Abstract
In this work the isobaric vapor−liquid equilibrium (VLE) data for hexane + 1-decene and octane + 1-decene systems have been measured at 101.33 kPa. The results were correlated using the Margules, Van Laar, Wilson, and UNIQUAC equations for the liquid phase activity coefficients. The average deviations fall within the same range for all models and agree well with experimental VLE data obtained in this work. Also, the experimental results were compared with the predictions of the modified UNIFAC group contribution method, which suggests that UNIFAC works well for unbranched alkane + 1-alkene systems.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
