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dc.contributor.authorLin, Liang-Yien_US
dc.contributor.authorBai, Hsunlingen_US
dc.date.accessioned2019-04-03T06:42:16Z-
dc.date.available2019-04-03T06:42:16Z-
dc.date.issued2016-01-01en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c5ra27488een_US
dc.identifier.urihttp://hdl.handle.net/11536/133571-
dc.description.abstractHollow and mesoporous CoOx/SiO2 spheres (denoted as CoOx/hSiO(2) and CoOx/mSiO(2)) were synthesized via salt-assisted ultrasonic spray pyrolysis. Precursor solutions containing sodium silicate solution, a mineral acid (hydrochloric acid or nitric acid) and a cobalt salt were ultrasonically aerosolized and pyrolyzed. Results showed that CoOx/SiO2 spheres with hollow or mesoporous structure can be fabricated by using the NaCl and NaNO3 salts as in situ formed templates. Significantly, this approach avoids the need for post-calcination for template elimination, instead permitting aqueous removal with water. The influence of the sodium salts on the characteristics of CoOx/SiO2 spheres was investigated by means of XRD, nitrogen physisorption, SEM/TEM, ICP-MS, UV-Vis, XPS and H-2-TPR. On the basis of the experimental results, a possible mechanism on the formation of hollow and mesoporous spheres was proposed. The CoOx/SiO2 spheres were tested as catalysts for toluene oxidation. The mesoporous CoOx/mSiO(2) was found to exhibit superior activity to hollow CoOx/hSiO(2), probably attributed to a combination of several factors, including the predominant existence of a Co3O4 active phase, high surface Co3+ content, and easy reducibility of Co3+ at low temperature.en_US
dc.language.isoen_USen_US
dc.titleSalt-induced formation of hollow and mesoporous CoOx/SiO2 spheres and their catalytic behavior in toluene oxidationen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c5ra27488een_US
dc.identifier.journalRSC ADVANCESen_US
dc.citation.volume6en_US
dc.citation.issue29en_US
dc.citation.spage24304en_US
dc.citation.epage24313en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000372256800039en_US
dc.citation.woscount5en_US
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