A HIGH YIELD PROCESS FOR HYDRATE FORMATION ...

A new procedure was studied to obtain concentrated methane hydrates in bulk, at medium-low pressure, avoiding the use of the spray process. Methane hydrate was formed at about 5 MPa and 2 °C in a reaction calorimeter with the volume of two liters. The clathrate concentration was about 30% and the fi...

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Main Authors: Giavarini, Carlo, Maccioni, Filippo
Format: Text
Language:English
Published: The University of British Columbia 2008
Subjects:
Online Access:https://dx.doi.org/10.14288/1.0041126
https://doi.library.ubc.ca/10.14288/1.0041126
id ftdatacite:10.14288/1.0041126
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spelling ftdatacite:10.14288/1.0041126 2024-04-28T08:28:22+00:00 A HIGH YIELD PROCESS FOR HYDRATE FORMATION ... Giavarini, Carlo Maccioni, Filippo 2008 https://dx.doi.org/10.14288/1.0041126 https://doi.library.ubc.ca/10.14288/1.0041126 en eng The University of British Columbia article-journal Text ScholarlyArticle 2008 ftdatacite https://doi.org/10.14288/1.0041126 2024-04-02T09:56:45Z A new procedure was studied to obtain concentrated methane hydrates in bulk, at medium-low pressure, avoiding the use of the spray process. Methane hydrate was formed at about 5 MPa and 2 °C in a reaction calorimeter with the volume of two liters. The clathrate concentration was about 30% and the final reactor pressure was 2.7 MPa. Any further repressurization at 2 °C had no noticeable effect on the hydrate formation. However, by repressurizing the vessel again to 4 MPa and increasing the temperature near the decomposition value (about 6° C) more clathrate was formed. Repressurizing again the reactor at 4 MPa and controlling the temperature at the same level, a concentration of 88% hydrate in the bulk was reached. Respect to the hydrate produced by the spray process, this procedure takes more time, but it can be sped up and made continuous by using teo reaction vessels, one for hydrate formation and the other for hydrate concentration. The advantage is the production of concentrated hydrates, by a simple ... 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)
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language English
description A new procedure was studied to obtain concentrated methane hydrates in bulk, at medium-low pressure, avoiding the use of the spray process. Methane hydrate was formed at about 5 MPa and 2 °C in a reaction calorimeter with the volume of two liters. The clathrate concentration was about 30% and the final reactor pressure was 2.7 MPa. Any further repressurization at 2 °C had no noticeable effect on the hydrate formation. However, by repressurizing the vessel again to 4 MPa and increasing the temperature near the decomposition value (about 6° C) more clathrate was formed. Repressurizing again the reactor at 4 MPa and controlling the temperature at the same level, a concentration of 88% hydrate in the bulk was reached. Respect to the hydrate produced by the spray process, this procedure takes more time, but it can be sped up and made continuous by using teo reaction vessels, one for hydrate formation and the other for hydrate concentration. The advantage is the production of concentrated hydrates, by a simple ...
format Text
author Giavarini, Carlo
Maccioni, Filippo
spellingShingle Giavarini, Carlo
Maccioni, Filippo
A HIGH YIELD PROCESS FOR HYDRATE FORMATION ...
author_facet Giavarini, Carlo
Maccioni, Filippo
author_sort Giavarini, Carlo
title A HIGH YIELD PROCESS FOR HYDRATE FORMATION ...
title_short A HIGH YIELD PROCESS FOR HYDRATE FORMATION ...
title_full A HIGH YIELD PROCESS FOR HYDRATE FORMATION ...
title_fullStr A HIGH YIELD PROCESS FOR HYDRATE FORMATION ...
title_full_unstemmed A HIGH YIELD PROCESS FOR HYDRATE FORMATION ...
title_sort high yield process for hydrate formation ...
publisher The University of British Columbia
publishDate 2008
url https://dx.doi.org/10.14288/1.0041126
https://doi.library.ubc.ca/10.14288/1.0041126
genre Methane hydrate
genre_facet Methane hydrate
op_doi https://doi.org/10.14288/1.0041126
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