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An ethylenediamine-grafted Y zeolite: a highly regenerable carbon dioxide adsorbent via temperature swing adsorption without urea formation

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dc.contributor.authorKim, Chaehoon-
dc.contributor.authorCho, Hae Sung-
dc.contributor.authorChang, Shuai-
dc.contributor.authorCho, Sung June-
dc.contributor.authorChoi, Minkee-
dc.date.accessioned2023-03-08T17:37:59Z-
dc.date.available2023-03-08T17:37:59Z-
dc.date.issued2016-05-
dc.identifier.issn1754-5692-
dc.identifier.issn1754-5706-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/64243-
dc.description.abstractSolid adsorbents including amine-functionalized porous materials and zeolites have been extensively investigated for post-combustion CO2 capture. Amine-functionalized porous materials have shown highly promising CO2 uptake in a wet flue gas, but suffer from significant amine deactivation due to urea formation under desorption conditions (e.g., desorption under 100% CO2 at >130 degrees C) of temperature swing adsorption (TSA) cycles. In contrast, purely inorganic zeolites are thermochemically stable but cannot adsorb CO2 from a wet flue gas because of the preferential H2O adsorption. In the present work, we synthesized an ethylenediamine-grafted Y zeolite, which can synergistically combine the strengths of both adsorbent systems. The amine groups can effectively capture CO2 in a wet flue gas, while the strongly co-adsorbed H2O within the hydrophilic zeolite micropores suppresses urea formation (dehydration reaction between amines and CO2) under desorption conditions according to Le Chatelier's principle. The organic-zeolite hybrid adsorbent retains working capacities higher than 1.1 mmol g(-1) over 20 TSA cycles. Because the adsorbent is prepared from a commercially available zeolite, it is also highly cost efficient and suitable for mass production.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleAn ethylenediamine-grafted Y zeolite: a highly regenerable carbon dioxide adsorbent via temperature swing adsorption without urea formation-
dc.typeArticle-
dc.identifier.doi10.1039/c6ee00601a-
dc.identifier.bibliographicCitationENERGY & ENVIRONMENTAL SCIENCE, v.9, no.5, pp 1803 - 1811-
dc.description.isOpenAccessN-
dc.identifier.wosid000375699500024-
dc.identifier.scopusid2-s2.0-84970983741-
dc.citation.endPage1811-
dc.citation.number5-
dc.citation.startPage1803-
dc.citation.titleENERGY & ENVIRONMENTAL SCIENCE-
dc.citation.volume9-
dc.type.docTypeArticle-
dc.publisher.location영국-
dc.subject.keywordPlusMETAL-ORGANIC FRAMEWORKS-
dc.subject.keywordPlusMESOPOROUS MOLECULAR-SIEVE-
dc.subject.keywordPlusCO2 CAPTURE-
dc.subject.keywordPlusCO2-INDUCED DEGRADATION-
dc.subject.keywordPlusSOLID ADSORBENTS-
dc.subject.keywordPlusHIGH-CAPACITY-
dc.subject.keywordPlusFLUE-GAS-
dc.subject.keywordPlusSILICA-
dc.subject.keywordPlusSORBENTS-
dc.subject.keywordPlusAMINES-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEnergy & Fuels-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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