Pathways, kinetics and thermochemistry of methyl-ester peroxy radical decomposition in the low-temperature oxidation of methyl butanoate: A computational study of a biodiesel fuel surrogate

A chemical kinetic submechanism proposed here is an essential prerequisite to model autoignition of methyl esters at low temperature region (less than similar to 900 K), where reactions of methyl-ester peroxy radicals (ROO center dot) and hydroperoxy methyl-ester radicals (Q(center dot)OOH) are crucial and relatively unexplored. The potential energy surfaces of the methyl butanoate peroxy radicals + O-2 systems are computed by the G3MP2B3 composite approach. 114 pathways are identified leading to the formation of key radicals in the ignition kernel such as OH and HO2. Particular attention is focused on: (1) intramolecular H-migration of ROO center dot (2) unimolecular dissociations of ROO center dot and Q(center dot)OOH and (3) reactions of ROO center dot + HO2. Using the canonical transition state theory, the high-pressure limit rate constants for reactions in the kinetic submechanism are calculated. Standard enthalpy of formation, entropy and heat capacities are evaluated for intermediates and products formed during combustion by means of the standard statistical mechanics formulae. The agreement and disagreement between our calculated kinetic parameters and previous estimates offer further insight into the uncertainty associated with theoretical estimation. We perform the branching ratio analysis for the competing channels between the reverse dissociation of ROO center dot (ROO center dot -> R + O-2) and explored unimolecular reactions decomposing ROO center dot. Additionally, we also quantify the similarity and dissimilarity between the rate constants determined here and those previously calculated for normal alkanes. Finally, the effect of transition state size on the rate constants for the isomerizations of methyl-ester peroxy radicals is systematically analyzed. (C) 2014 The Combustion Institute. Published by Elsevier Inc. All rights reserved.