4.7 Article

Autoignition of DME/H2 mixtures in a rapid compression machine under low-to-medium temperature ranges

期刊

FUEL
卷 194, 期 -, 页码 50-62

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2016.12.096

关键词

Ignition delays; DME; Hydrogen; Rapid compression machine

资金

  1. Projects of International Cooperation and Exchanges NSFC [51611130193]
  2. National Natural Science Foundation of China [51376011]
  3. Beijing Natural Science Foundation Program [3152005]
  4. Scientific Research Key Program of Beijing Municipal Commission of Education [KZ201410005003]
  5. Project of Fourteenth Scientific Research Foundation for Graduate Students in Beijing University of Technology [ykj-2015-12159]

向作者/读者索取更多资源

Ignition delays of dimethyl ether and hydrogen (DME/H-2) mixtures (hydrogen blending ratio ranging from 0% to 60%) were measured in a rapid compression machine at compressed temperatures ranging from 655 to 810 K and compressed pressures from 16.9 to 24.5 bar with an equivalence ratio range of 0.8-1.6. Experimental measurements are compared with results from numerical simulations using the NUIG Mech_56.54 mechanism and, in general, a good agreement is obtained. The first-stage ignition delay of DME/H2 mixtures proves to be insensitive to compressed pressure and equivalence ratio, whereas the total ignition delay decreases distinctly with the increase of compressed pressure and equivalence ratio, especially in the negative temperature coefficient (NTC) region. Moreover, the simulation results show that the NTC region shifts to a higher temperature when compressed pressure is increased. Increasing the equivalence ratio enhances the overall system reactivity but does not significantly change the temperature range of the NTC region. Both first-stage and total ignition delay increase with the increase of hydrogen blending ratio. The total ignition delay as a function of hydrogen blending ratio increases nonlinearly, and the effect of hydrogen addition becomes more prominent in the NTC region and at 60% hydrogen blending ratio. Kinetic analysis indicates that hydrogen addition consumes OH radical and inhibits DME low-temperature oxidation. More fuel molecules undergo chain propagation reaction subsequently, leading to the decrease of heat release and radicals generated during the first-stage ignition and longer total ignition delay. (C) 2016 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据