{"title":"A stable solution method for natural gas density across a wide temperature range using the GERG-2008 equation of state","authors":"Wenlong Jia, Xiujuan Wang, Xia Wu, Changjun Li, Fan Yang, Yupeng Liao","doi":"10.1016/j.fluid.2024.114328","DOIUrl":null,"url":null,"abstract":"<div><div>The GERG-2008 Equation of State (EoS) is recommended by ISO 20765–2 for computing the physical properties of natural gas. Due to the non-monotonic relationship between pressure and molar density described by the GERG-2008 EoS under low temperature conditions, multiple density solutions may exist, making the precise determination of density challenging. This paper first investigates the variation of molar densities with pressure at different temperatures. When the temperature is above <span><math><mrow><msub><mi>T</mi><mi>r</mi></msub><mrow><mo>(</mo><mi>x</mi><mo>)</mo></mrow><mspace></mspace></mrow></math></span>(The composition-dependent reducing functions of the mixture temperature), the pressure described by the GERG-2008 EoS increases monotonically with the molar density, and only one molar density solution that satisfies the equation exists. However, when the temperature is below <span><math><mrow><msub><mi>T</mi><mi>r</mi></msub><mrow><mo>(</mo><mi>x</mi><mo>)</mo></mrow><mspace></mspace></mrow></math></span>, the pressure described by GERG-2008 EoS no longer changes monotonically with the increase in molar density, resulting in multiple molar density solutions that satisfy the equation. To address this problem, this paper proposes a novel solution method that employs a combination of one-dimensional search and the Newton-Raphson iteration to obtain the required molar density solutions. The true molar density solution is then determined based on the Gibbs free energy criterion, ensuring the correct molar density solution is obtained across a wide temperature range. A total of 903 sets of natural gas density data, covering pressures from 0 to 200 MPa and temperatures from 100 to 450 K, were used to validate this method. The computational results indicate that, when the temperature is above<span><math><mrow><msub><mi>T</mi><mi>r</mi></msub><mrow><mo>(</mo><mi>x</mi><mo>)</mo></mrow><mspace></mspace></mrow></math></span>, the average relative deviation (ARD) between the calculated density values and the experimental values ranges from 0.1 % to 0.59 %. For temperatures below <span><math><mrow><msub><mi>T</mi><mi>r</mi></msub><mrow><mo>(</mo><mi>x</mi><mo>)</mo></mrow><mspace></mspace></mrow></math></span>, the ARD values using this method range from 0.01 % to 0.39 %. The proposed solution method enhances the stability and accuracy of solving the GERG-2008 equation, particularly for natural gas at low temperatures.</div></div>","PeriodicalId":12170,"journal":{"name":"Fluid Phase Equilibria","volume":"593 ","pages":"Article 114328"},"PeriodicalIF":2.8000,"publicationDate":"2025-01-07","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/S0378381224003030","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 GERG-2008 Equation of State (EoS) is recommended by ISO 20765–2 for computing the physical properties of natural gas. Due to the non-monotonic relationship between pressure and molar density described by the GERG-2008 EoS under low temperature conditions, multiple density solutions may exist, making the precise determination of density challenging. This paper first investigates the variation of molar densities with pressure at different temperatures. When the temperature is above (The composition-dependent reducing functions of the mixture temperature), the pressure described by the GERG-2008 EoS increases monotonically with the molar density, and only one molar density solution that satisfies the equation exists. However, when the temperature is below , the pressure described by GERG-2008 EoS no longer changes monotonically with the increase in molar density, resulting in multiple molar density solutions that satisfy the equation. To address this problem, this paper proposes a novel solution method that employs a combination of one-dimensional search and the Newton-Raphson iteration to obtain the required molar density solutions. The true molar density solution is then determined based on the Gibbs free energy criterion, ensuring the correct molar density solution is obtained across a wide temperature range. A total of 903 sets of natural gas density data, covering pressures from 0 to 200 MPa and temperatures from 100 to 450 K, were used to validate this method. The computational results indicate that, when the temperature is above, the average relative deviation (ARD) between the calculated density values and the experimental values ranges from 0.1 % to 0.59 %. For temperatures below , the ARD values using this method range from 0.01 % to 0.39 %. The proposed solution method enhances the stability and accuracy of solving the GERG-2008 equation, particularly for natural gas at low temperatures.
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.