Search Results (535)

This paper analyzes the operation of a spark-ignition reciprocating engine fueled by purified landfill gas (LFG). The engine serves as the prime mover for an electric generator and a heat source within a Combined Heat and Power (CHP) unit. Experimental data is retrieved from the Engine Control Unit (ECU). The findings encompass 3000 operating hours (September–December), a period characterized by evolving spark plug conditions, during which various adjustments and service tasks are performed. This study primarily addresses operational strategies for spark plug maintenance to guarantee CHP system reliability, with a specific focus on electrode degradation and its subsequent effect on engine performance. A significant portion of the research analyzes the wear of eight OEM spark plugs installed during the observation period. Utilizing data from a specific interval (4044 to 4797 h), the study calculates the wear rates for both center and ground electrodes based on volume loss measurements obtained via digital microscopy. The results indicate varied electrode wear across the set. Furthermore, the correlation between spark plug condition, misfire counts, emergency shutdowns, and service intervals is examined. The misfires counter is proposed as a parameter for predicting emergency shutdowns and as an indicator for spark plug adjustment or replacement. Lastly, the paper describes potential causes of accelerated ground electrode wear and suggests probable methods for enhancing component longevity. Full article

To investigate the structural characteristics of Ir_n clusters (n = 9–30) and their interaction with NH₃, the CALYPSO structure-prediction method was employed to identify the lowest-energy configurations. The Lennard–Jones potential was then used to compute the binding energy and average binding energy, thereby evaluating size-dependent stability. The results show that Ir_n clusters evolve from relatively open motifs to compact three-dimensional frameworks as n increases. Meanwhile, the average binding energy increases overall and exhibits several locally stable size regions, indicating a pronounced size effect. Based on slab and cluster models, NH₃ adsorption was further examined on the Ir₁₃ cluster as a representative system due to its high structural stability as a “magic-number” cluster. The calculated adsorption energies demonstrate that the Ir₁₃ cluster exhibits substantially stronger adsorption than the bulk Ir surface, with low-coordinated Ir atoms playing a key role in strengthening the interaction and enhancing adsorption activity. Adsorption-configuration analysis indicates that NH₃ preferentially binds to active surface sites via the N lone pair. These findings clarify the relationship between structural stability and adsorption performance of Ir clusters and provide theoretical support for Ir-based materials in NH₃ catalytic conversion and high-sensitivity gas detection, and offer insights relevant to improving NH₃ monitoring in underground coal mine environments. Full article

Nonsteroidal anti-inflammatory drugs such as phenylbutazone (PBZ) are among the most widely used medications globally due to their effectiveness in relieving pain and reducing inflammation. This study aims to detect PBZ with metallic particle-based electrochemical sensors using cyclic voltammetry (CV) in the presence of catechol as a redox probe. The approach focuses on evaluating the electrochemical behaviour of PBZ under different experimental conditions and optimizing the detection parameters to develop a simple, rapid, and cost-effective analytical method suitable for this pharmaceutical compound in lab practice. CV was performed using four types of screen-printed electrodes, each modified with different transitional metal particles, in potassium ferrocyanide/potassium ferricyanide, catechol, and catechol-PBZ solutions to study the electrochemical response and detection capability for PBZ. The best performance characteristics were obtained for the sensor modified with Ir particles that detect PBZ, with a linearity range of 0.01 to 1.00 μM and a detection limit of 1.53 nM. Additionally, Fourier-transform infrared spectroscopy (FT-IR) was used to characterize the PBZ in pharmaceuticals. The method using an iridium-modified sensor developed in this study allows the accurate detection of PBZ in pharmaceuticals with a relative error lower than 4%. Full article

Nanoparticle powders of a Ce_1−xRu_xO₂ mixed oxide (3.0% w/w), were synthesized to be used as catalytic supports, on which Pt and Ir nanoparticles were deposited as the active phase. The catalytic supports were prepared through a route involving microwave heating, while the Pt or Ir nanoparticles were incorporated via the wet incipient method. The {Pt, Ir/Ce_1−xRu_xO₂} catalytic systems were successfully tested as catalysts for low-temperature CO oxidation. To provide adequate support to our results, the compounds were characterized by SEM, EDS, XRD, DRS-UV-vis, and XPS techniques. In addition, BET isotherms were carried out to determine specific surface area features. The CO oxidation evolution was tested in the range of 25–350 °C. Both Pt and Ir supported Ce_1−xRu_xO₂ catalysts that remarkably improved the CO oxidation, reaching and sustaining 100% conversion from 125 °C onwards. Remarkably, the mixed oxide support, by itself, showed outstanding performance, achieving 100% conversion to CO₂, at a temperature of 225 °C. Full article

Developing active and robust catalysts for the acidic oxygen evolution reaction (OER) with reduced Ir loading is still a challenge in the industrial production of green H₂. In this work, several catalysts ranging from single metal oxides (e.g., IrO₂) to high-entropy oxides (IrNiMnFeCoCuVO_x) were synthesised through thermal decomposition in air to study the effect of the mixed-oxide composition in terms of activity and stability towards the acidic OER. Catalysts were named MOx-n, with n being the number of metal elements in the mixture. The results show that the activity of rutile IrO₂ can be improved by introducing other elements into the composition. The best performance was obtained for MOx-4 to MOx-5, which delivered a current density of 10 mA cm⁻² at an overpotential (η₁₀) of 279 ± 4 mV; approx. 100 mV lower than IrO₂ at a comparable Ir loading and with better stability. Nevertheless, further increasing the complexity of the mixed oxide resulted in an evident degradation in terms of activity and stability. It is worth noting that surface dissolution and reconstruction occurred with all mixed-oxide catalysts, including high-entropy configurations. Full article

To develop high-performance iridium phosphorescent complexes, we designed and synthesized a series of iridium phosphorescent complexes (G-1, G-2, B-1, B-2, R-1, R-2) using 3-hydroxy-2-methyl-4-pyrone (maltol, short for mal) and 3-hydroxy-2-ethyl-4-pyrone (ethyl maltol, short for emal) as auxiliary ligands, in combination with 2-phenylpyridine (ppy), 2-(2,4-difluorophenyl)pyridine (dfppy), and 1-phenylisoquinoline (piq) as cyclometalating ligands. We systematically investigated their crystal structures, photophysical behavior, electrochemical properties, and electroluminescent performance. The results revealed that the combination of a pyranone auxiliary ligand with the highly conjugated piq ligand leads to the formation of R-1 and R-2, which possess high molecular symmetry and display favorable photophysical performance. These complexes exhibit solution-phase phosphorescence quantum yields of 64% and 55%, and electroluminescent devices incorporating them reach a maximum external quantum efficiency of 13.4%, with brightness exceeding 13,000 cd/m² and minimal efficiency roll-off. In contrast, complexes incorporating pyridine-based cyclometalating ligands (ppy, dfppy)—G-1, G-2, B-1, and B-2—display weak emission in solution but show enhanced solid-state emission through π–π stacking, with a maximum quantum yield of 25.8%. Density functional theory calculations and electrochemical analysis indicate that the presence of both the pyranone auxiliary ligand and the piq ligand results in optimized frontier orbital energy alignment, enhanced metal-to-ligand charge transfer, and reduced non-radiative transitions, thereby improving emission efficiency. This study provides a theoretical framework and molecular design strategy for the application of pyranone auxiliary ligands in high-performance iridium phosphorescent materials. Full article

The reaction mechanism of the gold-catalyzed hydrothiolation of alkenes (1) with thiols (2) has been investigated in detail. The tetranuclear gold complex, (PPh₃)₄Au₄(SPh)₂(NTf)₂ (A), is a key intermediate in the catalytic hydrothiolation of alkenes. It forms instantaneously when PPh₃AuNTf₂ and PhSH are mixed in THF. Monitoring the reaction over time using ³¹P NMR spectroscopy revealed that gold complex A remained stable in the reaction system throughout the hydrothiolation process. In addition, we successfully observed a rapid ligand-exchange reaction between the thiolate group of gold complex A and thiols in solution. The gold-catalyzed alkene hydrothiolation reaction has been applied to the catalytic hydrothiolation of allenes, which have degenerate double bonds. Hydrothiolation of allenes proceeded regioselectively at the terminal double bond. However, the yield was lower than that observed for alkenes, and catalyst deactivation occurred. The hydrothiolation products of allenes were difficult to detach from the gold catalyst, necessitating an increase in the reaction temperature. Since high periodic transition metals such as gold and platinum are effective for hydrothiolation of alkenes and allenes, it is interesting to clarify whether iridium complexes, which belong to the same period as gold and platinum, could also catalyze alkene hydrothiolation. Through a detailed investigation of iridium ligands and reaction conditions, it was found that, in iridium systems, disulfide formation via oxidative coupling of thiols occurs preferentially over hydrothiolation reactions. This is likely due to steric hindrance around the iridium center, which inhibits alkene coordination to the iridium. Additionally, the hydrothiolation proceeding at low yields is believed to be a radical reaction involving electron transfer through the iridium complex. Full article

Selective laser melting (SLM) is a complex additive manufacturing process involving rapid laser–material interaction, steep thermal gradients, and phase change phenomena. In this work, a two-dimensional thermal model based on the lattice Boltzmann method (LBM) is developed to simulate the SLM process of AlSi10Mg and 316L stainless steel (316L SS) alloys. The model captures the laser–material interaction, layer-by-layer deposition, phase change behavior, and heat transfer mechanisms, including conduction and convection. Experimental observations of melt pool width and depth were also performed on the microstructures of the two SLM alloys in order to compare the results with the numerical predictions. For the AlSi10Mg alloy, good agreement is obtained, with relative errors of 19.13% in melt pool width and 7.58% in depth, accurately capturing melt pool penetration and remelting behavior. In contrast, moderate deviations are observed for 316L SS, indicating a higher sensitivity to thermophysical properties and suggesting that further model refinement is required. Overall, the results demonstrate the capability of the LBM framework as an efficient and robust tool for analyzing thermal behavior in SLM and for supporting process parameter optimization. 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

Catalytic materials are central to the advancement of hydrogen generation technologies, playing a pivotal role in enabling sustainable, carbon-neutral energy systems. Hydrogen can be produced via electrochemical water splitting, thermochemical reforming, or photocatalysis—each imposing unique performance requirements on catalysts in terms of activity, selectivity, stability, and efficiency. While traditional noble metals (e.g., platinum, ruthenium, iridium) provide benchmark catalytic activity, their widespread use is hindered by scarcity, high cost, and limited long-term durability. Consequently, researchers have increasingly focused on earth-abundant alternatives such as transition metals (Ni, Co, Fe, Mo), alloys, metal oxides, carbides, sulfides, nitrides, and carbon-based systems. Among these, two-dimensional materials, particularly the MXene family, have attracted significant attention due to their metallic conductivity, layered structure, and tunable surface chemistry. These features enable rapid charge transfer and abundant active sites, making MXenes and related nanostructured catalysts promising for both the Hydrogen Evolution Reaction (HER) and Oxygen Evolution Reaction (OER) across a wide range of electrochemical conditions. Parallel efforts have integrated novel semiconductors, plasmonic nanomaterials, and hybrid heterostructures to improve the efficiency of solar-to-hydrogen energy conversion. This paper reviews the main types of catalytic materials used in hydrogen production, explains their design strategies and structure–performance relationships, and discusses key engineering challenges such as integrating renewable energy sources, scaling up manufacturing, and ensuring long-term durability in real-world systems. Future research goals are also highlighted, including the development of affordable non-noble catalysts, enhancing catalyst stability through surface and defect engineering, and coupling hydrogen production with circular economy principles, all of which are essential to making hydrogen generation more efficient, scalable, and cost-effective as the world transitions to clean and sustainable energy. Full article

Background/Objectives: Brachytherapy (BT) is a local radiation treatment method for solid tumors. A single 10 Gy high–dose–rate (HDR) BT acts as an “in situ” vaccination. Tumor microenvironment (TME)–dependent radio–resistance mechanisms, such as increasing immunosuppression and hypoxia, lead to tumor recurrence after radiotherapy. Our study aimed to determine whether adding imiquimod (IMQ) to anticancer therapy would overcome TME–mediated mechanisms of radiotherapy resistance. IMQ, a toll–like receptor 7 (TLR7) agonist, acts as an immunostimulant and a vascular normalizing agent. Methods: Mice with well–developed tumors were treated with IMQ at a vascular–normalized dose of 50 μg, followed 5 days later by a single 10 Gy HDR BT. The dose coverage was planned using Discovery RT computed tomography CT scans. Irradiation was performed with a high–dose–rate afterloader equipped with an iridium–192 radioactive source. Results: In mice treated with a combination of IMQ and BT, we observed significant inhibition of melanoma tumor growth. We also noticed an effective therapeutic effect in mice with breast cancer, resulting in significantly prolonged survival and complete tumor regression in 20% of treated mice. In the blood of treated mice, we observed leukopenia with eosinophilia. In tumors, there was enhanced infiltration by cytotoxic CD8⁺ T lymphocytes. The depletion of CD8⁺ T cells completely abolished the effect of the combined therapy. Conclusions: The combination of IMQ with HDR brachytherapy induces a synergistic effect, improving the therapeutic antitumor effect of brachytherapy. Our data indicate that it is reasonable to use drugs that prevent changes in the TME in combination with radiotherapy. Full article

Noble metal-catalyzed C–H activation has transformed synthetic methodology by enabling direct modification of inert C–H bonds with high levels of efficiency, selectivity, and functional group tolerance. This mini-review provides a focused overview of the mechanistic foundations and emerging advances in C–H functionalization mediated by ruthenium, iridium, rhodium and palladium catalysts. Key activation modes including oxidative addition, concerted metalation deprotonation (CMD), and electrophilic pathways are discussed alongside the roles of high-valent intermediates and ligand control in determining reactivity and regioselectivity. Special emphasis is placed on recent electrochemical strategies, where anodic oxidation replaces traditional chemical oxidants, granting access to unique redox manifolds and expanding the scope of C–C, C–N, C–O, and C–X bond-forming reactions. Representative transformations highlight the versatility of noble metals in constructing heterocycles, enabling enantioselective processes, and facilitating late-stage functionalization of complex molecules. Current challenges and future perspectives are outlined, including the need for improved nondirected activation, deeper mechanistic insight, and enhanced scalability. Collectively, this review underscores the central role of noble metals in advancing sustainable and innovative C–H functionalization chemistry. Full article

The proliferation of Low Earth Orbit (LEO) satellite constellations, driven by the NewSpace economy and reduced launch costs, has opened new opportunities for positioning, navigation, and timing (PNT) applications. Compared to traditional GNSS systems operating in Medium Earth Orbit, LEO satellites offer several advantages: higher received signal power, better satellite geometry and visibility in urban environments, and greater Doppler dynamics—enabling approaches such as single-satellite and Doppler-based positioning. Although dedicated LEO-PNT constellations are still under development, existing commercial LEO satellites can already be leveraged for experimental positioning applications. This paper presents a portable, multi-constellation testbed built using commercial off-the-shelf (COTS) hardware and software-defined radio (SDR) technologies. The platform enables the synchronous acquisition and processing of LEO signals from Orbcomm, Iridium, and Starlink, allowing for the extraction of key positioning observables. A comprehensive measurement campaign is conducted across both indoor and outdoor environments to evaluate signal visibility and Doppler tracking performance. Results highlight the potential of opportunistic LEO-based positioning, particularly in challenging scenarios such as indoor environments where traditional GNSS solutions are unreliable. 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

Electrocatalytic hydrogenation (ECH) represents an environmentally friendly pathway for converting 5-hydroxymethylfurfural (HMF) into the high-value chemical 2,5-bis(hydroxymethyl)furan (BHMF). However, its selectivity and Faradaic efficiency are often constrained by competitive hydrogen evolution at the cathode and insufficient supply of active hydrogen at the surface. To address this challenge, this study developed an Ir-decorated copper oxide nanowire catalyst (denoted as CuIr) featuring a hydrogen-rich adsorption (H_ads) surface. The incorporation of Ir significantly enhances the catalyst’s water dissociation capacity, creating abundant H_ads sources that selectively accelerate HMF hydrogenation while suppressing side reactions. Under a mild applied potential of −0.45 V vs. RHE and a current density of approximately −20 mA cm⁻², the optimal CuIr₄₀ catalyst achieved near-complete conversion of HMF (99%), a BHMF yield of 99%, and a high Faradaic efficiency of 97% within 120 min of electrolysis. Mechanistic studies reveal that this catalytic leap stems from the synergistic functional interaction between Cu and Ir sites in substrate activation and hydrogen supply. This work presents a novel strategy for designing efficient electrocatalysts for biomass hydrogenation by regulating surface H_ads concentration. Full article