Molecular simulations of transport properties of polar hydrofluoroethers: Force field development, fractional Stokes-Einstein and free volume relations

0574386 - ÚT 2024 RIV NL eng J - Článek v odborném periodiku
Aminian, Ali - Vinš, Václav
Molecular simulations of transport properties of polar hydrofluoroethers: Force field development, fractional Stokes-Einstein and free volume relations.
Journal of Molecular Liquids. Roč. 389, November (2023), č. článku 122847. ISSN 0167-7322. E-ISSN 1873-3166
Grant CEP: GA ČR(CZ) GA22-03380S
Institucionální podpora: RVO:61388998
Klíčová slova: molecular dynamics simulations * transport properties * hydrofluoroether * free volume * stokes-einstein
Obor OECD: Thermodynamics
Impakt faktor: 6, rok: 2022
Způsob publikování: Omezený přístup
https://www.sciencedirect.com/science/article/pii/S0167732223016525?via%3Dihub

Hydrofluoroethers (HFEs) having simultaneously hydrocarbon (HC) and fluorocarbon (FC) moieties connected through ether oxygen are polar chain molecules with dielectric properties, which makes them a good heat transfer medium, e.g., for cooling of electronics or magnetic devices. In this work, we report, validate, and test high level-ab initio derived force fields and we use partial charges fitted to the electrostatic potential surface (EPS) to reproduce the dipole moments. Computer simulations were performed over a wide range of temperatures and densities to calculate the transport coefficients in the condensed-phase and comparisons were made against available experimental data for five selected molecules, namely HFE-7000, HFE-7100, HFE −7200, HFE −7300, and HFE −7500. Furthermore, structural properties and enthalpy of vaporization were obtained from molecular simulations. Cohen and Turnbull formula for the translational self-diffusion coefficient was tested in the free-volume cast, which itself was correlated against the isothermal compressibility, which can explain the phenomenon of transport properties in liquids, D∝exp-γ/Vf/V∗. The fractional Stokes-Einstein relation was also tested to scale the self-diffusion coefficient vs viscosity in the form of (DT−1) ∝ (1/η)s, with s ranging between ≈ 0.89 and 0.92 for the five molecules in the reduced density range of ρσ3 = 0.56 to 0.75. Finally, the non-equilibrium molecular dynamics (NEMD) simulations of thermal conductivity was found to outperform the equilibrium Green-Kubo approach, but both with comparable accuracy.
Trvalý link: https://hdl.handle.net/11104/0349188