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ACS Applied Materials & Interfaces · 2021 · IF 9.229

Smart Self-Cleaning Membrane via the Blending of an Upper Critical Solution Temperature Diblock Copolymer with PVDF

Xinying Jia,Hailan Ji,Ganwei Zhang,Jiale Xing,Shusu Shen,Xiaoji Zhou,Suling Sun,Xu Wu,Danfeng Yu,Ian Wyman

Poly(2,2,2-trifluoroethyl methacrylate)-b-poly(imidazoled glycidyl methacrylate-co-diethylene glycol methyl ether methacrylate) (PTFEMA-b-P(iGMA-co-MEO2MA)) containing an upper critical solution temperature (UCST) polymer chain was prepared and blended with poly(vinylidene fluoride) (PVDF) to produce a thermoresponsive membrane with smart self-cleaning performance. The successful preparation of the membrane was demonstrated by attenuated total reflection–Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy characterization. The membrane shows UCST performance, and its flux changes with the filtrate temperature as the UCST polymer chain stretches out and contracts in response to various temperatures. In addition, the UCST polymer chain can disrupt the foulant and push it away from the membrane when the temperature is above the UCST and thus enables membranes to exhibit a smart self-cleaning behavior. To the best of our knowledge, this work is the first report of a smart self-cleaning membrane based on the blending of a diblock copolymer containing a UCST polymer chain with PVDF.

研究领域: 材料科学 · 膜技术 · 高分子化学 · 环境工程
✓ 已验证 DOI 高影响因子
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ACS Sustainable Chemistry & Engineering · 2019 · IF 6.97

Solvent-Free Crystallization of Zeolitic Imidazolate Framework Membrane via Layer-by-Layer Deposition

Pingping Yang,Zhan Li,Zhuangzhuang Gao,Mingqiu Song,Jinya Zhou,Qianrong Fang,Ming Xue,Shilun Qiu

Searching for sustainable synthesis methods of metal–organic framework (MOF) membranes has received huge attention in both academia and industry. In this contribution, the compact ZIF-8 membrane with excellent gas separation performance was successfully prepared via an environmentally friendly and simple method, in which the artful layer-by-layer deposition approach was used to achieve the solvent-free crystallization of a well-intergrown and defect-free ZIF-8 membrane. The solvent-free process is a simple and generalized method for construction of MOF membranes, which can avoid using solvents and high autogenous pressure and brings great benefits for energy saving, emission reduction, and safety as well as scalable manufacturing. In addition, the solvent-free crystallization of MOF membranes exhibits more unprecedented advantages to fill the common intercrystalline cracks, pinhole defects, and grain boundary defects on the membrane. The resulting thin ZIF-8 membrane exhibited both competitive H2 permeability of 6.7 × 10–7 mol m–2 s–1 Pa–1 and high H2/CO2 selectivity of 12.3, simultaneously, which is one of the best ZIF-8 membranes ever reported.

研究领域: 材料科学 · 膜技术 · 可持续化学 · 分离科学
✓ 已验证 DOI 高影响因子
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JOURNAL OF MEMBRANE SCIENCE · 2015 · IF 5.056

Enhancing the hydrophilicity and water permeability of polypropylene membranes by nitric acid activation and metal oxide deposition

He Chen,Liang Kong,Yong Wang

Activation by nitric acid oxidation has been combined with atomic layer deposition (ALD) to modify microporous polypropylene (PP) membranes. Nitric acid oxidation with prewetting of t -butanol generates active groups on the inert surface of PP membranes. Metal oxides including Al 2 O 3 and TiO 2 are subsequently ALD-deposited on the activated membrane. Nitric acid oxidation is a mild approach to activate PP membranes. A short immersion in nitric acid for 10   min is able to generate oxygen/nitrogen-containing active species on the membrane surface , which leads to an evident increase (38%) in the membrane permeability. The mechanical stability and the integrity of the porous structure are well preserved after activation. Surface elemental analyses and microscopy observations confirm the successful deposition of metal oxides thin layers onto the activated membranes. In the deposition of either Al 2 O 3 or TiO 2 , the hydrophilicity of the deposited membranes is continuously improved with increasing ALD cycles, resulting in further increase in water flux. After 100 ALD cycles, the flux is doubled compared to that of the bare membrane. Al 2 O 3 is more efficient in enhancing the hydrophilicity and permeation than TiO 2 under identical deposition conditions because of the faster growth of Al 2 O 3 on the activated PP surface.

研究领域: 材料科学 · 膜技术 · 表面化学 · 高分子化学 · 化学工程
✓ 已验证 DOI 高影响因子
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JOURNAL OF MEMBRANE SCIENCE · 2016 · IF 5.557

A catechol-based biomimetic strategy combined with surface mineralization to enhance hydrophilicity and anti-fouling property of PTFE flat membrane

Sikuai Xue,Chengcai Li,Jiuming Li,Hailin Zhu,Yuhai Guo

To improve hydrophilicity and anti-fouling property of the polytetrafluoroethylene (PTFE) flat microfiltration (MF) membrane, a facile method was developed to modify the membrane via the co-deposition of catechol (CA) and polyethyleneimine (PEI) followed by surface mineralization of γ-(2,3-epoxypropoxy) propytrimethoxysilane (KH560). The surface chemical composition, surface morphology, hydrophilicity and filtration performance of the PTFE flat membrane were investigated by ATR-FTIR, XPS, FESEM, WCA and pure water flux measurements, respectively. After using this low-cost and simple modification method, the PTFE flat membrane was endowed with excellent hydrophilicity, high water permeation flux and superior anti-fouling property. Then, the oil/water separation tests were conducted using the modified PTFE flat membranes. The size distribution of the oil droplets is between 0.12–1.44   µm and the mean pore size of pristine PTFE flat MF membrane is 0.22   µm. The as-prepared hydrophilized PTFE flat membranes possess an excellent oil resistant ability with oil rejection ratio near 99%. Finally, the surface stability of the modified membrane was studied and the mineralized membrane showed excellent acid resistant ability. Therefore, this facile strategy holds attractive potential practical application in water environmental remediation.

研究领域: 材料科学 · 环境工程 · 膜技术 · 表面化学 · 水处理
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Desalination and Water Treatment · 2024 · IF 1

Preparation and characterization of a high flux nanofiltration polyamide hollow fiber TFC membrane for drinking water production

Wan Su,Yufeng Zhang,Wenjuan Zhang,Shuting Xie,Xiaobo Sun,Jianqiang Meng

In this study, a nanofiltration (NF) polyamide hollow fiber thin film composite membrane with a low rejection and a high flux was prepared in consideration of the “trade-off” relation between salt rejection and permeate flux of the membrane. The membrane was able to retain the beneficial minerals in tap water while keeping the body healthy. The membrane prepared had a thinner active skin layer (<100 nm) than those of commercial membranes. A permeability of 30.07 L/m 2 /h and a rejection rate of 79.68% for 1,000 mg/L MgSO 4 at 0.2 MPa were obtained. In addiiton, Fe 3+ , Cu 2+ , and Pb 2+ were used to evaluate the heavy metal removal performance of the NF membrane. It was found that as the concentration of heavy metal ions increased to three times of the Standards for Drinking Water Quality (SDWQ) (GB5749-2006), and the rejections to all heavy metal ions were more than 76%. In addition, the NF membrane had a good long-term rejection stability for the heavy metal ions over a 12-month dynamic filtration experiment. The results showed that the newly prepared NF membrane has a good application prospect for domestic water purification.

研究领域: 环境科学 · 材料科学 · 膜技术 · 水处理 · 纳米技术 · 化学工程 · 公共卫生工程
✓ 已验证 DOI 高影响因子
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Journal of Zhejiang University-SCIENCE A · 2017 ·Vol. 18 ·期 2 ·138-150 · IF 1.214

Fabrication of composite nanofiltration membranes by dopamine-assisted poly(ethylene imine) deposition and cross-linking

Zhang Pei-bin,Liu Cui-jing,Sun Jian,Zhu Bao-ku,Zhu Li-ping

Positively charged composite nanofiltration (NF) membranes with good stability were prepared by dopamine (DA) assisted poly(ethylene imine) (PEI) deposition on a polysulfone ultrafiltration (UF) substrate followed by a cross-linking step. Attenuated total reflectance Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electronic microscopy, and atom force microscopy were employed to characterize the surface chemistry and morphology of the obtained composite membranes. The DA and PEI co-deposition conditions were optimized based on knowledge of the co-deposition mechanism. The effects of the cross-linker concentration, cross-linking time, and reaction temperature on the permeation and separation properties of the prepared composite membranes were investigated in detail. Under optimized conditions, the MgCl 2 rejection and permeation flux of the composite membrane reached 80.4% and 19.6 L/(m 2 ·h), respectively (the feed was 0.01 mol/L of MgCl 2 solution under a test pressure of 0.4 MPa). The rejection of various salts followed the order MgCl 2 ≈CaCl 2 >MgSO 4 >NaCl>Na 2 SO 4 , suggesting the membranes were positively charged. The composite membranes showed good durability under alkaline aqueous conditions. This study provided new insights into the fabrication of mussel-inspired thin-film composite nanofiltration membranes.

研究领域: 材料科学 · 膜技术 · 环境工程 · 分离科学
✓ 已验证 DOI 高影响因子
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JOURNAL OF MEMBRANE SCIENCE · 2019 · IF 7.015

Double network anion exchange membrane with excellent flexibility and stability

Xinming Du,Zhe Wang,Hongyu Zhang,Wenchang Liu,Zhaoyu Chen,Jingmei Xu

A double-network anion exchange membrane (TA/AT-PEK/PVA-x) was prepared by Br-PEK and PVA , 3-amino-1,2,4 triazole forms a cross-linking structure with PVA under the action of 1,4-phthalaldehyde and then triazole can be linked with Br-PEK. The structure of membranes was verified by FT-IR. The composite membrane is uniform and smooth can be seen from the scanning electron microscope (SEM) and exhibit good hydrophilic/hydrophobic micro-phase separation structure proved by Transmission electron micrograph (TEM). The ionic conductivity of TA/AT-PEK/PVA-0.15 is 0.062 S/cm at 80 °C. With the addition of PVA within a certain range, the water uptake, swelling ratio hydroxide conductivity and alkaline stability are increase. The membranes are more flexible. After immersing in 4 M NaOH solutions for 240 h at 80 °C, it remains at least 65% of its initial hydroxide ion conductivity of TA/AT-PEK/PVA-0.3 membrane. With the increasing number of water molecules solvating the hydroxide, its nucleophilicity and basicity were hindered, which enhance alkaline stability of anion exchange membranes.

研究领域: 材料科学 · 高分子化学 · 能源材料 · 膜技术 · 电化学
✓ 已验证 DOI 高影响因子
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MATERIALS CHEMISTRY AND PHYSICS · 2021 · IF 4.094

Effect of the molecular weight of polymer and diluent on the performance of hydrophilic poly(vinyl butyral) porous heddle via thermally induced phase separation

Yunying Luo,Fan Yang,Chengcai Li,Feng Wang,Hailin Zhu,Yuhai Guo

Hydrophilic Poly (vinyl butyral) (PVB) porous heddles were prepared via blending hydrophilic PVB and green diluent Polyethylene glycol (PEG) through liquid-liquid thermally induced phase separation (TIPS) process. To further investigate the effect of the molecular weight (MW) of polymer and diluent on phase diagram of PVB-PEG blending system and performance of hydrophilic PVB porous heddle, the cloud point (Tcloud), microstructure, overall porosity and mechanical property, i.e were mainly analyzed. The results highlighted that the Tcloud of the PVB-PEG blending shifted to lower temperature with increasing PEG MW and PVB MW. Overall porosity reached up to 82.3% and tensile strength was 9.88 MPa when polymer and diluent with lowest MW. To extend the application air, the fabrication conditions of prepared porous heddle were studied. Overall porosity increased and the tensile strength decreased with extrusion temperature increasing. In addition, the PVB-PEG porous heddles proved effective hydrophilic performance and demonstrate the potential application in water treatment.

研究领域: 高分子科学 · 材料工程 · 膜技术 · 相分离 · 水处理
✓ 已验证 DOI 高影响因子
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POLYMER · 2020 · IF 4.231

High conductivity and alkali-resistant stability of imidazole side chain crosslinked anion exchange membrane

Kai Yang,Hongzhe Ni,Tianen Shui,Xiaoyu Chi,Wenbo Chen,Qian Liu,Jingmei Xu,Zhe Wang

Poly (aryl ether ketone) polymers (PAEKS) were synthesized by polycondensation of trimethyl hydroquinone , allyl bisphenol S and 4,4-difluorodiphenyl ketone as monomers . A series of uncrosslinked and crosslinked anion exchange membranes (AEMs) with diverse contents of 1-allyl-3-methylimidazolium chloride and 1-vinylimidazole were prepared by grafting and bromination reaction. The 1-vinylimidazole in the AEMs was simultaneously present as a crosslinked agent. 1 HNMR and FT-IR spectra demonstrated the structure of the above PAEKS and AEMs, respectively. TEM images and SAXS profiles showed the formation of distinct hydrophilic/hydrophobic microphase separation in the TCImP membranes, which offered vast of channels for ion transmission. Among them, TCImP-3 membrane showed the highest hydroxide conductivity of 0.144 S/cm at 80 °C. Compared with the uncrosslinked AEMs, the crosslinked AEMs exhibited slightly lower water uptake and swelling ratio. The crosslinked structures in the AEMs were helpful to improve the mechanical property and alkali-resistant stability of AEMs. The hydroxide conductivity of the TCImP-3 membrane kept 0.117 S/cm in 2 M NaOH solutions at 80 °C for 400 h. Meanwhile, crosslinked AEMs showed excellent thermostability. We believe that TCImP membranes are a promising AEMs material.

研究领域: 材料科学 · 高分子化学 · 能源材料 · 膜技术 · 电化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF MEMBRANE SCIENCE · 2018 · IF 6.578

Long-side-chain type imidazolium-functionalized fluoro-methyl poly(arylene ether ketone) anion exchange membranes with superior electrodialysis performance

Junbin Liao,Jiajie Zhu,Shanshan Yang,Nengxiu Pan,Xinyan Yu,Chao Wang,Jun Li,Jiangnan Shen

Developing highly ion conductive and desirable electrodialysis (ED) performance anion exchange membranes (AEMs) is of great significance. In this work, we report a strategy for fabricating novel AEMs based on a series of fluoro-methyl poly(arylene ether ketone)s having long-side-chain imidazolium groups for ED. Having hydrophilic conductive flexible side-chain imidazolium groups and rigid hydrophobic backbone within AEM matrix, the optimized AEM (PAEK-60-im) shows low water uptake of 24.9% at 80 °C and desirable ion conductivity of 22.01 mS cm –1 at 30 °C. In NaCl removal application of ED, PAEK-60-im shows the NaCl removal ratio of 69.66% within 120 min, outperforming commercial AEM-Type II (68.98%). Accordingly, it has a higher current efficiency of 83.7% but lower energy consumption of 5.9 kWh kg –1 , compared with the commercial one (82.0%; 6.6 kWh kg –1 ). In particular, in selectrodialysis application, possibly owing to the synergistic effect of pore-size sieving effect resulting from macro-separation morphology and hydration energy difference of SO 4 2– ions (–1000 kJ mol –1 ) and Cl – ions (–317 kJ mol –1 ) in feeding solution, PAEK-60-im shows significantly superior monovalent anion perm-selectivity (Cl − /SO 4 2− ) of 7.70 at 30 min, relative to commercial anion-selective Neosepta ACS (5.27) and many other reported mono-valent anion selective AEMs having elegant surface modified layers. The superior ED performance of the homogeneous PAEK-60-im is suggestive of its potential separation application.

研究领域: 材料科学 · 化学工程 · 电化学 · 膜技术
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