Isobaric heat capacities of liquefied natural gas (LNG) mixtures by differential scanning calorimetry at temperatures from 116 K to 150 K and pressures up to 6.90 MPa

• A differential scanning calorimeter was utilized for cryogenic heat capacity experiments. • Liquefied natural gas mixtures were investigated at the relevant ( T , p ) conditions. • The GERG-2008 EOS/EOS-LNG describes the generated results best. The isobaric heat capacity ( c p ) is a crucial thermodynamic property for LNG industries in process design and optimization. Reliable c p results can be applied to validate and improve the equation of state performance under relevant industry conditions. Here, we report the results of c p measurements performed for eight LNG mixtures between (116.3 to 150.3) K and pressures ranging to 6.90 MPa. The results achieved were compared against four thermodynamic models: the fundamental equation of state (EOS) for liquefied natural gas (EOS-LNG), the Peng-Robinson (PR) cubic EOS widely applied in process design, the Lee-Kesler-Plöcker (LKP) EOS, which is reliable for gas enthalpy computation, and the Statistical Associating Fluid Theory (SAFT)-γ Mie EOS integrating contributions from functional groups. The EOS-LNG, which is equivalent for the mixtures investigated in this work to the GERG-2008 Helmholtz equation of state, can satisfactorily compute all the measured heat capacities. The SAFT-γ Mie EOS exhibits excellent accuracy when the correct ideal gas heat capacity correlation is implemented. On the contrary, the PR and LKP EOS show systematic deviations as a function of density, which stem from poor residual heat capacity predictions for the pure constituents and binary mixtures.

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Publication Details

Journal
Fuel
Published
2024-09-26
DOI
https://doi.org/10.1016/j.fuel.2024.132947
Citations
6
Primary Topic
Phase Equilibria and Thermodynamics
Type
article
Field-Weighted Citation Impact
1.11
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article

Isobaric heat capacities of liquefied natural gas (LNG) mixtures by differential scanning calorimetry at temperatures from 116 K to 150 K and pressures up to 6.90 MPa

Eric F. May, Markus Richter, Xiong Xiao
6 citations
Fuel
Phase Equilibria and Thermodynamics
1.11
article

Isobaric heat capacities of liquefied natural gas (LNG) mixtures by differential scanning calorimetry at temperatures from 116 K to 150 K and pressures up to 6.90 MPa

Eric F. May, Markus Richter, Xiong Xiao
article en
6 citations

Abstract

• A differential scanning calorimeter was utilized for cryogenic heat capacity experiments. • Liquefied natural gas mixtures were investigated at the relevant ( T , p ) conditions. • The GERG-2008 EOS/EOS-LNG describes the generated results best. The isobaric heat capacity ( c p ) is a crucial thermodynamic property for LNG industries in process design and optimization. Reliable c p results can be applied to validate and improve the equation of state performance under relevant industry conditions. Here, we report the results of c p measurements performed for eight LNG mixtures between (116.3 to 150.3) K and pressures ranging to 6.90 MPa. The results achieved were compared against four thermodynamic models: the fundamental equation of state (EOS) for liquefied natural gas (EOS-LNG), the Peng-Robinson (PR) cubic EOS widely applied in process design, the Lee-Kesler-Plöcker (LKP) EOS, which is reliable for gas enthalpy computation, and the Statistical Associating Fluid Theory (SAFT)-γ Mie EOS integrating contributions from functional groups. The EOS-LNG, which is equivalent for the mixtures investigated in this work to the GERG-2008 Helmholtz equation of state, can satisfactorily compute all the measured heat capacities. The SAFT-γ Mie EOS exhibits excellent accuracy when the correct ideal gas heat capacity correlation is implemented. On the contrary, the PR and LKP EOS show systematic deviations as a function of density, which stem from poor residual heat capacity predictions for the pure constituents and binary mixtures.

FuelVol. 381
The University of Western Australia (AU), Chemnitz University of Technology (DE), ARC Centre of Excellence in Plant Energy Biology (AU)
Openalex Percentile: Top 24%
Phase Equilibria and Thermodynamics
1.11
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