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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/49968


    Title: Removal of CO in excess hydrogen over CuO/Ce(1-x)Mn(x)O(2) catalysts
    Authors: Peng,CT;Lia,HK;Liaw,BJ;Chen,YZ
    Contributors: 化學工程與材料工程學系
    Keywords: CARBON-MONOXIDE OXIDATION;COPPER-CERIA CATALYSTS;FUEL-CELL APPLICATIONS;MIXED-OXIDE CATALYSTS;SELECTIVE OXIDATION;PREFERENTIAL OXIDATION;CUO-CEO2 CATALYST;REDOX PROPERTIES;SOLID-SOLUTIONS;BEHAVIOR
    Date: 2011
    Issue Date: 2012-03-27 16:27:39 (UTC+8)
    Publisher: 國立中央大學
    Abstract: Ce(1-x)Mn(x)O(2) mixed oxides were used as supports for preparing 7%CuO/Ce(1-x)Mn(x)O(2) catalysts by impregnation for the preferential oxidation (PROX) of CO in excess hydrogen. Incorporating an appropriate amount of manganese into CeO(2) to form Ce(1-x)Mn(x)O(2) solution increased the mobility of lattice oxygen and improved performance of CuO/Ce(1-x)Mn(x)O(2) catalysts in the PROX of CO. CO oxidation proceeded at the interfacial perimeter through an interaction between CuO clusters and Ce(1-x)Mn(x)O(2), involving not only the redox behavior of CeO(2) but also that of MnO(x). The PROX reaction was not weakened as the fraction of manganese incorporated in the 7%CuO/Ce(1-x)Mn(x)O(2) catalysts increased up to 0.3. A small amount of doped Me and an appropriate amount of incorporated Al(2)O(3) could obtain a good candidate such as 7%CuO/Ce(0.9)Mn(0.1)O(2)-20%Al(2)O(3) for a PROX unit in a polymer electrolyte membrane fuel cell system for removing CO. Its activity was comparable with, and its selectivity was much larger than, that of the noble catalyst 5%Pt/Al(2)O(3). (C) 2011 Elsevier B.V. All rights reserved.
    Relation: CHEMICAL ENGINEERING JOURNAL
    Appears in Collections:[Department of Chemical and Materials Engineering] journal & Dissertation

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