Search Results (932)

This work develops a novel phosphate-functionalized extraction resin (HEHEHP + Cyanex272)/SiO₂-P via the vacuum impregnation method for efficient separation of light rare earth element impurities from lanthanum (La³⁺) in nitric medium through synergistic extraction. Batch experiments have demonstrated superior adsorption selectivity toward impurity ions over La³⁺ in a pH 4 nitric acid solution. Column studies confirmed exceptional performance under ambient conditions, achieving a lanthanum treatment capacity of 120.6 mg/g and over 98% impurity removal, which surpasses most reported values. Notably, this purification process enables direct production of purified La³⁺ solutions through a single-column system without desorption, significantly enhancing efficiency and reducing costs. Mechanistic insights revealed combined ion exchange and coordination interactions between metal ions and P-OH/P=O groups, corroborated by advanced characterization and density functional theory calculations. These findings indicate a higher binding affinity of light rare earth compared with La³⁺. This strategy provides a scalable approach for ultra-high-purity lanthanum compound production in advanced optical and electronic applications. Full article

RMB₆-TMB₂ (RM = rare earth elements, TM = transition metal elements) composites retain superior field emission properties of RMB₆ while addressing its inherent mechanical limitations by constructing a eutectic structure with TMB₂. Herein, an in situ route for synthesizing RMB₆-TMB₂ composite nanopowders with homogeneous phase distribution using reduction reactions was proposed. The LaB₆-ZrB₂ composite nanopowders were synthesized in situ for the first time using sodium borohydride (NaBH₄) as both a reducing agent and boron source, with lanthanum oxide (La₂O₃) and zirconium dioxide (ZrO₂) serving as metal sources. The effects of the synthesis temperature on phase compositions and microstructure of the composites were systematically investigated. The LaB₆-ZrB₂ system with a eutectic weight ratio exhibited an accelerated reaction rate, achieving a complete reaction at 1000 °C, 300 °C lower than that of single-phase ZrB₂ synthesis. The composite phases were uniformly distributed even at nanoscale. The composite powder displayed an average particle size of ~170 nm when synthesized at 1300 °C. With the benefit of the in situ synthesis method, LaB₆-TiB₂, CeB₆-ZrB₂, and CeB₆-TiB₂ composite powders were successfully synthesized. This process effectively addresses phase separation and contamination issues typically associated with traditional mixing methods, providing a scalable precursor for high-performance RMB₆-TMB₂ composites. Full article

This study investigates the nonlinear, regime-dependent, and frequency-specific interdependencies between rare earth element (REE) markets and key global critical sectors, including artificial intelligence, semiconductors, clean energy, defense, and advanced manufacturing, under varying levels of geopolitical and financial uncertainty. The main objective is to assess how REE markets transmit and absorb systemic risks across these critical domains. Using a mixed-methods approach combining Quantile-on-Quantile Regression (QQR), Continuous Wavelet Transform (CWT), and Wavelet Transform Coherence (WTC), we examine the dynamic connections between two REE proxies, SOLLIT (Solactive Rare Earth Elements Total Return) and MVREMXTR (MVIS Global Rare Earth Metals Total Return), and major sectoral indices based on a dataset of daily observations from 2018 to 2025. Our results reveal strong evidence of asymmetric, regime-specific risk transmission, with REE markets acting as systemic amplifiers during periods of extreme uncertainty and as sensitive receptors under moderate or localized geopolitical stress. High co-volatility and persistent low-frequency coherence with critical sectors, especially defense, technology, and clean energy, indicate deeply embedded structural linkages and a heightened potential for cross-sectoral contagion. These findings confirm the systemic relevance of REEs and underscore the importance of integrating critical resource exposure into global supply chain risk strategies, sector-specific stress testing, and national security frameworks. This study offers relevant insights for policymakers, risk managers, and institutional investors aiming to anticipate disruptions and strengthen resilience in critical industries. Full article

The Gabal Um Samra (GUS) compound intrusion in the Eastern Desert of Egypt consists of a co-magmatic series of syenogranite and alkali feldspar granite. Accessory minerals (e.g., zircon, monazite, allanite) are abundant. Geochemically, the GUS intrusion is a classic A-type granite. It is extensively fractionated, enriched in large ion lithophile elements and high field strength elements, and depleted in Ba, Sr, K, and Ti. Normalized rare earth element patterns are nearly flat, without any lanthanide tetrad anomalies, but with distinct negative Eu anomalies (Eu/Eu* = 0.14–0.22) due to feldspar fractionation. Paired Zr-Hf and Y-Ho element systematics indicate igneous rather than hydrothermal processes. The petrogenesis of the comparatively unaltered GUS intrusion offers an opportunity to refine the standard model for post-collisional felsic magmatism in the Neoproterozoic Arabian–Nubian Shield. It is explained by the partial melting of juvenile crust induced by lithospheric delamination, followed by extensive fractional crystallization. A quantitative mass-balance model shows that the granite varieties of the GUS intrusion plausibly represent liquids along a single liquid line of descent; but, if so, the more evolved, later pulses display anomalous enrichment in Rb, Nb, Ta, U, and REE. The most plausible source for this enrichment is the extraction of small-degree residual melts from earlier pulses and the mixing of the melts into the later pulses, an energetically favorable process we call “auto-assimilation”. A quantitative model shows that the residual liquid after 97.5% crystallization of the syenogranite can fit the major oxide and trace element data in the alkali feldspar granite if 0.07% by mass of this melt is added to the evolving system for each 1% crystal fractionation by mass. The GUS intrusion represents an example of moderate rare metal enrichment and concentration to sub-economic grade by auto-assimilation. Similar processes may affect intrusions that feature higher grade mineralization, but the evidence is often obscured by the extensive alteration of those deposits. Full article

Lanthanide/transition metal-doped luminescent materials are advanced materials with broad application potential. This type of material achieves control and optimization of luminescence performance by introducing lanthanide/transition metal ions into the host material and utilizing its unique electronic structure and optical properties. Luminescent materials are suitable for optical communication devices, biological imaging, and photodetectors. The combination of lanthanide/transition metals with various matrix materials provides a new platform for creating new chemical and physical properties in materials science and device applications. In this paper, we summarize the latest progress in the research of lanthanide/transition metal-doped luminescent materials and explain their roles in biological imaging, sensing, and optoelectronic applications. It starts with various synthesis techniques and explores how to cleverly incorporate rare earth/transition metals into various matrices, thereby endowing them with unique properties. Then, the advantages and disadvantages of each synthesis technique are discussed. Subsequently, the focus will be on functional strategies and their applications. Finally, strategies for lanthanide/transition metal ion-doped luminescent materials to address challenges are proposed, and insights from each section are summarized. Full article

This work examines the possibility of using a PbO₂-based electrode doped with the rare-earth metal holmium in the field of oxygen evolution and the development of an efficient method for the degradation of acetamiprid. Acetamiprid is a widely used insecticide and, as such, it very often reaches waterways, where it can cause many problems for wildlife and the environment. X-ray powder diffraction analysis, Raman spectroscopy, and energy-dispersive X-ray spectroscopy results confirmed the structure of Ti/SnO₂-Sb₂O₃/Ho-PbO₂, while the morphology of its surface was investigated by scanning electron microscopy with energy-dispersive X-ray spectroscopy. Ti/SnO₂-Sb₂O₃/Ho-PbO₂ showed good OER activity in alkaline media with a Tafel slope of 138 mV dec⁻¹. The Ti/SnO₂-Sb₂O₃/Ho-PbO₂ electrode shows very good efficiency in removing acetamiprid. By optimizing the degradation procedure, the following operating conditions were obtained: a current density of 20 mA cm⁻², a pH value of the supporting electrolyte (sodium sulfate) of 2, and a concentration of the supporting electrolyte of 0.035 M. After optimization, the maximum efficiency of removing acetamiprid (10 mg L⁻¹, 4.5 × 10⁻⁵ mol) from water was achieved, 96.8%, after only 90 min of treatment, which represents an efficiency of 1.125 mol cm⁻² of the electrode. Additionally, it was shown that the degradation efficiency is strictly related to the concentration of the treated substance. Full article

Syndiotactic polystyrene (sPS) is an important class of engineering plastics, primarily produced through metal-catalyzed highly stereoselective polymerization of styrene monomer. This paper summarizes the advances in metal catalysts for syndiospecific polymerization of styrene and its derivatives including mono-cyclopentadienyl titanium and rare-earth metal catalysts. The effects of the cyclopentadienyl, the metal center, and the ancillary ligand on styrene polymerization are emphasized. It provides a practical reference for polymer and organometallic chemists who are interested in developing and designing highly efficient mono-cyclopentadienyl metal catalysts for the synthesis of sPS and functionalized sPS. Full article

The endohedral metallofullerenes with a rare-earth metal encapsulated into the carbon cage are nanoparticles with potentially wide applications. We present the results of our quantum-chemical modelling of Sc@${\mathrm{C}}_{60}$, Y@${\mathrm{C}}_{60}$ and Sc₂@${\mathrm{C}}_{60}$, Y₂@${\mathrm{C}}_{60}$ endofullerenes and calculate their structures and vibrational spectra. Our calculations show that the encapsulation of an additional metal atom inside the carbon cage significantly changes the vibrational spectrum of endofullerene. The most significant changes in the far-IR (below 600 cm⁻¹) spectra are due to the metal–carbon cage vibration modes. Full article

Formo-phenolic-like resins were synthesized by replacing phenol with phloroglucinol, a biobased and biocompatible compound, and using different aldehydes, such as biomass-derived furaldehyde and glyoxal. Studies on the adsorption of rare earth elements from an aqueous organic acid solution indicate that these resins follow the Langmuir isotherm model, with maximum adsorption capacities ranging from 0.38 to 0.75 mmol/g. Adsorption was temperature-independent but strongly influenced by pH, with an up to fourfold increase between pH 2 and 5. Extraction kinetics were rapid, reaching equilibrium within two hours. Complete metal recovery was achieved within ten minutes using a 1 mol/L HCl desorption solution. Selectivity also varied with pH; glyoxal- and furfural-based resins showed superior separation performance at pH 2–3 and 3–4, respectively. The application of this method to real-world samples, including permanent magnet and red mud organic acid leachates, demonstrated effective extraction of rare earth elements and promising selectivity over iron (Fe), cobalt (Co), and nickel (Ni). Full article

Electrochemical sensors have been developed based on polyethylene terephthalate track-etched membranes (PET TeMs) modified by photograft copolymerization of N-vinylformamide (N-VFA) and trimethylolpropane trimethacrylate (TMPTMA). The modification, structure and properties of the modified PET TeMs were thoroughly characterized using scanning electron microscopy (SEM) and atomic force microscopy (AFM), thermogravimetric analysis (TGA), Fourier-transform infrared (FTIR) spectroscopy, gas permeability measurements and contact angle analysis. Optimal membrane modification was achieved using C = 10% (N-VFA), 60 min of UV irradiation and a UV lamp distance of 10 cm. Furthermore, the modified membranes were implemented in a two-electrode configuration for the determination of Eu³⁺, Gd³⁺, La³⁺ and Ce³⁺ ions via square-wave anodic stripping voltammetry (SW-ASV). The sensors exhibited a linear detection range from 10⁻⁷ M to 10⁻³ M, with limits of detection of 1.0 × 10⁻⁶ M (Eu³⁺), 6.0 × 10⁻⁶ M (Gd³⁺), 2.0 × 10⁻⁴ M (La³⁺) and 2.5 × 10⁻⁵ M (Ce³⁺). The results demonstrated a significant enhancement in electrochemical response due to the grafted PET TeMs-g-N-PVFA-TMPTMA structure, and the sensor showed practical applicability and consistent performance in detecting rare earth ions in tap water. Full article

The information on the seasonal variability of the chemical composition of the Arctic rivers is necessary for the proper assessment of the status of river runoff and the influence of anthropogenic and natural factors. Spring freshet is an especially important period for the Arctic rivers with a sharp maximum of water discharge. The Kolyma River is the least studied large river with a basin located solely in the permafrost zone. The change in the concentration of dissolved organic carbon (DOC), major, trace, and rare earth (RE) elements was studied at the peak and waning of the spring freshet of 2024 in the lower reaches of the Kolyma River. The concentration of elements was determined in filtrates <0.45 μm and in suspended solids > 0.45 μm. The content of coarse colloids (0.05–0.45 μm) was estimated by the intensity of dynamic light scattering (DLS). It was shown that the freshet peak is characterized by a minimal specific conductivity, concentration of major cations, and chemical elements migrating mainly in solution (Li, Sr, and Ba). During the freshet decline, the concentration of these elements increases with dynamics depending on the water exchange. The waters from the Kolyma River main stream have a maximal content of coarse colloids and concentration of <0.45 μm forms of hydrolysates (Al, Ti, Fe, Mn, REEs, Zr, Y, Sc, and Th), DOC, P, and heavy metals (Cu, Ni, Cd, and Co) at the freshet peak. A decrease of 8–10 times for hydrolysates and coarse colloids (0.05–0.45 μm) and of 3–6 times for heavy metals was observed at the freshet waning during the first half of June. This indicates a large-scale accumulation of easy soluble forms of hydrolysates, DOC, and heavy metals in the seasonal thawing topsoil layer on the catchment upstream in the previous summer, with a flush out of these elements at the freshet peak of the current year. In the large floodplain watercourse Panteleikha River, the change in concentration of major cations and REEs, Zr, Y, Sc, and Th at the freshet is less accented compared with the Kolyma River main stream due to a slower water exchange. Yet, <0.45 μm forms of Fe, Mn, Co, As, V, and P show an increase of 4–6 times in the Panteleikha River in the second half of June compared with the freshet peak, which indicates an additional input of these elements from the thawing floodplain landscapes and bottom sediments of floodplain watercourses. The concentration of the majority of chemical elements in suspended matter (>0.45 μm) of the Kolyma River is rather stable during the high-water period. The relative stability in the chemical composition of the suspended solids means that the content of the suspension and not its composition is the key to the share of dissolved and suspended forms of chemical elements in the Kolyma River runoff. Full article

The development of low-cost and high-efficiency oxygen evolution reaction (OER) catalysts is essential to enhance the practicality of electrochemical water splitting for green hydrogen production. Layered double hydroxides (LDHs), especially those based on nickel and cobalt, have attracted attention due to their tunable composition, abundant redox-active sites, and earth-abundant constituents. However, their application is hindered by their limited conductivity and sluggish reaction kinetics. In this study, rare-earth-element-doped NiCo LDHs were synthesized directly on nickel foam through a one-step hydrothermal approach to improve the OER activity by modulating the electronic structure and optimizing the surface morphology. Among the representative catalysts, the incorporation of Sm significantly influenced the microstructure and electronic configuration of the catalyst, as confirmed by X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). Electrochemical tests showed that the optimized Sm-NiCo LDH achieved a low overpotential of 172 mV at 10 mA cm⁻² and a small Tafel slope of 84 mV dec⁻¹ in 1 M KOH, indicating an expanded electrochemically active surface and improved charge transport. Long-term stability tests further showed its durability. These findings suggest that Sm doping enhances the OER performance by increasing active site exposure and promoting efficient charge transfer, offering a promising strategy for designing rare-earth-modified, non-precious-metal-based OER catalysts. Full article

Critical metals such as rare earth elements (REEs) are primarily associated with silicates and aluminosilicates in coal fly ash, resulting in poor REE recovery. Silicate bacteria can decompose silicate minerals and release silicon, but their impact on REE extraction remains unclear. In this study, two coal fly ash samples with different origins and combustion methods were bioleached by Paenibacillus mucilaginosus, and the effects of bio-desilication on REE leaching were examined. First, the optimal bio-desilication conditions were determined as a pulp density of 1%, an initial pH of 7.0 and an initial cell concentration OD₆₀₀ = 0.2. Compared to circulating fluidized bed (CFB) coal fly ash, silicon in pulverized coal furnace (PCF) coal fly ash was more difficult to dissolve by P. mucilaginosus. After bio-desilication, the acid leaching rate of REEs improved by 8–15% for CFB coal fly ash but only 4–5% for the PCF sample. Further investigation found that the surface turned rough and the specific surface area of coal fly ash increased after bio-desilication, which are conducive to REE extraction. Additionally, there was more quartz and mullite in PCF coal fly ash, which are more resistant to biological corrosion than amorphous silicate. The results demonstrate that bio-desilication can improve REE recovery, providing new perspectives for the low-cost green utilization of coal fly ash. Full article

Some of nuclear power’s primary detractors are the unique environmental challenges and impacts of radioactive wastes generated during fuel cycle operations. Key benefits of spent fuel reprocessing (SFR) are reductions in primary high active waste (HAW) masses, volumes, and lengths of radiotoxicity at the expense of secondary waste generation and high capital and operational costs. By employing advanced waste management and resource recovery concepts in SFR beyond the existing standard PUREX process, such as minor actinide and fission product partitioning, these challenges could be mitigated, alongside further reductions in HAW volumes, masses, and duration of radiotoxicity. This work assesses various current and proposed SFR and fuel cycle options as base cases, with further options for fission product partitioning of the high heat radionuclides (HHRs), rare earths, and platinum group metals investigated. A focus on primary waste outputs and the additional energy that could be generated by the reprocessing of high-burnup PWR fuel from Gen III(+) reactors using a simple fuel cycle model is used; the effects of 5- and 10-year spent fuel cooling times before reprocessing are explored. We demonstrate that longer cooling times are preferable in all cases except where short-lived isotope recovery may be desired, and that the partitioning of high-heat fission products (Cs and Sr) could allow for the reclassification of traditional raffinates to intermediate level waste. Highly active waste volume reductions approaching 50% vs. PUREX raffinate could be achieved in single-target partitioning of the inactive and low-activity rare earth elements, and the need for geological disposal could potentially be mitigated completely if HHRs are separated and utilised. Full article

This work investigated the ion exchange technique for selective separation of rare earth elements (REE) from acid mine drainage (AMD), using different column systems, pH values, and eluent concentrations. Systematic analysis of pH and eluent concentration showed that an initial pH of 6.0 and 0.02 mol L⁻¹ NH₄EDTA are the optimal conditions, achieving 98.4% heavy REE purity in the initial stage (0 to 10 bed volumes). This represents a 32-fold increase compared to the original AMD (6.7% heavy REE). The speciation of REE and impurities was determined by Visual Minteq 4.0 software using pH 2.0, which corresponds to the pH at the inlet of the fractionation column. Under this condition, La and Nd and the impurities (Ca, Mg, and Mn) remained in the fractionation column, while Al was partially retained. In addition, the heavy REE (Y and Dy) were mainly in the form of REE-EDTA complexes and not as free cations, which made fractionation more feasible. The fractionation column minimized impurities, retaining 100% of Ca and 67% of Al, generating a liquor concentrated in heavy REE. This sustainable approach adopted herein meets the critical needs for scalable recovery of REE from diluted effluents, representing a circular economy strategy for critical metals. Full article