Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/7097
Full metadata record
DC FieldValueLanguage
dc.contributor.authorD’Souza, Joyce-
dc.contributor.authorNagaraju, N-
dc.date.accessioned2010-01-07T06:43:25Z-
dc.date.available2010-01-07T06:43:25Z-
dc.date.issued2006-11-
dc.identifier.issn0975-0991 (Online); 0971-457X (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/7097-
dc.description605-613en_US
dc.description.abstractThe catalytic activity of zirconia, alumina and silica and their sulphate, phosphate and borate modified forms has been studied in the liquid phase esterification of benzyl alcohol with acetic acid for the synthesis of benzyl acetate. All these catalysts have been found to be active for the formation of benzyl acetate with 100% selectivity. A small amount of dibenzyl ether was formed only in the case of sulphated zirconia when refluxed for more than 12 h. The active sites with ‘weak to intermediate’ acid strengths may be responsible for the catalytic activity towards the esterification. Sulphated zirconia is the most suitable catalyst providing 53 to 90% yield of benzyl acetate when refluxed for 30 min to 24 h with 0.1 to 3 g of the catalyst. This catalyst has been found to be effective in catalyzing the esterification of n-propanol, iso-propanol, n-butanol and iso-butanol with acetic acid to form the respective esters in good yields.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesC07C27/22, C07C27/00en_US
dc.sourceIJCT Vol.13(6) [November 2006]en_US
dc.subjectEsterificationen_US
dc.subjectBenzyl acetateen_US
dc.subjectSolid acidsen_US
dc.subjectSulphateen_US
dc.subjectBorateen_US
dc.subjectPhosphate-modified zirconiaen_US
dc.subjectAlumina and silicaen_US
dc.titleCatalytic activity of anion-modified zirconia, alumina and silica in the esterification of benzyl alcohol with acetic aciden_US
dc.typeArticleen_US
Appears in Collections:IJCT Vol.13(6) [November 2006]

Files in This Item:
File Description SizeFormat 
IJCT 13(6) 605-613.pdf658.13 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.