An experimental and modeling study of ethanol oxidation kinetics in an atmospheric pressure flow reactor

Abstract

Abstract Experimental profiles of stable species concentrations and temperature are reported for the flow reactor oxidation of ethanol at atmospheric pressure, initial temperatures near 1100 K and equivalence ratios of 0.61–1.24. Acetaldehyde, ethene, and methane appear in roughly equal concentrations as major intermediate species under these conditions. A detailed chemical mechanism is validated by comparison with the experimental species profiles. The importance of including all three isomeric forms of the C 2 H 5 O radical in such a mechanism is demonstrated. The primary source of ethene in ethanol oxidation is verified to be the decomposition of the C 2 H 4 OH radical. The agreement between the model and experiment at 1100 K is optimized when the branching ratio of the reactions of C 2 H 5 OH with OH and H is defined by (30% C 2 H 4 OH + 50% CH 3 CHOH + 20% CH 3 CH 2 O) + XH. As in methanol oxidation, HO 2 chemistry is very important, while the H + O 2 chain branching reaction plays only a minor role until late in fuel decay, even at temperatures above 1100 K.