The
kinetic effects of n-heptane addition on low
and high temperature oxidations of methane were experimentally investigated
over a range of temperatures from 800 to 1200 K, at the equivalence
ratio of 0.5 in an atmospheric jet-stirred reactor (JSR). The n-heptane content in the methane/n-heptane
mixture was varied between 0 and 100%. The mole fractions of CH4, nC7H16, O2, CO, CO2, CH2O, and C2H4 were determined
respectively in the present experiments, and the NUI mechanism was
employed to perform the numerical studies under the same conditions
by using the perfectly stirred reactor model. The results show that
the onset temperature of the oxidation of methane decreases with the
increase of the n-heptane content in methane/n-heptane mixture significantly, and that even a small amount
of n-heptane can cause an obvious shift of high temperature
oxidation of methane to lower temperature. According to the reaction
path analysis, the initial kinetic enhancement reactions of n-heptane in the oxidation of methane are identified. It
is shown that the kinetic enhancement of methane oxidation by n-heptane addition increases at low temperature. The sensitivity
analysis of the mole fraction of methane indicate that the methane
oxidation is mainly sensitive to those relevant reactions involving
OH, HO2, and other radicals produced by n-heptane at low temperature, and especially at low n-heptane content through the radical pool enrichment. The present
study indicates the potential of n-heptane-assisted
methane combustion in diesel and marine engine applications.