Professional Documents
Culture Documents
Paper No.: Effect of Soil and Disbondment Configuration On CP Penetration Into Coating Disbondment
Paper No.: Effect of Soil and Disbondment Configuration On CP Penetration Into Coating Disbondment
Paper No.: Effect of Soil and Disbondment Configuration On CP Penetration Into Coating Disbondment
11023
ABSTRACT
Tests were performed to investigate the effect of soil and disbondment configuration on CP penetration
into coating disbondment. An innovative experimental setup was employed to measure the pH and
potential of pipeline steel under a disbonded coating without disturbing the environment inside the
disbondment. It was revealed that CP penetration was dependent on CP level, environment inside the
disbondment, and distance from the holiday. CP penetration increased with increasing CP level, and
decreased with increasing pH and distance from the holiday. For a circular FBE coating disbondment,
the existence of clay soil in the solution acted as a physical barrier for OH- generated inside the
disbondment to diffuse out, and lead to a very alkaline environment around the holiday area, i.e., pH 14.
The presence of soil would cause an inhibiting effect to CP penetration. Majority of CP current was
consumed at the holiday and vicinity, and only a very small portion of CP current could reach beyond 10
mm into the FBE and HPPC coating disbondment even at CP level of -1126 mVSCE. CP current could
reach deeper into a narrow tunnel-shaped disbondment than into a circular-shaped disbondment with
similar conditions, i.e., similar sizes of holiday and disbondment gap. Tunnel-shaped coating
disbondment was subject to hydrogen accumulation inside the disbondment. In particular, HPPC coating
disbondment had a higher tendency to trap hydrogen gas than FBE coating disbondment. The trapped
hydrogen gas could effectively block the CP current from penetrating into the disbondment. The critical
parameters required for the occurrence of near neutral pH SCC, i.e., near neutral pH and potentials close
to Ecorr, could be achieved inside the tunnel-shaped HPPC coating disbondment under elevated CP levels
of -926 mV and -1126 mV due to the presence of trapped hydrogen gas.
Key words: CP penetration, coating disbondment, clay soil, disbondment configuration, OH-, hydrogen
accumulation, trapped hydrogen gas
The most effective method to mitigate corrosion on the external surface of a buried pipeline was to utilize
a protective coating supplemented by cathodic protection (CP). Ideally, these two systems should work
together so that if the coating is disbonded or has defects allowing electrolyte to contact the pipe steel
surface, the CP system would continue to function and provide corrosion protection to the pipeline.
However, the success of this approach greatly depends on the nature of coating failures. Corrosion
protection to the pipe with coating failures can only be achieved if sufficient CP current is able to reach
the exposed pipe steel.1-5 For instance, if adequate CP current is able to penetrate into a coating
disbondment, then corrosion related damages may be prevented. Otherwise, the exposed pipe steel can
be susceptible to corrosion and environmentally assisted cracking.
The extent of CP penetration into coating failures is associated with many factors such as coating
disbondment dimension, solution composition and conductivity, and coating type.1,6-9 It was observed that
CP was less effective to reach into coating disbondment as the disbondment became tighter, i.e. the
height of the gap between the coating and steel substrate decreased.1,6,9 CP would penetrate further into
the coating disbondment in solution with higher electrical conductivity.1,7,8 Jack et al.1 detected that CP
could only penetrate into disbondments with a relatively short distance, i.e., no more than 10 cm in ground
water with conductivities in the range of 0.5 to 5 mS/cm (equivalent to a resistivity range of 200 to 2000
Ω∙m). Ground water containing Ca2+, Mg2+, and carbonate ions could affect CP penetration and the
environment inside the disbondment by forming mineral deposits, and these deposit scales formed on
the top of the opening to the disbondment would act as barriers to CP penetration and alkalinity
migration.1
The available literature on CP penetration into coating disbondment predominantly employed
experimental arrangement with insulating polymer materials as pipeline coating alternative.6-9 In these
arrangements the outer surface of the disbondment was not exposed to solution , and CP could access
the disbondment only through the opening of the disbondment. In the real situation, for buried pipelines,
the coating outer surface is intimately in contact with soil and likely groundwater. CP and corrosive
species in the soil outside the coating disbondment can be possibly involved in the CP penetration and
mass transfer processes, and hence can impact the chemistry inside the disbondment.
This paper was a continuation of a previous study the focus of which was to examine the effect of different
pipeline coatings, namely, field applied two-part epoxy, fusion bonded epoxy (FBE), and high
performance powder coating (HPPC), on CP penetration into a circular-shaped coating disbondment.10
The intention was to investigate the effect of existence of soil in ground water and coating disbondment
configuration on CP penetration into coating disbondment.
EXPERIMENTAL PROCEDURE
Detection probes
Each detection probe comprises a home-made Sb/Sb2O3 pH electrode and an Ag/AgCl (0.1M KCl in 4%
agar) reference electrode. The preparation of the Sb/Sb2O3 and Ag/AgCl reference electrodes was
described elsewhere.10
Coating disbondment and test cell design
The details about the design and preparation of a circular-shaped disbondment was described elsewhere,
Figure 1(a).10 The circular-shaped coating disbondment was employed in the test with FBE coating and
soil slurry. The designated disbondment area located in the center of the steel panel was left untouched
with a diameter of 130 mm. The four embedded detection probes were located at 10 mm, 20 mm, 35
mm, and 50 mm, respectively, to the holiday. The probes were labeled as #1, #2, #3, and #4 in sequence
based on an increasing order of distance between the probe and the holiday. Four spacers were utilized
to control the depth/height of the disbondment to be 1mm.
The tunnel-shaped disbondment, Figure 2(a), was fabricated with FBE or HPPC coating with a dimension
of 160 mm x 20 mm x 1 mm. A rectangular spacer ring was glued to the steel panel to define the area
and depth/height of the disbondment. The holiday with a size of 3-mm-diameter was positioned at one
end of the disbondment. The five detection probes were located at 10 mm, 30 mm, 60 mm, 100 mm, and
140 mm to the holiday, and were numbered as #1, #2, #3, #4, and #5 , respectively. The preparation of
the tunnel-shaped coating disbondment was similar to that of the circular-shaped one and was
documented elsewhere.10 Due to the fact that borosilicate glass pasteur pipettes (with the small tip of
around 1mm in diameter) were used as the holders for the Ag/AgCl reference electrodes, the detection
probes were rather fragile. Probe #3 embedded in the tunnel-shaped FBE and Probe#4 embedded in the
tunnel-shaped HPPC coating disbondment were damaged during assembling. As a result, no data were
available for these two probes.
Figure 1(b) and
Figure 2 (b) show the schematic diagram of the experimental arrangement inside the coating
disbondment and test cell. The two setups were almost identical except for the location of the holiday
and the placement of the counter electrode. The horizontal placement of counter electrode was
intended to make the distribution of the CP current uniform if there was any current directly going
through the disbonded coating. The containment vessel with lid without bottom was constructed from 5
mm thick acrylic sheets. The acrylic vessel was sealed on top of the coating disbondment using RTV
silicone. Each test was performed with ~1000 ml NS4 solution. To ensure that the coating disbondment
would be filled with solution, the disbonded area was gently tapped with a glass rod to force the trapped
air out prior to the test. A 7-mm-diameter graphite rod and a SCE served as counter electrode (CE) and
reference electrode (RE), respectively, to allow the application of CP to the steel panel. The solution
was purged with 5% CO2 gas prior to and throughout the test to maintain a neutral pH of 7.0 ± 0.2 in
the bulk cell.
(a) (b)
Figure 1: Schematic of the experimental setup for the circular-shaped disbondment, (a) top view
of the arrangement of detection probes inside the coating disbondment; (b) front view of the
test cell
(a) (b)
Figure 2: Schematic of the experimental setup for the tunnel-shaped disbondment, (a) top view
of the arrangement of detection probes inside the coating disbondment; (b) front view of the
test cell.
(a) (b)
-1126 mV
-926 mV
-776 mV
(c)
Figure 3: Measurements obtained from the test with circular FBE disbondment in soil slurry, (a)
transient current; (b) potential; and (c) pH.
-926 mV
-776 mV -926 mV
(c)
Figure 4: Measurements obtained from the test with circular FBE (350 µm in thickness)
disbondment in NS4 solution, (a) transient current; (b) potential; and (c) pH.10
Figure 5(a) – (d) show the potential values of the pipeline steel at different probe locations inside the
FBE disbondment submerged in soil slurry under CP and no CP conditions. The degree of CP
penetration into the coating disbondment was estimated using the potentials difference between these
two CP conditions which was denoted as polarization potential, Epola, in the previous study.10 Due to the
identical Epola behavior at Probe#3 compared to that at Probe#4, only the data obtained at Probe#4
were shown in Figure 5. Unfortunately, no Epola data were available from the test with circular-shaped
FBE (350 µm) coating disbondment in NS4 solution for comparison. At the holiday, Figure 5(a), the Epola
values were obvious at the elevated CP levels, i.e., Epola were around 30 mV and 150 mV at CP levels
of -926 mV and -1126 mV, respectively. At CP of -776 mV, the corrosion potential of the steel panel,
Ecorr, at the holiday quickly approached -775 mV from its original value of -735 mV before the
application of CP due to the fast established alkaline environment. As a result, a negligible potential
difference, namely, little CP penetration, was detected at the holiday location at CP of -776 mV. At the
location of Probe #1, small Epola values were observed at the early stage of CP applications of -926 mV
and -1126 mV, i.e., 10 ~ 15 mV. After the high pH environment was established and stabilized inside
the disbondment, the potential difference disappeared and no CP penetration was detected. Negligible
Epola and CP penetration at locations of Probe #2, #3 and #4 were detected under all CP conditions. It
was implied that the penetration of CP was dependent on CP level, environment inside the
disbondment, and distance to the holiday. CP penetration decreased with decreasing CP level, and
with increasing pH and distance from the holiday. The majority of CP was consumed at the holiday
area, only a very limited CP penetration could be seen inside the FBE coating disbondment. The limited
CP penetration was present in areas adjacent to the holiday and would disappear as the high pH
-776 mV
-926 mV
-1126 mV
(a) (b)
(c) (d)
Figure 5: Potential measurements with CP and without CP inside the circular-shaped FBE
disbondment in soil slurry at, (a) coating holiday; (b) Probe #1; (c) Probe #2; and (d) Probe #4.
(a) (b)
-1126 mV
-926 mV
-776 mV
(c)
Figure 6: Measurements obtained from the test with tunnel-shaped FBE coating disbondment in
NS4, (a) transient current; (b) potential; and (c) pH.
©2018 by NACE International.
Requests for permission to publish this manuscript in any form, in part or in whole, must be in writing to
NACE International, Publications Division, 15835 Park Ten Place, Houston, Texas 77084.
The material presented and the views expressed in this paper are solely those of the author(s) and are not necessarily endorsed by the Association.
10
-776 mV
-1126 mV
-926 mV
(a) (b)
(c) (d)
Figure 7: Potential measurements with CP and without CP inside the tunnel-shaped FBE coating
disbondment in NS4 at, (a) coating holiday; (b) Probe #1; (c) Probe #2; and (d) Probe #5.
-926 mV
-1126 mV
-776
mV
(a) (b)
(c)
Figure 8: Measurements obtained from the test with tunnel-shaped HPPC coating disbondment
in NS4, (a) transient current; (b) potential; and (c) pH.
©2018 by NACE International.
Requests for permission to publish this manuscript in any form, in part or in whole, must be in writing to
NACE International, Publications Division, 15835 Park Ten Place, Houston, Texas 77084.
The material presented and the views expressed in this paper are solely those of the author(s) and are not necessarily endorsed by the Association.
12
Figure 9(a) to (d) show the potential values of the pipeline steel at different locations inside the tunnel-
shaped HPPC disbondment in NS4 under CP and no CP conditions. The data obtained at Probe #3
were similar to those at Proble#5, and thus were not included in the paper to avoid duplication. Similar
to other tests, the greatest Epola values were always detected at the holiday area. Trivial CP penetration
was detected at all three CP levels even at Probe#1 before the removal of hydrogen gas from the
disbondment, which was consistent with the current, potential, and pH data shown in Figure 8. As
discussed previously, this should be attributed to the blocking effect of hydrogen gas to CP current.
Modest Epola values, i.e., 74 mV and 33 mV, were detected at CP of -1126 mV at Probe#1 and #2,
respectively, upon the removal of the hydrogen gas on Day 145. Then the values of Epola quickly
dropped to around 20 mV and 10 mV at Probe#1 and #2, respectively. Negligible Epola was obtained
beyond Probe#2 throughout the test regardless of the CP level and the removal of hydrogen gas
indicating little CP current was present at locations further than 30mm into the disbondment.
-776 mV -926 mV
-1126 mV
(a) (b)
(c) (d)
Figure 9: Potential measurements with CP and without CP inside the tunnel-shaped HPPC
coating disbondment in NS4 at, (a) coating holiday; (b) Probe #1; (c) Probe #2; and (d) Probe #5.
CONCLUSIONS
Three tests were performed with different coating disbondments and test solutions to investigate the
effect of disbondment configuration and soil on CP penetration into coating disbondment. The
conclusions are,
1. In general, CP penetration was dependent on CP level, environment inside the disbondment, and
distance from the holiday. CP penetration increased with increasing CP level, and decreased with
increasing pH and distance from the holiday.
©2018 by NACE International.
Requests for permission to publish this manuscript in any form, in part or in whole, must be in writing to
NACE International, Publications Division, 15835 Park Ten Place, Houston, Texas 77084.
The material presented and the views expressed in this paper are solely those of the author(s) and are not necessarily endorsed by the Association.
13
2. For a circular FBE coating disbondment, the existence of clay soil in the solution acted as a
physical barrier for OH- generated inside the disbondment to diffuse out, and lead to a very
alkaline environment around the holiday, i.e., pH 14. The presence of soil would cause an
inhibiting effect to CP penetration.
3. Majority of CP current was consumed at the holiday and vicinity, and only a very small portion of
CP current could reach beyond 10 mm into the FBE and HPPC coating disbondments even at CP
level of -1126 mVSCE. CP current could reach deeper into a narrow tunnel-shaped disbondment
than into a circular-shaped disbondment with similar conditions, i.e., similar sizes of holiday and
disbondment gap.
4. Tunnel-shaped coating disbondment was subject to hydrogen accumulation inside the
disbondment. The trapped hydrogen gas could effectively block the CP current from penetrating
into the disbondment. The critical parameters required for the occurrence of near neutral pH SCC,
i.e., near neutral pHs and potentials close to Ecorr, could be achieved inside the tunnel-shaped
HPPC coating disbondment under elevated CP levels of -926 mV and -1126 mV due to the
presence of trapped hydrogen gas.
ACKNOWLEDGEMENT
This project was partially funded by the Canadian Federal Interdepartmental Program of Energy R&D.
REFERENCES
1. Jack, T.; Van Boven, G.; Wilmott, M.; Sutherby, R.L.; and Worthingham, R.G., “Cathodic protection
potential penetration under disbonded pipeline coating” MP 33 (1994): p. 17.
2. J. Been, F. King, Y. Lin, “The role of coating in the generation of high- and near-neutral pH
environments that promote environmentally assisted cracking,” CORROSION/2005, Paper No. 05167
(Houston, TX: NACE, 2005).
3. F.M. Song, N. Sridhar, “Chemistry and corrosion rates under pipeline disbonded coating with or
without cathodic protection,” CORROSION/2007, paper no. 07118 (Houston, TX: NACE, 2007).
4. A. Eslami, B. Fang, R. Kania, B. Worthingham, J. Been, R. Eadie, W. Chen, “Stress corrosion
cracking initiation under the disbonded coating of pipeline steel in near-neutral pH environment”
Corrosion Science 52 (2010): p. 3750.
5. A. Eslami, R. Kania, B. Worthingham, G.V. Boven, R. Eadie, W. Chen, “Corrosion of X-65 pipeline
steel under a simulated cathodic protection shielding coating disbondment,” Corrosion 69, 11 (2013): p.
1103.
6. R.R. Fessler, A.J. Markworth, R.N. Parkins, “Cathodic protection levels under disbonded coatings,”
Corrosion 39, 1 (1983): p. 21.
7. K. Fink, J.H. Payer, R. Savinell, “Mitigation of corrosion by modification of the environment beneath
disbonded coatings on pipelines,” CORROSION/1993, Paper No. 578 (Houston, TX: NACE, 1993).
8. R. Brousseau, S. Qian, “Distribution of steady-state cathodic currents underneath a disbanded
coating,” Corrosion 50, 12 (1994): p. 907.
9. M.C. Yan, J.Q. Wang, E.H. Han, W. Ke, “Electrochemical measurements using combination
microelectrode in crevice simulating disbanded of pipeline coatings under cathodic protection,”
Corrosion engineering, science, and technology 42, 1 (2007): p. 42.
10. L.Yan, J.P. Gravel, M. Arafin, “ Penetration of Cathodic Protection into Pipeline Coating
Disbondment,” CORROSION/2017, Paper No. 9046 (Houston, TX: NACE, 2017).
11. NACE SP 0169-2013, “Control of external corrosion on underground or submerged metallic piping
systems,” (Houston, TX: NACE)