Vapor phase nitration of benzene using mesoporous MoO3/SiO2 solid acid catalyst
| Autor: | S. B. Shelke, S. P. Dagde, Pratap T Patil, Sanyo M. Mathew, Mohan K. Dongare, Shubhangi B. Umbarkar, Kusum M Malshe, S. P. Niphadkar, Ankush V. Biradar |
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| Rok vydání: | 2006 |
| Předmět: | |
| Zdroj: | Green Chemistry. 8:488 |
| ISSN: | 1463-9270 1463-9262 |
| DOI: | 10.1039/b600094k |
| Popis: | Nitration of benzene has been carried out in the vapor phase, using dilute nitric acid as the nitrating agent, over mesoporous MoO3/SiO2 solid acid catalyst with more than 90% benzene conversion and 99.9% selectivity for mononitrobenzene. A series of MoO3/SiO2 catalysts with varying MoO3 loadings (1–30 mol%) were prepared using a sol–gel technique and characterized using X-ray diffraction analysis (XRD), BET specific surface area analysis, temperature-programmed desorption (TPD) of ammonia, and FTIR spectroscopic analysis of adsorbed pyridine. XRD analysis revealed the amorphous nature of the catalyst for 1 and 10 mol% MoO3 loading, and the formation of a crystalline α-MoO3 phase on the amorphous silica support at higher MoO3 loading. The BET surface area for pure silica support was 606 m2 g−1 and the pore size distribution in the range 40–80 A, showing the mesoporous nature of amorphous silica. The BET surface area decreased to 583 m2 g−1 with incorporation of 1% MoO3 and further decreased to 180 m2 g−1 with increasing MoO3 loading up to 20%. Above 10% MoO3 loading, formation of crystalline MoO3 clusters on amorphous silica was observed. Ammonia-TPD showed a drastic increase in acid strength after addition of 1% MoO3 compared to pure silica support and the acid strength increased with increasing MoO3 content. Among the series of catalysts prepared, MoO3/SiO2 containing 20 mol% MoO3 was found to be the most active catalyst for benzene nitration, without showing any deactivation after more than 1000 h, showing a very high potential for commercialization. |
| Databáze: | OpenAIRE |
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