4.8 Article

Design of a Small Organic Template for the Synthesis of Self-Pillared Pentasil Zeolite Nanosheets

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 144, Issue 14, Pages 6270-6277

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c12338

Keywords

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Funding

  1. Fundamental Research Funds for the Central Universities [2021QNA4028]
  2. National Natural Science Foundation of China [22172141, 21802121, 21835002, 92045303, 21720102001]
  3. Shanghai Tech University [EM02161943]

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This study presents the successful synthesis of zeolite nanosheets with excellent mass transfer using a small organic template. The nanosheets exhibit good crystallinity, large surface area, and unique morphology, and show higher propylene selectivity and longer reaction lifetime in the methanol-to-propylene conversion reaction compared to conventional zeolites.
Zeolite nanosheets with excellent mass transfer are attractive, but their successful syntheses are normally resulted from a huge number of experiments. Here, we show the design of a small organic template for the synthesis of self-pillared pentasil (SPP) zeolite nanosheets from theoretical calculations in interaction energies between organic templates and pentasil zeolite skeletons. As expected, the SPP zeolite nanosheets with the thickness at 10-20 nm have been synthesized successfully. Characterizations show that the SPP zeolite nanosheets with about 90% MFI and 10% MEL structures have good crystallinity, the house-of-card morphology, large surface area, and fully four-coordinated aluminum species. More importantly, methanol-to-propylene tests show that the SPP zeolite nanosheets exhibit much higher propylene selectivity and longer reaction lifetime than conventional ZSM-5 zeolite. These results offer a good opportunity to develop highly efficient zeolite catalysts in the future.

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