CO2 capture by polymeric membranes composed of hyper-branched polymers with dense poly(oxyethylene) comb and poly(amidoamine)

被引:4
|
作者
Taniguchi, Ikuo [1 ]
Wada, Norihisa [2 ]
Kinugasa, Kae [1 ]
Higa, Mitsuru [2 ]
机构
[1] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
[2] Yamaguchi Univ, Grad Sch Sci & Engn, 2-16-1 Tokiwadai, Ube, Yamaguchi 7558611, Japan
来源
OPEN PHYSICS | 2017年 / 15卷 / 01期
基金
日本科学技术振兴机构;
关键词
CO2; capture; gas permeability; macrophase separation; membrane separation; polymeric membrane; CO2-SELECTIVE MOLECULAR GATE; CARBON-DIOXIDE CAPTURE; POLY(ETHYLENE GLYCOL); GAS-TRANSPORT; SEPARATION; PERFORMANCE; DIFFUSION; PROGRESS;
D O I
10.1515/phys-2017-0077
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Due to CO2-philic nature of polyoxyethylene (POE), a dense POE comb structure was tethered onto PMMA backbone to develop CO2 separation membranes overN(2). The resulting hyper-branched polymers displayed preferential CO2 permeation. When the polymer thin layer was formed on a high gas permeable polydimethylsiloxane (PDMS) support by a spray-coating manner, the resulting thin film composite (TFC) membranes displayed very high CO2 permeability. However, the CO2 selectivity, which was the permeability ratio of CO2 over N-2, was moderate and lower than 50. To enhance the selectivity, poly(amidoamine) (PAMAM) was introduced to the hyper-branched polymers in the CO2-selective layer of the TFC membranes. The CO2 selectivity increased from 47 to 90 with increasing PAMAM content to 40 wt%, and it was drastically enhanced to 350 with PAMAM content of 50 wt%. Differential scanning calorimetry (DSC) and laser microscope revealed formation of PAMAM-rich domain at the higher amine content, whereCO(2) could readily migrate in comparison to the other polymeric fractions.
引用
收藏
页码:662 / 670
页数:9
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