Selective alkylation of aniline to N-methyl aniline using chromium manganese ferrospinels

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Selective alkylation of aniline to N-methyl aniline using chromium manganese ferrospinels

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dc.contributor.author Nishamol, K
dc.contributor.author Rahna, K S
dc.contributor.author Sugunan, S
dc.date.accessioned 2011-09-01T08:41:25Z
dc.date.available 2011-09-01T08:41:25Z
dc.date.issued 2004
dc.identifier.issn 1381-1169
dc.identifier.uri http://dyuthi.cusat.ac.in/purl/2252
dc.description.abstract 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. en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.subject Ferrospinels en_US
dc.subject Lewis acidity en_US
dc.subject Spinel ferrites en_US
dc.subject Aniline alkylation en_US
dc.subject N-Monoalkylation en_US
dc.title Selective alkylation of aniline to N-methyl aniline using chromium manganese ferrospinels en_US
dc.type Working Paper en_US
dc.contributor.faculty Science en_US
dc.identifier.url http://www.sciencedirect.com/science/article/pii/S1381116903005880 en_US


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