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:: WELL STIMULATION ::
WELL STIMULATION
 Well stimulation is the process by
which the productivity of a well is
increased. Productivity is measured
in terms of productivity index or JO
JO = q / P
 Productivity index (PI) is defined a
sth ration of flow of oil per unit draw
down (P = PR - PWf)
WELL STIMULATION:
OBJECTIVES
 Stimulation is a catcall term for a variety of
techniques designed to enhance well
performance in new wells, or restore
production in older wells. Stimulation of oil
and gas reservoirs, with a view to increasing
well productivity
 Initially applied in carbonate reservoirs, the
technique was extended to more complex
mineralogy
WELL STIMULATION: METHODS
 i. Hydraulic fracturing
 ii. Acidizing
 iii. Notroshooting
 iv. De-paraffination
WELL STIMULATION
HYDRAULIC FRACTURING
HYDRAULIC FRACURING:
Objectives
 The objectives of hydraulic fracturing for well
stimulation is to increase productivity of
producing zone by creating the highly
conductive path (compared to the reservoir
permeability) some distance away from the
well bore in to the formation
HYDRAULIC
FRACURING:Objectives
 A fracturing treatment consists in breaking
down a producing section hydraulically with a
sand carrying fluid, the sand being used to
prop the resulting fracture. Usually
conductivity is maintained by propping with
sand to hold the fracture face apart
HYDRAULIC
FRACURING:OBJECTIVES
i.To increase productivity by passing damage
zone.

 ii.To increase productivity in low permeability
formation by creating deep penetration fracture
(i,e, massive fracturing)
HYDRAULIC
FRACURING:MECHANISM
 i. Pressure parting in water injection
wells.
 ii. Lost circulation during drilling
operations.
 iii.The break down of formation during
squeeze cementing operations.
HYDRAULIC
FRACURING:APPLICATIONS
i. In a low permeability, homogenous rock,
fracturing is similar in effect to increasing the size
of the hole,
ii. Fracturing will eliminate formation damage due to
invasion of drilling mud, deposition of mineral
matter, or swelling of clays.
 iii.Fractures radiating from the well bore act as
gathering lines connecting permeable and
porous systems that are otherwise isolated form
the well by impermeable barriers.
INITIATION OF FRACTURES
 A hydraulic fracturing treatment is accomplished
by pumping a suitable fluid in to the formation at
a rate faster than the fluid can leak off in to the
rock. Fluid pressure or stress is built up sufficient
to overcome the earth compressive stress
holding the rock material together. The rock then
parts or fractures along the plane perpendicular
to the minimum compressive stress in the
formation stress in the formation matrix.
PARAMETERS FOR HYDRAULIC
FRACTURING
 For water pressure gradient is 0.426 psi/ft.
 For brine pressure gradient is 0.433 psi/ft.
 For over burden 1 psi/ft. 125 – 200 lbs/ft3
average 144 lbs / ft3.
 i. The fracture will be created in a plane, which is
perpendicular to minimum principal stress.
 ii. In deeper formation, tear is much easier than
lifting.
 iii.In shallower formation lifting is much easier
than tear apart.
INITIATION OF FRACTURES
 i. Pressure required to create a Horizontal
fracture
 Pf (h) = Z = 1.0 x D
 Where D is the depth in feet
 ii. Pressure required to create a vertical fracture
 Pf (v) = [ 2  / (1 -  ) ] Z + St
 Where  is Poisson’s ratio = lateral strain / axial
strain varies between 0.18 to 0.27 for the
average type of rocks.
 St = tensile stress.
OBSERVATION OF WELL
STIMULATION
 i. Success of the well stimulation
job can be found by evaluating
productivity index (PI) before and
after the job that is
 PI (after job) / PI (before job)
HYDRAULIC FRACTURING
 The well is
obstructed by silt,
sediments,
deposits.oil can’t flow
to the borehole
HYDRAULIC FRACTURING
 Water is
injected at a
very high
pressure
HYDRAULIC FRACTURING
 The obstructions
are forced out of
the oil producing
formation. Oil can
now flow freely!
USE OF PROPPANTS
 i. Fracture created in sandstone formation is
required to be propped by suitable propping
agents (or proppants).
 ii. Proppants are specially selected sands of
20 – 40 mesh size.
 iii. The proppants should be of uniform size
and spherical shape as possible.
PROPPING THE FRACTURS
 The objectives of the propping is to maintain
desired fracture conductivity economically.
Horizontal fracture sand used as a propping
agent tends to be crushed or embedded in
the fracture faces and recommended the use
of rounded crushed wall nut shells
PROPPING THE FRACTURS
 In present design sand concentration ranges
fro, 85 to 137.5 lb / ft2 of fracture are using
either 20 – 40 or 10 – 20 mesh sand.
However greater fracture capacity is required
the design are for 70 % 10 – 20 mesh sand
followed by 8 – 12 mesh angular sand are
recommended as propping agents,
WELL STIMULATION
ACIDIZING
WELL STIMULATION:
ACIDIZING
 Acid is used to remove damage
near the well bore in all type of the
wells. In carbonate formation acid
may be used to create linear flow
systems by acid fracturing. Acid
fracturing is not applicable in Sand
stone wells.
WELL STIMULATION:
ACIDIZING
 (1) Matrix acidizing is performed below
fracturing rate and pressure. Acid flow is
through the matrix with reactions being in
existing pores and natural fractures.
 (2) Fracture acidizing is performed above
fracturing rates and pressures. Etching of the
created fractures provides well stimulation,
not just damage removal
WELL STIMULATION:
MATRIX ACIDIZING
 It is primarily applied to remove skin damage
caused by drilling , completion, work over or well
killing fluids and by precipitation of deposits from
produced water .
 Due to extreme larger surface area contacted by
the acid in a matrix treatment, spending time is very
short. Therefore it is difficult to affect the formation
more than a few feet from the well bore. .
WELL STIMULATION:
MATRIX ACIDIZING
 Removal of severe plugging in sandstone,
limestone or dolomite can result in a very large
increase in well productivity.
 If there is no skin damage, a matrix treatment in
limestone or dolomite could stimulate natural
production no more than one and one - half
times.
 Matrix treatments tend to leave zone barriers
intact of pressure are maintained below fracture
pressure.
MATRIX ACIDIZING: USE OF ACID
 HCl (10 – 15%) is used for acid washing jobs in
which bottom hole is cleaned by acid reaction
with scale (CaCO3) etc.
 The deposition on the inside wall of tubing and
perforation plugging may be cleaned by acid
washing. A small amount of acid is provided by
to & fro circulation.
ACIDS USED IN MATRIX
ACIDIZING
 The acid is pumped at a pressure lower than
fractured pressure of the formation.
 The acid is intended to enter in to the matrices of
the rock.
 For carbonate (Limestone & Dolomite) formation
10 – 15% HCl is used.
 For sand stone formation, a combination of 12%
HCl + 3% HF called mud acid is used.
ACIDS USED IN MATRIX
ACIDIZING
 HCl provides reaction with carbonate present
in the matrices including with silica + clays.
Matrix acidizing is aimed at removal of
formation damage, thereby restore
productivity.
FRACTURE ACIDIZING
 Fracture acidizing or Acid Fracturing is an
alternative to hydraulic fracturing and propping
in carbonate reservoirs.
 In fracture acidizing, the reservoir is
hydraulically fractured and then the fracture
faces are etched with acid to provide linear
flow channels to the well bore.
FRACTURE ACIDIZING
 Fracture acidizing has no
application is sand stone wells.
Break down of a sand stone well
with acid at fracture pressure tends
to break down natural vertical
permeability barriers to adjacent
unwanted zones.
FRACURE ACIDIZING
SAND STONE ACIDIZING
 The primary reaction to acidizing sandstone
wells is to increase well permeability by
dissolving clays near the well bore.
 These clays may naturally occurring formation
clays or may have introduced from drilling/
completion or work over operations.
 HF can dissolve calcium carbonate, sand, clays,
shale and feldspars. However, the HF is used to
remove clay deposits form the rock matrix.
ACID USED IN FRACTURE
ACIDIZING
 In case of carbonate rocks 12-15% HCl is used for acid
fracturing job that is done at pressure more than fracture
pressure of the reservoir rock. For matrix acidizing, the
following procedure is required-
 First a pre-flush of about 10% HCl is pumped followed by
mud acid (12% HCl + 3% HF) volume that is called Pad
Volume. The pad volume is followed by a spocer flush or
after flush of 5% HCl.
HYDROCHLORIC ACID (HCl)
CaCO3 + 2HCl --------- CaCl2 + H2O + CO2
Lime stone+ AcidSoluble salt +Water +(gas evolved)
CaMg(CO3)2 + 4HCl -- CaCl2 +MgCl2+ 2H2O + 2CO2
Dolomite+Acid -- Soluble salts+ Water + (gas evolved)
HYDROCHLORIC ACID (HCl)
 i. Normally 15% HCl by weight is used in the field but the
concentration varies between 5% to 35%. The freezing
point of the 15% acid is –27deg F, less than –70degF for
20-29% and – 36 deg F for 35% acid. HCl will dissolve
limestone, dolomite and other carbonates.
 ii. A thousand gallons of 15% HCl will dissolve 1,840 lb or
01.5 cu.ft of zero porosity lime stone (CaCO3). This
reaction will produce 2,050 lbs of Calcium chloride
(CaCl2), 812 lb or 6,600 cu.ft. of Carbon dioxide (CO2)
gas at standard conditions of temperature and pressure.
In addition to the 7,600 lb of water injected as a carrier
fluid for acid, 333 lbs of water is also produced as the
part of the reaction.
HYDROCHLORIC ACID (HCl)
 III. In practice, after spending in lime stone, 1000
gal of 15% HCl becomes 1020 gal of 20%
solution of Calcium Chloride weighting 9.79 ppg.
 IV. A 1000 gal of 15% HCl will dissolve 1,7010
lb 0r 9.6 cu.ft. of Dolomite CaMg(CO3)2. The
spending of 1000 gal of 15% HCl in dolomite will
produce 1020 gal of mixture of Calcium Chloride
and 9% Magnesium Chloride weighing 9.7ppg.
HYDROFLUORIC ACID (HF):
 i. HF is used in oil, gas or service wells in normally 3%
HF combined with 12% HCl also called as Mud Acid. It is
employed exclusively used in Sandstone rock matrix
treatments to dissolve either natural clays or clays which
have migrated into the formation.
 ii.1000 gal of 4.2% HF acid will dissolve 700 lb of clay.
 iii.Fast reaction time and precipitation make HF acid
undesirable in carbonate containing sands having more
than 20% solubility in HCl. HF acid should never be used
in carbonate formation.
HYDROFLUORIC ACID (HF):
 SiO2 + 6HF --- H2 Si F6 + 2H2O
Sand Fluo-silicic Acid solution
 Al2 Si4 O10 (OH)2 + 36 HF--- 4 H2 Si F6
+ 12 H2O + 2H3Al F6
 Clay Fluo-Aluminic acid solution
HYDROFLUORIC ACID (HF):
 i.Reaction rate on sand and clay are
dependent on the ratio of the surface area of
the rock to volume of acid in the sandstone
matrix.
 The acid produced by the reaction of HF acid
on sand stone will react with NaCl or KCl in
the sand around the well bore to produce
insoluble precipitates.
HYDROFLUORIC ACID (HF):
 Fluo-silicic Acid
 H2 Si F6 + 2Na +  Na2Si F6 + 2 H+
 H2 Si F6 + 2K +  K2Si F6 + 2 H+
Precipitate
HYDROFLUORIC ACID (HF):
Fluo-Aluminic acid
 H2 Si F6 + 3Na + -- Na3 Al F6 + 3 H+
 H2 Si F6 + 3K + -- K3 Al F6 + 3 H+
i. The insoluble precipitate formed are Na2Si F6 ,
K2Si F6 , Na3 Al F6 ,
K3 Al F6. These fluorides are gelatinous type
materials and occupy a large volume of pore
space. They also adhere strongly to rock
surfaces. The results are very damaging to well
productivity.
HYDROFLUORIC ACID (HF):
 i. HCl can not dissolve clay or sand but can
dissolve carbonates present in sand stone
formation. HF acid reacts with lime stone and
precipitates calcium fluoride an insoluble
fine white powder.
 CaCO3 + 2HF  CaF2 + H2O +CO2
Precipitate
HYDROFLUORIC ACID (HF):
 To avoid precipitation in sand stone a pre-flush
of HCl is used to dissolve the lime stone and
prevent calcium ions from contacting HF acid.
 Sand stone formations have 20% more solubility
in HCl should normally be treated with HCl only.
ACETIC ACID (CH3COOH) :
 i. Acetic acid is a weak ionised & slow reacting
acid. A 1000 gal of 10% acetic acid will dissolve
about 1,110 lb of lime stone. The cost of
dissolving a given weight of lime stone is greater
than HCl.
 Acetic acid is very easy to inhibit against
corrosion and can usually be left in contact with
tubing or casing for days without danger of
serious corrosion. Therefore it generally used as
perforating fluid in lime stone wells
ACETIC ACID (CH3COOH) :
 i. Acetic acid is natural sequestering agent
against iron precipitation. It does not cause
embrittlement or stress cracking of high strength
steel.
 ii. It will not corrode aluminium.
 iii. It will not attack chorme plating up to 200
deg.F. Therefore it may be considered when
acidizing is done with an alloy pump in the hole.
FORMIC ACID (HCOOH):
 i. Formic acid is a weak ionised slow
reacting organic acid. It has similar
properties to acetic acid. However
formic acid is more difficult to inhibit
against corrosion at higher
temperatures and does not have
widespread acceptance.
ACID ADDITIVES
 i. Surfactants: To reduce surface / interfacial tension
to prevent emulsions to water wet formations.
Surface tension of 15% HCl is 72 Dynes/cm that can
be reduced up to 30 Dynes/cm by addition of the
additives.
 Suspending Agents: Most of the carbnate formations
contain fines which nay cause blockage in formation
pores or fractures if fines released by the acids are
allowed to settle and form bridges. Halliburton’s HC-
2 in concentration of about 5 Gal / 1000 gal of acid
mat be used to suspend fines for more than 24 hours
& possibly up to 7 days.
ACID ADDITIVES
 i. Sequestering Agents: to inhibit precipitation of iron
as hydrochloric acid spends. Acetic acid, Citric acid/
oxalic acid and lactic acid are common sequestering
agents.
 ii. Anti Sludge Agents: To prevent sludge formation
by keeping colloidal materials dispersed.
 iii. Corrosion Inhibitors: To slow down the rate of
corrosion. arsenic acid is more effective inhibitor
than organic inhibitor.
ACID ADDITIVES
 i. Alcohols: Methyl alcohol or IPA at the
concentration of 5% - 2% are used with acid to lower
the surface tension. The use of alcohol accelerates
the well clean up and improves clean up particularly
in dry wells.
 ii. Fluid Loss Controller: It may be required to
reduce acid leakage in fractures etc.
 iii. Diverting or Bridging Agents: These are used to
aloe relatively uniform acidizing of various porous
zones open to well bore.
OTHER IMPORTANT ADDITIVES:
 i. Corrosion inhibitors in small concentration of about
0.5% of acid volume is added in all three stages of
treatment to prevent corrosion Chromates, Di-chromates
of Potassium or organic inhibitors are used for the
purpose.
 ii. Surfactants 1% by volume of acid is used to reduce
interfacial tension between oil, water and acid so that any
formation of acid sludge is prevented.
 iii. Stabilizing agent 3% by volume of acid such as acetic
acid is used to stabilize formation clays and other fines.
OTHER IMPORTANT ADDITIVES:
 i.Sequestering agents (3% by volume) such As organic
acids (acetic acid/ oxalic acid/ citric acid) help to prevent
re-precipitation of salts of aluminium % iron.
 CaCO3 + 2HCl  CaCl2 + H2O + CO2
 Lime stone+Acid  Soluble salt +Water+(gas evolved)

OTHER IMPORTANT ADDITIVES:
Ca Mg (CO3)2 + 4HCl  CaCl2 + MgCl2 + 2H2O
+ 2CO2
Dolomite +Acid  Soluble salts+ Water+ (gas
evolved
CaCO3 + 2HF  CaF2 + H2O + CO2
Limestone+Acid Precipitate +Water+(gas
evolved)
OTHER IMPORTANT ADDITIVES:
 i. A Moderate rate of pre-flush is to prevent
reaction of carbonate with HF.
 ii. HF reacts with silica & clays and dissolved
them in to the HF solution.
 iii. Over flush pushes HCl + HF deeper in to the
formation to facilitate treatment in larger rock
volume.
 iv. Adequate mud acid is required for effective
treatment.
WELL STIMULATION
NITROSHOOTING
WELL STIMULATION:
NITRO SHOOTING
 Liquid explosive called nitro-glycerine was
pumped down hole & detonated. This results
in to high pressure gas which shatters rock
around bottom hole resulting in increased
permeability. The only problem is that the
whole process is uncontrolled. This method
has been discontinued.
DEPARAFFINATION
 Removal of wax or paraffin deposits from the
bore hole or the down hole equipment is
known as De- paraffination.
 Primary cause is cooling of oil due to
expansion of gas or oil, loss of heat etc.
 Paraffins can precipitate from crude on
changing the equilibrium conditions
WELL STIMULATION
DE-PARAFFINATION
DEPARAFFINATION
 Asphaltenes, fines and corrosion products
present in the system act as nucleating
materials and increase the binding force of
solid to get deposited.
 Deposition of asphaltenes on the formation
sand grains near the well bore that is oil wet
zone causes the plugging the permeable
zone and reduces the production
DEPARAFFINATION
 The most common methods of removing
paraffin deposits form wells are
i. Mechanical removal: use of scrappers and
cutters. Soluble plugs of microcrystalline wax
or insoluble plugs of hard rubber or sharp
edged plastic spheres have been found
useful in removing deposits.
DEPARAFFINATION
ii. Use of solvents: Chlorinated Hydrocarbon
such as Carbon Tetra Chloride, Carbon di-
sulphide are the various solvents to remove
the deposits.
iii. Use of dispersants: Water soluble
dispersants in the concentration of 2 – 10%
have been found effective
WELL STIMULATION
WITH SURFACTANTS
Well Stimulation using surfactants
Surfactants are chemicals that can be used to
improve the flow around the well bore. They
can
i. Raise or lower surface and interfacial tension.
ii. Make, break, weaken or strengthen an
emulsion.
iii. Change the wettability of reservoir rock, casing,
tubing and flow-lines.
iv. Disperse or floculate clays and other fines.
Well Stimulation using surfactants
 The real problem in emulsion removal from
sandstone formation with surfactant is the
near impossibility of getting the surfactant in
infinite contact with the emulsion droplets.
 Surfactant stimulation treatment form finger
or channel through a viscous emulsion.
 The majority of the untreated emulsion can
re-block the channels if not treated properly.
Well Stimulation using surfactants
 If the damage is oil wetting this can be
treated by injecting a strong water wetting
surfactant in to the formation.
 Cationics are very difficult to remove so the
use of cationics in sandstone should be
avoided.
Well Stimulation using surfactants
 Stimulation is usually carried out with a dilute
solution of surfactant 2 % - 3% in filtered oil or
filtrate salt water 2% KCl.
 Treatment size should be equal or greater the
size of fluid that has damaged the formation.
 An average treatment is 100 gal per foot (1.5 kL
per meter) of interval treated for the radius fo 3-5
ft. from the well bore with min.24 hours retention
time.
THANK YOU

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Well-Stimulation Well-Stimulation Well-Stimulation

  • 2. WELL STIMULATION  Well stimulation is the process by which the productivity of a well is increased. Productivity is measured in terms of productivity index or JO JO = q / P  Productivity index (PI) is defined a sth ration of flow of oil per unit draw down (P = PR - PWf)
  • 3. WELL STIMULATION: OBJECTIVES  Stimulation is a catcall term for a variety of techniques designed to enhance well performance in new wells, or restore production in older wells. Stimulation of oil and gas reservoirs, with a view to increasing well productivity  Initially applied in carbonate reservoirs, the technique was extended to more complex mineralogy
  • 4. WELL STIMULATION: METHODS  i. Hydraulic fracturing  ii. Acidizing  iii. Notroshooting  iv. De-paraffination
  • 6. HYDRAULIC FRACURING: Objectives  The objectives of hydraulic fracturing for well stimulation is to increase productivity of producing zone by creating the highly conductive path (compared to the reservoir permeability) some distance away from the well bore in to the formation
  • 7. HYDRAULIC FRACURING:Objectives  A fracturing treatment consists in breaking down a producing section hydraulically with a sand carrying fluid, the sand being used to prop the resulting fracture. Usually conductivity is maintained by propping with sand to hold the fracture face apart
  • 8. HYDRAULIC FRACURING:OBJECTIVES i.To increase productivity by passing damage zone.   ii.To increase productivity in low permeability formation by creating deep penetration fracture (i,e, massive fracturing)
  • 9. HYDRAULIC FRACURING:MECHANISM  i. Pressure parting in water injection wells.  ii. Lost circulation during drilling operations.  iii.The break down of formation during squeeze cementing operations.
  • 10. HYDRAULIC FRACURING:APPLICATIONS i. In a low permeability, homogenous rock, fracturing is similar in effect to increasing the size of the hole, ii. Fracturing will eliminate formation damage due to invasion of drilling mud, deposition of mineral matter, or swelling of clays.  iii.Fractures radiating from the well bore act as gathering lines connecting permeable and porous systems that are otherwise isolated form the well by impermeable barriers.
  • 11. INITIATION OF FRACTURES  A hydraulic fracturing treatment is accomplished by pumping a suitable fluid in to the formation at a rate faster than the fluid can leak off in to the rock. Fluid pressure or stress is built up sufficient to overcome the earth compressive stress holding the rock material together. The rock then parts or fractures along the plane perpendicular to the minimum compressive stress in the formation stress in the formation matrix.
  • 12. PARAMETERS FOR HYDRAULIC FRACTURING  For water pressure gradient is 0.426 psi/ft.  For brine pressure gradient is 0.433 psi/ft.  For over burden 1 psi/ft. 125 – 200 lbs/ft3 average 144 lbs / ft3.  i. The fracture will be created in a plane, which is perpendicular to minimum principal stress.  ii. In deeper formation, tear is much easier than lifting.  iii.In shallower formation lifting is much easier than tear apart.
  • 13. INITIATION OF FRACTURES  i. Pressure required to create a Horizontal fracture  Pf (h) = Z = 1.0 x D  Where D is the depth in feet  ii. Pressure required to create a vertical fracture  Pf (v) = [ 2  / (1 -  ) ] Z + St  Where  is Poisson’s ratio = lateral strain / axial strain varies between 0.18 to 0.27 for the average type of rocks.  St = tensile stress.
  • 14. OBSERVATION OF WELL STIMULATION  i. Success of the well stimulation job can be found by evaluating productivity index (PI) before and after the job that is  PI (after job) / PI (before job)
  • 15. HYDRAULIC FRACTURING  The well is obstructed by silt, sediments, deposits.oil can’t flow to the borehole
  • 16. HYDRAULIC FRACTURING  Water is injected at a very high pressure
  • 17. HYDRAULIC FRACTURING  The obstructions are forced out of the oil producing formation. Oil can now flow freely!
  • 18. USE OF PROPPANTS  i. Fracture created in sandstone formation is required to be propped by suitable propping agents (or proppants).  ii. Proppants are specially selected sands of 20 – 40 mesh size.  iii. The proppants should be of uniform size and spherical shape as possible.
  • 19. PROPPING THE FRACTURS  The objectives of the propping is to maintain desired fracture conductivity economically. Horizontal fracture sand used as a propping agent tends to be crushed or embedded in the fracture faces and recommended the use of rounded crushed wall nut shells
  • 20. PROPPING THE FRACTURS  In present design sand concentration ranges fro, 85 to 137.5 lb / ft2 of fracture are using either 20 – 40 or 10 – 20 mesh sand. However greater fracture capacity is required the design are for 70 % 10 – 20 mesh sand followed by 8 – 12 mesh angular sand are recommended as propping agents,
  • 22. WELL STIMULATION: ACIDIZING  Acid is used to remove damage near the well bore in all type of the wells. In carbonate formation acid may be used to create linear flow systems by acid fracturing. Acid fracturing is not applicable in Sand stone wells.
  • 23. WELL STIMULATION: ACIDIZING  (1) Matrix acidizing is performed below fracturing rate and pressure. Acid flow is through the matrix with reactions being in existing pores and natural fractures.  (2) Fracture acidizing is performed above fracturing rates and pressures. Etching of the created fractures provides well stimulation, not just damage removal
  • 24. WELL STIMULATION: MATRIX ACIDIZING  It is primarily applied to remove skin damage caused by drilling , completion, work over or well killing fluids and by precipitation of deposits from produced water .  Due to extreme larger surface area contacted by the acid in a matrix treatment, spending time is very short. Therefore it is difficult to affect the formation more than a few feet from the well bore. .
  • 25. WELL STIMULATION: MATRIX ACIDIZING  Removal of severe plugging in sandstone, limestone or dolomite can result in a very large increase in well productivity.  If there is no skin damage, a matrix treatment in limestone or dolomite could stimulate natural production no more than one and one - half times.  Matrix treatments tend to leave zone barriers intact of pressure are maintained below fracture pressure.
  • 26. MATRIX ACIDIZING: USE OF ACID  HCl (10 – 15%) is used for acid washing jobs in which bottom hole is cleaned by acid reaction with scale (CaCO3) etc.  The deposition on the inside wall of tubing and perforation plugging may be cleaned by acid washing. A small amount of acid is provided by to & fro circulation.
  • 27. ACIDS USED IN MATRIX ACIDIZING  The acid is pumped at a pressure lower than fractured pressure of the formation.  The acid is intended to enter in to the matrices of the rock.  For carbonate (Limestone & Dolomite) formation 10 – 15% HCl is used.  For sand stone formation, a combination of 12% HCl + 3% HF called mud acid is used.
  • 28. ACIDS USED IN MATRIX ACIDIZING  HCl provides reaction with carbonate present in the matrices including with silica + clays. Matrix acidizing is aimed at removal of formation damage, thereby restore productivity.
  • 29. FRACTURE ACIDIZING  Fracture acidizing or Acid Fracturing is an alternative to hydraulic fracturing and propping in carbonate reservoirs.  In fracture acidizing, the reservoir is hydraulically fractured and then the fracture faces are etched with acid to provide linear flow channels to the well bore.
  • 30. FRACTURE ACIDIZING  Fracture acidizing has no application is sand stone wells. Break down of a sand stone well with acid at fracture pressure tends to break down natural vertical permeability barriers to adjacent unwanted zones.
  • 32. SAND STONE ACIDIZING  The primary reaction to acidizing sandstone wells is to increase well permeability by dissolving clays near the well bore.  These clays may naturally occurring formation clays or may have introduced from drilling/ completion or work over operations.  HF can dissolve calcium carbonate, sand, clays, shale and feldspars. However, the HF is used to remove clay deposits form the rock matrix.
  • 33. ACID USED IN FRACTURE ACIDIZING  In case of carbonate rocks 12-15% HCl is used for acid fracturing job that is done at pressure more than fracture pressure of the reservoir rock. For matrix acidizing, the following procedure is required-  First a pre-flush of about 10% HCl is pumped followed by mud acid (12% HCl + 3% HF) volume that is called Pad Volume. The pad volume is followed by a spocer flush or after flush of 5% HCl.
  • 34. HYDROCHLORIC ACID (HCl) CaCO3 + 2HCl --------- CaCl2 + H2O + CO2 Lime stone+ AcidSoluble salt +Water +(gas evolved) CaMg(CO3)2 + 4HCl -- CaCl2 +MgCl2+ 2H2O + 2CO2 Dolomite+Acid -- Soluble salts+ Water + (gas evolved)
  • 35. HYDROCHLORIC ACID (HCl)  i. Normally 15% HCl by weight is used in the field but the concentration varies between 5% to 35%. The freezing point of the 15% acid is –27deg F, less than –70degF for 20-29% and – 36 deg F for 35% acid. HCl will dissolve limestone, dolomite and other carbonates.  ii. A thousand gallons of 15% HCl will dissolve 1,840 lb or 01.5 cu.ft of zero porosity lime stone (CaCO3). This reaction will produce 2,050 lbs of Calcium chloride (CaCl2), 812 lb or 6,600 cu.ft. of Carbon dioxide (CO2) gas at standard conditions of temperature and pressure. In addition to the 7,600 lb of water injected as a carrier fluid for acid, 333 lbs of water is also produced as the part of the reaction.
  • 36. HYDROCHLORIC ACID (HCl)  III. In practice, after spending in lime stone, 1000 gal of 15% HCl becomes 1020 gal of 20% solution of Calcium Chloride weighting 9.79 ppg.  IV. A 1000 gal of 15% HCl will dissolve 1,7010 lb 0r 9.6 cu.ft. of Dolomite CaMg(CO3)2. The spending of 1000 gal of 15% HCl in dolomite will produce 1020 gal of mixture of Calcium Chloride and 9% Magnesium Chloride weighing 9.7ppg.
  • 37. HYDROFLUORIC ACID (HF):  i. HF is used in oil, gas or service wells in normally 3% HF combined with 12% HCl also called as Mud Acid. It is employed exclusively used in Sandstone rock matrix treatments to dissolve either natural clays or clays which have migrated into the formation.  ii.1000 gal of 4.2% HF acid will dissolve 700 lb of clay.  iii.Fast reaction time and precipitation make HF acid undesirable in carbonate containing sands having more than 20% solubility in HCl. HF acid should never be used in carbonate formation.
  • 38. HYDROFLUORIC ACID (HF):  SiO2 + 6HF --- H2 Si F6 + 2H2O Sand Fluo-silicic Acid solution  Al2 Si4 O10 (OH)2 + 36 HF--- 4 H2 Si F6 + 12 H2O + 2H3Al F6  Clay Fluo-Aluminic acid solution
  • 39. HYDROFLUORIC ACID (HF):  i.Reaction rate on sand and clay are dependent on the ratio of the surface area of the rock to volume of acid in the sandstone matrix.  The acid produced by the reaction of HF acid on sand stone will react with NaCl or KCl in the sand around the well bore to produce insoluble precipitates.
  • 40. HYDROFLUORIC ACID (HF):  Fluo-silicic Acid  H2 Si F6 + 2Na +  Na2Si F6 + 2 H+  H2 Si F6 + 2K +  K2Si F6 + 2 H+ Precipitate
  • 41. HYDROFLUORIC ACID (HF): Fluo-Aluminic acid  H2 Si F6 + 3Na + -- Na3 Al F6 + 3 H+  H2 Si F6 + 3K + -- K3 Al F6 + 3 H+ i. The insoluble precipitate formed are Na2Si F6 , K2Si F6 , Na3 Al F6 , K3 Al F6. These fluorides are gelatinous type materials and occupy a large volume of pore space. They also adhere strongly to rock surfaces. The results are very damaging to well productivity.
  • 42. HYDROFLUORIC ACID (HF):  i. HCl can not dissolve clay or sand but can dissolve carbonates present in sand stone formation. HF acid reacts with lime stone and precipitates calcium fluoride an insoluble fine white powder.  CaCO3 + 2HF  CaF2 + H2O +CO2 Precipitate
  • 43. HYDROFLUORIC ACID (HF):  To avoid precipitation in sand stone a pre-flush of HCl is used to dissolve the lime stone and prevent calcium ions from contacting HF acid.  Sand stone formations have 20% more solubility in HCl should normally be treated with HCl only.
  • 44. ACETIC ACID (CH3COOH) :  i. Acetic acid is a weak ionised & slow reacting acid. A 1000 gal of 10% acetic acid will dissolve about 1,110 lb of lime stone. The cost of dissolving a given weight of lime stone is greater than HCl.  Acetic acid is very easy to inhibit against corrosion and can usually be left in contact with tubing or casing for days without danger of serious corrosion. Therefore it generally used as perforating fluid in lime stone wells
  • 45. ACETIC ACID (CH3COOH) :  i. Acetic acid is natural sequestering agent against iron precipitation. It does not cause embrittlement or stress cracking of high strength steel.  ii. It will not corrode aluminium.  iii. It will not attack chorme plating up to 200 deg.F. Therefore it may be considered when acidizing is done with an alloy pump in the hole.
  • 46. FORMIC ACID (HCOOH):  i. Formic acid is a weak ionised slow reacting organic acid. It has similar properties to acetic acid. However formic acid is more difficult to inhibit against corrosion at higher temperatures and does not have widespread acceptance.
  • 47. ACID ADDITIVES  i. Surfactants: To reduce surface / interfacial tension to prevent emulsions to water wet formations. Surface tension of 15% HCl is 72 Dynes/cm that can be reduced up to 30 Dynes/cm by addition of the additives.  Suspending Agents: Most of the carbnate formations contain fines which nay cause blockage in formation pores or fractures if fines released by the acids are allowed to settle and form bridges. Halliburton’s HC- 2 in concentration of about 5 Gal / 1000 gal of acid mat be used to suspend fines for more than 24 hours & possibly up to 7 days.
  • 48. ACID ADDITIVES  i. Sequestering Agents: to inhibit precipitation of iron as hydrochloric acid spends. Acetic acid, Citric acid/ oxalic acid and lactic acid are common sequestering agents.  ii. Anti Sludge Agents: To prevent sludge formation by keeping colloidal materials dispersed.  iii. Corrosion Inhibitors: To slow down the rate of corrosion. arsenic acid is more effective inhibitor than organic inhibitor.
  • 49. ACID ADDITIVES  i. Alcohols: Methyl alcohol or IPA at the concentration of 5% - 2% are used with acid to lower the surface tension. The use of alcohol accelerates the well clean up and improves clean up particularly in dry wells.  ii. Fluid Loss Controller: It may be required to reduce acid leakage in fractures etc.  iii. Diverting or Bridging Agents: These are used to aloe relatively uniform acidizing of various porous zones open to well bore.
  • 50. OTHER IMPORTANT ADDITIVES:  i. Corrosion inhibitors in small concentration of about 0.5% of acid volume is added in all three stages of treatment to prevent corrosion Chromates, Di-chromates of Potassium or organic inhibitors are used for the purpose.  ii. Surfactants 1% by volume of acid is used to reduce interfacial tension between oil, water and acid so that any formation of acid sludge is prevented.  iii. Stabilizing agent 3% by volume of acid such as acetic acid is used to stabilize formation clays and other fines.
  • 51. OTHER IMPORTANT ADDITIVES:  i.Sequestering agents (3% by volume) such As organic acids (acetic acid/ oxalic acid/ citric acid) help to prevent re-precipitation of salts of aluminium % iron.  CaCO3 + 2HCl  CaCl2 + H2O + CO2  Lime stone+Acid  Soluble salt +Water+(gas evolved) 
  • 52. OTHER IMPORTANT ADDITIVES: Ca Mg (CO3)2 + 4HCl  CaCl2 + MgCl2 + 2H2O + 2CO2 Dolomite +Acid  Soluble salts+ Water+ (gas evolved CaCO3 + 2HF  CaF2 + H2O + CO2 Limestone+Acid Precipitate +Water+(gas evolved)
  • 53. OTHER IMPORTANT ADDITIVES:  i. A Moderate rate of pre-flush is to prevent reaction of carbonate with HF.  ii. HF reacts with silica & clays and dissolved them in to the HF solution.  iii. Over flush pushes HCl + HF deeper in to the formation to facilitate treatment in larger rock volume.  iv. Adequate mud acid is required for effective treatment.
  • 55. WELL STIMULATION: NITRO SHOOTING  Liquid explosive called nitro-glycerine was pumped down hole & detonated. This results in to high pressure gas which shatters rock around bottom hole resulting in increased permeability. The only problem is that the whole process is uncontrolled. This method has been discontinued.
  • 56. DEPARAFFINATION  Removal of wax or paraffin deposits from the bore hole or the down hole equipment is known as De- paraffination.  Primary cause is cooling of oil due to expansion of gas or oil, loss of heat etc.  Paraffins can precipitate from crude on changing the equilibrium conditions
  • 58. DEPARAFFINATION  Asphaltenes, fines and corrosion products present in the system act as nucleating materials and increase the binding force of solid to get deposited.  Deposition of asphaltenes on the formation sand grains near the well bore that is oil wet zone causes the plugging the permeable zone and reduces the production
  • 59. DEPARAFFINATION  The most common methods of removing paraffin deposits form wells are i. Mechanical removal: use of scrappers and cutters. Soluble plugs of microcrystalline wax or insoluble plugs of hard rubber or sharp edged plastic spheres have been found useful in removing deposits.
  • 60. DEPARAFFINATION ii. Use of solvents: Chlorinated Hydrocarbon such as Carbon Tetra Chloride, Carbon di- sulphide are the various solvents to remove the deposits. iii. Use of dispersants: Water soluble dispersants in the concentration of 2 – 10% have been found effective
  • 62. Well Stimulation using surfactants Surfactants are chemicals that can be used to improve the flow around the well bore. They can i. Raise or lower surface and interfacial tension. ii. Make, break, weaken or strengthen an emulsion. iii. Change the wettability of reservoir rock, casing, tubing and flow-lines. iv. Disperse or floculate clays and other fines.
  • 63. Well Stimulation using surfactants  The real problem in emulsion removal from sandstone formation with surfactant is the near impossibility of getting the surfactant in infinite contact with the emulsion droplets.  Surfactant stimulation treatment form finger or channel through a viscous emulsion.  The majority of the untreated emulsion can re-block the channels if not treated properly.
  • 64. Well Stimulation using surfactants  If the damage is oil wetting this can be treated by injecting a strong water wetting surfactant in to the formation.  Cationics are very difficult to remove so the use of cationics in sandstone should be avoided.
  • 65. Well Stimulation using surfactants  Stimulation is usually carried out with a dilute solution of surfactant 2 % - 3% in filtered oil or filtrate salt water 2% KCl.  Treatment size should be equal or greater the size of fluid that has damaged the formation.  An average treatment is 100 gal per foot (1.5 kL per meter) of interval treated for the radius fo 3-5 ft. from the well bore with min.24 hours retention time.