Search Results (971)

Polymeric vesicles, characterized by enhanced colloidal stability, excellent mechanical properties, controllable surface functionality, and adjustable membrane thickness, are extremely useful in nano- and bio-technology for potential applications as nanosized carriers for drugs and enzymes. However, a few preparative steps are necessary to achieve a unilamellar vesicle with a narrow size distribution. Herein, we report the spontaneous formation of unilamellar polymeric vesicles with nanometer sizes (<50 nm), fabricated by simply mixing diblock copolymers (P(EO-AGE)(2K-2K) and P(EO-AGE)(0.75K-2K)) with differing hydrophilic mass fractions in aqueous solutions. Depending on the mixing ratio of block copolymers and the temperature, the block copolymer mixtures self-assemble into various nanostructures, such as spherical and cylindrical micelles, or vesicles. The self-assembled structures of the block copolymer mixtures were characterized by small-angle neutron scattering, resulting in a phase diagram drawn as a function of temperature and the mixing condition. Notably, the critical temperature for the micelle-to-vesicle phase transition can be easily controlled by altering the mixing conditions; it decreases with an increase in the concentration of one of the block copolymers. Full article

This study investigates TNM-type titanium aluminide alloys, representing the third generation of β-stabilized γ-TiAl heat-resistant materials. The aim of this work is to study the combustion characteristics and to produce compact materials via the free SHS compaction method from initial powder reagents taken in the following ratio (wt%): 51.85Ti–43Al–4Nb–1Mo–0.15B, as well as to determine the effect of high-temperature isothermal annealing at 1000 °C on the structure and properties of the obtained materials. Using free SHS compression (self-propagating high-temperature synthesis), we synthesized compact materials from a 51.85Ti–43Al–4Nb–1Mo–0.15B (wt%) powder blend. Key combustion parameters were optimized to maximize the synthesis temperature, employing a chemical ignition system. The as-fabricated materials exhibit a layered macrostructure with wavy interfaces, aligned parallel to material flow during compression. Post-synthesis isothermal annealing at 1000 °C for 3 h promoted further phase transformations, enhancing mechanical properties including microhardness (up to 7.4 GPa), Young’s modulus (up to 200 GPa) and elastic recovery (up to 31.8%). X-ray powder diffraction, SEM, and EDS analyses confirmed solid-state diffusion as the primary mechanism for element interaction during synthesis and annealing. The developed materials show promise as PVD targets for depositing heat-resistant coatings. Full article

This study explores the challenge of using anthocyanin-rich natural deep eutectic solvent (NADES) extracts to produce electrospun nanofibers for biodegradable freshness indicators. Red cabbage was extracted with two choline chloride-based NADESs (with citric or lactic acid), modified with 10–50% ethanol to lower viscosity, and compared with a standard 50% ethanol-water solvent. The citric acid NADES with 30% ethanol gave the highest anthocyanin yield (approx. 0.312 mg/mL, more than 20 times higher than the ethanol extract at approx. 0.014 mg/mL). For fiber fabrication, a polymer carrier blend of poly(ethylene oxide) (PEO) and sodium alginate (Alg) was employed, known to form hydrogen-bonded networks that promote chain entanglement and facilitate electrospinning. Despite this, the NADES extracts could not be electrospun into nanofibers, while the ethanol extract produced continuous, smooth fibers with diameters of approximately 100 nm. This highlights a clear trade-off; NADESs improve anthocyanin recovery, but their high viscosity and low volatility prevent fiber formation under standard electrospinning conditions. To leverage the benefits of NADES extracts, future work could focus on hybrid systems, such as multilayer films, core-shell fibers, or microcapsules, where the extracts are stabilized without relying solely on direct electrospinning. In storage tests, ethanol-extract nanofibers acted as effective pH-responsive indicators, showing visible color change from day 4 of meat storage. At the same time, alginate films with NADES extract remained unchanged after 12 days. These results highlight the importance of striking a balance between chemical stability and sensing sensitivity when designing anthocyanin-based smart packaging. Full article

Healthcare-associated infections (HAIs) pose a significant risk in clinical settings by extending hospitalization times and increasing healthcare costs. This study aimed to evaluate the effectiveness of gaseous ozone, generated by an automatic rotary dispenser, in disinfecting hospital fabrics contaminated with common HAI-related pathogens. The antimicrobial efficacy of ozone was tested on cotton, polyester, and blended fabrics artificially contaminated with Staphylococcus aureus, Escherichia coli, and Candida albicans. The fabrics were exposed to ozone treatment cycles of 25 and 45 min. Additional tests were conducted on layered fabrics to assess ozone penetration into folds and seams. A 25 min ozone exposure significantly reduced the microbial load on all tested fabrics. A 45 min cycle resulted in an almost complete elimination of the tested pathogens. Ozone also effectively disinfected inner fabric layers, indicating its ability to reach areas typically resistant to conventional cleaning methods. Gaseous ozone demonstrates high efficacy as a disinfectant for hospital textiles, offering thorough decontamination across various materials and fabric structures. This technology represents a sustainable, residue-free alternative to traditional disinfection methods and promises to reduce the transmission of HAIs in healthcare environments. Full article

The development of a straightforward strategy for preparing organic fluorescent materials, fine-tuning white-light emission, and subsequently constructing white light-emitting diodes (LEDs) is of great significance. Herein, we report on the modulation of white-light emission and the fabrication of white LEDs using polyhedral oligomeric silsesquioxane (POSS)-based fluorescent hybrid porous polymers (HPPs) through simple physical blending. Two HPPs, namely HPP-1 and HPP-2, which emit blue and red light, respectively, were synthesized via the efficient Heck reactions of octavinylsilsesquioxane with 4,4′-dibromobiphenyl and 1,3,6,8-tetrabromopyrene. By physically doping of HPP-1 and HPP-2 in variable ratios in solvent suspensions, it was discovered that white-light emission is significantly influenced by the concentrations of the materials and the excitation wavelength. Similar findings were also observed in the solid-state physical doping. An ideal white light emission with a CIE coordinate of (0.33, 0.33) can be achieved when excited at 380 nm with a mass ratio of HPP-1 to HPP-2 of 1:2. Finally, the two HPPs were dispersed in polysiloxane matrices, and a white LED with a CIE coordinate of (0.42, 0.36) was obtained. The LED exhibited a color rendering index of up to 90 and a correlated color temperature of 2858 K, realizing warm white light emission. This simple and convenient white-light regulation strategy holds great promise for application in the development of novel white LEDs based on organic fluorescent porous materials. Full article

Veneer-based wood composites are widely used for interior applications, yet their high flammability and smoke emission significantly limit their safe use in buildings. In this study, a multifunctional flame-retardant polyethylene adhesive film was developed via melt blending and hot pressing of a mixture of amino trimethylene phosphonic acid (ATMP), hydroxyethylidene diphosphonic acid (HDEP), melamine (MEL), and sodium alginate (SA). This film was laminated onto veneers to fabricate flame-retardant decorative plywood. Simultaneously, wood scrimber units for structural applications were prepared by impregnating wood with a flame-retardant system consisting of sodium silicate (Ss) and sodium tetraborate (St). These treated components were integrated to form a flame-retardant wood scrimber/plywood composite (AHM-S), with the wood scrimber as the core layer and the treated plywood as surface layers. Compared to the control, the AHM-S composite showed a 44.1% reduction in the second peak heat release rate (pk-HRR2), a 22.6% decrease in total heat release (THR), and a 12.7% reduction in maximum flame spread distance (MD_300°C). Moreover, the time to reach 275 °C on the unexposed side (T_275°C) was extended by 90.2%. These improvements are attributed to the synergistic flame-retardant effects of the surface film and impregnated core, which jointly suppress flame spread and delay thermal degradation. The composite demonstrates promising fire safety and mechanical performance for engineered wood applications. Full article

In recent years, paper-based humidity sensors have emerged as a highly promising technology for humidity detection. In this work, a polymerizable deep eutectic solvent (PDES) was prepared via a one-step blending method, which was applied to modify filter paper. The modification process did not alter the overall structure of the paper cellulose but rather targeted only its internal cellulose channels, thereby minimizing any impact on the paper’s original moisture-independent properties. The filter paper functioned both as the substrate and the humidity-sensing material in the fabricated sensor. The finger-like electrodes were designed using AutoCAD 2018 software and then printed onto the modified paper using screen-printing technology to fabricate the humidity sensor. Different saturated salt solutions were used to simulate corresponding humidity environments and evaluate the humidity performance of sensors. Compared with that of the blank paper-based humidity sensor, the sensitivity of the sensor modified by the PDES was significantly greater, and the recovery time was greatly shorter. Specifically, the sensitivity increased from 1.34 to 10.36 at 54% RH and from 166.24 to 519.2 at 98% RH. Additionally, the sensor response time was reduced from 728 s to 137 s. PDES modification significantly improved the moisture-sensitive characteristics and detection performance of the sensor. Full article

Bio-based nanofibers are gaining increasing attention in nanotechnology owing to their high surface area, interconnected porosity, and capacity to incorporate bioactive compounds. Among natural polymers, gelatin is particularly attractive because of its abundance, low cost, biodegradability, and versatile physicochemical properties. When processed by electrospinning, gelatin combines its amphiphilic nature with the structural advantages of nanofibers, enabling efficient interactions with a wide range of molecules. Nevertheless, pure gelatin nanofibers have drawbacks, such as poor mechanical strength and high-water solubility. To address these limitations, strategies including polymer blending, chemical and physical crosslinking, and multilayer biomaterials have been developed, resulting in improved stability, functionality, and application-specific performance. Therefore, this review summarizes recent advances in the fabrication and functionalization of gelatin nanofibers, highlighting how processing parameters and gelatin source influence electrospinning outcomes and fiber properties. Key applications are also discussed, with emphasis on biomedical, food, environmental, and biosensing. Therefore, gelatin nanofibers represent a sustainable and versatile biomaterial with high potential for advanced technological applications. Full article

The purpose of this study was to obtain a holistic view of mechanically recycled cotton from denim fabrics and the repurposing and recycling methods for similar fibres. A pre-consumer denim and three types of post-consumer denims were shredded into new fibres, which were characterised with single-fibre tensile testing, SEM imaging and DSC analysis. The opened cotton fibres were then blended with primary cotton with varying ratios and spun into yarns of 40 tex with a ring spinning machine. A ratio of 75/25 of recycled fibres to virgin fibres was obtained, with promising tensile strength results. Further, the yarns were knitted into single jersey fabrics, and abrasion testing was performed to evaluate their wearing out. Best abrasion resistance was obtained for knits consisting of 100% virgin cotton fibres and the knits consisting of a blend of pre-consumer and virgin fibres. The results suggest the yarns made with mechanically opened fibres are suitable for single jersey knits. SEM and DSC confirm the input of mechanical recycling defines the output. Moreover, the SEM pictures indicate there is little to no damage to single fibres caused by mechanical shredding, causing no further barriers for secondary use as raw materials. Full article

Novel blend membranes containing S-PVA and PEBAX 1657 at a blend ratio of 8:2 were doped with varying amounts of titanium dioxide phosphate (TiO₂PO₄) as a nanoparticle filler at concentrations of 0, 3, 5, and 7 wt%. The membranes were fabricated using the solution-casting technique. The effect of the TiO₂PO₄ nanofiller on the polymer matrix was thoroughly investigated. Our aim was to investigate how the incorporation of TiO₂PO₄ nanofillers into non-fluorinated SPP-based membranes affects their structural, physicochemical, and electrochemical properties for application in fuel cells. Crystallinity of the samples was checked by means of X-ray diffraction (XRD), while FTIR was used to investigate the contact between the nanofiller and the polymers. The good compatibility resulted in strong interactions between the constituents and led to increased crystallinity of the membrane as well. Furthermore, SEM images confirmed the uniform distribution of the nanofiller. These structural features led to good thermal stability, as evidenced by thermogravimetric analysis (TGA), and good mechanical strength, as proved by tensile tests. Among the samples investigated, the highest water uptake of 51.70% was achieved on the composite membrane containing 3 wt% TiO₂PO₄, which also showed the highest ion exchange capacity at room temperature, reaching 1.13 meq/g. In line with these properties, among the synthesized membranes, the membrane labeled SPP 3% TiO₂PO₄ has the highest current density and power density, with values of 175.5 mA/cm² and 61.52 mW/cm², respectively. Full article

Background/Objectives: Recent advancements in biomaterials aimed at closely mimicking natural biological tissues hold great promise for hard tissue regeneration and controlled drug release due to their superior physical, chemical, and biological properties. This study aimed to develop multi-ion doped calcium hydroxyapatite (HAp) scaffolds with chitosan-based coatings for localized drug delivery, incorporating a novel hydrazone compound with potential anticancer activity. Methods: HAp powders doped with magnesium (Mg²⁺), strontium (Sr²⁺), and varying fluoride (F⁻) contents (0–2 mol.%) were synthesized via a hydrothermal method. Scaffolds were fabricated using the sponge replica technique and subsequently coated with chitosan or a chitosan–hydrazone blend. Dopant incorporation was confirmed by electron dispersive X-ray spectroscopy (EDS). Phase composition and morphology were analyzed via X-ray diffraction (XRD) and scanning electron microscopy (SEM). Mechanical properties, bioactivity, cytotoxicity, and hydrazone release profiles were systematically evaluated. Results: EDS confirmed successful incorporation of Mg²⁺ and Sr²⁺ in all powders, while F⁻ was detected only in powders with 1 and 2 mol.% fluoride. XRD and SEM revealed the phase composition and scaffold microstructure. Chitosan coatings significantly improved scaffold compressive strength and reduced degradation rate, indicating enhanced stability in biological environments. The coated scaffolds supported MRC-5 fibroblast viability. The hydrazone compound exhibited dose-dependent antitumor cytotoxicity comparable to cisplatin and showed sustained release from scaffolds for up to 15 days. Conclusions: The combination of multi-ion doped HAp scaffolds and chitosan–hydrazone coatings provides a promising platform for bone tissue engineering and localized cancer therapy, demonstrating both mechanical stability and controlled, sustained drug release. Full article

The development of thin-film organic solar cells (TFOSCs) is pivotal for advancing sustainable energy technologies because of their potential for low-cost, lightweight, and flexible photovoltaic applications. In this study, silver-doped copper sulfide (CuS/Ag) metal nanoparticles (MNPs) were successfully synthesized via a wet chemical method. These CuS/Ag MNPs were incorporated at varying concentrations into a poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) blend, serving as the active layer to enhance the photovoltaic performance of the TFOSCs. The fabricated TFOSC devices were systematically evaluated based on the optical, electrical, and morphological characteristics of the active layer. By varying the concentration of CuS/Ag MNPs, the influence of nanoparticle doping on photocurrent generation was investigated. The device incorporating 1% CuS/Ag MNPs exhibited the highest power conversion efficiency (PCE) of 5.28%, significantly outperforming the pristine reference device, which achieved a PCE of 2.53%. This enhancement is attributed to the localized surface plasmon resonance (LSPR), which augments charge transport and increases optical absorption. The CuS/Ag MNPs were characterized using ultraviolet–visible (UV-Vis) absorption spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and energy-dispersive dispersion (EDX) analysis. These findings underscore the potential of CuS/Ag MNPs in revolutionizing TFOSCs, paving the way for more efficient and sustainable solar energy solutions. Full article

A novel approach was developed in this work in which composite nanofiltration (NF) membranes were directly and efficiently fabricated with control of the membrane pore structure and surface morphology. The fabrication of mesoporous silicon-modified polysulfone blend membranes is achieved via a phase inversion method. The structural morphology, surface functional group analysis, elemental analysis, hydrophilicity, chargeability, and nitrogen pollutant (ammonia nitrogen, nitrate nitrogen, total nitrogen) rejection properties of the modified membranes were found to be dependent on the amount of mesoporous silicon incorporated. The combination of the mesoporous silicon framework layer can not only effectively improve the surface structure of the modified membrane with a narrow pore size distribution but also increase the rejection of nitrogen pollutants compared with pure NF membranes. The mesoporous material interlayer can absorb and store the aqueous amino solution to facilitate the subsequent interfacial polymerization as well as induce changes in the pore radius and surface structure. Compared with pure NF composite membranes, the modified blend membranes exhibit increased water permeation flux as high as 29.09 L m⁻² h⁻¹ at 0.2 MPa. The results show that the optimum doping amount of mesoporous silicon is in the range of 0.5–1.0%. Characterization studies demonstrated that the addition of mesoporous silicon leads to a decreased membrane pore size. Then the retention of nitrogen pollutants was enhanced because of a combination of hydrophilicity enhancement from the carboxylic and hydroxyl functional groups present in their surfaces leading to electrostatic repulsion between functional groups present in the membranes and the nitrogen pollutant molecules. Full article

This study aims to address the poor extensibility, brittleness, and limited hydration stability of pure sodium alginate (SA) hydrogels, which hinder their use in flexible, skin-adherent applications such as facial masks, by developing bio-based composites incorporating five representative functional additives: xanthan gum, guar gum, hydroxyethyl cellulose (HEC), poly(ethylene glycol)-240/hexamethylene diisocyanate copolymer bis-decyl tetradeceth-20 ether (GT-700), and Laponite^® XLG. Composite hydrogels were prepared by blending 1.5 wt% SA with 0.3 wt% of each additive in aqueous humectant solution, followed by ionic crosslinking using 3% (w/w) CaCl₂ solution. Physicochemical characterization included rotational viscometry, uniaxial tensile testing, ATR-FTIR spectroscopy, swelling ratio analysis, and pH measurement. Among them, the SA/XLG composite exhibited the most favorable performance, showing the highest viscosity, shear-thickening behavior, and markedly enhanced extensibility with an elongation at break of 14.8% (compared to 2.5% for neat SA). It also demonstrated a mean swelling ratio of 0.24 g/g and complete dissolution in water within one year. ATR-FTIR confirmed distinct non-covalent interactions between SA and XLG without covalent modification. The hydrogel also demonstrated excellent conformability to complex 3D surfaces, consistent hydration retention under centrifugal stress (+23.6% mass gain), and complete biodegradability in aqueous environments. Although its moderately alkaline pH (8.96) may require buffering for dermatological compatibility, its mechanical resilience and environmental responsiveness support its application as a sustainable, single-use skin-contact material. Notably, the SA/XLG composite hydrogel demonstrated compatibility with personalized fabrication strategies integrating 3D scanning and additive manufacturing, wherein facial topography is digitized and transformed into anatomically matched molds—highlighting its potential for customized cosmetic and biomedical applications. Full article

Hybrid organic–inorganic materials incorporating high-Z nanocompounds represent an emerging area of research with high, cost-effective potential for radiation detection applications, owing to their ability to enable unprecedented architectures and functional devices. Herein, we introduce a new hybrid system composed of tungstate nanoparticles (SrWO₄ or CdWO₄) blended with P3HT:PCBM, engineered for direct X-ray detection without the need for external bias. The nanocrystalline tungstates were synthesized through a hydrothermal route. X-ray diffraction and scanning electron microscopy were employed to characterize the nanoparticle structure and morphology, respectively. Incorporation of high-Z tungstate nanoparticles was found to substantially enhance detector sensitivity within specific energy ranges, with performance tunable by varying the tungstate composition. The use of the fabricated detectors was demonstrated for both spectroscopic and imaging applications. Full article