Oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) was carried out over Ru/Al2O3 using O2 aqueous alkaline solutions in a trickle-bed reactor. HMF was completely converted at 140 °C, 30 bar O2, resulting in 98% FDCA selectivity (pH 11, GHSV = 900 h–1, WHSV = 1 h–1). At 140 °C, FDCA was the main product under all conditions. Alkali (nature and concentration) played a significant role in oxidation or degradation of HMF. The selectivity to oxidized compounds was favored using Na2CO3 by accelerating oxidation steps, principally to the aldehyde group maintaining an appropriate pH for the reaction. The estimated kinetic parameters obtained were statistically significant, suggesting an accurate representation of the sy...
Selective catalytic oxidation of carbohydrate-derived 5-hydroxymethylfurfural, furfuryl alcohol, and...
Oxidation of 5-hydroxymethylfurfural (HMF) using air or pure oxygen was performed in polytetrafluoro...
Selective oxidation of furfural to furoic acid was performed with pure oxygen in aqueous phase under...
The catalytic activity of a simple Au/AlO catalytic system prepared by the direct anionic exchange (...
An effective and selective method for the oxidation of 5-hydroxymethylfurfural (HMF) by using hydrog...
2,5-Furandicarboxylic (FDCA) is a potential substitute for petroleum-derived terephthalic acid, and ...
The reaction mechanism of 5-hydroxymethylfurfural (HMF) oxidation in neutral aqueous solution with O...
Funding Information: Financial support from the Natural Science Foundation of China under Contracts ...
An acetal protection strategy for (5-hydroxymethyl)furfural (HMF) was used to obtain 2,5-diformyfura...
5-Hydroxymethylfurfural (HMF) is an important biomass-based platform chemical, and its selective aer...
The selective oxidation of 5-hydroxymethyl-2-furaldehyde (HMF) to furan-2,5-dicarboxaldehyde (FDA) h...
The oxidation of 5-hydroxymethylfurfural (HMF), an important platform chemical from biomass feedstoc...
In this paper, 2,5-furandicarboxylic acid (FDCA) was efficiently prepared by the direct oxidation of...
Furanic di-carboxylate derivatives of 5-Hydroxymethylfurfural (HMF) are nowadays important in the po...
SSCI-VIDE+CDFA+NES:MBEInternational audiencePt catalysts prepared over different metallic oxide supp...
Selective catalytic oxidation of carbohydrate-derived 5-hydroxymethylfurfural, furfuryl alcohol, and...
Oxidation of 5-hydroxymethylfurfural (HMF) using air or pure oxygen was performed in polytetrafluoro...
Selective oxidation of furfural to furoic acid was performed with pure oxygen in aqueous phase under...
The catalytic activity of a simple Au/AlO catalytic system prepared by the direct anionic exchange (...
An effective and selective method for the oxidation of 5-hydroxymethylfurfural (HMF) by using hydrog...
2,5-Furandicarboxylic (FDCA) is a potential substitute for petroleum-derived terephthalic acid, and ...
The reaction mechanism of 5-hydroxymethylfurfural (HMF) oxidation in neutral aqueous solution with O...
Funding Information: Financial support from the Natural Science Foundation of China under Contracts ...
An acetal protection strategy for (5-hydroxymethyl)furfural (HMF) was used to obtain 2,5-diformyfura...
5-Hydroxymethylfurfural (HMF) is an important biomass-based platform chemical, and its selective aer...
The selective oxidation of 5-hydroxymethyl-2-furaldehyde (HMF) to furan-2,5-dicarboxaldehyde (FDA) h...
The oxidation of 5-hydroxymethylfurfural (HMF), an important platform chemical from biomass feedstoc...
In this paper, 2,5-furandicarboxylic acid (FDCA) was efficiently prepared by the direct oxidation of...
Furanic di-carboxylate derivatives of 5-Hydroxymethylfurfural (HMF) are nowadays important in the po...
SSCI-VIDE+CDFA+NES:MBEInternational audiencePt catalysts prepared over different metallic oxide supp...
Selective catalytic oxidation of carbohydrate-derived 5-hydroxymethylfurfural, furfuryl alcohol, and...
Oxidation of 5-hydroxymethylfurfural (HMF) using air or pure oxygen was performed in polytetrafluoro...
Selective oxidation of furfural to furoic acid was performed with pure oxygen in aqueous phase under...