The development of greener extraction systems is essential to improving the sustainability of biomass valorization processes. Here we report that 5-hydroxymethylfurfural (HMF) and levulinic acid (LEV)─two bioderived platform molecules often coproduced in biomass processing─spontaneously form a stable liquid phase over a broad compositional range. Differential scanning calorimetry (DSC) and thermodynamic modeling reveal a eutectic composition near xHMF = 0.39 with a melting temperature of 258 K and significant negative deviation from ideal behavior. The mixture remains liquid across a wide compositional range even in the presence of low water content (0.3–1.0 wt %), exhibiting deep eutectic solvent (DES)-like behavior. Structural and dynamic analyses using DSC, NMR spectroscopy, molecular dynamics (MD) and density functional theory (DFT) calculations uncover a nonideal mixing regime driven by the network of HMF-LEV hydrogen bonding. Notably, water does not disrupt the HMF-LEV network but enhances its structuration at the eutectic composition by moderating LEV-LEV interactions and enabling more favorable HMF-LEV hydrogen bonding. This work shows that the liquid HMF-LEV phase can be generated in situ within a heterogeneous biomass surrogate, enabling substantially higher HMF extraction efficiencies than conventional solvents and eliminating the need for additional organic extractants. This provides a proof of concept for a solvent-minimized route to HMF recovery, indicating the HMF-LEV system as a promising, bioderived liquid platform with potential for integration into future resource-efficient biorefinery schemes.

Stable and Water-Tolerant Deep Eutectic Solvent from Biomass-Derived 5-Hydroxymethylfurfural (HMF) and Levulinic Acid

Righetti, Grazia Isa C.;Di Pietro, Maria Enrica;Vangosa, Francesco Briatico;Mele, Andrea
2026-01-01

Abstract

The development of greener extraction systems is essential to improving the sustainability of biomass valorization processes. Here we report that 5-hydroxymethylfurfural (HMF) and levulinic acid (LEV)─two bioderived platform molecules often coproduced in biomass processing─spontaneously form a stable liquid phase over a broad compositional range. Differential scanning calorimetry (DSC) and thermodynamic modeling reveal a eutectic composition near xHMF = 0.39 with a melting temperature of 258 K and significant negative deviation from ideal behavior. The mixture remains liquid across a wide compositional range even in the presence of low water content (0.3–1.0 wt %), exhibiting deep eutectic solvent (DES)-like behavior. Structural and dynamic analyses using DSC, NMR spectroscopy, molecular dynamics (MD) and density functional theory (DFT) calculations uncover a nonideal mixing regime driven by the network of HMF-LEV hydrogen bonding. Notably, water does not disrupt the HMF-LEV network but enhances its structuration at the eutectic composition by moderating LEV-LEV interactions and enabling more favorable HMF-LEV hydrogen bonding. This work shows that the liquid HMF-LEV phase can be generated in situ within a heterogeneous biomass surrogate, enabling substantially higher HMF extraction efficiencies than conventional solvents and eliminating the need for additional organic extractants. This provides a proof of concept for a solvent-minimized route to HMF recovery, indicating the HMF-LEV system as a promising, bioderived liquid platform with potential for integration into future resource-efficient biorefinery schemes.
2026
DES
HMF
Hydroxymethylfurfural
levulinic acid
molecular dynamics
NMR spectroscopy
phase-diagram
solid−liquid equilibrium
sustainable chemistry
File in questo prodotto:
File Dimensione Formato  
stable-and-water-tolerant-deep-eutectic-solvent-from-biomass-derived-5-hydroxymethylfurfur.pdf

accesso aperto

: Publisher’s version
Dimensione 4.53 MB
Formato Adobe PDF
4.53 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/1313046
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 1
  • ???jsp.display-item.citation.isi??? 1
social impact