2013
DOI: 10.1016/j.fluid.2013.03.002
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Liquid–liquid equilibria for the ternary system (water+hexadecane+dipropylene glycol n-propyl ether)

Abstract: a b s t r a c tThe fish-shaped phase diagram of the ternary system (water + hexadecane + dipropylene glycol n-propyl ether) under atmospheric pressure was performed at constant water/hexadecane mass ratio (1/1). The upper critical solution temperature of the ternary system was determined as 314.00 K. Liquid + liquid equilibria of the system were measured at T = 298.15, 308.15, and 318.15 K under atmospheric pressure. The experimental data of liquid-liquid equilibria were further correlated with the NRTL model.

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Cited by 14 publications
(14 citation statements)
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“…It is well understood that the glycol ether mainly dissolves in the oil-rich phase when the system temperature is above its UCST. [1][2][3][4][5]7,9 The experimental equilibrium compositions of the ternary system water + dodecane + C 3 P 2 at (288.15, 298.15, and 308.15) K are given in Tables 1, 2, and 3, respectively. The LCST of the binary water + C 3 P 2 system is 283.15 K, 3 and the water + C 3 P 2 mixture is not completely miscible at these three temperatures.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
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“…It is well understood that the glycol ether mainly dissolves in the oil-rich phase when the system temperature is above its UCST. [1][2][3][4][5]7,9 The experimental equilibrium compositions of the ternary system water + dodecane + C 3 P 2 at (288.15, 298.15, and 308.15) K are given in Tables 1, 2, and 3, respectively. The LCST of the binary water + C 3 P 2 system is 283.15 K, 3 and the water + C 3 P 2 mixture is not completely miscible at these three temperatures.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…The ternary mixtures with different C 3 P 2 mass fractions were prepared under the condition of constant water to dodecane mass ratio at 1:1. All samples sealed in test tubes were mixed completely and then were put in a homemade thermostat (its temperature was controlled within ± 0.005 K) to allow the samples for equilibration under a prescribed temperature. When the system reached equilibrium, liquid phases were thoroughly transparent, and interfaces were very sharp and looked like a mirror.…”
Section: Methodsmentioning
confidence: 99%
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“…Liquid–liquid equilibria (LLE) data is the foundation of extraction. LLE data of systems containing higher alcohols + higher hydrocarbons + water or ethanol have been studied in recent years. However, the LLE data related to ethanol (1) + octanol (2) + nonanol (3) + dodecane (4) + tridecane (5) + water (6) has not been reported. In this work, experimental liquid–liquid equilibria data of four quaternary systems {ethanol (1) + octanol (2) + dodecane (4) + water (6)}, {ethanol (1) + octanol (2) + tridecane (5) + water (6)}, {ethanol (1) + nonanol (3) + dodecane (4) + water (6)}, and {ethanol (1) + nonanol (3) + tridecane (5) + water (6)} were determined at T of 293.15, 298.15, and 303.15 K and P of 101.3 kPa.…”
Section: Introductionmentioning
confidence: 99%