Triptycene-based copolyimides with tailored backbone rigidity for enhanced gas transport

被引:35
作者
Weidman, Jennifer R. [1 ]
Luo, Shuangjiang [1 ]
Breier, Jaclyn M. [1 ]
Buckley, Patrick [1 ]
Gao, Peiyuan [2 ]
Guo, Ruilan [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
[2] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Beijing 100190, Peoples R China
基金
美国国家科学基金会;
关键词
Triptycene-containing copolyimides; Backbone rigidity; Gas separation membrane; FREE-VOLUME; SEPARATION MEMBRANES; POLYIMIDE MEMBRANES; PHILOSOPHICAL MAGAZINE; POROUS MATERIALS; POLYMERS; DIFFUSION; PERMEABILITY; HYDROCARBON; EDINBURGH;
D O I
10.1016/j.polymer.2017.04.016
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of triptycene-based copolyimides with varying backbone rigidity was synthesized and evaluated for chain packing behavior and gas transport properties. These copolymers were composed of a rigid element with the triptycene skeleton directly linked to imide rings and a relatively flexible element containing ether linkage and CF3 substituent groups. The ratio of the two components was systematically varied to investigate the effect of increasing triptycene density and steric hindrance while decreasing CF3 and ether linkage density. Generally, increasing the percentage of the directly-linked triptycene component increased chain rigidity, interchain spacing, and fractional free volume due to more highly disrupted chain packing. Therefore, copolymers with a high fraction of the directly-linked component showed increased gas permeabilities compared to the relatively flexible homopolymer counterpart. Additionally, the increase in triptycene density introduced more ultra-fine microcavities to facilitate in sieving, allowing for a concurrent maintenance or increase in selectivity. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:314 / 323
页数:10
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