Please use this identifier to cite or link to this item: https://doi.org/10.1002/cctc.201000300
Title: Effects of Acidity and Pore Size Constraints on Supported Niobium Oxide Catalysts for the Selective Formation of Glycerol Monolaurate
Authors: Radhakrishnan, R.
Wu, J.
Jaenicke, S. 
Chuah, G.K. 
Keywords: Acidity
Heterogeneous catalysis
Mesoporous materials
Sustainable chemistry
Issue Date: 11-Apr-2011
Citation: Radhakrishnan, R., Wu, J., Jaenicke, S., Chuah, G.K. (2011-04-11). Effects of Acidity and Pore Size Constraints on Supported Niobium Oxide Catalysts for the Selective Formation of Glycerol Monolaurate. ChemCatChem 3 (4) : 761-770. ScholarBank@NUS Repository. https://doi.org/10.1002/cctc.201000300
Abstract: Supported niobium oxide catalysts with 5-30wt.% Nb2O5 were prepared by grafting niobium ethoxide onto MCM-41 and hydrous zirconia. The supported samples contain Brønsted-acid sites, whereas bulk niobium oxide has predominantly Lewis-acid sites. In the esterification of glycerol with lauric acid, good activity and a high glycerol monolaurate selectivity was achieved when the active niobium oxide phase was coated within the pore channels of an MCM-41 support, which has a mean pore diameter of 2.2nm. Phosphated Nb2O5/MCM-41 showed an even higher activity without any penalty in selectivity, enabling monolaurate yields of 89-90%. Glycerol monolaurate is an important ingredient in the food, pharmaceutical, and cosmetic industries. A key feature of these pore confined catalysts is the sustained high selectivity to monolaurate even at high conversions. In contrast, niobium oxide supported on wide-pored hydrous zirconia showed lower selectivity. The catalysts are active in the solventless esterification of a number of alcohols and acids and can be easily recycled for subsequent batch reactions, making them attractive as green catalysts for sustainable processes. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Source Title: ChemCatChem
URI: http://scholarbank.nus.edu.sg/handle/10635/93661
ISSN: 18673880
DOI: 10.1002/cctc.201000300
Appears in Collections:Staff Publications

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