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Physical–Chemical Properties of Compressible Clathrates: A Natural Pressure Shift by Extending the van der Waals and Platteeuw Model
We have developed a new model for compressible clathrates that extends the well-known van der Waals and Platteeuw model. The new model is derived by dispensing with the assumption of constant cage radii in the partition function level, resulting in new thermodynamically consistent expressions relati...
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Published in: | Journal of physical chemistry. C 2022-02, Vol.126 (5), p.2839-2856 |
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container_title | Journal of physical chemistry. C |
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creator | Viana Segtovich, Iuri Soter de Azevedo Medeiros, Fernando Tavares, Frederico Wanderley |
description | We have developed a new model for compressible clathrates that extends the well-known van der Waals and Platteeuw model. The new model is derived by dispensing with the assumption of constant cage radii in the partition function level, resulting in new thermodynamically consistent expressions relating the thermodynamic properties of the hydrate phase and the empty lattice isochoric reference. One set of additional parameters to the clathrate modeling framework is introduced, consisting of a scaling factor for each cage radius relative to the edge length of the unit cell. No additional guest-dependent empirical parameters are required. The model exhibits two features not previously reported in the literature: (i) a pressure shift between the clathrate being described and the empty lattice isochoric reference and (ii) differences in the edge length of the unit cell and in the cage radii for different guest species at the same temperature and pressure, as a consequence of the sorption of guests. We also propose a test for thermodynamic consistency at high pressure, based on the multicomponent and multiphase Clapeyron equation. Using this test, we show that the proposed model solves an inconsistency issue observed in phase equilibrium calculations with some of the compressible clathrate models currently in use. We have performed parameter optimization for methane, ethane, and xenon in sI hydrates. Two sets of results are presented: three-phase equilibrium conditions and lattice size versus temperature or pressure for each of these substances, along with available experimental data. |
doi_str_mv | 10.1021/acs.jpcc.1c09715 |
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The new model is derived by dispensing with the assumption of constant cage radii in the partition function level, resulting in new thermodynamically consistent expressions relating the thermodynamic properties of the hydrate phase and the empty lattice isochoric reference. One set of additional parameters to the clathrate modeling framework is introduced, consisting of a scaling factor for each cage radius relative to the edge length of the unit cell. No additional guest-dependent empirical parameters are required. The model exhibits two features not previously reported in the literature: (i) a pressure shift between the clathrate being described and the empty lattice isochoric reference and (ii) differences in the edge length of the unit cell and in the cage radii for different guest species at the same temperature and pressure, as a consequence of the sorption of guests. We also propose a test for thermodynamic consistency at high pressure, based on the multicomponent and multiphase Clapeyron equation. Using this test, we show that the proposed model solves an inconsistency issue observed in phase equilibrium calculations with some of the compressible clathrate models currently in use. We have performed parameter optimization for methane, ethane, and xenon in sI hydrates. Two sets of results are presented: three-phase equilibrium conditions and lattice size versus temperature or pressure for each of these substances, along with available experimental data.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/acs.jpcc.1c09715</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>C: Physical Properties of Materials and Interfaces</subject><ispartof>Journal of physical chemistry. 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The model exhibits two features not previously reported in the literature: (i) a pressure shift between the clathrate being described and the empty lattice isochoric reference and (ii) differences in the edge length of the unit cell and in the cage radii for different guest species at the same temperature and pressure, as a consequence of the sorption of guests. We also propose a test for thermodynamic consistency at high pressure, based on the multicomponent and multiphase Clapeyron equation. Using this test, we show that the proposed model solves an inconsistency issue observed in phase equilibrium calculations with some of the compressible clathrate models currently in use. We have performed parameter optimization for methane, ethane, and xenon in sI hydrates. 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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | C: Physical Properties of Materials and Interfaces |
title | Physical–Chemical Properties of Compressible Clathrates: A Natural Pressure Shift by Extending the van der Waals and Platteeuw Model |
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