Mixing Laws and Chemical Reaction Mechanisms for Predicting the LBV of CH4/CSC Gases Premixed Flame

IF 1.6 4区 化学 Q4 CHEMISTRY, PHYSICAL
Yu Liu, Mengmeng Luo, Xiaoxiao Chen, Wen Zeng, Fuchao Tian, Yuntao Liang
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Abstract

Coal spontaneous combustion (CSC) process releases a large number of combustible gases, which bring threat to the combustion and explosion of mine methane (CH4). Under the action of CSC, the combustion characteristics of CH4 will undergo significant changes. In the current work, the laminar burning velocity (LBV) of CH4/CSC gases mixed flame was obtained in a constant volume chamber (CVC) under an initial pressure of 0.1 MPa and an initial temperature of 300 K over a wide equivalence ratio range of 0.7–1.3 with three kinds of CSC gases mixing ratios. The effects of CSC gases addition on the LBV of CH4 were analyzed first. And then, four kinds of mixing laws were used to predict the LBV of CH4/CSC gases mixed flame. In addition, six kinds of detailed reaction mechanisms were used to calculate the LBV of CH4/CSC gases mixed flame. Results show that the mixing of all kinds of CSC gases increases the LBV of CH4, and T mixing law is more suitable for predicting the LBV of CH4 mixed with CSC gases in the second stage, while the modified and simplified USC 2.0 mechanism can predict the LBV of CH4 mixed with CSC gases well in all three stages.

预测CH4/CSC气体预混火焰LBV的混合规律和化学反应机理
煤自燃过程释放出大量可燃气体,对矿井甲烷燃烧爆炸造成威胁。在CSC的作用下,CH4的燃烧特性会发生明显的变化。本文在定容室(CVC)中,在初始压力为0.1 MPa、初始温度为300 K、等温比为0.7 ~ 1.3、三种CSC气体混合比的条件下,获得了CH4/CSC气体混合火焰的层流燃烧速度(LBV)。首先分析了CSC气体加入对CH4 LBV的影响。然后,采用四种混合规律预测了CH4/CSC气体混合火焰的LBV。此外,采用6种详细的反应机理计算了CH4/CSC气体混合火焰的LBV。结果表明:各种CSC气体的混合均使CH4的LBV增大,其中T混合定律更适合于预测第二阶段CH4与CSC气体混合的LBV,而改进简化的USC 2.0机制可以很好地预测CH4与CSC气体混合的三个阶段的LBV。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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