Surface Modification Of Polyethersulfone Membrane Research Articles

Vanillin as an Antifouling and Hydrophilicity Promoter Agent in Surface Modification of Polyethersulfone Membrane.

Fouling as an intricate process is considered as the main obstacle in membrane technologies, and its control is one of the main areas of attention in membrane processes. In this study, a commercial polyethersulfone ultrafiltration membrane (MWCO: 4000 g/mol) was surface modified with different concentrations of vanillin as an antifouling and hydrophilicity promoter to improve its performance. The presence of vanillin and its increasing adsorption potential trends in higher vanillin concentrations were clearly confirmed by observable changes in FTIR (Fourier transform infrared) spectra after modification. Membranes with better hydrophilicity (almost 30% lower contact angle in the best case) and higher polyethylene glycol solution (PEG) permeability were achieved after modification, where a 35–38% increase in permeability of aqueous solution of PEG was perceived when the membrane was modified at the highest exposure concentration of vanillin (2.8 g/L). After filtration of wood extract, surface modified membrane (2.8 g/L vanillin) showed better antifouling characteristics compared to unmodified membrane, as indicated by approximately 22% lower pure water flux reduction, which in turn improved the separation of lignin from the other organic compounds present in wood extract.

SURFACE MODIFICATION OF POLYETHERSULFONE MEMBRANE VIA UV-GRAFTING FOR FORWARD OSMOSIS TECHNOLOGY

In this study, UV-grafting was used in surface modification of polyethersulfone membrane (UFPES50) for forward osmosis (FO) application. Using two parameters, namely monomer concentration (acrylic acid) and grafting time, the modified membrane was characterised by attenuated total reflectance-Fourier transform infrared (ATR-FTIR), field emission scanning electron microscope (FESEM) and contact angle. The membrane was evaluated for its water permeability, solute permeability, and structural parameter. The water permeability increases as the grafting parameters increases; however, at the highest (50 g/L) monomer concentration, a sudden drop occurred due to the thickening of the grafted layer. Focusing on this monomer concentration, the grafting time was increased up to 60 minutes and it was successfully demonstrated that the modification using UV-grafting on PES membrane involved both effective grafting and chain scission. In addition, negative rejection on the modified membrane was observed

Surface modification of polyethersulfone membranes with goethite through self-assembly

Surface modification of polyethersulfone membranes with goethite through self-assembly

Heparin-like surface modification of polyethersulfone membrane and its biocompatibility

Sulfonated polyethersulfone (SPES) and poly (acrylonitrile-co-acrylic acid-co-vinyl pyrrolidone) (P(AN–AA–VP)), which provided sulfonic acid (SO3H) and carboxylic acid groups (COOH), respectively, were used to modify polyethersulfone (PES) membrane with a heparin-like surface by blending method. The SPES was prepared by sulfonation of PES using chlorosulfonic acid as the sulfonating agent, while the P(AA–AN–VP) was prepared through a free radical polymerization. The PES and modified PES membranes were prepared by a phase-inversion technique; the modified membranes showed lowered protein (bovine serum albumin, BSA; bovine serum fibrinogen, FBG) adsorption and suppressed platelet adhesion. For the modified membranes, significant decreases in thrombin–antithrombin (TAT) generation, percentage platelets positive for CD62p expression, and the complement activation on C3a and C5a levels were observed compared with those for the pure PES membrane. Due to the similar negatively charged groups as heparin, the modified membranes effectively prolonged the activated partial thromboplastin time (APTT). Furthermore, the modified membranes showed good cytocompatibility. Hepatocytes cultured on the modified materials exhibited improved functional profiles in terms of scanning electron microscope (SEM) observation and 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide (MTT) assay compared with those on the pure PES membrane. It could be concluded that the modified membranes with sulfonic acid and carboxylic acid groups were endowed with excellent biocompatibility, and the heparin-like surface modification seemed to be a promising approach to improve the biocompatibility of materials.

Surface modification of polyethersulfone membrane to improve its hydrophobic characteristics for waste frying oil filtration: Radio frequency plasma treatment

AbstractIn this study, polyethersulfone (PES) membrane was subjected to surface modification using hexamethyldisiloxane (HMDSO) and 1,1,1,3,3,3‐hexafluoro‐2‐propanol (HFIP) in radio frequency (RF) plasma system to improve its hydrophobic property for recovery of waste frying oil. Structural and morphological changes on the membrane surfaces were characterized by contact angle measurements, Fourier transform infrared spectroscopy‐attenuated total reflection (FTIR‐ATR) and atomic force microscopy (AFM). Permeate fluxes, physical and chemical properties of waste frying oil and waste frying oil–methanol micella (oil/methanol 1/3, 1/1, 1/3, v/v) after filtration through unmodified and modified PES membranes were investigated. The results showed that PES membranes modified with HMDSO at 75 W for 5 min (discharge power–exposure time) selectively rejected total polar compounds (TPC) and free fatty acids (FFAs) of waste frying oil to the extent of 46.9–48% and 35.3–40%, respectively. Furthermore, the viscosity of waste frying oil was reduced to the extent of 9.4–12.8%. RF‐plasma‐treated PES membranes appeared to improve the regeneration of waste frying oils and allow these oils to be used for either repeated frying operations or biodiesel production. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci 123:3402–3411, 2012

Biocompatibility of modified polyethersulfone membranes by blending an amphiphilic triblock co-polymer of poly(vinyl pyrrolidone)–b-poly(methyl methacrylate)–b-poly(vinyl pyrrolidone)

An amphiphilic triblock co-polymer of poly(vinyl pyrrolidone)–b-poly(methyl methacrylate)–b-poly(vinyl pyrrolidone) (PVP-b-PMMA-b-PVP) was synthesized via reversible addition–fragmentation chain transfer (RAFT) polymerization. The block co-polymer can be directly blended with polyethersulfone (PES) using dimethylacetamide (DMAC) as the solvent to prepare flat sheet and hollow fiber membranes using a liquid–liquid phase separation technique. The PVP block formed a brush on the surface of the blended membrane, while the PMMA block mingled with the PES macromolecules, which endowed the membrane with permanent hydrophilicity. After adding the as-prepared block co-polymer the modified membranes showed lower protein (bovine serum albumin) adsorption, suppressed platelet adhesion, and a prolonged blood coagulation time, and thereby the blood compatibility was improved. Furthermore, the modified PES membranes showed good cytocompatibility, ultrafiltration and protein anti-fouling properties. These results suggest that surface modification of PES membranes by blending with the amphiphilic triblock co-polymer PVP-b-PMMA-b-PVP allows practical application of these membranes with good biocompatibility in the field of blood purification, such as hemodialysis and bioartificial liver support.

Characterization of Surface Modification of Polyethersulfone Membrane

Surface modification of polyethersulfone (PES) membrane surfaces using UV/ozone pretreatment with subsequent grafting and interfacial polymerization on membrane surface was investigated in order to improve the resistance of membrane surface to protein adsorption. The surface modifications were evaluated in terms of hydrophilicity, chemical composition of the surface and static protein adsorption. In both methods, poly(vinyl alcohol) (PVA), poly(ethylene glycol) (PEG) and chitosan were chosen as hydrophilic polymers to chemically modify the commercial virgin PES membrane to render it more hydrophilic as these materials have excellent hydrophilic property. Modified PES membranes were characterized by contact angle and XPS. Contact angles of modified PES membranes were reduced by 19 to 58% of that of the virgin PES membrane. PES membrane modified with PEG shows higher wettability than other hydrophilic materials with the highest contact angle reduction shown for UV/ozone pretreated, PEG grafted PES membrane surface. In general, XPS spectra supported that the PES membranes were successfully modified by both grafting with UV/ozone pretreatment and interfacial polymerization methods. The results of the static protein adsorption experiments showed all surface modifications led to reduction in protein adsorption on PES membranes; the highest protein adsorption reduction occurred with membrane modified by UV/ozone pretreatment followed by PES grafting, which corresponded to the highest contact angle reduction. However, there seems to be no clear correlation between contact angle reduction and reduction in protein adsorption in the case that involved chitosan. Nevertheless, membranes modified with chitosan do show higher reduction in protein adsorption than membranes modified with other materials under the same conditions.

Novel membranes and surface modification able to activate specific cellular responses

The design of new polymeric biomaterials together with new strategies to modify membrane surface are crucial to optimise cell–biomaterial interactions in vivo and in vitro biohybrid systems. In this study we report on the novel semipermeable membranes synthesised from a polymeric blend of modified polyetheretherketone and polyurethane able to support the long-term maintenance and differentiation of human liver cells and on the surface modification of polyethersulfone membranes by plasma polymerisation of acrylic acid monomers and by immobilization of arginine-glycine-aspartic acid (RGD) peptide through a hydrophilic “spacer arm” molecule. The performance of the modified and unmodified membranes was tested by evaluation of the liver function expression of primary human hepatocytes in terms of albumin production, protein secretion and drug biotransformation.