Beruflich Dokumente
Kultur Dokumente
CHAPTER 4
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
4.4.8.1 Damage due to the acid reaction, acid additives or reaction by-
products.................................................................................4-65
4.4.8.2 Damage caused by the treatment operation..........................4-68
4.4.8.3 Minimisation of damage during acidisation............................4-68
4.4.9 Formation Damage during Fracturing Operations .........................4-69
4.4.9.1 Impairment of the propped fracture .......................................4-69
4.4.9.2 Permeability impairment of the formation at the fracture face4-70
4.4.9.3 Minimisation of damage during fracture treatments...............4-70
CHAPTER 4
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
4.1 Introduction
During the life of a well, a number of operations are conducted within it from
the initial drilling, through the production and workover phases to final
abandonment. The production capacity of the system is extremely vulnerable
to impairment due to a variety of causes. The viability of a well in economic
terms depends crucially on generating revenue and maximising the next
present value of production.
Ke • h Kr • Ka • h
or
µf µf
has been altered. This more general consideration of damage will be evident
when one or more of the following is altered:
CHAPTER 4 Page 4 -1
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
From radial flow theory, it is possible to consider the flow through a composite
reservoir with damage, as the combined flow through two reservoir sections in
series i.e.
where Pe, Prd and Pwf are respectively the pressures at the outer boundary of
the reservoir re, the outer boundary of the skin zone at radius rd and at the
wellbore rw.
• The damage will be dependent on the total volume of fluid and damage
material injected or flowing into the reservoir damage zone.
(2) Substantial depth of damage must be avoided at all costs as the effects
can be very serious and such damage is not easily alleviated, e.g.
perforating will not penetrate beyond say 2ft and hence the perforation
could remain within the damage zone.
CHAPTER 4 Page 4 -2
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
CHAPTER 4 Page 4 -3
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
The solid constituents of the invading fluid and the reservoir rock
a fluid : fluid
or, a fluid: solid
or, a solid: solid
i.e. formation damage results in a reduction in the desired mobility of the fluid
as depicted in Figure 3.
This class of mechanism is perhaps the most varied, but a number of the
mechanisms will be discussed in turn.
The migration of solids either into or from within the porous media, can result
in the solids plugging either the pore throat or pore space. In the case of the
former, the flow area of the pore throat represents the minimum cross
sectional flow area and hence a major constriction to fluid flow. The
movement of solids within a fluid can lead to their arrival at a pore throat
through which they are unable to pass either because ofthe individual particle
size or shape alignment preventing its passage through the pore-single
particle bridging (Figure 4). Physical interaction between particles which
results in multiple particle bridging (Figure 4).
CHAPTER 4 Page 4 -4
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
CHAPTER 4 Page 4 -5
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
Single particle bridging is most likely to occur at the surface of the porous
media, whilst multiple particle bridging can occur both on the external surface
or within the pore space (Figure 5). Further, for a finite amount of particulates,
single particle bridging will obviously have a more serious impact on fluid
transmissibility than multiple particle bridging.
The complexity of the pore structure was highlighted by Maly who claimed that
in a 1 inch square sample of sandstone the number of pore exits was of the
order of 3000. He subsequently referred to the formation as “a most efficient
depth filter” for the entrapment of particulate material.
There are tow types of particles, namely; inorganic such as silica, silts, etc.,
and organic particles such as bacteria and fungi.
The source of particles in well operations varies from the drilling mud with a
relatively high solids content but a limited volume of fluid which enters the
formation, to injection water which contains a low concentration of fine
particulates but is injected in substantial quantities into the reservoir. Hence
consideration must be given to not only the size and shape of particulates,
and their concentration but also the cumulative solids injected into the pore
space.
The differential pressure provides the driving force or energy potential for the
flow of fluids into the reservoir from the wellbore.
The injection of a slurry or suspension into a porous media gives rise to solids
bridging and deposition both on the surface and within the pore space
(Figure 6). Particles which are larger than the pore throat size will be unable to
enter the pore space and will therefore bridge externally on the surface of the
porous media. Similarly particles of a certain size range although much
smaller than the pore throat size will bridge across the pore throat in
combination with other particles. (Figure 7) The deposition of particles in this
way will give rise to an external filter cake. For drilling fluids the permeability of
a filter cake deposited on a porous surface is of the order of 10-3 – 10-6 md
and is therefore several orders of magnitude lower than the permeability of the
porous media.
CHAPTER 4 Page 4 -6
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
CHAPTER 4 Page 4 -7
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
CHAPTER 4 Page 4 -8
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
Smaller particles which can enter the pore space will migrate into the porous
media and subsequently plug an inside pore throat or deposit within the pore
space by sedimentation (Figure 8). The combination of these two inside
plugging mechanisms results in the formation of an internal filter cake. Since
the borehole is surrounded concentrically by the formation the velocity of the
fluid flowing through the pore space will be governed by radial flow and hence
be a function of the distance from the wellbore. Then the sedimentation forces
on particles will increase as the distance from the wellbore increases.
The size of particulates which can enter a pore space is dependent on the
size, shape and packing of the rock grains. If we can assume a homogeneous
rock system then if the grains are packed in a square fashion the diameter of
the pore between the grain is 35% of the grain diameter. If, however, the
grains are packed hexagonally the pore diameter is only 15.47% of the grain
size (Figure 10).
Further Coberly and Wagner, from work on gravel packing suggested that
assuming spherical particles and bridging at a round orifice, then for bridging,
the ratio should be:
dpart ≥ 0.5pore
However, these approaches are somewhat simple and theoretical since they
do not take account of heterogeneity in size, shape and packing nor do they
consider realistically interference bridging.
Particles with a diameter greater than or equal to 1/3rd of the mean pore throat
size will not pass through it and thus cause external bridging.
Particles with a diameter greater than or equal to 1/7th of the mean pore throat
size enter the porous media but may bridge internally.
Particles with a diameter equal to or less than 1/10th of the mean pore throat
will pass through the porous media unhindered.
CHAPTER 4 Page 4 -9
Formation Damage
Curtin University of Technology Master of Petroleum / Petroleum Well Engineering
Department of Petroleum Engineering Remedial, Stimulation & Intervention Operations
Maly suggested that the 1/3rd rule does not hold at low flowrates. This
presumably suggests that at low rates the impact of sorting/deposition allows
individuals particle alignment/alignment to the pore throat.
These bridging rules are still widely used within the industry, normally in a
reverse manner, to design fluids which will create primarily an external filter
cake and hence limit the volume of invasion fluid.
The removal of these particulates from porous media by backflowing has been
studied. It has been recognised that lower flow rates does not favour the
removal of particles and that in fact optimum clean up is associated with an
intermediate flowrate.
(1) Minimise or reduce particle invasion by limiting the fluid volume which
enters this pore space,
and/or
• Particle deposition within the pore space around the perforation tunnel
Thus for the perforated completion the number of pore throats available
for plugging are <25% of the comparable open hole completion and
hence the statistical possibility of damage and its resultant effect are
much greater in a perforated completion.
• differential pressure )
• base fluid viscosity ) control the invasion leak-off rate
• formation permeability )
• particle size
• particle size distribution
• particle shape
• particle concentration
• pore size
• pore shape
• pore size distribution
However, once particulate invasion has occurred it is difficult to
alleviate.
Although the majority of sandstones contain clays, they are normally referred
to as being clean where they contain say less than 5% clay in their
mineralogy. “Dirty sandstones” commonly contain more than 5% clays and
can on occasion contain more than 20%.
The combination of these units can result in several different forms of clay
structure each also having different mineralogical composition and
characteristics.
Elemental substitution can take place within the matrix in the form of
Fe++/Mg++ for Al+++ in the octahedral sheet and Al+++ for Si++++ in the
tetrahedral sheet. This substitution gives rise to a negative charge on
the structure to a value of –1 for 1.5 unit crystals. This negative charge
imbalance can be alleviated by the adsorption of cations such as H+,
K+. Na+.Ca+ or Mg++ on to the outer surface of the clay molecule. The
molecular bonding within the crystal is weak and can allow water
molecules to move into the space between clay crystals giving rise to
molecular separation and the resultant expansion. The basic width of
the unexpanded montmorillonite molecule is of the order of 8-10 A but
this can be more than doubled by water adsorption and molecular
expansion.
It is clear that the charge imbalance on clay molecules gives rise to an ability
for cation exchange on the clay surface. Since montmorillonite has the highest
charge imbalance it has the greatest capacity to absorb cations. It is also the
clay which possesses the greatest capacity to expand volumetrically, if water
molecules are absorbed between the platelets. Other clays such as illite and
kaolinite can expand but only slightly.
If clay expands then, depending on the type of clay, the following may result:
• The expansion of the clay may lead to its mobilisation within the
pore space whereupon it can migrate and plug the pore
space/throats.
Jones considered tests on clay swelling and concluded that the degree of
swelling depended not only on the type of cation but also the ionic
concentration. He suggested that if a weak salt solution is used, it forces its
way into the clay lattice in an attempt to dilute the atmosphere of cations
surrounding each platelet
Thus if a solution containing Na+ contacts a calcium montmorillonite, it may
disperse if the Ca++ concentration is too low. Therefore, it is recommended
that the invading solution should contain about 10% of its dissolved salts as
Ca++ or Mg++. If the Ca++ concentration is high enough then clay molecules
may flocculate but the permeability will be relatively unaffected. The type of
cation is most important. For example, contacting a sodium montmorillonite
with a solution containing Ca++ salts will allow the Ca++ salts to effectively
replace the Na+ because of the charge imbalance. However, Na+ salts will not
easily replace Ca++ ions and in fact K+ ions are more effective than the Na+.
In Figure 20 it can be seen that the Ca montmorillonite is particularly stable in
that if possesses 4 layers of water under a range of ionic conditions. However,
the sodium and potassium based clays are much more greatly affected.
The manner in which a salt solution contacts a clay may also affect the degree
of adsorption and swelling. Jones suggested that the more abrupt the change
in salinity between the indigenous water around the clay and the injected
water, the greater would be the extent of swelling and dispersion. It is
therefore clear that a shock change in salinity would be detrimental.
The pH of the invading fluid can also affect the degree of swelling. If the pH of
the fluid is increased, the degree of clay destabilisation increased resulting in
clay particle mobilisation. This was further highlighted by Veley who observed
that whilst rock may exhibit increased permeability to NaCl and KCl brines
compared to CaCl2, if the pH of all the solutions was adjusted to 7 before
injection, the permeability to all the solutions was similar. It should be noted
that CaCl2 has a much higher pH than NaCl/KCl. The effect of pH may be
particularly prevalent for cementing operations.
The influence of water saturation in the pore space is crucial to the majority of
fines mobilisation and plugging mechanisms. This has been clearly shown by
Muecke (Figures 28, 29).
Fines of mixed wettability are constrained to the oil/water interface if they are
mobile (Figure 30).
Not all fines are indigenous but they can be created by a number of
mechanisms associated with normal production or injection operations:
Inorganic salts are soluble in water to varying degrees and the level of
solubility depends not only on the ionic concentration but also on the pressure
and temperature. For a pure salt solution, the salt concentration can be
progressively increased and the material will go into solution until a solubility
limit is exceeded whereupon the solution becomes supersaturated and the
salt may exist as a crystalline phase. The solubility limit is affected by a large
number of factors including the salinity and concentration of other salts.
Thus as inorganic salt may be deposited when the ionic balance of a solution
is disturbed either by decreasing pressure and temperature or by mixing with
a fluid with a different salt concentration.
The deposition of such scales results in a plugging of the flow channels either
in the pore space or in the tubing. The extent of plugging can be substantial
and result in a severe loss in productivity/injectivity. However, this loss in
productivity is not easily traced back to scale formation unless:
• A theoretical assessment of salt solubility predicts its likely
occurrence.
• Physical blockage of the tubing or flowline can be related to
either increased pressure tubing loss, or by the inability to pass
wireline tools down the string, or samples of scale are retrieved
from the wellbore or processing system and analysed.
In general terms given the difficulty of removing scale which has formed in the
tubing, separators, or in the formation, the former predictive approach has its
merits.
Scale deposition can also occur in a range of operations where either fluid
mixing is generated or the flowing conditions promote supersaturation:
• Mixing of formation water with injected seawater
• Mixing of cement filtrate with connate water in the reservoir and
the associated changes in pH
• Dehydration of connate water and consequent salt concentration
in gas wells
• Alteration in salt concentration as a results of the by products of
reactions occurring in acid treatments.
A large variety of salts can exist. The simplest salt system is NaCl which can
build up in the near wellbore area of the reservoir. However, the deposition is
readily dissolved by backwashing the reservoir with water. Of more
importance are the scales which deposit as a crystalline film and mainly
comprise the sulphate and carbonate salts of various minerals.
Calcium Carbonate CaCO3 is perhaps one of the most frequently
encountered scales but is readily soluble in HCl acid and thus can be
removed provided it is accessible.
Calcium Sulphate (CaSO4.nH2O) has various forms depending on the
number of water of crystallisation molecules which it possesses. Some of the
most common forms are gypsum, hemihydrate and anhydrite. CaSO4 is
removed by its chemical conversion to CaCO3 which can then be removed
with acid.
Barium Sulphate BaSO4 is characterised by its very low solubility and it
chemical resistance to conventional mineral acids. Mechanical removal of the
scale is the primary treatment, although chemical treatments are being
developed.
Strontium Sulphate SrSO4 has only recently been recognised but because of
its inherent radioactivity poses not only a severe form of formation damage
but also extreme difficulties in its removal and disposal. Its occurrent in the
North Sea was reported as early as 1981 when a Radium 226 scale build up
within production tubing was reported. Since that time, an increasing number
of cases have been reported. The source of the radioactive material is from
one of two sources:
• By cumulative buildup of trace radioactive minerals as a result of
continued water injection into the reservoir
• By the leaching of radioactive salts from geological strata
particularly those with a high degree of shaliness or clay.
The deposition of radioactive scales normally occurs as coprecipitation with
barium and calcium sulphates. The physical form of the scale is such that the
strontium scale is encapsulated within the barium and calcium sulphate.
The complexity of scale solubility and precipitation is clearly evident from
Table 1. The relative solubilities of the various salts can be seen from Figure
32. It is clear that the BaSO4 has very limited solubility along with both CaCO3
and SrSO4. the solubility of the CaSO4 scales is greatly reduced with
increasing temperature.
Iron Compounds can also cause scale precipitation. However, the
concentration of iron compounds in both seawater and connate water is very
low and unlikely to be a source of sufficient material to create sever plugging.
A potential source of iron is from the rust and other iron scales which can form
on the inside of production tubing and be injected into the formation during
acid stimulation treatments or other injection operations. Iron compounds
must on occasion be accounted for in the design of an acid treatment by the
inclusion of a sequestering agent.
Crude oils are extremely complex mixtures of hydro-carbons which can vary
from a paraffinic or a straight chain alkane base to cyclic or asphaltic based
compounds. The production of hydrocarbons also requires a lowering in fluid
pressure as it moves from the reservoir through the production system. In
some cases particularly for very light oils and gases, the reduction in pressure
and associated expansion also gives rise to a reduction in temperature
(Joule Thompson cooling effect).
The two compounds which account for the majority of organic deposits are:
• Wax - paraffinic base
• Asphaltene - asphaltic base
Both these materials can range from the solid through semi-solid to the
viscous liquid phase since they cannot be exactly defined chemically but in
reality refer to a range of compounds with varying composition. These
materials can be deposited by one of two possible mechanisms.
Both were and asphaltene deposition can occur in the reservoir, wellbore or
production tubing. However, their formation in the reservoir is difficult to
identify. The most usual indications are:
pressure
K0 = Kro.K
where: K0 = the effective permeability to oil
The relative permeability – saturation relationship for a two phase mixture, say
oil-water, has the form shown in Figure 34. Clearly the greater the saturation
of a particular phase, i.e. the greater the fraction of the pore space it fills, the
less is the resistance to fluid flow through the rock system.
Thus for example, if a water based mud filtrate or completion fluid is lost to the
reservoir and invades the pore space it would reduce the oil saturation and
hence Kro. However, the oil saturation cannot be reduced below the
irreducible water saturation and would still retain a finite value for Kro and
hence still be mobile albeit at an extremely low rate. On production, the
invading fluid being more mobile would be produced back and oil from the
reservoir would replace it, thus increasing So and Kro. i.e. the production rate of
oil would gradually increase until the water saturation declined to the
irreducible water saturation.
The damage associated with the invasion of the pore space by a water based
fluid as described above is frequently referred to as:
• a water block
or
Frequently, the water based fluid lost to the formation, particularly if it is a mud
filtrate, may contain emulsifiers or surface active agents and these can affect
the wettability and cause more serious damage.
The problem of gas reservoirs is interesting in that in the natural state both
connate water and gas fill the pore space. If an oil mud, particularly water in
oil dispersion, is used, then the invading fluid may be oil giving rise to a 3
phase relative permeability effect and even greater temporary impairment of
productivity.
The principles of fluid flow in porous media dictate that a fluid which is in
contact with the rock surface will experience frictional drag and this reduces
its capacity to flow. The majority of reservoir rocks are originally water wet as
a result of their natural depositional environment. Carbonate reservoirs can be
oil wet or exhibit mixed wettability. It is evident from Figure 34 that if the oil
and water phases transfer such that the rock becomes oil wet then the curves
are also transferred, i.e. Kro for the water wet system becomes Krw for the oil
wetting system and vice versa. The impact of a change from water to oil wet
could reduce Kro several fold.
The wettability is controlled and stabilised by finely divided solids and other
materials which act as surface active agents. A change in wettability is
unlikely to occur naturally but may be influenced by events such as
asphaltene precipitation which may convert the rock from strongly wetting to
intermediate wettability. Changes in the physical conditions such as
temperature, pressure and pH may also influence wettability.
Damage created during casing and cementing operations is much less well
understood. However it is extremely likely that substantial damage may be
incurred.
• Check for any possible interaction between the cement filtrate and the
reservoir rock/ fluid system.
In the case of the previously perforated well, the casing has perforation which
are the sole entry point for fluid to flow from the reservoir. This therefore is a
crucial area of concern for damage.
The possibility of the fluid used for the well completion, interacting with
previous filtrates cannot be overlooked.
(3) Re-completion
• Avoid interactions with the reservoir rock/fluid and the prior invasion
fluids.
Normally for open hole or perforated completion after casing has been set, the
drilling fluid will be displaced out of the well and replaced by a completion fluid
which will hopefully provide some degree of formation protection, Table 2. A
large range of fluids are available, Table 3.
This requires the use of a solids free fluid to reduce the possibility of
particle plugging. However to obtain adequate control of liquid leak-off,
the fluid will normally be viscosified if the exposure time is extended.
The solids free approach must apply to the wellbore and surface facilities and
hence the “system” should be cleaned.
(1) Remove all mud from the well.
(2) Clean up the inside wall of the casing using scrapers.
(3) Clean all tanks and linework at surface which will hold the
completion fluid.
(4) Utilise filtration for all injected/circulated fluids.
The completion fluid would normally be viscosified to reduce the leak off rate
and hence invasion volume/radius. In addition to supplement fluid loss control,
it may be desirable to add bridging material to the fluid placed across the
productive zone. The bridging material will form an external filter cake. The
choice of material is normally:
• CaCO3 which is available in different sizes and is acid soluble.
• Oil soluble resins which are also available in different grades
and are produced back on oil flow.
• Saturated salt solution.
The specification of the solids is primarily defined by the bridging principles
discussed in Chapter 3. For a spotting fluid, the low fluid loss pill might
comprise 5-15 ppb of each of 2 or 3 grades of CaCO3. The use of these solids
in combination with a “solids free” fluid represents not a truly solids free
approach but a controlled solids fluid.
Frequently muds are still used for placement across formations during
well completion. Normally the same fluid as the drilling mud is used
thus offering economic advantages. Particularly in open hole
completions, the mum filter cake will prevent excessive leak off once it
is established. However the filter cake can be very permanent and not
easily removed, Figure 40.
The importance of fluid filtration to ensure controlled solids content was also
reported. A 1979 survey indicated that for one operator the productivities of
wells where the completion fluid was filtered to 10 µ m was 45% greater than
for wells where the fluid was only filtered to 25 µ m.
The second major concern is protection of clays in the formation. Most solids
free fluids are brines (see Table 3) and the presence of Na, K, Ca ions will
inhibit swelling. If NaCl or seawater is being used it is frequently desirable to
add some K ions by the addition of, for example, 2% KCl to the fluid. Most
brines will assist in clay protection. However this may not be true of other
fluids used for completions.
Open hole completions benefit from the following advantages over cased and
perforated completions:
They are however highly dependent for the productivity on avoiding damage
during the drilling phase.
• Minimise solids contact from the fluid except for bridging particles if
required.
• Check for possible interaction between the completion fluid and the
reservoir rock fluids. (Scaleformation, wettability alteration or emulsions
may be important).
Perforations are the key factor in cased well productivity. The productivity of a
perforated completion depends upon:
(2) The depth and permeability of the damage zone created during drilling
by subsequent fluid exposure to the perforations.
(7) Potential plugging of the perforation by solids from the fluid in the
wellbore.
• Mobilise fines.
• Disrupt the connate liquid film.
• Promote failure of grain to grain cementation.
The use of solids free fluids to protect perforated intervals is very important in
the following situations:
Contamination of a solids free completion zone can also occur due to:
McLeod also analysed the use of various types of fluids and pressure
conditions and verified the optimum approach as being the combination of
drawdown conditions and clear fluids (Table 4).
Perforations which will be exposed to well fluids for any extended period of
time should be protected by fluid loss control either by solid/granular additives
of CaCO3 or oil soluble resin and/or viscosifiers which should also be non
damaging e.g. HEC not guar.
When designing a fluid for bridging purposes using materials such as CaCO3,
it needs to be based on the following principles:
(1) Backflow
A perforation in a productive well are normally cleaned up to some
extent by the normal process of bringing the well onstream. Injection
wells, however, would not necessarily be cleaned up in the way. If the
perforations on an injection well have been protected by a fluid loss
control material either during completion or a workover, there are
benefits in backflowing the well prior to initiating injection. The question
arises as to what rate should be used to backflow perforations.
Normally a moderately high rate will be required to remove material
from the walls of perforations and the tunnel itself. In Figures 45 and
46, the effect of backflow rate on the clean up of material from the walls
of the perforation tunnel is evident. The flowrate used in Figure 45 was
five times that in Figure 46. A high magnification of Figures 45 and 46
are shown in Figures 47 and 48 respectively.
(5) Minimise fluid invasion prior to perforating and ensure that shot
penetration is selected to exceed the depth of the zone of drilling
damage.
To protect the formation during workovers the following steps may be of value.
(1) Use a minimal safe overbalance. The detrimental effects of high
differential overbalance pressures is evident from the S.E.M. pictures in
Figures 51 and 52 of tunnel walls plugged at 100 and 800 psi
respectively with a CaCO3 slurry.
(2) Use a clean preferably filtered fluid which is compatible with the
reservoir fluid.
(3) Use adequate fluid loss control either bridging solids or non-damaging
viscosifiers.
(4) Provide protection to clays in water sensitive formations use a brine or
a clay stabilising agent.
(5) Consider placing a high viscosity pill across the perforated interval
(100-200 cp viscosity, for example). Once this pill is in position avoid
disturbing it.
The principal causes of formation damage associated with oil and gas
production would be:
(3) Production of fines towards the wellbore due to excessive rates and
water cut.
Scales are formed by the mixing of incompatible waters and a change in the
physical conditions for the mixture i.e. changes in :
• Salt concentration
• Declining pressure
• Declining temperature
The deposition of a scale in the pore space can result in serious plugging
(Figure 53). The potential for scale precipitation must be assessed by
compatibility at reservoir and production conditions. Prediction based on
thermodynamics will also be of assistance. Given the complexity logistically of
scale dissolution and the associated costs, scale deposition should be
prevented. An effective inhibition treatment should be considered. In practice
it is difficult to perform inhibitor squeezes into the formation due to reservoir
heterogeneities. The possibility of damage generated by the inhibitor cannot
be overlooked particularly with respect to emulsion formation and alteration of
wettability.
Excessive drawdown (above that required for the (target) production rate) is to
be avoided.
• Bacterial plugging
Solids Plugging
(2) Ensure no rust, scale or mud in the wellbore during initial completion.
Bacterial plugging
Scale deposition
The presence of salts in the injected water is a major cause of scale forming
material. The scale will normally be produced not at the injection but at the
production well on water breakthrough.
Normally seawater or brine injected into the reservoir will possess sufficient
ions to control the extent of clay swelling. In severe cases or where fresh low
salinity water is being used it may be necessary to use a Hydroxy-aluminium
treatment around the injection wellbore. Coppel etc at discussed field results
with this chemical for clay stabilisation.
Gas injectors are also prone to solids plugging of the perforations. In fact due
to the high gas velocities in the tubing, hydraulic erosion can release rust and
scale from tubing. In view of the comments by Rike, these deposits can
severely plug and reduce perforation injectivity. Tubing for gas injections
should be thoroughly cleaned prior to use to remove all scale and rust.Another
aspect of potential importance is the possibility of injection gas contamination
from other sources, e.g. compressor lubricants.
Gravel packs in which the well is not under-reamed will reduce the natural
productivity of the well.
Damage during gravel packing can occur in a number of ways and can result
in:
The carrier fluid will transport the gravel into the wellbore and place it in
position between the screen and the formation or casing. The fluid therefore
can create damage due its leak off as follows:
(1) Interaction with the reservoir fluids or previous filtrates –
emulsions or scale deposits may result.
(4) Plugging by gel residue from the polymers in the carrier fluid.
Gravel sizing is normally based upon the mean sand size and a bridging size
factor.
With this ratio formation sand of the d50 size will bridge externally on the
gravel pack and not invade the pack.
Gulati and Maly investigated the effects of gravel pack invasion. Figure 56
illustrates effective gravel sizing with the formation sand being restricted on
the outside of the gravel pack i.e. no sand invades the pack. If too large a ratio
is used i.e. greater than 6, the pore throat sizes between the gravel particles is
large enough to allow gravel pack invasion by the sand. The result is a pack of
greatly reduced permeability as shown in Figure 57. The slight reduction in
pack permeability caused by using too small a gravel size is minimal
compared with the detrimental effects on permeability, of pack invasion. It is
important to ensure that no solids can invade the pack from various sources:
The effect of mud particles and invasion material entering the pack is shown
in Figure 58.
The use of acidisation in wells is faced with considerable difficulties and there
are numerous ways in which impairment can occur either due to the reaction
itself or the operational procedures.
4.4.8.1 Damage due to the acid reaction, acid additives or reaction by-
products
Despite the use of corrosion inhibitors there will always exist some
concentration of iron compounds in the fluid. The dissolved iron salts will
remain in solution provided the solution is acidic. However as the acid
becomes diluted and/or spends, the pH will rise and the iron compounds
particularly ferrous and ferric chloride will precipitate.
(e) Emulsions
Again due to the reduced interfacial tension, emulsions can be generated and
these may be stabilised by the fines released during the treatment.
The complex nature of chemical additives and the large variety of components
can lead to side reactions resulting in formation damage:
• Water blocking
• Formation and perforation plugging due to the presence of solids
(1) Pre-planning
(2) Treatment execution
Preplanning
(It is also worth evaluating the possible interaction of the acid with other fluids
which might occupy the pore space next to the wellbore e.g. gravel packing
fluids, completion fluids and drilling fluids.)
Treatment execution
Specific precautions depend upon the exact design of the treatment but the
following points apply.
The amount of residue generated from the fracturing fluid gel will
depend upon the gelling agent. If hydroxy ethyl cellulose H.E.C. is
used, the residue volume is reportedly small but if a guar gum is used it
will result in a residue of as much as 5%.
The amount of impairment by the gel reside can be substantial. The control of
clays may be enhanced by the addition of KCl or a clay stabiliser to the frac
fluid.
In line with all other processes involving fluid injection into the reservoir, the
following should be observed: