Hot surface ignition of n-hexane in air

Abstract

An experimental investigation is conducted to analyze hot-surface ignition of n-hexane-air mixtures. The experimental setup, equipped with temperature diagnostics and schlieren imaging, utilizes a glow plug to initiate ignition in a flammable mixture. The hot-surface temperature at the point of ignition is measured for equivalence ratios ranging from 0.6 to 3 and chamber pressures varying from 25 to 100 kPa. The hot-surface temperature resulting in ignition is found to be weakly sensitive to equivalence ratio with a mean value of 980 K for mixtures with equivalence ratios between 0.75 and 3 at 100 kPa. Chamber pressure has a stronger influence with ignition temperature increasing to about 1140 K at 25 kPa. The experimental trends were reproduced in numerical simulations utilizing detailed chemistry of n-heptane as a surrogate for n-hexane given their similar ignition and flame propagation characteristics. The simulations further predict a two-stage ignition process resulting from an initial breakdown of the fuel with a small increase in temperature followed by a main ignition event accompanied by fuel depletion. Reaction rate analysis of the sequence of events leading to ignition conducted using a reduced order kinetic model suggests that the second-stage ignition event is caused primarily by the decomposition of hydrogen peroxide which occurs at temperatures above 900 K. The two-stage ignition process observed here is significantly different from that observed in previous studies due to the presence of convective and diffusive processes as well as the continuous increase in hot-surface temperature. These arguments are used to explain the insensitivity of ignition temperature to equivalence ratio, its decrease with increasing chamber pressure, and the location of the ignition kernel observed in experiments and simulations.

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