Track-etched Membranes Research Articles

Liquid gated membrane with self-cleaning properties for controllable removal and multi-component separation of organic/bacterial contaminants

Membrane technology plays an important role in sustainable water treatment; however, the non-adjustable pores make it difficult to achieve precise molecular separation, and membrane fouling remains a challenge in membrane processes. Herein, a smart liquid gated membrane (LGM) was prepared by filling different lubricants in the micropores of PET track-etched membrane that was pre-treated with nano roughening and fluorination. When the pressure exceeds a critical breakthrough pressure, the liquid lined pores are formed, and higher gating liquid/water interfacial tension requires higher pressure to break through the gate. The effective pore size of LGM increases with increasing pressure. When the pressure is removed, the liquid refilling that leads to pore-closing is promoted by lower lubricant viscosity and larger effective pore size. Through the tunable permeability, controllable removal and multi-component separation of organic/bacterial contaminants can be achieved. The maximum rejection for protein approaches 94 %; as the pressure increases, three components are separated in the order of pectin, soy protein isolate and Staphylococcus aureus with maximum separation coefficient of 56.7. Due to the stable lubricant lining, LGM shows excellent self-cleaning performance with much higher flux recovery rate than the non-lubricated membranes. This liquid gated membrane has great application prospects in size-fractionated separation and product recovery.

Ion transport across bilayer lipid membranes using a track-etched membrane filter

Bilayer lipid membranes (BLM) are widely employed to study the electrochemical behavior across cell membranes, particularly the ion transport in the presence of hydrophobic ions or ionophores. However, owing to the physical fragility of BLMs, they are readily broken down by external shocks, such as the applications of a potential difference, current, and vibration. Thus, in this study, a facile method for enhancing the physical stability of BLMs was developed using a track-etched membrane (TM). Physically stable BLMs were rapidly fabricated within the apertures of TM by dropping an n-decane solution containing lecithin and cholesterol on TM. Therefore, BLM formation was confirmed by capacitance measurement, and the estimated membrane thickness and mean capacitance were 3.5 ± 0.4 nm and 0.51 ± 0.05 μF cm−2, respectively. The applied membrane potential could be extended to ≥1.5 V, which is approximately 10 times higher than those of conventional BLMs, and the lifetime exceeded 40 min. The applicability of the fabricated BLM was verified by electrochemical measurements during ion transport.

Modification of Track-Etched Polyethylene Terephthalate Membranes with Functionalized Silanes for Immobilizing Silver Nanoparticles

Modification of Track-Etched Polyethylene Terephthalate Membranes with Functionalized Silanes for Immobilizing Silver Nanoparticles

Integration of 2D Nanoporous Membranes in Microfluidic Devices.

2D material-based membranes have emerged as promising candidates for next-generation separation technology due to their exceptional permeability and selectivity. Integration of these membranes into microfluidic devices has offered significant potential for improving the efficiency, throughput, and precision. However, designing compact and reliable microfluidic devices with membranes has many challenges, including complexities in membrane integration, analyte measurement, and contamination issues. Addressing these challenges is critical for unlocking the full potential of membrane-integrated devices. This paper proposes a systematic procedure for integrating membranes into a microfluidic device by creating a pore in the middle layer. Furthermore, an ion transport experiment is carried out across various stacked graphene and poly carbonate track etch membranes in an Ostemer-based device. The resulting device is capable of facilitating the concurrent measurement, a task that is cumbersome in standard macroscopic diffusion cells. The transparency and compactness of the microfluidic device allowed for the in situ and real-time optical characterization of analytes. The integration of microfluidic devices with 2D nanoporous membranes has enabled the incorporation of several analytical modalities, resulting in a highly versatile platform with numerous applications.

Isoporous Membrane Mediated Imprinting Mass Spectrometry Imaging for Spatially-Resolved Metabolomics and Rapid Histopathological Diagnosis.

Surface-assisted laser desorption/ionization (SALDI) mass spectrometry imaging (MSI) holds great value in spatial metabolomics and tumor diagnosis. Tissue imprinting on the SALDI target can avoid laser-induced tissue ablation and simplifies the sample preparation. However, the tissue imprinting process always causes lateral diffusion of biomolecules, thereby losing the fidelity of metabolite distribution on tissue. Herein, a membrane-mediated imprinting mass spectrometry imaging (MMI-MSI) strategy is proposed using isoporous nuclepore track-etched membrane as a mediating imprinting layer to selectively transport metabolites through uniform and vertical pores onto silicon nanowires (SiNWs) array. Compared with conventional direct imprinting technique, MMI-MSI can not only exclude the adsorption of large biomolecules but also avoid the lateral diffusion of metabolites. The whole time for MMI-based sample preparation can be reduced to 2min, and the lipid peak number can increase from 46 to 113 in kidney tissue detection. Meanwhile, higher resolution of MSI can be achieved due to the confinement effect of the pore channel in the diffusion of metabolites. Based on MMI-MSI, the tumor margins of liver cancer can be clearly discriminated and their different subtypes can be precisely classified. This work demonstrates MMI-MSI is a rapid, highly sensitive, robust and high-resolution technique for spatially-resolved metabolomics and pathological diagnosis.

Track-etched membrane as a thin substrate with straight pores to fabricate polyamide forward osmosis membrane

Controlling the internal concentration polarization in forward osmosis (FO) membranes by minimizing the substrate thickness is critical to enhancing the water flux. This study aimed to achieve the fabrication of an ultra-thin FO membrane by forming the polyamide (PA) active layer on a thin and straight-bore film, a so-called track-etched (TE) membrane. The polycarbonate TE membrane had a uniform pore size of 0.22 µm and a thickness of 25 µm. The PA active layer was successfully formed only by creating a thin m-phenylenediamine solution layer on the smooth TE membrane surface before interfacial polymerization. The TE- FO membrane with low porosity (14 %) provided a water flux of 21 L/m2h and a reverse salt flux of 8.0 g/m2h when evaluated with a 1.0 M NaCl draw solution. Further evaluations showed the potential of increasing water flux by increasing the TE substrate porosity (14 %) and reducing the apparent PA active layer thickness (504 nm). These results suggest the potential of achieving a high-water flux FO membrane using a thin TE substrate and ultimately improving the validity of FO membrane-based water treatment.

Fabrication of Breathable Multifunctional On-Skin Electronics Based on Tunable Track-Etched Membranes

Fabrication of Breathable Multifunctional On-Skin Electronics Based on Tunable Track-Etched Membranes

Structural Characterization and Physicochemical Properties of Functionally Porous Proton-Exchange Membrane Based on PVDF-SPA Graft Copolymers.

Fluorinated proton-exchange membranes (PEMs) based on graft copolymers of dehydrofluorinated polyvinylidene fluoride (D-PVDF), 3-sulfopropyl acrylate (SPA), and 1H, 1H, 2H-perfluoro-1-hexene (PFH) were prepared via free radical copolymerization and characterized for fuel cell application. The membrane morphology and physical properties were studied via small-(SAXS) and wide-angle X-ray scattering (WAXS), SEM, and DSC. It was found that the crystallinity degree is 17% for PEM-RCF (co-polymer with SPA) and 16% for PEM-RCF-2 (copolymer with SPA and PFH). The designed membranes possess crystallite grains of 5-6 nm in diameter. SEM images reveal a structure with open pores on the surface of diameters from 20 to 140 nm. Their transport and electrochemical characterization shows that the lowest membrane area resistance (0.9 Ωcm2) is comparable to perfluorosulfonic acid PEMs (such as Nafion®) and polyvinylidene fluoride (PVDF) based CJMC cation-exchange membranes (ChemJoy Polymer Materials, China). Key transport and physicochemical properties of new and commercial membranes were compared. The PEM-RCF permeability to NaCl diffusion is rather high, which is due to a relatively low concentration of fixed sulfonate groups. Voltammetry confers that the electrochemical behavior of new PEM correlates to that of commercial cation-exchange membranes, while the ionic conductivity reveals an impact of the extended pores, as in track-etched membranes.

Композиционные мембраны для обессоливания воды

Methods of coatings forming on the surface of a poly(ethylene terephthalate) track-etched membrane by magnetron and electron-beam sputter deposition of polytetrafluoroethylene in vacuum are considered. It is established that the involve of these modification methods leads to the formation of composite membranes consisting of two layers, one of which is the original track-etched membrane, characterized by an average level of hydrophilicity. The second layer has a hydrophobic nature. The contact angle of wettability by water of this layer varies depending on its thickness and the modification method used. It is shown that deposition of coatings by magnetron sputtering of polytetrafluoroethylene leads to smoothing of structural inhomogeneities of the surface of the initial membrane. Deposition of coatings by electron-beam dispersion of polymer, on the contrary, causes an increase in surface roughness. The observed differences in the morphology of the composite membranes surface layer are related to the size of the deposited polymer nanostructures. Nanostructures formed on the surface of track-etched membranes, when polytetrafluoroethylene is dispersed under the action of electron beam, have greatly large sizes. A significant increase in roughness due to the increase in the size of nanostructures makes it possible to obtain coatings with high- and superhydrophobic properties. It is shown that composite membranes consisting of a hydrophilic base with a hydrophobic coating deposited on the surface provide higher separation selectivity during desalination of an aqueous solution of sodium chloride by membrane distillation compared with the initial poly(ethylene terephthalate) track-etched membrane. In addition, the performance of two-layer composite membranes in the process of membrane distillation due to low resistance to mass transfer is higher in comparison with a track-etched membrane made of polypropylene.

Effect of hydrophobized PET TeMs membrane pore-size on saline water treatment by direct contact membrane distillation.

This paper describes the desalination process by membrane distillation (MD) using track-etched membranes (TeMs). Hydrophobic track-etched membranes based on poly(ethylene terephthalate) (PET TeMs) with pore diameters from 700 to 1300 nm were prepared by UV-initiated graft polymerization of lauryl methacrylate (LMA) inside the nanochannels. Modified PET TeMs were investigated by Fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), scanning electron microscopy (SEM), thermogravimetric analysis (TGA) and contact wetting angle (CA) measurements. Hydrophobic PET TeMs were tested for treating saline solutions of different concentrations by the direct contact membrane distillation (DCMD) method. The influence of membrane pore diameter and salt solution concentration on the water flux and rejection degree were investigated. Membranes with CA 94 ± 4° were tested in the direct contact membrane distillation (DCMD) of 7.5-30 g L-1 saline solution. Hydrophobic membranes with large pore sizes showed water fluxes in the range of 1.88 to 11.70 kg m-2 h-1 with salt rejection values of up to 91.4%.

Preparation and application of stimuli-responsive PET TeMs: RAFT graft block copolymerisation of styrene and acrylic acid for the separation of water-oil emulsions.

Stimuli-responsive membranes play an important role in the fields of biomedicine, food and chemical industries, and environmental applications, including separation of water-oil emulsions. In this study, we present a method to fabricate pH-sensitive membranes using UV-initiated RAFT graft copolymerization of styrene (ST) and acrylic acid (AA) on poly(ethylene terephthalate) (PET) track-etched membranes (TeMs). The optimization of polymerization conditions led to successful grafting of polystyrene (PS) and poly(acrylic acid) (PAA) onto PET TeMs, resulting in membranes with stable hydrophobicity and pH change responsiveness. The membranes show a contact angle of 65° in basic environments (pH 9) and 97° in acidic environments (pH 2). The membranes were characterized by atomic force microscopy (AFM), scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX), thermogravimetric analyses (TGA), Fourier transform infrared spectroscopy (FTIR), contact angle (CA) methods. The PET TeMs-g-PS-g-PAA exhibited good performance in separating water-oil emulsions with a high efficiency of more than 90% and flux for direct chloroform-water 2500 L m-2 h-1 and reverse emulsions of benzene-water 1700 L m-2 h-1. This method of preparing stimuli-responsive membranes with controlled wettability and responsiveness to environmental pH provides versatility in their use in separating two types of emulsions: direct and reverse.

Effect of copper doping on the photocatalytic performance of Ni2O3@PC membrane composites in norfloxacin degradation.

In this study, copper (Cu) and nickel oxide (Ni2O3) microtubes (MTs) were synthesized using an electroless template deposition technique within porous polycarbonate (PC) track-etched membranes (TeMs) to obtain Cu@PC and Ni2O3@PC composite membranes, respectively. The pristine PC TeMs featured nanochannels with a pore density of 4 × 107 pores per cm2 and an average pore diameter of 400 ± 13 nm. The synthesis of a mixed composite, combining Cu and Ni2O3 within the PC matrix, was achieved through a two-step deposition process using a Ni2O3@PC template. An analysis of the resultant composite structure (Cu/Ni2O3@PC) confirmed the existence of CuNi (97.3%) and CuO (2.7%) crystalline phases. The synthesized catalysts were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD) analysis, and atomic force microscopy (AFM). In photodegradation assessments, the Cu/Ni2O3@PC mixed composite demonstrated higher photocatalytic activity, achieving a substantial 59% degradation of norfloxacin (NOR) under UV light irradiation. This performance surpassed that of both Ni2O3@PC and Cu@PC composites. The optimal pH for maximum NOR removal from the aqueous solution was determined to be pH 5, with a reaction time of 180 min. The degradation of NOR in the presence of these composites adhered to the Langmuir-Hinshelwood mechanism and a pseudo-first order kinetic model. The reusability of the catalysts was also investigated for 10 consecutive runs, without any activation or regeneration treatments. The Cu@PC membrane catalyst demonstrated a marked decline in degradation efficiency after the 2nd test cycle, ultimately catalyzing only 10% of NOR after the 10th cycle. In contrast, the Ni2O3@PC based catalyst demonstrated a more stable NOR degradation efficiency throughout all 10 runs, with 27% NOR removal observed during the final test. Remarkably, the catalytic performance of the Cu/Ni2O3@PC mixed composite remained highly active even after being recycled 4 times. The degradation efficiency exhibited a gradual reduction, with a 17% decrease after the 6th run and a cumulative 35% removal of NOR achieved by the 10th cycle. Overall, the findings indicate that Cu/Ni2O3@PC mixed composite membranes may represent an advancement in the quest to mitigate the adverse effects of antibiotic pollution in aquatic environments and hold significant promise for sustainable water treatment practices.

Evaluation and optimization of polycarbonate track-etched (PCTE) membranes for direct methanol fuel cells.

Direct methanol fuel cells (DMFCs) offer a promising power source by utilizing liquid-state methanol as fuel, providing easy storage and transportability. Currently, DMFCs commonly employ perfluorosulfonic acid membranes, such as the well-known Nafion membrane, as proton exchange membranes. However, perfluorosulfonic acid membranes have significant drawbacks in DMFCs, including a high crossover rate, substantial swelling, poor thermal stability, and elevated costs. The crossover of methanol fuel to the cathode side is particularly detrimental as it can poison the precious Pt catalyst, leading to damage in the fuel cell system. In this manuscript, we propose a non-ionic proton exchange membrane based on the polycarbonate track etched (PCTE) membrane. The aligned nanopores in pristine PCTE, with a regular diameter, facilitate proton passage while mitigating the crossover of methanol molecules. This results in satisfactory proton conductivity and selectivity comparable to that of the commercial Gore membrane. By adding a layer of graphene treated with oxygen plasma for 10 seconds, methanol permeation can be reduced by 16.44%, while achieving a 42.11% increase in proton conductivity compared to the commercial Gore membrane. Furthermore, PCTE material offers a more cost-effective alternative to Gore membrane, with a 18.37% lower swelling ratio and significantly higher stability. These characteristics make PCTE a promising choice for DMFCs, offering potential improvements in performance and cost-effectiveness.

Structure Evolution of Iron (Hydr)oxides under Nanoconfinement and Its Implication for Water Treatment.

In the development of nanoenabled technologies for large-scale water treatment, immobilizing nanosized functional materials into the confined space of suitable substrates is one of the most effective strategies. However, the intrinsic effects of nanoconfinement on the decontamination performance of nanomaterials, particularly in terms of structural modulation, are rarely unveiled. Herein, we investigate the structure evolution and decontamination performance of iron (hydr)oxide nanoparticles, a widely used material for water treatment, when confined in track-etched (TE) membranes with channel sizes varying from 200 to 20 nm. Nanoconfinement drives phase transformation from ferrihydrite to goethite, rather than to hematite occurring in bulk systems, and the increase in the nanoconfinement degree from 200 to 20 nm leads to a significant drop in the fraction of the goethite phase within the aged products (from 41% to 0%). The nanoconfinement configuration is believed to greatly slow down the phase transformation kinetics, thereby preserving the specific adsorption of ferrihydrite toward As(V) even after 20-day aging at 343 K. This study unravels the structure evolution of confined iron hydroxide nanoparticles and provides new insights into the temporospatial effects of nanoconfinement on improving the water decontamination performance.

Biosensing with Tailored Track-Etched Nanochannels

Inspired by the high sensitivity, efficiency and selectivity of biological ion channels, the development of solid-state nanochannel sensors has been at the forefront of nanotechnology research in the last years. Many researchers worldwide have concentrated their efforts on the development of artificial nanochannels that can mimic the features of biological ion channels. These synthetic nanostructures are based on abiotic materials which provide higher robustness, thermal stability, chemical versatility and mechanical resistance than their biological counterparts. Furthermore, synthetic nanochannels and specific surface functionalization strategies have enabled fine control over the geometry and charge distribution which yielded the ability to manipulate the flux of ions through the channel. This gave rise to the formation of nanochannel-based platforms with applications in (bio)sensing as well as other fields. The development of chemical- and biosensors requires a combination of reliable nanofabrication techniques and versatile surface modification strategies, which render high sensitivity and high selectivity, respectively [1].Tailored single polymer nanochannels are routinely fabricated by ion-track nanotechnology. Polymer films are first irradiated with individual swift heavy ions at the GSI UNILAC accelerator. Each ion generates a highly localized cylindrical damage zone along its trajectory. These so-called ion tracks are subsequently dissolved and enlarged in a chemical etching process. By selecting suitable etching conditions, geometry (cylindrical, conical or bullet-like) and size of the nanochannels can be adjusted. The nanochannel surface can then be functionalized by means of different chemical strategies to enhance the sensing capabilities.There are two main nanochannel sensing techniques, ion current rectification (ICR) and resistive-pulse sensing (RPS). Both are affected by the geometry and surface charge of the nanochannel and based on measuring the change in ion current flowing through the channel induced by the chosen analyte [2]. In both approaches, the presence of a target analyte triggers a variation in the physicochemical properties of the channel which can be related to measurable changes in the transmembrane current, and is proportional to the analyte concentration.In this contribution, we will present nanochannel sensing platforms based on several single polymer channels fabricated by ion-track nanotechnology and a selection of surface functionalization strategies applied to the nanochannels. We will then discuss selected examples recently obtained with these tailored functionalized nanochannels and demonstrate selective and sensitive sensing applications based on both the ICR and RPS phenomena.[1] Toum Terrones, Y., Cayón, V. M., Laucirica, G., Cortez, M. L., Toimil-Molares, M. E., Trautmann, C., ... & Azzaroni, O. (2022). Ion Track-Based Nanofluidic Biosensors. In Miniaturized Biosensing Devices: Fabrication and Applications (pp. 57-81). Singapore: Springer Nature Singapore.[2] Kaya, D., & Keçeci, K. (2020). Track-etched nanoporous polymer membranes as sensors: A review. Journal of The Electrochemical Society, 167(3), 037543.

Molecular Detection of Multidrug Resistance and Characterizations of Mutations in Mycobacterium Tuberculosis Using Polycarbonate Track-Etched Membrane Based DNA Bio-Chip.

With the widespread use of rifampicin (RMP) and isoniazid (INH), multidrug resistance (MDR) in Mycobacterium tuberculosis (M.tb) poses a threat to the success of tuberculosis (TB) control programs. We have developed a new polycarbonate track-etched membranes(PC-TEM) based DNA bio-chip designed for rapid detection of mutations conferring MDR inM.tbculture isolates. Bio-chips were designed to contain 14 specific probes for wild type and mutated allele of selected codons within 80bprifampicin resistance determining region of rpoB gene, katGgene andmabA-inhAregulatory region. RMP-resistance-associated gene mutation pointsrpoB 516, 526, 531and533, and the INH-resistance-associated gene mutation pointskatG315andinhA-15were targeted. Bio-chip signal was detected using enhanced chemiluminescence. A total of 50 culture isolates that were sensitive or resistant to RMP and/or INH were analyzed by bio-chip. The results of culture-based drug susceptibility testing (DST)were used as the gold standard and gene sequencing was performed to resolve the discordance. Amongst 50 culture isolates, we have detected 18 MDR, 9 RMP mono-resistant, 6 INH mono-resistant, and 17 fully susceptible isolates. The developed DNA bio-chip has a sensitivity of 90% for RMP and MDR and 100% for INH resistance. The bio-chip has a specificity of 100% for RMP and MDR and 88.8% for INH detection. The identification of mutations using the DNA bio-chip was 100% concordant with the sequencing data for the probes covered by the bio-chip. The detection ofrpoB, katGand inhA gene mutation points by a DNA bio-chip may be used as a rapid, accurate, and economical, clinical detection method for MDR detection in M.tb. This is very valuable for the control of TB epidemics.

Element Composition of Fractionated Water-Extractable Soil Colloidal Particles Separated by Track-Etched Membranes

Membrane fractionation with track-etched membranes was used to size-profile the microelement composition of water-extractable soil colloids (WESCs). The aim of the study is the element composition of narrow WESC fractions of typical chernozems in the range of 0.01–10 µm. Micro-/ultrafiltration through a cascade of track-etched polycarbonate membrane filters with pore sizes of 5, 2, 1, 0.8, 0.4, 0.2, 0.1, 0.05, 0.03, and 0.01 µm at room temperature was used. ICP–AES using direct spraying of obtained fractions without decomposition was used; Al, Ba, Cd, Cr, Cu, Fe, Mn, Si, Sr, Ti, Zn, Ca, K, Mg, Na, P, and S were found. Narrow WESC fractions differ significantly. For macro- and microelements, maximum amounts of Si, Al, Fe, and Ti and their maximum percentages are observed in fractions with sizes above 1 µm, while Ca, Mg, Mn, Cu, Zn, K, and S are accumulated more in fractions with sizes below 1 µm. The developed approach provides preparative isolation of a detailed set of narrow WESC fractions in the micrometer–nanometer range. This provides element soil profiles that reveal distinct differences and the individual character of each fraction as well as trends in changes in the mineral matrix and microelement composition with fraction size.

Development of high-integrity reverse osmosis membranes for enhanced removal of microorganisms

Improved integrity of reverse osmosis (RO) membranes for pathogenic microorganisms can enhance the microbiological safety of potable water reuse. This study aimed to produce a high-integrity RO membrane that is less prone to defects or failures of the polyamide skin layer. The commercial track-etched (TE) microfiltration membranes with uniform pore sizes of 0.2 μm were adopted as a robust support layer. The polyamide skin layer was successfully formed by creating a thin m-phenylenediamine (MPD) layer using a spin coater before the interfacial polymerization. The best TE-based RO membranes had a pure water permeability of 1.1 L/m2hbar and a salt rejection of 97 %. The field emission scanning electron microscopy revealed that the skin layer thickness of the TE-based membrane (approx. 31 nm) was equivalent to a commercial RO membrane. The removal of bacteria-sized particles (0.5 μm fluorescent microspheres) by the fabricated TE-based membrane (8.6-log) was greater than that by the commercial RO membrane taken out from an RO membrane element (7.8-log). Although complete removal of bacteria-sized particles was not achieved with small TE-based RO membrane coupons, this study established a viable protocol for producing a high-integrity RO membrane by forming the polyamide skin layer on the TE support layer.

Highly enantioseparation in membrane-supported one-dimensional metal–organic framework hollow nanotube array prepared via mussel-inspired chemistry

High-enantioselective chiral metal–organic framework (CMOF) nanochannel membranes are of critical importance for chiral enantiomeric separations by taking advantage of their inherent high porosity and intrinsic chirality. However, traditional chiral membranes are still constrained by the permeability-selectivity trade-off, making it challenging to improve both simultaneously. This study described the structure of a new class of membrane-supported one-dimensional MOF hollow nanotube for transport and separation of chiral 1-phenylethanol (PE), utilizing a biomimetic polydopamine (PDA)-mediated counter-diffusion synthesis strategy. The inner cylindrical pore channel surface of polycarbonate track-etched membranes (PCTM) was modified by PDA chemistry to control the nucleation and interfacial growth of CMOF crystals, leading to the development of integrated chromatographic micro-column array membranes PCTM@PDA@Cu2C2D and PCTM@PDA@Cu2C2B with one-dimensional (1D) CMOF hollow nanochannels. Compared to PCTM@PDA@Cu2C2B, it was highlighted that the chiral membrane PCTM@PDA@Cu2C2D possessed the higher loading of Cu2C2D functional layer and more suitable steric chiral microenvironment, thus exhibited more outstanding permeability and selectivity for S-PE enantiomer with an enantiomeric excess value up to 90 % under an optimal guest concentration of 250 ppm at 30 °C for 1 h. The chiral membrane with 1D MOF hollow nanotubes, created by applying a gentle and simple method to introduce CMOF into the surface and pore channels of the substrate membrane, was expected to be utilized for the large-scale production of chiral separation membranes for industrial applications.

A thin-film polymer heating element with a continuous silver nanowires network embedded inside

This study presents a method for fabricating a film-based heating element using a polymer material with an array of intersecting conductive elements embedded within it. Track-etched membranes (TM) with a thickness of 10 μm were used as the template, and their pores were filled with metal, forming a three-dimensional grid. Due to the unique manufacturing process of TM, the pores inside intersect with each other, allowing for contacts between individual nanowires (NWs) when filled with metal. Experimental results demonstrated that filling the TM pores with silver allows for heating temperatures up to 78 degrees without deformation or damage to the heating element. The resulting flexible heating element can be utilized in medical devices for heating purposes or as a thermal barrier coating.