Summary
The problem of CO2 sequestration in geologic formations is
analyzed from a fundamental perspective. In order to clearly understand the
first order behavior of the system, the mechanisms of trapping, dissolution and
chemical reactions are not accounted for. The analysis is concerned with the
post-injection period when the CO2 plume rises due to buoyancy.
Characteristics of the plume for a 1D problem show that a pair of shocks moving
in opposite directions is produced at the top end. The downward moving shock
interacts with the bottom end of the plume resulting in a decrease in the
maximum value of the CO2 saturation. High accuracy numerical
simulations are employed to understand the 2D mechanisms of plume evolution in
terms of the viscosity ratio and the capillary number. 2D results show that the
plume rises to significantly lower depth,in shorter times, as compared to the
1D problem. This behavior is governed by the 2D velocity field around the plume
that additionally leads to spanwise wave interactions and results in a faster
decrease of the maximum CO2 saturation. The initial dimensions of
the plume have a strong influence on the time scales of the wave interactions.
The maximum upward velocity that is generated due to buoyancy is closely
related to the maximum saturation and decays rapidly to very small values with
a decrease in saturation. In the case where the viscosity of CO2 is
a tenth of the viscosity of the surrounding fluid, the plume rises up about 500
m in 700 yrs. Our results provide an upper bound on the maximum rise distance
and the sequestration time for the problem involving trapping and dissolution.
Comparison with experimental results show that the buoyancy velocity obtained
from our results is of the same order as observed in the experiments.
Introduction
The behavior of two-phase flow in porous media under conditions of unstable
density stratification is an important and challenging problem applicable to
many practical settings of interest. Particularly,the dynamics of two-phase
immiscible flows that are gravitationally unstable play a central role in the
area of carbon dioxide storage in depleted reservoirs and saline aquifers. The
important issue in this regard is the understanding and prediction of the fate
of CO2 over a time period of geological scale (Bachu et al. 1994).
The success of CO2 sequestration operations in subsurface geological
formations is critically linked to the ability of the storage site to sequester
the gas indefinitely. The main mechanisms of sequestration are microscopic
residual trapping, dissolution of gas into brine, and chemical fixing of carbon
into the rock (Gunter et al. 1997). Various time scales as well as the nature
of the storage site determine the relative importance of these mechanisms.
The sequestration process can be broadly classified into three phases
(Ennis-King and Paterson 2005). Namely, the injection phase where
super-critical CO2 is injected into the site. This is followed by
the post-injection period where the gas rises as a buoyant plume. Residual
trapping and dissolution will be of primary importance in this stage. The final
stage is thought to be governed by dissolution driven gravitationally unstable
flows (Riaz et al. 2006) as well as chemical reactions of CO2 with
the porous rock. During the initial stage, the density and viscosity of the
injected gas are less than the resident brine; therefore, the flow can
potentially become unstable hydrodynamically (Riaz and Tchelepi 2007) due to
unfavorable contrasts of density and viscosity. The extent of the initial
injection period is determined by the amount of carbon dioxide that can be
stored in a given reservoir; however, this period is expected to be much
shorter than the subsequent post injection period. The modeling of the
injection process, which is based on the relative permeability formulation of
the Darcy equations, is thought to be well developed for drainage type
displacements that occur during this phase (Kumar et al. 2005). Most of the
main trapping mechanisms are either unavailable or are relatively less
important during the initial period. For example, residual trapping does not
take place during drainage while chemical trapping occurs over much larger time
scales. Viscous instability at the macroscopic scale is also a possibility
(Riaz and Tchelepi 2006).
Our understanding of the evolution of the CO2 plume during the
post injection period is incomplete. It is during this stage that the processes
of residual trapping and dissolution are expected to play a primary role. While
in general one can expect the plume to rise due to buoyancy, the particular
mechanisms of transport are in the initial stages of investigation (Wood et al.
2004; Stohr and Khalili 2006; Tokunaga et al. 2000). For example, what is the
most appropriate model for the flow; is the relative permeability model
appropriate, or given the extremely small capillary numbers, should the
invasion percolation model be used (Yortsos et al. 2001)? Regardless of which
model is used, the main questions that need to be addressed are: how far can
the plume rise; what is the velocity of rise, and how far does the plume spread
during its ascent? The last issue is important from the point of view of
dissolution which occurs immediately when the gas comes into contact with
unsaturated brine. However, because the saturation threshold of brine is small,
a continuous supply of fresh brine around the buoyant plume can increase
dissolution significantly. In this investigation we attempt to understand the
dynamics of the CO2 plume during the period immediately following
the injection phase. We use the Darcy relative permeability model to analyze
the dynamics governing the natural convection of the buoyant plume and provide
some preliminary estimates of how far and how fast will the plume rise. In
order to focus on the primary characteristics of transport governed by the
Darcy model, we carry out the analysis for homogeneous rocks, without residual
trapping and dissolution. Hence, the first order behavior of the system will be
considered as a primary guide to subsequently develop a better understanding of
more complex processes. A sketch of the CO2 plume is shown in Fig.
1. The non-wetting gas phase is immersed in brine which is the wetting phase. A
buoyancy force per unit volume FB results in upward motion
with velocity proportional to UB ,inducing a downward flow of
brine around the plume.
© 2008. Society of Petroleum Engineers
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History
- Original manuscript received:
28 June 2006
- Meeting paper published:
24 September 2006
- Revised manuscript received:
8 November 2007
- Manuscript approved:
12 November 2007
- Version of record:
20 September 2008