首页> 外文期刊>Combustion and Flame >Measurements of the auto-ignition of n-heptane/toluene mixtures using a rapid compression machine
【24h】

Measurements of the auto-ignition of n-heptane/toluene mixtures using a rapid compression machine

机译:使用快速压缩机测量正庚烷/甲苯混合物的自燃

获取原文
获取原文并翻译 | 示例
           

摘要

Ignition delay times of undiluted stoichiometric n-heptane/toluene mixtures have been measured in a rapid compression machine (RCM) for pure n-heptane and for an increasing concentration of toluene by liquid volume (25-100%) in the mixture, mainly at two different molar densities (150 and 180 mol/ m3). Initial pressures and temperatures were varied respectively in the 0226-0298 bar range and in the 299-352 K range, in order to allow compressed pressures and temperatures respectively in the 7.95-10.38 bar range and in the 710-814 K range. No ignition was observed for pure toluene due most probably to the variation of the final temperature and pressure in the combustion chamber during the very long ignition times of pure toluene at the experimental conditions considered in this work. The ignition delay variation at fixed temperature and the relative variation of the two-stage ignition times are reported. It is shown how the mixture behavior seems to be governed by the n-heptane chemistry for low toluene amount, while an increase of toluene concentration causes longer ignition delay times. Numerical modeling of the experiments with a recent Lawrence Livermore chemical mechanism for surrogate fuels shows that the results agree fairly well in the case of low and mid proportion of toluene by liquid volume. The single-zone model has allowed to extend the temperature range of investigation, showing that the low temperature range is the most influenced by the presence of toluene.
机译:已在快速压缩机(RCM)中测量了纯正庚烷和甲苯浓度随混合物中液体体积的增加(25-100%)而增加时未稀释的化学计量正庚烷/甲苯混合物的点火延迟时间,主要是在两种不同的摩尔密度(150和180 mol / m3)。初始压力和温度分别在0226-0298 bar和299-352 K范围内变化,以便允许压缩压力和温度分别在7.95-10.38 bar和710-814 K范围内变化。在此工作中考虑的实验条件下,纯甲苯的极长点火时间期间,燃烧室中的最终温度和压力发生变化,这极有可能导致纯甲苯未着火。报告了固定温度下的点火延迟变化和两阶段点火时间的相对变化。结果表明,对于低甲苯量来说,混合物的行为似乎受正庚烷化学的支配,而甲苯浓度的增加会导致更长的点火延迟时间。使用最近的劳伦斯·利弗莫尔化学机理进行替代燃料实验的数值模型表明,在甲苯的中低比例(按液体体积计)的情况下,结果相当吻合。单区模型允许扩展研究的温度范围,表明低温范围受甲苯的存在影响最大。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号