Search Results (550)

Metal ions, including Mg(II), Ca(II), Sr(II), Co(II), Ni(II), Cu(II), Nd(III), Eu(III), and Tb(III), were investigated in binary systems alongside ampicillin at molar ratios of 1:1 and 1:2. These investigations were carried out in aqueous solutions, and the formation of complexes was verified through meticulous computational analysis. Detailed stability constants for the formed complexes and equilibrium constants for the involved reactions were meticulously determined. Furthermore, a comprehensive examination of the impact of ligand concentration on the configuration of the central metal atom’s coordination sphere was conducted. This investigation was complemented by spectroscopic measurements, which effectively confirmed the observed changes in the coordination sphere of the metal ions. Full article

Graphite has been recognized as a critical material by the United States (US), the European Union (EU), and Australia. Owing to its unique structure and properties, it is utilized in many industries and has played a key role in the clean energy sector, particularly in the lithium-ion battery (LIB) industries. With the projected increase in global graphite demand, driven by the shift to clean energy and the use of EVs, as well as the geographically concentrated production and reserves of natural graphite, interest in graphite recycling has increased, with a specific focus on using spent LIBs and other waste carbon material. Although most established and developing LIB recycling technologies are focused on cathode materials, some have started recycling graphite, with promising results. Based on the different secondary sources and recycling paths reported, hydrometallurgy-based treatment is usually employed, especially for the purification of graphite; greener alternatives are being explored, replacing HF both in lab-scale research and in industry. This offers a viable solution to resource dependency and mitigates the environmental impact associated with graphite production. These developments signal a trend toward sustainable and circular pathways for graphite recycling. Full article

Degradable fluorescent sensors present a promising portable approach for heavy metal ion detection, aiming to prevent secondary environmental pollution. Additionally, the excessive intake of ferric ions (Fe³⁺), an essential trace element for human health, poses critical health risks that urgently require effective monitoring. In this study, we developed a thermally degradable fluorescent hydrogel sensor (Eu-CDs@DPPG) based on europium-doped carbon dots (Eu-CDs). The Eu-CDs, synthesized via a hydrothermal method, exhibited selective fluorescence quenching by Fe³⁺ through the inner filter effect (IFE). Embedding Eu-CDs into the hydrogel significantly enhanced their stability and dispersibility in aqueous environments, effectively resolving issues related to aggregation and matrix interference in traditional sensing methods. The developed sensor demonstrated a broad linear detection range (0–2.5 µM), an extremely low detection limit (1.25 nM), and rapid response (<40 s). Furthermore, a smartphone-assisted LAB color analysis allowed portable, visual quantification of Fe³⁺ with a practical LOD of 6.588 nM. Importantly, the hydrogel was thermally degradable at 80 °C, thus minimizing environmental impact. The sensor’s practical applicability was validated by accurately detecting Fe³⁺ in spinach and human urine samples, achieving recoveries of 98.7–108.0% with low relative standard deviations. This work provides an efficient, portable, and sustainable sensing platform that overcomes the limitations inherent in conventional analytical methods. Full article

Food safety concerns related to pesticide residues in fruits and vegetables have increased globally, particularly in regions where monitoring programs are scarce or inconsistent. This study provides the first multi-year evaluation of pesticide contamination and associated dietary risks in Cape Verde, an African island nation increasingly reliant on imported produce. A total of 570 samples of fruits and vegetables—both locally produced and imported—were collected from major markets across the country between 2017 and 2020 and analyzed using validated multiresidue methods based on gas chromatography coupled to Ion Trap mass spectrometry (GC-IT-MS/MS), and both gas and liquid chromatography coupled to triple quadrupole tandem mass spectrometry (GC-QqQ-MS/MS and LC-QqQ-MS/MS). Residues were detected in 63.9% of fruits and 13.2% of vegetables, with imported fruits showing the highest contamination levels and diversity of compounds. Although only one sample exceeded the maximum residue limits (MRLs) set by the European Union, 80 different active substances were quantified—many of them not authorized under the current EU pesticide residue legislation. Dietary exposure was estimated using median residue levels and real consumption data from the national nutrition survey (ENCAVE 2019), enabling a refined risk assessment based on actual consumption patterns. The cumulative hazard index for the adult population was 0.416, below the toxicological threshold of concern. However, when adjusted for children aged 6–11 years—taking into account body weight and relative consumption—the cumulative index approached 1.0, suggesting a potential health risk for this vulnerable group. A limited number of compounds, including omethoate, oxamyl, imazalil, and dithiocarbamates, accounted for most of the risk. Many are banned or heavily restricted in the EU, highlighting regulatory asymmetries in global food trade. These findings underscore the urgent need for strengthened residue monitoring in Cape Verde, particularly for imported products, and support the adoption of risk-based food safety policies that consider population-specific vulnerabilities and mixture effects. The methodological framework used here can serve as a model for other low-resource countries seeking to integrate analytical data with dietary exposure in a One Health context. Full article

Co_0.95R_0.05Fe₂O₄ nanoparticles with R = La, Pr, Nd, Sm, and Eu were synthesized via an environmentally friendly sol–gel method. The prepared samples were studied using X-ray diffraction measurements (XRD), transmission electron microscopy (TEM), X-ray photoelectron microscopy (XPS), and magnetic measurements. All compounds were found to be single phases adopting a cubic Fd-3m structure. EDS analysis confirmed the presence of Co, Fe, R, and oxygen in all cases. The XPS measurements reveal that the Co 2p core-level spectra are characteristic for Co³⁺ ions, as indicated by the 2p_3/2 and 2p_1/2 binding energies and spin–orbit splitting values. The analysis of the Fe 2p core-level spectra reveals the presence of both Fe³⁺ and Fe²⁺ ions in the investigated samples. The doped samples exhibit lower saturation magnetizations than the pristine sample. Very good agreement with the saturation magnetization values was obtained if we assumed that the light rare-earth ions occupy octahedral sites and their magnetic moments align parallel to those of the 3d transition metal ions. The ZFC-FC curves indicate that some nanoparticles remain superparamagnetic, while others exhibit ferrimagnetic ordering at room temperature, suggesting the presence of interparticle interactions. The M_r/M_s ratio at room temperature reflects the dominance of magnetostatic interactions. Full article

Incorporation of lanthanide (Ln) and actinide (An) ions into the human body poses significant chemotoxic and radiotoxic risks, necessitating effective decorporation strategies. This study investigates the displacement of biologically relevant ligands from trivalent ions of europium, Eu(III), and curium, Cm(III), in artificial biofluids by various complexing agents, i.e., ethylenediaminetetraacetic acid (EDTA), ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid (EGTA), diethylenetriaminepentaacetic acid (DTPA), and spermine-based hydroxypyridonate chelator 3,4,3-LI(1,2-HOPO) (HOPO). Utilizing a modified unified bioaccessibility method (UBM) to simulate gastrointestinal conditions, we conducted concentration-dependent displacement experiments at both room and body temperatures. Time-resolved laser-induced fluorescence spectroscopy (TRLFS) supported by ²H nuclear magnetic resonance (NMR) spectroscopy and thermodynamic modelling revealed the complexation efficacy of the agents under physiological conditions. Results demonstrate that high affinity, governed by complex stability constants and ligand pK_a values, is critical to overcome cation and anion competition and leads to effective decorporation. Additionally, there is evidence that cyclic ligands are inferior to linear ligands for this application. HOPO and DTPA exhibited superior displacement efficacy, particularly in the complete gastrointestinal tract simulation. This study highlights the utility of in vitro workflows for evaluating decorporation agents and emphasizes the need for ligands with optimal binding characteristics for enhanced chelation therapies. Full article

As global climate change intensifies and the transition to clean energy accelerates, lithium-ion batteries—critical components of electric vehicles—are becoming increasingly vital in international trade networks. This study investigates the structural evolution and determinants of the electric vehicle lithium-ion battery trade network among European Union (EU) member states from 2012 to 2023, employing social network analysis and the multiple regression quadratic assignment procedure method. The findings demonstrate the transformation of the network from a centralized and loosely connected structure, with Germany as the dominant hub, to a more interconnected and decentralized system in which Poland and Hungary emerge as the leading players. Key network metrics, such as the density, clustering coefficients, and average path lengths, reveal increased regional trade connectivity and enhanced supply chain efficiency. The analysis identifies geographic and economic proximity, logistics performance, labor cost differentials, energy resource availability, and venture capital investment as significant drivers of trade flows, highlighting the interaction among spatial, economic, and infrastructural factors in shaping the network. Based on these findings, this study underscores the need for targeted policy measures to support Central and Eastern European countries, including investment in logistics infrastructure, technological innovation, and regional cooperation initiatives, to strengthen their integration into the supply chain and bolster their export capacity. Furthermore, fostering balanced inter-regional collaborations is essential in building a resilient trade network. Continued investment in transportation infrastructure and innovation is recommended to sustain the EU’s competitive advantage in the global electric vehicle lithium-ion battery supply chain. Full article

Electric passenger vehicles are set to dominate the European car market, driven by EU climate policies and the 2035 ban on internal combustion engine production. This study assesses the sustainability of this transition, focusing on global warming potential and Critical Raw Material (CRM) extraction throughout its life cycle. The intensive use of CRMs raises environmental, economic, social, and geopolitical concerns. These materials are scarce and are concentrated in a few politically sensitive regions, leaving the EU highly dependent on external suppliers. The extraction, transport, and refining of CRMs and battery production are high-emission processes that contribute to climate change and pose risks to ecosystems and human health. A Life Cycle Assessment (LCA) was conducted, using OpenLCA software and the Ecoinvent 3.10 database, comparing a Peugeot 308 in its diesel and electric versions. This study adopts a cradle-to-grave approach, analyzing three phases: production, utilization, and end-of-life treatment. Key indicators included Global Warming Potential (GWP100) and Abiotic Resource Depletion Potential (ADP) to assess CO₂ emissions and mineral resource consumption. Technological advancements could mitigate mineral depletion concerns. Li-ion battery recycling is still underdeveloped, but has high recovery potential, with the sector expected to expand significantly. Moreover, repurposing used Li-ion batteries for stationary energy storage in renewable energy systems can extend their lifespan by over a decade, decreasing the demand for new batteries. Such innovations underscore the potential for a more sustainable electric vehicle industry. Full article

Late Paleozoic to Early Mesozoic granitoids in the East Kunlun Orogenic Belt (EKOB) provide critical insights into the complex and debated relationship between Paleo–Tethyan magmatism and tectonics. This study presents integrated bulk-rock geochemical and zircon isotopic data for the Xingshugou monzogranite (MG) to address these controversies. LA-ICP-MS zircon U-Pb dating constrains the emplacement age of the MG to 247.1 ± 1.5 Ma. The MG exhibits a peraluminous and low Na₂O A₂-type granite affinity, characterized by high K₂O (4.69–6.80 wt.%) and Zr + Nb + Ce + Y (>350 ppm) concentrations, coupled with high Y/Nb (>1.2) and A/CNK ratios (1.54–2.46). It also displays low FeO^T, MnO, TiO₂, P₂O₅, and Mg^# values (26–49), alongside pronounced negative Eu anomalies (Eu/Eu* = 0.37–0.49) and moderately fractionated rare earth element (REE) patterns ((La/Yb)_N = 3.30–5.11). The MG exhibits enrichment in light rare earth elements (LREEs) and large ion lithophile elements (LILEs; such as Sr and Ba), and depletion in high field strength elements (HFSEs; such as Nb, Ta, and Ti), collectively indicating an arc magmatic affinity. Zircon saturation temperatures (T_Zr = 868–934 °C) and geochemical discriminators suggest that the MG was generated under high-temperature, low-pressure, relatively dry conditions. Combined with positive zircon ε_Hf(t) (1.8 to 4.7) values, it is suggested that the MG was derived from partial melting of juvenile crust. Synthesizing regional data, this study suggests that the Xingshugou MG was formed in an extensional tectonic setting triggered by slab rollback of the Paleo-Tethys Oceanic slab. Full article

Gadolinium-based contrast agents (GBCAs) are the gold standard as MRI probes but are nowadays facing medical limitations and environmental concerns. To address these issues, novel strategies focus on the optimization of Gd(III)-based probes. One promising approach involves incorporating Gd(III) into nanoparticles, particularly coordination polymers, which offer improved relaxivity. In this study, we explore the self-assembly of Gd(III) ions with ascorbate ligand, forming extended coordination polymer architectures. Our investigation focuses on understanding the impact of nanoparticles’ growth and aggregation on their relaxivity properties. Notably, the controlled aggregation process leads to a different distribution of the Gd(III) in the surface and in the bulk of the nanoparticles, mainly responsible for their longitudinal relaxivity. Additionally, the introduction of Eu(III) into the network enables the development of a dual-modal probe with paramagnetic and optical features. Full article

The recycling of lithium-ion batteries is picking up rather slowly, although recent rapid growth in consumption and increasing prevalence of battery electric vehicles have increased the quantity of recoverable material from past years of production. Yet, the diversity of different product types i.e., chemistries and product life spans complicates the recovery of raw materials. At present, large-scale industrial recycling of lithium-ion batteries employs (1) pyrometallurgy, with downstream hydrometallurgy for recovery of refined metals/salts; and (2) hydrometallurgy, requiring upstream mechanical shredding of cells and/or modules. Regulatory requirements, especially in Europe, and the high industry concentration along the lithium-ion battery value chain drive recycling efforts forward. The present study aims to quantify the potential contribution of 2nd lithium from recycling to battery production on a global and European scale up to 2050. The overall recycling output of lithium in any given year depends on the interactions between several different factors, including past production, battery lifetime distributions, and recovery rates, all of which are uncertain. The simplest way to propagate input uncertainties to the final results is to use Monte Carlo-type simulations. Calculations were done separately for EVs and portable batteries. The overall supply of lithium from recycling is the sum of the contributions from EVs and portable electronics from both the EU and the RoW in each battery production scenario. Results show a total global supply of recycled lithium below 20% in each scenario until 2050. On the EU level, the contribution of recycled lithium may reach up to 50% due to the high collection and recovery rate targets. Full article

The Late Paleozoic granitoids widely distributed in the central section of the East Kunlun Orogenic Belt (EKOB) are responsible for the constraints on its post-collisional extensional processes. We report the whole-rock geochemical compositions, zircon U-Pb ages, and zircon Hf isotope data of granites in the western Kendewula area. The granites, dated between 413.7 Ma and 417.7 Ma, indicate emplacement during the Early Devonian period. The granite is characterized by high silicon content (72.45–78.96 wt%), high and alkali content (7.59–9.35 wt%), high 10,000 × Ga/Al values, and low Al2O3 (11.29–13.32 wt%), CaO (0.07–0.31 wt%), and MgO contents (0.16–0.94 wt%). The rocks exhibit enrichment in large-ion lithophile element (LILE) content and high-field-strength element (HFSE) content, in addition to strong losses, showing significant depletion in Ba, Sr, P and Eu. These geochemical characteristics correspond to A2-type granites. The values of Rb/N and Ba/La and the higher zircon saturation temperature (800~900 °C) indicate that the magma source is mainly crustal, with the participation of mantle materials, although limited. In addition, the zircon εHf(t) values (−4.3–3.69) also support this view. In summary, the A2-type granite exposed in the western Kendewula region formed against a post-collisional extensional setting background, suggesting that the Southern Kunlun Terrane (SKT) entered a post-orogenic extensional phase in the evolution stage since the Early Devonian. The upwelling of the asthenospheric mantle of the crust, triggered by crustal detachment and partial melting, likely contributed to the flare-up of A2-type granite during this period. By studying the nature of granite produced during orogeny, the evolution process of the formation of orogenic belts is discussed, and our understanding of orogenic is enhanced. Full article

Rare earth elements (REEs) are critical mineral resources that play a pivotal role in modern technology and industry. Currently, the global supply of light rare earth elements (LREEs) remains adequate. However, the supply of heavy rare earth elements (HREEs) is associated with substantial risks due to their limited availability. Ion-adsorption type rare earth deposits (IAREDs), which represent the predominant source of HREEs, have become a focal point for exploration activities, with a notable increase in global interest in recent years. This study systematically collected stream sediments and stream water samples from the Jiaping IARED in Guangxi, as well as from adjacent granitic and carbonate background areas, to investigate the exploration significance of geochemical surveys for IAREDs. Additionally, mineralized soil layers, non-mineralized soil layers, and bedrock samples from the weathering crust of the Jiaping deposit were analyzed. The results indicate that stream sediments originating from the Jiaping IARED and granite-hosted background regions display substantially elevated REE concentrations relative to those from carbonate-hosted background areas. Moreover, δEu values in stream sediments can serve as an effective indicator for differentiating weathering products derived from granitic and carbonate lithologies. Within the mining area, three coarse-grained fractions of stream sediments (i.e., +20 mesh, 20–60 mesh, and 60–150 mesh) exhibit REE concentrations comparable to those observed in both granite-hosted and carbonate-hosted background regions. However, the HREEs content in the finer -150-mesh stream sediments from Jiaping IARED is markedly higher than that in the two background regions. The (La/Sm)_N versus (La/Yb)_N ratios of -150-mesh stream sediments in the Jiaping IARED may reflect the mixing processes involving HREE-enriched ore layer, non-mineralized layer, and LREE-enriched ore layer. This observation implies that fine-grained (-150-mesh) stream sediments can partially inherit the REE characteristics of mineralized layers within IAREDs. Scanning electron microscopy (SEM) observations indicate that the enrichment of REEs in fine-grained stream sediments primarily originates from REE-rich accessory minerals derived from parent rocks and mineralized weathering crusts. A comparative analysis reveals that the concentrations of REEs in stream water collected during the rainy season are significantly higher than those collected during the dry season. Moreover, the levels of REEs, especially HREE, in stream water from the Jiaping IARED substantially exceed those in background areas. Collectively, these findings suggest that the geochemical signatures of REEs in rainy season stream water possess diagnostic potential for identifying IAREDs. In conclusion, the integrated application of geochemical surveys of stream water and -150-mesh stream sediments can effectively delineate exploration targets for IAREDs. Full article

The attributes of Late Paleozoic magmatic events are of paramount significance in elucidating the tectonic evolution of the Ulanhot region, which is located in the middle of the Hegenshan–Heihe tectonic belt (HHTB). This study undertook a comprehensive investigation of the petrography, LA–ICP–MS zircon U–Pb dating, whole rock geochemistry, and zircon Hf isotopes of the Early Carboniferous volcanic rocks. The volcanic rocks are predominantly composed of andesite, schist (which protolith is rhyolitic tuff), and rhyolitic tuff. The results of zircon U–Pb dating reveal that the formation ages of volcanic rocks are Early Carboniferous (343–347.4 Ma). Geochemical characteristics indicate that the andesites possess a comparatively elevated concentration of Al₂O₃, alongside diminished levels of MgO and TiO₂, belonging to the high-K calc-alkaline series. The zircon εHf(t) of the andesites range from −13 to 9.4, while the two-stage Hf model ages span from 697 to 1937 Ma. The felsic volcanic rocks have high contents of SiO₂ and Na₂O + K₂O, low contents of MgO and TiO₂, and belong to high-K to normal calc-alkaline series. The zircon εHf(t) values of the felsic volcanic rocks range from −12.8 to 10, while the two-stage Hf model ages span from 693 to 2158 Ma. The Early Carboniferous volcanic rocks exhibit a notable enrichment in large ion lithophile elements (LILEs, such as Rb, K, Ba) and light rare earth elements (LREEs), depletion in high-field-strength elements (HFSEs, including Nb, Ta, Ti, Hf), as well as heavy rare earth elements (HREEs). The distribution patterns of the rare earth elements (REEs) demonstrate a conspicuous right-leaning tendency, accompanied by weak negative Eu anomalies. These characteristics indicate that the andesites represent products of multistage mixing and interaction between crustal and mantle materials in a subduction zone setting. The felsic volcanic rocks originated from the partial melting of crustal materials. Early Carboniferous igneous rocks formed in a volcanic arc setting are characteristic of an active continental margin. The identification of Early Carboniferous arc volcanic rocks in the Central Great Xing’an Range suggests that this region was under the subduction background of the oceanic plate subduction before the collision and amalgamation of the Erguna–Xing’an Block and the Songnen Block in the Early Carboniferous. Full article

This study reports the synthesis and characterization of four novel rare earth-gallic acid complexes, Sm(Gal)₃·4H₂O, Eu(Gal)₃·4H₂O, Tb(Gal)₃·4H₂O, and Dy(Gal)₃·4H₂O. These complexes were synthesized under optimized conditions (60 °C, pH 4–5) and characterized using the Ln³⁺ elemental content method, infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), mass spectrometry (MS), and fluorescence spectroscopy. IR spectra confirmed the coordination of rare earth ions (Ln³⁺) with gallic acid through carboxylate oxygen atoms. TGA revealed the thermal decomposition pathways, while MS identified the molecular ion peaks and fragmentation patterns. All complexes exhibited strong luminescence under UV excitation, with emission peaks corresponding to characteristic transitions of Sm³⁺, Eu³⁺, Tb³⁺, and Dy³⁺. Biological assays demonstrated significant antimicrobial activity against Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa, with Dy(Gal)₃·4H₂O showing the highest efficacy. Additionally, the complexes displayed inhibitory effects on MCF7 breast cancer cells, with Tb(Gal)₃·4H₂O exhibiting the lowest IC₅₀ value (11.3 µM). These findings suggest that rare earth metal complexes with gallic acid have potential applications in biomedical fields, particularly as antimicrobial and anticancer agents. Full article