We study dynamics of filling of an initially empty finite medium by diffusing particles and , which arise on the surface upon dissociation of molecules, impinging on it with a fixed flux density , and desorb from it by the reaction . We show that once the bulk diffusivities differ (), there exists a critical flux density , above which the relaxation dynamics to the steady state is qualitatively changed: on time dependencies of ( being the steady state concentration at ) a maximum appears, the amplitude of which grows both with and with ratio. In the diffusion-controlled limit at the reaction “selects” the {\it universal laws} for the particles number growth and the evolution of the surface concentrations $c_{As}\propto t^{-1/4},c_{Bs}\propto t^{1/4}$, which are approached by one of the {\it two characteristic regimes} with the corresponding hierarchy of the intermediate power-law asymptotics. In the first of these goes through a comparatively {\it sharp} max, the amplitude of which is -independent, in the second one goes through a {\itplateau-like} max, the amplitude of which is -independent. We demonstrate that on the main filling stage the evolution of the ${\cal N}(t)/{\cal N}{e}, c{As}(t)/c_{e},c_{Bs}(t)/c_{e}$ trajectories with changing or between the limiting regimes is unambiguously defined by the value of the scaling parameter ( being the reduced flux density) and is described by the set of {\it scaling laws}, which we study in detail analytically and numerically.

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