Summary
For decades the effect of physical dispersion (in-situ mixing) in porous
media has been of interest in reservoir engineering and groundwater hydrology.
Dispersion can affect the development of multicontact miscibility and bank
breakdown in enriched-gas drives and miscible solvent floods of any mobility
ratio.
The magnitude or extent of dispersion is quantified by the rock property
physical dispersivity, α, which is on the order of 0.01 ft for
consolidated rocks and several times smaller for sandpacks, as found in many
laboratory measurements.
Numerical studies of the effect of dispersion on enriched-gas drives and
field tracer tests often use input values of a scale-dependent dispersivity 100
to 1,000 or more times larger than ~0.01 ft. These large-scale dependent
dispersivity values stem from large apparent dispersivities
(αa) determined by matching the 1D convection/diffusion (C/D)
equation to production-well-effluent tracer-concentration profiles observed in
field tracer tests.
A scale-dependent dispersivity can be used only as a fitting factor to match
or explain the effluent profile of a single producer at a fixed distance from
an injector. It cannot represent physical dispersion to justify the conclusions
reached by its use in simulations of enriched-gas-drive, field-tracer-test, or
other reservoir displacement processes. It has no predictive value in any
numerical simulation.
The scale-dependent apparent dispersivities reflect conformance or other
behavior not governed by the 1D C/D equation and should not be used to justify
large dispersivities as input to numerical studies. This paper shows that large
apparent dispersivities observed in field tests can result with physical
dispersivity no larger than the ~0.01-ft laboratory-measured value.
Heterogeneity alone (no physical dispersivity or molecular diffusion) causes
no in-situ mixing and cannot explain observed large apparent echo-test
dispersivities. Large apparent dispersivities for two reported echo
(single-well inject/produce) tracer tests are shown to result from a model with
drift alone and no dispersion.
The widely reported scale dependence of apparent dispersivity is a simple
and necessary consequence of mis-applying the 1D C/D equation, with its single
parameter of Peclet number, L/α, to conformance it does not
describe. The conformance portion, αac, of apparent
dispersivity, αa, is scale-dependent, but physical
dispersivity is a rock property independent of scale and time. The value of
αa approximately obeys an additive dispersivity principle,
αa≈α + αac, where
αac is dispersivity representing conformance and
αac>>α in field displacements.
© 2009. Society of Petroleum Engineers
View full textPDF
(
5,858 KB
)
History
- Original manuscript received:
7 June 2007
- Meeting paper published:
26 September 2004
- Revised manuscript received:
6 March 2008
- Manuscript approved:
27 September 2008
- Published online:
2 March 2009
- Version of record:
26 February 2009