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A computational strategy based on molecular dynamics (MD) simulations is proposed for the 14 prediction of tracer diffusion coefficients of bioactive compounds in CO2 ( ) and CO 𝐷12 2 modified 15 with ethanol ( ), in both supercritical and subcritical regions. Three systems were used for its 𝐷m,i 16 validation, namely, β-carotene and ibuprofen in supercritical CO2, and gallic acid in CO2 modified 17 with 16 mol.% of ethanol. The MD diffusivities were assessed with experimental data, with 18 average absolute relative deviations (AARD) between 3.82 % and 7.36 %, and average relative 19 deviations (ARD) between -6.18 % and 5.75 %. The dependency of the diffusion coefficient on 20 temperature, pressure, and Stoke-Einstein coordinate ( ) was also evaluated. All data followed 𝑇 𝜇 21 the expected trends apart from gallic acid in CO2 modified with 16 mol.% of ethanol, for which 22 the computed showed a weak linear dependency with . 𝐷m,i 𝑇 𝜇 23 The validated MD strategy was then employed to calculate diffusivities of eucalyptol in 24 sub/supercritical CO2, and in sub/supercritical CO2 modified with 8 mol.% and 16 mol.% of 25 ethanol. The computational strategy was re-evaluated upon comparison with experimental 26 diffusivities of eucalyptol in sub/supercritical mixtures of CO2 with 8 mol.% ethanol. The 27 expected dependencies on pressure, temperature, and Stoke-Einstein coordinate were obeyed, and 28 it was also found that the diffusion coefficient decreased with increasing ethanol content. Four 29 phenomenological models from the literature were adopted to represent MD data, with AARD 30 values between 1.21 % and 4.40 %, suggesting they can be used for diffusivity estimations over 31 wider ranges of operating conditions. published |
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