Search Results (549)

The microstructure, phase composition, and high-temperature oxidation behavior of Al_0.5CoCr_0.5NiPt_0.1 and AlCoCr_0.5NiPt_0.1 multi-principal element alloys (MPEAs) at 1100 °C in air were investigated. Depending on the content of aluminum, the microstructure of as-cast samples contains FCC and BCC solid solutions. Similarly, the ratio of two solid solutions varies depending on the aluminum content in the alloy. When the content of aluminum is x = 0.5, the microstructure is dominated by the FCC solid solution, while a BCC solid solution is dominated when the concentration of aluminum is increased to x = 1.0. Moreover, in both MPEAs, platinum exists as a part of solid solutions rather than a separate phase. High-temperature oxidation was carried out in a Plavka.Pro PM-1 SmartKiln muffle furnace under isothermal conditions at 1100 °C for 100 h exposure in air, and weighing was performed every 10 h. The maximum specific weight gain for the Al_0.5CoCr_0.5NiPt_0.1 alloy was 0.965 mg/cm², and 0.675 mg/cm² for the AlCoCr_0.5NiPt_0.1 alloy. Based on the high-temperature oxidation experiment results, it was established that AlCoCr_0.5NiPt_0.1 MPEA exhibits greater resistance towards high-temperature dry air corrosion with the formation of an exclusive Al₂O₃ scale on the surface with 3–5 μm thickness; the parabolic oxidation rate constant for this alloy is k_p = 20.2 × 10^–13 (g²/cm⁴s). Introduction of platinum into the composition of the Fe-free AlCoCr_0.5Ni alloy reduces the value of the parabolic oxidation rate constant by half. Full article

Two mineral-based solid residues, namely coal gangue (CG) and phosphorus tailings (PT), two of the largest solid waste streams in the mining industry, were used as the sole metal feedstocks to fabricate a novel MgCaFeAl layered double hydroxide (LDH-GT) via a 700 °C calcination, acid leaching and hydrothermal coprecipitation route, with simultaneous synthesis of white carbon black from the reaction byproducts. Under optimized conditions (total metal load is 150 mg kg⁻¹, LDH-GT dose is 0.09 g, pH from 6 to 7), the synthesized material achieved concurrent immobilization efficiencies of 76.28%, 99.96%, and 99.95% for Cr (VI), Cd (II) and Ni (II), respectively, within a 24 h reaction period. TCLP leachability decreased by 82 to 91% relative to the untreated soil. After three wetting, drying and freeze–thaw cycles, the leached concentrations of all three metals remained below 0.3 mg L⁻¹, confirming excellent long-term stability. Mechanistic analyses revealed that Cr (VI) was mainly sequestered through interlayer anion exchange and surface complexation, whereas Cd (II) and Ni (II) were immobilized via isomorphic substitution into the LDH lattice, precipitation as carbonates, and incorporation into Fe/Mn oxides. A 7-day mung bean bioassay showed that LDH-GT amendment increased seed germination from 50% to 73%, enhanced root and shoot biomass by 1.1- to 1.6-fold, and decreased plant Cr, Cd, and Ni contents by over 80%. The 16S rRNA sequencing further demonstrated that LDH-GT reversed the decline in microbial α diversity induced by heavy metal stress, restored aerobic chemoheterotrophic and sulfur cycling functional guilds, and reduced pathogenic signatures. This study provides the demonstration of a waste-to-resource LDH that achieves efficient, durable remediation of multi-metal-contaminated soils, offering a scalable route for coupling solid waste valorization with in situ site restoration. Full article

Achieving selective conversion of lignin-derived phenolic compounds to cycloalkanes under mild conditions remains a significant challenge. Herein, we report a novel iron-incorporated two-dimensional NiO nanosheet supported Pd-Pt alloy catalyst (Pd_1.7-Pt_0.3/NiO-5FeO_x) that is capable of facilitating highly efficient hydrodeoxygenation (HDO) of lignin-derived phenolic model compounds (e.g., 2,6-dimethoxy-4-methylphenol) under mild conditions (250 °C, 5 atm H₂). The reaction mechanism was investigated through various characterization techniques and mechanistic studies: introducing FeO_x into the NiO support increases the proportion of defect-related oxygen species (Oβ), enhances adsorption of the key hydrogenated alcohol intermediate 4-methylcyclohexanol, and optimizes the acidity distribution of the catalyst, thereby promoting C(_sp³)-O bond cleavage (dehydroxylation) toward cycloalkane formation. The catalyst achieved high conversion (>95%) for various lignin-derived phenolics and high selectivity (93.0%) toward methylcyclohexane under mild conditions. This work offers new insights into the design of efficient biomass conversion catalysts under mild conditions and provides an energy-efficient route for the sustainable utilization of lignin resources. Full article

To overcome active site blockage and poor interfacial contact in traditional syntheses, PtNi bimetallic nanoparticles were grown in situ on a microporous carbon paper via pulse electrodeposition. Firstly, the impact of deposition potential was investigated. The results indicate that the deposition potential significantly modulates the surface Pt⁰/Pt²⁺ ratio; concurrently, a shift toward more negative potentials intensified nanoparticle agglomeration. The effects of the duty cycle were investigated at an optimal deposition potential of −0.95 to −0.4 V. A duty cycle of 30% yielded the optimal Pt⁰/Pt²⁺ ratio. Furthermore, TEM revealed a coexisting strain profile of bulk PtNi lattice contraction and localized expansion at peripheral Pt (111) facets. This synergistic tuning of surface valence and strain optimizes the thermodynamic balance between oxygen adsorption and intermediate desorption on Pt sites. In summary, the optimal catalyst, prepared at a deposition potential of −0.95 V and a duty cycle of 30%, showed the best reaction behavior in the oxygen reduction reaction with an initial onset potential of 0.92 V (vs. RHE). After 5000 cycles of testing, the catalyst showed a constant durability, with the onset potential degrading only marginally to 0.87 V. This work successfully demonstrates that the surface morphology and valence states of the catalyst can be effectively tailored by regulating the pulse voltage and duty cycle. 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

It is necessary to find sustainable alternatives to the conventional fossil fuels used by the transportation sector today. For the hard-to-abate aviation and heavy transport, liquid hydrocarbon fuels derived from biomass via pyrolysis are a viable option. Biomass pyrolysis oils need upgrading by hydroprocessing before they can be further processed into fuels at a refinery. Due to reactor plugging and catalyst deactivation in one-step hydroprocessing, it has been proposed to add a stabilization step at a lower temperature to convert the most reactive compounds in pyrolysis oil, such as carbonyls, to less reactive species such as alcohols. Three different catalysts, Ni/Al₂O₃, sulfided NiMo/Al₂O₃, and Pt/Al₂O₃, were studied for stabilizing three different model compounds, furfural, guaiacol, and octanoic acid, alone and as a mixture in a batch reactor at 90 bar initial H₂ pressure and 180 °C. The order of performance was determined to be Ni/Al₂O₃ > Pt/Al₂O₃ > sulfided NiMo/Al₂O₃ in these conditions. The Ni/Al₂O₃ catalyst showed both the highest overall conversion, the most fully hydrogenated compounds, and the highest carbonyl conversion. The effect of adding 1172 wt-ppm sulfur to the feed was also investigated, which showed that Ni/Al₂O₃ was the most sensitive catalyst to sulfur poisoning. Full article

Background: Invasive Aspergillosis (IA) is a rare but life-threatening fungal infection in immunocompromised hosts, including solid organ transplant (SOT) recipients. While extensively studied in other SOT populations, data on IA in pancreas transplant (PT) recipients are limited. Earlier studies reported mortality rates nearing 100%, whereas more recent data show that 12-week mortality still exceeds 20% despite improvements in antifungal therapy. Current prophylaxis strategies for PT recipients mainly focus on Candida species, and there are no clear, standardized recommendations for Aspergillus prevention. Given the paucity of focused data, the epidemiology, clinical characteristics, and outcomes of IA in PT recipients are not well defined. This study aimed to assess the incidence, clinical characteristics, and outcomes of IA among hospitalized PT patients using a nationally representative dataset. Methods: We conducted a descriptive analysis using the National Inpatient Sample (NIS) from 2016 to 2020. PT admissions were identified using International Classification of Diseases, Tenth Revision (ICD 10) codes for transplant status and procedures. IA was defined using validated ICD 10 codes. Baseline demographics, hospital characteristics, comorbidities, and outcomes, including sepsis, acute kidney injury (AKI), acute respiratory failure (ARF), invasive mechanical ventilation (IMV), all-cause in-hospital mortality, length of stay, and total hospitalization costs and charges were compared between PT admissions with and without IA. National estimates were calculated using discharge weights, and comparisons were performed using the chi-square test and adjusted Wald test. Multivariable analysis was performed to identify predictors of all-cause in-hospital mortality among PT admissions complicated by IA. Two-sided p values < 0.05 were considered statistically significant. Results: Between 2016 and 2020, 65,980 PT-related hospitalizations were identified, of which 250 (0.4%) had IA. PT admissions complicated by IA were more commonly aged 41 to 60 years (59% vs. 46%, p = 0.012) and were less likely to have a Charlson Comorbidity Index greater than 3 (54% vs. 68.6%, p < 0.001) compared with PT hospitalizations without IA. The PT with the IA cohort had higher rates of sepsis (100% vs. 46.1%, p < 0.001), AKI (60% vs. 36.7%, p < 0.001), ARF (28% vs. 9.4%, p < 0.001), and IMV use (18% vs. 4%, p < 0.001) compared with the PT without the IA cohort. Among PT hospitalizations with IA, IMV use was independently associated with higher all-cause in-hospital mortality (adjusted odds ratio 48.777, p = 0.009). Overall, in-hospital mortality was significantly higher in PT hospitalizations with IA compared with those without IA (12% vs. 2%, p < 0.001). Mean length of stay was longer (24.86 vs. 6.13 days, p < 0.001), and total charges ($378,494 vs. $94,938, p < 0.001), and total costs ($93,019 vs. $24,463, p = 0.023) were significantly higher compared with PT hospitalizations without IA. Conclusion: Although rare, IA in PT recipients is associated with higher rates of sepsis, AKI, ARF, venous thromboembolism, prolonged hospitalization, increased mortality, and greater healthcare utilization. Despite the inherent limitations of administrative datasets, this nationally representative analysis highlights the substantial clinical and economic burden of IA in this high-risk population. These findings emphasize the need for targeted surveillance, early diagnosis, and evidence-based antifungal strategies in this vulnerable population. Full article

This review analyzes the catalytic routes for the Power-to-X (PtX) conversion of hydrogen to methane, methanol, ammonia, formic acid, and synthetic hydrocarbon fuels. The key reactive synthesis technologies and catalysts for each vector are described. Recent studies and pilot projects summarizing the reaction pathways of each vector and the associated catalyst technologies are also discussed. The analysis indicates that catalyst selection critically influences the efficiency and selectivity of these reactive systems. Some catalyst synthesis routes rely on expensive critical minerals (e.g., Ru and Rh), which raise technical and economic challenges for their industrial application. Catalyst deactivation and scale-up limitations are also relevant issues to be resolved. Emerging catalysts (e.g., Fe–Co or Co–Ni bimetallics, core–shell materials, metal-organic frameworks (MOFs), electrides, covalent-organic frameworks (COFs), and perovskites) are being explored to enhance stability, selectivity, and deactivation. Europe leads PtX development to consolidate the industrial production of hydrogen-based vectors with strong policy support, while the industrial initiatives in Latin America are limited (for instance, Chile’s green methanol and ammonia projects are examples) despite its great potential to generate renewable energy. In summary, Power-to-X can store renewable energy and close the carbon loop; however, its industrial consolidation demands catalyst innovation and supportive regulatory frameworks to overcome the challenges highlighted in this review. Full article

The rapid growth of electronic waste (e-waste) demands sustainable recovery solutions based on green chemistry. Conventional recycling relies on energy-intensive pyrometallurgical routes that cause emissions and material losses. This study applies Molecular Recognition Technology™ (MRT™) for selective energy-efficient recovery of base (Cu, Ni, Fe, Sn) and precious/platinum group metals (Ag, Pd, Pt) from a collector metal alloy. A hydrometallurgical process combining electrowinning, sequential acid leaching, and MRT™ separations achieved >99% metal purity with minimal waste generation. The results demonstrate MRT™ as a scalable green alternative for high-efficiency metal recovery from e-waste, supporting circular economy objectives. Full article

Platinum group metals (PGMs) are strategic metals, and recycling PGMs in spent automobile exhaust catalysts (SACs) is a key path to alleviate the contradiction between resource supply and demand. This paper proposes a new Cu-Ni capture process and conducts research on the recovery of PGMs from SACs. Through the binary phase diagram analysis of Cu, Ni and PGMs and the thermodynamic calculation of the system reduction reaction, the feasibility of this technology was theoretically confirmed. Experimental results show that under the conditions of a temperature of 1450 °C, a holding time of 90 min, a Cu-Ni ratio of 1:1, and a basicity of 0.58, the recovery rates of Pt, Pd, and Rh reached 99.2%, 99.34%, and 98.48% respectively. Combined with orthogonal experiments, it was verified that temperature is the most influential factor on the recovery rate, and the four-stage capture mechanism of “initial diffusion—droplet aggregation—sedimentation and wetting—slag–metal separation” was clarified. This process reduces the melting temperature and provides new technology for green and efficient recycling of PGMs. Full article

This study investigates reduced graphene oxide (rGO)-supported bimetallic M–Pt (M = Co, Ni, Cu) alloy nanoparticles as electrocatalysts for the hydrogen evolution reaction (HER) in alkaline media. Monometallic Pt and bimetallic M–Pt nanoparticles were synthesized and uniformly dispersed on rGO, followed by structural and compositional characterization using transmission electron microscopy and inductively coupled plasma mass spectrometry. Their electrocatalytic performance toward HER was systematically evaluated at different temperatures. All electrocatalysts exhibited enhanced activity at higher temperatures, with current densities increasing by approximately 1.68–2.65 times at 338 K compared with 298 K. Among the investigated materials, CoPt/rGO delivered the highest cathodic current densities and a Tafel slope of 75 mV dec⁻¹, indicating favorable reaction kinetics. This performance is associated with a higher electroactive surface area, as determined by cyclic voltammetry, and reduced charge-transfer resistance, as revealed by electrochemical impedance spectroscopy. Notably, the CoPt/rGO electrocatalyst demonstrated excellent short-term operational stability at a constant potential of −0.28 V vs. RHE. These results highlight the potential of rGO-supported CoPt bimetallic alloys as efficient electrocatalysts for alkaline water electrolysis. Full article

The oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are two processes that occur during the operation of the cathodic electrode in Zn–Air batteries, which enable the integration of alternative energy sources into electrical energy distribution systems. Transition metal oxides, such as perovskites based on LaNiO₃, are promising electrocatalysts for the ORR and OER in alkaline medium due to their versatile structure, allowing for the substitution of certain atoms with dopants, which enhances the catalytic activity for both reactions. This work reports an electrochemical study of the catalytic activity toward ORR and OER of perovskite catalysts (LaNiO3 doped with transition metals (Fe, Mn, or Pd)) in the presence of carbon-based materials as supports (multiwalled carbon nanotubes (MWCNT), graphene oxide nanosheets (GO), and graphitic carbon (C)). The results revealed interesting catalytic properties in both reactions, particularly La(Ni_0.9Pd_0.1)O₃/MWCNT, which showed an ORR activation potential of 0.87 V vs. RHE, comparable to that of the commercial Pt/C catalyst (0.99 V vs. RHE), while the overpotential for OER was lower than that of the Pt/C catalyst (1.68 V vs. RHE for La(Ni_0.9Pd_0.1)O₃/MWCNT and 1.79 V vs. RHE for the commercial Pt/C). Full article

Underwater electrical explosions of single metallic wires driven by microsecond current pulses are investigated and compared with previously reported sub-microsecond experiments. Current and voltage waveforms, streak camera shadow imaging, and one-dimensional hydrodynamic simulations are employed to characterize how the energy density, energy density deposition rate, and the generated shock waves in water depend on the wire parameters. It was found that, similar to the sub-microsecond timescale, the solid–liquid phase transition occurs later than thermodynamic calculations predicted, while the liquid–vapor phase transition happens sooner than expected, leading to a two-phase coexistence. Additionally, most materials show a notable resistance peak (Ti, Fe, Ni, Zn, Ag, Sn, Ta, Au) compared to a quasi-plateau for Cu and Mo or a continuous increase for Al and Pt. Moreover, the specific action integral values are significantly smaller than those observed in wire explosion experiments in vacuum. Finally, the plasma formed at peak resistive voltage is non-ideal but exhibits lower electron density, ionization degree, and temperature compared to the sub-microsecond case. Full article

The current work examines the impact of isopropanol (IPA) on the electrochemical characteristics of nickel foam and Pd-modified Ni foam electrodes in a 0.1 M NaOH medium, with respect to the kinetics of the hydrogen evolution reaction (HER) over the temperature range of 20–40 °C. Comparative HER/IPA examinations are presented for a highly catalytic polycrystalline Pt electrode. Electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and cathodic Tafel polarization experiments were carried out in this work, where the IPA concentrations ranged from 1.0 × 10⁻⁵ to 1.0 × 10⁻³ M. The introduction of small amounts of isopropyl alcohol into the working electrolyte noticeably facilitated the catalytic efficiency of the hydrogen evolution reaction on the surface of Ni foam electrodes. This is most likely related to the fact that IPA molecules undergo partial electrooxidation to acetone (qualitatively confirmed by GC-MS analysis) during initial CV cycling, which is believed to significantly diminish the surface tension phenomenon during the HER, thus promoting hydrogen bubble separation from the electrode surface. It should also be noted that acetone will continuously be produced at the Pt anode, making it essential to consider further migration of (CH₃)₂CO molecules to the working cell compartment. Most importantly, isopropanol was found not to undergo significant surface electrosorption on the nickel foam-based catalysts, which could otherwise significantly inhibit the hydrogen evolution reaction On the contrary, the presence of IPA in the electrolyte solution seems to have a detrimental effect on the kinetics of both the HER and the UPDH (underpotential deposition of H) processes on the surface of the polycrystalline Pt electrode, which is a superior electrochemical catalyst for HER, but highly susceptible to surface contamination. Full article

This paper demonstrates the results of constructive technological research on the development of a catalyst with a Ni/PSi@Pt structure. This catalyst eliminates the use of gold in the structure of μ-FC electrodes. This work uses the main technological solutions for the formation of a gold-containing “core–shell” structure on the inner surface of pores. Comparative data on the results of assessing the durability of porous silicon electrodes with both Pt catalysts and composite catalysts of the Pt/In₂O₃, Pt/SnO₂, Pt/Au and Pt/Ni types are also presented. Full article