Search Results (242)

7xxx series aluminum alloys are critical structural materials in aerospace applications, but their susceptibility to hydrogen embrittlement (HE) poses significant challenges to service safety and durability. The effects of Si, Er, and Zr microalloying, combined with optimized heat treatments on the HE resistance of Al–Zn–Mg–Cu alloys, were systematically investigated using transmission electron microscopy (TEM), scanning electron microscopy (SEM), and mechanical testing. Three alloys—1# (AlZnMgCuZr), 2# (AlZnMgCuErZr), and 3# (AlZnMgCuSiErZr)—were subjected to single-stage or two-stage homogenization, followed by solution treatments at 470 °C/2 h and 540 °C/1 h, and peak aging at 125 °C. The hydrogen charging experiment was conducted by first applying a modified acrylic resin coating to protect the gripping sections of the specimen, followed by a tensile test. Results demonstrate that alloy 3# with Si addition exhibited the lowest RA_loss, followed by the 2# alloy, which effectively improved the alloys’ hydrogen embrittlement behavior. Compared with the solution in 470 °C/2 h, the 540 °C/1 h solution treatment enabled complete dissolution of Mg₂Si phases, promoting homogeneous precipitation and peak hardness comparable to alloy 2#. Two-stage homogenization significantly enhanced the number density and refinement of L₁₂-structured Al₃(Er,Zr) nanoprecipitates. Silicon further accelerated the precipitation kinetics, leading to more Al₃(Er,Zr) nanoprecipitates, finely dispersed T′/η′ phases, and lath-shaped GPB-II zones. The GPB-II zones effectively trapped hydrogen, thereby improving HE resistance. This work provides a viable strategy for enhancing the reliability of high-strength aluminum alloys in hydrogen-containing environments. Full article

Metal nanoparticles (NP) are increasingly used in biomedical applications. Among them, silver NPs (AgNPs) are used as active components in antibacterial coatings for wound dressings, medical devices, implants, cosmetics, textiles, and food packaging. On the other hand, AgNPs can be toxic to humans, depending on the dose and route of exposure, as agents delivering silver to cells. The cysteine residues are the primary molecular targets in such exposures, due to the high affinity of Ag⁺ ions to thiol groups. The Endothelial monocyte-activating polypeptide II (EMAP II), a cleaved C-terminal peptide of the intracellular aminoacyl-tRNA synthetase multifunctional protein AIMP1, contains five cysteines exposed at its surface. This prompted the question of whether they can be targeted by Ag⁺ ions present at the AgNPs surface or released from AgNPs in the course of oxidative metabolism of the cell. We explored the interactions between recombinant EMAP II, tRNA, and AgNPs using UV-Vis and fluorescence spectroscopy, providing insight into the effects of AgNPs dissolution kinetics on interaction EMAP II with tRNA. In addition, the EMAP II fragments binding to intact AgNPs were established by heteronuclear ¹H-¹⁵N HSQC spectra utilizing a paramagnetic probe. Structural analysis of the EMAP II reveal that the 3D structure of protein was destabilized (partially denatured) by the binding of Ag⁺ ions released from AgNPs at the most exposed cysteines. Surprisingly, this effect enhanced tRNA affinity to EMAP II, lowering its $K_d$. The course of the EMAP II/tRNA/AgNP reaction was also modulated by other factors, such as the presence of Mg²⁺ ions and TCEP, a thiol-group protector used to mimic the reducing conditions of the cell. Full article

Two amide-preformed aromatic diamine monomers, N,N-bis(4-(3-aminobenzamido)phenyl)-N’,N’-bis(4-methoxyphenyl)-1,4-phenylenediamine (m-6) and N,N-bis(4-(4-aminobenzamido)phenyl)-N’,N’-bis(4-methoxyphenyl)-1,4-phenylenediamine (p-6), were synthesized and utilized to prepare two series of electroactive poly(amide-imide)s (PAIs) through a two-step polycondensation reaction with commercially available aromatic tetracarboxylic dianhydrides. The obtained polymers exhibited solubility in various polar organic solvents, and most of them could form transparent, flexible films via solution casting. Thermal analysis indicated glass transition temperatures (T_g) ranging from 250 °C to 277 °C, as measured by DSC, with no significant weight loss observed before 400 °C in TGA tests. Cyclic voltammograms (CV) of the polymer films on ITO-coated glass substrates revealed two reversible oxidation redox pairs between 0.67 and 1.04 V vs. Ag/AgCl in an electrolyte-containing acetonitrile solution. The PAI films showed stable redox activity with high optical contrast both in the visible and near-infrared regions, transitioning from colorless in the neutral state to green and blue in the oxidized states. Furthermore, the polymer films retained good electrochemical and electrochromic stability even after more than 100 cyclic switching operations. The PAIs displayed outstanding electrochromic performance, including high optical contrast (up to 95%), rapid response times (below 4.6 s for coloring and 5.7 s for bleaching), high coloration efficiency (up to 240 cm²/C), and low decay in optical contrast (less than 5% after 100 switching cycles for most PAIs). Full article

Nanomaterials are widely used in biomedical research as drug and antibody carriers, and some nanomaterials have been shown to exhibit antimicrobial activity. Previously, silver nanoclusters (AgNCs) were predicted to interact with the bacterial TolC protein, which is involved in the development of multidrug resistance in pathogens. In this study, glutathione-coated AgNCs were synthesized and characterized. Their toxicological properties were studied in a microplate assay against five bacterial strains, both as single components and in mixtures with heavy metal salts and antibiotics. The resulting AgNCs had a diameter of 2.2 ± 0.5 nm, with excitation and emission maxima of λ = 490 nm and λ = 638 nm, respectively. No significant growth inhibition was observed at the concentrations used in resistance modulation assays (≤2.5 µg/mL Ag), except for transient effects at very high concentrations. A decrease in bacterial resistance to copper (II) and cadmium (II) cations and the antibiotics erythromycin and levofloxacin was observed upon the addition of AgNCs containing 2.5 μg/mL silver to the nutrient medium. A dose-dependent effect of AgNCs on bacterial resistance to toxicants was established. Thus, nanoclusters can be considered as inhibitors of bacterial resistance to heavy metals and antibiotics, which may be useful in studying bacterial adaptation mechanisms and developing technologies for overcoming multidrug resistance in bacteria. Full article

Sustaining irrigated agriculture under drought conditions with alternative water sources such as saline groundwater requires understanding their effects on salt-tolerant crops like pistachio. During recent California droughts, pistachio trees planted in 2002, 2009, and 2011 were irrigated with high-saline water containing traces of boron (B) and selenium (Se). In 2018, irrigation was divided so that half of the trees received low-saline water, while the others continued under high-saline irrigation. Three years later, nuts were harvested to evaluate how irrigation quality affected seed coats, the main storage site of phenolic antioxidants. Sixty seed coat extracts from both irrigation treatments were analyzed for antioxidant capacity (ABTS, DPPH, FRAP and Folin–Ciocalteu assays). Nuts from the oldest trees (planted in 2002) had the highest antioxidant capacity. High-performance liquid chromatography (HPLC) identified gallic acid and nine flavonoids. Catechin, procyanidin B1, cyanidin-3-O-galactoside, and eriodictyol were most abundant in the oldest trees. Irrigation salinity significantly affected gallic acid, quercetin, and isoquercetin, with higher concentrations detected in seed coats from trees receiving continued high-saline irrigation. These compound-specific shifts, together with strong age-dependent patterns, provide insight into how long-term salinity exposure influences phenolic composition in pistachio seed coats. Full article

In this study, 8-ply 3K carbon fiber fabrics were spray-coated with Ag/RGO nanoparticles at varying weight ratios (0, 2.5, and 5 w/w). Composite specimens were fabricated, consisting of an unmodified control sample (neat) and three different variants containing 0.075 w/w% RGO, 0.26 w/w% AgRGO, and 0.45 w/w% AgRGO, respectively. The effects of RGO and AgRGO contents on the electrical conductivity, flexural properties, dynamic mechanical properties, and electromagnetic interference shielding (EMI) performance of these composites were investigated. Additionally, the distribution of RGO and AgRGO on the surfaces and interfaces of carbon fibers was examined using field emission scanning electron microscopy to determine the microstructure–property relationship. The increase in the Ag ratio in the AgRGO filler material in the composite from 2.5 to 5 resulted in an increase in both the through-the-thickness and surface conductivity values by 3.5 times, reaching maximum conductivity values (273 × 10⁻³ S/m and 256 × 10⁻³ S/m, respectively). Composites containing filler material with an Ag/RGO weight ratio of 2.5 achieved a total electromagnetic shielding efficiency of 18 dB at the X-band frequency region, without loss in flexural strength, while the maximum total electromagnetic shielding efficiency value of 22.68 dB was obtained when the Ag/RGO weight ratio was 5. With a maximum SE_T value these composites might be suitable for use in areas that do not require primary load-bearing applications, such as satellite, antenna, and avionics system housings. Full article

The growing demand for environmentally friendly materials has driven extensive research into biopolymer-based nanocomposites with enhanced functional performance. Chitosan, a naturally derived polysaccharide, offers excellent film-forming ability, biodegradability, and antimicrobial potential, making it a promising matrix for sustainable packaging and coating applications. In this study, a distinctive solvent-casting strategy was employed to fabricate chitosan-based nanocomposite films functionalized with dual-action silver/titania (Ag/TiO₂) nanoparticles, combining both photocatalytic and metallic antimicrobial mechanisms—an approach that provides broader functionality than conventional single-component fillers. The biodegradable films were systematically characterized for their structural, mechanical, optical, and barrier properties, as well as their antimicrobial performance. The integration of Ag/TiO₂ imparted unique synergistic effects, modifying film morphology and color, slightly reducing tensile strength, and enhancing hydrophobicity and structural compactness. The obtained water vapor permeability values (0.013–0.102 g·mm·m⁻²·h⁻¹·kPa⁻¹) classified the materials as moderate barriers, comparable to or better than many existing chitosan-based systems without nanofiller reinforcement. Notably, films containing 10 wt% Ag/TiO₂ achieved a 40.4% reduction in Escherichia coli viability and an 8.2% inhibition of Staphylococcus aureus, demonstrating concentration-dependent antimicrobial activity superior to that of neat chitosan films. Overall, the unique combination of a biodegradable chitosan matrix with multifunctional Ag/TiO₂ nanofillers offers clear advantages over traditional biopolymer films, highlighting their potential as advanced materials for active food packaging and antimicrobial surface coatings. Full article

This study investigates the optimization of sol–silicate façade coatings modified with colloidal silica and a silane-based hydrophobizing additive to enhance hydrophobicity while maintaining a high water-vapor transmission rate (V). The effects of the binder ratio between potassium water glass (WG) and colloidal silica (CS), the type of colloidal silica (unmodified or epoxy-silanized), and the concentration of the hydrophobizing additive (HA) were systematically evaluated. Water-vapor transmission was determined according to EN ISO 7783, and surface wettability was measured before and after accelerated UV-A aging. Dynamic viscosity was monitored for two years to assess long-term storage stability. The optimized formulation contained 7 wt % potassium water glass, 15 wt % colloidal silica, and 1 wt % hydrophobizing additive. It exhibited stable viscosity over time (≈19,000 mPa·s after six months), high water-vapor transmission (V > 6700 g·m⁻²·d⁻¹, class V1), and an initial contact angle of 118°, which decreased only moderately after UV-A exposure. Coatings containing epoxy-silanized colloidal silica showed slightly lower transmission but still remained within the high V range suitable for vapor-open façade systems. The results confirm that balanced sol–silicate systems can combine durable hydrophobicity with long-term rheological and functional stability. Full article

Bisphenol A, Bisphenol S, and Bisphenol F are widely used plastic additives and endocrine-disrupting chemicals with potential adverse health effects. Limited research has examined lifestyle and dietary factors influencing human exposure to these compounds. This study investigated associations between urinary bisphenol concentrations and demographic, lifestyle, dietary, and food-handling factors in 4239 Korean adults aged 19 to 82 years (1889 men, 44.6%; 2350 women, 55.4%) from the Korean National Environmental Health Survey (2018–2020). Median urinary concentrations with interquartile ranges were 1.15 µg/L (IQR: 0.45–2.27) for BPA, 0.17 µg/L (IQR: 0.06–0.41) for BPF, and 0.15 µg/L (IQR: 0.06–0.38) for BPS. Urinary bisphenol concentrations differed significantly by gender, age, smoking status, alcohol consumption, and education level (p < 0.001), with higher concentrations in younger males, smokers, and alcohol consumers. Frequent consumption of instant noodles, microwaveable foods, canned foods, and plastic-wrapped takeout was significantly associated with elevated bisphenol levels (p < 0.001). Use of plastic containers, coated cookware, and electric rice cookers was linked to higher urinary BPA and BPS concentrations. BPA showed statistically significant but weak positive correlations with serum creatinine (r = 0.044, p < 0.05) and height (r = 0.037, p < 0.05), as assessed using Pearson’s correlation test. BPF was negatively correlated with aspartate aminotransferase (AST) levels (r = −0.042). Public health strategies should prioritize safer food storage practices and enhance awareness of health risks associated with these chemicals. Full article

This work describes the preparation and characterization of chitosan-based biopolymer coatings containing silver, zinc, and hydroxyapatite nanoparticles deposited on the Ti13Zr13Nb alloy by the EPD method. It was intended to evaluate the influence of surface pretreatments and deposition parameters on the structural, electrochemical, and biological properties of coatings. The morphology and composition were characterized by means of SEM/EDS, AFM, XRD, and FTIR analysis. The obtained results indicated uniform continuous layers with homogeneously distributed nanoparticles and the presence of characteristic functional groups originating from chitosan and hydroxyapatite. Corrosion investigations performed in SBF solution revealed a significant enhancement in corrosion resistance for chitosan/nanoAg/nanoZn/nanoHAp coatings, reflected in a drastic decrease in corrosion current density compared with uncoated Ti13Zr13Nb alloy. The contact angle measurements confirmed their hydrophilic nature, which favors better biointegration ability. Biological tests (MTT and LDH) performed on human osteoblasts (hFOB 1.19) confirmed high biocompatibility (>85% cell viability) in the case of all coatings with the addition of hydroxyapatite, whereas in the case of coatings without HAp, cytotoxicity was observed, probably due to the uncontrolled release of metallic nanoparticles. These findings suggest that the presence of hydroxyapatite in chitosan-based coatings efficiently enhances corrosion protection and cytocompatibility, showing very good prospects for biomedical applications such as the surface modification of titanium implants. Full article

The aim of this study was to investigate the nucleation, growth, and surface deposition of poly(2,2,2-trifluoroethyl methacrylate) [poly(TFEMA)] from the one-phase, cloud point, and two-phase regions of a supercritical CO₂–toluene solvent. A ternary mixture of 20 wt% toluene + 79 wt% scCO₂ + 1 wt% poly(TFEMA) at 40.0 °C was exposed to a fluorine-doped tin oxide (FTO) surface for 30 min at pressures placing the solution in (i) a one-phase region (15.86 MPa), (ii) the cloud point (12.37 MPa), and (iii) a two-phase region (8.96 MPa). Using the Altunin–Gadetskii–Haar–Gallagher–Kell (AG–HGK) equation of state (EOS), the corresponding CO₂ densities are 793.9, 729.2, and 477.8 kg m⁻³. Scanning electron microscopy (SEM) and particle-size analysis (sample sizes N = 852–1177) show particle-size distributions (PSDs) that are well described by the following lognormal form: the mean diameter increases monotonically with a decrease in pressure (1.767 μm → 2.605 μm → 2.863 μm), while dispersion tightens slightly near the cloud point (coefficient of variation, CV: ≈0.47 → 0.44) and then broadens strongly in the two-phase region (CV ≈ 1.02). Morphologies transition from sparse, compact islands (one-phase) to agglomerated, necked spheres (cloud point) and finally hierarchical populations containing hollow/pitted large particles (two-phase). These outcomes are consistent with a phase-state-controlled shift in nucleation pathways, as follows: from heterogeneous surface nucleation in the one-phase regime to homogeneous nucleation with agglomeration at the cloud point, and to homogeneous nucleation with coalescence and solvent capture in the two-phase regime. The results provide a mechanistic basis and practical design rules for pressure-programmable control of fluoropolymer coatings prepared from scCO₂/aromatic-cosolvent systems. Full article

This study investigates the influence of Ag addition on the microstructure, mechanical behavior, corrosion resistance, and antibacterial performance of Mg-Zn-Ca-Ag alloys and their micro-arc oxidation (MAO) coatings. Four casting alloys containing 0.2, 0.4, 0,6 and 0.8 wt.% Ag were fabricated and characterized by SEM, XRD, and TEM. The microstructure consisted mainly of α-Mg, Mg₂Ca, Mg₇Zn₃, and Mg₆Ca₂Zn₃ phases, and the elastic modulus (~25.8 GPa) was comparable to that of human bone. MAO coatings produced in a bio-functional electrolyte exhibited pit-like morphologies due to Ag-induced melt fluidity and self-sealing effects. The coatings were composed primarily of MgO, Mg₂SiO₄, Ca₃(PO₄)₂, CaCO₃, and Ag₂O, with the ZQ 0.8-MAO sample showing the highest Ca/P ratio (1.75), indicative of superior bioactivity. Electrochemical impedance spectroscopy revealed optimal corrosion resistance (2.56 × 10⁴ Ω·cm²), while antibacterial efficiency exceeded 96%. Overall, Ag alloying enhanced both the bulk and surface properties of Mg-Zn-Ca alloys, yielding robust, corrosion-resistant, and antibacterial coatings with excellent biocompatibility-highlighting their potential for biodegradable orthopedic implant applications. Full article

Implementation of novel antiviral coatings and textiles, which can be utilised in the production of personal protective equipment, has the potential to enhance public health security against future pandemic outbreaks. Respiratory viruses, particularly SARS-CoV-2, responsible for COVID-19, have emerged as a major global concern due to their rapid transmission and high mortality rates, leading to nearly seven million deaths worldwide between 2020 and 2025. This statistic underscores the necessity for the development and implementation of advanced antiviral materials to prevent viral infections. This research focused on the in vitro evaluation of the antiviral properties of three antibacterial compounds containing silver (Ag) that were functionalized with coatings. We assessed onsite synthesised Ag powder in comparison to commercially available antibacterial additives, which included nanosilver on colloidal silica (AgSiO₂) and silver sodium hydrogen zirconium phosphate (AgNaOPZr), as potential antiviral agents in coatings against human coronavirus (HCoV). Antiviral assessments revealed that coatings containing Ag at higher concentrations (2.5 and 5%) exhibited limited antiviral effectiveness, with a titer reduction in log < 2. In contrast, the functionalization of AgSiO₂ on coatings significantly suppressed viral replication resulting in a notable reduction in virus titer of log ≥ 2 for all tested concentrations. Full article

In recent years, wine producers have increasingly experimented with ancient fermentation and ageing techniques, such as the use of ceramic containers or pitch-coated amphorae. Despite growing interest in these traditional practices, few studies have investigated the chemical composition of the resulting wines. This is the first study that characterises pine pitch, historically used as a coating material, and evaluates the impact of pitched pottery vessels on the winemaking process and wine composition using a foodomics approach. Vinification was carried out in both pitch-coated and uncoated (control) clay containers. Chemical differences between must and wine produced in pitched and unpitched vessels were assessed using targeted and untargeted ultra-performance liquid chromatography–tandem mass spectrometry (UPLC-MS/MS). Compared to the control, must and wine from the pitch-coated vessels had higher concentrations of many polyphenols such as anthocyanins, coumaric acid and tartaric acid, while procyanidins were present in significantly lower amounts. These findings reveal that pitch-coated ceramic vessels significantly influence wine composition, offering a first step toward deeper investigations into how fermentation environments shape metabolite profiles. This knowledge not only enhances our understanding of traditional practices but also opens new avenues for innovation in contemporary oenology. Full article

Objective: The Ti6Al4V titanium alloy is widely used for dental implants because of its excellent mechanical properties, corrosion resistance, and biocompatibility. However, its bioinert surface limits both osseointegration and resistance to bacterial colonization. Methods: To address these challenges, this study develops a composite coating based on calcium phosphate (CaP) and silver (Ag), reinforced with zirconium oxide (ZrO₂). The coating was deposited on Ti6Al4V using an immersion technique to improve the surface properties of the alloy. Electrochemical analyses (OCP, EIS, and potentiodynamic polarization) were performed in simulated physiological conditions to evaluate the corrosion behavior, while SEM/EDS was used to characterize the surface morphology and composition. Results: The Ag- and Zr-containing CaP coatings significantly improved the corrosion resistance of Ti6Al4V compared with uncoated and CaP-coated samples. Conclusions: This approach provides a promising strategy to enhance the electrochemical stability and long-term durability of titanium dental implants, thereby contributing to their reliable performance in the oral environment. Full article