One-of-A-Kind: A Microporous Metal-Organic Framework Capable of Adsorptive Separation of Linear, Mono- and Di-branched Alkane Isomers via Temperature- and Adsorbate-Dependent Molecular Sieving
KAUST DepartmentAdvanced Membranes and Porous Materials Research Center
Chemical Science Program
Nanostructured Functional Materials (NFM) laboratory
Physical Science and Engineering (PSE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/627528
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AbstractSeparation of alkane isomers represents a crucial process in the petrochemical industry in order to achieve high octane rating of gasoline. Herein, we report the first example of complete separation of linear, monobranched and dibranched alkane isomers by a single adsorbent. A calcium-based robust microporous metal-organic framework, Ca(H2tcpb) (tcpb = 1,2,4,5-tetrakis(4-carboxyphenyl)-benzene) exhibits unique molecular exclusion behavior which enables full separation of binary or ternary mixtures of alkane isomers into pure form of each isomerate. The successful separation of monobranched and dibranched hexane isomers will not only lead to the production of higher quality gasoline with maximum possible octane numbers but also fill the gap in the current separation technology. Exploration of separation mechanism indicates that structural flexibility and adsorbate-dependent structure change of the porous framework plays a vital role for the observed temperature-dependent molecular sieving property of the adsorbent.
CitationWang H, Dong X, Velasco E, Olson DH, Han Y, et al. (2018) One-of-a-kind: a microporous metal–organic framework capable of adsorptive separation of linear, mono- and di-branched alkane isomers via temperature- and adsorbate-dependent molecular sieving. Energy & Environmental Science. Available: http://dx.doi.org/10.1039/c8ee00459e.
SponsorsWe would like to thank the financial support from the Materials Sciences and Engineering Division, Office of Basic Research Energy Sciences of the U.S. Department of Energy through Grant No. DE-FG02-08ER-46491. Y.H. acknowledges the KAUST CCF fund for supporting part of this study.
PublisherRoyal Society of Chemistry (RSC)
JournalEnergy & Environmental Science