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In this study, we report the synthesis of a new cubic neodymium-rhenium metallic alloy NdRe2 through the utilization of high pressure and laser heating in a diamond anvil cell. NdRe2 crystallizes in the … space group with a lattice parameter equal to 7.486 (2) Å and Z = 8 at 24 (1) GPa and 2,200 (100) K. It was studied using high-pressure single-crystal X-ray diffraction. The compound crystallizes in the cubic MgCu2 structure type. Its successful synthesis further proves that high-pressure high-temperature conditions can be used to obtain alloys holding a Laves phase structure. Ab initio calculations were done to predict the mechanical properties of the material. We also discuss the usage of extreme conditions to synthesize and study materials present in the nuclear waste. [ABSTRACT FROM AUTHOR]

A rare earth oxyborate crystal K2Nd2O(BO3)2 has been grown by means of high temperature solution method for the first time. It crystallizes in monoclinic P21/c (No. 14) space group, and the lattice parameters are a=11.318(6) Å, b=6.575(4) Å, c=10.689(6) Å, β=117.062(12)°, and Z=4. The absorption spectrum, emission spectrum, and fluorescence lifetime of K2Nd2O(BO3)2 have been evaluated, and the foundational spectral parameters have been analysed according to the Judd‐Ofelt theory. The high concentration of activated ions (1.13×1022 ions/cm3), large absorption coefficient (87.63 cm−1), long fluorescence lifetime (91.2 μs), and large emission cross section (2.03×10−20 cm2) of K2Nd2O(BO3)2 suggest its potential applications of microchip lasers. [ABSTRACT FROM AUTHOR]

A rare earth oxyborate crystal K2Nd2O(BO3)2 has been grown by means of high temperature solution method for the first time. It crystallizes in monoclinic P21/c (No. 14) space group, and the lattice parameters are a=11.318(6) Å, b=6.575(4) Å, c=10.689(6) Å, β=117.062(12)°, and Z=4. The absorption spectrum, emission spectrum, and fluorescence lifetime of K2Nd2O(BO3)2 have been evaluated, and the foundational spectral parameters have been analysed according to the Judd‐Ofelt theory. The high concentration of activated ions (1.13×1022 ions/cm3), large absorption coefficient (87.63 cm−1), long fluorescence lifetime (91.2 μs), and large emission cross section (2.03×10−20 cm2) of K2Nd2O(BO3)2 suggest its potential applications of microchip lasers. [ABSTRACT FROM AUTHOR]

Rare earth elements (REEs) are critical in modern electronics, yet sustainable, effective recovery technologies for REEs are scarce. Herein, we develop a sustainable and cost-effective neodymium (Nd) extraction technology from electronic waste using a carboxylate functionalized nanocellulose (CFNC). We demonstrate a solution-processed synthesis of CFNC from a cost-effective, readily available cellulose precursor without harsh conditions or complicated procedures. We show that Nd precipitates as Nd-CFNC complex, which can be easily separated from the solution by centrifugation. As low as 150 ppm of Nd3+ concentration is sufficient to form the precipitate instantaneously. We observe the removal of ~252 ± 5 mg of Nd3+ per gram of CFNC, which, to our knowledge, provides the highest removal capacity at the shortest contact time of a few seconds. We explore the effect of ionic strength, pH, and temperature on the performance of CFNC. As a real-time application, we demonstrate Nd recovery from a NdFeB magnet present in waste electronic equipment. The removal using CFNC is speedy, efficient, and selective. Solar-driven electrodeposition is used to recover Nd/Nd2O3. We envision that our material will provide a low-cost, promising, sustainable technology for removing other RREs from e-waste, mines, and industrial wastewater. [ABSTRACT FROM AUTHOR]

Five Nd3+-doped bismuth based alumino-phosphate glass samples are prepared by melting the raw materials. Luminescent and radiative properties of the samples are studied to find their suitability in lasing applications. The effect of chemical composition on spectroscopic properties has also been studied. Nine bands owing to transitions from 4I9/2 level to various higher levels of Nd3+-ion are observed in absorption spectroscopy. J–O parameters are observed to be influenced by the local structure of rare-earth ions. An intense emission band assigned to the transition 4F3/2 → 4I11/2 is observed on exciting the samples with 808 nm and its intensity varies as a function of concentration of Nd2O3. Stimulated emission cross-section σem(λ) and absorption cross-section σabs(λ)of transition 4F3/2 → 4I11/2 have also been examined using Fuchtbauer-Ladenburg equation and McCumber theory respectively. Large values of transition probability, high branching ratio and high stimulated cross-section of the transition 4F3/2 → 4I11/2 in comparison to previously reported Nd3+- doped similar phosphate glasses indicate its potential use in IR lasers. Luminescence intensity is maximum for GNdP(0.5) and GNdP(1.0) glass samples. Quenching of luminescence is observed on increasing the mole % of Nd2O3 beyond 1.0. The samples are further investigated for their up-conversion tendency by comparing excitation spectrum and absorption spectrum in the wavelength range 700–900 nm. Intense emission bands observed at 290 nm and 870 nm on exciting the samples at 582 and 585 nm respectively, confirms simultaneous up and down conversion in synthesized glass samples which makes them potentially useful in developing solar cells encapsulations, bio-imaging and display devices, and lasers. [ABSTRACT FROM AUTHOR]

The push to decarbonize has spurred the demand for clean energy technologies such as electric vehicles (EVs) and wind turbines (WTs). These technologies rely on rare earth permanent magnets (REPMs), namely Neodymium-Iron-Boron (NdFeB) magnets that in turn rely on rare earth elements (REEs), including Neodymium (Nd), and Dysprosium (Dy). As the demand for clean energy technologies increases, so will the demand for Nd and Dy-containing REPMs. Both Nd and Dy are critical elements that are prone to supply chain risks. As our reliance on them increases, it becomes essential to anticipate future market dynamics for these elements. This paper aims to address the current gap in the literature in the context of forecasting future Nd and Dy demand quantities. The Bass Diffusion Model is a widely used approach to forecast the adoption of new products or technologies and, to predict demand trends. Over the years, the model has found applicability in a wide variety of sectors including consumer durables, medical services, and agricultural innovations. This paper demonstrates the use of the Bass Diffusion Model to estimate future global Nd and Dy demands, enabling a better understanding of swiftly evolving clean energy technology and REPM-related market dynamics. [ABSTRACT FROM AUTHOR]

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The work presents the study results of the determination of the resistance of neodymium zirconate doped with MgO and Y2O5 to radiation damage stemming from irradiation with heavy ions akin to nuclear fuel fission fragments. The attraction towards this type of ceramics stems from its potential to raise the operational temperatures within the core of next-generation nuclear reactors. This is owed to its superior thermal conductivity when compared to zirconium dioxide, coupled with the heightened strength parameters that signify the ceramics' resistance against external factors. The main results of this study are to determine the influence of the formation of substitution or interstitial phases when adding magnesium and yttrium oxides to the composition, on increasing the stability of the strength and thermophysical parameters of neodymium zirconate to the radiation defects accumulation in the damaged surface layer. During the studies, it was found that the formation of impurity phases in the form of MgO inclusions (when it is added to the composition) and a substitution phase of the Y2Zr2O7 type (with the addition of Y2O5) results in an elevation in the hardness and crack resistance stability of neodymium zirconate ceramics, which indicates the positive effect of doping linked to the formation of additional interphase boundaries that prevent strain embrittlement of the damaged layer under high-dose irradiation. During determination of the thermophysical parameters of the studied neodymium zirconate ceramics, it was observed that the formation of interphase boundaries during doping not only enhances thermal conductivity but also mitigates the decline in the thermal conductivity coefficient during irradiation for two-phase ceramics in comparison with undoped neodymium zirconate ceramics. [ABSTRACT FROM AUTHOR]

The goals of this work are to design and develop a technology for fabrication and study of multifunctional properties of core/shell nanoparticles (NPs) as magnetic/luminescent markers. The new hybrid core/shell Fe3O4/Gd2O3:1% Er3+, 18% Yb3+, 2.5% Mg2+, x% Nd3+ NPs doped with different concentrations of neodymium ions, where x = 0%, 0.5%, 0.75%, 1%, 2%, 4%, were synthesized by the co-precipitation method. The NPs were characterised using XRD, TEM, SEM, EDX, confocal microscopy and photoluminescence. Fe3O4 (core) consists of several 13 nm NPs. The core/shell NPs have sizes from 220 nm to 641 nm. In this latter case, the shell thicknesses were 72, 80, and 121 nm. The upconversion efficiency properties and magnetic properties of the hybrid NPs were investigated. In the core/shell NPs, the addition of Nd3+ quenches the luminescence. The magnetic response of core/shell samples is rather paramagnetic and does not differ significantly from that registered for the shell material alone. For Gd2O³:1% Er3+, 18% Yb3+ and Fe3O4/Gd2O3:1% Er3+, 18% Yb3+, 2.5% Mg2+, 0.5% Nd3+, at 300 K, the values of the magnetization registered at ~ 40 kOe are similar and equal to ~ 5.3 emu·g-1. The survivability of the HeLa tumor cells with the presence of the core/shell NPs was investigated for 24 h. The NPs are non-toxic up to a concentration of 1000 µg·ml-1 and penetrate cells in the process of endocytosis which has been confirmed by confocal microscope studies. [ABSTRACT FROM AUTHOR]

The synthetic difficulty of target‐specific lanthanide complexes, despite their unique characteristics, limits their use in in vitro/ in vivo studies and biomedical applications. With commercially available and affordable reagents, a facile synthetic approach is developed to modularly deploy nitrobenzoxadiazole and neodymium complexes onto bioactive peptides. The yielded probes show observable neodymium emission with specific localization to corresponding biotargets in vitro, which became the first example of a stable, water‐soluble, and target‐specific neodymium(III) complex applicable for in vitro imaging with detectable brightness. [ABSTRACT FROM AUTHOR]

This paper reports synthesis by wet chemical route for neodymium doped lanthanum arsenates nanoparticles with chemical formula NdxLa1−xAsO4 (x = 0.0, 0.05, 0.10 and 0.15) and its characterization. Powder X-ray diffraction (PXRD) confirms monoclinic structure of the prepared nanomaterials. Crystallite size decreases with increasing concentration of Nd3+ ions. PXRD results are further validated by Rietveld refinement with low values of goodness factor (χ2). Morphology has been investigated by high resolution transmission electron microscopy (HRTEM) equipped with selected area electron diffraction (SAED) which shows the crystalline nature of nanomaterials. Various functional groups present have been studied by FTIR spectroscopy. The optical band gap calculated using UV–Vis diffuse reflectance spectroscopy is found to decrease with increasing dopant concentration. The emission spectrum studied by applying photoluminescence (PL) spectroscopy. At 315 nm excitation, the NdxLa1−xAsO4 exhibits a bright red emission with emission peaks in the range of 610–630 nm. Chromaticity plot shows that chromaticity coordinates are located in the red region. The dielectric analysis carried out to study variation of dielectric constant with frequency over range of 1–25 kHz and temperature range of 20–200 °C. The conductivity measurements are carried out and activation energy has been calculated. The variation of electrical modulus with frequency has also been observed. [ABSTRACT FROM AUTHOR]

Copyright of Electroplating & Finishing is the property of Electroplating & Finishing Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Abstract Molten oxide electrolysis is a promising pathway to decarbonize primary metal production. The oxide electrolyte is less hazardous and eco‐toxic than halides (molten salt electrolysis) and, with the use of renewably generated electricity and an inert anode, oxygen is produced as a by‐product instead of CO2. Building fundamental understanding of electrolytic operating windows requires starting with simple chemistries. Here we investigate a simplified binary oxide system as an electrolyte for titanium oxide reduction to metal. The TiO2−Na2O binary system forms a eutectic, reducing the liquidus temperature over a wide composition range. FactSage 8.1 predictions suggested Ti reduction would become favorable over Na reduction for compositions greater than 0.49 mole fraction TiO2. The prediction was validated by the detection of metallic Ti after electrolysis experiments. However, the reduction efficiency was too low (0.24±0.08 % at −0.1 V vs Ti reference electrode) for the TiO2−Na2O system to be a viable industrial electrolyte for Ti production. Scoping for other binary oxide systems was performed for electrolytic production of two critical metals, tantalum and neodymium. Based on TiO2−Na2O system's predicted behavior, candidate binary oxide systems were identified that contained congruently melting line compounds flanked by eutectic reactions from the ACerS‐NIST Phase Equilibria diagrams database.

Faraday’s law of electromagnetic induction is one of the four Maxwell’s equations, presented here in vector notation. Its discovery paved the way for a second industrial revolution based on machines powered by electricity. Roughly speaking, it states that the negative (a Lenz‘s contribution) of the temporal rate of change of magnetic fields acts as a source for an electric field of rotational nature. In this paper, we discuss readily replicable experiments demonstrating Faraday’s law in action, using the motion of a neodymium magnet under three natural motions: i) free fall under gravity; ii) pendular motion under gravity and iii) the magnet placed at the free end of a vibrating ruler. Due to their simplicity, these systems allow for a complete theoretical treatment. We consider more than one way of calculating the induced voltage in a circular coil, by the magnet in motion. This way, students can benefit from the multidisciplinary aspects, connecting the knowledge of kinematics of motion and the electrodynamics of particles in motion. The experimental data was obtained using an oscilloscope and contrasted to the theoretical predictions. In practice, these experiments can be used to estimate the magnetic dipole moment of a permanent magnet.

The tetrakis complex of neodymium(III), tetrakis{μ-N-[bis(pyrrolidin-1-yl)phosphoryl]acetamidato}bis(propan-2-ol)neodymiumsodium propan-2-ol monosolvate, [NaNd(C10H16Cl3N3O2)4(C3H8O)2]·C3H8O or NaNdPyr4(i-PrOH)2·i-PrOH, with the amide type CAPh ligand bis(N,N-tetramethylene)(trichloroacetyl)phosphoric acid triamide (HPyr), has been synthesized, crystallized and characterized by X-ray diffraction. The complex does not have the tetrakis(CAPh)lanthanide anion, which is typical for ester-type CAPh-based coordination compounds. Instead, the NdO8 polyhedron is formed by one oxygen atom of a 2-propanol molecule and seven oxygen atoms of CAPh ligands in the title compound. Three CAPh ligands are coordinated in a bidentate chelating manner to the NdIII ion and simultaneously binding the sodium cation by μ2-bridging PO and CO groups while the fourth CAPh ligand is coordinated to the sodium cation in a bidentate chelating manner and, due to the μ2-bridging function of the PO group, also binds the neodymium ion.

The Nd-mediated coordinative chain transfer polymerization (CCTP) of dienes represents one of the state-of-the-art techniques in the current synthetic rubber field. Besides having well-controlled polymerization behaviors as well as high atom economies, it also allows for the generation of highly reactive Al-capped polydienyl chain-ends, which hold great potential, yet much less explored up to date, in achieving end functionalization to mimic the structure of natural rubber. In this study, we demonstrate an efficient in situ method to realize end-functionalizing polyisoprene by introducing epoxide compounds into a CCTP system. The end functionalization efficiency was 92.7%, and the obtained polymers were systematically characterized by 1H NMR, 1H,1H-COSY NMR, DOSY NMR, and MALDI TOF. NMR studies revealed that a maximum of two EO units were introduced to the chain ends, and based on density functional theory (DFT) studies, an energy barrier of 33.3 kcal/mol was required to be overcome to open the ring of the EO monomer. Increasing the ratio of [Ip]/[Nd] resulted in gradually increased viscosities for the reaction medium and therefore gave rise to an end functionalization efficiency that decreased from 92.7% to 74.2%. The end hydroxyl group can also be readily converted to other functionalities, as confirmed by NMR spectroscopy.

The realization of single-photon generation is important for implementing various quantum information technologies. The use of rare-earth ions in an optical fiber is a promising single-photon generation method due to its ability to operate at room temperature as well as the low cost involved. Neodymium ions are especially interesting because the ions are one of the most commercially affordable rare-earth materials in the current industry. The neodymium ion also has the advantage of having a rich energy level structure, which offers several possible wavelengths for emitted single photons from visible to near-telecommunication wavelengths. In this paper, we experimentally demonstrated single-photon generation using an isolated single neodymium ion in tapered silica fiber at room temperature. Our results have significant implications as a platform for low-cost wavelength-selectable single-photon sources and photonic quantum applications. [ABSTRACT FROM AUTHOR]

In this study, Nd x :(La 0.05 Lu 0.05 Gd 0.05 Y 0.05)Ca 0.8-x F 2.2+x (x = 0.0–0.012) high-entropy transparent ceramics were prepared by the vacuum hot pressing method. The crystal structure, microstructure, elemental distribution and spectral properties of Nd x :(La 0.05 Lu 0.05 Gd 0.05 Y 0.05)Ca 0.8-x F 2.2+x , as well as the impact of Nd3+ content on these properties was systematically examined. The material demonstrates high optical transparency, achieving a maximum on-line transmittance of nearly 90 % at 1200 nm, which is very close to the theoretical CaF 2 transmittance (92%–94 %). Porosity and grain size are identified as the primary scattering factors. The EDX analysis revealed that the prepared transparent ceramics exhibited a high level of density and uniform distribution of elements. The highest luminescence intensity is observed at a Nd3+ concentration of 1 at.%, the fluorescence lifetime decays relatively slowly with increasing concentration of doped Nd3+ ions. [ABSTRACT FROM AUTHOR]

High photon energy vacuum ultraviolet radiation (VUV, 100−200 nm wavelength) is challenging to detect. It easily degrades conventional silicon and semiconductor photodetectors. Fluoride photodetectors can be the answer, but the correlation between fabrication parameters and photodetector performance is not known. Here, the effect of annealing is investigated on the characteristics of neodymium trifluoride thin film/quartz substrate interface and NdF3 photoconductivity within the VUV. Thin films are deposited on unheated and heated (600 °C) substrates with post‐deposition annealing. Dark current of films on unheated substrates decreases by as much as 1/10 as resistance increases from 1 −12 TΩ after annealing. Dark current of films on heated substrates increases even after annealing, resulting in similar photo and dark currents of ≈303.7 nA and poor detectors. Fluorine diffuses from the film to the substrate during deposition, exacerbated by substrate heating but not by annealing. Fluorine diffusion degrades crystallinity near the interface, increasing the dark current. Fluorine diffusion is absent when MgF2 is used as the heated substrate. Unannealed NdF3/MgF2 detector on 600 °C‐heated substrate and 600 °C‐annealed NdF3/SiO2 detector on unheated substrate exhibit similar resistances of ≈14 TΩ. Considering the film/substrate interface and annealing is crucial when developing VUV photodetectors. [ABSTRACT FROM AUTHOR]

There is a growing need to develop new strategies for rare earth element (REE) recovery from secondary resources. Herein, a novel approach to utilize biogenic silica (from rice husk) and metakaolin was employed to fabricate magnetic geopolymer (MGP) by incorporating metallic iron. The fabricated MGP adsorbent material was used to uptake Ce3+, La3+, and Nd3+ from synthetic solutions and real phosphogypsum leachate in batch and column modes. The MGP offers a negatively charged surface at pH above 2.7, and the uptake of REEs rises from pH 3 to 6. The kinetic study validated that the kinetics was much faster for Nd3+, followed by La3+ and Ce3+. A thermodynamic investigation validated the exothermic nature of the adsorption process for all selected REEs. The desorption experiment using 2 mol L−1 H2SO4 as the eluent demonstrated approximately 100% desorption of REEs from the adsorbent. After six adsorption–desorption cycles, the MGP maintained a high adsorption performance up to cycle five before suffering a significant decrease in performance in cycle six. The effectiveness of MGP was also assessed for its applicability in recovering numerous REEs (La3+, Ce3+, Pr3+, Sm3+, and Nd3+) from real leachate from phosphogypsum wastes, and the highest recovery was achieved for Nd3+ (95.03%) followed by Ce3+ (86.33%). The operation was also feasible in the column presenting suitable values of the length of the mass transfer zone. The findings of this investigation indicate that MGP adsorbent prepared via a simple route has the potential for the recovery of REEs from synthetic and real samples in both batch and continuous operations modes. [ABSTRACT FROM AUTHOR]

There are still challenges in the preparation of difunctional stereoregular polydienes, especially for the construction of initiating chain‐end functionalization. Coordinative chain transfer polymerization (CCTP) provides a way to achieve the goal but usually requires sophisticated functionalized catalysts as well as expensive chain transfer agents (CTAs). In this work, heteroleptic aluminum with oligo(dienyl) substituents (oligo‐Al agents) were readily prepared by living anionic polymerization (LAP) technique. The oligo‐Al agents used in Nd‐mediated CCTPs of dienes exhibit highly selective alkylation and transalkylation features. Kinetics and transfer efficiency studies using 1H NMR, 13C NMR, 1H‐13C HSQC, and Dosy NMR analyses revealed that the resulting polydienes possess substituents at the initiating chain‐end that have transferred from the oligo‐Al agents. The functionalization efficiency of the initiating chain‐end is up to 99 %, and the molar mass regulation efficiency of heteroleptic aluminum is higher than that of the traditional CTA AliBu2H (0.608 vs. 0.410). Based on the experimental results and density functional theory (DFT) calculations, we propose a mechanism in which allylic‐Al acts as an efficient alkylating moiety in catalyst preformation and also as an effective transfer agent in polymerization. Taking advantage of these features, di‐functionalized polyisoprene, polybutadiene, and poly(isoprene‐co‐butadiene) can be facilely synthesized. [ABSTRACT FROM AUTHOR]

[Display omitted] Osteosarcoma is one of the most dangerous forms of tumors, leading to death in >90% of patients. The surgical treatment of osteosarcoma results in significant bone defects and risks of tumor recurrence. Using neodymium (Nd) and manganese (Mn) ions co-doped with whitlockite nanoparticle (Nd 10% Mn 10% WH NPs) and sodium alginate (SA), we designed and synthesized an organic–inorganic composite hydrogel (Nd 10% Mn 10% WH-SA) that displayed the excellent fluorescence and photothermal properties. Furthermore, the maximum fluorescence emission intensity of Nd 10% Mn 10% WH-SA at 1062 nm was linear with temperature. The optimal temperature for the treatment of tumors was determined by considering the changes in fluorescence intensity that led to a reduction in tissue damage around the tumors. Nd 10% Mn 10% WH NPs demonstrated a significant function in promoting human bone marrow mesenchymal stem cells (hBMSCs) proliferation. Furthermore, Nd 10% Mn 10% WH-SA could almost kill tumors when the photothermal temperature was raised to 50 °C, with a minimal leftover scar after photothermal therapy (PTT). Nd 10% Mn 10% WH-SA had a better promotion effect on the growth of the new bone. These results suggested that Nd 10% Mn 10% WH-SA offers a new PTT method for the "integrated treatment and repair" of osteosarcoma. [ABSTRACT FROM AUTHOR]

The neodymium borate Nd3B5O11(OH)2 was obtained from Nd2O3, B2O3, and H3BO3 by high‐pressure/high‐temperature synthesis at 13 GPa and 850 °C. Based on single‐crystal diffraction data, a crystal structure in the orthorhombic space group Pnna (no. 52) with the unit cell parameters a=4.5128(1) Å, b=13.3264(3) Å, c=14.1882(4) Å, and four formula units per cell was found. The crystal structure is built up by a framework of corner‐sharing [BO4]5− tetrahedra forming corrugated eight‐, ten‐, and fourteen‐membered rings. Furthermore, the powder X‐ray diffraction pattern and the infrared spectrum of the title compound are reported. [ABSTRACT FROM AUTHOR]

The neodymium borate Nd3B5O11(OH)2 was obtained from Nd2O3, B2O3, and H3BO3 by high‐pressure/high‐temperature synthesis at 13 GPa and 850 °C. Based on single‐crystal diffraction data, a crystal structure in the orthorhombic space group Pnna (no. 52) with the unit cell parameters a=4.5128(1) Å, b=13.3264(3) Å, c=14.1882(4) Å, and four formula units per cell was found. The crystal structure is built up by a framework of corner‐sharing [BO4]5− tetrahedra forming corrugated eight‐, ten‐, and fourteen‐membered rings. Furthermore, the powder X‐ray diffraction pattern and the infrared spectrum of the title compound are reported. [ABSTRACT FROM AUTHOR]

The paper considers Sr, Nd, and Pb isotope data obtained for two cores of bottom sediments taken in the Oga and Tsivolki bays of Severny Island of the Novaya Zemlya archipelago. The studied sequence of sediments from Oga Bay has accumulated over the last thousand years. The 87Sr/86Sr ratio decreases from top to bottom down the section from 0.72225 to 0.71995, the value of εNd varies from –6.1 to –5.5. The Pb isotopic composition varies within narrow limits: the 206Pb/204Pb ratio from 19.107 to 19.139, the 207Pb/204Pb ratio from 15.632 to 15.635, and the 208Pb/204Pb ratio from 38.568 to 38.635. A rapid decrease in the 87Sr/86Sr ratio at a relatively stable neodymium and lead isotope composition indicates a change in the source of the clastic material. This can be explained by the fact that the material of the destruction of Permian clay shales, and then Devonian–Silurian sedimentary carbonates, first entered the area of glacier abrasion and further, respectively, into the sedimentation zone. The sediment column from Tsivolki Bay was formed over a little more than 10 000 years. Based on the Sr, Nd, and Pb isotope ratios, these bottom sediments are divided into lower and upper parts: before and after 150 cm (or ~3500 years). In the lower part of the column, the 87Sr/86Sr ratio increases from 0.72055 to 0.72580, the value of εNd remains approximately the same and varies around –8.2. In the upper part, the 87Sr/86Sr ratio drops to 0.72049 in the near-surface layer; at the same time, the value of εNd increases to –6.4. At the boundary of these two units, the 206Pb/204Pb ratio abruptly changes from about 18.0 in the lower part to 19.3 in the upper part and 208Pb/204Pb from about 36.5 in the lower part to 38.7 in the upper part of the section. The change in the Sr, Nd, and Pb isotope characteristics is likely a reflection of changes in the composition of the rocks in the area where the basin was removed, which is now being eroded by the glacier. Comparison with modern sources supplying clastic material to the Kara Sea showed that the material is supplied to the Oga and Tsivolki bays only from Novaya Zemlya. [ABSTRACT FROM AUTHOR]

In this work, solid-liquid extraction of lanthanum and neodymium ions by column technique from concentrated phosphoric acid solutions using the strongly acidic cation exchange resin was experimentally investigated. Measurements of breakthrough curves were measured as a function of column bed depth, initial metal concentration in the feed solution and flow rate. It was found that the breakthrough and time increased with the increase in bed depth and the total mass adsorbed by La(III) and Nd(III) increased with increasing bed depth. At higher initial metal concentrations, the column is quickly saturated, resulting in shorter breakthrough and exhaustion time. It was observed that with increasing the initial metal concentration from 0.10 to 0.50 g/L, the equilibrium adsorption capacities increase from 9.68 to 27.45 mg/g for La(III) and from 4.57 to 19.43 mg/g for Nd(III). Breakthrough time reaching saturation was increased significantly with a decrease in the flow rate. As the flow rate increased from 1.0 to 4.0 ml/min, the exhaustion time of La(III) and Nd(III) decreased from 135.0 to 40.0 min and from 90.0 to 35.0 min, respectively. The capacity of La(III) and Nd(III) was found to be 33.55 and 17.30 mg/g, respectively. The experimental sorption capacity and the time required for 50% adsorbate breakthrough (τ) are close to those calculated resulting from the Thomas and Yoon-Nelson model. These results indicate that the experimental data obey the Thomas and Yoon-Nelson model. [ABSTRACT FROM AUTHOR]

The aim of this work was to synthesize and investigate the roentgenographic and electro-physical properties of new phases, namely double tellurites of neodymium. Oxotellurites of the composition NdMeIITeO4.5 MeII - Ca, Ba) were synthesized by the method of ceramic technology with high-temperature interaction of Nd2O3, TeO2 oxides with carbonates of alkaline earth metals in the interval of 800°C - 1200°C . Roentgenograms of the synthesized compounds were obtained using an Empyrean powder diffractometer by PANalytical and indication was determined using the X'Pert HighScore Plus program. It was found that the synthesized tellurites were crystallized in tetragonal syngony. The unit cell parameters, roentgen and pycnometric densities of the compounds were determined. It was revealed that with increasing ionic radii from Ca to Ba, the lattice parameters and unit cell volumes of synthesized tellurites increase. The assumed structure of the synthesized double tellurites of neodymium is a distorted perovskite structure. A study of the temperature dependence of the dielectric permittivity and electrical resistance of tellurites of neodymium-alkaline earth metals established that they can possess semiconducting properties at 293 K - 483 K. Temperature coefficients of resistance and forbidden zone width of tellurites were calculated. [ABSTRACT FROM AUTHOR]

BACKGROUND: Cadmium ions may be discarded to the environment with living organisms from fossil fuel combustion, phosphate fertilizer and battery industries. It is urgent and essential to develop a sensitive and rapid method for monitoring Cd2+ level in aquatic environments and biological systems. Neodymium vanadate possesses good catalytic performance for the electrocatalysis of heavy metal ions. Single crystalline Nd vanadate nanoribbons were obtained by a facile approach and used as electrode materials for electrochemical detection of Cd2+. RESULTS: The Nd nanoribbons with tetragonal NdVO4 phase possess length, width and thickness of longer than 10 μm, 200 nm to 1.5 μm and 50 nm, respectively. Nd vanadate nanoribbons can serve as a good electron transfer interface. An anodic peak is located at +0.56 V at the Nd vanadate nanoribbon‐modified electrode in 0.1 mol L−1 KCl electrolyte containing 1 mmol L−1 Cd2+ by square wave voltammetry technique. The Nd vanadate nanoribbon‐modified electrode exhibits a linear range of 0.01–1000 μmol L−1 and a detection limit of 0.29 nmol L−1, with good stability, reproducibility and selectivity for Cd2+ detection. CONCLUSION: The optimal measurement conditions including the pH value of the KCl solution, deposition time, deposition potential and standing time, which are pH 1, 180 s, −1.0 V and 60 s, respectively. The Nd vanadate nanoribbon‐modified electrode shows great application potential for detecting heavy metal ions in liquid environments. © 2023 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

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This paper studied some equilibria in the Nd3+–water–nitric acid–TODGA (N,N,N,N-tetraoctyl diglycolamide)–CO2 system and the efficiency of extraction of Nd3+ ions from aqueous solutions into the supercritical (SC) CO2 phase at 313–353 K and 18.0–40.0 MPa. It was shown that, in the absence of TODGA, Nd3+ ions do not pass into the SC phase. The extraction efficiency increases with decreasing temperature and with increasing nitric acid concentration CNA in the aqueous solution. At 313 K, CNA > 1.5 mol/L, TODGA content not less than 100 mol/g-at. Nd, and CO2pressure ensuring complete dissolution of TODGA (19.0 MPa), Nd3+ completely pass into the SC phase. With increasing content of neodymium ions in the system, the pressure and amount of CO2 required for complete dissolution of TODGA increase. This is likely to be due to a decrease in the intensity of intermolecular interactions in the SC phase during the passage of polar Nd complexes with TODGA and nitrate ions into it. [ABSTRACT FROM AUTHOR]

In this study, all-inorganic perovskite quantum dots (QDs) for pure blue emission are explored for full-color displays. We prepared CsPbBr3 and Cs3NdCl6 QDs via hot injection methods and mixed in various ratios at room temperature for color blending. Nd-doped CsPb(Cl/Br)3 QDs showed a blueshift in emission, and the photoluminescence quantum yields (PLQY, ΦPL) were lower in the 460–470 nm range due to surface halogen and Cs vacancies. To address this, we introduced a silane molecule, APTMS, via a ligand exchange process, effectively repairing these vacancies and enhancing Nd doping into the lattice. This modification promotes the PLQY to 94% at 466 nm. Furthermore, combining these QDs with [1]Benzothieno[3,2-b][1]benzothiophene (BTBT), a conjugated small-molecule semiconductor, in a composite film reduced PLQY loss caused by FRET in solid-state QD films. This approach achieved a wide color gamut of 124% National Television System Committee (NTSC), using a UV LED backlight and RGB perovskite QDs in a BTBT-based organic matrix as the color conversion layer. Significantly, the photostability of this composite was enhanced when used as a color conversion layer (CCL) under blue-LED excitation. [ABSTRACT FROM AUTHOR]

Two neodymium sulfate based purely inorganic networks, [NH4][Nd(SO4)2(H2O)3] ⋅ H2O (1) and [Nd2(SO4)3(H2O)4] ⋅ H2O (2) have been synthesized at different reaction temperatures and pH values. The structure of 1 features a two‐dimensional (2D) anionic corrugated sheet with an sql topological net built up by linking NdO8 units and μ2‐SO42− anions, in which the NH4+ charge‐compensating/templating cations occupy the intersheet layers. While 2 possesses a 3D neutral framework with an unprecedented (3,42,7‐c) net constructed by NdO9 units and μ4‐ and μ6‐SO42− linkers. They exhibit thermally induced irreversible structural transformation associated with the dehydration and the changes in coordination geometry and dimensionality. Both compound 1 and 2 display typical antiferromagnetic interactions between the Nd3+ centres. In addition, the CO2 adsorption isotherms of the desolvated samples 1 and 2 were also investigated. [ABSTRACT FROM AUTHOR]

This paper presents the new geochemical isotope (Sr–Nd system, H2O, Cl) data obtained for basalt glasses of the Mid-Atlantic Ridge (MAR) sampled from six areas of the MAR axial zone between 31° and 12° N. The data are consistent with the existing ideas about large-scale geochemical segmentation of the MAR. It is shown that samples from predominantly serpentinite segments have a narrower range of variations of strontium isotopic composition (87Sr/86Sr = 0.7027–0.7032) in comparison with samples collected from the areas where the crustal section is dominated by basalts (87Sr/86Sr = 0.7024–0.7041). The variation ranges of the neodymium isotopic composition in these two groups of samples are almost identical (εNd = +4.9 to +10.9 and +5.9 to +11.6 in serpentinite and basalt segments, respectively), although, in general, serpentinite segments have a slightly more enriched composition. The wide variations of the neodymium isotopic composition and increased contents of Cl, H2O, and U, as well as increased K2O/TiO2 and La/Sm ratios, in samples from serpentinites can most probably be related to the participation of different geochemically heterogeneous sources in the magmatism of the MAR axial zone. The influence of enriched plume-type matter cannot be excluded in some segments. The isotopic composition of noble gases may shed light on the subject. [ABSTRACT FROM AUTHOR]

A 71-year-old female presented with progressive dysphagia and unexplained weight loss. Computed tomography and esophagogastroduodenoscopy (EGD) revealed invasive esophageal squamous cell carcinoma, which was initially treated with local radiation and esophageal stenting. Over the next year, the patient experienced multiple symptoms and hospital admissions consistent with a malignant tracheoesophageal fistula, despite negative findings on imaging, bronchoscopy, and EGD. Prophylactic antibiotics were initiated based on symptomatology to prevent septic episodes. Stent erosion into the membranous trachea was eventually observed. Neodymium-yttrium-aluminum-garnet laser bronchoscopy was used periodically to debulk the invading tumor around the stent. A percutaneous endoscopic gastrostomy tube was also inserted to facilitate enteral nutrition and avoid aspiration pneumonia. The patient reported significant improvements in respiratory symptoms following each laser debridement and has progressed well beyond the life expectancy associated with malignant tracheoesophageal fistula. [ABSTRACT FROM AUTHOR]

The tetra­kis complex of neodymium(III), tetra­kis­{μ-N-[bis­(pyrrolidin-1-yl)phos­phor­yl]acet­am­id­ato}bis(pro­pan-2-ol)neodymiumsodium pro­pan-2-ol monosol­vate, [NaNd(C10H16Cl3N3O2)4(C3H8O)2]·C3H8O or NaNdPyr4(i-PrOH)2·i-PrOH, with the amide type CAPh ligand bis(N,N-tetra­methylene)(tri­chloro­acetyl)phos­phoric acid tri­amide (HPyr), has been synthesized, crystallized and characterized by X-ray diffraction. The complex does not have the tetra­kis­(CAPh)lanthanide anion, which is typical for ester-type CAPh-based coordin­ation compounds. Instead, the NdO8 polyhedron is formed by one oxygen atom of a 2-propanol mol­ecule and seven oxygen atoms of CAPh ligands in the title compound. Three CAPh ligands are coordinated in a bidentate chelating manner to the NdIII ion and simultaneously binding the sodium cation by μ2-bridging PO and CO groups while the fourth CAPh ligand is coordinated to the sodium cation in a bidentate chelating manner and, due to the μ2-bridging function of the PO group, also binds the neodymium ion. [ABSTRACT FROM AUTHOR]

Experimental measurements were made to assess the electrical conductivity as a function of temperature and NdF3 concentration (0–20 mol %) of molten systems of (LiF–CaF2)eut–NdF3, (LiF–NaF)eut–NdF3, (NaF–CaF2)eut–NdF3 and (LiF–MgF2)eut–NdF3. The experiment used an altering current impedance spectroscopy technique with a platinum–rhodium electrode positioned in a pyrolytic BN tube and graphite a crucible/counter electrode. The conductivity of all systems under study increased with rising temperatures and decreasing NdF3 concentrations. The Arrhenius equation and linear regression have both been used to describe the experimental data. The results of the ionic conductivity for the temperature 850 °C and NdF3 concentrations 0, 10 and 15 mol %, respectively, can be compared as follows: the conductivity of the molten system of (LiF–CaF2)eut–NdF3 was determined to be 6.10, 5.95 and 5.10 S.cm−1, the results for the system (LiF–NaF)eut–NdF3 were 6.16, 5.56 and 4.13 S.cm−1, the results for the system (NaF–CaF2)eut–NdF3 were 3.78, 3.56 and 2.32 S.cm−1, and finally, the results for the system (LiF–MgF2)eut–NdF3 were determined to be for the same temperature as 5.35, 4.79 and 4.14 S.cm−1, respectively. [ABSTRACT FROM AUTHOR]

There is an immediate demand for eco-friendly, high-performance, and highly stable energy storage materials for pulse power systems. Ceramics based on SrTiO3 have a high breakdown strength (BDS) and dielectric constant. In this work, we fabricated a polycrystalline of Sr(1-x)(Nd, Li)xTiO3 ceramics via microwave-assisted heating of the starting materials. X-ray diffraction analysis reveals a pure perovskite phase without any secondary phase. Scanning electron microscopy images exhibit dense grain morphology with a decrease in grain size as the dopant concentration increases. The frequency dependences of the dielectric properties were studied in the frequency range of 100 Hz-1 MHz at room temperature. The polarization-electric field hysteresis loops were examined to ascertain the effect of co-doping on the energy-storage capability of SrTiO3 ceramics. After increasing the co-dopants from 0 to 8%, the energy density increased nine times (from 0.11 J/cm3 to 0.952 J/cm3), and the energy storage efficiency increased from 80.71% to 95.98%, respectively. In addition, the samples demonstrate excellent thermal stability, and their energy storage properties are stable up to 80°C. We may infer from this discovery that the bulk Nd3+ and Li+ co-doped SrTiO3 materials are good candidates for high-energy-density capacitor applications. [ABSTRACT FROM AUTHOR]

Perovskite solar cells have attained high photoconversion efficiencies by changing chemical compositions of the perovskites and layered structures of the devices. However, the perovskite compounds easily decompose in air atmosphere even at the room temperature, and the photovoltaic properties are degraded by the formed defects. The motivation of this work is to solve these instability problems, and the objective the present work is to improve the film quality of the perovskite compounds by introducing lanthanide elements and decaphenylcyclopentasilane (DPPS), which were expected to contribute to decrease of the defects by the passivation effects. Here, effects of neodymium trifluoride (NdF3) or ytterbium trifluoride (YbF3) addition to CH3NH3PbI3 perovskite solar cells inserted with DPPS were investigated. Introduction of NdF3 or YbF3 increased the lattice constants and promoted crystal growth of the perovskites, and surface treatment by DPPS suppressed the PbI2 formation as surface passivation. Combined additions of NdF3 or YbF3 and DPPS contributed to the improvement of both the conversion efficiencies of the present perovskite devices and the stabilities of the photovoltaic properties by inhibiting the decomposition.

Neodymium(III) ortho-oxidotungstate(VI) was synthesized as a side-product in an unsuccessful synthesis attempt at fluoride derivatives of neodymium tungstate in fused silica ampoules, using neodymium(III) oxide, neodymium(III) fluoride and tungsten trioxide. Violet, platelet-shaped single crystals of the title compound emerged of the bulk, which crystallize in the defect scheelite type with a trigonal dodecahedral coordination of oxide anions around the Nd3+ cations and the hexavalent tungsten cations situated in the centers of oxide tetrahedra.

Experimental studies and group-theoretical analysis of low-temperature optical absorption spectra of neodymium ferroborate crystal NdF e 3 (B O 3) 4 were carried out. It was shown that the sign of exchange interaction with the iron subsystem in an excited state of N d 3 + can be different from that in the ground state. [ABSTRACT FROM AUTHOR]