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Seo, Yongwon
Advanced Clean Energy Lab.
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dc.citation.endPage 18929 -
dc.citation.number 19 -
dc.citation.startPage 18918 -
dc.citation.title ENERGY & FUELS -
dc.citation.volume 38 -
dc.contributor.author Go, Woojin -
dc.contributor.author Jung, Jongyeon -
dc.contributor.author Park, Myungchul -
dc.contributor.author Sohn, Young Hoon -
dc.contributor.author Lim, Junkyu -
dc.contributor.author Seo, Yongwon -
dc.contributor.author Seo, Yutaek -
dc.date.accessioned 2024-10-10T13:35:08Z -
dc.date.available 2024-10-10T13:35:08Z -
dc.date.created 2024-10-08 -
dc.date.issued 2024-09 -
dc.description.abstract The quest for environmentally sustainable solutions for CO2 recovery and purification has led to the development of innovative separation techniques, which are crucial for carbon capture, utilization, and storage (CCUS) applications. Moreover, refrigerant recovery techniques have been widely developed after the implementation of stringent global regulations on hydrofluorocarbon (HFC) emissions. This study explores the separation of R134a, a well-known HFC, from carbon dioxide (CO2), focusing on the feasibility of hydrate-based processes for the recovery of high-purity CO2. Phase equilibrium measurements, spectroscopic analysis, and process simulation studies were systematically performed to evaluate the operation conditions and energy requirements of the hydrate-based separation processes. Phase equilibrium measurements for R134a + CO2 mixtures at various concentrations were performed along with the structural analysis of mixed hydrates using low-temperature powder X-ray diffraction (PXRD). The experiments demonstrated the preferential occupation of R134a into hydrate cages, enriching CO2 in the vapor phase and achieving target purity levels of 99.0 mol % CO2. The PXRD patterns confirmed the formation of structure II hydrates with a lattice parameter of 17.2 & Aring; with inclusions of R134a in large cages, resulting in a higher exothermic heat of formation compared with that of structure I hydrates. Process simulations were performed to further extend these findings, highlighting the favorable operation conditions and the exothermic nature of hydrate formation, which suggested heat integration into other process units. This study represents a pioneering effort in modeling hydrate-based CO2 recovery processes, providing a significant contribution to the development of sustainable industrial practices and the advancement of CCUS technologies. -
dc.identifier.bibliographicCitation ENERGY & FUELS, v.38, no.19, pp.18918 - 18929 -
dc.identifier.doi 10.1021/acs.energyfuels.4c03766 -
dc.identifier.issn 0887-0624 -
dc.identifier.scopusid 2-s2.0-85205927869 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/84034 -
dc.identifier.wosid 001318663800001 -
dc.language 영어 -
dc.publisher AMER CHEMICAL SOC -
dc.title Advancing the Hydrate-Based CO2 Separation Process by Implementing Spectroscopic Analysis and Process Simulation -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Energy & Fuels; Engineering, Chemical -
dc.relation.journalResearchArea Energy & Fuels; Engineering -
dc.type.docType Article; Early Access -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus CARBON-DIOXIDE -
dc.subject.keywordPlus FLUE-GAS -
dc.subject.keywordPlus HFC-134A -
dc.subject.keywordPlus CAPTURE -
dc.subject.keywordPlus SYSTEMS -
dc.subject.keywordPlus EQUILIBRIUM -
dc.subject.keywordPlus GAS-MIXTURES -
dc.subject.keywordPlus DISSOCIATION ENTHALPIES -

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