Experimental determination and theoretical modeling of isobaric vapor–liquid equilibria, liquid mass density, surface tension and dynamic viscosity for the methyl butyrate and tert-butanol binary mixture

IF 2.8 3区 工程技术 Q3 CHEMISTRY, PHYSICAL
Juan M. Uceda, Melissa Morales, Marcela Cartes, Andrés Mejía
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Abstract

The purpose of this work is to provide consistent experimental measurements on the vapor–liquid equilibria (VLE) at the isobaric conditions of 50.00, 75.00 and 94.00 kPa, as well as experimental determinations of the liquid mass densities, the surface tensions and the dynamic viscosities at 298.15 K and 101.3 kPa of the methyl butyrate + tert-butanol binary system within the whole composition range. For these goals, a Gillespie-type cell is used to carry out the VLE measurements, whereas an oscillating densimeter, a maximum differential bubble pressure tensiometer, and a rotating viscometer are used to quantify the remaining physical properties. The thermodynamical quality of the reported VLE data is validated by Fredenslund’s consistency test. Based on the VLE results, this zeotropic binary mixture exhibits a positive deviation from Raoult’s law. Furthermore, the validated data are correlated with three activity coefficient models (i.e., Wilson, NRTL, and UNIQUAC), with the Wilson equation being the most accurate one. Excess volumes, surface tensions, and liquid viscosities data are correlated by Redlich–Kister-type expansions, and the Grunberg–Nissan equation is also applied to viscosity modeling. The calculated excess volumes display a positive deviation from the ideal solution model. Regarding surface tensions, this system showcases both negative and positive deviation, althouhg slight, from the linear behavior while exhibiting the linear trend at a molar fraction of methyl butyrate of 0.758. In addition, this bimodal deviation is adequately predicted by the Chunxi model with the Wilson parameters determined from the VLE data. Finally, the dynamic viscosities data obey a strictly monotonic mole dependence predicted by Eyring’s theory, although without high accuracy. These results also reflect some interesting phenomena related to competitive association effects, which are discussed.

Abstract Image

丁酸甲酯和叔丁醇二元混合物的等压汽液平衡、液体质量密度、表面张力和动态粘度的实验测定和理论建模
这项工作的目的是在 50.00、75.00 和 94.00kPa 等压条件下对汽液平衡(VLE)进行一致的实验测量,并在 298.15K 和 101.3kPa 的整个成分范围内对丁酸甲酯 + 丁醇二元体系的液体质量密度、表面张力和动态粘度进行实验测定。为了实现这些目标,使用 Gillespie 型样品池进行 VLE 测量,而使用振荡密度计、最大气泡压差张力计和旋转粘度计来量化其余物理性质。报告的 VLE 数据的热力学质量通过 Fredenslund 一致性测试进行了验证。根据 VLE 结果,这种各向同性二元混合物与 Raoult 定律存在正偏差。此外,验证数据还与三种活性系数模型(威尔逊、NRTL 和 UNIQUAC)相关联,其中威尔逊方程最为精确。过剩体积、表面张力和液体粘度数据与 Redlich-Kister 型展开式相关联,Grunberg-Nissan 方程也被用于粘度建模。计算得出的过剩体积与理想溶液模型存在正偏差。在表面张力方面,该体系显示出与线性行为的负偏差和正偏差,尽管偏差很小,但在丁酸甲酯的摩尔分数为 0.758 时呈现出线性趋势。此外,根据 VLE 数据确定的 Wilson 参数,春熙模型可以充分预测这种双峰偏差。最后,动态粘度数据符合艾林理论所预测的严格的单调分子依赖性,尽管精确度不高。这些结果还反映了一些与竞争关联效应有关的有趣现象,我们将对此进行讨论。
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来源期刊
Fluid Phase Equilibria
Fluid Phase Equilibria 工程技术-工程:化工
CiteScore
5.30
自引率
15.40%
发文量
223
审稿时长
53 days
期刊介绍: Fluid Phase Equilibria publishes high-quality papers dealing with experimental, theoretical, and applied research related to equilibrium and transport properties of fluids, solids, and interfaces. Subjects of interest include physical/phase and chemical equilibria; equilibrium and nonequilibrium thermophysical properties; fundamental thermodynamic relations; and stability. The systems central to the journal include pure substances and mixtures of organic and inorganic materials, including polymers, biochemicals, and surfactants with sufficient characterization of composition and purity for the results to be reproduced. Alloys are of interest only when thermodynamic studies are included, purely material studies will not be considered. In all cases, authors are expected to provide physical or chemical interpretations of the results. Experimental research can include measurements under all conditions of temperature, pressure, and composition, including critical and supercritical. Measurements are to be associated with systems and conditions of fundamental or applied interest, and may not be only a collection of routine data, such as physical property or solubility measurements at limited pressures and temperatures close to ambient, or surfactant studies focussed strictly on micellisation or micelle structure. Papers reporting common data must be accompanied by new physical insights and/or contemporary or new theory or techniques.
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