完整後設資料紀錄
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dc.contributor.authorChang, Po-hsuehen_US
dc.contributor.authorHuang, Wei-Chenen_US
dc.contributor.authorLee, Tai-Jungen_US
dc.contributor.authorChang, Yen-Poen_US
dc.contributor.authorChen, San-Yuanen_US
dc.date.accessioned2015-07-21T08:29:28Z-
dc.date.available2015-07-21T08:29:28Z-
dc.date.issued2015-03-25en_US
dc.identifier.issn1944-8244en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acsami.5b00033en_US
dc.identifier.urihttp://hdl.handle.net/11536/124495-
dc.description.abstractIn this study, highly efficient high-temperature CO2 sorbents of calcium aluminate (Ca-Al-O) mesostructured composite were synthesized using presynthesized mesoporous alumina (MA) as a porous matrix to react with calcium nitrate through a microwave-assisted process. Upon annealing at 600 degrees C, a highly stable mesoporous structure composed of poorly crystalline Ca(12)A(14)O(33) phase and the CaO matrix was obtained. The Ca-Al-O mesostructured sorbents with a Ca2+/Al3+ ratio of 5:1 exhibit an enhanced increasing CO2 absorption kinetics in the CO2 capture capacity from 37.2 wt % to 48.3 wt % without apparent degradation With increasing carbonation/calcination cycling up to 50 at 700 degrees C due to the strong self-reactivation effect of the mesoporous Ca-Al-O microstructure. Remarkable improvements in the CaO-CaCO3 conversion attained from the mesostructured Ca-Al-O composite can be explained using the concept combined with available mesoporous structure and Ca12Al14O33 phase content. However, a high Ca2+/Al3+ =8:1 Ca-Al-O composite causes degradation because the pores become blocked and partial sintering induces CaO agglomeration.en_US
dc.language.isoen_USen_US
dc.subjectCa-Al-O mesoporousen_US
dc.subjectcarbon dioxide captureen_US
dc.subjectcarbonation/calcinationen_US
dc.subjectmicrowave-assisteden_US
dc.titleSelf-Reactivated Mesostructured Ca-Al-O Composite for Enhanced High-Temperature CO2 Capture and Carbonation/Calcination Cycles Performanceen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acsami.5b00033en_US
dc.identifier.journalACS APPLIED MATERIALS & INTERFACESen_US
dc.citation.issue11en_US
dc.citation.spage6172en_US
dc.citation.epage6179en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000351972400022en_US
dc.citation.woscount0en_US
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