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Oxidation of n-Butane: Transition in the Mechanism across the Region of Negative Temperature Coefficient

机译:正丁烷的氧化:负温度系数区域内机理的转变

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An experimental investigation has been conducted of the transition in the oxidation chemistry of n-butane across the region of negative temperature coefficient from low to intermediate temperatures. The experimental results indicated a region of negative temperature coefficient between approximately 640 and 695 K and a shift in the nature of the reaction intermediates and products across this region. On the basis of these experimental results and some recent kinetic modeling results for the reaction R + O_2 ←→ RO_2, a new mechanism is presented for n-butane to describe the observed phenomena. At low temperatures the major reaction path of butylperoxy is isomerization followed by O_2 addition, further isomerization, and decomposition to mainly carbonyls and OH radicals. At intermediate temperatures, the major reaction of butylperoxy is isomerization followed by decomposition to butenes and HO_2 and to epoxides and OH. The mechanism is consistent with these and other experimental results and predicts the negative temperature coefficient and the shift in product distribution with temperature.
机译:已经进行了实验研究,研究了正丁烷在负温度系数范围内从低温到中间温度的转变过程。实验结果表明,负温度系数的区域介于约640和695 K之间,并且反应中间体和产物的性质在该区域上发生了变化。根据这些实验结果和最近的反应R + O_2←→RO_2的动力学模型结果,提出了一种新的正丁烷机理来描述观察到的现象。在低温下,丁基过氧化物的主要反应路径是异构化,接着是O_2加成,进一步异构化,并分解为主要的羰基和OH基。在中间温度下,丁基过氧基的主要反应是异构化,然后分解为丁烯和HO_2,然后分解为环氧化物和OH。该机理与这些和其他实验结果一致,并预测负温度系数和产物分布随温度的变化。

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