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Selective Electrogenerative Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Furandialdehyde

ChemSusChem, 2017
Abstract2,5‐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
openaire   +2 more sources

Effect of MnO2 Crystal Structure on Aerobic Oxidation of 5-Hydroxymethylfurfural to 2,5-Furandicarboxylic Acid.

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

Platinum Catalyzed Oxidation of 5-Hydroxymethylfurfural

1990
The 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.
openaire   +1 more source

Electrocatalytic Refinery of Biomass-Based 5-Hydroxymethylfurfural to Fine Chemicals

ACS Catalysis, 2023
Yingjie Gao   +5 more
semanticscholar   +1 more source

Acrylamid und 5‐Hydroxymethylfurfural in Trockenfrüchten

Lebensmittelchemie, 2023
I. Richter   +4 more
openaire   +1 more source

Rationally designed Au-ZrOx interaction for boosting 5-hydroxymethylfurfural oxidation

Chemical Engineering Journal, 2023
Yunlei Zhang   +8 more
semanticscholar   +1 more source

Anionic defects engineering of NiCo2O4 for 5-hydroxymethylfurfural electrooxidation

Chemical Engineering Journal, 2023
Sixian Yang   +8 more
semanticscholar   +1 more source

The formation of 5-hydroxymethylfurfural from hexoses

Australian Journal of Chemistry, 1966
In 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
openaire   +1 more source

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