Issue 16, 2017

One-pot integrated processing of biopolymers to furfurals in molten salt hydrate: understanding synergy in acidity

Abstract

The manufacture of furfural and 5-hydroxymethylfurfural (HMF), promising renewable platforms for bio-products, with high carbon efficiency is a challenge because of their undesired polymerization to humins. Here, we present an integrated process in inorganic salt solution to overcome this challenge. First, sugar biopolymers yield high monosaccharides (>90%) via efficient saccharification at low temperature. Second, monosaccharides in hydrolysates undergo efficient dehydration in biphasic solvents, assisted by the Brønsted acidity of the salt solution and the added inorganic Lewis acid. The salt solution exhibits high carbon efficiency in furfural and 5-hydroxymethylfurfural (HMF) products (>80 mol%) when compared with the analogous non-salt systems due to the cooperativity of the dual acidity and the higher viscosity of the salt solution than water and the concurrent reactive extraction of products. The process integration makes the separation of the aqueous phase easy, demonstrating nearly comparative activity upon recycling. Intact lignocellulose also achieves high yields of the dehydration products via one-pot depolymerization and saccharification, followed by dehydration. In addition, we elucidate the reasons for the high saccharification efficiency of the salt solution by correlating the effective acidity from the electrode potential and Hammett acidity measurements.

Graphical abstract: One-pot integrated processing of biopolymers to furfurals in molten salt hydrate: understanding synergy in acidity

Supplementary files

Article information

Article type
Paper
Submitted
12 Jun 2017
Accepted
19 Jul 2017
First published
19 Jul 2017

Green Chem., 2017,19, 3888-3898

One-pot integrated processing of biopolymers to furfurals in molten salt hydrate: understanding synergy in acidity

S. Sadula, O. Oesterling, A. Nardone, B. Dinkelacker and B. Saha, Green Chem., 2017, 19, 3888 DOI: 10.1039/C7GC01709J

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