4.8 Article

Direct CO2 hydrogenation to light olefins over ZnZrOx mixed with hierarchically hollow SAPO-34 with rice husk as green silicon source and template

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 315, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2022.121572

Keywords

CO2 hydrogenation; Light olefins; Bifunctional catalysts; Hollow SAPO-34; Tandem catalysis

Funding

  1. National Natural Science Foundation of China [U21A20324, 21908073]
  2. Natural Science Foundation of Fujian Province [2019J01074, 2021J06026]

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In this study, a new method for preparing hollow SAPO-34 with hierarchical porous structures (referred to as bio-SAPO-34) using rice husk as a sole silicon source and porous template was presented. The bio-SAPO-34 exhibited high olefin selectivity in the methanol-to-olefins reaction. Bifunctional catalysts consisting of ZnZrOx and bio-SAPO-34 were fabricated for the direct conversion of CO2 to light olefins.
Here, we present a new preparation strategy for hollow SAPO-34 with hierarchical porous structures using rice husk as a sole silicon source and porous template (viz., bio-SAPO-34). The hollow feature and acidity amount of the bio-SAPO-34 were highly dependent on the amount of rice husk in the synthetic solutions. The bio-SAPO-34 exhibited very high olefin selectivity (94.5 %) in the methanol-to-olefins reaction. Bifunctional catalysts con-sisting of ZnZrOx and bio-SAPO-34 were fabricated for the direct conversion of CO2 to light olefins. The C-2(=)-C-4(=) selectivity of 83 % and C-2(=)-C-4(=) space-time yield of 6.14 mmol g(cat)(-1) h(-1) was achieved with only 1 % undesired CH4 at 13.8 % CO2 conversion. Particularly, the CO selectivity from the reverse water-gas shift reaction was sup-pressed to a low value (40 %). Furthermore, the in-situ DRIFTS result indicates that CH3O* is the key interme-diate forming on the ZnZrOx surface and transferring to the Bronsted acid site of bio-SAPO-34 for selective C-C coupling.

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