Abstract
Three-component supercritical carbon dioxide-cosolvent (methanol, ethanol, water)-o-hydroxybenzoic acid (o-HBA) mixtures at a density of 0.7 g/cm3 and temperatures of 318 and 348 K are simulated by means of molecular dynamics. The solvate structures are investigated. It is shown that the solvation mechanism of o-HBA (particularly the o-HBA molecule forming a stable solvate complex with one molecule of a cosolvent via a hydrogen bond through the carboxyl group) does not depend on the temperature or the cosolvent. It is noted that the form of the cosolvent in a supercritical fluid varies: alcohols are distributed in the bulk in the form of monomers and hydrogen-bonded dimers, and water molecules tend to form microclusters along with chained and spatially branched structures by means of hydrogen bonds. It is established that the local molar fraction of cosolvent around the solvate complexes grows. It is concluded that the solvation of o-HBA is determined by the behavior of cosolvent in media of supercritical CO2.
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Original Russian Text © V.E. Petrenko, M.L. Antipova, D.L. Gurina, 2015, published in Zhurnal Fizicheskoi Khimii, 2015, Vol. 89, No. 3, pp. 414–419.
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Petrenko, V.E., Antipova, M.L. & Gurina, D.L. Structure of solvates of o-hydroxybenzoic acid in supercritical CO2-cosolvent media, according to molecular dynamics data. Russ. J. Phys. Chem. 89, 411–416 (2015). https://doi.org/10.1134/S0036024415030231
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DOI: https://doi.org/10.1134/S0036024415030231