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    Synthesis and characterization of 2′,3′-epoxy propyl-N-methyl-2-oxopyrrolidinium salicylate ionic liquid and study of its interaction with water or methanol
    (Royal Society of Chemistry, 2016) Vasanthakumar, Arumugam; Bahadur, Indra; Redhi, Gan G.; Gengan, Robert Moonsamy
    Important physico-chemical properties of ionic liquids (ILs) can be manipulated by adjusting the nature of the cation or anion. These properties are exploited in applications such as organic synthesis, catalysis and electrochemical processes to mention a few. In this work, the novel pyrrolidone ionic liquid N-(2′,3′-epoxypropyl)-N-methyl-2-oxopyrrolidinium salicylate [EPMpyr]+[SAL]− was synthesized using two steps and characterized. The temperature dependent density and speed of sound for ionic liquid, methanol, water, and their corresponding binary mixtures of {IL (1) + methanol or water (2)} were measured over the entire range of mole fractions at temperatures from T = (293.15 to 313.15) K in steps of 5 K, under atmospheric pressure. The calculated thermodynamic properties such as excess molar volume VEm, isentropic compressibility ks, intermolecular free length Lf, and deviation in isentropic compressibility Δks, were derived from the investigated density and speed of sound data. The resulting experimental data for excess molar volumes VEm, intermolecular free length Lf, and deviation in isentropic compressibility Δks, were well fitted to the Redlich–Kister polynomial equation. The effect of temperature and concentration on thermophysical properties was also provided.
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    Synthesis, characterization and thermophysical properties of ionic liquid N-methyl-N-(2′,3′-epoxypropyl)-2-oxopyrrolidinium chloride and its binary mixtures with water or ethanol at different temperatures
    (Elsevier, 2016) Vasanthakumar, Arumugam; Bahadur, Indra; Redhi, Gan G.; Gengan, Robert Moonsamy; Anand, Krishnan
    A novel ionic liquid, namely, N-methyl-N-(2′,3′-epoxypropyl)-2-oxopyrrolidiniumchloride [Epmpyr]+[Cl]− was synthesized and characterized by different techniques such as NMR (1H and 13C), FTIR, and elemental analysis. The water content of the ionic liquid was checked by Karl Fisher titration. Further, the density, ρ, and speed of sound, u, were measured for the above ionic liquid and the corresponding binary systems with water or ethanol at different temperatures ranging from (293.15 to 313.15) K. The derived thermodynamic properties for instance excess molar volumes, VE m isentropic compressibility, κs, and deviation in isentropic compressibility, Δκs, were investigated from the density and speed of sound data, respectively. It is noted that density and speed of sound of the ionic liquid and its binary mixtures were decreased with increase in temperature, whereas excess molar volume, isentropic compressibility, and deviation in isentropic compressibility values increased. Derived properties such as excess molar volumes, and deviation in isentropic compressibility data were fitted to the Redlich-Kister polynomial equation. The measured and calculated data were interpreted in terms of intermolecular interfaces and structural effects between similar and dissimilar molecules upon mixing.
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    Excess molar volumes of binary mixtures (an ionic liquid + water) : A review
    (Elsevier, 2015-03) Bahadur, Indra; Singh, Sangeeta; Redhi, Gan G.; Venkatesu, Pannuru; Letcher, Trevor M.
    This review covers recent developments in the area of excess molar volumes for mixtures of {ILs (1) + H2O (2)} where ILs refers to ionic liquids involving cations: imidazolium, pyridinium, pyrrolidinium, piperidinium, morpholinium and ammonium groups; and anions: tetraborate, triflate, hydrogensulphate, methylsulphate, ethylsulphate, thiocyanate, dicyanamide, octanate, acetate, nitrate, chloride, bromide, and iodine. The excess molar volumes of aqueous ILs were found to cover a wide range of values for the different ILs (ranging from −1.7 cm3 · mol−1 to 1.2 cm3 · mol−1). The excess molar volumes increased with increasing temperature for all systems studied in this review. The magnitude and in some cases the sign of the excess molar volumes for all the aqueous ILs mixtures, apart from the ammonium ILs, were very dependent on temperature. This was particularly important in the dilute IL concentration region. It was found that the sign and magnitude of the excess molar volumes of aqueous ILs (for ILs with hydrophobic cations), was more dependent on the nature of the anion than on the cation.
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    A rapid method for determining chlorobenzenes in dam water systems
    (Africa Journals Online, 2012-01-01) Moodley, Kandasamy G.; Chetty, Deenadayalan Kisten; Ramphal, Sayjil Rohith; Gericke, G.
    A method using direct immersion solid phase microextraction (DI-SPME) coupled to gas chromatography equipped with a flame ionisation detector (GC-FID) was developed for the analysis of 7 chlorinated benzenes in dam water. The main parameters affecting the DI-SPME process were optimised. The optimised method comprises the use of a 100 µm polydi-methylsiloxane (PDMS) fibre coating; 5 mℓ sample size; 700 r/min rate of agitation and an extraction time of 30 min. The calibration curve was linear with correlation coefficients ranging from 0.9957–0.9995 for a concentration range of 1–100 ng/mℓ. The limits of detection and quantification ranged from 0.020–0.265 ng/mℓ and 0.204–2.65 ng/mℓ, respectively. Recoveries ranged from 83.6–107.2% with relative standard deviation of less than 9.2%, indicating that the method has good precision. The method is reliable and is free of matrix interferences. Water samples collected from Grootdraai Dam were analysed using the optimised conditions to assess the potential of the method for trace level screening and quantification of chlorobenzenes. The method proved to be efficient, as 1,3 dichlorobenzene, 1,4-dichlorobenzene and pentachlorobenzene were detected at concentrations of 0.429 ng/mℓ, 1.685 ng/mℓ and 1.433 ng/mℓ, respectively.