Abstract
Using cellulosic biomass to synthesize bulk quantities of high-value chemicals is of great interest for developing a sustainable biobased society. Especially, direct catalytic conversion of cellulose to glycols, important building blocks for polymers, remains a grand challenge. Herein, we report the development of a versatile binary nickel-lanthanum(III) catalyst for the conversion of cellulose to both ethylene glycol (EG) and propylene glycol (1,2-PG) in a yield of 63.7%, which is one of the best performances reported for this catalytic reaction. Especially, lanthanum(III) exhibited a high level of activity toward the degradation of cellulose (TON = 339) at a very low concentration (0.2 mmol/L). On the basis of density functional theory calculations and experimental analyses, we addressed a dual route for this catalytic mechanism: a major route involving the selective cracking of sugars into C2 molecules and a minor route involving the hydrogenolysis of sugar alcohols. Lanthanum(III) catalyzes the cleavage of the C2-C3 bond in glucose via sequential epimerization and 2,3-hydride shift reactions to form glycolaldehyde, the precursor of EG.
Original language | English |
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Pages (from-to) | 874-883 |
Number of pages | 10 |
Journal | ACS Catalysis |
Volume | 5 |
Issue number | 2 |
DOIs | |
State | Published - 6 Feb 2015 |
Externally published | Yes |
Keywords
- cellulose
- dual route
- ethylene glycol
- nickel-lanthanum catalyst
- propylene glycol
- theoretical calculation