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  • 标题:Encapsulation of CuO nanoparticles within silicalite-1 as a regenerative catalyst for transfer hydrogenation of furfural
  • 本地全文:下载
  • 作者:Mingwei Weng ; Zihao Zhang ; Francis Okejiri
  • 期刊名称:iScience
  • 印刷版ISSN:2589-0042
  • 出版年度:2021
  • 卷号:24
  • 期号:8
  • 页码:1-14
  • DOI:10.1016/j.isci.2021.102884
  • 语种:English
  • 出版社:Elsevier
  • 摘要:SummaryCatalytic transfer hydrogenation (CTH) of biomass-derived furfural (FAL) to furfuryl alcohol is recognized as one of the most versatile techniques for biomass valorization. However, the irreversible sintering of metal sites under the high-temperature reaction or during the coke removal regeneration process poses a serious concern. Herein, we present a silicalite-1-confined ultrasmall CuO structure (CuO@silicalite-1) and then compared its catalytic efficiency against conventional surface-supported CuO structure (CuO/silicalite-1) toward CTF of FAL with alcohols. Characterization results revealed that CuO nanoparticles encapsulated within the silicalite-1 matrix are ∼1.3 nm in size in CuO@silicalite-1, exhibiting better dispersion as compared to that in the CuO/silicalite-1. The CuO@silicalite-1, as a result, exhibited nearly 100-fold higher Cu-mass-based activity than the CuO/silicalite-1 counterpart. More importantly, the activity of the CuO@silicalite-1 catalyst can be regenerated via facile calcination to remove the surface-bound carbon deposits, unlike the CuO/silicalite-1 that suffered severe deactivation after use and cannot be effectively regenerated.Graphical abstractDisplay OmittedHighlights•Ultrasmall CuO NPs are encapsulated in silicalite-1 matrix for CTH of furfural•Encapsulated CuO catalyst shows impressive Cu-mass-based activity of ∼130 hr−1•Carbon deposits can be easily removed without the obvious increase in CuO size•Strong Cu-Si interactions exist in silicalite-1-encapsulated CuO structureChemistry; Inorganic chemistry; Chemical reaction; Catalysis; Materials science
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