File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

서용원

Seo, Yongwon
Advanced Clean Energy Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 239 -
dc.citation.startPage 229 -
dc.citation.title APPLIED ENERGY -
dc.citation.volume 228 -
dc.contributor.author Lee, Yohan -
dc.contributor.author Choi, Wonjung -
dc.contributor.author Seo, Young-ju -
dc.contributor.author Lee, Joo Yong -
dc.contributor.author Lee, Jaehyoung -
dc.contributor.author Seo, Yongwon -
dc.date.accessioned 2023-12-21T20:09:09Z -
dc.date.available 2023-12-21T20:09:09Z -
dc.date.created 2018-11-06 -
dc.date.issued 2018-10 -
dc.description.abstract This study investigated a structural transition induced by cage-dependent guest exchange in the CH4 + C3H8 hydrate with CO2 injection for CH4 recovery and CO2 sequestration. The influence of the CO2 replacement on the crystalline structure of initial CH4 + C3H8 hydrates and the cage-dependent distribution of guest molecules were quantitatively investigated using powder X-ray diffraction, C-13 nuclear magnetic resonance spectroscopy, and gas chromatography. The quantitative analyses demonstrated that the CO2 occupation caused the depletion of C3H8 molecules in the large 5(12)6(4) cages of structure II hydrates, thereby resulting in the subsequent transformation into CO2-rich sI hydrates and the coexistence of structure I and structure II hydrates after the replacement. The guest-exchange behavior observed from time-dependent Raman spectra indicated that the replacement rate was increased with an increase in pressure of injected CO2 and that the extent of the replacement was enhanced at higher pressure of injected CO2. Overall experimental evidence of the partial structural-transition replacement suggests that CO2 molecules first occupied structure II hydrates predominantly with the rapid guest exchange at the surface and that the initial structure II hydrates were subsequently converted to the CO2-rich structure I hydrates from the surface to the inner side. Precise identification of the mechanism responsible for the partial structural transition occurring in the CH4 + C3H8- CO2 replacement will be very helpful in developing a strategy for actual CO2 injection into structure II gas hydrate reservoirs for energy recovery and CO2 sequestration. -
dc.identifier.bibliographicCitation APPLIED ENERGY, v.228, pp.229 - 239 -
dc.identifier.doi 10.1016/j.apenergy.2018.06.088 -
dc.identifier.issn 0306-2619 -
dc.identifier.scopusid 2-s2.0-85048862486 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/25092 -
dc.identifier.url https://www.sciencedirect.com/science/article/pii/S0306261918309590?via%3Dihub -
dc.identifier.wosid 000447479400020 -
dc.language 영어 -
dc.publisher ELSEVIER SCI LTD -
dc.title Structural transition induced by cage-dependent guest exchange in CH4 + C3H8 hydrates with CO2 injection for energy recovery and CO2 sequestration -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Energy & Fuels; Engineering, Chemical -
dc.relation.journalResearchArea Energy & Fuels; Engineering -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Gas hydrate -
dc.subject.keywordAuthor Replacement -
dc.subject.keywordAuthor CO2 sequestration -
dc.subject.keywordAuthor Structure II -
dc.subject.keywordAuthor Strucutral transition -
dc.subject.keywordPlus CARBON DIOXIDE REPLACEMENT -
dc.subject.keywordPlus GAS HYDRATE FORMATION -
dc.subject.keywordPlus METHANE HYDRATE -
dc.subject.keywordPlus THERMAL-STIMULATION -
dc.subject.keywordPlus C-13 NMR -
dc.subject.keywordPlus FLUE-GAS -
dc.subject.keywordPlus CO2 -
dc.subject.keywordPlus RECOVERY -
dc.subject.keywordPlus WATER -
dc.subject.keywordPlus SII -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.