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Quantitative Measurement of OH* and CH* Chemiluminescence in Jet Diffusion Flames
Author(s) -
Yao Liu,
Jianguo Tan,
Minggang Wan,
Lang Zhang,
Xiao Yao
Publication year - 2020
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.0c01093
Subject(s) - chemiluminescence , diffusion flame , diffusion , combustion , chemistry , jet (fluid) , flame structure , nozzle , analytical chemistry (journal) , laminar flow , aerosol , methane , optics , mechanics , combustor , physics , thermodynamics , chromatography , organic chemistry
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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