The effect of ionic liquid [Bmim][BF4] on the kinetics of CO2 desorption in amine solutions

被引:0
作者
Jia, Rui-Qi [1 ,2 ]
Xue, Zhi-Yuan [1 ,2 ]
Liang, Shuang [1 ,2 ]
Chu, Guang-Wen [1 ,2 ]
Zhang, Liang-Liang [1 ,2 ]
Chen, Jian-Feng [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, Res Ctr, Minist Educ High Grav Engn & Technol, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon capture; desorption; ionic liquid; organic amine; CARBON-DIOXIDE; ABSORPTION; SOLVENT; MECHANISM;
D O I
10.1002/aic.18780
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Here, the effect of ionic liquid (IL) on the kinetics of CO2 desorption in amine solutions was investigated. N-(2-aminoethyl) ethanolamine (AEEA) and N,N-diethylethanolamine (DEEA) were used as representatives of primary/secondary and tertiary amines. Results indicated that IL had a promoting effect on AEEA, but not on DEEA. The initial desorption rate of AEEA can be improved by up to 36.4%. Kinetics for IL-activated AEEA was developed through a modified Arrhenius equation, and the activation energy was 38.48 kJ/mol, which was 10.7% lower than that of AEEA. The species distribution was monitored by 13C NMR, which showed that the IL was not directly involved in the reaction, but might activate desorption through hydrogen bonding. Furthermore, theoretical calculations revealed that the IL can form hydrogen bonding with carbamate during the desorption of primary/secondary amines to lower the energy barrier for the zwitterion formation reaction, while only weaker hydrogen bonding was formed during the desorption of tertiary amines.
引用
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页数:10
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