Issue 3, 2018

Universal kinetic solvent effects in acid-catalyzed reactions of biomass-derived oxygenates

Abstract

The rates of Brønsted-acid-catalyzed reactions of ethyl tert-butyl ether, tert-butanol, levoglucosan, 1,2-propanediol, fructose, cellobiose, and xylitol were measured in solvent mixtures of water with three polar aprotic cosolvents: γ-valerolactone; 1,4-dioxane; and tetrahydrofuran. As the water content of the solvent environment decreases, reactants with more hydroxyl groups have higher catalytic turnover rates for both hydrolysis and dehydration reactions. We present classical molecular dynamics simulations to explain these solvent effects in terms of three simulation-derived observables: (1) the extent of water enrichment in the local solvent domain of the reactant; (2) the average hydrogen bonding lifetime between water molecules and the reactant; and (3) the fraction of the reactant accessible surface area occupied by hydroxyl groups, all as a function of solvent composition. We develop a model, constituted by linear combinations of these three observables, that predicts experimentally determined rate constants as a function of solvent composition for the entire set of acid-catalyzed reactions.

Graphical abstract: Universal kinetic solvent effects in acid-catalyzed reactions of biomass-derived oxygenates

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
02 Dec. 2017
Accepted
08 Febr. 2018
First published
08 Febr. 2018

Energy Environ. Sci., 2018,11, 617-628

Universal kinetic solvent effects in acid-catalyzed reactions of biomass-derived oxygenates

T. W. Walker, A. K. Chew, H. Li, B. Demir, Z. C. Zhang, G. W. Huber, R. C. Van Lehn and J. A. Dumesic, Energy Environ. Sci., 2018, 11, 617 DOI: 10.1039/C7EE03432F

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