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    Membrane-based ethylene/ethane separation: The upper bound and beyond

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    Type
    Article
    Authors
    Rungta, Meha
    Zhang, Chen
    Koros, William J.
    Xu, Liren cc
    Date
    2013-08-02
    Online Publication Date
    2013-08-02
    Print Publication Date
    2013-09
    Permanent link to this record
    http://hdl.handle.net/10754/598798
    
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    Abstract
    Ethylene/ethane separation via cryogenic distillation is extremely energy-intensive, and membrane separation may provide an attractive alternative. In this paper, ethylene/ethane separation performance using polymeric membranes is summarized, and an experimental ethylene/ethane polymeric upper bound based on literature data is presented. A theoretical prediction of the ethylene/ethane upper bound is also presented, and shows good agreement with the experimental upper bound. Further, two ways to overcome the ethylene/ethane upper bound, based on increasing the sorption or diffusion selectivity, is also discussed, and a review on advanced membrane types such as facilitated transport membranes, zeolite and metal organic framework based membranes, and carbon molecular sieve membranes is presented. Of these, carbon membranes have shown the potential to surpass the polymeric ethylene/ethane upper bound performance. Furthermore, a convenient, potentially scalable method for tailoring the performance of carbon membranes for ethylene/ethane separation based on tuning the pyrolysis conditions has also been demonstrated. © 2013 American Institute of Chemical Engineers.
    Citation
    Rungta M, Zhang C, Koros WJ, Xu L (2013) Membrane-based ethylene/ethane separation: The upper bound and beyond. AIChE J 59: 3475–3489. Available: http://dx.doi.org/10.1002/aic.14105.
    Sponsors
    The authors thank The Dow Chemical Co., for funding this work. The authors especially thank Mark Brayden and Marcos Martinez for helpful discussions and comments. The authors also acknowledge additional support provided by King Abdullah University of Science and Technology (KAUST).
    Publisher
    Wiley
    Journal
    AIChE Journal
    DOI
    10.1002/aic.14105
    ae974a485f413a2113503eed53cd6c53
    10.1002/aic.14105
    Scopus Count
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