Exploring the dynamic world of ternary deep eutectic solvents: Synthesis, characterization, and key properties unveiled

Abstract

Deep eutectic solvents are a novel class of solvents that have gained much attention with time due to their biodegradability, non-volatility, non-toxicity and low-cost. In this work, a novel ternary deep eutectic solvent (TDES) was synthesized using ethaline (ChCl:EG) and glycine, with the addition of carboxylic acids. The synthesized material was characterized through Fourier-transform infrared spectroscopy (FTIR). While the thermal stability and physical properties such as density, viscosity, surface tension and refractive index were also determined). To estimate the critical properties, modified version of Lyderson-Joback-Reid (LJR) and Lee-Kesler mixing (Alkhatib et al., 2020) [1] methods were used. The density of the DES was calculated using the Spencer and Danner correlation and the obtained values were compared with experimental data. FTIR analysis confirmed that hydrogen bonding is the main driving force responsible for the formation of the deep eutectic solvents. The physical properties of the binary DES system, such as viscosity, density,and thermal stability of the system were enhanced after the incorporation of a third component (carboxylic acid) to the system. However, the surface tension of the TDES system decrease with the increasing amounts of the third component, likely due to increase in the void radius of the TDES. Thus investigation is considering as novel work to check the influence of carboxylic acids on the physical properties of binary deep eutectic solvent systems.