Quantitative Measurement of OH and CH Chemiluminescence in Jet Diffusion Flames

Quantitative measurement of chemiluminescence is a challenging work that limits the development of combustion diagnostics based on chemiluminescence. Here, we present a feasible method to obtain effective quantitative chemiluminescence data with an integrating sphere uniform light source. Spatial di...

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Bibliographic Details
Published inACS omega Vol. 5; no. 26; pp. 15922 - 15930
Main Authors Liu, Yao, Tan, Jianguo, Wan, Minggang, Zhang, Lang, Yao, Xiao
Format Journal Article
LanguageEnglish
Published American Chemical Society 07.07.2020
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Summary:Quantitative measurement of chemiluminescence is a challenging work that limits the development of combustion diagnostics based on chemiluminescence. Here, we present a feasible method to obtain effective quantitative chemiluminescence data with an integrating sphere uniform light source. Spatial distribution images of OH* and CH* radiation from methane laminar diffusion flames were acquired using intensified charge-coupled device (CCD) cameras coupled with multiple lenses and narrow-band-pass filters. After the process of eliminating background emissions by three filters and the Abel inverse transformation, the chemiluminescence intensity was converted to a radiating rate based on the uniform light source. The simulated distributions of OH* and CH* agree well with the experimental results. It has also been found that the distribution of OH* is more extensive and closer to the flame front than that of CH*, demonstrating that OH* is more representative of the flame structure. Based on the change in the reaction rate of different formation reactions, OH* distributions can be divided into three regions: intense section near the nozzle, transition section in the middle of the flame, and secondary section downstream the flame, whereas CH* only exists in the first two regions. In addition, as the velocity ratio of methane and co-flowing air increases, the main reactions become more intense, while the secondary reaction of OH* becomes weaker.
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ISSN:2470-1343
2470-1343
DOI:10.1021/acsomega.0c01093