Pseudo-steady states in the model of the Bray–Liebhafsky oscillatory reaction

Abstract

The main pseudo-steady states in the process of catalytic hydrogen peroxide decomposition are analysed. The dominant steady states during the monotonic and oscillatory evolution, well known experimentally, are defined by stoichiometric network analysis of the model for this process. The trajectories for the evolution of the system in the phase space in the vicinity of the unstable pseudo-steady state where oscillatory behaviour is obtained, are also calculated. The adjustment of the phase trajectory to the corresponding oscillation is proposed as an additional criterion for the selection of the kinetic parameters necessary for numerical simulation. The calculation procedure is general, independent of the model under consideration.

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