Search Results (717)

To address the issues of high wastewater treatment costs and the lack of recycling associated with conventional precipitants such as oxalic acid and ammonium bicarbonate in rare earth precipitation processes, this study proposes a novel gradient alkali conversion–carbonation method based on a green process coupling “rare earth chloride alkali conversion-carbonation with sodium chloride electrolysis.” The primary scientific objective is to elucidate the crystallization mechanism and to achieve controlled preparation of high-quality lanthanum carbonate. By gradient-controlling the addition sequence and rate of alkali liquor and CO₂, lanthanum carbonate tetrahydrate was successfully synthesized. Characterization by XRD, SEM, ICP, and laser particle size analysis indicates that the product prepared by the gradient alkali conversion–carbonation method exhibits a single phase with high crystallinity, as evidenced by sharp and clear XRD diffraction peaks. Furthermore, the median particle size of the product obtained via this method is relatively large, reaching approximately 10 μm, while the particle size distribution Span value remains around 1.0. Mechanistic studies suggest that this method effectively regulates the crystallization process by precisely controlling the introduction and slow dissolution of the La(OH)₃ precursor, thereby reducing the supersaturation of the system during carbonation and facilitating the dissolution–reprecipitation of La³⁺. This work provides a theoretical basis for the preparation of high-quality rare earth carbonates and a process reference for the green recycling route. Full article

Lanthanum silicate oxyapatite (LSO) is a promising oxide ion conductor for low-temperature-operating electrochemical devices owing to its high ionic conductivity along the c-axis. However, the fabrication of thin films with controlled crystallographic orientation remains challenging. In this study, polymer-assisted deposition (PAD), a solution-based technique offering precise microstructural and compositional control, was employed to fabricate c-axis-oriented LSO thin films. The fabrication of undoped LSO and the effects of Al and Mg incorporation on its microstructure, orientation, and ionic conductivity were systematically investigated. Undoped LSO thin films crystallised with a preferential c-axis orientation in the annealing temperature range of 800 and 1100 °C, and scanning transmission electron microscopy observations revealed a highly crystalline, void-free microstructure. Upon annealing at 1200 °C, the undoped LSO exhibited columnar grains with anisotropic in-plane grain growth, whereas Al- or Mg-doped LSO suppressed anisotropic in-plane grain growth and retained an out-of-plane c-axis orientation. The undoped LSO showed higher in-plane ionic conductivity than the doped thin films, consistent with their distinct crystallographic orientations. These results demonstrate that PAD provides a viable pathway for tailoring the microstructure and the composition of LSO thin films, thereby facilitating their applications in solid oxide electrochemical devices. Full article

Ammonia decomposition represents a promising route for carbon-free hydrogen production, provided that efficient and cost-effective catalysts are developed. In this study, lanthanum-based mixed oxide catalysts (LaNi, LaCo, and LaCe) were synthesized via a controlled co-precipitation method and systematically evaluated for catalytic ammonia decomposition under atmospheric pressure in the temperature range of 350–500 °C. Comprehensive characterization combining N₂ physisorption, XRD, SEM–EDX, TGA–DTG, XPS, and FTIR-pyridine adsorption revealed pronounced structure–property relationships. LaNi exhibited the highest surface area (31.11 m²·g⁻¹), well-developed mesoporosity, and a balanced Lewis/Brønsted acidity (C_L/C_B ≈ 0.82), leading to superior catalytic performance with NH₃ conversion reaching ~48% at 500 °C (GHSV = 50 h⁻¹). LaCo showed intermediate activity (~30% conversion), while LaCe displayed limited performance (<13%), most likely due to its dense morphology and low surface accessibility. Increasing gas hourly space velocity resulted in decreased ammonia conversion for all catalysts, highlighting the critical role of residence time. These findings demonstrate that the catalytic efficiency of lanthanum-based systems is governed by the synergistic interplay between surface area, mesoporous architecture, and acidity distribution, with LaNi emerging as the most promising catalyst among the investigated materials. Full article

Magnesium–air battery anodes suffer from self-corrosion, chunk effect, and poor removal of discharge products, resulting in low anode efficiency. Although various modification strategies for Mg anodes have been reported, the effects of Ge content on the microstructure and performance of AZ61 Mg anodes at a fixed La content remain unclear. In this study, AZ61-1La-xGe alloys (x = 0, 0.25, 0.7, and 0.9 wt.%) were prepared, and their microstructure, corrosion behavior, and discharge performance after solution treatment were systematically investigated. Among them, AZ61-1La-0.7Ge exhibited the best overall performance, mainly due to the appropriate addition of Ge, which promoted a uniform distribution of secondary phases and grain refinement, thereby suppressing self-corrosion and chunk effect, improving discharge uniformity, and enhancing anode utilization by facilitating the formation of a loose discharge product layer. This study provides a basis for optimizing the Ge content in La-modified AZ61 Mg alloy anodes. Full article

Functional materials based on LaCoSi and LaCuSi intermetallic compounds (IMC) were fabricated and tested in the electrocatalytic process of reducing nitrates to ammonia (NO₃RR). The method of arc melting in an argon atmosphere was used to synthesize the alloys. The synthesis process is described and analyzed in detail, and the difficulties and advantages are shown. It has been established that when using an LaCuSi-based IMC–alloy as an electrocatalyst, the reduction of nitrates is the predominant reaction. On the contrary, for the LaCoSi (IMC)–alloy electrocatalyst, NO₃RR and the hydrogen evolution reaction (HER) occur simultaneously. Full article

The properties of a Ca₉La(VO₄)₇ single crystal were studied using dielectric spectroscopy and second-harmonic generation. The crystal structure of Ca₉La(VO₄)₇ grown using the Czochralski technique was refined using single-crystal data. The distribution of Ca²⁺ and La³⁺ cations over structural positions was determined. The crystal structure refinement results were compared with those obtained previously from powder X-ray diffraction data. It was shown that the refinement carried out using two different data sets leads to approximately the same results for the distances in the polyhedra, but their distortion is significantly less in the case of using single-crystal data for calculation. Dielectric properties and conductivity measurements were performed on polished single-crystal wafers cut parallel and perpendicular to the c axis. Second-harmonic generation and dielectric temperature measurements revealed the presence of a reversible ferroelectric first-order phase transition at about 1224 K from the ferroelectric β-phase (space group R3c) to the paraelectric β′-phase. The ferroelectric–paraelectric phase transition is accompanied by a complex structural rearrangement, including a 60° rotation of the V1O₄ tetrahedron, as well as slight displacements of the Ca²⁺ and La³⁺ cations. It has been shown that the conductivity differs only slightly along the polar axis and perpendicular to it. Above the phase transition temperature, the activation energy of the conductivity is the same for all directions, E_a~1.2 eV. The influence of composition on the phase transition temperature and the formation of ferroelectric and nonlinear optical properties is discussed. Full article

Interest in non-centrosymmetric crystalline materials exhibiting second harmonic generation (SHG) has increased due to their potential applications in optical sensing and biosensing. Saccharide-based metal complexes are particularly attractive systems, as chiral sugars can promote non-centrosymmetric crystal packing. In this work, a new lanthanum–β-d-fructose compound, [La(C₆H₁₂O₆)(H₂O)₅]Cl₃ (LaFRUCl), was synthesized using a simple and low-cost method and characterized by single-crystal X-ray diffraction. The compound crystallizes in the orthorhombic space group P2₁2₁2₁ and consists of infinite (La³⁺–fructose)_n chains extending along the [001] direction, forming a one-dimensional Metal–Organic Framework. The nonlinear optical response was evaluated using the Kurtz–Perry powder technique with a Nd:YAG laser (1064 nm) and compared to a sucrose reference. The measured SHG efficiency is comparable to that of previously reported alkaline earth metal–sugar analogs. While the compound’s SHG emission is significant, evaluation of its structural stability under aqueous or physiological conditions is be required before considering biological applications. Full article

Phytic acid (myo-inositol hexakisphosphate) and its salts, including iron, aluminum, sodium, and lanthanum phytate, are perhaps the most recent discovery in the field of bio-sourced flame retardants. Phytic acid can be extracted from sustainable resources, such as beans, cereals, and oilseeds. Its high phosphorus content (28 wt.% based on molecular weight) organized into six phosphate groups justifies the growing interest this biomolecule has attracted over the last decade in various sectors (as a corrosion inhibitor, antioxidant, and anticancer additive, among others). In addition, when exposed to a flame or an irradiative heat flux, phytic acid is a highly efficient dehydrating and char-forming agent. It also contributes to excellent flame-retardant properties when combined with other carbon sources, such as chitosan, or nitrogen-containing additives, including melamine, urea, and polyethyleneimine. This paper reviews the most recent advances in using phytic acid and its derivatives to design effective flame-retardant systems for textiles, bulk polymers, and foams. It also provides perspectives on possible future developments and implementations. Full article

Biofilm-associated infections remain a major barrier to wound healing, implant integration, and chronic infection management. Rare-earth oxides (REOs) have emerged as promising antibiofilm materials, though their mechanisms, limitations, and translational potential are still being defined. Cerium oxide (CeO₂) serves as the benchmark due to its redox adaptability, oxygen-vacancy-driven catalytic activity, and host compatibility. In contrast, non-ceria REOs show antibiofilm effects under more restricted conditions, often requiring surface functionalization, composite architectures, or hybrid organic–inorganic interfaces—such as polyphenol coatings or hydroxyapatite-based composites—to achieve comparable activity. Across systems, biofilm control arises not from bactericidal potency but from matrix-level mechanisms including extracellular polymeric substance (EPS) destabilization, extracellular DNA (eDNA) sequestration, redox modulation, and quorum-sensing interference. Preclinical and near-clinical evidence, particularly in chronic wound models, supports the translational relevance of these mechanisms, though the evidence base remains preliminary. This review synthesizes mechanistic data across cerium-, samarium-, lanthanum-, and strontium-based systems to establish a unified framework for REO-mediated biofilm disruption. REOs are positioned as biofilm-modulating platforms that complement antibiotics, enhance healing, and improve outcomes. Design rules emphasize controlled redox activity, targeted coordination chemistry, functional surface engineering, and host-compatible performance, alongside regulatory and manufacturing guidance for future development. Full article

To address the dual challenges of aqueous phosphate pollution and the resource utilization of petrochemical solid wastes, this study proposes a novel closed-loop “waste-to-waste” strategy. This approach innovatively integrates multiple solid wastes (including oily sludge and petroleum hydrocarbon-contaminated soil) into a porous ceramic matrix and utilizes lanthanum recovered from spent catalysts for surface modification, successfully fabricating an optimized adsorbent—lanthanum-modified ceramsite (BC@La). Under the conditions of pH 6, an adsorbent dosage of 1 g/L, and a temperature of 318 K, BC@La achieved a maximum phosphate adsorption capacity of 2.56 mg/g, corresponding to 128.0 mg of phosphorus per gram of La. Kinetic and isotherm analyses revealed that the adsorption process followed the pseudo-second-order model and fitted well with the Langmuir isotherm, consistent with monolayer chemisorption. Thermodynamic studies further indicated that the adsorption was spontaneous and endothermic. The primary adsorption mechanism was attributed to the precipitation of lanthanum phosphate (LaPO₄). This study not only demonstrates a high-performance adsorbent but also provides a sustainable strategy for the synergistic utilization of industrial solid wastes. Full article

Nitrogen oxides (NO_x), carbon monoxide (CO), sulfur dioxide (SO₂), and volatile organic compounds (VOCs) in industrial waste gases pose significant threats to environmental quality and human health. Catalytic purification is recognized as a leading abatement technology, crucial for meeting increasingly stringent emission regulations. Rare-earth (RE) catalytic materials, particularly those based on cerium (Ce), lanthanum (La), praseodymium (Pr), and neodymium (Nd) oxides, have attracted intense research due to their unique electronic configurations, high oxygen storage capacity (OSC), facile reversible redox reactions Ce⁴⁺, Ce³⁺, and exceptional thermal stability. This paper provides a comprehensive and methodical overview of RE catalysts used in industrial waste-gas purification. Initially, the physicochemical characteristics of RE elements and their multifaceted roles as active phases, supports, and promoters are explained. Subsequently, the latest developments in RE-based catalysts for NO_x abatement, CO oxidation, VOC degradation, and the removal of sulfur-bearing gas are critically reviewed. The discussion emphasizes structure–activity relationships, reaction mechanisms, and the synergistic interactions between RE elements and transition metals. Comparative analyses are presented through tables focusing on catalyst composition, reaction conditions, performance parameters, and stability. Special attention is given to the enhanced resistance to water vapor and sulfur poisoning afforded by RE materials. Finally, current challenges and future research prospects, including cost reduction, scalability, and long-term durability, are suggested. This review aims to provide practical guidance for the rational design and industrial translation of next-generation RE catalytic materials for air pollution control. Full article

In agriculture, the use of Porous Coordination Polymers (PCPs), also known as Metal–Organic Frameworks (MOFs), has emerged as a promising area of research for biological applications, particularly as long-lasting delivery systems for biostimulant chemical compounds. The objective of this study was to evaluate the effect of different concentrations of the hybrid compound La(NO₃)₃@Zn-MOF and La(NO₃)₃·6H₂O on the in vitro growth of sugarcane cv. Mex 69–290. To assess the effect on sugarcane (Saccharum spp. L.), plantlets were grown in flasks containing Murashige and Skoog (MS) liquid medium without growth regulators. Each treatment consisted of three independent culture flasks, each containing three sugarcane plantlets, and different concentrations (0, 2.5, 5, 10, and 20 mg L⁻¹) of La(NO₃)₃@Zn-MOF and La(NO₃)₃·6H₂O were added separately. After 30 days of culture, various growth variables were evaluated, including explant length, number of leaves, number and length of shoots, fresh matter, dry matter, and chlorophyll content (a, b, and total). The 5 mg L⁻¹ concentration of La(NO₃)₃@Zn-MOF increased the number of shoots and leaves in the sugarcane plantlets, and significant increases in fresh and dry matter were observed, while no statistically significant differences were detected in explant length, shoot length, or chlorophyll a, b, and total chlorophyll. However, inhibitory effects were observed at concentrations of 10 and 20 mg L⁻¹ of La(NO₃)₃@Zn-MOF and La(NO₃)₃·6H₂O, respectively. In conclusion, the hybrid compound La(NO₃)₃@Zn-MOF exhibited biostimulatory effects on sugarcane growth and physiology under in vitro conditions, whereas high concentrations of the lanthanum(III) salt caused toxicity symptoms in the sugarcane plantlets. Full article

The paper focuses on materials characterization and in vivo biocompatibility tests of Ti–6Al–7Nb–0.3REE wt.% alloys (REEs—Y, Ce, La) for use as a promising material to produce personalized medical implants and shed light on possible toxicity effects of REE alloy microdoping. All alloys were produced by the electric arc melting method and characterized by scanning electron microscopy (SEM), optical microscopy (OM), energy-dispersive X-ray spectroscopy analysis (EDX), X-ray diffraction (XRD), true density analysis, micro- and nanoindentation methods, and reducing/oxidation melting techniques. True density of alloys increased in the following order: Ti−6Al−7Nb−0.3Y (4.4563 ± 0.1075 g/cm³) < Ti−6Al−7Nb−0.3Ce (4.7255 ± 0.2853 g/cm³) < Ti−6Al−7Nb−0.3La (4.8019 ± 0.0111 g/cm³). XRD analysis indicated that Ti–6Al–7Nb–0.3Y alloy consisted of single α–Ti phase in comparison with Ti–6Al–7Nb–0.3La (α–Ti to β–Ti = 82 to 18) and Ti–6Al–7Nb–0.3Ce (α–Ti to β–Ti = 90.5 to 9.5). The single-phase Ti–6Al–7Nb–0.3Y alloy had the finest α–Ti phase crystallites (22.32 nm); the larger α–Ti crystallites in the dual-phase Ti–6Al–7Nb–0.3Ce and Ti–6Al–7Nb–0.3La (30.77 nm and 29.83 nm, respectively) suggested the presence of the β–Ti phase (23.34 nm and 25.61 nm, respectively). REE microdoping of alloys changed the lattice volume (∆V): α–Ti phase—0.269% for Ti–6Al–7Nb–0.3Y, 1.799% for Ti–6Al–7Nb–0.3Ce, 0.595% for Ti–6Al–7Nb–0.3La; and β–Ti phase—0.334% for Ti–6Al–7Nb–0.3Ce, 0.670% for Ti–6Al–7Nb–0.3La. Nanohardness (H) and elastic modulus (E) increased in the following order: Ti−6Al−7Nb−0.3La (4.01 GPa and 135 GPa, respectively) < Ti−6Al−7Nb−0.3Y (4.39 GPa and 137 GPa, respectively) < Ti−6Al−7Nb−0.3Ce (4.67 GPa and 146 GPa, respectively). In vivo tests were conducted using 46 sexually mature male Wistar rats by means of skin implantation of samples with d = 11 mm and h = 1 mm. Our research shows that Ti–6Al–7Nb–0.3La alloy (Group 2) and Ti–6Al–7Nb–0.3Ce alloy (Group 3) induced sustained hepatotoxic and nephrotoxic effects. Ti–6Al–7Nb–0.3Y alloy induced a slight local inflammatory response; however, serum biochemical analysis suggested this effect was compensated. Full article

Water with a high fluoride content poses a serious threat to both public health and the natural environment. To enhance fluoride ion removal efficiency, a modified activated carbon adsorbent (HPAC-La) was synthesized by impregnating soybean protein in a lanthanum nitrate solution, followed by freezing–drying and carbonization. The results confirmed that lanthanum nitrate modification significantly improved the adsorption performance. Under optimised experimental conditions (pH = 2.0, [F⁻] = 300 mg·L⁻¹, 12 h, 298 K), HPAC-La exhibited a maximum adsorption capacity for fluoride ions of 126.7 mg·L⁻¹, significantly higher than that of unmodified HPAC (86.1 mg·L⁻¹). The adsorption process followed the pseudo-second-order kinetic model and the Langmuir isotherm model, indicating monolayer chemisorption. The mechanism involves ion exchange via surface hydroxyl groups and fluoride coordination with La sites. This study proposes a method for developing highly efficient adsorbents for the treatment of fluoride-contaminated wastewater. Full article