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Journal ArticleDOI

Dynamic Parameters of Gaseous Detonations

John H.S. Lee
- 01 Jan 1984 - 
- Vol. 16, Iss: 1, pp 311-336
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TLDR
In this paper, the authors considered homogeneous gaseous fuel-air detonations and showed that the propagation of the combustion wave is governed by the molecular diffusion of heat and mass from the reaction zone to the unburned mixture, and that the very strong exponential temperature dependence of chemical reaction rates makes possible the rapid combustion in the detonation mode.
Abstract
In addition to gases, flammable liquids and solids in the form of fine droplets and dust particles also form explosive mixtures with air. An explosive mixture can, in general, support two modes of combustion. The slow laminar deflagration mode is at one extreme; here the flame propagates at typical velocities of the order 1 m s -1 relative to the unburned gases and there is negligible overpressure development when the explosion is unconfined. At the other extreme is the detonation mode, in which the detonation wave propagates at about 2000 m s -1 accompanied by an overpressure rise of about 20 bars across the wave. The propagation of laminar defiagrations is governed by the molecular diffusion of heat and mass from the reaction zone to the unburned mixture. The propagation of detonations depends on the adiabatic shock compression of the unburned mixtures to elevated temperatures to bring about autoignition. The very strong exponential temperature dependence of chemical reaction rates in general makes possible the rapid combustion in the detonation mode. Two­ phase liquid droplets or dust-air mixtures are similar, but they require more physical processes (e.g. droplet break-up, phase change, mixing, etc.) prior to combustion. Thus, characteristic time or length scales associated with the combustion front are usually much larger than those of homogeneous gaseous fuel-air mixtures. The essential mechanisms of propagation of the combustion waves, however, are similar. In between the two extremes of laminar detlagration and detonation, there is an almost continuous spectrum of burning rates where turbulence plays the dominant role in the combustion process. Due to space limitations, only homogeneous gaseous fuel-air detonations are considered in this article.

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Citations
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Journal ArticleDOI

Stability of Chapman–Jouguet detonations for a stiffened-gas model of condensed-phase explosives

TL;DR: In this article, the analysis of the linear stability of a planar Chapman-Jouguet detonation wave is reformulated for an arbitrary caloric (incomplete) equation of state in an attempt to better represent the stability properties of detonations in condensed phase explosives.
Journal ArticleDOI

Wave dynamic processes in cellular detonation reflection from wedges

TL;DR: In this paper, the detonation reflection from wedges is investigated for the wave dynamic processes occurring in the wave front, including transverse shock motion and detonation cell variations behind the Mach stem.
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Sensitization of Hydrocarbon-Oxygen Mixtures to Detonation via Cool Flame Oxidation

TL;DR: In this article, the effect of cool flame partial oxidation on the detonation sensitivity of hydrocarbons was experimentally investigated by measuring the explosion cell size using the smoked-foil technique, and the results showed that the cell pattern becomes very regular at high temperature but the average cell size practically does not change.
Journal ArticleDOI

On the self-similarity of diffracting gaseous detonations and the critical channel width problem

TL;DR: In this article, a closed-form model was proposed to predict the detonation quenching for 2D channels, based on Whitham's geometric shock dynamics, coupled with a shock evolution law based on shocks sustained by a constant source.
ReportDOI

The effect of initial temperature on flame acceleration and deflagration-to-detonation transition phenomenon

TL;DR: In this article, the authors used a standard automobile diesel engine glow plug to ignite the test mixture at one end of the detonation tube and observed that the distance required for the flame to accelerate to the point of detonation initiation, referred to as the run-up distance, was a function of both the hydrogen mole fraction and the mixture initial temperature.
References
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Journal ArticleDOI

The critical tube diameter for detonation failure in hydrocarbon-air mixtures☆

TL;DR: In this paper, the critical tube diameters dc for the successful transformation of a planar to a spherical detonation have been measured in nine gaseous fuels (CH4, C2H2, C 2H4, c2H6, C3H8, C4H10, MAPP and H2) in stoichiometric fuel-oxygen mixtures diluted with nitrogen at atmospheric initial pressure.
Journal ArticleDOI

Chemical kinetics of hydrocarbon oxidation in gaseous detonations

TL;DR: In this article, a theoretical model including a detailed chemical kinetic reaction mechanism for hydrocarbon oxidation was used to examine detonation properties for mixtures of fuel, including methane, ethylene, acetylene, and methanol.
Journal ArticleDOI

On the measure of the relative detonation hazards of gaseous fuel-oxygen and air mixtures

TL;DR: In this article, the critical energy for direct initiation of spherical detonation for eight gaseous fuels (C 2 H 2, C 2 H 4 O, C 2 HO 4 O, C 3 H 6, C 1 H 8, CH 4 and H 2 ) have been measured using a planar detonation from a linear tube for initiation.
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