High Resolution Image Download MS PowerPoint Slide Catalytic oxidation of CO over Ce x Hf 1 - x O 2 (CH; 8:2 mole ratio) and Ce x Zr 1 - x O 2 (CZ; 1:1 mole ratio) nanocomposite oxides reveals that the former combination exhibits more conversion at much lower temperature than the latter. Thermal and textural stability of both the combinations, obtained by a coprecipitation method and calcined at 773 and 1073 K, were examined by X-ray diffraction, Raman spectroscopy, and CO-temperature programmed reduction techniques. The XRD results disclose formation of a stable Ce 0.8 Hf 0.2 O 2 cubic phase in the case of the CH sample, whereas CZ suffers phase segregation from Ce 0.75 Zr 0.25 O 2 to Ce 0.6 Zr 0.4 O 2 at 1073 K. Oxygen storage capacity (OSC) and CO-TPR measurements reveal a high OSC and low-temperature reducibility for the CH sample due to the defective fluorite structure generated upon incorporation of smaller Hf 4+ cations (0.78 Å ionic radius), in comparison to Zr 4+ (0.84 Å), into the ceria cubic lattice. The observed high activity of Ce 0.8 Hf 0.2 O 2 was proven to be due to the generation of lattice defects, formation of more oxygen vacancies, and easy reducibility.
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Reddy et al. (2007) studied this question.
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