Search Results (1,076)

Effects of varying lanthanum (La) content on the melting characteristics, spreadability, mechanical properties of brazed joints, and microstructure of low-silver BAg5CuZn brazing filler metal were investigated. The results indicate that the addition of La has little effect on the solidus and liquidus temperatures of the filler metal, while an excessive amount of La slightly raises its liquidus temperature. An appropriate amount of La enhances the spreadability of the filler metal on both copper and stainless steel plates and simultaneously inhibits grain growth, refining the microstructure of the BAg5CuZn-xLa filler metal. When the La content in the filler metal reaches 0.3%, the shear strength of the 304 stainless steel/304 stainless steel joint brazed with BAg5CuZn-xLa filler metal reaches 492 MPa, which is 17.7% higher than that of the brazed joint without the La addition. Full article

In the present work, polyvinylpyrrolidone (PVP) was selected as the primary raw material and fully dissolved in N,N-dimethylformamide (DMF) solvent. Hydroxymethyl cellulose (HMC), acrylic acid (AA) monomer with outstanding chelating performance, and UR were added in sequence. On this basis, composite nanofiber membrane substrates of PVP/AA/HMC/UR were fabricated by means of electrospinning. Afterwards, silane coupling agent KH-560 was blended with polylactic acid (PLA). A uniform PLA/KH-560 functional coating was covered on the surface of the as-prepared nanofiber membrane via microfluidic coating treatment, and the target composite nanofiber adsorbent was ultimately obtained. Relevant performance characterization results indicated that moderate addition of HMC could greatly optimize the tensile strength of the membrane material, whereas excessive HMC dosage would cause a deterioration in mechanical strength. Moreover, the breaking elongation presented a slight declining trend, and the integrated mechanical stability of the membrane could fully meet the service demands for cyclic reuse. As a functional monomer, acrylic acid effectively boosted the material’s adsorption performance toward typical heavy metal ions, including Zn²⁺, Cu²⁺ and Pb²⁺. In simulated acidic wastewater generated from rare earth mining and extraction (pH = 3 and pH = 6.5), the removal efficiency of the as-prepared material for the three heavy metal ions all exceeded 95%. Even after being soaked in strong acid solution at pH 2 for 8 h, its adsorption rate was still maintained at 88.5%. In the cyclic experiment, the adsorption efficiency stayed above 75% after two recycling runs, decreased to roughly 55% in the third cycle, and dropped below 30% at the fourth reuse stage. The introduction of UR imparted remarkable acid-resistant structural stability to the composite material. The membrane structure remained complete without damage after long-term immersion in a pH 2 strong acid environment, and high-efficiency heavy metal removal capability could be guaranteed when the solution pH was not lower than 3. Targeting the practical treatment dilemma of acidic heavy metal-containing wastewater from rare earth exploitation and extraction, this research successfully developed a novel eco-friendly adsorbent featuring superior acid resistance, high adsorption performance and certain recyclability. This newly designed material makes up for the deficiencies in traditional adsorbents represented by activated carbon, including poor heavy metal removal ability in acidic media and secondary pollution risks resulting from disposable use. The research findings can offer a novel technical reference and feasible approach for the purification of acidic rare earth wastewater in practical engineering applications. Full article

A series of novel heterometallic rare-earth chloroterephthalate metal–organic frameworks with the general formula (Tb_xGd_1−x)₂(Cl-1,4-bdc)₃·5H₂O (x = 0–1) were synthesized via direct precipitation from aqueous solutions. The structural and photophysical properties of these compounds were studied in detail. All compounds exhibit bright luminescence upon UV excitation into the ligand absorption band due to an efficient antenna effect. The photoluminescence quantum yield shows a non-monotonic dependence on the concentration of the terbium ion with a maximum value of 71% achieved for the compound containing equal molar fractions of the lanthanide ions. The (Tb_0.5Gd_0.5)₂(Cl-1,4-bdc)₃·5H₂O sample was evaluatedfor its utility in both qualitative and quantitative analysis of selected metal ions and in latent fingerprint development. It was shown to enable the detection of Cr(III), Fe(III), and Cu(II) ions through luminescence quenching, with the emission intensity being concentration-dependent. This behaviour highlights the compound’s potential as a basis for analytical protocols and materials aimed at the quantitative determination of these metal ions. Full article

Tungsten and tin are critical raw materials for the European Union, yet robust exploration guides for these metals remain poorly defined. The Variscan granites of the Iberian Peninsula host numerous W-Sn deposits, but the geochemical criteria that distinguish productive from barren intrusions are still debated. This study presents a comprehensive whole-rock geochemical dataset from North and Central Portugal and Castilla-León in Spain. We demonstrate that while all studied granites are peraluminous, chondrite-normalised REE patterns allow discrimination of 15 distinct geochemical groups that correlate with emplacement age and mineralisation type. Tin-specialised leucogranites (e.g., Golpejas and Enaras) are characterised by extremely low ΣREE (<40 ppm), flat patterns (La/Yb_N < 10), and absent to positive Eu anomalies, together with enrichments in Rb (>800 ppm) and Sn (>500 ppm), and very low K/Rb ratios (<70). In contrast, tungsten-bearing granites (e.g., Borralha, Valderrodrigo) exhibit moderate to high ΣREE (40–272 ppm), strongly fractionated patterns (La/Yb_N > 15), and pronounced negative Eu anomalies (Eu/Eu* < 0.4). These differences confirm that W and Sn mineralisation in NW Iberia arise from distinct magma sources and differentiation paths. This work verifies how, through their mode of occurrence and the geochemistry of rare earth elements and trace elements, potentially mineralised granites can be distinguished and how they can be used in exploration programs. Full article

Garnet-structured compounds have long been recognized as versatile host platforms for luminescent phosphors, owing to their robust chemical stability and highly tunable cationic sublattices. Conventional aluminate and gallate garnets, however, generally face intrinsic limitations, including severe concentration quenching at high dopant levels, relatively high phonon energy, and unsatisfactory efficiency for long-wavelength near-infrared (NIR) emission. In recent years, sodium-based germanate garnets, constructed by introducing aliovalent Na⁺ into dodecahedral sites combined with Ge⁴⁺ substitution in tetrahedral frameworks, have emerged as a promising branch of garnet phosphors. The aliovalent Na+ incorporation brings unique structural effects, including energy migration blocking, coordination environment distortion, and defect level modulation, which endow the materials with advantages in mitigating concentration quenching, boosting energy transfer efficiency, and enhancing thermal stability. This review systematically summarizes the crystal structure classification and luminescence fundamentals of sodium-based germanate garnet systems, and introduces mainstream synthesis techniques represented by the high-temperature solid-state method. Focusing on representative host systems, the luminescence characteristics and energy transfer mechanisms of both rare earth- and transition metal-doped systems are elaborated in detail, followed by a summary of four representative performance regulation strategies: cationic disorder engineering, crystal field engineering, defect engineering and dual-site cooperative regulation. The multifunctional applications of these materials in white light-emitting diodes, plant growth lighting, fluorescence temperature sensing, NIR imaging, and information encryption are also presented. Finally, existing challenges and future research perspectives are proposed to provide guidance for the development of high-performance garnet phosphors. Full article

This work is devoted to the description of the thermodynamics of the condensed states of the rare-earth metal europium under intense mechanical and thermal loading in shock waves. A new model of the equation of state for metallic materials is proposed based on the characteristic function of entropy with volume and internal energy (per unit mass) as variables. Within the framework of this model, calculations of the thermodynamic characteristics of europium at high pressures and specific entropies were carried out, the results of which are presented in comparison with the available data from shock-wave experiments. The developed equation of state for this material can be effectively applied to the modeling and simulation of various dynamic processes at high energy densities. Full article

Ion-imprinted polymers (IIPs) are advanced adsorbents featuring selective recognition cavities for targeted metal ion capture, offering a promising route to high-efficiency separation in extractive metallurgy. In the present work, the evolution, design principles, synthesis strategies, separation mechanisms, and practical applicability of IIPs for metal recovery from complex aqueous matrices are overviewed. Key material components, including functional monomers, crosslinkers, template ions, initiators, solvents, and support materials, are discussed in relation to adsorption capacity, selectivity, kinetics, stability, and recyclability. Major preparation routes, such as surface imprinting, bulk polymerization, in situ polymerization, and sol–gel methods, are critically compared to clarify their advantages and limitations. Recent applications for base metals, precious metals, and rare-earth elements demonstrate that IIPs can achieve high specificity and rapid equilibrium under optimized conditions. However, their translation from simulated solutions to real leachates remains constrained by interfering ions, organic contaminants, mass transfer resistance, incomplete template removal, and matrix complexity. Mitigation strategies, including sample pretreatment, improved polymer architecture, and hybrid supports, are therefore emphasized. Additionally, chemometric modelling, machine learning, or artificial intelligence-assisted design may be implemented to advance the prospects of IIPs in industry. Conclusively, IIPs represent a strong separation platform, yet industrial deployment requires robust validation with real feed streams and scalable regeneration protocols during column operation, as well as under chemically aggressive conditions at scale. Full article

Hospital wastewater has begun to act as an important source of emerging contaminants, including rare earth elements (REEs), mostly lanthanides, and radiopharmaceutical residues originating from diagnostic and therapeutic nuclear medicine procedures. The increasing use of gadolinium-based contrast agents, lutetium-containing therapeutics, technetium-99m tracers, iodine-131, yttrium-90, and gallium-68 radiopharmaceuticals has raised growing concerns regarding the release of radioactive and metal-containing compounds into aquatic environments. Conventional wastewater treatment plants are often inefficient in removing these contaminants because of their high chemical stability, low environmental concentrations, and complex aqueous speciation. In this context, hybrid nanomaterials containing silver nanoparticles (AgNPs) have attracted increasing interest for both monitoring and remediation applications. AgNP-based systems exhibit unique plasmonic, catalytic, antimicrobial, and sensing properties that can be exploited in adsorption, photocatalysis, membrane filtration, electrochemical detection, and surface-enhanced Raman spectroscopy (SERS). This review critically analyzes recent advances in hospital wastewater treatment and how hybrid nanomaterials containing silver nanoparticles (AgNPs) are emerging. The review places a particular focus on contamination by REEs and radiopharmaceuticals residues, which to date, as far as we know, remains a challenging and understudied aspect, as reflected by limited publications. Full article

The growing demand for rare earth elements (REEs), heavy metals (HMs) and precious metals (PMs) has intensified interest in sustainable recovery strategies from secondary resources, including mining residues, industrial effluents and waste electrical and electronic equipment (WEEE). These streams represent exposure interfaces, because soluble and bioavailable metal species may persist, bioaccumulate and contribute to oxidative stress, genotoxicity, carcinogenic outcomes and chronic systemic effects. This systematic review, conducted following PRISMA guidelines, evaluates the thermoacidophilic red microalga Galdieria spp. as an extremophilic platform for metal bioremediation, recovery and upstream risk reduction. Galdieria spp. combines tolerance to low pH, elevated temperature and high metal loads with rapid surface biosorption and, in living biomass, slower intracellular sequestration and detoxification. Its interaction with REEs, PMs and toxic HMs is mediated by cell-wall functional groups, extracellular polymeric substances, redox-active processes and metabolic flexibility shaped partly by horizontal gene transfer (HGT). The review discusses matrix complexity and adsorption–desorption cycles, highlighting their implications for real industrial streams. Overall, Galdieria spp. emerges as a robust extremophilic bio-interface for selective metal recovery, hazardous waste mitigation, circular-economy biorefinery models and prevention of metal-associated risks to environmental and human health, while current scale-up limitations and process-oriented research priorities are identified. Full article

Neodymium (Nd) and dysprosium (Dy) are two critical rare earth elements for fabricating NdFeB permanent magnets, which have crucial applications in modern technologies. The increasing global demand for Nd and Dy emphasizes new efficient processes for their recovery and purification, which are technologically challenging due to their close physical and chemical properties. Through systematic exploration, it was found that Lewatit VP OC 1026 resin impregnated with di-(2-ethylhexyl) phosphoric acid (D2EHPA) had a strong adsorption preference for Dy³⁺ over Nd³⁺, which is highly suitable for Dy-Nd separation from their mixed solutions under optimized conditions. The loaded resin could be eluted using dilute sulfuric solutions for recycling to the adsorption process. By employing a multistage adsorption-elution process analogous to distillation, efficient Dy-Nd separation and purification were realized from their mixed solution, with a prospective purity of 99.13% and recovery of 97.45% for Dy and a prospective purity over 99.96% and recovery of above 99.90% for Nd, despite the large concentration disparity between Dy and Nd, where Nd concentration is over 26 times that of Dy. This research demonstrates that efficient recovery and purification of metals from aqueous solutions can be achieved using selective resin adsorption processes analogous to distillation, despite large concentration differences of the metals in the solutions, which presents new alternative approaches. Full article

Ion-type rare earth tailings are mechanically weak and may release Pb and Zn, posing both geotechnical and environmental risks. Basalt-fiber-reinforced microbially induced carbonate precipitation (BF-MICP) was investigated as a combined solidification/stabilization treatment for these tailings. By integrating peak and post-peak mechanical responses, heavy-metal leaching, the spatial distribution of calcium carbonate (CaCO₃), and microstructural characterization, this study distinguishes the respective contributions of microbial mineralization and fiber reinforcement. Tailings specimens were treated with basalt fiber contents ranging from 0 to 0.8% and evaluated using unconfined compression tests, leaching tests, CaCO₃ measurements, X-ray diffraction, Fourier-transform infrared spectroscopy, and scanning electron microscopy with energy-dispersive spectroscopy. The unconfined compressive strength first increased and then decreased with increasing fiber content, reaching 1.72 MPa at 0.4% fiber, approximately 90% higher than that of the MICP-only group. At the same fiber content, compressive total energy absorption increased from approximately 18 to 68 kJ·m⁻³, indicating a marked improvement in post-peak toughness. BF-MICP treatment increased the CaCO₃ content to approximately 2–3 times that of untreated tailings, although the deposits remained more abundant in the outer region than in the core, and the total CaCO₃ content varied little with fiber dosage. The leached concentrations of Pb and Zn decreased by 79–81% and 81–84%, respectively, with no clear additional reduction as the fiber dosage increased. Microstructural analyses showed that calcite-dominated deposits connected tailing particles and fiber surfaces. These results indicate that MICP primarily governed mineral cementation and heavy-metal immobilization, whereas basalt fibers mainly improved load transfer, crack bridging, and post-peak structural integrity. A fiber content of 0.3–0.4% provided the best overall balance between mechanical performance and leaching control. Full article

Ammonia selective catalytic reduction (NH₃-SCR) has become the mainstream core technology for denitrification of industrial sintering flue gas, owing to its high denitrification efficiency and mild reaction conditions. Cerium-based catalysts, with CeO₂ as the primary component, have been identified as a promising system for replacing traditional vanadium-based and noble metal catalysts. These catalysts rely on the reversible Ce³⁺/Ce⁴⁺ redox cycle and exhibit favorable oxygen storage-release capacity derived from lattice oxygen migration. However, the presence of multiple impurities in industrial flue gas can lead to catalyst poisoning and restrict its industrial application. Consequently, there is an urgent need for the development of cerium-based catalysts that exhibit both high denitrification activity and excellent resistance to sulfur, heavy metal and water poisoning for the engineering application of NH₃-SCR technology. The present paper undertakes a systematic analysis of the poisoning mechanisms of various pollutants on cerium-based SCR denitrification catalysts. In addition, it discusses the enhancement effects of doping modification with rare earth elements, transition metal elements and non-metallic elements on the sulfur resistance of catalysts. Furthermore, it reveals the intrinsic laws of different modification pathways in improving sulfur resistance by optimizing the electronic structure, regulating surface acidic sites and inducing the formation of oxygen vacancies. The present study provides theoretical support for the design and industrial application of anti-poisoning cerium-based catalysts. Full article

Hydrogen-rich compounds under high pressure are promising for high-temperature superconductivity, but many high-$T_{\mathrm{c}}$ hydrides rely on rare-earth or alkaline-earth elements and remain difficult to tune chemically. Transition-metal hydrides offer an alternative platform because partially filled d states can modify the electronic density of states, metal–hydrogen hybridization, and electron–phonon coupling. Here, ${\mathrm{VH}}_3$ is used as a parent high-pressure transition-metal hydride framework, and Ti substitution is introduced as a chemically compatible way to tune the d-derived states near the Fermi level. Two ternary hydrides, ${\mathrm{Ti}}_3{\mathrm{VH}}_{12}$ and ${\mathrm{TiV}}_3{\mathrm{H}}_{12}$, are therefore constructed from the ${\mathrm{VH}}_3$ lattice and investigated by first-principles calculations at 200 GPa. Both compounds are thermodynamically and dynamically stable under this pressure condition, as indicated by formation energies, the Ti–V–H convex hull, and phonon spectra. Within the same ultrasoft-pseudopotential computational framework, ${\mathrm{Ti}}_3{\mathrm{VH}}_{12}$ and ${\mathrm{TiV}}_3{\mathrm{H}}_{12}$ yield Allen–Dynes $T_{\mathrm{c}}$ values of 42.1 K and 36.8 K, respectively, higher than the corresponding ${\mathrm{VH}}_3$ value. A norm-conserving cross-check for ${\mathrm{VH}}_3$ gives a different absolute value, indicating that the $T_{\mathrm{c}}$ estimates are method-dependent. Electronic structure analysis indicates that Ti incorporation shifts pronounced van Hove singularities close to the Fermi level, enhances the density of states, and changes the Fermi surface topology. These results suggest that Ti–V–H hydrides are a useful model system for examining how transition-metal substitution can couple structural stability with electronic tuning in compressed hydride superconductors. Full article

The oxygen-evolving center (OEC) in photosynthesis is a unique biological Mn₄CaO₅-cluster that splits water into electrons, protons, and dioxygen. It is a great challenge for chemists to develop a robust and precise mimic of the OEC in the laboratory. Herein, we report the formation of a rare-earth-element-containing Mn₄YO₄-cluster that represents an excellent and robust model of the OEC. The key synthetic precursor, the Mn₃YO₂-cluster, is reported for the first time, which possesses an identical mixed-valence Mn^III₂Mn^IV metal core and a hydrogen-bonding network coordination sphere. This precursor is very reactive and can convert into various compounds in solution. Importantly, it has been found that the presence of organic bases significantly influences the distribution of intermediates and promotes the formation of the Mn₄YO₄-cluster. Meanwhile, two Mn₄YO₄-clusters are described, which closely mimic the main metal-oxide core and peripheral ligands, as well as the oxidation states of the four Mn ions in the OEC, revealing that both the terminal ligands and a bridging carboxylate are variable. This new Mn₄YO₄-cluster displays a remarkable stability in the presence of water in acetonitrile solution. These findings shed new light on the synthesis of rare-earth-element-containing clusters and the rational design of robust artificial water-splitting catalysts, and provide chemical insights into the dynamic structural changes of both biological and artificial clusters. Full article

Handheld Laser-Induced Breakdown Spectrometry (hLIBS) is capable of simultaneous multi-element analysis of a variety of geological materials such as rocks, minerals, ores, soils, sediments, and water. This is a transformative analytical technology that is currently revolutionizing the field of critical mineral exploration studies. By providing real-time, in situ elemental analysis in the field with detection and quantitative determination capabilities for light elements (such as Li, Be, and B), where other handheld techniques like portable XRF struggle, hLIBS empowers geologists to make faster and more informed decisions in the field, significantly accelerating the exploration process from prospecting to target delineation. Several important practical examples of the exploration of critical metals, such as lithium, rare earth elements, copper, cobalt, and titanium, are presented. In particular, the detection capability of indicator minerals and pathfinding elements by hLIBS is extremely valuable for critical mineral exploration studies. Similar instruments have also been successfully used in recent years in challenging environments like space and deep-sea environments. The capability of remotely operated miniature LIBS in hostile environments such as the deep sea, Moon, and Mars is discussed with examples. LIBS has become a key technology for in situ chemical analysis in both space and deep-sea exploration because of its ability to identify elemental composition rapidly and without physical contact. Full article