A comprehensive experimental and kinetic modeling study of di-isobutylene isomers: Part 1

摘要

Di-isobutylene has received significant attention as a promising fuel blendstock, as it can be synthe-sized via biological routes and is a short-listed molecule from the Co-Optima initiative. Di-isobutylene is also popularly used as an alkene representative in multi-component surrogate models for engine stud-ies of gasoline fuels. However, there is limited experimental data available in the literature for neat di-isobutylene under engine-like conditions. Hence, most existing di-isobutylene models have not been ex-tensively validated, particularly at lower temperatures (< 10 0 0 K). Most gasoline surrogate models in-clude the di-isobutylene sub-mechanism published by Metcalfe et al. [1] with little or no modification. The current study is undertaken to develop a detailed kinetic model for di-isobutylene and validate the model using a wide range of relevant experimental data. Part 1 of this study exclusively focuses on the low-to intermediate temperature kinetics of di-isobutylene. An upcoming part 2 discusses the high -temperature model development and validation of the relevant experimental targets. Ignition delay time measurements for the di-isobutylene isomers were performed at pressures ranging from 15 - 30 bar at equivalence ratios of 0.5, 1.0, and 2.0 diluted in air and in the temperature range 650 - 900 K using two independent rapid compression machine facilities. In addition, measurements of species identified dur-ing the oxidation of these isomers were performed in a jet-stirred reactor and in a rapid compression machine. A detailed kinetic model for the di-isobutylene isomers is developed to capture the wide range of new experimental targets. For the first time, a comprehensive low-temperature chemistry submodel is included. The differences in the important reaction pathways for the accurate prediction of the oxidation of the two DIB isomers are compared using reaction path analysis. The most sensitive reactions control-ling the ignition delay times of the DIB isomers under the pressure and temperature conditions necessary for autoignition in engines are identified.Published by Elsevier Inc. on behalf of The Combustion Institute.