Samarium-exchanged Heteropoly Tungstate: An Efficient Solid Acid Catalyst for the Synthesis of Glycerol Carbonate from Glycerol and Benzylation of Anisole

Samarium‐exchanged heteropoly tungstate (SmxTPA) is an efficient catalyst for the synthesis of glycerol carbonate from glycerol and urea. The catalysts with varying Sm content were prepared and characterized by FT‐IR spectroscopy, XRD, laser Raman spectroscopy, temperature‐programmed desorption of a...

Full description

Saved in:
Bibliographic Details
Published inChemCatChem Vol. 4; no. 9; pp. 1360 - 1367
Main Authors Kumar, Ch. Ramesh, Jagadeeswaraiah, K., Prasad, P. S. Sai, Lingaiah, N.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.09.2012
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Samarium‐exchanged heteropoly tungstate (SmxTPA) is an efficient catalyst for the synthesis of glycerol carbonate from glycerol and urea. The catalysts with varying Sm content were prepared and characterized by FT‐IR spectroscopy, XRD, laser Raman spectroscopy, temperature‐programmed desorption of ammonia, and X‐ray photo electron spectroscopy. The activity of the catalysts is related to the Lewis and Brønsted acidity, which depends on the Sm content in the catalysts. Partially exchanged SmxTPA catalyst showed high activity, owing to a higher number of Lewis acidic sites. The catalyst exhibited consistent activity and selectivity during recycling. A plausible reaction mechanism is presented. The catalyst also exhibited high activity in the acid‐catalyzed benzylation of anisole. It′s all about the exchange: Smexchanged heteropoly tungstate catalyzes the synthesis of glycerol carbonate from glycerol and urea. The catalyst activity is related to the Lewis and Brønsted acidity, which depends on the Sm content in the catalysts. Partially exchanged SmxTPA catalyst showed high activity, owing to a higher number of Lewis acidic sites. The catalyst also exhibited high activity in the acidcatalyzed benzylation of anisole.
Bibliography:ArticleID:CCTC201200110
Council of Scientific and Industrial Research (CSIR)
ark:/67375/WNG-LVG9SK74-9
istex:7B9C9E1000DE6F94735240FEAE59954C5E75ACF2
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.201200110