Liquid–liquid equilibrium data of water with neohexane,methylcyclohexane, tert-butyl methyl ether,n-heptane and vapor–liquid–liquid equilibrium with methane |
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| Institution: | 1. ISEL — Instituto Superior de Engenharia de Lisboa, Instituto Politécnico de Lisboa, Rua Conselheiro Emídio Navarro 1, 1959-007 Lisbon, Portugal;2. Centro de Física Teórica e Computacional, Faculdade de Ciências da Universidade de Lisboa Campo Grande, Edifício C8, 1749-016 Lisbon, Portugal;1. Institute of Chemical Process Engineering, University of Alicante, 03080, Alicante, Spain;2. Department of Chemical Engineering, University of Alicante, Apdo. 99, 03080, Alicante, Spain;3. CRETUS. Department of Chemical Engineering, Universidade de Santiago de Compostela, E-15782, Santiago de Compostela, Spain;1. Institut für Anorganische und Physikalische Chemie, Fb2 Biologie-Chemie, Universität Bremen, Leobener Str. NWII, 28359 Bremen, Germany;2. Bremen Centre for Computational Materials Science, Universität Bremen, Am Fallturm 1, 28359 Bremen, Germany |
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| Abstract: | Liquid–liquid equilibrium (LLE) data for non-aqueous liquid (neohexane NH], tert-butyl methyl ether TBME], methylcyclohexane MCH], or n-heptane nC7]) and water have been measured under atmospheric pressure at 275.5, 283.15, and 298.15 K. It was found that TBME is the most water soluble followed by NH, MCH, and nC7. As the temperature increased, the solubility of the non-aqueous liquids (NALs) in water decreased. The solubility of water in the non-aqueous liquid was found to increase in the following order: MCH < nC7 < NH < TBME. It was found to increase with increasing temperature. In addition, vapour–liquid–liquid equilibrium (VLLE) data for the above binary systems with methane were measured at 275.5 K and at 120, 1000, and 2000 kPa. It was found that the vapour composition of water and NALs decreased as the pressure increased. The water content in the non-aqueous phase was not a strong function of pressure. The concentration of methane in the non-aqueous phase increased as the pressure increased. Furthermore, the concentration of the methane and NALs in the water phase increased proportionally with pressure. The solubility of methane in water followed Henry's law. It is noted that the measurements were completed prior to the onset of hydrate nucleation. |
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