Modification of CeO2 on the redox property of Fe2O3

被引:50
作者
Li, Kongzhai [1 ,2 ]
Haneda, Masaaki [1 ]
Gu, Zhenhua [3 ]
Wang, Hua [2 ]
Ozawa, Masakuni [1 ]
机构
[1] Nagoya Inst Technol, Dept Frontier Mat, Adv Ceram Res Ctr, Tajimi, Gifu 5070071, Japan
[2] Kunming Univ Sci & Technol, Minist Educ, Engn Res Ctr Met Energy Conservat & Emiss Reduct, Kunming 650093, Yunnan, Peoples R China
[3] Kunming Univ Sci & Technol, Oxbridge Coll, Kunming 650106, Yunnan, Peoples R China
关键词
CeO2; Fe2O3; Oxygen storage capacity; Redox; CeFeO3; IRON-OXIDES; FUEL-CELL; PARTIAL OXIDATION; HYDROGEN STORAGE; NITROGEN-OXIDES; SURFACE-AREA; METHANE; CATALYSTS; OXYGEN; REDUCTION;
D O I
10.1016/j.matlet.2012.09.039
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The modifications of CeO2 on the reduction behavior, oxygen storage capacity (OSC), and redox stability of Fe2O3 were investigated. Combination of Fe2O3 with CeO2 strongly improved the low-temperature reducibility of both Fe2O3 and CeO2, evidencing an obvious interaction between cerium and iron oxides during the H-2-TPR process. Most of the Fe3+ in single Fe2O3 cannot be restored by the re-oxidation step (OSC step) after the TPR testing, which resulted in a serious decrease in the OSC. On the other hand, the presence of CeO2 significantly enhanced the redox property of Fe2O3: more iron (III) ions were observed in the recycled CeO2/Fe2O3 mixture (Ce/Fe=1/4, labeled Ce20Fe80 sample), and the OSC was obviously improved by the redox treatment. After the first TPR/OSC cycle, the reduction behavior of the recycled Ce20Fe80 sample is highly reversible, indicating good redox stability. This is attributed to the formation of perovskite-type CeFeO3 with excess CeO2, Fe2O3 and Fe in the recycled Ce20Fe80 sample. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 132
页数:4
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