Search Results (132)

This study explores using polyvinylidene fluoride (PVDF) membranes modified with multi-walled carbon nanotubes (MWCNTs) to treat simulated and industrial brine from coal power stations. The MWCNTs were acid-treated and characterized using Fourier Transform Infrared Spectroscopy (FTIR), Raman, and nitrogen sorption at 77 K, Thermogravimetric analysis (TGA), and Transmission electron microscopy (TEM). The desired membranes were obtained by casting from a solution of N-Methyl-2-pyrrolidone, PVDF, various weight percentages of MWCNTs, and a small amount of polyvinylpyrrolidone. The acid treatment of the MWCNTs introduced oxygen moieties on the surface, and increased pore volume and surface area while maintaining crystallinity and structural integrity remain preserved. The maximum rejection rate achieved was 41.82% with 1 wt.% of acid-treated MWCNTs in the PVDF membrane. Acid-treated MWCNTs loaded membranes had an improved rejection rate, which was 5× higher than membranes without MWCNTs. Full article

Planar heaters are designed to deliver uniform heat across broad surfaces and serve as critical components in applications requiring energy efficiency, safety, and mechanical flexibility, such as wearable electronics and smart textiles. However, conventional metal-based heaters are limited by poor adaptability to curved or complex surfaces, low mechanical compliance, and susceptibility to oxidation-induced degradation. To overcome these challenges, we applied a protein-assisted electroless copper (Cu) plating strategy to electrospun poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) nanofiber substrates to fabricate flexible, conductive planar heating membranes. For interfacial functionalization, a protein-based engineering approach using bovine serum albumin (BSA) was employed to facilitate palladium ion coordination and seed formation. The resulting membrane exhibited a dense, continuous Cu coating, low sheet resistance, excellent durability under mechanical deformation, and stable heating performance at low voltages. These results demonstrate that the BSA-assisted strategy can be effectively extended to complex three-dimensional fibrous membranes, supporting its scalability and practical potential for next-generation conformal and wearable planar heaters. Full article

Background/Objectives: Airborne viral diseases pose a health risk, due to which there is a growing interest in developing filter materials capable of capturing fine particles containing virions from the air and that also have a virucidal effect. Nanofiber membranes made of poly(vinylidene fluoride) dissolved in N,N-dimethylacetamide and functionalized with copper, silver, and zinc nanoclusters were fabricated via electrospinning. This study aims to evaluate and compare the virucidal effects of nanofibers functionalized with metal nanoclusters against the human influenza A virus A/WSN/1933 (H1N1) and SARS-CoV-2. Methods: A comprehensive characterization of materials, including X-ray diffraction, scanning electron microscopy, microwave plasma atomic emission spectroscopy, thermogravimetric analysis, contact angle measurements, nitrogen sorption analysis, mercury intrusion porosimetry, filtration efficiency, and virucidal tests, was used to understand the interdependence of the materials’ physical characteristics and biological effects, as well as to determine their suitability for application as antiviral materials in air filtration systems. Results: All the filter materials tested demonstrated very high particle filtration efficiency (≥98.0%). The material embedded with copper nanoclusters showed strong virucidal efficacy against the SARS-CoV-2 alpha variant, achieving an approximately 1000-fold reduction in infectious virions within 12 h. The fibrous nanowire polymer functionalized with zinc nanoclusters was the most effective material against the human influenza A virus strain A/WSN/1933 (H1N1). Conclusions: The materials with Cu nanoclusters can be used with high efficiency to passivate and kill the SARS-CoV-2 alpha variant virions, and Zn nanoclusters modified activated porous membranes for killing human influenza A virus A7WSN/1933 (H1N1) virions. Full article

Fibrous structure is a promising building block for developing high-performance wearable piezoresistive sensors. However, the inherent non-conductivity of the fibrous polymer remains a bottleneck for highly sensitive and fast-responsive piezoresistive sensors. Herein, we reported a polyaniline/reduced graphene oxide @ polydopamine/poly (vinylidene fluoride) (PANI/rGO@PDA/PVDF) nanofiber piezoresistive sensor (PNPS) capable of versatile wearable biomonitoring. The PNPS was fabricated by integrating rGO sheets and PANI particles into a PDA-modified PVDF nanofiber network, where PDA was implemented to boost the interaction between the nanofiber networks and functional materials, PANI particles were deposited on a nanofiber substrate to construct electroactive nanofibers, and rGO sheets were utilized to interconnect nanofibers to strengthen in-plane charge carrier transport. Benefitting from the synergistic effect of multi-dimensional electroactive materials in piezoresistive membranes, the as-fabricated PNPS exhibits a high sensitivity of 13.43 kPa⁻¹ and a fast response time of 9 ms, which are significantly superior to those without an rGO sheet. Additionally, a wide pressure detection range from 0 to 30 kPa and great mechanical reliability over 12,000 cycles were attained. Furthermore, the as-prepared PNPS demonstrated the capability to detect radial arterial pulses, subtle limb motions, and diverse respiratory patterns, highlighting its potential for wearable biomonitoring and healthcare assessment. Full article

Lithium-ion batteries are restricted in development due to safety issues such as poor chemical stability and flammability of organic liquid electrolytes. Replacing liquid electrolytes with solid ones is crucial for improving battery safety and performance. This study aims to enhance the performance of polyethylene oxide (PEO)-based polymer via blending with poly(vinylidene fluoride-hexafluoropropylene) (P(VDF-HFP)). The experimental results showed that the addition of P(VDF-HFP) disrupted the crystalline regions of PEO by increasing the amorphous domains, thus improving lithium-ion migration capability. The electrolyte membrane with 30 wt% P(VDF-HFP) and 70 wt% PEO exhibited the highest ionic conductivity, widest electrochemical window, and enhanced thermal stability, as well as a high lithium-ion transference number (0.45). The cells assembled with this membrane electrolyte demonstrated an excellent rate of performance and cycling stability, retaining specific capacities of 122.39 mAh g⁻¹ after 200 cycles at 0.5C, and 112.77 mAh g⁻¹ after 200 cycles at 1C and 25 °C. The full cell assembled with LiFePO₄ as the positive electrode exhibits excellent rate performance and good cycling stability, indicating that prepared solid electrolytes have great potential applications in lithium batteries. Full article

Gel electrolytes (GEs) play a pivotal role in the advancement of lithium metal batteries by offering high energy density and enhanced rate capability. Nevertheless, their real-world application is hampered by relatively low ionic conductivity and significant interfacial resistance at room temperatures. In this work, we developed a gel electrolyte membrane (GEM) by embedding Zeolitic Imidazolate Framework-8 (ZIF-8) metal–organic frameworks (MOFs) material into a poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) matrix through UV curing. The composite membrane, with 4 wt% ZIF-8, exhibited an ionic conductivity of 1.17 × 10⁻³ S/cm, an electrochemical stability window of 4.7 V, and a lithium-ion transference number of 0.7. The test results indicate that the electrochemical performance of LFP//GEM//Li battery has an initial specific capacity of 168 mAh g⁻¹ at 0.1 C rate. At 1 C, the discharge capacity was 88 mAh g⁻¹, and at 2 C, it was 68 mAh g⁻¹. Enhanced ionic transport, improved electrochemical stability, and optimized lithium-ion migration collectively contributed to superior rate performance and prolonged cycle life. This study offers novel insights and methodological advances for next-generation lithium metal batteries technologies. Full article

Ultrafiltration is essential for wastewater treatment, but it faces challenges such as selectivity, control, and fouling reduction. Incorporating nanoparticles into membranes enhances retention, boosts permeability, and limits fouling, improving overall performance. This study explores the properties of PVDF/Ag-ZnO composite membranes, highlighting the influence of silver-doped zinc oxide nanoparticles on membrane structure, performance, and antimicrobial effect. The non-solvent-induced phase separation (NIPS) method successfully led to the preparation of composite membranes; this method used different doses of silver-doped zinc oxide (Ag-ZnO) nanoparticles with Poly(vinylidene fluoride) (PVDF). Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and water contact angle measurements were used to validate the influence of nanoparticles on the composite membrane (PVDF/Ag-ZnO) structure. Conversely, morphology (porosity, surface rigorosity), hydrophilicity, and permeability were analyzed through contact angle, image analysis, and flux measurement. In addition, the membranes were tested for antimicrobial activity against E. coli. Membrane performance shows that the incorporation of 20% w/w Ag-ZnO resulted in improved water permeability, which was about 2.73 times higher than that of a pure PVDF membrane (192.2 L·m⁻²·h⁻¹·bar⁻¹). The membrane porosity showed a linear increase with the number of NPs. The resultant asymmetric membrane was altered to increase the number of pores on the top surface by 61% and the cross-sectional pore surface by 663%. Furthermore, a high antibacterial activity of Ag-ZnO 20% was shown. Full article

This study explores the influence of various additives on the morphological, chemical, and thermal properties of poly(vinylidene fluoride) (PVDF) membranes prepared via the non-solvent induced phase separation (NIPS) technique. The use of a green solvent such as triethyl phosphate (TEP) was shown to be successful. A particular focus was dedicated to pore formers based on choline chloride–based deep eutectic solvents (DES) in combination with ethylene glycol and glycerol, i.e., ChCl/EG and ChCl/GLY, and its benchmark with traditional counterparts such as poly(ethylene glycol) (PEG) and glycerol (GLY). Comprehensive characterization was conducted using FESEM, FTIR, XRD, and DSC techniques to evaluate changes in membrane morphology, porosity, and crystallinity. PEG acted as a pore-forming agent, transitioning the internal structure from spherulitic to sponge-like with consistent pore sizes, while GLY produced a nodular morphology at higher concentrations due to increased dope solution viscosity. DES induced significant shifts in crystalline phase composition, decreasing α-phase fractions and promoting β-phase formation at higher concentrations. While the overall porosity remained unaffected by the addition of GLY or PEG, it was dependent on the DES concentration in the dope at lower values than those obtained by GLY and PEG. Membrane pore size with ChCl/GLY was lower than with ChCl/EG and GLY. All membranes showed performance at the hydrophobic regime. The findings demonstrate that ChCl/EG and ChCl/GLY can tailor the structural and thermal properties of TEP-driven PVDF membranes, providing a green and versatile approach to customize the membrane properties for specific applications. Full article

Bone tissue is intrinsically electroactive, and electrical signaling is one of its key regulatory mechanisms. The electroactive poly (vinylidene fluoride trifluoroethylene) (PVTF), due to its piezoelectricity, can provide electrical stimulation to cells, regulating their proliferation and osteogenic differentiation. Collagen I (COL) is the main organic component of bone and is involved in various physiological processes of bone. A crucial question that remains to be explored is whether electroactive materials can meet the requirements for GBR membranes and what synergistic effects electrical signals and collagen’s biochemical signals might have on cellular behavior. In this study, PVTF/COL composite films were prepared using polydopamine (PDA). It was found that collagen modification could increase the surface Kelvin potential of PVTF from −5.07 V to 2.22 V, reduce the WCA from 98.9° to 33.2°, and maintain the tensile strength of PVTF at 24.94 MPa. Additionally, the composite film significantly promoted the adhesion and proliferation of bone marrow stem cells (BMSCs), and the ALP activity on PPC3 films after 7 days was 5.6 times higher than that on P films. This study presents a novel and effective approach for surface modification of PVTF and explores its potential applications in GBR. Full article

Flexible and wearable electronics often rely on piezoelectric materials, and Poly(vinylidene fluoride-trifluoroethylene) (P(VDF-TrFE)) membranes are popular for this application. However, their electromechanical performance is limited due to a relatively low piezoelectric coefficient. To address this, this study investigates the incorporation of zinc oxide (ZnO) nanorods (NRs) into a P(VDF-TrFE) nanofiber membrane matrix. ZnO NRs were synthesized and doped into well-aligned P(VDF-TrFE) nanofibers using electrospinning with a high-speed rotating drum. The impact of ZnO NRs’ mass fraction on the piezoelectric properties of the membranes was evaluated. Results show that a maximum piezoelectric coefficient ($d_{33}$) of −62.4 pC/N, 9.5 times higher than neat P(VDF-TrFE), was achieved. These enhanced membranes demonstrated excellent performance in finger-tapping and bending detection, making them promising for large-scale flexible sensor applications in wearable electronics. This approach offers a simple and effective route to improve the performance of piezoelectric materials in flexible devices. Full article

The morphology of Poly (vinylidene fluoride) (PVDF) membranes prepared via the nonsolvent-induced phase separation (NIPS) method was modulated by altering the dope solution with citric acid (CA) and titanium dioxide nanoparticles (nano-TiO₂) to optimize the β-phase content. Three series of dope solutions were prepared in dimethyl acetamide (DMAc): (i) TONx series contained 0.0–10% citric acid, (ii) Mx series contained 0.0–0.4% nano-TiO₂, and (iii) TAx series contained 5% CA and 0.0–0.40% nano-TiO₂. A field emission scanning electron microscopy (FESEM) study revealed that CA enhances pore opening, and nano-TiO₂ transforms the sponge-like uneven porous structures into a compact, relatively regular honeycomb structure in the PVDF membranes. The combined effect of CA and nano-TiO₂ in the dope solution made the channels and chambers of the membrane well organized, and the walls of the channels transformed from solid fibrils to cross-woven nanofiber-like entities. Porosity initially peaked at 84% in the TAx series, gradually decreasing to 72% with increasing nano-TiO₂ concentrations. X-ray diffraction (XRD), Fourier-Transformed Infrared Spectroscopy (FTIR), and Differential Scanning Calorimetry (DSC) revealed the presence of a combined relative amount of the β- and γ-polymorphs of 84% in a neat PVDF membrane, 88% in an Mx, and 96% in a TAx series membrane, with the β-PVDF constituting nearly the entire portion of the combined polymorphs. The presence of 96% electroactive polymorph content in the PVDF membrane is noteworthy, highlighting its potential biomedical and industrial applications. Full article

Functional membranes with waterproof, breathable, and thermal regulation capabilities are increasingly sought after across various industries. However, developing such functional membranes commonly involves complex multi-step preparation processes. Herein, we introduced perfluorodecyltriethoxysilane (FAS) into the poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) solution for one-step electrospinning, successfully fabricating membranes that combine these properties. The hydrophobicity of the PVDF-HFP/FAS membrane was greatly improved with the water contact angle increased from 120.6° to 142.9° and the solar reflectance rising from 72% to 92% due to the presence of fluorocarbon segments. The synergistic effect of enhanced hydrophobicity, small pore size, and elevated solar reflectivity resulted in robust water resistance (62 kPa), excellent water vapor transmission rate (12.4 kg m⁻² d⁻¹), and superior cooling performance (6.4 °C lower than commercial cotton fabrics). These findings suggest that the proposed PVDF-HFP/FAS membranes, characterized by desired multifunction characteristics and scalable production, hold great potential for application in diverse strategic fields. Full article

Immobilizing different enzymes on membranes can result in biocatalytic active membranes with a self-cleaning capacity toward a complex mixture of foulants. The membrane modification can reduce fouling and enhance filtration performance. Protease, lipase, and amylase were immobilized on poly(vinylidene fluoride) (PVDF) microfiltration membranes using a polydopamine coating in a one-step method. The concentrations of polydopamine precursor and enzymes were optimized during the immobilization. The higher hydrolytic activities were obtained using 0.2 mg/mL of dopamine hydrochloride and 4 mg/mL of enzymes: 0.90 mg_starch/min·cm² for amylase, 10.16 nmol_tyrosine/min·cm² for protease, and 20.48 µmol_{p-nitrophenol}/min·cm² for lipase. Filtration tests using a protein, lipid, and carbohydrate mixture showed that the modified membrane retained 41%, 29%, and 28% of its initial water permeance (1808 ± 39 L/m²·h·bar) after three consecutive filtration cycles, respectively. In contrast, the pristine membrane (initial water permeance of 2016 ± 40 L/m²·h·bar) retained only 23%, 12%, and 8%. Filtrations of milk powder solution were also performed to simulate dairy industry wastewater: the modified membrane maintained 28%, 26%, and 26% of its initial water permeance after three consecutive filtration cycles, respectively, and the pristine membrane retained 34%, 21%, and 7%. The modified membrane showed increased fouling resistance against a mixture of foulants and presented a similar water permeance after three cycles of simulated dairy wastewater filtration. Membrane fouling is reduced by the immobilized enzymes through two mechanisms: increased membrane hydrophilicity (evidenced by the reduced water contact angle after modification) and the enzymatic hydrolysis of foulants as they accumulate on the membrane surface. Full article

Graphene oxide-silver poly(vinylidene fluoride) membranes (PVDF@GO-Ag) were successfully synthesized by the electrospinning method, which exhibited a high catalytic activity using the hydrogenation of 4-nitrophenol (4-NP) as a model reaction in a batch reaction study. The hybrid membranes doped with 1 wt% GO and 2 wt% Ag (PVDF-1-2) exhibited the most desired performance for the catalytic reduction of 4-NP. Importantly, PVDF-1-2 exhibited excellent cycling stability in 10 catalytic cycle tests and was highly amenable to separation. This property effectively addresses the significant challenges associated with the practical application of nanocatalysts. Furthermore, density-functional theory (DFT) calculations have demonstrated that the GO-Ag nanocomposites exhibit the strongest adsorption capacity for 4-NP⁻ when a specific ratio of GO and Ag is achieved, accompanied by the loading of Ag nanoclusters onto GO. Additionally, the study demonstrated that an increase in temperature significantly accelerated the reaction rate, in line with the van’t Hoff rule. This study provides an effective and environmentally friendly solution for the treatment of 4-NP in wastewater. Full article

Porous silicon dioxide (SiO₂)/poly(vinylidene fluoride) (PVdF), SiO₂/PVdF, and fibrous composite membranes were prepared by electrospinning a blend solution of a SiO₂ sol–gel/PVdF. The nanofibers of the SiO₂/PVdF (3/7 wt. ratio) blend comprised skin and nanofibrillar structures which were obtained from the SiO₂ component. The thickness of the SiO₂ skin layer comprising a thin skin layer could be readily tuned depending on the weight proportions of SiO₂ and PVdF. The composite membrane exhibited a low thermal shrinkage of ~3% for 2 h at 200 °C. In the prototype cell comprising the composite membrane, the alternating current impedance increased rapidly at ~225 °C, and the open-circuit voltage steeply decreased at ~170 °C, almost becoming 0 V at ~180 °C. After being exposed at temperatures of >270 °C, its three-dimensional network structure was maintained without the closure of the pore structure by a melt-down of the membrane. Full article