Amphiphilic PVDF-g-PDMAPMA ultrafiltration membrane with enhanced hydrophilicity and antifouling properties

It is easy to adsorb the pollutants from water owning to the hydrophobicity of the poly(vinylidene fluoride) (PVDF) ultrafiltration (UF) membrane. To improve the hydrophilicity of the PVDF UF membrane, a novel amphiphilic copolymer PVDF-g-poly-N-(3-dimethylaminopropyl)methacrylamide] (PDMAPMA) was developed. The amphiphilic PVDF-g-PDMAPMA was synthesized with PVDF and N-(3-dimethylaminopropyl)methacrylamide (DMAPMA) via free-radical polymerization, and characterized by Fourier transform infrared spectroscopy and ¹H nuclear magnetic resonance. The scanning electron microscopy and energy dispersive X-ray spectroscopy were used to characterize the structure morphologies and elementals of the blend PVDF membranes, respectively. The pure water flux (PWF), molecular weight cutoff, and bovine serum albumin (BSA) solution filtration experiments were tested to evaluate the permeation performance and antifouling properties of the membranes. The experimental results showed that the PWF was 263.1 L m⁻² h⁻¹, BSA rejection rate was 98.1% and flux recovery rate was 95.1% of the prepared blend membrane which had obvious improvement compared with the pristine PVDF membrane (17.3 L m⁻² h⁻¹, 91.0, and 83.8%, respectively). The antibacterial activity test showed the prepared blend membrane had good potency against microorganisms. A novel hydrophilic PVDF membrane with good antibacterial properties was developed and would be promising for wastewater treatment. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48049.     

Poly(ether imide) membranes modified with charged surface‐modifying macromolecule—Its performance characteristics as ultrafiltration membranes

Modification of poly (ether imide) (PEI) ultrafiltration (UF) membranes was attempted by blending charged surface modifying macromolecule (cSMM). Compared to the pure PEI membrane, blending of PEI with cSMM resulted in blend membranes with enhanced UF characteristics such as lower hydraulic resistance (R_m) and higher pure water flux (PWF) coupled with higher water content (WC). Among the various modified membranes, blend membranes with 5 wt % cSMM concentration exhibited higher PWF (60.38 L m^?2 h^?1), WC (73.6%), protein permeate flux (27.12 L m^?2 h^?1) and lower flux decline rate (R_fd) (55.1%), R_m (5.21 kPa/L m^?2 h^?1), bovine serum albumin (BSA) rejection (87.1%). Meanwhile, the fouling resistant ability was studied by flux recovery ratio (FRR) after water and alkali cleaning, irreversible and reversible fouling rate. Higher FRR after water cleaning (95.07%), FRR after alkali cleaning (97.1%), reversible fouling rate (50.14%) and lower irreversible fouling rate (5%) exhibited by 5 wt % cSMM membranes showed its better antifouling ability compared to pure PEI and other blend membranes because of its higher hydrophilic nature. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40320.     

Preparation of PVDF/poly(tetrafluoroethylene‐co‐vinyl alcohol) blend membranes with antifouling propensities via nonsolvent induced phase separation method

Poly(vinylidene fluoride) (PVDF) was blended with a new amphiphilic copolymer, poly(tetrafluoroethylene‐co‐vinyl alcohol) [poly(TFE‐VA)], via non‐solvent induced phase separation (NIPS) method to make membranes with superior antifouling properties. The effects of the VA/TFE segment ratio of the copolymer and the copolymer/PVDF blend ratio on the properties of the prepared membranes were studied. Membranes with similar water permeabilities, surface pore sizes, and rejection properties were prepared and used in bovine serum albumin (BSA) filtrations with the same initial water flux and almost the same operating pressure, to evaluate the sole effect of membrane material on fouling propensity. While the VA/TFE segment ratio strongly affected the membrane antifouling properties, the effects of the copolymer/PVDF blending ratio were not so drastic. Membrane surface hydrophilicity increased, and BSA adsorption and fouling decreased upon blending a small amount of amphiphilic copolymer with a high VA/TFE segment ratio with PVDF (copolymer/PVDF blending ratio 1:5). © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43780.     

Amphiphilic ABA‐type triblock copolymers for the development of high‐performance poly(vinylidene fluoride)/poly(vinyl pyrrolidone) blend ultrafiltration membranes for oil separation

ABA‐type amphiphilic triblock copolymers (TBCs) were synthesized by a reversible addition fragmentation chain transfer (RAFT) process with a telechelic polystyrene macro‐RAFT agent and 4‐[n‐(acryloyloxy)alkyloxy]benzoic acid monomers. Ultrafiltration (UF) membranes were fabricated by a phase‐inversion process with blends of the TBC, poly(vinylidene fluoride) (PVDF), and poly(vinyl pyrrolidone) (PVP) in dimethylformamide. The UF‐fabricated membranes were characterized by scanning electron microscopy, atomic force microscopy, water contact angle measurement, thermogravimetric analysis, and differential scanning calorimetry. Pure water permeation, molecular weight cutoff values obtained by the permeation of different molecular weight polymers as probe solutes, bovine serum albumin (BSA) solution permeate flux, and oil–water emulsion filtration tests were used to evaluate the separation characteristics of the fabricated membranes. The tripolymer blend membranes exhibited a higher flux recovery ratio (FRR) after the membrane was washed with sodium lauryl sulfate (0.05 wt %) solution for a BSA solution (FRR = 88%) and oil–water emulsion (FRR = 95%) feeds when than the PVDF–PVP blend membrane (57 and 80% FRR values for the BSA solution and oil–water emulsion, respectively). The pendant carboxylic acid functional moieties in this ABA‐type TBC have potential advantages in the fabrication of high‐performance membranes. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45132.     

Poly(vinylidene fluoride) hollow‐fiber membranes containing silver/graphene oxide dope with excellent filtration performance

In this study, an antifouling poly(vinylidene fluoride) (PVDF) hollow‐fiber membrane was fabricated by blending with silver‐loaded graphene oxide via phase inversion through a dry‐jet, wet‐spinning technique. The presence of graphene oxide endowed the blended membrane with a high antifouling ability for organic fouling. The permeation fluxes of the blended membrane was 3.3 and 2.9 times higher than those of a pristine PVDF membrane for filtering feed water containing protein and normal organic matter, respectively. On the other hand, the presence of silver improved the antibiofouling capability of the blended membrane. For the treatment of Escherichia coli suspension, the permeation flux of the blended membranes was 8.2 times as high as that of the pristine PVDF membrane. Additionally, the presented blended membrane improved the hydrophilicity and mechanical strength compared to those of the pristine PVDF membrane, with the water contact angle decreasing from 86.1 to 62.5° and the tensile strength increasing from 1.94 to 2.13 MPa. This study opens an avenue for the fabrication of membranes with high permeabilities and antifouling abilities through the blending of graphene‐based materials for water treatment. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44713.     

Antifouling poly(vinylidene fluoride) hollow fiber membrane with hydrophilic surfaces by ultrasonic wave‐assisted graft polymerization

Acrylic acid (AA)‐grafted poly(vinylidene fluoride) (PVDF) hollow fiber membrane was obtained by ultrasonic wave‐assisted graft polymerization. The grafting density (GD) of AA on the PVDF membrane surface could be controlled by altering the reaction conditions, such as ultrasonic time, ultrasonic power, monomer concentration and initiator concentration. The attenuated total reflectant Fourier transform infrared spectra (FITR‐ATR) and X‐ray photoelectron spectroscopy were used to investigate the chemical composition of modified membranes. The changes of surface morphology and roughness were characterized by field emission scanning electron microscope and atomic force microscopy. Results show that AA was successfully grafted on the membrane surface. With increasing GD, the static water contact angle was decreased from 95.7 to 41.4°, indicating that hydrophilicity of modified membrane was significantly enhanced. Pure water flux before and after bovine serum albumin (BSA) contamination was measured. The modified membrane with the GD of 0.76 mg/cm² has the highest water flux as high as 350 L/m²·h. When compared with the pristine membrane(M0), the flux recovered ratio was improved from 52.75 to 96.29% at the GD 2.76 mg/cm² (M3), which suggested the protein fouling could be effectively prevented for the modified membrane. POLYM. ENG. SCI., 2018. © 2018 Society of Plastics Engineers POLYM. ENG. SCI., 59:E446–E454, 2019. © 2018 Society of Plastics Engineers     

Enhanced PVDF membrane performance via surface modification by functional polymer poly(N-isopropylacrylamide) to control protein adsorption and bacterial adhesion

The aim of this work is to prepare antifouling membrane with low-biofouling property by grafted functional polymer. Surface modification of poly(vinylidene fluoride) (PVDF) membrane was carried out via a modified and simple process by grafted poly(N-isopropylacrylamide) (PNIPAAm). The grafting density of PNIPAAm was significantly improved, up to 0.90 ± 0.38 mg/cm², thereby improving the properties and performance of the membrane. The chemical composition, thermal stability and surface morphology of pristine and modified membranes had been characterized by attenuated total reflectance fourier-transform infrared spectroscopy (ATR-FTIR), thermo-gravimetric analysis (TGA), scanning electron microscopy (SEM) and atomic force microscope (AFM), respectively. After modification, the hydrophilicity of PVDF membrane was dramatically enhanced due to incorporation of PNIPAAm chains. The results of protein adsorption, microfiltration experiments and bacterial adhesion test demonstrated that the modified membrane exhibited obvious thermo-sensitive property and good antifouling capability. The maximum of flux recovery ratio (FRR), 91.59%, was obtained for the modified membrane. It is evidently believed that protein foulants was removed easily from the modified membrane surface after water washing. In addition, bacterial adhesion test revealed that the attachment of Escherichia coli on the modified membrane was reduced by 75% compared to the original membrane.     

Cellulose acetate ultrafiltration membranes customized with copper oxide nanoparticles for efficient separation with antifouling behavior

Cellulose acetate (CA) nanocomposite ultrafiltration membranes are fabricated with copper oxide (CuO) nanoparticles with the aim of improving efficient protein separation and antifouling performance. CuO nanoparticles are synthesized from cupric nitrate using a wet precipitation method and characterized by FTIR and XRD. CA/CuO nanocomposite membranes fabricated using 0.5, 1.0, and 1.5 wt% of CuO nanoparticles individually by simple phase inversion technique. The CA nanocomposite membrane with 0.5 wt% of hydrophilic CuO exhibited enhanced PWF of 118.6 Lm⁻² h⁻¹ due to the improvement in porosity and water uptake. This is in good agreement with the enhanced hydrophilicity of the CA/CuO nanocomposite membranes results observed in surface contact angle and morphological investigations. Further, 95.5% of BSA separation and 94.7% of flux recovery ratio (FRR) indicates its superior antifouling potential caused due to the presence of the hydration layer at the CA/CuO membrane surface. Among all the fabricated membranes, the CA-0.5 nanocomposite membrane with 0.5 wt% of CuO exhibited superiorly improved hydrophilicity, water permeation, BSA separation, and antifouling performance indicates its potential use in water and wastewater treatment applications.     

Synthesis of well‐defined amphiphilic block copolymers via AGET ATRP used for hydrophilic modification of PVDF membrane

A well‐defined amphiphilic block copolymer consisting of a hydrophobic block poly(methyl methacrylate) (PMMA) and a hydrophilic block poly[N,N–2‐(dimethylamino) ethyl methacrylate] (PDMAEMA) was synthesized by activator generated by the electron transfer for atom transfer radical polymerization method (AGET ATRP). Kinetics study revealed a linear increase in the graph concentration of PMMA‐b‐PDMAEMA with the reaction time, indicating that the polymer chain growth was consistent with a controlled process. The gel permeation chromatography results indicated that the block copolymer had a narrow molecular weight distribution (Mw/Mn = 1.42) under the optimal reaction conditions. Then, poly(vinylidene fluoride) (PVDF)/PMMA‐b‐PDMAEMA blend membranes were prepared via the standard immersion precipitation phase inversion process, using the block copolymer as additive to improve the hydrophilicity of the PVDF membrane. The presence and dispersion of PMMA‐b‐PDMAEMA clearly affected the morphology and improved the hydrophilicity of the as‐synthesized blend membranes as compared to the pristine PVDF membranes. By incorporating 15 wt % of the block copolymer, the water contact angle of the resulting blend membranes decreased from pure PVDF membrane 98° to 76°. The blend membranes showed good stability in the 20 d pure‐water experiment. The bovine serum albumin (BSA) absorption experiment revealed a substantial antifouling property of the blend membranes in comparison with the pristine PVDF membrane. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42080.     

Facile surface modification of PVDF microfiltration membrane by strong physical adsorption of amphiphilic copolymers

To endow the surface of poly(vinylidene fluoride) (PVDF) microfiltration (MF) membranes with hydrophilicity and antifouling property, physical adsorption of amphiphilic random copolymers of poly(ethylene glycol) methacrylate (PEGMA) and poly(methyl methacrylate) (PMMA) (P(PEGMA‐r‐MMA)) onto the PVDF membrane was performed. Scanning electron microscopy (SEM) images showed that the adsorption process had no influence on the membrane structure. Operation parameters including adsorption time, polymer concentration, and composition were explored in detail through X‐ray photoelectron spectroscopy (XPS), static water contact angle (CA), and water flux measurements. The results demonstrated that P(PEGMA‐r‐MMA) copolymers adsorbed successfully onto the membrane surface, and hydrophilicity of the PVDF MF membrane was greatly enhanced. The antifouling performance and adsorption stability were also characterized, respectively. It was notable that PVDF MF membranes modified by facile physical adsorption of P(PEGMA₅₈‐r‐MMA₃₃) even showed higher water flux and better antifouling property than the commercial hydrophilic PVDF MF membranes. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3112–3121, 2013     

Surface modification of polyamide reverses osmosis membrane by phosphonic acid group with improved performance

A facial method for preparing reverse osmosis polyamide (PA) membranes of excellent antifouling and separation performance was developed via covalently grafting phosphonic acid on membrane surface. First, a pristine PA layer was synthesized by interfacial polymerization between m-phenylenediamine and trimesoyl chloride. Then, a second interfacial reaction was implemented between ethylenediamine and the residual acryl chloride on the pristine PA layer, generating an active layer enriched by primary amine. Finally, the amine-rich surface treated by formaldehyde and phosphorous acid to produce a membrane surface modified by phosphonic acid groups. Surface characterization by attenuated total reflectance infrared, X-ray photoelectron spectroscopy and zeta-potential measurements illustrated the presence of phosphonic acid group. The lowest contact angle of modified membrane was 26°, demonstrating the membrane possessed an outstandingly wettable surface. The optimal separation performance was 88 L m⁻² h⁻¹ of water flux and 99.4% of salt rejection under 1.55 MPa. In addition, bovine serum albumin was used as organic foulant to measure the antifouling property of membranes. The result of dynamic fouling experiments indicated that the modified membrane exhibited better antifouling (of which the irreversible fouling degree was 7.1%) compared with commercial membrane BW30 (of which the irreversible fouling degree was 13.5%). © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 46931.     

Asymmetric membranes fabricated from poly(acrylonitrile‐co‐N‐vinyl‐2‐pyrrolidone)s with excellent biocompatibility

Poly(acrylonitrile‐co‐N ‐vinyl‐2‐pyrrolidone)s (PANCNVPs) show excellent biocompatibility. In this work, PANCNVPs with different contents of N‐vinyl‐2‐pyrrolidone (NVP) were fabricated into asymmetric membranes by the phase inversion method. The surface chemical composition of the resultant membranes was determined by Fourier transform infrared spectroscopy–attenuated total reflection. Field emission scanning electron microscopy was used to examine the surface and cross section morphologies of the membranes. It was found that the morphologies hardly change with the increase of NVP content in PANCNVP, while the deionized water flux increases remarkably and the bovine serum albumin (BSA) retention decreases slightly. Experiment of dynamic BSA solution filtration was carried out to evaluate the antifouling properties of the studied membranes. The relative flux reduction of PANCNVP membrane containing 30.9 wt % of NVP is 25.9%, which is far smaller than that of the polyacrylonitrile membrane (68.8%). Results deduce that this improvement comes from the excellent biocompatibility of NVP moieties instead of the hydrophilicity change, because the water contact angles of these membranes fluctuate between 60 and 70°. Results from the membranes using poly(N‐vinyl‐2‐pyrrolidone) (PVP) as an additive confirm that, to a certain extent, the PANCNVP membranes show the advantages of antifouling compared with the polyacrylonitrile/PVP blending membrane. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4577–4583, 2006     

Performance evaluation of polyvinylchloride/polyacrylonitrile ultrafiltration blend membrane

Polyvinylchloride (PVC) membranes were modified by blending with polyacrylonitrile (PAN) as a second polymer. The miscibility of PVC/PAN blend was examined using an incompressible regular solution (CRS) model in no need to make a membrane. The results showed that the PVC/PAN blend was immiscible for all compositions at a temperature range of ?25 to 225 °C. Furthermore, the prediction of the phase behavior of a PVC/PAN/DMF ternary system showed that the blend of two polymers was highly incompatible even in their common DMF solvent. However, this incompatibility led to a remarkable increase in the porosity of the blend membrane and pure water flux compared to those for pure PVC membrane. The pure water flux of the PVC membrane (37.9 ± 1.5 L/m² h) increased about 41 and 76% by adding 10 and 20 wt% PAN, respectively. The blend membranes also showed an enhanced flux recovery ratio (FRR) compared to a pure PVC membrane, although the PVC membrane rejection for Bovine serum albumin (BSA) was decreased after blending with PAN. The PVC/PAN (90/10) blend membrane was subjected to hydrolysis with NaOH alkaline solution at three different concentrations and contact times to further enhance its performance. The membrane, which was hydrolyzed with a 0.5 mol/L NaOH solution for 0.5 h, showed a highest pure water flux of 75.6 ± 7.2 L/m² h due to its increased hydrophilicity. This membrane also revealed an improved FRR and better thermal and mechanical properties compared to an unmodified membrane.     

Preparation and application of zinc oxide/poly(m-phenylene isophthalamide) hybrid ultrafiltration membranes

A small molecular-weight cut-off (MWCO) of 6000 Da poly(m-phenylene isophthalamide) (PMIA) embedded zinc oxide (ZnO) hybrid ultrafiltration (UF) membrane was synthesized via nonsolvent-induced phase separation (NIPS). Tests of field emission scanning electron microscope (FE-SEM), energy dispersive X-ray spectroscopy (EDX), atomic force microscopy (AFM), thermal gravimetric analyzer (TGA), Fourier transform infrared (FTIR), capillary flow porometer (CPF), mechanical test, and pure water flux (PWF) for characterization of membranes were carried out. The EDX, FTIR, and TGA indicated the presence of ZnO in the polymer matrix. The hybrid membranes showed enhanced pore density, PWF by the presence of the particles. The contact angle and water flux of modified membrane with 0.03 wt % of nano-ZnO were 47.7° and 52.58 L·m⁻²·h⁻¹ compared to 71.6° and 36.27 L·m⁻²·h⁻¹ respectively; Compared with the hydrophobic membrane, the PMIA membrane, with hydrophilicity, is supposed to exhibit good antifouling properties. Furthermore, the thermal stability and mechanical properties of the modified membranes were increased. Finally, the hybrid membrane was used in treating papermaking white wastewater and exhibited good separation and high water flux. The great properties of the ultrafiltration PMIA membranes indicate their potential for excellent performance in industrial applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47583.     

Poly(arylene sulfide sulfone) hybrid ultrafiltration membrane with TiO2‐g‐PAA nanoparticles: Preparation and antifouling performance

Poly(arylene sulfide sulfone) (PASS) is a kind of newly developed polymeric membrane material which has excellent mechanical strength, thermal stability, and solvent resistance. And, it would be a potential material for high temperature ultrafiltration and organic solvent filtration. In this article, PASS hybrid ultrafiltration membrane with improved antifouling property was prepared by mixing TiO₂ nanoparticles which were grafted with polyacrylic acid (PAA). These membranes were prepared by a phase inversion technique and their separation performance and antifouling property of the prepared membranes were investigated in detail by SEM, FTIR, EDS, contact angle goniometry, filtration experiments of water, and BSA solution. The results shown that the TiO₂‐g‐PAA nanoparticles dispersed well in membrane matrix, the hydrophilicity of the membranes prepared within TiO₂‐g‐PAA nanoparticles have been improved and these membranes exhibited excellent water flux and antifouling performance in separation than that of the pure PASS membranes and PASS membranes with TiO₂ nanoparticles. More specifically, among membrane sample M0, M1.5, and MP1.5, MP1.5 which contained 1.5 wt% TiO₂‐g‐PAA exhibited the highest water permeation (190.4 L/m² h at 100 kPa), flux recovery ratio, and the lowest BSA adsorption amount. POLYM. ENG. SCI., 55:2829–2837, 2015. © 2015 Society of Plastics Engineers     

Structural and performance properties of UV-assisted TiO2 deposited nano-composite PVDF/SPES membranes

In this research, the surface of poly (vinylidene fluoride) (PVDF)/sulfonated polyethersulfone (SPES) blend membrane prepared via immersion precipitation was modified by depositing of TiO₂ nano-particles followed by UV irradiation to activate their photocatalytic property. The membranes were characterized by FTIR, SEM, AFM, contact angle, dead end filtration (pure water flux and BSA solution flux), antifouling analysis and antibacterial activity. The FTIR spectrum confirmed the presence of OH functional groups on the PVDF/SPES membrane structure, which was the key factor for deposition, and self-assembly of TiO₂ nanoparticles on the membrane surface. The SEM and AFM images indicated that the TiO₂ nanoparticles were deposited on the PVDF/SPES membrane. The contact angle measurements showed that the hydrophilicity of PVDF/SPES membrane was strongly improved by TiO₂ deposition and UV irradiation. The filtration results indicated that the initial flux of TiO₂ deposited PVDF/SPES membranes was lower than the initial flux of neat PVDF/SPES membrane. However, the former membranes showed lower flux decline compared to the neat PVDF/SPES membrane. The BSA rejection of modified membranes was improved. The fouling analysis demonstrated that the TiO₂ deposited PVDF/SPES membranes showed the fewer tendencies to fouling. The results of antibacterial study showed that the UV irradiated TiO₂ deposited PVDF/SPES membranes possess high antibacterial property.     

Role of poly(2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid) in the modification of polysulfone membranes for ultrafiltration

In this study polysulfone membranes with antifouling and hydrophilic properties were synthesized using poly(2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid) (AMPS) as an additive for the first time. Different wt % of AMPS was used to prepare polysulfone membranes by phase inversion method. The role of AMPS on the porosity, pore size distribution, hydrophilicity, and antifouling nature was investigated and analyzed in detail. Characterization techniques like field emission scanning electron microscope, atomic force microscopy, and imageJ software were used to characterize the morphology of prepared membranes. There is positive effect of the additive addition on all the membrane parameters like Pure water flux [101.76 L/(m² h)] (MR0) to 464.06 L/(m² h) (MR4)], hydraulic permeability [0.65 (MR0) to 2.01 (MR4)], equilibrium water content [21.74 (MR0) to 71.45 (MR4)], and porosity [0.024 (MR0) to 0.58 (MR4)]. Response surface methodology was used for the optimization of bovine serum albumin (BSA) flux and rejection. The results of the morphological as well as permeation studies depicted that permeate flux and antifouling nature were increased with the amount of AMPS present in the membrane matrix. The antifouling study of the prepared membranes was undertaken by using BSA solution of 1000 mg/L. Positive results were seen with the increase in amount of AMPS, since, the total membrane resistance has been decreased from 0.95 (MR0) to 0.74 (MR4). Separation of humic acid from aqueous medium was also performed with the best performing membrane (MR4, having the highest amount of AMPS). Separation efficiency of 100% and 94% were obtained using 10 mg/L and 50 mg/L of HA, respectively. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45290.     

Outstanding antifouling performance of poly(vinylidene fluoride) membranes: Novel amphiphilic brushlike copolymer blends and one-step surface zwitterionization

In this study, we endowed a poly(vinylidene fluoride) (PVDF) membrane with outstanding antifouling ability by blending the hierarchical amphiphilic brushlike copolymer [poly(hydroxyethyl methacrylate)-b-polydimethylsiloxane-b-poly(hydroxyethyl methacrylate)]-g-poly(N,N-dimethylamino-2-ethyl methacrylate) with different initial monomer/initiator feed ratios and performing a one-step surface zwitterionization of spontaneously segregated poly(N,N-dimethyl aminoethyl methacrylate) segments. Interestingly, nanoscale granular micelles were formed on the surface during zwitterionization because of the migration and self-assembly of the amphiphilic copolymer; this contributed to the membrane hydrophilicity and antifouling ability. During the filtration of the model foulant bovine serum albumin (BSA) aqueous solution, the BSA rejection ratio and flux recovery ratio increased remarkably to 94.8 and 100.0%, respectively. Moreover, the modified membranes also possessed stable and durable antifouling properties after three cycles of BSA filtration. Thus, this study provided a versatile method for constructing a PVDF ultrafiltration membrane that could achieve high permeability and good antifouling properties in efficient wastewater treatment. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47637.     

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.     

Poly(vinylidene fluoride)–polyacrylonitrile blend flat‐sheet membranes reinforced with carbon nanotubes for wastewater treatment

In this reported study, poly(vinylidene fluoride) (PVDF) and polyacrylonitrile (PAN) blend flat‐sheet membranes were prepared via a phase‐inversion method with various loadings of multiwalled carbon nanotubes. The effects of the carbon nanotubes (CNTs) on the performance and morphology of the PVDF–PAN composites were investigated via tests of the pure water flux and rejection of bovine serum albumin, scanning electron microscopy, atomic force microscopy, Fourier transform infrared spectroscopy, X‐ray diffraction, thermogravimetric analysis, and contact angle (CA) analysis. The experimental results demonstrate that the CNTs contributed to the improvement of the flux and hydrophilicity of the membranes. The maximum value of the flux was 398.1 L m^?2 h^?1, and the value of CA for the composite membranes was found to be 48°. In addition, the results of the mechanical properties tests illustrate that the brittleness and plasticity of the hybrid membranes were greatly improved by the presence of the CNTs. The flux recovery ratio was maintained at 75%; this demonstrated that the PVDF–PAN membranes enhanced with the CNTs possessed good antifouling performance. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46155.