Search Results (2,206)

Chromium (Cr) is a highly toxic heavy metal, yet its effects on soil invertebrates—particularly Caenorhabditis elegans (C. elegans)—remain insufficiently understood, especially regarding how soil properties and Cr speciation change regulate its bioavailability and toxicity. In this study, the toxicity of Cr(VI) to the growth, fertility, and reproduction of C. elegans was assessed in six representative agricultural soils following 7, 60, and 120 days of spiked soil aging, following ISO 10872 guidelines. Substantial differences in toxicity were observed among soils after 7 days of aging, with toxicity ranking from low to high as black soil < yellowish-red soil < red soil < yellow–brown soil < fluvo-aquic soil < purple soil. After 60 days of aging, Cr(VI) toxicity decreased markedly, with EC₅₀ values for growth, fertility, and reproduction increasing by 1.04–2.32, 1.04–2.34, and 1.40–2.20 times, respectively. Organic matter (OM) and amorphous aluminum oxides (Al_AO) were identified as the principal soil properties that were significantly correlated with Cr(VI) toxicity and were useful for explaining and estimating toxicity thresholds within the range of soils examined in this study. In addition, the magnitude of the aging effect showed significant positive correlations with both amorphous aluminum oxides (Al_AO) and total aluminum (Al_total), suggesting that Al-bearing minerals may contribute to the time-dependent immobilization of Cr(VI) under the experimental conditions of this study. These findings expand the ecotoxicological database for chromium, improve the prediction of toxicity thresholds under diverse soil conditions, and provide a scientific basis for refining soil environmental quality standards and developing targeted management strategies for Cr-contaminated agricultural soils. Full article

The mineral-mapping capability of three spaceborne sensors with different spatial and spectral resolutions, the Environmental Mapping and Analysis Program (EnMap), Sentinel-2, and World View-3 (WV3), is assessed regarding bauxite mining wastes in Amphissa, Greece, with validation based on ground samples. We applied the well-established Linear Spectral Unmixing (LSU) and Spectral Angle Mapping (SAM) classification techniques utilizing endmembers of two established spectral libraries and incorporated ground data through geochemical and mineralogical analyses, X-ray fluorescence (XRF), Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS), and X-ray Diffraction (XRD), to assess classification performance. The main lithologies in this area are bauxites and limestones; therefore, aluminum oxyhydroxides, calcite, and iron oxide minerals were the dominant phases as indicated by the XRF/XRD results. Almost all target minerals were mapped with the three sensors and both methods. The performance of EnMap is affected by its coarser spatial resolution despite its higher spectral resolution using these methods. Sentinel-2 is most effective for mapping iron-bearing minerals, particularly hematite, due to its higher spatial resolution and the presence of diagnostic iron oxide absorption features in the VNIR. World View 3 Shortwave Infrared (WV3-SWIR) performs better when mapping calcite, benefiting from its eight SWIR spectral bands and very high spatial resolution (3.7 m). Hematite and calcite yield the highest accuracy, especially with SAM, indicating 0.80 for Sentinel-2 (10 m) for hematite and 0.87 for WV3-SWIR (3.7 m) for calcite. AlOOH shows higher accuracy with SAM, ranging from 0.57 to 0.80 across the sensors, while LSU shows lower accuracy, ranging from 0.20 to 0.73 across the sensors. This study showcases each sensor’s ability to map minerals while also demonstrating that spectral coverage and the spatial and spectral resolution, as well as the characteristics of the selected endmembers, exert a critical influence on the accuracy of mineral mapping in mine waste. Full article

The AZ31 magnesium alloy is an attractive lightweight metallic material, but its low corrosion resistance and wear resistance significantly limit its widespread application in fields such as aerospace, the automotive industry, and mechanical engineering. Moreover, most coating systems currently cannot restore their original functions and dimensions after localized damage. Based on this, this study combined cold spray (CS), micro-arc oxidation (MAO), and magnetron sputtering (MS) to develop a high-performance and repairable composite modification strategy. First, a 5056 aluminum alloy coating was prepared on AZ31 via CS, followed by the growth of a hard alumina (Al₂O₃) coating via MAO and a diamond-like carbon (DLC) coating via MS on the 5056 aluminum alloy surface. The microstructure, phase composition, hardness, tribological properties, and electrochemical corrosion behavior of the coatings were evaluated using scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDS), X-ray diffraction (XRD), Vickers hardness testing, ball-on-disk dry sliding wear testing, and potentiodynamic polarization testing in a 3.5% sodium chloride solution. The CS 5056 aluminum alloy coating reduced the corrosion current density of AZ31 from 4.098 × 10⁻⁵ A/cm² to 2.714 × 10⁻⁶ A/cm². The MAO alumina coating increased the hardness of AZ31 from 68.60 HV_0.05 to 1614.00 HV_0.05 and decreased the wear rate from 1.703 × 10⁶ μm³/(N·m) to 2.038 × 10³ μm³/(N·m). The DLC coating further reduced the average coefficient of friction of the alumina coating from 0.48 to 0.27, decreased the wear rate to 6.979 × 10² μm³/(N·m), and lowered the corrosion current density from 3.020 × 10⁻⁶ A/cm² to 8.860 × 10⁻⁹ A/cm². This indicates that the three-phase composite coating achieves synergistic improvements in the corrosion and wear resistance of AZ31 through complementary advantages. Additionally, the thick CS aluminum alloy underlayer provides potential repairability, enabling the restoration of function and dimensions after damage without compromising the magnesium substrate. Overall, the proposed 5056Al/Al₂O₃/DLC composite coating strategy offers a reliable protective approach for AZ31 components and is expected to further expand their application fields. Full article

This study investigates pristine and doped ZnO thin films fabricated via the sol-gel technique, aiming to address efficiency challenges when used as transparent conductive oxide (TCO) layers in thin-film solar cells. ZnO was first doped with aluminum (Al), and subsequently with both Al and reduced graphene oxide (rGO), to evaluate the individual and combined effects of these dopants. The optimal pH value for the ZnO structure was initially determined, with the film produced at pH 9 exhibiting the most favorable characteristics. Al doping was then optimized at a ratio of Al/(Al + Zn) = 0.2, followed by optimization of the graphene content at 1.5 wt%. In this context, the structural, optical, and electrical properties of pristine ZnO, Al-doped ZnO (AZO), and Al and graphene co-doped ZnO (Gr:AZO) thin films were systematically investigated. These films were integrated as TCO layers into Cu₂SnS₃ (CTS)-based thin-film solar cells fabricated via physical vapor deposition (PVD). The cell architecture employed an 80 nm pristine ZnO window layer, while the doped ZnO films (300 nm) served as TCO layers. To assess the influence of the chemically deposited top layers, device performance was compared against a reference cell in which all layers were fabricated entirely using PVD. As expected, the reference cell exhibited superior performance compared to the cell whose AZO layer deposited chemically; however, the incorporation of both Al and graphene significantly enhanced the efficiency of the chemically modified cell, outperforming devices using only pristine or singly doped ZnO films. These results demonstrate the promising potential of co-doped solution-processed ZnO films as an alternative TCO layer in improving the performance of thin-film solar cell technologies. Full article

The inherent limitations of conventional polyolefin separators, particularly their poor thermal stability and insufficient mechanical strength, pose significant safety risks for lithium-ion batteries (LIBs) by increasing susceptibility to thermal runaway. In this study, we developed a novel multilayer separator through sequential coating of a commercial polyethylene (PE) substrate with aluminum oxide (Al₂O₃), para-aramid (PA), and polyethylene wax microspheres (PEWMs) using a scalable micro-gravure process, denoted as SAPEAS, signifying a PE-based asymmetric structure separator with enhanced thermal shutdown and dimensional stability. The SAPEAS separator exhibits an early thermal shutdown capability at 105 °C, maintains structural integrity with negligible shrinkage at 180 °C, and demonstrates comprehensive performance enhancements, including enhanced mechanical strength (tensile strength: 212.3 MPa; puncture strength: 0.64 kgf), excellent electrolyte wettability (contact angle: 12.8°), a high Li⁺ transference number (0.71), superior ionic conductivity (0.462 mS cm⁻¹), outperforming that of commercial PE separators. In practical LFP|Gr pouch cells with ampere-hour (Ah) level capacity, the SAPEAS separator enables exceptional cycling stability with 97.9% energy retention after 1000 cycles, while significantly improving overcharge tolerance compared to PE. This work provides an effective strategy for simultaneously improving the safety and electrochemical performance of LIBs. Full article

The present study aimed to evaluate the effect of air-abrasion as a dentin pre-treatment on the bond strength of contemporary adhesive systems. The bonding approaches included etch-and-rinse (ER), self-etch (SE) and universal (UN) adhesive systems, with the latter applied in both ER and SE modes. Twenty-eight third molars were used, each sectioned in four parts. All specimens were embedded in acrylic resin, ground with silicon carbide papers, and divided into eight experimental groups (n = 14) based on the combination of surface pre-treatment (air-abrasion or none) and adhesive approach. Subsequently, a resin cylinder was bonded to each surface following the respective treatment. Shear bond strength (SBS) was evaluated at a cross-head speed of 0.7 mm/min using a shear-testing machine (OM100 Odeme, Luzerna, Brazil). The data were analyzed with one-way ANOVA and Tukey’s post hoc test. No statistically significant increase in SBS after air-abrasion of dentin was found for any of the experimental groups (p > 0.05). Among the adhesive strategies, the ER system presented higher SBS values (32.81 ± 9.04 MPa) than the UN adhesive applied in SE mode (21.68 ± 5.85 MPa) (p < 0.05). Mixed failures were the most common failure type across all groups. In particular, 20.5% of the specimens exhibited adhesive failure, 14.3% cohesive failure within resin composite, 12.5% cohesive failure within dentin and 52.7% specimens demonstrated mixed failure types. Dentin pre-treatment with air-abrasion using 29 μm Al₂O₃ did not significantly increase the SBS of the three tested contemporary adhesive systems; however, the choice of adhesive strategies influenced the SBS outcomes. Full article

Background/Objectives: Ash made from juniper trees and added to cornmeal-based dishes may have provided calcium (Ca) to traditional Indigenous diets. Few studies have quantified the mineral content of juniper ash, including its Ca content. The objective of this study was to determine whether juniper ash could serve as a safe source of non-dairy Ca in an intervention study. Methods: Branches from two varieties of Juniper (Rocky Mountain Juniper, or Juniperus scopulorum and Eastern Red Cedar, or Juniperus virginiana) were harvested and burned to ash in a laboratory setting. Juniper ash from the southwestern U.S. available for retail purchase was used for comparison. All samples were tested for content of 10 nutritive elements (Ca, copper, iron, potassium, magnesium, manganese, sodium, phosphorus, selenium, and zinc) and 20 potentially toxic elements (silver, aluminum, arsenic, barium, beryllium, cadmium, cobalt, chromium, mercury, lithium, molybdenum, nickel, lead, antimony, tin, strontium, thallium, uranium, and vanadium) as well as n = 576 pesticide residues. Results: All samples contained both nutritive and potentially toxic elements. Each teaspoon of ash contained an average of 445 ± 141 mg Ca. However, the samples also contained lead in amounts ranging from 1.09 ppm to 15 ppm. Conclusions: Information on the nutritive and potentially toxic elemental content of juniper ash and how it may interact within a food matrix is insufficient to determine its safety as a Ca source. Further investigation is needed on the bioavailability of calcium oxide and its interaction with other dietary components to clarify the potential role of juniper ash in contemporary food patterns. Full article

This investigation has yielded a remarkably efficient metallic catalyst. Copper (Cu), cobalt (Co), and nickel (Ni) nanoparticles were concurrently deposited onto micron-sized aluminum (µAl) through a displacement reaction, resulting in the formation of [nCu+nCo+nNi]/µAl composites. The interfacial layer of the nanocomposite facilitates the creation of efficient oxygen transport pathways, significantly augmenting thermal release. In the context of the ADN/AP oxidizer, the [nCu+nCo+nNi]/µAl configuration demonstrates a substantial synergistic catalytic effect, reducing its thermal decomposition temperature by an impressive 104.1 °C. Combustion experiments have corroborated that this composite markedly enhances flame intensity, combustion temperature, and the burning rate of the ADN/AP system. The underlying thermal-oxidative mechanism was elucidated through comprehensive thermal analysis of the composite both prior to and following a heat treatment at 1100 °C. Moreover, through an integration of thermal analysis and combustion experiments, the catalytic mechanism of [nCu+nCo+nNi]/µAl on the thermolysis of ADN/AP was elucidated, and a plausible reaction pathway under thermal stimulation was proposed (e.g., ${\mathrm{NH}}_4{\mathrm{ClO}}_4+{{\mathrm{NH}}_4\mathrm{N}({\mathrm{NO}}_2)}_2\stackrel{\mathrm{Cu},\mathrm{Co},\mathrm{Ni}}{\to }{\mathrm{N}}_2+{\mathrm{H}}_2\mathrm{O}+\mathrm{HCl}+{\mathrm{O}}_2+\left[\mathrm{O}\right]$). The developed nanocomposite significantly enhances the performance of oxidizers, presenting considerable potential for a wide array of applications in solid propellants. Full article

Boron is a promising fuel, but its oxide layer impedes combustion. Alloying boron with other high-energy metals can significantly enhance its combustion performance. In this study, we sintered highly reactive lithium-containing Mg-Al-Li-B alloys using magnesium, aluminum–lithium alloy, and boron powder as raw materials. The effects of sintering temperature and holding time on the microstructure were investigated, and the combustion heat value and oxidation resistance of the alloy were tested. Results indicate that sintering temperature significantly influences phase formation: increasing temperature boosts phase content while reducing metallic phases, with 1100 °C identified as the optimal sintering temperature. Holding time had no discernible impact on the phase composition or combustion heat value of the sintered alloy. Alloying enhances material density, thereby increasing volumetric heat value. Thermal oxidation performance tests demonstrate that Li addition significantly lowers the alloy’s oxidation reaction temperature and activation energy, enhancing its reactivity. This high-heat-value, highly reactive alloy holds significant potential for application in pyrotechnics and propellants. Full article

Background: Adhesive indirect restorations have become increasingly common in daily clinical routine in most dental practices. Before etching and adhesive application, a sandblasting procedure is essential to clean and increase the microporosity of the surface. Air abrasion with aluminum oxide particles significantly improves the bond strength. However, this procedure may have some limitations, such as the presence of powder particles. Recently, the Er:YAG laser in QSP mode has been proposed for conditioning build-ups prior to adhesive cementation. The aim of this study was a retrospective analysis of adhesive indirect restoration in which build-up was conditioned or using a traditional sandblaster with alumina powder or using the Er:YAG laser in QSP mode. Methods: 187 posterior indirect adhesive restorations were cemented using two different conditioning techniques: in 96 cases (51.34%) build-up conditioning was performed using an intraoral sandblaster with alumina oxide (Microetcher CD, Kavo, Biberach, Germany); in 91 cases (48.66%) build-up conditioning was performed using the Er:YAG laser (Fotona LighWalker^®, Ljubljana, Slovenia) in QSP modality (1 W, 10 Hz, 100 mJ). The clinical efficacy of the two techniques was evaluated and compared, assessing the occurrence of complications such as debonding, fracture, secondary leakage, and hypersensitivity over time. Results: The frequency of secondary complications was very low in both groups. Only one case of debonding and one case of restoration cracking was observed in the sandblasting group, with none in the laser group (p = 0.329). Secondary caries occurred in both groups. A difference was observed in postoperative hypersensitivity: 6% in the sandblasting group and 1% in the laser group (p = 0.064). The Kaplan–Meier curves of the two conditioning techniques showed comparable survival over time (Log-rank test χ² = 2.4864/p = 0.1148). The mean follow-up was 30 months. Conclusions: The success rates of these restorations are very high if adhesive cementation steps are properly followed. Conditioning the build-up before etching is essential. Among these, the Er:YAG laser in QSP mode seems to provide excellent results in the absence of dust and smear layer. Recurrence rates of complications such as decementation, leakage, and cracking resulted in less than 1%. Furthermore, it is interesting to note that using the laser to condition the build-up appears to reduce the recurrence of post-cementation hypersensitivity. These data require confirmation through prospective clinical trials. Full article

Background: Plant citrate synthase (CSY) is involved in the iron deficiency (−Fe) response and aluminum (Al) detoxification. However, knowledge of CSY function in responding to excess iron (+Fe) or Al stress (+Al) is still limited. Methods: The CDS and promoter of GmCSY3 were isolated from soybean and bioinformatically analyzed. The GmCSY3 expression was detected by qRT-PCR and GUS assay. The growth of GmCSY3 recombinant yeast under +Fe or +Al was detected. The phenotype, CSY activity, citric acid concentration, chlorophyll content, MDA, H₂O₂, O₂⁻ contents, GST, CAT, SOD, and POD activities were examined in GmCSY3 overexpressed and RNAi-suppressed soybean chimeras under +Fe or +Al. Perls and Hematoxylin stained the roots, and the FCR activity was determined. Results: GmCSY3 was induced by +Fe or +Al, but not by −Fe. GmCSY3 enhanced yeast’s acid production and resistance to +Fe or +Al. GmCSY3 overexpression in soybean significantly enhanced CSY activity, promoted growth, alleviated oxidative damage caused by +Fe or +Al, with less free Fe³⁺ and Al³⁺, and reduced FCR activity, while GmCSY3 RNAi-suppressed showed the opposite effect. Conclusions: GmCSY3 promotes the process of citrate synthesis, chelates Fe³⁺ and Al³⁺, alleviates oxidative damage caused by +Fe or +Al, and modulates iron absorption in plants. Full article

Citrus trees are mainly cultivated in acidic soils. Excessive manganese (Mn) is the second most limiting factor for crop productivity in acidic soils after aluminum toxicity. The roles of reactive oxygen species (ROS) and methylglyoxal (MG) detoxification systems in augmented pH-mediated amelioration of excessive Mn are poorly understood. ‘Sour pummelo’ (Citrus grandis (L.) Osbeck) seedlings were exposed to nutrient solution at a Mn concentration of 500 (Mn500) or 2 (Mn2) μM and a pH of 3 (P3) or 5 (P5). The increase in pH attenuated Mn500-induced increases in ROS production and MG and malondialdehyde accumulation in roots and leaves. Additionally, the increase in pH enhanced the coordinated detoxification capability of both ROS and methylglyoxal scavenging systems in these tissues under Mn500. These findings corroborated the hypothesis that augmenting pH enhances the capability of these tissues to detoxify ROS and methylglyoxal under Mn excess. Therefore, this study provided new evidence on the roles of ROS and MG detoxification systems in the augmented pH-mediated amelioration of oxidative damage in ‘Sour pummelo’ leaves and roots caused by Mn excess, as well as a basis for correcting Mn toxicity by augmenting soil pH. Full article

Nano-aluminum (nAl), characterized by its high combustion enthalpy and enhanced reactivity, serves as a critical component in advanced energetic materials like solid propellants and micro-ignition devices. However, the atomic-scale mechanisms governing its core–shell structure evolution, oxidation dynamics, and interfacial interactions remain elusive to experimental probes due to spatiotemporal limitations. Molecular dynamics (MD) simulations, particularly the synergistic use of a ReaxFF reactive force field (for large-scale systems) and ab initio MD (for electronic-level accuracy), have emerged as a powerful tool to overcome this barrier. This review systematically delineates the oxidation mechanisms and core–shell structure regulation of nAl, with a focus on the multi-scale simulation paradigm integrating DFT, AIMD, and ReaxFF MD that directly supports nAl research. It critically examines the pivotal role of MD simulations in guiding the surface modification of nAl, elucidating combustion mechanisms at the atomic level, and designing interfaces in energetic composite systems. By synthesizing recent advances (2022–2025), this study establishes a clear structure–property relationship between microscopic features and macroscopic performance of nAl. Furthermore, it identifies prevailing challenges, including simulations under multi-physics loading, multi-scale bridging, and quantitative experiment-simulation validation that specifically affect nAl-based energetic systems. Finally, future research directions are prospected, encompassing the development of machine learning-empowered force fields tailored for nAl systems, multi-scale and multi-field coupling simulation frameworks targeting nAl applications, and closed-loop experiment-simulation systems for nAl-based energetic materials. This review aims to provide fundamental insights and a technical framework for the rational design and engineering application of nAl-based energetic materials in fields such as aerospace propulsion. Full article

Pharmaceutical contamination poses growing environmental risks, yet industrial adoption of advanced oxidation processes (AOPs) remains limited by high costs and the environmental impacts associated with specialized electrodes. This study demonstrates that unmodified aluminum electrodes achieve pharmaceutical degradation performance comparable to precious metal systems at dramatically reduced cost and carbon footprint. An aluminum-based electro-Fenton (EF) system was optimized for amlodipine (AML) removal through systematic evaluation of operational parameters. Under optimized conditions (pH 2.7, 35 mg L⁻¹ FeCl₃, 1.3 mM NaCl, 5 V), the system achieved 97% AML degradation within 15 min, following pseudo-first-order kinetics ($k=0.15$ min⁻¹). The mechanism combines hydroxyl radical oxidation with synergistic electrocoagulation resulting from anodic Al³⁺ release and cathodic Fe²⁺ regeneration. Sustainability assessment revealed exceptional performance: an energy consumption of 0.32 kWh m⁻³, a carbon footprint of 0.53 kg CO₂-eq m⁻³ (60–75% lower than conventional AOPs), and operational costs of $0.71–1.05 m⁻³. Aluminum electrodes cost 100× less than platinum alternatives, with the generated Al(OH)₃ sludge offering valorization potential. This work demonstrates that high-performance electrochemical remediation is achievable using Earth-abundant materials, providing a scalable and cost-effective alternative for pharmaceutical wastewater treatment in resource-constrained settings. Full article

Reusable enzyme carriers are valuable for proteomic workflows, yet many supports are expensive or lack robustness. This study describes the covalent immobilization of recombinant trypsin on micrometer-sized corundum particles and assesses their performance in protein digestion and antibody analysis. The corundum surface was cleaned with potassium hydroxide, silanized with 3-aminopropyltriethoxysilane and activated with glutaraldehyde. Recombinant trypsin was then attached, and the resulting imines were reduced with sodium cyanoborohydride. Aromatic amino acid analysis (AAAA) estimated an enzyme loading of approximately 1 µg/mg. Non-specific adsorption of human plasma proteins was suppressed by blocking residual aldehydes with a Tris-glycine-lysine buffer. Compared with free trypsin, immobilization shifted the temperature optimum from 50 to 60 °C and greatly improved stability in 1 M guanidinium hydrochloride. Activity remained above 80% across several reuse cycles, and storage at 4 °C preserved functionality for weeks. When applied to digesting the NISTmAb, immobilized trypsin provided peptide yields and sequence coverage comparable to soluble enzyme and outperformed it at elevated temperatures. MALDI-TOF MS analysis of Herceptin digests yielded fingerprint spectra that correctly identified the antibody and achieved >60% sequence coverage. The combination of low cost, robustness and analytical performance makes corundum-immobilized trypsin an attractive option for research and routine proteomic workflows. Full article