Li, Xiaolin, Wang, Juehua, Bai, Nannan, Zhang, Xinran, Han, Xue, da Silva, Ivan, Morris, Christopher G., Xu, Shaojun, Wilary, Damian M., Sun, Yinyong, Cheng, Yongqiang, Murray, Claire A., Tang, Chiu C., Frogley, Mark D., Cinque, Gianfelice, Lowe, Tristan, Zhang, Haifei, Ramirez-Cuesta, Anibal J., Thomas, K. Mark, Bolton, Leslie W., Yang, Sihai and Schröder, Martin
2020.
Refinement of pore size at sub-angstrom precision in robust metal-organic frameworks for separation of xylenes.
Nature Communications
11
(1)
, 4280.
10.1038/s41467-020-17640-4
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Abstract
The demand for xylenes is projected to increase over the coming decades. The separation of xylene isomers, particularly p- and m-xylenes, is vital for the production of numerous polymers and materials. However, current state-of-the-art separation is based upon fractional crystallisation at 220 K which is highly energy intensive. Here, we report the discrimination of xylene isomers via refinement of the pore size in a series of porous metal–organic frameworks, MFM-300, at sub-angstrom precision leading to the optimal kinetic separation of all three xylene isomers at room temperature. The exceptional performance of MFM-300 for xylene separation is confirmed by dynamic ternary breakthrough experiments. In-depth structural and vibrational investigations using synchrotron X-ray diffraction and terahertz spectroscopy define the underlying host–guest interactions that give rise to the observed selectivity (p-xylene < o-xylene < m-xylene) and separation factors of 4.6–18 for p- and m-xylenes.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Chemistry Cardiff Catalysis Institute (CCI) |
Additional Information: | This article is licensed under a Creative Commons Attribution 4.0 International License |
Publisher: | Nature Research |
ISSN: | 2041-1723 |
Date of First Compliant Deposit: | 10 March 2021 |
Date of Acceptance: | 6 July 2020 |
Last Modified: | 05 May 2023 02:34 |
URI: | https://orca.cardiff.ac.uk/id/eprint/139574 |
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