Understanding temperature dependency of hydrogen solubility in ionic liquids, including experimental data in [bmim][Tf2N]

被引:36
作者
Raeissi, Sona [1 ]
Peters, Cor J. [2 ,3 ,4 ]
机构
[1] Shiraz Univ, Sch Chem & Petr Engn, Shiraz 71345, Iran
[2] Delft Univ Technol, Fac Mech Maritime & Mat Engn, Dept Proc & Energy, Lab Proc Equipment, NL-2628 CA Delft, Netherlands
[3] Petr Inst, Dept Chem Engn, Abu Dhabi, U Arab Emirates
[4] Eindhoven Univ Technol, Separat Technol Grp, Dept Chem Engn & Chem, NL-5600 MB Eindhoven, Netherlands
关键词
1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide; 1-butyl-3-methylimidazolium bis(trifluoromethylsullfonyl)amide; H2; phase equilibria; vapor-liquid equilibria; LOW-PRESSURE SOLUBILITIES; CARBON-DIOXIDE; PHASE-EQUILIBRIA; HYDROCARBON SYSTEMS; GASES; BEHAVIOR; H-2; TETRAFLUOROBORATE; THERMODYNAMICS; PREDICTION;
D O I
10.1002/aic.13742
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Previously unavailable high-pressure solubility data of hydrogen in 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide has been measured experimentally up to temperatures and pressures of 450 K and 15 MPa, respectively. In contrast to CO2 solubility, H2 tends to dissolve better in the ionic liquid at higher temperatures. This inverse temperature effect has been studied from a thermodynamic perspective and the underlying reason for this effect is explained. It is shown that the negative P-T slope is not limited to this particular binary mixture, but is the typical behavior in most, if not all, H2 + ionic liquid systems. However, there is a certain range of temperatures, pressures, and concentrations in which this phenomenon occurs. By predicting the Scott-van Konynenburg phase diagram for systems of H2 + ionic liquids to be of type III, it is shown how and why the solubility increases with temperature in some regions, but decreases in others. (c) 2012 American Institute of Chemical Engineers AIChE J, 2012
引用
收藏
页码:3553 / 3559
页数:7
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