Improvement of oxygen storage capacity of CeO2-ZrO2 solid solution by heat treatment in reducing atmosphere

被引:51
作者
Suda, A [1 ]
Ukyo, Y [1 ]
Sobukawa, H [1 ]
Sugiura, M [1 ]
机构
[1] Toyota Cent Res & Dev Labs Inc, Appl Catalysis Div, Nagakute, Aichi 4801192, Japan
关键词
ceria; zirconia; solid solution; reduction; oxygen storage capacity;
D O I
10.2109/jcersj.110.126
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The function of oxygen storage capacity (OSC) is very important to improve a performance for an automobile exhaust catalyst. CeO2-ZrO2 solid solution has an excellent OSC, and is available for a catalytic promoter. In this paper, OSC of the CO reduced CeO2-ZrO2 solid solution having various composition loaded with Pt was estimated by thermo gravimeter, and the phases and the crystalline structure of the reduced CeO2-ZrO2 solid solution were studied by X-ray diffraction method. The maximum total OSC-value of the reduced material occurs at the composition of 50 mol% CeO2-50 mol% ZrO2. The maximun value is about 753 mumol O-2/g-solid solution, which is about twice the value (416 mumol O-2/g-solid solution) of the attrition-milled CeO2-ZrO2 solid solution, and 5 times higher than that (150 mumol O-2/g-solid solution) of the material synthesized by conventional impregnation. The reduced material consists of Ce2Zr2O8 and CeO2 solid solution in the composition range from 30 to 50 mol% ZrO2. The reduced material consists of the mixture. Ce2Zr2O8 and ZrO2 in the composition range from 50 mol% ZrO2 to 100 mol% ZrO2. The presence of Zr4+ near Ce4+ makes the expansion easier enhancing further valence change, because Zr4+ is very small in volume. Regular distribution of Cc and Zr ions would make it possible to place Zr4+ in the nearest position to Cc ion. This would be the reason why the partial OSC of Ce2Zr2O8 is much higher than the complete solid solution.
引用
收藏
页码:126 / 130
页数:5
相关论文
共 18 条
[1]   A NOVEL AND SIMPLE ROUTE TO CATALYSTS WITH A HIGH OXYGEN STORAGE CAPACITY - THE DIRECT ROOM-TEMPERATURE SYNTHESIS OF CEO2-ZRO2 SOLID-SOLUTIONS [J].
DELEITENBURG, C ;
TROVARELLI, A ;
ZAMAR, F ;
MASCHIO, S ;
DOLCETTI, G ;
LLORCA, J .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (21) :2181-2182
[2]  
GANDHI HS, 1976, Patent No. 760201
[3]   DYNAMIC BEHAVIOR OF AUTOMOTIVE CATALYSTS .1. CATALYST OXIDATION AND REDUCTION [J].
HERZ, RK .
INDUSTRIAL & ENGINEERING CHEMISTRY PRODUCT RESEARCH AND DEVELOPMENT, 1981, 20 (03) :451-457
[4]   Crystal structure of metastable K-CeZrO4 phase possessing an ordered arrangement of Ce and Zr ions [J].
Kishimoto, H ;
Omata, T ;
Otsuka-Yao-Matsuo, S ;
Ueda, K ;
Hosono, H ;
Kawazoe, H .
JOURNAL OF ALLOYS AND COMPOUNDS, 2000, 312 (1-2) :94-103
[5]   CATALYSTS FOR AUTOMOBILE EMISSION CONTROL [J].
KUMMER, JT .
PROGRESS IN ENERGY AND COMBUSTION SCIENCE, 1980, 6 (02) :177-199
[6]   Local structure analyses of Ce0.5Zr0.5O2 mixed oxides by XAFS [J].
Nagai, Y ;
Yamamoto, T ;
Tanaka, T ;
Yoshida, S ;
Nonaka, T ;
Okamoto, T ;
Suda, A ;
Sugiura, M .
JOURNAL OF SYNCHROTRON RADIATION, 2001, 8 (08) :616-618
[7]   Vibrational spectroscopic and X-ray diffraction studies of cerium zirconium oxides with Ce/Zr composition ratio=1 prepared by reduction and successive oxidation of t′-(Ce0.5Zr0.5)O2 phase [J].
Omata, T ;
Kishimoto, H ;
Otsuka-Yao-Matsuo, S ;
Ohtori, N ;
Umesaki, N .
JOURNAL OF SOLID STATE CHEMISTRY, 1999, 147 (02) :573-583
[8]   Oxygen release behavior of CeZrO4 powders and appearance of new compounds κ and t [J].
Otsuka-Yao-Matsuo, S ;
Omata, T ;
Izu, N ;
Kishimoto, H .
JOURNAL OF SOLID STATE CHEMISTRY, 1998, 138 (01) :47-54
[9]   Oxygen evolution properties of CeO2-ZrO2 powders as automotive exhaust sub-catalysts and the phase diagrams [J].
OtsukaYao, S ;
Morikawa, H ;
Izu, N ;
Okuda, K .
JOURNAL OF THE JAPAN INSTITUTE OF METALS, 1995, 59 (12) :1237-1246
[10]   THE APPLICATION OF CE-ZR OXIDE SOLID-SOLUTION TO OXYGEN STORAGE PROMOTERS IN AUTOMOTIVE CATALYSTS [J].
OZAWA, M ;
KIMURA, M ;
ISOGAI, A .
JOURNAL OF ALLOYS AND COMPOUNDS, 1993, 193 (1-2) :73-75