TY - JOUR
T1 - CO2 capture by polymeric membranes composed of hyper-branched polymers with dense poly(oxyethylene) comb and poly(amidoamine)
AU - Taniguchi, Ikuo
AU - Wada, Norihisa
AU - Kinugasa, Kae
AU - Higa, Mitsuru
N1 - Funding Information:
Acknowledgement: The authors acknowledge Prof. Anne M. Mayes of Massachusetts Institute of Technology for invaluable support to develop the hyper-branched polymers. This research was partially supported by Grant-in-Aid for Scientific Research (C) Grant Number JP17899334 and the Advanced Carbon Technology Research and Development Program from Japan Science and Technology Agency. The International Institute for Carbon-Neutral Energy Research (WPI-I2CNER) is supported by the World Premier International Research Center Initiative (WPI), MEXT, Japan.
Publisher Copyright:
© 2017 Ikuo Taniguchi et al.
PY - 2017
Y1 - 2017
N2 - Due to CO2-philic nature of polyoxyethylene (POE), a dense POE comb structure was tethered onto PMMA backbone to develop CO2 separation membranes over N2. 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 N2, 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, where CO2 could readily migrate in comparison to the other polymeric fractions.
AB - Due to CO2-philic nature of polyoxyethylene (POE), a dense POE comb structure was tethered onto PMMA backbone to develop CO2 separation membranes over N2. 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 N2, 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, where CO2 could readily migrate in comparison to the other polymeric fractions.
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U2 - 10.1515/phys-2017-0077
DO - 10.1515/phys-2017-0077
M3 - Article
AN - SCOPUS:85035080581
SN - 1895-1082
VL - 15
SP - 662
EP - 670
JO - Open Physics
JF - Open Physics
IS - 1
ER -