Search Results (345)

The effects of the gas tungsten arc (GTA) welding process on the microstructure and microhardness of two Mg-5Al-3RE and Mg-5Al-5RE experimental alloys (RE—rare earth elements) are presented. Both alloys were gravity-cast in a steel mould and GTA-welded in the same conditions. Analyses of the alloys’ microstructure were carried out by scanning electron microscopy (SEM+EDX) as well as X-ray diffraction (XRD). In as-cast conditions; both alloys were mainly composed of α-Mg; Al₁₁RE₃; and Al₁₀RE₂Mn₇ intermetallic phases. Additionally; α+γ eutectic (where γ is Al₁₂Mg₁₇) in the Mg-5Al-3RE alloy and an Al₂RE phase in the Mg-5Al-5RE material were revealed. The same phase composition was revealed for both alloys after the GTA welding process. The results of the dendrite arm size (DAS) and Vickers microhardness measurements were also described. Both welded materials exhibited an intensive size reduction of the structural constituents after GTA welding. About 75% smaller values of the dendrite arm spacing were revealed in the fusion zones of the investigated materials than in the as-cast conditions. The GTA welding process also influenced the microhardness of the experimental alloys and increased them by about 21% compared to the base metal; which was the consequence of the refinement of the structural constituents. Full article

In this study, we investigated how to design a tube furnace for the oxygen annealing of a REBa₂Cu₃O_7−x (REBCO, where RE = rare earth) superconducting joint. We confirmed the annealing temperature threshold of REBCO tape I_c degradation, which was 175C. A heat exchange model that included REBCO tape and a tube furnace was established by using this temperature as the boundary condition. At the same time, the temperature distribution of the REBCO tape in a commercial tube furnace was measured for the calibration of the heat exchange model. The feasibility and accuracy of the model were confirmed by comparing the real measurements and the simulation results. We then optimized the furnace design based on the model according to two criteria: a 20 mm length of REBCO tape should be kept at high temperatures for the oxygen annealing of REBCO joints and the length of tape at temperatures over the I_c degradation temperature should be as short as possible. The results of this furnace design investigation could help fabricate shorter REBCO superconducting joints, making the magnet more compact and decreasing the length of the Cu stabilizer layer to be removed. Full article

Rare-earth nanoparticles (RE-NPs), particularly NaYF₄:Yb³⁺,Er³⁺, have emerged as a promising class of photoluminescent probes for bioimaging and sensing applications. These nanomaterials are characterized by their ability to absorb low-energy photons and emit higher-energy photons through an upconversion luminescence process. This process can be triggered by continuous-wave (CW) light excitation, providing a unique optical feature that is not exhibited by native biomolecules. However, the application of upconversion nanoparticles (UCNPs) in bioimaging requires systematic optimization to maximize the signal and ensure biological compatibility. In this work, we synthesized hexagonal-phase UCNPs (average diameter: 29 ± 3 nm) coated with polyacrylic acid (PAA) and established the optimal conditions for imaging human erythrocytes. The best results were obtained after a 4-h incubation in 100 mM HEPES buffer, using a nanoparticle concentration of 0.01 mg/mL and a laser current intensity of 250–300 mA. Under these conditions, the UCNPs exhibited minimal cytotoxicity and were found to predominantly localize at the erythrocyte membrane periphery, indicating surface adsorption rather than internalization. Additionally, a machine learning model (Random Forest) was implemented that classified the photoluminescent signal with 80% accuracy and 83% precision, with the signal intensity identified as the most relevant feature. This study establishes a quantitative and validated protocol that balances signal strength with cell integrity, enabling robust and automated image analysis. Full article

This study explores the influence of two different synthesis methods on the sintering behavior of three novel high-entropy oxides possibly suitable for thermal barrier applications: (Ce_0.2Zr_0.2Yb_0.2Er_0.2Nd_0.2)O_2-δ, (Ce_0.2Zr_0.2Yb_0.2Er_0.2La_0.2)O_2-δ, and (Ce_0.2Nd_0.2Yb_0.2Er_0.2La_0.2)₂O_3+δ. Rare-Earth-based High-Entropy Oxides (RE-HEOs), recently known for their exceptional thermal stability and compositional flexibility, have gained increasing attention as potential candidates for many advanced technological applications. Thus, our current work focuses on the specific effects of synthesis techniques, namely co-precipitation and hydrothermal treatment, on the entropy-driven stabilization, microstructure, electrochemical properties, and sintering behavior of three novel RE-HEOs. The obtained results reveal significant differences in terms of densification yield and of the obtaining of the designed entropy-stabilized single phase depending on the adopted synthesis route, underscoring the critical role of synthesis in optimizing RE-HEOs for near-future technological applications. Full article

Tungsten heavy alloys (WHAs) are two-phase composites known for their exceptional density, strength, hardness, and ductility, making them ideal for radiation shielding, kinetic energy penetrators, and aerospace components. Due to their high melting point, WHAs are primarily processed via powder metallurgy, with liquid-phase sintering (LPS). Spark plasma sintering (SPS) and microwave sintering are emerging as advanced consolidation techniques. Recent research has focused on improving WHA performance through microstructural manipulation, alloying with elements like Fe, Co, Mo, and Re; rare earth oxides like Y₂O₃, La₂O₃, and Ce₂O₃; and employing high-entropy alloys (HEAs) as matrix phase. Additionally, additive manufacturing (AM) techniques are increasingly being used to fabricate complex WHA components. Despite their advantages, WHAs still exhibit limitations in penetration performance, primarily due to their tendency to form mushroom-like heads upon impact rather than self-sharpening. Ongoing research seeks to enhance shear localization, refine grain structure, and optimize processing methods to improve the mechanical properties and impact resistance of WHAs. Furthermore, modeling and simulation approaches are being explored to understand the mechanical behavior of WHAs. This review comprehensively overviews the above aspects and presents recent advances in WHA processing. Full article

Rare earth metal–organic frameworks (RE-MOFs) are mainly composed of rare earth ions and organic ligands, taking advantage of the strengths of both metal–organic frameworks (MOFs) and rare earth ions. Rare earth ions have the unique feature of unfilled 4f electron shells, which endows them with higher coordination numbers, unique luminescence properties, larger Stokes shifts, longer fluorescence lifetimes, and higher luminescence quantum efficiency. The MOFs combined with a variety of organic ligands can effectively guide the antenna effect to sensitize the rare earth ions and thus enhance the photon emission, making RE-MOFs a promising material in the field of fluorescent probes. In this paper, the recent advances in design principles, strategies, synthesis means, and monitoring mechanisms of RE-MOF materials for pollutant monitoring are presented. The intrinsic correlation between the luminescence performance of RE-MOFs, the detection of contaminants and the selection of organic ligands, and the adjustment of the MOF backbone structure is systematically and comprehensively discussed. Finally, the future development direction and application prospects of RE-MOF materials are summarized and discussed. Full article

Due to the similar physicochemical properties of rare earth ions, their separation presents significant challenges. In this study, acidic phosphonic chitosan (aPCS) was prepared by modifying chitosan with phosphite and formaldehyde for improving the water solubility and complexing ability of rare earth ions in acidic aqueous solutions. DFT calculations revealed that its phosphonic groups serve as preferred reaction sites, forming stable bidentate complexes with rare earth cations. The complexation abilities of aPCS and phosphorylated chitosan (PCS) for La(III) were compared at various pHs by complexation–ultrafiltration. The results showed that aPCS achieved a 97% rejection for La(III), while 70% for PCS at pH 5 and P/RE 10. Furthermore, aPCS maintained higher rejection than PCS at pH of 3 to 7. In conclusion, aPCS demonstrates excellent potential for the selective extraction and purification of rare earth ions. Full article

By performing first-principles calculations, we predicted a kind of novel ultrathin two-dimensional (2D) ferromagnet, single-atomic-layer EuN. EuN monolayer is a ferromagnetic half-metal with a large band gap of 1.69 eV; Eu ions in EuN are in the highest spin state and have large magnetic moments of 6 μB, much larger compared with the non-rare-earth (RE) metal ions. The magneto-crystalline anisotropy energy (MCE) of EuN monolayer is −3.72 meV per Eu ion, which is much higher than that of CrI₃ monolayer (0.685 meV per Cr ion); the magnetic dipolar energy (MDE) enhances magnetic anisotropy for EuN monolayer; large magnetic anisotropy energy (MAE) is beneficial to stabilizing the long-range ferromagnetic ordering. More importantly, different from many RE metal monolayers, hybridization between Eu-f and N-p orbitals induces ferromagnetism for EuN monolayer; the Curie temperature of EuN monolayer is above the liquid-nitrogen temperature (100 K). Additionally, the Curie temperature of EuN monolayer increases with increasing biaxial strain due to increased f-p hybridization. Full article

Rare earth-doped phosphate glasses have found widespread application in the field of solid-state and fiber laser technologies. Nevertheless, the fabrication of high-quality rare earth-doped phosphate glasses with minimal residual hydroxyl groups remains a significant challenge. To address this, a two-step melting process was utilized in this work to synthesize Er³⁺-Yb³⁺ co-doped phosphate glasses with low residual hydroxyl group content and improved optical quality. When re-melted under a N₂ atmosphere at 900 °C for 12 to 16 h, the hydroxyl absorption coefficient (α_-OH) decreased to ~1 cm⁻¹. The structural and compositional characteristics of the glass remained essentially unchanged throughout the re-melting process. The weak broadband absorption in the visible range and the red-shift of the ultraviolet absorption edge were attributed to the reduction in residual hydroxyl group content rather than carbon contamination. The dehydroxylation mechanism was governed by the physical diffusion of hydroxyl groups within the glass matrix. Full article

Rare-earth (RE) doping has been found to be a potent method to improve the structural, optical, electronic, and magnetic properties of ZnO, positioning it as a versatile material for future optoelectronic devices. This review herein thoroughly discusses the latest developments in RE-doped ZnO based on the role of the dopant type, concentration, synthesis method, and consequences of property modifications. The 4f electronic states of rare-earth elements create strong visible emissions, control charge carriers, and design defects. These structural changes lead to tunable bandgap energies and increased light absorption. Also, RE doping considerably enhances ZnO’s performance in electronic devices, like UV photodetectors, LEDs, TCOs, and gas sensors. Though, challenges like solubility constraints and lattice distortions at higher doping concentrations are still key challenges. Co-doping methodologies and new synthesis techniques to further optimize the incorporation of RE into ZnO matrices are also reviewed in this article. By showing a systematic comparison of different RE-doped ZnO systems, this paper sheds light on their future optoelectronic applications. The results are useful for the design of advanced ZnO-based materials with customized functionalities, which will lead to enhanced device efficiency and new photonic applications. Full article

Organometallic rare-earth complexes have attracted considerable attention in recent years due to their unique structures and exceptional magnetic properties. In this study, we report the synthesis and magnetic characteristics of a family of monopentamethylcyclopentadienyl-coordinated trinuclear rare-earth hepta-chloride clusters [(Li(THF)(Et₂O))(Cp^*RE)₃(μ-Cl)₄(μ₃-Cl)₂(μ₄-Cl)] (RE₃: RE =Y, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu; Cp* = pentamethylcyclopentadienide). These clusters were synthesized by reacting LiCp* with RECl₃ in a 1:1 molar ratio within a mixed solvent system (THF: Et₂O = 1:9), resulting in high solubility in common organic solvents such as DCM, THF, and Et₂O. Magnetic studies conducted on these paramagnetic clusters reveal the coexistence of ferromagnetic and antiferromagnetic superexchange interactions in Gd₃. Additionally, Dy₃ exhibits both ferromagnetic and antiferromagnetic intramolecular dipolar interactions. Notably, slow magnetic relaxation was observed in Dy₃ below 23 K under a zero DC applied field with an energy barrier of 125(6) cm⁻¹. Full article

Bis-(o-dipheylphosphinophenyl)amine, a tridentate (PNP) chelating ligand, and several of their Rare Earth (RE) metal complexes, [bis-(o-dipheylphosphinophenyl)amido]-RER₂, {[(C₆H₅)₂P-o-(C₆H₄)]₂NMR₂ (R = -CH₂-o-(C₆H₄)NMe₂: M = Y, 1; Nd, 2; Gd, 3;), are prepared in high yields. When activated with the strong Lewis acid MMAO-7, all these complexes exhibit catalytic activity toward the polymerization of isoprene (IP) in non-protic hydrocarbons. While the Nd complex (2) showed moderate activity and stereoselectivity, the Y and Gd complexes (1 and 3) exhibited extremely high catalytic efficiency in IP homo-polymerization, and produced polyisoprene rubber (PI) with 95% to over 99% cis-1,4 stereoselectivity and narrow polydispersity indices (<2.0). Moreover, under industrially relevant conditions, complex 3 can catalyze IP to produce ultrahigh molecular weight PI (UHMW-PI, MW up to 1200–2600 kg/mol) rubber with a very narrow polydispersity index (PDI ca. 1.1–1.6), a high-performance elastomeric material mimic of natural rubber (NR). Full article

Metal–organic frameworks (MOFs) have emerged as promising catalysts in the hydrogenation of bicyclopentadiene (DCPD) and furfural. The physical adsorption behaviors of substrate molecules and H₂ within the pore structures of MOFs significantly influence the efficacy of subsequent catalytic reactions. This study employs molecular dynamics (MD) simulations to identify the optimal temperature and pressure conditions for the adsorption of DCPD and H₂, as well as furfural and H₂, within rare-earth-element-based MOFs (RE-MOFs). By analyzing the physical adsorption characteristics of 1538 RE-MOFs, we investigate the correlation between pore structures and adsorption capabilities. This exploration has led to the identification of 10 RE-MOF structures that demonstrate superior physical adsorption performance for both DCPD and furfural. Following this initial evaluation, density functional theory (DFT) calculations were conducted to determine the chemisorption energies of H₂ molecules on these 10 selected RE-MOF structures. Notably, the structure identified as “JALLEQ_clean” exhibited the most optimal overall adsorption performance. This study elucidates the quantitative relationship between the pore structure of RE-MOFs and their physical adsorption performance, clarifying the influence of porosity parameters on adsorption capacity and highlighting the advantages of cluster-type structures in mass transfer and adsorption. The findings provide theoretical guidance for developing high-performance RE-MOF catalysts and offer new insights for the rational design of MOF-based catalytic materials. Full article

The aim of this study was to investigate the possibility of Ag nanoparticle crystallization in B₂O₃–Bi₂O₃ glass using a heat treatment method and to investigate the possible influence of the obtained nanoparticles on the emission intensity of Eu³⁺ ions. Borate–bismuth glasses with different B₂O₃:Bi₂O₃ molar ratios of 50:50, 60:40 and 70:50 with Ag and Eu³⁺ ions were successfully synthesized. The structure of the glasses was studied using XRD and FTIR methods. The XRD results exhibited a characteristic amorphous halo, confirming the absence of long-range order in the samples. The glass transition temperatures of various compositions, required to select the annealing temperature, were measured using DTA analysis. The strong maximum in the UV–Vis spectrum of the sample with the highest Bi₂O₃ content clearly indicated the presence of Ag nanoparticles in the glass. Moreover, a color change was observed for this sample, from slightly yellow to red. The presence of Ag nanoparticles was further confirmed via TEM and XPS studies. However, with a high content of Ag nanoparticles in the matrix, their positive effect on luminescence intensity was not observed. The obtained results show that B₂O₃–Bi₂O₃ glass and glass ceramics, with Ag nanoparticles and rare-earth (Re) ions, could be considered as a new phosphor for light-emitting diodes (LEDs). Full article

Bayan Obo rare earth concentrate (BOREC) is composed of bastnaesite, monazite and fluorite, which is recognized as a refractory mineral in the world. In order to solve the problems of waste gas treatment and comprehensive utilization efficiency of BOREC decomposed by the current concentrated sulfuric acid roasting method (500–700 °C), H₂SO₄-HCl mixed acid assisted by aluminum salt was used to leach out the bastnaesite, and the optimal conditions were determined as follows: c(H⁺) = 7 mol/L, c(1/2H₂SO₄):c(HCl) = 5:1, c(Al₂(SO₄)₃) = 0.25 mol/L, temperature 135 °C, liquid–solid ratio of 42:1, and reaction time 3 h. At this time, the leaching rates of concentrate and rare earth (La, Ce, Pr and Nd) were 74.08% and 71.95%, respectively, and the decomposition rate of bastnaesite was 96.83%. At the same time, the yield of calcium sulfate was 77.35% and the purity was 99.22%. Subsequently, sodium sulfate was added with m(Na₂SO₄):m(RE₂O₃) = 2.5:1, and the recovery rate of rare earth was 99.5%, and the purity of rare earth double salt product was 98.47% at a temperature of 90 °C. After most of the acid had been extracted with triethyloctanamine, sodium fluoride was added with a fluorine–aluminum ratio of 6:1, sodium carbonate was used to adjust pH = 3, and cryolite was obtained with a purity of 95.59% and an aluminum recovery rate of 99.6% at 90 °C. Since the separation of bastnaesite and monazite has been basically realized in the leaching stage, it is conducive to the docking of subsequent alkali decomposition and recovery of trisodium phosphate, realizing the comprehensive recovery of rare earth, fluorine, calcium, aluminum and phosphorus. Full article