Measurement and correlation of solubility and thermodynamic properties of dicumyl peroxide (DCP) in pure and binary solvents

The solid-liquid equilibrium data of dicumyl peroxide (DCP) in seven pure solvents and ethanol-water binary system and DMF-water binary system were measured from 274.15 K to 302.15 K by a gravimetric method under atmospheric pressure. The results show that the solid-liquid equilibrium solubility of...

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Veröffentlicht in:Journal of molecular liquids 2020-09, Vol.314, p.113268, Article 113268
Hauptverfasser: Zhou, Jing, Hao, Lin, Hao, Hongxun, Yu, Zengrui, Zhou, Lina
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Sprache:eng
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Zusammenfassung:The solid-liquid equilibrium data of dicumyl peroxide (DCP) in seven pure solvents and ethanol-water binary system and DMF-water binary system were measured from 274.15 K to 302.15 K by a gravimetric method under atmospheric pressure. The results show that the solid-liquid equilibrium solubility of DCP rapid increased with augmented temperature in different types of pure solvent while the solubility in binary solvent mixtures increases with the increasing of the fraction of ethanol and DMF. The measured data in pure solvents were correlated with several thermodynamic models including the modified Apelblat model, λh model and NRTL model. All the experimental results were agreement with the fitted values. Moreover, the NRTL model was adopted to calculate the enthalpy, entropy and Gibbs energy change during the dissolution process. And for the binary solvent system, the CNIBS/R-K model was used to correlate the solubility data. It was found that the correlated results by the NRTL model agreed best with the experimental data. Besides the results indicate that the mixing process of dicumyl peroxide in the experimental solvents was spontaneous and entropy-driven. •The DCP solubility was maximal in pure DMF and minimal in pure methanol.•Thermodynamic quantities of solution and mixing were obtained for DCP.•The effect of solvent compositions on the solubility data were evaluated and discussed.
ISSN:0167-7322
1873-3166
DOI:10.1016/j.molliq.2020.113268