Dissemin is shutting down on January 1st, 2025

Published in

American Chemical Society, Journal of Chemical and Engineering Data, 10(55), p. 4514-4520, 2010

DOI: 10.1021/je100377k

Links

Tools

Export citation

Search in Google Scholar

Structural and Positional Isomerism Influence in the Physical Properties of Pyridinium NTf2-Based Ionic Liquids: Pure and Water-Saturated Mixtures†

This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
  • Must obtain written permission from Editor
  • Must not violate ACS ethical Guidelines
Orange circle
Postprint: archiving restricted
  • Must obtain written permission from Editor
  • Must not violate ACS ethical Guidelines
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

Density and viscosity data for six pyridinium-based ionic liquids combined with the bis[(trifluoromethyl)-sulfonyl]amide anion were measured at atmospheric pressure in the (278 to 363) K temperature range. The fundamental aim of this work is to study the effect of the structure of the pyridinium-based cation, namely, its alkyl chain length and structural isomers, and the position of the second alkyl substitution on the measured properties. Albeit many studies exist on the physical properties of ionic liquids in what concerns the nature of the anion and the length of the cation alkyl side chain, the effect of structural and positional isomerism on those properties is much less known. In additionsand since small amounts of water influence the phase equilibrium and thermophysical properties of ionic liquidsswater-saturated ionic liquid samples were also studied in the (298 to 363) K temperature range. The Vogel-Tammann-Fulcher (VTF) method was applied to describe the viscosity data, and novel group contribution parameters are proposed for the ionic liquid cations presented here, thus broadening its applicability.