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The ceramic membrane has been widely used in the wastewater treatment based on the chemical resistance and superior separation performance. A robust and defect-free thin-film nanocomposite (TFN) nanofiltration (NF) membrane on the macroporous hollow fiber ceramic (HFC) substrate was novelly developed for heavy metals removal. Before interfacial polymerization (IP), the aqueous solution of graphene oxide (GO) grafted with ethylenediamine (EDA) was deposited on the HFC substrate by vacuum filtration. Then, a thin polyamide (PA) film was fabricated by EDA and 1,3,5-trimesoyl chloride (TMC), followed by heat treatment. The effects of GO content and EDA concentration on the performance of the NF membrane have been systematically investigated. The results showed that when the GO content was 0.015 mg·mL-1 and the EDA concentration was 0.75 wt.%, the as-prepared eGO3/PA-HFC membrane had a rejection rate of 94.12% for MgCl2 and a pure water flux of 18.03 L·m-2·h-1. Additionally, the removal ability of eGO3/PA-HFC membranes for heavy metal ions was satisfactory (93.33%, 92.73%, 90.45% and 88.35% for Zn2+, Cu2+, Ni2+ and Pb2+, respectively). The study explored further that it was efficient and stable for heavy metal ions removal during 30 h in the simulated tap water and mining wastewater, which indicated that the eGO/PA-HFC membrane has great application potential in wastewater treatment.
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Grafite , Metais Pesados , Nanocompostos , CerâmicaRESUMO
Graphene oxide (GO) membranes have great potential for separation applications due to their low-friction water permeation combined with unique molecular sieving ability. However, the practical use of deposited GO membranes is limited by the inferior mechanical robustness of the membrane composite structure derived from conventional deposition methods. Here, we report a nanostructured GO membrane that possesses great permeability and mechanical robustness. This composite membrane consists of an ultrathin selective GO nanofilm (as low as 32 nm thick) and a postsynthesized macroporous support layer that exhibits excellent stability in water and under practical permeability testing. By utilizing thin-film lift off (T-FLO) to fabricate membranes with precise optimizations in both selective and support layers, unprecedented water permeability (47 L·m-2·hr-1·bar-1) and high retention (>98% of solutes with hydrated radii larger than 4.9 Å) were obtained.
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Novel polyvinylidene fluoride/TiO2/UiO-66-NH2 (PVDF/TiUN) membranes were produced by the delay phase separation method via introducing the TiO2/UiO-66-NH2 (TiUN) nanocomposite into PVDF casting solution. Interconnection of TiO2 and UiO-66-NH2 improved photocatalysis capacity and endowed PVDF/TiUN membranes with self-cleaning capability. Quantitative measurements showed that, firstly, PVDF/TiUN membranes exhibited improved photodegradation kinetics and efficiency (up to 88.1%) to Rhodamine B (RhB). Secondly, the performances of bovine serum albumin (BSA) rejection and permeation of PVDF/TiUN membranes outperformed those of other check samples, indicating enhanced hydrophilicity. Thirdly, rejection rate of BSA reached a breathtaking 98.14% and flux recovery ratio (FRR) of BSA reached a breathtaking 95.37%. Thus, given their excellent anti-contamination property and separation performance, the PVDF/TiUN membrane is very likely to be a novel water treatment membrane.
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Incrustação Biológica , Estruturas Metalorgânicas , Incrustação Biológica/prevenção & controle , Membranas Artificiais , Polivinil , Titânio , ZircônioRESUMO
Fe3O4/Polyvinylidene fluoride (PVDF) three-channel hollow fiber catalytic membrane was successfully fabricated via non-solvent induced phase inversion and used for organic wastewater degradation in this work. The effects of Fe3O4 nanoparticles addition on the surface and cross-section morphologies, hydrophilicity and thermal properties of the catalytic membrane were characterized by the field emission scanning electron microscopy (SEM), water contact angle and thermogravimetric analysis (TGA), respectively. The obtained catalytic membrane exhibited good hydrophilicity, a high pure water flux of 175.8 L m-2 h-1 and a high removal of methylene blue (up to 97.6%) with Fenton catalytic reaction. Meanwhile, the catalytic membrane shows excellent anti-fouling property due to the presence of Fenton reaction. Our results show that Fe3O4/PVDF three-channel hollow fiber catalytic membrane was a promising alternative for the degradation of organic contaminants.
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Membranas Artificiais , Águas Residuárias , Permeabilidade , PolivinilRESUMO
In the past few decades, organic solvent nanofiltration (OSN) has attracted numerous researchers and broadly applied in various fields. Unlike conventional nanofiltration, OSN always faced a broad spectrum of solvents including polar solvents and non-polar solvents. Among those recently developed OSN membranes in lab-scale or widely used commercial membranes, researchers preferred to explore intrinsic materials or introduce nanomaterials into membranes to fabricate OSN membranes. However, the hydrophilicity of the membrane surface towards filtration performance was often ignored, which was the key factor in conventional aqueous nanofiltration. The influence of surface hydrophilicity on OSN performance was not studied systematically and thoroughly. Generally speaking, the hydrophilic OSN membranes performed well in the polar solvents while the hydrophobic OSN membranes work well in the non-polar solvent. Many review papers reviewed the basics, problems of the membranes, up-to-date studies, and applications at various levels. In this review, we have focused on the relationship between the surface hydrophilicity of OSN membranes and OSN performances. The history, theory, and mechanism of the OSN process were first recapped, followed by summarizing representative OSN research classified by surface hydrophilicity and types of membrane, which recent OSN research with its contact angles and filtration performance were listed. Finally, from the industrialization perspective, the application progress of hydrophilic and hydrophobic OSN membranes was introduced. We started with history and theory, presented many research and application cases of hydrophilic and hydrophobic OSN membranes, and discussed anticipated progress in the OSN field. Also, we pointed out some future research directions on the hydrophilicity of OSN membranes to deeply develop the effect made by membrane hydrophilicity on OSN performance for future considerations and stepping forward of the OSN industry.
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A novel pulluanase@chitosan porous beads/Poly (m-phthaloyl-m-phenylenediamine) (PULL@CPB/PMIA) membrane with good separation and biocatalysis properties was prepared by a self-adhesive method by introducing an immobilized enzyme (PULL@CPB) onto the PMIA membrane. The combination of PULL@CPB and PMIA could increase the one-step refining of protoplasmic beer as well as the ability of biocatalysis to lower the alcohol-to-ester ratio. The experimental results showed that the addition of PULL@CPB and the increase in the ratio of EtOH/water in the coagulation bath both increased the load of pullulanase on the membrane surface, while excessive addition decreased the activity of pullulanase. Under the amount of PULL@CPB is 0.5 g·L-1 and the ratio of EtOH/water is 60%, the relative activity of pullulanase in PULL@CPB modified PMIA membrane was the highest, which was 91.7% of the initial activity. The interception rates of protein and macromolecular ß-glucan were 92.2% and 87.3%, respectively, under the condition of beer flux (162.3 L·m-2·h-1). At the same time, the PULL@CPB/PMIA membrane has strong antibacterial performance and thus plays a role in extending the shelf life of beer. Compared with free pullulanase, the thermal stability, pH stability, organic solvent stability, and storing stability of immobilized pullulanase were significantly improved. The effects of PULL@CPB dosage and operating temperature on biocatalysis efficiency were discussed. The immobilized pullulanase activity on the membrane remained at 70.8% after 10 continuous uses. Therefore, the PMIA membrane is an excellent carrier of pullulanase, so its bioactive membrane has a wide range of prospects in food, medicine, and other fields.
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Quitosana , beta-Glucanas , Adesivos , Antibacterianos , Cerveja , Quitosana/química , Estabilidade Enzimática , Enzimas Imobilizadas/química , Ésteres , Glicosídeo Hidrolases , Concentração de Íons de Hidrogênio , Porosidade , Cimentos de Resina , Solventes , Temperatura , ÁguaRESUMO
Heavy metal ions in drinking water severely threaten public health in various places worldwide. Nanofiltration (NF) membrane technology is an attractive option for heavy metal ions removal; however, improving NF membrane filtration performance is required to make their industrial application viable. In this study, a positively charged THPC/PEI-TMC NF membrane was designed via simple one-step incorporation of Tetrakis (hydroxymethyl) phosphonium chloride (THPC) biocide on the surface of PEI-TMC membranes, significantly optimizing surface morphology, roughness, hydrophilicity, and zeta potential of PEI-TMC membranes. It was found that the pure water permeability (11.6 Lm-2h-1bar-1) of the THPC modified membrane was three times larger than that of the original PEI-TMC membrane (3.4 Lm-2h-1bar-1) while maintaining a high level of ion rejections (around 95% for Zn2+, Cd2+, Ni2+, Cu2+ and about 90% for Pb2+). Additionally, the incorporation of the THPC on the original PEI-TMC membrane surface also conferred good antibacterial properties, which protect the organic membrane from bacterial growth and prolong the lifespan of the membrane.
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Líquidos Iônicos , Metais Pesados , Antibacterianos/farmacologia , Íons , Membranas Artificiais , PermeabilidadeRESUMO
Objective: This study aims to explore the risk signals of osteonecrosis of the jaw induced by antiresorptive drugs and provide references for the clinical safety application. Method: According to the FDA's Adverse Event Reporting System (FAERS), from January 2004 to September 2021, we chose "Osteonecrosis of the jaw (10064658)" and "Exposed bone in jaw (10071014)" as preferred terms, "antiresorptive drugs" as the target drugs, and primary suspect drug as the drug role code in the dataset. We evaluated the association between drugs and adverse events by using reporting odds ratio (ROR) based on disproportionality analysis. We took the High-Level Terms (HLT) of MedDRA® as the classification level of indications to calculate ROR to compare the signal difference of ONJ in different indications. In addition, patients with antiresorptive-induced osteonecrosis of the jaw and the time of onset of the condition following different antiresorptive medications were collected for the study. Results: The FAERS contained 18,421 reports relating to jaw osteonecrosis from January 2004 to September 2021. A total of eight antiresorptive agents were included in the analysis. From high to low, the ROR of ONJ induced by antiresorptive agents (regardless of indication) is pamidronate (ROR = 494.8), zoledronic acid (ROR = 431.9), denosumab (ROR = 194.8), alendronate (ROR = 151.2), risedronate (ROR = 140.2), etidronic acid (ROR = 64.5), ibandronate (ROR = 40.8), and romosozumab (ROR = 6.4). HLT ROR values for "metabolic bone disorders" were the lowest for each drug, while HLT ROR values were high for "tumor-related indications," including breast and nipple neoplasms malignant, plasma cell myelomas, and prostatic neoplasms malignant. The onset time for osteonecrosis of the jaw as median (Q1, Q3), osteoporosis-related indications, and the onset time for ONJ were 730 (368, 1268), 489.5 (236.3, 909.8), 722.5 (314, 1055), 761 (368, 1720), and 153 (50, 346) for zoledronic acid, denosumab, ibandronate, risedronate, and romosozumab, respectively. Cancer-related indications: the onset time for ONJ were 680.5 (255.3, 1283), 488 (245, 851), and 696.5 (347, 1087) for zoledronic acid, denosumab, and pamidronate, respectively. Conclusion: When antiresorptive drugs are used for metastasis, they have the largest risk signal, followed by malignancy, and the smallest is osteoporosis. The onset time of ONJ may not be related to the indications. The onset time of ONJ for BPs was about 2 years, denosumab about 1.3 years, and romosozumab less than 1 year, which may be related to sequential treatment. When used according to the instructions, the risk of ONJ caused by denosumab was higher than that of zoledronic acid, regardless of the indication. Based on these findings, researchers will continue to monitor and identify risk factors.
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Catalytic membrane plays an important role in environmental remedy. In this study, we reported an Ag coated membrane (PAN-Si-Cu-Ag) with a high catalytic activity to reduce 4-nitrophenol (4-NP) and methyl orange (MO) from water. The best performance is 99% reduction degree and 280 L m-2.h-1.bar-1 flux for (4-NP) reduction at 4-NP: NaBH4 = 1:50 (mM) during a 12-h filtration. The reduction degree for MO is above 90% and the flux is about 230 L m-2·h-1·bar-1, which is almost the best report till now. The Ag coated membrane was prepared by metal displacement-epitaxial growth on silica covalent grafted PAN membrane (PAN-Si). Silica atoms were used as linker to ensure the good adhesion between polymer and metal NPs, the loss amount of Ag NPs from the coated catalytic membrane is loss about 2 µg/cm2 after one month storage. Cheap metal NPs were firstly reduced on the surface of PAN-Si membrane and then used to displace Ag ions. Thus the obtained catalytic membrane showed a very high loading (28%). Finally, the catalytic filtration mechanism of 4-NP was distinguished by Cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and adsorption measurement.
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Nanopartículas Metálicas , Prata , Catálise , NitrofenóisRESUMO
Thin-film composite (TFC) membranes are attracting wide attention because their ultrathin selective layer usually corresponds to the higher membrane flux for pervaporation. However, the direct preparation of the TFC membranes on ceramic substrates confronted with the great difficulties because the larger pores on ceramic substrate surfaces are detrimental to the formation of an intact polyamide (PA) selective layer produced by interfacial polymerization (IP) reaction. Here, the integrated ZIF-L nanosheets were proposed to be used as an assistance interlayer for the first time to eliminate the existence of the pores of the ceramic support, and provides a better basis for the formation of an intact PA selective layer by IP reaction between TMC and ethylenediamine (EDA). The experimental data obtained in pervaporation (PV) show that the increased flux from 1.1 to 2.9 kg/m2h corresponds to the decreased separation factor from 396 to 110 when the feed concentration of ethanol decreases from 95 wt % to 80 wt % at 50 °C. In addition, the membrane flux increases from 0.8 to 2.5 kg/m2h with a change of the separation factor from 683 to 111 when the operational temperature varies from 30 to 60 °C. These results demonstrate the great potential of the fabricated TFC membranes in practical application for PV dehydration of organic solutions.
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A homologous series of hyperbranched polyesters (HBPEs) was successfully synthesized via an esterification reaction of 2,2-bis(methylol)propionic acid (bis-MPA) with pentaerythritol. The molecular weights of the HBPEs were 2160, 2660, 4150 and 5840 g/mol, respectively. These HBPEs were used as additives to prepare polysulfone (PSf) hollow fiber membranes via non-solvent induced phase separation. The characteristic behaviors of the casting solution were investigated, as well as the morphologies, hydrophilicity and mechanical properties of the PSf membranes. The results showed that the initial viscosities of the casting solutions were increased, and the shear-thinning phenomenon became increasingly obvious. The demixing rate first increased and then decreased when increasing the HBPE molecular weight, and the turning point was 2660 g/mol. The PSf hollow fiber membranes with different molecular weights of HBPEs had a co-existing morphology of double finger-like and sponge-like structures. The starting pure water contact angle decreased obviously, and the mechanical properties improved.
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The dye-water treatment using UF membrane is still a challenge. In the present study, the optimized PAN-ETA ultrafiltration membrane was hydrolyzed and subsequently characterized by SEM, IR, CA, XPS, NMR, mechanic measurement, etc. The obtained membrane (H-PAN-ETA) was used for dye removal and it showed both an excellent anti-dye fouling and a good rejection property for anionic dyes. I.e. 96% rejection for methyl blue (MB), 99% for congo red (CR), 94% for acid fuchsin (AF) with no sign of contamination by dye. The flux of H-PAN-ETA membrane maintained at 50-53 L m-2â h-1 during a 10-h filtration, which is higher than that of tight UF membranes reported. Meanwhile, H-PAN-ETA membrane was able to selectively remove cationic dyes, such as methylene blue (MEB), rhodamine B (RB) and, crystal violet (CV), or the mixture of anionic dye/cationic dye by adsorption process. Its adsorption capacity remained unchanged after 20 cycles. Finally, the immobile electrical double layer (EDL) theory combined with electrostatic force was introduced to explain the separation mechanism of charged UF membrane, which is helpful to instruct the preparation of UF membrane for dye removal.
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Resinas Acrílicas/química , Corantes/química , Etanolamina/química , Purificação da Água/métodos , Adsorção , Ânions , Cátions , Filtração , Membranas , Membranas Artificiais , Azul de Metileno , Rodaminas , UltrafiltraçãoRESUMO
The thin-film composite (TFC) nanofiltration (NF) membrane is a very important method in solving the water crisis. However, the fabrication and industrialization of high-performance NF membranes still remains challenging. In this work, zwitterionic NF membranes via microwave-assisted grafting of betaine was first proposed. The resulting polyamide layer showed leaflike nanostructures after modification. Because of the enlarged permeation area and enhanced hydrophilicity derived from the unique leaflike structure, the optimal membrane permeability reached 40.8 L m-1 h-1 bar-1. This water permeance was 2.2 times as high as the original polypiperazine-amide membrane, with a Na2SO4 rejection maintained at 97.0%. More importantly, the membrane demonstrated excellent selectivity to monovalent and divalent anions. This zwitterionic membrane fabricated by microwave-assisted grafting of betaine provides new insight for industrial scalable NF membranes with great potentials.
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Designing nanocatalysts with synergetic functional component is a desirable strategy to achieve both high activity and selectivity for industrially important hydrogenation reaction. Herein, we fabricated a core-shell hollow Au@Pt NTs@ZIFs (ZIF, zeolitic imidazolate framework; NT, nanotube) nanocomposite as highly efficient catalysts for semi-hydrogenation of acetylene. Hollow Au@Pt NTs were synthesized by epitaxial growth of Pt shell on Au nanorods followed with oxidative etching of Au@Pt nanorod. The obtained hollow Au@Pt NTs were then homogeneously encapsulated within ZIFs through in situ crystallization. By combining the high activity of bimetallic nanotube and gas enrichment property of porous metal-organic frameworks, hollow Au@Pt NT@ZIF catalyst was demonstrated to show superior catalytic performance for the semi-hydrogenation of acetylene, in terms of both selectivity and activity, over those of monometallic Au and solid bimetal nanorod@ZIF counterparts. This catalysts design idea is believed to be inspirable for the development of highly efficient nanocomposite catalysts.
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Membrane fouling in the membrane bioreactor (MBR) is typically caused by the interaction of microbial characteristics, hydrodynamic behavior, operation environment, wastewater characteristics and membrane properties, which result in the deterioration of performance and increasing energy consumption and cost of membrane replacement. The effect of the crucial MBR parameters (the microbial loading and characteristics, dissolved oxygen (DO), hydraulic retention time (HRT), backwashing conditions and membrane characteristics) on membrane fouling was investigated in a submerged membrane bioreactor (SMBR) during the long term treatment of synthetic coke wastewater. Also the optimum operation strategies were further utilized in order to satisfy the minimal membrane fouling operation through a long-term evaluation of the MBR performance. It has been demonstrated that with application of these optimal designed conditions, significant membrane fouling improvements were achieved over a long operating time, so it was possible to perform in sustainable operation for MBR. In this study, the upper limit of the sustainable flux is found to be as much as 18.6 L/m(2) h and the optimum sustainable flux value should be 50 approximately 75% of critical flux to satisfy the desired sustainable operation period.
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Reatores Biológicos , Coque/análise , Conservação dos Recursos Naturais/métodos , Membranas Artificiais , Eliminação de Resíduos Líquidos/métodos , Purificação da Água/métodos , Incrustação Biológica , Reatores Biológicos/microbiologia , Espaço Extracelular/metabolismo , Filtração , Oxigênio/metabolismo , Polímeros/metabolismo , Polivinil , Pressão , Fatores de TempoRESUMO
Sulfonated polyethersulfone (SPES) was used as an additive to prepare hydrophilic poly(ethersulfone) (PES) hollow fiber membranes via non-solvent assisted reverse thermally induced phase separation (RTIPS) process. The PES/SPES/N,N-dimethylacetamide (DMAc)/ polyethylene glycol 200 (PEG200) casting solutions are lower critical solution temperature (LCST) membrane forming systems. The LCST and phase separation rate increased with the increase of SPES concentrations, while the casting solutions showed shear thinning. When the membrane forming temperature was higher than the LCST, membrane formation mechanism was controlled by non-solvent assisted RTIPS process and the also membranes presented a more porous structure on the surface and a bi-continuous structure on the cross section. The membranes prepared by applying SPES present higher pure water flux than that of the pure PES membrane. The advantages of the SPES additive are reflected by the relatively high flux, good hydrophilicity and excellent mechanical properties at 0.5 wt.% SPES content.
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Graphene oxide (GO), as a two-dimensional structure material, has attracted widespread attention in the field of molecule sieving. However, GO-based membranes usually exhibit undesirable separation performance because the microstructure of GO is difficult to adjust. Herein, a novel double-crosslinking strategy for tuning the interlayer spacing of GO is reported. The hybrid membrane fabricated by the double-crosslinking strategy was used for pervaporation (PV) dehydration of isopropanol. To achieve high-performance of the PV hybrid membranes, the effects of operating cycles, chitosan concentration, and GO concentration were systematically investigated. The PV hybrid membranes were characterized by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, water contact angle measurement, and scanning electron microscopy. The results demonstrate that the interlayer of GO can be adjusted successfully by the double-crosslinking strategy. The fabricated hybrid membrane containing 0.1 wt % GO exhibited excellent performance with a flux of 4391 g/m2h and a separation factor of 1491, which indicated that the double-crosslinking strategy may extend the applications of GO in the field of membrane separation.
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Nanofiltration (NF) membranes with simultaneous high rejection of divalent cations and anions and high water permeation were designed and fabricated via interfacial polymerization (IP) on three-channel capillary ultrafiltration (UF) membranes. MWCNTs-COOH were modified with poly(amidoamine) (PAMAM) and the as-synthesized MWCNTs-PAMAM were embedded into the inner polyamide skin-layer of the NF membranes by incorporating them into a piperazine (PIP) aqueous solution, followed by IP with trimesoyl chloride (TMC). The rigid MWCNTs and the dendrimer PAMAM molecules endow the as-fabricated NF membranes with high porosity and good hydrophilicity. Additionally, the -NH2 groups of PAMAM introduce some positive sites into the polyamide layer. The as-prepared NF membranes with incorporated MWCNTs-PAMAM exhibit a pure water flux of 48.7 L m-2 h-1 and 92.6% and 88.5% rejection for Na2SO4 and MgCl2, respectively, at 4 bar. Moreover, the NF membranes display high rejection for sulfates and metal cations, including heavy metal ions. The practicability of the membranes for mine-wastewater treatment was tested, and the membranes showed above 80% rejection of heavy metals and solution flux of about 30 L m-2 h-1. In addition, their separation performance and stability were satisfactory during the long-term run. The high rejection of the membranes for metal cations is ascribed to the positive sites offered by MWCNTs-PAMAM and the narrow membrane pores since both electrostatic repulsion and size exclusion play a role during membrane filtration. The good separation performance of the membranes for multivalent anions and heavy metal cations illustrates their potential for applications in heavy metal wastewater treatment.
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Polyacrylonitrile (PAN) is a popular material in membrane field because of its excellent mechanical property, thermal stability, and chemical resistance. Unfortunately, PAN nanofibers produced by electrospinning are not suitable for interfacial polymerization process directly due to its hydrophobicity and large average pore size. In this work, the cross-linked chitosan (CS) solution was coated on the nanofiber surface to fabricate a sublayer, based on which thin-film composite (TFC) membranes were prepared using m-phenylenediamine and 1,3,5-trimesoyl chloride as the monomers. The impact of the different sublayers on the performances of TFC PAN nanofiber membranes for forward osmosis (FO) was studied by varying cross-linked CS concentrations. The results indicated that the increased CS concentration not only led to the relatively denser polyamide layer, but also changed its morphology. In the reverse osmosis process, NaCl rejection increased from 46.5 to 83.5%. Salt flux from feed solution to draw solution decreased from 25.8 to 8.9 g·m-2·h-1 (0.1 M NaCl solution as feed, 2 M glucose solution as draw solution, FO mode). This study found that the sublayer had noteworthy impact on the separation layer and helped us to pave the way to design high-performance FO membranes.
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A novel antifouling polyethersulfone (PES) hollow fiber membrane was modified by the addition of bisphenol sulfuric acid (BPA-PS) using a reverse thermally induced phase separation (RTIPS) process. BPA-PS was synthesized by click chemistry and was blended to improve the hydrophilicity of PES hollow fiber membranes. The performance of PES/BPA-PS hollow fiber membranes, prepared with different contents of BPA-PS and at different temperatures of the coagulation water bath, was characterized by scanning electron microscopy (SEM), pure water flux (J w), BSA rejection rate (R), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and water contact angle measurements. SEM morphologies revealed that a finger-like cross-section emerged in the hollow fiber membrane by a non-solvent induced phase separation (NIPS) mechanism while a sponge-like cross-section appeared in the hollow fiber membrane via the RTIPS method. Both FTIR and XPS analysis indicated that the sulfate group in BPA-PS was successfully blended with the PES membranes. The results from AFM and water contact angle measurements showed that the surface roughness increased and the hydrophilicity of the PES/BPA-PS hollow fiber membrane was improved with the addition of BPA-PS. The results demonstrated that the PES/BPA-PS membrane with 1 wt% BPA-PS via RTIPS exhibited optimal properties.