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| Content Provider | Springer Nature Link |
|---|---|
| Author | Zhu, Hai ou Kim, Jeong Rang Ihm, Son Ki |
| Copyright Year | 2009 |
| Abstract | Various Pt catalysts (Pt/ZrO$_{2}$, Pt/CeO$_{2}$, Pt/CeZrO, Pt/WO$_{3}$/ZrO$_{2}$ and Pt/WO$_{3}$/CeZrO) were prepared and characterized, and their catalytic reduction reactions of NO by CO, with or without the presence of excess oxygen, were investigated. The results of temperature-programmed experiments showed that CO could be easily oxidized over Pt/CeO$_{2}$ and Pt/CeZrO while the introduction of WO$_{3}$ into the catalyst (Pt/WO$_{3}$/CeZrO) inhibited the reduction of catalyst surface; NO could not dissociate over those catalysts in oxidized state but after CO reduction at a low temperature, NO dissociation took place only over Pt/CeO$_{2}$ and Pt/CeZrO catalysts. For NO + CO reaction, those easily reduced catalysts Pt/CeO$_{2}$ and Pt/CeZrO exhibited better catalytic performances, and NO could be rapidly converted below 350 °C. For the reaction with the presence of excess O$_{2}$, the NO conversions were significantly inhibited, but better NO conversions were obtained over the tungstate-contained catalysts when compared with Pt/CeO$_{2}$ and Pt/CeZrO. The higher activities of Pt/W–Ce–Zr catalysts were attributed to their high acidities. |
| Starting Page | 207 |
| Ending Page | 215 |
| Page Count | 9 |
| File Format | |
| ISSN | 01331736 |
| Journal | Reaction Kinetics and Catalysis Letters |
| Volume Number | 97 |
| Issue Number | 2 |
| e-ISSN | 15882837 |
| Language | English |
| Publisher | Springer Netherlands |
| Publisher Date | 2009-07-10 |
| Publisher Place | Dordrecht |
| Access Restriction | Subscribed |
| Subject Keyword | CeO$_{2}$ ZrO$_{2}$ WO$_{3}$ NO reduction CO Industrial Chemistry/Chemical Engineering Physical Chemistry Catalysis |
| Content Type | Text |
| Resource Type | Article |
| Subject | Physical and Theoretical Chemistry Catalysis |
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