An experimental investigation on the solubility of methane in 1-octanol and n-dodecane at ambient temperatures

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• 作者：Arne Bö ; ttger¹ ; Á ; lvaro Pé ; rez-Salado Kamps ; ^{apsalado@web.de" class="auth_mail" title="E-mail the corresponding author} ; Gerd Maurer
• 关键词：Gas solubility ; Methane ; 1-Octanol ; n-Dodecane ; Henry's constant ; Partial molar volume ; Solvent fraction in vapour phase
• 刊名：Fluid Phase Equilibria
• 出版年：2016
• 出版时间：15 November 2016
• 年：2016
• 卷：427
• 期：Complete
• 页码：566-574
• 全文大小：635 K

文摘

The synthetic method is used for the determination of the liquid phase solubility of methane in 1-octanol at three temperatures (273.25, 283.15, and 293.2) K and of methane in n-dodecane at 273.1 K at pressures up to about 10 MPa. The new gas solubility data is applied to evaluate the molality scale based Henry's constant of methane in those solvents: (4.31, 4.67, and 4.81 ± 0.05) MPa in 1-octanol and (2.75 ± 0.04) MPa in n-dodecane at the given temperatures, respectively. The experimental technique provides as well the density of the gas-saturated liquid phase and thus allows for evaluation of the partial molar volume of methane at infinite dilution in the solvent: (47, 49, and 49 ± 5) cm³/mol in 1-octanol and (45 ± 5) cm³/mol in n-dodecane, respectively. The experimental results are compared with the limited data from the open literature. At the investigated temperatures, the vapour phase can be treated as pure methane, and the extended Henry's law suffices to accurately correlate the new gas solubility data. However, that vapour-liquid equilibrium model is here expanded allowing to accurately predict the small vapour phase solubility of the solvent in compressed methane which is demonstrated by comparison with experimental data from the literature.