10.1201 9781003308539-4 Chapterpdf
10.1201 9781003308539-4 Chapterpdf
10.1201 9781003308539-4 Chapterpdf
49
50 Poro-Elastic Theory with Applications to Transport in Porous Media
∂F ∂ f ∂ξ ∂F ∂ f ∂ξ ∂ f ∂f ∂f
= , = + = vs + , (3.1)
∂z ∂ ξ ∂ z ∂t ∂ ξ ∂t ∂t ∂ξ ∂t
where ρs is the soil grain density, n = e/(1 + e) is the current porosity, and n0 =
n(z, 0) is the initial porosity. Note that, for constant ρs , the Jacobian, M, for the
coordinate transformation is
∂ξ 1 − n0 1+e
M= = = , (3.3)
∂z 1−n 1 + e0
where e0 is the initial void ratio.
The continuity equation for the fluid phase (i.e., pore-water) is
∂ ∂ξ ∂
nSr ρ f = − (ρ f q), (3.4)
∂t ∂z ∂z
∂ξ ∂ p ∂ 1 ∂ ∂ p ∂z
∂ξ
nSr β + Sr = kv , (3.6)
∂ z ∂t ∂t ∂z ρf g ∂z ∂z ∂ξ
where the compressibility of pore fluid (β ) is defined in (2.2).
Because n and n0 (implicitly embedded in ∂ ξ /∂ z) appear simultaneously, and n
is unknown, (3.6) can not be directly solved in terms of p. In the following derivation,
it turns out that once the relationship between the derivative of p (with respect to t
and a) and the corresponding derivative of e is known, it is straightforward to convert
(3.6) to an equation in terms of e.
Assuming self-weight is negligible due to the relatively small thickness of the
CCL (Zhang et al., 2012a), the vertical force equilibrium is
∂σ
= 0, (3.7)
∂z
where σ (now a function of t only) is the total normal stress of the soil and the z
coordinate is vertically upwards. Assuming the compressive normal stress is positive,
i.e., σ = σ 0 + p (σ 0 is the effective normal stress), (3.7) leads to:
∂p ∂ ∂z 1 + e0 1 ∂ e
= −σ 0 + σ = , (3.8)
∂ξ ∂z ∂ξ 1 + e αv ∂ z
where αv = −de/dσ 0 is the coefficient of soil compressibility.
In the absence of self-weight, the rate of change of total stress at an arbitrary
location equals that of the external top loading,
∂σ ∂Q
= , (3.9)
∂t ∂t
where Q is the external load. The rate of change of the excess pore water pressure in
the time domain is
∂p ∂ ∂Q 1 ∂e
= (σ − σ 0 ) = + . (3.10)
∂t ∂t ∂t αv ∂t
Substituting (3.3), (3.8), (3.10) into (3.6) yields:
eSr β Sr ∂ e 1 + e0 ∂ kv ∂e Sr β e ∂ Q
+ − =− . (3.11)
(1 + e0 )αv 1 + e0 ∂t ρ f g ∂ z αv (1 + e) ∂ z 1 + e0 ∂t
52 Poro-Elastic Theory with Applications to Transport in Porous Media
For the fully saturated case and when the CPW is neglected, i.e., β = 0, (3.11)
reduces to:
1 ∂ e 1 + e0 ∂ kv ∂e
= , (3.12)
1 + e0 ∂t ρ f g ∂ z αv (1 + e) ∂ z
where S is the mass of solute sorbed on or within the solid phase per unit mass of
the solid phase and fa→s
0 denotes rate of solute loss in the water phase by solid phase
sorption.
The mass conservation equation for solute in the fluid phase is
∂ Jf
∂ ∂ξ 0
nSr c f =− − fa→s , (3.14)
∂t ∂z ∂z
where c f is the concentration of the solute in the pore fluid. In (3.14), the term ∂ ξ /∂ z
comes from the volumetric change (Peters and Smith, 2002) and J f represents solute
flux in the fluid phase, which is described by (Peters and Smith, 2002):
nSr D ∂ c f
J f (z,t) = nSr (v f − vs )c f − , (3.15)
M ∂z
where D is the hydrodynamic dispersion coefficient. It is given by the sum of the
effective diffusion coefficient (De ) and the coefficient of mechanical dispersion (Dm ):
Dm = αL v f − vs , (3.16)
∂ nSr D ∂ c f
∂ ∂ξ ∂
nSr c f + (1 − n)ρs S nSr (v f − vs )c f . (3.17)
= −
∂t ∂z ∂z M ∂z ∂z
1D finite strain coupled model for consolidation and solute transport 53
The above equation can be further simplified with Darcy’s Law, (3.5), and the
mass balance equations for both solid and fluid phases, (3.2) and (3.4), respectively.
(3.17) can then be expressed as:
∂ξ ∂cf ∂ ξ ∂ S ∂ nSr D ∂ c f kv ∂ p ∂ c f
nSr + (1 − n)ρs = +
∂ z ∂t ∂ z ∂t ∂ z M ∂z ρf g ∂ξ ∂z
(3.18)
∂ ξ ∂ p β kv ∂ p ∂ p
+ nSr β − cf .
∂ z ∂t ρ f g ∂ ξ ∂ z
e ρs Kd ∂ c f ∂ e(1 + e0 ) ∂ c f
Sr + = Sr D
1 + e0 1 + e0 ∂t ∂ z (1 + e)2 ∂ z
kv 1 + e0 ∂ e ∂ c f
+
ρ f g αv (1 + e) ∂ z ∂ z
e
∂Q 1 ∂e
(3.19)
+ β Sr +
1 + e0 ∂t αv ∂t
2 #
kv 1 + e0 ∂ e
− cf ,
ρ f gαv2 1 + e ∂ z
which is identical to Eq. (4) of Lewis et al. (2009) and Eq. (44) in Peters and Smith
(2002).
∂p ∂ 2u 1 ∂ ∂p
Sr n0 β + Sr = kv , (3.21a)
∂t ∂t∂ ξ ρw g ∂ ξ ∂ξ
54 Poro-Elastic Theory with Applications to Transport in Porous Media
2(1 − ν) ∂ 2 u ∂p
G = , (3.21b)
(1 − 2ν) ∂ ξ 2 ∂ξ
and
∂cf ∂ 2c f kv ∂ p ∂ 2 c f
[Sr n0 + (1 − n0 ) ρs Kd ] = Sr n0 De 2
− αL
∂t ∂ξ ρw g ∂ ξ ∂ ξ 2
∂cf ∂p ∂ 2u
+ −αL Sr n0 β − αL Sr
∂ξ ∂t ∂ ξ ∂t
2
αL β kv ∂ p ∂ 2u
+ + Sr De (1 − n0 ) 2
ρw g ∂ξ ∂ξ
(3.21c)
kv ∂ p ∂u
+ − [Sr n0 + (1 − n0 ) ρs Kd ]
ρw g ∂ ξ ∂t
2
∂p kv ∂p
+ Sr n0 β cf −β cf
∂t ρw g ∂ ξ
∂u ∂ p
+ Sr n0 β cf ,
∂t ∂ ξ
where u is the soil displacement, G is the shear modulus and ν is Poisson’s ratio.
The constant material coefficients can be described as:
cv ρ f g(1 − 2ν) (1 + e p )(1 − 2ν)
G= = ,
2kv (1 − ν) 2(1 − ν)αvp (3.22)
kv = k p , De = De0 ,
∂cf ρs Kd −1 ∂ 2 c f
= D 1+ . (3.23)
∂t Sr e0 ∂ξ2
The power law relationship equation for hydraulic conductivity versus water
content θ (= Sr n) is (Li and Liu, 2006):
α
θ
kv = ks , (3.28)
θs
where θs is saturated water content, and α falls in the range of 2.68 to 2.78 for clay
loam.
3.3.4 SORPTION
It has been reported that the effect of the degree of saturation on the adsorption
coefficient is insignificant from full saturation to a degree of saturation of 10%
1D finite strain coupled model for consolidation and solute transport 57
S = Kd c f . (3.31)
This assumption of a linear sorption is valid at the relatively low concentrations that
are usually found in the municipal waste disposal sites (Mathur and Jayawardena,
2008).
∂e
= 0 at z = 0. (3.32)
∂z
At the bottom drainage boundary (z = L), the excess pore pressure is zero and a
Dirichlet-type boundary condition for void ratio (e) can be derived from the effective
stress–void ratio equilibrium relationship, (3.24):
!
σL0
e = e p −Cc log , (3.33)
σ p0
Table 3.1
Values of input parameters.
Parameter Value
Maximum applied stress (ramp loading for 2 years), σa 450 kPa
Preconsolidation stress, σ p0 50 kPa
Compression index, Cc 0.2, 0.8
Preconsolidation hydraulic conductivity, k p 10−9 , 2×10−10 m/s
Constant, α 2.7
Hydraulic conductivity index, Ck 0.585
Thickness of geomembrane, h 0.0015 m
Thickness of CCL, L 1.22 m
Mass transfer coefficient of geomembrane, PG 4 × 10−11 m2 /s
Initial effective diffusion coefficient, De0 2 ×10−10 m2 /s
Free diffusion coefficient in the pore fluid, D f 10−9 m2 /s
Threshold moisture content, θt 0.05
Partitioning coefficient, Kd 0, 0.2, 1 ml/g
Dispersion, αL 0, 0.1 m
Initial void ratio, e0 ( = e p ) 1.17
Acceleration due to gravity, g 9.81 m/s2
Initial density of pore-water, ρ f 103 kg/m3
Density of the solid phase, ρs 2.7 × 103 kg/m3
Degree of saturation of clay, Sr 1, 0.9, 0.8
loading in the model of Lewis et al. (2009). The void ratio rapidly approaches a
steady value, which consequently leads to a spurious higher fluid velocity and faster
solute transport. To distinguish the cases, we label the present boundary condition at
the CCL bottom as ‘BCC’ and ‘BCL’, i.e., the boundary conditions used by Lewis
et al. (2009).
∂cf (1 + e(0,t))2 PG
c f (0,t) −C f 0 , (3.34)
(0,t) =
∂z e0 (1 + e0 ) hDe
Smith, 2002); h and PG are, respectively, the thickness and the permeation coefficient
for the solute in the geo-membrane.
The lower boundary condition for the solute concentration (c f ) is (Peters and
Smith, 2001):
∂cf
= 0, at z = L, (3.35)
∂z
which assumes negligible diffusion below the CCL base (Barry and Sposito, 1988).
−1
10
Relative concentration at CCL base, Cf/Cf0
−2
10
−3
10 LD, Constant De
LD, Decreasing De
ND
SD
Lewis et al. (2009)
−4
10
5 10 15 20 25 30 35 40
Time, t (y)
Figure 3.1 Comparison of (a) void ratio evolution and (b) breakthrough curves between the
present model (solid line) and Lewis et al. (2009) (circle). Notations: FD: finite deformation
model, SD: small deformation model, ND: no deformation model.
Cc = 0.8 and k p = 10−9 m/s. A comparison of Figure 3.2(a) (BCC) and 3.1(a) (BCL)
shows that taking σa as the maximum loading leads to a greater void ratio gradient
and a faster consolidation process, although the final value of e is very close. This
initially speeds up the solute transit slightly, and then slows it down in the long-term
(Figure 3.2(b)). The reason the trend reverses after the consolidation completes for
the ‘BCL’ case is that the higher solute concentration level during the consolidation
phase of ‘BCC’ occurs later resulting in an increased advective flux. The separation is
more obvious for the relatively soft and higher permeablility cases. In the following
sections all numerical results are based on the boundary condition ‘BCC’.
0
10
−2
10
Case 1(BCC)
−3
10 Case 2(BCC)
Case 3(BCC)
Case 1(BCL)
Case 2(BCL)
Case 3(BCL)
−4
10
0 5 10 15 20 25 30 35 40
Time, t (y)
(a) Void ratio evolution (BCC only) (b) Breakthrough curves (BCC and BCL)
Figure 3.2 Influence of Boundary condition of void ratio (e) at CCL base (a) void ratio
evolution (BCC only) and (b) breakthrough curves (Sr = 1, β = 0, αL = 0, constant De ). In
(b), solid line for ‘BCC’, and dash-dot line for ‘BCL’. Case 1: k p = 2 × 10−10 m/s, Cc =0.8;
Case 2: k p = 10−9 m/s, Cc =0.8; and Case 3: k p = 10−9 m/s, Cc =0.2.
with boundary conditions x(0,t) = Smt and x(L,t) = L was constructed to find x,
where the settlement Smt is given by:
Z L
e0 − e(ζ )
Smt = dζ . (3.38)
0 1 + e0
−0.1 −0.1
Settlement at CCL top, S (m)
−0.2 −0.2
−0.3 −0.3
−0.4 −0.4
−0.5 −0.5
kp = 2×10−10 m/s, Cc=0.8 kp = 2×10−10 m/s, Cc=0.8
kp = 10−9 m/s, Cc=0.2 kp = 10−9 m/s, Cc=0.2
0 5 10 15 20 25 30 35 40 0 20 40 60 80 100 120
Time, t (y) Time, t (y)
Figure 3.3 Consolidation settlements in a (a) saturated soil (Sr = 1) and (b) partially
saturated soils (Sr = 0.8).
Figures 3.3(a) and 3.4(a) illustrate the consolidation processes and solute
transport in a saturated soil for two cases with different compression indices (Cc )
and hydraulic conductivities (kv ). Consolidation lasts 2.2 and 34.5 y for Cc = 0.2 and
Cc = 0.8, respectively. For the ‘soft’ case, a noticeable concentration difference from
the no deformation model appears at the CCL base during consolidation, as shown in
Figure 3.4(a). The difference decreases with higher levels of sorption (Figure 3.4(a)).
The effect of consolidation on transport exists during both the consolidation and
post-consolidation stages, which is consistent with Fox (2007b). Since the advection
results in a notable concentration level at the CCL base, simplifying assumptions
such as instant deformation, pure diffusion and finite deformation without advection
modeling are not appropriate. The magnitude of solute concentration C f in Figure
3.4(a) is an order greater than that in Figure 3.4(a) . Here, the influence of sorption
is noticeable as it drastically retards the solute transport.
Figures 3.3(b) and 3.4(b) present the results for a nearly saturated soil. We see
again that soft clay consolidation has a noticeable effect on solute transport (Figure
62 Poro-Elastic Theory with Applications to Transport in Porous Media
−1
0.5 10
0.4
−2
10
0.3 k = 1 ml/g
d
0.2 −3
10
0.1
−4
10
0 0 20 40 60 80 100 120
0 5 10 15 20 25 30 35 40
Time, t (y) Time, t (y)
Kd = 0 Kd 6= 0
(a) saturated soil (Sr =1)
Relative concentration at CCL base, Cf/Cf0
k = 0.2 ml/g
d
−2
10
Relative concentration at CCL base, Cf/Cf0
0.5
0.4 −4
10
0.3
−6
kd = 1 ml/g
10
0.2
−8
10
0.1
−10
10
0 0 20 40 60 80 100 120
0 20 40 60 80 100 120
Time, t (y) Time, t (y)
Kd = 0 Kd 6= 0
(b) partially saturated soils (Sr = 0.8)
3.3(b)). However, since the effective diffusion (De ) reduces with deformation,
concentrations for the pure diffusion model surpass those of coupled models, as is
obvious for the case of Kd = 1 ml/g.
Consolidation effects are composed of the variation of void ratio and the
occurrence of pore-water flow, which in turn causes the advective transport flux.
As mentioned previously, Lewis et al. (2009) claimed the advection component can
be ignored as long as the variation of void ratio is considered. Here, we included
in Figure 3.5 the case of finite deformation without advection, i.e., advection is
removed from (3.19). Exclusion of advection underestimates the concentration level
and consequently leads to a longer transit time. In the absence of sorption, at the
nominal 10% breakthrough, a nearly twofold change occurs in the transit time; this
change increases when sorption is included.
1D finite strain coupled model for consolidation and solute transport 63
Kd = 1 ml/g
−4
10
−6
10
0 20 40 60 80 100
Time, t (y)
Figure 3.5 Effect of advection flux on concentration level at CCL base for partially saturated
cases (Sr = 0.8, with CPW, αL = 0.1 m, varying De as in (3.30)). For finite deformation model,
solid line: Cc = 0.8, k p = 2 × 10−10 m/s; dash-dot line: without advection flux in transport,
(3.19); dashed line: No deformation model.
0
10
Relative concentration at CCL base, Cf/Cf0
−1
10
−2
10
Kd = 0, Sr = 0.8
Kd = 0, Sr = 0.9
−3 Kd = 0, Sr = 1.0
10 Kd = 1 ml/g, Sr = 0.8
Kd = 1 ml/g, Sr = 0.9
Kd = 1 ml/g, Sr = 1.0
−4
10
0 20 40 60 80 100 120
Time, τ (y)
Figure 3.6 demonstrates that the higher saturation of the no-deformation (ND)
model results in faster solute transport due to the saturation (Sr )-dependent effective
diffusion; the gap is larger in the presence of sorption. Concentrations predicted
by the coupled finite deformation and solute transport model are shown in Figure
3.7. For cases with parameters Cc = 0.8 and k p = 10−9 m/s, consolidation lasts for
approximately 12.8 y. Higher saturation results in faster solute transport because of
64 Poro-Elastic Theory with Applications to Transport in Porous Media
greater effective diffusion, regardless of the sorption. For decreasing De , the transit
time increases, as shown in Figure 3.7(a). With sorption, finite deformation with
Sr = 0.8 and constant De leads to almost the same concentration as for the ND
model (Figure 3.7(b)). Again, this demonstrates that the effect of unsaturation is
more apparent in the presence of sorption. Interestingly, with both sorption and
decreasing De taken into account, finite deformation (FD) models will not always
produce faster solute transport (Figure 3.7(a)). During consolidation and in the early
post-consolidation stage, the FD models have a faster transit, but then are surpassed
by the ND model because the effective diffusion is reduced due to compaction.
However, the decreasing De with compaction is inevitable. In the field, VOC has
been shown to appear earlier than predicted by the pure diffusion model has been
observed (Peters and Smith, 2002). Possible explanations are: (1) the constitutive
relationships for soil parameters are not accurate enough; or (2) other factors, such
as heat transfer, should be also included in the model. Relative concentration at CCL base, Cf/Cf0
Relative concentration at CCL base, Cf/Cf0
0.4
FD, Sr = 1.0
1e−2
FD, S = 0.9
r
0.3 FD, Sr = 0.8
ND, Sr= 1.0 1e−4
0.2
1e−6
FD, Sr = 1.0
0.1 FD, Sr = 0.9
1e−8
FD, Sr = 0.8
ND, Sr= 1.0
0 0
0 10 20 30 40 0 20 40 60 80 100 120
Time, τ (y) Time, τ (y)
Kd = 0 Kd = 1 ml/g
(a) The case with decreasing De
Relative concentration at CCL base, Cf/Cf0
0.4 0.15
0.3
0.1
0.2
0.05
0.1
0 0
0 10 20 30 40 0 20 40 60 80 100 120
Time, τ (y) Time, τ (y)
Kd = 0 Kd = 1 ml/g
(b) The case with a constant De
Figure 3.7 Concentration level at CCL base for partially saturated cases with decreasing De .
(Cc = 0.8, k p = 10−9 m/s). Notation: FD: finite deformation model and ND: no deformation
model.
1D finite strain coupled model for consolidation and solute transport 65
−6
10
−8
10
−10
10
1.5 2 2.5 3
Time, τ (y)
Figure 3.8 Effect of CPW on concentration level at CCL base for partially saturated cases
(Sr = 0.8) with varying De and without sorption (Kd = 0). Solid lines: Cc = 0.8, k p = 2×10−10
m/s; Dashdot lines: Cc = 0.8, k p = 10−9 m/s; Dotted lines: Cc = 0.2, k p = 10−9 m/s. Cross
symbol: with CPW; circle symbol: without CPW (β = 0).
To investigate further the influence of CPW, three models examining the three
terms containing β are considered here.
eSr β ∂ e
• Model A: eliminate (1+e0 )αv ∂t from (3.11);
Sr β e ∂ Q
• Model B: eliminate − 1+e 0 ∂t
from (3.11);
• Model C: eliminate the term involving β from (3.19).
As shown in Figure 3.9, each of the missing terms leads to a large deviation from
the full model, so all terms involving β should be retained for the cases considered.
66 Poro-Elastic Theory with Applications to Transport in Porous Media
0
10
−2
10
−3
10
Complete model
Model A
Model B
Model C
−4
10
0 10 20 30 40
Time, τ (y)
Figure 3.9 Significance of each term involving β on concentration level at CCL base for
partially saturated cases (Sr = 0.8, Cc = 0.8, k p = 2 × 10−10 m/s) with varying De and without
sorption (Kd = 0).
−1
10
−2
10
−3
10
−4
10
0 5 10 15 20 25 30 35 40
Time, τ (y)
Figure 3.10 Effect of dispersion on concentration level at CCL base for partially saturated
cases (Sr = 0.8) with varying De and without sorption (Kd = 0). Solid lines: Cc = 0.8, k p =
2 × 10−10 m/s; Dashdot lines: Cc = 0.8, k p = 10−9 m/s; Dotted lines: Cc = 0.2, k p = 10−9
m/s. Cross symbol: αL = 0.1 m; circle symbol: αL = 0 (no dispersion).
0
Relative concentration at CCL base, Cf/Cf0
10
−20
10
−1
10
−22
−2 10
10
FD −24
−3
10 FD, CD 10
FD, NLGD
FD, NCPW
−4
ND −26
10 10
0 10 20 30 40 0 0.5 1 1.5 2
Time, τ (y) Time, τ (y)
Figure 3.11 Comparison of the concentration level at CCL base for various variable
associative in partially saturation soils (Sr = 0.8, Cc = 0.8, k p = 10−9 m/s). Notation: FD: finite
deformation model; CD: constant De ; NLGD: excluding the dispersion; NCPW: excluding the
CPW; ND: no deformation model.
3.6 SUMMARY
In this chapter, a finite deformation model for coupling consolidation and solute
transport processes in partially saturated soil has been presented. It was applied
to predict the VOC breakthrough in a landfill clay liner. CPW, dispersion, the
nonlinear variation of soil compaction, hydraulic conductivity and effective diffusion
are included in the model. Based on the numerical simulation results, the following
conclusions can be drawn.