Gas sorption and transport in thermally rearranged polybenzoxazole membranes derived from polyhydroxylamides

被引:40
|
作者
Kim, Seungju [1 ]
Seong, Jong Geun [1 ]
Do, Yu Seong [1 ]
Lee, Young Moo [1 ]
机构
[1] Hanyang Univ, Coll Engn, Dept Energy Engn, Seoul 133791, South Korea
基金
新加坡国家研究基金会;
关键词
Thermally rearranged polymers; Gas sorption; Solubility coefficient; Dual-mode sorption; Polybenzoxazole; INTRINSIC MICROPOROSITY; POLYMER MEMBRANES; GLASSY-POLYMERS; CARBON-DIOXIDE; TROGERS BASE; SEPARATION; PERMEATION; DIFFUSION;
D O I
10.1016/j.memsci.2014.09.051
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The sub-nano-sized microcavities in microporous thermally rearranged (TR) polymers can be tuned by varying the conditions of thermal rearrangement. Relatively small cavities were formed by thermal rearrangement of poly(o-hydroxylamide) (PHA) precursors compared to the cavities formed by that of polyimide precursors. TR polymers derived from PHAs, so-called TR-beta-polymers, are known to exhibit a well-tuned cavity structure that can be used for H-2/CO2 separation. According to a solution-diffusion model, both the permeability and selectivity for H-2/CO2 separation were improved at elevated temperatures due to a significant increase in H-2 diffusion and a decrease in CO2 sorption. In this study, gas solubility and permeability of five representative small gas molecules (H-2, N-2, O-2, CH4, and CO2) through TR-beta-polymer membranes were characterized between 20 degrees C and 65 degrees C for gas solubility measurement and between 35 degrees C and 300 degrees C for gas permeability measurement. These measurements allowed for the calculation of thermodynamic factors such as the activation energy and heat of sorption. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:122 / 131
页数:10
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