Nickel silicate beta zeolite prepared by interzeolite transformation: A highly active and stable catalyst for dry reforming of methane
[Display omitted] •Hydrothermal interzeolite transformation of nickel silicate MWW to *BEA zeolite.•Novel synthesis of nickel silicate beta zeolite using bottom-up method.•In-situ formation of highly dispersed metallic nickel clusters in Ni-BEA.•Highly active and stable Ni catalyst for dry reforming...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2022-03, Vol.431, p.133364, Article 133364 |
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Format: | Artikel |
Sprache: | eng |
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•Hydrothermal interzeolite transformation of nickel silicate MWW to *BEA zeolite.•Novel synthesis of nickel silicate beta zeolite using bottom-up method.•In-situ formation of highly dispersed metallic nickel clusters in Ni-BEA.•Highly active and stable Ni catalyst for dry reforming of methane.•Platform technique for the preparation of zeolite-metal composite.
The preparation of porous nickel silicates has received considerable attention because of its potential as a catalyst for various applications, such as dry reforming of methane (DRM), CO2 hydrogenation, and water–gas shift. In this study, we first synthesize the nickel silicate *BEA-type zeolite (Ni-BEA) via the interzeolite transformation of nickel silicate MWW within 12 h. The presence of Ni in the tetrahedral framework of the *BEA structure is experimentally demonstrated using diverse analytical methods. The extraction of framework Ni at high temperatures generates uniform metallic Ni clusters within the pores of the *BEA structure. Ni-BEA exhibits the highest conversions of CH4 and CO2 and stability for DRM among the employed catalysts owing to the significant quantity of highly dispersed Ni clusters in the three-dimensional large-pore system. The synthesis of metallosilicate *BEA by interzeolite transformation and in-situ generation of uniform metal clusters can be expanded to the other metal-zeolite catalysts. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2021.133364 |