NH2和NH自由基的热分解

J. Deppe, G. Friedrichs, A. Ibrahim, H.-J. Römming, H. Gg. Wagner
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引用次数: 24

摘要

在较宽的温度范围内研究了肼热分解过程中NH2和NH自由基以及H和N原子的形成。首次将调频光谱技术应用于激波后NH2自由基的检测。与双光束激光吸收技术相比,检测限提高了1.5个数量级。反应(5)氨基+ M→NH + H + M的速率常数得到温度范围从2200年到4000年Kk5a =(1.2±0.5)1015·exp(-(318±10)kJ摩尔−1 / RT)立方厘米/摩尔砂反应(6)NH + M→N + H + M的温度范围从2500年到3400年Kk6 =(1.8±0.8)1014·exp(-(313±15)kJ摩尔−1 / RT)立方厘米/摩尔颇具实验活化能明显被发现是在良好的协议与理论计算和最近推荐的生成焓变氨基和北半球。NH2分解竞争通道(5b) NH2 + M→N + H2 + M的重要性较低(≤5%)。比较了NH2与H20和3CH2的单分子分解动力学行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Thermal Decomposition of NH2 and NH Radicals

The formation of NH2 and NH radicals as well as H and N atoms during the thermal decomposition of hydrazine was investigated over a wide temperature range. For the first time frequency-modulated spectroscopy was used for the detection of NH2 radicals behind shock waves. In comparison with the dual beam laser absorption technique, the detection limit has been improved by one and a half orders of magnitude.

For reaction (5a) NH2 + M → NH + H + M the rate constants were obtained in the temperature range from 2200 to 4000 K

k5a = (1.2 ± 0.5)1015 · exp[-(318±10) kJ mol−1/RT] cm3/mol s

and for reaction (6) NH + M → N + H + M in the temperature range from 2500 to 3400 K

k6 = (1.8 ± 0.8)1014 · exp[-(313 ± 15)kJ mol−1/RT] cm3/mol s.

The experimental apparent activation energies were found to be in good agreement with theoretical calculations and recently recommended enthalpies of formation for NH2 and NH. The competing NH2 decomposition channel (5b) NH2 + M → N + H2 + M was shown to be of minor importance (⩽ 5%). The kinetic behavior of the unimolecular decomposition of NH2 is compared with that of H20 and 3CH2.

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