原位
膜
化学
基质(化学分析)
化学工程
色谱法
有机化学
生物化学
工程类
作者
Yueyangchao Yu,Yanting Tang,Longjie Liu,Qingnan Wang,Chongshan Yin,Keming Zhang,Chenlu Liu,Yi Ye,Xinglei Zhao,Tingting Gu,Shaofei Wang
标识
DOI:10.1021/acs.iecr.5c00266
摘要
Covalent organic frameworks (COFs) show exceptional promise for CO2-selective mixed matrix membranes (MMMs) due to their tunable porosity and structural robustness. To mitigate COF aggregation in MMMs, we present an in situ growth strategy by directly integrating COF precursors into a polymer matrix. By optimizing reaction conditions, we achieve uniform dispersion and successful in situ formation of TpPa (derived from 1,3,5-triformylphloroglucinol and p-phenylenediamine) within the Pebax matrix. The optimized membrane exhibits a high CO2 permeability of 313.4 Barrer (45.8% higher than pure Pebax) and CO2/N2 selectivity of 22.6, along with long-term stability. Positron annihilation lifetime spectroscopy further reveals how the integration of COFs modulates the membrane’s free-volume properties. This study not only addresses filler dispersion challenges but also provides a viable approach for fabricating high-performance, stable CO2 separation membranes.
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