Yong-Ming Wei

FAS Grafted Electrospun Poly(vinyl alcohol) Nanofiber Membranes with Robust Superhydrophobicity for Membrane Distillation

This study develops a novel type of electrospun nanofiber membranes (ENMs) with high permeability and robust superhydrophobicity for membrane distillation (MD) process by mimicking the unique unitary microstructures of ramee leaves. The superhydrophobic ENMs were fabricated by the eletrospinning of poly(vinyl alcohol) (PVA), followed by chemical cross-linking with glutaraldehyde and surface modification via low surface energy fluoroalkylsilane (FAS). The resultant FAS grafted PVA (F-PVA) nanofiber membranes were endowed with self-cleaning properties with water contact angles of 158° and sliding angles of 4° via the modification process, while retaining their high porosities and interconnected open structures. For the first time, the robust superhydrophobicity of the ENMs for MD was confirmed by testing the F-PVA nanofiber membranes under violent ultrasonic treatment and harsh chemical conditions. Furthermore, vacuum membrane distillation experiments illustrated that the F-PVA membranes presented a high and stable permeate flux of 25.2 kg/m2 h, 70% higher than those of the commercial PTFE membranes, with satisfied permeate conductivity (<5 μm/cm) during a continuous test of 16 h (3.5 wt % NaCl as the feed solution, and feed temperature and permeate pressure were set as 333 K and 9 kPa, respectively), suggesting their great potentials in myriad MD processes such as high salinity water desalination and volatile organiccompounds removal.

Processing–Structure–Property Correlations of Polyethersulfone/Perfluorosulfonic Acid Nanofibers Fabricated via Electrospinning from Polymer–Nanoparticle Suspensions

Polyethersulfone (PES)/perfluorosulfonic acid (PFSA) nanofiber membranes were successfully fabricated via electrospinning method from polymer solutions containing dispersed calcium carbonate (CaCO(3)) nanoparticles. ATR-FTIR spectra indicated that the nanoparticles mainly existed on the external surface of the nanofibers and could be removed completely by acid treatment. Surface roughness of both the nanofibers and the nanofiber membranes increased with the CaCO(3) loading. Although FTIR spectra showed no special interaction between sulfonic acid (-SO(3)) groups and CaCO(3) nanoparticles, XPS measurement demonstrated that the content of -SO(3) groups on external surface of the acid-treated nanofibers was enhanced by increasing CaCO(3) loading in solution. Besides, the acid-treated nanofiber membranes were performed in esterification reactions, and exhibited acceptable catalytic performance due to the activity of -SO(3)H groups on the nanofiber surface. More importantly, this type of membrane was very easy to separate and recover, which made it a potential substitution for traditional liquid acid catalysts.

Novel polyamide thin-film composite nanofiltration membrane modified with poly(amidoamine) and SiO2 gel

Recently, poly(amidoamine) (PAMAM) has emerged as a novel material due to its high density of functional groups, hyper-branched structure and hydrophilic nature. PAMAM has been used as a monomer during an interfacial polymerization process for the fabrication of nanofiltration membranes. Previous work has focused on the low generation of PAMAM (G0, G1 and G2), however, the high generation of PAMAM (G4 and G5) still lacks investigation. This work focuses on the preparation of nanofiltration membranes, which are made of PAMAM–NH2 G4 and PAMAM–NH2 G5. By optimizing the concentration of PIP and SiO2 gel in the aqueous solution, the pure water flux improved by 106% while separation properties are kept at the same level. XPS, EDS, SEM, AFM and contact angle were used to characterize the NF membrane properties. The PAMAM/PIP/SiO2 membrane prepared under the optimum conditions exhibited a pure water flux of 38.5 L m−2 h−1 and Na2SO4 rejection of 92.0% under 0.6 MPa. The PAMAM/PIP/SiO2 membrane’s robust long-time running performance showed its good potential in practical applications.

Formation of microporous polymeric membranes via thermally induced phase separation: A review

A review of recent research related to microporous polymeric membranes formed via thermally induced phase separation (TIPS) and the morphologies of these membranes is presented. A summary of polymers and suitable diluents that can be used to prepare these microporous membranes via TIPS are summarized. The effects of different kinds of polymer materials, diluent types, cooling conditions, extractants and additive agents on the morphology and performance of TIPS membranes are also discussed. Finally new developments in TIPS technology are summarized.

Preparation of porous PVDF nanofiber coated with Ag NPs for photocatalysis application

The porous Polyvinylidene fluoride (PVDF) nanofibers were prepared by leaching method using polyethylene oxide (PEO) as porogen for the first time. The influences of the molecular weight (MW) and concentration of PEO, and the leaching solution on the morphology and the surface area of the porous PVDF nanofiber were systematically investigated. Polyethylene glycol 6000 (PEG6000) showed a better pore-forming effect. Optimized preparation parameters were obtained. With the ratio of PEG6000/PVDF reaching 1:1, the surface area of the resulting porous PVDF nanofiber was about three times higher than that of the pure PVDF nanofiber. Moreover, NaClO solution as leaching solution showed a very limited influence on the surface area of porous PVDF nanofiber. Afterwards, Ag NPs coated PVDF (Ag/PVDF) nanofiber was prepared by physical adsorption of Ag ions and in-situ reduction reaction using sodium borohydride as reductant. The photoactivity of Ag/PVDF nanofiber was evaluated by the photodegradation of methyl orange (MO) under visible light irradiation. Ag/PVDF nanofiber showed a better photoactivity than PVDF-Ag nanofiber prepared by the ex-situ blending method.

Preparation of PAN/PAMAM blend nanofiber mats as efficient adsorbent for dye removal

PAN/PAMAM blend nanofiber mats with different ratios were prepared by electrospinning process for the first time. Their structures were characterized by SEM, N2 adsorption/desorption and contact angle. It was found that PAN/PAMAM nanofiber with ratio of 12:3 has the highest surface area. The adsorption of methyl orange on blend nanofiber was investigated. With the ratio of PAMAM increasing in blend nanofiber, the adsorption capacity increased not very much. Overall the PAN/PAMAM nanofiber with ratio of 12:3 has the best property, its maximum adsorption capacity was found to be 120 mg/g although its surface area was only about 9.97 m2/g. It still maintained an efficient adsorption capacity even at 5th experiment, indicating an effective adsorbent for dye removal. The adsorption isotherm and adsorption kinetics were further investigated. The Freundlich isotherm provided the best fit for dye adsorption and the dynamical data fitted well with the second-order kinetic model. The possible mechanism was discussed.

A polyethersulfone–bisphenol sulfuric acid hollow fiber ultrafiltration membrane fabricated by a reverse thermally induced phase separation process

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 (Jw), 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.