Methane hydrate thermodynamic phase stability predictions in the presence of salt inhibitors and their mixture for offshore operations

A thermodynamic model is developed and used in this study to predict the phase equilibrium conditions of a methane -aqueous salt inhibitor -water hydrate system. The modified van der Waals-Platteeuw (vdWP) model is used to calculate the equilibrium condition of the hydrate phase. To compute the fuga...

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Autores principales: Venkata Ramana Avula, Venkata Swamy Nalajala, Golamari Siva Reddy, M.J.A. Prince
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/ddf46612924e489689be658de53add78
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spelling oai:doaj.org-article:ddf46612924e489689be658de53add782021-11-20T05:16:16ZMethane hydrate thermodynamic phase stability predictions in the presence of salt inhibitors and their mixture for offshore operations2667-312610.1016/j.ctta.2021.100022https://doaj.org/article/ddf46612924e489689be658de53add782021-09-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2667312621000195https://doaj.org/toc/2667-3126A thermodynamic model is developed and used in this study to predict the phase equilibrium conditions of a methane -aqueous salt inhibitor -water hydrate system. The modified van der Waals-Platteeuw (vdWP) model is used to calculate the equilibrium condition of the hydrate phase. To compute the fugacities of gas and liquid phases, the Peng-Robinson equation of state (PR-EoS) and a previously developed Pitzer-Mayorga-Zavitsas-hydration model are used. The model predictions are compared to experimental results on methane hydrate phase equilibrium in the presence of an aqueous salt inhibitor. The absolute average relative deviation in predicted methane -aqueous salt inhibitor -water hydrate equilibrium pressure (AARD-P%) with the developed Pitzer-Mayorga-Zavitsas-Hydration model is 3.59% for CH4+NaCl, 1.52% for CH4+KCl, and 2.70% for CH4+ CaCl2. Finally, the hydrate suppression temperature caused by aqueous salt inhibitors and their mixtures on methane hydrate phase stability is calculated, and it is CaCl2>KCl>NaCl in that order. This work's phase equilibrium model demonstrates the potential application of determining methane hydrate equilibrium conditions in the presence of aqueous salt inhibitors and their mixtures used in offshore oil field applications.Venkata Ramana AvulaVenkata Swamy NalajalaGolamari Siva ReddyM.J.A. PrinceElsevierarticleGas hydrateInhibitorsMethanePhase equilibriumAqueous salt inhibitorsThermodynamicsQC310.15-319ENChemical Thermodynamics and Thermal Analysis, Vol 3, Iss , Pp 100022- (2021)
institution DOAJ
collection DOAJ
language EN
topic Gas hydrate
Inhibitors
Methane
Phase equilibrium
Aqueous salt inhibitors
Thermodynamics
QC310.15-319
spellingShingle Gas hydrate
Inhibitors
Methane
Phase equilibrium
Aqueous salt inhibitors
Thermodynamics
QC310.15-319
Venkata Ramana Avula
Venkata Swamy Nalajala
Golamari Siva Reddy
M.J.A. Prince
Methane hydrate thermodynamic phase stability predictions in the presence of salt inhibitors and their mixture for offshore operations
description A thermodynamic model is developed and used in this study to predict the phase equilibrium conditions of a methane -aqueous salt inhibitor -water hydrate system. The modified van der Waals-Platteeuw (vdWP) model is used to calculate the equilibrium condition of the hydrate phase. To compute the fugacities of gas and liquid phases, the Peng-Robinson equation of state (PR-EoS) and a previously developed Pitzer-Mayorga-Zavitsas-hydration model are used. The model predictions are compared to experimental results on methane hydrate phase equilibrium in the presence of an aqueous salt inhibitor. The absolute average relative deviation in predicted methane -aqueous salt inhibitor -water hydrate equilibrium pressure (AARD-P%) with the developed Pitzer-Mayorga-Zavitsas-Hydration model is 3.59% for CH4+NaCl, 1.52% for CH4+KCl, and 2.70% for CH4+ CaCl2. Finally, the hydrate suppression temperature caused by aqueous salt inhibitors and their mixtures on methane hydrate phase stability is calculated, and it is CaCl2>KCl>NaCl in that order. This work's phase equilibrium model demonstrates the potential application of determining methane hydrate equilibrium conditions in the presence of aqueous salt inhibitors and their mixtures used in offshore oil field applications.
format article
author Venkata Ramana Avula
Venkata Swamy Nalajala
Golamari Siva Reddy
M.J.A. Prince
author_facet Venkata Ramana Avula
Venkata Swamy Nalajala
Golamari Siva Reddy
M.J.A. Prince
author_sort Venkata Ramana Avula
title Methane hydrate thermodynamic phase stability predictions in the presence of salt inhibitors and their mixture for offshore operations
title_short Methane hydrate thermodynamic phase stability predictions in the presence of salt inhibitors and their mixture for offshore operations
title_full Methane hydrate thermodynamic phase stability predictions in the presence of salt inhibitors and their mixture for offshore operations
title_fullStr Methane hydrate thermodynamic phase stability predictions in the presence of salt inhibitors and their mixture for offshore operations
title_full_unstemmed Methane hydrate thermodynamic phase stability predictions in the presence of salt inhibitors and their mixture for offshore operations
title_sort methane hydrate thermodynamic phase stability predictions in the presence of salt inhibitors and their mixture for offshore operations
publisher Elsevier
publishDate 2021
url https://doaj.org/article/ddf46612924e489689be658de53add78
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AT golamarisivareddy methanehydratethermodynamicphasestabilitypredictionsinthepresenceofsaltinhibitorsandtheirmixtureforoffshoreoperations
AT mjaprince methanehydratethermodynamicphasestabilitypredictionsinthepresenceofsaltinhibitorsandtheirmixtureforoffshoreoperations
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