A Lagrangian framework is used for analysing reactive solute transport by a steady random velocity field, which is associated with flow through a heterogeneous porous formation. The reaction considered is kinetically controlled sorption–desorption. Transport is quantified by the expected values of spatial and temporal moments that are derived as functions of the non-reactive moments and a distribution function which characterizes sorption kinetics. Thus the results of this study generalize the previously obtained results for transport of non-reactive solutes in heterogeneous formations (Dagan 1984; Dagan et al. 1992). The results are illustrated for first-order linear sorption reactions. The general effect of sorption is to retard the solute movement. For short time, the transport process coincides with a non-reactive case, whereas for large time sorption is in equilibrium and solute is simply retarded by a factor R = 1+ K d , where K d is the partitioning coefficient. Within these limits, the interaction between the heterogeniety and kinetics yields characteristic nonlinearities in the first three spatial moments. Asymmetry in the spatial solute distribution is a typical kinetic effect. Critical parameters that control sorptive transport asymptotically are the ratio ε r between a typical reaction length and the longitudinal effective (non-reactive) dispersivity, and K d . The asymptotic effective dispersivity for equilibrium conditions is derived as a function of parameters ε r and K d . A qualitative agreement with field data is illustrated for the zero- and first-order spatial moments.
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Cvetković et al. (1994) studied this question.
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