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dc.contributor.authorWu, Chih-Hsiangen_US
dc.contributor.authorChang, Yen-Poen_US
dc.contributor.authorChen, San-Yuanen_US
dc.contributor.authorLiu, Dean-Moen_US
dc.contributor.authorYu, Ching-Tsungen_US
dc.contributor.authorPen, Ben-Lien_US
dc.date.accessioned2019-04-02T05:59:35Z-
dc.date.available2019-04-02T05:59:35Z-
dc.date.issued2010-07-01en_US
dc.identifier.issn1533-4880en_US
dc.identifier.urihttp://dx.doi.org/10.1166/jnn.2010.1708en_US
dc.identifier.urihttp://hdl.handle.net/11536/149940-
dc.description.abstractIn this work, monodispersed layered double hydroxide (Ca-Al LDHs) nanoparticles were synthesized by hydrothermal coprecipitation. Uniform thin films of layered double hydroxide on porous anodic aluminum oxide (AAO) substrates were formed by a direct precipitation process in a homogeneous suspension containing monodispersed Ca-Al layered double hydroxide nanoparticles. It was found that the formation of a designed hydrotalcite-like phase is strongly dependent on the [Ca2-]/ [Al3+] ratios, and that a minor CaCO3 phase could possibly form simultaneously, which is attributed to the greater insolubility of CaCO3 and the incompatibility of the ionic size of Al and Ca. The optimal CO2 adsorption capacity appears in the layered Ca-OH-Al structure with the composition ratio of 3:1. Furthermore, the CO2 adsorption mechanism varies with treatment temperature. Below 400 degrees C, the CO2 adsorption is attributed to the LDH structure with a large surface area and pore volume, but above that the adsorption is due to the formation of CaCO3 and CaO. The permeation behavior and CO2 absorption can be explained by a preferable chemical and physical absorption of CO2 on the layered double hydroxide and porous structure of the membrane.en_US
dc.language.isoen_USen_US
dc.subjectLayered Double Hydroxideen_US
dc.subjectNanoparticleen_US
dc.subjectCO2 Absorptionen_US
dc.subjectMembraneen_US
dc.subjectAnodic Aluminum Oxideen_US
dc.titleCharacterization and Structure Evolution of Ca-Al-CO3 Hydrotalcite Film for High Temperature CO2 Adsorptionen_US
dc.typeArticleen_US
dc.identifier.doi10.1166/jnn.2010.1708en_US
dc.identifier.journalJOURNAL OF NANOSCIENCE AND NANOTECHNOLOGYen_US
dc.citation.volume10en_US
dc.citation.spage4716en_US
dc.citation.epage4720en_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:000277199300098en_US
dc.citation.woscount15en_US
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