Selective Ethane/Ethylene Separation in a Robust Microporous Hydrogen-Bonded Organic Framework

Authors
  • X. Zhang
  • L. Li
  • J.-X. Wang
  • H.-M. Wen
  • R. Krishna
  • H. Wu
  • W. Zhou
  • Z.-N. Chen
  • B. Li
  • G. Qian
  • B. Chen
Publication date 08-01-2020
Journal Journal of the American Chemical Society
Volume | Issue number 142 | 1
Pages (from-to) 633-640
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
Abstract
The separation of ethane (C2H6) from ethylene (C2H4) is of prime importance in the production of polymer-grade C2H4 for industrial manufacturing. It is very challenging and still remains unexploited to fully realize efficient C2H6/C2H4 separation in the emerging hydrogen-bonded organic frameworks (HOFs) due to the weak nature of hydrogen bonds. We herein report the benchmark example of a novel ultrarobust HOF adsorbent (termed as HOF-76a) with a Brunauer-Emmett-Teller surface area exceeding 1100 m2 g-1, exhibiting the preferential binding of C2H6 over C2H4 and thus highly selective separation of C2H6/C2H4. Theoretical calculations indicate the key role of the nonpolar surface and the suitable triangular channel-like pores in HOF-76a to sterically "match'' better with the nonplanar C2H6 molecule than the planar C2H4, thus affording overall stronger multipoint van der Waals interactions with C2H6. The exceptional separation performance of HOF-76a for C2H6/C2H4 separation was clearly demonstrated by gas adsorption isotherms, ideal adsorbed solution theory calculations, and simulated and experimental breakthrough curves. Breakthrough experiments on HOF-76a reveal that polymer-grade ethylene gas can be straightforwardly produced from 50/50 (v/v) C2H6/C2H4 mixtures during the first adsorption cycle with a high productivity of 7.2 L/kg at 298 K and 1.01 bar and 18.8 L/kg at 298 K and 5.0 bar, respectively.
Document type Article
Note With Supporting Information
Language English
Related dataset CCDC 1907797: Experimental Crystal Structure Determination
Published at https://doi.org/10.1021/jacs.9b12428
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