Abstract

For over two decades, deep eutectic solvents have offered pre-eminence characteristics with the purpose of improving the issues of both ionic liquids and traditional solvents. The affordability, ease of preparation, in-flammability, non-or low toxicity, biodegradability, and other environmental advantages of DESs make them more appealing as green solvents. In the present study, 1-ethyl-1-methylpyrrolidinium bromide, a hydrogen bond accepter (HBA), was paired with 1,6-hexanediol (1,6-HDO), a hydrogen bond donor (HBD), to produce a DES with a mole ratio of 1:2. With the use of gas liquid chromatography (GLC), the infinite dilution activity coefficients (IDACs) of 32 different solutes were measured at different temperatures (313.15–343.15) K and atmospheric pressures. The partial molar properties, i.e., enthalpy, entropy, and Gibbs free energy, were calculated from the IDAC values at a reference temperature of T = 313.15 K to give more details for molecular interaction interpretation. Lastly, the selectivity and capacity values of separation problems such as benzene/acetone, benzene/cyclohexane, and cyclohexane/acetone were calculated from the IDAC values. The investigated DES was discovered to have good performance and could be used in industrial processes such as petroleum distillation, separation, extraction, and so on.

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