{"title":"A deep investigation of neo-pentane freeze-out in methane","authors":"Marco Campestrini, Salem Hoceini, Paolo Stringari","doi":"10.1016/j.fluid.2025.114517","DOIUrl":null,"url":null,"abstract":"<div><div>The investigation of the phase equilibrium behaviour of the methane + neopentane system has attracted a lot of interest in recent years seeing that neopentane is one of the heaviest natural gas components, a characteristic that poses a risk of freeze-out for the natural gas liquefaction process. Despite its high triple-point temperature (256.6 K), the solubility of solid neopentane in liquid methane is expected to be relatively high (a few percent at LNG temperatures) according to recent works dealing with the measurement and prediction of the solid-liquid(-vapor) equilibrium behaviour of this mixture. However, experimental phase equilibrium data are only available at temperatures down to 200 K or below 125 K, meaning that information is still missing in the 125 <em>K</em> < <em>T</em> < 200 K range. The aim of this work is to enhance the understanding of the thermodynamic behaviour of the methane + neopentane system by further experimental results concerning the solid-liquid, solid-vapor, solid-liquid-vapor, and vapor-liquid equilibria between 100 K and 240 K. If the results presented in this work confirm that neopentane is quite soluble in the liquid phase, they also indicate that the liquefaction pressure should be carefully chosen since neopentane is poorly soluble in vapor methane.-</div></div>","PeriodicalId":12170,"journal":{"name":"Fluid Phase Equilibria","volume":"598 ","pages":"Article 114517"},"PeriodicalIF":2.8000,"publicationDate":"2025-06-20","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/S0378381225001876","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 investigation of the phase equilibrium behaviour of the methane + neopentane system has attracted a lot of interest in recent years seeing that neopentane is one of the heaviest natural gas components, a characteristic that poses a risk of freeze-out for the natural gas liquefaction process. Despite its high triple-point temperature (256.6 K), the solubility of solid neopentane in liquid methane is expected to be relatively high (a few percent at LNG temperatures) according to recent works dealing with the measurement and prediction of the solid-liquid(-vapor) equilibrium behaviour of this mixture. However, experimental phase equilibrium data are only available at temperatures down to 200 K or below 125 K, meaning that information is still missing in the 125 K < T < 200 K range. The aim of this work is to enhance the understanding of the thermodynamic behaviour of the methane + neopentane system by further experimental results concerning the solid-liquid, solid-vapor, solid-liquid-vapor, and vapor-liquid equilibria between 100 K and 240 K. If the results presented in this work confirm that neopentane is quite soluble in the liquid phase, they also indicate that the liquefaction pressure should be carefully chosen since neopentane is poorly soluble in vapor methane.-
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.