Thermodynamics Research Center / ThermoML | Journal of Chemical Thermodynamics

Investigating the solubility of chlorophenols in hydrophobic ionic liquids

Sulaiman, R., Hadj-Kali, M.K., Hasan, S.W., Mulyono, S., AlNashef, I.M.
J. Chem. Thermodyn. 2019, 135, 97-106
ABSTRACT
Chlorophenols (CPs) are synthetic chemicals that are generated and used widely by different industries such as textile, pharmaceutical, metallurgic, oil, and pulp and paper manufacturing. Except water, most of the solvents used in these industries are volatile and toxic. Therefore, there is an imminent need for replacing these solvents by solvents that have less negative impact on the environment. In addition, CPs are considered as hazardous pollutants due to their resistance to biodegradation and persistence in the environment. Their toxic effects are severe including DNA damage, endocrine disruption, cytotoxicity, mutagenicity, and carcinogenicity. Hence, the water contaminated by CPs must be treated before being released to the environment. Ionic liquids (ILs) are molten salts that are liquid below 100 .deg.C, which have been used as solvents for many processes including liquid-liquid extraction and as electrolytes in electrochemical devices. ILs are characterized by negligible vapor pressure and non-flammability. These compounds are liquid over a wide range of temperatures; possess high thermal and chemical stability. ILs are being used as media for many reactions to reduce the negative impact of traditional solvents on the environment. In addition, using ILs as green solvents in water treatment has become a research hotspot. Solubility data of CPs in ILs is important for assessing the potential use of ILs as reaction media and in water treatment, but relevant data for ILs are scarce. To our best knowledge, no solubility data of chlorophenols in ILs were reported in the literature. Thus, in this study, the solubility of 3-chlorophenol (3-CP), 2,5-dichlorophenol (DCP), 2,4,6-trichlorophenol (TCP), and pentachlorophenol (PCP) in six hydrophobic bis(trifluoromethylsulfonyl)imide based ILs at 25 .deg.C, 35 .deg.C and 45 .deg.C was investigated. It was found that the solubility of 3-CP in all studied ILs at 25 .deg.C was greater than 70 wt%, thus the solubility measurements of 3-chlorophenol in the studied IL were stopped at 70 wt% and further measurement was not conducted. The solubility of other CPs in all studied ILs decreased with increasing the number of chlorine atoms in the CP and increased with the increase in temperature, but the degree of increase depended on the structure of both the IL and chlorinated phenol. In general, it was found that the tested chlorophenols have substantial solubility in pyridinium and imidazolium-based ILs. In addition, the non-random two-liquid model (NRTL) and Conductor-like Screening Model for Real Solvents (COSMO-RS) models were applied to predict the solubility of chlorophenols in all ILs used in this study. There was a good quantitative and qualitative agreement between experimental and calculated solubility data in most of the cases.
Compounds
# Formula Name
1 C6H5ClO 3-chlorophenol
2 C6H4Cl2O 2,5-dichlorophenol
3 C6H3Cl3O 2,4,6-trichlorophenol
4 C6HCl5O pentachlorophenol
5 C10H15F6N3O4S2 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide
6 C15H30F6N2O4S2 tributylmethylammonium bis((trifluoromethyl)sulfonyl)imide
7 C12H22F6N2O4S2 1-butyl-1-methylpiperidinium bis(trifluoromethanesulfonyl)imide
8 C7H13F6NO4S3 diethylmethylsulfonium bis[(trifluoromethyl)sulfonyl]imide
9 C12H16F6N2O4S2 1-butyl-3-methylpyridinium 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide
10 C10H12F6N2O4S2 1-ethyl-3-methylpyridinium bis((trifluoromethyl)sulfonyl)amide
11 H2O water
Datasets
The table above is generated from the ThermoML associated json file (link above). POMD and RXND refer to PureOrMixture and Reaction Datasets. The compound numbers are included in properties, variables, and phases, if specificied; the numbers refer to the table of compounds on the left.
Type Compound-# Property Variable Constraint Phase Method #Points
  • POMD
  • 2
  • 5
  • Mass fraction - 2 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 2
  • Chromatography
  • 3
  • POMD
  • 2
  • 6
  • Mass fraction - 2 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 2
  • Chromatography
  • 3
  • POMD
  • 2
  • 7
  • Mass fraction - 2 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 2
  • Chromatography
  • 3
  • POMD
  • 2
  • 8
  • Mass fraction - 2 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 2
  • Chromatography
  • 3
  • POMD
  • 2
  • 9
  • Mass fraction - 2 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 2
  • Chromatography
  • 3
  • POMD
  • 2
  • 10
  • Mass fraction - 2 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 2
  • Chromatography
  • 3
  • POMD
  • 3
  • 5
  • Mass fraction - 3 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 3
  • Chromatography
  • 3
  • POMD
  • 3
  • 6
  • Mass fraction - 3 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 3
  • Chromatography
  • 3
  • POMD
  • 3
  • 7
  • Mass fraction - 3 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 3
  • Chromatography
  • 3
  • POMD
  • 3
  • 8
  • Mass fraction - 3 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 3
  • Chromatography
  • 3
  • POMD
  • 3
  • 9
  • Mass fraction - 3 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 3
  • Chromatography
  • 3
  • POMD
  • 3
  • 10
  • Mass fraction - 3 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 3
  • Chromatography
  • 3
  • POMD
  • 4
  • 5
  • Mass fraction - 4 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 4
  • Chromatography
  • 4
  • POMD
  • 4
  • 6
  • Mass fraction - 4 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 4
  • Chromatography
  • 4
  • POMD
  • 4
  • 7
  • Mass fraction - 4 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 4
  • Chromatography
  • 4
  • POMD
  • 4
  • 8
  • Mass fraction - 4 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 4
  • Chromatography
  • 4
  • POMD
  • 4
  • 9
  • Mass fraction - 4 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 4
  • Chromatography
  • 4
  • POMD
  • 4
  • 10
  • Mass fraction - 4 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 4
  • Chromatography
  • 4
  • POMD
  • 1
  • 11
  • Mass concentration, kg/m3 - 1 ; Liquid mixture 1
  • Temperature, K; Liquid mixture 1
  • Pressure, kPa; Liquid mixture 1
  • Liquid mixture 1
  • Liquid mixture 2
  • Chromatography
  • 1