High-pressure vapor–liquid equilibria of methanol+propylene: Experimental and modeling with SAFT

• Published in: The Journal of supercritical fluids Vol. 63; pp. 25 - 30
• Main Authors: Banaei, M., Florusse, L.J., Raeissi, S., Peters, C.J.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.03.2012
• Subjects: Computational fluid dynamics; Correlation; Deviation; Fluid flow; Fluids; Methanol; Methyl alcohol; Phase behavior; Propene; Propylene; Raoult law; Statistical associating fluid theory equation of state; Propylene; Propene; Statistical associating fluid theory equation of state; Phase behavior; Methyl alcohol; Methanol
• ISSN: 0896-8446; 1872-8162
• DOI: 10.1016/j.supflu.2011.12.013

[Display omitted] ► Vapor–liquid equilibrium data for methanol+propylene mixture was measured experimentally. ► Statistical associating fluid theory and Soave–Redlich–Kwong models were optimized to the experimental results. ► Statistical associating fluid theory gave much better results than Soave–Redlich–Kwong equation of state, especially at higher pressures. The high-pressure vapor–liquid equilibria of methanol+propylene was measured experimentally within a temperature and pressure range of 293–373K and 0.17–3.7MPa, respectively, using a synthetic method. The system showed a highly non-ideal behavior with positive deviation from Raoult's law. The phase behavior was also modeled by the statistical associating fluid theory (SAFT) and the Soave–Redlich–Kwong (SRK) equations of state. The statistical associating fluid theory correlated the phase behavior of the binary system much better than the Soave–Redlich–Kwong model, especially at higher pressures. For example, the average absolute deviation percent (AAD%) at T=370K was 1.11% for the SAFT model with k12=0.02088 and 6.75% for the SRK model with k12=0.08035.