Influence of Intermolecular Interactions on the Observable Porosity in Intrinsically Microporous Polymers

被引:120
|
作者
Weber, Jens [1 ]
Du, Naiying [2 ]
Guiver, Michael D. [2 ,3 ]
机构
[1] Max Planck Inst Colloids & Interfaces, Dept Colloid Chem, D-14424 Potsdam, Germany
[2] Natl Res Council Canada, Inst Chem Proc & Environm Technol, Ottawa, ON K1A 0R6, Canada
[3] Hanyang Univ, WCU Dept Energy Engn, Seoul 133791, South Korea
关键词
FREE-VOLUME DISTRIBUTION; GAS SEPARATION; CO2; ADSORPTION; SORPTION; PIMS; TRANSPORT; NETWORKS; ROBUST; N-2; AR;
D O I
10.1021/ma101447h
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The intrinsic microporosity of hydrolyzed polymeric films was studied by means of gas sorption using nitrogen and carbon dioxide as probe molecules. X-ray scattering was used to get a better insight into the polymer microstructure. The results show that the polymer chain stiffness is not affected by the degree of hydrolysis, it can be assumed that the reduction of the size of the free-volume elements is due to chain deformations. The presence of this hysteresis points to a much denser structure compared to the initial samples. The unmodified PIM-1 exhibit microporosity as determined by nitrogen sorption at 77 K, and PIM1s modified with carboxylic acid groups did not take up nitrogen, except they were precipitated from solution. Temperature-dependent SAXS measurements show that microstructure of the carboxylated polymer films is changed upon heating.
引用
收藏
页码:1763 / 1767
页数:5
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