Search from over 60,000 research works

Advanced Search

Vaporisation and thermal decomposition of dialkylimidazolium halide ion ionic liquids

Full text not archived in this repository.
Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email

Lovelock, K. R. J. orcid id iconORCID: https://orcid.org/0000-0003-1431-269X, Armstrong, J. P., Licence, P. and Jones, R. G. (2014) Vaporisation and thermal decomposition of dialkylimidazolium halide ion ionic liquids. Physical Chemistry Chemical Physics, 16 (4). pp. 1339-1353. ISSN 1463-9076 doi: 10.1039/c3cp52950a

Abstract/Summary

Vaporisation and liquid phase thermal decomposition, TD, of two halide ion ionic liquids, 1-octyl-3-methylimidazolium chloride, [C8C1Im]Cl, and 1-octyl-3-methylimidazolium iodide, [C8C1Im]I, are investigated using temperature programmed desorption (TPD) line of sight mass spectrometry (LOSMS) at ultra-high vacuum (UHV). The ability to use MS to distinguish between vaporisation and TD allows the thermodynamics/kinetics of both vaporisation and TD to be investigated within the same experiments. Vaporisation of both halide ion ionic liquids is demonstrated. For both [C8C1Im]Cl and [C8C1Im]I the vapour is shown to be composed of neutral ion pairs (NIPs). The enthalpy of vaporisation at temperature T, ΔvapHT, was experimentally determined as ΔvapH455 = 151 ± 10 kJ mol−1 for [C8C1Im]Cl and ΔvapH480 = 149 ± 8 kJ mol−1 for [C8C1Im]I. Extrapolation of ΔvapHT to the reference temperature, 298 K, gave ΔvapH298 = 166 ± 10 kJ mol−1 for [C8C1Im]Cl and ΔvapH298 = 167 ± 8 kJ mol−1 for [C8C1Im]I, higher than most ΔvapH298 values measured to date for other [C8C1Im]+-containing ionic liquids. In addition, predictions of ΔvapH298 for other halide ion ionic liquids are made. Liquid phase TD is shown to proceed via nucleophilic substitution to give two sets of products: 1-octylimidazole and methylhalide, and 1-methylimidazole and 1-octylhalide. The activation energy of TD at a temperature T, Ea,TD,T, is measured for the nucleophilic substitution of [C8C1Im]I to give methyliodide; Ea,TD,480 = 136 ± 15 kJ mol−1. Ea,TD,T is measured for the nucleophilic substitution of [C8C1Im]Cl to give methylchloride; Ea,TD,455 = 132 ± 10 kJ mol−1. The fact that ΔvapHT and Ea,TD,T are the same (within error) for both ionic liquids is commented upon, and conclusions are drawn as to the thermal stability of these ionic liquids.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/76259
Item Type Article
Refereed Yes
Divisions Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
Publisher Royal Society of Chemistry
Download/View statistics View download statistics for this item

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar