Non-premixed ignition of n-heptane and iso-octane in a laminar counterflow

J. D. Blouch, C. K. Law

Research output: Contribution to journalConference article

27 Scopus citations

Abstract

The air temperature needed to ignite a prevaporized fuel/nitrogen mixture in a counterflow was determined experimentally over a range of strain rates and pressures for the reference fuels n-heptane and isooctane. The experiments were modeled with detailed transport and chemistry using semiempirical reaction mechanisms. For both fuels, increasing strain rate increased the ignition temperature, increasing pressure decreased the ignition temperature, and the models overpredicted the ignition temperature by about 100 K. The ignition temperature of n-heptane is lower than that of iso-octane. These results were in qualitative agreement with previous data for C2-C4 hydrocarbons. A comparison of C1 to C8 ignition temperatures revealed the interplay between three main factors. The structure of the fuel molecule and the reactivity of the alkyl radical were responsible for the high ignition temperature for methane, isobutane, and isooctane. The reduced rate of diffusion as the fuel molecule became larger was responsible for an initial increase in ignition temperature for small alkanes. Finally, the general finite-rate kinetic mechanism of hydrocarbon oxidation was responsible for the somewhat uniform ignition temperatures for larger fuels. The change in ignition temperature due to kinetic differences between the fuels was small in light of the uncertainties in measuring the ignition temperatures.

Original languageEnglish (US)
Pages (from-to)1679-1686
Number of pages8
JournalProceedings of the Combustion Institute
Volume28
Issue number2
DOIs
StatePublished - Jan 1 2000
Event30th International Symposium on Combustion - Chicago, IL, United States
Duration: Jul 25 2004Jul 30 2004

All Science Journal Classification (ASJC) codes

  • Chemical Engineering(all)
  • Mechanical Engineering
  • Physical and Theoretical Chemistry

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