Polypropylene Membrane Research Articles

Inhibitory activity of some short-chain aliphatic aldehydes on pheromone and ammonium carbonate-mediated attraction in olive fruit fly, Bactrocera oleae.

The olive fruit fly (OFF), Bactrocera oleae (Rossi), is the main insect pest of olive trees worldwide. Legislation limits to the use of some synthetic larvicidal insecticides is leading to the development of new control options for preventive control of adult flies. In the present study, the biological activity of four short-chain aliphatic aldehydes, namely hexanal, (E)-2-hexenal, heptanal and (E)-2-heptenal, previously reported as repellents to the OFF adults was investigated. Electroantennography (EAG) recordings showed that antennae of OFF males and females are able to perceive the test compounds in a wide range of doses. In field trapping experiments, reservoir-type polypropylene (PP) membrane dispensers loaded with individual compounds did not elicit a significant attraction of OFF males and females. On the contrary, a significant reduction of male catches was noticed when sex pheromone dispensers and PP membrane dispensers, loaded with one of the test compounds, were applied on the same white sticky traps ≈20 cm apart. Likewise, male and female catches in yellow sticky traps baited with ammonium carbonate (AC) dispensers as food attractant were significantly reduced by the presence of PP membrane dispensers of individual aliphatic aldehydes on the same traps. In small plots control trials, solid formulations of the four aldehydes into a bentonite clay support induced a significant reduction of the OFF active infestation mainly when C6 and C7 aldehyde-activated bentonites were used. Short-chain aliphatic aldehydes showed inhibitory effects on sex pheromone and food attractant-mediated attraction of OFF. Results of field trials suggest potential of short-chain aliphatic aldehydes to develop new semiochemical-based OFF control options. © 2024 Society of Chemical Industry.

Polypropylene membrane with gradient-distributed covalent organic framework for highly efficient blood oxygenation

Hollow fiber membrane (HFM) is widely used for extracorporeal membrane oxygenator (ECMO) because of large membrane area, high packing density, self-supporting structure and good flexibility. However, polymeric HFMs often suffer from a trade-off between gas permeability and anti-plasma leakage performance. In this study, HFMs with gradient structure were prepared by introducing COF-42 as fillers into the polypropylene (PP) matrix through surface segregation. The enriched COF-42 near the upper surface endowed the membrane a gradient structure to reduce the plasma leakage and improve gas permeability. Compared with PP membranes, PP/COF-42 oxygenation membranes retained good blood compatibility and higher mechanical properties. The PP/COF-42–0.5 HFMs exhibited O2 exchange rate of ∼ 342.6 ml min−1 m−2 and CO2 exchange rate of ∼ 989.6 ml min−1 m−2, which was about 218.7 % and 15.4 % larger than that of the PP HFMs, respectively. Moreover, the simulated plasma leakage time could reach 124 h, which was about 21 times longer than that of PP HFMs. The membranes exhibited excellent blood oxygenation performance and anti-plasma leakage performance, which had great potential in ECMO.

Electron beam induced graft polymerized anti oil-fouling biaxial polypropylene membrane with harsh environment tolerance

The intrinsic hydrophobic behavior of biaxial-oriented polypropylene microporous membrane limits its broad application area by leading serious membrane fouling. An environment-friendly, practical, and facile to large-scale prepared surface modification process is designed to enhance the membrane wettability and oil-fouling. By employing electron beam radiation, acrylic acid, and polyvinyl alcohol in the pre-irradiation-induced graft polymerization process, a micro-nano structure was developed and the surface roughness was increased from 66.5 nm to 99.3 nm. Enhancing the grafting ratio further reduces the pore size of the final modified membrane from 54 nm to 25 nm, which is significantly smaller than the size of the emulsified oil droplet. By modifying the morphological and structural characteristics of the grafted membrane, excellent oil-fouling resistance features are attained with UWOCA value 161° and separation efficiency of 99.3 %. Moreover, the theoretical explanations for hydrophilicity and oil-fouling resistance of modified membranes are also developed using DFT calculations and the Hermia model, which shows alignment with experimental data. Consequently, considerable improvements in wettability, thermal and mechanical behavior are obtained by this facial surface modification approach, which could further broaden the modified membrane's applications area in membrane separation technology while lengthening its service life.

Electrochemical Extraction with Supported Liquid Membrane for Removing Copper from Synthetic Wastewater: Optimisation through Response Surface Methodology

In this study, copper was removed from an aqueous solution through electromembrane extraction (EME), a new approach that utilises a two-chamber electrochemical cell. It consists of two electrodes (stainless steel cathode and graphite anode) and a solid liquid membrane (SLM). SLM is composed of supporting polypropylene membrane impregnated with1-octanol as an organic solvent and bis(2-ethylhexyl) phosphate (DEHP) as a carrier. The effects of process parameters such as applied voltage, pH and copper concentration on the removal of copper were investigated. Response surface methodology (RSM) was applied to optimise these parameters and their interactions. Results indicated that pH has the major effect on the removal of copper, followed by applied voltage. The squared interaction term in the RSM model has the highest contribution (70.5%), followed by the linear term, thereby confirming the significant interaction among the variables. The optimum conditions include an applied voltage of 60V, pH of 5.18 and initial copper concentration of 5 ppm, which yield to a removal efficiency of 80% after 6 hours of operation. The findings demonstrate the use of electromembrane extraction as an efficient method for the removal of heavy metals and provide valuable insights for future application to other environmental and water treatment processes.

Cellulose-based multi-responsive soft robots for programmable smart devices

In the realm of advanced smart manufacturing, the development of fast, sensitive, stable soft robots that can be driven by multiple stimuli remains a significant challenge. In this study, we developed a cellulose-based soft robot featuring a dual-layer structure. The top layer is a hydrophilic composite membrane made from cellulose nanofibers (CNFs), MXene nanosheets, and carbon nanotubes (CNTs), henceforth referred to as the CNF@MXene-CNT (CMN) composite membrane, while the bottom layer consists of a hydrophobic Biaxially Oriented Polypropylene (BOPP) membrane. The soft robot exhibits highly sensitive and fast response towards humidity-, natural light and electrothermal stimuli, which can be attributed to the high humidity expansion (0.0005 (%RH)-1), photothermal conversion, and electrical thermal conversion of CMN composite membrane, also the distinctive expansion characteristics of CMN (−0.000757 °C−1) and BOPP (0.000137 (°C)-1). Remarkably, the soft robot can be actuated with merely 67 mW cm−2 of natural light or a power supply of 2.8 V, achieving a bending range of 360° with a corresponding bending curvature of 2.67 cm−1. The soft robot’s motion state and speed can be meticulously controlled, further emphasizing their vast applicability in various fields, including medical, industrial, aerospace, and beyond. The soft robot has been applied as a smart curtain, intelligent optical switch, and electrically controlled robot, demonstrating its exceptional multifunctionality and wide ranges of applications.

Ultrathin titanium carbide-modified separator for high-performance lithium–sulfur batteries

Despite a high theoretical capacity, the practical application of lithium-sulfur batteries has been primarily limited by the migration of long-chained polysulfide species during the charge/discharge processes. One effective approach to address the issues is to design a functional separator or interlayer. Here, we prepared a modified separator with an ultrathin layer of titanium carbide (TiC) using radio-frequency sputtering on a commercial Celgard polypropylene membrane. The 240-nm TiC coating layer can enhance the interfacial properties of Celgard separators in porosity, wettability, roughness, etc. Hence, via experimental and theoretical investigation, we discovered that TiC can efficiently adsorb polysulfides and boost charge transfer via strong covalent C–S bonds. Using a TiC-modified separator can impede the shuttle effect and improve the kinetics of sulfur conversion reactions. Thus, the Li–S batteries with TiC separator deliver excellent electrochemical performances with a good rate capability (717 mAh g−1 at 7.0C) and an ultra-low decay rate of 0.058 % per cycle over 800 cycles at a C-rate of 2.0C. Furthermore, a high areal capacity of 4.3 mAh cm−2 was achieved with a high mass-loading of sulfur cathode up to 7.0 mg cm−2.

Addition of a Polar, Porous Phase-Inversion-PVDF Membrane to Lithium–Sulfur Cells (LSBs) Already with a Microporous Polypropylene Separator Enhances the Battery Performance

Lithium–sulfur batteries (LSBs) are widely studied as an alternative to lithium-ion batteries, this emphasis being due to their high theoretical energy density and low cost, and to the high natural abundance of sulfur. Lithium polysulfide shuttling and lithium dendrite growth have limited their commercialization. Porous polyvinylidene fluoride (PVDF) separators have shown improved performance (relative to hydrocarbon separators) in lithium-ion batteries due to faster lithium-ion migration and higher Li+ transference number. A thin polar PVDF membrane has now been fabricated via phase inversion (an immersion-precipitation method) yielding a β (polar) phase concentration of 72%. Preparation from commercial PVDF used dimethylformamide (DMF) solvent at the optimized crystallizing temperature of 70 °C, and pores in the membrane were generated by exchange of DMF with deionized water as non-solvent. The polar PVDF film produced has the advantages of being ultrathin (15 µm), lightweight (1.15 mg cm−2), of high porosity (75%) and high wettability (84%), and it shows enhanced thermal stability relative to polypropylene (PP). The porous, polar PVDF membrane was combined with a commercially available PP membrane to give a hybrid, two-layer, separator combination for LSBs. A synergy was created in the two-layer separator, providing high sulfur utilization and curbing polysulfide shuttling. The electrochemical performance with the hybrid separator (PP–β-PVDF) was evaluated in LSB cells and showed good cyclability and rate capability: those LSB cells showed a stable capacity of 750 mA h g−1 after 100 cycles at 0.1 C, much higher than that for otherwise-identical cells using a commercial PP-only separator (480 mA h g−1).

Characterization of anisotropic pore structure and dense selective layer of capillary membranes for long-term ECMO by cross-sectional ion-milling method.

Since the COVID-19 pandemic of 2020-2023, extracorporeal membrane oxygenator (ECMO) has attracted considerable attention worldwide. It is expected that ECMO with long-term durability is put into practical use in order to prepare for next emerging infectious diseases and to facilitate manufacturing for novel medical devices. Polypropylene (PP) and polymethylpentene (PMP) capillary membranes are currently the mainstream for gas exchange membrane for ECMO. ECMO support days for COVID-19-related acute hypoxemic respiratory failure have been reported to be on average for 14 or 24days. It is necessary to improve opposing functions such that promoting the permeation of oxygen and carbon dioxide and inhibiting the permeation of water vapor or plasma to develop sufficient durability for long-term use. For this purpose, accurately controlling the anisotropy of the pore structure of the entire cross section and functions of capillary membrane is significant. In this study, we focused on the cross-sectional ion-milling (CSIM) method, to precisely clarify the pore structure of the entire cross section of capillary membrane for ECMO, because there is less physical stress on the porous structure applied during the preparation of cross-sectional samples of porous capillary membranes. We attempted to observe the cross sections of commercially available PMP membranes using the CSIM method. As a result, we succeeded in fabricating fine-scale flat cross-sectional samples of PMP capillary membranes. The pore structures and the degree of anisotropy of the cross sections are quantitatively clarified. The achievements and the approaches of this study are being applied to the development of next-generation gas exchange membranes.

Dairy wastewater treatment with direct-contact membrane distillation in Oman

Direct contact membrane distillation (DCMD) process was implemented for treating dairy wastewater (DWW) from an Omani dairy industry. Commercial polytetrafluoroethylene (PTFE) and polypropylene (PP) membranes were tested under different temperatures. The aim of this study in to investigate the potential of pure water production rejecting salts, volatile and non-volatile organic compounds present in DWW. Using laboratory techniques such as gas chromatography, we inspected permeate composition, identifying both volatile and non-volatile organic matter. Comprehensive characterization of membrane surface properties via Fourier-transform Infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and Thermal Gravimetric analysis (TGA) provided critical insights. Findings revealed the denaturation of proteins at 60 °C, leading to significant pore blockage and a consequential 50.3 % reduction in flux. Impressively, the membranes achieved rejection rates of 89–99 % for non-volatile organic matter, while completely rejecting D-limonene. However, traces of volatile fatty acids were detected in the permeate. Elemental analysis exposed the presence of various dairy-derived elements at the membrane surface. FTIR peaks highlighted distinct functional groups of dairy components, while TGA affirmed the accumulation of dairy aggregates with rising temperature. These findings underscore membrane distillation's competence in dairy wastewater treatment, presenting a compelling case for its widespread application in environmental remediation endeavors.

Construction of robust silica-titania polydopamine composite membrane with light-absorption property for photothermal vacuum membrane distillation

A robust silica-titania polydopamine composite membrane was fabricated adding a photothermal polydopamine coating to the surface of polypropylene membrane for photothermal vacuum membrane distillation. Detailly, the surface of an inert PP membrane was modified with atomically controllable titanium and silicon to enhance the hydroxyl groups on the membrane surface, then, a photothermal effect layer of polydopamine was generated on the composite membrane surface through the self-polymerization reaction of dopamine. The polydopamine coating has significant light absorption and heating properties, and it can act as a local heater when exposed to light sources. This local heating effect significantly raises the temperature at the membrane interface, creating a thermal gradient that drives the evaporation of water molecules. Specifically, we quantitatively analyzed the three reasons (surface energy, free radicals, and photothermal effect) for the increase in evaporation rate of the pristion PP membrane caused by the membrane composite membrane. Among these reasons, the photothermal effect caused by black polydopamine is the most important factor for improving evaporation efficiency. The dark-illumination alternating experiment revealed that the PP-TiO2-SiO2-PDA composite membrane delivered a noteworthy enhancement in vacuum membrane distillation performance (approximately 40%), while the improvement of the PP membrane was only 1.7%.

A switchable dual-mode film with designed intercalated and hierarchical structures for highly efficient passive radiation cooling and solar heating

A single-mode solar heating (SH) and passive radiative cooling (PRC) have been fast developed in outdoor thermal management. However, they hardly change with the temperature fluctuations of the hot and cold seasons. Herein, a flexible and stable dual-mode film with photo responsibility was engineered by integrating heating coating and cooling coating on the opposite surfaces of a porous polypropylene (PP) membrane. Flip the surfaces of the dual-mode film-facing solar light to switch between PRC and SH. The cross-linked heating side was fabricated from reduced graphene oxide (rGO) nanosheets intercalated with carbon black (CB) particles via spraying. A thick intercalated film can enhance solar absorptivity (96.4 %) and low infrared emissivity (8.0 %) due to the multiple solar reflections and adsorption between the interlayers, leading to high solar heating. The cooling side was derived from polyvinylidene fluoride (PVDF) coating embedded micro-nano Al2O3 particles via water vapor-induced phase separation (VIPS). The hierarchical coating with a pore size of 8.4 ± 0.1 µm and roughness of 4.0 ± 0.3 µm exhibits high solar reflectivity (92.2 %) and infrared emissivity (96.9 %), resulting in excellent passive radiative cooling. The net heating power (Pheating) and net cooling power (Pcooling) of the dual-mode film are 845.9 and 96.7 W m−2. Moreover, the dual-mode film exhibits outdoor thermoregulation capacity upon covering buildings, cars, and ice. In outdoor environments under solar radiation of 611 ∼ 716 W m−2, it has a temperature increase/decrease of 17.8/5.3 °C to the ambient temperature. Owing to the scalable fabrication processes and excellent thermoregulation characteristics, the dual-mode film is promising for applications in personal thermal management, energy-efficient buildings, in-car temperature control, and food freezing-thawing.

Comprehensive clinical and histological evaluation of bovine hydroxyapatite bone graft with polypropylene membrane versus leukocyte- and platelet-rich fibrin for alveolar preservation after tooth extraction.

Osseointegrated implant placement in the ideal prosthetic position necessitates a sufficient residual alveolar ridge. Tooth extraction and the subsequent healing process often lead to bony deformities, characterized by a reduction in alveolar ridge height and width, resulting in unfavorable ridge architecture for dental implant placement. Several materials, including allografts, alloplastics, xenografts, and autogenous bone, are commonly used to address these concerns. In this context, leucocyte- and platelet-rich fibrin (L-PRF) emerges as a promising solution. This case report aims to compare the clinical and histological efficacy of bovine hydroxyapatite bone graft covered with polypropylene membrane (BHAG-PM) and leucocyte- and platelet-rich fibrin (L-PRF) in preserving dental alveoli following tooth extraction. Extraction, graft placement in the alveoli, and the anterior border between extracted elements were performed for both treatment groups. Up to 24 months of follow-up revealed satisfactory and comparable clinical and histological outcomes. These results suggest that both BHAG-PM and L-PRF effectively promote alveolar preservation, paving the way for ideal implant placement. In general, bone-substitute materials are effective in reducing alveolar changes after tooth extraction. Xenograft materials should be considered as among the best of the available grafting materials for alveolar preservation after tooth extraction. Both techniques effectively preserve the alveolar bone and facilitate the placement of osseointegrated implants in ideal positions, paving the way for successful oral rehabilitation.

Production of Disinfective Coating Layer to Facial Masks Supplemented with Camellia sinensis Extract.

Although usefulness of masks for protection against respiratory pathogens, accumulation of pathogens on their surface represents a source of infection spread. Here we prepared a plant extract-based disinfecting layer to be used in coating masks thus inhibiting their capacity to transmit airborne pathogens. To reach this, a polypropylene membrane base was coated with a layer of polyvinyledine difluoride polymer containing 500μg/ml of Camellia sinensis (Black tea) methanolic extract. Direct inhibitory effects of C. sinensis were initially demonstrated against Staphylococcus aureus (respiratory bacteria), influenza A virus (enveloped virus) and adenovirus 1 (non-enveloped virus) which were directly proportional to both extract concentration and incubation time with the pathogen. This was later confirmed by the capacity of the supplemented membrane with the plant extract to block infectivity of the above mentioned pathogens, recorded % inhibition values were 61, 72 and 50 for S. aureus, influenza and adenovirus, respectively. In addition to the disinfecting capacity of the membrane its hydrophobic nature and pore size (154nm) prevented penetration of dust particles or water droplets carrying respiratory pathogens. In summary, introducing this layer could protect users from infection and decrease infection risk upon handling contaminated masks surfaces.

Evaluation of polypropylene microporous membranes as extraction devices for determination of carcinogenic aromatic amines in smoker urine by GC–MS/MS

Exposure to tobacco smoke is highly correlated to the incidence of different types of cancer due to various carcinogenic compounds present in such smoke. Aromatic amines, such as 1-naphthylamine (1-NA) and 2-naphthylamine (2-NA), are produced in tobacco burning and are linked to bladder cancer. Miniaturized solid phase extraction techniques, such as microporous membrane solid phase extraction (MMSPE), have shown potential for the extraction of aromatic compounds. In this study, a bioanalytical method for the determination of 1-NA and 2-NA in human urine was developed using polypropylene microporous membranes as a sorptive phase for MMSPE. Urine samples were hydrolyzed with HCl for 1 h at 80 °C, after which pH was adjusted to 10. Ultrasound-assisted MMSPE procedure was optimized by factorial design as follows. To each sample, 750 µL of methanol was added, and ultrasound-assisted MMSPE was conducted for 1 h with four devices containing seven 2 mm polypropylene membrane segments. After extraction, the segments were transferred to 400 µL of hexane, and desorption was conducted for 30 min. Extracts were submitted to a simple and fast microwave-assisted derivatization procedure, by the addition of 10 µL of PFPA and heating at 480 W for 3 min, followed by clean-up with phosphate buffer pH 8.0 and GC–MS/MS analysis. Adequate linearity was obtained for both analytes in a range from 25 to 500 µg L−1, while the multiple reaction monitoring approach provided satisfactory selectivity and specificity. Intra-day (n = 6) and inter-day (n = 5) precision and accuracy were satisfactory, below 15 % and between 85 and 115 %, respectively. Recovery rates found were 91.9 and 58.4 % for 1-NA and 2-NA, respectively, with adequate precision. 1-NA was found in first-hand smokers’ urine samples in a concentration range from 20.98 to 89.09 µg in 24 h, while it could be detected in second-hand smoker's urine samples, and 2-NA detected in all first and second-hand smokers’ urine samples. The proposed method expands the applicability of low cost MMSPE devices to aromatic amines and biological fluids.

Polypropylene membranes prepared via non-solvent/thermally induced phase separation: Effect of non-solvent nature

The goal of this work was to investigate the effect of non-solvent nature on the formation of porous membranes via non-solvent/thermally induced phase separation (N-TIPS). The hot solution of polypropylene (PP) in a mixture of dioctyl phthalate (DOP) and dibutyl phthalate (DBP) at 210 °C was placed as a thin film on a polyethylene terephthalate (PET) substrate, and then precipitated by immersion in the non-solvent (water, iso-propanol, 1-hexanol, or 1-decanol) at room temperature. It was found that the non-solvent nature greatly affected the morphology of the thin skin layer of the membrane facing the precipitation bath, which can be attributed to non-solvent induced phase separation (NIPS). The affinity between the polymeric solution and corresponding non-solvent was evaluated by using Hansen solubility parameters of components taken at room temperature and extrapolated to the temperature of 210 °C. An increase in the affinity between the non-solvent and the polymer transformed the surface layer structure from almost monolithic to cellular (with different pore sizes and porosity) and to spherulitic types. The non-solvent nature played a less pronounced role in the formation of the porous structure of the membrane bulk and the back side of the membrane (facing the PET substrate). Since the morphology of the rest of the membrane was correlated with thermophysical properties of non-solvents, it was concluded that the membrane formation took place due to temperature induced phase separation (TIPS). In the case of water, which has the highest cooling rate, the polypropylene crystallized by forming a “smectic” structure, while the standard α-lamellar structure was observed for other non-solvents. To gain insight into the TIPS process, a model of unsteady one-dimensional heat transfer was applied to simulate the change in the temperature profile of the hot, thin film of polymeric solution placed in the corresponding non-solvent. The resulting membranes were mainly in the microfiltration range with a mean through pore size of 0.05–0.61 μm, and iso-propanol permeance of 2.1–8.4 m3 m−2∙h−1∙bar−1. The rejection of 500 nm polystyrene microspheres was in the range of 45–98 %. The tensile strength was in the range of 2.9–3.2 MPa, and elongation at break was 30–190 % with respect to the non-solvent used.

Water Proofing System in Concrete Structures

Water proof structure is a design concept that aims to repel water and prevent any moisture from seeping into the materials used in construction. This type of structure is particularly important in areas prone to heavy rainfall or flooding, as it helps maintain the integrity and durability of the building. Water proof concrete is formulated with additives and admixtures that create a barrier against water infiltration, making it ideal for areas prone to high levels of humidity or moisture. By incorporating this technology into construction projects, builders can ensure that their structures remain protected from the damaging effects of moisture, such as mold growth, deterioration of building materials, and potential structural issues. The use of abstract damp proof concrete represents a forward-thinking approach to building design and can greatly enhance the durability and longevity of a building.Crystalline admix water proofing with water stops, water proofing with Atactic Polypropylene membrane, and injection are the water proofing systems most commonly used in basements. Using non-shrinking cementitious grout for waterproofing, concrete must have crystalline admixtures made of cementitious powder and water. For toilets in non-sunken places, water proofing with an elastomeric cementitious coating is used. In sunken areas, brick jelly cement concrete with inherent water proofing compound is used.In this paper it deals with the different types of water proofing system..

NiFe-LDH/nylon 6 composite electrospun on polypropylene membrane: A new extractive device development for porous membrane protected micro-solid-phase extraction of organophosphate pesticides from fresh fruit juice samples coupled with liquid chromatography tandem mass analysis

A unique strategy for developing porous membrane protected micro-solid phase extraction has been provided. An electrospun composite was fabricated on the sheet of membrane. To this end, NiFe-layered double hydroxide/Nylon 6 composite nanofibers were coated on a polypropylene membrane sheet followed by folding into a pocket shape, which were then utilized as a novel extractive device to extract of organophosphorus pesticides from fresh fruit juice samples prior to liquid chromatography–tandem mass spectrometry (LC–MS/MS) analysis. The fabricated hybrid composites were successfully characterized. The effective parameters on extraction performance were investigated. LODs were 0.020–0.065 ng mL−1. Excellent linearity (R2≥0.996) was observed between 0.05 and 100.0 ng mL−1. RSDs% were in the range of 3.1–5.8% (intra-day, n = 3) and 2.6–5.5% (inter-day, n = 3×3). Satisfactory related recovery values within the acceptable range of 90.7–111.2% with RSDs% below 6.7% were achieved for the analysis of real samples.

Exploring the impact of polyvinylidenefluoride membrane physical properties on the enrichment efficacy of microfluidic electro-membrane extraction of acidic drugs

Membrane technology has revolutionized various fields with its energy efficiency, versatility, user-friendliness, and adaptability. This study introduces a microfluidic chip, comprised of silicone rubber and polymethylmethacrylate (PMMA) sheets to explore the impacts of polymeric support morphology on electro-membrane extraction efficiency, representing a pioneering exploration in this field. In this research, three polyvinylidenefluoride (PVDF) membranes with distinct pore sizes were fabricated and their characteristics were assessed through field-emission scanning electron microscopy (FESEM), and atomic force microscopy (AFM). This investigation centers on the extraction of three widely prescribed non-steroidal anti-inflammatory drugs: aspirin (ASA), naproxen (NAP), and ibuprofen (IBU). Quantitative parameters in the extraction process including voltage, donor phase flow rate, and acceptor phase composition were optimized, considering the type of membrane as a qualitative factor. To assess the performance of the fabricated PVDF membranes, a comparative analysis with a commercially available Polypropylene (PP) membrane was conducted. Efficient enrichment factors of 30.86, 23.15, and 21.06 were attained for ASA, NAP, and IBU, respectively, from urine samples under optimal conditions using the optimum PVDF membrane. Significantly, the choice of the ideal membrane amplified the purification levels of ASA, NAP, and IBU by factors of 1.6, 7.5, and 40, respectively.

Deciphering the Performance Enhancement, Cell Failure Mechanism, and Amelioration Strategy of Sodium Storage in Metal Chalcogenides-Based Andes.

Transition metal chalcogenides (TMCs) emerge as promising anode materials for sodium-ion batteries (SIBs), heralding a new era of energy storage solutions. Despite their potential, the mechanisms underlying their performance enhancement and susceptibility to failure in ether-based electrolytes remain elusive. This study delves into these aspects, employing CoS2 electrodes as a case in point to elucidate the phenomena. The investigation reveals that CoS2 undergoes a unique irreversible and progressive solid-liquid-solid phase transition from its native state to sodium polysulfides (NaPSs), and ultimately to a Cu1.8S/Co composite, accompanied by a gradual morphological transformation from microspheres to a stable 3D porous architecture. This reconstructed 3D porous structure is pivotal for its exceptional Na+ diffusion kinetics and resilience to cycling-induced stress, being the main reason for ultrastable cycling and ultrahigh rate capability. Nonetheless, the CoS2 electrode suffers from an inevitable cycle life termination due to the microshort-circuit induced by Na metal corrosion and separator degradation. Through a comparative analysis of various TMCs, a predictive framework linking electrode longevity is established to electrode potential and Gibbs free energy. Finally, the cell failure issue is significantly mitigated at a material level (graphene encapsulation) and cell level (polypropylene membrane incorporation) by alleviating the NaPSs shuttling and microshort-circuit.

Organic Solvent-Based Li–Air Batteries with Cotton and Charcoal Cathode

We report on the construction and investigation of Li–air batteries consisting of a charcoal cathode and cotton texture soaked with different organic solvents containing a lithium triflate (LiOTf) electrolyte. Charcoal was found to be an appropriate cathode for Li–air batteries. Furthermore, cycling tests showed stable operation at over 800 cycles when dimethyl sulfoxide (DMSO) and diethylene glycol dimethyl ether (DEGME) were used as solvents, whereas low electrochemical stability was observed when propylene carbonate was used. The charging, discharging, and long-term discharging steps were mathematically modeled. Electrochemical impedance spectroscopy showed Gerischer impedance, suggesting intensive oxygen transport at the surface of the charcoal cathode. Diffusion, charge transfer, and solid electrolyte interphase processes were identified using distribution of relaxation time analysis. In the polypropylene (PP) membrane soaked with LiOTf in DEGME, three different states of Li ions were identified by 7Li-triple-quantum time proportional phase increment nuclear magnetic resonance measurements. On the basis of the latter results, a mechanism was suggested for Li-ion transport inside the PP membrane. The activity of the charcoal cathode was confirmed by Raman and cyclic voltammetry measurements.