Issue 42, 2023

Surface engineering on a microporous metal–organic framework to boost ethane/ethylene separation under humid conditions

Abstract

Recently, examples of metal–organic frameworks (MOFs) have been identified displaying ethane (C2H6) over ethylene (C2H4) adsorption selectivity. However, it remains a challenge to construct MOFs with both large C2H6 adsorption capacity and high C2H6/C2H4 adsorption selectivity, especially under humid conditions. Herein, we reported two isoreticular MOF-5 analogues (JNU-6 and JNU-6-CH3) and their potential applications in one-step separation of C2H4 from C2H6/C2H4 mixtures. The introduction of CH3 groups not only reduces the pore size from 5.4 Å in JNU-6 to 4.1 Å in JNU-6-CH3 but also renders an increased electron density on the pyrazolate N atoms of the organic linker. JNU-6-CH3 retains its framework integrity even after being immersed in water for six months. More importantly, it exhibits large C2H6 adsorption capacity (4.63 mmol g−1) and high C2H6/C2H4 adsorption selectivity (1.67) due to the optimized pore size and surface function. Breakthrough experiments on JNU-6-CH3 demonstrate that C2H4 can be directly separated from C2H6/C2H4 (50/50, v/v) mixtures, affording benchmark productivity of 22.06 and 18.71 L kg−1 of high-purity C2H4 (≥99.95%) under dry and humid conditions, respectively.

Graphical abstract: Surface engineering on a microporous metal–organic framework to boost ethane/ethylene separation under humid conditions

Supplementary files

Article information

Article type
Edge Article
Submitted
07 Aug 2023
Accepted
08 Oct 2023
First published
09 Oct 2023
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2023,14, 11890-11895

Surface engineering on a microporous metal–organic framework to boost ethane/ethylene separation under humid conditions

X. Xie, Y. Wang, Q. Cao, R. Krishna, H. Zeng, W. Lu and D. Li, Chem. Sci., 2023, 14, 11890 DOI: 10.1039/D3SC04119K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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