Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/39996
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dc.contributor.authorChandrakala, M-
dc.contributor.authorRao, R Ramachandra-
dc.contributor.authorKulkarni, S J-
dc.contributor.authorSubrahmanyam, M-
dc.contributor.authorRaghavan, K V-
dc.date.accessioned2017-02-01T09:48:40Z-
dc.date.available2017-02-01T09:48:40Z-
dc.date.issued1998-04-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/39996-
dc.description323-327en_US
dc.description.abstractThe reaction of n-butanol, formaldehyde and ammonia has been carried out over modified ZSM-S catalysts, to get 3,S diethylpyridine selectively. Among all the catalysts ZrZSM-5 has shown high activity with 73.4 wt% of 3,5-diethylpyridine at 97.0 wt% conversion of n- butanol. The effects of temperature, WHSV and molar ratio have been studied in the synthesis of 3,S-diethylpyridine over ZrZSM-S. The other major products are lutidines and collidines. Our studies have shown that modified ZSM-S catalysts can be used for the synthesis of pyridine and substituted pyridines from various alcohols or aldehydes via dehydrocyclization and dehydrogenation.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.37A(04) [April 1998]en_US
dc.titleSelective preparation of 3,5-diethylpyridine from n-butanol, formaldehyde and ammonia over modified ZSM-5 catalystsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.37A(04) [April 1998]

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