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Permeability
Saturation
- Special tests
Overburden pressure
Capillary pressure
Relative permeability
Wettability
Vb = Vg + Vp
IGNEOUS SEDIMENTARY METAMORPHIC
Rock-forming Source of
material
Recrystallization due to
Crystallization Sedimentation, burial
heat, pressure, or
(Solidification of melt) and lithification
chemically active fluids
The three major rock types are sedimentary, igneous, and metamorphic
rocks. Their classification is based on their origins.
Igneous rocks are formed from molten material which is either ejected from
the earth during volcanic activity (e.g., lava flows, and ash falls), or which
crystallizes from a magma that is injected into existing rock and cools
slowly, giving rise rocks such as granites. Igneous rocks are of minor
importance for oil exploration. Rarely, hydrocarbon is produced from
fractured igneous rocks.
Metamorphic rocks are formed by subjecting any of the three rock types to
high temperatures and pressures, that alter the character of the existing
rock. Common examples of metamorphic rocks are marble derived from
limestone and slate derived from shale. Due to the high temperature and
pressures there is very little organic matter or hydrocarbons in
metamorphic rocks.
Clastics
Carbonates
Evaporites
Grain-Size Classification for Clastic Sediments
Name Millimeters Micrometers
4,096
Boulder 256
Cobble 64
Pebble 4
Granule 2
Very Coarse Sand 1
Coarse Sand 0.5 500
Medium Sand 0.25 250
Fine Sand 0.125 125
Very Fine Sand 62
0.062
Coarse Silt 0.031 31
Medium Silt 0.016 16
Fine Silt 0.008 8
Very Fine Silt 0.004 4
Clay (modified from Blatt, 1982)
Average Detrital Mineral Composition
of Shale and Sandstone
Mineral Composition Shale Sandstone
Clay Minerals 60 (%) 5 (%)
Quartz 30 65
Feldspar 4 10-15
Carbonate 3 <1
Matrix
Sand (and Silt) Size Detrital Grains
Silt and Clay Size Detrital Material
Cement
Material Precipitated Post-Depositionally,
During Burial. Cements Fill Pores and
Replace Framework Grains
Pores
Voids Among the Above Components
COMPONENTS OF SANDSTONE
matrix CONSISTS OF QUARTZ, FELDSPAR, CEMENT AND CLAY
PORE
(QUARTZ)
CEMENT
(CLAY)
(FELDSPAR)
0.25 mm
PRIMARY (ORIGINAL) POROSITY
Developed at deposition
Typified by: Intergranular pores of clastics or
carbonates, AND Intercrystalline and fenestral
pores of carbonates
Usually more uniform than induced porosity
SECONDARY (DIAGENETIC)
Cementing materials
Overburden stress (compaction)
Vugs, dissolution, and fractures
In the geology section, we show core photographs with examples of porosity.
For now, it is useful to note these effects:
Vugs and fractures will contribute to porosity, but to understand their affect
on effective porosity requires careful study of cores and special logging
measurements.
ROUNDNESS AND SPHERICITY
OF CLASTIC GRAINS
Porosity
High
Low
Porosity
GRAIN PACKING IN SANDSTONE
Line of Traverse
(using microscope) 4 Types of Grain Contacts
Packing Proximity
Tangential Contact A measure of the extent to
which sedimentary particles
are in contact with their
Sutured Contact neighbors
Long Contact Packing Density
Cement
A measure of the extent to
which sedimentary particles
occupy the rock volume
Matrix
Concavo-Convex
(clays, etc.)
Contact
This Example
Packing Proximity = 40%
Packing Density = 0.8
(modified from Blatt, 1982)
CUBIC PACKING OF SPHERES
Porosity = 48%
Bulk volume = (2r)3 = 8r3
Matrix volume =
4 r3
3 volume
Pore volume = bulk volume - matrix
Pore Volume
Porosity
Bulk Volume
8 r3 4 / 3 r3
1 47.6%
8r 3
2 3
RHOMBIC PACKING OF SPHERES
Porosity = 27 %
Sorting (variable grain sizes)
SORTING
TYPES OF TEXTURAL CHANGES SENSED
BY THE NAKED EYE AS BEDDING
Sand
Shale Slow Current
Fast Current
Change of Composition Change of Size
River
Eolian
Beach
Fluvial
Change of Shape Change of Orientation
Change of Packing
PROGRESSIVE DESTRUCTION OF
BEDDING THROUGH BIOTURBATION
Regular Irregular Bioturbated Sandstone
Layers Layers (Whole Core)
Cementing materials
Oil Compaction
Stained Precipitation of Cement
Dissolution of Framework
Grains and Cement
The Effects of Diagenesis May
Enhance or Degrade Reservoir
Quality
Whole Core
Misoa Formation, Venezuela Photo by W. Ayers
DUAL POROSITY IN SANDSTONE
1. Primary and secondary matrix porosity system
2. Fracture porosity system
FRACTURE DISSOLUTION
PORE
PORE
(QUARTZ)
CEMENT
(CLAY)
(FELDSPAR)
0.25 mm
POROSITY IN SANDSTONE
Porosity in Sandstone
Pore Typically is Lower Than
That of Idealized Packed
Spheres Owing to:
Quartz Variation in Grain Size
Grain Variation in Grain Shape
Cementation
Mechanical and Chemical
Compaction
Pore
Throat Pores Provide the
Volume to Store
Hydrocarbons
Intergranular
Pore
Intergranular Pores
Microporosity Contain Hydrocarbon
Fluids
Significant Permeability
Reduction
Migration of Fines
Problem
Carter Sandstone
North Blowhorn Creek Oil Unit
Black Warrior Basin, Alabama, USA (Photograph by R.L. Kugler)
DISSOLUTION POROSITY
Partially Dissolution of
Dissolved Framework Grains
Feldspar (Feldspar, for
Example) and
Cement may
Pore Enhance the
Interconnected
Quartz Detrital Pore System
Grain
This is Secondary
Thin Section Micrograph - Plane Polarized Light
Avile Sandstone, Neuquen Basin, Argentina Porosity
Dissolution Pores
May be Isolated and
not Contribute to the
Partially Effective Pore System
Dissolved
Feldspar
Fabric
Selective
Fenestral Shelter Growth-Framework
Non-Fabric
Selective
Fracture Channel Vug
Moldic
Pores
Due to dissolution
Dolomite and collapse of ooids
(allochemical particles)
Connected pores
(Vp)
3. Pore volume
MATRIX VOLUME FROM
DISPLACEMENT METHOD
(Vp)
3. Pore volume
MATRIX VOLUME FROM GAS
EXPANSION METHOD
p1 V1 p2 V2
GAS EXPANSION METHOD TO
CALCULATE VMA
Place core in second cell, evacuate gas (air) from second cell
Open valve
GAS EXPANSION METHOD TO
CALCULATE VMA
Initial conditions
P1
V1 Core
Valve Evacuate
Cell 1 closed Cell 2
GAS EXPANSION METHOD TO
CALCULATE VMA
P1 Final conditions
P2
Core
Valve
Cell 1 open Cell 2
GAS EXPANSION METHOD TO
CALCULATE VMA
Vm = Vt - Vf
APPLICABILITY AND ACCURACY
OF MATRIX MEASUREMENT
TECHNIQUES
Displacement method - Very accurate when
core sample is crushed without destroying
individual matrix grains
Gas expansion method - Very accurate,
especially for samples with low porosities
Vp = Wsat - Wdry
fluid
2. Boyles Law:
(Gas expansion)
p1 V1 p2 V2
PORE VOLUME FROM
SATURATION METHOD
Measures the difference between the weight of a core sample
saturated with a single fluid and the dry weight of the core
Pore volume,
Wsat Wdry
Vp
f
ARCHIMEDES METHOD OF
CALCULATING
POROSITY A CORE SAMPLE
Vp
Porosity
21.3 cm3
= = 0.12 or 12%
179.0 cm3
Vb
APPLICABILITY AND ACCURACY
OF PORE VOLUME
MEASUREMENT TECHNIQUES
Saturation (Archimedes) method
Accurate in better quality rocks if effective pore
spaces can be completely saturated
In poorer quality rocks, difficult to completely
saturate sample
Saturating fluid may react with minerals in the
core (e.g., swelling clays)
LABORATORY METHODS OF
POROSITY DETERMINATION
2. Boyles Law:
(Gas expansion)
p1 V1 p2 V2
PORE VOLUME FROM GAS
EXPANSION METHOD
Initial conditions
P1
V1 Core
Valve
Cell 1 closed Cell 2
PORE VOLUME FROM GAS
EXPANSION METHOD
Final conditions
P1
P2
Core
Valve
Cell 1 open Cell 2
SUMMARY
1. Bulk volume
2. Matrix volume
3. Pore volume
use in determining the original hydrocarbon volume in place.
In case of large variation in the porosity vertically and no or small
variation horizontally or parallel to the planes, then the arithmetic
average or thickness-weighted average porosity is used:
Vp Vb Vma
Porosity
Vb Vb
V V V
b m p
V (V )
p b
V (1 )(V )
m b
m ( )(V )
Definition: Fraction, or percent, of the pore volume occupied by
a particular fluid (oil, gas, or water).
Is an intensive property
all saturation values are based on pore volume and not on the
gross reservoir volume.
- Direct Measurement
Core Analysis of samples obtained from formation of interest
in original state and measure saturations directly is ideal
- Indirect Measurement
Capillary Pressure Measurement
Well log analysis ( electrical conductivity primarily on water
saturation)
Factors affecting fluid saturations in cores:
Will obtain:
Note that:
k < 1 md poor
1 < k < 10 md fair
10 < k < 50 md moderate
50 < k < 250 md good
250 md < k very good
From Tiab
and
Donaldson,
1996
A
h1-h2
q
A
h1
h2
(Sand Pack Length) L
h1-h2
q
A
h1
h2
(Sand Pack Length) L
q
A
Substituting the relationship, q/A, in place of and
solving for q results in:
Condition must exist during measurement of permeability:
a) Horizontal flow.
b) Incompressible fluid.
c) 100% fluid saturation in the porous medium.
d) Stationary flow current, i.e. constant cross-section in flow direction.
e) Laminar flow current (satisfied in most liquid flow cases).
f) No chemical exchange or - reactions between fluid and porous medium
where the flow rate q and the pressure difference p are the
measured data. Permeability is found by plotting the
measured data as shown.
A cylindrical core sample is properly cleaned and all remains
of hydrocarbons are removed from the pore space. The core is
saturated with water and then flushed horizontally. The core
length is 15cm, its diameter is 5 cm and the water viscosity is
1.0 cp.
The average or representative permeability is k = 0.1 D or 100
mD
1. Measure inlet and outlet pressures (P1 and P2) at several
different flow rates
2. Graph ratio of flow rate to area (q/A) versus the pressure
function (P1 - P2) / L
3. For laminar flow, data follow a straight line with slope of k/
4. At very high flow rates, turbulent flow is indicated by a
deviation from straight line
By convention the unit for the permeability is called the Darcy.
Instead of the unit 1 Darcy, the 1/1000 fraction is used, which then is
called millidarcy (mD).
Darcys K was determined to be a
combination of
k, permeability of the sand pack
(porous medium, e.g. reservoir rock)
, viscosity of the liquid
Permeability is a derived dimension
From Darcys equation, the dimension of
permeability is length squared
q L L3 P T L 1 1
k ; 2 L2
A p T 1 1 L P
This is not the same as area, even though for
example, it is m2 in SI units
Given the pressure p1 and the gas rate q2, the mean pressure in the
core sample, p and the pressure drop across the core, Dp, are
calculated from the equation above. The gas permeability k is found as
a function of the mean core pressure.
Absolute gas permeability of the core sample is therefore found
as the asymptotic value of permeability, when p ! or more
conveniently, when 1/p ! 00
Assuming the used gases follow the ideal gas behavior (at low
pressures),
Mean pressure, Pm expressed as:
Gas flow rate is usually measured at base
(atmospheric) pressure Pb
Total flow rate qt is equal to the sum of the flow rates through
each layer or:
Combining the above expressions gives:
Some slides in this section are from NExT PERF Short Course Notes, 1999.
Some slides appear to have been obtained from unknown primary
sources that were not cited by NExT. Note that some slides have a notes section.
LABORATORY METHODS FOR
DETERMINING ABSOLUTE
PERMEABILITY
1 or 1 1/2
Plug
Slab Taken for
Most Common Photography
Description
Archival
Full Diameter
Heterogeneous
Whole Core
Heterogeneous
WHOLE-CORE METHOD
Different Unacceptable
Lithologies ~1 ft
kH ?
Require Or
Careful kH Full-
Suitable Diameter
Selection of kV kV
Suitable III IV V
Core Plugs kV
or Require Full kH Matrix
Whole-Core Diameter
`4 - 9
Only
Analyses Fracture
k and ?
Whole Core
Analysis
(2-3 ft)
Whole Core Photograph,
Misoa C Sandstone,
Venezuela
Photo by W. Ayers
LAB PROCEDURE FOR
MEASURING PERMEABILITY
q
A
k
Slope =
0
0 (p1 - p2)
L
ISSUES AFFECTING
LABORATORY MEASUREMENTS
OF PERMEABILITY
Core Handling, Cleaning, and Sampling
Fluid-Rock Interactions
Pressure Changes
Core Handling
Cleaning
Drying (Clay Damage)
Storage (Freezing)
Sampling
FLUID-ROCK INTERACTIONS
AFFECT MEASUREMENTS OF
PERMEABILITY
Fresh water may cause clay swelling, reducing
permeability
Tests may cause fines migration, plugging
pore throats and reducing permeability
Reservoir or synthetic reservoir fluids are
generally preferred
PRESSURES AFFECT
LABORATORY MEASUREMENTS
OF PERMEABILITY
Non-Darcy Flow
Some figures in this section are from Fundamentals of Core Analysis, Core Laboratories, 1989.
Some slides in this section are from NExT PERF Short Course Notes, 1999.
Some slides appear to have been obtained from unknown primary
sources that were not cited by NExT. Note that some slides have a notes section.
Air Permeability Measurement
Measurement of permeability in the laboratory is most
commonly done with air
Convenient and inexpensive
Problem: low values of mean flowing pressure
downstream pressure, patm
upstream pressure, just a few psi higher than patm
k A Tsc 1 2
q g, sc
L T p sc
2z
p1 p 22 )
g
For laboratory flow experiments we can assume T=Tsc and z=1
q g, sc
k
A p12 p 22
)
g psc 2L
For Darcy flow, plotting (qg,sc psc)/A vs. (p12-p22)/(2L) results in
straight line.
line passes through origin [when qg,sc =0, then (p12-p22)=0]
slope = k/ g
behavior departs from straight line under turbulent flow conditions
(high flow velocity)
NON-DARCY FLOW - TURBULENCE
Darcy Non-Darcy
flow flow
q psc
A
k
Slope =
0
0 (p12- p22)
2L
Non-Darcy Flow - Forchheimer Equation
Slope = [(bg,sc)/(gA)]
Intercept = [1/kabs]
qg,sc
Non-Darcy Flow - Forchheimer Equation
Non-Darcy Coefficient, b, is an empirically determined
function of absolute permeability
For Travis Peak (Texas)
NOB=Net
Overburden
Conversion Factors
for
Oilfield Units
Need for Unit Conversions
Petroleum Engineers must be able to work with various
unit systems
International scope of industry
Unit systems used varies geographically
Team members may not all be located in same geographical location
Joint ventures between companies
Particular units may be required at your location
Legislated units for reporting and regulatory compliance
Company protocol
Oilfield Units
Oilfield units are non-coherent
Newtons 2nd Law (F=ma)
SI: Force (Newton) is a derived unit to make equation coherent
USCS: Mass (slugs) is a derived unit to make equation coherent
AES, Oilfield Units: A unit conversion constant required (F=ma/gc )
Darcys Law
Darcy units: Permeability is a derived unit to make equation coherent
SI: coherent (permeability unit is m2 )
Oilfield Units: A unit conversion constant is required
The constant may include geometry terms (integrated form)
For gas flow, the constant may include standard temperature and pressure,
even for Darcy and SI units
q C k d
vs
A ds
Learning Objectives
Deriving unit conversion constants
Given
A physical relationship expressed as an equation, using coherent units or
with a correct conversion constant supplied
and appropriate unit conversion factors between unit systems
Find
The required unit conversion constant (including its units) to express the
equation in a different unit system
q
kA
p)
L
where,
q cm3/s
k darcies
Acm2
Dp atm
cp
L cm
q
CkA
p)
L
where,
q bbl/D
k millidarcies
Aft2
Dp psia
cp
L ft
q
kA
p1 p2 )
L
We can determine how x p(x)
pressure varies along kA
the flow path, p(x), by q ds dp
considering an arbitrary 0
p1
point, 0x L q x
Integral from 0x p(x) p1
kA
OR, equivalently
L p2
kA
We
A
q could alsoLintegrate
2
q ds dp
xL 1 x
p(x)
q (L x)
p(x) p2
kA
Pressure profile is a
linear function for
homogeneous properties
slope depends on flow rate p1
p(x)
p
A
p2
q L 2
1
0
0 x L
x
There are three simple permeability-averaging techniques that
are commonly used to determine an appropriate average
permeability to represent
an equivalent homogeneous system. These are:
Weighted-average permeability
Harmonic-average permeability
Geometric-average permeability
Permeability varies across several
horizontal layers (k1,k2,k3)
Discrete changes in permeability
h h1 h 2 h 3 h i
Same pressure drop for each layer
p1 - p2 p p1 p2 p3
Total flow rate is summation of flow rate for all layers
q q1 q 2 q 3 q i
Average permeability results in correct total flow rate
kwh
q p ; A w h
L
Substituting,
kwh k1 w h1 k2 w h2 k3 w h3
q p p p p
L L L L
Rearranging,
k
k i hi
h
Average permeability reflects flow capacity of all layers
Permeability varies across several
vertical layers (k1,k2,k3)
Discrete changes in permeability
L L1 L2 L3 Li
Same flow rate passes through each layer
q q1 q 2 q3
Total pressure drop is summation of pressure drop across layers
p1 p2 p1 p2 p3 pi
Average permeability results in correct total pressure drop
q L
p1 - p2 ; A wh
kwh
Substituting,
q L q L1 q L2 q L3
p1 - p2
k w h k1 w h k 2 w h k 3 w h
Rearranging, L
k
Li
k p1
i
If k1>k2>k3, then k
p
Linear pressure profile in each layer p2
0
0 L
x
q k dp
Review, Darcys Law: vs
horizontal flow (=p) A ds
q k
dr dp
2 rh
rw pw
1 2 kh
q q dr dp
re
r pe
q
2 kh
p e p w )
rw re
ln(re /rw )
We can determine how rw
1 2 kh
pw
q ln(re /r)
p(r) p e
2 k h
Pressure profile is a
linear function of ln(r)
for homogeneous
properties pe
slope depends on flow rate
p(r)
p
pw
q
0
rw r re
ln(r)
rw re
Permeability varies across several
(3) horizontal layers (k1,k2,k3)
Discrete changes in permeability
h h1 h 2 h 3 h i
Same pressure drop for each layer
pe - pw p p1 p2 p3
Total flow rate is summation of flow rate for all layers
q q1 q 2 q 3 q i
Average permeability results in correct total flow rate
2 k h
q p
ln(re /rw )
Substituting,
2 k h
q p
ln(re /rw )
2 k1 h1 2 k 2 h 2 2 k 3 h 3
p p p
ln(re /rw ) ln(re /rw ) ln(re /rw )
Rearranging,
k
k i hi
h
re rw r1 r2 ri
Same flow rate passes through each layer
q q1 q 2
Total pressure drop is summation of pressure drop across layers
pe p w p1 p2 pi
Average permeability results in correct total pressure drop
q ln(re /rw )
pe - p w
2 k h
Substituting (rw=r1, r2 ,re=r3),
q ln(re /rw ) q ln(r2 /rw ) q ln(re /r2 )
pe - p w
2 k h 2 k1 h 2 k 2 h
Rearranging,
ln(re /rw )
k
(ln(ri 1/ri )
All Layers ki
A hydrocarbon reservoir is characterized by five distinct
formation segments that are connected in series. Each
segment has the same formation thickness. The length and
permeability of each section of the five bed reservoir are given
below: