|
DSpace at IIT Bombay >
IITB Publications >
Article >
Please use this identifier to cite or link to this item:
http://dspace.library.iitb.ac.in/jspui/handle/10054/7131
|
| Title: | Uranyl-anchored MCM-41 as a highly efficient photocatalyst for the complete oxidation of methanol under sunlight |
| Authors: | VIDYA, K KAMBLE, VS SELVAM, P GUPTA, NM |
| Keywords: | uranium oxide catalysts electron-transfer organic-compounds molecular-oxygen aqueous-solution mechanism ion zeolites photochemistry destruction |
| Issue Date: | 2004 |
| Publisher: | ELSEVIER SCIENCE BV |
| Citation: | APPLIED CATALYSIS B-ENVIRONMENTAL, 54(3), 145-154 |
| Abstract: | A photocatalyst that may exhibit high activity for oxidation of volatile organic compounds (VOCs) under solar radiation would offer a practical and economic means for the cleaning of air under environmental conditions. We report here for the first time that the uranyl ions anchored within the mesopores of MCM-41 may serve as an efficient heterogeneous photocatalyst for the complete destruction of methanol in vapor phase, and in the presence of sunlight and air. The uranyl-anchored MCM-41 was found to be more efficient than a TiO(2) photocatalyst in terms of CH(3)OH-->CO(2) conversion rates. The reversible and active participation of uranyl groups in the studied photocatalytic reaction was ascertained with the help of in situ fluorescence and electron paramagnetic resonance techniques, whereas the radiation-induced transient species over catalyst surface were monitored using in situ FTIR spectroscopy. The detailed reaction mechanism and the role played by uranyl ions in the photooxidation of methanol over UO(2)(2+)/MCM are elucidated on the basis of these results. (C) 2004 |
| URI: | http://dx.doi.org/10.1016/j.apcatb.2004.07.001 http://dspace.library.iitb.ac.in/xmlui/handle/10054/7131 http://hdl.handle.net/10054/7131 |
| ISSN: | 0926-3373 |
| Appears in Collections: | Article
|
Files in This Item:
There are no files associated with this item.
|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
|