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Quantitative SO(2) Detection in Combustion Environments Using Broad Band Ultraviolet Absorption and Laser-Induced Fluorescence

[Image: see text] Spectrally resolved ultraviolet (UV) absorption cross sections of SO(2) in combustion environments at temperatures from 1120 to 1950 K were measured for the first time in well-controlled conditions through applying broad band UV absorption spectroscopy in specially designed one-dim...

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Detalles Bibliográficos
Autores principales: Weng, Wubin, Aldén, Marcus, Li, Zhongshan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776380/
https://www.ncbi.nlm.nih.gov/pubmed/31364841
http://dx.doi.org/10.1021/acs.analchem.9b02505
Descripción
Sumario:[Image: see text] Spectrally resolved ultraviolet (UV) absorption cross sections of SO(2) in combustion environments at temperatures from 1120 to 1950 K were measured for the first time in well-controlled conditions through applying broad band UV absorption spectroscopy in specially designed one-dimensional laminar flat flames. The temperature was observed to have a significant effect on the absorption cross-section profiles at wavelength shorter than 260 nm, while at the longer wavelength side, the absorption cross-section profiles have much less dependence on temperature. The absorption cross section at 277.8 nm with a value of 0.68 × 10(–18) cm(2)/molecule was suggested for the evaluation of the SO(2) concentration because of the weak dependence on temperature. To make spatially resolved measurements, laser-induced fluorescence (LIF) of SO(2) excited by a 266 nm laser was investigated. Spectrally resolved LIF signal was analyzed at different temperatures. The LIF signal showed strong dependence on temperature, which can potentially be used for temperature measurements. At elevated temperatures, spatially resolved LIF SO(2) detection up to a few ppm sensitivity was achieved. Combining UV broad band absorption spectroscopy and LIF, highly sensitive and spatially resolved quantitative measurements of SO(2) in the combustion environment can be achieved.