Understanding Carbon Dioxide Solubility in Ionic Liquids by Exploring the Link with Liquid Clathrate Formation

被引:15
作者
Kelley, Steven P. [3 ]
Flores, Luis A. [1 ]
Shannon, Matthew S. [2 ]
Bara, Jason E. [2 ]
Rogers, Robin D. [1 ,4 ]
机构
[1] Univ Alabama, Dept Chem, Box 870336, Tuscaloosa, AL 35487 USA
[2] Univ Alabama, Dept Chem & Biol Engn, Box 870336, Tuscaloosa, AL 35487 USA
[3] McGill Univ, Dept Chem, 801 Sherbrooke St W, Montreal, PQ H3V 1B4, Canada
[4] 525 Solut Inc, 720 2nd St, Tuscaloosa, AL 35403 USA
基金
加拿大自然科学与工程研究理事会;
关键词
carbon dioxide capture; host-guest systems; ionic liquids; physisorption; supramolecular chemistry; PHASE-BEHAVIOR; CO2; CAPTURE; AROMATIC-COMPOUNDS; PHYSICAL SOLVENTS; GAS SOLUBILITY; PLUS; SEPARATIONS; SELECTIVITY; MIXTURES;
D O I
10.1002/chem.201703117
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The solubilities of the quadrupolar molecules benzene and CO2 in various ionic liquids (ILs) are compared in order to determine the connection between aromatic liquid clathrate formation and CO2 dissolution in ILs. It was found that both CO2 Henry's law constants and benzene solubility are remarkably well correlated with each other and with IL molar volume, suggesting both phenomena depend more on the strength of interionic interactions between the ions of an IL rather than the identity of either ion. However, IL ion-quadrupole interactions were found to have an effect for dicyanamide ([N(CN)(2)](-)), where solubility of CO2 and benzene are affected by destabilizing and stabilizing interactions with [N(CN)(2)](-), respectively. The results suggest both solubility phenomena are related to the incorporation of the solute into an IL host network. Aromatic liquid clathrate formation thus has potential as a facile experimental probe for predicting the relative ability of ILs to physisorb CO2.
引用
收藏
页码:14332 / 14337
页数:6
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