Conversion of furfuryl alcohol to ethyl levulinate using porous aluminosilicate acid catalysts

•Conversion of furfuryl alcohol into ethyl levulinate using aluminosilicate acid catalysts.•Identification of reaction products by GC×GC-ToFMS analyses.•Ether, acetal, ester by-products from the non-productive consumption of ethanol.•Comparative study of catalytic performances of aluminosilicates an...

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Bibliographic Details
Published in:Catalysis today Vol. 218-219; pp. 76 - 84
Main Authors: Neves, Patrícia, Lima, Sérgio, Pillinger, Martyn, Rocha, Sílvia M., Rocha, João, Valente, Anabela A.
Format: Journal Article
Language:English
Published: Elsevier B.V 01-12-2013
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Summary:•Conversion of furfuryl alcohol into ethyl levulinate using aluminosilicate acid catalysts.•Identification of reaction products by GC×GC-ToFMS analyses.•Ether, acetal, ester by-products from the non-productive consumption of ethanol.•Comparative study of catalytic performances of aluminosilicates and Amberlyst™-15. The following porous aluminosilicates were tested as acid catalysts in the reaction of furfuryl alcohol (FA) with ethanol, at 140°C: micro/mesoporous composite Beta/TUD-1 and the correspondent nanocrystalline (large pore) zeolite H-Beta; ITQ-2 and its zeolite counterpart (medium pore) H-MCM-22; mesoporous Al-TUD-1. The target product ethyl levulinate (EL) was formed with a yield up to 80%, at 24h reaction (100% FA conversion). Relationships between the catalytic results and the acid and texture properties of the catalysts were established. Comparative studies for the aluminosilicates and the well-known sulfonic acid resin Amberlyst™-15 were reported on the basis of EL yields, the undesirable formation of diethyl ether, and catalyst stability (regeneration and reuse). A study of the reaction products was carried out by comprehensive two-dimensional gas chromatography combined with time-of-flight mass spectrometry.
ISSN:0920-5861
1873-4308
DOI:10.1016/j.cattod.2013.04.035