Solubility of CO2 in dialkylimidazolium dialkylphosphate ionic liquids

Authors
Palgunadi, JelliarkoKang, Je EunNguyen, Dinh QuanKim, Jin HyungMin, Byoung KounLee, Sang DeukKim, HonggonKim, Hoon Sik
Issue Date
2009-10-10
Publisher
ELSEVIER SCIENCE BV
Citation
THERMOCHIMICA ACTA, v.494, no.1-2, pp.94 - 98
Abstract
The solubility of carbon dioxide in room temperature ionic liquids (RTILs), dialkylimidazolium dialkylphosphates, was measured at 313-333 K and at pressures close to atmospheric pressure, from which Henry's law coefficients, standard Gibbs free energy, enthalpy, and entropy changes of solvation were derived. The CO2 solubility in the dialkylimidazolium dialkyl phosphate was found to increase with increasing chain length of the alkyl groups on the cation and/or the anion as was similarly found in other RTILs. Among various dialkylimidazolium dialkylphosphates tested, 1-ethyl-3-methylimidazolium diethylphosphate ([EMIM][Et2PO4]) and 1-butyl-3-methylimidazolium dibutyl phosphate ([BMIM][Bu2PO4]) exhibited the comparable or better capability of dissolving CO2 in comparison with that of [BMIM][BF4], but their absorption capacities were still lower than that of 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide([BMIM][Tf2N]). (C) 2009 Elsevier B.V. All rights reserved.
Keywords
PRESSURE PHASE-BEHAVIOR; CARBON-DIOXIDE; IMIDAZOLIUM; TETRAFLUOROBORATE; MIXTURES; HYDROGEN; SYSTEMS; CATION; ANION; PRESSURE PHASE-BEHAVIOR; CARBON-DIOXIDE; IMIDAZOLIUM; TETRAFLUOROBORATE; MIXTURES; HYDROGEN; SYSTEMS; CATION; ANION; CO2 capture; Ionic liquids; Dialkylimidazolium dialkylphosphate
ISSN
0040-6031
URI
https://pubs.kist.re.kr/handle/201004/132036
DOI
10.1016/j.tca.2009.04.022
Appears in Collections:
KIST Article > 2009
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