Carbon molecular sieve membrane from a microporous spirobisindane-based polyimide precursor with enhanced ethylene/ethane mixed-gas selectivity
KAUST DepartmentAdvanced Membranes and Porous Materials Research Center
Chemical Engineering Program
Chemical Science Program
Nanostructured Functional Materials (NFM) laboratory
Physical Science and Engineering (PSE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/622717
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AbstractEthylene is typically produced by steam cracking of various hydrocarbon feedstocks. The gaseous products are then separated in a demethanizer followed by a deethanizer unit and finally sent to a C splitter for the final purification step. Cryogenic distillation of ethylene from ethane is the most energy-intensive unit operation process in the chemical industry. Therefore, the development of more energy-efficient processes for ethylene purification is highly desirable. Membrane-based separation has been proposed as an alternative option for replacement or debottlenecking of C splitters but current polymer membrane materials exhibit insufficient mixed-gas CH/CH selectivity (<7) to be technically and economically attractive. In this work, a highly selective carbon molecular sieve (CMS) membrane derived from a novel spirobisindane-based polyimide of intrinsic microporosity (PIM-6FDA) was developed and characterized. PIM-6FDA showed a single-stage degradation process under an inert nitrogen atmosphere which commenced at ∼480 °C. The CMS formed by pyrolysis at 800 °C had a diffusion/size-sieving-controlled morphology with a mixed-gas (50% CH/50% CH) ethylene/ethane selectivity of 15.6 at 20 bar feed pressure at 35 °C. The mixed-gas ethylene/ethane selectivity is the highest reported value for CMS-type membranes to date.
CitationSalinas O, Ma X, Wang Y, Han Y, Pinnau I (2017) Carbon molecular sieve membrane from a microporous spirobisindane-based polyimide precursor with enhanced ethylene/ethane mixed-gas selectivity. RSC Adv 7: 3265–3272. Available: http://dx.doi.org/10.1039/c6ra24699k.
SponsorsThe work reported in this publication was supported by funding from King Abdullah University of Science and Technology (KAUST).
PublisherRoyal Society of Chemistry (RSC)
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