Search Results (2,387)

In this study, glass fiber-reinforced polymer (GFRP) rebars were fabricated using epoxy resin matrix filled with 5 wt.% of hemp and bamboo powder fillers, both untreated and dielectric barrier discharge (DBD) plasma treated. The tensile, flexural, transverse shear, and pull-out bond strengths were evaluated to investigate the effects of filler type and surface modification. The results show that the incorporation of untreated fillers decreased tensile strength from 706.4 MPa for hemp to 682.3 MPa for bamboo. The plasma-treated hemp formulation demonstrated a higher recovery (762.1 MPa), approaching the control value (804.2 MPa). Transverse shear strength increased from 117.0 MPa (untreated hemp) to 128.3 MPa (plasma-treated hemp). The bond strength with concrete remained unaffected across all groups. Scanning electron microscopy (SEM) revealed improved filler dispersion, reduced voids, and enhanced resin wetting in the plasma-treated specimens. Fourier-transform infrared spectroscopy (FTIR) confirmed the introduction of polar functional groups such as hydroxyl and carbonyl groups onto the fiber surfaces following plasma exposure. These modifications contributed to improved interfacial adhesion and mechanical integrity. Overall, the DBD plasma treatment effectively enhanced the performance and interfacial characteristics of natural fiber-filled GFRP rebars, supporting their potential as sustainable reinforcements in structural applications. Full article

A natural deep eutectic solvent (NADES)-based electropolymerization strategy was developed to deposit polypyrrole (PPy) and Naproxen-doped PPy films onto a biomedical Ti–20Zr–5Ta–2Ag high-entropy alloy. Using cyclic voltammetry, chronoamperometry, and chronopotentiometry, coatings were grown potentiostatically (1.2–1.6 V) or galvanostatically (0.5–1 mA) to fixed charge values (1.6–2.2 C). Surface morphology and composition were assessed by optical microscopy, SEM and FTIR, while wettability was quantified via static contact-angle measurements in simulated body fluid (SBF). Electrochemical performance in SBF was evaluated through open-circuit potential monitoring, potentiodynamic polarization, and electrochemical impedance spectroscopy. Drug-release kinetics were determined by UV–Vis spectrophotometry and analyzed using mathematical modelling. Compared to uncoated alloy, PPy and PPy–Naproxen coatings increased hydrophilicity (contact angles reduced from ~31° to <10°), and reduced corrosion current densities from 754 µA/cm² to below 5.5 µA/cm², with polarization resistances rising from 0.06 to up to 37.8 kΩ·cm². Naproxen incorporation further enhanced barrier integrity (R_coat up to 1.4 × 10¹¹ Ω·cm²) and enabled sustained drug release (>90% over 8 days), with diffusion exponents indicating Fickian (n ≈ 0.51) and anomalous (n ≈ 0.67) transport for potentiostatic and galvanostatic coatings, respectively. These multifunctional PPy–Naproxen films combine robust corrosion protection with controlled therapeutic delivery, supporting their potential biomimetic role as smart coatings for next-generation implantable devices. Full article

This research investigates the impact of incorporating montmorillonite-based nanoclay additives on the anti-corrosive properties of a polyester/triglycidyl isocyanurate (polyester/TGIC) powder coating on phosphated steel. The self-repairing capability facilitated by the swelling and expansion of nanoclay was demonstrated to enhance the corrosion resistance of the coatings significantly. A statistical Mixture Design methodology was employed to establish the optimal combination of nanoclay dosage and coating film thickness. Nineteen experiments were conducted using Design of Experiments, and two regression models were developed using the measured polarization resistance (R_p) and specular gloss values as responses. The mathematical maximization of the R_p value predicted an optimal nanoclay dosage of 4.1% with a corresponding film thickness of 80 µm. Statistical and experimental verification validated the results obtained from the regression models. Notably, the optimized coating demonstrated an R_p value one order of magnitude higher than the coating with 4% nanoclay and a standard film thickness of 60 µm. The behavior of the newly developed coatings was analyzed and compared through measurements of open circuit potential, polarization resistance, and electrochemical impedance spectroscopy. The findings confirm the substantial improvement in the anti-corrosive and self-repairing properties of the polyester/TGIC powder coating with the incorporation of montmorillonite-based nanoclay additives. Full article

Biocompatible coatings are widely employed in dental applications to enhance the biofunctionality of metallic implants exposed to the aggressive oral environment. Among them, hydroxyapatite (HAp)-based and carbide-reinforced coatings have been explored due to their favorable mechanical and biological performance. In this study, Cr₃C_-20(Ni20Cr)-20HAp-XSi coatings were deposited using the high-velocity oxy-fuel (HVOF) technique. The coatings were applied onto commercially pure titanium substrates, with the silicon content varied between X = 0, 5, 10, and 20 wt%. To evaluate the coatings’ corrosion resistance, electrochemical techniques such as potentiodynamic polarization curves, linear polarization resistance (LPR), electrochemical impedance spectroscopy (EIS), and open circuit potential (OCP) were employed. Artificial saliva was used as the corrosive medium at 37 °C for 168 h. The feasibility of producing carbide-HAp-Si coatings with excellent corrosion resistance and cytocompatibility via HVOF was demonstrated here, although some of the tested coatings (20 wt% Si) showed reduced electrochemical stability, attributed to faster dissolution processes and associated with a thinner coating layer, as confirmed by SEM analyses. X-ray diffraction (XRD) analyses revealed the formation of new phases in the coatings during thermal spraying, including Cr₂O₃ and Cr₇C₃. Additionally, MTT assays using 3T3-L1 fibroblasts showed no significant cytotoxic effects after 24 and 72 h of exposure to some of the coatings, confirming their biocompatibility for potential dental applications. Full article

This study investigates the synergistic effects of single- and binary-additive systems on the morphology and nucleation mechanism of Sn-Pb alloy electrodeposited coatings. Scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS), and chronoamperometry were applied in order to obtain more information on the action mechanisms of single-additive systems (cinnamaldehyde, PEG-2000, gelatin, vanillin) and binary ones (0.1 g/L cinnamaldehyde + 0.2 g/L PEG-2000) in Sn-Pb electroplating. Results showed that the use of binary-additive systems based on cinnamaldehyde and PEG-2000 significantly improved coating quality, leading to a smooth and uniform surface, dense grains, and a near-eutectic composition (Sn 63.10 wt.%, Pb 36.90 wt.%). This was because the composite additive, through synergistic effects, exhibited the highest cathodic polarization and the largest charge transfer resistance (189.20 Ω cm²), thus inhibiting the electrodeposition process of Sn²⁺ and Pb²⁺. Chronoamperometry revealed that, unlike single additives (PEG-2000 or cinnamaldehyde), the binary-additive system promoted a transition of nucleation mode to instantaneous nucleation, accompanied by a decrease in the peak current and an extension of the corresponding time. This study provides a theoretical basis and experimental support for understanding the nucleation mode of Sn-Pb electroplating, as well as optimizing the synergistic mechanism of additives. Full article

To address the inherent challenge of poor interfacial compatibility in lignin/poly(butylene adipate-co-terephthalate) (PBAT) composites, lignin was extracted from Camellia oleifera shells and subjected to sequential solvent fractionation using ethanol, acetone, and tetrahydrofuran (THF). Two representative fractions—acetone-soluble (ACL) and THF-soluble (THFL)—were selected for composite preparation with PBAT via solvent casting. The influence of lignin fractionation on the structural and performance characteristics of the resulting composites was systematically evaluated through Fourier-transform infrared (FTIR) spectroscopy, the water contact angle (WCA), differential scanning calorimetry (DSC), tensile testing, and scanning electron microscopy (SEM). The results revealed that the abundant hydroxyl groups and benzene rings present in both ACL and THFL facilitated hydrogen bonding and conjugation interactions with the PBAT matrix, significantly improving interfacial adhesion. Notably, the ACL fraction effectively suppressed phase separation and increased the glass transition temperature (T_g) by 1.9 °C, leading to a 13.9% enhancement in tensile strength compared to neat PBAT. More strikingly, the incorporation of only 7 wt% THFL resulted in a remarkable 31% improvement in tensile strength. This substantial enhancement was primarily attributed to the favorable polarity match between THFL and PBAT, as well as the nucleating effect of THFL, which increased the crystallinity of PBAT by 25.3%. This study highlights the effectiveness of sequential lignin fractionation in tailoring the interfacial properties of biodegradable polymer composites. It also provides a promising strategy for the high-value utilization of lignin toward the development of high-performance, environmentally friendly materials. Full article

This study systematically explored the interaction mechanisms between two KRAS G12C inhibitors (Sotorasib and Adagrasib) and human serum albumin (HSA) via UV-vis spectroscopy, fluorescence spectroscopy, three-dimensional fluorescence spectroscopy, and molecular docking methods. The experimental findings demonstrated that both drugs caused static quenching of HSA fluorescence, with binding constants of 13.64 × 10³ M⁻¹ (Sotorasib) and 63.67 × 10³ M⁻¹ (Adagrasib), demonstrating significant selectivity differences in their binding affinities. UV spectral analysis demonstrated distinct microenvironmental perturbations: Sotorasib and Adagrasib induced a shift (∆λ = 7 nm and ∆λ = 8 nm, respectively) at 211 nm, consistent with altered polarity in HSA’s binding pockets. Fluorescence spectroscopy confirmed a 1:1 binding stoichiometry, with Stern-Volmer analysis validating static quenching as the dominant mechanism. Three-dimensional fluorescence spectra further highlighted Adagrasib’s stronger conformational impact, reducing tyrosine and tryptophan residue fluorescence intensities by 16% (Peak 1) and 10% (Peak 2), respectively, compared to Sotorasib. Molecular docking revealed divergent binding modes: Sotorasib occupied Sudlow Site I via three hydrogen bonds and hydrophobic interactions (∆G = −24.60 kJ·mol⁻¹), whereas Adagrasib bound through one hydrogen bond and hydrophobic forces (∆G = −30.92 kJ·mol⁻¹), with stability differences attributed to structural characteristics. This study uses multispectral technology and molecular docking to reveal the binding mechanism of Sotorasib and Adagrasib with HSA, providing a theoretical basis for designing highly targeted albumin nanocarriers. The strong binding properties of Adagrasib and HSA may reduce the toxicity of free drugs, providing direction for the development of long-acting formulations. Full article

Using ultrasound-assisted extraction, we obtained a chlorophyll-rich extract from Opuntia ficus-indica cladodes (OFI) characterized through thin-layer chromatography (TLC), Fourier-transform infrared spectroscopy (FTIR), and spectrophotometric absorption analysis. The dye exhibited a strong fluorescence response in the visible range (400–800 nm) with a pronounced red emission when excited with a UV source. Antioxidant ability was evaluated via DPPH assay, showing an IC₅₀ of 185 µg/mL, highlighting its potential for reactive oxygen species scavenging. The extract was incorporated into polymethyl methacrylate (PMMA), polyvinylpyrrolidone (PVP), and polyvinyl alcohol (PVA), leading to fluorescence intensity enhancements of up to 40 times compared to the dye alone depending on matrix polarity, consistent with aggregation and polarity effects. Stability tests confirmed the dye’s resistance to CO₂ exposure, pH variations, and prolonged storage, positioning it as a viable alternative to synthetic fluorophores. These findings suggest that the OFI extract provides a functionally relevant, bio-derived dye platform promoting the valorization of agricultural by-products in high-value technological applications, highlighting a circular and scalable approach to developing ecofriendly fluorescent materials, aligning with sustainability and green technology goals. Full article

In this report, we describe the synthesis of a compound derived from the natural compound celastrol, which is connected to a phthalimide moiety via an ester linkage. The compound was fully characterized by proton (¹H), carbon-13 (¹³C), heteronuclear single-quantum coherence (HSQC), and distortionless enhancement by polarization transfer (DEPT) NMR. Ultraviolet–visible spectroscopy (UV-Vis), Fourier-transform infrared (FTIR), and elementary analysis were also performed. Full article

In this research work, the electrochemical evaluation of a non-ionic gemini surfactant as a green corrosion inhibitor for X100 pipeline steel in CO₂-saturated brine solution was carried out by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization curves (PPC). The corrosion inhibition performance of the gemini surfactant was studied in static and hydrodynamic conditions at room temperature and 60 °C. Electrochemical measurements showed that the inhibitor’s performance was enhanced with increasing inhibitor concentration and with increasing exposure time at room temperature, reaching the highest inhibition efficiency (η) at 100 ppm. With increasing temperature, the inhibitor efficiency decreased, with similar behavior at all concentrations. The analysis of the cathodic polarization curves at different rotation speeds showed the strong influence of mass transport on the cathodic process in the absence and the presence of the inhibitor. Under hydrodynamic conditions, PPC and EIS results indicated that the best inhibitor performance was with a concentration of 50 ppm, achieving a maximum inhibition efficiency of 91%. The adsorption of the inhibitor molecules on the surface obeyed the Langmuir isotherm, and the type of adsorption was mixed in all the study conditions. Surface characterization by scanning electron microscopy (SEM) revealed the formation of a protective corrosion inhibitor film. Full article

In this study, cerium with different ratios (x = 0 (zero), 0.1, 0.15, 0.5) was added to the PrMn structure as an A-site material to evaluate characteristic behavior as a potential cathode material for solid oxide fuel cells. The Pr_xCe_1−xMnO_3−δ electrocatalysts were synthesized using the sol–gel combustion method and were assessed for their electrochemical, phase, and structural properties, as well as desorption and reducibility capabilities. Phase changes, from orthorhombic to cubic structures observed upon cerium additions, were evaluated via the X-Ray diffraction method. X-Ray photoelectron spectroscopy (XPS) showed the valence states of the surface between the Ce⁴⁺/Ce³⁺ and Pr⁴⁺/Pr³⁺ redox pairs, while oxygen temperature programmed desorption (O₂-TPD) analysis was used to evaluate the oxygen adsorption and desorption behavior of the electrocatalysts. Redox characterization, evaluated via hydrogen atmosphere temperature-programmed reduction (H₂-TPR), revealed that a higher cerium ratio in the structure lowered the reduction temperature, suggesting a better dynamic oxygen exchange capability at a lower temperature for the Pr_0.5Ce_0.5MnO_3−δ catalyst compared to the electrochemical behavior analysis by the electrochemical impedance spectroscopy method. Moreover, the symmetrical cell tests with Pr_0.5Ce_0.5MnO_3−δ electrodes showed that, when combined with scandia-stabilized zirconia (ScSZ) electrolyte, the overall polarization resistance was reduced by approximately 28% at 800 °C compared to cells with yttria-stabilized zirconia (YSZ) electrolyte. Full article

Conductive composites are a flexible class of engineered materials that combine conductive fillers with an insulating matrix—usually made of ceramic, polymeric, or a hybrid material—to customize a system’s electrical performance. By providing tunable electrical properties in addition to benefits like low density, mechanical flexibility, and processability, these materials are intended to fill the gap between conventional insulators and conductors. The increasing need for advanced technologies, such as energy storage devices, sensors, flexible electronics, and biomedical interfaces, has significantly accelerated their development. The electrical characteristics of composite materials, including metallic, ceramic, polymeric, and nanostructured systems, are thoroughly examined in this review. The impact of various reinforcement phases—such as ceramic fillers, carbon-based nanomaterials, and metallic nanoparticles—on the electrical conductivity and dielectric behavior of composites is highlighted. In addition to conduction models like correlated barrier hopping and Debye relaxation, the study investigates mechanisms like percolation thresholds, interfacial polarization, and electron/hole mobility. Because of the creation of conductive pathways and improved charge transport, developments in nanocomposite engineering, especially with regard to graphene derivatives and silver nanoparticles, have shown notable improvements in electrical performance. This work covers the theoretical underpinnings and physical principles of conductivity and permittivity in composites, as well as experimental approaches, characterization methods (such as SEM, AFM, and impedance spectroscopy), and real-world applications in fields like biomedical devices, sensors, energy storage, and electronics. This review provides important insights for researchers who want to create and modify multifunctional composite materials with improved electrical properties by bridging basic theory with technological applications. Full article

In recent years, the generation of circularly polarized attosecond pulses has garnered significant attention due to their potential applications in ultrafast spectroscopy and, notably, in chiral-sensitive molecular detection. The traditional methods for generating such pulses often involve complex laser configurations or specially engineered targets, limiting their experimental feasibility. In this study, we present a streamlined and effective approach to producing circularly polarized attosecond pulses by employing a linearly polarized laser field in conjunction with a stereosymmetric linear molecule, 1-butyne (C₄H₆). The generation of high-order harmonics by this molecular system reveals a distinct plateau in the perpendicular polarization component, which facilitates the generation of isolated attosecond pulses with circular polarization. Through a detailed analysis of the time-dependent charge density dynamics across atomic sites, we identify the atoms primarily responsible for the emission of circularly polarized harmonics in the plane orthogonal to the driving field. Moreover, we explore the role of multi-orbital contributions in shaping the polarization properties of the harmonic spectra. Our findings underscore the importance of molecular symmetry and the electronic structure in tailoring the harmonic polarization, and they demonstrate a viable pathway for using circularly polarized attosecond pulses to probe molecular chirality. This method offers a balance between simplicity and performance, opening new avenues for practical applications in chiral recognition and ultrafast stereochemical analysis. Full article

Mango (Mangifera indica L.) is cultivated in tropical and subtropical regions, with all parts of the tree—including leaves—used traditionally to treat diabetes, infections, pain, and other conditions. Mango leaves contain proteins, minerals, vitamins, and phenolic compounds, including mangiferin, quercetin, and kaempferol, whose content varies by cultivar. This study evaluated the functional and bioactive properties of dried mango leaves from five cultivars (Julie, DLO, Nam Dok Mai, Irwin, and Keïtt) to determine their potential for food and nutraceutical applications. Analyses included water- and oil-related parameters, swelling and solubility indices, foaming and emulsifying properties, and antioxidant activity (DPPH, ABTS, and FRAP in hydroalcoholic and water extracts), complemented by FT-IR/ATR spectroscopy. Significant differences between the five analyzed cultivars were observed. Irwin exhibited the highest antioxidant activity (2.65 ± 0.55 mg TE/g DM in DPPH assay), while Nam Dok Mai demonstrated superior foaming capacity (82.69 ± 7.79 mL). Strong correlations (r > 0.9) between reducing sugars and antioxidant capacity suggest cultivar selection based on sugar content could predict antioxidant potential. FT-IR confirmed the presence of polar phenolic and protein compounds. The results demonstrate that mango leaves offer cultivar-dependent functional and antioxidant attributes relevant to food systems. Their targeted valorization may support sustainable industrial applications and circular bioeconomy strategies, particularly in tropical regions where mango cultivation is widespread. Full article

This study investigates the effect of copper (Cu) and silver (Ag) additions on the electrochemical behavior of the Fe40Al intermetallic alloy in artificial saliva, aiming to evaluate its potential for biomedical applications such as dental implants. Alloys with varying concentrations of Ag (0.5, 1.0, and 3.0 wt%) and Cu (1.0, 3.0, and 5.0 wt%) were synthesized and exposed to a biomimetic electrolyte simulating oral conditions. Electrochemical techniques, including open circuit potential (OCP), linear polarization resistance (LPR), potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS), were employed to assess corrosion performance. Results show that unmodified Fe40Al exhibits good corrosion resistance, attributed to the formation of a stable passive oxide layer. The addition of Cu, particularly at 3.0 wt%, significantly improved corrosion resistance, yielding lower corrosion current densities and higher polarization resistance and charge transfer resistance values, surpassing even 316L stainless steel in some metrics. Conversely, Ag additions led to a degradation of corrosion resistance, especially at 3.0 wt%, due to microstructural changes and the formation of metallic Ag precipitates, AgSCN, and galvanic cells, which promoted localized corrosion. EIS results revealed that Cu- and Ag-modified alloys developed less homogeneous and less protective passive layers over time, as indicated by increased double-layer capacitance (C_dl) and reduced constant phase element exponent (n_dl) values. Overall, the Fe40Al alloy shows intrinsic corrosion resistance in simulated physiological environments, and Cu additions can enhance this performance under controlled conditions. However, Ag additions negatively affect the protective behavior of the passive layer. These findings offer critical insight into the design of Fe-Al-based biomaterials for dental or biomedical applications where corrosion resistance and electrochemical stability are paramount. Full article