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Application of frequency modulation spectroscopy to shock tube studies of elementary amidogen reactions.

机译:调频光谱在激波管中研究基本酰胺原反应的应用。

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The reaction of NH2 with NO plays an important role in the Thermal De-NOx process and reburning. In the Thermal De-NOx process, NO2 is an important intermediate, and the NH2 + NO 2 reaction plays a key role in recycling NO2 back to NO and in N2O formation. While there are multiple pathways for both reactions, leading to different products, only two product channels for each reaction are dominant: NH2+NO=NNH+OH R1a NH2+NO=N2+H2O R1b NH2+NO2=N2O+H 2OR2a NH2+NO2=H2NO+NO R2b ; In the present study, the overall rate coefficients (k1 = k1a + k1b, k2 = k2a + k2b ) and branching ratios (α1 = k1a/k 1, α2 = k2a/k2) of the NH 2 + NO and NH2 + NO2 reactions have been determined using a shock tube facility and frequency modulation spectroscopy of NH 2.; Using the frequency modulation absorption technique, a significant improvement in NH2 detection can be achieved. An equivalent absorption detection limit of 0.01% and 0.003% was achieved for non-resonant and resonant type electro-optic modulators, respectively. Due to the sensitive detection of NH2 radicals, the initial concentration of the reactants can be lowered and consequently the influence of secondary reactions is reduced.; For high temperature experiments to determine k1, NH 2 radicals were produced by thermal decomposition of monomethylamine, CH3NH2 (MMA). For the low temperature experiments, benzylamine, C6H5CH2NH2 (BA) was used as a source of NH2. The measured NH2 traces were interpreted using a detailed reaction mechanism. The MMA and BA data are consistent with lower temperature data from other studies.; To obtain the branching ratio, α1, NH2 radicals were produced by photolysis of NH3 at low temperatures (1700K) and pyrolysis of BA at high temperatures (>1800K). In excess NH3, the NH2 trace was mainly sensitive to the branching ratio. The measured branching ratios increased from 0.40 at 1340K to 0.66 at 2159K, and were in good agreement with results of the theoretical work.; For experiments on reaction R2a and R2b, BA was used as a thermal source of NH2 radicals. The IR emission from N2O was monitored to determine the branching ratio, α2. The measured α 2-value was 0.17 ± 0.04 for the temperature range 1319–1493K, which is consistent with the results of lower temperature studies.
机译:NH 2 与NO的反应在热脱硝过程和再燃烧中起重要作用。在热脱硝工艺中,NO 2 是重要的中间产物,NH 2 + NO 2 反应在循环利用中起关键作用NO 2 还原为NO,并形成N 2 O。虽然两种反应都有多种途径,导致产物不同,但每个反应只有两个产物通道占主导: NH 2 + NO = > NNH + OH R1a NH 2 + NO => N 2 + H 2 O R1b NH 2 + NO 2 => N 2 < / inf> O + H 2 O R2a NH 2 + NO 2 => H 2 NO + NO < fen lp =“ par”> R2b ;在本研究中,总体速率系数(k 1 = k 1a + k 1b ,k 2 = k 2a + k 2b )和分支比率(α 1 = k 1a / k 1 < / sub>,α 2 = k 2a / k 2 )的NH 2 + NO和NH <使用冲击管设备和NH 2 的频率调制光谱确定了sub> 2 + NO 2 反应。使用调频吸收技术,可以大大改善NH 2 的检测。非谐振型和谐振型电光调制器的等效吸收检测极限分别达到0.01%和0.003%。由于可以灵敏地检测到NH 2 自由基,因此可以降低反应物的初始浓度,从而降低了副反应的影响。为了测定k 1 的高温实验,通过单甲胺CH 3 NH 2 的热分解产生了NH 2 自由基。 sub>(MMA)。在低温实验中,使用苄胺,C 6 H 5 CH 2 NH 2 (BA)作为NH 2 的来源。使用详细的反应机理解释了测得的NH 2 痕量。 MMA和BA数据与其他研究的较低温度数据一致。为了获得支化比,通过在低温(<1700K)下对NH 3 进行光解和对NH 3 的热解来生成α 1 ,NH 2 自由基。 BA在高温(> 1800K)下。过量的NH 3 中,NH 2 的痕迹主要对支化比敏感。测得的支化比从1340K的0.40增加到2159K的0.66,与理论工作结果吻合良好。在反应R2a和R2b的实验中,BA被用作NH 2 自由基的热源。监测N 2 O的红外发射以确定支化比α 2 。在1319–1493K的温度范围内测得的α 2 值为0.17±0.04,与较低温度研究的结果一致。

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