5-hydroxymethylfurfural
(5-HMF) is a promising high value-added
platform chemical, which can be produced from glucose, fructose, or
lignocellulosic biomass via catalysis technology. However, the effective
separation of 5-HMF from aqueous solution and actual biomass hydrolysate
is still challenging because 5-HMF can be further rehydrated into
levulinic acid (LA) and formic acid (FA) under acidic conditions.
Herein, the adsorption behavior of glucose and 5-HMF and its follow-up
products (LA and FA) from aqueous solutions onto polymeric adsorbents
modified with various functional groups (XAD-4, XAD7HP, and XAD761
resins) was systematically investigated. The results showed that XAD761
resin exhibited the highest adsorption selectivity (α5‑HMF/glucose = 42.42 ± 5.84, α5‑HMF/FA = 18.41 ±
0.50, and α5‑HMF/LA = 3.01 ± 0.10) and
capacity for 5-HMF (106 mg g–1 wet resin). The adsorption
equilibrium was better fitted by the Freundlich isotherm model at
the studied range of 5-HMF concentrations. The thermodynamic study
and activation energy also revealed that the adsorption process of
XAD761 resin for 5-HMF was spontaneous, exothermic, and physical.
The kinetic regression results revealed that the kinetic data of 5-HMF
was accurately followed by the pseudo-second-order kinetic model.
In conclusion, the present study revealed that the potential of phenol
formaldehyde resin with hydroxyl groups could be used as an adsorbent
for aldehyde organic compounds.