Results 241 to 250 of about 12,466,864 (267)
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Selective Electrogenerative Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Furandialdehyde
ChemSusChem, 2017Abstract2,5‐furandialdehyde (DFF) was synthesized by electrogenerative oxidation of 5‐hydroxymethylfurfural (HMF) over a PtRu catalyst with 89 % selectivity at 50 °C after 17 h. This approach opens an avenue for a selective, energy‐efficient and green oxidation of biomass‐derived platform alcohols to added‐value chemicals.
Tao Cao +6 more
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Journal of the American Chemical Society, 2019
Aerobic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) as a bioplastics monomer is efficiently promoted by a simple system based on a nonprecious-metal catalyst of MnO2 and NaHCO3.
E. Hayashi +6 more
semanticscholar +1 more source
Aerobic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) as a bioplastics monomer is efficiently promoted by a simple system based on a nonprecious-metal catalyst of MnO2 and NaHCO3.
E. Hayashi +6 more
semanticscholar +1 more source
Platinum Catalyzed Oxidation of 5-Hydroxymethylfurfural
1990The liquid phase oxidation of 5-hydroxymethylfurfural (HMF) over platinum on alumina catalysts is described. The main intermediate is 5-formyl-2-furan-carboxylic acid (FFCA), indicating that the hydroxymethyl group of HMF is oxidized first in the presence of the aldehyde group.
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Electrocatalytic Refinery of Biomass-Based 5-Hydroxymethylfurfural to Fine Chemicals
ACS Catalysis, 2023Yingjie Gao +5 more
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Acrylamid und 5‐Hydroxymethylfurfural in Trockenfrüchten
Lebensmittelchemie, 2023I. Richter +4 more
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Rationally designed Au-ZrOx interaction for boosting 5-hydroxymethylfurfural oxidation
Chemical Engineering Journal, 2023Yunlei Zhang +8 more
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Anionic defects engineering of NiCo2O4 for 5-hydroxymethylfurfural electrooxidation
Chemical Engineering Journal, 2023Sixian Yang +8 more
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The formation of 5-hydroxymethylfurfural from hexoses
Australian Journal of Chemistry, 1966In the acid catalysed conversion of hexoses to furans, the yield of 2- furyl hydroxymethyl ketone (FHK) relative to that of 5- hydroxymethylfurfural (HMF) is the same when either glucose or fructose is used as the starting material. The significance of this result is discussed in relation to the various reaction mechanisms proposed for the formation of
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