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    Shell Nigeria Graduate Training Programme Petrophysics

    Martey, A.O Univation2.1

    2 POROSITY

    In hydrocarbon reservoirs, the pore volume is available for storage of oil, gas, and

    water. The porosity or a rock is a measure of the amount of internal space that is

    capable of holding these fluids. Total porosity is defined as the, ratio of the volume

    of all the pores to the bulk volume of a material, regardless of whether or not all of

    the pores are interconnected. Quantitatively, the porosity istheratio of "the volume

    of the void space to the total volume of void space plus rock matrix. Porosity is

    normally expressed as a fraction or percentage of bulk volume.

    Porosity is

    ( )

    b

    mab

    b

    mab

    b

    p

    V

    WV

    V

    VV

    V

    V

    /=

    ==

    Vp = pore volume

    Vb = bulk volume

    Vma = volume of matrix minerals

    W = total weight of matrix minerals

    ?ma = matrix minerals density (weight per unit of minerals volume)

    Effective porosity is defined as the ratio of interconnected pore volume to the bulk

    volume of a material.

    The pore space available in a given rock depends on: the shape of the grains, the

    uniformity of the grains, the way in which they are arranged or packed, and the

    amount of cementing material between them. For instance, a "rock" made of

    cubically packed uniform spheres, without any cementing material would have a

    porosity of 48 per cent. The porosity is entirely independent of the size of the

    spheres.

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    A rock made of spheres is unknown, but the generalisation can be made that the

    more uniform the grains, the larger will be the porosity. For instance, if an actual rock

    is composed of grains with a wide range of grain sizes, then there will be a chance

    that the smaller grains will fill the interstices between the larger ones.

    Ordinary loose sand has a porosity of about 30%, but this drops to about 15% in

    sandstones, according to the degree of compaction and the amount of cementing

    material.

    Porosity of sandstones is controlled primarily by textural properties. These are

    1. Grain size

    2. Sorting

    3. Shape (sphericity)

    4. Roundness (angularity)

    5. Packing

    Of these, sorting and packing are of major importance, grain size, shape and

    roundness of relatively minor importance.

    Porosity in limestones is much more variable in magnitude than it is in sandstones.

    In some (reef-type) formations it is very high, in a few cases exceeding 50 per cent.

    However, in general the porosity of carbonate rocks is lower than it is in sandstones.

    Dolomites have normally good porosities.

    Identical spheres: A loose sand (uncemented, unconsolidated) can be represented

    by a particular packing of identical spheres. The porosity of such a packing can be

    calculated from its geometry. The calculation of porosity for a cubic packing is shownin Fig. 2.1 (48%). This packing is of course very unstable. Yet, porosities of 40 to 45

    per cent exist in unconsolidated sand formations (e.g. Venezuela).

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    Fig. 2. 1

    It is of interest to note that the porosity is independent of the size of the spheres.

    The tightest packing of identical spheres is rombohedral, with a porosity of 26%.

    Fig. 2.2

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    Porosity is a dimensionless ratio with a value between 0 and 1.0. It should be noted

    that it is often quoted, as a percentage (e.g. 26%) but must be entered in equations

    and calculations as a decimal fraction (e.g. 0.26).

    Grain size distribution: Identical spherical grains do not occur in nature, where

    ranges of grain need to be considered, and where the smaller grains tend to occupy

    the pore space between the larger ones. Porosity is therefore dependent on the type

    of packing and the grain size distribution (that is sorting).

    Wentworth designed a classification system defining grain sizes for siliclastics (Table

    2.1), and Archie for carbonates (Table 2.2).

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    Table 2.1: Siliclastics Table 2.1: Carbonates

    Crystal or grain size

    Category Median grain size in

    Microns

    Symbol Range in Microns

    Gravel Large

    Very Coarse Medium

    Coarse Fine

    Medium Vefy fine

    Fine Extremely fine

    400

    200

    100

    50

    Very fine Pore size

    Silt

    2000

    1000

    500

    250

    125

    62

    Symbol Range in

    microns

    B 2000

    1 Micron = 10-3 mm.

    Matrix texture:I = Compact

    II = Chalky

    III = Sucrose

    The grain size distribution of a sand or sandstone sample is determined by means of

    employing a vertical stack of sieves, the mesh size decreasing from the top

    downwards (Fig. 2.3).

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    The crushed sample is weighed and placed onto the upper sieve. Vibration of this

    sieve stack causes the grains to be rapidly distributed over the sieves. The

    cumulative percentage weight on each sieve is plotted against the mesh size (D) and

    a distribution curve is obtained (Fig. 2.4).

    Fig. 2.3. Assembly of sieve trays (finest screens at the bottom) for analysis of the

    grain-size distribution of sediments.

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    The degree of sorting, expressed by the Trask coefficient (So), is defined by the

    equation:

    So

    = (D25

    / D75

    )1/2

    in which

    D25 = grain diameter at 25% of sample weight (larger grains)

    D75 = grain diameter at 75% of sample weight

    Table 2.3 indicates the six sorting categories according to Trask.

    Fig. 2.4

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    Table 2.3

    Category Trask coefficient

    Extremely well

    Very well

    Well

    Moderately

    Poor

    Very poor

    1.00

    1.10

    1.20

    1.40

    2.00

    2.70

    5.70

    Actual porosity values: These may be as high as 45% in loose sands, and as low

    as 1 % instill prolific fractured carbonates.

    A common range ofporosities in sandstones and carbonates is as follows:

    recant sands (loose) 35 - 45%

    sandstones 20 - 35%

    tight sandstones 15 - 20%

    limestones (Middle East) 5 - 20%

    dolomites (Middle East) 10 -30%

    chalk (North Sea) 5 -40%

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    Some non-productive rocks also have high porosities. Shales, clays, and extremely

    fine-grained chalks fall into this category. They may have porosities 40% and higher.

    In general, a field appraisal classification of reservoir porosity is:

    5 10% poor

    10 20% good

    > 20% very good

    Porosity determination

    Buoyancy technique - Effective porosity

    Porosity is determined routinely on core samples as shown opposite in Fig. 2.5. Bulk

    volume, Vb , is determined by immersing in mercury. Because of the low atmospheric

    pressure, mercury does not invade the pore spaces, so the displacement of mercury

    (measured by Archimedes Principle of bouyancy) is equal to the bulk volume of the

    rock.

    Grain volume, Vg, is determined by immersion in chlorothene which, through wetting

    the grain surface, invades all pore spaces connected to the surface of the sample.

    Hence the volume of chlorothene displaced is equal to Vg. The reduction in weight isthe buoyancy, which is the product of the matrix volume (plus unconnected pore

    volume) and the density of the saturating fluid.

    Vg=( ) ( ) ( )

    densityechlorothen

    weightscaffoldCweightscaffoldsampleDweightsampleAchlochloair

    _

    _,_,_, ++

    From these two measurements, plus dry sample weight in air, porosity and grain

    density are calculated thus:

    b

    mb

    V

    VV =

    Matrix density ?m =mVvolumematrix

    airinWeight

    __

    __

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    Gas expansion method (Boyles Law Porosimeter)- Effective

    porosity

    An alternative for measuring grain volume is the Boyle's law method where Helium is

    used to invade the pore space (Fig. 2.6). The dry sample is inserted in the sample

    chamber and both chambers are evacuated. The two valves isolating the expansion

    chamber are then closed, and an initial pressure P1 is applied to the sample

    chamber. Then the valve on the left ofthe sample chamber is closed, and the valve

    between the sample chamber and the expansion chamber is opened. The pressure

    between two chambers is allowed to equalise to pressure P2.

    Fig. 2.5

    Fig. 2.6

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    Knowing Vb (again obtained by mercury immersion), Vs and Ve, the porosity can be

    calculated from the formula shown below.

    For ideal gases at constant temperature

    P1V1 = P2 V2

    Vs =volume of empty sample chamber

    Ve = volume of expansion chamber

    P1 [Vs - (Vb -Vp)] = P2 [Vs -(Vb -Vp) + Ve]

    P1Vs - P1Vb + P1Vp = P2Vs - P2Vb + P2Vp+P2Ve

    ( ) ( )

    ( )b

    seb

    b

    p

    VPP

    VPPVPVPP

    V

    V

    21

    21221

    +==

    Clearly only connected porosity is measured. If there is non-connected porosity, it

    will not be invaded by Chlorothene or Helium, and will be included in the grain

    volume with a consequent reduction in apparent grain density.

    Additionally Mercury may invade large vugs or fractures or even pore space in very

    coarse grained rock with a reduction in apparent bulk volume. This leads to a

    decrease in calculated porosity.

    Finally the porosity is that of a 'dry' sample dependent on the drying process

    particularly important in shaly sands.

    Pycnometer Method - Total Porosity

    The weight, W of the cleaned and dried core sample is obtained by weighing the

    sample in air. The Bulk Volume Vb is measured by immersion of the sample in

    mercury.

    A representative portion of the sample is then crushed to individual grain size. The

    crushed sample is weighed and its volume determined in a pycnometer by

    displacement of a non-wetting fluid.

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    The grain density ?g, will be the weight of the crushed sample divided by its volume.

    The grain volume, or matrix volume, of the original sample Vg, is calculated by

    dividing its weight by the grain density.

    The Total porosity is then equal to the bulk volume minus the grain volume divided

    by the bulk volume.

    = (Vb Vg) IVb or = [Vb - (W / ?g)] IVb

    This measurement gives the best results, but the disadvantage of this method is that

    the sample is destroyed in the process and no other measurements, such as

    permeability, can be taken on the sample afterwards.

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    IN UNCONSOLIDATED SANDS THE PORE SIZE IS ABOUT

    1/3 OF THE GRAIN SIZE. IN COMPACTED SANDS THE

    PORE SIZE IS ABOUT 1/10 OF THE GRAIN SIZE.

    DECREASE IN PORE DIAMETER IS THE RESULT OFCOMPACTION / DEPTH OF BURIAL

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