[1] Cadena, C., Anthony, J. L., Shah, J. K., Marrow, T. I., Brennecke, J. F. and Maggin, E. J., “Why is CO2 so soluble in imidazolium-based ionic liquids?”, J. Am. Chem. Soc., 126, 5300 (2004).
[2] Bara, J. E., Carlisle, T. K., Gabriel, C. J., Camper, D., Gin, D. L. and Noble, R. D., “Guide to CO2 separations in imidazolium-based room temperature ionic liquids”, Ind. Eng. Chem. Res., 48, 2739 (2009).
[3] Keskin, S., Kayrak-Talay, D., Akman, U. and Hortacsu, O. “A review of ionic liquids towards supercritical fluid applications”, J. Supercrit. Fluids, 43, 150 (2007).
[4] Shokouhi, M., Adibi, M., Jalili, A. H., Hosseini-Jenab, M. and Mehdizadeh, A., “Solubility and Diffusion of H2S and CO2 in the Ionic Liquid 1-(2-Hydroxyethyl)-3- methylimidazolium Tetrafluoroborate”, J. Chem. Eng. Data., 55, 1663 (2010).
[5] Jalili, A. H., Mehdizadeh, A., Shokouhi, M., Sakhaeinia H. and Taghikhani, V., “Solubility of CO2 in 1-(2-hydroxyethyl)-3-methylimidazolium ionic liquids with different anions”, J. Chem. Thermodyn., 42, 787 (2010).
[6] Camper, D., Bara, J. E., Gin, D. L. and Noble, R. D., “Room-temperature ionic liquidamine solutions: Tunable solvents for efficient and reversible capture of CO2”, Ind. Eng. Chem. Res., 47, 8496 (2008).
[7] Cole, A. C., Jensen, J. L., Nta, I., Tran, K. L. T., Weaver, K. J., Forbes, D. C. and Davis, “Novel Brønsted acidic ionic liquids and their use as dual solvent-catalysts”, J. H., J. Am. Chem. Soc., 124, 5962 (2002).
[8] Gutowski, K. E. and Maginn, “Amine-functionalized task-specific ionic liquids: a mechanistic explanation for the dramatic increase in viscosity upon complexation with CO2 from molecular simulation”, J. Am. Chem. Soc. 130, 14690 (2008).
[9] Bates, E. D., Mayton, R. D., Ntai, I., Davis, J. H., “CO2 capture by a task-specific ionic liquid”, J. Am. Chem. Soc., 124, 926 (2002).
[10] Karadas, F., Atilhan, M. and Aparicio, S., “Review on the Use of Ionic Liquids (ILs) as Alternative Fluids for CO2 Capture and Natural Gas Sweetening”, Energy & Fuels, 24, 5817 (2010).
[11] Ahmady, A., Hashim, M. A. and Aroua, M. K., “Experimental investigation on the solubility and initial rate of absorption of CO2 in aqueous mixtures of methyldiethanolamine with the ionic liquid 1-Butyl-3-methylimidazolium Tetrafluoroborate”, J. Chem. Eng. Data., 55, 5733 (2010).
[12] Shojaeian, A. and Haghtalab, A., “Solubility and density of carbon dioxide in different aqueous alkanolamine solutions blended with 1-butyl-3 methylimidazolium acetate ionic liquid at high pressure”, J. Mol. Liq., 187, 218 (2013).
[13] Chinn, D., Vu, D. Q., Driver, M. S. and Boudreau, L. C., “CO2 removal from gas using ionic liquid absorbents”, U.S. Pat. 20060251558, Nov 9, (2006).
[14] Zhang, F., Fang, C. G., Wu, Y. T., Wang, Y. T., Li, A. M. and Zhang, Z. B., “
Absorption of CO2 in the aqueous solutions of functionalized ionic liquids and MDEA”,
Chem. Eng. J.,
160, 691 (2010).
[15] Zhang, F., Ma, J. W., Zhou, Z., Wu, Y. T. and Zhang, Z. B., “
Study on the absorption of carbon dioxide in high concentrated MDEA and ILs solutions”,
Chem. Eng. J.,
181, 222 (2012).
[19] Sairi, N. A., Yusoff, R., Alias, Y. and Aroua, M. K., “Solubilities of CO2 in aqueous N-methyldiethanolamine and guanidinium trifluoromethanesulfonate ionic liquid systems at elevated pressures”, Fluid. Phase. Equilib., 300, 89 (2011).
[20] Holbrey, J. D., Reichert, W. M., Swatloski, R. P., Broker, G. A., Pitner, W. R., Seddon, K. R. and Rogers R. D., “Efficient, halide-free synthesis of new, low cost ionic liquids: 1,3 dialkylimidozolium salts containing methyl- and ethylsulfate anions”, Green Chem., 4, 407 (2002).
[21] Jalili, A. H., Mehdizadeh, A., Shokouhi, M., Ahmadi A. N. Hosseini-Jenab, M. and Fateminassab, F., “Solubility and diffusion of CO2 and H2S in the ionic liquid 1-ethyl-3- methylimidazolium ethylsulfate”, J. Chem. Thermodyn., 42, 1298 (2010).
[22] Peng, Y. and Song, G., “Amino-Functionalized Ionic Liquid as a Catalytically Active Solvent for Microwave-Assisted Synthesis of 4H-Pyrans”, Cat. Commun., 8, 111 (2007).
[23] Jalili, A. H., Rahmati-Rostami, M., Ghotbi, C., Hosseini-Jenab, M. and Ahmadi, A. N., “Solubility of H2S in Ionic Liquids [bmim][PF6], [bmim][BF4], and [bmim][Tf2N]”, J. Chem. Eng. Data., 54, 1844 (2009).
[24] Shokouhi, M., Farahani, H. and Hosseini-Jenab, M., “Experimental solubility of hydrogen sulfide and carbon dioxide in Dimethylformamide and Dimethylsulfoxide”, Fluid. Phase. Equilib., 367, 29 (2014).
[25] Mazloumi, H., Haghtalb, A., Jalili, A. H. and Shokouhi, M. “Solubility of H2S in aqueous diisopropanolamine +piperazine solutions: new experimental data and modeling with the electrolyte Cubic Square-Well Equation of State”, J. Chem. Eng. Data. 57, 2625 (2012).
[26] Jalili, A. H., Shokouhi, M., Maurer, G. and Hosseini-Jenab, M., “Solubility of CO2 and H2S in the ionic liquid 1-ethyl-3-methylimidazolium tris(pentafluoroethyl) trifluorophosphate”, J. Chem. Thermodyn., 67, 55 (2013).
[27] Shokouhi, M., Farahani, H., Hosseini-Jenab, M. and Jalili, A. H., “
Solubility of Hydrogen Sulfide in N-Methylacetamide and N,NDimethylacetamide: Experimental Measurement and Modeling”,
J. Chem. Eng. Data.,
60, 499 (2015).
[28] NIST chemistry web book http://webbook. nist.gov/chemistry/fluid/ (accessed May 2010)
[29] Park, M. K. and Sandall, O. C., “Solubility of Carbon Dioxide and Nitrous Oxide in 50 mass % Methyldiethanolamine”, J. Chem. Eng. Data., 46, 166 (2001).
[30] Hosseini-Jenab, M., Abedinzadegan, M., Najibi, S. H., Vahidi, M. and Matin, N. S., “Solubility of Carbon Dioxide in Aqueous Mixtures of N-Methyldiethanolamine + Piperazine + Sulfolane”, J. Chem. Eng. Data., 50, 583 (2005).
[31] Jou, F. Y., Mather, A. E. and Otto, F. D., “Solubility of H2S and CO2 in Aqueous Methyldiethanolamine Solutions”, Ind. Eng. Chem. Process Des., 21, 539 (1982).
[32] MacGregor, R. J. and Mather, A. E., “Equilibrium Solubility of H2S and CO2 and Their Mixtures in a Mixed Solvent”, Can. J. Chem. Eng., 69, 1357 (1991).
[33] Brunner, E., Hueltenschmidt, W. and Schlichthaerle, G., “Fluid mixtures at high pressures IV. Isothermal phase equilibria in binary mixtures consisting of (methanol + hydrogen or nitrogen or methane or carbon monoxide or carbon dioxide)”, J. Chem. Thermodyn., 19, 273 (1987).