2 E.CARIAGA, F.CONCHA, AND M.SEP´ULVEDA
any CFL conditions.Our numerical scheme consists in an combined approach, i.e, for the convectiveterm we apply a finite volume scheme, upwind Godunov, and for the diffusive termwe apply the P1 finite element method. This combined approach was applied byin [1], where their mathematical problem consists in a nonlinear, degenerate, andconvection-diffusion equation, and without reaction term. Our mathematical prob-lem considers a reactive term, a system formed by a convection-diffusion-reactionequation and an ordinary differential equation, non homogeneous Neumann bound-ary conditions, which corresponds to the physical behavior of the irrigation andinfiltration processes in heap leaching.The paper is organized as follows. In section 2, we state the compositional flowmodel for the volumetric concentration of sulfuric acid in liquid phase and for thecopper’s ions in liquid and solid phase. In section 3 we state the finite volumescheme, where a Godunov’s scheme is used for the approximation of the convectiveterm. Additionally, for the diffusive term, let us consider a standard
P
1
-FEM. Insections 4 and 5 we present the main convergence results, for sulfuric acid equa-tion and for the copper system, respectively. We derive
L
∞
,
weak BV
and
BV
estimates. Finally, in section 6 we report some computational experiments.2.
Compositional Flow Model.
We considers a two phase (liquid and gaseous phase)-two component (sulfuricacid and copper) system 2p2c, in the porous medium formed by the heap. Let aREV (
representative elementary volume
) (see [3, 10] for more details). The porosity
φ
of the porous medium is defined as the ratio between the
volume of the pore spacewithin the
REV and
the volume of
REV, and the saturation of phase
α
=
w,n
(where
α
=
w
is the liquid phase and
α
=
n
is the gaseous phase),
s
α
, is defined asthe ratio between the
volume of fluid
α
within the
REV and the
volume of the porespace within the
REV. We impose the customary property that the fluids fill thevolume:
s
w
+
s
n
= 1. A mass balance must be specified for each component. Themass balance equations for the transport of component
κ
(
κ
=
a
for the sulfuricacid, and
κ
=
c
for the copper) in
α
-phase can be written as [2], [10]:(2.1)
∂
(
θ
α
c
ακ
)
∂t
+
·
(
c
ακ
u
α
−
D
(
u
α
)
c
ακ
) + Φ
α
= 0,where
c
ακ
is the volumetric concentration defined as the ratio between the
mass of component
κ
in phase
α
and the
volume of phase
α
,
θ
α
:=
φs
α
, is the liquid content,
u
α
is the
Darcy’s flow of phase
α
, Φ
α
[
kg/m
3
·
s
] is the irreversible rate of soluteremoved (or added) from (to) the liquid solution,
D
is the dispersity-diffusion tensorgiven by
D
ij
:=
α
L
|
u
α
|
δ
ij
+ (
α
L
−
α
T
)
u
i
u
j
|
u
α
|
+
D
m
δ
ij
, where
α
L
and
α
T
are thelongitudinal and transverse dispersities, respectively,
δ
ij
= 1 if
i
=
j
and
δ
ij
= 0 if
i
=
j
, and
D
m
is the molecular diffusion coefficient (in this paper we set
D
m
= 0).By another hand, if is assumed that there is a isotherm between the liquid phase andthe solid phase
ϕ
ακ
=
ϕ
ακ
(
c
ακ
), defined as the ratio between the
mass of component in solid phase
and
mass of solid phase
, then (using the assumption that sorptiononly occurs from the liquid to the solid phase), the equation for the liquid phasecan be modified to include adsorption:(2.2)
∂
(
φ
s
ρ
s
ϕ
ακ
)
∂t
+
∂
(
θ
α
c
ακ
)
∂t
+
·
(
c
ακ
u
α
−
D
(
u
α
)
c
wκ
) + Φ
α
= 0,
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