Following
stringent regulations enforced by environmental regulatory
authorities, various steps have been recently implemented to ensure
the clean combustion of gasoline with minimum emissions by including
additives to gasoline. This kinetic and experimental study has been
conducted to explore the effect of H2 and CO addition to
Halterman gasoline at stoichiometric conditions of 358 K and 1 bar.
Two different mechanisms, a gasoline surrogate (iso-octane, n-heptane, toluene, and ethanol), LLNL,
and a KAUST TPRFE (primary reference fuel, toluene, and ethanol),
were used to provide a detailed comparative kinetic understanding
of gasoline. Via a spherical flame propagating in a constant-volume
combustion chamber, the unstretched, adiabatic laminar burning velocity, S
L
o, was measured. H2 and CO were added (as unitary and binary
additives) to the Haltermann gasoline, in proportions of 1, 2.5, 5,
and 10% by mass. Adding hydrogen enhanced the S
L
o significantly,
while CO addition had only a slight effect on S
L
o. The maximal mole
fractions of OH and H were increased with the H2 addition,
while adding CO raised the O radical peak mole fraction. A strong
correlation between S
L
o and the sum of the O, H, and OH peak
mole fractions was evident. The OH radical was identified to be a
kinetics indicator for S
L
o of gasoline/air mixtures at these conditions;
a higher fraction of ethanol in Haltermann gasoline was the precursor
for high OH concentration. The addition of a binary additive (10%
H2–10% CO) significantly enhanced the consumption
of iso-octane compared to other fuel species, strengthening
the H-abstraction of iso-octane, 99% compared to
71% with neat Haltermann gasoline. The simulated flame speed showed
that the primary chain branching reaction (H + O2 = O +
OH) rate was much higher for the LLNL mechanism than for the KAUST-TPRFE
mechanism, and thus, the LLNL overpredicted S
L
o for the Haltermann
gasoline surrogate.