resumo
Despite some promising potential applications of eutectic systems containing choline chloride ([Ch]Cl) and a polyalcohol, a detailed investigation of the thermodynamic behavior of these systems is still missing. In this work, the solid-liquid equilibria phase diagrams of binary systems containing [Ch]Cl and one from six different polyalcohols (ethylene glycol (EG), 1,3-propanediol, glycerol (Gly), meso-erythritol, xylitol, and sorbitol) were measured in the full composition. Except for the mixtures with Gly or EG, a quasi-ideal behavior in the [Ch]Cl solubility curve is observed. In the polyalcohol solubility curve, the mixtures present small negative deviations from ideality, except for [Ch]Cl + EG, which is slightly positive. The solid-liquid phase diagrams show a large liquid composition window, and not a fixed stoichiometry for the eutectic points, where the mixtures can be used as solvents close to, or below, room temperature. Aiming at their application, viscosities and densities were measured at the eutectic point in the temperature range from 278.15 to 373.15 K. All systems present densities and viscosities higher than water, which is directly related to the strong interactions between the components. Solvatochromic parameters were measured to characterize the solvents, and they show that solvent tunability can be achieved by varying the polyalcohol mole fraction.
palavras-chave
PHASE-CHANGE MATERIALS; CHOLINE CHLORIDE; SOLVATOCHROMIC PARAMETERS; THERMODYNAMIC PROPERTIES; AQUEOUS MIXTURES; THERMAL-BEHAVIOR; ETHYLENE-GLYCOL; GLYCEROL; GREEN; TEMPERATURE
categoria
Chemistry; Science & Technology - Other Topics; Engineering
autores
Silva, LP; Martins, MAR; Conceicao, JHF; Pinho, SP; Coutinho, JAP
nossos autores
Liliana Patrocínio da Silva
Colaborador
agradecimentos
This work was developed within the scope of the project CICECO-Aveiro Institute of Materials, UIDB/50011/2020 & UIDP/50011/2020, and CIMO-Mountain Research Center, UIDB/00690/2020, both financed by national funds through the Portuguese Foundation for Science and Technology/MCTES. The NMR spectrometers are part of the National NMR Network (PTNMR) and are partially supported by Infrastructure Project No 022161 (cofinanced by FEDER through COMPETE 2020, POCI and PORL and FCT through PIDDAC). L.P.S. acknowledges FCT for her PhD grant (SFRH/BD/135976/2018).