Biofuels From Lignocellulosic Biomass 2016
DOI: 10.1002/9783527685318.ch7
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Cited by 8 publications
(17 citation statements)
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“…Indeed, these systems possess physicochemical properties (i.e., high octane number, high boiling point, poor miscibility with water) close to those of conventional fuels, which makes them promising biofuel candidates. [114] 3 ). [114] Furthermore, the low market price of furfural makes the hydrogenation-hydrogenolysis of FU an attractive route to obtain 2-MF (Scheme 4).…”
Section: Lohcs In Furan-based Fuels and Additives Productionmentioning
confidence: 99%
See 1 more Smart Citation
“…Indeed, these systems possess physicochemical properties (i.e., high octane number, high boiling point, poor miscibility with water) close to those of conventional fuels, which makes them promising biofuel candidates. [114] 3 ). [114] Furthermore, the low market price of furfural makes the hydrogenation-hydrogenolysis of FU an attractive route to obtain 2-MF (Scheme 4).…”
Section: Lohcs In Furan-based Fuels and Additives Productionmentioning
confidence: 99%
“…[114] 3 ). [114] Furthermore, the low market price of furfural makes the hydrogenation-hydrogenolysis of FU an attractive route to obtain 2-MF (Scheme 4).…”
Section: Lohcs In Furan-based Fuels and Additives Productionmentioning
confidence: 99%
“…2,5-Dimethylfuran (2,5-DMF) (Chart 1) has become attractive as a biofuel candidate because of its physicochemical properties which are very close to that of conventional fuels. 107 For example, it shows an octane number (119) higher than those of gasoline and ethanol, low water solubility (0.26%), and high boiling point (92−94 °C). The preferred pathway for the synthesis of 2,5-DMF starts at 5hydroxymethylfurfural (5-HMF), which, analogously to LA, is identified as a biomass-based platform molecule.…”
Section: ■ Introductionmentioning
confidence: 99%
“…45 5-HMF can be synthesized from fructose, glucose, or polysaccharides through dehydration; the conversion of HMF to DMF proceeds through hydrogenation followed by the hydrogenolysis of the hydroxyl groups of the 2,5-hydroxymethyl furan intermediate. 107 Saha et al 108 explored the formation of 2,5-dimethylfuran (DMF) from different sources, i.e., fructose, α-cellulose, sugar cane bagasse, and agar, using FA as the hydrogen source. More specifically, the reaction involved two steps: (i) the formation of Two significant examples demonstrating the efficiency of a Pd/C catalyst have been reported by Rauchfuss and coworkers 109,110 When using 5 mol % Pd/C, 109 an excess of FA (10 equiv), and dioxane as solvent, an HMF conversion value of 95% was achieved (120 °C).…”
Section: ■ Introductionmentioning
confidence: 99%
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