Advancing the C4 low-temperature oxidation chemistry through species measurements in a rapid compression machine. Part B: n-Butane

• Published in: Combustion and flame 2025-02, Vol.272, Article 113861
• Main Authors: Caravaca-Vilchez, Jesus, Liu, Jiaxin, Wang, Pengzhi, Murakami, Yuki, Wu, Yingtao, Curran, Henry J., Heufer, Karl Alexander
• Format: Article
• Language: English
• Subjects: GC-MS/FID system; Ignition delay time; n-butane; Rapid compression machine; Sampling study; Species concentrations
• ISSN: 0010-2180
• DOI: 10.1016/j.combustflame.2024.113861

Studying the oxidation of n-butane, a major component of LNG, is critical to improve the efficiency of transportation engines. Furthermore, its negative temperature coefficient (NTC) behavior provides insights into the oxidation of larger hydrocarbons. Several studies have investigated n-butane oxidation at engine-operating pressures using various methods, including ignition delay time (IDT) measurements in rapid compression machines (RCMs) and shock tubes, flame velocities, and species concentrations in flow reactors. While these species measurements provide deeper insights into oxidation networks than IDTs, they are limited to either low-pressure or highly diluted conditions. To address this gap, this study measures species concentrations during n-butane oxidation at 30 bar in the NTC region (742 K and 855 K, respectively), at stoichiometric and moderate dilution levels in an RCM. A novel two-valve setup allowed gas sample extraction for off-line gas chromatography-mass spectrometry analysis. Complementary IDT data were obtained in the temperature range of 680−910 K, at pressures of 15 and 30 bar, and equivalence ratios of 0.5, 1.0, and 2.0. The results suggest that while current n-butane models reasonably predict its autoignition characteristics, they fall short in predicting the formation of key oxidation intermediates at engine-relevant conditions. In this context, the n-butane submechanism within the NUIGMech1.3 framework was updated. Modifications involve recently computed thermochemical data for critical intermediates and adjustments to rate constants, using analogies with structurally similar molecules such as n-propane and n-pentane. The present model reproduces reasonably well both the measured IDT and species concentrations documented herein and data from the literature. Nevertheless, the model slightly underestimates the reactivity within the NTC domain and the formation of some intermediates at the NTC peak. This study highlights the importance of integrating species concentration and IDT measurements at application-relevant conditions to refine kinetic mechanisms and significantly advances the understanding of C4 hydrocarbon oxidation chemistry. Novelty and Significance Statement The novelty of this research lies in the measurement of species concentrations during the ignition delay of n-butane mixtures in an RCM at high pressures near the NTC minimum and maximum using a novel two-valve gas sampling setup. This, in combination with new therm