Coherent Stokes Raman Scattering for Simultaneous Measurement of CO2 and CH4 Temperatures

IF 2.2 3区 化学 Q2 SPECTROSCOPY
Journal of Raman Spectroscopy Pub Date : 2026-10-01 Epub Date: 2026-06-10 DOI:10.1002/jrs.70176
Alexander M. Warner, Robert P. Lucht, Rohan M. Gejji, Carson D. Slabaugh
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引用次数: 0

Abstract

Experimental measurements of fuel and flame temperatures in a methane/air co-flow diffusion flame are performed using coherent Stokes Raman scattering. A three-beam hybrid fs/ps configuration is employed such that the excitation bandwidth of the ultrafast pulses includes the rovibrational transitions in the Fermi-dyad of CO 2 and the v 2 mode of CH 4 . Time-domain spectroscopic models were developed and employed to simultaneously extract the CH 4 and CO 2 temperatures separately from the same CSRS spectra. Axial and radial temperature profiles of CH 4 and CO 2 in the diffusion flame are presented. Methane temperatures ranged from 300 to 900 K while CO 2 temperatures ranged from 500 to 2500 K. At probe volume locations higher above the burner, the fuel and product temperatures were in strong agreement. Measurement locations near the methane injector revealed inhomogeneities between fuel and flame temperatures before significant mixing by diffusion. For the first time, a three-beam ultrafast CSRS configuration is demonstrated to simultaneously measure differing CH 4 and CO 2 temperatures.

同步测量CO2和CH4温度的相干斯托克斯拉曼散射
利用相干斯托克斯拉曼散射对甲烷/空气共流扩散火焰中的燃料和火焰温度进行了实验测量。采用三束混合fs/ps结构,使得超快脉冲的激发带宽包括co2费米二极体中的旋转振动跃迁和CH的v2模式4 .建立了时域光谱模型,并利用该模型从同一CSRS光谱中分别提取了ch4和CO 2温度。给出了甲烷和二氧化碳在扩散火焰中的轴向和径向温度分布。甲烷温度范围为300 ~ 900 K, co2温度范围为500 ~ 2500 K。在高于燃烧器的探针体积位置,燃料和产品温度非常一致。甲烷喷射器附近的测量位置揭示了在通过扩散进行显著混合之前燃料和火焰温度之间的不均匀性。首次证明了三束超快CSRS结构可以同时测量不同的ch4和CO 2温度。
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来源期刊
CiteScore
5.40
自引率
8.00%
发文量
185
审稿时长
3.0 months
期刊介绍: The Journal of Raman Spectroscopy is an international journal dedicated to the publication of original research at the cutting edge of all areas of science and technology related to Raman spectroscopy. The journal seeks to be the central forum for documenting the evolution of the broadly-defined field of Raman spectroscopy that includes an increasing number of rapidly developing techniques and an ever-widening array of interdisciplinary applications. Such topics include time-resolved, coherent and non-linear Raman spectroscopies, nanostructure-based surface-enhanced and tip-enhanced Raman spectroscopies of molecules, resonance Raman to investigate the structure-function relationships and dynamics of biological molecules, linear and nonlinear Raman imaging and microscopy, biomedical applications of Raman, theoretical formalism and advances in quantum computational methodology of all forms of Raman scattering, Raman spectroscopy in archaeology and art, advances in remote Raman sensing and industrial applications, and Raman optical activity of all classes of chiral molecules.
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