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Temperature and pressure effects on formationand decomposition of phenylvinylperoxy radicalsin the C6H5C2H2+O2 reaction

机译:C6H5C2H2 + O 2反应中苯基乙烯基哌糖基的形成和分解的温度和压力影响

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The effects of temperature and pressure on the formation and decomposition of C6H5C2H2O2 in the C6H5C2H2+O2 reaction have been investigated at temperatures from 298 to 378 K by directly monitoring the C6H5C2H2O2 radical in the visible region by cavity ringdown spectrometry (CRDS). The rate constant for the C6H5C2H2+O2 association and that for fragmentation of C6H5C2H2O2 were found to be k1 (C6H5C2H2+O2 → C6H5C2H2O2) = (3.20 ± 1.19) ×1011 exp(+760/T) cm3 mol-1 s-1 and k2 (C6H5C2H2 O2 → C6H5CHO + HCO) = (1.68 ± 0.13) ×104 s-1, respectively. Additional kinetic measurements by pulsed laser photolysis/mass spectrometry show that C6H5CHO was produced in the C6H5C2H2+O2 reaction as predicted and the formation of C6H5CHO from the decomposition of C6H5C2H2O2 is temperatureindependent, consistent with the CRDS experimental data.
机译:通过直接监测在可见区域中的C6H5C2H2O2的温度下,通过腔振荡光谱法(CRDS)在从298至378k的温度下研究了温度和压力对C6H5C2H2H2O2的形成和分解C6H5C2H2O2反应的影响。发现C6H5C2H2 + O2关联的速率常数以及C6H5C2H2O2的破碎化为K1(C6​​H5C2H2 + O 2→C6H5C2H2O2)=(3.20±1.19)×1011 exp(+ 760 / T)CM3 mol-1 S-1和K2(C6H5C2H2 O2→C6H5CHO + HCO)=(1.68±0.13)×104s-1。通过脉冲激光光解/质谱法的额外动力学测量表明,在C6H5C2H2 + O 2中产生C6H5CHO,如预测的那样,从C6H5C2H2O2的分解中形成C6H5ChO是温度的,与CRD实验数据一致。

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