4.6 Article

Effect of alkyl and aryl substitutions on 1,2,4-triazolium-based ionic liquids for carbon dioxide separation and capture

Journal

RSC ADVANCES
Volume 3, Issue 12, Pages 3981-3989

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ra22646d

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Funding

  1. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences, U. S. Department of Energy

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A series of 1,2,4-triazolium-based ionic liquids have been synthesized and evaluated for their use in supported ionic liquid membrane based CO2 separations. The properties of these triazolium-based compounds have proven sensitive to isomeric substitutions, such as isopropyl and propyl groups, as well as ortho and para substitutions in the aryl derivative compounds. While physical properties such as viscosity did not vary significantly between structural isomers, the CO2 permeability, selectivity, and solubility exhibited significant changes allowing for development of task-specific triazolium-based ionic liquids for separation applications. OSMOtherm studies were also completed to gain a better understanding of the ionic liquids which demonstrated a strong correlation between experimental and computational values for the alkyl bearing ionic liquids. Hence, 1,2,4-triazolium-based liquids comprise a class of compounds offering unique opportunities to examine how structural changes affect the physicochemical properties which are necessary for the continuous development of ionic liquids with enhanced adsorption capacity and selectivity in separations.

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