Conversion of Sugars to Lactic Acid Derivatives Using Heterogeneous Zeotype Catalysts
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- 30 April 2010
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 328 (5978), 602-605
- https://doi.org/10.1126/science.1183990
Abstract
Presently, very few compounds of commercial interest are directly accessible from carbohydrates by using nonfermentive approaches. We describe here a catalytic process for the direct formation of methyl lactate from common sugars. Lewis acidic zeotypes, such as Sn-Beta, catalyze the conversion of mono- and disaccharides that are dissolved in methanol to methyl lactate at 160°C. With sucrose as the substrate, methyl lactate yield reaches 68%, and the heterogeneous catalyst can be easily recovered by filtration and reused multiple times after calcination without any substantial change in the product selectivity.Keywords
This publication has 29 references indexed in Scilit:
- Zeolite‐Catalyzed Isomerization of Triose SugarsChemSusChem, 2009
- Catalytic Processing of Lactic Acid over Pt/Nb2O5ChemSusChem, 2009
- The Renewable Chemicals IndustryChemSusChem, 2008
- Metal Chlorides in Ionic Liquid Solvents Convert Sugars to 5-HydroxymethylfurfuralScience, 2007
- Chemical Routes for the Transformation of Biomass into ChemicalsChemical Reviews, 2007
- Biomass Recalcitrance: Engineering Plants and Enzymes for Biofuels ProductionScience, 2007
- Predicting the Activity of Single Isolated Lewis Acid Sites in Solid CatalystsChemistry – A European Journal, 2006
- Phase Modifiers Promote Efficient Production of Hydroxymethylfurfural from FructoseScience, 2006
- Synthesis of Transportation Fuels from Biomass: Chemistry, Catalysts, and EngineeringChemical Reviews, 2006
- Single‐Site Heterogeneous CatalystsAngewandte Chemie International Edition, 2005