کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
230566 | 1427389 | 2014 | 8 صفحه PDF | دانلود رایگان |
• A complementary set of phase equilibrium data for CO2 + 1-pentanol and CO2 + 1-hexanol are presented.
• The saturation pressures were obtained using a variable-volume view cell.
• The experimental data were correlated using PR-vdW2, PR-WS and PSRK equations of state.
This work reports phase equilibrium measurements for the systems CO2(1) + 1-pentanol(2) and CO2(1) + 1-hexanol(2). Experiments were carried out using a high pressure variable-volume view cell with operating temperatures ranged from 303.15 K to 373.15 K and pressures up to 17.05 MPa for the system CO2 + 1-pentanol, and 303.15 K to 353.15 K with pressures up to 16.2 MPa for the system CO2 + 1-hexanol. The CO2 molar fractions were ranged from 0.3987 to 0.9192 for the system CO2(1) + 1-pentanol(2) and from 0.3926 to 0.9800 for the system CO2(1) + 1-hexanol(2), respectively. Only vapor–liquid (VL) phase transitions were observed for the system CO2(1) + 1-pentanol(2), while for the system with 1-hexanol(2) vapor–liquid (VL), liquid–liquid (LL) and vapor–liquid–liquid (VLL) phase transition were observed. The experimental data sets were modeled using the Peng–Robinson equation of state with a classical van der Waals quadratic mixing rule (PR-vdW2) and with Wong–Sandler (PR-WS) mixing rule, and they were compared with predicted values using the Predictive Soave–Redlich–Kwong (PSRK) equation of state. PR-WS model provided a better fitting to experimental data for both systems modeled.
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Journal: The Journal of Supercritical Fluids - Volume 88, April 2014, Pages 38–45