Published June 2019 | Version v1
Journal article

Physicochemical properties of choline chloride-based deep eutectic solvents and excess properties of their pseudo-binary mixtures with 1-butanol

  • 1. Departamento de Ingeniería Química y Bioprocesos, Pontificia Universidad Católica de Chile, Avenida Vicuña Mackenna 4860, Macul, Santiago (Chile)
  • 2. McKetta Department of Chemical Engineering, University of Texas at Austin, Austin, TX 78712 (United States)
  • 3. Departamento de Química Física, Facultad de Química y de Farmacia, Pontificia Universidad Católica de Chile, Avenida Vicuña Mackenna 4860, Macul, Santiago (Chile)

Description

Highlights: • Deep eutectic solvents based on choline chloride were characterized with NMR, FT-IR, TGA and surface tension. • Densities and viscosities were measured for deep eutectic solvents and their pseudo-binary mixtures with 1-butanol. • Enthalpies of mixing were obtained for pseudo-binary mixtures of deep eutectic solvent + 1-butanol. -- Abstract: Ionic liquids and deep eutectic solvents have aroused interest as alternative solvents for separation processes due to their favourable properties. For instance, deep eutectic solvents are usually biodegradable, non-toxic, low cost and also share some properties with ionic liquids, such as their tuneability to be used in specific applications. Recently, deep eutectic solvents have been studied more extensively but their physicochemical characterization is still in the initial stages if the final objective is to select alternatives for industrial processes. Decomposition temperature, surface tension, density, and viscosity were measured for deep eutectic solvents based on choline chloride as the hydrogen bond acceptor and levulinic acid, ethylene glycol and phenol as hydrogen bond donors (in a 1:2 mol ratio). Density, viscosity and excess enthalpy were measured for pseudo-binary mixtures of the different deep eutectic solvents with 1-butanol. The excess properties were calculated to understand the behaviour of the deep eutectic solvents in the mixture. The results suggest that deep eutectic solvents are formed due to strong intermolecular forces between their constituents, with no reaction observed. This generates a higher thermal stability of the deep eutectic solvents compared to their constituent hydrogen bond donor. Also, with the addition of 1-butanol to the deep eutectic solvents, the mixture has a lower volume compared with the ideal case due to the creation of new networks of hydrogen bonds and interstitial site accommodations. Hence, the excess molar volumes and excess enthalpies have a negative deviation from the ideal behaviour. The viscosity deviation is related to the Arrhenius equation observing a negative deviation for the deep eutectic solvents containing levulinic acid and phenol, and a positive deviation for the one with ethylene glycol. Experimental data for the different properties allows a qualitative understanding of the magnitude of the interactions that occur when mixing deep eutectic solvents with 1-butanol.

Additional details

Identifiers

DOI
10.1016/j.jct.2019.02.010;
PII
S0021961418309996;

Publishing Information

Journal Title
Journal of Chemical Thermodynamics
Journal Volume
133
Journal Page Range
p. 272-284
ISSN
0021-9614
CODEN
JCTDAF

Optional Information

Copyright
Copyright (c) 2019 Elsevier Ltd.