Temperature-Dependent Gas Transport Behavior in Cross-Linked Liquid Crystalline Polyacrylate Membranes

dc.contributor.authorRabie, Ferasen
dc.contributor.authorPoláková, Lenkaen
dc.contributor.authorFallas, Sebastianen
dc.contributor.authorSedlakova, Zdenkaen
dc.contributor.authorMarand, Evaen
dc.contributor.authorMartin, Stephen M.en
dc.contributor.departmentChemical Engineeringen
dc.date.accessioned2019-08-23T11:58:44Zen
dc.date.available2019-08-23T11:58:44Zen
dc.date.issued2019-08-20en
dc.date.updated2019-08-23T07:04:04Zen
dc.description.abstractStable, cross-linked, liquid crystalline polymer (LCP) films for membrane separation applications have been fabricated from the mesogenic monomer 11-(4-cyanobiphenyl-4&prime;-yloxy) undecyl methacrylate (CNBPh), non-mesogenic monomer 2-ethylhexyl acrylate (2-EHA), and cross-linker ethylene glycol dimethacrylate (EGDMA) using an in-situ free radical polymerization technique with UV initiation. The phase behavior of the LCP membranes was characterized using differential scanning calorimetry (DSC) and X-ray scattering, and indicated the formation of a nematic liquid crystalline (LC) phase above the glass transition temperature. The single gas transport behavior of CO<sub>2</sub>, CH<sub>4</sub>, propane, and propylene in the cross-linked LCP membranes was investigated for a range of temperatures in the LC mesophase and the isotropic phase. Solubility of the gases was dependent not only on the condensability in the LC mesophase, but also on favorable molecular interactions of penetrant gas molecules exhibiting a charge separation, such as CO<sub>2</sub> and propylene, with the ordered polar mesogenic side chains of the LCP. Selectivities for various gas pairs generally decreased with increasing temperature and were discontinuous across the nematic&ndash;sotropic transition. Sorption behavior of CO<sub>2</sub> and propylene exhibited a significant change due to a decrease in favorable intermolecular interactions in the disordered isotropic phase. Higher cross-link densities in the membrane generally led to decreased selectivity at low temperatures when the main chain motion was limited by the lack of mesogen mobility in the ordered nematic phase. However, at higher temperatures, increasing the cross-link density increased selectivity as the cross-links acted to limit chain mobility. Mixed gas permeation measurements for propylene and propane showed close agreement with the results of the single gas permeation experiments.en
dc.description.versionPublished versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationRabie, F.; Poláková, L.; Fallas, S.; Sedlakova, Z.; Marand, E.; Martin, S.M. Temperature-Dependent Gas Transport Behavior in Cross-Linked Liquid Crystalline Polyacrylate Membranes. Membranes 2019, 9, 104.en
dc.identifier.doihttps://doi.org/10.3390/membranes9080104en
dc.identifier.urihttp://hdl.handle.net/10919/93230en
dc.language.isoenen
dc.publisherMDPIen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subjectliquid crystal polymeren
dc.subjectmembraneen
dc.subjectpermeabilityen
dc.subjectnematicen
dc.subjectgas separationen
dc.titleTemperature-Dependent Gas Transport Behavior in Cross-Linked Liquid Crystalline Polyacrylate Membranesen
dc.title.serialMembranesen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten

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