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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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