Reduction process is a key step to fabricate metal-zeolite catalysts in catalytic synthesis. However, because of the strong interaction force, metal oxides in zeolites are very difficult to be reduced. Existing reduction technologies are always energy-intensive, and inevitably cause the agglomeration of metallic particles in metal-zeolite catalysts or destroy zeolite structure in severe cases. Herein, we disclose that zeolites after ion exchange of ammonium have an interesting and unexpected self-reducing feature. It can accurately control the reduction of metal-zeolite catalysts, via in situ ammonia production from 'ammonia pools', meanwhile, restrains the growth of the size of metals. Such new and reliable ammonia pool effect is not influenced by topological structures of zeolites, and works well on reducible metals. The ammonia pool effect is ultimately attributed to an atmosphere-confined self-regulation mechanism. This methodology will significantly promote the fabrication for metal-zeolite catalysts, and further facilitate design and development of low-cost and high-activity catalysts.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8854602PMC
http://dx.doi.org/10.1038/s41467-022-28606-zDOI Listing

Publication Analysis

Top Keywords

metal-zeolite catalysts
16
ammonia pool
8
catalysts
5
ammonia
4
ammonia pools
4
zeolites
4
pools zeolites
4
zeolites direct
4
direct fabrication
4
fabrication catalytic
4

Similar Publications

Selectivity control by zeolites during methanol-mediated CO hydrogenation processes.

Chem Soc Rev

January 2025

Interdisciplinary Institute of NMR and Molecular Sciences, School of Chemistry and Chemical Engineering, The State Key Laboratory of Refractories and Metallurgy, Hubei Province for Coal Conversion and New Carbon Materials, Wuhan University of Science and Technology, Wuhan 430081, P. R. China.

The thermocatalytic conversion of CO with green or blue hydrogen into valuable energy and commodity chemicals such as alcohols, olefins, and aromatics emerges as one of the most promising strategies for mitigating global warming concerns in the future. This process can follow either a CO-modified Fischer-Tropsch synthesis route or a methanol-mediated route, with the latter being favored for its high product selectivity beyond the Anderson-Schulz-Flory distribution. Despite the progress of the CO-led methanol-mediated route over bifunctional metal/zeolite catalysts, challenges persist in developing catalysts with both high activity and selectivity due to the complexity of CO hydrogenation reaction networks and the difficulty in controlling C-O bond activation and C-C bond coupling on multiple active sites within zeolites.

View Article and Find Full Text PDF

Hierarchical zeolite-encapsulated metal nanoparticles for heterogeneous catalysis.

Nanoscale

November 2024

Laboratory for Catalysis Engineering, School of Chemical and Biomolecular Engineering, Sydney Nano Institute, the University of Sydney, NSW 2006, Australia.

Zeolites, characterized by their highly porous structure, have become integral to modern industry and environmental science due to their broad applications in adsorption, separation, and catalysis. Recent advancements in zeolite synthesis, particularly through hydrothermal methods and the incorporation of metal nanoparticles, have significantly expanded their utility. This review delves into the innovative strategies for encapsulating metal nanoparticles within zeolite matrices, enhancing catalytic reactions' efficiency, selectivity, and durability.

View Article and Find Full Text PDF

Stability and Dynamics of Zeolite-Confined Gold Nanoclusters.

J Chem Theory Comput

September 2024

Department of Chemical Engineering, University of California, Davis, Davis, California 95616, United States.

Nanoengineered metal@zeolite materials have recently emerged as a promising class of catalysts for several industrially relevant reactions. These materials, which consist of small transition metal nanoclusters confined within three-dimensional zeolite pores, are interesting because they show higher stability and better sintering resistance under reaction conditions. While several such hybrid catalysts have been reported experimentally, key questions such as the impact of the zeolite frameworks on the properties of the metal clusters are not well understood.

View Article and Find Full Text PDF

Under the background of the continuous rise of CO annual emissions, the development of CO capture and utilization technology is urgent. This study focuses on improving the catalytic capacity of the catalyst for CO hydrogenation, improving the efficiency of CO conversion to methanol, and converting H into chemical substances to avoid the danger of H storage. Based on the concept of element sharing, the ASMZ (Aluminum Shares Metal Zeolite catalysts) series catalyst was prepared by combining the CuO-ZnO-AlO catalyst with the ZSM-5 zeolite using the amphoteric metal properties of the Al element.

View Article and Find Full Text PDF

Selective Upcycling of Polyethylene over Ru/H-ZSM-5 Bifunctional Catalyst into High-Quality Liquid Fuel at Mild Conditions.

ChemSusChem

October 2024

Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang, 110016, Liaoning, China.

It has been known that plastics with undegradability and long half-times have caused serious environmental and ecological issues. Considering the devastating effects, the development of efficient plastic upcycling technologies with low energy consumption is absolutely imperative. Catalytic hydrogenolysis of single-use polyethylene over Ru-based catalysts to produce high-quality liquid fuel has been one of the current top priority strategies, but it is restricted by some tough challenges, such as the tendency towards methanation resulting from terminal C-C cleavage.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!