کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
202767 | 460620 | 2012 | 6 صفحه PDF | دانلود رایگان |

The isobaric vapor–liquid equilibrium (VLE) data were determined, by using a recirculation type apparatus, for the binary mixtures of nonane with cyclohexane, toluene, m-xylene, or p-xylene at 101.3 kPa. All the data passed the thermodynamic consistency test and no azeotrope was formed in the investigated binary systems. While nonane + p-xylene were found to behave as near ideal systems, nonane + cyclohexane, nonane + toluene, and nonane + m-xylene exhibited large deviations from ideal behavior. The experimental results were used as a basis to check the validity of two predictive models, the UNIFAC and the conductor-like screening model for realistic solvents (COSMO-RS) models. These new VLE data were also correlated with the Wilson, the NRTL, and the UNIQUAC activity coefficient models.
► Isobaric binary vapor–liquid equilibrium (VLE) data were measured at 101.3 kPa.
► The studied systems are nonane with cyclohexane, toluene, m-xylene, or p-xylene.
► No azeotrope was formed and positive deviations from the Raoult's law were found.
► The UNIFAC and the COSMO-RS models were tested with the new VLE data.
► The Wilson, the NRTL, and the UNIQUAC models correlated well the VLE data.
Journal: Fluid Phase Equilibria - Volume 313, 15 January 2012, Pages 190–195