首页> 外文期刊>Fuel >Experimental measurements and theoretical modeling of high-pressure mass densities and interfacial tensions of carbon dioxide + n-heptane + toluene and its carbon dioxide binary systems
【24h】

Experimental measurements and theoretical modeling of high-pressure mass densities and interfacial tensions of carbon dioxide + n-heptane + toluene and its carbon dioxide binary systems

机译:二氧化碳+正庚烷+甲苯及其二氧化碳二元体系的高压质量密度和界面张力的实验测量和理论模型

获取原文
获取原文并翻译 | 示例
           

摘要

Experimental determination and theoretical predictions of the isothermal (344.15 K) mass densities and interfacial tensions for the system carbon dioxide (CO2) with heptol (n-heptane + toluene) mixtures varying liquid volume fraction compositions of toluene (0, 25, 50, 75, 100% v/v) and over the pressure range 0.1-8 MPa are reported. Measurements are carried out on a high-pressure device that includes a vibrating tube densimeter and a pendant drop tensiometer. Theoretical modeling of mass densities phase equilibria and interfacial properties (i.e., interfacial tension and interfacial concentration profiles) are performed by employing the Square Gradient Theory using an extension of the Statistical Associating Fluid Theory equation of state that accounts for ring fluids. The experimental bulk phase equilibrium densities and interfacial tensions obtained are in very good agreement with the theoretical predictions. Although there are no previous experimental data of these mixtures at the conditions explored herein, the results follow the same trends observed from experimental data at other conditions. The combination of experimental and modeling approaches provides a route to simultaneously predict phase equilibrium and interfacial properties within acceptable statistical deviations. For the systems and conditions studied here, we observe that the phase equilibrium of the mixtures display zeotropic vapor-liquid equilibria with positive deviations from ideal behavior. The mass bulk densities behave ordinarily whereas the interfacial tensions decrease as the pressure or liquid mole fraction of CO2 increases and/or the ratio toluene/heptane decreases. The interfacial concentration along the interfacial region exhibits a remarkable high excess adsorption of CO2, which increases with pressure and it is larger in n-heptane than in toluene. Toluene does not exhibit any special adsorption activity whereas n-heptane displays surface activity only at low pressure in a very narrow range for the case of CO2 +(25% n-heptane + 75% toluene) mixture.
机译:甲苯(0、25、50、75)的液体体积分数组成不同的系统二氧化碳(CO2)与庚醇(正庚烷+甲苯)混合物的等温(344.15 K)质量密度和界面张力的实验确定和理论预测,报道了100%v / v)和超过0.1-8 MPa的压力范围。测量是在高压设备上进行的,该设备包括振动管密度计和悬垂式张力计。质量密度相平衡和界面特性(即界面张力和界面浓度曲线)的理论模型是通过使用平方梯度理论进行的,该理论使用了统计环流理论状态方程的扩展来解释环状流体。获得的实验体相平衡密度和界面张力与理论预测非常吻合。尽管在本文探讨的条件下没有这些混合物的先前实验数据,但结果遵循在其他条件下从实验数据观察到的相同趋势。实验方法和建模方法的组合提供了一种在可接受的统计偏差范围内同时预测相平衡和界面性质的途径。对于此处研究的系统和条件,我们观察到混合物的相平衡显示出共沸汽液相平衡,与理想行为之间存在正偏差。质量堆积密度通常表现为,而界面张力随着CO 2的压力或液体摩尔分数的增加和/或甲苯/庚烷之比的降低而降低。沿界面区域的界面浓度表现出显着的过量过量CO2吸附,CO2随压力而增加,在正庚烷中比在甲苯中大。甲苯没有表现出任何特殊的吸附活性,而正庚烷仅在CO 2 +(25%正庚烷+ 75%甲苯)混合物的低压下在很窄的范围内显示表面活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号