Search Results (106)

Lead cake forms from dust as a result of the gas cleaning process during copper smelting. The objective of this study was to develop equipment and technology for a continuous hydrometallurgical method for extracting osmium from the lead cake. In this method, leaching is carried out using an aqueous solution of hydrogen peroxide and sulfuric acid. During the leaching, rhenium is converted into an acidic solution from which rhenium can be easily extracted into a marketable product. Osmium is predominantly converted into a solution, the processing of which, including the extraction of osmium into a marketable product, will be published later. A unit for leaching osmium–rhenium-containing cake with continuous loading for leaching, continuous feeding of leaching solutions, and continuous discharge of the leaching slurry was created. Using the simplex experimental design method, the dependence of osmium recovery on the consumption rates of hydrogen peroxide and sulfuric acid and the leaching duration was studied. Near-optimal leaching conditions were as follows: 68–70 mL of 30% hydrogen peroxide and 7 mL of concentrated sulfuric acid per 100 g of cake, 55 min of leaching, and a specific column throughput of 100 g of cake per 55 min. Nine experiments achieved 96.5% osmium recovery. Full article

Platinum group elements (PGE) are six rare highly siderophile metals which have similar chemical characteristics and occur together in mineral deposits: platinum (Pt), palladium (Pd), rhodium (Rh), ruthenium (Ru), iridium (Ir) and osmium (Os). In nature, they tend to exist in a metallic state or bond with sulfur and arsenic and occur as trace accessory minerals predominantly in mafic and ultramafic rocks. High industrial demand together with their scarcity in crustal rocks has been reflected in their inclusion in 2025 US Government’s List of Critical Minerals, European Union’s List of Critical Raw Materials and Mongolian List of 11 Critical Minerals. Although Mongolia is not currently a producer, it hosts four types of potentially economic PGE deposits: (1) Podiform chromitites associated with ophiolites; (2) Ni-Cu-PGE sulfide mineralization of rift-related mafic–ultramafic intrusions; (3) Alaskan–Uralian type arc related zoned mafic–ultramafic intrusions; and (4) Placers. Particularly promising are Permian Ni-Cu-PGE sulfide bearing mafic–ultramafic intrusions of the Khangai large igneous province which bear resemblance to mineralized Permian intrusions in Russia (e.g., Norilsk-Talnakh) and N.W. China (e.g., Kalatongke; Tarim basin). In addition, sub-economic ophiolite-hosted PGE mineralization can be extracted as a by-product during chromite mining. There is also the potential for PGE recovery as a by-product in existing gold placer operations in areas hosting ophiolitic massifs and Alaskan–Uralian type intrusions. Mongolia is a promising frontier for PGE exploration and mining. Full article

Osmium is an element of the Periodic Table with an atomic number Z equal to 76. In Tokamaks with divertors made of tungsten ($Z=74$), it is produced in the neutron-induced transmutation of the latter. Therefore one can expect that their sputtering may generate ionic impurities of all possible charge states in the fusion plasma. As a consequence, these could contribute to radiation losses in these controlled nuclear devices. The knowledge of radiative rates in all the spectra of osmium is thus important in this field. In this framework, a multiplatform approach has been used to determine the Os V radiative properties and estimate their accuracy. The transition probabilities have been computed for the 2677 electric dipole (E1) transitions falling in the spectral range from 400 Å to 12,000 Å. Three independent atomic structure models have been considered; one based on the fully relativistic ab initio multiconfiguration Dirac–Hartree–Fock (MCDHF) method and two based on the semi-empirical pseudo-relativistic Hartree–Fock (HFR) method. Full article

Platinum group metals (PGMs)—comprising platinum (Pt), palladium (Pd), rhodium (Rh), iridium (Ir), ruthenium (Ru), and osmium (Os)—are indispensable strategic materials for key industries, including automotive manufacturing, petrochemical engineering, and the new energy sector. Given the uneven global distribution of primary PGM reserves and the widening supply–demand gap, recovering PGMs from secondary sources—primarily metallurgical by-products and spent catalysts—has become a strategic priority. synergistic smelting, leveraging “multi-feedstock complementarity” and “multi-technology coupling,” offers an efficient approach to overcoming challenges associated with secondary resources, such as low grades, complex matrices, and refractory separation. This paper systematically reviews the technological evolution of synergistic smelting for PGMs recovery, focusing on three aspects: the characteristics and processing bottlenecks of PGMs-bearing secondary resources, the development trajectory of traditional metallurgical technologies, and innovative breakthroughs in microwave-assisted synergistic smelting. A comparative analysis between traditional and microwave-based technologies is conducted across four dimensions: resource adaptability, technical performance, environmental sustainability, and industrial maturity. Finally, the core challenges currently confronting microwave-assisted synergistic smelting and future directions for industrial demonstration are elaborated on. This study serves as a comprehensive reference for the efficient and sustainable recovery of PGMs, with significant implications for the circular economy and strategic resource security. Full article

Cancer ranks as a major cause of morbidity and mortality across the globe, notably in economically developed regions, and its incidence is predicted to rise in the coming decades. Metal-based compounds represent a particularly promising class of pharmaceuticals for the treatment of cancer. Following the success of platinum in cancer therapy, attention soon turned to other transition metals, particularly the platinum group metals such as ruthenium and palladium. Despite the high anticancer efficacy of many of its compounds, osmium remained one of the least investigated of these metals for a long time, partly due to concerns about its toxicity. However, there has been a recent resurgence in the preparation and evaluation of osmium complexes, which exhibit high structural variability and demonstrate promising anticancer activity. The present review aims to survey recent developments in this exciting field, focusing on osmium complexes of the non-arene type reported during the last decade. Full article

Rhenium is one of the rarest and most strategically important metals, indispensable in high-temperature superalloys and platinum–rhenium catalysts used across the aerospace and petrochemical industries. Owing to its limited primary reserves, recovering rhenium from secondary sources, such as spent catalysts, superalloy residues, and metallurgical dusts, has become vital to ensuring supply security. This review examines technological developments between 1998 and 2025, focusing on how operational parameters, including temperature, leaching time, reagent concentration, and solid-to-liquid ratio, govern dissolution kinetics and overall process efficiency. Comparative evaluation of hydrometallurgical, alkaline, and hybrid processes indicates that modern systems can achieve recovery rates exceeding 98% through selective oxidation, alkaline activation, or combined pyro and hydrometallurgical mechanisms. Acid–chlorine leaching facilitates rapid, low-temperature dissolution; alkaline sintering stabilises rhenium as soluble perrhenates; and hybrid smelting routes enable the concurrent separation of rhenium and osmium. Sustainable aqueous systems employing nitric and ammonium media have also demonstrated near-complete recovery at ambient temperature under closed-loop recycling conditions. Collectively, these findings highlight a technological transition from energy-intensive, acid-based pathways towards low-impact, recyclable, and digitally optimised hydrometallurgical processes. The integration of selective oxidants, phase engineering, circular reagent management, and artificial intelligence-assisted modelling is defining the next generation of rhenium recovery, combining high extraction yields with reduced environmental impact and alignment with global sustainability goals. Full article

Redox mediators are central to electrochemical biosensors, enabling electron transfer between deeply buried enzymatic cofactors and electrode surfaces when direct electron transfer is kinetically inaccessible. Among all design parameters, the reversibility of mediator redox cycling remains the most decisive yet under-examined factor governing biosensor stability, drift and long-term reproducibility. This review establishes reversibility as a unifying framework grounded in inorganic and organometallic redox chemistry, with particular emphasis on coordination environments, ligand-field effects and outer-sphere electron-transfer pathways. Recent advances (2010–2025) in ruthenium and osmium polypyridyl complexes, cobalt macrocycles, hexacyanoferrates and Prussian Blue analogues are examined alongside ferrocene derivatives and other organometallic mediators, which together define the upper limits of reversible behaviour. Organic mediator families, including quinones, phenazines, indophenols, aminophenols and viologens, are discussed as mechanistic contrasts that highlight the structural and thermodynamic constraints that limit long-term cycling in aqueous media. Mechanistic indicators of reversibility, including peak separation, current ratios and heterogeneous electron-transfer rate constants, are linked to mediator architecture, coordination chemistry and immobilisation environment. By integrating molecular electrochemistry with applied sensor engineering, this review provides a mechanistically grounded basis for selecting or designing redox mediators that sustain efficient electron transfer, minimal fouling and calibration stability across diverse sensing platforms. Full article

Choline is a central metabolite that connects membrane turnover, neurotransmission, and one-carbon metabolism, and its reliable measurement across diverse biological matrices remains a significant analytical challenge. This review brings together biological context, electrochemical mechanisms, and device engineering to define realistic performance targets for choline sensors in blood, cerebrospinal fluid, extracellular space, and milk. We examine enzymatic sensor architectures ranging from peroxide-based detection to mediated electron transfer via ferrocene derivatives, quinones, and osmium redox polymers and assess how applied potential, oxygen availability, and film structure shape electron-transfer pathways. Evidence for direct electron transfer with choline oxidase is critically evaluated, with emphasis on the essential controls needed to distinguish true flavin-based communication from peroxide-related artefacts. We also examine bienzymatic formats that allow operation at low or negative bias and discuss strategies for matrix-matched validation, selectivity, drift control, and resistance to fouling. To support reliable translation, we outline reporting standards that include matrix-specific concentration ranges, reference electrode notation, mediator characteristics, selectivity panels, and access to raw electrochemical traces. By connecting biological requirements to mechanistic pathways and practical design considerations, this review provides a coherent framework for developing choline sensors that deliver stable, reproducible performance in real samples. Full article

The osmium(II) polypyridyl complex [Os(tpy)(pydppn)]²⁺ (tpy = 2,2′:6′,2″-terpyridine; pydppn = 3-(pyrid-2′-yl)-4,5,9,16-tetraaza-dibenzo[a,c]naphthacene) was synthesized and characterized to evaluate the effect of an extended planar π-system on photophysical properties and DNA interactions. This complex represents the π-expanded analog of the previously studied [Os(tpy)(pydppz)]²⁺ system. Electrochemical studies revealed a reversible Os(II)/Os(III) oxidation at +0.99 V vs. SCE and five ligand-centered reductions, generally less negative than those of the smaller pydppz analog, consistent with enhanced electron-accepting ability. In acetonitrile, the complex exhibits UV absorption bands at 328 and 473 nm and near-infrared emission at 840 nm, assigned to a long-lived ³MLCT state (τ = 110 ns, Φ = 0.02). Upon titration with calf-thymus DNA, [Os(tpy)(pydppn)]²⁺ shows a pronounced light-switch effect, hypochromism, red-shifted MLCT bands, induced circular dichroism, and an increase in DNA melting temperature (ΔT_m = 8.9 ± 0.5 °C), consistent with intercalative binding. Viscometric titrations further support intercalation, with a binding constant K_B ≈ 1.2 × 10⁶ M⁻¹. Transient absorption spectroscopy indicates that DNA binding prolongs the excited-state lifetime and modifies vibrational relaxation pathways. These results highlight how π-system extension in Os(II) complexes modulates photophysical behavior and DNA affinity, offering insights for the rational design of NIR-emitting, DNA-targeted luminescent probes and potential phototherapeutic agents. Full article

In recent years CO₂ reforming of methane has attracted great interest as it produces high CO/H₂ ratio syngas suitable for the synthesis of higher hydrocarbons and oxygenated derivatives since it is a way for disposing and recycling two greenhouse gases with high environmental impact, CH₄ and CO₂, and because it is regarded as a potential route to store and transmit energy due to its strong endothermic effect. Along with noble metals, all the group VIII metals except for osmium have been studied for catalytic CO₂ reforming of methane. It was found that the catalytic activity of Ni, though lower than those of Ru and Rh, was higher than the catalytic activities of Pt and Pd. Although noble metals have been proven to be insensitive to coke, the high cost and restricted availability limit their use in this process. It is therefore valuable to develop stable Ni-based catalysts. In this contribution, we show how their activity and coking resistivity are greatly related to the size and dispersion of Ni particles. Well-dispersed Ni nanoparticles were achieved by multistep impregnation on a mesoporous silica support, namely SBA-15, obtained through a sol-gel method, using acetate as a nickel precursor and keeping the Ni loading between 5% and 11%. Significant catalytic activity was obtained at temperatures as low as 450 °C, a temperature well below their deactivation temperature, i.e., 700 °C. For the pre-reduced samples, a CO₂ conversion higher than 99% was obtained at approximately 680 °C. As such, their deactivation by sintering and coke formation was prevented. To the best of our knowledge, no Ni-based catalysts with complete CO₂ conversion at temperatures lower than 800 °C have been reported so far. Full article

Hydrophilic polymer–osmium complexes enhance electron transfer between enzymes and electrodes in biosensors. In this study, hydrophobic poly(4-vinylpyridine) (PVP) was quaternized with 2-bromoethanol to synthesize water-soluble PVP(Q)-C₂H₄OH polymers (MW 60,000 and 160,000). The resulting PVP(Q)-C₂H₄OH-Os(dmo-bpy)₂Cl complexes were verified by UV-Vis, FT-IR, 1H NMR, SEM-EDS, and zeta potential analyses, confirming successful quaternization and osmium coordination with good dispersion stability. Electrochemical tests (cyclic voltammetry, multi-potential step, amperometry) demonstrated that electrodes with quaternized mediators showed greatly enhanced catalytic currents for glucose (0–20 mM), with sensitivities of 6.9791 (MW 60,000) and 6.6279 μA·mM⁻¹·cm⁻² (MW 160,000), respectively, which were 6.6–10.3 times higher than those of non-quaternized polymers. Selectivity tests showed negligible interference from common species such as ascorbic acid, dopamine, uric acid, and serotonin. Continuous glucose monitoring (CGM) electrodes were fabricated by immobilizing the mediator and glucose dehydrogenase on silanized Au electrodes. SEM, scan rate, and impedance analyses confirmed stable binding. The modified electrodes showed strong linearity (R² = 0.992) and high sensitivity (2.56 μA·mM⁻¹·cm⁻²), and good stability, maintaining ~82% activity for seven days. Human plasma testing validated accurate glucose detection (6.05 mM), consistent with physiological levels. Overall, quaternized PVP(Q) mediators significantly improved solubility and electron transfer, enabling the development of a stable, selective glucose sensor suitable for CGM applications. Full article

Technological advances in laboratory-grown diamonds (LGDs) have eroded the scarcity premium of natural diamonds, raising the question of whether diamonds still function as a safe haven. At the same time, crystalline osmium has become investable for the first time, as crystallization technology enables safe storage, certification, and global trading. Using monthly data from 2017–2025, we form diversified portfolios with and without diamonds and with and without osmium, as well as two-asset combinations with the MSCI World. The results show that diamonds no longer provide reliable stability, while osmium consistently contributes to reducing volatility. For portfolio investors, the key lesson is that traditional safe-haven roles can change; diamonds no longer offer robust protection, whereas crystalline osmium acts as a stabilizing component. These findings illustrate the contrasting effects of technological change: substitution and loss of value for diamonds, usability and stabilization for osmium. Full article

We have developed a new bioanode based on a cascade of reactions catalyzed by two enzymes. A glassy carbon electrode is modified with β-glucosidase and glucose oxidase enzymes entrapped within an osmium redox polymer. Cellobiose, the fuel for the anode, is hydrolyzed by β-glucosidase (TxGH116), yielding two molecules of D-glucose. Glucose is then oxidized by glucose oxidase (GOx) into δ-gluconolactone and produces electrons that are transferred to the electrode mediated by osmium redox polymer. We investigated the kinetic parameters of both enzymes at different temperatures. For GOx, the effect of enzyme loading and enzyme/polymer ratio were also optimized. The proposed bioanode is coupled to a biocathode based on horseradish peroxidase (HRP) in which H₂O₂, the oxidant, is reduced. We investigated the performance of the biofuel cell on cellobiose and sugarcane hydrolysates subjected to different pretreatments. Alkaline pretreatments of biomass were found to be more effective than phosphoric acid pretreatment. Adding TxGH116 β-glucosidase further enhanced current generation, even when commercial cellulase was used. Full article

Sulfonamides represent a versatile class of biologically active compounds, best known for their antibacterial activity, but increasingly investigated for their potential in oncology. Free sulfonamides themselves display cytotoxic properties; however, coordination with metal ions often enhances both selectivity and potency, while also introducing new mechanisms of action. Although numerous studies have reported sulfonamide–metal complexes with anticancer activity, a systematic overview linking biological properties to the central metal atom has been lacking. This review summarizes current research on sulfonamide complexes with transition metals and selected main-group elements, focusing on their pharmacological potential as anticancer agents. The compounds discussed include complexes of titanium, chromium, manganese, rhenium, ruthenium, osmium, iridium, palladium, platinum, copper, silver, gold, iron, cobalt, nickel, uranium, calcium, magnesium and bismuth. For each group, representative structures are presented along with cytotoxicity data against cancer cell lines, comparisons with reference drugs such as for example cisplatin, and where relevant, studies on carbonic anhydrase inhibition. The survey of available data demonstrates that many sulfonamide–metal complexes show cytotoxic activity comparable to or greater than existing chemotherapeutic agents, while in some cases exhibiting reduced toxicity toward non-cancerous cells. These findings highlight the promise of sulfonamide–metal complexes as a fertile area for anticancer drug development and provide a framework for future design strategies. This review covers the research on anti-cancer activity of sulfonamide complexes during the years 2007–2025. Full article

Pyridyl-thiourea complexes of formula [(Cym)MCl(κ²N_py,S-H₂NNS)][SbF₆] (Cym = η⁶-p-MeC₆H₄iPr; H₂NNS = N-(p-tolyl)-N′-(2-pyridylmethyl)thiourea); M = Ru (1), Os (2)) were synthesized by reacting the corresponding metal dimers [{(Cym)MCl}₂(μ-Cl)₂] with H₂NNS in the presence of NaSbF₆. Subsequent chloride abstraction with AgSbF₆, followed by NH deprotonation using NaHCO₃, afforded the cationic complexes [(Cym)M(κ³N_py,N_amide,S-HNNS)][SbF₆] (M = Ru (5a), (5c); M = Os (6a, 6c)) and [(Cym)M(κ²N_amide,S-HNNS)][SbF₆] (M = Ru (5b); M = Os (6b)). The proposed structures for the prepared compounds are based on NMR data. Complexes 5a, 5b, and 6a, 6b evolve to the thermodynamically more stable species 5c and 6c, respectively, in which the deprotonated ligand HNNS adopts a κ³N_py,N_amide,S coordination mode. Complexes 5c and 6c activate H₂, behaving as frustrated Lewis pair (FLP) species, and catalyze (5c and/or 6c) the hydrogenation of polar multiple bonds, including the C=N bonds of N-benzylideneaniline and quinoline, the C=C bond of methyl acrylate, and the C=O bond of 2,2,2-trifluoroacetophenone. Full article