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Experimental Measurement of Ignition Delay Times of Thermally Cracked n-Decane in a Shock Tube

机译:冲击管中热裂化正癸烷点火延迟时间的实验测量

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摘要

The ignition characteristics of endothermic hydrocarbon fuels (with different pyrolysis degrees) were investigated in a shock tube using n-decane as model compound. Six component surrogates (CH4/C2H4/C2H6/C3H6/C3H8-C10H22, marked as cracked n-decane) for thermally cracked n-decane were proposed based on the chemical compositions from the thermal stressing of n-decane on electrically heated tube under 5 MPa. Ignition delay times were measured behind reflected shock waves over a temperature range of 1296-1915 K, a pressure of 0.1-0.2 MPa, and equivalence ratios of 0.5-2.0. n-Decane showed a shorter ignition delay time than cracking gas at 0.1 MPa, demonstrating higher reactivity. For cracked n-decane, it was found that thermal cracking could improve the ignitability under certain conditions to a limited degree, i.e., at T > 1480 K for x = 37.97% and x = 17.61% and at T < 1480 K for x = 62.15% (x represents the conversion of thermal cracking of n-decane) in this work. Unimolecular decomposition reactions of n-decane producing active radicals and H atom would help chain initiation via H -abstraction reaction for unreacted fuels. This initial stage might accelerate ignition by activating cracking gas at these conditions. The empirical correlations for the ignition delay time of cracking gas and n-decane were also analyzed and compared with previous works. Two models were also used to simulate the experimental data of n-decane and cracking gas and showed good agreement with experimental results, and a combined model was utilized to predict results of cracked n-decane.
机译:在以正癸烷为模型化合物的激波管中研究了具有不同热解度的吸热烃类燃料的着火特性。根据电加热管上正癸烷的热应力,根据化学成分,提出了用于热裂解正癸烷的六种替代物(CH4 / C2H4 / C2H6 / C3H6 / C3H8 / n-C10H22,标记为裂解正癸烷) 5 MPa以下。在1296-1915 K的温度范围,0.1-0.2 MPa的压力和0.5-2.0的当量比的反射冲击波后面测量点火延迟时间。正癸烷在0.1 MPa时比裂解气显示出更短的点火延迟时间,表明其反应活性更高。对于裂解的正癸烷,发现在一定条件下热裂解可以在一定程度上改善可燃性,即在T> 1480 K时x = 37.97%和x = 17.61%,在T <1480 K时x =在这项工作中,为62.15%(x代表正癸烷的热裂解转化率)。生成正癸烷的活性自由基和H原子的单分子分解反应将有助于通过H-吸收反应对未反应的燃料进行链引发。在这些条件下,此初始阶段可能会通过活化裂解气来加速点火。还分析了裂解气和正癸烷点火延迟时间的经验相关性,并将其与以前的工作进行了比较。还使用两个模型来模拟正癸烷和裂化气的实验数据,并与实验结果显示出良好的一致性,并且使用组合模型来预测裂化正癸烷的结果。

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  • 来源
    《Energy & fuels》 |2017年第3期|3262-3269|共8页
  • 作者单位

    Tianjin Univ, Minist Educ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Tianjin 300072, Peoples R China;

    Tianjin Univ, Minist Educ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Tianjin 300072, Peoples R China;

    Tianjin Univ, Minist Educ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Tianjin 300072, Peoples R China|Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China;

    Tsinghua Univ, Sch Aerosp Engn, Beijing 100084, Peoples R China;

    Tianjin Univ, Minist Educ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Tianjin 300072, Peoples R China|Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
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  • 正文语种 eng
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