Results 131 to 140 of about 12,466,864 (267)

5-Hydroxymethylfurfural Oxidation over Supported Metal Catalysts

, 2016
One molecule often cited as a key building block chemical in the development of a biorenewables-based chemicals industry is 5-hydroxymethylfurfural (HMF). Derived from fructose and glucose, HMF can be oxidized to 2,5-furandicarboxylic acid (FDCA), a potential replacement for the non-renewable polyethylene terephthalate monomer comprising PET plastics ...
openaire   +2 more sources

Reactor engineering for the enzymatic synthesis of 5-hydroxymethylfurfural stearate in a batch bioreactor and a packed bed flow bioreactor. [PDF]

Bioresour Bioprocess
Guajardo N, Gajardo-Parra N, Cea-Klapp E, Canales R, Lienqueo ME, Sandoval G.   +5 more
europepmc   +1 more source

Stable and Water-Tolerant Deep Eutectic Solvent from Biomass-Derived 5‑Hydroxymethylfurfural (HMF) and Levulinic Acid. [PDF]

ACS Sustain Chem Eng
Righetti GIC, Rozas S, Di Pietro ME, Santamaría S, Nasrallah S, Minceva M, Vangosa FB, Aparicio S, Mele A.   +8 more
europepmc   +1 more source

Ligand-Wise Stripping Dictates Metal Ensemble Catalysts for Selective Oxidation of Biomass-Derived 5-Hydroxymethylfurfural. [PDF]

Nanomicro Lett
Li J, Wang G, Wu Y, Song C, Pang T, Zhuang Z, Yang J, Sui W, Lin L, Wang D, Wang L, Si C.   +11 more
europepmc   +1 more source

Advance biocatalyst for the green conversion of 5-hydroxymethylfurfural to a biopolymer precursor 2,5-furandicarboxylic acid. [PDF]

Biotechnol Biofuels Bioprod
Pawar L, Kumar P, Dhiman R, Mittal D, Kumar A, Purohit R, Yadav SK.   +6 more
europepmc   +1 more source

Herstellung von 5‐Hydroxymethylfurfural aus D‐Fructose [PDF]

Chemie Ingenieur Technik, 2006
J. Lifka, B. Ondruschka, A. Stark
openaire   +1 more source

Natural-based catalysts for 5-hydroxymethylfurfural production from cane syrup for pharmaceutical applications. [PDF]

RSC Adv
Akkarawatkhoosith N, Suknasaeng R, Chaiyasit Y, Jaree A, Tongtummachat T.   +4 more
europepmc   +1 more source

5-Hydroxymethylfurfural: A Particularly Harmful Molecule Inducing Toxic Lipids and Proteins? [PDF]

Molecules
Greilberger J, Feigl G, Greilberger M, Bystrianska S, Greilberger M.   +4 more
europepmc   +1 more source

EFSA ; Scientific Opinion on Flavouring Group Evaluation 66, Revision 1 (FGE.66Rev1): Consideration of Furfuryl Alcohol and Related Flavouring Substances Evaluated by JECFA (55th meeting) [PDF]

, 2011

core   +1 more source

Co-sputtered CuNi heteroatomic electrocatalyst for enhanced 5-hydroxymethylfurfural selective electrochemical conversion. [PDF]

Sci Rep
Dikshit M, Muchharla B, Rivera LV, Kumar K, Sanwaria S, Sadasivuni KK, Karoui A, Kumar S, Adedeji A, Kumar B.   +9 more
europepmc   +1 more source