Room temperature synthesis of diphenylmethane over novel mesoporous Lewis acid catalysts
β Scribed by M. Selvaraj; T.G. Lee
- Book ID
- 104056909
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 260 KB
- Volume
- 243
- Category
- Article
- ISSN
- 1381-1169
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β¦ Synopsis
Highly selective synthesis of diphenylmethane (DPM) was carried out by Friedal-Crafts benzylation of benzene using benzyl chloride (BC) as alkylating agent in the presence of a flow of nitrogen under liquid phase reaction conditions over novel mesoporous SO 4 2-/Al-MCM-41 catalysts with different Si/Al ratios. For these reactions, the influences of various reaction parameters, such as different catalysts, reaction temperature, time, mmol ratios of reactants and recyclability are discussed. With increasing the Si/Al ratios of SO 4 2-/Al-MCM-41 catalysts from 21 to 83, the conversion of BC and selectivity of DPM decreased because the number of Lewis acid sites in SO 4 2-/Al-MCM-41 catalysts are found to decrease almost linearly with increasing ratios of Si/Al. Further the catalytic results were compared with those obtained by using 0.8N sulfuric acid, different Si/Al ratios of Al-MCM-41, HY, Hβ€, HM and H-ZSM-5 zeolites. From the comparison of the results, SO 4 2-/Al-MCM-41( 21) is found to be a highly active and recyclable heterogeneous catalyst for the highly selective synthesis of DPM. Thus, the selectivity of DPM in SO 4
2-/Al-MCM-41( 21) is higher than that in other SO 4
π SIMILAR VOLUMES
Aminocyclization reaction of 4-methyl acetophenone (4-MAP) with formaldehyde and ammonia was contacted under vapor phase reaction conditions over novel mesoporous Zn-Al-MCM-41 catalysts with different Si/(Zn + Al) ratios for highly selective synthesis of 2,6-BP (2,6-bis(4-methylphenyl)pyridine). For