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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Aboukaïs, Antoine Bechara, Rafeh Bonnelle, Jean-Pierre |
| Copyright Year | 1993 |
| Abstract | The surface changes of a Cu–Al–O catalyst under H2 or CO atmospheres have been followed by X-ray photoelectron spectroscopy (XPS). In both cases, the progressive reduction of copper(II) species in the octahedral and tetrahedral sites to lower oxidation states for temperatures above 250 °C is observed. When the catalyst is reduced by H2, the main Cu 2p3/2 peak is resolved into its components (Cu2+, Cu+ in tetrahedral and octahedral sites, Cu0) and the proportion of the different copper species has been calculated. The concentration of Cu+ species in the octahedral environment is maximum after reducing the catalyst at 300 °C, which corresponds to better catalytic activity in the hydrogenation of dienes. In case of Cu–Al–O treated by CO where the catalyst surface contained copper species with oxidation states lower than +2, the adsorption of carbon monoxide in a molecular state seems more probable than dissociation which leads to carbidic species. |
| Starting Page | 1257 |
| Ending Page | 1262 |
| Page Count | 6 |
| File Format | |
| ISSN | 09565000 |
| Volume Number | 89 |
| Issue Number | 8 |
| Journal | Journal of the Chemical Society, Faraday Transactions |
| DOI | 10.1039/FT9938901257 |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Cu Adsorption Photoemission spectroscopy Carbon monoxide Dissociative Copper Hydrogenation X-ray photoelectron spectroscopy |
| Content Type | Text |
| Resource Type | Article |
| Subject | Physical and Theoretical Chemistry |
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