ECE 5.4 Help
ECE 5.4 Help
i: Discount rate
MSS
11.5-
13Cr 0.15 - - -
13.5
S-13Cr
10.5- 0.012 1.30
(various 0.015 1.5-7.0 0-3.0 Cu
13.5 max. max.
ranges)
22CrDSS
25CrDSS
Cu 0.20-
24.0- 5.50- 2.50- 0.10- 1.0 0.80
S31260 0.030
26.0 7.50 3.50 0.30 max. W 0.10-
0.50
Cu 0.5-
24.0- 3.0- 0.20- 1.0 1.0
S32760 0.030 6.0-8.0
26.0 4.0 0.30 max. W 0.5-
1.0
Cu 0.20-
24.0- 2.50- 0.24- 1.0 0.80
S39274 0.030 6.0-8.0
26.0 3.50 0.32 max. W 1.5-
2.5
Nickel-Base Alloys
Cu 1
Alloy 20- 1 max.
0.02 50-52 9-11 -
2050 22 max. W1
max.
N06985 Fe 19.5
22 44 7.0
(G3) Cu 2.0
N06950 Fe 17
20 50 9
(G50) W 0.7
Fe4-7
N10276 14.5- 1 C0 2.5
0.02 Balance 15-17 -
(C276) 16 max. W 3.0-
4.5
* The composition given for the martensitic stainless steels
(MSS) is very broad as there is a wide range of
compositions available from different manufacturers.
MSS - Standard 13Cr
The MSS - Standard 13Cr martensitic steel (typically AISI
410 or 420) has been widely applied in sweet wells
internationally.
All Graphs: Graphs for pH, water flow rate, water cut,
liquid hold up, liquid velocity, gas velocity, glycol
concentration, temperature, pressure, corrosion rate &
flow regime, and heat transfer factors; all versus
distance along the pipeline.
Details: Additional information including velocities,
composition data, expected flow pattern and sour
service requirements.
Project
The Project tab of the Flowline Corrosion Predictor is used to
input Project information into the Flowline Corrosion
Predictor.
MSS
22CrDSS
25CrDSS
Cu 0.20-
24.0- 5.50- 2.50- 0.10- 1.0 0.80
S31260 0.030
26.0 7.50 3.50 0.30 max. W 0.10-
0.50
Cu 0.20-
24.0- 2.50- 0.24- 1.0 0.80
S39274 0.030> 6.0-8.0
26.0 3.50 0.32 max. W 1.5-
2.5
N08904 19- 2
0.02 23-28 4-5 -
(904L) 23 max.
Fe 5
max.
N06625 20- 0.5 Ti 0.4
0.01 Balance 8-10 -
(625) 23 max. max.
Nb 3.15-
4.15
i: Discount rate
n: year of the event
Bulk Calculation
Bulk Calculation is used to load multiple flowline values for
calculation into ECE.
Factors (1) and (2) can slightly increase the corrosion rate
under certain conditions, but, except at very low
concentrations of H2S, these effects are usually outweighed
by significant reductions in corrosion rate due to sulphide
scaling, factor (3).
The protectiveness of the sulphide layer is expressed in the
form of a multiplier on the CO2 corrosion rate:
Reference:
Michel Bonis (TOTAL E&P), Weight-loss corrosion with H2S: From facts to leading
parameters and mechanisms, NACE Corrosion 2009, Paper 09654.
Stephen N. Smith, Michael W. Joosten, Corrosion of Carbon Steel by H2S in CO2
- containing Oilfield Environments, NACE Corrosion 2006 Paper 06115.
pH and Water Chemistry
The pH is evaluated by calculating the concentration of the
following species:
CO2, H2CO3, HCO3-, CO3--, H2S, HS-, S--, H+, OH-, H2O,
Fe++ , CH3COOH (acetic acid), CH3COO-.
The effective carbonic acid concentration is calculated from
the CO2 fugacity and Henry's constant, which is
temperature dependent. The concentrations of the
carbonate and bicarbonate species then follow from the
dissociation constants, which are also temperature
dependent. For the H2S derived species the calculations are
analogous.
The pH is finally obtained by changing the H+ concentration
until all ionic species are in equilibrium of charge.
An important role is played by dissolved iron bicarbonate,
which is the initial corrosion product formed. Although the
solubility of FeCO3 is quite low, the slow reaction:
Fe(HCO3)2 ---------> FeCO3 +H2CO3
causes a supersaturation with dissolved Fe++, which
increases the pH (=pHact) and reduces the corrosion rate.
The extent of supersaturation with Fe(HCO3)2 is
temperature dependent (more supersaturation at lower
temperature). The precipitation rate of FeCO3 (=removal
rate of Fe(HCO3)2 from solution) can be calculated from
van Hunnik's formula:
Reference:
C. de Waard, U. Lotz and A. Dugstad, Influence of Liquid Velocity on CO2
Corrosion: a Semi-Empirical Model, NACE Corrosion 1995 Paper 128.
E.W.J. van Hunnik et al, The formation of protective FeCO3 corrosion product
layers in CO2 corrosion, NACE Corrosion 1996, Paper 6.
Fang et al, High salt concentration effects on CO2 corrosion and H2S corrosion,
NACE Corrosion 2010, Paper 10276.
L. Smith, C de Waard, Corrosion Prediction and Materials Selection for Oil and
Gas Producing Environments, NACE Corrosion 2005, Paper 05648.
R. Enick, S Klara, CO2 solubility in water and brine under reservoir conditions,
Chem Eng Comm 1990, Volume 90 pp 23-3.
Influence of Crude Oil
The presence of hydrocarbons may have an important effect
on corrosion rate. At higher velocities, the water may be
entrained in the oil, and the effect on corrosion than
depends on how well the water can wet the steel's surface.
The ECE model proposes that this wetting ability depends on
the amount of water which the oil can carry in the form of an
emulsion. The ability of an oil to form emulsions with water
can be expressed as the emulsion breakpoint, which is the
amount of water above which the emulsion will separate.
Water contents less than this breakpoint will cause less
water wetting of the steel, and give less corrosion since the
water is being carried as an emulsion in the oil. The
corrosion rate reduces as the water content reduces. Water
contents greater than the breakpoint will result in more
corrosion, as there is water separation. This results in water
wetting of the steel even if the water remains entrained in
the oil because of turbulent flow. The oil then still has an
inhibiting effect on the corrosion rate.
It has been found that there is a simple relationship between
the API gravity of the oil and the emulsion breakpoint. Data
were used from Craig (Corrosion Vol.54, 8, p.657) .
Reference:
B Craig, Predicting the Conductivity of Water-in-Oil Solutions, Corrosion Volume
54, 8, p. 657 1998.
C. de Waard, L. Smith, P. Bartlett and H. Cunningham, Modelling Corrosion Rates
in Oil Production Tubing, Eurocorr 2001, Paper 254.
C. de Waard, L. Smith and B. Craig, The Influence of Crude Oil on Well Tubing
Corrosion Rates, NACE Corrosion 2003, Paper 03629.
C. de Waard and U. Lotz, Prediction of CO2 Corrosion of Carbon Steel, Working
Party Report on Predicting CO2 corrosion in the oil and gas industry, European
Federation of Corrosion 1994.
J. Cai, S. Nesic and C de Waard, Modeling of Water Wetting in Oil-Water Pipe
Flow, NACE Corrosion 2004, Paper 4663.
Condensation of Water
The amount of water inside the pipe or tubing is
recalculated for every point along the length. Use is made
of a computerised graph from McKette and Wehe (Hydroc
Proc Aug 1958) of gas temperature vs. water content of
natural gas, with gas pressure as parameter. This changes
liquid hold up and liquid velocities and water cut along the
pipe length or up the height of the tubing. Gas temperature
and water content will not always be in equilibrium at high
flow-rates: this effect is outside the scope of ECE.
When glycol is added for hydrate or corrosion control in a
pipe, the amount of condensed water is modified as function
of the glycol injection rate.
ECE can be used to estimate the total amount of condensed
water from gas at the outlet by subtracting the water at
inlet rate (Throughput page ) from that at the outlet
(Details page).
Top of Line Corrosion
When there is a stratified flow pattern in a flowline, there is
the potential for Top-of-Line Corrosion. This is corrosion
attack on the upper part of the internal pipe surface in
contact with the gas phase, in contrast to attack on the
lower part in contact with the bulk liquid water phase. In
sweet conditions, severe Top-of-Line corrosion is typically
associated with high temperature gradients and high rates of
water condensation on the pipe walls. Note that Top-of-Line
Corrosion includes the whole surface in contact with the gas
phase, not just the 12 clock position.
The predicted Top-of-Line corrosion rate is proportional to
the rate of condensation of water from the gas (per unit area
of pipe wall) and the maximum Fe concentration in water at
the particular conditions of pressure, temperature and gas
composition. In physical terms, this expresses the maximum
rate at which water can remove iron ions from the pipe wall
as it condenses and then runs-off down to the bulk liquid
phase at the bottom of the pipe. This limits the potential rate
of corrosion of the pipe wall.
Reference:
Stein Olsen, Arne Dugstad, Corrosion under Dewing Conditions, NACE Corrosion
1992, Paper 472
Rolf Nyborg, Arne Dugstad, Top of Line Corrosion and Water Condensation Rates
in Wet Gas Pipelines, NACE Corrosion 2007, Paper 07555.
Corrosion Inhibition
Corrosion inhibitors, when carefully selected and
conscientiously applied, can give a significant reduction of
the corrosion rate. In ideal situations, well-chosen inhibitors
can achieve efficiencies of 99%.
References:
B.F.M. Pots and E.L.J.A. Hendriksen, CO2 corrosion under scaling conditions –
The special case of top-of-Line corrosion in wet gas pipelines, NACE Corrosion
2000.
Flow Patterns
Complete modelling of flow patterns in multi- phase flow is
an extremely complex problem, requiring knowledge of
many parameters which in practice are often not accurately
known, or which will in any case change over time or from
point to point in the tubing or flowline. Even in ideal
laboratory conditions, accurate prediction of flow patterns
has proved difficult. However, for the purpose of corrosion
modelling it is possible to group the possible patterns into
several broader classes: the fundamental distinctions are
between annular-mist flow, slug and bubble type flow
patterns, and (for flowlines) stratified, nonsymmetrical flow
patterns. ECE uses flow pattern regimes based on a
simplified version of the scheme of Petalas and Aziz.
Additionally, there is a Liquid Full regime.
Reference:
N. Petalas and K. Aziz, A Mechanistic Model for Multiphase Flow in Pipes,
Stanford University, 1998.
Glycol Injection
A special form of inhibition consists of the injection of
concentrated glycol in flowlines carrying wet natural gas
without formation water production. The glycol acts in two
ways:
Reference:
Russell et al, Choosing Better API RP 14E C Factors for Practical Oilfield
Implementation, NACE Corrosion 2011, Paper 11248.
Particle Erosion
The Tubing Erosion Predictor model is a slightly simplified
implementation of the smooth straight pipe and bend
models from DNV-GL RP O501:2015 “Managing sand
production and erosion”. The tool is intended for a first –
pass assessment or exploratory modelling. For detailed
assessment, reference to the full DNV-GL Code is
recommended.
The substrate material properties are for Carbon Steel.
The particle correction factor is fixed at 1 (worst case
assumption). Accurate information on the particle size
distribution and density is needed to calculate this
parameter and this is very often not available. Fixing this
value gives an upper bound result in terms of the RP O501
model.
The erosion values are calculated with the smooth straight
pipe formula and also with the pipe bend formula using the
radius of curvature from the tubing deviation profile. The
largest of these two values is reported.
The other necessary data for erosion calculation including
pipe dimensions and fluid flow velocities are calculated from
the inputs in ECE such as pressure, temperature, flow rates
etc.
Note that there is no interaction between the particle
erosion model and corrosion model, and any synergistic
effects that might occur are not covered. The corrosion
model removes the protective effect of scale and sulphide
filming at velocities above the API 14E erosional limit (see
“Erosion –corrosion”) .
In practice, to produce significant particle erosion rates in
tubing (essentially straight, smooth pipe) requires rather
extreme conditions of flow velocity and particle loading.
Reference: DNV-GL RP O501:2015 “Managing sand production and erosion”
Risk of Failure
The corrosion prediction models used in ECE have a limited
accuracy. The formulas used for CO2 corrosion prediction
give a standard deviation of about 25% for the corrosion
rate over their validated ranges, which means that there is
a chance of almost 16% that the actual corrosion rate is
outside the range ± 25%, assuming the statistics for a
normal distribution apply. Anyone who has been involved in
practical corrosion rate measurements in the laboratory or
the field will also appreciate that actual measurements on
replicate coupons or at equivalent positions can sometimes
vary by at least this much, often without a clear reason.
ECE calculates a normal distribution curve around the
maximum corrosion rate (truncated at zero corrosion rate)
and converts this to an accumulated risk of failure by
dividing into the wall thickness and integrating over time.
This yields a curve for the accumulated risk of failure vs
time: the time to reach a 50% risk of failure corresponds to
the nominal value of the maximum corrosion rate. Longer
exposure of the pipe or tubing will increase the risk of
failure, until finally a point is reached where failure is
almost certain.
In the presence of H2S there is a risk that the protective
sulphide layer on the steel is disturbed, and that localised
pitting corrosion occurs. The rate of penetration at these
pits are often equal to the CO2 corrosion rate. This is
accounted for in the risk of failure prediction by adding an
arbitrary 25% chance that the corrosion rate is based
entirely upon the localised pitting corrosion rate. The
standard deviation for the resulting prediction is larger (=
less certain) and has been set to 30%. When H2S is
present, the risk of loss of protection of the sulphide layer
shows up as a plateau early in the life in the accumulated
risk curve, when, of course, the CO2 corrosion rate is high
enough to show the effect.
Acetic Acid
Natural gas can contain small amounts of vapour of organic
acids, notably acetic acid. In view of the high solubility in
water, this can lead to concentrations of dissolved acetic
acid in condensed water, which can be significant in
increasing the corrosion rates to higher values than with
CO2 only. This is particularly noticeable in increasing the top
of the line corrosion rates since in such condensing
conditions the local environment is not influenced by
alkaline constituents like dissolved carbonates.
It is customary to report the acetic acid or acetate
concentration dissolved in the water, rather than the partial
pressure (in contrast to the case of CO2). If dissolved acetic
acid is detected in the field, the effect on corrosion rate can
modelled by changing the default value for this acid from
zero.
The action of dissolved acetic acid has been shown to be
analogous to that of carbonic acid: the undissociated acetic
acid is directly reduced at the metal's surface in addition to
the reduction of the undissociated carbonic acid. This
modifies the Vm term in the corrosion rate formula , and
causes the larger part of the increase in corrosion rate.
Guidance on Accuracy of
Prediction
Summary of Application
Limits