CuO;
Solid solution of copper in ceria;
Total oxidation;
VOCs;
Carbon monoxide;
In situ XRD;
EXAFS modeling;
X-RAY-ABSORPTION;
VOLATILE ORGANIC-COMPOUNDS;
COPPER-OXIDE CATALYSTS;
CO OXIDATION;
CARBON-MONOXIDE;
ETHYL-ACETATE;
MIXED-OXIDE;
F-TEST;
REDUCTION;
SPECTROSCOPY;
D O I:
10.1007/s10562-013-1144-x
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Different types of copper oxide in CuO-CeO2/Al2O3 were investigated structurally and catalytically. Standard preparation lead to the presence of CuO monocrystals and Ce1-xCuxO2-x as evidenced by XRD, HRTEM and EDX. Washing with nitric acid removed the monocrystals, while leaving the Ce1-xCuxO2-x solid solution. The Fourier transformed Cu K patterns for the HNO3-washed catalyst showed a diminished second Cu shell, characteristic for Ce1-xCuxO2-x as well as for X-ray amorphous nano-sized CuAl2O4 spinel phase. XANES analysis and first shell Cu fitting confirmed this CuAl2O4 like structure outside Ce1-xCuxO2-x. By modeling the Ce K EXAFS signal in the washed sample, the amount of Cu in Ce1-xCuxO2-x was determined to be 18 +/- 6 %. Total oxidation of CO and C3H8 as model reactions showed little difference in activity between non-washed and washed CuO-CeO2/Al2O3, indicating that CuO monocrystals were hardly active at temperatures below 450 degrees C. XRD performed in situ during TPR and TPO showed that CeO2 in Ce1-xCuxO2-x added to the redox capacity of both CuO-CeO2/Al2O3 samples as it was partially reduced at 300 degrees C. At higher temperatures, the CuO monocrystals also participated in reaction, leading to a higher activity for the oxidation of CH4.