The oxidation of a gasoline surrogate in the negative temperature coefficient region
- Department of Mechanical Engineering and Mechanics, Drexel University, 3141 Chestnut Street, Philadelphia, PA 19104-2875 (United States)
- Department of Chemistry, Drexel University, 3141 Chestnut Street, Philadelphia, PA 19104-2875 (United States)
This experimental study investigated the preignition reactivity behavior of a gasoline surrogate in a pressurized flow reactor over the low and intermediate temperature regime (600-800 K) at elevated pressure (8 atm). The surrogate mixture, a volumetric blend of 4.6% 1-pentene, 31.8% toluene, 14.0% n-heptane, and 49.6% 2,2,4-trimethyl-pentane (iso-octane), was shown to reproduce the low and intermediate temperature reactivity of full boiling range fuels in a previous study. Each of the surrogate components were examined individually to identify the major intermediate species in order to improve existing kinetic models, where appropriate, and to provide a basis for examining constituent interactions in the surrogate mixture. n-Heptane and 1-pentene started reacting at 630 K and 640 K, respectively, and both fuels exhibited a strong negative temperature coefficient (NTC) behavior starting at 700 and 710 K, respectively. Iso-octane showed a small level of reactivity at 630 K and a weak NTC behavior starting at 665 K. Neat toluene was unreactive at these temperatures. The surrogate started reacting at 630 K and exhibited a strong NTC behavior starting at 693 K. The extent of fuel consumption varied for each of the surrogate constituents and was related to their general autoignition behavior. Most of the intermediates identified during the surrogate oxidation were species observed during the oxidation of the neat constituents; however, the surrogate mixture did exhibit a significant increase in intermediates associated with iso-octane oxidation, but not from n-heptane. While neat toluene was unreactive at these temperatures, in the mixture it reacted with the radical pool generated by the other surrogate components, forming benzaldehyde, benzene, phenol, and ethyl-benzene. The observed n-heptane, iso-octane, and surrogate oxidation behavior was compared to predictions using existing kinetic models. The n-heptane model reasonably predicted the disappearance of the fuel, but overpredicted the formation of several of the smaller intermediates. The iso-octane model significantly overpredicted the reaction of the fuel and formation of the intermediates. The 1-pentene model reasonably predicted the fuel consumption, but underestimated the importance of radical addition to the double bond. The results of this study provide a critical experimental foundation for the investigation of surrogate mixtures and for validation of kinetic models. (author)
- OSTI ID:
- 21147112
- Journal Information:
- Combustion and Flame, Vol. 156, Issue 3; Other Information: Elsevier Ltd. All rights reserved; ISSN 0010-2180
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
HEPTANE
OCTANE
TOLUENE
OXIDATION
MIXTURES
PHENOL
TEMPERATURE COEFFICIENT
BENZENE
FUEL CONSUMPTION
PENTENES
AUTOIGNITION
BENZALDEHYDE
ACTIVATION ENERGY
VALIDATION
MATHEMATICAL MODELS
TEMPERATURE RANGE 0400-1000 K
PRESSURE RANGE KILO PA
REACTION INTERMEDIATES
Surrogates
Flow reactors