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The catalytic combustion of methane (CCM) has been extensively studied owing to the wide use of methane in motor vehicles and power generation turbines. However, the absence of polarizability and the high C-H bond strength are considered to be the main drawbacks that limit its oxidation by traditional catalytic converters. Palladium-based catalysts are recognized as the benchmark catalysts for methane oxidation, especially under oxidizing conditions, and their activity is dependent on different parameters such as size, dispersion, and the nature of the support. Additionally, metal oxides are the most common supports used for CCM; however, they can become saturated with water, especially during steady-state operation at low temperatures, owing to their hydrophilic nature. This causes saturation of the active sites with OH species, which poisons the active centers of the catalyst, prevents activation of methane molecules, and induces catalyst sintering. Herein, we reported the synthesis of a binary palladium nanoalloy on a halloysite nanotube support (PdM@Hal). This one-pot synthesis procedure was performed ultrasound-enhanced reduction of metal precursors in aqueous solution containing dispersed halloysite nanotubes, using NaBH as reducing agent. Transmission electron microscopy revealed that the synthesized PdM@Hal catalysts preserved the morphology of the pristine support after synthesis and calcination, with good dispersion of the catalyst on the surface of the support. Promoted metal-support interactions revealed enhanced catalytic performance, following the order PdNi > PdCo > Pd > PdCu, with activation energies of 68-94 kJ mol.
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http://dx.doi.org/10.1039/c9ra06804j | DOI Listing |
J Am Chem Soc
September 2025
Institute of Integrated Research, Institute of Science Tokyo, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.
Upgrading methane to value-added chemicals is significant but still challenging. Well-designed catalysts are required to activate methane. Extensive efforts have been dedicated to the catalytic conversion of methane over transition-metal-containing catalysts.
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
State Key Joint Laboratory of Environment Simulation and Pollution Control, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
The rapid growth of natural-gas vehicles (NGVs) necessitates robust catalysts for the simultaneous abatement of methane (CH), nitrogen oxides (NO), and carbon monoxide (CO) under fluctuating exhaust compositions. We reported a site-engineered MnGa@In-CHA OXZEO catalyst in which indium was confined within an SSZ-13 framework, and GaO and MnO phases were uniformly dispersed on its exterior. MnO markedly enhanced redox capacity, driving NO → NO oxidation and lowering the activation energy for C-H bond cleavage in CH, while GaO tuned the Brønsted acidity and mediated electron transfer among In, Mn, and Ga centers.
View Article and Find Full Text PDFInorg Chem
September 2025
Department of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 7610001, Israel.
The low-temperature oxidation of alkanes and arenes using molecular oxygen under ambient conditions is still one of the grand challenges of catalysis. Inspired by the alkane hydroxylation activity of the copper-based metalloenzyme, particulate methane monooxygenase, a tetra-copper polyoxometalate, [Cu(HO)(PWO)], was investigated as an electrocatalyst for the cathodic (reductive) oxidation of hydrocarbons with emphasis on oxidation of ethane. Controlled potential electrolysis (CPE) in water at -0.
View Article and Find Full Text PDFChemSusChem
September 2025
Soochow Institute for Energy and Materials Innovations (SIEMIS), Key Laboratory of Advanced Carbon Materials and Wearable Energy Technologies of Jiangsu Province, College of Energy, Soochow University, Suzhou, 215006, P. R. China.
The electrochemical reduction of CO to CH offers a promising pathway for renewable energy storage, yet remains limited by sluggish kinetics, poor catalyst stability, and competing hydrogen evolution reactions (HER). Herein, a host-guest strategy is reported for engineering metal-organic frameworks (MOFs) through the encapsulation of conductive polymers to stabilize reticular skeletons and regulate interfacial water for efficient CO-to-CH conversion. Specifically, polypyrrole (PPy) and polyaniline (PANI) are confined within Cu-anchored UiO-67 frameworks, resulting in hybrid catalysts-PPy@Cu-UiO-67 and PANI@Cu-UiO-67-with preserved crystallinity and enhanced electronic conductivity.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
Chemoselective borylation of methane offers a promising route to organoboron synthesis. We report a porous zirconium UiO-MOF confined mononuclear iron(III) dihydride catalyst enabling efficient monoborylation of CH using HBpin at 185 °C to afford methyl boronic acid pinacol ester in 85% yield with a cumulative TON of up to 921.
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