Role of intrachain rigidity in the plasticization of intrinsically microporous triptycene-based polyimide membranes in mixed-Gas CO2/CH4 separations
KAUST DepartmentAdvanced Membranes and Porous Materials Research Center
Physical Sciences and Engineering (PSE) Division
Chemical and Biological Engineering Program
Permanent link to this recordhttp://hdl.handle.net/10754/563851
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AbstractBased on high-pressure pure- and mixed-gas (50:50) CO2/CH4 separation properties of two intrinsically microporous triptycene-based polyimides (TPDA-TMPD and TPDA-6FpDA), the intrachain rigidity central to "conventional PIM" design principles is not a singular solution to intrinsic plasticization resistance. Despite the significant intrachain rigidity in TPDA-TMPD, a 300% increase in PMIX(CH4), 50% decrease in α(CO2/CH4) from 24 to 12, and continuous increase in PMIX(CO2) occurred from 4 to 30 bar. On the other hand, the more flexible and densely packed TPDA-6FpDA exhibited a slight upturn in PMIX(CO2) at 20 bar similar to a dense cellulose acetate (CA) film, also reported here, despite a 4-fold higher CO2 sorption capacity. Microstructural investigations suggest that the interconnected O2- and H2-sieving ultramicroporosity of TPDA-TMPD is more sensitive to slight CO2-induced dilations and is the physical basis for a more extensive and accelerated plasticization. Interchain rigidity, potentially by interchain interactions, is emphasized and may be facilitated by intrachain mobility.
SponsorsThe authors acknowledge financial support of this work by KAUST funding for Prof. Ingo Pinnau.
PublisherAmerican Chemical Society (ACS)