Phase behavior of the carbon dioxide/toluene/poly(ethylene glycol) ternary system

IF 2.8 3区工程技术 Q3 CHEMISTRY, PHYSICAL Fluid Phase Equilibria Pub Date : 2024-09-11 DOI:10.1016/j.fluid.2024.114227

Hiroaki Matsukawa , Ryota Suzuki , Katsuto Otake

{"title":"Phase behavior of the carbon dioxide/toluene/poly(ethylene glycol) ternary system","authors":"Hiroaki Matsukawa , Ryota Suzuki , Katsuto Otake","doi":"10.1016/j.fluid.2024.114227","DOIUrl":null,"url":null,"abstract":"<div>The phase behavior of a carbon dioxide (CO2)/toluene (Tol)/poly(ethylene glycol) (PEG) ternary system was investigated in this study to consider the effect of the polymer species on the phase diagram. Measurements were performed using a synthetic method combined with laser displacement and turbidity measurements. Bubble points (vapor–liquid phase separation) were determined from changes in the piston displacement and cloud points (liquid–liquid (LL) phase separation) were determined from changes in the turbidity. The phase boundaries of the CO2 mass fractions ranging from 0.113 to 0.496 were measured by varying the Tol/PEG mass ratio. The homogeneous phase area decreased when the mass ratio of PEG to Tol increased and/or the temperature decreased. These changes in the LL phase-separation behavior were explained by referring to the free volume fraction and solubility parameter estimated using the Sanchez–Lacombe equation of state. The free volume integral fraction could explain the phase diagram, but not the solubility parameter; the effect of polymer species on the Px phase diagram of the ternary system was explained by considering specific interactions between dissimilar components. These results could promote a comprehensive understanding of the phase diagram of CO2/organic solvent/polymer systems and aid the prediction of phase behavior.</div>","PeriodicalId":12170,"journal":{"name":"Fluid Phase Equilibria","volume":"588 ","pages":"Article 114227"},"PeriodicalIF":2.8000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fluid Phase Equilibria","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378381224002024","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}

引用次数: 0

Abstract

The phase behavior of a carbon dioxide (CO₂)/toluene (Tol)/poly(ethylene glycol) (PEG) ternary system was investigated in this study to consider the effect of the polymer species on the phase diagram. Measurements were performed using a synthetic method combined with laser displacement and turbidity measurements. Bubble points (vapor–liquid phase separation) were determined from changes in the piston displacement and cloud points (liquid–liquid (LL) phase separation) were determined from changes in the turbidity. The phase boundaries of the CO₂ mass fractions ranging from 0.113 to 0.496 were measured by varying the Tol/PEG mass ratio. The homogeneous phase area decreased when the mass ratio of PEG to Tol increased and/or the temperature decreased. These changes in the LL phase-separation behavior were explained by referring to the free volume fraction and solubility parameter estimated using the Sanchez–Lacombe equation of state. The free volume integral fraction could explain the phase diagram, but not the solubility parameter; the effect of polymer species on the Px phase diagram of the ternary system was explained by considering specific interactions between dissimilar components. These results could promote a comprehensive understanding of the phase diagram of CO₂/organic solvent/polymer systems and aid the prediction of phase behavior.

Abstract Image

查看原文

微信好友朋友圈 QQ好友复制链接

本刊更多论文

二氧化碳/甲苯/聚乙二醇三元体系的相行为

本研究调查了二氧化碳（CO2）/甲苯（Tol）/聚乙二醇（PEG）三元体系的相行为，以考虑聚合物种类对相图的影响。测量采用合成法结合激光位移和浊度测量法进行。根据活塞位移的变化确定气泡点（汽液相分离），根据浊度的变化确定浊点（液液（LL）相分离）。通过改变 Tol/PEG 的质量比，测量了二氧化碳质量分数从 0.113 到 0.496 的相界。当 PEG 与 Tol 的质量比增加和/或温度降低时，均相面积减小。LL 相分离行为的这些变化可通过使用 Sanchez-Lacombe 状态方程估算的自由体积分数和溶解度参数来解释。自由体积分数可以解释相图，但不能解释溶解度参数；聚合物种类对三元体系 Px 相图的影响可以通过考虑不同组分之间的特定相互作用来解释。这些结果有助于全面了解二氧化碳/有机溶剂/聚合物体系的相图，并有助于预测相行为。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

求助全文

约1分钟内获得全文去求助

来源期刊

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.