The thermodynamic properties of reactions of aluminum and fluorine compounds in high temperature hydrogen-oxygen flames were determined employing a specially designed four-stage differentially pumped vacuum-mass spectrometer system. Investigation of the chemical equilibria involved established the r
Luminescence from hydrogenfluorine flames, dilute in methane
✍ Scribed by C. Moore; M. Erickson; M. Kaufman
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 592 KB
- Volume
- 87
- Category
- Article
- ISSN
- 0010-2180
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✦ Synopsis
Mechanisms producing luminescence from CH, C 2 , and CHF in CH4-F 2 flames are studied by the method of very dilute flames, whereby small amounts of CH,, (below 2%) are added to H2-F 2 flames. This technique allows the dependence of the emission intensities on the concentration of CH4 and carbon-containing radicals to be separated from its dependence on equivalence ratio and pressure, which determines flame temperature and the concentration of hydrogen and fluorine atoms. The most likely mechanism for C 2 emission is the reaction of two CH radicals, while CH emission (both A and B states) and CHF emission probably result from vibration-to-electronic (V-E) energy transfer from vibrationally excited HF. Experiments using CD 4 and O 2 are in agreement with the mechanism proposed for CH emission. The isotope experiments, as well as laser-induced fluorescence measurements on CH, indicate that the V-E energy transfer is by a single step, rather than by stepwise excitation up the vibrational ladder of CH(X). A diagnostics for the [F]/[F2] ratio in F2-H 2 or F2-hydrocarbon combustion is suggested. The mechanisms proposed for CH and C 2 luminescence are different from those generally discussed for the same emissions in oxygen-supported combustion.
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