Dynamics of the reaction-diffusion system A + B 0 with input of particles
Abstract
We study dynamics of filling of an initially empty finite medium by diffusing particles A and B, which arise on the surface upon dissociation of AB molecules, impinging on it with a fixed flux density I, and desorb from it by the reaction A + B AB 0. We show that once the bulk diffusivities differ (p=DA/DB<1), there exists a critical flux density Ic(p), above which the relaxation dynamics to the steady state is qualitatively changed: on time dependencies of cAs/ce (ce being the steady state concentration at t ∞) a maximum appears, the amplitude of which grows both with I and with DB/DA ratio. In the diffusion-controlled limit I Ic at p 1 the reaction "selects" the universal laws for the particles number growth NA= NB t1/4 and the evolution of the surface concentrations cAs t-1/4,cBs t1/4, which are approached by one of the two characteristic regimes with the corresponding hierarchy of the intermediate power-law asymptotics. In the first of these cAs goes through a comparatively sharp max(cAs/ce) I1/6, the amplitude of which is p-independent, in the second one cAs goes through a -like max(cAs/ce) p-1/4, the amplitude of which is I-independent. We demonstrate that on the main filling stage the evolution of the N(t)/ Ne, cAs(t)/ce, and cBs(t)/ce trajectories with changing p or J between the limiting regimes is unambiguously defined by the value of the scaling parameter K=p3/2J (J being the reduced flux density) and is described by the set of scaling laws, which we study in detail analytically and numerically.
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