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no CO2 emissions
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13 storage sites in 9 states Perpetual carbon dioxide storage rights at ~500k private acres 10 Gt+ of CO2 storage capacity equivalent to 30 years of emissions from 15% of the US coal fleet
MADRONE CAPITAL
Outline
Take groups of fluid molecules (the continuum approach) Apply a stress or shear to them
2.
3.
Ask yourself: How will the parcel of fluid respond? Will it deform? Expand? Move out of the way?
Five unknowns: density (r), pressure (p), velocity (u = [u,v,w]), Five equations: mass conservation (continuity) momentum conservation (in [x, y, z]) equation of state (relates r to p, and other state variables)
Acknowledgement: these slides are based on course notes by Prof. H.A. Stone.
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4.
5.
p(x + x; t) (x + x; t) u(x + x; t)
flow
@ @t ( A x)
= ( u A)jx ( u A)jx+x
@ @t
In the limit of small Dx, and for flow in 3-D, this becomes:
+ r ( u) = 0
p(x + x; t) (x + x; t) u(x + x; t)
flow
@ u
@t
+u
@u @x
@p = @x
p(x + x; t) (x + x; t) u(x + x; t)
flow
@ u
@t
+ u ru = f + r T
T = pe I +
stresses that DO depend on u
@ u
@t
+u
@u @x
= 0; so 0 = g rp
before.)
@p = @x
p(x + x; t) (x + x; t) u(x + x; t)
flow
@ u
@t
+ u ru = f + r T
T = pe I +
stresses that DO depend on u
Viscosity is just the coefficient that relates stress to velocity gradients. Thus, in its most common form, the Navier-Stokes equations are:
@ @t
(ut + u ru) = rp + r2 u + g
+ r ( u) = 0
Navier-Stokes in words
(ut + u ru) = rp + r2 u + g
fluid particles are neither generated or destroyed, they just move around fluids will move when subjected to pressure gradients and external foces, but viscosity will always resist the fluid motion
@ @t
+ r ( u) = 0
Simple (but very relevant!) application why you should watch your cholesterol
ut = 0 = constant; ) r u = 0 u = u ) r u = du = 0 ) u ru = 0 dx
)
dp dx
r dp 2 dx , and again:
dp Q = 8 dx R4
du = r dr 2 dp 2 r u = R dx 1 R2 4
d r dr
u
p1
viscosity m
p2
2 dp r u = R dx 1 R2 4
2
Darcys Law
u
p1
viscosity m
permeability k porosity f L
p2
dp u = k dx
Outline
pg ; g ; g
CO2
pw; w; w
water
(affects capillary pressure, and relative permeability) (affects buoyancy) (affects relative permeability) (affects relative permeability)
ug =
k kr;g g
(rpg + g)
dp u = k dx )
w; w
water
uw =
ug =
k kr;w w
rPw =
k kr;w w
(rpw g)
k kr;g g
rPg =
k kr;g g
(rpg + g)
= w g
pg pw = pc 2 Rpore
How do we go from flow at the pore scale, to flow at the reservoir scale? The (imperfect, yet sort of useful) answer: relative permeability. It is impractical to know and model all pores and channels perfectly.
Relative Permeability
Bachu & Bennion, Env. Geo. 54, (2008)
imbibition (post-injection)
Capillary Trapping
http://www2.bren.ucsb.edu/~keller/micromodels.htm
0.5
kr,g 0 1 Sw 0.5 1 0
Sg
Capillary Pressure
Water Saturation, Sw
w; w
water
pg pw = pc 2 Rpore
Outline
5 degree dip 0.5 Mt/yr for 15 years ~ 1,400 m depth T = 40oC Salinity = 15,000 ppm TDS Grid block sizes: 100 m x 100 m x 10 m
Parabolic anticline 0.5 Mt/yr for 15 years ~ 1,450 m depth T = 40oC Salinity = 15,000 ppm TDS Grid block sizes: 100 m x 100 m x 5 m
15 years
50 years
10 years
15 years
50 years
Effect of Heterogeneity
Permeability Model
mobile
mobile mobile
Area of Review is defined as the area within which the CO2 sequestration project could cause endangerment to a USDW.
Endangerment comes from presence of mobile CO2, and from increased pressure that can push brine into the nearest USDW through leakage pathways. MESPOP maximum extent of separate phase or pressure
Conservatively, guidance recommends assuming that there is an open borehole somewhere, and calculating the maximum pressure rise in the injection reservoir that would just prevent brine from reaching the USDW through that open borehole....
rw
USDW
D
H
caprock injection formation
rb
Pressure rise required to push column of brine up from injection formation to USDW (assuming open frictionless borehole, and initially hydrostatic pressures):
Dp = (rb-rw) g H
or, in normalized form:
rw
D H USDW caprock
rb
injection formation
1. High salinity & large H/D (Illinois) rb = 1200 kg/m3, H = 2000 m, D = 2050 m Dp/p = 19.5%
2. Low salinity & small H/D (North Dakota) rb = 1005 kg/m3, H = 1000 m, D = 1500 m Dp/p = 0.3%
1.
High salinity & large H/D (Illinois) 3, H = 2000 m, D = 2050 m rb = 1200 kg/m Dp/p = 19.5% Low salinity & small H/D (North Dakota) 3, H = 1000 m, D = 1500 m rb = 1005 kg/m Dp/p = 0.3%
2.
Questions?
Contact Information:
Ernst A. van Nierop ernst@c12energy.com tel: 617-849-8006
Additional Slides
Continuum = averaging. This is OK if the length scale and time scale of the averaging is much smaller than the scales of the motion we are interested in.
If the flow occurs over the macro length scale, it will be described well by fluid properties that are averaged on a smaller ave scale. This length scale needs to be larger again than the molecular scale on which stuff actually happens.
1 m3 contains about 3 1010 water molecules or 1010 benzene mols., or 107 gas molecules. Even if it is 100 times smaller on each side (10 nm 10 nm 10 nm), there are still 104 molecules in a liquid. Typical collision time scales are 1012 s, so the time scale is not a problem in most cases.
Statistical physics tells us that thermal fluctuations scale as dN N1/2 so if we require the average to work well, i.e. be within 10% of the fluctuations, then we require dN/N N-1/2 <0.1; or N 100 particles!
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