Journal
POLYMER
Volume 219, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2021.123538
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Funding
- Strategic High Technology Innovation Fund of the Chinese Academy of Sciences [CXJJ-19-B06]
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This study investigated the effects of thermal annealing on gas separation performance of two 6FDA-DETDA/DMMDA block polyimide membranes with different block lengths at three temperatures. The results showed that the 350 degrees C annealing significantly enhanced the gas separation performance of the membranes.
Block polymers with thermal annealing are attractive routes to produce 6FDA-based polyimide membranes with enhanced gas separation performance. However, some 6FDA-based polyimide membranes exhibit different gas separation behavior trends under the thermal annealing process. In this work, two 6FDA-DETDA/DMMDA block polyimide membranes with different 6FDA-DETDA block lengths were prepared and annealed at three temperatures (150 degrees C, 250 degrees C and 350 degrees C). To investigate the thermal annealing process and its influence on the thermal cross-linking behavior and aggregation structures, in situ XRD and ambient-pressure Xray photoelectron spectroscopy (AP-XPS) were employed. Based on the orbital-weighted Fukui function calculated by Time-dependent density functional theory (TDDFT) and AP-XPS spectra, it's found that free radicals cross-linking that induced by 350 degrees C annealing occurred in imide rings, and resulted in the destroyed imide rings and decreased average interchain distances in both block polyimides. However, the massive 6FDA-DETDA block hindered imide rings from destruction and resulted in a slight molecular filtration, which benefited the gas transport of small kinetic diameter gases. As a result, 350 degrees C annealed membrane of bPI-2 exhibited enhanced gas separation performance. We expect that this work will shed light on the effect of thermal annealing on the gas separation behavior of block polyimides and offer a way to tune gas separation performance by thermal annealing.
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