Solubility Measurement and Data Correlation of Cyclohexanone, tert-Butanol, and 1,4-Dioxane in p-, o-, and m-Xylenes and Ethylbenzene

The solubility of cyclohexanone, tert-butanol,and 1,4-dioxane in p-, o-, and m-xylenes and ethylbenzene was measured by a gas chromatographymethod under an atmospheric environment. The measured data indicatedthat the solubility of cyclohexanone, tert-butanol,and 1,4-dioxane in the xylenes and ethylbenzene increases with increasingtemperature. The experimentally determined solubility results werefitted with the modified Apelblat equation, Van't Hoff equation,and Wilson model. Among them, the Wilson model was most consistentwith the measured solubility results. The dissolution-related thermodynamicproperties of cyclohexanone, tert-butanol, and 1,4-dioxanein xylenes and ethylbenzene, including the changes of molar Gibbsfree energy, molar enthalpy, and molar entropy, were predicted andanalyzed via the correlated Wilson model, which indicates that thedissolution behaviors are spontaneous and endothermic process. Theobtained solubility results provide the thermodynamic foundation forthe development and upgrading of industrial separation processes relatedto xylene, ethylbenzene, cyclohexanone, tert-butanol,and 1,4-dioxane.

Automated summary

The solubility of cyclohexanone, tert-butanol, and 1,4-dioxane in various xylenes and ethylbenzene was measured, and it was found that the solubility increased with temperature. The Wilson model was the most accurate in fitting the solubility results. Furthermore, the dissolution behaviors of the compounds were analyzed using the Wilson model, and it was determined that the process is spontaneous and endothermic. The obtained solubility results have implications for the development and improvement of industrial separation processes involving these compounds.