Physical modification of polymeric support layer for thin film composite forward osmosis membranes by metal–organic framework-based porous matrix membrane strategy

Physical modification of support layers (SLs) for thin-film composite (TFC) forward osmosis (FO) membranes is the main goal of this study. Accordingly, the strategy of metal–organic framework (MOF)-based porous matrix membrane (PMM) was used for the fabrication of controllable SLs. Fourteen different TFC FO membranes were successfully fabricated by interfacial polymerization (IP) technique over the fourteen different SLs made of polyetherimide (PEI), polyethersulfone (PES), and twelve MOF-based PMM. The controllable MOF particles, fabricated SLs, and TFC membranes were characterized by Fourier-transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), dynamic light scattering (DLS), field emission scanning electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), contact angle (CA), inductively coupled plasma (ICP), and developed SHN1 method. The results showed that the PMM strategy can lead to an increase in the degree of crosslinking of polyamide (PA) as a result of physical modification of the original SLs. Also, the PMM strategy reduced the structural parameters and hence the internal concentration polarization (ICP) was controlled. However, according to the characteristic curve, physical modification of the structure of PES and PEI by MOF-based PMM strategy caused a small and dramatic effect (respectively) on the performance of the TFC FO membranes. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 137, 48672.     

Thin film composite membranes with desirable support layer for MeOH/MTBE pervaporation

A comprehensive study was performed on a new application of thin film composite membranes and selecting a stable sublayer for them as pervaporation membranes in organic solvent separation. For this purpose, four different polymeric sublayers of polyethersulfone (PES), cellulose acetate, polyacrylonitrile, and polyetherimide were prepared, and the interaction of methanol (MeOH) and methyl tert butyl ether (MTBE) with them was investigated. The contact angle results, scanning electron microscopy images, and swelling and mechanical strength measurements obviously displayed the effect of immersion in organic solvents on the sublayers. Finally, a polyamide active layer was subsequently deposited on the PES membrane surface as the stable sublayer via interfacial polymerization based on a multistep statistical optimization strategy involving fractional factorial design and a response surface method. The prepared TFC membranes were tested in the pervaporation of a MeOH/MTBE mixture and exhibited excellent performance compared with the current membranes in this context. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47519.     

Structural manipulation of PES constituents to prepare advanced alternative polymer for ultrafiltration membrane

Polyethersulfone (PES) is the most well-known polymer for the preparation of ultrafiltration (UF) membrane, but its membrane suffers from fouling. In this study, two engineered polymers were synthesized to provide optimal antifouling properties for UF membranes that simultaneously benefit from good properties of polyamide and PES. The choice of polyamide is due to its prominent characteristics and the convenience of its synthesis with various functional groups in a cost-effective way. Two hydroxyl containing polyamide bearing sulfone groups (PAS) and ether group (PAE) were synthesized by polycondensation method. The UF membranes were fabricated using the phase inversion method via immersion precipitation of PAS, PAE, and PES in dimethylacetamide, as a solvent and water, as a nonsolvent. The obtained membranes were compared and characterized by means of atomic force microscopy, scanning electron microscopy, contact angle, and Fourier transform infrared spectroscopy in the attenuated total reflection mode. The performance of membranes illustrated that the PAS and PAE membranes in comparison with the PES membrane had better porosity, water permeability, lesser protein fouling, more vertically finger-like pores, and more hydrophilic surface. The water permeability of PES, PAE, and PAS was 7.3, 64.0, and 78.0 L m⁻² h⁻¹ while their flux recovery ratio was 59.4, 83.3, and 86.7%, respectively. The promising permeability and antifouling properties of the PAS are potentially applicable in the efficient industrial separation and wastewater treatment. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 137, 48690.     

Effect of additives concentration on performance of cellulose acetate and polyethersulfone blend membranes

Asymmetric micro porous membranes have been prepared successfully from blending of cellulose acetate (CA) and polyethersulfone (PES) by the phase inversion method with N, N-dimethylformamide (DMF) as solvent. Two additives were selected in this study, including polyethylene glycol 600 (PEG 600) and polyvinylpyrrolidone (PVP). The effects of concentration of additives on CA/PES blend membrane performance and cross-section morphology were investigated in detail. CA/PES membranes were compared with CA/PES/PEG and CA/PES/PVP membranes in the performance such as pure water flux, membrane resistance, porosity and cross-section morphology. The resulting blend membranes were also carried out the rejection and permeate flux of Egg Albumin (EA) proteins with molecular weight of 45 Da. The membranes thus obtained with an additive concentration of 5 wt% of both PEG and PVP exhibited superior properties than the 80/20% blend composition of CA and PES membranes. The permeate flux of protein was increased from 44 to 134 lm² h with increase in concentrations of both PVP and PEG in 80/20% blend composition of CA and PES membranes. Cross-sectional images from scanning electron microscopy showed larger macropores in the bottom layer of the membranes with increasing additives content. Observations from scanning electron microscopy provided qualitative evidence for the trends obtained for permeability and porosity results.     

Improving the hydrophilicity of polyethersulfone membrane by the combination of grafting technology and reverse thermally induced phase separation method

In this work, surface grafting modification technology was combined with reverse thermally induced phase separation (RTIPS) method in order to improve the structure and permanent hydrophilicity of polyethersulfone (PES) membranes. Acrylic solution with different concentrations was grafted on the surface of PES membranes while grafting temperature and grafting time were also varied. The modified PES membranes were characterized in all aspects. Attenuated total reflectance Fourier transform-infrared confirmed successful modification of the PES membrane by grafting acrylic acid. Scanning electron microscopy revealed that homogeneous porous top surface as well as spongy-like cross-section structure appeared in the membrane by RTIPS procedure. Moreover, porosity was affected by changes of acrylic acid concentration, grafting temperature, and grafting time. Atomic force microscopy showed that grafting acrylic acid gave a reduction in roughness of PES membrane. Combined with the decreased values of contact angle, the hydrophilicity and antifouling performance of the PES membrane were improved. The pure water flux and BSA rejection rate of the grafted PES membranes were remarkably improved for pure PES membrane and attained a maximum, which was 1,646.24 L/(m²h) and 94.5%, respectively. The long-term test demonstrated that grafting membranes exhibited outstanding elevated water flux recovery ratio (>85%).     

Hydrophilic goethite nanoparticle as a novel antifouling agent in fabrication of nanocomposite polyethersulfone membrane

The goethite nanoparticle was used as a multifunctional additive to fabricate antifouling polyethersulfone (PES) nanofiltration membranes. The goethite/PES membranes were synthesized via the phase inversion method. The scanning electron microscopy (SEM) photographs showed an increase in pore size and porosity of the prepared membranes with blending of the goethite. The static water contact angle measurements confirmed a hydrophilic modification of the prepared membranes. With increase in the goethite content from 0 to 0.1 wt %, the pure water flux increased up to 12.7 kg/m² h. However, the water permeability decreased using high amount of this nanoparticle. Evaluation of the nanofiltration performance was performed using the retention of Direct Red 16. It was observed that the goethite/PES membranes have higher dye removal capacity (99% rejection) than those obtained from the unfilled PES (89%) and the commercial CSM NE 4040 NF membrane (92%). In addition, the goethite/PES blend membranes showed good selectivity and antifouling properties during long‐term nanofiltration experiments with a protein solution. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43592.     

Effect of solvents on performance of polyethersulfone ultrafiltration membranes: Investigation of metal ion separations

The new polyethersulfone (PES) based ultrafiltration membranes were formed using a two stage process of dry and wet phase inversion in non solvent coagulation bath. The effects of three different solvents such as, N,N-dimethylformamide (DMF), N-methyl-2-pyrrolidone (NMP) and Dimethyl sulphoxide (DMSO) of 82.5% and 85% concentrations on the performance of final membranes were extensively investigated. Scanning electron microscopy (SEM) image results proved that PES membranes with an asymmetric structure were successfully formed. The number of pores formed on the top layer of PES membranes using above-mentioned three solvents was the result of the combined effect of the thermodynamic properties of the system (composition, concentrations, and phase behaviour) and membrane formation kinetics, whereas, the formation of the macroporous sub layer of those membranes was controlled by the diffusion rate of solvent–nonsolvent. The flux of pure water, membrane resistance, mechanical stability, molecular weight cut-off (MWCO) and separation performance of the PES membranes were studied. Separation of metal ions from aqueous solutions was studied for Ni(II), Cu(II) and Cr(III) using two complexing polymer ligands: polyvinyl alcohol (PVA) and poly(diallyldimethylammonium chloride) (PDDA).The separation and permeate rate (flux) efficiencies of the new membranes are compared using different solvents and different PES/solvent compositions.     

Effect of embedding MWCNT-g-GO with PVC on the performance of PVC membranes for oily wastewater treatment

Abstract

In this work, polyvinyl chloride/multi-walled carbon nanotube-grafted-graphene oxide (PVC/MWCNT-g-GO) membranes were fabricated by employing a classical phase inversion method for use in the Al-Dura Refinery (Baghdad, Iraq) wastewater treatment. The effects of MWCNT-g-GO contents on the properties and performance of PVC/MWCNT-g-GO membranes (i.e., 0.0599, 0.119, and 0.219?wt.%) were investigated. Scanning electron microscope (SEM), Fourier-transform infrared spectroscopy (FTIR), atomic force microscopy (AFM), X-ray diffraction (XRD), differential scanning calorimetry (DSC), contact angle (CA), porosity, and mechanical properties were used to characterize the MWCNT-g-GO and composite membranes. The membrane performance was characterized by liquid permeation flux and chemical oxygen demand (COD) rejection. The SEM and AFM results showed significant effects of MWCNT-g-GO on the structural morphology of the membranes. Also, it was found that the addition of a 0.119?wt.% MWCNT-g-GO membrane greatly improved the CA and porosity, from 74.5° to 13.9° and from 69.3% to 81.4%, respectively. Adding 0.219?wt.% of MWCNT-g-GO to the casting solution produced a major positive impact in the membrane mechanical properties. With 0.119?wt.% of MWCNT-g-GO (e.g., 254?L/m²·h), the membrane fostered increases in the water permeation flux that were 66% greater than when using the neat PVC (e.g., 153?L/m²·h). The COD rejection of the prepared membranes also improved significantly, from 60% for neat PVC to 88.9% after adding 0.119?wt.% of MWCNT-g-GO.     

Effect of polymers blend ratio binder on electrochemical and morphological properties of PC/S‐PVC‐based heterogeneous cation‐exchange membranes

In this research, heterogeneous cation exchange membranes were prepared by the casting‐solution technique using polycarbonate (PC) and S‐polyvinylchloride (S‐PVC) as binders along with cation exchange resin as functional group agent. The effect of blend ratio (PC to S‐PVC) of polymer binder on structure and electrochemical properties of the prepared membranes were elucidated. The morphology of the prepared membranes was investigated by scanning electron microscopy (SEM) and scanning optical microscopy (SOM). The images show that the addition of PC ratio in the casting solution results in formation of a membrane with more inner cavities and micro voids. The electrochemical properties and mechanical strength tests were conducted. Water content, ion exchange capacity, ion permeability, flux, current efficiency, and oxidative stability of the prepared membranes initially were decreased by increasing the PC ratio in the casting solution and then it began to increase. The blending of S‐PVC and PC polymers results in membranes with lower mechanical strength. Membrane potential, surface charge density, perm‐selectivity, cationic transport number, electrical resistance, and energy consumption were initially improved by the increment of PC ratio in the casting solution and then it decreased. The membrane with 70% PC exhibited the highest flux, maximum current efficiency, and minimum energy consumption. However, the selectivity of this membrane was low compared with the other prepared membranes. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Synthesis and characterization of PVA/PES thin film composite nanofiltration membrane modified with TiO2 nanoparticles for better performance and surface properties

Novel polyethersulfone (PES)/poly (vinyl alcohol) (PVA)/titanium dioxide (TiO₂) composite nanofiltration membranes were prepared by dip-coating of PES membrane in PVA and TiO₂ nanoparticles aqueous solution. Glutaraldehyde (GA) was used as a cross-linker for the composite polymer membrane in order to enhance the chemical, thermal as well as mechanical stabilities. TiO₂ nanoparticles with different concentrations (0, 0.05, 0.1, 0.5 wt.%) were coated on the surface of PVA/PES composite membrane. The morphological study was investigated by atomic force microscopy (AFM), scanning surface microscopy (SEM) and along with X-ray diffraction (XRD). In addition, the membranes performances, in terms of permeate flux, ion rejection and swelling factor were also investigated. It was found that the increase in TiO₂ solution concentration can highly affect the surface morphology and filtration performance of coated membranes. The contact angle measurement and XRD studies indicated that the TiO₂ nanoparticles successfully were coated on the surface of PVA/PES composite membranes. However, rougher surface was obtained for membranes by TiO₂ coating. The filtration performance data showed that the 0.1 wt.% TiO₂-modified membrane presents higher performance in terms of flux and NaCl salt rejection. Finally, TiO₂ modified membranes demonstrated the lower degree of swelling.     

Preparation and Characterization of pH-Sensitive Polyethersulfone Membranes Blended with Poly(methyl methacrylate-co-maleic anhydride) Copolymer

The current study aims to endow polyethersulfone (PES) hollow fiber membranes (HFMs) with improved pH-sensitivity by blending a random copolymer of poly(methyl methacrylate-co-maleic anhydride) (P(MMA-MA)). It was found that PES membrane modified by random copolymer had more obvious pH-sensitivity than those by alternative copolymer; while low molecular weight copolymer modified PES membrane had no pH-sensitivity. P(MMA-MA) was synthesized by a controlled dosing method via free radical polymerization and characterized by Fourier transform infrared spectroscopy (FTIR) analysis, nuclear magnetic resonance (¹H NMR), elemental analysis, gel permeation chromatography technique (GPC), and differential scanning calorimetry (DSC) measurement. Scanning electron microscopy (SEM) was used to investigate the morphology of the HFMs. The modified HFMs showed excellent pH-sensitivity, pH-reversibility and hysteresis of water flux. Through the ultrafiltration of PEG solution, we investigated the pore size change and the electroviscous effect on the water flux of the modified HFMs. Meanwhile, the modified membranes were stable with respect to the mechanical force (pressure) and exhibited good ability of Cu²⁺ adsorption.     

Effect of hypochlorite treatment on performance of hollow fiber membrane prepared from polyethersulfone/N‐methyl‐2‐pyrrolidone/tetronic 1307 solution

Polyethersulfone (PES) hollow fiber membrane was prepared by blending with nonionic surfactant Tetronic 1307 to improve its hydrophilicity. The membranes were posttreated by hypochlorite solution of 10, 100, 500, and 2000 ppm. The effect of hypochlorite treatment on the performance of PES membrane was investigated. Experimental results showed that the water permeability of treated membrane was two to three times higher than that of untreated membrane in case of blend membrane prepared from PES/N‐methyl‐2‐pyrrolidone (NMP)/Tetronic 1307 solution. On the other hand, hypochlorite treatment has no effect on water permeability of the membrane prepared from PES/NMP solution. Elemental analysis and ATR–FTIR measurement results indicated that hypochlorite treatment led to decomposition and leaching out of Tetronic 1307 component from the membrane. The change of membrane surface structure by the hypochlorite treatment was confirmed by atomic force microscopy measurement. The hypochlorite treatment brought about no significant impact on the mechanical property of the membranes. This indicated that the hypochlorite treatment of PES membrane prepared with surfactant was a useful way to improve the water permeability without the decrease of membrane strength. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Poly(vinyl chloride) hollow‐fiber membranes for ultrafiltration applications: Effects of the internal coagulant composition

Poly(vinyl chloride) (PVC) hollow‐fiber membranes were spun by a dry/wet phase‐inversion technique from dopes containing 15 wt % PVC to achieve membranes with different pore sizes for ultrafiltration (UF) applications. The effects of the N,N‐dimethylacetamide (DMAc) concentration in the internal coagulant on the structural morphology, separation performance, and mechanical properties of the produced PVC hollow fibers were investigated. The PVC membranes were characterized by scanning electron microscopy, average pore size, pore size distribution, void volume fraction measurements, and solubility parameter difference. Moreover, the UF experiments were conducted with pure water and aqueous solutions of poly(vinyl pyrrolidone) as feeds. The mechanical properties of the PVC hollow‐fiber membranes were discussed in terms of the tensile strength and Young's modulus. It was found that the PVC membrane morphology changed from thin, fingerlike macrovoids at the inner edge to fully spongelike structure with DMAc concentration in the internal coagulant. The effective pores showed a wide distribution, between 0.2 and 1.1 μm, for the membranes prepared with H₂O as the internal coagulant and a narrow distribution, between 0.114 and 0.135 μm, with 50 wt % DMAc. The results illustrate that the difference in the membrane performances was dependent on the DMAc concentration. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Influence of hydroxyl‐terminated polybutadiene additives on the poly(ether sulfone) ultra‐filtration membranes

Hydroxyl‐terminated polybutadiene (HTPB) was blended into a poly(ether sulfone) (PES) casting solution used to prepare ultra‐filtration (UF) membranes via the phase inversion technique. The membranes were then characterized by contact angle (CA) measurements and UF experiments. The CA was increased with the addition of HTPB in the PES membrane and also by lowering the gelation bath temperature. It was observed that the CA was lower for membranes prepared with N‐methyl‐2‐pyrrolidinone (NMP) as the solvent than those using N,N‐dimethylacetamide (DMAc) as solvent. The flux values were higher for membranes made using a 4°C gelation bath when compared with the ambient temperature ((25 ± 1)°C) irrespective of the cast solvents, NMP or DMAc. The flux values were much higher and the solute separations were lower for the HTPB‐based PES membranes than for the pure PES membrane, when the membranes were cast with DMAc as a solvent. On the other hand, both flux and separation values were much lower for the HTPB‐based PES membranes than for the pure PES membrane, when the membranes were cast using NMP. Atomic force microscopy and scanning electron microscopy were used for morphological characterization and the correlation of topography/photography with the performance data was also examined. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2292–2303, 2006     

Polyethersulfone composite hollow-fiber membrane prepared by in-situ growth of silica with highly improved oily wastewater separation performance

In order to reduce surface aggregation and enhance the performance of PES membranes, a hydrophilic PES/TEOS HF membrane was developed for the treatment of wastewater containing oil. PES/TEOS was prepared via a sol-gel self assembly and dry–wet spinning method. Silicon dioxide sol was prepared from a mixture of tetraethoxysilane, ethanol, water, and acetic acid (acting as the catalyst). HF hybrid membranes were produced from dope solutions containing polyethersulfone, polyethylene glycol, silicon sol, and NMP. The membranes were characterized by field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), energy-dispersive X-ray spectroscopy (EDX), porosity, fourier transform infrared spectroscopy (FTIR), and contact angle measurements. The composite membranes were successfully used to treat wastewater containing oil and their separation performance were evaluated. The PES/TEOS-2 membrane displayed the best performance, with a permeate flux of 90.937 L/m² h and an oil retention of 99.98%. In addition, this membrane showed a higher pure water flux of 102.43 L/m² h as compared to PES-0 and PES/SiO₂–1 membranes (87.347 L/m² h and 91.949 L/m² h, respectively). The PES/TEOS-2 membrane also presented enhanced antifouling behavior with a FRR and a RFR of 93.33% and 11.22%, respectively. In addition, this membrane displayed excellent long-term recycling properties, making it a desirable candidate for oily wastewater separation applications.     

Super-hydrophilic electrospun PVDF/PVA-blended nanofiber membrane for microfiltration with ultrahigh water flux

This work provides a novel approach to improve not only water flux but also fouling resistance of Polyvinylidene fluoride (PVDF) membranes. PVDF/Poly(vinyl alcohol) (PVA)-blended nanofiber membranes were prepared via electrospinning method. The structure and performance of blended nanofiber membranes were characterized by scanning electron microscopy (SEM), atomic force microscope (AFM), attenuated total reflection-Fourier-transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), contact angle measurement, tensile mechanical measurement, and filtration experiments. These results indicate that PVA was uniformly blend in the PVDF matrix. This blended nanofiber membranes with the ridge-and-valley structure and bicontinuous phase exhibited the hydrophilic performance and super-wettability, which is reflected in a drop of water fully spread within 1.44 s. Filtration experiments showed that the blended nanofiber membranes have ultrahigh flux and low irreversible fouling ratio. In general, this work enhances the possibility of hydrophilic modification of hydrophobic PVDF membranes. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48416.     

Significance of thermodynamics and rheological characteristics of dope solutions on the morphological evolution of polyethersulfone ultrafiltration membranes

Herein, the effect of solvent type and polymer concentration on the thermodynamic and viscoelastic properties, and performance of polyethersulfone (PES) ultrafiltration (UF) membranes are investigated. The morphology and mechanical properties of the membranes are examined too. Rheological measurements indicated that solidification and instantaneous demixing occurred fast for PES/N-methyl-2-pyrrolidone (NMP) dope solution. This resulted in a dense skin layer with a finger-like structure confirmed by the scanning electron microscopy images. In comparison, PES/dimethylformamide (DMF) exhibited a delayed solidification and demixing with a sponge-like structure. Rheological characteristics and ternary phase diagrams of two systems are examined to gain insights and make correlations with the morphology of resultant membranes. Performance analysis revealed that membranes derived from PES/NMP system exhibited both improved pure water flux and bovine serum albumin rejection suggesting the superiority of NMP compared to DMF as the solvent of choice for the preparation of PES UF membranes.     

An Efficient Preparation and Characterization of Nanocomposite Films Based on Poly(vinyl chloride) and Modified ZnO Quantum Dot with an Optically Active Diacid Containing Amino Acid as Coupling Agent

The nanocomposites were manufactured by the incorporation of modified ZnO into the poly(vinyl chloride). ZnO nanoparticles were modified with diacid containing alanine amino acid. Ultrasonic irradiation was used for all process. The PVC/ZnO@DA nanocomposites were investigated by field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, UV–visible spectroscopy, thermogravimetric, and mechanical analysis. Results showed the uniform dispersion of particles in the polymer matrix and ZnO@DA nanoparticles in quantum dot size. The optical properties of PVC were affected by the incorporation of modified quantum dot ZnO; also mechanical properties of PVC/ZnO@DA nanocomposites were improved.     

Effect of polyethylene glycol molecular weights and concentrations on polyethersulfone hollow fiber ultrafiltration membranes

Polyethersulfone (PES) hollow‐fiber membranes were fabricated using poly(ethyleneglycol) (PEG) with different molecular weights (MW = PEG200, PEG600, PEG2000, PEG6000, and PEG10000) and poly(vinyl pyrrolidone) PVP40000 as additives and N‐methyl‐2‐pyrrolidone (NMP) as a solvent. Asymmetric hollow‐fiber membranes were spun by a wet phase‐inversion method from 25 wt % solids of 20 : 5 : 75 (weight ratio) PES/PEG/NMP or 18 : 7 : 75 of PES/(PEG600 + PVP40000)/NMP solutions, whereas both the bore fluid and the external coagulant were water. Effects of PEG molecular weights and PEG600 concentrations in the dope solution on separation properties, morphology, and mechanical properties of PES hollow‐fiber membranes were investigated. The membrane structures of PES hollow‐fiber membranes including cross section, external surface, and internal surface were characterized by scanning electron microscopy and the mechanical properties of PES hollow‐fiber membranes were discussed. Bovine serum albumin (BSA, MW 67,000), chicken egg albumin (CEA, MW 45,000), and lysozyme (MW 14,400) were used for the measurement of rejection. It was found that with an increase of PEG molecular weights from 200 to 10,000 in the dope solution, membrane structures were changed from double‐layer fingerlike structure to voids in the shape of spheres or ellipsoids; moreover, there were crack phenomena on the internal surfaces and external surfaces of PES hollow‐fiber membranes, pure water permeation fluxes increased from 22.0 to 64.0 L m^?2 h^?1 bar^?1, rejections of three protein for PES/PEG hollow‐fiber membranes were not significant, and changes in mechanical properties were decreased. Besides, with a decrease of PEG600 concentrations in the dope solution, permeation flux and elongation at break decreased, whereas the addition of PVP40000 in the dope solution resulted in more smooth surfaces (internal or external) of PES/(PEG600 + PVP40000) hollow‐fiber membranes than those of PES/PEG hollow‐fiber membranes. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3398–3407, 2004     

Polyethersulfone/Poly(D,L‐lactide) Blend Membranes: Preparation,Characterization, and Performance

Polyethersulfone (PES) was blended with poly(D,L‐lactide) (PDLLA) to prepare asymmetric membranes using the phase inversion method. The effects of the blend ratios and poly(ethylene glycol) (PEG) as additive on the membrane structure, properties, and performance were investigated. The membranes were characterized by contact angle determination, scanning electron microscopy, porosity measurement, thermogravimetric analysis, degradation tests in compost, and dynamic tests for pure water flux and bakery product wastewater treatment. PES and PEG slightly reduced the membrane contact angle. Increasing the PDLLA concentration in the blend membranes enhanced the membrane degradation in compost and also the membrane porosity. The permeate flux of the membranes was improved, but the rejection of pollution indices did not change noticeably.