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Two Years After First Oil Paraffin and Scale Flow Assurance Management
Lessons Learned
Jonathan J Wylde - Clariant (Canada) Inc.
Abstract
This paper describes the evaluation of paraffin and scale risk management based on real production samples, and how this
differed to the assumptions made during the basis of design.
The production facility has two unmanned tiebacks with a field total of just under 20 wells. For first oil the paraffin and scale
management strategy, like most of the flow assurance strategy, was based on pre-production samples. Two years after first
oil, almost all the wells were sampled the first such exercise of its kind gathering large and representative chemical free
crude oil and produced water.
Produced water samples were analyzed enabling a system-wide scale review for production wells, departing pipelines and
major processing vessels and equipment. Some scale had already been observed in the process, in the hydrocyclones and heat
exchangers, and this evaluation helped to highlight the other key risk areas and develop appropriate mitigation strategies
not based on pre-production data and samples. This aided the operator in instigating a more robust scale inhibitor injection
strategy, in particular for the subsea in-field flow lines.
The areas identified as having a paraffin deposition risk in the field were the fluids arriving from the subsea tiebacks where
the arrival temperatures were lower than the cloud points. Cold finger testing identified that greater than 60% inhibition
efficacy was realized when 10 to 50 ppm of the incumbent wax inhibitor was used.
Details are given on some of the shortcomings in the chemical injection system, capturing the lessons learned in control of
wax and scale inhibitor distribution through the subsea injection system. Information is given on how this was countered
using the most efficient and cost effective chemical mitigation strategy. Practical advice is then offered on how to better
interpret pre-production samples to better predict and design flow assurance strategies prior to first oil.
Introduction
The field is an oil and gas asset development located in the Gulf of Mexico in water between 85 to 190 feet deep. It produces
oil and gas with associated condensate. The designed processing capacity of the facility is 100 MBOPD and 280 MMcf/d of
gas. The produced oil has a gravity between 28 to 34 API, and is low in sulfur and acid. The design anticipated the wells to
produce up to 20% BS&W in late field life. Based on laboratory results, asphaltene deposition was not expected to be a
concern; however, the pre-production crude samples had over 6% paraffin with a cloud point as high as 82F. The crude oil
export specification is 0.5% BS&W, and a TVP of 11.0 psia.
The basis of design was for a phased field development:
Phase 1 (Years 1 to 4): Oil production and full gas re-injection. This includes installation of a central production
facility with three satellite wellhead platforms. Oil is exported to an onshore terminal via pipeline.
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Phase 2 (Years 5 to 10): Early gas sales may be considered which occurs concurrently with oil production and gas
re-injection. Gas sales will be a potential 150 to 200 MMcf/d, and will be exported as wet or dry gas via a new
purpose-built gas export line.
Phase 3 (Late Field Life / Gas Sales): Gas sales of 250 to 350 MMcf/d to field depletetion. Oil production is
expected to decline to unsustainable levels and therefore no gas re-injection will be required.
A central production and processing platform including power generation, utility, flare, life support systems and
living quarters.
Three wellhead platforms (WHP) two remote and one bridge linked to the central processing platform.
An export oil pipeline.
Intra-field production flow lines connecting the WHPs to the central platform, and intra-field gas injection flowlines
from the central platform to the gas injection wells on the various WHPs.
Figure 1 shows the field architecture layout drawing giving a schematic overview of the development, and Figure 2 shows a
simplified schematic of the liquid processing equipment on the central platform.
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Lessons Learned After Flow Assurance Re-Evaluation Two Years Following First Oil
Paraffin / Wax Flow Assurance Post-First Oil Assessment
Samples were taken from all the online wells during an extensive campaign in December of 2007 with 11 of the online
wells sampled. This was the first such sampling campaign of its kind since first oil, and after two full years of production
provided the most representative data gathered for the field.
Experimentation was performed on these samples to evaluate waxing tendency. This was combined with process information
gathered during a detailed offshore platform survey to determine the overall waxing risk to the process. Further, an
observational check of the mitigational strategies was assumed during the project phase. Most importantly, the
experimentation aimed to determine whether the current 10 ppm of wax inhibitor injection was sufficient to control wax
deposition based on the properties of individual and commingled crude oil samples. Cold finger tests were performed to
evaluate the performance of products on commingled samples blended in such a way to mimic the highest risk waxing
areas.
The physical properties of the crude oils have been summarized in Table 4. Various analytical techniques were used to
determine the wax and asphaltene content of the crude oil as well as the WAT and pour point. The WAT results differed
significantly from the basis of design measurements all being considerably higher, i.e. worse in terms of flow assurance
risk. A previous study in September 2005 showed the WAT to be 122F for WHP 2 and 111F for WHP 3. It would seem
that the WAT has increased with time this is not uncommon as initial production has more light ends (associated with the
gas cap) and once these deplete, the heavier crude oil displays a higher waxing tendency.
The asphaltene content measured in these post-first oil samples was similar to that of pre-production samples but
significantly the wax content was lower this was hypothesized to be because there was significant contamination of the preproduction samples, potentially with drilling and completion fluids. Pour point measurements showed the crude did not have
a gelling propensity, as no pour point above 10F was measured.
At the time of testing, the field treatment was to inject 10 ppm of a wax inhibitor to the WHP 2 and 3 subsea headers prior to
the produced fluids entering the in-field subsea flow lines. The testing focus thus shifted on more field representative cases
where mixtures of the individual crude samples were made (based on production rates) according to the following ratios:
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dispersive x-ray analysis (EDX) and x-ray diffraction (XRD). The drying and ashing showed some minor aqueous and
hydrocarbon components to the samples but the majority was inorganic. The EDX results have been summarized in Table 9
and show that all the samples were dominated by calcium and calcium carbonate, with the exception of one electrostatic
heater treater sample which also had 12 to 13% of barium suggesting deposition of barium sulfate. Siliceous material was
detected in all samples indicated by silicon composition up to 17%.
The origin of the calcium carbonate material in the process is unclear. Two hypotheses seemed plausible: In-situ origin
caused by scale formation of the produced water due to depressurization through the process; or drilling weighting agents
returning from the clean-up of newly drilled wells. This latter hypothesis was proposed because particle size distribution
analysis on one of the scale deposits showed it to be similar to the drilling mud slurry utilized for the well.
An extensive modeling exercise was performed based on sampling campaign water analyses, which has been summarized in
Table 10. The results of the scale modeling suggested:
Production wells: At tubing head temperatures and pressures, barite scale would form for WHP 1, Well 1 produced
water due to the higher sulfate content; injection of scale inhibitor was recommended. Calcite scale would form for
WHP 3, Well 2 and WHP 1, Well 1 produced water, and likewise scale inhibitor injection was recommended. All
waters collected from production wells showed siderite scale potential due to high bicarbonate contents.
Departing in-field pipelines: WHP 1 flowline had a barite and calcite precipitation challenge, thus scale inhibitor
injection was recommended. All the departing pipelines showed siderite scaling tendency.
CPP facilities: the HGOR separator exhibited a barite and calcite precipitation challenge, and scale inhibitor
injection was recommended.
These results validated the observation of mild calcite scale in the process system. Small amounts of barite and siderite were
also speculated because of existence of elemental barium, iron and sulfur in the scale samples.
Dynamic Scale Loop (DSL) testing was performed on a composite mix of the water chemistries at 100F and 140F to
represent topside conditions. The DSL testing did not yield a scaling blank after 17 hours. The most severe waters, WHP 1,
Well 4 and WHP1, Well 1, were chosen for secondary testing at 140C yet still did not scale in a blank test after more than
eight hours. It is likely that the scale forming in the field is doing so slowly and, therefore, it is challenging to evaluate in the
laboratory.
The strategy adopted was to not inject scale inhibitor until more evidence of scale formation was apparent. This was
determined to be robust because it also comprised regular field observations and monitoring. The scale samples that had been
recovered thus far were during routine maintenance operations and had not themselves caused process upsets or blockages. It
was sustainable to continue to remove scale deposits during routine operations this would continue until the burden of
removal became too great.
The wax content of the crude oils tested ranged from 1.38 to 2.90 wt%, with the WAT varying from 136 to 144F
and the pour point not greater than 9F.
WHPs 2 and 3 were identified as having a wax deposition risk, as the fluid arrival temperatures at the Central
Platform were lower than the WATs.
At 10, 50 and 100 ppm incumbent wax inhibitor, there was little or no effect observed on the WATs and pour points
of any crude oil mixtures tested.
Cold finger wax inhibition testing identified that greater than 60% inhibition efficacy was realized when 10 ppm of
the incumbent wax inhibitor was used for WHP 2 crude oil, and when 50 ppm was used for WHP 3 crude oil.
The results of this study differed significantly to the basis of design. The WATs were lower and the wax content
higher. The difference in WATs can be ascribed to later production being richer in heavier end components with
pre-production samples having more light ends associated with the gas cap. The difference in wax content was most
likely due to contaminated samples.
It was recommended to ensure injection of 10 ppm of the wax inhibitor into the commingled fluids departing WHP 2 to the
Central Platform to protect the intra-field subsea flowline. For WHP 3, 50 ppm of wax inhibitor injection was recommended
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to be injected into the departing fluids. However it was acknowledged that there was little or no control on the distribution of
wax inhibitor injected due to the flow indicators being out of range. Therefore, it was required to inject 50 ppm of wax
inhibitor to both WHP 2 and 3, i.e. based on gross oil production from both tiebacks, to ensure adequate distribution of wax
inhibitor to the required locations this assumed that there was a similar distribution of wax inhibitor to all injection points,
validated to a degree by calculation.
The scale deposition propensity determined through the post-production sampling exercise did not yield significant
differences between the basis of design assumptions and the post-first oil case. The following conclusions can be drawn:
The basis of design water compositions, whilst less saline overall, did have a higher concentration of scaling ions
than those measured during the well sampling exercise. It is acknowledged however, that water of condensation
could be diluting the wellhead samples taken post-production.
The basis of design predicted scale formation in the process as well as downhole. To date, no scale has been
determined to have formed downhole but scale has been removed from the process.
Some barium (sulfate) has been observed in scale samples, but it is unclear whether this was due to in-situ
precipitation or was a result of drilling fluid contamination.
Consideration to the injection of scale inhibitor to prevent calcite scaling has been given; however, the strategy to
date has been to not inject, rather focus on monitoring process trends. This has been sustainable because of the
relatively low water production and low scaling potential. There is, of course, risk associated with this when scale
formation is known to be occurring, but routine monitoring can manage this risk.
A process acidization job has been evaluated and was based on glacial acetic acid injection.
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Table 1: Stock tank crude oil properties from the two different reservoir panels in the field development
Stock Tank Crude Oil Properties
COMPONENT
Wellhead Platforms
Wellhead
1 and 2
Platform 3
29.0
33.3
67 to 93
82 to 134
5.2
6.7
<10
52
0.98
0.55
0.64
0.41
2.8
1.06
API Gravity
Wax Appearance
Temperature (F)
Table 2: Pre-production water analysis results from different reservoir panels in the field development
COMPONENT
Wellhead
Platform 2
Wellhead Platform 1
Wellhead
(mg/L)
Platform 3
(mg/L)
Sodium, Na
5,600
5,820
6,010
7,680
44
43
56
56
49
156
306
150
23
26
50
10
30
20
60
6,568
8,558
8,865
12,592
Potassium, K
2+
Calcium, Ca
Magnesium, Mg
2+
2+
Barium, Ba
2+
Iron, Fe (Total)
-
Chloride, Cl
Bicarb., HCO3
(mg/L)
2,641
1,592
1,293
1,324
2-
180
968
283
331
7.70
7.47
7.47
7.09
Sulfate, SO4
Bromide, Br
pH
Wellhead
Platform 2
Wellhead
Platform 3
2,625
2,855
2,760
Wellhead P (psia)
450 to 1,160
450 to 1,160
450 to 1,160
170
170
170
110 to 130
110 to 130
110 to 130
Wellhead T (F)
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Table 4: Results of the crude oil wax appearance temperature, pour point, wax and asphaltene content testing on postfirst oil production samples
Sample Point
WHP 2
Well 1
WHP 2
Well 2
WHP 1
Well 1
WHP 1
Well 2
WHP 1
Well 3
WHP 1
Well 4
Asphaltene %
1.91
2.53
1.42
2.10
2.18
2.10
Wax %
2.90
1.38
2.40
1.92
1.70
1.87
WAT (F)
144
140
144
136
142
140
<5
<5
<5
<5
57
57
Sample Point
WHP 1
Well 5
WHP 3
Well 1
WHP 3
Well 2
WHP 3
Well 3
WHP 3
Well 4
Asphaltene %
2.38
1.00
1.71
2.10
1.13
Wax %
1.25
1.60
2.70
1.83
2.00
WAT (F)
144
136
140
144
144
<5
<5
<5
<5
69
Table 5: Results of the crude oil wax appearance temperature, pour point using 10 ppm of wax inhibitor (WI) on
representative WHP 2 and 3 fluids
Sample
Point
WHP 2
Blank
WHP 2
10 ppm
WI
WHP 2
50 ppm
WI
WHP 2
100 ppm
WI
WHP 3
Blank
WHP 3
10 ppm
WI
WHP 3
50 ppm
WI
WHP 3
100 ppm
WI
WAT (F)
144
144
140
140
136
136
136
136
Pour point
(F)
<5
<5
<5
<5
<5
<5
<5
<5
Dry Season F
Wet Season F
min
max
min
Max
77
83
80
86
66
73
84
78
87
131
69
86
73
87
197
66
82
71
85
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Table 7: Summary of the WHP 3 cold finger experiments using the incumbent
wax inhibitor at 10, 50 and 100 ppm
PPM
Mass (g)
% Inhibition
Comments
WHP 3 Blank
0.7680
Blank
10
0.4144
46.0
50
0.2704
64.8
100
0.2014
73.8
Table 8: Summary of the WHP 2 cold finger experiments using the incumbent wax inhibitor
at 10, 50 and 100 ppm
PPM
Mass (g)
% Inhibition
Comments
WHP 2 Blank
0.4561
Blank
10
0.1698
62.8
50
0.0932
79.6
100
0.0775
83.0
Table 9: Semi-quantitative EDX analysis result summary on all scale samples removed from the process
Element
C
O
Na
Mg
Al
Si
S
Cl
K
Ca
Fe
Ba
Electro Heater
Treater
Feb 29, 2008
0
12.45
0.51
0.46
1.90
7.89
2.87
1.52
1.10
54.53
3.63
13.04
Hydrocyclone
Feb 21, 2008
Hydrocyclone
Nov 14, 2007
Hydrocyclone K-liners
Nov 15, 2007
0
21.45
0
0
0.36
5.60
0.53
0
0
71.05
1.02
0
0
15.96
0.50
0.76
2.35
17.00
3.58
0.92
0.92
40.98
5.03
12.00
0
23.30
1.49
0
0.69
0
0
0
0
72.50
2.03
0
10
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Table 10: Produced water analyses from extensive post-first oil sampling exercise from wells across the field
WHP 3Well 1
WHP 3Well 2
WHP 3Well 3
WHP 2Well 2
WHP 1Well 5
WHP 1Well 3
WHP 1Well 4
WHP 1Well 1
Central
Plat.
(mg/L)
(mg/L)
(mg/L)
(mg/L)
(mg/L)
(mg/L)
(mg/L)
(mg/L)
(mg/L)
8,783
8,044
6,998
9,322
6,400
7,227
11,473
1,705
1,504
2.50
2.50
8.50
2.75
2.00
1.50
24.75
15.25
10.25
1.00
3.75
1.75
4.75
1.00
1.25
5.25
3.25
0.25
3.00
2.50
1.75
1.00
1.00
16.75
3.75
15.25
0.25
3.25
2.25
2.00
0.50
1.00
15.75
6.75
9.00
2.25
4.00
1.75
2.00
5.00
4.50
3.75
0.50
0.00
12,000
11,000
9,500
14,000
8,500
10,000
17,500
13,000
12,000
2,672
2,672
2,428
915
2,440
2,086
805
2,330
2,281
Sulfate, SO4
154
49
34
53
51
45
32
1,550
0.00
pH
8.8
8.5
8.4
8.6
8.5
8.5
7.0
7.9
7.3
Production Rate
(BWPD)
122
208
103
131
33
39
825
118
N/A
COMPONENT
Sodium, Na+
2+
Calcium, Ca
Magnesium, Mg
2+
2+
Barium, Ba
Strontium, Sr
2+
2+
Iron, Fe (Total)
-
Chloride, Cl
Bicarb., HCO3
2-
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11
12
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Wellhead Platform 3
CAN
Wellhead Platform 2
KAI 1
HP Separator
Wellhead Platform 1
KAI 2
HGOR
Separator
Oil Trim
Exchanger
IP Separator
Oil Heater
Produced Water
Hydrocyclone
LP Separator
Flotation Cell
Electrostatic
Heater Treater
To Skim Pile
Figure 2: Simplified schematic of the central processing platform equipment as well as how the wellhead
platform wells are manifolded
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13
Figure 3A: Scale precipitation modeling for Wellhead Platform 1 waters using a bottom hole temperature of 170F
and 2,625 psia and wellhead choke of 110F and 450 psia with all intermediate temperatures and pressures
Figure 3B: Scale precipitation modeling for Wellhead Platform 1 waters using a bottom hole temperature of 170F
and 2,625 psia and wellhead choke of 130F and 450 psia with all intermediate temperatures and pressures
Figure 4: Solids removed from the process plant. Electrostatic heater treater sample Feb 29, 2008 (left); hydrocyclone
Feb 21, 2008 (right)