2013

An experimental and modeling study of the autoignition of 3-methylheptane

An experimental and modeling study of the autoignition of 3-methylheptane
W. Wang, Z. Li, M. Oehlschlaeger, D.Healy, H. Curran, M. Sarathy, M. Mehl, W. Pitz, C. Westbrook
Proceedings of the Combustion Institute,  34 (1),  335–343 (2013)
W. Wang, Z. Li, M. Oehlschlaeger, D.Healy, H. Curran, M. Sarathy, M. Mehl, W. Pitz, C. Westbrook
3-Methylheptane; Shock tube; Rapid compression machine; Chemical kinetic modeling
2013
An experimental and kinetic modeling study of the autoignition of 3-methylheptane, a compound representative of the high molecular weight lightly branched alkanes found in large quantities in conventional and synthetic aviation kerosene and diesel fuels, is reported. Shock tube and rapid compression machine ignition delay time measurements are reported over a wide range of conditions of relevance to combustion engine applications: temperatures from 678 to 1356 K; pressures of 6.5, 10, 20, and 50 atm; and equivalence ratios of 0.5, 1.0, and 2.0. The wide range of temperatures examined provides observation of autoignition in three reactivity regimes, including the negative temperature coefficient (NTC) regime characteristic of paraffinic fuels. Comparisons made between the current ignition delay measurements for 3-methylheptane and previous results for n-octane and 2-methylheptane quantifies the influence of a single methyl substitution and its location on the reactivity of alkanes. It is found that the three C8 alkane isomers have indistinguishable high-temperature ignition delay but their ignition delay times deviate in the NTC and low-temperature regimes in correlation with their research octane numbers. The experimental results are compared with the predictions of a proposed kinetic model that includes both high- and low-temperature oxidation chemistry. The model mechanistically explains the differences in reactivity for n-octane, 2-methylheptane, and 3-methylheptane in the NTC through the influence of the methyl substitution on the rates of isomerization reactions in the low-temperature chain branching pathway, that ultimately leads to ketohydroperoxide species, and the competition between low-temperature chain branching and the formation of cyclic ethers, in a chain propagating pathway.