Levoglucosenone
From Wikipedia, the free encyclopedia
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| Names | |
|---|---|
| Preferred IUPAC name
(1S,5R)-6,8-Dioxabicyclo[3.2.1]oct-2-en-4-one[1] | |
| Systematic IUPAC name
1,6-Anhydro-3,4-dideoxy-β-d-glycero-hex-3-enoyranos-2-ulose[2] | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChemSpider | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C6H6O3 | |
| Molar mass | 126.111 g·mol−1 |
| Appearance | yellow liquid |
| Density | 1.304 g/cm3 (20 °C) [3] |
| Boiling point | 231 °C; 448 °F; 504 K[3] |
| Vapor pressure | 6.2 Pa (25 °C) [3] |
Refractive index (nD) |
1.5065 (20 °C)[3] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Levoglucosenone is an organic compound with the formula [OCH2(CH)4CO2]. A pale yellow liquid, it is an unsaturated bicyclic ketone-diether formed from levoglucosan by loss of two molecules of water. As a product of the acid-catalysed pyrolysis of cellulose, D-glucose, and levoglucosan, this liquid hydrocarbon is of interest as a biofuel and biofeedstock.[4]
The compound was first identified in 1970 as a product of the thermal decomposition of cellulose.[5]
The primary way of obtaining levoglucosenone is via pyrolysis of carbohydrates, particularly cellulose. Levoglucosenone can be derived from biomass or from other cellulosic materials including domestic/commercial waste paper. The availability of multiple sources is a key advantage when compared to other platform chemicals which are solely derived from biomass.
The title compound is produced when cellulose is heated above 170 °C with sulfuric acid with various additives.[4] Alongside levoglucosenone as a major product, 2-furfuraldehyde is sometimes formed in 5-10%. The bio-oil can be vacuum distilled, resulting in purified levoglucosenone.[6] The use of polar, aprotic solvents such as THF, γ-valerolactone and sulfolane has been found to improve pyrolytic yields, as the solvents cause swelling of the cellulose and inhibit repolymerisation back to levoglucosan. These solvents also promote catalytic dehydration of levoglucosan to levoglucosenone.[7]
Microwave irradiation of microcrystalline cellulose can also be used to produce levoglucosenone.[8]
Cellulose-containing waste from biorefineries can also be converted into 6-8% LGO under microwave irradiation in addition to the usual decomposition products such as hydroxymethylfurfural HMF, formic acid, formaldehyde, CO2 and water.[9]