Effect of Pore Size Distribution on Dissociation Temperature Depression and Phase Boundary Shift of Gas Hydrate in Various Fine-Grained Sediments

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dc.contributor.authorPark, Taehyungko
dc.contributor.authorLee, Joo Yongko
dc.contributor.authorKwon, Tae-Hyukko
dc.date.accessioned2018-05-24T02:23:57Z-
dc.date.available2018-05-24T02:23:57Z-
dc.date.created2018-05-14-
dc.date.created2018-05-14-
dc.date.created2018-05-14-
dc.date.issued2018-04-
dc.identifier.citationENERGY & FUELS, v.32, no.4, pp.5321 - 5330-
dc.identifier.issn0887-0624-
dc.identifier.urihttp://hdl.handle.net/10203/242246-
dc.description.abstractCapillarity in small, confined pores has a pronounced effect on the depression of the dissociation temperature of gas hydrates, known as the Gibbs-Thomson effect. However, this effect remains poorly understood in natural fine-grained sediments with wide pore size distributions. This study investigated the effect of pore size distributions of fine-grained sediments on the dissociation temperature of a gas hydrate. A gas hydrate was synthesized under partially water-saturated conditions in nanosized silica gels and in various natural fine-grained sediment samples, including sand, silt, diatoms, a diatom-sand mixture, and clayey sediment. The synthesized hydrate samples were thermally dissociated under isochoric conditions, while the melting temperature depression and the shifted phase boundaries were monitored. We observed a dissociation temperature depression of approximately 0.1-0.3 degrees C in silt, 0.2-0.4 degrees C in the diatom sample, and 1.2-1.5 degrees C in clayey silt, while no temperature depression was observed in sand. In a particular case of diatom-sand mixture, the dual porosity condition with the submicron-scale internal pores of diatoms and the macropores of sands rendered dual phase boundaries, one with an similar to 0.4 degrees C temperature depression and one with no depression, respectively. Despite the wide ranges of pore size, gas hydrates were preferentially formed in smaller pores, which comprise less than 40% of the cumulative pore volumes. This was because the initial water loci exacerbated the Gibbs-Thomson effect in partially water-saturated conditions. Our results provide clear experimental evidence on and novel insights into the effect of pore size distributions of fine-grained sediments on the dissociation behavior and phase boundaries of gas hydrates, both in the presence of free gas and in water-limiting conditions that exhibit a considerable Gibbs-Thomson effect.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleEffect of Pore Size Distribution on Dissociation Temperature Depression and Phase Boundary Shift of Gas Hydrate in Various Fine-Grained Sediments-
dc.typeArticle-
dc.identifier.wosid000430783300130-
dc.identifier.scopusid2-s2.0-85045914478-
dc.type.rimsART-
dc.citation.volume32-
dc.citation.issue4-
dc.citation.beginningpage5321-
dc.citation.endingpage5330-
dc.citation.publicationnameENERGY & FUELS-
dc.identifier.doi10.1021/acs.energyfuels.8b00074-
dc.contributor.localauthorKwon, Tae-Hyuk-
dc.contributor.nonIdAuthorLee, Joo Yong-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusMETHANE HYDRATE-
dc.subject.keywordPlusCARBON-DIOXIDE-
dc.subject.keywordPlusSTABILITY ZONE-
dc.subject.keywordPlusCO2 HYDRATE-
dc.subject.keywordPlusMARINE-SEDIMENTS-
dc.subject.keywordPlusHEAT-TRANSFER-
dc.subject.keywordPlusPOROUS-MEDIA-
dc.subject.keywordPlusFLUID-FLOW-
dc.subject.keywordPlusWATER-
dc.subject.keywordPlusEQUILIBRIUM-
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