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Highly selective, high capacity separation of o-xylene from C8 aromatics by a switching adsorbent layered material

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posted on 2019-05-22, 13:49 authored by Shi-Qiang Wang, Soumya Mukherjee, Ewa Patyk-Kaźmierczak, Shaza DarwishShaza Darwish, Alankriti Bajpai, Qing‐Yuan Yang, Michael J. Zaworotko
Purification of the C8 aromatics (xylenes and ethylbenzene) is particularly challenging because of their similar physical properties. It is also relevant because of their industrial utility. Physisorptive separation of C8 aromatics has long been suggested as an energy efficient solution but no physisorbent has yet combined high selectivity (>5) with high adsorption capacity (>50 wt %). Now a counterintuitive approach to the adsorptive separation of o‐xylene from other C8 aromatics involves the study of a known nonporous layered material, [Co(bipy)2(NCS)2]n (sql‐1‐Co‐NCS), which can reversibly switch to C8 aromatics loaded phases with different switching pressures and kinetics, manifesting benchmark o‐xylene selectivity (SOX/EB≈60) and high saturation capacity (>80 wt %). Structural insight into the observed selectivity and capacity is gained by analysis of the crystal structures of C8 aromatics loaded phases.

Funding

Investigation of the triple mutual system Li, Ba // BO2, F and the growth of bulk crystals of b-BaB2O4

Russian Foundation for Basic Research

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History

Publication

Angewandte Chemie;20 (3), pp. 6630-6634

Publisher

Wiley and Sons Ltd.,

Note

peer-reviewed

Other Funding information

SFI

Rights

This is the author accepted peer reviewed version of the following article: Highly selective, high capacity separation of o-xylene from C8 aromatics by a switching adsorbent layered material, Angewandte Chemie, 2019, 58 (20), pp. 6630-6634 which has been published in final form at https://doi.org/10.1002/anie.201901198 This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. http://olabout.wiley.com/WileyCDA/Section/id-828039.html#terms

Language

English

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