Publications by authors named "Quanfu An"

Aromaticaliphatic hydrocarbon separation is a challenging but important industrial process. Pervaporation membrane technology has the potential for separating these mixtures. We developed an oriented monolayer polyhedral (OMP) membrane that consists of a monolayer of ordered polyhedral particles and is anchored by hyperbranched polymers.

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Recycling of valuable solutes and recovery of organic solvents via organic solvent nanofiltration (OSN) are important for sustainable development. However, the trade-off between solvent permeability and solute rejection hampers the application of OSN membranes. To address this issue, the poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) nanoparticle membrane with hierarchical pores is constructed for OSN via vacuum filtration.

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Article Synopsis
  • * The membranes are made from specially engineered fibers that combine a strong core for durability with a responsive outer layer that can change properties based on CO levels.
  • * These membranes not only achieve over 99.6% separation efficiency but also offer self-cleaning capabilities and can be produced in large sizes, making them suitable for practical industrial applications.
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Organic solvent nanofiltration (OSN) plays important roles in pharmaceutical ingredients purification and solvent recovery. However, the low organic solvent permeance under cross-flow operation of OSN membrane hampers their industrial applications. Herein, we report the construction of coffee-ring structured membrane featuring high OSN permeance.

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Conductive polymers are recognized as ideal candidates for the development of noninvasive and wearable sensors for real-time monitoring of potassium ions (K) in sweat to ensure the health of life. However, the low ion-to-electron transduction efficiency and limited active surface area hamper the development of high-performance sensors for low-concentration K detection in the sweat. Herein, a wearable K sensor is developed by tailoring the nanostructure of polypyrrole (PPy), serving as an ion-to-electron transduction layer, for accurately and stably tracing the K fluctuation in human sweat.

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Mixed-matrix membranes (MMMs) have the potential for energy-efficient gas separation by matching the superior mass transfer and anti-plasticization properties of the fillers with processability and scaling up features of the polymers. However, construction of high-performance MMMs has been prohibited due to low filler-loading and the existence of interfacial defects. Here, high MOF-loaded, i.

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Two-dimensional (2D) membrane-based ion separation technology has been increasingly explored to address the problem of lithium resource shortage, yet it remains a sound challenge to design 2D membranes of high selectivity and permeability for ion separation applications. Zeolitic imidazolate framework functionalized modified layered double hydroxide (ZIF-8@MLDH) composite membranes with high lithium-ion (Li) permeability and excellent operational stability were obtained in this work by in situ depositing functional ZIF-8 nanoparticles into the nanopores acting as framework defects in MLDH membranes. The defect-rich framework amplified the permeability of Li, and the site-selective growth of ZIF-8 in the framework defects bettered its selectivity.

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The successful implementation of thin-film composite membranes (TFCM) for challenging solute-solute separations in the pharmaceutical industry requires a fine control over the microstructure (size, distribution, and connectivity of the free-volume elements) and thickness of the selective layer. For example, desalinating antibiotic streams requires highly interconnected free-volume elements of the right size to block antibiotics but allow the passage of salt ions and water. Here, we introduce stevioside, a plant-derived contorted glycoside, as a promising aqueous phase monomer for optimizing the microstructure of TFCM made via interfacial polymerization.

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With the increasing demands for novel flexible organic electronic devices, conductive polymers are now becoming the rising star for reaching such targets, which has witnessed significant breakthroughs in the fields of thermoelectric devices, solar cells, sensors, and hydrogels during the past decade due to their outstanding conductivity, solution-processing ability, as well as tailorability. However, the commercialization of those devices still lags markedly behind the corresponding research advances, arising from the not high enough performance and limited manufacturing techniques. The conductivity and micro/nano-structure of conductive polymer films are two critical factors for achieving high-performance microdevices.

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Azeotropic organic solvent mixture separation is common in the chemical industry but extremely difficult. Zeolitic imidazolate framework-67 (ZIF-67) shows great potential in organic solvent mixture separation due to its rigid micropores and excellent stability. However, due to the fast nucleation rate, it is a great challenge to prepare continuous ZIF-67 membrane layers with ultrathin thickness.

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Mixed matrix membranes (MMMs), conjugating the advantages of flexible processing-ability of polymers and high-speed mass transfer of porous fillers, are recognized as the next-generation high-performance CO capture membranes for solving the current global climate challenge. However, controlling the crystallization of porous metal-organic frameworks (MOFs) and thus the close stacking of MOF nanocrystals in the confined polymer matrix is still undoable, which thus cannot fully utilize the superior transport attribute of MOF channels. In this study, the "confined swelling coupled solvent-controlled crystallization" strategy is employed for well-tailoring the in-situ crystallization of MOF nanocrystals, realizing rapid (<5 min) construction of defect-free freeway channels for CO transportation in MMMs due to the close stacking of MOF nanocrystals.

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The pursuit of improved water purification technology has motivated extensive research on novel membrane materials to be carried out. In this paper, one-dimensional carboxylated carbon nanotubes (CNTs) were intercalated into the interlayer space of layered double hydroxide (LDH) to form a composite membrane for water purification. The CNTs/LDH laminates were deposited on the surface of the hydrolyzed polyacrylonitrile (PAN) ultrafiltration membrane through a vacuum-assisted assembly strategy.

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Article Synopsis
  • Polymeric nanomaterials are gaining attention for creating high-performance separation membranes due to their adjustable properties and compatibility with existing polymers, which can help resolve issues like permeability-selectivity trade-offs and fouling.
  • Recent research focuses on enhancing the design and surface qualities of these membranes through various fabrication techniques, such as phase inversion and self-assembly, to elevate their effectiveness.
  • The review covers membrane fabrication methods, strategies for modifying surface and microstructural properties, and details about their performance in separating liquid and gas molecules, alongside highlighting ongoing challenges and opportunities in advancing these materials.
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Functional membranes generally wear out when applying in harsh conditions such as a strong acidic environment. In this work, high acid-resistance, long-lasting, and low-cost functional membranes are prepared from engineered hydrogen-bonding and pH-responsive supramolecular nanoparticle materials. As a proof of concept, the prepared membranes for dehydration of alcohols are utilized.

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Nanofluidics derived from low-dimensional nanosheets and protein nanochannels are crucial for advanced catalysis, sensing, and separation. However, polymer nanofluidics is halted by complicated preparation and miniaturized sizes. This work reports the bottom-up synthesis of modular nanofluidics by confined growth of ultrathin metal-organic frameworks (MOFs) in a polymer membrane consisting of zwitterionic dopamine nanoparticles (ZNPs).

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Assembling two-dimensional (2D) materials by polyelectrolyte often suffers from inhomogeneous microstructures due to the conventional mixing-and-simultaneous-complexation procedure ("mix-and-complex") in aqueous solution. Herein a "mix-then-on-demand-complex" concept on-demand cascade anionization and ionic complexation of 2D materials is raised that drastically improves structural order in 2D assemblies, as exemplified by classical graphene oxide (GO)-based ultrathin membranes. Specifically, in dimethyl sulfoxide, the carboxylic acid-functionalized GO sheets (COOH-GOs) were mixed evenly with a cationic poly(ionic liquid) (PIL) and upon filtration formed a well-ordered layered composite membrane with homogeneous distribution of PIL chains in it; next, whenever needed, it was alkali-treated to convert COOH-GO into its anionized state COO-GO that immediately complexed ionically with the surrounding cationic PIL chains.

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The robustness of carbon nanomaterials and their potential for ultrahigh permeability has drawn substantial interest for separation processes. However, graphene oxide membranes (GOms) have demonstrated limited viability due to instabilities in their microstructure that lead to failure under cross-flow conditions and applied hydraulic pressure. Here we present a highly stable and ultrapermeable zeolitic imidazolate framework-8 (ZIF-8)-nanocrystal-hybridized GOm that is prepared by ice templating and subsequent in situ crystallization of ZIF-8 at the nanosheet edges.

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Water transport rate in network membranes is inversely correlated to thickness, thus superior permeance is achievable with ultrathin membranes prepared by complicated methods circumventing nanofilm weakness and defects. Conferring ultrahigh permeance to easily prepared thicker membranes remains challenging. Here, a tetrakis(hydroxymethyl) phosphonium chloride (THPC) monomer is discovered that enables straightforward modification of polyamide composite membranes.

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Article Synopsis
  • * Researchers are focusing on membranes that incorporate "ion pairs," which enhance properties like super-hydrophilicity, controllable charge characteristics, and antifouling capabilities.
  • * This review covers the methods for creating various types of membranes (polyelectrolyte complex, zwitterionic, and charged mosaic), examines their performance in mass transport and antifouling, and suggests future advancements in membrane technology.
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Article Synopsis
  • Membrane performance in thin-film composite nanofiltration is significantly influenced by the properties of the polysulfone (PSf) supports, which were modified by adding polyethylene glycol (PEG) of different molecular weights.
  • A process called interfacial polymerization led to the formation of a thin polyamide layer on the PSf surface, with the presence of PEG confirmed through advanced imaging techniques.
  • The resulting membrane, specifically TFC-PEG20k, showed outstanding water flux and separation efficiency due to its low porosity and favorable hydrophilicity, making it effective in rejecting negatively charged dyes.
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  • A thermoresponsive chitosan derivative was created by modifying chitosan with butyl glycidyl ether, allowing it to respond to temperature changes by undergoing a phase transition.
  • The modification resulted in a lower critical solution temperature (LCST) compared to regular chitosan, with varying BGE content influencing the LCST and particle behavior under different temperatures.
  • The derivative showed promising properties such as nontoxicity (92% cell survival) and effective performance in forward osmosis tests, indicating potential applications in dehydration processes.
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  • * Researchers developed high-flux nanofiltration membranes by incorporating these modified carbon nanotubes into polyamide thin-film composites, resulting in improved water permeability.
  • * The optimized membrane exhibited a pure water permeability rate of 15.32 L m(-2) h(-1) bar(-1), which is significantly higher than traditional membranes, while also showing effective salt rejection for various multivalent cations, making it useful for water softening and heavy metal ion removal.
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Hydrophilic polymers have garnered much attention due to their critical roles in various applications such as molecular separation membranes, bio-interfaces, and surface engineering. However, a long-standing problem is that their mechanical properties usually deteriorate at high relative humidity (RH). Through the simultaneous incorporation of functionalized carbon nanotubes and copper ions (Cu(2+)), this study introduces a facile method to fabricate high strength polyelectrolyte complex nanohybrid membranes resistant to high RH (90%).

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Carboxymethyl cellulose (CMC)-modified silica nanocomposites were prepared via in situ incorporation of modified silica during the ionic complexation between CMC and poly(2-methacryloyloxy ethyl trimethylammonium chloride) (PDMC). Ionic bonds were introduced between the poly(2-acrylamido-2-methylproanesulfonic acid) modified silica (SiO2-PAMPS) and the polyelectrolyte complex (PEC) matrix. The PEC nanocomposites (PECNs) and their membranes (PECNMs) were characterized with Fourier transform-infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and tensile testing.

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A technique of layer-by-layer (LbL) self-assembly was used to prepare transparent multilayered gas barrier films consisting of graphene oxide (GO)/branched poly(ethylenimine) (BPEI) on a poly(ethylene terephthalate) substrate. The effect of the GO suspension pH on the nanostructure and oxygen barrier properties of the GO/BPEI film was investigated. The oxygen barrier properties of the assemblies were shown to be highly dependent on the pH.

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