{"title":"A semi-theoretical phase equilibrium equation for methane hydrate accounting for physicochemical properties and inter-grain arrangement of sediment","authors":"Xudong Zhang , Mingjing Jiang , Huaning Wang","doi":"10.1016/j.fluid.2025.114463","DOIUrl":null,"url":null,"abstract":"<div><div>The phase equilibrium equation for methane hydrate (MH) is influenced by the pore size within soils and the physicochemical properties of the soil minerals. Therefore, we presented a semi-theoretical phase equilibrium equation for MH in sediments that accounts for both pore size and physicochemical characteristics. First, we examined the relationship between pore size and sample porosity, interparticle angles, and the shape of interparticle cementation. Subsequently, we characterized the relationships among pore size, water content, and the new phase equilibrium equation, considering capillary pressure and bound water content. Finally, we validated the phase equilibrium equation with experimental data available in the literature. Our findings indicate that low water content inhibits hydrate formation, while greater pore sizes enhance MH formation. Additionally, a simultaneous reduction in both pore size and water content significantly inhibits hydrate formation.</div></div>","PeriodicalId":12170,"journal":{"name":"Fluid Phase Equilibria","volume":"597 ","pages":"Article 114463"},"PeriodicalIF":2.7000,"publicationDate":"2025-05-06","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/S0378381225001335","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 equilibrium equation for methane hydrate (MH) is influenced by the pore size within soils and the physicochemical properties of the soil minerals. Therefore, we presented a semi-theoretical phase equilibrium equation for MH in sediments that accounts for both pore size and physicochemical characteristics. First, we examined the relationship between pore size and sample porosity, interparticle angles, and the shape of interparticle cementation. Subsequently, we characterized the relationships among pore size, water content, and the new phase equilibrium equation, considering capillary pressure and bound water content. Finally, we validated the phase equilibrium equation with experimental data available in the literature. Our findings indicate that low water content inhibits hydrate formation, while greater pore sizes enhance MH formation. Additionally, a simultaneous reduction in both pore size and water content significantly inhibits hydrate formation.
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.