Search Results (4,590)

The food packaging industry requires sustainable solutions to reduce plastic waste and replace synthetic additives. This study addresses the need for scalable methods to transform conventional polyethylene terephthalate (PET) packaging into active food preservation systems using natural biocides. Commercial PET packaging was surface-activated using industrial-scale corona treatment, followed by coating with natural biocides—carvacrol (CV) and trans-cinnamaldehyde (tCN). The resulting active packaging materials (PET-CV and PET-tCN) were characterized using XRD, FTIR, SEM, AFM, and desorption kinetics. Packaging properties including mechanical strength, oxygen barrier, antioxidant (DPPH), and antibacterial activity (against S. aureus and E. coli) were evaluated. Real-food preservation tests were conducted using fresh minced pork (4 °C, 6 days) and table olives (23 °C, 21 days), monitoring microbiological (TVC), colorimetric (CIE L*a*b*), and pH changes. Corona treatment successfully anchored both biocides through physical adsorption, with tCN exhibiting stronger surface interaction (desorption energy: 128.0 kJ/mol). Both coatings significantly improved oxygen barrier properties (61% reduction for PET-CV, 80% for PET-tCN). PET-tCN demonstrated superior antibacterial activity (inhibition zones: 15.0 mm against E. coli). In pork preservation, PET-tCN achieved a 2-log reduction in TVC, maintained meat redness (a*: 12.80 vs. 5.10 for control), and stabilized pH. For olives, PET-tCN reduced TVC by 2.35 log cycles and preserved green color. This corona-assisted coating approach, demonstrated here at laboratory scale, successfully transforms inert PET into multi-functional active packaging with potent antimicrobial, antioxidant, and barrier properties, significantly extending food shelf-life and offering a sustainable solution for reducing food waste. Full article

Molecularly imprinted polymers (MIPs) are widely employed for selective adsorption of target molecules in sensing and separation applications. The architecture of MIP films can influence adsorption behavior, interfacial stability, and reusability, yet systematic investigations of these effects are limited. This study aimed to evaluate how different polypyrrole (PPy) MIP film architectures affect the adsorption, stability, and regeneration characteristics of geraniol-imprinted layers on gold electrodes. Geraniol-imprinted and non-imprinted PPy films were electropolymerized onto quartz crystal microbalance (QCM) substrates. Two film architectures were compared: (i) a single-layer geraniol-imprinted PPy film, and (ii) a double-layer film consisting of a non-imprinted PPy underlayer followed by a geraniol-imprinted layer. Film characterization was performed using cyclic voltammetry (CV) and electrochemical quartz crystal microbalance (EQCM) measurements. Adsorption–desorption cycles were conducted to assess mass uptake, signal stability, and regeneration performance. EQCM analysis revealed that the double-layer architecture exhibited enhanced frequency signal stability during repeated adsorption–desorption cycles compared to single-layer films, suggesting a stabilizing effect of the underlying non-imprinted PPy layer at the electrode interface. Geraniol-imprinted films demonstrated significantly higher mass uptake than non-imprinted controls, confirming the sensitivity provided by molecular imprinting. Single-layer films showed more variability in signal response and less consistent regeneration performance. The architecture of MIP films significantly affects adsorption behavior, stability, and regeneration on electrode surfaces. Incorporating a non-imprinted PPy underlayer can improve signal reproducibility and enhance the robustness of MIP-based sensing interfaces. These findings provide guidance for the rational design of MIP coatings for electrochemical sensors and QCM-active platforms. Full article

To meet the requirements of flexibility and high performance for energy storage devices in flexible wearable electronic equipment, the MnO₂/acetylene black composite flexible cathodes is fabricated via 3D printing technology and the aqueous manganese-based zinc-ion flexible batteries are assembled. Based on bending and torsion mechanical tests, and the electrochemical tests, the optimal 3D printing electrode structure was determined. The micromorphology of the electrode after mechanical tests shows that when the printed lines of the upper and lower layers form a 30° angle, the electrode sheet exhibits the least damage. Electrochemical tests indicated that it had an ohmic resistance of 2.052 Ω, an interfacial charge transfer resistance of 141.1 Ω, a specific capacity of 103 mAh/g at 50 mA/g, and a specific capacity of 65 mAh/g at 500 mA/g. Compared with traditional coated electrodes, the 3D-printed electrode showed significantly improved diffusion coefficient, conductivity, and cycle stability. The assembled 3D-printed flexible battery could stably power a 1.5 V LED bulb under flat, bent, and twisted states. It provides a feasible solution for the development of high-performance flexible energy storage devices. Full article

In this paper, an Artificial Neural Network (ANN) is built to predict the performance of intumescent coatings subjected to the ISO 384 fire curve. The performance metric is called the Retention Loss Onset Time (RLOT) in the structural steel. The network receives the steel and coating thicknesses as input and provides RLOT as the performance of any intumescent coating in a fire accident with substantial accuracy. The required data for obtaining the model is provided by revisiting the recent attempts in this field, which include hybrid numerical and experimental methods. It is found that the trapped gas fraction parameter and empirical expansion ratio substantially affect the accuracy of predictive modelling. Therefore, a new, comprehensive dynamic model that numerically simulates the bubble expansion process has been developed. This novel method directly determines the expansion ratio of the thermal conductivity model. The Eurocode is then used with multi-layer models to predict the steel temperature profile for a 1 h duration ISO fire. The accuracy is improved by modelling the temperatures and thermal resistances at the centre of each divided layer. The effects of different coatings and steel thicknesses are also investigated to provide the required data. The results are verified and validated by comparing them with the recent numerical and empirical results available in the literature. Full article

Ionic polymer–metal composites consist of an ion-conducting polymer–gel membrane sandwiched between two flexible electrodes, representing a class of soft electroactive materials capable of large deformation under low voltage. The gel membrane, swollen with solvent, facilitates ion migration under an electric field, enabling actuation. Tailoring the interfacial architecture between the electrode and the polymer–gel membrane is pivotal for advancing high-performance IPMC actuators. This study presents a comparative investigation of three core–shell nanocomposite electrodes, fabricated via in situ polymerization, for IPMC applications. Among these, the polyaniline-coated multi-walled carbon nanotube composite exhibits a deliberately designed hierarchical structure, with a specific surface area of 32.345 m²·g⁻¹ and a conductive doped polyaniline shell, as confirmed through XPS analysis. This optimized interface enables superior charge storage and transport, endowing the corresponding electrode with a specific capacitance of 40.28 mF·cm⁻² at 100 mV·s⁻¹—3.2 times greater than that of conventional silver-based electrodes—along with a reduced sheet resistance. When integrated with a Nafion ion–gel membrane, the PANI@MWCNT electrode achieves a 67% increase in force density and a larger displacement output compared to standard devices, directly correlated with its enhanced electrical and electrochemical properties. This work highlights the critical role of core–shell interfacial engineering in governing electromechanical performance at the electrode–gel interface and offers a practical design strategy for developing high-performance, cost-effective IPMC actuators for soft robotics, flexible electronics, and related applications. Full article

A novel sensitive and selective electrochemiluminescence (ECL) sensor using nitrogen-doped graphyne as the platform was proposed for kanamycin (KAN) detection. First, nitrogen-doped graphyne nanomaterial (1N-GY) with high conductivity was synthesized using a high-energy ball milling method. Compared with ordinary graphyne, the addition of nitrogen atoms can improve the conductivity of the material and reduce the electronic migration energy barrier. Then it was used as a substrate material of the ECL sensor, not only increasing the conductivity of the biosensor but also improving the sensitivity of the ECL sensor by providing more immobilization space for the luminescent probe of Nafion-coated mesoporous silica adsorbed Ru(bpy)₃²⁺ (mSiO₂@Nafion@Ru(bpy)₃²⁺). On this basis, mSiO₂@Nafion@Ru(bpy)₃²⁺ functionalized DNA probes were used as luminescent and capture probes to specifically recognize different concentrations of KAN to produce ECL signals. Under optimal conditions, the proposed ECL sensor exhibited good linearity (10⁻¹²–10⁻⁶ M KAN) and a low detection limit of 1.08 pM. The prepared biosensor with good stability and selectivity successfully detected KAN in honey and milk samples, with spiked recovery rates ranging from 98% to 111.79%. This method not only expands the application of 1N-GY as a novel graphitic material in ECL biosensors but also provides an effective way to check antibiotics in dairy products. Full article

With the rapid development of electrified railways in high-altitude regions, section insulators in catenary systems frequently experience gap breakdown and surface flashover under low atmospheric pressure conditions, posing serious threats to safe train operation. This paper investigates the discharge mechanisms of section insulators in high-altitude environments and conducts research on discharge characteristics under extremely non-uniform electric fields, along with structural optimization. First, the physical mechanisms of gap discharge and surface flashover in section insulators are analyzed. A three-dimensional electric field simulation model of the section insulator is established, and numerical analysis is performed to reveal the electric field distribution characteristics. The results indicate that the electric field is predominantly concentrated at the junction between metal electrodes and insulators, as well as at the tip of the arcing horn. The local maximum field strength reaches 3.84 × 10⁵ V/m, exceeding the corona inception field strength of air, which readily induces discharge. Subsequently, power frequency and lightning impulse discharge tests are conducted in both plain region and regions at an altitude of 4300 m. The results show that under high-altitude conditions, the power frequency breakdown voltage decreases by 28%, and the 50% lightning impulse breakdown voltage decreases by 42%. The discharge voltages under standard atmospheric conditions are obtained through correction. Finally, optimization schemes involving arcing horn structural modification and surface coating application are proposed. Adjusting the arcing horn angle to 55° and adding a grading ring structure with a radius of 70 mm reduces the local maximum field strength by 26%. After applying an RTV insulating coating, the field strength at the junction decreases by 35.9%, effectively enhancing the insulation performance of section insulators in high-altitude regions. Full article

Graphene and graphene oxide are potential anti-corrosion materials. In this study, epoxy resin/graphene and epoxy resin/graphene oxide composite coatings were succeed prepared. Hydrogen evolution and electrochemical experiments were conducted to determine key parameters—including hydrogen evolution rate, hydrogen evolution volume, corrosion current density, and corrosion potential—of the designed composites in a 3.5 wt.% NaCl solution. The sample with the highest graphene oxide content was 0.8295 μA/cm², representing a two-order-of-magnitude decrease compared to the matrix. Combined with scanning electron microscopy, the surface morphologies of various coatings after corrosion were observed, and the corrosion mechanisms of magnesium alloys with these coatings were carefully discussed. Based on electrochemical analysis, this study proposes and verifies that the working mechanism of the composite coatings relies on a physical barrier rather than a redox reaction. Full article

Olive pomace biochar, obtained through the pyrolysis of lignocellulosic biomass, has emerged as a sustainable and multifunctional additive for polymer composites. Its physicochemical properties, including porosity, surface area, and electrical conductivity, can be tailored by controlling feedstock type and pyrolysis conditions. Although mechanical reinforcement and thermal stability improvements are well documented, the influence of biochar on surface-related properties such as wettability and contact angle remains insufficiently explored for environmentally relevant composite systems. In this study, epoxy-based composites containing biochar synthesized at 750 °C were evaluated in terms of their water interaction behavior by monitoring the evaporation dynamics of ultra-pure water droplets (10 μL, 0.055 mS/cm conductivity) at eight time intervals between 20 and 580 s using high-resolution digital microscopy. Image enhancement and segmentation were performed prior to Discrete Cosine Transform (DCT) analysis to describe droplet geometry in the frequency domain. Time-dependent variations in the standard deviations of DCT coefficients were optimized using the Bat Algorithm, resulting in mathematical models capable of accurately representing droplet evolution and surface–fluid interactions. The primary novelty of this study lies in the development of a hybrid experimental–computational framework that integrates droplet-based wettability measurements with signal-domain analysis and metaheuristic optimization. Unlike conventional studies focusing solely on material characterization, this approach establishes quantitative relationships between surface behavior and numerical descriptors derived from DCT and the Bat Algorithm. The proposed methodology provides a data-driven tool for predicting wettability trends in biochar-reinforced composites and supports the development of moisture-resistant materials for coatings, packaging, and thermal insulation applications within the context of sustainable composite design. Full article

To address the capacity decay of NCM811 caused by microcracks and cation disorder during cycling, La, Al, and F tri-doped micron-sized single-crystal NCM811 material with a LiNbO₃ coating was synthesized via a facile co-solvent method. Using a mixed glucose–urea thermal solution as the reaction medium, metal salts were incorporated, followed by step-wise sintering, ball-milling, heat treatment, and wet-chemical coating. This approach enables atomic-level precursor mixing and ensures homogeneous element distribution. La³⁺ enlarges the lithium layer spacing to enhance ion diffusion and Al³⁺ suppresses Ni³⁺ reduction to Ni²⁺, mitigating cation mixing and improving conductivity, while F⁻ stabilizes the crystal structure via its strong electronegativity. The LiNbO₃ coating protects the interface from electrolyte attack, and the single-crystal morphology effectively suppresses microcracking. Compared to unmodified single-crystal NCM811 prepared identically, the modified material exhibits reduced cation disorder, improved crystallinity, and superior thermal stability. Electrochemical tests in half-cells with 1 M LiPF₆/(EC/EMC/DMC) electrolyte (2.8–4.3 V) show an initial discharge capacity of 208.32 mAh/g at 0.1 C and 194.05 mAh/g at 1 C. After 200 cycles at 1 C, the capacity retention remains at 92.21%, exceeding the market average. Rate performance is also notably enhanced, with the 5 C discharge capacity increasing from 141.12 mAh/g (unmodified) to 166.81 mAh/g, demonstrating improved kinetics and structural stability. Full article

In Hungary, a fast-growing Empress tree hybrid (×Paulownia Clone in vitro 112) also known as Smaragdfa^® has been developed as a low-density plantation species seeking industrial utilization. Many potential industrial applications presuppose its bonding. The presence of adhesives in bonded layered assemblies, with differing climatic conditions on the internal and outer side, may induce undesired internal strains due to restricted water vapor diffusion, especially in the case of Smaragdfa as a low-density wood species. For decades, lasures have been specifically formulated with a molecular structure that allows partial vapor transmission while hindering water diffusion. Lasure-coated samples were used as control samples to identify, among the different custom-made MW adhesives, the one with diffusion properties closest to those of the lasure. Uncoated Smaragdfa wood samples were used as the baseline reference to evaluate the effect of different adhesive and coating systems on water vapor diffusion. Smaragdfa samples were prepared both uncoated and coated with different adhesive and lasure layers. Experiments were conducted following ISO 12572 and ASTM E96 standards using the cup method, with all specimens pre-conditioned to 12% moisture content. Results showed that the uncoated Smaragdfa exhibited the highest diffusion coefficient (δ = 7.02 × 10⁻¹³ kg/(m·s·Pa)) and flow rate (G = 0.055763 g/h), while the commercial adhesive-coated sample displayed an 84% reduction in diffusion capacity (δ = 1.15 × 10⁻¹³ kg/(m·s·Pa)), indicating a strong vapor-blocking effect. The lasure coating allowed partial vapor transmission, confirming its semi-permeable nature. Adhesives formulated with varying polyol molecular weights (Series 1–5) revealed a clear molecular-weight-dependent diffusion behavior: low-MW systems (S1) acted as strong diffusion barriers comparable to lasure-coated samples (SMW_L), in the same time high-MW systems (S4, S5) permitted excessive diffusion but induced microcracking, while intermediate formulations (S2, S3) achieved the most balanced performance, combining moderate diffusion with structural stability. Overall, the findings confirm that adhesive layers significantly influence water vapor transmission through Smaragdfa wood, with the degree of hindrance closely related to the molecular weight of the polyol matrix. The optimized formulations (S2, S3) demonstrate promising potential for use in bonded assemblies and engineered wood products where controlled vapor diffusion and mechanical reliability are critical in order to support reduced strains caused by water vapor. Full article

For the first time, hybrid nanocomposites based on poly(2,5-dichloro-3,6-bis(phenylamino)-p-benzoquinone) (PCPAB) and multi-walled carbon nanotubes (MWCNTs) were obtained and the influence of the preparation method on their structure and functional properties was demonstrated. The nanocomposites were obtained both by ultrasonic mixing of PCPAB and MWCNTs, and via in situ oxidative polymerization of CPAB in the presence of MWCNTs or MWCNTs with the addition of ZnO. The formation of hybrid nanocomposites occurs due to non-covalent interaction (π-stacking) between the graphene structures of the MWCNT surface and the phenyl rings of PCPAB. It was found that during the in situ oxidative polymerization of CPAB in the presence of MWCNTs, the growth of polymer chains occurred in close proximity to the filler surface, which led to the formation of a polymer coating. ZnO particles, localized on MWCNTs, on the one hand, prevent their aggregation, and on the other hand, create additional polymerization reaction centers due to the coordination of the Zn-O bond at the H and O atoms of the monomer. An increase in the concentration of reaction centers as a result led to a 2–2.5-fold reduction in the induction polymerization period. According to SEM data, in this case, a more ordered and denser polymer layer is formed due to intermolecular complexation between the main and side chains of the growing polymer with the participation of Zn²⁺ ions formed as a result of the transformation of ZnO to ZnCl₂ in the acidic reaction medium of polymerization. The results of the study of the frequency dependences of conductivity indicate a hopping mechanism of conductivity of nanocomposites. The electrical conductivity of nanocomposites depends on their production method and the MWCNT content and varies between 0.5 and 1.1 S∙cm⁻¹, which is 6–12 times higher than the conductivity of the original polymer. Thermogravimetric analysis revealed that the nanocomposites exhibit enhanced thermal stability compared to PCPAB. The best results were shown by nanocomposites with a higher content of MWCNTs, for which the residual mass at 450 °C was 51–53%. Full article

Single memristive nanowire networks have emerged as a promising pathway for energy-efficient neuromorphic computing, owing to their intrinsic nonlinearity, high dimensionality, fading memory and volatile switching dynamics relevant to physical reservoir computing. While prior works focused on oxide- or silver-based network systems, these approaches face trade-offs between operating voltage, cost, stability, and scalability. This work presents a proof-of-concept demonstration of stochastic polyvinylpyrrolidone (PVP)-coated nickel nanowire networks as low-cost and scalable memristive platforms, exhibiting low-voltage resistive switching (1–2 V). The electrical characterization reveals predominantly volatile resistive switching combined with nonvolatile behavior, consistent with a filamentary conduction mechanism at nanowire junctions. The switching dynamics are governed by the polymer coating thickness, with an intermediate PVP concentration (Ni@PVP = 1:25) showing optimal performance, with a resistance ratio of ~200, stable retention over 1 h, and a reproducible endurance of over 45 cycles. These results establish Ni@PVP nanowire networks as promising memristive platforms for neuromorphic hardware applications and physical reservoir computing, with relevant properties such as fading memory and nonlinear dynamics. Full article

This study aims to develop high-performance hybrid nanocomposites for solid-state energy conversion. We achieved this by improving charge transport and thermoelectric efficiency through the interaction of polymers, nanoparticles, and ionic liquids. Nickel oxide nanoparticles (NiO NPs) were synthesized via a sonochemical route using a novel ionic liquid, 1,2-(propan). In our recent work, this approach enabled the formation of a hybrid [NiO NPs + IL] system, which was subsequently incorporated at different loadings (8, 15, and 30 wt.%) and coated with polyethylene glycol (PEG). The resulting nanocomposites were investigated to elucidate charge-transport mechanisms and assess the influence of the polymer coating on their optical, electrical, and thermal transport properties. Optical measurements showed a shift in the band gap due to π–π* electronic transitions. This effect indicates strong interface interactions. The PEG-coated [NiO NPs + IL] nanocomposites exhibited significantly enhanced charge-carrier mobility, resulting in improved electrical conductivity. Remarkably, a high Seebeck coefficient of 720 μV/K and an electrical conductivity of 0.35 S/cm were achieved, resulting in a maximum power factor of 24.74 μW/m·K², surpassing many recently reported polymer-based nanocomposites. PEG-coated [NiO NPs + IL] systems offer tunable optical properties and superior thermoelectric performance. Consequently, they are a promising alternative to conventional nanocomposites for sustainable energy conversion. Full article

This study investigates the hydrophobic properties of hexamethyldisiloxane (HMDSO)-based coatings deposited by atmospheric pressure plasma-enhanced chemical vapor deposition (AP-PECVD). The objective of this procedure is to enable the extraction of molded components from the mold cavity. The test specimen geometry employed in the present investigation were made of tool steel 1.2311, a material that is frequently utilized in industrial applications. A series of experiments was conducted to assess the coating performance. Initially, surface energy measurements based on contact angle analysis were performed to determine the polar and dispersive surface components. Finally, energy-dispersive X-ray spectroscopy (EDX) and scanning electron microscope (SEM) images are used to perform an exact measurement of the elemental composition and an optical comparison of the surface. The results of the work indicate that the material composition on the surface of silicon and oxygen is of particular importance. In addition, the results indicate that the use of argon as a carrier gas has a positive effect on reducing surface energy and increasing the contact angle to water drops. Full article