Ontology type: schema:ScholarlyArticle Open Access: True
2020-08-27
AUTHORSXiaolin Li, Juehua Wang, Nannan Bai, Xinran Zhang, Xue Han, Ivan da Silva, Christopher G. Morris, Shaojun Xu, Damian M. Wilary, Yinyong Sun, Yongqiang Cheng, Claire A. Murray, Chiu C. Tang, Mark D. Frogley, Gianfelice Cinque, Tristan Lowe, Haifei Zhang, Anibal J. Ramirez-Cuesta, K. Mark Thomas, Leslie W. Bolton, Sihai Yang, Martin Schröder
ABSTRACTThe 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. More... »
PAGES4280
http://scigraph.springernature.com/pub.10.1038/s41467-020-17640-4
DOIhttp://dx.doi.org/10.1038/s41467-020-17640-4
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PUBMEDhttps://www.ncbi.nlm.nih.gov/pubmed/32855396
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