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dc.contributor.authorWeng, Sheng-Fengen_US
dc.contributor.authorWang, Yun-Hsinen_US
dc.contributor.authorLee, Chi-Shenen_US
dc.date.accessioned2014-12-08T15:30:12Z-
dc.date.available2014-12-08T15:30:12Z-
dc.date.issued2013-05-02en_US
dc.identifier.issn0926-3373en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.apcatb.2013.01.025en_US
dc.identifier.urihttp://hdl.handle.net/11536/21644-
dc.description.abstractPyrochlore phases solid solutions, La2Ce2-xRuxO7 (x=0-0.35) were prepared with a sol-gel process and used as catalysts for the autothermal steam reforming of ethanol. The samples as prepared were characterized with powder X-ray diffraction (PXRD), X-ray photoelectron spectra (XPS), and temperature-programmed reduction (TPR). The XPS and TPR spectra revealed the effect of doped Run+ to oxidation states of La and Ce sites. The low temperature reduction ability and relative concentration of Ce4+ ions are increased as the cell-dimension decreased. Tests of catalytic activity showed that the reforming performance of La2Ce2-xRuxO7 catalysts was affected by the Ru/Ce loading ratio. For all catalysts, partial oxidation was favored at a large C/O composition; incomplete ethanol conversion was observed for C/O >= 0.7. The optimized catalyst was La2Ce1.8Ru0.2O7 with hydrogen production rate (r(H2)) 2.01 x 10(-3) mol s(-1) g(cat)(-1) (autothermal temperature similar to 600 degrees C and 97% ethanol conversion at C/O=0.6). The catalyst exhibited stable r(H2) over 26 h of the reaction with ethanol conversion >95%. r(H2) of the catalyst gradually decreased thereafter because LaAlO3 started to formed and affected catalytic process. For the catalyst, the Ru ions remained well dispersed before and after the AESR reaction. (C) 2013 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectAutothermal steam reforming of ethanolen_US
dc.subjectPyrochloreen_US
dc.subjectSolid solutionen_US
dc.subjectRutheniumen_US
dc.titleAutothermal steam reforming of ethanol over La2Ce2-xRuxO7 (x=0-0.35) catalyst for hydrogen productionen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.apcatb.2013.01.025en_US
dc.identifier.journalAPPLIED CATALYSIS B-ENVIRONMENTALen_US
dc.citation.volume134en_US
dc.citation.issueen_US
dc.citation.spage359en_US
dc.citation.epage366en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000316583500042-
dc.citation.woscount5-
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