Production of renewable p-xylene from 2,5-dimethylfuran via Diels-Alder cycloaddition and dehydrative aromatization reactions over silica-alumina aerogel catalysts

Authors
Wijaya, Yanuar PhilipSuh, Dong JinJae, Jungho
Issue Date
2015-10-05
Publisher
ELSEVIER SCIENCE BV
Citation
CATALYSIS COMMUNICATIONS, v.70, pp.12 - 16
Abstract
We report the selective conversion of biomass-derived 2,5-dimethylfuran (DMF) to p-xylene (similar to 70% selectivity) through Diels-Alder cycloaddition and subsequent dehydration with silica-alumina aerogel (SAA) catalysts. The high activity of SAA can be attributed to its high surface area, large mesoporous volume, and high acid site concentrations. The conversion of DMF and the yield of p-xylene were strongly dependent on the silica alumina ratio of SAA. A higher aluminum content in SAA led to a progressive increase in the concentration of Bronsted acid sites and a corresponding increase in the p-xylene production rate. The effect of solvent on the production of p-xylene was examined, and it was found that the p-xylene production rate increases significantly in polar aprotic solvents (i.e. 1,4-dioxane). (C) 2015 Elsevier B.V. All rights reserved.
Keywords
TEREPHTHALIC ACID; BIOMASS; CONVERSION; ETHYLENE; AROMATICS; FUELS; TEREPHTHALIC ACID; BIOMASS; CONVERSION; ETHYLENE; AROMATICS; FUELS; Cycloaddition; Diels-Alder; 2,5-Dimethylfuran; p-Xylene; Silica-alumina aerogels (SAA)
ISSN
1566-7367
URI
https://pubs.kist.re.kr/handle/201004/124901
DOI
10.1016/j.catcom.2015.07.008
Appears in Collections:
KIST Article > 2015
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