共查询到20条相似文献,搜索用时 0 毫秒
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Density and viscosity of binary mixtures of (x13-amino-1-propanol + x2isobutanol) and (x13-amino-1-propanol + x22-propanol) were measured over the entire composition range and from temperatures (293.15 to 333.15) K at ambient pressure. The excess molar volumes and viscosity deviations were calculated and correlated by the Redlich–Kister (RK) equation. The thermal expansion coefficient and its excess value, isothermal coefficient of excess molar enthalpy, and excess partial molar volumes were determined by using the experimental values of density and are described as a function of composition and temperature. The excess molar volumes are negative over the entire mole fraction range for both mixtures and increase with increasing temperature. The excess molar volumes obtained were correlated by the Prigogine–Flory–Patterson (PFP) model. The viscosity deviations of the binary mixtures are negative over the entire composition range and decrease with increasing temperature. 相似文献
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Jin L. Liu Andrew W. Hakin Gavin R. Hedwig 《The Journal of chemical thermodynamics》2009,41(11):1232-1238
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Densities (ρ) and speeds of sound (u) have been measured for (l-phenylalanine + 0.01 mol · kg−1 aqueous β-cyclodextrin) and (l-histidine + 0.01 mol · kg−1 aqueous β-cyclodextrin) systems at T = (293.15, 298.15, 303.15 and 308.15) K using the density and sound velocity Meter DSA 5000 M. The ρ and u values have been utilized to evaluate values of the partial molar volume (), transfer partial molar volume (), partial molar isentropic compressibility (), and transfer partial molar isentropic compressibility () of the systems studied. The experimentally measured and calculated parameters have been interpreted in terms of host-guest and ion-hydrophilic interactions operative in the systems. 相似文献
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Eugene Olivier Trevor M. Letcher Paramespri Naidoo Deresh Ramjugernath 《The Journal of chemical thermodynamics》2010,42(1):78-83
Activity coefficients at infinite dilution were determined for 24 solutes (n-alkanes, alk-1-enes, alk-1-ynes, cycloalkanes, alkylbenzenes, and alcohols) in the ionic liquid 1-ethyl-3-methylimidazolium trifluoromethanesulfonate by gas-liquid chromatography at three different temperatures T = (313.15, 323.15, 333.15) K. The partial molar excess enthalpy values at infinite dilution were calculated from the experimental results over the same temperature range. Selectivities and capacities at infinite dilution for the hexane/benzene and methanol/benzene separation problems were calculated from experimental infinite dilution activity coefficient values. The activity coefficients, enthalpies, selectivities, and capacities are discussed and compared to literature values for other ionic liquids, as well as industrial molecular solvents. 相似文献
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Eugene Olivier Trevor M. Letcher Paramespri Naidoo Deresh Ramjugernath 《The Journal of chemical thermodynamics》2010,42(5):646-650
Activity coefficients at infinite dilution were determined for 24 solutes: n-alkanes, alk-1-enes, alk-1-ynes, cycloalkanes, alkylbenzenes and alcohols in the ionic liquid 1-octyl-3-methylimidazolium hexafluorophosphate, [OMIM][PF6], by gas–liquid chromatography at three different temperatures T = (313.15, 323.15, and 333.15) K. The partial molar excess enthalpy values at infinite dilution were calculated from the experimental data over the same temperature range. Capacities and selectivities at infinite dilution for the systems hexane/benzene and methanol/benzene were determined from the experimental data and compared to the literature values for other ionic liquids, as well as for industrial molecular solvents. The influence of the cation and anion of the ionic liquid on the activity coefficient is discussed, as well as the usefulness of [OMIM][PF6] in separating organic liquids. 相似文献
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《Physics and Chemistry of Liquids》2012,50(6):535-541
The excess molar volume of the ternary mixture [2-propanol?+?ethyl acetate?+?n-hexane], and its binary constituents; [2-propanol?+?ethyl acetate], [2-propanol?+?n-hexane] and [ethyl acetate?+?n-hexane] were evaluated by the mixtures density measurements over the whole concentration range at three temperatures 298.15, 308.15 and 313.15?K. The excess molar volumes data were fitted to the Redlich–Kister (RK) type equation and the parameters of this equation have been calculated and presented for the studied mixtures. 相似文献
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Eugene Olivier Trevor M. Letcher Paramespri Naidoo Deresh Ramjugernath 《The Journal of chemical thermodynamics》2011,43(6):829-833
Activity coefficients at infinite dilution were determined for 27 solutes: n-alkanes, alk-1-enes, alk-1-ynes, cycloalkanes, alkylbenzenes, alcohols, and ketones in the ionic liquid 1-butyl-3-methylimidazolium hexafluoroantimonate, [BMIM][SbF6], by gas–liquid chromatography at three different temperatures, T = (313.15, 323.15, and 333.15) K. The results are compared to published data on related compounds. The partial molar excess enthalpy values at infinite dilution were calculated from the experimental data over the same temperature range. Selectivities and capacities at infinite dilution were calculated for the hexane/benzene and methanol/benzene systems from experimental infinite dilution activity coefficients and compared to the literature values for related ionic liquids, as well as to data on industrial molecular solvents. 相似文献
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M. Rezaei-Sameti H. Iloukhani M. Rakhshi 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2010,84(12):2023-2032
In this work we used the experimental result for calculating the thermal expansion coefficients α, and their excess values
α
E
, and isothermal coefficient of pressure excess molar enthalpy and comparison the obtain results with Flory theory of liquid
mixtures for the binary mixtures {methanol, ethanol, 1-propanol and 2-butanol-chloroform} at 288.15, 293.15, 298.15, 303.15,
308.15, 313.15, 318.15, and 323.15 K. The excess thermal expansion coefficients α
E
and the isothermal coefficient of pressure excess molar enthalpy ((∂H
mE/∂P)
T,x
for binary mixtures of {methanol and ethanol + chloroform} are S-shaped and for binary mixtures of {1-propanol and 2-butanol
+ chloroform} are positive over the mole fraction. The isothermal coefficient of pressure excess molar enthalpy (∂H
mE/∂P)
T,x
, are negative over the mole fraction range for binary mixture of {1-propanol and 2-butanol + chloroform}. The calculated
values by using the Flory theory of liquid mixtures show a good agreement between the theory and experimental. 相似文献
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《Physics and Chemistry of Liquids》2012,50(2):221-229
Densities, ρ and excess molar volumes, V?E of the binary mixtures of sulfolane, +methanol, +n-propanol,?+n-butanol, and +n-pentanol were measured at temperatures 298.15, 303.15, 308.15, 313.15, and 318.15?K, respectively, covering the whole composition range except methanol at 303.15–323.15?K. The V E for the systems were found to be negative and large in magnitude. The values of V E of the sulfolane, +n-butanol and sulfolane, +n-pentanol mixtures are being positive at lower and higher mole fractions of the alkanols (x 2). The magnitudes of the V E values of the mixtures are in the order sulfolane?+?methanol?>?sulfolane?+?n-propanol?>?sulfolane?+?n-butanol?>?sulfolane?+?n-pentanol. The observed values of V E for the mixtures have been explained in terms of (i) effects due to the differences in chain length of the alcohols, (ii) dipole–dipole interactions between the polar molecules, and (iii) geometric effect due to the differences in molar volume of the component molecules. These are more noticeable in the case of lower alcohols. All these properties have been expressed satisfactorily by appropriate polynomials. 相似文献
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Prashant Reddy Nobuhle V. Gwala Nirmala Deenadayalu Deresh Ramjugernath 《The Journal of chemical thermodynamics》2011,43(5):754-758
In this work, activity coefficients at infinite dilution () have been obtained for 19 polar and non-polar organic solutes in the form of n-alkanes, cycloalkanes, 1-alkenes, 1-alkynes, aromatic compounds, and ketones in the ionic liquid methyl(trioctyl)ammonium thiosalicylate by gas–liquid chromatography at three different temperatures, i.e. T = (303.15, 313.15, and 323.15) K. Two columns with different phase loadings of the ionic liquid in the stationary phase (25% and 30%) were employed to obtain values at each temperature investigated. Partial molar excess enthalpies at infinite dilution () were calculated for each of the solutes from the temperature dependency of the values for the temperature range in this study. Selectivity values at infinite dilution () were computed from the values to screen the potential candidacy of the ionic liquid for the separation of n-hexane/benzene mixtures. The results from this study have been compared to those available for several other classes of ionic liquids and commercial solvents employed in solvent-enhanced industrial separation processes. 相似文献