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The critical tube diameter in a two reaction steps detonation: the H2/NO2 mixture case

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Abstract

We present experimental results on the detonability of the H2/NO2 mixture whose detonation exhibits a single cellular structure (λ1) for the lean mixtures and a double cellular structure (fine cells of size λ1 inside larger cells of size λ2) for stoichiometric and rich mixtures. Whatever the equivalence ratio \({\phi}\) , the chemical energy is released in two successive exothermic steps of heat of reaction Q 1 and Q 2 (Q 1 + Q 2 = Q, the total heat release) and characterised (for \({\phi > 1}\)) by two chemical lengths. The detonability is evaluated on the basis of critical conditions of self-sustained detonations transmission from a cylindrical tube of i.d. d to free space. Results show that for the critical tube diameter relationship d1 = k, with respect to the equivalence ratio \({\phi}\) ranging from 0.5 to 1.3 at ambient temperature, k is higher than the classical value 13 and its variation is rather complex. Indeed, d1 increases with \({\phi}\) from 17–18 for \({\phi = 0.5}\) to 45–50 for \({\phi = 1}\) and to 90–100 for \({\phi = 1.3}\) . The highest detonability obtained for \({\phi = 0.6}\) is explained on the basis of the highest relative contribution of the first exothermic step to the total energy Q. We conclude that, as d1 drops with Q 2 decreasing, it should tend to 13 with the vanishing second exothermic reaction.

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Correspondence to D. Desbordes.

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Communicated by L. Bauwens.

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Desbordes, D., Joubert, F., Virot, F. et al. The critical tube diameter in a two reaction steps detonation: the H2/NO2 mixture case. Shock Waves 18, 269–276 (2008). https://doi.org/10.1007/s00193-008-0130-5

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  • DOI: https://doi.org/10.1007/s00193-008-0130-5

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