April 5, 2024
Journal Article

Theoretical Insights on the Fragmentation of Cellulosic Oligomers to form Hydroxyacetone and Hydroxyacetaldehyde

Abstract

The presence of heavy unknown oligomeric sugar products in bio-oil is evidenced in experimental results reported in the literature. In this paper, we study the fragmentation reactions yielding acetol and glycolaldehyde from oligomeric sugars following previous work on dehydration reactions to propose structures of these oligomers. Acetol and glycolaldehyde are primary products of cellulose fast pyrolysis but the fragmentation reaction mechanism of these compounds from oligomers merits further study. The density functional theory (DFT) approach was employed to study this reaction. Results revealed that acetol and glycolaldehyde fragments are favorably removed from the non-reducing end based on their thermodynamic stabilities. Theoretical FTIR and NMR spectra were calculated to aid in understanding the structures of the oligomeric sugars. Also, the thermodynamics and physical properties of these compounds were estimated using the Group Contribution Method (GCM). These properties are essential in the design of processing technologies and the upgrading of products.

Published: April 5, 2024

Citation

Denson M.D., E. Terrell, P. Kostetskyy, L.J. Broadbelt, M.V. Olarte, and M. Garcia-Perez. 2023. Theoretical Insights on the Fragmentation of Cellulosic Oligomers to form Hydroxyacetone and Hydroxyacetaldehyde. Energy and Fuels 37, no. 18:13997–14005. PNNL-SA-181688. doi:10.1021/acs.energyfuels.3c01924