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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.
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页码:122 / 131
页数:10
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