Conversion of highly concentrated fructose into 5-hydroxymethylfurfural by acid–base bifunctional HPA nanocatalysts induced by choline chloride

Abstract

A series of acid–base bifunctional heteropolyacids (HPAs) (C6H15O2N2)3−xHxPW12O40 (abbreviated as Ly3−xHxPW) have been designed using different ratios of HPAs with amino acid lysine in order to control their acid–base properties. The amino acid group facilitated the HPAs forming micellar assemblies in choline chloride–fructose deep eutectic solvents. In the dehydration of fructose to 5-hydroxymethylfurfural (HMF), Ly3−xHxPW exhibited different catalytic activities because of their different acid–base properties. Among all the HPA catalysts, Ly2HPW gave the best results with 93.3% conversion and 92.3% HMF yield within a very short time, i.e. 1 min under the conventional temperature of 110 °C using choline chloride (ChCl) as solvent, and this was almost the best result by far. The highest activity and selectivity of Ly2HPW came from the synergistic effect between certain acidic and basic capacities, which provides ready accessibility to the nucleophilic (–NH2) and electrophilic (H) sites. Moreover, this catalyst was tolerant to highly concentrated feedstock (∼66.7 wt%) with the additive ChCl. Ly2HPW performed as a heterogeneous catalyst in the ChCl system and could be recycled by simple washing treatment.