Plug Formation and Dissociation of Mixed Gas Hydrates and Methane Semi-Clathrate Hydrate Stability

Gas hydrates are known to form plugs in pipelines. Hydrate plug dissociation times can be predicted using the CSMPlug program. At high methane mole fractions of a methane + ethane mixture the predictions agree with experiments for the relative dissociation times of structure I (sI) and structure II...

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Main Author: Hughes, Thomas John
Format: Article in Journal/Newspaper
Language:unknown
Published: University of Canterbury. Chemical and Process Engineering 2008
Subjects:
DSC
Online Access:https://dx.doi.org/10.26021/3369
https://ir.canterbury.ac.nz/handle/10092/1579
id ftdatacite:10.26021/3369
record_format openpolar
spelling ftdatacite:10.26021/3369 2023-05-15T17:12:06+02:00 Plug Formation and Dissociation of Mixed Gas Hydrates and Methane Semi-Clathrate Hydrate Stability Hughes, Thomas John 2008 https://dx.doi.org/10.26021/3369 https://ir.canterbury.ac.nz/handle/10092/1579 unknown University of Canterbury. Chemical and Process Engineering Copyright Thomas John Hughes https://canterbury.libguides.com/rights/theses Gas Hydrates Clathrates Semi-Clathrate Dissociation DSC calorimetry CreativeWork article 2008 ftdatacite https://doi.org/10.26021/3369 2021-11-05T12:55:41Z Gas hydrates are known to form plugs in pipelines. Hydrate plug dissociation times can be predicted using the CSMPlug program. At high methane mole fractions of a methane + ethane mixture the predictions agree with experiments for the relative dissociation times of structure I (sI) and structure II (sII) plugs. At intermediate methane mole fractions the predictions disagree with experiment. Enthalpies of dissociation were measured and predicted with the Clapeyron equation. The enthalpies of dissociation for the methane + ethane hydrates were found to vary significantly with pressure, the composition, and the structure of hydrate. The prediction and experimental would likely agree if this variation in the enthalpy of dissociation was taken in to account. In doing the plug dissociation studies at high methane mole fraction a discontinuity was observed in the gas evolution rate and X-ray diffraction indicated the possibility of the presence of both sI and sII hydrate structures. A detailed analysis by step-wise modelling utilising the hydrate prediction package CSMGem showed that preferential enclathration could occur. This conclusion was supported by experiment. Salts such as tetraisopentylammonium fluoride form semi-clathrate hydrates with melting points higher than 30 ℃ and vacant cavities that can store cages such as methane and hydrogen. The stability of this semi-clathrate hydrate with methane was studied and the dissociation phase boundary was found to be at temperatures of about (25 to 30) K higher than that of methane hydrate at the same pressure. Article in Journal/Newspaper Methane hydrate DataCite Metadata Store (German National Library of Science and Technology)
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language unknown
topic Gas Hydrates
Clathrates
Semi-Clathrate
Dissociation
DSC
calorimetry
spellingShingle Gas Hydrates
Clathrates
Semi-Clathrate
Dissociation
DSC
calorimetry
Hughes, Thomas John
Plug Formation and Dissociation of Mixed Gas Hydrates and Methane Semi-Clathrate Hydrate Stability
topic_facet Gas Hydrates
Clathrates
Semi-Clathrate
Dissociation
DSC
calorimetry
description Gas hydrates are known to form plugs in pipelines. Hydrate plug dissociation times can be predicted using the CSMPlug program. At high methane mole fractions of a methane + ethane mixture the predictions agree with experiments for the relative dissociation times of structure I (sI) and structure II (sII) plugs. At intermediate methane mole fractions the predictions disagree with experiment. Enthalpies of dissociation were measured and predicted with the Clapeyron equation. The enthalpies of dissociation for the methane + ethane hydrates were found to vary significantly with pressure, the composition, and the structure of hydrate. The prediction and experimental would likely agree if this variation in the enthalpy of dissociation was taken in to account. In doing the plug dissociation studies at high methane mole fraction a discontinuity was observed in the gas evolution rate and X-ray diffraction indicated the possibility of the presence of both sI and sII hydrate structures. A detailed analysis by step-wise modelling utilising the hydrate prediction package CSMGem showed that preferential enclathration could occur. This conclusion was supported by experiment. Salts such as tetraisopentylammonium fluoride form semi-clathrate hydrates with melting points higher than 30 ℃ and vacant cavities that can store cages such as methane and hydrogen. The stability of this semi-clathrate hydrate with methane was studied and the dissociation phase boundary was found to be at temperatures of about (25 to 30) K higher than that of methane hydrate at the same pressure.
format Article in Journal/Newspaper
author Hughes, Thomas John
author_facet Hughes, Thomas John
author_sort Hughes, Thomas John
title Plug Formation and Dissociation of Mixed Gas Hydrates and Methane Semi-Clathrate Hydrate Stability
title_short Plug Formation and Dissociation of Mixed Gas Hydrates and Methane Semi-Clathrate Hydrate Stability
title_full Plug Formation and Dissociation of Mixed Gas Hydrates and Methane Semi-Clathrate Hydrate Stability
title_fullStr Plug Formation and Dissociation of Mixed Gas Hydrates and Methane Semi-Clathrate Hydrate Stability
title_full_unstemmed Plug Formation and Dissociation of Mixed Gas Hydrates and Methane Semi-Clathrate Hydrate Stability
title_sort plug formation and dissociation of mixed gas hydrates and methane semi-clathrate hydrate stability
publisher University of Canterbury. Chemical and Process Engineering
publishDate 2008
url https://dx.doi.org/10.26021/3369
https://ir.canterbury.ac.nz/handle/10092/1579
genre Methane hydrate
genre_facet Methane hydrate
op_rights Copyright Thomas John Hughes
https://canterbury.libguides.com/rights/theses
op_doi https://doi.org/10.26021/3369
_version_ 1766068864159842304