Xenon Hydrate as an Analog of Methane Hydrate in Geologic Systems Out of Thermodynamic Equilibrium

Methane hydrate occurs naturally under pressure and temperature conditions that are not straightforward to replicate experimentally. Xenon has emerged as an attractive laboratory alternative to methane for studying hydrate formation and dissociation in multiphase systems, given that it forms hydrate...

Full description

Bibliographic Details
Main Authors: Fu, Xiaojing, Waite, William F., Cueto-Felgueroso Landeira, Luis, Juanes, Ruben
Other Authors: Massachusetts Institute of Technology. Department of Civil and Environmental Engineering
Format: Article
Language:English
Published: American Geophysical Union (AGU) 2020
Online Access:https://hdl.handle.net/1721.1/125592
_version_ 1811071441460789248
author Fu, Xiaojing
Waite, William F.
Cueto-Felgueroso Landeira, Luis
Juanes, Ruben
author2 Massachusetts Institute of Technology. Department of Civil and Environmental Engineering
author_facet Massachusetts Institute of Technology. Department of Civil and Environmental Engineering
Fu, Xiaojing
Waite, William F.
Cueto-Felgueroso Landeira, Luis
Juanes, Ruben
author_sort Fu, Xiaojing
collection MIT
description Methane hydrate occurs naturally under pressure and temperature conditions that are not straightforward to replicate experimentally. Xenon has emerged as an attractive laboratory alternative to methane for studying hydrate formation and dissociation in multiphase systems, given that it forms hydrates under milder conditions. However, building reliable analogies between the two hydrates requires systematic comparisons, which are currently lacking. We address this gap by developing a theoretical and computational model of gas hydrates under equilibrium and nonequilibrium conditions. We first compare equilibrium phase behaviors of the Xe·H2O and CH4·H2O systems by calculating their isobaric phase diagram, and then study the nonequilibrium kinetics of interfacial hydrate growth using a phase field model. Our results show that Xe·H2O is a good experimental analog to CH4·H2O, but there are key differences to consider. In particular, the aqueous solubility of xenon is altered by the presence of hydrate, similar to what is observed for methane; but xenon is consistently less soluble than methane. Xenon hydrate has a wider nonstoichiometry region, which could lead to a thicker hydrate layer at the gas-liquid interface when grown under similar kinetic forcing conditions. For both systems, our numerical calculations reveal that hydrate nonstoichiometry coupled with hydrate formation dynamics leads to a compositional gradient across the hydrate layer, where the stoichiometric ratio increases from the gas-facing side to the liquid-facing side. Our analysis suggests that accurate composition measurements could be used to infer the kinetic history of hydrate formation in natural settings where gas is abundant. ©2019. American Geophysical Union. All Rights Reserved.
first_indexed 2024-09-23T08:51:00Z
format Article
id mit-1721.1/125592
institution Massachusetts Institute of Technology
language English
last_indexed 2024-09-23T08:51:00Z
publishDate 2020
publisher American Geophysical Union (AGU)
record_format dspace
spelling mit-1721.1/1255922022-09-30T11:42:50Z Xenon Hydrate as an Analog of Methane Hydrate in Geologic Systems Out of Thermodynamic Equilibrium Fu, Xiaojing Waite, William F. Cueto-Felgueroso Landeira, Luis Juanes, Ruben Massachusetts Institute of Technology. Department of Civil and Environmental Engineering Methane hydrate occurs naturally under pressure and temperature conditions that are not straightforward to replicate experimentally. Xenon has emerged as an attractive laboratory alternative to methane for studying hydrate formation and dissociation in multiphase systems, given that it forms hydrates under milder conditions. However, building reliable analogies between the two hydrates requires systematic comparisons, which are currently lacking. We address this gap by developing a theoretical and computational model of gas hydrates under equilibrium and nonequilibrium conditions. We first compare equilibrium phase behaviors of the Xe·H2O and CH4·H2O systems by calculating their isobaric phase diagram, and then study the nonequilibrium kinetics of interfacial hydrate growth using a phase field model. Our results show that Xe·H2O is a good experimental analog to CH4·H2O, but there are key differences to consider. In particular, the aqueous solubility of xenon is altered by the presence of hydrate, similar to what is observed for methane; but xenon is consistently less soluble than methane. Xenon hydrate has a wider nonstoichiometry region, which could lead to a thicker hydrate layer at the gas-liquid interface when grown under similar kinetic forcing conditions. For both systems, our numerical calculations reveal that hydrate nonstoichiometry coupled with hydrate formation dynamics leads to a compositional gradient across the hydrate layer, where the stoichiometric ratio increases from the gas-facing side to the liquid-facing side. Our analysis suggests that accurate composition measurements could be used to infer the kinetic history of hydrate formation in natural settings where gas is abundant. ©2019. American Geophysical Union. All Rights Reserved. DOE (award no. DE-FE0013999) DOE (award no.DE-SC0018357) DOE Interagency Agreement (DE-FE0023495) Miller Research Fellowship UC Berkeley U.S.Geological Survey's Gas Hydrate Project U.S.Geological Survey Coastal,Marine Hazards and Resources Program Spanish Ministry of Economy and Competitiveness(grant no. RYC-2012-11704) Spanish Ministry of Economy and Competitiveness (grant no. CTM2014-54312-P) MIT International Science and Technology Initiatives (Seed Fund grant) 2020-05-29T21:47:40Z 2020-05-29T21:47:40Z 2019-05 2019-01 2020-05-27T19:54:34Z Article http://purl.org/eprint/type/JournalArticle 1525-2027 https://hdl.handle.net/1721.1/125592 Fu, Xiaojing et al., "Xenon Hydrate as an Analog of Methane Hydrate in Geologic Systems Out of Thermodynamic Equilibrium." Geochemistry, Geophysics, Geosystems 20, 5 (May 2019): 2462-72 doi. 10.1029/2019GC008250 ©2019 Authors en https://dx.doi.org/10.1029/2019GC008250 Geochemistry, Geophysics, Geosystems Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. application/pdf American Geophysical Union (AGU) Other repository
spellingShingle Fu, Xiaojing
Waite, William F.
Cueto-Felgueroso Landeira, Luis
Juanes, Ruben
Xenon Hydrate as an Analog of Methane Hydrate in Geologic Systems Out of Thermodynamic Equilibrium
title Xenon Hydrate as an Analog of Methane Hydrate in Geologic Systems Out of Thermodynamic Equilibrium
title_full Xenon Hydrate as an Analog of Methane Hydrate in Geologic Systems Out of Thermodynamic Equilibrium
title_fullStr Xenon Hydrate as an Analog of Methane Hydrate in Geologic Systems Out of Thermodynamic Equilibrium
title_full_unstemmed Xenon Hydrate as an Analog of Methane Hydrate in Geologic Systems Out of Thermodynamic Equilibrium
title_short Xenon Hydrate as an Analog of Methane Hydrate in Geologic Systems Out of Thermodynamic Equilibrium
title_sort xenon hydrate as an analog of methane hydrate in geologic systems out of thermodynamic equilibrium
url https://hdl.handle.net/1721.1/125592
work_keys_str_mv AT fuxiaojing xenonhydrateasananalogofmethanehydrateingeologicsystemsoutofthermodynamicequilibrium
AT waitewilliamf xenonhydrateasananalogofmethanehydrateingeologicsystemsoutofthermodynamicequilibrium
AT cuetofelguerosolandeiraluis xenonhydrateasananalogofmethanehydrateingeologicsystemsoutofthermodynamicequilibrium
AT juanesruben xenonhydrateasananalogofmethanehydrateingeologicsystemsoutofthermodynamicequilibrium