Propylene production through propane dehydrogenation (PDH) is endothermic, and high temperatures required to achieve acceptable propane conversions lead to low selectivity and severe carbon-induced deactivation of conventional catalysts. We developed a catalyst-membrane system that removes the hydrogen by-product and can thus achieve propane conversions that exceed equilibrium limits. In this codesigned system, a silica/alumina (SiO/AlO) hollow-fiber hydrogen membrane was packed with a selective platinum-tin (PtSn/SiO) PDH catalyst on the tube side with hydrogen diffusing from the tube to the shell side. We demonstrate that the catalyst-membrane system can achieve propane conversions >140% of the nominal equilibrium conversion with a propylene selectivity >98% without deactivation of the system components. We also show that by introducing oxygen on the shell side of the catalyst-membrane system, we can couple the endothermic PDH reaction on the tube side with exothermic hydrogen oxidation on the shell side. This coupling results in higher rates of hydrogen transport, leading to further enhancements in the propane conversion as well as desired thermoneutral system operation.
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http://dx.doi.org/10.1126/science.adh3712 | DOI Listing |
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January 2025
Department of Chemistry and Life Science, Yokohama National University, Yokohama, 240-8501, Japan.
Hydrogen spillover, particularly when involving "interparticle" hydrogen spillover, offers a unique opportunity to enhance catalytic efficiency by remote activation of surface acidity. Building on this concept, this study aims to investigate physically mixed alumina-supported platinum nanoparticles (Pt/AlO) and zirconia-supported tungsten oxide (WO/ZrO) in promoting the direct synthesis of cumene from benzene and propane at 300 °C. The reaction with Pt/AlO alone afforded propylene as the only product, indicating the successive reaction route of Pt-catalyzed dehydrogenation of propane, followed by acid-catalyzed alkylation.
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
State Key Laboratory of Fine Chemicals, Liaoning Key Laboratory for Catalytic Conversion of Carbon Resources, School of Chemistry, Dalian University of Technology, Dalian 116024, China.
Metal-free boron-based materials exhibit remarkable performance in oxidative dehydrogenation of propane (ODHP). Rational design of boron-based catalysts requires a systematic understanding of the underlying mechanisms to constitute a knowledge base. This work provides a comprehensive view of the reaction mechanism of the boron-based ODH reaction and discusses the key features of the reaction systems, including the inhibition of deep oxidation, high olefin selectivity, and the role of water in the ODHP reaction.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
University of Michigan, Department of Electrical Engineering and Computer Science, UNITED STATES OF AMERICA.
The photocatalytic nonoxidative coupling of methane (PNOCM) offers a promising route to synthesize valuable C2+ hydrocarbons while minimizing side reactions. Oxide-based photocatalysts have been predominant in this field, but suffering from limited conversion rates, selectivity, and durability due to poor C-C coupling as well as overoxidation of CH4 by lattice oxygen. Here, we introduce an advancement in PNOCM for methane conversion into ethane and propane using GaN, one of the most produced semiconductors, together with trace amounts of metallic cobalt clusters (0.
View Article and Find Full Text PDFAdv Mater
January 2025
Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
The direct dehydrogenation of alkanes to olefins under mild conditions is challenging due to the inert nature of alkyl C─H bonds. Herein, an efficient photocatalytic system is developed for propane direct dehydrogenation (PDH) to propylene, consisting of ≈1.30 nm sized PtO clusters immobilized on a layered double hydroxide -derived ZnO/AlO support (LD-Pt).
View Article and Find Full Text PDFAdv Mater
January 2025
School of Chemistry and Chemical Engineering, Ministry of Education Key Laboratory of Special Functional Aggregated Materials, Shandong Key Laboratory of Advanced Organosilicon Materials and Technologies, Shandong University, Jinan, 250100, China.
SnO₂ is a widely used electron transport layer (ETL) material in perovskite solar cells (PSCs), and its design and optimization are essential for achieving efficient and stable PSCs. In this study, the in situ formation of a chain entanglement gel polymer electrolyte is reported in an aqueous phase, integrated with SnO₂ as the ETL. Based on the self-polymerization of 3-[[2-(methacryloyloxy)ethyl]dimethylammonium]propane-1-sulfonic acid (DAES) in an aqueous environment, combining the catalytic effect of LiCl (as a Lewis acid) with the salting-out effect, and the introduction of polyvinylpyrrolidone (PVP) as the other polymer chain, a chain entanglement gelled SnO (G-SnO) structure is successfully constructed with a wide range of functions.
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