Natural gas recovery from hydrates in a silica sand matrix ...

This thesis studies methane hydrate crystal formation and decomposition at 1.0, 4.0 and 7.0°C in a new apparatus. Hydrate was formed in the interstitial space of a variable volume bed of silica sand particles with an average diameter equal to 329μm (150 to 630μm range). The initial pressure inside t...

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Main Author: Haligva, Cef
Format: Text
Language:English
Published: University of British Columbia 2008
Subjects:
Online Access:https://dx.doi.org/10.14288/1.0058593
https://doi.library.ubc.ca/10.14288/1.0058593
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spelling ftdatacite:10.14288/1.0058593 2023-08-27T04:10:33+02:00 Natural gas recovery from hydrates in a silica sand matrix ... Haligva, Cef 2008 https://dx.doi.org/10.14288/1.0058593 https://doi.library.ubc.ca/10.14288/1.0058593 en eng University of British Columbia Text article-journal ScholarlyArticle 2008 ftdatacite https://doi.org/10.14288/1.0058593 2023-08-07T14:24:23Z This thesis studies methane hydrate crystal formation and decomposition at 1.0, 4.0 and 7.0°C in a new apparatus. Hydrate was formed in the interstitial space of a variable volume bed of silica sand particles with an average diameter equal to 329μm (150 to 630μm range). The initial pressure inside the reactor was 8.0MPa for all the formation experiments. Three bed sizes were employed in order to observe the effects of the silica sand bed size on the rate of methane consumption (formation) and release (decomposition). The temperature at various locations inside the silica sand bed was measured with thermocouples during formation and decomposition experiments. For the decomposition experiments, two different methods were employed to dissociate the hydrate: thermal stimulation and depressurization. It was found that more than 74.0% of water conversion to hydrates was achieved in all hydrate formation experiments at 4.0°C and 1.0°C starting with a pressure of 8.0MPa. The dissociation of hydrate was found to ... Text 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 English
description This thesis studies methane hydrate crystal formation and decomposition at 1.0, 4.0 and 7.0°C in a new apparatus. Hydrate was formed in the interstitial space of a variable volume bed of silica sand particles with an average diameter equal to 329μm (150 to 630μm range). The initial pressure inside the reactor was 8.0MPa for all the formation experiments. Three bed sizes were employed in order to observe the effects of the silica sand bed size on the rate of methane consumption (formation) and release (decomposition). The temperature at various locations inside the silica sand bed was measured with thermocouples during formation and decomposition experiments. For the decomposition experiments, two different methods were employed to dissociate the hydrate: thermal stimulation and depressurization. It was found that more than 74.0% of water conversion to hydrates was achieved in all hydrate formation experiments at 4.0°C and 1.0°C starting with a pressure of 8.0MPa. The dissociation of hydrate was found to ...
format Text
author Haligva, Cef
spellingShingle Haligva, Cef
Natural gas recovery from hydrates in a silica sand matrix ...
author_facet Haligva, Cef
author_sort Haligva, Cef
title Natural gas recovery from hydrates in a silica sand matrix ...
title_short Natural gas recovery from hydrates in a silica sand matrix ...
title_full Natural gas recovery from hydrates in a silica sand matrix ...
title_fullStr Natural gas recovery from hydrates in a silica sand matrix ...
title_full_unstemmed Natural gas recovery from hydrates in a silica sand matrix ...
title_sort natural gas recovery from hydrates in a silica sand matrix ...
publisher University of British Columbia
publishDate 2008
url https://dx.doi.org/10.14288/1.0058593
https://doi.library.ubc.ca/10.14288/1.0058593
genre Methane hydrate
genre_facet Methane hydrate
op_doi https://doi.org/10.14288/1.0058593
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