Precious Metals Research Articles

Investigation into Recycling of Iron Oxide Scale on H13 Steel by Low‐Temperature Carbothermal Reduction Method

The current method for recovering iron oxide scale in the steel industry is not economically optimal, especially for high‐alloy scales found in alloyed steel. This study focuses on iron oxide scale containing valuable metals like chromium (Cr), molybdenum (Mo), and vanadium (V). The required carbon addition is calculated based on the iron and chromium oxides in the scale. The effects of varying carbon additions and reduction temperatures on reduction efficiency are thoroughly examined. Kinetic studies show that as temperature and carbon increase, the rate‐limiting step shifts from interfacial diffusion to interfacial reaction. Reduction experiments assess carbon utilization, metallization rate, deoxidation rate, and removal of harmful elements. Results show that high temperatures hinder sulfur (S) and phosphorus (P) removal, and excess carbon reduces carbon utilization efficiency. Optimal conditions are a carbon ratio of 0.2174 and a temperature of 1150 °C. The carbothermic reduction product requires further refinement through conventional ladle slag systems to meet the quality standards for metallic materials. Over 65% of alloying elements are recovered, though phosphorus content remains slightly higher than in finished alloy steel. The materials from this study are suitable as high‐quality intermediates for alloy steel production.

Light-Promoted Extraction of Precious Metals Using a Porphyrin-Integrated One-Dimensional Covalent Organic Framework.

Precious metals are valuable materials for the chemical industry, but they are scarce and pose a risk of supply disruption. Recycling precious metals from waste is a promising strategy, here we tactfully utilize light irradiation as an environmental-friendly and energy-saving adjunctive strategy to promote the reduction of precious metal ions, thereby improving the adsorption capacity and kinetics. A newly light-sensitive covalent organic framework (PP-COF) was synthesized to illustrate the effectiveness and feasibility of this light auxiliary strategy. The equilibrium adsorption capacities of PP-COF with light irradiation towards gold, platinum, and silver ions are 4729, 573, and 519 mg g-1, which are 3.3, 1.9, and 1.2 times the adsorption capacities under dark condition. Significantly, a filtration column with PP-COF can recover more than 99.8 % of the gold ions in the simulated e-waste leachates with light irradiation, and 1 gram of PP-COF can recover gold from up to 0.15 tonne of e-waste leachates. Interestingly, the captured precious metals by PP-COF with light irradiation mainly exist in the micron-sized particles, which can be easily separated by extraction. We believe this work can contribute to precious metal recovery and circular economy for recycling resources.

Light‐Promoted Extraction of Precious Metals Using a Porphyrin‐Integrated One‐Dimensional Covalent Organic Framework

AbstractPrecious metals are valuable materials for the chemical industry, but they are scarce and pose a risk of supply disruption. Recycling precious metals from waste is a promising strategy, here we tactfully utilize light irradiation as an environmental‐friendly and energy‐saving adjunctive strategy to promote the reduction of precious metal ions, thereby improving the adsorption capacity and kinetics. A newly light‐sensitive covalent organic framework (PP‐COF) was synthesized to illustrate the effectiveness and feasibility of this light auxiliary strategy. The equilibrium adsorption capacities of PP‐COF with light irradiation towards gold, platinum, and silver ions are 4729, 573, and 519 mg g−1, which are 3.3, 1.9, and 1.2 times the adsorption capacities under dark condition. Significantly, a filtration column with PP‐COF can recover more than 99.8 % of the gold ions in the simulated e‐waste leachates with light irradiation, and 1 gram of PP‐COF can recover gold from up to 0.15 tonne of e‐waste leachates. Interestingly, the captured precious metals by PP‐COF with light irradiation mainly exist in the micron‐sized particles, which can be easily separated by extraction. We believe this work can contribute to precious metal recovery and circular economy for recycling resources.

Programmable C−N Bond Formation through Radical‐Mediated Chemistry in Plasma‐Microdroplet Fusion

AbstractNon‐thermal plasma discharge produced in the wake of charged microdroplets is found to facilitate catalyst‐free radical mediated hydrazine cross‐coupling reactions without the use of external light source, heat, precious metal complex, or trapping agents. A plasma‐microdroplet fusion platform is utilized for introduction of hydrazine reagent that undergoes homolytic cleavage forming radical intermediate species. The non‐thermal plasma discharge that causes the cleavage originates from a chemically etched silica capillary. The coupling of the radical intermediates gives various products. Plasma‐microdroplet fusion occurs online in a programmable reaction platform allowing direct process optimization and product validation via mass spectrometry. The platform is applied herein with a variety of hydrazine substrates, enabling i) self‐coupling to form secondary amines with identical N‐substitutions, ii) cross‐coupling to afford secondary amine with different N‐substituents, iii) cross‐coupling followed by in situ dehydrogenation to give the corresponding aryl‐aldimines with two unique N‐substitutions, and iv) cascade heterocyclic carbazole derivatives formation. These unique reactions were made possible in the charged microdroplet environment through our ability to program conditions such as reagent concentration (i. e., flow rate), microdroplet reactivity (i. e., presence or absence of plasma), and reaction timescale (i. e., operational mode of the source). The selected program is implemented in a co‐axial spray format, which is found to be advantageous over the conventional one‐pot single emitter electrospray‐based microdroplet reactions.

Enhanced Platinum-Based Thin-Film Catalysts for Electro-Oxidation of Methanol

Surface morphology is one of the critical factors affecting the performance of electrocatalysts. Thus, with careful manipulation of the surface structures at the atomic level, the effectiveness of the catalyst can be significantly improved. Heat treatment is an effective method for inducing surface atom rearrangement, hence modifying the catalyst’s characteristics. This study investigated the substrate’s influence and the effect of thermal annealing on the morphology and surface reconstruction of platinum (Pt) thin-film catalysts. Our findings indicate that heat treatment in a reductive atmosphere (95% Ar + 5% H2) at 300 °C can significantly impact the degree of rearrangement of surface atoms. This process induces long-range ordering, resulting in domains with a high proportion of (111) and (100) sites without an epitaxial template. Considering that the reactivity of low-index platinum single crystals for the methanol oxidation reaction follows the following sequence Pt(111) < Pt(110) < Pt(100), increasing the proportion of (100) planes leads to a notable enhancement (up to three times) in performance, compared to untreated catalysts. Furthermore, considering the amount of precious metal consumed, a mass-specific current density obtained on annealed Pt@Ni is larger by one order of magnitude and ~2 times that obtained on Pt@Cr and Pt@GCox catalysts, respectively. Our results demonstrate that an easy-to-implement way of controlling atomic orientations improves catalyst performance. With this contribution, we propose a method for designing improved electrocatalysts, as catalytic reactions occur only at the surface.

Synergistic Catalytic Sites in High-Entropy Metal Hydroxide Organic Framework for Oxygen Evolution Reaction.

The integration of multiple elements in a high-entropy state is crucial in the design of high-performance, durable electrocatalysts. High-entropy metal hydroxide organic frameworks (HE-MHOFs) are synthesized under mild solvothermal conditions. This novel crystalline metal-organic framework (MOF) features a random, homogeneous distribution of cations within high-entropy hydroxide layers. HE-MHOF exhibits excellent electrocatalytic performance for the oxygen evolution reaction (OER), reaching a current density of 100mA cm-2 at ≈1.64 VRHE, and demonstrates remarkable durability, maintaining a current density of 10mA cm-2 for over 100 h. Notably, HE-MHOF outperforms precious metal-based electrocatalysts despite containing only ≈60% OER active metals. Ab initio calculations and operando X-ray absorption spectroscopy (XAS) demonstrate that the high-entropy catalyst contains active sites that facilitate a multifaceted OER mechanism. This study highlights the benefits of high-entropy MOFs in developing noble metal-free electrocatalysts, reducing reliance on precious metals, lowering metal loading (especially for Ni, Co, and Mn), and ultimately reducing costs for sustainable water electrolysis technologies.

Collembola growth in heavy metal-contaminated soils.

Collembola play a key role in soil ecosystems by decomposing organic matter. Most of them inhabit the upper layers of the soil and are susceptible to contamination present in the pore water. These arthropods serve as model organisms in ecotoxicology for short and long-term exposure. This study aimed to assess the toxicity of three heavy metals (lead [Pb], cadmium [Cd], and copper [Cu]) using the springtail species Folsomia candida as the test organism, with mortality and growth inhibition as the measure of toxicity. We hypothesised that increasing metal concentrations in the soil would correspond to a growth reduction of Collembola. Each heavy metal was tested at a minimum of eight increasing concentrations in six replications. Twenty 10-12-day-old individuals were introduced into each test container filled with contaminated or control soil and incubated for 14 days. The test endpoints included growth inhibition determined by comparing F. candida growth rates in contaminated soil with those in control soil, as well as mortality rates. The EC50 values (mg/kg) for heavy metals were as follows: Cd = 66.89, Cu = 791.01, Pb = 10075.48. Our findings suggest that growth inhibition is a reliable indicator of Collembola toxicity to heavy metals.

Exploring Structural Anisotropy in Amorphous Tb-Co via Changes in Medium-Range Ordering.

Amorphous thin films grown by magnetron co-sputtering exhibit changes in atomic structure with varying growth and annealing temperatures. Structural variations influence the bulk properties of the films. Scanning nanodiffraction performed in a transmission electron microscope (TEM) is applied to amorphous Tb17Co83 (a-Tb-Co) films deposited over a range of temperatures to measure relative changes in medium-range ordering (MRO). These measurements reveal an increase in MRO with higher growth temperatures and a decrease in MRO with higher annealing temperatures. The trend in MRO indicates a relationship between the growth conditions and local atomic ordering. By tilting select films, the TEM measures variations in the local atomic structure as a function of orientation within the films. The findings support claims that preferential ordering along the growth direction results from temperature-mediated adatom configurations during deposition, and that oriented MRO correlates with increased structural anisotropy, explaining the strong growth-induced perpendicular magnetic anisotropy found in rare earth-transition metal films. Beyond magnetic films, we propose the tilted FEM workflow as a method of extracting anisotropic structural information in a variety of amorphous materials with directionally dependent bulk properties, such as films with inherent bonding asymmetry grown by physical vapor deposition.

Iron-Based Layered Perovskite Oxyfluoride Electrocatalyst for Oxygen Evolution: Insights from Crystal Facets with Heteroanionic Coordination.

Mixed-anion compounds have recently attracted attention as solid-state materials that exhibit properties unattainable with those of their single-anion counterparts. However, the use of mixed-anion compounds to control the morphology and engineer the crystal facets of electrocatalysts has been limited because their synthesis method is still immature. This study explored the electrocatalytic properties of a Pb-Fe oxyfluoride, Pb3Fe2O5F2, with a layered perovskite structure for oxygen evolution reaction (OER) and compared its properties in detail with those of a bulk-type cubic three-dimensional (3D) perovskite, PbFeO2F. A Pb3Fe2O5F2 electrode prepared with carbon nanotubes and a graphite sheet as a conductive support and a substrate, respectively, demonstrated better OER performance than a PbFeO2F electrode. The role of specific crystal facets of Pb3Fe2O5F2 in enhancing the OER activity was elucidated through electrochemical analysis. Density functional theory calculations indicated that the Pb3Fe2O5F2 (060) facet with Fe sites exhibited a lower theoretical overpotential for the OER, which was attributed to a moderately strong interaction between the active sites and the reaction intermediates; this interaction was reinforced by the strong electron-withdrawing behavior of fluoride ions. This finding offers new insights for developing efficient electrocatalysts based on oxyfluorides, leveraging the high electronegativity of fluorine to optimize the electronic states at active sites for the OER, without relying on precious metals.

A multi-wavelength overview of the giant spiral UGC 2885

UGC 2885 ($z = 0.01935$) is one of the largest and most massive galaxies in the local Universe, yet it has an undisturbed spiral structure, which is unexpected for such an object and is not predicted by cosmological simulations. Understanding the detailed properties of extreme systems such as UGC 2885 can provide insight into the limits of scaling relations and the physical processes driving galaxy evolution. Our goal is to understand whether UGC 2885 has followed a similar evolutionary path as other high-mass galaxies by examining its place in the fundamental metallicity relation and on the star-forming main sequence. We present new observations of UGC 2885 with the Canada-France-Hawaii Telescope and the Institut de radioastronomie millimétrique 30 m telescope. We used these novel data to calculate metallicity and molecular hydrogen mass values, respectively. We estimated the stellar mass (M$_ star $) and star formation rate (SFR) based on mid-infrared observations with the Wide-field Infrared Survey Explorer. We find global metallicities $Z = 9.28$, 9.08, and 8.74 at the 25 kpc ellipsoid from the N2O2, R23, and O3N2 indices, respectively. This puts UGC 2885 at the high end of the galaxy metallicity distribution. We find a molecular hydrogen mass of M$_ $ M$_ odot $, a SFR of $1.63 odot $ yr$^ $, and a stellar mass of $4.83 $ M$_ odot $, which gives a star formation efficiency ($ SFR $) of $8.67 $ yr$^ $. This indicates that UGC 2885 has an extremely high molecular gas content compared to known samples of star-forming galaxies ($ times more) and a relatively low SFR for its current gas content. We conclude that UGC 2885 has gone through cycles of star formation periods, which increased its stellar mass and metallicity to its current state. The mechanisms that are fuelling the current molecular gas reservoir and keeping the galaxy from producing stars remain uncertain. We discuss the possibility that a molecular bar is quenching star-forming activity.

High‐Throughput Screening of Dual‐Atom Catalysts for Methane Combustion: A Combined Density Functional Theory and Machine‐Learning Study

AbstractCeria‐supported precious metal catalysts have undergone extensive investigation for the catalytic methane combustion. However, it remains a significant challenge to achieve both highly synergistic oxidation activity and efficient atom utilization remains a challenge for commonly used supported nanoparticles and single‐atom catalysts. Dual‐atom catalysts (DACs) emerges as a frontier of advanced catalysts, presenting unique catalytic properties that benefit from the synergy of neighboring metal sites. In this study, 361 ceria‐supported DACs (M1M2/CeO2) encompassing combinations of 19 transition metals are systematically explored. Using high‐throughput density functional theory calculations, the structures, stability as well as activity of M1M2/CeO2 are assessed. Notably, Au1Ga1/CeO2 is identified as a promising DAC exhibiting high activity for methane total oxidation, substantiated by comprehensive DFT‐calculated reaction pathways. Furthermore, employing six machine‐learning algorithms, the structure‐properties relationship is explored within ceria‐based DACs and highlight the importance of oxidation states and atomic radii of doped metals as the descriptors. The trained model by computational dataset exhibits high accuracy and predict a more active Mn1Au1/CeO2 than those screened using only DFT datasets. The high‐throughput strategy demonstrated in this work not only provides insights into the rational design of methane oxidation catalysts, but also paves the way for exploring DACs for diverse applications.

Recent Advances in Indium Recovery

Though indium has been removed from the fifth list (2023) of critical raw materials for the European Union list of critical metals, its recovery is still of paramount importance due to its wide use in a series of high-tech industries. As its recovery is closely associated with zinc mining, the recycling of In-bearing wastes is also of interest, for both profitable and environmental reasons. With unit operations (in hydrometallurgy and pyrometallurgy or extractive metallurgy) playing a key role in the recycling of indium, the present work reviewed the most recent innovations (2024) regarding the use of these operations in the recovery from this valuable metal from different solid or liquid wastes.

Fe‐Catalyzed α‐C(sp3)−H Amination of N‐Heterocycles

AbstractNitrogen‐heterocycles are privileged structures in both marketed drugs and natural products. On the other hand, C−H amination reactions furnish unconventional and straightforward approaches for the construction of C−N bonds. Yet, most of the known methods rely on precious metal catalysts. Herein we report a site‐selective intermolecular C(sp3)−H amination of N‐heterocycles, catalyzed by inexpensive FeCl2, which allows the functionalization of a wide range of pharmaceutically relevant cyclic amines. The C−H amination occurs site‐selectively in α‐position to the nitrogen atom, even when weaker C−H bonds are present, and furnishes Troc‐protected aminals or amidines. The method employs the N‐heterocycle as limiting reagent and is applicable to the late‐stage functionalization of complex molecules. Its synthetic potential was further illustrated through the derivatization of α‐aminated products and the application to a concise total synthesis of the reported structure for senobtusin. Mechanistic studies allowed to propose a plausible reaction mechanism involving a turnover‐limiting Fe‐nitrene generation followed by fast H atom transfer and radical rebound.

UNDER THE LOAN: AN ANALYSIS OF ARMENIAN BANKING SECTOR AND CREDIT TRENDS

This study examines recent trends in Armenia's banking sector and export patterns, revealing underlying economic vulnerabilities despite apparent growth. Using data from the Central Bank of Armenia and official trade statistics, this paper analyzes shifts in lending patterns across various economic sectors and changes in export composition. Our findings indicate a concerning decline in industrial sector lending, coupled with a significant increase in mortgage and consumer loans. Additionally, we observe a heavy reliance on precious metal re-exports for economic growth, raising questions about the sustainability of Armenia's current economic trajectory. This research contributes to the understanding of potential risks in Armenia's financial system and highlights the need for diversification in its export base.

Leaching Kinetics of Valuable Metals from Calcined Material of Spent Lithium-Ion Batteries

Leaching Kinetics of Valuable Metals from Calcined Material of Spent Lithium-Ion Batteries

Solvent Extraction of Gallium and Germanium Using a Novel Hydroxamic Acid Extractant

The rare metals gallium and germanium are key strategic metals that are widely used in emerging industries. In this work, a novel hydroxamic acid extractant, BGYW, with low toxicity, was used for the selective solvent extraction of Ga ions and Ge ions from Zn, As, Cu, and Al ions in the solution from zinc smelting. The gallium and germanium ions were extracted efficiently under optimized conditions. Gallium ions were preferentially stripped using sulfuric acid, and germanium ions were stripped using an ammonium fluoride solution. Compared with the commercial extractant YW100, the dissolution loss of BGYW was reduced by 10 times. After 15 cycles, the germanium solvent extraction efficiency of BGYW remained at 100%, and the solvent extraction efficiency of gallium was about 98.7%, while the solvent extraction efficiency of both Ga ions and Ge ions using YW100 decreased to 20% after five cycles. This novel solvent extraction system exhibits considerable promise for application in zinc smelting processes for gallium and germanium solvent extraction.

The Thermomechanical, Functional and Biocompatibility Properties of a Au–Pt–Ge Alloy for PFM Dental Restorations

A high-noble Au–Pt–Ge porcelain-fused-to-metal (PFM) dental alloy without the known adverse metallic elements and with the addition of germanium (Ge) was produced as a more cost-effective alternative to other precious alloying metals, with investigations for determining the functionality and clinical use of this alloy. The thermomechanical, biocompatibility, durability, workability and economic characteristics of the produced dental alloy were investigated. These properties were investigated with in vitro biocompatibility testing on human gingival fibroblasts (HGFs); static immersion testing for metal ion release; DSC analysis; hardness, tensile testing, density and coefficient of thermal expansion (CTE) measurements; metallographic and SEM/EDX microstructure investigations; and finally with the production of a test PFM dental bridge. The results of the thermomechanical testing showed alloy properties suitable for dental restorations and clinical use, with somewhat lower mechanical properties, making the alloy not suitable for extensive multiunit fixed restorations. The microstructure investigations showed segregations of Ge in the homogeneous alloy matrix, which reduce the alloy’s mechanical properties. The produced PFM dental bridge showed excellent workability of the alloy in a dental laboratory setting, as well as a high standard of the final dental restoration. The ion release was negligible, well below any harmful quantities, while the cell viability examination showed significantly higher viability ratings on polished alloy samples as compared to as-cast samples. The results showed that a dental substructure in direct contact with oral tissue and fluids should be highly polished. The performed investigations showed that the produced PFM dental alloy is suitable for clinical use in producing high-quality dental restorations with high biocompatibility for patients prone to metal allergies.

Valuable metals recovery from spent ternary lithium-ion battery: A review

Valuable metals recovery from spent ternary lithium-ion battery: A review

Novel Catalyst Formulations for Enhanced Fuel Cell Efficiency

The quest for enhanced fuel cell efficiency is pivotal in advancing sustainable energy solutions. This paper investigates novel catalyst formulations aimed at improving the performance and longevity of fuel cells. Traditional catalysts, primarily based on precious metals such as platinum, present challenges related to cost and resource availability. In response, this study explores non-precious metal catalysts (NPMCs), composite materials, and nanostructured catalysts, which have shown promising results in recent research. Through rigorous experimental methods, including synthesis and characterization techniques, we evaluate the catalytic activity and efficiency of these novel formulations. The findings demonstrate significant improvements in power output and operational durability compared to conventional catalysts. Mechanistic insights into the reaction dynamics reveal how these new materials enhance performance metrics such as current density and voltage output. An economic analysis highlights the potential for scalability and cost-effectiveness of these innovative catalysts in commercial applications. This research underscores the critical role of catalyst design in optimizing fuel cell technology and sets the stage for future explorations aimed at overcoming existing limitations in the field. By leveraging advanced materials and formulations, we aim to contribute to the development of next-generation fuel cells with enhanced efficiency and practicality.

Comparative Study of the Nutritive and Elemental Composition of Smoked and Raw Clarias gariepinus from Three Selected Fish Farms in Ado Ekiti, Ekiti State, Nigeria

Clarias gariepinus is of economic importance in aquaculture due to its rapid growth, omnivorous diet, and potential as food source. It has been widely cultured and dispensed both in raw and smoked forms in various regions to meet the demand for fish protein This study assessed and compared the nutritional quality and elemental composition of smoked and raw samples of Clarias gariepinus. A total of twelve fish samples were analysed, six raw samples and six smoked samples with two fishes sampled from each farm tagged A, B and C. The Proximate and elemental analysis were done using standard procedures. The result of the study showed that moisture content measured in the raw Clarias gariepinus which ranged between (73.074 ± 1.59) % and (71.52 ± 1.83) %. was higher than that of the smoked fish ranging from (26.69±0.03) % to (32.21± 0.02) %. The protein content of smoked fish ranged (43.2±0.02) % to (46.78±0.01) while that of raw fish was between (20.52 ± 1.12) % and (22.15 ± 0.43) %. Similarly, the crude fat, ash, carbohydrate, and fibre content were higher in the smoked fish than raw catfish samples. The elemental composition of both smoked and raw catfish were within the permissible limit of World Health Organization. Arsenic was not detected in the muscle of the raw fish, while cadmium, chromium, lead and magnesium were present in values within WHO permissible limit and similar results was observed for the smoked fish samples. The result of this study presents the possibility of smoked catfish being more nutritious than the raw samples aside from the fact that it has more shelf life than raw fish. Also, both smoked and raw samples of the fish are safe as the values of heavy metal observed were all within the permissible limit of WHO.