Reversible Capture of SO2 through Functionalized Ionic Liquids

被引:144
作者
Yang, Dezhong [1 ]
Hou, Minqiang [1 ]
Ning, Hui [1 ]
Ma, Jun [1 ]
Kang, Xinchen [1 ]
Zhang, Jianling [1 ]
Han, Buxing [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Key Lab Colloid & Interface & Thermodynam, Beijing Natl Lab Mol Sci, Beijing 10080, Peoples R China
基金
中国国家自然科学基金;
关键词
absorption; green chemistry; ionic liquids; reversibility; sulfur dioxide; FLUE-GAS DESULFURIZATION; HIGHLY EFFICIENT SO2; SULFUR-DIOXIDE; DRY-DESULFURIZATION; CO2; ABSORPTION; SOLUBILITY; MIXTURE;
D O I
10.1002/cssc.201300224
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Emission of SO2 in flue gas from the combustion of fossil fuels leads to severe environmental problems. Exploration of green and efficient methods to capture SO2 is an interesting topic, especially at lower SO2 partial pressures. In this work, ionic liquids (ILs) 1-(2-diethylaminoethyl)-3-methylimidazolium bis( trifluoromethylsulfonyl)imide ([Et(2)NEMim][Tf2N]) and 1-(2-di-ethylaminoethyl)- 3-methylimidazolium tetrazolate ([Et2NEMim][ Tetz]) were synthesized. The performances of the two ILs to capture SO2 were studied under different conditions. It was demonstrated that the ILs were very efficient for SO2 absorption. The [Et(2)NEMim][Tetz] IL designed in this work could absorb 0.47 g(SO2) g(IL)(-1) at 0.0101 MPa SO2 partial pressure, which is the highest capacity reported to date under the same conditions. The main reason for the large capacity was that both the cation and the anion could capture SO2 chemically. In addition, the IL could easily be regenerated, and the very high absorption capacity and rapid absorption/desorption rates were not changed over five repeated cycles.
引用
收藏
页码:1191 / 1195
页数:5
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