首页> 外文期刊>The Journal of Chemical Thermodynamics >Phase equilibrium data for ternary (carbon dioxide plus dichloromethane plus eugenol) and quaternary systems (carbon dioxide plus dichloromethane plus eugenol plus poly-epsilon-caprolactone)
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Phase equilibrium data for ternary (carbon dioxide plus dichloromethane plus eugenol) and quaternary systems (carbon dioxide plus dichloromethane plus eugenol plus poly-epsilon-caprolactone)

机译:三元(二氧化碳加二氯甲烷加丁香酚)和四元系统(二氧化碳加二氯甲烷加丁香酚加聚ε-己内酯)的相平衡数据

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摘要

Experimental phase equilibrium values for the ternary (carbon dioxide + dichloromethane + eugenol) and quaternary systems (carbon dioxide + dichloromethane + eugenol + poly-epsilon-caprolactone) have been determined in order to provide fundamental information to conduct microencapsulation of eugenol in supercritical carbon dioxide medium. The experiments were performed using a variable-volume view cell over the temperature range from (308.15 to 323.15) K. For the ternary system, three different values of mole ratios eugenol to dichloromethane (1:1, 1:5 and 1:10) were evaluated. Phase transitions of vapour-liquid type bubble point and vapour-liquid type dew point were observed at pressures between (0.73 and 12.43) MPa. Experimental results were modelled using the Peng-Robinson (PR) equation of state with the Wong-Sandler (PR-WS) mixing rule, providing a satisfactory representation of the experimental phase equilibrium data, with an average absolute deviation of 2.61 MPa. For the quaternary system two mole ratios of eugenol to poly-epsilon-caprolactone (PCL) to dicholoromethane (1:0.002:5 and 1:0.004:10) were adopted. For this system, only vapour-liquid phase transitions of the bubble point type were observed. It was observed that an increase in the temperature as well as in PCL concentration increased the transition pressures for these systems evaluated. (C) 2015 Elsevier Ltd. All rights reserved.
机译:确定了三元体系(二氧化碳+二氯甲烷+丁香酚)和四元体系(二氧化碳+二氯甲烷+丁香酚+聚ε-己内酯)的实验相平衡值,以便为在超临界二氧化碳中进行丁香酚的微囊化提供基本信息。中。实验使用的是可变体积的视场,温度范围为(308.15至323.15)K。对于三元体系,丁香酚与二氯甲烷的摩尔比为三种不同的值(1:1、1:5和1:10)被评估。在(0.73和12.43)MPa的压力下观察到汽液型气泡点和汽液型露点的相变。使用Peng-Robinson(PR)状态方程和Wong-Sandler(PR-WS)混合规则对实验结果进行建模,可以令人满意地表示实验相平衡数据,平均绝对偏差为2.61 MPa。对于四元体系,采用丁子香酚与聚ε-己内酯(PCL)与二氯甲烷的摩尔比为2:1(0.002:5和1:0.004:10)。对于该系统,仅观察到了泡点类型的汽-液相转变。观察到温度和PCL浓度的增加都增加了这些评估系统的转变压力。 (C)2015 Elsevier Ltd.保留所有权利。

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