The choice of precipitant and precursor in the co-precipitation synthesis of copper manganese oxide for maximizing carbon monoxide oxidation
| Autor: | Wen-Cui Li, Peter Branton, An-Hui Lu, Li-Na Cai, Yue Guo |
|---|---|
| Rok vydání: | 2012 |
| Předmět: |
Thermogravimetric analysis
Coprecipitation Process Chemistry and Technology Inorganic chemistry chemistry.chemical_element Manganese Copper manganese oxide Precipitant CO oxidation Copper Catalysis chemistry.chemical_compound Catalytic oxidation chemistry Precursor Temperature-programmed reduction Physical and Theoretical Chemistry Co-precipitation Carbon monoxide |
| Zdroj: | Journal of Molecular Catalysis A: Chemical. 360:35-41 |
| ISSN: | 1381-1169 |
| DOI: | 10.1016/j.molcata.2012.04.003 |
| Popis: | Copper manganese oxides (CMOs) were synthesized using a co-precipitation method with different precursors and precipitants for carbon monoxide oxidation. The as-synthesized catalysts were characterized by powder X-ray diffraction (XRD), low temperature N 2 sorption, Fourier transform-infrared spectroscopy (FT-IR), H 2 -temperature programmed reduction (H 2 -TPR), and thermal gravimetric analysis (TGA). Their catalytic activities for CO oxidation were tested by temperature programmed reaction. The results showed that the activity of CO oxidation strongly depended on the combination of precipitant and precursor anions, ranking in the order (Ac − + CO 3 2− ) > (NO 3 − + CO 3 2− ) > (Ac − + OH − ) > (NO 3 − + OH − ). The crystalline phase of copper manganese oxides obtained using strong electrolyte (OH − ) as the precipitant were mainly spinel Cu 1.5 Mn 1.5 O 4 , while the catalysts prepared with weak electrolyte (CO 3 2− ) as the precipitant mostly comprised of MnCO 3 , Mn 2 O 3 and CuO, and showed a much higher CO oxidation activity than that of the Cu 1.5 Mn 1.5 O 4 . Keeping the same precipitant while changing the precursor caused a change in the H 2 consumption which influenced the CO oxidation activity. A suitable combination of precipitant and precursor resulted in the most efficient CO oxidation catalyst. |
| Databáze: | OpenAIRE |
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