...
首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Shock Wave Study on the Thermal Unimolecular Decomposition of Allyl Radicals
【24h】

Shock Wave Study on the Thermal Unimolecular Decomposition of Allyl Radicals

机译:烯丙基自由基热单分子分解的冲击波研究

获取原文
获取原文并翻译 | 示例
           

摘要

We present the first direct study on the thermal unimolecular decomposition of allyl radicals.Experiments have been performed behind shock waves,and the experimental conditions covered temperatures ranging from 1125 K up to 1570 K and pressures between 0.25 and 4.5 bar.Allyl radicals have been generated by thermal decomposition of allyl iodide,and H-atom resonance absorption spectroscopy has been used to monitor the reaction progress.A marked pressure dependence of the rate constant has been observed which is in agreement with the results from a master equation analysis.However,our experimental results as well as our Rice-Ramsperger-Kassel-Marcus calculations seem to contradict the results of Deyerl et al.(J.Chem.Phys.1999,110,1450) who investigated the unimolecular decomposition of allyl radicals upon photoexcitation and tried to deduce specific rate constants for the unimolecular dissociation in the electronic ground state.At pressures around 1 bar we extracted the following rate equation:k(T) = 5.3 x 10~(79)(T/K)~(-19.29) exp[(-398.9 kJ/mol)/RT] s~(-1).The uncertainty of the rate constant calculated from this equation is estimated to be 30%.
机译:我们对烯丙基自由基的热单分子分解进行了首次直接研究。在冲击波后进行了实验,实验条件涵盖温度从1125 K到1570 K以及0.25至4.5 bar的压力。已生成烯丙基通过烯丙基碘的热分解和H原子共振吸收光谱法来监测反应进程。已观察到速率常数与压力的显着相关性与主方程分析的结果相符。实验结果以及我们的Rice-Ramsperger-Kassel-Marcus计算似乎与Deyerl等(J.Chem.Phys.1999,110,1450)的结果相矛盾,后者研究了光激发下烯丙基自由基的单分子分解并试图推导电子基态下单分子解离的比速率常数。在大约1 bar的压力下,我们提取了以下速率方程比率:k(T)= 5.3 x 10〜(79)(T / K)〜(-19.29)exp [(-398.9 kJ / mol)/ RT] s〜(-1)。计算出的速率常数的不确定性根据此等式估计为30%。

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