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100   5  Simulating Chemical Dissolution Front Instabilities in Fluid-Saturated Porous Rocks

            planar dissolution front propagates in the full space. Since the dissolution front is a
            plane, the problem described in Eqs. (5.11), (5.12) and (5.13) degenerates into a one-
            dimensional problem. For this particular case, analytical solutions can be obtained
            for both the propagation speed of the dissolution front and the downstream pressure
            gradient of the pore-fluid. The second special case to be considered is an asymptotic
            problem, in which the solid molar density greatly exceeds the equilibrium concen-
            tration of the chemical species, implying that the region of a considerable porosity
            change propagates very slowly within the fluid-saturated porous medium. In this
            particular case, it is possible to derive a complete set of analytical solutions for the
            pore-fluid pressure, chemical species concentration and porosity within the fluid-
            saturated porous medium. In addition, it is also possible to investigate the reactive
            infiltration instability associated with the dissolution front propagation in this par-
            ticular case (Chadam et al. 1986).

            5.1.2.1 The First Special Case

            In this special case, the planar dissolution front is assumed to propagate in the pos-
            itive x direction, so that all quantities are independent of the transverse coordinates
            y and z. For this reason, Eqs. (5.11), (5.12) and (5.13) can be rewritten as follows:


                                   ∂φ   ∂       ∂p
                                      −     ψ(φ)    = 0,                 (5.15)
                                   ∂t   ∂x      ∂x
             ∂        ∂        ∂C         ∂p            A p
              (φC) −     φD(φ)    + Cψ(φ)     + ρ s k chemical  (φ f − φ)(C − C eq ) = 0,
            ∂t       ∂x        ∂x         ∂x            V p
                                                                         (5.16)
                            ∂φ          A p
                               + k chemical  (φ f − φ)(C − C eq ) = 0.   (5.17)
                            ∂t          V p

              If the chemical species is initially in an equilibrium state and fresh pore-fluid is
            injected at the location of x approaching negative infinite, then the boundary condi-
            tions of this special problem are expressed as
                                                  ∂p
              lim C = 0,     lim φ = φ f ,    lim    = p   fx  (Upstream boundary),
             x→−∞           x→−∞            x→−∞ ∂x
                                                                         (5.18)

                                                ∂p
             lim C = C eq ,  lim φ = φ 0 ,  lim    = p 0x  (Downstream boundary),

            x→∞             x→∞            x→∞ ∂x
                                                                         (5.19)

            where φ 0 is the initial porosity of the porous medium; p is the pore-fluid pressure
                                                         fx
            gradient as x approaching negative infinite in the upstream of the pore-fluid flow; p
                                                                             0x
            is the unknown pore-fluid pressure gradient as x approaching positive infinite in the

            downstream of the pore-fluid flow. Since p drives the pore-fluid flow continuously
                                              fx
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