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Temperature Measurements of Shock Waves and Detonations by Spectrum-Line Reversal. III. Observations with Chromium Lines
A. G. Gaydon and I. R. Hurle
Proceedings of the Royal Society of London. Series A, Mathematical and Physical Sciences
Vol. 262, No. 1308 (Jun. 13, 1961), pp. 38-50
Published by: Royal Society
Stable URL: http://www.jstor.org/stable/2414087
Page Count: 15
You can always find the topics here!Topics: Chromium, Detonation, Argon, Shock waves, Sodium, Temperature measurement, High temperature, Carbon monoxide, Thermodynamic equilibrium, Shock fronts
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Temperature measurements have been made with the chromium resonance triplet at 4254, 4274 and 4289 Å, controlled amounts of chromium being introduced in the form of the volatile carbonyl; this method has the advantage that it can be used with explosive mixtures. Measurements of vibrational relaxation time have been made for carbon monoxide between 2200 and 2700 ⚬K and of the rate of dissociation of hydrogen in hydrogen+argon mixtures between 2400 and 2800 ⚬K. Temperature irregularities in the fronts of shocks through argon or neon are discussed, but no satisfactory explanation for them has been found. Excitation processes in monatomic gases are also examined. The method has been used to study the temperature distribution behind detonations which have been initiated by shocks of various strengths. For ethylene+oxygen detonations the chromium excitation temperature is very high at the front; this is attributed to chemilummescent excitation in the reaction zone. In carbon monoxide+oxygen detonations initiated by weak shock waves we have observed interesting steps in the temperature behind the front and have explained these as being due to delayed ignition behind the shock and an acceleration of the front leading to detonation after the front has travelled some way along the shock tube.
Proceedings of the Royal Society of London. Series A, Mathematical and Physical Sciences © 1961 Royal Society