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JOURNAL OF MATERIALS RESEARCH · 2021 ·Vol. 36 ·期 4 ·925-937 · IF 3.089

A novel polysaccharide-grafted gold nanoparticles synthesized via carboxyl-trithiocarbonates for modification of separation membrane

Zhang Shaohu,Niu Xiaoqin,Wang Qi,Li Dan,Zhang Weijie,Chen Yuhong,Ran Fen

Abstract Permeability and selectivity are two important parameters for evaluating membrane separation performance. In this work, the polysaccharide-functionalized gold nanoparticles (DexDTM-AuNP) are synthesized by one-step reduction with NaBH 4 and used as additive for modification of PES membrane to improve the hydrophilicity of the membrane. In comparison with the pristine PES membrane, the water contact angle (WCA) of the DexDTM-AuNP-modified membrane significantly decreases. When the content of DexDTM-AuNP is 3 wt%, the WCA of the modified membrane decreases from 89.3° to 61.1°, indicating excellent hydrophilicity. The modified membrane shows high pure water flux of up to 134.5 L m −2  h −1 , and the rejection ratio for bovine serum albumin, congo red, and methyl blue are 98.8, 99.3, and 93.6%, respectively. DexDTM-AuNP-modified membrane exhibits excellent hydrophilicity, anti-fouling ability, and separation performance. Therefore, the strategy has great potential for practical applications in water purification and other separation fields. Graphic Abstract

研究领域: 材料科学 · 环境工程 · 生物技术
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CHEMOSPHERE · 2023 · IF 8.8

Structural and performance variation of PES/PVDF membranes after exposure to the pretreated feed water of CECs

Jun Young Kim,Kang Hoon Lee,Jae Won Lee,Imtiaz Afzal Khan,Jong-Oh Kim

In this study, the removal efficiency of chemicals of emerging concerns (CECs) was evaluated under exposure to various doses of UV/H 2 O 2 -based oxidation processes in combination with membrane filtration for three cleaning cycles. Polyethersulphone (PES) and polyvinylidene fluoride (PVDF) materials based membranes were used for this study. The chemical cleaning of the membranes was performed by immersion of the membranes into 1 N HCl followed by adding 3000 mg.L −1 NaOCl for 1hr. Degradation and filtration performance was evaluated using Liquid Chromatography with tandem mass spectrometry (LC-MS/MS) and total organic carbon (TOC) analysis. Membrane fouling analysis for assessing the comparative performance of PES and PVDF membranes was determined by specific fouling and fouling indices evaluation. Membrane characterization results show that the alkynes and carbonyl group formation are due to dehydrofluorination and oxidation of PVDF and PES membranes under the attack of foulants and cleaning chemicals, which resulted in a reduction of fluoride percentage and an increase in sulfur percentage in the PVDF and PES membranes. A decrease in the hydrophilicity of the membranes in underexposed conditions was observed and is consistent with an increase in dose. Degradation results of CECs follow with the highest removal efficiency of chlortetracycline (CTC) followed by atenolol (ATL), acetaminophen (ACT), and caffeine (CAF) degradation due to attack on the aromatic ring and the carbonyl group of CECs by OH exposure. Membrane exposed at 3 mg.L-1 dose of UV/H 2 O 2 -based CECs shows minimum alteration with higher filtration efficiency and lower fouling, particularly in PES membranes.

CAS / MDL: 29122-68-7
研究领域: 环境科学 · 材料科学
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Journal of Hazardous Materials Advances · 2022 · IF 0

Inhibition of membrane biofouling by grafting quorum sensing inhibitors onto ultrafiltration membranes

Rukang Tian,Xiaofang Ma,Yan Wang,Hong Mei,Yunkun Wang

Quorum sensing inhibitors (QSIs) can inhibit biofilm formation by regulating the synthesis of extracellular polymeric substances (EPS), thus alleviating biofouling in the membrane filtration process. In this study, utilizing the adhesion ability of a mussel-inspired biomimetic material, polydopamine (PDA), natural quorum sensing inhibitors, vanillin and furanone, were modified on a commercial polyethersulfone (PES) ultrafiltration (UF) membrane to inhibit the formation of biofilm fouling. We proved that QSIs were successfully grafted onto the membrane surface without blocking the pore structure, and the pure water flux of the membrane was simultaneously improved due to hydrophilicity improvement. The vanillin-modified membrane significantly inhibited the biofilm formation of P. aeruginosa PAO1 (81.7% inhibition rate), while furanone had a certain inhibitory effect on E. coli MG1655 and PAO1. We also tested the modified membrane in the dynamic filtration of simulated wastewater, in which both modified membranes alleviated biofouling.

研究领域: 环境科学 · 微生物学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2020 · IF 7.489

Magnetic field assisted arrangement of photocatalytic TiO2 particles on membrane surface to enhance membrane antifouling performance for water treatment

Tianyu Sun,Ying Liu,Liguo Shen,Yanchao Xu,Renjie Li,Lilin Huang,Hongjun Lin

Fabrication of membranes with high antifouling and self-cleaning ability is a long-term pursuit of research community. For this purpose, the current work proposed a strategy to use an external magnetic field to arrange the magnetic TiO 2 @Ni particles (MNPs) onto the polymeric polyether sulfone (PES) membrane surface. The characterization results clearly indicated that the MNPs were successfully embedded onto the membrane surface instead of uniformly distributing into the membrane bulk. Because of this superficial distribution, the prepared composite membrane exhibited a flux of 871.2 ± 2.9 L·m −2 ·h −1 ·bar −1 , which was 5 times flux of the pristine PES membrane. Meanwhile, it remained a rejection of 95.85% bovine serum albumin (BSA), which was also better than that of the pristine PES membrane. The cycle filtration experiments verified that the composite membrane possessed promoted antifouling ability for filtrating BSA, yeast extract fermentation (YEF), ammonium alginate (SA) and humic acid (HA) solutions. The antifouling mechanism was analyzed by the total interaction energies (ΔG Total ), which were quantitatively evaluated by using the extended Derjaguin–Landau–Verwey–Overbeek (XDLVO) theory. Moreover, it was interestingly found that the composite membrane possessed a self-cleaning property under radiation of UV light and sunlight. The optimal membrane after self-cleaning presented flux recovery ratio (FRR) of 75.4%, 99.56%, 92.11% and 98.26% for BSA, YEF, SA and HA solutions, respectively. This work demonstrated a novel way to fabricate membranes with high antifouling and self-cleaning ability for water treatment.

CAS / MDL: 13463-67-7 51-61-6
研究领域: 环境工程 · 材料科学 · 水处理
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JOURNAL OF MEMBRANE SCIENCE · 2020 · IF 7.183

In situ metal-polyphenol interfacial assembly tailored superwetting PES/SPES/MPN membranes for oil-in-water emulsion separation

Ruoxi Wang,Xueting Zhao,Youyou Lan,Lifen Liu,Congjie Gao

Superhydrophilic and underwater superoleophobic membranes have recently attracted increased attention in oily wastewater treatment because of their potential to promote membrane permeability and minimize membrane fouling . Despite recent advances, the manipulation of membrane superwettability is usually achieved by coating functional layers on commercial hydrophobic porous substrates. The direct fabrication of superhydrophilic and underwater superoleophobic microporous membranes still remains a challenge. In this work, we provide a new in situ metal-polyphenol interfacial assembly strategy and prepare a new type of superwetting PES/SPES/MPN membranes. In the phase inversion of membrane formation, the coordination assembly of tannic acid (TA) and transition metal ions takes place alone with the solvent/nonsolvent exchange, resulting in the in situ deposition of metal-polyphenol networks (MPNs) on as-prepared polyether sulfone (PES)/sulfonated polyether sulfone (SPES) membranes. The PES/SPES/MPN membranes exhibit hierarchical surfaces and bi-continuous pores, and the in situ deposited MPNs provide hydrophilic bases. Among them, the PES/SPES/TA-Fe 3+ membrane showed the highest superhydrophilicity and underwater superoleophobicity. Thanks to the excellent superhydrophilicity, the water flux of PES/SPES/TA-Fe 3+ membrane can reach 4423 Lm −2 h −1 . Moreover, the PES/SPES/TA-Fe 3+ membrane exhibits high-performance for oil-in-water emulsion separation with high flux (>1500 Lm −2 h −1 ), excellent oil rejection (>99.5%) and reliable enhanced antifouling and recycling performance. This study provides a novel and facile strategy for the direct fabrication of superwetting microporous membranes, and predicts the potential application of PES/SPES/MPN membranes in oily wastewater treatment.

研究领域: 材料科学 · 环境工程
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Journal of Environmental Chemical Engineering · 2022 · IF 7.968

Construction of PES membranes using NH2-MIL-125 and Pluronic F127 via RTIPS method toward elevated ultrafiltration, antifouling and self-cleaning performance

Jinchao Chen,Chunmei Gao,Shuangquan Zhao,Shenghui Liu,Shifeng Ji,Yunqing Xing,Tianyang Wu,Jinjian Wu,Hongyu Chen,Peng Zou,Jiaonan Cai

In this work, the NH 2 -MIL-125/F127/PES membranes with superior ultrafiltration , anti-fouling and self-cleaning were constructed via the RTIPS method. Characterizations showed the successful fabrication of NH 2 -MIL-125 with good photocatalysis activities, together with its stable anchoring in PES membrane. The loss of NH 2 -MIL-125 was suppressed by hydrogen bond between F127 and NH 2 -MIL-125, where hydrophilic F127 significantly boosted permeability and anti-fouling property. The permeability-selectivity trade-off effect was alleviated by NH 2 -MIL-125 with a regular size window. It was observed that the membranes prepared by the RTIPS method occurred a spongy-like cross-section and a porous surface, which imparted the membrane with improved ultrafiltration and mechanical properties over the finger-like cross-section and dense skin caused by the NIPS method. The optimal membranes exhibited decent permeability (1511 L/m 2 h), BSA rejection rate (85.3%) and high COD removal rate over the commercial membranes, whose flux recovery rate was up to 76.91% after two cycles under light irradiation by the synergistic effect of F127 and NH 2 -MIL-125. The membrane fouled with RhB exhibited excellent regeneration properties benefiting from the holes (h + ) and superoxide free radicals ( • O 2 − •O2− ), as well as reactive •OH. Overall, the membrane with F127 and NH 2 -MIL-125 presented a highly promising in improving ultrafiltration and self-cleaning via the RTIPS method.

CAS / MDL: 67-56-1 5593-70-4
研究领域: 材料科学 · 环境工程 · 化学工程 · 纳米技术
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Polymer Chemistry · 2014 ·Vol. 5 ·期 11 ·3563-3575 · IF 5.368

Self-assembled 3D biocompatible and bioactive layer at the macro-interface via graphene-based supermolecules

Hongju Zhou,Chong Cheng,Hui Qin,Lang Ma,Chao He,Shengqiang Nie,Xiang Zhang,Qiang Fu,Changsheng Zhao

Research on the interface self-assembly of functional layers is fuelled by diverse biomedical needs, like drug encapsulation and release, stem cell proliferation and differentiation, cell and tissue cultures, as well as artificial organs. In this study, a novel and biocompatible 3D composite layer is fabricated on a membrane substrate by the layer-by-layer (LBL) self-assembly of graphene-based 2D supermolecules. The graphene-based 2D supermolecules are prepared by grafting poly(styrenesulfonate) (PSS, polyanion) and poly(acrylamide) (PAM, polycation) onto graphene oxide (GO) through free radical polymerization. Then, the prepared graphene-based supermolecules are taken to construct a 3D porous thin film layer through a LBL process. Polyethersulfone (PES) membrane is chosen as the model substrate. The chemical composition, surface morphology, water contact angle, surface zeta-potential, blood compatibility and the cell compatibility are systematically investigated. The results indicate that the 2D graphene-based supermolecules are successfully assembled into a 3D porous thin film layer structure on the membrane surface. The assembled layer shows increased hydrophilicity, suppressed platelet adhesion, and a limited hemolysis ratio and complement activation compared to the pristine substrate. The cell morphology observation and cytotoxicity assays demonstrate that the 3D graphene layer shows superior performance both in endothelial and hepatocyte cells proliferation and morphology differentiation. In addition, the excellent anticoagulant bioactivities indicate that the 2D graphene-based supermolecules have heparin-mimicking biological activity. In general, the protocol of interface thin film layer self-assembly confers the modified substrates with integrated blood compatibility, cell proliferation and biological activity; which may forward the fabrication of multi-functional biomedical devices by using the 2D graphene-based supermolecules.

研究领域: 生物医学工程 · 材料科学 · 生物材料 · 组织工程
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POLYMER · 2011 · IF 3.829

A readily modified polyethersulfone with amino-substituted groups: Its amphiphilic copolymer synthesis and membrane application

Zhuan Yi,Liping Zhu,Liang Cheng,Baoku Zhu,Youyi Xu

An amino-substituted polyethersulfone (PES) was synthesized by the polycondensation of a functional monomer bis(3-amino-4-hydroxyphenyl) sulfone with bis(4-fluorophenyl) sulfone. The amine groups incorporated into PES were employed as anchors to immobilize the chain transfer agents of reversible addition-fragmentation polymerization (RAFT). The resultant macro chain transfer agent was used to initiate the polymerization of the hydrophilic monomers N -isopropyl acrylamino (NIPAAm) and N, N -dimethylamino-2-ethyl methacrylate (DMAEMA), respectively. The gel permeation chromatography (GPC) results confirmed the successful synthesis of the amphiphilic copolymers PES- g -PNIPAAm and PES- g -PDMAEMA, and these two copolymers were perhaps the few examples of amphiphilic copolymer synthesized via a radical polymerization from PES main chains. The amino-substituted PES seemed a versatile precursor that showed a potential of functionalization via various strategies including click chemistry, atom transfer radical polymerization and RAFT polymerization. The synthesized amphiphilic copolymers were finally used as additives to improve the hydrophilicity and the filtration performances of PES membranes.

CAS / MDL: 5407-87-4 538-75-0
研究领域: 高分子化学 · 材料科学 · 膜技术
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