Interfacial properties of the ionic liquid [bmim][triflate] over a wide range of temperatures

• Published in: RSC advances 2018-01, Vol.8 (18), p.1115-1123
• Main Authors: Rivera, José L, Molina-Rodríguez, Luis, Ramos-Estrada, Mariana, Navarro-Santos, Pedro, Lima, Enrique
• Format: Article
• Language: English
• Subjects: Chains; Chemistry; Distribution functions; Equilibrium; Interfacial properties; Intermolecular forces; Ionic liquids; Liquid phases; Mathematical analysis; Molecular dynamics; Organic liquids; Radial distribution; Surface tension; Temperature
• ISSN: 2046-2069; 2046-2069
• DOI: 10.1039/c8ra00915e

We carried out molecular dynamics simulations of the liquid/vacuum equilibrium of the ionic liquid [bmim][triflate] in a wide range of temperatures (323.15 to 573.15 K). The results showed liquid phases with high densities even at temperatures close to the decomposition temperature of the liquid. The density and surface tension behaviors are linear across this wide range of temperatures, which is an extension of the behaviors of these systems at low temperatures, where these properties have been experimentally measured. The interfacial region shows peaks of adsorption of the ions; they are ordered, with the alkyl chains of the [bmim] cations pointing out of the liquid, and the tailing angle of the chains becomes 90° at higher temperatures. The alkyl chains are part of the outermost interfacial region, where intra- and intermolecular tangential forces are in equilibrium; thus, they do not contribute to the total surface tension. Unlike simpler organic liquids, the surface tension is composed of positive normal contributions of intermolecular interactions; these are almost in equilibrium with the negative normal contributions of intramolecular interactions, which are mainly vibrations of the distance and the angle of valence. The pressure profiles show that the molecules are in 'crushed' conformations internally in the bulk liquid and even more so in the normal direction at the interface. The total pressure profiles show values with physical meaning, where the tangential peaks show higher values than normal pressures and give rise to the surface tension. Short cutoff radii for the calculation of intermolecular forces (less than 16.5 Å) produce a system that is not mechanically stable in the region of the bulk liquid (confirmed by radial distribution function calculations); this produces a difference between the normal pressure and the average of the tangential pressures, which affects the calculation of the surface tension due to overestimation by up to 20% when using the global expression, which is extensively used for the calculation of surface tension. The use of a sufficiently long cutoff radius avoids these mechanical balance problems. Picture of the ionic liquid [bmim][triflate] at the vapor/vacuum interface. The liquid density and surface tension show linear behavior in a wide temperature range. The outer interfacial space shows a zero-surface tension zone.