TY - JOUR
T1 - An atomistic explanation of the ethanol-water azeotrope
AU - Carravetta, Vincenzo
AU - Gomes, Anderson Herbert de Abreu
AU - Marinho, Ricardo dos Reis Teixeira
AU - Öhrwall, Gunnar
AU - Ågren, Hans
AU - Björneholm, Olle
AU - de Brito, Arnaldo Naves
PY - 2022/10/14
Y1 - 2022/10/14
N2 - Ethanol and water form an azeotropic mixture at an ethanol molecular percentage of ∼91% (∼96% by volume), which prohibits ethanol from being further purified via distillation. Aqueous solutions at different concentrations in ethanol have been studied both experimentally and theoretically. We performed cylindrical micro-jet photoelectron spectroscopy, excited by synchrotron radiation, 70 eV above C1s ionization threshold, providing optimal atomic-scale surface-probing. Large model systems have been employed to simulate, by molecular dynamics, slabs of the aqueous solutions and obtain an atomistic description of both bulk and surface regions. We show how the azeotropic behaviour results from an unexpected concentration-dependence of the surface composition. While ethanol strongly dominates the surface and water is almost completely depleted from the surface for most mixing ratios, the different intermolecular bonding patterns of the two components cause water to penetrate to the surface region at high ethanol concentrations. The addition of surface water increases its relative vapour pressure, giving rise to the azeotropic behaviour.
AB - Ethanol and water form an azeotropic mixture at an ethanol molecular percentage of ∼91% (∼96% by volume), which prohibits ethanol from being further purified via distillation. Aqueous solutions at different concentrations in ethanol have been studied both experimentally and theoretically. We performed cylindrical micro-jet photoelectron spectroscopy, excited by synchrotron radiation, 70 eV above C1s ionization threshold, providing optimal atomic-scale surface-probing. Large model systems have been employed to simulate, by molecular dynamics, slabs of the aqueous solutions and obtain an atomistic description of both bulk and surface regions. We show how the azeotropic behaviour results from an unexpected concentration-dependence of the surface composition. While ethanol strongly dominates the surface and water is almost completely depleted from the surface for most mixing ratios, the different intermolecular bonding patterns of the two components cause water to penetrate to the surface region at high ethanol concentrations. The addition of surface water increases its relative vapour pressure, giving rise to the azeotropic behaviour.
U2 - 10.1039/d2cp03145k
DO - 10.1039/d2cp03145k
M3 - Article
C2 - 36268753
AN - SCOPUS:85140467634
VL - 24
SP - 26037
EP - 26045
JO - Physical chemistry chemical physics : PCCP
JF - Physical chemistry chemical physics : PCCP
SN - 1463-9084
IS - 42
ER -