepared by using a polyamide (PA) layer as the separation layer, RA-PEI as the interlayer, and a polysulfone (PSf) membrane as the substrate membrane. Notably, the RA-PEI co-deposition modification method is an ultra-fast substrate modification method, requiring only 1s for modifying PSf substrates. At the same time, RA-PEI firmly adheres to the surface of the PSf substrate by the synergistic effects of intermolecular hydrogen bonding interactions and π-π interactions. This was further verified by comparing the adsorption energies of different kinds of organic interlayers and PSf substrates obtained from molecular dynamics (MD) simulations. Correlation characterization showed that the RA-PEI interlayer endowed the NF membranes with reduced average pore size as well as attenuated electronegativity, thus realizing the efficient separation of Mg2+ and Li+. The performance assessment showed that the membrane containing RA-PEI interlayer exhibited excellent separation performance and permeate flux in simulated salt-lake brine (2000 ppm, WMg/Li = 20), where SLi,Mg (92.8) and permeate flux (16.7 L·m−2·h−1·bar−1) were improved by 7.8 and 2.2 times, respectively, in comparison to the pristine NF membrane. Therefore, this work provides a useful contribution to the practical use of NF membranes for lithium extraction from salt lakes.

Calcium Silicate Promoting the Upcycling Potential of Polysulfone Medical Waste in Load-Bearing Applications

Polysulfone (PSF) medical waste can be effectively repurposed due to its excellent mechanical properties. Due to the increasing need for load-bearing bone implants, it is crucial to prioritize the development of biocompatible polymer–matrix composites. Calcium silicate (CaSi), known for its osteogenesis and antibacterial properties, is widely used in medical applications. In this study, recycled PSF plastics in fiber or nanoparticle forms and commercial PSF products were used to create PSF-based composites filled with three different amounts (10, 20, and 30 vol%) of CaSi. The green compact was heat-treated at various temperatures. Experimental results showed that the mechanical interlocking of the PSF matrix and CaSi filler occurred due to the liquefaction of PSF fibers or nanoparticles during heat treatment. When the composite contained 20% CaSi, the obtained three-point bending strength exceeded 60 MPa, falling within the reported strength of compact bone. There was a concurrent improvement in the biocompatibility and antibacterial activity of the PSF-based composites with the increasing amount of CaSi. Considering their mechanical properties and antibacterial activity, the 20% CaSi-containing PSF-based composites treated at 240 °C emerged as a promising candidate for bone implant applications. This study demonstrated the feasibility of upcycling medical waste such as PSF as a matrix, opening doors for its potential usage in the medical field.

Mitigating Membrane Fouling in Abattoir Wastewater Treatment: Integration of Pretreatment Step with Zwitterion Modified Graphene Oxide–Polyethersulfone Composite Membranes

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.

Synthesis of furan-2-ones and spiro[furan-2,3ʹ-indoline] derivatives using polyether sulfone sulfamic acid catalysis

Polyether sulfone sulfamic acid (PES-NHSO3H) was prepared by simple sulfonation of a modified polyether sulfone. The number of acidic sites (SO3H) was determined to be 4.23 mmol H+/g by acid-base titration and 4.29 mmol H+/g by barium sulfate test. PES-NHSO3H was used as an efficient acidic catalytic system for the preparation of functionalized furan-2-ones and 2ʹ,5-dioxo-5 H-spiro[furan-2,3 ʹ -indoline]-3-carboxylate derivatives via the three-component reaction of anilines, aldehydes/1-ethylindoline-2,3-dione, and diethyl acetylene dicarboxylate in high yields (85–97%). The effect of polar and non-polar solvents on the productivity of the reaction was investigated. The catalyst was recovered 11 times without losses in catalytic potential.

Computational Analysis of Amine Functionalization in Zwitterionized Polyether Sulfone Dialysis Membranes

Hemodialysis is a critical treatment for patients with end-stage renal disease (ESRD) who lack kidney transplant options. The compatibility of hemodialysis membranes is vital, as incompatibility can trigger inflammation, coagulation, and immune responses, potentially increasing morbidity and mortality among patients with ESRD. This study employed molecular dynamics simulation (MDS) and molecular docking to assess the hemocompatible properties of Polyether Sulfone (PES) membranes modified via two distinct amine functionalization techniques. The molecular docking results demonstrated that side amine functionalization exhibited a lower affinity energy (−7.6) for fibrinogen compared to the middle amine functionalization (−8.2), suggesting enhanced antifouling properties and superior hemocompatibility. Additionally, side amine functionalization formed hydrogen bonds with four amino acids, enhancing its resistance to protein adhesion compared to three amino acids in the middle amine structure. Furthermore, the molecular dynamics simulations revealed differences in water mobility, with the side amine functionalized membranes showing a lower mobility value (9.74 × 10−7) than those treated with the middle amine method (9.85 × 10−7), indicating higher water stability and potentially better patient outcomes. This study’s findings contribute to the design of more efficient and safer hemodialysis treatments by optimizing membrane materials.

Laser-induced nucleation of urea through the control of Insoluble Impurity

The mechanism of non-photochemical laser-induced nucleation (NPLIN) was investigated through the crystallization of urea crystals in supersaturated (151%) aqueous solutions. To detect the role of impurities in NPLIN, the effect of filtration, doping and laser irradiation position on nucleation probability were studied, respectively. As particles larger than the filter pore size in the solution were almost removed by syringe filter with poly (ether sulfone) membrane, the NPLIN probability was evidently suppressed by filtration when the pore sizes of filter were used from 1 μm to 0.45 μm. The inhibition of NPLIN after filtration could be reversed to varying degrees by adding several kinds and concentrations of impurities into the filtered solution; as the solid particles were extra added, age after cooling for samples was no longer necessary. The increase in the NPLIN probability with the irradiation height decreases was observed when samples were irradiated at different vertical positions within the sample vial. The experimental results were analyzed with reference to the known mechanisms. As nucleation probability through NPLIN can be controlled by pore size of syringe filter, doping or laser irradiation position, several functions were established to analyze the nucleation probability distribution under the effect of these three factors. These experimental results were discussed with reference to the known mechanisms proposed for NPLIN.

Visible-light-activated Fe2O3–TiO2 nanoparticles enhance biofouling resistance of polyethersulfone ultrafiltration membranes against marine algae Chlorella vulgaris

This study investigated the modification of polyethersulfone (PES) ultrafiltration membranes with TiO2 and Fe2O3–TiO2 nanoparticles to enhance their hydrophilicity and biofouling resistance against the marine microalgae Chlorella vulgaris. It is a common freshwater and marine microalga that readily forms biofilms on membrane surfaces, leading to significant flux decline and increased operational costs in ultrafiltration processes. The microalgae cells and their extracellular polymeric substances (EPS) adhere to the membrane surface, creating a dense fouling layer that impedes water permeation. The modified membranes were characterized using contact angle measurements, scanning electron microscopy, and pure water flux/resistance tests. Short-term ultrafiltration experiments evaluated the membranes’ antifouling performance by measuring flux decline, flux recovery ratio, and relative flux reduction during C. vulgaris filtration. The TiO2 membrane showed improved hydrophilicity and antifouling over the pristine PES membrane, while the Fe2O3–TiO2 nanocomposite membrane exhibited the best performance. It reduced the water contact angle and showed only a 5% relative flux reduction compared to 60% for the pristine membrane. SEM images confirmed reduced microalgal deposition on the nanocomposite surface. Long-term tests with microalgal cells under dark and visible light conditions in saline water further assessed the membranes’ biofouling resistance. The Fe2O3–TiO2 membrane maintained 59 L/m2 h water flux under visible light after immersion in the microalgal solution, outperforming the pristine (38 L/m2 h) and TiO2 (52 L/m2 h) membranes. This superior antifouling was attributed to photocatalytic generation of reactive oxygen species inhibiting microalgal adhesion. This study demonstrates a promising strategy for mitigating biofouling in membrane-based water treatment and desalination processes.