Search Results (1,222)

Metal ions exemplify one of the most harmful and environmentally detrimental contaminants of water systems. This work describes the creation of an innovative chelated carbon-doped nickel and titanium oxide (C-NiTiO₂) hybrid as an adsorbent for the effective elimination of metal ions. The dominance of the TiO₂ anatase phase with a ≈ 61 nm crystallite size was verified by XRD and Raman investigation. Morphology investigations exposed polygonal nanoparticles consisting of Ti, C, Ni, and O. The nanostructure exhibited a surface area of 17 m²·g⁻¹, a pore diameter of ≈1.5 nm, and a pore volume of 0.0315 cm³·g⁻¹. The nanostructure was evaluated for the elimination of Zn (II) ions from an aqueous solution. The metal ion adsorption onto the hybrid nanomaterial was described and comprehended using adsorption kinetics and equilibrium models. The adsorption data matched well with the pseudo-second-order kinetics and Langmuir adsorption models, indicating a monolayer chemisorption mechanism and achieving a maximum Zn (II) ion elimination of 369 mg·g⁻¹. Mechanistic investigation indicated film diffusion-controlled adsorption through inner-sphere complexation. The nanosorbent could be regenerated and reused for four rounds without appreciable activity loss, thus demonstrating its potential for water cleanup applications. Full article

Zinc-based alloys are promising candidates for biodegradable implant applications; however, their rapid initial corrosion and limited cytocompatibility remain major challenges. In this study, a Zn-Ca-P layer in a form of parascholzite (CaZn₂(PO₄)₂·2H₂O) was prepared on a Zn-0.8Mg-0.2Sr alloy via anodic oxidation followed by short-time biomimetic calcium–phosphate deposition. The formation mechanism, corrosion behaviour, and preliminary biological response of the modified surface were systematically investigated. The Zn-Ca-P layer formed a compact and crystalline phosphate layer that significantly altered the corrosion response of the zinc substrate in Leibovitz L-15 medium containing foetal bovine serum. Electrochemical measurements revealed a pronounced improvement in corrosion resistance and a transition from rapid active dissolution to a controlled, ion-exchange-driven degradation mechanism. The moderate solubility of parascholzite enabled the gradual release of Zn²⁺ and Ca²⁺ ions while maintaining surface stability during immersion. Preliminary cell adhesion experiments demonstrated a clear enhancement of cytocompatibility for the Zn-Ca-P-layer-coated samples, where cells readily adhered and spread, in contrast to the bare alloy surface, which showed lower cell attachment. The improved biological response is attributed to the phosphate-rich surface chemistry, favourable surface morphology, and moderated corrosion behaviour. Overall, the parascholzite-like layer provides an effective strategy with which to regulate both corrosion and early cell–material interactions of zinc-based biodegradable alloys, highlighting its potential for temporary biomedical implant applications. Full article

The shift toward sustainable packaging requires biodegradable, active alternatives. This study developed ternary nanohybrids by loading carvacrol (CV) or trans-cinnamaldehyde (tCN) onto zinc oxide/natural zeolite (ZnO/NZ) hybrids, which were incorporated into a poly-L-lactide/tri-ethyl citrate (PLA/TEC) matrix via melt extrusion to produce active films. A key finding was the distinct interaction mechanism: tCN underwent strong chemisorption with ZnO, creating a sustained-release reservoir, while CV was predominantly physisorbed, leading to rapid release. This interfacial divergence dictated functional performance. Antibacterial assessment of nanohybrids revealed that tCN@ZnO/NZ0.25 exhibited the highest inhibition zones against pathogens, correlating with its chemisorbed reservoir. In films, however, CV-based formulations (especially CV@ZnO/NZ0.25) showed superior immediate antioxidant activity (EC₅₀, ~DPPH~ = 34.43 mg/mL) and an 82% reduction in oxygen permeability. In contrast, tCN-based films (especially tCN@ZnO/NZ1.0) demonstrated superior, sustained antibacterial efficacy. In a minced pork preservation study, both films delayed lipid oxidation and preserved heme iron, while the tCN-based film provided better long-term microbial control. This work demonstrates that engineering the nanocarrier–active compound interface enables precise tailoring of release kinetics, which can be optimized for either high immediate antioxidant power or long-term antimicrobial action, depending on specific food preservation requirements. Full article

Developing sustainable and molecularly selective adsorbents for heavy-metal removal remains a critical challenge in water purification. Herein, we report a green molecular-engineering approach for fabricating aza-crown ether functionalized sodium alginate aerogels (ACSA) capable of highly selective Cu²⁺ capture. The aerogels were synthesized via saccharide-ring oxidation, Cu²⁺-templated self-assembly, and reductive amination, enabling the covalent integration of aza-crown ether motifs within a hierarchically porous biopolymer matrix. Structural analyses (FTIR, ¹³C NMR, XPS, SEM, TGA) confirmed the in situ formation of macrocyclic N/O coordination sites. Owing to their interconnected porosity and chemically stable framework, ACSA exhibited rapid sorption kinetics following a pseudo-second-order model (R² = 0.999) and a Langmuir maximum adsorption capacity of 150.82 mg·g⁻¹. The material displayed remarkable Cu²⁺ selectivity over Zn²⁺, Cd²⁺, and Ni²⁺, arising from the precise alignment between Cu²⁺ ionic radius (0.73 Å) and crown-cavity dimensions, synergistic N/O chelation, and Jahn-Teller stabilization. Over four regeneration cycles, ACSA retained more than 80% of its original adsorption capacity, confirming excellent durability and reusability. This saccharide-ring modification strategy eliminates crown-ether leaching and weak anchoring, offering a scalable and environmentally benign route to bio-based adsorbents that combine molecular recognition with structural stability for efficient Cu²⁺ remediation and beyond. Full article

Zinc (Zn) in excess is very toxic for plants and can limit agriculture. Carbon-based engineered nanomaterials with high electron mobility and electron-accepting capability may be essential for mitigating heavy metal stress. In the present study, the protective role of some fullerene C₆₀ derivatives (fullerenol [C₆₀(OH)_22–24] and the arginine C₆₀ [C₆₀(C₆H₁₃N₄O₂)₈H₈]) were tested for the first time against Zn toxicity in Cucumis sativus L. (cucumber). Plants were grown hydroponically at three concentrations of fullerenes (0, 2, and 10 mg L⁻¹) without or with 40 µM Zn for 17 days. Plant growth, leaf chlorosis, and nutritional imbalances in combination with a metabolomics approach were analyzed. The Zn-treated plants show chlorotic leaves, the retarded growth of shoots (−20%), and roots (−49%) and nutrient imbalance. Addition of fullerene C₆₀ derivatives suppressed loss in the dry biomass of leaves (15%) and roots (40%; fullerenol only) induced by high Zn. However, they did not alter leaf chlorophyll, shoot dry biomass, and elemental composition, including leaf Zn. Moreover, the Zn of xylem sup from roots remained unchanged by fullerenes. In an adsorption experiment, the amounts of Zn adsorbed by tested C₆₀ were below the detection limits. The addition of C₆₀ derivatives slightly changed the metabolite profiling in stressed plants. Nevertheless, in fullerene-treated plants, the abundance of some Zn-responsible metabolites tended to be altered in the opposite direction as compared with the metabolic responses to excessive Zn alone. There were several up-regulated metabolites protecting plants under oxidative stress. We speculate that fullerene C₆₀ derivatives have the ability to increase antioxidant non-enzyme activity at least, improving some growth parameters. However, fullerenes did not reduce Zn transport from the root to the shoots. We concluded that the low capacity of these compounds to buffer Zn in the root zone might limit the efficiency of fullerene derivatives against Zn toxicity. Our results provide new evidence for the crucial role of Zn–fullerene interactions in the amelioration of Zn toxicity in plants. Full article

Based on a novel semi-continuous casting mold with independent primary cooling regulation, a large-size Mg-9.4Gd-5.8Y-1Zn-0.5Zr alloy billet (Ø330 mm) was successfully fabricated via differential phase electromagnetic vibration casting. This process significantly improved microstructural homogeneity, with grain sizes ranging from 117 µm to 130 µm across the billet and elemental segregation of Gd and Y below 3%. Homogenization at 520 °C for 5 h effectively dissolved grain boundary eutectic phases; promoted diffusion of Gd, Y, and Zn into the α-Mg matrix; and stimulated the precipitation of fine LPSO lamellae. These microstructural improvements resulted in an excellent tensile strength of 208.4 MPa and elongation of 24.4%, demonstrating an optimal strength–ductility balance achieved through precise thermal processing. Full article

In this study, ZnO–GO nanocomposites were synthesized from waste Zn–C batteries and used for the photocatalytic degradation of malachite green (MG) under UV light. ZnO–GO nanocomposites with different GO contents (1, 2.5, and 5 wt%) were prepared at room temperature and characterized by XRD, SEM, EDS, and UV–Vis spectroscopy. The GO content significantly affects the morphology, optical properties, and photocatalytic activity of the nanocomposites. In the presence of ZnO NPs, a malachite green degradation efficiency of 96.25% was achieved in 90 min, while ZnO–1%GO, ZnO–2.5%GO, and ZnO–5%GO achieved 95.35%, 97.27%, and 99.6% MG degradation, respectively, in just 30 min. The photocatalytic degradation process of MG was optimized using Response Surface Methodology (RSM). The effects of GO content, catalyst dosage, initial MG concentration, and irradiation time on the efficiency of photocatalytic degradation were investigated, and optimal conditions were determined. Under optimal conditions, a photocatalytic degradation efficiency of 98.51% was achieved. These results indicate that ZnO–GO nanocomposites synthesized from waste Zn–C batteries are efficient and environmentally friendly photocatalysts for the treatment of dye-contaminated wastewater. Full article

Water-based drilling fluids (WBDFs) are widely used due to their economic and environmental advantages; however, shale hydration remains a major limitation. This study evaluates Fe₂O₃, CuO, ZnO, and MgO nanocrystalline metal oxides synthesized via co-precipitation as inorganic shale inhibitors for WBDFs. Comprehensive characterization confirmed phase-pure nanocrystalline oxides (17–38 nm) with high thermal stability. Performance tests revealed that MgO-based WBDF exhibited the lowest plastic viscosity (17 cP), the highest pH (≈10.0), and the strongest shale inhibition (6.1% swelling), while Fe₂O₃ provided superior filtration control (6.0 mL). CuO showed balanced rheology, whereas ZnO displayed comparatively weaker inhibition. Compared with commercial inhibitors (Amine NF and Glycol), MgO- and Fe₂O₃-based systems achieved comparable or improved performance with enhanced thermal and environmental robustness. These results demonstrate the potential of nanocrystalline metal oxides as sustainable additives for improving WBDF performance under high-pressure, high-temperature (HPHT) conditions. Full article

This work investigated the effects of gamma irradiation on the adsorption capacities of rice husk (RH) for the removal of Cu²⁺, Cr³⁺, and Zn²⁺ ions from aqueous solutions, with potential applications in wastewater remediation. RH samples were gamma-irradiated at doses up to 40 kGy and characterized using SEM-EDS, XRF, FTIR, XRD, and BET analyses. While morphological and textural changes remained subtle, FTIR and SEM-EDS confirmed the formation and intensification of oxygen-containing functional groups, including –OH, –COOH, and C=O, as well as increased exposure of silica (Si–O) on the surfaces, which substantially enhanced surface reactivity of RH toward metal ions. Batch adsorption experiments revealed that 40-kGy irradiated RH samples (RH-40) exhibited the highest removal efficiencies compared to non-irradiated and lower-dose samples (RH-0, RH-10, RH-20, and RH-30), specifically with improvements of 415% for Cu²⁺, 502% for Cr³⁺, and 663% for Zn²⁺ compared to RH-0, determined at the initial concentration of 10 mg/L. Kinetic studies also showed rapid adsorption within the first 10–15 min, dominated initially by boundary-layer diffusion, followed by chemisorption-driven equilibrium behavior. The pseudo-second-order (PSO) model provided an excellent fit for all metals (R² = 0.999), indicating maximum model-predicted kinetic capacities of 555.56 mg/g (Cu²⁺), 769.23 mg/g (Cr³⁺), and 434.78 mg/g (Zn²⁺). Langmuir isotherms also fitted well (R² = 0.941–0.995), with predicted monolayer capacities of 535.33 mg/g (Cu²⁺), 491.64 mg/g (Cr³⁺), and 318.88 mg/g (Zn²⁺). Freundlich modeling further indicated favorable heterogeneous adsorption, with K_F values of 42.614 (Zn²⁺), 20.443 (Cr³⁺), and 16.524 (Cu²⁺) and heterogeneity factors (n) greater than 1 for all metals. These overall results suggested that gamma irradiation substantially enhanced RH functionality that enabled fast and high-capacity heavy-metal adsorption through surface oxidation and carbon valorization. Gamma-irradiated RH, therefore, represented a promising, low-cost, and environmentally friendly biosorbent for wastewater treatment applications. Full article

This study aimed to determine the nutrient use efficiency of the yacon potato under NPK fertilization at different rates. The experiment followed a randomized block design with four replications and a split-plot arrangement. The main plots consisted of three fertilization levels (60%, 100%, and 140% of the reference dose—50:80:60 kg ha⁻¹ of NPK), with subplots to data collection intervals, performed every 30 days, for a total of 7 collections, generating 21 treatments. The dry biomass of whole plants and tuberous roots was determined. Samples were taken to determine the content of N, P, K, Ca, Mg, Cu, Fe, Mn, and Zn. The biological utilization coefficient (BUC) was calculated by dividing the mean values of dry biomass in kilograms of plant parts by the kilogram of nutrient found in that biomass. The application of 100% of the reference dose led to the highest use efficiency of P, K, Ca, and Mg, and intermediate efficiency for N in yacon tuberous roots and total biomass production throughout the cycle, provides a significant contribution to fertilization planning for this crop. The amount applied which was 100% of the reference dose was 17, 80, and 20 kg ha⁻¹ of N, P₂O₅, and K₂O, respectively, at planting, supplemented with 33 and 40 kg ha⁻¹ of N and K₂O as topdressing. Full article

ZnO semiconductor-based photocatalysts are mainly studied for the elimination of toxic textile dyes. Metal-doped ZnO displays better performance for this purpose. Herein, Al-doped ZnO (Al–ZnO) was prepared using the mechanochemical calcination method with varying aluminum concentrations for the degradation of the persistent methylene blue (MB) dye. Various characterization techniques, including XRD, FTIR, FESEM, TEM, UV-DRS, and XPS, revealed the improved properties of 3% Al–ZnO in degrading the MB dye. It exhibits 96.56% degradation of 25 mg/L MB dye under 60 min of natural sunlight irradiation with a catalyst dose of 0.5 g/L at a natural pH of 6.4. A smaller particle size, a lower band gap energy of 3.264 eV, and the presence of oxygen vacancies and defect states all facilitate photocatalytic degradation. Radical scavenger experiments using ascorbic acid (for •O₂⁻), 2-propanol (for •OH), and diammonium oxalate (for h⁺) confirmed the crucial role of superoxide (•O₂⁻) and hydroxyl (•OH) radicals in the degradation mechanism. The achievement of 82.80% MB degradation efficiency at the 4th cycle validates the notable stability and excellent reusability of Al–ZnO. Full article

The challenges of glioblastoma multiforme treatment are related to limitations in tumor removal surgery, its high heterogeneity and aggressiveness, development of resistance to standard therapy, the blood–brain barrier, and the side and toxic effects of the conventional antitumor agents used in clinical practice. Although new treatment strategies continue to emerge, progress remains slow and has not resulted in substantial improvements in patient survival. The main goal of research in recent years has been aimed at developing ways to deal with all these challenges. One of the ways to improve the control of glioblastomas is the introduction of effective new antitumor agents. Metal complexes represent a particularly promising class of compounds in this context. This is why the aim of this study was to assess the effects of six homo- and heterometallic coordination compounds bearing Schiff base ligands—[Zn₂(Ampy)(µ-OH)(H₂O)₂](ClO₄)₂ (ZnAmpy), [Zn₂(Dmen)(µ-OH)(H₂O)₂](ClO₄)₂ (ZnDmen), ¹_∞[{Zn₂(Ampy)(μ₃-OH)}₂(H₂O){μ-[Au(CN)₂]}](ClO₄)₃·THF·H₂O (ZnAmpyAu), [{Zn₂(Dmen)(μ-OH)}₂{μ-[Au(CN)₂]}{[Au(CN)₂]₂}](ClO₄)·H₂O (ZnDmenAu), ¹_∞[Zn(Salampy){μ-Au(CN)₂}] (ZnSalampyAu), and ¹_∞[Zn(Saldmen)(μ-Au(CN)₂}] (ZnSaldmenAu)—on the viability and proliferation of 8MGBA and U251MG human glioblastoma multiforme cells (HDmen and HAmpy are bicompartmental Schiff base ligands resulting from the condensation of 2,6-diformyl-p-cresol with N,N-dimethylethylenediamine and 2-(aminomethyl)pyridine, respectively, while HSaldmen and HSalampy are tridentate Schiff base ligands obtained via condensation of salicylaldehyde with N,N-dimethylethylenediamine and 2-(aminomethyl)pyridine, respectively). Among these compounds, ZnSaldmenAu is a new compound and is reported here for the first time. Cytotoxicity of the compounds was evaluated through analysis of cell viability, 2D/3D growth, cytopathological alterations, and induction of cell death. The results obtained by methods with different targets in cells and the associated mechanisms of action revealed that the compounds investigated show promising cytotoxic/potential antitumor activity in treated cells. Full article

Heavy metal enrichment in agricultural soils can affect crop safety, ecosystem functioning, and long-term land productivity, yet farm-scale screening is often constrained by limited routine monitoring data. This study develops a GIS-based framework that combines field-scale spatial analysis with explainable machine learning to characterize and predict heavy metal enrichment on an intensively managed cereal farm in eastern Kazakhstan. Topsoil samples (0 to 20 cm) were collected from 34 fields across eight campaigns between 2020 and 2023, yielding 241 composite field–campaign observations for eight metals (Pb, Cu, Zn, Ni, Cr, Mo, Fe, and Mn) and routine soil properties (humus, pH in H₂O, and pH in KCl). Concentrations were generally low but spatially heterogeneous, with wide observed ranges for several elements (for example, Pb 0.06 to 2.20 mg kg⁻¹, Zn 0.38 to 7.00 mg kg⁻¹, and Mn 0.20 to 38.0 mg kg⁻¹). We synthesized multi-metal structure using an HMI defined as the unweighted mean of z-standardized metal concentrations, which supported field-level screening of persistent enrichment and emerging hot spots. We then trained Extreme Gradient Boosting models using only humus and pH predictors and evaluated performance with field-based spatial block cross-validation. Predictive skill was modest but nonzero for several targets, including HMI (mean R² = 0.20), indicating partial spatial transferability under conservative validation. SHAP analysis identified humus content and soil acidity as dominant contributors to HMI prediction. Overall, the workflow provides a transparent approach for field-scale screening of heavy metal enrichment and establishes a foundation for future integration with satellite-derived covariates for broader monitoring applications. Full article

Spinel-based glass-ceramics face challenges such as a narrow crystallization window for the target phase and the difficulty in suppressing the competitive Li_xAl_xSi_1−xO₂ crystals. This study proposes a method to regulate the phase formation in ZnO-MgO-Al₂O₃-SiO₂ glass by precisely controlling the heat treatment temperature. The microstructural evolution was analyzed by DSC, XRD, Raman spectroscopy, SEM, TEM, and XPS. The results indicate that the heat treatment at a nucleation temperature of 780 °C for 2 h and a crystallization temperature of 880 °C for 2 h effectively inhibits the precipitation of the Li_xAl_xSi_1−xO₂ secondary phase, yielding a glass-ceramic with nano-sized MgAl₂O₄, ZnAl₂O₄ spinel as the primary crystalline phase. The obtained glass-ceramic exhibits excellent mechanical properties, including a Vickers hardness of 922.6 HV, a flexural strength of 384 MPa, and an elastic modulus of 113 GPa, while maintaining a high visible light transmittance of 84.3%. This work provides a clear processing window and theoretical basis for fabricating high-performance, highly transparent spinel-based glass-ceramics through tailored heat treatment. Full article

Microparticles (MPs) are delivery systems for bioactive compounds with particle sizes in the micrometer range (1–1000 μm). This study reports a green protocol for the biosynthesis of ZnO-, MgO-, and CaO-MPs using the probiotic strains Lactobacillus delbrueckii subsp. bulgaricus, Streptococcus thermophilus, and Leuconostoc mesenteroides. Ultraviolet–visible (UV-Vis) spectroscopy, scanning electron microscopy (SEM), and dynamic light scattering (DLS) were used for the preliminary characterization of the metal oxide MPs. Antimicrobial activity was evaluated against pathogenic and phytopathogenic microorganisms, including Salmonella typhimurium, Staphylococcus aureus, Escherichia coli, and Ralstonia solanacearum. UV-Vis analysis revealed previously reported blue shifts in the ZnO- and CaO-MPs. DLS measurements showed particle sizes larger than 1000 nm in 95% of the cases, while smaller sizes were observed by SEM. The stability of the MPs, based on their zeta potential values, ranged from relatively to moderately stable. This study demonstrates that the six probiotic lactic acid bacteria strains are capable of synthesizing ZnO-MPs, CaO-MPs, and MgO-MPs. All MPs exhibited antimicrobial activity against pathogens and phytopathogens at different concentrations. Although similar antimicrobial effects have been reported for metal oxide nanoparticles produced by probiotic bacteria, considering the potential environmental and human health impacts of nanoparticles, the use of safer materials obtained through green synthesis—such as metal oxide MPs—may represent a more suitable alternative. Full article