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Quasi-Steady-State and Partial-Equilibrium Approximations in Chemical Kinetics: One Stage Beyond the Elimination of a Fast Variable

revised on 15.04.2021, 09:05 and posted on 16.04.2021, 04:56 by Agnès Pellissier-Tanon, Gabriel Morgado, Ludovic Jullien, Annie Lemarchand
Classical approximations in chemical kinetics, the quasi-steady-state approximation (QSSA) and the partial-equilibrium approximation (PEA), are used to reduce rate equations for the concentrations and the extents of the reaction steps, respectively. We make precise two conditions on the rate constants necessary and sufficient to eliminate a well-chosen variable in the vicinity of a steady state. The first condition expresses that dynamics admits a small characteristic time associated with a fast variable. The second condition ensures that the fast variable is a concentration for QSSA and an extent for PEA. Both approximations exploit the zeroth order of a singular perturbation method. Eliminating a fast variable does not mean that it has reached a steady state. The fast evolution is considered over and the slow evolution of the eliminated variable is governed by the slow variables. The evolution of the slow variables occurs on a slow manifold in the space of the concentrations or the extents. In some cases the dynamics of the slow variables can be associated with a reduced chemical scheme. QSSA and PEA are applied to three chemical schemes associated with linear and nonlinear dynamics. We find that QSSA cannot be identified with the elimination of a reactive intermediate. The nonlinearities of the rate equations induce a more complex behavior.


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Sorbonne Universite



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Version Notes

version 2. Modofication of Eq. (17)