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Table of contents
1.
PRESENTATION ..........................................................................................................................................5
1.1
GENERAL INTRODUCTION................................................................................................................5
1.2
THE CHALLENGES OF FLOW ASSURANCE ..................................................................................................7
1.3
DEVELOPING A FLOW ASSURANCE STRATEGY (FILE) ...............................................................................8
1.3.1
Data .................................................................................................................................................9
1.3.2
Risk assessment & Pre-sizing...........................................................................................................9
1.3.3
Management.....................................................................................................................................9
1.3.4
Sensitivity Studies...........................................................................................................................10
1.3.5
Project Studies ...............................................................................................................................10
1.3.6
Start-up and Production ................................................................................................................10
1.3.7
Flow Assurance file........................................................................................................................10
1.4
KEY PERSONNEL INVOLVED IN THE FLOW ASSURANCE GUIDE ................................................................12
PART 1 PHYSICO-CHEMICAL....................................................................................................................13
2.
HYDRATES .................................................................................................................................................15
2.1
THE ISSUES .............................................................................................................................................15
2.2
DATA REQUIRED .....................................................................................................................................18
2.3
METHODOLOGY ......................................................................................................................................19
2.3.1
Formation Prediction (thermodynamic range) ..............................................................................19
2.3.2
Evaluating the Risks of Plugging ...................................................................................................21
2.4
SOLUTIONS .............................................................................................................................................23
2.4.1
Prevention ......................................................................................................................................23
2.4.2
Hydrate solution and limitations for Dry Trees associated with wellhead platform .....................26
2.4.3
Monitoring .....................................................................................................................................27
2.4.4
Curative Methods...........................................................................................................................28
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3.
ORGANIC DEPOSITS................................................................................................................................32
3.1
WAXES .................................................................................................................................................32
3.1.1
The issues .......................................................................................................................................32
3.1.2
Data Required................................................................................................................................33
3.1.3
Methodology ..................................................................................................................................36
3.1.4
Solutions.........................................................................................................................................41
3.2
ASPHALTENES....................................................................................................................................44
3.2.1
The issues .......................................................................................................................................44
3.2.2
Data Required................................................................................................................................45
3.2.3
Methodology ..................................................................................................................................46
3.2.4
Solutions.........................................................................................................................................48
3.3
NAPHTENATES...................................................................................................................................49
3.3.1
The issues .......................................................................................................................................49
3.3.2
Data Required................................................................................................................................49
3.3.3
Methodology ..................................................................................................................................50
3.3.4
Solutions.........................................................................................................................................52
4.
SCALE ..........................................................................................................................................................55
4.1
4.2
4.3
4.4
5.
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7.
THERMAL MANAGEMENT....................................................................................................................96
7.1
THE ISSUES .........................................................................................................................................96
7.2
REQUIRED DATA ...............................................................................................................................97
7.3
METHODOLOGY ................................................................................................................................97
7.3.1
Under permanent flowing conditions.............................................................................................98
7.3.2
Under shutdown and restart conditions.........................................................................................99
7.4
SOLUTIONS .......................................................................................................................................101
7.4.1
Passive Insulation ........................................................................................................................102
7.4.2
Active Heating Systems ................................................................................................................105
7.4.3
Temperature monitoring ..............................................................................................................110
7.4.4
Hydrate prevention ......................................................................................................................111
8.
9.
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1. PRESENTATION
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For greater clarity and easy reading, the document is divided into two main parts:
PART 1 PHYSICO-CHEMICAL
Part I deals with physical and chemical aspects of flow problems, broken down into the four following
themes:
HYDRATES.
ORGANIC DEPOSITS (waxes, asphaltenes and naphtenates).
SCALE DEPOSITS (carbonates, sulphates and halite).
MISCELLANEOUS PROBLEMS (rheology, gels and emulsions).
PART 2 MULTIPHASE TRANSPORT
Part II covers MULTIPHASE TRANSPORT of fluids, discussed around four themes:
HYDRODYNAMICS and PRODUCTIVITY (friction losses, instabilities and artificial lift),
THERMAL MANAGEMENT
EROSION CORROSION
WELL METERING & MONITORING
We have tried to use the same presentation in our coverage of the different themes in both parts:
- an introduction to the ISSUES, aimed at defining the nature of the problem,
- an inventory of the DATA needed to conduct the study, in order to understand the
phenomena and identify the problems.
- a presentation of the general METHODOLOGY, explaining how the studies proceed and
what resources are implemented,
- and finally, a description of the SOLUTIONS that can be considered, to prevent or
remedy the different problems.
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Formation of hydrates,
Deposits,
Gelling point,
Productivity and Pressure drops
Flow Stability.
Deposition and associated plugging by both hydrates or waxes in lines are the largest risks currently
limiting oil extended reach subsea tieback (in excess of 25-30 Km). Other potential deposits such as
scale or asphaltenes are also to be addressed but generally at a lower priority.
Associated with the production of fluids, cooling and reduction in pressure from the reservoir to the
host facility are inescapable. This may induce phase changes including the separation of gas and
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liquid, the phase slippage or the formation of solids. Multiphase transport of fluids presents number of
challenges to be managed in order to assure flow and ensure the integrity of the production system.
These issues tend to be fluid and system specific.
Flow Assurance studies strategy
Flow Assurance studies consider hydrodynamic and thermal behaviour, together with the
thermodynamic, chemical and physical characteristics of the effluents. They therefore entail thorough
analysis of the fluid stream, from the reservoir to the surface installations.
Their results are used to identify potential problems to be tackled as early as possible in the
development design phase, and to propose solutions in line with the project technical and cost
objectives, such as:
-
Quantifying and managing production-related risks to avoid costly interventions on wells and
subsea equipment
This approach is initiated in the pre-project phase and continues well beyond the construction and
installation phases throughout the duration of the field's operation.
The preferred current strategy available for dealing with hydrates and waxes is still to insulate and
possibly heat the fluids to prevent them from cooling into the solids formation region during normal
operation and for limited shut-in times.
Remote subsea production in deepwater rely on a combination of prevention and remediation solutions
to guarantee uninterrupted production, flow assurance strategies involve an association of equipment
design & selection, operational methodologies and chemical treatments.
Flow Assurance studies focus on developing prediction tools as well as identifying and developing
prevention and curative solutions, in order to better quantify the risks of plugging a production system
and in qualifying or improving the performance of prevention, inhibition and remediation technologies.
Flow Assurance mission is to identify, promote and develop new technologies that insure the
uninterrupted flow of production from subsea reservoirs to process facilities at minimum capital and
operating costs without undue risks to environment, personnel and installation.
For the current near term (3-5 years) the objective is to optimise current design practices and
operation, to improve prediction software by analysing acquired data during operation and in parallel
identify, evaluate and improve prevention and remediation technologies.
Long term strategy has to provide technologies to allow for the minimal CAPEX/OPEX production
system as single un-insulated flowline. Associated with this minimal design the ability to quickly and
safely remediate any potential restriction is crucial (low cost intervention system).
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As a result flow assurance must be integrated into the overall subsea systems engineering effort, to
integrate flow assurance with system/equipment selection, elaboration of operational guidelines and
development of blockage remediation strategies.
1.3.1 Data
The first stage involves listing and assembling the data essential for the different studies. Obtaining
reliable data is one of the keys to evaluation of the risks associated with produced fluids,
reservoir behaviour, production profile, but also with the adjacent functions like water and gas injection.
1.3.3 Management
Using the different operating modes (normal and downgraded), Management studies then seek
solutions regarding:
Flow Management for steady state and transient flow, dealing with,
unstable conditions (hydrodynamics and severe slugging),
shut-in and restart conditions,
artificial lift based on the well eruptivity limit,
erosion-corrosion,
well metering.
Deposit Management. Mineral and organic deposits are quantified for the different
operating modes. Solutions for prevention, and possible curative means are described in
detail.
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Verification of the capacity of wells, pipes, subsea and surface equipment to handle prevention
and remediation,
Basic and detailed engineering of the production system (subsea and surface) in connection with
flow assurance, such as selection of chemicals, chemicals injection system, sampling points
Throughout the project phases, each Project Technical Review (PTR) includes a Flow Assurance
evaluation.
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Exploration
Pre-Project
Project
Start-up
Production
Exploitation
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Risk assessment
Operating Logic
Sensitivity studies
Monitoring issues
Detailed Engineering
Sampling
Thermal behaviour
Hydrodynamic Behaviour
Monitoring
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Presentation
Name
Entity
HYDRATES
JL PEYTAVY
TDO/EXP
ORGANIC DEPOSITS
Waxes, Asphaltenes, Naphtenates
Asphaltenes only
Naphtenates only
JL VOLLE
C. SCHRANZ
H. ZHOU
C. HURTEVENT
TDO/EXP
SCR/ED
TDO/EXP
TDO/EXP
JL VOLLE
TDO/EXP
C. HURTEVENT
TDO/EXP
D. LARREY
P. BRANJONNEAU
SCR/ED
TDO/EXP
D. LARREY
SCR/ED
P. BRANJONNEAU
Ex. TDO/EXP
EROSION CORROSION
M. BONIS
TDO/TEC
L. THOMAS
Ex. SCR/RD/UGF
MISCELLANEOUS PROBLEMS
Rheology, Gels, Emulsion
SCALE DEPOSITS
Carbonates, Sulphates, halite
HYDRODYNAMICS and PRODUCTIVITY
Pressure losses, Instabilities, Artificial lift
THERMAL MANAGEMENT
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Part 1 Physico-chemical
HYDRATES.
ORGANIC DEPOSITS
vWaxes
vAsphaltenes
vNaphtenates
SCALE DEPOSITS
vCarbonates
vSulphates
vSalts
MISCELLANEOUS PROBLEMS
vRheology
vEmulsions
vSeparation
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Hydrates
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2. HYDRATES
Fig 5.1 A
General issue: The major difficulty in controlling the risk represented by hydrate formation stems
from the fact that only the thermodynamic conditions governing their existence can be satisfactorily
predicted. We are extremely short of knowledge on the kinetics of their formation and growth,
especially in the presence of oil, leading to a plug forming.
The first practical consequence is that, when a prevention system fails, we can no longer control
the formation of hydrates and are thus reduced to counting on huge injections of thermodynamic
inhibitor (methanol or glycol) and plenty of good luck!
While the formation of hydrates systematically entails a risk of plugging, this does not necessarily
mean that plugging will actually occur. The presence of geometrical or thermal irregularities is in
this respect fairly critical.
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Part 1 Physico-chemical
Nor is there any direct relation between the quantity of hydrates formed and the plugging speed. In
a flowline several inches wide, the plugging process may be fairly slow (taking several hours and
even several days). A substantial amount of material is needed for a plug to form.
On the other hand, a relatively small quantity of hydrate may be enough to instantly plug a valve
(e.g. during re-opening of an SCSSV, if a gas pocket, formed upstream during shutdown, comes
into contact with water segregated downstream).
Finally, as far as prevention methods are concerned, the economic issue hinges above all on the
produced water flow rate. Thus, we can clearly see (figure below) that the continuous injection of
chemicals beyond a certain rate of water flow will become crippling. This water flow limit has to be
defined on a case-by-case basis, but, a priori, we can consider:
gas fields (with a low liquid content) where continuous injection of chemicals will be
economically viable, and
oil fields, where the water flow rate to be inhibited will, sooner or later, become totally
unacceptable; especially when water injection is used to ensure reservoir pressure
maintenance.
5
4.5
4
Methanol
-20C subcooling
3.5
Methanol
3
-10C subcooling
2.5
2
1.5
1
0.5
0
0
10
11
watercut (%)
Fig 2.1 B
12
13
14
15
16
17
18
19
20
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Rapid or even instantaneous plugging of flowlines, leading to significant production losses due to
the difficulties of intervention.
Rupture of the line subsequent to a projectile effect when the plug dissociates with under-balanced
pressure (velocity of 18 to 80 m/s).
Bursting of the flowline with local overpressures when evacuation of the gas during dissociation
(180 v of gas / v hydrates) is not possible.
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Part 1 Physico-chemical
In Deep offshore contexts
For oil fields, despite preventive measures based on thermal insulation, the major risk that subsists lies
in the re-start phase after a long unscheduled shutdown. At shutdown, the risk of a plug forming is near
to zero. On re-start, a massive, even explosive formation of hydrates may occur, leading to extremely
rapid plugging of flowlines.
M Remediation means are limited and time consuming in deepwater context. After plugging the line
with an hydrate plug that has cooled down to ambient (4C), dissociation time can extend into several
months if the pressure cannot be reduced to very low value (< 4 bar). Graph here after shows the
predicted plug dissociation times for an oil system.
500
400
300
200
100
0
0
50
100
150
200
250
the molar composition of the effluents, at least C1, C2, C3, iC4, nC4, N2, CO2 and H2S,
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Part 1 Physico-chemical
the pressure and temperature profiles of the evacuation stream (wells, flowlines and risers) from
OLGA type modelling, under steady and transient phases.
The maximum sub-cooling expected along the lines will be deduced from these data (hydrate
curve and operating range).
For oil fields, the feasibility of hydrate transportation in slurry needs to be assessed on a specific
pilot rig.
2.3 Methodology
Pressure Bar
200
180
160
140
120
100
80
60
40
20
0
Hydrate formation
No Hydrate
0 g/l NaCl
60 g/l NaCl
0
12
16
20
24
Temperature C
It is important to remember that the problem has to be dealt with in the same way, whatever the state
of the effluent and the phases present, and regardless of whether the phases are "free", dissolved,
liquid, or emulsified.
There are several software applications capable of calculating the P, T, and hydrate formation region,
among them:
Equiphase (integrated in Pro II),
CSMHYD (developed by D. Sloan's team at the Colorado School of Mines),
Aqua*sim (integrated in SHG),
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Part 1 Physico-chemical
3 50
3 25
3 00
2 75
Pressure (bara)
2 50
2 25
2 00
1 75
1 50
1 25
S h allo w
S h allo w
S h allo w
S h allo w
1 00
75
50
A q ua sim
E q uiph as e
C S M H YD
F hyd
25
0
0
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
T e m pe ra tu re (C )
These software applications are calibrated against experimental measurements and generally deliver
similar results.
However, we have observed some differences (see curves above), and it is best to systematically
compare the calculation results of at least 2 of them.
Where a substantial interval persists (> 2 - 3C), it is advisable to perform experimental PVT cell
measurements to define the formation range.
80
Pressure (bars)
Remark:
The intersection Pi, Ti of the hydrate
curve (see curve here aside) and the
bubble curve (quadruple point) must be
determined carefully when located in the
operating range conditions.
70
hydrate curve
60
50
Quadruple point
40
30
hc bubble curve
20
10
Pi
0
0
12
Temperature (C)
Ti
16
20
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Asphaltenic crude oils. The presence of resins and asphaltenes gives them the interfacial
properties to stabilise an emulsion of water in oil. The slurry is thus stabilised when the droplets of
water turn into hydrates. Examples of asphaltenic crudes include FROY, TROLL and ALBACORA,
which can transport a hydrate slurry with up to 30% water.
Acidic crude oils. The combined presence of naphtenic acids in the oil and sodium and/or calcium
salts in the water, under certain pH conditions, generates naphtenates at the oil/water interface.
These components are well known for their surfactant properties and capacity to stabilise the
slurry. Among acidic crudes, we could mention that during loop test with HEIDRUN oil we didnt
plug the test line up to 30% water.
To conclude, for oil fields, in addition to the thermodynamic study, an experimental evaluation of the
transportation potential needs to be performed, either on the CSTJF pilot rig or on the IFP loop in
Solaize (see photo here after).
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2.4 Solutions
2.4.1 Prevention
Various means of prevention can be envisaged. They are classified into four categories:
Keeping the temperature of produced fluids above the hydrate formation threshold. The effluent
flows from the wellhead at a temperature higher than that conducive to hydrate formation. To
maintain this condition in subsea pipelines, with an ambient temperature at 4C, we need to limit
heat exchanges. That means insulation and sometimes heating of the lines (for more details see
7 Thermal Management).
During a long shutdown, the temperature is maintained above the hydrate formation threshold for
a limited period (passive insulation) and even permanently (heating device).
But insulation performances have to be carefully checked before implementation, a number of
previous experiences having shown them to be poorer than expected due to thermal losses,
particularly on singular points with a different thermal signature (manifold, valves, connectors,
etc.).
Passive thermal insulation alone is not sufficient for prolonged shutdowns. To avoid plugs, which
can take a long time and be costly or even impossible to dissociate (several days to several
months), we have to consider additional means:
1.
Replacing the effluents by dead oil. Start-up then proceeds by circulating (loop
arrangement) the stock-tank oil to warm up the lines and, further on, by opening the wells
while massive shots of methanol are injected. Any parts of the system not located on the
production circulating loop, must be flushed with methanol.
2.
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Part 1 Physico-chemical
3.
Maintaining the fluid temperature outside the hydrate region by permanent heating
activated during shutdown (case A).
T e m p e r a tu r e
F lo w in g T e m p .
P R O D U C T IO N
S t a r t e le c tr ic H e a tin g
C r itic a l te m p .
2 0 C / 7 6 F
H y d r a te R e g io n
S e a te m p .
4 C / 4 0 F
T IM E
D e fa u lt
SHUTDO W N
Case A
Maintaining the temperature outside the hydrate region by electrical heating of lines
4.
After a total black-out, if all power generation is lost, the fluid will cool down to ambient
temperature, and then when power generation will be available re-heating the effluents to
quit the hydrate region before any start-up of producers(case B).
Temperature
Fluids
Stabilization
Flowing Temp.
Re-Start Production
Well opening
PRODUCTION
Stop Heating
Critical temp.
20C
Start Heating
Hydrate Region
4C
Required duration
TIME
Default
SHUTDOWN
Case B
Heating fluids before start-up of wells
These last two active solutions can only be considered for lines equipped with an heating system
(electrical, hot fluid, etc.).
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Continuous injection of chemicals is nowadays only economically viable for fields with low water flow
rates (a few hundreds of barrels/day) i.e. gas fields. When the water rate to be inhibited represents
several thousands of barrels/day and the sub-cooling to be overcome is around 15-20C, the
continuous use of any sort of chemical inhibitor becomes unrealistic.
There are 3 families of chemical inhibitors, with different modes of action at different stages of
industrial development:
v 1- Thermodynamic inhibitors: like (non-recycled) methanol and (in principle, regenerated)
glycols. These are antifreeze type products. They act by displacing the hydrate formation region.
This is therefore by far the most reliable method and the one most often used. The quantity of
methanol and glycol inhibitor that must be present in the water can be predicted by the models
mentioned above and will depend directly on the desired drop in temperature with respect to
hydrate formation.
Remarks:
- the total quantity of methanol to be injected must take into account losses in the gas and oil
phases,
- the presence of salts in the water to be inhibited, although favourable from a
thermodynamic point of view, can lead to 2 types of limitations:
when methanol is used, the solubility of the salts will be considerably reduced.
For example, the solubility of NaCl dwindles from 270 to 150 g/l when the
methanol content increases from 0 to 30% weight. The risk of precipitation of
salts can thus increase significantly (salt bridges), thereby impairing inhibition
of hydrate formation,
the fouling, or even corrosion, of boilers with the presence of salts often makes
the re-generation of glycol almost impossible.
v 2- Low Dosage Hydrate Inhibitors (LDHI): These new additives are not currently used yet in
deepwater conditions (subcooling > 15C or BSW > 50%). Although the active material is relatively
expensive as compared with methanol, their low dosage may result in significant cost cuts (Fig 2.1
B).
Remark: before deciding to use these additives, experimental work is always needed to optimise
the active material formulation and quantify the injection rate.
The LDHI additives are of 2 types:
kinetic Inhibitors (KHI), hydrosoluble polymers, injected at low dosage (generally
0.5% weight of active material versus water content). They retard the crystal growth
and prevent hydrate formation for the time needed to transport effluents under
hydrate region conditions. Their performance is limited, at least for the time being,
to relatively mild cases of sub-cooling (< 10C).
An inhibitor of this type, developed by BP/TROS, was tested industrially in 1997 on
a 12 pipeline between Pont dAs and Lacq, in mild conditions (sub-cooling 6C).
The results were positive as far as the additive's capability to inhibit hydrate
formation was concerned. However, problems of emulsion and foaming were
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observed on the downstream facilities. Before any use, we need to carefully assess
this issue.
Despite many other tests on fields, these inhibitors are still seldom used in
continuous injection. BP has been using them since 1997 on a North Sea line
covering 70 km from the HYDE field to the Easington terminal to replace the
methanol planned in the initial design. On the MUNGO field (ETAP field run by BP),
a kinetic inhibitor is injected to prevent hydrate formation when there are long
scheduled shutdowns. To date, performance is not fully satisfactory since the subcooling is around 10C. An instance of plugging was reported in 2001.
Anti-Agglomerants (AA) or dispersant additives, hydrocarbon soluble polymers,
also injected in low dosage (generally 1% weight of active material versus water
content). These do not prevent the formation of hydrate crystals, but limit their size
and keep them in suspension in the liquid phase as slurry. These additives are still
at the development stage. Their scope is limited, at least for the time being, to
moderate BSW (< 30 to 40%). The presence of a liquid hydrocarbon phase is
necessary i.e. these chemicals do not control hydrtates in a gas-water system.
They may become economically applicable for many cases once the subsea water
separation technique is available.
An additive of this type (Emulfip 102 B), developed by TFE and IFP, was recently
tested on the CANADON Alfa field in Argentina. The relative failure of the test can
be attributed to extremely severe conditions (laminar flow, temperature sometimes
lower than 0C and sub-cooling of around 20C).
Other tests need to be conducted before concluding as to the feasibility of this
prevention process.
An AA additive ( RE 4394 HIW from Baker Hughes) is presently under test on Shell
Popeye field, in a subsea flow line which is operated at 12 C subcooling.
Shell is preparing an other test with an AA chemical Armoclear 2550 on a satellite
of SEAN ( North Sea) This will be the first industrial application of AA.
3- The natural oil surfactant properties: This way of controlling hydrates obviously needs to be
validated in the field. This is the goal of current JIPs.
But a priori, we can say that it has one sure advantage in that it is free! Its application, as for AA
additives, is limited by the BSW, but here too, the development of subsea water separation could
render this method viable in a very large number of cases without incurring extra costs.
2.4.2 Hydrate solution and limitations for Dry Trees associated with wellhead platform
The main concern for dry tree risers in deepwater is the hydrate formation leading to plug the
production tubing during shutdown or associated restart phase.
The classic design for dry tree riser (isolation by nitrogen in the inner annulus) can provide a very short
cooldown (delay) before the fluid enters in hydrate domain. This cooldown time depends upon the
pressure of the nitrogen in the annulus (2 hours and lower).
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In mid water depth, operations of WHP do not lead to hydrate plugging controversially in deepwater,
low seabed temperature and high shut in pressures can result to get severe incursion into the hydrate
region (on the order of 20 C in some cases).
As the SCSSV is located as deep as to operate out of hydrate domain, depending on water cut and
GOR, depressurisation of riser after closing SCSSV may not reduce significantly the pressure at the
mud line out of hydrate formation.
On the other hand, remediation of hydrate plug can be handled easily with coiled tubing technique.
But in the case of multiple wells (more than 10), using coiled tubing to restart after shutdown is not
realistic due to economic impact.
Riser insulation and or active heating techniques have to be improved to give sufficient cooldown for
preventive actions.
Production restart with dry trees at high water cuts is also a main issue. During the restart period
MeOH injection will prevent hydrate formation.
This thermodynamic inhibition injection is maintained until a sufficient temperature is reached to give
required cool down in the case of new shutdown. The design of completion limits the inhibitor injection
line diameter an subsequently methanol or LDHI injection rate to less than 10 gal/mn. (Matterhorn < 5
gal/mn w/ 9/16 injection line).
At high water cuts, this limitation in injection will impact the production rate at which the well can be
restarted.
Lower flowrates during restart phase result in longer warm-up times and consequently in large volumes
of methanol.
2.4.3 Monitoring
As mentioned above, a distinction needs to be drawn between hydrate formation and plugging by
hydrates. But detection of the presence of hydrate crystals in effluents should provide warning.
At present, there is no one universal way of detecting the formation of a hydrate plug. The following
four observations should, however, act as a warning and so trigger or increase the injection of inhibitor
as a preventive measure:
-
Pressure measurement (pressure drops) and temperature measurement to evaluate the operating
range as opposed to the hydrate formation region. Temperature measurement throughout the
liquid stream by a non-intrusive optical fibre (DTS Distributed Temperature System) provides
monitoring of fluid temperature all along the lines (see for more details in 7.4.3).
reduction in the water flow at the separator on the receiving installations (gas applications),
gradual increase in pressure drops, especially if punctuated by sudden drops (sign that a plug is
being formed and partly tearing free from time to time).
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1- Injection of thermodynamic inhibitors. This method is generally a long and painstaking matter
but is reliable provided the inhibitor actually manages to make contact with the plug (with, as a
corollary, the problem of multiple plugs!). It therefore can only be used if the plug is perfectly located
and the inhibitor can migrate to reach it.
Remark: due to its density of 800 kg/m3, methanol may not traverse an oil layer by the effect of
gravity to reach the sedimented water part.
2- Depressurisation. This should be performed, whenever possible, on both sides of the plug. It is
the most commonly used method, as it is simple and effective and you do not need to know the
precise plug location. However, if you only depressurise on one side, there is a risk of making a
plug behave like a cannonball, likely to damage the pipeline system.
A model on radial dissociation has just been developed by the Colorado School of Mines (D. Sloan)
within the framework of the DEEPSTAR JIP. This is the first model of its kind and is claimed to be
capable of predicting the time needed for radial dissociation of the hydrate plug by depressurisation.
One limitation to this method emerges in Deep Offshore oil production. The residual static pressure
after depressurisation can be higher than the minimum pressure required to quit the Hydrates
region. Furthermore, in a thermally insulated pipe excessively long dissociation times are to be
expected because of the endothermic nature of hydrate dissociation.
3- Heating: This method is not recommended when it is impossible to evaluate the length of the
plug (which is often the case in subsea pipes), heating must be banned as a precaution. Indeed,
if evacuation of the gas released cannot be ensured due to the plug sealing effect, the pressure
may increase exponentially with temperature (heating mode) and ultimately cause rupture of the
pipeline. Conversely, if the pipeline is within the hydrate region during prolonged shutdown but no
plug has formed, the heating approach can be recommended to get effluents out of the hydrate
region BEFORE re-starting production (see 7.4.2 active heated systems).
However, recent study performed by SHELL provided a detailed analysis on hydrate dissociation
by electrical heating demonstrating that it is technically feasible, operationally safe and efficient
means for plug remediation. During dissociation pressure increases is relatively modest compared
to the pipe burst pressure and a very small gap (pipe wall and hydrate plug) is required to discharge
a very small mass of gas at large pressure difference. Hydrate dissociation process which is
endothermic, will quickly consume heat transferred from the pipe wall. Pipe wall temperatures do
not approach the value required to support pressures near the pipe burst limit. Based on the
conclusion of this study Electrical Heating will be used (installation in 2003) for Nakika field (WD:
1900m) for hydrate remediation on the different flowlines (10 x 16 PIP length 2 to 12.8 Km).
4- Mechanical, by drilling or jetting effect. This method can be associated with the injection of
thermodynamic inhibitors to combine both (mechanical and chemical) effects.
Remediating for oil dominated system by the use of intrusive system as an Extended Reach
Coiled Tubing Technique going gradually along the riser and the flowline up into contact with the
hydrate plug(s) to dissociate them by circulating tank battery oil and/or methanol.
This method is now limited by the size of the coiled tubing available on the market, its weight,
tensile limits and mechanical stability, and its ability to slide into bends.
Usual diameters range from OD up to 3 OD.
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Classic drums available have lengths of between 450 and 600m of steel tubing, the limit being due
to the maximum diameter and weight.
One limit to the range of action for CT stems from the buckling effect, which can cause spiral
winding on the internal wall of the pipe after too high a thrust. The buckling effect will depend on the
ratio between the internal diameter of the pipe and the outer diameter of the Coiled Tubing.
To use this technique, you need to take into account geometrical specifications in terms of bending
radius and change in direction during the design phase.
Recommended curve radii range from around 6 to 18 m.
Recent works conducted over 1997-1998 within the framework of the DEEPSTAR JIP highlighted
the advantage of combining a crawler and hydraulics (Jet and piston effect developed by RADOIL
providing 15T traction for 70 bars P at the CT head to pull the coiled tubing rather than push it.
A skate system developed by AMBAR ensures partial contact between the CT and the pipe wall to
limit friction.
After tests combining the crawler and skates, the maximum range for this technique has been
extended to about 8 10 kilometres.
Other crawlers are also available from WELLTEC, ASTEC and DACON.
Another means of improvement is to use composite coiled tubing. Here, the main advantages are
reduced weight (1/4 to 1/3 the weight of steel CT) and mechanical resistance to fatigue. The FIBER
SPAR Company offers this type of equipment (OD from to 6).
Typical functional requirements for hydrate plug removal systems (HPRS):
1. Deploy in the production riser a means of circulating a chemical inhibitor (methanol)
associated with a jetting effect. The hydrate plug has to be destroyed and dissociated by
overbalance in order to avoid cannonball effect.
2. Deploy in the production riser a depressurising means (gas or nitrogen lift) to re-start
production without any risk pressure & temperature) of a new hydrate plug.
3. Run-in and out without causing any damage to production equipment.
4. All parts of the HPRS have to be fishable in order to retrieve any loosen part.
A generic study on Hydrate Removal in flowline & riser has been generated by UGF R&D
project and is performed by Halliburton Deepwater, conclusions should be available beginning
2002. The aim of this study is first to establish the feasibility of hydrate removal in deepwater oil
production lines (Risers & Flowlines) and then define the general specification to incorporate in the
development design phase to facilitate hydrate removal interventions. Also the study will identify today
limitation (technology gaps) and will propose development plan to achieve the goal. This study will be
completed by beginning 2002.
Hydrate plug removal guidelines:
This set of guidelines is an extension of recommendations listed in the Offshore Hydrate
Engineering Handbook (Sloan 1998).
1. Hydrate plugs are always dissociated, but the time scale is usually days to weeks. Deliberate
changes and patience are required. Hourly changes are ineffectual.
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2. Multiple hydrate plugs should always be assumed and treated as a safety hazard.
3. Many hydrate plugs are porous and transmit pressure easily while acting to obstruct flow. Some
plugs are permeable to gas, but less so to condensate or black oil. This concept controls many
aspects of hydrate dissociation, including radial depressurisation, Joule-Thomson cooling through
the plug, and the fact that depressurisation may cause the temperature downstream of the plug to
decrease below the hydrate equilibrium temperature.
4. Methods are not well defined for locating hydrate plugs and determining their length. However,
knowledge of the precise location and length of a plug would be a vital help in dissociation. The
current model does not require a plug length, but this information is necessary to determine how the
pipeline can be depressurised safely.
5. Attempts to "blow the plug out of the line" via high pressure upstream always result in a larger, more
compacted plug.
6. Depressurisation from both sides of hydrate plugs is the preferred method of removal, from both
safety and technical viewpoints. This implies access points at both plug ends through dual
production lines, service lines, etc.
7. If the pressure is decreased too much, the hydrate plug will rapidly form an ice plug which may
actually be easier to remove than the original hydrate plug.
8. In a deepwater line, a liquid head on a hydrate plug may be sufficient to prevent depressurisation.
Liquid head removal is a current challenge to flow assurance.
9. In some cases, depressurisation from one side of the plug has been safely achieved.
10.Heating is not recommended for hydrate plugs without a means for relieving the excess gas
pressure when hydrates dissociate.
11.Coiled tubing represents the primary mechanical means for dissociating hydrates.
12.Usually methanol or glycol is injected into plugged flow lines, but this is seldom effective due to the
difficulty of bringing the inhibitor into contact with the face of the plug. This method is most effective
when used in conjunction with depressurisation and the hydrate plug has had a chance to recede
sufficiently from the pipe wall to allow the flow of inhibitor around the remaining plug.
13.Inhibitor injection and de-pressurising techniques are available for system shut-in and start-up two
potentially hazardous periods as regards the formation of hydrate plugs.
14.Insulated pipelines can represent a serious hindrance to hydrate dissociation. Modelling indicates
that the resistance to heat transfer through the pipe wall increases the hydrate dissociation time by
several orders of magnitude. Care should be taken when designing an insulated pipeline.
e.g. A typical overall heat transfer resistance is about 1 BTU/hr/ft/F (Sloan 1998)
This heat transfer resistance corresponds to a Biot number of about 0.02
The time it takes for the hydrate plug to completely dissociate is about 100 times greater.
At an ambient temperature of 4C, the dimensionless dissociation time changes from 75, with
no resistance to heat transfer, to 660 at a Biot number of 0.02.
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Organic Deposits
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3. ORGANIC DEPOSITS
3.1 WAXES
A deposit of waxes on the wall. As soon as the deposit forms on the wall, a process will begin
whereby its thickness will increase over time, with an impact on the pressure profiles (increase in
pressure drops inherent in the reduction in cross-section) and temperature (improvement of
thermal insulation due to the deposit). The restriction in the passage may be highly substantial, to
the extent of all but plugging the pipeline.
However, operational problems are likely to be encountered much earlier than any significant
restriction or sticking. The waxy layer indeed can be rough, increasing the surface roughness of
the pipe wall. The resulting increase in friction pressure can effectively choke the system, resulting
in higher pumping costs or reduced throughput.
Gravity settling in lines can occur during shutdown, but in this case the deposit remains very soft
and is easily removed under flowing conditions when the line is restarted.
Congealing occurs in the form of gel when production is stopped due to an increase in viscosity.
This phenomenon is quite different to the previous one but can also lead to obstruction of the liquid
flow in the event of prolonged shutdown. This aspect is explained in greater detail in section 2.4
of this guide.
The risks associated with wax deposits on the wall are as follows:
Plugging of flowlines, especially during pigging operations.
Plugging of tapping points (pressure measurement).
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The position and the speed of the wax deposits in the lines depend on the properties of the fluid, the
thermal conditions (wall temperature & gradient) and the flow rate. For Single-phase liquid systems,
the mechanisms involved are almost fully explained .
They are less completely understood for multiphase systems.
In all cases, the ageing effect (change in consistency) and influence of internal pipe surface are never
taken into account.
Deposition is a lengthy phenomenon. The speed of growth is generally slow and must be considered
as an equilibrium related to the steady flow. Deposition under short transient situations is never an
issue as the return to steady state conditions will eliminate its consequences.
The proportion of waxes deposited and adhering to the walls is small in comparison with the waxes
that crystallise in the crude oil.
For there to be a deposit, the wall temperature needs to be lower than both the Wax Appearance
Temperature (WAT) and the flowing temperature.
This is a requisite condition but is not sufficient insofar as some lines operated in this situation show no
deposits. The phenomenon has not yet been explained.
Three mechanisms can contribute to the transfer of waxes to the pipe wall:
Molecular diffusion
Turbulent diffusion of crystals (shear diffusion)
Sedimentation.
On the other hand, turbulence in the flow regime produces shearing stresses likely to tear away the
wax deposits.
As a first approximation, the rate of deposition in a pipe will depend mainly on molecular diffusion and
thus be closely related to the thermal gradient on the wall.
In addition:
a low temperature gradient will lead to a hard deposit forming over a long period while,
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We concluded that both surface and downhole samples had been polluted by the drilling mud (oil
based).
Paraffin distribution
0.3
0.25
% Weight
0.2
0.15
0.1
0.05
0
Carbon number
MDT sampling:
MDT samples can be polluted by oil-based mud. The extent of the pollution of the oil sample can be
assessed from a sample of the mud itself.
As an example, the graph above shows the paraffin distribution obtained on a Dalia 5 MDT sample.
We know that the Dalia crude contains no paraffin. The left part of the graph represents the paraffin
distribution of the base oil used for the drilling. The right part represents the distribution of heavy
paraffin, probably a deposit from previous drilling on a well where the crude contained a significant
amount of paraffin. The WAT measured on the sample was 26C instead of the usual 7-10C value for
the Dalia crude.
Surface samples are acceptable, providing the clean-up phase is sufficient to eliminate the mud
pollution.
Analysis
In addition to "conventional" PVT analyses, the evaluation of the wax potential of a crude oil requires
additional information:
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Part 1 Physico-chemical
detailed compositional analysis by Gas Chromatography (GC) up to C10+ or C20+ (about 300 crude
oil components are identified),
distribution of n-alkanes (n-paraffins) from C15 to about C50 by HTGC (High Temperature Gas
Chromatography).
The general appearance of the HTGC curve shown below allows a first evaluation of the risks
related to crude oil.
A crude oil with a lot of "light" paraffins (< C30) is likely to give rise to rheological problems that can
go as far as gelling in the shut-down phase.
A crude oil with few light paraffins but a significant number (more than 0.5% weight) of "heavy"
paraffins (> C30) will be more likely to form deposits.
n-Paraffindistribution
Nparaffin wt %
0,7
The distribution of) super heavy nparaffins (up to C80) can, in most cases,
be calculated by applying an exponential
correlation in order to reproduce the
general distribution trend given by
measurements (see calculated curve on
the right). Sometimes the n-paraffin
distributions
do
not
exhibit
an
exponential decay with increasing
carbon number ( i.e. AKPO crude). In
that case extrapolation is not possible.
0,6
%
w
e
i
g
h
t
0,5
0,4
0,3
fig 1
%weight
calculated
0,2
0,1
0
13 15 17 19 21 23 25 27 29 31 33 35 37
carbonnumber
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Part 1 Physico-chemical
180
160
as 140
120
100
80
60
40
20
0
32
Wax
No Wax
34
Bubble
36
38
WAT C
42 (C)
40
18
16
14
Waxy
Light
12
10
2
0
-25
-2
-5
15
35
55
75
95
115
135
Temperature F
3.1.3 Methodology
Based on the previous data recovered, evaluation of the wax deposition risk generally involves two
steps:
1. Use of a thermodynamic model to determine the WAT and the crystallised fraction in
relation to temperature. The model is generally based on a measurement at atmospheric
pressure and allows the prediction to be extended to all pressures and compositions.
However, the validation of input and output data is still a developing science. It is therefore
recommended to seek expert advice.
2. Use of a kinetic model to evaluate the thickness and location of the deposit in the pipelines
(cold wall deposits) versus time. It has to be stressed that this type of model is more
providing a trend of profile and magnitude of the problem.
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Part 1 Physico-chemical
Models
Most market models are based on the assumption that the deposit builds up by molecular diffusion.
The software used in studies is:
An integrated (thermodynamic + thermal + multiphase flow + deposition kinetics) model, TUWAX, developed within the framework of a JIP by the University of TULSA. This is a two-phase oil
and gas model and does not take the water phase (assimilated to oil) into account. From a given
composition, it will determine:
1 the phase envelope, to be tuned on PVT data,
2 the change in viscosity vs. temperature, to be tuned with laboratory measurements,
3 WAT, to be tuned on the value given by DSC,
4 After validation / calibration of the 3 measurements, the thickness of the deposit
versus time along the production line.
dF dT
dQ
=
dt
dT dy
c
where:
dQ/dt
Fc
T
dy
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Part 1 Physico-chemical
Laminar
Boundary
Layer
Turbulent core
Dissolved wax
Heat Loss
P
I
P
E
W
A
L
L
Velocity profile
Rippling only plays a preponderant role when shearing is significant, that is generally the case when
the pipeline is close to plugging. TU-WAX makes allowance for this effect with a shear factor. But it
should be noted that the shear influence has never been validated by experimental data.
The practical consequences of these assumptions are as follows:
Deposition will not occur if the external temperature is greater than or equal to the crude oil
temperature,
If the wall temperature is close to that of the crude oil, the kinetics for deposits will be
relatively insignificant (case of an insulated pipe),
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Part 1 Physico-chemical
12
Thickness (mm)
6 hours
1 day
2 days
3 days
4 days
5 days
6 days
7 days
6h
Inlet TC=54C
10
8 Inlet TC=25C
6
4
2
0
0
10C
1,5
20C
30C
0,5
% weight
0
30
35
40
Carbon Number
The higher the temperature (but < WAT), the greater the molecular weight of the deposit will be. Since
Paraffin deposits as a solid solution, the composition of the deposit at high temperature will be different
from that for deposits generated at temperatures close to ambient temperature.
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Shearing effects due to flow turbulence will also be preponderant in the formation of deposits. The
mechanical forces generated by flow act on the pipe wall and affect the quantity of waxes that adhere
and remain in the deposit layer. Under a turbulent regime, the most "tenacious" waxes will adhere to
form a hard deposit.
However it is highly important to note, for practical operation, that commercial software does
not provide any information on the quality of wax deposits.
Finally, the flowrate influences the thermal gradient and the shear effect. The general trend can be
represented as below:
Deposition rate
Turbulent
Laminar
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3.1.4 Solutions
Wax is generally assumed to be easily prevented or removed by a combination of thermal and
mechanical solutions.
As pointed out above, the driving factor in wax deposition is pipe wall temperature, and its kinetics are
mainly dependent on existing gradient and shear effect.
Prevention
2 types of action can be implemented to prevent wax deposits on cold walls:
chemical
thermal.
Chemical solutions
Chemical additives act by limiting the agglomeration and growth of crystals (dispersing effect). They
are never completely effective and are mostly used to assist mechanical removal (pigging or scraping).
Their cost is not to be underestimated, due to the high concentrations that have to be injected.
Another chemical means worthy of mention is film-forming additives (Anticor, CECA), which work on
principles similar to those of a corrosion inhibitor, forming a film on the pipe wall deterring the wax
crystals from adhering to it. This type of product is currently being evaluated. Suppliers claim near to
absolute efficiency but this remains to be proved.
Today, due to the limited efficiency of present additives, chemical treatment cannot be envisaged as
sole prevention method. Chemical means are mainly injected in order to decrease the curative
treatment frequency.
Thermal solutions
Simple (passive) or more complex thermal insulation is used to maintain temperature above the WAT.
There are a variety of thermal insulation solutions, like bundles, pipe in pipe, pipe coated with insulating
foam, etc.
Monitoring
In-situ monitoring of wax deposits has so far not been industrially proved. However, different
parameters can be monitored and analysed to deduce how the deposit will evolve:
pressure losses in the different sections, from monitoring of discrete pressure measurements
(well head, manifold, riser and top side arrival). ). It has to be highlighted that pressure losses
could be mainly affected by the increase in roughness which will dominate the frictional
pressures long before any consequent reduction in pipe diameter.
temperature along the line, which can be measured using an optical fibre in contact with the
pipe wall
spot measurements of thermal flux through the pipeline (under development).
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Part 1 Physico-chemical
Curative treatment
1- Thermal
To melt deposits, rapid cleaning of the lines with heat is not realistic because it requires much higher
temperatures (generally around 70C) than the WAT.
However, heating the wall to a temperature slightly higher than the WAT can change the structure of
the edges of the deposit, rendering it more prone to tear-off by turbulence. This solution is being
evaluated within the framework of a JIP aimed at qualifying a PIP insulation system, equipped with an
electrical heating device.
2- Mechanical
Pigging has two functions:
mechanical destruction and elimination of wax and any other deposits that have settled in the low
points (i.e. corrosion products)
separation of fluids for hydrate preservation procedures applied with respect to hydrates by
circulation of stock-tank oil.
Pigging frequency can be determined from simulation results and data acquired during pigging
operations (delta P, quantity recovered at the pig receiver, number and length of production
shutdowns, etc.).
Costs
Plugging Risks
12
Intervention No.
One absolute requisite for Deep Offshore pigging is control over the speed and position of the pipeline
scraper in the lines. Cleaning may be improved by the jet effect (Spider nose type bypass system), by
control over the pig speed (Vmin. 1.3 to 1.5 m/s) and by the choice of a suitable design (two-way,
detectable and destructible).
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Loop arrangement, with both departure and arrival trap located on topsides and two production
lines connected together to form a loop. During the pigging phase, one of the two branches
produces in reverse direction and some wells are either shut down or have their flow rate reduced.
A fluid is pumped from the surface to provide energy.
Arrangement in a single line equipped with a subsea pig launcher (SPL). To reduce operating
costs for installation and removal of the SPL, several pigs are stored ready for use in a cassette (5
to 10) on the pig trap. SPL have been selected by BP on ETAP (GD engineering concept) .
Same approach has been adopted by Shell on two GOM satellite fields: Serrano and Oregano
(Oceaneering concept) tied-back on AUGER.
3- Chemical
The use of solvents is not very effective unless considerable quantities are injected, as heavy waxes
do not readily dissolve in most conventional solvents. Aromatic solvents (toluene and xylene) are the
least bad. They can be doped with dispersants to improve the dissolution kinetics.
Commingled chemical and thermal cleaning (Petrobras SGN process) is to be kept for desperate
cases. The major difficulty is injecting the chemicals close to the plug location.
A chemical/mechanical combination is sometimes needed to limit risks of plugging. The injection of a
batch of solvent upstream of a pig softens the deposit.
Conclusions
The most frequently adopted solutions are:
Non-piggable zones (wells, jumpers, manifold) are kept outside the deposition temperature range
with appropriate insulation for normal and specified low flow conditions.
Flow lines and risers are likely to be in the same situation. Nevertheless, the production loop
arrangement or single line associated with sub-sea pig launcher system can tackle any issues,
especially when deposition occurs in certain downgraded conditions such as very low flow-rate or
insulation deficiency.
Continuous chemical injection should be considered only as an ancillary means needed to lower
pigging frequency.
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3.2 ASPHALTENES
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when mixing two fluids, usually an asphaltenic crude oil with a paraffinic hydrocarbon, or sometimes
with the injection of gas.
During CO2 flooding.
Some cases of asphaltene floculation in the near wellbore area are also reported during stimulation
jobs (well acidification).
Asphaltenes floculation can deposit in reservoirs, on wall of tubing or flowline, and decant in
separators. Deposits can interrupt partially or totally the Production due to the formation of plugs.
Flocculated asphaltenes take a very long time to re-dissolve by re-pressurisation.
The simple re-dispersion of asphaltenes flocculated and decanted in a tank is almost impossible.
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Part 1 Physico-chemical
Characterisation of asphaltenes by dilution lines.
Distribution of saturates, aromatics, resins and asphaltenes, (SARA), on heavy fractions (C15+),
detailed compositional analysis by Gas Chromatography (GC) up to C10+ or C20+ (about 300 crude
oil components are identified),
Pressure and temperature profile of the stream from the reservoir up to the separator,
Change in the reservoir pressure over time, pressure profile in the near wellbore area.
Floculation point can be, in some cases detected using a light transmission measurement, this
method is internally available for atmospheric conditions and need specific procedures for some
fluids.
3.2.3 Methodology
Risk prediction
Natural flocculation is difficult to predict. The existing thermodynamic models are poorly suited to this.
A rough evaluation of the asphaltene risk is however possible using the characterisation data for
asphaltenes, the crude oil and the production parameters for a given field.
At this stage, if a possible risk has been identified, it will then be necessary to perform laboratory
experiments under Operating P & T conditions, on a downhole sample as defined above.
HPLC column
High Pressure Liquid chromatography
filter
fluid
fluid
Sapphire window
P
Injection point
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The bottomhole sample is depleted in the PVT laboratory by transferring the fluid from 2 cells. The
transfer line is equipped with a filter, a sapphire window and video microscopy. Flocculation is detected
by a combination of:
Video microscopy observation,
Analysis of the pressure drop on the filter edges,
Quantification of the asphaltenes remaining in the filtrate,
Characterization by chromatography HPLC (high pressure liquid chromatography).
Another detection has been developed based on laser detection. This method is not
internally used.
It should be noted that most known asphaltene problems are discovered a posteriori during field
operation.
The same approach must also be followed when reservoir gas injection is performed. It may
lead to asphaltenes deposits either in the reservoir or in the near well bore of the production
well.
In particular, if the injected gas is CO2 or a concentrated acid gas Asphaltenes flocculation is
widely enhanced.
However, when the flocculation occur far from the near well bore it does not seem to damage the well
productivity.
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3.2.4 Solutions
Preventive chemical treatment in the well bore is reserved for special cases. Squeezes of solvent +
dispersant mix are used to clean the near wellbore area (HASSI MESSAOUD) but their efficacy for use
in prevention is dubious due to the limitations of adsorption on the rock. They are not very realistic for
Deep Offshore fields.
Chemicals have to be improved for preventive application. They are poorly adsorbed on the formation
rock and conversely need to be present at high dosage in the fluid to be efficient.
Reservoir management (pressure), when possible, is the only available method to prevent deposits
near the wellbore area.
Increasing or decreasing the well bore pressure shifts the location of asphaltene formation to inside the
reservoir where it has no influence, or to the tubing where it can be chemically controlled.
If flocculation occurs inside the tubing, down hole chemical injection is the best practicable solution.
Additives for this come in two types:
The first type is intended to retard flocculation or reduce the quantity precipitated.
The second type (the most frequently used and most effective) is intended to disperse the
asphaltene flocculates and keep them in suspension so they can be carried away (case of
LAGRAVE).
Mechanical methods can be used to remove periodically asphaltenes deposits. Asphaltenes can be
more brittle and harder to remove than typical wax deposits. If they form in the near wellbore area
mechanical removal is impossible.
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3.3 NAPHTENATES
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Part 1 Physico-chemical
Partial pressure of CO2 under reservoir condition,
Reservoir P & T
3.3.3 Methodology
The main factors affecting the formation of naphtenates are:
The calcium content of the water, expressed in milli-equivalents per litre (meq/l),
The water bicarbonate content. This value is calculated from the partial pressure of CO2 in the
hydrocarbon, expressed in meq/l,
To evaluate the naphtenate risk, known as PHA (Potentially Hazardous Acids), we retain the lowest of
the values (meq/l) for these 3 parameters. This value represents a qualitative definition of the level
of risk (see table below).
Field
TAN
Acids
(meq/l)
HCO3
(meq/l)
Calcium
(meq/l)
PHA (meq/l)
DALIA Prod
1.4
100
18
150
18
DALIA Inject
1.4
100
21
48
21
GRYPHON
4.5
321
12
93
12
HEIDRUN
2.8
200
11
55
11
ALBA
143
10
29
10
IME
2.1
150
29
AFIA
1.2
86
51
Following previous definition, DALIA is, to date, the most severe case, but the naphtenates risk is
limited by the 18-meq/l bicarbonate content, despite an acid content of 100 meq/l (TAN = 1.4). This can
be compared with the least severe case of IME which, despite an acid content of 150 meq/l (TAN =
2.1), has a limiting factor of 4 meq/l due to the water calcium content.
Evaluation of the risks of deposits is still at the R&D stage.
We are currently studying the influence of the molecular weight of acids on problems of production
(deposits or emulsions).
We are performing three types of tests:
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Part 1 Physico-chemical
Below, we can see the differences in distribution between four different samples of oil.
ACID DISTRIBUTION
1
0.9
0.8
0.7
0.6
TA
N
Dalia 3
Dalia2
0.5
Bilondo
Orchidea
0.4
0.3
0.2
0.1
0
0-150
150-230
230-350
350-400
cut
400-550
550+
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Part 1 Physico-chemical
By studying the decantation of water in a Bottle Test for different pH values (adjusted with Sodium
hydroxide), it is possible to calculate the quantity of acid transferred into the water phase and the pH
value at which the emulsion became stable, and thus determine the ideal pH value at which to perform
water-oil separation.
The graph below shows decantation performances vs. pH values.
As an example, for DALIA 1, when pH is greater than 6.2 6.4, the emulsion becomes very stable
causing separation difficulties.
very stable
emulsion
100
TANc=0.86
TANc=0.22
TANc=0.29
90
TANc=1.4
TANc=0.11
TANc=1.1
80
TANc=0.045
70
TANc=0.23
60
TANc=0.33
DALIA2
50
DALIA1
40
30
TANc=0.032
TANc=0.086
ORQUIDEA
TANc=0.56
unstable
emulsion
20
10
TANc=0.022
TANc=0.014
TANc=0.062
TANc=0.024
TANc=0.25
TANc=0.01
0
4
10
11
12
13
14
final pH
3.3.4 Solutions
The pH can be controlled either by adding acetic acid or by increasing the separation pressure that
limits the release of CO2.
1- The easiest way to deal with the naphtenate problem is to deliberately lower the pH of the crude oil
by acid injection.
The most often used is acetic acid (low cost), but hydrochloric acid (handling problems) or formic
acid (better performance but high cost) can also be used. Acid injection has to be carried out with
care since asphaltene floculation/precipitation can arise.
The dosage can vary from 100 to 500 ppm (for fields in Nigeria and Cameroon, 300 to 400 ppm
predicted for the Miocene reservoirs on Block 17).
2- Since the pH of the solution is directly related to the pressure, the formation of naphtenates can be
eliminated by separating water out under pressure (10 to 20 bar).
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3- For naphtenate deposits forming at a high pressure (> 20 bar), demulsifier can be injected as a
dispersant to prevent deposits in the production stream.
4- As additional back-up, the following curative treatment can be implemented:
to fit the separator with an interfacial collector able to draw out the accumulated emulsion pad
to clean the naphtenate soap decanted on the separator/tank bottom using heated water
jetting.
To inject batch of acid.
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Scale
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4. Scale
The water produced undergoes changes in temperature and pressure throughout the production
stream. The solubility of certain inorganic components of water can then decrease and form
deposits by precipitation.
When two incompatible waters are blended, precipitation of inorganic salt(s) may occur. This is the
case with reservoir water containing barium mixed with sea-water (injection water) containing
sulphate. It may also occur when reservoir water containing calcium is mixed with a completion or
stimulation fluid made from sea-water or containing acid (HF or HCl).
CARBONATE
Carbonate deposition results from the variations in solubility in relation to pressure and temperature.
When pressure drops, the CO2 dissolved in the water tends to be released, thereby decreasing the
solubility of the carbonates.
Unlike most mineral deposits, carbonates have inverted solubility, meaning that when the temperature
rises, their solubility decreases. Conversely, when the temperature drops, their solubility increases.
Generally, reservoir waters are in equilibrium with calcite, the most common carbonate. Risks of
carbonate deposits will depend mainly on the pressure and temperature conditions the fluid will
encounter. When pressure drops, the risk increases, but when the temperature drops the risk
decreases.
A fluid that is rapidly decompressed while its temperature is maintained will thus produce carbonate
deposits (e.g. ESP). Conversely, a fluid that cools quickly will not form deposits.
For example, thermal insulation of deep water pipes to avoid wax deposits may lead to carbonate
deposits that would not have formed under a conventional development, as the temperature in this
case drops more slowly than the pressure.
The main carbonate deposits are calcite and aragonite (calcium carbonate deposits).
Siderite (iron carbonates) may also be encountered, generally resulting from corrosion.
Other, rarer forms exist, such as witherite (barium carbonate), encountered in HP-HT or vaterite, which
is a rarer form of calcium carbonate.
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SULPHATES
Sulphate deposits are most often due to incompatibility between the reservoir water and another fluid
such as injection water or stimulation fluids. Reservoir waters may contain significant quantities of
calcium, strontium and barium.
Calcium sulphate is highly soluble and deposits are therefore seldom encountered. The most
common forms of calcium sulphate are gypsum and anhydrite.
Some reservoir waters have a very high calcium content (e.g. Persian Gulf oil production, Torpille in
Gabon or N'Kossa in Congo). In this case, deposits of calcium sulphate may form by mixing with
injected sea-water (reservoir pressure maintenance).
One may also come across deposits of calcium sulphate following acidification in a reservoir containing
carbonate or dolomite, if the residual fluid encounters sulphated water, either sea-water or the reservoir
water itself. For example, some dolomitic reservoirs have a reservoir water highly charged with
sulphate.
The solubility of strontium sulphate is intermediate between those of calcium and barium sulphate. It
is often combined with barium sulphate scale.
The solubility of barium sulphate is negligible, around a few ppm. Any contact between a reservoir
water containing barium with a water containing sulphate results in the formation of barite (barium
sulphate). The incompatibility of sea-water, which is generally used to maintain pressure with reservoir
barium laden waters, is a serious problem as soon as the barium content exceeds a few tens of ppm.
It becomes a critical problem as soon as this barium content rises above 30 ppm (i.e. 30 40 ppm
starts to be a problem on Brent fields).
Above 300-400 ppm of barium, a feasibility and economical study should be carried out to recommend
the most cost effective treatment.
SILICA
Silica deposits are not encountered in oil production on conventional developments. However, this
phenomenon may occur when re-injecting produced water from a sandstone reservoir at high
temperature. This can happen indeed, with EOR (steam injection) but also with deep HP/HT
production.
Sandstone reservoirs are in equilibrium with quartz. At high temperature (T> 130C), the silica content
of the production waters will be such that the if the temperature drops below 20C, amorphous silica
may be precipitated.
SALT BRIDGES
Salt deposits may occur when liquid reservoir water evaporates in the gas phase under bubble point
pressure or for very salty waters due to variations in solubility associated with the drop in temperature.
The most common deposits due to evaporation are Halite (sodium chloride) and anhydrite (calcium
sulphate).
Note also that adding methanol (hydrate prevention) reduces the solubility of salt (NaCl).
On waters close to saturation (salinity around 300g/l) the injection of methanol may lead to massive
precipitation of salt.
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Certain isotope ratios that may also help in validating samples, such as hydrogen / deuterium,
oxygen, strontium and boron. Analysis are generally used by geochimists.
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Part 1 Physico-chemical
4.3 Methodology
Prediction
CARBONATES
Based on available water analysis, prediction is conducted with the in-house model: SCALE 2000. Its
validity range has been extended to temperatures higher than 200C and high salinity (300 g/l). The
model was developed in co-operation with the BRGM (Bureau de Recherche Gologique et Minier).
At a given pressure and temperature with water and gas composition, the model determines the
Saturation Index (SI) of the water.
IS=0,5
IS=1
IS=2
1,50
Real profile
T/To
1,00
0,50
Downhole
0,00
0,00
-0,50
0,10
Surface
0,20
0,30
0,40
0,50
0,60
0,70
0,80
0,90
1,00
P/Po
-1,00
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Part 1 Physico-chemical
On the graph above, the brown curve represents the evolution of T/To and P/Po pairs from down-hole
to surface facilities (real profile). Po and To correspond to reservoir conditions.
Other curves represent different iso saturation index profiles: SI = 0 - 0.5 - 1 and 2.
The relative positioning between these curves and the real profile gives the scaling potential all along
production stream.
The SCALE 2000 model includes a kinetic module to determine precipitation quantities versus time
and thereby obtain a deposit thickness for a given water production.
g of deposit / Kg water
Calcite
0.045
0.04
0.035
0.03
0.025
0.02
0.015
0.01
0.005
0
0
10
15
20
25
Time (minutes)
30
35
40
45
Time
The graph above shows the quantity of "precipitable" deposits versus time. The quantity of deposits is
calculated according to the flow-rate and the velocity values in the lines (tubing, flowlines, risers).
SULPHATES
When sea-water is injected, sulphate from the sea-water will be introduced into the reservoir.
If the reservoir water contains barium and/or strontium and calcium, the risk of sulphate deposition
(barium, strontium and calcium) is maximum when a certain ratio of reservoir to sea water is reached
(see graphs here below).
Sulphate deposits in the near well bore area and inside the bottom part of the tubing will strongly affect
well productivity.
To determine the sulphate deposition risk, we use the same predictive model: Scale 2000.
At a given pressure and temperature, the model computes the super-saturation index (figure1) and
quantity of deposits for different ratios of reservoir to sea waters (figure 2).
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Production water
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Another, more realistic method takes into account the ionic equilibrium reached when the sea water
contacts either the reservoir matrix or the reservoir water:
Under certain conditions, seawater can exchange its sulphates with carbonates from the matrix.
This phenomenon significantly decreases the sulphate content of the injected water on arrival in
the near well-bore area and consequently reduces the associated risk of deposition.
The precipitation of sulphate in the reservoir when the sea-water comes into contact with reservoir
water can be evaluated by introducing a precipitation module in dedicated models (ECLIPSE
UTCHEM).
A combination of the two approaches gives a more realistic estimation of sulphate deposit risks in the
near well-bore area.
SALT BRIDGES
Salt bridges normally form under conditions of high salinity reservoir water and high reservoir
temperature.
The composition of the deposit depends on the solubility of all the salts present in the produced water
(generally halite NaCl sometimes anhydrite CaSO4)
Salt bridge formation in the well is a consequence of three different phenomena:
The tendency of soluble water in liquid hydrocarbon to separate when temperature drops.
While the first two tend to favour the formation of salt bridges, the last phenomenon generally
eliminates the risk.
Thermodynamic models are used to simulate the separation of the water into the gas phase, the oil
phase and as a separate aqueous phase.
Modelling generally indicates a risk when the total water cut does not exceed a few percent of water.
4.4 Solutions
CALCIUM CARBONATE deposits
Carbonate deposits are generally controlled by continuous downhole injection of a suitable scale
inhibitor.
Due to the low seabed temperature and associated high viscosity of the chemical, a solution is made
with MEG, thereby serving to inhibit hydrate formation in the injection line as well.
Where such prevention fails, remediation is usually possible by acidifying the tubing through the
service line.
SULPHATE scaling
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Downhole chemical injection for carbonate scale is usually fairly efficient in curbing sulphate scale,
providing the chemicals are injected at sufficient dosage and frequency. This can be used to protect
tubing and production stream from deposition.
However, if risks have been identified in the well-bore area, other solutions must be considered to
prevent deposition:
Water other than sea-water may be used when possible, providing its sulphate content is suitable
Gas injection can replace water injection, thereby obviating any incompatibility
For deepwater wells, sulphate removal will generally be the wisest choice. The residual sulphate
content should be around 40 ppm, in order to considerably reduce the risk in the tubing and
eliminate the risk in the near well-bore area.
Even though performing squeezes in deepwater wells is a difficult challenge, this solution must be
examined, especially for satellite fields. It can prove economical compared to sulphate removal.
This is the case when water breakthrough occurs late in the field life, and when squeeze efficiency
is demonstrated on the concerned wells.
Downhole injection of chemicals below the perforations may also be an answer. It has never yet been
applied, due to technological limitations and reduced confidence in its reliability.
When a risk of calcium sulphate deposits has been identified, reservoir management is the only
preventive method. Clearly, it is not recommended to produce a level with sulphated water at the
same time as a level producing water containing calcium. The quantity of deposit precipitated can
be so vast that no preventive or removal methods will be economically feasible.
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Miscellaneous Problems
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Part 1 Physico-chemical
5. Miscellaneous Problems
5.1 RHEOLOGY
5.1.1 Definitions
Under laminar flow, the fluid layers slide one against the other. The shear rate is expressed
by:
dv
, where dy is the distance between the layers.
dy
A surface element in a layer requires a force df to slide along the adjacent layer. Shearing stress is
known as the value such that
df
.
ds
dS
v
dy
df
For a non-Newtonian fluid, the shear stress can be any function of the shear rate. Nevertheless, by
analogy with Newtonian fluids, one terms apparent viscosity a the ratio
and
. The
Paraffinic crude oils are non-Newtonian at low temperature. The usual hydrodynamic models such
as Olga, Prosper, Tacite and others, cannot handle such fluids.
At a temperature close to or below their Pour Point, the rheology of the paraffinic fluids shows a
yield value. This means they do not flow in a pipe until a certain pressure has been applied. The
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relevant pressure may be high and may exceed pressure related to the reservoir pressure or the
maximum admissible service pressure of the pipe.
Even generally Newtonian asphaltenic or naphthenic fluids are highly viscous, especially at low
temperature. The evacuation scheme must be studied in this respect.
Emulsions have a higher viscosity than that of their component fluids. The viscosity of a crude oil
containing between 50 and 70% water can be multiplied by a factor of 20.
They may be considered as Newtonian in the range of shear rates applied on standard pipes. Even
if they present a yield value (mayonnaise is an example of emulsion), it remains negligible in all the
cases encountered in oil production.
In a pipe transporting water and oil, an equivalent viscosity can be associated with the fluid if the
dispersion of one phase into the other is entirely completed. In that case, the dispersion is
equivalent to a single phase. It is pointless, highly inaccurate and even dangerous to try to tune
viscosity in a multiphase fluid flow code if the phases are even slightly separated.
5.2.2 Methodology
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capillary viscometers with imposed flow: to measure the apparent viscosity of the reservoir
fluids at reservoir conditions.
The crude oil circulates in a capillary tube at a fixed flow rate while the pressure drop is measured. The
relationship between viscosity and the pressure drop can be expressed using the Poiseuille relation.
Shearing cannot be controlled, so they are only suitable for Newtonian fluids, which is generally the
case for high temperature reservoir fluids.
variable flow capillary or "Canon Fenske" viscometers: for commercial transactions on crude
oil. These are U-shaped tubes. One of the branches of the U is filled with the crude oil. The time
needed for the levels to balance is a function of viscosity and density. Specific charts are then used to
relate this time to viscosity. The viscosity is then termed kinematic viscosity to take into account the
dependence on density.
Shearing is not checked at all, and the measurement is therefore not reliable for non-Newtonian crude
oils. In practice, commercial transactions sometimes neglect this problem.
coaxial cylinder (or cone-plan) viscometers involve introducing the crude oil between a rotor
and a stator. A rotation speed is then imposed on the rotor and the torque needed to ensure this speed
is measured. As the value of the gap is known accurately, the shearing can be reliably measured. The
relation between the torque and the rotation speed is equivalent to that between the shear stress and
the shear rate, thereby enabling apparent viscosity to be measured. The value obtained is independent
from the density and is termed dynamic viscosity.
Consequently, dynamic viscosity is equal to the ratio of Kinematic viscosity to density.
This is the only principle that can provide the apparent viscosity value for non-Newtonian fluids at
known shearing rates.
Finally, models for extrapolating atmospheric measurements to pressurised fluid are under
construction but are far from being accurate enough.
The major difficulties arise from the necessity to take into account both the influence of the pressure
itself and the light components. Naturally, these models can only simulate viscosity for Newtonian
fluids. To the best of our knowledge, any ongoing research to date aimed at including non-Newtonian
behaviour on pressurised fluids is pure speculation.
the number, size and shape, interactions and orientation of the crystals.
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The viscosity of the matrix, considered to have constant composition, will depend only on temperature.
On the other hand, the state of the crystalline fraction will be related to the temperature, but also to the
way the crude oil has been cooled. For example, by analogy with mineral crystals, we may expect slow
cooling to cause the formation of large crystals in small numbers, while conversely, quick cooling will
lead to crystallisation in the form of many small crystals.
A list of the thermo-mechanical conditions affecting apparent viscosity is given below. It is not intended
to be exhaustive, but corresponds to phenomena that have been observed in the laboratory during
research projects. It helps account for the extreme variety of parameters to be taken into account to
obtain a rheological "model" for paraffinic crude oil.
The relevant parameters are:
cooling speed,
shearing value,
presence of additive,
Each of these conditions may change the apparent viscosity of the crude oil at low temperature by a
magnitude of one or more.
Further, significant interactions between these conditions have been noted. As an example, a crude oil
subjected to shearing is normally thixotropic (viscosity decreases with time when the crude is sheared)
at low temperature but can become rheopectic (viscosity increases with time when the crude is
sheared) when doped by a wax inhibitor.
Finally, the best recommendations to follow when investigating the rheological behaviour of a paraffinic
crude are:
Cover as much as possible of the range of temperature and shear rate needed to represent the
conditions of the whole produced stream.
Use these values in the flow simulators to calculate the average shear rate in the line considered.
This last point is of course highly tendentious but should be considered for the moment as
affording the best possible guess.
Assess the yield value if the crude is likely to remain in a flow line at a temperature close to or
below its Pour Point. In this aim, , to measure the yield value during lab studies, we have to
reproduce as much as possible the the thermo-mechanical history of the fluid.
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5.2.3 Solutions
Heat tracing of all the small secondary lines likely to be frequently stopped,
Chemical injection to reduce apparent viscosity and lower the Pour Point.
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Blending with a light cut or crude oil. Compatibility must be checked before when contemplating
asphaltenic crude dilution. Asphaltene flocculation is the major drawback of such a technique
Insulation or heat tracing of the lines, or re-heating station on long distance pipes
There are no chemical solutions. Even conventional Drag Reducer Agents cannot be used since, with
such high viscosity, the flow regime is not turbulent.
Production of heavy asphaltenic crude oil in deepwater condition should be a severe technical
challenge.
5.3.2 Methodology
The apparent viscosity of an emulsion is easy to measure in the laboratory at atmospheric pressure on
a coaxial cylinder viscometer. It has been standardised for water cuts from 0 to 100% in a single test.
Close to the inversion point, the emulsion is often not stable enough to avoid oil, emulsion and free
water segregation into the coaxial viscometer. In fact, what is actually measured is the viscosity of a
complex mixture of free oil, free water and only a part of emulsion. That behaviour is shown is the
following curve.
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Part 1 Physico-chemical
Of course, if the oil itself is non-Newtonian, it is safer to take the measurement at the required shear
rate.
Some people use empirical laws to assess the viscosity of an emulsion according to its components
and their volume fraction.
The best known, used in SHG internal code is Eilers' law:
a
(
)
= e 1b
0
, where:
In theory, viscosity can increase infinitely for values corresponding to the more compact stacking of the
drops, such that the smaller the size of the dispersed phase particles, the greater the coefficient a will
be. In practice, laboratory measurements show that the coefficient for increase does not exceed the
value 20.
Using standard formulae to calculate the viscosity of emulsions often proves a highly conservative
approach. We generally consider that their validity range is limited to water contents of the order of 35
to 40%.
/ model.
/ meas.
25
20
15
10
5
0
0
20
40
60
BS&W
80
100
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Part 1 Physico-chemical
5.3.3 Solutions
Chemicals shift the inversion point towards low BS&W (see DALIA curve below). With constant
composition, the viscosity of the emulsion will thus approach that of water.
8
7
INVERSION POINT
6
5
WITHOUT
CHEMICALS
/ meas.
/ meas.
3
2
WITH
CHEMICALS
1
0
0
20
40
60
80
100
BSW
The pressure drop in two-phase oil/water lines is thus strongly reduced by injection of demulsifier.
Tests performed by ELF CONGO and ELF GABON show that injections in wells by gas-lift can have a
highly beneficial action on their productivity. The gains observed (see graph here after) vary according
to the case by between 20 and 50% of the well production. Some cases (Tchiboula) seem to be even
more favourable.
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Behaviour of well TBM 210 with and without injection of demulsifier via gas-lift
The ideal situation is with paraffinic crude oil, BS&W 40 to 60%, and a temperature at wellhead lower
than the WAT.
Indeed, not only does the product improve the viscosity of the fluid in the tubing but this action also
stabilises the fluid flow while avoiding slugs. The effectiveness of G-L is thus significantly improved.
The precautions to be taken are as follows:
Check that the product can be injected into the gas-lift (evaporation of the solvent may cause the
formation of gums and plugging of the annular pressure response safety valve or even the G-L
valve).
In most cases, the product can be injected diluted at 50% in gas oil, a heavy alcohol or a glycol,
thereby completely eliminating the risk of gum formation. This technique also allows for better
dosage of the product.
Inject a plug of solvent to saturate the annular space before introducing the demulsifier
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5.4.1 General
Even though not directly related to deepsea production, emulsion separation is often included in a Flow
Assurance study because of its strong relation with the other potential issues, and its clear interaction
with the development process scheme.
5.4.3 Methodology
Two types of tests are generally performed:
Static bottle tests to compare the oil to be produced to already known cases
Dynamic decantation tests on a pilot rig to assess the efficiency of decantation in conditions as
close as possible to those of the actual field situation.
5.4.4 Solutions
Decantation issues can seldom be prevented. The only known case concerns crudes containing
naphthenic acid. It has been proved that pressurised separation to keep the acidity of the water below
a critical pH is sometimes highly beneficial.
Most of the time, once the risk is established, the installation has to be specially designed.
There are numerous devices devoted to water separation. Most common are:
3 phase separator
FWKO,
Continuous separation tank,
Batch separation tank,
Wash tank,
Treater heater,
Electrical dehydrator
Centrifuge,
In addition to these physical devices, different solutions can be envisaged, alone or combined to
increase their efficiency.
Basically, the solutions are:
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Chemical - by injecting additives upstream of the separator. In this case, even though additives
can be roughly pre-selected in the laboratory, it is better to opt for on-site testing.
A number of more exotic solutions may be possible for individual cases such as re-circulating the
decanted water in order to separate a direct emulsion (oil in water). This drastically reduces the
viscosity of the external phase thereby decreasing decantation time. This possibility is particularly
well suited to the separation of heavy viscous crudes.
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The productivity,
Then, at a preliminary stage, parametric flow studies are performed, with sensitivities to the following
basic data:
Environmental data
Fluid properties oil, gas and water, and flowrates
Reservoir pressure and temperature, Productivity Index
Geometry and mechanical design of wells, mud-line and risers
Development scheme phasing, number of producers.
Process parameter of the topsides.
The number of parameters affecting the flow behaviour requires a systematic parametric simulation
approach which can be eased by the use of efficient simulation management technique, allowing to run
and interpret hundreds of sensitivity cases in a limited amount of time.
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The physical properties of the fluid which are both pressure and temperature
dependent.
As for the productivity calculations, integrated hydrodynamic and thermal calculations are required,
based on a pre-screening of the overall heat transfer coefficient profile along the various parts (well,
mud-line, riser) of the production system. Refer to the Thermal Management theme.
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6.3 METHODOLOGY
Simulation tools
Transients as Stability and Cooldown behaviour are evaluated with OLGA 2000.
In case of Steady-state and transient simulations combined in the same study, for example for
quick evaluation of developments, OLGA 2000 is used through out.
In case of segregated flow conditions, the slippage between the oil or condensate and the water
phase plays a important part and a three-phase flow approach must be considered. The Water
option of OLGA 2000 is then used.
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The objective of these calculations is to evaluate productivity constraints in order to size the diameters
of the flowlines.
Line pressure drop and well performances are calculated using:
-
Thermal module: Steady-state heat transfer between the effluent and the ambient media are
calculated with a given U-value (W/m2.K) profile along the various parts of the network (well
tubing, flowline and riser (see Thermal Management theme).
Note that flow simulators usually refer the U-value to the inner steel pipe-wall (noted Ui ), whereas
software used for pipeline mechanical design refer the U-value to the outer steel pipe-wall (noted
Uo). Moreover the later do not include the internal convection factor in the Uo calculation and
assume an infinite external convection factor.
To summarize, the thermal resistance of the insulation layers only is accounted for the evaluation of
Uo. It is therefore of some importance to clearly state the reference surface (inner vs outer pipe wall
surface) when mentioning U-values and to indicate whether this U-value accounts for
external/internal heat convection.
An example of inflow and outflow performances is given on the graphs here after for water cuts of 0
and 40%.
400
375
350
325
6 " ID
300
8" ID
10" ID
275
11" ID
IP = 50
INFLOW Performances
250
IP = 75
IP = 200
225
IP = 380
200
175
OUTFLOW NEEDS
for a given length
150
125
100
0
5000
10000
15000
20000
25000
Liquid Flowrate (bopd)
30000
35000
40000
45000
50000
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400
375
350
6 " ID
8" ID
10" ID
325
11" ID
IP = 25
300
IP = 50
IP = 100
275
IP = 140
250
225
200
175
150
125
100
0
5000
10000
15000
20000
25000
30000
35000
40000
45000
50000
The line diameter is chosen according to these results, taking into account the decrease in pressure
losses and associated increase in flow transport capacity.
The flowline diameter is selected as the minimum diameter providing the required flow capacity and
compatible with the available wellhead pressure. Given the present incertainty of the hydrodynamic
models, in particular in high riser applications, it recommended to apply some design margin
(tentatively, 10% in case of well defined fluid and well known topography, to 20% otherwise) on the
calculated pressure drops.
We have to consider also stability and erosion/corrosion issues (see 6.3.2 and 8
Erosion/Corrosion).
Erosion Corrosion) using a common criterion (API RP14E with a C factor of 130 to 170 in absence of
solid particles). If a gas breakthrough occurs, erosion/corrosion could become a governing factor and
consequently lead to choosing a larger diameter line.
From a productivity standpoint, a deeper configuration with a sufficient increase in water depth is
beneficial compared to similar developments with a shallower water depth:
at low water cut, pressure losses are mainly due to the column weight, and a higher
GOR is quite beneficial
at high water cut, a gas-lift injection point at the riser base is more efficient compared
to a shallow injection location.
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The objective of the prediction is to evaluate potential production problems caused by unstable flow
regime in the riser and which may lead to severe slugging, and also to determine and quantify the
flowing parameters involved in this phenomenon.
It should be noted that transient simulation results are fairly sensitive to many inputs. Therefore an
stability study should not be based on a fixed set of inputs but should deliver sensitivity to the inputs.
The distribution of slug characteristics (lengths, hold-ups, velocities, frequencies) is of a statistical
nature. It is not reasonable to size the topside slug handling capacities on the larger predicted slug
volume. Only the impact of most probable ones should be taken in account. Biggest ones should be
controlled with adapted procedures.
It should be noted frequent small slugs can also give rise to operational difficulties.
Unlike onshore or shallow water field development, deep offshore is characterised by a significant
uncertainty regarding the mud-line topography.
In order to the define the minimum stable flowrate and the effects of topography and arrival pressure,
the stability study proceeds in 3 steps:
1. Sensitivity studies to determine the effects of OLGA 2000 options (use of slug tracking according
to the flow regimes identified by the steady state study, see above). The standard OLGA dynamic
simulator can provide a preliminary estimate of riser-induced slugging. But the largest terraininduced slugs are either not predicted or underestimated.
The use of OLGA slug tracking option allows further assessment and usually extends the region of
flow instability.
2. Evaluation of the slug characteristics :lengths, frequencies, volumes or hold-ups, velocities.
3. Stability mapping and slugging severity: various slugging regions are mapped as a function of
flowrate, GOR, Water Cut, mud-line topography (up-hill or down hill) and arrival pressure as shown
on graph here-after.
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Severity index
Severe slugging
2.5
2.0
Hydrodynamic slugging
1.5
Arrival pressure
1.0
35 bara
0.5
5000
10000
Arrival Pressure
Stability Zone
25 bara
20000
RATE [ bopd]
30000
15 bara
40000
Flowrate
Note that this predictive flow stability mapping , carried out during the project phases is only indicative.
A precise quantification can only be achieved the dynamic simulation model has been tuned against insitu measurements. The actual behaviour of the flow will be very sensitive to the details of the flowline
geometrical profile and to the process control on the topside receiving facilities.
The interaction between the flow behaviour and the process regulation is an important issue that can
be investigated by coupling OLGA 2000 with a dynamic process simulator, using the OLGA server
interface. This should be contemplated only at an advanced stage of the design, once the detailed
features of the process equipment and associated regulation are specified.
The slug tracking option determines the minimum flowrate which gives total stability and the transition
region between severe slugging and stable flow with smaller slugs.
The following graph shows typical results of simulations performed to identify the flow-rate threshold at
which flow instabilities appear. Note however that this remains a theoretical approach since in actual
operating conditions, the arrival pressure would not be fixed but controlled through the process
regulation loops, allowing smooth reaction time, as is usually the case for such service. Moreover the
severe instabilities will induce some fluctuations of the back-pressure to the well bore, which in turn
may impact the productivity. In fact in the instability zone, unlike what is simulated in the case
presented on the graph, the flow boundary is not steady. Therefore some margin (tentatively 10 to 20%
on the amplitudes of the fluctuations) must be taken, when using such results as design basis for the
slug control system and for developing operating guidelines.
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8" production Flowline ; 5km long & -2% slope; BSW = 0% ; Arrival Pressure 10 bara
7000
Flow rate
(m3/d)
6000
5000
4000
Q = 2500 m3/d :
flow is stable
3000
2000
0
0
10
12
14
16
18
20
Time (hours)
Similar generic simulations can be performed for various flowline lengths, diameters or slopes as
shown in the graph here after, in which the instability region can easily be identified.
Stability in the riser
4500
4000
3500
3000
2500
6" ; 10 bar ; 0%
8" ; 10 bar ; 0%
10" ; 10 bar ; 0% BSW
2000
Stable production
1500
1000
Severe slugging
500
0
-2
-1
The graph above shows the impact on flow stability due to downward slopes just before the riser.
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To evaluate the benefits of the different concepts on a specified case, a detailed flow study from the
reservoir to the host surface production facility will return production profiles allowing for the various
production constraints.
These simulations are conducted by using a Reservoir model (ECLIPSE) and an in-house network
simulator PROII, which incorporates the TACITE Hydrodynamic flow model (Steady state two phase
mechanistic) and based on boundary conditions from the Reservoir model. This module can track the
composition of the production mixture as it actually evolves all along the flow path.
The graph below represents an example of flow study results in terms of cumulative production, and
enables us to rank the different artificial lift concepts in term of flow performances.
cumulative production evolution as a function of the activation type
NP (10^3Sm3)
2.00E+03
1.80E+03
1.60E+03
1.40E+03
riser GL
multiphase pump
eruptive
1.20E+03
1.00E+03
8.00E+02
6.00E+02
4.00E+02
2.00E+02
0.00E+00
0
1000
2000
3000
4000
date (days)
5000
6000
7000
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6.4 SOLUTIONS
SLUG MANAGEMENT
Instabilities in flow-line and riser systems are phenomena which have been addressed in investigations
or experiments for shallow water developments and still create substantial operational difficulties.
Where deepwater developments are concerned, the length and geometry of the flow-lines and risers
will cause hydrodynamic disturbances outside the usual ranges.
For such applications, the consequences in the event of severe slugging will be major problems not
only in the surface installations, but also in the wells owing to the steep pressure variations induced in
the subsea transfer lines. The use of active flow instability control systems is crucial in such contexts.
Such instabilities arise during the restart phases and under certain low flow rate conditions, and can be
aggravated by the geometry of the production sea-lines installed on the seabed, potentially leading to
riser-base induced slugging.
Different control methods can be applied, based on:
riser head choking,
gas injection at the riser base,
combined riser head choking and riser base injection,
management of incoming flow in the network,
Riser base gas lift to prevent riser induced slugging:
Gas lift has to be simulated to estimate the injection rate needed to stabilise flow.
The graph here after shows the stabilisation effect following gas-lift injection associated to choking
down at riser head.
Stabilisation with gaslift +valve closure
3
Gaslift=0 m /d
50
45
Gaslift=50000 m3/d
Gaslift=100000 m3/d
40
35
30
25
20
15
10
5
0
-5
0
50000
100000
Time [s]
150000
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On the basis of the TFE analysis of the different methods, management of flow instabilities should call
on the following methods:
Riser head choking, which limits slippage between the liquid and gas phases and
smoothes down the liquid slugs which reach the topside facilities with adverse effects
stemming from the back-pressure applied to the fluid stream,
Gas injection at the riser base which lightens the hydrostatic column, increases flowing
velocity and breaks down the liquid build-up in the lower part of the riser where the
initiation of the Slugging phenomena occurs,
Management of inflow to the subsea production line (flow-lines + riser), manifolding of
the wells onto the subsea network provides the flexibility in some cases, of shifting the
operating point in a stable flow zone, by an adequate routing of the well production.
Capability for the surface facility to handle limited liquid slugs by reducing liquid
retention time. A correct design should allow for adequate slug handling capacity in the
inlet separator acting as a slug catcher, from which the liquid drainage rate shall not
exceed the design rate of the downstream process, unless excess liquid can be
transferred to a dedicated off-spec storage tank prior to be re-circulated in the
stabilisation process. In such a case due account of gas blow-by through the
emergency drain should be taken care of in the design of the relief system, which may
become a difficult governing case.
Production well choking (bean down) to a step-back position to avoid propagation of
pressure variation into the tubing and protect down-hole sand control equipment. This
operation has to be performed in conjunction with gas injection at the riser base.
In addition to the various control methods above, prediction (real time simulation code) and detection
(sensors) means should be used to anticipate to the maximum the disrupting effects caused by the
flow instabilities and increase the possibilities of eliminating them.
Control of flow instabilities must not penalise overall well production but, on the contrary, constantly
seek the optimum in relation to the capacities of the wells and the installations.
From the analysis of the advantages and drawbacks of each method, the wise choice would appear to
be the combination of all means, so as to mitigate the shortcomings of each and obtain a consistent
overall control system.
As regards implementation and feedback, there are little or no interesting offers for command-control
software to be combined with the control system.
In this field, our in-house experience based on application of well control systems (FCW) has no
identified equivalent and its extrapolation to the control of deepwater fluxes, integrating the well, flow
lines and risers, would appear to be the essential path to follow in controlling slugging effects.
The Overall Control of Wells and Risers developed for deepwater application, executes all commands
on actuators from X-mas-tree to production and test manifold, including chemical injection treatment.
The main purpose of OCWR for oil production is to reach a maximum or target flow-rate, while:
- avoiding or limiting flow instabilities in risers and maintaining them in acceptable ranges,
- preserving the near well-bore area by avoiding substantial pressure variations,
- limiting general production shutdowns due to surface installations, by anticipation,
- avoiding hydrate formation and wax deposition in the network,
- protecting subsea equipment.
The Overall Control of Wells and Risers operates with more sophisticated external calculation tools
used as input, i.e.:
- On-line: well and riser production rate estimation calculated by Well Monitoring system,
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Off-line: assistance for decision and determination of OCWR parameters, such as network
calculation for optimal routing of wells.
OCWR ARCHITECTURE FOR LOOP ARRANGEMENT
RCHK
RISER
Mthanol
Hot Oil
P
r
o
d
u
c
t
i
o
n
T
e
s
t
GLFCV
G
a
s
GLFR
W ELL
L
i
f
t
Service
line
CHK
LinRig
e ht
Pro
d
.
The main measurements used for the wells and riser control are :
Wells and subsea manifold
Main sensors
and
calculations
Riser head
Choke downstream
pressure
Manifold Production
Pressure and Temperature
Riser choke
Gaslift flow control valve
Topside
Oil system :
Separators level
Gas system :
Separators
pressure
FPSO
temperature
Gaslift :
network pressure
compressor
intake rate
compressor
status
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Stable
Riser
stabilization
Well rate=target?
Well Monitoring
no
Stability
Branch stability ?
Wells Opening
Naturally flowing riser
start-up
Modulation
on selected risers
Bottlenecks load ?
yes
Separator system
Gas handling
Unstable
Shut-in
Load shedding
on selected risers
Production target
START-UP PHASE
PRODUCTION PHASE
Following table sum-up ways and means to reach the OCWR main principles during start-up and
production phases for oil production :
Objective
Production
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Stability
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Prevention by :
- well and riser chokes ramp
- stability
Prevention by :
- target choke
- stability
Detection :
- high riser head and bottom variations
survey
- too low riser head and bottom pressure
survey
- backflow risks survey
- sand detector survey
Detection :
- too low riser head and bottom pressure
survey
- backflow risks survey
- sand detector survey
Action
- choke ramp suspension
- well choke beaned
Anti-hydrates
Action
- alarm
- well choke beaned
Prevention :
Prevention :
- routing of wells according to minimum - continuous methanol injection
flowrate per line
- riser head temperature survey and
- automatic injection of methanol before
automatic injection of MeOH if required
well opening
-
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Due to eruptivity limitation, flow enhancement can be applied at different locations by providing
mechanical energy or lightening the produced fluid:
In the wells by gas-lift or pumping (ESP)
in the riser by gas-lift
at the mud-line near the wellheads or near the riser base by
using multiphase pumps or a water separation system.
Artificial lift in the wells
For deep-water applications, possible artificial lift systems include down-hole equipment. All the
techniques for boosting energy in deepwater subsea wells have to contend with the major constraint of
keeping risky and costly intervention to a minimum. Our experience of wells gas-lifted and especially of
lift with ESP has shown that these techniques need intervention in the wells for maintenance or repair
of down-hole components.
The complexity of down-hole equipment limits its reliability and entails costly well intervention and
associated production losses. This option is to be evaluated, but only for wellhead platforms (dry tree
architecture), mainly due to intervention consequences in subsea condition.
Gas lift at riser base
High pressure gas from (export or re-injection network) the compressors is injected at the riser base
and enhances flow making use of a well known artificial lift technique used to improve well
performance with low associated CAPEX.
The efficiency of riser gas-lift increases with the water depth and takes advantage of riser height.
Dedicated studies provide riser base flowing pressure versus liquid rates for different ratios of injected
gas (VLP curves) and for different water cuts.
The results of simulations enable an appropriate GLRi to be chosen, providing a nominal gas-lift flow
rate per riser for the design conditions.
P re ssure e volution @ rise r ba se
140
Riser basePressure(bar)
120
100
WLR %
80
0
60
80
60
40
20
0
0
500
Inje cte d Gas
1000
KSm 3/j
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Special attention must be paid to erosion due to gas expansion causing high velocity in the upper part
of the riser (refer 6.3.1).
In addition, before any need for continuous lift, the kick off phase during the re-start phase can be
handled easily by gas-lift. Gas injection can also be used when low flow conditions prevail to control or
prevent slugging phenomena in the risers. This technique can be advantageously combined with other
emerging subsea techniques such as multiphase pumping (Topacio development) or water separation
(Troll C development).
Gas-Lift is a reliable lift technique to use in deepwater condition because it needs very simple and
reliable static subsea equipment.
Subsea multiphase pumping
Multiphase pumping is installed on the seabed where it accelerates oil production from the outset
(maximise draw-down when associated with gas-lift), and can shorten the recovery time considerably.
For satellite development, this technique can extend the step-out distance to existing infrastructures,
provided that the temperature preservation of produced fluids is not a bottleneck (see 7 Thermal
management)
To cope with the expected range of total flow produced by the wells, flexibility can be provided by a
modular arrangement of 2 or more pumps in parallel. In addition, this configuration minimises
maintenance weight for the pump unit and, in the event of failure of one pump, the other(s) can reliably
stand in to maintain sufficient flow.
A multiphase pump arrangement module is a balanced choice between:
Flow energy needs related to rising hydrostatic pressure brought about by increased watercut, and the consequent reduction in the gas volume fraction,
Flexibility to handle variations in gas content,
Technical limitations related to high power demand and its distribution,
Required level of redundancy and reliability to satisfy,
Maintenance criteria and associated limitations due to intervention vessel availability and
performances.
Installation of multiphase pumps at the mud line offers many advantages such as limited gas volume
fraction (better efficiency of multiphase pump) or early energy addition to the evacuation system. But
integration in a deepwater environment requires a qualification process for such components as
electric motor (RPM, sealing, cooling, power demand) or power distribution (umbilical, frequency
converter, transformer, wetmateable connector).
The reliability of such technique is a key point in responding to deepwater application challenges.
Topacio field in Equatorial Guinea (Exxon-Mobil) application (2 x 1,1 Mw pump units). The
multiphase pumping units use the helico-axial technology and are driven by electrical motor 1Mw @
5000 rpm wxith an expected differential pressure of 35 bar. The pump and the motor are retrievable
according to a cartridge design. The tie-back distance is 8,5 kilometres to Zafiro host facility. This
application should give us the maturity of such technique in 500 meters water depth. Pump module
was installed in august 2000. To date this implementation is the only subsea application of the
multiphase pumping technology.
Subsea Separation (emerging technology)
Subsea separation should consider two alternatives: water / hydrocarbons separation and gas/ liquid
separation to be deployed either near the wellheads or at the riser base.
Subsea water separation would prevent the increase of the hydrostatic pressure stemming from watercut evolution, and lower the liquid volume to transport through the sub-sea line pipe.
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The first application in subsea water separation has been performed by Norsk Hydro. A unit has been
installed by 350 meters water depth at Troll C field The pilot operates as a separator and re-injection
station for 8 wells with a capacity of 10 000 m3/day. For water re-injection the solution consists in a
variable speed water pump (2 Mw) with injection rate 6000 m3/day. The unit was started in may 2000
with an early failure on the electrical wet meteable connector (MECON connector). After retrieving the
th
electrical motor, the connector was repaired and the unit was restarted the 25 of august 2001.
For gas dominated systems: Gas-liquid separation allows under certain condition a better valorisation
of the gas, it will also help the gas transfer over huge distance.
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Thermal Management
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7. THERMAL MANAGEMENT
Note : This theme is closely integrated with the Hydrodynamic theme as both use common simulation
tools and flow and thermal parameters interact with each other
Flowing conditions, common to all solutions (passive or active) as heating should be minimised
while producing,
Shutdown conditions for which the requirements differ according to the selected solution with
respect to actual risk of solid deposition.
The thermal requirements for both flowing and shutdown conditions are specified for various cases
intended to cover nominal and transient modes likely to be anticipated during field life.
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7.3 METHODOLOGY
THERMAL BEHAVIOUR: INSULATION REQUIREMENTS
Thermal calculations are performed, at the parametric stage of study with the purpose of assessing the
overall thermal insulation requirement (U-value), with PROII/US14 simulator in steady state flowing
conditions and with OLGA to investigate the shut-down and restart conditions. In case of thermal study
sub-contracted to a Service or Engineering company, or in case of study covering both normal flowing
conditions and shut-down conditions, OLGA shall be used throughout. Temperature drops are mainly
due to heat exchanges with the cold sea-water and, and to Joule Thomson effect due to gas expansion
mainly in the riser section.
The aim of these calculation is to determine the required Overall Heat Transfer Coefficient (U value)
for the different parts of the production network ( well tubing, flowline and riser ) in order to ensure a
minimal arrival temperature, and an adequate cooldown delay to avoid hydrates risk in shut-down
conditions.
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This thermal evaluation has to take into account heat exchange arising from conduction, free
convection and possible active heating device (electrical or fluid transfer). ). The understanding and
modelling of the thermal transfers in deepwater architectures are generally more complex than for
shallow water or onshore applications, due to the non-cylindrical/non-symmetrical geometry of the
systems such as bundles or other complex insulation concepts. Therefore the use of CFD tools like
FLUENT or CFX may be required to calculate U values.
40
35
30
6"
8"
6"
8"
25
20
15
10
5
Insulation : 50 m m of polyurethane (
=0.11
W / C)
0
0
500
1000
1500
2000
liquid flow rate (m 3/d)
2500
3000
3500
4000
L=5km
L=5km
L=10km
L=10km
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Similar simulations can be performed for various insulation levels with a given geometry as shown in
the following graph.
40
U=2.5
38
U=2
U=1.5
U=1
36
U=0.5
34
32
30
1000
2000
3000
4000
5000
6000
7000
8000
9000
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Case : 5 km x 8" flowline ; 2000 m3/d ; Wellhead temp. = 48C ; BSW = 0 ; 10 bar on FPSO
Time after shut down before 20C is reached
45
40
35
Time (hours)
30
well Head
mid flow line
bottom of riser
mid of riser (gas)
25
20
15
10
0
0
Sensitivity studies
In order to better analyse the previous results, various sensitivity studies are carried out:
Line Geometry according to different Slope value, and including dips and bumps as relevant.
Closure sequences between well valves and surface choke with associated depressurisation,
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7.4 SOLUTIONS
To improve thermal performances during the cool-down associated with shutdown phase, three means
can be applied:
1. Limit heat exchange (losses) with good insulation (low U values)
2. Heat the lines (electrical or hot fluid transfer by circulation).
3. Increase the thermal capacitance of the system (higher m.Cp values)
The state of the art thermal management solutions can be divided into two categories, passive
insulation and active heating.
In passive insulation, the industry has advanced traditional materials such as syntactic foams for
application in water depth up to 3000 m. Some new insulation concepts are vacuum insulated pipe,
jacketed insulation with microporous insulation with or without vacuum, aerogel beads, and area
gel vacuum panels. A new concept of Phase Change Material is developed, which uses latent heat
to extend the cooldown time.
In active heating, current methods include hot fluid heating and electrical heating. Hot fluid
heating is the most reliable option and may be also more economical. Drawbacks are the
temperature limit, ,non-uniform heating along the flowline, and large Electrical heating includes
SECT heating, low power electrical heat traced, and direct electrical heating. The first two are
under development. The direct heating methods have been used for 2-3 fields, with apparent
successes. Electrically heated systems have issues of voltage, reliability of electrical connections,
interference, corrosion, and possibility of broken electrical cables.
Thermal tests
Full-scale thermal tests can be expensive, but is necessary to ensure the performance of the installed
flowline system is as designed. The expense of thermal tests is also very small when compared with
the remediation (pigging issues or hydrate removal) cost due to insulation failure.
Thorough thermal tests should be performed on new thermal management (insulation, active heating
etc) concepts, to prove the concepts and to develop proper analytical tools for use in design.
For actively heated systems have many more issues to cover than tests of passive insulation systems,
due to the addition of system function and components.
Natural convection in insulation is the major cause of many past insulation problems. For open-cell
polyurethane foams under pressure, the pre-cast insulation allows significant natural convection to
occur and degrade the thermal performance by a very large extent. Similar problems are expected in
insulation with porous and permeable insulation such as fiber glass and rockwool, if high pressure is
applied.
For wet insulation system such as external syntactic foam insulation, pre-cast modules result in gaps in
insulation and between insulation and flowline/riser. Strong natural convection effect was observed in
thermal tests.
One method to minimize the natural convection effect is to cast the insulation material in place. For
syntactic foams, this eliminates the natural convection in the insulation. For pressurized open-cell
polyurethane foams, there are still natural convection in the cells, but the effect on OHTC is 20% or
less.
There are two types of thermal management solutions: passive insulation and active heating. This
section reviews the state-of-the-art thermal management solutions of both types, particularly in issues
related to testing of these solutions. The solutions will be discussed in the context of offshore
developments.
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applications, the pipe-in-pipe annulus where the panels are applied can be vacuumed to a moderate
level.
Thermal Tests
The issues in thermal tests of these insulation systems are the same as those of OCPUF insulated
systems, except that the influence of vacuum levels needs to be determined by the tests.
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the fluids. This philosophy is based on the observation that, due to the short resident time of produced
fluids in the riser during normal production, heating in the riser to raise the fluid temperature is usually
not effective.
Thermal Tests
Thermal test of actively heated flowlines should cover a much wider scope than passive insulation,
because of the added system component and function.
First, thermal performance without heating needs to be determined. The issues and methods are the
similar to passively insulated flowlines. The steady state test methods are directly applicable. But
cooldown tests with lumped thermal mass data reduction method cannot be directly applied because of
the presence of heating pipe and the heating fluid, both having substantial thermal mass. To use the
cooldown tests, a new data reduction methodology must be developed.
Second, heating performance needs to be determined. The heat transfer rates between the heating
fluid and the produced fluid, at various heating flowrate and heated fluid properties (and velocities if
continuous heating), are a key factor determining the heating performance. However this is one of
most uncertain areas in prediction and design.
Thermal tests need to be carefully performed so that the system performance can be assured for the
expected ranges of operating conditions. These tests should also provide data for improving prediction
tools for future designs.
Another aspect of the heating performance is the heating efficiency, i.e., how much of the heat lost
from the heating fluid is used to heat up the fluid and how much is used to heat up the insulation or lost
to the ambient.
Hot water heated flowline systems frequently have spacers or other components that can degrade the
insulation or heating performance. These should be included in the analysis and determination by
thermal tests.
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of the flowline. If large differences exist, the lumped thermal mass data reduction method cannot be
used.
Heating performances also need to be determined. SECT heating tubes are welded on to the flowline
and thus the heat resistance is expected to be small. However the relationship between the heating
output and the heat gained by the produced fluid needs to be determined for a range of heating rate,
flow velocities, and fluid properties. This determines the heating power requirement, fluid warm-up
time, as well as heating efficiency of the system.
Due to the localized nature of the heating tubes, the temperature at the tubes can be quite high. The
thermal test should determine the temperature during various operating conditions. This helps
determine whether the insulation material has sufficiently high temperature rating, and whether
potential problems exist in accelerated aging of the insulation materials due to the higher temperature.
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seawater (in parallel). Only AC current can be used because DC current in seawater will cause
corrosion on all nearly structures. In a closed loop system uses a separate cable or the steel jacket
pipe (if present) as the return conductor. Both AC and DC currents can be used in closed systems.
While the DEH concept has a much longer history in the industry, only recently have field tests and
installations been done:
DeepStar IV engineering study and full scale field demonstration. This tests driven by Shell (Ron
Bass) were performed in Norway and operated by Alcatel Norge with the support of Thermotite
(electrical & thermal insulation). Reports are available.
Statoil Sleipner (North Sea WD: ? installation 1996) used induction system on a single pipe 20
12.6 Km long for temperature maintenance.
Statoil Asgard (North Sea WD: 400m installation 2000) used DEH for the first time. Open loop
systems were used on a total of six flowlines 8. The Heating cable lengths were 6 & 8.5 km long.
The maximum system voltage required was 5.3 KV and the maximum system current was 1520 A,
which occurred in the case of heating from complete cooldown state. The system was designed for
hydrate prevention, and was only to be used during shutdown or warm-up (maintenance at 27C).
70 80 watts/m of heat is lost to the surroundings. Heating requires a supply of about 105 W/m.
Statoil Huldra (North Sea WD: 400m installation 2001) development. Open loop system was to
be used on the 16 km x 8 condensate pipeline. The system DEH will be used similarly as Statoil
Asgard except for it also will be used for wax prevention and removal, and should be used
continuously during the last four years of field life.
Shell Serrano/Oregano (GOM WD: 1000m installation 2001) subsea developments (Gulf of
Mexico). The development used 6 in 10 pipe-in-pipe insulation and closed system DEH Mid line
active heating to tieback the two fields to Auger TLP, with distances about 6 miles (10 km) and 7.5
miles (12 km) respectively. At the platform end, the power supply is connected to the inner pipe in
an electric isolation joint. At the steel bulkhead at the PLEM, the two pipes are connected so the
AC electrical current can flow back to the platform through the outer pipe. Due to skin effect, the
current is concentrated within a thin layer at the OD of the inner pipe, and a thin layer at the ID of
the outer pipe. Through tests Shell proved that electrical leakage to seawater is negligible due to
this phenomenon.
As mentioned in HYDRATES theme ( 2.4.4) Shell plan to use (installation in 2003) Direct
Electrical Heating system for hydrate remediation (back-up solution) on Nakika field (WD:
1900m) on the different flowlines (10 x 16 PIP length 2 to 12.8 Km).
The most challenging issue in design was the possible effects on corrosion and signal interference
from impressing high-voltage AC over DC cathodic protection.
However details of the solution are not available. Short circuit is a major risk aspect in the system. In
installation, water egress in the pipeline must be strictly avoided and every joint of pipe was tested
before the next was installed.
In the current configuration, the DEH method is limited to 15 miles due to annulus material breakdown
issues. Increasing to 30 miles can be done but involves subsea isolation joint and electrical connection.
Due to high electrical impedance of flowlines, DEH methods have a common shortcoming of high
voltage, possibly close to 0.5-1 V/m.
Thermal Tests
For the DEH systems, the tests for thermal performances of the insulation while no heating is applied
are the same as those for passive insulation system. There are no additional cable or heating pipe.
The steady state and cooldown test methods can be used in the same way.
As with other actively heated systems, heating performances should be determined, in all of the
designed operation modes such as warming-up before production begins,
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temperature keeping during production shutdown, or continuous heating during normal production.
Direct heating is expected to be efficient since the heating surface is in contact with the fluid. The
heating performances to determine are the power requirement in the designed operations at the design
criteria. The expected range of fluid properties should be covered. The temperature of the flowline is
expected to be close to that of the fluid during heating, but measurement should be made to confirm.
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Directional
Coupler
Raman
Scattering
Laser
Source
Brillouin
Brillouin
Anti-Stokes
Signal
Raman
Band
Processing
Stokes
Raman Band
Wavelength
SENSA is the leader company for DTS using Raman spectroscopy (Reflection Raleigh + Stokes &
anti-Stokes). Temperature limitation is around 150C, the maximum length is:
< 10 kilometres with temperature (+/- 0.5C) measurement every metre using multimode fibre.
10 to 12 kilometres with temperature (+/- 0.5C) measurement every 2 metres
using multi-mode fibre.
< 30 kilometres with temperature (+/- 1C) measurement every 10 metres to 30
metres using mono-mode fibre.
There is a limitation with the number of measurements (< 10 000 points) per fibre, and the sampling
time is around 15 minutes.
To date SENSA claims 130 DTS application. Among them we can mention: Gulfaks (2 DTS deployed
on 15 Km by Statoil), Wytch Farm (DTS on 11 Km by BP), Tern & Bellridge (Shell), Coalinga (well
temperature monitoring on steam flooding Chevron California), Marlim (monitoring of well temperature
following collapse problem with production casing on a wellhead platform, BP)
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Passive insulation system allowing enough time to apply preservation procedures. During this
period, the produced fluids in the subsea production system are replaced by pumping storage oil
Active insulation system by heating the subsea lines to compensate for thermal losses during
shutdown in order to maintain line temperature outside the hydrate region, or re-heat fluids prior to
production restart (see Hydrate Theme 2).
Other areas:
Valve location can be a problem due to water or gas accumulation, in order not to foster hydrate
blockage during closing / opening phases.
For a non-heated system (or one in which only the riser will be heated), the lines must allow
access by coiled tubing at any point in the subsea system. This will be useful for removal in the
event of hydrate blockage. The CTU (coiled tubing unit) located on the surface utilities allows
circulation of inhibitors or/and storage oil necessary to restore fluid circulation,
All weak points in terms of thermal insulation, mainly connectors, must be placed at high points in
the system where gas pockets may form after a shutdown. This will allow water to drain down to a
warmer location,
Instrumentation points, such as temperature and pressure transmitters, must be non intrusive, and
placed on the upper third of the pipe, as near as practical to the 12 oclock position,
Dead legs namely: piping of the pigging module, piping downstream of the dispatching valves (subheaders), piping between header isolation valves and sub-headers must be minimised. Their
shapes must also be such as to avoid water accumulation,
Gas-lift line geometry, if non-heated, must allow water drainage within the production line. As liquid
may enter these lines on shutdowns, their shape must allow the water to drain out of them by
gravity so as to minimise the hydrate formation risk.
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Erosion / Corrosion
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8. Erosion / Corrosion
8.1 Terminology
The term "erosion-corrosion" word is a very general one, incorporating a very wide range of
phenomena, from erosion-induced degradation (i.e. with almost no corrosion effect) to corrosion
degradation aggravated by increased ionic diffusion (i.e. without any mechanical effect).
For reasons of clarity, 2 basic considerations and 4 distinct terms will be used:
Basic considerations:
1. The term "Erosion" will always refer to mechanical effects, produced by either liquid or solids,
and either on the metal itself or on protective layers formed on the metal,
2. The term "Corrosion" will always be used when the final degradation is brought about by the
electrochemical reactions involved in corrosion phenomena.
Terms used:
1. "Erosion" (Er): Degradation resulting exclusively from a mechanical effect of the fluid on the
metal itself, without requiring any corrosion reaction (e.g. sand erosion in dry gas or in oil
containing no water). Both "solid erosion" and "liquid erosion" could be used, but in practice liquid
erosion phenomena (without any solid or any corrosive liquid) are not of any real concern in oil and
gas production applications.
2. "Solid erosion-corrosion" (S E-C): Final degradation results from corrosion reactions, but solid
particles contribute to the mechanical removal of a protective layer such as a passive film or an
oxide - carbonate sulphide protective layer.
3. "Liquid erosion-corrosion" (L E-C): Final degradation results from corrosion reactions, but liquid
flow contributes to the mechanical removal of a protective layer (by fatigue cracking, shear stress
effect). No solid particles involved.
4. "Flow-enhanced corrosion" (F-E C): Flow effect is exclusively chemical and electrochemical,
without any mechanical effect (flow only enhancing diffusion of species which favour
electrochemical reactions and/or dissolution of the protective layer). No solid particles involved.
The overall term of "erosion-corrosion" is thus only used as a general one. It currently incorporate only
the 3 first phenomena (no mechanical effect of flow velocity in F-E C). However, in practice, it is
difficult to draw any clear distinction between F-E C and S E-C (corrosion layer removal frequently
resulting from a combination of mechanical and chemical effects which can hardly be distinguished).
As a consequence, although F-E C is no longer mentioned, it is currently covered by limits used for
L E-C.
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Material
Possible erosion-corrosion
phenomena
Key factors
Carbon steel
All
Er and S E-C
Er
Equipment
Usual materials
Possible erosion-corrosion
phenomena
Screens
Stainless steels
Erosion
Carbon steel
Hard materials
Erosion
Stainless steels
Erosion
Carbon steels
All
Top of risers
Stainless steels
Carbon steels
All
Stainless steels
Carbon steels
All
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Erosion-corrosion
phenomena involved
Material involved
Carbon steel
Carbon steel
Solid particles
Inhibitor
Carbon steels
Based on these considerations, the main issues of a deepwater development regarding erosioncorrosion management are to:
Assess all possible erosion-corrosion risks throughout the expected lifetime of the installations,
and define practical limits for the occurrence of such risks (flow velocity limitations, particle size
limitations, allowable sand flow rates)
Define an overall material selection/corrosion management policy adapted to the effective erosioncorrosion risks, by the optimum combination of an adequate design (sufficient diameter, avoidance
of irregular geometry), the use of corrosion-resistant alloys, a consistent flow management, the
application of corrosion inhibitors
Implement monitoring tools, methods, programmes and evaluation criteria aimed at verifying the
successful application of the above corrosion management policy.
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Type
Evaluation
concerned
Usefulness
Expected lifetime
All
L&S EC
Er.
Reservoir
P: 20%, T 5 C
Production data
Flow rate of each phase on all
evaluation points (or equivalent data
such as Oil flow rate + GOR + BSW)
All
All
P: 20%, T 5 C
S EC, Er
All
Internal diameters
All
Specific profiles
S E-C and Er
L & S E-C
L & S E-C
Geometrical data:
Produced water:
Detailed water analysis
Produced gas :
2
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L & S EC
Viscosity
Er
Er
S EC, Er
Average diameter
S EC, Er
Granulometric profile
S EC, Er
Solid particles:
Very useful
* : Usefulness: R = Required (for risk assessment), U = Useful, but not mandatory. The evaluation may
be less precise if the data is not available, but without any critical impact in most cases.
8.4 Methodologies
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A difficult and very specific matter, for which there are not as yet any general criteria available.
To be analysed on a case-by-case basis, if this lack of water is considered likely to last any significant
time.
The most common equation for calculating flow velocities is the API RP 14 equation:
Vcr = C / ,
Where C is a constant and is the average density of the fluid considered.
This equation is currently used by process people in terms of V limiting values (e.g. a C value < 100
2
in US units is almost equivalent to a V < 15000 in SI units)
2
Although this simple equation is not fully acknowledged to cover the wide variety of effects and
parameters involved in critical velocity determination, it is recognised as a quite valid design and
engineering criterion, as long as constant values (C parameters) are adjusted to the type of
media and service conditions.
As an example, C values in the range of 100 to 250-300 are indicated in the literature for different types
of fluids (gas, oil, water, mixture of these 3 phases), different materials, presence of corrosion
inhibitors
An internal procedure indicating C values (or limiting velocities in m/s) for different production cases is
included in the in-house document Technical Corrosion Practices. These values are to be used for
design and engineering purposes.
If the case under evaluation is not included in this procedure, or if higher values than the reference
limiting ones are calculated, corrosion specialists must be contacted to conduct an in-depth evaluation
(including not only flow velocity but also flow regime, duration of high flow conditions, combination of
favourable and adverse parameters). The in-depth evaluation is then based on more detailed criteria
included in the in house LIPUCOR calculation tool.
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the increased difficulty (more influencing parameters, in particular solid flow rate, particle size and
shape, fluid composition),
less field experience (solid particle production being almost systematically prevented, it is only
experienced following accidental failure of sand prevention methods)
The practical difficulty of distinguishing the pure Erosion effect (direct metal removal) from the
Solid Erosion-Corrosion effect on failed equipment.
8.4.1.3 Erosion
The risk of erosion damage is of particular concern for deepwater developments since most of the
reservoirs are unconsolidated ones, i.e. massive sand production may occur if no bottomhole
prevention is applied, or if it fails. In addition, high flow velocities are expected and flow limitation,
because of sand presence, is of course a costly method when significant production loss is involved.
As opposed to L and S E-C, erosion damage no longer involves any electrochemical corrosion
phenomenon. Consequently, neither water presence nor corrosive behaviour is necessary for erosion
damage, although combined or even synergic effects between erosion and corrosion damage may
occur in practice.
Erosion prediction models are based on a simple Erosion Rate prediction equation as follows:
n
ER = k * M * V / d where:
M is the mass flow rate of sand production (in g/s or kg/d...)
V is the mixed flow velocity of the fluid, i.e. the sum of liquid and gas superficial flow velocities in 2
or 3 flow (m/s)
d is the pipe ID (mm or m or ")
k is a constant.
n value is given in the range of 1.7 to 2.5, depending on the models used.
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The M parameter may also be replaced by the mass sand concentration parameter (usually in ppm).
n+1
When the latter is used, the ER is then proportional to V , i.e. to an exponent of about 3 on the
velocity (M being proportional to both the sand concentration and the fluid flow rate, hence the fluid
velocity).
st
There are various models available based on this 1 equation, and which have been improved and
adapted to different types of fluids (k constant being dependent on a large number of parameters). In
particular, initial models were dedicated to gas fluids (with almost no liquid), and then to liquid fluids,
whereas present models combine the 2 previous approaches for application to 3-phase flowing
conditions (Oil + gas + water).
The most adequate models for preliminary evaluation are:
1. Salama-Venkatesh 1983, for gas applications, with almost no liquid (typically gas-condensate
fluids),
2. Salama 1998 (OTC papers nos. 8898 and 8900) for liquid and 3-phase applications.
More complex models (Tulsa, DnV, AEA) exist but their limits of application are not yet fully known
(to be evaluated in 2001-2002). They should therefore only be used on a case-by-case basis.
These models are designed for calculating Erosion Rates ER (in mm/yr) versus sand production, flow
velocity and other contributing factors (the more complex the model, the higher the number of
parameters included). As a consequence, limiting flow velocities can be evaluated for a specified max.
Erosion rate.
The following qualitative considerations must also be taken into account:
Even though vendors claim their prediction models are accurate, the effective accuracy of the
predicted values must still be considered as quite low. In particular, whatever the accuracy of the
model itself, the data used for calculation are generally not very accurately known. In particular,
how can the simultaneous evolution over time of pressure, BSW, flow rate, sand production rate
and particle size distribution be accurately predicted? It is thus recommended to use these results
mainly in 3 wide categories, e.g. low risk when ER< 0.1 or 0.05 mm/yr, high risk when ER> 1 or 2
mm/yr, and medium risk between these 2 extreme cases.
As long as bottomhole sand prevention is implemented (with screens and gravel-packs), two
distinct cases of sand production must be separately considered: normal residual sand production
through gravel-pack and screens (with a very low amount of sand produced and a low particle size
of 10 to 30 microns) and accidental massive sand production, up to the max. particle size of the
reservoir, in case of accidental or progressive gravel-pack/screen damage.
For oil production, i.e. with a significant amount of liquid produced, erosion risk is almost negligible
under the usual flow velocities (15 to 30 m/s) as long as particle size is below 50 microns. The
normal residual sand production through undamaged screens consequently has no significant
impact on erosion risks.
Erosion damage, hence erosion prediction models, first concern particular geometries where sand
particles preferentially impact the pipe wall. As a consequence, chokes, short radius elbows, Tees,
restrictions are particularly concerned, whereas erosion along straight lines (either horizontal or
vertical) is very rare.
The 2 more critical areas where erosion risks merit consideration are usually:
The subsea flow-line, downstream of the choke, because of the sudden pressure loss at
the choke level, the relatively low diameter and the irregular geometry of the flowline,
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The top of riser, because of the lower pressure level and higher gas content than at higher
pressure.
At present, there is no adequate predictive erosion model for chokes, i.e. for the most severe
erosion conditions of all production equipment (very high flow velocities, highly irregular
geometrical profile, specific materials).
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1000
100
10
0
5000
10000
15000
20000
25000
30000
35000
40000
45000
50000
Prevention method
E-C phenomena
concerned
Comments
Material selection
L and S E-C
Well design
S E-C and Er
Flowline/ Piping
design
General design of
Minimizing geometrical
All
TotalFinalElf E&P
DGEP/SCR/RD/UGF
Ref. : UGF/2001-135
Rev. : 0 01 / 2002
anomalies/irregularities
uniformity of internal
diameters
Produced fluids
L and S E-C
Production
management
S E-C and Er
Production
management
All
Production
management
All
Almost all the methods mentioned above must usually be implemented within a complete project on
the various components of the production circuits from bottomhole to the top of the risers.
TotalFinalElf E&P
DGEP/SCR/RD/UGF
Ref. : UGF/2001-135
Rev. : 0 01 / 2002
As for L E-R, the 1 key point is the location of the tools, which must be placed in the most critical
areas. These need to be precisely defined and checked later during the Engineering phases of the
Project, when the geometry of the equipment is known.
In addition, as none of these monitoring solutions is fully reliable or fully indicative of all possible
erosion effects, a combination of several methods is necessary.
Methodology
Main advantages
Acoustic sand
detection
To be located on an
appropriate area, where
particle impacts are effective.
Solid content
measurement on
liquid samples
Choke performance
monitoring
Easiness
No specific equipment
required (only data
management)
Methodology
Main advantages
Stainless steel ER
probe
Intrusive probe.
Field Signature
Monitoring
Expensive, particularly in
deepsea applications
Monitoring of a significant
portion of pipe (0.2 to 1 m) of
any size and shape (straight
TotalFinalElf E&P
DGEP/SCR/RD/UGF
Ref. : UGF/2001-135
Rev. : 0 01 / 2002
Instrumented
ultrasonic wall
thickness
measurement
Instrumented periodic US
monitoring probes, with
several probes for covering a
significant area
Non-intrusive
Sacrificial piping
element
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Well Metering
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9. WELL METERING
The financial requirements and technical constraints require development schemes in which several
wells produce through a single flowline. Obviously, these same reasons prevent the use of a dedicated
production metering flowline. Consequently, any metering method envisaged is more complex and
costly than usual (e.g. production loss, high methanol consumption, etc.) and the risk of failure or
incidents is increased.
From a technical aspect, several potential solutions can be implemented using:
A test separator,
Multiphase meters,
Flowrate calculation tools based on flow modelling,
A combination of these techniques.
9.2 SOLUTIONS
1. Direct testing through a surface test separator.
In this case, testing the well requires either shutting-in the other wells connected to the same flowline
or switching them to another available flowline, if field architecture permits (loop layout). The main
disadvantages include significant production losses, huge consumption of methanol to inhibit the
resulting dead branches, gas-lift to stabilise flow or a number of subsea valve operations. The main
advantage of this approach resides in its precision, which is the same as the separator metering
methods usually available . Moreover, this method is not affected by failures in subsea gauges.
An alternative to direct well testing through the separator is to test n linear combinations of n wells.
This methodology is called permutation. In practice, it is very difficult or even impossible to apply
when the number of wells per branch exceeds 3.
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