Abstract

ABSTRACT Time-resolved quantitative measurements of hydrogen peroxide (H2O2) in the low-temperature oxidation of iso-octane in a rapid compression machine have been performed using mid-infrared absorption spectroscopy. H2O2 was detected in the 8-μm region, wherein H2O2 has the strongest absorption band. Owing to the weak interference of the absorption of iso-octane and H2O in the 8-μm region, H2O and iso-octane were detected in the 1.4- and 3.5-μm region, respectively. The cross-sections of H2O2 and H2O were calculated using parameters in the HITRAN database, and the iso-octane cross-section was measured using a rapid compression machine in the temperature and pressure ranges of 417–700 K and 100–700 kPa, respectively. The time-resolved quantitative H2O2 profiles in the low-temperature oxidation of iso-octane at 0.77 MPa, 642 and 660 K, and an equivalence ratio of 1.0 were successfully obtained. The H2O and iso-octane profiles were also obtained using this measurement method; the simultaneous measurements of the quantitative time profiles of multi-species in the low-temperature oxidation of fuels are also novel. Under experimental conditions, H2O2 was formed during the low-temperature oxidation of iso-octane, and its concentration gradually increased between the end of the low-temperature oxidation and start of the high-temperature oxidation. The calculated H2O2 profiles obtained using the latest chemical kinetic model of iso-octane showed the same tendency as the experimental profiles.

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