An experimental and kinetic modeling study on low-temperature oxidation of gasoline and diesel/polyoxymethylene dimethyl ether (OME3) blends

被引:1
|
作者
Chen, Yong [1 ]
Zhong, Xin [1 ]
Wang, Hu [1 ]
Li, Bing [1 ]
Yao, Zhifeng [1 ]
Zhang, Mengnan [1 ]
Zheng, Zunqing [1 ]
Yao, Mingfa [1 ]
机构
[1] Tianjin Univ, State Key Lab Engines, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Diesel surrogate; Gasoline surrogate; Polyoxymethylene dimethyl ether; Low-temperature oxidation; Chemical kinetic model; IGNITION DELAY TIMES; SHOCK-TUBE; EMISSION CHARACTERISTICS; COMBUSTION; PYROLYSIS; MECHANISM; TOLUENE; FLAMES; DIMETHOXYMETHANE; AUTOIGNITION;
D O I
10.1016/j.combustflame.2023.112902
中图分类号
O414.1 [热力学];
学科分类号
摘要
In this work, the low-temperature oxidation of polyoxymethylene dimethyl ether (OME3) with multi-component surrogates for diesel (DS:60%n-heptane/20%cyclohexane/20%toluene) and gasoline (GS:20%n-heptane/60%iso-octane/20%toluene) blends was investigated respectively using a jet-stirred reactor (JSR) with a temperature range of 500-950 K, constant fuel fraction of 0.008, residence time (& tau;) of 2 s and near atmospheric pressure. Two detailed multi-component kinetic mechanisms were established to de-scribe the low-temperature oxidation characteristics and the interaction of blended fuels. Generally, the oxidation process of highly-reactive OME3 and n-heptane is inhibited, while that of inactive fuels, includ-ing iso-octane, cyclohexane and toluene, are triggered and enhanced in various degrees in the blends. The OH radical acts as a bridge between high and low reactivity components. It is of interest that n-heptane reveals a quite different low-temperature oxidation behavior in diesel (DS) and gasoline (GS) surrogate respectively. In GS, the low-temperature oxidation of n-heptane is significantly inhibited, while in DS, the inhibition is mild, mainly due to the much different low-temperature oxidation character-istics of iso-octane and cyclohexane. As for OME3, it mainly improves the reactivity of the blends in the negative temperature coefficient (NTC) process. As for low-reactivity fuels of iso-octane and toluene, their low-temperature oxidations are completely triggered and dominated by highly-reactive fuels due to their weak OH build-up ability. On the contrary, when the low-temperature oxidation of cyclohexane is triggered, its self-enhancement also plays a crucial role in addition to the promoting effect from highly-reactive fuels. Therefore, cyclohexane reveals a promoting-ignition effect on the blended fuels, while iso-octane and toluene act as an inhibiting-ignition factor in blends.& COPY; 2023 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
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页数:15
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