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Reactive Transport in Porous Media
Daniel M. Tartakovsky
Department of Mechanical & Aerospace Engineering
University of California, San Diego
Alberto Guadagnini, Politecnico di Milano, Italy
Peter C. Lichtner, Los Alamos National Laboratory
Outline
1. Mathematics of Chemical Reactions
2. Uncertainty Quantification & Stochastic PDEs
3. PDF Methods
4. Upscaled effective reaction rate
5. Conclusions
Mathematics of Chemical Reactions
• Any general reversible chemical reaction with n reacting species
A1, A2, ...An can be represented as
α1A1 + α2A2 + ... + αmAmαm+1Am+1 + ... + αnAn
• The concentration of species Ai is denoted by
Ci ≡ [Ai], i = 1, . . . , n; C =mass of species
volume of solution=
[M ][L3]
• Each reaction process satisfies a (nonlinear) rate equation
dCi
dt= R(C1, C2, ...Cn), i = 1, . . . , n
Reactive Transport
• Transport equations: Mass conservation
Advection
Molecular diffusion
Kinematic dispersion
Chemical reaction
ω∂Ci
∂t= ∇ · (D∇Ci)−∇ · (uCi) + R(C1, . . . , Cn), i = 1, . . . , n
Example 1: Adsortption
• The mass concentration of the adsorbed substance:
C2 =mass of adsorbed solute
unit mass of solid
• The mass of solids in a unit volume of a porous medium:
(1− ω)ρs =unit mass of solids
unit volume of porous media
• The mass of a substance bound to solids in a unit volume:
(1− ω)ρsC2
Example 1: Adsorption (cndt.)
• The change in mass per unit volume per unit time:
R = −(1− ω)ρs∂C2
∂t, (R ≤ 0)
• If adsorption is instantaneous,
C2 ≈ KdC1, Kd ≡ the distribution coefficient
• Transport equation (retardation coefficient),
ωR∂C1
∂t= ∇ · (D∇C1)−∇ · (uC1) , Rc = 1 +
1− ω
ωρsKd
Example 2: Dissolution
• Dissolution
αA A(s), C ≡ [A]
• Reaction rate equation (effective reaction rate)
R ≡ dC
dt= −αk(Cα − Cα
eq)
• Transport equation
ω∂C
∂t= ∇ · (D∇C)−∇ · (uC)− αk(Cα − Cα
eq)
Reaction coefficients
• Relation to the structure of a porous medium
Kd, Rc, k = F1(surface areas) = F2(pore structure)
• Effective reaction rate
k ≈ k0a, a ∼ (1− ω)λl
k0 — laboratory measured rate constant
a — specific surface area
λ — roughness factor
l — characteristic grain size
Outline
1. Mathematics of Chemical Reactions
2. Uncertainty Quantification & Stochastic PDEs
3. PDF Methods
4. Upscaled effective reaction rate
5. Conclusions
Uncertainty in Environmental Modeling
• Wisdom begins with the acknowledgment of uncertainty—of the
limits of what we know. David Hume (1748), An Inquiry Concerning
Human Understanding
• Most physical systems are fundamentally stochastic (Wiener, 1938;
Frish, 1968; Papanicolaou, 1973; Van Kampen, 1976):
• Model & Parameter uncertainty
– Heterogeneity– Lack of sufficient data– Measurement noise∗ Experimental errors∗ Interpretive errors
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• Randomness as a measure of ignorance
Alternative Frameworks for UQ
• Ignore parameter uncertainty
• Fuzzy logic
• Interval mathematics
• Probabilistic/stochastic approaches
– Geostatistics
– Monte Carlo simulations
– Moment equations
– PDF methods
– Etc.
• Upscaling (homogenization)
Stochastic Framework
• Reaction rate k(x)
• Random field k(x, ω)
• Ergodicity
• Transport equations become
stochastic
• Solutions are given in terms of
PDFs
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Probabilistic Description of k
Relationship between the distributions of the grain size l and effective
rate constant k: pk(k)dk ≡ pl(l)dl
• Cubic grains
pk(k) =6λφsk0
k2pl
(6λφsk0
k
)
• Spherical grains
pl(l) ≡1
lσ2l
√2π
e−(ln l−µl)2/(2σ2
l )0 1 2 3
Normalized k
0
0.5
1
1.5
2
Nor
mal
ized
dis
trib
utio
n (p
df)
of k
Stochastic Upscaling
• Meso-scale transport equation:
∂c
∂t= −∇ · (vc) + fk(c), fk = −αk(cα − Cα
eq)
• Uncertain (random) parameters: velocity v & reaction rates k
• Effective transport equation:
∂c
∂t= −∇ · (veffc)− αkeff(cα − Cα
eq)
• Reynolds decomposition
k = k + k′, k ≡∫
kpk(k)dk, k′ = 0
• Stochastic upscaling vs. deterministic upscaling
Traditional Approaches
• Effective transport equation:
∂c
∂t= −∇ · (veffc)− αkeff(cα − Cα
eq)
• Note that
keff 6= k ⇒ keff = keff(k, σ2k, lk, . . .)
• Standard approaches:
– keff ≈ k
– Linearization fκ(c) = fκ(c) + . . .
Outline
1. Mathematics of Chemical Reactions
2. Uncertainty Quantification & Stochastic PDEs
3. PDF Methods
4. Upscaled effective reaction rate
5. Conclusions
PDF Approach
• Motivation
– To avoid the linearization
– To obtain complete statistics
• Raw distribution:
Π(c, C;x, t) ≡ δ(c(x, t)− C)
• Probability density function (PDF):
pc(C;x, t) = 〈Π(c, C;x, t)〉
• Concentration moments:
〈cn(x, t)〉 =∫
Cnpc(C;x, t)dC
PDF Equation & Closures
• Stochastic PDE for the raw distribution inR4: x = (x1, x2, x3, C)T
∂Π∂t
= −∇ · (vΠ) v = (v1, v2, v3, fκ)T
• Deterministic PDE for PDF
∂p
∂t= −∇ · (〈v〉p)− ∇ · 〈v′Π′〉
• Closure approximations
– Direct interaction approximation (Kraichnan, 1987)
– Large-eddy simulations (Koch and Brady, 1987)
– Weak approximation (Neuman, 1993)
– Closure by perturbation (Cushman, 1997)
Outline
1. Mathematics of Chemical Reactions
2. Uncertainty Quantification & Stochastic PDEs
3. PDF Methods
4. Upscaled effective reaction rate
5. Conclusions
Example: One-Dimensional Batch System
• Mesoscale transport equation
dc
dt= −ακ(cα − Cα
eq) c(0) = C0
• Exact solution for PDF
– Find c[κ(Y )], where Y is multivariate Gaussian
– Find pc(C) = (dy/dC)p(y)
0 0.2 0.4 0.6 0.8 1C
5
10
15
20
25
30
Prob
abili
ty D
ensi
ty F
unct
ion
pc(C
,t) t=0.01
t=0.1
t=0.25t=0.5
t=1
t=1.25
t=2
Effective (Upscaled) Rate Constant
• Find mean concentration c(t)• Define keff as the coefficient in
dc
dt= −αkeff
(cα − Cα
eq
)
0 2 4 6 8 10Time, t
0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
Ups
cale
d re
actio
n ra
te, k
eff
α = 1α = 2
• keff(0) = k
Perturbation Expansion for PDF
• Gaussian mapping, e.g., κ = f(Y ) where Y is Gaussian
• Small parameter σ2Y
• p = p(0) + p(1) + . . .
∂p
∂t= −∇ · (〈v〉p)− ∇ · 〈v′Π′〉 → ∂p(0)
∂t= −∇ ·
[〈v〉(0)p(0)
]• Randomness in initial and boundary conditions is easily incorporated
• Solution for the concentration PDF (a la Kubo expansion)
p(C; t) =dY
dC
∞∑n=0
σ2nY
(2n)!!δ(2n)(Y − 〈Y 〉)
Mean Concentration for Linear Kinetics (α = 1)
• Mild heterogeneity (σ2Y = 0.5)
0 2 4 6 8 10
Dimensionless time
0
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0.6
0.8
1
Nor
mal
ized
mea
n co
ncen
trat
ion
n = 0n = 1n = 2n = 3n = 4
Mean Concentration for Linear Kinetics (α = 1)
• Mild-to-moderate heterogeneity (σ2Y = 1.0)
0 2 4 6 8 10
Dimensionless time
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0
0.2
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0.6
0.8
1
Nor
mal
ized
mea
n co
ncen
trat
ion
n = 0n = 1n = 2n = 3n = 4
Mean Concentration for Non-linear Kinetics
• α = 2
• Mild heterogeneity (σ2Y = 0.5)
0 2 4 6 8 10
Dimensionless time
1
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1.8
2N
orm
aliz
ed m
ean
conc
entr
atio
n
n = 0n = 1n = 2n = 3n = 4
Mean Concentration for Non-linear Kinetics
• α = 2
• Mild-to-moderate heterogeneity (σ2Y = 1.0)
0 2 4 6 8
Dimensionless time
1
2
3
4
5
Nor
mal
ized
mea
n co
ncen
trat
ion
n = 0n = 1n = 2
LED Approximation of PDF Equations
• Transport equation
∂c
∂t= −∇ · (vc) + fκ(c) in R3
• Unclosed PDF equation
∂p
∂t= −∇ · (〈v〉p)− ∇ · 〈v′Π′〉 in R4
• Large Eddy Diffusivity (LED) closure
∂p
∂t= −∂〈ui〉p
∂xi+
∂
∂xj
[Dij
∂p
∂xi
]• “Dispersion” coefficient
Dij(x, t) ≈∫ t
0
∫Ω
〈v′i(x)v′j(y)〉G(x, y, t− τ)dydτ
Lagrangian-Eulerian Description
• Governing equations:
∂c
∂t= −∇ · (vc) + fk(c) ⇒ ∂Π
∂t= −∇ · (vΠ)
• Random Green’s function G(x, y, t− τ)
∂G∂τ
+ v · ∇yG = −δ(x− y)δ(t− τ)
• Explicit expression
G(x, y, t− τ) = [1−H(τ − t)]δ(y − xL), xL = x + v(t− τ)
• Mean Green’s function: G(x, y, t− τ) = 〈G(x, y, t− τ)〉
Effective parameters
0 0.2 0.4 0.6 0.8 1Normalized time
0
0.1
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0.3
0.4
Nor
mal
ized
disp
ersio
n co
effic
ient
ExponentialGaussianSpherical
0 0.2 0.4 0.6 0.8 1Normalized time
0.4
0.6
0.8
1
Nor
mal
ized
effe
ctiv
e ve
loci
ty
ExponentialGaussianSpherical
0 0.1 0.2Normalized time
0
0.5
1
1.5
2
2.5
Nor
mal
ized
disp
ersio
n co
effic
ient
ExponentialGaussianSpherical
0 0.1 0.2Normalized time
2
3
4
5
6
7
Nor
mal
ized
effe
ctiv
e ve
loci
ty
ExponentialGaussianSpherical
Conclusions
• Most physical systems are under-determined due to– Heterogeneity– Lack of sufficient data– Measurement noise
Wisdom begins with the acknowledgment of uncertainty—of the
limits of what we know. David Hume (1748), An Inquiry Concerning Human
Understanding