Abstract
Au supported on γ-Al2O3 prepared by deposition-precipitation (DP) using urea is found to be a highly active catalyst for the total oxidation of HCHO at room temperature under humid air, without the need for a reducible oxide as support. In-situ DRIFTS studies suggested that the surface hydroxyl groups played a key role in the partial oxidation of HCHO into the formate intermediates, which can be further oxidized into CO 2 and H2O with participation of nano-Au. This study challenges the traditional idea of supporting noble metals on reducible oxides for HCHO oxidation at room temperature.
Original language | English |
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Pages (from-to) | 93-97 |
Number of pages | 5 |
Journal | Catalysis Communications |
Volume | 42 |
DOIs | |
State | Published - 2013 |
Bibliographical note
Funding Information:The work was supported by the National Natural Foundation of China (Nos. 21373037 and 21073024 ), Natural Science Foundation of Liaoning Province (No. 201102034 ) and by the Program for New Century Excellent Talents in University ( NCET-07-0136 ), as well as by the Fundamental Research Funds for the Central Universities (No. DUT12LK23 ).
Funding
The work was supported by the National Natural Foundation of China (Nos. 21373037 and 21073024 ), Natural Science Foundation of Liaoning Province (No. 201102034 ) and by the Program for New Century Excellent Talents in University ( NCET-07-0136 ), as well as by the Fundamental Research Funds for the Central Universities (No. DUT12LK23 ).
Funders | Funder number |
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National Natural Science Foundation of China (NSFC) | 21073024, 21373037 |
Program for New Century Excellent Talents in University | NCET-07-0136 |
Natural Science Foundation of Liaoning Province | 201102034 |
Fundamental Research Funds for the Central Universities |
Keywords
- Au/γ-AlO
- Catalytic oxidation
- Formaldehyde
- Room temperature
ASJC Scopus subject areas
- Catalysis
- General Chemistry
- Process Chemistry and Technology