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Low-molecular-weight poly(ethylene glycol) (PEG) is deliberately incorporated into synthesized swellable poly(ethylene oxide) (PEO) membranes via a facile post-treatment strategy. The membranes exhibit both larger fractional free volume (FFV) and a higher content of CO2-philic building units, resulting in significant increments in both CO2 permeability and CO2/H2 selectivity. The separation performance correlates nicely with the microstructure of the membranes. This study may provide useful insights in the formation and mass transport behavior of highly efficient polymeric membranes applicable to clean energy purification and CO2 capture, and possibly bridge the material-induced technology gap between academia and industry. [ABSTRACT FROM AUTHOR]

The microstructural evolution of a series of triazine framework-based microporous (TFM) membranes under different conditions has been explored in this work. The pristine TFM membrane is in situ fabricated in the course of polymer synthesis via a facile Brønsted-acid-catalyzed cyclotrimerizaiton reaction. The as-synthesized polymer exhibits a microporous network with high thermal stability. The free volume size of the TFM membranes gradually evolved from a unimodal distribution to a bimodal distribution under annealing, as analyzed by positron annihilation lifetime spectroscopy (PALS). The emergence of the bimodal distribution is probably ascribed to the synergetic effect of quenching and thermal cyclization reaction. In addition, the fractional free volume (FFV) of the membranes presents a concave trend with increasing annealing temperature. Vapor sorption tests reveal that the mass transport properties are closely associated with the free volume evolution, which provides an optimal condition for dehydration of biofuels. A promising separation performance with extremely high water permeability has been attained for dehydration of an 85 wt % ethanol aqueous solution at 45 °C. The study on the free volume evolution of the TFM membranes may provide useful insights about the microstructure and mass transport behavior of the microporous polymeric materials. [ABSTRACT FROM AUTHOR]

A novel sulfonated polyphenylsulfone (sPPSU)/polyphenylsulfone (PPSU)-based dual-layer hollow fiber membrane with a nanometric thin skin layer has been designed for biofuel dehydration via pervaporation. The thickness of skin selective layer is in the range of 15-90 nm under different spinning conditions measured by positron annihilation spectroscopy (PAS) coupled with a mono-energetic positron beam. The effects of outer-layer dope properties, coagulation temperature, and dope flow rate during spinning were systematically investigated. By tuning these spinning parameters, a high performance sPPSU/PPSU-based dual-layer hollow fiber membrane with desirable morphology was successfully obtained. Particularly owing to its nanometric thin skin layer, a high flux of 3.47 kg/m2h with a separation factor of 156 was achieved for dehydration of an 85 wt % isopropanol aqueous solution at 50°C. After post thermal treatment at 150°C for 2 h, the separation factor was dramatically improved to 687 while flux dropped to 2.30 kg/m2h, which make it comparable to the inorganic membranes. In addition, excellent correlations were found among the results from field emission scanning electron microscopy, PAS spectra, and separation performance. © 2013 American Institute of Chemical Engineers AIChE J, 59: 2943-2956, 2013 [ABSTRACT FROM AUTHOR]