Lanquetin R, Coudert LH, Camy-Peyret C
Unité propre du CNRS (UPR 0136), Université Pierre et Marie Curie, Tour 13, Boîte 76, 4 Place Jussieu, Paris Cedex 05, 75252, France
J Mol Spectrosc. 1999 May;195(1):54-67. doi: 10.1006/jmsp.1999.7822.
Emission spectra of methane-oxygen low-pressure flames have been recorded at a resolution of 0.02 cm-1 with an infrared Fourier transform spectrometer in the spectral ranges 780-1370 and 1800-5000 cm-1. The flame temperature was about 1850 K and a large number of transitions involving J values as high as 34 for an extended set of vibrational states could be assigned. Combined with already published data sets on H2O, our line position analysis yielded rotational energy levels for many of these states, but only the results relevant to the ground and the (010) states are presented here. The experimental energies for these two states have been fitted with the help of the bending-rotation Hamiltonian approach [L. H. Coudert, J. Mol. Spectrosc. 181, 246-273 (1997)], and for each rotational level, the calculated energy along with its uncertainty is reported and compared with the observed value. Comparisons with other available energy level data sets for the ground and (010) states are also presented. Copyright 1999 Academic Press.
利用红外傅里叶变换光谱仪,在780 - 1370和1800 - 5000 cm-1光谱范围内,以0.02 cm-1的分辨率记录了甲烷 - 氧气低压火焰的发射光谱。火焰温度约为1850 K,可以确定涉及一系列扩展振动状态且J值高达34的大量跃迁。结合已发表的关于H2O的数据集,我们的谱线位置分析得出了其中许多状态的转动能级,但这里仅给出与基态和(010)态相关的结果。借助弯曲 - 转动哈密顿方法[L. H. 库德特,《分子光谱学杂志》181, 246 - 273 (1997)]对这两个状态的实验能量进行了拟合,并且对于每个转动能级,报告了计算出的能量及其不确定度,并与观测值进行了比较。还给出了与基态和(010)态的其他可用能级数据集的比较。版权所有1999年学术出版社。