Search Results (8,073)

The current study evaluates the characteristics of electrospun PVDF-based membranes doped with zeolite-A in terms of their structural, morphological, thermal, mechanical, hydrophobic, optoelectrical, and adsorption properties. The effects of the DMF–acetone ratio on solvent and zeolite-doping concentration have been evaluated using SEM-EDX, BET, Raman, XRD, DSC-TGA, UV-VIS spectroscopy, contact angle measurements, and mechanical testing. The membranes prepared with solvents low in acetone and increased zeolite content exhibited a higher crystallinity degree exceeding 50%. Zeolite-enriched membranes have a slightly higher content in the α crystalline phase of PVDF when compared to zeolite-free membranes. Electrospinning processing decreased the sample’s subcooling, improving its thermal stability. Zeolite-doping reduced the band gap energy to 1.3 eV from a maximum of 2.7 eV in PVDF membranes. Membranes doped with 3 or 4 wt.% zeolite exhibit improved load-elongation values at break, reaching up to 4.2 N and 47 mm, respectively, and increased flexibility due to their porous structures and the ratio of crystalline to amorphous phases. The membranes adsorbed an MB equilibrium quantity up to 18.5 mg/g and obeyed the pseudo-second-order (PSO) kinetic model within the first 24 h. Thus, the synergistic effect of zeolite content and solvent ratio can effectively adjust the sample’s structure, texture, and properties. Full article

Mg-doped gallium oxide films were prepared on single crystal sapphire substrates through radio frequency magnetron sputtering technology, and then AlN films of different thicknesses were deposited on them as passivation layers. Finally, Pt interdigitated electrodes were prepared through mask plate and ion sputtering technology to make metal–insulator–semiconductor–insulator–metal (MISIM) photodetectors. The influence of the AlN passivation layer on the optical properties and photodetection performance of the device was investigated using UV-Vis (ultraviolet-visible absorption spectroscopy) spectrophotometer and a Keith 4200 semiconductor tester. The device’s performance was significantly enhanced. Among them, the MISIM-structured device achieves a responsivity of 2.17 A/W, an external quantum efficiency (EQE) of 1100%, a specific detectivity (D*) of 1.09 × 10¹² Jones, and a photo-to-dark current ratio (PDCR) of 2200. The results show that different thicknesses of AlN passivation layers have an effect on the detection performance of Mg-doped β-Ga₂O₃ films in the UV detection of the solar-blind UV region. The AlN’s thickness has little effect on the bandgap when it is 3 nm and 5 nm, and the bandgap increases at 10 nm. The transmittance of the film increases with the increase in AlN thickness and decreases when the AlN’s thickness increases to 10 nm. The photocurrent exhibits a non-monotonic dependence on AlN thickness at 10 V, and the dark current gradually decreases. The thickness of the AlN passivation layer also has a significant impact on the response characteristics of the detector, and the response characteristics of the device are best when the thickness of the AlN passivation layer is 5 nm. The responsiveness, detection rate, and external quantum efficiency of the device first increase and then decrease with the thickness of the AlN layer, and comprehensive performance is best when the thickness of the AlN passivation layer is 5 nm. The reason is that the AlN layer plays a passivating role on the surface of Ga₂O₃ films, reducing surface defects and inhibiting its capture of photogenerated carriers, while the appropriate thickness of the AlN layer increases the barrier height at the semiconductor interface, forming a built-in electric field and improving the response speed. Finally, the AlN layer inhibits the adsorption and desorption processes between the photogenerated electron–hole pair and O₂, thereby retaining more photogenerated non-equilibrium carriers, which also helps enhance photoelectric detection performance. Full article

Reactions of anhydrous Zn(II) iodides with redox-active 1,4-diaza-1,3-butadiene (DAD) and its bis(imino)acenaphtene (BIAN) derivatives in absolute acetonitrile yielded a series of new complexes: [(Mes-DAD)ZnI₂] (1), [(dpp-DAD)ZnI₂] (2), and [(dpp-BIAN)ZnI₂] (3). Single crystals of all compounds were obtained, and their molecular structures were unambiguously determined by X-ray diffraction analysis. Purity of bulk samples in solid state was confirmed by PXRD. Stability of the complexes in solution was investigated by means of UV-Vis and NMR spectroscopy. Cyclic voltammetry revealed two or three quasi-reversible reduction waves in the cathodic region for complexes 1–3. The ability of 3 to accept up to three electrons highlights the potential of these compounds as electrocatalysts for reductive transformations. Full article

Plastic-based materials dominate the packaging industry. However, their non-biodegradability has increased the need for sustainable alternatives. Biopolymers, mainly lignocellulose from agricultural residues, offer renewable, eco-friendly options in this context. This study reports the development of lignocellulosic films from alfalfa (Medicago sativa) through green valorization of its biomass. Alfalfa lignocellulosic extract (ALE) was extracted using 50% NaOH, solubilized in 68% ZnCl₂, crosslinked with CaCl₂, and plasticized with sorbitol. The concentrations of ALE, CaCl₂, and sorbitol were optimized using the Box–Behnken Design, focusing on increasing tensile strength (TS), elongation at break (EB), and reducing water vapor permeability (WVP) of the films. The optimized film formulation (0.5 g ALE, 453.8 mM CaCl₂, 1.5% sorbitol) showed a TS of 11.2 ± 0.7 MPa, EB of 5.8 ± 0.9%, and WVP of 1.2 ± 0.2 × 10⁻¹⁰ g m⁻¹ s⁻¹ Pa⁻¹. The film effectively blocked UV–Vis–IR light and exhibited notable antioxidant activity, making it suitable for packaging light-sensitive and oxidation-sensitive foods. Additionally, it achieved over 90% biodegradation within 29 days under 24% soil moisture. These findings demonstrate a sustainable approach to upcycling agricultural residues into functional products, offering a practical alternative to traditional plastics and supporting a circular bioeconomy, while adding value for alfalfa producers. Full article

Green nanotechnology offers a sustainable and eco-friendly approach for nanoframework synthesis. The present study intended to synthesize a novel eco-friendly encapsulated Zeolitic Imidazolate Framework-8 (ZIF-8) in a one-pot method using metabolites from the mangrove plant Conocarpus erectus (CE). Gas Chromatography–Mass Spectrometry (GC-MS) analysis of the extract revealed the presence of important bioactive metabolites. The synthesized material was evaluated by UV-Vis spectroscopy, X-ray diffraction (XRD), particle size analysis (PSA), zeta potential measurement, high-resolution transmission electron microscopy (HR-TEM), and Fourier transform infrared (FT-IR) spectroscopy studies. The environment-friendly mangrove metabolites aided by Zeolitic Imidazolate Framework-8 was found to be crystalline, rhombic dodecahedron structured, and size dispersed without agglomeration. The nanomaterial possessed a broad antimicrobial effect on drug-resistant microorganisms, including Candida krusei, Escherichia coli, Streptococcus Sp., Staphylococcus aureus, Enterococcus Sp., Pseudomonas aeruginosa, Klebsiella pneumoniae, C. propicalis, and C. albicans. Further, its cytotoxicity against MDA-MB-231 cells was found to be efficient. The morphological alterations exhibited by the antiproliferative impact on the breast cancer cell line were detected using DAPI and AO/EB staining. Therefore, ZIF-8 encapsulated mangrove metabolites could serve as an effective biomaterial with biomedical properties in the future. Full article

We report the synthesis, spectroscopic, structural, and ultrafast photophysical investigation of a series of homoleptic and heteroleptic Zn(II) complexes based on the donor-acceptor β-diketonate ligand 4,4,4-trifluoro-1-phenylbutane-1,3-dione. Mass spectrometry, infrared, and NMR analyses confirm complexation and indicate possible fragmentation pathways involving the sequential loss of β-diketonate ligands. Single-crystal X-ray diffraction revealed that all complexes adopt monomeric octahedral geometries, with the ancillary nitrogen-based ligands introducing variable distortions. Thermal analyses confirmed that the complexes are non-volatile and have an onset >250 °C, with thermal decomposition primarily to ZnO and ZnF₂. Complexes with aromatic Lewis base led to higher residue percentages, likely due to the final graphitic carbon content. UV-Vis absorption and femtosecond transient absorption spectroscopy demonstrate that the chelated β-diketonate ring serves as the main optically active chromophore, a property unaffected by the nitrogen ligands. The free ligand undergoes rapid internal conversion, whereas coordination to Zn stabilizes the triplet state via LMCT, producing long-lived and chemically reactive species relevant to dissociation processes. This study demonstrates how tailored ligand environments can be exploited to tune excited-state properties, offering a rational framework for the design of functional precursors suitable for nonlinear photolysis and advanced nanomaterial synthesis. Full article

Carbon quantum dots (CQDs) are photoluminescent nanomaterials (<10 nm) with excellent hydrophilicity, biocompatibility, and low cytotoxicity, making them attractive for biological applications. However, their use in aquaculture nutrition has remained largely unexplored. This study investigated the effects of dietary CQDs on zebrafish (Danio rerio), a model organism with approximately 70% genetic homology with humans. CQDs were synthesized hydrothermally from unripe Citrus limon and characterized by UV–visible (UV-Vis) spectroscopy, UV–vis transillumination, scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray analysis (EDX), Fourier-transform infrared spectroscopy (FT-IR), and photoluminescence (PL) spectroscopy. Zebrafish were fed diets containing varying CQD concentrations, and growth performance, condition factor (K), hematological parameters, enzymatic activity, and tissue morphology were assessed. Feeds supplemented with 2 mL CQDs produced significant improvements in growth and biochemical indicators without adverse effects. Hematological and enzymatic profiles remained within normal ranges, and histological examination revealed no morphological abnormalities, indicating the absence of toxicity. These findings suggest that citrus-derived CQDs can enhance zebrafish growth and maintain physiological health, thereby supporting their potential as safe functional feed additives in aquaculture. This approach may open new opportunities for the application of CQDs in sustainable fish farming and the broader food industry. Full article

Eleven novel asymmetric pyrimidine derivatives were synthesized. The pyrimidine core was functionalized with a coumarin chromophore and a pro-mesogenic fragment bearing either chiral or linear alkyl chains of variable length and substitution patterns. The thermal properties were investigated using polarized optical microscopy, differential scanning calorimetry, and small-angle X-ray scattering, revealing that only selected derivatives exhibited liquid crystalline phases with ordered columnar or smectic organizations. Linear and nonlinear optical properties were characterized by UV–Vis absorption, fluorescence spectroscopy, two-photon absorption, and second-harmonic generation. Optical responses were found to be highly sensitive to the substitution pattern: derivatives functionalized at the 4 and 3,4,5 positions exhibited enhanced 2PA cross-sections and pronounced SHG signals, whereas variations in alkyl chain length exerted only a minor influence. Notably, compounds forming highly ordered non-centrosymmetric mesophases produced robust SHG-active thin films. Importantly, strong SHG responses were obtained without the need for a chiral center, as the inherent asymmetry of the linear alkyl chain derivatives was sufficient to drive self-organization into non-centrosymmetric materials. These results demonstrate that asymmetric pyrimidine-based architectures combining π-conjugation and controlled supramolecular organization are promising candidates for nonlinear optical applications such as photonic devices, multiphoton imaging, and optical data storage. Full article

Metal-free aminobenzoic acid-derived Schiff bases are attractive antimicrobial leads because their azomethine (–C=N–) functionality enables tunable electronic properties and target engagement. We investigated whether halogenation on the phenolic ring would modulate the redox behavior and enhance antibacterial potency, and hypothesized that heavier halogens would favorably tune physicochemical and electronic descriptors. We synthesized three derivatives (SB-3/Cl, SB-4/Br, and SB-5/I) and confirmed their structures using FTIR, ¹H- and ¹³C-NMR, UV-Vis, and HRMS. For SB-5, single-crystal X-ray diffraction and Hirshfeld analysis verified the intramolecular O–H⋯N hydrogen bond and key packing contacts. Cyclic voltammetry revealed an irreversible oxidation (aminobenzoic ring) and, for the halogenated series, a reversible reduction associated with the imine; peak positions and reversibility trends are consistent with halogen electronic effects and DFT-based MEP/LHS descriptors. Antimicrobial testing showed that SB-5 was selectively potent against Gram-positive aerobes, with low-to-mid micromolar MICs across the panel. Among anaerobes, activity was more substantial: Clostridioides difficile was inhibited at 0.1 µM, and SB-3/SB-5 reduced its sporulation at sub-MICs, while Blautia coccoides was highly susceptible (MIC 0.01 µM). No activity was detected against Gram-negative bacteria at the tested concentrations. In the fungal assay, Botrytis cinerea displayed only a transient fungistatic response without complete growth inhibition. In mammalian cells (HeLa), the compounds displayed clear concentration-dependent behavior. Overall, halogenation, particularly iodination, emerges as a powerful tool to couple redox tuning with selective Gram-positive activity and a favorable cellular tolerance window, nominating SB-5 as a promising scaffold for further antimicrobial optimization. Full article

One of the current and serious environmental problems is the pollution due to microplastics. There is an urgent need for biodegradable and bio-based materials for numerous applications, including food packaging. In this work we examine the bio-based polyester cutin for its potential to be used as food packaging material, in terms of migration, based on the Hansen Solubility Parameters (HSP). Cutin is a cross-linked polymer that is swelled by various solvents. We use the degree of swelling of cutin in carefully selected solvents of various polarities in order to estimate the HSP of cutin. Some solvents can induce alteration of the chemical structure of cutin, as proven by Fourier Transform Infrared (FTIR) measurements. This interferes with the process of estimation of the HSP and is discussed in depth. The distance R_a and the Relative Energy Difference (RED) between the HSP of cutin and various food components are calculated and used to predict the existence of favorable interactions between cutin and the food components, which is translated to a high probability for the existence of migration and permeation. Experimental confirmation of one prediction based on HSP is provided by UV-VIS photometry. Similar calculations were performed for other polyesters (poly(lactic acid) and poly(hydroxy butyrate)). Cutin exhibits compatibility with substances of low polarity, such as fats and lipids and non-polar compounds found in essential oils. Thus, migration into fatty foods is expected as well as sorption and permeation of some (volatile) compounds into cutin. Nevertheless, we conclude that the overall migration risk for cutin is lower than the one of other bio-based polyesters. HSP can be used for initial screening of potential migration risks; however, further research is necessary in order to assess the occurrence, extent, and significance of the actual migration. Full article

In this study, molybdenum disulfide (MoS₂)-based water nanofluids were prepared and stabilized using two surfactants with opposite charges: the cationic cetyltrimethylammonium bromide (CTAB) and the anionic sodium lauryl sulfate (SLS). Different MoS₂:surfactant ratios (1:1, 1:2, and 1:3) were examined to identify the optimal formulation ensuring stable dispersion. Stability was evaluated through dynamic light scattering (DLS), zeta potential, and UV–Vis spectroscopy analyses. The results showed that the MoS₂:SLS (1:3) nanofluid achieved the highest stability, characterized by a zeta potential of −38 mV and a mean particle size of approximately 290 nm. Thermophysical properties were then investigated for nanoparticle concentrations of 0.05, 0.1, and 0.2 wt%. The 0.1 wt% nanofluid exhibited the best performance, showing a thermal conductivity enhancement of about 49% and an increased specific heat capacity compared with pure water. This improvement is attributed to uniform nanoparticle dispersion and enhanced phonon transport. Overall, the results demonstrate that the anionic SLS surfactant at a 1:3 ratio effectively enhances the stability as well as the thermal performance of MoS₂–water nanofluids, making them promising candidates for thermal management and energy systems applications. Full article

Cancer remains a major global health challenge, prompting the search for natural therapeutic agents with selective anticancer activity. This study investigated extracts from 12 medicinal plant species (a total of 21 samples) rich in phenolic compounds, particularly ellagic acid and its derivatives, to evaluate their antioxidant properties and ability to inhibit cancer cell viability. Spectrometric analysis and high-performance liquid chromatography (HPLC) with electrochemical detection (ED) and ultraviolet–visible (UV-VIS) detection were used for compound identification. The anticancer activity of plant extracts was tested using the MTS cell proliferation assay to determine anticancer activity on 4T1, A549, Caki-1, HCT116, and MCF7 cancer cell lines. The HEK-293 healthy cell line was used to determine extracts cytotoxicity. Study results indicate that black walnut (Juglans nigra L.), fireweed (Chamaenerion angustifolium L.), and pedunculate oak (Quercus robur L.) have the highest contents of bioactive compounds. Among tested extracts, fireweed showed the lowest IC₅₀ values, thus the strongest anticancer activity against 4T1 cells (IC₅₀ = 0.28 ± 0.01 RE (rutin equivalents) mg/g), while black walnut was most effective against Caki-1 and HCT116 (IC₅₀ = 1.56 ± 0.01; 2.56 ± 0.02 RE mg/g). IC₅₀ values are reported in rutin equivalents (RE) to maintain consistency with antioxidant normalization parameters used throughout the study. Extended incubation increased anticancer activity across most medicinal plant extracts, with fireweed and Canadian goldenrod demonstrating rapid and sustained potency already at 24 h. After 72 h, the most active fireweed extract inhibited approximately 104–190 million cancer cells per gram of dried plant material, demonstrating substantial antiproliferative activity consistent with the IC₅₀ findings. Importantly, none of the extracts showed cytotoxicity to healthy HEK-293 cells. Overall, the findings highlight several plant species with significant anticancer potential, underscoring their promise as sources of natural bioactive compounds for future cancer prevention and treatment research. Full article

Regulatory alerts regarding unauthorized use of colorants in food are frequently issued, often involving excessive concentration, improper declaration, or prohibited dyes. The illegal use of reactive textile dyes in food-related coloring preparations remains largely unrecognized, but confirmed cases have been reported in 2016 and 2020 and most recently in May 2025. This work presents the qualitative analyses’ results of a blue coloring powder for food use with regard to reactive dyes. The sample was labeled as a natural product, although it exhibited the color stability typical of artificial dyes. Prompting further investigation, combined spectroscopic, chromatographic and mass spectrometric methods were applied for the characterization and comparison with reference samples. In agreement with all analyses performed, strong evidence was found that the blue coloring powder contained several identical constituents with a reference sample of Reactive Blue 21. The overall composition suggests that both are complex mixtures of different phthalocyanines, suspected byproducts of synthesis, and various unknown compounds, rendering the powder unsuitable for human consumption. These findings emphasize the importance of tightened analytical controls regarding the unauthorized addition of textile dyes to food in order to maintain consumer safety. Full article

Titanium alloys are widely used in orthopedic and dental implants, yet their limited bioactivity and bacterial resistance remain critical challenges. This study aimed to enhance the surface performance of a Ti-13Zr-13Nb alloy through the formation of a porous oxide layer and the application of a bioactive, drug-loaded coating. Porous oxide layers composed of Ti, Zr, and Nb oxides with fluoride incorporation were fabricated using a novel anodizing process. The fluoride-assisted electrochemical mechanism controlling oxide growth was elucidated through SEM and EDS analyses. The anodized surface exhibited reduced microhardness, beneficial for minimizing stress-shielding effects. Subsequently, chitosan–tetracycline composite coatings were produced via EPD and compared with dip-coating method. Characterization by ATR-FTIR, optical microscopy, SEM, and UV-VIS spectroscopy confirmed the formation of uniform, adherent, and moderately porous coatings with sustained drug release when produced by EPD, while dip-coated layers were less homogeneous and released the drug faster. Microhardness testing revealed improved mechanical integrity of EPD coatings. The developed chitosan–tetracycline–oxide layer system provides tunable nano/microgram-scale drug release and enhanced surface functionality, offering promising perspectives for acute and medium-term regenerative and antibacterial biomedical applications. Full article

Titanium dioxide (TiO₂) thin films sensitized with curcumin were fabricated to investigate the influence of sensitization on their spectroscopic, optical, and photocatalytic properties. TiO₂ films were prepared using different curcumin concentrations and characterized by FTIR, UV–Vis, and diffuse reflectance spectroscopy (DRS). The adsorption kinetics of curcumin on TiO₂ were analyzed, and the photocatalytic performance was evaluated through methylene blue (MB) photodegradation under visible-light irradiation. FTIR spectra confirmed the successful anchoring of curcumin onto the TiO₂ surface, while optical characterization revealed a significant enhancement in visible-light absorption. The band gap decreased from 3.2 eV (pure TiO₂) to 1.8 eV (curcumin-sensitized TiO₂). Furthermore, the curcumin adsorption onto semiconductor data fitted the pseudo-second-order kinetic model, yielding a maximum adsorption capacity of 12.0 mg·g⁻¹. Density Functional Theory (DFT) calculations indicated that ligand-to-metal charge transfer (LMCT) transitions are responsible for the improved visible-light response. Photocatalytic tests demonstrated that all curcumin-sensitized TiO₂ films were active under visible irradiation, confirming curcumin as an effective natural sensitizer for enhancing TiO₂-based photocatalytic coatings. Full article