Planar detonation structure for chain-branching kinetics with large activation energy and small initiation rate

2007 ◽  
Vol 20 (4-6) ◽  
pp. 570-577 ◽  
Author(s):  
Z. Liang ◽  
L. Bédard-Tremblay ◽  
L. Bauwens
2009 ◽  
Vol 32 (2) ◽  
pp. 2339-2347 ◽  
Author(s):  
Laurie Bédard-Tremblay ◽  
Josue Melguizo-Gavilanes ◽  
Luc Bauwens

1955 ◽  
Vol 5 (1) ◽  
pp. 637-641 ◽  
Author(s):  
J. Van Wonterghem ◽  
A. Van Tiggelen

The effect of the magnitude of activation energy on reaction rates has been examined. The conclusions suggest that a valid approximation to combustion mechanisms should be obtainable from a consideration of a single rate-controlling chain-branching and a single rate-controlling chain-breaking step. This concept has been applied in turn to homogeneous auto-ignition, ignition lags, limits of inflammability, flame propagation and burning velocities, resulting in a simple co-ordinating scheme. The formulae derived imply methods of identification of the rate-controlling processes from measurable flame properties.


1997 ◽  
Vol 339 ◽  
pp. 89-119 ◽  
Author(s):  
MARK SHORT ◽  
JAMES J. QUIRK

The nonlinear stability of a pulsating detonation wave driven by a three-step chain-branching reaction is studied. The reaction model consists sequentially of a chain-initiation step and a chain-branching step, both governed by Arrhenius kinetics, followed by a temperature-independent chain-termination step. The model mimics the essential dynamics of a real chain-branching chemical system, but is sufficiently idealized that a theoretical analysis of the instability is possible. We introduce as a bifurcation parameter the chain-branching cross-over temperature (TB), which is the temperature at which the chain-branching and chain-termination rates are equal. In the steady detonation structure, this parameter controls the ratio of the chain-branching induction length to the length of the recombination zone. When TB is at the lower end of the range studied, the steady detonation structure, which is dominated by the temperature-independent recombination zone, is found to be stable. Increasing TB increases the length of the chain-branching induction region relative to the length of the recombination zone, and a critical value of TB is reached where the detonation becomes unstable, with the detonation shock pressure evolving as a single-mode low-frequency pulsating oscillation. This single-mode nonlinear oscillation becomes progressively less stable as TB is increased further, persisting as the long-term dynamical behaviour for a significant range of TB before eventually undergoing a period-doubling bifurcation to a two-mode oscillation. Further increases in TB lead to a chaotic behaviour, where the detonation shock pressure history consists of a sequence of substantive discontinuous jumps, followed by lower-amplitude continuous oscillations. Finally, for further increases in TB a detonability limit is reached, where during the early onset of the detonation instability, the detonation shock temperature drops below the chain-branching cross-over temperature causing the wave to quench.


Shock Waves ◽  
2006 ◽  
Vol 15 (3-4) ◽  
pp. 247-257 ◽  
Author(s):  
Z. Liang ◽  
L. Bauwens

2012 ◽  
Vol 550-553 ◽  
pp. 736-741
Author(s):  
Peng Peng Li ◽  
Shi Yuan Yang ◽  
Shan Xue

Dynamic rheological results of 17 commercial and noncommercial metallocene-catalyzed polyethylenes, such as shear thinning index(SHI), modulus of crossover point of store modulus and loss modulus (Gco) and flow activation energy(Ea), are presented. The effects of molecular weight distribution(MWD), and degree of short chain branching (SCB) determined by gel permeation chromatography (GPC) and FTIR, were analyzed. Plots of SHI versus MWD revealed the influence of branching level on the shear thinning behavior of polyethylenes. Gcowas observed scaling with MWD for metallocene-catalyzed polyethylenes and the correlation between them was generated by MWD=193378*Gco. Correlation between flow activation energy measured by dynamic temperature sweep at low frequency and short chain branch-0.9038was also established for metallocene polyethylenes as SCB=7*10-8*Ea6.024. Thus, an alternative single rheological method, based on the effect of molecular structural parameters on dynamic rheological behaviors, was proposed to evaluate the polydispersity and short chain branching of metallocene-catalyzed polyethylene.


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