Selective alkylation of aniline to N-methyl aniline using chromium manganese ferrospinels
Data(s) |
01/09/2011
01/09/2011
2004
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Resumo |
Various compositions of chromium manganese ferrospinels were tested as catalysts for the vapour phase alkylation of aniline with methanol. The samples were prepared by room temperature co-precipitation technique and characterized by various physico-chemical methods. The acidity–basicity determination revealed that the samples possess greater amount of basic sites than acidic sites. All the ferrite samples proved to be selective and active for N-monoalkylation of aniline leading to N-methyl aniline; Cr0.6Mn0.4Fe2O4, Cr0.8Mn0.2Fe2O4 and CrFe2O4 exhibited cent percent selectivity for N-methyl aniline. Neither C-alkylated products nor any other side products were detected for all catalyst samples. The catalytic activity of the samples studied in this reaction is related to their acid–base properties and also on the cation distribution. Under the optimized reaction conditions all the systems showed constant activity for a long duration. |
Identificador |
1381-1169 http://dyuthi.cusat.ac.in/purl/2252 http://www.sciencedirect.com/science/article/pii/S1381116903005880 |
Idioma(s) |
en |
Publicador |
Elsevier |
Palavras-Chave | #Ferrospinels #Lewis acidity #Spinel ferrites #Aniline alkylation #N-Monoalkylation |
Tipo |
Working Paper |